Development of bony skeleton in the ontogeny of lumpfish Cyclopterus lumpus (Cyclopteridae,Scorpaeniformes)

The development of bony skeleton is studied in the ontogeny of lumpfish Cyclopterus lumpus. In general, the sequence of appearance of the bony elements is similar to that in other teleost fishes with the exclusion of the absence of the basihyal anlage and the presence of only cartilaginous basibranchials in all examined larvae and juveniles. Bony elements of the ventral sucking disc appear very early (together with the parasphenoid, maxilla, opercle, and cleithrum), and they are characterized by rapid development. The intercalar is observed in the neurocranium of the larvae. In late larvae and in juveniles, the anlage of the medial extrascapular fused with the parietal and the lateral extrascapular attached to the pterotic are registered. C. lumpus differs from Cyclopsis tentacularis and the species of the genus Eumicrotremus in the presence of the cutting in the upper margin of the ceratohyal instead of the berycoid opening. The larvae and juveniles of C. lumpus and C. tentacularis are characterized by the presence of a reduced spiny ray at the origin of the second dorsal fin, most likely, representing a plesiomorphy of the Cyclopteridae. In the larvae of C. lumpus and C. tentacularis of a similar size, the degree of development of skeletal elements is the same, which suggests a similar developmental rate of their skeletal elements.     

Relationships of eelpouts of the genus <Emphasis Type="Italic">Zoarces</Emphasis> (Zoarcidae,Pisces) inferred from molecular genetic and morphological data

Abstract-Molecular genetic and morphological analysis of eelpouts of the genus Zoarces was carried out. Based on the mitochondrial DNA sequence variation, haplotypes of notched-fin eelpout, Z. elogatus, more closely related Fedorov eelpout, Z. fedorovi, and common eelpout, Z. viviparus, as well as of Andriyashev eelpout, Z. andriashevi, were grouped in one macrocluster. Haplotypes of American eelpout, Z. americanus, and blotched eelpout, Z. gillii, clustered separately from other species. The genetic differences between Z. gillii and the other eelpout species were very high for within-genus comparisons, constituting 7.62%. Species divergence in terms of morphological characters was generally consistent with molecular genetic data and confirmed distinct isolation of American eelpout, and especially of blotched eelpout.     

Comparative osteology,relationships, and systematics of fish of the genus <Emphasis Type="Italic">Zoarces</Emphasis> (Zoarcidae,Perciformes)

Comparative-osteological investigation of all species of the genus Zoarces is made: Z. fedorovi, Z. andriashevi, Z. elongatus, Z. viviparus, Z. americanus, and Z. gillii. In the skeleton of hyoid arch in species of Zoarces, Lycozoarces, and Lycodes, paired bony elements are found, not described previously, identified as parurohyalia which may be synapomorphy of Zoarcidae. Differences between the Zoarces species are revealed by 56 external morphological and osteological characters. Cladistic analysis yielded one tree 135, Ci 0.57, Ri 0.54 long. Cladistic analysis confirms validity of a recently described species Z. fedorovi, which turned out to be the most generalized in the genus Zoarces, as well as the validity of Z. elongatus. The species Z. americanus and Z. gillii occupy a terminal position preventing their isolation to independent genera as was previously supposed, as this would lead to paraphyly of the genus Zoarces.     

Features of the biology of the eelpout <Emphasis Type="Italic">Zoarces fedorovi</Emphasis> (Perciformes: Zoarcidae) from Tauisk bay,Sea of Okhotsk

The results of long-term research on the biology of the viviparous Fedorov eelpout Zoarces fedorovi from the Tauiskaya Guba in the Sea of Okhotsk are generalized. It was determined that in winter and spring this species inhabits strongly freshened sea areas and in summer and fall it inhabits, as a rule, estuarine areas in the tide effect zone. Z. fedorovi did not leave the coastal zone, even during the ebb, and could remain in colder fresh water up to 12 h a day. Data on the age, sexual and size structure of the catches, character of linear growth, increase in body mass and fecundity, size, as well as the growth rates of the larvae and fry during prenatal development of Z. fedorovi are cited.     

Scaling of skeletal mass to body mass in fishes

The few available observations are consistent with the supposition that the relative weightlessness of fishes leads to isometric scaling of skeletal mass to body mass. To explore further this pattern we studied scaling in ontogeny with freshwater tilapia, Oreochromis nilotica, and in phylogeny with adult coral reef fishes. Body mass and skeletal mass were measured for freshly caught fishes. Data were transformed to logarithms and fitted to a power function with least-square linear regression. Whereas slope for all O. nilotica combined was consistent with isometry (b = 1.00; 95% CI = 0.02), slopes calculated separately for juveniles (b = 1.16; CI = 0.07) and adults (b = 1.10; CI = 0.07) indicated positive allometric scaling of the skeleton during ontogeny. The scaling pattern was isometric for a multispecies sample of perciform fishes from coral reefs (b = 0.82; CI = 0.21). However, the single perciform species with the largest number of individuals in the sample, Epinephelus guttatus, was positively allometric (b = 1.13; CI = 0.12), whereas the tetraodontiform, Balistes vetula, was isometric (b = 1.05; CI = 0.12). Instead of leading to isometry, weightlessness may increase the range of possibilities for the scaling of skeleton mass to body mass in fishes compared to terrestrial vertebrates. The scaling of the skeleton in fishes may be related to foraging style and manner of locomotion in water rather than be driven by the need to resist gravity. © 1996 Wiley-Liss, Inc.     

Nomenclature of cartilaginous elements in the caudal skeleton of teleostean fishes

Nomenclature and abbreviations are proposed for the cartilaginous elements of the caudal skeleton of teleostean fishes. These were developed on the basis of examination of 510 species within 198 families of 31 orders and the determination of the positional relationship between these structures and the bony elements. A review of the most important relative literature is also provided.     

Immunoglobulin light chain class multiplicity and alternative organizational forms in early vertebrate phylogeny

The prototypic chondrichthyan immunoglobulin (Ig) light chain type (type I) isolated from Heterodontus francisci (horned shark) has a clustered organization in which variable (V), joining (J), and constant (C) elements are in relatively close linkage (V-J-C). Using a polymerase chain reaction-based approach on a light chain peptide sequence from the holocephalan, Hydrolagus colliei (spotted ratfish), it was possible to isolate members of a second light chain gene family. A probe to this light chain (type II) detects homologs in two orders of elasmobranchs, Heterodontus, a galeomorph and Raja erinacea (little skate), a batoid, suggesting that this light chain type may be present throughout the cartilaginous fishes. In all cases, V, J, and C regions of the type II gene are arranged in closely linked clusters typical of all known Ig genes in cartilaginous fishes. All representatives of this type II gene family are joined in the germline. A third (kappa-like) light chain type from Heterodontus is described. These findings establish that a degree of light chain class complexity comparable to that of the mammals is present in the most phylogenetically distant extant jawed vertebrates and that the phenomenon of germline-joined (pre-rearranged) genes, described originally in the heavy chain genes of cartilaginous fishes, extends to light chain genes.     

Description of the adult skeleton and developmental osteology of the hyperossified horned frog,Ceratophrys cornuta (Anura: Leptodactylidae)

The adult skeleton and tadpole chondrocranium of the leptodcatylid frog, Ceratophrys cornuta (Ceratophryinae), are described in detail, including the ontogenetic development of the chondrocanium and the ossification sequence of the skeleton. The chondrocranium of the carnivorous larvae is unique in lacking a frontoparietal fontanelle and possessing a complete dorsal roof of cartilage. Furthermore, the chondrocranium is extremely robust, particularly those elements involved in the feeding mechanism; these include large palatoquadrate cartilages, stout Meckel's, supra- and infrarostral cartilages, and short, wide, cornua trabeculae. The chondrocranium of C. cornuta resembles that described for Ceratophrys cranwelli, but differs from the chondrocrania reported for the species of Lepidobatrachus. The large adult skull is hyperossified; most elements are fused into a single unit, and nearly all dermal elements are ornamented, casqued, and co-ossified. Calcification is present in nearly every cartilaginous element of the skeleton in larger (older) adults. Several osteological characters previously used in ceratophryine systematics, such as the otic ramus of the squamosal and the columella, are reassessed. Contrary to previous reports, the ossified, dorsal dermal shield above the vertebral column in many ceratophryine anurans is absent in C. cornuta. With few exceptions, the ossification sequence relative to metamorphosis is consistent with those that are known for other anurans. The squamosal arises from three distinct centers of ossification, including an otic element. The frontoparietal arises from two centers of ossification that fuse early in development. A robust postorbital arch is formed primarily by the otic flange of the frontoparietal, which articulates laterally with the medial border of the otic ramus of the squamosal. Changes in the timing of development, or heterochrony, are involved with the evolution of the unusual skull and skeleton of ceratophryine frogs. J Morphol 232:169–206, 1997. © 1997 Wiley-Liss, Inc.     

Cytogenetic mapping of immunoglobulin heavy chain genes in Antarctic fish

The chromosomal location of the IgH locus has been analyzed in several bony fish of the Antarctic perciform group Notothenioidei. Two IgH probes were prepared from the species Trematomus bernacchii (family Nototheniidae, tribe Trematominae) and mapped onto the chromosomes of ten species belonging to the same genus (Trematomus) and in two outgroups, through one-color and two-color FISH. A single location of the IgH locus was found in the majority of the species examined, including the outgroups, whereas in four of them the IgH genes splited to two chromosomal loci. RT-PCR experiments revealed the presence of three allelic sequences in T. newnesi, a species in which the IgH genes were organized in two chromosomal loci. Possible pathways leading to IgH genes duplication during the diversification of trematomine fishes were inferred from the analysis of the FISH patterns in a phylogenetic context. The present work provides the first comprehensive picture of IgH genes organization at chromosomal level in a bony fish group.     

Cloning of a neoteleost (Oreochromis mossambicus) pro-opiomelanocortin (POMC) cDNA reveals a deletion of the γ-melanotropin region and most of the joining peptide region: implications for POMC processing

A signature feature of tetrapod pro-opiomelanocortin (POMC) is the presence of three melantropin (MSH) coding regions (α-MSH, β-MSH, γ-MSH). The MSH duplication events occurred early during the radiation of the jawed vertebrates well over 400 million years ago. However, in at least one order of modern bony fish (subdivision Teleostei; order Salmoniformes; i.e. salmon and trout) the γ-MSH sequence has been deleted from POMC. To determine whether the γ-MSH deletion has occurred in other teleost orders, a POMC cDNA was cloned from the pituitary of the neoteleost Oreochromis mossambicus (order Perciformes). In O. mossambicus POMC, the deletion is more extensive and includes the γ-MSH sequence and most of the joining peptide region. Because the salmoniform and perciform teleosts do not share a direct common ancestor, the γ-MSH deletion event must have occurred early in the evolution of the neoteleost fishes. The post-translational processing of O. mossambicus POMC occurs despite the fact that the proteolytic recognition sequence, (R/K)-X_n-(R/K) where n can be 0, 2, 4, or 6, a common feature in mammalian neuropeptide and polypeptide hormone precursors, is not present at several cleavage sites in O. mossambicus POMC. These observations would indicate that either the prohormone convertases in teleost fish use distinct recognition sequences or vertebrate prohormone convertases are capable of recognizing a greater number of primary sequence motifs around proteolytic cleavage sites.     

Ontogenetic evidence supporting a relationship between <Emphasis Type="Italic">Brotulotaenia</Emphasis> and <Emphasis Type="Italic">Lamprogrammus</Emphasis> (Ophidiiformes: Ophidiidae) based on the morphology of exterilium and rubaniform larvae

Analysis of the Dana collection of larval fishes yielded 36 exterilium larvae and 17 rubaniform larvae, referable to the Ophidiidae. Both larval types reach large sizes before transformation and are characterized by an exterilium gut, although it is less strongly expressed in rubaniform larvae. Both have early-forming, elongate, descending processes of the coracoid that serve to support the trailing intestines. Both have a greatly reduced pelvic girdle attached to a stalklike cartilaginous structure, resulting in a pelvic fin origin well posterior to the cleithral symphysis, a position that is without precedent in the family Ophidiidae. Both of these larval types also strongly display an anterior to posterior developmental sequence, lose the pelvic fin rays at transformation, and have extraordinarily elongate proximal radials supporting their dorsal and anal fins and modified proximal radials supporting the anterior dorsal fin rays. After examination of these larvae and reference to 5 previously described exterilium larvae and 1 previously described rubaniform larva, we conclude that they belong to Lamprogrammus (three species) and Brotulotaenia (four species), respectively. The most recent classification of the Ophidiidae places Brotulotaenia in the monotypic subfamily Brotulotaeniinae, and Lamprogrammus in the subfamily Neobythitinae along with 37 other genera. The latter subfamily is an unwieldy assemblage for which monophyly has never been established. Ontogenetic evidence suggests a closer relationship between Brotulotaenia and Lamprogrammus, and the most economical reorganization of the ophidiids would involve incorporating the latter genus into the Brotulotaeniinae.     

Temperature-dependent energy allocation to growth in Antarctic and boreal eelpout (Zoarcidae)

Antarctic fishes display slower annual growth rates than congeneric species from temperate zones. For an analysis of growth in relation to energy turnover, body composition was analysed in two benthic fish species to establish a whole animal energy budget. The Antarctic eelpout, Pachycara brachycephalum, was maintained at 0, 2, 4 and 6°C and the boreal eelpout, Zoarces viviparus at 4, 6, 12 and 18°C. At maximum food supply the weight gain was highest for P. brachycephalum at 4°C. Routine metabolic rate in acclimated Antarctic eelpouts did not differ between temperatures, whereas in Z. viviparus maximized growth benefited from a reduction of metabolic energy demands at 12°C. The lipid content of liver declined with increasing temperature in both species. The thermal window for growth is based on food conversion efficiency and the level of metabolic energy demand and is limited according to the level of aerobic scope available between pejus temperatures.     

The spinal cord supports of vertebrae in the crown‐group salamanders (Caudata,Urodela)

The development of spinal cord supports (bony thickenings which extend into the vertebral canal of vertebrae) in primitive (Salamandrella keyserlingii) and derived (Lissotriton vulgaris) salamanders were described. The spinal cord supports develop as the protuberances of periostal bone of the neural arches in the anteroproximal part of the septal collagenous fibers which connect a transverse myoseptum with the notochord and spinal cord, in the septal bundle inside the vertebral canal. Spinal cord supports were also found in some teleostean (Salmo salar, Oncorhynchus mykiss) and dipnoan (Protopterus sp.) fishes. The absence of the spinal cord supports in vertebrates with cartilaginous vertebrae (lampreys, chondrichthyan, and chondrostean fishes) corresponds to the fact that the spinal cord supports are bone structures. The absence of the spinal cord supports in frogs correlates with the lack of the well developed septal bundles inside the vertebral canal. The spinal cord supports are, presumably, a synapomorphic character for salamanders which originated independently of those observed in teleostean and dipnoan fishes. J. Morphol. 2012. © 2012 Wiley Periodicals, Inc.     

Evolution of electrosensory ampullary organs: conservation of Eya4 expression during lateral line development in jawed vertebrates

The lateral line system of fishes and amphibians comprises two ancient sensory systems: mechanoreception and electroreception. Electroreception is found in all major vertebrate groups (i.e. jawless fishes, cartilaginous fishes, and bony fishes); however, it was lost in several groups including anuran amphibians (frogs) and amniotes (reptiles, birds, and mammals), as well as in the lineage leading to the neopterygian clade of bony fishes (bowfins, gars, and teleosts). Electroreception is mediated by modified “hair cells,” which are collected in ampullary organs that flank lines of mechanosensory hair cell containing neuromasts. In the axolotl (a urodele amphibian), grafting and ablation studies have shown a lateral line placode origin for both mechanosensory neuromasts and electrosensory ampullary organs (and the neurons that innervate them). However, little is known at the molecular level about the development of the amphibian lateral line system in general and electrosensory ampullary organs in particular. Previously, we identified Eya4 as a marker for lateral line (and otic) placodes, neuromasts, and ampullary organs in a shark (a cartilaginous fish) and a paddlefish (a basal ray‐finned fish). Here, we show that Eya4 is similarly expressed during otic and lateral line placode development in the axolotl (a representative of the lobe‐finned fish clade). Furthermore, Eya4 expression is specifically restricted to hair cells in both neuromasts and ampullary organs, as identified by coexpression with the calcium‐buffering protein Parvalbumin3. As well as identifying new molecular markers for amphibian mechanosensory and electrosensory hair cells, these data demonstrate that Eya4 is a conserved marker for lateral line placodes and their derivatives in all jawed vertebrates.     

The composition of the caudal skeleton of teleosts (Actinopterygil: Osteichthyes)

The diural caudal skeleton of teleostean actinopterygians develops phylogeneticaily and ontogenetically from a polyural skeleton. The reduction of the polyural anlage to four, three, two or fewer centra in the adult caudal skeleton takes different pathways in different genera (e.g. compare Elops and Albula) and groups of teleosts. As a result, ural centra are not homologous throughout the teleosts. By numbering the ural centra in a homocercal tail in polyural fashion, one can demonstrate these and the following differences. The ventral elements (hypurals) always occur in sequential series, whereas the dorsal elements (epurals and uroneurals) may alter like the ural centra. The number of epurals, five or four in fossil primitive teleosts, is reduced in other primitive and advanced teleosts, but the same epurals are not always lost. The number of uroneurals, seven in fossil teleosts, is reduced in living teleosts, but it has not been demonstrated that the first uroneural is always derived from the neural arch of the same ural centrum. The landmark in the homocercal tail is the preural centrum I which can be identified by (1) bifurcation of the caudal artery and vein in its ventral element, the parhypural, (2) its position directly caudal to the preural centrum (PU2) which supports the lowermost principal caudal ray with its haemal spine, (3) carrying the third hypaxial element ventral to the course of arteria and vena pinnalis, and (4) by carrying the first haemal spine (parhypural) below the dorsal end of the ventral cartilage plate. The study of the development of the vertebral column reveals that teleosts have different patterns of centrum formation. A vertebral centrum is a complete or partial ring of mineralized, cartilaginous or bony material surrounding at least the lateral sides of the notochord. A vertebral centrum may be formed by arcocentrum alone, or arcocentral arcualia and chordacentrum, or arco-, chorda- and autocentrum, or arcocentral arcualia and autocentrum. This preliminary research demonstrates that a detailed ontogenetic interpretation of the vertebral centra and of the caudal skeleton of different teleosts may be useful tools for further interpretations of teleostean interrelationships.     

Trematode larvae in snails of Lake Glubokoe

In the Augusts of 1984 and 1985, 6 species of snails in Lake Glubokoe were investigated: Viviparus viviparus (Linne, 1758), Lymnaea ovata (Draparnaud, 1805), L. stagnalis (Linne, 1758), L. corvus (Gmelin, 1791), Planorbis planorbis (Linne, 1758), and Planorbarius corneus (Linne, 1758), which were found to be infected by 9 species of trematode larvae. V. viviparus showed the highest rate of infection — 48.15% ± 6.8. The larvae of trematodes belonging to the families Echinostomatidae and Plagiorchidae predominate in the snails of the lake.