Ontogeny and homology of the claustra in otophysan Ostariophysi (Teleostei)

We studied the ontogeny of the claustrum comparatively in representatives of all otophysan subgroups. The claustrum of cypriniforms has a cartilaginous precursor, the claustral cartilage, which subsequently ossifies perichondrally at its anterior face and develops an extensive lamina of membrane bone. The membrane bone component of the claustrum and its close association with the atrium sinus imparis, a perilymphatic space of the Weberian apparatus, are both synapomorphies of cypriniforms. The characiform claustrum is not preformed in cartilage and originates as a membrane bone ossification, a putative synapomorphy of that taxon. Among siluriforms, the claustrum is present only in more basal groups and originates as an elongate cartilage that ossifies in a characteristic ventrodorsal direction, possibly a synapomorphy of catfishes. Gymnotiforms lack the claustral cartilage and claustrum. We review all previous hypothesis of claustrum homology in light of the above findings and conclude that the most plausible hypothesis is the one originally proposed by Bloch ([1900] Jen Z Naturw 34:1-64) that claustra are homologs of the supradorsals of the first vertebra.     

The morphology of the club glands on the dorsal fin of mature male shannies, Lipophvys pholis (L.) (Blenniidae: Teleostei)

The pelvic, pectoral, anal and dorsal fins of mature male, female and immature male Lipophrys pholis (L.) were examined by light microscopy for the presence of club glands. All fins except the dorsal showed a highly stratified epidermis and a thick cuticle. Club glands were present on the dorsal fin of mature male fisH but only during the breeding season. The development and decline of the club glands corresponds to the period of gonadal build-up and spawnout. Each club gland comprises several thousand bundles ofcolumnar cells. The columnar cells surround acentral pore which opens to the outside through a layer of Malpighian cells. The substance produced by the gland includes mucopolysacchdride. The function of the secretion is unknown and is discussed in relation to studies on similar glands in several Mediterranean blenniids.     

The median‐fin skeleton of the Eastern Atlantic and Mediterranean clingfishes Lepadogaster lepadogaster (Bonnaterre) and Gouania wildenowi (Risso) (Teleostei: Gobiesocidae)

Previous research on the osteology of the Gobiesocidae focused mostly on the neurocranium and the thoracic sucking disc (formed by the paired‐fin girdles). Little attention has been paid to the skeleton of the median fins. The dorsal‐ and anal‐fin skeleton of Lepadogaster lepadogaster and other gobiesocids (excluding Alabes, which lacks these fins) are characterized by the absence of spines, branched fin‐rays, and middle radials. In gobiesocids, the distal radials never ossify and consist of elastic hyaline‐cell cartilage. Gouania wildenowi is unique among gobiesocids in having further reductions of the dorsal‐ and anal‐fin skeleton, including a notable decrease in the size of the proximal‐middle radials in an anterior–posterior direction. Unlike L. lepadogaster, which exhibits a one‐to‐one relationship between the dorsal‐ and anal‐fin rays and proximal‐middle radials, G. wildenowi has a higher number of proximal‐middle radials than distal radial cartilages and fin rays in the dorsal and anal fins. In G. wildenowi, the dorsal‐ and anal‐fin rays do not articulate with the distal tip of the proximal‐middle radials but are instead positioned between proximal‐middle radials, which is unusual for teleosts. Previously unrecognized dorsal and ventral pads of elastic hyaline‐cell cartilage are also present in the caudal skeleton of L. lepadogaster, G. wildenowi, and all other gobiesocids examined. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.     

Ontogeny,variation, and homology in Salvelinus alpinus caudal skeleton (Teleostei: Salmonidae)

The ontogeny of the caudal skeleton in the Arctic charr, Salvelinus alpinus was examined using an extensive series of cleared and stained specimens. We demonstrate the presence of skeletal components never reported previously within the Salmonidae. In contrast to the generalized condition for salmonids, seven hypurals (instead of six), and four uroneurals (instead of three) have been found in some specimens. Variation in the number and condition of epurals is documented. New hypotheses are proposed concerning (1) relationships among centra and their associated elements, (2) phylogenetic distribution of caudal characters within the Salmonidae, and (3) homology of caudal components. Using the published phylogenetic hypotheses, we provide evidence, that a seventh hypural and a fourth uroneural are taxic atavism in salmonids. The development of the salmonid homocercal fin is discussed in the light of a polyural scheme based on evidences of a one‐to‐one relationship among ural centra and their associated elements. J. Morphol., 2010. © 2009 Wiley‐Liss, Inc.     

Ontogeny and homology of the basipterygoid articulation in Pantodon buchholzi (Teleostei: Osteoglossomorpha)

The basipterygoid articulation, an articular connection between the base of the braincase and the palatoquadrate, is widespread among gnathostome vertebrates. However, among living teleosts it is present only in the osteoglossomorphs Arapaima , Heterotis , Scleropages , Osteoglossum and Pantodon . Study of the development of the hyopalatine arch and the basipterygoid articulation in Pantodon buchholzi based on an ontogenetic series of cleared and double stained specimens yielded the following results: the symplectic process of the hyosymplectic cartilage never develops and the symplectic is absent; the pars hyomandibularis fuses with the palatoquadrate; the dermopalatine and ectopterygoid originate as separate bones, but fuse subsequently; the basal process is first visible on the pars metapterygoidea of the palatoquadrate at 7.0 mm standard length (SL); at 11.5 mm SL the basipterygoid process appears on the parasphenoid and contacts the basal process, establishing the basipterygoid articulation; the endopterygoid is initially not involved in the articulation, but during subsequent development enlarges and eventually forms an articular groove for the reception of the basipterygoid process of the parasphenoid; the distal tip of the basal process of the metapterygoid, however, still forms the caudolateral part of the articular groove in the adult. We discuss previous hypotheses about the homology of the basipterygoid articulation of osteoglossoids in light of these findings. Based on the numerous shared similarities and its occurrence in all major actinopterygian lineages, we argue that the basipterygoid articulation in osteoglossoids is homologous to that in non teleostean actinopterygians and represents a plesiomorphic character state at the level of Osteoglossomorpha.  © 2005 The Linnean Society of London, Zoological Journal of the Linnean Society , 2005, 144 , 1−13.     

Ontogeny of the catfish pectoral-fin spine (Teleostei: Siluriformes)

The characteristic and morphologically variable pectoral-fin spine of catfishes (order Siluriformes) has been well-investigated based on later developmental stages (juveniles and adults) but information on the earliest life stages are lacking. Here, we document the ontogeny of pectoral-fin spines in four siluroid (Ictalurus punctatus, Noturus gyrinus, Silurus glanis and Akysis vespa) and two loricarioid catfishes (Corydoras panda and Ancistrus sp.). To further our understanding of pectoral-fin spine development, we also examined adult and juvenile specimens representing 41 of the currently 43 recognized families of catfishes. Development of the pectoral-fin spine is similar in all catfishes and resembles the development of a typical soft fin ray. Fusion between hemitrichia of the anteriormost lepidotrichium occurs proximally first, forming the spine proper, with growth of the spine occurring through the subsequent fusion of developing distal hemitrichial segments that comprise the spurious ray. The variation of pectoral-fin spine morphology observed is largely attributed to the presence/absence of five traits, which either develop as part of the hemitrichial segments that are added to the distal tip of the spine during growth (distal rami, anterior/posterior serrae) or develop independent of these segments (denticuli and odontodes).     

First record of saddleback syndrome in wild parrotfish Sparisoma cretense (L., 1758) (Perciformes, Scaridae)

The saddleback syndrome is recorded for the first time in a wild fish population of the Mediterranean Sea. The deformed specimen belongs to Sparisoma cretense and presents the typical saddleback phenotype of missing spines in the dorsal fin.     

The dorsal groove and associated structures on the head of the sucking loach, Gyrinocheilus aymonieri (Cypriniformes)

A prominent transverse groove is present on the snout of the adult sucking loach, Gyrinocheilus aymonieri . It is absent in juveniles. The groove is formed by fibrous thickenings of the dermis that create skin folds at its anterior and posterior margins. It accommodates movement of the joint between the maxillae and the neurocranium. The anterior fibrous thickening also provides anchorage for fibrous strands that partition dermal mucochondroid in the upper lip of the oral sucker into distinct segments. This structure forms a buffer that protects the delicate premaxillary bones when fish probe the substrate for food.     

A specimen of Salmo trutta (Pisces: Salmonidae) possessing an additional dorsal fin

A specimen of brown trout, Salmo trutta , with a supernumerary dorsal fin located just posterior to the nape is documented from the Yarra River, Victoria, Australia.     

Correlated evolution of body and fin morphology in the cichlid fishes

Body and fin shapes are chief determinants of swimming performance in fishes. Different configurations of body and fin shapes can suit different locomotor specializations. The success of any configuration is dependent upon the hydrodynamic interactions between body and fins. Despite the importance of body–fin interactions for swimming, there are few data indicating whether body and fin configurations evolve in concert, or whether these structures vary independently. The cichlid fishes are a diverse family whose well‐studied phylogenetic relationships make them ideal for the study of macroevolution of ecomorphology. This study measured body, and caudal and median fin morphology from radiographs of 131 cichlid genera, using morphometrics and phylogenetic comparative methods to determine whether these traits exhibit correlated evolution. Partial least squares canonical analysis revealed that body, caudal fin, dorsal fin, and anal fin shapes all exhibited strong correlated evolution consistent with locomotor ecomorphology. Major patterns included the evolution of deep body profiles with long fins, suggestive of maneuvering specialization; and the evolution of narrow, elongate caudal peduncles with concave tails, a combination that characterizes economical cruisers. These results demonstrate that body shape evolution does not occur independently of other traits, but among a suite of other morphological changes that augment locomotor specialization.     

Ontogeny of Double Cones in the Retina of Perch Fry (Perca fluviatilis,Teleostei)

The formation of double cones in the retina of fry of Perca fluviatilis has been investigated by light and electron microscopy. The retina of newly hatched fry is provided with single cones and rods, single cones being the predominant receptor type. Double cones are seen for the first time 22 days after hatching. Mitoses are observed in the periphery of the retina, but are also seen in more central parts of the retina containing differentiated receptors and a cone mosaic. The fate of the cells resulting from the centrally located mitoses is not known. No signs of longitudinal fission of differentiated single cones are seen. It is suggested that double cones in the retina of perch fry arise by fusion of single cones which associate closely and develop subsurface cisterns coextensive with the region of intimate contact in the ellipsoid. During the first few weeks after hatching, there is a gradual shift in arrangement of the cones. In the newly hatched fry, the single cones are arranged in rows. When double cones are first seen, square-pattern units appear, built up from four double cones and a single cone.     

The Ontogeny of Neonesidea oligodentata (Bairdioidea, Ostracoda, Crustacea)

This is the first detailed ontogenetic study of the appendages and carapace of a bairdioidean ostracod. This paper uses the development of the appendages and changes in the pore systems of the carapace through ontogeny to help determine the relationship between the Bairdioidea and other podocope groups. Neonesidea oligodentata has eight post-embryonic stages: one fewer than the Cypridoidea, Cytheroidea and Darwinuloidea. The first instar of N. oligodentata resembles that of the second instar of the Cypridoidea and Cytheroidea in terms of appendages, and it is postulated that there is an additional instar stage of N. oligodentata that molts within the egg. The general sequence of appearance of the limbs from instar A-7 onwards is similar to that of the Cypridoidea and Cytheroidea, but different from that of the Darwinuloidea. Like the Cypridoidea and Cytheroidea, N. oligodentata has a gap in its ontogenetic development during instar A-6, where no new Anlage is added. Pore system analysis of A-7 instars suggests that the Bairdioidea may be more closely related to the Cypridoidea than to the Cytheroidea.     

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.     

Leis' conundrum: homology of the clavus of the ocean sunfishes. 2. Ontogeny of the median fins and axial skeleton of Ranzania laevis (Teleostei, Tetraodontiformes, Molidae)

One of the most conspicuous characters of the ocean sunfishes, family Molidae, is the punctuation of the body by a deep, abbreviated, caudal fin-like structure extending vertically between the posterior ends of the dorsal and anal fins, termed the clavus by Fraser Brunner. Homology of the clavus has been a matter of debate since the first studies on molid anatomy in the early 1800s. Two hypotheses have been proposed: 1) It is a highly modified caudal fin; 2) It is formed by highly modified elements of the dorsal and anal fins. To resolve this homology issue, we studied the ontogeny of the molid vertebral column and median fins and compared it to that of a less morphologically derived gymnodont (see Part 1 of this study), a member of the family Tetraodontidae. We show that in molids the chorda never flexes during development, that the claval rays form from the posterior ends of the dorsal and anal fins toward the middle, thus closing the gap inward, and that elements of the molid clavus have an identical development and composition as the proximal-middle and distal radials of the regular dorsal and anal fins. We thus conclude that the molid clavus is unequivocally formed by modified elements of the dorsal and anal fin and that the caudal fin is lost in molids.     

Anal‐fin ray morphology indicates sexual maturity in Brevimyrus niger (Teleostei,Mormyridae)

This osteological survey of 249 specimens of Brevimyrus niger ranging in size from 44 to 137 mm standard length (L_S) demonstrated that developmental changes in anal‐fin morphology can serve as a predictor of sexual maturity in this species. Anal‐fin ray bases begin to expand when fish reach c. 90 mm L_S at which size and above there were roughly equal numbers of individuals observed with expanded and unmodified anal‐fin bases, reflecting a 1:1 sex ratio.     

The dorsal fin engine of the seahorse (Hippocampus sp.)

The muscles, fin ray joints, and supporting structures underlying the dorsal fin are described for two seahorse species: Hippocampus zosterae and Hippocampus erectus. A fan-shaped array of cartilaginous bones, the pterigiophores, form the internal supporting structure of the dorsal fin. Each pterigiophore is composed of a proximal radial that extends from a vertebra to the dorsal side of the animal, where it fuses to a middle radial. The middle radials fuse with each other to form a dorsal ridge upon which sit the spheroidal distal radials. Each distal radial articulates with a fin ray on its dorsal side and is attached to the dorsal ridge on its ventral side by a material that has been histologically identified as elastic cartilage. Together these connections form a two-axis joint that permits elevation, depression, and inclination of the ray. Each fin ray is actuated by two bilateral pairs of muscles, an anterior pair of inclinators, and a posterior pair of depressors. The anteriormost fin ray is actuated by three bilateral pair of muscles, the inclinators, the depressors, and a pair of elevator muscles that are positioned anterior to the inclinators. Preliminary examinations of the ray joints of the pectoral and anal fins of adult H. zostera and the pectoral fins of newborn H. erectus revealed structures similar to that seen in the dorsal fins. To further explore the structure and function of the dorsal fin gross dissections and simple functional tests were performed on H. erectus and H. barbouri and behavioral observations were made of all three species plus Hippocampus kuda.