Rasbora dusonensis, R. tornieri and R. myersi are valid species. Rasbora dusonensis sensu Brittan (1954) is R. tornieri and R. dusonensis sensu Kottelat (1991) is R. myersi. Both R. dusonensis and R. tornieri are members of the R. argyrotaenia group and can be distinguished from congeners in having a broad, dark, sharply-defined midlateral stripe on body extending from opercle to caudal-fin bas...

In this study, we measured the morphometric and histological changes in the cyprinid loach, Misgurnus anguillicaudatus, during the early period of growth. Eyes, yolk length, yolk height, and yolk volume of the larva decreased for 16 days post hatching (DPH) (P<0.05). During 60 DPH (P>0.05), the most anterior extension of the head × the posterior end of the supraoccipital, the most anterior exte...

Pethia longicauda, a new cyprinid fish, is described from Hiranyakeshi River, Krishna drainage, Maharashtra, India. It can be distinguished from congeners based on a combination of characters including: a long caudal peduncle, incomplete lateral line, absence of barbels, upper lip thick and fleshy, distinct lateral fold on snout, 22-24 scales in lateral series, 5-6 lateral-line pored scales, ni...

A nested polymerase chain reaction (PCR) assay was used to detect early stages of Myxobolus cerebralis in caudal and adipose fin samples from rainbow trout (RT). To determine sensitivity, groups of 10 RT were exposed to 2,000 M. cerebralis triactinomyxons/fish for 1 hour at 15 degrees C and subsequently moved to clean recirculating water. Fish were held for 2 and 6 hours and 1, 2, 3, 5, 7, 10, ...

Regeneration of the zebrafish caudal fin following amputation occurs through wound healing, followed by formation of a blastema, which produces cells to replace the lost tissue in the final phase of regenerative outgrowth. We show that ptpn11a-/- ptpn11b-/- zebrafish embryos, lacking functional Shp2, fail to regenerate their caudal fin folds. Rescue experiments indicated that Shp2a has a functi...

Designing a robotic fish is a challenging endeavor due to the non-linear dynamics of underwater environments. In this paper, we present an evolutionary computation approach for designing the caudal fin of a carangiform robotic fish. Evolutionary experiments are performed in a simulated environment utilizing a mathematical model to approximate the hydrodynamic motion of a flexible caudal fin. Wi...

Gliding adaptations in thoracopterid flying fishes represent a remarkable case of convergent evolution of overwater gliding strategy with modern exocoetid flying fishes, but the evolutionary origin of this strategy was poorly known in the thoracopterids because of lack of transitional forms. Until recently, all thoracopterids, from the Late Triassic of Austria and Italy and the Middle Triassic ...

Designing a robotic fish is a challenging endeavor due to the non-linear dynamics of underwater environments. In this paper, we present an evolutionary computation approach for designing the caudal fin of a carangiform robotic fish. Evolutionary experiments are performed in a simulated environment utilizing a mathematical model to approximate the hydrodynamic motion of a flexible caudal fin. Wi...

Macrophages are essential for appendage regeneration after amputation in regenerative species. The molecular mechanisms through which macrophages orchestrate blastema formation and regeneration are still unclear. Here, we use the genetically tractable and transparent zebrafish larvae to study the functions of polarized macrophage subsets during caudal fin regeneration. After caudal fin amputati...

The symmetrical, flexible teleost fish 'tail' has been a prime example of recapitulation - evolutionary change (phylogeny) mirrored in development (ontogeny). Paleozoic ray-finned fishes (Actinopterygii), relatives of teleosts, exhibited ancestral scale-covered tails curved over their caudal fins. For over 150 years, this arrangement was thought to be retained in teleost larva and overgrown, mi...