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Deep-sea Galatheidae (Crustacea, Decapoda, Anomura) from Tosa Bay and Okinawa Trough, Southern Japan PDF

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Preview Deep-sea Galatheidae (Crustacea, Decapoda, Anomura) from Tosa Bay and Okinawa Trough, Southern Japan

Bull. Natl. Mus. Nat. Sci., Ser. A, 33(4), pp. 133–146, December 21, 2007 Deep-sea Galatheidae (Crustacea, Decapoda, Anomura) from Tosa Bay and Okinawa Trough, Southern Japan Masayuki Osawa1and Masatsune Takeda2,3 1Department of Marine and Environmental Sciences, University of the Ryukyus, 1 Senbaru, Nishihara-cho, Okinawa 903–0213, Japan 2Department of Zoology, National Museum of Nature and Science, 3–23–1, Hyakunincho, Shinjuku-ku, Tokyo 169–0073, Japan 3Faculty of Modern Life, Teikyo Heisei University, 2289–23 Uruido, Ichihara, Chiba 290–0193, Japan Abstract Crustaceans of the family Galatheidae are reported from Tosa Bay and Okinawa Trough, southern Japan, at depths ranging from 526m to 3278m. The material comprises two species of Munida Leach, 1820, two species of Galacantha A. Milne-Edwards, 1880, and nine species of MunidopsisWhiteaves, 1874. Eight of these species are new to the carcinological fauna of Japan: Munida tiresiasMacpherson, 1994, Galacantha bellisHenderson, 1885, Munidopsis an- damanicaMacGilchrist, 1905, M. bairdii(Smith, 1884), M. bispinoculataBaba, 1988, M. centrina Alcock and Anderson, 1894, M. pilosa Henderson 1885, and M. verrilli Benedict, 1902. Brief notes on the decapod crustaceans recorded from abyssal depths of Japanese waters are provided. Key words: Crustacea, Decapoda, Galatheidae, Tosa Bay, Okinawa Trough, new records, abyssal depths. Introduction proximately 80m in the northern Nansei Islands. The research project entitled “Study on Deep- The present paper reports on the Galatheidae Sea Fauna and Conservation of Deep-Sea based on the material of the research project and Ecosystem” has been carried out by the National some additional specimens from Tosa Bay and Science Museum (now National Museum of Na- Okinawa Trough located along the Nansei Is- ture and Science), Tokyo, in southern Japan since lands, southern Japan, at lower bathyal and 1993. Investigations during three phases of the abyssal depths ranging from 526m to 3278m. project were conducted in Suruga Bay on the Pa- The material includes two species of Munida cific coast of central Honshu mainland from Leach, 1820, two species of Galacantha A. 1993 to 1996, Tosa Bay off Shikoku Island from Milne-Edwards, 1880, and nine species of Mu- 1997 to 2000, and the sea around the Nansei nidopsis Whiteaves, 1874. Eight species are new (Ryukyu) Islands from 2001 to 2004, respective- to Japan. ly (Kubodera and Machida, 1997; Saito et al., The specimens examined are deposited in the 2001; Shinohara et al., 2005). Although Takeda National Museum of Nature and Science, Tokyo (1997) reported on the decapod crustaceans, in- (NSMT) and the Natural History Museum and cluding galatheids, from Suruga Bay based on Institute, Chiba (CBM). The size of the speci- the material collected during the research, no mens is indicated by postorbital carapace length reports have been made on the deep-water (cl), which is measured from the orbital margin galatheids from Tosa Bay and the Nansei Islands. (posterior lateral end of the ocular peduncle in Osawa (2006) described only a single species, dorsal view) to the posterior margin of the cara- Galathea patae, from the shallow depth of ap- pace on the dorsal midline. The general terminol- 134 Masayuki Osawa and Masatsune Takeda ogy follows that of Baba (2005). 6.9mm), NSMT-Cr 17836. Remarks. The two specimens examined agree well with the original description and illus- Taxonomy trations of Munida tiresias. In the larger speci- Family Galatheidae men, the first article of the antennal peduncle has Munida parvioculataBaba, 1982 a distomesial spine barely reaching the midlength (Fig. 1A, B) of the second article, and the second article lacks a distomesial spine. In the type material and Munida parvioculataBaba, 1982: 104, figs. 1, 2b. smaller specimen examined, the first antennal ar- Material examined. Tosa Bay: R/V Tansei- ticle possesses a short distomesial spine never Maru, KT00-08, st. BT-6 (32°30.6(cid:1)–32°30.6(cid:1)N, reaching the midlength of the second article and 133°56.3(cid:1)–133°55.4(cid:1)E, 1227–1360m), 26 June a small but distinct distomesial spine is present 2000, beam trawl, 2 males (cl 10.2, 14.1mm), on the second article. NSMT-Cr 17835. Distribution. Previously known only from Remarks. The present specimens agree well New Caledonia, 1140–2049m, and presently with the original description of Munida parvioc- from Japan (Okinawa Trough), 2027–2063m. ulatain the diagnostic respects including that the The present record greatly extends its distribu- lateral margins of the carapace are somewhat tion to the Northern hemisphere. convex with the anterior second lateral spine well developed, and the dactylus of the second pereo- Galacantha bellisHenderson, 1885 pod is approximately half as long as the propo- (Fig. 2A, B) dus. Some minor morphological differences, which could be treated as intraspecific variations, Galacantha bellis Henderson, 1885: 418; Macpherson, 2007: 9 (synonymy and references), figs. 1–4. are found in the present material. The second ab- dominal segment is armed with four or five Material examined. Tosa Bay: R/V Tansei- spines on the anterior transverse ridge, but the Maru,KT00-08, st. BT-9-2 (32°09.3(cid:1)–32°08.9(cid:1)N, original description cites as having only two me- 134°03.4(cid:1)–134°06.0(cid:1)E, 2739–3278m), 26 June dian spines or a tubercular process in addition to 2000, beam trawl, 2 males (cl 13.6, 18.6mm), the two spines. The third article of the antennal 2 females (cl 17.7, 18.1mm), 1 ovigerous peduncle has a minute or small distolateral spine female (cl 19.4mm), NSMT-Cr 17837; R/V in the present specimens unlike in the type mate- Hakuho-Maru, KH02-03, st. TE (32°12.67(cid:1)N, rial. Also the smaller specimen examined is not 133°55.64(cid:1)E, 2445m), 10 September 2002, beam armed with a distomesial spine on the third an- trawl, 1 ovigerous female (cl 19.0mm), NSMT- tennal article, whereas the spine is present in the Cr 17838. larger specimen examined and the type material. Okinawa Trough: R/V Tansei-Maru, KT02-03, Distribution. Known only from Japan: Izu Is- st. C-4 (25°24.47(cid:1)–25°25.03(cid:1)N, 124°57.58(cid:1)– lands and Tosa Bay; 430–1400m. 124°59.41(cid:1)E, 2133–2125m), 24 April 2002, beam trawl, 1 male (cl 14.6mm), NSMT-Cr Munida tiresiasMacpherson, 1994 17839; st. D-2 (1) (27°02.33(cid:1)–27°02.88(cid:1)N, (Fig. 1C, D) 126°58.24(cid:1)–126°59.08(cid:1)E, 1557–1540m), 28 April 2002, beam trawl, 1 ovigerous female (cl Munida tiresiasMacpherson, 1994: 545, fig. 57. 18.7mm), NSMT-Cr 17840. Material examined. Okinawa Trough: R/V Coloration. Carapace, abdomen, and pere- Tansei-Maru, KT02-03, st. A-2 (25°23.16(cid:1)–25° opods entirely light red. 22.28(cid:1)N,127°14.29(cid:1)–127°12.97(cid:1)E, 2027–2063m), Remarks. The present material agrees well 24 April 2002, beam trawl, 2 females (cl 6.1, with the recent description of G. bellis provided Deep-sea Galatheidae from Japan 135 Fig. 1. Dorsal view. A, B, Munida parvioculataBaba, 1982, male (cl 14.1mm), NSMT-Cr 17835, Tosa Bay; C, D, Munida tiresias Macpherson, 1994, female (cl 6.1mm), NSMT-Cr 17836, Okinawa Trough. 136 Masayuki Osawa and Masatsune Takeda Fig. 2. Dorsal view. A, B, Galacantha bellis Henderson, 1885, ovigerous female (cl 18.7mm), NSMT-Cr 17840, Okinawa Trough; C, D, Galacantha valdiviaeBalss, 1913, ovigerous female (cl 15.2mm), NSMT-Cr 17841, Okinawa Trough. Deep-sea Galatheidae from Japan 137 by Macpherson (2007) except that the dorsal Munidopsis andamanicaMacGilchrist, 1905 transverse groove of the fourth abdominal seg- (Fig. 3A, B) ment is interrupted medially in some specimens. Munidopsis Wardeni var. andamanica MacGilchrist, Macpherson (2007) mentioned that the groove is 1905; 245. not interrupted in his specimens of G. bellis and Munidopsis andamanica: Baba, 1988: 140, fig. 53; 2005; the interruption is characteristic of its close rela- 284 (synonymy and references); Macpherson, 2007; tive G. subrostrata Macpherson, 2007 from the 37. northeast Atlantic. However, Macpherson (2007) Material examined. Tosa Bay: R/V Kotaka- also suggested that the morphological variations Maru, K98-12, st. K98-12-600 (33°12.1(cid:1)– observed in his specimens of G. bellis require 33°11.8(cid:1)N, 133°44.4(cid:1)–133°45.4(cid:1)E, 654–686m), further study in order to confirm the existence of 10 December 1998, otter trawl, 1 male (cl 15.0 a single or several species. The Japanese speci- mm), NSMT-Cr 17842; st. K98-12-800 (33° mens can be assigned to G. bellis until further 11.4(cid:1)–33°10.6(cid:1)N,133°53.8(cid:1)–133°55.3(cid:1)E,744–786 detailed study is made. m), 11 December 1998, otter trawl, 1 female (cl Distribution. Madagascar, Bay of Bengal, 14.2mm), NSMT-Cr 17843. Laccadive Sea, Arabian Sea, Sri Lanka, central Remarks. The specimens examined agree Indian Ocean, Makassar Strait (Indonesia), well with the original description and an account Solomon Islands, New Caledonia, Wallis and Fu- provided by Baba (1988). Munidopsis andamani- tuna area, off Valparaiso in Chile, and presently ca is closely allied to M. cylindrops Benedict, Japan (Tosa Bay and Okinawa Trough); 1035– 1902 from Japan and Mindanao Sea, but distin- 3800m. guished by the corneas of the ocular peduncles being cylindrical rather than oval. Distribution. Andaman Sea, west coast of Galacantha valdiviaeBalss, 1913 Sumatra, Indonesia, Philippines, South China (Fig. 2C, D) Sea, Taiwan, Solomon Islands, New Caledonia, Galacantha valdiviae Balss, 1913; 224; Macpherson, Vanuatu and Fiji Islands, and presently Japan 2007; 29 (synonymy and references), figs. 15, 16. (Tosa Bay); 333–1598m. Material examined. Okinawa Trough: R/V Tansei-Maru, KT02-03, st. E-2 (26°15.10(cid:1)–26° Munidopsis antonii(Filhol, 1884) 13.85(cid:1)N, 125°17.22(cid:1)–125°18.43(cid:1)E, 991–955m), (Fig. 3C, D) 26 April 2002, beam trawl, 1 young female (cl 7.3mm), 1 ovigerous female (cl 15.2mm), Galathodes antoniiFilhol, 1884: 230, fig. 2. Munidopsis antonii: Baba, 2005: 132, 284 (synonymy and NSMT-Cr 17841. references), figs. 52–54; Macpherson, 2007: 38. Remarks. The present specimens agree well with the recent diagnosis provided by Macpher- Material examined. South of Tosa Bay: R/V son (2007). No distinct differences are found. Tansei-Maru, KT00-08, st. BT-9-2 (32°09.3(cid:1)– Distribution. Off east coast of Somali Re- 32°08.9(cid:1)N, 134°03.4(cid:1)–134°06.0(cid:1)E, 2739– public, Madagascar, Mozambique Channel, 3278m), 26 June 2000, beam trawl, 1 ovigerous Moluccas, off northwest Sulawesi, Palawan Pas- female (cl 34.4mm), NSMT-Cr 17844. sage, off Kii Peninsula and Okinawa Trough in Remarks. The taxonomy and morphological Japan, off Central Queensland, and Solomon Is- variations of this species are fully discussed by lands; 991–1644m. Baba (2005). Jones and Macpherson (2007) re- cently described Munidopsis segonzaci, a close relative of M. antonii, from off California. Mu- nidopsis segonzaci can be differentiated from M. 138 Masayuki Osawa and Masatsune Takeda Fig. 3. Dorsal view. A, B, Munidopsis andamanica MacGilchrist, 1905, male (cl 15.0mm), NSMT-Cr 17842, Tosa Bay; C, D, Munidopsis antonii (Filhol, 1884), ovigerous female (cl 34.4mm), NSMT-Cr 17844, Tosa Bay. Deep-sea Galatheidae from Japan 139 antonii, which is widely distributed in the world Material examined. Okinawa Trough: R/V oceans, by the shorter rostrum and the eyespine Tansei-Maru, KT02-03, st. C-4 (25°24.47(cid:1)– strongly concave on the mesial margin (straight 25°25.03(cid:1)N, 124°57.58(cid:1)–124°59.41(cid:1)E, 2133– or slightly concave in M. antonii). 2125m), 24 April 2002, beam trawl, 2 males (cl Distribution. Atlantic Ocean—From north- 17.1, 19.6mm), 1 female (cl 17.0mm), NSMT- western Atlantic and Bay of Biscay to off South Cr 17845; st. D-2 (2) (26°30.63(cid:1)N, 127°04.16(cid:1)E, Africa, southeastern Atlantic; Pacific Ocean— 1900–1920m), 17 April 2002, beam trawl, 1 fe- Eastern Pacific from off Oregon to Juan Fernan- male (cl 23.6mm), CBM-ZC 7643. dez, Bering Sea, Japan (Izu Islands and Tosa Remarks. The present specimens show a cer- Bay), off Zamboanga, Tasman Sea; Indian tain variation in the arrangement of the submedi- Ocean—Southwestern Australia, Mozambique, an spines and number of the posterior marginal and off Sri Lanka; 366–458m and 2516–4460m. spines on the carapace, as found in the material reported by Macpherson and Segonzac (2005) and Macpherson (2007). The arrangement of the Munidopsis bairdii(Smith, 1884) submedian spines varies in the three specimens (Fig. 4A, B) as follows: 2-0-2-0-2-1, 2-1-2-2-2-1, 2-2-3-0-3-1, Galacantha bairdiiSmith, 1884: 356. and 2-1-2-0-2-2. Those spines are situated in the Munidopsis bairdii: Baba, 2005: 285 (references); epigastric, protogastric, mesogastric, anterior car- Macpherson and Segonzac, 2005: 17, fig. 4; Macpher- diac (just behind the cervical groove), posterior son, 2007: 43 (synonymy). Fig. 4. Dorsal view. Munidopsis bairdii(Smith, 1884), male (cl 19.6mm) (A), female (cl 17.0mm) (B), NSMT- Cr 17845, Okinawa Trough. 140 Masayuki Osawa and Masatsune Takeda cardiac, and intestinal regions, respectively. The Munidopsis centrina Alcock and Anderson, 1894: 170; specimens examined also have two to five spines Baba, 2005: 139, 286 (synonymy and references), fig. 57; Macpherson, 2007: 49. (two or three median spines, or two median and two or three lateral spines) on the posterior mar- Material examined. South of Tosa Bay: R/V ginal ridge of the carapace. Tansei-Maru, KT00-08, st. BT-9-2 (32°09.3(cid:1)– The specimens examined agree well with the 32°08.9(cid:1) N, 134°03.4(cid:1)–134°06.0(cid:1)E, 2739–3278 diagnosis of M. bairdiinoted by Macpherson and m), 26 June 2000, beam trawl, 1 male (cl 19.1 Segonzac (2005) in every respect including the mm), NSMT-Cr 17847. carapace armed with four distinct spines on each Remarks. The specimen examined generally lateral margin and the eyespine directed straight agrees with the diagnosis recently provided by forward. Baba (2005). The distolateral spine of the first ar- Distribution. Atlantic Ocean—Off Delaware ticle of the antennal peduncle barely reaches the Bay, off New England, Middle Atlantic Bight, distal margin of the second article. The second from off British Isles to Bay of Biscay, west of pereopod terminates at the tip of the first pereo- Cape Point in South Africa; Eastern Pacific— pod. These intraspecific variations are noted in Gulf of Panama, Ecuador, Baja California, off the small “Galathea” specimen by Baba (2005). Oregon; Indian Ocean—Sri Lanka; 1986– Distribution. Madagascar,MozambiqueChan- 4260m. The present specimens represent the first nel, Reunion Island, Bay of Bengal, Tasman Sea, record in the western Pacific (Okinawa Trough, New Caledonia, and presently Japan (Tosa Bay); Japan). 2300–3485m. Munidopsis bispinoculataBaba, 1988 Munidopsis pilosaHenderson, 1885 Munidopsis bispinoculataBaba, 1988: 142, fig. 54; 2005: Munidopsis pilosa Henderson, 1885: 415; Baba, 2005: 137, 285; Baba and Poore, 2002: 232, fig. 1; Macpher- 293 (references); Macpherson, 2007: 93. son, 2007: 44, fig. 55D. Material examined. Tosa Bay: R/V Kotaka- Material examined. Tosa Bay: R/V Kotaka- Maru, K00-08, st. K00-08-800 (32°59.99–33° Maru, K00-08, st. K00-08-800 (32°59.9(cid:1)– 00.3(cid:1)N, 133°37.4(cid:1)–133°37.9(cid:1)E, 820–840m), 23 33°00.3(cid:1)N, 133°37.4(cid:1)–133°37.9(cid:1)E, 820–840m), August 2000, otter trawl, 1 male (cl 9.3mm), 23 August 2000, otter trawl, 1 male (cl 8.5mm), NSMT-Cr 17848. 1 female (cl 12.5mm), NSMT-Cr 17846. Remarks. The diagnosis and detailed illustra- Remarks. As Baba and Poore (2002) and tions of this species are provided by Baba (1988) Baba (2005) noted for their specimens from the on the basis of the “Albatross” material. There southeastern Australia and Mindanao Sea, the are no clear differences in the present specimen. present material also has numerous, weak trans- Distribution. Madagascar, Andaman Sea, In- verse ridges on the carapace and two or four, donesia, Philippines, Solomon Islands, Vanuatu, comparatively small spines on the anterior mar- Tonga Islands, and presently Japan (Tosa Bay); gin of the third thoracic sternite. 732–1640m. Distribution. Madagascar, Philippines, In- donesia, New South Wales, Solomon Islands, Munidopsis subchelataBalss, 1913 Vanuatu, Fiji, and presently Japan (Tosa Bay); 443–2363m. (Fig. 5C, D) Munidopsis subchelataBalss, 1913: 222; Baba, 2005: 296 (synonymy and references); Macpherson, 2007: 110. Munidopsis centrinaAlcock and Anderson, 1894 Material examined. Okinawa Trough: R/V (Fig. 5A, B) Tansei-Maru, KT02-03, st. E-2 (26°15.10(cid:1)– Deep-sea Galatheidae from Japan 141 Fig. 5. Dorsal view. A, B, Munidopsis centrina Alcock and Anderson, 1894, male (cl 19.1mm), NSMT-Cr 17847, Tosa Bay; C, D, Munidopsis subchelataBalss, 1913, male (cl 21.6mm), NSMT-Cr 17849, Okinawa Trough. 142 Masayuki Osawa and Masatsune Takeda 26°13.85(cid:1)N, 125°17.22(cid:1)–125°18.43(cid:1)E, 991–955 12.65(cid:1)N, 124°54.27(cid:1)–124°55.47(cid:1)E, 991–955m), m), 26 April 2002, beam trawl, 1 male (cl 26 April 2002, beam trawl, 1 female (cl 21.6mm), NSMT-Cr 17849. 20.3mm), NSMT-Cr 17851. Remarks. Baba and Williams (1998: 154) Remarks. The sole specimen examined mentioned that Munidopsis plana Baba, 1986, agrees well with the diagnosis recently provided appears to be a junior synonym of the Balss’ by Baba (2005). The fixed finger of the first pere- species. The present specimen obtained from the opod lacks a denticulate carina on the distolateral Okinawa Trough, the type locality of M. plana, margin. The propodus of the second pereopod is agrees well with the type material of this species unarmed on the dorsal surface. as well as M. subchelata in the diagnostic re- Distribution. Eastern Pacific–Off Oregon, spects. San Nicolas Island, Santa Cruz Basin, from Mon- Distribution. West of Sumatra, Makassar terey Bay to off Cerros Island, and off San Diego; Strait, Okinawa Trough in Japan, and Solomon Western Pacific—Makassar Strait, Tasmania, and Islands, at depths of 560–1080m. presently Japan (Okinawa Trough); 732–4169m. Munidopsis trifidaHenderson, 1885 Abyssal galatheids and other decapod (Fig. 6A, B) crustaceans from Japanese waters Munidopsis trifidaHenderson, 1885: 415; Baba, 2005: Only two galatheid species, Munidopsis an- 193, 298 (synonymy and references); Macpherson, 2007: tonii and M. subsquamosa Henderson, 1885, 115. have been recorded from Japanese waters at Material examined. Tosa Bay: R/V Kotaka- abyssal depths of over 3000m (Baba, 1982, Maru, K99-03, st. K99-03-500 (33°12.5(cid:1)– 2005). The present material contains two species, 33°11.7(cid:1)N, 133°41.9(cid:1)–133°41.4(cid:1)E, 526–539m), Galacantha bellis and M. centrina, as additions 3 March 1999, otter trawl, 2 males (cl 17.3, 17.6 to Japanese abyssal galatheid fauna. mm), NSMT-Cr 17850. Osawa et al. (2006) reported four Munidopsis Remarks. The specimens examined have the species, M. panamae Baba, 2005, M. profunda body and pereopods covered with fine setae and Baba, 2005, M. tafrii Osawa, Lin and Chan, the palm of the first pereopod unarmed on the 2006, and M. teretis Baba, 2005, from depths of mesial margin. These characters agree with the 3564–4455m off Taiwan, which is adjacent to observations of the western Pacific material by Japanese waters. Examination of the material Baba (1969, 2005) and Macpherson (2007). newly obtained during the recent research cruises Distribution. Madagascar, Laccadive Sea, around Taiwan has revealed the presence of sev- southern Arabian coast, Gulf of Aden, Bay of eral additional Munidopsis species from abyssal Bengal, Indonesia, South and East China Seas, depths (Osawa et al., in press). Among the four Okinawa Trough, Suruga Bay, Sagami Bay, species recorded from Japanese abyssal depths, Solomon Islands, New Caledonia, Straits of only M. centrinais found in the Taiwanese mate- Magellan, and south of Chile; 280–1270m. rial. The other three species have been known from the eastern and western Pacific and even from Indian Ocean or Atlantic Ocean (Baba, Munidopsis verrilliBenedict, 1902 2005; Macpherson, 2007). Thus the apparent dif- (Fig. 6C, D) ferences between the faunas of Japan and Taiwan Munidopsis verrilli Benedict, 1902: 291, fig. 34; Baba, may simply reflect the differences of sampling 2005: 194, 298 (references). effort or technical difficulties in collecting partic- Material examined. Okinawa Trough: R/V ular species. Tansei-Maru, KT02-03, st. E-1 (26°11.34(cid:1)–26° Besides these galatheids, only seven decapod

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