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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.

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.

Vertebral bodies of teleost fish are formed by the sclerotomal bone covering the chordacentrum. The internal part of the sclerotomal bone is composed of an amphicoelous hourglass shaped autocentrum, which is common in most fish species. In contrast, the external shape of the sclerotomal bone varies extensively among species. There are multiple hypotheses regarding the composition and formation of the external structure. However, as they are based on studies of few extant or extinct species, their applicability to other species remains to be clarified. To understand the morphology, formation, and composition of vertebral bodies in teleosts, we performed a comparative analysis using micro‐CT scans of 32 species from 10 orders of Teleostei and investigated the detailed morphology of the sclerotomal bone, especially its plate‐like ridge and trabeculae. We discovered two structural characteristics that are shared among most of the examined species. One was the sheet‐like trabeculae that extend radially from the center of the vertebral body with a constant thickness. The other was the presence of hollow spaces on the internal parts of the lateral ridge and trabeculae. The combination of different arrangements of sheet‐like trabeculae and internal hollow spaces formed different shapes of the lateral structure of the vertebral body. The properties of these two characteristics suggest that the external part of the sclerotomal bone grows outward by deposition at the bone tip, and that, concurrently, bone absorption occurs in the internal part of the sclerotomal bone. The vertebral arches were also formed by the sheet‐like trabeculae, indicating that both, the vertebral body and the arches, are formed by the same component. The micro‐CT scanning data were uploaded to a public database so they can be used for future studies on fish vertebrae.

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 cephalic lateral line system and its innervation were examined and compared between the ocular and blind sides in Pardachirus pavoninus (Soleidae). On the ocular side, the otic and preopercular canals were partly (posteriorly and dorsally, respectively) formed by canalized scales (one and five, respectively), each containing a canal neuromast (i.e., “lateral line scales”) and innervated by the anterior lateral line nerve (otic and mandibular rami, respectively). The canal neuromasts of the five scales were recognized as homologous with superficial neuromasts in other taxa based on innervation. The scales, each with a canal perpendicular to the long axis of the scale, bridged the wide gap between the otic region of the cranium and preopercle. The superficial ophthalmic ramus was bifurcated on both sides, the dorsal ramule emerging from the cranium via a frontal foramen. The buccal ramus on the blind side was intensively ramified in the area made available by migration of the eye to the ocular side. The numbers of canal and superficial neuromasts differed greatly between the sides, being 19 and 173 on the ocular side, and 1 and 465 on the blind side, respectively. Sensory strips of superficial neuromasts on the blind side had clear long and short axes. Numerous dermal papillae occurred on the blind side, forming complex channels, according to directions of the long axes.