Description of a new catfish, Silurus tomodai (Siluriformes: Siluridae) from central Japan

Zootaxa ◽  
2018 ◽  
Vol 4459 (3) ◽  
pp. 507
Author(s):  
YUSUKE HIBINO ◽  
RYOICHI TABATA

A new catfish, Silurus tomodai, is described based on 37 specimens; 132-514 mm > 139-514 mm [132–514 mm standard length (SL)] collected from streams of Mie, Aichi, Gifu, Shizuoka and Nagano prefectures of central Honshu Island, Japan. Although S. tomodai is closely related to S. lithophilus (Tomoda, 1961) based on partial mitochondrial DNA sequences, the former can be distinguished from the latter by the position of dorsal fin (predorsal-fin length 28.5–32.1% vs. 30.1–33.7% SL), a shorter head (18.5–21.2% vs. 19.5–22.2% SL) that is more broadly rounded in ventral view, a more slender body (depth at 10th anal-fin ray 12.9–18.3% vs. 15.7–18.8% SL, and 86.8–100.3% vs. 97.2–109.7% of body depth at anal-fin origin), longer mandibular barbel [20.4–47.7% vs. 10.7–35.3% of head length (HL)], shorter anal-fin rays (10th anal-fin ray length 32.2–38.3% vs. 37.3–45.3% HL), eye slightly protruding laterally beyond profile in dorsal view, and the shape of medial depression on anterior face of mesethmoid (deep and narrow vs. shallow and wide). Silurus tomodai differs from S. asotus, a species widely distributed in Japan including central Honshu Island, in the shape of vomerine-tooth band (typically separated into two distinct lenticular patches vs. continuous), the shape and size of teeth (small and slightly recurved vs. relatively large and recurved), snout length (34.7–38.9% vs. 33.0–36.5% HL), the length of lower jaw (110–124% vs. 124–138% of snout length), interorbital width (53.0–61.3% vs. 46.3–52.8% HL), eye location (vertical through anterior margin of pupil usually posterior vs. anterior terminus of lips), inter-mandibular barbel width (24.7–32.5% vs. 21.7–26.7% HL), vertebral count (62–65 vs. 58–63), pigmentation on underside of head (usually mottled with dark pigmentation vs. uniformly white, rarely dark with pale band along posteroventral margin of lower jaw) and eggs yellow (vs. light green). 

2019 ◽  
Vol 2019 ◽  
pp. 1-8 ◽  
Author(s):  
Renan Rodrigues Rocha ◽  
Rosana de Mesquita Alves ◽  
Rubens Pasa ◽  
Karine Frehner Kavalco

The Astyanax scabripinnis complex is composed of a large number of almost morphological indistinguishable species, including Astyanax paranae and Astyanax rivularis, which exist in the Paraná and São Francisco Basins, respectively, and sometimes are considered subspecies of the A. scabripinnis group or even are cited just as A. scabripinnis. The two river basins are separated by the Upper Paranaíba Arc, likely the main cause of the isolation of these species. We used geometric morphometric tools and DNA analyses of populations of both species to identify the differences between them. Geometric morphometrics separated the two species into distinct groups, whose main difference was the body depth. This is generally related to the speed of the water flow in the river basins. The maximum likelihood phylogram based on mitochondrial DNA sequences formed two main clades: one composed of the population of A. rivularis and the other, of A. paranae. In the haplotype network, the species were similarly separated into two groups from the same ancestral haplotype, with A. rivularis dispersing into two lineages in the São Francisco River Basin. The distribution of A. paranae is a consequence of a secondary dispersion event in the Paraná River Basin. It forms two lineages from a haplotype derived from the ancestor. The vicariant effect of separate basins, through the elevation of the Upper Paranaíba Arc, led to the allopatric speciation of the populations originating the present species. The results of geometric morphometrics and molecular data of the fish show the importance of this geological event in the biogeography and evolutionary history of the ichthyofauna of the region and indicate that the isolation of these species seems to be effective.


Zootaxa ◽  
2021 ◽  
Vol 4905 (1) ◽  
pp. 1-104
Author(s):  
THOMAS A. MUNROE

The flatfish genus Peltorhamphus Günther, 1862 (Pleuronectiformes: Rhombosoleidae) and its constituent species are redescribed based on examination of 1885 specimens. Four species are considered valid: three previously described (P. novaezeelandiae Günther, 1862, P. latus James, 1972, and P. tenuis James, 1972) and P. kryptostomus n. sp., described herein. Peltorhamphus novaezeelandiae, P. latus, and P. tenuis have widespread distributions on soft sediments in shallow coastal and inner continental shelf waters off both islands of New Zealand. Peltorhamphus novaezeelandiae has also been reported at the Chatham Islands. Previous reports of P. novaezeelandiae from Norfolk Island are erroneous. Peltorhamphus kryptostomus n. sp. has the most restricted geographic distribution in shallow coastal waters of the Otago-Southland region along the southeastern coast of South Island. The four species of Peltorhamphus are morphologically similar and overlap in many traditional meristic and morphometric features rendering identifications difficult, especially of juveniles and earlier life-history stages. Furthermore, throughout New Zealand waters, as many as three of the species possibly occur sympatrically, while in inshore areas of southeastern South Island, all four species may occur in sympatry. Novel morphological characters discovered in this study, combined with traditional diagnostic characters were used to identify and diagnose the species. Peltorhamphus tenuis is the most distinctive of the four, differing from congeners in the following combination of characters: greater length of second ocular-side pectoral-fin ray; its higher numbers of dorsal- and anal-fin rays and total vertebrae; having a series of small scales (best developed in specimens >70 mm SL) on blind sides of dorsal- and anal-fin rays (scales absent in congeners); its elongate body; and ocular-side pigmentation. The other three species are more similar morphologically and have frequently been misidentified both in fish collections and in some previous literature on these fishes. Of these three, P. novaezeelandiae, the largest in the genus, is distinguished from congeners by the combination of: its large size (reaching 510 mm SL vs. ≤ 200 mm SL); rounded head shape; blind-side squamation; the second ocular-side pectoral-fin ray shorter than body depth; ontogenetic variation in interorbital width; greater distance (4–8 scales wide) between ventral margin of lower eye and dorsal (upper) margin of rostral hood above the mouth; and 2–6 fleshy, finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Peltorhamphus latus differs from congeners by the combination of: its short (maximum 150 mm SL), relatively deep body and bluntly pointed snout; blind-side squamation; relatively long, robust gillrakers on first gill arch, with upper limb gillrakers long, but not usually overlapping tips of dorsalmost gillrakers on the lower limb; black pigment on entire roof of mouth; relatively large eyes and narrow interorbital width (without significant ontogenetic variation); short diagonal distance (usually 2–3 scales wide) between ventral margin of lower eye and dorsal (upper) margin of rostral hood above the mouth; and absence of finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Peltorhamphus kryptostomus n. sp. is distinguished from congeners by the combination of: its deep body and smoothly rounded snout; blind-side squamation; long, robust gillrakers on the first gill arch, with some posterior gillrakers on the upper limb overlapping tips of the first and second dorsalmost gillrakers on the lower limb; black pigment on the entire roof of the mouth; relatively large eyes and relatively narrow interorbital width; wide distance between ventral margin of lower eye and upper margin of rostral hood (3–6, usually 4–5, scales wide); and 1–4 finger-like filaments on the inner anteroventral margin of the fleshy skinfold on the ocular-side lower jaw. Ecological and life-history information are summarized for each species, and a key to juveniles > 40 mm SL and adults is also provided. Re-assessment of the number of valid species of Peltorhamphus provides better understanding of species diversity within this genus and within the Rhombosoleidae, as well as that for the flatfish assemblage residing in New Zealand waters. 


2018 ◽  
Vol 82 (3) ◽  
pp. 169
Author(s):  
Ronald Fricke ◽  
Daniel Golani ◽  
Brenda Appelbaum-Golani ◽  
Uwe Zajonz

The scorpionfish Scorpaena decemradiata n. sp. is described from off the coast of Israel in the Gulf of Aqaba, northern Red Sea. The new species is similar to S. porcus Linnaeus, 1758, but is characterized by dorsal fin spines XII, soft dorsal fin rays 10 (the last divided at base); pectoral fin rays 16, uppermost branched pectoral fin ray is the second; lacrimal with 2 spines over maxilla that point at nearly right angle from each other, the posterior pointing ventrally and slightly anteriorly; occipital pit well developed; anteriormost mandibular lateral-line pores small, separated; scales ctenoid; 59-62 scale rows in longitudinal series; scales absent on chest and pectoral fin base; and cirri developed over entire head and body, but no cirri on lower jaw. An updated checklist of the species of the genus Scorpaena Linnaeus, 1758 and a key to the species of the eastern Atlantic, Mediterranean Sea and Red Sea are presented.


Zootaxa ◽  
2021 ◽  
Vol 4996 (2) ◽  
pp. 322-330
Author(s):  
HEOK HEE NG ◽  
MAURICE KOTTELAT

Pseudobagarius eustictus, new species, is described from the Nam Heung drainage (a tributary of the Mekong River) in northern Laos. It is distinguished from congeners in having a unique combination of the following characters: a weakly-produced snout in which the upper jaw extends only slightly beyond the margin of the lower jaw when viewed ventrally, 3 tubercles on the posterior margin of the pectoral spine, eye diameter 8% HL, head width 24.1% SL, dark yellow dorsal and lateral surfaces of the head, pectoral spine lacking elongate extensions, pectoral fin reaching the pelvic-fin base when adpressed against the body, dorsolateral surfaces of body without longitudinal series of prominent tubercles, body depth at anus 13.7% SL, length of adipose-fin base 17.7% SL, caudal-peduncle depth 7.0% SL, and 33 vertebrae.  


Zootaxa ◽  
2020 ◽  
Vol 4762 (1) ◽  
pp. 1-66
Author(s):  
SHUMPEI KAWARADA ◽  
HISASHI IMAMURA ◽  
YOJI NARIMATSU ◽  
GENTO SHINOHARA

Eelpout species of the genus Lycenchelys Gill, 1884 recorded from Japanese waters are taxonomically revised. This study recognizes the following 11 species from Japanese waters as valid: Lycenchelys albomaculata Toyoshima, 1983, Lycenchelys aurantiaca Shinohara & Matsuura, 1998, Lycenchelys hippopotamus Schmidt, 1950, Lycenchelys maculata Toyoshima, 1985, Lycenchelys makushok Fedorov & Andriashev, 1993, Lycenchelys melanostomias Toyoshima, 1983, Lycenchelys rassi Andriashev, 1955, Lycenchelys remissaria Fedorov, 1995, Lycenchelys ryukyuensis Shinohara & Anderson, 2007, Lycenchelys squamosa Toyoshima, 1983 and Lycenchelys tohokuensis Anderson & Imamura, 2002. We redescribe species in detail based on type specimens as well as additional specimens in many cases. The synonymy of Lycenchelys brevimaxillaris Toyoshima, 1985 with L. melanostomias is supported in this study. Sexual dimorphism and changes with growth are revealed in L. albomaculata, L. aurantiaca, L. hippopotamus, L. makushok, L. melanostomias and L. rassi, all based on 10 or more specimens, for relative head length, head width, and upper and lower jaw lengths. In addition, we also found that the sizes at which sexual dimorphism can be recognized, and the tendencies for change with growth, differ among species. Furthermore, the dimorphism in head length is influenced by the snout length, eye diameter and/or postorbital length in L. albomaculata and L. aurantiaca. 


Zootaxa ◽  
2019 ◽  
Vol 4674 (3) ◽  
pp. 329-348 ◽  
Author(s):  
JEFFREY W. JOHNSON ◽  
JESSICA WORTHINGTON WILMER

A new species of epinephelid fish from northeastern Australia is described based on five specimens 408–564 mm SL collected by deep water demersal dropline fishing. Epinephelus fuscomarginatus sp. nov. is known from the Capricorn Channel, off the southern end of the Swain Reefs, Qld, Australia, in depths of 220–230 m. It is distinguished by a combination of dorsal-fin rays XI, 14, pectoral-fin rays 17, anal-fin rays III, 8, caudal-fin rounded, lateral-line scales 60–67, gill rakers 9–10 + 16–19 = 25–28, body depth 3.0–3.4 in SL, angle of preopercle broadly rounded, bearing 4–9 small non-prominent serrae, midlateral part of lower jaw with 2 rows of teeth, tooth patches on vomer and palatines narrow, in 2–3 and 2–4 rows, respectively, and coloration including broad dark brown margins to the soft dorsal, anal and caudal fins. There are no dark spots on the head, body, or fins at any known size and in subadults there are two faint pale brown bars radiating from the eye to the posterior margin of the opercle, and diffuse irregular brown wavy bars and blotches on the sides of the body. Comparison of the mitochondrial cytochrome c oxidase subunit 1 (CO 1) genetic marker utilised in DNA barcoding produced modest but consistent genetic divergences of 1.10% and 2.70 % between E. fuscomarginatus sp. nov. and its closest sampled congeners, E. magniscuttis and E. epistictus, respectively. Further evidence is presented to indicate that populations of E. epistictus currently recognised from the Indian Ocean east to the Indo-Australian Archipelago may be distinct from those from the Sea of Japan to the East China Sea. 


Zootaxa ◽  
2018 ◽  
Vol 4531 (1) ◽  
pp. 95
Author(s):  
HARALD AHNELT ◽  
MICHAEL SAUBERER

Schindleria macrodentata sp. nov., a new species of the paedomorphic gobiid fish genus Schindleria, is described from the Malay Archipelago. The two specimens were collected in 1929 during the “Dana Expedition” in the Molucca Sea between Sulawesi and Halmahera islands (00°29′N, 125°54′E) (Indonesia) and in the Sulu Sea close to Panay Island (11°43’N, 121°43′E) (Philippines). The new species is characterized by a slender body (body depth at pectoral fin base 3.6–3.7 % of SL and at anal fin origin 3.9–4.8 % of SL), a long second dorsal fin (first dorsal fin absent) originating distinctly anterior to the origin of the anal fin (predorsal length 61.8–65.2 % of SL and preanal length 71.7–75.8 % of SL), a short tail (from anus to tip of longest caudal fin ray) (22.1 % of SL), 19–20 dorsal fin rays and 10 anal fin rays, first anal fin ray below 9th dorsal fin ray, few large, widely spaced teeth in the upper and the lower jaws (7 on the premaxilla and 6 on the dentary), an elongated pectoral radial plate (length 3.7–4.5 % of SL) and, in the caudal skeleton, a procurrent ray with an additional spiny process at its base. No distinct urogenital papilla and no pigmentation on body are developed. In this study we present three morphological traits until now not considered as diagnostic characters for Schindleria, the shape of the pectoral radial plate, the shape of the last procurrent caudal spine and the shape of the arch formed by the lower jaw. We also discuss the caudal-fin skeleton of Schindleria, a character developing beyond the larval stages. The record of S. macrodentata is the first of the genus Schindleria for Indonesia and, at more than 100 km distant to the next shore, it is the first offshore record of a Schindler's fish. 


2020 ◽  
Vol 13 (1) ◽  

Spotted stinger individuals, Inimicus sinensis, collected from Carles, Iloilo, Philippines exhibited previously-unreported sexual dimorphism. Thirty-three morphological measurements, including standard length, and fourteen meristic counts from 99 specimens (47 males and 52 females) were analyzed for sexual dimorphism. Most morphometric characters differed significantly between the sexes, whereas no differences were found in meristic counts. Dorsal and anal-fin and free pectoral-fin ray lengths were greater in male specimens. On the other hand, the head and body region were relatively larger in female specimens. Principal Component Analysis (PCA) extracted two principal components from significantly different parameters, which explained 62.29 % of the cumulative variances. Variations in the two major components resulted from: head width, upper jaw, lower jaw, snout, pre-dorsal, pre-anal-fin, and anal-fin base lengths in PC1 (45.65 %); and orbit diameter and anal-fin base length in PC2 (16.64 %). Additionally, a single anterolateral pore on the body and pores above the lateral-line are described, although no evidence of association with other organs was found.


Zootaxa ◽  
2008 ◽  
Vol 1839 (1) ◽  
pp. 60 ◽  
Author(s):  
HEOK HEE NG ◽  
WALTER J. RAINBOTH

Glyptothorax coracinus sp. nov. is described from the western face of the Krâvanh (Cardamom) Mountains and Dâmrei (Elephant) Mountains in southwestern Cambodia. It can be distinguished from congeners by its color pattern consisting of blackish brown body with indistinct pale longitudinal stripes on the lateral line and mid-dorsal regions of the body, pale markings on the nuchal plate absent, length of adipose-fin base 12.3–14.5% SL, length of caudal peduncle 18.6– 21.0% SL, depth of caudal peduncle 7.9–9.4% SL, body depth at anus 11.0–14.6% SL, eye diameter 6.3–7.2% HL, 36– 37 vertebrae, tubercles on the dorsal surface of the head with a single, median ridge, and anastomosing striae absent on thoracic adhesive apparatus that does not reach the level of the base of the last pectoral-fin ray.


Zootaxa ◽  
2011 ◽  
Vol 2823 (1) ◽  
pp. 61 ◽  
Author(s):  
HEOK HEE NG ◽  
DANG KHANH HONG ◽  
NGUYEN VAN TU

Clarias gracilentus, a new Southeast Asian walking catfish species, is described from Phu Quoc Island (Vietnam) off the coast of southeastern Cambodia and from mainland southeastern Cambodia. The new species is a member of the C. nieuhofii species complex, and can be distinguished from congeners in the complex in having a combination of: head width 11.9–12.9% SL, distance between the occipital process and the base of the first dorsal-fin ray 5.3–8.4% SL, pectoral-fin length 8.5–10.1% SL, body depth at anus 8.2–11.7% SL, pelvic-fin length 4.3–5.5% SL, length of anal-fin base 60.0–63.9% SL, eye diameter 5.4–7.2% HL, interorbital distance 42.7–48.0% HL, occipital-process length 7.8–14.7% HL, 96–101 dorsal-fin rays, 84–89 anal-fin rays and 80–84 total vertebrae.


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