BULLETIN OF MARINE SCIENCE, 66(2): 457–466, 2000 NEW SPECIES PAPER

CALLOGOBIUS NIGROMARGINATUS, A NEW SPECIES OF GOBY (PISCES: ) FROM TAIWAN

Jeng-Ping Chen and Kwang-Tsao Shao

ABSTRACT Callogobius nigromarginatus, was collected from muddy-sand bottom close to a reef flat in Taitung County, southeastern Taiwan. This species has 25–26 lateral scale rows, thus belonging to the group with fewer scale rows as proposed by Goren et al. (1991). Diagnostic characters of this species include: fewer predorsal scales (5), 7–8 transverse scale rows, with posterior oculoscapular pores, three preopercular pores, pelvic fraenum present, and distinctive color pattern (broad stripe on 2nd dorsal and anal fin in adult). A key to all eight species of this low-scale-row group is also presented.

The Callogobius Bleeker, 1874 is characterized by having a depressed head with cutaneous papillose ridges; rear nostrils tubular; body elongate; 25–75 scales in the lat- eral series; pelvic fin small, frenum weak to moderately developed or absent; D.VI-I, 7- 15; A.I 6-13; P. 15-19; 26 or 27 vertebrae; caudal fin lanceolate or rounded. Callogobius has many junior synonyms. Koumans (1953) treated the following four genera as its junior synonyms: Ulcigobius Fowler, 1918, Metagobius Whitley, 1930, Crossogobius Koumans, 1931, and Batracheleotris Fowler, 1938. Mckinney and Lachner (1978a) excluded five nominal species which were originally described in Callogobius and listed 31 nominal species. However, 23 of the 31 species had been included variously in 10 other genera, e.g., Doryptena Snyder, 1908, Macgregorella Seale, 1910, Mucogobius McCulloch, 1912, Gunnamatta Whitley, 1928 and Intonsagobius Herre, 1943, are now treated as junior synonyms of Callogobius; the genus Galera Herre, 1927, preoccupied by Gray in Mammalia, and replaced by Herrea Whitley, 1930 is also a synonym of Callogobius (Eschmeyer, 1990); some other species were mistakenly assigned into the following four valid genera: Jordan and Seale, 1905, Eleotris Bloch and Schneider, 1801, Gobimorphus Gill, 1863, and Gobius Linnaeus, 1758. After Mckinney and Lachner (1978a) listed 31 Callogobius species, few researchers have dealt with Callogobius. Mckinney and Lachner (1978b) published a new species of C. stellatus. Goren (1978, 1979, 1980) added three species into this genus, namely C. clarki, C. bauchotae, and C. dori. Mckinney and Lachner (1984) described another new species of C. crassus and synonymized five species with C. maculipinnis (Fowler, 1918); combining C. trifasciatus Menon and Chatterjee, 1974, with C. flavobrunneus (Smith, 1958); and C. tutuilae (Jordan and Seale, 1906) with C. sclateri (Steindachner, 1879). The latest new species of this genus, C. amikami was described by Goren et al. (1991) from the Red Sea. In total, before this paper, Callogobius had 30 species in the world. Mckinney and Lachner (1984) pointed out that the following seven species of C. bauchotae, C. centrolepis Weber, 1909, C. crassus, C. flavobrunneus, C. maculipinnis, C. plumatus (Smith, 1959), and C. sclateri appear to form a discrete group within Callogobius, in having a stout-body shape, ctenoid scales, and a reduced number of segmented dorsal fin elements. Goren et al. (1991) also proposed another low-scale-row group (less than 26 rows along the body) with seven species in this genus. There are five species in common between these two groups. Goren et al. (1991) added C. dori and C. amikami into the low-

457 458 BULLETIN OF MARINE SCIENCE, VOL. 66, NO. 2, 2000 scale-row group and deleted C. sclateri and C. flavobrunneus from the stout-body shape group as defined by Mckinney and Lachner (1984). In Taiwan, four species of Callogobius were listed in Chen and Yu (1986), including C. liolepis Koumans, 1931, C. sclateri, C. snelliusi Koumans, 1953, and C. hasseltii (Bleeker, 1851). According to Mckinney and Lachner (1978a, 1984), C. liolepis should be removed from the genus Callogobius; and C. snelliusi is a junior synonym of C. maculipinnis. In book “ of Taiwan”, edited by Shen (1993), Lee (1993) revised gobiid fishes and excluded C. hasseltii from the Taiwanese fauna without further explanation. Shao and Chen (1993) added C. okinawae (Snyder, 1908) and Chen et al. (1996) added C. tanegasimae (Snyder, 1908). On 25 January 1994, two specimens of Callogobius were found and collected by the first author (JPC) in a rocky hole from Chengkung, Taitung County, southeastern Taiwan, located on the boundary between reef flat and sand bottom at about 10 m depth. On 9 March 1994, JPC collected another four specimens at Keehuei, a small local village near Chengkung. This undescribed species belongs to the low-scale- row Callogobius group, but differs from other Callogobius species by having the follow- ing characters: different pattern of cutaneous papilose, different number cephalic sensory pores, fewer predorsal scales, first dorsal shape, and distinct color pattern on vertical fins. The key to all 8 low-scale-row Callogobius is also provided.

MATERIALS AND METHODS

All specimens were collected from the southeastern coast of Taiwan by scuba diving during our survey of marine fish fauna in Taiwan. Fresh specimens were first photographed and the color pattern described. The fish were then fixed in 10% formalin and transferred to 70% enthanol. All counts and measurements were made from preserved specimens. Both meristic counts and morphormetric measurements are listed in Table 1. Methods of measurements and counts follow Hubbs and Lagler (1958), except counts of the longitudinal and transverse scale rows which follow Hoese and Obika (1988). The longtitudinal scale rows are counted from the upper pectoral origin to the base of the caudal fin, and the transverse scale rows are counted from the anal fin origin upward and backward to the 2nd dorsal fin. The terminology of the cephalic sensory system followed Miller (1986) and Wongrat and Miller (1991) which are based on Sanzo (1911). Vertebrae were counted from radiographs. Abbreviations used for these characters include: D, dorsal fin; A, anal fin; P1, pectoral fin; P2, pelvic fin; LR, longitudinal scale rows; TR, transverse scale rows; Pred.S, predorsal scales; SL, standard length; HL, head length; BD, body depth; Pred L, predorsal length;

SD2L, length of snout to 2nd dorsal origin; SAL, length of snout to anal origin; CPD, caudal pe- duncle depth; ED, eye diameter; SnL, snout length; HW, head width; and Int, interorbital width. In the following descriptions, data in parentheses refer to the paratypes, if it is different from the holotype. The type specimens are deposited at the Museum of Institute of Zoology, Academia Sinica, Taipei, Taiwan (ASIZP), and Bernice P. Bishop Museum, Honolulu (BPBM). Institutional abbre- viations forrow Leviton et al. (1985).

KEY TO THE SPECIES OF CALLOGOBIUS WITH LESS THAN 26 SCALE ROWS

1a. D VI-I,10; AI, 8 ...... C. amikami 1b. D VI-I, 7–9; AI, 6–7...... 2 2a. Pelvic frenum present ...... 4 2b. Pelvic frenum absent ...... 3 JENG-PING AND SHAO: NEW SPECIES OF CALLOGOBIUS 459

3a. D.VI-I, 9; Pred.S. 6; 1st dorsal fin higher than 2nd, 1st spine longest...... C. bauchotae 3b. D.VI-I, 7-8; Pred. S. 9–13; 1st dorsal fin not higher than 2nd, 3rd spine longest ...... C. crassus 4a. Pred.S. 7 or fewer; temporal sensory canal present ...... 5 4b. Pred.S. 9 or more; temporal sensory canal absent ...... 6 5a. Pred.S. 5; 3rd dorsal spine the longest ...... C. nigromarginatus 5b. Pred.S. 6-7; 1st dorsal spine the longest ...... C. maculipinnis 6a. Dark bands on body present ...... C. plumatus 6b. Dark dark bands on body absent...... 7 7a. D.VI-I, 7; caudal fin shorter than head length ...... C. centrolepis 7b. D.VI-I, 9; caudal fin longer than head length ...... C. dori

Figure 1. Callogobius nigromarginatus new species, holotype, ASIZP057695, male, 31.7 mm.

Callogobius nigromarginatus new species (Figs. 1,2)

HOLOTYPE.—ASIZP 057693, 31.7 mm SL, male, coastal waters off Keehui, Taitung County, southeastern Taiwan; muddy and sandy bottom of subtidal reef flats, 4 m, rotenone and hand net, J.P. Chen, 9 Mar. 1994. PARATYPES.—ASIZP 057694, 2 specimens 17.8 and 23.9 mm SL, and BPBM 37304, 23.9 mm SL, collected with holotype. ASIZP 057695, two specimens 19.5 and 27.4 mm SL, Chengkung, Taitung County, southeastern Taiwan, collected from muddy and sandy bottom similar to that of type locality of holotype, 10 m, J.P. Chen, 25 Jan. 1994.

Diagnosis.—This species is distinguished from other Callogobius species in having the following combination of characters: 5 predorsal scales; temporal sensory canal and pores present; preopercular canal with 3 pores; and 4 rows of sensory papillae with 3 transverse rows. D VI-I, 9, third spine longest; A I,7, posteriormost rays longest. Second dorsal and anal fin with a broad brown stripe in adult. Caudal fin rounded, slightly shorter than head length. Description.—Measurement and counts for the holotype and four paratypes are given in Table 1. D. VI-I, 9; A I-8; P1 17; P2 I,5; LR 26 (25–26); TR 7 (8); Pred. S 5; Vertebrae 11+15; pterygiophore formula 3(22110) branched caudal fin elements 8+7 = 15, seg- mented caudal-fin rays 17. Gill rakers 0+1+7. Body elongate in SL, laterally compressed, BD 4.0 (4.4–5.1); head depressed, HL 2.9 (2.7–3.0) in SL. Eye moderate, ED 4.3 (3.8–4.5); snout wider than ED, SnL 3.4 (3.2–4.2); 460 BULLETIN OF MARINE SCIENCE, VOL. 66, NO. 2, 2000

Figure 2. Cephalic sensory systems of the holotype of Callogobius nigromarginatus. Bar = 1 mm. JENG-PING AND SHAO: NEW SPECIES OF CALLOGOBIUS 461

Table 1. Morphometric data and meristic counts for Callogobius nigromarginatus. Measurement presented as percentages of standard length. Standard length is given in millimeters.

Ceharacters Heolotyp Paratyp A5SIZP057693 A4SIZP05769 ASIZP05769 Meristic Counts DIorsal fin rays V −II, 9 V −II, 9 V −II, 9 V −II, 9 V −I, 9 A7nal fin rays I7, I7, I7, I7, I, P7ectoral fin rays 171717171 L6ateral-line scales 252526262 T78888ransverse scales P55555redorsal scales V1ertebrate 1 +115 1 +115 1 +115 1 +115 1 +15 G--0ill raker +1+7- - Seex meal feemal meal feemal femal Morphometric measuarements S7tandard length 351. 149. 287. 197. 23. H5ead length 07.3 05.3 05.3 04.3 0.3 B5ody depth 03.2 02.2 00.2 02.2 0.2 S7nout to origin of dorsal fin base 01.3 07.4 01.3 07.4 0.3 S9nout to end of dorsal fin base 02.7 02.8 00.8 01.8 0.8 S3nout to origin of anal fin base 06.6 00.6 04.6 02.6 0.6 S0nout to end of anal fin base 04.8 02.8 01.8 00.8 0.8 S5nout to pectoral insertion 09.3 03.3 09.3 04.3 0.3 S2nout to pelvic insertion 04.3 00.3 06.3 04.3 0.3 S7nout to vent 08.5 07.5 07.5 03.5 0.5 L1ongest dorsal spine 09.2 00.1 07.2 09.1 0.1 L5ongest dorsal ray 08.2 09.1 07.1 09.1 0.1 L5ongest anal ray 04.2 04.2 08.2 01.1 0.2 P2ectoral fin length 08.3 08.2 04.2 00.3 0.3 P4elvic fin length 07.2 02.2 07.2 04.2 0.2 S0nout length 09.1 09.0 00.0 00.1 0.1 O8rbital diameter 09.0 08.0 09.0 09.0 0.0 U7pper jaw length 07.0 08.0 08.0 08.0 0.0 I3nterorbital space 04.0 02.0 03.0 03.0 0.0 C5audal peduncle depth 06.1 06.1 04.1 05.1 0.1 C2audal fin length 04.3 09.3 00.2 03.3 0.3

interorbital narrow, Int 13.3 (10.5–14.6) all in HL. Mouth small and oblique, lower jaw slightly protruding; maxilla reaching to vertical below posterior nostril; upper jaw length 4.9 (4.2–5.3) in HL. Anterior and posterior nostrils open at end of short tubes whose bases are located close to each other. Teeth in upper jaw consisting of two or three rows of pointed teeth; lower jaw with several rows anteriorly and tapering to two rows at end of jaw. Teeth of outer row of anterior part of lower jaw slightly enlarged. Tongue rounded. First dorsal fin is shorter than body depth and seperate from the 2nd dorsal fin, middle rays longest, 4.7 (4.9–5.8) in SL. Second dorsal fin slightly higher than 1st, longest ray (the last) 4.1 (5.2–5.7) in SL. Origin of 2nd dorsal fin slightly anterior to vertical through anus. Anal fin almost as high as 2nd dorsal fin, posteriormost rays longest 4.0 (4.1–5.4) in SL. Pectoral fin extending to vertical of base between 3rd and 4th anal rays, with length 462 BULLETIN OF MARINE SCIENCE, VOL. 66, NO. 2, 2000

of 3.1 (2.9–3.6) in SL. Pelvic short, 4.2 (3.6–4.6) in SL, reaching anus. Caudal fin 3.1 (2.9–3.5) rounded and shorter than HL; peduncle depth about half of length, 6.5 (6.1–7.0) in SL. SCALES.—Scales on body posteriorly to a vertical from 2nd or 3rd dorsal spine are ctenoid. Ctenoid scales on posterior body with 19–23 ctenii and arrayed in a single row along posterior margin. Scales on breast, belly, and anterior part of body cycloid. CANALS (see Fig. 1).—Nasal extension of anterior oculoscapular canal present, with pair of terminal σ pores slightly after posterior nostril. Anterior interorbital sections of oculoscapular canal united, with a single λ pore. A single κ pore in posterior interorbit. Pore ω present at posterodorsal edge of eye. Postorbital anterior oculoscapular canal with α, β pores and terminal ρ pore; and posterior oculoscapular canal present (terminal pores q and t). Preopercular canal present with three terminal pores, γ, δ and ε. SENSORY PAPILLAE.—All papillae of head present on edge of dermal fold except partial row i. Four main transverse rows 1, 2, 3 and 4 on cheek. Row 4 with 3 sections: oblique line 4s1 and straight line which is interrupted by row b into 4s2 and 4i. Row d along the ventral side of cheek toward the end of row 4i. Opercle with rows os, oi, and ot. Row x divided into 3 secions: x1, x2, and x3. Row z downward beyond the pore γ. Row e on the longest continuous dermal fold ranging from below the jaws and cheek and turning to- ward pore ε. Row i with anterior 3 transverse rows and the remaining part in a longitudi- nal arrangment. Row f paired and longitudinal. COLOR WHEN FRESH (holotype, Fig. 2).—Body light gray with of two dark gray irregular patches. First patch below first dorsal fin extending to pectoral-fin base, not extending to lower part of trunk. Second patch broad, as wide as second dorsal-fin base, extending to lower part of trunk and not connected with anal fin base, mottled with light spots and pale areas. Head pale, black spot extending from front of eye to posterior part of jaw. Sensory papillae on cheek darker than background. Nape areas with dark saddle. First dorsal fin gray with 3 light oblique bars, weakly joined, forming irregular color pattern. Second dorsal fin pale gray with broad black stripe centrally, with line of scattered light spots, and paralleled above by pale stripe. Anal fin with dark gray stripe, becoming wider in posterior membrane. Caudal fin black with many light spots forming irregular pattern; basal part of fin with broad irregular light bar. Pectoral fin dark gray with numerous light spots forming irregular lines. Pelvic fin gray, uniform. Color after preservation: Body pale yellow with brown patches and saddles. Light spots on body same color as background. Membrane of second dorsal and anal fin light gray at base, stripe dark brown. Color of caudal fin also changed to brown, pale basal part grey. Etymology.—This species is named for its blackish stripe at the outer margin of anal, and caudal fins. Distribution.—This new species has only been found at its type locality: Taitung County, southeastern Taiwan. Comparison.—C. nigromarginatus belongs to the low-scale-row Callogobius group (with 26 or fewer L.l.) as proposed by Goren et al. (1991). This species can be distin- guished from other species of this group by the following characters (listed in Table 2): five predorsal and 7–8 transverse scales, pelvic frenum present, and with posterior oculoscapular pores. C. nigromarginatus and C. maculipinnis are the only two species of this group that have posterior oculoscapular pores (temporal sensory pore). C. nigromarginatus is mostly close to C. maculipinnis but can be distinguished by fewer predorsal scales (4–5 vs 6–7), fewer transverse scales rows (7–8 vs 10), and the longest JENG-PING AND SHAO: NEW SPECIES OF CALLOGOBIUS 463

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ACKNOWLEDGMENTS

During the past five years (1989–1994), an intensive survey on inshore fish fauna in the waters around Taiwan was supported by a grant from the National Science Council of the Rebublic of China to the junior author (KTS). Also we thank M. Goren and S. C. Shen for reviewing and commenting on the manuscript.

LITERATURE CITED

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DATE SUBMITTED: August 9, 1999. DATE ACCEPTED: January 4, 2000.

ADDRESS: Laboratory of Fish Ecology & Evolution, Institute of Zoology, Academia Sinica, Nankang, Taipei 115, Taiwan, Republic of China. CORRESPONDING AUTHOR: (K.T.S.) Tel: +886-2-27899645; Fax: +886-2-27883463; Email .