Pelvic fins or ventral fins are paired fins located on the ventral (belly) surface of fish, and are the lower of the only two sets of paired fins (the other being the laterally positioned pectoral fins). The pelvic fins are homologous to the hindlimbs of tetrapods, [1] which evolved from lobe-finned fish during the Middle Devonian.
In actinopterygians, the pelvic fin consists of two endochondrally-derived bony girdles attached to bony radials. Dermal fin rays (lepidotrichia) are positioned distally from the radials. There are three pairs of muscles each on the dorsal and ventral side of the pelvic fin girdle that abduct and adduct the fin from the body.[ citation needed ]
Pelvic fin structures can be extremely specialized in actinopterygians. Gobiids and lumpsuckers modify their pelvic fins into a sucker disk that allow them to adhere to the substrate or climb structures, such as waterfalls. [2] In priapiumfish, males have modified their pelvic structures into a spiny copulatory device that grasps the female during mating. [3]
In actinopterygian steady state swimming, the pelvic fins are actively controlled and used to provide powered corrective forces. [4] [5] Careful timing of the pelvic fin movement during whole-body movements allows the pelvic fins to generate forces that dampen the forces from the entire body, therefore stabilizing the fish. For maneuvers, electromyogram data shows that pelvic fin muscles are activated after the start of the maneuver, indicating that the fins are used more for stabilization instead of generating the maneuver. [4]
In rays and skates, pelvic fins can be used for "punting," where they asynchronously or synchronously push off the substrate to propel the animal forwards. [6]
Unlike limb development in tetrapods, where the forelimb and hindlimb buds emerge at roughly the same timepoint, the pelvic fin bud emerges much later than the pectoral fin. [7] While the pectoral fin bud is apparent at 36 hours post fertilization (hpf) in zebrafish, the pelvic fin bud is only clear at around 21 days post fertilization (dpf), roughly when the animal is 8 mm in length.[ citation needed ]
In zebrafish, the pelvic fin bud starts as a mesenchymal condensation that forms an apical ectodermal thickening. [7] A fin fold forms from this thickening, which is then invaded by migratory mesenchyme, separating the fin bud into the proximal mesenchyme (which will give rise to the endoskeletal girdle and radials) and the distal mesenchyme (which will give rise to dermal fin rays). [7]
Actinopterygii, members of which are known as ray-finned fish or actinopterygians, is a class of bony fish that comprise over 50% of living vertebrate species. They are so called because of their lightly built fins made of webbings of skin supported by radially extended thin bony spines called lepidotrichia, as opposed to the bulkier, fleshy lobed fins of the sister class Sarcopterygii. Resembling folding fans, the actinopterygian fins can easily change shape and wetted area, providing superior thrust-to-weight ratios per movement compared to sarcopterygian and chondrichthyian fins. The fin rays attach directly to the proximal or basal skeletal elements, the radials, which represent the articulation between these fins and the internal skeleton.
The zebrafish is a freshwater fish belonging to the minnow family (Cyprinidae) of the order Cypriniformes. Native to India and South Asia, it is a popular aquarium fish, frequently sold under the trade name zebra danio. It is also found in private ponds.
Gobiidae or gobies is a family of bony fish in the order Gobiiformes, one of the largest fish families comprising more than 2,000 species in more than 200 genera. Most of gobiid fish are relatively small, typically less than 10 cm (3.9 in) in length, and the family includes some of the smallest vertebrates in the world, such as Trimmatom nanus and Pandaka pygmaea, Trimmatom nanus are under 1 cm long when fully grown, then Pandaka pygmaea standard length are 9 mm (0.35 in), maximum known standard length are 11 mm (0.43 in). Some large gobies can reach over 30 cm (0.98 ft) in length, but that is exceptional. Generally, they are benthic or bottom-dwellers. Although few are important as food fish for humans, they are of great significance as prey species for other commercially important fish such as cod, haddock, sea bass and flatfish. Several gobiids are also of interest as aquarium fish, such as the dartfish of the genus Ptereleotris. Phylogenetic relationships of gobiids have been studied using molecular data.
Gasterosteoidei is a suborder of ray-finned fishes that includes the sticklebacks and relatives, the 5th edition of Fishes of the World classifies this suborder within the order Scorpaeniformes.
The Cyclopteridae are a family of marine fishes, commonly known as lumpsuckers or lumpfish, in the order Scorpaeniformes. They are found in the cold waters of the Arctic, North Atlantic, and North Pacific oceans. The greatest number of species are found in the North Pacific. The family name Cyclopteridae derives from the Greek words κύκλος (kyklos), meaning "circle", and πτέρυξ (pteryx), meaning "wing" or "fin", in reference to the circle-shaped pectoral fins of most of the fish in this family.
Panderichthys is a genus of extinct sarcopterygian from the late Devonian period, about 380 Mya. Panderichthys, which was recovered from Frasnian deposits in Latvia, is represented by two species. P. stolbovi is known only from some snout fragments and an incomplete lower jaw. P. rhombolepis is known from several more complete specimens. Although it probably belongs to a sister group of the earliest tetrapods, Panderichthys exhibits a range of features transitional between tristichopterid lobe-fin fishes and early tetrapods. It is named after the German-Baltic paleontologist Christian Heinrich Pander. Possible tetrapod tracks dating back to before the appearance of Panderichthys in the fossil record were reported in 2010, which suggests that Panderichthys is not a direct ancestor of tetrapods, but nonetheless shows the traits that evolved during the fish-tetrapod evolution
Stethacanthus is an extinct genus of shark-like holocephalians which lived from the Late Devonian to Late Carboniferous epoch, dying out around 298.9 million years ago. Fossils have been found in Australia, Asia, Europe and North America.
Tiktaalik is a monospecific genus of extinct sarcopterygian from the Late Devonian Period, about 375 Mya, having many features akin to those of tetrapods. Tiktaalik is estimated to have had a total length of 1.25–2.75 metres (4.1–9.0 ft) based on various specimens.
This glossary of ichthyology is a list of definitions of terms and concepts used in ichthyology, the study of fishes.
The apical ectodermal ridge (AER) is a structure that forms from the ectodermal cells at the distal end of each limb bud and acts as a major signaling center to ensure proper development of a limb. After the limb bud induces AER formation, the AER and limb mesenchyme—including the zone of polarizing activity (ZPA)—continue to communicate with each other to direct further limb development.
Kenichthys is a genus of sarcopterygian fish from the Devonian period, and a member of the clade Tetrapodomorpha. The only known species of the genus is Kenichthys campbelli, the first remains of which were found in China in 1993. The genus is important to the study of the evolution of tetrapods due to the unique nature of its nostrils, which provide vital evidence regarding the evolutionary transition of fish-like nostrils to the tetrapod choanae.
A limb is a jointed, muscled appendage of a tetrapod vertebrate animal used for weight-bearing, terrestrial locomotion and physical interaction with other objects. The distalmost portion of a limb is known as its extremity. The limbs' bony endoskeleton, known as the appendicular skeleton, is homologous among all tetrapods, who use their limbs for walking, running and jumping, swimming, climbing, grasping, touching and striking.
Fin and flipper locomotion occurs mostly in aquatic locomotion, and rarely in terrestrial locomotion. From the three common states of matter — gas, liquid and solid, these appendages are adapted for liquids, mostly fresh or saltwater and used in locomotion, steering and balancing of the body. Locomotion is important in order to escape predators, acquire food, find mates and bury for shelter, nest or food. Aquatic locomotion consists of swimming, whereas terrestrial locomotion encompasses walking, 'crutching', jumping, digging as well as covering. Some animals such as sea turtles and mudskippers use these two environments for different purposes, for example using the land for nesting, and the sea to hunt for food.
A sucker in zoology is a specialised attachment organ of an animal. It acts as an adhesion device in parasitic worms, several flatworms, cephalopods, certain fishes, amphibians, and bats. It is a muscular structure for suction on a host or substrate. In parasitic annelids, flatworms and roundworms, suckers are the organs of attachment to the host tissues. In tapeworms and flukes, they are a parasitic adaptation for attachment on the internal tissues of the host, such as intestines and blood vessels. In roundworms and flatworms they serve as attachment between individuals particularly during mating. In annelids, a sucker can be both a functional mouth and a locomotory organ. The structure and number of suckers are often used as basic taxonomic diagnosis between different species, since they are unique in each species. In tapeworms there are two distinct classes of suckers, namely "bothridia" for true suckers, and "bothria" for false suckers. In digeneal flukes there are usually an oral sucker at the mouth and a ventral sucker posterior to the mouth. Roundworms have their sucker just in front of the anus; hence it is often called a pre-anal sucker.
Fins are moving appendages protruding from the body of fish that interact with water to generate thrust and help the fish swim. Apart from the tail or caudal fin, fish fins have no direct connection with the spine and are supported only by muscles.
The smooth lumpfish is a species of marine ray-finned fish belonging to the family Cyclopteridae, the lumpfishes and lumpsuckers. This species is found in the northern Pacific Ocean. It is the only species in the monospecific genus Aptocyclus.
The flathead congoli is a species of marine ray-finned fish, belonging to the family Bovichtidae, the thornfishes or temperate icefishes. It is native to the seas off southeastern Australia. This species is the only known member of its genus.
Microbrachius is an extinct genus of tiny, advanced antiarch placoderms closely related to the bothriolepids. Specimens range in age from the Lower Devonian Late Emsian Stage to the Middle Devonian Upper Givetian Stage. They are characterized by having large heads with short thoracic armor of an average length of 2–4 cm. There are patterns of small, but noticeable tubercles on the armor, with the arrangement varying from species to species. Specimens of Microbrachius have been found in Scotland, Belarus, Estonia, and China.
Innovations conventionally associated with terrestrially first appeared in aquatic elpistostegalians such as Panderichthys rhombolepis, Elpistostege watsoni, and Tiktaalik roseae. Phylogenetic analyses distribute the features that developed along the tetrapod stem and display a stepwise process of character acquisition, rather than abrupt. The complete transition occurred over a period of 30 million years beginning with the tetrapodomorph diversification in the Middle Devonian.
Plesioselachus is an extinct genus of Late Devonian (Famennian) cartilaginous fish with uncertain classification, which contains only one species, P. macracanthus from the Waterloo Farm lagerstätte in South Africa. Known from a single incomplete articulated skeleton and some isolated remains, it is characterized by having a long dorsal spine with length about one third of body length.
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