Search

Rhinogobius sp. YB (Gobiidae) distributed in the Ryukyu Archipelago is a fluvial species of gobies. We present 34 novel microsatellite loci that were tested on 32 individuals from the Okierabu-jima Island in Kagoshima Prefecture. Seventeen loci were polymorphic, while the remaining 17 were monomorphic. The number of alleles per the polymorphic loci ranged from 2 to 15. The observed heterozygosities ranged from 0.038 to 1.000 and the expected heterozygosities varied from 0.038 to 0.816. These microsatellite loci will enhance future investigations on the genetic differentiation and structure of populations of R. sp. YB.

Pempheris ufuagari sp. nov. is described based on 10 specimens, 143.9–196.8 mm in standard length, collected from Mi-nami Daito Island and Ogasawara Islands, which are oceanic islands of Japan. Pempheris ufuagari is characterized by a distinct black spot on the pectoral fin base, a bright yellow dorsal and caudal fin, and a blackish band on the outer margin of the anal fin. Pempheris oualensis also has a large body and a distinct black spot on the pectoral fin base, and forms mixed schools with P. ufuagari, but can be distinguished by the different fin coloration (dorsal and caudal fin brown or pale; no blackish band on anal fin margin), and the presence of a villiform tooth band extending outside the lips. Although P. otaitensis, which is found in French Polynesia and Samoa, has similar coloration as P. ufuagari, the latter has lower scale counts than those of the former species: pored lateral-line scales 62–71 (vs. 70–79); scale rows above lateral line 6 1/2–7 1/2 (vs. 8 1/2); predorsal scales 37–43 (vs. 44–48).

The eel goby, genus Taenioides (Gobiidae: Amblyopinae), inhabits muddy bottoms of estuaries or shallow areas of seas in the Indo-Pacific Ocean. Among congeners, T. cirratus ( Blyth, 1860 ) has been thought to be distributed in Japan, but taxonomic confusions remain as to which scientific names are applicable to Japanese Taenioides species, or more fundamentally, how many Taenioides species are distributed in Japan, due in part to the rarity of this group in museum collections and the morphological similarity among species. To clarify the species diversity of the genus Taenioides in Japan, we conducted phylogenetic analysis on the basis of partial mitochondrial DNA sequences and morphological observation of more than 100 specimens. As a result, four distinct species were distinguished from each other, on the basis of both genetic divergences (2.9-5.7%, 16S rRNA gene) and morphological differences (i.e., degree of development of dermal folds on the head, numbers of barbels and vertebrae). Although the identifications of four species need additional verifications, they were identified as T. anguillaris, T. snyderi, T. gracilis and T. cf. kentalleni, and the species name T. cirratus does not seem to be appropriate to any of four detected species. Museum collections indicate that the two species, which are distributed in the main islands of Japan, were collected frequently and treated as a single species. The other two were each collected only from a single locality of Okinawa Island in this study, of which one seems to be uncommon worldwide as well.

The extremely paedomorphic fish Schindleria (Gobioidei, Schindleriidae) is widely distributed in the Indo- Pacific Ocean, inhabiting coral reef lagoons. At least 21 cryptic species (Schindleria spp. 1-21) have been discov- ered around the Ryukyu and Ogasawara Islands. As a first step in extending the survey areas to the entire Indo-Pacific Ocean, the present study collected and examined Schindle- ria in Palau, located approximately 2,200 km from the Ryukyu Islands, for any cryptic diversity. Molecular phy- logenetic analysis using partial mitochondrial 16S rRNA sequences of 71 specimens revealed four new cryptic spe- cies of Schindleria spp. 22-25 (Palau 1-4) in Palau.

The authorship of Platycephalus japonicus and Platycephalus crocodilus is researched. Although many authors have considered that the authorship of these flatheads can be attributed to Tilesius (1812), we consider that Cuvier in Cuvier and Valenciennes [ex Tilesius] (1829) has valid authorship of them. Platycephalus isacanthus, Platycephalus borboniensis and Platycephalus guttatus were also established by Cuvier in the same publication. The conspecificity of these three species and the precedence of P. japonicus are reconfirmed in this study. Although many authors have recognized the validity of P. guttatus, its holotype is identical to P. crocodilus. We also establish the precedence of P. crocodilus over P. guttatus.

Two morphologically similar species of gizzard shad, Nematalosa japonica Regan and N. come (Richardson), sympatrically distributed off Okinawa Island, Japan, were examined using an allozyme locus (SOD*) and two nuclear polymerase chain reaction (PCR)-based DNA markers (ITS-1 and CaM), which provided diagnostic identification of each species. In addition, a multiplex PCR-based mitochondrial DNA (mtDNA) marker (16S) was used to characterize the distribution of mtDNA haplotypes among specimens. The species composition of sympatric and allopatric population samples from Tungkang, southern Taiwan, to Okinawa and the Shikoku Islands, Japan, were also examined. Gizzard shad with hybrid genotypes were detected in three populations from Okinawa Island, with hybrid frequency ranging from 1 to 67%. A backcross level of 2% was detected in the dominant hybrid frequencies of one population sample only. Morphological examination of hybrids showed intermediate forms, with hybrid indices of three meristic characters falling between those of the parental species (range 39–53; mean 45). Although principal component analysis showed differences between N. japonica and N. come based on the first principal component scores, hybrids were difficult to identify. Accordingly, satisfactory identification of species and hybrids could be achieved only using genetic tools. We also discuss the cause of hybridization and its relationship with recently conducted reclamation on Okinawa Island.

Several groups of marine fishes and squids form mutualistic bioluminescent symbioses with luminous bacteria. The dependence of the animal on its symbiont for light production, the animal's specialized anatomical adaptations for harboring bacteria and controlling light emission, and the host family bacterial species specificity characteristic of these associations suggest that bioluminescent symbioses are tightly coupled associations that might involve coevolutionary interactions. Consistent with this possibility, evidence of parallel cladogenesis has been reported for squid–bacterial associations. However, genetic adaptations in the bacteria necessary for and specific to symbiosis have not been identified, and unlike obligate endosymbiotic associations in which the bacteria are transferred vertically, bacterially bioluminescent hosts acquire their light-organ symbionts from the environment with each new host generation. These contrasting observations led us to test the hypotheses of species specificity and codivergence in bioluminescent symbioses, using an extensive sampling of naturally formed associations. Thirty-five species of fish in seven teleost families (Chlorophthalmidae, Macrouridae, Moridae, Trachichthyidae, Monocentridae, Acropomatidae, Leiognathidae) and their light-organ bacteria were examined. Phylogenetic analysis of a taxonomically broad sampling of associations was based on mitochondrial 16S rRNA and cytochrome oxidase I gene sequences for the fish and on recA, gyrB and luxA sequences for bacteria isolated from the light organs of these specimens. In a fine-scale test focused on Leiognathidae, phylogenetic analysis was based also on histone H3 subunit and 28S rRNA gene sequences for the fish and on gyrB, luxA, luxB, luxF and luxE sequences for the bacteria. Deep divergences were revealed among the fishes, and clear resolution was obtained between clades of the bacteria. In several associations, bacterial species identities contradicted strict host family bacterial species specificity. Furthermore, the fish and bacterial phylogenies exhibited no meaningful topological congruence; evolutionary divergence of host fishes was not matched by a similar pattern of diversification in the symbiotic bacteria. Re-analysis of data reported for squids and their luminous bacteria also revealed no convincing evidence of codivergence. These results refute the hypothesis of strict host family bacterial species specificity and the hypothesis of codivergence in bioluminescent symbioses. © The Willi Hennig Society 2007.

Phylogenetic relationships of rabbitfishes (the family Siganidae), ecologically important components as primary consumers in coral reef communities, were studied using mitochondrial cytochrome b gene and nuclear ITS1 (internal transcribed spacer 1) sequence analyses. The analyses of 19 out of 22 species known in the Western Pacific region revealed that siganids are genetically clustered into three major clades, which are characterized by some morphological and ecological traits. Between closely related species, such as Siganus guttatus-S. lineatus and S. virgatus-S. doliatus, and also between two morphs recognized in S. corallinus, small but discernible genetic differentiation was found, implying that the components of each pair are incipient species. On the other hand, between some species, such as S. fuscescens-S. canaliculatus and S. unimaculatus-S.vulpinus, individuals of the components of each pair were found to construct a genetic mosaic, suggesting that the components are genetic color morphs within a single biological species, respectively. Moreover, evidence from morphological characters, mtDNA, and nuclear DNA gave an inconsistent picture of identity and relationships for several individuals. They were regarded as hybrids or individuals with hybrid origin. Such instances were observed not only between closely related species, such as S. guttatus-S. lineatus, S. virgatus-S. doliatus, and two morphs (incipient species) in S. corallinus, respectively, but also between distantly related ones, such as S. corallinus-S. puellus. In fact, more than half of the species examined (11/20, when treating the two morphs in S. corallinus as independent species) were involved in hybridization. These suggest that hybridization is much more prevalent in marine fishes than previously assumed, and may have some relevance to their diversification.

Gerres japonicus Bleeker, 1854, and Gerres subfasciatus Cuvier in Cuvier and Valenciennes, 1830, are redescribed, and Gerres akazakii sp. nov. (Japanese endemic), Gerres ryukyuensis sp. nov. (Okinawa I., Japan), and Gerres shima sp. nov. (Indo-Malayan region, including the Andaman Sea, Southeast Asia, southern China and Taiwan, and Ryukyu Is., Japan) are described. Gerres ovatus Gunther, 1859, and Gerres kapas Bleeker, 1854, are recognized as junior synonyms of G. subfasciatus and Gerres oyena (Forsskal, 1775), respectively. All species (except G. oyena) have a small (

The Indo-Pacific marine atherinid fishes Atherinomorus forskalii (Ruppell, 1838), Atherinomorus lacunosus (Forster, 1801), and Atherinomorus pinguis (Lacepede, 1803) are redescribed as valid species based on the types and non-type specimens collected throughout the Indo-Pacific. They are similar to each other chiefly in having a wide midlateral band (almost the same or greater than the midlateral scale width), large mouth (posterior tip of upper jaw reaching to or beyond a vertical through anterior margin of pupil), and no distinct tubercle at the posterior end of the dentary. All three species are distinguishable from congeners by those characters. The three species have long been confused with each other or synonymized erroneously as a single species. Atherinomorus forskalii, known from the Red Sea and eastern Mediterranean, differs from Atherinomorus lacunosus and Atherinomorus pinguis in having conspicuous, large endopterygoid teeth, forming obvious tooth ridges. Atherinomorus lacunosus, widely distributed in almost the entire Indo-Pacific, from East Africa to Tonga, north to southern Japan, and south to northern Australia, differs from Atherinomorus pinguis in having a wider midlateral band (the lower margin reaching to almost the center of the fourth scale row at level of the anal fin origin vs. the lower margin reaching to the ventral end of the third scale row in Atherinomorus pinguis) and more numerous midlateral scales (40–44 vs. 38–41 in Atherinomorus pinguis). Atherina morrisi Jordan and Starks, 1906, Hepsetia pinguis mineri Nichols and Roemhild, 1951, Pranesus capricornensis Woodland, 1961, Pranesus maculatus Taylor, 1964, and Pranesus pinguis ruppelli Smith, 1965, are regarded as junior synonyms of Atherinomorus lacunosus. Atherinomorus pinguis is also widely distributed in the Indo-West Pacific, from East Africa to northern Australia and north to southern Japan. Atherina pectoralis Valenciennes, 1835, is considered a junior synonym of Atherinomorus pinguis.

There are no significant morphological differences between the four syntypes of the pinguipedid sandperch Percis caudimaculatum Haly, 1875 and the holotype of Parapercis ommatura Jordan and Snyder, 1902. The former nominal taxon is thus a subjective senior synonym of the latter, but it is also a junior homonym of Percis caudimaculata Rüppell, 1838, and thus invalid. In addition, Rüppell's taxon, now assigned to the genus Parapercis, has been recognized as a junior synonym of Parapercis hexophtalma (Cuvier in Cuvier and Valenciennes, 1829). Parapercis ommatura, being the first available junior synonym of Parapercis caudimaculata (Haly, 1875), becomes the valid name for the species.

The western Pacific marine clupeoid fish, Spratelloides atrofasciatus Schultz, 1943, previously regarded as a synonym of S. gracilis (Temminck and Schlegel, 1846), is redescribed here as a valid species on the basis of the holotype and 115 non-type specimens collected from the Ryukyu Islands. Both S. atrofasciatus and S. gracilis are similar chiefly in having a midlateral band that does not fade anteriorly. S. atrofasciatus differs from Spratelloides gracilis in having fewer anal fin rays, pectoral fin rays, vertebrae and gillrakers. Spratelloides atrofasciatus also has a shorter head length, a shorter upper jaw length, a shorter snout length, a wider lateral band equal to the eye diameter; numerous black pigment spots on the inner side of the gill opening that are visible from the outside in preserved specimens (vs not visible in S. gracilis). The two species are sympatrically distributed in the Ryukyu Islands. Spratelloides atrofasciatus matures from 32 mm SL and grows to a known maximum size of 45mm SL, while S. gracilis matures from about 50 mm SL and grows to over 100 mm SL.

A new sparid species, Acanthopagrus akazakii, is described on the basis of 12 types collected from Noumea, New Caledonia. Acanthopagrus akazakii is most similar to Acanthopagrus berda in overall appearance but differs from the latter in having 41/2 scale rows between the 5th dorsal fin spine base and lateral line, anteriormost head scales broadly rounded without small scales anteriorly, upward- and downward-oriented portions present on anteriormost part of upper lip, a downward-oriented portion on anteriormost part of lower lip in specimens over ca. 160 mm in standard length, and upper head profile gently convex from snout tip to above eye throughout growth (vs. 31/2 scale rows between 5th dorsal fin spine base and lateral line, anteriormost head scales rounded with small scales anteriorly, no upward and downward portions in anteriormost upper and lower lips, and upper head profile becoming concave from snout tip to above eye with growth). Furthermore, A. berda develops a strong concavity of the ventral edge of the first two infraorbitals above the posterior part of upper jaw with growth, whereas A. akazakii has a generally straight series throughout growth. Nominal species in A. berda are reviewed, with notes on nominal species of Acanthopagrus.

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).

Taxonomic analysis of a group of morphologically similar ponyfishes (Perciformes: Leiognathidae) establishes the Leiognathus splendens complex comprising four valid species: L. jonesi James, 1971, widely distributed in the Indo-West Pacific, from Mauritius to Papua New Guinea, north to Hainan I. (China), and south to Brisbane, Australia; L. kupanensis sp. nov., currently known only from Kupang, Timor, Indonesia; L. rapsoni Munro, 1964, currently known only from India, Indonesia, and Papua New Guinea, and L. splendens Cuvier, 1829, widely distributed in the eastern Indian and western Pacific oceans, from India to Papua New Guinea, and from southern Japan to northern Australia. The L. splendens complex can be defined by the following combination of characters: body depth 42-60% of standard length; mouth protruding downward; slender, minute teeth uniserially on jaws; lower margin of orbit above the horizontal through the gape when mouth closed; breast almost completely scaled; lateral line complete, and a dark blotch on top of spinous dorsal fin. Diagnostic characters of the members are as follows: L. jonesi—anterior dorsolateral body surface with a semicir- cular naked area on nape, and a paler dark blotch on spinous dorsal fin; L. kupanensis—anterior dorsolateral body surface widely naked; L. rapsoni—cheek scaled; L. splendens—anterior dorsolateral body surface completely scaled and a jet black blotch on spinous dorsal fin.

The fluviatile Rhinogobius sp. 1 (hereinafter R. sp. 1) (Japanese name kibara-yoshinobori or English name yellow belly medium-egg type) is broadly distributed in the Ryukyu Islands ranging from Amami-oshima Island to Iriomote Island. However, based on the molecular evidence, this species has probably had multiple origins from amphidromous species. We compared the coloration of specimens at Amami-oshima I. with that of the other specimens (islands) in the Ryukyu Is. Amami-oshima I. specimens of R. sp. 1 were different from the specimens of other populations in having five to six cross lines on the caudal fin. We examined the early life history of fluviatile Rhinogobius at Amami-oshima I., based on rearing experiments, and estimated the age of wild specimens by counting otolith increments. Spawned egg capsules of “Rhinogobius sp. 1” at Amami-oshima I. were larger than those of amphidromous species. Their developmental stage in newly hatched larvae was similar to that of Okinawan R. sp. 1 in having a straight notochord; however, it had a flexed notochord earlier than that of Rhinogobius sp. 2 (hereinafter R. sp. 2) (aobara-yoshinobori or blue belly medium-egg type). The ontogenetic trajectory of “Rhinogobius sp. 1” in Amami-oshima I. was similar to Okinawan R. sp. 1 (30 days in larval duration) but different from R. sp. 2 (15 days). In amphidromous relatives of R. sp. 2, developmental timing during larval period was earlier than in the amphidromous relatives of R. sp. 1. It has been suggested that the phenomenon of fluvial landlocking has been accompanied somewhat by egg size increase (on the basis of a few examples). However, the ontogenetic trajectories of fluviatile Rhinogobius species may be a reflection of those of ancestral amphidromous species.

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).

A new terapontid fish, Mesopristes iravi, is described based on 13 specimens collected on Iriomote Island, the Ryukyu Islands, Japan. This species closely resembles M. argenteus (Cuvier in Cuvier and Valenciennes, 1829) in having dark stripes on the body, but differs from that species in retaining the stripes even in adults (vs. stripes disappearing ontogenetically in the latter species), having the median stripe passing through the eye interrupted on the postorbital region (vs. continuous when the stripe present), a shorter fifth (longest) dorsal spine (14.6–19.7% SL vs. 18.0–22.2% SL), and a longer postorbital length (40.0–43.0% HL vs. 37.8–40.7% HL). Mesopristes iravi has been confused with M. argenteus in previous reports, and on the basis of the literature it may extend from the Ryukyu Islands, Japan, southward to Borneo, Indonesia, and New Guinea.

Atherinomorus aetholepis sp. nov. is described from the holotype and 51 paratypes, 44–72 mm in standard length, collected from Indonesian and Philippine waters. The species is similar to other congeners in general body appearance, especially A. duodecimalis and A. regina, in having a slender body, a tubercle on the posterior end of the dentary, and a narrow midlateral band, but clearly differing from them in having a long spatular outgrowth on the posterior margins of most of the predorsal and interdorsal scales. Additionally, the species differs from A. duodecimalis in having a more slender body [body depth 17–22 (mean 19) % SL vs. 19–25 (mean 22) % SL], more midlateral scales [37–40 (mean 38.4) vs. 35–38 (mean 36.6)], more total vertebrae [38–42 (mean 39.9) vs. 36–40 (mean 38.0)], and fewer lower gill rakers [18–22 (mean 20.2) vs. 20–25 (mean 22.3)], and from A. regina in having more anal fin soft rays (12–14 vs. 9–10).

Extremely small animals including fishes have been reported with discussion of the causes and consequences of their miniaturization. Here we demonstrate, for the first time, very early (i.e., 23–60 days old and 42–67 days old) sexual maturity in two groups of gobioid fishes (Schindleria and Paedogobius, respectively) in warm water, based on the otolith increments. The generation time of Schindleria is the shortest known among vertebrates under natural conditions. We discuss the occurrence and evolutionary significance of the progenesis found in gobioid fishes.

The taxonomic status of three small [probably less than ca. 600 mm in the largest total length (TL)] and poorly known species, Trichiurus brevis Wang and You, 1992 and T. minor Li, 1992, both from South China Sea, and T. russelli Dutt and Thankam, 1966, from Bengal Bay, was reexamined. Trichiurus brevis and T. russelli, being valid species, are redescribed and a neotype is designated for the latter. Trichiurus brevis is considered to be a senior synonym of T. minor, there being no significant differences in their type specimens. Both valid species, i.e., T. brevis and T. russelli, are similar to T. lepturus Linnaeus, 1758 (larger than ca. 1000 mm TL) in general appearance, but clearly differ from the latter in having the top of the supraoccipital crest situated directly above the posterior margin of eye (vs. well behind posterior margin), lower number of total vertebrae (147–155 and 149–153, respectively, in the former two species vs. 168–173 in T. lepturus), longer dorsal fin base (mean 87% and mean 84% vs. mean 76% of TL), and shorter caudal peduncle length (6% and 8% vs. 13% of TL). Furthermore, the former two species are characterized by having the anal fin origin situated below about the 32nd–35th dorsal fin ray base, whereas in T. lepturus it is situated below the 37th–41st dorsal fin ray base. We recognize that T. brevis and T. russelli together comprise a species group, defined as the “T. russelli complex,” in the genus Trichiurus, the two species differing in snout shape (strongly pointed in T. brevis vs. moderately pointed in T. russelli), snout length [mean 35% vs. mean 30% of head length (HL)], preopercle length (22% vs. 19% HL), predorsal length (70% vs. 63% HL), and dermal eye opening (16% vs. 18% HL).

Gerres microphthalmus sp. nov., described on the basis of the holotype and 38 paratypes, has a limited distribution in Japan, including Tanega Island, southeastern Kyushu, southern Shikoku, and southern Kii Peninsula, central Honshu. It has not been recorded from the Ryukyu Islands. The species is the fourth member of the “G. filamentosus complex,” characterized by an elongated second dorsal fin spine, the others being G. filamentosus, G. infasciatus, and G. macracanthus. Gerres microphthalmus sp. nov. is most similar to G. filamentosus in overall body appearance, but differs from the latter in having smaller eyes (8%–11% of standard length vs. 10%–16% in the latter), a higher orbit diameter ratio (as % of snout length) (93%–143% of snout vs. 71%–104% of snout), and fewer pored lateral line scales (40–43 vs. 43–46). The limited distribution pattern of the new species is discussed with G. equulus and Lates japonicus (Centropomidae) having a limited distribution similar to that of the new species.

A taxonomic revision of the polynemid fish genus Eleutheronema, which is redefined, resulted in three species of the genus being regarded as valid: Eleutheronema rhadinum (Jordan and Evermann, 1902), having to date been treated as a junior synonym of E. tetradactylum (Shaw, 1804) and currently known only from East Asia (China and Japan) where it is endemic; E. tetradactylum, a senior synonym of both Polynemus teria Hamilton, 1822 and Polynemus coecus Macleay, 1878, being a widely distributed Indo-West Pacific species, which ranges from the Persian Gulf to Australia; and E. tridactylum (Bleeker, 1845), distributed in Southeast Asia (Thailand, Malaysia, and Indonesia). Eleutheronema tridactylum is easily distinguished from both E. rhadinum and E. tetradactylum owing to the vomer lacking tooth plates in the former [vs. vomer with 2 deciduous tooth plates (in specimens at least over ca. 70 mm SL) in the latter] and lower counts of pectoral filaments (free lower rays, 3 vs. 4) and gill rakers [mode 8 (range 4–10) vs. 12 (10–17) and 13 (6–18) in E. rhadinum and E. tetradactylum, respectively]. Eleutheronema rhadinum clearly differs from E. tetradactylum in having higher counts of pored lateral line scales [mode 95 (range 82–95) vs. 73 (71–80) in the latter] and higher scale counts above and below the lateral line [12 (11–14) and 16 (15–17), respectively, vs. 10 (9–12) and 14 (13–15), respectively]. Furthermore, E. rhadinum is distinguished from E. tetradactylum by having a dense black pectoral fin [vs. vivid yellow in life (except in specimens over ca. 350 mm SL, pectoral fin dusky-yellow) in the latter]. Intraspecific variations and morphological changes with growth of the three species are also discussed.

Four species of the fish genus Pempheris are recognized for the Red Sea: P. adusta Bleeker, 1877; P. mangula Cuvier, 1829; P. nesogallica Cuvier in CuvierValenciennes, 1831; and a new species P. tominagai. All are wide-ranging in the western Indian Ocean, and P. mangula has migrated via the Suez Canal to the eastern Mediterranean Sea. Morphological and genetic analysis of 15 species in this genus show that P. adusta, a widely distributed species, that can't be divided into different species, because of the continuity of morphologies and distribution, and lack of variance in genetics between Indian Ocean, Red Sea, and Pacific Ocean populations. This confirms that the two subspecies described by Randall et al. (2013) are both synonyms of P. adusta. Pempheris adusta is distinguished from other species by a blackish spot on pectoral fin base, pored lateral-line scales 56-64, scale rows above lateral line 4 1/2-6 1/2, distinct blackish band on outer edge of anal fin, and blackish band on posterior edge of caudal fin. Pempheris mangula was named by Cuvier (1829) in a footnote making reference to a drawing and short description in Russell (1803) of a Pempheris from southeast India, giving only the native name ''Mangula-Kutti'', and listing no specimen. The wide distribution of this species, from the Indian Ocean to the Red Sea is also demonstrated by morphological and genetic analysis. Thus, the specimen collected from southern India is herein designated as the neotype. This species is distinguished from other species by its huge eye, deep body, blackish tip of the dorsal fin, pored lateral-line scales 49-60, and scale rows above lateral line 4 1/2-5 1/2. The extant syntype of KossmannRäuber's P. rhomboidea is designated as the lectotype of the species; however, P. rhomboidea is a synonym of P. mangula. In addition, KossmannRäuber's Pempheris erythraea and P. russellii Day, 1888 are also synonyms of P. mangula. Of two existing syntypes of P. nesogallica from Mauritius, one is designated as the lectotype, the other is re-identified as P. mangula; P. nesogallica is presently known only from the southern Red Sea. This species has a similar morphology to P. mangula, but can be distinguished by a smaller eye than P. mangula, and lack irregular faint longitudinal light stripes on the body side. Pempheris tominagai are distinguished from P. schwenkii Bleeker 1855, formerly misidentified, by the form of posterior nostril, scale counts, color of caudal fin, and by a 2.1% mitochondrial DNA sequence divergence.

The taxonomic status of Gerres longirostris (Lacepede, 1801), Gerres britannus (Lacepede, 1802), and Gerres poieti Cuvier, 1829, is examined. Gerres longirostris is considered a valid species and a senior synonym of G. britannus, G. poieti, and Gerres acinaces Bleeker, 1854a, and four other species (Gerres lineolatus Playfair, 1867, Gerres longicaudus Alleyne and Macleay, 1876, Gerres rueppellii Klunzinger, 1884, and Gerres darnleyense Ogilby, 1913). Gerres longirostris is redescribed, with designation of a neotype from Madagascar, Indian Ocean. Gerres oblongus Cuvier, 1830, is also confirmed as a valid species and a senior synonym of Gerres macrosoma Bleeker, 1854b, and Gerres gigas Gunther, 1862. A lectotype is designated for G. oblongus and a neotype for G. macrosoma. Gerres longirostris and G. oblongus belong to the ”Gerres longirostris complex.” Gerres longirostris differs from G. oblongus in having a deeper body (mean 39% SL vs mean 33% SL in G. oblongus), fewer pored lateral line scales (4...

The Australian marine atherinid fish, Atherinomorus vaigiensis (Quoy and Gaimard, 1825), having long been synonymized under A. lacunosus (Forster in Bloch and Schneider, 1801), is redescribed as a valid species based on the holotype and non-type specimens. Atherinomorus vaigiensis, known only from eastern and western Australia, differs from other congeners in lacking a distinct tubercle on the posterior end of the dentary and having the posterior tip of the upper jaw not extending beyond a vertical through the anterior margin of the pupil, 12–15 anal fin soft rays, 24–28 lower gill rakers, 39–42 midlateral scales, and a narrow midlateral band (width about 2/3 to 5/6 that of midlateral scale at level of anal fin origin). Atherina cylindrica Valenciennes in Cuvier and Valenciennes, 1835 and Pranesus ogilbyi Whitely, 1930 are regarded as junior synonyms of Atherinomorus vaigiensis.

A new shrimp-associated goby, Stonogobiops yasha sp. nov., is described on the basis of nine specimens collected from the Ryukyu Islands, Japan. This species is easily distinguished from other congeneric species in having reddish-orange stripes on a white body and only two median cephalic sensory pores on the head.

Taxonomic status of Gerres limbatus Cuvier in Cuvier and Valenciennes, 1830 and G. lucidus Cuvier in Cuvier and Valenciennes, 1830 was studied. The two species were reassessed as the same species, the latter corresponding to young of the former, on the basis of examination of their eight syntypes and other comparative specimens. Gerres limbatus clearly differs from other congeners in having 2½–3 (usually 2½) scales between the 5th dorsal fin spine base and the lateral line, and four or five diffuse, dark saddle patches mainly along the back in life (more apparent in small specimens less than ca. 65 mm in standard length, or preserved and stressed live specimens) (vs. usually more than 3½ scales between fifth dorsal fin spine base and lateral line, and and no such body color pattern of G. limbatus in other congeners). The species is currently known from the southern and western coasts of India including Sri Lanka, the Malay Peninsula, Gulf of Thailand, and Indonesia, becoming rare in occurrence eastward.

A new species, Polydactylus siamensis, is described on the basis of eight specimens from Thailand. The species is similar to P. plebeius (Broussonet, 1782) in having five pectoral filaments and several dark stripes along the scale rows above and below the lateral line, but differs from the latter in having lower counts of pectoral fin rays (15 vs. 16–18 in P. plebeius), pored lateral line scales (54–58 vs. 60–68), scale rows above and below the lateral line (7 and 10 or 11, respectively vs. 8 or 9 and 12 or 13, respectively) and gill rakers (9 or 10 upper series, 13 or 14 lower and 22–24 total vs. 9–14, 13–18 and 24–32, respectively), and a longer upper jaw (mean 17% [range 16–17%] of standard length vs. 15% [13–16%]). Polydactylus siamensis is currently known only from Bangkok and Songkhla, Gulf of Thailand, and Phuket Island, Andaman Sea, whereas P. plebeius is widely distributed in the Indo-Pacific.

The Indo-Pacific marine atherinid fishes, Atherinomorus endrachtensis (Quoy and Gaimard, 1825) and Atherinomorus duodecimalis (Valenciennes in Cuvier and Valenciennes, 1835), having long been confused with each other, are redescribed as valid species based on the types and nontype specimens collected from the eastern Indian Ocean and West Pacific. Atherinomorus endrachtensis, known from the Philippines, Palau, North Sulawesi and Maluku Is. (Indonesia), and New Guinea, differs from other congeners in lacking a tubercle on the dentary and having the posterior tip of the upper jaw not extending beyond a vertical through the anterior margin of the pupil, usually 10–11 anal fin soft rays, 33–35 midlateral scales, a narrow midlateral band (ca. half midlateral scale width at anal fin origin), and 3 distinct longitudinal broken black lines laterally and ventrolaterally on the body. A lectotype is designated for Atherina lineata Gunther, 1872, regarded as a junior synonym of Atherinomorus endrachtensis. Atherinomorus duodecimalis, known from Sri Lanka, Thailand, Yaeyama Is. (Japan), the Philippines, Indonesia, New Guinea, Queensland (Australia), and New Caledonia, differs from other congeners in having a tubercle on the posterior end of the dentary, the posterior tip of the upper jaw not extending beyond a vertical through the anterior margin of the pupil, usually 12–13 anal fin soft rays, 35–38 midlateral scales, and a narrow midlateral band (ca. 1/2 or 3/4 midlateral scale width at anal fin origin). Atherina balabacensis Seale, 1910 is regarded as a junior synonym of Atherinomorus duodecimalis.

Gerres silaceus n. sp. is described from the holotype and two paratypes from the southern Malay Peninsula. The species is included as the fourth species in the “G. setifer complex” [G. chrysops Iwatsuki, Kimura and Yoshino, G. decacanthus (Bleeker), G. setifer (Hamilton), G. silaceus n. sp.], differing from all other congeners from the Indo-Pacific in having two supraneural bones and small size (less than 100 mm in standard length vs three supraneural bones and adults > 100 mm SL). The new species is further characterized by presence of IX, 10 dorsal fin rays, 34 or 35 lateral line scales, 3.5 scales between the 5th dorsal fin spine base and lateral line, caudal fin short (mean 29% of SL), slender second anal fin spine, pelvic fin ray with a wide white margin posteriorly, and a uniformly silvery ocher body. Gerres silaceus differs from G. setifer and G. decacanthus in body color, the last dorsal fin spine slightly shorter or similar length to the penultimate spine, higher gillraker counts and bro...

A new shrimp-associated goby,Amblyeleotris melanocephala, is described on the basis of specimens from Okinoshima Island. Kochi Prefecture, and Okinawa Island, Okinawa Prefecture, Japan. The species is distinguished from other members of the genus by the following combination of characters: head dark brown, a few yellow spots on pectoral fin base and opercular margin, 13 second dorsal and 13 anal fin soft rays, 20 pectoral fin rays, longitudinal scales 92–101, proportional length of interpelvic connecting membrane relative to longest pelvic fin ray (CM-value) 0.46–0.55, presence of a ventral frenum, midline of nape naked, sides scaled above midpoint between preopercle and opercle.

Polydactylus macrochir (Gunther, 1867), for many years identified asP. sheridani (Macleay, 1884), is redescribed as valid and a senior synonym of the latter species, following examination of the holotype of the former and comparative material.Polydactylus macrochir is characterized by 14 or 15 pectoral-fin rays (usually 14), five pectoral filaments, 70–76 pored lateral-line scales, 32–35 gill rakers, occipital profile concave in adults, posterior margin of maxilla extending considerably beyond posterior margin of adipose eyelid, depth of posterior portion of maxilla greater than dermal eye opening in adults, second spine of first dorsal fin very strong and long pectoral-fin rays (22–27% of standard length).Polydactylus macrochir is currently known only from northern Australian and southern Papua New Guinea, being endemic to those areas.

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.

A new serranid fish,Liopropoma dorsoluteum sp. nov., is described on the basis of two specimens from Yaeyama Is., Okinawa, Japan. The new species is most similar toL. erythaeum Randall & Taylor, 1988, in having the following characters: Dorsal fin rays VIII, 12; anal fin rays III, 9; pored lateral line scales 52–53; anterior nostril situated midway between posterior nostril and anterior tip of snout; slightly forked caudal fin with both lobes rounded. It differs from the latter species in having a shorter pectoral fin (23.4–23.8% SL vs. 26.9–29.0% SL), greater preanus length (65.6–68.0% SL vs. 63.3–65.1% SL), fewer gill rakers (6+12 vs. 6–7+14–15) and yellow coloration on the back (vs. light red on head and body) in fresh specimens.

Gerres chrysops, a new gerreid species from the Gulf of Thailand, is described on the basis of 29 specimens, 58–83 mm in standard length (SL). A small-sized species (less than 100 mm SL), it is characterized by a silvery-gold sheen on the head and trunk, vivid yellow or yellowish-hyaline fins in life, two supraneural bones (formula 0/0/2/) and dorsal fin rays usually IX, 10. The new species is similar toG. decacanthus (Bleeker, 1865) andG. setifer (Hamilton, 1822), which are redescribed. being similarly small valid gerreid species characterized by two supraneural bones. Together, the three species comprise “theGerres setifer complex.”Gerres chrysops differs from bothG. decacanthus andG. setifer in life and fresh colors, the body being silvery-gold with vivid yellow or yellowish dorsal, caudal, anal and pelvic fins, and yellowish-hyaline pectoral fins (vs. silver body with hyaline fins in the latter two species).Gerres setifer differs fromG. chrysops andG. decacanthus in having the last dorsal fin spine longer than the penultimate spine (vs. almost same length or shorter), usually ten dorsal fin spines and nine soft dorsal rays (vs. usually IX, 10), and 8 or 9 lower series gill rakers (vs. usually 7).Gerres decacanthus differs fromG. chrysops andG. setifer in having a shorter head, lesser body depth at the first anal fin spine base, lesser body width at the pectoral fin base, and shorter second dorsal and third anal fin spines. The new species is currently known only from Angsilla, near Bangsaen, and around Si Chang Island, northeastern Gulf of Thailand.Gerres decacanthus inhabits southern Chinese waters andG. setifer is currently known from the Bay of Bengal to the Andaman Sea.

A taxonomic review of Japanese species of the creediid genusLimnichthys recognised the following:L. fasciatus, L. nitidus (a senior synonym ofL. donaldsoni) andL. orientalis sp. nov.L. fasciatus has an antitropical distribution.L. orientalis sp. nov. differs from its most similar congener,L. nitidus, in having fewer scales above and below the lateral line (2 vs. 3) and the fifth pelvic fin ray shorter or absent, and in the shape of cirri on the lower jaw.

A new fossil priacanthid fish,Cookeolus spinolacrymatus, is described on the basis of a single specimen from the Late Pliocene Shinzato Formation, Shimajiri Group, Miyagi-shima, Okinawa, Japan. This species is distinguished from the Recent speciesC. japonicus (Cuvier, 1828) by having a strong spine on the anterior portion of the lacrymal. The specimen was identified as a small benthic adult, or large juvenile, based on comparison with pelvic fin length development in the Recent species.

A new fossil serranid fish,Niphon macrocephalus, is described on the basis of a single specimen from the Late Pliocene Shinzato Formation, Shimajiri Group, Miyagi-shima, Okinawa, Japan. This species is distinguished from the Recent speciesNiphon spinosus Cuvier, 1828, in having the following four characters: (1) large head, (2) long frontals, (3) rounded posteroventral angle of maxilla, and (4) large 3rd hypural.

Gerres macracanthus Bleeker, 1854, for many years having been explicitly or tentatively synonymized withG. filamentosus Cuvier, 1829, is redescribed as a valid species.Gerres macracanthus differs fromG. filamentosus in lacking vertical rows of dark ovoid spots on the body, having instead only indistinct vertical bands in both subadult and adult stages, in addition to shorter second and third anal fin spines (9.1–13.9% and 10.4–14.4% of standard length [SL] vs. 12.3–19.6% and 11.9–17.3% of SL), fewer ored lateral line scales (41–44 vs. 43–46) and fewer scales between the base of the 5th dorsal fin spine and the lateral line (4–5 vs. 4 1/2–5 1/2), and above and below the lateral line (5 1/2–6 1/2/9 1/2–10 1/2 vs. 6 1/2–7 1/2/10 1/2–11 1/2). AlthoughG. filamentosus has similarly, indistinct vertical bands on the body up to ca. 100 mm SL, specimens over ca. 100 mm SL develop diffuse ovoid spots in each vertical band. Furthermore,G. macracanthus is generally a smaller species, apparently attaining a maximum size of ca. 170 mm SL, compared with ca. 250 mm SL forG. filamentosus. Formerly known from the Philippines, Indonesia, New guinea, India and the Arabian Gulf,G. macracanthus is newly-recorded from Japan, China, the Gulf of Thailand, the Red Sea and South Africa. A lectotype and three paralectotypes are designated forG. macracanthus Bleeker, 1854, in addition to a neotype forG. filamentosus Cuvier, 1829.

Two new shrimp-associated gobies,Amblyeleotris yanoi sp. nov. andA. masuii sp. nov. are described on the basis of specimens from Iriomote-jima Island and Okinawa-jima Islands, Okinawa Prefecture, Japan.A. yanoi is distinguished from other members of the genus by the combination of the following characters: 14 anal fin soft rays, 19 pectoral fin rays, 97–103 longitudinal scales, a candle flame-shaped marking on the caudal fin, a very low membrane connecting the pelvic fins and absence of a ventral frenum.A. masuii differs from all other congeners by having 92–97 longitudinal scales, the length of the interpelvic connecting membrane relative to the longest pelvic fin ray (0.43–0.66), black blotches on the sides of the chin, and blue spots on the opercle and preopercle.

The validity and authorship of Parapercis elongata are discussed. Although Fourmanoir (1967) has been considered to be the author of P. elongata , Fourmanoir (1965) satisfies the nomenclatural requirements associated with the availability of species names and P. elongata Fourmanoir, 1965 has priority over P. elongata of Fourmanoir, 1967. Although the holotype of P. elongata was not able to be conclusively determined, no significant differences were recognized between the original description of P. elongata and the holotype and non-types of Parapercis alboguttata (Gunther, 1872). Accordingly, P. elongata Fourmanoir, 1965 is determined to be a junior synonym of P. alboguttata .

Four species of the fish genus Pempheris are recognized for the Red Sea: P. adusta Bleeker, 1877; P. mangula Cuvier, 1829; P. nesogallica Cuvier in Cuvier & Valenciennes, 1831; and a new species P. tominagai . All are wide-ranging in the western Indian Ocean, and P. mangula has migrated via the Suez Canal to the eastern Mediterranean Sea. Morphological and genetic analysis of 15 species in this genus show that P. adusta , a widely distributed species, that can't be divided into different species, because of the continuity of morphologies and distribution, and lack of variance in genetics between Indian Ocean, Red Sea, and Pacific Ocean populations. This confirms that the two subspecies described by Randall et al . (2013) are both synonyms of P. adusta . Pempheris adusta is distinguished from other species by a blackish spot on pectoral fin base, pored lateral-line scales 56–64, scale rows above lateral line 4 1/2–6 1/2, distinct blackish band on outer edge of anal fin, and blackish band on posterior edge of caudal fin. Pempheris mangula was named by Cuvier (1829) in a footnote making reference to a drawing and short description in Russell (1803) of a Pempheris from southeast India, giving only the native name ''Mangula-Kutti'', and listing no specimen. The wide distribution of this species, from the Indian Ocean to the Red Sea is also demonstrated by morphological and genetic analysis. Thus, the specimen collected from southern India is herein designated as the neotype. This species is distinguished from other species by its huge eye, deep body, blackish tip of the dorsal fin, pored lateral-line scales 49–60, and scale rows above lateral line 4 1/2–5 1/2. The extant syntype of Kossmann & Rauber's P. rhomboidea is designated as the lectotype of the species; however, P. rhomboidea is a synonym of P. mangula . In addition, Kossmann & Rauber's Pempheris erythraea and P. russellii Day, 1888 are also synonyms of P. mangula . Of two existing syntypes of P. nesogallica from Mauritius, one is designated as the lectotype, the other is re-identified as P. mangula ; P. nesogallica is presently known only from the southern Red Sea. This species has a similar morphology to P. mangula , but can be distinguished by a smaller eye than P. mangula , and lack irregular faint longitudinal light stripes on the body side. Pempheris tominagai are distinguished from P. schwenkii Bleeker 1855, formerly misidentified, by the form of posterior nostril, scale counts, color of caudal fin, and by a 2.1% mitochondrial DNA sequence divergence.