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| ALEX. AGASSIZ.
Hibrary of the Museum
OF
COMPARATIVE ZOOLOGY,
AT HARVARD COLLEGE, CAMBRIDGE, MASS.
Founded by private subscription, in 1861.
Deposited by ALEX. AGASSIZ.
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INCLUDING
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VOL. XVI.—FIFTH SERIES.
PO
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‘¢ Onines res creatze sunt divine sapientie et potenti testes, divitiz felicitatis
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ex ceconomia in conservatione, proportione, renovatione, potentia majestatis
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a veré eruditis et sapientibus semper exculta; malé doctis et barbaris semper
inimica fuit.”—Linnaovs.
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00 Oo ...-.. . Lhe sylvan powers
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The Dryads come, and throw their garlands wild
And odorous branches at our feet; the Nymphs
That press with nimble step the mountain-thyme
And purple heath-flower come not empty-handed,
But scatter round ten thousand forms minute
Of velvet moss or lichen, torn from rock
Or rifted oak or cavern deep: the Naiads too
Quit their loved native stream, from whose smooth face
They crop the lily, and each sedge and rush
That drinks the rippling tide: the frozen poles,
Where peril waits the bold adventurer’s tread,,
The burning sands of Borneo and Cayenne,
All, all to us unlock their secret stores
And pay their cheerful tribute.
J. Taytor, Norwich, 1818.
CONTENTS OF VOL, XVI.
[FIFTH SERIES.]
NUMBER XCI.
I, On some Deep-sea and Shallow-water Hydrozoa. By Joun J..
QuricH, B.Sc. (Lond.), Natural History Museum. (Plates I. & IL)
II. Notes to the Australian Sponges recently described by H. J.
Carter, F.R.S. By Dr. R. v. LENDENFELD, in Sydney ..........
IIL. On the Teredo utriculus of Gmelin, with remarks upon other
Ship-worms. By Syitvanus Hanuey, F.LS. &. ..............
IV. Report on the Testaceous Mollusca obtained during a Dredging-
excursion in the Gulf of Suez in the Months of February and March
1869. By Rosert MacANpREw.—Republished, with Additions
and Corrections, by ALFRED Hanps Coons, M.A., Curator in Zoo-
logy, Museum of Zoology and Comparative Anatomy, Cambridge.—
Praia ble Peng Soo ako SOc fate coathes ane hy abe llgha’ cadice, ofasodlera alvlals wae ais
V. On Doratopteryx of Rogenhofer, a Genus of Moths allied to
Himantopterus. By AniHuR G. BUTLER, F.L.S., F.Z.8., &. ....
VI. On the Blue-helted Species of the Butterfly-genus Prothvé.
Bye RrHiR Go BUTLER HAS EA S566. 0. disci cess ee es
VII. Notes on Mesozoic Cockroaches. By SamurLt H. ScuppDER.
New Books:—The Birds of Lancashire. By F. 8. MircHeri.—
Memoirs of the Geological Survey of India. Palontologia
Indica, being Figures and Descriptions of the Organic Remains
procured during the Progress of the Geological Survey of India.
Series x. Indian Tertiary and Post-Tertiary Vertebrata. Vol.
UI. Parts 1-5. By R. Lypexxsr, B.A., F.GS., F.Z.S.—
Memoirs of the Geological Survey of India. Paleeontologia
Indica, being Figures and Descriptions of the Organic Remains
procured during the Progress of the Geological Survey of India.
Series iv. Vol. I. Part 4. The Labyrinthodont from the
Bijori Group. By R, LypEKKeEr, B.A., F.G.S., F.Z.8..... 65-
Page
ws
IV CONTENTS. ss
ets Page
A long-tongued Pteropine Bat from West Africa, by Dr. H. A.
Pagenstecher ; On the Mode of Development of Cantharis vesi-
catoria, by MOH. Beauregard, © ..:....!. eee eee 74
NUMBER XCII.
VIII. Remarks on the Geographical Distribution of the Lacertilia.
By GoASBOULENGER: (5 0006002 one 1d eet » lero nel eee 77
TX. Second List of Reptiles and Batrachians from the Province
Rio Grande do Sul, Brazil, sent to the Natural-History Museum by
Dr Ey you thernns: “By GA. BOwLENGER: | .55 1-0-1 eee 85
X. On the “Tag” of Celopleurus Maillardi, Mich. By Prof. P.
Mar Tine DUNCAN, BUR Se icici cag cn eo cis Sear ee nis 6g eee 88
XI. Remarks on the Ccelenterate Nature of the Sponges. By
RW Want MAR SHEAR ie rier. Felege tole vis olelos ie. «intel «esac ee 90
XII. On some Points in the Morphology of the Echinoderms, and
more especially of the Crinoids. By P. Hersert CarpEnter, D.Sc.,
IE R:S.; Assistant) Master at Eton College <. 2...) J 15.5 saeeeee 100
XIII. Deseription of a new Species of the Zetides Section of
Rapiliom Dy, EM GORE S.A oe aoe. ioraee eee 120
XIV. A new Frog (Rana sternosignata) from Sind. By James
A. Murray, Curator of the Kurrachee Municipal Museum........ wb,
XV. Description of two new Curculionide (Ectemnorhinus) from
Marion Islands. By CHARLES O. WATERHOUSE ..............0- 121
XVI. On the Relationship of Ulodendron, Lindley and Hutton, to
Lepidodendron, Sternberg; Bothrodendron, Lindley and Hutton ;
Sigillaria, Brongniart ; and Rhytidodendron, Boulay. By Rosrerr
iKapsron, EG:S: (Blates UE =Villl.) aro. tami eee 123
New Book :—Year-Book of the Scientific and Learned Societies of
Great Britain and Ireland; comprising Lists of the Papers read
during 1884 before Societies engaged in fourteen Departments of
Research, with the Names of the Authors. Compiled from
Official Sources. Second Annual Issue .........:.......... 139
Proceedings of the Dublin Microscopical Club .............. 140—149
Proceedings of the Geological Society .............eese se eeeeeee 149
On the Existence of a Nervous System in the Accelous Planarize and
of a new Sense-organ in Convoluta Schultzi, by M. Yves Delage;
The Nest of the Fifteen-spined Stickleback, by Prof. Karl
Mobius; F’reta ampulla, the Flask-Animalcule, by Prof. Karl
Mobius ; On Adamsia palliata, by M. Faurot; Note on “ Deep-
sea and Shallow-water Hydrozoa,” by J. J. Quelch, B.Sc.
(Gb Rese rene wn ea ALLE CAG ac 5.33 150—156
CONTENTS. Vv
NUMBER XCIII.
XVIL. On Phenicurus. By M. H. pp Lacaze-DuTHiers...... 157
XVIII. On the Relationship of Ulodendron, Lindley and Hutton,
to Lepidodendron, Sternberg ; Bothrodendron, Lindley and Hutton ;
Sigillaria, Brongniart ; Rhytidodendron, Boulay. By Roprrr Krp-
EUNICE oe foc8e 4 ile fcas eaeay Hoesia, og ehcunlatiny oh of op Sueno Soa araueteyay Voc oue as eeetons 162
XIX. Ona Variety of the Freshwater Sponge Meyenia fluviatilis,
auetiyarom Elorida. By H. J. Cantar, FURS, &e, ......-. 505: 179
XX. Diagnoses of new Species of Cephalopoda collected during the
Cruise of H.M.S. ‘Challenger.’—Part II. The Decapoda. By
Witiiam E. Hoyze, M.A. (Oxon), M.R.C.S., F.R.S.E., Naturalist
fombowaChalllenger’? Commission: 00.6062 .s ye cree eo eee eee time soe 181
XXI. New Species of Histerrde, with Synonymical Notes. By
Re TIEN MIM WIS: thnks dhs cTibra ais, soles oeimiale Sart « oF Saba eS aaa « 203
XXII. Critical Notes on Dr. Augustus Gruber’s “ Contributions to
the Knowledge of the Amaebe.” By Surgeon-Major WatL.icy,
New Books:—Australian Museum. Catalogue of the Australian
Hydroid Zoophytes. By W. M. Barz.—Elementary Text-Book
piimiomolosy. By NV. KIRBY. 22 c\cncscte ses cen 227—230
_ Proceedings of the Geological Society .................000., 230, 231
On a new State of Reticularian Rhizopods, by M. de Folin ; Descrip-
tion of a new Crustacean allied to Homarus and Nephrops, by
Sidney I. Smith; On a Crocodile-skull from the Tertiary De-
posits of Egeenburg in Lower Austria, by Franz Toula and
Jighemia AS ISG ae obonganconbo ose an npn. aae oa ce 232—236
NUMBER XCIV.
XXIII. Descriptions of two new Species of Araneidea. By the
Rey. O. P. Campripgr, M.A. &e. (Plate IX. A. figs. 1 & 2.)°.... 237
XXIV. On the Relationship of Ulodendron, Lindley and Hutton, to
Lepidodendron, Sternberg ; Bothrodendron, Lindley and Hutton; Siyil-
laria, Brongniart ; and Rhytidodendron, Boulay. By Rosrrr Kip-
STON, F.G.8.
COCCI, i Tt TT
XXV. Chilomonas paramecium. By SARA GWENDOLEN FouLkKn.
(Plate LX. B. figs. 1-6.)
XXVI. Report on the Testaceous Mollusca obtained during a
Dredging-excursion in the Gulf of Suez in the Months of February
and March 1869. By Roperr MacAnprEw.—Republished, with
Additions and Corrections, by ALFRED Hanps Cooke, M.A., Curator
in Zoology, Museum of Zoolozy and Comparative Anatomy, Cam-
bridge.— Part III. i
vi CONTENTS.
Page
XXVII. Descriptions of Sponges from the Neighbourhood of Port
Phillip Heads, South Australia. By H. J. Carrer, F.R.S. &..... 277
XXVIII. Remarks on a Paper by Prof. EK. D. Cope on the Rep-
tiles of the Province Rio Grande do Sul, Brazil. By G. A. Bow-
EEINGIEB pois 0 ey areiece soils, 6 nyore 9 aye le spayalermia ey oieve ee Oe 294
XXIX. Ona Collection of Lepidoptera made at Manipur and on the
Borders of Assam by Dr. George Watt. By Arruur G. Burier,
FLLS.,.F.Z:8., &e. (Plate VIL) 2 2.0.5. 3. . he 298
Proceedings of the Geological Society .............cee cess 310—312
On the Brisingide of the Expedition of the ‘Talisman,’ by M.
Edmond Perrier; On a new Species of Land-Tortoise, brought
by M. Humblot to the Museum of Natural History, by M. Léon
Vaillant; Orientation of the Embryo and Formation of the Co-
coon in Pertplaneta orientalis, by M. P. Hallez..... vee, JL2—815
NUMBER XCV.
XXX. Critical Observations on Prof. Leidy’s ‘‘ Freshwater Rhizo-
pods of North America,” and Classification of the Rhizopods in
general. By Surgeon-Major Watticu, M.D................... 317
XXXI. On a Collection of Lepidoptera made at Manipur and on
the Borders of Assam by Di. George Watt. By Arruour G.
owe EMS. EAS. y OCC. tal fe cialis eleiele i> «lode (chee 354
XXXII. Descriptions of Sponges from the Neighbourhood of Port
Phillip Heads, South Australia. By H. J. Carrer, F.R.S. &c..... 547
XXXII. On an Example of Polymorphism in the Amphipoda.
By Cuarues Curmton, M.A. (New Zealand). (Plate X.)........ 368
XXXIV. Notes on Australian Lepidoptera, with Descriptions of
new Species. By RupoLPH Rosenstock, B.A. (Plate XI.) .... 376
XXXV. Note on JLaceripora cribrosa, Hichwald. By RoBErtr
ErHeERipGs, Jun., and ArTHUR H. Foorp, F.G.S. .............. 385
XXXVI. Remarks on Mr. C. W. De Vis’s recent Contributions
to the Herpetology of Australia. By G. A, BouLENGER ........ 386
XXXVII. A List of Reptiles and Batrachians from the Island of
Nias.) By Ge AS BoumENGER 2.00.3 .e ec ewan ee. cece eee 388
New Books:—A History of British Birds. By Witi1amM YARRELL,
V.P.LS., F.Z.8. Fourth Edition, revised and enlarged : Vols.
I. & Il. by AtFRED Newron, M.A., F.R.S.; Vols, HI. & IV.
CONTENTS. ; Vil
Page
by Howarp Saunpers, F.LS., F.Z.S., &e.—Russian_ Central
Asia. By Henry Lanspext, D.D.—Our Insect Enemies. By
pre VOOD) . 2. 15. c.sueeycuerereitr feiss airy lets Sars 390—394
A Classification of the Sponges, by Prof. Sollas, D.Sc.; On the
Pelagic Annelides of the Bay of Algiers, by M. C. Viguier; On
the Organization of Truncatella, by M. A. Vayssiére ; On the
Development of Aurelia awvita and Cotylorhiza borbonica, by Dr.
A. Gotte; On the Original Fundamental Numbers of Medusee
and Echinoderms, by Wilhelm Haacke...............- 395—899
NUMBER XCVI.
XXXVIII. The Victorella pavida of Saville Kent. By E. C.
Bousriretp, L.R.C.P. Lond. (Plate XII. figs. 1-3.) ............ 401
XXXIX. Diagnoses of the new Species of Galatheidea collected
during the ‘Challenger’ Expedition. By J. R. Henprrson, M.B.,
F.LS.
XL. Notes on Australian Lepidoptera, with Descriptions of new
Species by RUDOLPH ROSENSTOCK, BtA. ...........0.00-:--> 421
XLI. Note on Ceratiwm hrundinella (O. F. Miller), its Variability
and Mode of Reproduction. By Dr. Henri Buanec. (Plate XII.
EBS, GBs) 0 © Obie AOE TO ECE ROIS nea Ire Cee eS en Pe arta an 444
XLII. Critical Observations on Prof. Leidy’s “ Freshwater Rhizo-
pods of North America,” and Classification of the Rhizopods in
general. By Surgeon-Major Watiicu, M.D. ........... patch 453
XLII. Descriptions of three new Species of Geckos. By G. A.
BE aNraURES NG TOLD reed Nor ac retouch cao ia y <yare) sien eke sote act BueBeee dp oS. dutiaashag 3a east 473
XLIV. Notice of two Lumbrici with bifid Hinder Ends. By Prof.
LE), g/SPTDTAAR ORV I BST Ops ER me Petr Pee ne at ee 475
XLV. Trachelius ovum. By SARA GWENDOLEN FOULKE ...... 477
XLVI. Description of the Marsupial Egg of Echidna hystrix. By
Epwarp P. Ramsay, Esq., F.L.8., C.M.Z.8. (Communicated by Sir
HapOse ne Ke Cs, BES OcCo) oct ada Siets « Maley wise seek osgeen cos « 479
XLVII. Notes from the St. Andrews Marine Laboratory (under
the Fishery Board for Scotland). By Prof. M‘Inrosu, M.D., LL.D.,
BEpoeroce.=—No- ITD; - (Plate XO) oe see. vec ery pene ea es yore 480
XLVIII. On the Nest and Development of Gastrosteus spinachia
at the St. Andrews Marine Laboratory. By Epwarp E. Prince.
MICROMINE) Sete Lane owt wisest ays azo Watered dps ois wenn 487
XLIX. On the Genus Fistulipora, M‘Coy, with Descriptions of
several Species. By H. ArtEyNE Nicuoxson, M.D., D.Sc., Regius
Professor of Natural History in the University of Aberdeen, and
Arruur H. Foorp, F.G.S., late of the Geological Survey of Canada.
(Plates XV .—X VIII.)
Vill CONTENTS.
Page
New Book :—Contributions to the Knowledge of the Older Meso-
zoic Flora of Virginia. By Wrortam Morris Fonratne.
Monographs of the United States Geological Survey. Vol. VI. 517
Instinet of Orientation in Helix aspersa, by F.d’A. Furtado ; On the
Existence of a Postoral Band of Ciiia in Gasteropod Veligers,
by J. Playfair M‘Murrich ; Results of a Faunistic Excursion
in the Iser-, Riesen-, and Glatzer Gebirge, by Dr. Otto Zacha-
rias; Note on the Blastodermic Vesicle of Mammals, by Prof.
A.C. Haddon, M.A.,M.R.I.A.; Noteon Halcampa chrysanthellum,
Peach, by Prot. Ay C3 Haddon, MvA. MR LAC). eeee 519—523
PLATES IN VOL. XVI.
Prats I.
mT:
“TI. Lepidodendron Veltheimianum.
nV):
Ve
evils
“NBUE,
“VIII. New Indian Lepidoptera.
“ TX. New Species of Araneidea.—Chilomonas parameecium.
X. Polymorphism in the Amphipoda.
- XI. New Australian Lepidoptera.
“XII. Victorella pavida—Reproduction of Ceratium hirundinella.
“XT. Ova of Callionymus lyra.—Staurocephalus Siberti—Stem of
Tubularia indivisa with Crustacean nests.
' XIV. Nest and Development of Gastrosteus spinachia.
Deep-sea and Shallow-water Hydrozoa.
Lepidodendron Veltheimianum and Species of Sigillaria.
New Species of Fistulipora.
FIFTH SERIES. oe No. 91.
| 51695 T HE an ey
MAGAZINE OF NATURAL HISTORY,
INCLUDING
ZOOLOGY, BOTANY, ann GEOLOGY.
No. XCTI.
JULY 1885,
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SO mon aunorcensaense per litora spargite muscum,
Naiades, et circtim vitreos considite fontes:
Pollice virgineo teneros hic carpite flores:
Floribus et pictum, dive, replete canistrum.
At vos, o Nymphe Craterides, ite sub undas ;
Ite, recurvato variata corallia trunco
Vellite muscosis e rupibus, et mihi conchas ;
Ferte, Dex pelagi, et pingui conchylia succo.”’
N. Parthenii Giannettasii Ec), 1.
No. 91. JULY 1885.
—s
I.—On some Deep-sea and Shallow-water Hydrozoa. By
JOHN J. QUELCH, B.Sc. (Lond.), Natural History Museum.
[Plates I. & II.]
THE forms described in the present paper consist chiefly of
deep-sea Hydroida which were obtained by Mr. C. A. Bishop
while engaged in repairing the cable off the Cape Verde
Islands. With the exception of the variety of Diphasta pinas-
ter, which was taken by Mr. Bishop from the Madeira cable off
Lisbon, and the specimens of Cryptolaria conferta presented
by Miss M‘Lea, the Hydroida were taken by Mr. Bishop
from the cable off 8. Antonio, the depth being, as Mr. Bishop
assured me, over 500 fathoms. Though but a very small
collection, yet the forms obtained are of great interest, since
they belong, with but one exception, either to new or rare
species, and throw considerable light on the classification of
their allied forms. As a contribution to our knowledge of
the Hydroida at great depths the collection is a valuable one,
while the many points which it serves to elucidate in the
characters of structures which had hitherto been imperfectly
known or altogether misunderstood give to it a special
interest. A definite contribution is thus made to our know-
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 1
2 Mr. J. J. Quelch on some
ledge of the gonosome of Streptocaulus, which throws consi-
derable light on corresponding parts in other genera; while
many facts in the variability of the corbula in Aglaophenia, in
the development of the ramuli in Streptocaulus and Antennu-
laria, and in the occurrence of nematophores in forms (Zygo-
phylax) other than the Plumulariide are clearly established.
The specimens were obtained under circumstances of great
personal inconvenience by Mr. Bishop as the cable came in,
and were carefully dried, preserved, and brought to the
British Museum, since, as he expressed to me, he thought it
likely that any specimens from the deep sea might be of
interest to naturalists. Mr. Bishop has thus earned the
thanks of all zoophytologists for this contribution which he
has made to their science, and has at the same time set an
example to all those who, whatever may be their station in
life, have more or less favourable chances of adding to our
stock of knowledge.
The specimens of Cryptolaria presented by Miss M‘Lea
are especially interesting, since they show the nature of the
gonotheca. Of much interest also are the specimens of Dst?-
chopora granulosa and D. conferta.
Order HY DROIDA.
Family Eudendriide.
Eudendrium annulatum.
Eudendrium annulatum, Norman, Ann. & Mag. Nat. Hist. 1864, p. 83,
pl. ix. figs. 1-3.
Two small specimens were obtained, which I have doubt-
fully referred to this rare species, with which they agree in
their shrubby habit, in their regularly annulated branches, and
in the irregular network of small tubes which cover the surface
of the main stems. It seems to differ, however, in that its
ramules are often much elongated, while the whole hydro-
phyton seems to be thinner and much more delicate throughout.
Family Lafoeide.
Lafoéa tenellula,
Lafoéa tenellula, Allman, Mem. of Mus. Comp. Zool. Cambridge, U.S.A.
vol. v. no. 2, p. 12, pl. viii. figs. 3 & 4.
Several specimens growing together on a portion of the
cable are referable to this species. The specimen on which
the species was founded evidently was quite a young one ;
for though the ultimate ramuli and the hydrothece are com-
Deep-sea and Shallow-water Hydrozoa. 3
paratively minute, yet the whole hydrophyton may attain with
age a comparatively large size, becoming erect or suberect and
branched, with the stem and chief branches fascicled. The
peduncle of the hydrotheca is very variable in thickness,
but it never becomes very thin; the rings of elongation of the
hydrotheca are generally very distinct and from two to four
in number. Height of the largest specimen about 80 millim.
when placed in water and allowed to disentangle itself from
the closely curled manner in which it dries.
Cryptolaria conferta. (Pl. I. fig. 1.)
Cryptolaria conferta, Allman, Mem. of Mus. Comp. Zool. Cambridge,
U.S.A. vol. v. no. 2, p. 17, pl. xii. figs. 6-10.
Specimens which do not seem to me to differ from this
species have been presented to the British Museum by Miss
M‘Lea. On some specimens, which I regard as female stocks,
occur curious large elongated bodies, which call to mind the
large elongated gonothece of various species of Campanu-
laria, and which leave no doubt in my mind that they are
the real gonothecz of the species. ‘These bodies are placed
on the branchlets and on the distal portion of the main
branches, and are directly continuous with one of the fascicled
tubes of the stem. They are about from four to six times the
length of the free portions of the hydrothece on the distal
parts, elongato-cylindrical with a plain circular orifice, con-
stricted at the base, where they join the tube of the stem, and
attached throughout their whole length to the branch or
branchlet from which they arise. They are often much
covered at different parts by small fascicled tubes of the stem.
Different structures have been described by Prof. Allman,
Mr. 8. F. Clarke, and Mr. J. W. Fewkes as occurring on
various species of Cryptolaria, which have been regarded by
them with more or less certainty as being the gonosomes of
those species. In the second part of the narrative of the
cruise of the ‘ Challenger,’ p. 752, in a note on the Hydroida,
Prof. Allman, however, states that on a specimen of this
genus, from a depth of 2600 fathoms, ‘we have been made
acquainted with its gonosome, which had not previously been
detected.”” As there have been so many different views as to
the structure of these parts, 1 have deemed it advisable to
notify the presence of gonothecz on this specimen, in order
that it may afford what confirmation may be possible to this
later view of Prof. Allman.
Loc. North Atlantic. Lat. 48°33’ 52", long. 10° 33/ 14”.
Brought up by the sounding-wire from a depth of 500 fathoms
(Mr, Hamilton).
18
4 Mr. J. J. Quelch on some
Family Zygophylacide.
Hydrothece continuous with, but not jointed to, a lateral
process of the stem; paired nematophores or nematophore-like
bodies at the base of the hydrothece, one nematophore being
on each side on the lateral process.
ZYGOPHYLAX, nov. gen.
Hydrocaulus erect, branched, composed of many tubes
ageregated together; branches unjointed ; hydrothece bise-
rial, alternate, tubular, sessile, narrowed and constricted to-
wards the base, and continuous with a slightly enlarged lateral
projection of the stem. On the raised lateral edges of this
process are placed two small, elongated, tubular structures,
one on each side at the base of the hydrothece, which are
constricted and jointed towards their base, and which do not
appear to differ in any essential particular from the jointed,
stalked nematophores which are characteristic of so many of
the Plumulariide.
Reproduction unknown.
This genus is only known in the dry state ; and the charac-
ters of its hydrophyton relate it, on the one hand, to the
Lafoéide, and on the other tothe Haleciide. It differs essen-
tially, however, from the forms included under those families,
and notably so in the possession of the paired nematophores
at the base of the hydrothecee—a character so striking and
constant as to justify, in my opinion, the formation of a new
family to receive it.
Prof. Allman, in his Report on the Plumulartide of the
‘Challenger’ expedition (p. 6), has given an extremely
valuable note on our knowledge of the occurrence of nemato-
phores or nematophore-like bodies in Hydroids other than the
Plumulariide, and it is interesting to note that such bodies
occur on forms allied or referable to Lafoéa and Halecium.
The present form adds another to the list with much the same
relation, though the certainty of its position in classification,
based on the details of the structure of the complete hydro-
soma, must await the confirmation derivable from fresh or
well-preserved specimens.
Zygophylax profunda, n. sp. (PI. I. fig. 4.)
Stem fascicled, erect, much branched; branches very thin,
springing immediately from beneath a hydrotheca, which
therefore becomes placed in the axil of the branch. Hydro-
thecee very small, alternately placed at regular intervals,
short, tubular, and curved so as to look outwards and down-
wards, with two or three annulations generally well deve-
Deep-sea and Shallow-water Hydrozoa. 5
loped near the margin, the base much constricted and
connected with a distinct but small process of the stem ;
aperture of the -hydrotheca circular. Nematophores extremely
small, elongated, being more than half the length of the
hydrotheca, slightly ringed near the margin, and jointed
below to a thicker basal portion which is placed on the proxi-
mal side of the base of the hydrotheca.
_ The specimens of this species form small branched colonies
which are about 30 or 40 millim. in height, and when dried
are of an earthy brown colour. They were found growing on
the cable and also attached to specimens of Diphasia pinaster.
In these dried specimens the delicate nematophores are often
found more or less broken away, but the remaining basal
portion easily marks their original position on each side of
the base of the hydrothece.
Family Sertulariide.
Diphasia pinaster.
Sertularia pinaster, Ellis & Solander, Zooph. p. 55, pl. vi. figs. 6 & B.
eens pinaster, Hincks, British Hydroid Zoophytes, p. 252, pl. 50.
g. 1.
Several specimens of this species were obtained. ‘They
agree in nearly every particular with the characteristic form
of the species, except that the female gonothece are usually
tetraspinous, bearing only the single lower circle of spines,
while occasionally on other gonothece on the same hydrophy-
ton two very small spines of the upper circle are also present.
In accordance with the position and prominence of the four
larger spines, the female gonothecee have when dried a more
or less quadrangular shape. ‘The spines on the female gono-
thecee of this species are thus seen to vary from four to eight.
The male gonothece are much smaller, and have the charac-
teristic quadrangular shape, with the four angles produced
into very prominent spines.
To this species I have referred, somewhat doubtfully, some
other specimens obtained from the Madeira cable off Lisbon,
in which the distinct fold at the point of divergence of the
superior half of the hydrotheca is scarcely or not at all repre-
sented. In other respects, in the characters of the hydrothece
and in the habit of the hydrophyton, they are closely like the
present species. They present a decided approach to the D.
coronifera and the D. elegans. No gonothece are present on
the specimens, and the final position of the form must remain
doubtful until the nature of these structuresis observed. For
the present I distinguish it as
Diphasia pinaster, var. arcuata.
6 Mr. J. J. Quelch on some
Family Plumulariide.
Several of the genera of this family are in great need of
revision. The characters by means of which Plumularia, for
instance, is separated from Antennularia are now become
extremely vague, since the verticillate arrangement of the
ramuli in the latter has had to be abandoned as a generic
character. In Antennularia the ramuli may be few or many,
verticillate or scattered, while in the young colonies and on
the basal parts of more advanced ones the ramuli are placed
singly and alternately, becoming afterwards placed in pairs,
a condition that obtains in the young forms of our common
Antennularia antennina. Plumularia does not thus seem to
have any constant natural character by which to separate it
from Antennulartia. The genera Antennopsis and Hippu-
rella seem also inseparable from Plumularta and Antennu-
laria. In speaking of Hippurella, I use the name as defined
by Prof. Allman in his “ Report on the Hydroids of the
Gulf-stream,’”’ where it is stated that the “ultimate ramuli
are alternate and pinnate towards the proximal ends of the
branches, but towards the distal ends surrounding the branches
on all sides, and here either scattered or regularly verticillate ;
each composed of alternate long and short internodes with
intervening groups of very short ring-like internodes, each of
the long internodes carrying a hydrotheca.”
Mr. J. W. Fewkes states (Bull. Mus. Comp. Zool. Cam-
bridge, U.S.A. vol. viii. p. 184) that in a form which he
has identified as Atppurella annulata, Allman, these verticil-
late branches are but verticillate ribs, destitute of hydrothece,
and that they bear simply a row of nematophores, being thus
a special form of the phylactocarp in which the gonophores
are borne between successive verticils of these ribs. Mr.
Fewkes has not stated, so far as I am aware, that this is a
redescription based on a reexamination of Allman’s type
specimen, so that, until such information be forthcoming, in
the face of the explicit statement of Prof. Allman quoted
above from his description, it seems unavoidable to conclude
that Mr. Fewkes has described some form which, though
closely agreeing in many of its features with the Hippurella
annulata, Allman, is quite distinct from it, and is truly refer-
able to a new genus.
Plumularia variabilis, n. sp. (Pl. II. fig. 2.)
Hydrocaulus attaining a height of more than 60 millims.,
simple, slender, not fascicled, very indistinetly jointed, and
Deep-sea and Shallow-water Hydrozoa. 7
springing from a tangled mass of small tubular filaments;
pinne alternate, distichous, extremely thin and slender, each
borne close to the distal end of an internode of the stem,
where it is supported by a long process much swollen at the
base ; the mode of jointing of the pinne is most variable, the
proximal internode is short and destitute of hydrotheca, and is
often followed by one or two short internodes before the hydro-
theca-bearing internode, so that there may be one, two, or
three distinct internodes between the process of the stem and
the first hydrotheca-bearing internode; the hydrotheca-bear-
ing internodes always long, frequently alternating with one
long non-hydrothecate internode, and not unfrequently with
two or three shorter ones, while, as frequently the internodes
which follow one another all bear a hydrotheca ; in this latter
case the internodes are extremely elongated, and instead of
bearing the hydrotheca towards the centre of their length,
bear them near their proximal extremity. Hydrothece very
small and shallow, their width and depth scarcely exceeding
the general diameter of the pinna. Nematophores extremely
numerous. Besides the pair placed at the sides of the hydro-
theca there is a single nematophore on the proximal part of
each hydrotheca-bearing internode, and in those cases in which
these internodes are much elongated and follow directly on
one another, two nematophores are placed at short distances
on their distal portion. On the long intervening internode
two nematophores are present, and when this is replaced by
two or more shorter ones, each then bears a single nemato-
phore. The proximal internodes which follow the process
bear a nematophore, and the internodes of the stem carry
ten or more; of these, two are carried on each side of the
internode in a line above the pinnez, so that there are four
nematophores between successive pinne on the same side of
the stem ; one is placed on each side of the proximal part of
the internode between the rows of alternate pinne, while two
pairs are placed on the process which carries the pinna, one
at its upper and one at its lower end.
The gonothece are short, suboval or slipper-shaped, and
slightly curved to one side, with an oval subterminal orifice,
borne singly or in pairs on the swollen base of the processes
of the stem in the axils of the pinnee.
In the dried specimens of this species a curious torsion of
the stem is observable, so that instead of there being two
straight rows of alternate pinne, a complete spiral is formed
by these rows in about a length of 30 millim. In this state
the arrangement of the pinne is singularly similar to what is
found in the genus Antennopsis, Allman, which, judging by
8 My. J. J. Quelch on some
the figures given, can hardly be separated from Plumularia,
since in all essential features the two genera seem to be iden-
tical, with but the slight exception that the single pinna
borne by each joint occasionally departs in Antennopsis from
the ordinary distichous alternate arrangement. ‘This condi-
tion seen in the dried state of the present species entirely
disappears when the specimen is placed in water ; the torsion
of the stem becomes lost and the specimen assumes the normal
pinnate habit.
In many of its characters this species recalls P. antennata
and P. megalocephala.
Plumularia delicatula, n. sp. (PI. I. fig. 3.)
Hydrocaulus attaining a height of more than 100 millim.,
simple, not fascicled, very distinctly jointed, of very variable
thickness in different specimens, and often quite slender,
rather wiry, arising from a mass of tubular filaments. Pinne
alternate, one on each internode, very thin and delicate,
attached to a rather short process of the stem, which is
scarcely or not at all swollen at the base; regularly jointed
with oblique joints; alternate internodes bearing hydrothece
and rather elongated, being nearly twice the length of the
intervening internodes, which are about four times as long as
they are broad ; each internode more or less marked by slight
annular constriction at their extremities, chiefly noticeable on
the proximal internode of the pinna. Hydrothece rather
deeper than their width, which is about twice the general
diameter of the internodes. Nematophores numerous, two at
the lateral margins of the hydrotheca and one at its proximal
side, one on the intervening internode, one or two on the
internode which is attached to the process of the stem; one
on each side of the base of this process, and two placed singly
along the stem on each internode in a line above the process
of the internode below.
Gonothecee borne in the axils of the pinne, flask-shaped,
elongated, with a short neck.
The delicate pinne in this species are often broken off in
dried specimens, when but a rather wiry stem is left. Its
closest ally seems to be Plumularia setacea, from which it
differs in the nature of the joints, in the relative length
and thickness of the imternodes, and in the disposition of
the nematophores on the stem and on its processes.
Antennularia trregularis, n. sp. (Pl. I. fig. 4.)
Hycrocaulus simple, jointed, slightly thickened, attaining a
Deep-sea and Shallow-water [ydiozoa. )
height of about 15-20 centim. or more, closely crowded to
form wide dense tufts, the hydrorhiza of which has the form
of a rather thin spreading mass of closely crowded entangled
filaments of different sizes. Ramuli extremely slender,
jointed, arranged in a very variable manner; on the basal
part of the hydrocaulus they are alternate, placed singly, one
to each joint, but in such a manner that they do not strictly
fall in the same plane; higher up the stem they are arranged
in pairs, the pairs decussating ; while in the larger number of
stems this condition is again lost at the upper part by the
ramuli becoming placed in threes at each whorl, each three
being so placed as to be vertically above or below every alter-
nate three, so that a hexastichous arrangement is produced ;
these upper ramuli are borne on a long process (of the stem),
which is slightly swollen at the base; one or two short inter-
nodes follow this process before the first hydrotheca-bearing
internode, while between the hydrotheca-bearing internodes one
long or two shorter internodes are placed. ‘The internodes
are very slender and usually much elongated. The hydro-
thece are small and shallow, slightly wider than the general
diameter of the ramulus. Nematophores rather variably
arranged ; one below each hydrotheca on the same internode
and two above it at the lateral margins, two on the intervening
long internode or one on each of the replacing shorter ones,
and one on each of the short proximal internodes following the
process of the stem; on this process one or two nematophores
are placed singly along the inner side, and one is placed on
each side of the swollen base, nearly in the axil of the ramulus ;
one nematophore is placed on the stem directly above the point
of origin of each ramulus.
Gonothecee borne singly in the axil of the ramuli, rather
short, suboval, and curved, with an oval subterminal orifice.
If the genus HMippurella as defined by Allman could be
maintained, this form would have to be referred to it; but it
seems to me impossible to retain that genus, since the varying
position of the ramuli on which it is founded is a common
characteristic of Antennularia, as shown by their earlier stages.
In the common British species, A. antennina, the ramuli are
at first arranged alternately, as in Plumularia, then in pairs,
before attaining their verticillate condition (Hincks, Brit.
Hydroid Zoophytes, vol. i. p. 281).
The species, in the general arrangement of its ramuli at
different parts of its hydrocaulus, recalls the species A. hexu-
sticha, A. Johnstoni, A. decussata, and A. Janini; but in
essential characters 1t cannot be confounded with either of
them.
10 Mr. J. J. Quelch on some
Aniennularia profunda, n. sp. (PI. II. fig. 5.)
Hydrocaulus fascicled at the base and springing from a
tangled mass of fine fibres, branched, erect, indistinctly or
rarely jointed below, more numerously so above, attaining a
height of more than 15 centim., and in the specimen obtained
remaining unbranched with subopposite pimnate ramuli for
nearly its whole height. At its upper end the ramuli lose their
pinnate arrangement and become irregularly placed, forming
four or six rows, two or three ramuli being often placed at the
same level and alternating with those above and below them,
but not closely crowded; where this subverticillate arrange-
ment of the ramuli takes place, young branches on which the
ramuli have the same subverticillate arrangement begin to
develop. Ramuli thin and long, attached to a long process
of the stem, which is swollen below, jointed, each internode
bearing a hydrotheca, and having a length between three and
four times its diameter. Hydrotheca small and shallow, its
width being about equal to the diameter of the internode.
Nematophores very numerous, four on each internode of the
ramulus, one at its distal and one at its proximal part, and
two at the lateral margins of the hydrotheca, two pairs on
each of the lateral processes of the stems in the proximal
portions of the colony, and three pairs on those in the upper
portions, two on the proximal and three on the distal parts of
the stem above the point of insertion of each ramulus, while
lines of nematophores are found running up the stem between
the rows of the ramuli. In the axil of each ramulus is a
slight swelling with a small pore, apparently a base for the
attachment of gonothecez. Gonothece unknown.
This species is close to A. ramosa, from which it differs
chiefly in its general habit, in the arrangement of the ramuli,
in the relative length and thickness of the internodes of
the stem and ramuli, and in the disposition of the nemato-
phores on the stem. It differs markedly in essential charac-
ters from A. tetrasticha, which it much resembles in general
habit. It is close to A. norwegica, but is easily distin-
guished by its branched hydrocaulus, its more verticillate
ramuli, by the relatively short and thick smooth internodes,
and the number and disposition of the nematophores
throughout.
Aglaophenia acacia.
Aglaophenia acacia, Allman, Challenger’ Hydroida, pt.i. p. 38, pl. xii.
figs. 1-4.
Numerous specimens were obtained which differ in unim-
Deep-sea and Shallow-water Hydrozoa. 11
portant points from the ‘ Challenger’ type specimens. They
consist of simple unbranched stems, the larger of which are
about 70 millim. in height, and they are thus destitute of the
characteristic habit which marks the old specimens of the
species. ‘The type specimen figured in the report on the
‘Challenger’ Plumulariide was full-grown and evidently an
old specimen, while the present specimens are but young
forms. With the exception of this difference of habit, due to
age, and of a slight difference in the corbula, the forms agree
in every essential respect. The difference in the corbule
presents itself in their variable length. Sometimes the cor-
bula is composed of a few pairs of leaflets, especially in those
at the distal parts of the colony, where there are usually
about six or seven pairs, while again there may be present a
large number of pairs, ten or more, which are chiefly placed
on the proximal parts. The shape of the corbula conse-
quently varies considerably, from a rounded oval to a narrow
cylindrical form, the one passing insensibly into the other.
Tn essential characters this species seems to be extremely
close to A. tubulifera, A. calamus, and A. rigida.
Streptocaulus pulcherrimus. (Pl. I. fig. 5.)
Streptocaulus pulcherrimus, Allman, ‘Challenger’ Hydroida, pt. i.
p: 48, pl. xvi. figs. 1-3,
Of this beautiful and extremely interesting form five
colonies were obtained, one of which attains a height of about
30 centim. They are especially interesting since they supply
the characters of the gonosome which were wanting in the
‘Challenger’ specimens, while at the same time the origin of
the spiral arrangement of the hydrocladia from the pinnate
form is clearly seen at the proximal parts of the colonies. In
some of the colonies the hydrocladia are absent from the basal
part for a distance of about 5-8 centim., while in others they
are continued nearly to the extreme base. These basal
hydrocladia are confined to one side of the stem and are
alternately arranged on each side of a line of more or less
rounded adnate nematophores, and spread in opposite direc-
tions, thus having a strictly pinnate disposition. Above this
basal part the planes of the hydrocladia gradually become
closer, until the hydrocladia become placed in one and the
same plane intermediate between their former positions, and
are attached not on each side, but in the direct line of the
nematophores of the stem. The torsion of the stem now
gives the spiral arrangement which is so distinctive of this
form. In the dried state this spiral arrangement is scarcely
12 Mr. J. J. Quelch on some
or not at all perceptible; but on placing the specimen in
water it assumes its normal habit.
The gonosome consists of gonothece, which are borne
neither directly by the hydrocladia nor by modified protective
branches, but are seated directly on jointed appendages of
the hydrocladia, one gonotheca to each joint. ‘These appen-
dages are placed laterally at the upper basal part of the mesial
nematophore, immediately below the base of the hydrotheca,
and are always situated on the left side—left, that is, to one
standing in the hydrotheca, so to speak, and looking towards
its pointed margin. ‘They are unbranched and jointed, and
are placed either on consecutive mesial nematophores or
irregularly. The joints are similar throughout, generally
three or four in number to each appendage, narrowed at the
base and expanded at the top, so as to be obconical or sub-
triangular ; the expanded upper lateral edges chiefly formed
by two rather short nematophores, one at each edge, between
which is placed the narrow base of the joint above, while
below this point of juncture and on the front of the joint (that.
is on that part which looks towards the hydrotheca below
which the appendage is situated) is seated the gonotheca,
which thus occupies the upper anterior portion of the joint.
The remaining anterior portion of the joint is evenly divided
by two transverse constrictions.
The gonothece are sessile and elongato-pyriform, with a
suboval subterminal orifice; they are placed one on each
joint of the appendage, and, where broken away, leave their
base of attachment exposed to view.
From the structure of the parts thus described it will be
seen that the genus Streptocaulus calls to mind the peculiar
condition found in Cladocarpus, in which the ramuli bearing
gonothecee are not strictly modified hydrocladia, but appen-
dages of the hydrocladia, with this essential distinction,
however, as it seems to me, that while in Cladocarpus these
structures may possibly be imagined as being more or less
protective, and thus as peculiar forms of the phylactocarp
according to the definition of Prof. Allman, yet in Strepto-
caulus they can in no sense be considered as protective, but
seem rather to be a repetition on a more complete scale of the
structures found in such a genus as Schizotricha.
In Schizotricha the gonothece are not strictly borne by the
hydrocladia, but on a basal portion which seems strictly
homologous with the reproductive ramuli of Cladocarpus. A
multiplication of such parts as the basal segments of Schzzo-
tricha, giving a jointed ramulus, in which each joint bears
Deep-sea and Shallow-water Hydrozoa. 13
lateral nematophores and a gonotheca, is the exact condition
found in Streptocaulus; while in Cladocarpus this condition
is carried a step further, in that the ramuli become branched,
with few or many joints, some of which only bear gonothece.
Schizotricha has been referred by Prof. Allman to the
section Gymnocarpa of the Eleutheroplea, and Cladocarpus
to the section Phylactocarpa of the Statoplea; and, judging
on the point of function as to whether the reproductive appen-
dages of the hydrocladia on which the gonothece are placed
are or are not protective, the genus Stéreptocaulus must be
removed from the Phylactocarpal Statoplea, among which it
was temporarily placed, to the section Gymnocarpa. On the
other hand, since the reproductive appendages and segments
which bear the gonothecx seem in the three cases to be strictly
homologous, and thus but rudimentary or varying forms of
the phylactocarp, it seems necessary, if the terms Gymnocarpa
and Phylactocarpa are to be retained with any definite
meaning, that all three genera should be placed among the
phylactocarpal forms.
Order HY DROCORALLINE &.
Family Stylasteride.
In the following descriptions of new species of the genus
Distichopora detailed mention is made of the characters of the
surface of the ccenosteum, of the form and mode of arrange-
ment of the pore-rows, of the relative size, shape, and position -
of the gastropores and dactylopores, and of the nature of the
ampulle. Short descriptions, with special reference to these
characters, are also given of those previously-described species
which agree with them more or less closely in general form
and coloration, in order to point out the more marked differ-
ences which are presented by those species. The characters
of the ampullee call for special notice in the diagnosis of the
species, since well-marked differences in the structure of these
parts obtain in different species of the genus. Such certainly
may be aftirmed after a very careful examination of a large
number of stocks in which the ampullee present the appearance
of raised more or less vesicular swellings on the ccenosteum.
For the figures given of the cyclosystems parts have been
selected at some distance from the extreme apical points,
since at such points the dactylopores become markedly tubular
and prominent in all or nearly all species of Distichopora.
14 Mr. J. J. Quelch on some
Distichopora granulosa, n. sp. (Pl. I. fig. 1.)
Coenosteum branched, regularly flabelliform, somewhat
incrusting at base, of a rich scarlet-red colour on the distal
portion of the main branches and throughout the branchlets
even to the tips, except where fracture has taken place at the
extremities, the small commencing growth at such points
being very pale reddish; on the basal part of the main
branches and on the incrusting portion the colour becomes of
a pink-red. Branches short and thick for the size of colony,
being about 7-12 millim. thick at the base of branches that
are about 30 millim. in length, and diminishing gradually in
size to about 2 millim. diameter at the tips, compressed at the
base, round above; branchlets short, round, obtuse, rather
thickened at the base and about 2 millim. thick at the apex,
which is often slightly expanded where division is taking
place. Coenenchyma dense, the surface conspicuously
roughened and granulated either by crowded bluntly conical
eminences, between which are placed small scattered pores, or
by sinuous irregularly confluent or reticulated ridges, which
are more usually found towards the distal parts of the
coenosteum.
Cyclosystems regularly arranged on opposite sides in
distinct, deep, continuous lateral furrows, the width between
the outer edges of the dactylopores being about °75 millim.
Gastropores rather small, circular or slightly elongated trans-
versely, slightly unequal and unequally separated, the partition
between them often equal to their diameter, and not rising
above the bottom of the furrow; style deep, very thin, and
obsoletely hirsute ; in section the gastro-canal is seen to be
nearly smooth. Dactylopores large in comparison with the
gastropores, being about one third to one fifth the size of the
larger gastropores, placed on the margin of the furrow, at
distances apart generally exceeding their width, elongated
transversely, with their outer and lateral margins much
elevated above the surrounding surface, so as to present in
profile a series of distinct tubular or spout-shaped eminences ;
the inner margin is generally wanting, so that the dactylopores
open on that side into the gastropore furrow. Ampulle
abundant, scattered irregularly or closely grouped, forming
rounded eminences about 75 millim. in diameter, marked on
the upper surface by the small sinuous irregular ridges which
are characteristic of the coenosteum, between which are several
small scattered irregular pored openings, which communicate
with a single cavity within; the walls of the ampulle become
very thin with age, and finally break away.
Deep-sea and Shallow-water Hydrozoa. 15
Locality. Raratonga?’ B.M.
Two specimens of this handsome species were presented to
the national collection by Prof. Flower.
A marked feature of this species is the strikingly rich
coloration, which is continued even to the tips of the coenos-
teum, except where fresh growth, consequent on fracture,
has commenced. This character, with the special structure of
its coenenchyma and of its cyclosystems, will readily serve
to distinguish it from all other species. Special. attention
must be called to the decided resemblance which obtains
between the forms of the dactylopores in this species and in
those of the genus Errina.
Distichopora conferta, nu. sp. (PI. I. fig. 3.)
Coenosteum forming an intricately and crowdedly branched
fastigiate clump, in which the branchlets on the separate
branches are arranged in a more or less flabellate manner ;
of a delicate carmine-red colour, with whitish tips. Branches
much divided, short, very slender and round, slightly com-
pressed at the extreme base, and very seldom coalescent ;
branchlets very small, round, obtuse, about 1°5 millim. thick
at the apex, which is slightly expanded where division is
taking place. Ccoenenchyma dense, the surface strongly
granulated, marked throughout by small, crowded, conical
eminences, between which are minute scattered pores.
Cyclosystems regularly arranged on opposite sides in conti-
nuous rows, seldom forming furrows, except at the extreme
apical points, since the partitions between the gastropores
are usually level with the general surface. Gastropores
rather large, seldom circular, more often slightly elongated in
the direction of the rows, usually with a very irregular
outline and rather prominent septa-like internal projections,
as though in process of division, unequal and unequally
separated, except at the apical parts, where the partitions are
very narrow; style very deeply placed, thin and finely
hirsute ; in section the gastro-canal is found to be papillose.
Dactylopores quite minute, irregular, unequally placed,
elongated slightly in a transverse direction, nearly even with
the surface, except at the extremities, where they are rather
elevated and tubular. Ampulle (apparently female) abun-
dant, scattered or grouped, forming rounded eminences nearly
1 millim. in diameter, marked by straight radial ridges,
generally from 5 to 8, which pass from the centre of the
ampulla to the outer border, where a circle of rather large
16 Mr. J. J. Quelch on some
pored openings, closed by thin membranous tissue and placed
between the ridges, leads into the single central cavity of the
ampulla.
- Locality. Raratonga. B.M.
Two specimens of this beautiful form were presented
to the national collection by Prof. Flower. I have been
enabled to describe this species through the courtesy of
Prof. Charles Stewart, who first remarked its specific di-
stinctness.
A very fine specimen in the museum of the Royal College
of Surgeons agrees most closely, except in the characters of
its ampulle, with this species. ‘These ampulle are raised
and confluent, the individual ampulla being undistinguishable
in the mass. Their surface is covered by the conical
markings characteristic of the coenosteum, and is irregularly
and rather sparsely pored with minute openings. This form
of the ampulle is constant throughout the stock, while that
described for the species is constant on the two stocks in the
British Museum. I am strongly inclined to think that these
confluent ampullate swellings are the forms characteristic of
the later stages of the ampulle of the male stocks, which in
the earlier stages are sunk beneath the surface of the ccenos-
teum. This seems to me borne out by the fact that ina
large series of specimens of D. violacea in the national col-
lection the two forms of the ampulle are present—the one with
the stelliform much swollen eminences, which, though grouped
together, are distinct from each other, and are bounded by an
outer circle of pored openings; the other with smaller
swellings, in which separate ampulle are seldom distinguish-
able, and having scattered minute pores over the surface.
This species, though close to D. granulosa, differs from
it in many particulars, of which the crowded corymbed mode
of growth, the coloration, the smaller and more slender habit,
the nature of the surface, the arrangement of its cyclosystems,
and the size, position, and form of its dactylopores and
gastropores may be cited.
Distichopora Miles, Quelch.
D. Milesti may be separated from both of the foregoing
species by its very slender regularly flabellate coenosteum ; by
the minutely granulated or smooth surface, which is rendered
rough and uneven only by the wregular and abundantly
developed ampulle ; by its dull lake-red or almost crimson
colour; by the very distinct, wide, deep, continuous lateral
Deep-sea and Shallow-water Hydrozoa. 17
furrows, about 1 millim. in diameter from the extreme outer
edges of the dactylopores; by the very large gastropores
slightly elongated in the direction of the furrow; by the very
small dactylopores which are placed on the distinctly raised
ridge of the furrow but above which the separate dactylo-
pores are but slightly prominent except at the apical parts ;
by the papillose gastro-canal ; and by the smooth outer surface
of the massed ampullz which are neither roughened by ridges
nor lined by regularly-arranged pored openings.
Distichopora coccinea, Gray.
D. coccinea may be distinguished by its flabellate coenos-
teum with much compressed branches and branchlets, crowded
on their faces with numerous short often tuberculate young
branchlets, which at first are perpendicular to the general
plane of the ccenosteum; by its dull crimson-red colour ;
by its smooth surface; by the small and shallow but
distinct lateral furrow; by the small gastropores which lead
into a smooth canal and are separated by rather wide parti-
tions; by the very minute dactylopores which are not raised
above the general surface and which are separated by distances
generally greater than their own diameter; and by the di-
stinctly raised ampulle which are smooth on their upper
surface and are surrounded at their base by a circle of com-
paratively large pored openings which lead to the central
cavity and which are separated by septiform partitions passing
to neighbouring ampulle or to the surrounding ccenenchyma.
Distichopora rosea, Kent.
D. rosea is distinguished by its irregularly flabellate coenos-
teum with rounded, thick, obtuse branches and branchlets ;
by its smooth surface which becomes slightly granulated
with obtuse conical eminences towards the apical parts; by
its deep peach-blossom red colour ; by its extremely wide, deep,
distinct lateral furrows which are interrupted at the angle of
branching ; by its comparatively small unequal gastropores,
unequally and often widely separated; by the obsoletely
papillose gastro-canal; by the extremely large dactylopores
(easily distinguishable by the naked eye), the imner margin
tailing, so that the pore opens into the furrow while the outer
and lateral margins are much elevated and thickened; and by
the ampulle, which are undistinguishably massed together in
large raised groups with minute pored openings scattered
over the irregularly granulated upper surface.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 2
18 Mr. J. J. Quelch on some
Distichopora brevisertalis, Quelch.
D. brevisertalis is distinguished by its irregularly flabellate
coenosteum, with short, thick, obtuse branches and branchlets,
the branches being much compressed at the base, rounded
above, and often coalescent; by its pale aurora-red or deep
flesh-red colour; by its granulated surface, the small conical
granules being much enlarged and more prominent at the
distal parts; by the obliteration of the pore-rows, except at
the apical parts of the branches and branchlets and at the
parts of the ccenosteum where fresh branchlets originate ; by
the rather small unequal gastropores, which are placed in an
irregular line at the bottom of a shallow furrow at the apical
parts, and which gradually diminish and disappear by over-
growth; by the nearly smooth gastro-canal; by the small
dactylopores, which are placed on the edges of the shallow
furrow at the extremities, but which become gradually even
with the surface, and finally are obliterated; and by the
ampullee, which are often grouped together, and consist of a
raised central portion which is marked on its upper surface
with small, more or less radial, rather sharp ridges, and is
surrounded by a circle of comparatively large pored openings,
which are separated by thick septiform partitions with which
the ridges are continuous, passing to neighbouring ampulle
or to the surrounding ccenenchyma; in the later stages of
these ampulle, when the central portions break away, the
group presents the appearance of a rough mass with irregular
pores, in which the single central cavities of the ampulle are
hardly distinguishable from the surrounding openings which
lead to them.
Distichopora gracilis, Dana.
D. gracilis is distinguished by its regularly flabellate and
extremely slender habit ; by its fainter or reddish coloration ;
and by its compressed branches ; but a more complete descrip-
tion of the type specimen of this little-known species is re-
quired, since little or nothing is known as to the nature of its
coenenchyma, its surface, its cyclosystems, and its ampullee.
Distichopora nitida, Verrill.
D. nitida is distinguished by its large regularly flabelliform
habit; by its rounded branches, somewhat compressed at the
base ; by its rounded obtuse branchlets, expanded at the tips
during division ; by its extremely variable coloration, ranging
Deep-sea and Shallow-water Hydrozoa. 19
from bright red to light orange; by its minutely granular
surface, becoming almost smooth at the basal parts; by its
obsolete or very shallow lateral furrows, the partitions between
the gastropores being generally raised to the surrounding
surface; by the unequal large gastropores; by the minute
superficial dactylopores ; and by the scattered or grouped raised
granulated ampulle, in which the pores communicating with
the central cavity are arranged in a circle around the base,
the septiform partitions between them passing off to the sur-
rounding coenenchyma or to neighbouring ampulle.
Distichopora ochracea, n. sp. (FI. I. fig. 2.)
Coenosteum branching in a plane, of a dull ochre-yellow
colour, sometimes becoming white at the tips; branches
thick, rounded, or slightly flattened; branchlets short and
rather thick, rounded, obtuse, expanded at the tips before
division takes place. Coenenchyma rather firm; surface
minutely granular at the basal parts of the branchlets,
becoming more granulated at the extremities, with crowded,
very obtusely conical eminences, between which are scattered
pores. Cyclosystems regularly arranged in continuous, wide,
shallow lateral furrows. Gastropores irregularly placed,
unequal, but generally very large, circular or elongated trans-
versely, separated by very narrow partitions, which are often
raised to the general surface; gastro-canal very crowdedly
papillose; style very deeply placed, slender, and finely hirsute.
Dactylopores very unequal, some rather large, others very
minute, elongated transversely, the outer and lateral margins
scarcely or not at all raised, except at the extremities of the
branchlets, where the inner margin is continuous with the
rounded edge of the furrow, along which the dactylopores are
closely placed. Ampulle scattered or grouped, consisting of
rounded eminences with slightly developed subradial ridges
on the central portion, surrounded at the base by a circle of
pored openings which communicate with the single central
cavity and which are separated by septiform partitions passing
off to neighbouring ampulle or to the surrounding ccenen-
chyma.
Locality. Solomon Islands, 14 fath. B.M.
This species is founded on a small piece of a coenosteum
which was dredged by H. B. Guppy, Hsq., M.B., R.N., Sur-
geon to H.M.S. ‘ Lark,’ and by him presented to the national
collection. It is very distinct from all known species of the
genus, being most closely related to the D. nitida, Verrill.
DQ
20 Dr. R. v. Lendenfeld on Australian Sponges.
EXPLANATION OF THE PLATES.
Puate I.
Fig. 1. Distichopora granulosa, natural size, showing ampullee.
Fig. 1a. Ditto: pore-rows, magnified.
Fig. 16. Ditto: dactylopores, with ridges of the surface, seen laterally,
magnified.
Fig. 1c. Ditto: ampulla, magnified.
Fig. 2. Distichopora ochracea, natural size, showing ampullee.
Fig. 2a. Ditto: pore-rows, magnified.
Fig. 2b. Ditto: ampulla, magnified.
Fig.2c. Ditto: gastro-canal in section, magnified.
Fig. 3. Distichopora conferta, natural size, showing ampullee.
Fig. 8a. Ditto: pore-rows and part of surface, magnified.
Fig. 3b. Ditto: ampulla, magnified.
Fig. 4. Zygophylax profunda: portion of hydrophyton, natural size.
Fig. 4a. Ditto: branch, magnified.
Fig. 46. Ditto: hydrotheca and nematophore of one side, magnified.
Fig. 4c. Ditto: part of fascicled stem, magnified.
Fig. 5. Streptocaulus pulcherrimus : proximal part of stem, magnified.
Fig. 5a. Ditto: reproductive appendage with gonothecz, magnified,
Fig. 5b. Ditto: gonotheca, magnified.
Prats II.
Fig.1. Cryptolaria conferta: part of stem with gonotheca, magnified.
Fig. 2. Plumularia variabilis: part of stem with pinna and gonotheca,
magnified. ;
Fig. 2a. Ditto: part of another pinna, magnified.
1g. 8. Plumularia delicatula: portion of stem with gonotheca and pinne,
magnified.
Fig. 4. eae wrregularis: stem, showing arrangement of
ramuli.
Fig.4a. Ditto: part of stem with ramuli, magnified.
Fig. 4b. Ditto: gonotheca, magnified.
Fig. 5. Antennularia profunda: stem, showing arrangement of
branches and ramuli.
Fig. 5a. Ditto: portion of stem, proximal part, magnified.
Fig. 5b. Ditto: portion of stem, distal part, magnified.
Fig. 5c. Ditto: portion of ramulus, magnified.
II.—WNotes to the Australian Sponges recently described by
Carter*, By Dr. R. v. LENDENFELD, in Sydney.
As I am just now engaged in writing a Monograph of the
Australian Sponges I was particularly glad to receive the
* H. J. Carter, “ Description of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia,” Ann. & Mag. Nat. Hist. ser. 5,
vol. xv. p. 196.
Dr. R. v. Lendenfeld on Australian Sponges. 21
publications on the subject by Carter, through the courtesy
of the author.
There are, in the part concerning the Ceraospongie and
Myxospongie, no figures, and the diagnoses are so short that
it is, in by far the greater number of species, impossible for
me to identify them with those in my collection, or to ascer-
tain those characteristics which I consider as the most im-
portant.
There are a few, however, which, in consequence of some
accessory peculiarity or other, I have been able to recognize.
My collection of several thousand specimens of Australian
Sponges is by far the finest as yet brought together from any
one locality, and I think that not only Carter, but also all
other scientists who are working at the Sponges, will be
interested in the result of a comparison between Carter’s
diagnoses and the specimens in my collection.
Halisarca australiensis* is not a sponge at all, but the
crusts described by Carter under the above name are the ova
of Boltenias surrounded by their folliculi. 1 myself believed
that the slimy coatings in question were perhaps sponges,
and I examined them accordingly. ‘The results of this exami-
nation are laid down in a paper published by me last yearf.
The Boltenia is probably Boltenia australis. The name
Boltenia australiensis given by Carter{ is not warranted.
Chondrilla uncula, O. §., is mentioned as occurring in
Port Phillip§. I have not found any, specimens of this
sponge on any part of the Australian coast. I have, however,
described a species of Chondrilla as C. secunda, n. sp., from
Port Phillip, m a paper read some time ago before the Lin-
nean Society of N.S. W.||, which is somewhat different
from CO. uncula, O. S., in the shape of its spicules and parti-
cularly the configuration of the canal-system, but which out-
wardly appears very similar to the Adriatic species, of which
I brought aspecimen with me. I thinkit very probable that
Carter’s specimen is to be referred to my Chondrilla secunda,
a sponge very abundant in Port Phillip.
* H. J. Carter, ‘‘ Description of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia,” Ann. & Mag. Nat. Hist. ser. 5,
vol. xv. p. 197. ; ; ; ak
+ R. v. Lendenfeld, “ On the Slimy Coatings of certain Boltenias in
Port Jackson,” Proc. Linn. Soc. N.S. W. vol. ix. p. 498.
{ H. J. Carter, /. c. p. 197.
§ H. J. Carter, J. c. p. 200.
R. v. Lendenfeld, ‘“‘ A Monograph of the Australian Sponges,” Ab-
stracts of Proc. Linn. Soe. for January 1885,
22 Dr. R. v. Lendenfeld on Australian Sponges.
Luffaria digitata* is very meagrely described, but I think
it highly probable that it is identical with a sponge described
eighteen years ago by Selenkat as Spongilia cactos, and
which has been investigated by F. E. Schulze} and myself§.
Carter has, apparently, not seen my paper on Sponges of
Port Phillip, otherwise I think that my description of this
sponge would have been sufticient for identification. I have
named it Dendrilla rosea, which name, having priority, ought
to replace the name Luffaria digitata given by Carter ||. The
most important feature of the sponge is its peculiar subdermal
cavity. Carter does not mention this; but as he does not say
anything about the canal-system at all, it is probable that he
never examined any section-series.
Darwinella australiensis{ is represented in my collection,
but the canal-system is not described by Carter, so that it is
difficult to identify the species.
With Aplysina levis** of Carter, seven distinct species in
my collection might be identified. These are very different
from one another, but all coincide with Carter’s diagnosis of
the above species. They are forms which lead to the Dysideidze
of Marshall}, of which Carter’s Pseudoceratina durissima tt}
may be a true representative.
The diagnosis given by Carter of Aplysina purpurea§§ led
me to believe that it might be identical with a sponge exa-
mined by me and named Aplysilla violacea||||; but now it
* H. J. Carter, “Description of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia,’ Ann. & Mag. Nat. Hist. ser. 5,
vol. xv. p. 201.
+ E. Selenka, “ Ueber neue Schwimme aus der Stid-See,” Zeitschrift
fiir wissenschaftliche Zoologie, Band xvii. Seite 566, Tafel xxxy. fig. 5.
t F. E. Schulze, “ Untersuchungen tiber den Bau und die Entwicke-
lung der Spongien,” Zeitschrift fiir wissenschaftliche Zoologie, Band
xxx. Seite 379.
§ R. v. Lendenfeld, “ Ueber Ccelenteraten der Sud-See.—II. Neue
Aplysinide,” Zeitschrift fiir wissenschaftliche Zoologie, Band xxxviii.
Seite 271 ff.
|| H. J. Carter, 7. ¢. p. 201.
q H. J. Carter, 7. c. p. 208.
** H, J. Carter, /. c. p. 204.
++ William Marshall, ‘‘Ueber Dysididen und Phoriospongien,” Zeit-
schrift fiir wissenschaftliche Zoologie, Band xxxv. Seite 92.
ty H. J. Carter, 7. ¢. p. 204.
§§ H. J. Carter, “ Contributions to our Knowledge of the Spongida.—
Order II, Ceratina,” Ann, & Mag. Nat. Hist. ser, 5, vol. vil. pp. 103-
105.
\||| R. v. Lendenfeld, 7. c. Seite 257 ff.
Dr. R. v. Lendenfeld on Australian Sponges. 23
seems that this is not the case, as Carter considers the Austra-
lian specimen of that sponge to be identical with his Pseudo-
ceratina durissima *.
Carter's new genus Holopsamma T is identical with Mar-
shall’s genus Psammopemma }, established five years ago,
and the latter name must be accepted accordingly as having
priority.
The species described as H. crassa§ and A. levis || cannot
be distinguished. I possess in my collection numerous tran-
sition forms between them, and all these ought to be com-
bined under the name given to them previously by Marshall{,
viz. Psammopemma densum. I think, however, that I shall
be able to distinguish a few species, as the canal-system is’
not the same in all the specimens I have examined. It is,
however, a matter of quite unusual difficulty to make good
series of sections through these arenaceous sponges.
Holopsamma laminefavosa** may be identical with Mar-
shall’s genus Psammodema Tf.
Both Holopsamma fuliginosatt and H. turbo §§ are unrecog-
nizable.
The establishment of a new genus Sarcocornea |||| for a dry
Dysidea is not justified. In the diagnosis there is nothing
by which the only species could be distinguished. from
Dysidea.
Dysidea fragilis, Johnston {], and Dysidea Kirkit, Bower-
bank***, are mentioned. I only possess the latter in my col-
lection. Chaliniform species are very abundant, and I
possess long series of continuous transition-forms. [ ee
this shape to be a mimicry of the true Chalinide, which,
consequence of their axial spicules, would not be very diss
tible food.
I cannot say anything about the species described as
Dysidea hircineformist tt and chaliniformis ttf. The descrip-
*H. J. Carter, “ Description of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia,” Ann. & Mag. Nat. Hist. ser. 5,
vol. xv. p. 200.
abt Ie Garter, tec. alll:
¢ William Marshall, ‘“‘ Ueber Dysididen und Phoriospongien,” Zeit-
schrift fiir wissenschaftliche Zoologie, Band xxxv. Seite 113.
Sp Hy). Canter, @. cp. 211" ll Hi. J. Carter, 7. c. p. 212.
Il
44) H. J. Carter, Zc. p. 215. 3
ti H. J. Carter, f. c. p 217. foto ete
q W. Marshall, Zc. Seite 113. * H. J. Carter, J. ¢. p. 212.
++ W. Marshall, 7. c. Seite 109. tt H. J. Carter, 7. c. p. 213.
§§ H. J. Carter, /. ¢. p, 213. ||| H. J.C Carter, i.e. p. 214.
tcael Dae |p Carter, lc. p. 216.
J.
Carter, l. ¢. von ALI
24 Dr. R. v. Lendenfeld on Australian Sponges.
tions are so short that it is simply impossible to make any
use of them.
I consider the genus Dystdea as characterized by the
following points :-—
1. Transparent hyolin. Mesoderm without foreign
bodies in the ground-substance.
2. The canal-system and ciliated chambers of Spongelia
as described by Schulze *.
3. Foreign bodies forming all the fibres.
It cannot of course be decided by the description whether
Carter’s specimens belong to the genus Dysidea in this sense
or not.
The sponge deseribed by Carter as Spongelia stellidermatat
is probably identical with some specimens in my collection,
which, however, do not belong to the genus Spungelia, but
to another familyt, that of the Spongide. I have named
this sponge Cacospongia gracilis §; but it may appear neces-
sary to establish a new genus for it. At all events it does
not belong to the genus Spongelia, Schulze, who was the first
to establish a diagnosis on a really reliable and scientific
basis ||.
Carteriospongia caliciformis{] is described from a dry speci-
men, so that no opinion can be hazarded on its real position
in the system.
As the configuration of the canal-system is not described
and the microscopic structure of the soft parts generally hardly
referred to, and as these are considered all important by me,
it is only natural that I should not be able to utilize Carter’s
essay. Justas it was necessary that O. Schmidt should com-
* F. E. Schulze, “Untersuchungen uber den Bau und die Entwick-
lung der Spongien: Die Gattung Spongelia,” Zeitschrift fiir wissen-
schaftliche Zoologie, Band xxxii. Seite 117 ff.
+ H. J. Carter, “Description of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia,” Ann. & Mag. Nat. Hist. ser. 5,
vol. xv. p. 219.
t J. Vosmaer, “ Studies on Sponges.—I.” Mittheilungen der zoologi-
schen Station in Neapel, Band iv. Seite 445. Vosmaevr’s classification is
identical with mine, which I arrived at independently, and which is
therefore very likely to be correct.
§ In 1883 I identified the sponges from several museums, and I sup-
lied several with names, the diagnoses of which remained in schedule,
The sponges referred to can be seen in the museum of the South Aus-
tralian Institute at Adelaide.
|| F. E. Schulze, /. ¢.
4, H. J. Carter, 7. ¢. p. 221.
On the Teredo utriculus of Gmelin. 25
pare Bowerbank’s species with his own, I find it advantageous
to review Carter’s essay from my point of view, so that in the
future any one may be enabled to make use of it.
For any one who holds views similar to those of Polejaeft,
Vosmaer, and myself, this review will be most welcome, as I,
in possession of extensive collections and working the subject
on the spot, am best able to judge.
I11.—On the Teredo utriculus of Gmelin, with Remarks
upon other Ship-worms, By Sytvanus Hanzey, F.L.S.
Ke.
Untiu lately this ancient species, founded upon a well-exe-
euted drawing in Kammerer (Conch. Cab. Rudolst. t. i.), was
omitted, or neglected, in our lists of sea-shells. Of late it
has been cited as asynonym of the 7. norvagicus of Spengler,
a conclusion which my recent exanunation of a most magni-
ficent group acquired by me at Cannes from the wreck of a
submerged Italian ship does not confirm. It may, indeed,
be a variety, yet with differences in tube, valves, and pallets
so perceptible that the untrained eye (I mean as to shells)
of a portrait-painter immediately indicated them. I may
remark that the Histulana corniformis of Lamarck (as picto-
rially defined by a reference to Favanne) seems identical ;
the tube, at least, is closed at the broader end by a dome-
shaped covering (as in the genus Septaria, =Kuphus), which
with the bar-like stricture at the narrower extremity are the
principal features exhibited in Kiammerer’s plate. The
pallets are more leaf-like and with shorter stalks than in nor-
vagicus, the tube (besides its dome, which some say is
present, although I have not myself found it) in all adult
members of the genus is more fragile, and the thin valves
easily distinguishable by their outline, the fang or central
portion being broader and much shorter in proportion than
in the solid dark-skinned northern shell to which it has been
affiliated. The most striking character, however, is the large
space occupied by the finely sculptured triangular area, which
descends far down the broad fang.
The species (or variety, if you will) is a southern form ;
but I obtained many young specimens (valves only) from
Guernsey, an outlying province of the Mediterranean fauna,
26 Mr. Sylvanus Hanley on the
which I cannot distinguish. The more prominent features
seem the peculiar thinness of the valves, whose swollen
triangular area is so large as to occupy one half the entire
length (hence the fang seems peculiarly short).
During the last twenty years four principal monographic
lists of the Teredines have been published by Jeffreys, Fischer,
Tryon, and Sowerby. The last, the only one which has been
illustrated, and consequently the only one which will enable
the mass of collectors to determine their specimens, is by
Sowerby in his hurried conclusion of Reeve’s ‘ Conchologia
Iconica.’ Unfortunately he has neglected the many new
species (subericola, excavata, bipartita, spatha*, fusticulus)
described by Mr. Jeffreys in the ‘ Annals and Magazine of
Natural History’ for 1860; these, although elaborately de-
scribed, are unknown to me (for want of figures or, perhaps,
of examples), as well as to most conchologists ; hence illus-
trations of them would have been generally acceptable.
As my long study of this genus and the possession of a
remarkably fine collection of Teredines have enabled me to
correct certain errors in the ‘ Iconica,’ and to suggest addi-
tional statements, I venture to critically annotate many of the
species indicated. In order to obtain absolute certainty as to
what the draftsman actually intended, I have carefully looked
for the examples declared to have been drawn from specimens
in the British Museum, where, although aided by the Curator,
I have often failed to discover them.
The sequence here followed is that adopted in the text
which accompanies the four and only plates.
T. navalis.—The reference to Sellius, who expressly men-
tions that he uses the term ‘‘ Teredo marina’”’ { generically,
should be pl. ii. figs. 2, 3,6; to Spengler, Skriv. Nat. Selskab.
vol. i. pt: 1, p. 103, pl. ii. fig. C.
T. norvagica.—The reference to Spengler’s monograph
should be pl. ii. figs. 4, 5, 6; to Z. nigra, Blainville, Diction.
Sc. Nat. vol. li. p. 267, as in ‘Quarterly Review,’ pl. 1.
fig. 20,a,b. TZ. naviwm of Sellius had better have been
omitted, for although that author classed all the ship-worms
known to him as Zeredomarina (a compound generic name),
he has copied (?) a bud-shaped pallet, which he regarded as
* Pallets in British Museum, ¢este Jeffreys.
+ Teredo means a borer; the adjective marina is used to distinguish the
salt-water worm from Zeredo vestiwm, the larva of the clothes moth.
Hence it is logically absurd to claim precedence for it.
Species of Teredo. 27
the T. navium of Vallisnieri; judging from the figure that
pallet has a shorter stalk and is more tapering at the broader
end than is customary in this species.
T. bipennata.—This is not the shell delineated in Turton’s
‘Conchological Dictionary’ (figs. 28, 40). The valves look
like those of the erroneous navalis of Spengler (Skriv. Nat.
Selskab. vol. ii. pt. 1, pl. u.), the pallets of which (perhaps
they are worn) seem unlike any of those figured in the
“Tconica,’ and remind one of the original drawing of the lost
palmulata. The two pallets delineated in the ‘ Iconica’
surely belong to two different species, the short-stalked one
possibly to Gray’s carinata. 1 could not find them in the
British Museum, as stated in the text. Mr. Edgar Smith
assures me that he can find no shell there under this name
which agrees with fig. 3, a, or any two dissimilar pallets like
those represented by fig. 3, 0.
T. Stutchburii.— The truncated pallet seems broken, yet is
not so really. As Blainville (Dict. Sci. Nat. vol. xxxii:
p- 268) professedly described this shell from a manuscript
species of Leach’s, which formed part of our national collec-
tion, it may reasonably be supposed that the identification is
correct ; yet Blainville asserts that the pallet tapers* rapidly
from the first joint to the last, which is not the case in the
specimen marked as Leach’s type, nor in the figure supposed
to represent it.
T. carinata.—This shell was no manuscript species as sup-
posed. The name was published by Gray as that of a new
species, and by Blainville, as of Leach’s manuscript, almost
contemporaneously. Gray’s monograph appeared in Taylor’s
‘ Philosophical Magazine’ for December 1827 (p. 411, copied
in Hanley’s ‘ Recent Bivalves,’ p. 4); the volume (lii.) of
the ‘ Dictionnaire des Sciences Naturelles’ bears date 1828 ;
both authors described from an example in the British Museum,
presumably the same as that roughly delineated by Sowerby,
who unfortunately represents for it the Teredo previously
published (1819) by Turton as 7. bipennata (Conch. Diction.
p- 184, figs. 38, 39, 40). But Gray indicates that the base
(or stalk) of the pinnately articulated pallet is short, whereas
it is represented by both Turton and Sowerby as decidedly
long ; evidently, then, the carinata of Sowerby is not that of
* The drawing is scarcely to be termed a likeness.
28 Mr. Sylvanus Hanley on the
Gray, who subsequently referred the forgotten 7. pennatifera
of Blainville (doc. cit. p. 269) to Turton’s species. The
British Museum does not possess the beautiful pallet ascribed
to it in the text of the ‘ Iconica.’
*T. megathorax, Gould.—In what work? Can the name
be a mistake or a misprint for 7. thoracites of Gould’s ‘ Otia’
(from Proc. Bost. vol. vi.), otherwise omitted? It is cer-
tainly, however, not the Calobates thoracites of Wright in the
Linnean Soc. Trans. (vol. xxv. pl. Ixiv.), or its ally C. aus-
tralis (ib. figs. 1-5), both of which are here omitted.
T. campanulata, Deshayes.—This supposed manuscript
species has been quoted by Tryon—whose monograph evinces
a most painstaking research—as the real Stutchburyi of Blain-
ville! I could not descry the delineated valves in the British
Museum ; but Mr. E. Smith writes as follows :—‘ The figures
give a very rough notion of the valves copied. ‘The auricle
is both too long and too wide, and in fig. 9, a, the anterior
area is not sufficiently large.”’
{Z. Saulit.—This supposed manuscript species of Professor
Wright combines the valves of the Nausitora Saulii of
Wright (Trans. Linn. Soe. vol. xxv. pl. lxv. figs. 9-15) with
the pallets of Kuphus Mannii of the same plate (figs. 1-8).
Such combinations render identification hopeless to those
whose libraries and whose leisure for research are limited.
T. batava.—This is not the shell designed by Spengler
(Skriv. Nat. Selskab. vol. 11. pt. 1), whose characteristic figure
of a pallet (pl. 11. fig. 8) coincides precisely with that of the
navalis of the ‘ Iconica,’ and is very different from the one here
depicted. Surely the ascribed locality Batavia (which is not
* «Two specimens had been so labelled in the British Museum from the
Cumingian collection. The drawings differ in several particulars; the
lower or narrow end of the valves (fig. 8, &) is much too incurved, and
the inferior margin of the anterior area is also too arcuated. In fig. 8, a,
the auricle is too prominent, and the central portion of the valve too
narrow.” —K. SMITH.
+ Mr. Smith writes that, although the drawings are rough and incor-
rect, yet they are perhaps better than those in the ‘ Linnean Transactions.’
Fig. 10, a, seems to him imaginative, for he could not find anything like
it in the museum. The tablet indicated Callao, not Callas Bay; the
specimens came from Miss Saul (1853), and why Professor Wright
ascribed them to Port Phillip, Australia, was unknown to him.
Species of Teredo. 29
appended to the example delineated) is not an imaginary one,
derived from the supposed specific name Batava (Dutch).
_ From a recent publication one learns that the European
species still devastates the dykes of Holland.
The valves of the false batava are not so unlike those of
utriculus ; the pallets, however, differ from any I possess.
T. afinis and T. brevis, from “ Mus. Deshayes”’ (his
collection has been purchased intact by the French govern-
ment for, I think, the Ecole des Mines; it is not in the
zoological gallery of the Jardin des Plantes), should be rather
“copied from Deshayes’s published figure;” probably
Deshayes did not possess the shell. It is a frequent error in
the ‘Iconica’ to ascribe to authors the possession of species
which they have only borrowed. In some of the earlier
volumes indeed the metaphorically stereotyped “ Mus. Cu-
ming ’’ was attached to shells lent by myself *.
T. palmulata.—Lamarck so inadequately described this
shell from its pallets alone that various members of the
section Aylotrya have been adjudged its representative.
Nevertheless the pictorial definition is fair enough. Adan-
son in 1759 (Mém. Acad. Paris, pl. ix.) figured three ship-
worms as the ‘I’aret de l'Europe, T'aret de Sénégal, and Taret
de Pondicherri (figs. 11,12). From this last almost every
figure of 7. palmulata has been more or less ill copied. I do
not find anything like it in the ‘ Iconica,’ and certainly not
the one here figured, which is probably the one so named by
Thomson as an Ivish species; [ also, in youthful confidence,
had accepted (Brit. Moll.) the same determination. Mr.
Jeffreys, who accepted as typical some pallets in the Parisian
Museum, from which he says “ Lamarck described the
species,’ though that author neither referred (as usual) to the
museum nor to his own cabinet for the source of his descrip-
tion, asserts that they somewhat approximate but are distinct
from those of bipennatus, and thus, indeed, they appear in the
original engraving, which displays more than a score of
articulations that taper from the first joint to the (brushy ?)
apex; the stalk only occupies one third of the entire length.
These specimens once belonged to Réaumur, and agree with
* As the fate of typical or even figured examples is not unimportant, I
may state that very many of those rightly ascribed to “ Mus. Metcalfe”
and ‘Mus. Reeve” have passed into the collection of the author, who
also purchased all the types described by Benson from Frederic Layard’s
cabinet.
30 Mr. Sylvanus Hanley on the
the characters of Gray’s ideal of 7. palmulata (from a speci-
men in the British Museum). Blainville, who avowedly
derived his description from Adanson’s plate, has ascribed to .
his 7. Stutchburyi* pallets which precisely suit those of
Adanson’s figure, but says the valves are perceptibly less long
than broad, which does not agree with the more equal height
and breadth of the valve portrayed in Adanson’s memoir.
It is possible that the valves and pallet in one case or the
other did not belong to the same species. It might save some
confusion, if the shell be really a recognizable one, to prefer
the earlier Lamarckian appellation of bépalmulata (Syst.) T.
In the synonymy of the Sowerbyan palmulata appears the
name 7. Philippii, Fischer. This name was first applied by
Gray (Ann. & Mag. Nat. Hist. 1851) to Philippi’s erroneous
ideal of Z. navalis (En. Mol. Sic. vol. i. pl. 1.); but no
description was attached to his correction.
T. minima, also annexed as a synonym, was very briefly
described, in French only, by Blainville, in his often-men-
tioned monograph, as having a very long stalk to its pallet.
T. senegalensis.—Blainville, who has given this name to
the Taret du Sénégal of Adanson (Mém. Acad. Paris, 1759,
pl. ix., and Voy. Sénégal, p. 263, pl. xix.), observes that the
pallet is truncated, not “ bicornée.” As these words did not
harmonize with the pronged pallet depicted in the ‘ Iconica,’
I was puzzled, but found on examination of the museum
types that the fault lay in the drawing, which, as Mr. E.
Smith declares, gives “but the feeblest notion of the pro-
cesses copied.”” Adanson’s figures, indeed, are so roughly
executed that I hardly dare conjecture what they were de-
signed for (navalis?, &c.). None of them, however, resemble
the equally indefinite species of the ‘ Iconica.’ The difference
of outline in the valves of Adanson’s three species 1s not very
marked.
T. nucivora.—As the illustrator has stated that he had not
seen the pallet, it is a pity that he did not more precisely state
* Mr. Edgar Smith observes that “the only shells in the museum
labelled 7. palmulata were pencilled by Mr. Samuel Stutchbury (a
dealer) as coming from Sumatra.” He could not find either valves or
pallets which would suit the figures in the ‘ Iconica,’
+ IT ama little reminded of Adanson’s figures by the valve and first
joint of the pallet of 7. (Xyl.) Dunlop of Wright (Trans. Linn. Soc.
vol, xxiv.), a shell mentioned in Sowerby’s monograph.
Species of Teredo. 31
the source from which he copied it (fig. 17, c); the delineated
specimen * differs a little from the earlier representations of
it, being shorter than in Spengler’s drawing (Skriv. Nat.
Selsk. vol. ii. pt. 1, pl. ii. fig. D). The statement that the
British Museum had furnished the specimens is an error.
T. denticulata.—The reference should have been to Gray
in Ann. & Mag. Nat. Hist. 1851, p. 386, where this name is
given, without appended description, to the undescribed and
supposed erroneous navalis of Méller. Naturalists might
have been congratulated that this undeterminable shell was at
length defined, only unfortunately the jagged tooth-like pro-
jection on the side of one of the pallets of the museum speci-
men (received from Mdller, I fancy) seems the result of an
injury or malformation. Both sides of the pallet are repre-
sented as symmetrically jagged, but this was imaginative.
My. Edgar Smith remarks that the valves are inaccurately
drawn.
In making these comments upon the monograph of a pecu-
liarly difficult genus, I wish expressly to declare that my
criticism is solely designed to prevent the perpetuation, or
origination, of errors which would spring from a misplaced
confidence in the existence of specimens in the national col-
lection.
It is the only illustrated monograph of the genus, the
materials for which are too scattered and too rare to be
readily accumulated and compared. An abundance of speci-
mens and a fine library are absolutely indispensable to a
conscientious naturalist, and even to obtain access to the
latter is almost impossible for a scientific conchologist who
permanently lives in England. Rich shell-collectors buy
costly specimens, yet for names sponge upon the brains of
those whose books they refuse to purchase.
* “Mus. Brit. and Sow.” “No tube, valves, or pallet like these
drawings are in the museum.”—EpGar SmirH,
i a a a ISA A
‘sourddipiyg ‘aopéesg fosrey ‘Sutar ‘aemtoeds oug |*'**
Mr. A. H. Cooke on Testaceous Mollusca
32
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3.odarg—* UNIT
3d
obtained in the Gulf of Suez.
Ajssopyoor (ey, *d ‘1A “qouog ‘uey) wodzy,
‘QATPOUTIS
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. xVi.
Ann. & Mag. N. Hist. Ser. 5. Vol
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ay} IVY} 9q 07 savedde aonjora puw ory
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‘GIST “ISTH “JEN “SU 3 “UTy) qyTUIg
‘DIDAGIZAIY SE TALS “sn ‘Quq oq} Ut 7 ae c Syn +) URIS
sotoeds @ 0} Ajjoexe puodseatoo syjoys ey, |-10,7] “92 ‘soutddrpyg ‘vous mon | pues “WIR OZ-OT ‘elRI ION | °° spuagzy “BaoRTOTA .
‘soutddytyg | ‘sy eque “W123 g ‘erer yoN | 2aaaar “eVepneotAcsq STINT,
Mr. A. H. Cooke on Testaceous Mollusca
*sMOYS
‘SN “ING oy} ur sodA, oy} 4ev sours
eB sv ourystp AyTeyNTOSGe ST 4T YOrTA WOT
‘spurpy ‘vqnunuah yim sotoeds oy} soqran
*syIVUIOY, “MOIgNGIIISIqy “MOT}EIG an TPAS
34
obtained in the Gulf of Suez.
ESE
jo syremjg {sueuttoeds mog | Yq “ear ——
“41 Suyqttos
-op Woy urerjer [ ‘omnyeur st suetutoeds
elt} ey} Jo euou se ynq ‘Mou ATquqoad
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EE fo EAMETS)
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‘sotoeds MoM & OJUT opeUt Suto 5
ptoae 0} tvou ApUeTOYINS ore sTToYys ey
“Sn “JMG OY} UI purywaowea Jo SuUdTIIOEdS [ ‘wosyoue
ay} WIA Tworyuepr Apoynjosqe you yonoyTY |Hog ‘eiperysny ‘meoutA "39 JT | [‘suouttoeds soryy, || ‘Lasso“g “eurzueouta | ——
; EE AE
‘sourddrpyg |" ype} ¢-G {uemttoeds omg) |**** aaaayy ‘soptosstt
[‘oyto ‘sy equ “qyey
eq ‘Q “s[ s,poomummmg| ‘oytord |¢-G ‘Sunok ‘uemtoeds ouy semog ‘msurmng vypouqdeg,
‘pmprany Jo says
Sono oq 0} yno sun} Joy} 944 ,,+ POUTUT
-1ajepun setoeds 0M4,, 9} JO 9UO ST SILT, SEEN ciee Mean? RAs ‘suotutoeds xg |*"** *[ypueugy “eared |] ——
‘soutddrmg | “st eqn “ype G-z foreyy | * * * aaaagr “enpta
‘spurpy ‘2727 jo wAuouAsS
B LaqyV] oY} SULIepIsuod UI WITY MOTTO; yOu
-uv0 [ ynq {adver ‘nsow.0f= se ‘arco
‘ngmjassag SuIpIVsat UL Jpstr stm9es OAL, ‘Lanaagr “esoumt0y =
‘TTaYs yueteyrp vB oqimb st ‘spurpy ‘vpopjassa7, | [sourddyrgg] ‘twssvovyy jo sweyng} ‘sy Teque “mayest Gg ‘ater jadaaay |spurzy “ey eT[OS80}
‘GPL d ‘q1gT “wsey, ‘00g “Aor
‘01g UL wosmayp DY? B Pedtiosop sey
SpoOAA-UosIuay, toy ‘pocueyo oq pnoys
euvu oy} ‘moyAuY “s1vnynuato TIA [BOTy
“uept st “CJ/ST “ISTH, “JeN “SBI 2 UAW)
yg “wuoswaype Ayureyt90 { soroeds jo
IUIIOBIP plVa B 99N71}SMOD UBD TOIT O14ST
-rojovrvyo Aue yuosord you op (ed49 8,X8t4)
‘Iq, Wor peteu ATqvumnserd) ‘sn “yg
ey} ut suetutoeds eyg, ‘AurMuouds oy}
0} poppe oq ysnum ‘pornsy roaou ynq “gg *d
B%
©
. ‘
Mr. A. H. Cooke on Testaceous Mollusca
36
‘gag ‘d “atx “Feel “ISLET YON ‘ORIN Fy ‘UL
UL poeqiosep sv soroeds jnjyneeq siqy,
‘sorjdde
osje vsounibgns “ifagq atepuh yarewmer
oy} Por 07 ,“pourmzejepun ‘seroeds oun ,,
OY} MOAf OLB SULMOT[OT OA4 OY} puUB STILT,
7DI4IQL JO SMITH
-roads Sunok ATuo ore Loy} : Urece oUOL AA
‘oAaoy ‘sunbhaja ppe
samiofisnf jo KurCuouds oy} OJ, your}srp
ayn st wpnorwing Sorcary ‘suudofrsnf 440q
Axe sT[eys oy { UOLVOyTUEpIsIM reyZoUW
*aA001T
pus ‘py ‘n7ng72a212 vey, pus ‘edcery
‘syonib ete Yor Jo dort} ‘suevtoods
XIs suIyjuoo pred oy} S'uoryy ‘a0072.19
0} puodsert09 pomBn sn} ST[OYS oy} JO ouONy
[‘sopfayo£og)]
‘somrdd yy
‘sourdd rit
‘860 URIPUT
bot beobeeerrdeoeee
sourddryiy
( Wosyoer sr 310g |
"eee “d “AIX “PRST ISTH JEN “OVI FY UAV
“4ST] STU} Ut sotoeds Surpoo
-o1d GJIM poytUepr oureq woIZ WMeyy jo
uoy10d sqetepisuod v szuoAeId ssozyqnop
qorga ‘aoripuoe peq ut puv oynutm ArToA
O1¥ ST[OYS oy} JO AuvUL {sty} MOTOq LET STLVE
seloeds peytjueprun jo requnu oy} AqtTeat
uy ,/peurmazeyapun soroeds x1s-Aqu0M) ,,
94} WOT a1v soloeds SUIMOTI[OJ OY} pue SILT,
bebo 660 bob @ o d'o db
‘ST 8, pooyy paory |f suottoeds
aL nn i IS RE elt | per
*SsyTCULO IT
Se
HOHNG ISIC
[‘suountoeds omy, ] \[yz2eugy ‘tesnoyi0ye 4A | ——
[‘suempoeds omy | |[ yzeeugy ‘wunrepjoyohos | ——
[‘suoutoeds exom omy] |'** * ‘Laaaaay ‘stiova]] ——
‘[anaagr © pp “eyeyqLA
‘suotutoeds oAty |-113] aaaayy ‘voovytideo
‘Laaaaay ‘stut10y
‘suouroeds omy, |-1snj] aaazay “ejnotiang ——
‘Lao § PY
‘eqeqyIALIy § aaaaaz ‘SI{IO
‘adRl JON [HeLa | wary “voorqia, vavyy hCG
[‘stevntoods omy ||**** [spuezy “toands] ——
[ ‘sueunioeds ae ‘Laaaaay ‘stpeproverdd | ——
[‘suewroeds x1g]|*****- [aaaaay ‘sand | ——
[‘suompeds omy ||** [yzeugy ‘euvousozy | ——
‘IVI JON |'uwy7T ‘soploqmoyL BipLoueyy
[‘suompoeds qycry | |* *[sobuzy ‘eq earpimue, | ——
[‘uourtoeds og || ‘[ypeewg “esowercqns |] ——
‘TeqNE JO 87Ve14C EDS
[oay] omy, |‘sisuotsoudjod viouvajeq
ores TAS
“Ul UG SBA 19}}2] OM} OT} JO JOYJNe OTT,
‘pay ‘seusofwhd pues “os ‘eng pus
seroeds sty} maeMjoq wolouystp oytocds
prea Aue vos 07 Aq1ptqeur Aux sseymoo ysnut T
“punsinogy 04 surfb
epjpa st pumbunung yeux (Tg ‘d ‘epet
'S'Z ‘q) SesseyW0o JfosuIy ZnpoOoIy ‘asTAd
~1940 10 yeInyns ‘spavq Surfattoue eyed 0x3
Ul suolyeIIVA oy} UO ATULeUT 4s0r 07 rwodde
Wey} UseMjeq seouetayip pasoddns oy,
‘Cuey) arog ‘vfne pure ‘(q2) ‘jaar, ‘oune
simog ‘(SPST 'S 'Z ‘d) ‘P9el ‘vumbunung
soloeds 014, 94} Usemyoq uorjeredos
O oul] e}IUyep dus MeIp 07 o[GQvUN We J].
37
‘sourdd ria
[ uoqinog] ‘seutddiyiyg
[‘uoqinog | ‘sy eTjayaheq
[-vmeueg ‘uepyezepy ‘10 X odeg “sy
yormpurg] ‘ow opweg “sy Areurg
‘wanjnoredo Auo4ys & (stqy tory
“MoU OU Seop suVpY) culAvy ‘worgnAT OnTy
BSt][oys oy, ‘exet} poradoostp eq ATqeq
-o1d [TM 47 ‘WeeURAIOJIpe|, OY} JIqey
“UL JOU Soop vz2vLOWWDU “\ueseId 4% MOTH
OM SU Ivy os ‘osnvdeq ‘ouo eqeyTeULoL
AIOA BST UONVOYUEpl oy, ‘Wnosnur sty}
UL MOU OLB v7MLOUW.UL Jo sadky OY} OsNBD
-eq e0Uepyu0d e10UK OY} YIM UOT}LOSSU
sry} oye y pur ‘(71g “d ‘GST ‘S'Z ‘dd
UL poqiiosep) pyp.1ouwwU ssuEpy ‘TT Y4LMA
ST[eys zong ey) Jo AyyWapt oynjposqe oy} 07
88 Uot}senb ou oq wed ory} uorutdo Aur uy
obtained in the Gulf of Suez.
(ar) ‘sy Aveaeg
“BIJ VIS
somiddyryg |sexy ‘prep ‘oroys ‘ayeropoyy |***
“poulutoyr yy,
‘wny “eyoreuE ——
*pouttoyr fT ‘Tuo ‘emnr="7oag7 |
sey “peop ‘eroys {ore janaay ‘euetourmng = ——
“pommmoyr yy
sey ‘peep ‘eroys {omy | '**** ‘wawayy “eararts
‘pomumoyey Sexy
‘peop ‘oxoys ‘uomtutos yoy |* “ww “euojsouBeut
‘pus
“Tey G 07 oL0ys “yuonberg |" * “way ‘euroo0LeDt ——
1a
-Uspl outeq sotoods oT}
suoysonh yoIoy, ‘pues
“ayer g-G ‘suepy “Hepa |’ PY ‘7 “eyeroutteut ——
*poulmoy
-By, SUyy ‘eLOYyS fare gon |**?* aaaagy ‘snyjase vorye Ny
"HT CIOILVN
pene NE TET TTP SN gg ST
“TUTYR I, "yyey g-g ‘yuonbeay |**** “pp ‘p ‘snzeotas ——
‘pomen ATYSIt st pxvo SIT, ie ete One bee} be hr Os ‘ vop py ‘snqptsnd ——
‘smppisnd 4OU st 41 yng “no ex 07
(IOM 00} SI 1oy}0 oy S "py “Vy ‘s77n07)nq
aq oj savedde oug ‘seroeds yourystp oy ‘lpr ‘Ky ‘snzveqyeq |
04 Sursuojeq ‘suetatoeds omy ATUO ore otoULT, ‘soutddtyiqg ‘oreyy | ‘pp “Pv ‘snqpisud snostpeq¢) |
"IMO[OI-o801
1481] B Jo puw ysorz A109 ore suotmioeds oxy, ‘sourdd yy ‘TBE OSV-ZL fore | 'pP Pp “eyeynqns |
‘sourdd pia. ‘IRE pf eawel gon | > cpp py ‘stperqrot |
[‘s] Yormpurg] ‘snywmey| ‘“qyey PF {exer AToyexopopy |'*°* ‘wo “eyesn1109 —— |
i a
['uedep] ‘sourdditqg ‘pues “TB OS-ZI ‘orey |" ‘stplowts = eyjeprmersg |
‘H AITIAAINVUA
THOME CAME
‘uojfog, [*purysy poopy pxory]|‘eroys uo yuenbeazun yon ‘[ jooay “eqnor |
‘om ‘any, ‘yUIOg 107,
‘uotunery |‘eroys uo yuonborjun oN |" ‘pp ‘Py ‘eyRonr or0yrae A
[‘Brtmop “prop
"TOT}OOT[ON OY} UL JON |-eTR@Q MeN ‘uoqinog]| ‘seurddrpryg \‘eroys uo ‘suewtoeds eaLqg|''** “7 “efnpea stsdoqztzay
“HW GISTOLINH NY
‘oleqy | PP ‘A “eqnuiw, viaeypewery
‘UIfeTLD Jo vyednd pura
OKT UOIULOD oY} st Torys ‘setoeds stqy “peuuroy ‘[ yay “ered |
fo Surjoqe] oy} Ul evISTUI otMOS ST CLOT], [soutdd iia ‘reqenbuery, | |-eqq sey ‘peop ‘eros ‘ orery |*poagy “euelyoreuey BorzEN, |
‘YovUIV'T JO vynunut
qqeuva yevyMeutos ATqeqord exozoreyy :
pus peynqiysrp-Ajoprm oy} YA pezun |
aq [JOM Avux Loy, puv ‘(Toys yseT oT3
WO SYIVUIAL oY} des) LoyvUt-soroeds 07v.10]0A
‘SHAVUOT MOH NALISIC TONRIg TeUS
Mr. A. H. Cooke on Testaceous Mollusca
38
ececrctnets eect | a a | |
a ee
‘SUMMpULY UMO S,MOIPUVOVP UI 4ST] [LULSIL0 oy} 0} poppe ore poyfeqey snqy SOT}I[CoOT pure setoedg ,
omes 047 st “(GIT d “2981 ‘SZ ‘d) “SUV
‘DpywU DILWOQIN GE *a}B4S Sed} SIL UL [TES
ay} JO «nopoo snasnf-ofns oy} Jo suremoed
yy Ajdunis ere peqttosep exeyy sazuaosafne
apyjod wpsnhun aospf out, “[T9R8T “ISUET
JON ‘SVL WY UnWy Woy sunep vynwsvf
+9 “(Ist “d ‘gest ‘8 °Z ‘d) Aqmtoud oavy
[TIA omen 10},R, eT], “vosnf mrzzruuayQ
se suepy “vy Aq poqtiosep [joys cues ony
39
jo o7e48 poyovetq pue peep oy} ATdunis st 41 ‘pry “eosnt=] py
R |sB ‘roqje8oqye aveddesrp ysnux soroeds sry, Leyeasny ‘g ‘urdep] ‘euryg ‘ole |p “eqeroseziq §—B[[TUOqang,
S ‘ds ‘u ‘uoutoeds ony) |** per “pF ‘eamqta emesy
. 'BG1-961 “dd ‘OZ8T “ISIE “JEN “SPT
> juny ut ‘coded sty} ut surepy “w jo sotoeds
SS, [Atom doqjo 079 [Te YIM toyJ0S0} ‘poqrmoseq| °° °° pineal Des iS ‘Su ‘uouttoeds oug| ‘pp ‘py ‘enomSatd vutac
& "PV “V ‘2 7/aj0W20 YIM poyTyUEpT oq ‘Ler “PF “eyqeqzout0 |
> [OF SE PUR “vuaynqns Wo. JoULSIP SI [Toys ONLY, [peg vorog] -‘ueder ‘uoumtoeds ouQ) | ‘pp 7 “eurfnqns ——
ns ‘ueder ‘stoumtoeds OMT, | *** ‘pp 7 “eurdnd ——-
= ‘ds ‘u ‘uoumtoeds eu |-**- ++ ‘pp “Fy “epron, ——
“S JN Huerws0g, ‘aeder pue sourddyiyg ‘orey [°° pp Fe ‘eyeTNoIow ——
3 | ‘sourddyyry g ‘suotmpoeds oomgT | * +" pp y “st[re —
-= ‘ueder ‘oley | “pP ‘p ‘eyeyornd vjoursa
iS 7 [pry ‘snyvay
ES "PV “V ‘snzveq0q eq 04 savodde qjoys OTL [ovueputyy | ‘ueder ‘memtoeds ou¢, -[eq] ‘oP ‘Pp ‘sneqqtA
‘jNU}SeTO pur UM Jo
Seysep Ino[Oo “prum}y T[V 7B 4OU [LOTAd 4SeT
‘PI[OS e1our Youur ore sTeys esoyy {syop Jo
S}[9q Iv[N.dot oNsTIe}OvIeYO oy Jo usIs Aue
sMoys eno ATUO sueuttoeds mee}zy 40qe Jo Py
MOQ ‘“sngnpyassag jo Ajowea poyrvur ATOA W ‘OYBQSVIN JO ‘ST "UIRT G-G S erVl yon |p] ‘2npy ‘snyeyjesse7 ——
‘soroeds yuereytp ev oyimb Jo usuitoeds
Smmod v8 st [Toys YAXIs og, ‘Avs youuro T
“py ‘saproyaga.oz Jo urduouds v st ‘t001g,
FO JOU “Touery Jo sepavwh “Ag oyy St Yor
‘jessy “esawarye soroads oq} LayzET AA. PW “YAR ‘pK ‘PV ‘seproTiaq
"V ‘saptopjaqa.iag *229Q exe ST[EYS OY} JO ALT Se TRIE Ea he g-g ‘suowtoeds [oay] x1g |-a109] gassy ‘txeuetyy ——
ee
a
Mr. A. H. Cooke on Testaceous Mollusca
40
‘gouttoeds Jood opsuls B WOIT
paqttosap oq 0} you ynq ‘mou ATqIssog
‘payers ‘ATpeurpngrsuoy you ‘ATosoastiecy
OLB SYIL OY} Wooajod Sedtjs1ojUt oy} pu
‘snoyiqum ou st exoy3 ‘(00g “4 “4 ‘OORT
‘SIFT “JBN ‘SVT UNV) “PV “V JO BINp08
(wHpoy spivasoyye) gor ey} jou ATure41p
[een
-yuopt oq ATprvy wes pus ‘uor}rpu0s ae
Ut st VoUMIoeds opsurs ey} yng ‘you ATUIEILa_
“pypsn,fig
8 OAOV WOATS eSOT} ULI} UOTIPMOS os.t0A
v coyyer ut Ajuo “py "wy ‘vosnf Ajdutts
av s]jeys oy} {peyryuepr Apcuorm oy?
PV “V ‘82)
-noiow ,, 8B JjasmaTy suIBpy Aq peTfeqey ore
Koyg pur ‘os ore syjays yuesetd oy} Apureg
-10() | *(vasnf{-+-nynsnfig) Jo wutoy Sunok
ayy Ayduis st ‘poansy useq ToACU sey
gory. ‘seroods ey} yeq} worordsns suo.7ys
Aut pdooer Aus e1ozoroy} TTTM [ “SN
‘jag ey} ut edé} oY} LoACOSIP OF e]qe TAEq
jou oARy ] ‘Sumang ‘suzy oy} Woy (get “d
‘egg 'S ‘Z ‘d) supy 4q weats yonoyy,
“pprywu JO WOTZw.1E4[V
uese (egt ‘d “2st 9 WN ‘SZ ‘d)
yesmiy svsuy Aq eats ‘mAuouds royjour
yok st ‘seSuy “uuoufozy *xeoddestp
MOU OSTR ysnut e1ojoroy wsvbupy uoyedno
-ooard Jo punors oy} uo “svhup 07 wprpe
amen oy} patoyye (LJ8T “EL Wore “Use,
‘90g ‘Ao 001g) SpooAA-Wostuey, “T[9qs
"Sy IBULOY
"wag BUI)
wag BUIYD
[wyeqsny ‘g ‘under |’ -sourddimg
sourdd yy
‘ueder
[ying uvissog] ‘sourddymyg
= lie
"TOTINGIAASTT
‘memioads eg |**'* ‘pry ‘vy ‘e[nyIas ——
‘arey |" ‘pp ‘py “eyessnoep ——
[‘poutunteyop Mou
sv ‘Tommooun 40K |
"OYRIG
ee a | RE
‘oreyy | PEC ‘gosny
area | * “py VW “epypuea ——
i ane
‘rey |‘vosny | ‘py “py ‘epnyour ——
W224
vy ‘wosny=<] “py
‘aiBy | ‘“sliepnoroe ey[Laoqany,
TAS
41
obtained in the Gulf of Suez.
a
"rT ‘snwow eTqelIea
oy} JO "IVA B UY} eLOML SuTyZou ATqIssog
‘][VUIs pue Tory
-Ipmod peq UI St [ays ey} yuq | wnj7Aga.007
wourut0d 943 Jo sunok oy} ATao ATqeqorg
"409I10K)
‘ROTJIPMOD oTqissod 4s10M oY} UL
alv suotmtosds oy} {nyyquop AToutpesoxyy
“MOT}O9][OD OY} UL Mou stietUTOEds ON
‘poroaoostp st xode
qoojiod v JIM wotmweds v pun souvdeqe
Ur suleter uosenb oyy, ‘epmojzrtAqg
8Y} 0} FI SLoJoL J[PSMIIY suBpY * [HFZQnop
sl snues oy} Jo uoiisod ovurojsds ony,
"tof quesord oy} TILA [TOTS
ULIpeIsNYy-YN0G Bw seytyuept AT[nJyqnop
(91 ‘4 ‘cost ‘S"Z'd) seeuy “AO “tN
‘OT ‘A 'T4 “QLST “ISIH “FEN “ORI Y ‘aay
"qOO1IOKD)
‘sourddyiyg oy} pue wos
-yovpe ylog wor “py “Vy ‘vuawy nuohpy
O18 S][OYS OY} { UOVOHI}USpIsIUL ToYJoUW
‘sotoeds UMOTY
Aue unory ‘Aqyuoredde ‘pur vyuynuun worz
qourysip ajinb yno urny “4B pexooy ATesojo
Woy ‘sTTeys ey} ‘peynuepr ATHsey oor,
"LE ‘d ‘tA
‘OL8T “ISTH “FEN “OVI BY “Wuy Ur paqitosoqy
"4001109
SI WOVOHTUSp oy} Yey} wAyye youuvo T
‘suiotmioeds
[-esomio] ‘sourddymg joay {prop ‘faojem AMory |" '* *mog ‘canyetoseytq ——
[uepy] “veg poy
JN) UwIs19qg
sommddryig
['JJn9 urisiog| ‘ueder
‘Uv900 UBIPUy
ose Pee oe eee roo ee
‘sourddtyry
creer eerste too eee eo
[¢ Bly
-eIsny “S Gyn urvisiog] ‘ueder
[yy uetsi0g] ‘urder
“BOS BUILT)
[uosyour qxog ‘sourddyryg]
[‘sourddrryg ]
‘sT rqne
‘uvder
‘yuonberg {1oye MOT |**** ‘“mog ‘ummetnzeo
‘OVI JOU { *YYBT 19} 0} GALT | ‘Mog ‘osuetepe uINTyyLIE*D
‘WAMA LILO
‘uauttoeds oug |'* ‘pr ‘PF “epnprpuro ostyy
‘uauttoeds og |" * ‘pp "py ‘epLeyooruos
‘ds ‘u ‘uouroeds oug | ‘pr py “esoy[vo vutreytpAyg
‘areyy |" * ‘mog “eyepncueqns
‘area | *'*"* d mog “eordo
"TIEF OG Savy |" “pp Hy “eynoe vUNTTNGT
TY Ve
‘ds ‘u ‘uowoeds oug |‘isofeysoqy evurojsomeTvog
‘suomtoods OMY, | ‘VPP “e{VUIOID VUITNoUT_C
‘ds ‘u ‘uatatoeds oug |'* "°° * “pp ‘p “voata ——
jy
‘suotmweds mnog |p ‘xtpuey vurskydopdyq
‘suomteds omy, |'*"* ‘pp "Pp “eqysvo eraodq,
[PV
‘yp ‘eucowe eruodzy |
‘suouttoeds sary yy, | ‘py Pp “eAtny vursA,dou0 py
‘PY “V “eq8ep
‘suotmoods veayy, |-our [vimoAyy | vurjoonery
‘suotmtoeds mop |'* “pry ‘Pp ‘ByepnuUe eT[LOS—
‘ds ‘u ‘oreyy |°*'' eelpuvorpy epNULOy
‘usuttoeds emg |''** “py ‘py “eorpoum ——
Mr. A. H. Cooke on Testaceous Mollusca
42
Yor ysouomey ‘AmAuouds 044 poyeroumnus
sey (FE ‘ds ‘ossory Ivy Jop ‘ovpeyT) [ossT
“SAT “WMT oN} UL steumoeds ey} Jo
oumos poorrd suy Morpuyoryy { [Toys sty} JO
aDUB.G9[9 OY} JO BOP OU SaATS CINDY 8,0A001]
“omojeq ATyUEp
-TA9 suoumtoeds oseq} OIA 07 “pooAr
‘wnsobnt Jo wAMOUAS IOUT B ST 41 “oorI09
oq WOBoOHyIZUEPT oy JT Inq { poqitosep svar
“ysIOy “ungnnun ib oleyM MOU YOU OP T
‘MOTNGIAYSTp JO stod
-O1jOUL 9} UOT; eouRAstp Aq posnvo ‘wIOF
ad oy} moray Aovrouegep 03 enp oq wey)
JA 9218 Jo ssouljems oayeivduoo oly,
‘outg, ‘wnsoynpou jo AjetwA atom vB soaord
Ajayvur147M soroeds oy} Fr postadins oq jou
Teys [ ‘AySuorm asuauauyjhua soars Xq
-I9MOG $ (76g 'd ‘XI ‘JOA ‘IL “po “yo A ‘8 UW
UBT) asuauonyphca SI SuIT[Eds yOoIL09 ATT,
"MO
ee? a]qeirea oy} Jo utAuouds v ATUO =
(¢ 3g ‘1 -yd ‘TMEDQ “priqqy ees) soroeds
WUT, “Wa “unonayoy you Ayuwy109 ore
Aoy} Jey} ST TET, JO pres oq uUvd 4vq} Te
puv ‘suotatoeds uexorq very} ATUO ere O10,
‘pedoreaep Suteq yah you
YINoU Iystleyovrvyo oy} “MOG ‘wuwn70.17
-80.4 JO s]jeys sunod se poztusooer oq Avut
ynq ‘aortpuos s0od ut eave suowtoeds oT,
"SY IVUIOYT
“yuepunge
"Bog por |f oye MOTTEYS PUB LOTS
[3] qormpurg ‘uedee] ‘sourddiprgag | ‘oye1opour ‘1972 MoTTeYs
‘soutddrp1y q ‘adel § ‘TYRE XIG
‘soutdd py ‘area f peop ‘eroyg
[jee “voureg ‘sourddiyprqg
‘uojdeog ‘uoqinog] ‘«rBwose.cepeyy, ‘aetntoeds eto ‘atoyg
‘soutddriy gq ‘oret ‘peep ‘a1oyg
"Bag pory ‘oyetopoml {1097BA MOTT
"BOQ Pory ‘yuonborz {1078 MOTT
‘sourddipyg ‘arer $1078 MOTTRYG
‘stommtoeds
[‘uoqanog | jomy ‘prop {107@a ory
"MOTINGIUYST(T "MOTIRIG
sn ‘qyeddny ——
“''* noo ‘mINsoOont
"8" Mog Inze14801 ——
‘mog “uMNyeMoBUITTed
sone eee UT ‘ondouL
sees uae TNE}9e, ——
‘[pooyy ‘unsosnx]
‘ysiog “wnyRTNURLS
‘qu “camsor1eqny = |
WdT
sesee cen ‘qMoneTeIp ——
‘[ravog ‘umnyeI4801 |
aspag ‘oaTIOBls TUMTG LCA)
‘gsuoayyAre —— |
UMOP 408 BLOT} SI TOIUTpA ‘eungneee yng wg
-1unut You puy oM ‘Teasmoy ‘oeremnuy ,
91} 0} SULIeJeI UG ‘ApITVOCT BSB UROUBL
-I9}IPE, OY} SOALS pur “*[LOLg “Toy “wNUA
“ddytyg 0} seroeds oy} seqiiose oy (69 ‘ds
‘yMda) “AX “JOA) , BISOTOYOUOD , eyy UT
"So100ds 4S¥] SIT} I9AO OYVISIUT OT}STIOJORIBYD
B epeul sey sAseyy “MOG ‘wngyunu pue ‘oy PomMOYLN. seyy
“Mog ‘ungouoydis poppe eq 4snur T[oys ‘QI@I JOU SOTJOTIVA [RIOAOS
e[qvLIvA yeyMoutos siq} Jo AuAuouds oy OT, [oy ‘nomvg] ‘sourddryryg |‘teye moreys pue eroyg|'***** ‘og ‘euuntoo ——
‘[ smog
"UNILLIN TOF LOTTO TBOULOTO W [‘surmepuy] ‘sourddipiyg “TByeZ G § ore |cang11104 | iene —-
font rungobarwa A[qeyeystuun ore ‘[fong “unyesorrea |
\suoutoeds anoz oy} ‘peyuepr ApLomOT AA ‘sourddipin ‘oyerepour { peop ‘exoyg java ‘7 ‘uInye~notequy; ——
*| “aogy
‘euunyoo | chimes
‘mog ‘nuunjoo Jo uetmtoeds esiel W "sy Ajot00g |'ueutoeds ouo ‘prop ‘eroyg |'mog ‘uInyeuryoea = ——
*S10}09T[09
eures oy} Aq yysnoriq ‘ypaddnaz sv Ay1[R00T
eues oY} WO JI sears oy sv ATTeIoedse
‘SIq} We} PLOUL SUIGJOM st FI 4Vq Jorjeq
94} 0} OM spo] wnprquos Jo uotydiosep |
siddyiygq jo Apnys nyorvo @ pue “TIT
‘maddnay JO sui} JreAp Io sunok uoydeo
-X9 JHO}IM ore ‘cequunu ut AyueM} ynoqe
‘suouttoeds queseid ey, ,Uesunpriqqy ,
ey} UL peinsyg wnprqnos oy} extjan Ap1944n
pues ‘Aqiemog ‘wwunjoo Jo wo} & e¥IT
Ayqeytemer [Toys B 4L IoF soanoy ‘(GQRT)
,BIsoToyouoy, oy} Ul ssoy "Thd
‘wunprqvos ATWUEpL 07 eTqeun sem ‘(GggT) ‘Lua “Ted
snues oy} Jo ydeisouom stq ut ‘Aqiomog "eaQ pay |'e7vAepom ‘197VM MoTTRYS |-dnyy | 72/7 ‘wNpraqeos
‘soroeds queserd oy} T}TAA WOTXeu ; ga
-100 eyqissod ou eAvy vo pur ‘snbopla4 &
ST ‘MAOH [JOA ST sv ‘TeAoMOY “TOYS yeqJ,
‘OT “AL ‘]d ‘oT ‘TOUCH ‘eAcey UL MEATS SB
: | i )snqnynaiyin mmynwag seovyd ATsnorin9 oy
43
obtained in the Gulf of Suez.
Oe
[‘aeder "ST
: ‘sourddityg ‘susmepuy] -voupy “qf fleqne “yyy g-p fquonbeag fos + +++ + pyr yD0x ——
‘snupunivpy setoods oyexredes ot[} 07 UL
Toyteyg Aq opeur st yorym snznrosnf Jo ‘sy Teque “qyey
WLLOF 7Vq} 01 ATJovxa puodserr09 sTfeys ery, ‘soutddrigg |g {surat ‘suemtoeds omy | ‘Snug ‘SNYBLOSey SN.5e410 A
"wa “MOG ‘nuUunjoa= “Mog “unpnunu
JO WIOF Gorey B ATOTOUL stoes (WMO TOUT
-toeds oto ATWO stmaes etoy}) eTOYA v 8B
seroeds oy, “yWaeosauvad ore eerays porTVaed
94} STITT “poueyzcuerys ore se_npou pur
SQ eSIoASUBIY oY} Youd ut “TIE ‘eepjad
-dnay Jo vatoy B ATUO st uatMIOeds o[SuIs oY, theeE ate hricpehens lekereneneue ‘ered fey OALT |: + ‘Moy “uuntesTTUyyeds
‘qHOYSHo1gy oyvunyaoyum useq ‘wo ‘surou |
SVy M2ry 7a) 8894} JO UWOTyBoyTyUepT ety, ‘saurddryiyg ‘OIBI $ 1OYVA MOTTLIG fon ‘uanyesorres ——
tng ‘wines
-afyuoue ,, Sjavq ey} Wo ojou ve suy “Tea
‘snow ,, poreqet “sttyq ‘keuegq wo.y
‘SNP “JI oy} Ul yorquy W ‘ayqeysins
-Ulysipun oymb st yr yor wor ‘snvow ‘| wnry ‘sniom= ‘wary |
OL pesieut oq ysnur soroeds oy ue OLOFT [reven] ‘sourddyryg ‘Joye MoT yuonbeny |r wing ‘amrezow ——
*po.c.ouL
aq ysnun wnso.jad sotoeds YoITLAs Ut ‘poo AA ‘[pooyy ‘umsos
‘wneobnt Wor s[qeysinsuystpun 4m ‘soutddyiyg ‘toyWM MOT S4ueNbeLy |-nz] pooy, ‘umsoxed
‘OBI + 1O}VM MOTTRYS | “uamyerrysx9yUr WINTYILIED
‘soInjns 9 ‘nog |
4B Ino[oo Jo puvq ev Aq poyteur AyorrvA vB
St “TIyq faypungns opty “Mog ‘asewayore
-puns pues “Tyg ‘unonaypyp ore sutdu
-ouds LoyjIng ‘snues oy} Jo uoeuttoeds
UIOM pus plo AUB qsome xo Op yystur
gor. ‘(9 69) [[eYs ey Jo emsy puooes v
SHOSUL pur (‘snimesoyy,, ey} WoIZ ewngew
“nu Jo oinsy sAqraMaog satdoo oacexy 49K
jonig ‘uwngohjna jo Ayorwwa TIssoy B se
Mr. A. H. Cooke on Testaceous Mollusca
44
—————
a | A eS
"SHIVULOY “MOTNGLAYSTCT “MOT}R1G TEMS
1
<H
obtained in the Gulf of Suez.
*({1OYAA 4ST OT] TO *(poutmexe ore
__TOUIOY] IOUTOTH oYLory oystpoos orp ,, Jo ywods 07 spooooad rddryryq) suoTAIOEds JO LOYWINU e LOTA SOLIVA SUIT poye[NUVIS Jo Lequnuey}) snq
oyeu0 ‘sisouers ta9}dos sT][o}s09 OTITY[N ‘SISOUB.LS TAT}VLTesTqy TALoopoNp -Tyettesonburnb ouypn nyowyue ut ‘snqtettastyqns sttnuvis ¢ eredse
snqrjovrjue ‘eyBjoUNdroyUT OJNI TOA OATHF “eqs “eywUTUTNS’ ISO} “D -oyenurss ‘eyvjound-oosng snidees “eprqye ‘e}111N4-07vsU0T9 &489} (Q
“Mog “unaina—t way PID) ‘Ty “jaddnay wrnyp.0aQ
‘ST[OYS Os} OT} JO
suotdiosep oy ut syutod yoyyered Suryras erowm oy} eqMosMET} T ‘reoddestp 4snur wnainoas EUIeM EY} OSvd Loy} UT “(ZG Ties baeti Inj
<TqOSHto7 ‘QFRT) “Tal ‘ypeddner yim ‘op ¥ sv ‘odAy year oxy Apauepr osyo 10 “(RPST) “Hd “MON = (GEST) “MOS “wnatnore esvo YOrTaL Ty
‘ey ‘Sy sAqromog ‘zra ‘edA9 oy} ATTVOL JOU St Jey wnainoat Fo ad&q og sv preSor 0} reread Toyyre Avut oar : sn 07 Uedo sesino0d OA\4 oT aTOTY
Ajuenhesuog ‘suoToeT[09 Ut wees ATTeIOUAS sTToYs LomMyvuUt 94} ULOAT Atqecopismoo sagptp yor Jo Sunok oy} “Try “ypaddnay Jo uitoy sunod B
8B 4I SUIAJIUOPL UI UOTVLIISOY OU EAVT ] OU ELOJOY SOTIOS aSrey oy uroaz yng { wexporq Apaed dry coyno oy} WIL ‘uotutoods zood v st 47 ‘BUI
sAojaeyEy ‘ty ut Apzed ‘s Aqromog ut Apaed ‘odd oyg sv poyeur st [poys 1099vT sty ‘AjeyeUNgLoyUN “puy “41 WoAZ JOUT}STp eyinb st ‘yp “oy Jo
yeutsiz0 07} ‘toto oy} yng { (TY “Vyooy=) “MOG “uwnawse1 8B UOT AT[ensn TOYS OY} SI VT “ST j Setoeds yuetoyrp Oy OG 0} Jno UINy
Koy. pue ‘ow oxogoq Mou ore JT PUL QT ‘Soy sly orp Aqromog yor wo.1y s[poys penjor on} ‘sedAy oyy our quo] sey om ‘AoTUBTT “TJ JO
SHOTIPULY OY} ToNo1yy ‘MON ‘S[[OYS S,.cUrUIMs) Fo 9UO WOT, ST OT ‘Sy $27 ‘Sy st os ‘momoeTjoo sAcTuBPT “APA UL [TES B WOTF WABIp ST ‘yxeq
dy} UISN slo} oy SV ‘QT “Sty ‘19y}0 OY} UO “JT PU OT ‘s8y sty puv ‘puvy oo oy} Uo ‘QT “oY SITY Usomyod AyLIE[IUTISSIp eTyeytvaror ay} TILA
FONTS 4 0} [LBy JOUULD wHAWndaL NY RMA JO SEINSY g Aqromog sourmexe oy ovo Lue yng “ySnous opdunts oq pynoad coyqvur oy “TTP e1ew
SIT J] ‘o]qVUayUN uoTpUYstp oy} stoptiea podvpdsrp oxoy} suotuTdeds SNOIOTUNU OY} JO WONVUIMIEXS [NFoIvd B Inq “UMesN yp YS} oY} Ul JOULSTP
qdex ore soroeds ogy, ‘“(e sy ‘pl d “wuneypetaQ “It “TOA ‘redumprqqy ‘Tz 4 ‘Spel ‘ZoNereN IMF agosto, ‘tddipryg) wooy snbope4 wos
laquysthSaysrpun eymb st (gy ‘ZT ‘OT ‘s8y OG “d “wmnnyp2l4 “TE TOA “VtOTI9) » ‘KqIoMOG) snaumoat snbvja4 8B UOALe AT[BUSH TOYS oy, +
fein kk Rees a SS Ee ae
‘soroods ommes oy} oq 0} AToxI]
ATprey st quesoad oy} ‘vgouco weiseAvyso(y
oy} JO AqITVOOT ona, OY} 9 SOLPUT 280 AA
oy} JT ‘WOYeoyIUepr sty} Jo ssoujoos
-109 of} OUIWMeXe 0} 9[GQB Used JOU eABY J *SOIPUT “AA “TI8t OG-OT forerjont |***° °° *ysaqr “eyeuto
"Baum MON |'TICF OG-OT ‘ wouutoeds oug |***~** spuzr ‘suvolul ——
[-uedur
‘etuopeyeQ MON “BooeTeT) “eulyO * ‘qT OS-OT {exer | speagr “eqesnaz09 stzoqdtty,
‘saeat00 oq ATqtssod Avut
Jaoryeoytzuept eo} yey} st Aes uo ouO IIB
|yeq3 WoYyTpuoo peq Yous ut st wettoeds oY, ‘mpooury 110g ‘metmutoeds eu { ar0yg |****** “mogy onte, tanty91Ep
| [7e72@N | ‘omvd $eroyg|**** ‘aog “ejovryMOd BUT[OL/)
ST
' Teqne “yyezo[-g {yuenberg |**** ‘mogy ‘snArnoet | ——
Mr. A. H. Cooke on Testaceous Mollusca
46
qvy} OpNpouod 07 pay we 7] ‘e1eqAosTo pues
‘SU “GLIGE oY} UI yons se poytyuepr sTpeys
oy} JO ospe pue ‘suondriosep aAtjoodsor [-yeyeN ‘erpeqysny
Tey} FO uoreurMexe [nyervo AoA vB wor |A'N ‘ueder “esomso0g ‘uoqanog |
‘a10}
peyou souvreedde urepeorod ystmnyq ety
Ajjoexo Suryuoserd ‘snaneseyy, , 8 Aqtomog
Ud SUlTeq ‘aquaospsau ,, 0} pue “reg
‘suaosplauio poyTeqeyT ‘“snuyT “JMq eq} UL
ST[OYS 97} 0} spuodset100 47 + “peystuy exout
YOnUI efoOYA v SV TEYS ey} pus oyv10qBIa
910UL He SI einjdqnos oy} Yor ut “out
-peoeid oy} Jo Ayortea @ ATuO st soroeds sty, COS DS
"QUO SUOT4S B JOU ST
9889 STY 4VY} SNOTAQO st 41 ,‘paywouoye pus
Lopes e10U,, SI setoeds zong oy} 4eq} ST
AOA styy Fo yxoddns ur preaioy suliq Wed
ay soueragip ATwo oT} sous ynq { setoeds
ZING oy} JO ssouzoUtsIp oy} sproy (QeT “d
‘OSSOY “AVI [OP “OVTRIAL) [Oss] “papper
10 NOMWOD peT[VO aq 4 ToyJoyM ‘nyauaug
IO}VA-YSTYORIG UWvouVIIe}Ipeyy uoULUToD
oy} TAs Twouepr omw “yor WW “jog Aq
“pnoywmg se peqiiosep ‘sTTeys yueserd oT}
yey} st ‘taAemoy ‘eourytodurt Jo yutod ey,
‘OS SI JI 4G} Sutavtpeq ur Aytofear ey}
FO AOCM) Oye ay [Pou OLEUE If $ OSSTY ‘
pyoynuunu yt snouduouds st“aureq | [ydAony 07 oouvry "g Woy “UROTRI
‘pomoo JoyjOyM OF se JoyIp suotutdg |-toypeyy] ynH ueisieq “veg por
‘spurpy ‘sun?
NUP YIM yeoyuept stvodde soioeds ey], [-‘woqanog |
[‘yepAqm] “veg Baro
‘TwolyTept oq 0} stvedde “(got ‘d [ ‘woq
‘TOIUNary Op eB][,J ep ‘Youog) ‘ysoqy ‘vsow.wog |-tnoq] “puvjery MeN “ST TPOIApuRS
"SY IBULOY “MOTINGITIST(]
‘yuonbaiy ! 1eyea. MOTT
‘aL0ys WO JUBpUNngy
‘g1048 WO JUepuNnqy
[ ‘suatmtoeds nog |
"UPJ OS-OT f OBI JON
“WyeE OS-OL | erBY
"TOTYBIG
‘Lusog ‘snyeotns= }
‘ysaqr ‘SNTNOTACIG STxBUeT
. . sees ee ewe ‘dg
|
|
|
‘Lossy
‘eyeymouent) yout
§ Hog “wpneypreg eypeuertg |
‘sag “eyeyNUeloy —— |
‘anon § ‘py ‘eyeynueis ——
“* snug “eaqua stroqdrry,
TIP4S
vn
47
obtained in the Gulf of Suez.
Sg em RE Ps a a ee
jessy Aq WOALS T[EYs OURS OY} oq SNOT SIT,
“TIOM TONUL
[[@ ‘4stxe suemttoeds verqy A[UQ ‘suzy “IN
ey} ut st ody og} pus ‘WIIG "YW “A “AIT
Aq sngo.ysojound ‘gi ut peweu Aysurp
-10008 90 sTjeys juesatd ey, “eIs00
‘ongnaut) MOMMULOD oT} TIIM [vol}UEpt “TfEys
UVIPUT JSo AA B STSUUUpYW “W JO sngowroons ‘q
‘peytun sou ‘vynynpun pure nyopns ‘seroeds
omg jo mouy ATuo “(ye -d “xt ‘Elst “WN
pue ‘y) yno pezurod sey qyrurg se ‘yorvute’T
‘eM0 04 efqionper sv soroeds pouory
-Uel-9A0qe esey} [Te ‘op ] sv ‘paprcor
ey yey} curmoys ATurezd ‘soroeds zong uout
-ul0o9 ay} sv ATWO sngvojns spxooer (QQT “d
‘GOST “YOuOH ep “UIMofF) JUBTTVA pLTA
‘snaswih yim ahubrany sutdyyuept ‘4sSIT
BIQ-pey SIT UL snumayuayy pue snaseib
ATWO SEALS [SST IVY} pooy0U aq [ILM 4]
‘asessed Asva UB UWILO} OU eTOJeq sueut
-roeds oq} JO omos FOIyA 09 ‘YYpeerq AIO;
-1un etout jo Ayor1ea B ‘TITUTG ‘v.udsess.10
Ajqeqord pue “ayq ‘snumayuayy “o01g
‘snaswih exe stduiouds “uejrodumt ssey ynq
‘Tey}IN ‘“WoVtopod (F) ‘eovjans Jo ssou
-Y.snor 10 ssouq}oours (@) ‘seAoors jo ah
-unu (Zz) ‘seAoors 043 Jo yAdop (T) Jo yUI0
ut Ajword sommva sotoeds oy} yey} sos
suewoeds Auem jo uorjvulMexXe ue }eq}
Avs Ajdunts T]IM ynq ‘yoolqns oy} uo ots
-SHOSIP B OJUT 10309 0} o10y oovds Ou OAR
I ‘wog ‘snznojns poynqriystp-Ajepra pues
MWOMLUIOD OY} JO SOT}ELIVA o1OU o1e “YSECT
“huhriany pure ‘ysocy ‘snpnonag ‘wor 4304
abhi
@eeree ete cee or seve
[‘sves BuLyy |
‘peep ‘oawt {1e7eVm MOT |pP “P ‘snqoutoons
‘quonbory |'** * “woz ‘eonte snyeute A
‘HT CILENU A
‘| yquuy ‘snqetysojzound |
‘Lev
00g | ‘wor ‘snesits
‘[wwog ‘snqzeo
‘qguonboday {eye MOTT |-[ns = ]'ysaq‘tAuctAeg
eer eee coe eee
Mr. A. H. Cooke on Testaceous Mollusca
48
‘suotmtoeds ssoytnojoo puv ounoX ArT9A
ore Osoy} OIA Jo “uaryy ‘vsopn.10g Jo tA
-ouds O10 B SI 4T poyIyuept ATJOeIL00 e18
ST[OYS eset} JI ynq ‘ soroeds OY} AoUyY JOU Op T
‘NS0)NLO7Z JO SUETATOAdS PoTITRyS O18
STOYS oy} {[VUIpNyLSUOT arI4s ory ‘TOONS
aI SqIt oy} vynynununy ur Scmey} uodn
pue udeMyoq MIIjS OSIOASURI] OT] TTA
Yonod otvsqitoyy : vpuvjnununy you ATare,10—9
‘moljsonb ory
9]}798 0} eTGe Teeq you eAvy yng “ueT
‘ngnonsig= “ueryy ‘vsojn1og yey) yoodsns T
ere oeoeeroeoe se otoe
penne
-uopr Ayysre yur 7 mq “eqs cunok vy
‘sourddrry |
sourddrr |
[soutddrpryg ‘suoysuozy Svooryeyy |
(VISoTOyou , of} UL It poy
-IJUEPI jou svy erooyy = “ABs yOuTRO | SIq}
jo wiuouds vB si “pny “punwor 1yyoy MA
: "MOG ‘seswaosopmu ale s{jeys ey, apace eS Tae:
‘TOLVOYL}UEPT sty} JO
SsoU}OOIIOD OY} ooJUVIeN.S 07 9[qB Jou We T
“Avs
0} eTqvun we T ‘[voryuopt ere soroeds omy
0Y} LoqJOYM IO “ooLI0D st MOTyROyTUEpT
yorym {'yonory ‘sngadour srquopnduay se
eoeoereseos ee eo eae
“SYLVULOY "MOTINGLUYST
"B9G poy |-uoo prq ut ‘suouttoeds omy |'wary
‘anaauy
‘commons Ape |. ‘py “eye~norpeues4 ——
‘[ wary “esopnt
‘suoumtoods OMT, |-03] ‘pr ‘AT “Bq[ex
‘L-uaryy “esopn.104 |
: OY
‘eqenmMey =——
“T}EF OS-GI UE oteA JON | ‘Waxy “esoTN104 BTToYAINY,
‘W CITIALIWUD,
[-uotatoeds ou | | ‘Lasvay “eye4s000]]ru1 ] ——
[-sunod ‘touttoeds aug] |'*"* — “aagy “eqRT[NG~. ——
[-‘suommtoeds omy, | "°°" ++ “aogy “eth[~ ——
“yuonboay AToyetopoy, |' °° * “ogy “eyvoTnoe. 4 ——
‘[‘aog ‘ststte0.10p
‘suotatoods ueAeg |-ULUL) ‘pnp “Ipxeutor
‘suoumtoeds OMY, |" * ‘pnp “lowssniay vlavpeog
‘HAILAV'IVOG
UOT}R1G TEAS
49
obtained in the Gulf of Suez.
‘6
UNLISNDY DPA, “JX qanystp oy Azid v
sdeyazed st 41 “payst[quqse 19}30q 94} euT0Deq
SUI OUIVE 1949R] OYy se NET ‘CERT UL vM«
OULD PUe “TFRT UL Peqrtosop svar 41 SB
‘Aqttorad oy} eavy sqysta Mq pmnoys oueu
oy ‘(veg pay oy} wo osTe) ‘poexy
‘pjox YjIA Jeoryuspr sev ‘oavary ‘np«
“OULU Plecet T ‘suouttoeds Ay IOAO
‘oyuoyy § ‘apuajounbuns poyjaqry Aojeq
STTPYS otf} YyIM ‘oureq ote ‘MoT09T[00 ayy ‘| aaaagy |
ar poqueserder ATasaey AoA st sotoods sry, PRRs Gosh ga ‘yuonbery ‘aeyem mort | ‘yoar ‘eyRa0WAeUT
“SULIMOTOD JUALEBIpP yey
-oulos pue ortds poster At0A B 1QTA\ AjOITBA
poyTVUr-TjoM ev sv sould 971 oey OsTR plnoys
‘eavary “vurbnajo A{qeqorg “eyjewanyjoo ey}
SUIVSV VEY TOOLS OY} Jo ToJOVIVYD OT
UL pur ‘T3097 ey} Jo MoTIsod pur ‘requinu
‘edvys ory ‘Suryrvm oft pue yoryq poydna
-19}UL O1Stloyovtygo oy} ut ATIvpnoyced
‘soInyeoy [BLoMed Tey} UL sede [Le sotoods
pe][B9-0s esoyy ‘sqrt Jo ssauynoys pur ‘eatds
JO WoyvAsye “uoTyexojoo se sjutod xoutcE
{Ons Ur toyjOUY oO WHOA SULIOPICE “ry 00.17
-$2/ T}LM Tvorjuopt rveddy Tye Aoyy ‘Aoqyacn yy
‘621d SPST pur ‘ord TFeq ‘oumertorany
‘20G "JOOZ “Ae oy} UT poqidosep [je pur
‘SOLpuy “Gf OY} Wory [Te “poory ‘oumpew pure
“poor ‘vsobn.iwuas “Toor ‘nucojsoshya “ [Oo
‘punoyINy aT pure sotoeds styy weeayeq LZ ‘omysty |
soueeyiIp pyvaA ou ou o} savedde o1zoqy, [Teen ‘sourddipiyg] ‘veg poy “TOYVM MOTT [uray ‘topoortpenb ——
‘uepy 7 ATwowUIOD osTe sin900
yorya ‘edAz yg Jo wrtoy yyems v Ayorour
are qnq ‘Ajorea 4vy} 0} woAe puodser109
jou op ‘teAsmoy ‘sTfeys yuesead oyy, “T aes,
‘oyyod Jo Aporxrea peytvul-ToM B ynq SuUryy [even ‘erpeaysiny [awa ory “qty
Aue sv “poy ‘nyduny pavdox youu J | ‘oxodeSurg ‘uopy| ‘sourddyryg ‘IOYVM MOT f erVI JON |-od | ‘aaar ‘trqduanyy, eye Ny
“a CILIUAN
Ann. & Mag. N. Hist. Ser. 5. Vol, xvi.
Testaceous Mollusca obtained in the Gulf of Suez.
50
mAtouds B st “Ayu fy ‘vunrg.Laanog
“‘punibuney WIA you nq
‘sypiled YY apPNAT SOGTUOPT OL ¢ VU
uns wuud,, oq OF ‘edomoy ‘41 SUTyITUE
«pe ‘sypaid wory JouNsIp I sdeoy toysn-y
GIP ‘d “YEBT *X ‘seouspog sep ‘TIMq “4
ul Suey Aq sypeua JO “IBA B SB peqtios
-op Ayjeursiio sem pue ‘uuouds & st
‘(TPS ‘ANQ 20g "1007, "AexT) "Tooy ‘umwbumer
‘SULLOF O}BIPOULIAZUI oT} JO
doy oy} Woy}TM sotoeds ous oY} sv poztu
-Sooad 9q OU prnom puv ‘e[jeuNJoo eT}
TO sny[vo Suors vB WII ‘yory} AL-ouTpeed
-xo ore sueutoeds po Aqoa optya ‘paqqtt
Aydxeys pue urqy ety sunoX oy} ¢ u0rzE4s
Tey} 0} Surproooe ssoTJquop ‘ainyxXe} Ut
Ajepra aeyip [ywapoumbuns + vyp.couore |
seroeds e[qvuea Area sty} Jo suouttoodg
‘TILoy pomngdqnes reyjoq pue pernojod
zoyqsirq @ Aydunis st qt ‘soroeds curpooead
oy} wodg ATTeYUEsse SuTLeyIp yoodsea ou uy
‘snomAuouds
sivedde ‘veg poy ey} Wor os[e ‘eAvotyT
——
“SVU,
[‘pentityu09 aq oy, |
[40.4
edey ‘uosyour ytog] “JID UeIsIog» | wae 0G-0G “uenbeazun yoy | ‘svhup “Vuuttoyornd
OCC ir er et ee ST
é umnop
[yg semtog, ‘sourddyryg | |guenbory f yyez eg 07 e10yG |-AF ‘“YoTTMegq vrpsvaetg
_————<—$ $$
‘[aaaaiy “ey8acountvur = |
‘gied you f1dyVa Mory layevazpy “ey MeTOUINCURs ByLLA Ny
bbe oto bbe tb bo bo tb
a a ne | pe —
ane
“MONG LST LORS TENS
Mr. A. G. Butler on Doratopteryx of Rogenhofer. 51
V.—On. Doratopteryx of Rogenhofer, a Genus of Moths
allied to Himantopterus. By ArtHurG. BUTLER, F.L.S.,
F.Z.S., &e.
In my recent description of a new genus—Pedoptila, allied to
Himantopterus—I referred (pp. 840 and 342) to a moth from
Zanzibar identified many years since by Herr A. Rogenhofer
as a [Himantopterus, of which, however, no description
appeared to have been published.
Herr Rogenhofer has kindly forwarded to me a separate copy
of ashort paper, published last year in the ‘ Sitzungsberichten
der k. k. zoolog.-botanischen Gesellschaft in Wien’ (vol.
XXxiil.), in which a description of this moth appears, a new
genus, Doratopteryx, being erected for its reception. Although,
as I expected, this moth comes nearer to Pedoptila than to -
Himantopterus, it must stand as a distinct genus between
these two.
Doratopteryx, as figured and described by Herr Rogenhofer,
differs from Pedoptila as follows :—
Doratopteryx.
Expanse of wings 17 millim.
Secondaries 17 millim.
Costal and subcostal veins of pri-
maries well separated.
Subcostal branches separate at
their origins.
Lower radial and third median
well separated at their
origins,
Pedoptila.
Expanse of wings 23 millim.
Secondaries 183 millim.
Costal and subcostal veins of pri-
maries lying close together.
Subcostal branches emitted from
a short footstalk.
Lower radial and third median
from the same point.
Secondaries with three veins.
Secondaries with two veins.
_ These characters are all easily seen; but others are indi- -
cated which have rather a specific than a generic value, such
as the form of the outer margin of the primaries, which in
Doratopteryx is slightly sinuous (geschwungen), whereas in
Pedoptila it is regularly arched, the slightly shorter inner
margin of these wings in the former genus and the different
coloration, the type of Doratopteryx having the wings smoky
brown, with the basal area golden yellow, whereas Pedoptila
is grey, with the base bright russet reddish.
One difference which appears in the two figures is due to
an injury to the type of Pedoptila. In Doratopteryx the first
subcostal branch forks into two towards the apex ; this has,
however, clearly been the case with Pedoptila, only the apical
portion of both primaries in Mr. Swanzy’s specimen is broken
59, Mr. A. G. Butler on the Blue-belted Species
away, so that only the commencement of the fork is visible
on one side with the help of a lens.
I cannot at all agree with Herr Rogenhofer in his view that
these genera should be placed near to Procris; the entire
structure is, in my opinion, that of the Chalcosiide, and,
indeed, we have an unnamed genus in the Museum, unfortu-
nately without any indication of locality, which is distinctly -
intermediate between Pedoptila and Agalope, being almost of
the form of the latter ; but not at all widely differing from the
former in neuration, excepting that there are several cross-veins
(three on one side and four on the other) uniting the costal
vein of primaries to the costal margin, and that the subcostal
vein has the normal number (five) of branches.
Mr. M‘Lachlan, who examined the type of Himantopterus
and described its structure in the Belgian ‘ Entomological
Annals’ for 1877, kindly forwarded to me his very careful
sketches; I, however, failed to note in his sketch of the
hind wings the discocellular vein of his description :— Hl
n’existe pas de réticulation transversale, excepté une seule
veinule discoidale.” I regard the presence of this veinlet as
most important, since it proves the existence, in however
rudimentary a condition they may be, of the subcostal and
median veins, neither of which are, however, represented in
the published figures or even referred to.
In my figure of Pedoptila I see that the engraver has trans-
posed the numbers 7, thus giving the impression that the
moth is twice the size of the woodeut. I failed to note this
error on the proof of the cut.
VI.— On the Blue-belted Species of the Butierfly-genus Prothoé.
By Arruur G. Butter, F.L.8., F.Z.8., &e.
THE genus Prothoé has hitherto been supposed to contain
only one blue-belted species, Prothoé Franck (subsequently
corrected to Franckiz) of Godart’s ‘ Encyclopédie.’
Prothoé Franckit was described in 1819 from a single male
specimen received from Java; the diagnosis at the head of
the description runs as follows :—
““ Nym. alis subcaudatis, supra nigris: anticis fascia obliqua
alba azureo marginata : posticis subtus basi fusco inscriptis
apice virescenti pulverulentis.” ‘
Hiibner, in his ‘Sammlung exotischer Schmetterlinge,’
vol. ii, gives an admirable figure of the male, and Hewitson,
of the Butterfly-genus Prothoé. 53
in the ‘Genera of Diurnal Lepidoptera,’ a very fair figure of
the female.
In the museum collection there are four examples of the
Javan species, two males and two females, collected by Dr.
Horsfield; a fifth specimen, without locality-label, stands in
the Hewitson collection as the female of an allied species,
although it is im fact a male.
In 1854 the museum purchased a specimen of a Prothoé in
a mixed collection of insects from various localities, but bearing
no definite indication as to whence it came ; itis likely enough
to be the missing Malacca form which Mr. Distant quotes on
the authority of Wallace. This local form or species stood
in the museum for many years as the supposed male of Prothoé
Franckii; and consequently when, in 1867, and again in
1882, we received specimens of a third species from Borneo
and Tenasserim, I for the time believed them to represent an
interesting variety of the male approaching the female in
coloration ; in the Hewitson collection are three examples of
the same form, evidently regarded by him as males of P.
Franckw (though the first in the series is a female).
In a collection received in 1880 from Dr. George Watt
and made by him in Manipur, was a male specimen of a
fourth species perfectly distinct from the three previously
received ; this species will be described in full in a paper
giving an account of Dr. Watt’s collection.
The four species may be separated as follows :—
a. Primaries above with the oblique belt moderately
broad (more so in the male than the female), cobalt-blue,
intersected by a broad white band; apical area of secon-
daries purplish brown ; prevalent colouring on external area
OmMseCOndaTies, HCLOW, BTCV s/c. sie ves slam depen eloure ties P. Franckii.
b. Oblique belt of primaries shining azure or greenish,
with a series of irregular white dashes to represent the
central belt; apical area of secondaries purplish black ;
prevalent colouring on external area of secondaries below
MLS GROOM» 5 ale ore oH NETO Hoc. Lo SUI CSe OGmInEe TS bmeG P. angelica.
¢. Oblique belt of primaries without white band or
spots, excepting upon the costal border; apical area and
external border of secondaries chocolate-brown.
ce. 1. Oblique belt moderately broad, greenish blue; secon-
daries elongated, asin P. Franckit, with well-marked caudal
appendage, apical markings white with bluish borders; pre-
valent colouring on external area of secondaries pinky
greyish ........ Sune. ea bird. bin ais St lon | oat es a P. uniforms.
c. 2. Oblique belt very broad, covering nearly half the
wing, three spots of the same colour at centre of external
border, only separated from the belt by a blackish submar-
ginal stripe ; secondaries decidedly shorter and less caudate,
apical markings blue; prevalent colouring on external area
greyish oliyaceous, black and green...........0:..0.+0% P. regalis.
54 Mr. S. H. Seudder on Mesozoic Cockroaches.
Of the above species P. Franckii, in spite of its conspicuous
white band, is almost the dullest ; the male is a little brighter
in colouring than the female, and has a slightly narrower
white band across the primaries, but does not otherwise differ.
It comes only from Java (five examples).
Even more dull in colour is P. uniformis, and the absence
of the white band makes it appear more sombre than it really
is. It differs in many respects from P. Franckii, the greater
portion of the outer edge of the blue belt being occupied by a
long shallow sinus instead of being acutely zigzag; some of
the markings on the under surface are also confluent and the
discoidal spots are clearer in outline. I can only guess at
the probable habitat, as at present we only possess one male.
P. angelica is the brightest of all, the female being slightly
less so than the male; the blue belt is sometimes a little wider
than in P. Franckii and its outer edge is much less zigzag ;
it has white dashes on the belt in both sexes; the markings
below are very similar, but the ground-colour is noticeably
different. It occurs in Tenasserim, Borneo, and Sumatra
(five examples).
P. regalis is duller in colouring than the preceding, and
corresponds with P. wniformis in the absence of white on the
blue belt ; it, however, differs from the three preceding species
in the great width of the blue belt, the blue marginal spots on
the primaries, the shorter and less caudate secondaries, the
cruciform character of the black submarginal markings on
under surface of primaries, the filled-in discoidal markings ~
on all the wings, the inner half of external area of secondaries
below being greyish olivaceous crossed by oblong black
patches with reddish external borders, the shorter green and
black submarginal arched spots, and several other characters
to be described hereafter. I have only seen one male of this
very distinct species, from Manipur.
VII.—Notes on Mesozoic Cockroaches.
By Samvuet H. ScuppEr*.
J. Pterinoblattina, a remarkable Type of Paleoblattarie.
Among the many fossil cockroaches figured by Westwood
thirty years ago was one which Giebel afterwards named
Blatta pluma, on account of the resemblance of its neuration
to the barbs of a feather, where the shaft is on one side.
Several species are now known, and on account of this curious
arrangement of the veins, the generic name
* From the Proc. Acad. Nat. Sci. Philad, 1885, pp. 105-115,
Ct
ox
Mr. S. H. Scudder on Mesozote Cockroaches.
PTERINOBLATTINA (aréptvos)
is proposed. The wings were very broad, expanding con-
siderably beyond the base, broadest beyond the middle, and
filled with an abundance of branching veins. The mediastinal,
scapular, and externomedian veins ran close together, side by
side, in a perfectly straight course (the shaft of the feather),
from near the middle of the base of the wing toward and nearly
to a point on the costal margin a little within the apex of the
wing, and the superior mediastinal and inferior externomedian
branches, crowded closely together, parted from this appa-
rently common stem at nearly similar angles on either side of
it. ‘The complete independence of the mediastinal, scapular,
and externomedian veins shows that the genus falls in the
Paleoblattarie. The species are all small.
Pterinoblattina pluma.
Blatia pluma, Gieb. Ins. der Vorw. p. 322. Figured by Westw. Quart.
Journ. Geol. Soc. Lond. x. pl. xv. fig. 14f.
The specimen, the original of which I have had the privi-
lege of studying, by the favour of my kind friend, the Rev.
P. B. Brodie, is rather imperfect, and a little deceptive from
the fact that just that portion of the tip is missing which con-
tains the scapular branches ; it is probable, however, from the
longitudinal character of the apical externomedian offshoots,
that the species more closely resembles P. chrysea than P.
éntermixta. All the mediastinal branches are simple, parallel,
equidistant, almest straight, closely. crowded, and part from
the main stem at an angle of about 45°. The externomedian
branches, the only others preserved, part at a less angle, gradu-
ally become quite horizontal apically, are nearly as close at
base as the scapular branches, and as most of them fork and
even refork, though with entire irregularity, become exces-
sively crowded towards the margin. ‘The length of the frag-
ment is 9 millim., its breadth 5 millim. Probably the wing
was 12 millim. long, and 5°5 millim. broad.
It was found in the Corbula or Pecten beds of the Dorset
Purbecks of England.
Pterinoblattina penna, sp. nov.
The single specimen of this species at hand is preserved in
much the same manner as the last, but shows a fragment of
the internomedian region. ‘The three principal veins approach
each other very gradually, so as to give them the appearance
of a tapering rod. The mediastinal branches part from the
stem at nearly a right angle near the base of the wing, gradu-
56 My. S. H. Scudder on Mesozoic Cockroaches.
ally increasing in obliquity distally until they form an angle
of 45° with it; they are slightly curved, the concavity out-
ward, very closely crowded, and about every third one forked
near the middle, but with no regularity. The scapular
branches are not preserved, but as in P. pluma, and for the
same reason, they probably resemble P. chrysea rather than
P. intermixta. The externomedian branches are very closely
crowded, generally straight, part from the stem at an angle
of 45° next the base, and become almost wholly longitudinal
at the apex; they fork about as frequently as, and more irre-
gularly than, the mediastinal branches. The internomedian
area extends far out on the wing, and its branches (what few
can be seen) resemble those of the preceding area, and at its
extremity are parallel to them. Length of fragment 13
millim., width 9 millim. ; probable length of wing 15 millim.,
probable width 9 millim.
Described from a specimen from the English Purbecks
‘sent me for examination by Rev. P. B. Brodie.
It is not impossible that the fragment of a larger wing
figured by Westwood (Quart. Journ. Geol. Soc. Lond. 1854,
pl. xvii. fig. 7), from the Lower Purbecks of Durdlestone Bay,
may be a species very close to this.
Pterinoblattina chrysea.
Blattina chrysea, K. Geinitz, Zeitschr. deutsch. geol. Gesellsch. 1880,
p. 520, pl. xxxil. fig. 2.
In this case we have a more perfect wing, the tip being
almost completely preserved. ‘The mediastinal vein termi-
nates before the middle of the outer half of the costal border,
and is furnished with simple, straight, oblique branches, not
so numerous as in the other species, to judge by the figure,
though they are spoken of by Geinitz as “ very numerous
and closely crowded.” Just before the scapular reaches the
tip of the mediastinal, it turns parallel to the costal margin,
runs to the upper tip of the wing, and emits branches similar
to those of the mediastinal, but of course of equal length. All
the externomedian branches run almost longitudinally, are
straight, sometimes forked, and appear from the figure to be
less crowded than the mediastinal branches, though they are
compared by Geinitz to the barbs of a feather. The interno-
median runs to just beyond the broadest part of the wing,
being thus longer than the mediastinal, and sends less crowded,
gently curved, usually forked, rather short branches to the
border. ‘The few anal branches curve and strike the inner
margin. Length 5 millim., breadth about 2°25 millim,
Mr. S. H. Scudder on Mesozote Cockroaches. Sil
From the Lias of Dobbertin, Germany. The description
is drawn up from the data given by Geinitz.
Pterinoblattina intermixta, sp. nov.
A nearly complete wing of this species has almost the same
shape as P. chrysea, but the upper part of the apex is more
produced. The mediastinal vein terminates before the middle
of the outer half of the wing, and the area narrows more
gradually than in any of the others; its branches are gently
curved, and often forked, but not excessively crowded. Just
before reaching the tip of the mediastinal the scapular vein
suddenly bends towards the apex, running subparallel to, but
away from, the costal margin, terminating at the tip and
emitting a crowd of curved and forked branches, The closely
crowded externomedian branches part at an angle of 45°
with the stem, are straight, and forked only just before the
tip, forming a tolerably regular belt of crowded veinlets along
the margin. The basal branches, however, are interfered with
and affected by the internomedian vein, which is nearly
straight, at first running plump against the externomedian
branches, curves then downward parallel to these, and termi-
nates a little before the mediastinal; it is furnished abun-
dantly with branches curving like its extremity and branching
next the border like the externomedian branches; but where
it abuts against these latter they simulate the appearance of
ihe internomedian branches so as to appear as if a part of the
internomedian area, and thus give the latter the appearance
of extending out beyond the broadest part of the wing. The
anal appears to be insignificant, reaching less than a third the
distance from the base, and resembling a narrower and smaller
internomedian area. Length of fragment 10°5 millim., pro-
bable length of wing 12 millim.
Received from Rev. P. B. Brodie, as coming from the
Upper Lias of Alderton, Gloucestershire, England.
Pierinoblattina hospes.
Ricania hospes, Germ. Acta Acad. Leop. Carol. xix. pp. 220, 221,
pl. xxii. fig. 18. :
Germar took this for one of the Fulgorina, in the neigh-
- bourhood of Ricania and Peciloptera. It is pretty plain, how-
ever, that it belongs here, though the figure given by Germar
is not sufficiently clear to enable one to formulate any charac-
teristics. Assmann thought it a Neuropteron, falling in the
neighbourhood of Drepanopteryz.
It comes from the Oolite of Solenhofen.
58 Mr. 8. H. Scudder on Mesozoic Cockroaches.
Pterinoblattina gigas.
Ricania gigas, Weyenb. Arch. Mus. Teyl. ii. pp. 270, 271, pl. xxxv.
fig, 23.
Following Germar, Weyenbergh placed this enormous
species in ftcania; but it as evidently falls here and bears
a close general resemblance, excepting in size, to P. penna of
the Purbecks. Ricania fulgens, Gieb. (Brodie, pl. iv. fig. 12),
from the Vale of Wardour, has nothing to do with Pterino-
blattina.
This gigantic form also comes from the Oolite of Solenhofen.
Il. Triassic Blattarice from Colorado.
In a recent paper I described some of the Triassic Palzeo-
blattariz, which I mentioned as interesting on account of
their special relation to the Blattarizee of the same formation.
Brief diagnoses of these latter forms will therefore have some
interest, and I mention them in the order of their relation to
the Paleoblattarie.
NEORTHROBLATTINA (véos, dpOpus), gen. nov.
In this genus the wings are about two and a half times
longer than broad, with fairly well-rounded apices, the medi-
astinal and scapular veins amalgamated into a single vein,
which extends nearly to the tip, and in the middle of the
wing occupies nearly one kalf its width. The internomedian
vein is of varying importance, and in the large anal area the
veinlets terminate on the margin ; the anal furrow is strongly
arcuate and deeply impressed.
Neorthroblattina albolineata, sp. nov.
The single wing has lost the tip, but all the essential fea-
tures are preserved excepting the form of the tip. The wing
is very dark-coloured, and the veins appear as very pale lines
upon it. The costal margin is gently and equably arched,
while the inner margin is perfectly straight. The externo-
median vein is little developed, first forking, and then not
widely, in the middle of the wing, its fuller development
being prevented by the ample and unrestricted development
of the internomedian vein, which runs in a full rounded course
nearly to the tip of the wing. The anal area is interesting
because the veins of the upper half run close to, but do not
impinge upon, the anal furrow, curving downward just before
reaching it, and either running into the next vein below and
terminating there, or continuing parallel to the furrow and
terminating on the inner border. Length of fragment 7
Mr. S. H. Scudder on Mesozote Cockroaches. 59
millim. ; probable length of wing 9 millim. ; breadth of wing
3°5 millim.
Triassic beds near Fairplay, Colorado.
Neorthroblattina Lakes, sp. nov.
Several specimens of this species were found. The costal
margin is arched, as in the last species, and the inner margin
has an almost equal opposite curvature. The externomedian
vein has a very sinuous course, and forks before the middle
of the wing with abundant neuration, occupying on the mar-
gin the entire tip of the wing and almost the outer half of the
lower margin, while the internomedian is reduced to an arching
vein, extending but little beyond the anal furrow, and with
only two or three branches ; the anal veins are all parallel to
the anal furrow and simple. Length of wing 9 millim. ;
breadth 3°5 millim.
Triassic beds near Fairplay, Colorado.
This species is named after Prof. Arthur Lakes, of the
School of Mines in Golden, Colorado, who first made known
these beds, this species being one of the first discovered
by him.
Neorthroblattina rotundata, sp. nov.
The costal margin in this species is very strongly arched,
while the inner margin is straight, giving a very different
aspect tothe wing. It closely resembles the preceding species
in the mediastmo-scapular and anal areas, and also in the
peculiarities of the externomedian vein, excepting that the
latter does not encroach to so large a degree upon the interno-
median, the terminal offshoot of which creeps along the border
so as to limit the marginal extent of the externomedian area
almost as much below as above, although the branching of
the externomedian vein is scarcely lessened. Length of wing
8°5 millim.; breadth 3°3 millim.
Triassic beds near Fairplay, Colorado.
Neorthroblattina attenuata, sp. nov.
This species departs from the typical forms in its slender-
ness and pointed apex, but it agrees so fairly in general
structure that it would best be placed here. The costal
margin is not regularly arched, being flattened mesially,
while the whole wing tapers beyond the basal third; the
inner margin is also arcuate, and the tip bluntly pointed.
The mediastino-scapular vein terminates considerably before
the apex, and the oppositely arcuate internomedian reaches
60 Mr. 8S. H. Scudder on Mesozoic Cockroaches.
almost as far out, the branches of both nearly always simple.
The anal veins are only slightly irregular. Length of wing
15 millim.; breadth 4 millim.
Triassic beds near Fairplay, Colorado.
SCUTINOBLATTINA (cKUTUVOS), gen. Nov.
In this genus, composed of small species, the front wings
are decidedly more coriaceous than the hind wings, so that
the neuration is often more or less obscured by it. The wing
itself is convex, as in the modern Phoraspis, and subtriangular
in form, its greatest width being near the base, while the tip
is bluntly pointed. ‘The mediastinal and scapular veins are
again blended into one, which, instead of having a sinuous
course, 1s nearly or quite straight, and terminates below the
apex of the wing, while the externomedian vein follows
closely parallel to it, and the oblique veins of this and the
internomedian veins follow each other so as to make it diffi-
cult to tell where the line of demarcation may lie. The anal
veins sometimes fall on the margin and sometimes on the
anal furrow.
Scutinoblattina Brongniarti, sp. nov.
In this interesting species the wings are very strongly
convex at the base and the whole surface is flecked with dark
spots. The branches part from the main veins at a similar
angle on either side of the middle of the wing. The anal
area extends nearly to the middle of the wing, where it is
marked by a considerable emargination, and its veins are
frequent, oblique, mostly simple, and terminate on the margin.
Length of wing 7 millim. ; breadth 3 millim.
Triassic beds near Fairplay, Colorado.
Named after Mr. Charles Brongniart, of Paris, well known
for his remarkable discoveries among the older fossil insects.
Scutinoblattina intermedia, sp. nov.
This species resembles the last, but is not marked by any
dots, and the anal area, while shorter, shows no emargination
of the border at its extremity ; the anal veins are very close,
parallel to the inner margin, and terminate not on the margin,
but on theanal furrow. It further differs in that the externo-
median branches are considerably more longitudinal than
those terminating on the costal margin. Length of wing
7 millim.; breadth 2°75 millim.
Triassic beds near Fairplay, Colorado.
>
Mr. 8. H. Scudder on Mesozote Cockroaches. 61
Scutinoblattina recta, Sp. Nov.
This species, the smallest and most abundant of all in the
Triassic rocks, is rather slenderer than the others, and has the
surface finely reticulated. The mediastino-scapular and
externomedian veins run side by side in perfectly straight
lines from the middle of the base to the middle of the tip, the
branches, very few in number, parting similarly on the two
sides. ‘The costal is more arched than the inner margin, and
where they can be made out the one or two anal veins seem
to run to the margin; but all the veins on the wing are
exceedingly obscure. Length of wing 6:3 millim.; breadth
2-4 millim,
Triassic beds near Fairplay, Colorado.
III. On the Genera hitherto proposed for Mesozoic Blattarie.
Brodie, in 1845, published figures of a considerable number
of Mesozoic cockroaches, but named only one, which he
referred to the genus Blatta. In 1852 Heer figured and
named another under the equally broad generic name Blat-
tina. Westwood, in publishing in 1854 a considerable
addition to our knowledge of the cockroaches of the English
Mesozoic rocks, separated four somewhat peculiar forms under
the generic term Blattidiwm ; the rest were unnamed. Giebel,
two years later, named a considerable proportion of Brodie’s
and Westwood’s species ; while placing a considerable num-
ber under Blatta and Blatiina, he divided the rest under three
new genera—livthma, Hlisama, and Nethania—the last in-
cluding the only one of Westwood’s species of Blattidium
which was noticed. On the other hand, Heer, in 1864,
divided all the Mesozoic species between Blattina and Blat-
tidium, placing in the latter all of Westwood’s species,
together with all those referred to new genera by Giebel.
Finally, a few years ago, HE. Geinitz proposed for a Triassic
species described by him, and one previously published by
Heer, the new generic term JMesobdlattina.
There is no question that the forms described by West-
wood, after eliminating the one separated by Giebel under
the name of Nethania, form a very distinct group ; but none
of the species since added to it belong here, so that
BLATTIDIUM
should stand much as first limited (though not described) by
Westwood. Probably, however, it should be still further
restricted by the elimination of B. achelous, Westwood. The
62 Mr. S. H. Scudder on MWesozote Cockroaches.
wings are exceedingly long and slender, particularly in B.
symyrus, Westw. (which may be taken as the type), with
nearly or quite parallel sides. The mediastinal vein termi-
nates not far from the middle of the wing, and sends out a
multitude of crowded offshoots to the margin. The scapular
vein unites in the basal third of the wing with the externo-
median, and throws off rather distant oblique veins, first to
the mediastinal and afterwards to the border. The externo-
median and internomedian veins have together several more
or less forked very longitudinal branches, all of which appear
to terminate on the apical margin, while the main anal vein,
longitudinally oblique, extends nearly as far as the medias-
tinal, and the outer half of the inner margin of the wing
seems to have no veins falling upon it; the veins of the anal
area run obliquely from the margin upward and outward to
the main anal vein.
As to the genera of Giebel, six species are placed by him
in Rithma, two in LElisama, and one in Nethania. The
species of Nethania is rather too uncertainly figured to deter-
mine by the illustration alone where it belongs. The two
species of
E,LISAMA
figured by Brodie certainly belong together, and seem to con-
stitute a natural genus. By the kindness of the Rev. Mr.
Brodie I have seen the original of his pl. v. fig. 1 (Zlisama
Knert of Giebel) and another specimen which seems to belong
to E. minor, so that I can more fully characterize this genus.
The mediastinal and scapular veins appear here to constitute
one vein, and to occupy almost the entire upper half of the
wing. ‘The externomedian and internomedian veins fill the
lower half between them with parallel veins, which at their
origin curve at once strongly downward, and then run longi-
tudinally to the apical margin, leaving only the meagrest
possible space to the anal area, which is indeed broken off
from the two specimens I have seen, and does not appear in
the figures published by Brodie. In addition, in both the
species there is an abundant but imperfect cross-venation at
the base of the externomedian and internomedian areas, and
on the latter a large discoloured spot, which may of course be
confined to these two species only.
RITHMA
contains more incongruous material. I have myself recog-
nized in the English species I have examined autoptically
only one of the species referred to it, named A. Murchisont
Mr. S. H. Scudder on Mesozoic Cockroaches. 63
by Giebel, and this is certainly to be referred to Mesoblattina,
Geinitz. 2. ramificata is quite too imperfect to be considered
until better specimens occur. It is probable that &. antiqua
should be separated from the others, and the same may be
true of &. Westwoodi. This leaves two species, Rk. purbec-
censis and R. Morris’, which agree well together, and repre-
sent a group which seems to have flourished in Mesozoic
times, as I have seen a number of species from the English
Lias belonging to it; and Blattina formosa, Heer, from
Schambelen, and Slattina liasina, Gieb., figured by Brodie,
also belong here. These wings are rounded wedge-shaped,
with the amalgamated mediastinal and scapular area so large
as to occupy about half of the wing, the vein running in a
slightly sinuous course to, or even below, the tip. The anal
area is generally pretty large, convex, and filled with parallel
veins, which terminate on the margin. The space between
is divided about equally between the externomedian and
internomedian veins, which generally take a somewhat
sinuous course, and fork with tolerable abundance, filling the
space with graceful lines, spreading like (sinuous) rays of a
fan. The genus is closely related to Neorthroblattina of the
American Trias, but differs from it in the much greater area
covered by the amalgamated mediastinal and scapular veins.
The following described species may be referred to it :—
fithma purbeccensis.
Rithma purbeccensis, Gieb. Faun. d. Vorw. iii. p. 319. Figured by
Westw. Quart. Journ. Geol. Soc. Lond. x. pl. xviii. fig. 32.
Lower Purbecks, Durdlestone Bay, England.
Rithma Morrisi.
Rithma Morrisi, Gieb. Faun. d. Vorw. ii. p. 319. Figured by Westw.
Quart. Journ. Geol. Soc, Lond. x. pl. xvii. fig. 34.
Lower Purbecks, Durdlestone Bay, England.
Rithma formosa.
Blattina formosa, Heer, Lias Ins. Aarg. p. 15, pl. H. figs. 41, 42; id.
Urw. Schweiz. pl. vil fies. 1,16 a : iss
Lias, Schambelen, Switzerland.
Rithma l“asina.
Blattina liasina, Gieb. Faun. d. Vorw. iii. p. 317. Figured by Brodie,
Foss. Ins. Engl. pl. viii. fig. 12.
Lower Lias of Wainlode, Strensham, England.
64. Mr. S. H. Scudder on Mesozoie Cockroaches.
MESOBLATTINA,
proposed by E. Geinitz, as stated, for two Liassic species of
continental Europe, is a most prolific type, a considerable
number of English Mesozoic forms falling here, and among
others, as remarked above, those figured by Westwood and
described by Giebel under the name of Authma Murchisone
and R. antiqua. The former of these, as well as a consider-
able number of new species, have been sent to me by Mr.
Brodie. In this genus the basal sweep of the externomedian
and internomedian veins is very noticeable, following as they
do the curve of the anal furrow before branching to fill the
lower half of the wing. In this respect they remind one
strongly of Elisama; but the wings are much slenderer than
there, and, what is of more importance, the anal area is of
the normal size, while next the humeral angle is seen a flat
unveined field, so frequent in modern cockroaches. To this
belong, among others, the following species :—
Mesoblattina protypa.
Mesoblattina protypa, Gein. Zeitschr. deutsch. geol. Gesellsch. 1880,
pp. 019, 520, pl. xxii. fig. 1.
Lias of Dobbertin, Germany.
Mesoblattina angustata.
Mesoblattina angustata, Gein. Zeitschr. deutsch. geol. Gesellsch. 1880,
pp. 519, 520.
Blattina angustata, Heer, Viert. naturf. Gesell. Zurich, ix. pp. 288-
300, pl. fig. 6.
Lias of Schambelen, Switzerland.
Mesoblattina dobbertinensis, Gein.
Mesoblattina dobbertinensis, Gein. Zeitschr. deutsch. Geol. Gesellsch.
1884, p. 570, pl. xiii. fig. 1.
Lias of Dobbertin, Germany.
Mesoblattina Murchisoné.
Rithma Murchisoni, Gieb. Ins. d. Vorw. p. 319. Figured by Westw.
Quart. Journ. Geol. Soc. Lond. x. pl. xviii. fig. 43.
Lower Purbecks of Durdlestone Bay, England.
Mesoblattina antiqua.
Rithma antigua, Gieb. Ins. d. Vorw. p. 319. Figured by Westw.
Quart. Journ. Geol. Soc. Lond. x. pl. xvii. fig. 10.
Lower Purbecks of Durdlestone Bay, England.
Mesoblattina elongata.
Blatta elongata, Gieb. Ins. d. Vorw. p. 322. Figured by Westw. -
Quart. Journ. Geol. Soc. Lond. x. pl. xv. fig. 23.
Middle Purbecks of Durdlestone Bay, England.
Bibliographical Notices. 65
BIBLIOGRAPHICAL NOTICES.
The Birds of Lancashire. By F. 8. Mircuett.
Post 8vo. London: Van Voorst, 1885.
WE hail the appearance of Mr. F. 8. Mitchell’s neat and exhaustive
little handbook on ‘The Birds of Lancashire’ with great pleasure.
Previous to the issue of this work we possessed no standard infor-
mation of any kind in a collective form respecting the avifauna of
the vast district lying between the Bristol Channel and the Solway
Firth. This hiatus is keenly felt by those naturalists who have
occasion to work out the distribution of birds in the British Islands.
The west of England and the whole of Wales have been much
neglected by the “local naturalists ;” but we hope that the careful
observations made by Mr. Mitchell will prove contagious, and that
his useful handbook will be followed by similar works dealing with
the other western counties, until the birds are as well known and
their distribution as accurately determined as in the eastern
counties. Without aspiring to the pretensions of such works as
Stevenson’s ‘ Birds of Norfolk’ or Gray’s ‘ Birds of the West of
Scotland,’ Mr. Mitchell’s handbook supplies us with much informa-
tion which we fail to find in those more elaborate works. We
allude to the careful way in which the time of arrival and the
date at which each species lays its eggs is given—information which
will be of the highest service to many a young naturalist in the
northern counties. Nor will the numerous local names of birds be
less welcome to many readers. Much valuable information is given
respecting the occurrence of wild fowl on the coasts of a county
eminently suited to the requirements of such birds, which the shore-
shooter will do well to study ; and many “straight tips” and quiet
hints are given respecting the modes by which they are captured ;
whilst a considerable amount of interesting archeological informa-
tion is incorporated. The charming woodcuts by Whymper of the
“decoy pipes,” showing the method by which the wary ducks are
lured to their doom, are exceptionally realistic. In addition to
numerous woodcuts the work is embellished by two beautiful
coloured plates by Keulemans, one of the Black-throated Wheatear
(a bird which has hitherto only been met with in the United King-
dom in Lancashire), and the other of the Wall-Creeper. Several
occurrences of rare birds in the British Islands are here recorded
apparently for the first time; and not a few interesting particulars
are given concerning the habits of many species. We must doubt,
however, the correctness of Mr. Mitchell’s assertion that the Star-
ling is only single-brooded—in the adjoining county of York it
certainly rears two, if not three, broods in the season. Lancashire
compares most favourably with other counties with regard to its
avifauna, which we are told numbers 256 species. No less than
116 of these are given as breeding within the limits of the county,
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 5
66 Bibliographical Notices.
whilst 65 are winter visitors and 75 occasional visitors. The range
of each is carefully traced through the county, and the time of arrival,
nidification, number of broods, number of eggs, comparative abun-
dance, together with numerous notes of. local interest and peculi-
arities of habit, are given.
In short, Mr. Mitchell has performed his task well, and has
obviously been at much pains to render his information as complete
and reliable as possible. The work will be welcome and useful to
all who take an interest in British birds, and must prove indispen-
sable to the many north-country artisan-naturalists whose leisure
time from toil in noisy mill or factory is spent in studying natural
history in the suburbs of their crowded towns. We hope that
provincial naturalists will not rest until every county not yet
favoured with a handbook to its bird-life can boast of one planned
with as much care and carried out with as much completeness as
the useful and interesting little volume before us.
Memoirs of the Geological Survey of India. Palcontologia Indica,
being Figures and Descriptions of the Organic Remains procured
during the Progress of the Geological Survey of India. Published
by order of His Excellency the Governor-General of India in
Council. Series x. Indian Tertiary and Post-Tertiary Verte-
brata.—Vol. III. Part 1. Additional Siwalik Perissodactyla and
Proboscidia, with 5 plates and 6 woodcuts. Part 2. Stalk
and Narbada Bunodont Suina, with 7 plates and 1 woodeut.
Part 3. Rodents and new Ruminants from the Siwaliks, and
Synopsis of Mammalia, with 1 plate and 8 woodeuts. Part 4.
Siwalik Birds, with 2 plates. Part 5. Mastodon Teeth from
Perim Island, with 2 plates. By R. Lypexxmr, B.A., F.GS.,
F.Z.8. 4to. Calcutta: Geological Survey Office. London:
Triibner & Co. 1884.
Tur Memoirs included in Mr. Lydekker’s third volume of Indian
Tertiary Vertebrata are varied in matter and vary in importance.
We may say of the yolume as a whole, that it makes an important,
valuable, and welcome contribution to the knowledge of the subjects
of which it treats; and every anatomist will need to examine in
detail the materials described and discussed in the successively
issued parts of the work.
Part 1 opens with an account of Accratherium Blanfordi, founded
on materials collected by Mr. W. T. Blanford in the Lower Siwaliks
of the extreme west of India.
Upper molar teeth of two races of this rhinoceros are described,
which differ in size. Its affinities are with the Rhinoceros pale-
indicus, which, however, has the external surface of the molar teeth
flatter. The bases of the two colles are in contact in A. paleindicus,
and that species wants the tubercle at the entrance to the median
valley. The distinction of A. Blanfordi from Rhinoceros sivalensis
Bibliographical Notices. 67
is found in that species having the second costa of the molar teeth
more prominent, in the anterior collis having no vertical groove
on its posterior side, in the ante-crotchet of A. Blanfordi being
absent, while the crotchet is relatively larger. The molar teeth of
Aceratherium perimense are distinguished from those of A. Blanfordi
by greater development of the buttress and costa, while the ante-
crotchet is less developed, and the posterior valley forms a deep pit
instead of a slit. Figures are given of the mandible, showing its
general form, and indicating that the symphysis approximated to
the characters of the Javan rhinoceros.
The lower molars have a faint trace of an external cingulum.
After comparing this Indian fossil with other species of rhinoceros,
the author concludes that there is a strong presumption that it is
an Aceratherium, though it is difficult at present to establish distinc-
tion from its American allies. The two races are distinguished
as majus and minus. Among Kuropean types it finds its nearest
ally in A. inciswwum; and the Rhinoceros deccanensis is thought to
have been a descendant from the same stock as Aceratherium Blan-
ordi.
- Hipparion antilopmum has a cranium referred to it from the
Siwaliks of Perim Island, in which the teeth exhibit the com-
plete isolation of the anterior pillar characteristic of Hipparion,
though the pillar is less elongated than in the teeth referred to H.
Theobaldi. Still, the skull is only determined provisionally, and is
compared with H. gracile, with the conclusion that the form of the
posterior maxillary cavity establishes a specific distinction. Other
teeth from Perim Island are described, and if they prove to belong
to a new species it may be named JH, Feddeni.
The remainder of the memoir is devoted to Mastodons. Three
tretalophodont species and two trilophodont species have been
already described from the Siwaliks, and the author now indi-
cates trilophodont types. Concerning the genealogy of the
Elephants, it is observed that the presence of simple tetraconodon$
premolars in some Mastodons suggests their descent from some
ungulate with teeth of this type, in which premolars were as fully
developed as molars; and that it is merely necessary to assume
the addition of an extra pair of columns in each of the true
molars of the Bunodont Artiodactyla to produce a dentition analo-
gous to that of the simple-toothed Mastodons. A variety of Mas-
todon angustidens named M. paleindicus is described from teeth.
It has a tendency to a rather more complex structure of the molars
than is usual in the European type, and there is a greater curvature
of the borders of the crown in the third molar of the lower jaw,
both these characters approximating towards MW. pandionis, with
which it is associated in the extreme western border of India.
Further descriptions are given of teeth of Mastodon pandionis, which
is also closely allied to Mastodon angustidens, though the structure
of the molars is more complex and the cement of the teeth is deve-
loped. It appears to have survived to a later epoch than WM.
angustidens, being found in the Upper Siwaliks.
68 Bibliographical Notices.
The third type of this group is the new species Trilophodon
Falconeri. The tooth differs from those of M. pandionis in its smooth
enamel, low vertical ridges, wide transverse valley, and trefoil-
shaped dentine islets.
Part 2 opens with a statement of the author’s conviction that
the Indian species of Dinotherium must be maintained, and are not
to be identified with the European type.
Dr. Falconer’s divisions of the genus Hippopotamus, named Hexa-
protodon and Tetraprotodon, are here united, and Leidy’s genus Che-
ropsis is included with them in the genus Hippopotamus. Some
account is given of crania of Hippopotamus sivalensis, in which the
molar teeth vary in proportions ; and the author finds that a large
series of vertebre and limb-bones show distinctions from Hippopo-
tamus amphibius. The spinous process of the axis is higher, the odon-
toid process blunter; the scapula has its long diameter shorter ;
the femur apparently includes two types; the astragalus is longer
than in H. amphibius and approximates to the pigs.
A small hippopotamus from Burma, named by Falconer and
Cautley Heaaprotodon wravaticus, is distinguished from H. sivalensis
by the shorter symphysis and the greatly diminished interval be-
tween the canines, in which characters it makes a nearer approach
to the pigs than any other hippopotamus. The species H. nama-
dicus was referred to by Falconer as larger than H. amphibius or
H. swwalensis. It has only been obtained from the Narbadas, and
the author observes that the crania referred by Falconer to H. pale-
indicus might with equal reason be referred to H. namadicus, and
describes a mandible. H. paleindicus presents a singular type of
mandible, the jaw being that of a Hevaprotodon in process of con-
version into a TYetraprotodon, the middle incisors beimg forced
inwards and greatly reduced in size by the development of the first
and thirdincisors. The H. ctravaticus is the most generalized Indian
species, and steps of successive modification are exhibited by the
species 17. swalensis, H. namadicus, and H. paleindicus, at least as
shown in the increased shortening of the symphysis of the mandible.
H. amphibius in length of symphysis rather exceeds the Narbada
hippopotamus, its inner incisors are large and the outer incisors
small; but in H. beriensis the small outer incisor has disappeared.
The representatives of swine among the Siwalik rocks are referred
to the genera Sus, Hippohyus, Sanitheriwm, and Hyotherium. An
interesting summary of modifications of the genus Sus precedes the
description of Indian species. Sus giganteus of Falconer and Cautley
is described from specimens of crania, dentition, and mandible, so as
to show its differences from S. scrofa, S. eristatus, S. barbatus. The
third and fourth premolars of this species are wider and stouter
than the corresponding teeth of most existing pigs; but the struc-
ture is similar to that of the premolars of Tetraconodon. Sus titan is
a new species founded on mandible, cranium, teeth, and limb-bones,
and is régarded as distinct from S. giganteus. The first and second
molars are of narrower and more elongated type than in that species;
but whether it is distmct from the European types may admit of
Bibliographical Notices. 69
some doubt, and it is stated that S. titan in the structure of its
lower premolars is intermediate between the mandible referred to
S. giganteus and the fossil Kuropean pigs. Another species is named
Sus Falconeri, and although the name is new it is adapted to some
well-known materials. Its cranium approximates to that of the
living S. barbatus of Borneo, though the living species has the palate
more produced behind the third molar tooth; and this fossil is well
distinguished from most of the other fossil species by the structure
of its molars, which are of complex character. In this structure it
makes an approximation to Phacochwrus, especially in its last
lower molars, which might be converted into those of Phacochwrus
if the main columns were isolated and reduced to the size of the
accessory columns. In another direction the teeth of this species
approximate to the still more complex molars of Hippohyus.. Sus
hysudricus is a fourth species, figured by Falconer, known from
ample materials, which indicate that it is distinct from living pigs in
having larger and stouter premolars, which somewhat approximate
to those of the African river-hogs, and in having the molars of the
male wider with lower crowns. ‘The last upper molars have a
conspicuously developed cingulum. A fifth species is Sus punja-
biensts, known froma mandible. It was a diminutive pig, no larger
than the existing pigmy hog of Nepaul, of which it is supposed to
be the ancestor. It was about as large as a hare.
Hippohyus sivalensis is described from the cranium and mandible,
which make some approximation to Hyotherium, though the struc-
ture of the molars is much simpler. The true molars somewhat
resemble those of Hippopotamus, but have the longitudinal and trans-
verse valleys equally developed. The molars may also be compared
with those of Hemimeryx or Hyopotamus.
Samtherium Schlagintweitt of Von Meyer is identified with the
Sus pusillus of Falconer. This genus has a well-marked cingulum
which distinguishes it from Hzppohyus, and in several respects. it
makes an approximation to Sus.
Hyotherium is another genus of Von Meyer’s hitherto somewhat
loosely identified, which the author recognizes in India. The species
H. scindiensis is known from a few molar teeth. In Hyotherium
European specimens show that the canines and lower incisors are
but little specialized.
Tetraconodon magnus is a Siwalik type only known from molars
and mandible.
Listriodon, which occurs in the Middle Miocene of Europe, is
represented by two species in the Siwaliks. It was referred to the
genus Tapirus by Falconer, and classed with the Bunodont Suina by
Lartet. The species L. pentapotamie is closely allied to the Euro-
pean form; but the second species, LZ. Theobaldi, is smaller and
distinguished by having the transverse valley wider and more open,
and by wanting oblique ridges running from the anterior and
posterior cingula to the summits of the main ridges. The memoir
concludes with a list of writings upon the fossils described.
In the third part are descriptions of a few rodents from the
70 Bibliographical Notices.
Siwalik beds. Ahizomys sivalensis is known from mandibles and a
caleaneum, and appears to be distinguished from living species by
the relative size and breadth of the molar teeth. The porcupines
are represented by a mandible named Hystrix sivalensis. Com-
parisons are made to distinguish it from H. cristata and H. hirsute-
rostris, a8 well as to show its relations with other fossil species. A
young cranium is also figured which probably belongs to the same
species. Then follow supplementary notes on ruminants. First
the Cervus latidens of a previous volume is redescribed as Oreas?
latidens, with the conclusion that the dentition indicates a large
antelope nearly equal to the eland, having marked affinity with
Oreas and less conspicuous affinity with Zragoceros and Palcoryx.
An upper molar is similarly referred with doubt to the genus Pale-
oryx. Other remains are considered to indicate the genus Bosela-
phus. Tragulus sivalensis is a Siwalik type known from its teeth,
and the author finds no difference but size to separate the fossil
-from existing species, though such slight variation as exists makes
some approach to Moschus. Moschus is a genus indicated with
doubt on the evidence of a premolar, and it is remarked that it is
impossible to distinguish this tooth from that of the musk-deer
except by its smaller size.
The genus Cervus, enlarged to include the various subgenera,
yields two new species. Cervus stmplicidens closely approaches in
tooth-characters to Cervus awis, having the necks of the crowns of
the true molars on different levels; but in the living species the
third upper premolar is relatively shorter, the outer part of the
fourth premolar rather less symmetrical, and the true molars rela-
tively wider. Cervus triplidens is nearly allied to the C. Davidi-
anus. They have strongly marked coste on their outer surfaces,
and the crowns are higher than those of Cervus simplicidens. A
third species, Cervus sivalensis, is represented by teeth resembling
those of C. Duvaucelli, but having more rugose enamel, a distinct
cingulum, and a smaller accessory column in the molar teeth.
Then succeeds a useful synopsis of the Siwalik and Narbada
Mammalia, with references to the original descriptions and to
the previous parts of the present work. Advantage is taken of
this recapitulation to vary the nomenclature of some of the types.
Part 4 is devoted to the Siwalik birds, some of which have
already been described by Mr. William Davies. Among these is the
Pelecanus Cautleyi, founded on the distal extremity of a left ulna.
Although the comparisons have shown it to be distinct from such
species as were available for comparison, the author regards the
name as provisional, since existing species remain with which no
comparison can be made.
A second species is the Pelecanus sivalensis, also founded on the
distal extremity of an ulna, and for similar reasons the name is
regarded as provisional. Phalacrocoraa 1s known from a meta-
tarsus, and is almost undistinguishable from P. carbo of New Zealand.
Leptoptilus Faleoneri is founded on yarious remains, which also
appear to the author to make the name provisional. An indeter-
Bibliographical Notices. 71
minate cervical vertebra is regarded as indicating a Siwalik stork
or allied form. The genus Mergus is quoted with doubt on the
evidence of a cervical vertebra. Struthio asiaticus was an ostrich
closely allied to the existing species, and the author doubts whether
the slight differences in their cervical vertebre can be of more than
individual or varietal value; so that this species is regarded as pro-
visional.
The Dromeus sivalensis has since been withdrawn by the author
on the ground that the bones must be referred to an Artiodactylate
mammal,
Part 5 is devoted to Mastodon teeth from Perim Island. They
comprise the first and last upper true molars of Mastodon pandionis,
and the second right upper true molar, upper milk-molars, and
penultimate lower molar of Mastodon perimensis; and having
described these teeth in detail, the author regards it as evident that
the tetralophodont M. perimensis is a more specialized form than
the trilophodont MW. pandionis. In order to convert the teeth of
the latter into the former type it is necessary that the anterior
accessory columns should be less developed, so that the valleys
would be more open. A fourth ridge should be developed in the
intermediate molars, and a fifth ridge and double talon in the last
molar. Both species have cement in the valleys. It is considered
as likely that Mastodon sivalensis is a descendant from the stock of
Mastodon pandionis, and it is thought probable that Mastodon pan-
dionis and Mastodon pentelict are both branches from the older
stock of Mastodon angustidens.
In this volume a considerable mass of material is made known
and illustrated by figures, which for the most part are excellent ;
and it is a great gain to paleontology for naturalists to be in
possession of the author’s descriptions. Admirable in many ways,
the work suffers from the disjointed manner in which the growth
of material has caused the parts to be issued; and some of the
descriptions rather convey the impression of unnecessary haste in
publishing what might perhaps have been perfected by fuller con-
sideration. There is an appearance of desiring to leave nothing
for those who may come hereafter, and yet at the same time to leave
open a way for retiring from positions which future research may
make untenable. Many of the species instituted by the author
seem to us to be founded on characters which would justify us in
extending to them the term provisional, which so often characterizes
species founded by others. Space might sometimes have been
gained which could with advantage have been taken for more ex-
tended description. Not but what the descriptions are excellent in
their way, only they could in many cases have been fuller with
advantage. The author’s strong interest is rather with what may
be termed genetic comparisons. He has done much to unravel the
affinities of species by comparing them with existing and fossil
allies ; and the speculations on descent of species are usually justi-
fied by the nature of the materials and the interest of the problems
involved. But suggestive as this pursuit of evolution undoubtedly
72 Bibliographical Notices.
is, its value is always in proportion to the degree to which evidence
has been previously elaborated by laborious descriptions and com-
parative figures. The author’s mental attitude rather disposes him
to write for those who have already written on similar subjects,
than for the many who might become students. But even in this
he has impressed his own individuality on his work in his own way,
and we take that work with much gratitude for the labour, ability,
and research which it manifests.
Memoirs of the Geological Survey of India. Paleontologia Indica,
being Fiyures and Descriptions of the Organe Remans procured
during the progress of the Geological Survey of India. Published
by order of His Excellency the Governor-General of India in
Council. Seriesiv. Vol. I. Part 4. The Labyrinthodont from
the Byort Group. By R. Lypexxer, B.A., F.G.S., F.Z.8. With
4 plates. Calcutta: Geological Survey Office. London: Tribner
& Co. 1885.
Tue Labyrinthodont which gives a title to this memoir is a new
generic type named by the author Gondwanosaurus byoriensis. The
name is taken from the geological series, Gondwana system, in
which it occurs, and the Bijori group, an upper subdivision of the
same series in the Satpura district. ‘The preservation is not all that
could be desired, the bones having disappeared from the exposed
portions of the specimen. The skull is about the size of that of the
well-known Lovomma Allmanni, and is shown to be labyrinthodont
by the structure of the teeth, a parietal foramen, the presence of
epiotic cornua, and the structure of the thoracic shield. Only in
the region of tthe epiotic bones is there a trace of external surface,
and there the ornament is closely pitted. The exoccipital region
appears to show no trace of the characteristic amphibian exoccipital
condyles, a character not without importance in determining the
classificatory position of this animal and its allies. The author
relies mainly upon the figures to convey a conception of the form,
proportions, and structure of the skull, and the relations of its
several elements. The outline was triangular, with a rounded
muzzle, the length to the breadth being as two to three. The orbits
are oval, separated by the diameter of an orbit, and are in the
posterior half of the cranium. The parietal foramen is just behind
the eyes. An oval plate, which has the aspect of a perforation in
the cranial bone, occurs on each side of the foramen. The author
regards this as a bony pedicle ; but having only the figure to judge
from, it appears to us to be an indication of minute temporal fossa,
and if so is not entirely without interest as bearing upon the affini-
ties of the group. In the pre-orbital region there is on one side a
slight depression, thought to indicate a small lyra. The nares
appear to have been near the extremity of the snout. On the
palatal aspect there is a similar absence of bony elements ; but a
Bibliographical Notices. 73
large median element is determined as parasphenoid, on each side of
which are bones that appear to be pterygoids. The vomer and
palatine are regarded as forming the arrow-head-shaped anterior
exposed part of the palate. The mandible is long, straight, and
diminishes in depth anteriorly from the condyle. An oval man-
dibular foramen is described on the middle of the under surface of
the jaw. The teeth are imperfect. One or two palato-vomerine
teeth remain, and the maxilla and dentary part of the mandible
each carry a row of small, close-set, sharp, subcylindrical teeth, which
extend back to the orbits. The dentine is simply plicated. Some
larger teeth appear to have been placed behind the palatal teeth.
The vertebral column is only known from an imperfect cast. The
notochord is represented by a large cylinder, somewhat constricted in
the middle of each centrum ; the intervertebral foramina appear from
the figure to have been exceptionally long, The author finds that
each vertebra consisted of a bony neural arch, from which a bony
plate descended on each side and joined the median ventral portion, and
he sees in this structure an analogue of the vertebrae of Archegosaurus
and Huchirosaurus. Each centrum is supposed to support parts of
two neural arches. There are impressions of fifteen ribs, which
have the usual expanded extremities and double head. The tho-
racic shield is well preserved, though the central plate is imperfect
posteriorly. It is ornamented with radiating sculpture, most deve-
loped in front. It has the usual long rhomboidal form. The lateral
plates overlap the anterior part of the median plate and terminate
posteriorly in a sharp process, beyond which another small shield is
found. The dermal scutes appear to have had the form of oats, and
were arranged in oblique rows, forming a chevron pattern, with the
angle forward, along the length of the specimen. The notochordal
character of the vertebral column, with minor ossifications in the
centrum, and the simply plicate dentine distinguish this type from
all the large labyrinthodonts except Archegosaurus ; and it differs
from that genus in the breadth of the interorbital space, development
of the epiotic cornua, in wanting a post-articular process of the
mandible, which, on the other hand, has an internal articular
buttress ; and it further differs in having the rami of the mandible
anchylosed, in having large palato-vomerine teeth, with a few man-
dibular tusks forming an inner series near the symphysis, and in
having the summits of the neural spines expanded from front to
back and transversely. The author is disposed to refer the genus
to the Archegosauride, and it is supposed to be a more specialized
type than Archegosaurvs, and of aquatic habit; its geological age
is probably Permian.
The memoir concludes with a list of writings on Labyrinthodonts
published since 1874. It is an excellent monograph, elaborated in
the author’s best manner,
Ann, & Mag. N. Hist. Ser. 5. Vol. xvi. 6
74 Miscellaneous.
MISCELLANEOUS.
A long-tongued Pteropine Bat from West Africa.
By Dr. H. A. PAcENsTECHER.
Megaloglossus Wermanni, nov. gen. et spec.
Long-tongued fruit-eating Bats have not hitherto been found
further west than the Himalayas. Our Museum (Hamburg) has
just received one through M. Soyanx, from Lsibange-Fann in
Gaboon. This great change in our zoogeographical experience justi-
fies a preliminary communication.
Our animal belongs to Dobson’s second group of the Macroglossi:
—‘ Second finger with a distinct claw ; intermaxillary bones united
in front.” It has the full dentition with 24-435 on each side.
If Melonycteris had not been separated from Macroglossus the pre-
sent species might also have been left in Macroglossus. In size and
in some of its characters it is intermediate between these two
genera ; but in other points it departs more from Macroglossus than
Melonycteris. The tail, wanting in Melonycteris, has here two
vertebre more than in Macroglossus. The membrane on the foot, ori-
ginating in Macroglossus from the fourth toe and in Melonycteris from
the third, originates here with narrow bands from the third and
second. The muzzle is still simpler than in either genus; the
second premolar, both above and below, projects beyond the others ;
two posterior palatal folds are divided, as in Melonycteris, while
they are not so in Macroglossus. As the tongue is as long as in the
much larger Melonycteris melanops, Dobs. (alboscapulatus, Ramsay),
and at the same time broad, I propose the generic name of Megalo-
glossus.
The species is dark brown, rather lighter on the body; total
length from the muzzle to the interfemoral membrane 90, of the
forearm 45, of the third finger 80 millim.
The species will be fully described and figured in the supplement
to the Annual Report on the Museum for 1885.—Zool. Anzeiger,
April 27, 1885, no. 193, p. 245.
On the Mode of Development of Cantharis vesicatoria.
By M. H. Beavreearp,
After three years of investigations I have the satisfaction of being
able to present to the Academy the solution of a question which has
hitherto remained a mystery. It has been attempted in vain to
ascertain where Cantharis vesicatoria was developed, and whence
came those dense masses of insects which annually settle upon the
ash trees and completely strip them of their leaves.
When, in the course of the investigation that I have undertaken
upon the tribe Vesicantia, I came to the question of the develop-
ment of the Cantharis, M. Lichtenstein, of Montpellier, had succeeded
by artificial rearing in demonstrating that the Cantharis passes
through the various stages of hypermetamorphosis, and that its larvee
live upon honey. As he had only published very succinct descrip-
tions, unaccompanied by figures, of the various states of the insect, I
Miscellaneous. 75
was obliged to repeat these artificial breedings for myself. My
experiments succeeded.
I then made excavations with the purpose of collecting the pseudo-
chrysalis, the form under which the Cantharis winters. I soon found
pseudochrysalides very like those of which | was in search, but which,
on exclusion, furnished me with Cerocoma Schreberi, a vesicant beetle,
the mode of development of which was also unknown. I had the
honour to communicate these results to the Academy at its meeting
of 21st July, 1884.
At the end of that year, in the beginning of December, I was
enabled by the liberality of the Municipal Council to undertake
another journey into the departments of Vaucluse and Gard. I
returned to Aramon, when J had found the Cerocoma. I was
attracted to that place by the exceptional abundance of the Cantha-
rides. ‘This locality is near Avignon, Some sandhills, which were
worked some years ago and then abandoned, are frequented by
numerous Hymenoptera, and form an excellent investigation-ground.
In the same mound in which I had found the Cerocoma, I col-
lected, at a depth of more than 1 metre in the wall, some pseudo-
chrysalides of large size and of a pale-straw colour, which I noticed
in my book of observations as resembling in their various characters
those which I had obtained in my artificial rearings. These pseudo-
chrysalides were found in the midst of an innumerable quantity of
cells of a Hymenopteron which 1 was able to determine, Colletes
signata, and in the vicinity of cells of three or four times the size of
another species of Colletes, the exclusion of which I have not yet
obtained.
On my return to Paris with my booty I had the mortification to
see a certain number of my pseudochrysalides gradually wither
away, so that in the month of May I had only two left in good con-
dition. At this period no appreciable change had taken place, when,
on the 12th May, the integument of one of my pseudochrysalides
split upon the back, and I saw issue from it a larva (the third larva
of the Vesicantia), which, after three or four days of activity, fell
into complete torpor. On the 26th May my larva changed into a
pupa, and I could then, from the characters of the antenne, head,
and prothorax, assure myself that this time I was not in presence
of the Cerocoma, and my anxiety became extreme. I compared it
with the pups of Cantharides which I had artificially reared and
preserved; there seemed to me to be no difference between the two
forms. The following are the successive modifications that I ob-
served.
The eyes acquire a brown and then a black tint; by degrees the
mandibles become coloured ; a very slight iridescent tint appears
upon the head and then upon the prothorax. On the 5th of June
the forehead and the articulations of the legs were coloured brown.
The high temperature of the last few days assisting. the transforma-
tion was soon complete; the iridescent coloration gave place toa
brown tinge and then to green, and I found myself in presence of a
Cantharis. The individual is a male.
To sum up, I found the Cantharis in the midst of the cells of
76 Miscellaneous.
various Colletes; it lives, therefore, in the larval state at the
expense of those Hymenoptera.
Several reflexions deserve to be recorded here upon this matter :—
1. The pseudochrysalides, which I found in considerable numbers,
were not enclosed in the cells of the Hymenoptera, but lay in their
vicinity, in the sand. My rearings give me the reason of this fact,
—I have always found (and M. Lichtenstein had also pointed this
out) that the second larva of the Cantharis, after exhausting its
provision of honey, buried itself in the soil, to become converted
there into the pseudochrysalis. Things go on in nature as in my
experimental tubes, and I find the pseudochrysalis among the sand,
ata greater or less distance from the cell in which the larva lived
as a parasite. This is a distinctive peculiarity which also belongs to
the Cerocoma, and constitutes an important differential character
with regard to the mode of development of Svtaris and Stenoria.
The latter remain to the close of their evolution within the cells of
which they have taken possession, and it is in these cells that we
find these pseudochrysalides. The larvee of Cantharis, like those of
Cerocoma, are sufficiently powerfully armed to explain easily how,
after having exhausted the provision of honey, they succeed in
perforating the very thin wall of the cells of the Colletes in order to
bury themselves in the sand.
2. I think I may repeat with regard to Cantharis what I said of
Cerocoma. I have found the pseudochrysalis of Cantharis in the
midst of the cells of Colletes, but I do not think that these Hyme-
noptera are the only ones capable of nourishing the parasitic larve.
The various subterraneous Hymenoptera which provide their larve
with a pasty honey may be indifferently the hosts of these parasites,
and in proof of this I have the artificial rearmgs. M. Lichtenstein
succeeded in rearing the larve of Cantharis by feeding them on the
honey of Ceratina. I have also succeeded by means of the honey
of Megachile and that of Osmia tridentata.
3. It seems probable, considering the comparatively small size of
the cells of Colletes signata, that, in order to arrive at its full deve-
lopment, the Cantharis must consume the honey of several cells. It
is easy to understand that this may be the case when one knows
the voracity with which the larve of this insect devour honey and
the activity that they display.
In conclusion, I shall record an experiment that I have made for
the purpose of destroying once for all the idea put forward by
Neutwich, who asserts that the vesicating power of the Cantharides
is only developed after copulation. I have already shown that the
cantharidine has its chief locality in the generative organs; and I
have taken advantage of an opportunity that occurred to me of
studying the action of those organs, with perfect certainty that there
had been no copulation, since the insect had attained the perfect
state under my own eyes. I therefore removed the generative
organs from the insect on the 7th June at 11 o’clock in the morning,
and applied them immediately upon my forearm after the method
which I have already indicated. At 5 o’clock in the evening the
apparatus was removed, and a considerable vesicle was soon deve-
loped. This experiment can leave no doubt as to the error committed
by Neutwich.—Comptes Rendus, June 8, 1885, p. 1472.
UT S OF NU MBER. 91.—Fifth Series.
ec Page
“ihe a. On some Deep-sea and Shallow-water Hydrozoa. By Joun J.
Be, Quztcn, B.Sc. (Lond.), Natural History Museum. (Plates1.& II). 1
Pia IL. N otes to the Australian Sponges recently described by H. J.
Carter, F.R.S. By Dr. R. v. Lenpenrerp, in Sydney ............ 20
A III. On the Leredo utriculus of Gmelin, with Remarks upon other
Sinip- worms. By SYLVANUS Ean BES Oo cc dies: Sala genial g 25
a Pr,
ay .
IY. Report on the Testaceous Mollusca obtained during a
Dredging-excursion in the Gulf of Suez in the Months of February
and March 1869. By Roszrr MacAnprew.—Republished, with
Additions and Corrections, by Atrrep Hanps Cooxn, M.A., Curator
in Zoology, Museum of Zooloey and Comparative Anatomy, Cam-
a a
at = eee
SS
; ree ra Me Ny ssc ena iatr alk: Mavs oy yiaiedele ree ielnt coa'e baie Sage x= 32
— -Y. On Doratopteryx of Rogenhofer, a Genus of Moths allied to
os Himantopterus. By Arruvur G. Burren, A Lids EGA ag WOT eek shes t 51
| YI. On the Blue-belted Species of Butterfly-genus Prothoé.
: By Agraur G. SLL Tivo hehe G5) By aa OY Abt ted Ce eagle aT eRe IR STEER 52
| VII. N otes on Mesozoic Cockroaches, | By Samvret H.Scupprr .. 54
| BIBLIOGRAPHICAL NOTICES.
: | - Tho Birds fi Lancashire. By F.S. Mrrowett .............0.... 65
_ Memoirs of the Geological Survey of India, Pabsoatolons Indica,
being Figures and Descriptions of the Organic Remains procured
during the Progress of the Geological Survey of India. Series x.
Indian Tertiary and Post-Tertiary Vertebrata. — Vol. ILI.
Parts \—5. . By Kp Lyprxxer, BAL, E.G:S. F.Z8.0 2. 2. O6
Memoirs of the Geological Survey of India. Palezontologia Indica,
being Figures and Descriptions of the Organic Remains procured
during the Progress of the Geological Survey of India. Series iv.
Vol. I. Part 4, The Labyrinthodont from the Biori Group.
By fe Eavericen, BA) Gee ES ecient ec ien vine pei
MISCELLANEOUS.
“A long-tongued Pteropine Bat from West Africa. By Dr. H. A.
PAGENSTECHER .......... Deaptee emree are cee Gals) ener nis won aio 14
On the Mode of lyn of Cantharis vesicatoria. By M. H.
MSE PL AOSIS oon ig is Aisa pMe Ma eN aH et waite IGA A aka w/o ease «oa 4b.
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VIIL.—Remarks on the Geographical Distribution of the
Lacertilia. By G. A. BOULENGER.
In the present article I do not intend to give a detailed account
of the geographical distribution of Lizards—a work which
has to be postponed until the revision of all the genera and
species is completed. But, general as these notes are, they
will, I trust, be sufficient to establish an important fact, viz.
the very great difference between the geographical distribu-
tion of Lizards and that of other groups of reptiles, and
especially of the Batrachians, of whose distribution I have
lately* treated.
The accounts hitherto given of the geographical distribu-
tion of reptiles were founded upon material chiefly derived
from the works of Duméril and Bibron and of Gray. It has
already been pointed out how artificial many of the syste-
matic groups adopted by these authors are, and I have
recently endeavoured to replace them by a more natural
arrangement. No one will deny that a classification based
on osteological as well as external characters must lead to a
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* Cat. Batr, Grad. &e. p. 105.
Ann. & Mag. N. Hist. Ser. 5. Vol, xvi. rf
78 Mr. G. A. Boulenger on the Geographical
If we attempt to divide the globe as to its Batrachian
fauna, two primary divisions present themselves, viz. a
northern zone, comprising the Paleearctic and Nearctic Regions,
and an equatorial southern zone. But for Lizards we have
to draw a line from pole to pole, forming the Old World
and Australia on the one hand, and America on the other,
into primary divisions. And, proceeding to further sub-
division, we find that the Hthiopian and Oriental or Indian
Regions, which in their Batrachians are so closely related, have
little in common as regards Lizards; whilst, on the contrary,
the Oriental and Australian, so widely different in their
Batrachians, are extremely similar. We find also that the
Palearctic or Kuropxo-Asiatic, the Batrachian fauna of which
is so well characterized and without any affinity whatever to
the Ethiopian, bears the closest resemblance to the latter
region, differmg only in the absence of various types which
flourish in the tropical and subtropical zones. However,
before proceeding to further remarks as to this division, I
must give a synopsis of the ranges of the various families
into which I have divided the order Lacertilia.
The two families Geckonide and Scincide may be left out,
as, being composed of a very large number of genera which
are distributed over the whole of the warmer parts of the
world, they may be termed cosmopolitan. We must notice,
however, that they both agree in being scantily represented
in South America and abundantly in Australia. Dismissing
also the small family Kublepharide, the extraordinary distri-
bution of which (West Africa, Southern Asia from the
Euphrates to Bengal, and Central America) is unparalleled,
we retain the following families, which, owing to their more
restricted range, throw greater light upon the subject. They
may be divided into two groups: A. Small families, having a
narrow range; B. Large and more widely distributed fami-
lies :—
A. Uroplatide. Madagascar.
Pygopodide. Australia.
Xenosauride. Central America.
Zonuride. South Africa and Madagascar.
Aniellide. California.
Helodermatide. Mexico.
Xantusiide. California, Central America, and Cuba.
Gerrhosauride. Africa and Madagascar.
Anelytropide. Africa.
Dibamide. New Guinea.
B. Agamide. Most abundantly represented in the Hast
Indies, less so in Australia, still less in Africa and
Distribution of the Lacertilia. 79
Asia north of the Himalayas. Absent from Mada-
gascar and New Zealand. Bs
Iguanide. America. Two genera in Madagascar, and
another in the Fiji Islands.
Anguide. The bulk of this family occupies Central
America and the West Indies, spreading to North
and South America. One genus (Anguis) in Europe
and the Mediterranean district, another (Pseudopus)
represented by one species in the Mediterranean dis-
trict and one in the Khasia Hills.
Varanide. Africa (excl. Madagascar), Oriental Region
to Asia Minor, Australia.
Teiide. America.
Amphisbenide. Tropical and subtrepical America,
Africa (excl. Madagascar), and the Mediterranean
district.
Lacertide. Africa (excl. Madagascar), Europe, Asia,
few in the East Indies.
Chameleontide. Africa, most abundant in Madagascar,
one species, identical with a North African, extending
to India and Ceylon.
Passing now to an examination of the relationships be-
tween the various parts of the globe as to their Lizard-faunas
we must first establish the two great primary divisions which
have been alluded to above, and which, in accordance with
Mr. Sclater’s nomenclature*, I will term the Neogean and
Paleogean Realms. ‘The former is characterized by the pre-
sence of the Iguanide, Teiide, and abundance of Anguide ;
the latter by Agamidez, Varanide, Lacertide, and Chame-
leontide. ‘This division is the more natural, as we find in
both realms, within their respective families, a repetition of
the same forms having adapted themselves to similar condi-
tions. Few more striking examples of parallel series of forms
can be found than the families Agamide and Iguanide, o1
the Lacertide and Teiide. Such parallel series occur in
almost every division of the animal kingdom: among the
Batrachia we have the Arcifera and the Firmisternia; among
the Chelonia the Cryptodira and the Pleurodira; and there
can be no doubt that the indications furnished by the range
of such analogous large groups are of the greatest importance
in tracing the relationships of the faunas of the various parts
of the world.
The Neogean Realm may, in this summary review, be
described in few words. Its fauna is very uniform as
* Journ. Linn. Soc. ii. 1857, p. 130.
7*
80 Mr. G. A. Boulenger on the Geographical
regards groups of higher rank, and the changes from the centre
towards the North and South are very gradual. And it is note-
worthy that the Central-American fauna (of which the North-
American is but an offshoot) presents a greater variety of
types than South America; thus it possesses representatives
of every one of the eleven families which occur in the realm,
viz. Geckonide, Eublepharide, Iguanide, Xenosauride,
Anguide, Aniellide, Helodermatide, Xantusiide, Teide,
Amphisbenide, and Scincide ; whereas South America lacks
the small groups Eublepharide, Xenosauride, Aniellide,
Helodermatidz, and Xantusiide. As the greater abundance
and variety of forms of the Anguide occurs in the northern
half and the West Indies, and the reverse is the case as re-
gards the Teiide (especially with reference to variety of
genera) and the Amphisbenide, we may safely draw the
boundary-line between two regions or subregions, as it may
be thought fit to term them, at the Isthmus of Panama, the
West Indies being comprised with the northern region.
Lizards range only as far north as British Columbia (Ger-
rhonotus ceruleus), Minnesota (Humeces septentrionalis), and
Massachusetts (Humeces fasciatus) ; whilst they have pene-
trated to the Straits of Magellan (Liolemus magellanicus).
In the following remarks on the Paleogean Realm Wallace’s
zoo-geographical division is followed, with the view of exami-
ning how far it agrees with the facts deducible from the
distribution of the Lacertilia.
1. The Palearctic Region.—There is no more reason for
separating this region from Tropical Africa than there is for
separating North from Tropical America. Its chief character
is the abundance of Lacertide, which group is also richly
represented, by identical or closely allied genera, throughout
the continent of Africa. In the Oriental Region they disap-
pear, being eastwards represented only by the aberrant genus
Tachydromus, which is an Oriental form.
In Europe and the Mediterranean district Anguide occur,
represented by two genera, viz. Angus, which has its nearest
ally in Ophiodes of South America, and Pseudopus (of which
a second species is found in the Khasia hills), closely related
to Ophiosaurus of North America. The occurrence of these
American types is analogous to that of the Batrachian genus
Hyla in the same region, and the fact that the Khasia hills
are also the home of a distinct species of that genus is ex-
tremely remarkable ; but this is the only analogy that can be
found between the Batrachian and Lacertilian faunas of the
Palearctic Region. The Mediterranean districts of Africa and
Asia, as well as the tract extending to North-western India,
Distribution of the Lacertilia. 81
are characterized by a mingling of European and Ethiopian
forms, with, however, strong predominance of the latter—the
true Lacerte being outnumbered by such forms as Hremias,
Acanthodactylus, &c., and the families Agamide, Amphis-
beenide, and Chameleontide being represented by a greater or
less number of species. The homogeneity of the desert-fauna
which extends from North-west Africa to Sind is striking ;
not only the genera remain nearly the same, but even some of
the species are identical throughout or but slightly modified.
African forms, such as the Lacertoid genera Hremias and
Scaptetra, penetrate into Central Asia and Mongolia; the
genus Phrynocephalus, so characteristic of that district, is but
a slightly modified form of the African Agama. By the
- abundance of these types, and by the absence of the genus
Lacerta* and the Anguide, the interior of Asia differs strongly
from Europe, without showing any relationship to the Oriental
Region ; its character is essentially African. The Manchu-
rian Subregion shows a decided preponderance of Indian
forms, as is rendered especially apparent by the presence of
several species of the genera Gecko and Tachydromus, which
are otherwise restricted to the eastern parts of the Oriental
Region, extending far into the Indian archipelago, but not
ranging west of Bengal. Japan, with the widely-distributed
genus Humeces and the genera Gecko and Tachydromus, is
without any affinity whatever to the Palearctic Region—a fact
in accordance with the distribution of Ophidians, as shown
by Dr. Giinther 7, but different from that of Batrachians.
The Manchurian Subregion is therefore to be included in the
Oriental Region. The northern limit of the Lacertilia in Asia
is still to be ascertained; in Europe they are known to occur
as far as Lapland (Lacerta vivipara and Angus fragilis).
2. The Ethiopian Region.—The affinity between this and
the preceding region is so great, and the passage between the
two so gradual, that it is hardly possible to draw any satis-
factory boundary-line; should such a boundary have to be
traced, the southern limit of the Sahara appears to be the
most natural. ‘The south of the African continent exhibits by
far the most varied Lizard-fauna, no less than ten families
(viz. Geckonide, Agamide, Zonuride, Varanide, Amphis-
benidee, Lacertide, Gerrhosauride, Scincide, Anelytropide,
and Chameeleontid) being represented, the smaller of which
* A single species, Lacerta vivipara, ranges far to the east in Northern
Asia, its presence being recorded in Amoorland; how far ZL. agilis ex-
tends into Siberia is unknown at present; no other ZLacerte are known
to occur in Siberia.
+ Proc. Zool. Soc. 1858, p. 379.
82 Mr. G. A. Boulenger on the Geographical
(Zonuride, Gerrhosauride, Anelytropide) gradually disappear
towards the north. As Africa shows some points of relation
to Tropical America in certain Batrachians, such as the
Aglossa, the Cecilian genus Dermophis, so a point of similar
affinity is suggested by the Amphisbenide, of which eight
genera occur in Africa and five in America, two being
common to both regions. The distribution of the Lacertilia
does not afford any support to the divisions into the conti-
nental subregions proposed by Wallace. Madagascar is as
differentiated from continental Africa in its Lizards as in its
Batrachians, although it has less in common with the
Oriental Region; we find likewise strictly American forms
(the Iguanoid genera Hoplurus and Chalarodon) and a
striking negative feature in the absence of such families as
the Agamide, Amphisbeenide, and Varanide ; it possesses a
peculiar family—the Uroplatide. The sole pomt by which
affinity to the Oriental Region might be thought to be indi-
cated consists in the presence in the Andaman Islands of a
species of the Geckoid genus Phelsuma. But Madagascar
has important elements in common with Africa, viz. the
Chameleontide (represented by twenty-four species, nearly
half the number actually known), Gerrhosauride, and Zonu-
ride. It should therefore be regarded as a subregion of the
Ethiopian Region, having much in common with the latter,
a little with South America, scarcely anything with the Hast
Indies, and nothing with Australia.
It is remarkable that this region is relatively poor in
arboreal lizards, these being almost exclusively represented
by the Chameleons. The Agamoids, so rich in arboreal
forms in the Oriental Region, are terrestrial in Africa (Agama,
Aporoscelis, Uromastix), and so are also the few Iguanoids
of Madagascar.
Although the distribution of minor groups is beyond the
scope of this paper, the range of a few genera may be noticed, as
affording strong support to the views advocated on the rela-
tionship of the Ethiopian and Paleearctic Regions.
1. Lacerta. Three species in South Africa, four in
Tropical Africa, about twelve in Europe and the
circum-Mediterranean district.
. Tropidosaura. Two or three species in South
Atrica, three in the circum-Mediterranean district.
3. EHremias. Numerous throughout Africa and South-
western and Central Asia and Mongolia.
. Scapteira. Two or three species in South Africa,
two in Central Asia.
bo
is
Distribution of the Lacertilia. 83
5. Chalcides*. 'Ten species in Madagascar, one in
South Africa, six in the circum-Mediterranean
district.
3. The Oriental Region—We have seen above that the
Manchurian Subregion of the Palearctic Region should form
part of the Oriental. The northern boundary traced by
Wallace appears otherwise satisfactory, save that the desert
of North-western India belongs essentially to the Ethiopian
Region. This region thus defined is poor as regards the
number of families: these are the Geckonide, Hublepharide
(in India only), Agamide, Varanide, Lacertide, and Scin-
cide. We have noticed above the occurrence of Pseudopus
(Anguidz) in the Khasia hills.
It possesses also a representative of the Chameleontide in
India and Ceylon; but the fact that this unique species is
identical with a North-African one clearly shows that it must
be treated as an immigrant from the Ethiopian Region. For
the same reason we may omit such genera as Agama and
Uromastix, which occur in Northern India, and the Lacertoid
genera Ophiops and Cabrita, which are merely outposts from
the neighbouring region. The Lacertide, therefore, are
restricted to a single Oriental genus, Tachydromus. The
Geckonidz and Scincide are cosmopolitan ; the Eublepha-
ride have such a range as to throw no light on the relation-
ships of this with other regions; and, finally, the Agamide
and Varanide occur in common with the Hthiopian and
Australian Regions. The Oriental Region does not possess a
single family of its own, a fact already pointed out for the
Batrachians. The Agamoids, by the great number of genera,
most of which are adapted to arboreal life, give a special
feature to this region, especially when compared with Africa
and Australia. ‘The subdivisions into subregions proposed
by Wallace appear to agree on the whole with the distribution
ot the Lacertilia; but this is a question that can only be
elucidated by discussing the range of genera and species, and
therefore does not fall within the scope of this preliminary
note. As to the eastern limit of the Oriental Region, it is by
no means easy to decide where it should be drawn. Wallace’s
line clearly does not answer in this case, for Celebes and the
Moluccas are tenanted by a strictly Malayan lizard-fauna,
without Australian element. The latter begins to appear
in New Guinea, where the genera Draco and Calotes are
absent ; whilst the characteristic Australian family Pygopo-
* = Seps, auct. nec Laur., + Gongylus.
84 On the Geographical Distribution of the Lacertilia.
dide is represented in its southern parts; this great island
must be regarded as the debatable ground between the Aus-
tralian and Oriental Regions. But, as observed above, there
is, as regards the Lizards, no fundamental difference between
the two; they form a single great region, which may be
divided into several subregions, but not into two primary
divisions, as required for other groups of animals.
4, The Australian Region.—Only five families occur—two
cosmopolitan (Geckonidz and Scincidee), two in common with
Asia and Africa (Agamide and Varamde), and one charac-
teristic (Pygopodide). In New Guinea occurs the small
family Dibamide; and the Fiji Islands possess a genus of
Iguanoids, Brachylophus, the nearest ally of which is perhaps
the West-Indian Cyclura. The bulk of the fauna consists of
the Geckonide and Scincide. The latter,as regards number
of species and variety of forms are not surpassed or even
equalled in any other part of the world, and the former are
well represented, although less so than in the Oriental Region.
In the islands of the South Pacific, New Zealand included,
these two families only are found, but represented by nume-
rous species, some of which are types of peculiar genera,
usually showing but remote affinity to the continental forms.
The Agamoids are mostly terrestrial, some semi-arboreal
and semiaquatic. Special affinity with the Oriental Region
is shown in the genera Physignathus (four species in Aus-
tralia, two in Siam and Cochin China) and Gonyocephalus
(numerous throughout the Malayan and Papuasian islands,
two species in Queensland). One of the most remarkable
features of Australia is the small number of families, it being
in this respect inferior to Hurope, which possesses represen-
tatives of seven, a remark which applies also to the Batra-
chians, of which Australia has four families and Europe
seven.
Thus we arrive at the conclusion that the zoo-geographical
regions generally in use, and especially their degree of rela-
tionship to one another, receive little support from the study
of the distribution of Lizards ; that the distribution in zones,
which is so satisfactorily shown by the Batrachians and the
freshwater Fishes, is contrary to the plainest evidence as
regards Lizards, which at the present time range more
according to longitude; that the two great divisions originally
proposed by Mr. Sclater, and derived from the study of
passerine birds, hold good; and that, if a division of the
world had to be framed according to the lizard-faunas, the
primary divisions would be the following :—
On Reptiles and Batrachians from Brazil. 85
I. Paleogean Realm.
Two regions:—1. Occidental (= Palearctic Region, excl.
the Manchurian Subregion, + Ethiopian Region of Wal-
lace); 2. Oriental (=Oriental + Australian Regions of
Wallace).
II. Neogean Realm.
Nearctic + Neotropical Regions.
1X.—Second List of Reptiles and Batrachians from the
Province Rio Grande do Sul, Brazil, sent to the Natural-
History Museum by Dr. H. von Ihering*. By G. A.
BOULENGER.
THE following species, which were not contained in the first
list, formed part of a large collection made by Dr. von Ihering
at 8. Lorenzo, on the southern border of the Lagoa dos Patos.
As before, such species as have not been recorded from Rio
Grande do Sul by Hensel are marked with an asterisk.
REPTILIA.
CHELONIA.
*1, Hydromedusa tectifera, Cope.
- Hydromedusa Maximiliani, Wagler, 1830, nec Mikan.
Chelodina Maximiliant, Dum. & Bibr. 1835.
Hydromedusa tectifera, Cope, 1869.
Hydromedusa platanensis, Gray, 1873.
Hydromedusa Wagleri, Gunth. 1884.
Two specimens, adult male and young. In the latter, the
nuchal is in contact with the first costal, whilst in the former
it is so on one side only—a fact which justifies the view ex-
pressed in the above synonymy.
*2. Thalassochelys caretta (L.).
LACERTILIA.
ANISOLEPIS, g. n. [guanidarum.
Tympanum distinct. Body cylindrical; no dorso-nuchal
erest. Dorsal lepidosis heterogeneous, keeled; ventral scales
* Cf. Ann. & Mag. Nat. Hist. ser. 5, xy. pp. 191-196.
86 Mr. G. A. Boulenger on
large and keeled. A strong transverse gular fold; no gular
sac. Head-scales small. Digits subcylindrical, with smooth
lamellz inferiorly. No femoral pores. Tail long, round.
Lateral teeth tricuspid; no pterygoid teeth. No sternal
fontanelle. Abdominal ribs.
Allied to Enyalius, Urostrophus, and Liosaurus, which
have likewise smooth infradigital lamelle, no femoral pores,
and, like Polychrus and the Geckonidz, abdominal ribs and
no fontanelle in the sternum.
*3. Anisolepis [heringii, sp. n.
Head small, body elongate. Nostril lateral, near the end
of the snout; ear-opening moderately large, oval. Upper
head-scales small and smooth, smallest on the supraocular
region ; occipital enlarged, suboval, about as large as the
tympanum ; upper labials eight, very low. Gular scales
granular and keeled medially, larger and smooth anteriorly,
gradually larger, rhomboidal, imbricate, and strongly keeled
towards the gular fold, which is strong and straight. Median
dorsal scales larger, irregular, imbricate, strongly keeled, the
largest forming one or two indistinct longitudinal series on
each side of the vertebral line; dorso-lateral scales very small,
granular, keeled, unequal, intermixed with irregularly scat-
tered enlarged scales. Ventral scales much larger than dorsals,
equal, rhomboidal, imbricate, strongly keeled, the keels form-
ing straight longitudinal series. ‘The adpressed hind limb
reaches the axilla or the shoulder. Tail more than twice as
long as head and body, covered with equal keeled scales.
Olive-brown above, with a series of triangular dark brown
spots on each side of the vertebral line, forming a zigzag band ;
this is bordered externally with yellowish or reddish; the
triangular spots may send forth narrow dark brown lines
obliquely directed posteriorly down the sides; lower surfaces
yellowish or coppery, the throat with a few blackish dots or
longitudinal lines; tail above with a series of rhomboidal,
dark, light-edged spots.
millim.
Rotalslen othe yeccn ois. keke ae eee 245
lead Be Rectan ices See a es 15
Wadthyoreheadt-s5.9.) cr.cn ae eine tee 10
IBIOGIA Ms. Ale OI ee nea IEP esl 6c 64
IHOre simp eM a Stk en ta elena Dif
Elindglimnbgassiekcccs cobra ce ee 4]
Ube eens ie Ska ied Sea een ce oe 176
Two female specimens.
Reptiles and Batrachians from Brazil. 87
*4, Mabuya dorsivittata, Cope.
Originally described from Paraguay. Specimens from
Uruguay are also in the Natural-History Museum.
OPHIDIA.
*5, Geophis reticulatus, sp. n.
Pp » Sp
Internasals not larger than postnasals; frontal broader
than long; no preocular; two postoculars; seven upper
labials, third and fourth entering the eye; temporals 1+2.
Scales in fifteen rows. Ventrals 156; caudals 26. Pale
brownish above, each scale edged with dark brown; an ill-
defined dark brown collar; lower surfaces uniform whitish.
Head and body 315 millim.; tail 40 millim.
A single specimen.
#6. Ablabes Agassizii (Jan).
Exrenis Agassiz, Jan.
Several specimens, representing two varieties of coloration.
One is olive-grey, with the bands along the body very indi-
stinct ; the other is brown on the sides, with a whitish black-
edged streak on each side of the back, which is brick-red
between them. A specimen from Uruguay in the museum
agrees perfectly with Jan’s figure.
7. Tomodon dorsatus, D. & B.
8. Herpetodryas carinatus (L.).
*9. Leptognathus ventrimaculatus, sp. n.
Habit moderately slender, compressed. JInternasals not
half the size of the prefrontals; frontal as broad as long,
about two thirds as long as the parietals; nasal undivided ;
loreal not twice as long as high, largely entering the eye; a
small preocular may be present above the latter shield; two
postoculars, upper largest; six upper labials, fifth largest,
third and fourth entering the eye; lower labials eight, five
anterior in contact with chin-shields ; temporals1+2. Scales
smooth, in fifteen rows, the vertebral enlarged, hexagonal.
Ventrals 156 or 161; caudals 45 or 48. Body with blackish-
brown, large, transverse spots, or with two alternating series
of such spots, separated by narrow pale brownish or whitish
intervals ; head blackish brown, veined with brownish white ;
88 Prof. P. M. Duncan on the
lower surfaces whitish, largely spotted with black. Head
and body 360 millim. ; tail 90 millim.
T'wo specimens.
10. Bothrops alternatus, D. & B.
Bothrops atrox, Hensel (part. ?).
*11. Bothrops biporus, Cope.
BATRACHIA.
*1. Paludicola fuscomaculata (Steind.).
*2. Limnomedusa macroglossa (D. & B.).
*3. Phyllomedusa Lheringii, sp. n.
Very closely allied to P. Burmeistert, but the head is
smaller, not wider than the body, the snout less obliquely
truncate, and the parotoids are scarcely prominent. The
coloration is also different. Upper surfaces, the digital disks
included, green; concealed parts of the body and limbs
bright orange, with dark purple lines forming vertical bars or
a wide-meshed network ; a more or less distinct whitish line
round the lower jaw and along the outer side of forearm and
hand and tarsus and foot; lower surfaces pale yellowish, or
grey spotted with yellowish. Male with an internal subgular
vocal sac and blackish rugosities on the thumb. From snout
to vent 67 millim.
Numerous specimens.
X.—On the “Tag” of Ceelopleurus Maillardi, Mich.
By Prof. P. Martin Duncan, F.R.S.
THE “tag” of an Urchin is that comparatively bare space
on the test which is situated above, that is aborally to, the
branchial slit or “cut.”
It is a small, elongate, narrow space just on the edges of
an interradium and an ambulacrum, and the ambulacro-inter-
radial suture usuallyruns down it. As thereareten slits or cuts,
there may be as many “tags.” ‘The structure is by no means
universal, and there are groups of genera in which it does
not exist. Mr. Percy Sladen and myself found the tag well
‘“* Tag” of Coelopleurus Maillardi. 89
developed in the fossil Celopleurt of the Tertiaries of Western
India (Pal. Indica, ser. xiv., “ Fossil Echinoidea of Sind’) ;
and in investigating the morphology of the recent Celopleurus
Maillardi I found evidences of the function of the region. I
have not had an opportunity of examining the structures
upon any other recent form, and possibly the description now
given may stimulate other students of the Echinoidea to add
to our knowledge.
Dr. Giinther was so good as to allow me to study one of
the specimens of (. Mazllardi in the British Museum, and
the preparation which forms the subject of this short descrip-
tion will shortly be in the possession of the museum. A
portion of the test around the peristome was cut away, so as
to include a branchial cut and a tag, and the peristomial
membrane which is attached to the edges of the test was
carefully separated. ‘The piece of test was then placed in
nearly absolute alcohol. After the lapse of a few days the
tissue on the tag, which was in organic contact with the
test beneath, was separated, floated off, and stained with
eosin, cleared in oil of cloves, and mounted in balsam.
The base of the structure is a reticulate, perforate, and
more or less broadly spiculate calcareous layer or layers, and
the nucleated soft structures environ the hard parts. The
surface consists of connective tissue, minute nucleated cells
showing evidences of cilia, and extremely fine nerve-filaments.
In three places this common ectodermal structure became thick
and rose into three small bodies, each of which has a broad
base and a surface of digitiform and sometimes ragged pro-
cesses. The surface of each of the bodies is highly nucleated,
but no trace exists of a central canal, and, indeed, the appear-
ance given is that of solidity.
The three bunches of tissue are eminently branchial in
their appearance, and, so far as I know, resemble in their
construction the branchie on the peristomial membrane. Un-
fortunately these last structures in Coloplewrus are so covered
with pigment bodies—which are not quite absent, moreover,
from the bodies on the tags—that a satisfactory preparation of
them has yet to be made.
There does not appear to be any connexion between the
bodies on the tag and the water-system of the ambulacra, and
probably they act as respiratory organs by increasing the
surface of the common derm.
90 Mr. W. Marshall on the
XI.—Remarks on the Celenterate Nature of the Sponges.
By WILLIAM MARSsHALL*.
On different occasions I have given expression to my con-
viction that the Sponges are Ccelenterata—a conviction
which I share with Leuckart, Hickel, Von Lendenfeld, and
others. It originates from a series of morphological and
ontogenetic facts, of which radial symmetry is not the least
important. I have formulated my opinion about as follows :
—that the Sponges are Coelenterata, in which, in consequence
of the (phylogenetically speaking) very early occurrence of
sessility, profound retrogressions had taken place, induced
especially by a colossal overgrowth of the mesoderm.
Quite recently treatises have appeared from two sources on
the systematic position of the Sponges. One of them (which
certainly completely ignores my conception and its results)
argues against the Sponges belonging to the Coelenterata, and
indeed to the Metazoa at all; while the other arrives at the
result that, if the Sponges and Ceelenterata did possess com-
mon ancestors, the former must have branched off from the
latter at a time when true typical Coelenterate characters had
not yet been acquired. As both treatises have distinguished
spongiologists for their authors they call for the greatest con-
sideration ; and this the more, because they diverge so widely
from each other in the result of their deductions. One of these
memoirs is the work of F. E. Schulze}, the other of W. J.
Sollast; and although the former appeared somewhat later
than the second, we shall here discuss it first, as its treatment
of the subject is more general.
Schulze subjects the two opposite opinions—according to
one of which the Sponges are colonies of Protozoa (Choano-
flagellata), and according to the other Ceelenterata—to a
thorough criticism.
Following the lead of James Clark and Carter, Savile
Kent especially, with whom Biitschli has also recently asso-
ciated himself, had taken it upon himself, on the foundation of
observations partly correct, but partly also quite erroneous
to demonstrate the Protozoan nature of the Sponges, in which
he laid particular stress upon the nature of the flagellate cells
and the processes of development. The flagellate cells, when
* Translated from an advance copy, communicated by Dr. G. J. Hinde,
F.GS., of the paper in the ‘ Jenaische Zeitschrift,’ Band xviii. pp. 868—
880.
+ Sitzungsb. Berl. Akad. d. Wiss. 1885, pp. 179-191; translated in
Ann. & Mag. Nat. Hist. ser. 5, vol. xv. pp. 865-3877 (May 1885).
¢ Quart. Journ, Microsc. Sci. n. ser. vol. xxiv. pp. 603-621,
Celenterate Nature of the Sponges. 91
fully developed, have, like the Choanoflagellata, a peculiarly
differentiated frill (collar), which surrounds the basal part of
the flagellum like a funnel, and also pulsating vacuoles in the
interior. According to Kent the ciliated cells of the free-
swimming larve also show the same characters; but this
unfortunately has been seen by no one but himself.
Schulze, indeed, admits that it would seem hardly natural
to suppose that so peculiar a structure as the collar of the
flagellate cells had originated spontaneously twice in different
groups of animals; but that it is to be regarded as inherited by
the more complex, and therefore probably more recently diffe-
rentiated form, from the simpler and therefore probably older
form; but upon the whole he finds that, even if we leave out of
consideration a series of differences, which certainly exist be-
tween the Choanoflagellata and flagellate cells of Sponges, it
would not be a justifiableconclusion to deduce from a similarity,
however close, of unicellular Protozoa with certain cells of the
trilamellate Sponges, that the latter pertained to the former.
Moreover, in reality, in the blastula of the Sponges flagellate
cells of this kind, furnished with collars, are always deficient,
although their presence there might justly be expected, if
they originated from the Choanoflagellata. After taking the
trouble to examine how Savile Kent could have come to the
erroneous assumption of the presence of the collar in the
ciliated cells of the sponge-larve, Schulze arrives at the con-
clusion that the Sponges are true Metazoa, for they have
sexual reproduction, and in their larve two different cell-
layers, an outer and an inner one, may be clearly distinguished.
Schulze then discusses the hypothesis of the Ccelenterate
nature of the Sponges. ‘To the radiate structure occurring
occasionally in larvae and also in adults he ascribes no great
importance ; the Ascones never formed radial diverticula of
their central cavity, and if these were produced in Sycones as
sacciform distensions of the body-wall, it must be borne in mind
that the Sycones before they formed the radial tubes possessed
ontogenetically the pure type of the Ascones, so that the latter
must consequently be regarded as ancestors of the former.
Hence it seems very probable that the most ancient sponge-
forms possessed an Olynthus-like form without radial diver-
ticula of the central cavity ; and the developmental history of
the Sponges, so far as we are yet acquainted with it, presents
no sufficient ground to justify the assumption put forward by
me of common ancestors of the Sponges and Cnidaria, with
radially arranged mesenterial pouches, tentacles with urti-
cating capsules and indifferent aquiferous pores. It may be
true that the difference between the free-swimming larvae of
‘92 Mr. W. Marshall on the
the Sponges, on the one hand, and the Cnidaria, on the other,
is, on the whole, not more important than that between the
various Sponge-larvee among themselves. But as the funda-
mental differences in the structure of the two groups only
showed themselves after the metamorphosis, we are justified
in the assumption that the divergence of the two lines did not
begin before that phylogenetic developmental stage which
represents the ciliated larva on the point of metamorphosis. |
Sollas takes quite a different standpoint, as strikes one at
once on reading the proposition that he places at the head of ~
his argument, namely, that it is difficult to suppose that such
complicated structures as the collared flagellate cells of the
Sponges could so closely resemble the Choanoflagellata, and
at the same time be of independent origin. He explains the
metazoic character of the Sponges, using Lankester’s term, as
“ homoplastic,”’ and their Infusorian character as phylogenetic,
z. e. he believes the latter to be inherited, the former newly
acquired. He proceeds :—Only two characters of the Sponges
are essentially of metazoic nature, namely, the presence of both
kinds of sexual reproductive bodies and of a gastrula. As
regards the former, we find also in plants two kinds of sexual
products, and what plants and animals could have formed inde-
pendently of each other Sponges and Ccelenterata might also
have acquired independently. In opposition to the second
character, the formation of the gastrula, it is to be remarked,
in the first place, that the flagellate cells of the habit of the
Choanoflagellata occur very early in the ontogeny of the
Sponges, at least before the formation of this gastrula, as is
clearly the case in the amphiblastula of Sycon raphanus.
Secondly folding, and therefore the formation of a gastrula, is
one of the most frequent of all processes in the different develop-
mental processes of animals, and is probably easily explicable
by asimple mechanical process. So much, at least, is certain,
that foldings in numerous cases originate quite similarly and
independently of inheritance, and may lead to the foundation
of organs which may indeed be “‘ homoplastic,” but certainly
not homologous. Further, we see that the formation of a
gastrula in Sponges, as also in Cnidaria, may take place in
two ways, namely, by invagination and by cleavage of the
mesenchyma, and one or other of these two modes at least
cannot be explained by inheritance. Once more asserting
the early occurrence of the cells like Choanoflagellata in the
sponge-larvee, Sollas comes to the conclusion that the Sponges
may have developed themselves independently as a special
phylum from the Choanoflagellata, and he proposes to separate
them from the Mefazoa under the name of “ Parazoa.”
Celenterate Nature of the Sponges. 93
Moreover, the gastrula of these Parazoa differs sufficiently
from that of the Metazoa in the fact that in it the hypoblast
(endoderm) consists of cells provided with collars.
This is essentially the course of Sollas’s argumentation. It
will be seen from it that he lays thechief stress upon the presence
of the cells furnished with collars in the sponge-larve, and
according to him they occur particularly in the amphiblastula
of Sycon raphanus. I do not know whether Sollas has him-
self observed these collars in this case; except Kent, as
already mentioned, no mortal has yet seen them ; and so com-
petent a judge as Schulze says * :—“ In my investigations of
the swarm-larve of Sycandra raphanus, which can hardly
differ essentially in the structure of its larve from Sycandra
compressa, and of many other sponge-larve, I have endea-
voured, always in vain, to discover anything like the collar at
the free extremity of the cylindrical flagellate cells.” And
he then shows very plausibly in what manner Kent’s mistake
may have originated.
My observations, which appear to agree with those of most
other investigators, have shown me that flagellate cells always
make their appearance in the canal-system of the Sponges only
when a current of water through the body of the animal is
possible, 7. e. after the appearance of a gastro-vascular system
with a double communication outwards. The flagellate cells
are nothing but specially differentiated endodermic cells,
which originally have exactly the same appearance as all the
rest. This differentiation is due to division of labour: while
the flat endodermic cells chiefly effect the inception of nourish-
ment, the flagellate cells, by means of their flagella, produce
an energetic circulation of water through the bedy of the
sponge, and, chiefly by means of their collar, effect respiration. .
As im an Infusorian, an egg-cell, &c., the clear respiratory
plasma + collects as much as possible superficially, and turned
towards the point of access of the oxygen, so also in the
flagellate cells of the Sponges, both in those of the swimming-
larvee and in those of the flagellate chambers. But while in
the former the surface is more than sufficient for the reception
of a sufficient quantity of oxygen, in the flagellate cells the
case is different. They are therefore compelled to enlarge
their respiratory surface. But where can this be done? Only
where the cells come into contact with the water containing
the oxygen. ‘The rest of the body is more or less wedged in
* Loe. cit. p. 182 (Ann. & Mag. Nat. Hist. loc. cit. p. 368).
t See A. Brass, ‘ Biologische Studien, Th. I. Organisation der Thier-
ischen Zelle,’ pp. 64 and 150.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 8
94 Mr. W. Marshall on the
and enclosed between other tissue-elements; it is therefore
the upper extremity, in which the clear respiratory plasma has
collected, that is compelled to free itself from obstructive
surroundings ; the cell therefore loses its purely prismatic form
and acquires a process which is accessible to the water on all
sides. But this alone does not suffice, even if it widens
upwards ; it is compelled to enlarge its surface still more,
and this is effected by its quitting its simple cylindrical
or conical form and becoming converted into a funnel. This
does not imply, as previous observers have sometimes stated,
that the flagellate cells could not take in nourishment, but,
as we see from the other endodermic cells, for that purpose
they need not acquire a collar. Thus in my view there exists
a very essential difference between the functions of the collar
in the flagellate cells of the Sponges and in the Choanofla-
gellata, of which latter Biitschli remarks *:—“‘ There is
unanimity among observers that the collar, at least in the
Cryptomonadina, is an organ connected with the reception of
food.”
In this way I come to the conclusion that the Flagellata
and the flagellate cells of the Sponges absolutely stand in no
phylogenetic connexion, but that the two peculiarities, which
agree so remarkably, are due rather to adaptations sua generis.
The flagellate cells of the endoderm of the young sponge,
probably even in one which has originated from an amphi-
blastula, are not at once to be identified with the flagellate
cells of the larva; first of all the flagella disappear, and then
(after the cell has become flattened as an endodermic cell, and
then again extended with a fresh accumulation of the clear
respiratory plasma at the free pole), so soon as the flow of
water becomes possible, they again make their appearance
together with the collar; in the sponge-larve in which the
endoderm is formed by division of the ccenoblastema—and
these are probably the majority—there can be no question at
all of any such connexion.
While I am perfectly in agreement with Schulze in denying
any relationship between the Sponges and Choanoflagellata,
our views with regard to the degree of relationship between
the Sponges and Cnidaria are, as already remarked, very
divergent, and I will now endeavour to support and establish
my opinion in opposition even to such serious objections as
Schulze puts forward.
As we have already seen, Schulze, while placing the onto-
genetic processes in Sponges in the first line, as justly required
* Bronn’s ‘ Klassen und Ordnungen,’ Neue Bearb. Bd. 1. p. 885.
Colenterate Nature of the Sponges. 35
by modern ideas, finds no sufficient grounds, in what we at
present know of these, for ascribing, as I have done, to the
common ancestors of the Sponges and Cnidaria radially
arranged mesenterial sacs, tentacles with urticating capsules,
and indifferent aquiferous pores. In opposition to this I
might indicate that [ have not definitely assumed the exist-
ence of the tentacles and urticating capsules, but I say * :—
“ Tt may be difficult to ascertain whether the Sponges are or are
not retrogressive as regards these organs (1. e. urticating organs)
and the tentacles; but in the attempt to demonstrate the
Ceelenterate nature of the Sponges this is not of preeminent
importance ;’’ and further, “‘ In case the ancestors of the
Sponges ever possessed tentacles and urticating organs it is
not difficult to understand how these might have been lost ;”’
and, finally, ‘‘ lt is indeed not impossible that the Sponges
branched off at a developmental stage of the Colenterate stem,
at which tentacles and urticating organs had not yet been
differentiated.”
Hence there remain two points, namely the radiate structure
and the canal-system, which chiefly determine me to see
Ceelenterates in the Sponges; and it may perhaps not be
superfluous to discuss these characters here in detail.
In the first place we have to attempt to answer the ques-
tion, How did the radiate symmetry of the Ccelenterata
originate? ‘The literature that deals with this subject is not
considerable. ‘There exists, indeed, a whole series of books
and memoirs in which one would expect & priord to find state-
ments relating to it; but they refer to the radiate structure in
general, and do not enter upon its origin. Properly speaking
Leuckart f alone has spoken in various places in some detail
upon this point, and we shall therefore on the whole adopt
his guidance in what follows.
If we imagine a creature of spherical, discoidal, conical, or
cylindrical form, swimming (but entirely in the water, not at
its surface), this, supposing it to possess a body composed of
perfectly homogeneous substance, will always find itself in
equilibrium. Ii we imagine, further, that the substance of
the body does not remain homogeneous, that, for example,
a heavier part is differentiated, this will place itself either
exactly centrally, ¢.e. axially, or it must form a uniformly
developed mantle around the lighter part. Or the substance
* Zeitschr. fur wiss. Zool. Bd. xxxvii. p. 244.
+ In various places in his ‘ Jahresberichte,’ and, further, in his tract
‘Ueber die Morphol. &c. d. wirbell. Thiere, p. 14, and especially in
Bergmann and Leuckart, ‘ Anat. physiol. Uebers. d. Thierreichs,’ pp, 392
ét seqq.
S*
96 Mr. W. Marshall on the
may break up into any number of parts, and then these, if
they are not to disturb the equilibrium, must always collect
in such a manner that every plane drawn longitudinally
through the creature may divide it into two halves of equal
weight and of the same structure. If the divisional parts
are all of equal size, the mass of cells, except when it is of a
conical form, has no anterior or posterior, superior or inferior,
part founded on structure (although perhaps on movement)
(Blastula). It is otherwise, however, when the divisional
parts are of different sizes and of different weights, and are not
sufficiently numerous for one set of them to group themselves
round the other as a continuous mantle; then the larger ones,
in order to preserve the equilibrium, as also the smaller ones,
will arrange themselves in a particular manner (amphiblastula
of Sycon), and in this way special regions of the body will
orientate themselves. ‘That at the same time a eavity may
be formed by separation in the interior of the regularly con-
structed cell-aggregate, and that this may become filled with
water, is of no consequence if only the parts of the wall
remain in equilibrium. Matters remain the same if this
cavity breaks through outwards, or if a portion of the hollow
sphere becomes invaginated ; whether a swimming-gastrula
forms a central cavity by invagination or by perforation, its
mouth must be placed centrally and the parts of the wall
must arrange themselves around it and the primary stomachal
space, so that here also the equilibrium remains intact. So
soon as special organs become differentiated in our animal, even
without its acquiring a definite permanent position of the direc-
tion of movement necessitating the distinction of upper and
lower, right and left, and whether these organs are such as aid in
the taking of food (tentacles), or complications of the digestive
cavity (mesenterial sacs, gastral canals), or sexual organs, &c.
&c., the central place being already occupied by the primor-
dial stomachal space, these must always place themselves
peripherally, occur in plurality, and group themselves in such
a manner that the animal does not lose its equilibrium. In
this way the radiate structure of the primitive swimming
Ceelenterata was brought about. There is, however, another
point that must not be overlooked in these considerations. A
radiate structure is not only of great service, indeed to a
certain extent indispensable, to free-swimming creatures of
spherical or cylindrical form &c., on account of the stability
of equilibrium, but it may also be of great importance to
sessile forms, inasmuch as, acting externally, it harmoniously
increases the power of resistance in all directions; we con-
struct not only our air-balloons on the radiate type, but also
Celenterate Nature of the Sponges. 97
our towers and other fortifications. In these considerations I
have left the Echinodermata out of the question. They and
the Cnidaria are only distantly related ; the two classes have
acquired the radiate structure independently of each other,
and it shows essential differences in them. If I divide a
typical Kchinoderm (with the fundamental number five) by a
polar plane into two equal halves, so that the plane on my
side, as far as the central point, halves a radius, it will halve
an interradius on the other side of the central point; but in
typical Coelenterata (with the fundamental number four) I
shall under similar circumstances always halve similar parts.
There is no doubt that free, moving Coelenterata are more
ancient than attached ones, just as all sessile animals, which
are only conceivable in water, are descended from swimming
forms. ‘The inducement to adhesion lies in the impulse more
or less inherent in all animals to save themselves labour and
bodily exertion as much as possible, and it could only be
given when such a superfluity of food occurred that the
animals needed to take absolutely no trouble in seeking it.
When we see that the polyps, even when they are adherent,
as so many have been for a long time, have retained the
tentacles and the radiate structure, we must assume that
these are of preeminent importance; and this I believe to be
the case especially with the tentacles, which, together with the
urticating organs, play so important a part in the obtaining
of nourishment. ‘The other radiality may rather be second-
arily retained, perhaps in correlation with the tentacles (as
frequently, e. g. in Hydra, the radiate structure finds expres-
sion only in those organs) ; at least it is precisely in adherent
forms, 7. e. in those without free locomotion, that it is inter-
fered with more frequently than in others in favour of an
incipient bilateral symmetry (Fungide, Flabellum, develop-
mental stages of corals, Hydroida, &c.). In the origination
of an incipient bilateral symmetry another incident probably
cooperates, at least in part, namely regular currents of water ;
an adherent radiate animal when growing in a constant
current of water must naturally develop especially one axis,
that which lies in the direction of the constant current, for
in this way alone it offers the greatest resistance with the
smallest expenditure of force (growth-energy). A further
consequence of sessility is the possibility of an increased
development of the mesoderm, especially the formation of
heavy skeletal masses.
As soon as a change of function took place with the
gastro-vascular apparatus, as in the Sponges, as soon as the
nourishment was taken up by it, the tentacles, if they had
98 Mr. W. Marshall on the
already been differentiated at all, were lost in all cases, and
the radiate structure in most cases, and finally the mesoderm
increased in growth to such an extent that, under certain
circumstances, the stomachal space and the buccal aperture
disappeared. That the ancestors of the Sponges were not
for very long, if at all, provided with tentacles, which, indeed,
are only secondary, may be readily admitted, but they were at
least bilamellar, and at the same time, as we may conclude
from the retrogressions which continually occur, radiate ; they
had a buccal aperture and a stomachal space, from which
gastral canals ran radially to open freely outwards, breaking
through the ectoderm; and such creatures, to my mind, are
under any circumstances true Coelenterata.
When Schulze refers to the developmental processes in
Sycon, and comes to the conclusion that it is probable that
the oldest sponges possessed no radial diverticula of the gastral
space, but, like Olynthus, had a simple saccular form, we
might point out in opposition to this that in many cases onto-
geny is no absolutely true reflection of phylogeny, and that,
especially the older an animal form (as in this case the sponges
undoubtedly are), the more may the phylogenetic recapitula-
tion in the individual development be effaced. I might also
say that every true Olynthus, like a simple gastrula, is, as an
ovate, cylindrical, or conical body, radiate, for through its
polar axis we may draw an infinity of longitudinal planes,
every one-of which will divide it into two exactly similar
halves; this, however, I will not do, seeing that although it
is incontrovertibly true, it would sound something like an
evasion. But this much is certain—the radial canals and
their arrangement are not the exclusive, and perhaps not even
the oldest, criterion, of a radiate structure in the Ccelen-
terata.
If, however, we look somewhat more closely into the pro-
cesses of development, as shown, for example, in the admirable
pictorial representations that Schulze* has given us of the
ontogenetic processes in Sycon raphanus, it will not be difli-
cult to recognize a true radiate structure in certain stages. I
shall lay less stress upon the free-swimming larva with its
girdle-ring of granular cells (Taf. xvii. figs. 3-5), although
even in it a radiate structure is already expressed ; but let
the reader examine especially fig. 12 on Taf. xix., which re-
presents a young Olynthus as seen from above. We look
down upon the flattened oval extremity of a hollow cylinder,
which is perforated excentrically by a round aperture leading
* Zeitschr. f. wiss. Zool. Bd. xxxi. Taf. xyilil. & xix.
Celenterate Nature of the Sponges. 99
into the gastral space, and ‘at the periphery of the obliquely
truncated oscular area there appear symmetrically arranged
quadriradiates”’ (loc. cit. p. 288), and, indeed, six in number ;
the three rays which lie in the same plane are so placed
that the two continuous ones, which constitute a curved axis,
embrace the margin of the disk peripherally, while the un-
paired one passes perpendicular to them centripetally and
radially into the disk itself, and thus this oscular area is divided
up into six regularly radiately arranged parts (antimeres).
But if we remember what were the causes of the radiate struc-
ture it becomes clear that it is a matter of perfect indifference
what parts of the animal-body may first show it; like bila-
teral symmetry it may manifest itself in any parts which are
not situated in the central axis, and in this case one is as im-
portant as another. If the gastreea-theory be true, if of all
the systems of organs, so soon as a further division of the
animal-body occurred, the digestive cavity first developed, it
is by no means logical to assume that the radiate structure
would also have affected 7¢ first of all; perhaps quite the con-
trary may have been the case, for the gastral cavity was, in the
first place, the central and axially situated organ par excel-
lence, and it is much more probable that the displacements
and radiate arrangements of the parts in the interest of the
maintenance of the equilibrium of a swimming animal will
have first of all made their appearance in the parietal parts
situated around the stomachal cavity. And what does the
developmental history of the recent Ccelenterata teach us?
That it is of no consequence at all whether the radial arrange-
ment of the ccelenteric apparatus is brought about by centri-
fugal diverticula from the gastral space, or by partition-like
centripetally growing processes from the wall.
In my opinion the characters of the gastro-vascular appa-
ratus furnish a still stronger proof of the Ccelenterate nature
of the Sponges than the radiate structure, which only occurs
occasionally, although certainly more frequently than people
seem inclined to believe. The radiate structure may become
effaced in consequence of very long-continued sessility, just
as well as parasitism can eliminate the bilateral symmetry of
animals ; and if sessility is capable of completely suppressing
an organ so unmistakably important as a gastral cavity, it is
not easy to see why the radiate structure, which is of far less
importance to adherent animals, should be preserved under all
circumstances, or even with special frequency. But the
other Coelenterate character, the ramification of the gastral
cavity in the developed animal in the form of centrifugally
running canals opening freely outwards, is retained in a true
100 Dr. P. H. Carpenter on some Points in
sponge under all circumstances. How long these canals may
be, whether they perforate the thin wall of an Olynthus as
simple apertures, or in other forms traverse the thick body-
wall as a system of profusely branched and frequently anasto-
mosing passages, is quite irrelevant, and depends solely upon
the degree of development of the mesoderm. It might per-
haps still be objected that the canal-system of the Sponges is
developed in such different ways that it certainly cannot always
take its origin from the primitive gastral cavity, but at least
as often be formed by gaps which make their appearance
im the mesoderm, and growing on centripetally and centrifu-
gally, perforate the gastral and dermal surfaces of the sponge-
wall only in the second line. But we must not overlook one
thing: how is the gastrula of the sponge formed? In per-
fectly analogous ways: some by invagination, and with this
process the formation of the gastral canals from the stomach
outwards may be compared; the others by the appearance
first of all of a cavity in the ccenoblastema and its subsequent
breaking through outwards; and this may be placed side by
side with the origination of the canal-system from gaps occur-
ing in the mesoderm. I believe that the former process, as
well as the formation of the gastrula by invagination, is the
older and more typical, and that the second must be accounted
for by some phenomena of adaptation su generis.
In conclusion, I must again assert that it seems to me, so
far as the conditions are at present before us, that the argu-
ments which have been urged against the Ceelenterate nature
of the Sponges are far from counterbalancing those which are
in favour of it.
XII.—On some Points in the Morphology of the Echinoderms,
and more especially of the Crinoids. By P. HERBERT CAR-
PENTER, D.Sc., F.R.S., Assistant Master at Eton College.
In a recent number of the ‘Revue Scientifique’*, Professor
Edmond Perrier has published a short and semipopular
article, the title of which appears in the table of contents as
‘¢ Les Encrines Vivantes, d’aprés les Explorations du Chal-
lenger.” The author’s treatment of his subject, however, is
not altogether in accordance with the expectations to which
such a title gives rise; for his article is headed simply “ Les
encrines vivantes,” and of the six columns to which it
* Revue Scientifique, tome 35, No. 22, 80 Mai, 1885, pp. 690-693.
the Morphology of the Echinoderms. 101
extends, not more than half of one and one third of another
are concerned with a notice of the Report* on the Stalked
Crinoids dredged by the ‘ Challenger’ and the ‘ Blake.’ The
remainder of the article is almost entirely devoted to (1) an
exposition of the views which Prof. Perrier holds respecting
the circulatory apparatus of the Echinoderms in general and
of the Crinoids in particular ; (2) a new primary classification
of the Metazoa; (3) a list of the genera of recent “ Encrines”’;
and (4) a list of the species in the Paris Museum of Natural
History.
I propose to say a few words upon each of these heads,
with the exception of the second, to which I would direct the
attention of those zoologists who are interested in questions
of general classification.
Prof. Perrier regrets that with the material at my disposal
I did not enter more fully into “ une histoire anatomique des
Encrines vivantes’”’ +. At the commencement of chapter vi.
ot the ‘ Challenger’ Report, which contains 42 pages devoted
to the minute anatomy of the disc and arms, I stated expressly
that I did not propose to devote so much attention to this
subject as | had done to the comparative morphology of the
Crinoid skeleton ; for I had been “‘ able to confirm, in almost
every respect, the admirable investigations of Ludwig ft on
the minute anatomy of Antedon rosacea.” It did not appear
to me to be necessary to go into the whole question again
from the beginning, and I therefore limited myself to a
general account of the anatomy of the soft parts as far as
I have been able to work it out in six genera of Stalked
Crinoids and in three Comatule. In addition to this, I
entered into a considerable amount of anatomical detail
when discussing the generic affinities of Rhizocrinus and
Bathycrinus. But, untortunately, Professor Perrier tells us
that many of Ludwig’s results, and therefore, by implication,
of mine too, are erroneous. ‘This is doubtless only tvo true,
and J am anxiously awaiting Prof. Perrier’s promised demon-
stration of the fact.
Owing to the circumstances of the case, the material at my
disposal had not been specially prepared for minute anato-
mical work, having been in spirit for many years without any
previous hardening ; while, on the other hand, Prof. Perrier’s
observations have been carried out on a constant supply of
fresh material with all the advantages of an elaborate
* Zool. Chall. Exp. part xxxii.
+ Loe. cit. p. 693.
{ “ Beitrage zur Anatomie der Crinoideen,” Zeitschr. f. wiss. Zool.
1877, Band xxviii. pp. 255-358, Taf. xii.—xix.
102 Dr. P. H. Carpenter on some Points in
technique. Under these circumstances he has certainly seen
much which had escaped my notice. But this scarcely justifies
him in saying “Toute la physiologie des crinoides demeure
done, aprés le travail du naturaliste du Challenger, dans
Yobscurité ot il Pavait trouvée’*. I freely admit that I
have not yet risen to the conception that the water which
enters the body-cavity of a Crinoid by the ciliated funnels of
the disc is expelled by powerful muscles through pores at the
syzygies of the skeleton ; nor that the blood- and water-vessels
of a Crinoid, together with the body-cavity and its radiating
extensions, constitute a vast system of intercommunicating
canals with “le méme rédle physiologique que l’ensemble
des cavités creusées dans le corps des polypes et des
éponges ” f.
It 1s difficult to study pure physiology upon spirit speci-
mens, and it is unfortunately true that 1 have been unable to
add much to Ludwig’s account of the circulatory apparatus ;
but, all the same, / venture to think that I have made some
additions to our knowledge of the physiological anatomy of
the Crinoids. I speak under correction ; but it is certainly
my impression that the Report on the ‘ Challenger ’ Crinoids,
together with my previous writings upon the subject, contains
the first descriptions and figures of the fellowing points of
physiological anatomy :—
1. The trifascial articulation between certain joints of the
rays and arms of Bathycrinus, and the entire absence of
syzygies in this genus.
2. The complex coiling of the alimentary canal in Actino-
metra, and the accompanying variation in the structure of its
ovoid gland, to use Perrier’s own expression.
3. The presence at the sides of the ambulacra, both of dise
and arms, of radiating branches from the axial nerves of the
skeleton; and the extension of fibres from this network into
the spinelets on the dise of Pentacrinus.
4. The ramification within the stem-segments of fibres from
their central nervous axis.
5. The absence of any ambulacral grooves and of their
associated organs on the arms and disc in many specimens of
Actinometra, and on the completely plated genital pinnules
of some species of Antedon.
6. The presence of well-developed ovaries in the dise of
individuals of two species of Antedon and one of Actino-
metra t.
* Loe. cit. p. 698, + Ibid. p. 692.
{ Professor Perrier intimates that I differ from my father with respect
to that portion of the genital glands which lies within the disc of a
the Morphology of the Echinoderms. 103
The above list might be considerably extended. I trust,
however, that it is long enough to show that the Crinoid
collections made by the ‘ Challenger’ and ‘ Blake’ have not
been so completely barren of additions to our physiological
knowledge as Professor Perrier asserts.
But the absence of physiological results has not been my
only sin of omission. According to Professor Perrier, I ought
to have worked out in detail the embryogeny of the common
Antedon rosaceus of the British seas, for the purpose of throw-
ing light upon the anatomy of the adult Crinoid; and he says
that I might have obtained the necessary materials at Eton,
since he procured them at Paris *. Has he forgotten the note fT
which I sent him last year ‘On some Points in the Anatomy
of larval Comatule ”? I stated in this note that I had con-
tinually felt the want of some knowledge of the organogeny
of the Crinoid type, and had therefore procured larve of
various stages from Naples and Torquay, which had enabled
me to check some of the results obtained from an investiga-
tion of the adult anatomy. But as I was not professing to
write an exhaustive monograph of the Crinoidea, I did not
conceive it to be part of my duty to work out a detailed
account of the embryogeny ot a type which is accessible to
every European naturalist. An already lengthy report would
have been swelled to gigantic dimensions. The number of
plates required would have increased from 69 (not 61, as
quoted by Perrier) to over 100, for Prof. Perrier tells us
that his own memoir on this subject is still incomplete, and
that thirty plates are already drawn. If the various naturalists
who have undertaken to report upon the different groups of
animals collected by the ‘ Challenger’ were expected to give
a complete anatomical and physiological description of each
group, and to supplement it by a detailed account of the
embryogeny of its representative in Kuropean seas, the publi-
cation of their reports would be delayed indefinitely ; and yet
Crinoid. I can only say that I cannot understand how this impression
can have occurred to any one who has taken the trouble to ead pp. 108
and 109 of the ‘ Challenger’ Report.
* I would here express my sense of the courteous kindness of Prof. H.
de Lacaze-Duthiers, who offered to place at my disposal all the resources
of his laboratory at Roscoff, during June and July of this year, for the
purpose of working out the embryogeny of Antedon rosaceus by the most
approved modern methods. I would have given much to have been free
to accept this invitation; but my professional duties kept me in England
during both the months named, and, for the present at least, I must
leave the verification of Prof. Perrier’s results to other hands.
+ Quart. Journ. Mier. Sci. N.S. vol. xxiv. pp. 319-327 (April 1884),
104 Dr. P. H. Carpenter on some Points in
this appears to be the standard set up by Professor Perrier
for those who have large zoological collections committed to
their charge for examination and description within a limited
time.
Under these circumstances, therefore, one might expect that
the Report by Professor Perrier* upon the fifty-four species of
Asterids which were obtained by the ‘ Blake’ in the Carib-
bean Sea, a collection. second only in importance to that made
by the ‘Challenger,’ would be a model of its kind.
In the absence both of an index and of a table of contents,
one has some difficulty in making out what is contained in
this memoir of 15.0 pages. Of the ten plates which accompany
it, only one is devoted to any other part of the subject than
the external appearance of the new species established by
Prof. Perrier. At the foot of this plate, which is almost
entirely occupied by figures of pedicellarize and spines, there
is the extraordinary legend “Organisation des Hymens
discus’? ; and the reader has to turn back to the explanation
of the plates in order to learn that the name of Prof. Perrier’s
new genus is in reality Hymenodiscus. Not one of the re-
maining nine plates contains any figures illustrating the
organogeny of the starfish, a subject upon which we are still
much in want of information, despite the admirable researches
of Ludwig} upon Asterina gibbosa. Neither is there any
section of the text devoted to this question, while the amount
of physiological and anatomical information which the report
contains is meagre in the extreme.
Three years ago Professor Perrier published a short note f
in the ‘ Comptes Rendus’ to call in question the correctness
of some of Ludwig’s observations on Asterid morphology ; and
many Echinoderm students had hoped that he would take the
opportunity afforded by the material of the ‘ Blake’ Starfishes
to substantiate his charges respecting the accuracy of Ludwig’s
work on the group. But the whole question is completely
ignored, with the exception of one or two references to the
position of the stone-canal, and there is not a word about the
organogeny of the Starfish type, a subject which, according to
* “Mémoire sur les Etoiles de Mer recueillies dans la Mer des Antilles
et le Golfe du Mexique durant les Expeditions de dragage faites sous la
direction de M. Alexandre Agassiz,” Nouvelles Archives du Muséum
d’Histoire Naturelle, 2° série, tome vi. 1884, pp. 127-276, pls. 1-10
1884).
if cane oa ae Nchibhte der Asterina gibbosa, Forbes,” Zeitschr. f.
wiss. Zool. Bd. xxxvii. 1882, pp. 1-98, Taf. i.—vii.
{ Perrier and Poirier, “Sur |’Appareil circulatoire des Ktoiles de Mer,”
Comptes Rendus, t. xciv. 1882, pp. 658-660.
the Morphology of the Echinoderms. 105
Prof. Perrier’s standard for other reports, should have been
worked out in full detail.
His own report commences with a section upon the primary
divisions of the class of Stellerids, the keynote of which is
struck in the following sentence * :— On peut dire d’une
maniére générale que toutes les Htoiles de mer & tubes ambula-
eratres bisériés, ont une bouche ambulacraire, et que toutes les
Htoiles de mer & tubes ambulacraires quadrisérvés, au moins &
la base des bras, ont une bouche ambulacraire.”’
The unfortunate zoologist who is not a Starfish specialist,
but merely wishes to learn the general systematic results
which have been arrived at by the most eminent living writer
on the group, will rise from the perusal of this sentence with
an even more confused notion of the classification of the
Asterids than he had before. For, according to Viguier {,
the biserial ambulacra are usually, but not always, correlated
with an adambulacral mouth, and not with an ambulacral one
as Professor Perrier tells us.
Two pages further on he commences another section which
is devoted to the morphological signification of the pedi-
cellarizs in Asterids and Urchins and to their physiological
role. But no reference whatever is made to the elaborate
observations of Romanes and Ewart} upon the functions of
the pedicellariz ; and the discovery of glands upon the gem-
miform pedicellariz: of Kchini is attributed to Geddes and
Beddard, although these authors themselves admit § that their
“account of the structure of these pedicellariz substantially
bears out what has been said” by Sladen ||. But although
Mr. Sladen’s paper was published in 1880 it is completely
ignored by Prof. Perrier four years later; and Foettinger’s
memoir {] on the same subject is also left entirely without
notice. The same neglect of the writings of the English
naturalist who is engaged in working out the ‘ Challenger ’
* Op. cit. p. 138. :
+ “Anatomie comparée du squelette des Stellérides,’’ Arch. de Zool.
expér. et gén. t. vil. Année 1878, p. 82.
{ “ Observations on the Locomotor System of Echinodermata,” Phil.
Trans. 1881, pp. 840-852.
§ “On the Histology of the Pedicellari#, and the Muscles of Echinus
sphera,’ Trans. Roy. Soc. Ed. vol. xx. 1881, p. 392,
|| ‘On a remarkable Form of Pedicellaria and the Functions performed
thereby ; together with General Observations on the Allied Forms of this
Organ in the Echinide,” Ann. & Mag. Nat. Hist. ser. 5, vol. vi. Aug. 1880,
pp. 101-114, pls. xii., xiii.
q “Sur la Structure des Pédicellaires gemmiformes de Spherechinus
granuaris et d'autres Echinides,” Arch. de Biol. vol. ii. pp. 455-496,
pls. xxvi.—xXxviil.
106 Dr. P. H. Carpenter on some Points in
Starfishes appears in the systematic portion of Prof. Perrier’s
report.
fa the year 1882, Sladen published an account of the
structural peculiarities presented by the Pterasteride, and
pointed out their systematic value*; but although Prof.
Perrier enters into some detail respecting the structure of
Preraster caribbeus, he completely ignores all that had been
written upon the subject two years previously.
In fact, throughout the whole of Prof. Perrier’s report the
work of German and English writers upon the morphology
of the Asterids, and their relation to the Kchinodermata gene-
rally, is left entirely unnoticed. The observations of Geddes
and Beddard were made in a French laboratory and are
therefore mentioned ; but no reference is given to the place of
their publication; while the papers of Ludwig, Sladen, and
myself might never have been written so far as Prof. Perrier
is concerned. This neglect of the results of fellow workers
who do not happen to be Frenchmen may be patriotic, but it
is neither wise nor scientific; and in one case, as has been
already explained in this journal T, Prof. Perrier’s omission to
consult any one of some four papers by Pourtalés and myself
which contain descriptions of the calyx of Rhizocrinus has
led to zoological science being enriched with a new synonym.
For Prof. Perrier has at last come to the conclusion, as he
would have done at first had he taken the trouble to make
himself acquainted with the literature of his subject, that his
genus Democrinus is identical with Rhizocrenus ft.
It was pointed out by Pourtalés in 1868 §, and again in
1874 ||, that Rhizocrinus has large and well-developed basal
plates like those of Bourgueticrinus ; and in his second paper
he corrected the mistake which had been made by Sars { in
describing the basals of Rhizocrinus as internal and concealed.
These results were confirmed by myself in 1877 **, and again
* “The Asteroidea of H.M.S. ‘Challenger’ Expedition.—Part I.
Pterasteride,” Journ. Linn. Soc., Zool. vol. xvi. pp. 190, 191.
+ “Note on Democrinus Parfaiti,” Ann. & Mag. Nat. Hist. ser. 5,
vol. xi. pp. 334-336.
¢ Revue Scientifique, 30 May, 1885, p. 691, note.
§ “Contributions to the Fauna of the Gulf Stream at Great Depths,”
Bull. Mus. Comp. Zodl. vol. i. no. 7, pp. 128-180.
|| “ Zoological Results of the ‘Hassler’ Expedition,” Il. Cat. Mus.
Comp. Zool. no. viii. pp. 28, 29.
4 ‘Mémoires pour servir 4 la connaissance des Crinoides vivants,’
Christiania, 1868, p. 12.
** “On some Points in the Anatomy of Pentacrinus and Rhizocrinus,”
Journ, Anat. & Physiol. vol. xii. 1877, p. 50.
the Morphology of the Echinoderms. 107
in 1882*. I know that Prof. Perrier received copies of both
papers. In fact he quoted a portion of the second one (with-
out acknowledgment) in his brief notice of Democrinus in
the ‘Comptes Rendus’+. Nevertheless he stated in this
description that the basals of Rhzzoerinus are “ confondues,”’
while those of Democrinus are large and well developed, this
being the very character of Rhizocrinus which had been
pointed out four times by Pourtalés and myself during the
previous thirteen years.
A similar neglect of the work of other naturalists appears
in that section of the report on the ‘ Blake’ Starfishes which
is devoted to the morphological signification of the odonto-
phore. Page 159 of this section is disfigured by two serious
errors. In one place we are told that ‘les piéces radiales”’
of the young Starfish become the odontophores of the adult ;
and, as if to impress the characteristic symmetry of the Echi-
noderm type still more forcibly upon the mind of the reader,
the author continues ‘ L’une de ces pices radiales ne tarde
pas 4 présenter les sillons caractéristiques de la plaque
madreporique.”’
Much has been written by Ludwig about the morphology
of the odontophore in the Asterids; but his name, like that
of Sladen, is conspicuous by the absence of any reference to
it in the memoir of Prof. Perrier. In fact, Ludwig’s theory
that the periproct of an urchin is represented, not by the calyx
but by the ventral side of a Crinoid , is put forward as a novelty
by Prof. Perrier||, who is apparently unaware that it was pub-
lished by Ludwig so long ago as 1880, and that the morpho-
logical difficulties which it involves were pointed out by
myself in the same year {], Even in those cases when Prof.
Perrier is compelled to take account of the work of another
author, he is often unable to quote correctly, and the results are
sometimes remarkably confusing. After reproducing (with-
* “The Stalked Crinoids of the Caribbean Sea,” Bull. Mus. Comp.
Zool. vol. x. no. 4, 1882, p. 174.
+ “Sur un nouveau Crinoide fixé, le Democrinus Parfaiti, provenant
des dragages du ‘ Travailleur,’” Comptes Rendus, tome xcvi. no. 7,
pp. 450, 451.
t ‘Morphologische Studien an Echinodermen,’ Bd. i. Leipzig, 1877,
pp. 228-234, 254-269; and also “Das Mundskelet der Asterien und
Ophiuren,” Zeitschr. f. wiss. Zool. Bd. xxxii. 1879, pp. 672-688.
§ Ibid. p. 688; and also “‘ Ueber den primaren Steinkanal der Crinoi-
deen nebst vergleichend-anatomischen Bemerkungen tiber die Echino-
dermen tiberhaupt,” ibzd. Bd. xxxix. 1880, pp. 817-319.
\| Op. cit. p. 161.
q “Some disputed Points in Hchinoderm Morphology,” Quart. Journ.
Mierose. Sci. vol, xx. new ser. pp. 822-3829,
108 Dr. P. H. Carpenter on some Points in
out acknowledgement) the list of families and genera of the
living Stalked Crinoids described in the ‘ Challenger ’ Report,
he adds*, “‘ Outre ces six genres, deux autres genres d’HKn-
crines ont été décrits, le genre Jlyocrinus par Koren et
Daniellsen (sic), et le genre Democrinus par moi. Les auteurs
scandinaves s’accordent 4 penser que leur J/yocrinus n’est
qu'un Bathycrinus alarchianus mieux développé que le type.
Je trouve cependant dans les collections du ‘Talisman’
un crinoide d’assez grande taille, chez qui il existe cing
basales non soudées, presque aussi grande que les radiales;
si cet exemplaire unique n’est pas une monstruosité, c’est un
Ilyocrinus qu’on pourrait appeler [/yocrinus recuperatus.”
This paragraph contains two serious (clerical ?) errors.
The name of Danielssen and Koren’s genus is [lycrinus}, not
Llyocrinus ; and Bathycrinus Aldrichianus would be more cor-
rect than Bathycrinus alarchianus. It may be that Prof.
Perrier has had some private communication with the Scan-
dinavian authors upon the subject; but I have no knowledge
of their having published any such views as he attributes to
them. According to him they regard J/ycrinus (Carpenter?)
as a Bathycrinus Aldrichianus better developed than the type.
The type of what ? of Bathycrinus Aldrichianus? ‘This can
hardly be the case, for the two species are very nearly the
same in size, the ‘Challenger’ form from the southern seas
being, if anything, slightly larger than Bathycrinus Carpen-
tert (Llycrinus) from the North Atlantic.
Prot. Perrier’s statement reads like a paraphrase of what I
wrote respecting Bathycrinus and Ilycrinus in 1882. The
former genus was founded upon an immature specimen dredged
by the ‘Porcupine,’ which Sir Wyville Thomson named
Bathycrinus gracilis}; and I pointed out§ that “his de-
scription || of the larger species, B. Aldrichianus, from the
southern sea, seems not to have reached the Norwegian natu-
ralists before the publication of their genus J/ycrinus, which
was founded on much more developed individuals than that
dredged by the ‘ Porcupine.’”’ This B. gracilis appears to be
the poorly developed type which is referred to by Prof. Perrier
in this exposition of the views of Danielssen and Koren,
who have not, so far as I am aware, ever made any such
* ¢Revue Scientifique,’ May 30, 1885, p. 691, note.
t “Fra den Norske Nordhaysexpedition Kchinodermer,” Nyt Mag. f.
Naturvid. Bd. xxiii. 1877, p. 45.
t “On the Crinoids of the ‘Porcupine’ Deep-sea Dredging Expedi-
tion,” Proc. Roy. Soc. Edinb. vol. vii. 1869-72, p. 772.
§ Bull. Mus. Comp. Zool. vol. x. no. 4, p. 177.
|| “Notice of new Living Crinoids belonging to the Apiocrinide,”
Journ. Linn. Soc., Zool. vol. xiii. 1876, pp. 48-51.
the Morphology of the Echinoderms. 109
comparison between their [dycrinus and Bathycrinus Aldrich-
danus as 1s attributed to them by Prof. Perrier.
He further mentions a remarkable specimen with five
basals which are not united, and are almost as large as the
radials. It cannot be Zlycrinus (D. & K.), which has quite
small and very closely united basals; but if it is not a mon-_
strosity, | am quite prepared to accept it as a new genus,
Ilyocrinus, Perrier, with the specific name recuperatus. I
must protest, however, against its appearing on the same page
of Perrier’s article among the list of Crinoids in the Paris
Museum as Hyocrinus recuperatus. This is especially con-
fusing, as there is already a well-known genus Hyocrinus,
which was established by Sir Wyville Thomson in 1876.
According to Prof. Perrier’s list, the Paris Museum also
contains an undescribed species of Pentacrinus, viz. P. aste-
rius, Miller; or is it possible that this is the original Penta-
erinus which was described by Guettard, and was named
Isis asteria by Linneeus, Pentacrinus caput-meduse by Miller,
and has been finally described as Pentacrinus asterius,
Linn., sp.?
Another instance of the superficial manner in which Prof.
Perrier has examined the work which he is supposed to be
criticizing is afforded by the first line of the following state-
ment*:—“ Les Pentacrinus et Metacrinus ne diftérent d’ailleurs
que par le nombre des piéces calcaires (piéces radiales) qui
se disposent en file pour soutenir les cinq premieres paires de
bras, et peut-étre n’y avait il pas nécessité absolue de créer
pour cela deux noms de genres distincts.” The genus Meta-
crinus was suggested by Sir Wyville Thomson; but no other
generic name has been established, as hinted by Prof. Perrier,
on account of the difference of this type from that of Penta-
ertnus proper, which dates back to the time of Miller, as Prof.
Perrier knows. It is true that in my preliminary report upon
the ‘ Blake’ Crinoids T I mentioned the number of radials as
a difference between Metacrinus and Pentacrinus, because it is
the character by which the two types can be distinguished at
a glance; but I likewise stated that the radials of Metacrinus
bear pinnules, which is not the case in Pentacrinus. If Prof.
Perrier will take the trouble to refer to pp. 339 and 340 of
the ‘Challenger’ Report he will find that the two genera
also differ in the characters of the stem, cirri, arms, basals, and
disc. Nevertheless, with this statement and the figures illus-
trating it before him, he tells us that the only difference
* / Nevue Scientifique,’ May 30, 1885, p. 691.
t/ Bull. Mus. Comp. Zool, vol. x. no. 4, p. 167,
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 9
110 Dr. P. H. Carpenter on some Points in
between the two types is in the number of their radials.
What would he think of the reviewer of his Report on the
‘Blake’ Starfishes who said that the only difference between
his two genera Hymenodiscus and Anthenoides was that the
latter had but five arms and the former twelve ?
' Prof. Perrier’s investigations into the obscure and much-
neglected subject of the physiology of the Crinoids have led
him to attribute a hitherto unsuspected function to the syzy-
gial unions which occur in certain portions of the skeleton.
He tells us* :—“ Il y a au niveau de ces sortes d’articulations
immobiles qu’on appelle les syzygies, chez les Encrines, tout
un systéme de cavités puissamment munies des muscles qui
chassent évidemment l’eau dans la substance méme du tissu
imprégné de calcaire des bras ou la conduisent au dehors. et
Vexpulsent par les trous qui sont répartis 4 égale distance sur
le pourtour de la syzygie.”
It is, I think, much to be regretted that Prof. Perrier should
have departed so far from the nomenclature of Miller and
his successors as to speak of a syzygy as a kind of immovable
articulation. Miillert called it an “ unbewegliche Nathverbin-
dung ;” and he distinguished between a ‘ Nath’’ and a
“ Gelenk”’ in the anatomy of a Crinoid. He only used the
latter term when the two articulated joints were capable of
movement upon one another; and this distinction has been
almost universally adopted by later writers upon the subject,
so that the term ‘articulation immobile,” which Prof.
Perrier employs has a somewhat contradictory sound. In
the next line we are told by Prof. Perrier that among the
‘¢ Rnerines,” the term which he uses throughout the whole of
this article for the Stalked Crinoids only, the two joints are
separated by a system of cavities which open externally by a
series of pores round the edge of the syzygy. Such being
Prof. Perrier’s statement, let us examine in detail the evidence
upon which it is based. In the first place, as explained in
the ‘Challenger’ Report t, there are no syzygies at all any-
where in the arms of Bathycrinus. 'The Crinoids of this type
are consequently very far from possessing such an extensive
communication between the internal cavity and the exterior
as is supposed by Prof. Perrier’s theory that they are really
in the same physiological condition as the sponges. For the
number of ciliated water-pores on the disc of Bathycrinus
is extremely limited and by no means a “ foule d’orifices ;”
* ‘Revue Scientifique,’ May 30, 1885, p. 692, note.
+ “Ueber den Bau des Pentacrinus caput-meduse,” Abhandl. d. k.
Akad. d. Wiss. Berlin, 1843, p. 89 (of separate copy).
{ Zool. Chall. Exp. part xxxii. pp. 9, 231-2338,
the Morphology of the Echinoderms. 111
while in the case of Rhizocrinus one has still more difficulty
in accepting Prof. Perrier’s theory. For there are only five
water-pores, at any rate in R. lofotensis; and though there
are sygygies on the arms, their outlines are not marked by
anything like pores, as is the case in the Comatule. As Prof.
Perrier has plenty of Rhizocrinus-material at his command it
is a little surprising that he should have committed himself
to a general statement of this kind, which is so far from being
in accordance with the actual facts of the case. The absence
of the striz, which are so characteristic of the syzygial faces
of the Comatule, on the corresponding faces of the arm-joints
of Rhizocrinus was noted by Sars*; and without striee there
ean be no pores. ‘This observation was confirmed in the
‘Challenger’ Report; and it was also pointed out that the
closeness of the syzygial union is increased by there being a
small pit in the hypozygal which receives a backward process
on the lower surface of the epizygal?. It will puzzle Prof.
Perrier to discover, even with what his colleague Mons. Koehler
calls “ the eye of faith,” any appearance of pores round the
outline of a syzygial union in Rhizocrinus. ‘The condition of
the two living genera of the Bourgueticrinide, therefore, is
far from being such as is implied by Prof. Perrier’s very
general statement ; and he will find some difficulty in recon-
ciling it with his “ simple and new ” conception of the mode of
nutrition of the Crinoids. Let us see how far his statement is
applicable to other genera of “‘ Encrines ”’ or Stalked Crinoids.
He has never seen the arms of Hyocrinus, but apparently
takes for granted the presence of syzygial pores, such as he
believes to exist in the Comatule. 1 have not been able to
examine one of the syzygial faces in an arm-joint of this genus,
but there is no external indication of the presence of any
radiating markings such as occur in the Comatule. The lines
of syzygial union are perfectly continuous and uninterrupted,
as is well shown in the figures published by Sir Wyville
Thomson in 1876 { and reproduced in pl. vi. of the ‘ Chal-
lenger’ Report.
Here, then, is a third “ Encrine ” to which Prof. Perrier’s
statement and theory do not apply ; and he fares no better in’
the case of Holopus. If there are any syzygial unions in the
skeleton of this type at all they only occur between the two
outer radials, and it is extremely doubtful if such is the case.
At any rate, however, the apparent lines of syzygial union
have no indication of possible pores, as is the case in the
* ¢Crinoides vivants,’ p. 22.
+ Zool. Chall. Exp. part xxxii. pp. 5, 254, pl. x. figs. 1, 6, 8, 17-19.
{ Journ. Linn. Soc., Zool, vol. xvi, pp. 51, 62, ne
112 Dr. P. H. Carpenter on some Points in
Comatule. Thus, then, the only two recent “ Encrines””
to which Prof. Perrier’s very general statement is at all ap-
plicable are Pentacrinus and Metacrinus. ‘These two genera
have syzygial unions in the stem as well as in the arms;
but the apposed syzygial faces at one of the nodes of the stem
are as smooth as they can be, and altogether devoid of any
such markings or sculpture as could give rise to the appear-
ance of pores along their line of union*. The syzygial unions
in the rays and arms, however, are sometimes of a slightly diffe-
rent character and present some approach to the condition of
the syzygies in the arms of Comatule. Dr. Carpenter { has
described how each syzygial face in the arm of Antedon rosaceus
is “almost flat, except that it presents a series of slightly ele-
vated ridges with alternating furrows, which radiate from the
opening of the central canal towards the dorsal margin. . . .
The two sets of ridges are applied to each other, leaving
between them flattened passages that are formed by the corre-
spondence of the furrows. ... . An examination of decalci-
fied specimens shows that the canals are occupied by radial
extensions of the ordinary sarcodic basis-substance. The
peculiar arrangement of these suggests that, like the ‘ medul-
lary rays’ of an exogenous stem, they may serve to establish
a communication between the ‘ medullary axis’ of this basis-
substance which occupies the central canal, and the ‘ cortical
envelope’ by which the surface of the segment is invested.”
The coeliac canal rests in a more or less defined furrow upon
the upper or ventral surface of each arm-joint, the so-called
ambulacral groove of the skeleton ; and Prof. Perrier tells us}
that “au niveau des syzygies, la cavité cceliaque communi-
que avec un systéme de cavités rayonnant autour du cordon
nerveux, entourées de muscles et qui jouent évidemment un
role important dans la nutrition de la partie solide des bras.”
This statement contains much debatable matter. In the
first place, one would certainly expect that the contents of
these syzygial cavities would be in communication with the
axial canal from which they radiate, rather than with the
coeliac canal on the ventral surface of the joint ; but in a very
large number of Comatule belonging to the genera Antedon,
Actinometra, and Promachocrinus the axial canal or radial
* Zool. Chall. Exp. part xxxii. pp. 4, 5, 13, pls. xxxi., XXXil., XXxVil.,
xlvii., &c.
_ + Researches on the Structure, Physiology, and Development ot
Antedon(Comatula, Lamk.) rosaceus.— Part I.,” Phil. Trans. 1866, pp.720,
721.
¢ “Résumé de Recherches sur l’organogenie des Comatules,” Zool.
Anzeiger, vill. Jahry. 1885, no. 194, p. 265,
the Morphology of the Echinoderms. 113
centre of the syzygial cavities is separated from the cceliac
eanal, which Prof. Perrier regards as their functional centre
of supply, by more than half the height of the arm-joint.
This is not the case in Antedon rosaceus, the type chiefly
studied by Prof. Perrier; for it has relatively low arm-joints
with a deep ambulacral groove on their ventral surface, so
that there is but a thin layer of limestone between the bottom
of the cceliac canal and the axial canal from which the syzy-
gial cavities radiate. But if Prof. Perrier had had a more
extensive acquaintance with the different types of arm-joint
which occur in the Comatule and with the variations in the
sculpture on their syzygial faces, I cannot but think that he
would have hesitated before making the statement which has
been quoted above.
It will be seen that he agrees with Dr. Carpenter in re-
garding these radiating syzygial furrows as nutritive in func-
tion, though he believes them to be filled with water from
the ceeliac canal, rather than with the sarcodic basis-sub-
stance of the skeleton, which would maintain communication
between the internal and external tissues of the arm-joint, the
latter often reaching a considerable thickness. ‘The origin
of these radiating canals in the central canal of the arm-joints
which lodges the neuro-vascular axial cord certainly agrees
better with the latter theory than with that of Prof. Perrier.
It may be noted, too, that in his first account* of these cavities
in the Comatule, he said not a word about their communi-
cating with the exterior, as they sometimes seem to do in a
dried arm of Comatula, or in a fragment which has been
boiled in potash. He now tells us, however, that in the
Stalked Crinoids (Encrines) these radiating cavities are not
only present at the syzygies, but that they communicate with
the exterior by pores placed at equal distances round the out-
line of the syzygy. Can he name a single Stalked Crinoid
in which the syzygial faces are separated by radiating pas-
sages as in the Comatule and there are pores round the out-
line of the syzygies? Bathycrinus has no syzygies at all;
and there are uo pores or anything resembling them in
Rhizocrinus, Hyocrinus, or Holopus. Prof. Perrier has never
seen a Metacrinus, or he would scarcely have doubted its di-
stinctness from Pentacrinus; and,unless I am greatly mistaken,
he has never had an arm-fragment of the former genus from
which to cut a section through a syzygial union. The only
possible type, therefore, which could have furnished him with
the evidence on which he bases his statements respecting the
* Zool, Anzeiger, 1885, p. 265.
114 Dr. P. H. Carpenter on some Points in
Stalked Crinoids is Pentacrinus itself. Can he name a single
recent species of this genus in which the syzygial faces are
marked by elevated ridges and furrows radiating from the
central canal as in the Comatule? In by far the greater
number of cases the joints are perfectly plain, without any
indications of sculpture at all*; but there is sometimes a
slight trace of striation round the margins of apposed syzy-
gial surfaces. Exactly the same thing often occurs on the
apposed surtaces of the basals and radials respectively, and
on the lateral surfaces of the radials where they are closely
united by suture. Sometimes, indeed, there is a faint indi-
cation, over part of the syzygial face, ef a radial striation
which extends inwards towards the central canal but dies
away before reaching it, and is not due to the presence of
elevated ridges, as in the Comatule. ‘The best instance of this
which I know is on the apposed syzygial faces of the radials
of a Pentacrinus asterius which were figured by Sir Wyville
Thomson in the ‘Challenger’ Report tT; but his figure of the
“yourtour de la syzygie’’ on the dorsal aspect of the ray
shows it to be absolutely devoid of all trace of pores, as is
really the case. I have seen many other indications of radial
striation, both in this and in other species of Pentacrinide ;
but they are merely superficial markings on the joint-faces,
and are altogether different from the well-defined radiating
ridges on the syzygial faces of a Comatula arm-joint, which
can be stripped off entire when the syzygy is split open after
decalcification. It is, of course, possible that Prof. Perrier may
have obtained a section through a syzygy in a Pentacrinus-arm
with better-defined radiating ridges and intervening furrows
than any which I have seen in this genus; but I doubt it.
The dredgings of the ‘ Talisman’ yielded several specimens
of Pentacrinus Wyville-Thomsoni; and if Prof. Perrier has
not cut sections through a syzygy of this species, it would
have been better for him to have done so before making a
general statement respecting the syzygies of Stalked Crinoids
which harmonizes so admirably with his previously expressed
views. I have several sections through the largest syzygy
in this species, viz. that between the second and third radials ;
and there is absolutely no trace either of the radiating cavities
or of the powerful muscles which Prof. Perrier describes in
the “ Enerines.” I can say the same of the arm-syzygies in
Pentacrinus decorus; and if the smooth appearance of the
syzygial faces is any guide, there is not a single recent mem-
* Zool, Chall. Exp. part xxxii. pp. 4, 254, pls. xxvi. & xxxyil.
ap Jel, saat tags, U5 ksh 2a,
—- -¢
the Morphology of the Echinoderms. 115
ber of the Pentacrinide, any more than there is of any otner
family of Stalked Crinoids, with radiating cavities at its
syzygies as described by Prof. Perrier. ven as regards the
Comatule, which do have more or less appearance of external
pores at their syzygies, I cannot accept Prof. Perrier’s asser-
tion as at all consistent with the facts of the case. I do not
deny that pores appear at the syzygies on arms which
have been boiled in potash, as was figured by Dr. Carpenter
in Antedon rosaceus *; but there is a layer of perisome + out-
side the skeleton which is removed by this treatment, so that
the pores appear far more distinctly than they do in a dry
arm, and still more so than in a fresh or spirit-specimen.
This layer of perisome is very well shown in the terminal
parts ot arms which have been stained with picrocarmine
and mounted in dammar; and the syzygial pores are then
seen to be covered by it. ‘The sections which I have made
in three planes through the arms of many species of Comatula
have given me every reason to believe that the pores of the
skeleton do not open to the exterior through this layer of
perisome (which is often much thicker than in Antedon rosaceus)
as Prof. Perrier’s theory requires; while I much doubt
whether the so-called powerful muscles are anything more
than the closely set fibres which form the organic basis of the
elevated radiating ridges on the syzygial faces. It is certainly
very remarkable that the positions assigned to these muscles
by Prof. Perrier are exactly those where the calcareous tissue
is densest, on the syzygial faces of fossil arm-joints. I
have explained elsewhere {| how the organic basis of the
pieces of the skeleton becomes much more close and compact
near those surfaces which are in contact with other joints ;
and I believe this to be preeminently the case at the syzygies,
though the apposed faces are not so perfectly united as in the
case of the basals and radials, for the syzygial unions are
severed with great ease. If Prof. Perrier really does believe
that water is driven out from pores at the arm-syzygies of
Antedon rosaceus, he can prove it in a very simple way. If
he will “ pith” the creature by removing its chambered organ
it will lie still in the water; and the action of the powerful
muscles expelling water from the syzygial pores would surely
cause such a disturbance in the surrounding medium as would
* Phil. Trans. 1866, pl. xxxvi.
+ The “ cortical envelope” of Dr. Carpenter.
t “On the Genus Actinometra, Mull., with a Morphological Account
of a new Species from the Philippine Islands,” Trans. Linn. Soc. 1879,
2nd ser., Zool. vol. i. pp. 55-87,
116 Dr. P. H. Carpenter on some Points in
prove his theory incontestably. Has he performed this expe-
riment or any one which would give the same results?
Even then, however, his theory does not hold good for the
Stalked Crinoids, none of which have any radiating cavities
or pores at their syzygies, while these unions are altogether
absent in Bathycrinus. His assertion that water is expelled
from the coeliac canals of the arms through pores on the.
“ nourtour ” of the syzygies would thus appear to be a some-
what hasty generalization from the supposed condition of the
OComatule. It is essential, however, to his conception of a
Crinoid as a kind of sponge with incurrent and excurrent
openings for the circulation of water. The former are pro-
vided for by the ciliated water-pores on the disc; but where
are the latter in Holopus, Hyocrinus, Bathycrinus, Rhizo-
crinus, and, I will also add, in the Pentacrinide ?
Professor Perrier’s brief notice of the ‘ Challenger’ Report
contains the following passage *:—“ Poussé par on ne sait
quelle prévention assez mal dissimulée contre ce qu'il appelle
un peu dédaigneusement ‘1’école frangaise,” M. Herbert
Carpenter, dont les études ont été terminées 4 |’Université de
Wiirtzbourg (sic), s’est,en bon camarade, jeté téte baissée a la
suite du zoologiste allemand qui a le plus habilement étudié
les Crinoides. II affirme en avoir confirmé presque tous les
résultats dont beaucoup sont cependant erronés, et il ne se
sépare guere de son guide que pour défendre les opinions,
dailleurs exactes, de son pére relativement au systéme ner-
veux.”
The last sentence contains a statement which falls very
considerably short of the truth. Not only do I disagree with
the published views of my old friend Prof. Ludwig respecting
the nervous system of Crinoids, but I have given a different
account of the basals of RAczocrinus from that which he put
forward; and, in common with Mr. Sladen {, I dissent alto-
gether from the theory which he has published concerning
the relations of the Crinoid calyx in the Urchins and Star-
fishes t. I differ from him and from other German writers,
Studer and Hérnes §, upon this purely theoretical point as
* ¢Revue Scientifique,’ May 30, 1885, p. 693.
+ “On the Homologies of the primary Larval Plates in the Test of
eee Echinoderms,” Quart. Journ. Micr. Sci. n. s. vol. xxiv. 1884,
. 00-37.
ee oT bed. vol. xx. 1880, pp. 822-329; and “Notes on Echinoderm Mor-
phology.—No. V. On the Homologies of the Apical System, with
some Remarks upon the Blood-vessels,” Jbzd. vol. xxii. 1882, pp. 376-
on “On the Apical System of Ophiurids,” Zéd. vol. xxiv. 1884, pp. 16-
18; and Zool. Chall. Exp. part xxxii. pp. 392-400.
the Morphology of the Echinoderms. 117
strongly as I do from the French authors, Messrs. Perrier,
Koehler, and Apostolidés, respecting the supposed communi-
cation with the exterior of the so-called blood-vascular sys-
tem in Urchins and Ophiurids, through the pore-canals of the
madreporite. It is on this last pomt, which deals with fact
and not with theory, that, like Ludwig, I am at variance with
-what | ventured three years ago to call ‘the French school.”
My reasons for the “ prévention ”’ referred to by Prof. Perrier
are twofold.
In the first place, I do not believe many of their statements
of fact to be correct, as I distrust the nature of the evidence upon
which these are based; and, secondly, there is far too strong a
tendency, especially in the case of Professor Perrier, to make a
sweeping generalization upon data which are either altogether
inadequate or even absolutely incorrect. An excellent in-
stance of the latter kind is afforded by Prof. Perrier’s state-
ment respecting the presence of radiating cavities at the
syzygies of the Stalked Crinoids, which I have discussed
above.
The greater part of his publications upon the morphology
of the Crinoids have been limited to what he himself de-
scribes* as “quelques fragments isolés” of his results.
Some of his earlier statements have been profoundly modified
in later communications, while others have been tacitly with-
drawn. Among the latter, for example, is the expression of
his conviction that no one will ever find the coeliac canal of a
Crinoid J, although he now tells us that 1t communicates with
the exterior through pores at the syzygies of the arms. After
having once asserted that the cirrus-stumps of a Pentacrinoid
larva alternate with those of the arms tf, in spite of the evi-
dence to the contrary in the descriptions and figures of
Dr. Carpenter § and M. Sars||, Prof. Perrier now tells us ¥
that the cirri and the arms are “superposed,” a fact that
has been known for the last twenty years. Then, again,
Prof. Perrier ** claims to have “‘ démontré”’ that the inter-
* Zool. Anzeiger, 1885, p. 267.
+ “Recherches sur Anatomie et la Régénération des Bras de la
Comatula rosacea,” Arch. de Zool. Expér, et Génér. t. ii. 1873, pp. 48, 49,
73.
{ “Sur la développement des Comatules,” Comptes Rendus, tom. xcviii.
1884, p. 446.
§ Phil. Trans. 1866, pls. xl., xli.
| ‘Crinoides vivants,’ tab. v. p. 53.
q Zool. Anzeiger, 1885, p. 264.
__** “Sur une Astérie des grandes profondeurs de l’Atlantique, pourvue
dun pédoncule dorsal,” Comptes Rendus, t. xcv. 1882, p. 1381.
118 Dr. P. H. Carpenter on some Points in
radial abactinal plates of the young Brisinga eventually
become the odontophores; and upon this supposition he
based a generalization concerning the whole of the Asterids.
As a matter of fact, however, he was merely repeating a
statement made some time previously, but never satisfactorily
proved; while its accuracy has since been questioned by
Sladen *, who has also proved beyond all doubt that, what-
ever be the case in Bristnga, Prof. Perrier is utterly at fault
with regard to the fate of the interradial abactinal plates in
other Starfishes.
According to Prof. Perrier, it has been demonstrated by
himself, together with Koehler and Apostolides, that the
blood-vascular system of Urchins and Ophiurids communi-
cates directly with the exterior through the madreporite.
But I have pointed out elsewhere T that no valid proof of this
statement has ever been furnished to morphologists, except an
account of the results of injections. J may be peculiar, but I
do not believe in the injection method as a means of settling
intricate anatomical questions. Sometimes, as Ludwig has
shown in the case of Greeff and Hoffmann, it proves, or rather
appears to prove, far too much ; while in other cases it gives
altogether insufficient results. Some years ago, in conse-
quence of unsuccessful injections, Prof. Perrier was led to
deny the existence of what is generally known as the blood-
vascular ring of Hehinus, and of a vessel which had been sup-
posed to connect it with the so-called heart or ovoid gland tf.
His friend Mons. Koehler, however, was able to demonstrate
the presence of these organs without difficulty; and he con-
firmed the results of his injections by the section-method §.
But neither Koehler, Perrier, nor Apostolidés has figured a
single section which shows how the ovoid gland of any Urchin
or Ophiurid communicates with the exterior; though their
injections have caused them to speak of it as a demonstrated
truth about which there can be no doubt whatever ||. Lud-
wig’s careful sections and dissections of the madreporite of a
Starfish, however, have led him to the conclusion, which his
* Quart. Journ. Micr. Sci. n. s. vol. xxiv. pp. 39-41.
t+ “Notes on Kchinoderm Morphology.—No. VI.,” Jbzd. vol. xxiii.
pp- 597-609 ; No. IX. Zéed. Supplement, 1885, pp. 15-18 (of separate
copy):
iL ! Sur l Appareil circulatoire des Oursins,” Comptes Rendus, Noy. 16,
1874; and “ Recherches sur l’ Appareil circulatoire des Oursins,” Arch.
de Zool. Exp. et Gén. t. iv. 1875, p. 615.
§ “Recherches sur les Echinides des Cotes de Provence,” Ann. du
Mus. d’Hist. Nat. de Marseille, Zoologie, Mém. no. 3. pp. 65-70,
|| R. Koehler, “ Quelques mots sur les relations du systéme circulatoire
chez les Echinides,” Zool. Anzeiger, Jahrg. viii. 1885, p. 81.
the Morphology of the Echinoderms. 119
figures fully bear out, that the pore-canals of the madreporite
lead into the water-vascular apparatus only, and have abso-
lutely no connexion with the blood-vascular system *.
These statements have never been contradicted by Professor
Perrier, who has nowhere described any such communication
between the water-vascular and blood-vascular systems of a
Starfish as he believes to exist in Urchins and Crinoids.
But all the same, he places the Starfishes, together with the
other Echinoderms, in the same division of the Metazoa as
the Polypes and Sponges. The bodies of the animals com-
posing this group, which he calls “‘ Zoophytes,” are traversed
by a set of irrigating canals T—“ II contient de méme, non
pas de sang, mais de l’eau qu’il puise incessamment au dehors
et se substitue tout 4 la fois a l’appareil circulatoire et a
Vappareil respiratoire des animaux mobiles, 4 la symétrie
bilaterale, avec lesquels il n’a aucun rapport morphologique.
On doit remarquer que, chez les échinodermes, il dérive au
moins indirectement de la cavité digestive primitive.”’
This conception of the mode of nutrition of Echinoderms
is well described by Prof. Perrier as both ‘ simple and new ;”
but he can scarcely expect it to be adopted by other naturalists
until he can demonstrate to their satisfaction the fundamental
unity of the double vascular system and its communication
with the exterior not only in Kchini, Ophiurids, and Crinoids,
but also in Starfishes and Holothurians, about which groups -
he has given us no positive information at all.
My own observations have led me to believe that the state-
ments which he has permitted himself to make concerning
the presence of excurrent openings in the arms of Stalked
Crinoids are absolutely without any foundation of anatomical
fact. But they harmonize with his theories of Crinoid mor-
phology in a way which leaves nothing to be desired for
completeness; and I have a strong suspicion that some of his
other assertions respecting the vascular system of the Kchi-
noderms are equally untrustworthy, as, indeed, has been
already proved by Koehler. Other investigators are at work
upon the subject, and we may hope to hear a good deal about
it before many months are past.
* “ Beitrige zur Anatomie der Asteriden,’ Zeitschr. f. wiss. Zool.
Bd. xxx. 1878, p. 104.
+ ‘Revue Scientifique, May 30, 1885, p. 692.
120 Mr. J. A. Murray on a
XIII.—Description of a new Species of the Zetides Section of
: Papilio. By F. Moors, F.Z.8., A.L.S.
Zetides Acheron, n. sp.
Nearest to Z. Avion. Upper side differs in the medial trans-
verse band being broader, the discoidal spots longer, and the
marginal spots larger. Underside: markings more nacreous
than in Z. Axion or Z. Telephus : fore wing with the medial
transverse band much broader throughout and very slenderly
divided by the veins ; discoidal spots all larger, the two termi-
nals well separated, the penultimate upper spot entire: hind
wing with a very broad medial band of wider extent than in
Z. Evemon; the subbasal costal red-banded streak also broad ;
the black spot at end of the cell linear and narrow, with the
red lunule situated outside the cell between the lower sub-
costal and radial vein ; a red lunule (but no preceding black
spot) between the radial and upper median; the other two
succeeding black spots being quadrate, and their red lunule
recurved ; the marginal row of spots of a conical shape, their
upper end almost touching the red lunules.
Expanse 3} inches.
Hab. N.E. Bengal. In coll. F. Moore.
XIV.—A new Frog (Rana sternosignata) from Sind. By
James A. Murray, Curator of the Kurrachee Municipal
Museum.
In this paper I have to add a Batrachian to the already known
forms in Sind.
I am indebted for the specimens to Captain J. Babington
Peile of the P. W. own Grenadiers, who very kindly under-
took to make a collection of specimens for the Kurrachee
Museum, when on the Zhob Valley expedition, and to Mr. J.
Strachan, M.I.C.E., of the Kurrachee Municipality. Capt.
Peile’s specimens are from Zandra in Afghanistan and Quetta,
and Mr. Strachan’s from Mulleer near Kurrachee.
Rana sternosignata, sp. nov.
Head broad, without an occipital fold. Gape 1-5 inch across.
Snout rounded, without canthus rostralis, nostrils nearer the
eye than the end of the snout. ‘Tympanum rather indistinct,
about one third the size of the eye. Jnterorbital space slightly
concave and as wide as the upper eyelid. A plait behind the
eye above the tympanum not very distinct in some speci-
new Frog from Sind. - 121
mens. Vomerine teeth in two small groups between the inner
nostrils. Lower jaw with two not very prominent apophyses.
Back and upper surface of hind limbs finely tubercular. Sides
rugose, with spiniferous warts. On the under surface there
are two nearly circular patches of minute dark spinescent tuber-
cles on the sternum, and the abdomen 1s covered with large
horny-tipped tubercles, while under the throat and, in some
specimens, on the chin also there are patches of minute spinous
granulations. Fore limb short and stout; fingers of mode-
rate length, the tips dilated into small disks ; subarticular
tubercles well developed. Palmar surface of both fore and
hind feet with minute, scattered, conical, dark spinous tuber-
cles. Laid side by side the second and fourth fingers are equal,
the first smallest and the third longest. irst finger with a
nodose prominence covered with minute tubercles on the dorsal
surface ; second finger the same, with the nodose prominence less
developed, while below, on the side of the first finger, is also a
thumb-like prominence covered with tubercles. Hind limbs
moderate. ‘The distance between vent and knee equals half
the length of the head and body. Laid forward, the knee
reaches the axil of the fore limb and the metatarsal tubercles
the tip of the snout. ‘The toes are webbed to the base of the
disks or swollen tips, and bear subarticular tubercles; meta-
tarsus with a single elongate spur-like tubercle. A cutaneous
fringe along the margin of the first and fifth toes.
Colours. Krom olive-brown to dark brown on the dorsal
surface; yellowish brown on the ventral surface, with or
without, or with a very few dark brown specklings. Chin and
throat yellowish white, more or less marbled with brown.
Inner side of thighs brownish, with flocculent yellowish
marbling.
_ Locality. Mulleer near Kurrachee ; Zandra and Quetta, in
South Afghanistan.
In general characters this species is not unlike R. cyano-
phlyctis, but is readily recognized by its broad head, sternal
tubercular patches, and tubercular thumb-like nodosity below
the first finger, as also by the tubercular dorsal surface of the
first and second fingers.
XV.—Description of two new Curculionide (Ectemnorhinus)
from Marion Islands. By CHARLES O. WATERHOUSE.
THE specimens which are the subject of this note were col-
lected during the ‘ Challenger’ expedition (on Dec. 26, 1873),
122 Mr. C. O. Waterhouse on new Curculionide.
but were accidentally omitted in my account given in a former
number of this journal (Ann. & Mag. Nat. Hist. xii. 1884,
p- 276). The discovery of two new species of the genus
Ectemnorhinus, the species of which have hitherto only been
found in Kerguelen, is interesting, especially as they are
somewhat intermediate in their characters between H. viridis
and H. angusticollis in the case of the larger species, and
between ZL. gracilipes and E. brevis in that of the smaller.
Lctemnorhinus similis, n. sp.
Brunneus, sparsim viridi-flavo-squamulosus ; elytris fortiter striatis,
striis punctatis.
Long. 3} lin. (7 millim.).
This species is somewhat intermediate between LE. viridis
and H. angusticollis*, but differs from both in being sparingly
covered with minute elongate scales. The antenne are very
similar to those of H. viredis, but a trifle longer. The first
and second joints of the funiculus are long, the first being a
little longer than the second, whereas in /. viridis the first is
a little shorter than the second; the third and fourth joints
are at least as long as broad; the fifth, sixth, and seventh joints
are a little shorter. The thorax is considerably narrowed in
front and behind, convex, with a very slight indication of a
median carina. LElytra at the base a little broader than the
thorax (with distinct but very obtuse shoulders), considerably
broader posteriorly ; strongly striated, the strie rather strongly
punctured ; the apex of each elytron broadly rounded. The
claw-joints are rather larger than in #. viridis, but not nearly
so large as in H, Hatoni (Ent. Mo. Mag. xiii. 1876, p. 51).
Slightly immature specimens have the legs yellow, and
sometimes the elytra are yellowish.
Ectemnorhinus parvulus, n. sp.
Niger, parce viridi-squamulosus; antennis gracilibus; thorace
angusto, medio carinato ; elytris obovatis, fortiter striatis, striis
fortiter punctatis.
Long. 4 millim.
This could only be confounded with Z. gracdlipes, which it
closely resembles in general form and colour. It is, however,
a little shorter, and more ample posteriorly. The funiculus
of the antenne is much more slender; the first and second
joints long and slender, the third and fourth shorter, the fifth
and sixth a trifle longer than broad, the seventh nearly globular.
* Fide Ent. Mo. Mag, xii. (1875) p. 55.
Mr. R. Kidston on Ulodendron. 123
The rostrum is distinctly longitudinally impressed, the im-
pression bordered on each side by an obtuse ridge. ‘The disc
of the thorax has a short but distinct ridge. The elytra are
obovate, more strongly striated than in LE. gracilipes, the striz
strongly punctured ; the scales on the interstices long and
narrow, but not hair-like as in H. gracilipes.
This species has the shoulders of the elytra bounded by a
distinct ridge as in H. brevis, but that is a short and broad
insect.
These specimens having been in alcohol it is probable that
the paucity of scales may be due to abrasion.
XVI.—On the Relationship of Ulodendron, Lindley and
Hutton, to Lepidodendron, Sternberg; Bothrodendron, Lind-
ley and Hutton; Sigillaria, Brongniart ; and Rhytidoden-
dron, Boulay. By Ropert Kipsron, F.G.S.
[Plates III.-VII.]
AT the meeting of the Royal Physical Society of Edinburgh,
held on 21st March, 1883 *, I exhibited several specimens of
the so-called genus Ulodendron, Lindley and Hutton. I then
stated that I did not regard Ulodendron as forming a true
genus, nor as entirely belonging to Lepddodendron, as some
authors seemed to suppose; but that the genus, as usually
employed by those who believe in its individuality, includes
plants belonging to the genera Lepidodendron, Sigillaria, and
Rhytidodendronyt.
Almost all the misconceptions on the true affinities of UJo-
dendron have arisen through the neglect of a very essential
element for the right understanding of these fossils, and one
which only requires to be mentioned to be fully agreed in
by all botanists, viz. that only well-preserved examples should
be taken into consideration when critically considering the
affinities of this genus; unfortunately this has not always
been observed.
When determining the various species of the genera Lepi-
dodendron and Sigillaria, unless the outer surface of the bark
is well preserved and exhibits the form and arrangement of
the leaf-scars, it is admitted that the plants do not show the
* Proc. Royal Phys. Soc. Edin. vol. vii. p. 356 (1483).
+ Boulay, ‘ Le terr. houil. du nord de la France et ses végét. fossiles,’
p. 89 (Thése de Géologie), Lille, 1876.
124 Mr. R. Kidston on the Relationship
characters by which a specific, or even in some cases a generic,
determination can be made.
In Ulodendron, on the other hand, though it is difficult to
account for it, decorticated and badly-preserved specimens, if
only they show the characteristic Ulodendroid scar of the
genus, have often been regarded as in a sufficiently good state
of preservation, not only for generic identification, but even
for the creation of new species, notwithstanding that the close
affinity of Ulodendron and Lepidodendron, both in regard to
their internal structure and general characters, is fully recog-
nized. The form and size of the Ulodendroid scar have com-
monly been made the characters on which the various species
of Ulodendron have been founded, the descriptions generally
mentioning as the chief distinguishing point “ scar so long by
so broad.”” Such arbitrary specific distinctions to be of any
value must infer that the plant sprang into existence with the
Ulodendroid scars fully developed. This view of course was
never intended by the authors who described the various
species characterized as indicated above; but to make the
species of true value an inference of this nature is quite
legitimate.
Before entering further on the discussion of this subject it
is desirable to give an epitome of the views which have
been held by the many botanists who have written on it.
As it is now universally admitted that Ulodendron is
Lycopodiaceous, no note is taken of the different opinions on
this point which some of the older writers have advocated,
who in turn allied it to the Conifer, Cactaceee, &c.
In support-of the views I have stated in regard to the genus
Ulodendron, 1 shall describe specimens of three species of
plants which bear Ulodendroid scars ; and as these are plenti-
ful at certain localities in Great Britain I have been enabled
to study many beautifully preserved examples. ‘The results
of these investigations I now beg to lay before the readers
of the ‘ Annals.’ This I especially desire to do, as it explains
more fully than could be done, without the aid of figures, the
views adopted in the classification of these plants in the
‘Catalogue of the Paleozoic Plants in the British Museum.’
The three species specially to be examined are :—
1. Lepidodendron Veltheimianum, Sternberg.
2. Sigillaria discophora, Konig, sp.
3. Sigillaria Taylort, Carruthers, sp.
I am sorry that it will be necessary to criticize the writings
of several friends with whose views on Ulodendron 1 cannot
of Ulodendron to Lepidodendron, cc. 125
entirely agree. I hope, however, that the evidence here brought
forward may be considered a sufficient foundation for the
opinions I have adopted.
The subject is treated under four divisions :—
I. Epitome of the views of previous writers on Uloden-
dron.
II. Descriptions of specimens.
III. General conclusions.
IV. Synonymy and Notes on the three species specially
considered in this communication.
I. EPITOME OF THE VIEWS OF PREVIOUS WRITERS ON
ULODENDRON.
1817. Steinhauer. American Philosophical Society, vol. i.
new series. (Communicated May 2, 1817.)—The earliest
figured fossil plant which can be referred to Ulodendron,
Lindley and Hutton, appears to be that described by Stein-
hauer in 1817 as Phytolithus parmatus.. Under this name,
however, he included two plants which belonged to distinct
genera. His fig. 1, pl. vi., is referable to Calamitina, Weiss,
and is probably Calamitina Germariana, Géppert, sp. *; that
on pl. vil. fig. 1 is referable to Leptdodendron, and though
the specimen does not show the form of the leaf-scars di-
stinctly, the general character of the fossil points to the pro-
bability of its belonging to Lepidodendon Velthetmianum,
Sternberg.
1820. Rhode. Beitriige zur Pflanzenkunde der Vorwelt.
—Under the somewhat comprehensive title of “ Schuppen-
pflanzen,” this author gives, on pl. iu. fig. 1, a very fair
figure of Lepidodendron Veltheimianum, showing the Uloden-
droid scars. On the lower part of these sears (on the upper
part, as represented by Rhode, whose figure is inverted) are
seen the remains of the leaf-scars, and on the isolated Ulo-
dendroid scar, figure 4B of the same plate, the medial line of
the leaf-scar is clearly indicated. Rhode believed that the
Ulodendroid scars on this specimen were flowers, the leaf-
scars on its surface the petals. Although this view is crude,
his drawings of Ulodendron are not so inaccurate as is
sometimes supposed. The other figures which he gives of
these Ulodendroid Lycopods have not been taken from well-
preserved specimens.
* Weiss, “Steinkohlen-Calamarien” (Abhandl, zur geologischen Special-
karte von Preussen und den Thiiringischen Staaten, Band ii. Hett 1),
p. 126 (1876). Cyeclocladia major, Lindley and Hutton, ‘ Fossil Flora,’
vol. ii. pl. cxxx., also appears to be referable to Calamitina, Weiss.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 10
126 Mr. R. Kidston on the [Ielationship
1823. Allan. ‘“ Description of a Vegetable Impression
found in the Quarry of Craigleith,” Trans. Roy. Soc. of Edin-
burgh, vol. ix. p. 235, pl. xiv. (Read Jan. 22, 1821.)—
The figure given by Allan is a beautiful example of Lepido-
dendron Veltheimianum, showing the large Ulodendroid scars.
This fossil is now in the Museum of Science and Art, Edin-
burgh, and is also the subject of pl. xvin. vol. ir. of Brongniart’s
Hist. d. végét. foss. A reduced figure of the same specimen
is likewise given by Buckland in his ‘Geology and Mine-
ralogy,’ vol. 1i. pl. Ixxvi. fig. 3; and, finally, Mr. Carruthers has
figured a single Ulodendroid scar from the same example in
the ‘ Monthly Microscopical Journal,’ vol. ii. pl. xliv. fig. 4.
Allan regarded the large scars as the impressions of flowers
or fruit.
1825. Konig. Icones fossilium sectiles. (London.)—There
is here figured on pl. xvi. fig. 194, without any description, a
specimen of Ulodendron which Konig names Lepidodendron
discophorum. 'This seems similar to the plant subsequently
described as Ulodendron majus by Lindley and Hutton.
1826. Sternberg. Essai d'un exposé géognostico-bota-
nique de la flore du monde primitif, fase. iv. p. xi Ulo-
dendron is here placed in the group “ Hilices vere,” under the
name of Lepidodendron ornatissimum. Sternberg believed that
the large scars marked the attachment of fronds to the stem.
1828. Brongniart. Prodrome d’une histoire des végétaux
fossiles, p. 85.— Ulodendron is also included among the Lepi-
dodendra by Brongniart, by whom it is called Lepidodendron
ornatissimum, Sternberg.
1831. Lindley and Hutton. Fossil Flora of Great Britain,
vol. i. pls. v., vi.—The name of Ulodendron was first applied
to these fossils by Lindley and Hutton, whose genus may be
defined as follows:—Stem covered with rhomboidal leaf-
scars, and bearing two opposite rows of large circular or oval
scars, indicating points from which “ branches, or, more pro-
bably, masses of inflorescence,” have fallen.
Their genus Bothrodendron (Fossil Flora, vol. ii. pls. xxx.,
lxxxi.) is merely a decorticated condition of Ulodendron,
notwithstanding that one of their descriptions is headed ‘‘Cor-
ticated”” (to pl. Ixxx.) and the other “ Decorticated”’ (to
1. Ixxxi.). This point will be further remarked on.
1837. Buckland. Geology and Mineralogy, vol. i. p. 475,
and vol. ii. pp. 92-95.—Buckland adopts the views expressed
by Lindley and Hutton, that the large circular or oval pits
were caused by. the pressure of cones on the bark, which sub-
sequently grew up round their base. He also regarded the
genus Bothrodendron, L. & H., as distinct from Ulodendron.
of Ulodendron to Lepidodendron, &c. 127
He defined Ulodendron as follows :—‘ Stem not furrowed,
covered with rhomboidal marks. Scars of cones circular ;”
and Bothrodendron— Stem not furrowed, covered with dots.
Scars of cones obliquely oval.” Buckland believed that the
cones were only attached to the centre of the large scars, and
that the furrows on the upper parts of the scars, which radiate
from the umbilicus, were formed by the scales at the base of
the cone pressing against the bark.
1837. Brongniart. Histoire des végétaux fossiles, vol. ii.
p- 69.—Brongniart, as in his ‘ Prodrome,’ here places
Ulodendron among the Lepidodendra. On pl. xviii. he gives
a figure of Lepidodendron Velthetmianum under the name of
Lepidodendron ornatissimum ; on pl. xix. four other figures
of Ulodendra are given under the name of Lepidodendron ;
one of these (fig. 1), at least, if not all, belongs to Stgillaria
discophora, Konig, sp.=(U. majus, L. & H.). Brongniart
points out the peculiar character of the bark becoming fissured
in those examples which bore the Ulodendroid scars, which is
a character not common to most Lepidodendra. 'The presence
of these furrows he thought indicated that the specimen pos-
sessing them belonged to the lower part of the stem, and that
they were caused by adventitious roots bursting through the
bark.
He argues that had the large scars been originally
covered with the ordinary cauline leaves, they should follow
the ordinary spiral series of the stem, which he says they do
not, each disk showing in the cicatrices which cover it a series
of spirals peculiar to itself*. Or if they were the impressions
of the scales of the cone, which had completely effaced
from the surface of the stem all traces of the organs that it
bore, then the impressions of the appendicular organ on the
stem should have been in an inverse order from the leaf-
scales of the stem, because the extremities of the scales of the
cone are convex and should have made depressions on the
stem. On the contrary, the marks presented on the Uloden-
droid scars are similar to those of the leaves on the stem.
1848. Hooker. “On the Vegetation of the Carboniferous
Period as compared with that of the present Day,” Memoirs
of the Geological Survey of Great Britain, vol. u. part i.
p: 427.—Of Ulodendron, Sir Joseph Hooker says :—“ This
very remarkable genus scarcely differs from Lepidodendron
in internal structure: its external aspect widely differs from
that of any plant, recent or fossil, with which I am ac-
quainted. I have seen in collections specimens which have
been fossilized, apparently erect, or, at any rate, under very
* See description of specimens Nos. 3 and 7.
Os
128 Mr. R. Kidston on the Relationship
different circumstances from those preserved in the shales over
the coal. They present the appearance of a large unbranched
zigzag trunk, with two rows (opposite one another) of alter-
nating cup-shaped deep depressions, one at every projecting
angle of the trunk. Mr. Dawes showed me a specimen pre-
served in sandstone, with a large organ, which he considers a
cone, inserted into one of the cup-shaped depressions. I
could not, however, form any conclusion concerning the real
nature of this highly interesting example.”
1848. Sauveur. ‘ Véeétaux fossiles des terrains houillers de
la Belgique,’ Académie royale d. sciences, d. lettres et d.
beaux-arts de Belgique.—On pl. Ixvi., under the name of
Arthrocladion Rhodii,is figured a large decorticated specimen of
Ulodendron, representing that condition of the plant for which
Lindley and Hutton proposed their genus Bothrodendron.
1849. Brongniart. Tableau des genres de végétaux fossiles,
p. 42.—Brongniart here states his belief that Ulodendron
may be only founded ona peculiar condition of Lepidodendron,
but which, from the occurrence of the large circular scars,
may perhaps deserve to be generically distinguished.
1850. Unger. Genera et species plantarum fossilium,
p- 262.—Ulodendron is here regarded as forming a true genus,
with which, however, is united Bothrodendron, L. & H.
1852. Goppert. ‘TFossile Flora des Uebergangsgebirges,”
Verhandl. der Kaiserl. Leop. Carol. Akad. d. Natur. vol. xxu.
supp!.—In this work Géppert mentions four species of Mega-
phytum. One of these at least, his Megaphytum dubium,
belongs to the so-called genus Uledendron. Géppert himself
expressed doubt as to the propriety of keeping this separate
from Lepidodendron Veltheimianum; and on p. 191 he says:
“ T confess I am still in doubt concerning the existence of this
species, it many times having appeared to me as belonging to
SagenariaVeltheimiana.” ‘lhe specimen to which his remarks
apply (pl. xxv.) cannot be placed in Megaphytum, and
clearly belongs to Ulodendron, L. & H. ‘The general cha-
racter of Megaphytum dubium shows a great similarity (espe-
cially in regard to the arrangement and form of the large
sears) to Ulodendron Taylori, Carr.; but from the fossil
being decorticated, its specitic identity cannot be satisfactorily
determined.
1853. Tate. In the ‘ Natural History of the Eastern Bor-
ders,’ by G. Johnston. (London.)—This author says on p. 302 :
“The Ulodendron was the most singular plant which flourished
during the Carboniferous era. Specimens obtained from Aln-
wick Moor enable us to add something to the knowledge of
its form. Its internal structure is the same as that of Lepido-
of Ulodendron to Lepidodendron, &c. 129
dendron ; it possessed similar leaves and rhomboidal areole
on the stem and branches. A specimen in Alnwick Castle
shows that its mode of branching is dichotomous, like the
Lepidodendron ; but, in addition, there are rows of round or
oval scars on opposite sides of the stem arranged vertically ;
and these scars continue upward on the same plane along the
branches, while other rows commencing at the point of forking
run up on the opposite side of the branches; the scars and
the branches are all in the same plane. ‘These scars appear
to have been points of attachment of masses of inflorescence,
which had consisted of sessile cones formed of imbricated
scales in a manner similar to a fir-cone. ‘The chief difference
between Lepidodendron and Ulodendron would therefore be
that the cones, bearing sporules or seeds, were placed at the
end of branches on the former, but their position on the
latter was in linear rows on the stem and branches.”
The only species Tate mentions is Ulodendron ornatissi-
mum, Sternberg, sp. Of this he says: “ The fruit-scars of
this species are large and beautifully sculptured; we have
them 11 inches in circumference; the distance from each
other varies—in some specimens they are in contact, in
others 1 inch apart; the areole also vary in form; when
well preserved they are rhomboidal, contiguous, and spirally
arranged. Buckland’s U. Allani, and Brongniart’s ZL. orna-
tissimum are representations of different portions of the same
species.”
1854. Geinitz. Darstellung der Flora des Hainichen-
Ebersdorfer und des Fl6haer Kohlenbassins.— Underthe name
of Sagenaria Veltheimiana, Geinitz figures:some fine exam-
ples of Lepidodendron Veltheimianum, showing the Uloden-
droid condition (pls. iv., v.).
1855. Geinitz. Die Versteinerungen der Steinkohlen-For-
mation in Sachsen, p. 34.— Ulodendron is again placed in Lept-
dodendron by Geinitz. He says: “The branch-scars stand
quincuncially and sometimes in only two rows ;”’ and, again,
“The occurrence of these large branch-scars has given rise to
the formation of the genus Ulodendron.”
1855. Goldenberg. Flora Sarepontana fossilis. Die
Pflanzenversteinerungen des Steinkohlengebirges von Saar~
briicken, p. 18. Genus Ulodendron.— This author regarded
the large Ulodendroid scars as marking the place from which
cone-like branches had fallen, these cone-like branches being
formed through the arrested development of ordinary lateral
branches.
1857. Miller. Testimony of the Rocks, pp. 462 & 464.—
On p. 462 Hugh Miller says: “The only terminal point of
130 Mr. R. Kidston on the Relationship
Ulodendron I ever saw was nearly as obtuse as that of Stzq-
maria.” [Note-——The Stigmaria to which he refers is shown
in a woodcut, p. 462 (fig. 128), of the same work. ‘This
example exhibits a truncated extremity.]
1860. Eichwald. Lethea Rossica, vol. 1. p. 137.—Ulo-
dendron, in which is included Bothrodendron, is treated by
Eichwald as forming a true genus. He believed that cones
were attached to the Ulodendroid scars. Some of his figures
are very instructive, and will be more fully referred to again.
1864. Macalister. Journ. Royal Geol. Soc. of Ireland, vol.i.
—This writer suggests that Ulodendron might perhaps be
Cycadaceous. He also points cut the probable identity of Ulo-
dendron majus and U. minus.
1868. Dawson. Acadian Geol. 2nd ed. p. 454.—Under
the name of Lepidophloios Dawson includes ‘ those Lycopo-
diaceous trees of the Coal-measures which have thick branches,
transversely elongated leaf-scars, each with three vascular
points and placed. on elevated or scale-like protuberances, long
one-nerved leaves, and large lateral strobiles in vertical rows
or spirally disposed ;” and he says :—‘‘ Regarding L. laricinus
of Sternberg as the type of the genus, and taking in connexion
with this the species described by Goldenberg and my own
observations on numerous specimens found in Nova Scotia, I
have no doubt that Lomatophloios crassicaulis of Corda and
other species of that genus described by Goldenberg, Ulodendron
and Bothrodendron of Lindley, Lepidodendron ornatissimum of
Brongniart, and Halonia punctata of Geinitz, all belong to this
genus, and differ from each other only in conditions of growth
and preservation. Several of the species of Lepzdostrobus
and Lepidophyllum also belong to Lepidophloios. ‘The species
of Lepidophloios are readily distinguished from Lepidoden-
dron by the form of the areoles and by the round scars on
the stem, which usually mark the insertion of the strobiles,
though in barren stems they may also have produced
branches ; still, the fact of my finding the strobiles 7 sééw in
one instance, the accurate resemblance which the scars bear
to those left by the cones of the red pine when borne on thick
branches, and the actual impressions of the radiating scales in
some specimens, leave no doubt in my mind that they are
usually the marks of cones; and the great size of the cones
of Lepidophlotos accords with this conclusion.”
1869. Carruthers. ‘On the Structure of the Stems of the
Arborescent Lycopodiacese of the Coal-measures (Ulodendron
_ minus, Lindl. & Hutt.),”’ Monthly Microse. Journ. Nov. 1869,
p- 225.—The internal structure of the plant is described.
Mr. Carruthers says of Megaphyton, which he unites with
of Ulodendron to Lepidodendron, cc. 131
Ulodendron, “ Megaphyton is based upon amorphous casts of
a portion of the interior of the stem of Ulodendron’’*.
1869. Rohl. “ Fossile Flora der Steinkohlen-Formation
Westphalens, einschliesslich Piesberg bei Osnabriick,”’ Paleeon-
tographica, vol. xviii. p. 138.—Ulodendron is regarded
here as a subdivision of Leptdodendron, and only separated
from this latter genus by the presence of the “ large branch-
scars.”
1870. Carruthers. “On the Nature of the Scars in the
Stems of Ulodendron, Bothrodendron, and Megaphytum, with
a Synopsis of the Species found in Britain,’ Monthly Microse.
Journ. vol. i. p. 144.—For specific distinctions in Uloden-
dron, which he believes to form a true genus, Mr. Carruthers
places great value on the form of the umbilicus at the ‘ base
or centre of the pit.” Speaking of the Ulodendroid scars, he
remarks on p. 148: ‘‘ There is not the slightest indication of
scales in any of the large series of specimens I have examined.”
. . . “In attempting to make obvious what authors believed
to be there, the drawings of Ulodendron frequently exhibit
seale-markings.” In proof of this statement he cites Buck-
land’s and Brongniart’s figures of the specimen originally
figured by Allan; and it must be admitted that in these two
eases the leaf-scars are much more prominent on the Uloden-
droid scars than in the original, which is, as already men-
tioned, fortunately preserved in the Museum of Science and
Art, Edinburgh. Mr. Carruthers also believes that the appen-
dicular organ was articulated to the whole surface of the
Ulodendroid scar, and constructs a diagram to explain how
the vascular-bundle-scars on the surface of the large scars
appear as little dots on its lower portion and as elongated
furrows on its upper part. He says, p. 149: “‘ The vascular
bundles, rising upwards and outwards trom the circumference
of the vascular cylinder, would, in passing into the appen-
dicular organ, penetrate the lower half of the articulating
surface at right angles, and would consequently show as
circular pits on the cicatrice ; while the bundles on the upper
half would penetrate the surface at a very oblique angle, and
would consequently show in the cicatrice as more or less
elongated furrows.” ... ‘‘In species like U. transversum,
where the inverted cone of the scar has a descending direc-
tion, the smaller will necessarily have a more or less furrowed
* Norre.—Megaphyton, Artis. I fear Mr. Carruthers cannot have seen
good specimens of Megaphyton, as the scars on the stem of this genus,
when well preserved, ditter much from Ulodendroid scars. There appears
no reason to doubt the correctness of the generally accepted view that
Megaphyton is the stem of an arborescent fern.
132 Mr. R. Kidston on the Relationship
aspect on the lower as well as the upper half of the scar.
That the appendages were articulated to the stem by the
whole surface of the scar cannot be doubted. In the want,
however, of any observed specimen it is not so easy to deter-
mine what these appendages were. The specimen figured on
pl. xliii. fig. 5 appears to me to throw considerable light on
this matter. In this species the opposite ‘series of scars are
borne on swellings on the stem, and the downward aspect of
the scars shows that the organs which sprang from them had
a descending direction. That this is the true position of the
stem is abundantly established by the dark carbonaceous
patches which here and there are attached to it, and which
are the bases of the leaves converted into coal. One of these
patches from the other side of the stem from that shown in
the drawing is represented the size of nature at fig. 6, and
here it is seen that the traces of the leaves still remaining are
imbricated over each other, and that the scars where the leaves
are broken off are on the upper portion of each base. ‘This
clearly shows the natural direction of the specimen figured.
The appendages, then, must have been adventitious roots in
this specimen*. Inthe light of this specimen the form and direc-
tion of the scars, where their original depth is to any extent
preserved, appear to corroborate this view. ‘The appendage
could not in any of them have been patent; indeed they seem
to show that it must have passed out outwards and down-
wards.”
Bothrodendron and Megaphytum are united by Mr. Car-
ruthers with Ulodendron, which genus he describes as
follows :—‘‘ Stem covered with rhomboidal scars of leaves,
and having large round or oval conical depressions arranged
in linear series on opposite sides, from which spring aérial
roots; leaves acuminate with a median nerve.”
1870. Schimper. ‘Traité de paléontologie végétale, vol. ii.
p- 88.—Ulodendron (with which Bethrodendron is included)
is regarded by Schimper as a true genus. He believed that
the trunk in Ulodendron was simple or little branched as in
Sigillaria. He mentions that the leaf-scars, which somewhat
resemble those of Lepidodendron, remain almost of the same
size from the summit to the base of the stem, whereas in
Lepidodendron the leaf-scars gradually increase in size as we
recede from the summit to the base of the stem. The bark
of Ulodendron, on account of the thickening of the trunk,
seems to have become fissured instead of increasing in girth
with the growth of the stem. He accepts Lindley and
Hutton’s opinion, that the large Ulodendroid scars bore cones.
* For notes on this specimen, see next part of this article.
of Ulodendron to Lepidodendron, é&c. 133
In regard to the significance of these Ulodendroid scars he
says they are the result of an unequal dichotomy of the stem,
the alternate dichotomies being barren or fertile—the barren
going to form the axis of the stem, the other to form the
fertile branch, from which eventually results the Ulodendroid
sear. The tlong-lke impressions, which one almost always
notices, especially on the upper part of the large scars, he
ascribes to the impressions of the leaves at the base of the
fertile branch.
1871. Weiss. Fossile Flora der jiingsten Steinkohlen-
formation und des Rothliegenden im Saar-Rhein-Gebiete,
zweites Heft, p. 146.—This author does not express any
decided opinion on the relationship of Ulodendron to Lepido-
dendron, evidently preferring to leave the matter an open
question.
1872. Williamson. Philosophical Transactions, vol. clxii.
p- 209, pl. xxvi. fig. 24; pl. xxvii. figs. 25, 26; pl. xxviii.
figs. 27, 28.—The internal structure of Ulodendron is here
described by Dr. Williamson, who says: “ So far as all these
portions of its organization are concerned this Ulodendron
resembles the lowest type of Lepidodendron”’ (p. 210); and
again, ‘‘ It seems probable that these scars sustained objects
which were chiefly developed from the epidermal layer and
whose base rested upon the outer bark; they certainly were
not roots or branches, and I inchne to the belief that they
were organs of fructification.”
1875. Feistmantel. ‘‘ Versteinerungen der béhmischen
Kohlenablagerungen,” Paleontographica, vol. xxiii. p. 194.
—Feistmantel appears to have brought together in a confused
manner Lepidophloios, Lepidodendron, and Ulodendron. Under
Halonia punctata, L. & H. sp. (Bothrodendron punctatum,
L. & H.), is figured on pl. xlvi. a Ulodendroid stem, beneath
which is printed “‘ Halonia punctata, L.& H. Decorticated
state of Lepidodendron laricinum, Sternberg ;” but this plate
is also mentioned in the letterpress as an illustration of Lepi-
dophloios laricinus, Sternberg. On his pl. xlvi. is shown a
specimen of ‘‘ Ulodendron majus, Sternberg (?), probably only
a form of Lepidodendron.” ‘This plate is very roughly exe-
cuted, but from the form of the leaf-scars probably represents
Sigillaria discophora, Konig, sp. (=U. majus, L. & H.).
His pl. xlvii. may also belong to this species; but from the’
state of the preservation of the specimen, it is quite impossible
satisfactorily to settle the point.
1875-77. Stur. Culm Flora, pp. 262, 267, 270, and 283.
—Stur unites Ulodendron commutatum, Schimper (=U. par-
matum, Carruthers), with Lepidodendron Veltheimianum, and
134 Mr. R. Kidston on the Relationship
believes that the Ulodendroid scars bore detachable bulbils.
As to the organs which were attached to the large scars, he
draws into the discussion the figure of Lepidophlotos laricinus
given by Goldenberg in his ‘Flora Sarepontana fossilis,’
pl. xvi. tig. 6. Of this figure Stur says (p. 263): “ Golden-
berg has made known to us the under portion of the bulbils
of Lepidodendron. In the cited figure he has brought to our
knowledge a bulbil-bearing Lepidodendron-stem, under the
name of Lepidophloios laricinus, Sternberg.”
So far as immediately concerns Ulodendron, L. & H., the
figure of Lepidophloios laricinus given by Goldenberg and
referred to as above by Stur must be omitted from the dis-
cussion, for on no account can Lepidophloios be united with
Lepidodendron as now defined, or with Ulodendron as defined
by Lindley and Hutton—Lepidophloios forming, in fact, a very
distinct genus, which is separated from Lepidodendron by
well-marked characters, its leaves being attached to down-
ward directed cortical cushions whose leat-articulating surface
is placed at the lower extremity of the cushion, and is not
surrounded by a “field”? as in Lepidodendron*.
Ulodendron has two rows of large, depressed, oval or circular
scars, whereas the fruiting portion of Lepidophloios (Halo-
nia, L. & H.) has four or more rows of tubercles, which in
structure are also quite distinct from those of Ulodendron.
Therefore, when considering the affinities of the genus Ulo-
dendron, L. & H., the introduction of the genus Lepido-
phloios into the discussion can only further complicate the
subject, as Lepidodendron, Sigillaria, and Ulodendron are
essentially distinct, generically, from Lepidophloios. ‘The
statement made by Stur (p. 870), “that the bulbil-buds do
not in all Lepidodendra occur exactly in two rows, but may
also occur on the stem in more rows, the above-mentioned
figure of Goldenberg proves, on which the bulbils are arranged
in four rows,” appears to be founded ona misconception of the
true generic characters of Lepidodendron.
1880. Schimper, in Zittel and Schimper’s ‘ Handbuch der
Paldontologie,’ Band u. Lief. 1. p. 191.—The views men-
tioned in this work by Schimper are similar to those stated
in his ‘ Traité de paléontologie végétale.’ He recapitulates
the evidence on which he has founded his opinion that the
Ulodendroid scars mark the position of abortive branches,
resulting from unequal dichotomy, and which have been modi-
fied for the purpose of fructification, in a similar manner to
* See fig. 7, Pl. IV., and figs. 14 and 15, Pl. VIL, and explanations of
these figs. in Explanation of Plates.
of Ulodendron to Lepidodendron, de. 135
that which occurs in recent Lycopods, where the little cones
are only modified branches. These modified branches, he
believes, resulted in the formation of short-stalked cones; and
he mentions the following objections to Stur’s opinion that
the appendicular organs were detachable bulbils :—1st, that
when bulbils occur in the Lycopodiacee they are axillary, and
when shed leave behind them no scar on the branch ; and 2nd,
that they never show the regularity in position that is shown
in the scars of Ulodendron. Schimper here still regards
Ulodendron as a true genus, and appears to think that the
union of Ulodendron and Lepidodendron remains to be proved.
He admits that Lepddodendra commonly occur with Uloden-
dra, but can be distinguished from the last-named genus by
their larger leaf-scars and the absence of the Ulodendroid
scars.
1880. Thomson, D’Arcy W. “ Notes on Ulodendron and
Halonia”’ (Trans. Edinb. Geol. Soc. vol. i. part 11. p. 341).
—This writer enters into a general discussion as to the affini-
ties and structure of these plants. ‘The conclusions he arrives
at are :—
“Ist. That the scars of Ulodendron and Halonia, though
unequally developed, have similar significance.
“2nd. That these scars were points of attachment for the
organs of fructification, and that these organs were cones or
spikes, thicker and probably shorter than those of Lepido-
dendron.
“3rd. That in Ulodendron the cone was attached only to
the central point of the scar ; that the rest of this areola was
originally covered with leaves after the fashion of the remain-
ing portions of the stem; but was subsequently moulded by
the process of growth on the lower surface of the cone.
“4th. That the oval form occasionally presented by the
scars of Ulodendron is in all cases the result of secondary
causes, and that this and the other slight modifications of shape
and surface-markings in the scars are valueless as specific dis-
tinctions.
“5th. That the leaves of Ulodendron were small, narrow,
lanceolate, and imbricate after the ordinary Lepidodendroid
type, and that both Halonta and Ulodendron branched by
repeated dichotomy in the usual characteristic manner.
“Winally, That Ulodendron and Halonia were closely
allied Lepidodendroid plants; that on presumptive evidence
Prof. Williamson’s suggestion may still be retained, viz. that
Ulodendron and the biserial ‘ Halonie’ may possibly repre-
sent portions of one and the same form; and that, in this
136 Mr. R. Kidston on the Relationship
case, the specimens denominated Halonia formed the ter-
minal or young branches of Uledendron’*.
1880. Zeiller. Végétaux fossiles du terrain houiller de la
France (extracted from vol. iv. De explication de la carte
géologique de la France, p. 114).—This botanist writes:
‘““At present several authors unite the Ulodendra to the
Lepidodendra; I cannot see my way to adopt this view, at
least in the case of U. majus and U. minus.” .... “I do
not pretend, however, that all the Lycopodiaceze with branches
provided with large circular depressions ought to be separated
from the genus Lepidodendron, and that we might not meet
with trunks of this genus presenting this peculiarity ; practi-
cally it existsin the genus Bothrodendron.” + .. . “I believe
in the justice of regarding the geuus Ulodendron as a special
genus, distinguished from Lepidodendron by the mode of
attachment of its leaves.”
1880. Lesquereux. Coal Flora of Pennsylvania, p. 397.—
This author practically adopts the views held by Schimper.
As to appendicular organs Lesquereux thinks that in some
cases they have been cones, in others ‘‘ bud-like excrescences.”
This latter opinion is chiefly based on his Ulodendron Mans-
jieldi (pl. Ixvu. fig. 2), which, I think, may perhaps not
belong to Lindley and Hutton’s genus Ulodendron.
1882. Renault. Cours de botanique fossile, deuxiéme
année, p. 49.—Ulodendron is by this author treated as a
true genus. He says: ‘‘ Often a portion of the surface of
these disks [Ulodendroid scars] is covered by the foliar cica-
trices, a continuation of those of the trunk, but becoming a
little smaller ; it is necessary, then, that these disks should be
understood as the flattened remains of a conical fleshy mamelon,
of which the surface in continuation of that of the stem would
have been covered with similar but smaller leaves. At the
centre of the mamelon had been the axis of a caducous cone,
of which the traces are indicated by the central umbilicus ;
the considerable number of vascular bundles which converge
towards this part indicates a vegetative activity not in ac-
cordance with an abortive branch, but only with an axis,
destined to bear organs of reproduction.
“* ‘We have separated from this genus, which is characterized
by the form of the foliar cicatrices and by its biserial disks, two
* It is now conclusively known that ‘‘ Halonia” is the fruiting branch
of Lepidophloios ; hence it cannot possibly be “ terminal or young branches
of Ulodendron.”
+ The plants placed in Bothrodendron by Zeiller are not similar to
those included in Bothrodendron by Lindley and Hutton ; but this point
will be spoken of more fully presently.
of Ulodendron to Lepidodendron, é&c. 137
forms, of which the one corresponds to Lepidodendron Vel-
theimianum, the other to Lepidophloios laricinus, and that
because of their foliar cicatrices. We also separate for the
same reasons the following species— Ulodendron commutatum,
Schimper.” .... ‘ For our own part we regard Ulo. com-
mutatum as identical with the strobiliferous trunks of Lepido-
dendron Veltheimianum of Stur, and as not requiring to be
distinguished from it.” ....
Renault appears to be mistaken in the views he holds
of the relationships of Lepidodendron Veltheimianum and
Lepidophloios laricinus to each other. Had he examined
well-preserved specimens of Lepedodendron Veltheimianum
in the Ulodendroid condition it seems impossible to imagine
how Renault could have given such a figure of a “stem of
Lepidophloios restored in part” as that shown at fig. 1 of his
pl. x1. He says of this figure that it “ represents a fragment
of a trunk from the Coal-measures of Hschweiler and shows
on its surface the characteristic cicatrices of Lepidophloios
laricinus, but a little smaller.” This description, I am afraid,
is drawn up from the “ figure in part restored’ and not from
the specimen. In the copy of Goldenberg’s figure of Lepido-
phloios laricinus given by Renault on pl. ix. fig. 1, the
articulating surface of the leaf is represented at the upper end
of the cushion, its position being reversed from that repre-
sented by Goldenberg. ‘This alteration in the figure on the
part of Renault is erroneous, for most undoubtedly Golden-
berg has drawn his plant correctly, and the same arrangement
—a downward imbricating of the leaf-cushions—occurs also
in Lepidophloios scoticus, Kidston*.
But to enable one to accept the view that two forms of
leaf-scars occur in Lepidodendron Veltheimianum, one of the
normal form and the other having a Lepidophloios-like leaf-
sear, if Goldenberg’s figure of Lepidophloios laricinus is to
give any support to this opinion, it must be presumed that
fig. 1, pl. xvi. of the ‘ Flora Sareepontana fossilis’ represents
the leaf-scars turned upside down. ‘This is, however, not the
caset. In fact, in the Ulodendroid condition of Lepidoden-
dron Veltheimianum there do not exist two types of leaf-
scars, but only the ordinary Lepidodendroid type; the ap-
pearance which has given rise to this mistaken view in regard
to the Ulodendroid condition of Lepidodendron Veltheimia-
num will be referred to again more fully {. Suffice it to say
* See figure of this plant given under name of Lepidophivios laricinus
by Dr. Macfarlane (Trans. Edinb. Bot. Soe. vol. xiv. pl. vii.).
+ See Weiss, Foss. Flora d. jiing. Stk. u. d. Rothl. p. 154.
{ See the following part of this article.
138 Mr. R. Kidston on Ulodendron.
that the sketch given by Renault on pl. xi. fig. 1, which
shows three Ulodendroid scars placed on a stem bearing
Lepidophlovos \eaf-scars, represented in inverse position, does
not agree with any specimen which has come under my
notice either in nature or in the literature of fossil botany.
Most authors have united Dothrodendron, Lindley and
Hutton, with Ulodendron, and in this view I quite concur.
Some of the figures which accompany these notes show on
one or more parts of their surface a condition similar to that
upon which Lindley and Hutton founded their genus Bothro-
dendron*. There are, however, some recent writers who still
regard Bothrodendron as a true genus; to this view I must
therefore shortly refer.
1880. Zeiller. Wégétaux fossiles du terrain houiller de la
France, p. 116.—Bothrodendron is thus defined by Zeiller:
‘“Trunks marked with extremely small foliar cicatrices,
rhomboidal in form, rounded at the angles, placed in quin-
cuncial order, and each surmounted by a small cicatricule,
corresponding probably to the insertion of a scale. Foliar
cicatrices provided with three cicatricules, the central cica-
tricule placed slightly above the one on each side of it. The
large trunks present, in addition, large circular depressions,
more or less deeply concave and placed in two diametrically
opposite vertical rows.”
In Bothrodendron Zeller mentions two species—one B.
punctatum, L. & H., and the other B. (Ihytidodendron)
minutifolium, Boulay, sp. ‘This last-mentioned plant was
described by Boulay as a typé of a new genus which he calls
Rhytidodendront. ‘This genus,” Boulay says, ‘is charac-
terized in the group of the arborescent Lepidodendrez by the
very distant, transversely elliptical, and very small leat-scars,
which form a small area with three cicatricules surrounded by
an elevated border. ‘These three cicatricules at once separate
this genus from Stegmaria; the bark is delicate and finely
wrinkled and chagrined transversely ; after the decay of the
bark we find on the trunk two elongated prominences corre-
sponding to the cicatricules.”
In his ‘ Végét. foss. du terr. houil.,’ Zeiller does not give a
figure of the specimen he places under Bothrodendron puncta-
tum, L. & H.; but in his paper “ Observations sur quelques
cuticules”’{, under the name of B. punctatum, on pl. ix. fig. 1,
* See Pl. VI. fig. 10, da; Pl. VII. fig. 18, 8.
+ ‘Le terrain houiller du nord de la France et ses végétaux fossiles,’
p. 89 (1876). Lille.
{ Ann. des Sci. Nat. 6° sér. Bot. vol. xiii. p. 218, pl. ix. fig. 1.
Bibliographical Notice. 139
he illustrates a specimen which agrees with his description in
the work quoted. This figure and Boulay’s Rhytidodendron
minutifolium are justly placed in one genus by Zeiller; but
my friend has evidently mistaken the true character of Lindley
and Hutton’s genus Bothrodendron. It 1s true that Lindley
and Hutton, in the description of the two plates of Bothro-
dendron punctatum(Foss. Flora, pls. 1xxx., 1xxxi.), head their
description to pl. Ixxx. as ‘‘ corticated,” and, no doubt, this has
misled Zeiller in the identification of the fossil he has named
B. punctatum ; still, in the description Lindley and Hutton say,
“* Upon the surface of the stem are discoverable a considerable
number of minute dots, arranged in quincuncial manner, some-
thing less than half an inch apart, and itis probable that these
may be the scars of leaves; but at present there ts nothing to prove
that they were so.” It has since been proved that the little
“dots” which Lindley and Hutton thought might prove to be
leaf-scars, only mark the channels, on decorticated specimens,
through which the foliar vascular bundles passed to the leaves.
The types of Bothrodendron are now lost, but in the ‘“ Hutton
collection” are several specimens of the so-called Bothro-
dendron, all of which are undoubtedly decorticated specimens
of their Ulodendron majus or U. minus. Zeiller’s Bothro-
dendron punctatum must therefore be placed in Boulay’s
genus LRhytidodendron, and not Rhytidodendron united with
Bothrodendron, L. & H.
1882. Renault. Cours de botanique fossile, deuxigme
année, p. 51.—Bothrodendron is here also classed as a true
genus, and Renault embodies, in fact, the description given of
it by Zeiller. But Renault also treats Rhytidodendron, Boulay,
as a distinct genus, and places it after Bothrodendron. I
am quite of opinion that Rhytidodendron must be retained
as a distinct genus, and in it must be placed Bothrodendron,
Zeiller, but not Bothrodendron, Lindley and Hutton.
| To be continued. ]
BIBLIOGRAPHICAL NOTICE.
Year-Book of the Scientific and Learned Societies of Great Britain
and Ireland ; comprising Lists of the Papers read during 1884
before Societies engaged in fourteen Departments of Research, with
the Names of the Authors. Compiled from Official Sources.
Second Annual Issue. 8vo. London: Charles Griffin & Oo.,
1885.
Tur number of Societies dealing with scientific matters, and espe-
cially with subjects of Natural History, has of late years become so
great, and so many of the smaller ones, among a number of articles
140 Dublin Microscopical Club.
of merely local interest, publish from time to time papers of more
or less value, that it becomes a matter of considerable difficulty for
the working naturalist to know what has been done upon any
subject that may come before him. From this point of view the
‘Year-Book of Scientific and Learned Societies,’ of which the
second issue is now before us, is a publication of considerable
importance, and we can only hope that it may receive sufficient
patronage to justify the publishers in continuing its production.
This second issue forms an octavo volume of 230 pages, and con-
tains a list of societies, institutions, associations, clubs, and other
similar bodies established for the cultivation of science, and including
also some which hardly come under that denomination in the ordi-
nary sense, being devoted to the study of agriculture and horti-
culture, law, literature and history, and medicine. By far the
greater part of the bodies referred to, however, fall more or less
strictly under the category of scientific societies, and of these we
find detailed not only the titles and addresses, with generally the
names of the presidents and other officers, but also complete lists of
the papers read at their meetings during the year 1884, of the
doings in which this second *‘ year-book” is a record. The societies
referred to in the volume are classified under fourteen heads, so as
to bring together those which are established to perform similar
functions, or to deal with the same or allied branches of knowledge,
while the reference to any particular body is facilitated by the
addition of a copious index arranged alphabetically.
PROCEEDINGS OF LEARNED SOCIETIES.
DUBLIN MICROSCOPICAL CLUB.
April 24, 1884.
Section of Schorliferous Quartz.—Prof. V. Ball showed a section
of schorliferous quartz containing minute cells lined with a mineral
dendritically arranged, possibly manganese.
Technitella legumen new to Irish Waters.—Prof. Haddon showed
specimens of Technitella legumen (A. M. Norman) collected by Mr.
Charles Elcock in the Irish Sea, near the Isle of Man ; the first time
it has been found in Irish waters.
Corynium Beyerincki, a Fungus causing the “gumming” of
Cherries.—Mr. Greenwood Pim showed Corynium Beijerinckii, a
fungus said to be the cause of the gumming of cherries and other
fruit-trees, other species producing ‘“‘ gum tragacanth ” and similar
products. The plant consists of a darkish, jointed, rather knotty
mycelium, which produces 3—4-septate spores, broadly fusiform and
somewhat constricted at the joints.
Dublin Microscopical Club. 141
Gelatine Jelly simulating the “canal-system” of Hozoon canadense.
—Prof. Sollas showed a thin slice of gelatine jelly containing
groups of canals which curiously simulated in form, dimensions,
and arrangement the canal-system of Hozoon canadense. They were
obtained by slicing jelly frozen in Rutherford’s microtome, and
were no doubt caused by the crystallization of the water contained
in the jelly into spicules of ice, which, afterwards thawing, left tne
canalicular spaces exhibited.
Parasitic Structure on Moss-leaves—Mr. Archer showed leaves of a
moss, which he owed to Mr. EH. Parfitt of Exeter, bearing examples of
what appeared to be either a form of adventitious bud or a true
parasite growing on the edges and elsewhere from one of the leaf-cells.
This growth formed a short, stout, cylindrical “ filament,” thick-
walled and divided by four or five transverse septa, not obliquely
sloped, as in protonematous growths. The cells, thus much shorter
than broad, so formed were densely filled with coarse and scattered
chlorophyll granules. Thus their growth presented at first glance
a resemblance to some parasitic stigonematous algal form; but be
it parasite or not, it certainly seemed that it could not be of that
nature. It really seemed to be initiated by an outgrowth from one
of the constituent cells of the leaf, and then the short stout fila-
ment, as described, formed by further transverse division; but its
nature or purport remained a question.
Structure of Stem of Draccena reflewa.—Prof. M‘Nab showed a
transverse section of the stem of Dracena reflexa, showing circum-
ferential growth by means of a meristem layer, which is to be
regarded probably as the homologue of the interfascicular cambium of
the dicotyledon, and that while the cambium of the dicotyledon
gives rise to new wood, new bast, and new ground-tissue (medullary
rays), the meristem gives rise in the tree Liliacese to the libero-
ligneous bundles and ground-tissue.
May 15, 1884.
Pezxza postuma from Potato-stalks—Mr. Greenwood Pim showed
Peziza postuma (Berk. et Wilson) growing from the sclerotia of
potato-stalks, and which corresponded to the figures by Mr. Wilson
in the ‘ Gardeners’ Chronicle.’ The whole plant in situ was exhi-
bited, as well as a section under the microscope, showing sporidia
&c. Mr. Pim had shown sections of the sclerotium to the Club a
couple of years previously. The fully-developed Peziza from fruit
was observed by Mr. Wilson in 1883. Mr. Pim’s specimens were
grown in damp Sphagnum in his greenhouse. He was indebted
for the sclerotia to the kindness of Mr. Carroll, of the Model Farm,
Glasnevin, who had received large quantities from various parts of
Ireland, where last year it proved a formidable form of disease, quite
distinct, of course, from the ordinary potato-murrain.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. il;
142 Dublin Microseopical Club.
Section from Calf’s Stomach.—Prof. Cunningham showed a sec-
tion from a ealf’s stomach displaying the villi.
Presumed new Heliozoon discovered by Mr. Bolton near Bur-
mingham.—Mr. Archer showed a sample from a gathering kindly
forwarded to him by Mr. Bolton. of Birmingham, announced to
contain a new and minute form of Hehozoon ; but after a careful
search through the material he had failed to find anything living, at
all coming up to the expectation formed from Mr. Bolton’s accom-
panying description. He had, however, met with, and now drew
attention to, an organism which might, casually viewed, be regarded
as a Heliozoon; but whatever might be the real nature of this, it
could not be set down as appertaining to that group. This was
globular, rather less than ;,),, inch im diameter, contents green,
and rather thick-walled, and it was outwardly beset with nume-
rous short, indistinct, subtruncate, subpellucid papille. Thus its
radiate or stellate aspect lent this organism a certain amount of
deceptive resemblance to a Heliozoon; but it could not be the
organism referred to by Mr. Bolton, as it only distantly resembled:
his drawing. The gathering contained a quantity of Huglene
passing into a vegetative condition by repeated self-division, and the
conjecture presented itself, Might this globose papilliferous body
represent an ultimate state of division of a Huglena, passed now
into a globular thick-walled subspinulose resting form? But there
was, further, in the gathering now and again to be detected an
empty cell-wall, very thin, very hyaline, of a globular figure, and
bearing a number of longish setz or bristle-like hyaline spines, not
unlike, only that these were notably more numerous, an empty skin
of an example of the alga Mr. Archer had on a former occasion
brought before the Club as Oocystis sctigera. This too had the
outline of a Heliozoon, but no sarcodic contents with green chloro-
phyll-bodies within, as depicted in the sketches, were present, and
the longish bristle-like radii were clearly not pseudopodia, but rigid
sete. Here, then, was yet another object that might be taken at
first glance for a Heliozoon, but it was obviously merely an empty
cell-wall of great tenuity, not a globose sarcodic mass, however
pellucid. It will be seen that it might be rather the evacuated
cell-wall of some spore, to a certain extent of course calling to
mind the zygospore of some Desmidian like Staurustrum dejectum,
&e.; but it was, on the other hand, much more thin-walled and
the radii were more slender and delicate than the empty cell-wall of
such a zygospore, viewed under the same power, would appear to be.
He had therefore missed what Mr. Bolton wished him to see; but
it was nevertheless curious that, in so small an amount of material,
two seemingly distinct things, superficially somewhat mutually
alike, and both at the same time superficially like a minute Heliozoon,
and both apparently novel in themselves, should occur. Mr. Archer
really did know a minute Heliozoon, green, non-pulsating, with
very slender pseudopodia, the green granules rather small and
Dublin Microscopical Club. 143
somewhat densely filling up the mass—one to which he had never
drawn attention, as its characteristics were found very difficult to
determine ; but it seemed certain that neither of the organisms
here drawn attention to, nor, judging from Mr. Bolton’s sketches,
could his Heliozoon, be considered identical therewith.
Undescribed Epidermal Gland in Chiton.—Prof. Haddon exhi-
bited transverse sections of Chiton (Trachydermon) ruber (Linn.),
showing an undescribed epidermal gland at the posterior end of the
animal on each side beyond the gills, which it is proposed to call
the fenestral gland.
Development of Spicules in Geodia Barretti.—Prof. Sollas showed
slices of Geodia Barretti in which the development of the globular
spicules within a mother-cell could be traced threugh all the
stages.
Ceil-division im a problematic Chroococeaceous Alga.—Prof. M‘Nab
exhibited a slide of the Chroococeaceous alga from the wall of the
stove at Glasnevin which contained the Desmids formerly exhibited.
The material had been kept for about twelve months in a corked
bottle, and the cells were dividing first into two and two, that is
four cells placed linearly, and next into two transversely, so as to
form two rows of four cells: all the cells remained in the gelatinous
investment. The result of the division was the formation of eight
very minute cells, whose further development was still under obser-
vation.
June 19, 1884.
Torrubia militaris new to Ireland—Mr. Pim showed a section
through the receptacle of Torrubia militaris which he had recently
found growing (as is usual) from the body of a grub in Powerscourt
demesne, near the Waterfall, being its first record, as far as he
knew,in Ireland. The long and flexuous asci containing filiform
sporidia are very striking.
Alcyonella fungosa exhibited —Prof. Haddon exhibited Aleyonella
fungosa in a living condition.
Archerina Boltoni, Lankester, exhibited in a living condition.—
Mr. Archer presented for examination a group of four individuals of
the new Sarcodine discovered by Mr. Bolton, of Birmingham, a
specimen of which he had failed to find in the former gathering
shown to the Club at last meeting. Here it was now “in the
flesh,” and a veritable novelty, which Prof. Lankester had done
Mr. Archer and Mr. Bolton jointly the honour to designate, at least
pro tempore, as Archerina Boltoni. As the group now under view
showed, this is a more or less gregarious form, extremely minute
se
144 Dublin Microscopical Club.
(say about ;~4,, inch in diameter), orbicular, pellucid, containing
one or two large chlorophyll-corpuscles, of elongate, somewhat
-kidney-shaped figure and smooth outline, and seemingly homo-
geneous texture, lying up against the periphery, thus leaving the
centre more or less clear; the pseudopodia radiating in every diree-
tion, not very numerous, straight, very slender, long (say twice,
thrice, or four times the diameter of the spherical body-mass),
hyaline, clear; the outline of the body-mass sharp and smooth,
not showing any pulsating vacuoles, nor allowing any nucleus
to be detected. If a nucleus were present it might be supposed
to be readily enough perceived in a body so clear as this, for
even (now that we know that it is there) in the comparatively
opaque and granuliferous body of <Actinophrys sol, in certain
exumples, he thought it was not very difficult to detect the
presence of the nucleus, even without dyeing. But the examples of
this new form in the gathering were so few and far between, Mr.
Archer had had no opportunity of experimenting to test the exis-
tence of a nucleus. No doubt the habit and appearance of this
very minute form was that of a Heliozoon; but had it really no
nucleus, what would it really be? Again, could it be possible that
the very hyaline pellicular exuvium shown at last meeting has any-
thing really after all to say to this organism? Could it be really
possible that on becoming encysted it did not withdraw the pseudo-
podia, but beeame coated (body, pseudopodia, and all) in such a
spinulose filmy envelope as that drawn attention to at the last
meeting? If so, when the living protoplasmic substance withdraws
therefrom, so as to leave behind the “ spore-like” spinulose exu-
vium, the pseudopodia must pull themselves out of their minute
tubular investments, and then escape (by a rent ?) from the central
globular portion. Is this pellucid integument composed of cellu-
lose? All this would be very remarkable, and seems to indicate that
this organism is at least most probably not a Heliozoon, much as it
simulates one, but a Sarcodine of “‘ lower” type. It is possible the
great sharply-defined chlorophyll-masses might at some epoch
become “ zoospores” and perhaps “conjugate ;” but this is only
supposition. Mr. Archer learnt that Prof. Lankester was making a
thorough examination with large material of this form, and it was
to be hoped that he might be able to throw much light upon it. One
thing at least was certain, that this was not the same green “ Helio-
zoon”’ referred to by Mr. Archer at last meeting. At any rate,
this is undoubtedly a new form ; and Mr. Archer felt greatly indebted,
so far as he was concerned, to Prof. Lankester for the honour done
him in connecting his name with so interesting a novelty. He had
also to thank Mr. Bolton very much for his courtesy and the pains
he had taken to cause him at last to see the right thing.
A modified Microtome exhibited —Dr. Scott exhibited a microtome
devised by Dr. Hayes, Merrion Square, mainly on the model of the
instrument by Junge of Heidelberg ; but in place of the very great
Dublin Microscopical Club. 145
delicacy which characterizes that instrument, this one was made
rather roughly and strongly, rendering it more suitable for ordinary
use. In place of a costly knife, of peculiar pattern, it worked with
an ordinary razor, and was adapted for freezing tissues by means of
ether. By a simple arrangement which Dr. Scott fitted to it, con-
tinuous series of sections of known thickness could be cut with ease.
The price was also exceptionally low.
Chert with Sponge-spicules.—Prof. Sollas showed sections of chert
from Lias with sponge-spicules.
Experiments to alustrate the Application of the Microscope to
practical Mineralogical Questions, were shown by Prof. Tichborne.
In examining an argentiferous mineral which was found in Wales,
and known thereas “blue stone,” it became desirable to determine
- whether the said mineral was a definite double sulphide of lead and
zinc, or whether it was a fine mechanical mixture of the two weil-
known minerals galena and blende. The said blue stone had been also
found in Ireland at Ovoca, and being considered a definite mineral,
had been christened Killmacooite, from alocalname. Dr. Tichborne
found that on gradually powdering the mineral and examining it
' from time to time under the microscope, a point was at length reached
when half the particles became transparent and transmitted light,
whilst no amount of powdering would render the other particles
transparent. ‘T’o try such an experiment it was necessary to view
with very strong transmitted light (a half-inch object-glass) and
to cut off all reflected light. From this experiment he came to the
conclusion that the mineral was an intimate mixture of fine crystals
of blende and galena, the blende being the transparent particles and
the galena the opaque. Although both these minerals possess a certain
degree of metallic lustre, galena is one of the most perfectly opaque
substances known, whilst blende in very thin layers is perfectly
transparent. Prof. Tichborne illustrated this by depositing thin
layers of artificial galena and blende upon glass by the action of
sulpho-urea upon alkaline solutions of the respective oxides of lead
and zine.
October 16, 1884.
Structure of Leaves of Abies subalpina, Engelm.— Prof. M‘Nab ex-
hibited sections of leaves of Abzes subalpina, Engelmann, which he
had collected in Kicking Horse Pass, Rocky Mountains, Sept. 12,
1884. These differed in no way from leaves of the type specimen
of Abies lasiocarpa, Hooker, a species sent by Douglas from the
very same region, and thus, according to the strict law of priority,
Engelmann’s recent name should be rejected.
Zygospore of Cosmarium cucurbita.—Mr. Archer showed the zygo-
spore, or what appeared to be the zygospore, of Cosinarium cucur-
bita, collected by Mr. Pim at Killarney a few weeks previously.
This formed a somewhat elongate, on the whole subelliptic figure,
146 Dublin Microscopical Club.
the surface elevated into a number (say probably ten or twelve) of
large hemispherical prominences ; thus the whole presented a very
broadly undulate outline. The cell-wall was thick, destitute of any
processes beyond the somewhat tall rounded prominences, as men-
tioned. The chlorophyll-contents dense and remaining of a bright
green. The identification of this pretty object as the zygospore of
the species mentioned rested upon the presence of a pair of empty
semicells, seemingly involved with it, and in just the position they
ought to assume if they really were the halves of one of the parent-
cells; of course this assumption would have been enormously forti-
fied, if not indeed absolutely determined, had the empty semicells
of another parent-cell been found in a corresponding position. At
any rate, there could be but little doubt that this really was a
spore ; and if the assumption as to its identity be correct, this would
seem to be the first record of the zygospore of that very common -
species. Indeed it is rather curious how rarely some of the common
species of Desmidiew are met with conjugated, though others, indeed,
are frequently so encountered. The present zygospore has little
resemblance to any other, and at least could not be mistaken seem-
ingly for any described. Perhaps of all forms known it had most
resemblance to that of Penium phymatosporum, a not uncommon .
species, of which, however, Mr. Archer had only once seen the
zygospore ; but, as might be expected from the relative size of the
species, the present zygospore is far smaller, and, though seem-
ingly elongate, is not subquadrate and compressed ; it is, as men-
tioned, in general form elliptic, and might be described as broadly
undulato-ovate. It has a certain resemblance, too, to the zygospore
of one at least of three common forms, confused under the name
Cosmarium margaritiferum, which, however, is greatly larger,
spherical, and its hemispherical prominences, in proportion to the
bulk of the total mass of the zygospore, not nearly so elevated.
Gelatinous Alga from a Geyser-basin, Yellowstone Park, Wye-
ming.—Mr. G. F. Fitzgerald exhibited some morsels of a gelatinous
growth which he had found in the “ Prismatic Pool” in the middle
of a Geyser-basin, Yellowstone Park, Wyoming, United States.
The mass from which he had taken the specimens grew to a distance
of about 5 or 6 feet nearly all round the edge of the pool, which was
about 30 yardsin diameter. The water of the pool overflowed its edge
almost throughout, and it was in this overflow water that the jelly-
like substance grew. The temperature of the water was from 100°
to120°Fahr. It grew on what appeared to be a flat tuffa rock, depo-
sited out of the water of the pool, and covered it very uniformly to a
depth of about an inch to an inch anda half. Its upper surface
was somewhat lumpy, very much like the thick moss that grows in
cushions on the tops of walls, when the cushions get close enough to
make a continuous surface. The upper surface was bright red,
but below it was a nearly clear jelly of about the consistency
Dublin Microscopical Club. 147
of a slimy stiff calf’s-foot jelly. Under the top surface there were
a series of what appeared like surfaces of growth that gave a vertical
section somewhat the appearance of some agates.
November 20, 1884.
Canadian Specimen of Cosmarium notabile, Bréb.—Mr. Archer
drew attention to specimens of Cosmariwm notabile, Bréb., a rather
small form, found in a Canadian gathering made by Prof. M‘Nab on
his recent visit. This is far from a common species here at home,
but can hardly be called a rarity. It seems to be a constant form,
though differing slightly in dimensions. Very few other forms
occurred in the Canadian gathering, and none seemingly very note-
worthy. A Palmellaceous algal form occurred in the gathering, of
which Dr. M‘Nab showed a slide. Some of the examples presented
the appearance of a slipping out of the proteplasmic contents of
certain of the cells en masse; some seemingly showing this pheno-
menon in a more remarkable manner Mr. Archer had met with
in some of the material Dr. M‘Nab had given him.
Nostoc calidarium, Wood, from Geyser-basin, Wyoming.—Dr. EK.
Perceval Wright showed a few mounted fragments of the gelatinous
alga from the Geyser-basin, Yellowstone Park, Wyoming, which had
been collected by Mr. G. F. Fitzgerald, and exhibited at the previous
meeting of the Club. The mass seemed to be composed of a mat-
ting together of several algal forms, the prominent species in which
was a Wostoc, very possibly Nostoe calidariwm, Wood, a species
described as found in a thermal spring in the northern portion of
Owen’s Valley, California, the temperature of the water being be-
tween 110° and 120° Fahr., or about the same as that of the water
in which the specimens exhibited vegetated. Although the two
sets of filaments referred to by Wood were present in the mass,
no heterocysts had been detected. The other forms found were a
Chroococcus, pretty generally diffused, and much more sparsely an
Oscillatoria, provisionally O. Frohlichit.
Aregma (Phragmidium) obtusum, Link, exhibited—Mr. Green-
wood Pim showed Aregma (Phragmidium) obtusum, Link, which
occurred on leaves of the “ Barren Strawberry” (Potentilla fraga-
riastrum), in Hollybrook, near Bray, last autumn. This form is
very distinct from those occurring on the bramble, rose, and rasp-
berry, one of which was shown for comparison, in being quite obtuse
at the apex of the spore and haying a very short stalk. It appears
rare, this being its first notice in Ireland, but occurring on a small
and insignificant plant may probably often escape detection. It is
curious that the three closely allied genera Aregma, Xenodochus, and
Triphragmium are confined to members of the natural order Rosacee,
whilst the extensive series of Puccinias, also nearly related, are
found on various natural orders, Rosacee being almost exempt.
148 Dublin Microscopical Club.
Myliusia Grayi.—Octahedral nodes of the skeleton, in compa-
rison with those of Dactylocalyw pumiceus in the young state, were
shown by Prof. Sollas.
Cienodrilus, sp., a living example, was shown by Prof. Haddon.
December 18, 1884.
Plant-remains from Silurian Rocks.—Prof. Sollas showed a sec-
tion from Silurian rocks presenting what seemed to be plant-
remains, forming, in a longitudinal view, long drawn out, large, and
thick-walled, variously sized non-septate tubes, and in a transverse
view presenting each a circular outline, these involved in a common
matrix.
Section of Quartz-trachyte, or Liparite, from the Neighbourhood of
Smyrna, was shown by Prof. Hull, F.R.S. The district is well
known to be rich in volcanic rocks of Tertiary age, consisting of
trachytic, augitic, and other varieties of rock, together with tuffs and
agelomerates, on a mass of which last the ancient castle is built.
The section exhibited is taken from a grey porphyritic rock, con-
taining numerous crystals of sanidine, plagioclase, minute grains
of quartz, crystals of biotite, augite, hornblende ?, sub-crystalline
forms of vesuvian, and magnetite in small quantity in octahedral
grains—in all about eight varieties of minerals set in a “ ground-
mass ” (or paste) of glass.
The ground-mass requires a rather high power for observation,
and is seen to consist of a glass traversed by multitudes of trichites
and microliths, together with minute colourless prisms of apatite,
quartz grains, and crystals of plagioclase. The quartz grains, both
large and small, are also seen to contain numerous cavities, some
with fluid, some containing “ dust” or specks of magnetite (?),
From the above account it will be inferred that, with the polari-
scope, the section offers a very beautiful appearance, the various
minerals displaying their coloration with ever varying effects as the
polarizer is made to rotate.
On the whole it would appear that the rock answers pretty well
to the description of “ Liparite” of Roth, as given by Zirkel
(‘Mineralien und Gesteine,’ p. 345) and Rosenbusch (‘ Mikro-
scopische Physiographie d. Mineralien, Band u. p. 188).
Remarkable Spore or Spore-like Body from the Carboniferous For-
mation.—Prof, Haddon exhibited a spore or spore-like body found in
a section from the Carboniferous formation, Halifax, forming a very
pretty object, much resembling some desmidian zygospore in its orbi-
cular figure, beset all over by numerous short processes of equal
length, causing the whole to present a stellate aspect.
Spheroblasts from Stem of Privet (Ligustrum vulgare).—Dr.
M‘Nab exhibited a section of an arrested bud from the stem of
Geological Society. 149
the privet (Ligustrum vulgare), the specimens of which were sent to
him by Mr. Greenwood Pim. ‘The arrested buds were numerous on
the stem and were not arranged in any special order, so that there
were probably both normal and adventitious buds, converted into
spheroblasts, ike those so well known on the stem of the beech.
Two peculiarities were noticeable: first, that the sides of the bud
had four rows of leaf-scars, all internodes having been suppressed ;
and second, some of the arrested buds had produced opposite lateral
buds, right and left, at their base, thus forming a three-lobed struc-
ture. The transverse section, shown under the microscope, ex-
hibited a very remarkable contorted condition of the wood, with
only slight traces externally of medullary rays. Both pith and
cortex were well developed. The vessels were few and small, and
the whole appearance was very different from that of normal privet-
“wood.
Photographs of Diatoms exhibited.—Prof. Haddon showed some
fine photographs of Diatoms, from the War Museum, Washington,
made under a very large amplification (2000-3000 diam.) of great
beauty and clearness.
Prof. EK. Perceval Wright showed examples and drawings of a
new genus and species of Alcyonaria from the ‘Challenger’ col-
lection.
Variety of * Grit” from Bray Head exhibited—Prof. V. Ball,
F.R.S., exhibited a section of a dense purple-coloured rock which is
found near the southern extremity of the section of Cambrian rocks
forming Bray Head. The mode of occurrence of this rock being for
the most part obscure, although at one point it is distinctly stratified,
this, together with its density and hardness, made it desirable to
examine its microscopical characters. It proves to be a distinctly
elastic rock, consisting mainly of small fragments of quartz in a
_ferruginous matrix. It may be regarded as a somewhat exceptional
variety of the class of rocks of this age to which the term “ grit”
used to be applied by Prof. Jukes.
GEOLOGICAL SOCIETY.
April 15, 1885.—Prof. T. G. Bonney, D.Sc., LL.D., F.R.S.,
President, in the Chair.
The following communication was read :—
“Notes on the Polyzoa and Foraminifera of the Cambridge
Greensand.” By G. RK. Vine, Esq. Communicated by Thomas
Jesson, Hsq., F.G.8.
After commenting on the want of published information con-
cerning the Polyzoa of the Cambridge Greensand, as shown by the
150 Miscellaneous.
fact that none are mentioned in Mr. Jukes-Browne’s list of the fossils
(Quart. Journ. Geol. Soc. xxxi. p. 305), the author proceeded to
explain the circumstances under which he had been entrusted with
the whole of Mr. T. Jesson’s collection from the coprolite-bed for
description. The collection is large and important, and the Polyzoa
contained exhibit a facies distinct from that of the Jurassic beds on
the one hand and of the Upper Chalk on the other. There is but
little similarity between the collection now described and the forms
known from Warminster and Farringdon. The majority of the
Cambridge-Greensand Polyzoa occurred unattached to any matrix ;
but several examples of attachment have been observed, chiefly to
Ostrea, Radiolites, and species of Cidaris.
A list showing the range of the species described preceded the
actual descriptions of the following kinds of Polyzoa and Forami-
nifera, with notes on their relations &c. It included :—
PoLyzoa.
Stomatopora gracilis, Milne-Hdw. Lichenopora, sp.
Idmonea dorsata, Hagencw. ? paucipora, Vine.
Entalophora raripora, D’ Orb. Dromopora stellata, Goldfuss.
Jessonii, sp. nov. polytaxis, Hagenow.
striatopora, sp. nov. Osculipora plebeia, Novall.
gigantopora, sp, Nov. Truncatula, sp.
Diastopora cretacea, Vine. Membranipora cantabrigiensis, sp.
, var. lineata, var. nov. nov.
fecunda, sp. nov. Microporella, sp. (? antiquata).
—— megalopora, sp. nov. Lunularia cretacea, Defr. & D’ Orb.
FoRAMINIFERA.
Webbina levis, Sodlas. Trochammina irregularis?, D’ Ord.
tubercnlata, Sollas. Textularia, sp.
MISCELLANEOUS.
On the Existence of a Nervous System in the Accelous Planarie and
of aw new Sense-organ in Convoluta Schultz. By M. Yves
DELAGE.
‘HERE are in the animal kingdom a small number of creatures with
differentiated tissues in which no neryous system has been recog-
nized. Nevertheless the well-known existence in them of sense-
organs almost enables us to assert @ priora that of ganglionic cells
and of nerves. Among these creatures are the lowest Planaric inclu-
ded in the group of the Accelous Rhabdoccela. In the most recent
and the most authoritative work upon this subject, that of L. Graff,
these Planariz are described as having no nervous system. Never-
theless a Russian zoologist, Mlle. Pereyaslawzew, speaking inciden-
Miscellaneous. 151
tally of the adult in a note treating of the development of the
embryo of the Accela, says :—‘‘ I have found the nervous system in
the adult Accela, as well as the digestive cavity, perfectly visible in
sections.” All our knowledge upon this subject is limited to this
phrase, which is not followed by any description or accompanied by
any figure.
In one of our most interesting Accela, Convoluta Schultz (O.
Schm.), I have discovered a very developed nervous system, and I
have been able to display it with the greatest distinctness, not only
in sections, but in the animal when entire.
Nervous System.—Around the otocyst we find a bilobate gangli-
onic mass, which forms the principal part of the central system.
Two other masses, forming a pair, smaller and situated higher up *,
are attached to the principal mass by two large connectives, and are
united to one another by a transverse commissure. ‘These central
parts of the nervous system are composed of fibres and cells. The
fibres occupy the centre of the dilated parts, and form almost the
whole of the connective and commissural cords. They are exceed-
ingly fine and delicate, undulated and parallel. The cells are situ-
ated at the periphery of the dilated parts, and form especially a great
ageregation at the postero-inferior part of the principal mass, and a
continuous layer around the otocyst. They are of an average
diameter of 5 p to 7 w, and are polyhedra]. In some of them one
can see starting from the angles processes which throw themselves
into the layer of fibres. Their single nucleus, which is not nucleo-
lated, is 3-4 y in diameter.
The peripheral system is formed by six parallel longitudinal
nerves and their ramifications. These nerves are situated immedi-
ately underneath the layer of zoochlorelle ; they form three ee
external one, which runs in the folded margins of the body ;
internal one, which descends a little beyond the median line ; wl
an intermediate one, situated at nearly equal distances between the
two preceding. These last two pairs correspond to the four clear
streaks which may be observed in the living animal without any
preparation. ‘The internal nerve on each side originates from the
principal ganglionic mass which surrounds the otocyst. The two
external nerves originate by a short, common, transverse trunk
from the small superior mass. A cord starting from the inferior
ganglion joins the median nerve at its origin, so that the latter has
a double origin. These longitudinal trunks are united by transverse
anastomoses, which cut them at right angles, like the rungs of a
ladder. These anastomoses are not all perfectly constant in their
position, but the variation is not considerable. In a general way
they become more and more numerous the further they are from the
head. At the inferior extremity the cords converge and resolve
* As usual I place the animal with the head upwards and the ventral
surface in front.
152 Miscellaneous.
themselves into a rich plexus. From the principal cords and from
the anastomoses issue numerous very fine filaments which anasto-
mose among themselves so as to form a network with square or
rectangular meshes. The nerves are composed of the same fine
fibres as the commissures of the central system.
Sense-organs.—Besides the otocyst, notwithstanding what Graff
has said, there exist two eyes, represented by two yellow pigment-
spots, and I have recognized the existence of a new sensitive appa-
ratus which I shall name the frontal organ. It is an ovoid, clear,
refringent mass, situated at the superior terminal extremity. It
measures about 0-04 millim. by 0:03 millim. The larger end of the
ovoid is situated at a small distance from the highest commissure of
the nervous system, or even reaches it; the smaller end is applied
against the integuments, which, at this level, are destitute of cilia
and furnished with short conical papille regularly arranged. The
mass is bounded at the sides by a double layer of ganglionic cells.
A small number of cells of the same kind exist in its interior.
From the bounding cells, the central cells, and the nervous commis-
sure start numerous very fine filaments which anastomose in the
refringent mass and form a network; then the filaments gradually
approach other and converge regularly towards the superior extre-
mity, where they terminate each in one of the papillz mentioned
above. In a great many cases I have been able to trace the fila-
ments from the cells in which they originate to the terminal papilla.
The refringent matter performs the function of a sustaining sub-
stance. Jhe whole apparatus is very mobile, and the animal seems
incessantly to feel about with the papillae which terminate it.
In young Convolute just hatched and still destitute of zoochlo-
rellee the frontal organ exists even more highly developed in propor-
tion than in the adults, and I have been able to demonstrate the
nervous system, which is constituted us in the adult, but less
condensed and less rich in ramifications.
Lacune of the Reticulum.—The nerves appear everywhere sur-
rounded by an endothelial sheath, the cells of which, smooth and
flattened on the side towards the nerve, are continuous externally
with those of the reticulum. The cavity included between the
nerve and its sheath is not entirely virtual. By means of a certain
reagent which I shall make known we can demonstrate the existence
of a cavity between the nerve and its sheath, and this cavity is
continuous throughout with a very highly developed system of
lacunee, which occupies the whole of the zvochlorella-layer. Each
of these Algz is enclosed in a free cavity, and the spaces interposed
between these cavities are formed by the lacunee in question. More
circumstantial details upon this point will be given in my forthcoming
memoir.
The German zoologists have reproached M. Blanchard with having
injected the nervous system of the Planariz, and described this
Miscellaneous. 153
nervous system as a circulatory apparatus. But a nervous system
is not a hollow organ capable of being injected, and the imputation
seems to have been made a little inconsiderately. The discussion
not having related to the Accela I do not know how far my results
may apply to the Planariz injected by M. Blanchard; but in alla
sheath seems to exist around the nerves, and if the contiguous
lacune also existed, we should have in them a natural explanation
of all the difficulties, and the proof that the mistake has not been
entirely on the side of the French zoologist.—Comptes Fons,
July 20, 1885, p. 256.
The Nest of the Fiftcen-spined Stickleback. By Prof. Kart Mosrvs.
Among the fishes of the Bay of Kiel the sea-stickleback (Spina-
chia vulgaris, Flem.) is distinguished by the remarkable instinct of
constructing a nest for its eggs and young. For this purpose it
employs delicate plants which grow in the shallow water, and masses
these upon Zostere or the fronds of seaweeds which wave below
the surface of the water or on the piles of landing-stages, until they
form a soft rounded mass of 5-8 centim. in diameter. In this nest
the female, in May or June, deposits several masses of ova, and the
male surrounds the nest with white silky threads and then keeps
watch by it.
All this has long been known, but exact knowledge of the con-
stitution of the threads and the place of their origin has hitherto
been wanting. The examination of male sea-sticklebacks in May
and June 1884, enables me to state that the threads are usually from
0-12 to 0°13 millim. in diameter, and consist of several cords stuck -
together, which, again, are composed of very fine parallel threads.
The substance of which they are composed is nitrogenous, and is a
peculiar modification of mucine, as appears from its behaviour to-
wards various acids and alkalies. It is formed in the kidneys of
the male, and, indeed, in the epithelial cells of the urinary canals,
which exert this form of activity only at the time of reproduction,
and during this period behave towards staining reagents in the same
way as the muciferous organs of other Vertebrata.
The kidneys of mucus-bearing sea-sticklebacks are inflated,
especially at their posterior extremity. From the kidneys the
mucus passes through the ureters into the bladder, which is thereby
dilated into a large pyriform vesicle, from the opening of which the
mucus finally oozes out as a white thread-forming mass and attaches
itself to solid objects that it touches. A male stickleback from the
urinary aperture of which mucus protrudes therefore needs only to
move around the nest in order to spin round the masses composing
it and the adherent ova.—Schriften naturwiss. Vereins fur Schleswig-
Holstein, Band vi. Heft 1, 1885.
154 Miscellaneous.
Freia ampulla, the Flask-Animalcule.
By Prof. Kart Mosrvs.
One of the largest and finest Infusoria of Kiel Bay is Freia
ampulla, O. F. Mill., the flask-animalcule. When full-grown and
completely extended it is nearly 1 millim. long and 0:1 millim.
broad, so that it is perceptible even with the naked eye. It resides
in a flask-shaped capsule with a convex bottom, a short neck, and
the margins of the aperture bent outward. This capsule is trans-
parent, brownish yellow or somewhat bluish, and consists of a chiti-
nous substance which is insoluble in potash. The greater part of
the extended animal is cylindrical. Its posterior extremity is
attached to the bottom of the capsule, while the anterior portion
can reach far beyond the aperture of the capsule, and is divided
into two lanceolate lobes, the bases of which are united to form a
half-funnel, in the bottom of which the mouth is situated. The
edge of these funnel-lobes is covered with combs of cilia or pecti-
nelle, the united bases of which cross the edge-line nearly at right
angles. The pectinella-fringes of the two funnel-lobes run spirally
down the funnel as far as the mouth.
When the animalcule has extended itself and separated the
funnel-lobes it sets a portion or the whole of its pectinellze in motion,
and thus produces currents which carry smaller Infusoria, unicellular
Alge, or granules of indigo or carmine mixed with the water into
the cavity of the mouth. When the latter is filled it opens inwards
and allows the food, in the form of a rounded ball, to pass into the
esophagus, which may be recognized as a longitudinally-striated
canal behind the mouth, in the middle of the fore part of the body.
From the cesophagus the food-balls pass into the soft endoswre of the
middle and hind body ; many food-balls are also pushed up forward
even into the endosare of the funnel-lobes. The indigestible parts
are expelled at the base of the left funnel-lobe. Several fixcal balls
usually collect to the lett of and somewhat behind the bottom of
the funnel, in a canal, a sort of rectum, and escape quickly one after
the other.
The soft endosare is covered with a firmer layer of ectosare,
which consists of long streaks beset with greenish-brown granules.
These streaks act like muscular fibres. When they contract, the
hind-body becomes thicker and applied to the bottom of the capsule,
while the fore-body with the funnel-lobesfolded together passes down
below the aperture of the capsule. Freia ampulla usually retracts
itself quickly into the capsule, and only slowly extends itself again.
In the middle and hinder parts of the body there is a light neck-
la¢e-like cord, which is coloured red by solution of carmine. This
is the nucleus.
In many capsules there is, at the side of the hind-body of a per-
fectly developed individual, a young animal without funnel-lobes,
nearly uniformly rounded off anteriorly and posteriorly, and pro-
duced by fission from the body of the parent animal. This, when it
Miscellaneous. 155
is still connected with its parent only by a slender cord, stretches
the fore part of the body out of the capsule, tears itself free, and
swims away, carried along by fine cilia which cover the whole body
in close longitudinal series. At the anterior extremity rudiments
of pectinelle already show themselves, and a slight notch is the
beginning of the formation of the funnel-lobes. After the young
animal has swum about freely for a time it attaches itself to some
firm support and secretes the material of the capsule as a trans-
parent mass, thicker behind than before, where it is not yet turned
out as in mature individuals. —Schriften naturw. Ver. fur Schleswig-
Holstein, Bd. vi. Heft 1 (Atel, 1885).
On Adamsia palliata. By M. Favror.
The constant association of Adamsia palhata and Hupagurus
Prideauxi has long been known without having been made the
object of any special investigation. This association is equally for
the benefit of both animals—abundant and well-prepared food for
the Adamsia, the mouth of which is placed behind the foot-jaws
and. chelz of its associate, and a shelter adapted to the peculiar
structure of the Hupagurus, the ambulatory legs of which, extending
far at the sides and remarkably active, could not move easily with a
dwelling which was not so exactly fitted to the form of the animal.
Thus Hupaguri captured in the open sea and destitute of Adamsice
present, attached to the extremity of their abdomen, gasteropod
shells, which are always of very small dimensions, so as not to
interfere with the movements of the ambulatory feet. Hence when
these animals live separated from their habitual associate they are
imperfectly sheltered.
Another proof of the peculiar function of the Adamsia is that in
the association of two adult individuals the size of the Actinia is
always in relation to that of the crustacean, while the shell is most
frequently of very small dimensions. The latter therefore serves
chiefly as the common point of fixation of the two creatures.
Whatever may be the deformation presented by the adult Adamsia,
its anatomical structure is morphologically the same as that of other
Actiniz. It more particularly approaches that of Sagartia para-
sitica (Adamsia Rondeletii, Carus), the foot of which likewise
secretes a layer of mucus which acquires a membranous consistency.
The two species are furnished with six pairs of large primary septa
and six secondary, equally remarkable for their breadth; the
former are provided with sexual glands throughout their whole
extent, and advance much beyond the other folds towards the middle
of the gastric cavity. In both the acontia originate at the base of
the folds, immediately below the reproductive organs. Their origin
thus constitutes an excellent mark to indicate the base of the
column. This enables us to assert that in Adamsia the foot is all
156 Miscellaneous.
that part of the animal which secretes the parchment-like mucus,
although this part is not entirely attached, as in Sagartia parasitica.
The deformation undergone by the animal is due to the consider-
able expansion of this foot, carrying with it the lower part of the
column. This expansion becomes so great in the completely deve-
loped animal that the foot and the wall of the column become to a
great extent parallel. From this results the remarkable fact that
true gastric canals are formed by the elongation of the folds in a
horizontal direction.
The ovules before deposition are furnished with a germinal vesicle,
which we do not find after their escape. Fecundation is therefore
internal. Segmentation, which is very easily observed, takes place
regularly up to sixteen cells. The Morule are all of very irregular
form. They become transformed into Gastrule.
I have traced the further development to a larval form with
eight tentacles, the form in which fixation takes place. I have
also observed very small fixed Adamsie of hexameral type and not
yet deformed. Others, a little older, showed various degrees of
deformation. They show that the Actinia after attaining a certain
size upon the inner margin of the aperture of a gasteropod shell,
spreads out to the right and left, following exactly the outer margin
of the shell, but without concealing it at all. Wesee therefore that
the commencement of the deformation has as its result the sheltering
of the hermit-crab. It is only later on and secondarily that the
shell of the gasteropod is covered by the Adamsia—Comptes
Rendus, July 13, 1885, p. 173.
Note on “Deep-sea and Shallow-water Hydrozoa.”
By J. J. Quetcu, B.Se. (Lond.).
In the last Number of the ‘Annals and Magazine of Natural
History,’ in a paper ‘‘On some Deep-sea and Shallow-water
Hydrozoa,” a new species of Plumularia was described by me under
the name of Plumularia delicatula. It was quite overlooked by me
at the time that this name had already been applied by Mr. Bale to
an Australian Plumularia (Journ. Micr. Soc. Victoria, vol. .). For
the Cape-Verde species, which is thus destitute of a name, I substi-
tute the term “ annuligera,” suggested by the more or less ringed
extremities of the internodes ; so that the species should be known
as Plumularia annuligera.
ae ED NTS OF NUMBER 92.— Fifth Series.
2 “yu. cians on the Geocanhaeal Distribution of the Teas!
a “By Pig 0c SG GLE 0 GC Naa os aa 77
ie, we Second List of Reptiles and Batrachians from the Province
Rio Grande do Sul, Brazil, sent to the Natural-History Museum by
| a Dr. H. yon Thering. By G. A. BouLENGER ..... BAS Mion RRA RED gty 85
Xx. On the “Tag” of Coclopleurus Maillar he Mich. By Prof. P.
Maxrin SIGS) Ee RBG cs eae ore ty Maher tates, siren SRR WI Ay NB A 88
‘XI. Remarks on the Celenterate Nature of the Siiaees By
. Witnam AVERSA TAG yi uere lab amede Alay ach gilt v Rata eh ore aah eu tne ae: 90
XII. On some Points in the Morpholog y of the Echinoderms, and
more especially of the Crinoids. © By P. Hurperr Carpenter, D. Se.,
_ FE-R.S., Assistant Master at Eton College ..... Reg Samet SLR AR oA 100
XIII. Description of a new ‘Species of the Zetides Section of
Papilio. By F. Moors, ¥.28., ALS. 2. ee eee ee ee 120
_ XIV. A new Frog (Rana sternosignata) from Sind. By James A.
- Murray; Curator of the Kurrachee Municipal Museum .......... 1b.
Do's Description of two new Curculionide (Eetemnorhinus) from: 5%
. Marion Islands. By Cuarzes O. WatermousE.................. 121
XVI. On the Relationship of Ulodendron, Lindley sid Hutton, to
Eepidodendron, Sternberg; Bothrodendron, Lindley and Hutton ;
— Segrllaria, Brongniart ; and pe edt on, Boulay. By Rowert
ane MeGemug cr tates VE Gr VBI) eee Oot tito eve ie 123
BIBLIOGRAPHICAL N OTICEH.
re woe Pak of the Scientific and Learned Societies of Great Britain and
Ireland ; comprising Lists of the Papers read during 1884. before
Societies engaged in fourteen Departments of Research, with the
Names of the Authors. Compiled from Official Sources. Second
PAMPER e Cr eta the ee Lak aig emu T Ly Sa eas alae aay 139
| PROCEEDINGS OF LEARNED SOCIETIBS.
Manha Microscopical Club’. 22 doe Saye 140-149
Geological Society :—Notes on the Polyzoa and Foraminifera of the
Cambridge Greensand. By G. R. Vinz, Esq. .............. 149
MISCELLANEOUS.
On the Existence of a Nervous System in the Accelous Planarie and
of anew Sense-organ in Convoluta Schultz. By M. Yvus Detacr 150
| The Nest of the Fifteen-spined Stickleback. By Prof. Kart Mézrus 153
Freia ampulla, the Flask-Animaleule. By Prof. Karz Mosrus .... 154
On Adamsia palhata. By M. Pavnor’ sy. 0 kee aes 155
Note on “ Deep-sea and Poet oe Hydrozoa.” By J.J. Qurxcn,
PM OE A LONGS) - suis l vy sp uate a BAR Set ONG rua winlie painting 156
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XVII.—On Phenicurus.
By M. H. pe Lacaze-Dururers *.
WHILE investigating Tethys leporina in the spring, at the
Laboratoire Arago, I found in large quantities the curious
parasite which that mollusk bears attached to its sides.
Upon Phenicurus, which is the name of the parasite, we
have only very imperfect information; but it was known to
Rudolphi, Cuvier, and Delle Chiaje. This last naturalist,
who at first thought he was the discoverer of it and called it
Planaria, indicated how it is attached by its mouth to the
mamille which are observed in the middle of the inter-
branchial fossee of the Tethys; he recognized in the interior
of its body the numerous muscular bands which give it great
contractility, as also the chief part of its digestive tube; but
although he has given some good figures of the exterior of
the animal his indications of its organization, when given, are
very unsatisfactory.
A favourable opportunity having presented itself, the fol-
lowing are some of the facts which I have ascertained :—
The body of Phenicurus has the form of a boy’s kite; it
* Translated from the ‘Comptes Rendus de l’Académie des Sciences,
July 6, 1885, tome ci. pp. 80-35,
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 12
158 M. H. de Lacaze-Duthiers on Phoenicurus.
is flat, rounded at one of its extremities, and drawn out into
a point at the other ; sometimes this extremity is simple,
sometimes furcate, but whether single or double it is coloured
red, which justifies the name of Phenicurus.
The two surfaces are very different. One, the most ex-
tended, is marked with large black and whitish spots, washed
over with a general slight reddish tinge, which is very vari-
able in different individuals; it reminds one of the colouring
of the back of certain toads. The other, which is white, is
less extended, and margined by the former, which borders it
and forms a sort of raised pad all round it.
The rounded extremity of the body bears an oval pit,
pierced in the centre by an orifice. The skin of this pit is
fine, smooth, white, and nearly transparent; it is bounded by
a pad formed by the extremities of the two surfaces, which
differ in colour. .
This is all that we observe in the exterior of the animal.
When the Phenicurus is in a very lively state it is seen to
contract and change its form incessantly ; it twists and inflates
itself on the side of the marbled surtace, especially towards
the rounded extremity, which is then inclined towards the
whitish surface, and the body becomes bent. Thus one is led
to regard the surface covered with the pattern as the back of
the animal, and the white surface as the anterior or abdominal
art. .
5 Led away by this impression I first of all sought the
nervous system by opening the Phanicurus on the coloured
surface, but I found nothing, and it was only by resuming
the dissection from the opposite surface that I obtained any
results and displayed the centres of innervation.
The most normally constituted nervous system that I have
met with presents, as a centre, two ganglia, one left, the other
right, united by a long transverse commissure. From each
of these ganglia issue two principal nerves, a superior one
going to the neighbourhood of the mouth, an inferior one
descending towards the tail. These centres are distant from
one another and nearly lateral; they are situated at the junc-
tion of the anterior third of the body with the ‘inferior two
thirds, and thus the four superior and inferior nerves, with
the ganglia and the transverse commissure, form an H, of
which the branches are of unequal size. These ganglia are
small relatively to the size of the animal; they contain large
and not numerous nerve-cells with peculiar characters, which
will be referred to hereafter in the histological examination.
The numerous, transverse secondary nerves issue both from
the ganglia and from the large principal nerves to run into
M. H. de Lacaze-Duthiers on Phcenicurus. 159
all parts of the organism. ‘They are in general very slender,
very long, and most frequently much undulated, a condition
which is in relation to the movements of extension and con-
traction of the body. They are divided into two very constant
orders. Not far from the ganglia are given off some large
trunks, some of which run into the common tissue situated
within the muscular layers, which will be referred to further
on; while the others, traversing these layers, are distributed to
the subcutaneous tissue and probably arrive at the skin. This,
however, is difficult to make out by dissections or sections,
and the discovery of these terminations will be purely a matter
of chance.
Studied in a great number of individuals the nervous system
presents peculiarities which merit notice. The two superior
nerves are stout and terminate suddenly close to the buccal
orifice. I shall have to revert to this termination. Jn their
course they give off pretty numerous delicate branches which
run into the subcutaneous tissue of the buccal pit.
The nerves, as they depart from the centre, present from
point to point ganglionic inflations of very variable bulk and
composed of one, two, or three elongated cells, the larger axis
of which is parallel to their direction.
Another very remarkable peculiarity is the following :—I
think I have never met with two individuals presenting a
complete identity in the composition of the nervous centres.
The following are some of the arrangements observed :—
Sometimes there was only one median ganglion, from which
issued the two large buccal nerves and the two principal
nerves of the caudal extremity ; sometimes I have only met
with a sort of chain of three or four elongated ganglia placed
one after the other, a single nerve running towards the mouth
and another towards the tail. Lastly, in one case, I found
seven small ganglia arranged transversely and united not only
by a transverse commissure, but also by filaments forming a
network, a true plexus. In all cases, whatever may be the
number of the ganglia, the situation of the nervous system
as a whole, with regard to the digestive tube and the muscles,
continues the same, and the filaments are distributed in part
to the middle of the body and in part to the subcutaneous
layers.
Finally, it is not uncommon to find only a single buccal
nerve, and in this case the nerve is stouter; and I have seen
the two buccal nerves issue from the same ganglion.
To sum up, the position of the nervous system is constant,
but its forms vary infinitely.
I have still to note this fact—I found a transverse cord
12*
160 M. H. de Lacaze-Duthiers on Phoenicurus.
issuing from the buccal nerves and uniting them, passing in
front of the digestive tube. Was this an cesophageal collar
or a simple anastomosis ?
Pheenicurus presents a very interesting histological consti-
tution, which will form the subject of a separate memoir. I
shall say but little about it at present. Its body has no general
cavity, it is therefore acwlomatous ; but it is filled up with a
cellular-fibrillar tissue showing nuclei, in the midst of which
and soldered to it are various organs and large cells or vesicles
which are often visible to the naked eye, and may acquire
enormous dimensions.
Under the skin, after a layer of connective tissue, we find
long muscular bands regularly spaced and forming two
lamine, one dorsal, the other abdominal, passing to the buccal
and caudal extremities. Between these two laminz is the
central part. The body is in this way divided into three
zones, two external to the muscular bands and one interme-
diate. Further other fibres, also muscular, but transverse and
exterior to the former, to which they are attached, crossing
them at right angles, form a true trellis, which is easily dis-
covered ; for it appears very evidently so soon as one opens
the body of the animal and removes the integuments. At the
sides, to the right and left, there are also bundles of muscuiar
fibres passing perpendicularly from one surface to the other,
which assist in limiting the central space.
It is in this median intermuscular space that we find the
digestive tube, the central nervous system, and a special gland,
the only organs that I have been able to observe.
The digestive tube commences at the central orifice of the
pit noticed towards the rounded extremity, and descends to
the tail. Sometimes, after leaving the mouth, it presents a
dilatation followed by a constriction, indicated by Delle Chiaje;
but great importance must not be attached to this arrange-
ment, which varies with the state of the individuals.
The tube, which is sometimes even, sometimes irregular,
narrowed, or dilated, descends narrowing to the neighbourhood
of the tail, and throughout its length, as in all directions, in
front, behind, and on the sides, gives origin to branches,
which ramify infinitely, traversing the muscular interstices,
and extending by their delicate branches into the vicinity
of the integuments. From this point of view Phenicurus
is a very characteristic Dendrocelan.
The walls of the digestive tube, which are of extreme deli-
cacy, easily escape observation if they are not filled with some
coloured material or submitted to the action of some reagent
which reveals their presence. I have not found any anus,
M. H. de Lacaze-Duthiers on Phoenicurus. 161
The last organ of which I was able to ascertain the exist-
ence is a very simple gland formed by a tube terminating in
one or two ceca, and bearing some rare lateral ceca. One
of them, directed towards the white surface of the body, but
not extending to the integuments, is constant and larger.
This gland is situated towards the marbled surface, and opens
into the buccal orifice itself. What are its functions? It is
difficult to say, although it seems natural to regard it as a
salivary gland.
I have proved that what Delle Chiaje regarded in Tethys
as an aquiferous apparatus was nothing but the venous appa-
ratus of the mollusk, opening externally at the apex of the
papilla situated in the centre of the interbranchial fosse.
The Phenicurus, grasping this papilla with its mouth, can
therefore at any moment suck in the sanguine fluid of the
Tethys, of which it is the parasite in the most exact accepta-
tion of the word.
From what has been stated it is now easy to place and
orientate the animal. Placing the nervous system posteriorly,
the white surface evidently represents the back, and the
marbled surface is anterior; the mouth being placed above,
all the positions are easy to characterize and indicate. Hence
to find the nervous system we must open the Phwnicurus at the
back, and remove the subcutaneous tissues, and it is in front
of the muscular bands that we discover the ganglia ; then it
will be seen that in passing from back to front we find the
nervous system, the digestive tube, and the salivary gland.
Phenicurus appears to me to be very distinctly characterized
as a Dendrocwlan by the absence of the abdominal ganglionic
chain and by the arrangement of its arborescent intestine.
To fix more completely its zoological relations it would be
of service to have traced its evolution. Now, in the month of
May, I was unable to discover the organs of reproduction ;
only once I found an individual in which the large cells above
mentioned had acquired enormous proportions. The skin of
the animal being torn, they projected outwards like bunches
of grapes. I will not assert that they represented ova, for all
questions relating to reproduction remain to be cleared up.
It is important that 1 should repeat that my observations were
made in the month of May, and that, in the animals preserved,
I have not met with reproductive organs, which are so easily
recognized in the Turbellaria or the '[rematoda.
Does Phanicurus represent only a period or a stage of its
whole existence? Is it a creature deformed or degraded by
parasitism ? Is its evolution accomplished under varied forms
162 Mr. R. Kidston on the Relationship
in different stations? These questions are equally curious
and interesting to solve.
I have had the Phenicurus in abundance at the Laboratoire
Arago. My boat, every time it went out to seek specimens
of Zethys tor me, brought me a great number of all sizes,
free or fixed. I hope, therefore, shortly to elucidate this still
obscure history.
XVIII.—On the Relationship of Ulodendron, Lindley and
Hutton, to Lepidodendron, Sternberg; Bothrodendron, Lindley
and Hutton; Sigillaria, Brongniart ; and Rhytidodendron,
Boulay. By Rosert Krpston, F.G.S8.
[Plates HI—VII.]
[Continued from page 139. ]
II. DESCRIPTIONS OF SPECIMENS.
Lepidodendron Veltheimianum, Sternberg.
Specimen No.1. From Burghlee Pit, Loanhead, Midlothian
(Carboniferous Limestone Series). Pl. III. fig. 1 (nat. size).
—This fossil, which is represented by an ¢mpression of the
plant in a fine-grained micaceous sandstone, is 15 inches long
and at its broadest part about 44 inches wide, Towards its
upper part it shows one of the characteristic Ulodendroid
sears, which is 44 inches high and 24 inches wide. The
central umbilicus is situated about 2 inches above the lower
margin of the scar. On the lower surface of the Ulodendroid
sear, and extending slightly above and around its umbilicus,
are rows of little “dots”? arranged in spirals, converging
towards the umbilicus. ‘The little “ dots ” indicate the posi-
tion of the vascular bundles of the aborted leaves, and become
closer to each other as they approach the umbilicus. On the
upper part of the scar is a number of straight lmes which
radiate from the umbilicus ; these are the impressions of the
basal leaves or bracts of the appendicular organ. The um-
bilicus is slightly raised. On other parts of the specimen
are seen the impressions of the leaf-scars, which are, in form
and arrangement, similar to those of Lepidodendron Velt-
heimianum. 'To the left of the fossil the leaf-scars are
obliterated by a longitudinal splitting of the bark.
As the specimen is only an impression it must be remem-
bered that the elevations on the fossil were depressions in the
plant.
of Ulodendron to Lepidodendron, &e. 163
Specimen No. 2. From Straiton Oil Shales, near Edin-
burgh (Calciferous Sandstone Series).—This example is
a fragment of what must have been a large stem. The
specimen, which is an impression in very fine-grained
bituminous oil shale, measures 9 inches in length by nearly
8 inches in breadth. ‘Towards the centre are shown two
Ulodendroid scars, about 15%; inches long, by 1,% inches
broad, standing rather less than 14 inches apart. This
example is chiefly interesting from the absence of the
longitudinal fissures which are so characteristic of these
Ulodendroid stems. As a consequence, from the increase in
girth of the stem, the leaf-scars are much broader than in
those examples where the bark is longitudinally fissured.
This specimen shows a similar change in the lateral extension
of the leaf-scars to that w ich occurs in the older stems of
Lepidodendra which do not bear Ulodendroid scars. The
leaf-scars on this fossil are very similar in general form to
the figure of Sagenaria Veltheimiana given by Romer in
‘ Paleontographica,’ vol. ix. pl. ii. fig. 6, only in the
British specimen their breadth is greater in proportion to
their length ; they are, in tact, nearly as broad as long.
Specimen No. 3. From the Oil Shales, West Calder, Mid-
lothian (Calciferous Sandstone Series).— Specimen in the
coliection of the Addiewell Oil Co., Addiewell. Pl. IV.
fig. 2.—This figure shows a portion of a large stem of Lepr-
dodendron Veltheimianum, 25 inches long and about 4 inches
wide. ‘The greater part of the fossil shows the outer surface
of the stem, on which are exhibited, in a very early state ot °
development, three Ulodendroid scars and a part of a fourth.
The Ulodendroid scars, from centre to centre, are 54 inches
apart. ‘They are slightly elevated, and do not show a clearly
defined umbilical nodule, having an appearance as if the
appendicular organ had been forcibly removed. In this early
condition of development of the Ulodendroid scar, the appen-
dicular organ appears to have been attached at its upper
margin. Another interesting point shown by this example
is the presence of the ordinary leaf-scars on the Ulodendroid
sear. ‘These are a continuation of the ordinary series of the
leaf-scars on the stem, and converge from all sides to the
centre of the upper margin of the slight inflation. As there
is here the outer surface of the stem, it is clearly shown that
in the elementary condition the part bearing the appendicular
organ stood at a slightly higher level than the rest of the
bark. This inflation, however, eventually became effaced by
the increase of the stem causing the bark to swell up around
the base of the appendicular organ, and by this means the
164 Mr. R. Kidston on the Relationship
originally slightly elevated cushion is converted into a circular
or oval depression. The point of attachment of the appen-
dicular organ in this example is in the centre of the upper
margin. ‘This point represents the umbilicus of the older
scars. The part of the depression above the umbilicus on
older stems is therefore entirely caused by the pressure of the
base of the appendicular organ upon the bark.
The leaf-scars are elongated -rhomboidal, and slightly
raised above the surface. ‘Those of each series are connected
with each other by a flexuous ridge. The vascular bundle
dots are not shown, but the position of the vascular scar is
indicated by a little ridge.
The bark at this age shows no traces of the longitudinal
clefts which are so characteristic of older examples.
The full width of the stem at its lower portion is about 4
inches, and that this is its complete breadth is proved by the
impression of one of the Ulodendroid scars of the correspond-
ing opposite vertical row occurring in the matrix where part
of the stem has been removed. ‘The surface of the bark
between the leaf-scars, at certain parts of the stem, is orna-
mented with fine ridges, though they are not present, or
only feebly so, on the small portion which forms the subject
of figure 2. .
Specimen No. 4. From Dalmeny, Linlithgowshire (Calci-
ferous Sandstone Series). Collected by Dr. Macfarlane.
Pl. IV. fig. 3 (nat. size) This specimen, which measures
about 6 by 44 inches, is preserved in a very fine-grained
bituminous oil shale. The leaf-scars are fusiform and slightly
elevated, those of the same series being connected with each
other by a slightly raised flexuous ridge. ‘The surface of the
bark between the leaf-scars is beautifully ornamented with
fine, somewhat irregularly placed wavy lines. The vascular
scar is not clearly shown, but appears as a slightly raised
point towards the upper part of the leaf-scar. As the example
only shows one of the outer margins of the stem, its original
width cannot be ascertained. ;
Specimen No. 5. From West Calder, Midlothian (Caleci-
ferous Sandstone Series). Pl. LV. fig. 4 (nat. size).—This
figure shows a small portion of an impression of a large stem,
which is fully 2 feet long. The upper portion apparently
represents the complete breadth of the stem, which is 7 inches
across. The specimen shows no sign of any Ulodendroid
scar. The leaf-scars are elongated-rhomboidal or fusiform,
those in one series connected with each other by a ridge.
The vascular scar is situated towards the upper part of the
of Ulodendron to Lepidodendron, cc. 165
leaf-scar, but its details of structure are not shown. The
leaf-scars are almost contiguous, being only separated laterally
from each other by the caudate extension, which runs from
the apex of one scar to the base of another. The bark is
much cleft by longitudinal fissures ; a portion of one of these
is shown in the figure. The matrix on which the impression
has been stamped is a very fine bituminous oil shale.
This example also shows at certain parts the same charac-
ter, though not so strongly carried out, as in the specimen of
Lepidodendron acuminatum mentioned by Stur, Culm-Flora,
p- 398, pl. xxii. (xxxix.) fig. 4, where the leaf-scars some-
times seem to lose their spiral arrangement, and appear to
be placed in vertical rows, simulating somewhat in this pecu-
liarity a sigillartan arrangement of leaf-scars.
Specimen No. 6. From Blackbraes, West Calder, Mid-
lothian (Calciferous Sandstone Series). Collected by J. Linn,
Esq. Pl. VI. fig. 11.—The specimen, shown in fig. 11
reduced to 4 natural size, measures in its greatest length 7
inches, its width being about 4 inches. The fossil shows part
of a stem, which must have been of considerable size. ‘The
small fragment of it that has been collected, still retains its
rounded form, and seems to have suffered little from pressure.
The matrix of this example is a fine-grained sandstone, and
though the leaf-scars are not very well shown, at a, fig. 11,
they are sufficiently well preserved to admit of a satisfactory
specific determination. The Ulodendroid scar is almost cir-
cular, considerably depressed, and measures about 14 inches
in diameter. ‘I'he basal portion of the appendicular organ
which fits into the scar has also fortunately been preserved.
This is shown in profile at fig. 11 4, and a view of its basal
aspect is seen at fig. 11c¢; both of these figures are natural
size. ‘The outer surface of the fossil is discoloured by the
carbonaceous matter of the plant. This is especially marked
on the surface of the depressed Ulodendroid scar, and on the
base of the appendicular organ, which, with the exception of
a very small spot towards the centre of each, indicating
the point of attachment of the appendicular organ, are
stamed dark brown. Had the appendicular organ been
attached to the stem by the whole of its surface, its base and
the surface of the Ulodendroid scar could not have been
covered with carbonaceous matter. ‘To the right of fig. lle
are see in the matrix what may possibly be the remains of
leaves. In the profile, fig. 11 6, the markings on the outer
surface of the appendicular organ have very much the appear-
ance of leat-scars, but cones, when the upward extending
portion of their bracts is broken off, have also a resem-
166 Mr. R. Kidston on the Relationship
blance to ordinary leaf-scars, as is well shown in Sir Joseph
Hooker’s plates of Lepidostrobi*. This specimen, therefore,
does not, unfortunately, help us to decide whether stalked or
sessile cones were attached to the Ulodendroid scars.
At fig. 11 @ is shown, natural size, the small portion of the
stem marked a, fig. 11. This part is at a slightly lower level
than the rest of the outer surface of the fossil, and the leaf-
scars are slightly larger; it is therefore probable that this
fragment of the specimen is not in its true position.
This example shows no traces of longitudinal clefts in the
bark.
Specimen No. 7. From Addiewell, Midlothian (Calciferous
Sandstone Series). Collected by Dr. Macfarlane. — This
example, which is about 4 inches high and 43 inches wide,
shows towards the left side of the fossil a Ulodendroid scar.
This is oval, and measures across the umbilicus about 7/5 of
an inch. Its upper border is clearly defined, but the lower
portion of the scar, from the umbilicus downward, gradually
assumes the appearance of the ordinary leaf-scar- covered bark,
being clearly covered with broadly-fusiform leaf-scars, similar
in shape to those occurring on other parts of the stem and
belonging to the same spiral series. The leaf-scars on the upper
part of the Ulodendroid scar are, however, obliterated.
Specimen No. 8. From 'lodholes, on the Bannoch-Burn,
about 5 miles S.W. of Stirling (Carboniferous Limestone
Series).—This specimen is the impression of a portion of an
old and much-cleft stem. The fossil measures about 11
inches in length and 8 in breadth. The main interest of
this example lies in the numerous ridges (the casts of the
clefts in the bark) which occur on its surface. Hvidently
these ridges originally stood up at right angles to the
surface of the impression, but have been flattened or bent over
by subsequent pressure, and now hide the leaf-scars beneath
their extended surface. Some of these ridges have at different
parts of the fossil been broken off, and show that their line of
attachment to the fossil is comparatively small in proportion
to the superficial area they now in their flattened condition
present. As an instance, the width of one of these ridges
measures fully 38, of an inch, but where it is broken off, the
line which represents the original width of the cleft, and on
which no leat-scars are seen, only measures 7g of an inch;
the remaining 34; inch of the flattened ridge is simply superin-
* Memoirs of the Geol. Survey of Great Britain, vol. 11. pt. il. p. 440,
pls. iv., vii., & viii, 1848. (Remarks on the Structure and Affinities of
some Lepidostrobi. )
*
of Ulodendron to Lepidodendron, &c. 167
cumbent on the surface of the stem, and hides beneath it
the impressions of the ordinary leaf-scars.
As these ridges are often more a bending over to one side
than a flattening out of the ridge, probably the surface they now
present represents the original depth of the clefts in the bark ;
if this view is correct, in this case they cannot have been much
less than aninch deep. ‘The form of the leaf-scars is broadly
fusiform, and they agree well in character with those of
Sagenaria (Lepidodendron) acuminata, Géppert *.
Specimen No. 9. From same locality as No. 8.—On another
Impression, which is about 6 inches high and 10 inches
broad, the flattening of the casts of the clefts in the bark is
carried to a greater extent than in the last specimen. Overa
space of about 54 inches, the whole of the leaf-scars are
obliterated by the flattening of what appear to have been 7
ridges (the casts of what were originally 7 clefts in the bark).
This is succeeded by a vertical band of about 1 inch wide, on
which the impressions of the leaves are shown; succeeding
this there is another ridge about 7) of an inch wide, then
another vertical band exhibiting the leaf-scars 14 inch wide,
then another flattened ridge fully an inch wide. Impressions
ot Lepidodendron Veltheimianum, on which the leaf-scars are
quite obliterated by these flattened ridges, have been handed
to me several times as Sigillarian stems.
Specimen No. 10. Lepidodendron (Veltheimianum ?). From
Grange Colliery, Bo’ness, Linlithgowshire (Carboniferous
Limestone Series). Collected by H. M. Cadell, Esq.—This
specimen occurred along with numerous examples of Lepido-
dendron Veltheimianum ; but as none of the leaf-scars are seen
on the fossil, it would be unsafe positively to refer it to that
species. It represents the impression of a fragment of a very old
stem, from which all traces of the leaf-scars have been oblite-
rated by longitudinal furrows; these have rounded surfaces,
and do not run continuously for any great length, but as soon
as one ceases, another originates to take its place. It appears
to have been a similar condition of an old Lepidodendroid
stem that has given rise to the Lyginodendron Landsburgit,
Gourlie f. A somewhat similar state of an old stem of Lepido-
dendron has been figured by Sir William Dawson{. Probably
the Bo’ness example only represents a further stage of the
* Foss. Flora d. Uebergangsgebirges, pl. xxiii. fig. 4, and pl. xliii. fic. 8.
+ Proceed. of Phil. Soc. of Glasgow, vol. i. pt. 1. p. 108 (1841-44), I
am doubtful if the plant whose curious structure has been so fully ex-
plained by Dr. Williamson as Lyginodendron Oldhamw has any con-
nexion with the genus Lyginodendron of Gourlie.
t+ Acadian Geol. 2nd ed. p. 445, fig. 170 ¢ (1868).
168 Mr. R. Kidston on the Relationship
longitudinal fissuring of the bark mentioned as occurring in
the last described specimen of Lepidodendron Veliheimianum.
Specimen No. 11. Small branches and stems of Lepedoden-
dron Veltheimianum, in a beautiful state of preservation, with
the leaf-scars similar to that figured by Géppert in his Foss.
Flora d. Uebergangsgebirges, pl. xxiii. figs. 1-3, are extremely
abundant at many localities in the Calciferous Sandstone
Series in the neighbourhood of Edinburgh. There also occur
frequently examples with leat-scars which agree in character
with those named Lepidodendron (Sagenaria) elliptica by
Goppert * (PIL. IV. fig. 4). This is a common form of Lepz-
dodendron Veltheimianum in Scotland.
Sigillaria discophora, Konig, sp.
Specimen No. 12. From Devonside, Tillicoultry, Clack-
mannanshire (Coal Measures). Collected by Mr. ‘T. Mitchell.
Pl. VII. fig. 12 (nat. size).
This example is preserved in a fine-grained micaceous
sandstone, and is the impression of the plant. The outer
layer of the bark is converted into a bright coaly matter,
which has adhered to the matrix ; hence the fossil shows the
inner surface of the outer cortical layer. ‘Towards the lett is
seen a portion of a Ulodendroid scar, on whose surface are
exhibited in series, which evidently converge towards the
umbilicus, several rows of elevated little dots that mark the
position of the vascular bundles of the aborted leaves. The
remainder of the fossil is covered by the leaf-scars, which
vary much in size and shape. Ata, fig. 12, they are very
small, some only measuring about ¢ of an inch in their trans-
verse diameter; their upper and lower angles are rounded,
the lateral angles sharp and prominent. The vascular-bundle
sear is slightly above the centre.
On the greater portion of the specimen the leaf-scars are
rhomboidal, the boundary-line of the leaf-scar being slightly
raised. The position of the vascular bundle is usually indi-
eated by a small tubercle, but sometimes this appears to be
double. On none of the leaf-scars are the vascular-bundle
impressions clearly seen.
Remains of the foliage are indicated at several points at
the margin of the specimen. ‘The leaves appear to have been
very narrow and long, and are single-nerved. ‘Their complete
length is not shown, all of the leaves being imperfectly pre-
served. Figs. 12a@ and 126 show a few of the leat-scars
enlarged, to illustrate their variation in form on the same
* Goppert, Zc. pl. xiii. fig. 7.
of Ulodendron to Lepidodendron, &c. 169
example. ‘These two figures correspond to the parts lettered
a and 6 on fig. 12. ;
Specimen No. 13. Locality: “Coal Measures, British.”
Specimen in the collection of the Geological Survey of Great
Britain, Museum of Practical Geology, Jermyn Street, Lon-
don. Pl. V. fig. 8 (nat. size)—This is one of the most
beautiful specimens of Sigillaria discophora, Konig, sp., that
I have seen. It is about 34 inches square. Towards the
right there are two Ulodendroid scars, from the umbilicus of
which very slightly elevated ridges radiate on all sides. A
small part of the outer cortical layer has been removed, but
on the portion which shows the outer surface of the stem the
leaf-scars are well preserved. Their transverse diameter is
slightly greater than their vertical height; the upper and
lower angles are rounded, and the lateral angles prominent.
The scar of the vascular bundle is situated towards the upper
part of the leaf-scar, and slightly above the centre.
Where the outer layer of the bark has been removed, the
inner surface exhibits delicate markings, among which are
conspicuous the little elevated “ dots” that mark the position
of the passages for the foliar vascular bundles. ‘This latter
condition of the stem forms the genus Bothrodendron, Lindley
and Hutton. The two Ulodendroid scars have evidently
almost touched each other; but this character is slightly
obscured, on account of the lower edge of the upper Uloden-
droid sear having been slightly broken.
My thanks are due to Dr. A. Geikie, Director-General of
the Geological Survey of Great Britain, for kindly allowing
me to figure and describe this interesting example.
Specimen No. 14. From Furnace Bank Pit, Old Sauchie,
Clackmannanshire (Coal Measures). Pl. VII. fig. 13 (2 nat.
size).—The specimen, the figure of which is a quarter natural
size, measures fully 16 inches long by 11 inches broad. It
is preserved in a fine-grained, purple micaceous sandstone.
The fossil is an impression of what must have been a very
large stem; adhering to its surface is part of the epidermal
layer of the bark. Towards the right of the fossil are por-
tions of two large Ulodendroid scars, whose vertical height is
about 34 inches. Owing, in part, to the age of the specimen,
and in part to its state of preservation, the leaf-scars assume,
at some portions of the stem, an almost quadrangular form,
and show at their centre a large rounded tubercle. Some
such leaf-scars are shown, natural size, at fig. 13a. On other
parts of this specimen the Bothrodendron condition is exhi-
bited. A small portion of the stem, showing this state, is
represented, natural size, at fig. 13 6. Here there are ar-
170 Mr. R. Kidston on the Relationship
ranged, in quincuncial order, rows of shallow elongated pits,
the channels through which the foliar bundles passed to the
leaves. The impression bears numerous longitudinal ridges,
which are more or less interrupted: during their course; they
cease after extending some distance, when others spring up
alongside of those which have terminated, and continue their
course in the same direction. On the reduced sketch, fig. 13,
the leat-scars are rather too small.
Specimen No. 15. From the same locality as No. 14. PL.
IV. fig. 5 (nat. size).—This specimen is the impression of
a small fragment of the outer surface of the bark, showing
the rhomboidal leaf-scars. The upper and lower angle of the
leaf-scar is rounded; the lateral angles are prominent. In
the compressed state in which the fossil occurs the leaf-scars
appear as if separated by an interval, but this interval is the
impression of the slightly raised cushion on which the leaf-
scar is situated. At the part marked a, fig. 5, the intervening
space between the leaf-scars shows a central line, clearly
indicating that it belongs in part to the two contiguous leaf-
sears, and is, in fact, the now compressed cushion whose area
slightly exceeded that of the leaf-scar which it bore. Fig. 5a
shows a few of the leaf-scars enlarged. ‘The vascular-bundle
scar is situated towards the upper part of the leaf-scar, and is
only indicated in this example by a single “dot.” Towards
the centre and right hand of the specimen the bark is seen to
be longitudinally split *.
Sigillaria Taylort, Carruthers, sp.
Specimen No. 16. From Camps Lime Quarry, Midcalder, Mid-
lothian (Calciferous Sandstone Series). Collected by the late
R. F. B. Hislop, Esq., Edinburgh. Pl. IV. fig. 6 (nat. size).
The greater portion of this specimen is badly preserved,
and nothing further is shown on the fossil than that repre-
sented in fig. 6. Of the two Ulodendroid scars, the upper is
much larger than the lower. On the upper part of both is
seen a row of slightly elevated ridges arranged in a semi-
circle. These are evidently casts of the channels through
which the vascular bundles passed to the aborted leaves.
The chief point of interest afforded by this example, which
exhibits the true outer surface of the bark, is the beautifully
preserved leaf-scars seen to the right of the lower Uloden-
droid scar. A few of these are enlarged in fig. 6a.
The leaf-scars are rhomboidal, slightly elevated, very small,
being little more than one tenth of an inch in transverse dia-
meter; their upper and lower angles are rounded, and their
* Figs. 5 and 5a are drawn on the Plate in inverted position.
of Ulodendron to Lepidodendyon, cc. 171
lateral angles sharp. The cushion on which they are placed
very slightly exceeds the size of the leaf-scar. ‘The vascular-
bundle impression is situated a little above the centre of the
leaf-scar.
Specimen No. 17. From the Oil Shales, Addiewell, Mid-
lothian. In the collection of the Addiewell Oil Company
(Calciferous Sandstone Series). Pl. VL. fig. 10, 10 6, c,d
(fig. 10, 4 nat. size; fig. 10, c, d, nat. size).
This specimen, which is preserved in a fine-grained bitu-
minous oil-shale, exhibits the termination of a branch. It
measures 152 inches in length and 4 inches in breadth.
Very little of the fossil proper is preserved, the greater part
of the example showing only the impression of the plant.
The part marked a, fig. 10, 1s a small portion of the outer
surface of the plant. That lettered b, c, d shows the inner
surface of the outer cortical layer, and that marked e, e the
impression of the outer surface of the stem in the matrix.
We must now enter more fully into the description of the
various parts of this instructive specimen. On the small part
of the fossil proper which is preserved (fig. 10 a) there is only
a portion of one of the Uledendroid scars shown; this occurs
as a circular depression about 2 inch wide. The opposite
and corresponding row of Ulodendroid scars occurs on that
part of the specimen lettered in the figure 0, c,d. The epi-
dermal layer of the bark has here adhered to the matrix, a
circumstance which frequently takes place in this group of
fossils, so that the view presented of this part is the cnner
surface of the outer cortical layer. On this are seen the casts
of twelve Ulodendroid scars; and as they are looked at from
the inside of the stem, they appear as elevations. In form
and size they vary considerably. Many of them touch each
other, but some are separated by a slight interval. A few
are almost circular, whilst others are more or less elliptical ;
and occasionally, when two Ulodendroid scars come in con-
tact, their sides become somewhat flattened from mutual
pressure. The largest of these scars measures transversely
1;5 inch, the smallest about 745 inch. The scar lettered ec,
fig. 10, is shown natural size at fig. 10c. The whole of
its surface is covered with little dots arranged in spirals, some
belonging to series which do not converge towards the
umbilicus, but go past it.
None of the Ulodendroid scars, of course, on the part let-
tered b, c, d show the straight or slightly bent bands on their
upper part, which so commonly radiate from the umbilicus of
Ulodendroid scars, as we are viewing the ¢nner surface of the
outer cortical layer; this also explains why the little “ dots”
172 Mr. R. Kidston on the Relationship
of the foliar bundles are exhibited so distinctly on their upper
portions.
At 6, fig. 10, the form of the leaf-scars is shown; these
are represented natural size at fig. 106. ‘This view likewise
shows the znner surface of the outer cortical layer, and only
gives a general idea of their form, which is rhomboidal.
Slightly above the centre the channel through which the foliar
vascular bundle has passed is indicated by a little “ dot.”
At d, fig. 10, is exhibited the Bothrodendron condition of the
fossil; this is represented natural size at fig. 10d. Here
all trace of the leaf-scar is obliterated, and nothing is left to
indicate its position except the little “ dots ” which mark the
channels of the foliar vascular bundles.
At e, fig. 10, is seen the impression of the outer surface of
the stem. The form of the leaf-scars is not shown, as the
specimen has been thickly covered with foliage; many of the
leaves are seen extending past the margins and apex of the
fossil. :
This specimen is very interesting as exhibiting the termi-
nation of a branch, and is, so far as I know, the only speci-
men extant which shows that character.
Hugh Miller refers to a similar example, but, unfortunately,
it has been lost*. The branch appears to have suddenly
terminated in a truncated or obtuse apex, to the very summit
of which were borne the Ulodendroid scars.
Specimen No. 18. From the bituminous Oil Shales (Cal-
ciferous Sandstone Series). Collected by Dr. Macfarlane.
Pl. V. fig. 9 (nat. size).
The specimen, of which the sketch is natural size, is about
A inches high by about the same wide. On the left of the
plant are seen attached four of the upward directed appen-
dicular organs. ‘These, as well as the stem, are covered by
foliage, but most of the leaves on the stem are broken off, and
only their bases now remain attached to the leaf-scars.
The leaves or bracts on the appendicular organs are closely
adpressed, and are best seen on that second from the base.
The appendicular organs are in so young a state of develop-
ment, that from any points they show it would be unsafe to
state definitely whether they are sessile or stalked cones ; but
I incline to the former view. A portion of the fossil towards
the lower part of the specimen has been removed, and on the
matrix is seen the impression of one of the Ulodendroid scars
of the opposite and corresponding row. From this we gather
that the full width of the specimen could not have been much
greater in its compressed state than 4 inches. The appendi-
* ‘Testimony of the Rocks,’ ed. 1857, pp. 462-464.
of Ulodendron to Lepidodendron, ce. 173
cular organs, which stand out in some relief, are about 2 inch
long and nearly as broad, and appear to have had rounded
apices. The fourth and uppermost appendicular organ is not
well shown, being partly covered with the matrix. From
the presence of the foliage, the form of the leaf-scars cannot
be seen.
Specimen No. 19. From the bituminous Oil Shales, Straiton,
near Loanhead, Midlothian (Calciferous Sandstone Series).
This specimen is a portion of a branch about 1 foot long
-and 3 inches wide. Itshows a vertical row of twelve Uloden-
droid scars, and is mainly interesting as partly exhibiting the
true outer surface of the stem, in which occur a few longi-
tudinal clefts.
III. GENERAL CONCLUSIONS.
The point in which lies the essential generic difference
between Lepidodendron, Lepidophloios, Sigillaria, and Rhyti-
dodendron is the form and structure of the leaf-scar. My
apology for referrmg to the generic characters of three such
well-known genera as Lepidodendron, Lepidophloios, and
Sigillaria is that their generic differences form the basis of
my subsequent remarks. I am aware that, in addition to the
structure of the leaf-scar, there are other points of minor
importance which enter into the definitions of these genera ;
but as far as the subject which specially occupies our atten-
tion at present is concerned, we shall not require to enter
more fully into the generic differences of the above-mentioned
four genera other than those characters derived from the struc-
ture of the leaf-scar, the mode of the attachment of the leaf
to the scar, and the cortical extension on which, in some cases,
the leaf-scar is supported.
These four genera may be briefly defined as follows :—
-LEPIDODENDRON. CEE AVE ies 3)
Leaf-scars contiguous or distant, rhomboidal or fusiform,
consisting of a ‘‘field” (c) and vascular-bundle scar (a), which
is usually situated towards the upper part of the field. The
vascular-bundle scar is transversely rhomboidal, its upper and
lower angles rounded, the lateral angles more or less promi-
nent. WVascular-bundle cicatricules three, punctiform (6). Im-
mediately beneath the vascular-bundle scar are two small
oval pits (d), one placed on each side of the median line (/).
Above the vascular scar and on the medial line is the “ ligule ”’
depression (¢). Leaf-base attached to the whole area of the
leaf-scar (including the “ field”).
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 13
174 Mr. R. Kidston on the Relationship
LepipopHoios. (PI. VII. fig. 14.)
Leaf-scars unprovided with a field and reduced to the vas-
cular scar (a), which is placed at the lower extremity of a
downward-directed cortical cushion (g) ; its upper and lower
angles are rounded, the lateral angles prominent. Vascular-
bundle cicatricules three, punctiform, the central one sometimes
triangular. On the cushion, above the leaf-scar, there occurs
in some species a small tubercle. Leaf attached to the vascular
scar only. Cushions to which the leaves are attached im-
bricated.
SIGILLARIA. (PI. IV. fig. 7.)
Leaf-scars unprovided with a “ field,” and reduced to the
vascular scar. Stems smooth or furrowed.
(A) Stem smooth.—Leaf-scars distant (Liodermarie) or
contiguous (Clathrarie, fig. 7), and placed in more or less
elevated cushions.
(B) Stems furrowed.—Leaf-scars in vertical series, distant
or contiguous (Rhytidolepis).
(In A & B.) Vascular scar more or less rhomboidal; upper
and lower angles rounded; lateral angles prominent. Vas-
cular-bundle cicatricules three, central punctiform or more or
less transversely elongated ; the two lateral lunate or linear.
Leaf-attachment restricted to the area of the vascular scar.
RHYTIDODENDRON, Boulay.
(Bothrodendron, Zeiller, not Lindley and Hutton.)
Leaf-scars wnprovided with a“ field,” distant, and reduced
to a vascular sear, which is transversely oval or quadrate,
with rounded angles, very small, in the two described species *
not 7 inch in diameter. Vascular-bundle cicatricules three,
punctiform.
As the form of the leaf varies among the species of a given
genus, being in Lepidodendron and Sigillaria either long and
egrass-like or short and lanceolate, its shape only becomes a
specific character.
The fructification of these plants is still imperfectly
* Rhytidodendron minutifolium, Boulay, and R. punctatum, Zeiller, sp.
The former species I have seen from two localities in the Scotch Coal
Measures—from débris at Keliybank Pit, Dollar, Clackmannanshire,
and also from Bonnington Pit, Kilmarnock, Ayrshire (in the collection
of Rey. D. Landsborough, Kilmarnock).
The plant I place here as R. punctatum, Zeiller, sp., was described by
that botanist as Bothrodendron punctatum, L. & H. See Ann. d. Science.
Nat. 6° sér., Bot. tome xiii. p. 218, pl. ix. figs. 1-3; also Végét. foss. du
terr. houil. p. 116.
of Ulodendron to Lepidodendron, cc. 175
known. In Lepidodendron and Sigillaria* it consisted of
cones, and in Rhytidodendron it was probably of a similar
nature. In certain Sigillarie and Rhytidodendra (R. punc-
tatum) there is also occasionally a small tubercle above the
leaf-scar or on some other part of the back (Stg. spinulosa,
Germar)f.
The evidence afforded by the various specimens which have
been described in the earlier part of this communication, as
well as that derivable from examples figured and described
by previous writers on this subject, may now be summarized,
when I hope to show that plants not only belonging to Lepi-
dodendron, but also to Stgillaria and Rhytidodendron, possess
large scars, arranged on their stems in two opposite vertical
rows.
Lepidodendron Veltheimianum, Sternberg.
It has been stated by some authors (Brongniart, Schimper,
and others) that the leaf-scars on the stems of Ulodendron
were always smaller than those occurring on the stems of
Lepidodendron of a similar size, and also that the vertical
clefts which occur in the bark of Ulodendron were not com-
mon to Lepidodendron. This may be a general rule, but it
is by no means a universal one. ‘The size of the leaf-scars on
those so-called Ulodendra is very much influenced by the
extent to which the bark has become longitudinally fissured,
for these clefts act as escapements to the lateral strain (if not
produced by it), which is caused by the increase in girth of
the stem ; whilst in those cases where the bark does not become
fissured, the leaf-scars are laterally expanded by the same
strain which produces the fissuring of the bark.
On specimen No. 1, Pl. IIL. fig. 1, it will be seen that the
leaf-scars have attained a considerable size, and they cannot
be said to be characteristically smaller than those of ordinary
Lepidodendra, nor do they in any point differ in shape or
arrangement from characteristic leat-scars of Lepidodendron
Veltheimianum. It is also to be noted that in this example
the bark is more than usually free from the vertical fissures
* See Zeiller, “ Sur des Cones de Fructification des Sigillaires” (‘Comptes
Rendus des Séances de l’Académie des Sciences,’ 30 June, 1884) ; also
“Cones de Fructification des Sigillaires ” (Ann. des Scienc. Nat. 6° sér.,
Bot. tome xix. p. 256, pls. xi., xil.).
+ I have not entered into the differences in internal structure between
Lepmdodendron, Sigillaria, and Ulodendron. Suffice it to say, that the
internal organization of Lepidodendron and Sigillaria is distinctly dif-
ferent, and that the few specimens of Ulodendron which have been found
with their internal structure preserved apparently agree with Lepido-
dendron.
13*
176 Mr. R. Kidston on the Relationship
which so frequently occur on large Ulodendroid stems. The
leaf-scars on this fossil are, however, larger than they usually
are on most Ulodendroid specimens, such as those figured
by Brongniart *, Allan f, Stur ¢, and Schimper§. When the
leaf-scars are small they are usually more or less distant (spe-
cimen No. 3, Pl. LV. fig. 2) ; but with their increase in size,
the intervening space becomes gradually reduced till the leaf-
sears are contiguous (fig. 1, Pl. III.) or nearly so, as in
Stur’s pl. xxu. fig. 3 0.
The leaf-scars appear to have been somewhat elevated ;
hence, when impressions of the plant are examined, the spaces
intervening between the leaf-scars naturally appear as ridges
running between them. These ridges, when partially flat-
tened over the edges of the leaf-scars by pressure, thus some-
what obscure their upper and lower extremities as well as
the margins of the leaf-scars generally, and cause the vascular
impression to appear as if situated at the extreme upper angle
of the leaf-scar ||. It is this state of the plant that has given
rise to the supposed ‘‘ Lepedophlotos-condition ’’ of Lepidoden-
dron Veltheimianum].
The Ulodendroid scars, in their earlier condition, are also
covered with leaf-scars belonging to the ordinary spiral series
of the stem (see specimens Nos. 3 and 7).
Jn some cases the bark is quite free from longitudinal fis-
sures, as mentioned in the description of specimen No. 2,
where from lateral pressure exerted on the leaf-scars by the
increase in girth of the stem, they are almost rhomboidal.
In Pl. IV. fig. 2 is shown a small portion of the outer
surface of a Ulodendroid specimen. ‘The leaf-scars are dis-
tant, and connected with each other by a narrow flexuous
ridge. This is more fully described in the notes on specimen
No. 8, from which the figure is taken. In fig. 3, Pl. IV.
(specimen No. 4) this character is more marked. In fig. 4,
Pl. IV. is shown a very common form of leaf-scar, occur-
ring both on specimens showing the large Ulodendroid scars
and also on those on which they are not present, as was
* Hist. d. végét. foss. vol. ii. pl. xviii.
+ Trans. Roy. Soc. Edin. vol. ix. pl. xiv.
} Culm-Flora, pl. xxii. (xxxix.) fig. 3.
§ Traité d. paléont. végét. pl. Lxiii.
|| Probably, in attempting to reconcile a Lepzdophloios condition of
Lepidodendron with Lepidophloios, Renault has been entrapped into pro-
ducing a copy of Goldenberg’s figure 6, pl. xvi., on his pl ix. fig. 1, with
the vascular scar at the upper end of the cushion, whereas it should have
been at its lower extremity.
@ See Renault, Cours d. botan. foss. deuxiéme année, p. 10, pl. v.
fig. 1.
of Ulodendron to Lepidodendron, ce. 177
the case with the example from which this sketch was made.
This figure illustrates the form of the leaf-scar to which
Géppert applied the name of Lepidodendron (Sagenaria)
ellipticum *.
The fissures in the bark do not appear to have ever become
filled with a subsequent development of tissue, but to have
remained as open gashes, for of the numerous émpres-
sions of these plants which have come under my notice,
in every case these clefts were represented as elevated ridges
on the surface of the impression, or as fissures in the bark ;
hence they must have been open clefts at the time of minera-
lization. Nor do these clefts appear to have been caused by
shrinkage or breakage of the bark after the plant was im-
bedded in the material which now forms its matrix; for had
it been brought about by any secondary cause, we should
expect to find these clefts in the bark of all Lepidodendra,
which we do not.
But, on the other hand, all Lepidodendroid Ulodendra do
not show this peculiar character of the bark becoming split,
for I have seen specimens, some of them very large, of a
Lepidodendroid Ulodendron from the Scotch Coal-Measures f,
in whose bark, in only one case, was there a slight and indi-
stinct indication of these vertical clefts. Therefore, although
perhaps of specific value, I am not inclined to regard the
longitudinal fissuring of the bark as of generic importance.
From many specimens of these so-called Ulodendra (Ulo-
dendron parmatum, Carr.= U. commutatum, Schimper, &c.),
some of which I figure (figs. 1-2), portions of the stems had
been broken off, either trom the sides of the fossils or from
between the scars; such pieces could not have been distin-
guished from Lepidodendron Veltheimianum, Sternberg, with
which they entirely agree.
Sigillaria discophora, Konig, sp.
I have given on Pl. IV. fig. 7, a copy of a few leaf-scars
of Sigillaria Brardii t, for comparison with those of this and
the following species.
The leaf-scars (a, fig. 7) of Sigillarta Brardit are placed
on more or less elevated cushions (g, fig. 7). These cushions,
as in Lepidophloios, are morphologically distinct from the leaf-
structure, and belong to the cortical envelope, being portions
of it, in fact, only mamilliform protuberances. Superficially
* Foss. Flora d. Uebergangsgebirges, pl. xliii. fig. 7.
t+ From Rosewell Colliery, Midlothian, and Bonnington Pit, Kilmar-
nock, Ayrshire.
} From Brongniart’s Hist. d. végét. foss. pl. clviii. fig. 4.
178 Mr. R. Kidston on Ulodendron.
these cushions more or less exceed in area the surface to
which the leaf is articulated, and have a casual resemblance
to the “ field’ in Lepidodendron, but with this they have no
real relation. In Lepidodendron the leaf-base is attached to
the “field”’ (ec, fig. 15) as well as to the vascular scar; in
Sigillarta, on the other hand, it is only attached to the
vascular scar.
I now hope to show that in Stgillaria discophora, Kénig sp.
(=U. majus, L. & H., and U. minus, L.& H.), and Ulodendron
Taylort, Carruthers, the leaf-scar agrees in all essential points
with those of the Clathrarian Sigillarie, of which I have taken
Sigillaria Brardii, Brongniart, as the type. In fig. 12, Pl. VII.
(specimen No. 12), a great diversity is seen in the form of
the leaf-scar. Immediately beneath the Ulodendroid scar
the leaf-scars are of the Stgil/aria-Brardii type. ‘These are
enlarged in fig. 12@, Pl. VII. They are rhomboidal, their
upper and lower angles rounded, and their lateral angles pro-
duced and prominent; the leaf-scars are also placed upon
slightly elevated cushions, and though the cushion is not
much larger than the vascular scar, its presence is clearly
observable. ‘The small cushions on which the leaf-scars sit
are well seen in Pl. V. fig. 8. This, I think, proves the
structural identity of the leaf-sear of Stgillaria discophora,
Konig, sp. (= Ulodendron majus, L. & H.), with that of the
Clathrarian group of the genus S¢gillaria.
I have not met with any specimens of Sigzllaria discophora
which clearly show the vascular-bundle cicatricules ; but such
have been figured by Sir William Dawson under the name of
Lepidophloios parvus*, where they are represented as of the
ordinary Sigillarian type, with three vascular-bundle “ dots,”
the central punctiform and the two lateral lunate. At the part
marked 6, fig. 12, Pl. VII. (specimen No. 12), and enlarged
at fig. 12 6, the scars assume a quadrangular form and usually
show acentral “dot.” Fig. 13a, Pl. VII., gives a few leat-
scars, natural size, from fig. 13 (specimen No. 14). This
form of leaf-scar, arising from the age of the specimen, and
perhaps also from changes which have taken place during
mineralization, has given rise to Dawson’s Lepidophloios
tetragonus tT. ‘The fact of this form of leaf-scar occurring on
the specimen represented in fig. 12, Pl. VII., along with the
ordinary leaf-scars of the species, proves conclusively the
identity of Lepidophlotos tetragonus, Dawson, with Sigillaria
discophora, Koénig, sp. On some specimens of this species,
especially the older and larger ones, the bark also becomes
* Acadian Geol. 2nd ed. p. 455, fig. 170 Ga.
y+ L.c. p. 456, fig. 170 p.
Mr. H. J. Carter on Meyenia fluviatilis. 179
fissured as in Lepidodendron Veltheimianum; this is seen in
the fossils illustrated in figs. 5 & 13, Pls. IV. and VII.
Sigillaria Taylort, Carruthers, sp.
In form the leaf-scars in this species are essentially of
the same type as those occurring in Stgillaria discophora,
Kénig, sp. They are small and seldom occur in so good a
state of preservation as to give a clear idea of their form. I
have, however, succeeded in securing several examples which
afford the necessary details on this point. In fig. 6, Pl. IV.
(specimen No. 16), the form of the leaf-scars is well seen. It
is remarkable that on one small part of this fossil they should
be so well preserved, and on all the rest of its surface be com-
pletely effaced. The upper and larger Ulodendroid scar
appears to have been displaced.
The leaves of this and the previous species seem to have
remained attached to the stem for a considerable time, and
very often their being buried in the matrix appears to have
given the outer layer of the bark a tendency to adhere to the
impression side of the slab when the stones were split; when
this happens there is presented to our view the form of the
leaf-scars as seen on the ¢nner surface of the outer layer of the
bark. This condition is exhibited at the part marked 4,
fig. 10, Pl. VI., which is shown of the natural size in fig. 100.
Fig. 12, Pl. VII., shows a like state of preservation.
At various parts of the specimens of Stgillaria discophora
and Stgillaria Taylori are shown their decorticated conditions,
for which Lindley and Hutton founded the genus Bothro-
dendron (Pl. VII. fig. 13 6, and Pl. VI. fig. 10 d).
[To be continued. |
XIX.—On a Variety of the Freshwater Sponge Meyenia
fluviatilis, auctt., from Florida. By H. J. Carrer, F.R.S.
&e. :
Next to Mr. Ed. Potts, of Philadelphia, comes Mr. Henry
Mills, of Buffalo, in the discovery of freshwater sponges in
his particular locality, and in the praiseworthy desire to
advance the subject by sending specimens of them to Kuro-
pean as well as American naturalists. Of the species in the
Niagara River Mr. Mills has long since forwarded to me
180 Mr. H. J. Carter on Meyenia fluviatilis.
several handsome specimens for distribution among the
museums in this country, and proposes to send more; hence
J have already been able to enrich the collections of Spongille in
the British and Liverpool Museums respectively to this extent.
Not confining his researches to the Niagara River, Mr.
Mills has also not forgotten the subject when abroad, although
engaged in other matters probably of more importance, so
that during his last two visits to Florida he has been almost
equally successful there in his discovery of the freshwater
sponges, and equally generous in sending about specimens of
them on his return to Buffalo. One of them, which he has
kindly sent to me, he has, at my suggestion, designated a
variety of Meyenta fluviatilis, under the name of ‘ gracilis,”
and this, from his accompanying data, together with two
slides and a bit of the sponge itself in spirit, I shall, at
his request, presently describe for publication; the rest, m-
cluding his Meyenta Everett’, from Massachusetts, will
probably appear in Mr. Potts’s forthcoming Monograph of
the freshwater sponges of North America.
Meyenia fluviatilis, var. gracilis.
Delicate in structure, which is soft, whitish or colourless in
spirit, presenting the aspect of glue or sarcode when dry;
growing over the stem of an aquatic plant in a thin layer
charged beneath with statoblasts (gemmules). Spicules of
two forms, viz.:—1, skeletal, very fine and delicate, acerate,
curved, cylindrical, about 84 to 36 by 4-6000th inch in its
greatest dimensions, chiefly confined to the fibre; 2, stato-
blast-spicule, shaft long, cylindrical, often slightly curved,
smooth, also very thin and delicate; head small, flat, radiately
denticulated, the ends of the rays not recurved; often
umbonated by a projecting spine or process, total length
about 7-6000ths inch, head 14-6000ths inch in diameter, ©
shaft about five times longer than the diameter of the head,
about +-6000th inch thick ; chiefly confined to the statoblast,
but also loose and numerous in the tissue generally. Stato-
blast globular when wet, hemispherical and depressed in the
direction of the aperture when dry ; when fully formed about
65 to 75-6000ths inch in diameter. Aperture slightly mar-
ginated, 7. e. slightly raised above the common level, about
8-6000ths inch in diameter. Surface of statoblast rough or
uneven. In a section through the centre the crust is seen to
be a little thicker than the length of the birotules, which, as
usual, are arranged perpendicularly to the yellow chitinous
coat beneath and parallel to each other, with one head resting
On the ‘Challenger’ Cephalopoda. 181
on the chitinous coat and the surface of the other free at the
circumference ; cemented together and held in position by the
microcell-structure or “‘ float,’ which, projecting above the
level of the outer heads of the birotules, gives rise to the
roughened state of the surface of the statoblast. Chitinous
coat and germinal contents the same as in the Spongille
generally. Size of specimen sent to me about 41x32 inch
horizontally.
Hab. Fresh water.
Loc. “ Ice-Factory Lakes, De Land, Florida, near the St.
John’s River.”
Obs. The extremely delicate character of the spiculation
generally, the microspined skeletal spicules, the great length
of the birotules, and the radiating portions of the head being
horizontal and not recurved at their extremities, allies this
species more to Meyenia fluviatilis than to the Heteromeyenie —
(e. gr., Spongilla Baileyi, Bk., Proc. Zool. Soc. 1863, pl.
xxxvill. fig. 6) of Mr. Potts. Hence the name.
XX.—Diagnoses of new Species of Cephalopoda collected during
the Cruise of H.M.S. ‘Challenger.—Part Il. The Decapoda.
By Wituram HE. Horie, M.A. (Oxon), M.R.C.S.,
F.R.S.E., Naturalist to the ‘ Challenger’ Commission.
[Published by permission of the Lords Commissioners of H.M.
Treasury, and extracted from a paper read before the Royal Society of
Edinburgh, July 6, 1885.
Myopside.
PROMACHOTEUTHIS, Hoyle.
Promachoteuthis, Hoyle, 1889, Narr. Chall. Exp. vol. i. p. 278, fig. 109,
The Body is short, rounded, with large broad jins, situated
posteriorly. The mantle is free behind, as in Rossia. The
siphon is short and slender and with everted margin ; valve?
The Head is small and narrow ; eyes not prominent.
The Arms are long and conical, with two series of pedun-
culate spherical suckers. The tentacles exactly resemble the
arms at their origin ; the club is absent.
The Gladius has not been removed from the single example.
182 Mr. W. E. Hoyle on the
Promachoteuthis megaptera, Hoyle (loc. ctt.).
The Body is short, barrel-shaped, rounded behind ; the fin
is large, transversely elliptical, and extending beyond the end
of the body posteriorly ; each half is wider than long. The
mantle-margin is transversely truncated. The mantle-con-
nective consists of a linear ridge on either side, fitting into an
almond-shaped depression at either side of the base of the
siphon, which is short, slender, and has the distal margin
everted, like the neck of a flask; the specimen was so small
and indifferently preserved that it was not opened to ascertain
whether a valve was present.
The Head is very small and narrow, almost the whole of
its sides being occupied by the eyes, which are not prominent,
but covered with a transparent membrane, and with a distinct
pore in front of and below each.
The Arms are unequal, the fourth being the shortest (con-
siderably so on the right side); the first, second, and third
are subequal ; they are on an average about the same length as
the body, smoothly conical, and tapering evenly to fine points.
The suckers are in two series throughout, pedunculate,
spherical, with a lateral aperture directed inwards ; the horny
ring is smooth and surrounded by a few large papilla. The
hectocotylus is not developed. ‘There is no trace of an wm-
brella. The buccal membrane is weil developed and has the
usual seven points, but they are not very well marked or
provided with suckers ; the membrane is not connected with
the arms by ligaments. There seems to be only one hp,
which is thick and papillate.
The Tentacles arise directly between the third and fourth
arms, exactly resembling them at their origin, and obviously
being part of one series with them ; the stem is swollen at first
and somewhat more than one third up the arms narrows rather
suddenly to about half its previous diameter. The club is
wanting.
The Surface is smooth.
The Colour is a dull purplish madder, paler on the fins
(especially their under surface) and on the arms and tentacles.
The Gladius has not been extracted.
Hab. North Pacific, east of Japan (Station 237), 1875
fathoms. One specimen, sex ?
Loxieo, Lamarck.
Loligo ellipsura, n. sp.
The Body is elongated, widest anteriorly, and tapering
‘Challenger’ Cephalopoda. 183
gradually to an acute point behind. The fin is comparatively
short, only one third the length of the body, elliptical, slightly
broader than long. ‘The mantle-margin passes almost straight
across the back, except where a long narrow median process
juts out over the head ; it is slightly sinuate ventrally. The
siphon is short and blunt.
The Head is short and very nearly as broad as the body;
it has the usual auricular crest and pre-ocular pore.
Lhe Arms are unequal, the order of length being 3, 4, 2,1,
and about one third the length of the body; the first has a
distinct web on its dorso-median angle, and the third a still
broader web on its outer aspect, passing back nearly as far
as the eye, where it becomes connected with another passing
up the dorso-lateral aspect of the fourth. The suckers are in
two series, pedunculate, oblique, notched distally, and some-
what larger on the lateral than on the other arms. The
horny rings bear from five to seven large pointed teeth in
their distal portion, but are smooth proximally. The hecto-
cotylus is not present. The buccal membrane has the usual
seven points, each of which carries two or three small suckers.
The outer lip is thick and marked with radial grooves; the
inner lip was not seen.
The Tentacle is slender, approximately cylindrical, and
about two thirds the length of the body; its terminal fourth
is occupied by the club, which is but little expanded, and has
a delicate protective membrane along either side of the inner
surface and a well-marked web externally. The large median
suckers are about ten in number, and about twice as large as
the alternating lateral; the proximal are about twenty, and
gradually increasing ; the distal occupy nearly one half the
club, and are in four series diminishing. The horny rings of
the largest suckers have about twenty-four distant square
pointed teeth, much longer on the distal margin; the lateral
ones have about half as many similar teeth on the outer
margin, and the terminal suckers are armed in the same way.
The Surface has been almost entirely denuded of skin.
The Colour appears to have been pale buff with purple
chromatophores. .
The Gladius has not been extracted.
Hab. Off Sandy Point, South America (Station 313),
do fathoms. One specimen, apparently ¢.
Loligo galathee, Steenstrup, MS.
The Body is about three times as long as broad, cylindrical
anteriorly, and pointed behind. The jim is rather less than
184 Mr. W. E. Hoyle on the
half the length of the body *, about as long as broad, and
with rounded lateral angles. The mantle-margin curves out
rapidly to a triangular process in the dorsal median line, for
the rest is almost transverse, except where it forms two obtuse-
angled processes, one at either side of the ventral margination.
The Head is comparatively broad and with prominent
rounded eyes. The siphon is moderately large and of the
usual form.
The Arms are unequal, the order of length being 3, 4, 2, 1,
and not quite one third as long as the body. The dorsal
have a distinct keel on the upper margin, the second are
keeled on the ventro-lateral aspect, the third are stout and
flattened and have a broad web on the outer aspect, which
unites with the web running up the dorso-lateral aspect of
the ventral arms. ‘he suckers are in two series throughout,
with short peduncles, and not very oblique; their horny
rings bear nearly twenty distant blunt teeth. The hecto-
cotylus is not developed. The umbrella is absent. The
buccal membrane has the usual seven points, each of which
bears a few suckers. The outer lip is thin, the dnner thin
and papilate.
The Tentacles are comparatively short, being not quite so
long as the body; the stems are subtriangular. The club
occupies more than one third of the length, and has a pro-
tective membrane at either side of the suckers and a distinct
web on the outer aspect. The large central suckers are from
eight to ten in number, and nearly twice the diameter of the
lateral ones ; the proximal group consists of about ten, while
the distal portion bears four series of diminishing suckers. The
horny ring bears long, distant, bluntly pointed teeth, about
twenty-four in the largest suckers, proportionally fewer in
the smaller, which are much larger in the distal and external
portions of the ring respectively.
The Surface is smooth. .
The Colour is pale yellowish, spotted with brownish-
purple and red chromatophores.
The Gladius has not been removed.
Hab. Philippine Islands (Station 203), 20 fathoms. ‘T'wo
specimens, Juv.
Loligo kobiensis, n. sp.
The Body is elongated, cylindrical in the anterior moiety,
* With respect to this and one or two other points in the description
it must be remembered that the specimens are immature.
‘Challenger’ Cephalopoda. 185
then tapering posteriorly, and terminating in a blunt point.
The jin is more than half the length of the body, trapezoidal,
with rounded lateral angles; the extreme breadth is less than
the length and is situated anteriorly to the middle of the fin.
The mantle-margin presents a triangular process in the mid-
dorsal line and is deeply sinuate ventrally. The sdphon is
short and bluntly conical.
The Head is short and not so broad as the body; the eyes
are comparatively small and have a bracket-shaped auricular
crest behind and a minute pore in front of them.
The Arms are unequal, the order of length being 3, 4, 2, 1,
and, on the average, rather more than one third the length of
the body ; the first are the most slender, and have the dorso-
median angle raised into a prominent keel; the second have
only a faintly-marked angle ventro-laterally.; the third have
a broad web externally, passing over at the base into one
which extends up the dorsal aspect of the lateral arms. The
suckers are arranged in two series, pedunculate, very oblique,
and rather larger on the lateral than on the other arms; the
horny ring has about nine short, close-set, square-cut teeth
on its distal side, and is smooth on the proximal. The hecto-
cotylus was not observed. The buccal membrane has five
points, each of which bears two or three small suckers;
the two ventral points are rounded off; just within the ventral
margin is a smail papilla surrounded by two elevated rings,
probably for the reception of spermatophores. Both the outer
and inner lips are folded.
The Tentacle is faintly three-sided and shorter than the
body, one third of its length being taken up by the club,
which is expanded and triangular in section; there is a pro-
tective membrane on either side and a web externally ; in the
centre are eight large suckers, three times the diameter of the
lateral ones; at the proximal end are about nine suckers,
gradually increasing in size, and at the distal end more than
twenty rows arranged in four series, gradually diminishing.
The largest suckers are scarcely at all oblique, and have the
margin cut up by radial grooves into a number of small
papillz, an arrangement also found on the outer margin of
the lateral suckers, but not in the terminal ones. The horny
rings of the largest suckers are smooth ; those of the lateral
bear about twelve long distant teeth on their outer margin ;
those of the terminal suckers are similarly armed.
The Surface is smooth.
The Colour is pinkish yellow, with purplish chromato-
hores.
The Gladius has not been extracted.
186 Mr. W. E. Hoyle on the
‘Hab. Off Kobi, Japan, 8 fathoms; one specimen, 2.
South of Japan (Station 233 c), 11 fathoms ; two specimens,
juv. Also (?) Inland Sea, Japan; two specimens, juv.
Loligo edulis, n. sp.
The Body is moderately stout, being about three times as
long as broad, cylindrical in its anterior third, and tapering
gradually to a bluntish point. The fim occupies a little more
than half the length of the body, rhomboidal, not quite so
broad as long, and broadest anteriorly to the middle; the lateral
angles are rounded. The mantle-margin has a slight pro-
jection in the median dorsal line and a broad shallow sinuate
excavation ventrally. The siphon is of moderate length and
bluntly pointed.
The Head is small, with prominent rounded eyes, and bears
the usual auricular crest and preocular pore.
The Arms are vnequal, the order of length being 3, 4, 2, 1,
and about half as long as the body. ‘The first are very
slender and bear a distinct keel on the dorsal aspect; the
second are thicker and triangular, and have a broad keel
almost expanding into a web on the lateral aspect; the third
are the stoutest, flattened from above downwards, and di-
stinctly keeled externally ; the fourth are intermediate between
the third and second, triangular, and with a broadish web
extending the whole way up the dorso-lateral aspect. They
all have a web up each side of the inner face. ‘The suckers
are in two series, very oblique, and with slender conical
peduncles, their size varying with that of the arms on which
they are situated ; the horny ring bears eight long square-cut
teeth on its distal margin. The hectocotylus is developed as
usual on the left ventral arm, which bears proximally ten
rows of suckers, then a minute sucker with an exaggerated
peduncle, and beyond this two series of long conical papille.
The buccal membrane has the usual seven angles produced
into long lappets, each of which bears about eight suckers in
two rows; the outer lip is moderately thick; the crner lip
much thicker and marked with deep radial grooves.
The Tentacles are about as long as the body, with flattened
stems; about one third their length is occupied by the elud,
which is only slightly expanded, and has a protective mem-
brane on either side, but a dorsal web is present only at the
extremity. The central suckers are about sixteen in number
and about one third larger than the Jaterals; the proximal are
about ten; the distal are closely packed in four series. The
horny rings of the largest are provided with about twenty
‘Challenger’ Cephalopoda. 187
larger teeth, with which smaller ones alternate somewhat
regularly; the lateral bear about ten distant acute teeth on
the outer margin, while the proximal and distal groups are
similarly armed on the distal margin.
The Surface is smooth.
The Colour is a dull yellow with purplish chromatophores.
The Gladius is of the usual form, the narrow anterior
portion being less than one fourth of the total length.
Hab. Japan; purchased in the market, Yokohama. One
specimen, ¢.
Loligo japonica, Steenstrup, MS.
The Body is only moderately elongated, being about three
times as long as broad, and bluntly pointed behind. The
jin is a little more than half the length of the body, about
as long as broad, rhomboidal, rounded laterally, and very
slightly notched. at the anterior angles. The mantle-margin
curves gradually forward to a projecting point in the dorsal
median line, and is deeply emarginate ventrally. The sephon
is short and of the usual form.
The Head is comparatively large and rounded; the eyes are
swollen and prominent.
The Arms are unequal, the order of length being 3, 4, 2,1,
and on an average about half as long as the body; the first
are very small, slender, and rounded; the second have a
prominent ventro-lateral angle, not amounting to a keel; the
third have a distinct web on the outer aspect of the distal
portion, which is continued backwards as a faint ridge which
joins the web lying along the dorsal lateral edge of the fourth.
The suckers are in two series, and vary in size in accordance
with the arms on which they are situated ; they are subglobular
and oblique. The horny ring bears about ten broad, close-
set, square-cut teeth. ‘The hectocotylus is present on the left
ventral arm; the distal suckers of the ventral series only are
modified into conical papillae, some of which bear a minute
sucker at their tips. The wmbrella is absent; the buccal
membrane is well developed, has the usual seven points, each
of which bears a few small suckers (occasionally only one).
The outer lip is thick, thicker than the ¢mner; both are cut
up into papille along the edge.
The Tentacles are as long as the head and body together,
and have very slender, almost cylindrical stems; the club
occupies about one fourth of the whole length, and is but
slightly expanded. The large central suckers are about eight
in number and fully twice the diameter of the lateral ones ;
188 Mr. W. E. Hoyle on the
proximally to them are about half a dozen suckers of different
sizes, and beyond them a large number of diminishing ones
arranged in four series and occupying nearly half the length
of the club. The horny ring in the largest suckers bears
about twenty-five square teeth ; in the lateral suckers it bears
more than twenty close-set bluntly pointed teeth, and in the
distal ones about the same number of similar character.
The Surface is smooth.
The Colour is pale, with purplish chromatophores.
The Gladius is of quite typical form, expanded behind, and
about six times as long as broad; the narrow anterior extre-
mity occupies less than one third of the total length.
Hab. Japan; purchased in the market at Yokohama. One
specimen, ?.
Sepia, Linné.
Sepia esculenta, n. sp.
The Body is broad, stout, and semielliptical posteriorly.
The fins are about one fourth of the body in breadth and
commence within 6 millim. of the anterior margin, and end
within 5 millim. of each other; the mantle-margin is pro-
duced far over the head dorsally, and evenly truncated below.
The s¢phon just reaches the gap between the ventral arms.
The Head is broad and the eyes laterally prominent.
The Arms are subequal, the order of length being 4, 1, 2,3,
and nearly half as long as the body; they are all more or less
compressed, especially the ventral ones ; they have a distinct
web along the outer margin, and a rather broad membrane.
runs up either side of the sucker-bearing face. The suckers
are in four series throughout, not very obliquely set; they
are large and spheroidal, and have meridional markings on
the outer surface ; the horny ring is smooth and surrounded
by a narrow papillate area. In the hectocotylized arm of the
male the first four rows of suckers are normal, then come’ two
rows of gradually diminishing suckers, succeeded by four
rows of minute ones, after which they regain their normal
dimensions. The umbrella is narrow, widest between the
second and third arms, where it reaches up to the fifth row
of suckers. The buccal membrane has the usual seven points
in the male; in the female the two ventral ones are rounded
off; the spermatic cushion is exceedingly well developed, and
has four deep transverse grooves. The owter lip is thin and
longitudinally corrugated; the inner lip is thick and bears
numerous very long papille.
_ ‘Challenger’ Cephalopoda. 189
The Tentacles are absent.
The Surface is smooth throughout.
The Colour is dull grey, mottled with black above, yellowish
below.
The Shell is elliptical in outline, somewhat broader behind
(especially in the female); the chztiénous margin is narrow
and does not form a complete ridge across the shell below
the spine ; it forms two slightly expanded wings behind, and
extends but a little distance over the dorsal surface, which is
marked with coarse rugosities disposed in curved lines
parallel to the anterior margin; a distinct but low rib runs
down the centre. The ventral surface is elevated on either
side of a deep median groove; the last loculus covers about
one fifth of the surface, and is bounded posteriorly by two
slightly wavy lines, meeting at an acute angle; the striated
area 1s long, and the angle between the striz widens poste-
riorly. The inner cone is very well developed; the limbs
arise one fifth of the length of the shell forward, and gradually
become more elevated until they enclose a deep conical cavity.
The spine is strong, pointed, and somewhat curved laterally
in the female example.
Hab. Japan; purchased in the market at Yokohama. ‘Two
specimens, 1 ¢, 1 ?.
Sepia elliptica, un. sp.
The Body is ovoid, broadest one third from the anterior
margin, pointed behind. The fins are one third the width of
the body, broadest in the middle, extending the whole length of
the body, and approaching within 2 millim. of each other
posteriorly. The mantle-margin not very prominent over
the head dorsally. The mantle-connective is rather short and
deep, but otherwise normal. The s¢phon is conical, reaching
within 1 millim. of, or quite up to, the space between the
ventral arms.
The Head is very short and broad, the eyes prominent.
The Arms are subequal, the order of length being 4, 3, 2,
1; they are nearly half the length of the body, and taper
evenly to fine points; there is a distinct but narrow ridge
along the fourth and a delicate web along each side of the oral
aspect of the arms. ‘The suckers are in four series throughout,
and of moderate size, marked with inconstant meridional
grooves, and there is a large notch proximally and distally in
the rim. The horny ring has for the most part no distinct
teeth, but is marked in the distal half with shallow irregular
notches, which are occasionally more regular. A papillary
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 1
190 Mr. W. E. Hoyle on the
area surrounds the horny ring. The hectocotylus is developed
in about the middle third of the left ventral arm; beyond the
eighth row of suckers the two ventral series are continued of
the normal size, but the two dorsal are each represented by
five minute suckers, gradually diminishing to the middle one
and then increasing again; beyond this the arm exhibits
no peculiarities. The umbrella is widest between the two
lateral arms, where it extends as far as the sixth row of
suckers. The buccal membrane bears the usual seven distinct
points in the male, whilst in the female the ventral pair are
lost in the thick swollen spermatic cushion; this is subdivided
by four or five deep grooves into as many transverse ridges.
The outer lip is thin; the ¢nner bears about half a dozen rows
of distinct hemispheroidal papille.
The Tentacles are about as long as the mantle; the stem is
indistinctly three-sided ; the club is long and wide, and bears
eight series of minute equal suckers; there is a protective
membrane on either side and a broad jin on the dorso-internal
aspect. The horny ring is small and has a smooth margin.
The Surface is smooth.
The Colour is a dull grey dorsally, pale yellowish below.
The Shell is broad, subelliptical in outline, the anterior
extremity bounded by two straight lines, which form obtuse
rounded-off angles with each other and the sides of the shell ;
the posterior is rounded gradually off. The dorsal surface
has a faint ridge passing to each of the three angles just
mentioned, and is covered with curved rows of tubercles
parallel to the anterior margin. The ventral surface is but
little elevated ; the last loculus occupies one third of it, and is
bounded behind by a broadly open curve with three or four
irregular sinuations in it. The striated area is hollowed
posteriorly and is marked by grooves corresponding to the
sinuations just mentioned. ‘The ¢nner cone arises about half-
way along the striated area, curves evenly outwards, and then
rises into a distinct ridge, forming a wall separate from the
margin of the shell ; its ventral surface is marked by a num-
ber of striz pointing in the direction of the spine, which is of
medium length and strength, and curved gently upwards.
Hab. South of Papua (Station 188), 28 fathoms; four
specimens, 1 g¢,3 9. Also Station 190, 49 fathoms; four
specimens, 1 ¢,3 9.
Sepia Smitht*, n. sp.
The Body is of medium breadth, widest one third back,
* Named after Mr. Edgar A. Smith, F.Z.S., of the British Museum.
‘Challenger’ Cephalopoda. 191
curving evenly to a pointed posterior extremity. The fin is
nearly one third the breadth of the body, extending from the
anterior margin of the mantle to within 4 millim. of its fellow
at the posterior extremity. ‘The mantle-margin projects to a
considerable extent over the head dorsally, and is slightly
emarginate ventrally. The siphon is long, reaching up to
the interspace between the ventral arms.
The Head is of medium breadth and the eyes prominent.
The Arms are subequal, their order of length being 4, 3,
2,1; they are a little more than half as long as the body;
the dorsal are the smallest and subconical, the ventral wide
and with a narrow web on the outer aspect; they all taper
gradually to fine points. The suckers are in tour series
throughout, pedunculate, oblique, and notched proximally
and distally, and with meridional grooves on the margin; the
horny ring has about twenty blunt triangular teeth on the
distal semicircumference, and is surrounded by a broad papil-
late area. The hectocotylus is not present. The umbrella is
but slightly developed, reaching in its greatest extent (between
the third and fourth arms) only to the fourth row of suckers.
The buccal membrane has the usual seven points, but there ig
no spermatic cushion. ‘The outer lip is moderately thick and
longitudinally ribbed; the cner is provided with many rows
of elevated rounded papille.
The Tentacles are about as long as the mantle, and have
stout three-sided stems; the club occupies about one fourth of
the whole length, and extends fully half round the stem; a
protective membrane is found at either side of them and a web
along the dorso-median aspect of the club. The suckers are
very numerous, minute and closely packed; the horny ring has
about eight or ten stout distant teeth on the distal margin.
The Surface is for the most part smooth, but there are
about five elongated elevations down each side of the body
near the origin of the fin, and a few minute papille on the
dorsal surface.
The Colour is a dull purplish grey above, pale ochre
below.
The Shell is roughly elliptical in outline; the anterior
extremity is bounded by two straight lines forming a blunt
rounded angle; the sides curve evenly outwards (the greatest
breadth being a little anterior to the middle) and form a
bluntish point behind. The chitinous margin is narrow and
vanishes in the median ventral line behind. The dorsal sur-
face is rough, with granules arranged in rows parallel to the
anterior margin ; three slightly elevated tracts diverge from
the spine to the three anterior angles. ‘The aa surface
14%
192 Mr. W. E. Hoyle on the
is little elevated ; the last lJoculus occupies one fourth of the
length, and is emarginate, being bounded behind by a more
or less evenly curved line; the striated area is exca-
vated, so that the whole shell is thin; the ¢nner cone is well
developed, with a thickened rounded margin, and encloses a
deep pit; the limbs extend halfway along the striated area.
The spine is long, tapering, and curves gently upwards.
Hab. South ot Papua (Station 183), 28 fathoms. Four
specimens, ?.
Sepia sulcata, n. sp.
The Body is cylindrical in its anterior fourth, then tapering
gradually backwards, and pointed behind. ‘The jins are one
fifth the breadth of the body, commence 2 millim. from the
anterior margin of the mantle, and approach within 5 millim.
of each other posteriorly ; the mantle-margin reaches far over
the head dorsally, and is evenly truncated below. The sephon
does not extend up to the interbrachial space.
The Head is broad and the eyes very prominent; in the
only specimen it is much retracted into the mantle.
The Arms are subequal, the order of length being 4, 3,
2, 1; they are one third the length of the mantle, and taper
gradually to slender points; the first are thin and rounded,
the fourth flattened; each has a distinct ridge on the outer
side, which in the fourth expands into a broad membrane.
The suckers are in two series in the first and second arms, but
with a tendency to form four series in the others, more espe-
cially in the distal portions ; they are pedunculate and very
oblique, and the margin is marked with meridional grooves
and has a deep distal notch; the horny ring is small, smooth,
and surrounded by a papillate area. ‘The hectocotylus is
present along three fourths of the left ventral arm in the
form of a groove with convex bottom, bounded on either side
by a narrow fillet; on either margin of the groove is a row of
minute suckers, which are larger and more distinct, and even
form two series on the ventral aspect; the tip of the arm
bears two series of small suckers. The umbrella is better
developed than usual, its greatest extent (between the lateral
arms) being up to the eighth row of suckers. The buccal
membrane has the usual seven points, but not very strongly
marked ; the outer “ip is smooth and thin, the ¢nner papillate.
The Yentacleis as long as the head and body together, with
a slender and somewhat flattened stem; the club is short and
rather broad, and has a protective membrane on either side of
the suckers, and a broad web on the dorsal aspect, extending
‘Challenger’ Cephalopoda. 193
for a distance equal to half its length down the stem : there
are from six to eight rows of very minute suckers, subequal,
and with smooth horny rings.
The Surface is smooth, except that on one side of the
ventral surface are three slightly raised linear ridges, appa-
rently due to contraction, and a few minute papille on the
dorsal surface posteriorly.
The Colour is on the whole pale, yellowish below, purplish
above.
The Shell is hemielliptical in outline anteriorly, tapering
to a point behind. The chitinous margin is rather broad,
widest about two thirds back ; it covers all except the median
third of the dorsal surface, which is finely rugose where free,
and has a slightly elevated median portion and a faint linear
ridge in the middle line posteriorly, about 3 millim. long, and
terminating 2 millim. from the base of thespine. The ventral
surface is but little elevated ; the last loculus occupies more
than one third of it, and its posterior boundary is almost
semicircular, inflected in the centre. The inner cone is eva-
neseent ; its limbs are chitinous and form a ventral margin to.
the terminal cone. A spine is present, but, as it had been
broken off, its length and form cannot be determined.
Hab. Off the Ki Islands (Station 192), 140 fathoms. One
specimen, ¢.
Sepia andreanotdes, n. sp.
The Body is very long, broadest one third of the way back,
pointed and acuminate behind. The fins are narrow, com-
mence 3 millim. behind the anterior margin, and terminate
5 millim. from the posterior end of the body, and passing
on to the dorsal aspect of the body, each approaches within
3 millim. of its fellow. The mantle-margin extends well
over the head dorsally, and is very slightly emarginate ven-
trally. The s¢phon extends rather further forward than the
middle of the eyes, but not up to the space between -the
ventral arms.
The Head is decidedly narrower than the body and some-
what elongated ; the eyes being distended and laterally pro-
minent.
The Arms are subequal, the order of length being 1, 2, 3,
4, or 1, 4, 3, 2; they are two fifths the length of the body,
elongated, conical (except the fourth pair, which are flattened),
and taper to very slender tips. ‘The suckers seem to be nor-
mally in four series, but in some cases the arms are so com-
pressed that they seem to be in only two, especially at the
proximal extremities of the first and second arms; they are
194 Mr. W. E. Hoyle on the
globular, slightly oblique, with a small aperture and smooth
horny ring. The hectocotylus occupies the distal half of the
left ventral arm; the suckers are normal up to the twelfth
row, after which the arm widens and has a median groove
from which about twelve shallow grooves pass outwards on
either side, separating raised portions, each of which bears a
minute sucker on the dorsal side of the groove. ‘The wmbrella
is present only between the second and third and third and
fourth arms up to the fourth row of suckers. The buecal
membrane is well developed and has the usual seven points ;
im the female there is a thick deeply grooved spermatic
cushion. The outer ip is thin and smooth, the énner thick
and ‘papillate.
The Tentacles are somewhat longer than the head and
body, very slender and somewhat flattened. The club is
flattened and expanded; along its outer margin is a very
narrow membrane, and along the median edge, at some dis-
tance from the cupules, is a broad web, marked on the dorsal
aspect with fine parallel shallow oblique grooves; along one
margin it bears three or four series of small pedunculated
suckers, whose horny rings bear very numerous and acute
teeth. :
The Surface is smooth.
The Colour is a dull purplish grey above, ochre with purple
chromatophores below.
The Shell has a narrow elongated oval outline, somewhat
pointed in front and tapering gradually backwards ; the chit-
nous margin extends about one third across the dorsal surface,
which shows-the boundary lines of the loculi clearly as brown
strie, and is very minutely roughened: the ventral surface
is elevated, so that the shell is thick in proportion to its
breadth, a narrow groove runs down the centre: the last
loculus occupies one fourth of the surface and is bounded poste-
riorly by a shallow open curve. The posterior extremity is a
very flattened irregular cone, to the apex of which the spine
is attached; the inner cone is very shallow and its opening
is some 4 millim. from the margin of the outer cone. The
spine is long, straight, and points directly backward.
Hab. Japan; purchased in the market at Yokohama.
Three specimens, 1 5,22.
Sepia kiensis, nu. sp.
The Body is narrow, widest anteriorly, and tapering gradu-
ally backwards : the jim is narrow, less than one quarter the
breadth of the body, widening a little behind ; it commences
‘Challenger’ Cephalopoda. 195
1 millim. from the anterior margin and extends to within
2 millim. of its fellow behind. The mantle-margin is pro-
minent dorsally and slightly emarginate ventrally. The
siphon does not quite extend to the bases of the arms.
The Head is broad, and the eyes rounded and prominent.
The Arms are subequal, the order of length being 4, 3, 2,
1; they are very short, about one third the length of the body ;
the first and second are conical, the third flatter, with a slight
ridge externally, and the fourth broad and flat with a distinct
crest. ‘The suckers are in four series throughout, small, sphe-
roidal, and not very oblique; the horny ring is smooth. The
hectocotylus is not developed. The umbrella is evanescent,
extending at most only up to the second row of suckers: the
buccal membrane has five points and is rounded dorsally ;
the spermatic cushion is but slightly developed. The outer
lip is thin and grooved longitudinally, the ¢nner thicker and
papillate.
The Tentacle is as long as the head and body; the stem
being slender and indistinctly three-sided. The club is very
slightly expanded ; a protective membrane, grooved obliquely
on the dorsal aspect, is situated on the outer margin, and
there is a web on the internal side. The suckers are in four
or five series, which are slightly larger towards the inner
margin; the horny ring presents a few acute teeth.
The Surface is smooth throughout.
The Colour is a dull reddish grey above, yellowish below.
The Shell is a very elongate oval in outline; the chitinous
margin is very narrow and extends only.slightly over the
dorsal surface, which is finely granular and marked by the
divisions between the loculi: the ventral surface is somewhat
elevated and marked by a distinct but not very deep median
groove; the last loculus extends over more than one third of
the shell and is bounded posteriorly by an almost semicircular
line; the strie are very close; the limbs of the inner cone
arise about midway along the shell, pass backwards as low,
narrow, smooth fillets, and unite behind without forming any
deep cavity; the posterior extremity is curved towards the
ventral aspect and ends in a narrow blunt cone, to the apex
of which is attached the straight dorsally directed spine.
Hab. Off the Ki Islands, south of New Guinea (Station
192), 140 fathoms. One specimen, ¢.
Sepia kobiensis, n. sp.
The Body is long and narrow, widest near the anterior
margin, and tapers gradually backwards. ‘he jin is very
narrow, only one eighth of the body; it commences 3 millim.
196 Mr. W. E. Hoyle on the
from the margin of the body and posteriorly passes on to the
ventral surface and terminates 2 millim. from its fellow and
A millim. from the extremity of the body. The manile-margin
has a narrow projection over the head, and is evenly truncated
ventrally. The siphon is short, not reaching halfway to the
space between the ventral arms.
The Head is of medium breadth, and the eyes prominent
laterally.
The Arms are subequal, the order of length being 2, 4, 3,
1, and less than one third of the length of the body; the first
two pairs are subconical and slender, the third broader and
with a web running up the ventral aspect, the fourth wider
and with a distinct ridge along the outer edge; they all taper
to very fine points. Many of the suckers are deficient, but
they seem to have stood in four series throughout; they are
spheroidal and very oblique ; the distal margin of many has a
deep notch: the horny ring is smooth in most cases, but
occasionally possesses afew angular teeth. The hectocotylus is
not developed. The umbrella is but little developed, its
greatest extent being on the ventro-lateral aspect, where it
reaches the fourth row of suckers. The duccal membrane has
the usual seven points, the two ventral being the least distinct
(as usual in female specimens); the spermatie cushion is
small. The outer lip is narrow, the inner wide and papillate.
The Tentacle is shorter than the body and slender; the
stem has three sides, the inner being slightly hollow, with a
slender fillet along the middle. The club is slightly expanded
with a distinct protective membrane; the inner side of the
club is deeply grooved, and internally to the groove is a rather
broad fin. The suckers are in about five series ; near the inner
margin are three rather larger than the rest, which gradually
diminish towards the outer margin. The horny rings of the
larger suckers have about twenty fine teeth on the distal
semicircumference, the smaller have fewer in proportion.
The Surface is smooth all over.
The Colour is a dark purplish grey above, paler below.
The Shell is avery elongated oval in outline; the chztinous
margin is very narrow and extends one third over the dorsal
surface, Which is smooth and evenly convex, with the excep-
tion of a slight ridge along the middle line: the ventral sur-
face is elevated, so that the shell is thick, with a shallow
median groove becoming evanescent posteriorly ; the Jdasé
loculus occupies one third of the surtace and is bounded by a
slightly curved line with a cusp where the median groove
meets it: the nner cone is formed by two limbs, which arise -
halfway along the shell and form rounded fillets shghtly
~~
‘Challenger’ Cephalopoda. 197
more elevated posteriorly, where they bound a shallow depres-
sion: outside them the margin of the shell expands into a sub-
circular plate, from the centre of which the spine projects
backwards; no information can be given as to its form or
length, as it has been broken off close to the base.
Hab. Kobi, Japan, 8 fathoms. One specimen, ?.
Sepia papuensis, n. sp.
The Body is elongated, broadest about one third back,
pointed behind: the jins extend the whole length of the body
and are one third of its breadth, a little wider behind; they
extend to within 1 millim. of the anterior margin, but are
separated by about 5 millim. posteriorly: the mantle-margin
projects far over the head dorsally, and is slightly emarginate
ventrally. ‘The siphon is conical, reaching two thirds up to
the gap between the ventral arms.
The Head is short and broad; the eyes prominent.
The Arms are subequal, their order of length being 4, 3,
1, 2; they are about one fourth as long as the body and taper
to fine points: the dorsal are conical with a very slight ridge
up the outer aspect, the third pair have a similar ridge; the
ventral are flattened and bear a distinct crest. The suckers
are in four series throughout and of moderate size, set ob-
liquely on short peduncles, with meridional grooves on the
outside: the horny ring bears from twenty to twenty-five long,
square-cut, irregular teeth in its distal semicircumference,
and outside it is an area covered with close-set papille. The
hectocotylus is not developed. ‘The wmbrellais slight, reaching
only as high as the sixth rew of suckers between the third and
fourth arms, where it is widest ; as usual it is entirely absent
between the two ventral arms. The buccal membrane has
the usual seven points. ‘The spermatic cushion is not deve-
loped: the outer ip is smooth, except for a few ridges due to
contraction ; the znner lip bears numerous small papille.
The Tentacles are about as long as the body, the stem being
three-sided : the c/ub is short, flattened, and expanded, with
a protective membrane on either side and a broad web down
the back, reaching along the stem for a distance equal to half
the length of the club; it bears six larger suckers in the
central row, a series of smaller ones on either side, and some very
minute ones along each margin ; at the top are from fifteen to
twenty in four series. The horny ring of the large suckers
has from twenty-five to thirty teeth in its distal semicircle ;
those of the smaller about ten.
The Surface is smooth, except for a few irregular incon-
198 Mr. W. E. Hoyle on the
stant papillz on one side of the ventral surface and below the
eye.
aot Colour is a pale yellowish grey, darker above.
The Shell is oval in outline, broadest anteriorly to the middle,
tapering somewhat rapidly in front and ending in a semi-
circle; posteriorly it tapers gently, and, then rounding off,
ends in two almost straight lines, which meet at a right angle
at the base of the spine. The chtténous margin extends but
slightly over the dorsal surface, which shows two grooves
diverging as they pass forwards, separating three ribs, and is
covered with rounded papille arranged in curves parallel to
the anterior margin. The ventral surface has a rather deep
and broad median groove: the /ast loculus occupies one third
of its extent, and is bounded posteriorly by a wavy line with
three parts; the striated area is hollowed, so that this part of
the shell is thin: the ¢nner cone commences by two limbs,
which arise halfway along the striated area, curve outwards,
and unite below the posterior apex with a broad chitinous
band passing from one side of the shell to the other and
forming a rather deep outer cone: the spine is short (but has
been broken off) ; it bends slightly upwards and has a narrow
longitudinal keel on its ventral surface.
Hab. South of Papua (Station 188), in 28 fathoms. ‘Two
specimens, ?.
Septa cultrata, Steenstrup MS.
The Body is elongated, broadest about the middle of its
length. The jins are rather narrow, about one fourth the
breadth of the body, commencing 2 millim. from the anterior
edge of the body and approaching within 5 millim. of each
other posteriorly ; the left is somewhat broader than the right.
The mantle-margin extends far over the head dorsally and is
not emarginate but slightly undulating ventrally. The szphon
is short, terminating far short of the depression between the
ventral arms.
The Head is broad, and the eyes very prominent.
The Arms are subequal, the order of length being 4, 3,
1, 2; they are one fourth the length of the body, all are
flattened and taper evenly to fine points. The suckers are
in four series, except in the right dorsal arm, where they
appear to be in two, probably owing to its state of extreme
compression; they are of medium size, many are deeply
notched proximally and distally, and provided with fine meri-
dional grooves on the margin: the horny ring is smooth and
surrounded by a papillary area. The hectocotylus is not
“Ohallenger’ Cephalopoda. 199
A PUaLop
developed. The umbredla is small, widest between the lateral
arms, where it reaches up tothe sixth or seventh row of suckers.
The buccal membrane has five distinct points, the ventral edge
being thickened and forming a large folded spermatic cushion ;
it bears no suckers. The outer lip is thick, and marked with
fine longitudinal grooves ; the ¢nner is papillate.
The Tentacles are as long as the mantle, with a three-sided
flattened stem, much broader proximally than distally. The
club is slightly expanded, with a narrow protective membrane
below, a broad one above, and a distinct web outwardly.
There are five or six series of suckers, slightly larger in the
middle than at the margins, on very long slender peduncles :
the horny ring is smooth.
The Surface bears a number of small irregularly scattered
papille, four or five elongated warts near the origin of the
fins on the dorsum, and some folds in the skin on the ventral
surface; probably these last are due to contraction.
The Colour is a dull grey, with a bluish shade above, inclin-
ing to yellow below.
The Shell has an elongate oval outline, broadest one third
of the way back and rounded off at both ends. The chztcénous
margin is narrow anteriorly, then broader, evanescent poste-
riorly, a deep calcareous ridge forming the posterior extremity
of the shell; it extends very little over the dorsal surface,
which bears only faint indications of a median ridge and is
beset with fine granules disposed in rows parallel to the anterior
margin. ‘The ventral surface is elevated so as to give the
shell a more than average thickness: the /ast loculus occupies
one third the surface and is bounded by a transverse hemi-
elliptical curve: the strzated area is excavated, but slightly
convex in the middle line. The nner cone consists only of
the slightly elevated limbs, which run along three quarters of
the striated area and unite with each other as a flattened fillet
posteriorly. The spzne has lost its extreme point, but is strong,
and has a raised knife-like ridge developed upon its ventral
aspect *.
id, Off south-east coast of Australia (Station 163), depth
2200 fathoms. One specimen, ¢.
METASEPIA, subgen. nov.
Sepia (Metasepia) Pfefferty, n. sp.
The Body is short and stout, broadest about the middle of
* Whence the specific name.
t+ Named after Dr. George Pfeffer of the Hamburg Museum.
200 Mr. W. E. Hoyle on the
its length, very thick (dorso-ventrally), and bluntly rounded
behind. ‘The fins are one fourth as broad as the body and placed
much nearer the dorsal than the ventral surface; they com-
mence 2-3 millim. from the anterior margin and are connected
by a narrow fillet behind; a slightly raised ridge passes down
the ventro-lateral aspect of the body, similar to that seen in
many specimens of Octopus and Hledone (possibly due to
contraction). The mantle-margin projects very slightly dor-
sally and is a trifle emarginate opposite the funnel: the con-
nective cartilages are deeper than in most species of Sepia,
but there is no distinct knob as in Sepiella. The siphon
reaches up to the depression between the ventral arms.
The Head is broad, and the eyes prominent.
The Arms are subequal, in order of length 3,4, 2, 1; they
are rather more than half as long as the body and distinctly
three-sided, having a ridge on the outer side of each, broadest
on the ventral ones; they taper evenly to very fine points ;
the inner surface of each is roughly papillate and has hemi-
spherical depressions into which the suckers are retracted.
The suckers are in four series throughout, almost hemisphe-
rical, not very oblique, and marked with meridional grooves:
the horny ring bears irregular square teeth. The hectocotylus
is not developed. The umbrella is larger than usual in the
genus, reaching on an average about one third up the arms;
the buccal membrane has seven not very prominent points, and
there is a spermatic cushion as usual: the outer lip is very
thin, the ¢nner thick and papillate.
The Tentacle is about as long as the body, stout, indistinctly
three-sided, and tapering. The club is short and but little
expanded, with a narrow protective membrane on its outer
side; the sucker-bearing area is, as it were, undermined on
its inner aspect by a deep groove or fissure, and internally
to this again is a broad fin which reaches down the tentacle
for a distance exceeding half the length of the club. There
are three suckers much longer than the rest, whereof the middle
one is the largest and the proximal the next, placed on stout
peduncles arising in deep depressions ; towards the outer side
of the club is a series of about four medium-sized suckers,
and beyond these again one or two series of minute ones.
The horny rings appear smooth under a powerful lens.
The Surface is smooth in general, but there are a few
‘irregular papille in the ventro-lateral region.
The Colour is a dull grey, with indications of annular
markings on the back.
The Shell has a rhomboidal outline, with rounded anterior
and lateral angles; the chitinows margin 1s narrow, widest
‘Challenger’ Cephalopoda. 201
behind, where it forms a flat, acute-angled plate, the posterior
extremity of the shell; it covers entirely, however, the dorsal
surface, which is slightly raised mesially and marked by a
number of faint striz radiating from the posterior end. The
ventral surface is much elevated on either side of a median
groove ; the Jast loculus occupies one sixth of the surface, is
bounded by a wavy line, and deeply emarginate in the middle.
The inner cone is represented only by a narrow rib reaching
halfway along each posterior side of the shell and meeting its
fellow in a rounded angle behind, from which a number of
radiating calcareous streaks pass outwards into the horny
termination.
Hab. South of Papua (Station 188), 28 fathoms. One
specimen, ?.
(gopside.
Histiopsis, Hoyle.
Eistiopsis, Hoyle, 1885, Narr, Chall. Exp. vol. i. p. 273 (nomen tan-
tum).
Resembles Calliteuthis, Verrill, in the shape of the body
and fin and in the pigment spots scattered over it, but has a
web extending for some distance between the dorsal, dorso-
lateral, and lateral arms: the suckers are in two series. The
siphon has a suspensory ligament anda valve. The gladius
has not been removed.
Histiopsis atlantica, Hoyle (loc. cit.).
The Body is short, conical; acuminate and curving gently
downwards posteriorly. The fin is about one third the length
of the body and considerably broader than long; each half
is roughly semicircular and narrows in to its insertion both in
front and behind. The mantle-margin is in general transverse,
but projects slightly as a blunt rounded angle in the dorsal
median line. ‘The mantle-connective consists of a groove with
a narrow median fillet in the mid-dorsal line fitting into a
corresponding cartilaginous surface on the back of the neck,
and of a long linear ridge extending up to the margin, which
fits into a shorter groove on the base of the s¢phon; this is
broad, short, and conical, and has a thick suspensory ligament,
through the skin of which two muscles may be distinguished,
and a distinct valve.
The Head is as large as the body, rounded at the sides and
flattened above and below. ‘The eyes appear to have been
enormous; one is distended and protrudes from its orbit, whilst
202 On the ‘Challenger’ Cephalopoda.
the other is shrivelled. There is no auricular crest and no
preocular pore, but behind each eye is a white papilla.
The Arms are about equal in length to the head and body
together ; the dorsal are the shortest, the other three pairs
subequal, the order of length being 3,4, 2,1; they are quadri-
lateral with rounded angles externally, with two slightly
raised ridges internally, on which the suckers are situated ;
they taper gradually to very slender tips ; the third pair have
a delicate narrow web along the third quarter of their outer
aspect. The suckers are in two series throughout; they are
small and distant along the proximal third (the webbed
portion) of the arms, then larger and closer, and finally minute
and very closely set towards the tips; they are set trans-
versely on short conical peduncles, spheroidal with a swollen
band round the face. The horny ring is smooth proximally ;
distally it bears about five close-set, broad, bluntly rounded
teeth. No trace of a hectocotylus could be found. ‘The wm-
brella is found only between the dorsal, dorso-lateral, and
lateral arms; it takes origin from the sucker-bearing ridge
and extends about one third up the arms. ‘The buccal mem-
brane is broad and somewhat contracted over the mouth ; it
has the usual seven points, but they are very blunt and indi-
stinct; it is united by three ligaments with the web between
the dorsal and dorso-lateral arms, by a ligament with the
inner side of each ventro-lateral arm on its ventral aspect and
by another to the inner surface of each ventral arm, there
being altogether seven ligaments. ‘The membrane bears no
suckers; its inner surface is much creased and folded. ‘The
outer lip is very thin and smooth, and hidden between the
creased integument of the buccal membrane and the inner lip,
which is thick and marked with irregular radial grooves.
The Tentacles have been removed ; the stumps which re-
main are not half the length of the arms ; they are quadran-
gular and flattened from above downwards.
The Surface bears a large number of papille, slightly ele-
vated, resembling those of Calliteuthis ; they are arranged
most thickly on the ventral aspect of the head and body, but
also on the dorsal, and extend up the outer aspect of the arms,
three series on the ventral arms, two on each of the others.
Near the tip of each dorsal arm is a series of four or five
black, elongate, egg-shaped swellings, gradually diminishing
in size, and forming apparently an extreme development of the
papilles above mentioned. The second pair of arms appears
to have been similarly provided ; the third has been so stripped
of integument towards the tips that it is impossible to ascer-
tain their original condition. In the fourth the warts at the
tip are quite similar to those lower down the arm,
On new Species of Histeridee. 203.
The Colour is a dull purplish madder, paler above than
below ; the papille are a deep black, with a white centre,
usually situated towards the anterior margin. The buccal
membrane, both sides of the umbrella, and the inner surfaces
of the arms, so far as this extends, are a deep purple.
The Gladius has not yet been extracted from the solitary
individual.
Hab. South Atlantic (Station 333), 2025 fathoms. One
specimen, sex ?
XXI.—New Species of Histeridee, with Synonymical Notes.
By Grorce LEWIS.
THE present paper is supplementary to one in this magazine
of last June, and treats of thirty-two species, twenty-four of
which are now described as new.
Two of the species are Onthophil’, making the total number
of described species in the genus nineteen ; and as there is no
reason for believing this genus to be less circumscribed in its
distribution than Platysoma or Paromalus, although its mem-
bers are much more difficult to capture, the genus will without
doubt ultimately prove to be a large one.
The genus Onthophilus is a very interesting one, as the chitin
of the exoskeleton is exceedingly opaque and evidently less
pure than in the other genera of Histeride ; and although some
of the species, such as sulcatus, are beautifully engraved above,
the substructure is, as it were, roughly hewn, and the meso-
and metasternal plates, as well as the abdominal segments, are
coarsely wrought at the sutures. When the chitin of Coleo-
ptera has the appearance of opacity and impurity, we often
see it accompanied with elaborate sculpture; and this is, in
fact, so general that it is impossible to avoid the conclusion
that the composition of the chitin is in some way the cause of
the coste and punctures which constitute the sculpture.
Sculpture and opaqueness are most obvious in those Curculio-
nide and Tenebrionide which inhabit sandy places or the
plains of extensive deserts; but they are by no means con-
fined to members of these families, for they exist in a marked
degree in many other insects which share their habitat.
Amongst the Histeride there is one very remarkable species,
Hister costatus, from Mexico, which has the opaque exoskele-
ton and the sculpture of Onthophilus, and it is the more worthy
of notice because three hundred species of the genus Hister
have purer chitin and a much less highly wrought sculpture.
. 204 Mr. G. Lewis on new
Lately I have had some analyses made in an endeavour to
discover what the elements are besides chitin in Brachycerus
and other desert species possessing a very opaque skeleton ;
but the results show that it is a line of investigation requiring
the life-labour of a first-class chemist rather than of a few
experiments conducted in the laboratory under the direction
of an entomologist.
List of Species, arranged generically,
Hololepta equa. Hister indicus.
prona. calidus, Hrichson.
—— maura. carnaticus.
—— Sahlbergi. —— martius.
—— Belti. —— Reaffrayi.
occidentalis.
limbatus, Truquz.
— complanata, Palis. Beauv.
Lioderma nudum.
Apobletes fictitius. Carcinops striatisternum.
planisternum, Levwzs. Triballus minimus, Ross?.
Platysoma cinnamomeum, White. tropicus.
—— punctulatum. montanus.
sexstriatum. Saprinus lautus, Wollaston.
exiguum. Onthophilus tuberculisternum.
Pachycrerus bellulus. bipartitus.
Raffrayi, Lewis. Idolia levigata.
Ebonius politus.
punctisternum.
‘Hololepta equa, n. sp.
Oblongo-ovata, plana, nigra, nitida; fronte equali; pronoto stria
marginali tenui pone oculos terminata, basi ante scutellum bisinu-
ato; elytris margine inflexo subtiliter rugoso, striis 3 dorsalibus
brevissimis prima appendiculata ; propygidio lateribus parce punc-
tato, apice bifoveolato; pygidio dense et grosse punctato. lL. 74
mill.
Hab. Assam.
H, equa is closely allied to endica; it differs in being nar-
rower and much smaller, and in having three elytral strie,
the first having a somewhat long appendicle.
Hololepta prona, u. sp.
Oblongo-ovata, subdepressa, nigra, nitida; fronte levi; pronoto
basi bisinuato, margine basi continuato, lateribus minime punc-
tato, stria interna ante basin evanescente ; elytris striis, prima in
medio late interrupta, secunda brevi subappendiculata ; prosterno
parce cincto-punctato, apice subbifoveolato; pygidio sat dense
punctato ; prosterno medio parum constricto. L. 94 mill.
Hab. Cape of Good Hope (ea coll. Monchicourt).
H. prona differs from maura as follows :—the margin of
the thorax is continued round the basal angle, the internal
Species of Histeride. 205
stria occupies two thirds of the length of the thorax only, and
the prosternum is anteriorly less wide.
Hololepta maura, n. sp.
Oblongo-ovata, subdepressa, nigra, nitida; fronte levi; pronoto
immarginato basi bisinuato, lateribus magis dense punctato, stria
basi continuata ; elytris striis, prima in medio interrupta, secunda. .
brevissima et appendiculata ; propygidio sparse cincto-punctato,
- apice bifoveolato ; pygidio sat dense subocellato-punctato; pro-
sterno medio sinuato; mesosterno antice marginato, subrecto.
L. 94 mill.
Hab. Abyssinia (Raffray).
This species is allied to the preceding, but the prosternum
is broader and less narrowed in the middle, the base being
half as wide again as the apex; in this respect it is like
lana. Also the thorax is more densely punctured at the
sides, the thoracic margin is absent, and the lateral stria
is carried round the basal angle, and anteriorly it terminates
in a shallow fovea. In maura and in prona there is a line,
not well defined, on the thorax in front of the scutellum.
Hololepta Sahibergi.
Oblonga, depressa, nigra, nitida; fronte punctulata, striis 2 trans-
versis brevibus ; pronoto lateribus sat dense punctato, stria mar-
ginali basi continuata ; elytris margine inflexo levi, striis 2 dor-
salibus, prima brevi, secunda integra; propygidio late circum-
punctato, medio linea haud distincta; pygidio parce punctato.
L. 7 mill.
Hab. Brazil (Dr. Sahlberg, no. 2794).
This species may be placed near cubensis and caracasia.
The second elytral stria is complete, as in lamina, but deviates
at both ends from the straight line; the propygidium is very
broadly punctured (not wholly so, as in caracasia), and the
pygidium is unevenly punctured, the punctures becoming
almost obsolete at the base. The elytral striz and facies are
similar to those of Lioderma rimosum and minutum, but the
wide prosternum brings Sahk/bergi into the genus Hololepta.
Hololepta Belti, n. sp.
Ovata, brevis, complanata, nigra, nitida; fronte plana, striis 2 trans-
yersis arcuatis subobsoletis ; pronoto lateribus anguste punctato,
ante scutellum bisinuato, stria marginali tenui; elytris margine
inflexo levi; stria subhumerali valida, basi abbreviata, 2 dorsalibus
obliquis, secunda brevissima, appendiculata ; propygidio punctis
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 15
206 Mr. G. Lewis on new
sparsis cincto, pygidio densissime punctulato; prosterno apice
sinuato, immarginato; mesosterno modice sinuato. L.7 mill.
Hab. Chontales (Belt).
This species is allied to curta, but is shorter: the chief
distinguishing characters are the absence of a long dorsal
stria, the fine and dense punctuation of the pygidium, and the
sinuosity in the apex of the mesosternum.
Hololepta complanata, Palis. Beauv. Ins. Afr. et Am.
p. 179, t. vi. fig. 5, appears to be closely allied to Lioderma
rimosum; but the description as under does not quite accord
with it in respect to the third stria, which is not visible in
rimosum :—‘Hister complanatus. Depressus, nigrescens, tho-
race levi, utrinque antice puncto impresso ; elytris abdomine
multo brevioribus ; striis 3, interiore brevissima; mandibulis
exsertis integris. Saint Dominique.
““Obs. Cette espéce, un peu plus petite que la précédente
[Lioderma 4-dentatum], se distingue par son corps presque
aussi plat que la Punaise des lits, et par la strie la plus in-
termédiaire qui ne se prolonge que vers le milieu de |’élytre.
De plus, le bas des élytres, dans |’Escarbot 4 Quatre Dents,
est tronqué de maniére 4 former I|’échancrure d’un cceur.
Enfin la couleur de |’Escarbot aplati est d’un noir brun et
non luisant.”’
Lioderma nudum, 0. sp.
Oblongo-ovatum, subdepressum, nigrum, nitidum; fronte impunctata,
striis 2 transyersis brevibus ; pronoto marginato, lateribus obsolete
punctato, stria interna basiabbreviata; elytris striis, prima integra,
secunda brevi appendiculata, tertia brevissima; propygidio punctis
parcis cincto, apice bifoveolato, pygidio dense punctato; prosterno
antice angustato, postice trigono; mesosterno antice marginato et
subsinuato. L. 9 mill.
Hab. Ashanti.
This species is doubtless very close to caffra, but the elytral
strie are different, and the thoracic punctures are nearly absent
and lie in asmall cluster near the middle of the margin. The
thorax is marginate; the lateral stria does not quite touch
the base, and in front terminates at the same point as the
margin behind the eye. The prosternum is narrow until it
widens out at the base in the form of a triangle; this last
character is also seen in caffra.
Apobletes fictitius, n. sp.
Oblongo-ovatus, complanatus, piceus, nitidus; fronte concava,
Species of Histeride. 207
stria recta supra oculos interrupta ; pronoto subtilissime punctu-
lato, margine tenuissime elevato, stria haud valida, pone oculos
evanescente, interstitio haud lato; elytris striis 1 et 2 validis,
integris, 3 in medio interrupta, 4 basali; propygidio transversim
grosse punctato; pygidio undique ocellato-punctato, margine
(basi excepta) elevato; prosterno levi; mesosterno transverso,
late sinuato, stria marginali integra. L. 5 mill.
Hab. Gilolo (Wallace).
A. fictitius is sculptured above almost exactly to the pattern
of Platysoma planisternum, but in the former the forehead is
concave. Beneath, the two species are also alike in the great
width of the mesosternum, but in jctitéus there is a well-marked
marginal stria, while in the other the surface is quite plain.
Platysoma planisternum, Lewis, should be placed in the
genus Apobletes.
Platysoma cinnamomeum, W hite.—The following is White’s
description of this species :—“‘ Smooth, deep rich purplish
brown; head in front considerably hollowed out; elytra near
the sides with three slightly curved, deeply impressed lines,
and three shallow impressed lines at the end of each elytron
between these and the suture. L. 13 lines.”
Hab. New Zealand (Capt. Parry).
Platysoma punctulatum, n. sp.
Oblongo-ovatum, subdepressum, nigrum, nitidum, supra punctulatum ;
fronte leviter concava, stria subrecta; pronoto stria laterali
integra, basi continuata; elytris striis 1-3 integris, 4 basi abbre-
viata, 5 dimidiata, 6 obsoleta; pygidio convexo ocellato-punctato ;
prosterno lobo marginato, punctulato ; mesosterno stria integra.
L. 5 mill.
Hab. Assam.
This species has the facies of many characters in common
with capense, which is very remarkable, because the localities
of these species lie 5500 miles apart. The abdomen beneath
is punctured alike in both species.
Platysoma sexstriatum, n. sp.
Oblongum, subparallelum, subconvexum, nigrum, nitidum; fronte
concava, stria integra supra oculos angulata ; pronoto stria laterali
integra; elytris striis dorsalibus 1-3 integris, 4 et 5 brevissimis ;
propygidio transversim punctato ; pygidio grosse punctato, margins
fortius elevato ; mesosterno sinuato et marginato. L. 5 mill.
Hab, Java (Raffray).
foe
208 Mr. G. Lewis on new
This species is very near to sériale and Robestorji, the
most conspicuous differential character being the strongly
elevated margin to the pygidium in the present species. The
dorsal striz are three in number, with slight indications of the
fourth and fifth at the extreme apex.
Platysoma exiquum, n. sp.
Oblongum, parallelum, subconvexum, ferrugineum, nitidissimum ;
fronte subconcava subtilissime punctulata, stria transversa recta
fortiter impressa; pronoto stria marginali integra pone oculos
angulata, lateribus subtilissime punctulato; elytris striis 1 et 3
integris, 2, 4, et 5 ante basin terminatis, suturali anterius abbre-
viata; propygidio grosse punctato ; pygidio levi, profunde bifo-
veolato (ut in P. 10-strzato); prosterno lobo parce punctato
marginato ; mesosterno stria integra late impressa ; tibiis anticis
acute 4-, posticis 3-denticulatis. L. 2} mill.
Hab. Dikoya, Ceylon. Discovered by my brother, A. R.
Lewis, in 1878 ; and a second specimen I found myself in
the spring of 1882.
The above is the smallest known Platysoma, and is allied
to 10-striatum, Motsch.; the mandibles in extguwm are very
fine and acute, with one large tooth in the middle.
Pachycrerus bellulus, n. sp.
Oblongus, cylindricus, viridi-cyaneus, nitidus, punctulatus; fronte
epistomoque marginatis, hoc impresso, stria transversa late inter-
rupta vel obsoleta; pronoto stria marginali antice interrupta ;
elytris striis 1-4 integris, 5 et 6 basi evanescentibus ; propygidio
pygidioque fortius punctatis ; prosterno stria marginali parallela,
mesosterno stria antice interrupta. L. 43 mill.
Hab. Abyssinia (Raffray).
This species in stature is intermediate between nigro-ceru-
leus and Raffrayi, and is closely allied to the latter. The
chief differences lie in the fourth and fifth elytral strie, in
the prosternal striz, and in the thoracic punctures; the last
in bellulus are finer.
Pachycrerus Raffrayt has the prosternal striez sinuate,
widening out in the middle; the thorax has a well-defined
fovea before the scutellum, and the epistoma is somewhat
excavated. In nigro-ceruleus the stria of the mesosternum
is well defined and the prosternal lateral striz are parallel,
as in bellulus.
Crypturus argtolus, Rossi, noticed in the ‘ Zoological
Species of Histeridee. 209
Record,’ 1883, as a Histerid, does not belong to the Coleo-
ptera.
EBONTIUS, n. gen.
Corpus subcylindricum, haud depressum. Caput retractile. An-
tenne sub frontis margine inserte, clava ovali 4-articulata, foveola
profunda sub angulo prothoracis. Pronotum antice angustatum.
Prosternum latum, marginatum. ‘Tuibie extus dentate. Propy-
gidium transyersum ; pygidium supra convexum apice reflexum.
This genus may be placed next to Omalodes, from which
it can be at once separated by the broad prosternum, the more
parallel form, and the singular pygidium, which is double, as
in Horn’s genus Teretriosoma.
Hbonius politus, n. sp.
Oblongus, subcylindricus, supra depressus, niger, nitidus; fronte
grosse punctata, margine plano antice interrupto; pronoto stria
integra, punctato, ante scutellum foveolato; elytris striis tenue
impressis, 1-3 suturalique integris, + et 5 punctiformibus, medio
abbreviatis ; propygidio utrinque punctato; pygidio medio sub-
tuberculato et grosse punctato. L. 83-9 mill.
Hab. Para.
_ There are two examples of this curious insect in the British
Museum, and I purpose shortly to give figures of both the
upper and under surfaces. The fore tibie have five or six
teeth ; the middle and hind pairs three each.
Hister indicus, n. sp.
Suborbicularis, convexus, niger, nitidus; fronte subtilissime et
parce punctulata, stria circulari; pronoto parce punctulato, stria
interna integra, valida, externa nulla; elytris striis crenatis,
subhumerali valida impressa, 1—4 integris, 5, basali rudimento
aucta, suturalique in medio, abbreviatis ; propygidio pygidioque
dense et grosse punctatis; prosterno basi lato et marginato ;
tibiis multispinosis. L. 43 mill.
Hab. Assam.
H. indicus is close to concordans, a species found in the
Deccan. The differences lie in the absence of the short internal
thoracic stria,the deep and complete subhumeral stria, the large
and deep punctuation of the pygidium, the widening out of the
base of the prosternum, and the lesser dilatation of the fore
tibie, which are armed with seven or eight spines in the place
of four teeth as in concordans.
Hister calidus, Er. J give the diagnosis of this species ; it
210 Mr. G. Lewis on new
appears to me to be identical with H. striolatus, but an exa-
mination of the type can alone decide this point :—“ Z. ovalis,
subdepressus, niger; thorace lateribus sesquistriato ; elytris
striis dorsalibus integris, laterali exteriore nulla; tibiis anticis
3-dentatis. Hab. Senegal. L. 4 lin. (Affinis H. mem-
mnonio.)””
Hister carnaticus, n. sp.
Ovalis, subconvexus, niger, nitidus; fronte subtilissime punctulata,
ineequaliter impressa, stria integra, modice valida, antice recta ;
pronoto antice bisinuato, stria laterali interna integra, externa
vix abbreviata; elytris striis 1-4 validis, integris, 5 brevissima,
suturali brevi media; propygidio punctis sparsis cincto; pygidio
levi; prosterno plano, emarginato ; mesosterno sinuato, stria
integra; tibiis anticis 3-dentatis, posticis biseriatim multispinosis.
L. 65 mill.
Hab, Nilghiri Hills.
This species belongs to an Indian group which embraces
corax and coracinus. H., carnaticus differs chiefly in having the
fourth dorsal stria deep and complete and the transverse band
of punctures on the base of the pygidium obsolete. The
group represented by encaustus and thibetanus has certain
characters in common with the above, and in a systematic
list the two clusters may be brought together with advantage.
ister martius, 0. sp.
Ovalis, parum convexus, niger, nitidus; antennis pedibusque rufis ;
fronte punctulata, stria profunde impressa; mandibulis extus
marginatis; pronoto basi punctato marginato, striis 2 lateralibus
integris profunde impressis ; elytris rubris macula communi angu-
lata nigra, striis validis 1-4 integris, 5 in medio subinterrupta,
suturali ultra medium abbreviata; propygidio pygidioque sat
dense ocellato-punctatis ; prosterno postice angusto marginato,
lobo punctato, in medio utrinque suleato ; mesosterno arcuato,
marginato ; tibiis anticis 4-dentatis, posticis biseriatim spinulosis.
L. 3 mill.
Hab. Abyssinia (Raffray).
This species is allied to /aco. It is slightly more convex,
the interstice between the thoracic margin and the outer stria
is much broader, the apex of the mesosternum is arcuate, and
the propygidium and the pygidium are densely marked with
ocellated punctures. The last character brings it near to
kurdistanus.
Mister Raffrayz, n. sp.
Ovalis, subeonvexus, nigro-piceus, nitidus ; fronte stria valida integra
Species of Histeride. 211
antice subrecta; pronoto marginato, stria laterali interna in-
tegra, externa subintegra, basi punctato ; elytris striis, subhume-
rali nulla, 14 integris, 5 in medio abbreviata, suturali arcuata
dimidiata; propygidio parce et grosse punctato; pygidio apice
levi; prosterno basi rotundato; mesosterno apice subsinuato,
stria integra, tibiis antice valide 3-dentatis, posticis spinulosis.
L. 4 mill.
Hab. Abyssinia (Raffray).
This insect may be placed next to martius. There is no
HMister at present in the list which has the fore tibie so
strongly denticulate, although in this characteristic castaneus
approaches it.
Hister occidentalis, n. sp.
Ovalis, convexus, niger, nitidus ; stria frontali semicirculari ; pronoto
stria laterali interna unica integra, margine punctato; elytris
striis 1-4 dorsalibus integris, 5, rudimento aucta, suturalique in
medio, abbreviatis; propygidio pygidioque sat dense equaliter
punctatis; prosterno margine striato; mesosterno subsinuato,
stria integra; tibiis anticis 7—8-denticulatis, posticis parce
spinosis. L. 5 mill.
Hab, China (? Shanghai).
This species connects the fauna of Asia with that of America,
as it is very closely allied to cognatus. It differs in the fifth
elytral stria being abbreviated in the middle and rudimentary
at the base, in the thoracic punctuation widening out into a
cluster behind the eyes, and in the propygidium and pygidium
being much less densely punctate. The specific name indicates
its locality from an American standpoint.
Hister limbatus, Truqui.—lI possess an entirely black ex-
ample of this somewhat rare species from Abyssinia,
Carcinops striatisternum, n. sp.
Oblongus, parallelus, parum convexus, niger, nitidus; fronte punc-
tulata, stria marginali integra, basi continuata, recta; pronoto
sparse punctulato, lateribus punctis grossis intermixtis, stria
integra ; elytris stria 1 integra, 2 postice punctiformi, 3 punc-
tiformi, 4 basi cum suturali juncta, 5 punctiformi basi inter-
rupta, subhumerali interna integra; propygidio pygidioque
punctatis; prosterno basi impresso, stria marginali basi termi-
nata; mesosterno sinuato marginatoque; metasterno utrinque
parallelo-striato. L. 135 mill.
Hab, Ceylon.
This species is more parallel than most in the list ; the meta-
sternum has on each side a very clearly defined stria between
212 Mr. G. Lewis on new
the middle and hind coxe and is thus divided longitudinally
into three parts. The external edge of the middle tibia is
armed in the centre with an isolated but fine and distinct
tooth. I took two examples in the touch-wood of an old tree
in the Dikoya district in the spring of 1882; they were
associated with a very pretty Megapenthes.
Triballus minimus, Rossi.—This common Huropean species
has a very wide range; I have a few specimens from Chefoo
and about thirty examples from El Hahaz, taken by Dr.
Millengen. All the Arabian examples are castaneous and
correspond to a variety standing in several cabinets under the
manuscript name of castaneus; but the Chinese specimens -
are typical.
Triballus tropicus, n. sp.
Ovalis, convexus, niger, nitidus, supra ocellato-punctatus et minute
punctulatus; antennis tarsisque rufis; fronte subconeayva sat
dense punctulata ad oculos elevata ; pronoto stria marginali antice
late interrupta ; elytris striis marginalibus mtegris ; propygidio
pygidioque sat dense punctulatis ; prosterno utrinque striato, stria
recta; mesosterno antice recto immarginato, margine laterali
arcuato. L. 2 mill.
Hab. Singapore.
This species is allied to kenigius, but it is much smaller,
and the prosternal lateral stria is straight. ‘The ocellated
punctures in tropicus are scattered amongst a rather fine
unctuation, the punctures disappearing gradually on the disk
of the thorax and on the dorsal region behind the scutellum.
The underside has an extremely fine rugosely punctate sur-
face, with a scattered punctuation of a larger grade, and this
punctuation is much larger on the first segment of the abdo-
men than on the metasternum. ‘The stria dividing the
mesosternum from the metasternum is crenellate, as in colom-
bius, kenigius, and others.
I found three or four examples in an old tree in the public
garden at Singapore, 11th February, 1880.
Triballus montanus, n. sp.
Orbicularis, subconvexus, rufo-brunneus, nitidus, undique grosse sat
dense punctatus ; antennis pedibusque rufis; fronte subconcava,
supra oculos valde elevata; pronoto stria laterali integra; elytris
striis dorsalibus punctiformibus, brevibus ; pygidio sparse punctu-
lato apice levi; meso- metasternoque ocellato-punctatis. LL.
2 mill.
Hab. Dikoya, Ceylon.
Species of Histeridee. 213
The colour of this species separates it from all the others
described. The punctures above are not distinctly ocellated,
but those on the under surface and on the broad abdominal
plate are clearly so. The elytra are clearly marginate, with
a lateral stria running parallel to the margin, which leaves a
fairly wide smooth interstice. The club of the antenna under
a high power is composed apparently of two joints, and the
ocellate punctures beneath are clearly seen under the micro-
scope. J’. americanus has a solid club.
I took about thirty specimens of this species from the
burrow of a longicorn larva on the 25th January, 1882, in a
large tree standing on Mr. Anderson’s estate.
Saprinus lautus, Wollaston, 1869, nec Hrichson, 1847=
bicolor, Fabr. Mr. Wollaston kindly sent me, in 1876, a type
of his species from the Congo River, and this enabled me to
decide the above synonymy ; but it is only just now published.
Onthophilus tuberculisternum, 0. sp.
Suborbicularis, supra gibbosus, niger, subopacus, griseo-setosus ;
antennis, scapo excepto, brunneis; pronoto 8-costato; elytris
sutura, margine laterali, costisque 3, elevatis, interstitiis foveo-
latis; propygidio pygidioque rugosis; prosterno concavo, basi
latiore, striis lateralibus integris; mesosterno medio tuberculato ;
metasterno medio longitudine suleato. L. 13 mill.
Hab. Zanzibar (Laffray).
The thorax of this species differs much from that of the next
in outline, as it is angulated as in alternatus. The sculpture
of the head and the pygidium is much obscured by the setose
growth upon them; the lateral stric of the prosternum in this
species and bipartitus are parallel to each other, and do not
join anteriorly as in 9-costatus. The mesosternum has a
well-defined somewhat linear tubercle in the centre, and the
metasternum is divided into two lobes by a line or sulcus
down the middle, and is sparingly punctured, each puncture
bearing a seta.
Onthophilus bipartitus, nu. sp.
Orbicularis, convexus, niger, subopacus, setosus; fronte rugosa,
margine elevata, medio subcarinata; pronoto parce punctato,
margine laterali fortiter elevato ; elytris sutura, margine laterali,
costisque 6, elevatis, interstitiis bilineatim punctatis; propy-
gidio pygidioque rugosis; prosterno subconcayo, stria laterali
integra; mesosterno transverso, angulis antice linea impressis ;
metasterno margine laterali elevato, cum sulco transverso impresso.
L, 13 mill.
Hab. Zanzibar (Raffray).
214 Mr. G. Lewis on new Species of Histeride.
This species is fashioned above like a small specimen of
9-costatus, but the mesosternum is without foveze and the
metasternum has a transverse semicircular furrow which divides
about one sixth of the surface from the posterior portion,
and the suture between the latter and the first segment of
the abdomen is indicated by a somewhat deep sulcus. The
margin of the prosternal lobe is narrowly testaceous.
IDOLIA, nov. gen.
Corpus perconvexum, fere orbiculare, nigro-piceum, nitidum. Caput
retractum ; fronte triangulari, margine elevato ; mandibulis
robustis. Antenne sub frontis margine inserts, fossa nulla,
scapo magno, funiculi articulo primo longiore, 3-8 squalibus,
clava abrupta ovali compressa 3- vel 4-articulata. Pronotum an-
tice angustatum, basi latum, stria marginali integra. Scutellum
triangulare. Elytris striis dorsalibus nullis. Prosternum latum,
lobo latissimo, marginato, basi truncato. Mesosternum antice
non sinuatum, a metasterno haud distinctum. Propygidium trans-
versum perpendiculare ; pygidium inferum obliquum. Pedes poste-
riores valde distantes ; tibiis minute denticulatis.
This genus has some of the characteristics of Spherico-
soma; it differs in having a large scape to the antenna and
in the great breadth of the lobe of the prosternum, which is
without fossettes and widens out to the lateral edges of the
thorax. Viewed from beneath the head cannot be seen when
in a state of repose, and the anterior structure then presents
the outline of a semicircle. Examined sideways there is seen
a deep cut in the anterior angle of the thorax between the
thoracic stria and the edge of the prosternal lobe for the recep-
tion of the antenna and part of the head, but this cavity cannot
be seen from above. ‘The antennz are drawn in with the
head, and during repose rest with it within the thorax. 'The
pygidium is beneath as in Notodoma, is semicircular at the
apex, and somewhat transverse at the base. The peculiar
structure of the thorax and the absence of true antennal
fossettes, and the construction of the meso- and metasterna
without apparent sutures, seem to indicate that the genus is
one of a low type, and it may be placed therefore after
Atletes.
Idolia levigata, n. sp.
Orbicularis, convexa, picea, nitida, pedibus antennisque dilutioribus ;
supra levis ; fronte subtilissime strigoso-rugosa, margine eleyato ;
pronoto stria marginali integra, basi arcuato, antice utrinque
obtuse angulato; elytris tenuissime marginatis: prosterno minute
Dr. Wallich on the Amcebe. 215
strigoso-rugoso lateraliter striato ; meso- metasternoque levibus.
L. 2 mill,
Hab. Honduras.
Distinguished from the following by characters given below;
it is hardly necessary to say the rugosity of the under surface
requires a microscope to discover it.
Idolia punctisternum, n. sp.
Orbicularis, convexa, brunneo-picea, nitida, undique sparse punctu-
lata; pedibus antennisque brunneis, his clava testacea; fronte
marginata; pronoto stria marginali integra, basi haud arcuato,
antice utrinque acute angulato; elytris tenuissime marginatis;
prosterno minute strigoso-rugoso, metasternoque sparse punc-
tulatis. L. 24 mill.
Hab. Blumenau, Brazil.
This species is exceedingly like the foregoing, but may
be at once recognized by the very distinct punctuation of
the under surface, the punctures being placed with singular
regularity at equal distances from each other. The base of the
thorax is much less arcuate in punctisternum than in levigata,
and the anterior angles in /evigata are, comparatively speak-
ing, obtuse.
XXII.— Critical Notes on Dr. Augustus Gruber’s “ Contribu-
tions to the Knowledge of the Amebe.” By Surgeon-
Major WaAtticH, M.D.
In the ‘ Annals’ for February 1882 there appeared a transla-
tion of a paper by Dr. Gruber bearing the above title*, in
which the author brought forward as new, and original on his
part, certain facts and observations relating to the organiza-
tion and vital phenomena in Ameba, which, as a matter of
fact, had been discovered and published by me, also in the
‘ Annals,’ upwards of twenty years ago. It so happened that
owing to long-continued serious illness I was prevented from
controverting Dr. Gruber’s statements at the period referred
to; and hence the matter became almost obliterated from my
memory. ‘To my surprise, however, the entire subject was
reopened by the appearance, in the ‘Journal of the Royal
Microscopical Society’ for April 1885, of a summarized ver-
sion of a further paper by Dr. Gruber, in which most of his
previously made statements were not only reiterated but con-
* Zeitschr. f. wiss. Zool, Band xxxi. pp. 459-470.
216 Dr. Wallich on the Amcebee.
siderably amplified on the very points which call for refu-
tation.
It may be within the recollection of some of the older
readers of the ‘ Annals,’ that in 1863 and 1864 a very detailed
series of six papers by me, on the Amceban, Actinophryan,
and Difflugian Rhizopods, was published in this Journal;
the first of the series, which appeared in April 1863, setting
forth the discovery, at Hampstead, of a till then unpublished
and publicly unknown form of Ameba, to which I gave the
name of A. villosa. ‘This Ameba presented some most re-
markable characters, and, being found in tolerable abundance,
I was enabled to study it very minutely, and thus bring to
light a large amount of information concerning the structural
and functional characters of the Rhizopods in general that
had not been previously available.
In the summary of Dr. Gruber’s second paper (published
<in the Journ. Roy. Micr. Soc. for April 1885, pp. 260-61),
A, villosa is referred to as “‘ Ameba villosa, Leidy.” ‘This
may, of course, be a mere clerical error on Dr. Gruber’s part ;
but, if not so, it becomes all the more inexplicable, as Dr.
Gruber, in his paper of 1882, makes such special reference to
Professor Leidy’s magnificent work on ‘The Freshwater
Rhizopods of North America’ as to indicate that he (Dr.
Gruber) was already critically acquainted with its contents.
As a matter of fact, Prof. Leidy distinctly and prominently
speaks of Ameba villosa as “a large and remarkable species
described by Dr. Wallich and discovered by him in England.”
Unfortunately, Dr. Gruber’s other inaccuracies of statement
in reference to the Amwbe do not admit of so ready expla-
nation ; for, apart from the obligation every writer on scientific
subjects is under of making himself acquainted with the dis-
coveries of those who have preceded him in any special line
of research, prior to sending forth any views of his own as
new and original, it is an unquestionable fact that a full list
of all my papers on the Amceban Rhizopods up to date,
together with extracts from the papers themselves on the very.
subjects so much more recently dealt with by Dr. Gruber,
was to be found in Prof. Leidy’s work. But, be that as it
may, I shall now proceed to place the facts of the case in a
sufficiently clear light to prove beyond question on which side
priority of observation as well as of publication rests. This
I will endeavour to do as briefly as I can compatibly with
due justice to Dr. Gruber as well as to myself. But, in a
matter of this kind, just conclusions can only be drawn from
the actually published records of both parties. I propose
therefore to supply, without comment of any sort, first, a
Dr. Wallich on the Amcebee. 217
few brief extracts from Prof. Leidy’s work already referred
to, and from a paper of Prof. Martin Duncan, showing how
far these two eminent authorities were acquainted with my
writings of 1863-64: secondly, to furnish such extracts from
Dr. Gruber’s two papers as may suffice to indicate clearly
those observations and statements of his that I desire to
criticize or controvert; thirdly, to furnish such extracts from my
own papers in the ‘ Annals,’ above referred to, as may be
needed to prove that my claim to priority is literally and
fully substantiated ; and, lastly, to conclude with some general
observations.
Pror. Lerpy.—‘ It appears from the researches, especially
of British authorities such as Carpenter, Williamson, Wallich,
Brady, Parker, and Jones, that the members of this class are
infinitely variable, and that, indeed, no absolute distinctions
of species and genera exist, such as appear more definitely to
characterize the higher forms of animal life. My own inves-
tigations rather confirm this view, and under the circum-
stances we can only regard the more conspicuous forms as so
many nominal species, in likeness with the species of higher
organic forms more or less intimately related, or by inter-
mediate forms or varieties merging into one another.’’
—Freshwater Rhizopods of North America (Washington,
1879), 0.1.6.
“ Dr. Wallich regards the endosare and ectosare as tem-
porarily distinct portions of the sarcode, mutually convertible
into one another. The ectosarc becomes differentiated from the
endosare by contact with the outside medium in which the animal
lives, and from time to time reverts again to the condition of the
more fluent endosare within. From this view, as intimated by
Dr. Wallich himself, the ectosare is due to a temporary and
partial coagulation of the endosare coming into contact with
the water in which the animal lives, and again reverts to the
condition of the more fluent endosarc as it retreats to the mass
of the latter within the body. This process reminds one of
the cooling of a molten mass of metal at the sides of a cru-
cible, and the melting away of the crust as it is stirred from
the sides of the molten mass within.” —Op. cit. p. 24.
“Dr. Wallich considers the so-called vacuoles or food-
vacuoles not in the light of mere spaces, but as temporary
vesicles of ectosarc, due to inversion of portions of the exterior
ectosarc at the time of the inception of the food, or to the con-
tact of water with poriions of the endosare.””—Jdid. p. 26.
“¢ While there is no absolute distinction between the ecto-
sare and endosare” (reference here made to A. Proteus),
“the two being continuations of the same protoplasmic mass,
218 Dr. Wallich on the Amcebee.
in the movements of the animal the endosare appears to flow
within walls, more or less thick, formed by the ectosare. With
the exhaustion of the endosare from behind, the including
ectosare contracts and melts away into the advancing portion
of the body.” —Op. cit. p. 38.
“Tn the taking of food he” (Dr. Wallich) “ supposes that
each portion when swallowed becomes enveloped with a film
of ectosarc, which forms a vesicle enclosing the food and
water-drop in the interior of the endosare. As the food under-
goes digestion, and the water, altered in condition, is imbibed
from the vacuoles into the contiguous endosare, the vesicles of
ectosare which contained the food and water undergo resolu-
tion into endosare.”"— Op. cit. pp. 43-4.
““ AMGBA VILLOSA. Ameba, Wallich, Ann. & Mag. Nat.
Hist. 1863, vol. xi. pl. viii. p. 287. Ameba villosa, Wallich,
ibid. p. 366, pl. ix. p. 434, pl. x. figs. 5-9. Duncan, Pop.
Sci. Rev. 1877, p. 217, pl. vi. figs. 38-40.
“6 Size, to sth of an inch (Wallich).
“« AMGEBA VILLOSA, a large and remarkable species, described
by Dr. Wallich, was discovered by him in England.”— Op.
cit. p. 63.
“’ Dr. Wallich’s remarks concerning the movements of
Ameba villosa apply equally to those of the form under con-
sideration’ (meaning Pelomyxa villosa, Leidy). “ He
says that ‘the rush of granules of the sarcode does
not follow upon a previous contractile effort exercised at the
posterior portion. As the animal progresses, occasionally
altering its course, there are periods during which perfect
quiescence is maintained by the granules; and the rush or
flow of these seems to take place, as it were, to fill up the
vacuum engendered by the sudden projection of a portion of
the ectosare.”—Ann. & Mag. Nat. Hist. 1863, xi. p. 369; op.
eit. p. Td.
iD, Wallich describes a conspicuous nucleus and an
equally conspicuous contractile vesicle as present in Am@eba
villosa, having the same essential characters and holding the
same habitual positions as in Ameba proteus. In the figures
accompanying Dr. Wallich’s memoir the single large nucleus
and the large contractile vesicle, or, in its place, several smaller
ones, are the most striking features of the creature.” — Op. cit.
. 80.
‘ Pror. Martin Duncan (“‘ Studies among the Amebe”’).
—‘ All that has been noticed in these studies will be found
somewhere or other, and I found it most interesting and in-
structive to study the work of Dr. Wallich in the Ann. &
Mag. Nat. Hist. for 1863. There the hairy Ameba is
Dr. Wallich on the Amcebze. 219
admirably described and christened Amba villosa, and all
its oddities are explained; there the reciprocal nature of the
endosare and diaphane”’ (a name given to the ectosare by
Carter), “the nature of the nucleus, and the method of its
subdivision, and, indeed, the exact morphology of the Amebe,
is given to perfection. ... One thing has struck me, and
that is that there are two species of Ameba only, and not a
score. There is A. villosa, which is a really crowned head ;
then there is the other, which, according to locality, time,
season, food, and the eyes of the observer, changes its general
shape and receives many names, and is called Ameba princeps.
It ought to be A. communis, as it is plebeian to the regal
villosa.””—Pop. Sci. Rev. 1877, p. 217.
Dr. GRuBER (‘‘ Contributions to the Knowledge of the
Amebe”’).— Auerbach, as is well known, starting from the
assumption that a membranous boundary was a necessary
attribute of a cell, set up a theory, quite compatible under the
circumstances of the time, according to which the Amebe
also, as unicellular creatures, had a membranous envelope.
This opinion was refuted by subsequent naturalists, and it
was Greeff principally who gave a more correct interpretation of
Auerbach’s observation.” —Translated version of Dr. Gruber’s
paper, Ann. & Mag. Nat. Hist. Feb. 1882, p. 106.
“The melting of the fine cortical layer into the broad clear
border does not take place with equal rapidity at all points, so
that a part of the Ameba often appears sharply limited, whilst
another is already surrounded by a clear space... . In this
way Ameba diffluens can continuously change its aspect
completely in one or other of the modes described. Upon what
law this power depends cannot be stated definitely; very
probably, however, different conditions of pressure come into
play in the matter. With acentripetal force acting uniformly
upon the whole periphery, the more fluid parts of the proto-
plasm are all pressed into the interior, and only the narrow
membranaceous boundary remains. This acquires a jirmer
consistence by contact with water, and therefore at the points
where the pseudopodia issue it is pushed aside by the latter.
If the general pressure ceases, the more fluid constituents
again come forth from the interior, dissolve the solidified cor-
tical layer, and form the clear border. The best illustration
of the process is furnished by those cases in which a slow
flowing forward of the Ameba in one direction is taking
place. On the advancing side the fluid constituents are pushed
on in front ; here all pressure has ceased, whilst it acts on the
opposite side, where, accordingly, the cortical contours are quite
distinctly to be seen.” —Ann. & Mag. Nat. Hist. Feb. 1882,
pp. 112-113.
220 Dr. Wallich on the Amceber.
“The pushing forward of the more fluid constituents is
effected by the action of a pressure on the opposite side; this
is produced by the extremest layer at this part acquirmg a
tougher consistency by extraction of water. The latter is
widened during the flow of the Ameba at the posterior end by
all sorts of processes, lobes, hairs, &c., which often give the
Ameba a peculiar aspect, and have led to the establishment of
distinct species. The sarcode here becomes so tough that as
the Ameba hastens forward it draws into threads, if the ex-
pression may be allowed. If the direction of movement is
reversed, the previous posterior extremity begins to flow, and
the most tenacious protoplasm occurs on the opposite side.” —
Ibid. p. 115.
“Gruber is of opinion that the discrimination of zones of
different kinds of protoplasm is due to a misunderstanding ;
the Ameebic body always consists of a single mass of proto-
plasm in which the various contents are suspended; when the
plasma is fluid the contents are well distributed, but when it is
firmer they do not mix so easily mith tt; this is the cause of
the appearance of a hyaline ectoplasm and a granular endo-
plasm. The only differentiation in the body of an Amoeba
obtains at the outermost periphery, where the protoplasm, clearly
from contact with water, ts converted into an invisible cuticula-
like layer, which disappears during the outpushing of the
pseudopodia, and can be remade.”—Hpiteme of Dr. Gruber’s
paper in the Journ. Roy. Micr. Soc. for April 1884 (p. 260),
the paper itself having been published in Zeitschr. f. wiss.
Zool. xli. 1884, pp. 186-225.
“The diagnosis of an Ameba must be based on its average
size, the consistency of the protoplasm, and the movements
therein conditioned, as well as on the characters of its contents,
such as vacuoles, granules, crystals, but chiefly on the number,
size, and structure of the nuclei. ive of the species described
in the present essay are multinuclear, and it is proved how
definitely the nuclei are distinguished from one another, and.
with what certainty one can conclude from external characters
on the structure of the nucleus, and vice verséd. ‘Thence results
the remarkable fact that two very similar species of Amaba
may have very differently formed nuclei, and that in forms
which are externally very different the nuclei may be quite
similar. In any case the number of the different forms of
nuclei is much more important than has hitherto been sup-
posed.” —Ibid. pp. 260-1.
The species lately described by Leidy and found by
Gruber in Europe confirm the doctrine that the freshwater
Rhizopods are cosmopolitan organisms.
Dr. Wallich on the Amcebe. 22%
My own Papers or 1863-4.—“‘ The Hampstead form”’
(Ameba villosa, so named in the paper succeeding that trom
which the present extract is taken) “corresponds in every
important particular with one found by me in Lower Bengal
in 1856, in which the villous portion of the ectosare consti-
tutes a means of permanent attachment to foreign bodies, such
as Confervee or the like; and the animal appears to be nor-
mally sessile in its habits.”—Ann. & Mag. Nat. Hist. April
1863, p. 290 *. .
‘When evaporation of the water” (in my aquarium) ‘ had
gone on to a greater extent, the entire granular mass referred
to became segregated, as if by a process of segmentation, into
numerous distinct nuclec, amongst which a true nucleus was
not recognizable as a separate or different structure. ‘These
multiple nuclei, varying in number from five to about a dozen,
were contained in no separate cavity or cavities, but occupied
the position previously occupied by the single large granular
mass. In the specimen exhibiting this structure the animal
seemed inclined to assume an encysted form, motion being
almost totally suspended.”—Ann. & Mag. Nat. Hist. May
1863, p. 368, pl. ix. fig. 5.
“¢ Another fact is deducible from the appearances presented.
by the sarcode-substance of the largest of these Amebe.
The rush of granules does not follow upon a previous con-
tractile effort exercised at the posterior portion. As the animal
progresses, occasionally altering its course, there are periods
during which perfect quiescence is maintained by the granules;
and the rush or flow of these seems to take place, as it were,
to fill up the vacuum engendered by the sudden projection of
a portion of the ectosarc in the shape of a pseudopodium.
Hence it would appear that motion is dependent on the con-
tractile power of the external sarcode-layer, and that the
endosare only passively participates in it. If this view is
correct, if involves a very important consideration ; for it
proves that the old German doctrine of a “ primary contractile
mucus’’ is essentially correct, and that the circulation is not
dependent, even in part, on the alternate expansion and
collapse of the contractile vesicle. Further than this, it
affords the strongest confirmation of the high degree of dif-
ferentiation existing between the endosarc and ectosare of the
Ameeban group.
“ The mysterious faculty resident in the latter portion of the
* No description of this Bengal Ameba had been published by me ;
but, as stated in a footnote to the above extract, in my ‘ North Atlantic
Sea-bed,’ published in 1860, pl. iv. figs. 13 and 14, a, 6, this remarkable
form is drawn in its occasional free and also in its sessile state,
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 16
222 Dr. Wallich on the Amcebee.
structure, of forming extempore orifices for the inception or
extrusion of food-particles, &c., may be witnessed in these
specimens in a very singular manner, and one which, as far
as I am aware, has not hitherto attracted attention. I allude
to the projection of the ectosarc from some area of the general
surface in the form of a hemispherical mass with a broad base,
only a very small portion of the original contour line seeming
to give way at first, so as to admit of the passage of the endo-
sare and other granular contents into the newly projected part,
but its entire floor appearing to be gradually dissolved, as it
were, and free communication between the main body and
the new pseudopodial cavity not being established until the
completion of this process. Whilst it is progressing, the
endosare-granules seem to rush round a corner into the cavity,
the corner gradually receding, so to speak, and ultimately
being altogether obliterated.
‘‘ Hyom these facts itis obvious that the ectosare and endo-
sare are not permanent portions of the Protean structure, but
mutually convertible one into the other ; and that it 1s an essen-
tial feature of sarcode that, whilst the outer layer for the time
being becomes, ipso facto, instantaneously differentiated into
ectosarc, the same layer reverts to the condition of endosare
under the circumstances just described. In the latter part of
the process, that is, the reversion to the condition of endosare,
the action is by no means so instantaneous as when the
converse takes place. In the Actinophryans both processes
are, comparatively speaking, slow.”—Ann. & Mag. Nat. Hist.
May 1863, pp. 369, 370.
“In iny experience the contractile vesicle does not make its
appearance either in the lowest order” (accordmg to my
classification), “‘ viz. the HERPNEMATA, or second order of Pro-
TODERMATA, but occurs for the first time in the third order,
viz. the PRoTeINA, in which I associate the Actinophryna,
Lagenide, and Amapina. In the third order both nucleus
and contractile vesicle are invariably present, though naturally
difficult of detection in the iestaceous genera. ‘The latter
organ, however, in so far as my experience of living repre-
sentatives of nearly every important form enables me to arrive
at a correct opinion on the subject, ought not to be regarded
as a definite-walled contractile sac, distinct in composition
from the rest of the protoplasmic matter, but simply as a
specialized vacuolar cavity, formed out of a portion of ectosarc.”
—Ann. & Mag. Nat. Hist. June 1863, p. 439.
‘In Ameba, the true ectosare appears to be nothing more
than the outer layer of sarcode (for the time being) consoli-
dated by contact with external influences, its thickness being
dependent on the length of time these influences continue
Dr. Wallich on the Amcebee. 223
without interruption to act upon it; whilst the consolidation
referred to is greater at the immediate surface, and gradually
diminishes in extent, and finally fades away from thence
inwards... Inthe nearly quiescent condition of Ameba,
when the outline becomes more or less spherical, the greater
amount of consolidation of the exterior layer is shown by the
hyaline margin becoming broader, and the whole of the contents
being, consequently, made to recede towards the centre... .
If not convertible into each other as I have described, how is
it that an Ameba may be lacerated so as to form two or more
portions, each of which immediately presents, at every portion
of its surface, the same appearance as existed prior to lacera-
tion, not necessarily by the folding together and union of the
torn margins, but by the immediate development of ectosare
upon the torn surface? Let the process be called instan-
taneous cicatrization, or what else we will, the phenomenon
remains the same.”—Ann. & Mag. Nat. Hist. Aug. 1863,
pp- 129, 130.
“The conversion of endosare into ectosarc, I regard as
analogous in its character, if not identical, with coagulation,
the effect produced by the mere contact of sarcode with the
medium in which it resides, while the converse process consti-
tutes an inherent vital function of the animal protoplasm.
Should this view be admissible, we have presented to us a
phenomenon bearing in the most important manner on the
general question of development, and one which, I venture to
affirm, is far more largely engaged in the production of specific
type, not only amongst the lower, but also the higher orders
of being, than we have heretofore been disposed to allow. I
allude to the reciprocal action of physical and vital forces.” —
Ann. & Mag, Nat. Hist. Aug. 1863, pp. 147, 148.
“TY am more than ever convinced that this” (the pseudo-
cyclosis in Ameba) “is not a vital act, but a secondary, and
merely a mechanical effect consequent on the inherent vital
contractility of sarcode. It is only necessary to watch a
specimen of Ameba carefully, to become convinced that the
appearance of a returning, as well as an advancing, stream of
granules ts illusory. ‘The stream, it will be observed, is in-
variably in the direction of the preponderating pseudopodial
projections. The particles simply flow along with the ad-
vancing rush of granules. There is no return stream, but the
semblance of one is engendered by one layer of particles remain-
ing at rest while another is flowing past them. In short, the
effect 1s similar to that which would be produced were a
transparent bladder or sac of caoutchouc, containing granular
bodies of greater specific gravity than the viscid fluid within
which they are suspended, to he rolled along a peue surface,
16
224 Dr. Wallich on the Ameebe.
In such a case it is obvious that only the granules on the upper
or free aspect of the sac would be carried onwards, that, having
arrived at the most advanced point, they would be, as vt were,
deposited, and remain stationary, as would also that portion of
the sac on which they rested, until the rest of the mass should
have again flowed over them, causing them now to appear at
the posterior extremity, when they would once more be urged on
as before.
“The same explanation will, I think, be found to hold
good in some families, as, for instance, the Foraminifera. ‘The
essential attributes of sarcode, extensibility and contractility,
coupled with the polymorphism evident on every example in
which definite form is not partially maintained by the presence
of a shell or test, necessarily involve the power of retracting
as well as projecting these processes, whereas the tenacity of
the substance is not such that a pseudopodium once projected
can be retracted towards the body in the same way that a
rope thrown forward from a given point can be hauled in
again, inch by inch. In the pseudopodium of Ameba, as also
in the attenuated filaments of the Foraminifera, or the still more
subtle filaments of Acanthometra or Huglypha, the process is
the same, and is brought about by the reciprocal outward and
inward flow of the sarcode substance ; and thus the granular
particles are merely the passive exponents of a vital force
which exists quite independently of them. Hence, with all
deference to such an authority as Prof. Schultze, I would still
regard the circulation of granules in the Rhizopods as a PSEU-
DOCYCLOSIS, analogous, I grant, in appearance but not in
origin to the cyclosis observable in certain vegetable cells, as,
for example, Tradescantia.’—Ann. & Mag. Nat. Hist. Nov.
1863, pp. 331, 332.
“ In the Amaban Rhizopods in general, without any excep-
tion, whether naked or testaceous, their protoplasmic substance
is differentiated into an anterior and posterior portion.” —
Ann. & Mag. Nat. Hist. Nov. 1863, p. 333.
“‘ Now contractility is the inherent property of protoplasm,
but not till it has become consolidated to a certain point ; and
this consolidation does not take place within the substance
itself, but only at the surface *. If we take the example of an
ordinary contractile substance the process is to al] intents the
same. ‘Thus caoutchouc, when oozing from the parent tree, is
not contractile but a semifluid viscid mass. So is the sarcode
* The formation within the general mass of the body-substance of
ectosare in the case of vacuolar cavities, or the contractile vesicle or vesi-
cles, as will be seen in a former extract, does not constitute an in-
trinsically originating process, but dependent, asin the true outer ectosarc
layer, on the presence of, or contact with water,
Dr. Wallich on the Amcebee. 225
in the interior of Ameba. But as soon as the action of the
atmosphere causes coagulation or consolidation of the tears of
caoutchouc, the innate contractility becomes at once manifest.
A precisely similar effect is produced by the contact between
endosarc and water. In the case of caoutchouc the consoli-
dation once established there is no return to the previous con-
dition. Why? Stmply because its vitality ceased with tts
extrusion from the tree. But even here the analogy is not
altogether destroyed ; for the contractility ” (elasticity) ‘‘ may
be materially diminished by heat, and the mass may again
become an adhesive semifluid, capable of permanently assuming
any figure. Yet, on the reduction of the temperature, consoli-
dation again takes place, and, with it, the mass resumes its
elasticity. So that, assuming sareode to be endowed with
vitality—a fact, I presume, not admitting of denial—and also
that it is contractile, we have not only all the conditions that
place the phenomena observed in the light of simple cause and
effect, but it appears to me absolutely impossible to ac-
count for them in any other way.’”—Ann. & Mag. Nat.
Hist. Dec. 1863, pp. 455-6.
General Remarks on the Foregoing Extracts—Concerning
Dr. Gruber’s “ Diagnosis in Amawba” *, I have to observe, that
in my experience the number of nuclei may vary almost to
any moderate extent, in certain forms and under certain con-
ditions. This fact becomes very obvious when the same
forms are observed, in the same localities, for several succes-
sive years. ‘To say that, because multiple nuclei occur in
forms which present no other—or, at all events, no other
important—characters which distinguish them from those pos-
sessing only single nuclei, they are therefore different species,
is scarcely a legitimate conclusion. or we find it very
commonly negatived im toto in the case of Amaba (as already
shown, anté), as well as in Arcella vulgaris and other forms.
When this Arced/a occurs in anything like abundance, and its
tests are neither too old nor too obscured by dirt, we may con-
stantly see several distinct nuclei within the body-substance
of the animal. In one example I observed no less than six.
The following memorandum in one of my note-books relates
to this specimen :— Oct. 21, 1864. Found a large Arcella
vulgaris, Dz45! with nine contractile vesicles, all peripheral
and acting energetically, but of course not synchronously.
Average interval between diastole and systole, as nearly as
I could estimate, about four minutes, ‘There were on this
specimen sia distinct nuclet of the ordinary size.”
Dr. Gruber’s Remarks as to PRESSURE being the Cause of
the Movement of Granular Particles de. in the Body-substunce
* See ante p. 220.
226 Dr. Wallich on the Amcebe.
of Amceba.—In one place, as will have been seen, Dr. Gruber
expresses himself somewhat doubtfully on this subject. He
says: “‘ Upon what law this power depends cannot be stated
definitely ; very probably, however, different conditions of
pressure come into play in the matter.” In a later part of his
remarks his doubts would seem to have already been resolved ;
for he there states unconditionally that ‘ the pushing forward
of the more fluid constituents is effected by the action of a pres-
sure on the opposite side,” &c. I confess my inability to under-
stand in what way “ different conditions of pressure” can be
developed, if such pressure be not an inherent vital attribute
of the sarcode-body itself, manifesting itself by the produc-
tion within its own substance of contractility and extensibility.
These effects are manifest in the Amebe in a very high
degree, and we know well enough that no pressure of any
ordinary kind could actually compress a fluid or semifluid
substance like sarcode, even in the slightest degree.
But, without any argument derivable from hydraulics or
hydrostatics, the vital, and, in this sense exceptional, cha-
racter of the force that causes a pseudopodium to be projected,
and, still more notably, a pseudopodium to be retracted, ap-
pears to me to be conclusively demonstrated by what happens
during the change from the extension of a pseudopodium in
one direction, to its retraction in the opposite direction. As-
suming that due precautions are observed to prevent illusory
effects, it will be seen that whereas the commencement of the
motion of the granules (which is the initiatory step in the
projection of a pseudopodium) is distinctly observable at the
most advanced portion of the mass which is going to constitute
such pseudopodium, the commencement of the retrograde
movement of the particles is to be seen taking place at that
portion of the pseudopodium which constitutes, not its apex,
but its base, each consecutive tier of granules pursuing the
same order until all are again reintroduced into the general
mass. In short, the order pursued by the granular units in
the projection and retraction of a pseudopodium is identical
with that pursued by a mass of human units when streaming
into an enclosed space through a single door, the human units
in front of the mass being naturally the first to flow in, even
when those in the rear have the civility not to exert pressure
on them; whereas in flowing out, the units who constituted
the rear would be the first to commence the retrograde move-
ment.
But to carry the case a point still further. Assuming, for
argument’s sake, that “ pressure”’ acts, as urged by Dr.
Gruber, by “extracting water” from a given portion of the
sarcode-body of Amwba, the explanation would in no wise
account for the collapse as well as the inflation with fluid of
Bibliographical Notices. 227
the contractile vesicle. If effective in forming, it could not by
any stretch of the imagination be truly regarded as the efficient
cause in the almost instantaneous reflux into the mass of the
body-substance of the ectosare constituting the contractile
vesicle. Besides, according to Dr. Gruber, the pressure he
refers to is exercised at the posterior aspect of the Amba,
and since the contractile vesicle almost always discharges
itself in that region, it would be doing so in the teeth of the
very force which is, at the very same time, exerting itself in
projecting pseudopodia in the opposite direction to the con-
tractile vesicle.
Having for the present brought these observations to a
close, it only remains for me to assure Dr. Gruber that I am
extremely glad to find that so able a writer and thinker has
been led, although by a different route, to conclusions concern-
ing the relations between endosare and ectosare, and the pheno-
menon of pseudocyclosis, similar to those arrived at by me so
many years previously.
BIBLIOGRAPHICAL NOTICES.
Australian Museum. Catalogue of the Australian Hydroid
Zoophytes. By W.M. Barz. Sydney: 1884.
Tue publication of the ‘Catalogue of the Australian Hydroid
Zoophytes, printed by order of the Trustees of the Australian
Museum, has supplied a want which has long been felt of a detailed
and critical account of the various species of Hydroids which have
been described from the Australian seas. Many of the older
species are known only by very brief descriptions, which, however
admirable at the time at which they were framed, have been
rendered, more especially in the absence of illustrative figures,
altogether indefinite, owing to the numerous allied forms which have
since come to light.
The present Catalogue contains, besides the description of a large
number of new or lately known forms, redescriptions or amended
descriptions of many of these older species in those cases where their
identification has been possible, while supplementary characters and
original remarks, often with considerable detail, on many of the
genera and species which are described give additional value to the.
work.
A special feature of the Catalogue is the large number of figures
which are given, and which, with but few exceptions, are from
original drawings.
It will thus be seen that the work is a valuable contribution to
the literature on zoophytology, and will form an important landmark
in the history of the Australian zoophytes.
228 Bibliographical Notices.
For the general student the usefulness of the Catalogue is greatly
increased by the succinct account, which is given at the beginning, of
the organization of the Hydroida, an account which, as is stated, is
mainly drawn from the Rev. Thomas Hincks’s ‘ History of the
British Hydroid Zoophytes,’ on the plan of which work the present —
Catalogue is largely modelled. Many interesting facts, based on the
author’s own observations, are incorporated with this portion of
the Catalogue, such, for example, as the occurrence in species of
Sertularia (S. crenata) of an intrathecal ridge, a structure chiefly
characteristic of the Aglaophenian section of the Plumularide ; and
the extreme variability in the nature and position of the external
apertures in the sarcothece of Aglaophenia.
Though the introduetory résumé of the chief features of hydroid
organization was by no means intended to be exhaustive, yet itis to be
regretted that no mention has been made by Mr. Bale of the neuro-
muscular or epidermo-muscular cells in the account of the structure
of Hydra on the one hand, or of the nervous system of the Medusa-
persons on the other.
As regards the distribution of the species, which have hitherto
been obtained almost entirely from the eastern part of the continent,
two distinct areas exist, one on the north-east, the other on the
south-east, in each of which the forms differ almost entirely from
each other, though mixing to some extent in the imtermediate
districts.
Thirty well-marked species occur only in the north-east region,
though four of these are found also in districts north of Australia ;
and eighty species are found only in the south-east region, many
of them ranging to Africa, Europe, and America, and occurring
more abundantly in New Zealand, with the Hydroid fauna of which
that of the south-east region is very closely allied. ‘Two species
only, Jdia pristis and Plumularia campanula, occur in both regions.
No genera are peculiar to the northern region ; but Linzolaria with
two species, Halicornopsis, Eucopella, and Ceratella with one each,
are found only in the southern district, together with that section
of Plumularia in which only one hydrotheca is borne on each piuna,
of which section one of the species, P. obliqua, occurs also in Eng-
land and Tasmania.
A list is given of the principal works in which Australian species
have been described, together with a more detailed list of the more
important general works on the Hydroida which are quoted or
alluded to in the text.
The systematic treatment of the genera and species forms the
greater bulk of the volume; and an idea may be formed of the
contribution which Mr. Bale has more directly made to the know-
ledge of the hydroid fauna of the Australian seas, when it is noted
that, out of about 125 well-defined species which are recorded, not
fewer than 47 have been made known by him.
Counting the undeterinined species of Hudendrium and Halecium,
144 species in all are described, of which about 16 are regarded as
doubtful. One species of the genus Hydra is recorded, for which
the order Eleutheroblastea, following the older classification, has
Bibliographical Notices. 229
been retained distinct from the Gymnoblastea. Seven species re-
presenting six genera, Tubularia with two species, and Tibiana,
Eudendrium, Pennaria, Ceratella, and Dehitella with one each,
belong to the Gymnoblastea ; while the other species, representing
seventeen genera, are forms of the Calyptoblastea, namely :—
Campanularia.. 12 species. Pasythea ...... 2 species.
belies 4...) .. Lee 3 TGR o.oo di ae
Eucopella...... ihe LLAUVEI UOT ai sse intel 3) aay
MGC OLON AE: sn Qa vr ys Plumularia .... 22 ,,
MOOD 3553. open lea Antennularia.... 2 4,
Halecum...... a enn Aglaophenia ..,. 22 ,,
Sertularia .... 40 ,, Halicornaria .... 10 ,,
Diphasia ...... De ae Halicornopsis.... 1 ,,
Sertularella .... 10
Among the new species which have been described in the Cata-
logue is one of the singular genus Lineolaria (consisting now of
two species), which was originally founded by the Rev. Thomas
Hincks for a most curious Australian hydroid from Port Phillip,
and for which Prof. Allman has since constituted a new family.
In the definition of the genus Sertularia Mr. Bale insists on the
paired condition of the hydrothece as being an essential character
which serves aS an important distinction between this genus and
its allies Sertularella and Thuiaria; and he points out that the
genus Desmoscyphus, Allman, is not really distinct from Sertularia.
A most remarkable variety of the Sertularia unguaculata, Busk,
which throws considerable light on the affinities of the genus, is
described, in which not only do some pinne bear as many as twenty-
four pairs of hydrothecee on the longest internodes, closely adnate
throughout the greater part of their length, while towards the end
of the pinne the ordinary Sertularian type is found, but also on
some of the pinne there is present a third series of hydrothece
running for some distance along the front of the first internode.
Very valuable critical remarks are made on the definition of the
genus T’hwaria. Formerly the adnate condition of the hydrothecss
was a sufficient distinction from Sertularia; but this has had to
be given up with the increase of our knowledge of their forms, and
the distinction was based by Prof. Allman on the nature of the
jointing of the hydrocaulus and the number of hydrothece on the
internode. Mr. Bale points out that this again must be abandoned,
and that the real distinction is to be found in the fact, that while
in Sertularia the hydrothecw are arranged in pairs, in Thuiaria they
form two series, those on opposite sides of the hydrocaulus having
no special relation to each other.
Correspondingly valuable remarks are made on various points
under the genera Plumularia, Aglaophenia, and Halicornaria ; but
it is to be regretted that the essential characteristics of Plumularia
and Antennularia have not been subjected to the same critical exa-
mination which marks many of the other genera.
In this short notice it has been impossible to do full justice to
Mr. Bale’s admirable work ; and the reader must be referred to the
work itself for further information.
230 Geological Society.
Elementary Text-Book of Entomology. By W. F. Kirsy.
London: Sonnenschein and Co., 1885.
Tue title of this book is somewhat misleading, which was probably
not the author’s fault, as his object was to furnish ‘“‘a portable
Hand-book, freely illustrated, in which a number of the most typical
and remarkable insects of all parts of the world should be popularly
described and figured.” To this end not less than eighty-seven plates
of woodcuts containing 650 figures, of which more than half are
devoted to Lepidoptera, are given. Woodcuts are not well adapted
for portraying insects; but, on the whole, the species are fairly
recognizable, a few, like Batocera rubus, Truxalis nasuta, Calepteryx
virgo, and two or three others, excepted. Most of the insects figured
are common in collections; and this is an advantage as enabling the
beginner to name his species, always a great desideratum.
Mr. Kirby has given short descriptions of most of the families,
and often of some of the species, as well as of their habits and
economy ; considering the necessarily limited character of the work,
this has been exceedingly well done.
As to the relationship of the Collembola and Thysanura, we should
prefer to follow Sir J. Lubbock, who has made them a special study,
and regard them not as “true insects” rather than as Neuroptera.
The Mallophaga also would be better placed with the Hemiptera, as
Gerstiicker, Claus, and others have placed them. But may we ask
why he has invariably commenced the specific names with a capital ?
It is, we think, very unfortunate that Mr. Kirby should have
reverted to the old name of Locustidz for the Gryllide, and that
he should have adopted Acheta for the classical Gryllus. The for-
mer name, a section of the genus Giryllus of Linnzus (by whom it
was first used, and not by Fabricius), should, by the law of priority,
revert to the mole-cricket (Gryllotalpa). It is perhaps quite as
unfortunate that he, in following the vicious practice of the Munich
Catalogue, which pays no attention to names previously used, pro-
vided that they are not used for Coleoptera, should have adopted the
generic name of the kangaroo for the harlequin beetle that forms
his frontispiece.
Mr. Kirby’s volume will be very useful to those who only require
a general idea of insect-forms; to the traveller, who cannot carry
many books with him, it will give a clue to the systematic position
of almost any insect he may acquire.
PROCEEDINGS OF LEARNED SOCIETIES.
GEOLOGICAL SOCIETY.
April 29, 1885.—Prof. T. G. Bonney, D.Sc., LL.D., F.R.S.,
President, in the Chair.
The following communication was read :—
“On the Structure of the Ambulacra of some Fossil Genera
and Species of Regular Echinoidea.” By Prof. P. Martin Duncan,
M.B. (Lond.), F.R.S., V.P. Linn. Soc., F.G.S.
After noticing the general knowledge which exists about the
Geological Society. 231
structure of the ambulacra in the Cidaride and the elaborate inves-
tigations of Lovén on the Triplechinide, the author brought before
the Society the results of his own work with and without the co-
operation of his fellow-worker in the description of the Hchinoidea
of Sind, Mr. Percy Sladen, F.G.S., and which referred to the Diade-
matide and the Arbaciade of the recent faunas. Starting with the
knowledge of the construction of the modern Diadematide, the
author investigated the genera Hemipedina, Pseudodiadema, Pedina,
Hemicidaris, Diplopodia, and Cyphosoma. The necessity for the
reestablishment of the genus Diplopodia was shown, and a new genus,
Plesiodiadema, was founded. Pseudodiadema, shorn of the forms
included in these genera, remains, and differs more from Diadema
than has been believed. The method of the growth of the great
plates of Hemicidaris was explained, and the comparison between the
peristomial plates of some of the Diadematide and the universal
structure of the ambulacral plates in Pedina was made. The author
considered that there are six types of ambulacra in the regular
Kchinoidea, so far as the group has been investigated, there still
remaining much to be done. These types are the Cidaroid, Diadema-
toid, Arbacioid, Echinoid, Cyphosomoid, and Diplopodous. In con-
clusion the succession in time of the structures which characterize
these types was considered.
May 13, 1885.—Prof. T. G. Bonney, D.Sc., LL.D., F.R.S.,
President, in the Chair.
The following communication was read :—
“On the Ostracoda of the Purbeck Formation; with Notes
on the Wealden Species.” By Prof. T. Rupert Jones, F.R.S.,
F.G.S8.
The author stated that in 1850 Prof. Edward Forbes had determined
the tripartite division of the Purbeck beds, after working at the sec-
tions in the south of England with Mr. Bristow, and had intimated
that several species of the so-called “ Cypridz ” aided him in arriving
at this result. Hedid not, however, publish any account of the several
forms, and we know of his intended species only (1) by his having
pointed them out to hisfriends Messrs. Bristow, Osmond Fisher, and W.
Cunnington ; (2) by a letter to Mr. Bristow in 1851 and one to
the Author in 1854; (8) by some diagrams in the Museum of
Practical Geology ; and (4) by some rough woodcuts in Sir Charles
Lyell’s ‘ Manual of Elementary Geology,’ 5th edit. (1855). Having
a large collection of Purbeck and Wealden Entomostraca, the author
has endeavoured to decide which were EK. Forbes’s species; and
from a careful examination of the collections in the Geological
Society’s Museum, the Museum of Practical Geology, and the
British Museum, in which he has been greatly assisted by Mr. E. T.
Newton, F.G.8., and Mr. C. D. Sherborn, he has arrived at the
definite conclusion that there are fourteen species in E. Forbes’s
three divisions of the Purbeck series. Five of them (Cypris pur-
beckensis, Candona bononiensis, C. ansata, Cythere Blake, and C.
232 Miscellaneous.
retirugata) occur only in the Lower Purbeck ; and of the others,
six occur in both the Middle and Upper. Of the fourteen, five
(Cypridea valdensis, very rare in the Purbeck, C. tuberculata, C.
Dunkert, Cyprione Bristovi, and Darwinula lequminella) go up
into the Wealden from the Middle and Upper divisions only. Cy-
pridea punctata for the Upper, C. granulosa ( fasciculata) for the
Middle, and Cypris purbeckensis for the Lower Purbeck, seem to be
always characteristic.
MISCELLANEOUS.
On a new State of Reticularian Rhizopods.
By M. ve Forty.
Amone the forms of Reticularian Rhizopoda belonging to the tribe
Nuda, that is to say those which live without envelopes, we have
distinguished some remarkable examples formed by a sort of mem-
branous sheath, developing in tubes filled with sarcode. These
tubes present numerous branches, the interlacings of which cross
one another upon several planes, giving to the whole the aspect of
an irregular network. hese form the genus Pseudarkys. We
find them sheltered in all the cavities presented by cld perforated
shells ; and from the mode in which they fill these and the multi-
plicity of branches of which they are composed, it might be sup-
posed that they had themselves hollowed out their shelters. Some
observations have shown us that this is not the case. One most
significant circumstance has just dissipated all doubts upon this
point, namely, the occurrence of aspecimen of Pseudarkys inhabiting
the cells of a Dentalina and adopting their form. It was very easily
distinguished through the semitransparent test, and in this position
it presented a clear proof that the organism certainly belonged to
the tribe Nuda. At its birth it had introduced itself into the
asylum, and in growing it had moulded its system of ramification
upon the inner walls.
The same animal, varying in dimensions according to the retreats
in which it had taken up its abode, was met with in a considerable
number of the dredgings of the ‘ Travailleur ;’ but the species seems
to remain the same. One of those of the ‘Talisman,’ on the other
hand, furnished us with an example of an alteration in the mode of
sheltering itself adopted by this organism. The branching, instead
of penetrating into a ready-made retreat, surrounded itself with
corpuscles, and especially with Globsgerine, which were very abun-
dant on the bottom on which it lived. In some cases, the envelope
not being completed, it was easy to see how its constituents were
united and cemented by the sarcodesma. In this new condition a
mass of sarcode was nearly always accumulated, forming, in all
probability, a sort of reserve destined to become converted into
Miscellaneous. 233
tubes, grafted upon those already in existence. This new mode of
living sheltered, differing essentially from the former, gave origin
to a new genus, Amphiewis, of the family Pseudarkysiz.
In a recent dredging at some distance from the southern shore
of the Bay of Biscay, upon a bottom of coarse sand, we found some
specimens of Amphiexis, that is to say organisms like those captured
by the ‘ Talisman,’ but differing from them in their envelope. The
enyelope, instead of consisting of Globigerine, is formed by an assem-
blage of sand-grains, of small shells of mollusca or their débris, and
a little mud. They also differ in having the sarcode which enve-
lopes the branched system much more condensed than in the specimens
from our shores.
The most interesting discovery that we have made is that of a
third state of the Pseudarkysiz. It is in the form of little pebbles,
and with the same hardness, that this organism presents itself. The
resemblance is so perfect that one is easily deceived. The organism
impregnates itself. with a paste which it forms with foreign cor-
puscles and sarcodesma, and thus forms a sort of cake, which it
“ices,” so to speak, by covering it with a composition of secretion
and sarcode, exactly analogous to that which forms the tests of the
porcellaneous Foraminifera. The covering is just as smooth, polished,
brilliant, and hard as the latter; but, instead of being white, it is
coloured in several shades. The sarcode which envelopes the
branched system is strongly condensed. If we break one of these
little false-pebbles the fracture is of the kind known as greasy.
This new state therefore gives occasion to the establishment of the
genus Lithozoa, and we believe that it may be divided into several
species.—Comptes Rendus, July 27, 1885, p. 327.
Description of a new Crustacean allied to Homarus and Nephrops.
By Srpyey I. Smira.
Any additions to the small number of known types of existing
Homaride are of special interest on account of the relations of the
group to the Astacide and to several fossil forms; and for this reason
it seems desirable to give a special notice of the following species
recently taken in the Caribbean Sea by the Fish-Commission steamer
‘ Albatross.’
KUNEPHROPS, gen. noy.
The species for which this generic name is proposed agrees with
Homarus and differs from Nephrops and Nephropsis in the number
and arrangement of the branchis, and in the evenly swollen branchial
regions; it agrees with Nephrops and Homarus and differs from
Nephropsis in possessing antennal scales and well-developed eyes ;
it agrees with Nephropsis and differs from Homarus and Nephrops
in haying very large antennal spines, and in being without any
spine on the second segment of the peduncle of the antenne; and
234 Miscellaneous.
it agrees with Nephrops and differs from Homarus and Nephropsis
in having slender and carinated chele.
Eunephrops Bairdi, sp. nov.
Female.—The carapax is nearly as broad as high, and the bran-
chial regions and the dorsum, except in front, are evenly convex
and rounded. The cervical suture is conspicuous and very deep,
extends round beneath the narrow lateral lobe of the gastric region,
and joins the middle of a conspicuous regularly semicircular suture,
limiting the hepatic region below and behind. The inferior edge
of the rostrum is sharp and slightly roughened, but not distinctly
dentate. From the sides of the rostrum two low rounded carinz
extend back a little way upon the gastric region, and are armed
each with two spines somewhat smaller than the lateral spines of
the rostrum, while much further back, upon the posterior margin of
the cervical suture, there is a pair of similar subdorsal spines much
nearer together. The anterior margin projects on either side in a great
vertically compressed dentiform spine, reaching in an acute point as
far forward as the eyes, and recalling similar spines in some of the
Crangonide. Just behind the base of the antennal spine there is a
small spine on the hepatic region, and between this and the poste-
rior subdorsal spine of the gastric region, and behind the orbit,
there is a similar spine. The carapax is everywhere roughened with
minute tubercles, between which the surface is beset with very short
hairs,
The eyes, though not quite so large, are nearly like those of
Nephrops norvegicus, being vertically compressed, reniform, and
black.
The antennule are like those of Nephrops norvegicus. The
general form and proportions of the bodies of the segments of the
peduncle of the antenne are almost exactly as in Nephrops norve-
gicus, but the second segment is evenly convex externally and with-
out any trace of a tooth or spine at the base of the very small
antennal scale, which is very little more than half as long as the
fourth segment, about half as wide as long, oblong-ovate, with a
minute tooth at the tip, and with the inner edge ciliated. The
flagellum is considerably longer than the body of the animal, and
very nearly as in Nephrops norvegicus.
The oral appendages agree very closely in every detail with those
of Nephrops norvegicus, except that there is a well-developed podo-
branchia, fully as large as in Homarus americanus, at the base of
the first enathopod.
In the single specimen seen the right cheliped is in process of
reproduction and very rudimentary. The left cheliped agrees in
general form very closely with the more slender of the chelipeds of
Nephrops norvegicus ; the inferior and superior edges of the merus,
though roughened with somewhat spiniform granules, bear only one
real spine each, and that at the distal end; the spines of the carpus
are slightly fewer, but arranged nearly as in Nephrops norvegicus ;
Miscellaneous. 235
the chela itself.is yery slightly broader than in Nephrops norvegicus,
the spines of the carine are a little less prominent, though the
caring are spinulose or minutely tuberculose nearly to the tips of
the digits, and the spaces between the carine are thickly tubercu-
lose, and not pubescent. The remaining pereopods are very nearly
as in Nephrops norvegicus.
The pleon is in general very much like that of Nephrops norve-
gicus, but the whole dorsum is pubescent, and the second, third, and
fourth somites have only an inconspicuous, transverse, dorsally
interrupted, and densely pubescent sulcus in place of the much
broader and conspicuous sulci upon all the somites of Nephrops nor-
vegicus. The depressions on the bases of the pleura are deeper than
in Nephrops norvegicus, and the inferior angles are more obtuse, and
not distinctly hooked, as in that species. The second to the fifth
pleopods are smaller and their lamellae much narrower than in the
Homarus americanus or the male of Nephrops norvegicus,
[I have had no female Mephrops for comparison. |
Measurements in millimetres.
Length from tip of rostrum to tip of telson..., 142-0
Length of carapax, including rostrum ......., 69°5
ene Of TOstruma yt Gy. 2 tlie cle wets ee ele eerie 24:3
Length of rostrum in front of spines.......... 13-0
Breadth between tips of antennal spines ...... 21°5
Greatest breadth, at branchial regions ......., 25:0
Height of carapax........-. Seo c HNO DAROn REELS 26:0
Length of eye-stalk and eye ........-++5.5:, 6:0
Greatest diameter of eye......0:..2s,e+002e> 70
Iength of antennal scale. .-.0-2.22055+++s+- 4:1
Breadth of antennal scale ..,.......2+.:0ee0s 2:0
Length of left cheliped ........... Sopkosbe8 1120
(ene thvotamenius ss 42 57,1..ctoetateatelobelais arin essoiels 32:0
lesa NIE COME se book be cn saCn SORA OD An en 22:0
Ligne AGE OIL She nceaoe sono nn nen OpOM Naor 54:0
BREACH CUCM EY sen.cenonconns HONDO NOUOO Re 12:5
Mierocavodachyiisi raat ne tere sles ia > 24:0
Length of second pereopod ...........0.00- 69:0
Weng thot menusy eects ante stlslale a dere see aris 23:0
DOME OORT bean oodnnag on neodnenon done 10°5
Geueth of chelay.- 5 .- 1 pas eri etic pe =o =e 18°5
Breadth: of ehielai cys tactrscycuiieystebeelet Nei curt -1a)p' el 3:0
Genet hot dachy lichen tens ti. tee G0)
Wencth of ‘third perscopodterm saith ame sar + 65:0
ILBNE TAGS Geo db oc bApodece condoeer oad 19°5
engi of carpus peer emia eres sates @ 96
Wengthvot Chelate meri secrete te > 20°5
Breadth of chelay ei Abeucttet stavetstet sisi tistt als 2°8
Weneth, of dactyluisy, cj agi euleiite ag ae ai fe ee 6:0
Length of fourth pereopod............200 58. 67:0
Meno th: Of propocuiss eager men Acts ella) i i-letcls 15°6
enoth of dacty Mister e emmittet tl. unite cai 9 8:7
Wensthok niphinencopodemanctac a= pals sere 58:0
Weneth of propoduss tte sss co nese es © 15:0
236 Miscellaneous.
Iength of dactylus: . 02..2°20). 2xc eciemlemnis = otal 7:0
Length of sixth somite of pleon.............. 13:0
Weength+of, telsoms:.fawyaqayctayhe orders -nek- ie eee 16:0
Breadth of telsony crc aa siesta sel ciete taken 13:3
Length of inner lamella of uropod .........+.. 140
Breadth of inner lamella of uropod .......... 13°3
Length of outer lamella of uropod............ 19-0
Breadth of outer lamella of uropod .......... 14-0
Station 2143, March 23, 1884; Gulf of Darien; north latitude
9° 30' 45”, west longitude 76° 25' 30"; 155 fathoms, green mud.
One female (6939).—Proc. United States Nat. Mus. 1885, p. 167.
New Haven, Conn., April 29, 1885.
On a Crocodiie-skull from the Tertiary Deposits of Eggenburg in .
Lower Austria. By Franz Touta and Jonann A. Kart.
The skull described by the authors was obtained from a sandy
deposit containing granite-blocks and rolled pebbles on the western
slope of the Calvarieaberg near Eggenburg. Remains of Halzthe-
rium were obtained from the same locality. The crocodile-skull was
in fragments, which, however, have been fitted together, and show
it to have been at least 73 centim. (about 30 inches) in length from
the imperfect muzzle to the hinder margin of the parietals, while
the greatest width is 35°5 centim. The bones of the roof of the
skull are pretty well preserved ; those of the under surface only in
the fore part.
From a comparison of the specimen with various recent and fossil
forms the authors conclude that it represents a new form inter-
mediate between Gavialis and Crocodilus. As regards the total
number of teeth (twenty) it would agree with the genus Tomistoma,
S. Mull. (= Rhynchosuchus, Huxl.), but it differs from this in haying
five teeth in the intermaxillaries (arranged as in Gavials), and in
having the sixth upper tooth the largest, instead of the fifth as in
Tomistoma. The teeth of the lower jaw fit into pits between those
of the upper jaw, the extremity of the snout is not enlarged, and
the suture of the intermaxillaries extends only to the third tooth of
the supramaxillaries— characters indicating relationship with V'om-
stoma, while the raised orbital margins remind one of Gavialis.
Mecistops has only seventeen teeth, and is further distinguished by
the enlargement of the snout at the end and in the region of the fifth
upper tooth ; while Gavialis has from twenty-seven to twenty-eight
teeth directed outwards, and differs in other characters. The authors
conclude that their specimen is to be regarded as a form inter-
mediate between Gavzalis and Crocodilus—most nearly related to the
genus Jomistoma, which -is now living in the rivers of Borneo and
North Australia—which they propose to name Crocodilus (Gavia-
losuchus, nu. gen.?) eggenburgensis.—Anzeiger d. k, Akad. d. Wiss.
in Wien, May 7, 1885, p. 107.
Cis PORN eae ea Po eee
CONTENTS OF NUMBER 93 a Series.
XVII. On Pheenicurus. By M. H. pu Lacaze-Dururers........ 157
- XVIII. On the Relationship of Ulodendron, Lindley and Hutton,
to Lepidodendron, Sternberg ; Bothrodendron, Lindley and Hutton ;
Sigillaria, Brongniart; and Rhytidodendron, Boulay. By Koxserr
ott Rees CR PALES OL ich Ws ecu unt chdohn a? neat Sukuietie ete a Me Rvan eee 162
XIX. Ona Variety of the Freshwater Sponge Meyenia Tes
auctt., trem Elorida. By EH. 3 Cantar, Wan Se G6. fish. Seas 179
XX, Diagnoses of new Species of Cephalopoda collected during the
Cruise of H.M.S. ‘ Challenger.’—Part Il. The Decapoda. By Wiru1am
E. Hoyrrtz, M.A. (Oxon), M.R.C:8., F.R.S.E., Naturalist to the
ratetisei a CHT OTSeIOR cS 2 laid ewes: Belen eine el era ais 181
XXI. New Species of Histeride, with Synonymical Notes. By
Grorce Lewis ..... Ree ROT aris tenance kent Supa wat ahaa oie tau Ronee 203
XXII. Critical Notes on Dr. Augustus Gruber’s “ Contributions
to the Knowledge of the Amebe. a By Surgeon-Major Watticu,
M. MN PC Ler cn ac Sea bite Ge A pia ose late De PMLNON a aha 215
=
BIBLIOGRAPHICAL NOTICES.
Eeatn Museum. Catalogue of the Australian Hydroid Zoophytes
pe METEIAR EE S57 feos ce ests airaivin sito auc sane taeda st 227
Elementary Text-Book of Entomology. By W. F. Kirpy ........ 230
PROCEEDINGS OF LEARNED SOCIETIES.
Geological Society :—Prof. P. Martin Duncan on the Structure of
the Ambulacra of some Fossil Genera and Species of Regular
Kehinoidea ; Prof. T. Rupert Jones onthe Ostracoda of the Pur-
beck Formation, with Notes on the Wealden Species .... 230, 231
MISCELLANEOUS.
On a new State of Reticularian Rhizopods. By M.pz Foun ...... 232
Description of a new Crustacean allied to Homarus and Nephrops.
» By Sopney I. Sure... . 20.5 Ber tas nets ae asaeinin Malar Widths ee 233
On a Crocodile-skull from the Tertiary Deposits of Eggenburg in
Lower Austria. By Franz Tovna and Jonann A. Kar ...... 236
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XXIII.— Descriptions of two new Species of Araneidea.
By the Rev. O. P. CamBripGE, M.A. &e.
[Plate IX. A. figs. 1 & 2]
Family Dictynide.
Genus DicryNna, Sund.
Dictyna cognata, sp. nov. (Pl. IX. A. fig. 1, a, d, c, d.)
Adult male, length 13 line.
In general appearance and size this spider nearly re-
sembles Dictyna arundinacea, Linn., to which it is closely
allied. It may, however, be easily distinguished by the spur
on the radial joint of the palpus. This spur is longer than
in D. arundinacea, its length beimg nearly equal to the
breadth of the base of the radial joint; it is also stouter, bent,
placed close to the base of that joint, and bifid at its extremity.
The radial is a little longer than the cubital joint, and its
spur is shorter than that of D. wneinata, 'Thor., from which it
also differs in the abdominal pattern. This pattern nearly
resembles that of D. arundinacea.
The spider from which the above notes have been made
was received from Holland, where it was found by Major-
General A. W. M. van Hasselt, who kindly submitted it to
my inspection, and has permitted me to describe it.
Family Theridiide.
Genus LITHYPHANTES.
Lithyphantes morsitans, sp. nov.
(PE TX Ae ties 25 a5.0,,C-)
Adult female, length 22 lines.
Cephalothorax short, broad behind, constricted laterally at
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. WY
238 On two new Species of Araneidea.
the caput; its colour is yellow-brown with a broad lateral
margin and the upper part of the caput of a deep brown.
The latter forms a longitudinal wedge-shaped band including
the eyes and continued backwards to the thoracic junction.
The eyes are pearly white, the four centrals form nearly a
square; those of each lateral pair are contiguous to each
other, and seated slightly obliquely on a small tubercle. The
height of the clypeus exceeds slightly half that of the facial
space.
The legs are slender, not very long, and furnished with
hairs and slender bristles. They are of a dark yellow-brown
hue; the femora have a single pale yellow-brown annulus
near their anterior extremity, and the tibie two pale annul;
the metatarsi and tarsi are paler than the other jomts. The
relative length of the legs is 1, 2, 4, 3.
Palpi short, slender, and of a dark yellow-brown colour,
furnished with hairs and a few bristles.
Falces not very long, rather weak, similar in colour to the
cephalothorax.
Maaxille, labium, and sternum normal, and of a deep brown
colour.
The abdomen isvery large and globular, and projects consider-
ably over the base of the cephalothorax. Its surtace is glossy,
of a black colour, sparingly furnished with hairs, and with a
rather sharply dentated, longitudinal, median band on the upper
side, continued in the form of a narrow simple band backwards
to the spinners. This band is of a dull pale hue, tolerably
distinctly edged with white; some two or three more or less
distinct oblique stripes of a similar nature occupy the sides ;
and on the underside, between the spinners and the genital
aperture, is a white spot or marking.
An example of this spider, alive, was kindly given to me
by the Rev. G. Aldridge, vicar of Morden, Dorset. It had
come to him by post in a small match-box from a friend in
Swaziland, Africa, where it is (probably not without reason)
considered venomous. I endeavoured to keep it alive, but it
refused to eat, and soon died.
EXPLANATION OF PLATE IX. A. figs, 1, 2.
Fig.1. Dictyna cognata, sp. n. a, abdomen, upperside, d; 6, genital
aperture, 2 ; ¢, palpus, ¢; d, portion of palpus, g, in another
position.
Fig. 2. Iithyphantes morsitans, sp. n. a, full figure, 2 ; 6, outline ditto,
in profile ; ¢, natural length of spider.
Mr. R. Kidston on Ulodendron, é&c. 239
XXIV.—On the Relationship of Ulodendron, Lindley and
Hutton, to Lepidodendron, Sternberg; Bothrodendron, Lindley
and Hutton; Sigillaria, Brongniart ; and Rhytidodendron,
Boulay. By Rosert Kipston, F.G.S8.
[Plates III.-VII.]
[Concluded from page 179. ]
It is necessary before leaving this portion of our subject
to make a few remarks on the Ulodendroid scars. It has
been stated by some authors that the large concave Ulo-
dendroid scars bore traces of leaf-scales; by others that these
were never present. It is, however, now unquestionable that
at one period of their development the whole area which now
forms the Ulodendroid scar was covered with leaf-scales.
This is clearly shown in Pl. IV. fig. 2 (specimen No. 3), and
in another and slightly older example (specimen No. 7). It
has also been stated, by those who believe that the surface of
the Ulodendroid scars originally bore leaf-scales, that these
were arranged in a system peculiar to the area of the scar.
At all events in the two examples just mentioned the leaf-
sears on the surface of the Ulodendroid scars are continuations
of the ordinary leaf-spirals of the stem. The presence, then,
of the leaf-scars on the Ulodendroid scar conclusively proves
that the appendicular organ, whatever its nature may have
been, cannot have been attached to the whole surface of the
scar, but only to its umbilicus. Further conclusive proof of
this is afforded by the Blackbraes specimen (No. 6) of Lepi-
dodendron Veltheimianum. (Pl. VI. fig. 11.)
The formation of the Ulodendroid scar may be thus briefly
described. In its earliest condition that has come under my
notice the area that supports the appendicular organ is slightly
elevated (Pl. IV. fig.2). The specimen (No. 7) which shows
the succeeding stage of development exhibits a clearly defined
semilunar outline, limiting the upper part of the scar, but no
boundary-line towards its lower part is yet visible. At this
stage of progression the leaf-scars are clearly seen on the
surface of the Ulodendroid scar, from the umbilicus down-
wards.
Fig. 9, Pl. V. (Stgillaria Taylor’), shows the attached
appendicular organs in a young state of growth. They are
directed upwards, and consequently the pressure exerted on
the bark by their leaves or bracts will be much greater on the
upper part of the Ulodendroid scar from the acute angle the
attached organ forms with the stem; and, in fact, it is on the
Lae
240 Mr. R. Kidston on the Relationship
upper part of the Ulodendroid scar that the leaf-scars are first
effaced. The continued pressure of the appendicular organ
against the cortex, augmented by the increase in girth of the
stem, causes the bark to swell up around its base, and thus
the characteristic Ulodendroid depressions are formed. On
the upper part of the Ulodendroid scar the leaves of the
attached organ first obliterate all traces of the leaf-scars, and
finally impress their own strap-shaped outline as radiating
lines from the umbilicus. On the lower part of the scar cir-
cumstances modify the case. The space here between the
attached organ and the bark is much greater than in the upper
portion of the scar; hence, though the attached organ eftaces
the leaf-scars on the stem by its leaves or bracts pressing on
its surface, they have not sufficient power to impress their out-
line on the Ulodendroid scar; thus the little “‘ dots,” which
mark the channels through which the foliar bundles have
passed are left to indicate the position of the stem-leaves. As
Schimper has pointed out, there cannot remain much doubt
that the appendicular organs result from a series of unequal
dichotomies, which were alternately fertile and barren, the
fertile probably forming deciduous cones, the barren carrying
on the axis of the plant.
Of actual cases where the appendicular organ has been
found zn sctu I only know of five:—-first, that mentioned by
Dr. Hooker* ; the second the notice given by Dr. Dawson, who
mentions having seen on one occasion the cones attached to
the stem +; the third the specimen figured by Mr. D’Arcy
Thompson }; the fourth and fifth those shown in figures 9 and
11 of this communication. That the appendicular organs were
aerial roots, as supposed by Mr. Carruthers§, has been pointed
out by Dr. Williamson|| and fully corroborated by the speci-
mens described in this paper.
* Mem. of the Geol. Survey of Great Britain, vol. ii. part 2, p. 427.
+ Acadian Geol. 2nd ed. p. 456 (1868).
t Trans. Edinb. Geol. Soc. vol. iii. pl. (B).
§ Notr.—tThe specimen on which Mr. Carruthers founded his belief
that the attached organs were aerial rootlets and directed downwards,
and which he figures on pl. xliii. fig. 5 of the Monthly Micr. Journ. for
March 1870, is in the collection of the British Museum (Natural History).
This specimen does not belong to Ulodendron, L. & H., but is a Halonian
branch of Lepidophioios. On the opposite side of the specimen to that
ficured there is a third row of tubercles; hence it cannot be a Uloden-
dron, L. & H. Again, the leaf-scars in Lepidophloios are directed down-
wards, and the view of those he gives in fig. 6 of the same plate proves
most conclusively that he has been dealing with Lepedophlovos, and not
Ulodendron. is fig. 5, then, is inverted ; so if his specimen were placed
in its true position; the tubercles would be directed upwards, which con-
forms with the ordinary Halonian branches of Lep:dophioios.
|| Phil. Trans. vol. clxxii. p. 209 (1872).
Aas
Se eter
of Ulodendron to Lepidodendron, de. 241
That the appendicular organs were caducous cones seems
most probable ; but I have not seen evidence sufficiently clear
to decide positively whether they were sessile or stalked. From
the evidence before us, however, and taking into account the
morphological significance of the attached organ, I have a
strong bias in favour of the opinion that the appendicular
organs were sessile cones. The view advocated by Stur that
they were bulbils does not appear to me to be at all probable,
and against it Schimper has stated sufficient objections*.
Before meeting with the specimens which form the subjects
of figures 2 and 9, it had often been a mystery to me why we
never found Ulodendroid scars on small stems, especially as
Halonian branches of Leptdophloios scoticus, Kidston, about
half an inch in diameter, are frequent. ‘This difficulty is
quite cleared up by an examination of the specimens nos. 3
and 18, of which the portion drawn in PI. IV. fig. 2, is
from a stem 44 inches broad (specimen No. 3), and that in
Pl. V. fig. 9 (specimen No. 18) from another over 3 inches
wide. It appears, then, that in the so-called Ulodendra it was
only the older stems that bore lateral cones.
It has already been pointed out that plants belonging to the
genus Lihytidodendron, Boulay, also possessed two opposite
rows of Ulodendroid scars}. It is true that Ulodendroid
specimens comparatively seldom show the leaf-scars well
preserved, and that on some of the described species of Ulo-
dendron they have not been observed ; still that does not alter
the fact that when well-preserved examples are examined
they show leaf-scars which conform to one or other of the
three genera Lepidodendron, Sigillaria, or Rhytidodendron,
as already mentioned. But if the form of the leaf-scar igs
of generic value in Lepidodendron, Sigillaria, and Rhytido-
dendron, on what grounds can we ignore the value of the same
character in Ulodendron? If, then, those plants with Ulo-
dendroid scars are to be excluded from Lepidodendron, Sigil-
laria, and Lhytidodendron, it will be necessary to form three
new genera for these plants—one for the Lepidodendroid UWlo-
dendra, another for the Sigillarian Ulodendra, and a third tor
the Rhytidodendroid Ulodendra. This view, however, I am
not prepared to adopt,.as I think the plants tind a suitable
and natural place in the genera Lepidodendron, Sigillaria,
and Rhytidodendron respectively.
Branching of Ulodendroid Stems.
The Sigillarian as well as the Lepidodendroid species of
* See ante, p. 135. tT See ante, p. 138.
242 Mr. R. Kidston on the Relationship
the so-called genus Ulodendron dichotomized in a similar
manner to that which occurs in Sigillaria and Lepidodendron.
In the former genus the dichotomizing of the stem appears to
have been much more feebly developed than in Lepidodendron,
and, in fact, there is strong evidence to show that some Szgil-
larie did not dichotomize at all*; but in regard to other
Sigillarie it is equally clear that they possessed a dichoto-
mized ramification t. Of Sigillaria Taylori, Carr. sp., several
dichotomizing examples have been found and described f.
The termination of these Ulodendroid stems has, however,
only been twice observed—first by Hugh Miller§, who
described it as having an ‘ abrupt cactus-like termination,”
and the other case is that figured in Pl. VI. fig. 10 (specimen
No. 17). This example is referable to Stgiilaria Taylori, to
which species Hugh Miller’s fossil most probably belonged.
I am not aware that any termination of a Ulodendroid branch
of Lepidodendron Veltheimianum has ever been discovered.
That they dichotomized in the ordinary manner has been
pointed out by Tate ||. Mr. Carruthers also gives a woodeut
of a specimen in a similar condition{j. J agree with Stur in
believing that Lepidodendron Veltheimianum, in addition to
bearing lateral cones (according to Stur lateral bulbils), also
bore terminal cones. Mr. C. W. Peach has shown mea large
slab, which I believe to be reterable to Lepidodendron Velt-
heimianum, on which are exhibited twenty-two cones attached
to small terminal twigs **.
Although our knowledge of the so-called Ulodendra has
been considerably augmented within the last few years, and
to such an extent that it appears to me impossible to regard
Ulodendron, Lindley and Hutton, as forming a true genus,
still there remain many points in regard to the structure of
these plants of which we at present possess only very imper-
fect information, and it is only by patient continued observa-
tion and collecting that we may ever hope to clear up those
points which are still mvolved in obscurity. I for one feel
very hopeful that many difficulties, not only in regard to the
Ulodendroid Lycopods, but in many other branches of fossil
botany, will yet be satisfactorily cleared up, only we must
* Goldenberg, ‘ Flora Sareepontana fossilis,’ Heft i. p. 25, pl. B. fig. 13
(Sig. reniformis).
+ Stur, Culm Flora, p. 296 (402), pl. xxv. (xlil.) (Srgellaria Eugenit).
t+ Thompson, /. ¢. p. 349; H, Miller, ‘Testimony of the Rocks,’ p. 464.
§ L.c. p. 464.
|| Tate, in Johnston’s Nat. Hist. of the Hastern Borders, p. 802 (1853).
4 Monthly Micr. Journ. vol. iii. p. 148 (1870).
** Collected at Grange Quarry, Burntisland, Fife, in Aug. 1876 (Calci-
ferous-Sandstone series).
of Ulodendron to Lepidodendron, dc. 243
wait till specimens are discovered which may fill in the
missing links, and not in the meantime supply what is at
present desiderated from the fertile regions of imagination
and desire.
IV. Synonymy AND NOTES ON THE THREE SPECIES
SPECIALLY CONSIDERED IN THIS COMMUNICATION.
LYCOPODIACEA.
LEPIDODENDRON, Sternberg, 1820.
[ Versuch eines geognostisch-botanischen Darstellung der Flora der Vor-
welt, 1. fase. 1. p. 25, fase. iv. p. x. |
Lepidodendron Veltheimianum, Sternberg.
(PI. III. fig. 1, Pl. IV. figs. 2, 3, 4, Pl. VL fig. 11.)
Lepidodendron Veltheimianum, Bronn, Index Paleont. p. 631; Dawson,
Foss. Plants of Lower Carb. and Millstone Grit, p.8; Etheridge,
Catalogue of Australian Fossils, p. 31: Grand’Eury, Flore carbon. du
Dép. de la Loire, p. 13838; Heer, Urwelt d. Schweiz, p. 7, fig. 2; id.
Foss. Flora d. Baren Insel, p. 38, pl. vii. figs. 1, 2 a-8, 3, 4, 5a, 6,
7, pl. ix. figs. 3, 4 (? fig. 2 a); id. Steink.-Flora d. arktischen Zone,
p- 4, pl. iv. and pl. v. fig. 3; id. Flora foss. Helv. Lief. i. p. 37, pl.
xvi. fig. 6 (P); Kidston, in Cadell, Trans. Ed, Geol. Soc. vol. iv.
p- 335; Konig, Icones fossilium sectiles, pl. xviii. fig. 236 ; Lesque-
reux, Coal Flora of Pennsylv. p. 374, pl. lxii. figs. 6-8 ; id. Geol. Surv.
of [llin. vol. ii. p.455; Renault, Cours d. botan. foss. p. 9, pl. v.
tigs. 1-2 (1882); Schimper, Traité d. paléont. végét. vol. ii. p. 29;
Schmalhausen, Mélanges Phys. et Chim. vol. x. p. 745, pl. i.
figs. 4-7; Sternberg, Vers. i. fasc. 4, p. xii, pl. li. fig. 3; Sterzel,
Bericht d. naturwis. Gesellsch. zu Chemnitz, vol. ix. p. 215 (1884) ;
Stur, Culm Flora, Hefti. p. 79, Heft ii. p. 375, pl. xviii. figs. 2-3,
pl. xix. figs. 5,6 (8?), 9, 10, pl. xx. figs. 1-6, pl. xxi., pl. xxii. fie. 3
(excl. figs. 1,2); Unger, Genera et Species, p. 256; Zeiller, Végét.
foss. du terr. houil. p. 110, pl. clxxii. figs. 3, 4.
Sagenaria Veltheemiana, Dawson, Quart. Journ. Geol. Soc. vol. xviii.
p- 299; Ebray, Végét. foss. d. terr. d. transition, p. 19, pl. v. (in
part), pls. vi., vii, and viii.; Hichwald, Lethza Rossica, vol. i.
. 119, pl. vil. figs. 2-6 ; Ettingshausen, Foss. Flora d. Mahr-schles.
Inches p- 106; Feistmantel, Zeitschr. d. deutsch. geol.
Gesellsch. vol. xxv. p. 528, pl. xvii. figs. 31, 32 ; Geinitz, Flora Hain.-
Kbersd. p. 51, pls. iv., v., vi. figs. 1-3; Giebel, Deutschl. Petrefacten,
p- 80; Goppert, Foss. Flora d. Uebergangsgebirges, p. 180, pls. xvii.—
XX., Xxiil. figs. 1-3, xxiv., and xliii. fig. 1; id. Neues Jahrb. p. 684
(1847) ; id. Flora d. Silur., Devon., u. unter. Kohl. p. 520, pls. xl.
fies. 3-4, xli. figs. 2, 4, xlil. fig. 1, and xliii.; id. Zeitschr. d. d. geol.
Gesellsch. vol. ii. p. 195; Romer, Palzeontographica, vol. iii. p. 46,
pl. vil. fig. 14 (1854) ; id. ibid. vol. v. p. 40, pl. viii. fies. 1-2 (figs. 4 &
5?) (1855) ; id. ibid. vol. ix. p. 10, pl. iii. fig. 6 (1862) ; id. Geol. v.
Oberschlesien, p. 55; Schimper, Végét. foss. du terr. de trans. d.
Vosges, p. 386, pls. xx., Xx1., xxil., and xxvi. fig. 6; Sternberg, Vers.
ii, p. 180, pl. lxviii. fig. 14.
244 “Mr. R. Kidston on the Relationship
° Stigmaria(?) Veltheimiana, Brongniart, Prodrome, p. 88; Unger,
Syn. plant. foss. p. 117.
Lepidodendron acuminatum, Stur, Culm Flora, Heft ii. p. 397,
pl. xxxix. fig. 4; Unger, Genera et Species, p. 261.
Sagenaria acuminata, Feistmantel, Zeitschr. d, d. geol. Gesellsch.
vol. xxv. p. 533; Goppert, Flora d. Silur., Devon., u. unt. Kohlenf.,
. 624; id. Zeitschr. d. d. geol. Gesellsch. vol. iii. p. 196; id. Foss.
lora d. Uebergangsgebirges, p. 185, pls. xxiii. fig. 4, xl. figs. 8-10;
id. Neues Jahrb. p. 684 (1847); Ludwig, Paleeontographica, vol. xvii.
p. 123, pl. xxvi. fig. 2; Romer, Geol. v. Oberschlesien, p.55; Schim-
per, Végét. du terr. trans. d. Vosges, p. 358, pl. xxvi. figs. 1-5.
Lepidodendron geniculatum, Schimper, Traité d. paléont. végét. vol. 11.
33.
Suen gentculata, Giebel, Deutschl. Petrefacten, p. 80; Goppert,
Foss. Flora d. Uebergangsgebirges, p. 186; Romer, Paleeontographica,
vol, iii. p. 46, pl. vii. fig. 18 (1854).
Lepidodendron patens, Schimper, Traité d. paléont. véeét. vol. ii. p. 36.
Selaginites patens, Brongniart, Prodrome, p. 84; id. Hist. d. végét. foss.
vol. ii. pl. xxvi. ; Bronn, Index paleont. p. 1132; Unger, Syn.
plant. foss. p. 141; id. Genera et Species, p. 272.
Lepidodendron glincanum, Schimper, Traité d. paléont. végét. vol. ii.
p- 84; Schmalhausen, Mém. Acad. Impér. d. Sc. d. St. Pétersbourg,
7¢ sér, vol. xxxi. p. 11, pl. 11. figs. 1 and 5-15, pl. i. figs. 1-14 (1883)
(excl. other figs. and syn. LZ. Volkmannianum).
Sagenaria glincana, Kichwald, Lethzea Rossica, vol.i. p. 127, pl. v.
figs. 21 & 22, pl. v.a, figs. 1-6 (? figs. 7-10).
Sagenaria confluens, Kichwald, Lethezea Rossica, vol. i. p. 121, pl. vii.
fie. 1 (excl. syns.).
Lepidodendron gracile, Romer, Paleontographica, vol. xiii. p. 218,
pl. xxxv. fig. 7.
Tepidodendron Jaschei, Romer, Paleontographica, vol. xiii. p. 218,
pl. xxxv. fig. 6; Schimper, Traité d. paléont. végét. vol. ii. p. 32.
Sagenaria polyphylla, Geinitz, Flora Hainichen-Ebersd. p. 53,
lL avale
Sanenanta aculeata, Feistmantel, Zeitschr. d.d. geol. Gesellsch. vol. xxv.
p. 531, pl. xvi. fig. 83; Goppert, Flora d. Silur., Devon., u. unt.
Kohl. p. 519, pls. xxxix., xl., xli.
Lepidodendron Sternberg, Heer, Foss. Flora Spitzbergens, p. 11,
pls. ni. figs. 1-20, iv. figs. 8 & 4 (excl. refs.).
Lan selaginoides, Heer, Foss. Flora Spitzbergens, p. 14,
1. iii. fig. 21.
Soba caudata, Geinitz, Flora Hainichen-Ebersd. p. 53, pl. iy.
fig. 4; Romer, Palzeontographica, vol. ix. p. 9, pl. iii. fig. 5.
Sagenaria elliptica, Goppert, Foss. Flora d. Uebergangsgebirges, p. 184,
pl. xiii. fig. 7; Ludwig, Paleontographica, vol. xvii. p. 122,
pl. xxvi. fig. 1, a, b, ¢, d.
Tycopodites dilatatus, Geinitz, Flora Hainichen-Ebersdo. p. 46, pl. x.
safer dle
Lepidodendron ornatissimum, Brongniart, Prodrome, p. 85; id. Hist. d.
végét. foss. vol. 11. pl. xvili.; Sternberg, Vers. i. fase. 4, p. xii.
Lepidodendron commutatum, Heer, Foss. Flora d. Baren Insel, p. 39,
pl. vil. figs. 8-10.
Bergeria regularis, Schmalhausen, Bull. de Acad. Impér. d. Se. d. St.
Pétersbourg, vol. xxii. p. 281, pl. ii. figs. 4 & 5.
Bergeria alternans, Schmalhausen, Bull. de l’Acad. Impér. d. Se. d. St.
Pétersbourg, vol. xxii. p. 281, pl. ii. fig. 6.
Knorria acicularis, Goppert, Foss. Flora d. Uebergangsgebirges, p. 200,
of Ulodendron to Lepidodendron, dc. 245
pl. xxx. fig. 3; Heer, Foss. Flora d. Baren Insel. p. 42, pl. viii.
fig. 2d, pl. x. figs. 6 & 7.
? Knorria anceps, Eichwald, Lethea Rossica, vol. i. p. 153, pl. xii.
fios. 2 & 3,
? Knorria mammillaris, Hichwald, Lethzea Rossica, vol. i. p. 155, pl. ix.
fig. 4.
Knorria imbricata, Geinitz, Flora Hain.-Ebersd. p. 57, pls. viil. fig. 3,
ix. figs. 1-8 (excl. figs. 2 and 4).
Fleningites pedroanus, Carruthers, Geol. Mag. vol. vi. p. 151, pl. v.
(1869).
Bee yas nucrodiscus, Eichwald, Lethza Rossica, vol. i. p. 106,
pl. v. figs. 2 & 3.
Ulodendron commutatum, Lesquereux, Coal-Flora of Pennsylv. p. 401,
pl. lxvi. fig. 2; Schmalhausen, Mém. de Acad. Impér. d. Se. d. St.
Pétersbourg, 7¢ sér. vol. xxxi. p. 17, pl. iv. figs. 7 & 8; Schimper,
Traité d. paléont. végét. vol. ii. p. 40, pl. ixiii.
Ulodendron parmatus, Carruthers, Monthly Microsc. Journ. vol. iii.
p. 152, pl. xliv. tig. 1.
Ulodendron Allani, Bronn, Index paleont. p. 1341; Buckland, Geol.
and Mineral. vol. ii. p. 92, pl. lvi. fig. 6.
Ulodendron ovale, Carruthers, Monthly Microsc. Journ. vol. iii. p. 152,
pl. xliv. fig. 1.
Ulodendron pumilum, Kichwald, Lethzea Rossica, vol. i. p. 144, pl. x.
fig. 5.
Tee Rhodeanum, Bronn, Index paleont. p. 1341; Unger, Syn.
plant. foss. p. 135.
Ulodendron Rhodi, Buckland, Geol. and Mineral. vol. ii. p. 93, pl. lvi.
fio. 6.
Ulodendron ellipticum, ? Bronn, Index paleont. p. 1341; Eichwald,
Lethza Rossica, vol. i. p. 140, pls. ix. figs. 6 & 7, x. figs. 3,4, & 6;
? Goldenberg, Flora Sareepontana fossilis, Heft i. p. 18; ? Sternberg,
Vers. ii. p. 186, pl. xlv. fig. 2; P Unger, Syn. plant. foss. p. 185;
Pid. (in part) Genera et Species, p. 264.
Ulodendron minus, Thompson (in part), “Notes on Ulodendron,” Trans.
Geol. Soc. Edinb. vol. i. p. 341, pl. a. figs, 2-3,
Ulodendron transversum, Wichwald, Lethza Rossica, vol. i. p. 189
(? pl. vi. fig. 13), pl. ix. fig. 8.
Ulodendron ornatissmum, Tate, in Johnston’s Nat. Hist. of the Eastern
Borders, vol. i. p. 802 (1853).
Phytolithus parmatus, Steinhauer (in part), Amer. Phil. Trans. vol. i.
2nd ser. p. 287, pl. vii. fig. 1 (1818).
Vegetable Impression, Allan, Trans. Roy. Soc. Edinb. vol. ix. p. 235,
pl. xiv. (1828).
“ Schuppenpflanzen,” Rhode, Beitr. z. Pflanzenk. d. Vorwelt, p. 16,
pl. i. figs. 1-8.
Remarks. Lepidodendron acuminatum appears to be only a
varietal form of Lepidodendron Veltheimianum, with which it
has already been united by Schimper.
Lepidodendron geniculatum is also merely a form of the
saine species. |
Lepidodendron patens (Selaginites patens, Brongn.), from
the neighbourhood of Edinburgh, is likewise to be re-
ferred to Lepidodendron Veltheimianum. The peculiarities
of Brongniart’s specimen arise from its mode of preservation,
246 Mr. R. Kidston on the Relationship
and many specimens from the Calciferous-Sandstone series,
from which horizon Brongniart’s example evidently origi-
nated, show the same characters. ‘The peculiar appearance
of the fossil to which the name of Selaginites patens has
been given is caused by the basal portions of the leaves still
retaining their attachment to the stem; and in other cases I
have observed a very similar appearance produced by the
leaves being adpressed (probably through mechanical agency)
to the branches. Although not for a moment doubting that
the specimens to which I refer are similar to that figured in
vol. ii. pl. xxvi. of the Hist. d. végét. foss., examples with
such an extremely scaly appearance are rare; but I have two
at least in which it is as well marked as in the type figure of
Lepidodendron patens, Brongn. sp.
Schmalhausen has united Lepidodendron glincanum, Hich-
wald, and Lepidodendron Volkmannianum, Sternberg, with
Lepidodendron Veltheimianum, Sternberg *.
With regard to Lepidodendron glincanum, I cannot find
any point by which it can be separated from Lepidodendron
Veltheimianum, and therefore include it under that name.
Lepidodendron Volkmannianum seems an altogether distinct
species, and cannot be united with Lepedodendron Veltheimi-
anum.
Lepidodendron (Sagenaria) glincanum, Eichwald, Lethea
Rossica, pl. v. a, fig. 7, should perhaps be referred to Lepr-
dodendron Volkmannianum.
Lepidodendron (Sagenaria) aculeatum, Feistmantel and
Goppert, Lepidodendron Sternbergii and Lepidodendron
selaginoides, Heer, and Lepidodendron (Sagenaria) caudatum,
Geinitz and Romer f, are all, I believe, referable to Lepido-
dendron Veltheimianum.
Lepidodendron Jascheti and Lepidodendron gracile, Romert,
are both young conditions of Lepidodendron Veltheimianum.
The transverse bars that occur on the leaf-scars of Lepido-
dendron gracile have most probably been produced by shrink-
age, and are frequently present on other species of Lepido-
dendron.
Bergeria regularis and Bergeria alternans, Schmalhauseny,
only appear to represent different conditions of preservation of
Lepidodendron Veltheimianum.
The core which lifted out of an impression of Lepedoden-
dron Veltheimianum in my own collection agrees so entirely
* Mém. de l’Acad. d. Sc. de St. Pétersbourg, 7° sér. vol. xxxi. no. 13,
p. ll. : ; 3
+ For figures specially referred to see synonyms given on pp. 245-245.
of Ulodendron to Lepidodendron, &c. 247
with Knorria acicularis that I have no hesitation in referring
that fossil to this species.
The explanation of how Knorria is formed will be learnt
from an examination of the internal structure of Lepidoden-
dron. As far as the present example of Knorria acicularis is
concerned, the more delicate tissue surrounding the central
vascular bundle appears to have decayed, and the bundle thus
freed has probably floated out of the cortical cylinder, which
subsequently became filled with sediment. Pressure now
acting on the cortical cylinder has forced the mud which filled
its interior up the small channels through which the foliar
vascular bundles passed to the leaves; the bark next appears
to have decayed, leaving the impression of its outer sur-
face on the surrounding matrix. The preservation of the
casts of the vascular-bundle channels has been assisted by
the decayed bark remaining around them in the form of a
fine powder, and so helping to prevent their obliteration by
subsequent pressure or infiltration. In this manner were
formed the little acicular points (the casts of the channels
through which the foliar vascular bundles passed) which
characterize Knorria acicularis, Géppert. Some specimens
of Knorria imbricata appear to be formed by a partial decay
of the outer surface of the bark before fossilization took
place.
It is impossible to correlate the various named species of
Knorria with the plants to which they really belong, as any
species of Lepidodendron might produce one or more
species of Knorria, according to the conditions which attended
its mineralization *. Lepidophloios and the Clathrarian
Sigillarie might also form Knorria-like fossils.
The type of Flemingites pedroanus, Carruthers, is in the
collection of the British Museum. I have failed to see any
character in which it differs from Lepidodendron Veltheimi-
anum.
The figure given by Mr. T. Allan of a vegetable impression
found in the quarry of Craigleith is a good example of Lepi-
dodendron Veltheimianum showing the Ulodendroid scars +.
This example was subsequently named Ulodendron Allani
by Buckland and Lepidodendron ornatissimum by Brong-
niart. Lindley and Hutton mention Allan’s figure as syno-
* There is in my collection a core, which lifts out of an impression of
typical Lepidodendron Velthermranum, and is identical with the figure of
Lepidodendron tetragonum as given by Geinitz in his ‘ Darstellung der
Flora des Hainichen-Ebersdorfer und des Flohaer Kohlenbassins,’ pl. iii.
fig. 2. My example came from the Calciferous-Sandstone series, Water
of Leith, between Slateford and Colinton, Midlothian.
+ Trans. Roy. Soc. Edinb. vol. ix. pl. xiv.
248 Mr. R. Kidston on the Relationship
nymous with their Ulodendron minus ; but this is a mistake,
for Allan’s specimen shows the Lepidodendroid leaf-scar,
whereas Lindley and Hutton’s plant belongs to the Sigillarian
section of Ulodendron. The plate of Ulodendron minus, L.
& H., would not at first lead one to this view; but from an
examination of the counterpart of their fossil, all that is
now preserved of their type*, I have been led to this con-
clusion. Ulodendron majus, L. & H., is only an older and
larger example of their Ulodendron minus ; hence its supposed
identity with Rhode’s pl. ii. fig. 1 is also erroneous. Lep?-
dodendron ornatissimum and Rhode’s pl. i. figs. 1-8 are
both referable to Lepidodendron Veltheimianum. Here must
likewise be placed Hichwald’s figures of Ulodendron ellipticum,
which all appear to represent more or less imperfectly-
preserved specimens of Lepidodendron Veltheimianum ; his
pl. x. fig. 6 +, in addition to exhibiting the leaf-scars of this
Lepidodendron, shows also on other parts of the same fossil
scars so preserved that they might be named with all pro-
priety “Anorrta.” It is questionable whether most of the other
figures which by different authors have been referred to Ulo-
dendron ellipticum really belong to this plant.
Ulodendron transversum, Hichwald +, pl. ix. fig. 8, is
another example, and a very interesting one, of the Uloden-
. droid condition of Lepidodendron Veltheimianum. In this
figure are seen the characteristic leaf-scars, a Knorria con-
dition, a decorticated state of the stem, and, finally, the large
Ulodendroid scar. Hichwald’s fig. 13, pl. vi., also probably
belongs to this species, but the actual proof that it does so is not
shown in the figure, which represents merely a Knorria con-
dition of Lepidodendron.
Similar remarks to those just made on Hichwald’s fig. 8,
pl. ix., may also be applied to his Ulodendron pumilum f,
pl. x. fig. 5. The large Ulodendroid scar appears to have
been partly covered by the matrix, and consequently looks
smaller than in some other examples, but does not seem to be
specifically distinct from them. It is identical with his Ulo-
dendron transversum, with which the leaf-scars agree in all
particulars. .
It is probable that the Ptychopteris microdiscus of the same
author is only a badly-preserved specimen of Lepidodendron
Veltheimianum. There is little evidence to support the view
that this fossil is a fern-stem.
* Jn the “ Hutton Collection,” Newcastle-on-Tyne.
+ For full reference see synonyms to Lep. Veltheimianrim, p. 245.
t This is not the same species as that subsequently named U. pumilum
by Mr. Carruthers.
of Ulodendron to Lepidodendron, cc. 249
Under Pachyphleus tetragonus, Gippert * appears to have
included portions of different plants. His fig. 5 cannot be
distinguished from a Ulodendroid scar of Lepedodendron Vel-
theimianum, but his other figures do not seem to belong to
_ this plant.
Some writers have proposed the union of Lepidodendron
corrugatum, Dawson, with Lepidodendron Veltheimianum; and
‘so closely does the last species resemble Lepidodendron
corrugatum, that Schimper and other paleeobotanists conver-
sant with the protean forms of this species, and knowing ours
only by imperfect figures, may well be excused for regarding
them as identical’? +. As mentioned in the above quotation,
some figures of Lepidodendron corrugatum are scarcely distin-
euishable from Lepidodendron Veltheimianum; but, through
the kindness of Sir Wm. Dawson, who has forwarded me a
series of specimens representing his plant at different stages -
of growth, I have been able to compare them with well-
preserved examples of Lepidodendron Veltheimianum, and
feel convinced that Lepidodendron Veltheimianum, Sternberg,
and Lepidodendron corrugatum, Dawson, cannot be united.
The three figures given by Stur in his ‘Culm Flora,’
pl. xxxix. figs. 1a, 1 6, and 2, do not belong to this species,
but to Sigillaria Taylorz, Carruthers, sp.
Localities and Horizons.
ScorLtanpD—Carboniferous-Limestone Series.
Ayrshire: Spittal Hill, Craigie Range, 34 miles S.E. of
Kilmarnock (Rev. D. Landsborough).
Lanarkshire: Shale above Calderwood Cement-stone, Kast
Kilbride (A. Patton); Possil Ironstone, Keppock
Hill, near Glasgow (J. Bennie) ; Carluke (collection
of British Museum).
Linlithgowshire: Roof of Easter Main Coal, Bo’ness (Z.
M. Cadell) ; Shale above Ironstone, No. 6 Pit,
Grange, Bo’ness (A. M. Cadell) ; Brown Ironstone,
Bo'ness (H. M. Cadell); Blaes, 20 feet above
Lower Ironstone, No. 6 Pit, Grange, Bo’ness (4.
M. Cadell).
Midlothian : Cowden, near Dalkeith (D. Grieve) ; Burgh-
lee Pitt, near Loanhead.
Stirlingshire: Todholes, Bannockburn, about 400 yards
above Bridge on Denny Road; Raploch Quarry,
near Stirling (G. Macdougall).
* Syst. fil. foss. p. 468, pl. xliii.
+ Dawson, Foss. Plants of Lower Carbon. and Millstone-Grit Forma-
tions of Canada, p. 21.
250 Mr. R. Kidston on the Relationship
ScortanD—Calciferous-Sandstone Series.
Berwickshire : Shore, Cove, Cockburnspath (J. Bennie) ;
Cliff, Cove, Cockburnspath (J. Bennie).
Fife: Kilmundy Limestone Quarry, Burntisland (J. Ben-
nie); Kilmundy Sandstone Quarry, Burntisland
(J. Bennie) ; Grange Quarry, Burntisland ; Dod-
head Quarry, | mile N.E. of Burntisland (J.
Bennie) ; Pettycur, Fife.
Haddingtonshire: Long-Craig Bay, 1$ mile west of
Dunbar.
Linlithgow: Shore, E. and W. of Society, Hopetoun;
Queensterry (J. Bennie); Shore, Dalmeny, EH. of
Newhall Pier (J. Bennie) ; Dalmeny (Dr. Macfar-
lane); Shore, near Long-Craig Pier, Dalmeny (/.
Bennie).
Midlothian: Raw Camps, near Midcalder ; Juniper Green
(7. Henderson) ; Shore, Wardie; Craigleith Quarry
(7. Allan); Addiewell, West Calder; Burdie-
house, near Edinburgh; Granton (J. Gaul) ; Water
of Leith, Spvlaw House, Colinton (J. Bennie) ;
Hailes Quarry, near Edinburgh ; Woodhall, Water
of Leith, near Juniper Green (J. Bennie) ; Straiton
Oil Works, near Loanhead; Shale over shell-bed,
Railway-cutting, 800 yards N. of canal, Murchiston,
Edinburgh (J. Bennie); Railway-cutting, Water
of Leith, between Slateford and Colinton (J. Bennie) ;
Straiton Brick-works, near Loanhead, West Calder.
EnetanD—From Rocks of Calciferous-Sandstone Age*.
Northumberland: Chirden Burn, near Hope House, North
Tynedale, specimen loose in drift (H. Miller) ;
Alnwick Moor (G. Tate); Yate Burn, 2 miles 8.8. W.
of High Long House; Chattlehope Burn, 2 miles
S.W. of Chattlehope House, Rede Water (7.
Fhodes) ; near Chillingham (Mus. N. H. Soc. of
Northumberland, Durham, and Newcastle-on-Tyne).
* The Calciferous Sandstones of the border counties are now looked
upon by the Geological Survey as being the equivalent of part of the
Carboniferous Limestone of Derbyshire and Yorkshire. The Scottish
“ Carboniferous-Limestone series” represents the Yoredale rocks of the
North of England.
England. Scotland.
Lower Carboniferous.
Moredmlemochseerrmcirat fms ae aauceemae Carboniferous-Limestone series.
‘bon i nes of Yorkshi 2 :
Carboniferous Limestones of Yorkshire | Galoifaroue-Sundetancicenee
and Derbyshire.
Devonian.
Devonian (Old Red Sandstone) ........ Old Red Sandstone.
of Ulodendron to Lepidodendron, dc. 251
SIGILLARIA, Brongniart, 1822.
[Sur la classification et la distribution des végétaux fossiles, p. 9.]
Section Olathrarie.
Stgillaria discophora, Kénig, sp.
(EEN jae soe PLN. tes 5) Ply VI ties 1251133)
Lepidodendron discophorum, Bronn, Index paleeont. p. 650; Konig.
Icones fossilium sectiles, pl. xvi. fig. 194 (1825).
Ulodendron majus, Bronn, Index palzont. p. 1341 ; Carruthers, Monthly
Micr. Journ. vol.iii. p. 153, pl. xlii. fig. 4 (1870) ; Giebel, Deutschl.
Petrefacten, p. 82; Goldenberg, Flora sareepontana fossilis, Heft i.
p- 18; Lesquereux, Geol. Survey of Ilin. vol. iv. p. 435; id. Geol.
of Pennsyly. vol. ii. p. 875; id. Coal Flora of Pennsylv. p. 401
(? pl. Ixvi. fig. 3) (excl. refer. Steinhauer) ; Lindley & Hutton, Foss.
Flora, vol. i. pl. v. (excl. refer.) ; Renault, Cours d. botan. foss.
p- 50, pl. xi. fig. 3 (1882); Rohl, Foss. Flora d. Stemk. Form.
Westph. p. 188; Schimper, Traité d. paléont. végét. vol. ii. p. 41
(syn. and refer. in part); Sternberg, Vers. ii. p. 185; Unger, Syn.
plant. foss. p. 134; id. Genera et Species, p. 263.
Ulodendron manus, Bronn, Index palzeont. p. 1341; Carruthers, Monthly
Mier. Journ. p. 225, pl. xxxi. (1869); id. ibid. vol. iti. p. 153
(1870) ; Eichwald, Urwelt Russlands, Hefti. p. 82; Giebel, Deutschl.
Petrefacten, p. 82 (excl. syn.); Goldenberg, Flora sarepontana
fossilis, Heft 1. p. 18; Lindley & Hutton, Foss. Flora, vol. 1. pl. iv.
(excl. refer.); Lesquereux, Coal Flora of Pennsylv. p. 403 (? pl. Ixvi.
fig. 1); Renault, Cours d. botan. foss. p. 50, pl. xi. fig. 2 (1882) ;
Rohl, Foss. Flora d. Steink. Form. Westph. p. 139 (excl. syn.) ;
Schimper, Traité d. paléont. végét. vol. ii. p. 42 (syn. in part);
Sternberg, Vers. ii. p. 185, pl. xlv. fig.5; Unger, Syn. plant. foss.
p- 185 (excl. refer. Allan & Brongt.) ; id. Genera et Species, p.. 263
(excl. refer, Allan & Brongt.); Zeiller, Végét. foss, du terr. houil.
. 115.
ede Mendon punctatum, Bronn, Index paleont. p. 173; Goldenberg,
Flora Sareepontana fossilis, Heft i. p. 18; Lindley & Hutton, Foss.
Flora, vol. ii. pls. Ixxx, & Ixxxi.; Morris, Trans. Geol. Soc. 2nd ser.
vol. y. p. 489; Renault, Cours d. botan. foss. p. 52, pl. xi. fig. 4
1882).
Ulodendron punctatum, Schimper, Traité d. paléont. végét. vol. ii,
. 42.
Bee aion Iindleyanum, Lesquereux, Geol. of Pennsylv. p. 875 (1858) ;
Sternberg, Vers. ii. p. 185, pl. xlv. fig. 4; Unger, Syn. plant. foss.
p. 135; id. Genera et Species, p. 263.
Ulodendron ellipticum, Rohl, Foss. Flora d. Steink. Form. Westph.
p- 189, pl. xxiii. fig. 3 (? fig. 4).
Ulodendron Stockesit, Buckland, Geol. & Mineral. vol. ii. p. 98, pl. lvi.
fig. 5; Carruthers, Monthly Micr. Journ. vol. iii. p. 152, pl. xliv.
fig. 3.
angi non Conybearv, Buckland, Geol. & Mineral. vol. ii. p. 94,
1. lvi. fig. 6’.
BERD On transversum, Carruthers, Monthly Micr. Journ. vol. iii.
p. 153, pl. xliv. fig. 2.
Ulodendron pumilum, Carruthers, Monthly _Micr. Journ. vol. iii.
p- 152, pl. xhii. fig. 2.
252 Mr. R. Kidston on the Relationship
DE ae Lucasii, Buckland, Geol. & Mineral. vol. ii. p. 93, pl. lvi.
Feel (ores parvus, Dawson, Acad. Geol. 2nd ed. p. 470, fig. 170g
(1868) ; id. Quart. Journ. Geol. Soe. vol. xxii. p. 163, pl. xi. fig. 50; id.
Canad. Natur. vol. viii. p. 453; id. Quart. Journ. Geol. Soc. vol. xxx.
p: ne ; id. Foss. Plants of Lower Carb. & Millstone Grit of Canada,
. 38.
Lenitsanons tetragonus, Dawson, Acad. Geol. 2nd ed. p. 490, fig. 170d
(1868); id. Quart. Journ. Geol. Soc. vol. xxii. p. 164, pl. x. fig. 49;
id. Canad. Natur. vol. viii. p. 453; id. Foss. Plants of Lower Carb.
& Millstone Grit of Canada, p. 37.
Lepidodendron salebrosum, Wood, Trans. Amer. Phil. Soc. vol. xiii.
p. 345, pl. viii. fig. 6.
Halonia disticha, Morris, Trans. Geol. Soc. 2nd ser. vol. vy. p. 489,
pl. xxxviii. fig. 1.
Stgillaria Preuiana, Romer, Paleeontographica, vol. ix. p. 42, pl. xii.
fic. 7 (1862).
Stgillaria perplexa, Wood, Trans. Amer. Phil. Soe. vol. xiii. p. 345,
pl. vil. fig. 7
Sigillaria Menardi, Lesquereux, Geol. Survey of Ilin. vol. ii. p. 450,
pl. xliii.
Description. Leaf-scars rhomboidal, contiguous, their trans-
verse diameter slightly greater than their vertical diameter,
placed on slightly elevated cushions, whose size but little ex-
ceeds that of the leaf-scar. Upper and lower angles of leaf-
scar rounded, lateral angles sharp and prominent. Vascular
impressions situated towards the upper part of the leaf-scar ;
central punctiform, the two lateral lunate. Certain branches
bear two opposite vertical rows of large (Ulodendroid) scars,
those of one row alternating in position with those of the
corresponding vertical row. Large scars more or less oval,
usually touching each other. Bark generally fissured longi-
tudinally, especially in older examples. Decorticated branches
also exhibit longitudinal fissures and show on their surface
small “ dots’ arranged in quincuncial order. Leaves single-
nerved, grass-like. J ructification (sessile ?) cones attached
to the vertical rows of large scars.
Remarks. I have found associated with this species peculiar
(sessile ?) cones (at least I have never seen them attached to
stems or twigs), which I believe to be the fructification of
this species. They appear to differ from the cones of Lepido-
dendron, and are the same as those figured by Brongniart
(Hist. d. végét. foss. vol. ii. pl. xxii. figs. 2, 3, and 8*).
As far as known to me, the ramification of this species has
not been observed, nor yet the termination of the branches.
This species was first figured as a Lepidodendron, without
any description, by Kénig, about 1825. Bronn is the only
* On the fructification of Sigzllaria, see Zeiller, Ann, des Sci. nat.
6¢ sér. Bot. vol. xix. p. 256.
of Ulodendron to Lepidodendron, cc. 253
author, as far as I am aware, who takes any notice of Kénig’s
plate, which is very characteristic of the species. A plaster
east of the specimen he figured is preserved in the collec-
tion of the British Museum; it measures 64 inches long and
3 inches wide, and bears two perfect Ulodendroid scars and a
portion of a third one. These are about two inches in dia-
meter. The rhomboidal leaf-scars are seen in the figure,
and a separate drawing of them is also given, but they show
no trace of the vascular-bundle “ dots.”
This, like all Kénig’s figures, is extremely characteristic
of the species, and is one of the best representations of the
plant with which I am acquainted.
Lindley and Hutton’s Ulodendron majus agrees in all re-
spects with this figure, which evidently must have been
unknown to the authors of the ‘ Fossil Flora,’ as they make
no reference to it. In regard to Lindley and Hutton’s plate,
the leaf-scars appear to be a little roughly drawn, their upper
angle being too acute and the boundary-lines of the lower
portion of the leaf-scar too convex. ‘Their reference to
Rhode’s pl. ii. fig. 1 must be excluded, as Rhode’s figure
belongs to Lepidodendron Veltheimianum and not to their
Ulodendron majus.
From the examination of numerous specimens, many of
which were in exquisite preservation, there can remain no
doubt that Ulodendron minus, L. & H., is only a slightly
younger stem of Ulodendron majus, L. & H. The reference
they give to Allan’s plate of the Ulodendron from Craigleith
Quarry, as synonymous with their Ulodendron minus, must
also be cancelled, as Allan’s plant is likewise Lepidodendron
Veltheimianum, Sternberg. I have carefully examined the
counterpart of the type of Ulodendron minus, L. & H., which
is now all that is known to exist of the fossil, and am assured
by the shape of the leaf-scars that it is Sigillarian, they being
in fact of the same form as that described by Romer in Sigit-
laria Preuiana ; but this point will be more fully discussed
presently*. The figure of Ulodendron minus, given by Les-
quereux in the ‘Coal Flora of Pennsylvania,’ and which
appears to be inverted, is not very satisfactory, but is probably
Lindley and Hutton’s plant. The same author gives an ex-
cellent figure of Sigillaria discophora, Kénig, sp., in the Geol.
Survey of Illinois, vol. 1. p. 450, pl. xliii., under the name
of Segillaria Menardi, where the character of the leaf-scar is
clearly shown. ‘The specimen he figures has been a compara-
tively old stem, but is very characteristic of the species. In
fact Lesquereux here notices the Sigillarian nature of his
* See p. 256.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 18
254 Mr. R. Kidston on the Relationship
fossil, and places it in the correct genus, but perhaps not
under the right species, though Iam by no means sure that
Stgillaria Menardi, Brongniart (Hist. d. végét. foss. pl. elvii.
fig. 5, not fig. 6), does not belong to Sigillaria discophora.
It is a little uncertain if the figure given as Ulodendron
majus by Lesquereux in his ‘ Coal Flora,’ pl. lxvi. figs. 3
& 3a, belongs to Lindley and Hutton’s plant. The expla-
nation of the figures is, | am afraid, inaccurate, if they belong
to the species under which he has placed them. He appears
to have had under consideration two distinct plants. Perhaps
his fig. 3 a is the Bothrodendron punctatum, Zeiller *, which is
not, however, the Bothrodendron punctatum of Lindley and
Huttont. The Bothrodendron punctatum, Lindley and Hutton,
is only a decorticated condition of their Ulodendron majus
and U. minus. The plant which Zeiller has figured and
identified as Lindley and Hutton’s Bothrodendron punctatum
is a closely allied species to Ahytidodendron minutifolium,
Boulay ¢, and it is interesting to find the large Ulodendroid
scars also occurring in Boulay’s genus Rhytidodendron.
Ulodendron punctatum, Sternberg, Vers. ii. p. 186, pl. xlv.
fiz. 1.—As this specimen is decorticated it is impossible to
determine the species to which it should be referred, though,
from the closeness of the foliar vascular bundles to each other,
it probably belongs to the Sigillarian group of Ulodendron.
Even in decorticated conditions of the so-called Ulodendra,
if the little “dots” of the foliar-vascular bundles are shown,
there can be made in many cases a probable determination as
to whether the specimen belongs to the Lepidodendroid or
Sigillarian group of Ulodendron, for on the Lepidodendroid
members the Jeaf-scars are larger than on the Sigillarian,
and consequently the foliar-vascular-bundle “dots” on
decorticated stems of Sigillarian Ulodendra stand nearer to
each other than they do on Lepidodendroid Ulodendra. This
is not, however, in all cases a secure generic test, and in no
ease will it lead to a specific determination. When the little
“ dots”? are not shown, it is impossible even to say to which
genus a Ulodendroid fossil belongs.
Ulodendron ellipticum, Sternberg, Vers. 11. p. 186, pl. xlv.
fig. 2, does not admit of any satisfactory allocation. Uloden-
dron ellipticum, Rohl (/. c.), pl. xxui. fig. 8, appears to be
referable to Stgillaria discophora ; but his fig. 4 of the same
* Ann, des Scienc. nat. 6° sér. Botan. vol. xii. p. 218, pl. ix. figs. 1-3,
and Véeét. foss. du terr. houil. p. 116.
+ See ante, pp. 188 and 174.
t Boulay, Terr. houil. du nord de la France et ses végét. foss. p. 39,
pl. iii. figs. 1, 1 hee.
of Ulodendron to Lepidodendron, ce. 255
plate is too indifferently preserved to speak of with any cer-
tainty. Neither can any definite identification be made of
Ulodendron Lindleyana, Rohl (l.c.), p. 138, pl. xxii. figs. 1,2.
Nor can one speak with more certainty as to the specific de-
signation of Ulodendron Schlegelit, Hichwald, ‘ Lethea Ros-
sica, vol. i. p. 138, and ‘ Urwelt Russlands,’ Hefti. p. 81,
pl. ui. fig. 4.
Ulodendron transversum, Carruthers (. c.) (not Hichwald)
(which does not, in the few characters that the fossil shows,
appear to differ from Ulodendron Schlegelii and Ulodendron
Conybearti, Buckland), is also probably to be referred to
Sigillaria discophora. Of course, in discussing the nature of
Ulodendron, absolutely nothing for the elucidation of its true
affinities can be learnt from such examples as those just men-
tioned, though, if at all possible, one is naturally anxious to
correlate them with the species of which they are decorticated
examples.
The small figure which Buckland gives of his Ulodendron
Lucasvi is not all that could be desired for a satisfactory de-
termination; but from the form of the few leaf-scars, as
shown in his figure, there is little reason to doubt that this
species should also be placed under Stgillaria discophora.
I am unable to discover any point by which Ulodendron
pumilum, Carruthers, can be distinguished from Sigillarda
discophora. ‘The specimen from which Mr. Carruthers’s figure
is taken is in the collection of the British Museum, and shows
very well the Sigillarian form of the leaf-scars. This fossil
is somewhat smaller in all its parts than Kénig’s example,
but this difference is entirely dependent on age. A figure
agreeing in all essentials with that of Mr. Carruthers, and
which I also refer to Sigillaria discophora, had previously
been published by Dawson in his ‘ Acadian Geology,’ 2nd ed.
fig. 170G, p. 455 (1868), under the name of Lepidophloios
parvus. What I believe to be only an older state of Lepido-
phloios parvus is the Lepidophlowos tetragonus, also figured by
Dawson on p. 455 of the same work, and in the Quart. Journ.
Geol. Soc. vol. xxii. pl. x. fig. 49 (see Pl. VIL. fig. 134*).
Halonia disticha, Morris (d. c.), must also be united with
Sigillaria discophora. Specimens preserved “in the round,”
similar to his figure, are by no means uncommon. The pre-
sence of only two rows of large scars on his fossil is sufficient
to remove it from Halonia (= Lepidophloios), and the other
characters of the specimen show its true place to be here.
Geinitz, in his Verst. d. Steinkf. in Sachsen, p. 38, appears
to have misunderstood the true nature of Lindley and Hutton’s
* See also ante, p. 178.
Loe
256 Mr. R. Kidston on the Relationship
genus Bothrodendron, for, under the name of Halonia punc-
tata, he includes different plants.
Lepidodendron salebrosum and Sigillaria perplexa, Wood,
are only fragments of Sigillaria discophora.
Both in Sigillaria perplexa and in the figure given under
the name of Stgillaria Menardi by Lesquereux, the longitu-
dinal clefts which appear in the bark of old examples are well
seen. A similar vertical splitting of the bark also takes place
in the succeeding species (Stgillarta Taylori, Carruthers, sp.),
and has already been pointed out as occurring in Lepidodendron
Velthetmianum.
One of the most interesting figures of this species has been
given by Rémer in the ‘ Paleontographica,’ vol. ix. pl. xii.
fig. 7, under the name of Sigillaria Preuiana. He says of
his plant, on p. 42 :—“ The leaf-cushions stand, as in Lepido-
dendron, in oblique rows; they are rhomboidal or six-sided,
as long as broad, slightly elevated, and show above the
middle a round scar, on each side of which are two semilunar
scars. The leaf-scar is almost as large as the leaf-cushion.”
I have seen many well-preserved specimens of Stgillaria
discophora with the leaf-scars identical with those described
by Romer as occurring in his Sigillaria Preuiana, and were
it not for the presence of the large Ulodendroid scars on these
specimens they could not have been distinguished from
Rémer’s plant. Hence, as Sigillaria Preuiana agrees in
all the characters that it shows with undoubted specimens of
Sigillaria. discophora we have no course left but to unite these
two species. Portions of some of those examples of Sigillaria
discophora, to which I have referred, might be broken off from
those parts where the large scars do not occur and would be
undistinguishable from Sigillaria Preuiana, Romer. I am
also strongly inclined to think that Lepidodendron pustulatum,
Boulay *, is not specifically distinct from Stgillaria disco-
phora, Konig, sp. Sigillaria discophora appears to be re-
stricted to the Coal-measures.
Localities and Horizons.
ScoTLAND—Coal-measures.
Ayrshire: Bonnington Pit, Kilmarnock (Rev. D. Lands-
borough.
Clackmannanshire: Devonside, Tillicoultry (7. Mitchell)
Furnace Bank Colliery, Old Sauchie.
Lanarkshire: “ Airdrie Coal Field” (Hunterian Museum,
Glasgow) ; near Carluke (collection of British Mu-
seum) ; Shotts (ditto) ; Shettleston (&. Dunlop).
Perthshire: Blairingone Colliery, 12 mile 8.E. of Dollar.
* Boulay, Le terr. houil. du nord de la France et ses végét. foss. p. 87,
pl. ii. figs. 2, 2 d¢s, Lille, 1876.
?
of Ulodendron to Lepidodendron, ce. 257
ENGLAND—Coal-measures.
Durham: High Main Seam, South Shields (Type of U.
minus, Hutton collection).
Northumberland: Bensham Seam, Jarrow (Type of U.
majus, Hutton collection).
Shropshire: Coalbrookdale (Zype of Halonia disticha,
Prof. Morris).
Staffordshire: Longton (J. Ward); Low Moor (collection
of British Museum).
Worcestershire: Bewdley (collection of British Museum.)
Yorkshire: Boldshaw, Bradford Moor, Bradford (collec-
tion of British Museum) ; Wakefield (ditto).
Sigillaria Taylort, Carruthers. (PI. IV. figs. 6, 6a;
Bl Vee Opi Vil tes. 105 106.c 5d.)
Ulodendron Taylor, Carruthers, Monthly Micr. Journ. vol. iii. p. 152,
pl. xhii. fig. 1 (1870).
Ulodendron minus, Thompson, On Ulodendron and Halonia,” Trans.
Edinb. Geol. Soc. vol. ii. p. 341, pl. (B).
Lepidodendron Veltheirmianum, Stur (in part), Culm Flora, pl. xxxix,
diese 2. , ; ;
Sigillaria, sp., Kidston in Cadell, Trans. Edinb. Geol. Soc. vol. iv.
p. 385.
Description. Branches dichotomizing; leaf-scars small,
rhomboidal, contiguous, their transverse and vertical diameters
being almost equal. Leaf-scars placed on slightly elevated
cushions, whose size little exceeds that of the leaf-scar; upper
and lower angles of leaf-scar rounded, lateral angles sharp,
but scarcely produced. Vascular impression situated towards
the upper part of the leaf-scar. Certain branches bear two
opposite vertical rows of large (Ulodendroid) scars, those of
one row alternating in position with those of the corresponding
vertical row. Large scars circular, occasionally oval, usually
separated by a slight interval, but sometimes touching each
other. Bark generally fissured by longitudinal clefts. Large
scar-bearing branches ending in a truncated apex. Decorti-
cated specimens also exhibit the longitudinal fissures and
show on their surface small “dots” arranged in quincuncial
order. Leaves single-nerved, lanceolate. Fructification
(sessile ?) cones attached to the vertical rows of large scars.
Remarks. This species is much smaller in all its parts than
Sigillaria discophora, nor do its branches appear to have
attained the same magnitude as those of the last-mentioned
species. The leaf-scars also are more truly rhomboidal.
The form of the leaf-scars is not well shown in the type
specimen of this species, but they are better shown in the three
other figures of this plant, which have been given under the
258 Mr. R. Kidston on the Relationship
names of Ulodendron minus and Lepidodendron Velthet-
mianum.
It is difficult to understand how Dr. Stur has included his
two figures of Stgillaria Taylort under Lepidodendren Velt-
heimianum, as no state of preservation or age could account
for the leaf-scars of Lepidodendron Veltheimianum becoming
so altered as to assume the form and arrangement shown in
his ‘Culm Flora,’ pl. xxxix. figs. 1,2. His fig. 1 shows an
older condition of Stgillaria Taylort than his fig. 2. The
right-hand upper corner of this last-mentioned figure indicates
clearly the Sigillarian form of the leaf-scar, and how close the
affinities of this species are with Stgillaria discophora. Mr.
D’Arcy Thompson has figured an example of this species
(Ulodendron minus, |. c.) with the lower portion of the appen-
dicular organ attached. The Clathrarian form of the leaf-
scars is well shown in his figure, but even better on his
specimen, which he has kindly lent me for examination.
I have already given a description of an example of this
species (No. 18), collected by Dr. Macfarlane, which shows
the appendicular organs in a young condition, attached to the
stem (PI. V. fig. 9).
This species is restricted to the Lower Carboniferous (Car-
boniferous-Limestone series and Calciferous-Sandstone series).
Localities.
ScorLtANpD—F rom the Carboniferous-Limestone Series.
Linlithgowshire: Blaes, 20 ft. above Parrot Seam, No. 6
Pit, Grange, Bo’ness (H. M. Cadell) ; Silver-Mine
Quarry, Linlithgow (1. M. Cadell); Bathgate (type
of species in the collection of the British Museum).
From the Calciferous-Sandstone Series.
Midlothian: Camps Lime Quarry, near Midcalder (R. F. B.
Bishop); Straiton, near Loanhead; Addiewell;
West Calder; Midealder.
I conclude by thanking the friends who have so kindly and
willingly submitted to me for examination many specimens,
which have been of the greatest use while drawing up these
notes.
EXPLANATION OF THE PLATES.
Pxrate III.
Fig. 1. Lepidodendron Veltheimianum, Sternberg. From Burghlee, Loan-
head, Midlothian. Calciferous-Sandstone series. Natural size.
(Specimen No. 1.)
Fg. 7.
Fig. 8.
Fig. 9.
of Ulodendron to Lepidodendron, ec. 259
PrateE LV.
Lepidodendron Veltheimianum, Sternberg. From the Oil Shales,
West Calder, Midlothian. Specimen in the collection of the
Addiewell Oil Co., Addiewell, Midlothian. Calciferous-Sand-
stone series. Natural size. (Specimen No. 3.)
. Lepidodendron Veltheinianum, Sternberg. From Dalmeny, Lin-
lithgowshire. Calciferous-Sandstone series. Natural. size.
Specimen collected by Dr. Macfarlane, Edinburgh. (Specimen
No. 4.)
Lepidodendron Veltheimianum, Sternberg. From West Calder,
Midlothian. Calciferous-Sandstone series. Natural size. (Speci-
men No. 5.) "
Sigilaria discophora, Konig, sp. From Furnace-Bank Pit, Old
Sauchie, Clackmannanshire. Coal-measures. Natural size.
(Specimen No. 15.) 5a. A few leaf-scars from fig. 5, enlarged.
Sigillaria Taylort, Carruthers, sp. From Camps Lime Quarry,
Midealder, Midlothian. Calciferous-Sandstone series. Natural
size. (Specimen No. 16.) Collected by the late R. F. B.
Bishop, Hsq., Edinburgh. 6a. A few leaf-scars from fig. 6,
enlarged.
Srgilaria Brardu, Brongniart. A few leaf-scars copied from
Brongniart (Hist. d. végét. foss. pl. clviii. fig. 4).
Puate V.
Stgillaria discophora, Konig, sp. From ‘ Coal-measures, British.”
Specimen in the collection of the Geological Survey of Great
Britain, Museum of Practical Geology, London. Natural size.
(Specimen No. 13.)
Sigillaria Taylort, Carruthers, sp. From Calciferous-Sandstone
series. Natural size. (Specimen No. 18.)
PLATE VI.
Fig, 10. Sigillaria Taylort, Carruthers, sp. From the Oil Shales, near
Addiewell, Midlothian. Calciferous-Sandstone series. 2+ natural
size. (Specimen No. 17.) In the collection of the Addiewell
Oil Co. 106. Small portion of stem, natural size, marked 0 on
fic. 10. 10c. Ulodendroid scar marked ¢ on fig. 10, natural
size. 10d. Small portion of stem, marked d fig. 10, showing
the Bothrodendron-condition of the plant.
Fig. 11. Lepidodendron Veltheimianum, Sternberg. From Blackbraes,
West Calder, Midlothian. Calciferous-Sandstone series. 3
natural size. (Specimen No. 6.) Collected by J. Linn, Esq.
lla. A few of the leaf-scars, marked a, fig. 11, natural size.
11%. Profile view of appendicular organ, which fits into the
depressed Ulodendroid scar of fig. 11, natural size. lle. Basal
view of appendicular organ, natural size.
Prats VIL.
Fig. 12. Sigillaria discophora, Konig, sp. From Devonside, Tillicoultry,
Clackmannanshire. Coal-measures. Natural size. (Specimen
No. 12.) Collected by Mr. T. Mitchell, Tillicoultry, 12a, A
few leaf-scales from part marked a, fig. 12, enlarged. 126. A
few leaf-scars from part marked 0, fig. 12, to show variation in
form of leaf-scar, enlarged.
260 Miss 8. G. Foulke on Chilomonas paramecium.
Fig. 13. Sigillaria discophora, Kénig, sp. From Furnace-Bank Pit, Old
Sauchie, Clackmannanshire. Coal-measures. (Specimen No. 14.)
Lyaturalsize. 13a. A few leaf-scars, natural size. 156. Small
portion of fig. 13, showing Bathrodendron-condition, natural
size.
Fig. 14. Lepidophloios seoticus, Kidston. From West Calder, Midlo-
thian. Calciferous-Sandstone series. a, articulating leaf-
surface ; g, downward-directed cortical cushion.
Fig. 15. Lepidodendron aculeatum, Sternberg. Leaf-sear, to show its
various parts: a@, vascular scar or impression; 6, vascular-
bundle impression ; ec, the “field ;” dd, oval pits ; e, “ligule ”
depression ; 7, medial line.
XXV.—Chilomonas paramecium. By SARA GWENDOLEN
FOULKE*,
[Plate IX. B. figs. 1-6.]
SINCE its discovery by Ehrenberg this form has been carefully
studied by Biitschli, Stein, and Kent, the two latter giving
the first entirely accurate diagnosis of its character.
According to Kent Chilomonas is classified as follows :—
Order Flagellata-Eustomata; Family Chilomonadide ; Genus
Chilomonas.
Fig. 1, Pl. IX. B, represents the form so accurately that
no detailed description is necessary.
Biitschli states that this animalcule, when isolated for
observation, quickly loses its normal contour, and becomes
spherical, finally disintegrating.
While I was investigating a drop of water teeming with
Chilomonas a minute flagellate amoeboid form (fig. 2) entered
the field, and after swimming uncertainly about for some
moments, settled to the bottom of the live-box, where it
moved in ameeboid fashion, the two flagella becoming merged
in the pseudopodium-like processes. The presence of about
twenty small highly refractive bodies, suspected to be germs,
was noticed. Soon the mass became so diffused as to form a
mere film, and presently disintegrated, setting free these
bodies, which swam away. Several similar individuals were
found, some of which, on becoming quiescent, took a globular
shape, retaining both flagella to the last. ‘This sphere then
erew larger and its wall thinner, until, like a bubble, it burst,
hberating the germs, which were always present and very
* Fiom the ‘ Journal of the New-York Microscopical Society.’
Miss 8. G. Foulke on Chilomonas paramecium. 261
active (fig. 3). So many of these forms were now found,
while the number of the adult forms of Chilomonas at the
same time diminished, that the identity of the two was sus-
pected ; and the suspicion was verified almost immediately by
my witnessing the transformation throughout.
An individual would begin to spin round, gradually losing
contour, while the refractive “corpuscles” ranged near the
cell-wall left their places and moved actively about, showing,
as did also the increased transparency of the cell, incipient
liquefaction of the endoplasm. An amceboid character was
now assumed, until, finally, one or the other of the two phases
above noted was entered upon. When the final shape was
that of fig. 4, the freeing of the germs was effected in various
ways. Sometimes, as stated, the film became generally dis-
integrated ; in other cases one large external vesicle was
formed, leaving only a very smail portion of protoplasm
enclosing the germs, and from this the germs energetically
freed themselves after the bursting of the vesicle (fig. 5). In
still others a small vesicle formed about the germs, and,
moving to the cell-wall, extruded itself and burst, liberating
the germs directly into the water, after which the remainder
of the animalcule disintegrated (fig. 6).
In from four to five days each of these germs developed
into an adult Chilomonas, having the characteristic form at an
early stage of growth. The ‘“ corpuscles,” or, correctly, the
erms, appeared in these at maturity.
The habit of breaking up, as recorded by Biitschli, probably
coincides with the above phenomena; and although that
author does not describe the liberation of germs, I believe
this habit to exist principally for that purpose, as the young
or recently matured Chilomonas was not affected by confine-
ment. ‘his, then, seems to be the first time that the true
character of the ornamental belt of so-called corpuscles has
been indicated.
The transition to the globular and the amceboid phases
afforded strong corroboration of the opinions of Stein and
Kent, as opposed to that of Biitschli, regarding the point of
growth of the flagella—showing them to be inserted close
together.
Mr. A. H. Cooke on Testaceous Mollusca
262
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263
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Mr. A. H. Cooke on Testaceous Mollusca
264
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265
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\. H. Cooke on Testaceous Mollusca
Mr.
266
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-W09 8B eSODTI]MA ele suottoeds Suno XK
‘S[LOYAL Moy 4svy ory AT[ereues yv Aydnaqe
sdoqs SuIq(it [eUIpNyLsuoT ey} MOY AoYs [ ‘BAe JO o]S] ‘IN, pus yuLog
jou soop puv “peq AoA st oinsy seacery |uppelg] -eyeysny ‘sourddyiqgjoyiez ‘eroys ‘$quenboaq |‘: *:'
"MOOT “OUD oy} Ur “Sy ‘{UIOT 94107,
§oAeey Ul Uv} pesnyye alow you dry 103nG -ereqgsny ‘sourddipiyg |‘eroys ‘suoutoeds omy,
TE TORO MCPS "HOTYEIS
“ nounr “eyequepity am
‘PP ‘VW ‘eyeayVlO VUTOSSTYT
‘mog ‘eqvatds
‘a CIOSSIYY
TUS
a
267
n~
wo
obtained in the Gulf of Sue
‘TITAN “9 ‘vurnouooopnasd ) sotoods oy 10%
(996 ‘€ ‘TERT “8 'Z *d) ‘PY “VW Jo vuenouos
pmossyy 841 OU St serdeds sty} 4VqI 930 NT
‘punossy BA\-9Y}-Jo-Jno suvoeut Aue
Aq you & Jo T[eYs MoM pue Suno0d vB Jo yno
‘snuecqns Mou v ynq ‘soroeds Mou B ATareut
you oyvul 0} “IoAeMOoY “tapunyq eTqrtte, B
SBA 47 ‘[NFIQnop AeyIwI snues oy} epeu
S[IOYA Tvorde oT} Jo ssor oT] FVYY ynq ‘(esod
-dns 7 odA, mewohyy oy} Jo) pryeprmettg
B Jo qoodse of} pry Teys oy} ey} SurTo0Ty
“wow smupy “TET ‘d “TA ‘O28T “HN “StI
H UUW SY} Ul pedimsep sva 4p “4ys8TI
eymb stey pur ‘morpuyorpy sojou ,,“ngn.uds
pudoss~r JO UeTAIOAdS UuAyoIG puv TOM v
ULOA, Pogttosop woaq eALT 07 sty} yoodsus T,,
‘(ee1 ‘d ‘OL8T “HN “StI
UUW) vpeund toy oyvISTUL eo VB SI DpnLUNIT
PHEML rOes
[[ts (vpyyaw Jo asvo OY} UI oANNs 4v spIOTAL
10 UOlRNSue pure stxe Jo uoryesoy1ed-aou)
seouorleyip pojdmeyye suepy ‘waoF
LOYsorf oy vp ‘ssoperjsny pur TIOA\ 944
Suteq puurouoo ‘surpooatd ot} YILA\ TeoryUEpyT
‘aT ‘d ‘tA “OUST “ISTH UN “SUIT
YN UNV UL SoULMOT[OF oY} ITAA ‘poqttoseq
‘yy.orr og Av UOTyLOyTUEpt oy} Vy} ST
pres oq Uvd yLY} [BV pu ‘WIAA ST TOYS OT,
‘SLI at} TAM 10q
poyerys ‘auassyzra jo proysut ‘Apsu0I4s
sureq pue _“eucfue synuds snpnowny’,,
oy} jo usis Aue Sutavy you ‘o7ay200g
moi youystp oyinb ore Aoyy, ‘Surpeo
-ord oy} se ommes on} ore suompoeds osoyy,
¢ DUnLUDIDOS Sppe "Py
"VY Yoram 09 ‘saprowmppos pure ‘sru.l0/r.107
-nas ‘pyjadnnas DOSsNT PE IIOSEP "PW “| ‘O
“SS vl er
eoebeeacsee eee see
‘JIM.H urisiog, ‘uedvp
Se@eee ee ee oe eee
eee eo Bt eo wees roe
err oe ee ea Be eo we
“[Lanl Coog “eyet
-ids eutossny=] ‘pr
[‘uommtoeds ong ]|'7 “euutouoo vuupeysosoryy
‘pp “yr
-nd] ‘pr ‘7 ‘emunjd ——
eotoeeee
Ley ‘Py ‘ep =]
[‘uomtoods eug | |py py ‘euuram09 ——
[‘suemtoeds omy |['*°* py y “eprytu epedyy
‘uotmtoeds omg |'*"* “pyg “eeeatyAra ——
“my, [pr ‘Vy “eyo
FINH Ueisiegq, |pue yulog o1e7 ‘oe1vt 4ON|-1[d] ‘ynzr ‘yoyoyjzogq ——
Mr. A. H. Cooke on Testaceous Mollusca
268
[‘sqrenig
samtoy, ‘vIpeajsny ‘Bp N] ‘seurddrprygy
‘sourddyiyg
@ WIOy
asIv] B uBy} etou suryydue ‘(opreppy)
‘py ‘VW ‘vinn) ‘@ 8 ‘eT qeyeqgstuun ynq
‘odAq oy} uvyy poonpord o10ul req} eZ STEYS ‘JNO urisieg, ‘ueder
‘urdep
‘rede pr
‘ueder
‘under
‘ude pr
‘aude p
JMO UeIsied ,
FIND wWeIsIed,
F[Ny) UvIsSLo “
‘under
‘angus oT}
ye oul, pepreq wv ‘posnye reyyea dit 10yno
TeAo suoy Atoa vB JTey AYovxe Suteq You
oy} “yueseya ATeuredyxe st [Joys yuoserd
on “qUOW, ‘wym.us= yorga “(Tey “d
‘reeproq Vy “TOW) Avtarpisovyy, Jo seponwh
‘7 B SI o10Y} SB “MASQYd-[[I se OULVU OTT,
‘s[LoyA doy soz O14
JO moydesxe oT} TITM sooerd 07 poyserus
ueeq AjoyvunjLojUNn sey uewmioeds opours OUT,
(6 “8y
‘9 ‘d ‘[10IG ‘AONNY “48e7,) 07eSOIO] TOP,
Jo puumouos vossnr ey} tou ‘g ‘ds ‘vossear
‘OT ‘qou0g ‘assoy ut “py ‘vy ‘ouma
-09 SB poInsSy (Lo}snyy UL FNVYUIO AA apra
“SH IVULO YT “MOTINGIASICT
‘pues
“uqey ZT ur ‘suetmioeds mot
‘suomloeds saTq.y, |**
"anaany
‘gaplolie[os er1oydouex
‘H CINIMOLLVT
‘py ‘Vy ‘vyouloons ——
‘uowtoeds aug |'*** ‘py 'y ‘styeanyns ——
‘yuonbeay |’ °° °° py py “VIVA eTRI(; |
‘uatatoads ou |'* "pH PY feprony |
‘OIBl JON |' “pp “VPROLIqUIL VqeLY |
‘momdeds oud |** "py ‘Pp “vyoutoojnt
‘quonbor 7 ‘py ‘Vy “eyetnoyexr ——
‘quonbeta | "°° “pp py “erqvos —— |
‘quonbey | pp ‘y ‘septodnd vijoue,y
‘suourtoods ano,q
‘aoutoeds ong
‘| womtarr |
Py ‘“y “BtoptTUL BqoUu()
"+ pp ‘py ‘siptoeLd Bossi]
‘uetatoads auc) ‘pr ‘py ‘elafI[No1Egny VUELOKD
*suetmIoads OA\T,
TOL
‘op py “epnsrdd erye1e)
|
|
269
obtained in the Gulf of Suez.
“0L0YUD 4A
SB TONUI sv 4SOMITe Ive ay} spUayyo ‘snes
B jo owen oy} sv ‘unssog ‘*y-geT ‘dd
‘esl ‘Q'Z'd wl ydeasouom ssuepy
"Vy jo optds ut ‘wmssoy yom ‘snumsso.7 OFT
[I ‘pueq jeorpiquim-vor oy snd ‘omg
ATWO sey SIq} “[LOYA 4svT oy} UO anbu0
OAY Sey siwwayyo012 ‘poyruept Apsuor AA
*TLOYA 4SVT OY} WO sqrt FO oynqzTysep
AjoyoTdtm09 ove saetmroeds uMo1s-]pNy sour}
qoyyo 4B ‘poyencuy pue odie, exe sqtt
oy} suoutoeds [[ems ut sotmutyetmos {aTqe
“IVA ATOA ST SUTGQGIX ey, ‘JauIK, ‘wagoap
SNYI0.67, UWMOUY-[[9M OY} JO (orIVA qT v
UBy} GLOW suTYyZOU om 07 stvodde sotoods oY J, “TEN “eTaOpoyeg MON |
“DYDYO) UP UCI pUyT,
-180,\\ 9} JO ,, ONsopvur ,, UeIpUy-jseyy ONL,
"JIMS AMOT[OF 07 GARY TILA
(njoortog.in “ynogagy ‘numddipnysz) sevoeds
UVIPU-JsVyy SeAeex] JO Lequinu vB ‘y.ugnos
Jo Ajowwa poyreut v oq vualynbun jr pue
‘oS J] “Blgquvos OjUL Soywnpetd soroeds sq
yey} worordsns oy} proav 04 “toy3090} pored
-uroo ore “wey ‘pwafynbun wa0y 94} Jo
dequinu Aue wey “4[noWIp st4y ‘sotoods
1o}}8] 9y} FO sommgvoy Surysinsuystp
AI9A WOES BITOUMTOO MAO PUB WLOF prTOs
arom eyy, “wAuouds v ‘eaoory “equuooma,r
SuLepisuvo ut ATUIe}1e9 Os THIY. AXOT[OF
ATpxey pmnoys J ynq “(ge -d “Zest “qe
‘youoy “uMmeYyD UL) YNeyure A, Aq vV.Lgvos
UUIM poyizueptT Apyyport Us9q SVy vIpauULlaquy
; 2 pecs. a cor Oars & —
Lev
‘py ‘snyeurreoiq| “pyr
[‘yemimg ‘nseq] ‘sreg m10qseqy ‘uotutdeds emo ‘exomg | “77 ‘stteayqo01. sn.aesyo aT
‘aroys ‘yuonbeay |* °° *zassy ‘tpuoustg vyjasty
[Tle ut sueutoeds
[eyensny joatq] ‘qyey Pp “eaoo uo |-[-tea ‘yous ‘mny90} = |
‘ST TOL pug | curary ‘uemtoods ouo ‘areyy | gag ‘snprpueo Sn[NpoyAy
“poulUloyey sey + guep
"BOQ poy |-Unqe ‘syreut-opy weeMyeg [°° "* “py ‘esopouqns ——.
*POULULOY VAT SVYy
"B09 poy]: oret “syreM-epy woomog |'*** ‘py “euvaseyprar ——
[eyersny “a's ‘eyeny Topfeg | ‘oxy ‘permutoy, ‘L-7 ‘eaqeos = ]
yey, ‘sourddyiag ‘puryjoyy Mot |-ep sexy {orer ‘roqem MOT |'72Y¥q “SIpetiteyar vuLt0z4IT
°
- XVI.
Ann. & Mag. N. Hist. Ser. 5. Vol
Mr. A. H. Cooke on Testaceous Mollusca
270,
torreysod oy} 4eq} os ‘uLsreut ey} IdAO
qsouye st “Quourmmord [7B 4e you st yor
‘xedv ot} qvy} Jovy oy} puv ‘tutoz snoqqra
AOA OT} ‘UONBASTA OUME1}xX9 oY} ore seINy
-vey AYYIOME}OU oT, “Mog ‘vpMnIUW) 8B
odd} omnes oY} JO ST [[EYS o[qeyavmo.t SIT,
‘UL GJG. “UOT “UT
Gg. “‘FTB fosuo;qo eutuer0; ‘styefNoT}UEp
opl[ea snjzUT snqtursrvur ‘oytsod ‘vayyn det
‘tueto1te}sod teuts.eu eadns sorde ‘eye]]90
-U¥O SIOLIJUSOUOD SISTOASURAY STITT ‘YyeTPRA
snqitoleor eu1ey[e sisotswna stjs00 ‘ourp
-nyLouoy enbye ourpnyyye exey vende ‘eye 8400)
-noreted “esoqqis ‘epiqye “eyvAa[o Bq80} “ssyT BOO ODS 09.0.0 bb [ ‘smemmroeds mo, | ‘umjueuntpe dot
‘quvqjsuoo sAva\ye you are sXvx yrep IMoy
omy yorys. ur ‘eyaddnay osye st Morpuy
vy Jo ,,quenboayz ‘10yva MoT ‘ds 99
ey, ‘wey seyun (got Yor ‘s8y ‘nppae
-rssiy ‘Snaneseyy, ,) Aqiamog ‘streddesrp
eTAIOYIP SITY} WAOF IMpe oy} ut ynq ‘eddy
oY} SB pozoopos ey UemIoeds aq} UI Soop 4I
: SlaYIp soyito og} sAvs oAvoy ‘wAuouds
vw st ‘(sourddriyg) osvary ‘nynypv.uuponey [soutddyryg] ‘vog poy ‘quonbery SeroyG | “og ‘myjeddnyy eppernsstyy
‘KH CITIGUASSI
]
“SYD. 16
Syv.4ysnv Jo suauitoeds payea [honey ‘stpexy
“99 LOTJVI ULY} sOW suTYyZOU ere oso, SUKIDETOULOOO ‘suotmmtoods omy, -sne] ‘pp “Pp ‘voruod
“wmypla) % * -yuenb
2 uo ¢ 3
IME EES HG) SUCTION ‘BYCasny |-orsun you “YZeF G 0} a10YG | Aon’ ‘stpeajsne voyy;euLy
PV
‘uotutoeds ug | “esojnuers sedoejopyoog
‘anaay
‘sourddiiyg ‘oroys ‘suemtoeds omy, | “ertozromsop vena dteg
‘H CICULIATVO)
‘SYIVULO YT “MOTINGIySI(T "UOTIEIS TP4S
“YouoH ‘umeyy Ur uoydrMosep pur omsy
B TO popunog svar Tory ‘(FOL “d) “qT
‘nsiur myaing yueserdat 04 pesoddns
‘Ayiqeqoad ype ur ‘st WOOeT[OD Imo Jo
“AMTTICL ‘nssiour “binuisy OU], .—: SMOT[OF
SB OUL 0} soyLIM TYIMG “Wa “AT POT
OF SOMOIAFOL UL “FU “snyY ey} UL yoTqey
B WOIF MoIpuyovpy Aq poyruept yqnop on
"ayry
“SIU tos st oie, Suryurqy djoy fontnes
T Wq ‘somddiprgg oy} wor ‘snpy “yg
oy} UL BATS st “TT ‘nnssxg “soroods But
“AOT[OF OY} FO suutoF cunod ore payruopt
snq} (sueuroeds qyeus om) s[jeys ony,
‘FMI, ‘SNP oY} Ur are YZOq
jo sed&y oy, ‘wuouds v oq 0} savadde
(98d ‘Test ‘S°7 "a ‘orodesug) ‘py -y
‘ypjnund yorya Jo “(eg d TEgy ‘a7 "a
‘sourddipryg ‘ooutog) ‘py “yw ‘snadfijo ome
Aoyy, ‘wpmznzy you kpureyx90 oe s]eys
quaserd oy ynq ‘TaAWYR 07 e.mjUeA you op
I 3921109 oq MOTyeOyHUEpr ayy TOYIOT AY
“TRoUBIIOUpay oy} jo yaed AtoAe ut
punof st Yor “rAeg opumzmeT YALA (“xix
JOA “WOoT “YouoH) sdcsay Aq payruepy
‘potaaoostp yok suemmeds ATUO ot}
eq 0} awodde ypoys quesead oyy pue (Cenpy
‘Iq emg ut) edk oyg, ‘edoory sXvs
« UMOUY OU SI TONdeT[oo ueLsuIMUND oy}
UF TOYS eyqeyremer sty, Jo Aq1;voo] oyy,,,
271
obtained in the Gulf of Suez.
‘g]O.119 o}oTdm09 ysouye ue UWIOT
SUISIVEL 9Y} YeouLepun wor; PomMorA
‘avmnorpuedied ysomye st [ays ey} Jo pue
"ARM a ett inne, —~
['Ajjeqoues uvouvrreztpeyy |
eeoe ee ee oe oe eo oe
[‘sourddyrqg ‘oourog ‘orodeSurg]
eoeese soe eee te ee
[sireng
solo y, ‘vpersny ‘y'N) ‘sourddrypryg
FIND WISI Tx
‘[mysog ‘eqe3
. [suemeds tno] |-uopa] ‘aya “esstout, ——
19#
[29809
SE SESS (it ‘eyecuoe| “7 “ernssyy. ——
WPomseome Caner
(Ne ae)
‘peep ‘stountoeds seayy, |-AJo | ‘pny TIaTAN()
‘PE
‘Toultoeds ot ‘yy “eimsriour vynursreur
I O| VF four Bynutl
‘uowtoeds eug | ‘pr ‘Pp ‘eqyrsmbxe epnury
‘uemmtoeds omg |'* “py ‘zy ‘eueu, vitouleD
‘peop ‘oroys forey | “pp Pp “eureeSour
Mr. A. H. Cooke on Testaceous Mollusca
272
-ejo puv dn payoutd soumjottos ‘serjortes
oy puv ‘utoz yeordd, oT} se popaescot
eq Avut yorya ‘Lon’ ‘sypysrp woeajog
TONoUTysIp Suysey Jo ourqyAue gAtooted
0} efqvun we T ‘sotoods jo roqunu vB
OJUT epRUt Voeq seq SSULSPOT SIT 04 SULPIOD
-ov sodeys jo Ajorwa v sovunsse AT}uenb
-estoo YoIyA pue “[eIod JO sadtjsieqUL
SUIGVGUL YOU Teys vB “WeyZo O8 sk ‘oLOFT
‘9d OST ‘SZ 'd
‘sorloods mms oy} UL ATqBIopisu09
Aiwa 0} punoy oq T[AX ‘poulurexe eq swat
pads jo toqmnu jyuooyns wv jt ‘xede
ay} jo uoyrsod oy} aynubumugr wencoartt
pus osxey osey} UL ynq ‘apis ro1te}sod
ay} tervou st whuuung jo xede oy} yey
puno1s ey} wo ‘uoreredes @ toy spreyd
(ir ‘Joa ‘sninesoyy,,) Aqteaog “qseq
‘(satdoostt eAcoyy Sv ‘nznjngnos you) vpn]
~jagnos pur “mog “ahuwuwng Yt Rory
-uapt st [Toys oy} $6 OY ‘vudns yn °*S°7
‘soloads Surpessons oy Jo
urioy Sunod ev ATodout St uotmtoeds oe, 5uts
om {g ag m Td ‘or d Gzs1 ‘SZ 'd
‘ZENG
jo JNH oy woIy osoyy qyIM ATpovKe
gorse “ox Ysvoo ystuvdg oy} ‘stung, 48
morpuyovyy Aq pozoetjoo sueutoeds pure
‘seroeds ULoUBILO}IPO]Y MOUIWOD @ ST SIU],
(er 3g 4 3 ETT dT org Tow wan u Gy
TY api) wysog ‘obuoja 7 ey ere
Koy], ‘ST PULPILRT OU Woaz oq 07 pres st
‘roAoaToUL ‘Torts ‘setoeds yVy} WILMA oa15B
‘rorutdo Aur ut ‘toAeaoy “JOU Op sTPYys 1¢)
‘O-GZGL S80 “261 + ‘GBI “d “1x ‘TOA ‘qeQ
"Sy IeULOY
‘soutdd yy ‘SoTJOMeA [eos ‘el0Yg
Peer titeca: at ae se aria GEG
ove er soe eee teeoe [-uourroeds ou |
eer eter er re oecoee [-uountoeds ou |
" LOTINGLYSI(] “UOT]RYG
‘| hong
‘stpeaysne=¢] honey
‘sisuerqued vULO4LOLO ET
“opr 7 “epIpuea B4Se NT
‘Lysog “eyeyjoynos= |
Dp ‘Ay ‘esoont, ——
‘Lysa
‘eyeyjoynos= 3] “PY
‘7 ‘eysopowWy, evNULoTeUTT
— a : a 2 ai = tai ects etn edhe teteenasssinentntahia ttt RS eS
273
obtained in the Gulf of Suez.
ee ee a oe ee eee
sq} yey Vopr ou eavy T SSW “Ysed
‘naoay ,, 0} pojoattoo svy pur ‘Sucim svar
“MOS “Luyojg yey) peatsored morpuyoupy "W383 OS-OL ¢ eter oN
[‘sueuntoeds x1q]
[‘sqreryg soatog, “7 Loy
“ureg] “FNg) aersi0gy ‘sourddyryg
‘SUIVIYG
"BATE
"YIBJ OG ‘Uatutdeds oud
seloy, ‘Bipeaysny a ‘uourttoeds 9c
"D400 TTB ale
«, PeurMtayepun ‘satoeds oay,, ayy, ‘shea
PBOTG OA} OJUT pedsefeod oavy 07 suoddey
SULLLVUL OY} YOUA UL 70. JO sT[ays UO
“To] VAL
nq Suryjou ! paynueptr APSuorm oymey
‘SBaS BUTT |A\O] pue Torq uoamyoq ‘ervry
“IOVVAM ALOT
‘suomtoeds Ayyc10 noqy | [‘snyuMeyy ‘uepy | ‘onbiqurezoyy |pur [ory weaajoq yuonbery
“TOMUBUL ATLOSVUL B UL sna [OYA oy}
GHA s[vep YOLyA sponse ue ut senfun pue
snyohnt.09 $0 AY MApLay} poyeajstoutop sey
(196 ‘seg ‘dd tr joa -youog Jo ‘uanos)
Gug “VT I ‘pue qorteyue oy}
SPIVMO} MOTIVE srgnINUD.LA JO ESOT} OTL AL
‘sngpbin.t.009 JO IYSTIAJOVIRID B aq 0} SUTdES
Gory “Joypeavd pue yysteys er sopis oy,
[adoyy
pooy jo edep ‘reqizuez ! vipeaysny
TN ‘Avg mojzeropy ‘u04.8urss4y
qtog ‘urdep ‘eur ‘puvjeay may
"pour
‘guroqury ‘Aequatog |
‘sourddyiyg |-moyepy sey “peop { orey
[‘suouttoeds oa, |
‘quoserd 48 41 eqitosep you op [Inq {Mou :
steeddy someds oy, ‘{poynuepr ATSuoa M ;
‘ayeredos ydo¥y oq uvo 41 Joyo A
qqnop J ynq ‘oanydqnos reuy yyIM uTLOF
qeTems we st ‘Kon’ ‘sesuayung “py ‘Ww
"peep ‘sueutieds oerq 7,
-vie) “Mog “Leyolesy
‘PR Ay wuqnutiuty,
"“moy “wunyrpodimesy,
Yyoswy “wungenbroyqnsy ——
‘[ayoo ‘un104 |
*aaaay “TaNS.101}L.5110,. ——
qmoy
‘TANJRM.SueKXesTq WMNITB}UE(T
‘HW CIIV INGA]
‘[wway9
“eyoa | aaaagy “eyerpeatg ——
soars ““uUMayy) “8401 BI[9}eq
‘WALTIALVY
: ‘(7 ‘smsun
=aaaz ‘snyesnat00 |
‘nag ‘Snyepnuers snqynog
‘ddnay “eatqeie, ——
‘aspag “By8{[90TBd BUITTEINIG
‘oypowiqua se no peards soturjomtos “py
“y “nsojnpou “py “Ww ‘syudynos se “paqea
Mr. A. H. Cooke on Testaceous Mollusca
274
49 SNQTA] SITJYSIE}UT ‘snqIMedsouBAE 40
sngTUeose[voo Westde pe sysoo “ezvonbvy
STJOULSIP WIseq PV Pes SIYVASTO XIA ‘snqr7
-urysipinbes wou ‘mroepronyenb 1eyteato
stjsoo ‘eyenore wnaed ‘epronqpedqus ‘eyrpod
ee aioe Tatil eames euler
v ° v ry v =)
‘our, weyruts B Aq
poqoesiq AT[BIAUES SOATESUMAY} OLB TOTTLA
‘sqrt OY} 0} JoT[vted ore Loy} ! poyweur AoA
IW SOUL] [BYLS10JUL oy} Sustupoeds Ysorty UT
‘UL GZ. UIsvq pnde
‘ger SUL GJ.[ “suo, forsejut ootde ‘sityes
-snoep SISOASUBI} STUMIsSTFRUTUL onbstiys
‘sHROUIT JoPTVUIpNyLoUOT sIsdt s1}s0o WOU
-90U SII}tsiojur ‘yyvenbvy snqiyuezsrpmbes
‘snqiueutMe aprBA ‘sIyByNcuB uwWosoT
sysoo “eyeamnd snsiaA woody ‘eyeutut
-noe ‘voutoons aprjed “eprjos vse} “zeaqy
‘jueuItOId pur pexyreut
Azoa ore Loy} pur ‘our sAvaye ore oro yy
wngpjoauy UL eptqs ‘arnosqo ATeATyeIdtMo0d
aIB puv ‘UeASTO UBY} SSe] LOACU OAV SqTA
ay} PaaAINo oLOU SI [Leys SIT, *aMgdynos
S}L UL Sop|tteser A[SUOI|s SsefoqJoAou 4L
Yor ‘soroeds 4xeu oy} WOdF JOUTYSTp Ato A
‘UL G[. WIseq
pnde yey “ur Gt ‘“suoy forseyzur ootde
: sissorduut “tonqunb coztorto Wn.L0T}1}s.10} UL
Sle, ‘“SIBEUIT deyIAOZ Lo} [BULpNyLsuoT
sisdt s1jsoo VOU dau STI}YSKe}UI ‘vyvonbey
SHOUNsIp pes snqiyavy vunaed wupoeponp
OpoOUl ULLOEpUN OpoUt sysoo ‘yyENoIe ‘vyBU
-r1uinoe ‘voutsons eprjed ‘eptpos vyseq “zuaqy
‘QUO POO B ST TOTAL
‘soroeds oy} oqtiosep [[IM os ‘0} siojor
"SYIBULOIT
Ce ee [‘uewtoeds aug | [‘ayoo) ‘gnov — ]}
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Testaceous Mollusca obtained in the Gulf of Suez.
276
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Ul pu Jequinu ut yyoq Azpcurpeco
*SyIVULOY. “MOL|NGIAST “HOT}LIS TPIS
On Sponges from Sauna stralia. ATCT
XXVII.—Descriptions of Sponges from the Neighbourhood of
Port Phillip Heads, South Australia, continued. By H. J.
Carter, F.R.S. &e.
[Continued from vol. xv. p. 821.]
For ready reference I will also here insert a tabular view of
my arrangement of the order RHAPHIDONEMA, as I shall take
this (probably my last) opportunity of offering such revisionary
remarks on it as my experience since it was published in 1875
seems to dictate. It is as follows :—
Order TV. RHAPHIDONEMA.
Families. Groups.
1. Digitata.
2, Palmata.
Reptata.
4, Spinifera.
5. Tubulodigitata.
6. Aculeata.
7
8
1. Chalinida
. Subaculeata.
. Ciliata.
9, Bivalvata.
2. Cavochalinida
Ce Ce et
. Complanata.
. Plicata.
. Solida.
. Clathrata.
. Dictyalia.
. Digitifera.
. Fistulodigitata,
8. Acervochalinida
4, Pseudochalinida
The diagnosis which I have given for this . order—viz.
“‘ Possessing a skeleton composed of horny fibre with a core
of proper spicules. Horm of spicule chiefly simple acerate and
chiefly confined to the interior of the fibre,” —is too short and in-
definite to lead the student to the more useful or distinguishing
characters of that kind of sponges which the order is intended to
comprise, whose typical structure, to which I shall hereafter
more particularly allude, may be taken from that of Chalina
polychotoma, Esper. What this type is we learn from John-
ston, who, with a specimen of the British species before him,
identified it with Esper’s “Spongia polychotoma, tab. xxxvi.”
(Johnston, Hist. Brit. Sponges, &ec. p. 94, pl. iil.).
The name given by Johnston to this sponge is “ Halichon-
dria oculata,’ which Dr. Bowerbank changed to ‘ Chalina
oculata”’ (Mon. Brit. Spongiadee, vol. ii. p. 361), accompanied
278 My. H. J. Carter on
by the statement that Dr. Grant, in his ‘ Tabular View of the
Animal Kingdom’ (1861, p. 76), had established the genus
“Chalina”’ for sponges possessing the structure of Johnston’s
Halichondria oculata (Mon. vol. 1. p. 209) ; so this is how we
came by the term ‘‘Chalina.”
But Johnston had previously idéntified his foregoing species,
viz. Halichondria palmata (op. cit. p. 92, pl. 1. fig. 1), with
Esper’s Spongia oculata, ‘tab. 1.,” and also with Ellis’s Spongia
palmata (Ellis & Solander, p. 189, pl. lvii. fig. 6). Now all
three of their illustrations represent the oscules as projecting
(pustuliform) and scattered over the frond ; while in Grant’s
illustration of Spongia oculata (Edinb. New Phil. Journ. 1826,
vol. ii. p. 140, pl. u. fig. 22), as well as in Johnston’s Hali-
chondria oculata, they are, as Johnston stated, “‘ mostly
disposed along the margin,” that is on opposite sides of the
cylindrical branch (op. cet. p. 95), which was probably the
case in Esper’s Spongia polychotoma (tab. xxxvi.), as they
are not represented on the surface of the branches of his illus-
tration. Hence it is evident that Esper’s Spongia oculata, so
far as appearance goes, is Johnston’s Halichondria palmata.
But the latter is also stated by Johnston to be the “ Mer-
maid’s Glove’’ of the Shetlanders, which Bowerbank calls
“‘Tsodictya palmata” (Mon. vol. u. p. 311, and vol. i.
pl. lii.), adding very properly to the simple skeletal acerate of
this sponge in his illustration an equianchorate, which, on
microscopic examination, I find to be so peculcar in shape,
that the “ flesh-spicule”’ in this instance becomes a distin-
guishing character, whereby I have been enabled to identify
it with Johnston’s type specimen of his Halichondria palmata
in the British Museum *. Hence also Esper’s Spongia oculata
and Ellis’s Spongia palmata, if they possessed this distin-
guishing character, become Dr. Bowerbank’s “‘sodictya pal-
mata.”
Be this as it may, however, the structure and skeletal
spicule of Johnston’s type specimen of Halichondria palmata
are so like those of Chalina polychotoma that I have not hesi-
tated, in opposition to Dr. Bowerbank’s view, to change his
generic term “‘Halichondria”’ to Chalina palmata, as may be
seen by my description and illustration of the latter in the
‘Annals’ of 1882 (vol. x. p. 109, woodcut, fig. 1), where 1
have fully gone into the subject, therefore need not repeat
any more of it here.
Why Johnston shouid have designated his sponge ‘‘oculata”
after having identified it with Esper’s ‘ polychotoma” I am
* Schmidt’s only instance of this is in the zrequianchorate of his Espe-
ria sentinella (Spong. Kiiste vy. Algier, p. 30, Taf. y. fig. 11).
Sponges from South Australia. 279
unable to conceive, unless he considered that both were only
variations of the same sponge, which I think very likely,
especially as the form of ‘ polychotoma” very often runs into
that of “ oculata ;”’ and Johnston himself, as before noticed,
has placed them together, that is one after the other, in his
‘ British Sponges.’ But then neither “ oculata” nor “ poly-
chotoma”’ possesses a flesh-spicule, which Chalina palmata does,
and Johnston did no¢ know this; so something else must have
influenced him in using this designation, probably the desig-
nation ‘‘ palmata,” which Ellis used for the sponge that
Johnston considered to be his “Halichondria palmata ;”
still, as before stated, unless it could be proved that Hllis’s
sponge contained the peculiarly formed anchorate to which I
have alluded, it is quite as likely, as just stated, that his sponge
was a mere variety in form of Chalina polychotoma.
So much for confusion in nomenclature when names are
based on mere resemblances; but it should be remembered
that all this took place before the achromatic microscope had
been invented, after which distinctions on minute differences
which then came into view were rendered comparatively
easy. We know, however, now that Johnston’s Halichondria
palmata differs in possessing the peculiarly-formed anchorate,
to which I have above alluded, from all the other Chalinida,
and that the species is identical with the “‘ Mermaid’s Glove.”
The chief distinguishing characters of the order RHAPHIDO-
NEMA, in addition to the diagnosis above mentioned, are their
easily yielding to pressure and corresponding resiliency, from
the keratose element of the fibre predominating, the spicular
element more or less scanty, the structure loose, and, as Ellis
noticed in 1786 (op. c7t. p. 185), ‘“ the gelatinous part of the
flesh [the sarcode] is so tender that when it is taken out of the
water it soon dries away.”’ In structure the deeper part is
generally less dense than the circumference, which is also
generally the opposite in the following order, viz. the EcuI-
NONEMA ; hence the former are for the most part easily com-
pressible, while the latter are generally much less so, and
often even absolutely hard. In spiculation there is generally
only one form of spicule, and that is the simple or commonest
form of acerate, viz. smooth, curved, fusiform, and sharp at
both ends; while in the EcHINONEMA there is generally more
than one form, of which one is generally acuate, that is an
acerate with one end obtuse. In the RHAPHIDONEMA the ske-
letal is seldom accompanied by a flesh-spicule, while in the
ECHINONEMA it is seldom without one. The spicule in the
RHAPHIDONEMA is generally confined to the fibre, hence its
280 Mr H. J. Carter on
comparatively smooth surface; while in the ECHINONEMA, as
the name indicates, more or less of the pointed end always
extends beyond it, echinatingly or in tufts. The oscules or
vents are conspicuous in the RHAPHIDONEMA, while in the
EcHINONEMA they are generally inconspicuous, from the
excretory systems in the latter being generally smaller and
thus more numerous, in accordance with their greater density
of structure.
Thus I have contrasted the RHAPHIDONEMA with the
EcHINONEMA because in many instances their forms otherwise
are so much alike; but the structural characters of the Rua-
PHIDONEMA run throughout the order so uninterruptedly that,
different as the forms may be (which have chiefly led to the
grouping), they will be found to be so constant that, although
the order contains a number of species, they may easily be
found out under the arrangement I have made, which, for the
same reason, requires very little revisionary remark.
When I inserted the group “ Palmata,”’ which is the second
on the list, I had not seen Bowerbank’s specimen of the
“¢ Mermaid’s Glove,” now in the British Museum, nor had [
identified it with Johnston’s type specimen of Halichondria
palmata there, by finding that the Jatter possessed the same
peculiar form of anchorate ; so for the present this group can
be considered to be represented by only one species, viz.
Chalina palmata.
There are three other forms, in all of which the skeletal
acerate is accompanied by the same kind of equianchorate
flesh-spicule ; but this is of the common navicular shape, and
all come from the neighbourhood of the Cape of Good Hope,
as will be more particularly noticed hereafter.
Of the groups in the third family, viz. the Acervochalinida,
I can state nothing decisive, excepting that there are solid forms
of RHAPHIDONEMA, but their massive condition, aided only by
the characters afforded by their structure and spiculation, so
far have not enabled me to identify one in particular; while
the ‘ footnote ”’ to the group “ Dictyalia” in my classification
(op. et loc. cit. p. 143), whose purport is as follows, adds still
more to the difficulties, viz. :—“ In some instances the pre-
dominance of the keratine element in the RHAPHIDONEMA is
exchanged for the predominance of the spicular one in the
order HOLORHAPHIDOTA, when the same species must be
placed in one or the other, as the case may be, while the
group ‘Isodictyosa’ in the latter chiefly offers the species
with which those of the RHAPHIDONEMA are most likely to
be confounded.” But such difficulties are inseparable from a
classification made by man to aid his memory, and which
nature ignores !
Sponges from South Australia. 281
Thus, while the facts may be still fresh in the memory of
those who have read my report on the collection of marine
sponges from Japan &c. (‘ Annals,’ 1885, vol. xv. p. 387),
it might be observed that the polychotomous Chalina there
referred to (p. 402), although possessing the same form of
spicule as a similar species from the Mauritius, is a bond fide
solid, branched, and stipitate Chalinoid form characteristic of
my group “ Digitata,” while that from the Mauritius is an
Isodictyal Chalinoid form, in which the skeletal spicule is not
only larger, but accompanied by a minute acerate flesh-spicule.
Hence, while the latter retains the proposed designation, viz.
“ mauritiana,’ the former, for distinction’s sake, might be
designated “japonica.” (This, however, must bejconsidered as
an ex post facto statement, since I was not made aware of the
presence of the flesh-spicule until after I had first written the
passages to which I have referred.)
Now the Mauritius specimen (that Mr. B. W. Priest kindly
submitted for my examination, which, with a true Chalina-
like form, consisted only of a fragment about 3 inches long
and half an inch in diameter), presents on one side a flat sur-
face by which it had adhered toa mass of Nudlipore on which
it had been growing; and thus the sp:cimen bears the same
relation inthis respect to a solid, digitate, erect Chalina of
the British seas, that is C. polychotoma, that the latter does to
our British Halichondria simulans, Johnston (pl. viii.),=
Isodictya simulans, Bk. (Mon. vol. i. pl. li. figs. 5 and 6),
which, although occasionally rising up more or less into a
Chalina-like branched stem, as frequently creeps in this form —
over the surface of the rocks on which it may be growing (see
Johnston’s illustrations, /. ¢.) ; but in the Mauritius specimen,
as before stated, the skeletal is accompanied by a flesh-spicule.
In short the spiculation of the Mauritius specimen consists of
a large sausage-like form with several smaller ones in various
stages of development chiefly about the angles of its reticu-
Jated structure ; and a minute, sharp-pointed, fusiform, acerate
flesh-spicule, chiefly arranged like a row of swallows on a
telegraph-wire, along the course of the large spicule or spicular
reticulation; while also, as before stated, the J apan specimen
only presents one form, viz. the sausage-shaped one, which is
much smaller, as may be seen by my illustrations (‘ Annals,’
l. c. pl. xiv. figs. 12 and 13).
Again, in Dr. Bowerbank’s representations of his Chalina
oculata (Mon. vol. ui. pl. Ixvi.) and that of his “Jsodictya
varians”’ (ib. pl. Ixxxvui.), the former from a specimen from
the open sea in the English Channel off Hastings, and the
latter from one from the mouth or estuary of the Mersey at
282 Mr. H. J. Carter on
Liverpool, close to the entrance of a freshwater tributary, the
only difference that I can see, for I have specimens of both in
my possession, amounts to the simple modification that arises
from a predominance of keratine, whereby the open-sea speci-
men is tougher and more resilient than the estuary one, which,
being the reverse, is softer and more fragile, the spicules
being much the same in size and shape in both.
How far the general form and the sausage-shaped spicule
of the freshwater sponge Uruquaya corallioides, Bk., which
equally agrees in these respects with both Chalina japonica
and Chalina mauritiana, may favour the view of those who
would refer Uruguaya to a marine origin, | am not able to say ;
or to come to the conclusion of Dr. W. Dybowski that, because
Lubomirskia batcalensis, viz. the solid, caulescent, branched,
chaliniform freshwater sponge of Lake Baikal, in Central
Asia, is identical in general structure and in the form and
nature of its spicule with a similar but marine one which his
brother sent him from the shores of Behring’s Island, in the
Kamtschatka Sea,—the former is necessarily the latter living
in fresh water (“ Die Behringsschwimme weichen weder in
ihrer Struktur noch in der Gestalt und Beschaffenheit der
Spiculen von denen der Baikalschen Exemplare ab, so dass alle
diese, obgleich aus so sehr verschiedenen Fundorten herkom-
menden Schwimme, als vollkommen identisch anzusehen
sind,’ Sitzungsbericht d. Dorpater Naturforscher-Gesell-
schaft, Jahrg. 1884, p. 45), although geologically considered
it is as easy to infer that the sea, when receding from the
interior of continents, might have left saltwater lakes there,
which have become as fresh as the marine formations beside
them, in which there is now not a particle of salt left. But
as yet, if neither Uruguaya nor Lubomirskia baicalensis has
been found to possess statoblasts, so neither have they been
found in an ovigerous condition—conditions, especially of
the latter, which can only be maintained for home-demonstra-
tion by being at once preserved in some aqueous medium,
such as spirit and water ; ¢. e. on the spot.
I have entered more at length into this subject here than
I had an opportunity of doing in my report on the Japan
sponges, chiefly because the Mauritius sponge is, according
to my view, a Chalina (C. mauritiana), and its spiculation
so peculiar that it is deserving of special mention.
Lastly, for my observations on the fourth or concluding
family of the order RHAPHIDONEMA, viz. the Pseudochalinida,
I must refer the reader to the species described in the ‘ Annals’
of 1882 (vol. ix. p. 280), and 1885 (vol. xv. p. 319).
Sponges from South Australia. 283
Returning to the first family, viz. the Chalinida, it might
be observed that this was, as before noticed, the name given
by Dr. Grant to the third order of his Portrera (Tab. View
An. Kingdom, 1861, p. 76, Walton and Maberly) for the
purpose of including sponges ‘ possessing the structure of
Johnston’s Halichondria oculata,” which is our Chalina poly-
chotoma =Spongia polychotoma, Hsper, =Chalina oculata,
Bk.; and it may also be observed in the “ Key to my Clas-
sification of the Spongida”’ (Op. et loc. cit. p. 193) that I
have given this as the type of group No. 1, viz. the “ Digi-
tata,” whose “typical structure,’ to which I have before
alluded only in a general way, may be more particularly
stated as follows:—‘‘ A stipitate bunch of caulescent cylin-
drical stalks, more or less ramosely dividing dichotomously
and polychotomously, more or less interuniting on their way
to their termination in rounded ends.. Easily yielding to
pressure, but still very resilient. Colour, when dry, light
sponge-yellow, often retaining traces of purple, which appears
to be its original colour, at all events in many instances.
Surface uniformly smooth, which is not the case in the ECHINO-
NEMA. Vents chiefly in single lines, opposite to each other,
on each side of the cylindrical stalk. Structure internally
open, where the sarcode, which is very thin (as Ellis noticed),
has disappeared, as is usually the case in dried specimens ;
more compact towards the surface, where the dermal struc-
ture is finer and closer than that which is below it. Fibre
predominantly keratose; spicule acerate, curved, fusiform,
smooth, sharp-pointed, variable in size, which is chiefly small,
often minute. General form also variable.”
As regards the latter character, viz. the variability in form,
IT cannot do better than refer the reader to Miklucho-Mac-
lay’s paper (Mém. de l|’Acad. de St. Pétersb. vii. s. t. xv.
no. 3, 1870) on the varieties of his “ Veluspa polymorpha,”
which is an estuary specimen of Chalina polymorpha, as may
be seen by reference to the typical form (Taf. 1. fig. 1), among
which the Baikal freshwater sponge Lubomirskia bathalensis,
Pallas, is introduced as No, 11 (Taf. i. fig. 5).
This brings us to the consideration of the specimens of
RHAPHIDONEMA in Mr. Wilson’s collection from the neigh-
bourhood of Port Phillip Heads, Victoria Col., S. Australia,
which, although very numerous, belong to only three groups :
viz. the Digitata, the Tubulodigitata, and the Bivalvata
respectively, but mostly to the first, under which Chalina
polychotoma and its varieties will presently be mentioned, fol-
lowed by a single species of Tubulodigitata and the same of
284 Mr. H. J. Carter on
Bivalvata. In all the spicule is of the same form, viz. acerate,
smooth, curved, fusiform, and sharp-pointed, but for the most
part very small and often minute, 7. e. not exceeding 7-6000ths
in. in length, with almost immeasurable thinness, combined
with great thickness of keratine in the fibre, which, as before
stated, leads to great toughness and resilieucy. In my British
specimens of Chalina polychotoma, obtained from the English
Channel opposite this place (Budleigh-Salterton), the spicule
is about 30 by 24-6000ths inch in its greatest dimensions.
Fam. 1. Chalinida.
“‘ Ohar. Digitations solid, vertical or procumbent.”
Group 1. DIGITATA.
Chalina polychotoma, Esper.
Of this species in Mr. Wilson’s collection there are several
specimens, whose characters having already been mentioned,
need not be repeated here. Largest specimen 2 feet long,
Depth not mentioned. Neither the colour when fresh nor the
depth of the dried specimens is stated.
Chalina polychotoma, var. trichotoma.
Described in the ‘Annals’ for 1885 (vol. xv. p. 115).
This variety only differs from the foregoing in most of the
ends of the branches being more or less expanded and tricho-
tomously divided. 19 inches long. Presented to the British
Museum in the name of J. Bracebridge Wilson, Esq., M.A.,
F.L.8. Dried specimen.
Chalina polychotoma, var. compressa.
Where the stem becomes more or less expanded and com-
pressed at the commencement of the branches, or where the
latter becomes expanded towards their ends spatuliform (spa-
tulata). Vents scattered over the expanded portions, chiefly
on one side, comparatively small and not projected. Two
wet specimens :—viz. 1, wholly compressed ; colour, when
fresh, “ purple-slate ;”? 52 in. long. 2, subcompressed ;
colour, when fresh, ‘ pale buff-brown ;”’ 13 in. long. Depth
of both 19 fath.
Chalina polychotoma, var. oculata.
Stems thick, more or less irregular in form, 7. e. more or
less irregularly expanded and united together in their whole
length, flabelliform, proliferous. Colour dark-brown reddish.
Sponges from South Australia. 285
Surface smooth. Vents large, circular, projected pustuliformly,
scattered over the surface generally, or, where the branch is
expanded, chiefly on one side.
Obs. Here I should be inclined to place Esper’s Spongta
oculata (tab. i.) and Ellis’s Spongia palmata (tab. lviii.
fig. 6), if, as before stated, they were not possessed of the
peculiar anchorate of Chalina palmata, Johnston.
Chalina polychotoma, var. robusta.
In which the stems are few, thick, and large, with smallish
vents on one side chiefly. Wet specimen. Colour, when
fresh, “ orange-buff.”” 11 in. long.
Depth 20 fath.
Chalina polychotoma, var. angulata.
Stem nodosely angulated, zigzag instead of being uni-
formly cylindrical ; presenting a knotted appearance, in which
the nodose portion may be slightly prolonged branch-like on
each side, so as to give the stem an alternately jointed zigzag
aspect. Colour dark black-brown on the surtace, light brown
interiorly, or light brown throughout. Surface soft, velvety
from the fineness and compactness of the dermal tissue. Vents
of two sizes, large and small, scattered over the nodose por-
tions irregularly. Fibre and structure finer and more compact
than in C. polychotoma, accompanied by more remains of the
sarcode. Size of largest specimen, which is wet, 15 in. long.
Colour, when fresh, not given.
Depth 19 fath.
Chalina polychotoma, var. moniliformis.
Stems successively inflated more or less regularly. Colour
light brown. Surface velvety. Vents scattered over the
bullate inflations. ‘Texture, ¢.e. the fibre and structure, as
in the foregoing variety, viz. “ angulata.”
Obs. 'This comes in as a sequence of very common occur-
rence, but not represented in Mr. Wilson’s collection, although
there are several large specimens in the British Museum
which come from the south coast of Australia.
I have briefly enumerated these varieties in form, not only
because they are chiefly present in Mr. Wilson’s collection, but
still more because they are of general occurrence: that is, the
stalks, originally smooth and cylindrical in the typical form, viz.
Chalina polychotoma, may become partially flattened; then
expanded and more or less united laterally either at the com
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 20 |
286 Mr. H. J. Carter on
mencement or at the extremities ; then expanded and united
generally into a flahellate more or less proliferous plane ;
lastly, jagged or irregularly moniliform ; while the vents may
be comparatively small and linearly arranged opposite to each
other on the cylindrical branch in the typical species, scattered
in the compressed forms, and projected pustulitormly in
the oculate specimens. The colour may vary from light
sponge-yellow to dark sponge-brown, more or less mixed with
red, and often to reddish purple ; but, of course, this is useless
for specific distinction.
Fam. 3. Cavochalinida.
‘Tubular, vasiform, aculeated, patulous or compressed
flabellately ; plane and frondose or dactyloid.”
Group 8. TUBULODIGITATA.
Patuloscula procumbens, Carter (‘ Annals,’ 1882, vol. ix.
; p- 365).
Short, thick, thumb-shaped, cylindrical, bullate, hollow,
erect processes, growing side by side on a common expanded
base, spreading in a branched form horizontally. Consistence
resilient. Colour, when fresh, ‘ purple-slate,’’ now sponge-
yellow brown. Vent terminal, cloacal, circular at the end of
the process, contracted, but still enormously large. Spicule
acerate, as before. Size of specimens, of which there are two,
varying from 2 to 6 in. high, and 6 x 4 horizontally.
Depth 7 to 14 fath.
Obs. This is also a West-Indian sponge and appears to
have been noticed and illustrated by De Fonbressin and
Michelotti under the name of ‘“ Callyspongia bullata”
(‘ Spongiaires de la mer Caraibe,’ Harlem, 1864, p. 56, pl. x.
fig. 5). I have already given the name to some beautiful
specimens of it, bronght home from the West Indies by the
Rev. H. H. Higgins, now in the Liverpool Museum, in one
of which the bullate processes, successively inflated, are ex-
tended upwards separately for 3 or 4 inches. A specimen of
these was also presented to the British Museum in the month
of March 1877. It is not the Spongia bullata of Lamarck
= Sp. tubulosa, Esper, tab. 54, since the vents here are czliated,
as 1). et M. have noticed, which allies it to their genus.
“ Tuha,” that is typical of our groups Aculeata &e. (see
my ‘Classification,’ /. c. ‘“ Key,” p. 194; and for the
genns “ Tuba,” generally, ‘ Annals,’ 1882, vol. ix. p. 277
et sev, West Indian and Acapulco sponges).
Patuloscula procumbens, var. flabelliformis.
In this variety the successively dilated bullate tubes or
Sponges from South Australia. 287
processes, which are very long comparatively, are united
laterally throughout into a fan-shaped form, rising from a
single stem, the large circular vents being arranged serially
on the margin. Largest specimen about 8 in. high by 8x 1
in. horizontally. Colour, when fresh, “ buff-grey.”
Depth 20 fath.
Group 9. BIVALVATA.
Cavochalina bilamellata, Lam.
Stipitate, placentiform, doubled up like a bivalved shell
with a stem, ¢. e. vasiform compressed ; infundibular below
as the head approaches the stem, which is long and hard,
ending in a root-like expansion, expanding, in the contrary
direction, into a flabelliform bilamellar head above. Con-
sistence leathery. Colour, when fresh, “ pale pinkish brown,”
now mouse-brown. Surface externally wrinkled, rugosely
reticulated in high relief, nodose; inside even, smooth, con-
centrically lmeated. Vents small, scattered over the inner
surface. Structure compact, fine, composed of short-jointed
keratose fibre, scantily charged with the usual form of small
spicule, viz. acerate, smooth, curved, fusiform, sharp-pointed,
about 14 by 2-6000ths in. in its greatest dimensions. Size
very variable, apparently increasing with the age of the
specimen ; the largest, of which there are several dry, but only
one wet specimen, about a foot each way, including the stem,
which may be 3 or 4 in. long, with a thickness of the head
tewards the stem about one inch where the nodular excrescences
are most prominent, becoming gradually thinner in the oppo-
site direction, that is towards the border, where the nodular
processes ceasing leave a narrow smooth strip about one
sixth of an inch in thickness.
Depth 19 fath.
Hab. Marine.
Loc. Port Phillip Heads, south coast of Australia.
Obs. This seems to me to be the species briefly described
by Lamarck (1st ed. t. 11. p. 866, no. 61), so I have given
it his designation. ‘There are several dry specimens in Mr.
Wilson’s collection, but only one wet one. From the great
number which | have seen it must be very plentiful under all
torms on the south coast of Australia, but all modifications of
that above mentioned ; whilst its leathery imperishable nature
and great toughness arising from the quantity of keratine in
the composition of its fibre, scanty and small spiculation, and
compact structure, render it as durable almost as the sole of
ashoe. It is subject to considerable variety in form, being
20*
288 Mr. H. J. Carter on
sometimes expanded horizontally and proliferously foliated or
cabbage-like.
Group 11. PLICATA.
Although not in Mr. Wilson’s collection, but coming from
hard by, viz. the neighbourhood of the Cape of Good Hope,
and therefore probably represented on the south coast of
Australia, I would here insert the following description of the
specimen, which is intended to typically illustrate the species
for which this group was instituted, as although promised in
my Classification, it has not hitherto been given.
Textiliforma foliata.
Large mass of cloth-like, flat, very thin and expanded fron-
dose portions, rising from a contracted short stem, apparently
independent of each other, but, in fact, all continuous, although
so interfolded and deeply indented at the margin as to present
a plurality of separate dissepiments; or, in a large, single,
semicircular, stipitate, frondose form, more or less proliferous.
Consistence firm, resilient. Colour, now in its dried state, pale
yellow-brown, with traces of the original sarcode, which was
purple. Surface uniformly even on both sides. Vents, in
little groups, petaloid, rosette-like, scattered plentifully over
the surface; each group about 1-24th in. in diameter and
1-12th in. apart ; but while confined to one surface only this
depends upon the position of the fold, so that on one part they
may be on one side and on the other on the other ; hence they
are in patches, that is not continuous throughout the same side
of the frond, in the interfolded or plicate form; while, of
course, in the other form, where there is no plication, they are
allon one side. Internal structure compact, tough, formed of
short-jointed keratose fibre charged with the usual form of
acerate spicule internally, and surrounded by sarcode equally
charged with the same spicule together with a number of
equianchorates or flesh-spicules. Skeletal spicule curved,
smooth, fusiform, sharp-pointed, about 28- by 25-6000ths in.
in its greatest dimensions. F'lesh-spicule, a navicular shaped
equianchorate with rather obtuse ends when viewed in front,
about 6-6000ths in. long. Size of largest specimen 17 in.
high by 12 in. broad; wall of the frond or lamina ¢ in. thick.
Hab. Marine.
Loc. Cape of Good Hope and its neighbourhood.
Obs. There are several specimens of this sponge in the
British Museum (all dry, of course), viz. No. 60, registered
71. 5. 12. 1, &c. from Port Elizabeth; and No. 509, regis-
tered 40. 9. 28. 27, from “ the Cape ;” together with two other
Sponges from South Australia. 289
forms from “the Cape,” presenting a similar structure and
spiculation, viz. Chalina compressa, which has already been
described in the ‘Annals’ of 1882 (vol. x. p. 112), and
might be relegated to the group “ Palmata” for the present,
as representing the “ Mermaid’s glove” at the Cape; and a
third, which from its form might be relegated to the “ Digi-
tata’”” and termed “ Chalina polychotoma, var. anchorata,”
as its skeletal acerate is also accompanied by an equianchorate
flesh-spicule ; but in the two latter the navicular anchorate is
pointed at the ends instead of being round or obtuse; although
_ in all three instances belonging to that kind which from its
boat- or shuttle-like shape I have termed navicular.
These are the specimens from the ‘ neighbourhood of the
Cape of Good Hope” to which I have alluded, at p. 280, as
possessing the same kind of naviculiform anchorate.
Ovigerous Specimens.
In the ovigerous specimens, of which there are a great
many in Mr. Wilson’s collection, not only of the RHaPHrbo-
NEMA, but of all the other orders, the form and position of the
ova remain; but the same astringent effect of the spirit which
has kept them thus has contracted their contents into a cheesy
consistence which defies all attempt at further elucidation.
In short, to do anything with the soft parts of a sponge in the
microscopical or more minute way it is absolutely necessary to
examine them immediately after they have been taken from
their native habitats, that is while they are living. Much
may be done by putting them into spirit and water at once
and examining them a few days after they have been thus
preserved; but the longer they remain after this the more
these parts become chemically altered by the methylated
spirit and rendered unfit for anything but a display of the
larger parts of which they are composed, from the change
especially in the contents of the ova and the sperm-cells, to
which I have above alluded; and the development of calca-
reous crystallizations in the general tissue. :
Order V. ECHINONEMA.
For the reasons above mentioned I shall also insert here a
tabular view of my arrangement of this order in 1875 (op. et
loc. cit.), VIZ. :—
290 Mr. H. J. Carter on
Families. Groups.
1. Pluriformia.
2. Plumohalichondrina.
3
lle VOR? a sncouconesepeoand 4 3. Microcionina.
| 4. Kchinoclathrata.
5. Baculifera.
AN 6. Multiformia.
Ph We GREGG GS Ines ats RAR DOG 6 eS 17 Disa
And here I would observe that this order is by far the most
difficult of any that I have had to contend with; not so much _
probably in the first family, viz. the Ectyonida, as in the
second, viz. the Axinellida; hence in both they are headed
with a group provisionally named, which has thus been
indefinitely given for the purpose of enabling the spongiolo-
gist to supply its place with a plurality of groups that of
course must vary in amount, name, and description as more
extended observation may dictate, which, judging from the
enormous number of species and varieties from all parts of the
world, represented by the dried and beach-specimens in the
collection of the British Museum, almost tempts one to
exclaim, ‘‘ Where is this to end ?”’ and as one species so often
resembles another in one or more points, to ask ‘ What cha-
racter is there in one species which is not to be found in
another?”’ But probably similar observations were made at
the commencement of the study of conchology&c. ; still it seems
to me certain that, as in other branches of natural history, the
class, orders, and families may be restricted to a few simple
characters for leading to the groups and genera, but nothing but
a combination of characters will lead the student to the species,
which is the great thing after all, and those it is desirable, for
practical purposes, to limit as much as possible to what can be
seen with the commonest microscope, otherwise the distinc-
tions become one for the rich man only who has plenty of
leisure and can easily afford to purchase a fine instrument ;
which, of course, is also desirable; but then this cannot be
for the many, but for the scientific, or, as it may be termed,
esoteric few. Hence “ equality” is as utopian, as imequality
is absolutely necessary for progress in all human affairs.
Such knowledge can only come to the poor through the rich.
The diagnosis of the order KCHINONEMA, viz. :—‘“‘ Possess-
ing a skeleton composed of horny fibre cored with proper
spicules internally and echinated with proper spicules exter-
nally. Form ot spicules chiefly acuate,” so far as the first
family, viz. the Ectyonida, goes, cannot be more practically
Sponges from South Australia. 291
useful, for I know of no exception toit. But it does not apply
so satisfactorily to the second family, viz. the Axinellida ;
neither does the special diagnosis of this family, viz. :—
“‘ Hchinated with proper spicules projecting from the ¢nterior of
the fibre,” suffice for all, since it may be the case to a certain
extent with species of the RHAPHIDONEMA; but by adding
the words :—‘“‘ Structure increasing in density ¢mwards or
towards the first-formed parts, that is the axis,” which for the
most part is a peculiarity common to the whole order, although
not needed in the diagnosis of the first family, that of the second
family is rendered almost equally useful.
It will be observed by referring to the above “ table” that
each of the families commences with a “ group,” whose name
etymologically has the same signification, viz. “ Pluriformia”’
and “ Multiformia,” which, as before stated, were provisionally
instituted, because the specimens which appeared to belong
to them respectively were at the time of classification so
numerous as to be quite overwhelming ; therefore all that I
could do under the circumstances, that is with little or no
literature for my guidance, was to keep them together, as I
have before observed of the Psammonemata, under the
families mentioned, for subsequent division into groups when
their species, by individual description from undried and
entire specimens, should be typically determined. It was
this to which my dear old friend Dr. J. HE. Gray alluded
when he said :—‘‘ The greatest contributor to our knowledge
and advancement of spongiology in its present state will be
he who correctly describes and illustrates most species.”
Fam. 1. Ectyonida.
Group 1. PLURIFORMIA.
In the “key” to my classification (/. c. p. 195) I have
given the names of several kinds of sponges which I then
thought might become types of the subdivisions of this group,
and during the last ten years which have elapsed since that
was published I have occasionally been able to substantiate it
thus:—‘‘Ectyon sparsus”’ has led to the formation of the
group ‘ Eetyonina”’ or “ Eetyones” (‘ Annals,’ 1883, vol.
xi. p. 310, &e.) ; “Hehinonema typicum” to one for which I
would propose the name of “ Echinonematina” (cd. 1881,
vol. vil. p. 378, &c.) ; “Dictyocylindrus ramosus, Bk.,” &e.
to that of ‘ Dictyocylindrina ” (7b. 1879, vol. iii. p. 295) ; and
“Spongia muricata, Pallas,= Trikentrion muricatum, Ehlers,”
293 Mr. H. J. Carter on
to that of the group “ Trichentrionina” (2b. 1879, vol. ill.
p- 293, &e.).
Groups 2, 3, and 4 of the Ectyonida, viz. Plumohalichon-
drina, Microcionina, and Hchinoclathrata, I must leave as the y
are, merely observing that “‘Halichondria servata,” Johnston ,
= Ophlitospongia (olim Chalina) seriata, Bk., unfortunately
does not illustrate the group etymologically, on account of
being solid instead of clathrate ; but then it was, as it is now,
the only species of the group that had been publicly de-
scribed, so that I had no option, but will now endeavour to
supply this apparent discrepancy by adding the description of
a dried foreign species, equally remarkable for its clathrate
character, which is solidly cellular throughout rather than
simply solid, and thus resembles the nidamental mass of a
whelk or a bee’s honeycomb rather than a sponge :—
Lchinoclathria favus, n. sp.
Massive, lobed, sessile or contracted towards the base, or
divided digitately from this upwards into a bunch of coales-
cent cylindrical stems, dichotomously and polychotomously
branched, like a digitate Chalina. Consistence now in its
dried state soft and resilient. Colour reddish brown or
yellowish. Surface even. Structure composed of a thin
fibro-reticulate lamina, continuous in itself, but partitionally
separating vermicular cavities, which are equally continuous
throughout, thus producing a uniformly clathrous mass which,
on the surface, presents a honeycomb appearance, in which
the cells, which are irregular in outline, are about 3-12ths
in. in diameter more or less. Fibre both cored and echinated
with proper spicules. Core- or skeletal spicule very thin,
subpin-like, smooth, fusitorm, constricted towards the head,
about 45-6000ths in. long. Hchinating spicule smooth, also
subpin-like, fusiform, and constricted towards the head, which
is less in diameter than the shaft, about 15 by 14-600Uths in.
in its greatest dimensions. Size of specimens variable.
Hab. Marine.
Loe. South coast of Australia.
Obs. This sponge is so striking in its honeycomb algoid
appearance and soft though resilient consistence that it can
hardly be mistaken for any other excepting the areniferous
variety of the same sponge, which will be described hereafter
in the new family which I propose to eall “ Pseudoechino-
nemida.”’
There are several specimens of it in the British Museum,
mostly under 4 inches in their greatest diameter, of which
nos, 054 and 505, each registered 59. 10. 7. 106, may be
Sponges from South Australia. 293
mentioned as massive forms, and no. “ 208 dis,” registered
37. 5. 13. 36 &c., as more or less digitate forms somewhat like
those of Chalina polychotoma ; so that it appears to be by no
means common, although it is so remarkable in structure.
Again, in group 5, viz. the Baculifera, the echinating
spicule is not spined, but its hammer-shaped or crutch-like
head is imbedded in the surface of the fibre, together with a
like form in its interior, which, combined with its cork-like
consistence, unmistakably defines this type.
HIGGINSINA, new group.
Lastly, to this family I must add the group above men-
tioned, viz. ‘‘ Higginsina,” for sponges in which the apparent
analogue of the spined echinating spicule is not club-shaped,
but acerate, that is fusiform and sharp-pointed, and no¢ echi-
nating, but /oose in the tissue ; for a typical species of which
I must refer the reader to the West- Indian sponge ‘‘Higginsia
coralloides”’ and its varieties described and illustrated by
Mr. Thomas H. Higgin, F.L.8., in the ‘ Annals’ for 1877
(vol. xix. p. 291 &c. pl. xiv. figs. 1-5). Called after the Rev.
H. H. Higgins.
To this I will add the following description of a Cape
variety of this sponge, in which the wnattached position of
the echinating spicule is not so evident, and an acuate is
added to the acerate skeletal spicule.
Higginsia coralloides, var. natalensis, n. var.
Flabelliform, erect, stipitate, ridged on each side prolife-
rously ; ridges thin, ragged, and in strong relief, radiating
and branching from the stem to the circumference. Consis-
tence tough, firm, in the dry state, with hard inspissated sarcode
and compact structure. Colour orange. Surface uneven,
hispid. Spicules of three forms, viz.:—1, skeletal, thick,
smooth acuate, 70 by 3-1800ths in. in its greatest dimensions ;
2, subskeletal, thin, smooth acerate, about 50 by $-1800ths
in.; 3, echinating spicule, a spinous acerate rather bent than
curved in the centre, about 8 by 3-1800th; no. 1 is arranged
in tufts surrounded by no. 2 in great numbers, among which
is no. 3, all projecting outwardly, as they successively and
together emanate from the fibre. Size variable, the largest
specimen 54 in. broad by 23 in. high.
Hab. Marine.
Loc. Port Elizabeth, Cape of Good Hope.
Obs, Of this species, whose spiculation is somewhat diffe-
294 Mr. G. A. Boulenger on
rent, although evidently belonging to the genus Aigginsia
in other respects, there are several dry specimens in the
British Museum, of which No. 18 is the largest. No. 40 is
an elkhorn-shaped, rat-tailed, flat, branched variety, and Nos.
16,17, and 19, all more or less like that above described,
and all registered 71. 5. 12. 1 &c.
Gen. obs. In many of the Ectyonida there are flesh-
spicules, viz. equianchorates, bihamates, or tricurvates, and
these may be alone or combined. ‘The anchorate is generally
of that kind termed navicular from its boat-like form, @. e. sharp
at each end ; the bihamate a small simple C- or S-shaped one ;
and the tricurvate also small and simple. In one instance,
however, the anchorate is “angulate,” that is, the shaft is
bow-shaped and turned up at the ends (see Bowerbank’s
illustration, Mon. Brit. Spong. vol. 1. pl. vi. fig. 143), cha-
racterizing the Plumohalichondrina; but in the rest the
flesh-spicules do not seem to be of much specific value, on
account of the sameness of their form. One more observation
I would add here, viz. that the curve of the acuate skeletal
spicule in the ECHINONEMA is so generally on one side the
middle, and towards the obtuse end, that when I see this I
feel almost confident that the sponge from which it came
belongs to this order.
[To be continued. |
XXVIII.—Remarks on a Paper by Prof. E. D. Cope on the
Reptiles of the Province Rio Grande do Sul, Brazil. By
G. A. BOULENGER.
Pror. Copr’s “ Twelfth Contribution to the Herpetology
of Tropical America’’*, contains a list of Reptiles and
Batrachians from the Province Rio Grande do Sul, collected
by the “ Naturalist Brazilian Exploring Expedition.” Having
lately been engaged in naming large series of specimens from
the same country, transmitted to the Natural-History Museum
by the zealous Dr. H. von Ihering, and which have afforded
material for several contributions published in these ‘ Annals’ +,
I am able to present a few critical remarks on Prof. Cope’s
identifications and new species. Besides, the nomenclature
adopted by the American herpetologist differs im so many
* Proc. Amer. Phil. Soc. xxii. pp. 167-194 ; April 1886.
+ March, April, and August numbers, 1885.
Reptiles from Brazil. 295
points from that followed by me, that it will be useful to
place side by side the names used by us. The following is
the list of the species as enumerated by Cope, with the names
used in my previous “ Lists.’” Species not contained in my
Lists are preceded by an asterisk.
REPTILIA.
LACERTILIA.
Corr. BoULENGER.
1. Anops Kingii, Bell. = Anops Kingii.
2. Amphisbzena trachura, Cope, = Amphisbeena Darwinii.
sp. 2.
3. Aporarchus prunicolor, Cope, = Amphisbzena Darwinii.
g. and sp. n.
4, Pantodactylus bivittatus, = Pantodactylus Schreibersii,
Cope. Wiegm.
5. Acrantus viridis, Merr. = Teius teyou, Daud.
6. Tejus teguexin, L. = Tupinambis teguixin.
7. Opheodes striatus, Wagl. = Ophiodes striatus.
OPHIDIA.
8. Phalotris melanopleurus, = LElapomorphus lemniscatus, D.
Cope, sp. 0. r B.
9. Opheomorphus dorsalis, = Liophis Jaegeri, Gthr.
Ptrs.
10. fuscus, Cope, sp. n. = cobella, L.
qa: meleagris, Shaw. = Merremii, Wired.
12. Aporophis conirostris, Gthr. = almadensis, Wagl.
13. cyanopleurus, Cope, = Dromicus melanostigma, Wag.
sp. 1.
*14, Tachymenishypoconia, Cope.
15. Thamnodynastes Nattereri, = Thamnodynastes Nattereri.
Mik.
*16, Drymobius pantherinus,
Merr.
17. Herpetodryas carinatus, Z. = Herpetodryas carinatus,
18. Philodryas Schottii, vz. = Philodryas Schottii.
*19, Olfersii, Fritz.
20. Tropidodryas estivus, D. = eestivus.
B.
#21, Leptognathus Catesbyi, D.
& B.
22. Oxyrhopus rhombifer, D. = Oxyrhopus petalarius, Z.
B.
#23. plumbeus, zed.
24, Lystrophis d’Orbignyi, D. = MHeterodon d’Orbignyi.
B.
*25, Xenodon rhabdocephalus,
Boie.
*26, Neovidii, Gthr.
296 Mr. G. A. Boulenger on
CopE. BovuLENGER.
27. Helicops infrateeniatus, Jan.
28. baliogaster, Cope, sp. un.
29. Elaps altirostris, Cope.
30. Bothrops alternatus, D. § B.
Helicops carinicaudus, Wied.
carinicaudus.
Elaps lemniscatus, LZ.
Bothrops alternatus.
Neil tl fl
BATRACHIA.
31. Bufo @Orbignyi, D.§ B. = Bufo dOrbignyi.
32. marinus, Z. = marinus.
33. Engystoma ovale, Schn. = Engystoma ovale, var. bicolor.
34. Hyla Vauterii, D. § B. = Hyla pulchella.
35. pulchella, D. & B. = pulchella.
36. Paludicola ranina, Cope, Paludicola gracilis, Bigr.
sp. nD.
37. Leptodactylus ocellatus, LZ.
38. ——- mystacinus, Burm.
39. Pseudis paradoxa, Laur.
Leptodactylus ocellatus.
mystacinus.
Pseudis mantidactyla, Cope ?
Observations on the above Identifications.
2, 3.—That the two new species, Amphisbena trachura and
Aporarchus prunicolor, the latter the type of a new genus, are
identical with A. Darwinit I can affirm. The principal
character upon which the former is founded, viz. the ‘ several
terminal rings of the tail very distinct and divided into promi-
nent hard tubercles,” is merely an individual anomaly. A
species has already been made on a somewhat similar peculi-
arity (A. heterozonata, Burm.), but has been justly referred to
the synonymy of A. Darwinit by Strauch, who has examined
the type specimens. The new genus Aporarchus “is simply
Amphisbena without preanal pores.” A. prunicolor is nothing
but a young specimen in which the pores are undistinguishable
(or absent), as I have myself observed among the numerous
specimens of A. Darwinii which have lately passed through
my hands. Strauch also mentions a specimen of an Amphis-
benoid (Anops Kingii) abnormally destitute of preanal pores.
8.—Very curiously a colour variety of Hlapomorphus
lemniscatus has been described three times within two
months :—by Strauch as Hlapomorphus Iheringit, sp. n.; by
myself as a variety of EH. lemniscatus; and by Cope as Pha-
lotris melanopleurus, sp.u. I have already shown that the
characters given by Strauch do not even justify a subspecitic
distinction. This is further confirmed by Cope’s description ;
while Strauch gives as unique structural character of his new
species, as compared with H. lemniscatus, a very broad snout,
Cope describes the snout as narrow; and he also remarks
Reptiles from Brazil. 297
that one of his specimens presents a black vertebral line which
is absent in the others, the only remaining character upon
which both descriptions agree being the continuous black
colour of the lower and lateral surfaces. Since my remarks
on the variations of this snake were written, the Natural-
History Museum has received a ninth specimen, collected by
Dr. v. Ihering at §. Lorenzo. ‘This is larger than any
hitherto recorded, measuring 700 millim. ; snout very broad ;
coloration typical ; ventrals 207, anal divided, caudals 23.
10.—T wo closely allied species of Liophis occur abundantly
in the province Rio Grande do Sul, one with nineteen rows of
scales, the other with seventeen. ‘The former was referred
by me to L. Merremit, auct. (C. meleagris, Shaw), a view
also taken by Cope. ‘The second species I put down as L.
cobella, to which it comes nearest, and of which an identical
specimen was already so named in the Natural-History
Museum ; this is the form now named Opheomorphus fuscus.
Whether it really deserves to rank as a species or ought to
be regarded as a race of L. cobella is adoubtful question. At
any rate it is a distinct form, characterized by the coloration
and a somewhat greater number of ventral shields. Cope
counts 182 ventrals, but this must be an extreme; the nine
specimens before me give the following numbers :—165, 166,
167, 168, 170, 170, 172, 174, 175. In a dozen specimens of
the typical Z. cobella I find the number of ventrals varies
from 143 to 161.
13.—After careful comparison of the description of Apo-
rophis cyanopleurus with the specimens identified by me as
Dromicus melanostiqgma, Wagl., as well as with the figure of
the type specimen published by Jan, I have no doubt the two
forms are identical.
27, 28.—The two species of Helicops mentioned by Cope
are identical, and I have at present before me specimens of
both, as well as of H. carinicaudus, of which I regard them
as varieties. Cope himself, it is true, remarks of his HZ. balio-
gaster that ‘this species is near the H. infrateniatus, Jan,
and future investigation may prove it to be a variety of that
SUOCIGS: 2 2g The colour of the lower surface in the two
species is quite different.” [can assure him that the latter
difference does not even indicate a constant variety, as one of
Dr. v. Ihering’s specimens represents the typical . infra-
teniatus on the anterior half of the ventral surface and the
H. baliogaster on the posterior.
298 Mr. A. G. Butler on Lepidoptera from
35, 36.—A number of specimens of Hyla pulchella obtained
by Dr. v. Ihering have convinced me that the difference in
the dentition upon which H. Vauterti has been separated
from that species is merely individual, and I therefore unite
the two.
37.—The description of Paludicola ranina agrees with my
P. gracilis, published in January 1883, but which Prof. Cope
appears to have overlooked.
40.—The occurrence so far south of Pseudis paradoxa
would be surprising ; but as the list does not mention P. man-
tidactyla, which is very abundant in the province, I cannot
help suggesting that an error in the determination has been
made.
In conclusion, I think not one of the new species described
in Prof. Cope’s paper deserves to stand, with the exception,
perhaps, of Liophis fuscus. His list contains only seven
species not recorded in mine ; of these, four have already been
mentioned from Rio Grande do Sul by Hensel, viz. :—Dry-
mobius pantherinus, Philodryas Olfersii, Xenodon rhabdo-
cephalus, and X. Neovidui. Tachymenis hypoconia, Lepto-
gnathus Catesbyi, and Oxyrhopus plumbeus are apparently
recorded from that province for the first time.
XXIX.—On a Oollection of Lepidoptera made at Manipur and
on the Borders of Assam by Dr. George Watt. By ARTHUR
G. Butter, F.L.8., F.Z.8., &e.
[Plate VIII. ]
In the year 1880 I had the pleasure of bringing before the
Zoological Society an account of a collection made by Dr.
Watt (Professor of Botany in the Calcutta University) prin-
cipally in North-west India, and containing eight new species.
Shortly after the publication of this paper Dr. Watt returned
to India with the intention of starting immediately to explore
Manipur; I, however, heard nothing more of him until the
autumn of 1883, when he forwarded a large box of Lepido-
ptera in envelopes, and amongst them a smaller box of
mounted specimens of all the species taken in Manipur, the
remainder of the species having been obtained “ on the N.E.
frontier of India bordering on Assam.”
Manipur and the Borders of Assam. 299
Thirty-five species were obtained at or on the approach to
Manipur, of which the following is a list :—
Caduga melaneus, Cr. Appias eleonora, B.
Ypthima nareda, Koll. vacans, Bil.
Thaumantis diores, Dbl. Hiposcritia lalage, Gir.
camadeva, Westw. pseudolalage, M.
Moduza procris, Cr. argyridina, Bti.
Athyma cama, M. shiva, Swen.
Rahinda hordonia, S¢. mahana, MZ.
Kuthalia teuta, Dov. Huphina nama, M.
Sympheedra dirtea, F. Ganoris gliciria, Cr.
Kulepis samatha, M. Papilio antiphates, Cr.
Prothoé regalis, Bil. doson, Feld.
Euripus halitherses, Westw. acheron, M.
Myrina etolus, F. —— sarpedon, L.
Dercas Verhuellii, Hoev. agamemnon, L.
Ixias evippe, Dr. xenocles, Gir.
Hebomoia glaucippe, Z. Protoparce orientalis, Bil.
Prioneris thestylis, Gir. Amesia aliris, DO.
Appias galba, Wall.
There is therefore nothing in the Lepidoptera received in
the present collection, with the exception of the Malayan
genus Prothoé and the new species of Hiposcritia, which
might not have been obtained at Assam; even the presence
of Prothoé in Assam would not astonish me, since not a few
Malayan types range quite as far northwards, even the same
species being caught in Assam and Borneo ; the present series
from the vicinity of Assam fully bears out this fact.
Dr. Watt fully expected to remain at Manipur for three
years, but was most unfortunately recalled soon after his
arrival there; so that the collection is doubtless by no means
so complete as we could wish; still, as next to nothing is
known of its fauna, every addition must needs be welcome,
and, considering how little opportunity Dr. Watt had of
making a collection at all, owing to numerous other occupa-
tions, the series of species sent home by him is by no means
an insignificant one.
Nymphalide.
Huritq@inz.
1. Caduga melaneus, var.
Puyilio melaneus, Cramer, Pap. Exot, i. pl. xxx. D (1775),
Manipur.
Only one injured example of this species was obtained. -
300 Mr. A. G. Butler on Lepidoptera from
2. Parantica melanoides.
Parantica melanoides, Moore, P.'Z, S. 1883, p. 247. n. 1.
One pair. Borders of Assam.
3. Limnas chrysippus.
Papilio chrysippus, Linneeus, Mus. Lud. Ulr. p. 263 (1764).
Males only. Near Assam.
4, Salatura genutia.
Papilio genutia, Cramer, Pap. Exot. iii. pl. ecvi. C, D (1782).
Three pairs. Near Assam. -
5. Tirumala septentrionalis.
Danais septentrionalis, Butler, Ent. Month. Mag. xi. p. 163 (1874).
Three pairs. Near Assam.
6. Danisepa rhadamanthus.
Papilio rhadamanthus, Fabricius, Ent, Syst. iii. 1, p. 42. n. 127 (1798).
A male. Near Assam.
7. Penoa alcathoé.
Danais alcathoé, Godart, Enc. Méth. ix. p. 178. n. 5 (1819).
go ¢. Near Assam.
8. Penoa deione.
Euplea deione, Westwood, Cab. Orient. Ent. pl. xxxvii. fig. 3 (1848).
A male. Near Assam.
9. Trepsichrois Van-Deventert.
Trepsichrois Van-Deventeri, Forbes, Nat. Wand. p. 274 (1885).
A series. Near Assam.
10. Lsamia trawada.
Euplea irawada, Moore, Ann. & Mag. Nat. Hist. ser. , vol. xx. p. 45
(1877).
Isamia trawada, Moore, P. Z. 8. 1883, p. 311. n. 2.
One beautiful male. Near Assam.
Manipur and the Borders of Assam. 301
SATYRINZ.
11. Anadebis himachala.
Mycalesis? himachala, Moore, Cat. Lep. E. I. Co. 1. p, 234, n. 5038
(1857).
One poor specimen. Near Assam.
12. Lethe latiaris.
Debis latiaris, Hewitson, Exot. Butt. 111. Debis, pl. i. fig. 4 (1862).
2. Near Assam.
13. Lethe verma.
Satyrus verma, Kollar, in Hiigel’s Kaschmir, iv. 2, p. 447, pl. xvi. figs. 1,
2 (1848).
@. Near Assam.
14. Callerebia orixa, var.
Callerebia orixa, Moore, P. Z. 8. 1872, p. 555.
6. Near Assam.
Differs from the typical male (from the Khasia Hills) in
the narrower zone to the ocellus of the primaries, which is
also more oval in form, the obsolete character of the ocellus
on the secondaries, and the absence of the ocelli and greyer
tint on the under surface of these wings: it may prove to be
distinct; but as only one somewhat rubbed example was
obtained, it would at present be premature to separate it.
15. Pachama mestra, var.
Mycalesis mestra, Hewitson, Exot. Butt. iii. Mycal. pl.i. figs. 2, 3
(1862).
¢. Near Assam. ;
The single example obtained differs from the type in its
slightly smaller ocelli, the narrower white band, and greyish
instead of whitish sinuated submarginal stripe on the underside.
16. Calysisme peribea ?
Papilio peribea, Fabricius, Ent. Syst. iii. 1, p. 234. n. 730 (1793).
9. Near Assam.
The single example obtained is somewhat worn and shat-
tered; it corresponds fairly well with the description by
Fabricius, but may be distinct; it chiefly differs from C.
mamerta of Cramer in the greater width of the yellowish-white
band on the under surface, the general greyish coloration, the
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 21
302 "Mr. A. G. Butler on Lepidoptera from
greater width between the two submarginal lines, the inner
one of which is less strongly undulated, and the smaller and
less prominent ocelli, only two on the under surface of the
primaries being at all easily seen.
17. Gareris sanatana.
Mycalesis sanatana, Moore, Cat. Lep. E. I. Co. i. p. 231. n. 489 (1857).
&. Near Assam.
18. Ypthima nareda.
Satyrus nareda, Kollar, in Hiigel’s Kaschmir, iv. 2, p. 451 (1848).
Two pairs. Manipur, Nov. 15th.
The specimens are unfortunately much shattered.
19. Ypthima methora.
Ypthima methora, Hewitson, Trans. Ent. Soc. ser. 3, vol. ii. p. 291,
pl. xviii. figs. 20, 21 (1865).
A pair. Near Assam.
20. Ypthima ordinata ?
Ypthima ordinata, Butler, P. Z. 8. 1880, p. 148. n. 5, pl. xv. fig. 3.
9. Near Assam.
_ The single example obtained is a good deal worn; it agrees
far more closely with Y. ordinata than with any other species
hitherto described, especially in the size of the metallic pupils
to the ocelli of the primaries and in general coloration: the
ocelli on the under surface do not, however, form a perfect
series, as in my type; they are a little smaller, and arranged
in pairs. ‘The type of Y. ordinata was from Bengal.
Eiiyunrin2z.
21. Elymnias leucocyma.
Biblis leucocyma, Godart, Enc. Méth. ix. p. 326. n. 3 (1819).
9. Near Assam.
MorpHinz.
22, Thaumantis diores.
Thaumantis diores, Doubleday, Ann. & Mag. Nat. Hist. ser. 1, vol. xvi.
p. 234 (1845).
Three examples. Manipur.
The specimens are a little worn; two of them are males.
Manipur and the Borders of Assam. 303
23. Thaumantis camadeva.
Thaumantis camadeva, Westwood, Cab. Orient. Entom. pl. iv. (1848).
Hight beautiful specimens. Manipur.
NYMPHALINE.
24. Argynnis Childrent.
Argynnis Childreni, G. R. Gray, Zool. Miscell. p. 33 (1841) ; Lep. Ins,
Nepal, p. 11, pl. xi. (1846).
Two males. Near Assam.
25. Argynnis niphe.
Papilio niphe, Linneeus, Syst. Nat. i. 2, p. 785. n. 208 (1767).
A series of both sexes. Near Assam.
The specimens of this and most of the Assamese species
which were obtained by Dr. Watt during his journey are in
a much rubbed and generally worn condition, whereas those
obtained at Manipur are carefully collected, and consequently
in a very fair state of preservation.
26. Cirrochroa aoris.
' Cirrochroa aoris, Doubleday and Hewitson, Gen. Diurn. Lep. pl. xxi.
fig. 1 (1848).
gd. Near Assam.
27. Ctrrochroa rotundata.
Cirrochroa rotundata, Butler, Trans. Linn. Soc., Zool. (2) i. p. 543
(1877).
Near Assam.
Fourteen more or less worn specimens were obtained.
28. Atella sinha.
Terinos sinha, Kollar, in Hiigel’s Kaschmir, iv. 2, p. 488 (1848).
Near Assam.
29. Cethosia biblis.
Papilio biblis, Drury, Il. Exot, Ent. i. pl. iv. fig. 2 (1773).
g. Near Assam.
30. Cethosia cyane.
Papilio cyane, Drury, Ill. Exot. Ent. i, pl. iv. fig. 1 (1773).
a2. Near Assam.
21*
304 Mr. A. G. Butler on Lepidoptera from
31. Parthenos gambrisius..
Papilio gambrisius, Fabricius, Ent. Syst. iii. 1, p. 85. n. 264 (1793).
dé. Near Assam.
32. Modusa procris.
Papilio procris, Cramer, Pap. Exot. ii. pl. evi. E, F (1779).
Manipur.
33. Athyma cama.
Athyma cama, Moore, Cat. Lep. E. 1. Co. i. p. 174, n. 357, pl. v. a.
fiz. 5 (1857).
$- Manipur.
34. Athyma selenophora.
Limenitis selenophora, Kollar, in Hiigel’s Kaschmir, iv. 2, p. 426,
pl. vil. figs. 1, 2 (1848).
¢. Near Assam.
35. Athyma zeroca.
Athyma zeroca, Moore, P. Z. S, 1872, p. 564.
¢. Near Assam.
36. Athyma mahesa.
Athyma mahesa, Moore, Cat. Lep. EK. I. Co, i. p. 176. n. 360, pl. v. a.
fig. 7 (1857).
&. Near Assam.
One somewhat melanized specimen, evidently belonging to
this species.
37. Athyma inarina.
Athyma nara, Moore (nec Doubl.), P. Z. 5. 1858, pl. 50. fig. 6.
A comparison of the two figures representing A. dnara will
at once decide their specific distinctness, the commoner species
figured by Moore having the orange and white bands consider-
ably narrower than in the typical form represented in the
‘Genera of Diurnal Lepidoptera.’
o. Near Assam.
38. Athyma leucothoé.
Papilio leucothoé, Linnzeus, Mus. Lud. Ulr. p. 292 (1764).
G@. Near Assam.
Manipur and the Borders of Assam. 305
39. Neptis, sp. n.
Allied to N. intermedia, but too much damaged to be fit
for description, especially from a unique example.
Near Assam.
40. Neptis mananda.
Neptis mananda, Moore, P. Z. 8. 1877, p. 586, pl. lviii. fig. 4.
Near Assam.
41. Neptis astola.
Neptis astola, Moore, P. Z.S. 1872, p. 560.
Near Assam.
42. Neptis Swinhoet.
Neptis Swinhoei, Butler, P. Z. S, 1883, p. 145, n. 4.
Near Assam.
43. Rahinda hordonia.
Papilio hordonia, Stoll, Suppl. Cramer, pl. xxxiii. figs. 4, 4 d (1790).
“¢ Ascent to Manipur from Cachar, Dec. 1881.”
44, Huthalia teuta.
Adbvlias teuta, Doubleday and Hewitson, Gen. Diurn. Lep. pl. xliv,
fig. 2 (1850).
3. “ Barak river, on ascent to Manipur, Dec. 1881.”
45. Symphedra cyanipardus.
Symphedra cyanipardus, Butler, P. Z. 8. 1868, p. 618. n. 4.
g- Near Assam.
46. Symphedra dirtea.
Papilio dirtea, Fabricius, Ent. Syst. iii. 1, p. 59. n. 184 (1798).
g. Manipur.
47. Apatura chevana.
Athyma chevana, Moore, P. Z, 8. 1865, p. 763, pl. xli. fig. 1.
dg. Near Assam.
306 Mr. A. G. Butler on Lepidoptera from
48. Hulepis samatha.
Charaxes samatha, Moore, P. Z. S. 1878, p. 831. —
Eulepis samatha, Moore, Lep. Ceylon, i. p. 29, pl. xiv. figs. 24, 26
(1880).
Mylang River, Dec. 1881.
49. Haridra agna.
Charaxes agna, Moore, P. Z. 8. 1878, p. 832.
g. Near Assam.
50. Haridra hindia.
Charaxes hindia, Butler, Lep. Exot. p. 99, pl. xxxvii. fig. 5 (1872).
&. Near Assam.
51. Haridra khimalara.
Charaxes khimalara, Butler, Lep. Exot. p. 97, pl. xxxvii. fig. 1 (1872).
g. Near Assam.
52. Haridra dolon.
Charaxes dolon, Westwood, Cab. Orient. Ent. pl. xxvii. figs. 2, 3
(1848).
Near Assan.
53. Prothoé regalis. (Pl. VIII. fig. 1.)
Prothoé regalis, Butler, Ann. & Mag. Nat. Hist. vol. xvi. pp. 53, 54
(July 1885).
Basal third of wings and body above olive-green: pri-
maries crossed obliquely from the middle of costa to the third
fourth of the inner margin by a broad silvery-blue belt, the
external edge of which is irregularly notched and only sepa-
rated by a blackish submarginal streak from three large spots
of the same colour upon the centre of the external border ;
veins slenderly black, terminating in blackish spots, two of
which are placed between the above-mentioned blue spots ;
two white spots followed by a blackish streak upon the costal
part of the blue belt; a large triangular black spot closing
the discoidal cell; apical area chocolate-brown; three sub-
apical spots, the upper two large, placed obliquely, bluish,
with white centres, the third submarginal, bluish, small:
secondaries with the centre of the wing blue-black; apical
area and external border chocolate-brown ; two linear apical
blue dashes and a blue lie along the base of the fringe.
Manipur and the Borders of Assam. 307
Under surface of primaries whity brown, slightly tinted with
greenish towards the base and with lilacine along the external
border; markings very similar to those of P. Francki, but
the outline-spots on the discoidal area filled in with dark
olivaceous, with no trace of an oblique white band and with
all the internervular submarginal markings cruciform: secon-
daries with the basal half as in P. Franck, excepting that
the discoidal spots are filled in with dark olivaceous ; exter-
nal half considerably darker, its inner half greyish olivaceous,
enclosing a series of oblong internervular black patches,
which are sinuated in front and bounded by reddish crescentic
borders; immediately beyond these reddish crescents is a
submarginal series of eight unequal black-edged bronze-
green spots, with brighter green borders; these spots are
irrorated and more or less suffused with blackish; from apex
to second median branch is a series of gradually increasing
marginal black spots, edged externally with pink, the last
two crossed by a red stripe; a large bright olive-green semi-
circular spot, with black inner border and bluish-white outer
border at outer extremity of first median interspace, and a
large black spot, crossed by a red A-shaped marking, and
bordered along its infero-exterior border with grey, at extre-
mity of interno-median area ; a triangular black and red spot
at extremity of abdominal fold. Hxpanse of wings 80 millim.
Manipur.
On the upper surface this beautiful species may be at once
distinguished from P. Francki of Java by the broader, more
irregular, and greyer blue belt across the primaries, the
absence of a white band on this belt, the blue marginal spots,
and the blue or bluish subapical spots ; the secondaries also
have blue instead of white marginal dashes at apex, and the
external border and apical area are chocolate-brown instead
of purplish brown.
54. Eurhinia fulva.
Rhinopalpa fulva, Felder, Wien. ent. Monatschr. iv. p. 399. n. 21 (1860),
Near Assam.
55. Cyrestis thyodamas.
Cyrestis thyodamas, Boisduval, in Cuv. Régne Anim. Ins. ii. pl. exxxviii.
fic. 4 (1836).
Near Assam.
This species has long been confounded with the following,
which, if not distinct, must surely, I think, be a seasonal
form; it has probably been assumed (without examination)
to be the female of C. thyodamas. :
308 Mr. A. G. Butler on Lepidoptera from
56. Cyrestis ganescha.
Amathusia ganescha, Kollar, in Hiigel’s Kaschmir, iv. 2, p. 480, pl. vii.
figs. 3, 4 (1848).
Near Assam.
This is a yellow insect, with most of the markings on the
wings of a deeper yellow, a few only remaining black ; the
apical area is not smoky brownish, as in C. thyodamas. If it
be a seasonal form of the preceding, one form must have been
just disappearing as the other emerged from pupa, for in no
other way can one account for both of them having been
taken by Dr. Watt at about the same time.
57. Huripus halitherses.
Euripus halitherses, Westwood and Hewitson, Gen. Diurn. Lep.
pl. xli. fig. 2 (1850).
gd. Ascent to Manipur from Cachar, Dec. 1881.”
Only a single damaged specimen was obtained ; the female
(which we have received from Cachar) is the form to which
Mr. Moore gave the name of Hestina isa; we have it also in
both sexes from Dayjiling.
58. Junonia asterie.
Papilio asterie, Linnzeus, Syst. Nat. i. 2, p. 769. n. 183 (1767).
Near Assam.
59. Junonia enone.
Papilio enone, Linneus, Mus. Lud. Ul. pp. 274, 275 (1764).
Near Assam.
60. Junonia orithyia.
Papilio orithyia, Linneeus, Mus. Lud. Ulv. p. 278 (1764).
Near Assam (eighteen examples).
Under this name a number of local forms are usually
associated, all of which appear to be constant. The true J.
orithyia is a Chinese species ; it ranges into Japanand Siam,
but I am doubtful whether it is identical with the Indian
form or forms; it certainly appears to be distinct from the
species obtained by Col. Swinhoe in Mhow and Poona, a good
series of which, owing to his liberality, we possess, and all of
which are decidedly paler on the under surface than the
Chinese insect, and have the pale markings on the apical
area of the primaries above quite white; the latter form also
Manipur and the Borders of Assam. 309
is uniformly smaller, and the blue areas upon the wings are
less tinged with green. I think that in calling this local form
J. Swinhoet I am separating as good and constant a type as
that of Java, named J. ocyale by Hubner, that of Malacca,
to which Mr. Distant has given the name of J. Wallace?, or
that of Turkey and Arabia, recently named by Mr. Lang;
those who maintain that all these forms should still be com-
mingled under the name of J. orithyta are perfectly at liberty
to hold that opinion—the fact of the existence of local diffe-
rences still remains.
61. Symbrenthia hippoclus.
Papilio hippoclus, Cramer, Pap. Exot. iii. pl. cexx. C, D (1782).
Near Assam. —
62. Hestina nama.
Diadema nama, Doubleday, Ann. & Mag. Nat. Hist. xvi. p. 282 (1845).
Near Assam.
The genus to which the following species belongs has hitherto
been placed in this part of the Nymphaline ; I have, however,
not the least doubt (in spite of its short thickened antenne) that
its proper place is in the Satyrinee between Zethera and Orinoma;
the neuration of the wings is almost identical with that of the
latter genus. M. Oberthiir’s notion that Calinaga should be
placed among the Papilionide shows that he has not examined
its structure ; no Papilio has aborted front legs.
63. Calinaga brahma, sp. n.
Nearly allied to C. buddha, but both sexes suffused with
greyish, especially in the discoidal cell of primaries, so that
the bands across and at the end of the cell are blurred and
indistinct ; the elbowed discal series of spots more or less
suffused and reduced in size, as are also the spots beyond the
cell of secondaries ; the extremity of the cell in these wings
is partly filled in with grey; the thorax is of a more orange
tint than in C. buddha. Hxpanse of wings, ¢ 91 millim.,
? 101 millim.
Near Assam.
Two males and a female were obtained.
64. Ergolis merione.
Papilio merione, Cramer, Pap. Exot. i. pl. Ixxxvi. H, F (1779).
Near Assam.
310 Geological Society.
65. Kallima inachis.
Paphia inachis, Boisduval, in Cuvier’s Régne Anim. Ins, ii. pl. exxxix.
fig. 3 (1836).
Near Assam.
ACRAINA.
66. Pareba vesta.
Papilio vesta, Fabricius, Mant. Ins, ii. p. 14. n. 180 (1787).
Near Assam.
Fifteen examples were obtained, showing the usual varia-
tions in colour and pattern.
Erycinide.
67. Zemeros fleqyas.
Papilio flegyas, Cramer, Pap. Exot. iii. pl. cclxxx. KE, F (1782).
Near Assam.
68. Adbzsara fylla.
Taxila fylla, Westwood and Hewitson, Gen. Diurn. Lep. pl. Ixix.
fig. 3 (1851).
Near Assam.
[ To be continued. ]
PROCEEDINGS OF LEARNED SOCIETIES.
GEOLOGICAL SOCIETY.
June 10, 1885.—Prof. T. G. Bonney, D.Sc., LL.D., F.R.S.,
President, in the Chair.
The following communication was read :—
“Note on the Sternal Apparatus in Jguanodon.” By J. W.
Hulke, Esq., F.R.S., V.P.G.8.
The author remarked that although parts of the pectoral arch of
Iguanodon had been identified in this country and in Belgium, nothing
definite was known of the structure of the sternum itself, and stated
that a specimen in the collection of Mr. Beckles, from the Wealden
of Hastings, seemed to throw some light upon this point. The
specimen in question consists of an azygos bar, from near one end
of which two smaller rods diverge laterally, the latter terminating
Geological Society. 311
mesially in expanded ends, applied to what the author regarded as
the ventral surface of the azygos bar, where they approach each other
very closely. These two diverging bones are regarded by the author
as the clavicles. All the evidence tends to show that the parts are
in their normal relations, in which case the clavicles bear the same
' relation to the interclavicle as in the pectoral arch of existing
Lacertilia.
The azygos piece is a long flattened bar, widening posteriorly for
some distance from the attachment of the clavicles, and then nar-
rowing slightly to the posterior extremity. The lateral borders
from the clavicles to the widest part are smooth and gently arcuate
for the articulation of the epicoracoid ; behind this they are rough
and apparently non-articular. The author discussed the nature of
the azygos piece, which evidently includes the interclavicle; but
whether it comprises the costal sternum is questionable. There are
no indications of the connexion of ribs with its lateral borders, and
its figure is quite unlike that of the sternum in existing Lacertilia
and Crocodilia. From all its characters the author concluded that
the azygos piece represents only the interclavicle, and he suggested
that the costal sternum may have been cartilaginous, as in existing
Crocodiles.
June 24, 1885.—Prof. T. G. Bonney, D.Sc., LL.D., F.RB.S.,
President, in the Chair.
The following communications were read :—
1. “ Note on the Zoological Position of the genus Microcherus,
Wood, and its apparent Identity with Hyopsodus, Leidy.” By R.
Lydekker, Esq., B.A., F.G.S.
In this paper the author discussed the characters of the genus
Microcherus, Wood, from English Upper Eocene deposits, which
has hitherto been regarded as an Ungulate form, and showed that
it is really an Insectivore. He also indicated that the American
EKocene form Hyopsodus, Leidy, is almost eertainly identical with
Microcherus.
2. “* Observations on some imperfectly known Madreporaria from
the Cretaceous Formation of England.” By R. F. Tomes, Esq.,
This communication contained notes on several species of Cre-
taceous corals. The author considered that Smilotrochus insignis of
Duncan must be referred to the genus Ceratotrochus; that S. granu-
latus, Duncan, was founded on immature specimens of T'rochocyathus
Wiltshirei, Duncan ; that Micrabacia Fittoni, Duncan, is a variety
of Oyclocyathus Fittoni ; that the genus Podoseris, Duncan, and pro-
bably Syzygophyllum, Reuss, are the same as Rhizangia, M.-Edw.
and Haime, and consequently P. mamulliformis, Duncan, and P.
elongata, Duncan, are species of Rhizangia. He further stated that
Turbinoseris, Duncan, is identical with Leptophyllia, Reuss, and
312 _ Miscellaneous.
as the specific name de Fromenteli is preoccupied in the latter genus,
he proposed to substitute the name Leptophyllia anglica, Tomes, for
Turbinoseris de Fromenteli, Duncan. A new species, probably of
Smilotrochus, from the Gault of Folkestone, and a new Jsastraa from
Atherfield were described, and notes added on the occurrence in
British localities of Barysmilia tuberosa, Reuss, B. Cordiert, M.-Kdw. -
and Haime, Plewrosmilia neocomiensis, K. de From., of a small form
of <Astrocenia, and of IJsastrea Reussiana, M.-Edw. and Haime
(= Ulophyllia crispa, Reuss). The occurrence of Beaumontia
Egerton, derived from the Carboniferous Limestone, in the Upper
Greensand of Cambridge, was also recorded.
3. On the Fossil Flora of Sagor in Carniola.” By Constantin,
Baron von Ettingshausen, F.C.G.S.
The author in this paper gave the principal results of his exami-
nation of the fossil flora of Sagor, consisting of 170 genera and
387 species, of which a list was appended. ‘The plants were ob-
tained from 14 different localities, some of the most important species
from each of which were mentioned; in one of these localities
the flora underlying the brown coal of the district belonged to the
uppermost Eocene, whilst the remaining stations were assigned to
the lowest stage of the Miocene system. ‘The great diversity of the
fossil plants showed that the Tertiary flora of this and other localities
must be considered the origin of all the living floras of the globe ;
for in the fossil-flora of Sagor are found plants representative of
forms now found in Australia, North America and Mexico, Cali-
fornia, Chili, India and the East Indian islands, Europe, Africa,
Norfolk Island, and New Zealand. Examples of all these were
cited.
MISCELLANEOUS.
On the Brisingide of the Expedition of the « Talisman.’
By M. Epmonp PERRier.
Tux family Brisingide, which I established in 1875 in my
revision of the Stellerida, at first contained only the genus Brisinga,
and appeared to be completely isolated in the class Stellerida. In
his fine memoir on Brisinga coronata and endecacnemos, Ossian Sars
approximated these remarkable animals to Solaster ; but the form
of their pedicellariw demonstrated, on the contrary, very clearly that
they must be referred to the Asteriad, and from that time I thought
that it was advisable to group in the family Brisingide all the aberrant
Asteriade which had only two rows of ambulacral tubes, that 1s to
say Pedicellaster and Labidiaster. This is also the conclusion to
which Dr. Viguier has been led in his ‘ Anatomie comparée du
squelette des Stellérides *. ;
This conclusion has since been fully confirmed by the study which
Dr. Stiider and myself have been able to make of the Labidzasteres
of the coast of Patagonia: but, further, the genera Hymenodiscus,
* Thése de doctorat, 1879, p. 119.
Miscellaneous. 313
E. P., and Brisingaster, de Loriol, have come to be added to this
family, and to show that the diverse forms which it includes were
of great interest in connexion with the morphology of the dorsal
skeleton of the Stellerida. In fact I have made known one genus,
the genus Hymenodiscus, in which this skeleton is wanting on the
arms, which possess only the ambulacral and adambulacral pieces.
To these pieces are added, in Brisinga, arcs of calcareous pieces
supported by their extremities upon the adambulacral pieces, and
which occur only in the region of the anus, which contains the
generative apparatus. These arcs are still very little developed
in Brisinga mediterranea, K. P. There exists only a single one for
two pairs of adambulacral pieces in B. endecacnemos and coronata ;
there is one for each pair of adambulacral pieces in B. Edwardsii,
K. P. Lastly in Labidiaster and Brisingaster there are added to
these transverse arcs some longitudinal pieces which complete a
calcareous network, closely resembling that which forms the dorsal
skeleton of the Stellerida of the genus Asterias. Notwithstanding
this, by the constitution of their disc and the number of their arms,
the typical Brisingide remained separated from the Asteriadee on the
one hand, and from the Pedicellasteres, their nearest relatives, on
the other. The new Brisingide collected by the ‘ Talisman’ serve
to fill up this gap, and at the same to extend the idea that we must
form of the actual type of the Brisinge. These Brisingide belong
to six forms, which we propose to name Brisinga robusta, B. semi-
coronata, B. elegans, Freyella spinulosa, F. sewradiata, and Coronaster
Parfait. It is to be remarked that the form B. coronata, collected
in abundance by the ‘Travailleur’ in the Bay of Biscay, proved to be
comparatively rare after passing the latitude of Morocco, and was
replaced by the new forms which have just been named.
Brisinga robusta is in a manner only an exaggeration of B.
coronata. It possesses seventeen arms, much swelled in the
neighbourhood of their base, and each attaining a length of more
than two decimetres. Through its very thick integuments we
cannot distinguish the prominent calcareous arcs, furnished with
long spines, which are so distinct in B. coronata ; but the disc and
the bases of the arms are none the less bristling with very numerous
and very strong spines. This form was captured off the Sahara, at
depths of from 882 to 1435 metres. Brisinga semi-coronata, from
the same regions, has likewise from fifteen to seventeen arms; but
its arms are more slender, its disc is furnished with comparatively
small spines, and the spines of the arms, which are less numerous
and rather short, instead of being isolated on each side asin B.
coronata, are arranged in a transverse comb oneach side. Brisinga
elegans is distinguished by its very characteristic flattened form, its
broad and not very prominent disc all of a piece with the arms,
which are slender, comparatively short, and furnished as usual with
transverse calcareous arches, but very scantily spinous. The
number of arms is nineteen ; the colour rose-red. Fifteen individuals
were dredged off the Pilones at a depth of 1435 metres. The three
forms just characterized are true Brisinge.
It is advisable, on the other hand, to create a genus Freyella
Fo iE Miscellaneous.
(from Freya, a Scandinavian goddess) for the form which I have
named B. Hdwardsi, and for the new forms /. spinulosa and
F, sexradiata. In these forms all the inflated portion of the arms
is in fact entirely covered with polygonal plates still arranged in not
very regular arches, equal in number to the adambulacral plates in
B. Edwardsti, of which we possess only one arm, but forming, on the
contrary, a regular mosaic in /. spinulosa and F. searadiata. This
last form, obtained from a depth of 4060 metres, is remarkable for
the small number ofits arms, six only; F. spinulosa, on the contrary,
has from eleven to fifteen, generally thirteen very long arms; it is
of an orange-yellow colour, and when living diffuses a pretty strong
alliaceous odour. It is met with from the Cape Verde to the Azores
at depths of 2000-4000 metres. The Freyelle, which are remarkable
even by the peculiar construction of their skeleton, do not bear large
spines like B. coronata or robusta ; their skeletal plates are smooth
in F. Edwardsii, furnished each with a small prickle in F. sexradiata,
and with a transverse row of small spinules in F’. spznulosa.
Lastly, the Coronasteres in appearance exactly resemble the
species of Aséerias of the group of A. tenwispina, and possess, like
them, a dorsal skeleton reticulated with large meshes. But their
ambulacral tubes are arranged only in two rows, and their spines
are enveloped in a sheath which may ascend nearly to the apex and
which bears an elegant fringe of pedicellariz. The arms, which are
very easily detached from the disc, as in the Brisinge, are eleven in
number. A single specimen was obtained at the Cape Verde Islands
at a depth of 250 metres. Coronaster forms a term exactly inter-
mediate between Lab:diaster and Asterias, and the latter is thus
closely affined to the Brisinge, just as Freyella sexradiata leads
directly from the Brisinge to the Pedicellasteres with five and six
arms. The Brisinge, while still remaining very remarkable forms
and comparatively isolated from the Ophiurans to which they were at
first approximated, are thus, by the new discoveries, more and more
distinctly united with the Stellerida properly so called. From the
point of view of the development of the dorsal skeleton they may be
arranged in an ascending series after the following fashion :—
Hymenodiscus Agassizii, K. P.; Brisinga mediterranea, H. P.; B.
elegans, EK. P.; B. endecacnemos, Asbjérnsen ; B. coronata, KE. P.;
B. semi-coronata, E. P.; B. robusta, E. P.; Labidiaster radiosus,
Lovén; Brisingaster Robillardi, de Loriol; Pedicellaster typicus,
Lovén ; Coronaster Parfaiti, EK. P.; Asterias tenwispina, Lamk.
The Freyelle form an aberrant series.—Comptes Rendus, August 10,
1885, p. 441.
On a new Specres of Land-Tortorse, brought by M. Humblot to the
Museum of Natural History. By M. Léon Varnrans.
The abundance and remarkable variety of specific types presented
by the group of Land-Tortoises in Africa, and especially in the
islands situated to the east of that continent, are facts which have
long been known, and important memoirs have been published upon
this subject, among which it is sufficient to refer to Dr. Gunther's
Miscellaneous. 315
memoir upon the gigantic Tortoises. One may therefore be
astonished at finding in this region an animal of comparatively large
size belonging to this group, and the characters of which do not allow
of its being confounded with any other species of the genus. It is to
one of our most zealous travellers, M. Humblot, that the Museum is
indebted for this curious Chelonian. That naturalist, who was in
possession of seven individuals of it, informs us that the present one,
which is of the size of a large Testudo radiata, was not the largest,
some of them being of nearly twice its dimensions.
The carapace is convex, generally hemispherical, with the anterior
and posterior orifices not much raised, resembling that of T'estudo
raduata, Shaw. The dorsal shield presents a slight constriction
in front, and is rounded behind; there is a nuchal shield, although
it is very small. The form of the plastron particularly characterizes
this species. ‘The gular plate, instead of being double, as is usually
the case in the Tortoises properly so called, is simple, as in the few
species of which Gray proposed to form the genus Chersina; this,
however, is only observed on the lower surface ; on the upper surface
there is a groove, an indication of the usual division. This plate
and the bony part which supports it, distinct from the rest of the
plastron, form a flattened, triangular process, twice as long as the
width of its base, and bent from below upwards, a peculiar arrange-
ment, the singularity of which struck M. Humblot, who observed
it in his seven individuals.
The colour of the dorsal shield is yellowish red, with brown tints
upon the periphery of the scaly plates of the disc and on the limb ;
the plastron, which is uniformly straw-yellow, shows some traces of
a darker tint towards the margin of the abdominal plates. In fact
the general coloration partakes at once of those observed in Testudo
radiata, Shaw, and Testudo (Chersina) angulata, Dum.
These characters enable us at the first glance to distinguish this
Chelonian from the other known true Tortoises; I propose to name
it Testudo yniphora, in allusion to the peculiar form of the anterior
part of the plastron.
Although the origin of this species cannot be precisely fixed, we
may nevertheless regard it as certain, from the information furnished
by the Arab sailors who sold these Tortoises to M. Humblot at the
Great Comoro, that these animals had been captured upon an islet
situated north-north-east of that place; moreover, considering the
prevailing winds at the time, and the method of navigation adopted
by these men, their vessel could only have come from this direction,
that is from a locality situated towards Aldabra, perhaps even a
dependency of that group of islands, where we know of such curious
representations of the family Chersites.— Comptes Rendus, August 10,
1885, p. 440.
Orientation of the Embryo and Formation of the Cocoon in
Periplaneta orientalis. By M. P. Hattez.
M. Hallez finds that each of the sixteen ovigerous tubes in
Periplaneta orientalis contains a chaplet of ova gradually passing
316 Miscellaneous.
down the tube towards the point of exit. He finds that throughout
the organic axis of the ovum is parallel to the axis of the body
of the parent, and, further, that the pole of the ovum which is
directed towards the narrow part of the ovigerous tube, 7. ¢. towards
the head of the mother, is the cephalic pole of the ovum. The
maturation of the ova goes on approximately part passw in all
the tubes, so that at a given moment each tube presents a mature
ovum placed close to the calyx or oviduct, and oviposition and the
formation of the cocoon are then imminent. He describes the
latter process as follows :—
“The serific glands, as Léon Dufour calls them, form at this period
a voluminous bundle ventrally situated and composed of very long
tubes, coiled together, bifid and multifid. These tubes are filled with an
opaque, readily coagulable substance, in which are disseminated an
infinite number of crystals. They are prisms with a rhombic base,
presenting a small rectangular facet of truncature in place of the pro-
jecting edges. They measure, on the average, 15, are insoluble
in water and in weak nitric acid; they are, on the contrary,
destroyed without any disengagement of gas by concentrated sulphuric
acid; and caustic potash dissolves them still more rapidly. These
crystals are destined to the construction of the cocoon, which is
formed by an assemblage of these crystals cemented by the coagu-
lated substance in the midst of which they have originated.
“This cocoon, which Léon Dufour compares to a small, closed
valise, is ovoid and presents a denticulated crest which is the line of
dehiscence. The posterior extremity (that which issues first at the
moment of delivery) is generally a little the thicker; the other is
easily recognizable owing to the presence of a sort of small hilum.
The line of dehiscence is superior, consequently corresponding to the
dorsal surface of the insect. The eggs, sixteen in number, are
arranged in two rows vertically in this cocoon; finally, in more
than 100 cocoons that I have examined I have always found the
heads of all the embryos directed towards the line of dehiscence.
‘“‘T have had the opportunity of observing directly the fabrication
of the cocoon and the arrangement of the eggs in its interior. The
two oviducts debouch a little in front of the subgenital plate at the
superior level of the genital armature...... which is essentially
formed of two episternites and of a sternite with two biramose branches.
The whole forms a sort of funnel or speculum with four mobile
branches, and placed obliquely from in front backwards, and from
above downwards. The egg coming from the oviduct falls into this
funnel, which seizes it and places it side by side with those previously
laid; at the same time, by the combined mechanism of the walls of
the genital sac and the pieces of the armature, the coagulable matter
and its crystals are uniformly spread and take the form of the
cocoon. The line of dehiscence is produced by a pressure. exerted
by the superior part of the sternite and perhaps also by the groove of
the tergite of the anal segment. The cocoon is moreover supported
beneath by the subgenital plates.”
The egg always falls into the genital armature with the caudal
pole downwards.— Comptes Rendus, August 10, 1885, p. 444.
m
ns of two new Species of Araneidea. By the
, M.A. &. (Plate IX. A. figs. 1&2) ...... 237
. iionehip of Ulodendron, Lindley and Hutton,
rnberg; Bothrodendron, Lindley and Hutton ;
i; and Rhytidodendron, ae By Rozert
- te TIT.) BOT SU AiG: ctegtha thren ara en ec 239
- paramecium.. By Sara GweEnpoten Fourxe.
Bee Oe ica ea iar elas ape os aE ee ae 260
the Testaceous Mollusca obtained during a
the Gulf of Suez in the Months of February
jy Rozerr MacAnprew.—Republished, with
. ons, by Atrrep Hanns Cooxz, M.A., Curator in
z oology and Ca Anatomy, tonne:
Bees Wie solar aKa es SiMe ne a RGN GT aac site tease 262
8 of sake from the N ucniaihed of Port
ustralia - By H. J. Carrur, F.RS. &e.. 277
on a Paper by Prof. E. D. Cope on the oe
_ Grande do Sul, Brazil. By G. A. Boununenr. 204
m of Lepidoptera made at Manipur and on the
Dr. George Watt. By Arruur G. Burumr,
BEETS 9 aig “hectares ra ca oe cata a i 298
DINGS OF LEARNED SOCIETIES.
J. W. Hulke on the Sternal Apparatus in
Lydekker on the Zoological Position of the
, Wood, and its apparent Identity with
"Mr. R. F, Tomes on some imperfectly —
from the Cretaceous Formation of England ;
ee vusen on the Fossil Flora of Sagor in Car-
ot AN eg he Rede Ns RMON li Mores ara 310—312
MISCELLANEOUS.
On the Brisingide of the Expedition of ve ‘ ane an M.
BOSD: e PREIER cca Ol pe eaten nE ata ce Gare Shida pace ig aye Sepa ies.
On a new Species of Land-Tortoise, brought by M. Humblot to the
Museum of Natural History. By M. Laon Varrrant ........ 314
Orientation of the Embryo and Formation of the Cocoon in Peri-
planeta orientalis, By M. P. Hatuez .................... 315
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XXX.— Critical Observations on Prof. Leidy’s “ Freshwater
Rhizopods of North America,” and Classification of the
Ehizopods in general. By Surgeon-Major WALticH, M.D.
From the standpoint of the evolutionist any system of classi-
fication to be strictly natural must be based exclusively on
such characters as are indicative of physiological advance in
the class of organisms to which it is applicable ; and, & fortior¢,
every system not so based, and which, in its application, is not
even coincident with readily observable physiological advance,
must necessarily be looked upon as retrogressive and mis-
leading.
With such a self-evident axiom for our guidance it will
probably be admitted by every biologist who is well read-up in
the scientific literature of the Rhizopods that in no class of the
Protozoa has multiplication of genera and species been carried
to a pitch so reckless, and certain, if left unchecked, to plunge
the nomenclature of the entire class into a state of inextri-
eable confusion.
The plea most frequently urged in justification of this
mania for species-manufacture is that it is essential for the
purpose of identifying particular forms. But those who rely
on this plea seem to forget that identification of mere varieties
does not help us in identifying types, and therefore becomes
one of the most vexatious obstacles in the way of natural
elassification ; the greater the tendency to unlimited variation
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 22
318 Dr. Wallich on the Rhizopods.
in any particular group of organisms the greater being the
evil effect of ignoring these considerations. Now it is univer-
sally allowed by all who have systematically studied the tes-
taceous Ameebans, that these organisms are, of all others, the
most liable to extreme variation, in virtue of their being the
most likely to be affected by external conditions and purely
local influences.
Ehrenberg, the great pioneer in microscopic natural history,
in touching upon this subject observed that ‘‘in the remark-
able mode of reproduction by self-division and the indiffe-
rence of these minute independent beings to climatic variation
there appear to reside characters which sufficiently distinguish
them from larger beings, so as to make them preeminently
adapted to a greater duration and extension through entire
and successive formation-epochs of the earth.”—Phil. Mag.
(from Trans. Roy. Acad. Berlin, 1840).
This tersely-expressed opinion has been repeatedly borrowed
by later writers without due acknowledgment, and coupled
with oceasional additions and alterations, which have not
tended to improve, but to impair, its import. In allowing
myself to render it more closely applicable to the particular
group of orgamsms forming the subject of the present
inquiry, it is my earnest wish not to fall under any such
imputation.
The causes affecting the stability, extension by variation,
and extinction of the Protozoan species follow a law which may
be thus stated :—The lower the type the less liable is it to be-
come extinct, but the more liable is it to undergo what may be
termed constructive variation, inasmuch as its simple body-
substance is least powerfully affected by changes in the
material condition of the medium in which it lives, whereas
its protective covering (should it possess one), the basis of
which is invariably chitinoid, and consists of a permanently
consolidated layer of ectosare thrown off from the animal
itself, is the first portion to be acted on by extraneous condi-
tions. We are thus enabled to expla why the body-
substance of the testaceous Rhizopods remains unaltered,
whereas their protective covering presents an almost infinite
varietal range both as regards the materials of which it
is constructed and ihe form the construction assumes.
With these preiiminary remarks before us, let us now inquire
how far the most commonly accepted subdivision of the Rhi-
zopods into orders, viz. that proposed by Dr. W. B. Carpenter,
can be considered a natural one, bearing in recollection,
however, that it is to the generic and specific subdivisions of
the two most thoroughly known families, namely those
Dr. Wallich on the Rhizopods. 319
furnished with shell-like or chitinoid coverings, that attention
is specially invited. The question of subdivision into orders,
although of primary importance as regards the basis of every
system of classification, being in reality of secondary im-
portance for the purpose now in view, is imported into it
solely in order to determine the position of G'romda, con-
cerning which, as will be hereafter seen, there would still
appear to be a great deal of misconception.
According to Dr. Carpenter, the subdivision into orders
may be best accomplished by taking as a basis “ those
structural characters which are most expressive of physio-
logical difference in the form, proportions, and general
arrangement of the pseudopodial extensions; for notwith-
standing their unrestrained polymorphism, the Rhizopods
present three very distinct types of pseudopodian confor-
mation, to one or other of which they may all be referred,
the group thus formed being eminently natural.” Dr. Car-
penter then proceeds to say that ‘‘im cases in which the
differentiation into ectosare and endosare has proceeded
furthest, so that the body of the Rhizopod bears the strongest
resemblance to an ordinary cell, as is the case with Ameba
and its allies, a nucleus may be distinctly traced ; in those, on
the other hand, in which the original protoplasmic condition
is most completely retained (as seems to be the case in Gromia
and with the Foraminifera generally), no nucleus can be
distinguished ” *,
In Dr. Carpenter’s classification Gromia is consequently
made the type of his lowest or Reticularian order, and is
associated in that order with the Foraminifera only. The
same basis of classification would seem to have been adopted
by Prof. Huxley in his “ Hunterian Lectures on the Inverte-
brata,”’ delivered in 1867, when he described the Foraminifera
as a group of Monerozoa containing some of the very
simplest forms of life, one of the simplest of Foraminifera
being Gromia, a jelly-hke mass with extensile pseudopodia
. enclosed in a horny shell, differing from the imperforate Milio-
lidee and Lagenide only in having a membranous or horny
shell f.
In the Ann. & Mag. Nat. Hist. for June 1863 it was
pointed out by me that the nuclear body with its capsular
investment made its appearance for the first time in the two
highest orders, and not in the lowest, which in my system
* ‘The Study of the Foraminifera,’ 1862, pp. 14 and 15.
t “ Roy. Coll. Surgeons: Hunterian Lectures by Prof. Huxley, F.R.S.,
on the Invertebrata.” (Abstract.) Quart. Journ. Microsc. Science,
1868.
2a"
320 Dr. Wallich on the Rhizopods.
comprises the Gromide, Foraminifera, and Polyeystina, the
nuclear granules being in this order diffused, and assuming
the multiple character of sarcoblasts, which, on separation
fiom the parent sareode, constitute the primordial segment
of the new brood. It was then also stated that the con-
tractile vesicle does not make its appearance in the lowest
order, namely the Herpnemata, or the intermediate order, the
Protodermata, but oceurs for the first time in the highest
order, or Proteina, in which are associated together the Acti-
nophryne, Lagynide, and Ameebide, both nueleus and
contractile vesicle being invariably present in all the families
of this order, although sometimes obscured from view in the
testaceous genera. At the period referred to, viz. June 1863,
neither of these two organs had as yet been noticed in Gromia ;
but a few weeks afterwards the discovery of the nucleus in
this Rhizopod was announced as follows:—‘“ As bearing
directly on the characters of the Amcebide I have to record an
important fact which revealed itself during my examination of
the material containmg Amba villosa; | allude to the detec-
tion of a well-marked nucleus and nuclear capsule in Gromia
oviformis. ‘The contractile vesicle I failed to trace, but, in
the presence of the manifest analogy existing between the
Gromide and Lagenide, it is, I think, extremely probable
that this organ also may yet be detected. Should it be so,
the transfer of Gromia from the lowest to the highest ordinal
type of Rhizopod structure would be rendered necessary.” —
Annals, Aug. 1863, p. 123.
Having followed up this subject still further, the following
statement was made by me in the ‘ Annals’ for December of
the same year (p. 450) :—‘‘I may here repeat the statement
made in the ‘ Annals’ for August last, p. 123, that I had
detected a distinct nucleus in Gromta oviformis. At a later
period, but only once, I detected an equally distinct contractile
vesicle. But until further opportunities present themselves
ot determining whether or not these two organs occur univer-
sally in all the members of the genus, I would reserve my
final opinion on the subject.” Finally, m a paper “ On the
Affinities of the Polycystina,” read at the Royal Microscopical
Society in May, and published in Quart. Journ. Microsc.
Science for July 1865, my first tabulated classification of
the Rhizopods appeared, the three orders being defined as
shown opposite :—
321
Dr. Wallich on the Rhizopods.
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a22 Dr. Wallich on the Rhizopods.
Under the head of characters relating to the Proteina it was
further stated that the presence of two such organs as the
nucleus and contractile vesicle must be regarded as of primary
importance, reasons having already been assigned for con-
sidering the degree of differentiation of the sarcodic body
alleged to be deducible from the shape, form, proportions, and
arrangement of the pseudopodia as of merely secondary value ;
and that, after a laborious study of the freshwater Proteina
extending over nearly two years, without any important inter-
mission, I felt satisfied that, even if made the basis of generic
subdivision, these pseudopodian characters ‘ are subject to a
much wider range of variation than is usually imagined, not
only in the same genus, but in the same individual at diffe-
rent periods of its existence ” *.
It was during the above-mentioned continuous study of the
Proteina that I verified the fact of the presence of a contrac-
tile vesicle in Gromia in a sufficiently large number of cases
to place the matter beyond doubt. This was mentioned in
a paper “ On the Fundamental Error of constituting Gromia
the Type of Foraminiferal Structure,” published in the
‘Annals’ for Feb. 1877, p. 168.
Meanwhile, however, Dr. Carpenter had brought out the
fifth edition of his most excellent treatise on ‘ The Microscope,’
and had so far modified his views as to insert the following
remark respecting the characters upon which he still depended
for the subdivision of the Rhizopods into orders :—“ It must be
freely admitted,” he said, ‘ that these groups [the Reticularia,
Radiolaria, and Lobosa] cannot be distinctly marked out, the
typical examples which will now be described being connected
by many intermediate forms. ‘This is not to be wondered at
when the extreme indefiniteness which characterizes the
lowest type of animal life is duly borne in mind. ... . In
Gromia, moreover, we have an example of a Rhizopod which
very characteristically exhibits the Reticularian type in the
disposition of the pseudopodia, but which Dr. Wallich was
the first to point out possesses both a nucleus and contractile
vesicle, thus showing a transition to the higher orders.” —Op.
cit. pp. 168, 169.
It needs no argument of mine to prove that a more illo-
gical and hazardous conclusion could not have been drawn
from so very significant a fact, for, instead of the altered
position of Gromia being im anywise accounted for by at-
* For details of the grounds on which I rested my statements con-
cerning the worthlessness of ordinal and generic characters derived from
the pseudopodia see papers on the Rhizopods in the ‘Annals’ for Noy.
1865 and Dec. 1868.
Dr. Wallich on the Rhizopods. 323
tributing the previously so-called typical characters of its
pseudopodia to its transitionary tendency, these characters,
when taken in conjunction with the vastly more important
presence of the nucleus and contractile vesicle, which alone
imdicate the true systematic position of the organism, proved
at once that the Reticularian type, as well as every other
pseudopodian type, could no longer be received as indicative
of physiological advance, and consequently could no longer be
considered of any practical value in the subdivision into orders
of the various families of Rhizopods.
Having thus shown how the case stood in the year 1877,
it will now be necessary to redirect our attention to the years
1863-4, when I called attention for the first time in the
‘Annals’ to the occurrence in this country and elsewhere of
an extensive and highly interesting series of testaceous
Rhizopeds which, with three exceptions to be referred to
hereafter, had not previously been described and figured by
any other writer. ‘T'wo of these excepted forms were in-
eluded in Ehrenberg’s famous-work ‘ Die Infusionsthierchen,’
published in 1839, but without any observations beyond a
somewhat imperfect description of their external characters,
due no doubt to the inferier nature of the microscopic appli-
ances then available. In these circumstances, and in entire
ignorance of the fact just stated, I described and figured the
two forms in question, together with the remainder of the
really new and typical varieties of Difflugia which had been
discovered by mein India and in this country, in the ‘ Annals’
tor June and December 1863 and March 1864.
The whole of these forms, which, for reasons to be presently
given, were referred by me to the genus Diffugva, threw an
entirely new light on the relations borne by the animal to the
shell, or (as it ought to be called in the case of the testaceous
Rhizopods) the test *, which the animal inhabits but is
only to a certain extent instrumental in constructing. The
clue to this most interesting and till then novel fact had
revealed itself to me in some of the living organic forms
obtained in soundings made in the North Atlantic in 1860 on
board H.M.S. ‘ Bulldog’ +, the tubes of certain minute
* It would rid us of a very troublesome source of uncertainty and con-
fusion were the term shell contined to the shells of the Foraminifera ; skele-
ton or framework to the internal siliceous structure of the Polycystina,
Acanthodesmidz, and Dictyochidee ; and tests to the more or less chitinoid
coverings of the Difflugide, Lagynide, and allied forms. As it is, these
terms are employed indiscriminately and without any definite meaning
attaching to each.
+ ‘The North-Atlantic Sea-bed, G. C. Wallich, 1862, part 1, pp. 146,
147 ; and ‘ Biology of Globigerima, 1876, pp. 11 and 12.
324 Dr. Wallich on the Rhizopods.
Annelids being invariably found made up of mineral particles,
with sponge-spicules and minute Globigerine shells, or a
mixture of these in proportion as the mud at the bottom of the
ocean, on which the creatures lived, was more or less com-
posed of varying quantities of these materials. This opens
out avery important question, which may be expressed as
follows :—-Is there, or is there not, any connexion in a physio-
logical sense between increased or diminished complexity of
structure in the tests of the various testaceous families, and an
increased or diminished complexity in the organization of the
creatures inhabiting them ? I‘or, should the answer be in the
negative, the only reasonable inference to be drawn from the
facts is that mere differences in the material, mode of build-
ing up, and outward form and appearance of the tests, furnish
no trustworthy characters for generic or even specific distinc-
tion. Or, to take the case of the Foraminifera, it equally be-
comes a question whether increased complexity in what Dr.
Carpenter very appropriately calls “the plan of growth” of
the shells can be regarded as indicating coexistent increase or
decrease in the complexity of organization of the animal to
which the tests belong. In this instance, however, it seems
out of our power, in the present state of what ought to be
termed our ignorance rather than our knowledge, to furnish
any satisfactory answer, inasmuch as no means or methods of
observation are available, even with the highest powers of
the microscope, which can enable us to resolve those subtle
traces of organization, the existence of which we may suspect,
but cannot demonstrate. To assert, however, that highly com-
plex functional effects take place in the bodies of these so
termed unsurpassably simple creatures, in the absence of any
adequate signs of organization, is so absurd that the wonder
is that such a proposition should ever have been seriously pro-
pounded and unreservedly accepted. In touching on the
same question in relation to a very different class of organisms,
namely the Desmids and Diatoms, the case was thus stated
by me :—‘‘ We know that complex vital processes are carried
on in even the lowest types of being. But because we neither
know nor are able to conceive how they are carried on we are
not warranted in taking for granted that what appears to us,
even with our most refined appliances, to consist of a mere
particle of structureless jelly, must necessarily be as primor-
dially simple as it appears” *.
To this opinion I would still adhere: but a voice infinitely
* « Aye the Desmids and Diatoms ‘Simple Cells’?” G,C. Wallich,
‘Popular Science Review,’ April 1877, p. 161.
Dr. Wallich on the Rhizopods. 325
more potent than mine has spoken on the same subject, and
in words too pregnant with meaning and truth to be dis-
puted. I allude to Prof, Tyndall, who writes as follows :—
““ Have the diamond, the amethyst, and the countless other
erystals formed in the laboratory of nature and of man no
structure? Assuredly they have; but what can the micro-
scope make of it? Absolutely nothing. It cannot be too
distinctly borne in mind that between the microscope and the
true molecular limit there is room for infinite permutations
and combinations. Jt as in this region that the poles of the
atoms are arranged, that tendency is given to their powers, so
that when poles and powers have free action, proper stimuli,
and a suitable environment, they determine first the germ and
afterwards the complete orgunism.’—Iragments of Science,
London (6th edit.), 1879.
It only remains for me to point out that attention was not
invited to the ‘ potentialities ” of organization in the sarcodic
bodies of the Rhizopoda, with a view of bringing them to
bear on the questions we are now engaged in investigating,
but solely to show that the existence of these potentialities
ought to be recognized, although for the present we must rest
content to avail ourselves of such characters as are made
palpable to our senses with the aid of the microscope.
This being clearly understood, let me observe that no
satisfactory evidence has as yet been discovered of any generic
difference between the animal we call Ame@ba and the animal
we call a Diflugia beyond the palpable one which hinges on
the fact of the former being a naked and the latter a testaceous
Rhizopod. The sarcode-body in both presents the same degree
of differentiation into what is known as endosare and ectosare.
In both it is provided with a nucleus and contractile vesicle. In
both there is a definite anterior and posterior part, the function
of the latter being to exercisea certain degree of prehensile action,
that is to say to the extent of regulating the movements of the
body in the naked forms and maintaining its position within
the test in the testaceous ones. In both there occur sarco-
blasts, oil-globules, and crystalloids ; and in both we may
observe extensive vacuolation and the gradual development
of a membranous investment of the entire body-substance
when encystation is about to take place.
But if outward characters are to be taken at all as our
guides, the identity of the two animals in Ameba and Difflu-
gta can be shown in a still more striking manner. Thus it
frequently happens that a Difflugian Ameha will vacate its
test whilst under observation, and sally forth as a naked
Ameba without appearing to have sustained any injury or
326 Dr. Wallich on the Ithizopods.
suffered any inconvenience. And it happens just as com-
monly that an ordinary naked Ameba will, whilst under ob-
servation, take summary possession of the first empty Difflugian
or Arcellian test that comes in its way, and at once make
itself quite at home in its new quarters; the newly-assumed
characters being in each instance so perfectly sustained as to
leave an observer who has not actually witnessed the trans-
formation no reason to suspect the now testaceous form to have
ever been otherwise than testaceous, or the now naked form
otherwise than naked.
Other analogies and identities of procedure might be cited,
as, for example, those connected with the process termed
zygosis, of which nothing is in reality known, though several
hypothetical explanations have been hazarded on the subject.
So far, then, we encounter no anomaly; but should we push
our investigations a step or two further we find ourselves con-
fronted by what at first seems to be not only an unrecognized
anomaly, but a paradox. And here Gromia retaliates on
those who once degraded it, not only by refusing to throw
any light on the difficulty, but by doing its best to lend force
toit. F ormerly, as we now are aware, Gromia was wrongly
held to be the type of “the very simplest form of [oramini-
fer,” by virtue of the so-termed Reticularian type of its pseudo-
podia. Yet in recognition of its possessing a nucleus and
contractile vesicle, it has been promoted to the highest status
in the Rhizopod scale. Its test is one of the simplest to be
met with in the highest order, and, when it stood side by
side with the simplest Biloculine Miliolide in the lowest
order, was firmly believed to be just as simple in organi-
zation as they. But we have it on the authority of Dr.
Carpenter, who probably knows more than any other man
living of the structure and “plan of growth” of the shells of
the Foraminifera (and any one who has under his guidance
studied these exquisitely formed structures must have arrived
at the same conclusion), that the Foraminifera, which stand
at the very bottom of the Rhizopodal series in point of bodily
organization, possess ‘‘ shells which are unsurpassed in sym-
metry and complexity of structure by any testaceous or-
ganisms”*,
On the other hand, we see in the highest order of the
Rhizopods the animal of Difiugia and its now firmly esta-
blished compeer (as regards complexity of bodily organization)
both in possession of protective coverings, the extreme szmpli-
city of which is “‘ unsurpassed by that of any other organisms !”
* <The Study of the Foraminifera, by Dr. Carpenter, F.R.S., 1862,
Preface, p. vill.
Dr. Wallich on the Rhizopods. 327
In the case of the Difilugide there is no anomaly. For,
although in the tests of the new forms to which I shall
hereafter have occasion to refer in detail, some singularly
striking characters become noticeable, there is, strictly speak-
ing, no complexity in their construction as imparted to them
by the animal, but only a very exceptional character, which
carries with it indisputable evidence of not being the result of
inherited idiosyncrasy, but of the variable nature of the condi-
tions present in the medium in which the animal lives. This
view was strongly urged by me in my paper in the ‘ Annals’
for March 1864, and in a previous paper in the same Journal
for Dec. 1863, in the following words:—‘ At the most, therefore,
mere modifications in the shape and proportionate quantities
of the organic and inorganic elements entering into the for-
mation of the shell, ought to be employed only in dis-
criminating between species.”—Annals, June 1863, p. 452.
And again:— Assuming from the facts which have been
advanced that the shape, materials, size, and colour of the
Difflugian tests furnish characters so conspicuously variable
as to yleld no trustworthy criterion for even generic or even
true specific distinction, and recalling to mind once more that
the animal is in every instance specifically the same, it
appears to me impossible to arrive at any other conclusion
than that the whole of the subspecies, as well as their inter-
mediate varieties (widely though some of these seem to differ
from others in external features), have not only been derived
by direct descent from a single progenitor, but may still con-
tinue to be produced by direct descent from varieties which
become permanent *; and may one and all still be produced
from a common archetype under the varying conditions to
which these lower forms of life are subject. ‘The animal does
not vary, but it modifies the architecture of its habitation and
the mineral material of which that habitation is in a great
measure constituted, in obedience to local conditions and its
own requirements.” —Annals, March 1864, p. 239.
*« Permanent ” only in the sense of being so as long as the conditions
under which the species or variety first became established remain unchanged.
When these conditions become gradually or suddenly modified, so do the
species or varieties, but only in those respects in which the conditions effect
a change in the animal itself, in its shelly covering, or in both combined.
Thus, a dry season or a flood, or extreme degrees of temperature in the
medium in which the animals live, scarcity or deterioration in the food-
supply, one and all bring about modifications which then tell on their
stability, their tendency to variation, or their extermination. This, in all
probability, is the reason why we so often find some special form we have
been accustomed to look for in a given locality, either replaced bya
varietal form or gone altogether.
325 Dr. Wallich on the Rhizopods.
But it would obviously be the height of rashness and an
indication of great want of discriminative tact to entertain the
idea that what appears to be a rationally grounded explanation
in the case just cited, stands on a par with that involved in
the construction of all the varied and complex forms of Fora-
miniferal shell. Here we meet with presumptive evidence
of the interposition of some faculty superior in kind to that by
which the creature is enabled to select from the materials
within its reach those materials best adapted for its require-
ments. That the Difflugide, in like manner with other
Protozoa, do possess and are able to exercise some such faculty,
is almost as certain as that two and two make four. Several
extraordinary oceanic examples of this were recorded by me
as long ago as the year 1858, and frequently since that period.
But in the Foraminifer there resides not only a like selective
power, when the necessity arises for its exercise, as we see 1n
the case of the Lituoline and Arenaceous series generally,
when seemingly forced to employ sandy or other particles for
the consolidation of their shells on account of the supply of
carbonate of lime held in solution in sea-water, falling short ;
but likewise a constructive faculty of so marvellous a nature
as to leave us ina state of utter bewilderment at the beauty and
symmetry of construction we see before us. For, be it ob-
served, there is in this instance no tangible basis on which we
could attribute what we see to the interference of some known
extrinsic force, such as chemical affinity or a modified form
of crystallization in presence of a colloid. In this dilemma
how are we to account for so truly extraordinary a phenome-
non exhibiting itself at the very bottom of the animal series ?
On my own behalf I can only confess my utter mability
to suggest a solution of the problem.
The inquiry having thus, step by step, reached the point at
which any special group of characters observable in the testa-
ceous Rhizopods under notice can be tested on the basis laid
down in the opening paragraph of this paper, let us now turn
our attention to Prof. Leidy’s monograph on “ The Fresh-
water Rhizopods of North America,” the most recent and by
far the most beautifully illustrated work on the subject that
has hitherto been published *.
The first point deserving of notice is that Prof. Leidy does
not offer any definite classification of his own of the freshwater
Rhizopods, but confines himself to furnishing a more or less
general outline of classification of the various systems pro-
posed by Dujardin, Heckel, Carpenter, Wallich, Huxley,
* Published at Washington in 1879, under the auspices of the “ United
States Geological and Geographical Survey of the Territories.”
Dr. Wallich on the Rhizopods. 329
Carter, Hertwig, Greef, and others. Indeed, as he himself
admits, “‘ his attention has been more particularly directed
to the discovery and determination of the various forms of
Rhizopods occurring in North America, rather than to the
elaboration of details of structure, habits, modes of develop-
ment, and other matters pertaining to their history, though
these have not been entirely neglected ’”’ (op. cit. p. 2).
The only portion of the volume that appears to me to fall
short of the general standard of technical excellence is the
purely bibliographical index, which is here and there ren-
dered almost unintelligible through an undue multiplication of
synonyms and the clerical errors which have occasionally crept
into it. But its very compendiousness, which of itself must
have involved a vast amount of labour, may well be allowed
to turn the balance against any shortcomings of the kind
referred to.
I sincerely wish certain errors in the work, of another
kind, could be as easily passed by without further comment.
Unfortunately, for reasons which will develop themselves as
I proceed, they cannot be so. But when they are pointed
out, I venture to think that, from whatever cause they may
have arisen, Prof. Leidy himself will be the first to acknow-
ledge them, quite as much in his own interests as in mine.
Nothing, therefore, of minor import to me personally than
the facts about to be noticed could have induced me to eriti-
cise certain statements made by Prof. Leidy in reference to
my published opinions concerning the freshwater Rhizopods,
im a manner which, although unavoidably adverse, will, I
trust, never appear hostile; more particularly as the United
States Survey Department have done me the great honour
of presenting me with a copy of his magnificent volume.
At page 7 Prof. Leidy makes the following remark :—“ Dr,
Wallich (Annals & Mag. Nat. Hist. 1863, xi. p. 438) divides
the Rhizopods into three orders, the Herpnemata, Protodermata,
and Proteina. In the first are included the Gromide, Fora-
minifera, and Polycystina; in the second the Thalassicollina
and Acanthometrina; and in the third, the Actinophryna,
Lagynida, and Ameebida.”
As already stated, within a couple of years after the issue
of the June 1863 number of the ‘ Annals’ from which the
above paragraph was taken, it was proved by me, not, as
Prof. Leidy observes at p. 279 of his work, “in one in-
stance,’ but in a sufficizntly large number of instances
to place the point at issue beyond dispute, that Gromda nor-
mally possesses both a nucleus and contractile vesicle, and
must therefore, in spite of its ‘ reticularian’’ pseudopodia, be
330 Dr. Wallich on the Rhizopods.
transferred from the lowest to the highest order of the Rhizo-
pods. Had Prof. Leidy read the observations made by me
at a somewhat later period (to which attention has been
already drawn at pp. 822, 323, ante), he would have seen that,
for the important reasons assigned, Gromia had been so
transferred, and would, in all probability, therefore have
accorded the fact as prominent notice as he accorded the state-
ment contained in the paragraph above quoted. But he made
the matter worse by stating at p. 279 of his work, without
any further explanation, that—
“Prof. Schultze intimates the absence of a contractile
vesicle in Gromza ( Arch. f. mikrosk. Anat. 1875, p. 116) ;
but Dr. Wallich remarks that in one instance he detected this
temporary (!) organ in Gromia oviformis:”’ the most un-
intelligible part of the affair being that he should have
stopped short in his quotation of my paper at the very point
where my reasons were given for not deeming it expedient
to speak positively about the presence of the contractile vesicle
in Gromza on the strength of a single observation, and conse-
quently determining to await its confirmation through a sufli-
cient number of further observations.
I repeat, had Prof. Leidy cited the whole of the passage
referred to, he might have been induced to consult two
of my later papers, namely one on “he Affinities of the
Polyeystina’ (mentioned in his Bibliographical list under
my name), which was published in the ‘ Quart. Journ. Microsc.
Science’ for July 1865, and another ‘‘ On the Fundamental
Error of constituting Gromia the type of Foraminiferal
Structure,” published in the ‘ Annals’ for Feb. 1877, and
have thus avoided so obvious a misapprehension of my obser-
vations, and one so calculated to throw unmerited discredit on
the entire basis of my classification.
But so completely did Prof. Leidy misinterpret or over-
look my writings in relation to Gromia, that at p. 277 he
expresses himself as follows, under the head of “ Forami-
nifera :”—‘‘ These, though consituting the most extensive and
important order of the Rhizopods, are almost exclusively
marine. A single well-known genus, Gromia, is represented
by several species inhabiting salt and fresh water ;’’ and in
the page following the last named, ‘The genus is of special
interest Lecause it is a representative, in the simplest condition,
of that great order of Rhizopods, the Foraminifera, which are
exclusively marine with the exception of the present one,
Gromia.” And at pp. 278-279 he says that the body of
Gromia “ contained a large clear or pale granular nucleus situa-
ted centrically or eccentrically, and also variable proportions of
Dr. Wallich on the Rhizopods. Ball
WACHOLES <5, A vacuole was at times observed to gradually
disappear; ..,. but it was doubtful whether any of these corre-
sponded with the contractile vesicle of other Rhizopods.” He
then gives a very good description of the characters of the only
form of Gromda he had met with in North America, named by
him G.terricola, partly on account of its habitat ‘‘ in the crevices
of the pavement in the yard attached to his home in the city of
Philadelphia,” and partly, I presume, owing to the animal
having a habit of accumulating at the posterior portion of its
test “more or less dirt consisting of fine granules and coarse
particles of quartz sand” (p. 280). But beyond this his
description of G. terricola would hold just as good for G. ovi-
jformis, or indeed any of the polymorphous varieties assumed
by these organisms, for it presents no new characters.
The second erroneous statement I have to notice is even
more extraordinary than the former one, inasrauch as it does not
involve a misapprehensionof my written opinions, but attributes
to me statements which are directly opposed to those really
made by me on the points in question. I allude to Prof.
Leidy’s assertion in relation to Diffugia symmetrica and the
entire series of new testaceous forms, of which, with three
before-mentioned exceptions, not one had been previously dis-
covered, so far as I am aware, either in this country or
elsewhere, prior to the appearance of my paper ‘On the
Extent and some of the principal Causes of Structural Varia-
tion among the Difflugian Rhizopods,’ published in the
‘ Annals’ for March 1864.
At pp. 150 and 151 of his work Prof. Leidy says, ‘“ The
series of specimens represented by Dr, Wallich in figs. 27 to
33, pl. xvi. of the 13th vol. ‘Annals & Mag. Nat. History’
for 1864, and described as transition forms of Diflugia sym-
metrica, appear to me to pertain to the same animal as Nebela
collaris.”’
It is not for me to hazard a conjecture how such a distorted
view of my clearly-expressed opinion regarding the tran-
sitional series of forms referred to could have been arrived at
by so careful an observer. At all events, I can positively
affirm that I never entertaimed or expressed such an opinion.
In all I wrote on the new varieties of the Difflugide I referred
only to the outwardly visible characters of the tests for reasons
already stated; and neither directly nor indirectly described
“the specimens represented in my figures 27 to 33 of pl. xvi.,”
as “transition forms of Difflugia symmetrica.” What I did
state was that I considered them all as varieties of Diflugia
proteiformis or its variety D. pyriformis; and as such I
must continue to regard them until some much more satisfac-
332 Dr. Wallich on the Rhizopods.
tory reasons for cancelling my title to priority and superseding
the generic position to which I referred them shall have been
produced than those offered in Prof. Leidy’s volume.
In my observations on the Difflugian Rhizopods, in the
‘Annals’ for March 1864, above referred to, I endeavoured
to show that the entire series of Difflugian tests represented in
my plates are constructed by animals which, with no known
exception, are generically as well as specifically identical.
There is nothing improbable therefore in the assumption that
the entire series in their earliest condition, that is to say
when the chitinoid exudation of which the test is entirely
composed makes its appearance around the sarcoblast, are
identical in form. When we study forms obtained from a
sufficiently wide geographical area we find many previously
existing intervals between varieties bridged over; and if
we note the differences in the external conditions by which
the animals are surrounded, whether of locality or climate,
we are able, generally speaking, to trace some relation be-
tween the peculiarities of the varietal forms and the physical
agencies which have helped to produce them. But in the
cases under notice, neither in the structure nor the degree of
organization of the animal itself, nor in the outward figure of
any of the forms of test, are there any differences to be de-
tected which could distinguish them generically from their
exact prototypes and counterparts in already well-known and
established typical Diffugian forms. For, as I have always
maintained, the changes brought about in the external
characters observable in the tests of the new varieties
described by me in the ‘Annals’ for March 1864, are
purely dependent on contact of the chitinoid bases of the
tests with materials present in the medium by which they
are surrounded, and therefore ought not to be employed for
generic or specific subdivision.
A great deal of additional evidence in the same direction
might be now adduced from my previous writings did space
allow. Before proceeding further I must therefore confine
myself to offering a few brief remarks bearing directly on
what has gone before.
Without the production of any satisfactory reasons for his
statements or for taking such a step as giving a new generic
name to Difflugia symmetricu, which, as he himself admits,
had been first described by me, Prof. Leidy thus defines the
new genus he has created under the name of ‘ QUADRULA:??
—‘ Shell compressed pyriform, transparent, colourless, com-
posed of square plates of chitinoid membrane arranged in
transverse or more or less oblique series, in consecutive or
Dr. Wallich on the Rhizopods. 333
alternating order. Mouth inferior, terminal, oval. SARcODE
COLOURLESS, HAVING CHARACTERS OF THAT OF DiFrLueGrs,
&e.” (op. cit. p. 142).
In describing the species he says :—‘' Quadrula symmetrica,
the only representative of its genus, is remarkable for the
peculiar construction of its shell, which is compressed pyr?-
ARMOR 3. The general arrangement [of the plates] is like
that of tiling with variable regularity. . . . They are not en-
tirely disposed with the symmetry expressed by their name,
for frequently smaller plates break the regular succession
of larger ones, and sometimes one angle of a plate replaces
that of a contiguous one” (op. cit. p. 143). And, again,
“ Quadrula symmetrica was first described” in 1863-64
“by Dr. Wallich, under the name of Diffugia symmetrica,
from specimens found in England. It was more recently ”’
(that is to say in 1875, or just eleven years after I described
and figured it) “described, and referred to a new genus, by Prof.
Schultze from specimens found near Dresden. Ehrenberg
described the same as pertaining to three different species
under the names of Difflugia assulata, D. carolinensis, and
D. leptolepis. ‘These, in 1871 (Abhandl. Akad. Wiss. Berlin,
1871, p. 246), with a number of other forms, he referred to a
subdivision of Diffiugia with the names of Assulina and Holo-
glypha. As, however, the latter would apply to the first mem-
bers of the subdivision indicated, which appear to be only
varieties, or at most two species of Cyphoderia, neither of the
names could be considered as appropriately taking precedence
of Quadrula, distinctly applied to Assulina assulata, the
fourth member of Khrenberg’s list’”’ (of 1871).
As a matter of fact, Diflugia symmetrica is the only aber-
rant member of my series of new testaceous Difflugide which
was not included in the synoptical list given at p. 240 of the
‘Annals’ for March 1864, being then, as it is still, con-
sidered by me to have been sufficiently identified and defined
in any classification having forits end a systematic arrange-
ment based only on natural characters. Moreover, it seems
extraordinary that the established rules of priority and nomen-
celature (to which Prof. Leidy here draws such marked atten-
tion) should, with his sanction, have been infringed by Prof.
Schultze, when the latter writer, in 1875, superseded the
generic name given to the form in question, at the same time
retaining the specific name applied to it by me as distinctly
indicative of its special character.
I venture to assert there is not a single new character
assigned in Prof. Leidy’s definition of the genus “ Quadrula”’
(or, to use an expression of his, Difflugia symmetrica ‘“ under
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 23
334 Mr. A. G. Butler on Lepidoptera from
the name of” “Quadrula symmetrica”) beyond those ad-
duced by me, except one which I undertake to say is erro_
neous, namely that ‘‘the plates are either chitinoid or mem
branous.”” On the other hand, he undoubtedly furnishes the
completest proof of the propriety of referrmg the form to the
genus Diffiugia when the only remark he has te make
upon the animal is that the sarcode ‘has the same character
as that of Difflugia.” This ought to be borne clearly in mind,
for Prof. Leidy subsequently speaks of Quadrula symmetrica
as “‘ the only representative of its genus.”
But it is quite needless to argue the question of priority a
step further, for I now have to place on record an important
fact of which I was ignorant at the time I described Difflugia
symmetrica in 1863-64, and discovered only within the present
year, viz. that this identical form had been figured in Khren-
berg’s ‘Infusionsthierchen’ as a Difflugia. Hhrenberg’s subse-
quent remarks in the ‘ Proceedings of the Berlin Academy’
and elsewhere, to which allusion is now made by Prof. Leidy,
are altogether beside the question at issue, except to the
extent of proving that Ehrenberg recognized the validity of
my specific appellation of “ symmetrica”’ and retained it. Of
course, the moment I found I had overlooked Ehrenberg’s
title to priority (unfortunately too late to be made known te
the illustrious dead), I determined on the first suitable occasion
to cede all title to the discovery of D. symmetrica, though I
was undoubtedly the first to detect it in this country, and to
discover, describe, and figure the other new forms of testa-
ceous Difflugide of which I shall have oceasion to speak in
the concluding part of this paper.
[To be continued. ]
XXXI.—On a Collection of Lepidoptera made at Manipur and
on the Borders of Assam by Dr. George Watt. By ARTHUR
G. BuTuer, F.L.8., F.Z.8., &e.
[Plate VIII. ]
[Concluded from page 310. ]
Lycenide.
69. Cyaniris placida.
Cyaniris placida, Moore, P, Z. 8, 1883, p. 528, pl. xlviil, fig. 5.
Near Assam.
Only males of C. placida were obtained.
Manipur and the Borders of Assam. 335
70. Cyantris puspa.
Polyommatus puspa, Horsfield, Cat. Lep. E. I. Co. p. 67. n. 3 (1828).
6. Near Assam.
Two of the three examples obtained seem a little aberrant,
and may belong to a distinct but allied species; they are,
however, in poor condition, and it is possible that the species
may vary somewhat both in the width of the outer border on
the primaries and in the size and prominence of the markings
on the under surface. I have, however, failed to notice
similar variation (excepting where due to seasonal polymor-
phism, asin the North-American species) in the allied species.
I do not find any characters to warrant the separation of the
other male from Horsfield’s Javan type.
71. Nacaduba ardates.
Lycena ardates, Moore, P.Z.S. 1874, p. 574, pl. lxvii. fig. 1.
Near Assam.
Four damaged males were obtained, no two ot them abso-
lutely alike in the pattern on the under surface of the prima-
ries. A nearly allied “species” described by De Niceville
(Journ. Asiat. Soc. Beng. vol. lii. p. 72, pl. i. fig. 13, 1873) is
separated from the above by its superior size, by the abbrevia-
tion of the band crossing the cell on the under surface, and by
the absence of the lowest spot in the discal series. The speci-
mens before me vary from 22 to 24 millim. in expanse of wing ;
the band is only abbreviated in one of the larger specimens,
and, though all have the full number of sections to the discal
band, the last two sections (they can hardly be called spots) ~
are sometimes in line and sometimes decidedly out of line;
the failure of the last spot of a discal series or the last section
of a discal band is of frequent occurrence in the Lycenide ;
therefore, since both N. ardates and N. bhutea appear to be
common in Sikkim, I feel some doubt as to the validity of
the latter as a distinct species; at the same time, with only
the figure of this form before me I cannot positively assert
that it is not distinct *.
72. Lampides elpis.
Polyommatus elpis, Godart, Enc, Méth. ii. p, 654. n. 125 (1828).
g. Near Assam.
We have this species also from Silhet ; the Indian examples
* T haye, since the above was written, seen one imperfect specimen of
N. bhutea in Mr. Moore’s collection; I should certainly hesitate to de-.
scribe so nearly allied a form myself.
23*
336 Mr. A. G. Butler on Lepidoptera from
are slightly more azure in tint than those from Java, but do
not otherwise differ.
73. Catochrysops lithargyria.
Catochrysops lithargyria, Moore, Ann. & Mag. Nat. Hist. ser. 4,vol. sx-
p- 3840 (1877).
&. Near Assam.
74. Catochrysops strabo.
Hesperia strabo, Fabricius, Ent. Syst. iii. 1, p. 287. m. 101 (1793).
~@. Near Assam.
75. Myrina etolus.
Papilio etolus, Fabricius, Mant. Ins. ii. p. 66. n. 620 (1787).
3S. Manipur.
Papilionide.
Prerin2.
76. Colias Fieldit.
Colias Fieldii, Ménétriés, Cat. Mus. Petrop. Lep. i. p. 79, pl. i. fig. 5.
(1855).
& 2%. Near Assam.
Dr. Watt obtained fifteen examples, the largest of which
measures 64 millim. in expanse of wing, and thus compares
favourably with C. aurorina of Kurope. ‘The smallest example
in the Museum-series is one from the N.W. Provinces of
. India; it not only differs in its greatly reduced size and some-
what more produced primaries, but in its narrower borders,
blackened veins, and pupilled discocellular spot ; possibly it
may be distinct; its expanse of wing is only 36 millim. I
leave the question of the distinctness of these two forms
until further material turns up ; perhaps Mr. Elwes will be able
to decide the matter.
Before passing on to the rext genus (Terdas) I feel called
upon to say somewhat touching Mr. Distant’s recent treat-
ment of the genus (Lep. Malayana, pp. 302-307), which is
based wholly upon the supposition that Mr. Pryer’s experi-
ments with Japanese species were as careful as he himself
thought them. From long experience in plant-growing I
know well that nothing is easier than to overlook such con-
spicuous objects as scale-insects, even though one fancies
one has examined carefully every leaf of a plant; how
much more so the small eggs of Tertas! Mr. Pryer says
Manipur and the Borders of Assam. — 337
that he potted a number of plants, and after looking over
them, or, in his own words, “ carefully examining every leaf
for eggs or larve,” he placed upon them females of Terias
mandarina, and the result was that he bred 7. mandarina
(at which he was greatly astonished, and immediately decided
that this was a seasonal form of another species) ; he also bred
T. Mariesit and some of the intergrades, which seem not to
have astonished him at all.
My. Pryer’s experiments may be satisfactory, or they may
not; if the plants possessed a great number of leaves, the
probability is that some eggs were overlooked ; if they were
roughly potted, it is not improbable that such eggs as were
upon them fell upon the mould and were hatched there ; but
anyhow 7. mandarina cannot be called a seasonal form of
T. Mariesii or T. hecabe, if it produces itself.
Secondly, Mr. Distant expects that breeding will prove 7. sart
to be “ only a variety of 7. hecabe ;” if so, why not expect the
whole of the Old- World species to prove varieties of T. hecabe,
since forms closer to T. hecabe than 7. sar¢ are found in all
parts of Asia, Africa, and Australia? Isit reasonable to sug-
gest that 7. sar7¢, a purély Malayan species, may be a variety
of a species which ranges from Darjiling to the Philippines,
or, at any rate, is at present assumed to do so (for it is doubt-
ful whether all the specimens now referred to T. hecabe are
rightly placed with that species). Mr. Distant remarks that
breeding experiments have not yet proved that 7. sar7 is a
variety of 7. hecabe ; yet Horsjfield, Thwaites, and Mackwood
have all bred it, by his own showing. However I am will-
ing to accept his admission—a rash one for an entomologist
to make—‘‘ I treat this species as a variety” (see p. 321).
I know of many lepidopterists who do this; but Mr. Distant
is the first who has boldly come forward and confessed it.
77. Terias venata?
Terias venata, Moore, Cat. Lep. HE. I. Comp. i. p. 65. n. 117, pl. ii. a.
fir. 2 (1857).
Near Assam.
A pair of a Terias agreeing best with this species, but
apparently distinct; I, however, consider that, as the diffe-
rences are slight, two somewhat imperfect specimens are
insufficient material upon which to separate this form from
T. venata.
78. Terias hecabeotdes.
Terias hecabeoides, Ménétriés, Cat. Mus. Petrop. Lep. i. p. 86, pl. ii,
fig. 2 (1855). :
3. Near Assam.
338 Mr. A. G. Butler on Lepidoptera from
This may eventually prove to be distinct from typical 7.
hecabeoides, the specimens being decidedly larger and more
primrose-coloured than in the figure above quoted, which is
nearer typical 7. hecabe.
79. Terias heliophila,sp.n. (Pl. VIII. fig. 2.)
&. Bright primrose-yellow : primaries above with a broad
dark brown external border nearly as in 7. sart, but with the
sinus distinctly bisinuated; external border of secondaries mode-
rately. broad, a little less so than in typical 7. Mariesiz, with
distinctly sinuated inner edge: under surface bright gamboge-
yellow, with markings of 7. wsdope, only less strongly defined ;
the apical streak of the primaries represented by two or three
diffused red-brown spots. Expanse of wings 47 millim.
Near Assam.
Three male examples were obtained, but only one of
them is in tolerable condition ; the species, however, cannot
be referred to anything hitherto described, its nearest ally
being 7. maroensis from Timor-Laut.
80. Tertas stmulata.
Terias simulata, Moore, Lep. Ins. Ceylon, i. p. 119, pl. xlv. figs. 2, 2
31 Assi), a, Moore, Lep. Ins. Ceylon, 1. p. 119, pl. xiv. figs. 2, 2 a,
Near Assam.
Five examples, in somewhat worn condition.
81. Terias esiope.
Terias esiope, Ménétriés, Cat. Mus. Petrop. Lep. i. p. 85, pl. ii. fig. 8
(1855).
&o ¢. Near Assam.
Nine worn specimens were obtained.
82. Terias wrregularis.
Terias irregularis, Moore, P. Z.S. 1882, p. 253, pl. xii. fig. 3.
3. Near Assam.
83. Dercas Verhuelliz.
Colias Verhuelliz, Van der Hoeven, Tijd. Nat. Gesch. v. pl. viii. figs. 3, 4
(1838).
3 2. Manipur.
Only one pair was obtained.
84. Lxtas evippe.
Papilio evippe, Drury, Ill. Exot. Ent. i. pl. v. fig. 2 (1778).
Ten males. Manipur.
Manipur and the Borders of Assam. 339
85. Hebomoia glaucippe.
Papilio giaucippe, Linnzeus, Mus. Lud. Ul. p. 240 (1764).
S- Manipur.
86. Prioneris thestylis.
Pieris thestylis, Gray, Zool. Miscell. p. 76 (1842).
Manipur.
Seven males were caught, two of them not quite typical,
the yellow angular belt on under surface being wider than
usual. We have a similar example from Darjiling in the
Museum series.
87. Delias tthiela.
Thyca ithiela, Butler, Ann. & Mag. Nat. Hist. ser. 4, vol. iv. p. 242
(1869).
g&. Near Assam.
Originally described from Penang, and on that account
included by Mr. Distant in his admirable work ‘ Rhopalocera
Malayana;’ this locality, however, was an error arising out
of the fact that the type was labelled thus—‘ P.,’ which, with
Wallace’s specimens, stands for “ Penang ;” but with speci-
mens received from the East India Company (as Mr. Moore
pointed out some two or three years since on a ticket which
he attached to this very species) it stands for ‘ Darjeeling,
Pearson.” Had Mr. Distant examined my type, which, by
his own admission, he did not do, he would have avoided the
repetition ef this error.
88. Delias agostina.
Pieris agestina, Hewitson, Ex. Butt. i. Pieris, pl.i. figs. 1, 2 (1852).
G. Near Assam.
89. Appias galba.
Tachyris galba, Wallace, Trans. Ent, Soc. ser. 3, vol. iv. p. 378, n. 41
(1867).
Manipur.
Seven examples were obtained.
90. Appias Eleonora.
Pieris Eleonora, Boisduval, Sp. Gén. Lep. i. p. 481. n. 64 (1836).
3 2. Manipur.
Out of twenty-four examples only one is a female.
91. Appias vacans.
Appias vacans, Butler, Trans. Ent. Soc, 1879, p. 490.
3. Manipur.
340 Mr. A. G. Butler on Lepidoptera from
Five males, agreeing exactly with typical A. vacans in the
more sulphur-tinted colour of the under surface, by which
character alone can I distinguish the males of this species
from those of A. Hleonora, whereas the females differ widely
enough. Mr. Moore’s figure in ‘ Lep. Ceylon’ better repre-
sents A. Eleonora, being decidedly too ochraceous for my
male of A. vacans.
92. Hiposcritia durvasa.
Pieris durvasa, Moore, Cat. Lep. E. I. Comp. i. p. 73. n. 142 (1857) ;
P.Z.8. 1857, pl. xliv. fig. 6.
Four males. Near Assam.
93. Hiposcritia lalage.
Pieris lalage, Gray, Zool. Miscell. p. 76 (1842) ; Doubleday & Hewitson,
Gen. Diurn. Lepid. pl. vi. fig. 5 (1847).
Ten males. Manipur.
94, Hiposcritia pseudolalage.
&. Catophaga pseudolalage, Moore, P. Z.S. 1879, p. 142.
Manipur.
Three males represent this species, but in so shattered a
condition that they are chiefly valuable as indicating the
existence of the species at Manipur.
95. Hiposcritia argyridina, sp. n.
¢. Above similar to H. pseudolalage, but usually smaller
and with the spot on second median interspace better sepa-
rated from the external border ; basal area more silvery than
in any of the allied species : below it differs in the apical area of
primaries, and whole of secondaries being irrorated with brown,
as in H. mahana, instead of pale buff. LExpanse of wings
56-62 millim.
“ January 8,1881. Valley of the Khéonah Khong, Eastern
Ranges, Manipur.
‘‘] was surprised on reaching the river to find a white
butterfly in great abundance flying down the stream in
strings of fifty to a hundred like ducks. I had a swing
with my net and caught ten to fifteen at each turn. I don’t
yemember to have seen this habit, nor indeed the insect before.
Not a single specimen was seen flying up the river, nor
one fluttering about; all seemed intent upon some definite
journey down stream, each following his neighbour: if dis- —
turbed they changed their course for a time, but soon re-
sumed it. I was still further surprised to find the same insect
Manipur and the Borders of Assam. 341
in the woods adjoining, stngly, loitering, but flying, upon the
whole, up the valley.” —Dr. Waitt.
The female is in Mr. Moore’s collection as that sex of Z.
pseudolalage; the latter, however, is much more like IZ. lalage
on both surfaces; it is, however, smaller, has the anal half
of the external border of secondaries partly divided by a
submarginal macular grey streak, and on the under surtace
the basal area of these wings and the disco-submarginal dark
grey line are far better defined. We have it from Darjiling,
whence also all our male examples were received.
Dr. Watt sent home seventeen specimens of H. argyridina,
but unfortunately the bulk of them were more or less damaged,
probably having knocked one another about in the net. It is
a significant fact that no other species was mixed up with
them ; had there been, it would have cast a doubt on the
validity of the species in this group.
96. Hiposcritia shiva.
Liposcritia shiva, Swinhoe, P.Z,S. 1885, p. 138. n. 106, pl. ix. figs. 1, 2.
Manipur.
Twenty-six examples were collected. Colonel Swinhoe
says that it is ‘very much like a diminutive ZH. narendra
above ;” but the greater part of the specimens before me are
quite as large and some even larger than that species; it
varies in expanse of wing from 47 to 68 millim.; it varies
also in pattern not a little, in the number and size of the
white subapical spots on the primaries, in the prominence or
entire absence of the black process of the external border
on the second median interspace, in the absence or prominence
of the colouring and marking of the under surface, most
examples being almost as yellow as H. durvasa and with
similar markings to those of H. narendra; nevertheless it
perfectly holds its own as a distinct species.
97. Hiposcritia mahana.
3. Appias mahana, Moore, Aun. & Mag. Nat. Hist. ser. 4, vol. xx. p. 48
(1877).
Wallace (Trans. Ent. Soc. 3rd ser. vol. iv. p. 382) speaks
of this species, under a MS. name of Boisduval’s, as appa-
rently undescribed, and says that the name “ should be alto-
gether dropped ;” he appears, however, not to have described
the species. ‘The latter is similar on the upper surface to H.
shiva, but its female more nearly resembles that sex of H.
indra, differing from it chiefly in its smaller size, less pro-
duced primaries, the complete submarginal series of white
842 Mr. A. G. Butler on Lepidoptera from
spots on upper surface of secondaries, and the more dusky
colouring of these wings on the under surface; the male
differs on the under surface from H. shiva in the brownish
irrorated character of the apical area of the primaries and
whole of secondaries on the under surface, in which respect it
corresponds with H. pandione. Hxpanse of wings, ¢ 59-
65 millim., ? 68 millim.
One male. Manipur.
H. mahana is in the. Museum collection from Silhet and
Calcutta.
98. Huphina nama.
Pieris nama, Moore, Cat. Lep. E. I. Comp. i. p.76. n. 148 (1857);
P.Z. 8. 1857, pl. xliv. figs. 1, 2.
Twelve males. Manipur.
99. Huphina phryne.
Papilio phryne, Fabricius, Syst. Ent. p. 473, n. 131 (1775).
&. Near Assam.
100. Ganoris gliciria.
Papilio gliciria, Cramer, Pap. Exot. 11, pl. clxxi. EH, F (1779).
6 o.) inane River, Deces133ir
Dr. Watt collected twenty-five examples of this species.
101. Ganoris ajaca.
Pieris ajaca, Moore, P. Z. 8, 1865, p. 490, n. 21, pl. xxxi. fig. 16.
3 9. Near Assam.
One pair only was obtained, both examples being a little
larger than Moore’s type, but not otherwise differing.
PaPiILioninaA.
102. Papilio antiphates.
Papilio antiphates, Cramer, Pap. Exot. i. pl. xxii. A, B (1779).
Two examples. Manipur.
103. Papilio doson.
Papilio doson, Felder, Verh. zool.-botan. Gesellsch. xiv. p. 805. n. 222
(1864).
One example. Manipur.
104. Papilio acheron.
Zetides acheron, Moore, Ann. & Mag. Nat. Hist. vol. xvi. p. 120 (Aug.
1885).
Hight examples. Manipur.
Manipur and the Borders of Assam. 343
105. Papilio bathycles.
Papilio bathycles, Zinken, Nova Acta Acad. Nat. Cur. xv. p. 157, pl. xiv.
figs. 6,7 (1831).
Seven specimens. Near Assam.
106. Papilio sarpedon.
Papilio sarpedon, Linneeus, Mus. Lud. Ulr. p. 196 (1764).
Six more or less worn examples. Manipur.
107. Papilio agamemnon.
Papilio agamemnon, Linnzeus, Mus. Lud. Ulr. p. 202 (1764)
Manipur.
Three examples were obtained.
108. Papilio xenocles.
Papilio xenocles, Gray, Zool, Miscell. p. 74 (1842).
Manipur.
Four examples were taken.
109. Papilio danisepa, sp. n.
Allied to P. caunus, and mimicking D. rhadamanthus ; it
differs from the Bornean P. cawnus in its superior size, the
much longer costal margin of the primaries, the much
larger white patch at the end of the cell, the better defined
submarginal spots on the primaries, less numerous and smaller
submarginal spots on the secondaries, and in having the basal
half of the secondaries white crossed by black veins, Ex-
panse of wings 120 millim.
One male. Near Assam.
In the Museum collection we have a male scarcely differing
from the above, and evidently of the same species, from
Silhet. In the Hewitson collection is a male from Borneo
corresponding with our Bornean specimen ; there are also two
males from Sumatra differing from the latter much as Dani-
sepa diocletianus does from D. Lowi; they agree with P.
caunus in form of wing and are of about the same size, but
differ in having nearly twice as much white at the base of
the secondaries*. As there can be no reasonable doubt of
their being constant to locality, I propose to name the Suma-
tran race P. velutinus. I have no doubt that the P. caunus
of M. Oberthiir’s list, from Java, is a fourth form in which
the basal white patch has almost disappeared, whilst that from
Nias should have no patch at all.
* P. egialus, Distant (Annals, vol. xii. p. 352), from Singapore, seems
to differ in having much less white at base. ;
544 Mr. A. G. Butler on Lepidoptera from
110. Papilio helenus.
Papilio helenus, Linneeus, Mus. Lud. Ulr. p. 185 (1764).
so. Near Assam.
111. Papilio ganesa.
Papilio ganesa, Gray, Zool. Miscell. p, 73 (1842).
(Three specimens.) Near Assam.
112. Papilio paris.
Papilio paris, Linneus, Mus. Lud. Ulr. p. 184 (1764).
3g. Near Assam.
113. Papilio cacharensis, sp. n.
Smaller and narrower in the wing than P. Doubledayiz, to
which it is most nearly allied; the white patch in the cell of
secondaries much smaller, only occupying about two fifths
instead of two thirds of the discoidal areole, the other white
spots also smaller. Hxpanse of wings 99-108 millim.
One male. Near Assam. :
Tn the Museum collection we have two females from Cachar.
P. Doubledayti expands from 116 to 136 millim.
Hesperiidae.
114. Astictopterus diocles.
Nisoniades diocles, Moore, P. Z.S. 1865, p. 787.
Near Assam.
Sphingide.
115. Protoparce orientalis.
Protoparce orientalis, Butler, Trans. Zool. Soc. vol. ix. p. 609, pl. xci.
figs. 16, 17 (1876).
¢. Manipur.
Agaristide.
116. Husemia bellatrix.
Eusemia bellatrix, Westwood, Cab. Orient. Ent. pl. xxxiii. fig. 2.
Near Assam.
Chalcosiide.
117. Amesita aliris.
Gynautocera aliris, Doubleday, Ann. & Mag. Nat. Hist. ser. 1, vol. xix.
p- 74 (1847).
Manipur.
Manipur and the Borders of Assam. 345
CALLAMESIA, gen. nov.
Allied to Amesia, but the primaries of a more triangular
(Zuplea-like) form ; the first subcostal branch running into
the costal vein instead of running freely to the margin, both
first and second branches emitted much further from the end
of the cell, third and fourth branches forming a much narrower
fork to apex; upper radial nearly straight instead of curved ;
lower radial emitted from the posterior angle of the cell instead
of from the third median branch ; submedian and internal
veins united beyond the middle by a transverse veinlet* ;
secondaries much more oval than in Amesia, but with similar
neuration. Antenne pectinated in both sexes; palpi por-
rected; legs more slender than in Amesia; genitalia of males
not covered by the great horny incised shield common to
Amesia. Type C. midama.
118. Callamesia midama.
3. Epyrgis midama, Herrich-Schiffer, Auss. Schmett. fig. 7.
é. Near Assam.
119. Erasmia pulchella.
Erasmia pulchella, Hope, Trans. Linn, Soc. xviii. p. 446, pl. xxxi.
fig. 5.
Near Assam.
Nyctemeride ?
120. Pterothysanus laticilia.
Pterothysanus laticilia, Walker, Cat. Lep. Het. ii. p. 401 (1854).
Near Assam.
Herr Buchecker thinks that this genus should be placed
(with its near ally Caloschemia) next to Epicopeia, on account
of its having no internal vein to the secondaries; it, how-
ever, differs from Hpicopera in having four branches to the
median vein in all the wings, a radial vein being emitted from
the inferior angle of the cell in each instance ; this is also the
case with Deilemera, Pitasila, Trypheromera, Leptosoma, and
other genera of Nyctemeride. ‘Though it is impossible,
without knowing the earlier stages of a genus like this, to
come to any final decision as to its proper location, it appears
to me that one character of venation should be of equal im-
portance with another. In all probability the internal vein
is merely aborted.
* This very aberrant character, pointed out to me by Herr Buchecker,
first satisfied me that two genera were confounded under Amesia.
346 Lepidoptera from Manipur and the Borders of Assam.
121. Pterothysanus atratus, sp.n. (Pl. VIII. fig. 3.)
Primaries above smoky brown; a large spot near the base
of interno-median area; a second larger spot within the end
of the cell, two small spots beyond the cell; two spots, well
separated, beyond the middle of the costal border; an oblique
subapical ;-shaped marking, a spot at outer third of second
median interspace, and a large excised patch crossed by the
first and second median branches, ail white; a marginal series
of irregular angular pink spots: secondaries white; base,
costal margin, an irregular angulated band, widest at inner
margin, crossing the wing before the middle, and the external
third (the inner edge of which is acutely incised and undu-
lated) smoky brown; five rather small submarginal white
spots; a marginal series of irregular angular pink spots.
Body orange-ochreous, spotted with black ; venter black, with
two parallel series of small white spots. Hxpanse of wings
74 millim.
Near Assam.
Apart from differences of pattern this species is readily
separable from P. laticilia by the pink marginal spots, in
which respect it shows some relationship to P. pictus.
Lasiocampide.
122. Spalyria testacea. .
Dreata testacea, Walker, Cat. Lep. Het. iv. p. 906. n. 9 (1855).
Eupterote testacea, Butler, Ill. Typ. Lep. Het. v. p. 67, pl. xevii. fig. 1
(1881).
Near Assam.
123. Hupterote lucia, sp.n. (Pl. VIII. fig. 4.)
9. Nearest to H. amena from Java; of about the size of
the largest specimens of that species; of a more brilliant
chrome-yellow colour; all the wings crossed by three central
or nearly central purplish-brown lines, dentate-sinuate on the
primaries and zigzag on the secondaries, the third line partly
bounded externally by a nearly straight band of the same
colour, followed at a short distance by a series of dots on the
veins, which towards costa of primaries are united by an
undulated brown line, forming the inner edge of three imper-
fect confluent rings, the lower two of which enclose brown
spots ; the outer edge of the rings commences as an ill-defined
sinuated submarginal line; costa of primaries irrorated with
brown towards apex; markings below less perfect, but
widening towards costa of primaries, chocolate-coloured.
EXxpanse of wings 95 millim.
Near Assam.
On Sponges from South Australia. 347
Readily distinguished from all females of H. amena by the
entire absence of the purplish-rufous undulated bands on the
basal area, of the black spots across the disk, and of the mar-
ginal suffusion.
Euschemide.
124, Huschema excubitor.
Euschema excubitor, Moore, P. Z. S, 1878, p. 846.
Near Assam.
125. Huschema militaris.
Phalena Attacus militaris, Linneeus, Syst. Nat. u. p. 811. n. 12.
Near Assam,
Phyllodide.
126. Lygniodes hypoleuca.
Lygniodes hypoleuca, Guénée, Noct. iii. p. 125, n. 1500.
Near Assam.
Hypopyride.
127. Spirama retorta.
Phalena- Noctua retorta, Cramer, Pap. Exot. ii, p. 29, pl. cxvi. F
(1779).
9. Near Assam.
Of the moths in this collection only one specimen of each
species was captured.
EXPLANATION OF PLATE VIII.
Fig. 1. Prothoé regalhs.
Lig. 2. Terias hehophila.
fig. 3. Pterothysanus atratus,
Fig. 4. Eupterote lucia.
XX XII.—Deseriptions of Sponges from the Neighbourhood of
fort Phillip Heads, South Australia, continued. By H. J.
CaRTER, F.R.S. Ke.
[Continued from p. 294.]
Family 2. Axinellida.
Group 6. MULTIFORMIA.
We now come to the second family of the EcHINoNEMA,
viz. the Axinellida, whose diagnosis, as above extended,
would stand thus :—
348 Mr. H. Tr . Carter on
“« Hichinated with proper spicules projecting from the znterzor
of the fibre. Structure increasing m density dnwards, or
towards the first-formed parts, ¢. e. the axis.” And applying
the same remarks to this group as to the Pluriformia in the
first family, I would observe, with reference to the sponges
mentioned in the ‘‘ key” to my Classification (op. et l. cit.
p- 196), that the caulescent branched species termed by
Schmidt “ Aainella verrucosa” (Spongien Adriat. Meeres,
Taf. vi. fig. 3), but of course without the parasitic polyp,
might form the type of a group named “ Axinellina,” in
which all the species of the genus “ Avinella” that Schmidt
has described (op. czt.) might be inserted, together with others
from Mr. Wilson’s collection, which will be mentioned here- -
after, in most of which the branched caulescent characters
being more marked will afford a still better typical illustration.
Here also might be inserted Dictyocylindrus rugosus, Bk., and
not “ hispidus,” as stated in the “key” to my Classifica-
tion (J. ¢.), since the latter has a spinous club-shaped, echina-
ting spicule and the former has not (see Bowerbank, Mon.
Brit. Spong. vol. ii. pls. xvu. and xx. figs. 1,1, respectively) 5
thus Schmidt has stated of D. rugosus that it has “ das
Ansehen von Axinella cannabina” (op. cit. I. Suppl. p. 15).
The only difference between most of the arborescent Dic-
tyocylindrina and the Axinellina is the presence of the
echinating spicule in the former and its absence in the latter.
Again, Acanthella, Sdt., might also come in here under a
group named “ Acanthellina,” of which the finest specimen
that I have seen is among Mr. Wilson’s dried sponges from
the south coast of Australia, presented to the British Museum
through myself in 1884, now bearing the register no. “84.
10. 10. 2,” and described at length in the ‘ Annals’ of 1885
(vol. xv. p. 114); while Halichondria ventilabrum, Johnst.,
= Phakellia ventilabrum, Bk., of which I have described a
branched form in the ‘Annals’ of 1883 (vol. xu. pp. 316
and 318) under the name of P. ramosa, might be relegated
to a group called “ Phakellina.”
To thesealso might be added two other groupsof more or less
caulescent, brauched, stipitate forms, with hirsute or ragged
surfaces, under the names of “ Phycopsina” and “ Ptilo-
caulina,” for the typical species respectively of Phycopsis
fruticulosa and Piilocaulis gracilis, described for this purpose
in the ‘Annals’ of 1883 (vol. xii. pp. 8319 and 321); if the
former has not been based upon washed-out beach specimens,
which I begin now to doubt, for one can never be certain of
the original form of such contributions: also massive forms,
under the generic name of “ Leucophleus” (tb. p. 823), of
Sponges from South Australia. 349
which a group might be created under the name of “ Leuco-
phlceina ”—each of which has been aduvisedly selected as re-
spectively typical of some of the groups which it has appeared
to me, after my experience with the specimens in the British
Museum, to be most desirable to record at once, or as soon as
[had the time. Doubtless there are many others, but non
possumus.
Looking over my notes and sketches of Multiformia in the
British Museum when my Classification was made (for [I still
possess the MS. volumes in which illustrated descriptions of
all the species and most of the specimens in the collection
were recorded), I find that by far the greater part are branched
and stipitate, some flabelliform, a few vasiform, and still fewer
massive. The branched forms, again, may be shrubby with
the branches cylindrical, dichotomously divided, and smooth
like those of Awinella verrucosa, in which they very much
resemble a digitate Chalina ; or they may be cylindrical and
ragged, ¢.e. proliferously processed all round as in Ptilo-
caulis gracilis ; or rough and shaggy asin Phycopsis hirsuta ;
or the caulescent branches may be compressed and arranged
side by side flabelliformly, that is dichotomously dividing on
the same plane, when, by interuniting and throwing out a
thorny growth from the surface on both sides, with sarcode
tympanizing the intervals, the Acanthelline form may be pro-
duced, or by growing together erect and laterally united into
a group massively, they may assume the form of Leucophleus
massalis. But, as [ have before stated, there appears to me
to be no limit to the varieties of form which the sponges in
every order may assume, and the same forms in every order
which, so long as they were indiscriminately mixed together
under the universal name ‘ Spongia,’’ as in Lamarck’s
‘ Histoire Naturelle des Animaux sans Vertébres,’ was com-
paratively an easy matter; but since a minute examination of
their structure and spiculation under the microscope has neces-
sitated their separation by an almost individual nomenclature,
that which was an ‘easy matter” under a universal term
has become most perplexing. Hence, as one series of forms
does for the whole class, | have-given a tabulated view of these
in the ‘ Annals’ of 1875 (vol. xvi. p. 7, pl. iii.), to which
I must refer the reader for further information on this subject.
As regards the last group of the Axinellide, viz. the
Durissima, I can state no more than at the time I made it,
which I did chiefly for such species as had a very rigid skele-
ton, in which the fibre was very thick and the dried sarcode
hung about it, more or less tympanizing the interstices of the
Ann. & Mag. N. Hist. Ser. 5. Vol, xvi. 24
350 Mr. H. J. Carter on
reticulation like dry glue, scantily cored with thin acerate
spicules, but denuded of everything else, apparently from
long washing in the waves of the beach off which they had
been gathered for preservation—characters which sufficed for
my Catalogue of the specimens in the British Museum, but
are of no practical utility for general purposes; hence, I cannot
insist upon its being retained under any other circumstances.
There were only three of these specimens, and unless future
observation of them in an unmutilated and fresh state should ©
justify their separation from the rest of the Multiformia, the
group ‘‘ Durissima” had better be abolished.
Fam. 3. Pseudoechinonemida, new fam.
Lastly, it becomes necessary to add this third family to
the order HCHINONEMA for the Areniferous species, as pointed
out under the head of “ fam. Pseudohireinida”’ in ‘ Annals,’
1885, vol. xv. p. 319, where my reasons for so doing have
been given at length, so I need not repeat them here.
As an illustration of this family I will at once briefly state
the characters of the fragment in my possession, to which
allusion has already been made in the “ Obs.” to Echino-
clathria favus, before going to the species in Mr. Wilson’s
collection.
Echinoclathria favus, var. arenifera, n. var.
Fragment cylindrical, round at the free extremity, where
there is a contracted, circular, cloacal aperture corresponding
with the hollow imterior; broken off at the other end.
Identical in structure and spiculation with the species
LEichinoclathria favus. Consistence fragile, friable. Colour
now, in its dry state, grey-brown, sand-like. Fibre cored
with foreign objects in addition to its natural spiculation,
together with arenaceous fibre alone; many more foreign
objects adhering to the outside of the fibre than are situated
in its interior. Size of fragment 10 in. long by about 2 in. in
diameter; cloacal canal about 2 in. in diameter.
Hab. Marine.
Loc. Unknown. ? South coast of Australia.
Obs. This variety of Hchinoclathria favus seems to have
been occasioned by its having grown in the midst of sand,
which, as just stated, seems to be much more plentiful in and
around the outside of the fibre than in its interior.
Our Classification so far therefore would now stand thus :—
Sponges from South Australia. 351
Order V. ECHINONEMA. —
Families. Groups.
1. Pluriformia.
a. Ectyonina.
_ 6, KEchinonematina.
e. Dictyocylindrina.
Le JEG rare { 2. Plumohalichondrina.
3. Microcionina.
4, Kehinoclathrina*.
| 5. Baculifera.
. 6. Higoinsina (new group).
(7. Multiformia.
a. Axinellina. -
6. Phakellina.
Os 2a SUG Oi ee 4 c. Acanthellina.
d. Phycopsina.
e. Ptilocaulina.
{| ff. Leucophleeina.
3. Pseudoechinonemida (new a. Echinonematina arenacea.
family). 6, Plumohalichondrina arenacea.
Having premised the revision of my Order V., viz. ECHINO-
NEMA, which time and experience up to now show to me to be
desirable, I will describe the sponges which Mr. Wilson has
kindly sent to me, under the groups to which they seem
respectively to belong, briefly, itis true, but sufficiently for our
present purpose. In this description it should be understood
that we are concerned now with these specimens alone, and
therefore that, where there are no representatives of any of the
groups mentioned in the Table last given (as, for instance,
the Ectyonina or Hetyones), this must be inferred, as it will
not be further noticed.
As all the specimens come from the sea in the neighbour-
hood of “ Port Phillip Heads,” Victoria colony, south coast
of Australia, the “depth” alone will be inserted. Again,
the granulations on the surface, which are respectively com-
posed of tufts of the spicules of the species that thus terminate
the ends of the fibre and are often hispid, frequently serve to
distinguish the HKcHINONEMA from the RHAPHIDONEMA,
which, on the other hand, from their spicules being for the
most part confined to the fibre, do not present this echinated
appearance. ‘The pores, too, which are situated in the dermal
‘membrane between the “ tufts,” are often unnoticed because
not often seen, although they may always be inferred to exist
in the position mentioned.
All the measurements of the spicules are given in 6000ths
* Hehinoclathrata has been changed to Echinoclathrina for uniformity
only.
24*
352 Mr. H. J. Carter on
of an inch (the value of that division of my micrometer-eye-
piece) for comparison, and they are intended to represent the
greatest dimensions longitudinally and transversely of the
average largest kinds approximately, as they very often vary
in this respect, not only in different specimens but in different
parts of the same specimen. When spined or differently
formed from the common type of both acerates and acuates,
this will be mentioned.
Fam. 1. Ectyonida.
Group 1d. HCHINONEMATINA.
1. Echinonema flabelliformis.
Stipitate flabelliform, like a clam-shell in general shape,
moderately thin, stem short. Consistence firm. Colour,
when fresh, ‘pale terra cotta,” now brown. Surface even,
smooth, consisting of a minutely reticulated dermis spread
over areticulated, cancellous, fibrous structure beneath. Pores
in the interstices of the reticulation. Vents in the margin
corresponding to the terminations of branched, radiating,
linear depressions on the surface, which originate towards
the stem. Spicules of three forms, viz. :—1, skeletal, acuate,
55 by 1-6000th in.; 2, echinating, clavate, spined through-
out, 12 by 1-6000th in. including the spines; 3, a small
acuate in tufts confined to the surface, 25 by 3-6000th in.
Structure uniformly compact throughout, hardening generally
towards the stem, but not axially in any part. Size of
specimen 6x6 x $ in.
Depth 19 fath.
2. Echinonema ceespitosa.
Massive, sessile, spreading, with irregular proliferous cauli-
flower surface ; proliferous portions rising above the common
level into most irregular and jagged processes, great and
small, of variable size. Consistence firm, resilient. Colour,
when fresh, “‘ brick-red,”” now sponge-colour. Surface uni-
formly granulated, supporting a smooth dermis. Vents on
the lobular projections. Spicules of three forms, viz. :—1,
skeletal, acerate, cylindrical, nearly straight, almost immea-
surably thin, chiefly confined to the fibre, 45-6000ths long ;
2, echinating, acuate, spined throughout, 20-6000ths long;
3, flesh-spicule equianchorate, naviculiform, bent upon itself,
34-6000ths in. long. Structure columnar, compact, radiating
upwards. Size of specimen, 1} in. high by 5x4 in. hori-
zontally.
Depth 19 fath.
Sponges from South Australia. 353
3. Echinonema pectiniformis.
Flabelliform, circular, stipitate ; margin almost even ; stem
short ; proliferous processes at the base. Consistence hard,
compact. Colour, when fresh, “ pale terra-cotta red ;” now
the same internally, but dermis pale brown. Surface even,
here and there presenting small elevations. Vents on the
elevations, also indicated although not actually seen, on the
margin, by branched depressions marking the course of sub-
jacent excretory canals running towards it. Spicules of two
forms, viz.:—1, skeletal, acuate, 60 by 1-6000th; 2, echi-
nating, clavate, spined throughout, 9 by 1-6000th. Structure
uniformly compact. Ovigerous. Size of specimen 8 by 7 in.,
thickness } in.
Depth 20 fath.
Obs. This and E. flabelliformis appear to be the same
Species.
4, Echinonema tincrustans.
Massive, incrusting, thick, covering the whole of a Pecten.
Consistence firm, resilient. Colour, when fresh, “ brick-
red,” nowrich orange. Surface uniformly granulated. Pores
not seen. Vents numerous, large, scattered over the surface.
Spicules of three forms, viz.:—1, skeletal, slightly fusiform,
abruptly pointed, chiefly in the fibre, 105 by 14-6000th ; 2,
echinating, acuate, clavate, spined throughout, 18-6000ths
long ; 3, flesh-spicule, equianchorate, naviculiform, 4-6000ths
long. Structure compact, sarcode orange-yellow. Size of
specimen 2 x 34 in., 2 in. thick.
Depth 11 fath.
Group 1c. DICTYOCYLINDRINA.
5. Dictyocylindrus pinnatifidus.
Stipitate, compressed, bunch of cylindrical stalks of various
lengths, often divided polychotomously as well as dichoto-
mously, terminating in long and short lengths and in sharp
points which are sometimes bifid, proliferously plumose or pin-
nate in two lines opposite each other, feather-like, for some
distance up the branch. Consistence soft, hirsute or velvety
on the surface. Colour, when fresh, ‘dark brown,” the
same now. Surface uniformly granulated, hispid, the latter
more particularly where the dermis has been abraded.
Pores and vents not conspicuous. Spicules of three forms,
viz. :—1, skeletal, long, setaceous, acuate, 255 by 3-6000ths ;
2, subskeletal, acuate, smooth, averaging 75-6000ths long;
354 _- Mr. H: J. Carter on
3, echinating, acuate, clavate, spined throughout, 17-6000ths
long. All congregated together and when projecting from the
superficial ends of the fibre producing the granulations and
hirsute character of the surface. No. 2, in great abundance,
separate or together leaf-like, round the lower part of no. 1.
Structure soft and hirsute on the surface, hard towards the axis,
very like Aainella setacea (p. 359), which, but for the absence of
the echinating spicule (which, however, is often soscarce in this
kind of sponges as to pass unnoticed without prolonged exa-
mination), would have been placed in the group Dictyocylin-
drina. Size of specimen 12 in. long.
Depth 5 fath.
_ Obs. By “ compressed” is meant more or less in the same
plane. .
6. Dictyocylindrus cacticutis.
Stipitate, somewhat compressed head of branches inter-
united after the first division into irregular compressed lobes,
proliferously covered with radiating, ragged, thorn-like ridges
and points. Consistence soft on the surface, harder towards
the axis. Colour, when fresh, “ black,’ now black-brown.
Surface scattered over with thorn-like elevations, cactus-like,
covered by a smooth dermis. Vents chiefly on the margins of
the compressed lobes. _Spicules of two forms, viz. :—1, skele-
ial, subpinlike, curved, smooth, 65 by 2'-6000ths, chiefly
confined to the fibre; 2, echinating, acuate, spined, 25 by
3-6000ths, including the spines. Structure compact, chiefly
towards the axis, but not distinctly hard in the centre. Size
of specimen 6 x 3X38 in, including the stem, which is short
and thick.
Depth 19 fath.
7. Dictyocylindrus piniformis.
Stipitate, massive head of proliferous lobes; lobes com-
pressed, thick, expanded, united together in the centre ; irre-
eularly and reticulately nodose over the surface and margins.
Consistence resilient externally, becoming dense towards the
axis. Colour, when fresh, “drab,” now sponge-drab. Pores
and vents not conspicuous. Spicules of three forms, viz. :—
1, skeletal, acerate, curved, smooth; 2, also skeletal, but
acuate, curved, and smooth, both about the same size, viz. 35
by 4-6000th; 3, echinating, acuate, clavate, spined through-
out, 12-6000ths long. Structure compact externally, becom-
ing denser towards the axis. Size of specimen o in. high
including the stem, head 3x 3 in. horizontally.
Depth not stated.
Sponges from South Australia. 305
Group 2, PLUMOHALICHONDRINA.
8. Plumohalichondria mammillata.
- Massive, sessile, with mammilliform erect lobes. Consis-
tence soft, resilient when wet, hard when dry. Colour, when
fresh, ‘‘ venetian red,” the same now inside, but paling to-
wards the dermis. Surface even, uniformly but largely granu-
lated; dermis reticulated over the granulations or elevated
parts. Vents large, scattered irregularly over the mass, none
at the ends of the mammilliform lobes. Spicules of four
forms, viz.:—1, skeletal, acuate, curved, spined generally,
about 35 by 1-6000th; 2, the “ tibiella,”’ acerate, almost
straight, slightly fusiform and abruptly pointed, about 44 by
2-6000th ; 3, echinating, smaller, acuate, spined all over, 12-
6000ths long ; 4, flesh-spicule, equianchorate, angulate, 43-
6000ths long. ‘The tibiella is chiefly confined to the axis of
the fibre. Nos. 1 and 3 echinating, and no. 4 confined to the
sarcode. Structure open resilient, soft geuerally, no axial
condensation. Size of specimen 5 in. high, 6 x 3 in. horizon-
tally.
Depth 3 fath.
Obs. Very like the British species, viz. Plumohalichondria
plumosa= Hymeniacidon plumosa, Bk. (Mon. Brit. Spong.
vol. 1. p. 195), and Microciona plumosa, Bk. (ib. vol. in.
pl. xxiv. fig. 7, &c.), but different from the Cape species,
wherein the large spinous acuate is mixed up with the tibiella
in the axis of the fibre. The Cape species, which might be
termed ‘‘P. capensis,” is the finest of all that I have seen, and
as yet has been undescribed, although it appears to be as
abundant as it is remarkably fine. There are many
specimens of it in the British Museum from Port Elizabeth,
especially those bearmg my running no. 74, registered
Mitros 12-1 &e:
Group 4. ECHINOCLATHRINA.
9. Lchinoclathria tenuis.
Stipitate, compressed, very thin and leaf-like, lobed all on
one side of the stem, like a one-sided lobed leaf; lobes irregu-
larly denticulated on the margin. Consistence firm. Colour,
when fresh, ‘“ venetian red,” now brown. Surface minutely
and uniformly granulated. Spicules of three forms, viz.:—1,
skeletal, subpinlike, fusiform, curved, smooth, 45 by 14-
6000th, chiefly confined to the fibre; 2, subskeletal, also sub-
pinlike, very fine, thin, and long, 20 by 3-6000th, tending
356 Mr. H. J. Carter on
by its projection to give the surface a hispid or villous cha-
racter ; 3, echinating, also subpinlike, but smooth. Structure
rather open and reticulated on the surface, becoming more
compact towards the centre of the lamina. Size of specimen
7x7 in. and in. thick.
Depth 20 fath.
10. Hchinoclathria nodosa.
Stipitate, caulescent, branching, small specimen growing
on and over an Ascidian; branches nodulated, interuniting.
Consistence soft, resilient. Colour, when fresh, not mentioned,
now brown sponge-colour. Surface of branches uregularly
nodose, uniformly granulated over all. Vents in the sulci
between the nodulations. Spicules of two forms, viz. :—1,
skeletal, acuate, smooth, 35 by 1-6000th ; 2, echinating, also
acuate and smooth, 25 by 14-6000th ; the former confined to
the interior, the latter chiefly to the granulations on the sur-
face. Structure very compact throughout, but not axially
condensed or hardened. Size of specimen 3% in. high by
3 x 2 in. horizontally.
Depth 5 fath.
11. Echinoclathria subhispida.
Stipitate, compressed bunch of stalks with short stem ;
stalks cylindrical at first, then dividing at short distances
dichotomously and polychotomously, finally terminating in
flat, expanded, round ends more or less bifid. Consistence
firm. Colour, when fresh, ‘‘ venetian red,” now rich brown.
Surface uniformly granulated, subhispid. Pores and vents
not seen. Spicules of two forms, viz.:—1, skeletal, acuate,
smooth, 30 by 11-6000th, chiefly confined to the fibre; 2,
echinating, also acuate, smooth, small, thin, about 2(0-6000ths
long. Structure consisting of short-jointed tough fibre more
or less compact, becoming denser towards the axis. Size of
specimen 5 in. high by 5 x 4 horizontally.
Depth 11 fath.
12. Echinoclathria gracilis.
Stipitate, caulescent, branches long, very slender, irregu-
larly cylindrical, about } in. in diameter, dichotomously and
polychotomously divided near the stem, afterwards ending in
long stalks terminating in round ends. Consistence hard.
Colour, when fresh, “ dark red,” now dark brown. Surface
even, minutely granulated. Vents apparently few and scat-
tered. Spicules of two forms, viz. :—1, skeletal, acuate,
smooth, comparatively small, 25 by 1-6000th; 2, echinating,
small, acuate, fusiform, with slightly and terminally spined
ees
Sponges from South Australia. 357
head, 17 by 1-6000th. Structure hard, compact, firm through-
out, not condensed axially. Size of specimen 6 in. long.
Depth 20 fath.
Group 6. HIGGINSINA (new group).
13. Trachycladus levispirulifer, Carter (‘ Annals,’ 1879,
vol. ui. p. 848, pl. xxviii. fig. 1).
Obs. ‘There are two specimens of this sponge whose cylin-
drical branches dichotomously divided only once or twice are
12 in. long by 2 in. in diameter, diminishing towards the
points. They are chiefly remarkable for their bright colour,
said, when fresh, to be “ brilliant scarlet,’ now but little
faded. This colour is owing to the presence of an apparently
?symbiotic oscillatorian Alga, varying under 4-6000ths in.
long, and in its largest form consisting of four cells, of which
the terminal one at one end is conical or pointed. It is so
abundantly present and so much larger than the flesh-spicules,
which are again very small, that without close examination
the latter are apt to pass unnoticed.
Depth 19 fath.
Obs. It is a short oscillatorian Alga which gives the red and °
other bright colours to the Red Sea; also the cerulean cobalt
tint to the cerulean Suberitic sponge of this coast ; and some-
times living symbiotically with Spongelia pallescens, where
Dr. F. E. Schulze has actually found it to be present in plurality
in the ciliated embryo (Zeitschrift f. wiss. Zool. Bd. xxxil.
Taf. v. fig. 7), of which he kindly sent me a preparation.
14, Aigginsia coralloides, Higgin (‘ Annals,’ 1877, vol. xix.
plo xiv. fies I, Ge.)
Obs. Of this species there are two or three specimens, with a
variety, which may be described as follows :—
15. Higginsia coralloides, var. massalis.
Sessile, massive, lobate, contracted towards the base, con-
vex above. Consistence firm, resilient. Colour, when fresh,
““ dull purple,” now light mouse-colour. Surface uniformly
covered with meandering sulci separating correspondingly,
formed round linear elevations or ridges supporting a smooth
dermis. Vents small, very numerous, following the meander-
ing lines of the sulci between the ridges. Spiculation like
that of Higginsia coralloides, only here and there the acerate
is acuated.
Obs. All the specimens of Higginsia come from about the
same place or depth, viz. 11 fath., and all are stated to have
358 Mr. H. J. Carter on
been of a “ dull purple” colour when fresh. The occurrence
of the acwates in the variety ‘“ massalis”’ causes it to resemble
in spiculation H. natalensis, before described, of which the
type is in the British Museum.
18. Higginsia lunata (provisional).
Sessile, globular, massive, with a small mammilliform pro-
cess-growth over the surface. Consistence soft. Colour, when
fresh, ‘‘ dark slate,” which is the colour of the surface now,
but interiorly sponge-colour. Surface smooth, uniformly cover-
ing the small processes, which are conulated and accompanied
by an unusually thick, firm, reticulated dermis in the inter-
vals. Vents large, scattered over the surface. Spicules of
three forms, viz.:—1, skeletal, acerate, smooth, curved ; and
2, also skeletal, but acuate, smooth, curved, both about the
same size with gradationary forms between them; all about
120 by 2-6000ths; 3, flesh-spicule, acerate, much ‘curved,
often to a lunate form, microspined, often in groups parallel
to each other, simulating the development of a tricurvate,
about 9 by 4-6000th ; the former chiefly confined to the fibre,
the latter to the sarcode. Size of specimen 1 in. high by
3 x 3 horizontally.
Depth 19 fath.
Obs. The thick slate-coloured dermal layer is very character-
istic of this species, and its spiculation comes nearest to Hig-
ginsia, unless the microspined flesh-spicule should be nothing
but a spined tricurvate, when the resemblance would be so
much less that for the present I can only consider its “ seat”
as undetermined.
Fam. 2. Axinellida.
Group 7a. AXINELLINA.
17. Axinella chalinoides.
Stipitate, caulescent, dichotomous, cylindrical, branches of
different lengths, rather compressed, slightly diminishing in
size from the stem, which is short and thick, to the extremi-
ties, which are round. Consistence firm, resilient. Colour,
when fresh, ‘ dull brick-red,” now brown. Surface uniformly
but minutely granulated, and minutely hispid, often rendered
rather uneven by the presence of subjacent excretory canals.
Vents on the branches in two rows opposite to each other,
often accompanied by stelliform radiation, owing to the pre-
sence of subjacent but superficial excretory canals. Spicules
ef one form only, viz. a small, smooth, acuate, about 20 by
'
;
Sponges from South Australia. 359
1-6000th, in the fibre, and forming tufts (the granulations) on
the surface. Structure tough, dense, and compact. Size of
specimen 10 in. long, branches about 2 in. thick.
Depth 19 fath.
Obs. 'The subhispid character of the surface, the stelliform
venation around the vents formed by collapse of the dermal
sarcode over the subjacent excretory canals, and the compact
dense structure of the tissue generally, at once points out the
difference between this sponge and a caulescent-branched
Chalina.
18. Axinella chalinoides, var. glutinosa.
Stipitate, caulescent, cylindrical, branched, the latter
chiefly divided towards the terminations, which are compa-
ratively short and pointed. Consistence soft on the surface,
dense towards the axis. Colour, when fresh, “ chocolate,”
now brownish mouse-colour. Surface smooth, even, hispid
where the dark glutinous sarcode of the exterior has sunk
down upon the long acerate spicules during desiccation. Vents
chiefly in two lines opposite to each other on the cylindrical stalks.
Spicule of one form only, viz. acuate, but of different sizes,
the largest and longest 135 by 2.6000ths. Structure loose,
soft, and gelatinous on the surface from the thickness of the
dermis, becoming dense and hard towards the axis. Size of
specimen 8 in. long, larger branches about 4 in. in diameter.
Depth 20 fath.
19. Awinella setacea.
Stipitate, much compressed bunch of numerous branches,
radiating dichotomously and polychotomously from a short
stem ; branches cylindrical, terminating in sharp points, simple
and bifid at the ends respectively. Consistence soft, resilient.
Colour, when fresh, ‘dark yellowish brown,” now dark
brown. Surface granular, hispid. Ventsnotseen. Spicules
of one form only, viz. acuate, curved, smooth, of different
sizes, chiefly confined to the fibre, in and projecting through
it; the largest and longest which gives the setaceous character
210 by 42-6000ths ; another set but much smaller and shorter,
gathered together sheaf-like round the base of the long seta-
ceous one from the granulations on the surface. Structure
rather loose and soft externally, becoming compact towards
the axis. Size of specimen 44 in. high by 44 x 4 in. hori-
zontally.
Depth 7 fath.
20, Awinella atropurpurea.
Stipitate,. somewhat compressed bunch of dichotomously
360 Mr. H. J. Carter on
and polychotomously divided cylindrical branches, more or
less interunited clathrously, terminating elkhorn-like or poly-
chotomously, with obtuse rounded ends. Stem short and
thick. Consistence soft on the surface, hard in the axis.
Colour when fresh ‘ dark purple,” the same now, as this is
one of the few species which retain their colour, for it has
now been in spirit for upwards of a year and a half without
being the least altered in this respect, which may be owing
to the colouring-matter being contained in rather tough trans-
parent cells, where it exists in the form of several large black-
purple granules. Surface even, granulated, with granular
tufts of spicules. Vents small, here and there on the surface.
Spicules of one form only, viz. acuate, sub-pinlike, or slightly
inflated at the base, but of different sizes, the longest and
largest 300 by 73-6000ths, around which, towards the proxi-
mal end, a number of others of the same shape are gathered
sheaf-like, varying under 90 by 14-6000ths. Structure soft
on the surface, hard towards the axis. Size of largest speci-
men, for there are three of this beautiful sponge, 24 in. high,
including the stem, by 34 x 14 in. horizontally.
Depth 19 fath.
21. Axinella stelliderma.
Stipitate, compressed bunch of dichotomously and poly-
chotomously divided cylindrical branches, more or less amal-
gamating and interuniting on their way to the terminations,
which are conical and pointed singly or bifidly. Consistence
soft, resilient. Colour when fresh “purplish maroon,”
yellowish white now. Surface even, granulated, granules
smooth and round on the summit, stellately radiating towards
each other in reticulated lines of the fibrous dermis which are
thus arranged. Vents not seen. Spicules of one form only,
viz. acuate of different sizes, the longest and largest about
180 by 2-6000ths, projecting from the summit of the granule
and surrounded at its base sheaf-like by a number of shorter
ones. Differing from the following variety, viz. Aadnella
stelliderma, var. acerata, only in the form of the spicule, which
is acuate instead of acerate. Structure soft on the surface,
hard and compact towards the axis. Size of the largest
specimen, for there are two, 7 in. high by 7 x $ horizontally.
Depth 10 fath.
22. Axinella stelliderma, var. acerata.
Stipitate, compressed bunch of short, thick, cylindrical,
dichotomously and polychotomously divided branches, more
Sponges from South Australia. 361
or less interuniting and amalgamated; simple or bifid at the
ends, which are conical. Consistence soft, resilient. Colour
when fresh ‘dull purple,” now yellowish white, opaque.
Surface even, largely granulated; granules smooth, radiating
star-like, the rays being part of the dermis, interuniting with
each other reticulately between the granules. Vents not seen.
Spicule of one form only, viz. acerate, fusiform, smooth, finely
pointed, 75 by 1-6000th. Structure soft on the surface,
becoming compact and hard towards the axis. Size of speci-
men 33 in. high by 4x 13 in. horizontally.
Depth 20 fath.
23. Awinella villosa (dry specimen).
Stipitate bunch of caulescent dichotomous branches, rising
from a short, thick, round stem, spread out at the base for
attachment; branches cylindrical, dividing near the stem,
diminishing in size towards the extremities, which are bifid
and pointed. Consistence soft on the surface, hard in the
axis. Colour when fresh not stated, now brown-grey. Sur-
face now, in its dried state, roughly reticulated and shagey,
from the subsidence of the sarcode between the subjacent
spiculiferous tissue, which thus appears clotted together like
that of Dictyocylindrus rugosa, Bk. Spicules of one form
only, viz. acerate, curved, smooth, about 78 by 24-6000ths.
Structure loose on the surface, becoming condensed and hard
towards the axis. Specimen 7 in. high by 3x98 in. horizon-
tally ; branches about $ in. in diameter.
Depth not stated.
The above species being branched and caulescent are very
much like those of the group Dictyocylindrina, differing only,
as before stated, in the absence of the echinating spicule.
24. Axinella flabellata.
Stipitate, compressed expanded, thickish, lobate ; margin
irregular; stem short, angular and thick. Consistence firm,
resilient. Colour when fresh ‘“ brown-grey,” now dark
sponge-colour. Surface even, minutely granulated. Vents
not seen. Spicules of three forms, viz. :—1, skeletal, acuate,
70 by 2-6000ths, chiefly confined to and projecting through
the fibre ; 2, “‘ trichites,” loose and in sheaf-like bundles, about
12-6000ths long ; 3, flesh-spicule, bihamate, C- and S-shaped,
simple and contort, 4-6000ths long, both the latter abundant
and confined to the sarcode. Structure compact, becoming
more condensed and hard towards theaxis. Size of specimen
3} in. high by 44x 1} in. horizontally.
Depth 18 fath.
362 Mr. H. J. Carter on
Obs. This specimen has a piece of Darwinella australiensis
about an inch in diameter growing upon its flat surface.
25. Axinella pilifera.
Massive, lobed, contracted towards the base, lobes more or
less compressed. Consistence soft. Colour when fresh
“ orange-brown,” now light brown. Surface covered with
conuli, from the summit of each of which projects a
coarse single filament of the fibre charged with the spicules of
the species, giving the whole a hairy appearance. Vents
small, scattered here and there over the lobes. Spicules of
one form only, viz. acerate, 65 by 2-6000ths, chiefly confined
to and projecting through the fibre. Structure rather loose
generally. Specimen 3 in. high by 34x 1} in. horizontally.
Depth 20 fath.
26. Axinella meloniformis.
Massive, globular, sessile, ridged meridionally like a melon,
with a depression on the summit. Consistence firm. Colour
when fresh “‘ orange,” now pale yellow. Surface uniformly
granulated, covered by a smooth dermis. Spicule of one
form only, viz. acerate, 150 by 4-6000ths. Structure com-
pact, hard, rough. Presenting immediately under the dermis
a layer of large ? epithelial, nucleated, and granuliferous cells,
chiefly elliptical in form, and about 10-6000ths in the longest
diameter, accompanied by a layer of much smaller ones zn the
dermis, ? the real epithelial cells. Size of specimen 1 x 1 x iin.
Depth 11 fath.
Obs. The presence of these large circular and elliptical
nucleated and granuliferous cells, such as are found in several
sponges (ex. gr. Dereitus niger, &c., ‘ Annals,’ 1871, vol. vil.
pl. iv. fig. 6, &c.), also in the Australian “new species” of
Luffarida (? Dendrilla rosea, Lendenfeld) to which I have
alluded as probably a new species in the ‘ Annals’ of 1885,
vol. xv. p. 202, &c., is interesting because they are underneath
the fibrous dermis which is covered on the immediate surface
with much smaller, ? the real epithelial cells, while the larger
ones can hardly be considered to be ova, as they are confined
to the position mentioned. ‘They are pigment-cells in Der-
citus niger.
27. Axinella solida.
Sessile, spreading, thick, cork-like mass. Consistence soft.
Colour when fresh “orange,” now sponge-colour. Surface
undulating, cauliflower-like, consisting of short pointed granu-
Sponges from South Australia. 363
lations. Pores and vents not seen. Spicules of one form
only, viz. acuate, about 100 by 3-G000ths, situated in the
interior of and projecting. through the fibre. Structure
columnar, composed of erect plumosely-tufted filaments in
juxtaposition, ending in the granulations of the surface. Size
of specimen } in. high by 2 x 2 in. horizontally.
Depth 11 fath.
Group 7 6. PHAKELLINA.
28. Phakellia flabellata.
Substipitate, contracted towards the base, expanding into a
flabellate form with irregularly undulating round border.
Consistence resilient. Colour when fresh “ yellow-buff,” much
the same now. Surface undulating, uniformly granulated.
Pores and vents not conspicuous. Spicules of two forms,
viz. one acuate, the other acerate, both about the same size,
viz. 40 by 14-6000ths, chiefly confined to the fibre, which,
ending on the surface in spiculiferous tufts, produces the
granulated character. Structure compact, hardening towards
the central plane, from which the fibre curves upwards and
outwards to the surface on each side. Size of specimen 2 in
high by 4 x $ in. horizontally.
Depth 20 fath.
29. Phakellia crassa.
Stipitate, flabellate, winged proliferously, thickish ; margin
round, irregularly undulating. Consistence firm, resilient.
Colour when fresh ‘‘ wax-yellow,” now yellowish brown.
Surface uniformly covered with papillary elevations about
4-12ths inch apart, supporting a granulated dermis. Vents
small, stelliform, on the summits of the papillary elevations.
Spicules of one form only, viz. acuate, small, stout, about
60 by 24-6000ths. Structure plumose, fibre curving up-
wards and outwards from the central plane, where it is
condensed, to the surface on each side, where it is loose, and
ends in tufts of spicules which form the granules. Size of
specimen 6 in. high by 5 in. horizontally ; lamina 5-12ths in.
thick.
Depth 20 fath.
30. Phakellia brassicata.
Stipitate, vase-lke rosette head, dividing at once from a
longish stem into several short, somewhat compressed flabellate
branches, which expand into still more compressed, thin, leaf-
like divisions, about 1-8th in. thick; alate, proliferous, and
364 Mr. H. J. Carter on
wavy, interunited with each other, tending to a foliate arrange-
ment, but well separated, terminating in denticulated margins.
Consistence hard. Colour when fresh “ orange-red,” now
brown. Surface smooth, with a finely reticulated dermis,
supported on short hispid fibre. Spicules of one form only,
viz. acerate, 60 by 14-6000ths. Structure loose on the sur-
face, hardening towards the axis. Size of specimen 54 in.
high, including the stem, which is 24 in. long, 44x 3 hori-
zontally across the brim.
Depth 19 fath.
Group 7c. ACANTHELLINA.
31. Acanthella cactiformis, Cart. (‘ Annals,’ 1885,
vol. xv. p. 114, pl. iv. fig. 6).
Obs. Of this there are two specimens, viz. one dry, that to
which I have alluded, and the other wet, which is much
smaller and of which the depth was 19 fath.
32. Acanthella hirciniopsis.
Flabellate, with denticulated border and thorn-like iregu-
larly conulated surfaces. Consistence soft outside, covering
an extremely dense and compact massive skeletal frame.
Colour when fresh ‘ venetian ‘red,’ now mouse-colour. Sur-
face most irregular in growth, especially on one side, covered
with prominent conuli, most regularly distanced; each
conulus smooth over the point where it is covered with a
beautifully reticulated dermis, which, descending to the inter-
conular spaces in a radiating form, becomes continuous with
that of its neighbours, very much like that of a Hircinia.
Epithelial cells, if any, very small, inconspicuous. Pores in
the interstices of the dermal reticulation. Vents here and
there, chiefly on the border. Spicules of one form only, viz.
long, acerate, of various sizes under 110 by 14-6000ths.
Structure of the dermal reticulation soft, composed of fusiform
fibrille, without foreign substances; epithelial cells small and
inconspicuous. Structure of the interior soft towards the
surface, becoming densely compact towards the centre, which,
when a portion is macerated, comes forth as a fenestrated
skeleton composed of an intensely tough hard condensation
of horny sarcode and the spicules of the species amassed
together. Size of specimen, which is only part of the ori-
ginal, from which it has been cut off, 6 in. high by 41x 1 in.
horizontally.
Depth 19 fath.
Sponges from South Australia. 365
Obs. There are two specimens of this sponge, both of which
appear to have been cut off from much larger specimens, too
large probably in their entirety to be put into the opening of
the tin case in which they were sent, so that my description
has been taken from that which appears to afford the most
characteristic features; the other is much larger and more
ragged, that is irregularly grown over on the surface, which
thus in some places gives it a thickness of 3 inches. Its
colour when fresh is stated to be ‘“ buff-brown, with tints of
red.” The conuli where uniformly distributed are 2-12ths in.
apart, but where irregularly scattered sometimes 5-12ths in.
apart, with great prominence and depth between them, which,
being filled up by the dermal reticulated fibrous structure,
at first sight, as before stated, gives them very much the aspect
of asponge belonging to the conulated Hircinida or Aplysinida,
excepting that there are no foreign substances in the fibre
and very small epithelial cells in the dermis. Depth of both
specimens 19 fath.
33. Acanthellina parviconulata.
Sessile, erect, tall, lobate, fenestrated, more or less regu-
larly covered with short thorn-like conuli. Consistence soft
on the surface, dense in the interior. Colour when fresh
“* ovey, tinged with terra-cotta red,” now grey only. Surface
extremely irregular and jagged from the presence of prolife-
rous growths, covered with short thorn-like conuli supporting
a fibro-reticulated dermis which conceals their points, thus
rendering them round, and fills up the depressed intervals
between them, very much like that of a Hircinia, only the
conuli are much smaller and more numerous than in the fore-
going specimen; hence the designation ‘ parviconulata.”’
Vents numerous and large, especially over one of the erect
lobes. Spicules of two forms, but very much alike in size,
viz. one acuate and the other acerate, the latter abruptly
pointed, each averaging about 60 by 2 to 3-G000ths. Struc-
ture soft on the surface, where the dermis, although of finer
texture, is otherwise the same as that described under Acan-
thella hircinopsis, covering the same kind of densely-packed
spiculiferous white skeletal framework. Size of specimen
6 in. high by 2 x 1} in. horizontally.
Depth 18 fath.
34. Acantheilina rugolineata.
Somewhat compressed, massive, sessile, contracted towards
the base, furrowed and correspondingly ridged with rough
linear elevations. Consistence extremely soft. Colour when
Ann, & Mag. N. Hist. Ser. 5. Vol. xvi. 5
366 Mr. H. J. Carter on
fresh not stated, now light whitish yellow. Surface cacti-
form, covered by a reticulated dermis. Pores in the inter-
stices of the dermal fibro-reticulation. Vents here and there
along the upper part. Spicules of two forms, viz. acuate and
acerate, both about the same size, viz. 80 by 24-6000ths, and
both merging into each other by gradational variation, chiefly
confined to the interior of the fibre and projecting through it.
Structure soft on the surface, condensed to hardness internally,
thus forming a solid skeletal mass of spicules and sareode
like that of the foregoing species. When dry the dermal
structure, by its dark brown translucent gluey appearance and
nature, contrasts strongly with the opaque white skeletal fabric
beneath, as in A. cactiformis. Size of specimen about 2 x 2
x 2 in.
Depth not stated.
Group 7 f. LEUCOPHL@INA.
35. Ciocalypta penicillus, Bk. (Mon. B.S. vol. iii.
pl. xi. fig. 2, &c.), var. aciculata.
Obs. The only difference between this and Dr. Bowerbank’s
specimen is that the spicule is sub-pinlike, with fusiform
shaft, instead of simply acuate. Depth 9 fath.
36. Crocalypta Tylert, Bk. (Proc. Zool. Soc. 1873,
Pleciveqtioes)):
Obs. Of this there are two specimens, depth 19 and 11
fath. respectively.
37. Leucophlea massalis, Cart. (‘ Annals,’ 1883,
vol. xii. p. 323, pl. xiv. fig. 15).
Depth 19 fath.
Fam. 3. Pseudoechinonemida.
ECGHINONEMATINA ARENACEA,
38. Wilsonella australiensis.
Flabelliform, stipitate, wavy, undulating in lines radiating
from the base to the circumference ; stem short. Consistence
firm, resilient. Colour when fresh “ white,” much the same
now. Surface areniferous, scattered over uniformly with
papillary elevations about 5-12ths in. apart, on the summit of
each of which is a large vent defined by a circular thin mar-
Sponges from South Australia. 367
gin. Spiculation that of Hchinonema anchoratum (‘ Annals,’
1881, vol. vi. p. 379), viz.:—1, smooth acuate, 25 by
$-6000ths, chiefly confined to the centre of the fibre, with
grains of sand and foreign objects; 2, echinating spicule, a
spiniferous acuate, 16 by 1-6000th ; 3, flesh-spicule a navicu-
liform equianchorate confined to the sarcode, 34-6000ths.
Structure compact throughout, without axial or central con-
densation. Size of specimen, which is wet, 7 in. high by
7x in. horizontally.
Depth 6 fath.
Obs. There is also a dry specimen of this species 10 in.
high by 9x 5 in. horizontally, composed of a large group of
flabelliform plicated lobes of different sizes below the single
one above mentioned, more or less proliferous and twisted in
form, some of which are anything but like the typical one
above described, yet all evidently modifications of the same
plan, rising and spreading into a great group florally from a
contracted subsessile base, about 24 in. in diameter.
It is this specimen which I have briefly described in the
‘Annals’ of 1885 (vol. xv. p. 320) under the above name,
and of which there are several others of a like kind in the
British Muséum, all of which come from the south coast of
Australia, and bear my running no. “128.” As sponges on
being dried generally shrink up to half their natural size, the
dried one just mentioned must originally have been twice
that above stated, so that when fresh it must have been a still
more magnificent specimen than it is at present. The genus
has been named after Mr. J. Bracebridge Wilson, M.A.,
F.L.S., of the Church of England Grammar School, Geelong,
Victoria colony, South Australia, to whom, as before stated, [
am indebted for all these sponges, both wet and dried.
PLUMOHALICHONDRINA ARENACEA.
39. Plumohalichondria arenacea,
Irregularly club-shaped, sessile, massive, lobed, tall, high,
enclosing shells and sand at the base, which is contracted.
Consistence tough, firm, resilient. Colour when fresh not
mentioned, now pale yellow throughout. Surface uniformly
granulated, covered by a minutely reticulated dermis. Vents
rather small, scattered over the surface generally. Spicules
of three forms, viz. :—1, skeletal acerate (the tibiella) nearly
straight, 40 by 14-6000ths, chiefly confined to the centre of
the fibre, with grains of sand and foreign objects; 2, spined
acuates more or less bent, of different sizes under 32-6V00ths
25*
368 Mr. C. Chilton on Polymorphism
long, chiefly echinating the fibre in great abundance; 3,
angulated equianchorate, about 3-6000ths long, confined to the
sarcode. Structure throughout uniformly compact, tough, and
firm, without axial condensation. Size of specimen 1J in.
high by 24 in. in diameter in its widest part.
Depth 6 fath.
Obs. This is evidently a Plumohalichondria which, in
addition to its self-made or proper spicules, has taken in
foreign substances for the axial support of its fibre.
P.S.—The general forms of the specimens respectively
above given can only be taken cet. paribus as characteristic
ot the species, since the growth of sponges is so frequently
more or less influenced in their form by the environment,
that unless a great number of specimens of the same species
have been seen it is impossible to determine this accurately.
[To be continued. ]
XXXII.—On an Example of Polymorphism in the Amphi-
poda. By Cuartes Cytron, M.A. (New Zealand).
[Plate X.]
SEVERAL instances of dimorphism in the Crustacea are already
known. Fritz Miller, who seems to have been the first to
call attention to examples of it in this group, has given two,
one in the Isopoda (Tanais)* and one in the Amphipoda
(Orchestia) +; in each of these cases there are two forms of
the male to one of the female. Mr. G. M. Thomson has re-
corded a similar example from the terrestrial Orchestia of
New Zealandt. From the examination of a large number
of specimens of Orchestia gathered from several different
localities in New Zealand he comes to the conclusion that
they all belong to one variable species, Orchestia sylvicola,
the “ males of which have at least two forms of the gnatho-
oda.” Another example is found in Mera subcarinata,
Haswell (7. Petrie?, G. M. Thomson); but here the two
forms of the males only differ very slightly from one another.
In specimens taken by Mr. Thomson at Stewart Island, New
Zealand, the males had ‘‘the whole lower surface [of the
propodos of the posterior gnathopoda] very densely fringed
* ‘Facts for Darwin, i 20. t Z.e. p. 24.
{ ‘Transactions New-Zealand Institute,’ vol. xiii. p. 212.
in the Amphipoda. 369
with two rows of long simple hairs,” and specimens taken by
myself in Sydney agree exactly with this description, while
those from Lyttelton Harbour differ in that these long simple
hairs are entirely absent, and in having the palm more di-
stinctly defined and more uneven, and the dactylos more
rounded at the end *.
As Fritz Miiller says, “the occurrence of two kinds of
males in the same species may perhaps not be a very rare
phenomenon in animals in which the males differ widely from
the females in structure. But only in those which can be pro-
cured in sufficient abundance will it be possible to arrive at the
conviction that we have not before us either two different
species or animals of different ages”. In view of this danger
I would like to point out that I have not as yet had a sufli-
cient number of specimens of Mera subcarinata to make me
feel quite sure that the two forms are not simply animals of
different ages. Iam the more doubtful in this case because
Mr. Walter Faxon has recently shown that what were con-
sidered to be dimorphic forms of the male in certain species
of Cambarus are really “ alternating periods in the life of the
individual, the ‘ first form’ being assumed during the pair-
ing-season, the ‘second form’ during the intervals between
the pairing-seasons ’’t.
In many genera of the Amphipoda, such as Mera, Melita,
Paranenia, Podocerus, &c., the females of different species are
often much more alike than the corresponding males, which
usually have some of their limbs abnormally developed ; hence
if a supposed case of dimorphism or polymorphism occurs in
these genera it is more than usually difficult to decide whether
we have several species of which the females are alike, or nearly
SO, or one species with several forms of the male to one of the
female. I have, however, an instance to bring forward from
the genus Microdeuteropus, and, though I have hesitated for a
long time, I think I have now sufficient evidence to show that
we have here a widely dispersed species which has three forms
of the male and only one of the female.
In 1879 Mr. G. M. Thomson described a species of Micro-
deuteropus from Dunedin Harbour, giving it the name of JZ.
maculatus; at the same time he recorded the existence of
Aora typica in New Zealand, the species having been origi-
nally obtained at Valparaiso§. In a subsequent paper he
* «Transactions New-Zealand Institute, xv. p. 82; ‘New-Zealand
Journal of Science,’ ii. p. 230; and ‘Proceedings Linnean Society
N.S. W.’ vol. ix. part 4, p. 1039,
+ ‘Facts for Darwin,’ p. 24.
‘American Journal of Science,’ vol. xxvii. p. 42.
§ Ann. & Mag. Nat. Hist. ser. 5, vol. iv. p. 381.
370 Mr. C. Chilton on Polymorphism
remarked upon the resemblance of Microdeuteropus maculatus
to Aora typica in the following words :—‘ Though dissimilar
In many respects from Aora typica, there is such a strong
resemblance in other points that I should. not be surprised if
they prove to be male and female of the same species, in
which case the generic character of Aora will require modifi-
cation. Can it be a case of protective resemblance ?” *.
In 1881 I took numerous specimens of Mcrodeuteropus
maculatus in Lyttelton Harbour, and with them a form closely
resembling them in all respects except in the first gnatho-
poda, which were ‘‘complexly chelate,” like those of Aora
typica, though differmg in some minute details; and in a
paper published in the ‘Transactions of the New-Zealand
Institute,’ vol. xiv. p. 173, I suggested that most probably
this form rather than Aora typica was the male of Microdeu-
teropus maculatus. (In referrmg to this form I shall speak of
itas ‘ Microdeuteropus maculatus g,Chilton.”) Afterwards
I took Aora typica also im Lyttelton Harbour, and was thus
able to see that, though it was really somewhat different from
Microdeuteropus maculatus g, Chilton, as I had previously
stated, it was, like that form, essentially similar to Mcro-
deuteropus maculatus 2 , ‘Thomson, except in the first gnatho-
poda. About the same time I heard by letter from Mr.
Thomson that he had taken a large number of specimens of
Aora typica and Microdeuteropus maculatus 2, both at the
same locality, and felt convinced that they both belonged to
one species. While in Sydney, in January 1884, I obtained
specimens of Microdeuteropus Mortoni, Haswell, and also of
M. tenuipes, Haswell. One of my specimens of the latter
species was a female bearing eggs, and from the close resem-
blance of the two I suggested f that IZ. Mortont was probably
the male of M/. tenuipes. J also remarked upon the very close
resemblance between J/. tenuipes and M. maculatus ? , and
between JM. Mortoni, WM. maculatus g, Chilton, and Aora
typica, in all points except in the first gnathopoda; but at
the time I left the species as distinct, until further evidence
should be forthcoming. Since then I have examined the
various forms more minutely, and have compared them with
Dunedin and Stewart-Island specimens of J. maculatus 9
and Aora typica, which were very kindly placed at my dis-
posal by Mr. Thomson, and I now feel convinced that they all
belong to one species, of which we therefore now know three
forms of the male and one of the female.
The different forms vary somewhat in several small points ;
* «Transactions New-Zealand Institute,’ xiii. p. 218.
t ‘Proceedings Linnean Society N.S. W.’ vol. ix. part 4, p. 1040,
in the Amphipoda. | BYE
thus the relative lengths of the various joints of the antenne
are subject to slight variations ; in large specimens the lower
antennee increase in length as compared with the upper, and
the flagellum of the upper antenna decreases in length as
compared with the peduncle.
The stout curved sete on the end of the flagellum of the
lower antenna in Microdeuteropus tenuipes, mentioned by Mr.
Haswell, are present in the other forms; but in many of the
specimens they are not very prominent, and they have conse-
quently not been mentioned by other observers.
Mr. Thomson described the appendage to the mandible of
Microdeuteropus maculatus as two-jointed. In MM. Mortoni,
M. tenuipes, in the Lyttelton specimens of JM. maculatus, both
male and female, and of Aora typica, it is three-jointed, as is
almost universally the case with the Amphipoda, and in the
Dunedin specimens of WM. maculatus and Aora typica which
I dissected I found it also three-jointed ; the first and second
joints lie nearly in the same straight line, and though the
division between them is distinct enough, they do not appear
to be very movable one upon the other; and I fancy this has
given rise to the error in Mr. Thomson’s description, which is
im all other respects exceedingly accurate. In this species, as
in many others of the Amphipoda, the cutting-edge of the
mandible is not quite the same on the right side as on the
left, but the differences in this case are small. On the distal
portion of the third joint of the appendage are two rows
of long serrated hairs, of which those at the end are the
longest and are most closely approximated to one another,
and between these are two rows of short straight sete. It is
not very easy to get a good view of these rows in the proper
position ; when seen in side view they present the appearance
of a dense fringe on one side of the joint, as shown in Mr.
Thomson’s figure*. In his description of Aora typica
Mr. Thomson says, “telson quite smooth.” In all the speci-
mens that I have examined the telson is essentially the same as
in Microdeuteropus maculatus, viz. the projecting portion on
each side is slightly notched at the end and bears one or two
slender spinules.
It is curious to note the variations in the parts in which the
males and females of different species of the Amphipoda re-
semble and differ from one another. ‘Thus in some species
of Mera, such as M. subcarinata, M. festiva, and in Melita
tenuicornis, Podocerus frequens, Podocerus longimanus, Para-
nenia typica, Nicea egregia, &c., the male differs from the
female in the structure of the second pair of gnathopoda, while
* Ann, & Mag. Nat, Hist. ser. 5, vol. iv. pl. xvi. fig. 7,
372 Mr. C. Chilton on Polymorphism
in all these species the jist pair are the same in the male as in
the female. In the forms under consideration exactly the
reverse is the case: the male forms differ from the female in
the structure of the jist pair of gnathopoda, while in Aora
typica, Microdeuteropus Mortoni, M. tenuipes, M. maculatus § ,
and M. maculatus 2, the second pair of gnathopoda is essen-
tially the same throughout; and the following description
drawn up from Lyttelton specimens of M. maculatus 9 will
apply, with the slight variations afterwards mentioned, to
the second gnathopoda of all the other forms.
The meros (see Pl. X. fig. 5) is rather pointed distally and
has the distal margin supplied with a row of long sete; the
carpus is triangular, the inferior or posterior edge rounded and
abundantly supplied with sete arranged in short transverse
rows, the sete being longest towards the distal end; there
is also on the side of the carpus, near its distal end, an oblique
row of about six long sete, and more proximally a much
shorter row of from two to three sete ; on the upper or anterior
margin are two or three small tufts, the last being situated at
the antero-distal angle ; the propodos is of the same width as
the carpus and has the palm slightly convex, transverse, or
but slightly oblique, very minutely serrated, and with a some-
what irregular fringe of rather short sete, and defined by a
stout seta; the posterior edge of the propodos is thickly sup-
plied with sete arranged in about six short transverse rows or
tufts; on the anterior edge are five similar rows, each con-
taining about five sete, the last one being at the base of the
dactylos, and on the side of the dactylos are four or five
similar short transverse rows of sete, arranged in one longi-
tudinal line; the dactylos is fairly stout, inner edge finely
serrated, the serrations increasing in size until near the extre-
mity, which is, however, smooth. All the sete: on the poste-
rior margin of the meros, carpus, and propodos appear to be
serrated throughout the distal half of their length, and many
are slightly bent in the centre, while those on the palm and
on the anterior margin of the various joints are simple.
In the specimens of JMcrodeuteropus maculatus 2 which
Mr. Thomson sent me the second gnathopoda agreed very
closely with the description given above, but had the palm
rather more transverse than in my Lyttelton specimens. Aora
typica, both Lyttelton and Dunedin specimens of which were
examined, also agrees with this description, but has the palm
more oblique, and generally has a greater number of sete
than in Muicrodeuteropus maculatus 9, though they are
arranged in precisely the same manner.
The first gnathopod (see Pl. X. fig. 6) of Microdeuteropus
in the Amphipoda. 373
maculatus ¢ is somewhat larger than the second, but is of the
same general shape; the carpus bears numerous sete irregu-
larly arranged on the posterior margin; on the anterior
margin there is only one tuft at the antero-distal angle; the
propodos is supplied with many sete arranged as in the second
enathopod; the palm is very oblique, slightly curved, and is
defined by a stout spine or seta, which is much more promi-
nent than the corresponding one in the second gnathopod.
The length of the palm varies considerably ; in a tracing of
a drawing made by Mr. ‘Thomson, which he has sent me, the
palm is represented as occupying almost the whole of the
posterior margin of the propodos; in the figure which I give
(Pl. X. fig. 6), taken from a female bearing eggs, it is
scarcely more than half as long as the propodos; it most
probably increases in length with the age of the animal. The
dactylos is stout and strongly curved, and is similar to that of
the second gnathopod.
In Aora typica (see Pl. X. fig. 2) the coxa of the first
gnathopod is produced anteriorly imto a sharp point, as in
Aora gracilis* ; the basos is long and is produced into a
tooth on the anterior margin at a point not far from the base
of the joint; there are a few very small sete at intervals
along the anterior margin; at the distal end the integument
is produced anteriorly and distally, so as to form a thin plate,
which interlaps with a similar but larger plate arising from the
ischios. ‘lhe meros is produced inferiorly into a long acute
spine, which is as long or very nearly as long as the carpus;
the carpus is longer than the propodos, sides parallel, posterior
with a few small tufts of sete near the distal end; propodos
slightly arcuate, with no distinguishable palm in full-grown
specimens ; the distal portion thickly covered with long hairs,
arranged in short transverse rows and most numerous at the
base of the dactylos. Dactylos slightly curved, of nearly
the same width throughout until it narrows suddenly near the
end.
In smaller and presumably younger specimens there is a
stout seta about the centre of the inferior margin of the pro-
podos, marking off what may be considered a ‘“ palm ;”’ this
is entirely absent in large specimens (see Pl. X. fig. 3). In
these young males the first gnathopod is much more like
the first gnathopod of the female than in the full-grown males.
I have already described a case similar to this in Podocerus
longimanus }.
* See Bate and Westwood, ‘ British Sessile-eyed Crustacea,’ figure on
p- 281, vol. 1.
1h Transactions New-Zealand Institute,’ xvi. p. 256.
374 Mr. C. Chilton on Polymorphism
The plates into which the integument is produced on the
outer sides of the basos and ischios interlap, and appear thus
to strengthen the joints, which would otherwise be weak for
so long a limb, and they also serve to keep the carpus firmly
in its place when that joint is laid back upon the basos, as it
usually is when the limb is not being used. The tooth on
the anterior margin of the basos seems to be of use for the
same purpose. Spence Bate speaks of it as ‘an apparently
useless tooth ” *.
In Microdeuteropus maculatus g, Chilton (see Pl. X. fig. 1),
the first gnathopod has the basos long, expanding slightly
distally ; ischios nearly twice as long as broad, both joints
being almost free from sete; the meros is narrow and is
produced inferiorly into a long acute spine reaching beyond
the end of the carpus; it is slightly curved towards the extre-
mity and bears on its inferior or posterior margin a small tuft
of sete at about one third of the length of the joint from its
extremity ; the carpus is very large, more than twice as long
as broad, and bears a very few short setee at the distal end;
the propodos is rather more than half the length of the carpus,
and is much narrower, and becomes narrower towards the
distal end ; inferior margin very slightly concave and thickly
fringed with sete more or less regularly arranged in tufts ;
there is also a tuft on the anterior margin at the base of the
dactylos; dactylos more than half as long as the propodos,
narrowing regularly towards the extremity, where there are
a few short setee on the inner margin.
In general shape the first gnathopod of IMicrodeuteropus
Mortoni, Haswell (see Pl. X. fig. 4), closely resembles that
of M. maculatus g, Chilton, but the sete are very different,
and there are also a few other small differences: the anterior
edge of the basos bears a thick fringe of rather long sete ;
these sete are sparsely plumose towards the distal ends;
similar setee are found on the anterior edge of the ischios and
on both lateral borders of the meros, which is hollowed out
anteriorly to receive the carpus; the sete on the meros are
more or less regularly arranged in tufts, but the acute-pointed
end of the joint is naked; ordinary simple setee are found on
the anterior margin of the carpus and on both margins of the
propodos ; the dactylos is very long, fully as long as the pro-
podos, and bears three or four tufts of sete on its concave
margin.
It is evident from what I have already said that the genera
* ‘ British Sessile-eyed Crustacea,’ i., Introduction, p. li.
in the Amphipoda. 375
Aora and Microdeuteropus will have to be combined * ; and
as Aora is the older genus, that name will have to be retained.
~The specific name typica has priority over all the others, so
that the name of our species will be Aora typica.
I give the synonymy so far as known to me and brief dia-
gnoses of the various forms.
Aora typica.
Aora typica, Kroyer, Tidsskr. ser. 2, p. 828, pl. iii. fig. 3; Spence Bate,
Cat. Brit. Mus. Amphip. p. 161, pl. xxix. fig. 3; G. M. Thomson,
Aun. & Mag. Nat. Hist. ser. 5, vol. iv. p. 831; Trans, New-Zealand
Inst. vol. xiii. p. 216.
Lalaria longitarsis, Nicolet, Gay’s Hist. de Chile, iii. pl. ii. fig. 8.
Microdeuteropus Mortoni, Haswell, Proc. Linn. Soc. N. 8S. W. vol. v.
. 889, pl. xxii. fig. 2; Cat. Australian Crust. p. 264; Chilton, Proc.
inn. Soc. N. 8. W. vol. ix. p. 1040.
Microdeuteropus tenuipes, Haswell, U. c. vol. v. p. 389, pl. xxii. fig. 1;
Chilton, 7. ¢. vol. ix. p. 1040.
Microdeuteropus maculatus, G. M. Thomson, Ann. & Mag. Nat. Hist.
ser. 5, vol. iv. p. 831, figs. 5-8; Trans, N.-Z. Inst. vol. xiii. p. 217,
figs. 7A, B, and C; Chilton, Trans. N.-Z. Inst. vol. xiv. p. 173,
fig. 3, a-0.
Female. Animal smooth, slender. Superior antenne: con-
siderably longer than inferior ; second joint of peduncle long
and slender; third short, and furnished with a 5-6-jointed
secondary appendage; flagellum very slender, many-jointed,
sparingly ciliated. Inferior antenne strong, subpediform ;
third jot of peduncle short, fourth and fifth very long; fla-
gellum shorter than last joint of peduncle, with stout curved
sete in addition to the ordinary slender hairs. Gnathopoda
of moderate size, both strongly ciliated; first pair the largest ;
propodos about as large as the carpus; palm very oblique,
almost longitudinal, slightly curved, and defined by a strong
spine; dactylos serrated on inner margin ; second pair similar,
but with palm transverse or but slightly oblique. Fourth and
fifth pairs of pleopoda with stout straight spines; sixth pair
with two or three spines like those of the preceding pairs, and
with a few longer and more slender spines or hairs. ‘Telson
raised on each side into an upward projection, each having the
apex notched and bearing two or three slender spinules. —
Male. Vhree forms, all differing from the female in the
character of the first gnathopod, which in each has the meros
produced into a long spine reaching about to the end of the
carpus.
* The necessity for this was indeed recognized by the Rey. T. R. R.
Stebbing as far back as 1878. See Ann. & Mag. Nat. Hist. ser. 5, vol. ii.
p- 369.
376 Mr. R. Rosenstock on Australian Lepidoptera.
The forms may be distinguished as follows :—
1. (Aora typica, Kroyer.) —Basos with a tooth projecting
forwards on the anterior margin; carpus longer than the
propodos, but of about the same breadth.
2. (Microdeuteropus maculatus g , Chilton.) —Carpus longer
and broader than propodos; meros with small tuft of sete
on posterior margin. _
3. (Microdeuteropus Mortoni, Haswell.)—Carpus longer
and broader than the propodos; meros hollowed anteriorly
and with each lateral margin densely fringed with setz ;
dactylos as long as propodos and with two or three tufts of
setes on concave border.
EXPLANATION OF PLATE X.
Aora typica.
[ All the figures much erlarged. |
Fig. 1. First enathopod of male, second form (Microdeuteropus maculatus
3, Chilton).
Fig. 2. First enathopod of male, first form (Aora typica), seen from outer
side.
Fig. 8. First gnathopod of an immature specimen of the same form, seen
from the inner side.
Fig. 4. First gnathopod of male, third form (Microdeuteropus Mortont).
Fig. 5. Second gnathopod of female (7. maculatus).
Fig. 6. First gnathopod of female (MZ. maculatus).
XXXIV.—Notes on Australian Lepidoptera, with Descrip-
tions of new Species. By RupotpH Rosenstock, B.A.
[Plate XI.]
Tue following is an account of a small collection of Lepido-
ptera from South Australia forwarded to the British Museum
by Dr. Lucas, of Melbourne.
A number of the specimens were unfortunately in poor
condition, being either broken or so much worn as to render
identification difficult; and description, in the case of some
possibly new species, undesirable. I am nevertheless enabled
to describe twenty-eight species, in better condition than those
just mentioned, as new to science.
The Microlepidoptera were well represented, as one might
expect in collections from this region.
Mr. Meyrick’s labours in this division of Lepidoptera
aftorded me much aid, though I discovered one or two
Mr. R. Rosenstock on Australian Lepidoptera. 377
omissions of described species, as well as occasional inaccu-
racies in the description of the venation, hardly to be expected
from so careful a worker.
Unfortunately the concluding portion of the paper on the
Acophoridz has not yet reached me, and | am in consequence
obliged to omit one or two species, the genera of which I
believe I succeeded in identifying by the introductory tables.
In conclusion, 1 must express my thanks to Lord Walsing-
ham for kindly allowing me to examine the Australian Micro-
lepidoptera in the Zeller collection, as well as a small number
of specimens received from Mr. Meyrick.
Unless where otherwise stated, single specimens only of each
species were received.
RHOPALOCERA.
Lycenide.
IALMENUS, Hiibn.
(918.) Lalmenus evagoras, Donov.
Lalmenus evagoras, Donov. ins. New Holl. t. xxx. fig. 1 (1805).
(919.) Lalmenus ictinus, Hew.
Lalmenus ictinus, Hew. Il. D. L. p. 54. n. 2, t. xxiv. figs. 6-8.
Lycana, Fabr.
(707.) Lycena merens.
Closely allied to ZL. erénus, Fabr. (Don. Ins. N. Holl.
pl. xxxi. fig. 3), but smaller and much darker. The wings
of a dull greyish black, the blue being pronounced only on
extreme base of fore wings and upon abdominal area of hind
wings. Underside cinereous, differing from erdnus (1) in the
enlargement of the lower three instead of two of the submar-
ginal row of spots; (2) in the presence on the apical region
ot the hind wing of a large irregular blackish-grey subapical
blotch ; (3) instead of the series of sagittate markings of
erinus, the wings are traversed by three distinct parallel rows
of blackish dots ; (4) fringes white-spotted, resembling Holo-
chila anita, Semper (Journ. d. Mus. Godeftroy, xiv. p. 163).
Lucia, Swains.
(831.) Lucia ? pyrodiscus.
Lucia ? pyrodiscus §, Newm. MS. in B. M,
Brownish black, with a reddish-purple tinge.
378 Mr. R. Rosenstock on Australian Lepidoptera.
Fore wings with the disk deep fiery golden metallic: hind
wings duller brownish golden-yellow, without metallic sheen
on the submedian area; fringes whitish grey, with a blackish
~ basal line, in the hind wings wrorated with brownish yellow.
Underside.—Pale whity brownish café-au-lait colour, with
a series of dark fuscous paler whitish-margmed markings,
cordiform (in outline), and disposed in transverse rows across
the wings ; two deep chocolate-brown semilunar spots on anal
angle of hind wings, continued anteriorly by a row of similar
but very much fainter submarginal spots, hardly distinguish-
able on the fore wings; head, palpi, thorax, and abdomen
blackish brown above, whitish beneath ; antenne alternately
black- and white-ringed, the clubs black, brownish red at
tips and underneath.
I have referred this species to the genus Lucia. Butler,
followed by Semper, places it and the allied species /émbaria,
Swains., =aurifer, Blanch., under Zeritis ; but I fail to see any
resemblance to Boisduval’s type of that genus (4. neriene
(Guinea), Boisd. Sp. Gen. pl. xxii. fig.6). The venation, too, of
Zer itis, as represented in Boisduval’s figure, is entirely different
from what I observe in my species, which, on the other hand, in
this respect perfectly agrees with Lucia limbaria. In Zeritis
three subcostal branches are emitted from beyond the angle of
the cell, while only one radial vein, presumably the lower, is
figured. In limbaria and aurifer two subcostal branches only
rise from a common stalk, emitted from the angle of the cell,
while an upper radial vein issues from the same point, and
the lower radial is emitted at the middle of the discocellular
veins.
Hesperide.
PAMPHILA, Fabr.
(884.) Pamphila lascivia, n. sp. (Pl. XI. fig. 1.)
Golden brownish black ; palpi with basal and second joints
covered with whitish-yellow hairs; terminal joints black,
naked; thorax and abdomen black, with deep olivaceous
yellow hairs above, pale olivaceous whitish beneath; anal
tuft deep yellow-ochreous.
Upperside.—F ore wings: inner two fifths of costal margin,
interior of cell, first, second, and third subcostal branches
bordered with deep golden yellow, anda submarginal band of
six orange-yellow spots. Hind wings with a transverse band
of oblong deep golden-yellow spots, starting from below costa
near apex, and directed towards middle of abdominal margin,
which, however, it does not reach. :
Mr. R. Rosenstock’on Australian Lepidoptera. 379
Under surface.—Fore wings: costal border, apical region
deep yellow ; rest of wing brownish black ; submarginal spots
as above. Hind wings yellow ochreous, with a faint longitu-
dinal brownish-black stripe, attenuated above, parallel to
abdominal margin.
Expanse of wings 25 millim.; length of body 13 millim.
TRAPEZITES, Hiibn.
(412.) Trapezites symmomus, Hibn.
Trapezites symmomus, Hiibn. Zutr. ex. Schmett. figs. 225, 226.
(828.) Zrapezites vacchus, Fabr.
Pap. iacchus, Fabr. Syst. Ent. p. 533. n. 889; Donoy. Ins. New Holl.
t. xxxi. fig. 1.
TELESTO, Boisd.
(829.) Telesto ornata, Leach.
Hesp. ornata, Leach, Zool. Misc. i. p. 126, t. lv. figs. 4, 5.
(830.) Telesto donnysa, Hew.
Telesto donnysa, Hew. Descr. Hesp. p. 39. n. 3 (1868).
(726.) Telesto Doubleday?, Feld.
Telesto Doubleday?, Feld. Verh. zool.-bot. Ges. xii. p. 491. n. 180 (1862) ;
Herr.-Schatf. Ex, Schmett. fig. 112.
(393.) Telesto scepticalis, n. sp. (PI. XI. fig. 2.)
Golden brownish black ; head, thorax, and abdomen deep
black above, covered with greenish yellowish white hairs
below; antennal joints black, ringed with yellow above,
below yellow, club black, below reddish brown; palpi,
front of thorax, and anterior part of upperside of abdomen
covered with intermingled blackish and olivaceous hairs; anal
tuft brownish ochreous.
Upper surface.—Basal region of both wings covered with
deep yellow hairs; fore wings with an irregularly oblong
yellow discocellular mark ; three connected small pale yellow
subcostal spots at about three fourths length of wings, two
larger well-defined yellow spots obliquely in front of and below
discocellular spot, and a small sagittate spot below these a
little above and beyond middle of hind margin. Hind wings
with a single large yellow oblong discocellular spot. Fringes
all deep yellow, alternately mixed with black.
Underside.—F ore wings: costal region and upper portion of
wing brownish ochreous ; rest of wing blackish, except at inner
380 Mr. R. Rosenstock on Australian Lepidoptera.
margin, which is olivaceous yellow ; upper two thirds of outer
margin bordered by a greyish-blue (glaucous) elliptical patch.
Hind wings reddish brown, clouded with greyish blue, with
a paler, whity-brown, broad, angulated median band, not
reaching costa or hind margin, and bordered anteriorly and
posteriorly by a row of grey-blue deeply brown-ringed inter-
neural spots, those of the inner row fainter and less distinct.
EXxpanse of wings 264 millim.; length of body 14 millim.
HETEROCERA.
Hepialide.
Three much worn specimens only have come to hand, the
species being quite undeterminable.
Two specimens (635) are apparently male and female, per-
haps of Fratis simulans (Stephens, MSS., Walk. Cat. vu.
p- 1564).
The other specimen (365) is much larger and also a Frais.
Cossidee.
Cossus, Fabr.
Cossus ligatus, Walk.
Cossus ligatus, Walk. B, M. Cat. L. H. Suppl. ii. p. 585.
Also a much worn specimen.
Castniide.
SyNemon, Doubl.
(724.) Synemon hesperioides, Feld.
Synemon hesperiotdes, Feld. Novara Heterocera, pl. lxxxii. fig. 12.
Agaristide.
AGaristA, Leach.
(206.) Agarista affinis, Boisd.
Agarista affinis, Boisd. Voy. de l’Astrolabe, pt. i., Lep. p. 177.
Zygenide.
SynTomMIs, Ochs.
(424.) Syntomis aperta 9, Walk.
Syntomis aperta 9, Walk. l. c. Suppl. i. p. 72.
Mr. R. Rosenstock on Australian Lepidoptera. 381
Lithosiide.
Asura, Walk.
(220.) Asura cervicalis, Walk.
Asura cervicalis, Walk. J. c. ii. p. 484.
Kurang, Walk.
(290.) Hutane lydia, Donov.
Lithosia lydia, Donov. Ins. New Holl. pl. xl. fig. 1.
TIGRIOIDES, Butl.
Tigrioides, Butl. Trans. Ent. Soc. 1877, p. 359.
(763.) Tigriotdes transversa §, Walk.
Inthosia transversa, Walk. 1. e.
Walker describes a single female. I have little doubt
that no. 763, which is rather rubbed, is the male of this
species; the markings agree perfectly. Herrich-Schiffer’s
Lithosia histrionica (Hixot. Schmett. fig. 440) is a synonym of
Butler’s type of the genus (Setina alterna, Walk.).
TEerMEssA, Walk.
(274.) Termessa leta, Walk.
Termessa leta, Walk. 1. c. vii. p. 1689.
Mosopa, Walk.
(618.) Mosoda anartoides, Walk.
Mosoda anartoides, Walk. 1. c. Suppl. v. p. 1899.
(445.) Mosoda consolatrix, n. sp.
This species closely resembles Halone sobria, Walk., Natal.
I failed to detect any essential generic differences between the
latter genus and Mosoda.
Head, antenne, thorax, and abdomen greyish fuscous;
hind tibize pale whitish ochreous, naked, with four spines.
Fore wings greyish brown, irrorated with whitish grey, and
with some obscure indefinite dark brownish maculate bands.
Hind wings stramineous yellow ; apex suffused with greyish
fuscous.
A worn specimen. Expanse 22 millim.
(224.) Mosoda jocularis 8,n. sp. (PI. XI. fig. 6.)
Head black, with lateral white spots; antenne strongly
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 26
382 Mr. R. Rosenstock on Australian Lepidoptera.
pubescent, dark fuscous; palpi obliquely ascendant, black ;
proboscis strong, reddish amber-coloured; thorax greyish
black, with lateral patches of white scales; collar white;
tegule blackish, edged with long whitish hairs; legs dark
greyish, hind tibie and tarsi yellow ; abdomen deep yellow,
smoky black near base.
Fore wings white, yellow-tinged along hind margin, with a
falciform blackish basal mark commencing upon costa, but not
reaching hind margin; a black transverse line from costa at
two fifths of its length, attenuated posteriorly ; a well-defined
black circular discocellular dot, with a small blackish costal spot
above and an indistinct sagittate mark below ; an irregular
submarginal band with outward angular projections abutting
upon the narrow, blackish, hind marginal border.
Hind wings pale stramineous yellow; apex suffused with
black, and a small blackish discocellular spot.
Expanse of wings 20 millim.; length of body 7 millim.
PHILENORA, nh. g.
Antenne of male strongly pectinated ; palpi short, clothed
with appressed hairs, porrected, hardly projecting beyond
head; face obtusely conical; proboscis strong; thorax sub-
ovate, moderately convex, with promiment collar and short
side tegule ; abdomen slender, not extending beyond hind
wings in male, with strong anal tuft. Fore wings subtrian-
gular, with rounded apex, oblique outer and slightly simuate
inner margins.
Allied to Mosoda, Walk., but differing in the strongly
pectinated antennee, which are merely pubescent in the latter
genus, and in the neuration of the fore wings, vein 10 (second
subcostal branch) being emitted at upper angle of cell from
same point as 9 and the common stalk of 7 and 8, and 11 from
the anterior fourth of the cell; whereas in Mosoda 10 rises
from the subcostal from before the angle of the cell, and 11
behind it from posterior third to half of cell.
(18.) Phelenora undulosa g, Walk.
Acontia undulosa, Walk. @. ¢. xii. p. 797.
Walker wrongly described the female of this species as an
Acontia. I was therefore obliged, in the absence of any other
corresponding Lithosiid genus, to create a new one for its
reception.
The male of this species, besides difference of antennal
characiers and smaller size, has the white ground-colour of the
fore wings somewhat obscured by grey, rendering the trans-
verse markings fainter. Expanse 22 millim.
Mr. R. Rosenstock on Australian Lepidoptera. 383
Liparide.
Evproctis, Hiibn.
(228.) Huproctis obsoleta g , Fabr.
(354.) Huproctis obsoleta 2 , Fabr.
Bombyx obsoleta, Faby. Syst. Ent. p. 579. n. 77 ; Donov. Ins. New Holl.
pl. xxxv. fig. 1.
Inparis obsoleta, Boisd. Voy. de l’Astrolabe, pt. 1, Lep. p. 218.
THALAINA, Walk.
(650.) Thalatna inscripta, Walk.
Thalaina inseripta, Walk. 1. ¢. iii. p. 661.
Plusargyria principiaria, Herr.-Schaff. Exot. Schmett. fig. 440,
Walker’s description was published in 1855; Herrich-
Schiffer’s figure appeared in 1856, and his name is therefore
a synonym.
Lerna, Walk.
Lerna nivosa, Walk.
Lerna nivosa, Walk. 1. c. Suppl. ili. p. 805.
Placed by Walker among the Anthophilide, but undoubt-
edly a Liparid.
Epricoma, Hubn.
Marane, Walk. 1. c. Suppl. ii. p. 397.
Epicoma pontificalis 2 , n. sp.
Closely resembles Hpicoma contristis, Hiibn. Zutr. ex.
Schmett. 111. figs. 217 and 218, but differs (1) in the outer border
of the yellow discal suffusion on the under surface of the fore
wings being quite straight instead of notched in the middle ;
(2) in the absence on the under surface of the hind wing of a
yellow submarginal band inside of the yellow border (in this
character it agrees with Bombyx tristis ? , Lewin, Lepid. Ins.
N.S. Wales, pl. vii. fig. 4, in which, however, this band is
absent on the front wing also); (3) in the abdomen having
only a single yellow spot placed on the middle of the dorsal
surface.
Sitina, Walk.
(420.) Sctina, sp.
A much worn and quite undeterminable specimen.
26*
384 Mr. R. Rosenstock on Australian Lepidoptera.
Sezeris (Cebysa), Walk.
(281.) Sezeris conflectella, Walk.
Sezeris confiectella, Walk. 1. c. xxviii. p. 509.
Described as a Tineid.
Lasiocampide.
OpsIRRHINA, Walk.
(325.) Opsirrhina obscura, Walk.
Lebeda obscura, Walk. J. c. vi. p. 1464.
Two specimens, a male and a female.
PTEROLOCERA, Walk.
(86.) Pterolocera amplicornis, Walk.
Pierolocera amplicornis, Walk. 1. c. iv. p. 889.
Cotussa, Walk.
(269.) Colussa simplex, Walk.
Darala simplex, Walk. 1. c. iv. p. 891.
(217.) Colussa basigera, Walk.
Darala basigera, Walk. 1. c. Suppl. ii. p. 372.
Darala undulata, Feld. Novara Het. pl. xcviti. fig. 11.
(56.) Colussa vinosa, n. sp.
Purplish vinous red, irrorated with black and ochreous
yellow. Head, palpi, and thorax dark sienna-red; antennz
pale-grey whitish; legs pale yellowish grey, speckled with
greyish black.
Upperside.—F ore wings with the submarginal area densely
irrorated with ochreous yellow, and with two faint, parallel,
punctiform, submarginal, zigzag lines. Two black punctiform
discal spots, an inner one within the cell, and an outer
one upon the middle of the discocellular vein. Hind wings
somewhat paler than fore wings, with markings similar ;
abdominal margin with pale reddish-brown hairs; fringes
pale vinous reddish.
Underside.—Paler, with markings on both wings similar,
but more distinct. Expanse 45 millim.
The specimen had no body and was much worn.
Messrs. Etheridge and Foord on Laceripora cribrosa. 385
Nataxa, Walk.
(420.) Natara flavifascia, Walk.
Nataxa flavifascia, Walk. 1. c. v. p. 1179.
Described among Drepanulide, but undoubtedly a Lasio-
campid of the Limacodes group.
[To be continued. |
XXX V.—WNote on Laceripora cribrosa, Hichwald. By
Ropert ETHERIDGE, Jun., and ARTHUR H. Foorp, F.G.S.
WE desire to make a correction in the name of the genus to
which we assigned Laceripora cribrosa, Hichw.* It was de-
scribed in our paper asa Chetetes; but Prof. H. A. Nicholson,
who has recently returned from Esthonia, Russia, has brought
a number of specimens of it, sections of which show incon-
testably that it is not a Chetetes, but a highly perforated
Favositoid Coral. We are of opinion, moreover, that Hich-
wald’s generic name should be retained. ‘The sections which
were prepared to illustrate our paper showed no trace of
mural perforations, owing, in a great measure, to the unsatis-
factory state of preservation of the only examples available
at the time. The accompanying woodcut shows the true
characters of this interesting form, as seen in a vertical section.
In this the unusually large size of the mural pores is apparent,
and they impart that peculiar appearance to the cells which
* This Journal, Noy, 1884,
386 Mr. G. A. Boulenger on
was shown in the transverse section (1a) given in our plate,
and which led Eichwald to adopt the term Laceripora for
his genus. The structures described by us as “ incipient
divisions of the cells” are thus accounted for.
Dr. Lindstrém’s later views, as quoted in our paper, are
therefore quite acceptable, viz. that Lacertpora should be
retained as a distinct genus of the Favositide ; and in this
opinion Dr. H. A. Nicholson also concurs.
XXNXVI.—Remarks on Mr. C. W. De Vis’s recent Contri-
butions to the Herpetology of Australia*. By G. A.
BOULENGER.
Ir is painful to have to record such contributions as Mr.
De Vis’s herpetological papers, but it is a duty for the
working zoologist, who constantly complains of the plague
of synonymy, not to allow them to pass without protest.
Their author is no doubt stimulated by the desire of promoting
herpetological knowledge in his country, but, through his
incompetence and want of care, he will do much harm. As
regards certain groups of Reptiles he may, in defence,
point to the great difficulties attending these studies owing
to the absence of general treatises; but when he has in his
hands the recent ‘Catalogue of Batrachians in the British
Museum,’ and is not even able to distinguish a Rana from a
Hyla, or to recognize so striking a form as Mixophyes, he has
no excuse, and one can only wonder at his daring to write on
subjects of which he is so manifestly ignorant.
The papers in question contain descriptions of no less
than thirty new species, several of which are made the
types of new genera. I have no time at present to go through
the whole of them, and must restrict my remarks to the groups
which I have fully worked out, viz. the Batrachians and the
Lizard-families Geckonide and Agamide. Mr. De Vis’s
additions to those groups amount to fifteen new species, which
are enumerated below. Of these, three appear to deserve
recognition, one is doubtful, the rest are synonyms of species
previously named.
1. Limnodynastes lineatus (Proc. Linn. Soc. N. 8. W. ix.
1884, p. 65) = L. Peronit (D. & B.).
* Proc. Linn. Soc. N.S. Wales, ix. 1884, and Proc. Roy. Soc. Queensl.
i, 1884-85.
the Herpetology of Australia. 387
. Limnodynastes olivaceus (1. c. p. 66). A good species.
3. Hyla Rothii (1. c. p. 66) = A. Peroni, Bibr.
Of these three species, type specimens are now in the
Natural-History Museum, through the kindness of H.
Ling Roth, Esq.
. Gdura Tryon (Proc. R. Soc Queensl. i. p. 54, 1884) =
@. ocellata, Bouleng. Cat. Liz. i. p. 105, pl. 1x. (1885).
Although very imperfect the description 1s recognizable,
and as the name Zryoni has priority that of ocellata must
be cancelled.
. Amphibolurus branchialis (l. c. p.55) = Physignathus Lesu-
eurtt, Gray (figured in Dum. & Bibr. Erp. Gén. pl. xl.
and in McCoy’s Prodr. Zool. Vict. dec. ix. pl. Ixxxi.).
. Macrops (g.n., a name already applied to three different
genera in zoology) nuchalis (J. c.p. 97) = Amphibolurus
reticulatus (Gray).
. Diporophora nuchalis (1. c. p. 98) = D. australis (Steind.).
. Diporophora ornata (1. c. p. 99) = D. australis.
9. Diporophora brevicauda (1. ¢. p. 99) = D. bilineata,
Gray.
. Diporophora pentalineata [!] (lc. p. 99) = D. bilineata.
. Hyla fenestrata (1. c. p. 128) = Mixophyes fasciolatus,
Gthr. (figured in P. Z. 8. 1864, pl. vii.).
. Hyla trrorata (1. ¢. p. 128). Should be compared with
H, infrateniata, Gthr.
. Hyla nobilis (1. c. p. 129) = Rana papua, Lesson.
. Hyla peninsule (1. c. p. 129) = H. nasuta (Gray).
. Gidura fracticolor (l. c. p. 160). Apparently a distinct
species, if referred to the correct genus.
I take this opportunity of changing the name 4lurosaurus,
which J employed for a genus of Geckos (Cat. Liz. i. 1885),
but which is preoccupied by a Theriodont (4¥lurosaurus,
Owen, 1881), to that of dluroscalabotes. I am obliged to
my colleague Mr. Smith Woodward for calling my attention
to
this matter.
388 Mr. G. A. Boulenger on
XXXVIL—A List of Reptiles and Batrachians from the
Island of Nias. By G. A. BOULENGER.
TE following list is based on several collections recently trans-
mitted to the Natural-History Museum by Dr. M. Schreiber.
The collector is Hr. Sandemann. ‘The herpetological fauna
of Nias has already formed the subject of a paper by Dr. J.
G. Fischer +, who enumerates twenty-two Reptiles and three
Batrachians. ‘Twenty-seven Reptiles and six Batrachians are
recorded below, of which eleven of the former and four of the
latter (preceded by an asterisk) are not mentioned in Fischer’s
list. On the other hand, the following species recorded in the
latter have apparently not reached us:—Gehyra mutilata,
Wiegm.; Tiliqua sulcata, Ptrs.; Tiliqua percarinata, Ptrs. ;
Ablabes ornatus, Schleg.; Ablabes baliodirus, Schleg.; Cal-
lophis flaviceps, Cant.; and Rana chalconota, Schleg. The
snake described by Fischer as Simotes afjinis, sp. n., I identify
as S. labuanensis, Gthr.; and his Zrimeresurus erythrurus,
Cant., var., I suspect to be 7. formosus, Schleg.
REPTILIA.
*1, Hemidactylus frenatus, D. & B.
2. Gecko stentor (Cant.).
3. Gecko monarchus (D. & B.).
#4, Ptychozoon homalocephalum (Crev.).
5. Draco volans, L.
*6. Aphaniotis fusca, Ptrs.
7. Gonyocephalus grandis (Gray).
8. Calotes cristatellus (Kuhl).
*9. Tiliqua rufescens (Shaw).
10. Xenopeltis unicolor, Reinw.
#11. Calamaria Stahlknechti, Stol.
Three specimens of a Calamaria agree so well in most
respects with Stoliczka’s description of C. Stahlknechti (Journ.
As, Soc. Beng. xlu. 1873, p. 119, pl. x1. fies?) 2 izom
Sumatra, that I can separate them only as a colour-variety.
The lower surface of the body is either uniform yellowish or
+ Abhandl. naturw. Ver. Hamburg, ix. (1885).
Reptiles and Batrachians from the Island of Nias. 389
with distant, ill-defined, black cross bars. Ventrals 147, 148,
150; caudals 23, 22, 22.
#12. Pseudorhabdion longiceps (Cant.).
13. Stmotes labuanensis, Gthr.
*14, Simotes octolineatus (Schn.).
15. Oligodon trilineatus (D. & B.).
16. Tropidonotus trianguligerus, Boié.
17. Tropidonotus chrysargos, Boié.
*18. Hypsirhina albomaculata, D. & B.
#19. Zapyrus fuscus, Gthr.
20. Chrysopelea ornata (Shaw).
21. Dendrophis picta (Gm.).
22. Dendrophis caudolineata (Gray).
23. Dryophis prasina, Reinw.
*24. Ophites subcinctus (Boié).
#25. Ophites albofuscus (D. & B.).
An adult specimen measures 177 centim. Uniform
blackish brown above, white inferiorly. Ventrals 238;
caudals 155.
26. Callophis intestinalis (Laur.).
27. Bothrops formosus (Schleg.).
BATRACHIA.
1. Rana macrodon, Kuhl.
*2. Lana nicobariensis (Stol.).
Hylorana nicobariensis, Stoliczka, Journ. As. Soc. Beng. 1870, xxxix
p- 150, pl. ix. fig. 2.
Very closely allied to R. alticola, Blgr., from which it is
distinguished by the rather longer toes, the length of the foot
nearly equalling that of the tibia. In R&. alticola the foot
measures about three fourths the length of the tibia. A single
specimen, obtained from the stomach of a snake.
#3. Rana erythrea (Schleg.).
#4, Callula baleata (Miill.).
5. Bufo claviger, Ptrs.
*6. Ichthyophis glutinosus (L.).
390 Bibliographical Notices.
BIBLIOGRAPHICAL NOTICES.
A History of British Birds. By Writtram Yarrett, V.P.LS., F.Z.8.
Fourth Edition, revised and enlarged: Vols. J. & Il. by ALFRED
Newron, M.A., F.R.S.; Vols. III. & IV. by Howarp SaunpErs,
F.LS., F.Z.8., &e. (Van Voorst.)
Or the works on ornithology which have recently appeared none
will be hailed with greater satisfaction than the new edition of
Yarrell’s ‘ British Birds, which has recently been brought to a
successful conclusion. The first edition of this standard authority
was completed in 1843, a second and third being subsequently
issued, the last in 1856 : both of them little more than reproductions,
with additions, of the original.
In 1871 the publisher, with a due appreciation of the great
advance which had been made in ornithological knowledge, deter-
mined to bring out a fourth edition of this deservedly popular work,
embodying the information subsequently acquired. In these days,
however, to edit a work of this nature is no mean task, and
requires an ornithologist of the highest ability for its perform-
ance. It is not merely a repetition of previous editions, with
perhaps an editorial footnote here and there, but a careful revision
of the whole that has to be done. LEvery bird’s history has to be
brought up to date; the evidence upon which some of the rarer
species have been—perhaps too hastily—admitted to a place in the
British avifauna has to be carefully weighed, and the claims of
numerous aspirants to the honour minutely sifted. Indeed, owing
to the numerous importations which now take place, the decision
as to whether a bird is a truly wild one or has merely escaped—
in other words, whether it reached this country with or without the
aid of man—is one of the most unsatisfactory duties that can fall
to the lot of an editor. Moreover, the mass of literature that
has to be digested, scattered as it is through numerous publications,
is enough to appal any but the stoutest heart. That this was not
lost sight of is evident from the fact of the work being entrusted
to the first-named editor, than whom no one more competent to
undertake the task could have been found.
Bearing in mind the systems with which the ;.ublic have become
more or less familiar, we think that to have made violent changes
in the arrangement, or in any other material point, would have been
attended with risk of diminishing the utility of the work; and we
therefore consider that in adhering, in the main, to the sequence
of the preceding edition, Prof. Newton exercised a wise discre-
tion. Not that there are no changes; far from it. For instance,
the old-fashioned and non-scientific reader will be astonished to
find that the Swifts (Cypselide) are no longer placed with the Swal-
lows (Hirundinid) nor the Golden Oriole with the Thrushes—the
former having been removed from the Passeres to the Picariz, and
the latter from the Merulide to the Oriolide. These and several
other changes of a similar nature have been rendered imperatively
necessary by the light of modern research. With regard to this
Bibliographical Notices. 391
last-named species, it may be mentioned that while the work was
passing through the press the first authenticated cases of its breeding
in the Isle of Thanet occurred in 1874 and 1875, as recorded in ‘ The
Field’ of those years.
The first two volumes include the Accipitres, Passeres, and Picarie.
There are no very great changes in the first Order, but two species of
the large Northern Falcons are admitted as British in place of
the so-called Gyr-Faleon of former editions; and the Black Kite
(Milvus migrans) is figured and described as a rare visitant—a great
deal of fresh information being added with regard to these and
other species. In the Passeres we find the following additions :—
Muscicapa parva, Lanius minor, Turdus atrigularis, Acrocephalus
aquaticus, Anthus spipoletta and <A. campestris, Melanocorypha
sibirica, Euspiza melanocephala, Emberiza rustica and E. pusilla,
Serinus hortulanus, and Pyrrhula erythrina: all upon evidence that
cannot be disputed, besides additional matter concerning many others.
Not the least startling feature is the amalgamation of the Black
Crow (C. corone) and Hooded Crow (C. corniv) into one species,
regarding which much diversity of opinion exists in ornithological
circles. Another is the elimination from the British list of the
Black Woodpecker (Picus martius) in default of any satisfactory
evidence of the occurrence of that species in the British Islands.
When these two volumes had been finished, Professor Newton
was compelled by circumstances to relinquish the editorship; the
somewhat invidious task of succeeding such an author being, with
becoming public spirit, undertaken by Mr. Howard Saunders, whose
name has long been specially connected with the Laride ; and here,
again, the publisher is to be congratulated on having secured the
services of so able an ornithologist. The two volumes under his
charge—commencing with the Columbide and ending with the
Anseres—comprise some extremely interesting additions to the
British list. Amongst them may be noticed the Sand-Grouse (Syr-
rhaptes paradowus), whose irruptions into these islands in 1859 and
1863 must still be fresh in the memory of all who are interested in
birds; the Great Black-headed Gull (Larus ichthyaétus); the Sooty
Shearwater (Puffinus fuliginosus); the Flamingo (Phenicopterus
roscus), whose strange manner of nesting is depicted in the wood-
eut at the head of the article; and the Snow-Goose (Chen hyper-
boreus). As an instance of the increase of our knowledge it
may be observed that at the date of the last edition the nidifica-
tion of the Black-winged Stilt (Himantopus candidus) was so
impertectly known that Hewitson only tells us that this bird “lays
its eggs upon the ground,” while doubting that it lays as many as
four; and Yarrell does not even commit himself to the former
assertion. Its nesting isnow fully described, and, curiously enough,
it seems that, contrary to the habits of its neighbour the Avocet,
and of the Plovers generally, which lay their eggs in a hollow, this
bird sometimes, although not usually, builds a raised nest—a minia-
ture Flamingo’s in fact—a habit rendered necessary, we imagine,
by the situation selected, on the mud by the margins of lakes.
Amongst the birds which are no longer to be found in this work
392 Bibliographical Notices.
are the Virginian Colin (Ortyx virginianus) and the Barbary
Partridge (Caccabis petrosa), both of them introduced species
which have failed to establish themselves in this country. Any
one who reads between the lines can see that Mr. Saunders,
from his personal knowledge of its habits, is sceptical as to the
genuineness of the recorded occurrences of the Andalusian Hemi-
pode, a species not given to wandering, not found in Malta
or France, and so restricted in its habitat that even in Spain and
Sicily it is only found in certain southern districts. The so-called
“Sabine’s Snipe” is now generally regarded as a melanic variety,
and has been expunged from the list, although the beautiful original
woodcut, remarkable even amongst others for its execution, has
been retained as a tailpiece.
A new illustration is given of the Rosy or Cuneate-tailed Gull; and
there is also one to show the adult plumage of the Pomatorhine
Skua, only the immature stage having previously been figured.
The Masked Gull (Larus capistratus) is no longer considered a
valid species, nor does the editor admit the claims of the American
Laughing Gull (Z. atricilla) to a place in the British list. In the
article on the Fulmar Petrel it is pointed out, for the first time, that
the young birds of the pale form are similar in plumage to the
adults, and that the grey birds, which were formerly supposed to
represent the intermediate stage, are not the young of the above, but
belong to a distinct dark form. The Ringed Guillemot is degraded
from its former specific rank; and it is clear that if Mr. Saunders
had been writing a book entirely his own, such species (admitted by
Yarrell) as the Polish Swan, the Canada, Spur-winged, and Egyp-
tian Geese, and more than one Duck, would have been omitted.
In a short Preface placed at the commencement of the third
volume Mr. Saunders gives his reasons for certain changes in the
systematic arrangement which he considers to be unavoidable con-
sistently with the present state of our knowledge. In former
editions the order Limicole was split in two, the precocial Plovers
being separated from the equally precocial Snipes, Sandpipers, &c.
by the Herons &c., whose young are helpless for some time after
they are hatched; the Phalaropes were placed next to the Rails,
and the whole of the above and some other genera were comprised
in one huge impossible Order—Grallatores. The Gulls and Terns,
now admitted to be so closely allied to the Limicole that it is
doubtful whether they ought not to form part of that order, were
classed with Ducks &c. as Natatores; and the Petrels, now known to ©
have little in common with the Gulls but a superficial resemblance,
were actually placed among the Laride! All this is now altered, and,
as we believe, very much for the better, although there will doubtless
be some grumblers who will not take the trouble to refer to the
capital index, and complain that they “never know where to look
for a bird now.”
The entire work has been so thoroughly well executed that we have
no hesitation in stating that it will maintain its place as the standard
Bibliographical Notices. 393
book of reference on British birds, alike on the book-shelf of the
student and in the library of the country gentleman, for many years
to come.
Russian Central Asia. By Henry Lanspett, D.D. In two volumes.
8vo. London, 1885. |
Zooxoeists will experience much satisfaction in finding in a work,
the author of which does not claim to be a naturalist, unexpectedly
a source of information which is all the more welcome as it refers to
a part of the globe that claims our attention in an unusual degree.
We sadly, missed in Dr. Lansdell’s first work, ‘Through Siberia,’
information as to the natural productions of that remote region,
and could not help feeling that an opportunity had been lost. This
is in some measure remedied in this new work on Russian Central
Asia. It forms two large volumes, handsomely illustrated with
seventy engravings and maps.
The bulk of the work is occupied by the author’s record of his
journey of 12,000 miles through Western Siberia to Kuldja, thence
through the Kirghese steppes to Tashkend, Khokand, and Samar-
kand. Crossing into Bokhara he travelled to the Oxus, down which
he floated 300 miles to Khiva, and then continued by a new route
across the land of the Turkomans and north of Merv to Krasnovotsk.
As province by province of Russian Central Asia are described, their
several faunas and floras are shortly characterized; but the most
important part of the information is contained in the appendices at
the end of the second volume, which extend to about 150 pages of
closely but clearly printed matter.
Concerning the fauna of Russian Turkestan Dr. Lansdell, after
pointing out that until within the last thirty years Turkestan was
all but unknown to science, gives a brief account of the various
naturalists who have proceeded there—amongst whom the first
place is very properly given to Professor A. P. Fedchenko, whose
work, written in Russian, is unfortunately a closed book to the
majority of English naturalists.
Thanks to help which Dr. Lansdell has received, the introductions
to the various portions of Fedchenko’s collection are translated and
supplemented by lists of the species, so that the English reader may
obtain a good idea of the fauna and flora of the region traversed.
Severtzoff’s lists of mammals and birds had already been translated,
and to these Dr. Lansdell adds those of reptiles and amphibians,
giving here, as also with the mammals and birds, both the vertical
and horizontal distribution.
We have next the monograph on Turkestan fishes by K. F.
Kessler. In the account of the Mollusks the area is extended
beyond Turkestan to the Altai, the Trans-Baikal, Afghanistan, Tibet,
Cashmir, North-west Himalayas, and Yun-nan. Five pages are
devoted to Arachnida, with 146 species, after which follow the Crus-
taceansand Coleoptera. At the end of this last order Dr. Lansdell
394 Bibliographical Notices.
gives a portion of Solsky’s third part, which was not published
at the time of that author’s death.
The tables on Hymenoptera and Lepidoptera are particularly full,
and to each species is added its distribution in other countries and
its vertical distribution in Turkestan. M. Alpheraky, of Taganrog,
has furnished Dr. Lansdell with a list of 377 species of Lepidoptera
he captured in the Kuldja valley, giving the altitude at which each
species was taken and the month of capture. The remaining lists
contain Neuroptera, Orthoptera, and Vermes.
It should be added that these lists respectively have been revised
for the most part by their authors, or, rather, those of them who
are living; and Madame Fedchenko, who edited so many of her
husband’s works after his lamented death, has also revised'the tables
in their English dress,
A separate appendix is devoted to the flora of Russian Turkestan,
and comprises 1234 plants ; whilst a third consists of a most valuable
bibliography of 700 publications on that region in English, French,
German, Russian, and other languages.
Dr. Lansdell has been too successful a traveller to resist long the
temptation of invading other regions of the east. We understand
that the last sheet of his work had hardly been passed through the
press when he started again for Asia Minor; and we have no doubt
that this new journey will contribute not only to our information,
but also to our collections.
Our Insect Enemies. By TuozoporE Woop. Small 8vo. London:
Society for Promoting Christian Knowledge. 1885.
Mr. Woop has followed up his little book on ‘ Our Insect Allies,’
which we noticed just a year ago, with asimilar volume on injurious
insects. The view of the real nature of the relativns of insects,
whether injurious or beneficial, to man, which we indicated as the
guiding principle of the author in discussing these matters, is still
further developed in his present work, in which he describes the
structure and natural history of a select few of those insects whose
existence acquires prominence by the mischief they cause to us.
The little histories are told in a pleasant style, and in his two books
the author has certainly furnished an excellent popular contribution
to entomological literature, and one which may serve as a valuable
guide in the first steps to a knowledge of the economy of the insect
world. The principal mistake he has fallen into is his devoting
nearly a quarter of his present volume to the natural history of the
Aphides, a subject which, although most interesting to the ento-
mologist, can hardly have its full importance realized by the beginner,
while its occupying so much space has evideutly led to some other
sections of the work being somewhat starved. The volume is
illustrated with a good many woodcuts, mostly of pretty good
quality.
Miscellaneous. 395
MISCELLANEOUS.
A Classification of the Sponges. By Professor Sortas, D.Sc.
Tue Porifera are a distinct phylum (Parazoa) of the animal
kingdom, divisible into two classes, namely :—
I. Plethospongize (7AjO0s, a crowd).
II. Calcispongiz.
The Plethospongie may be subdivided into three orders :—
i. Hexactinellide.
11. Demospongiz (djm0s, the common people).
ili. Myxospongie.
The Demospongiz embrace the great majority of sponges, and
are divisible into two suborders, the Monaxonide and Tetractinel-
lide. The horny sponges may be added as a third suborder, the
Cerospongie ; but since they are probably of polyphyletic origin,
derived from different families of the Monaxonide, it is open as an
alternative to distribute them among the families of that group.
On the Pelagic Annelides of the Bay of Algiers.
By M. C. Vievrer.
From November 1884 to June 1885 I made daily investigations
at the entrance of the port of Algiers, for the purpose of studying
the pelagic fauna of the bay, and especially the Annelida.
It is well known that the pelagic Annelida are divided into
several groups. Some, like the Heterenereids or Syllidiew, without
alternate generations, only belong to the surface-fauna during the
short period of sexual activity. Others are pelagic during their
whole existence; but this existence, which is very short, only
represents the same period of activity as in the preceding group; they
are the sexual stolons of the Sylidizv with alternate generations,
the Polylostricht and Saccoreneides. Lastly, a third group includes
essentially pelagic creatures which have never been observed except
at the surface, and appear to be completely adapted for that mode of
life. From my observations all these organisms belong to the two
families Alciopize and Phyllodociz, for we can only regard as very
greatly modified Phyllodociz, on the one hand Yomopteris, and on
the other the curious Sagittelle. Considering the close affinity
which exists between the families Alciopiz and Phyllodocie, which
were formerly confounded, one might be surprised that all the
animals composing the former being pelagic, there was only known
with certainty a single pelagic Phyllodocian, namely Hydrophanes
of Claparéde. For good reasons I do not mention Lopadorhynchus,
Grube. Three other types of this family had, however, been seen,
396 Miscellaneous.
as long ago as 1879, by M. Greeff, at the Canaries ; but an imperfect
study of them led that naturalist to refer two of them to the Syl-
lidize and one to the Lycoridiz. I have again found not only Clapa-
réde’s Hydrophanes, but also Greeff’s three types ; and, besides these,
two new genera, which also very evidently belong to the Phyllo-
dociz. This makes a total of six genera, presenting a regular
gradation in the concentration of the postcephalic segments and the
arrangement of their appendages.
Among the Alciopiz I have only met with two new species.
As to the animals the like of which inhabit the surface only
during the larval life, and descend to the bottom during the rest of
their existence, it becomes difficult, when one meets with them in
a certain state of development, to say whether they are examples
belated in their pelagic existence, but which finally dwell at the
bottom, or organisms which have definitively adapted themselves to
conditions of existence quite different from those of the rest of the
family. The question can hardly be solved when we do not find
well-developed sexual products. It is in this doubtful class that I
shall range Ophryotrocha, Claparéde, although the Genevese natu-
ralist saw it loaded with ova. In it I shall also place a Polynoé, to
which I for the present abstain from giving a name, but which
appears to me to present a real adaptation to pelagic life.
The following is the complete list of the species observed :—
Aphroditeze :—Polynoé, sp. ?
Lumbriconereides :—Ophryotrocha puerilis, Clap. & Meczn.
Syllidize :—_-A. Without alternate generations: Hvogone gemmifera,
Pag.; Spherosyllis pirifera, Clap.; S. hystrix, Clap.; Grubea
limbata, Clap.
B. With alternate generations: Autolytus?, Virchowia cla-
vata, Langerh.; and several undetermined Sacconereids.
Phyllodocize :—Pelagobia longocirrata, Greeft ; Maupasia ceca, C.
Vig. ; Hydrophanes Krohn, Clap. ; Pontodora pelagica, Greeff ;
Toda microceros, C. Vig.; Phalacrophorus pictus, Greeff.
Alciopiz :—Asterope candida, Clap.; Aleiope Cantraini, Clap. ;
A. microcephala, C. Vig.; Vanadis heterocheta, C. Vig.; Rhyn=
chonerella capitata, Greeff.
Tomopterie :—Tomopteris Kefersteinii, Greeff; Sagittella Kowalew-
skyi, N. Wagn.
It is to be remarked that of these twenty species, four are new,
five have hitherto only been noticed at the Canaries by M. Greeff,
and one at Madeira by M. Langerhans.— Comptes Rendus, Sept. 7,
1885, p. 578.
On the Organization of Truncatella. By M. A. VaysstERE.
The author, somewhat erroneously, says that the genus T’runca-
tella has hitherto been generally regarded as a Pulmonate Gastero-
pod, and the only writers to whom he refers as holding a contrary
Miscellaneous. 397
opinion are Lowe and Clark. But most recent naturalists place
Truncatella among the Branchiferous Mollusca. The author has
obtained specimens of Truncatella truncatula from the Gulf of Lyons,
and describes its general organization and especially its mode of
respiration. :
By earefully crushing the shell and then tearing to pieces the
anterior part of the animal the author displayed an elongated organ,
composed of from twelve to fifteen triangular lamelle covered with
long vibratile cilia. This organ, whichis a true branchia, is attached
to the roof of a large respiratory cavity observed at the dorsal sur-
face of the mollusk. It is placed transversely to the axis of the
body, and its lamellz can be moved by the animal simultaneously or
separately for the renewal of the surrounding water. The mollusk
can store up a certain quantity of water in its respiratory cavity,
which enables the animals to remain a long time out of the water.
The author describes the principal points observed by him in the
anatomy of Z'runcatella. In front of the buccal bulb there is a long
proboscis, which may be employed to assist in locomotion, although
the foot is usually the sole organ of progression. In the buccal
bulb there are two horny jaws, and between them a very long
radula, of which the dental formula is 2, 1,1, 1,2. 'The stomach
is also furnished with horny pieces serving to complete the tritura-
tion of the food. The liver occupies the truncated extremity of the
shell (about the last two whorls) and is large; it discharges itself
by a single duct, which opens into the intestine just behind the
stomach.
The genital gland (male or female) is placed immediately in front
of the liver, to which it always adheres more or less. The excre-
tory duct (deferent canal or oviduct) runs along the right side of
the body, following the intestine, and opens into the respiratory
cavity near the anus; in the male it terminates in a long, eylin-
drical, unarmed penis. More or less enveloping the intestine and
genital duct are various glands (the organ of Bojanus and _ prostate
or albumen-gland); but these could not be separated on account of
the small size of the animals.
The nervous system consists of an cesophageal collar with two
voluminous centres placed above the cesophagus and almost joined
together, the cerebroid ganglia ; two inferior or pedal ganglia, nearly
as large as the preceding, to which they are attached by two con-
nexions on each side, and to each other by a long commissure; and
four much smaller visceral ganglia, placed two and two at the sides
of the cesophagus and only united to the supra-cesophageal centres,
complete the collar. The visceral ganglia are united by two long
connexions with a fifth centre, the viscero-genital ganglion, which
is buried in the glandular mass surrounding the intestine. Besides
these nine centres there are the buccal ganglia, placed at the poste-
rior part of the bulb, below the origin of the cesophagus. The eyes
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 27
398 Miscellaneous.
occupy the basilar region of the tentacles; the otocysts rest upon
the pedal ganglia and are united to the cerebroid ganglia by two
very delicate nerves. Each otocyst contains a single large spherical
otolith.
The author, in conclusion, notices a singular Vorticellidan Infu-
sorian of the genus Scyphidia, which oceurred on the extremity of the
copulatory organ of several of his Truncatelle. The species of this
genus have hitherto been known onlyfrom fresh water ; to this marine
species he gives the name of Seyphidia Fischeri. It has a cylin-
drical body, slightly attenuated above; its peristome is not much
reflexed ; and it has a broad and very thick foot, enabling it to
adhere strongly to the bodies on which it occurs. Its surface is
slightly striated in the direction of its length. These Infusoria move
very slowly.— Comptes Rendus, Sept. 7, 1885, p. 575.
On the Development of Aurelia aurita and Cotylorhiza borbonica.
By Dr. A. Gorrn.
The first segmentations of the ovum produce neither exclusively
equal nor exclusively unequal blastomeres, but the two occur pro-
miscuously together.
A ceelogastrula with a narrower or wider archenteron and a pro-
stoma always exists; but, so far as I can see, is never produced
by invagination. There is rather in the cceloblastula a perfectly
irregular migration of endodermal cells into the blastocceloma, so
that there originates from it a sterrogastrula of which the endoderm
becomes secondarily exeavated (archenteron) and breaks out (pro-
stoma). By the closure of the prostoma and the development of
cilia on the ectoderm the ccelogastrula is converted into the larva
(planula), which swims along with the vertical (aboral) pole for-
ward and attaches itself thereby.
Before or after the attachment a sacciform invagination of the
ectoderm is produced at the prostomial end (Kowalevsky), and this
becomes the persistent ectodermal esophagus, which breaks through
into the stomach. At the same time the endoderm becomes saccu-
lated in the form of the finger of a glove at two opposite sides be-
tween the cesophagus and the ectoderm ; these first two gastral sacs
are continued downwards like grooves in the wall of the stomach,
two gastral folds being produced there in each case. Between the
two primary gastral sacs a new but broader gastral sac is formed on
each side; and the four sacs surrounding the esophagus at the same
time by their contiguity form four septa, which are continued down-
wards into the gastral folds.
The tentacles grow forth above the gastral sacs, at first one over
each of the primary, and then three over each of the secondary sacs ;
of these latter (8+3) tentacles the four outer ones push forth each
in a septal plane. It is only at a later period that the four quad-
rants become equal in their dimensions and in number of tentacles.
Miscellaneous. 399
The so-called muscles of the Scyphistomes originate neither from
the endoderm nor from the outer wall of the cup, but from funnel-
shaped invaginations of the perioral ectoderm into the interior of
the septa and folds, into which they extend themselves like tubes
and remain hollow. The orifices of these tubes are still present on
the young strobila, so that the first Ephyra appears as the original
oral segment of the Scyphistoma.
Besides the strobila-formation a regular budding of the Scyphi-
stoma occurs ; in Cotylorhiza I frequently saw the bud grow forth
with the foot foremost, so that its last connexion with the parent
animal was at the mouth.
From these observations, made throughout on intact living objects
and upon the finest sections, the following deductions may be
drawn :—
a. The celogastrula of the Scyphomedusee investigated is a
secondary embryonic form, as the gastrulation is effected by the im-
migration of the endoderm into the cavity of the ccloblastula.
6. The Scyphistoma 1s a perfect Anthozoon. In favour of the
close relationship of these two forms only the gastral folds could
hitherto be cited; but these also occur, although imperfectly, in
Hydroids, and therefore were not thoroughly decisive as to this
relationship. The mvagination of the ectodermal esophagus observed
by me and the gastral sacs and septa surrounding it, however, stamp
the Scyphistoma as a true Anthozoon.
c. As the strobila 1s produced only by simple division, and the
Kphyra originates under certain circumstances, even without divi-
sion, directly from the Scyphistoma, every ground for the assumption
of an alternation of generations in Aurelia and Cotylorhiza is re-
moved. The Ephyra, and consequently the Scyphomedusa, is a meta-
morphosed Scyphistoma or Anthozoon, just as the Hydroid Medusa is
a metamorphosed Hydrowd Polyp.—dZoologischer Anzeiger, no. 205,
Oct. 5, 1885, p. 654.
On the Original Fundamental Numbers of Medusce and Echinoderms.
By Witnetm Haacke.
Hackel founds his genealogical tree of the Echinodermata, in
which he adopts the Asterida as the ancestors of the other Echino-
dermata, upon the circumstance that in the Asterida there are
species with a variable number of arms and others with a con-
stantly augmented number, while the same thing does not occur in
the other Echinodermata, those “ worshippers of the number five,”
with the exception of the Ophiurz, which, according to Hickel, are
nearly related to the Stellerida.
I have now to state that I have found four quaternary examples
and one sextenary one in a South-Australian species of the Echinid
genus Amblypneustes. Whether similar specimens have been
400 Miscellaneous.
observed in other species of Echinida or among the Holothurie,
Crinoidea, and Blastoidea I do not know; our textbooks and
manuals give no information upon such questions. But, at any rate,
my specimens prove that the privilege of a variable number of para-
meres is not enjoyed by the Asterida alone.
What conclusions are to be drawn from my discovery with regard
to the genealogical tree of the Echinodermata, is a question which I
only wish to raise here; but my communication of it gives me the
opportunity of calling attention to the insecure foundation of the
above inference of Hickel’s.
With regard to the Meduse we are indebted to Hickel for the
demonstration of the original fundamental number of four, from
which the other fundamental numbers which occur among the
Medusez are to be derived ; and the question therefore presses itself
upon us whether the fundamental number five, which prevails among
the Echinodermata, is not also the original number.
In my memoir upon Hydra (‘ Jenaische Zeitschrift,’ 1880) I have
endeavoured to give an explanation of the original tetramerism of
the Medusee, which I may here confirm by an observation made
some years ago at Kiel. I must refer to the above-mentioned
memoir, the most essential results of which have also been obtained
by other naturalists, and have here only to indicate that the Medusa-
bud of Sarsia tubulosa is so placed with regard to the parent polyp
of Syncoryne Sars that one of the median planes of the young
Medusa fixed by the tentacles of the bud stands perpendicular to the
principal axis of the parent polyp, while the latter coincides with
the other median plane of the bud.
The fundamental number of the quaternary Medusz, at least of
the Craspedota, is therefore causally conditioned by the lateral
budding of the Medusa on the polyp; and it is therefore a question
whether something analogous cannot be demonstrated in the case of
the Echinodermata also, although i in them there can of course be no
question of lateral budding.
In any case the question whether pentamerism is or is not some-
thing primordial in the Echinodermata is still an open one; with
reference to the undoubtedly original tetramerism of the Medusze
one might feel inclined to answer it affirmatively.—Zoologischer
Anzeiger, no. 203, August 31, 1885, p. 505.
PRIMES Sumani Te ce Ce
_ CONTENTS OF NUMBER 95.—Jifth Series.
Pan ig Page
XXX. Critical Observations on Prof. Leidy’s ‘*‘ Freshwater Rhizo-
pods of North America,” and Classification of the Rhizopods in
general, By Surgeon-Major Waxricu, M.D. ............-...4. 317
XX XI. On a Collection of Lepidoptera made at Manipur and on the
Borders of Assam by Dr. George Watt. By Arnruur G. Burier,
ME EAS) OU ein Ey Lise Cate bea ican gece) shah ciao nla arate Seber erin teh ae 334
XXXII. Descriptions of Seu oey from the Neighbourhood of Port
: Phillip Heads, South Australia. By H. J. Carrne, F.R.S. &e.. 347
XXXIII. On an Example of Polymorphism in the te
By Caries Curiton, M.A. (New Zealand). (Plate X.).......... 368
. XXXIV. Notes on Australian Lepidoptera, with Descriptions of
new Species. By Ruporpa Rosrnstocn, B.A. (Plate XI.)........ 376
XXXV. Note on Laceripora cribrosa, Hichwald. By Rozert
Eruerrines, Jun., and Arraur H. Foorp, F.G.8. . Pind iseee ein p ae ee 385
XXXVI. Remarks on Mr. C. W. De Vis’s recent Contributions to.
the Herpetology of Australia. By G. A. Boutunemr ........ »..2 386
- XXXVII. A List of Reptiles and Batrachians from the Island of
Pee tob yey AL MOULENGER \1. Use cs yale ee wae ce eds ra ae 388
BIBLIOGRAPHICAL NOTICES.
A History of British Birds. By Witr1am Yarrutz, V.P.L.S., F.Z.S8,
Fourth Edition, revised and enlarged: Vols. I. & II. by ‘ALFRED
* Newton, M.A., F.R.S.; Vols. III. & IV. by Howarp Saunpers, |
F.LS., F.Z.8., ee Or Ng aia 390
Russian Central Asia. By Henry Lanspert, D.D. .............. 393
Our Insect Enemies. By Tunopore Woop ..... SO eRe RM a 394
MISCELLANEOUS,
A Classification of the Sponges. By Professor Sonnas, D.Sc. ...... 395
On the Pelagic Annelides of the Bay of Algiers. By M. C. Vieurer 2b.
On the Organization of Truncatella. By M.A. Vaysstire ........ 396
On the Development of Aureha aurita and Cotylorhiza borbonica.
Beye tin AL COTTE s/o wire et ic osu Lika arly Neca, 398
On the Original Fundamental Numbers of Menor and Hchinoderms.
By Wirnrm Haackr ........,... TIRES A MGIB ECE NS eran 399
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XXXVIII.—The Victorella pavida of Saville Kent.
By E. C. Bousrrenp, L.R.C.P., Lond.
{Plate XII. figs. 1-3.]
HAvinG recently been so fortunate as to meet with a consi-
derable supply of this beautiful and interesting polyzoon, I
propose in the following notes to give a description of it,
with special reference to the observations of the naturalist who
first found it and described it at some length in the ‘ Quar-
terly Journal of Microscopical Science’ (N.S. vol. x. p. 34,
with pl. iv.). As my own observations differ in one or two
essential points from Mr. Kent’s, I append the systematic
description which he formulated :—
“Family Homodietide.
““ Victorella pavida.
“Polypidom minute, confervoid, adherent or semierect,
irregularly branched. ‘Tentacles eightin number ; no gizzard.
Inhabiting brackish water. Parasitic on the polypary of
Cordylophora lacustris.”
Mr. Hincks, in his ‘ Marine Polyzoa,’ describes the Vécto-
rella, but with important differences from the statements of
Mr. Kent, and, in fact, by combining the two accounts it is
possible to arrive at conclusions somewhat approaching the
truth. Mr. Hincks, however, had not, I believe, the opportunity
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 28
402 Mr. E. C. Bousfield on the
of examining fresh specimens, and his description is but a
portion of what has to be said regarding Véctorella.
I first met with the polyzoon in question last spring, at
which time the zooids were solitary, and semi-repent, colour-
less, and in shape much like a violin with a straight elongated
neck. Not being aware of the observations of Messrs. Kent
and Hincks, I communicated particulars and sketches to one
or two gentlemen who had special knowledge of the subject ;
and Mr. Pennington, of Bolton, first suggested the identity
of my find with Victorella, though its solitary condition and
the remarkable anatomical divergences from published de-
scriptions rendered the identification somewhat doubtful.
I failed to find any further specimens until September,
when I came into possession of a considerable quantity, and
the results of my examination will be embodied in the follow-
ing notes.
The polypidom consists of a series of slender yellow or
brownish tubes, on which at intervals are situated swellings
(fig. 1, a, 6, c), in each of which a zooid is developed in the
ordinary way from an enlargement of the funiculus (fig. 1, d)
or continuous protoplasmic cord which runs through the whole
of the tubes of which the colony is composed. From each
swelling arise two branches at right angles (fig. 1), and by
the growth of these branches and the development of zocecia,
from which again other branches arise, the growth of the
colony continues, always branching in a rectangular direction,
so that a matted mass results. The zooids developed at the
nodal points vary widely in dimensions; I have examined
some which have reached +4; in. in height, whilst others were
not more than - in. At the terminations of the branches are
to be found, as a rule, the largest specimens, and in the case
of these individuals the cell is of much more uniform diameter
than in the smaller ones, so that the whole animal is contained
within it even when retracted.
Taking one of these larger specimens as a type, the follow-
ing appearances present themselves.
The tentacles, eight in number, are arranged around the
mouth of the animal. They are hollow (fig. 2, ¢), and of almost
the same diameter throughout, with the usual row of cilia on
either side. ‘These cilia, however, do not form a continuous
series, but fringe only the adjacent sides of the tentacles, their
place being taken at the apex by a tuft of stiff but very slender
sete (fig. 3,) which are devoid of movement. These sete
extend in a linear series down the outer side of the tentacles,
and specially long ones are also found around the ring formed
by the fusion of the bases of the latter.
Victorella pavida of Saville Kent. 403
The tentacular crown rests upon the upper part of the
pharynx (fig. 2, a, 6, fig. 3,a). This is a pyramidal sac with
thick walls, formed of radiating prismatic fibres, by which it
is rendered capable of great and very rapid dilatation. The
upper margin is thinned out to form the circular lip (fig. 2, 5),
which contains a sphincter muscle, and just below a deep
constriction runs round the outer wall (fig. 2,c). This con-
striction, into which the cavities of the tentacles open, is in
free communication with the perivisceral space below, and
this is the only trace of a vascular system which I have been
able to discover. When contracted the whole of the cavity
within the pharynx, except a small triangular ciliated space
within the mouth, is obliterated, and three radiating folds take
its place. At its termination the pharynx communicates with
the gizzard (fig. 3,6), a slight sphincter-like ring marking
the separation. The possession of a gizzard is denied to
Victorella by Mr. Kent, but its existence is not difficult to
make out with a power of 200 diameters, whilst it is very easy
with anything approaching 400. The point is, moreover, put
beyond dispute by some instantaneous photographs which [
have succeeded in taking with an exposure of 4 second or
thereabouts to magnesium light*.
In these photographs the double sphincter, the upper part
belonging to the gizzard and the lower to the stomach, is
most clearly shown (fig. 3, c).
The gizzard is simply a thin-walled sac, without cilia, but
faintly striated transversely, and showing under a high power
traces of the same honeycomb arrangement as that presented
by the bases of the prismatic fibres of the pharynx. It is
separated trom the stomach by the sphincters just referred to,
and between the two a slight groove exists, marking clearly
the point of separation.
The stomach (fig. 3, d) isa long thick-walled tube, the
lower part of which is of a deep yellowish-brown colour, the
walls showing numerous granules and small oil-globules.
The lower portion of the stomach is continuous by its outer
wall with the funiculus (fig. 3, ¢), which is colourless, and
* These photographs were taken on the Autotype Company’s Chal-
lenge plates, with a camera extended to 8 feet, in order to obtain depth
by the use of a low power. In conjunction with my cousin, Mr. E.
Shepherd, [ am making a series of experiments in this direction, and the
results so far obtained hold out great promise of future success. I look
forward chiefly to being able to obtain accurate outlines of the principal
features, which may, if necessary, be worked up by hand, so as to get rid
of the inexactitude which, to some extent, must always affect the most
finished drawings made by hand and eye alone from living and moving
objects.
28*
404 Mr. E. C. Bousfield on the
passes down to end in an enlargement attached to the wall
of the tube, which is continuous below with the remainder of
the general cord.
The intestine (fig. 3, e) arises from the stomach at a point
opposite to the entrance or cardiac orifice. At the point
where it commences there is within the stomach a semilunar
valve-like flap on the gastric wall, and this, which forms a
pylorus, is ciliated, unlike any other portion of the stomach.
At this point a pellet of food may be seen to be constantly
whirling round in a manner strongly suggestive of the action
of the pellet-forming organ of Melicerta ringens.
The walls of the intestine are thin, and its upper portion
is surrounded by a mass of granular protoplasmic material.
The anus is not, as generally stated, situated immediately
below the tentacles. The intestine terminates halfway
between this point and the stomach (fig. 3, /), and for the.
remainder of the distance a hollow muscular tube passes
upward, and ends at the spot usually assigned to the anal
orifice (fig. 3, 9).
The process of defecation is accomplished as follows :—
The current caused by the reversed peristaltic action of the
stomach drives the flap before spoken of against the cardiac
orifice, thus preventing regurgitation, and the pyloric orifice
opening, the matter about to be rejected is propelled into the
intestine, the pyloric sphincter closing the opening behind it.
The intestine is then drawn up by the muscular tube attached
round the anus, until this last is beyond the membrane which
closes the cell, and the intestine thereupon, and only there-
upon, contracts and expels its contents. ‘The anus then sinks
down to its normal position, until the time arrives for a repe-
tition of the process. ‘This arrangement is so remarkable
that I am glad to be corroborated by the authority of one so
competent as Prof. Allman, who writes :—“ Your remark
regarding the termination of the intestinal tube and its action
in the expulsion of the ejectamenta is interesting, and now
that you have called my attention to it, I think I have
noticed the same phenomenon in other species.”
The whole of the organs are invested by a delicate mem-
brane, which is continued upwards to a point just beyond the
commencement of the tentacles (fig. 2, e), whence it is reflec-
ted on to the inner surface of the tube of the animal. The
tube is composed of a transparent homogeneous substance,
the lower portion being rigid and the upper flexible. The
rigid portion is strengthened at intervals by transverse bars
of a transparent material, free at either end. The flexible
portion is dilated near its centre, and contracts again slightly
Victorella pavida of Saville Kent. 405
towards the point where it joins the operculum (fig. 3, £).
This is a tube composed of a very delicate membrane, deve-
loped independently in a mass of protoplasm at the upper
part of the embryonic cell. It is generally described as com-
posed of sete, around which the membrane is stretched ; but,
whilst I am not prepared to contradict the statements of such
authorities as Professor Allmaz and Mr. Pennington, not to
mention other writers on the subject, I am convinced, after
most careful observation directed to this special point, that
nothing of the sort exists in Vectorella, nor can I find any
trace of setee with the highest power which I have found it
possible to use, about 500 diameters. When seen trom above
the appearance is that of a circular opening, with zigzag
margin, no trace of thickening or unevenness being anywhere
visible. I have also examined specimens of Bowerbankia
imbricata and of Cylindracium without being able to trace
the sete: either with direct or dark-ground illumination, though
the very delicate sete on the tentacles were plainly apparent.
There are no muscles attached to the operculum; but the
flexible portion of the tube below it is retracted by a powerful
muscle, whose fibres are striated, and which is attached below
to the rigid portion of the tube. There is also a muscle by
means of which the alimentary canal is retracted, and to the
base of each tentacle is attached a narrow band of striated
fibre (fig. 2, d), by which, in concert with its fellows, the
tentacular ring is withdrawn, and the action of one or more is
able to draw the crown to one side or the other. There are
also small muscles by means of which the animal is able to
rotate upon its axis. Tor the sake of clearness these muscles
are omitted in the drawing.
In some cases a small projection may be seen upon the side
of the tube near its centre. This is the germ of a future
zooid, so that, in addition to the growth by enlargements
arising in the course of the stolon, each terminal zooid at
least may give origin to another colony, for the zooid thus
developed forms a stolon in the usual way. It should have
been stated, in speaking of the general stolon, that beyond
each zocecium there exists a septum in the course of the stolon,
through which the funiculus runs, having on either side of
the septum a conical enlargement, the bases of the two being
In contact.
The nodal zooids are, as has been stated, generally much
smaller than the terminal and devoid of colour; the tentacles
and stomach are also, as a rule, much less developed. Ana-
tomically, however, there is no difference between them.
The interest attaching to this polyzoon no doubt centres in
406 On the Victorella pavida of Saville Kent.
the fact that we have here a form intimately allied to, if not
identical with, some marine forms, and differing widely from
the freshwater types, but which yet with its host appears to find
itself pertectly at home in fresh water. Mr. Shepherd has,
since seeing my specimens, found it in the Regent’s Canal at
Maida Vale; and I have found it in the Surrey Canal, unac-
companied by any other marine type, or even one found largely
in brackish water, except Plewrosigma.
The small number of tentacles, their setigerous character,
the complete extrusion of the polypide, the absence of epi-
stome, and the striated muscular fibres are distinctly different
from the freshwater type, and are constant characteristics of
the marine type. Much remains to be done before the con-
ditions under which this and similar transfers of marine forms
to freshwater habitats are understood.
It will be seen that my observations differ from Mr. Kent’s
as to the character of the polypidom of Victorella, the presence
of the gizzard, and the nature of the operculum, while, pro-
bably from not using sufficient magnification, he did not
make out the sete upon the tentacles and apparently did not
see the typical form of Véctoredla at all.
In conclusion, I have to acknowledge much kindness
received from Prof. Allman and Mr. Pennington (whose
work on the British Polyzoa is, 1 believe, about to appear).
The latter gentleman relegates Victoredla to the family Cylin-
droeciidee, and has kindly drawn up the following diagnosis :—
Genus VICTORELLA.
Characters as Oylindrecium, but polypides transparent and
having a gizzard. Tentacles eight.
Victorella pavida, S. Kent.
Stem repent, slender, orange-coloured during life, trans-
parent after death; clavate enlargements wide apart. Zocecia
with upper portion erect, cylindrical, transparent, slender.
Below adherent and dilated, forming part of the stolonic
expansions.
Hab. Brackish and fresh water, on Cordylophora lacustris,
whose migrations it follows.
EXPLANATION OF PLATE XIU, Fres. 1-3.
Fig. 1. Portion of stolon at growing end, showing the lateral branches
and young zooids. a, zooid extended; 6, zooid developing ;
c, embryonic zooid at end of branch; d, funiculus,
On the Galatheidea of the ‘Challenger’ Expedition. 407
Fig. 2. Optical longitudinal section through tentacular ring and adja-
cent parts. a, wall of pharynx; 6, thinned margin of same,
reflected to enclose c, circular sinus, which is continued into
g, canal of tentacle ; d, striated retractor muscle of tentacle; e,
perivisceral membrane, reflected over base of tentacle; /f,
operculum.
Fig. 3. A fully-developed but asexual zooid. a, cavity of pharynx; 3,
gizzard ; c, sphincters of gizzard and stomach; d, stomach; e,
intestine ; 7, termination of intestine (7. e. anus); g, termination
of muscular tube attached round anus ; h, tufts of setee crowning
tentacles; 2, funiculus; 4, operculnm.
XXXIX.— Diagnoses of the new Species of Galatheidea col-
lected during the ‘ Challenger’ Haxpedition. By J. R.
HENDERSON, M.B., F.L.S.
[Published by permission of the Lords Commissioners of the Treasury. ]
THE present paper contains brief notices of the new species
of Galatheidea obtained during the cruise of H.M.S. ‘ Chal-
lenger.’ ss some time has elapsed since the return of the expe-
dition in 1876, a number of the species then new to science
have been retaken and described elsewhere. This is espe-
cially the case as regards the group treated of, and four
deep-water genera well represented in the collection, viz.
Galacantha, Hlasmonotus, Diptychus, and Ptychogaster, come
under this category. I am indebted to the courtesy of M.
Alphonse Milne-Edwards for the opportunity of examining
his types from the ‘ Blake’ and the recent French expedi-
tions.
GALATHEA, Fabr.
Galathea pusilla, n. sp.
Rostrum triangular, nearly twice the length of the ocular
peduncles, with a prominent tooth on either side of the base,
and a minute one towards the apex (the latter is occasionally
absent). Carapace smooth and glabrous, the striz not nume-
rous, the lateral borders each with seven or eight spines ;
gastric region with two small spines on either side of the
median line. Chelipedes long and slender, the meral, carpal,
and propodal joints each with three rows of spinules; fingers
parallel and finely toothed. Ambulatory limbs slender and
compressed, with a few spinules especially on the meral
joints.
Length of body (ina g}) 19 millim. ; length of chelipedes
11 millim.
408 -Mr. J. R. Henderson on the new Galatheidea
Loc. Station 163 [off the New South Wales coast], 120
fathoms.
Galathea inconspicua, n. sp.
Rostrum narrow, not twice the length of the ocular pedun-
cles, slightly excavated above towards the base; lateral
borders with four teeth, which diminish in size as they pass
forwards, the central point very long and acute. Carapace
glabrous, the striz fairly numerous and slightly raised ;
gastric region swollen, armed with six small spines, lateral
border eight-spined. Chelipedes and ambulatory limbs want-
ing in the only specimen.
Length of body (in a g) 8 millim.; breadth of carapace
3 millim.
— Loc. Station 194 [off Banda Is.], 860 fathoms.
Munipa, Leach.
Munida spinosa, n. sp.
Rostrum twice the length of the supraocular spines, the
latter nearly twice the length of the ocular peduncles. Cara-
pace considerably narrowed in front, the lateral margins with
seven large spines; gastric region with from six to ten spines
in front, a few spinules on the hepatic and branchial areas.
Chelipedes robust, slightly pubescent, the propodal, carpal, and
meral joints with several rows of large spines. Carpi and
meri of the ambulatory limbs with their anterior borders
spiny. The second abdominal segment with a row of from
six to ten large spines.
Length of body (of adult 3) 56 millim.; length of cheli-
pedes 76 millim.
Loc. Station 145 [off Prince Edward Island], 310 fathoms ;
Station 820 [off the mouth of the Rio de la Plata], 600
fathoms. |
Munida Normant, n. sp.
Rostrum half as long again as the supraocular spines, the
latter about equal in length to the ocular peduncles. Carapace
with two spines on the posterior border, a transverse row of
spines on the cardiac area, and a row of spines on either
branchial region near the borders of the cardiac area, also two
spines on the gastric area; lateral borders of the carapace
with about six spines. Chelipedes cylindrical, covered with
slightly imbricated scales, the inner surface of the joints
(especially of the meri) furnished with spines, the digits long,
of the ‘Challenger’ Expedition. — 409
narrow, and slightly upturned. Meral joints of the ambu-
latory limbs fringed anteriorly by a row of spines and long
hairs. The second, third, and fourth abdominal segments
with four spines each (the two central of which are largest),
the fourth having in addition a single median spine placed
behind the others.
Length of body (of adult 3) 39 millim. ; length of cheli-
pedes 57 millim.
Loc. Station 173 [south of the Fiji Is.], 300 fathoms.
Munida squamoesa, 0. sp.
A species allied to M. Normani, but differmg from it in
the following respects :—The rostrum slender, slightly ex-
ceeding the ocular peduncles, the supraocular spines nearly
the length of the rostrum. Carapace with a mesial spine on
the cardiac region, and one on either side of this near the line
of junction of the branchial and cardiac areas (situated in the
former area). The chelipedes long, slender, and cylindrical,
clothed with imbricated ciliated scales. ‘The ambulatory limbs
also covered with scales, the tarsal joints contorted.
Length of body (of adult g) 52 millim. ; length of cheli-
pedes 81 millim.
Loe, Station 219 [north of the Admiralty Is.], 150 fathoms.
Munida granulata, n. sp.
The surface of this species is everywhere covered by granu-
lations, which in some parts show a tendency to run into
minute spinules or scales ; it is alsoslightly pubescent. Ros-
trum short, in length equalling the ocular peduncles, but
more than double the length of the supraocular spines. The
eyes remarkably compressed. Carapace with a row of small
spines on the posterior border, the cardiac area with three
spines arranged mesially ; gastric region with a central spine
and two placed anteriorly, a few small spines on the posterior
branchial region. Chelipedes long, slender, and cylindrical,
almost naked, the digits long and curved. The ambulatory
limbs also long and slender, with the tarsi contorted. The
second and third abdominal segments with a double row of
spines, the fourth with a single row and raised median protu-
berance behind.
Length of body (of adult ¢) 33 millim. ; length of chelipedes
64 millim. |
Loe. Station 173 [south of the Fiji Is.], 300 fathoms.
Munida scabra, n. sp.
Allied to M. granulata, but differing from it in the following
410 Mr. J. R. Henderson on the new Galatheidea
respects :—The granulations on the chelipedes and ambula-
tory limbs are in M. scabra superseded by small scales, those
on the carapace by minute spinules. he rostrum in this
species is comparatively shorter, and the supraocular spines
separated from one another by a wider interval than in J.
granulata. ‘The arrangement of spines is similar to that in
the last (with the exception that there is only a single one in
the centre of the posterior border of the carapace), but they are
everywhere more strongly developed. Finally, the marking
of the last two abdominal segments is very different in the
two species: in M. granulata it consists of small ciliated
scales, whereas in M. scabra these are represented by raised
concentric lines passing across the segment.
Length of body (of adult ¢) 39 millim.; length of cheli-
pedes 63 millim.
Loc. Station 192 [off the Ki Is.], 129 fathoms.
Munida proxima, n. sp.
This comes nearest to Mf. scabra, but is, however, a smaller
species. ‘The rostrum is shorter, the spinules on the carapace
are more strongly developed, there is no central spine on the
gastric region, and that on the centre of the posterior border
is wanting. ‘The chelipedes are longer and narrower, but
clothed also with minute scales; the digits are long and
straight.
Length of body (of adult 9) 26 millim.; length of cheli-
pedes 44 millim.
Loc. Station 219 [north of the Admiralty Is.], 150 fathoms.
Munida vitiensis, n. sp.
Rostrum nearly twice the length of the supraocular spines,
the latter equalling the ocular peduncles. Carapace furnished
in front with a row of from ten to twelve spines (the two
immediately behind the supraocular spines being larger than
the others), the branchial regions with three small spines;
lateral margins with about seven spines. Chelipedes short
and robust, furnished with hairs and spines, the latter in three
rows. Ambulatory limbs short, the meral, carpal, and pro-
podal joints spiny (the propodi with the spines on the inferior
border). The second abdominal segment with numerous
small spines.
Length of body (of ¢ with ova) 31 millim.; length of
chelipedes 28 millim.
Loc. Station 173 [south of the Fiji Is.], 800 fathoms.
Munida militaris, n. sp.
Allied to 17. miles, A. Milne-Edwards. It is, however, a
of the ‘Challenger’ Expedition. 411
smaller species; the carapace is shorter and narrows poste-
riorly, the gastric region is flatter, and the lateral borders are
furnished with about seven spines. ‘The gastric spinules are
arranged as in M. miles. 'The chelipedes are short and robust,
the principal joints with spines arranged in three rows; the
fingers are in contact throughout. ‘The second abdominal
segment is alone armed with spines.
Length of body (of a ¢) 33 millim.; Jength of chelipedes
28 millim.
Loc. Station 173 [south of the Fiji Is.], 300 fathoms;
Station 192 [off the Ki Is.], 129 fathoms; Amboyna, 100
fathoms. Station 200 [off the Philippines], 255 fathoms.
Munida tnornata, 0. Sp.
Allied to 1. miles and M. constricta, A. M.-E. Rostrum
more than twice the length of the ocular peduncles, the supra-
ocular spines very short (about half the length of the ocular
peduncles) and placed close together. Carapace unarmed, with
the exception of very minute spines on the lateral borders and
arow on the anterior gastric region (of which the two be-
lund the supraocular spines are largest). Chelipedes in the
male long, narrow, and slender, very sparingly armed with
spines, but clothed with imbricated scales. Second abdo-
minal segment with two very minute spines hardly visible to
the naked eye.
Length of body (of a ¢) 26 millim.; length of chelipedes
39 millim.
Loc. Station 219 [off the Admiralty Is.], 150 fathoms.
Munida sancti-pauli, n. sp.
A shallow-water species closely approaching I. miles,
A. M.-H. The carapace is, however, proportionately broader,
the transverse strive are not so strongly marked, and the spines
on the lateral borders are more prominent. Only the second
abdominal segment is furnished with spines.
Length of body (ofa ¢ with ova) 28 millim., length of
chelipedes 29 millim.
Loc. Off St. Paul’s Rocks, 10-60 fathoms.
Munida Haswelli, n. Spe
Rostrum twice the length of the ocular peduncles, the supra-
ocular spines slightly exceeding the latter. Carapace with
the striz numerous, tuberculate, and the hairs densely set;
gastric region with two spines situated behind the supra-
oculars, and several spinules on the hepatic and branchial
areas. Chelipedes slender, the digits long and in contact
412 Mr. J. R. Henderson on the new Galatheidea
throughout. The second abdominal segment with from four
to eight spines.
Length of body (of an adult ¢) 31 millim., the chelipedes
wanting in this the largest specimen.
Loc. Station 163 [off the New South Wales coast], 120
fathoms.
Munida gracilis, n. sp.
A small species resembling the northern M. tenuimana, G.
QO. Sars. The spiny armature of the carapace is similar to
that of the latter, with the exception that there are no spines
on the posterior border. The rostrum is very longand slender,
more than twice the length of the supraocular spines, and
these latter exceed the ocular peduncles. The chelipedes are
of greater length and tenuity than in J. tenuimana, the pro-
podi and digiti being unusually long. The second and third
abdominal segments are alone furnished with spines, and these
are more numerous on the second.
Length of body (of a 9) 24 millim.; length of chelipedes
36 millim.
Loc. Station 166 [off New Zealand], 275 fathoms.
Munida curvirostris, n. sp.
Rostrum more than twice the length of the supraocular
spines, considerably upturned; the supraocular spines as long
as the ocular peduncles, also upturned, but less so than the
rostrum. Hyes very large, with the cornee dilated. Cara-
pace short and broad, the strie not numerous; gastric region
with a row of spines in front, the spines on the lateral borders
very prominent. Chelipedes robust, with several large spines.
Tarsi of ambulatory limbs long. The second abdominal seg-
ment with a row of spines.
Length of body (of a 9) 27 millim.; length of chelipedes
21 millim.
Loc. Station 210 [off the Philippines], 375 fathoms.
Munida spinifrons, n. sp.
Rostrum slender, about three times the length of the ocular
peduncles, the anterior half slightly upturned, and furnished
with a series of well-marked spines on either side; the supra-
ocular spines not equalling the ocular peduncles. Carapace
sparingly clothed with iridescent hairs, gastric area with a
few spines in front, a single small spine on each branchial
area. Chelipedes and ambulatory limbs long and slender.
The second abdominal segment with two small spines.
of the ‘Challenger’ Expedition. 413
Length of body (of ¢ with ova) 19 millim.; length of
chelipedes 22 millim.
Loc. Station 113 a [Fernando Noronha], 7-25 fathoms.
Munida tuberculata, n. sp.
Rostrum about twice the length of the ocular peduncles,
earinated dorsally, and with a slight tendency to serration
near the apex; the supraocular spines short and flattened.
Carapace with the striz well marked and tuberculate, the
gastric region with a row of small compound tubercles in
front. Chelipedes and ambulatory limbs furnished with
tubercles, which show a tendency to become spinulose. The
second abdominal segment armed with a few spines.
Length of body (of a 3) 10 millim.; length of chelipedes
12 millim.
Loc. Station 172 [south of the Fiji Is.], 240 fathoms ; Sta-
tion 173, near the last, 315 fathoms.
Munida spinicordata, n. sp.
Rostrum slightly exceeding the ocular peduncles, the supra-
ocular spines nearly as long as the rostrum, separated by a
wide interval. Eyes large and flattened. Carapace with two
small spines on the gastric region and a prominent mesial one
on the cardiac region, those on the lateral borders very minute,
except the first, which is well marked. Chelipedes very slender,
with a row of spines on the inner border. Ambulatory limbs
long and slender. The second, third, and fourth abdominal
segments with spines.
Length of body (of a ¢) 14 millim. ; length of chelipedes
20 millim.
Loc. Station 174 [off the Fiji Is.], 210 fathoms.
Eumunipa, 8. }. Smith.
Eumunida, Proc. U.S, Nat. Mus. 1883, vol. vi. no. 1, p. 44.
Humunida Smithii, n. sp.
A small species allied to #. picta, Smith. The rostrum and
first pair of supraocular spines deflexed. Lateral borders of
carapace armed with five or six small spines; gastric region
with three minute spinules situated between the second supra-
ocular and the first marginal spine; of these the first is
smallest, whereas in &. picta it is large and prominent.
Chelipedes wanting in the only specimen.
Length of body 15 millim.
Loc. Station 192 [off the Ki Is.], 129 fathoms.
414 Mr. J. R. Henderson on the new Galatheidea
Munipoprsts, Whiteaves.
Munidopsis, Amer. Journ. Sci. 5rd series, vol. vii. p. 212 (1874).
Galathodes, A. Milne-Edwards, Bull. Mus. Comp. Zool. Hary. Coll.
vol. viii. no. 1, p. 53 (1880).
Munidopsis brevimana, n. sp.
Rostrum spinulous, slightly upturned towards the tip.
Carapace glabrous, with small transverse raised lines; gastric
region swollen, armed with two prominent spines, the lateral
borders with four or five spines. Hye-stalks movable, pro-
longed into a delicate spine both above and below the colourless
cornee. Chelipedes shorter than the first pair of ambulatory
limbs, the digits broad and excavated. Ambulatory limbs
having the meral and carpal joints with a row of spines supe-
riorly, the propodi nearly twice the length of the tarsi. The
second, third, and fourth abdominal segments with a slight
transverse bicarination.
It is allied to M4. ( Galathodes) Renoldsi, A. M.-H.
Length of body (of a 2 with ova) 60 millim.; length of
chelipedes 32 millim.
Loc, Station 218 [off the Admiralty Is.], 1070 fathoms.
Munidopsis subsquamosa, n. sp.
Rostrum spinulous and nearly straight, slightly compressed
laterally. Carapace sparingly pubescent, covered posteriorly
with raised imbricated lines (giving a scale-like appearance) ;
in front showing a tendency to become tubercular or spinose ;
gastric region circumscribed, armed with several spines,
the hepatic and anterior branchial regions deeply exca-
vated. Lateral borders of carapace with two prominent
upturned spines in front, and several smaller behind these.
Kye-stalks slightly movable, prolonged into a spine in front
of the cornea. Chelipedes robust, the various joints tubercu-
late, the merus and carpus slightly spiny. Ambulatory limbs
robust, the first pair slightly exceeding the chelipedes, with
the meral, carpal, and propodal joints sparingly tubercnlate
and spiny. Abdominal segments tuberculate, the second,
third, and fourth slightly bicarinate transversely.
Length of body (of a 3) 67 millim.; length of chelipedes
46 millim.
Loc. Station 237 [off the Japanese coast], 1875 fathoms.
Munidopsis Miller?, n. sp.
Rostrum short and spinulous, slightly upturned. Carapace
of the ‘Challenger’ Hapedition. 415
with a few raised transverse lines posteriorly, almost smooth
in front ; gastric region circumscribed, armed with two small
spines (occasionally four) ; the cardiac region circumscribed
and with several spinules on the anterior border. Lateral
borders of carapace four-spined, the posterior border raised,
and armed with from five to eight spines. Chelipedes with
the propodal joints flattened and a single large blunt tooth on
each digit. Ambulatory limbs long and slender. The second
and third abdominal segments transversely bicarinate, the
fourth slightly carinate.
Length of body (of a ¢ with ova) 33 millim.; length of
chelipedes 39 millim.
Loc. Station 207 [off the Philippines], 700 fathoms.
Munidopsis trifida, n. sp.
Rostrum armed with two lateral teeth, the central point long
and upturned. Carapace glabrous, with slight transverse
rugosities; two prominent spines on the gastric region and
four on the lateral borders. The eye-stalks not prolonged
into spines. Chelipedes slender, with three rows of spines on
the meral joints and a single row on the inner surface of the
propodi. Ambulatory limbs long, the meral and carpal joints
with a row of spines on the upper border. Abdominal seg-
ments smooth, the second and third slightly grooved trans-
versely.
It is allied to WZ. (Galathodes) latifrons, A. M.-K., and JM.
(Galathodes) tridens, A. M.-H.
Length of body (of a ¢) 40 millim.; length of chelipedes
47 millim.
Loc. Station 310 [Straits of Magellan], 400 fathoms.
PENG & BEN
Munidopsis pilosa, n. sp.
Rostrum long and spinulous. ‘The body and limbs covered
everywhere with short densely-set hairs. Hyes rudimentary,
the corneze very minute, each ocular peduncle prolonged into
a long spine which runs parallel with but does not equal the
rostrum. Chelipedes very short, not twice the length of the
external maxillipedes. Ambulatory limbs robust, the meral
joints strongly spined above and below.
Length of body (of a g) 24 millim. ; length of chelipedes
10 millim.
Loc. Station 196 [off Gilolo Is.], 825 fathoms.
416 Mr. J. R. Henderson on the new Galatheidea
Evasmonotus, A. Milne-Edwards.
Elasmonotus, A. Milne-Edwards, J. c. p. 60.
Elasmonotus latifrons, n. sp.
Rostrum broadly triangular, simple and flattened. Cara-
pace covered everywhere with rounded tubercles, the regions
well marked. Eyes minute, the cornes rudimentary, ocular
peduncles fused with the side of the rostrum. Chelipedes
robust, granulated. Ambulatory limbs short and robust,
granulated ; upper borders of meral, carpal, and propodal
joints with a row of blunt spines. Second, third, and fourth
abdominal segments transversely bicarinate.
Length of body (of a ¢) 34 millim.; length of chelipedes
23 millim.
Loc. Station 218 [off the Admiralty Islands], 1070 fathoms.
Elasmonotus marginatus, n. sp.
Allied to the last; the rostrum, however, is narrower and
turned up and the tubercles on the carapace larger. The
lateral borders of the carapace are characteristically raised and
project upwards and outwards. The chelipedes and ambu-
latory limbs are clothed with hairs and spines both on the
upper and lower margins, the spines being most prominent
on the carpal and meral joints. The second, third, and fourth
abdominal segments are strongly carinate transversely.
Length of body (of a ? with ova) 50 millim.; length of
chelipedes 32 millim.
Loc. Station 168 [off New Zealand], 1100 fathoms.
Elasmonotus Miersit, n. sp.
Rostrum short, with the sides parallel at first, then abruptly
tapering to the apex. Surface of body and limbs everywhere
minutely granulated. Gastric region of carapace well
mapped out, with two prominent blunt spines in front.
Chelipedes with several rounded tubercles on the inner border
of the meral joints. Ambulatory limbs with a row of tubercles
on both the upper and lower borders of the meral joints:
Abdominal carinz almost obsolete. ;
Length of body (of a 3) 15 millim.; length of chelipedes
17 millim.
Loe. Station 173 [off the Fiji Islands], 300 fathoms.
Elasmonotus asper, n. sp.
In this species the carapace is remarkably flattened and
covered everywhere with rough tubercles, the intervals between
of the ‘Challenger’ EHapedition. 417
these being finely granulated. The rostrum is flattened and
spiniform, with the apex bidentate, the upper point turned up
and blunt, the lower broad and flattened. Chelipedes and
ambulatory limbs tuberculate, the tarsi short and curved, with-
out teeth on the lower border. Second and third abdominal
segments tuberculate, and each with a prominent dorsal
projection.
Length of body (of a ? with ova) 28 millim.; length of
chelipedes 27 millim.
Loc.—Station-107 [off the-eoast-of Brazil], 1500-fathoms-;
station 311 [Straits of Magellan], 245 fathoms.
GALATHOPSIS, n. subgen.
The characters of this proposed new subgenus are some-
what intermediate between those of Munidopsis and Elasmo-
notus. The rostrum is triangular, flattened, and simple,
resembling that of Diptychus. ‘The carapace is swollen and
without spines or ridges, the orbito-antennal border short and
nearly horizontal. The eye-stalks are freely movable and
without spines, the cornee being pigmentless. The limbs
are short and robust. It is distinguished from Munidopsis
by the form of the rostrum and by the absence of spines on
the surface of the carapace; while it differs from Hlasmonotus
chiefly in the form of the carapace, which in the latter genus
is usually depressed.
Galathopsis levigata, n. sp.
Rostrum long and acute. Carapace glabrous, sparingly
clothed with fine hairs; the orbito-antennal border with a
prominent spine behind the eye, also two on the lateral
border near its junction with the former. Chelipedes robust,
clothed with delicate hairs and almost obsolete polished
tubercles ; the digits spoon-shaped. Ambulatory limbs
robust and hairy, with polished scales ; the meral joints pro-
longed into a spine at the upper and outer border, the ‘tarsi
strongly toothed. Internal antenne very short, the basal
joint stout and spiny. Merus of the external maxillipedes
short and broad, with two well-marked spines on the inner
border. Abdominal segments smooth, the second, third, and
fourth faintly carinate.
Length of body (of a 2 with ova) 33 millim.; length of
chelipedes 18 millim.
Loc. Station 219 [off the Admiralty Islands], 150 fathoms.
Galathopsis debilis, n. sp.
Allied to the last, but the carapace is minutely punctate
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 29
418 Mr. J. R. Henderson on the new Galatheidea
and the orbito-antennal and lateral borders are without spines ;
the rostrum also is shorter. ‘The chelipedes and ambulatory
limbs are hairy and minutely granulated. The abdominal
carinee are more strongly marked than in G. levigata.
Length of body (of a g) 18 millim.; length of chelipedes
11 millim.
Loc. Station 173 [off the Fiji Islands], 300 fathoms ;
station 210 [off the Philippines], 375 fathoms.
GALACANTHA, A. Milne-Edwards.
Galacantha, A. Milne-Edwards, /. ¢. p. 52.
Galacantha bellis, n. sp.
Allied to G. rostrata, A. M.-E.*; the granulations of
that species are, however, superseded by small spiniform
tubercles ; the central gastric spine is broader and flatter,
the lateral spines are narrower and separated by a wider
interval, while the spines on the under surface of the base of
the rostrum are smaller, and the latter is more elevated.
Length of body (of a 2 with ova) 65 millim.; length of
chelipedes 38 millim.
Loc. Station 300 [off Juan Fernandez], 1375 fathoms.
Prycuocaster, A. Milne-Edwards.
Ptychogaster, A. Milne-Edwards, Z. ¢. p. 63.
Piychogaster Milne-Edwardst, n. sp. f
Rostrum more than twice the length of the ocular peduncles,
spiniform and upturned. Carapace covered with spines
arranged in longitudinal rows. Chelipedes and ambulatory
limbs very long and slender, covered with rows of spines ;
the digits of the chele smooth and their apposed edges fur-
nished with short hairs and a few minute teeth. All the
abdominal segments thickly beset with small spines.
Length of body (of a ¢) 55 millim. ; length of chelipedes
118 millim.
Loc. Station 310 [Straits of Magellan], 400 fathoms.
Ptychogaster levis, n. sp.
Rostrum slightly exceeding the ocular peduncles, almost
straight. Carapace glabrous, unarmed, with the exception of
a few small spines on the gastric region, the lateral borders
* §. 1. Smith, Bull. Mus. Comp. Zool. vol. x. no. 1, pl. ix.
+ Narrative of the Voyage of the ‘Challenger,’ vol.i. pt. 2. p. 900,
fig. 330.
of the ‘Challenger’ Expedition. 419
with about five delicate spines. Chelipedes very slender,
furnished with rows of spinules, the ambulatory limbs with
spatulate tarsi. Abdominal segments smooth and glabrous.
Length of body (of a 2 with ova) 15 millim.; length of
‘ chelipedes 32 millim.
Loc. Station 192 [off the Kai Islands], 129 fathoms.
Drerycuus, A. Milne-Edwards.
Diptychus, A. Milne-Edwards, J. c. p. 61.
Diptychus insignis, Ni. Sp.
Rostrum long, slightly upturned, with two or three minute
lateral teeth towards the apex. Eyes minute. Carapace
with a row of small spines in front, extending across the
gastric and hepatic regions, the remainder of its surface smooth
and glabrous: the lateral border furnished nearly as far as its
posterior termination with small spines, of which the first and
those corresponding to the ends of the gastro-hepatic row are
largest. Chelipedes robust, the meral and carpal joints
strongly tubereulate and armed with several prominent spines.
Ambulatory limbs with the tarsi short and strongly toothed,
the inferior margin-of the propodal joints produced distally
and furnished with spines.
Length of body (of a $) 32 millim.; length of chelipedes
44 millim.
Loe, Station 145 [off Prince Edward Island], 310 fathoms.
Diptychus spinimarginatus, n. sp.
Rostrum almost straight, long and narrow, the borders with
two or three minute teeth towards the apex. Eyes minute.
Carapace narrowed anteriorly, sparingly clothed with delicate
hairs, especially towards the sides, the posterior half of the
lateral borders armed with five large spines and a few smaller
in front of these. Chelipedes long, slender, and cylindrical,
the carpal and propodal joints smooth and about equal in
length. Ambulatory limbs with the upper border of the
meral joints spiny, the first pair very slender.
It is allied to D. armatus, A. M.-E., but in the latter the
carapace 18 armed laterally with seven or eight spines, and
the ambulatory limbs are smooth.
Length of body (of a 9 with ova) 21 millim.; length of
chelipedes 29 millim.
Loc. Station 170 [off the Kermadec Islands], 520 fathoms ;
station 214 [off the Philippines], 500 fathoms.
29*
420 On the Galatheidea of the ‘Challenger’ Expedition.
Diptychus parvulus, n. sp.
Rostrum about three times the length of the ocular peduncles,
entire, the upper surface slightly hollowed out. Carapace
smooth and glabrous, the lateral borders minutely dentate..
Chelipedes with the meral and carpal joints short and armed
with small teeth, the hand longer and more dilated than either
of the former joints. Ambulatory limbs with the meral joints
slightly dentate, the propodi furnished distally with a series
of spines on the lower border.
Length of body (of a g) 12 millim.; length of chelipedes
17 millim.
Loc. Station 310 [Straits of Magellan], 400 fathoms.
Dintychus politus, n. sp.
Rostrum narrow, only slightly exceeding the ocular pedun-
cles; apex subobtuse. Carapace narrow and glabrous, without
spines or hairs. Chelipedes smovth, the propodal joint
slightly broader and longer than the carpal, the digits with
two rounded tubercles on the inner border, both fingers clothed
at their extremities with delicate hairs. Ambulatory limbs
slender, the tarsal and propodal joints with a few spines,
otherwise smooth.
Length of body (of a g) 15 millim.; length of chelipedes
24 millim.
Loc. Station 171 [north of the Kermadec Islands], 600
fathoms.
Diptychus australis, n. sp.
Allied to the last, but differs in the following respects :—
The gastric region of the carapace is swollen and bears two
very minute denticles. ‘The chelipedes are proportionately
longer and more slender, especially the carpal joints ; the inner
surface of the meral and ischial joints with several rows of
very minute tubercles. The propodi of the ambulatory limbs
long. ‘The squama of the external antenne: equals the ped-
uncle in length, whereas in D. politus it is very small.
Length of body (of an adult ¢) 21 millim.; length of
chelipedes 39 millim. ;
Loc. Station 164 [off Port Jackson], 410 fathoms; station
170 [north of the Kermadec Islands], 520 fathoms ; station
171 [north of the Kermadec Islands], 600 fathoms ; station
194 | off Banda Island], 360 fathoms.
Diptychus gracilimanus, n. sp.
Allied to D. politus and D. australis, but differs from both
Mr. R. Rosenstock on Australian Lepidoptera. 421
in the greatly elongated and slender chelipedes; the eyes also
are smaller than in either of these species. ‘The carapace,
chelipedes, and ambulatory limbs are everywhere smooth and
glabrous.
Length of body (of a @ with ova) 20 millim.; length of
chelipedes 50 millim.
Loe. Station 164 [off Port Jackson], 410 fathoms.
Diptychus tridentatus, n. sp.
Rostrum hollowed out superiorly, the apex tridentate.
Lateral borders of the carapace armed with small spines;
a few minute denticles on the subhepatic region. ‘The
terminal joint of the peduncle of the external antenna pro-
longed into a spine. Chelipedes and ambulatory limbs
wanting in the only specimen.
Length of body (of a ¢ with ova) 12 millim.
Loc. Probably trom the East-Indian archipelago. It is
labelled “‘ Amboyna, 15 fms.,” but, judging from the known
vertical distribution of the genus, this is evidently a mistake.
XL.—Notes on Australian Lepidoptera, with Descriptions of
new Species. By RupDOLPH ROsENSTOCK, B.A.
[Plate XI.]
{Concluded from p, 385. |
Notodontide.
Naprasa, Walk.
(169.) Nadiasa parvigutta, Walk.
Nadiasa parvigutta, Walk. 1. ¢. v. p. 1015.
DIScoPHLEBIA, Feld.
(195.) Discophlebia catocalina, Feld.
Discophlebia catocalina, Feld. Novara Het. pl. xevi. fig. 8.
(419.) Discophlebia Lucasii 9,n. sp. (Pl. XI. fig. 4.)
Head cinereous grey, with a transverse black line in front
of the antenne ; thorax greyish, anterior third tawny brown,
bordered by checolate-brown in front and by a brownish-
422 Mr. R. Rosenstock on Australian Lepidoptera.
black lunular patch behind; a black stripe laterally, covered
by the tegule, and bordered by greyish white behind, crosses
dorsal surface of thorax behind middle; abdomen darkish
grey.
Upperside.—F ore wings purplish grey, with a brownish-
black, basal, #-shaped mark, an irregular dull, faint, greyish-
black band, traversed by a well-defined black, inwardly
whitish-bordered, prominently angulated line; a second dark
reddish-brown undulated ‘line from costa at a short distance
from inner line to about middle of hind margin; orbicular
and reniform spots grey whitish, bordered by dark reddish
brown.
Hind wings dark cinereous grey, with long mouse-grey
hairs upon base and along abdominal margin.
Underside—Fore wings darkish grey, lghter in discal
region ; basal two thirds of costal margin bluish grey, crossed
in middle by an obliquely outwardly-directed, short blackish
dash, forming the dilated upper termination of a subbasal
line, the greater part of which is hidden by greyish hairs
covering the inner discal area of the wing.
Hind wings pale whitish grey, irrorated with bluish grey,
hind margin and apical part of costa broadly bordered by dull
smoky black ; a transverse, smoky black, posteriorly attenu-
ated and abbreviated stripe from costa just before middle;
thorax and basal part of abdomen densely woolly ; fringes
short, greyish, darker at base.
Expanse of wings 43 millim.; length of body 15 millim.
Psychide. ©
THYRIDOPTERYX, Steph.
(837.) Thyridopteryx Herrichii, Westw.
Otketicus Herrichu, Westw. Proc. Zool. Soc. 1854, p. 232, pl. xxxvii.
fig. 3.
CuianiA, Walk.
Clana, Walk. 1. ¢. iv. p. 963.
(369.) Clania tenuis, n.sp. (Pl. XI. fig. 3.)
Allied to Clania Lewinii (Westw. P. Z. 8. 1854, p. 231,
pl. xxxvil. fig. 1), but much smaller and more hyaline. An-
tenn black, head and thorax densely woolly, with inter-
mingled grey and blackish hairs; wings hyaline, covered
with minute, very fine auricular scales; veins brownish.
Expanse 10 millim,
Mr. R. Rosenstock on Australian Lepidoptera. 423
Cymatophoride.
Urasa, Walk.
(266.) Uraba lugens ?, Walk.
Uraba lugens 9, Walk. J. c. xxviii. p. 449 (Phycide).
Cesa viduella $, Walk. U.c. Suppl. v. p. 1729 (Tortrices).
Toxoloma australe 2, Feld. Novara Het. pl. C. fig. 16.
I certainly think the Cymatophoride the right place for
this species. Mr. Meyrick considers it a Pyralid; on what
grounds I utterly fail to see.
NocrvireEs.
Hadenide.
KUPLEXIA, Steph.
(535.) Huplexia confundens, Walk.
Euplexia confundens, Walk. l. c. ii. p. 544.
Leucaniide.
LapuyeMA, Guén.
(593.) Laphygma cycloides, Walk.
Laphygma cycloides, Walk. 1. c. ix. p. 190.
Apparently a species of wide range. All the other speci-
mens in the British Museum, which exhibit no perceptible
difference from that from Australia, are from the Cape.
HADENA, Schrank.
(533.) Hadena bistrigula, Walk.
Hadena listrigula, Walk. Cat. Lep. Het. xi. p. 599.
Homopteride.
Homoptera, Boisd.
Homoptera, sp.
Too much mutilated and worn for description, but very
closely allied to Homoptera (Thermesia, Walk.) tmpropria ¢ ,
Walk. Lep. Het. Suppl. i. p. 1064. The markings exactly
correspond, but. ¢mpropria is much smaller; the male ot the
same species occurs again in the collection under the MS.
designation of Hadena homopteroides, but I cannot find it
under that name in the Catalogue or anywhere else.
424 Mr. R. Rosenstock on Australian Lepidoptera.
Deltoidide.
Ruapsa, Walk.
(324.) Rhapsa suscitatalis, Walk.
Hypena suscitatalis, Walk. 1. c. xvi. p. 83.
Walker did not know the locality of his type.
Bertuta, Walk.
(540.) Bertula thyrisalis, Walk.
Bertula thyrisalis, Walk. l. c. xvi. p. 167.
BLepTiIna, Guén.
(403.) Bleptina? * sordescens,n. sp. (Pl. XI. fig. 11.)
Dull smoky grey. Fore wings with a faintly indicated
transverse median band, having somewhat darker zigzag
inner and outer margins which are irregularly bordered by
clearer greyish white, and containing an obscure ill-defined
pale greyish-white reniform spot, surrounding a linear semi-
lunar greyish dash ; hind margin bordered by a pale greyish-
white border, shghtly iridescent in some positions, and pre-
senting on its inner margin three dentate projections, one
apical, a second more evenly triangular just above middle of
hind margin, and a second bicuspid one near the anal angle.
Hind wings dull smoky greyish, with faint indications of a
median transverse stripe and a pale marginal band as in fore
wings, but with quite straight inner border.
Underside.—Paler, grey whitish, with brownish-grey disco-
cellular spots, small, faint, and indefinite on fore wigs, much
larger, deeper, tinted and subovate on hind wings ; a brownish-
grey transverse stripe, narrow and faint on front wings, broader
and more distinct on hind wings; a broad dull smoky-grey
submarginal band-like effusion, and the pale greyish-white
hind marginal band, with its inner border dentated in fore
wings ; even in hind wings, as on upperside; fringes rather
shorter, greyish white; palpi long, recurved over head and
front of thorax; the first jomt somewhat roughly scaled
* The generic position of this species must be taken as provisional.
Bleptina appears to me to contain a number of species referable to sepa-
rate genera, but which I could not spare time to examine critically. Wena-
tion will be found to be of little help, being, as far as I could see, tolerably
uniform throughout the group, and, in fact, throughout the whole of the
Deltoids. The palpi, wing-form, &c. may afford better aid towards a
rearrangement of the species.
Mr. R. Rosenstock on Australian Lepidoptera. 425
beneath, pale fuscous, with a distinctly raised small darkish-
grey patch of scales just below the point of articulation of the
second joint, which is narrower and smoother than the second ;
third joint shorter, narrower, and smoother, acute at apex,
with a flattened bush of hairs emitted from its inner surface
near the base. Antenne ciliated, one cilium on each side of
each joint being longer and stronger than the rest, greyish
fuscous ; thorax dark purplish grey, with scattered grey-
whitish scales; collar and side tegule well developed ; anal
valves covered by a tuft of silky whitish hairs; abdomen and
legs pale brownish, hind tibize with two pairs of spurs, the
upper pair being much the longer.
Hxpanse 44 millim. ; length of body 19 millim.
The specimen seems somewhat worn, but is, I think, suffi-
ciently well characterized to be identifiable from the description.
LITHILARIA, n. g.
Allied (in shape of wings and specific pattern) to Gisira,
Walk. (Cat. xvi. p. 71), a South American genus, also repre-
sented in Japan.
Palpi very long, ascending and curved backwards over
head; first joint distinctly visible, broad, flattened, and
roughly scaled; second joint long, broad, and flattened,
roughly scaled underneath ; third joint as long as second, also
flattened, but narrower and much smoother, with a loose
bunch of long stiff hairs rising from its base behind ; antenna
ciliated, proboscis long and robust. Head and thorax rather
roughly scaled; abdomen moderately long, slender, with
well-developed anal valves.
Fore wings moderately broad, outer margin slightly fal-
cate from apex to centre, then straight and oblique to anal
angle.
Hind wings somewhat broader, outer margin rounded
slightly undulated.
Venation.—Fore wing: vein 2 from anterior third of cell,
8, 4, 5 from one point at posterior angle of cell; with vein 6
from lower vein 7, the long stalks of veins 8, 9, and vein 10
from the upper angle of a short narrow triangular preecostal
areolet, vein 11 from about half of cell.
Hind wing: vein 2 from a little to the basal side of the
middle of cell, 3, 4, and 5 from same point at posterior angle,
6 and 7 from same point at upper angle, 8 (costal) touching
subcostal only near base.
?
(448.) Luithilaria ossicolor, n. sp.
Pale ochreous whitish (bone-colour) ; the markings, owing
426 Mr. R. Rosenstock on Australian Lepidoptera.
to wear, are very obscure and indefinite, scarcely allowing of
adequate description. They consist of irregular transverse
lines, formed by aggregated darkish-brown scales. There
appears to be on the tore wing a subbasal line from one fourth
of costa to hind margin; a second broader angulated line
from about middle of costa to one third of hind margin, where
it closely approaches the subbasal line; an indistinct, much
blurred discocellular mark, and an irregular submarginal
zigzag line, broadest near its costal end; this and the second
line are continued faintly across hind wing, and here, midway
between them, is another equally faint greyish fuscous line.
There is on both wings a hind marginal series of blackish-
brown interneural dots.
Under surface-—In fore wings strongly irrorated with
blackish grey, and with a brownish costal blotch a little before
apex corresponding to the broad costal end of the submarginal
band on the upperside.
Hind wings much more sparsely irrorated with blackish
grey ; median and submarginal lines more distinct, and inte-
rior subbasal line fainter, except in the middle of the cell,
where it forms a distinct discocellular litura. Hxpanse 29
millim.
PYRALES.
Epipaschiade.
CATAMOLA, Meyr.
Catamola, Meyr. Tr. Ent. Soc. 1884, p. 63.
(509.) Catamola funerea, Walk.
Acrobasis funerea, Walk. 1. c. xxvii. p. 31.
A single large female.
ASTRAPOMETIS, Meyr.
Astrapometis, Meyy. 1. c. p. 67.
(570.) Astrapometis saburalis, Walk.
Pyralis saburalis, Walk, 1. c. xix. p. 914.
Pyralidide.
Messatis, Walk.
(154.) Messatis pyrosalis, Guén.
Endotricha pyrosalis, Guén. Delt. et Pyr. p. 219.
Paconia albifimbrialis, Walk. 1.c, Suppl. iv. p. 125.
Mr. R. Rosenstock on Australian Lepidoptera. 427
Tricomia auroralis, Walk. l. c. p. 1259.
Rhodaria robina, Butler, Ann. & Mag. Nat. Hist. (5) ix. p. 96.
I propose to retain Walker’s first name for the genus of
this much-baptized species, for while recognizing its very
close affinity to Hndotricha, Zell., I cannot follow Mr. Mey-
rick in referring it to the latter genus.
Kurycreon, Led.
(148.) Eurycreon familiaris, Meyr.
Eurycreon familiaris, Meyr. Trans. Ent. Soc. 1884, p. 836.
I have retained Mr. Meyrick’s name, though I am nearly
convinced that he has merely redescribed Walker’s Scopula
segestalis (segestusalis, Walk.), which he must have over-
looked. The type of the latter species is, however, so bad
that it should never have been described.
There is also a fragmentary and unidentifiable specimen of
a species of Paraponyx, St. (47), and a species (170) of
Sedenia, Guén., in a similar condition.
IsopTERYX, Guén.
(219.) Lsopteryx nitidalis ?, Walk.
Isopteryx nitidalis ?, Walk. 7. c. Suppl. iv. p. 1818.
A much worn specimen. Of Walker’s type only a body
and hind wing remain; but there is another more recent
specimen from New Zealand in the collection. I can find no
reference to this species in Mr. Meyrick’s papers.
Scoparta, Haw.
(485.) Scoparia (Scopula) cleodoralis, Walk.
Scoparia (Scopula) cleodoralis, Walk. 1. c. xviii. p. 793.
(99.) Scoparia exhibitalis, Walk.
Scoparia exhibitalis, Walker, 2. c. Suppl. iv. p. 1500.
(748.) Scoparia pusilla, n. sp.
Fore wings dark smoky grey, irrorated with deeper black,
with an outwardly oblique, narrow, transverse, pale greyish-
white band from basal fourth of costa to about basal third of
inner margin; a second irregular, angulated, pale band from
costa at two thirds, and an irregular, abbreviated, angulated,
ill-defined stripe upon hind margin; fringes smoky grey at
base, tips whitish. Hind wings smoky grey, lighter towards
base; fringes as in fore wings.
428 Mr. R. Rosenstock on Australian Lepidoptera.
Underside dull leaden greyish, with faint indications of the
markings. Maxillary and labial palpi blackish, whitish at
tips; antenne minutely blackish and white-ringed. Head,
thorax, and abdomen dull blackish grey. Expanse 11 millim.
In pattern it has some resemblance to S. hawaiensis, Butler,
Hawaian Islands (Ann. & Mag. Nat. Hist. (5) vu. p. 330),
but much smaller, in fact the smallest Scoparia I have seen.
G EOMETRITES.
Urapteride.
IpI0DES, Guén.
(434.) Idiodes siculoides, Walk.
Choara siculoides, Walk. J. c. xxi. p. 291.
Ennomide.
ODONTOPERA, Steph.
(433.) Odontopera australis @,n. sp. (Pl. XI. fig. 9.)
Shining sericeous grey. Fore wings with a slight ochreous
tinge ; a few scattered blackish atoms, and faint grey, some-
what linear irrorations along costal and outer margins; a faint
zigzag subbasal line, a deep black linear discocellular spot,
and a blackish, sharply dentated, submarginal line. Hind
wings paler cinereous grey, without ochreous tinge or markings,
except very faint indications of a discocellular spot and of a
denticulate submarginal line.
Under surface of both wings concolorous, shining grey,
with greyish-brown irrorations, the front wings being some-
what darker and having a pale ochreous-grey speckled costal
border; faintly-indicated discocellular spots and a common
dentate submarginal line, somewhat punctiform on the hind
wings. Head, palpi, antenne, thorax, and abdomen pale
ochreous grey.
Expanse 30 millim.; length of body 8 millim.
Has a good deal of resemblance to Odontopera fragilis,
Butl., from Chili (Tr. Ent. Soc. 1882, p. 356).
(@nochromide.
ArnopiA, Guén.
(688.) Arhodia retractaria, Walk.
Arhodia retractaria, Walk. /. c. xxi. p. 282.
Mr. R. Rosenstock on Australian Lepidoptera.
Boarmide.
BoarMiA, Treitsch.
(679.) Boarmia cognata, Walk.
Boarmia cognata, Wall. 0. e. xxi. p. 892.
TrepHrosia, Boisd.
(834.) Tephrosia fractaria, Guén.
Tephrosia fractaria, Guén. Phal. i. p. 270.
Geometride.
CHLOROCHROMA, Guén.
(657.) Chlorochroma cadmaria, Guén.
Chlorochroma cadmaria, Guén, 1. ec, p. 515,
Topis, Hiib.
(637.) Lodis meandraria, Guén.
Todis meandraria, Guén. 1. c. p. 355.
THALASSODES, Guén.
(102.) Thalassodes, sp.
Specimen too much worn for description.
Acidalide.
Ipm@A, Treits.
(422.) Idea perlata, Walk.
Acidalia perlata, Walk. 1. c, xxiii. p. 776.
(308.) Idea oppilata, Walk.
Acidalia oppilata, Walk. l. e. p. 776.
(408.) Idea albicostata, Walk.
Acidalia albicostata, Walk, 1. c. p. 779.
(495.) Idea repletaria?, Walk.
Acidalia repletaria ?, Walk. 7. c. Suppl. v. p. 1624.
429
(246 and 308.) Worn specimens, unidentifiable and unfit
for description.
430 Mr. R. Rosenstock on Australian Lepidoptera.
(402.) Idea farinalis 2, n. sp.
Palesandy greyish white ; face pale ochreous brown ; palpi
short, not extending beyond head; terminal joint short,
blackish at tip.
Wings dusty grey ochreous whitish, with minute and faint
brownish discocellular spots, and very obscure, hardly distin-
euishable, darker median and submarginal transverse lines,
the former passing outside of discocellular spot on fore wings,
inside of it on hind wings; fringes concolorous with wings.
Underside paler and smoother; no trace of transverse
markings, but discocellular spots distinct, especially on hind
wings. Expanse 26 millim.
Ligiide.
CHLENIAS, Guén.
(596.) Chlenias seminigra 8, nu. sp.
Head, palpi, antennz, and thorax black ; abdomen fuscous-
grey above, blackish below ; legs darkish grey.
Fore wings coal-black on upper, cinereous grey on under
surface ; outer margin obtusely angulated near middle.
Hind wings grey on upper and under sides, with an indi-
stinct, blackish, linear, discocellular spot, only visible on under
surface ; fringes black in fore, greyish in hind wings. Ex-
panse 42 millim.
(258.) Chlenias indecesata, Walk.
Chlenius indecesata, Walk. Lep. Het. xxiv. p. 1153.
Caberide.
STEGANIA.
(644.) Stegania? allongata, Feld.
Stegania ? allongata, Feld. Novara Het., pl. exxxi. fig, 15.
Not a Stegania; its proper family position would appear to
me to be among the Macariide.
Fidoniide.
Fiponta, Treits.
Fidonia perornata, Walk.
Lythria perornata, Walk. Cat. Lep. Het. xxiv. p. 1056,
PANAGRA, Guén.
(302.) Panagra inostentata, Walk.
Panagra inos'entata, Walk, 7. ¢, xxiii. p. 1012.
Mr. R. Rosenstock on Australian Lepidoptera. 431
(672.) Panagra intermiataria, Walk.
Panagra mtermixtaria, Walk. 1, c. xxiii. p. 1000.
(687.) Panagra intercalata, Walk.
Panagra intercalata, Walk. 1. ¢. xxiii. p. 1012.
Dasyouris, Guén.
(311.) Dasyuris metaxanthata, Walk.
Cidaria metaxanthata, Walk. 1. ¢. xxvi. p. 1734,
(478.) Dasyuris decisaria, Walk.
Fidonia decisaria, Walk. 1. c. xxiv. p. 1088.
Larentiide.
Puryssoconus, Butl.
Phryssogonus, Butl. Ann. & Mag. Nat. Hist. (5), ix. p. 94.
(268.) Phryssogonus laticostatus, Walk.
Larentia laticostata, Walk. 7. c. xxiv. p. 1196.
Scotosia canata, Walk. 1. c. xxv. p. 1857 (Butler’s type of Phrysso-
gonus).
LarentiA, Treitsch.
(66.) Larentia solutata, Walk.
Coremia solutata, Walk. J. c. xxv. p. 1319.
CHRYSOLARENTIA, Butl.
(629.) Chrysolarentia vicissata, Zell. MS.
Coremia vicissata, Guén. Phal. ii. p. 421, pl. 9. fig. 5.
(109.) Chrysolarentia lucidulata 3, Walk.
Crdaria lucidulata, Walker, 1. c. xxv. p. 1407.
This species presents all the characters of Butler’s new
genus, to which I have accordingly referred it.
Cassia, Walk.
(617.) Casbia melanops ,n.sp. (Pl. XI. fig. 10.)
Pale greyish brown, with a slight roseate tinge (café au
lait), minutely speckled with dull greyish, especially along
costal margin of fore wings, and with the following markings
common to both wings; a faint, dull brick-red, transverse, some-
what undulated median stripe passing on the fore wings just
outside, on the hind wings inside of a black, orbicular, disco-
cellular spot, which is encireled by a faint fine ring of whitish
432 Mr. R. Rosenstock on Australian Lepidoptera.
scales, largest on the fore wings; a second outer, sharply
dentate, reddish line from 2 length of costa of fore wing to
3 inner margin of hind wings, followed by a submarginal
series of interneural, outwardly deep blackish, inwardly brown-
ish-red punctiform spots, and a hind-marginal series of black
dots upon the ends of the veins. On the fore wings there is
an additional straight, very obscure, reddish, subbasal stripe ;
fringes concolorous with wings.
Underside pale sericeous whitish grey, speckled with black
along costal borders, with discocellular spots as above, but
fainter, and with faint indications, especially on the hind wings,
of the submarginal row of spots.
Head reddish brown. Thorax and abdomen concolorous
with wings.
Expanse 27 millim., length of body 7 millim.
(678.) Another much worn specimen of the same species
with the colour nearly all worn off and markings almost totally
obliterated.
Euboliide.
Eusouta, Dup.
(286.) Hubolia undulata, n. sp.
Head, antenne, and palpi grey, irrorated with brownish ;
thorax sparingly covered with light bluish-white scales. Legs
greyish fuscous.
Fore wings pearly bluish grey, with a series of well-defined,
parallel, narrow, undulated, brownish-grey lines, a short,
black, discocellular spot, and an abbreviated, obliquely in-
wardly directed, blackish, apical dash; a hind marginal
series of narrow blackish dashes, interrupted by clayish brown
ill-defined spots placed upon the ends of the veins.
Hind wings pale grey, whitish towards base, darker greyish
along hind margin, with the dark transverse lines very faint,
distinct only on the abdominal margin, and the clay-brownish
hind marginal spots fainter and much less definite than in the
fore wings; fringes grey-whitish, darker greyish at base.
Underside dark grey, brownish along outer margin, paler
towards base, with undulating lines and cellular spots obscurely
marked.
Expanse 25 millim.
CorEMIA, Gn.
(663 a.) Coremia permissata, Walk.
Coremia permissata, Walk, 1. c. xxv. p. 1817.
Mr. R. Rosenstock on Australian Lepidoptera. 433
(663.) Coremia regulata, Walk.
Coremia regulata, Walk. 1. c. xxv. p. 1318.
(307.) Coremia revulsaria, Walk.
Panagra revulsaria, Walk. 1, c. xxvi. p. 1668.
(105.) Coremia languescens,n. sp. (PI. XI. fig. 8.)
Greyish testaceous brown, with pale greyish-white and dark
blackish-grey undulated and denticulated transverse lines ;
median area forming a deeper, more reddish-brownish band,
angulated on the outside and traversed by blackish undulated
lines, bordered inside and outside by a very narrow undulated
pale whitish line; a narrow, pale whitish, denticulated, sub-
marginal line, rendered obscure by a subapical irregular
cloudy blackish suffusion; between it and the hind margin
is a series of cupreous, reddish-brown, suboval spots, divided
by short black dashes running inward from the black lunular
hind marginal spots; fringes blackish grey at base, tinged
with rosy at apex.
Hind wings ochreous yellow, with abbreviated brownish
and blackish stripes upon abdominal margins, and with a hind
marginal line of blackish connected lunular dashes, as in fore
wings; fringes as in fore wings, but quite pale yellowish
round apex.
Underside pale ochreous, with brownish marginal borders,
followed by a dark fuscous apical suffusion in fore wings,
in hind wings by a broad, irregular, dark fuscous band; base
in both wings powdered with greyish fuscous, median area
with discocellular spots and traversed by several fuscous
undulated lines.
- Head, thorax, and abdomen greyish testaceous brownish.
_ Expanse 28 millim.
Allied to C. mecynata (Camptogramma mecynata, Guén.
Phal. ii. p. 424), but differs in the deeper brownish tint of
fore wings and the absence of a complete blackish hind mar-
ginal border on the upper surface of the fore wings. It must
also bear a very closeresemblanceto Camptogramma bichromata
(Gn. U. c. p. 425), but does not in all respects correspond to
the description of that species.
CIDARIA, Treitsch.
(833.) Cidarta responsata.
Cidaria responsata, Walk. 1. ¢. xxv. p. 1409.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 30
434 Mr. R. Rosenstock on Australian Lepidoptera.
PHIBALAPTERYX, St.
(85.) Phibalapteryx disrupta, Walk.
Boarmia disrupta, Walk. 1. e. xx. p. 391.
(88.) Phibalapteryx phibalapteraria, Guén.
Tephrosia phibalapteraria, Guén. 1. c. i. p. 268.
(490.) Phibalapteryx attributa, Walk.
Boarmia attributa, Walk. @. ¢. xxi. p. 890. ;
A female. A male of this species from Tasmania was
described by Walker as Hemerophila vestita (l.c. xxi. p. 322).
ACODIA, n. g.
A genus allied to Coremia in general body-structure and
form, but differmg by the dentate hind margin of the hind
wings, and more especially by the venation of the fore wings.
Unlike any of the allied genera of the Larentiide (Guén.),
Cidaria, Camptogramma, &c., there is no precostal cell
(aréole); veins 6 and 7 are emitted from nearly the same
point at the upper angle of the cell and run separately to the
hind margin; veins 8, 9, 10, 11 are all branches of a com-
mon stalk, emitted from the subcostal cell 2 of its length
before the upper angle; 8 and 9 forming the forked terminal
branches and rising from a common point; 10 and il given
off separately from the stem. ‘The venation of the hind wing
is normal; veins 6 and 7 rise from a short common stalk, 8
(costal) is united to the cell till just before its anterior angle.
(30.) Acodia pauper, n. sp. (Pl. XI. fig. 7.)
In pattern this species closely resembles Larentia? rufes-
cens, Butler, New Zealand (Cist. Ent. ii. p. 502).
Fore wings pale whity brown, traversed by numerous
parallel undulated brownish lines, with minute blackish dis-
cocellular spots, and with irregular blackish-grey suffusions
upon the costa and within the submarginal border. Hind
wings more whitish towards costa and base, with discocellular
spots and transverse outwardly abbreviated brownish-grey
undulated lines, broadest upon lower part of abdominal mar-
gin; terminal border in both wings formed by a series of
blackish-brown lunular dashes. Fringes darkish grey, with a
narrow, pale whity brown basal line.
Underside pale sandy white; fore wings with costal border
tinged with pale ochreous; a very faintly indicated common
transverse greyish undulated line from 2 costa of fore wings to
Mr. R. Rosenstock on Australian Lepidoptera. 435
middle of abdominal border of hind wings, which have a
second greyish, also ill-defined, submarginal band. Head
pale brownish, irrorated with greyish. Thorax with an ante-
rior transverse blackish stripe and three posterior black spots.
Abdomen pale whitish ochreous, with two distinct black dots
on each segment, and other smaller greyish irrorations.
Expanse 26 millim., length of body 10 millim.
The specimen appears to me somewhat rubbed, and con-
sequently this description may not exactly represent the
appearance of a perfectly fresh insect.
CraMBIDzZ.
Diptychophoride.
DiptycHopuHora, Zell.
(815.) Diptychophora ochracealis, Walk.
Cataclysta ochracealis, Walk. J. c. Suppl. iv. p. 1838.
Diptychophora prematurella, Meyr. Trans. Linn. Sec. N. 8. Wales,
vol. iii. p. 198.
A yery poor example.
Two specimens in the Zeller collection, labelled as Mr.
Meyrick’s species, are absolutely identical with Walker’s
type.
THISANOTIA, Hiib.
(227.) Thisanotia aurantiaca, Meyr.
Thisanotia aurantiaca, Meyr. Proc. Linn. Soc. N. S. Wales, vol. iii.
p. 175, and vol. vii. p. 103.
SOROCOSTIA, n. g.
Antenne of male moderately ciliated; labial palpi fairly
long (about twice the length of the head), porrected, roughly
scaled, third joint quite concealed.
Fore wings with 11 veins, $ and 9 from a stalk rising out
of 7, from about its middle, all into costa, 7 just above apex ;
9 is very short and faint, and without denudation and careful
examination likely to be overlooked.
Hind wings with 7 veins—3 from angle of cell, 4 widely
separated from near middle of cell, 5 and 6 from a stalk, 7
from cell just before middle.
I am obliged to create a new genus of Crambide for the
reception of Hromene ? vetustella, Walker, wrongly placed in
the collection under Diptychophora, and apprently quite over-
looked by Meyrick. In neuration it differs nom any of the
436 Mr. R. Rosenstock on Australian Lepidoptera.
genera described by the latter. Its nearest ally seems to be
Ptochostola, Meyr. (Trans. Linn. Soc. N.S. W. vol. vii.
p- 154).
(489.) Sorocostia vetustella, Walk.
Eromene? vetustella, Walk. 7. c. Suppl. 5, p. 1763.
Head, thorax, and palpi snowy white, sparingly speckled
with fuscous grey. —
Fore wings fuscous grey, with a snowy white, longitudinal,
anculated,costal stripe from base to costa, atthree fifths, container
ing three well-marked blackish spots, one near base, the second
(the largest) at the middle in the angle of the band, the third
smaller at its posterior termination ; the apex suffused with
white, which is continued as a narrow, oblique, white, trans-
verse line to two thirds of inner margin; it is clouded inter-
nally by some irregular darkish suffused markings ; a faint dark
fuscous zigzag subbasal line is continued from below the
second subcostal spot to about one fourth of inner margin.
Hind wings greyish.
I have redescribed this species, as Walker’s type was much
worn, and the description consequently quite inadequate.
ANCYLOLOMIA, Hiibn.
(843.) Ancylolomia ruptella, Walk.
Crambus ruptellus, Walk. 1. c. xxvii. p. 173.
Pnonophora ruptella, Meyr, Trans, Linn, Soc. N.S. W. vol. iii. p. 179,
vol, iv. p. 240.
This species does not belong to the Crambidez, and its
true position is doubtful.
TORTRICITES.
Tortricide.
ACROPOLITIS, Meyr.
(84.) Acropolitis signigerana, Walk.
Tortrix signigerana, Walk. 1. c. xxviii. p. 332.
Sciaphila rudisana, Walk. 1. c. xxviii. p. 849.
Penthina indecretana, Walk. 1. e. xxviii. p. 377.
Acropolitis signigerana, Meyr. Proc. Linn. Soc. N. 8. W. vi. p. 488.
Tortrrix, Linn.
(147.) Tortrix leucaniana, Walk.
Conchylis leucamana, Walk. 1. c. xxviii. p. 370.
Gelechia intactella, Walk. J. c, xxix. p. 652.
Teras pauculana, Walk. 7. c. Suppl. v. p. 1781.
Tortria leucaniana, Meyr. Proc. Linn. Soc. N. 8. W. vi. p. 517.
Absolutely identical with the New Zealand specimens in
Mr. R. Rosenstock on Australian Lepidoptera. 437
the British-Museum collection; forms an exception to Mr.
Meyrick’s statement that no two species are common to the
two countries (/. c. vi. p. 415).
Conchylide.
Bonpia, Newm.
(849.) Bondia nigella, Newm.
Bondia nigella, Newm. Trans. Ent. Soc. Lond. vol. iii. n. s. p. 289; also
Meyrick, Trans, Linn. Soc. N. 8. W, vol. vii. pp. 180-182.
Meyrick’s account of the neuration of the hind wings is not
quite correct, veins 3 and 4 being emitted from the same
point at the posterior angle of the cell, and not remote from
each other.
TINEITES.
Tineide.
Tinga, L.
(792). Tinea comptella, Walk.
Tinea comptella, Walk. 1. c. xxx. p. 1007.
This is certainly not a Tinea, the smooth head, smooth,
flattened, subquadrate face, the narrow, linear, naked, and
widely divergent palpi, combined with the very narrow lan-
ceolate hind wings, lead me to consider it as allied to Butalis.
(842.) Tinea? fraudulens, n. sp. (PI. XI. fig. 12.)
Head loosely haired, deep yellow; palpi dark fuscous;
second joint with a few separate stiff hairs; terminal joint
minutely conical. Antenne nearly if not quite as long as front
wings, dark fuscous. Thorax dark metallic blackish viola-
ceous. Abdomen dark ochreous. Legs dark fuscous.
Fore wings elongate, lanceolate, bright yellow, with a dark
blackish fuscous, oblique, transverse, irregularly bordered
fascia irrorated with dark blue metallic scales from 2 costa to
about middle of inner margin, continued round anal and
apical angles as an attenuated hind marginal border, the whole
forming a D-shaped mark. Fringes greyish fuscous ; under-
side of fore wings and both sides of the rather narrow lanceo-
late hind wings dark golden brownish, with purplish metallic
iridescence ;_ fringes of hind wings dark greyish fuscous,
about 4 breadth of wing.
Expanse 14 millim.
I am doubtful as to the true generic position of this species.
The antenna seem to me too long for a Tinea, though it
438 Mr. R. Rosenstock on Australian Lepidoptera.
agrees with that genus in neuration and characters of palpi.
In pattern and markings, on the other hand, it approaches the
Adelide, and is especially like Hdosa hemichrysella, Walk.,
Java (J. c. Suppl. v. p. 1819), type in B. M.
Adelidz.
ADELA, Latr.
(223.) Adela chrysolamprella, n. sp.
Top of head rather loosely covered with short pale ochreous
hairs; face, basal joints of antennee, under surface of thorax
and of legs sprinkled with golden metallic iridescent scales.
Fore wings purplish violaceous, iridescent, with golden
metallic irrorations, a straight, margined, darkish blue median
band irrorated with coarse blackish, and a few grey-whitish
scales; fringes greyish black, sprinkled with metallic-golden
scales.
Hind wings grey towards base, marginally purplish viola-
ceous iridescent ; fringes greyish black. Hxpanse 54 millim.
The tints of this insect vary with the different position in
which it is held. I am describing it as looked at vertically
from above. 9
Glyphipterigide (Meyr.).
HYPERTROPHA, Meyr.
Hypertropha, Meyy. Trans, Linn. Soc. N.S. W. vi. p. 208.
(701.) Hypertropha divitiosa, Walk.
Anthecia divitiosa, Walk. 1. ec. Suppl. iii. p. 771.
Appears to have been overlooked by Meyrick. Quite di-
stinct from deswmptana, Walk. (Orosana d., 1. c. xxiii. p. 460,
redescribed as thesaurella, Meyr. P. L.S.N.S. W. v. p. 209),
being smaller, the cupreous black marginal border of the
hind wing narrower, and the yellow longitudinal discal band
on the under surface of the fore wing of desumptata being
absent.
Gelechiide (Meyr.).
GELECHIA, Zell.
(807.) Gelechia clerica, n. sp.
Head and thorax glossy white; head smoothly haired;
palpi, second joint dilated with scales in front, blackish below
and at base, white above and at apex ; third joint longer than
second, linear, erected, white; apex blackish. Abdomen
whitish fuscous above, grey blackish beneath. Legs greyish
Mr. R. Rosenstock on Australian Lepidoptera. 439
black. Fore wings narrow, elongated, parallel, margined
with a broad, sharply-defined, deep black, longitudinal, discal
band from base to apex; costa and hind margin bordered
along their whole length by a glossy whitish, longitudinal
fascia. Hind wings pale light greyish, semitransparent.
Under surface of front wings dull leaden grey ; of hind wings
as above.
Eixpanse 15 millim.
Has all the characters of a true Gelechia.
Cryptolechiide (Meyr.).
AGRIOPHARA, n. 2.
This genus presents a remarkable exception in the vena-
tion of the fore wings, veins 7 and 8 being emitted sepa-
rately from the angle of the cell and not from a common
stalk, as is the typical arrangement in all the families into
which Mr. Meyrick bas subdivided the Gelechiide. The other
characters of the genus, and more especially the forking from
a common stalk of veins 6 and 7 of the hind wings, lead me
to refer it to the Cryptolechiide.
Head with appressed scales on face, more loosely scaled
behind and at sides. Antenne stout, strongly ciliated in the
male; basal joint stout, without a pecten; palpi moderate,
bent upward; second joint thickened somewhat roughly
below ; third joint slightly shorter than second, quite smooth,
erect, pointed. Thorax smooth; posterior tibie with long
hairs and four long spines; abdomen rather flattened. Fore
wings elongate, ovate ; apex rounded, hind margin obliquely
rounded, cilia short. Hind wings decidedly broader than fore
wings, emarginate below apex.
Venation.—F ore wing : vein 2 from just before angle of cell,
strongly arched outwards, 3 and 4 from a common moderately
long stalk, emitted at posterior angle of cell; 5 approximated
to the stalk of 3 and 4; 7 and 8 entirely separated through-
out, 7 to apex.
(239.) Agriophara cinerosa, un. sp.
Head, palpi, antenne, thorax, and fore wings ashy grey;
hind wings and upperside of abdomen dull leaden grey ;
under surface of abdomen and legs whitish grey.
Fore wings with a short, longitudinal, outwardly attenuated
and abbreviated stripe from extreme base of costa, and bor-
dered below by whitish scales. Veins, especially the lower
median of the cell and its branches (2, 3, 4), striped irregularly
with dark fuscous.
440 Mr. R. Rosenstock on Australian Lepidoptera.
Underside of both wings glossy lead-grey; front wings
somewhat darker.
Speciesresembles Chimabacche cinderella, Newm. Tr. E.S. L.
new ser. vol. iil. p. 288, pl. xviil. fig. 6 (a species which must
also be referred to this genus, differing utterly from Chima-
bacchide in neuration), but is darker, shorter, and narrower in
the wings, with the dark marking on fore wings forming
distinct stripes instead of spots.
Agriophara diminuta $, n. sp.
Head, palpi, thorax, legs, and abdomen ashy grey. Fore
wing cinerous irrorated with whitish, and with a series of
small linear dark fuscous spots along the margins of wings,
especially distinct on outer margins, and with dark fuscous
irrorations scattered over discal region of wing; fringes
whitish grey, irrorated with blackish.
Hind wings leaden grey, darker along outer margin and
around apex.
Under surface of front wings dark leaden grey; of hind
wines glossy whitish grey.
Expanse 17 millim.
In form and markings similar to cinderella and cinerosa, but
very much smaller.
Conaca, Scott.
Coneca, Scott, Austral. Lepid. pt. 11. p. 26.
(423.) Coneca irrorea 2, Feld. -
Coneca trrorea, Feld. Novara Het. pl. exxxviii. fig. 40.
A damaged and worn specimen; its generic characters
agree perfectly with those of Conwca, and I have little doubt
as to its being the female of Felder’s species, the figure of
which appears to me a poor one.
The affinities of this genus are doubtful. Ihave left it
among the Tineidz, where Felder placed his species. Scott,
followed by Walker, placed it among the Psychide, with which
it has nothing in common, except that the pupa builds a case.
Perhaps it is safest to consider it provisionally as an aberrant
Tineid.
Ccophoride (Meyr.).
PALPARIA, Wing.
(848.) Palparia euryphanella?, Meyr.
Palparia euryphanella?, Meyr. Proc. Linn. Soc. N. 8. W. vii. p. 485.
T believe this to be Mr. Meyrick’s species, though the
Mr. R. Rosenstock on Australian Lepidoptera. 441
single and somewhat worn specimen does not altogether agree
with his description ; but I hesitate to make it a type on a few
small discrepancies which may possibly be due to abrasion.
Hewiocausra (Meyr.).
(12.) Heliocausta limbata, Meyr.
Helhiocausta limbata, Meyr. l. c. vii. p. 471.
(488.) Heliocausta tryphenatella, Walk.
Cryptolechia tryphenatella, Walk. 1. c. xxix. p. 753.
Cryptolechia ecophorella, Walk. l. c. xxix. p. 760; Meyrick, /. c. vii.
Awe us ’ P WEES)
p- ri e
Euuecuria, Meyr.
Eulechria, Meyyr. 1. ¢. vii. p. 508,
(840.) Hulechria leucopsina, n. sp. (Pl. XI. fig. 5.)
Head white; palpi rather long ; second joint passing beyond
base of antennee, white on inner, dark greyish fuscous on
outer surface; third joint dark fuscous ; thorax white, with
small antero-lateral blackish spots; antenne greyish fuscous ;
abdomen wanting, but very probably ochreous as in £&. epi-
causta, to which this species is very closely related. Anterior
legs blackish grey; middle legs yellowish, irrorated with
greyish ; posterior legs glossy pale ochreous opaline whitish,
irrorated with greyish; tibize with long yellow hairs above;
tarsal joints greyish ochreous on inner, darkish grey on onter
surface. Fore wings moderately elongated, apex round, hind
margin oblique, anal angle rounded, pure somewhat irides-
cent white, with an ochreous, almost chestnut- brown trans-
verse fascia, from » of costa to } of inner margin, slightly
dilated near middle; asecond broader, similarly coloured band
enclosing a nearly circular clear white spot from 2 costa to
hind margin, just before anal angle, and an ochreous chestnut,
‘subtriangular, hind-marginal blotch, which nearly touches
the outer margin of the second band near the middle; fringes
pale ochreous whitish, dull slaty grey at apex. Hind wings
glossy grey, with a slight purplish tinge ; tips pale ochreous
irrorated with greyish, and whole of fringe along abdo-
minal margins much paler, whitish ; slaty greyish at apex of
wing. Hxpanse 19 millim.
‘This species is easily distinguished from its nearest allies by
the white spots in the second band and by the basal area being
pure white.
_- In the Godeffroy collection of Microlepidoptera I saw a
specimen noted by Mr. Butler—on Mr. Meyrick’s opinion, I
4492 Mr. R. Rosenstock on Australian Lepidoptera.
understood—as near the genus Hpicausta, resembling it in all
but the before-noted white spot in the second band.
The following species, all belonging to the Cé&copho-
ride *, I am obliged at present to leave under their old
genera, as that portion of Mr. Meyrick’s paper in which they
are treated has not come to hand. With single specimens it
is useless trying to make out their genera from the diagnostic
table, especially as some are characterized from one sex only.
(441.) Ccophora? isabella, Newm.
Ccophora ? isabella, Newm. Trans. Ent. Soc. Lond. iii. (u. s.) p. 295,
pl. xviii. fig. 2.
(131.) Gicophora? subnewella, Walk.
Ccophora ? subneella, Walk. Cat. Lep. Het. xxix. p. 691.
(61.) Cryptolechia? placidella, Walk.
Cryptolechia ? placidella, Walk. 1. c. xxix. p. 751.
(850.) Cicophora? apertella, Walk.
Ccophora ? apertella, Walk. 7. c. xxix. p. 698.
All the other specimens in the collection are from New
Zealand, but they cannot be distinguished from the Australian
form.
HKocuroa, Meyr.
(469.) Hochroa protophaes, Meyr.
Eochroa protophaes, Meyr. Proc. Linn. Soc. N.S. W. vii. p. 457.
One specimen, agreeing very well with Mr. Meyrick’s de-
scription.
PuiLopota, Meyr.
(841.) Philobota fascialis, Fab.
Phalena fascialis, Faby. Syst. Ent. p. 644, n. 128.
Tortrix bimaculana, Don. Ins. New Holl. pl. 40. fig. **.
CEcophora bimaculella, Newm. Trans. Ent. Soc. Lond. iii. (a. s.) p. 298.
Gcophora bimaculana, Walk. J. c. xxix. p. 657; Felder, Novara
Het. pl. exxxviil. fig. 48. ‘ ia
Philobota bimaculana, Meyr. Proc. Linn. Soc. N. 8. W. viii. p. 507.
The Fabrician type of this species is in the Banksian col-
lection.
(25.) Philobota tnterlineatella, Walk.
Ccophora interlineatella, Walk. l. c. xxix. p. 692; Meyzick, J. ¢. viii.
p. 501.
(737.) Philobota pretiosella, Walk.
Psecadia pretiosella, Walk. 1. c. xxviii. p. 538; Meyr. J. ¢. vili. p. 499.
* At p. 877, line 5 from top, for Acophoridee read Gicophoride.
Mr. R. Rosenstock on Australian Lepidoptera. 443
Philobota declivis, Walk.
CEcophora declivisella, Walk, 1. c. xxix. p. 687.
(838.) Philobota athletica, n. sp. (Pl. XI. fig. 13.)
Near Gicophora xanthiella, Walk. (/. c. xxix. p. 693), one
of the smaller and, according to Mr. Meyrick, most ances-
tral species of this large genus, which approaches Hulechria
and Peltophora.
Head deep yellow; palpi whitish yellow above, dark fus-
cous beneath ; antenne, anterior and middle legs dark fuscous;
posterior legs pale ochreous pearly white; thorax reddish
purplish fuscous ; abdomen dark fuscous; posterior segmental
margins and anal tuft pale ochreous pearly white.
Fore wings elongate, rather narrow; costa moderately
arched; apex rather pointed, hind margin strongly oblique,
anal angle moderately rounded ; deep yellow, with a reddish
purple, longitudinal, subcostal, discal, linear dash, widening
and forking out anteriorly into two branches ; the upper con-
tinued along costa to apex, and thence along hind margin
round anal angle, where it unites with the obliquely downward
and forwardly directed lower branch, the whole forming a
suborbicular ring with basally directed angle, giving it some-
what the appearance of a tennis-bat. I ringes pale ochreous
whitish, darker near anal angle.
Hind wings grey; fringes pale ochreous pearly whitish,
with a greyish basal line, yellowish towards apex.
Under surface of both wings shining grey; front wings
somewhat darker, with a brownish tint. HExpanse 17 millim.
Pterophoride.
PLATYPTILUus, Zell.
(751.) Platyptilus emissalis, Walk.
Platyptilus emissalis, Walk. 1. c. xxx. p. 930.
PTEROPHORUS, Geoffr.
(179.) Pterophorus canalis, Walk.
Pterophorus canals, Walk. 7. c. xxx. p. 944,
(16.) Pterophorus
A quite unrecognizable specimen.
?
444 Dr. Henri Blane on Ceratium hirundinella.
XLI.—-Note on Ceratium hirundinella (O. F. Miiller), tts
Variability and Mode of Reproduction. By Dr. HENRI
Buanc*. |
[Plate XIT. figs. 4-9.]
In the ‘Compte Rendu’ of the meeting of the Société
de physique et d’Histoire naturelle de Genéve, on the 17th
April, 1884, p. 545, Prof. Brun cites among the pelagic
vegetation collected in the spring in Lake Leman, near
Geneva, a Cilio-flagellate, Ceratium hirundinella, Bergh,
synonymous with Ceratiwm macroceras, Schr. Without
adding further details, the author of the communication says
that this Peridinian, which is furnished with a strong siliceous
envelope, has occurred pretty abundantly. several times.
Nearly at the same time Dr. Imhof published (Zeitschr.
fiir wiss. Zool. Bd. xl. Heft 1.) the results of his researches
upon the pelagic fauna of the Swiss Lakes, and, among other
new species, described a new Cilio-flagellate which he bap-
tized with the name of Ceratiwm reticulatum.
Knowing the uniformity which exists in the faunas of our
different Swiss lakes, a uniformity which may be so fre-
quently recognized in the numerous investigations made by
Prof. Forel, I tried to discover in the pelagic fauna of the
Lake of Geneva the species of Ceratiwm indicated by Prof.
Brun and the new species described by Dr. Imhof.
In the produce of my very first fishing, performed on a fine
day towards the end of May, I found in abundance, at a depth
of 10 metres, Ceratium hirundinella, O. F. Miillert, and
Ceratium reticulatum, Imhof, in company with another Cilio-
flagellate, which, I think, has not yet been mentioned as
living in our Swiss lakes, namely Glenodinium cinctum, M.
More than this, a considerable amount of material enabled
me to ascertain that Ceratium hirundinella, like the other
species of Ceratiwm so carefully studied by M. Bergh, pre-
sented a great variability of form, and that, in reality, Dr.
Imhof’s new species was not distinct, but rather formed part
of the cycle of this variability.
Before discussing the question of identity between Cera-
tium reticulatum and C. hirundinella, I will give some details
as to the organization of this Cilio-flagellate of the Swiss
%* Translated from the ‘ Bulletin de la Société Vaudoise des Sciences
Naturelles, sér. 2, vol. xx. pp. 805-315, pl. x. (February 1885).
+ To avoid confusion, I always adopt, as the author’s name, that of the
naturalist who first described the animal referred to.
+ Bergh, “ Der Organismus der Cilioflagellaten. Eine phylogenetische
Studie,” Morphol, Jahrb. Bd. vii. Heft 2 (1881).
Dr. Henri Blanc on Ceratium hirundinella. AAD .
lakes, and communicate some new and exact observations
upon the mode of reproduction of this group of microscopic
creatures, which has hitherto been very problematical.
The body of the Ceratiwm of the Lake of Geneva, seen in
front, is flattened, seen from the side nearly biconvex. It is
surrounded and limited by a skeletogenous membrane or
cuirass, which is produced in the shape of horns differing in
dimensions and directions.
One of these horns (fig. 4, a), the largest, is denominated
the anterior horn, the animal always moving in the direction
of this extremity; the three others (fig. 4, 6), or sometimes
only two, of unequal length, are the posterior horns. ‘This
kind of external skeleton is not continuous throughout, and is
not everywhere of the same thickness. About the middle of
the body it becomes excessively delicate and forms a perfectly
well-marked cincture (fig. 4, ce); and the skeleton is also
completely interrupted upon one of the surfaces of the body.
This interruption is formed by a large groove with parallel
margins, nearly perpendicular to the cincture (fig. 4, d) ; it
opens near the base of what I will for the moment call the
great posterior horn, and terminates in a rounded end at the
level of the cincture or a little below it. The width of this
groove, measured in several specimens, varies from 0:014 to
0015 millim., its length is 0-030 millim. It is the surface
of the body which presents this groove that I call the ventral
surface, the other, which has nothing of the kind, being the
dorsal surface.
The skeletogenous membrane is not of a siliceous nature,
as Prof. Brun says, but is formed, as M. Bergh perceived,
of cellulose or of a very similar carbon hydrate ; for in Ceratéa
treated with iodized chloride of zinc, the skeletorenous mem-
brane always became slightly tinged with violet. This
cuirass 18 very transparent, presents no pores, and possesses
a very elegant structure. Under a low power it appears to
be very regularly divided into a quantity of little polygonal
dark areas, separated from each other by small white bands;
under a high power we seem to see that these polygonal areas
are so many little fillets (Ledsten) which, towards the ex-
tremity of the horns, become elongated, and by their super-
position cause the contours of the latter to appear as if slightly
denticulated.
The skeletogenous membrane encloses a protoplasmic mass
which contains a nucleus. The protoplasm, which penetrates
to the extremity of the horns, is differentiated into a very thin
external part, the exoplasm (fig. 5, ex), and a larger internal
part, the endoplasm (tig. 5, en).
446 Dr. Henri Blane on Ceratium hirtndinella.
Treated with osmic acid, chromic acid, or picro-sulphuric
acid, the Ceratia of the Lake of Geneva show an exoplasm
which is not homogeneous, as described by M. Bergh in Cera-
tum and Peridinium; it is rather vacuolar in the species
under consideration (fig. 5, ex). ‘The endoplasm (fig. 5, en),
which is denser, contains very fine granules, large and small
globules of a green or yellow colour, or even red, and, lastly,
other colourless, but very refractive, globules. Of the green
and yellow globules the former are the more numerous ; this
abundance of green globules always gives the living Ceratia
a well-marked greenish coloration, which is produced by
chlorophyll. The quantity of yellow globules varies much
in different specimens; M. Bergh ascribes this coloration to
the presence of diatomine. The red globules are much more
rare than the preceding, and frequently their presence cannot
be recognized ; when they exist there are only one or two of
them. ‘These red globules are very large, always placed near
the ventral orifice (figs. 5 and 6, gl. r.). After the application
of the reagents mentioned above they contract, generally
leaving around them a well-defined vacant space ; each globule
then appears as if contained in a vacuole. M. Bergh, who
observed these red globules in Ceratcum cornutum, regards
them, I believe rightly, as being of an oily nature, and ascribes
to them a part in the act of assimilation. As to the refractive
colourless globules which are observed in all specimens
(fig. 5, gl. g.), they are of a fatty nature, for they are imme-
diately coloured brown by osmic acid.
The nucleus of the Ceratia of the Lake of Geneva is of an
oval form (figs. 5, 6, 2) ; it occupies nearly the middle of the
body, and its longer axis is most frequently parallel to the
~eincture. It is 0-030 millim. long by 0-010 millim. broad ;
it possesses a spherical nucleolus placed excentrically, 0-003
millim. in diameter (fig. 5, nw). The intimate structure of
the nucleus and nucleolus varies according to the histological
reagents employed. In specimens fixed by chromic acid and
stained with picrocarmine, the nucleus appears to be finely
granulated, and the nucleolus like a small homogeneous
refractive body, absorbing more of the colouring substance
than the rest of the nucleus (fig. 5). In other specimens
fixed by picro-sulphuric acid and coloured with acetic car-
mine, the chromatic substance of the nucleus appears in the
form of small bacilli held in suspension in the nuclear liquid
without forming a network of any kind (fig. 5 ds); the
nucleolus, instead of being a well-coloured refractive body,
has precisely the aspect of a vacuole or of a rounded colourless
body (fig. 5 b¢s, nu). The nuclear membrane, which is ex-
cessively thin, 1s always visible.
Dr. Henri Blane on Ceratium hirundinella. 447
M. Bergh* gives no details as to the protoplasm and the
nucleus of Ceratium hirundinella, and contents himself with
saying: ‘‘ As regards the protoplasm, celi-nucleus, &c., this
form appears exactly to resemble Ceratiwm cornutum.” Ac-
cording to this author therefore the nucleus of Ceratium hirun-
dinella is elongated with its longer axis parallel to the longer
axis of the animal, and does not contain any nucleolus. If
these facts were well established I admit that it would require
a great exertion of the imagination to confound under a single
species the Ceratiwm found in the Swiss lakes and the Cera-
tiwm hirundinella of O. F. Miller. But the same author
takes care to add further on, in speaking of the latter form :—
“‘Of this form (in opposition to that above described) I have
observed only a few individuals, and therefore I am unable
to state anything as to its variability; nevertheless the
material was sufficient for me to determine the homologies
and the systematic position of this freshwater form.” It
appears clearly from this phrase that M. Bergh, having a
deficiency of material, has chiefly attended to the external
form of the animal, neglecting to study its protoplasm and
nucleus ; this author, therefore, must not take it ill if I regard
what he says upon this subject as only a simple supposition.
Although I have had under my eye several dozens of
Ceratia I have never been able to discover a contractile
vesicle—an observation which, moreover, is in accordance
with those made by M. Bergh and others.
In describing the skeletogenous membrane I have stated
that it is interrupted on one of the surfaces of the body, the
ventral surface, and that it bounded a large groove; from the
bottom of this groove, when we observe living animals, there
issues a flagellum (fig. 6,7), sometimes as long as the body,
which strikes the water, keeping generally a posterior posi-
tion, while the animal always moves in the direction of the
anterior horn. If the existence of this long flagellum is not
difficult to establish, it is otherwise with the circlet of vibra-
tile cilia, which, according to the authors who have paid
attention to the Cilio-flagellate Infusoria, is placed below one
of the margins of the cincture. I have never been able to
observe any such circlet of cilia in living specimens, or in
others treated with reagents. Nor have I been able to recog-
nize the presence of the two flagella which, according to the
recent observations of Dr. G. KlebsT, replace, in the Ceratéum
* Bergh, loc. cit. p. 216.
+t G. Klebs, “ Ueber die Organisation einiger Flagellaten-Gruppen und
ihre Beziehungen zu Algen unc Infusorien,” in Untersuchungen aus d.
botan. Inst. zu Tubingen, Bd. 1. Heft 2 (Leipzig, 1883).
448 Dr. Henri Blane on Ceratium hirundinella.
cornutum investigated by him, the circlet of cilia described by
his predecessors.
The Ceratium here treated of dies very rapidly ; out of
hundreds captured in the morning I have very often had
difficulty in finding a few specimens in the evening ; most of
them were motionless at the bottom of the vessel; when
examined under the microscope all had the contractile part of
the body issuing through the ventral aperture.
REPRODUCTION.
As yet we are in possession of very few positive facts with
regard to the mode of reproduction of the cuirassed Cilio-
flagellata, and especially of Ceratiwm. ven among these
few facts there are some which have been very differently
interpreted, sometimes as demonstrating a reproduction by
division, sometimes as being stages of conjugation. Thus
Perty * thought he had observed a reproduction by longitu-
dinal scissiparity in a species of Cerat’éwm, which must be the
same as ours; Steinf, on the contrary, that he saw a Cera-
tum of the Baltic reproduce by conjugation. Pouchetf cites
a curious observation made by him upon individuals belong-
ing to the species Ceraiium tripos and furca; he found these
attached to each other, forming chains of three, four, and even
eight individuals—chains which, according to Pouchet, could
not originate from a conjugation. Bergh§ states that he
has several times observed two individuals belonging to the
species Ceratium cornutum united to each other and having no
longer more than a part of their skeleton; he is inclined to
believe in conjugation rather than in division.
That such a contradiction exists in the explanation of the
observed facts is because none of the authors cited has paid
serious attention to the intimate transformations which may
have taken place in the protoplasm and the nucleus. ‘Thanks
to the employment of histological reagents and to numerous
observations made upon living specimens, I can assert that
in all cases Ceratium hirundinella propagates by division,
after a previous division of its nucleus.
I have stated above in describing the nucleus that it was
of an elongate oval form, and possessed only a single
nucleolus; but this is not always the case. Tig. 6 represents
* Perty, ‘Zur Kenntniss kleinster Lebensformen,’ &c. (Berne, 1852).
+ Stein, ‘Der Organismus der Infusionsthiere, III. Der Organismus
der Flagellaten oder Geisselinfusorien,’ i. Halfte (Leipzig, 1878).
¢ Pouchet, “Sur l’évolution des Péridiniens” &c. in ‘ Comptes Ren-
dus,’ tome xcy. p. 794 (1882). See also ‘ Annals,’ ser. 5, vol. x. p. 477.
§ Bergh, loc. cit. pp. 214 and 268.
Dr. Henri Blanc on Ceratium hirundinella. 449
a Ceratium first of all observed in the living state, and which
I succeeded in preserving in Canada balsam, after having
fixed it by means of picro-sulphuric acid and stained it with
picro-carmine. The nucleus of this Ceratiwm is not of the
usual form; it is less elongated, for instead of measuring
0-030 millim. in length by 0°010 millim. in breadth, it is not
more than 0:023 millim. long by 0-013 millim. broad—that
is to say, it has now the form of a regular oval. Moreover,
instead of having a single nucleolus, this nucleus contains
two of them, placed excentrically, at a distance from each
other. Whence do these two nucleoli originate? Is one of
them the nucleolus generally observed in every nucleus,
while the other has been formed independently at the expense
of the chromatic substance ? or are they both the products of
the division of a single nucleolus? Although I have no
observations to prove it, I can nevertheless assume that these
two nucleoli are the products of the division of the single
nucleolus which occurs in every elongated nucleus. In fact
if one of them had been formed at the expense of the chro-
matic substance, the latter would have undergone some
modification in its mode of distribution ; or among the nuclei
examined, which possessed two nucleoli, I must necessarily
have met with at least one possessing one nucleolus smaller
than the other—that is to say, in a condition of growth. I
have never been able to observe either the one or the other
of these two facts; the distribution of the chromatic substance
in the interior of the nucleus was alw ays the same, and the
two nucleoli always possessed the same diameter.
Fig. 7 represents a Ceratiwm of which the nucleus has
undergone a notable transformation as regards its form. It
is neither elongated nor oval, but is strongly constricted in
the middle, and appears to be incompletely divided into two
exactly similar halves, each possessing a nucleolus. The
contents of the nucleus in this specimen are still the same as
in that above described; we remark no peculiar arrangement
of the chromatic substance.
Fig. 3 represents an interesting individual, observed and
drawn in the living state, but which, to my great regret,
could not be preserved in Canada balsam. What strikes one
first of all in this specimen is that its nucleus does not occupy
the usual position; imstead of being situated almost entirely
in the posterior [anterior] region of the body, below the circlet,
it is placed across the latter. As in the preceding individual,
the nucleus still appears as if divided into two equal parts ;
but the central part which unites them is much more slender. -
Important modifications are also to be observed in the
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 31
450 Dr. Henri Blanc on Ceratium hirundinella.
skeletogenous membrane. The ventral aperture is no longer
the same, but is only a very narrow groove; from the base of
the right posterior horn (the Ceratium being seen from its
ventral surface) starts a groove, passing (and this is an
important point to ascertain) exactly over the constricted
portion of the nucleus. This groove traverses the circlet to
reach the left-hand margin of the posterior [anterior] region of
the body, and is continued upon the dorsal surface ; it conse-
quently divides the individual into two dissimilar parts, but
each containing half of the nucleus.
If the reader has carefully followed me in the description
that I have just given of the three individuals drawn in
figs. 6, 7, and 8, he will have no difficulty in recognizing
with me that I have had before me three important stages of
the Ceratiwm under consideration, and that they enable us to
conclude that its reproduction takes place by division.
Thus, to sum up, this reproduction commences by the
division into two equal parts of the original single nucleolus
contained in every nucleus. (According to Prof. Gruber *
the division of the nuclei of Amba proteus also commences
by the division of the nucleoli.) The two halves of the
nucleolus separate from each other and the nucleus acquires
a regular oval form, although its contents do not differ from
what they were before. Then the nucleus becomes con-
stricted in the middle, and this constriction becomes more
and more strongly marked until the nucleus appears to be
formed of two halves united by a sort of bridge of nuclear
substance. At the same time that this constriction becomes
more marked the nucleus changes its position; one of its
halves is situated above and the other below the cincture.
At this period the skeletogenous membrane presents a furrow
which divides it, and causes the Ceratiwm to appear as if
incompletely divided into two. ‘The seissiparity, therefore, is
not truly longitudinal, but still less transverse.
M. Bergh} says that he has frequently had the oppor-
tunity of observing Ceratia, especially Ceratiwum cornutum,
which were deprived of a portion of their skeleton; I have
also had the pleasure of recognizing this same fact in Ceratia
of the Lake of Geneva, and it is one of these specimens that
I have drawn in fig. 9. In this individual the skeletogenous
membrane covered only a part of the anterior region of the
body ; on all the rest of the body it had disappeared, leaving
only the vestiges of a right posterior horn and of a small
* A. Gruber, ‘“ Ueber Kerntheilungsvorginge bei einigen Protozoen,”
in Zeitschy. fir wiss. Zool. Bd. xxxviii.
+ Bergh, doe. cit. p. 214.
Dr. Henri Blanc on Ceratium hirundinella. 451
external horn. The protoplasm thus laid bare had a certain
degree of consistency ; and this individual moved rapidly by
means of its long Hagellum. The above author afterwards
mentions having seen two of these individuals in which a
part of the skeleton was deficient, united or stuck together by
the naked part of their bodies and moving rapidly. M. Bergh
cites these curious individuals without knowing what to
make either of those joined two and two or of those in which
a part of the cuirass is wanting. He does not know.whether
he is to regard the former as being in conjugation or as indi-
viduals in course of division; he rather believes in a conju-
gation; and as to the second sort, he says of them that they
are individuals which have abandoned a part of their cuirass.
These few observations of Bergh’s confirm mine in every
point. This naturalist, when he speaks of individuals united
or joined together, has evidently had under his eyes Ceratia
which were in process of dividing; as to the others, of which
he speaks as individuals which have abandoned their cuirass,
we have only to examine carefully figs. 8 and 9 to be con-
vinced that the Ceratiwm represented in fig. 9 is not an
individual which has, so to speak, undergone an incomplete
moult, but that it is the product of a division. We have only
to remove the right-hand portion of the Ceratiwm in course of
division (fig. 8) to have, pretty nearly, the specimen partly
deprived of its cuirass (fig. 9).
In conclusion, it only remains for me to discuss the question
of identity between the Ceratium of the Lake of Geneva,
which I regard, like M. Brun, as identical with Ceratium
hirundinella, O. F. Miller, and Ceratium reticulatum, the
new species described by Dr. Imhof, and found by him in the
lakes of Zurich, Zug, &ce.
I have said in commencing that the skeletogenous membrane
of the Geneva Ceratium is produced in the form of horns of
different directions and dimensions, namely an anterior one,
the largest, and three, or sometimes two, posterior ones, of
smaller size. When there are three posterior horns, as in the
specimen represented in figs. 6 and 7, the Ceratewm of the
Lake of Geneva has exactly the form of Ceratium hirundi-
nella, O. F. Miill., described and figured by M. Bergh.
When there are only two of them (fig. 5) it resembles Cera-
tium reticulatum, Imhof. But among the specimens with two
and those with three posterior horns I have found others in
which the horn situated outside of the left posterior horn, the
31*
452 Dr. Henri Blanc on Ceratium hirundinella.
animal being seen from the dorsal surface, is no longer a horn,
but only a simple stout spine (fig. 4).
Usually, when this third horn is well developed and quite
evident, the other two posterior horns, which are always
longer than this, diverge more from one another; while if it
is only rudimentary, the two posterior horns are less diver-
gent, and sometimes even nearly parallel. (Compare figs. 4,
6, and 7 with fig. 5.) Dr. Imhof* has found in the Katz-
ensee Ceratia closely resembling his C. reticulatum, and only
differing from it by a small eminence situated outside of the
left posterior horn. This is what he says about it :—‘ Per-
haps this species from the Katzensee might be regarded as an
intermediate form between Ceratium hirundinella, Miller, and
our first form.”
It is to be regretted that M. Imhof had not abundant
material at his disposal, for he would certainly have been able
to convince himself that the Ceratia of the Katzensee were
really an intermediate form. He would have seen that
between the actual well-developed horn and the simple promi-
nence there exist all the passages.
As regards dimensions the Ceratium of the Lake of Geneva
does not differ from those of the lakes of Zurich and Zug, nor
from those found by M. Bergh in the fresh water of the
neighbourhood of Copenhagen. Measured upon several
individuals the distance between the extremity of the anterior
horn and the extremity of the left posterior horn (the indi-
vidual being looked at from the dorsal surface) varied from
0°267 to 0°190 millim. All the specimens observed, whether
with three or two posterior horns, had the same ventral aper-
ture, 0°014-0:015 millim. in width, that is to say, of the same
dimensions that M. Imhof gives for his specimens. I may
remark further, with regard to the buccal aperture, that in
fact the figure given of it by M. Bergh for Ceratium hirundi-
nella is not exactly what M. Imhof and myself have observed;
but I cannot attach any great importance to a simple diver-
gence, which may originate merely from a defect in the
drawing. All the Ceratia of the lake had also the same
cuirass, the description of which given above agrees exactly
with those given by MM. Bergh and Imhof of the cuirasses
of the Ceratia which they had before them. All had the
same protoplasm containing the same nucleus. Nuclei in
course of division occurred in specimens with two posterior
horns and in others with three horns.
This uniformity and constancy in the principal characters
* Inhof, doe. cit. p. 167.
Dr. Wallich on the Rhizopods. 453
authorize me in regarding the Ceratiwm of the Lake of Geneva
as the Cerattum hirundinella, O. F. Miiller, described by
Bergh, and further in seeing in Ceratium reticulatum, Imhot,
only a simple member of the cycle of variability to which this
old species, like so many others, is subject.
EXPLANATION OF PLATE XII. Fies, 4-9.
(All the figures enlarged 300 diameters.)
Fig. 4. Cuirass of a Ceratium hirundinella, seen from its dorsal surface.
a, anterior horn; 0, posterior horns; ¢, cincture; d, ventral
aperture.
Fig. 5. Ceratium hirundinella, seen from its dorsal surface. Only the
outlines of the cuirass are drawn. ez, exoplasm ; en, endoplasm ;
gl.r., ved globules; gl.g., fatty globules; », nucleus; nu,
nucleolus.
Fig. 5 bis. Nucleus of a Ceratiwm hirundinella treated with picro-sulphuric
acid and stained with acetic carmine.
Fig. 6. Ceratinm hirundinella, drawn in the living state and then fixed,
seen from the ventral surface. (f, flagellum.
Fig. 7. Ceratium hirundinella, seen from the dorsal surface.
Fig. 8. Ceratiwum hirundinella, dvawn in the living state, seen from the
ventral surface. s, furrow in the cuirass.
Fig. 9. A Ceratium hirundinella in which a part of the cuirass is deficient,
drawn in the living state and seen from the ventral surface.
pr, naked protoplasm ; ¢, cuirass.
XLIT.— Critical Observations on Prof. Leidy’s “ Freshwater
Bhizopods of North America,” and Classification of the
Rhizopods in general. By Surgeon-Major Watiicu, M.D.
(Continued from p. 384. |
It has been already shown (‘ Annals,’ Nov. 1885) that Prof.
Leidy does not dispute the fact of the animal of “ Quadrula”
being in every respect identical with the animal of Diflugia.
We must therefore not place too implicit credence in the
statement made at p. 143 of his work, that “‘ Quadrula sym-
metrica is the only representative of its genus.” For Prof.
Leidy has yet to explain upon what other basis than the
generic non-identity of an organism with any other known
genus, he considersit legitimate to dissociate Difflugia sym-
metrica from Diffiugia; and, further, how he can recon-
cile the creation of a new genus for the reception of that
form with those ‘ investigations” which (he tells us at
p. 6) ‘rather confirm the view that we can only regard the
more conspicuous and prevailing forms as so many nominal
454 Dr. Wallich on the Rhizopods.
species, in likeness with the species of higher organic forms,
more or less intimately related, and by intermediate forms
or varieties merging into one another.”
Having got rid of every question connected with the cha-
racters of the animal, it is, at all events, satisfactory to feel
that the present inquiry is reduced to the, comparatively
speaking, narrow issue of determining whether the characters
of the test in Quadrula are, or are not, sufficiently unique and
constant to warrant the creation of a new genus for the recep-
tion of Diflugia symmetrica.
As we have already been made acquainted with the cha-
raeters of “ Quadrula” symmetriea as laid down in Prof.
Leidy’s work, let us now turn our attention to the characters
therein given of the genus Diflugia, bearing in recollection,
however, that a genus is little better than an abstract concep-
tion, and that it behoves us to assure ourselves, at every step of
the investigation, that the characters assigned to this particular
genus as a whole, neither exceed nor fall short of the aggregate
characters of the several species included in it. It will be
understood as we proceed why this caution is considered
necessary in dealing not only with the new genus Quadrula,
but with the equally questionable new genus Nebela.
And here let me observe that, owing to the unusual length
and vagueness of many of Prof. Leidy’s definitions and de-
scriptions, however desirable it may be to epitomize them to
the utmost, the end in view would be defeated were any
passages struck out which the author might consider essential
to the due comprehension of the points at issue. When it is
stated that thirty-two pages of letterpress are devoted to the
genus Difiugia as a whole, seven to D. pyriformis, and the re-
maining twenty-five to D. globulosa, D. urceolata, D. cratera,
D.acuminata, D. lobostoma, D.arcula, D. corona, D. constricta,
and, lastly, D. spiralis (of which at least half are, on Prof.
Leidy’s own showing, most variable species), the difficulties
in the way of condensation beyond a certain point will, I
venture to think, become apparent.
The characters given of the genus Diflugia are :—“ Shell
very variable in shape, usually composed of extraneous angular
particles of hyaline quartz-sand, sometimes mingled with other
bodies, such as diatom-cases, sponge-spicules, &c.; the same
forms sometimes composed of chitinoid membrane incorporated
with scattered extraneous particles, or composed in part or
entirely of intrinsic particles of peculiar character. Mouth
inferior, usually terminal....... Pseudopods usually up
to half a dozen or more, cylindrical, simple or branching, com-
monly round at the ends, sometimes spreading and pointed.”
— Op. cit. pp. 95, 96.
Dr. Wallich on the Rhizopods. 455
The characters given of Difflugia pyriformis are :—
“Shell pyriform, flask-shaped or ovoid, with the narrower
pole prolonged into a neck of variable length, of uniform
transverse diameters, or more or less compressed; fundus
obtusely rounded or subacute, or more or less expanded and
variably produced into from one to three conical processes ;
neck gradually and evenly narrowed to the oral end, cylin-
droid, sometimes constricted ; mouth inferior, terminal, circular,
or slightly oval. Structure of the shell usually of angular
particles of quartz-sand, sometimes mingled with diatoms ;
less frequently composed of chitinoid membrane with variable
proportions of diatoms and sand.
“Var. 1. D. pyriformis; the ordinary characteristic form
with the opposite diameters uniform.
“Var. 2. D. compressa ; like the preceding, but more or less
compressed.
“Var. 3. D. nodosa; usually a large form like the latter,
but with the fundus variably produced into from one te
three eminences.
“War. 4. D. cornuta; pyriform, with the fundus provided
with one or two pointed conical processes.
“Var. 5. D. vas; like the ordinary form, but with the
neck defined from the body by a constriction.
“ Difflugia pyriformis is one of the most commen species, and
it presents much variety of shape and size. The shell is
ordinarily flask-like or balloon-form, or, as indicated by the
specific name, pear-shaped, with an oval or ovoid body, more
or less gradually prolonged into a neck, which tapers to the
mouth or is cylindroid, and of variable proportionate length.
-..... Diflugia pyriformis by gradual transition merges
into D. globulosa, D. acuminata, &c.”’—Op. cit. pp. 99 to
105.
For reasons stated at great length by the author (pp. 99 to
105), but which are nevertheless far from being clear, Difiugia
proteiformis is altogether excluded from his list of estab-
lished species. At p. 113 he says:— The name D. protez-
jormis is exceedingly indefinite in its application.” And
further on the characters of D. proteiformzs are again cur-
sorily referred to and followed by the remark that ‘“ Dr.
Wallich uses the name of D. proteiformis in a sort of generic
sense, and regards all other forms of the genus ordinarily
recognized as transitional subspecies and varieties.”
With reference to the last remark I can only say, in all
good faith, “lown the soft impeachment,” and, notwith-
standing the inference it involves, I prefer still to adhere to
my own definitions given below, as being more to the point,
456 Dr. Wallich on the Rhizopods.
somewhat shorter, and, at all events, less hampered by all round
alternatives than those furnished in Prof. Leidy’s work, which
render his definitions practically useless. I therefore request
attention to the subjoined extract from the synoptical list of
the Difflugide, at p. 240 of the ‘ Annals’ for March 1864,
confining myself, however, to those forms only which bear
on the question before us.
“Genus Dirriueia (Leclerc).
“ Characters. Animal a testaceous Amoeban. Pseudopodia
cylindrical or digitate. Test chitinoid, or chitinoid with
additions of mineral matter.
“Species 1. Dijfflugia proteiformis.
“ Characters of Test. Form of embryonic test subspherical,
from ! to } of the diameter in one direction being truncated
and constituting the aperture. Form of mature test extremely
variable.
“ Subspecies 1. Diflugia mitriformis.
“Characters. ‘Test mitre-shaped, more or less inflated at
posterior extremity, and without any fixed ratio between length
and breadth.
“Var. a. D. acuminata. Apex of test acuminate.
“Var. 8. D. spiralis. Anterior third of test bent back upon
its body, so as to present a retort-shape.
“Var. y. D. pyriformis. Shape varying from the pear- to
the balloon-shape.”—Annals, March 1864, p. 240.
Referring to this arrangement Prof. Leidy has drawn
marked attention to my having referred the transitional (or, as
I think they may be more correctly termed, the metamorphic)
series, described and figured in the ‘ Annals’ for March 1864,
to Difflugia pyriformis. he following are my reasons for
having done so.
Taking the characters of “ Quadrula symmetrica” in the
order in which Prof. Leidy records them, we find this organism
described as being ‘‘ remarkable for the construction of its shell,
which is compressed pyriform.” Both of these characters are to
be found in his definitions given above of Difflugia pyriformis,
and also its variety, No. 2, D. compressa. But this is not all.
If we turn to plate xxiv. of Prof. Leidy’s work, which is
devoted to “ Nebela” and “ Quadrula,” we shall see two
tests of Nebela, figs. 11 and 12, which, without looking at the
explanation list, we can at once recognize as constituting an
inseparable bond between Nebela and Quadrula on the
side of incipient mineral metamorphism, and Nebela and D.
pyrtformis on the side of outline. In the explanatory remark
Dr. Wallich on the Rhizopods. | 457
these are described as “ transitional to the compressed variety
of D. pyriformis.” Again, if we turn to pl. xu. of Diflugia
pyriformis, figs. 10,11, 12, and 13, we shall see that these might,
without the least incongruity, have been inserted in pl. xxiv. as
additional, and, in reality, better representations of the meta-
morphism shown in figs. 11 and 12 of that plate. A dozen such
examples might be added to these were it necessary. I must,
however, draw particular attention to the very important fact
that these six figures also agree (as closely as any half-dozen
specimens of the same forms of Difflugide can agree with each
other) with fig. 30, plate xvi., of my series of transitional meta-
morphic forms of Diflugia pyriformis, to which I refer them, as
the first link in the chain of varieties which lead up to Dif
flugia symmetrica. The woodcuts Nos. 3 and 4 at pp. 469, 470
of this paper are in reality specimens of D. pyrdformis, so far as
mere form is concerned ; fig. 3 being the ordinary variety with
the test made up of angular mineral fragments, nearly always
more or less transparent. When the test is covered to this
extent with large and angular mineral particles of varying
sizes and shapes, it has passed the stage at which metamor-
phic action, or, in other words, the combinaton of the siliceous
material impacted into the yielding chitinoid basis of the test,
ean enter into colloidal combination with it. In fig. 2
(at p. 468 of this paper) the metamorphic combination has
gone as far as it generally does in such a form; attention is
drawn to it now chiefly with a view to prove that the pyriform
or mitriform ‘‘ compressed” shape, said to be characteristic
of the shell of Quadrula symmetrica, is one of the typical
characters recorded of Diglugia pyriformis and its variety D.
compressa at p. 99 of Prof. Leidy’s work. Now if we look
at figs. 10, 11, 12, 13 of pl. xi1., representing Difflugia pyri-
formis, and figs. 4 and 12 of pl. xxiv. representing Nebela
collaris, the truth at once bursts on us, that the figures from
pl. xu. of D. pyrtformis might be transferred to pl. xxiv., and
the figs. of Nebela collaris trom pl. xxiv. to pl. xii. of D. pyrt-
jormis, without even an expert in the history of the testaceous
freshwater Rhizopods being able to assert positively that the
whole of the six specimens were anything else than average
specimens of Diflugia pyriformis, I contend therefore that
there is nothing in the shape of the test in Difflugia sym-
metrica to distinguish it from the test of D. pyriformis, or
certain metamorphic forms of Nebela collaris of which I shall
have to speak hereafter in reference to another character.
Figs. 27 to 83 of pl. xvi. appended to my paper in the
‘ Annals’ for March 1864, which Prof. Leidy says I “ de-
scribed as transitional forms of Difflugia symmetrica,” I have
458 Dr. Wallich on the Rhizopods.
already shown have nowhere been so described by me. ‘Those
figures represented forms which were regarded by me in 1864
(and I have certainly not yet seenany reason fornot so regarding
them) as fairly typical varieties around which every heretofore
known published variety of the metamorphic series might
with propriety be grouped. ‘These seven types, with Difflugia
symmetrica, seem to me to cover the whole of Prof. Leidy’s
Nebele, excepting the horned varieties, but only as varieties.
To make species, even in the widest sense, on such a basis
can, I think, hardly be considered in keeping with the spirit
of modern classification as applied to the Protozoa.
The next characters given of Quadrula are :—‘ Shell trans-
parent, colourless, composed of thin* square plates of chitinoid
membrane arranged in transverse or more or less oblique series,
in consecutive or alternating order. ... The general arrange-
ment is like that of tiling with variable regularity... . They
[the plates] are not entirely disposed with the symmetry ex-
pressed by their name, for frequently smaller plates break the
regular succession of larger ones, and sometimes one angle of
a plate replaces that of a contiguousone.”— Op. cit. pp. 142, 143.
I have already ventured to express the opinion that Prof.
Leidy’s views as regards the test of Difflugia symmetrica (or,
as he would prefer to call it, ““Quadrula”’ symmetrica) being
composed of thin square plates of chitinoid membrane ”’ is
erroneous, so far at least as I can speak concerning my own
specimens, which, I may add, have been procured over a toler-
ably wide geographical area. Of course Prof. Leidy’s
specimens may be quite correctly described, inasmuch as the
degree of consolidation attained by every test of the kind in
which there is an admixture of siliceous or any other soluble
mineral substance with the chitinoid basis, must depend on
the quantity of that substance present in the water or mud of
the particular locality in which it was produced. But, for
reasons about to be assigned and which are gleaned from
Prof. Leidy’s own statements, it appears in the highest degree
improbable that the ‘‘square plates” in Quadrula can
be truly described as being ‘‘ composed of chitinoid mem-
brane ’’—if we are to understand the term “ chitinotd” in
the sense in which he applies it to the tests of certain
varieties of Nebela and Hyalosphenia, namely, as being exclu-
sively composed of hardened sarcode altogether unconsoli-
dated by any mineral ingredient which has entered into
colloidal combination with it. Thus Prof. Leidy describes the
test of “Hyalosphenia cuneata,’”’ a member of another very inter-
* The word ‘ thin” was, by a mistake of mine, omitted at p. 882 of the
‘Annals’ for November, line 2 from bottom.
Dr. Wallich on the Rhizopods. 459
esting group of testaceous Amcebans, as consisting “‘ of delicate,
transparent and colourless chitinoid membrane, without trace
of definite structure.” In ‘Hyalosphenia tincta” and “H.
papilio”’ the tests are said to be pale yellow. I have never to
my knowledge fallen in with Hyalosphenia, but am neverthe-
less able to attest the occurrence of equally delicate chitinoid
tests as occurring in one of the commonest forms when
developed under favouring conditions, namely Arcella vul-
garis.
But Prof. Leidy’s view appears improbable for another and
more substantial reason. It is this, that although the plates
of Quadrula are described as above in the letterpress, there
is not in any of the six figures (nos. 20 to 25) of plate xxiv.
of his work, representing different views and forms of the
kind of tests referred to, a single plate that even conveys the
idea of having been intended to represent a true rectangular
figure. On the contrary, with the exception of perhaps five
or six plates out of some two hundred and fifty which nearly
answer to the description of being square, all are more or
less irregular both in their outlines and angles, and in these
respects yield no such evidence of an approach to crystalline
form as is to be seen in some of the other tests represented in
Prof. Leidy’s work as belonging to true Difflugide.
Moreover, nearly all the plates in the figures of Quadrula
(pl. xxiv. figs. 20-25) are drawn as having more or less
convex external surfaces, another character not met with in any
specimens that have fallen under my notice. Indeed, it was
the apparent perfect accuracy of the rectangles and the tabular
surfaces and very definite margins of the plates in my speci-
mens that led me to suspect their being due, in some degree
at least, to crystalline agency, although I was fully alive to
the fact that crystallization under ordinary circumstances is
interfered with instead of being promoted in presence of
colloids.
In Prof. Leidy’s plate x. fig. 26, said to represent a shell of
Diffiugia pyriformis, composed “ of chitinoid membrane tncor-
porated with thin siliceous plates,” some of these are really
rectangular; but I should feel inclined to regard them as
rectangular rods, as their length as compared with their
width in most of the forms exhibiting them varies apparently
from 4 to 1, to10 or 12 tol, or even more; the elongated form in
such examples being in all likelihood the natural consequence
of the siliceous constituent being derived from diatoms, many
of which are of similar proportions. Some plates also, on “a
shell of D. arcula, in pl. xv. fig. 86, and in figs. 16, 17, 18,
and 19 of the same plate, representing D. lobostoma, are in
460 Dr. Wallich on the Rhizopods.
like manner rectangular. Again, in pl. xvi. fig. 22, repre-
senting Difflugta globulosa, we have a test described as being
‘composed of rectangular plates, together with a few * dia-
toms.” This is a most interesting specimen, inasmuch as |
the entire external surface of the test (an oblate spheroid) is
closely studded over with rectangular elongated plates, a
broadly ovate valve of a diatom (apparently a Cocconets) being
faintly visible as adherent to the exterior of the plates, though
so hyaline as not to obscure the plates on the part of the test
covered by it. This form must be regarded not as a tran-
sitional variety between Diflugia symmetrica and those forms
of test made up of an admixture of metamorphic bodies (such
as were stated to be present on the test figured in Prof.
Leidy’s plate x. fig. 26, supra), but as a form which is essen-
tially a second “representative” of the so-called genus
Quadrula, and is actually inserted in a plate devoted exclu-
sively to six forms of Difflugia, viz. globulosa, lobostoma,
arcula, urceolata, cratera, and pyrtformis. To deny this
because the figure of one 1s “‘ pyriform compressed,”, whereas
the other is a compressed spheroid, or because the rectangular
plates in one are true squares, whereas in the others they are
parallelograms, or even because in Difflugia symmetrica there
is a close approach to symmetrical arrangement of the square
plates, whereas in the other the elongated rectangular plates
are not so symmetrically arranged, would be too absurd, when
it is borne in mind that we are discussing the predominating
characteristic so conspicuously manifest throughout the whole
of the vast series of testaceous Rhizopods, namely an infinite
tendency to variation—a tendency which even Prof. Leidy
himself admits while making a new genus out of Difflugia
symmetrica. The only matter for surprise is that so keen an
observer as Prof. Leidy should not, at the first glance, have
detected the intimate connexion just indicated between
“Quadrula”’ and the specimen of Diflugia globulosa to which
T refer. Curiously enough, Prof. Leidy figures, side by side
with this specimen of D. globulosa, a second specimen of the
same form (fig. 21), almost identical in size and quite identical
in figure, in which there are no rectangular plates or disks of
any kind, but the entire test is covered with diatoms as large
as the Cocconeis in fig. 22. The diatoms in fig. 21 are, how-
ever, pointed ellipses, and they are as yet metamorphosed
only to the extent of obliterating their generally very coarse
- striation or cellulation, another significant circumstance in
* Only one diatom-valve is visible on the test in fig. 22. There must
therefore be some inaccuracy in the explanatory note.
Dr. Wallich on the Rhizopods. 461
this case and also in that of the single Coccone?s valve, which,
however, still exhibits the median line and its nodules.
In plate xxii., representing Nebela collaris, figs. 18, 18, 19,
and 20 (the two last “‘ magnified 850 diameters”), are to be
seen perfectly rectangular rods (called “ linear plates” in the
descriptive note), together with oval and round plates of
various sizes, the larger ones exhibiting the curves of oval and
circular diatom-valves. The two highly magnified figures (19
and 20) show the perfect angles of the rectangular plates and
the tabular surface of the ovate and circular ones. But the most
important piece of evidence is furnished by the test (fig. 18),
described as “ shell of narrow rectangular and oval plates, from
which a broad strip was broken away, showing that the fracture
follows the intervals of the plates.” It must be remembered
that the test is a large one, and the fractured aperture extends
diagonally nearly from its apex to its base, not a single plate
appearing to be broken across, but the irregular outline con-
sisting of zigzags, each of which answers pro tanto to a side
or end view of the plates. Hence we may reasonably assume
that the whole of these plates are identical with the plates of
Difflugia symmetrica in being perfectly rigid, strong enough
not to yield to considerable force, and therefore necessarily
composed of a large percentage of siliceous or other mineral
matter in combination with the colloidal basis of the test.
But the nearest approach to the perfectly square figure of
the plates in Diflugia symmetrica occurs in a specimen of
Nebela flabellulum, represented in plate xxii. fig. 19, a broad
balloon-shaped variety, on the front of which there are eight
pertectly-formed “ square plates” scattered regularly among
a crowd of “ circular, oval, and linear plates.’’ In size and
appearance the square plates exactly resemble those of D.
symmetrica, Prof. Leidy (at p. 153) remarks :—‘“‘ Occasion-
ally I have found specimens in which quadrate plates, like
those of Quadrula symmetrica, were mingled with the more
usual structural elements as seen in fig. 19,” ¢. e. in the figure
I have been referring to. Nevertheless, we know Prof. Leidy
has in his definition of “‘Quadrula”’ declared that the test is
“composed of thin square plates of chitinocd membrane,”
apparently forgetful of the following very circumstantial
statement made by him in reference to Nebela collaris, the
very form in which ‘the quadrate plates, like those of Quad-
rula symmetrica,’ occasionally occur.”
‘In breaking the shell,” he observes, “the line of rupture
follows the outlines or intervals of the disks and plates. The
shell [of Nebela collaris| appears to be silicious, as it remains
unchanged when exposed to the action of heated sulphuric and
462 Dr. Wallich on the Rhizopods.
nitric acids” !— Op. cit. p. 151. Indisputable proof being here
afforded by Prof. Leidy of these disks and plates being sili-
ceous, was it wise to assert that those in Difflugia symmetrica
are merely composed of chitinoid membrane ?
It now only remains for me, before passing on from the
question of the generic status of Déflugia symmetrica, based
on the figure and composition of its test, to draw attention to
two or three collateral questions bearing upon what has gone
before. The first relates to a very interesting experiment
made by me with a view to find if rectangular plates resem-
bling those on its test could be produced artificially. The
experiment was eminently successful. It consisted in placing
in a suitable phial finely pulverized organic silica in the form
of “ tabasheer” (a substance well known as a product formed
within the joints of the bamboo) with an alkali and a mixture
of glycerine, gum, the albumen of egg, potassium chlorate,
and, lastly, distilled water, the alkali in solution being kept
apart from the rest of the ingredients by a parchment dia-
phragm, and some cotton wool being placed loosely at the
bottom of the phial for any crystalline or other formation to
form or subside on. The phial and its contents were kept, at
the ordinary atmospheric temperature of summer, in a glazed
bookcase, where they could be examined without being in
anywise disturbed. After about five weeks, to my intense
satisfaction, distinct rectangular (square) plates were visible
with a powerful pocket-lens, having already attained a size
as large as the medium-sized plates usually found in Diflugia
symmetrica, and in every respect resembling them. I would
add that I did not attempt to follow any precise quantitative
formula, but simply went by “ the rule of thumb,” looking
on the first effort as merely tentative and likely to give me
some clue to more accurate measurements on a future occa-
sion. I do not doubt, therefore, that any chemist would be
able to repeat the experiment with perfect success and with-
out the least difficulty. Of course I cannot but regard the
experiment as bearing in a very important degree on the
validity of my hypothesis regarding the colloidal metamorphism
observable in the plates and disks of the more marked forms,
and the chitinous pellets and cylinders observable on the tests
of the less highly metamorphosed forms, such as D. spiralis
and others.
As regards Prof. Leidy’s remark that the plates in D7flu-
gia symmetrica are not so symmetrically arranged as the name
would imply, I have only to state that although I unques-
tionably employed the term to indicate the arrangement of the
plates in regular series, I also applied it to the perfect mathe-
matical figure of the plates themselves.
Dr. Wallich on the Rhizopods. 463
That any real disregard for accuracy was manifest in em-
ploying the specific name symmetrica I deny, for if such hyper-
critical accuracy were indispensable in treating of such organ-
isms as the tests of the Rhizopods, some of Prof. Leidy’s
statements, such, for example, as that about the “ chitinoid
membrane,” would, I fancy, not fail to invoke some rather
more hypercritical. But, apart from this, I maintain that
every one of the specimens I have ever seen indicates all
that is needed to justify the term symmetrica, inasmuch as
tendency towards a definite and symmetrical arrangement is
perfectly clear, the deviation from symmetry being obviously
the result of accident rather than inherent tendency. And
we must not ignore the fact, for it is a fact, that the cases are
almost always exceptional in the organic world in which per-
fect symmetry is observable, the honeycomb being one of the
most familiar examples. But what then? The bee is only
the tool working out a figure which is controlled and directed
by other physical forces and tendencies than those that are
inherent in it. And so it is, I contend, with those “ thin
square plates of chitinoid membrane,” which nevertheless
happen to be silicious and able to withstand heated acids.
The two figures here given of Diflugia symmetrica, though
somewhat roughly drawn,
are nevertheless sufficiently
accurate representations of
the specimens from which
they were taken. In the
larger test it was my desire
to show how accidentally
applied disturbing causes,
whether operating from with-
out, or disturbance caused
by the pseudopodia or chi-
tinosare of the animal, may
occasionally break the regu-
larity of the serial order of
the plates. In no specimen
have I ever seen a truncate angle; and where there has been
any overlapping of plates its character has plainly pointed to
disturbance of some sort acting from without. Both figures,
I venture to think, inculcate this lesson. The three separate
plates convey a fairly correct idea of their symmetrical form.
At p. 151 of his work Prof. Leidy says :—“ Dr. Wallich,
referring to the structure of the transitional forms of Diflugia
symmetrica, which, as previously intimated, I suspect to
464 Dr. Wallich on the Rhizopods.
belong to Nebela collaris, calls the peculiar elements colloid
disks and plates. He remarks that they are derived from
the animal, and not directly from the medium in which it
lives. He supposes, however, that they are formed through
the coalescence of diatoms and other mineral elements with
the chitinoid basal substance of the shell, which then undergo
metamorphosis into all the colloid forms that occur.”
Before proceeding with my observations on the “‘Nebele ”
I must make some comments upon the above statement in
relation to the whole of the series of transitional and meta-
morphic forms referred by me to the genus Difflugia. The
first point on which I lay emphasis is the extraordinary fact
that this short paragraph contains nearly if not quite all
the information Prof. Leidy has vouchsafed to publish concern-
ing the grounds on which the conclusions in question were based.
The second point is one upon which I would lay still greater
emphasis, namely, the fact that, without any explanation what-
ever on Prof. Leidy’s part, the whole of the metamorphic forms
described and figured by me were bodily consigned, as in the
case of Difflugia symmetrica, to a new genus. For, with
exception of the short paragraph above quoted, from the first
page of his work to the last, he has abstained from drawing
attention to my reasons for maintaining that influences in
nature extrinsic as regards the animal, serve in a principal
degree to determine the external structure and constitution of
the ectosare of the naked Rhizopods, and notably the external
structure and constitution of the tests of the testaceous forms.
On the other hand, he has several times gone out of his
way to direct attention to conclusions of mine which he leaves
it to be understood he considers erroneous, but which appear
erroneous only because he has completely misrepresented
them. That this isno exaggeration will be seen on reference
to pp. 150 and 151 of his work, where, in the course of four-
and-twenty lines, he gives the subjoined two versions of the
same inaccurate statement in relation to the Nebele :—
““'The series of specimens represented by Dr. Wallich in
figs. 27 to 33, pl. xvi, vol. xii. Ann. & Mag. Nat. Hist. for
1864, and described as transition forms of Difflugia symme-
trica, appear to me to pertain to the same animal as Nebvela
collaris.”
“ Dr. Wallich, in referring to the structure of the shell of
the transitional forms of Déflugia symmetrica, which, as
previously intimated, I suspect to belong to Nebela collaris,
calls the peculiar elements colloid disks and plates.”
And yet a few pages before, namely at p. 145, he had
already stated in his definition of the genus Nebela, that
Dr. Wallich on the Rhizopods. 465
“in form, constitution, and arrangement ” the sarcode is as in
DiFrFLuaiA, &e.!
Had my facts and conclusions on the subject been contro-
verted, or had sufficient reason been assigned for withholding
them, the matter would have been intelligible. But no such
case has been made out and no such reasons have been fur-
nished. And what has been the result? Why, that during
the last four years the forms specially constituting the subject
of this paper have been mentioned in scientific works and
journals in this country and abroad associated only with Prof.
Leidy’s name, and unaccompanied by any accurate characters
of importance that had not been already assigned to them in
papers published by me fifteen years previously.
In the bibliographical list appended to my name at the end
of the letterpress of Prof. Leidy’s work, the following is the
sole reference to the transitional forms :—
“Transition forms, figs. 27 to 33=NEBELA COLLARIS.”
This line furnishes its own commentary *.
In these circumstances I must be permitted to furnish a
somewhat fuller résumé of the facts upon which the con-
clusions were based which Prof. Leidy summarized as
above, since they directly bear on the status of the Nebele.
I must, however, preface what [ have got to say by men-
tioning that, until very recently, 1 was unaware of the fact
that Prof. Ehrenberg had described and figured an organism
under the name of Difflugia collaris, which must in all pro-
bability have been one of Prof. Leidy’s Nebele, in the ‘ Pro-
ceedings of the Berlin Academy’ for 1848 (p. 218). But
although very imperfectly described by the eminent German
microscopist, no doubt owing to the imperfect lenses then avail-
able, his title to priority of discovery ought to be respected just
as much as in the case of Difflugia symmetrica. Nevertheless
this fact affects Prof. Leidy’s views and mine on these two
genera in very different ways. It adds another powerful reason,
in addition to those already furnished, against the transfer of
the forms included in them to newly created genera; in Prof.
Leidy’s case particularly, since his reference to EKhrenberg’s
* The following errors and omissions in relation to the points under
investigation occur in the text of Prof. Leidy’s work. At p. 142, under
Quadrula, reference is made to “D. proteiformis, var. synumetrica, ‘Annals,’
1868, pl. x.” It ought to be pl. viii.
At p. 145, under Nebela, reference made to D. symmetrica, Wallich,
‘ Annals,’ vol. xiii. 1864, pl. xvi. figs. 27-33. No reference to text given,
and no reference to paper of Dec. 1863, where same form is described.
In the same list appended to Nebela no reference at all is made to the
“ transition forms.”
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 32
466 Dr. Wallich on the Rhizopods.
observations on this organism in the year 1848 show he
was aware of Ehrenberg having discovered and drawn atten-
tion to the form in question (vide Leidy, p. 150). But it also
adds another powerful reason to those I have already adduced
why the transition forms referred by me to Difflugia should be
retained in this genus*. It will be seen that Ehrenberg
described the test as “ pyriform.”
After having stated (‘ Annals,’ May 1864) that no vegetable
or extrinsically derived substances are, in my experience,
employed for the consolidation of the Difflugian tests, I
alluded to the selective faculty of the animals as being so
remarkable that colourless mineral particles, sometimes quart-
zose, sometimes felspathic, sometimes micaceous, seem to be
always chosen, as one or other of those minerals happens to be
present in the mud of the locality inhabited by them, and that
the particles are impacted into the chitinoid matrix in so
workmanlike a manner as to leave only the smallest intervals
between adjoining masses and as little overlapping as possible.
Reference was next made to the fact that the testaceous forms
when living in streamlets, where they incur a risk of being
swept away, reduce this risk to a minimum by loading their
tests with as large particles of mineral matter as they can
utilize. It was also stated that the mineral particles used
are not always of inorganic origin, diatoms of various kinds
being promiscuously employed in some tests, whereas in
others a selection has been made of one kind only out of the
various forms present in the same habitat. And, finally, I re-
marked on the metamorphic forms of Difflugide, belonging for
the most part to the mitriform and pyriform series, in which
the chitinoid matrix of the tests presents no appreciable
admixture with unmetamorphosed mineral matter, but is more
or less closely covered over with composite bodies of various
forms andsizes. The whole of the forms now referred to were
minutely described as they present themselves to us in the
metamorphic series, of which figures are given in the plate
attached to my paper above referred to.
My reasons were then expressed for arriving at the con-
clusion that, except in the case of a few permanent varieties
which present a type capable of being hereditarily trans-
mitted, the whole of the varieties of Difflugian tests may be
regarded as the result, first, of modifications in figure,
dependent sometimes on the inability of the test to sustain its
* Ehrenbere’s definition of D. collaris is as follows:—“ D. collars,
n. sp. D. lorica sub ostio in colli formam attenuata, pyriformi, subcla-
vata recta, superficie irregulariter cedlwlosa (!), cellulis parvis eequalibus,
colli angustioribus, apertura integra” (Monatsb. 1848, p. 218).
Dr. Wallich on the Rhizopods. 467
own weight, and sometimes on the tendency to curvature or
obliquity from the pressure of running water; secondly, of
modifications in the materials of which the tests are constructed,
sometimes depending on the kind of mineral substances pro-
curable in particular localities, sometimes on a hitherto unre-
cognized and remarkable union between the chitinoid basal
substance (which is an exudation from the animal) and the
mineral particles, which that substance serves in the first
instance merely to cement together; thirdly, of modifications
in size, depending probably on the age, the perfect or imper-
fect nutrition of the animal, and also on the capability of the
test to alter its form after having become consolidated to a
certain extent by addition of mineral matter; fourthly, and
lastly, of modifications in colour, arising partly from the
nature of the food taken by the animal, partly from the
external incrustation of organic or inorganic débris, and
partly from the tint acquired by the chitinoid basal substance.
I next went on to state that the true nature of the rectan-
gular plates of Difflugia symmetrica would become manifest
as I proceeded with the description of the transitional forms
that intervene between the most aberrant which is repre-
sented by that form, and the least aberrant form, viz. Difiugia
pyriformis and its immediate varieties, which are represented
by such very partially metamorphosed forms as are depicted
in figs. 30 and 31 of the plate accompanying my paper. As
already stated, in none of my papers on the subject of these
Difflugide have the metamorphic series been described as
transitional forms of D. symmetrica, as alleged by Prof. Leidy.
On the contrary, in the explanatory notes annexed to pl. xvi.
‘Annals,’ March 1864, fig. 26 is thus described :—“D. sym-
metrica, showing the rectangular hyaline plates: a, form of
aperture ; b, a more compressed specimen, in which the aper-
ture (e) is nearly closed; d, a few detached plates.
““ Figs. 27 to 33 represent the series of forms exhibiting the
transition from the ordinary mineral and chitinoid elements
of the test to the evolution of the colloid disks.”
And, lastly, in the explanatory remarks appended to pl. viii.
of my paper in the ‘ Annals’ for Dec. 1863, the following is
the description given of fig. 16, pl. viil., p. 467 :—“ Test of
Diffiugia pyriformis, var. symmetrica (Wall.), showing sym-
metrical arrangement of the crystalline plates.”
As some of the readers of the ‘ Annals’ may not have
access to the volumes for 1863 and 1864, in which typical
figures of all the most remarkable Difflugian forms were
given, I have been enabled through the courtesy of the editors
to insert a few figures in illustration of special emacs to
32
468 Dr. Wallich on the Rhizopods.
which I wish to draw attention in connexion with the forms
to which reference has been made in the present and last
month’s instalment of this paper. The first figure in my list
represents in outline one of the simplest and most common
forms of Difflugian test, namely the mitriform—simplest
because it approaches most closely to the spherical form (which
there is reason to regard as the archetype of the entire
Difflugian series) and constitutes also the earliest stage of
most of the varieties of Difflugian tests which in the adult stage
bear scarcely any resemblance to it: the tendency to variation
in outline being, according to my view, neither resident in the
animal nor in the test, but in the varying external conditions,
which give the first impetus to change of figure when the
young test has not as yet lost its purely membranous
character, and is therefore still perfectly plastic. Once set
in motion, the same external forces or influences (for some
are really forces, whereas others are merely influences)
continuing to act in the same direction naturaily tend to
stereotype and extend the characters first impressed on the
young test. It is in this way, I contend, that whereas we
have but one type of animal to deal with, we have an
almost infinite vartety of tests. It follows, therefore, that if
we attempt to do more than group together the various —
most closely related varietal forms and kinds of test on some
definite system based on a knowledge of the forces or in-
fluences which observation teaches us are the most effec-
tive agents in the results produced, we are simply the victims
of an old-world illusion that may serve to amuse, but cannot
instruct, those who indulge in it.
The annexed figure (fig. 2) must, for present purposes,
be Jooked at without reference
to the rectangular plates seen
imbedded at its centre. As
a matter of fact, this par-
ticular sketch was made to
illustrate a point in connex-
ion with Diffugia symmetrica,
of which mention will be made
presently. Apart, therefore,
from the presence of those
plates and a slight deviation
from the original outline, which
is by no means uncommon,
the figure might represent a
varietal form either of D. miéri-
formis or of D. pyriformis.
Dr. Wallich on the Rhizopods. 469
If we now take fig. 2 of D. mitriformis as we find it, with
its admixture of rectangular plates, we shall recognize in the
presence of the latter and the barely perceptible undulation at
the margin of the mouth of the test, distinct evidence of meta-
morphism from the ordinary to the transitional type, of which
(as has before been stated) Diffugia symmetrica is the most
pronounced and aberrant variety. But I would particularly
mention that, even as the figure stands, it was not selected to
illustrate the earliest and most frequent aspect of metamor-
phism, of which a representation was given in fig. 30 of the
series included in the ‘ Annals’ plate of 1864, showing the
whole of the small quartzose particles or minute diatom-valves
plainly melting, as it were, into the substance of the chitinoid
and colloid basis of the stratum on which they rest. The occur-
rence of these siliceous plates in the midst of insoluble mineral
particles proves that they originate only in mineral substances
capable of entering into colloidal combination with the chiti-
noid basis of the test. Hence they furnish clear evidence
that there exists no intrinsic tendency in Difflugia symmetrica
towards the development of these plates, which is not shared
equally by the other varieties of the series. This, I venture
to think, is confirmed by the specimens figured in Prof.
Leidy’s work to which attention has already been drawn in
this paper.
Fig. 3 is a representation of the common form of Difflugia
pyriformis, in which the massiveness of
the angular mineral particles is such as Fig. 3.
to render them apparently proof against §
metamorphic agency. Itwill be seen
on reference to the two figures of
Difflugia symmetrica at p. 463, that
they both partake of the pyriform
curve, though never to a very marked
extent—this being my reason for de-
scribing the figure of the test in D.
symmetrica aS corresponding most
closely with D. mitriformis.
The two next sketches (figs. 4 and 5)
represent very perfect specimens of
highly-developed metamorphic forms,
almost identical in every respect with
those represented in figs. 82 and 33 of ™
my ‘Annals’ series. Fig. 4 shows the test covered with
round colloidal disks of nearly uniform size, placed in more or
less regular order, but invariably resting upon their flat sur-
470 Dr. Wallich on the Rhizopods.
faces, the entire intervals being Fig. 4.
studded with much more minute
disks or globules (for it is almost
impossible to determine positively
which they are). We have in this
and also in fig. 5 typical exam-
ples of the pyriform test of
Diffugia pyriformis, the only
difference between them consist-
ing in the degree of inflation in
the body. of the test—a differ-
ence which is shown to extend
still further in pls. xxii. and xxiii.
of “Nebela collaris” in Prof.
Leidy’s work. In fig. 5 (a
Greenland form) very minute
specimens of a diatom, probably an Hunotia, take the place of
some of the colloid disks. It is,
however, inthe series oftests which
are chiefly built up of diatoms that
a clue is found to the formation
of the large and small colloid
disks, and rectangular siliceous
plates derived from this source.
In some tests the process of meta-
morphism can be very distinctly
traced, and we then see in differ-
ent specimens and _ different
varieties a gradual passage from
their original figure to one or
other of the various metamorphic
forms of which mention has been
made. Where large oval or cir-
cular diatom-valves have formed
part of the test these appear, in some of Prof. Leidy’s figures,
to pass eventually into true circular or oval hyaline plates of
proportionately large dimensions. ‘
I have only space to add that the appearances described as
characterizing the metamorphic series are not confined to the
mitriform and pyriform varieties, though they would appear to
reach their climax in them. They are likewise observable
in the globular and oblique, or, as | have termed it, the mar-
supiiform series, of which Difiugia spiralis and D. cassis
are offshoots. In the former of these two the chitinous pellets
and cylinders, whether straight or bent, seem to arrive at their
maximum of development. But, strange tosay, I have never
Dr. Wallich on the Rhizopods. 471
met with a single example anywhere in which there occurred
so close an approach to distinct siliceous rods and plates as
is to be seen in pl. xix. of Prof. Leidy’s series. I have
nevertheless met with specimens of D. cassis in which there
was a row of circular colloid disks surrounding the aperture of
the test.
Before bringing my remarks on the Difflugian Rhizopods
to a close, I must point out that, although Prof. Leidy has
paid me the compliment of adopting nearly every fact and
conclusion of mine in relation to the forms he has transferred
to his new genus Nebela, the only direct reference made by
him to my previous writings on these forms is contained in
the following brief paragraph at p. 151 of his observations on
the Nebelide; and even here the scope of the remark he is
quoting is very materially impaired by his having cut short
the sentence at the word “ occur’ :—
“Dr. Wallich, in referring to the shell of the transitional
forms of Difilugia symmetrica, calls the peculiar elements
colloid disks and plates. He remarks of them that they are
derived from the animal and not directly from the medium in
which it lives. He supposes, however, that they are formed
through the coalescence of diatoms and other mineral elements
with the chitinoid basal substance of the shell, which then
undergo metamorphosis into all the colloid forms that occur.
Of this process I have been unable to satisfy myself; but the
exceedingly varied specimens which have come under my
notice, of shells composed of elements apparently intrinsic and
of regular but widely different forms, of others apparently of
extrinsic elements, regular and irregular, with many others
of a transitional character, would appear to justify the con-
clusion of Dr. Wallich.”—Op. cit. p. 151.
The sentence quoted from p. 234 of the ‘Annals’ for
March 1864 concludes as follows :—“ from the first alteration
in shape of the mineral particles themselves, to the development
of the crystalline tablets which were first described.”
The genus Nebela is thus defined by Prof. Leidy :—
“¢ Shell usually compressed pyriform, transparent, colourless,
with or without appendages, composed of cancellated mem-
brane, or of peculiar intrinsic structural elements of variable
form and size, mostly of circular or oval disks, of narrow rec-
tangular plates or rods, or of thin, less regular, angular plates,
often almost exclusively of one or the other, sometimes of two
or more intermingled in variable proportions, sometimes of
chitinoid membrane incorporated with more or less extrinsic
elements, and sometimes of these entirely, as in Diflugia.
472 Dr. Wallich on the Rhizopods.
Mouth inferior, terminal, oval. Sarcode colourless, in form,
constitution, and arrangement as in Difflugia, Hyalosphenia,
&ce.”.— Op. cit. p. 145.
“In composition the shell [of Nebela collars] is of extraor-
dinary character, from the variety in form and arrangement of
its elements. Most frequently it is composed of oval or
circular disks. The disks usually hold no relationship in size
with that of the shell; . . . . sometimes the shell is almost
entirely composed of circular disks, sometimes of oval disks,
and frequently the two kinds are intermingled. Sometimes
they are of pretty uniform size; at others, they are intermin-
gled, of different sizes. Most frequently the larger disks
occupy the fundus and body and the smaller ones the lower
part or neck of the shell. Sometimes the larger disks are
more or less scattered, with some approach to uniformity, and
the intervals are occupied by smaller ones. Indeed, there
exists almost any conceivable arrangement of the round and
oval disks in the construction of the shell.”—Op. ev#. p. 147.
“‘ Not unfrequently there are found, in association with the
usual more characteristic varieties of N. collaris, individuals
which have the same form of shell, but with tts structure
rather related with that of the ordinary forms of Difflugia. In
some specimens the shell is composed of thin and wregu-
larly angular silicious plates as represented in fig. 12.”—
Op. cit. p. 148.
“Sometimes narrow rectangular plates in different propor-
tions are intermingled with the disks, and occasionally the
former greatly predominate. Occasionally I have found speci-
mens in which guadrate plates, like those of Quadrula sym-
metriea, were mingled with the more usual structural elements.”
— Op. cit. p. 153.
“The specimens vary greatly in the form of the com-
ponent silicious plates, which consist of variable proportions
of the kind just described, with others which are more regularly
rectangular, or in the form of rods, and sometimes with diatoms
and round or oval plates, like those which ordinarily com-
pose the shell of Nebela collaris. Through such specimens the
latter would appear by transition forms to merge into Diftlugia
compressa !’’-—Op. cit, p. 148.
“The nature of the singularly varied shell of Nebela col-
laris I have not been able to determine with any satisfaction.
In the characteristic forms, the elements of structure, the disks
and plates, appear to be intrinsic, and not of a foreign character.
They appear to be cemented together or conjoined at the
borders, and not implanted upon or incorporated with a distinet
chitinoid membrane. In breaking the shell the line of frac-
Mr. G. A. Boulenger on new Species of Geckos. 473
ture follows the outline or intervals of the disks and plates.
The shell appears to be silicious and remains unchanged when
exposed to the action of heated sulphuric and nitric acids.” —
Op. cit. p. 151.
The encystation of the naked and testaceous Amcebans,
the process of “coagulation” and ‘‘consolidation”’ of the
ectosare by which the membranous structure of the en-
cysting sac is produced, the formation of the diaphragm
by which the mouth of the testaceous Ameebans is closed
during their encystation, and the characters each of these
parts assume, will be found described by me in the ‘ Annals’
for May 1863, pp. 367 to 369; ‘ Annals,’ Nov. 1863,
p. 336; ‘ Annals,’ Dec. 1863, p. 462; and ‘ Annals,’ March
1864, p. 235.
It only remains for me to say that more admirably and
truthfully executed figures of the freshwater Rhizopods
have never been issued than those contained in Prof.
Leidy’s work. Inno other publication have such indisputable
proofs ever been brought together of the process of natural
evolution from one end to the other of a very extensive and
complete series of Protozoan organisms. Had Prof. Leidy
dwelt somewhat more fully and distinctly than he has done
on this the most striking feature in his researches he would
indeed have conferred benefits of no ordinary magnitude upon
the branch of science of which he is so distinguished an
expositor®.
XLUI.— Descriptions of three new Species of Geckos.
By G. A. BouLENGER.
Gecko pumilus, sp. n.
In habit similar to Lepidodactylus Guppyit. Head small,
body elongate, limbs moderate. Snout once and one third
the diameter of the orbit, which equals the distance between
the latter and the very small, round ear-opening ; forehead
scarcely concave. Head covered with small granules, which
are considerably larger on the snout; rostral quadrangular,
not quite twice as broad as long, with a short cleft above;
nostril pierced between the rostral, the first labial, and three
nasals; twelve upper and ten lower labials; three or four
* I have but recently seen Mr. Romyn Hitchcock’s “Synopsis” of
Prof. Leidy’s great work, and can confidently recommend it as a most
useful compendium of information on the freshwater Rhizopods in general,
474. Mr. G. A. Boulenger on new Species of Geckos.
transverse rows of small hexagonal chin-shields. Dorsal
scales uniform, minutely granular; ventrals much larger,
roundish-hexagonal, subimbricate. Digits one third webbed,
strongly dilated, with ten or eleven angularly curved lamelle
under the median toes. A short angular series of eleven
preanal pores (merely indicated, the specimen being a female).
Tail cylindrical, slightly depressed, covered with uniform
small flat scales, largest inferiorly. Pale reddish brown above,
brownish white inferiorly ; a dark line on the loreal region ;
a few small black spots on the tail.
millim
Motallemot hn. way. scrern chor picks cies stele 84
lead ammsrceent stones ce acd even rene 10
Wadthrotiheada seit. ertertatet chute 55
INOINE bod GooAdo no oUt OGOUOOR dd O 30
Roredimibyernd aa ee ee ote 10
JE Fa lIbU ST ems era Meme crm ceo arate ovo 14
Day Ulery cress coe aigateeauaut Mak seks aoe at ance eee 44
A single female specimen, from Murray Island, collected
by the Rev. 8. Macfarlane.
This species is so closely allied to those of the genus
Lepidodactylus that the propriety of separating it from the
latter appears to me somewhat doubtful. However, by its
undivided infradigital lamelle it agrees with the genus Gecko,
as at present defined.
Homopholis macrolepis, sp. n.
Head oviform, depressed, its depth contained twice in its
length ; snout as long as the distance between the eye and
the ear, scarcely longer than the diameter of the orbit ; fore-
head and interorbital space concave; ear-opening small,
roundish-subtriangular. Head covered with small granules,
which are considerably larger on the snout; rostral six-sided,
twice as broad as long, its three upper sides in contact with
the anterior nasal and an internasal ; nostril pierced between
the rostral and six scales, the two anterior of which are the
largest ; eleven or twelve upper and eleven lower labials ;
none of the lower labials deeper than broad; mental small,
trapezoid ; a row of small chin-shields, the two median in
contact with the mental. Dorsal scales larger than ventrals ;
about eighty-five scales round the middle of the body. Limbs
as in H. Wahlbergii. Tail with imbricate scales as on the
body, on the upper surface much smaller than on the lower.
Uniform greyish above.
Prof. F. J. Bell on Lumbrici with bifid Hinder Ends. 475
millim
Motalilong tlt. ciaeteys ae sistercpepscars el 170
TAGS see aver aly sysenhs acta nates nee eek 26
Wradthwot head@cmas cee ecco 20
SOG y stp ict eta cea rane seco shee 69
i orenlimibyar eee. coctre ce o ey eee 30
JabhavsM boat )ne 8G eee aiming een Hees Oe 42
ARE eRe ccc ie esr Ree OT OG ORE cea i)
A single female specimen, from Delagoa Bay; presented by
the South-African Museum, Cape Town.
Phoptropus ocellatus, sp. n.
Head much depressed; snout broadly rounded, a little
longer than the diameter of the orbit, as long as the distance
between the latter and the ear; latter rather large, elliptical,
oblique; forehead not concave. Head covered with flat
granules, largest on the snout; rostral trapezoid, separating
the nasals ; nostril pierced between the first labial and two
nasals ; latter not swollen; seven upper and six lower labials ;
mental large, subtriangular, broader than long, in contact with
two chin-shields ; the chin-shields graduating into the smaller
gular scales. Dorsal scales small, granular; ventrals much
larger, roundish-hexagonal, imbricate. Limbs shorter than
in £. afer; the adpressed hind limb reaches the axilla. Inner
digit very short, not half the length of second. An uninter-
rupted series of thirty-one femoral and preanal pores in the
male. Grey above, with round, dark-edged, whitish spots ;
a rather indistinct dark line on each side of the head, passing
through the eye ; lower surfaces whitish.
millim
Brom snout to yvent...+..1...5..esanee 30
18 LEY 0 late hea Rat ech enema Re eke Seal uA 11
Wradth of neadhinen re ees Jaen re lk W
Moreplinab syed os as hd ee ee seals 14
aS Bravo Mbsan] jue eee he Pieenia ar an Gene 18
A single male specimen, from Cape Town; presented by
the South-African Museum.
XLIV.—Notice of two Lumbrici with bifid Hinder Ends.
By Prof. F. Jerrrey Bex, M.A.
On the 20th of June last Dr. Giinther received from Dr. Kirk-
man, of Hastings, a small earthworm (Lumbricus terrestris)
which was remarkable for having the hinder third of its
body bifurcated. The figures now given are reproductions of
the sketches made a few days later by Mr. Mintern; they
476 Prof. F. J. Bell on Lumbrici with bifid Hinder Ends.
exhibit the natural size of the worm, and the form it took
when moving at ease. It will be observed that the left
branch appears to be a little shorter than the right; and at
times this difference appeared to be better marked, so that
an observer would frequently remark that the left branch
looked like a bud. That it was not so was proved by this
one fact, that, as time went on, the difference in size became
more marked.
For more than two months the worm was under my care,
and I sedulously attended and watched it.
On August 21 it was still very lively, and for the first time
there were apparent some indications of a future clitellum, of
which as yet there had been no sign; but even these were
still obscure. There was now a very definite difference be-
tween the left- and the right-hand branches, the former being
not only smaller but much less active.
On the 25th of August Mr. Hesse (the taxidermist to the
Zoological Department, to whose charge I committed the worm
during an absence from London) observed that the creature
had lost its “ tails,’ and on the 29th of August it was found
dead.
On the 22nd of August Mr. Harting was kind enough to
hand to me an example of a“ brandling” (Lumbricus fetidus)
which had been forwarded to him by Mr. Robert Service, of
Miss 8S. G. Foulke on Trachelius ovum. 477
Maxwelltown, Dumfries, on account of “ its bifurcated tail ;”
this specimen was dead, and was unfortunately sent dry.
The only specimen known to me which presents a similar
arrangement of the hinder end of the body is in the Anato-
mical Department of the University Museum at Oxford, a
short notice of which was published by Mr. Charles Robert-
son in 1867*.
The specimen having died after losing its ‘ tails,”’ and the
portions having been lost during my absence from London,
there has been no opportunity of making an anatomical inves-
tigation; had I done so I should, I am sure, have found the
dorsal blood-vessel dividing into equal branches at the point
of bifurcation, and I should, I think, have found the enteric
tract in the right half a little larger than that in the left.
My primary object in this notice is to put on record an
occurrence which, it is possible, is not very rare, but which
has, at least, escaped general observation. It can be but
matter of guesswork what was the nature of the accident
that preceded the appearance of the bifurcated end; it is
almost as hard to see exactly what the phenomenon does
teach us :—
1. It makes it quite certain that, like lizards with their
tails, earthworms may reproduce bilaterally what is ordinarily
only produced terminally. But this is only another way of
saying that earthworms are subject to a well-known and
widely diffused “ law.”
2. The fact that the clitellum only became apparent a few
days before the loss of the hinder end is positive; but the
events may or may not have any relation to one another. If
they have, they only show that when the earthworm is repro-
ducing parts of its body it is, pro tanto, comparable to a form
reproducing itself asexually, a phenomenon which, so high
in the scale of organization, is, we know, not compatible or
contemporaneous with sexual reproduction.
XLV.—Trachelius ovum. By Sara GWENDOLEN FouLKet.
In first describing this Infusorian, Ehrenberg attributed to it
the possession of a much ramified cesophageal canal ; but his
view, subsequently upheld by Claparéde and Lachmann, has
been strongly opposed by W. Saville Kent, who claims that the
so-called alimentary canal is merely the granular protoplasm
* Quarterly Journal Microse. Sci. vii. (1867), p. 157. I am indebted
to Mr. Robertson for this reference.
+ From the ‘ Journal of the New York Microscopical Society.’
478 Miss 8S. G. Foulke on Trachelius ovum.
highly vacuolate. My own observations had coincided with
those of Mr. Kent, and recently strong confirmation of his
opinion was obtained from the following phenomena :—
I had taken from a Chara-bog numbers of Tracheliz.
Their unusually large size—one fortieth of an inch—afforded
special advantages for observation. In colour the specimens
were a transparent creamy yellow. When first removed to
the live-box they uniformly showed the ventral side to be
flattened and deeply indented longitudinally, so that a trans-
verse section would be kidney-shaped. After a confinement
of some minutes they became globose in contour, and thus
they remained during captivity; but when they were set free
the indentation soon reappeared. In one specimen the granular
reticulation, at first finely shown, seemed to become less pro-
fusely ramified, and a current of the protoplasm towards the
central mass was noticed. This flow continued until all the
smaller branches were massed at a subcentral point, leaving
the rest of the body apparently hollow. One pseudopodium-
like process was now sent to a more posterior point in the
periphery, and the flow was resumed, this time outwards,
until the protoplasm was collected into a nodule attached to
the cell-wall, along which a small portion flowed, afterwards
remaining motionless. No nucleus could be detected in this
specimen, though present in all others examined.
The above condition remained unchanged for nearly an
hour, when, wishing to test the apparent hollowness of the
cell, I removed from the live-box all but a small portion of
the water, and pressed the Trachelius with a blunt knife-blade.
Complete collapse ensued, and the animal now resembled a
twisted rag.
It seemed, however, nowise injured by the operation, as,
after about six hours passed at the edge of the water, it
resumed its globose shape, and free motion about the live-box
again began.
An accident prevented further investigation, but, from the
diffused condition of the nucleus, incipient reproductive phe-
nomena were suspected.
In this connexion I should like to draw attention to a form
described by me in a communication to the Academy of
Natural Sciences of Philadelphia, March 4th, 1884, under
the name of Trachelius Letdyi. ‘The distinction then made
with regard to shape having been rendered invalid by the
observations above noted, colour and the more profuse vacuo-
lation of the periphery alone remain, and, regarding these as
insufficient differences, I have decided to withdraw the species.
Mr. E. P. Ramsay on the Egg of Echidna hystrix. 479
XLVI.—Description of the Marsupial Egg of Echidna
hystrix. By Epwarp P. Ramsay, Esq., F.L.8., C.M.Z.S.
To the Editors of the Annals and Magazine of Natural History.
GENTLEMEN ,—
Since the publication in the Ann. & Mag. Nat. Hist.
No. 84, December 1884, of the “ Description of an Impreg-
nated Uterus and of the: Uterine Ova of Echidna hystrix,”
I have been favoured with a letter, dated ‘ Australian
Museum, Sydney, September 14th, 1885,” from my valued
correspondent Edward P. Ramsay, Hsq., F.L.S., Curator of
that museum, with the following result of his researches on
the same physiological subject.
Sheen Lodge, Richmond Park. RICHARD OWEN.
“To-day [I presume the date of his letter] I got another
fine female Echidna: I now have four. On examining her
pouch I found therein an egg, white in colour and about half
an inch in length, having a rather tough skin, with, I fancy,
very little lime in it, and very like that of a reptile. It is
oval, equally rounded at either end. The beast showed great
resentment at being examined, and, being a very prickly
subject, I had not much time to examine the egg, as I was
afraid of breaking it. The pouch was much warmer than the
body of KEchidnas generally. I was much surprised at the
warmth when I put my fingers in. 'T'o-morrow I will take
the temperature, and I think I will leave her to hatch out the
young. I felt at first inclined to make a preparation of her
and put her in spirits. The pouch entirely disappears, or,
rather, does not appear at all, until the parent is about to lay
her egg. J wish I could send heron to you just as she is.
On placing her in a cask of sand she at once burrowed out
of sight, covering herself with sand to a depth of 4 inches.
“The other specimens which I have also burrow and hide
themselves in comparatively stiff soil. They go often down
4 to 5 feet in the night-time. We dig them out every second
day or so, when we find they have gone too far.
““T hope to be able to make some observations on the length
of time in hatching. Other females which I have have no
eggs inthe pouch. ‘They feed freely on fresh milk, sweetened
with a little sugar, and some bread-crumbs added. Some
become tame very soon, and come readily for their milk;
others wiil not drmk except when one is out of sight.”
(A description of the mammary pouches and mammary
foetus is given in the ‘ Philosophical Transactions’ for 1865,
pp- 671-686, pls. xxxix.—xli.)
480 Prof. M‘Intosh’s Notes from the
XLVII.—WNotes from the St. Andrews Marine Laboratory
(under the Fishery Board for Scotland). By Prof. M‘INTosH,
MAD. ED: he anss:.cc.——_ New ine
[Plate XIIT.]
1. On the Ova of Callionymus lyra, L.
2. On a new British Stawrocephalus.
3. On certain Processes formed by Cerapus on Tubularia indivisa.
4, On Structures resembling Ova procured off the Forth.
5. On a Female Porpoise, with a note on its Milk.
1. On the Ova of Callionymus lyra, L. | .
So little was known about the breeding of this fish that the
most recent work on British fishes, viz. that of Dr. Day f,
contains nothing more than the following remark, the quota-
tion of which will indicate how much remains to be done in
this department :—“ Dr. G. Johnston } recorded having found
a sordid dragonet containing milt or soft roe, it being a young
male. The Rev. G. Harris § mentions having discovered
hard roe in a gemmeous dragonet, which, provided the obser-
vations were correct, is interesting as seeming to show that
the female might assume the colours of the male and still not
be sterile. The observation does not seem to have been con-
firmed by any other naturalist.” It will thus be observed
that the author has nothing to advance in regard to the nature
of the ova or spermatozoa, and nothing in regard to the period
of spawning. Yet the skulpin is a very common fish on our
eastern shores both in the trawl and on the lines of the fisher-
men, since it ranges from a few to 40 fathoms and upwards
on sandy or muddy ground. It is perhaps less frequently
brought on shore than other kinds of unsaleable fishes by
either liners or trawlers, since the spinous rosette at the angle
of the preoperculum causes general detestation; indeed, like
the glutinous hag (Myzine), it is often jerked from the line
into the sea by the fishermen or scooped overboard on a
shovel by a trawler. In and near St. Andrews Bay they are
frequently caught on the hooks of the liners (baited with
mussels) when fishing for plaice and dabs as well as for
haddocks; and I have to thank certain of the fishermen for
this and similar opportunities of examining marine specimens.
* Communicated by the Author, having been read at the Aberdeen
Meeting of the British Association (Section D), 1885.
+ ‘Fishes of Great Britain,’ i. p. 176.
+ Zool. Journ. ili. p. 336.
§ Zool. pp. 2999 and 3118.
St. Andrews Marine Laboratory. 481
A careful watch had been kept on the species throughout
the spring; but it was not till the 12th of June that Mr.
Prince, in my absence, procured a female with the ovaries so
advanced as to give reliable data with regard to the eggs.
Other females in a more or less developed condition were pro-
cured in July. In these the total bulk of the ovaries is by no
means noteworthy, even at the breeding-season. ‘They form
a somewhat cordate mass, bifid in front, but connate poste-
riorly, and, like the spermaries, have a coating of the silvery
peritoneal lining on the surface. Some of the ova were trans-
parent, and thus, though small (‘025 to ‘03 inch in diameter),
appeared to be mature. In their very early condition in
the stroma of the ovaries these ova present a characteristic
appearance (Pl. XIII. fig. 3), for shortly after passing
from the stage of a mere nucleated cell the egg appears to have
a double capsule (PI. XIII. fig. 4), viz. an inner clear coat
probably homologous with the zona radiata of other Teleos-
teans, and an outer one of beautifully-arranged hexagonal
cells. The two divisions just mentioned, however, belong
to one layer, as shown in sections made by Mr. Prince.
About a week later (8th August) a female with more fully-
developed eggs was procured; indeed, the specimen seemed
to have deposited part of its ova, some of which lay externally
around the reproductive aperture. From the pellucid appear-
ance of the eggs in various specimens it formerly appeared
probable that they were pelagic, and the condition im this
example cleared’ up any doubts. ‘The translucent ova are
very small, nearly approaching those of the common dab in
this respect, and thus a very large number are held even by
the small ovaries. When mature each ovum (Pl. XIII. fig. 1)
has a very fine hyaline zona radiata, with a series for the
most part of hexagonal reticulations like those of a honey-
comb. These spaces are not quite uniform in size, but
many are. Some again have four, six, and seven sides,
When the edge of the sphere is examined the septa bound-
ing the reticulations stand out very distinctly, and their
edges show minute strie (Pl. XIII. fig. 2). In transverse
section of the partially developed egg in the ovary (Pl. XIII.
fig. 4) the thickness of the zona radiata is in marked contrast
with that in the fully mature ova. The external reticulations
are imperfectly seen in preparations, as they form a confused
layer from collapse. The exact function of this arrangement is
unknown, but it enables the egg to be distinguished at once
amongst its congeners.
So far as observed, a considerable number of ova, propor-
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 33
482 Prof. M‘Intosh’s Notes from the
tionally to the size of the ovaries, seem to arrive at maturity
simultaneously.
The mussels used as bait were found in the stomachs of
several, while in the intestine Zrophon, hermit-crabs, and
fragments of bivalve mollusks occurred.
2. On a new British Staurocephalus (Staurocephalus
Sibert).
When at Whitstable, in June 1884, I noticed in a small
aquarium belonging to Mr. Sibert Saunders a minute annelid
in considerable numbers, and, as its form seemed unfamiliar,
I got.Mr. Saunders to forward some to the St. Andrews
Laboratory, where they now are. The marine specimens in
the aquarium had been procured from the Whitstable oyster-
beds, in which Mr. Saunders has for many years taken a
prominent interest, so that, in all probability, the species
about to be described haunts the alge and other growths
attached to the shells of the oyster. It is very hardy in con-
finement, not only living but multiplying in a small aqua-
rium, and bearing long journeys without loss.
This form (Pl. XIII. fig. 5), which measures about 8 or
9 millim. in length and about 1 millim. in breadth, including
the bristles, is comparatively pale and semitranslucent, the
internal organs, such as the blackish dental apparatus and
the straw-coloured or greenish alimentary canal, being
visible from the exterior. There are about thirty segments
in the body, exclusive of those devoid of bristles, viz. the
cephalic, buccal, first body-segment, and caudal. The tail is
terminated by two long slender styles provided with palpocils.
The head is horseshoe-shaped, and marked along the anterior
edge by a series of palpocils, which are of considerable propor-
tional length. These organs are broad at the base, taper to
a fine point, and apparently are of great tactile sensibility.
Their motion along the anterior arch of the snout is so lively
that the surface seems to be ciliated. On the dorsum of the
prestomium in front of each anterior eye is a small tentacle
of two segments, the basal shorter than the distal, which is
bluntly rounded and furnished with palpocils similar to those
on the anterior arch. A pair of tentacles having the same
structure occupy a corresponding position on the ventral sur-
face of the snout, but they are more external in position, so
that they project distinctly on each side.
The number of eyes is variable ; two are situated externally,
each occupying a dimple behind the dorsal tentacle. They
are simple pigment-spots, blackish by reflected and pale
St. Andrews Marine Laboratory. 483
brownish by transmitted light. The snout often shows a slight
furrow nearly opposite each eye. On the summit of the pre-
stomium, just in front of the nuchal fold, are a smaller pair of
eyes placed near each other. Occasionally a pigment speck or
two exist in front of these.
The armature of the proboscis (Pl. XIII. fig. 6) consists of
a pair of dark brown or blackish, strongly curved, and sharp-
pointed maxille, behind which an acute posterior process
projects. Six denticles, which probably represent the dental
plates of allied forms, occur beneath and in front of these, each
having a somewhat hoof-shaped outline, the free edge ante-
riorly being finely denticulated. They diminish in size from
before backward, the last having a long and slender. process
which reaches the posterior border of the maxille. The
younger examples, as in the figure, have a smaller number of
denticles. The mandibles have a process or tooth on the
inner edge anteriorly, and the external region or spur is
minutely crenate in front. The shafts are gently curved, like
the letter f, and have a wing-like appendage immediately
behind the anterior region.
Dorsally each foot presents a short cirrus, and ventrally a
somewhat larger one. A long and conspicuous setigerous
process occurs between these just above the ventral cirrus.
The dorsal bristles (Pl. XIII. fig. 7) consist of two or three
long and slightly curved simple bristles, the tips of which
are somewhat flattened and slightly hooked. ‘The ventral
series are compound, the terminal pieces being apparently
simple and slightly hooked (Pl. XIII. fig. 8). A strong spine
supports the fleshy part of the foot.
At first sight it was supposed that the species just described
corresponded with a form discovered by Prof. Langerhans in
Madeira, and which he has termed Staurocephalus minimus *.
The latter, however, appears to differ in the greater length
(antero-posterior diameter) of the head and in the minute
structure of the jaws and bristles. Thus the maxille in the
foreign species wholly differ (if the figures of Langerhans are
to be trusted) in appearance, and none of the pectinate pro-
cesses he showsare to be found in the dental apparatusof Stawro-
cephalus Sibertt. So far as could be made out also the tips
of both dorsal and ventral bristles are simply hooked and not
bifid, as in the species from Madeira. Langerhans mentions
that the Lacydonia miranda of Marion and Bobretzky }, from
the Gulf of Lyons, presents certain resemblances to his
* Zeitschy. f. wiss. Zool. Bd. xl. p. 257, pl. xv. fig. 16.
+ Ann. des Sc. Nat. 6° sér. i. p. 57, pl. vil. fig. 17, &c
30°
484 Prof. M‘Intosh’s Notes from the
Staurocephalus minimus, though he observes that the armature
of the proboscis in the latter at once distinguishes them. It
appears to me, however, that these resemblances are quite
superficial and probably have been suggested by the shape of
the head. The position of the short cephalic tentacles, the
structure of the proboscis, the form of the feet and the bristles,
the structure of the segments following the head, and other
particulars widely diverge, as indeed might be expected in a
form approaching the Hesionide.
3. On certain Processes formed by Cerapus on Tubularia
indivisa.
The members of the domicolous subdivision of the Amphi-
podous Crustacea are characterized by the very general habit
of forming tubes of various kinds, which constitute dwellings
as well as nests for the young, as in the common Amphithoé
and in the Podocert. Others, again, excavate tunnels in
tough clay or mud, like Corophiwm, so abundant in the mussel-
beds of the Kden, or perforate wood like Chelura. The subject
of the present remarks, apparently a species of Cerapus,
closely allied to Cerapus difformis, Milne-Kidwards, and very
prettily barred with red on the antenne, constructs groups of
flexible tubes (Pl. XIII. fig. 9, a, a), which vary in diameter
according to the size of the occupant, on stems of Tubularia
indivisa, very much as Stimpson describes in his Cerapus
rubricornis on the shores of Grand Manan. Instead of being
formed, however, as Stimpson says, of ‘ fine mud and some
animal cement,” those of the British species have in addition
grains of sand, bristles and spines of annelids, hairs of sea-
mice, and many fine horny fibres, apparently derived from the
byssi of horse-mussels.
On the same stems of Yubularta supporting the nests or
tubes are certain remarkable processes (Pl. XIII. fig. 9, 6, d)
which project from the coencecium like branches, and, indeed,
it was the unusual appearance and somewhat symmetrical
arrangement of these that first attracted notice. These fila-
mentous branches are of a dull greyish hue (that of the mud),
and are very slightly tapered distally. The basal region,
however, is distinctly larger, especially where fixed to the
zoophyte. Their length varies from 3 to 4 inches, and all
seemed incomplete. ‘hey are smoothly rounded and resemble
the fine muddy tubes formed by certain annelids; but they
are quite solid and composed of the same constituents as the
tubes formerly mentioned, though, perhaps, the foreign bodies,
such as bristles and spines, are more conspicuous. These,
moreover, are neatly arranged with their long axis parallel to
St. Andrews Marine Laboratory. 485
that of the process, and especially abound towards the base of
the filament, which thus is more rigid and tougher than the
distal region, into the composition of which mud, sand, and
the secretion chiefly enter. In consequence of this structure
the distal region slightly curves downward in the ordinary
position in the water, while the proximal stands stiffly out-
ward. ‘These processes are generally fixed to the main stem
of the Tubularia, though occasionally they spring from the
tip of a young example attached to the former, or stretch from
the extremity of a parasitic Sertularian.
These filamentous processes are usually at some distance
from the nests or tubes of the Crustaceans, which climb
actively on them. Whether they thus give them a larger area
for the capture of prey in security or afford a more extensive
surface for the temporary arrest of minute larval or other
forms on which they feed is unknown. It is probable, how-
ever, that processes so elaborate subserve some useful purpose
to the species, and are not the result of mere purposeless
formation by way of exercise. ;
Spinous processes of an equally peculiar kind are not un-
common on the tubes of annelids, such as those of Nothria
Willemoestt and certain Terebellide discovered by the ‘ Chal-
lenger.’ Most of these, however, have a protective function,
whereas the foregoing processes cannot have this use assigned
them.
4, On certain Structures resembling Ova procured
off the Forth.
When carrying out the work for H.M. Commission on
Trawling an old willow basket came up in the net on the
15th August, 1884, 15 miles S.H. of the island of May,
which, besides other interesting marine forms, had attached
to it certain peculiar dull yellowish structures resembling ova,
and about 4 inch in diameter (Pl. XIII. fig. 10), They adhered
to each other, forming a group in asingle layer along the bark
of the twig. ‘They are nearly circular, with a short, slightly
curved distal process. ‘The capsule is yielding, but tolerably
tough, and the contents consist of a structureless soft and cohe-
sive gelatinous substance of a pale colour. ‘They were kept for
a considerable time in the marine laboratory of St. Andrews,
but no change ensued until decomposition set in.
5. Note on a Female Porpoise and its Milk.
Amongst the porpoises examined during the year at the
marine laboratory was a fine adult female abounding in milk.
For some days before its capture, in August, a solitary adult
486 Notes from the St. Andrews Marine Laboratory.
individual had been noticed disporting itself in circles close
to the commencement of the East Rocks, and it is possible
that this was the specimen (5 feet 2 inches in length) cap-
tured in the salmon-nets. It had evidently been suckling,
and a small quantity of its milk was preserved for examina-_
tion. The mammz were very prominent on capture, pro-
jecting beyond the suleus in each case, but in ten or
twelve hours after death they had shrunk very considerably.
The milk is of a dull yellowish colour and of the con-
sistency of thick cream, so that it passed with difficulty
through the neck of a bottle. In John Hunter’s “ Obser-
vations on the Structure of Whales’’*, it is stated of this
species that ‘the milk is very rich; for in that caught near
Berkeley with its young one, the milk, which was tasted by
Mr. Jenner and Mr. Ludlow, surgeon, at Sudbury, was rich,
like cow’s milk to which cream had been added.” I have to
thank my colleague, Prof. Purdie, for making the subjoined
‘¢ Note on the Chemical Composition of the Milk of the Por-
poise” from a small quantity collected chiefly from the re-
servoirs during the dissection +.
The specimen appeared to have been delivered at a com-
paratively recent period, so that the remarks in the last
edition of ‘ Bell’s British Quadrupeds’ may be supplemented.
It is stated that a female was found pregnant towards the end
of the year; and again, that Mr. Jenyns found a female in
May with a fully-formed young one. They probably produce
their young chiefly in summer. In the stomach of the ex-
* IT am indebted to Prof. Flower for drawing my attention to this
paper. ‘ Works of John Hunter’ (J. F. Paimer), vol. iv. p. 392, edited
by Sir Richard Owen.
+ “ Prof. M‘Intosh having kindly placed at my disposal a specimen of
milk which he extracted from the mamme of a porpoise, I have made an
analysis of it, thinking that the results are not without interest.
In 100 parts by weight.
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Malkesugari(?)i> caterer anseeemts 1:33
Mineral salts) scarce Seton 0:57
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“The most remarkable point about the composition of the milk is the
large percentage of fat it contains, a constituent of food which, I presume,
the cetacean, from its mode of life, would require in larger proportion
than ordinary mammals do. The milk was not of an inviting appearance,
being of a yellow colour and thick consistency, and possessing a
‘ fishy’ smell. The specific gravity of the milk, in spite of its solid
contents, differed little from that of water.”
(Vide Chemical News, 2nd Oct. 1885.)
On the Nest and Development of Gastrosteus spinachia. 487
ample caught at St. Andrews was a mass consisting of a
number of herrings, “small” whitings, and haddocks.
EXPLANATION OF PLATE XIII.
Fig. 1. Mature ovum of Callionymus lyra, L., somewhat darkly shaded,
and slightly altered (from keeping) inferiorly. Magnified.
Fig. 2. Honeycomb-like arrangement of the surface of the same. More
highly magnified.
Fig. 3. Immature egg of the same from the ovary. Magnified.
Fig. 4. Section of an immature ovum in the ovary. The areolated super-
ficial layer of the zona radiata presents a confused appearance
externally, from collapse in mounting.
Fig. 5. Young example of Stawrocephalus Siberti, n. sp. The eyes are
absent in this example. Enlarged.
Fg. 6. Dental apparatus of the foregoing. x 90 diam.
Fig. 7. Dorsal bristle of the same. X 350 diam.
Fig. 8. Ventral bristle. x 350 diam.
Fig. 9, Stem of Tubularva indivisa with crustacean nests (a,a) and filamen-
tous processes (4, 6) attached to the chitinous periderm. About
natural size.
Fig. 10. Structures resembling ova attached tu a fragment of willow.
Slightly enlarged.
XLVIII.—On the Nest and Development of Gastrosteus spina-
chia at the St. Andrews Marine Laboratory. By EDWARD
HK. PRINCE.
[Plate XIV. ]
A COMMUNICATION to the Biological Section of the British
Association at its recent meeting embodied certain observa-
tions made during the past summer at the St. Andrews
Marine Laboratory, and of this the present paper is an ampli-
fication. Gastrosteus spinachia, amongst the smaller Tele-
osteans occurring upon our coasts, is a very common though a
highly interesting form. Various authors, Kupfer, Ransom,
Mébius, and others, have treated of this or the allied fresh-
water species ; but the notices of the nidification, development,
&e. of the marine form are very fragmentary and incomplete.
During the summer of 1885 a large number of the nests of
the fifteen-spined stickleback have been examined in the St.
Andrews laboratory; the process of building has been
watched and the early stages of development studied.
Towards the latter end of April and during the months of
May and June these nests may be found in sheltered rock-
pools, between tide-limits, and generally some distance from
low-water mark, so that, as Dr. Day observes, “ they may be
left uncovered for two or three hours at a time.”* They
* Hist. of Brit. Fishes, p. 248.
488 Mr. E. E. Prince on the Nest and
occur most frequently amongst sea-weeds fringing tidal pools,
and of such marginal weeds they are constructed. Prof.
Mobius states * that the nests vary from 2 to 3 inches
(5 to 8 centims.) in diameter ; but these dimensions are often
exceeded, the size being very variable and depending on (1) the
character of the materials employed, and (2) the number of
fishes depositing their ova in a particular nest. It is remark-
able that the eggs of more than one female may be deposited
in a single nest. ‘This actually took place in the tanks of the
laboratory—a female taking possession of an old nest, which
contained advanced ova, and upon completing oviposition in
the lower part of the nest, the male immediately surrounded
that portion with binding threads. That the number of ova in
one nest is often greater than a single female produces has
been noticed by many observers ; and Couch, struck by their
disproportionate bulk, said that it was ‘ only to be explained
by the well-known fact that the ova of fishes generally obtain
an increase of bulk by the absorption of water after ex-
clusion” +; but the enlargement of non-pelagic eggs with
dense capsules is not sufficient to account for the phenomenon
in question, and the explanation is to be found in the plurality
of females resorting to a particular nest. The male fish,
which is the nest-builder, often selects a growing mass of
Fucus-fronds, projecting 8 or 10 inches from the rock, and
having a diameter of 5 or 6 inches in the widest part (Pl. XIV.
fig. 5). A bunch of more minute Alge, e.g. Ceramium,
Corallina, &c., may be chosen, and the nest assumes a less
cylindrical and more spherical form, measuring from 3 to 5
inches in diameter. In the former case little labour is required
in building, the male merely binding the fronds by delicate
circumscribing threads, which pass round transversely to the
long axis of the mass (Pl. XIV. fig. 5, a, a). In the latter
case, in which softer and less coarse materials are used, much
labour is involved, the growing tuft forming merely the basis
upon which the gathered fragments of Algee, Ulva, Corallina
officinalis, Hydrozoa, &c. are woven ; this heterogeneous collec-
tion of dead fragments being intermingled with the fronds of
the living plant and secured by tenacious threads, so that a
somewhat compact mass is formed (Pl. XIV. fig. 5). The
nest 1s pendulous and, being firmly anchored, is swayed about
by the movements of the tide. So compactly are the mate-
rials interwoven that it is often difficult to tear them asunder,
though they are always so disposed as to leave interspaces
which are enlarged into more capacious chambers by the
* Vide Note in Aug. part (1885) of this Journal, p. 153,
+ Couch, Hist. of Fishes of Brit. Islands, vol. iii. p. 182.
Development of Gastrosteus spinachia. 489
motions of the fish, the snout bemg introduced and worked
about until pocket-like cavities are formed, or the creature,
as often happens, passes and repasses through the cavities
with similar results. The thread-like material which binds
the nest is a remarkable product. It is secreted by the male,
is colourless, tenacious, of the consistency of mucilage when
freshly extruded, and exhibits a delicate blue opalescence
which disappears in two or three days, leaving the threads of
a transparent grey or dirty-white colour. According to Mobius
it is nitrogenous, as is shown by treating with acids and
alkalies, and evidently a form of mucin peculiarly modified.
Like normal mucin it is gelatinous and viscid in water, turn-
ing white like tallow on immersion in spirit. Carmine stains
it deeply.
On examining the male at the breeding-season, the kidneys
are seen to be considerably swollen, the enlargement being
especially noticeable posteriorly (fig. 14). Sections of
the kidneys reveal an altered condition of the sinuous tubules
(fig. 1 A, 6), the conical epithelial cells of which are swollen at
their free ends and indefinite in outline. The nucleus of each
cell is slightly displaced and occupies a more terminal posi-
tion than in the normal condition. These epithelial cells are
active in secreting the material used in constructing the nest.
They perform the function, indeed, of cell-glands, and their
secretion is carried by the uriniferous tubes to the outer ven-
tral border of each kidney, where a large duct passes longi-
tudinally. In cross section the ureters (Pl. XIV. fig. 1 A, a, a)
are oval, and their capacity is very great at this time, the
walls being of dense fibrous tissue lined with pavement
epithelium. Both ureters emerge from the renal mass near
the posterior end and, descending in a forward direction, be-
come applied to the wall of the so-called urmary bladder, which
at this point is somewhat attenuated, and, passing anteriorly,
they open obliquely from without inwards into the bladder.
This structure, it is unnecessary to say, is not morphologically
connected with the urinary receptacle of higher Vertebrates,
the lengthened course of the ureters, of which it is simply
a dilated common portion, being due to its extraordinary de-
velopment in the male stickleback. In a fish 54 inches in
length it is about an inch long, and at its widest part + inch
in diameter. Situated on the right side of the abdominal
cavity, immediately below the swim-bladder in the post-
hepatic region, it has the form of a capacious pyriform
sac, ending blindly anteriorly, and diminishing in circum-
ference as it passes backwards (Pl. XIV. fic. 6,2). Be-
fore terminating posteriorly it describes a double curve,
490 Mr. E. E. Prince on the Nest and
crossing over the intestine from the right to the left side
(Pl. XIV. fig. 6, 6), and after a short parallel course passing
on the ventral side of the intestine to the right side again
(Pl. XIV. fig. 6, c), debouching behind the genital pore
(Pl. XIV. fig. 6, d) into a urinogenital sinus, forming the
posterior portion of a cloacal depression (Pl. XIV. fig. 6, e),
into which also the anus opens (PI. XIV. fig. 6, 7). The wall
of the bladder consists of two layers, an internal epithelium
(Pl. XIV. fig. 1 B, a), which is readily detached, and a
dense external connective layer (Pl. XIV. fig. 1 B, 6), which
thins out as the bladder enlarges anteriorly. Traces of an
intermediate muscular layer appear posteriorly where the
walls are extraordinarily thickened. ‘The descending ureters
(Pi. XIV. fig. 1 B, ¢ c) approach opposite sides of the
bladder, that on the left proceeding obliquely below the
common duct of the vasa deferentia, and passing forward
and merging in the walls of the bladder on the left side. This
union is shown in the same transverse section which shows
the union of the vas deferens of the left testis with that of the
right. The course of the right ureter is shorter and more
direct, as the bladder lies on that side of the abdominal cavity
at this point. It coalesces with the right wall of the bladder
precisely opposite the left ureter. As the bladder descends
to cross the intestine inferiorly it twists, so that the left
ureter is brought to the ventral side and the right ureter
ascends to the dorsal side of the cervix of the bladder. Both
return to the lateral position as the bladder crosses the intes-
tine. The intestine now curves to the right, and the relations
of the ureters become reversed, the right being below and the
left rising to the dorsal side of the bladder. They increase
rapidly in capacity, showing in cross section an extremely
elliptical cavity, and as the bladder enlarges they pass
obliquely into its chamber, their walls being continuous with
the external layer of the bladder. Along this tortuous course
the viscid secretion of the renal tubules reaches the bladder,
where it is stored up. When first formed the secretion is
simply a plastic jelly; but a fibrillar structure appears to
rapidly develop in it. Indeed this appearance is assumed
while the secretion is contained in the ureters. ‘The epithelial
cells of the urinary canals exert so actively the secreting func-
tion that the bladder becomes much distended by the accumu-
lating mucus, and at length it flows slowly to the urinary
aperture, where it emerges as a tenacious elastic thread which
readily adheres to any external object on contact. It can
hardly be doubted that this secretion can be extruded at
pleasure, the walls of the bladder assisted by the abdominal
Development of Gastrosteus spinachia. 491
parietes being sufficient to effect this; but it is produced so
abundantly that it also often appears to ooze out involun-
tarily. Male fishes may often be seen with a glistening,
pendulous, conoid mass hanging from the urinary aper-
ture, and increasing in size until it becomes detached.
Such flask-shaped masses of mucus occur frequently in
tanks where these fishes are confined and no opportunity is
afforded for nest-building. When, however, an appropriate
mass of sea-weeds has been selected by the male, the fish
has merely to approach closely, so that the protruding
mucus may adhere to a projecting frond, and by passing and
repassing round the mass the weaving operation is accom-
plished *. Occasionally a rapid ejaculatory movement is
observed, and it is interesting to note that the threads are not
carelessly superposed, except when necessary for increasing
the density of the nest, but are crossed at an angle by the
varying movements of the fish, so that rhomboidal spaces
are enclosed and a regular reticulum is thus produced
(Pl. XIV. fig. 5).
Often the tightly-drawn thread snaps asunder, though its
tenacity is extreme; the fibres then curl up and form a ter-
minal pellet, many of which occur on the surface of the nest.
As before remarked, the mucus is not merely a semi-solid
plasm, but assumes a funicular character while in the ureters,
If one of the cords binding a nest together be examined it
will be found to consist of several strands, the cord itself
measuring from ‘0046 inch to ‘0051 inch in diameter, and the
constituent threads from *0008 inch to ‘00092 inch. These
smaller threads again consist of fine homogeneous filaments,
which adhere in parallel order. The parallel arrangement of
the ultimate fibrils 1s very striking and quite characteristic
(Pl. XIV. fig. 4).
On the completion of the nest the female deposits the ova
in the various chambers (Pl. XIV. fig. 5,66). The ovum
is disproportionately large, viz. ‘085 inch in diameter, rarely
spheroidal, the form being generally an ellipsoid. ‘The cap-
sule does not harden for several hours, its soft tenacious
nature, assisted by the ovarian fluid, causing the ova to
adhere strongly together. Indeed, after being separated,
these ova, when brought into contact again within a few
hours, immediately cling firmly to each other. As just
* The interesting behaviour of the male fish at this time has been
described by many observers. His solicitude for the safety of the ova,
and especially for the young when hatched, is very remarkable: vide
Ransom, this journal, vol. xvi. 1865, p. 449; also G. J. Romanes,
‘ Animal Intelligence,’ pp. 248-245, >
492 Mr. E. E. Prince on the Nest and
observed, this tenacity is increased by the fluid secreted by
the ovary, which slowly hardens when exposed to sea-water,
and the ova are bound strongly in irregular masses. They
cannot be separated save by exerting some force, and distinct
facets or scars upon the capsule mark the points of attach-
ment to neighbouring ova. Small spaces are left between
adjacent ova, and the mass thus possesses a porous or spongy
character, a feature of great consequence, to which attention
was first drawn by Prof. M‘intosh in the June part of this
journal. In describing the ova of Cottus bubalis Dr.
M‘Intosh said, “All adhered firmly together, yet leaving a
series of cavities, so that the whole mass, as in Cyclopterus,
imbibes and retains water, a provision of importance in
the case of eggs deposited near low-water mark ” *.
When newly extruded the ova exhibit a delicate pale-
green hue, which, however, soon gives place to the
characteristic translucent amber tint. ‘The capsule is hya-
line, very dense, and resistent, the thickness being ‘0013
inch, and it is separable into lamelle. In microscopic section
from twenty-five to thirty strata can be distinguished, and upon
roughly tearing the ewe the successive lamellz are
readily seen (Pl. XIV. fig. 2). The capsule is minutely
PSS the pits being sate in parallel rows (Pl. XIV.
fig. 2). The micropyle is very distinct, and exhibits the
usual funnel-like form, bold striz radiating from the external
aperture and giving it a stellate outline when viewed from
above. A large mass of pale yellow oil-globules are age're-
gated at the vegetative pole and maintain usually a position
in the segment opposite the germinal pole. About two
hours after fertilization the protoplasmic cap is formed, and
cleavage proceeds in the usual manner, the 16-cell stage being
completed about the twelfth hour. ‘The morula is reached at
the thirtieth hour, and the periblast is then boldly marked,
though no nuclei are apparent. In cross section the usual
triangular form of the periblast is seen. The disk occupies
the under side of the deutoplasmic globe; but if the ovam be
shifted so that the disk becomes uppermost, it occasionally
remains in that position, or, as is usual, regains its normal
position slowly, and apparently with ‘difficulty, the oil-
globules having little power to “right” the disk. Delicate
filaments, often very numerous, connect the mass of globules
with the under surface of the disk. Similar pseudopodial
threads were noted in Zinca by EH. van Beneden, and in
Gastrosteus aculeatus and G. pungitius by Ransom.
* Ann, & Mag. Nat. Hist. June 1885, p, 433.
Development of Gastrosteus spinachia. 493
The course of development is very slow as compared with
pelagic ova. It was not until the fourth day that nuclei
became visible in the periblast, and the corneous layer differ-
entiated from the “ lower layer” cells. On the sixth day the
marginal rim is defined and the embryonic scutum indicated,
the embryonic thickening being also apparent about noon on
that day, by which time the blastoderm invests barely one
third of the yelk. By the eighth day two thirds of the yelk-
surface are enveloped, and the blastoderm is somewhat de-
pressed. ‘The portion of the yelk-surface not yet invested is
dotted (with some approach to regularity) with nuclei.
Round each nucleus, which is multinucleolate, protoplasm
gathers and sends out radiating pseudopodia. Large cells
also occur and refringent particles are abundant. Meanwhile
the cephalic portion of the embryo is increasing in thickness,
so that the keel prominently projects on the ventral blasto-
dermic surface; the optic vesicles are rudely indicated, and
the neurochord is differentiated, growing down as the noto-
chord appears; and before the close of the eighth day the
mesoblastic plates are well defined. The blastoderm, external
to the embryo, assumes a striking appearance, as clear vesicles
can be discerned scattered numerously over it. These nuclei,
possibly periblastic, have a rounded outline and exhibit
several nucleoli. Kpiboly continues during these changes,
and on the twelfth day the closure of the blastopore is effected.
Many of the nuclei just noted now approach each other and
coalesce. Segmentation of the embryonic trunk proceeds
rapidly, and on this day twelve protovertebree are marked off.
On the following day (the thirteenth) four more are segmented,
the primitive optic vesicles are pushed in, and the lenses
developed ; the otocysts also appear ; the nasal pits are distin-
guishable and the cranial divisions are rudely marked. B
the fourteenth day the embryo has appreciably lengthened ;
Kupter’s vesicle (which appears just before the closure of the
blastopore, and attains its maximum shortly after) still per-
sists, though reduced in size; the cranial region is greatly
advanced, an enteric strand of cells is being aggregated in
the mid-ventral region, and nineteen protovertebre can be
counted. A pectoral swelling is visible, indicating the
growing heart. This organ rapidly develops, and by the
seventeenth day assumes its characteristic campanulate shape.
By the dehiscence of the yelk and the splanchnic mesoblast of
the embryo a chamber is formed round the heart. At this
time the caudal end of the young becomes free, the embryonic
fin passing as a median membrane along the dorsum round
the termination ot the tail, along the ventral ridge, to the anal
494 Mr. E. E. Prince on the Nest and
area. The eyes, in which the lenses are now fully formed,
are faintly pigmented with black. Nuclei still persist over
the blastoderm, probably periblastic, but they are much
reduced in number. Before the close of the seventeenth day
the heart pulsates, though slowly and irregularly; more
rapidly, however, on the eighteenth, though no hemal fluid is
as yet visible.
On the nineteenth day a distinct circulation is active. The
formation of circulatory channels on the yelk-surface is very
readily seen, and coincides with Ryder’s description of the
embryo of Apeltes*. ‘The venous end of the heart, as in all
Teleosteans, is applied to the yelk-surface, and by an exca-
vation in the latter a capacious sinus is formed, in which
corpuscles are seen vibrating to and fro, with the cardiac pulsa-
tions, before a circulation has commenced. Whether these
primitive corpuscles originate in the periblast was not deter-
mined; but it certainly is the case that periblast-cells are
detached and pass with the hemal fluid into the heart when
the circulation is established. This accords with Ryder’s
contention (in common with Hoffman, C. Vogt, and others)
that the blood is a derivative from the periblast.
The vascular trunks, ramifying over the vitellus, appear to
be simple lacunz hollowed out of the yelk-cortex. In addi-
tion to the circulation of the embryonic trunk proper, the
subnotochordal, arterial, and the cardinal (venous) trunks
(which extend no further than the root of the tail at this stage),
there are a subintestinal vein, breaking up apparently in the
liver, and two large vitelline vessels. Of the last-named,
one emerges behind the heart and the other in the region of
the hind gut, the alimentary canal as yet ending blindly.
These two capacious vitelline trunks unite in the distal por-
tion of the yelk and return by a common large vein, which is
joimed by numerous lesser trunks, until it reaches the pectoral
region, where it pours its volume into the sinus communicating
with the heart.
A complex network of blood-vessels, or, rather, of sinuous
lacune, covers the deutoplasmic globe, and the early approach
of the hatching stage is indicated. On the nineteenth day,
indeed, the embryo is very restless, the tail being spasmodi-
cally flexed and straightened, and vigorous side-to-side move-
ments are executed. ‘The pigment of the eyes is more dense,
though the trunk is comparatively free from pigment, a few
non-stellate black spots merely occurring on the dorsum. The
development of the liver and alimentary canal agrees with
* U.S. Fish Comm. Report, 1882, p. 548.
Development of Gastrosteus spinachia. 495
that of Teleosteans in general. The swim-bladder can be
made out immediately beneath the notochord ; but no anal or
urinogenital structures can be clearly distinguished. By the
twentieth day the heart has lost its simple tubular structure,
and, as a thin-walled sac, is flexed upon itself; and on
the twenty-first day the circulation is in vigorous action, a
great volume of corpuscles surging through the yelk-trunks.
It is not proposed to make reference to the serial micro-
scopic sections of embryos which were prepared during
these observations, as space will not permit, and the prepara-
tions have not yet been completely worked out in the labora-
tory. It must suffice in this brief survey of the early stages
of Gastrosteus spinachia to note that the embryos emerge at
various dates from the twenty-fifth to the fortieth days after
fertilization—this variation in series of ova deposited at the
same date being due to their unequal rate of development, the
more central ova being longer, and the external ova being more
rapid in reaching maturity. The newly-hatched young are
soon richly supplied with pigment, bright yellow spots being
scattered over the surface of the trunk, especially the dorsum,
and elaborate stellate black pigment-spots occurring on the
dorsal and lateral regions. ‘They are very vigorous and
active, contrasting greatly with the frail embryos of our
common food-fishes, whose ova are pelagic.
It may be noted that the temperature of the water in the
tanks during these observations varied from 41° F.in May
to 50° or 51° F. early in June. The unique situation of the
St. Andrews Marine Laboratory and its natural conditions
being unusually favourable for the development of the ova of
marine fishes, the phenomena observed in the progress of
Gastrosteus spinachia may be taken as almost normal.
P.S.—It is remarkable that, whereas in the freshwater
sticklebacks the male during the breeding-season assumes
brilliant colours, the pectoral and ventral region being of a
bright scarlet tint, in the marine species no such distin-
guishing marks appear. Both sexes exhibit a similar marking.
The male alone appears to construct the nest, and though
female fishes, distended with eggs, often hover near during
the building process, none were observed at St. Andrews to
take any part in the work. ‘The statement published by
Heincke * that the male and female fishes build the nest is
probably incorrect and due to the similarity of the hues of
both sexes.
* ‘Tllustrirte Naturgeschichte d. Thiere’ (Leipzig, 1882), p. 400.
a
496 Dr. H. A. Nicholson and Mr. A. H. Foord on
EXPLANATION OF PLATE XIV.
Fig. 1. Transverse section (male Gastrosteus sp.) of renal mass, urinary
bladder &c. im situ, x 150 diam. A, Iidneys (coalesced por-
tion): a, a, right and left ureters passing longitudinally along
outer ventral borders of kidneys; 6, urinary tubules, nuclei of
epithelial cells indicated. B, urinary bladder, behind the cervix:
a, epithelium ; 6, fibrous layer; c, c, right and left ureters (on
opposite sides of bladder); d, contained thread-like secretion
from kidneys ; C, intestine ; D, D’, testes.
Fig. 2. Fragment of hyaline capsule of ovum, showing the rows of pits
and lamellee, x 500.
Fig. 3. Ditto, in transverse section, showing numerous lamelle, x 350.
Fig. 4. Portion of mucous secretion, showing funicular structure, xX 350.
Fig. 5. Sketch of nest (diagrammatic), one third nat. size, the pockets
containing ova exposed. a, a, transversely-arranged inter-
secting threads; 0, 6, masses of ova contained in the interspaces
of nest.
Fig. 6. Dissection of male, showing viscera of posterior portion of abdo-
minal cavity, about nat. size. a, enlarged urinary bladder; 6,
left flexure of ditto (cervix); ¢, right flexure of ditto (near
posterior termination); d, genital pore; e, cloacal depression ;
j, anus; g, urinary aperture; A, alimentary canal; 2, 2, right
and left testes; 7, 7, kidneys; j1, ureters; &, swim-bladder.
XLIX.—On the Genus Fistulipora, M‘Coy, with Descrip=
tions of several Species. By H. ALLEYNE NicHoxson, M.D.,
- D.Sc., Regius Professor of Natural History in the Univer-
sity of Aberdeen, and ArTHuR H. Foorp, F.G.S8., late of
the Geological Survey of Canada.
[Plates XV.-XVIIT.]
INTRODUCTION.
In the course of our study of various species of /¢stulipora
a most interesting and suggestive structural feature has come
under our observation. ‘This consists of a very peculiar
modification of the walls of the autopores*, which gives them
quite a distinct. faczes, and as it appears to have an important
bearing upon the question of the zoological affinities of the
genus (and consequently upon that of the Monticuliporide in
general) we shall describe it as minutely as possible.
* We avail ourselves of this opportunity to offer a few words of expla-
nation to the reader with reference to this and other terms we have found
it expedient to introduce in substitution for the older ones hitherto in
use. The principal tubes in F’stulipora and other genera of the Monti-
culiporidee have been called “large corallites,” or simply “ corallites ;”
the tubes or tubuli filling the interspaces among these received the name
of “ interstitial tubes ;” while the minute tubuli situated at the angles of
the Genus Fistulipora, M‘Coy. 497
In well-preserved specimens, with the aid of a lens, the
autopores are seen to possess a strong fold or sinus on one
side of the cell-aperture, raised above the general surface
(woodcut, fig. 2). That this fold is not superficial is proved
by the fact that it occurs at all levels in the corallum at which
a section may be made. Itis seen also in longitudinal sec-
tions throughout the whole length of the autopores. In a
transverse section this fold imparts a trilobate or floriform
junction, or in other parts of the thickness of the walls, of the other tubes
were entitled “spiniform corallites” (H. Alleyne Nicholson, ‘ Paleeozoic
Corals,’ Monticulipora, 1881, chap. ii.). Finding these terms incon-
venient for purposes of description, we propose to substitute for them the
following :—Autopores (=“ large corallites”), Mesopores (=“ interstitial
tubes”’), and Acanthopores (=“ spiniform corallites”).
The term “corallites ” will be used only in a general sense when refer-
ring to the tubes of which the colony is made up.
Fig. 1. Fig. 2.
Fig. 1.—A few coraliites of F. eriensis, Rom. : a, autopores; m, meso-
pores ; ac, acanthopores. Enlarged about forty times.
Fig. 2.—a. Profile view of a portion of the surface of Dekayia aspera,
Milne-Edw. & Haime (also one of the Monticuliporide), to show acan-
thopores ; 6, the same viewed from above. Enlarged about forty times.
There are two other words we shall have occasion to employ in the de-
scriptions that follow; these are “monticules” and “macule.” They
have been used by one of the writers (doc. cit.) and by other authors to
designate those minute areas or spots, either raised above the general sur-
face of the corallum (monticules) or alittle below it, or on a level with
it (macule), which constitute the characteristic ornamentation of the
Monticuliporidze. It seems evident that these “ macule ” and “monti-
cules” (consisting sometimes of cells larger than the average size of the
corallites) are centres from which the growth of the colony proceeded.
As illustrating this suggestion the reader is invited to look at the trans-
verse section of Fstulipora utriculus, Rominger (Pl. XVI. fig. 1c), which
shows (in section) one of these spots, in this instance composed of meso-
pores ; and the autopores, with their folds directed inwards, surrounding
it. This condition of things subsists throughout the entire colony. Had
the section been made larger it would have shown that similar areas occur
adjacent to each other, thus presenting a series of “macule,” around |
which the autopores range themselves in concentric rows.
Ann. & Mag. N. Hist. Ser. 5. Vol. xvi. 34
498 Dr. H. A. Nicholson and Mr. A. H. Foord on
aspect to the cells (Pl. XVI. fig. 1c), interrupting the conti-
nuity of their outline and forming by its free ends two tooth-
like projections in the interior of the cell. It will be noticed
that the fold is of a lighter colour than the other part of the
cell-wall. This lighter portion consists of crystalline calcite
of a similar character to that of the matrix or infilling of the
cells, though very slightly darker, while the remaining portion
of the cell-wall and the walls of the mesopores are composed
of a dense, granular, opaque calcite. This difference in the
mineral composition in the two parts of the cell-wall must
certainly have originated in the living tissues of the organism,
because the same phenomenon is met with in species from
such widely separated localities as Canada and Westphalia.
Concerning the morphological significance of the peculiar
modification of the cell-wall we have just described, a valuable
suggestion has been made to one of the writers by Prof.
H. N. Moseley and Mr. G. B. Howes, after examining many
specimens and sections of Fistulipora, to the effect that these
structures may have formed a portion of the endo-skeleton
supporting in the animal a ciliated groove (siphonoglyphe)
similar to that which is found in the stomodeum of the
Alcyonarians*.
This suggestion seems in our judgment to yield the only
explanation which, in the present state of our knowledge, can
be afforded in reference to this most interesting question. Some
further observations upon it, however, appear to be needful.
We have seen that the folds in Mstulipora are present only
in the autopores (= autozooids of the Alcyonarians ?) and not
in the mesopores (=stphonozooids of the Alcyonarians ?).
Their strong development in the former may be explained by
supposing that the mesopores, becoming aborted, threw upon
the autopores the task of supplying by their strong cilia the
circulation of sea-water requisite for the nourishment of the
colony. The peculiar condition of the mesopores in Mistulipora
lends support to this view, as the close vesiculose tabulation
which characterizes them would be difficult of explanation
upon any other hypothesis.
With reference to the (assumed) occurrence of such a
strongly marked ciliated groove in the autopores of the F%s-
tulipora-colony it may be alleged that this is a somewhat
rare condition to meet with in living Alcyonarians; but it is
not altogether wanting in that group, for we find in the genus
Sarcophyton (a dimorphic form) that the autozooids possess a
* Sydney J. Hickson, “ On the Ciliated Groove (Siphonoglyphe) of the
Stomodeum of the Alcyonarians,” Phil. Trans. Royal Soc. part 111. 1888.
the Genus Fistulipora, M‘ Coy. 499
siphonoglyphe, though it is not so well marked as in the
siphonozooids*. |
We must not overlook the fact, however, that in Sarco-
phyton the siphonoglyphe is present only along the inner
third of the stomodeumt, whereas in F%stulipora the fold,
which we have assumed to have supported this ciliated groove,
extends uninterruptedly throughout the entire length of the
autopores, and, moreover, it appears upon the surface of the
corallum in the form of a prominent arched lip in the apertures
of those cells.
__ The occurrence of folds in the walls of the autopores of the
Fistulipore has been observed by Dr. Rominger{, of Ann
Arbor, Michigan, who, however, does not appear to have
attached any importance to it. Though unaccompanied by
figures his descriptions are generally of sufficient exactness to.
enable the species to be identified. One of them, Mistulipora
utriculus, is described and figured in this article. One of the
writers has also noted and illustrated the structure in question
in Fistulipora incrassata§. Mr. Ulrich of Cincinnati has
published descriptions of a number of species of Hstuliporal| ;
but he makes no mention of folds in the walls of the autopores,
the apertures of which he figures as rounded or oval in out-
line with more or less thickened margins. His omission of
the folds in the autopores is not difficult to account for, as
when not distinct they may be easily overlooked, especially
in sections which have not been cut exactly at right angles to
the longer axis of the corallites. The folds are represented,
however, in an unmistakable manner in a figure Mr. Ulrich
gives of Lichenalia concentrica, Hall{], and they form the
‘subject of some remarks upon the genus Lichenalia, which
are here condensed. Mr. Ulrich proposes to eliminate from
the genus Fistulipora, and place in Lichenalia, those species
possessing “thin, lamellate, or bifoliate zoaria, and more or
less distinctly bidenticulate apertures” [=folds]. As, how-
ever, Mistulipora imcrustans, the type of the genus Pistule-
pora, possesses such “ bidenticulate apertures” as one of tts
most marked characters, it is clear that Mr. Ulrich’s proposal
cannot be entertained, and that Lichenalia, as he has charac-
terized it, is a Mistulipora.
It has now become necessary to give a new diagnosis of the
genus Histulipora, so as to introduce into it the peculiar struc-
tural features which we have been dwelling upon.
* Loc. cit. p. 695. + Ibid.
t Proc. Acad. Nat. Sci. Philadelphia, 1866, p. 113.
§ H. A. Nicholson, Pal. Tab. Corals, 1879, p. 308.
|| Journ. Cincinnati Soc. Nat. Hist. vol. vii. April 1884, p. 43.
q Loe. cit. pl. iii. fig. 5.
34*
500 Dr. H. A. Nicholson and Mr. A. H. Foord on
Genus Fistutrpora, M‘Coy, 1849, emend.
Nicholson & Foord.
Corallum variously shaped, dimorphic ; consisting of two,
more rarely of three, kinds of corallites; the first series
(autopores) of a cylindrical or subcylindrical form with distinct
walls, which on one side are thrown into two more or less
well-developed longitudinal folds, giving to the cross section
of the tube a characteristic trifoliate form. Apertures with
raised margins, and prominent arched lips on one side corre-
sponding with the folds. ‘Tabulee numerous, horizontal. The
second series (mesopores) generally numerous, with imper-
fectly developed walls and very abundant tabule, which by
their coalescence give rise to a vesicular tissue*. The third
series (acanthopores), sometimes absent, consist of very minute
tubuli, situated at the angles of junction, or in other parts
of the thickness of the walls of the autopores and meso-
pores ; they have distinct cells, are devoid of tabule, and pro-
ject from the surface of the corallum in the form of blunt
spines. No mural perforations.
Type: Listulipora incrustans, Phillips, sp.
Fistulipora inerustans, Phill., sp.
Calamopora incrustans, Phillips, Geology of Yorkshire, part ii. p. 200,
pl. i. figs. 63, 64 (1836).
Berenicea megastoma, M‘Coy, Synopsis of the Carboniferous Fossils of
Treland, p. 195, pl. xxvi. fig. 18 (1844),
Fistulipora minor, M‘Coy, Ann. & Mag. Nat. Hist. ser. 2, vol. iii. p. 180
(1849); id. Brit. Pal. Foss. p. 79 (1851).
Ceramopora megastoma, Vine, Quart. Journ. Geol. Soc. vol. xxxvi.
p. 39, pl. xiii. (1880).
Ceramopora (Berenicea) megastoma, John Young, Ann. & Mag. Nat.
Hist. ser. 5, vol. x. p. 427 (1882).
[Non Fistulipora minor, Nich. Pal. Tabulate Corals, p. 306 (1879).]
Spec. char. Corallum incrusting, growing upon the stems
of Crinoids or other foreign bodies, and in the initial stages
of growth taking the form of small circumscribed patches,
often of a circular form. Adult crusts usually from 1 to 2
millimetres or more in thickness, the corallites being often more
or less reclined in the young crusts, but becoming erect in old
examples. ‘The mode of growth is from definite centres
(primitively one), from which the corallites radiate, and which
ultimately constitute so many stellate “macule.” The auto-
pores average $ millim. in diameter, and are slightly but quite
distinctly trifoliate in section. ‘The apertures in well-pre-
served specimens show very clearly the arched lip, which
depends upon the trifoliate form of the tubes. About three
autopores occupy a space of 13 millim. (=to about fifty auto-
* See note p. 516.
the Genus Fistulipora, I‘ Coy. 501
pores in an inch). Acanthopores are wanting. The auto-
pores are intersected by comparatively remote complete
tabule. The mesopores are crossed by more closely-set tabule,
Fistulipora incrustans, Phill, sp. A. Fragment of the corallum of the
natural size. B. Section of the same, to show vertical thickness,
C. Portion of surface, showing the autopores with their raised lips,
and the mesopores occupying the intervening spaces, enlarged about
twenty times. D. Transverse section, similarly enlarged, showing
fission in some of the mesopores. HE. Longitudinal section, similarly
enlarged: a, autopores ; m, mesopores ; ¢, primary cells.
which, owing to the incomplete nature of the walls of the
mesopores, often give rise to a sort of vesicular tissue. ‘The
““ macule ’’ are composed wholly of mesopores.
Obs. As regards the synonymy of this species, we have ex-
amined the original specimen of the Calamopora incrustans of
Phillips, from the Carboniferous Limestone, now preserved in
the British Museum, and we are satisfied as to its identity
with the Northumbrian and Scotch examples of Mistulipora
502. +Dr. H. A. Nicholson and Mr. A. H. Foord on
minor, M‘Coy, the originals of which were also obtained from ~
the Carboniferous Limestone. Phillips’s specimen of F. in-.
crustans is not well preserved, especially as regards its external '
surface; but we are not able to see in thin sections of it any
characters which would in any way separate it from 7. minor,
M‘Coy. Under these circumstances the species must stand as
Fistulipora incrustans, Phill., sp., and M‘Coy’s name must
hence be regarded as a synonym.
As to the propriety of ranking the fossil which M‘Coy
described (loc. cit.) under the name of Berenicea megastoma,
as also a synonym of Mstulipora incrustans, we cannot speak
with the same certainty, since we have had no opportunity of
examining M‘Coy’s original specimen. There can, however,
be no doubt that the fossil which has usually been identified
(notably by Mr. Vine and Mr. John Young) with Berenicea
megastoma, M‘Coy, is truly the young stage of Mistulipora
incrustans. Mr. John Young (loc. cit.) has fully demonstrated
this point. Whether, however, the fossil usually identified
with Berenicea megastoma, M‘Coy, is really the fossil so
named by M‘Coy is a point which could only be positively
decided by an examination of M‘Coy’s original example.
We are, however, disposed to believe that the identification is
correct, and we therefore place Berenicea megastoma, M‘Coy,
as a synonym of ff. incrustans, Phill.
On the other hand, the Carboniferous coral described by
one of us (Nicholson, Pal. Tab. Corals) under the name of
Fistulipora minor, M‘Coy, appears to be a distinct but closely-
related species, to which we shall here give the name of
F. muscosa. It does not differ essentially, however, from
typical examples of J. incrustans, Phill. (=F. minor, M‘Coy),
in anything except the rather smaller dimensions of the auto-
pores and the proportion which these bear to the mesopores.
The most distinctive characters of the minute structure of
F. incrustans are the comparatively large size of the auto-
pores and their being usually separated by no more than one
or two rows of mesopores. ‘The general shape of the auto-
pores is oval or circular, and the trifoliate form of the tubes in
cross section is not nearly so marked as it is in many species
of Fistulipora, though it is quite commonly recognizable.
That the autopores really have the form characteristic of the
genus is shown not only by tangential sections, but also by an
examination of the actual surface, many examples showing the
peculiar arching of one side of the aperture of the autopores
which is associated with this peculiar type of corallites.
F. incrustans shows clearly, as does its near ally F. muscosa,
the interesting phenomenon of the increase of the mesopores
the Genus Vistulipora, MZ‘ Coy. 503
by fission. In tangential sections the mesopores often exhibit
aseptum-like process extending to a greater or less distance
into the cavity of the tube. This phenomenon, so well known
as occurring in the genus Chetetes, Fischer, is the result of
the fissiparous development of the corallites. We have ob-
served precisely similar phenomena in the mesopores of
Constellaria antheloidea, Hall, and in the autopores of Mono-
irypa pulchella, KH. & H. In our opinion this fissiparous
mode of development is a strong argument in favour of the
reference of these forms to the Actinozoa rather than to the
Polyzoa.
In the earliest stages of growth Ff. cncrustans forms thin
subcireular crusts upon foreign bodies, each crust commencing
with a single ‘‘ macula,” from which the corallites radiate.
In the progress of growth fresh ‘ macule”’ are formed, and
the crust gradually spreads over the invested body. In older
colonies the original crust becomes thicker by the gradual
elongation of the corallites in a direction at right angles to the
invested surface. Sometimes also there may be a temporary
cessation of growth, and then a second layer of corallites is
formed above the old one. At the point where the corallites
are attached to the body which the colony invests they are
slightly bent, in a fashion which occurs in all the Monticuli-
poridee as also in all the Favositide, where the colony springs
from an extended surface, whether this surface belong to an
invested foreign body or whether it be the natural epitheca.
The obliquity of the young corallites thus produced is ren-
dered in F. ¢ncrustans apparently greater than it really is,
owing to the arching of the lips of the aperture of the auto-
pores on one side. As growth proceeds the corallites become,
however, quite erect. ven in the youngest colonies the
existence of both the autopores and the intervening meso-
pores may be recognized quite clearly. Nor is there any
difference whatever in the internal structure of young and old
colonies ; the only distinction, in fact, between the earlier and
the later stages being merely the slight obliquity of the coral-
lites of the former.
There seems to be little doubt that the fossil which M‘Coy
described (loc. cet.) under the name of Berenicea megastoma
was really a specimen of the young stage of Fistulipora
incrustans. As before remarked, however, it is not possible
to be absolutely certain of this without an examination of
M‘Coy’s original specimen, especially as M*Coy’s figure of
Berenicea megastoma does not exhibit any mesopores, nor does
his description of the species contain any allusion to the
presence ot “ interstitial tubes.”
504 Dr. H. A. Nicholson and Mr. A. H. Foord on
Mr. John Young, in the paper previously cited, not only
pointed out that the so-called Berenicea megastoma of M‘Coy
is really the young of Mstulipora minor, M‘Coy, but also
accepted Mr. Vine’s reference of the fossil to the genus Cera-
mopora, Hall. In this we are unable to agree with
Mr. Young, and we may briefly state the reasons which, in
our opinion, render inadmissible the course he has adopted.
In the first place, supposing it to be proved that the genera
named respectively F%stulipora and Ceramopora by their
founders were synonymous, it would be the genus Pistulipora,
M‘Coy, which would have to be retained, and Ceramopora,
Hall,suppressed. This is a mere matter of priority, /stulepora,
M‘Coy, having been founded in 1849, whereas Ceramopora,
Hall, was not established until two years later (Pal. N. Y.
vol. 11. 1851). Even, therefore, if we were able to accept Mr.
Young’s views on this point, the species now under consider-
ation would still have to be placed under the generic title of
Fistulipora. In the second place, we are unable to feel any
certainty as to what the genus Ceramopora, Hall, really is
supposed to include. The most recent definition of this genus
is that given by Mr. E. O. Ulrich (“ American Pal. Bryozoa,”
Journ. Cin. Soc. Nat. Hist. no. 38, vol. v. 1882), who defines
the genus as including types with “angular” cells and oblique
apertures, either with no “ interstitial cells” or few, generally
with “mural pores” and “occasionally” with tabule*.
Now F. tncrustans, Phill., does not possess ‘ angular”
corallites, always has numerous mesopores (“interstitial
tubes”), unquestionably has no mural pores, and always
possesses a larger or smaller number of tabule. It is there-
fore quite clear that F. incrustans cannot be placed under
Ceramopora, Hall, as this genus is understood by Mr. Ulrich.
It is also clear from Hall’s figures and description of the type
species of his genus Ceramopora (viz. C. imbricata, Hall),
that, whatever may be the precise structure of this form, it
has nothing in common with the coral here in question.
It need only be added that, supposing it had been shown
that the young stages of Mistulipora incrustans, Phill., were
identical in appearance with a presumed Polyzoan genus such
* The genus Ceramopora, as defined by Ulrich, can hardly be regarded
as a natural group, seeing that it is said to comprise forms with or with-
out “ interstitial tubes,” with or without mural pores (‘ connecting fora-
mina”), with or without tabula (“diaphragms”). The only character
as to which no option is given is that the apertures of the tubes are
oblique, wilh an arched “lip.” This character is, however, the principal
one given in the diagnosis of the family Ceramoporidsw, Ulrich, and it
cannot therefore be also used as a generic character of Ceramopora.
the Genus Fistulipora, M‘ Coy. 505
as Ceramopora, Hall, we should not for that reason adjudge
the evidence as to its zoological position derived from its
adult characters to be in any way invalidated. All that we
should feel inclined to say would be that, in the case sup-
posed, Mistulipora incrustans passed through a “ Ceramo-
poroid stage” or a ‘ Polyzoan stage,” in precisely the same
way that a Brachiopod may pass through an Annelidan stage
in its development, and yet may not become an Annelid.
As a matter of fact, however, we do not admit that Fistu-
lipora incrustans was at any period of its growth a Ceramo-
pora, or, indeed, in any way essentially different from what it
became when fully matured. On the contrary, thin sections
of the youngest specimens which we have been able to
examine show an internal structure in all respects precisely
similar to that exhibited by adult specimens. All that we
can admit is that in its early condition of a very thin invest-
ing crust Mistulipora incrustans may have the general aspect
of a Polyzoan; but here the resemblance ceases, and its inti-
mate structure shows no indication of any alliance with the
Polyzoa.
We think that from the evidence we have brought forward
there is now good ground for assigning to the genus Mistu-
lipora, M‘Coy, a place among the Actinozoa, and probably in
that division of it known as the Alcyonaria.
Formation and Locality. Fistulipora incrustans, Phill., is
found in the Carboniferous Limestone, Bolland, Yorkshire
(Phillips) ; Derbyshire and Ireland (J/*Coy). Also in the
Carboniferous rocks of Redesdale, Northumberland, where it
is common, and in the west of Scotland (John Young).
Fistulipora muscosa, Nich. & Foord.
(Pl. XV. figs. 3, 3 a.)
Fistulipora minor, Nicholson, Pal. Tab. Corals, p. 306,’ fig. 89 (1879)
[non Fistulipora minor, M‘Coy j.
Spec. char. Corallum forming thin irregular crusts, more
or less extensively attached to foreign bodies. Autopores
in the main oval, but commonly showing the trifoliate form
characteristic of the genus. ‘The autopores are rather less
than half a millim. in diameter, about three of them occupying
a space of 2 millim. (=about thirty-six in the space of an
inch). ‘The mesopores are angular and of variable size, two
rows usually intervening between any given pair of autopores.
The walls of the mesopores are very incompletely developed,
and the close-set tabule coalesce to form a vesicular tissue.
506 Dr. H. A. Nicholson and Mr. A. H. Foord on
The autopores have a few remote tabule, which in some tubes.
are seemingly altogether absent.
This species was originally described by one of us as Fistu-
lipora minor, M‘Coy (loc. cit.). In point of fact it is very
closely allied to this species (7. e. to F. incrustans, Phill.),
and differs from it only in certain minute characters. The
principal points which distinguish /. muscosa from F. ¢nerus-
tans are the slightly smaller size of the autopores and their
separation from one another to a proportionately greater dis-.
tance than in the latter species, this last feature depending
upon the more extensive development of the mesopores.
Moreover the mesopores of /. muscosa are furnished with
more imperfect walls than those of /. ¢nerustans, while the
autopores of the former are much more sparsely tabulate than
is the case in the latter.
Formation and Locality. Rare in the Lower Carboniferous
Limestone, Courland, near Kdinburgh (collected by Dr. Ram-
say H. Traquair).
Fistulipora crassa, Lonsdale, sp. (Pl. XV. fig. 1.)
Heteropora crassa, Lonsdale, Sil. Syst. pl. xv. figs. 14, 14 a (1839).
Fistulipora crassa, Nicholson, Ann. & Mag. Nat. Hist. ser. 5, vol. xiii.
p- 118, pl. vii. figs. 1, la, 2,2a@ (1884). [Non Fistulipora crassa,
Rominger, Proc. Acad. Nat. Sci. Phil. p. 121 (1866).] -
The fine specimen we have figured is from the collection of
the late Mr. Johnson, of Dudley. Whe species has already
been described and its microscopic structure illustrated by one
of the writers in this journal (doc. cit.). ‘The small dark spots
upon the surface of the specimen represent the “ macule.”
The name of Dr. Rominger’s species (doc. czt.) must now be
changed, and we propose for it that of /istulipora Romingert.
F. crassa is not uncommon in the Wenlock Shales at
Dudley, and it is found also at Benthall Edge and at Dor-
mington.
Fistulipora nummulina, Nich. & Foord.
(Pl. XV. figs. 2-2 c.)
Spec. char. Corallum discoid, lenticular, concavo- or plano-
convex, also forming thin, irregular, crust-like expansions;
sometimes the corallum rises into a conical mass, with tapering
margins, the central portion thus attaining a thickness greatly
disproportionate to that of the margins. ‘The surface is dotted
over with numerous “ monticules”’ (consisting of mesopores),
which are slightly raised above the general level; they were
doubtless more elevated originally, but have been reduced in
height by the attrition which the whole of the corallum has
the Genus Fistulipora, M‘ Coy. 507
undergone. The autopores are sufficiently large to be distinctly
seen with the naked eye; this arises in some measure from
their infilling being of a
lighter colour than that of the Fig 4.
walls of the cells, otherwise
they could hardly be perceived.
They are oval or subcircular in
form, the folds (which are plainly
visible under a 1-inch objective)
occupying. about one fourth of
the circumference of the walls
and always pointing towards
one of the centres of growth.
About four of the autopores may
be contained within the space of
1 millim. ; a few of a somewhat
larger size are grouped around
the ‘‘ monticules.” | Mesopores
as seen in transverse section
poly gonal, wey variable MM SIZe, F. nummulina, showing folds in
sometimes equalling that of the the autopores.
autopores, sometimes much
smaller. Longitudinal sections show that the autopores are
provided with tabule, which are horizontal or a little curved,
and that the mesopores are filled with closely-set tabule
which have produced by their coalescence a vesicular tissue.
Obs. The species to which F. nummulina is most closely
allied is undoubtedly £. crassa. Externally the distinction
between the two is very obvious, as appears on looking at the
figures (Pl. XV. figs. 1,2), one being of a discoid or flattened
shape, and the other branching. In their microscopic charac-
ters also the two species are distinct enough ; the autopores in
F. nummulina being larger than those of F. crassa, only four
of them being required to fill the space of a millimetre in the
former species, while in the latter five must be taken.
Further, the tabulation of the mesopores is not nearly so
dense in /. nummulina as it is in F. crassa, and its vesicular
character is therefore not so strongly marked as it is in that
species.
The present species is not unfrequently met with in the
grey and greenish shales of the Wenlock group. The speci-
men figured was presented to one of the writers by Mr. W.
Madeley, of Dudley, who has for many years collected the
fossils of that region with much industry and discrimination.
Other specimens referred to in drawing up the foregoing de-
scription are from the cabinet of Mr. C. Holcroft, also of
Dudley.
508 Dr. H. A. Nicholson and Mr. A. H. Foord on
Fistulipora utriculus, Rominger.
(Pl. XVI. figs. 1-le, & Pl. XVII. figs. 1, 1 a.)
Fistulipora utriculus, Rominger, Proc. Acad. Nat. Sci. Phil. p. 121
(1866) [no figures].
Corallum small, irregular, subramose, hollow, thin, sub-
cylindrical or compressed; varying from 4 millim. to 1
millim. or rather more in thickness. The surface is covered
with monticules, which take the form of warty outgrowths,
whose summits consist of clusters of mesopores. The latter
may be seen with a strong hand-lens.
Under the microscope the surface of the corallum is observed
to be minutely granulose (Pl. XVI. fig. 1 4), the granules being
apparently the free ends or summits of the walls of the meso-
pores. The autopores can generally be seen without a lens;
about four of them fill the space of 1 millim., and, as appears
to be always the case, some of slightly larger size occur in
the region of the ‘‘monticules”’ or areas of growth. ‘The
mesopores are of the usual angular form. The folds of the
autopores are in this species remarkably well developed ; they
oceupy from one third to one fourth of the circumference of the
apertures; the latter are surrounded by a shallow depression,
and their margins are slightly exsert. The outlines of the
walls of the mesopores can be very distinctly made out in
weathered specimens (Pl. XVII. fig. 1).
In tangential sections the autopores are seen to be of an
irregular oval shape and of variable dimensions; the meso-
pores are sufficiently abundant to make three or four rows
around the autopores. ‘The areas of growth, as already stated,
are found to be occupied entirely by the mesopores, and around
them the autopores are ranked in three or four concentric rows
(Pl. XVI. fig. 1c). Longitudinal sections show that the
autopores have but few tabulee, while those of the mesopores
are abundant and are of the usual vesicular description.
Obs. We give some additional figures of this very charac-
teristic and interesting species. Fig. 1, Pl. XVII., is a micro-
scopic view of the slightly weathered surface. It is drawn on
the same scale as fig. 16, Pl. XVI.* (enlarged about forty
times), and shows the walls of the mesopores ; the interior of
these cells, as well as that of the autopores, being filled with
crystalline calcite. Fig. 1a, Pl. XVIL., is intended to illustrate
the projection of the autopores above the general surface of the
corallum and the prominence of the arched lips (folds).
Dr. Rominger (/oc. czt.) has compared this species with two
* In this figure the walls of the mesopores are not indicated, because
they are not visible in this part of the specimen, owing, it would seem, to
their uniformity of colour with the rest of the surface.
the Genus Fistulipora, M‘ Coy. 509
others described by him, viz. /. ertensis and F. spinulifera.
We cannot corroborate the accuracy of his comparison with
reference to the latter of these forms, for we do not possess
specimens of it; but with regard to F. ertensis we find
ourselves quite unable to agree with Dr. Rominger. It is in
every way a coarser form than J. wériculus; it occurs in
large laminate folded masses, and the autopores greatly ex-
ceed in magnitude those of /. utriculus. F. eriensis, more-
over, is provided with acanthopores, which are wanting in
F, utriculus.
The present species resembles Fistulipora trifoliata, Schliit.
(Pl. XVIII. figs. 1-1), in the strong development of the
folds of the autopores, but in other details of its structure as
well as in its habit of growth it is sharply distinct from that
form. There is another species, however, to which Pistuli-
pora utriculus is very closely related, viz. /. Goldfussi; and
it was not without hesitation that we resolved to keep them
apart. Both are exactly similar in habit of growth and ex-
ternal markings, and there is also a general conformity in
their minute structure. The points in which the two species
are dissimilar are these: the autopores are larger and less
numerous in F. wériculus than they are in Ff. Gioldfussi, and
the folds are more strongly developed in the former species
than they are in the latter.
Formation and Locality. Common in the shales of the
Hamilton group (Devonian), at Thetford (formerly called
Widder), and at Arkona, in the Province of Ontario, Canada.
Fistulipora Torrubie, De Verneuil & Haime, sp,
(PIS DOVI es) 25)2 a, 210.)
Chetetes Torrubie, De Verneuil & J. Haime, Bull. Soc. Géol. de France,
Qe sér. t. vil. p. 162 (1850) [mo description or figures}; Milne-
Edwards & Haime, Polyp. Foss. des Terr. Pal. p. 268, pl. xx.
figs. 5, 5 a (1851).
Monticulipora Torrubie, Milne-Edwards, Hist. Nat. des Coralliaires,
tom. iii, p. 277 (1860).
Spec. char. Corallum subramose, or in large sublobate
masses, which present a coarsely mamillated appearance
and are made up of a succession of concentric superimposed
lamine. Surface monticulose; the monticules rather incon-
spicuous, distant from each other 3 or 4 millim. Autopores
subcireular or oval in general outline, closely approximated ;
rarely in contact; readily distinguishable by the naked eye.
About three of those of average size occupy the space of
1 millim., and about two of the larger ones, which are in the
region of the “‘ monticules,” filla similar space. The folds of
510 Dr. H. A. Nicholson and Mr. A. H. Foord on
the autopores may be seen on well-preserved surfaces under the
microscope; they are small, occupying not more than about
one sixth of the circumference of the walls. A few autopores
have been drawn on an enlarged scale (Pl. XVI. fig. 2a) to
show the folds. The latter become very obscure in sections
cut below the surface layers of the corallum, and they were
overlcoked in the larger section (fig. 2). The autopores, as
shown in longitudinal sections (fig. 2 6), are crossed by tabule,
which are comparatively numerous, and are separated from each
other by variable spaces, measuring roughly from one to two
tube diameters. ‘The mesopores are in this species remarkably
few in number, so that it frequently happens that only a single
row of them is interposed between two of the autopores. The
tabulee in the mesopores are unusually wide apart, and some-
times occur at the same level in contiguous tubes, which appear
at first sight to be separated by distinct walls. In other parts
of the corallum, however, the characteristic vesicular tabule
are met with.
Obs. This species was first described and figured in the
‘ Polypiers Fossiles des Terrains Paléozoiques’ (loc. cit.).
The first notice of it, however, appeared in a list of Devonian
fossils from the district of Sabero (Léon) by M. de Ver-
neuil (loc. cét.). The description of Fistulipora Torrubie by
the authors of the ‘ Polypiers Fossiles’ refers only to its
external characters.
The species to which this is most nearly allied is /%stulz-
pora incrassata, Nich. (Pal. Tab. Corals, p. 308, pl. xv.
figs. 83-3 6, 1879), from the Hamilton group (Devonian) of
Canada. The corallites in that species are, however, some-
what larger than those of &. Torrubie, the mesopores less
numerous, aud the folds of the autopores more strongly
developed.
formation and Locality. F. Torrubie is somewhat widely
distributed geographically, and is reported to have been found
in Devonian rocks at the following localities :--Asturias
(Spain), Eifel (Westphalia), Boulonnais &c. (France).
Fistulipora Goldfussi, Michelin, sp.
(Pl. XVII. figs. 2, 2 a, 2 6.)
Ceriopora Goldfussi, Michelin, Iconogr. Zoophyt. p. 190, pl. xlviii.
fig. 9 (1847).
2 Chicstetes Goldfussi, Quenstedt, Petref. Deutsch]. Abtheil. i. p. 83,
t. exlvi. figs. 28, 29 (1878).
Corallum ramose, hollow, subcylindrical. Surface uneven,
irregularly dilated here and there. “ Macule” not ver y cou-
spicuous. Corallites very minute ; about seven of the autopores
the Genus Fistulipora, M‘ Coy. 511
may be contained within the space of 1 millim. The folds
occupy from one fourth to one fifth of the circumference of the
autopores. -
Obs. The relationship between Pstulipora utriculus and
this species has already been pointed out.
We are indebted to Dr. Henry Woodward, F.R.S., for his
kindness in permitting us the use of specimens contained in
the collections of the British Museum (Nat. Hist.) in pre-
paring the foregoing description.
Fistulipora dobunica *, Nich. & Foord.
(Pl. XVII. figs. 8, 3 a, 36.)
Corallum extremely thin, incrusting; attaching itself to
various foreign bodies, whose surface contour it follows in all
its irregularities ; occasionally, however, putting forth short
hollow cylindrical prolongations, generally at right angles to
the surface (fig. 3). Surface dotted with macule. The
corallites, though very minute, can usually be seen by the
naked eye. About six of the autopores are contained within
the space of 1 millim.; others, of a little larger size, occur in
the vicinity of the macule. ‘The folds in the autopores are
well developed and occupy nearly one third of the circum-
ference of the walls of those corallites (fig. 3a). There is
nothing remarkable in the microscopic structure as seen in
longitudinal sections.
Obs. As might be supposed, some difficulty was experi-
enced in obtaining satisfactory sections from such an extremely
thin corallum.
Some of the autopores have been shaded, the better to
distinguish them from the mesopores.
We are unacquainted with any species with which to com-
pare #, dobunica. The extreme tenuity of its corallum and
its incrusting habit resulting from this, together with the
minuteness of its corallites, are the distinguishing marks of
this species. The specimen figured is from the collection of
Mr. Madeley, of Dudley.
Formation and Locality. F. dobunica appears to be tolerably
plentiful in the Wenlock Shales (Upper Silurian) at Dudley.
Fistulipora ertensis, Rominger. (Pl. XVII. figs. 4, 4a.)
Fistulipora eriensis, Rominger, Proc. Acad. Nat. Sci. Phil. p. 121
(1866).
Corallum in large, irregular, laminated and folded masses ;
* The Dobunii were a tribe of. ancient Britons, neighbours of the
Silures.
512 Dr. H. A. Nicholson and Mr. A. H. Foord on
growing in concentric layers measuring as much as 8 centim.
in breadth and 2 centim. in thickness. Surface monticulose ;
the monticules conspicuous, from 2 to 3 millim. apart, con-
sisting of mesopores. Autopores comparatively large, readily
distinguishable by the naked eye. About three of them fill
the space of 1 millim. The folds are of average size and
occupy about one fourth of the circumference of the walls of
the autopores. Acanthopores may be seen in transverse sec-
tions at the angles of the walls of the mesopores. Longitu-
dinal sections show considerable regularity in the disposition
of the vesicular tabule in the mesopores. The autopores
have very few tabule.
Obs. The presence of acanthopores distinguishes Fistu-
lipora eriensis from all other species of the genus with the
exception of I”. ludensis, Nich. (this journal, *p. 119, Feb.
1884), from which it is completely separated by its habit of
growth and the much larger dimensions of its corallites. The
occurrence of acanthopores is in fact the only feature which
these two species possess in common. The expression ‘ spi-
nuloso-granulose,’’ employed by Dr. Rominger in reference
to the surface of this species, no doubt refers to the acantho-
pores, which may be visible externally on well-preserved
specimens. We have only detected them in transverse
sections.
Formation and Locality. Hamilton Group (Devonian),
Canandaigua, Ontario Co., New York.
Fistulipora etfeliensis, Schiliiter, sp.
Callopora etfeliensis, Schliit. Sitzungsberichte der niederrheinischen
Gesellschaft in Bonn (Physikalische Section), p. 72, Feb. 14, 1881.
Corallum hemispherical, with aslightly conical base, which
may have been furnished with an epitheca. The surface is
provided with slightly raised “ monticules,”’ upon which
there are clusters of the mesopores. In weathered specimens
the corallites may be very distinctly made out; they
measure about 14 millim. in their longer diameter by about
1 millim. in their shorter. The autopores are irregularly oval
or subcircular in outline, and are in general completely iso-
lated from each other by the mesopores, but occasionally two
come into contact either at their sides or at their extremities.
The folds are very small in this species, as may be seen in
the section, fig. B. The mesopores vary greatly both in size
and in shape; in some instances four of them encircle an
autopore, in others six.
Longitudinal sections show that the autopores are divided
the Genus Fistulipora, MM‘ Coy. 513
by a few remote tabule, while the mesopores exhibit the cha-
racteristic vesicular tabulation of the genus, especially near
the base of the colony. As growth proceeds this tabulation
assumes amore regular appearance, and may consist of two
or more rows of cells as it were dovetailed into each other
(fig. 5, D).
Fig. 5,
Fistulipora etfeliensis, Schlut. sp. A. Corallum, natural size; the shading
is given merely to show the rotundity of the specimen and the some-
what conical base. B. Transverse section, enlarged about twelve
times. C. One of the autopores, showing the fold, enlarged about
twenty times. D. Longitudinal section, enlarged about twelve
times. a, autopores ; m, mesopores.
Obs. An interesting feature is noticeable in the mesopores
of this species. Certain of them, larger than the average
and of a subelliptical form, are partially divided by a pro-
jection as thick as the cell-walls, which extends from those —
walls about halfway across the cell-cavity (woodcut, fig. 6).
Ann. & Mag. N, Hist. Ser. 5, Vol. xvi. 35
514 Dr. H. A. Nicholson and Mr. A. H. Foord on
These projections appear to indicate very clearly a fissi-
parous mode of growth in such cells.
In drawing attention to the sub-
stitution of the generic name Fstu- Fig. 6.
lipora for that of Callopora, to .
which latter genus Prof. Schliiter
assigned the present species, we
have only to observe that there
exists a well-marked distinction
between the two genera, which
may be briefly stated as follows :—
In Fistulipora, as has been shown
above, the mesopores are crossed
by imperfect tabulee, which, coales-
cing, form a vesicular tissue; in
Callopora, on the other hand, the
tabulation of the mesopores is not
essentially different from that of 4g, autopore; m, mesopore ;
the autopores, except that the f, fission.
tabule are much more numerous in
the former cells than they are in the
latter. The mesopores in Callopora are further, as a rule,
bounded by perfect walls. It is scarcely necessary to point
out that the structure of the present form accords with that
of Histulipora and not with that of Callopora.
Fistulipora eifeliensis stands alone in the remarkably large
size of its corallites, which exceed in their dimensions those of
any other species of /%stul‘pora with which we are acquainted.
formation and Locality. Not uncommon in the Middle
Devonian of Gees, near Gerolstein, Hifel.
Fistulipora trifoliata, Schliter. (Pl. XVIII. figs. 1-1 ¢.)
Fistulipora trifolhiata, Schliit. Sitzungsberichte der niederrheinischen
Gesellschaft in Bonn (Naturwissenschaftliche Section), p. 147,
May 11, 1885.
Corallum hemispherical, growing on the shells of mollusks
and other foreign objects. Surface not well preserved in any
of the specimens examined, apparently smooth. Corallites
extremely minute, barely distinguishable by the naked eye.
““Macule” distant from each other from 8 to 4 millim.
About six of the autopores fill the space of 1 millim., while
some of a larger size invest the “ macule.” On looking at a
tangential section (figs. 1 a, 16) it is found that the autopores
have their outline interrupted by the very strong folds in their
walls, which impart a distinctly trifoliate aspect to them.
The free edges of the folds sometimes extend far into the lumen
the Genus Fistulipora, Mf Coy: 515
of the cells. The mesopores are sufficiently numerous to
completely isolate the autopores from each other; they exhibit
the usual polygonal form. A few, of a comparatively large
size, occupy the central portions of the ‘‘ maculz,” and towards
these the folds of the autopores are directed. Longitudinal
sections show the finely vesicular character of the tabule in
the mesopores and the growth of the corallum in concentric
layers. ‘These sections also show that the autopores diverge
in a flabellate manner from their centres of growth. A like
feature is also noticeable in F’. cornavica (Pl. XVIII. fig. 2 ¢).
Obs. The present form has been well known to us for more
than a year, but we have not till now been in a position to
publish a description of it. In the meantime Professor
Schliiter, of Bonn, has been before us in the matter. As,
however, that author has given neither figures nor measure-
ments of his species, we have felt ourselves justified in re-
describing it and supplying those deficiencies, more especially
as it exhibits in amarked degree one of the most characteristic
features of the genus, viz. those remarkable folds in the walls
of the autopores.
In its general structural features this species resembles
F. cornavica, Nich. & Foord (énfra). The two species are
figured upon the same Plate (X VIII.) to facilitate comparison.
It will be seen that the corallites of F. cornavica are larger
than those of F. trifoliata, and also that the autopores in the
latter are more highly developed than they are in the former.
We are indebted to Prof. Schliiter for sections of J tri-
foliata, which place beyond question the specific identity of
his species with ours, a point which we were unable to decide
from his description alone.
Formation and Locality. Somewhat rare in the Middle
Devonian of Gees, near Gerolstein, Hifel.
Fistulipora cornavica*, Nich & Foord.
(Pl. XVIII. figs. 2-2 ¢.)
Corallum subhemispherical, attached by its base to shells
or other marine objects; composed of a succession of thin
concentric layers, which apparently mark periodical cessa-
tions of growth. Surface monticulose, the ‘ monticules ”
consisting of mesopores. Autopores, as seen in transverse
sections, irregularly ovate, the folds occupying about one
fourth of the circumference of their walls. About four of the
autopores fill the space of 1 millim. Mesopores nume-
* The Cornayii were a tribe of ancient Britons who, along with the
Ordovices, inhabited Shropshire at the time of the Roman invasion.
30%
516 On the Genus Fistulipora, M‘ Coy.
rous and mostly of large size. Longitudinal sections show
that the tabule by which the cavities of the autopores are
crossed are placed at irregular distances apart. The diver-
gence of the autopores from their centres of growth may also
be observed in these sections (fig. 2 ¢).
Obs. A comparison has already been made between this
form and F, trifoliata in treating of the latter.
Formation and Locality. Appears to be rare in the Wen-
lock Shales (Upper Silurian) at Buildwas, Shropshire.
Notr.—In his Hist. Nat. des Coralliaires (vol. 1. p. 67,
1860) M. Milne-Edwards gives a highly suggestive explana-
tion of what he conceives to have been the origin of vesicular
tabule. We beg permission to lay before the reader the
following translation of it :—
“According to the known disposition of the soft parts of
the polyps it is evident that the tabule should correspond to
the spaces left open by the atrophy or the successive retreating
of the inferior extremities of the mesenteric folds [dames], and
the degree of their separation would depend upon the length
to which this retreating or atrophy was carried in proportion
to the growth of the animal. If this upward movement [of
the animal] was effected rapidly and completely in each cell
[Coge] it would result in the tabule being simple and apart
trom each other. But if the movement was made little by
little in an incomplete and limited manner in the different
parts of the cells there would be formed a series of blisters or
vesicles, of which the general appearance would be that of a
cellular or vesicular tissue.”
EXPLANATION OF THE PLATES.
PLATE XV.
Fig. 1. Fistulipora crassa, Lonsd. sp. View of corallum in the matrix,
nat. size. (Coll. Johnson, Dudley.)
Fig. 2. Fistulipora nummulina, Nich. & Foord. View of upper surface
of corallum, nat. size.
Fig. 2.a. Side view of the same specimen, to show thickness of corallum.
Fig. 2b, Transverse section, enlarged about twenty times.
Fig. 2c. Longitudinal section, similarly enlarged.
Fig. 3. Fistulipora muscosa, Nich. & Foord. Transverse section, enlarged
about twenty times.
Fig. 3 a. Longitudinal section, enlarged to the same extent.
Pratr XVI.
Figs. 1, 1a. Fistulipora utriculus, Rom. Two examples of the corallum
of this species, nat. size.
Bibliographical Notice. 517
fg. 1b. Surtace, showing arched lips (folds) at the apertures of the
autopores, enlarged about forty times.
Fig. 1c. Transverse section, showing one of the ‘ macule,”’ with the
autopores ranged around it; enlarged about twenty times.
Fig. 1d. A portion of the same section, enlarged about forty times.
Fig. Le. Longitudinal section, enlarged about twenty times.
Fig. 2. Fistulipora Torrubie, De Vern. & Haime. Transverse section,
enlarged about twenty times.
4g. 2 a. Portion of another section, to show folds in the autopores, en-
larged about forty times.
Fig. 2 6. Longitudinal section, enlarged about forty times.
Priate XVII.
Fg. 1. Fistulipora utriculus, Rom. Surface partially weathered, showing
autopores and mesopores, enlarged about forty times.
F%g.1a. Surface of the same, viewed in profile, showing prominence of
the arched lips of the autopores. Similarly enlarged.
Fig. 2. Fistulipora Goldfussi, Mich. Corallum of the natural size.
Fig. 2 a. Transverse section, enlarged about twenty times.
£g. 2b. Longitudinal section, enlarged to the same extent.
Fig. 5. Fustulipora dobunica, Nich. & Foord. View of the corallum of
the natural size.
Fig. 3 a. Transverse section, enlarged about twenty times.
Fig. 36, Longitudinal section, similarly enlarged.
Fig. 4, Fistulipora eriensis, Rom, Transverse section, enlarged about
twenty times.
Fig. 4a, Longitudinal section, similarly enlarged.
.PuaTE XVIII.
Fig. 1. Fistulipora trifolkiata, Schlut. View of the corallum of the natural
size,
Fig. 1a. Transverse section of one of the “macule,”’ enlarged about
twenty times.
fig. 16. Transverse section, enlarged about forty times.
Fg. 1c. Longitudinal section, enlarged about twenty times.
tg. 2. Fistulipora cornavica, Nich. & Foord. View of the corallum,
growing on a Brachiopod shell. Nat. size.
Fig. 2 a. Transverse section, enlarged about twenty times,
Fxg. 2b. One of the autopores, enlarged about forty times.
Fig. 2c. Longitudinal section, enlarged about twenty times.
BIBLIOGRAPHICAL NOTICE.
Contributions to the Knowledge of the Older Mesozoic Flora of
Virgoua. By Witt1am Morris Fonrainr. Monographs of the
United States Geological Survey. Vol. VI. Pp. 144, with 54
plates. Washington: 1883.
Tur present volume contains a very full account of the older Meso-
zoic flora of Virginia. The author introduces the subject by a short
geological sketch of the area from which the fossil plants were
collected, in which is pointed out that the Mesozoic strata of Vir-
ginia are divisible into two well-marked groups, an older and a
younger, both of which are characterized by plants of a totally _
different aspect. It is only those from the older Mesozoic group,
however, with which the present monograph deals.
518 Bibliographical Notice.
By far the greater portion of the specimens described in the work
were derived from the area in the neighbourhood of Richmond
which Mr. Fontaine distinguishes as the “ Richmond Coal-field,”
as it is the most important district and eontains nearly all the
workable coal in the Mesozoie strata of Virginia. Considerable
difficulty has been experienced in collecting specimens, as few
openings have been made in the strata for many years; hence the
specimens had in great measure to be collected from old and
weathered refuse-heaps. Thus the work of securing good examples
has been one of great labour.
As typical of the older Mesozoic areas of Virginia and as the most
completely explored, the geology of the Richmond Coal-field is more
fully described than that of any of the other areas. It contains
several valuable coal-seams, but their number and thickness vary
much in different parts of the field. There are, however, two im-
portant seams which appear to be persistent; of these the lower,
called the main or big seam, is the most valuable, and though varying
greatly in thickness and often dividing into two seams, attains at
Clover Hill a varying thickness of from 15 to 26 feet.
The second part of the work comprises the description of the
fossil plants, in which two new genera are created and many new
species described. One of the new genera is named Mertensides,
from the similarity of the individuals it embraces to the Mertensia
group of the Gleicheniaces ; but the ferns it includes differ in not
showing the characteristic dichotomy of the Mertensia. The type
of this genus is Mertensides (Pecopteris) bullatus, Bunbury,sp. ‘The
other new genus is Pseudodancopsis, containing ferns with a Dicty-
opteroid nervation, but which also in some of their characters
approach to Heer’s Dancopsis. It contains two species, Pseudo-
dancopsis reticulata and P. nervosa.
Among the new species, Lonchopteris virginiensis is of special
interest. The genus Lonchopteris was formerly regarded as Paleo-
zoic, and only known to occurin the Coal-measures ; but in Lon-
chopteris virginiensis there is one of the most handsome species of
the genus, which is now shown to extend upwards to the Rhetie.
In all forty-two species of plants are described from the older Meso-
zoic rocks of Virginia; of these, twenty-one are peculiar to the
locality, four are either found in the Trias or allied to Triassic forms,
eight are similar to plants found in the Jurassic or allied to plants
occurring in rocks of that age, and twelve are either found in the
Rheetic or allied to plants of that formation.
The third part of the work is devoted to the older Mesozoic
flora of North Carolina, with the object of instituting a comparison
between its fossil flora and that occurring in the Virginian Mesozoic
area. Many of Emmons’s species from North Carolina were, how-
ever, inaccurately determined; hence it wasnecessary for Mr. Fontaine .
to enter into a critical examination of Emmons’s species, and as far
as possible to correct his determinations. In the treatment of this
difficult pat of his subject Mr. Fontaine has acted most fairly, for
he gives in Emmons’s own words the descriptions of that writer’s
Miscellaneous. 519
species, accompanying them with a reproduction of the original
figures ; on these plants Mr. Fontaine makes many notes and cor-
rections.
With the list of North-Carolina plants thus corrected a compari-
son is made with those from Virginia, which shows that both areas
are of the same age.
A further comparison of the fossil plants from North Carolina
and Virginia is instituted with those from Indian and European
Mesozoic rocks, when the author arrives at the conclusion that the
Mesozoic floras of North Carolina and Virginia are most probably
Rheetic in age, certainly not older ; he is also inclined to regard the
Rheetic as forming transition beds, having more affinity with the
Lower Lias than with Triassic strata.
The whole work evinces very careful investigation ; the descrip-
tions are full and the value of the monograph is greatly enhanced
by the numerous figures which accompany the descriptions. The
book cannot fail to prove of the greatest value to those interested
in fossil botany. The author has contributed a valuable addition
to the ever-increasing monographs of the United-States Geological
Survey.
MISCELLANEOUS.
Instinct of Orientation im Helix aspersa. By F. p’A. Furtapo.
In a house which I inhabited at St. Michael’s, one of the Azores,
there was a veranda with a flight of steps leading to a little court
or garden. Above this was a second veranda supported by a stone
column, which rested on the wall of the lower veranda. At the
foot of the column had been set a flower-pot with a young banana
bearing two or three leaves.
One morning I noticed a snail (Helia aspersa) lodged between
the pot and the column, as if waiting for night to attack the plant.
A leaf had already been gnawed, and to stop further depredations I
threw the snail into the court. It was not much the worse for the
fall, as it chanced to light upon a small manure-heap.
Next morning I was surprised to find the snail in precisely the
same position as kefore between the pot and the column. I knew
it by its size and colour, as well as by a curious covering of spiders’
webs which it bore. It was evident that the snail possessed a
remarkable sense of direction, which enabled it, after a violent
shock, to make its way back over a distance of at least 6 metres in
a very short time. In order to get to the bottom of the matter I
threw the snail back to the heap and watched the result, which
was as follows :— :
June 10, 1884.—At about 9 a.m. the snail was resting, completely
retracted within its shell, on the rail of the staircase, having tra-
velled nearly 4 metres. In the evening it resumed its march, but
so slowly that by 10 o’clock it had only reached the top of the rail,
where it stopped again, haying traversed a metre in two hours.
520 Miscellaneous.
Twenty minutes after midnight it began to travel along the balus-
trade of the veranda, taking at first a very undecided course, but
as soon as it reached the edge of the balustrade making straight for
the banana. Halfway it was turned aside by some fish-scales,
which no doubt indicated that the surface was contaminated; but
it soon regained its previous direction. Near the column it fell in
with a grooved washing-board, which it seemed to remember, for it
reared its head and tentacles towards it while still 2 centimetres off.
So far 2 metres had been traversed in twenty minutes. The snail
now advanced resolutely from the board to the flower-pot as if over
known ground. (The board had lain in the same place for several
days.) I watched its movements by a lamp set far off so as to give
only a faint light; but when it reached the pot the animal became
shaded by weeds which grew there, and I found it necessary to
bring the lamp near, in order to observe the movements of the snail’s
lips and tentacles. It climbed the pot rapidly, mending its pace
as it got nearer, then it examined the rim with care, and at last
crawled over the mould. For a quarter of an hour it wandered
among the weeds in the pot, licking them frequently. When I saw
it explore the soil with its lips and larger tentacles, while the re-
productive orifice seemed to open from time to time, I thought that
it was seeking a convenient spot to lay its eggs. At last it came up
to the banana, mounted it, and began to gnaw the leaf previously
attacked exactly where it had left off before. I was standing a
little way off to avoid disturbing the snail, but could readily detect
the peculiar odour of the gnawed leaf. Very likely the snail could
perceive, even in an uninjured leaf, that scent which only became
apparent to me when the leaf was bruised or cut, and this may haye
helped to guide its course. Scent alone will not, however, explain
all the movements of the animal. At 2 p.m. I left it feeding.
June 11.—At 10 a.m. very little of the leaf had been devoured.
The snail was comfortably established, as before, between the column
and the pot.
After this the snail wandered over a vine which trailed about the
column and upper veranda. Finding that it was disposed to escape
to the next garden, I opened it on June 17 to see whether it was
ready to lay eggs. There was not a single egg in the oviduct, and
a large dart in the dart-sac proved that no sexual congress had
lately taken place.
These observations seem to show that a land-snail may possess an
instinct which enables it to choose its abode and return to it at
pleasure. We have here the same love of home and topographical
knowledge which have been observed, and noted with wonder, in
the limpet (George Roberts, in Woodward’s ‘ Manual of Mollusca,’
p- 11).—-Zoological Section of the Lisbon Museum, Oct. 27, 1885.
On the Ewistence of a Postoral Band of Cilia in Gasteropod Veligers.
By J. Puayrarr M‘Mourricu.
The question as to the phylogeny of the Mollusca is as yet unde-
cided, though recent researches indicate a relationship between this
group and that of the Annelida. The discovery of the peculiar
Miscellaneous. | 521
forms Neomenia, Proneomenia, and Chetederma gave a strong im-
pulse to this idea on account of their similarity in some respects to
what obtains in the Polyplacophora; but it is not safe to argue a
direct descent from these forms, or even to imagine that they come
into the ancestral line at all. It is quite possible that they and the
Polyplacophora are offshoots from the direct stem, and probably we
must look more to the embryological history of the Gasteropods for
light on the subject. Attempts have been made, notably by Hat-
schek (‘ Studien ti. Entwickelungsgesch. d. Anneliden,’ Wien, 1878),
to trace a relationship between the Polygordius-larva of the Anne-
lida and the Molluscan larva, and thus to throw any relationship
which may exist between the two groups back to a very early period
in their evolution.
If it can be shown that there is considerable similarity between
the larvee of the two groups, and if the differences which do exist
can be explained as adaptations to new conditions, the presumption
as to the genetic relations between the larve will be greatly
strengthened. As regards the arrangement of the cilia, which is
the only point to be dealt with in this note, we have in the Poly-
gordius-larva a strong preoral locomotive band, a more delicate
postoral nutritive band, and a still less apparent ciliated region lying
between these two bands and leading into the ciliated mouth. The
identity of the cilia of the velum of the Gasteropod larva with the
first of these has been frequently noticed ; they form a strong pre-
oral band, occasionally double, and differing from the band of the
Polygordius-larva only in the extent of its development, and in its
incomplete closure in many cases dorsally. This latter point of
difference does not, however, hold throughout; the former may be
explained by the necessity for a more powerful locomotive apparatus
than is required for the Annelida, caused by the presence of a shell,
a structure which appears very early in the life-history of the Mol-
lusca. A postoral band has never as yet been described for the
Prosobranchs. Several observers have called attention to the pre-
sence of a single band of cilia behind the cilia of the velum, and
have regarded it as nutritive in function, and the object of this note
is to call attention to the fact that this band passes across the ventral
surface of the larva behind the mouth, and is therefore quite com-
parable to the postoral band of the Trochophore. My attention was
first called to this fact in the larve of Crepidula fornicata, and I
was afterwards able to confirm it in those of Fulgar carica, in a
species of Weptunea, in two Prosobranch Veligers as yet undeter-
mined, and in the Opisthobranch Montaguia, sp.? In the undeter-
mined Veligers the velum was produced into four long flattened
arms, round the margins of which were the strong locomotor cilia.
On the under surface of the arms, running paralle! to and not very
remote from the locomotor cilia, was the finer band of nutritive
cilia, the transparency of the arms and their size rendering it very
apparent, and it could without much difficulty be traced across the
ventral surface of the body immediately behind the mouth. Dr. W.
K. Brooks informs me that he noticed the existence of this postoral
band some time ago, and was then inclined to attribute some phylo-
522 Miscellaneous.
genetic importance to it; but being occupied with other investiga-
tions he did not follow up his observations, and refrained from
publication. Haddon also has described and figured it for certain
Opisthobranchs, but does not seem to have observed it in the Proso-
‘branchs he studied.
The region between these two bands is occupied by numerous
very fine cilia, which, as in the Polygordius-larva, are continuous
with those lining the mouth-opening and the cesophagus. The ar-
rangement of cilia which is to be found in the typical Annelid larva
is therefore almost exactly reproduced in the Gasteropod Veliger.
Arguing from ontogeny, a phylogenetic history of the Gastero-
pods somewhat as follows may be constructed. They and the
Annelida have had their origin in a Trochophore. In the Gastero-
pods this ancestor developed a univalve shell, represented by the
larval shell so often replaced as development proceeds by another
more ornamented and more complicated in structure. The develop-
ment of this shell, by increasing the specific gravity of the animal,
rendered the simple preoral cilia of the Trochophore insufficient for
active locomotion, and the extent of the band was increased by the
region of the body on which it occurred being as it were pulled out
laterally, the characteristic velum being thus produced. Perhaps,
too, in the presence of the shell, a reason can be found for the:
absence of metameric segmentation in the Gasteropods.—Johns
Hopkins University Circulars, Oct. 1885, p. 5.
Results of a Faunistic Excursion in the Iser-, Riesen-, and Glatzer
Gebirge. By Dr. Orro Zacwartas.
With the aid of subventions from the Berlin Academy and the
Silesian Society the author has made a second excursion in the region
of the Iser-, Riesen-, and Glatzer Gebirge, and obtained some inter-
esting results, especially in relation to the Turbellaria. He has
ascertained positively that, as indicated more than fifty years ago by
Draparnaud, Dalyell, and Duges, at certain times reproduction by
spontaneous transverse division takes place in many freshwater
Planarians. In the Iser Gebirge he has found a Polycelis cornuta,
apparently identical with that described by O. Schmidt (Zeitschr.
wiss. Zool. x. 1860, pp. 25, 26), which propagates exclusively by
transverse division. In a brook near Hirschberg he obtained Pla-
naria tentaculata, Drap. (already observed by Dugés), which for
weeks together reproduced by simple division, or rather by ter-
minal gemmation. In this Planaria he ascertained by serial sections
that there was not the smallest trace of either male or female
sexual organs. He states, however, that during the autumn indi-
viduals occasionally appeared in which distinctly differentiated
sexual organs were recognizable.
Dr. Zacharias has also investigated the minute anatomy of the
Turbellaria, especially with respect to the exact course of the two
lateral nerves and the innervation of the pharynx. His investiga-
tions were made upon a new species described by him under the
name of Monotus relictus (Zeitschr. wiss. Zool. xli. 1885, p. 505).
In this species he succeeded in ascertaining the whole course of the
lateral nerves (from the cerebral ganglion to the posterior extremity
Miscellaneous. 523
of the body), and in obtaining sections which plainly showed the
penetration of offshoots of the lateral nerves into the pharynx. His
most important point is the demonstration of the existence in the
connective layer of the pharynx of a large annular ganglion, which
exceeds the true cerebral ganglion in size, and this explains the
extraordinary mobility and vitality of the pharynx, which almost
seems to be an independent creature.
The author further investigated the Cladocera and Copepoda of
the district, and also its Hydrachnide ; among the latter he notices
his discovery of a new species of the genus Sperchon, Kramer, and
of anew Arrenurus. He also obtained two new Rotatoria and an
undescribed Turbellarian (belonging to the genus Prorhynchus).—
Zoologischer Anzeiger, no. 206, p. 579d.
Note on the Blastodermic Vesicle of Mammats.
By Prof. A. C. Happon, M.A., M.R.TA.
The author suggests the view that in the blastodermic vesicle of
mammals at the close of segmentation the inner mass, since it gives
rise to the embryo proper, is perfectly comparable with the germinal
disk of a fowl during the later stages of segmentation, which has
sunk into the blastodermic vesicle owing to the absence of yolk.
The outer layer corresponds to those epiblast-cells which are
gradually enclosing the yolk, the so-called blastopore of Van Beneden
indicating in an exaggerated manner the distinction between the
embryonic and non-embryonic germinal layers. LEpiblast-cells
erow over this ‘‘blastopore” and form the covering cells (Decken-
zellen) ; eventually the invagination of the germinal area is recti-
fied, and there is a diploblastic ovum, the covering cells forming
the spurious third layer which misled Van Beneden. The segmen-
tation of the ovum is next discussed, and the conclusion is arrived
at that the first immigration of blastospheres into the interior of the
ovum (Van Beneden’s stage 3) indicates the gastrula stage. It
would further appear that this immigration was asymmetrical, much
as there is an asymmetrical invagination of the hypoblast in telole-
cithal ova. The extension of cells of the blastodermic vesicle over
the embryonic area is probably to be accounted for, in most cases, by
the sinking of the latter into the cavity of the former. These
*‘Deckenzellen” are really a portion of the blastodermie vesicle, that is
of the yolk-sac, and they form the first adhesion between the ovum
and the parent. This is compared with the impertect attachment
of the embryos of marsupials to the uterine wall, which is effected
solely by the yolk-sac, as has been recently demonstrated by H. F.
Osborn and by Caldwell.—Proc. Roy. Dublin Soc. u.s. iv. pp. 536—
547.
Note on Haleampa chrysanthellum, Peach.
By Prof. A. C. Happon, M.A., M.R.I.A.
In a paper read before the Royal Dublin Society on November 18,
1885, Professor A. C. Haddon withdrew the name applied by him
to a species of Halcampa from Malahide, co. Dublin (Proc. R. Dubl.
Soc. n. s. lv. p. 396, pl. xvi.). After having examined a number of
specimens it was found that this species is an extremely variable
one; ils synonyms are :—H. (Xanthiopus) vittata, Kef.; H.(X.) bi-
lateralis, Kef.; H. Kefersteint, Andr.; H. Andresii, Hadd. <A full
description and figure were given.
INDEX tro VOL. XVI.
ACANTHELLA, new species of, 364. °
Acanthellina, new species of, 365.
Acodia, characters of the new genus,
434,
Adamsia palliata, remarks on, 155.
Adela, new species of, 483.
_Agriophara, characters of the new
genus, 459,
Ameebe, observations on the, 215.
Amphiexis, on the new genus, 252.
aes on polymorphism in the
68.
Anisolepis, characters of the new
genus, 85,
Annelides, on Pelagic, from the Bay
of Algiers, 395.
Antennularia, new species of, &.
Aora typica, description of, 375.
Apobletes, new species of, 206.
Araneida, new species of, 257.
Archer, Mr., on a new Heliozoon,
142, 143.
Archerina Boltoni, observations on,
142, 148.
Aurela aurita, on the development
of, 398.
Axinella, new species of, 358,
Bat, on a long-tongued Pteropine,
from West Attica, 74.
Batrachians from Rio Grande do
Sul, 83; from the island of Nias,
388.
Beauregard, H., on the development
of Uantharis vesicatoria, 74.
Bell, Prof. F. Jeffrey, on two Lum-
brici with bifid hinder ends, 475.
Blane, Dr. H., on Ceratium hirun-
dinella, 444.
Blattariz, on Mesozoic, 61.
Bleptina, new species of, 424.
Blue-stone, application of the micro-
scope in the examination of, 145.
Books, new: — Mitchell’s Birds of
Lancashire, 65; Lydekker’s Indian
Tertiary and Post-Tertiary Ver-
tebrata, 66; lLydekker’s Laby-
rinthodont from the Bijori Group,
72; Year-Book of the Scientitic
and Learned Societies of Great
Britain and Ireland, 139; Bale’s
Catalogue of the Australian Hy-
droid Zoophytes, 227; Kirby’s
Elementary Text-Book of Ento-
mology, 230; Yarrell’s History of
British Birds, 390; Lansdells
Russian Ceutral Asia, 393; Wood’s
Our Insect Mnemies, 394; Fon-
taine’s Older Mesozoic Flora of
Virginia, 517,
Bothrodendron, on the relationship
of, to Sigillaria, Rhytidodendron,
Ulodendron, and Lepidodendron,
123, 162, 239.
Boulenger, G. A., on the gecgraphi-
cal distribution of the Lacertilia,
77; on heptiles and Batrachians
from the Proyince Kio Grande ao
Sul, 85; on recent contiibutions to
the herpetology of Australia, 336 ;
on Reptiles and Batrachians from
the island of Nias, 388; on new
species of Geckos, 473.
Boustield, EK. C., on Victorella pavida,
401.
Brisingidie, on the, from the ‘ Talis-
man’ expedition, 312,
Butler, A. G., on the genus Dorato-
pteryx, 51; on the blue-belted
species of Prothoé, 52; on Lepi-
doptera from Manipur and the
borders of Assam, 298, 334,
Calinaga, new species of, 309.
Callamesia, description of the new
genus, 545,
Callionymus lyra, on the oya of,
480.
INDEX.
Cambridge, Rev. O. P., on two new
species of Araneida, 2837.
Cantharis vesicatoria, on the deve-
lopment of, 74.
Carcinops, new species of, 211.
Carpenter, Dr. P. H., on the mor-
phology of the Echinoderms, and
especially of the Crinoids, 100.
Carter, H. J., on a variety of the
freshwater sponge Meyenia fluvia-
tilis from Florida, 179; descrip-
tions of sponges from Port Phillip
Heads, 8. Australia, 277, 347.
Casbia, new species of, 431.
Cephalopoda, new species of, col-
lected in the ‘Challenger’. expe-
dition, 181.
Cerapus, on certain processes formed.
by, on Tubularia indivisa, 484.
Ceratium hirundinella, observations
on, 444.
Chilomonas paramecium,
tions on, 260.
Chilton, C., on polymorphism in the
Amphipoda, 868.
Chlenias, new species of, 480.
Clania, new species of, 422.
Cockroaches, on Mesozoic, 54.
Ceelopleurus Maillardi, on the “ tag”
of, 88.
Colussa, new species of, 384.
Convoluta Schultzii, on the existence
of a new sense-organ in, 150.
Cooke, A., on the Testaceous Mol-
lusca from the Gulf of Suez, 32,
262.
Coremia, new species of, 433.
Cotylorhiza borbonica, on the deve-
lopment of, 598.
Crinoids, on the morphology of the,
100.
Crocodile-skull, on a, from the Ter-
tiary deposits of Kgeenburg, 236,
Cryptolaria conferta, observations
on, 3.
Decapoda, new, 181.
Delage, Y., on the existence of a
nervous system in the accelous
Planariz and of a new sense-organ
in Convoluta Schultzii, 150.
Dentalium, new species of, 274,
Dictyna, new species of, 237.
Dictyocylindrus, new species of, 353.
Diphasia pinaster, observations on, 5.
Diptychus, new species of, 419.
Discophlebia, new species of, 421,
Distichopora, new species of, 14,
observa-
525
Doratopteryx, on the genus, 51.
Duncan, Prof. P. M., on the “tag ”
of Ccelopleurus Maillardi, 88; on
the structure of the ambulacra of
some fossil Echinoidea, 280,
Ebonius, characters of the new genus,
209.
Kchidna hystrix, notes on the mar-
supial ege of, 479.
Echinoclathria, new species of, 292,
350, 355.
Hchinoderms, on the morphology of
the, 100; on the original funda-
mental numbers of, 399.
‘Echinoidea, on the structure of the
ambulacra of some fossil, 230.
Echinonema, new species of, 352.
Ectemnorhinus, new species of, 122.
Elasmonotus, new species of, 416.
Epicoma, new species, of, 383.
Etheridge, R., Jun., on Laceripora
cribrosa, 385.
Ettingshausen, Baron von, on the
fossil flora of Sagor, 312.
Kubolia, new species of, 452.
Eulecbria, new species of, 441.
Eumunida, new species of, 413.
EKunephrops, characters of the new
genus, 239.
Kupterote, new species of, 346.
peels M., on Adamsia palliata,
59.
Fissurella, new species of, 270,
Fistulipora, remarks on the genus,
with descriptions of new species,
496,
Flora, on the fossil, of Sagor, 312.
Folin, M. de, on a new state of Re-
ticularian Rhizopods, 232.
Foord, A. H.,on Laceripora cribrosa,
385 ; on the genus Fistulipora, 496,
Foraminifera of the Cambridge Green -
sand, on the, 149.
Foulke, Miss 8. G., on Chilomonas
paramecium, 260; on Trachelius
ovum, 477.
Freia ampulla, remarks on, 154.
Furtado, F.@’A., on instinct of orien-
tation in Helix aspersa, 519.
Galacantha, new species of, 418,
Galatheidea, on new species of, col-
lected in the ‘ Challenger’ expe-
dition, 407.
Galathopsis, characters of the new
subgenus, 417.
Gastrosteus spinachia, on the nest
and development of, 487.
526 INDEX.
Gecko, new species of, 473. from the Tertiary deposits of
Gelechia, new species of, 453.
Geological Society, proceedings of
the, 149, 250, 310.
Geophis, new species of, 87.
Gitte, Dr. A., on the development of
Aurelia aurita and Cotylorhiza
borbonica, 393.
Gruber’s, Dr., “‘ Contributions to the
knowledge of Amcebee,” on, 215.
Haacke, W., on the original funda-
mental numbers of Medusz and
Echinoderms, 399.
Haddon, Prof. A. C., on the blasto-
dermic vesicle of Mammals, 523;
on Halcampa chrysanthellum, 523.
Haleampa chrysanthellum, Peach,
note on, 523.
Halley, P., on the orientation of the
embryo and formation of the co-
coon in Periplaneta orientalis,
315.
Hanley, S., on Teredo utriculus and
other Ship-worms, 25.
Heliozoon, observations on a pre-
sumed new, 142.
Helix aspersa, instinct of orientation
in, 519.
Henderson, J. R., on new species of
Galatheidea collected during the
‘Challenger’ expedition, 407.
Herpetology of Australia, recent
contributions to the, 386.
Higginsia, new species of, 358.
Higginsia coralloides, on a new
variety of, 293,
Hiposcritia, new species of, 340.
Histeridze, new, 203.
Histiopsis atlantica, description of,
201.
Hololepta, new species of, 204.
Homopholis, new species of, 474.
Hoyle, W. E., on new species of
Cephalopoda collected in the
‘ Challenger’ expedition, 181.
Hulke, J. W., on the sternal appara-
tus in Iguanodon, 310.
Hydrozoa, on some deep-sea and
shallow-water, 1, 156.
Tdeea, new species of, 480.
Idolia, characters of the new genus,
214.
Iguanodon, on the sternal apparatus
in, 510.
Jones, Prof. T. R., on the Ostracoda
of the Purbeck formation, 251.
Kail, J. A., on a crocodile-skull
Eegenburg, 236.
Kidston, R., on the relationship of
the genera Ulodendron, L2pido-
dendron, Bothrodendron, Sigil-
laria, and Rhytidodendron, 125,
162, 239.
Lacaze-Duthiers, H. de, on Phoeni-
curus, 157.
Laceripora cribrosa,
3395.
Lacertilia, on the geographical dis-
tribution of the, 77.
Leidy’s, Prof., ‘ Freshwater Rhizo-
pods of North America,’ remarks
on, 317, 453.
Lendenfeld, Dr. R. v., on Australian
sponges, 20.
Lepidodendron, on the relationship
of, to Bothrodendron, Sigillaria,
Rhytidodendron, and Ulodendron,
123, 162, 239.
pee characters of genus,
174.
Lepidoptera from Manipur and the
borders of Assam, 298, 334; Aus-
tralian, 376, 421.
Leptognathus, new species of, 87.
Lewis, G.,{on new species of Histe-
rid, 203.
Lioderma, new species of, 206.
Lithilaria, characters of the new
genus, 425,
Lithozoa, observations on the genus,
30.
Lithyphantes, new species of, 237.
Loligo, new species of, 182.
Lumbrici with bifid hinder ends,
notes on, 475.
MacAndrew’s, R., list of testaceous
Mollusca from the Gulf of Suez,
32, 262,
M‘Intosh, Prof., notes from the St.
Andrews Marine Laboratory, 480.
M‘Murrich, J. P., on the existence of
a postoral band of cilia in Gastero-
pod Veligers, 520.
Madreporaria, on some Cretaceous,
all.
Mammals, on the blastodermic ve-
sicle of, 523. :
Marshall, W., on the Ccelenterate
nature of the sponges, 90.
Medusz, on the original fundamental
numbers of, 399.
Megaloglossus, characters of the new
genus, 74.
remarks on,
INDEX.
Metasepia, characters of the new
subgenus, 199.
Meyenia fluviatilis, on a variety of,
179.
Microdeuteropus maculatus, obser-
vations on, 370.
Microscopical Club of Dublin, pro-
ceedings of the, 140.
Mobius, Prof. K., on the nest of the
fifteen-spined stickleback, 153; on
Freia ampulla, 154.
Mollusca, testaceous, on the, from
the Gulf of Suez, 32, 262.
Moore, F., on a new species of Ze-
tides, 120.
Mosoda, new species of, 381.
Munida, new species of, 408.
Munidopsis, new species of, 414.
Murray, J. A., on a new frog from
Sind, 120.
Neorthroblattina, characters of the
new genus, 58.
Nicholson, Dr. H. A., on the genus
Fistulipora, 496.
Odontopera, new species of, 428,
Onthophilus, new species of, 213.
Ostracoda of the Purbeck formation,
on the, 231.
Ova-like structures, remarks on, pro-
cured off the Forth, 485,
Owen, Sir R., on the marsupial egg
of Echidna hystrix, 479.
Pachycreerus, new species of, 208.
Pagenstecher, Dr. H. A., on a long-
tongued Pteropine Bat, 74.
Pamphila, new species of, 378.
Papilio, new species of, 343.
Periplaneta orientalis, on the orien-
tation of the embryo and forma-
tion of the cocoon in, 315,
Perrier, H., on the Brisingide of the
‘Talisman’ expedition, 312.
Phakellia, new species of, 363.
Philenora, description of the new
genus, 382.
Philobota, new species of, 443.
Pheenicurus, observations on, 157.
Phyllomedusa, new species of, 88.
Planariz, on the existence of a ner-
vous system in the accelous,
150.
Platysoma, new species of, 207.
Plumohalichondria, new species of,
355, 367.
Plumularia, new species of, 6,
Polyzoa of the Cambridge Green-
sand, on the, 149.
527
Porpoise, notes on a female, and its
milk, 485.
Prince, E. EK., on the nest and deve-
lopment of Gastrosteus spinachia,
487,
Promachoteuthis megaptera, cha-
racters of, 182.
Prothoé, on the blue-belted species
of, 02.
Prothoé regalis, description of, 306.
Pterinoblattina, characters of the
new genus, 55.
Pterothysanus, new species of, 346.
Ptychogaster, new species of, 418.
Purdie, Prof., on the composition of
the milk of the porpoise, 486.
Quelch, J. J., on some deep-sea and
shallow-water Hydrozoa, 1, 156.
Ramsay, E. P., on the marsupial
egg of Echidna hystrix, 479.
Rana, new species of, 120.
Reptiles from Rio Grande do Sul, on
the, 85, 294; from the island of
Nias, 388.
Rhaphidonema, characters of the
order, 279.
Rhizopods, on a new state of Reti-
cularian, 232; freshwater, from
North America, on the, 317, 453.
Rhotropus, new species of, 475.
Rhytidodendron, on the relationship
of, to Ulodendron, Lepidodendron,
Bothrodendron, and _ Sigillaria,
123, 162, 239.
Rosenstock, R., on Australian Lepi-
doptera, 376, 421.
Scoparia, new species of, 427.
Scudder, S. H., on Mesozoic cock-
roaches, 54.
Scutinoblattina, characters of the
new genus, 60.
Sepia, new species of, 188.
Ship-worms, on, 25.
Sigillaria, on the relationship of, to
Rhytidodendron, Ulodendron, Le-
pidodendron, and Bothrodendron,
123, 162, 239,
Smith, 8. I, on a new crustacean,
233.
Sollas, Dr., on the classification of
the sponges, 395.
Sorocostia, characters of the new
genus, 435.
Spinachia vulgaris, on the nest of,
Sponge, freshwater, on a yariety of a,
179.
528
Sponges, on the Ceelenterate nature
of the, 90; notes on Australian,
20, 277, 347; on the classification
of the, 395.
Staurocephalus, new species of, 482.
Streptocaulus pulcherrimus, obser-
vations on, 11.
Telesto, new species of, 379,
Teredo utriculus, observations on, 25.
Terias, new species of, 338.
Testudo, new species of, 314.
Textiliforma foliata, description of,
288.
Tinea, new species of, 437.
Tomes, R. F., on some Cretaceous
Madreporaria, 311.
Tortoise, on a new species of land-,
314,
Toula, F., on a crocodile-skull from
the Tertiary deposits of Eggen-
burg, 236.
Trachelius ovum, observations on,
477.
Triballus, new species of, 212.
Truncatella, on the organization of,
396.
Turbellaria, on the anatomy of the,
522.
Ulodendron, on the relationship of,
to Lepidodendron, Bothrodendron,
Sigillaria, and Rhytidodendron,
123, 162, 239.
INDEX.
Vaillant, L., on a new species of land-
tortoise, 314.
Vayssiére, A., on the organization of
Truncatella, 396.
Veligers, on the existence of a post-
oral band of cilia in Gasteropod,
520.
Mico pavida, observations on,
401.
Viguier, C., on the pelagic Anne-
lides from the Bay of Algiers,
395.
Vine, G. R., on the Polyzoa and
Foraminifera of the Cambridge
Greensand, 149.
Wallich. Dr., notes on Dr. Gruber’s
“Contributions to the Knowledge
of the Amcebee,” 215; on Prof.
Leidy’s ‘ Freshwater Rhizopods of
North America’ and classification
of the Rhizopods in general, 317,
453.
Waterhouse, C. O., on two new Cur-
culionide, 121.
Wilsonella, new species of, 366.
Zacharias, Dr. O., on the fauna of the
Iser-, Riesen-, and Glatzer-Gebirge,
522.
Zetides, new species of, 120.
Zygophylax, characters of the new
genus, 4
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CONTENTS OF NUMBER 96. —Fi pe Series.
Page
XXXVIII. The Victorella pavida of Saville Kent. ‘By E. C.
Bousrimip, L.R.C.P. Lond. (Plate XII. figs. 1-3.)..2.....5.... SOa0E
XXXIX. Diagnoses of the new Species of Galatheidea collected.
during the ‘ Challenger ’ Expedition. By J. R. Hznperson, M.B.,
PUG oo 407
XL. Notes on Australian Lepidoptera, with Descriptions of new
Species. By Rupotpn Rosmnsrocn, B.A. ..........0....50.54-- 421
XLI. Note on Ceratiwm hirundinella (O. F. Miller), its Variability
and Mode of Reproduction. By Dr. Hen Buane. (Plate XII.
FPG ARO ea CCV ite on eee We
XLII. Critical Observations on Prof. Leidy’s ‘* Freshwater Rhizo-
pods of North America,” and Classification of the Bhiopes in. a4
general. By Surgeon-Major Watch, M.D. ................-. 453
XLII. Descriptions of three new Species of Geckos. By G. A.
WOUEENGER (06 G10 e veel sab ns he's si ce cies 8 oe ee ae 47I3
XLIV. Notice of two Zwmbrict with bifid Hinder Ends. By Prof.
Mi duwmper bern, MAL o.oo eb Go) rr 475
XLY. Trachelius ovum. By Sara GwenpoLen FoutKe
XLVI. Description of the Marsupial Egg of Echidna hystrix. By
Bowarp, 2: Ramsay, Hsq., FLIS.. C.MAZSie. vee ee ee 479
XLVI. Notes from the St. Andrews Marine Laboratory (under
the Fishery Board for Scotland). By Prof. M‘Inrosn, M.D., LL.D.,
Fik.S.; &e-—— No: Ll. “(Plate XU) jo eee 480
XLVIII. On the Nest and Development of Gastrosteus spinachia at
the St. Andrews Marine Laboratory. By Epwarp EK. Prince. .
(Plate iV) oo. oe a 0 ae OR se er
XLIX. On the Genus Fistulipora, M‘Coy, with Descriptions of
several Species. By H. Atreynz Nicnorson, M.D., D.Se., Regius
Professor of Natural History in the University of Aberdeen, and
Arrnur H. Foorp, F.G.8., late of the Geological Survey of Canada.
(Plates Vix V IIT). oe epee waco eso een 496
' BIBLIOGRAPHICAL NOTICE.
Contributions to the Knowledge of the Older Mesozoic. Flora of Vir-
ginia. By Wiitram Morris Fonrainz. Monographs of the
United States Geological Survey. Vol. VI... 233 2 acewan a eee 517
MISCELLANEOUS.
Instinct of Orientation in Helix aspersa. By F. p’A, Furtapo .... 519
On the Existence of a Postoral Band of Cilia in Gasteropod Veligers.
By JbcAvwarr M‘MuRRICH. 0.40%. 23 ee 520
* Results of a Faunistic Excursion in the Iser-, Riesen-, and Glatzer
Gebirge:, “By Dr. Orro Zacwapras 5.0057. ee eee 522
Note on the Blastodermic Vesicle of Mammals. By Prof. A. C.
mon, MieAS, MOR AC sa Oe ie al ak Oe 523
Note on Hetiaipa chrysanthellum, Peach. By Prof. A. C. Hannon,
IVA OM EA Sa ik ee dice es Ule s 2e Mel 6 eee ab.
OSes Holes MOOR herald fess one. Shawn ere she age 8 a ee 524
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