Stiphodon annieae, a new species of freshwater goby from Indonesia (Gobiidae)

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Stiphodon annieae, a new species of freshwater goby from Indonesia (Gobiidae) by Philippe Keith * (1) & Renny K. Hadiaty (2) Abstract. Stiphodon annieae, new species, is described on the basis of material collected from Halmahera (Indonesia). It is distinguished from all other congeners in having a bright blue and red color pattern in males, nine segmented rays in the second dorsal fin, 14 pectoral rays, 34-40 fine tricuspid premaxillary teeth, and a large head. SFI Received: 27 Mar. 2014 Accepted: 5 Sep. 2014 Editor: R. Causse Key words Gobiidae Stiphodon annieae Indonesia Halmahera Freshwater New species Résumé. Stiphodon annieae, une espèce nouvelle de gobie d eau douce d Indonésie (Gobiidae). Stiphodon annieae, espèce nouvelle, est décrite à partir de matériel collecté à Halmahera (Indonésie). Elle se distingue des autres espèces du genre par les couleurs brillantes rouge et bleue du mâle, par neuf rayons segmentés à la seconde nageoire dorsale, 14 rayons aux nageoires pectorales, 34 à 40 dents prémaxillaires tricuspides et une grande tête. During the past 35 years numerous sicydiine gobies have been collected and identified from freshwater streams throughout the tropical Indo-Pacific. Nevertheless, many islands of this region are undersampled (Watson, 1996; Watson et al., 2007; Keith et al., 2010; Thuesen et al., 2011). Recently, a number of expeditions led by the Indonesian Institute of Sciences (LIPI) into remote areas of Indonesia and in collaboration with the Institute for Research and Development (IRD) and the National Museum of Natural History of Paris (MNHN), resulted in the discovery of further new species (Keith et al., 2011a; Pouyaud et al., 2012; Keith et al., 2012). Compared to other sicydiine genera, Stiphodon are unique among the Sicydiinae in having three anal pterygiophores anterior to the first haemal spine (Birdsong et al., 1988); in all the other genera belonging to the group, there are only two. Stiphodon possesses tricuspid premaxillary teeth in both sexes. The ascending process on the premaxilla is narrow at the dorsal tip. The tongue is fused to floor of the mouth. The pelvic disc is adherent to the belly between fifth rays only and there are 13-17 pectoral rays (Keith and Marquet, 2007; Keith and Lord, 2011a; Maeda et al., 2011). Taillebois et al. (2014) suggested that Stiphodon may be the sister group of all other Sicydiinae species, based on molecular evidence. Stiphodon currently contains nearly 30 species, and is distributed from southern Japan, Indonesia and Sri Lanka to New Caledonia and French Polynesia (Keith et al., 2002; Watson et al., 2005; Keith et al., 2007; Keith et al., 2009; Keith et al., 2011b; Maeda and Tan, 2013; Maeda, 2014). The purpose of this paper is to provide a description of a new Stiphodon known from Halmahera (Indonesia). Methods Methods follow Keith and Marquet (2007). Measurements were taken with a dial caliper to the nearest tenth of a millimeter. All counts were taken from the right side. The size is given as standard length (SL). Teeth were counted to the right of the premaxillary symphysis. Abbreviations for institutions and collections cited follow Leviton et al. (1985). Abbreviations for the cephalic sensory pore system follow Akihito (1986). Scale and fin ray counts are reported as: A, anal fin elements (includes flexible spine and segmented rays); D, dorsal fins (D1, first dorsal fin spines; D2, second dorsal fin elements); P, pectoral fin rays; C, caudal fin rays (only branched rays are reported); LS, scales in lateral series counted from upper pectora1 fin base, or anteriormost scale along lateral midline, to central hypural base; PD, predorsal midline scales counted from scale directly anterior to first dorsal fin insertion to the anteriormost scale; TRB, transverse series backward, refers to scales counted from the first scale anterior to second dorsal fin origin, in a diagonal manner, posteriorly (1) Muséum national d Histoire naturelle, UMR 7208 (MNHN-CNRS-UPMC-IRD-UCBN), DMPA, CP 026, 43, rue Cuvier, F-75231 Paris cedex 05, France. (2) LIPI, Zoology Division, MZB, Gedung Widyasatwaloka, Jl. Raya Jakarta Bogor Km. 46, Cibinong- Bogor 16911, Indonesia. [renny_hadiaty@yahoo.com] * Corresponding author [keith@mnhn.fr] Cybium 2014, 38(4): 267-272.

Stiphodon anniaeae, a new species of goby from Indonesia Keith & Hadiaty Figure 1. - Stiphodon annieae n. sp., Holotype, MZB 18930, male (21.5 mm SL), Hamahera, Indonesia; Hadiaty et al. coll. (Photo R. Hadiaty). and ventrally to the anal fin base or ventralmost scale; TRF, transverse series forward, refers to scales counted from the first scale anterior to second dorsal fin origin, in a diagonal manner, anteriorly and ventrally to the centre of abdomen or ventralmost scale; ZZ, zigzag series, refers to scales on the narrowest region of the caudal peduncle counted from the dorsalmost scale to the ventralmost scale in a zigzag (alternating) manner. Holotype. MZB 18930, male (21.5 mm SL), S. Wosea, DS. Sawai, Weda Tengah, Halmahera, Maluku, Indonesia; 22 Jan. 2010, Hadiaty, Wowor and Sopian coll. Paratype. MNHN 2014-0132, male (22.7 mm SL), same data as holotype. Stiphodon annieae, n. sp. (Figs 1-2, Tabs I-III) Comparative material The new species is compared in text and tables with species having 13-14 pectoral rays, nine segmented rays in the second dorsal fin, and a red color pattern in males (bright red on body sides and part of fins). These are Stiphodon rubromaculatus Keith & Marquet, 2007, S. birdsong Watson, 1996, S. surrufus Watson & Kottelat, 1995 and S. mele Keith, Marquet & Pouilly, 2009. Stiphodon mele Keith, Marquet & Pouilly, 2009. Holotype: MNHN 2008-1920, male (27.2 mm SL), Efate, Mele waterfall, 22 Jul. 2002,Vanuatu. Keith and Keith coll. Paratypes: MNHN 2008-1921, one male (21.1 mm SL), Gaua, Solomul River, 21 Jul. 2005, Vanuatu. Keith, Marquet and Keith coll. MNHN 2008-1922, two males, one female (21.1-25.3 mm SL), Santo, Patunar s Doline, Vanuatu, 14 Sep. 2006. Pouilly coll. MNHN 2008-1923, one female, (23.8 mm SL), Santo, Patunar resurgence, Vanuatu, 15 Sep. 2006. Pouilly coll. MNHN 2008-1924, one male, New Caledonia, North Province (26.2 mm SL). Keith et al. coll. Material for S. rubromaculatus, S. birdsong and S. surrufus, is that listed in Keith and Marquet (2007). Material examined Two males collected from Halmahera (Indonesia) with a size range of 21.5-22.7 mm SL. Figure 2. - Diagrammatic illustration of head in Stiphodon annieae n. sp. (male) showing head pores and sensory papillae. A: Dorsal view; B: Lateral view; C: Ventral view. 268 Cybium 2014, 38(4)

Keith & Hadiaty Stiphodon anniaeae, a new species of goby from Indonesia Diagnosis The new species is a small Stiphodon with 14 pectoral rays, nine segmented rays in the second dorsal fin, 34-40 premaxillary teeth. No scales in the head and nape. The head and the jaw are long. The typical colouration of males is bright red, mottled with a blue pattern on the back. Description Scale counts in Stiphodon annieae n. sp. and related species are given in table II, number of premaxillary teeth in table I, and morphometrics in table III. Below, the holotype counts are given first followed in brackets, if different, by the paratype counts. Dorsal fins VI-I,9; D1 separate from and higher than D2; spine 3 elongate. Anal fin I,10 and directly opposite to second dorsal fin. Pectoral fin is with 14 rays, uppermost rays extending beyond membrane but not appearing feathery or silky, lowermost 1 or 2 rays simple; fin oblong with posterior margin rounded. Caudal fin with 12-13 branched rays, posterior margin rounded. Pelvic disc always with 1 spine and 5 stout and heavily branched segmented rays. Fifth rays joined together in their entire length forming a strong adhesive Table I. - Premaxillary teeth in Stiphodon annieae n. sp. and related species. Premaxillary teeth 25 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 42 43 44 45 S. annieae 1 1 S. mele 1 1 1 1 1 1 S.rubromaculatus 1 2 2 1 1 S. birdsong 1 2 6 8 10 14 8 3 7 2 1 3 1 1 S. surrufus 1 1 1 1 2 1 Table II. - Scale counts in Stiphodon annieae n. sp. and related species. Lateral scales 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 29 30 31 32 33 34 35 36 S. mele 2 1 1 1 2 S. rubromaculatus 1 1 2 1 2 S. birdsong 1 2 6 3 7 5 8 6 5 4 2 4 2 2 2 2 1 1 1 S. surrufus 1 1 1 1 1 1 Transverse back 3 4 5 6 7 8 9 10 11 12 13 14 15 S. annieae 2 S. mele 1 1 3 2 1 S. rubromaculatus 2 4 1 S. birdsong 4 3 3 14 16 14 7 1 S. surrufus 2 2 2 1 Transverse forward 0 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 S. mele 3 2 1 1 S. rubromaculatus 2 2 1 2 S. birdsong 2 2 6 2 7 7 13 9 5 4 4 1 1 1 S. surrufus 1 1 3 2 Predorsal (M: male, F: female) 0 1 2 3 S. annieae M 2 S. mele M 5 S. mele F 1 1 S. rubromaculatus M 6 S. birdsong M 32 S. birdsong F 55 S. surrufus M 3 S. surrufus F 2 1 Cybium 2014, 38(4) 269

Stiphodon anniaeae, a new species of goby from Indonesia Keith & Hadiaty Table III. - Morphometric values for Stiphodon annieae n. sp. and related species expressed to the nearest whole percent of standard length. Predorsal length 33 34 35 36 37 38 39 40 S. annieae 1 1 S. mele 2 1 1 1 1 S. rubromaculatus 1 2 2 2 S. birdsong 2 7 20 23 13 2 S. surrufus 2 1 2 1 Preanal length 48 49 50 51 52 53 54 55 56 57 58 59 S. annieae 1 1 S. mele 1 4 1 1 S. rubromaculatus 1 2 2 2 S. birdsong 1 3 9 6 10 9 11 10 7 S. surrufus 1 2 2 1 Head length 18 19 20 21 22 23 24 25 26 S. mele 2 1 1 2 1 S. rubromaculatus 3 4 S. birdsong 5 25 22 11 5 S. surrufus 2 4 Jaw length 6 7 8 9 10 11 12 Caudal peduncle depth 7 8 9 10 11 12 S. annieae 1 1 S. annieae 1 1 S. mele 1 2 3 1 S. mele 1 3 3 S. rubromaculatus 1 2 4 S. rubromaculatus 1 1 5 S. birdsong 6 37 23 1 S. birdsong 3 36 33 2 S. surrufus 1 2 2 1 S. surrufus 1 4 1 Caudal peduncle length 10 11 12 13 14 15 16 17 18 19 20 21 22 23 S. mele 2 2 1 1 1 S. rubromaculatus 2 2 2 1 S. birdsong 1 5 12 25 15 10 2 S. surrufus 1 1 4 Body depth at second dorsal origin in males 9 10 11 12 13 14 S. annieae 2 S. mele 1 3 1 S. rubromaculatus 1 3 2 S. birdsong 20 11 1 S. surrufus 1 1 1 Second dorsal fin length (M: male, F: female) 26 27 28 29 30 31 32 33 34 35 36 37 38 39 40 41 S. annieae M 1 1 S. mele M 1 1 1 2 S. mele F 1 1 S. rubromaculatus M 1 1 1 1 1 1 S. birdsong M 1 3 5 8 6 4 2 1 1 S. birdsong F 2 9 9 9 5 1 S. surrufus M 1 1 1 S. surrufus F 1 1 1 270 Cybium 2014, 38(4)

Keith & Hadiaty Stiphodon anniaeae, a new species of goby from Indonesia Table III. Continued. Anal fin length (M: male, F: female) 27 28 29 30 31 32 33 34 35 36 37 38 39 40 S. annieae M 1 1 S. mele M 2 1 1 S. mele F 1 1 S. rubromaculatus M 2 2 1 1 S. birdsong M 1 6 8 7 6 4 S. birdsong F 1 1 4 12 12 5 1 S. surrufus M 1 2 S. surrufus F 1 1 1 Caudal fin length (M: male, F: female) 17 18 19 20 21 22 23 24 25 26 27 S. annieae M 1 1 S. mele M 1 1 2 S. mele F 2 S. rubromaculatus M 1 1 3 1 S. birdsong M 1 3 3 2 2 2 S. birdsong F 1 1 8 6 1 S. surrufus M 1 2 S. surrufus F 1 2 disc; disc adherent to belly between fifth rays only; between spines a strong fleshy frenum. Scales in lateral series 18(19), those on caudal peduncle and the flanks below D2 are ctenoid and they become cycloid below the first dorsal fin in males. Anteriormost scale along midline nearly below posterior part of D1 or anterior part of D2. Scales in transverse backward series 9. Scales in transverse forward series 6(7). Scales in zigzag series 9. No scales in predorsal midline in male. Head, breast, nape, belly and pectoral base are without scales. Premaxillary teeth 34-40, fine and tricuspid, tridentiform with central cup longer than lateral cups. Dentary symphyseal teeth in males 1-2, conical to caniniform, stronger and larger than other teeth. Cephalic sensory pore system A, B, C, D, F, H, K, L, N and O; pore D missing in one specimen, single when present; all others are paired (Fig. 2). Oculoscapular canal separated into anterior and posterior canals between pores H and K. Cutaneous sensory papillae developed over lateral surface of head and body. Urogenital papilla in males somewhat rectangular with a rounded distal tip. Colour in preservation Male. Background of body whitish to yellowish; scales along and above midline and below second dorsal fin yellowish; belly entirely blackish. Background of head, chin and preopercle brownish. Inferior part of head and isthmus entirely blackish to brownish. Top of head brownish. Pectoral fins hyaline with a black patch at their base. Occipital region with brownish pigment. Preopercle behind eye brownish. First and second dorsal fins whitish; anal and caudal fins whitish; pelvic disk whitish. Female. Unknown, but male and female of Stiphodon usually have different colour patterns (Watson et al., 2005; Keith et al., 2007; Maeda and Tan, 2013; Maeda, 2014). Colour in life (Fig. 1) Male. Bright red on body sides. Many blue spotted areas from different sizes on dorsal part of body, from below first dorsal fin to caudal one. Top of head greyish with many red spots. A blue to green line passes below the eye from snout to pectoral fin. Area below this line from chin and isthmus to pectoral and pelvic fin bases is black. Dorsal fins bright red with few black spots on rays. Second dorsal fin with a distal blue line. Caudal fin bright red with a half blue line along margin, and a second one in the uppermost part. Pectoral fins hyaline with a black patch at their base. Belly whitish. Female. Unknown. Comparison Stiphodon annieae n. sp. differs from S. mele, S. rubromaculatus, S. birdsong and S. surrufus in having no blackish stripes (aligned spots) on dorsal fins (or just few irregular spots) vs. having well marked regular blackish stripes (aligned spots), a longer head (25-26 vs. 18-23%SL) and jaw length (10-12 vs. 6-10%SL), and a different colour pattern in Cybium 2014, 38(4) 271

Stiphodon anniaeae, a new species of goby from Indonesia Keith & Hadiaty male. It differs also from S. rubromaculatus in having more premaxillary teeth (34-40 vs. 27-32), and from S. mele and S. surrufus in having shorter second dorsal (30-32 vs. 33-38/37-39%SL) and anal fins (30-32 vs. 37-40/38-40%SL) in males. Distribution Currently known only from Halmahera (Indonesia). Ecology Like other Sicydiinae, Stiphodon annieae n. sp. was found in a clear, high gradient stream with rocky bottom. It lives on the bottom of the river, on top of rocks. It is assumed to be amphidromous (Keith, 2003; Keith and Lord, 2011b). Etymology The new species is named for Annie, the first author s wife, in recognition of her patience and unfailing support during all field trips in Pacific Islands. Acknowledgments. We wish to thank Daisy Wowor and Sopian Sauri for their help during the field sampling in Halmahera, Gono Semiadi, the LIPI coordinator for the project, the Division Environment of Weda Bay Nickel, Gavin Lee, Eka and the staff. Part of the present study was funded by Weda Bay Nickel and the Indonesian Institute of Sciences (LIPI), the French Ichthyological Society (SFI) and the Fondation de France. Finally, we thank for the loan of specimens: S. Morrison (WAM); P. Pruvost, R. Causse, Z. Gabsi, C. Ferrara, and for X-rays, M. Hautecoeur (MNHN). REfErences Akihito Prince, 1986. - Some morphological characters considered to be important in gobiid phylogeny. In: Indo-Pacific Fish Biology: Proc. 2 nd Int. Conf. on Indo-Pacific Fishes, pp. 629-639. Tokyo: Ichthyological Society of Japan. BIRDSONG R.S., MURDY E.O. & PEZOLD F., 1988. - A study of the vertebral column and median fin osteology in gobioid fishes with comments on gobioid relationships. Bull. Mar. Sci., 42: 172-214. 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