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Volume 116, Number 4

December 31, 2002

ISSN 0028-1344

CONTENTS

Diego G. Zelaya The identity of Waldo parasiticus (Dall, 1876) and

Cristian Ituarte description of Waldo trapezialis new species (Bivalvia:

G@alleoimatoxcleas ee wee cee ea ete te ede Rr ee li area 109

G. Thomas Watters The status and identity of Papyridea soleniformis

(Bimgorere, ITS) Usivelhies CawcliiGee) . 22.2 ccc5.2ctcececcascosocoasoe 118

Richard E. Petit A new Trigonostoma (Neogastropoda: Cancellariidae) from

M. G. Harasewych Mo Zam lot fe ata haf. MORES ee RN eked Bea gic one te hereon at aces er 129

Richard I. Johnson Samuel Liberty Harvey Fuller (1942-2001): a biographical

Seton ame! Imig works @m immallacolloy . ooo cc cc onsso sec eseveensctecsasaes 132

sl ee OES €9 [SF

SO Fi ft

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THE NAUTILUS 116(4):109-117, 2002

Page 109

The identity of Waldo parasiticus (Dall, 1876) and description

of Waldo trapezialis new species (Bivalvia: Galleomatoidea)

Diego G. Zelaya

Cristian Ituarte

Division of Invertebrate Zoology

Museo de La Plata

1900 La Plata, Buenos Aires

ARGENTINA

[email protected]

ABSTRACT

The epibiontic bivalve Waldo parasiticus (Dall, 1876), origi-

nally described as a leptonid species, is redescribed and figured

on the basis of shell morphology, soft-part anatomy and repro-

duction. The complete synonymy of W. parasiticus is given,

and a lectotype is designated and figured. Waldo trapezialis

new species from South Georgia Islands is described and il-

lustrated. The genus Waldo Nicol, 1966 is recognized as valid

and redescribed.

Additional key words: Antarctica, bivalves, Lepton parasiticum.

INTRODUCTION

Lepton parasiticum Dall, 1876, was described based

upon specimens living as “commensals” on irregular

echinoids collected at the Kerguelen Islands. Dall’s

(1876) original description was adequate, but without il-

lustration. Soot-Ryen (1959) reported and figured Lep-

ton cf. parasiticum from southern Chile, and Arnaud

(1964) reported L. parasiticum from Adelia Land, Ant-

arctica, and the Kerguelen Islands. Moreover, four spe-

cies with similar shell features and habitat were de-

scribed from Antarctic and Subantarctic waters: Lepton

costulatum Martens, 1885, Scioberetia australis Bernard,

1895, Solecardia antarctica Hedley, 1911, and Monta-

cuta christenseni Grieg, 1929. Their descriptions were

based mainly on shell characters, and most of them were

imprecise. With the sole exception of S. antarctica re-

ported by Miihllenhard-Siegel (1989) and Linse (1997),

none of them have been found again after their original

description. At present, as previously noted by Dell

(1990), “the relationship of Lepton [= Waldo] parasiti-

cum with similar species living in association with echi-

noderms remains uncertain”.

Waldo parasiticus has been listed under different neo-

leptonid genera: Lepton, Notolepton, Neolepton, and

Neodawisia (Dall, 1876; Arnaud, 1964; Osorio and Ba-

hamonde, 1970 and F. R. Bernard, 1983, respectively).

By studying the types of Lepton parasiticum, Nicol

(1966) found differences in shell sculpture and hinge

characters sufficient to propose Waldo, as a new genus

of Neoleptonidae. In a systematic revision of the Neo

leptonidae, Salas and Gofas (1998) excluded Lepton par-

asiticum from that family, suggesting that this species

most likely belongs to the Montacutidae or Galeomma-

tidae.

In the present paper, the placement of “Lepton” par-

asiticum Dall in the genus Waldo is confirmed, and new

data on anatomy, shell characters, reproductive biology,

and host specificity are given. In addition, Waldo tra-

pezialis new species is described.

MATERIALS AND METHODS

The specimens used in this study were collected by the

R/V Epuarpo L. HotmBerc during the 1995 cruise to

South Georgia Islands (Figure 1) and the R/V Po.Lar-

STERN during the 2002 Latin American POLARSTERN

Study (LAMPOS). Specimens were studied and figured

using scanning electron microscopy (SEM); shell mea-

surements were recorded using a stereoscopic micro-

scope equipped with micrometer eyepiece (for all cal-

culations mean and standard deviations are given). Sev-

eral alcohol-preserved specimens of Waldo parasiticus

new species were processed for histology by decalcifi-

cation in a Raillet-Henry’s solution, followed by dehy-

dration, embedding in Paraplast®, sectioning (7 wm

thickness) and staining with hematoxylin-eosin (Gabe,

1968).

Additional specimens from the National Museum of

Natural History, Washington (USNM), and others ob-

tained from dried samples of echinoids housed at the

collection of Invertebrates, Museo Argentino de Cien-

cias Naturales “Bernardino Rivadavia” (MACN) were

studied. Type specimens of Lepton parasiticum

(USNM), and Montacuta christenseni from Bergen Mu-

seum, Norway (BM), were studied. The type material of

Scioberetia australis (consisting of fragments of one

shell, two 1 mm-long juveniles and a series of histolog-

Page 110

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Figure 1. Location map. ®): localities for Waldo parasiticus

(this work); @: other known records for W. parasiticus; : lo-

calities for Waldo trapezialis new species.

ical sections) from the Muséum National d’Histoire Na-

turelle, Paris (MNHN) were also used for comparative

purposes.

SYSTEMATICS

Genus Waldo Nicol, 1966

Description: Shell small (up to 4.1 mm), extremely

fragile, elongate-oval or subquadrangular, equiv alve,

gapping at anterior, posterior and ventral margins. Shell

surface smooth or with radial ribs. Hinge edentulous in

adults; ligament internal, strong, and tenn periostra-

cal ligament present. Mantle border expanded beyond

the shell margin, bearing a variable number of stout ten-

tacles. Free edges of mantle border expanding anteriorly

in a temporary inhalant structure; only exhalant siphon,

present. Only one demibranch, the inner, present. Foot

cylindrical, with a well-marked heel and strong byssal

gland. Epibionts on irregular echinoids.

THE NAUTILUS, Vol. 116, No. 4

Waldo parasiticus (Dall, 1876)

(Figures 2-22)

Lepton parasiticum Dall, 1876: 45-46.

Lepton costulatum Martens, 1885: 94;

1886: 115 (South Georgia Islands).

?Solecardia antarctica Hedley 1911: 4, pl. 1, fig.5; Miihlen-

hard-Siegel, 1989: 164, pl. 3, fig. 28, pl. 7, fig. 28: Linse,

1997: 55, pl 2, figs.1-3 (Cape Royds).

Montacuta Wirironenn Grieg, 1929: 14 (Admiralty Bay, South

Shetland Islands).

Lepton cf. parasiticum.—Soot-Ryen, 1959: 49, pl.

Notolepton parasiticum.—Amaud, 1964: 55—60.

Neolepton parasiticum.—Osorio and Bahamonde, 1970: 221

Neodavisia parasiticum.—Bernard, 1983: 33; Ramirez-Béhme,

1993: 136

Waldo parasiticus.—Nicol, 1966: 59-61, pl. 8, fig. 5 and pl. 9,

figs. 5-7.

Martens and Pfeffer,

ey ince, MS),

Description: Shell small (maximum shell length 4.1

mm), moderately inflated (mean shell width/shell

height ratio 0.6 + 0.06, n = 11). Shell extremely thin,

cin, translucent, shiny. Shell outline ovate, elongate

(shell height/shell length ratio: 0.69 + 0.04, n = 1D),

slightly inequilateral, beaks subcentral, not prominent

(Figures 2-4). Anterior end rounded and slightly pro-

jecting, posterior end truncate (less markedly in juve-

niles), slightly oblique (Figures 4, 5). Dorsal margin

straight or slightly and evenly arcuate, posterior margin

straight, ventral margin slightly and evenly curved,

crenulate. Valves gaping ventrally and at anterior and

posterior ends (Figures 8-10). Nepionic shell (approx-

imately 470 jm length), inflated, forming a rounded

cup (Figure 11), clearly demarcated by a commarginal

rim (Figure 12). Shell surface sculptured with 30-35

relativ ely well-marked radial ribs and irregular com-

marginal ribs, both fading towards the beaks. Radial

ribs often very evident in small-sized specimens, tend-

ing to fade in adults. Hinge edentulous in adults. Lig-

ament internal, strong; Bernal periostracal ligament

present (Figures 13-16).

D-shaped larvae with two well-developed lamellar lat-

eral teeth in the right valve, the anterior long and slen-

Figures 2-3. Waldo parasiticus. Lectotype,

USNM 11907.

3. Posterolateral view showing the exhalant

Right lateral view.

siphon and the unpaired tentacle above the siphon. f: foot; s: siphon; t: tentacle. Scale bars = 1 mm.

D. G. Zelaya and C. Ituarte, 2002

Page 111

Figures 4-12. Waldo parasiticus from South Georgia Islands, MLP 6505. 4. Outer view of an adult specimen. 5. Outer view of

a juvenile. 6. Lateral view of a living specimen showing the anterior extention of the mantle border. 7. Ventral view of a specimen

showing the anterior mantle projections and paired tentacles along the ventral mantle border. 8. Anterior shell gap. 9. Ventral shell

gap. 10. Posterior shell gap. 11. Detail of the nepionic shell. 12. Detail of the zone between nepionic shell and dissoconch. Scale

bars: Figures 4-10 = 1 mm; Figures 11-12 = 100 pm.

Page 112

THE NAUTILUS, Vol. 116, No. 4

Figures 13-19.

Waldo parasiticus. 13-15. Isla de Los Estados, MACN 22219; 16-19. South Georgia Islands, MLP 6505. 13.

Inner view of a left valve. 14, 15. Details of the hinge. 16. Inner view showing the internal ligament. 17. Inner view of the right

valve of a larva removed from adult. 18. Right valve of a larva, detail of the hinge. 19. Left valve of a larva, detail of the hinge. L:

internal ligament. Scale bars: Figure 13 =

der, the posterior shorter and stronger; in the left valve

two slightly marked fossettes to receive right laterals.

Larval ligament internal, strong, short, somewhat trian-

gular (Figures 17-19).

Anatomy: Mantle margins free for about the % of its

length, fused at posterior end forming a relatively short

pre siphon: ul suture. Only the exhalant aperture, extend-

ed in a short siphon, present (Figure 3). Mantle border

extending beyond shell margin, covering the surface of

the valves. The free edges of the Tent extend anteri-

orly and upwards forming a partly closed channel serving

as a temporary inhalant “siphon” (Figures 6, 7). Ventral

1 mm; Figures 14-15, 17-19 = 100 wm; Figure 16 = 500 pm.

mantle border with long and stout cylindrical tentacles:

1 unpaired tentacle (just over the exhalant siphon) and

7 paired tentacles, alternate or opposite (5 pairs at sides

of the pedal aperture, 1 at the point of mantle border

fusion, and 1 posterior to the mantle border fusion, on

the presiphonal suture) (Figures 3, 7). Only one, the

inner, demibranch present, ascending lamella shorter

than the descending one, with few interlamellar junc-

tions; the suprabranchial space serves as brood space

(Figures 20-22). Foot cylindrical (short when retracted)

with a blunt heel and well-marked byssal groove running

along the ventral foot surface. A strong byssal gland lo-

D. G. Zelaya and C. Ituarte, 2002

Page 113

Figures 20-22. Histology of Waldo parasiticus (South Georgia Islands, MLP 6505). 20. Transverse section at the posterior end

of the visceral mass. 21. Transverse section at the anterior half of the visceral mass. 22. Detail of the free mantle border. al:

ascending lamella of inner demibranch; bs: brooding space; dl: descending lamella of inner demibranch; id: inner demibranch; m:

mantle; mf: expanded mantle fold; p: periostracum; po: pedal opening r: rectum; t: tentacle. Scale bars: 200 wm.

cated at the base of the heel secreting a byssus of 3 to

5 filaments.

Type Locality: Kerguelen Islands.

Material Examined: Lectotype (here designated)

(Figures 2, 3) and numerous paralectotypes (>50 se-

verely damaged specimens and loose valves) of Lepton

parasiticum (USNM 11907); syntypes of Montacuta

christenseni (BM 35268 and 35270) (mostly decalcified);

numerous specimens from Deception Island, Bransfield

Strait, South Shetland Islands (USNM 613095), and

54°18’ S, 35° 30’ W, South Georgia Islands, 94 m, 8 April

1996 (MLP 6505, MACN 35017); 2 specimens, South

Georgia Islands (MACN 18715); several loose valves,

Isla de los Estados (MACN 22219); 10 specimens,

54°27' S, 35°41’ W, South Georgia Islands, 249-256 m,

12 April 2002 (MLP 6729): 4 specimens, 60°59’ S, 43°

27' W, South Orlmeys Islands, 399-402 m, 22 April 2002

(MLP 6731) (Figure 1).

Other Published Records: Southern Chile: 41°58’ S,

73°18’ W, Golfo de Ancud (200 m); 41°43’18" S,

72°38'15" W, Estero Reloncavi (470 m); 41°38'34” S,

72°22'45" W, Estero Reloncavi (50 m) (Soot-Ryen,

1959); Antarctica: Adelia Land (Amaud, 1964) (Figure

ih),

Distribution: Antarctic and Subantarctic waters, 50—

470 m.

Remarks: Diagnostic characters of Waldo parasiticus

are: the extremely thin shell, gaping ventrally and at an-

terior and posterior ends, beaks with a well-marked ne-

pionic shell, adult hinge edentulous with internal liga-

ment, shell surface sculptured with radial ribs and com-

marginal ribs, and expanded mantle border covering the

outer shell surface bearing long and stout tentacles.

The syntypes of Montacuta christenseni (despite being

strongly decalcified) were found to be identical in shell

morphology and soft part anatomy to Waldo parasiticus.

Smaller syntypes differed slightly in having strongly

marked radial ribs.

The original description of Lepton costulatum Mar-

tens, 1885, and its redescription by Martens and Pfeffer

(1886) are rather poor and lack illustrations. Despite

this, they are informative enough to indicate that L. cos-

tulatum is conspecific with W. parasiticus. Unfortunate-

ly, the types of L. costulatum, originally housed at Mu-

seum fiir Naturkunde, Berlin (ZMB 37468), seem to be

lost (M. Glaubrecht, in litt., June 2001).

Solecardia antarctica Hedley, 1911, a species reported

from the Antarctic Region, is also similar to W. parasi-

ticus and, based on the information given by the original

description and figure, they seems to be conspecific, as

previously suggested by Arnaud (1964).

Lepton costulatum and Montacuta christenseni were

previously proposed as synonyms of Lepton parasiticum

by Soot-Ryen (1959).

Biological observations: Waldo parasiticus is a di-

oecious species. Females produce large, non-plankto-

trophic yolky eggs, which are incubated in the space lim-

ited by the descending lamella of the inner demibranch

and the visceral mass. Larvae, occurring free in the vol-

ume of the brooding space, were found in April and

November in specimens larger than 1.5 mm. A maxi-

mum number of 157 D-shaped larvae (0.45/0.5 mm

length X 0.4/0.5 mm width), all in the same develop-

mental stage, were found in a maternal individual of 2.7

mm long. Waldo parasiticus lives as an epibiont, secured

by the byssus to the spines in the ambulacral areas of

numerous irregular Antarctic and circumantarctic Schi-

zasteridae echinoids (Table 1). The epibiotic behavior in

association with large invertebrates (referred to as sym-

biosis, commensalism or parasitism by different authors)

is characteristic of many Galeommatoidea. While the

Page 114

THE NAUTILUS, Vol. 116, No. 4

Figures 23-28.

Waldo trapezialis new species. 23. Holotype (MLP 6728-1), left lateral view. 24-28. Paratypes (MLP 6728-2).

24. Detail of the nepionic shell. 25. Ventral view of a left valve showing ve sntral gap. 26. Posterior view. 27. Anterior end showing

a portion of the mantle fold (much retracted) covering the shell. 28. Detail of the hinge showing the internal ligament. L: internal

ligament. Scale bars: Figures 23, 25, 26 = 1 mm; Figures 24, 28 = 100 pm; Figure 27 = 500 pm.

vast majority of galeommatids have been reported to live

on crustaceans, members of the Montacutidae were

mainly fejoomnted! associated with irregular echinoids

(Coan et al., 2000: Mikkelsen and Bieler, 1992: Ponder,

1968; Deroux, 1961; Popham, 1940).

Species erroneously identified as Waldo parasiti-

cus: Mortensen (1943) reported specimens of “white

mussels” attached to spines of the echinoid Sterechinus

diadema from Kerguelen Islands; these specimens were

later reported by Ammen (1964) as Notolepton parasi-

ticum. However, Mortensen’s (1943) figures suggest that

the specimens likely belong to Lissarca notorcadensis

Melville and Standen, 1907.

Powell (1957) erroneously reported specimens of a true

Neoleptonidae as Notolepton parasiticum (Dall). Speci-

D. G. Zelaya and C. Ituarte, 2002

Table 1. Echinoid species reported as hosts for Waldo parasiticus.

Species (original designations) Host

Lepton parasiticum

Lepton costulatum

Tripylus sp.

spatangoid echinoids

Lepton sp. Abatus cavernosus

Abatus agassizti

Lepton parasiticum Abatus cordatus

Montacuta christenseni Abatus cavernosus

Lepton cf. parasiticum

Notolepton parasiticum

Waldo parasiticus

Triphylaster philippii

Abatus bidens

Abatus agassizii

Source

Dall, 1876

Martens, 1885; Martens and

Pfeffer, 1886

Mortensen, 1910;

Mortensen, 1936

Thiele, 1912

Grieg, 1929

Mortensen, 1936

Soot-Ryen, 1959

Arnaud, 1964

present work

Page 115

Waldo parasiticus

mens reported and figured by Dell (1964) as Neolepton

parasiticum (Dall) also correspond to a neoleptonid.

Waldo trapezialis new species

(Figures 23-28)

Description: Shell small (maximum shell length 2.9

mm), trapezoidal, somewhat inflated (shell width/shell

height ratio: 0.73 + 0.12, n = 7), relatively high (shell

height/shell length ratio: 0.74 + 0.03, n = 7); gapping

widely at ventral margin and only slightly at anterior end

(Figures 25, 27). Shell extremely thin, white, shiny. Shell

inequilateral, slightly inequivalve (Figure 26). Beaks sub-

central, slightly displaced forward (located at around

45% of shell length), not prominent (Figure 23). Ne-

pionic shell (approximately 590 jzm length) well-marked,

inflated, forming a cup (Figure 24). Anterior end low,

widely rounded, posterior end high, evenly arcuate. Dor-

sal margin markedly sloping forward, wide and evenly

arcuate, ventral margin long, straight and smooth. Shell

surface smooth. Hinge dental ones in adults. Internal lig-

ament, strong, saddle-shaped (Figure 28), external per-

iostracal ligament present.

Anatomy: Mantle margins free at about the 3/4 of its

length, with large pedal aperture; posterior end of the

mantle forming an exhalant aperture extended in a short

siphon. Mantle border extended beyond the shell mar-

gin, covering at least partially the shell surface. At the

anterior end, the free edges of the mantle extend to

form a temporary inhalant structure, a partly closed

channel directed upwards. Along the ventral border of

the mantle 5 pairs of opposite long and stout cylindrical

tentacles, present: 3 at sides of the pedal aperture, 1 at

the point of mantle fusion, and 1 posterior to the fusion,

on the presiphonal suture. Only one, the inner, demi-

branch present. Foot cylindrical with a blunt heel and

well-marked bysal groove running along its ventral sur-

face. A strong byssus gland located at the base of the

foot heel secretes a multifilamentous byssus; each one

of the byssus filaments provides anchorage to one spine

of the host, an irregular echinoid.

Triphylus excavatus

present work

Type locality: 54°18’ S, 35°30’ W, South Georgia Is-

lands, 94 m (Figure 1).

Type material: Holotype (MLP 6725-1) (2.45 x 1.9

mm), 3 paratypes (MACN 35016) (2.9 X 2.0 mm, 1.7

xX 1.35 mm and 1.6 X 1.25 mm) and 2 paratypes (MLP

6728-2) (2.45 X 1.8 mm and 2.9 x 2.2 mm) all from

type locality, 8 April 1996; 1 paratype, 54°27’ S, 35°41’

W, South Georgia Islands, 249-256 m, 12 April 2002

(2.55 X 1.8 mm) (MLP 6730).

Distribution: South Georgia Islands.

Etymology: The name refers to the trapezoidal shell

outline.

Remarks: Waldo trapezialis new species can be easily

identified by its trapezoidal shell shape, smooth shell

surface, and shell border not crenulated. W. t) “apexialis

differs from W. parasiticus in having a more inflated,

slightly inequiv alve shell, with a long smooth and straight

ventral mar gin, high broadly arcuate posterior end, and

surface without Pail sculpture or commarginal ribs.

The nepionic shell is larger in W. trapezialis. W. trape-

zialis also differs from W. parasiticus in lacking the un-

paired tentacle above the exhalant siphon.

The specimens of Waldo trapezialis new species stud-

ied were collected attached to loose spines of an irreg-

ular echinoid. We do not have at this point further de-

tails on the identification of the host species.

THE SYSTEMATIC POSITION OF WALDO

The genus Waldo was proposed by Nicol (1966) to in-

clude Lepton parasiticum Dall, and was tentatively as-

signed to the family Neoleptonidae. The presence of

only one pair of demibranchs clearly exclude Waldo

from the Neoleptonidae. Salas and Gofas (1998), in a

revision of the genus Neolepton, suggested that Waldo

parasiticus most likely belongs to the Montacutidae or

Galeommatidae. However, the lack of hinge teeth in the

adults, the presence of stout tentacles as mantle projec-

tions, and the dioecious condition are characters not pre-

viously reported for members of the Montacutidae. At

Page 116

present there is not agreement on the suprageneric clas-

sification of the Galeommatoidea. Vokes (1980) recog-

nized five families of Galeommatoidea: Kellidae, Erycin-

idae, Leptonidae, Montacutidae and Galeommatidae,

while Coan et al. (2000), recognized only two galeom-

matoid families: Lasaeidae (which includes Montacuti-

dae) and Galeommatidae. Due to this and to the lack of

a clear definition of families, a decision about the supra-

generic placement of Waldo is postponed.

Waldo parasiticus resembles Scioberetia australis F.

Bernard, 1895, a species obtained from the ambulacral

areas of the echinoid Tripylus excavatus from Cape

Horn (southern South America). The species was never

recorded again after its original description; however,

Bernard's (1895a) record was subsequently repeated by

Thiele (1912), Arnaud (1964), Osorio and Bahamonde

(1970), F. R. Bernard (1983), and B6hme (1993). Ac-

cording to the generic diagnosis of the genus Scioberetia

given by Thiele (1934), Waldo would be its synonym.

However, from Bernard’s (1895a) original description

and from the study of the type material of S. australis

(MNHN), it is clear that this genus differs from Waldo

by the presence of a well-developed taxodont-like larval

hinge teeth (Bernard, 1895a), the lack of byssus gland

anal by the absence of tentacles on the mantle border.

The probable hermaphroditic condition discussed by

Bernard (1895a—c) would be an additional differential

character. In our opinion, both Scioberetia and Waldo

should be considered as valid genera.

ACKNOWLEDGMENTS

The authors wish to thank D. Nahabedian for providing

the specimens collected by the R/V Epuarpo L. HoLm-

BERG. We are grateful also to M. G. Harasewych and T.

Nickens (National Museum of Natural History, Wash-

ington, DC, USA), V. Héros and P. Bouchet (Muséum

National d'Histoire Naturelle, Paris, France), and J. A.

Kongsrud (University of Bergen, Museum of Zoology,

Bergen, Norway) who kindly facilitated the study of type

specimens. M. Glaubrecht (Museum fiir Naturkunde,

Berlin, Germany) kindly commented on the types of

Lepton costulatum, and A. Tablado allowed access to the

MACN collections. Michael Schrédl provided photo-

graphs of living specimens taken aboard the R/V PoLar-

STERN, and Rafael Urréjola (from the MLP Scanning

Electron Microscopy unit) for his technical assistance

and fine work with SEM photography; their help is al-

sogreatly apreciated. The authors are members of the

National Research Council for Science and Technology

(CONICET), Argentina. This work was partially sup-

ported by a gr ant from Fundacién Antorchas to D. Z.

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THE NAUTILUS 116(4):118-128, 2002

Page 118

The status and identity of Papyridea soleniformis

(Bruguiére, 1789) (Bivalvia: Cardiidae)

G. Thomas Watters

Department of Evolution, Ecology,

and Organismal Biology

Museum of Biological Diversity

Ohio State Univer sity

1315 Kinnear Road

Columbus, OH 43212 USA

ABSTRACT

The name Papyridea soleniformis (Bruguiére, 1789), as used

by most authors, embraces two taxa of marine cardiids found

in the tropical Atlantic Ocean. Papyridea lata (Born, 1778) oc-

curs in the western Atlantic Ocean, Caribbean Sea, and Gulf

of Mexico. Born’s specimen in the Zoologisches Museum, Vi-

enna, labeled as variety “roseo-maculata” (891a), is here des-

ignated as the lectotype. Papyridea soleniformis (Bruguiére,

1789) is sympatric with P. lata, but also occurs in the eastern

Atlantic Ocean. Chemnitz, 1782, Conchylien Cabinet, page 65,

plate 6, figures 49 and 50 are designated as the lectotype il-

lustrations. Cardiuwm (Papyridea) spinosum var. turtoni Dall,

1900 is a junior synonym of P. soleniformis.

Additional key words: Cardioidea, type specimen, Atlantic

Ocean.

INTRODUCTION

The marine cardiid known as Papyridea soleniformis

(Bruguiere, 1789) is considered a fairly common, wide-

spread species in the western Atlantic Ocean, Caribbean

Sea, and portions of the eastern Atlantic Ocean. Addi-

tional study has revealed the presence of two taxa cur-

rently grouped under that name: Papyridea soleniformis

(Bruguiére, 1789) and Papyridea lata (Born, 1778). The

source of the taxonomic confusion concerning these spe-

cies may be traced to Linnaeus (1758). He described

Solen bullatus from an unknown locale with reference

to Rumphius’s plate 44, fig. N (Figure 1). However, Lin-

neaus’s brief description of Solen olllatens does not apply

to this illustration. (I have cited Rumphius (1705) for

this figure, but as Dodge (1952) pointed out, we cannot

be sure which edition, or even which of Rumphius’s two

works, Amboinische Rariteitkamer or Thesaurus imagin-

um piscium Testaceorum, was involved. Regardless, the

plates of the two works are identical.) The species de-

picted in Rumphius’s fig. N also does not conform to

Linnaeus’s concept of Solen as evidenced by the other

species originally included by him in that genus. Smith

(1945) identified the figure with a Pacific species of Ful-

via. But the color plate in Rumphius is of an all-white

shell, which would be rare for a Fulvia. Furthermore,

Rumphius used the vernacular name Doublet or Dub-

beld for other cardiids and the name Ark for arcids.

Rumphius called the species later named by Linnaeus

as the Bastaard Ark. Based on this evidence, Rumphius’s

species undoubtedly is an arcid. Schumacher (1817) be-

lieved Linnaeus’s species was misplaced in Solen and

suggested Coeur (a cardiid). Hanley (1855) agreed but

suggested that the description applied to a Fulvia and

the illustration to an arcid. Dodge (1952) concluded that

Linnaeus mistakenly had given Rumphius’s fig. N as rep-

resenting this species. In any event, the species cannot

be identified unambiguously from either the description

or the illustration and no type exists in the Linnean col-

lection (Dodge, 1952). The name Solen bullatus there-

fore is anomen dubium. However, many subsequent au-

thors retained bullatus for various species and ignored

Linnaeus’s incongruous description. Inasmuch as we do

not know the identity of Linnaeus’s species, no use of

the name Solen bullatus can be accepted as a correct

identification, and none of the subsequent authors may

be considered the author of that name, even if placed

in a different genus (ICZN, 1999: Art. 49). Finally, Rum-

phius’s fig. N does not resemble either of the two Pa-

pyridea species discussed here and appears to be an ar-

cid.

MATERIALS AND METHODS

Fifty-six specimens of P. soleniformis and 325 specimens

of P. lata were examined. Specimens were measured as

the greatest length parallel to the hinge axis. Institutional

acronyms are: ANSP, Academy of Natural Sciences, Phil-

adelphia, USA; GTW, collection of G. Thomas Watters,

Columbus, Ohio, USA; HGL, collection of Harry G.

Lee, Jacksonville, Florida, USA; RV, collection of Ron

Voskuil, Delft, The Netherlands; UF = Florida Museum

of Natural History, Gainesville, Florida, USA; UMMZ =

University of Michigan Museum of Zoology, Ann Arbor,

G. T. Watters, 2002 Page 119

S :

Se NLS

ae NG

Naw

Figures 1-6. 1. Rumphius, 1705, pl. 44, fig. N. Type figure of Solen bullatus Linnaeus, 1758. 2. Pectunculus tenuis pelluci-

dus... Lister, 1685, pl. 342, fig. 179. Type figure of Coeur spinosum Meuschen, 1787 = Papyridea lata (Born, 1778). 3. Blasen-

arrige Herz Knorr, 1772, pl. 7, fig. 6. Cited by Born as questionable figure of Cardiwm latum Bom, 1778. 4. Born, 1780, pl. 3,

fig. 8. Born’s refiguring of Cardium latum Born, 1778. 5. Chama H. inaequilatera, oblique striata... Gualtieri, 1742, pl. 85, fig.

H. Type figure of Coeur hiatus Meuschen, 1787 = Papyridea soleniformis (Bruguiére, 1789). 6. Solen bullatus “Linnaeus.”

Chemnitz, 1782, 65, pl. 6, figs. 49, 50. Lectotype figure of Cardium soleniforme Bruguiére, 1789, designated herein.

Michigan, USA; USNM = National Museum of Natural

History, Washington, DC, USA.

SYSTEMATICS

Superfamily Cardioidea Lamarck, 1809

Family Cardiidae Lamarck, 1809

Subfamily Trachycardiinae Stewart, 1930

Genus Papyridea Swainson, 1840

Type Species: Papyridea Soleniforme “Wood,” non

Bruguiére, 1789, by subsequent designation of Gray

(November, 1847). Swainson had included four species

under Papyridea, including Papyridea soleniforme

“Wood, 1815.” Wood's figure (pl. 56, fig. 3) is of Papyr-

idea lata (Bom, 1778). Swainson’s type species is there-

fore misidentified. But as both species are members of

Papyridea, there is no threat to the stability of this genus

name, and I have not referred the case to the Commis-

sion (ICZN, 1999: Art. 70 (b)). Herrmannsen (Septem-

ber, 1847) had earlier designated Cardium bullatum as

type of Papyridea, but as that species was not included

by Swainson in his original list, it is not eligible as the

type species.

Papyridea lata (Born, 1778)

(Figures 2, 4, 7-13)

Pectunculus tenuis pellucidus, leviter purpurascens, dense

striatus a Jamaica Lister, 1685: pl. 342, fig. 179 [pre-Lin-

nean; type figure of Coeur spinosum Meuschen, 1787, by

restriction of Clench and Smith, 1944, as first revisors].

Cardium latum Born, 1778: 37; 1780: pl. 3, fig. 9; Bruguiére,

1789: 234-235 [partim].

Coeur spinosum Meuschen, 1787: 442 [non-binomial].

Cardium soleniforme “Bruguiére”. —Wood, 1815: 233, pl. 56,

fig. 3; 1835:56, fig. 3; 1856: 5, pl. 5, fi

guiére, 1789].

Papyridea Soleniforme “Wood”.—Swainson, 1840: 374.

Cardium (Papyridea) bullatuwm (Linnaeus)—Romer, 1869: 74—

76, pl. 12, figs. 13-16.

Cardium latum “Chemnitz”.—Brauer, 1878: 127.

Cardium (Papyridea) bullatum “Chemnitz” —Kobelt, 1880:

345, pl. 101, fig. 4.

Cardium spinosum var. spinosum (Meuschen).—Dall, 1900b:

1107-1108.

Papyridea spinosum (Meuschen).—Smith, 1937: 49, pl. 17, fig.

8: McLean, 1939: 164-165, pl. 24, figs. 3, 9; Vilas and

Vilas, 1945: 38, pl. 3, fig. 15.

Papyridea hiatus (Meuschen).—Clench and Smith, 1944: 17,

pl. 4, figs. 3-5 [partim].

Papyridea hiatus (Meuschen).—McLean, 1951: 71 [partim|]

[not pl. 15, fig. 1 = Papyridea soleniformis (Bruguieére,

1789)].

Papyridea soleniformis (Bruguiére).—Keen, 1937: 14-15; Ab-

bott, 1954: 398, pl. 39n [partim]; Perry and Schwengel,

1955: 68, pl. 13, fig. 74: Warmke and Abbott, 1961: 183,

pl. 37j; Abbott, 1968: 228, fig. 7; Nordsieck, 1969: 103,

pl. 15, fig. 57.10; Stanley, 1970: 157, 158, pl. 20, figs. 1-

6; Porter and Tyler, 1971: 16, fig. 9; Clench, 1973: 57, pl.

23, fig. 16; [partim] Abbott, 1974:484, pl. 22, fig. 5555;

Humfrey, 1975: 245, pl. 29, figs. 18, 18a.; Rios, 1975: 223,

pl. 71, fig. 1072; Keen, 1980: pl. 5, fig. 7 [partim]; Vokes

and Vokes, 1983: 40, 63, pl. 41, fig. 5; Rios, 1994: 263, pl.

90, fig. 1282 [all non Bruguiére, 1789].

Cardium bullatum “Chemnitz”. —Lamy, 1941: 462-463 [par-

tim].

Papyridea (Papyridea) soleniforme (Bruguiére )—Fischer-Piet-

te, 1977: 69-70 [partim].

Papyridea latum (Bom).—Voskuil and Onverwagt, 1991: 31

[partim].

Papyridea (Papyridea) lata (Born).—Kafanov, 1997: 3-4, pl. 1,

figs. 3a, b, pl. 2, figs. la-d, 2a-e, pl. 3, figs. la-c.

g. 36 [all non Bru-

Page 120 THE NAUTILUS, Vol. 116, No. 4

Figures 7-13. Papyridea lata (Born, 1778). 7. Lectotype, herein designated (Zoologisches Museum, Wien, 891a) (from original

photograph of R. Voskuil). Locality unknown. 8. Paralectotype, herein designated (Zoologisches Museum, Wien, 891a) (from

original photograph of R. Voskuil). Locality unknown. 9. 2-12 m, Cat Cay, Bimini, Bahamas (UF 176315) (47 mm). 10-

11. Beached, Sanibel Island, Florida, USA (GTW) (34 mm). 12. Salvador, Bahia State, Brasil (HGL) (36 mm). 13. Matanzas,

Cuba (GTW) (31 mm).

Figures 14-21. Papyridea soleniformis (Bruguiére, 1789). 14-15. Syntype of Cardium (Papyridea) spinosum var. turtoni Dall,

1900. [Pleistocene] of Caloosahatchee River, Florida, USA (USNM [USGS] 157547) (42 mm). 16-17. Sao Tomé (ANSP 267835)

(53 mm). 18. St. Helena (USNM 777907) (43 mm). 19. Cape Verde Islands (ANSP 309062) (45 mm). 20. Water Island, Virgin

Islands (GTW) (33 mm). 21. Off Lake Worth, Florida, USA, 60 m (UF 12117) (34 mm).

G. T. Watters, 2002

Description: Shell to 44 mm in length, thin but solid,

oval, compressed, slightly opisthogyrate, slightly inequi-

lateral, with the umbo located 37-45% length back from

the anterior margin. Posterior of umbones rounded,

lacking a ridge or angulation. Shells gaping antero-ven-

trally and postero-dorsally, forming pedal and siphonal

gapes respectively. Exterior of shell ornamented with

43-59 primary radial ribs. Ribs about as wide as inter-

rib spaces on anterior of shell, becoming wider on pos-

terior. Postero-dorsal margin dentate. Primary ribs tri-

angular in cross-section on anterior of shell, becoming

flattened on posterior of shell. Anterior-most primary

~18 ribs and posterior-most ~12 ribs ornamented with

minute concave scales. Scales cross entire rib on anterior

ribs, but are situated on a narrow medial line on the

posterior ribs. Exterior color quite variable. Background

white with large irregular patches of yellow, orange, rose,

or purple, sometimes forming irregular concentric

bands. Occasional specimens are uniformly colored with

these shades. Some specimens have one or two vague,

broad rays radiating from the umbones of the same color

as the patches. These rarely persist on the exterior on

specimens larger than 10 mm. Living and freshly dead

specimens have a thin, tan-colored periostracum around

the shell margin. Hinge occupying 1/2 of total length.

Anterior laterals larger, more blade-like than posterior

ones. Left and right laterals of equal size. Left laterals

engage dorsal to right laterals. Small, peg-like left car-

dinal tooth fits into socket in right valve. Ligament ex-

ternal, small, approximately 1/6 or less of shell length.

The arrangement of the teeth and ligament allows the

shells to rock along an antero-postero axis (Watters,

1992). Interior of shell white, with exterior colors show-

ing through. The two broad rays radiating from the

umbo are much more conspicuous and noticeably longer

on the interior than on the exterior.

Preserved examples have not been seen.

Type Material: The Born collection in the Zoolo-

gisches Museum, Wien, has two syntypes of Cardium

latum (891a), one labeled “roseo-maculata,” the other

“luteo-maculata” (Voskuil, in litt.). The first, ”roseo-ma-

culata,” corresponds best to Born’s 1780 illustration and

is here designated as the lectotype (Figure 7). The sec-

ond specimen, “luteo-maculata,” is a paralectotype (Fig-

ure 8). ICZN (1999: Art. 72.4.1) does not allow speci-

mens “expressly” excluded as distinct variants to remain

part of the type series. Strictly speaking this might ex-

clude Born’s two color variants from being primary

types. However, it is clear that Born considered all of

his specimens to belong to one or the other color variant;

the two variants therefore compose the entire type se-

ries.

Type locality: Cardiuwm latum Born, 1778: unknown.

Material examined: BERMUDA: 1.5-3.0 m, Coney

Island (GTW, HGL). TEXAS: 46 m off Freeport

(ANSP). SOUTH CAROLINA: Myrtle Beach, Orry Co.

(GTW). FLORIDA [Atlantic Ocean]: dredged 90 m

Page 121

(RV); 21 m, 121 km E of St. Augustine, St. Johns Co.

(UF); 320 m, off St. Augustine, St. Johns Co. (GTW);

23 km ENE of Mayport, Duval Co. (HGL); 27 m, 32

km E of Mayport, Duval Co. (HGL); 30-60 m, off Sing-

ers Id., Palm Beach Co. (UF); 30 m, Peanut Island, Palm

Beach Co. (UF); Palm Beach, Palm Beach Co. (UF);

Fish Haven, Lake Worth, Palm Beach Co. (UF); Lake

Worth, Palm Beach Co. (ANSP, GTW, UF): S of Lake

Worth Inlet, Palm Beach Co. (UF); 55 m, off Boynton

Inlet, Palm Beach Co. (UF); 18 m, off Briny Breezes,

Palm Beach Co. (UF); fill from 18 m, Pompano Beach,

Broward Co. (UF); Finger Channels, Dade Co. (HGL);

Bear Cut, Key Biscayne, Dade Co. (UF); Biscayne Bay,

Dade Co. (GTW); 73 m, off Miami, Dade Co. (GTW);

Little Duck Key, Monroe Co. (UF); W end Bahia Honda

Key, Monroe Co. (UMMZ); Newfound Harbor Keys,

Monroe Co. (UF); 117 m, Florida Straits, 24°23°15” N,

82°01717” W (UF). [Gulf of Mexico]: 64 m, 150° off Pen-

sacola, Escambia Co. (UF); off Destin, Okaloosa Co.

(ANSP); 26 m, Destin, Okaloosa Co. (UF); 40 m, 225°

off Panama City, Bay Co. (ANSP, UF); 8-11 km S of

Alligator Point, Franklin Co. (UF); Boca Ciega Beach,

Pinellas Co. (UF); St. Petersburg, Hillsborough Co.

(UF); Longboat Key, Sarasota Co. (UF); 13-15 m, 15-

18 km SW of Big Sarasota Pass, Sarasota Co. (UF); Ft.

Myers Beach, Lee Co. (ANSP); Captiva Island, Lee Co.

(UF); Point Ybel, Sanibel Id., Lee Co. (UF); Sanibel Id.,

Lee Co. (ANSP, GTW, UF); Boca Grande, Gasparilla

Island, Lee Co. (ANSP); Little Gasparilla Island, Lee

Co. (ANSP); 55 m, off Naples, Collier Co. (UF); Naples

Beach, Collier Co. (GTW); Marco Id., Collier Co. (UF);

427 m, 241 km W of Cape Romano, Collier Co. (UF);

Madiera/Pass-a-Grille Beach, Pinellas Co. (UF, UMMZ):

dredged 30 m, Bradenton, Manatee Co. (RV); off Pan-

ama City, Bay Co. (HGL). BAHAMAS: 2-11 m, Cat Cay,

Bimini (UF); Alicetown, Bimini (ANSP); drift, 300 m N

of Current Cut, Current, Eleuthera (HGL); Parrot Cays,

Great Abaco (ANSP); Hog Island (ANSP). CUBA:

(GTW); Matanzas (GTW); Playa del Frances (GTW);

Varadero (ANSP, GTW); 57m, 0.8 km out from bay side

of Icacos Peninsula (ANSP): Tarallones de Arena, near

Santiago (ANSP). PUERTO RICO: (GTW); off Cabo

Rojo Lighthouse (UF); Mayaguez (GTW); Punta Arenas

(ANSP). VIRGIN ISLANDS: Devils Bay, Virgin Gorda

(UF); St. Croix (UF); Water Id. (GTW); St. Thomas

(ANSP). ST. MARTIN: (ANSP). GRENADA: | m, near

Lance aux Epines (HGL); Grand Anse Beach (ANSP);

7-11 m, entrance of St. George Harbour (ANSP); 0.3-

1 m, Prickly Bay (ANSP). MARTINIQUE: (ANSP, UF,

UMMZ). ARUBA: (GTW). HONDUBAS: 8 m, ESE of

Punta Negro (ANSP); 8 m, N of Man of War Cay

(ANSP); Hopkins, Commerce Bight (ANSP). BRAZIL:

3-6 m, off Clube Iate, Salvador, Bahia State (HGL); 1-

3 m, Salvador, Bahia State (HGL):; 9-10 m, Porto Belo,

Santa Catarina State (HGL).

Distribution: Subtidal to at least 90 m. Western At-

lantic Ocean from South Carolina to southern Brazil,

Gulf of Mexico, Yucatan (Vokes and Vokes, 1983), Ber-

Page 122

muda, and Caribbean Sea. Not recorded from the east-

ern Atlantic Ocean.

Remarks: Lister's (1685) figure 179 and description of

the shell as “slightly purple” identifies it as Papyridea

lata as no purple P. soleniformis are known to the writer.

The rib count of the illustrated specimen is at the min-

imum for P. soleniformis, but only three less than the

minimum for P. lata. Reliance on accurate rib counts for

identification from a 17‘ century picture book may be

unrealistic. The color pattern also suggests P. lata more

so than P. soleniformis. This is the first mention of this

species in the literature (Figure 2). Meuschen (1787)

listed this taxon under the name “Coeur spinosum,”

based on this figure and that of Knorr (1772), but

Meuschen’s work is non-binominal. Knorr (1772) illus-

trated a shell that may refer to one of the two taxa dis-

cussed here, but the figure is too crude for accurate

identification (Figure 3). Knorr’s works also are non-bi-

nominal. Born (1778) cited Knorr’s 1772 illustration, but

did so with a question mark, in describing specimens in

the collection of the Empress Maria Theresa as Cardium

latum. Born redescribed this species with his own figure

in 1780 (Figure 4). This was the first available name for

this species: Cardiwm latum Born, 1778. Voskuil and On-

verwagt (1991) and Kafanov (1997) also reached this

conclusion, but included both P. lata and P. soleniformis

under that name. Finally, Brauer (1878), working with

Born’s types, identified ge with Meuschen’s spinos-

um.

Papyridea lata differs conchologically from P. soleni-

formis in several ways. The former is noticeably more

equilateral and lacks the angulation on the umbones.

The ribs on the posterior half of the shell of P. lata are

flattened, while those of P. soleniformis are triangular.

The scales on the posterior primary ribs are positioned

in a narrow medial band in P. lata, but in P. soleniformis,

they are situated on the postero-dorsal slope of the ribs.

The consistent color pattern of P. soleniformis is rarely

duplicated in the much more variable and brightly col-

ored P. lata. Papyridea soleniformis grows to a larger size

than P. lata.

Papyridea soleniformis (Bruguiére, 1789)

(Figures 5, 6, 14-21)

Chama H. inaequilatera, oblique striata, margine interno den-

tata, ex candido and roseo variegata and fasciata Gualtieri,

1742: pl. 85, fig. H [pre-Linnean; type figure of “Coeur

hiatus” Meuschen, 1787, by original designation].

Solen bullatus Linnaeus —C Inenamnitez, 1782: 66, pl. 6, figs. 49,

50 [rejected work; type figure of Cardium soleniforme

Bruguiére, 1789, herein selected] [reproduced Richard-

son, Abbott and Davis, 1979]; Gmelin, 1791: 3226; Bosc,

1802:13; Dillwyn, 1817: 69 [all non Linnaeus, 1758].

Coeur hiatus Meuschen, 1787: 442 [non-binominal].

Cardium soleniforme Bruguiére, 1789: 235; Bosc, 1802:107.

Cardium bullatum (Linnaeus). Lannea 1819: 6; Anton,

1839: 11; Sowerby, 1841: 2; Reeve, 1845: pl. 2, fig. 8;

Reibisch, 1865: 126 [all non a ILA. 1758].

Cardium bullatum “Lamarck”.—Dunker, 1853: 51.

THE NAUTILUS, Vol. 116, No. 4

Papyridea spinosa (Meuschen)—Adams and Adams, 1858:

456.

Papyridea (Fulvia) bullata (Linnaeus)—Chenu, 1862: 109,

figs. 500-502 [non Linnaeus, 1758].

Cardium (Fulvia) bullata (Linnaeus)—Tryon, 1894: 193, 437,

pl. 116, fig. 78 [non Linnaeus, 1758].

Cardium (Papyridea) spinosum var. Turtoni Dall, 1900b:1108;

Schuchert et al., 1905:132; Boss et al., 1968: 328 [non

Cardium turtoni Sowerby (IL), 1894 = Parvicardium tur-

toni (Sowerby {II}, 1894)].

Cardium bullatum “Chemnitz’.—Lamy, 1941: 462-463 [par-

tim).

Papyridea hiatus |partim] Clench and Smith, 1944: 17.

Papyridea bullata “Chemnitz” —Nicklés, 1950: 170.

Papyridea hiatus (Meuschen).—McLean, 1951: 71, pl. 15, fig.

1 [partim].

Papyridea soleniformis (Bruguiére).—Abbott, 1954: 398 [par-

tim] [not pl. 39n = Papyridea lata (Born, 1778)]; Abbott,

1974: 484 [partim|] [not pl. 22, fig. 5555 = Papyridea lata

(Born, 1778)]; Keen, 1980: pl. 6, fig. 11 [partim]; Abbott

and Dance, 1982: 329, text figure; Voskuil and Onverwagt,

1989: 63, 64, figs. 2.1, 2.1.01, pl. 3, fig. 1; Vermeij and

Rosenberg, 1993: 185, 194.

Papyridea (Papyridea) soleniforme (Bruguiére).—Fischer-Piet-

te, 1977:69-70 [partim].

Description: Shell to 60 mm in length, thin but solid,

elongate-oval, compressed, slightly opisthogyrate, ine-

quilateral, with the umbo located 26-33% back from the

anterior margin. Posterior of umbones angled with a

ridge. Shells gaping antero-ventrally and postero-dorsal-

ly, forming pedal and siphonal gapes respectively. Exte-

rior of shell ornamented with 40-48 primary radial ribs,

equal in width to the inter-rib spaces anteriorly, becom-

ing wider than inter-rib spaces posteriorly. Postero-dor-

sal margin dentate. There is a tendency to form second-

ary ribs posteriorly, particularly along the dorsal side of

the primary ribs. Primary ribs triangular in cross-section.

Anterior-most primary ~ 16 ribs and posterior-most ~ 14

ribs usually ornamented with minute concave scales.

Seales cross entire rib on anterior ribs, but are situated

on the postero-dorsal side on the posterior ribs. Exterior

color consistent on all specimens seen, with white or

yellowish background marked with irregular, inter-

spersed rose or purple blotches and flecks that may form

vague concentric bands. Some specimens have one or

two well-defined, broad rays radiating from the umbones

of the same color. These rarely persist on the exterior

on specimens past 20 mm. Living and freshly dead spec-

imens have a thin, tan-colored periostracum around the

shell margin. Hinge occupying less than 1/2 of total

length. Anterior and posterior lateral teeth of equal size.

Left laterals small, short, and blade-like. Right laterals

slightly larger. Otherwise, lateral teeth and ligament as

in P. lata. Interior of shell white, with exterior colors

showing through. Preserved examples have not been

seen.

Type material: Cardium soleniforme Bruguiére,

1789: Lectotype illustrations, herein selected, Chemnitz,

1782: 65, pl. 6, figs. 49, 50 (see ICZN, 1999: Art. 74.4)

(Figure 6). Cardium (Papyridea) spinosum var. turtoni

G. T. Watters, 2002

Dall, 1900: Syntypes USNM [USGS] 157547, one whole

valve, one fragment (figs. 14, 15).

Type locality: Cardium soleniforme Bruguiére, 1789,

based herein on Chemnitz, 1782: unknown. Cardium

(Papyridea) spinosum var. turtoni Dall, 1900: [Pleisto-

cene]| of Caloosahatchee River, Florida.

Material examined: BERMUDA: 1.5-3.0 m, Coney

Island (GTW, HGL). FLORIDA [Atlantic Ocean]: Palm

Beach Co. (UF); 27 m, N of Dodge Estate, Palm Beach

Inlet, Palm Brach Co. (UF); 36-46 m, Dodge Estate,

Palm Beach Inlet, Palm Brach Co. (UF); Lake Worth,

Palm Beach Co. (ANSP, UF): off Breakers Hotel, Palm

Beach, Palm Beach Co. (UF); off radio tower, Palm

Beach, Palm Beach Co. (UF); 1 m, Bear Cut, Key Bis-

cayne, Dade Co. (GTW, UF); Stiltsville Finger Chan-

nels, Dade Co. (HGL, RV, UF); Newfound Harbor

Keys, Monroe Co. (UF); Middle Sambo Shoals, Key

West, Monroe Co. (UF); off Key West, Monroe Co.

(HGL); Fort Jefferson, Garden Key, Dry Tortugas (UF);

1.2 m, 0.27 km S of Fort Jefferson, Garden Key, Dry

Tortugas (UF); 1.6 km S of Garden Key, Dry Tortugas

(UF); 0-68 m, Dry Tortugas (ANSP). [Gulf of Mexico]:

off Tarpon Springs, Pinellas Co. (UF); Little Sarasota

Bay (ANSP). BAHAMAS: 20 m, off reef NE of North

Point, Great Abaco (ANSP); Grunt Drop, Bimini La-

goon, Bimini (ANSP). PUERTO RICO: Mayaguez

(GTW); off Cabo Rojo Lighthouse (UF). VIRGIN IS-

LANDS: (ANSP); Water Id. (GTW); Honeymoon Bay,

St. Thomas (UF): St. Thomas (ANSP). LESSER AN-

TILLES: 1 m, S side of Long Point, Grenada (ANSP):

7 m, Martinique (ANSP, RV). VENEZUELA: Santa Fé

(RV). BRAZIL: 3-6 m, off Clube Iate, Salvador, Bahia

State (HGL); 1-3 m, Salvador, Bahia State (HGL). SAO

TOME: (ANSP). CAPE VERDE ISLANDS: (ANSP).

ST. HELENA: (USNM).

Distribution: Subtidal to at least 46 m. Western At-

lantic Ocean and Gulf of Mexico from central Florida to

at least Bafa de Todos os Santos, Brazil: Bermuda; Ca-

ribbean Sea from Cuba to Venezuela. Eastern Atlantic

Ocean from Angola (Voskuil and Onverwagt, 1989), As-

cension Island (Packer, 1968), St. Helena (Smith, 1890:

Dall, 1900b), St. Vincent (Dall, 1900b), Sao Tomé, and

Cape Verde Islands. Pleistocene of Florida.

Remarks: In 1787, Meuschen described ”Coeur hia-

tus” based on Gualtieri’s work (1742: plate 85, figure H),

which probably depicts this species (Figure 5). I base

this conclusion on the characteristic color pattern of

small, separated spots found in P. soleniformis. Other

aspects of the figure suggest P. lata, but overall I believe

the figure is closer to P. soleniformis. Meuschen also de-

scribed “Coeur spinosum,” from two figures, one of

which (Knorr) is unidentifiable. The other figure (Lister)

clearly is P. lata. Meuschen thus was the first worker to

recognize that these were two different taxa. Unfortu-

nately, his work was non-binominal, and subsequent use

of them by later authors obliterated his original insight.

The name hiatus remained unused until resurrected by

Page 123

Clench and Smith (1944), who believed they had un-

covered the earliest name for this taxon. Because a non-

binominal rejected name does not enter into homonymy

(ICZN, 1999: Arts. 11.4, 54.2), their illustration and de-

scription resulted in their authorship of the name Pa-

pyridea hiatus. Their concept included both taxa rec-

ognized here, but fortunately earlier names are available

for both species. A similar situation exists for Adams's

and Adams’s 1858 authorship of spinosum. Because Ad-

ams and Adams introduced the species name in Papyr-

idea, there is no conflict with the common Cardium spi-

nosum Lightfoot, 1786 [| = Acanthocardia spinosa].

Clench and Smith (1944) also (Pinadvertently) restricted

Meuschen’s Coeur spinosum to Lister's figure.

Chemnitz (1782) illustrated this species as Linnaeus’s

Solen bullatus (Figure 6), but this work is non-binominal

and rejected. In 1789 Bruguiére described Cardium so-

leniforme based on a list of illustrations that included

both taxa, giving a description sufficiently vague as to

apply to either species. The name was largely ignored

until its use by Keen (1937). It gained immediate pop-

ularity with Abbott's use in the 1954 edition of American

Seashells, and now it is the most widely used of the sev-

eral names applied to these species. However, that

name, as used by Bruguiére and later authors, encom-

passed two species. I hereby restrict the type figure of

Cardium soleniforme to Chemnitz, 1782, pl. 6, figs. 49,

50 (ICZN, 1999: Art. 74.4), which is clearly identifiable

as the species discussed here (Figure 6). This enables

this widely used name to continue to be applied to only

one of the two taxa.

Dall (1900b) introduced this species as Cardium spi-

nosum variety turtoni, despite the earlier name Cardium

turtoni Sowerby (II), 1894. Because varieties proposed

before 1961 are considered to be of subspecific rank

(ICZN, 1999: Art. 45.6.4), and species and subspecies

names may compete as homonyms, Dall’s name is a ju-

nior homonym. Dall’s species was described from the

“Pliocene” of the Caloosahatchee River, Florida, now be-

lieved to be Pleistocene in age.

Kafanoy (1997) placed Cardiwm hiulcum Reeve, 1845,

as a synonym of P. lata (his concept contained both P

lata and P. soleniformis). I have not seen Reeve’s unlo-

calized specimen but it seems closest to P- mantaensis

Olsson, 1961, as suggested by Voskuil and Onverwagt

(1991). Both P. lata and P. soleniformis have cognates in

the eastern Pacific Ocean, indicating a Tethyian distri-

bution for their common ancestors. Papyridea crokeri

Strong and Hertlein, 1937, is the homologue of P. lata,

and P. aspersa (Sowerby, 1833) is the homologue of P

soleniformis.

See under Papyridea lata for comments on identifying

P. lata and P. soleniformis.

UNIDENTIFIED NAMES AND

MISIDENTIFICATIONS

Many references cannot be paired with one or the other

species, as evidenced from the following references to

P. lata and P. soleniformis as defined here.

Page 124

non Rumphius, 1705:pl. 44, fig. N [ = an arcid.?].

non Solen bullatus Linnaeus, 1758: 673; Hanley, 1855: 31, 32

[ = nomen dubium, fide Dodge, 1952].

non Cardium spinosum Lightfoot, 1786. [| = Acanthocardia

spinosa (Lighfoot, 1786)].

non Cardium latum “Born”.—Bruguiére, 1789: 234 [partim|;

Gmelin, 1791: 3255: Bosc, 1802: 106; Link, 1807: 151;

Wood, 1815: 236; Dillwyn, 1817: 125; Lamarck, 1819:13;

Wood, 1825: 27 [all based on Chemnitz, 1782:pl. 19, figs.

192-193 = ? Maoricardium pseudolatum Voskuil and On-

verwagt, 1991].

non Cardium latum “Gmelin”. —Réding, 1798: 190 [based on

Chemnitz, 1782: pl. 19, figs. 192-193 = ? Maoricardium

pseudolatum Voskuil and Onverwagt, 1991].

non Cardium latum “Born”.—Reeve, 1845: pl. 6, fig. 21 [ =

Maoricardium setosum (Redfield, 1846)].

non Cardium (Papyridea) bullatum (Linnaeus).—Herrman-

nsen, 1849:200 [ = nomen dubium, fide Dodge, 1952].

non Afrocardium latum “Born” .—Kirtisinghe, 1978: 28, pl. 11,

fig. 12 [ = Maoricardium pseudolatum Voskuil and On-

verwagt, 1991, fide Voskuil and Onverwagt, 1991].

non Plagiocardium (Maoricardium) latum “Born”. —Lamprell

and Whitehead, 1983: 8 | = Maoricardium pseudolatum

Voskuil and Onverwagt, 1991, fide Voskuil and Onverwagt,

1991].

? Anomalocardia, que pectunculus tenuis pellucidus, leviter

purpurascens Listeri, in latum oblique expansus vertice

obtuso Klein, 1753: 144 [rejected work].

? Blasenarrige Herz Knorr, 1772: 15, pl. 7, fig. 6; also as Coeur

enflé in Knorr, 1773 and Blaasagtig Hart in Knorr, 1775

[rejected work].

? Cardium soleniforme “Bosc” —Schumacher, 1817: 159.

? Cardium bullatum (Linnaeus).—d Orbigny, 1842: 337; Han-

ley, 1843: 130-131; Potiez and Michaud, 1844: 184-185;

Conrad, 1846: 393; Beau, 1853:415; Carpenter, 1857: 364.

? Fulvia bullata (Linnaeus)—Adams and Adams, 1858: 457.

? Cardium spinosum Meuschen.—Krebs, 1864: 116; Krebs in

Clench et al., 1947: 29.

? Cardium bullatum “Lamarck”. —Schramm, 1869: 21: Bordaz,

1899: 182.

? Papyridea bullata (Linnaeus).—Tryon, 1872: 267; Dall, 1889:

54; Marche-Marchad, 1958: 50.

? Papyridea soleniforme (Bruguiére)—Tryon, 1872: 26; Olsson

and McGinty, 1958: 21; Vokes, 1977: 164-165, 168.

? Papyridea spinosum (Meuschen).—Tryon, 1872: 26; Johnson,

1934: 46: McLean, 1936: 118.

? Cardium (Papyridea) bullatum “((Linn.?) Chemnitz)”. —

Smith, 1885: 161-162.

? Cardium (Papyridea) spinosum (Meuschen).—Arango, 1887:

259: Dall, 1900a: 387: “M.B.W,” 1901; 9-10.

? Cardium aff. papyraceum “Chemnitz” —Lorié, 1887: 125.

? Cardium (Papyridea) bullatum (Linné).—Smith, 1890: 302—

303; Dautzenberg, 1900: 245.

? Cardium (Fulvia) bullatum (Linné)—Cockerell, 1894: 105.

? Cardium (Fulvia) apertum.—Cockerell, 1894: 105 [non

Chemnitz, 1782 (non-binominal), nec Lightfoot, 1786 (no-

men nudum), nec Bruguiére, 1789, nec Bosc, 1801).

? Cardium spinosum (Meuschen).—Anonymous, 1901: 106.

? Cardium (Papyridea) spinosum (Meuschen).—Dall and

Simpson, 1902: 489.

? Papyridea soleniformis (Bruguiére)—Tomlin and Shackle-

ford, 1915: 273; Parker, 1956: 309; Parker and Curray,

1956: 2434: Nowell-Usticke, 1959: 13; Olsson, 1961: 250:

Arnow, St. Clair and Arnow, 1963: 170: Matthews and

THE NAUTILUS, Vol. 116, No. 4

Rios, 1967: 118; Kempf and Matthews, 1968: 90; de Jong

and Kristensen, 1968: 23; Rios and Oleiro, 1968: 22-23:

Hoerle, 1970: 58 [Lower Pleistocene]; Rosewater, 1975:

33-34; Treece, 1980: 565; Turgeon et al., 1988: 39; Tur-

geon et al., 1998: 42.

? Papyridea spinosa (Meuschen).—Clench and McClean,

1937: 39; Morretes, 1949: 34.

? Papyridea hiatus (Meuschen).—Aguayo and Jaume, 1947:

No. 21; Poirier, 1952: 28; Morretes, 1954: 41; Coomans,

1963: 170.

? Papyridea spinosum (Meuschen).—Baker, 1950: 124.

>? Papyridea (Papyridea) spinosum.—Haas, 1953: 203.

? Papyridae [sic] soleniformis (Bruguiére).—Porter and Wolfe,

1971: 100.

ACKNOWLEDGMENTS

The author thanks: R. Voskuil, Delft, The Netherlands,

for commenting on an early version of the manuscript

and contributing locality records and photographs of the

Born types; R. Petit, South Carolina, USA, for supplying

copies of invaluable literature; and the staffs of the Uni-

versity of Michigan Museum of Zoology, USA, and Flor-

ida Museum of Natural History, USA, for use of their

collections and libraries. The Academy of Natural Sci-

ences of Philadelphia, USA, and the National Museum

of Natural History, Washington, D.C., USA, loaned im-

portant material and type specimens. H. G. Lee, Florida,

USA, loaned material and made valuable comments on

the manuscript. The comments of G. Rosenberg (ANSP)

and an anonymous reviewer greatly improved the man-

uscript. The conclusions reached here are strictly my

own.

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THE NAUTILUS 116(4):129-131, 2002

Page 129

A new Trigonostoma (Neogastropoda: Cancellariidae) from

Mozambique

Richard E. Petit

M. G. Harasewych

Department of Systematic Biology

National Museum of Natural History

Smithsonian Institution

Washington, D.C. 20560-0118 USA

ABSTRACT

Trigonostoma mozambicense is described from the outer con-

tinental shelf off southern Mozambique. This new species is

readily distinguished from its congeners by its combination of

small adult size, its thick shell with coarsely fenestrated surface

sculpture, a narrow umbilicus lined with spiral cords, as well

as the presence of strong but shallow apertural lirae between

the suture and shoulder, and along the outer lip. This new

species is provisionally assigned to the genus Trigonostoma

based on characters traditionally used to define the genus,

while its affinity to a western African species that has been

included in the genus Scalptia is also recognized.

Additional key words: Indian Ocean, Gastropoda Scalptia.

INTRODUCTION

The Cancellariidae is a family of diverse, highly special-

ized, suctorial gastropods that inhabit soft-bottom, sub-

tidal to bathyal habitats throughout tropical and tem-

perate seas. The shallow-water Cancellariidae of Moz-

ambique were monographed by Petit (1980). The South

African representatives of the family were reviewed by

Barnard (1959) and Kensley (1973) and in recent pop-

ular works by Richards (1981) and Steyn and Lussi

(1998). Several additional species were added to the

South African fauna in papers by Petit and Harasewych

(1991, 2000a, 2000b). Increased biological sampling

along outer continental shelf and upper slope depths

continues to bring to light previously unknown biota.

Over the past year, the Amorim family has kindly made

available specimens of newly discovered gastropods from

off Mozambique (e.g. Harasewych and Fraussen, 2001),

among them the new species of cancellariid described

herein.

SYSTEMATICS

Family Cancellariidae Forbes and Hanley, 1851

Genus Trigonostoma Blainville, 1827

Type Species: Delphinula trigonostoma Lamarck,

1822 (?= Buccinum scalare Gmelin, 1791) by monotypy.

Trigonostoma mozambicense new species

(Figures 1-6)

Diagnosis: A small species with a thick, broadly tab-

ulate, narrowly umbilicate shell with strong, scabrous ax-

ial ribs and spiral cords that produce a fenestrated sur-

face sculpture. Umbilicus lined with spiral cords. Outer

lip with strong, short lirae between suture and shoulder

as well as between shoulder and siphonal canal.

Description: Shell (Figures 1-2) small, reaching 16.1

mm, heavy, ovately biconical, strongly shouldered, with

deep, narrow umbilicus. Spire relatively short (spire an-

gle 83°), comprising just over half the shell length. Pro-

toconch (Figures 4-5) increasing in diameter from 0.52

mm to 1.38 mm in 1% smooth, inflated, slightly cylin-

drical whorls. Transition to teleoconch sharply demar-

cated by onset of spiral cords and numerous, fine, axial,

growth lamellae, followed within % whorl by axial ribs.

Teleoconch with up to 3% sharply angled whorls. Suture

weakly impressed on first two teleoconch whorls, abut-

ting to weakly adpressed on last whorl. Axial sculpture

of sharp, prosocline ribs (14-17 on penultimate whorl)

that become less numerous (8-12), and progressively

broader, more widely spaced and more scabrous on last

whorl, producing distinctive, fenestrated surface sculp-

ture. Spiral sculpture consists of strong cords (Figure 6,

C) and primary (Figure 6, p), secondary (Figure 6, s)

and tertiary (Figure 6, t) threads that overlay both cords

and intervening spaces. Spiral cords are absent on tab-

ulate shoulder, 3 cords present from periphery to suture,

6 cords on last whorl, cords strongest on periphery and

siphonal fasciole. Aperture sharply triangular, offset from

shell axis by 18°. Siphonal canal short, well defined,

slightly deflected dorsally. Outer lip thick, weakly flared,

crenulated beneath spiral cords, with 3 strong, shallow

teeth along the tabulate region of the whorl (evident

only in holotype) and 9 strong teeth along outer lip, be-

neath last axial rib (varix). Varices and spiral cords de-

marcate uniquely translucent regions within outer lip

(Figure 3, arrows). Short parietal region forms an angle

of 130° with long, straight columella that bears 2 strong

Page 130 THE NAUTILUS, Vol. 116, No. 4

Figures 1-6. Trigonostoma mozambicense new species. Collected by fishing boats south of Bazaruto and north of Maputo,

Mozambique, in 100-150 m. 1. Apertural, right lateral, and dorsal views of holotype, USNM 1007053. 2. Apical view of holotype.

3. Aperture of holotype, oblique view showing translucent areas (arrows). 4. Apical and 5. Oblique view of protoconch of holotype.

6. Detail of spiral sculpture. Abbreviations: c, cords; p, primary threads; s, secondary threads; t, tertiary threads. Scale bar (3 mm)

applies to all whole shells.

R. E. Petit and M. G. Harasewych, 2002

columellar folds near mid-length and a nearly indiscern-

ible siphonal fold. A short parietal callus spans the in-

ductural region. Umbilicus, deep, narrow, spiral cords

within, well defined by thick, prominent siphonal fasci-

ole. Shell base color light brown, maculated with dark

brown patches between axial cords, especially on tabled

shoulder near suture and/or periphery. Protoconch and

early whorls pinkish brown. Radula and anatomy un-

known.

Type locality: South of Bazaruto and north of Ma-

puto, Mozambique, in 100-150 m.

Material examined: Holotype (National Museum of

Natural History, Smithsonian Institution, USNM

1007053); paratype 1 (Natal Museum, Pietermaritzburg,

L5749/T1917), Paratypes 2-3, Amorim collection. All col-

lected by fishing boats based in Maputo, Mozambique,

March 2001, from the type locality; paratype 4, Brink Col-

lection, off Quissico/Zavora, Mozambique, in fish trap at

120-150 m, December 2001, collected by José Rosado;

Paratype 5, Petit Collection #2724, off Quissico/Zavora,

Mozambique, in fish trap at 120-150 m.

Remarks: This new species most closely resembles

the west African Scalptia scala (Gmelin, 1791) [often

listed under its junior synonym Scalptia withrowi (Petit,

1976)], as well as the Panamic species Trigonostoma

goniostoma (Sowerby, 1832) and Trigonostoma breve

(Sowerby, 1832) in general shell morphology, and in

sharing several unusual shell characters, among them: a

tabulate shell that is pigmented near the suture, the

presence of denticles under the sutural ramp, a strongly

defined siphonal fasciole, and the presence of strong

cords within the umbilicus. Trigonostoma mozambicense

may be readily distinguished from S. scala on the basis

of its smaller shell, its broader, more scabrous axial

sculpture, in having fewer, stronger and shallower ap-

ertural lirae, and in having two columellar folds rather

than three folds of S. scala. Scalptia scala has fine pus-

tules or denticles along the columella, which are lacking

in I. mozambicense. Like Trigonostoma goniostoma and

T. breve, T. mozambicense has two columellar folds.

However, it can readily be distinguished from both Pan-

amic species by its smaller shell size, its more rounded

whorls, its rounded periphery, and by having broader,

more scabrous axial ribs.

While this new species is readily distinguished from

other cancellariids on the basis of its shell morphology,

there is some question as to its correct generic place-

ment. The species with which it is compared appear to

comprise a coherent group. Additional material and fur-

ther study will be required to confirm the monophyly of

Page 131

this group, to define more precisely the limits and re-

lationships of the genera Trigonostoma and Scalptia, and

to determine the relationship of this group to these gen-

era. Over a century ago Cossmann (1899: 16) discussed

the differences between Scalptia and Trigonostoma and

assigned these genera to different subfamilies.

We provisionally include this new species in Trigo-

nostoma as it shares a number of features that have heen

used to diagnose Trigonostoma (e.g., two columellar

folds, a straight colina, an Henle)!

ACKNOWLEDGMENTS

We are grateful to the Amorim family (Mozambique and

Portugal) for bringing this species to our attention, and

for providing the much of the type material. Thanks are

due to Dawn Brink of South Africa for obtaining and

making additional specimens available for study.

LITERATURE CITED

Barnard, K. H. 1959. Contributions to the knowledge of South

African marine Mollusca. Part II. Gastropoda: Prosobran-

chiata: Rhachiglossa. Annals of the South African Museum

45: 1-237.

Gmelin, J. F. 1791. Caroli a Linné Systema Naturae per regna

tria naturae. Editio decima tertia. Vol. 1, pt. 6 (Vermes)

Lipsiae, pp. 3021-3910.

Harasewych, M. G. and K. Fraussen. 2001. Coluzea groschi, a

new species of Columbariinae (Gastropoda: Turbinellidae)

from Southeastern Africa. Novapex 2: 171-174.

Kilburn, R. and E. Rippey. 1982. Sea Shells of Southem Africa.

Macmillan South Africa, Johannesburg, xi + 249 pp.

Petit, R. E. 1976. Notes on Cancellariidae (Mollusca: Gastro-

poda)—HI. Tulane Studies in Geology and Paleontology

12: 33-43, pls. 1-2.

Petit, R. E. 1980. The Mozambique Cancellariidae (Mollusca:

Gastropoda). Annals of the Natal Museum 24; 211-216.

Petit, R. E. and M. G. Harasewych. 2000a. Additions to the

cancellariid (Mollusca: Neogastropoda) fauna of South Af-

rica. Proceedings of the Biological Society of Washington

113: 145-154.

Petit, R. E. and M. G. Harasewych. 2000b. Three new species

of the genus Merica (Neogastropoda: Cancellariidae) from

South Africa and the Philippines. The Nautilus 114: 142—

148.

Richards, D. 1981. South African Shells. A collector's guide. C.

Struik, Cape Town, 98 pp., 60 pls.

Sowerby, G. B., I. 1832. Genus Cancellaria. In: W. J. Broderip

and G. B. Sowerby, Characters of new species of Mollusca

and Conchifera, collected by Mr. Cuming. Proceedings of

the Zoological Society of London for 1832: 50-55.

Steyn, D. G. and M. Lussi. 1998. Marine Shells of South Af

rica. Ekogilde, Hartbeespoort, South Africa, 264 pp.

THE NAUTILUS 116(4):132-137, 2002

Page NBy

Samuel Liberty Harvey Fuller (1942-2001): a biographical

sketch and his works on malacology

Richard I. Johnson

Department of Malacology!

Museum of Comparative Zoology

Harvard University

Cambridge, MA 02138 USA

ABSTRACT

This article lists all of Samuel Liberty Harvey Fuller’s almost

. . » . 4 . oe

60 publications, most of which treat Unionoidea. Fuller de-

scribed a new molluscan taxon, Elliptio marsupiobesa, in 1972.

Additional key words: new species, taxonomy, biogeography,

North America.

Samuel (Sam) Liberty Harvey Fuller was born on March

2, 1942, the first son of Alan Henry and Vera Harvey

nile He spent his childhood on land that had been

farmed by his family for four generations. The Fullers

were amongst the earliest eenlens of Suffield, Connect-

icut, where ‘they persist in some numbers to this day and

have long been prominent in the affairs of Suffield Acad-

emy. During Fuller's youth his father was forced to give

up tobacco growing because of a new dev elopment in

the manufacture a cigar wr appers to become a teacher

of mathematics at Suffield Academy, Suffield, Connect-

icut. Sam's early penchant for natural history was en-

couraged by his parents who took him on Saturdays to

Springfield, Massachusetts. There he spent mornings at

the YMCA and afternoons at the Springfield Neder

History Museum. He became a role model for his three

younger siblings, Henry, Woodbridge (Woody), and a sis-

ter, Tamsen. Woody Fuller, who spent hours with his

brother searching ‘for freshwater mussels along the

Windsor Locks Camel called Sam a “curiosity mentor

and a natural teacher. He helped me to be curious about

the world. He was good at stimulating interest in other

people.”

A brilliant student at Wooster, Sam was one of the

few who graduated with a “6 average,” its most superior

grade. He achieved perfect SAT scores and became, I

Beliene. the first of his branch in a long line of Fullers

in America to attend Harvard College, where he enjoyed

a Harvard National Scholarship (1960-1963). In his first

letter to the Museum of Comparative Zoology, dated

' Associate in Malacology

March 26, 1958, Sam begins, “Dear Sirs: I am sending

to your department several varieties of freshwater mol-

lusk which I hope you might identify for me.” This was

the beginning of a beautiful friendship with Curator Wil-

liam J. Clench that lasted until Clench’s death in 1984.

Sam spent much time during his undergraduate years at

the Department of Mollusks, where he would usually

appear as a tatterdemalion. He dressed as a gentleman

only when he set off to Roxbury to tutor underprivileged

children. He spent the month of August and some of

September 1961 collecting in the rivers of Georgia with

Clench and Kenneth Jay Boss, who would later succeed

Clench as Curator of Mollusks. Early in the trip, while

on the quest for large Elliptio hopetonensis, at the first

really successful collecting site in the Altamaha River,

Boss rescued Sam from almost certain drowning.

The following summer, Sam joined me, my wife, and

two small daughters on an “expedition”, as we called it,

to peninsular Florida to collect freshwater mussels. He

was an excellent babysitter, able to keep the girls

amused, and a fine field collector. We made 49 success-

ful collecting stops. He humored my then wife when she

tried to help interpret our county maps her way. They

were able to establish distant kinship through Stephen

Fuller Austin, the Texan hero of the Alamo ae had also

been born in Suffield, Connecticut. It was Sam’s respon-

sibility to navigate whilst one of us drove. He worked on

his life list of birds, and would cry out the name of each

one he sighted which was new to him. In the evenings

after the last shell had been cleaned, he would practice

on his guitar, for which he had no talent, or else read

avidly the works of William Faulkner or novels such as

Steppenwolf and Demian by Herman Hesse. Before the

summer was over, I was also reading these books and

discussing them with Sam. In 1964, upon graduating

from ered with a degree in biology, Sam received a

Ford Foundation grant and went to Tanzania for a year

as an instructor at the Kurasini International College. He

left behind June, the Radcliffe junior he intended to

marry, to complete her undergraduate studies.

Sam had several narrow escapes in Africa, one of

which was an attack by a swarm of killer bees. Through

R. IL. Johnson, 2002

his own accounts and by my observations Sam was ac-

cident-prone. In an amusing 1971 article, one of several

Sam wrote for the Academyss popular publication, Fron-

tiers, he relates, “I picked my way across Old Brown’s

yard, knocked, and tripped flat on my face into the kitch-

en.” I had planned another trip to the South for him

when he returned from Africa, but his commitment to

civil rights, shared by his fiancée whose parents were

social workers, and their determination to collect and

participate in the civil rights movement, led me to cancel

the trip. Those were troubled times in the South and I

insisted that civil rights work, although admirable, could

be done effectively only under the protection of an um-

brella organization.

Upon Sam’s return to the United States, June put off

the wedding because of the recent death of her father.

Eventually, their engagement was dissolved. Sam took a

post teaching at the Wooster School in Danbury, Con-

necticut, from which he had so brilliantly graduated not

many years before. In 1968, Sam wrote to Dr. Clench

informing him that he was to be married to Mary (Micki)

Lou Bush at the Wooster School. Soon after their mar-

riage, Dr. Ruth Patrick of the Department of Limnology

of the Academy of Natural Sciences in Philadelphia

called me about a position to assist in her department.

Since it did not interest me, I recommended Sam, who

I thought to be a perfect candidate. With some trepi-

dation, he accepted Dr. Patrick’s offer. Micki and he set-

tled in New Jersey where they became parents of two

children. A glance at Sam’s bibliography between 1971

and 1981 reveals his impressive contributions to the

study of Unionoidea. Without ever taking a higher de-

gree, he had schooled himself in their anatomy and mo-

lecular genetics. He was also responsible for an extensive

geographic survey of the mussels of the Upper Missis-

sippi River and led symposia on endangered species.

Sam also found time to act as an instructor at Rutgers

University, New Brunswick, New Jersey.

His independent work habits appear eventually to

have caused his severance from the Academy. He re-

turned to Connecticut where the family was in a serious

automobile accident, not of his making, in October 1973.

His son, Samuel, Jr., was killed and his daughter, Re-

becca, seriously injured. A divorce ensued.

In 1990, Sam wrote, “I seem to be back in biology

after seven lean, unwelcome years of sorrow and loss.”

After an absence of a quarter of a century, Sam paid a

visit to the Department of Mollusks at Museum of Com-

parative Zoology when he was on his way to Florida to

work again on his favorite mollusks as Research Associ-

ate with James D. Williams of the National Fisheries

Research Center of the U.S. Fish and Wildlife Service

in Gainesville, Florida. After a few years there, he dis-

appeared from view, only to reappear through the kind-

ness of Mrs. Deborah M. Heath, who saw that he was

comfortably cared for before his death of lung cancer

on April 13, 2001. He had earlier predicted that lung

cancer would get him as it had his father. He and I

carried on a spirited correspondence toward the very

Page 133

end. In his last letter to me from Ocala, Florida, he

mentioned his intention of naming a new species of mus-

sel after me.

Harvard College graduates stage reunions every five

years and publish a volume of autobiographies of class-

mates on each occasion. There seems to be an indication

that those who contribute to Class Reports live longer

than those who do not. It does not follow that the longer

the report, the longer the life. Samuel Liberty Harvey

Fuller never contributed to a Class Report. He was list-

ed as “lost” at the Wooster School until shortly before

his death. He is now listed “In Memoriam” with his Har-

vard Class of 1964.

NEW TAXA INTRODUCED BY SAMUEL LIBERTY

HARVEY FULLER

splendens, Gnathophyllum Chase and Fuller, 1971 (De-

capoda, Caridea). Proceedings of the Biological Society

of Washington (1970) 83: 493-505 (Puerto Yabucoa, 0.5

mi. E Playa de Guayanés, Municipio de Yabucoa, Puerto

Rico; holotype United States National Museum 134422

[only specimen)).

marsupiobesa, Elliptio Fuller, 1972. Proceedings of the

Academy of Natural Sciences of Philadelphia 124(1): 1—

10, pl. 1, fig. 1 (Cape Fear River, 0.1 mile downstream

from Carvers Creek, about 3 miles SW of Slocomb, and

about 6 miles NNE of Fayetteville, Cumberland Co.,

North Carolina). Female holotype Academy of Natural

Sciences of Philadelphia UANDIE) 324501; paratypes Mu-

seum of Comparative Zoology (MCZ) 272780, ANSP

324502(16), 324503(2), 324504(3), 324505(1).

BIBLIOGRAPHY OF SAMUEL LIBERTY HARVEY

FULLER

Fuller, S. L.H. 1965. Untapped Tanzania riches. Nation-

alist, Dar es Salaam, Tanzania, 1 p. [February 4]

Clench, William J. and S. L. H. Fuller. 1965. The genus

Viviparus Wunpanae) in North America. Occasional

Papers on Mollusks 2(32): 385-412, pls. 64-68. [July 9]

Hendrickson, Jr., John A., S. L. H. Fuller and Katherine

B. Roop. 1970. An ecology handbook. Frontiers 34(5):

18-21. [June]

Fuller, S. L. H. 1970. Fuller’s earth. Wooster News,

Wooster School News, Danbury, Connecticut, pp. 4-13.

[Fall Term Issue].

Fuller, S. L. H. 1971. Pond Life [review]. Bulletin of the

Philadelphia Herpetological Society 18: 49.

Chace, Jr., Fenner A. and S. L. H. Fuller. 1971. A new

shrimp of the genus Gnathophyllum (Decapoda, Cari-

dea) from Puerto Rico. Proceedings of the Biological

Society of Washington 83(4): 493-504, text figs. 1-7.

[February 9]

Page 134

Figure 1. Samuel Liberty Harvey Fuller. October, 1973.

Fuller, S. L. H. 1971. Everything you always wanted to

know about freshwater mussels but were afraid to ask.

Frontiers 35(5): [1]2-9. [June]

Fuller, S. L. H. 1971. Fossils and Flies—The life of a

Complete Scientist, Samuel Wendell Williston (1851—

1918) [review] Frontiers 36(1):; 30-31. [October—No-

vember]

Fuller, S. L. H. 1971. A brief field guide to the fresh-

water mussels (Mollusca: Bivalvia: Unionacea) of the Sa-

vannah River system. ABS [Association of Southeastern

Biologists] Bulletin 18(4): 137-146, text figs. 1-14, 1 pl.

Fuller, S. L. H. and C. W. Hart, Jr. 1972. Changes along

the Patuxent. Frontiers 36(3):; 2-7.

Fuller, S. L. H. 1972. Uganda Quest [review]. Frontiers

36(4): 29. [April]

Hart, C. W., Jr., and S. L. H. Fuller. 1972. Environmen-

tal degradation in the Patuxent River Estuary, Maryland.

Contributions from the Department of Limnology Acad-

THE NAUTILUS, Vol. 116, No. 4

emy of Natural Sciences of Philadelphia 1:1-14. [Sep-

tember]

Fuller, S. L. H. 1972. Ecotage! [review] 37(1): 31-32.

[October]

Fuller, S. L. H. 1972. Elliptio marsupiobesa, a new

fresh-water mussel (Mollusca: Bivalvia: Unionidae) from

the Cape Fear River, North Carolina. Proceedings of the

Academy of Natural Sciences of Philadelphia 124: 1-10,

6 figs. [November 24]

Fuller, S. L. H. 1972. Type locality of Unio pumilus Lea,

1838 (Unionidae). The Nautilus 86: 72-73. [November]

Fuller, S. L. H. 1972. Unio caroliniana Bosc, 1801

(Unionidae). The Nautilus 86: 74-75. [November]

Fuller, S. L. H. 1972. An undescribed structural feature

in the marsupium of Elliptio lanceolata (Lea 1828)

(Unionidae): The Nautilus 86: 85—S6. [November]

Powell, Jr, S. L. El. Fuller and) @) W, Wart |relon2

Some advantages and disadvantages of a multiple-plate

conservation webbing artificial substrate as a supplement

to hand collecting of macroinvertebrates in Chesapeake

Bay. ABS [Association of Southeastern Biologists] Bul-

letin 19(2): 92.

Fuller, S. L. H. and Charles E. Powell, Jr. 1973. Range

extensions of Corbicula manilensis (Philippi) in the At-

lantic drainage of the United States. The Nautilus 8: 59.

[April]

Fuller, S. L. H. 1973. The spiny shells of the Altamaha.

Frontiers 37(4): 14-15. [summer]

Fuller, S. L. H. and D. J. Bereza. 1973. Recent additions

to the naiad fauna of the eastern Gulf drainage (Bivalvia:

Unionoidae) (Abstrace). ASB [Association of Southeast-

ern Biologists] Bulletin 20(2): 53-54.

Fuller, S. L. H. 1974. Fusconaia masoni (Conrad 1834)

(Bivalvia: Unionacea) in the Atlantic drainage of the

southeastern United States. Malacological Review 6:

105-117. [January 29]

Fuller, S. L. H. 1974. A misunderstood fresh-water mus-

sel from the Savannah River system in South Carolina

(Bivalvia: Unionidae) (Abstract). ASB [Association of

Southeastern Biologists] Bulletin 21(2): 55-56. [April]

Fuller, S. L. H. 1974. Neglected papers on naiads by W.

I. Utterback. The Nautilus 88: 90. [July 22]

Fuller, S. L. H. 1974. The Life of Captain James Cook

[review]. Frontiers 38(4): 31. [summer]

Fuller, S. L. H. 1974. The journey of the Chinese clam.

Frontiers 39(2): 12-13. [winter]

Fuller, S. L. H. 1974. Biota of Freshwater Ecosystems:

A review. ASB [Association of Southeastern Biologists]

Bulletin 21(3); 109-112.

R. I. Johnson, 2002

Fuller, S. L. H. 1974. Clams and mussels (Mollusca: Biv-

alvia): In: Hart, Jr, C. W. and S. L. H. Fuller (Eds.)

Pollution ecology of freshwater invertebrates. Academic

Press, New York and London. Chapter 8, pp. 215-273.

Fuller, S. L. H. 1974. Macroinvertebrates. In: Savannah

River Biological Survey, South Carolina and Georgia,

May and September, 1972 for I. E. duPont de Nemours

& Co. Department of Limnology and Ecology, Academy

of Natural Sciences of Philadelphia, pp. 56-76, 147-150

[proprietary to I.E. duPont de Nemours & Co.; not

seen].

Fuller, S. L. H. 1974. Macroinvertebrates (and) Quan-

titative macroinvertebrate samples. pp. 49-69, 143-145

[in] Cooper River Survey for 1973 for I. E. duPont de

Nemours & Co. Department of Limnology and Ecology,

Academy of Natural Sciences of Philadelphia [proprie-

tary to I. E. duPont de Nemours & Co.; not seen].

Bereza, D. J. and S. L. H. Fuller. 1975. Notes on Lamp-

silis ochracea (Say) (Mollusca: Bivalvia). (Abstract) ASB

[Association of Southeastern Biologists] Bulletin 22(2):

49.

Fuller, S. L. H. 1975. Fresh-water mussels (Mollusca:

Bivalvia) in the Chowan River system of Virginia. (Ab-

stract). ASB [Association of Southeastern Biologists]

Bulletin 22(2): 54.

Fuller, S. L. H. 1975. The systematic position of Cyr-

tonaias (Bivalvia: Unionidae). Malacological Review 8:

81-89.

Fuller, S. L. H. and D. J. Bereza. 1975. The value of

anatomical characters in naiad taxonomy (Bivalvia:

Unionacea). Bulletin of the American Malacological

Union, 1974: 21-22.

Fuller, S. L. H. 1975. Macroinvertebrates (excluding in-

sects) Appendix B, B-1-B-26 [in] Hendrickson, John A.,

Final report submitted to National Commission on Wa-

ter Quality under Contract No. WQ5ACo44 on selected

segments of the Santee River basin. XI. Biological, eco-

logical, and environmental characteristics of the site. p.

X-1 to XI-69. XIV-1 to XIV-13, A-2 to A-30, B-1 TO B-

26, C-1 to C-17, D-1 to D-15, E = 1 to E-4, F-1 to F-

3, G-1 to G-3, H-1 to H-4. Department of Limnology

Academy of Natural Sciences of Philadelphia. (Subse-

quently distributed by National Technical Information

Service, 5283 Port Royal Road, Springfield, Virginia.

[July]

Bereza, D. J., M. F. Vidrine and S. L. H. Fuller. 1976.

Anatomical differences between Ligwmia nasuta (Say)

and L. swbrostrata (Say). (Abstract) ASB [Association of

Southeastern Biologists] Bulletin 23(2): 43.

Fuller, S. L. H. 1976. Apparent resurgence of Hydroli-

max grisea (Haldeman), the Grizzly Water Slug (Platy-

helminthes: Turbellaria: Alloecoela). ASB [Association of

Southeastern Biologists] Bulletin 23: 60. —

Page 135

Fuller, S. L. H. and M. J. Imlay. 1976. Spatial compe-

tition between Corbicula manilensis (Philippi), the Chi-

nese Clam (Corbiculidae), and fresh-water mussels

(Unionidae) in the Waccamaw River basin in the Caro-

linas (Mollusca: Bivalvia). (Abstract) ASB [Association of

Southeastern Biologists] Bulletin 23(2): 60.

Fuller, S. L. H., M. J. Imlay and James D. Williams.

1976. Endangered or threatened fresh-water mussels

(Mollusca: Bivalvia: Unionidae) of the Waccamaw River

basin of the Carolinas. (Abstract) ASB [Association of

Southeastern Biologists] Bulletin 23(2): 60.

Davis, G. M., S. L. H. Fuller and C. Hesterman. 1977.

Toward a definitive higher classification of North Amer-

ican Unionidae. (Abstract). Bulletin of the American

Malacological Union, Inc. 1977: 85

Fuller, S. L. H. 1977. Freshwater and terrestrial mol-

lusks. In: Cooper, J. E., S. S. Robinson, and J. B. Fun-

derburg (eds.) Endangered and threatened plants and

animals of North Carolina, North Carolina State Muse-

um of Natural History, Raleigh, pp. 143-194.

Fuller, S. L. H. and J.W. Richardson. 1977. Amensalistic

competition between Corbicula manilensis (Philippi),

the Asiatic Clam (Corbiculidae), and freshwater mussels

(Unionidae) in the Savannah River of Georgia and South

Carolina (Mollusca: Bivalvia). (Abstract) ASB [Associa-

tion of Southeastern Biologists] Bulletin 24(2): 52.

Fuller, S. L. H. 1978. Final Report. Fresh-water mussels

(Mollusca: Bivalvia: Unionidae) of the upper Mississippi

River: Observations at selected sites within the 9-foot

channel navigation project on behalf of the United States

Army Corps of Engineers. Report No. 78-33, 401 pp.

Academy of Natural Sciences of Philadelphia. [June]

Fuller, S. L. H. 1978. Corps/Service cooperate to protect

endangered mussels. Endangered Species Technical

Bulletin 3(9): 3-6. Department of the Interior, U. S.

Fish and Wildlife Service. Endangered Species Program,

Washington, D.C. [September]

Fuller, S. L. H. 1978. The changing molluscan com-

munity. pp. 124-131. [in] Flynn, K. C. and W. T. Mason

(Eds.). The freshwater Potomac: aquatic communities

and environmental stresses. Proceedings of a symposium

in January 1977, at College Park, Maryland. Interstate

Commission of the Potomac River Basin, Rockville,

Maryland. pp. 1-194.

Fuller, S. L. H. 1978. Freshwater mollusks, pp. 136-152.

In: Zingmark, R. G. (ed.) An annotated checklist of the

biota of the coastal zone of South Carolina. University

of South Carolina Press, Columbia, South Carolina. pp:

xii, 364.

Davis, G. M., S. L. H. Fuller and C. Hesterman. 1978.

(Abstract) Bulletin of the American Malacological Union

for 1977: 85.

Page 136

Hart, Jr., C. W. and S. L. H. Fuller. 1979. Pollution Ecol-

ogy of Estuarine Invertebrates. New York, Academic

Press [editors only].

Fuller, S. L. H. 1979. Freshwater mussels (Mollusca:

Bivalvia: Unionidae). In: Forsythe, D. M. and W. B.

Ezell, Jr. (eds.) Proceedings of the first South Carolina

endangered species symposium. South Carolina Wildlife

and Marine Resources Department, Columbia. pp. 114—

128.

Fuller, S. L. H., F. W. Grimm, T. L. Laavy, H. J. Porter

and A. H. Shoemaker. 1979. Status Report: Freshwater

and Terrestrial mollusks. In: Forsythe, D. M. and W. B.

Ezell, Jr. (eds.) Proceedings of the first South Carolina

endangered species symposium. South Carolina Wildlife

and Marine Resources Department, Columbia, pp. 55-

59.

Fuller, S. L. H. and Raymond H. Hartenstine. 1980. An-

odonta imbecillis Say (Bivalvia: Unionidae) in the Dela-

ware River Basin. The Nautilus 94: 4. [January 30]

Fuller, S. L. H. 1980. Final Report. Freshwater mussels

(Mollusca: Bivalvia: Unionidae) of the upper Mississippi

River: Observations at selected sites within the 9-foot

navigation channel project for the St. Paul District.

1977-1979. Report No. 9-24F, vol. 1, 175 pp.; vol. 2,

appendices, xiv + 401 pp., Academy of Natural Sciences

of Philadelphia. [September]

Britton, J. C. and S. L. H. Fuller. 1980. The freshwater

bivalve mollusca (Unionidae, Sphaeridae, Corbiculidae)

of the Savannah River Plant, Aiken, South Carolina.

Publication of the Savannah River Plant, National En-

vironmental Research Park Program United States De-

partment of Energy. SRO-NERP-3. pp. 1-37. [Novem-

ber]

Fuller, S. L. H. 1980. Historical and current distribu-

tions of freshwater mussels in the upper Mississippi Riv-

er. pp. 72-119. In: Rasmussen, Jerry L. (ed.) Proceed-

ings of the UMRCC symposium on upper Mississippi

River bivalve Mollusks. Upper Mississippi River Con-

servation Committee, Rock Island, Illinois, 270 pp.

Fuller, S. L. H. 1980. Freshwater mussels of the upper

Mississippi River, 2 pp. [This two-sheet, 30” by 40” post-

er was distributed by the United States Fish and Wildlife

Service and the U. S. Army Corps of Engineers as an

aid to mussel identification] E. Ambrogio and M. Fuges.

[not seen}

Davis, G. M. and S. L. H. Fuller. 1981. Genetic rela-

tionships among Recent Unionacea (Bivalvia) of North

America. Malacologia 20: 217-253 + 2 appendices

Davis, G. M., W. H. Heard, S. L. H. Fuller and C. Hes-

terman. 1981. Molecular genetics and speciation in El-

liptio and its relationships to other taxa of North Amer-

ican Unionidae (Bivalvia). Biological Journal of the Lin-

nean Society 15(2): 131-150.

THE NAUTILUS, Vol. 116, No. 4

Thomas, R. L., and S. L. H. Fuller. 1982. The freshwater

mussel fauna of the Upper Mississippi River near locks

and dam 19 at Keokuk, Iowa (Abstract 119). Abstracts

of Contributed Papers. 94'" session, Iowa Academy of

Science, Fort Dodge, April 16-17, 1982 p.27.

Coney, C., S. L. H. Fuller, G. M. Davis, R. H. Moore,

and J. M. Shipley. 1983. Adaptive radiation and conver-

gence in the Cape Fear River basin Unionidae (Mollus-

ca: Bivalvia). (Abstract). Bulletin of the South Carolina

Academy of Science 45: 87-88.

Fuller, S. L. H. 1985. Freshwater mussels of the upper

Mississippi River. 64 pp. Wisconsin Department of Nat-

ural Resources, Madison, Wisconsin. (Text by S. L. H.

Fuller, Revision by Inga Byrnildson)

Bogan, A. E., J. D. Williams and S. L. H. Fuller. 1990.

Comments on the proposed conservation of Proptera

Rafinesque 1819 (Mollusca: Bivalvia). Bulletin of Zoo-

logical Nomenclature 4: 206-207. Case 2558.

Williams, J. D, S. L. H. Fuller and R. Grace. 1992. Ef

fects of impoundments on freshwater mussels (Mollusca:

Bivalvia: Unionidae) in the main channel of the Black

Warrior and Tombigbee rivers in western Alabama. Al-

abama Museum of Natural History, Bulletin 13: 1-10.

[September 25]

The following titles were referred to by Fuller in: An

annotated checklist of the biota of the coastal zone of

South Carolina (1978), but only abstracts under similar

titles of some of them have appeared.

Fuller, S. L. H. and D. J. Bereza. 1975. A new genus-

group name for Unio ochraceus Say. See: Bereza and S.

L. H. Fuller (Fuller).

Fuller, S. L. H. and M. J. Imlay. 1976. A new genus-

group for Mya radiata (Gmelin, 1791).

Fuller, S. L. H., M. J. Imlay and J. D. Williams. 1976.

Freshwater-mussels (Mollusca: Bivalvia: Unionidae) in

the Waccamaw River Basin of the Carolinas. See: Fuller,

S. L. H., M. J. Imlay and J. D. Williams (1976).

Fuller, S. L. H., R. M. Shelley and M. J. Imlay. 1975.

Fresh-water mussels (Mollusca: Bivalvia: Unionidae) in

the Chowan River Basin of Virginia and North Carolina.

See: Fuller, S. L. H.

ACKNOWLEDGMENTS

All quotations are from letters on file in the Department

of Mollusks at the Museum of Comparative Zoology,

Cambridge, Massachusetts. Some were sent to the De-

partment, others were sent to William J. Clench, at

home, for his eyes-only. Clench left his files to Ruth D.

Turner who in turn left them to the Department. Some

letters were personal to me. Mr. Henry Fuller made cer-

tain corrections to the manuscript regarding details of

his brother's life and kindly supplied the photograph of

him. Neither Mrs. Fuller nor daughter Rebecca deigned

R. I. Johnson, 2002

to reply to several requests for information. Thanks are

also extended to Mr. Daniel Elliott, Librarian of the Ew-

ell Sale Stewart and Dr. Daniel L. Graf, Assistant Cu-

rator of Malacology of the Academy of Natural Sciences

of Philadelphia, Ms. Susan DeSanctis, Ms. Mary B. Sears

and Mr. Ronnie Broadfoot of the Ermmst Mayr Library of

the Museum of Comparative Zoology for locating and

making available some of the works referred to.

Page 137

ADDITIONAL LITERATURE CONSULTED

Abbott, R. T. 1973. American Malacologists. American Mala-

cologists, Falls Church, 494 pp.

Hamilton, A. M. 2001. Fascination with mollusks led to a bril-

liant career. Hartford (Connecticut) Courant. p. H2. (A

fitting encomium). [Sunday, October 2]

Page 138 THE NAUTILUS, Vol. 116, No. 4

Erratum

In the article by Bouchet and Petit (2002), on page 100, under the “Remarks” section for the species Merica marisca,

please replace the word pirum for marisca. The word pirum should have no nomenclatural standing within the context

of that article.

LITERATURE CITED

Bouchet, P. and R. Petit. 2002. New species of deep-water Cancellariidae (Gastropoda) from the southwestern Pacific. The Nautilus

116: 95—104.

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Volume 116

2002

AUTHOR INDEX

BAU GIO sera sat oianissias aaate selscisionin anenotb nse cislsw nlosenenamniaseen 89

[BKONUC aut IPL A Aad so bennsooend sag be sod as soso Od eOU ee Sate Ena NS 32, 95

OTRO NO New oer eae emia reas senate snare seats wisroun toa uhosinn 67

(GEG ENE'SINE: Rit sere ee eee seeps eo manana tere bey’ dat nai bars ie 89

(CRAIN Tihs, Wasi os oi atia se ome ae Ae ee ee er il

ID EVIRTESHGE [oactrussthspiswane ocecuimeias aceaec ss douisnnseemelindacengaiins 71

iD IDATRIO):. 18s sosdanasnangacessads su ceben ape dence Uae aH ner CREA Aaa 13

TRUATTAIVAINIRG? Jel nea pan ay dana nna nea Gane daoHOBe Aan aa ee eae 62

IE OIRINUINIATION 1B Bis eg oeeesoeanse ne camen bade nee need ance Sanaa ae aan 59

(COMBS: S.URs pase sowcotngaseenssonsbonossnoeae nas uscocnueee aan aaess 79

EVAR ENCE Mn Gacy orci eceanceearbienninacsenciicindse aie 129

lnriuaininiag,’ (Gp obeosbancnuan cue sense cesene Un ceserae ne ance nc er enn ae ete 109

|ORINGOIN, INGE Sececostoqnessrebeehaacsasesaaneteencre ap apmeemnceees 132

[LIDANGS, | Jp 18 Boece Aneoddsonstbeeddberpretocdad score ipso race eaten tremens 69

TLIBONIARID, NAL JP aca aoeseccat cas sce meson os baa aoe Ronee aBOn Deena 89

TLii@uitay: Avs vy a seseiaeadie es see tet re age ee ae ov mo aa 50

IMLATRGISUATIE TB)S UAE Res car ae are saan ina onl Sealer ea ee Sa 66

INDINTE@ Neier Reese ince on eon Onna sosticts. ys hem enoor mateiae OO)

INGA CETTE V Bee rere erst re cen rN a Ec Sih opie, AM aN ta 13

INDIES ANS), Scan aoe non sosonberssninesudoncausustareesnneDeeonanaate 71

COKIN GH] Kara hn oot Ss OH a a AD OAT A aR ne TAUB GRE pe anameEonee obs 89

AGTORUN an Geer ee eer oer ceo aise lee 105

REN CHAS Z/ATD EB Hee aire apse saerrseraieveis dehvoclasanistek acien aeseeeren 105

JRASH TAD Bind iG Gucte anne sae AR ORG Sen ONT aACERE OORT OT AH GRADUATE 95, 129

TRUSTS ed oe vas er eee ne eatery ore ese Gana en a ae 89

RU Coan Uae Nes Hos, Ait hae dae OS Dann A URtan ea mannii a ane anrtemrea ss ayn 36

SCHONE SB be Peer beacon one eee CEE an REE ee Chee

STTEWARE REO Pn anle Senet ee eee OI CE TA LOTS 79

SND ER Gi Naka Av ona eadereet tae eters eae st cece nr eereiavastecine eos 56

ISOS, Jo. \Wonosodooosossonouaacnossneso0nnnssodadaenaosoanbovosooan 79

AVA SIGUA Riberaee oan as Jase SAA SBEE AO AGRO ORS On Na RES OnE EN Reema tr 50

MECAUIR Ue erence itr aaa Penn meaner earner 50

VVADETERS a Grails cerry Sate arecis MErnreT iinet aan cre nee 118

TAT WSN] Dl Gas neon nceH et oant SAO Oue EOS OBE UASAORG ER ORG TR AAES 109

NEW TAXA PROPOSED IN VOLUME 116 (2002)

GASTROPODA

Aiineontonade pinumn Bouchet and: betty 2002smews species) (Cancellaridac) manne ceases eee eee eee een ae 96

Coralliophila kaofitorum Vega, Vega and Luque, 2002, new species (Coralliophilidae) ...........000....ccceeeeceeeeeeeeeeeeeeeeneees 51

Fusius doupdadi Sanpete, A002, men gesoies (BESCORTANGENS)) « .40020020300000000000900000950009000008008AdeNqcuaddan9E0—ss0HGAnUDRADDDAINRAOG 56

Mimanaapnenacayre: bouche anduetites002.mewaspecies (Cancellamidae) -sereeeeeer eee eee ee se eee eee eee 97

Mirandaphera maestratii Bouchet and Petit, 2002, new species (Cancellariidae).................:ccccceeceeeeeneeeeeceeeeteeeeeseeeeeees 98

Menicammunscompouchetand Petite: 2002 snewaspecies) Cancellariidae) eae seen eee eee eceee eee seeeeeeeeeeeeee 98

Nipponaphera pardalis Bouchet and Petit, 2002, new species (Cancellariidae)...................cescceeeeeeecenseeneeeeeeeeeteeeeeseeees 102

Nipponaphera cyphoma Bouchet aud Petit) 2002) newrspecies (Cancellaritdae)s..-).212-e reson ee eene eee eee oss see nes eeeeeee ese 102

Nipponapnerazoniatasbouchewandsetity 2002smews species) (Cancellaridae) sp wereeeyereeeee ees eeeee eee eeeeeee cee eee 103

Socimamocronusbouchetsandebetites2002-enewaspeciess (Cancellanidae) serene eee cee eee eee eee eee eee 100

Sucimomspiendiduiaa ouchewanderetites 2002smewsspeciess\Cancellanidae) aes eee ee teen eee ee cee eee e eee 100

Trigonostoma mozambicense Petit and Harasewych, 2002, new species (Cenc n GIGS) 5 oanacongoosessoaoocosseanasoneaasaccadansoas 129

BIVALVIA

Waldosnapexalis Zelayavand Ituaxtes)20025mew-species (Galleomatidae) ss .--e-eeae see e eee eee eee eee cee 115

Alan G. Beu

Philippe Bouchet

Hank W. Chaney

Roberto Cipriani

Eugene V. Coan

Robert H. Cowie

Kevin Cummings

Charles D’Asaro

H. Lee Fairbanks

Matthias Glaubrecht

REVIEWERS FOR VOLUME 116

Terrence M. Gosliner

Roland Hadorn

M. G. Harasewych

Sadao Kosuge

Gijs C. Kronenberg

Kevin Lamprell

William G. Lyons

Bruce A. Marshall

Paula M. Mikkelsen

Patricia Miloslavich

Brian Morton

Timothy Pearce

Richard E. Petit

Paul H. Scott

John Slapeinsky

Ellen E. Strong

Kazushige Tanabe

Angel Valdés

Anders Warén

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