INTRODUCTION
An interesting goby was noted firstly from the Saekkiseom which has been known as a famous diving point of Korea located in the southern coastal waters of Jejudo Island, Korea by Choi et al. (2013) in their underwater survey results showing ichthyofauna with about 90 fishes observed around the island from 2009 to 2010. In their results, a goby was observed in front of a shelter on coarse sandy bottom, and a single underwater photograph of the goby was presented and featured by having separated pelvic fins and five dark reddish vertical bands from head to caudal peduncle on lateral body. They identified the goby as Amblyeleotris sp. A symbiosis goby genus Amblyeleotris Bleeker, 1874 is the most speciose genus comprising more than 36 species in the world (Jaafar and Randall, 2009). However, there was no report on the occurrence of Amblyeleotris species from the Korean waters to date, except for that of Choi et al.(2013).
The authors are conducting an underwater survey to understand characterisctics of the fishfauna in the southern coastal waters of Jejudo Island, especially around three islands comprising Beomseom, Munseom, and Seopseom islands since 2015. During the recent survey a single specimen belongs to the genus Amblyeleotris showing symbiotic association with a snapping shrimp, Alpheus sp. on the sandy bottom of the Seopseom Island was observed and collected by a plastic trap handmaded. The goby was subsequently identified as A. japonica Takagi, 1957 which represents the first record from Korea as well as the same species observed by Cho et al. (2013). We, therefore, describe the species for providing detailed morphological features to understand further symbiotic characteristics between the goby and a snapping shrimp as well as its biological information from Korea. Counts and measurements follow those of Hoese and Steene (1978), and specimen examined is depostited in the fish collection of the National Institute of Biological Resources, Korea (NIBR-P). The numbers of vertical fin rays and vertebrae were counted from radiograph (Softex CMB-2, Japan). The dorsal pterygiophore formula (DPF) and designation of the sensory canal pores follow those of Akihito et al.(1984).
TAXONOMIC ACCOUNTS
Genus Amblyeleotris Bleeker, 1874
(New Korean name: Se-u-but-i-mang-dug-sog)
Emblyeleotris Bleeker, 1874: 373 (type species: Eleotris periophtalmus Bleeker, 1853, by original designation and monotypy).
Cheek with transverse and longitudinal papillae rows; two longtitudinal rows, uppermost extends posteriorly from fifth or sixth transverse rows; mandibula papillae reduced to a single enlarged papilla on each side of chin, set in a depression; gill opening broad, extending from upper opercular attachment below to well before posterior margin of preoperculum; body scales ctenoid posteriorly, cycloid anteriorly; second dorsal and anal fin rays I, 12 to 20; head compressed, with eyes placed high on sides of head; interorbital much narrower than eye; head pores present, 2 median unpaired interorbital pores; pelvic fins connected or seperate (Hoese and Steene, 1978).
Remarks. The genus is the most speciose group among gobiid genera showing symbiotic association with shrimps and distributed widely in the Indo-West Pacific Ocean. From the northern West Pacific, totally 13 species have been recognized to date, i.e., all species from Japan (Akihito et al., 2013), seven species from Taiwan (Chen et al., 1998), a single species(A. japonica) from Korea at present (this study).
Amblyeleotris japonica Takagi, 1957
(New Korean name: Bulg-eun-dong-gal-se-u-but-i-mang-dug) (Figs. 1~2; Table 1)
Fig. 1. Fresh specimen (above) and its X-ray radiograp (below, reverse image) of Amblyeleotris japonica, NIBR-P0000080204, 70.5 mm SL, collected from southern Jejudo Island, Korea.
Fig. 2. Dorsolateral (A), lateral (B), and ventrolateral (C) aspects of head in Amblyeleotris japonica (NIBR-P0000080204, 70.5 mm SL). AN and PN, anterior and posterior nostrils, respectively; Bʹ to Hʹ, anterior oculoscapular canal pores; Kʹ to Lʹ, posterior oculoscapular canal pores; Mʹ to Oʹ, preopercular canal pores. Apostrophes, terminal pores of canals and S, single pore. The arrow shows an attachment position of gill membrane to isthmus and bar indicates 5 mm.
Amblyeleotris japonicus Takagi, 1957: 105, pl. 5 (figs. a~b), fig. 2 (type locality: tide pool at Kan-no-se, Kagoshima Bay, Kagoshima Pref., Japan); Hoese and Steene, 1978: 387 (Japan); Mohlmann and Randall, 2002: 219 (Japan); Wu et al., 2009: 66 (Taiwan); Kohda et al., 2017: 22, fig. 1 (Japan).
Amblyeleotris japonica: Akihito, 1984: 255, fig. 95, Pl. 242-C (Wakayama Pref., Ogasawara Islands to Ishigakijima, Japan); Suzuki and Senou, 1993: 602, photo (Chiba Pref., Tsushima to Kagoshima Pref., Japan); Chen et al., 1998: 113, figs. 4~5 (northern Taiwan and Penghu); Hayashi and Shiratori, 2003: 137 (south of Chiba Pref., Tsushima to Kagoshima Pref., Japan); Senou et al., 2004: 335, photos(Izu Islands, Chiba Pref. and Tsushima to Kagosima Pref., Japan); Motomura et al., 2010: 203, fig. 483 (Yudomari, Kagoshima Pref., Japan); Akihito et al., 2013: 1502 (Izu Islands, Chiba Pref., Hakoyama Bay to Yakushima Islands, Simane Pref., Nagasaki Pref., Japan); To and Shea, 2016: 11, fig. 2 (Hong Kong).
Amblyeleotris sp.: Choi et al., 2013: 49, fig. 2 (Jejudo Island, Korea).
Material examined. One specimen, NIBR-P0000080 204, 70.5 mm SL, 14 m depth, off Bomok-dong, Seogwipo-si, Jeju-do, Korea, 13 November 2021, B. J. Kim, S. K. Kim, and S. H. Lee, homemade trap.
Description. Comparison of meristic counts are provided in Table 1. Dorsal fin rays VI-I, 13; anal fin rays I, 14; pectoral fin rays 17, uppermost ray unbranched; pelvic fin rays I, 5, joined basally by a membrane, pelvic frenum present; longitudinal scale rows 84; transverse scale rows ca. 28; segmented caudal fin rays 9+8; branched caudal fin rays 7+7; predorsal scales absent; DPF, 3/II II I I / 0 / 9; vertebrae 26. Measurements in % SL: head length (HL) 24.4; predorsal length 29.8; prepelvic length 30.1; preanal length 53.5; basal length of first dorsal fin 20.4; basal length of second dorsal fin 35.3; basal length of anal fin 33.2; length of caudal peduncle 15.6; depth of caudal peduncle 10.9; length of pectoral fin 24.8; length of pelvic fin 27.1; length of caudal fin 38.7; body depth at anus 16.5; body width posterior to gill opening 10.5; first spine length of first dorsal fin (FDF) 22.8; second spine length of FDF 25.4; third spine length of FDF 26.3; fourth spine length of FDF 22.4; spine length of second dorsal fin 13.5; first ray length of second dorsal fin 13.0; spine length of anal fin 8.7; first ray length of anal fin 9.5; spine length of pelvic fin 8.5. Measurements in % HL: head width 65.7; head depth 52.9; snout length 23.3; orbital diameter 25.6; interortbital distance 5.8; upper jaw length 42.4.
Table 1. Comparison of diagnostic characters of Amblyeleotris japonica between the present study and previous works
Head and body elongate and moderately copresssed. Snout short and dorsal profile of head steep. Anterior nostril a short conical tube; posterior one simple tube touching margin of orbit. Eyes large, its upper lim projected dorsally and interorbital space narrow. Mouth large and oblique; its posterior edge extending to a vertical at center of pupil; lower jaw slightly projected; tongue rounded free from mouth floor. Gill opening extending forward to a vertical about one half orbit diameter behind eye.
Cephalic sensory system (Fig. 2). Anterior oculoscapular canal with Bʹ, C, D, E, F, G, and Hʹ. C and D singular, between interorbitals; posterior oculoscapular canal with Kʹ, and Lʹ, preopercular canal with Mʹ, N, and Oʹ, sensory papillae in a transverse pattern.
Color when fresh. Head and body pale beige with five pale brownish bands from posterior part of head to base of caudal fin. Antero-dorsal part of head, between tip of snout to eye, dusky. Among bands five dusky spots along dorsal midline, anterior three spots continued a thin line ventrally. Dorsal fin nearly transparent. Pectoral fin transparent without any dark marking. Pelvic fin dusky at inner rays. Anal fin with a thin dusky line and dusky marginally. Caudal fin transparent with a pale dusky C-shaped marking.
Color after preservation. Ground colors of head and body light beige. Pale brownish four veritcal bands from first dorsal fin to caudal peduncle on lateral body. Five dark spots on dorsal midline from origin of first dorsal fin to base of caudal fin; first spot on origin of first dorsal fin, second one on origin of second dorsal fin, third one on mid-portion of second dorsal fin, fourth one posteriormost base of second dorsal fin.
Ecological notes. Amblyeleotris japonica was firstly noticed at the depths of about 10~15 meters of Seopseom Island, Jeju-do, Korea on 28 May 2019 (pers. obs.). The species has been generally observed in the same locality of the island with one or two snapping shrimps belong to the genus Alpheus.
Distribution. Known from Indo-West Pacific: Taiwan (Chen et al., 1998; Wu et al., 2009), Hong Kong (To and Shea, 2016), Japan (Takagi, 1957; Suzuki and Senou, 1993; Hayashi and Shiratori, 2003; Motomura et al., 2010) and Korea (Choi et al., 2003; present study). In Korea, only from southern coastal waters of Jejudo Island, Korea at present.
Remarks. Thirty-eight species have been known as vaild in the genus Amblyeleotris, distributed in the Indo-Pacific (Froese and Pauly, 2023). Particularly, lots of species reported from the adjacent country of Korea, that is, 13 species were known from the Japanese waters(Akihito et al., 2002) and 11 species from the South China Sea (Chen et al., 1998). From Korea, however, only a single species of Amblyeleotris sp. was seem to be inhabited in the southern coastal waters of Jejudo Island (Choi et al., 2013), although its entity was unclear. In the present study, we were able to collect a single specimen belongs to Amblyeleotris from the sandy bottom at a depth of 14 m near rocky reef of the Seopseom Island, Jeju-do, Korea. It was characterized by having a prominent ventral frenum, a lower number of scales in longitudinal series, a rather compressed body, anterior limit of opercular opening located below between posterior margins of eye and preopercle, second dorsal fin with a single spine and 13 soft rays, and anal fin with a single spine and 14 soft rays, and five dusky vertical bands on lateral body from head to caudal peduncle when fresh. These morphological charcaters were well accordance with those of the previous reports as well as the diagnostics of the original description of A. japonica by Takagi (1957) as show in Table 1. We finally the specimen collected from the southern coastal waters of Jejudo Island, Korea in the present study identifed as A. japonica, representing the first record of the species from Korea.
A. japonica is most similar to A. rubrimarginata Mohlmann and Randall, 2002 in having simlar dorsal and anal fin ray counts as well as pelvic fin structure. The former species, however, can be easily differentiated from the latter by a lower number of longitudinal scale rows (69~78 vs. 81~86) and a dark spot behind eye (absence vs. presence) as mention by Mohlmann and Randall(2002).
It is Septermber 2019 that the first occurrence of A. japonica in the southern coastal waters of Jejudo Island, Korea. Since then, we can observing the species continously at the same locality of the island and several pairs of the species were also observed for five years. It is needed to conduct additional long-term study for clarify their symbiotic association with a Alpheus shrimp as well as its sound settlement in the areas of Jeju Island, Korea in the near future. New Korean names, “Se-u-but-i-mang-dug-sog”, and “Bulg-eun-dong-gal-se-u-but-i-mang-dug” are proposed for the generic and specific names of A. japonica, respectivly, derived from its unique symbiotic association with shrimps and its reddish color of vertical bands of lateral body.
ACKNOWLEDGEMENTS
This work was supported by a grant from the National Institute of Biological Resources, funded by the Ministry of Environment of the Republic of Korea (NIBR No. 202203106).
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