European Journal of Taxonomy 154: 1-7
http://dx.doi.org/10.5852/eit.2015.154
www. europeani ournaloftaxonomv. eu
2015 • Reuscher M.G.
ISSN 2118-9773
This work is licensed under a Creative Commons Attribution 3,0 License.
Research article
um:lsid:zoobank.org:pub:F9A2F05E-0F3A-4459-BB5F-FC8563DD683C
Amage imajimai sp. nov., a new species of Ampharetidae
(Annelida: Polychaeta) from Japanese waters
Michael G. REUSCHER
Harte Research Institute for Gulf of Mexico Studies, Texas A&M University - Corpus Christi, 6300
Ocean Drive, Unit 5869, Corpus Christi, Texas 78412-5869, USA.
um:lsid:zoobank.org:author:CEE857C6-DB17-4C9B-BE81-D04AB815E909
Abstract. A new polychaete species of the family Ampharetidae, Amage imajimai sp. nov., is described
from deep waters of Sagami Bay, Japan. It is characterized by the possession of four pairs of branchiae,
twelve thoracic uncinigers, eleven abdominal uncinigers, and the lack of thoracic notopodial cirri.
The new species is named in honor of the renowned Japanese polychaetologist Minoru Imajima. An
identification key for all Amage species from Japanese waters is provided.
Keywords. Ampharetidae, Amage , new species, Sagami Bay, Japan.
Reuscher M.G. 2015. Amage imajimai sp. nov., a new species of Ampharetidae (Annelida: Polychaeta) from
Japanese waters. European Journal of Taxonomy 154: 1-7. http://dx.doi.org/10.5852/eit.2015.154
Introduction
In a recent study on Ampharetidae from Japan many new species and new records were discovered
(Imajima et al. 2012, 2013; Reuscher et al. 2015a, 2015b). In the last publication of the series (Reuscher
et al. 2015b), a list of all 58 ampharetid species recorded from Japan was provided. Six of these species
known to occur in Japanese waters belong to the genus Amage Malmgren, 1866: A. cf. adspersa
(Grube, 1863), A. auricula Malmgren, 1866, A. delus (Chamberlin, 1919), A. ehlersi Reuscher, Fiege &
Imajima, 2015, A. longitorus Reuscher, Fiege & Imajima, 2015 and A. scutata Moore, 1923. During the
examination of material from the National Museum of Nature and Science in Tsukuba (Japan), I was
able to identify another new species of Amage, which is described here. The new species was collected
at a depth of about 1000 m in Sagami Bay off the southeastern Honshu coast.
Material and methods
The specimens examined in this study were collected in Sagami Bay during a research cruise in July
1966. They were fixed in 7% formaldehyde seawater solution and preserved in 70% ethanol.
Preserved specimens were examined with an Olympus SZX7 stereo microscope and compound
microscopes of the models Leica DMLB and Olympus CX41. Pencil drawings were made using a
camera lucida, attached to the Leica DMLB.
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European Journal of Taxonomy 154: 1-7 (2015)
The drawings were digitized with a Wacom Intuos drawing tablet and Adobe Illustrator, according to the
methods of Coleman (2003). Shadings were added in Adobe Photoshop. The “ID card” (Imajima et al.
2012) was prepared in Adobe Illustrator.
Abbreviations
cs = complete specimen
af = anterior fragment
Types and other specimens are deposited in the following institutions:
NSMT = National Museum of Nature and Science, Japan
SMF = Senckenberg Museum Frankfurt, Germany
Full details for the material deposited at Senckenberg can be found at http://sesam.senckenberg.de/ .
Results
Phylum Annelida Lamarck, 1809
Class Polychaeta Grube, 1850
Order Terebellomorpha Hatschek, 1893
Family Ampharetidae Malmgren, 1866
Subfamily Ampharetinae Malmgren, 1866
Genus Amage Malmgren, 1866
Amage Malmgren, 1866: 370.
Par amage Caullery, 1944: 94.
Egamella Fauchald, 1972: 295.
Mexamage Fauchald, 1972: 309.
Type species
Amage auricula Malmgren, 1866.
Diagnosis (emended)
Prostomium with middle lobe surrounded by inflated lobe, lacking glandular ridges. Buccal tentacles
smooth. Two to four pairs of cirriform branchiae. Segment II usually without chaetae, or exceptionally
with minute chaetae. Thorax with 9-14 uncinigers. Modified or intermediate segments absent. Abdomen
with rudimentary notopodia.
Remarks
The diagnosis was emended to accommodate the synonymy of the monotypic genus Egamella Fauchald,
1972 by Jirlcov (2011). Egamella has only two pairs of branchiae and nine thoracic uncinigers. This
synonymy needs to be confirmed by the examination of the type specimen of Egamella quadribranchiata
Fauchald, 1972.
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REUSCHER M.G., New Amage species from Japan
Amage imajimai sp. nov.
urn:lsid:zoobank.org:act:CCA76C94-C953-418D-AFC9-DDBBD7D99C6D
Fig. 1A-G
Diagnosis
Four pairs of branchiae. Twelve thoracic uncinigers. Notopodia without ventral cirri. Eleven abdominal
uncinigers.
Etymology
The species is dedicated to the distinguished Japanese polychaete taxonomist Minoru Imajima.
Specimens examined
Holotype
JAPAN: SMF 24087, Sagami Bay, 35°00.9’ N, 139°35.7’ E - 35°00.7’ N, 139 o 36.0’ E, 990-1060 m,
KT-66-12, St. 7, Jul. 1966 (1 cs).
Paratypes
JAPAN: SMF 24086, same locality as holotype (3 cs); NSMT-Pol. P-600, same locality as holotype
(3 cs, 1 af).
Description
Length of holotype 3.2 mm, width 0.4 mm Prostomium with middle lobe bearing anterolateral frontal
horns, delimited by incision from inflated surrounding lobe (Fig. 1A); prostomium without glandular
ridges or eyes. Single tip of smooth buccal tentacle visible in buccal cavity. Four pairs of branchiae
in L-shaped arrangement in segments II-IV (Fig. IB), separated by wide median gap; all branchiae
detached from specimen, cirriform, without conspicuous ciliation or annulations; innermost branchiae
of anterior transverse row (1) originating from segment II, outermost branchiae of anterior transverse
row (2) originating from segment III, median branchiae of longitudinal row (3) originating from
segment IV, posterior branchiae of longitudinal row (4) originating from segment V (Fig. IB). Segment
II without chaetae. Notopodia with capillary chaetae from segment III, present in 15 chaetigers; first
three notopodia in close succession due to shortness of segments and slightly elevated above following
notopodia (Fig. 1C); first notopodia small, increasing in size from first to third pair; notopodial cirri
absent. Neuropodial tori with uncini from segment VI, present in 12 thoracic uncinigers; tori without
cirri. Continuous ventral shields conspicuous from anterior thorax to thoracic unciniger 9. Modified
notopodia or segments absent. Intermediate uncinigers absent. Eleven abdominal uncinigers with
small tuberculate rudimentary notopodia. Pinnules with minute tuberculate dorsal cirrus. Rudimentary
notopodia and pinnules connected by glandular fold. Pygidium with one pair of digitiform, ventrolateral
anal cirri. Left anal cirrus broken off. Thoracic uncini with 7 teeth in 2 staggered row over basal prow
and rostral tooth (Fig. 1D-E). Abdominal uncini with numerous teeth in several rows over basal prow
and rostral tooth. Tube parchment like with needle like spicules embedded.
Remarks
In four of the paratypes the buccal tentacles are better visible and clearly smooth. The tuberculate dorsal
cirri of the abdominal pinnules are much better developed in the larger paratype specimens (Fig. IF).
The anal cirri are longer and cirriform in the larger paratypes (Fig. 1G). However, they also seem to
break off easily as three of the six complete paratypes lack both anal cirri.
The two other Amage species with twelve thoracic uncinigers are A. benhami Reuscher, Fiege & Wehe,
2009 from the northeast Pacific and the Ross Sea and A. longitorus Reuscher, Fiege & Imajima, 2015
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European Journal of Taxonomy 154: 1-7 (2015)
Fig. 1 . Amage imajimai sp. nov. A. Anterior end of holotype, dorsal view. B. “ID card”. C. Anterior
end of holotype, lateral view. D. Thoracic uncinus, lateral view. E. Thoracic uncinus, frontal view.
F. Abdominal uncinigers, lateral view (from paratype SMF 24086). G. Posteriormost abdominal
uncinigers and pygidium, ventral view (from paratype SMF 24086).
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REUSCHER M.G., New Amage species from Japan
from Japan. The latter species differs from A. imajimai sp. nov. by the possession of only three pairs
of branchiae, the very long tori in the first two thoracic uncinigers and the larger number of abdominal
uncinigers (13). A. benhami differs from the new species by the presence of club shaped notopodial cirri
and the higher number of abdominal uncinigers (15-16).
Among the other Japanese Amage species A. auricula , A. delus , A. ehlersi and A. scutata have 11
thoracic uncinigers, A. cf. adspersa has 14 thoracic uncinigers. A. cf. adspersa, A. auricula and A.
delus differ from A. imajimai sp. nov. by the presence of notopodial cirri. A. scutata is unusual for the
presence of rudimentary notopodia in the anterior segments. A. imajimai sp. nov. has a higher count of
abdominal uncinigers (11) than A. auricula (8) and A. ehlersi (10) and a lower count than A. delus (12)
and A. longitorus (13).
Distribution
Sagami Bay on the Southeastern Pacific coast of Honshu, in 990-1060 m.
Identification key for Amage species from Japanese waters
1. 11 or 12 thoracic uncinigers.2
- 14 thoracic uncinigers. Amage cf. adspersa (Grube, 1863)
2.11 thoracic uncinigers.3
- 12 thoracic uncinigers.6
3. Anterior notopodia with notochaetae.4
- Anterior notopodia lacking notochaetae . Amage scutata Moore, 1923
4. Thoracic notopodia with ventral cirri.5
- Thoracic notopodia lacking ventral cirri. Amage ehlersi Reuscher, Fiege & Imajima, 2015
5. 8 abdominal uncinigers. Amage auricula Malmgren, 1866
- 12 abdominal uncinigers. Amage delus (Chamberlin, 1919)
6. 3 pairs of branchiae; anterior neuropodia conspicuously elongated; 13 abdominal uncinigers
. Amage longitorus Reuscher, Fiege & Imaj ima, 2 015
- 4 pairs of branchiae; anterior neuropodia not conspicuously elongated; 11 abdominal uncinigers
. Amage imajimai sp. nov.
Discussion
The variety of habitat types and complex interactions of different environmental gradients in the oceans
surrounding the Japanese islands attract a variety of species with different physiological and ecological
adaptations and thus form the basis of a diverse polychaete fauna. Japan has a wide variety of habitats
that are colonized by polychaetes, including bays, deep-sea trenches, hydrothermal vents, and cold
seeps, among others (e.g., Juniper & Sibuet 1987; Horilcoshi et al. 1990). The northern part of Japan
receives cold water from the Oyashio Current, whereas southern Japan is under the influence of the
warm Kuroshio Current (Imajima et al. 2012). Therefore, Japan’s polychaete fauna includes Arctic and
sub-Arctic species as well as tropical and subtropical species. In the recent series on Ampharetidae from
Japan (Imajima et al. 2012, 2013; Reuscher et al. 2015a, 2015b), 60% of the examined species were
new to science and the number of species known from Japan more than doubled. This shows that the
current knowledge of species diversity of ampharetid polychaetes from Japan is far from exhaustive and
more sampling effort is needed to complete the picture. Amage imajimai sp. nov. is the 59 th species of
the family Ampharetidae and the seventh species of the genus Amage recorded from Japan.
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European Journal of Taxonomy 154: 1-7 (2015)
Of the other Amage species from Japan, A. delus and A. scutata are known only from northern Honshu,
A. cf. adspersa and A. imajimai sp. nov. have only been recorded from Sagami Bay, whereas A. auricula ,
A. ehlersi and A. longitorus have a wider distribution within Japanese waters.
Within Ampharetidae Amage is probably the most heterogeneous genus as it contains species with
two (if the genus Egamella is considered a junior synonym), three and four pairs of branchiae, with
nine ( Egamella ), eleven, twelve, and fourteen thoracic uncinigers, with and without notopodial cirri.
A revision is needed to determine if Amage can be upheld as a single genus, or if it should be split into
multiple genera.
Acknowledgements
Min oru Imajima (NSMT) is thanked for the loan of the specimens. I am grateful to Richard D. Kalke
and Fabio Moretzsohn (Harte Research Institute, Texas A&M University-Corpus Christi) for their
permissions to use their camera lucida. Paul A. Montagna (Harte Research Institute, Texas A&M
University-Corpus Christi) is thanked for his financial support through the Texas Research Development
Post-Doctoral Support Grant.
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Manuscript received. 14 August 2015
Manuscript accepted. 8 October 2015
Published on: 19 November 2015
Topic editor. Rudy Jocque
Desk editor. Kristiaan Hoe demakers
Printed versions of all papers are also deposited in the libraries of the institutes that are members of the
EJT consortium: Museum national d’Histoire naturelle, Paris, France; Botanic Garden Meise, Belgium;
Royal Museum for Central Africa, Tervuren, Belgium; Natural History Museum, London, United
Kingdom; Royal Belgian Institute of Natural Sciences, Brussels, Belgium; Natural History Museum of
Denmark, Copenhagen, Denmark.
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