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Callogobius albipunctatus sp. nov. and Callogobius dorsomaculatus sp. nov. are described from Japan. Both species are included in the sclateri group, characterized by elongate ctenii on the caudal fin base scales, the female urogenital papilla with two lateral projections, and the presence of cephalic sensory papillae Row 20 (preopercular row). Callogobius albipunctatus is characterized by cephalic sensory papillae Row 16 (transverse mandibular rows) comprising 10 papillae rows and a posteriormost single papilla, connected pelvic fins with a low frenum and concave posterior margin, cephalic sensory canal pores B'D(s)FH', 25–29 longitudinal row scales, 8–10 transverse row scales, and 7–11 predorsal scales, and C. dorsomaculatus by Row 16 comprising 11 papillae rows and a posteriormost single papilla, connected pelvic fins with a concave posterior margin but lacking a frenum, cephalic sensory canal pores B'C(s)D(s)EFH' or B'C(s)D(s)EFGH', 20–26 longitudinal row scales, 7–9 transverse row scales, and 6–10 predorsal scales. The cephalic sensory system in juvenile C. albipunctatus is described. Row 16, which is represented by three patterns within the genus, is redefined.

Thrissina supra sp. nov. is described based on 15 specimens collected from Sindh, Pakistan. The new species is closely related to Thrissina whiteheadi (Wongratana 1983), which is herein redescribed, both species having a relatively long upper jaw with the posterior tip slightly beyond the opercle posterior margin, the snout tip above the eye center level, similar numbers of gill rakers, ventral scutes, and fin rays, and the first supramaxilla absent. However, the former is characterized by higher counts of longitudinal scale rows (45–47 vs. 40–42 in T. whiteheadi), transverse scales (12 or 13 vs. 10 or 11), total gill rakers on the first, second, third, and fourth gill arches [35–39, 33–37, 22–24, and 18–22, respectively vs. 30–34 (rarely 36), 29–32 (34), 19–21 (23), and 15–18 (14, 19), respectively], and branched anal-fin rays [42–45 (rarely 40) vs. 39–42 (43)], a longer snout (3.7–4.1% SL vs. 3.1–3.6%), pelvic fin (9.0–10.4% SL vs. 7.7–9.0%), and mandible (17.3–18.3% SL vs. 15.4–17.2%), a shorter pelvic-fin insertion to anal-fin origin distance (17.0–18.8% SL vs. 19.1–24.2%), and distinct paired dark lines along the dorsum from the occiput to the caudal-fin base (vs. uniformly distributed dorsal melanophores).

A new atherinid fish, Doboatherina palauensis, is described based on the holotype and 31 paratypes, 36–51 mm in standard length, collected from the marine lakes and outer lagoon in Mecherchar Island, Republic of Palau. The new species can be distinguished from all congeners by a short, blunt ascending process of the premaxilla (height about twice maximum width), premaxilla with a single lateral process, posterior upper margin of dentary with a small process, palatine toothed, no crenulation along posterior margin of lateral and predorsal scales, smaller eye (diameter 9.2–11% of standard length), 37–39 midlateral scales, 38–41 total vertebrae, narrower midlateral band (about 1/2 width of midlateral scale, its upper and lower margins not reaching to upper and lower margins of midlateral scale row at the level of anal-fin origin, respectively). The new species resembles Doboatherina aetholepis (Kimura, Iwatsuki and Yoshino 2002), Doboatherina bleekeri (Gunther 1861), Doboatherina valenciennei (Bleeker 1854) and Doboatherina woodwardi (Jordan and Starks 1901) in sharing a comparatively slender body in the genus Doboatherina. The former is distinguishable from D. aetholepis by having only a short spatular outgrowth on posterior margin of predorsal and/or interdorsal scales or almost lacking the outgrowth (vs. a long spatular outgrowth on posterior margin of most predorsal and interdorsal scales in D. aetholepis) and narrower midlateral band (lower margin not reaching to lower margin of midlateral scale row vs. reaching), from D. bleekeri and D. valenciennei by lacking crenulated lateral and predorsal scales (vs. having crenulated lateral and/or predorsal scales) and a single lateral process on premaxilla (vs. two processes), and from D. woodwardi by having lower ascending process (height about twice maximum width vs. three times) and a single lateral process on premaxilla (vs. two processes). Doboatherina bleekeri has more numerous total vertebrae (42–47) than D. palauensis (38–41).

A new species of goatfish, Parupeneus williamsi, is described on the basis of 12 specimens (43.9–234.3 mm in standard length) collected from the Marquesas Islands, French Polynesia. The species closely resembles Parupeneus multifasciatus (Quoy and Gaimard 1825) in sharing white to yellowish barbels, its tips usually extending beyond the posterior margin of the preopercle, two or three blackish vertical bands (including indistinct bands) on the trunk, and a blackish saddle on the upper caudal peduncle. However, the new species is distinguished from P. multifasciatus by having all of the bands and saddle very indistinct, dense melanophores uniformly distributed on the anal-fin membranes (preserved specimens), upper jaw slightly slender and shorter in specimens larger than 50 mm SL, and slightly longer second anal-fin soft ray. The morphological differences between the two species are supported by a previously published molecular analysis of mitochondrial cytochrome b sequences. Although P. multifasciatus is widely distributed in the eastern Indian and Pacific oceans, P. williamsi is endemic to the Marquesas Islands.

Thrissina belvedere sp. nov. is described from 14 specimens collected in Ha Long Bay, northern Vietnam. The new species is closely related to Thrissina chefuensis (Gunther 1874) (redescribed herein), both species having a short upper jaw with the posterior tip slightly shortened to the posterior margin of the preopercle, an indistinct black blotch on the nape (but not on the dorsum just before the dorsal-fin origin), and similar numbers of scutes on the ventral edge of the body. However, the former is characterized by higher total gill-raker counts on the first, second, third, and fourth gill arches, and the third gill arch posterior face (59–66, 53–59, 33–37, 25–29, 7–10 respectively vs. 50–57, 44–52, 29–35, 23–27, and 5–8 in T. chefuensis), fewer branched anal-fin rays [24–27 vs. 24–30 (usually 27–29)], a deeper body (body depth 25.6–27.9% SL vs. 21.9–26.0%, the distance between the dorsal and anal fin origins 29.6–31.7% SL vs. 26.1–30.2%, and the caudal-peduncle depth 10.5–11.7% SL vs. 8.8–10.6%).

Lepadichthys coccinotaenia Regan 1921 (Gobiesocidae: Diademichthyinae) is redescribed on the basis of 60 specimens, including the holotype, and a new species of Lepadichthys, previously misidentified as L. coccinotaenia, described from Japan. Lepadichthys trishula sp. nov. is characterized by the following combination of characters: 10–12 (modally 11) dorsal-fin rays; 9–11 (10) anal-fin rays; 23–26 (23) pectoral-fin rays; upper end of gill membrane level with base of 8th to 10th (usually 10th) pectoral-fin ray in lateral view; 6–8 (7) gill rakers on each arch; 32 or 33 (32) vertebrae; snout somewhat short and slender, its length and depth 7.4–9.4 (mean 8.4) and 4.0–6.5 (5.1) % SL, respectively; upper jaw not sharply pointed or projected, its length 5.5–7.7 (6.5) % SL; side of lower-jaw teeth with hook-like tips; head depth 7.2–10.4 (8.5) % SL; disc size moderate, its length 14.0–18.2 (16.8) % SL; dorsal and anal fins with weak membranous connections to caudal fin; head sensory canal pores well developed, including 2 nasal, lacrimal and postorbital, and 3 preopercular pores; and three narrow white stripes from snout to vertical through posterior margin of disc, including two lateral and one on the dorsal midline. The new species is currently known only from Japan, whereas L. coccinotaenia occurs only in the southwestern Indian Ocean.

A new perchlet, Plectranthias ryukyuensis, is described on the basis of four specimens (41.2–61.6 mm standard length: SL) from the Okinawa Islands, Japan. Plectranthias ryukyuensis can be distinguished from all congeners by the following combination of characters: X, 15 or 16 dorsal-fin rays; 14 pectoral-fin rays, all unbranched; lateral line complete, with 29 or 30 pored scales; 3 scale rows above lateral line; 5 or 6 diagonal rows of large scales on cheek between eye and corner of preopercle; preopercle with two antrorse spines on ventral margin, 20–29 serrae on posterior margin; margins of subopercle and interopercle with a few serrae (weak in large individuals); minute flaps at tips of first to ninth dorsal-fin spines; caudal fin shallowly emarginate, with some ray branches distinctively elongated past fin margin; fourth dorsal-fin spine longest, its length 110.6–128.6% that of third spine; body pinkish-white with two longitudinal rows of irregular orange-red blotches on upper half of lateral surface when fresh (rows close together in smaller than ca. 50 mm SL), blotches interconnecting anteriorly on upper and lower rows, and posterior half of lower row; four faint orange-red vertical bands below lateral line on posterior half of body and two distinct yellow blotches on cheek in fresh specimens; body uniformly yellowish-brown with two longitudinal rows of irregular dark blotches on upper half of lateral surface in preserved specimens (faint in small specimens). A key to the Japanese species of Plectranthias is given.

A taxonomic review of the clingfish genus Kopua (Gobiesocidae: Trachelochisminae) in Japan recognizes three species: K. japonica Moore, Hutchins and Okamoto 2012, K. vermiculata Shinohara and Katayama 2015 and K. yoko sp. nov. Kopua japonica and K. vermiculata are redescribed with revised diagnoses on the basis of 20 specimens (10.4–30.4 mm standard length; SL) and the holotype, respectively. Kopua japonica is similar to K. vermiculata in head sensory pore characters (normally single nasal and postocular canal pores). However, the former differs distinctly from the latter as follows: 6–8 (modally 7) gill rakers (vs. 4 or 6); 31–33 (33) vertebrae (vs. 35); anus slightly closer to posterior margin of disc than to anal-fin origin (vs. much closer to posterior margin of disc); snout length 5.3–8.7 (mean 7.0) % SL (vs. 9.2 % SL); disc length 21.2–24.0 (22.8) % SL (vs. 18.8 % SL); pre-dorsal- and anal-fin lengths 72.9–78.4 (75.2) and 78.1–82.8 (80.1) % SL, respectively (vs. 67.5 and 73.6 % SL); and two stripes on cheek (vs. a triangular blotch). Kopua yoko sp. nov., based on 14 specimens (17.7–28.8 mm SL) from the Pacific coast of southern Japan, Sea of Japan and the East China Sea, is characterized by the following combination of characters: 6 or 7 (modally 6) dorsal-fin rays; 4–6 (5) anal-fin rays; 21 or 22 (21) pectoral-fin rays; 4–6 (5 or 6) gill rakers; 31–33 (31) vertebrae; a single (rarely two) nasal canal pores; two lacrimal and preopercular canal pores; snout length 6.5–7.9 (mean 7.1) % SL; gill opening depth 5.8–7.1 (6.5) % SL; least interorbital width 2.0–3.7 (2.6) % SL; disc length 20.3–25.0 (23.1) % SL, disc region D without flattened papillae; caudal-peduncle depth 8.1–10.2 (9.2) % SL; anus slightly closer to posterior margin of disc than to anal-fin origin; pre-dorsal- and anal-fin lengths 71.6–77.1 (73.9) and 77.0–83.7 (80.4) % SL, respectively; post-dorsal-caudal length 12.6–15.0 (13.8) % SL; arch-shaped blotches on lateral aspect of body; and two reddish-orange stripes on cheek. Morphological changes with growth in K. japonica and K. yoko sp. nov. are also described.

A new species of liparid fish Careproctus surugaensis is described from a single specimen collected between 1,450 and 1,570 m depth on the northern part of Suruga Trough, Suruga Bay, Japan. It can be distinguished from all currently recognized congeners by the following combination of characters: 50 total vertebrae, 47 dorsal-fin rays, 39 anal-fin rays, 32 pectoral-fin rays, 10 principal caudal-fin rays, pectoral proximal radials 4 (first to third with notches); trilobate teeth on both jaws, gill slit 7.1 % SL, extending in front of 7th pectoral fin ray base; maximum body depth 19.1 % SL, disk length 7.9 % SL, anus midway between posterior margin of pelvic disk and anal-fin origin; body and fins light orange except blackish peritoneum.

Taxonomic analysis of a group of morphologically similar and phylogenetically related ponyfishes (Perciformes: Leiognathidae) establishes the Equulites elongatus species group comprising three valid species: Equulites aethopos sp. nov., currently known only from southern Red Sea; Equulites elongatus (Gunther 1874), known from northern Australia, Indonesia and Myanmar; and Equulites popei (Whitley 1932), known from Japan, Philippines, Malaysia (Sabah), Thailand (Gulf of Thailand), Oman, the Red Sea, and Mozambique. Although E. popei has previously been regarded as a junior synonym of E. elongatus, the present mitochondrial DNA analysis revealed that these two nominal species are different and that they constitute a monophyletic group separate from other species of Equulites. The E. elongatus species group can be defined by the following of characters: slender body (20–30% in standard length), deeply incised posterior margin of the adipose eyelid, and ventral surface of breast completely scaly. Equulites aethopos sp. nov. differs from the other two species in having smaller eyes (eye diameter 53–68% of postorbital head length vs. 78–137%) and tips of neural and hemal spines of the fourth preural centrum distinctly expanding (vs. slightly expanding). Equulites elongatus is distinguished from E. popei by: scales above and below the lateral line 5–9 and 9–14, respectively (vs. 8–13 and 12–19), anus anteriorly located (distance from the pelvic-fin insertion to the center of anus 30–42% of the distance from the pelvic-fin insertion to the anal-fin origin vs. 35–50%), and more numerous dorsolateral dark marks (1–9 ring marks and 0–14 dark spots smaller than a half of pupil diameter vs. 0–2 and 0–5).

A new species of labrid fish Oxycheilinus samurai sp. nov. is described on the basis of five specimens from the Ryukyu Islands, Japan, and Panay Island, the Philippines. The new species is most similar to the Indo-West Pacific species Oxycheilinus orientalis in having a slender compressed body, 12 pectoral-fin rays, a blackish blotch around the anterior portion of the lateral-line anterior series, and a dark blotch basally on the membrane between the first and second dorsal-fin spines. However, O. samurai can be distinguished from O. orientalis by the following combination of characters: gill rakers 4 + 7–8; snout rounded with maximum circumference 49.8–63.5 % of standard length (SL); interorbital width 7.7–9.2 % of SL; caudal-peduncle depth 13.8–15.3 % of SL; posterior margin of caudal fin white; black or dark red area just before white posterior margin of caudal fin; poorly defined blackish blotches on inner surface of opercle in preserved specimens.

Rhinogobius similis Gill 1859, type species of the genus, is redescribed (with neotype designation) based on seven specimens collected from the putative type locality (Shimoda, Kanagawa Prefecture, Japan). The species, previously known as R. giurinus (Rutter 1897) (a junior synonym), can be distinguished from its congeners by having the following combination of characters: I, 8 second dorsal-fin rays; 18–19 pectoral-fin rays; 8–12 predorsal scales; 29–31 longitudinal scales; 11 + 15 = 26 vertebrae; predorsal squamation comprising large ctenoid scales, reaching anteriorly to near posterior margin of eye; 5–6 short transverse rows of sensory papillae ventral to eye; several short transverse rows of sensory papillae between two longitudinal rows of sensory papillae on cheek; a dark brownish gray reticulation or reddish oblique lines on head but not on its ventral surface; a black spot, as large as pupil, dorsoposteriorly on pectoral-fin base; a longitudinal series of alternating large and small black blotches on midlateral body; two to four irregular longitudinal rows of small sky-blue spots on midlateral body when alive.

A new owstoniine bandfish, Owstonia kamoharai, is described based on six specimens (147–402 mm in standard length) collected from off southern Japan: Shikoku Island, Kii Peninsula, and Suruga Bay. The new species differs from its congeners by the following combination of characters: dorsal-fin rays III, 21; anal-fin rays I, 14; pectoral-fin rays 21–23; total caudal-fin rays 17 (branched 13); vertebrae 28–29; gill rakers on first arch 39–40; cheek with 88–123 scales in 8–10 rows; lateral line without branch, not forming loop in front of dorsal fin, ending below 8th–10th dorsal-fin soft rays; scales in longitudinal rows 53–56; lower margin of preopercle smooth; pelvic fin short, not reaching to anus; posterior margin of caudal fin rounded; uniformly reddish coloration with black markings on membranes of both jaws; and white margins of vertical fins.

A new glyptosternine catfish, Creteuchiloglanis arunachalensis is described on the basis of a single specimen collected from the upper Brahmaputra River drainage, northeastern India. The new species is distinguished from its congeners by the following characters: shorter adipose-fin base (25.9 vs. 26.2–37.3 % standard length; SL) except C. longipectoralis; shorter maxillary barbel (71.2 vs. 75.2–99.8 % head length) except C. macropterus; and longer prepelvic (45.4 vs. 36.4–44.9 % SL) except C. brachypterus. It can be further differentiated by a combination of the following characters: pectoral fin not reaching pelvic-fin origin; pelvic fin not reaching at vertical through adipose-fin origin; pale patches on body except occipital region; absence of milky-white patch on the base of posterior end of maxillary barbel; longer post adipose distance (10.1 % SL); tip of rectal lobe obtusely rounded; caudal-fin lobes equal; posterior margin of caudal fin slightly convex; adipose-fin separate from caudal fin; and caudal fin with broad bean-shaped medial band.

Two new atherinid fishes, Hypoatherina golanii and Hypoatherina lunata, are described based on specimens collected from the wide range of the Indo-West Pacific. The former species is known from the Red Sea and was confused with Hypoatherina barnesi because it has a somewhat wide midlateral band and overlapping meristic counts. Hypoatherina golanii is distinguished from its congeners by the midlateral scales with an indented posterior margin, posterior margin of anterior predorsal scales with a spatular outgrowth, posterior margin of axillary scales without a distinct projection, and posterior end of maxilla not slanted downward. Hypoatherina lunata is distributed in the waters of southern Japan (Okinawa and Kagoshima prefectures) and Indonesia (North Sulawesi, Maluku, and Papua), but was confused with Hypoatherina woodwardi. Hypoatherina lunata is distinguished from its congeners in having a distinct crescent marking in front of the eye and the anus usually situated anterior to the tip of the pelvic fin.

The myrophine ophichthid fishes (worm eels) Muraenichthys aoki Jordan and Snyder 1901 and Muraenichthys gymnotus Bleeker 1857 are redescribed as valid species of Scolecenchelys based on the types and non-type specimens collected from the Indo-Pacific. Because both species are similar to each other in having acute snouts, the posterior margin of the eye before the rictus, and their dorsal-fin origins located slightly posterior to a vertical line through the anus, Scolecenchelys aoki has usually been regarded as a junior synonym of Scolecenchelys gymnota. However, S. aoki is clearly distinguishable from S. gymnota by having a median groove on the ventral side of snout (absent in S. gymnota), uniserial maxillary teeth in smaller specimens (

A new species of the fish genus Grammonus (Ophidiiformes: Bythitidae) is described based on a ripe female, 98 mm in standard length (SL). It was caught at the bottom of a cave at a depth of 20 m under lightless conditions in Ie-shima Island, one of the Ryukyu Islands. A comparison to the seven described species of Grammonus shows the greatest similarity to the widely distributed G. robustus, but G. yunokawai n. sp. differs from it by having fewer vertebrae (41 vs. 44–47), a greater predorsal length (41.5 vs. 32.0–39.0% SL), higher posterior margin of maxilla (8.4 vs. 5.6–7.3% SL), and greater interorbital width (10.5 vs. 5.9–7.6% SL).

Evoxymetopon macrophthalmus sp. nov. is described on the basis of a single specimen collected off Okinawa Island, Ryukyu Islands, Japan. Among the two valid species of Evoxymetopon, the new species is more similar to E. poeyi in having the first dorsal-fin spine enormously large, compressed, and sword shaped. It differs from E. poeyi in having the upper profile of head uniformly convex without a prominent sagittal crest (vs. with a prominent sagittal crest), tip of first anal pterygiophore connected to the last rib in the anterior part, while the first hemal spine is long and connected to the posterior margin of pterygiophore bone plate (vs. connected to the first hemal spine only), a larger eye, 4.5 times in head length (vs. 5.5–5.9 times), 15 externally visible anal-fin soft rays (vs. 20), 9 upper gill rakers of the first arch (vs. 4–6), and 60 caudal vertebrae (vs. 64).

A trichiurid, Lepturacanthus roelandti (Bleeker, 1860), previously regarded as a synonym of L. savala (Cuvier, 1829), is redescribed as a valid species on the basis of the holotype of the former and four non-type specimens. This species differs from the two valid congeners, viz., L. savala and L. pantului (Gupta, 1966), in having a gold sheen or yellowish-silver color when fresh (vs. steel-blue with metallic sheen in the latter two), posterior margin of maxilla reaching or extending beyond a vertical through hind eye margin (vs. not extending beyond a vertical through hind eye margin), pectoral fin slightly longer than snout (vs. slightly shorter than snout), tip of pectoral fin clearly extending beyond dorsal outline when vertically orientated (vs. not reaching dorsal outline), gill rakers absent or reduced to stiff ossified structures (vs. well developed, spinelike), first anal fin spine situated below the 40th–43rd dorsal fin ray (vs. below 35th–39th in L. pantului and 35th–40th in L. savala), precaudal vertebrae 42–43 (vs. 35–39 in L. pantului and 36–40 in L. savala), and attaining larger sizes [882–1200 mm in total length (TL) vs. less than 800 mm TL in the latter two].

Trichiurus australis, a new trichiurid fish, is described on the basis of four specimens collected off Burnett River mouth, Pialba and Thursday Island, Queensland, Australia. The new species strongly resembles Trichiurus brevis Wang and You, 1992 (distributed in the South China Sea), T. russelli Dutt and Thankam, 1967 (the northwestern Bay of Bengal and the northern Gulf of Thailand), and T. nickolensis Burhanuddin and Iwatsuki, 2003 (northwestern Australia) in having the highest point of the supraoccipital crest situated directly above the posterior margin of the eye and being relatively small in size (less than ca. 700 mm in total length: TL). It differs from those three species in having spinescent gill rakers almost with 2 equally long cusps [vs. (1, rarely 2 but 1 of them clearly shorter than another)], posterior caudal peduncle vertebrae bearing neural spines (vs. neural spines absent), longer caudal peduncle length (mean 16% TL vs. 6% in T. brevis, 8% in T. nickolensis, and 8% in T. russelli), and shorter precaudal length (83% vs. 93%, 91%, and 91%), preanal length (26% vs. 33%, 31%, and 35%), and head length (9% vs. 12%, 11%, and 13%). We have tentatively classified this new species under the “Trichiurus russelli complex” because the foregoing diagnostic characters are identical to this species complex except for the presence of neural spines in the posterior caudal vertebrae.

The holotype of Lycenchelys melanostomias Toyoshima, 1983, the original description of L. brevimaxillaris Toyoshima, 1985, and 54 Lycenchelys specimens from the Okhotsk Sea and the Pacific off northern Japan were compared. Lycenchelys brevimaxillaris was distinguished from L. melanostomias in having 4 postorbital pores, pale-colored stomach, and smaller mouth in the original description (vs. 5 postorbital pores, dark stomach, and larger mouth in L. melanostomias). However, L. melanostomias has 4 or 5 postorbital pores, as recently pointed out. The coloration of the stomach of the L. melanostomias holotype and the new material is pale. Meristic counts and proportional measurements of the new material include those of the type specimens of both species. The length of upper jaw exhibits sexual dimorphism in L. melanostomias larger than ca. 170 mm TL: upper jaw reaching near posterior margin of pupil in males vs. near middle of eye in females. The L. brevimaxillaris holotype (female) agrees well with female L. melanostomias in this character. These facts indicate that L. melanostomias is a senior synonym of L. brevimaxillaris.

A taxonomic review of seven-spined Polynemus species recognizes two species as valid: P. hornadayi Myers, 1936, currently known only from western Sarawak, Kalimantan, Malaysia, and P. paradiseus Linnaeus, 1758, distributed from India to Thailand and regarded as a senior synonym of P. aureus Hamilton, 1822, P. longifilis Cuvier in Cuvier and Valenciennes, 1829, P. risua Hamilton, 1822, and P. toposui Hamilton, 1822. Polynemus hornadayi differs from P. paradiseus in having a strongly protruded occipital profile (vs. nearly straight in the latter), lower counts of anal fin soft rays (mode 11 vs. 12) and gill rakers (26 vs. 32 or 33), higher counts of pectoral fin rays (18 vs. 17), scales above and below the lateral line (11 and 18 vs. 7 and 11, respectively), and pored lateral line scales (94 vs. 70), the fifth pectoral filament longest (vs. sixth), the fourth pectoral filament longer (extending well beyond the posterior central margin of the caudal fin vs. not reaching posterior central margin), a longer pectoral fin ray (posterior tip of pectoral fin reaching to midpoint of anal fin base vs. not reaching), a deeper maxilla posterior margin (mean 5% of SL vs. 4% of SL), and a well-developed swimbladder (vs. absent).

The gerreid species,Gerres baconensis (Evermann & Seale),G. equulus Temminck & Schlegel andG. oyena (Forsskal), were re-assessed as valid following examination of their holotypes and other specimens, and included in the “G. oyena complex”.Gerres haconensis is currently known only from Bacon, Luzon Island, Philippines and the Ogasawara (=Bonin) Islands, Japan, andG. equulus only from southern Japan (except Ryukyu Islands) and southern Korea.Gerres oyena is widely distributed in the Indo-West Pacific (in Japan, only from the Ryukyu Islands).Gerres baconensis differs from bothG. equulus andG. oyena in having higher counts of both the pored lateral line scales (39–42 vs 35–41 in the latter two species) and the lower gill raker series (8 or 9 vs. usually 7). A U-shaped premaxillary groove, formed on the dorsum of the forehead by the long ascending processes of the premaxillae, is scaleless inG. equulus andG. oyena, whereas it is fully scaled just behind the level of the posterior nostrils inG. baconensis over ca. 160 mm in standard length (SL) (partially scaled in specimens of ca. 100 mm SL).Gerres equulus differs fromG. oyena in having the posterior margin of the maxilla not extending beyond a vertical through the anterior margin of the inner dermal eye opening, shorter second dorsal and anal fin spines (means 18.5% and 8.5% of SL, respectively vs. 21.2% and 10.3% of SL), lower body depth at first anal fin spine base (27.0% vs. 29.6% of SL) and dorsomedial U-shaped groove scaleles throughout life (vs. tiny squamation anteriorly in specimens over ca. 130 mm SL). OtherGerres species of uncertain status and/or related species are discussed.

Gazza dentex (Valenciennes in Cuvier and Valenciennes, 1835), having been synonymized withG. minuta (Bloch, 1795), is redescribed as a valid species.Gazza dentex differs fromG. minuta in having deeper body (43.6–51.4% of standard length [SL] vs. 28.3–46.5% of SL), a broad anterodorsal extension of subocular silvery region, in contact with orbit proximally and distally (vs. a long narrow anterodorsal extension, proximal contact only with orbit), scaled area of anterior dorsolateral suface of body not beyond a vertical through posterior tip of sensory canal on temporal (vs. beyond), distance from posterior margin of temporal to anterior tip of dorsolateral scaled area equal to length of 3–5 anterior pored lateral line scales (vs. length of 1–2.5 anterior pored lateral line scales), some dark narrow wavy bands dorsolaterally on body (vs. some dark broad wavy bands above lateral line and a row of dark spots along lateral line), first interneural inserted deeply between first and second neural spines (vs. inserted shallowly), anterior expansion of first interneural narrow, its margin concave (vs. anterior expansion broad, its margin broadly convex), antrorse extension of first interhemal short, deep, acutely pointed (vs. long, moderately deep, pointed) first to fourth hypurals forming 2 plates (first+second and third-fourth hypurals) (vs. a single plate). The lectotype and three paralectotypes are designated forG. dentex, andG. minuta is redescribed.

Osteological and myological studies on the caudal complex of flying fishes (Exocoetidae) plusOxyporhamphus (of Hemiramphidae) revealed the following shared derived conditions: 1) neural spines of preural vertebrae broader than haemal spines; 2) spur present on posterior margin of preural vertebra 2;3) upper hypural plates steeply angled; 4) lower hypural plate extending strongly posteriorly; 5) lower hypural plate deeply surrounded by caudal fin rays; 6) flexor ventralis well developed, arising from neural spines; 7) flexor ventralis externus well developed; 8) adductor dorsalis well developed.Oxyporhamphus and exocoetids also share a lower jaw of adults not elongate and the premaxilla with a straight anterior margin. Therefore,Oxyporhamphus is transferred to the Exocoetidae, with which it shares a total of 10 derived conditions.

A new bothid flounder,Arnoglossus micrommatus, is described from the southwestern coast of Australia (off Albany, Western Australia). This species is distinguished from other species ofArnoglossus by combination of the following characters: gill-rakers serrated on posterior margin; upper jaw length 2.83–3.12 in head length (HL); upper eye diameter 4.17–5.51 in HL; scales in lateral line 52–62; vertebrae 11+28−29=3t-40.