Gerres limbatus Cuvier and G. lucidus Cuvier from the Indo-Malay Archipelagos, the latter corresponding to young of the former (Perciformes: Gerreidae)

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.     

Redescriptions ofGerres baconensis (Evermann & Seale, 1907),G. equulus Temminck & Schlegel, 1844 andG. oyena (Forsskål, 1775), included in the “G. oyena complex”, with notes on other related species (Perciformes: Gerreidae)

The gerreid species,Gerres baconensis (Evermann &; Seale),G. equulus Temminck &; Schlegel andG. oyena (Forsskål), 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.     

Validity of the gerreid fish,Gerres macracanthus Bleeker, 1854, with designation of a lectotype,and designation of a neotype forG. filamentosus Cuvier, 1829

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.     

A new species,gerres infasciatus, from the gulf of thailand (perciformes: Gerreidae)

Gerres infasciatus sp. nov. is described from the holotype and two paratypes, 125–140 mm in standard length (SL), collected off Samut Prakan, northern Gulf of Thailand. The species is similar toG. filamentosus Cuvier andG. macracanthus Bleeker in general appearance, having an elongated second dorsal fin spine, but differs from them in having 39 or 40 pored lateral line scales, the first and second soft dorsal fin ray tips yellow in fresh specimens, a narrow, faint dusky-yellowish margin on the upper membrane of the spinous dorsal fin (between 4th–9th spines), the distal part of the pelvic fin (between 1st–5th soft rays) white for 1/3–1/2 of each ray length (lost after preservation), bands absent on the body in both fresh and preserved specimens, a smaller orbit diameter (11.4–12.4% of SL), a longer second dorsal fin spine (48.0–68.9% of SL), and shorter second and third anal fin spines (10.7–11.2% and 10.4–11.3% of SL), respectively.     

Larval, prejuvenile and juvenile development of Eucinostomus currani

Larval and juvenile Eucinostomus currani are described based on pigmentation, meristics and morphometric characteristics of 198 specimens collected in Bahía de La Paz and Ensenada de La Paz, B.C.S., Mexico. Diagnostic characteristics are the presence of head melanophores and several punctuate melanophores scattered over the lateral surface of the gut from early stages, a tricolour pigment pattern forming on the dorsal fin in postflexion stage and black stripes on the flanks of prejuveniles and juveniles.     

A review of the <Emphasis Type="Italic">Gerres subfasciatus</Emphasis> complex from the Indo-West Pacific,with three new species (Perciformes: Gerreidae)

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 Günther, 1859, and Gerres kapas Bleeker, 1854, are recognized as junior synonyms of G. subfasciatus and Gerres oyena (Forsskål, 1775), respectively. All species (except G. oyena) have a small (<170?mm in standard length: SL), moderately deep (depth 36–48% SL), body with dark vertical bars, dorsal fin rays X, 9 or IX, 10, and 31/2 or 41/2 scale rows between the 5th dorsal fin spine base and lateral line, defined as the G. subfasciatus complex. The five species can be variously differentiated from each other by dorsal head squamation, and differing meristic, morphometric, and color characters. They are generally distributed sympatrically in the Indo-West Pacific. Other nominal species of uncertain status or relationship are discussed.     

Description ofGerres chrysops sp. nov. From Thailand and redescription ofGerres setifer (Hamilton, 1822) andG. Decacanthus (Bleeker, 1865) (perciformes: Gerreidae)

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.     

Relationships among four genera of mojarras (Teleostei: Perciformes: Gerreidae) from the western Atlantic and their tentative placement among percomorph fishes

A phylogenetic study of the percoid family Gerreidae at both lower and higher taxonomic levels is presented based on DNA sequence data of four genes: mitochondrial 12S and 16S, and nuclear genes rhodopsin and recombination activating gene 1 (RAG1). The taxonomic sampling includes four genera of Gerreidae from the western Atlantic, 39 additional percomorph representatives and two outgroups. Phylogenetic results confirm the monophyly of the Gerreidae and suggest that the family is divided into two sub-groups ( Diapterus auratus plus Eugerres plumieri and Eucinostomus gula plus Gerres cinereus ), which correspond to two previously defined taxonomic assemblages characterized by the shape of the preoperculum. Gerreids are placed at an intermediate position in the percomorph tree between two basal clades (L and Q) and a terminal clade N (grouping tetraodontiforms, acanthuroids, lophiiforms, caproids and several percoids). In addition, topology tests indicate that two traditional assemblages, Labroidei (seven representatives sampled) and Percoidei (22 representatives sampled) are not natural groups. Labrids and scarids appear to be more closely related to gerreids and to the members of clade N than to any other basal percomorphs, including their labroid 'allies' sampled in this study, Embiotocidae, Pomacentridae and Cichlidae, which are all nested within clade Q that also includes atherinomorphs, mugiliforms and Chandidae. The percoid taxa included in this study are widely distributed among various percomorph lineages. The percomorph phylogeny obtained is highly congruent with results from recent molecular studies.     

A new species: Gerres microphthalmus (Perciformes: Gerreidae) from Japan with notes on limited distribution, included in the “G. filamentosus complex”

 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. Received: June 28, 2001 / Revised: November 13, 2001 / Accepted: December 10, 2001     

Saline acclimation of striped mojarra <Emphasis Type="Italic">Eugerres plumieri</Emphasis> (Cuvier 1830) and optimal dosage of carp pituitary extract (CPE) to induce spawning

The main objective of the current study was to determine an optimal dosage of commercial carp pituitary extract (CPE) of the conventional heteroplastic hypophysation technique to induce spawning in the wild caught striped mojarra broodstock Eugerres plumieri under laboratory conditions. We also describe trials testing saline acclimation regimes (changes from 10‰ to 30‰) prior to hormonal induction. For saline acclimation, three treatments were performed: first and second treatments began 1-day after conditioning of broodstock fish with a total duration of the saline changes lasting 1-day and 2-days, respectively. The third treatment began 30-days after conditioning with a 7-day saline regime. After reaching 30‰, all fish from the first and second treatments died after the fourth and ninth days, respectively; while the fishes in the third treatment survived more than two years. These fish remain on public exhibit in the “Mundo Marino” Aquarium, Santa Marta, Colombia. Four treatments of hormonal induction were tested on females using a total concentration of 5-mg of CPE per kg of body weight: first, second and third treatments were applied in two hormonal doses that corresponded to 10%–90%, 30%–70% and 40%–60%, respectively, with time intervals between doses of 14-h for the first and second treatment and of 12-h for the third treatment. The fourth treatment was applied in four hormonal doses that it corresponded to 20%–20%–30%–30% with 12-h time intervals between doses. Only the fishes of the fourth treatment resisted the induction, continued to live and reached spawning artificially. Water temperature remained at 28 ± 1°C and at 30‰ salinity during the study. The “dry” method of fertilization was used. The fertilized eggs were incubated at 30‰ and 35‰ salinities. These eggs reached the Morula early stage, but were later attacked by protozoan. These results suggest that fast changes of saline and limited hormonal dosages do not offer effective results in Eugerres plumieri. This work provided fundamental procedures for the culture and maintenance of live broodstock for striped mojarra in saltwater and/or coastal lagoon habitats and provides an effective and viable dosage of CPE for artificial spawning and commercial production in this species.