Histochemical study of jaw muscle fibers in the American alligator (Alligator mississippiensis)

The ontogenetic development of caudal vertebrae and associated skeletal elements of salmonids provides information about sequence of ossification and origin of bones that can be considered as a model for other teleosts. The ossification of elements forming the caudal skeleton follows the same sequence, independent of size and age at first appearance. Dermal bones like principal caudal rays ossify earlier than chondral bones; among dermal bones, the middle principal caudal rays ossify before the ventral and dorsal ones. Among chondral bones, the ventral hypural 1 and parhypural ossify first, followed by hypural 2 and by the ventral spine of preural centrum 2. The ossification of the dorsal chondral elements starts later than that of ventral ones. Three elements participate in the formation of a caudal vertebra: paired basidorsal and basiventral arcocentra, chordacentrum, and autocentrum; appearance of cartilaginous arcocentra precedes that of the mineralized basiventral chordacentrum, and that of the perichordal ossification of the autocentrum. Each ural centrum is mainly formed by arcocentral and chordacentrum. The autocentrum is irregularly present or absent. Some ural centra are formed only by a chordacentrum. This pattern of vertebral formation characterizes basal teleosts and primitive extant teleosts such as elopomorphs, osteoglossomorphs, and salmonids. The diural caudal skeleton is redefined as having two independent ural chordacentra plus their arcocentra, or two ural chordacentra plus their autocentra and arococentra, or only two ural chordacentra. A polyural caudal skeleton is identified by more than two ural centra, variably formed as given for the diural condition. The two ural centra of primitive teleosts may result from early fusion of ural centra 1 and 2 and of ural centra 3 and 4, or 3, 4, and 5 (e.g., elopomorphs), respectively. The two centra may corespond to ural centrum 2 and 4 only (e.g., salmonids). Additionally, ural centra 1 and 3 may be lost during the evolution of teleosts. Additional ural centra form late in ontogeny in advanced salmonids, resulting in a secondary polyural caudal skeleton. The hypural, which is a haemal spine of a ural centrum, results by growth and ossification of a single basiventral ural arococentrum and its haemal spine. The proximal part of the hypural always includes part of the ventral ural arcocentrum. The uroneural is a modification of a ural neural arch, which is demonstrated by a cartilaginous precursor. The stegural of salmonids and esocids originates from only one paired cartilaginous dorsal arcocentrum that grows anteriorly by a perichondral basal ossification and an anterodorsal membranous ossification. The true epurals of teleosts are detached neural spines of preural and ural neural arches as shown by developmental series; they are homologous to the neural spines of anterior vertebrae. Free epurals without any indication of connection with the dorsal arococentra are considered herein as an advanced state of the epural. Caudal distal radials originate from the cartilaginous distal portion of neural and haemal spines of preural and ural (epurals and hypurals) vertebrae. Therefore, they result from distal growth of the cartilaginous spines and hypurals. Cartilaginous plates that support rays are the result of modifications of the plates of connective tissue at the posterior end of hypurals (e.g., between hypurals 2 and 3 in salmonids) and first preural haemal spines, or from the distal growth of cartilaginous spines (e.g., epural plates in Thymallus). Among salmonids, conditions of the caudal skeleton such as the progressive loss of cartilaginous portions of the arcocentra, the progressive fusion between the perichondral ossification of arcocentra and autocentra, the broadening of the neural spines, the enlargement and interdigitation of the stegural, and other features provide evidence that Prosopium and Thymallus are the most primitive, and that Oncorhynchus and Salmo are the most advanced salmonids respectively. This interpretation supports the current hypothesis of phylogenetic relationships of salmonids. © 1992 Wiley-Liss, Inc.     

Development of the vertebral column and caudal complex in a flyingfish,Parexocoetus mento mento (Teleostei: Exocoetidae)

The developmental pattern of the vertebral column and caudal complex in juvenile (16.9 mm SL) to adult (112.2 mm SL)Parexocoetus mento mento is described Juvenile external caudal morphology was similar to the adult condition, although juveniles exhibited various internal ontogenetic changes. Osteological develoment was almost completed at 60–69 mm SL. Complete ossification of the vertebral column and caudal complex appeared to be the optimal condition giving strength for flight. Loss of perforations in the centra, neural and haemal arches may be consistent with the rigid and straightened body position during take-off. Some ontogenetic changes in the caudal complex were related to functional aspects. Ankylosis of the NPU2 spur to the uroneural notch, fusion of hypurals 3+4 and 5 and the elongated hypural 1+2 (lower hypural) were linked to the acquisition of stability and strength in the caudal complex.     

Osteological development of the lumpfish,inimicus japonicus (pisces: Synanceiidae)

The osteological development of the synanceiidInimicus japonicus, was described on the basis of five larvae and four juveniles (4.2–10.1 mm BL) reared in the laboratory, and two wild adult specimens. All bones, except for the basisphenoid, were formed in all larvae and juveniles, but fusions between the uppermost actinost and scapula, upper caudal plate and urostyle, and third preural centrum and hemal spine were not completed by 10.1 mm BL. Following comparison with the adult condition, a rod-like ossified bone without a tooth plate on the upper branchial arch of larvae and juveniles was considered homologous with the second pharyngobranchial. The number of epurals and length of the neural spine on the second preural centrum varied (unrelated to growth) and it is inferred thatJ. japonicus shows intraspecific variations in these bones.     

Phylogeny of the flyingfish family Exocoetidae (Teleostei, Beloniformes)

The phylogeny of the flyingfish family Exocoetidae is studied cladistically, using 41 morphological characters encompassing early life history, and external and internal features. The monophyly of the family is supported by 10 synapomorphies. Within the family,Oxyporhamphus is the sister group to all other genera, the monophyly of the latter being defined by 10 synapomorphies.Fodiator is the sister group of genera characterized by the presence of chin barbels in juveniles.Parexocoetus is the sister group ofExocoetus, Cypselurus, Prognichthys andHirundichthys, the latter being defined by four synapomorphies. In the latter group,Exocoetus is the sister group of the other three genera. The phylogeny of the Exocoetidae is characterized by the stepwise upgrading of gliding capability, with sequential modifications of the caudal, pectoral and pelvic fins. The subfamily Oxyporhamphinae is resurrected.     

Neolumpenus unocellatus,a new genus and species of stichaeid fish from Japan

Neolumpenus unocellatus gen. et sp. nov., a stichaeid fish (subfamily Lumpeninae,sensu Makushok, 1958) is described on the basis of a single specimen found in the stomach of the Pacific cod,Gadus macrocephalus Tilesius, caught off Akkeshi, Hokkaido, Japan. The new genus and species is distinguished from all other lumpenines in having the following combination of characters: 1) 51 dorsal spines, 33 anal fin rays, 57 total vertebrae; 2) broad pelvic fin with deeply-branched soft rays; 3) lower rays of pectoral fin branched and not prolonged backward; 4) prevomerine and palatine teeth present; 5) pungent spines present in pelvic and anal fins; 6) upper lip fused to snout anteriorly; 7) gill openings not extending forward beyond a vertical through posterior margin of eye; 8) minimal (fifth) hypural present; 9) first interneural spine inserted between first and second neural spines; 10) extremely large cephalic sensory pores present; 11) high, steep snout; 12) ocellus on dorsal base of caudal fin.     

Étude de Pseudanogmius maiseyi gen. et sp. nov., poisson marin (Teleostei, Tselfatiiformes) du Crétacé supérieur du Kansas (États-Unis)

The osteology of Pseudanogmius maiseyi gen. and sp. nov., a marine teleost of the Upper Cretaceous of Kansas, is studied. This fish belongs to the order Tselfatiiformes and more particularly to the group with a more or less flat skull roof and with large, quadrangular and joined parietals. Pseudanogmius maiseyi, formerly named Anogmius sp. by Hay (1903), differs from Bananogmius and the other genera known in the order by three autapomorphies: an elongated and very narrow vomer, a peculiar relief of the toothed part of the parasphenoid, and transverse processes on the caudal vertebrae. Within the order, it shows a few evolved characters, such as the loss of the preural 1 hemal arch and of the sixth autogenous hypural and by the shortening of the preural 1 neural spine.     

Leis' conundrum: homology of the clavus of the ocean sunfishes. 1. Ontogeny of the median fins and axial skeleton of Monotrete leiurus (Teleostei, Tetraodontiformes, Tetraodontidae)

We describe the ontogeny of the axial skeleton and median fins of the Southeast Asian freshwater puffer Monotrete leiurus, based on a reared developmental series. Most elements of the axial skeleton in M. leiurus arise in membrane bone. Only the base of the anterior three neural arches, the base of the hemal arches of the third preural centrum, the neural and hemal arches and spines of the second preural centrum, the parhypural, the two hypural plates, and the single epural are preformed in cartilage. In contrast to most teleosts, the proximal-middle radials of the dorsal and anal fins are upright and symmetrical and their distal tips coalesce during development to form a deep band of cartilage, from which the spherical distal radials are spatially separated.     

A new species, Trichiurus australis (Perciformes: Trichiuridae), from Australia

Trichiurus australis, a new trichiurid fish, is described on the basis of four specimens collected off Burnett River mouth, Pialba and Thursday Island, Queensland, Australia. The new species strongly resembles Trichiurus brevis Wang and You, 1992 (distributed in the South China Sea), T. russelli Dutt and Thankam, 1967 (the northwestern Bay of Bengal and the northern Gulf of Thailand), and T. nickolensis Burhanuddin and Iwatsuki, 2003 (northwestern Australia) in having the highest point of the supraoccipital crest situated directly above the posterior margin of the eye and being relatively small in size (less than ca. 700mm in total length: TL). It differs from those three species in having spinescent gill rakers almost with 2 equally long cusps [vs. (1, rarely 2 but 1 of them clearly shorter than another)], posterior caudal peduncle vertebrae bearing neural spines (vs. neural spines absent), longer caudal peduncle length (mean 16% TL vs. 6% in T. brevis, 8% in T. nickolensis, and 8% in T. russelli), and shorter precaudal length (83% vs. 93%, 91%, and 91%), preanal length (26% vs. 33%, 31%, and 35%), and head length (9% vs. 12%, 11%, and 13%). We have tentatively classified this new species under the Trichiurus russelli complex because the foregoing diagnostic characters are identical to this species complex except for the presence of neural spines in the posterior caudal vertebrae.     

Description and familial allocation of the African fluvial genus <Emphasis Type="Italic">Teleogramma</Emphasis> to the Cichlidae

 The external morphology, osteology, and myology of the African fluvial genus Teleogramma are described, and its familial allocation is discussed. Teleogramma is included in the family Cichlidae by loss of a major structural association between adductor mandibulae sections 2 and w, and by having an insertion of a large ventral division of adductor mandibulae section 2 onto the anguloarticular, expanded head of the fourth epibranchial, transversus dorsalis subdivided into four parts, functionally decoupled premaxillae and maxillae, the stomach's extendible blind pouch, the left-hand exit to the anterior intestine, the first intestinal loop at the left side, two epurals, seven branched rays on each upper and lower caudal fin lobe, free first uroneural from a united element of first preural and ural vertebra, and third preural vertebra fused with its haemal spine. Seven synapomorphies supporting the monophyly of Teleogramma are indicated, including the absence of or very low supraoccipital crest, the presence of a nostril tube, nonextended supraoccipital anteriorly, absence of extensive cartilaginous cap on the anterior border of the second epibranchial, presence of a beaklike projection on the cleithrum, caudal branched slip of epaxialis that inserts onto the upper two or three branched rays on the upper lobe of the caudal fin, and flexor dorsalis superior, which inserts onto the lower four unbranched rays on the upper lobe of the caudal fin. Received: September 12, 2001 / Revised: December 17, 2001 / Accepted: December 28, 2001     

Orthogonikleithrus leichi n. gen., n. sp. (pisces: teleostei) from the late jurassic of Germany

Orthogonikleithrus leichi n. gen and n. sp. from the Late Jurassic of Zandt, W-Germany resemblesLeptolepides in the supra- and infraorbital sensory canals and in the length of the anterior process of the maxilla, andAscalabos in the massive aspect of the premaxilla. The caudal skeleton has some similarities with that ofLeptolepides (e. g. the broadening of the neural and haemal spines of the last caudal vertebrae, length of uroneurals 1 and 2), but also with that ofAnaethalion (in the neural arches above preural centrum 1 and ural centra). According to this combination of features, the fish remains as Elopocephala incertae sedis.     

Kinorhyncha from the stomach of the shrimp Pleoticus muelleri (Bate, 1888) from Comodoro Rivadavia, Argentina

Six kinorhynchs were found in the stomachs of the Argentine red shrimp, Pleoticus mulleri (Bate, 1888) from the Argentine coast of Patagonia. Three new species are described: Condyloderes storchi n. sp., Pycnophyes argentinensis n. sp. and P. neuhausi n. sp. A fourth species, Kinorhynchus anomalus Lang, 1953 was previously known only from the coast of Chile. This is the third known record of kinorhynchs documented as a food source. Condyloderes storchi, n. sp. is the fourth new species in this genus. It is distinguished by its paradorsal cuspidate spines on segments 7 and 9, lateral accessory and ventrolateral spines on segments 3, 6, 7, 10 and 11. P. argentinensis, n. sp. has nearly equal sternal width for segments 3–11 (about 7% of the trunk length), episternal plates with three distinct areas along the anterior margin, mid-sternal plate with even margin, mid-dorsal spinose protrusions along the terminal borders of segments 11 and 12, and lateral terminal spines 176 μm long, about 21% of trunk length. P. neuhausi, n. sp.has a prominent posterior elongation of the tergal plate of segment 3, uneven lateral margins of the mid-sternal plate, a maximum sternal width at segment 3, no mid-dorsal spinose processes and mid-ventral thickenings on segments 10–12.     

A NEW TITANOSAUR FROM WESTERN SÃO PAULO STATE, UPPER CRETACEOUS BAURU GROUP, SOUTH-EAST BRAZIL

Abstract: Material from a new titanosaur from the Bauru Basin (Bauru Group), Brazil is described and compared with well‐known titanosaurs. Adamantisaurus mezzalirai gen. et sp. nov. is based on six articulated anterior caudal vertebrae and two haemapophyses collected from the Adamantina Formation, which is considered to be Campanian–Maastrichtian? in age. Adamantisaurus mezzalirai is characterized by the following combination of characteristics: anterior caudal vertebrae with straight or slightly backwardly‐projecting neural spines with strongly expanded distal ends, stout prespinal lamina, very wide pre‐ and postzygapophyseal articular facets, and concave postzygapophyseal articular facets on anterior caudal vertebrae. Although our cladistic analysis has produced equivocal results, Adamantisaurus mezzalirai shares with DGM ‘Series B’ (Peirópolis titanosaur) and Aeolosaurus the presence of postzygapophyses with concave articular facets, and shares with DGM ‘Series B’ the presence of laterally expanded neural spines and stout prespinal lamina. Additionally, A. mezzalirai shares with DGM ‘Series’ C (other titanosaur from Peirópolis) the presence of short neural spines.     

Redescription of a rare bothid,Asterorhombus bleekeri (Macleay), and description of a new species ofAsterorhombus from northwestern Australia (Teleostei: Pleuronectiformes)

A rare Australian bothid flounder.Asterorhombus bleekeri (Macleay), is redescribed from the holotype and ten additional specimens from the east coast of Qeensland, Gulf of Carpentaria and Rowly Shoal (Western Australia). The species is transferred fromArnoglossus Bleeker toAsterorhombus Tanaka because of the lack of obvious sexual dimorphism in the interorbital width and pectoral fin length, the lack of rostral and orbital spines, the yellow-white blind side body coloration, and the deeply cleft parhypural and hypural plates. The definition ofAsterorhombus was emended as follows: the first dorsal fin ray continuous with or separated from remaining fin rays and gill rakers slender or stubby, with or without serrations.Asterorhombus osculus sp. nov., formerly briefly described in the literature as unidentified species ofEngyprosopon, was described from eight specimens from the northwestern coast of Australia. The new species is most similar toA. bleekeri in lacking sexual dimorphism, and having the caudal skeleton with deep clefts, two or three rows of teeth on the upper jaw and a pair of conspicuous black spots on the caudal fin, in addition to a similar general appearance, but is distinguished from the latter by shorter gill rakers, a very small mouth and feebly ctenoid scales on the ocular side. Both species clearly differed fromA. intermedius andA. fijiensis in having two (or three) rows of teeth on the upper jaws, slender gill rakers without serrations, first dorsal fin ray continuous with the other fin rays, and a pair of conspicuous black spots on the caudal fin.     

Deconstructing an octogenarian misconception reveals the true Corydoras arcuatus Elwin 1938 (Siluriformes: Callichthyidae) and a new Corydoras species from the Amazon basin

After 80 years of misidentifications, the analysis of the holotype of Corydoras arcuatus plus several non-type specimens attributed to this species allowed its recognition and also revealed a new species, both sharing the following diagnostic features: a long, arched, continuous black stripe that runs parallel to the dorsal profile of the body and extends at least from the anterior margin of the first dorsolateral body plate to the posterior portion of caudal peduncle; absence of transverse black bars on caudal fin; infraorbital 2 in contact with sphenotic and compound pterotic. In addition to these features, C. arcuatus can be distinguished from congeners by having the posterior margin of both dorsal and pectoral spines with laminar serrations directed towards their origins. The new species can be additionally distinguished from its congeners by presenting the following combination of features: ventral surface of trunk entirely or partially covered by relatively large and coalescent platelets; absence of spots or blotches on dorsal fin; and posterior margin of both dorsal and pectoral spines with serrations directed towards their tips. Finally, an identification key to all arc-striped species of Corydoras is provided.     

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.     

Validity of the leiognathid fish,Gazza dentex (Valenciennes in Cuvier and Valencinnes, 1835), with designation of a lectotype, and redescription ofG. minuta (Bloch, 1795)

Gazza dentex (Valenciennes in Cuvier and Valenciennes, 1835), having been synonymized withG. minuta (Bloch, 1795), is redescribed as a valid species.Gazza dentex differs fromG. minuta in having deeper body (43.6–51.4% of standard length [SL] vs. 28.3–46.5% of SL), a broad anterodorsal extension of subocular silvery region, in contact with orbit proximally and distally (vs. a long narrow anterodorsal extension, proximal contact only with orbit), scaled area of anterior dorsolateral suface of body not beyond a vertical through posterior tip of sensory canal on temporal (vs. beyond), distance from posterior margin of temporal to anterior tip of dorsolateral scaled area equal to length of 3–5 anterior pored lateral line scales (vs. length of 1–2.5 anterior pored lateral line scales), some dark narrow wavy bands dorsolaterally on body (vs. some dark broad wavy bands above lateral line and a row of dark spots along lateral line), first interneural inserted deeply between first and second neural spines (vs. inserted shallowly), anterior expansion of first interneural narrow, its margin concave (vs. anterior expansion broad, its margin broadly convex), antrorse extension of first interhemal short, deep, acutely pointed (vs. long, moderately deep, pointed) first to fourth hypurals forming 2 plates (first+second and third-fourth hypurals) (vs. a single plate). The lectotype and three paralectotypes are designated forG. dentex, andG. minuta is redescribed.     

Mongolodiaptomus dumonti n. sp., a new freshwater copepod (Calanoida,Diaptomidae) from Thailand

Mongolodiaptomus dumonti n. sp. from several localities in northeast Thailand is described and figured. The new species shares some features with Mongolodiaptomus gladiolus (Shen & Lee), M. calcarus (Shen & Tai) and M. rarus (Reddy, Sanoamuang & Dumont), thus the gladiolus-group is created. However, it stands out in the female, by the extraordinary large postero-laterally spine at left proximal margin of genital somite. In the male, the right caudal ramus has a large tooth and a bilobed knob on ventral side; basis of the right P5 has a distinct, spur-like process on mid-distal surface; the second exopodite-segment of the right P5 has characteristically irregular outer margin, enlarged at proximal 1/3, but narrowed at distal 2/3 and bearing three lateral spines of unequal sizes; the inner margin of basis of the left P5 is fringed with a narrow hyaline lamella and dilated distally in lateral angle.