The mitochondrial genome of the spinyhead croaker Collichthys lucida: genome organization and phylogenetic consideration

The complete mitochondrial genome of the spiny head croaker Collichthys lucida was determined in the present study. The mitochondrial DNA was 16,442 base pairs in length, and contained 13 protein coding genes, 22 transfer RNAs, 2 ribosomal RNAs, and one major non-coding control region, with the content and order of genes being similar to those in typical teleosts. Most of the genes of C. lucida were encoded on the H-strand, while the ND6 and eight tRNA (Gln, Ala, Asn, Cys, Tyr, Ser (UCN), Glu and Pro) genes were encoded on the L-strand. The reading frames of two pairs of genes overlapped: ATPase 8 and 6 and ND4L and ND4 by ten and seven nucleotides, respectively. The control region was unusually short at only 768bp, and absence of typical conserved blocks (CSB-D, CSB-E, and CSB-F). Phylogenetic analyses indicated that C. lucida was located in the cluster of fish species from the family Sciaenidae, supporting the traditional taxonomic classification of fish, and in the cluster of Serranidae, the divergence time in Plectropomus leopardus is longer than that among its coordinal species. On the other hand, phylogenetic analyses do not support the monophyletic of family Centracanthidae and genera Larimichthys and Collichthys, which is against the morphological results.     

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.     

Early ontogeny of coal grunter from hormone-induced spawnings and laboratory-reared embryos and larvae

Spawning of coal grunter Hephaestus carbo was successfully induced using doses of human chorionic gonadotrophin (hCG) between 500 and 3000 IU kg (body weight)⁻¹. Water hardened eggs are telolecithal, amber in colour, spherical, transparent, demersal and slightly adhesive with a single large oil droplet and perivitelline space 47% of total egg volume. Cleavage begins 10–15 min after fertilization. Epiboly begins 6h after fertilization and continues for 4 h. Invagination of the neural tube is apparent 11·5 h after fertilization, followed by progressive organogenesis up to hatching 60–80 h after fertilization. An invagination in the yolk, consistent in shape, position and time of appearance among embryos spawned from numerous brood stock pairs, was visible in all fertilized eggs between neurulation (11-5 h) and early organogenesis (20 h). The functional significance of this yolk invagination is unknown. Newly-hatched larvae (4·2 mm L _T) are elongate and possess well developed eyes, a functional mouth, and a large yolk sac. Yolk is fully resorbed and first feeding occurs at 6 days posthatching. The sequence of fin formation is caudal, second dorsal and anal, first dorsal, pectoral and pelvic. The prefiexion larval stage lasts for c. 8 days and flexion of the notochord is complete within a further 8–9 days. Squamation commences at 30 days posthatching and transition to the juvenile life stage is complete by 35–40 days posthatching.