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Research Article
Opistognathus ctenion (Perciformes, Opistognathidae): a new jawfish from southern Japan
expand article infoKyoji Fujiwara, Hiroyuki Motomura§, Gento Shinohara
‡ National Museum of Nature and Science, Tsukuba, Japan
§ The Kagoshima University Museum, Kagoshima, Japan
Open Access

Abstract

Opistognathus ctenion sp. nov. (Perciformes: Opistognathidae) is described on the basis of three specimens (17.3–30.6 mm in standard length) collected from the Osumi and Ryukyu islands, southern Japan in depths of 35–57 m. Although most similar to Opistognathus triops, recently described from Tonga and Vanuatu, the new species differs in mandibular pore arrangement, dorsal- and caudal-fin coloration, fewer gill rakers, and lacks blotches or stripes on the snout, suborbital region and both jaws.

Key words

Actinopterygii, dredge, new species, Osumi Islands, Ryukyu Islands, taxonomy

Introduction

Opistognathus Cuvier, 1816 is the most speciose genus of jawfishes (Perciformes: Opistognathidae), being distributed worldwide in tropical and temperate regions, except for the eastern Atlantic Ocean and Mediterranean Sea (Smith-Vaniz 2023); most species of Opistognathus occur in the Indo-West Pacific. A recent review of the genus by Smith-Vaniz (2023) recognized 60 valid species, 18 being new, and additional new species of Opistognathus were predicted. To date, valid species of Opistognathus total 91 overall (Smith-Vaniz 2023).

Examination of specimens in the Kagoshima University Museum, Japan (KAUM) and the National Museum of Nature and Science, Japan (NSMT) revealed an unidentified species of Opistognathus, collected in 35–57 m depth off the Osumi and Ryukyu islands, southern Japan. In common with the majority of species of Opistognathus, the number of known examples of the present species is small, due to difficulties in collecting, attributed to their small body size and cryptic habitat [for details see Smith-Vaniz (2023)]. Notwithstanding, the species is clearly distinct, having a unique combination of meristic characters and fresh coloration, and is here formally described as a new to science.

Material and methods

Morphological observation

Counts and measurements followed Smith-Vaniz (2023). Standard length (SL) was measured to the nearest 0.1 mm. Other measurements were made to the nearest 0.01 mm using needle-point calipers under a dissecting microscope (ZEISS Stemi DV4). Counts of vertebrae and fin rays, plus dorsal- and anal-fin pterygiophores, were examined from radiographs. Further osteological characters were investigated by computed tomography (CT) scanning using inspeXio SMX-225CR FPD HR Plus (Shimadzu, Kyoto) at 100 kV and 120 μA at a resolution of 18 μm, and three-dimensional reconstruction images produced by the rendering software VGSTUDIO MAX ver. 3.3 (Volume Graphics, Nagoya).

Preparation of figures

Photographs of preserved specimens were taken with a Nikon D850 camera using an internal focus bracketing function; sets of multifocal images were then collated into a composite image, using Adobe Photoshop. The distribution map was prepared using GMT ver. 5.3.1, with data from GSHHG (Wessel and Smith 1996). The names and grouping of islands in southern Japan (belonging to Kagoshima and Okinawa prefectures) follow Motomura and Matsunuma (2022: fig. 5.2).

Comparative data

Morphological characters of comparative species of Opistognathus are cited from Smith-Vaniz (2023).

Results and discussion

Opistognathus ctenion sp. nov.

Figs 1, 2, 3, 4, 5, 6; Table 1 New English name: Japanese Whitespotted Jawfish New standard Japanese name: Shiratama-agoamadai

Type material

Holotype. KAUM–I. 174226, 30.6 mm SL, off Mage-shima Island, Osumi Islands, Kagoshima, Japan, 35 m depth, dredge, 29 Sept. 2022, K. Kubota. Paratypes. KAUM–I. 174227, 26.2 mm SL, collected with holotype; NSMT-P 130174, 17.3 mm SL, southwest of Nagannu Island, Kerama Islands, southern Ryukyu Islands, Okinawa, Japan (26°14′33"N, 127°31′19"E26°14′30"N, 127°31′24"E), 53–57 m depth, dredge operated by R/V Toyoshio-maru (Hiroshima University), 19 May 2017, G. Shinohara.

Diagnosis

A species of Opistognathus distinguished from congeners by the following combination of characters: posterior end of upper jaw rigid, without flexible lamina; dorsal-fin rays XI, 16–18; anterior dorsal-fin spines very stout and straight, and their distal ends not transversely forked; anal-fin rays II, 17; gill rakers 6 or 7 + 13 or 14 = 20 or 21; vertebrae 10 + 22 = 32; longitudinal scale rows c. 40–50; lateral line terminating below 4th–6th soft ray of dorsal fin; 4th and 5th mandibular pore positions usually included 2 and 6–7 pores, respectively; body scales absent anterior to vertical below 4th or 5th dorsal-fin spine; vomerine teeth 2; body reddish-brown with 3 or 4 longitudinal rows of c. 8–10 whitish blotches; cheek and opercle with five or six whitish blotches; snout, suborbital region, and both jaws without blotches or stripes; spinous dorsal fin with ocellus between 2nd to 5th spines; dorsal-fin soft-rayed portion with two reddish-orange stripes; pectoral-fin base with one or two whitish blotches; caudal fin uniformly faint orange or reddish-yellow.

Description

General appearance of type specimens as in Figs 1, 2 and 3. Lateral line system and osteological features of the holotype are given in Figs 4 and 5, respectively. Lateral line system and scale descriptions based on KAUM–I. 174226, 174227 (not available for NSMT-P 130174 due to poor specimen condition). Counts and measurements of type specimens are given in Table 1.

Table 1.

Counts and measurements of Opistognathus ctenion.

Holotype Paratype Paratype
KAUM–I. 174226 KAUM–I. 174227 NSMT-P 130174
Standard length (mm; SL) 30.6 26.2 17.3
Counts
Dorsal-fin rays XI, 16 XI, 18 XI, 18
Anal-fin rays II, 17 II, 17 II, 17
Total pectoral-fin rays 19 (left) / 19 (right) 19 / 19 19 / –
Pelvic-fin rays I, 5 I, 5 I, 5
Procurrent caudal-fin rays 5 + 5 5 + 5
Branched caudal-fin rays 12
Segmented caudal-fin rays 8 + 8 = 16 8 + 8 = 16 8 + 8 = 16
Longitudinal scale rows c. 40–50 c. 40–50
Vertebrae 10 + 22 = 32 10 + 22 = 32 10 + 22 = 32
Gill rakers 7 + 13 / 7 + 14 = 20 / 21 6 + 14 / 6 + 14 = 20 / 20 – / 7 + 14 = 21
Measurements (% SL)
Pre-dorsal-fin length 32.3 32.5 35.1
Pre-anal-fin length 63.3 59.7 65.1
Dorsal-fin base length 62.9 63.5 59.8
Anal-fin base length 34.3 37.0 34.2
Pelvic-fin length 22.6 21.1 21.7
Caudal-fin length 20.9 23.2 22.2
Body depth 15.3 16.0 10.3
Caudal-peduncle depth 7.9 8.0 6.5
Head length 32.3 31.9 34.3
Postorbital length 19.8 20.5 19.1
Upper-jaw length 17.4 17.2 17.4
Postorbital-jaw length 6.8 5.5 4.3
Orbit diameter 10.0 10.5 11.2
As % of head length
Postorbital length 61.3 64.2 55.6
Upper-jaw length 53.9 53.8 50.8
Postorbital-jaw length 21.2 17.3 12.5
Orbit diameter 30.9 32.8 32.7
Figure 1. 

Holotype of Opistognathus ctenion (KAUM–I. 174226, 30.6 mm SL, off Mage-shima island, Osumi Islands, Kagoshima, Japan) A fresh and B preserved specimens photographed by KAUM and K. Fujiwara, respectively C X-ray image, photographed by K. Fujiwara.

Figure 2. 

Fresh coloration of two paratypes (A, C KAUM–I. 174226, 30.6 mm SL B, D KAUM–I. 174227, 26.2 mm SL) of Opistognathus ctenion, photographed by KAUM A, B lateral views C, D dorsal views.

Figure 3. 

Small paratype of Opistognathus ctenion (NSMT-P 130174, 17.3 mm SL) A fresh and B preserved specimens, photographed by G. Shinohara and K. Fujiwara, respectively.

Figure 4. 

Head of holotype of Opistognathus ctenion (KAUM–I. 174226, 30.6 mm SL), showing cephalic sensory pores (left column cyanine blue stain; right column solid yellow). Photographed by K. Fujiwara.

Figure 5. 

Three-dimensional reconstruction of head and anterior body in Opistognathus ctenion (KAUM–I. 174226, 30.6 mm SL), based on CT scanning. Photographed by G. Shinohara and K. Fujiwara. Abbreviations: ACh, anterior ceratohyal; Ana, anguloarticular; Bh, basihyal; Br, branchiostegal rays; Bsph, basisphenoid; Cl, cleithrum; Cor, coracoid; De, dentary; DHh, dorsal hypohyal; DPcl, dorsal postcleithrum; Ect, ectopterygoid; Ent, entopterygoid; Epoc, epiotic; Exoc, exoccipital; Fr, frontal; Hy, hyomandibular; Ih, interhyal, IO1 to IO5, 1st to 5th infraorbitals, respectively; Iop, interopercle; LE, lateral ethmoid; Met, metapterygoid; Mx, maxilla; Na, nasal; Op, opercle; Pa, parietal; Pal, palatine; PecR, pectoral radial; Pmx, premaxilla; Pop, preopercle; Psph, parasphenoid; Pt, posttemporal; Pte, pterotic; Q, quadrate; Ra, retroarticular; Sc, scapula; Scl, supracleithrum; Smx, supramaxilla; Soc, supraoccipital; Sop, subopercle; Sph, sphenotic; Ste, supratemporal; Sym, symplectic; Ur, urohyal; V1, 1st vertebral centrum; Vo, vomer; and VPcl, ventral postcleithrum. Asterisks indicate poorly resolved features.

Head and body. Body elongate, compressed anteriorly, progressively more compressed posteriorly. Anus situated just before anal-fin origin. Head cylindrical, its profile rounded. Eyes somewhat large, located dorsolaterally. Anterior nostril a short membranous tube with a tiny tentacle on posterior rim, when depressed not reaching posterior nostril; situated about mid-way between posterior nostril and dorsal margin of upper lip. Posterior nostril opening elliptical. Mouth terminal, obliquely inclined anterodorsally, forming angle of c. 20° with body axis. Anterior tip of upper jaw slightly before vertical through lower-jaw tip. Posterior margins of preopercle and opercle indistinct, covered with skin and generally rounded with slightly elongated flap on upper part, respectively. Gill opening wide, its uppermost point slightly below horizontal through dorsal margin of orbit in lateral view.

Lateral line system. Cephalic sensory pores moderately developed, covering most of head except for lower part of cheek and area adjacent to dorsal-fin origin. Mandibular pore positions 1 and 2 each with a single similarly-sized pore; position 3 with a single pore (largest size of mandibular pores); positions 4 and 5 with 1 (only left side of KAUM–I. 174227) or 2 and 6 or 7 pores, respectively. Lateral-line pores moderate, mostly in single series above and below embedded lateral-line tubes. Lateral line ending below 4th (KAUM–I. 174226) or 6th (KAUM–I. 174226) soft rays of dorsal-fin rays.

Scales. Scales mostly missing, scaled area and scale counts estimated from scale pockets. Lateral surface of body and belly scaled, except above and slightly below lateral line, area anterior to vertical below 4th (KAUM–I. 174227) or 5th (KAUM–I. 174226) dorsal-fin spine, pectoral-fin base, and chest. Head region and bases of vertical fins completely naked.

Fins. Dorsal fin moderately low, its profile relatively uniform except for anterior part and slightly notched junction of spinous and segmented rays; 1st dorsal-fin spine distinctly short, its base located between uppermost point of gill opening and posteriormost tip of flap on opercle; all dorsal rays branched distally. Anal fin of similar height to dorsal fin, its origin vertically level with base of 1st (KAUM–I. 174226) or 2nd (KAUM–I. 174227, NSMT-P 130174) dorsal-fin soft ray; last anal-fin ray close to caudal-fin base and vertically level with last dorsal-fin ray; all fin rays branched distally. Pelvic-fin origin anterior to vertical through dorsal-fin origin; first ray of pelvic fin robust, not tightly bound to second ray; membrane between first and second rays incised distally; second ray longest, innermost 3 rays branched. Pectoral-fin base below 2nd and 3rd dorsal-fin spine bases. Caudal fin rounded posteriorly.

Osteological features. Nasal short, tube-like. Vomer rhombic, with two tiny conical teeth anteriorly. Lateral ethmoid somewhat broad, articulating with 1st infraorbital and palatine ventrally. Palatine robust anteriorly, tapering posteriorly, without teeth. Infraorbitals relatively slender, comprising 5 elements, including dermosphenotic; 1st infraorbital longest, 3rd with suborbital shelf, 5th (= dermosphenotic) firmly attached to sphenotic. Basisphenoid crescentic. Frontal tapering anteriorly, 6 large dorsal openings for sensory canal from anteriormost tip to lateral aspect. Left and right parietals separated by supraoccipital. Anterior and posterior tips of supraoccipital strongly pointed. Sphenotic not expanded. Supratemporals associated with parietal and pterotic.

Premaxilla with a single row of conical teeth, except for posterior end. Maxilla long, posteriorly broadly expanded with slightly rounded corners. Supramaxilla small, on upper posterior end of maxilla. Dentary with a single row of conical teeth; 5 large ventral openings (including on posterior tip) from mandibular sensory canal. Anguloarticular large, its anterior projection fitting into dentary notch; coronoid process strongly pointed, directed anterodorsally. Retroarticular small, on ventroposterior corner of anguloarticular. Hyomandibular broadly attached to sphenotic and pterotic. Ectopterygoid and symplectic slender. Entopterygoid forming a large shelf. Metapterygoid and quadrate present but poorly resolved, Opercle with 2 strong and 1 weak ridge. Preopercle with 5 large openings from preopercular sensory canal. Subopercle small, its anterior tip pointed. Interopercle triangular, size similar to subopercle. Six long recurved branchiostegal rays.

Posttemporal L-shaped, forked, dorsal limb articulating with epiotic, an opening on posterior corner. Supracleithrum rod-like. Cleithrum with a large dorsal blade, receiving supracleithrum. Dorsal postcleithrum rectangular, articulating with cleithrum and scapula. Ventral postcleithrum long, narrow. Scapula widely separated from coracoid. Pectoral-fin radials comprising 4 elements, lowermost distinctly largest. Supraneural bone absent. Anterior dorsal- and anal fin interdigitation patterns //1/1+1/1/ and //1+1/1/1/1/, respectively.

Coloration

Fresh coloration of holotype and KAUM–I. 174227. Head ground color reddish-brown dorsally, reddish-white ventrally. Iris generally reddish-brown, except for whitish area ventrally, with four faint dark red lines radiating from pupil. Two faint dark-red oblique lines, extending from just behind eye to middle of nape and upper part of cheek, respectively. Five or six whitish blotches on cheek and opercle. Floor of mouth entirely white No blotches or stripes on snout, suborbital region, and both jaws. Body reddish-brown, with 3 or 4 longitudinal rows of c. 8–10 whitish blotches of size distinctly smaller than blotches on head region; upper one or two rows and anterior part of lower two rows of blotches somewhat indistinct. Two whitish blotches on pectoral-fin base, lower blotch distinctly the larger. Dorsal- and anal-fin bases edged with dark reddish-brown, anterior edge of former extending slightly below lateral line (sometimes interrupted by body ground color). Spinous dorsal fin greenish- or yellowish-brown; an ocellus between 2nd to 5th spines, 4–6 white spots forming a longitudinal row just behind ocellus. Soft-rayed part of dorsal fin and anal fin hyaline or faint reddish-brown, with two and one reddish-orange stripes, respectively; upper stripe of former through distal edge, remaining stripes at c. 1/3 height of both fins. Pelvic-fin rays whitish and membrane hyaline with melanophores. Pectoral and caudal fins uniformly faint orange or reddish-yellow.

Fresh coloration of NSMT-P 130174. Generally similar to other type specimens, with the following differences. Head and body yellow. Whitish blotches on body more distinct. A whitish blotch on pectoral-fin base. Vertical fins faintly yellow (details of pigmentation patterns not visible), an ocellus on spinous dorsal fin. Pelvic fins white.

Color in alcohol. Head and body generally blackish-gray. Ventral part of head and belly white. Whitish blotches on cheek, opercle, and pectoral-fin base (in fresh condition) faded, traces of blotches on body represented by non-pigmented areas. Spinous dorsal fin generally blackish-gray, an ocellus apparent (with hyaline white edge), but longitudinal row of white spots faded. Soft-rayed part of dorsal and anal fins hyaline, reddish-orange stripes (in fresh condition) retained as blackish-gray stripes. Pelvic-fin rays white, membrane hyaline with melanophores. Pectoral and caudal fins uniformly translucent white.

Distribution and habitat

Currently known only from the Osumi and Ryukyu islands, southern Japan in depths of 35–57 m (Fig. 6). The Ryukyu specimen (NSMT-P 130174) was collected from a sandy gravel bottom.

Figure 6. 

Distributional records of Opistognathus ctenion.

Etymology

The specific name is a noun in apposition derived from the Greek diminutive κτενίον, meaning “a small comb”. It refers to the low gill raker numbers in the new species, one of the lowest recorded for Indo-Pacific species of Opistognathus (see below).

Comparisons

Opistognathus ctenion keys out to couplet 25 in Smith-Vaniz’s (2023) key to species of Opistognathus (including all valid species known from the Indo-West Pacific to date). The new species is most similar to the allopatric Opistognathus triops Smith-Vaniz, 2023 in having the following characters: posterior end of upper jaw rigid, without flexible lamina; dorsal-fin rays XI, 16–18; anal-fin rays II, 17; vertebrae 10 + 22 = 32; longitudinal scale rows c. 40–50; body scales absent anterior to vertical below 4th or 5th dorsal-fin spine; vomerine teeth 2; lateral line terminating below 4th–6th soft ray of dorsal fin; and spinous dorsal fin with an ocellus between 2nd to 5th spines. However, O. ctenion differs distinctly from O. triops in having fewer gill rakers (6 or 7 + 13 or 14 = 20 or 21 in O. ctenion vs 8 or 9 + 16–18 = 24–27 in O. triops), usually 2 and 6 or 7 pores included in the 4th and 5th mandibular pore positions, respectively (vs 1 and 2–4 pores, respectively), two reddish-orange stripes on the soft-rayed part of the dorsal fin (vs three broken brown stripes), a uniformly faint orange or reddish-yellow caudal fin (vs hyaline with three brown bars), and no blotches or stripes on the snout, suborbital region, and both jaws (vs 4 or 5 brown lines radiating from orbit). In addition, O. ctenion apparently occupies a slightly deeper water habitat than O. triops (currently known from 35–57 m depth vs 12–32 m depth).

The total of 20 or 21 gill rakers in O. ctenion is one of the lowest among the Indo-Pacific species of Opistognathus, with only two species sharing similar counts [viz., Opistognathus albomaculatus Smith-Vaniz, 2023 with 19–22 gill rakers; and Opistognathus reticulatus (McKay, 1969) with 21–23; see Smith-Vaniz (2023: table 12)]. Although O. ctenion is unlikely to be misidentified as O. reticulatus due to significant differences in body color, it is somewhat similar to O. albomaculatus in sharing whitish blotches on the body. However, the former can be easily distinguished from O. albomaculatus by the ocellus on the spinous dorsal fin (vs a striped pattern in O. albomaculatus). Dorsal- and anal-fin ray, and caudal vertebral numbers, as well as vomerine teeth condition, are also useful for distinguishing between the two species (viz., XI, 16–18 and II, 17, respectively in O. ctenion vs X, 19–21 and II, 18–20 in O. albomaculatus; 22 vs 23–25; and two teeth present vs teeth absent).

Acknowledgments

We are especially grateful to K. Kubota (Kagoshima University), S. Ohtsuka and Y. Kondo (Hiroshima University), Captain K. Nakaguchi and the crew of the R/V Toyoshio-maru for their assistance in collecting the specimens of the new species; S. Nomura, T. Kutsuna and Y. Shigeta (NSMT) for their efforts on proper maintenance of micro-CT scanner and software in Research Wing, Tsukuba District; G. S. Hardy (Ngunguru, New Zealand) for reading the manuscript and providing help with English; W. Smith-Vaniz (Florida Museum of Natural History) for reading the manuscript and providing valuable comments.

Additional information

Conflict of interest

The authors have declared that no competing interests exist.

Ethical statement

No ethical statement was reported.

Funding

This study was supported in part by a Grant-in-Aid from the Japan Society for the Promotion of Science for JSPS Fellows to KF (PD: 22J01404); JSPS KAKENHI Grant Numbers 20H03311 and 21H03651, the JSPS Core-to-Core CREPSUM JPJSCCB20200009, and the “Establishment of Glocal Research and Education Network in the Amami Islands” project of Kagoshima University adopted by the Ministry of Education, Culture, Sports, Science and Technology, Japan to HM; and the Integrated Research Program “Geological, Biological, and Anthropological Histories in Relation to the Kuroshio Current” of the National Museum of Nature and Science, Tsukuba (2016–2021) and JSPS KAKENHI Grant Number JP21K01009 to GS.

Author contributions

K.F. was responsible for the study design, generation and analysis of the data, and wrote the original draft manuscript. H.M. and G.S. were responsible for field work, generation and analysis of data, and review and editing of the manuscript. All authors read the manuscript and approved the final version.

Author ORCIDs

Kyoji Fujiwara https://orcid.org/0000-0001-7577-8333

Hiroyuki Motomura https://orcid.org/0000-0002-7448-2482

Gento Shinohara https://orcid.org/0000-0002-8071-9239

Data availability

All of the data that support the findings of this study are available in the main text.

References

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  • Motomura H, Matsunuma M (2022) Fish diversity along the Kuroshio Current. In: Kai Y, Motomura H, Matsuura K (Eds) Fish diversity of Japan. Evolution, Zoogeography, and Conservation. Springer Nature Singapore Pte Ltd., Singapore, 63–78. https://doi.org/10.1007/978-981-16-7427-3_5
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