The lateral line system and its innervation in the Japanese eel Anguilla japonica (Teleostei: Elopomorpha: Anguillidae).

The lateral line system and its innervation were examined in the Japanese eel Anguilla japonica. Although the species has seven lateral line canals and 13 superficial neuromast groups, the components are generally similar to those in many other teleosts. The lateral line system of A. japonica is distinctive in having a rostral commissure connecting the left and right supraorbital canals, pouches in the cephalic lateral line canals and superficial neuromasts along the lower lip, and lacking a postotic canal. Four tube-like elements, two along the supratemporal canal and the other two along the temporal portion of the trunk canal, respectively, are also reported. The functional significance of cephalic lateral line pouches, homologies of the four tube-like elements, and other distinctive characters are discussed.

The paedomorphic lateral line system in Pseudamiops and Gymnapogon (Percomorpha, Apogonidae), with morphological and molecular-based phylogenetic considerations.

The lateral line system and its innervation were examined in two paedomorphic species of Apogonidae, Gymnapogon japonicus and Pseudamiops cf. springeri, both of which have been included in Gymnapogonini (Apogoninae) characterized by a small translucent body lacking canalized lateral line scales, but with many superficial neuromasts (total SNs: 2,691 and 2,197 in G. japonicus and Pseudamiops cf. springeri, respectively). Although scales are entirely absent in G. japonicus, the innervation pattern of the trunk lateral line system is basically similar to that in other apogonids having a single lateral line scale series. In comparison, Pseudamiops cf. springeri (and P. gracilicauda) have three series of inconspicuous lateral line scales with a distinct innervation pattern, implying a phylogenetic affinity with Pseudamia (Pseudamiinae). The monophyly of Pseudamiops and Pseudamia was also supported strongly by a molecular phylogenetic analysis, thus the paedomorphic nature is considered homoplasy between Pseudamiops and Gymnapogon. The innervation of head lateral line system in G. japonicus and Pseudamiops cf. springeri is basically the same with that of other apogonids, supporting homology of the presence of many head SNs among the species. The SN pattern and head canals of adult Pseudamiops cf. springeri are similar to those in juvenile Pseudamia gelatinosa, implying a paedomorphic truncation of lateral line system development in Pseudamiops cf. springeri.

Convergent evolution of the lateral line system in Apogonidae (Teleostei: Percomorpha) determined from innervation.

The lateral line system and its innervation were examined in two species of the family Apogonidae (Cercamia eremia [Apogoninae] and Pseudamia gelatinosa [Pseudamiinae]). Both species were characterized by numerous superficial neuromasts (SNs; total 2,717 in C. eremia; 9,650 in P. gelatinosa), including rows on the dorsal and ventral halves of the trunk, associated with one (in C. eremia) and three (in P. gelatinosa) reduced trunk canals. The pattern of SN innervation clearly demonstrated that the overall pattern of SN distribution had evolved convergently in the two species. In C. eremia, SN rows over the entire trunk were innervated by elongated branches of the dorsal longitudinal collector nerve (DLCN) anteriorly and lateral ramus posteriorly. In P. gelatinosa, the innervation pattern of the DLCN was mirrored on the ventral half of the trunk (ventral longitudinal collector nerve: VLCN). Elongated branches of the DLCN and VLCN innervated SN rows on the dorsal and ventral halves of the trunk, respectively. The reduced trunk canal(s) apparently had no direct relationship with the increase of SNs, because these branches originated deep to the lateral line scales, none innervating canal neuromast (CN) homologues on the surface of the scales. In P. gelatinosa, a CN (or an SN row: CN homologue) occurred on every other one of their small lateral line scales, while congeners (P. hayashii and P. zonata) had an SN row (CN homologue) on every one of their large lateral line scales.

Muscular system in the pacific bluefin tuna Thunnus orientalis (Teleostei: Scombridae).

The muscular system in the Pacific bluefin tuna Thunnus orientalis is studied in detail. For the first time, a complete description of the muscular anatomy of a thunnid is provided here. Eighty-two elements including subdivisions of components of the muscular system are identified. This is less than found in a basal perciform and two other investigated scombrid species, owing mainly to the absence or fusion of pectoral, pelvic and caudal fin muscles. The absence of elements of the basal perciform pattern was most prominent in the caudal fin, which includes only the flexor dorsalis, flexor ventralis, hypochordal longitudinalis, and interradialis. In the caudal fin, the medial fan-shaped ray was identified as the first dorsal ray, judging from myological and neuroanatomical characters. The highly developed gill filament muscles in Thunnus orientalis and sheet-like rectus communis control gill ventilation. Long body muscle tendons reduce the metabolic energy needed during rapid and continuous swimming. These characters are interpreted as adaptations in the context of the oceanic life style of the species.

Homologies of the branchial arch muscles in Zacco platypus (Teleostei: Cypriniformes: Cyprinidae): evidence from innervation pattern.

Homologies of the branchial arch muscles in the cyprinid Zacco platypus are assessed based on their innervation. Muscles serving the first gill arch are innervated by branches of the glossopharyngeal (IX) nerve and those serving other arches by the vagal (X) nerve. Absence of the levator posterior is confirmed. Five pairs of muscles originating from the cranium and inserted onto the specialized 5th ceratobranchial, all unique to cyprinids, are innervated by the 4th branchial trunks of X, indicating that all pairs are derivatives of the sphincter oesophagi, involving reorganization from intrinsic to extrinsic elements. Homologies of some ventral branchial muscles are also discussed and the criteria for homology improved by clarifying the innervation pattern.

Lateral line system and its innervation in Tetraodontiformes with outgroup comparisons: descriptions and phylogenetic implications.

The lateral line system and its innervation in ten tetraodontiform families and five outgroup taxa were examined. Although some homology issues remained unresolved, tetraodontiforms were characterized by having two types (at least) of superficial neuromasts (defined by the presence or absence of supporting structures) and accessory lateral lines and neuromasts (except Molidae in which "accessory" elements were absent). The preopercular line in Tetraodontiformes was not homologous with that of typical teleosts, because the line was innervated by the opercular ramule that was newly derived from the mandibular ramus, the condition being identical to that in Lophiidae. Within Tetraodontiformes, the number of neuromasts varied between 70 and 277 in the main lines and between 0 and 52 in accessory elements. Variations were also recognized in the presence or absence of the supraorbital commissure, mandibular line, otic line, postotic line, ventral trunk line, and some lateral line nerve rami, most notably the dorsal branch of the opercular ramule, being absent in Aracanidae, Ostraciidae, Tetraodontidae, Diodontidae, and Molidae. Morphological characteristics derived from the lateral line system and its innervation provided some support for a sister relationship of tetraodontiforms with lophiiforms.

Branchial arch muscle innervation by the glossopharyngeal (IX) and vagal (X) nerves in tetraodontiformes, with special reference to muscle homologies.

Branchial arch muscle innervation by the glossopharyngeal (IX) and vagal (X) nerves in 10 tetraodontiform families and five outgroup taxa was examined, with special reference to muscle homologies. Basic innervation patterns and their variations were described for all muscle elements (except gill filament muscles). In the tetraodontids Takifugu poecilonotus and Canthigaster rivulata, diodontid Diodon holocanthus, and molid Mola mola, levator externus 4 was innervated by the 3rd vagal branchial trunk (BX3) in addition to BX2, owing to strong posterior expansion of the muscle. Based on nerve innervation, migrations of the muscle attachment sites (i.e., origins and insertions) were recognized in levator internus 2 (in Mola mola), obliquus dorsalis 3 (in Ostracion immaculatus and Canthigaster rivulata), and obliquus ventralis 2 (in Stephanolepis cirrhifer), muscle topologies not necessarily being indicative of homologies. Embryonic origin of the retractor dorsalis and parallel attainment of the swimbladder muscle within the order were also discussed.