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Nicomache ohtai, new species (Polychaeta: Maldinidae) collected from the Hatsushima cold-seep in Sagami Bay PDF

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Preview Nicomache ohtai, new species (Polychaeta: Maldinidae) collected from the Hatsushima cold-seep in Sagami Bay

PROC. BIOL. SOC. WASH. 104(1), 1991, pp. 159-165 NICOMACHE OHTAI, NEW SPECIES (POLYCHAETA: MALDANIDAE) COLLECTED FROM THE HATSUSHIMA COLD-SEEP IN SAGAMI BAY Tomoyuki Miura and Jun Hashimoto —A Abstract. newmaldanidpolychaetespecies,Nicomacheohtai, isdescribed from the Hatsushima cold-seep in Sagami Bay at a depth of 1 163 m. The new species is very close to N. venticola from the hydrothermal vents ofthe north- eastern Pacific, however it differs from the latter in having up to 19 rostrate uncini with 3-4 apical teeth in each neuropodium instead ofup to 10 uncini with 2-3 teeth. Studies on Japanese cold-seeps began as this study, a new species ofthe genus M- a French-Japanese cooperative project us- comache is described based on intact spec- ing the French deep-sea submersible Nau- imens ofsome mature males and females. tilein 1984 andwere followed by multidis- The types are deposited in the National ciplinary surveys using the Japanese Science Museum, Tokyo (NSMT), the Ja- submersible Shinkai 2000 (Laubier et al. panMarineScienceandTechnologyCenter 1986, Miura 1988a). The collections from (JAMSTEC), and the National Museum of these programs have provided some inter- Natural History, Smithsonian Institution esting materials for polychaete taxonomy. (USNM). To date, all of the polychaetes that have been described are directly associated with Genus Mcomac/z^ Malmgren, 1865 alargerhost species atthe seep sites (Miura 1988b;Miura&Laubier 1989, 1990).These Nicomache ohtai, new species Figs. 1-3 associations include Protomystides hatsu- shimaensisattached to the openings ofves- Materialexamined.—WesternNorth Pa- timentiferan tubes and species ofthe Nau- cific, cold-seep communities off Hatsushi- tiliniellidae living in the mantle cavities of ma,SagamiBay,Japan.DSRVShinkai2000 bivalve mollusks. Free-living polychaetes Dive 450, 21 Oct 1989, 35°00.0'N, havenotbeenreportedfromtheseJapanese 139°13.5'E, 1163 m, collector J. Hashi- cold-seeps. However the second author did moto, holotype (NSMT-Pol. H-326), 3 collect maldanid polychaetes within tubes paratypes (USNM 127962), 4 paratypes thatwere attachedto a dead shell ofCalyp- (JAMSTEC); Dive 451, 22 Oct 1989, same m togena soyoae at 1 163 offHatsushima. site, collectorK. Fujikura, 1 paratype(JAM- Early important studies on the family STEC); unmanned submersible D3K, Dive MaldanidaeweremadebyArwidsson(1907, at Okinoyama Seep, Sagami Bay, 19 May 1911a, 1911b). Imajima & Shiraki (1982) 1989, 34°58.2'N, 139°31.4'E, 1116 m, 2 reviewedallJapanesemaldanidpolychaetes paratypes (JAMSTEC). and reported 37 species including four spe- Description. —Complete paratypes 64- mm mm cies ofthe genus Nicomache. Intact speci- 151 long, 1.7-2.8 wide, with 31- mm mens are required for the identification of 35setigers(Table 1). Holotype 187 long, mm maldanids because of the morphological 3.5 wide including parapodia, with 32 importance ofthe posteriorbody region. In setigers; with a single achaetous preanal 1 160 PROCEEDINGSOFTHEBIOLOGICALSOCIETY OFWASHINGTON Table 1.—Measurementoftype specimensofNicomacheohtai, new species. Numberofsetigers Numberofanal Specimennumber (achaetousrings) papillae Bodylength(mm) Bodywidth(mm) Dive 450 1 (Holotype) 32(+1) 22 187 3.5 female 2 32(+1) 23 125 2.8 female 3 32(+1) 18 120 2.4 ? 4 32(+1) 25 110 2.2 male 5 32(+2) 24 151 2.6 male 6 35 (+0) 20 130 2.3 ? 7 31 (+1) 18 139 2.5 ? 8 33 (+0) 21 104 2.3 ? Dive 45 1 31 (+1) 23 93 2.8 male D3K 1 32(+1) 19 64 1.7 ? 2* 25+ 25 72 2.0 ? n 10 10 10 11** X 32.2 21.3 122.3 2.46 SD 1.1 2.5 33.5 0.47 *With regeneratedcaudal end. "*SpecimenD3KNo. 2 included. glandularringwellstainedbyMethylGreen. side and several subrostral fibrils (Fig. 2b). Color in alcohol pale, with slightly dark Notopodia with stout bilimbate capillaries brown to reddish brown swollen areas on (Fig. 2d)andshortthinspinulosecapillaries anterior and posterior segments. (Fig. 2c) on all setigers; with spirally spi- Prostomium broadly rounded anteriorly; nulose capillaries (Fig. 2e) and a few short cephalic keel well defined, arched; nuchal slender wavy capillaries (V2 length ofstout slits situated on both sides ofkeel, curved, capillaries) on median and posterior noto- diverging anteriorly; mouth rounded, with podia (Fig. 2g). thick lip (Fig. la, b). Tubecoveredwithcoarsesandgrainsand Setigers 1-6 slightly longer than wide, mud. flaring anteriorly, without collars (Fig. Ic); Variation.—T\iQ total number ofsetigers mediansegmentsverylong,sometimesmore varies from 31 to 35 (X= 32.2) in 10 com- than 4 times longerthan wide; posterior se- plete specimens, with 6 having 32 (Table tigersshort,withwell-definedglandularpads 1). In an exceptional paratype (Dive 450, (Fig. Id, e). Pygidium with dorsally short- No. 6) with 35 setigers, the last setigerous ened anal fiinnel bearing 22 papillae (Fig. segment is merely recognized by the pres- Id-f). enceofitsrightparapodium.Thusthenum- Parapodia biramous; first 3 neuropodia ber is rather constant in the species. with2-6stoutacicularspines(Fig. 2a,Table Some early authors mentioned the num- 2); fiDllowingneuropodiawith 9-12 rostrate ber ofpreanal segments (glandular pads or unciniinanterior2 andposterior 5 setigers, rings) as an important character (e.g., Ima- with 13-19 in middle 25 setigers (Fig. 3). jima & Shiraki 1982: the key to the species Each uncinus with 3-4 teeth above main ofthegenusNicomache),howeverthenum- fang, numerous accessory spines on convex berisvariable(0-2)inthisnewspecies. The VOLUME NUMBER 104, 1 161 a,b 3mm c-f 4mm Fig. 1. Nicomacheohtai(Holotype):a,Anteriorend,dorsalview;b.Same,ventralview;c,Anteriorsegments, lateralview; d. Posteriorsegments, dorsal view; e, Same, lateralview; f, Pygidium, posteriorview. number of papillae on anal funnel ranges per parapodium in 1 1 specimens are 3.5, from 18 to 25 (^= 21.3, « = 10), with each 4.1 and 5.2 on setigers 1, 2 and 3, respec- papilla being very broad and sometimes tively. The number ofanterior setae seems subdivided. to depend on the body size, however only The number of anterior acicular spines the correlation of the number of rostrate perparapodium ranges from 2to 7 with the uncini on parapodium 4L with the body majorityfrom 3 to 6 (Table 2). The number width is significant {R = 0.87, P < 0.001). increases in the three succeeding setigers. Biology.—On some posterior segments, Forexample, theaveragenumbersofspines the spirally spinulose capillaries were cov- 162 PROCEEDINGSOFTHEBIOLOGICALSOCIETYOFWASHINGTON Fig.2. Nicomacheohtai(Holotype):a,Acicularspineonsetiger 1;b.Rostrateuncinus;c,Spinulosecapillary; d,Bilimbatecapillary;e.Distalendofspirallyspinulosecapillary;f,PartofsamewithBeggiatoa-likefilaments; g. Shortwavycapillary. ered with numerous filaments (Fig. 2f), re- lomofmid-posteriorsegments.Theoocytes callingtheBeggiatoa-MkQbacteriafoundon are discoidal or hexagonal with the largest somealvinellidpolychaetesoronsediments measuring about 150 t^m x 50 ixm. of deep-sea hydrothermal vents (Desbru- Remarks.—In the genus Nicomache, 23 yeres et al. 1985, Tunnicliffe et al. 1985). nominal species are recognized (Hartman Femalespecimenshadoocytesinthecoe- 1959, Fauchald 1977, Blake 1985, Blake & VOLUME NUMBER 104, 1 163 • o • •• •••• 13 • • h '' • • • • • • • • • • • • • • • LU • • • • CD • • • • Z • JL ^-- > i 1 « 10 15 20 25 30 SETIGER NUMBER Fig. 3. Distributionofrostrate uncini in the holotype ofNicomacheohtai, new species. Hilbig 1990). Most have 23 setigers or less up to 6 acicular spines in each ofthe first 3 andareeasilydistinguishable from A^. ohtai setigers. A^. ohtai differs from A^. venticola which has more than 30 setigers. Two spe- in having up to 19 rostrate uncini with 3- cies have been described from deep-sea hy- 4 apical teeth in each neuropodium instead drothermalvents:A^. arwidssoniBlake, 1985 ofup to 10 uncini with 2-3 teeth and in the and N. venticola Blake & Hilbig, 1990. A^. presence ofthe shortwavycapillaryinstead ohtaiis most similartoA^. venticola in hav- ofthe absence. The absence ofthe long fil- ing30 ormoresetigers, 22 analpapillaeand amentouscapillaryinthetwohydrothermal Table2.—Distributionofacicularspinesandrostrateuncini(parenthesizednumbers)on firstfoursetigersin type specimensofNicomacheohtai, new species. Setigernumber Specimen number 3L Dive 450 1 2 (10) (9) 2 4 (9) (7) 3 3 (7) (6) 4 3 (7) (7) 5 3 (8) (8) 6 4 (8) (6) 7 4 (8) (10) 8 4 (7) (7) Dive451 1 4 (7) (7) D3K 1 4 (6) (6) 2 3 (6) (6) n 11 11 11 11 11 11 11 11 X 3.5 3.5 4.4 3.9 5.3 5.2 7.5 7.2 SD 0.7 0.7 0.7 0.8 1.0 0.9 1.2 1.3 — PROCEEDINGSOFTHEBIOLOGICALSOCIETY OFWASHINGTON 164 ventspecieswasconsideredasanimportant Nereididae, Glyceridae, Dorvilleidae. Orvini- character for separating them from other idae, andMaldanidae. Pp. 67-101 in Meredith & L.Jones,ed.,Hydrothermalventsoftheeastern congeners (Blake 1985, Blake Hilbig Pacific:anoverview.—BulletinoftheBiological 1990). The presence ofthe short wavy cap- Society ofWashington 6:1-566. illary in N. ohtai is therefore thought to be & B. Hilbig. 1990. Polychaeta from the vi- an intermediate state between these two cinity of deep-sea hydrothermal vents in the groups ofspecies. easternPacific.II:Newspeciesandrecordsfro—m theJuandeFucaandExplorerRidgesystems. Nicomache mossambicaDay, 1951 isan- Pacific Science 44:219-253. other known species with more than 30 se- Day,J. H. 1951. ThepolychaetefaunaofSouthAf- tigers. Both A^. mossambica and A^. ohtai rica. Part 1: The intertidal and estuarine poly- have two or more acicular spines on the chaeta ofNatal and Mocambique.—Annals of fanutnenreiloorftthherefeorsmeetirgeisrsc,ylihnodwreicvaelrantdhedifafnearls Desbruyt1eh9re8e5Ns.a,taDP.lo,lMyFuc.hsGaeaeiutlomlu,s1L2.a:n1Ln-ae6ul7bi.idesr,fr&omY.hyFdoruoqtuheetr.- from the dorsally shortened funnel of the mal vent ecosystems: an ecological overview. latter. Pp. 103-116 inMeredithL. Jones, ed., Hydro- Etymology.—The species is named in thermal vents ofthe eastern Pacific: an over- honorofDr. S. Ohtaofthe Ocean Research view.—Bulletin of the Biological Society of Washington 6:1-566. Institute, University ofTokyo forhis valu- Fauchald, K. 1977. The polychaete worms. Defini- able advice on the sampling using sub- tions and keys to the orders, families and gen- mersibles. era.—Natural History Museum ofLos Angeles County, Science Series 28:1-190. Hartman, O. 1959. Catalogue of the polychaetous Acknowledgments annelids ofthe world. Part 2.—Allan Hancock The authors wish to thankthe staffofthe FoundationPublications,OccasionalPaper23: 355-628. JapanMarineScienceandTechnologyCen- Imajima, M., & Y. Shiraki. 1982. Maldanidae (An- terfortheirassistanceinsamplingonDives nelida:Polychaeta)fromJapan.—Bulletinofthe 450 and 451 ofShinkai 2000 and a dive of NationalScience Museum, Tokyo 8A:7-88. the unmanned submersible D3K. The Laubier,L., S.Ohta,&M. Sibuet. 1986. Decouverte manuscript benefited from the careful re- dceamcpoamgmnuenfaruatnecos-jaanpiomnaaliesseKprAoIfoKnOdedsedpulroanngteelsa view by Dr. James A. Blake, Science Ap- dans les fosses de subduction autour du Ja- plication InternationalCorporation. Partof pon.—ComptesRendusde1'AcademicdesSci- this study was supported by a grant-in-aid ences, Paris, Serie III 303:25-29. from Itoh Science Foundation. Malmgren, A. J. 1865. Nordiska Hafs-Annulater. Ofversigt af Kongl Vetenskaps-Akademiens Forhandlingar 21:51-110 & 181-192, 8 pis. Literature Cited Miura,T. 1988a. ParasiticanimalscollectedinaCa- lyptogena-dominantcommunitydevelopingoff Arwidsson, I. 1907. Studien iiber die skandinavis- Hatsushima, Sagami Bay.—Japan Marine Sci- chen und arkischen Maldaniden nebst Zusam- enceandTechnologyCenter,TechnicalReports menstellung der iibrigen bischer Arten dieser 4:239-244 (inJapanese). Familie.—ZoologischeJahrbiicher,Supplement . 1988b. A new species ofthe genus Proto- 9:1-308, 12, pis. mystides(Annelida,Polychaeta)associatedwith . 1911a. On some Irish Maldanidae.—Pro- a vestimentiferan worm from the Hatsushima ceedingsoftheRoyalIrishAcademy 29B:209- cold-seepsite.—ProceedingsoftheJapaneseSo- 228, 3 pis. cietyofSystematicZoology 38:10-14. . 1911b. DieMaldaniden.—Wissenschaftliche & L. Laubier. 1989. Nautilina calyptogeni- Ergebnisse der Schwedischen Siidpolar-Expe- cola, anewgenusandspeciesofparasiticpoly- dition 1901-1903 6(6):1-44, 2 pis. chaete on a vesicomyid bivalve from Japan Blake, J. A. 1985. Polychaeta from the vicinity of Trench, representative ofa new family Nautil- deep-seageothermalventsintheeasternPacific. inidae.—Zoological Science 6:387-390. & I: Euphrosinidae, Phyllodocidae, Hesionidae, . 1990. Nautiliniellid polychaetes VOLUME NUMBER 104, 1 165 collectedfromtheHatsushimacold-seepsitein (TM) Faculty of Fisheries, Kagoshima Sagami Bay, with descriptions of new genera University, 4-50-20 Shimoarata, Kagoshi- TunnicliafnTde,sVp.e,ciS.esK..—JZuonoilpoegri,ca&lMS.ciEe.ncdeeB7u:r3g1h9.-32159.85. ma 890; (JH) Japan Marine Science and The hydrothermal vent community on axial Technology Center, 2-15 Natsushima-cho, seamount,JuandeFucaRidge. Pp. 453-464 in Yokosuka 237, Japan. Meredith L. Jones, ed., Hydrothermal vents of the eastern Pacific: an overview.—Bulletin of theBiological SocietyofWashington 6:1-566.

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