Molecular evidence for the taxonomic status of three species of the <Emphasis Type="Italic">Sphyraena obtusata</Emphasis> group (Perciformes: Sphyraenidae) from East Asia

Genetic differences among the three species of Sphyraena with two gill rakers from East Asia (S. iburiensis, S. obtusata, and S. pinguis, defined recently as the S. obtusata group), were investigated using 799-bp sequences of the mitochondrial cytochrome b gene. Pairwise sequence differences within each of the three species were 0.0–0.4% (S. iburiensis), 0.0–0.4% (S. obtusata), and 0.0–0.6% (S. pinguis), respectively, pairwise sequence differences among the three species being 18.3–18.6% (S. iburiensis vs. S. obtusata), 14.9–15.4% (S. iburiensis vs. S. pinguis), and 17.6–18.3% (S. obtusata vs. S. pinguis), respectively. The extent of the latter were comparable to those among four other congeneric species, S. africana, S. forsteri, S. helleri, and S. japonica (16.0–24.5%). Phylogenetic analysis using the maximum-likelihood method indicated reciprocal monophyly of the three species, each clade being supported by a bootstrap value of 100%. These findings fully supported the taxonomic status of these species, recently elucidated by detailed morphological comparisons. In addition, the S. obtusata group formed a strongly supported clade against the four other congeneric species.     

Revision of the East Asian genus <Emphasis Type="Italic">Ditrema</Emphasis> (Embiotocidae), with description of a new subspecies

A review of the species and subspecies of Ditrema from East Asia recognized the following taxa: D. jordani Franz, 1910, D. temminckii pacificum subsp. nov., D. t. temminckii Bleeker, 1853, and D. viride Oshima, 1940. Ditrema jordani is characterized by a coppery-red body when fresh, the posterior end of the dorsal-fin base anterior to that of the anal-fin base, a dark rounded marking on the anterior suborbital area margined with white lines or a broad dark inverse trapezoid marking on the anterior part of the suborbital region, the lower half of the spinous portion of the dorsal fin often with a longitudinal black stripe, and a faint longitudinal dark line along the anal-fin base. Ditrema temminckii is characterized by a silvery body, usually bluish dorsally when fresh, a black oblique band on the anterior suborbital area, the spinous portion of the dorsal fin with a black distal margin, and no dark line along the anal-fin base. Ditrema t. pacificum, mainly distributed along the Pacific Ocean coast, differs from D. t. temminckii, mainly distributed along the coast of Sea of Japan, in lacking a dark spot on the anterior portion of the preopercle (vs. dark spot present in the latter), but having a black line along the posterior margin of the pelvic-fin spine (vs. black spot anteriorly on base of pelvic fin), fewer dorsal-fin spines (usually 9 or 10 vs. 10 or 11), more dorsal-fin soft rays (mode 21 vs. mode 20), and longer pectoral, pelvic, and caudal fins. The two nominal species (D. smitti and D. leave) are regarded as junior synonyms of D. t. temminckii. Ditrema viride is characterized by a silvery, dorsally yellowish-green body when fresh, 9–11 dorsal-fin spines (mode 10), a dark triangular marking on the anterior suborbital area, the spinous portion of the dorsal fin with a black distal margin, a longitudinal black line along the anal-fin base and the pelvic fin slightly darkish, and lacking a black spot anteriorly on the base. Neotypes are designated for D. jordani and D. viride. A key to the species and subspecies of Ditrema is provided.     

<Emphasis Type="Italic">Vanderhorstia papilio</Emphasis>, a new shrimp-associated goby from the Ryukyu Islands,Japan (Perciformes: Gobiidae: Gobiinae), with comments on the limits of the genus

A new gobiid fish, Vanderhorstia papilio, is described based on a single specimen (40.9mm SL) captured from a sandy-mud bottom at a depth of 45m in a protected bay of Iriomote-jima Island, Ryukyu Islands, Japan. It is distinguished from congeners in having the following combination of characters: 11 segmented dorsal-fin rays; 11 segmented anal-fin rays; 27 longitudinal scales; 11 predorsal scales; third spine of first dorsal fin elongate, filamentous, and longer than preceding spine; fifth and ninth branched caudal-fin rays elongate, filamentous, and forming bifurcated caudal fin; fifth and ninth branched caudal-fin rays with a single branch in each; cephalic sensory-papillae row a comprises three widely-spaced papillae; when live or fresh, numerous small yellow spots scattered on head, body, and dorsal fins; dusky yellowish-brown vertical bar below eye; four dark gray-brown saddles on body, in addition to a similarly colored large blotch at midlateral caudal-fin base. The limits and diagnosis of the genus Vanderhorstia are discussed.     

The Saurida undosquamis group (Aulopiformes: Synodontidae), with description of a new species from southern Japan

Four lizardfishes of Saurida (family Synodontidae), S. undosquamis, S. umeyoshii sp. nov., S. macrolepis, and S. longimanus, are described. All are recognized here as the Saurida undosquamis group, characterized by having dark dots on the upper margin of the caudal fin, pectoral fin exceeding origin to pelvic fin, anterior rays of dorsal fin neither elongate nor filamentous, predorsal length greater than distance between dorsal-fin and adipose-fin origins, 46–55 pored lateral-line scales, and vomer with 0–8 teeth. Saurida undosquamis, from northern West India and West Pacific, excluding East Asia, differs from others in having lateral-line scales ridged on the caudal peduncle, conspicuously concave posterior margin of the pectoral fin, 51–55 pored lateral-line scales, and 50–53 vertebrae. Saurida umeyoshii sp. nov., from southern Japan and the East China Sea, is defined by three rows of indistinct dark blotches on, above, and below the lateral line, distribution of scale pockets with melanophores on their posterior part extending over the entire abdominal region from the lateral line in specimens over ca. 130 mm SL, lateral-line scales not ridged on caudal peduncle, 49–52 pored lateral-line scales, and 48–50 vertebrae. Saurida macrolepis, from the Indo-West Pacific, is characterized by 46–49 pored lateral-line scales and 45–48 vertebrae. Saurida longimanus, from northern West India, northwest Australia, and southern Indonesia, differs from the others in having a long pectoral fin extending past the origin of the dorsal fin. Some geographic variations are found in S. macrolepis. Saurida grandisquamis is confirmed as a junior synonym of S. undosquamis, based on examination of the type specimens. A key to species in the S. undosquamis group is included.     

Larval development of two species of barracuda,Sphyraena guachancho andS. tome (Teleostei: Sphyraenidae), from southeastern Brazil

Morphological development of barracudas (Sphyraena guachancho andS. tome) is described, based on larval and juvenile specimens collected in the southeast Brazilian Bight. Preflexion larvae of the two species are similar, butS. tome larvae can be distinguished from those ofS. guachancho by having small melanophores on the midbrain and a row of melanophores along the ventral midline of the lower jaw and isthmus. Flexion and postflexion larvae ofS. tome are more slender than those ofS. guachancho. Morphology and pigment patterns ofS. tome are similar to those ofS. borealis from the north Atlantic. whereasS. guachancho larvae are similar toS. barracuda in having a fusiform body, advanced position of the pelvic fins and a heavily pigmented tail region, but differ in having a fleshy tip on the lower jaw in postflexion and juvenile stages.     

Lycodes nishimurai, a new deep-sea eelpout (Teleostei: Zoarcidae) from the Sea of Japan

A new zoarcid fish, Lycodes nishimuari, is described on the basis of four specimens from the Yamato Bank, the Sea of Japan, at depths of 642–669 m. Although this species resembles Lycodes diapterus, L. hubbsi, L. pectoralis, L. macrochir, and L. nakamurae in having a deep notch in the pectoral fin and a single lateral line on the body, it is distinguished from them by the following combination of characters: no scales on pectoral fin base; scales on dorsum before dorsal fin origin; suborbital, preopercular, and last postorbital pores with risen rim; whitish lips; no whitish transverse bars on body; pectoral fin membrane and anterior part of dorsal fin membrane without black spots; basal color of vertical fins black. Supplementary material to this paper is available in electronic format at .     

Thysanophrys papillaris, a new species of flathead from the Andaman Sea and Northern Australia (Scorpaeniformes: Platycephalidae)

A new platycephalid,Thysanophrys papillaris, is described on the basis of six specimens (78–121 mm SL) collected from the Andaman Sea and off northern Australia (Timor and Arafura Seas). This new species can be distinguished from other congeners by the following combination of characters: presence of a single short papilla on upper surface of eye, longer snout, smaller body scales. 11 second dorsal-fin rays and 12 anal-fin rays, presence of four or more suborbital spines usually, branched short iris lappet, ctenoid lateral-line scales and interopercle not extended posteroventrally.     

<Emphasis Type="Italic">Sebastapistes taeniophrys</Emphasis> (Fowler 1943): a valid scorpionfish (Scorpaenidae) from the Philippines

The poorly known scorpionfish, Scorpaena taeniophrys, originally described from two specimens from the Philippines, is redescribed as a valid species of Sebastapistes. Sebastapistes taeniophrys differs from all other congeners in having a combination of 15 pectoral-fin rays, 31–33 scale rows in longitudinal series, 11–14 pored lateral-line scales, 3 predorsal scale rows, 12 gill rakers, 3 suborbital spines, absence of coronal spines, lower opercular spine with a median ridge and not covered with scales, ctenoid body scales, several dark transverse bands on ventral surface of mandible, a distinct elongate black blotch distally between the second or third and seventh dorsal-fin spines, and no black blotch on the nape.     

Redescriptions of the Indo-Pacific atherinid fishes <Emphasis Type="Italic">Atherinomorus forskalii</Emphasis>, <Emphasis Type="Italic">Atherinomorus lacunosus</Emphasis>, and <Emphasis Type="Italic">Atherinomorus pinguis</Emphasis>

The Indo-Pacific marine atherinid fishes Atherinomorus forskalii (Rüppell, 1838), Atherinomorus lacunosus (Forster, 1801), and Atherinomorus pinguis (Lacepède, 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. Supplementary material to this paper is available in electronic format at     

广西云南鳅属鱼类一新种记述

2003年5月,在广西壮族自治区都安县高岭乡红水河水系采集到一批条鳅标本。经鉴定,为云南鳅属(Yunnanilius)一未经发表的新种。新种长须云南鳅(Yunnanilus longibarbatus sp.nov.)属于黑斑云南鳅种组(Yunnanilus nigromaculatusgroup),并与黑斑云南鳅[Y.nigromaculatus(Regan)]、钝吻云南鳅(Y.obtusirostris Yang)、长背云南鳅(Y.longidorsalisLi,Tao et Lu)和巴江云南鳅(Y.bajingensisLi)等4种最为相似。长背云南鳅背鳍分枝鳍条11根,颌须短,仅达眼中部,背鳍起点距吻端较距尾鳍基为近,可与包括本种在内的其余4种相区别(背鳍分枝鳍条8-9根,颌须达到或超过眼后缘,背鳍起点距吻端较距尾鳍基为远)。本种和钝吻云南鳅上颌中央无齿状突、下颌中央无缺刻,可与黑斑云南鳅和巴江云南鳅相区别。本种在鳍条数、上下颌、背鳍起点的位置、尾鳍形状、鳞片、头部侧线管孔、体侧纵纹等方面与钝吻云南鳅最为相似,但本种可藉多个特征与后者相区别:颌须伸过眼后缘至鳃盖后缘的中点至鳃盖后缘,是已知云南鳅中须最长的;背鳍不分枝鳍条下1/3处具一不显著黑色斑点(vs.无斑);体侧纵纹,其宽窄于眼径,较大个体背鳍之前的纵纹被虫状纹取代(vs.体侧纵纹始终存在,其宽约等于眼径);头背具斑点(vs.无斑);尾柄较细长,体长/尾柄长=5.3-6.1(vs.7.4-9.0,尾柄长/尾柄高=1.3-1.8vs.0.8-1.1)。     

Gerres methueni Regan, 1920, a senior synonym ofG. rappi (Barnard, 1927) (Perciformes: Gerreidae)

Gerres methueni Regan, 1920, for many years identified asG. rappi (Barnard, 1927), is redescribed as a senior synonym of the latter species, following examination of two syntypes of the former and comparative material from South Africa and Madagascar.Gerres methueni is characterized by prominent dark stripes along the scale rows above the lateral line and the 4 or 5 rows immediately below it, 5–17 small scales on the preopercular flange, arranged in 1–3 scale row(s) at the corner, 42–44 pored lateral line scales+3–5 additional pored scales on the scaly sheath of the caudal fin base, 41/2–51/2 scales between the fifth dorsal fin spine base and lateral line, and second dorsal fin spine length equal to or slightly shorter than the third dorsal fin spine length.Gerres methueni is currently known from South Africa, southern Mozambique and Madagascar, being endemic in those areas.     

Validity of <Emphasis Type="Italic">Abudefduf caudobimaculatus</Emphasis> Okada and Ikeda 1939 and synonymies of <Emphasis Type="Italic">Abudefduf vaigiensis</Emphasis> (Quoy and Gaimard 1825) (Perciformes: Pomacentridae)

Abudefduf caudobimaculatus Okada and Ikeda 1939, having long been regarded as a junior synonym of Abudefduf vaigiensis (Quoy and Gaimard 1825), is herein redescribed as a valid species on the basis of the holotype and 77 additional specimens. Abudefduf caudobimaculatus can be distinguished from A. vaigiensis in having 11–13 (modally 12) dorsal-fin soft rays, 4 scale rows above the lateral line, 2½ scale rows between the middle of the spinous portion of the dorsal-fin base and lateral line, 3–4 (4) scale rows on the cheek, scales always present on the anteroventral region of the head, eleventh and last dorsal-fin spines and pectoral-fin length 15.5–18.4%, 17.1–20.6%, and 33.5–39.9% of SL, respectively, two black spots on the caudal-fin base, anteriormost bar descending to behind the pectoral-fin base, 0–1 tubed lateral-line scales on the fourth vertical bar, and third to seventh (usually fifth or sixth) dorsal-fin soft ray base at the anterior margin of the fourth vertical bar. Synonymies of A. vaigiensis are discussed with designations of lectotypes for Glyphisodon vaigiensis and Glyphisodon rahti.     

中国广西盲鳅一新种——环江高原鳅(英文)

2007年4月,在广西壮族自治区环江县川山镇乐衣村附近一洞穴采集到一批盲鳅类标本。经鉴定,为高原鳅属(Triplophysa)鱼类一新种,被命名为环江高原鳅(Triplophysa huangjiangensis)。该新种以以下组合特征与高原鳅属的其他已知种类相区别:无眼;通体无鳞;尾鳍分叉;尾柄上、下叶具发达的软鳍褶;背鳍后缘平截;背鳍起点距尾鳍基的距离短于距吻端的距离;背鳍分枝鳍条数为8~9;胸鳍分枝鳍条数为10~11;腹鳍分枝鳍条数为6~7;臀鳍分枝鳍条数为6;尾鳍分枝数为13~14;胸鳍长为胸鳍起点至腹鳍起点间距的52.3%~70.7%;腹鳍起点位于背鳍起点之前下方;外侧吻须最长,为侧面头长的47.0%~73.8%;前鼻孔位于一短管中,末端延长呈须状;鳔后室发达,末端可伸达腹鳍起点。     

The <Emphasis Type="Italic">Leiognathus aureus</Emphasis> complex (Perciformes: Leiognathidae) with the description of a new species

Taxonomic analysis of a group of morphologically similar ponyfishes (Perciformes: Leiognathidae) establishes a complex comprising three valid species: Leiognathus aureus Abe and Haneda, 1972, widely distributed in the western Pacific Ocean (Taiwan, Philippines, Thailand, Singapore, Indonesia, and northern Australia); L. hataii Abe and Haneda, 1972, currently known only from Ambon, Indonesia; and L. panayensis sp. nov. Kimura and Dunlap, currently known only from Panay Island, the Philippines. The L. aureus complex can be defined by the following combination of characters: mouth protruding forward, not downward; small but sharp conical teeth uniserially on jaws; a black line between lower margin of eye and lower jaw articulation; and lateral line incomplete, ending below posterior part of dorsal fin base or on anterior caudal peduncle. Leiognathus hataii differs from both L. aureus and L. panayensis in having a large dark blotch below the spinous dorsal fin base and fewer counts of scales (lateral line scales 50–58 vs. 64–85 in the latter two species; scales above lateral line 7–10 vs. 12–18; scales below lateral line 22–26 vs. 30–41). Leiognathus panayensis is distinguished from L. aureus in having a deeper body (41–51% SL vs. 35–45% SL in the latter), long posterior limb of maxilla (21–25% HL vs. 15–23% HL), wholly scaled belly (vs. naked along preanal median keel), and a dark blotch on nape (vs. absent).     

<Emphasis Type="Italic">Rainfordia opercularis</Emphasis>, a liopropomin serranid (Teleostei: Serranidae: Epinephelinae): corroborative evidence from settlement-stage larvae

Rainfordia opercularis was described in 1923 from a single specimen taken in Edgecumbe Bay, Queensland, Australia. The species is rare in museum collections, and the larvae have not been described. In 1999, two settlement-stage larvae (20–21 mm in standard length) were collected in light traps set off Lizard Island, Great Barrier Reef, Queensland. The smaller of the two has one thin, flexible, extremely elongate dorsal-fin spine encased in a pigmented sheath. The larger specimen lacks an elongate dorsal-fin spine and exhibits caudal-fin pigment characteristic of adults. A combination of features in one or both of the settlement-stage larvae support the placement of Rainfordia in the epinepheline-serranid tribe Liopropomini: presence of an elongate, filamentous dorsal-fin spine serially associated with the first dorsal-fin pterygiophore; presence of a spine on the inner preopercular ridge; presence of dense pigment on the frontals; absence of an elongate spine at the angle of the preopercle; and absence of supraorbital spination. Supplementary material to this paper is available in electronic format at     

Owstonia kamoharai (Perciformes: Cepolidae), a new bandfish from Japan

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.     

Corydoras fulleri (Siluriformes: Callichthyidae), a new catfish species from the rio Madeira basin,Peru

A new long-snouted Corydoras species is described from two tributaries of the río Manuripe and a tributary of the río Madre de Dios, rio Madeira basin, Peru. Corydoras fulleri can be distinguished from its congeners by having the following features: (a) branch of the temporal sensory canal at sphenotic, which gives rise to the supraorbital canal, with two pores; (b) upper tooth plate of branchial arch with three series of teeth; (c) area at the corner of the mouth, ventral to the maxillary barbel, with a small fleshy flap; (d) two moderate-sized dark-brown or black blotches on caudal-fin base, one on its lateral portion and another one on its dorsal portion, blotches variably diffuse and/or fused with each other; (e) absence of a dark-brown or black stripe transversally crossing the orbit; (f) a longitudinal dark-brown or black stripe on the postdorsal region of flank midline, variably fused with the lateral peduncular blotch, some specimens with slender, longitudinally elongated, dark-brown or black blotch on flank midline, forming a dash-like marking, stripe or dash-like blotch diffuse in some specimens; and (g) region around dorsal-fin origin generally lacking dark brown or black blotch, or displaying diffuse blotch.     

Triplophysa ferganaensis,a new loach species from Fergana Valley in Central Asia (Teleostei: Nemacheilidae)

Triplophysa ferganaensis sp. nov. is described from the Shakhimardan stream, a small tributary of the Syr Darya, which does not reach the river in Fergana Valley. It can be distinguished from other valid Triplophysa loaches based on the following combination of characters: body smooth and scaleless, lateral line complete, posterior chamber of air bladder degenerated, inner gill rakers 10–11 on the first-gill arch, outer gill rakers absent, vertebrae 4 + 35–36, 8 + 8 branched caudal-fin rays, caudal peduncle depth 2.1–2.7 times its length, two supratemporal pores, dorsal-fin origin closer to the caudal-fin base than to the snout tip, caudal fin emarginated and pelvic-fin tip reaching the anus. The new species can also be distinguished from its congeners based on the molecular analyses of mitochondrial cytochrome oxidase subunit I (coI) gene sequences. The phylogenetic position of this new species indicates that it is a sister taxon of Triplophysa tenuis.     

Validity of the leiognathid fish,Gazza dentex (Valenciennes in Cuvier and Valencinnes, 1835), with designation of a lectotype, and redescription ofG. minuta (Bloch, 1795)

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.     

First record of the sea anemone Diadumene lineata (Verrill 1871) associated to Spartina alterniflora roots and stems, in marshes at the Bahia Blanca estuary, Argentina

We report the occurrence of the orange-striped green anemone Diadumene lineata (Verrill 1871) (=Haliplanella lineata) in salt marshes at the Bahía Blanca Estuary for the first time in August 2005. We also found this species attached to roots and stems of Spartina alterniflora, an association that has never been registered before. After their determination, sampling was performed during a year to evaluate seasonal abundance of this sea anemone. Results showed that D. lineata was present through the whole year, indicating the existence of a stable population. All individuals sampled were found attached to roots or stems of S. alterniflora, with the higher abundances detected in summer. Further studies are necessary to precise the potential effects of this exotic sea anemone on salt marsh communities.