Morphology and development of the multiple lateral line canals on the trunk in two species of Hexagrammos (Scorpaeniformes,Hexagrammidae)

The morphology and development of the multiple lateral line canals (canals 1–5 in dorsal to ventral sequence) on the trunk of two representative hexagrammids, Hexagrammos decagrammus and H. stelleri, were studied using histological and cleared and stained material. The morphology of the lateral line scales of which the lateral line canals are composed and the distribution of canal neuromasts within them were described quantitatively. We hypothesized that 1) one neuromast is contained in each lateral line scale and all five canals contain neuromasts, 2) all five canals develop similarly, and 3) the multiple trunk canals are an adaptation for the alteration of lateral line function. Lateral line scale morphology was found to be similar among the five canals in Hexagrammos decagrammus and H. stelleri. However, canal 3 is significantly wider than the other four canals. It is the only one of the five canals connected to the canals on the head, and more significantly, it is the only one of the five canals that contains neuromasts. The lateral line scales that comprise all five lateral line canals show the same pattern of development whether or not they contain neuromasts. The five canals develop asynchronously, and each of the canals develops either rostro-caudally or caudo-rostrally. Canal 3 is the homologue of a single trunk canal in other teleosts; canals 1, 2, 4, and 5 are apomorphic features of the two species of Hexagrammos. Canals 1, 2, 4, and 5 cannot be functional components of the lateral line system because they do not contain neuromasts and thus cannot be adaptations for the alteration of lateral line function. The occurrence of lateral line canals lacking neuromasts demands a direct assessment of neuromast distributions in the lateral line canals among fishes. Finally, our data suggest that the putative role of neuromasts in the morphogenesis of lateral line canals and the nature of neuromast-bone relationships need to be critically reevaluated. J. Morphol. 233:195–214, 1997. © 1997 Wiley-Liss, Inc.     

Post‐embryonic development of canal and superficial neuromasts and the generation of two cranial lateral line phenotypes

The relatively simple structural organization of the cranial lateral line system of bony fishes provides a valuable context in which to explore the ways in which variation in post‐embryonic development results in functionally distinct phenotypes, thus providing a link between development, evolution, and behavior. Vital fluorescent staining, histology, and scanning electron microscopy were used to describe the distribution, morphology, and ontogeny of the canal and superficial neuromasts on the head of two Lake Malawi cichlids with contrasting lateral line canal phenotypes (Tramitichromis sp. [narrow‐simple, well‐ossified canals with small pores] and Aulonocara stuartgranti [widened, more weakly ossified canals with large pores]). This work showed that: 1) the patterning (number, distribution) of canal neuromasts, and the process of canal morphogenesis typical of bony fishes was the same in the two species, 2) two sub‐populations of neuromasts (presumptive canal neuromasts and superficial neuromasts) are already distinguishable in small larvae and demonstrate distinctive ontogenetic trajectories in both species, 3) canal neuromasts differ with respect to ontogenetic trends in size and proportions between canals and between species, 4) the size, shape, configuration, physiological orientation, and overall rate of proliferation varies among the nine series of superficial neuromasts, which are found in both species, and 5) in Aulonocara, in particular, a consistent number of canal neuromasts accompanied by variability in the formation of canal pores during canal morphogenesis demonstrates independence of early and late phases of lateral line development. This work provides a new perspective on the contributions of post‐embryonic phases of lateral line development and to the generation of distinct phenotypes in the lateral line system of bony fishes. J. Morphol. 277:1273–1291, 2016. © 2016 Wiley Periodicals, Inc.     

Development of the lateral line canal system through a bone remodeling process in zebrafish

The lateral line system of teleost fish is composed of mechanosensory receptors (neuromasts), comprising superficial receptors and others embedded in canals running under the skin. Canal diameter and size of the canal neuromasts are correlated with increasing body size, thus providing a very simple system to investigate mechanisms underlying the coordination between organ growth and body size. Here, we examine the development of the trunk lateral line canal system in zebrafish. We demonstrated that trunk canals originate from scales through a bone remodeling process, which we suggest is essential for the normal growth of canals and canal neuromasts. Moreover, we found that lateral line cells are required for the formation of canals, suggesting the existence of mutual interactions between the sensory system and surrounding connective tissues.     

Mechanosensory system of the lateral line in the subantarctic Patagonian blenny Eleginops maclovinus

This study describes the cephalic and trunk lateral line systems in Patagonian blenny Eleginops maclovinus juveniles, providing morphological details for pores, canals and neuromasts. Eleginops maclovinus juveniles possess a complete laterodorsal lateral line that extends from the upper apex of the gill opening along the trunk as far as the caudal fin. The lateral line was ramified through pores and canals. The following pores were recorded: four supraorbital pores, with two along the eye border and two on the snout; seven infraorbital pores, with three on the lacrimal bone and four being infraorbital; five postorbital pores, with three along the preopercular border (upper preoperculum branch) and two on the bone curvature (inferior preoperculum branch); and four mandibular pores aligned along the jaw. Furthermore, five narrow-simple and interconnected canals were found (i.e. preopercular, mandibular, supraorbital and infraorbital canals). Histologically, the dorsal lateral line presented thin neuromasts (350 μm) with short hair cells. By contrast, the cranial region presented long, thick neuromasts. Infraorbital and mandibular neuromasts had a major axis length of 260 μm and respective average diameters of 200 and 185 μm. Sensory system variations would be due to a greater concentration of neuromasts in the cranial region, allowing for a greater perception of changes in water pressure. Scarce morphological information is available for the lateral sensory system in Eleginopsidae, particularly compared to Channichthyidae, Bovichthydae, Artedidraconidae and Bathydraconidae. Therefore, the presented results form a fundamental foundation of knowledge for the lateral-line system in juvenile E. maclovinus and provide a basis for future related research in this taxon as well as within the Notothenioidei suborder.     

Morphology and ontogeny of multiple lateral‐line canals in the rock prickleback,Xiphister mucosus (Cottiformes: Zoarcoidei: Stichaeidae)

The structure and ontogeny of lateral‐line canals in the Rock Prickleback, Xiphister mucosus, were studied using cleared‐and‐stained specimens, and the distribution and morphology of neuromasts within lateral‐line canals were examined using histology. X. mucosus has seven cephalic canals in a pattern that, aside from four branches of the infraorbital canals, is similar to that of most teleostean fishes. Unlike most other teleosts, however, X. mucosus features multiple trunk lateral‐line canals. These include a short median posterior extension of the supratemporal canal and three paired, branching canals located on the dorsolateral, mediolateral, and ventrolateral surfaces. The ventrolateral canal (VLC) includes a loop across the ventral surface of the abdomen. All trunk canals, as well as the branches of the infraorbitals, are supported by small, dermal, ring‐like ossifications that develop independently from scales. Trunk canals develop asynchronously with the mediodorsal and dorsolateral canals (DLC) developing earliest, followed by the VLC, and, finally, by the mediolateral canal (MLC). Only the mediodorsal and DLC connect to the cephalic sensory canals. Fractal analysis shows that the complexity of the trunk lateral‐line canals stabilizes when all trunk canals develop and begin to branch. Histological sections show that neuromasts are present in all cephalic canals and in the DLC and MLC of the trunk. However, no neuromasts were identified in the VLC or its abdominal loop. The VLC cannot, therefore, directly function as a part of the mechanosensory system in X. mucosus. The evolution and functional role of multiple lateral‐line canals are discussed. J. Morphol. 276:1218–1229, 2015. © 2015 Wiley Periodicals, Inc.     

Innervation of the lateral line system in Rhyacichthys aspro: the origin of superficial neuromast rows in gobioids (Perciformes: Rhyacichthyidae)

The lateral line system and its innervation were examined in the most primitive gobioid taxon, Rhyacichthys aspro (Rhyacichthyidae). The infraorbital canal was present, whereas superficial neuromast rows a and c, typically present on the cheek of gobioids, were absent. Because the infraorbital canal (absent in other gobioids) and the two rows were commonly innervated by the buccal ramus, the latter were categorized as replaced rows from canal neuromasts. On an innervation basis, rows b and d on the cheek were considered to comprise superficial neuromasts only in all gobioids. The trunk lateral line system comprised canal and superficial neuromasts, the former being included in the lateral line scales (each bearing 1–7 neuromasts arranged longitudinally along the direction of a groove). Absence of bony roofs in the lateral line system was proposed as a synapomorphy of Gobioidei, and a progressive neotenic shift in the lateral line system of the suborder discussed.     

The lateral line receptor array of cyprinids from different habitats

The lateral line system of teleost fishes consists of an array of superficial and canal neuromasts (CN). Number and distribution of neuromasts and the morphology of the lateral line canals vary across species. We investigated the morphology of the lateral line system in four diurnal European cyprinids, the limnophilic bitterling (Rhodeus sericeus), the indifferent gudgeon (Gobio gobio), and ide (Leuciscus idus), and the rheophilic minnow (Phoxinus phoxinus). All fish had lateral line canals on head and trunk. The total number of both, CN and superficial neuromasts (SN), was comparable in minnow and ide but was greater than in gudgeon and bitterling. The ratio of SNs to CNs for the head was comparable in minnow and bitterling but was greater in gudgeon and ide. The SN‐to‐CN ratio for the trunk was greatest in bitterling. Polarization of hair cells in CNs was in the direction of the canal. Polarization of hair cells in SNs depended on body area. In cephalic SNs, hair cell polarization was dorso‐ventral or rostro‐caudal. In trunk SNs, it was rostro‐caudal on lateral line scales and dorso‐ventral on other trunk scales. On the caudal fin, hair cell polarization was rostro‐caudal. The data show that, in the four species studied here, number, distribution, and orientation of CNs and SNs cannot be unequivocally related to habitat. J. Morphol. 275:357–370, 2014. © 2013 Wiley Periodicals, Inc.     

Morphology of the Mechanosensory Lateral Line System in Elasmobranch Fishes: Ecological and Behavioral Considerations

The relationship between morphology of the mechanosensory lateral line system and behavior is essentially unknown in elasmobranch fishes. Gross anatomy and spatial distribution of different peripheral lateral line components were examined in several batoids (Raja eglanteria, Narcine brasiliensis, Gymnura micrura, and Dasyatis sabina) and a bonnethead shark, Sphyrna tiburo, and are interpreted to infer possible behavioral functions for superficial neuromasts, canals, and vesicles of Savi in these species. Narcine brasiliensis has canals on the dorsal surface with 1 pore per tubule branch, lacks a ventral canal system, and has 8–10 vesicles of Savi in bilateral rows on the dorsal rostrum and numerous vesicles ( = 65 ± 6 SD per side) on the ventral rostrum. Raja eglanteria has superficial neuromasts in bilateral rows along the dorsal body midline and tail, a pair anterior to each endolymphatic pore, and a row of 5–6 between the infraorbital canal and eye. Raja eglanteria also has dorsal canals with 1 pore per tubule branch, pored and non-pored canals on the ventral surface, and lacks a ventral subpleural loop. Gymnura micrura has a pored dorsal canal system with extensive branch patterns, a pored ventral hyomandibular canal, and non-pored canal sections around the mouth. Dasyatis sabina has more canal pores on the dorsal body surface, but more canal neuromasts and greater diameter canals on the ventral surface. Sphyrna tiburo has primarily pored canals on both the dorsal and ventral surfaces of the head, as well as the posterior lateral line canal along the lateral body surface. Based upon these morphological data, pored canals on the dorsal body and tail of elasmobranchs are best positioned to detect water movements across the body surface generated by currents, predators, conspecifics, or distortions in the animal's flow field while swimming. In addition, pored canals on the ventral surface likely also detect water movements generated by prey. Superficial neuromasts are protected from stimulation caused by forward swimming motion by their position at the base of papillar grooves, and may detect water flow produced by currents, prey, predators, or conspecifics. Ventral non-pored canals and vesicles of Savi, which are found in benthic batoids, likely function as tactile or vibration receptors that encode displacements of the skin surface caused by prey, the substrate, or conspecifics. This mechanotactile mechanism is supported by the presence of compliant canal walls, neuromasts that are enclosed in wide diameter canals, and the presence of hair cells in neuromasts that are polarized both parallel to and nearly perpendicular to the canal axis in D. sabina. The mechanotactile, schooling, and mechanosensory parallel processing hypotheses are proposed as future directions to address the relationships between morphology and physiology of the mechanosensory lateral line system and behavior in elasmobranch fishes.     

Functional morphology of the piper Hyporhamphus ihi with reference to the role of the lateral line in feeding

As a basis for understanding the function of the halfbeak of the piper Hyporhamphus ihi (Phillips), details of the structure and dimensions of the anterior lateral line on the head and lower jaw of the piper are described. The anterior lateral line is composed of a series of cranial canals; the supraorbital-postorbital canal; the suborbital canal; and the preopercular-mandibular canal which extends along the lower jaw. Each canal opens to the surface by a series of pores, and individual neuromasts exist in specialized regions of the canals between each of the pores. Piper are nocturnal plankivores and they possess the feeding structures and digestive tract suited to this diet. The hypothesis is proposed that they use the anterior lateral line system in prey detection, and this paper shows that the piper's elongate body form, swimming behaviour, and lack of a specialized visual system are all consistent with this hypothesis.     

Lateral line system in the triplefin Enneapterygius etheostomus (Perciformes: Tripterygiidae): new implications for taxonomic studies

The lateral line system, including the distribution and counts of canal and superficial neuromasts, in a Japanese tripterygiid Enneapterygius etheostomus was studied. Although the basic topography of the lateral line canals was typical of teleosts, preopercular, mandibular, parietal, predorsal and caudal fin groupings of superficial neuromasts were recognized for the first time in addition to the previously reported groupings in Tripterygiidae. Comparisons of neuroanatomical characteristics with those of New Zealand tripterygiids previously reported revealed significant differences, thereby indicating that detailed examination of the lateral line system could provide new information useful for taxonomic studies.     

Morphology of the mechanosensory lateral line system in the Atlantic Stingray,Dasyatissabina: The mechanotactile hypothesis

The biological function of anatomical specializations in the mechanosensory lateral line of elasmobranch fishes is essentially unknown. The gross and histological features of the lateral line in the Atlantic stingray, Dasyatis sabina, were examined with special reference to its role in the localization and capture of natural invertebrate prey. Superficial neuromasts are arranged in bilateral rows near the dorsal midline from the spiracle to the posterior body disk and in a lateral position along the entire length of the tail. All dorsal lateral line canals are pored, contain sensory neuromasts, and have accessory lateral tubules that most likely function to increase their receptive field. The pored ventral canal system consists of the lateral hyomandibular canal along the disk margin and the short, separate mandibular canal on the lower jaw. The extensive nonpored and relatively compliant ventral infraorbital, supraorbital, and medial hyomandibular canals form a continuous complex on the snout, around the mouth, and along the abdomen. Vesicles of Savi are small mechanosensory subdermal pouches that occur in bilateral rows only along the ventral midline of the rostrum. Superficial neuromasts are best positioned to detect water movements along the transverse body axis such as those produced by tidal currents, conspecifics, or predators. The pored dorsal canal system is positioned to detect water movements created by conspecifics, predators, or possibly distortions in the flow field during swimming. Based upon the stingray lateral line morphology and feeding behavior, we propose the Mechanotactile Hypothesis, which states that the ventral nonpored canals and vesicles of Savi function as specialized tactile mechanoreceptors that facilitate the detection and capture of small benthic invertebrate prey. J. Morphol. 238:1–22, 1998. © 1998 Wiley-Liss, Inc.     

Lateral line reception in still- and running water

The lateral line of fish is composed of neuromasts used to detect water motions. Neuromasts occur as superficial neuromasts on the skin and as canal neuromasts in subepidermal canals. Fibres of the lateral line nerves innervate both. There have been extensive studies on the responses of lateral line nerve fibres to dipole stimuli applied in still water. However, despite the fact that many fish live in rivers and/or swim constantly, responses of lateral line nerve fibres to dipole stimuli presented in running water have never been recorded. We investigated how the peripheral lateral line of still water fish ( Carassius auratus) and riverine fish ( Oncorhynchus mykiss) responds to minute sinusoidal water motions while exposed to unidirectional water flow. Both goldfish and trout have two types of posterior lateral line nerve fibres: Type I fibres, which most likely innervate superficial neuromasts, were stimulated by running water (10 cm s(-1)). The responses of type I fibres to water motions generated by a vibrating sphere were masked if the fish was exposed to running water. Type II fibres, which most likely innervate canal neuromasts, were not stimulated by running water. Consequently, responses of type II fibres to a vibrating sphere were not masked under flow conditions.     

Ontogeny and phylogeny of the trunk lateral line system in cichlid fishes

An examination of the ontogeny of the lateral line trunk canal and the diversity of adult trunk canal patterns among cichlids indicates that bidirectional canal formation is a general ontogenetic pattern in the Cichlidae with the exception of Cichla and those few species with a complete trunk canal pattern. In addition to the tubed scales which make up the trunk canal, some lateral line scales have pits containing superficial neuromasts. These are recognized as components of the lateral line system of the trunk in adult cichlids for the first time. Eight trunk canal patterns that are variations on a simple disjunct pattern are defined among the 17 cichlid genera examined. Using bidirectional canal formation as a developmental model, these patterns can be placed along an ontogenetic spectrum. This suggests that heterochrony (alterations in the timing of development) is an important mechanism of evolutionary change in the lateral line system of the trunk in cichlid fishes.     

西伯利亚鲟仔鱼侧线系统的发育

鲟鱼属软骨硬鳞鱼,在电感受器的进化中占据着极为重要的地位。该文以光镜和扫描电镜手段研究了西伯利亚鲟侧线系统早期发育,包括侧线基板发育及感觉嵴的形成、侧线感受器的发育和侧线管道的形成。1日龄,听囊前后外胚层增厚区域出现6对侧线基板;除后侧线基板细胞向躯干侧面迁移外,其他侧线基板均形成感觉嵴结构;每一侧线基板中均有神经丘原基形成。7日龄,壶腹器官在吻部腹面两侧出现,壶腹器官的发育比神经丘晚一周左右。9日龄,神经丘下的表皮略有凹陷,侧线管道开始形成。29日龄,在吻部腹面两侧可见少数个别的壶腹器官表皮细胞覆盖壶腹器官中央区域留下3～4个小的开口;壶腹管内可见大量的微绒毛存在,在其他鲟形目鱼类、软骨鱼类中也存在类似的结构。57日龄,躯干侧线管道已完全埋于侧骨板中;壶腹器官主要分布在吻部腹面,3～4个聚集在一起,呈"梅花状",分布紧密,并且该部分皮肤表面凹陷,形成花朵状凹穴;侧线系统发育完善。     

A comparison of Lateral Line Morphology of Blue Cod and Torrentfish: Two Sandperches of the Family Pinguipedidae

Parapercis colias (blue cod) and Cheimarrichthys fosteri (torrentfish) are two members of the family Pinguipedidae. They reside in habitats with different background levels of hydrodynamic activity and differ in their feeding ecology. The peripheral morphology of the mechanosensory lateral line system was investigated in each species. The torrentfish is the only freshwater member of this otherwise exclusively marine family. It resides in turbulent fast flowing habitats and feeds nocturnally on stream drift. Torrentfish have many superficial neuromasts and a simple unbranched canal system. In comparison the blue cod resides in sub-tidal slow flowing habitats, is a diurnal predator and has relatively few superficial neuromasts and a well-developed branching canal system. For these two species the background level of hydrodynamic activity does not appear to be the dominant selection pressure on lateral line morphology, in the case of the torrentfish in particular it is more compelling to view lateral line morphology in the light of environmental pressures that have favoured the evolution of nocturnal feeding.     

Sensory integration in the hydrodynamic world of rainbow trout

Water movements, of both abiotic and biotic origin, provide a wealth of information for fishes. They detect these water movements by arrays of hydrodynamic sensors located on the surface of the body as superficial neuromasts and embedded in subdermal lateral line canals. Recently, the anatomical dichotomy between superficial and canal neuromasts has been matched by demonstrations of a corresponding functional dichotomy. Superficial neuromasts are sensitive to water flows over the surface of the fish and are the sub-modality that participates in orientation to water currents, a behaviour known as rheotaxis. The canal neuromasts are sensitive to water vibration and it is this sub-modality that determines the localization of artificial prey. Recently, however, it has been shown that the complex behaviour of natural prey capture in the dark requires input from both lateral line sensory submodalities and here we show that the ability of trout to hold station behind a stationary object in fast flowing water also requires integration of information from both sub-modalities.     

The Sensory Canal Systems of the Living Coelacanth, Latimeria Chalumnae: A New Instalment

Entire sensory canal systems of the coelacanth, Latimeria chalumnae, are described: not only the course of principal canals with their primary and secondary collaterals, but also the course and branches of the pit-line and reticular canals. The number of pores on the left side of the head were found to be 296 in an early (yolksac) embryo, 321 in a late term fetus, 485 in a juvenile, and 2974 in adults. This means that in latimeria most of the lateral-line canal system develop after parturition. Pit lines of the living coelacanth are not rows of superficial neuromasts but canals covered by a thin epidermis like in other sensory canals of the lateral line. These pit-line canals, however, have a very specific structure and branching pattern: the medial dorsal pit-line canal is connected by fine branches on top of the head. The infra-dentary pit-line canal connects via these branches with canals deep inside the bones. Several fine and richly branched canaliculi of unknown function radiate from each quadratojugal pit-line canal. The gular plate pit-line canal has superficially branching arms as well as connections to numerous deeper canals inside the bone. These canals consist of fine branches that in turn lead to and open on the ventral surface of the gular plates as small pores. The system is reminiscent of the reticular (pore) canal system known only from some fossil agnathans and fishes. Thus latimeria combines the reticular system of ancient vertebrates with the lateral-line system of modern fishes. The significance of this gular (possibly electro-sensory) system for feeding by the coelacanth will be discussed.     

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.