Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species

Paradialychone katsuuraensis new species Japanese name: Moba-Keyarimushi Figures 6–7 Material examined. Type material. HOLOTYPE — CBM –ZW– 557, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. PARATYPES —CBM-...

Full description

Bibliographic Details
Main Authors: Nishi, Eijiroh, Tanaka, Katsuhiko, Tovar-Hernández, María Ana, Giangrande, Adriana
Format: Text
Language:unknown
Published: Zenodo 2009
Subjects:
Online Access:https://dx.doi.org/10.5281/zenodo.5234000
https://zenodo.org/record/5234000
id ftdatacite:10.5281/zenodo.5234000
record_format openpolar
institution Open Polar
collection DataCite Metadata Store (German National Library of Science and Technology)
op_collection_id ftdatacite
language unknown
topic Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Sabellida
Sabellidae
Paradialychone
Paradialychone katsuuraensis
spellingShingle Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Sabellida
Sabellidae
Paradialychone
Paradialychone katsuuraensis
Nishi, Eijiroh
Tanaka, Katsuhiko
Tovar-Hernández, María Ana
Giangrande, Adriana
Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
topic_facet Biodiversity
Taxonomy
Animalia
Annelida
Polychaeta
Sabellida
Sabellidae
Paradialychone
Paradialychone katsuuraensis
description Paradialychone katsuuraensis new species Japanese name: Moba-Keyarimushi Figures 6–7 Material examined. Type material. HOLOTYPE — CBM –ZW– 557, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. PARATYPES —CBM-ZW- 552, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW 554, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW- 555, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW- 561, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, Coll. E. Nishi by hand. ECOSUR 0 0 91, same collection data as holotype. Description. Body brown, glandular girdle white and branchial crown pale in live specimens (Figure 6 A–B photo of live worms). Body cylindrical, posterior abdomen inflated in some specimens (Figure 6 B). Adult holotype 40 mm long excluding radioles, 50–80 mm in paratypes, width 0.5 mm in posterior thorax in holotype, 1.6 to 2.0 mm in paratypes. Branchial crown length 6.0 mm in holotype, 7.0 mm in largest paratypes. Insertion of branchial lobes not exposed beyond collar (Figures 6 C–D, 7 B–C). Base of branchial crown shorter than collar segment. Branchial crown length 6.0 mm in holotype, 5.0–7.0 mm in paratypes. Ten pairs of radioles in holotype, 10–12 in paratypes, connected for almost entire length by palmate membrane (Figure 7 D–E). Radioles with longest pinnules three quarters of their length. Radiolar tips filiform (Figure 7 E–F). Lateral flanges narrow along the outer edges of radioles. Dorsal lips with radiolar appendages (Figure 7 G). A variable number of dorsal pinnular appendages, from 1 to six, 1 in holotype (Figure 7 G), with different lengths. Paired ventral lips same lengths as dorsal lips, pointed (Figure 7 G). Ventral radiolar appendages absent. Ventral peristomial lobe projection triangular with entire tip (Figure 7 C), not exposed beyond collar or slightly exposed beyond collar. Collar margin entire, ventral margin slightly higher than lateral and dorsal (Figure 7 B–C), reaching approximately to base of branchiae. Dorsal gap narrow. Dorsal pockets present. Collar slightly higher ventrally than dorsally in lateral view. Peristomial ring collar 1.5 times longer than chaetiger 2 in lateral view. Ventral shield of collar undifferentiated (pentagonal-shaped using methyl green, Figure 6 C). Chaetiger 2 glandular girdle present, slightly wider dorsally than ventrally (Figures 6 C–D, 7 A–C, I–J). Ventral shields not discernible (Figures 6 C, 7 A). First thoracic chaetiger with single row of long, narrowly hooded chaetae. Following thoracic segments with three kinds of notochaetae: superior group of long narrowly hooded chaetae, inferior group with short limbate chaetae and paleate chaetae with a minute mucros or completely rounded (Figures 6 E–F, 7 N) and slender pointed bayonet chaetae (Figure 7 K–L). Thoracic notopodia with 23 – 35 long-handled acicular uncini in each fascicle, with five rows of unequal in size teeth in lateral and frontal views (Figures 6 G, 7 M), covering proximal half of main fang. Abdomen with 40 chaetigers in holotype, 40–45 in paratypes. Anterior abdominal notopodial tori with 14–40 uncini, each with quadrate base (Figure 7 P–Q), and first tooth over main fang larger than following three rows of teeth (Figures 6 H, 7 P). Shape of uncini nearly constant within each torus, but main fang progressively smaller in posterior chaetigers. In posterior abdomen, uncini rasp-shaped (Figures 6 I, 7 Q); teeth equal size, covering three quarters of main fang length. Abdominal neuropodia with 13–14 narrowly hooded chaetae in two rows per fascicle. Posterior abdominal margin triangular, slightly longer than wide, without cirrus. Adult holotype (female). Sexes separate with gametes occurring laterally between dorsal and ventral longitudinal muscle bundles in posterior thoracic and abdominal chaetigers. Eggs with asynchronous development, up to 0.1 mm in diameter. Glandular pattern: Methyl green stain dorsally and ventrally (Figure 6 C–D) on most of the body including pygidium. Staining is absent in radioles, anterior margin of collar, glandular girdle on chaetiger 2, intersegmental furrow, fecal groove, around parapodia, and narrow band of cells encircling each segment at level of chaetae. Distribution: Paradialychone katsuuraensis is commonly found in shallow waters in Thalassia seagrass beds at Yoshio, Katsuura, Boso Peninsula (Figure 6 A). The species occurs in sandy to muddy substrates in depths of 0.5 to 5 m, in abundance occasionally exceeding 50 individuals/m 2. Remarks: In Paradialychone only three species have a glandular girdle on chaetiger 2 whose width is not homogeneous: in P. gambiae and P. paracincta (Hartmann-Schröder 1962) the girdle is wider laterally while in P. katsuuraensis wider dorsally. Also, P. g a m b i a e has a girdle on chaetiger 9 (absent in P. katsuuraensis n. sp. and P. paracincta ). Paradialychone katsuuraensis , P . eiffelturris and P. paramollis have paleate chaetae with minute mucros. In P. katsuuraensis , the girdle on chaetiger 2 is broad dorsally, and the ventral shield of collar is undifferentiated and pentagonal-shaped when is stained with methyl green (horseshoe-shaped in P. paramollis and Eiffel Tower-shaped in P. eiffelturris ). Paradialychone katsuuraensis is distributed in Japan while P. paramollis and P. eiffelturris are species with wide distribution in the Pacific coast of the United States. The new species is similar to Paradialychone ecaudata (= C. teres sensu Okuda 1934, 1946; Imajima and Hartman 1964); but the two are distinguished by following characters. In P . katsuuraensis the anterior peristomial ring lobe is triangular, not exposed beyond collar segment (Figures 7 B–C), and in P. ecaudata it is digitiform, and distinctly exposed beyond collar (Banse 1972: 475, Fig. 6 e; Tovar-Hernández 2007 a: 526, Fig 4 G). Paleate chaetae have long pointed tips in P. ecaudata but in P. katsuuraensis only minute tips or none at all (Figures 8 N, 9 E–F). Paradialyhone katsuuraensis and C. ecaudata are primarily differentiated in the presence of a glandular girdle on chaetiger 2 broad dorsally; the latter with a uniformly narrow ring. Paradialychone katsuuraensis is unique among congeners distributed in Japan by having a pentagonalshaped ventral shield on the collar, glandular girdle on chaetiger 2 broad dorsally, and paleate chaetae with minute mucros. For comparison, P. c i n c t a and P. katsuuraensis have a horseshoe-shaped ventral collar shield; P. c i n c t a have paleate chaetae with short mucros and P . edomae long mucros; P. c i n c t a and P. edomae have a narrow glandular girdle on chaetiger 2. Paradialychone katsuuraensis shares the same distribution with other species belonging to the related genera in Japan: Chone duneri , P. filicaudata (Southern, 1914), C. teres (Okuda 1934: 236, 1946: 171; Imajima and Hartman 1964: 365; Imajima 1961, 1963, see Banse 1972) and P . cincta Etymology: The specific epithet is named after type locality, Katsuura City, Boso Peninsula. The Japanese name Moba means seagrass bed, which the new specie commonly occurred (Figure 6 A), while· keyarimushi means sabellid polychaetes. : Published as part of Nishi, Eijiroh, Tanaka, Katsuhiko, Tovar-Hernández, María Ana & Giangrande, Adriana, 2009, Dialychone, Jasmineira and Paradialychone (Annelida: Polychaeta: Sabellidae) from Japan and adjacent waters, including four new species descriptions, pp. 1-24 in Zootaxa 2167 on pages 11-14, DOI: 10.5281/zenodo.189112 : {"references": ["Hartmann-Schroder, G. (1962) Zweiter Beitrag zur Polychaetenfauna von Peru. Kieler Meeresforschungen, 18, 109 - 147.", "Okuda, S. (1934) Some tubicolous annelids from Hokkaido. Journal of the Faculty of Science, Hokkaido University, Ser. VI, 3, 233 - 246.", "Okuda, S. (1946) Studies on the development of Annelida Polychaeta. I. Journal of the Faculty of Science, Hokkaido University, Ser. VI, 9, 115 - 219.", "Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan. Part II. Allan Hancock Foundation, Publication, Occasional Papers, 26, 239 - 452.", "Banse, K. (1972) Redescription of some species of Chone Kroyer and Euchone Malmgren, and three new species (Sabellidae, Polychaeta). Fishery Bulletin, Fish and Wildlife Service, USA Department of Interior, 70, 459 - 495.", "Tovar-Hernandez, M. A. (2007 a) Revision of Chone Kroyer, 1856 (Polychaeta: Sabellidae) from North America and descriptions of four new species. Journal of Natural History, 41, 511 - 566.", "Southern, R. (1914) Clare Island Survey: Archiannelida and Polychaeta. Proceedings of the Royal Irish Academy, 31, 1 - 160.", "Imajima, M. (1961) Polychaetous annelids collected off the west coast of Kamchatka. I. Notes on species found in the collection of 1957 - 58. Publications of the Seto Marine Biological Laboratory, 9, 81 - 102.", "Imajima, M. (1963) Polychaetous annelids collected off the west coast of Kamchatka. II. Notes on species found in the collection of 1959. Publications of the Seto Marine Biological Laboratory, 11, 345 - 372."]}
format Text
author Nishi, Eijiroh
Tanaka, Katsuhiko
Tovar-Hernández, María Ana
Giangrande, Adriana
author_facet Nishi, Eijiroh
Tanaka, Katsuhiko
Tovar-Hernández, María Ana
Giangrande, Adriana
author_sort Nishi, Eijiroh
title Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
title_short Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
title_full Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
title_fullStr Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
title_full_unstemmed Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species
title_sort paradialychone katsuuraensis nishi, tanaka, tovar-hernández & giangrande, 2009, new species
publisher Zenodo
publishDate 2009
url https://dx.doi.org/10.5281/zenodo.5234000
https://zenodo.org/record/5234000
long_lat ENVELOPE(167.217,167.217,-77.483,-77.483)
ENVELOPE(-66.117,-66.117,-65.750,-65.750)
ENVELOPE(-62.167,-62.167,-74.500,-74.500)
ENVELOPE(-62.783,-62.783,-64.667,-64.667)
geographic Pacific
Fang
Malmgren
Hernandez
Adriana
geographic_facet Pacific
Fang
Malmgren
Hernandez
Adriana
genre Kamchatka
genre_facet Kamchatka
op_relation http://publication.plazi.org/id/FF8EB15AFFF81921FFBD556EFFBEFF8F
https://zenodo.org/communities/biosyslit
https://dx.doi.org/10.5281/zenodo.189112
http://publication.plazi.org/id/FF8EB15AFFF81921FFBD556EFFBEFF8F
https://dx.doi.org/10.5281/zenodo.189118
https://dx.doi.org/10.5281/zenodo.189119
https://dx.doi.org/10.5281/zenodo.189116
https://dx.doi.org/10.5281/zenodo.189120
https://dx.doi.org/10.5281/zenodo.5234001
https://zenodo.org/communities/biosyslit
op_rights Open Access
info:eu-repo/semantics/openAccess
op_doi https://doi.org/10.5281/zenodo.5234000
https://doi.org/10.5281/zenodo.189112
https://doi.org/10.5281/zenodo.189118
https://doi.org/10.5281/zenodo.189119
https://doi.org/10.5281/zenodo.189116
https://doi.org/10.5281/zenodo.189120
https://doi.or
_version_ 1766051878614859776
spelling ftdatacite:10.5281/zenodo.5234000 2023-05-15T16:59:34+02:00 Paradialychone katsuuraensis Nishi, Tanaka, Tovar-Hernández & Giangrande, 2009, new species Nishi, Eijiroh Tanaka, Katsuhiko Tovar-Hernández, María Ana Giangrande, Adriana 2009 https://dx.doi.org/10.5281/zenodo.5234000 https://zenodo.org/record/5234000 unknown Zenodo http://publication.plazi.org/id/FF8EB15AFFF81921FFBD556EFFBEFF8F https://zenodo.org/communities/biosyslit https://dx.doi.org/10.5281/zenodo.189112 http://publication.plazi.org/id/FF8EB15AFFF81921FFBD556EFFBEFF8F https://dx.doi.org/10.5281/zenodo.189118 https://dx.doi.org/10.5281/zenodo.189119 https://dx.doi.org/10.5281/zenodo.189116 https://dx.doi.org/10.5281/zenodo.189120 https://dx.doi.org/10.5281/zenodo.5234001 https://zenodo.org/communities/biosyslit Open Access info:eu-repo/semantics/openAccess Biodiversity Taxonomy Animalia Annelida Polychaeta Sabellida Sabellidae Paradialychone Paradialychone katsuuraensis Taxonomic treatment article-journal Text ScholarlyArticle 2009 ftdatacite https://doi.org/10.5281/zenodo.5234000 https://doi.org/10.5281/zenodo.189112 https://doi.org/10.5281/zenodo.189118 https://doi.org/10.5281/zenodo.189119 https://doi.org/10.5281/zenodo.189116 https://doi.org/10.5281/zenodo.189120 https://doi.or 2022-02-08T13:42:09Z Paradialychone katsuuraensis new species Japanese name: Moba-Keyarimushi Figures 6–7 Material examined. Type material. HOLOTYPE — CBM –ZW– 557, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. PARATYPES —CBM-ZW- 552, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW 554, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW- 555, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, coll. E. Nishi by hand. CBM-ZW- 561, Yoshio, Katsuura, Boso Peninsula, subtidal sandy mud bottom, 1–5 m, among Thalassia marina thalli, 15 October, 1998, Coll. E. Nishi by hand. ECOSUR 0 0 91, same collection data as holotype. Description. Body brown, glandular girdle white and branchial crown pale in live specimens (Figure 6 A–B photo of live worms). Body cylindrical, posterior abdomen inflated in some specimens (Figure 6 B). Adult holotype 40 mm long excluding radioles, 50–80 mm in paratypes, width 0.5 mm in posterior thorax in holotype, 1.6 to 2.0 mm in paratypes. Branchial crown length 6.0 mm in holotype, 7.0 mm in largest paratypes. Insertion of branchial lobes not exposed beyond collar (Figures 6 C–D, 7 B–C). Base of branchial crown shorter than collar segment. Branchial crown length 6.0 mm in holotype, 5.0–7.0 mm in paratypes. Ten pairs of radioles in holotype, 10–12 in paratypes, connected for almost entire length by palmate membrane (Figure 7 D–E). Radioles with longest pinnules three quarters of their length. Radiolar tips filiform (Figure 7 E–F). Lateral flanges narrow along the outer edges of radioles. Dorsal lips with radiolar appendages (Figure 7 G). A variable number of dorsal pinnular appendages, from 1 to six, 1 in holotype (Figure 7 G), with different lengths. Paired ventral lips same lengths as dorsal lips, pointed (Figure 7 G). Ventral radiolar appendages absent. Ventral peristomial lobe projection triangular with entire tip (Figure 7 C), not exposed beyond collar or slightly exposed beyond collar. Collar margin entire, ventral margin slightly higher than lateral and dorsal (Figure 7 B–C), reaching approximately to base of branchiae. Dorsal gap narrow. Dorsal pockets present. Collar slightly higher ventrally than dorsally in lateral view. Peristomial ring collar 1.5 times longer than chaetiger 2 in lateral view. Ventral shield of collar undifferentiated (pentagonal-shaped using methyl green, Figure 6 C). Chaetiger 2 glandular girdle present, slightly wider dorsally than ventrally (Figures 6 C–D, 7 A–C, I–J). Ventral shields not discernible (Figures 6 C, 7 A). First thoracic chaetiger with single row of long, narrowly hooded chaetae. Following thoracic segments with three kinds of notochaetae: superior group of long narrowly hooded chaetae, inferior group with short limbate chaetae and paleate chaetae with a minute mucros or completely rounded (Figures 6 E–F, 7 N) and slender pointed bayonet chaetae (Figure 7 K–L). Thoracic notopodia with 23 – 35 long-handled acicular uncini in each fascicle, with five rows of unequal in size teeth in lateral and frontal views (Figures 6 G, 7 M), covering proximal half of main fang. Abdomen with 40 chaetigers in holotype, 40–45 in paratypes. Anterior abdominal notopodial tori with 14–40 uncini, each with quadrate base (Figure 7 P–Q), and first tooth over main fang larger than following three rows of teeth (Figures 6 H, 7 P). Shape of uncini nearly constant within each torus, but main fang progressively smaller in posterior chaetigers. In posterior abdomen, uncini rasp-shaped (Figures 6 I, 7 Q); teeth equal size, covering three quarters of main fang length. Abdominal neuropodia with 13–14 narrowly hooded chaetae in two rows per fascicle. Posterior abdominal margin triangular, slightly longer than wide, without cirrus. Adult holotype (female). Sexes separate with gametes occurring laterally between dorsal and ventral longitudinal muscle bundles in posterior thoracic and abdominal chaetigers. Eggs with asynchronous development, up to 0.1 mm in diameter. Glandular pattern: Methyl green stain dorsally and ventrally (Figure 6 C–D) on most of the body including pygidium. Staining is absent in radioles, anterior margin of collar, glandular girdle on chaetiger 2, intersegmental furrow, fecal groove, around parapodia, and narrow band of cells encircling each segment at level of chaetae. Distribution: Paradialychone katsuuraensis is commonly found in shallow waters in Thalassia seagrass beds at Yoshio, Katsuura, Boso Peninsula (Figure 6 A). The species occurs in sandy to muddy substrates in depths of 0.5 to 5 m, in abundance occasionally exceeding 50 individuals/m 2. Remarks: In Paradialychone only three species have a glandular girdle on chaetiger 2 whose width is not homogeneous: in P. gambiae and P. paracincta (Hartmann-Schröder 1962) the girdle is wider laterally while in P. katsuuraensis wider dorsally. Also, P. g a m b i a e has a girdle on chaetiger 9 (absent in P. katsuuraensis n. sp. and P. paracincta ). Paradialychone katsuuraensis , P . eiffelturris and P. paramollis have paleate chaetae with minute mucros. In P. katsuuraensis , the girdle on chaetiger 2 is broad dorsally, and the ventral shield of collar is undifferentiated and pentagonal-shaped when is stained with methyl green (horseshoe-shaped in P. paramollis and Eiffel Tower-shaped in P. eiffelturris ). Paradialychone katsuuraensis is distributed in Japan while P. paramollis and P. eiffelturris are species with wide distribution in the Pacific coast of the United States. The new species is similar to Paradialychone ecaudata (= C. teres sensu Okuda 1934, 1946; Imajima and Hartman 1964); but the two are distinguished by following characters. In P . katsuuraensis the anterior peristomial ring lobe is triangular, not exposed beyond collar segment (Figures 7 B–C), and in P. ecaudata it is digitiform, and distinctly exposed beyond collar (Banse 1972: 475, Fig. 6 e; Tovar-Hernández 2007 a: 526, Fig 4 G). Paleate chaetae have long pointed tips in P. ecaudata but in P. katsuuraensis only minute tips or none at all (Figures 8 N, 9 E–F). Paradialyhone katsuuraensis and C. ecaudata are primarily differentiated in the presence of a glandular girdle on chaetiger 2 broad dorsally; the latter with a uniformly narrow ring. Paradialychone katsuuraensis is unique among congeners distributed in Japan by having a pentagonalshaped ventral shield on the collar, glandular girdle on chaetiger 2 broad dorsally, and paleate chaetae with minute mucros. For comparison, P. c i n c t a and P. katsuuraensis have a horseshoe-shaped ventral collar shield; P. c i n c t a have paleate chaetae with short mucros and P . edomae long mucros; P. c i n c t a and P. edomae have a narrow glandular girdle on chaetiger 2. Paradialychone katsuuraensis shares the same distribution with other species belonging to the related genera in Japan: Chone duneri , P. filicaudata (Southern, 1914), C. teres (Okuda 1934: 236, 1946: 171; Imajima and Hartman 1964: 365; Imajima 1961, 1963, see Banse 1972) and P . cincta Etymology: The specific epithet is named after type locality, Katsuura City, Boso Peninsula. The Japanese name Moba means seagrass bed, which the new specie commonly occurred (Figure 6 A), while· keyarimushi means sabellid polychaetes. : Published as part of Nishi, Eijiroh, Tanaka, Katsuhiko, Tovar-Hernández, María Ana & Giangrande, Adriana, 2009, Dialychone, Jasmineira and Paradialychone (Annelida: Polychaeta: Sabellidae) from Japan and adjacent waters, including four new species descriptions, pp. 1-24 in Zootaxa 2167 on pages 11-14, DOI: 10.5281/zenodo.189112 : {"references": ["Hartmann-Schroder, G. (1962) Zweiter Beitrag zur Polychaetenfauna von Peru. Kieler Meeresforschungen, 18, 109 - 147.", "Okuda, S. (1934) Some tubicolous annelids from Hokkaido. Journal of the Faculty of Science, Hokkaido University, Ser. VI, 3, 233 - 246.", "Okuda, S. (1946) Studies on the development of Annelida Polychaeta. I. Journal of the Faculty of Science, Hokkaido University, Ser. VI, 9, 115 - 219.", "Imajima, M. & Hartman, O. (1964) The polychaetous annelids of Japan. Part II. Allan Hancock Foundation, Publication, Occasional Papers, 26, 239 - 452.", "Banse, K. (1972) Redescription of some species of Chone Kroyer and Euchone Malmgren, and three new species (Sabellidae, Polychaeta). Fishery Bulletin, Fish and Wildlife Service, USA Department of Interior, 70, 459 - 495.", "Tovar-Hernandez, M. A. (2007 a) Revision of Chone Kroyer, 1856 (Polychaeta: Sabellidae) from North America and descriptions of four new species. Journal of Natural History, 41, 511 - 566.", "Southern, R. (1914) Clare Island Survey: Archiannelida and Polychaeta. Proceedings of the Royal Irish Academy, 31, 1 - 160.", "Imajima, M. (1961) Polychaetous annelids collected off the west coast of Kamchatka. I. Notes on species found in the collection of 1957 - 58. Publications of the Seto Marine Biological Laboratory, 9, 81 - 102.", "Imajima, M. (1963) Polychaetous annelids collected off the west coast of Kamchatka. II. Notes on species found in the collection of 1959. Publications of the Seto Marine Biological Laboratory, 11, 345 - 372."]} Text Kamchatka DataCite Metadata Store (German National Library of Science and Technology) Pacific Fang ENVELOPE(167.217,167.217,-77.483,-77.483) Malmgren ENVELOPE(-66.117,-66.117,-65.750,-65.750) Hernandez ENVELOPE(-62.167,-62.167,-74.500,-74.500) Adriana ENVELOPE(-62.783,-62.783,-64.667,-64.667)