TOHRU NARUSE. Abstract. Introduction

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Zootaxa : 57 64 (2005) www.mapress.com/zootaxa/ Copyright 2005 Magnolia Press ISSN 1175-5326 (print edition) ZOOTAXA ISSN 1175-5334 (online edition) Species of Moguai Tan and Ng, 1999 (Decapoda: Brachyura: Camptandriidae) from brackish waters in the Ryukyu Islands, Japan, with the description of a new species TOHRU NARUSE The 21st Century COE Program, Graduate School of Engineering and Science, University of the Ryukyus, Senbaru 1, Nishihara, Okinawa 903-0213, and Kuroshima Research Station, Sea Turtle Association of Japan, Kuroshima 136, Taketomi, Okinawa 907-1311, Japan (naruse@southernx.ne.jp) Abstract Two species of Moguai Tan & Ng, 1999 (Camptandriidae) are recorded from the Ryukyu Islands, Japan, one of which is new to science. Moguai pyriforme, sp. nov. is distinguished from other two congeners by its narrower front and the anterolateral margin being located inside the branchial region. Moguai elongatum is recorded from Japan for the first time, and its geographical distribution extended east from Fukien Province, China. A key to the species of Moguai is provided. Key words: Moguai pyriforme, sp. nov., M. elongatum (Rathbun, 1931), Camptandriidae, taxonomy, Ryukyu Islands Introduction The family Camptandriidae contains 20 genera 39 species from West Africa, South Africa, and Madagascar to Sakhalin and New Caledonia, all species occur in marine to estuarine and mangrove habitats. (Barnard, 1955; Guinot & Crosnier, 1963; Manning & Holthuis, 1981; Tan & Ng, 1999; Labai, 2004). The family has long been a subfamily of Ocypodidae or even part of the Macrophthalminae, but it has now been recognised as a distinct family (Harminto & Ng, 1991; Ng, 1998). The camptandriid genus Moguai Tan and Ng, 1999, was described on the basis of only two species, M. aloutos Tan & Ng, 1999, from Singapore and Bintan Island (Indonesia), and M. elongatum (Rathbun, 1931), from Liuwutien (Fukien Province), Hong Kong and Hainan, China (Tan & Ng 1999, Rathbun 1931, Shen 1940). Two species of Moguai were Accepted by P. Castro.: 22 Jul. 2005; published: 2 Sept. 2005 57

ZOOTAXA recently collected from Okinawa, Amami-Oshima, and Ishigaki islands, Japan, one of which is new to science. Materials and Methods Specimens are deposited in the Osaka Museum of Natural History, Osaka, Japan (OMNH), Ryukyu University Museum, Fujukan, Okinawa, Japan (RUMF), and Zoological Reference Collection, Raffles Museum of Biodiversity Research, National University of Singapore, Singapore (ZRC). Specimens were measured using a stereomicroscope (Nikon SMZ-10) provided with an eye-piece micrometer or using a digital slide-caliper (Mitsutoyo CD-20PM) to the nearest 0.1mm. The abbreviation CL is used for the carapace length. The terminology follows Tan & Ng (1999). Taxonomy Camptandriidae Stimpson, 1858 Moguai Tan & Ng, 1999 Moguai pyriforme sp. nov. (Figs. 1a, 2) Moguai elongatum Kishino et al., 2001a: 21, pl. 2 (6); 2001b: 129. Moguai sp. Naruse, 2005 (in press): 207, pl. (Crustacea: lower left). Material examined. Female holotype. CL 5.0 mm, RUMF-ZC-31, Tima River, Okinawa I., coll. T. Naruse, 8 Dec. 2004. Paratypes. 1 female, CL 4.1 mm, ZRC 2005.0111, Tima River, Okinawa, coll. T. Naruse, 25 Dec. 2004; 1 ovigerous female, CL 5.5 mm, OMNH-Ar. 4910, Nakaganeku River, Konase, Amami-Oshima I., coll. T. Kishino, 1 May 2000. Comparative material. Moguai aloutos Tan & Ng, 1999: male paratype, ZRC 1965.7.9.21, Kuantan, Pahang, Peninsular Malaysia, coll. R. Serène; female paratype, ZRC 1997.0357, Lim Chu Kang mangroves, Singapore, coll. C. G. S. Tan, 6 Mar. 1996; 1 male, 13 females, ZRC 1965.7.15.35 44, Kuantan Pahang, Sep. 1935; 5 males, 5 females, ZRC 2003.0339, mangrove, Pulau Bintan, Indonesia, coll. P. K. L. Ng. Description of female holotype. Carapace (Figs. 1a, 2a, b) pear-shaped, 1.05 1.12 times longer than broad, dorsal surface uneven, with ridges, protuberances marginally covered with dark, stiff setae, other areas on carapace with fine, soft setae. Epigastric crista present, each mesogastric, cardiac region with a cross-shaped protuberance, mesobranchial region with anterior outer, median protuberances. Frontal region sloped toward midline, outer margin, frontal margin bilobed in dorsal view, frontal width about third fronto-orbital width; supraorbital margin 58 2005 Magnolia Press NARUSE

rimmed; infraorbital margin with rounded deep excavation, inner edge of excavation fused with suborbital crista, forming infraorbital cup (Fig. 2b); epistome with concave median portion. External orbital angle acute, anterolateral margin without epibranchial tooth, slightly concave, reaching posteriorly about anterior third of carapace, inside lateral wall of epibranchial region; branchial region swollen laterally, posterolateral margin rimmed, rough, continuing from below anterolateral margins to posteriorly produced posterolateral angle. ZOOTAXA FIGURE 1 Moguai pyriforme, sp. nov. and M. elongatum (Rathbun, 1931). a, M. pyriforme, Holotype, female, RUMF-ZC-31, CL 5.0 mm; b, M. elongatum, female, RUMF-ZC-33, CL 5.1 mm Third maxilliped (Fig. 2c) rectangular, without median hiatus between inner margins when closed; exopod tapered distally, reaching distal outer angle of merus, with distinct flagellum; ischium and merus fused, with suture discernible only along the inner third; carpus triangular, anterior apex positioned (in situ) below inner anterior angle of merus. Chelipeds (Fig. 2d) feeble, symmetrical, fingers of chela flat, incurved distally. Ambulatory legs (Fig. 2e) short; meri slightly bent posteriorly, distal posterior angle with blunt projection, dorsal surface with few patches of black, short setae along midline; anterior, posterior margins with long plumose setae; carpi, propodi, dactyli, feeble, dactyli simple, incurved, tip acute, as long as or longer than propodi. Abdomen (Fig. 2f) wide, third to fifth segments fused; first, second segments with transverse ridges along distal margins, fused segments with a medial, pair of lateral transverse ridges on proximal third portion, pair of transverse, one longitudinal ridge on distal half. Male unknown. Variations. A female paratype (ZRC 2005.0111) has one small epibranchial tooth behind the external orbital angle and a mesobranchial region that is relatively narrow than in holotype. MOGUAI 2005 Magnolia Press 59

ZOOTAXA FIGURE 2 Moguai pyriforme, sp. nov. Holotype, female, RUMF-ZC-31, CL 5.0 mm. a, carapace, dorsal view (setae were removed at right half); b, carapace, frontal view; c, third maxilliped, left; d, chela, right; e, third ambulatory leg, left; f, abdomen and telson. Scales, 1 mm. 60 2005 Magnolia Press NARUSE

Habitat. Moguai pyriforme was collected from brackish water on a pebbly-muddy substratum in riverbeds. Distribution. Okinawa and Amami-Oshima islands, central Ryukyu Islands, Japan. Etymology. From the Latin pyriforme meaning pear-shaped, alluding to the shape of the carapace. The name is used as a noun. Remarks. In their revision of Camptandrium Stimpson, 1858, Tan & Ng (1999) established the genus Moguai for a new species, M. aloutos (type species), and Camptandrium elongatum Rathbun, 1931. Moguai was distinguished from Camptandrium by the shape of the carapace being longer than broad, the frontal width being a third the fronto-orbital breadth, the presence of an infraorbital cup (a cup-like protuberance on the infraorbital margin), the distal part of the G1 being bifurcated, the ischium of the third maxilliped not fused with the merus, and the inner distal angle of the ischium of the third maxilliped being acutely produced. Moguai pyriforme differs from the diagnoses provided by Tan & Ng (1999) in that it has a relatively broader front, and the merus and ischium of the third maxilliped are fused. Moguai pyriforme, however, possesses all the other characters that are diagnostic of Moguai, there is no doubt about its generic placement even though no males are available for a description of the G1 structure. The generic definition of the genus Moguai, however, will need to be slightly amended to accommodate the characters of M. pyriforme. Moguai pyriforme can be easily distinguished from M. aloutos and M. elongatum by the proportionately narrower front which is about a third the fronto-orbital breadth (vs. about a half the fronto-orbital breadth), the fusion of the merus and ischium of the third maxilliped (vs. free), and the branchial region being laterally swollen such that the one or two anterolateral teeth are clearly dorsal in position (vs. the branchial region is not distinctly swollen such that the three anterolateral teeth are clearly marginal in position) [cf. Fig. 1b; Tan & Ng 1999: 203, figs. 3, 4; Rathbun 1931: 95, pl. 13(40 43); Shen 1935: 33, figs. 8C, 10]. The degree of swelling of the mesobranchial region is probably a sexually dimorphic character. A large female of M. aloutos (CL 6.2 mm, ZRC 1965.7.15.35 44), has a relatively more swollen mesobranchial region than males, although this is still much less distinct than that observed on M. pyriforme. Kishino et al. (2001a, b) recorded M. elongatum from Amami-Oshima. Their specimen (OMNH-Ar. 4910), however, possesses all the diagnostic characters of M. pyriforme [Kishino, et al., 2001a: pl. 2(6)]; the specimen from Amami-Oshima is not M. elongatum but M. pyriforme. ZOOTAXA Moguai elongatum (Rathbun, 1931) (Fig. 1b) Camptandrium elongatum Rathbun 1931: 95, pl. 13, figs. 40 43; Shen 1935: 33, fig. 10A C; 1940a: 73, 93; 1940b: 234; Shen & Dai 1964: 115; Manning & Holthuis 1981: 199; Dai et al. MOGUAI 2005 Magnolia Press 61

ZOOTAXA 1986: 439, fig. 246; Dai & Yang 1991: 482, pl. 61(3), fig. 246(1). Moguai elongatum Tan & Ng 1999: 205, figs. 3C, D, G, 4D, E. Material examined. 1 male, CL 2.8 mm, 2 females, CL 2.3, 3.2 mm, RUMF-ZC-32, Motonagura, Ishigaki I., coll. T. Naruse & T. Nagai, 21 Dec. 2004; 1 female, CL 5.1 mm, RUMF-ZC-33, Motonagura, Ishigaki I., coll. T. Naruse & T. Nagai, 20 Mar. 2005. Remarks. The specimens from Ishigaki Island agree well with the description of M. elongatum by Rathbun (1931) and Tan & Ng (1999). The range of this species is extended east from Fukien Province, China. Shokita (1990) had recorded M. elongatum from Iriomote I., which is located less than 20 km west of Ishigaki I., but he did not provide a description or figure. Shokitaís (1990) material is almost certainly lost (S. Shokita, pers. comm.), and as such, the identity of his specimens cannot be determined. Specimens from Ishigaki I. were collected from riverbeds of river mouths, with a pebbly-sandy substratum. The locality is exposed by seawater at high tide. Key to species of Moguai 1 Front narrower, width ca. one- third of fronto-orbital breadth......moguai pyriforme, sp. nov. - Front wider, width ca. half of fronto-orbital breadth... 2 2 Supraorbital margin produced dorsally to forming eave in frontal view; posterolateral angle of carapace distinctly produced posteriorly M. aloutos Tan & Ng, 1999 - Supraorbital margin not produced dorsally in frontal view; posterolateral angle of carapace obtuse, being barely produced...m. elongatum (Rathbun, 1931) Acknowledgements We are grateful to Drs. Peter Castro (California State Polytechnic University) and Peter K. L. Ng (National University of Singapore) for their valuable comments, which have improved the paper greatly. The author thanks Prof. Shigemitsu Shokita (University of the Ryukyus) for allowing the use facilities, Drs. Peter K. L. Ng and Tan Swee Hee (Raffles Museum of Biodiversity Research, National University of Singapore) for their help during a stay in Singapore, Dr. Takashi Nagai (University of the Ryukyus) for help in field work, Drs. Tei Kishino (River Ecological Research, Kyoto) and Hsi-Te Shih (National Chung- Hsing University, Taichung) for providing literature, and Dr. Ryohei Yamanishi (Osaka Museum of Natural History) for the loan of specimens. This study was supported by the 21st Century COE program of the University of the Ryukyus. 62 2005 Magnolia Press NARUSE

References Barnard, K. H. (1955) Addition to the fauna-list of South African Crustacea and Pycnogonida. Annals of the South African Museum, 43, 1 107. Dai, A.-Y. & Yang, S.-L. (1991) Crabs of the China Seas. Springer-Verlag, Berlin, 608 pp, 74 pls. Dai, A.-Y., Yang, S.-L., Song, Y.-Z. & Chen, G.-X. (1986) Crabs of the China Seas. China Ocean Press, Beijing, 11+642 pp. [in Chinese] Guinot, D. & Crosnier, A. (1963) Remarques sur les genres Cleistostoma, Paracleistostoma et Tylodiplax et description de Tylodiplax derijardi sp. nov. (Crust. Decap. Brachyura). Bulletin du Muséum national d'histoire naturelle, (2)35(6), 606 619. Harminto, S. & Ng, P.K.L. (1991) A revision of the Camptandriinae genus Baruna Stebbing, 1904 (Crustacea: Brachyura: Decapoda: Ocypodidae), with descriptions of two new species from the Indo-West Pacific. Raffles Bulletin of Zoology, 39(1), 187 208. Kishino, T., Yonezawa, T., Nomoto, A., Kimura, S. & Wada, K. (2001a) Twelve rare species of brachyuran crabs recorded in the brackish waters of Amami-Oshima Island, Kagoshima Prefecture, Japan. Nankiseibutsu, 43(1), 15 22. [in Japanese] Kishino, T., Nomoto, A., Kimura, S., Yonezawa, T. & Wada, K. (2001b) Brachyuran crab species recorded in the brackish waters of Amami-Oshima Island, Kagoshima Prefecture, Japan. Nankiseibutsu, 43(2), 125 131. [in Japanese] Labai, V.S. (2004) Paracleistostoma cristatum De Man, 1895 (Crustacea: Decapoda), a crab species new for the fauna of Russia from the estuarine waters of the south Sakhalin. Russian Journal of Marine Biology, 30(1), 56 60. Manning, R. B. & Holthuis, L. B. (1981) West African brachyuran crabs (Crustacea: Decapoda). Smithsonian Contributions to Zoology, 306, 1 379. Naruse, T. (2005 in press). Moguai sp. In Nature Conservation Division, Department of Cultural & Environmental Affairs, Okinawa Prefectural Government (Ed.) Threatened Wildlife in Okinawa, 2nd ed. (Animals) Red Data Okinawa. Nature Conservation Division, Department of Cultural & Environmental Affairs, Okinawa Prefectural Government, Okinawa, pp. 207 208, pl. (Crustacea: lower left). [in Japanese] Ng, P.K.L. (1998) Crabs. In: Carpenter K.E. & Niem V.H. (eds.) FAO Species Identification Guide for Fishery Purposes. The Living Marine Resources of the Western Central Pacific. Volume 2. Cephalopods, Crustaceans, Holothurians and Sharks. Food and Agriculture Organisation, Rome, pp. 1045 1155. Rathbun, M. J. (1931) New and rare Chinese crabs. Lingnan Science Journal, (1929), 75 125. Shen, C.-J. (1935) On some new and rare crabs of the families Pinnotheridae, Grapsidae and Ocypodidae from China. Chinese Journal of Zoology, 1, 19 40, 15 figs. Shen, C.-J. (1940a) On the collection of crabs of South China. Bulletin of the Fan Memorial Institute of Biology (Zoology), 10(2), 69 103. Shen, C.-J. (1940b) The brachyuran fauna of Hong Kong. Journal of the Hong Kong Fisheries Research Station, 1(2), 211 242. Shen, C.-J. & Dai, A.-Y. (1964) Illustrations of Animals in China (Crustacea, part II). Science Press, Beijing, 142 pp. [in Chinese] Shokita, S. (1990) Inland-water decapods and their distribution in Iriomote Island of the Ryukyu Islands. In: Nature Conservation Bureau, Environment Agency (Ed.), Study of Essential Factors for Preservation of Wildlife in Nansei Islands. Conservation Bureau, Environment Agency, Tokyo, pp 305 317. [in Japanese with English summary and captions] Stimpson, W. (1858) Prodromus descriptionis animalium evertebratorum, quae in Expeditione ad Oceanum Pacificum Septentrionalem, a Republica Federate missa, Cadwaladaro Ringgold et Johanne Rodgers Ducibus, observavit et descripsit. Pars V. Crustacea Ocypodoidea. Proceedings of the Academy of Natural Science of Philadelphia, 10, 93 110. ZOOTAXA MOGUAI 2005 Magnolia Press 63

ZOOTAXA Tan, C.G.S. & Ng, P.K.L. (1999) A revision of the genus Camptandrium Stimpson, 1858 (Crustacea: Decapoda: Brachyura: Camptandriidae). Raffles Bulletin of Zoology, 47(1), 193 219. 64 2005 Magnolia Press NARUSE