A new species of the genus Sabellaria Lamarck, 1812 (Annelida: Polychaeta: Sabellariidae), is described from shallow water off Tottori, the Sea of Japan. Sabellaria tottoriensis n. sp., is gregarious with tubes constructed of sand and shell debris. The new species is distinguished by the character combination of 1 or 2 pairs of nuchal spines, two forms (long and short) of opercular paleae in the middle row, with the slender blades of long ones recurved outward. Detailed morphological features of the species are described and compared with other Japanese and worldwide congeners.
Species of the genus Sabellaria (Annelida: Polychaeta: Sabellariidae) are distributed worldwide from shallow waters to great depths. Some Sabellaria species are known as reef-builders making them the subject of ecological and paleontological interest as well as of systematic and biogeo-graphical importance (e.g., Caline et al., 1992; Pandolfi et al., 1998; Wood, 1999).
Kirtley's (1994) monograph deals with the systematics of the family Sabellariidae, referring to all valid species and available names at that time, comprising 33 presently known species of Sabellaria. From Japanese waters, 2 species of the genus have been reported: Sabellaria ishikawai Okuda, 1938 and S. cf. chandraae de Silva, 1961 (Nishi and Kato, 2002). We here describe a new species of the genus Sabellaria, as the third species of the genus from Japan.
This species abruptly appeared in 2001 as an explosive population together with a serpulid polychaete, Hydroides ezoensis Okuda, 1934, both densely attaching on the shell of living turbo Turbo torquatus Gmelin, 1791 (Fig. 1).
MATERIALS AND METHODS
The worms were collected off the Tottori Prefectural Fisheries Research Center, Ishiwaki, Tomari, Tohaku, Tottori Prefecture, at 2–6 m depth.
Worms and tubes were fixed in 10% seawater formalin together with the Turbo shell, on which the tubes of the worms were tightly attached. Some tubes were broken and about 25 worms removed. Another 10 or more specimens were preserved inside their tubes in order to conserve tube morphology. All specimens were preserved in 70% Ethanol.
The external morphology of the specimens was examined using a stereomicroscope. For detailed observation of the fine structure, chaetae and paleae were dissected, mounted on glass slides, and examined using a phase-contrast microscope.
The specimens were compared to the following specimens of Japanese Sabellaria, deposited in the Coastal Branch of Natural History Museum and Institute, Chiba (CMNH):
Sabellaria ishikawai Okuda, 1938. CMNH-ZW00904, 00905, 00997; Shimoda, Shizuoka Prefecture, 40m deep, 20 October, 1999, by dredge, coll. by R. Ueshima.
Sabellaria cf. chandraae de Silva, 1961. CMNH-ZW01201; Ubara-Island, Katsuura, Chiba Prefecture, 10–15 m deep, 14 August, 1997, coll. by CMNH.
The following abbreviations are used in the text:
Australian Museum, Sydney, Australia
Natural History Museum and Institute, Chiba, Japan
Coastal Branch of the Natural History Museum and Institute, Chiba, Japan
Natural History Museum of Los Angeles County, Allan Hancock Foundation Polychaete Collection, U.S.A.
Muséum national d'Histoire naturelle, Paris, France
Museo Nacional de Ciencias Naturales, Madrid, Spain
The Natural History Museum, London, U. K.
Museum & Art Gallery of the Northern Territory, Australia
Royal British Columbia Museum, Canada
South Australian Museum, Sydney, Australia SMBL Seto Marine Biological Laboratory, Kyoto University, Wakayama, Japan
Senckenberg Museum, Frankfurt, Germany
Shimoda Marine Research Center, Tsukuba University, Shimoda, Shizuoka, Japan
The Smithsonian Institution, National Museum of Natural History, Washington D. C., U. S. A.
Zoological Institute, Hokkaido University, Hokkaido, Japan
Zoological Museum of Hamburg, Germany
Family Sabellariidae Johnston, 1865
Genus Sabellaria Lamarck, 1812
Sabellaria tottoriensis n. sp.
HOLOTYPE'CMNH-ZW01515, on shell of living Turbo torquatus, with tube constructed of sand and shell debris, collected off Tottori Prefectural Fisheries Research Center, Ishiwaki, Tomari, Tohaku, Tottori Prefecture, Japan, 2–6 m, 20 March 2002, by SCUBA-diving, coll. N. Matsuda. PARATYPES, 25 specimens (AM W29058; CBM-ZW-946; CMNH-ZW01507-01514; LACM-AHF POLY 2127; MNCN 16.01/9952; MNHN POLY TYPE 1436; NTM W18657; NHM 2003.815-816; RBCM 003-00142-001; SAM E3346, E3347; SMBL Type No. 415; SMF 12898∼12902; SMRC-POL-002; USNM 1017840; ZIHU -3065; ZMH P-24533), collection data same as for holotype.
Holotype immature specimen, lacking distal end of cauda, 6.0 mm long, 0.9 mm wide at widest part of opercular crown, 1.0 mm wide at parathoracic chaetigers. Paratypes 5.0–13.0 mm long, 0.8–1.2 mm wide at parathoracic chaetigers. Anterior end of opercular stalk completely divided into 2 bilaterally symmetrical lobes. Lobes narrowing anteriorly, sloping posteriorly toward dorsal midline (Fig. 2A, C). Opercular paleae in three concentric rows. Paleae bright yellow, with light pink or colorless bases (embedded in tissue). Outer row with 20-25 flattened, rectangular paleae on each side (Fig. 3B, G).
Outer paleae ca. 0.5 mm long and ca. 0.1 mm wide, curved slightly outward from longitudinal axis of shaft. Inner surface of blade with ca. 50 fine, closely-spaced thecal bands (Fig. 3G). Distal ends of outer paleae with single median plume and 3–4 pairs of distal lateral teeth with sharp tips (N=18, average=3.27, SD=0.46: paratype CMNHZW01508; Fig. 3B, G). Median plume extended, ca. 0.15 mm long, denticulate with 8–12 small lateral teeth on each side (N=18, average=10.8, SD=1.1: paratype CMNHZW01508), decreasing in size distally (Fig. 3G). Distal lateral teeth and lateral teeth of plume occasionally continuous and difficult to separate from each other resulting in a total number 11-17 for distal lateral and lateral teeth of plume (N=18, average=14.5, SD=1.40: paratype CMNH-ZW01508).
Middle paleae including two forms, i.e. long and short. Long form 4–6 pairs, with blade erect, tapering slowly to blunt tip, recurved outward towards outer margin of crown (Figs. 2A, B, C and 3C). Short form 5–6 pairs, geniculate, with thick, wide blade terminating distally in blunt tip (Fig. 3D). Inner surface of short form excavate in basal part (Fig. 3C, D). Blades of long and short form with thecal bands (Fig. 3D, F)
Inner paleae with 10–14 pairs, similar in shape to short form of middle paleae, but usually smaller in size with shorter blades (Fig. 3E, H). Surface of excavated blade with thecal bands (Fig. 3H). One or 2 dorsal nuchal spines arising from each side of dorsal midline (Fig. 2B), usually crossing each other. Blades semi-transparent, colorless, slender, straight, with blunt tips (Fig. 3A).
Anterior outer margin of opercular crown with 8–10 fleshy conical papillae in single row on each side (Fig. 2B, C). Ventral margin of buccal cavity with 10–15 longitudinal rows of feeding tentacles on each side (Fig. 2A). Building organ U-shaped, with conical cirri, forming upper lip on ventral side (Fig. 2A).
Inferior lobes of second chaetiger with fascicle of ca. 7 bipinnate, capillary chaetae and conical lateral cirrus (Fig. 2C). Superior lobes with achaetous conical cirri along lateral margin of opercular lobe, with dorsal conical branchiae (Fig. 2C).
Three parathoracic chaetigers with 8–10 stout, oar-shaped chaetae and spine-like companion chaetae in 2 or 3 rows on each of neuropodia and ca. 10 chaetae on each of notopodia.
Abdominal part with 17 chaetigers in holotype, 10–30 in paratypes, with bundles of 10–15 long simple capillaries and finely serrate neurochaetae, and elongate conical ventral cirri with an uncinigerous tori. Anterior-most 5–10 abdominal chaetigers with dorsal branchiae, diminishing in size posteriorly (Fig. 2A).
Cauda long and bent back on ventrum. Tube constructed of sand and shell debris, with inner side coated with thin membrane. Tube orifice 1.0 to 1.5 mm in diameter.
The species of Sabellaria are distinguished mainly by the features of their opercular crown, i.e. morphology and the number of paleae in each row and the presence or absence of nuchal spines (Kirtley, 1994). Sabellaria tottoriensis n. sp. differs from all other members of the genus in having both straight nuchal spines and long middle paleae with the tip curved toward periphery of crown.
Among the 33 species of Sabellaria described from all over the world, 9 species are known to have both nuchal spines and long middle paleae (Kirtley, 1994), however all of these species are different from S. tottoriensis n. sp. in having the long form of middle paleae with tips straight (e.g., S. floridensis Hartman, 1944).
When the morphology of middle paleae (long form) is considered, the present species resembles S. chandraae de Silva, 1961 from Sri Lanka (de Silva, 1961), S. cf. chandraae from Boso Peninsula, Japan (Nishi and Kato, 2002) and S. ranjhi (Hasan, 1960) from Pakistan, in having tip recurved toward the periphery of the crown. However, 1 or 2 nuchal spines are present on each side in S. tottoriensis n. sp., while absent in S. chandraae and S. ranjhi. Sabellaria tottoriensis n. sp. is also distinguished from other species with regard to the feature of outer paleae (Fig. 4). The present new species have a median plume and a row of distal lateral teeth on outer paleae (Fig. 4D), in contrast to the condition in S. javanica Augener, 1934, lacking distal lateral teeth and having only a hairy median plume (Fig. 4A). Sabellaria tottoriensis n. sp. is also clearly distinct from S. bellani Kirtley, 1994 having no median plume characteristically (Fig. 4B). All other 33 species of Sabellaria, including S. tottoriensis, have outer paleae possessing both distal lateral teeth and a median plume, however, are differentiated into several sorts in the detailed morphology. Sabellaria ranjhi and S. chandraae, bearing a close resemblance to S. tottoriensis in middle paleae, are also belonging to this group. Our present new species S. tottoriensis, however, has a median plume rather continuous with lateral teeth (Fig. 4D), while S. chandraae has pilose median plume (Fig. 4F) and S. ranjhi penicillate (Fig. 4E). These three species differ also with regard to the distal lateral teeth of the outer paleae, with 2 or 3 pairs of teeth in S. chandraae, 3 or 4 pairs in S. tottoriensis, and 5 pairs in S. ranjhi (Hasan, 1960; de Silva, 1961; Kirtley, 1994), although S. tottoriensis has a median plume indistinctly separated from lateral teeth (Fig. 3B, G).
Comparison of morphological characteristics among the Japanese species of Sabellaria.
From the China Sea, Yang and Sun (1985) reported S. alcocki Gravier, 1906, which resembles S. tottoriensis n. sp. in having outer paleae with 3 pairs of distal lateral teeth and a long denticulate median plume. However, S. tottoriensis n. sp. possesses 10–12 lateral teeth on the each side of median plume (Fig. 3B, G, and Fig. 4D), in contrast to the more numerous teeth (18–20) of S. alcocki (Fig. 4C). A nuchal spine is present in S. tottoriensis n. sp., while absent in S. alcocki.
Sabellaria tottoriensis n. sp. described here brings the number of species known for this genus to 34 worldwide and to 3 for Japanese waters. It represents the 11th species of Sabellariidae known from Japan. Nishi and Kirtley (1999) and Nishi and Kato (2002) summarized and reviewed the Japanese Sabellariidae, and provided a key. This key is revised as follows:
A Key to the Japanese Sabellariid species
1a Four parathoracic segments2 (genus Lygdamis)
1b Three parathoracic segments3
2a Outer palea straight, with pointed tipL. japonicus Nishi and Kirtley, 1999
2b Outer paleae curved distally, with stout rounded tipsL. curvatus (Johanssen, 1922)
3a Paleae in two rows4 (genus Idanthyrsus)
3b Paleae in three rows7
4a Outer paleae stout and straight, with a small number (1–15) of lateral teethI. saxicavus (Baird, 1863)
4b Outer paleae stout or thin, bent at tip, with 25 or more lateral teeth5
5a Outer paleae with thin lateral teeth, surface of paleae shaft marked by straight transverse lines at intervals about equal to shaft radiusI. okudai Kirtley, 1994
5b Outer paleae with stout lateral teeth6
6a Inner paleae shafts marked by fairly straight transverse lines at intervals below 0.1 of shaft radiusI. okinawaensis Nishi and Kirtley, 1999
6b Transverse lines in inner paleae shafts indistinctI. boninensis Nishi and Kirtley, 1999
7a Opercular lobes fused to each other8 (genus Neosabellaria)
7b Opercular lobes separated9 (genus Sabellaria)
8a Middle paleae all of long formN. cementarium (Moore, 1906)
8b Middle paleae short and long formsN. uschakovi Kirtley, 1994
9a Middle paleae all of short, lacking long form; nuchal spines absent; median plume of outer paleae denticulateS. ishikawai Okuda, 1938
9b Middle paleae two forms; long form erect and recurved toward periphery of crown; nuchal spines absent; outer paleae with pilose median plumeS. cf. chandraae de Silva, 1961
9c Middle paleae two forms; long form erect and recurved toward periphery of crown; A New Species of Sabellaria from Japan nuchal spine 1or 2 pairs; median plume of outer paleae indistinctly separated from lateral teeth S. tottoriensis n. sp.
We firstly thank Mr. Narufumi Matsuda, Tottori Prefectural Fisheries Research Center, for providing the specimens. We also thank Dr. Dieter Fiege, Senckenberg Museum, and anonymous reviewers for valuable comments on the ms. This study is partly funded by Kanagawa Academy of Science and Technology (KAST) Research Fund for E. N.
- H. Augener 1934. Polychaeten aus den zoologischen Museen von Leiden und Amsterdam, part IV. Zool Mededel Rijksmusnatur hist leyden 17:67–160. Google Scholar
- W. Baird 1863. Descriptions of several new species of worms belonging to the Annelida Errantia or tubicola of Milne-Edwards. Proc Zool Soc London 24:106–110. Google Scholar
- B. C. Caline, Y. Gruet, C. Legendre, J. L. Rhun, A. l'Homer, R. Mathieu, and R. Zbinden . 1992. The sabellariid reefs in the Bay of Mont Saint-Miche, France. Ecology, geomorphology, sedimentology, and geologic implications. Florida Oceanographic Society, Contribution to Marine Science 1:1–256. Edited and translated from French by Kirtley DW. Google Scholar
- C. Gravier 1906. Un Sabellarien vivant sur un Brachiopode (Kingena alcocki) Joubin. Bull Mus Nat Hist Natr 12:540–543. Google Scholar
- O. Hartman 1944. Polychaetous annelids. Part 6. Paraonidae, Magelonidae, Longosomidae, Ctenodrilidae, and Sabellariidae. Allan Hancock Pac Exp 10:311–389. Google Scholar
- S. A. Hasan 1960. Some polychaetes from the Karachi Coast. Ann Magaz Nat Hist London 13:103–112. Google Scholar
- K. E. Johanssen 1922. On some new tubicolous annelids from Japan, the Bonin Islands and the Antarctic. Ark Zool 15:1–11. Google Scholar
- D. W. Kirtley 1994. A review and taxonomic revision of the family Sabellariidae Johnston, 1865 (Annelida: Polychaeta). 223. pp. Sabecon Press. Florida. Google Scholar
- J. P. Moore 1906. Additional species of Polychaeta from the North Pacific. Proc Acad Nat Sci Philadelphia 58:217–260. Google Scholar
- E. Nishi and T. Kato . 2002. The Sabellariidae from Japan (Annelida: Polychaeta). Taxa (Proc Jap Soc Syst Zool) 13:5–17. in Japanese. Google Scholar
- E. Nishi and D. W. Kirtley . 1999. Three new species of Sabellariidae (Polychaeta) from Japan. Nat Hist Res 5:93–105. Google Scholar
- S. Okuda 1938. The Sabellariidae of Japan. J Fac Sci Hokkaido Univ Ser 6 Zool 6:235–253. Google Scholar
- J. M. Pandolfi, D. R. Robertson, and D. W. Kirtley . 1998. Roles for worms in reef-building. Coral Reefs 17:120. Google Scholar
- P. H. D. H. de Silva 1961. Contribution to the knowledge of the polychaete fauna of Ceylon. Spolia Zeylandica Natl Mus Ceylon 29:164–194. Google Scholar
- R. Wood 1999. Reef Evolution. 414. pp. Oxford Univ Press. New York. Google Scholar
- D. Yang and R. P. Sun . 1985. Polychaetous annelids commonly seen from the Chinese waters. Agriculture Publisher. Beijing. in Chinese with English abstract. Google Scholar
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