Dorsal fin in the context of "Elasmobranch"

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👉 Dorsal fin in the context of Elasmobranch

Elasmobranchii (/ɪˌlæzməˈbræŋki/) is a subclass of Chondrichthyes or cartilaginous fish, including modern sharks (division Selachii), and batomorphs (division Batomorphi, including rays, skates, and sawfish). Members of this subclass are characterised by having five to seven pairs of gill slits opening individually to the exterior, rigid dorsal fins and small placoid scales on the skin. The teeth are in several series; the upper jaw is not fused to the cranium, and the lower jaw is articulated with the upper. The details of this jaw anatomy vary between species, and help distinguish the different elasmobranch clades. The pelvic fins in males are modified to create claspers for the transfer of sperm. There is no swim bladder; instead, these fish maintain buoyancy with large livers rich in oil.

The definition of the clade is unclear with respect to fossil chondrichthyans. Some authors consider it as equivalent to Neoselachii (the crown group clade including modern sharks, rays, and all other descendants of their last common ancestor). Other authors use the name Elasmobranchii for a broader branch-based group of all chondrichthyans more closely related to modern sharks and rays than to Holocephali (the clade containing chimaeras and their extinct relatives). Important extinct groups of elasmobranchs sensu lato include the hybodonts (Order Hybodontiformes), xenacanths (order Xenacanthformes) and Ctenacanthiformes. These are also often referred to as "sharks" in reference to their similar anatomy and ecology to modern sharks.

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Dorsal fin in the context of Secondarily aquatic tetrapods

Several groups of tetrapods have undergone secondary aquatic adaptation, an evolutionary transition from being purely terrestrial to living at least partly aquatic. These animals are called "secondarily aquatic" because although all tetrapods descended from freshwater lobe finned fish (see evolution of tetrapods), their more recent ancestors are terrestrial vertebrates that evolved on land for hundreds of millions of years, and their clades only re-adapted to aquatic environment much later.

Unlike primarily aquatic vertebrates (i.e. fish), secondarily aquatic tetrapods (especially aquatic amniotes), while having appendages such as flippers, dorsal fin and tail fins (flukes) that resemble fish fins due to convergent evolution, still have physiology based on their terrestrial ancestry, most notably their air-breathing respiration via lungs (instead of aquatic respiration via gills) and excretion of nitrogenous waste as urea or uric acid (instead of ammonia like most fish). Nearly all extant aquatic tetrapods are secondarily aquatic, with only larval amphibians (tadpoles) being primarily aquatic with gills, and only some species of paedomorphic mole salamanders (most notably the fully aquatic axolotl) retain the gill-based physiology into adulthood.

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Dorsal fin in the context of Fish fin

Fins are moving appendages protruding from the body of fish that interact with water to generate thrust and lift, which help the fish swim. Apart from the tail or caudal fin, fish fins have no direct articulations with the axial skeleton and are attached to the core only via muscles and ligaments.

Fish fins are distinctive anatomical features with varying internal structures among different clades: in ray-finned fish (Actinopterygii), fins are mainly composed of spreading bony spines or "rays" covered by a thin stretch of scaleless skin, resembling a folding fan; in lobe-finned fish (Sarcopterygii) such as coelacanths and lungfish, fins are short rays based around a muscular central bud internally supported by a jointed appendicular skeleton; in cartilaginous fish (Chondrichthyes) and jawless fish (Agnatha), fins are fleshy "flippers" supported by a cartilaginous skeleton. The limbs of tetrapods, a mostly terrestrial clade evolved from freshwater lobe-finned fish, are homologous to the pectoral and pelvic fins of all jawed fish.

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Dorsal fin in the context of Fin

A fin is a thin appendage or component attached to a larger body or structure. Fins typically function as foils that produce lift or thrust, or provide the ability to steer or stabilize motion while traveling in water, air, or other fluids. Fins are also used to increase surface areas for heat transfer purposes, or simply as ornamentation.

Fins first evolved on fish as a means of locomotion. Fish fins are used to generate thrust and control the subsequent motion. Fish and other aquatic animals, such as cetaceans, actively propel and steer themselves with pectoral and tail fins. As they swim, they use other fins, such as dorsal and anal fins, to achieve stability and refine their maneuvering.

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Dorsal fin in the context of Narwhal

The narwhal (Monodon monoceros) is a species of toothed whale native to the Arctic. It is the only member of the genus Monodon and one of two living representatives of the family Monodontidae. The narwhal is a stocky cetacean with a relatively blunt snout, a large melon, and a shallow ridge in place of a dorsal fin. Males of this species have a large (1.5–3.0 m (4 ft 11 in – 9 ft 10 in)) long tusk, which is a protruding left canine thought to function as a weapon, a tool for feeding, in attracting mates or sensing water salinity. Specially adapted slow-twitch muscles, along with the jointed neck vertebrae and shallow dorsal ridge allow for easy movement through the Arctic environment, where the narwhal spends extended periods at great depths. The narwhal's geographic range overlaps with that of the similarly built and closely related beluga whale, and the animals are known to interbreed.

Narwhals inhabit the Arctic waters of Canada, Greenland and Russia. Every year, they migrate to ice-free summering grounds, usually in shallow waters, and often return to the same sites in subsequent years. Their diet mainly consists of polar and Arctic cod, Greenland halibut, cuttlefish, shrimp, and armhook squid. Diving to depths of up to 2,370 m (7,780 ft), the narwhal is among the deepest-diving cetaceans. The animals typically travel in groups of three to eight, with aggregations of up to 1,000 occurring in the summer months. Narwhals mate among the offshore pack ice from March to May, and the young are born between July and August of the following year. When communicating amongst themselves, narwhals use a variety of clicks, whistles and knocks.

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Dorsal fin in the context of Kogiidae

Kogiidae is a family comprising at least two extant species of Cetacea, the pygmy (Kogia breviceps) and dwarf (K. sima) sperm whales. As their common names suggest, they somewhat resemble sperm whales, with squared heads and small lower jaws, but are much smaller, with much shorter skulls and more notable dorsal fins than sperm whales. Kogiids are also characterized by a "false gill slit" behind their eyes.

A number of extinct genera have been named.

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Dorsal fin in the context of Dwarf sperm whale

The dwarf sperm whale (Kogia sima) is a sperm whale that inhabits temperate and tropical oceans worldwide, in particular continental shelves and slopes. It was first described by biologist Richard Owen in 1866, based on illustrations by naturalist Sir Walter Elliot. The species was considered to be synonymous with the pygmy sperm whale (Kogia breviceps) from 1878 until 1998. The dwarf sperm whale is a small whale, 2 to 2.7 m (6 ft 7 in to 8 ft 10 in) and 136 to 272 kg (300 to 600 lb), that has a grey coloration, square head, small jaw, and robust body. Its appearance is very similar to the pygmy sperm whale, distinguished mainly by the position of the dorsal fin on the body–nearer the middle in the dwarf sperm whale and nearer the tail in the other.

The dwarf sperm whale is a suction feeder that mainly eats squid, and does this in small pods of typically one to four members. It is preyed upon by the killer whale (Orcinus orca) and large sharks such as the great white shark (Carcharodon carcharius). When startled, the whale can eject a cloud of red-brown fluid. Most of what is known of the whale comes from beached individuals, as sightings in the ocean are rare. Many of these stranded whales died from parasitic infestations or heart failure.

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Dorsal fin in the context of Beluga whale

The beluga whale (/bəˈlɡə, bɪ-, bɛˈlʊɡə/; Delphinapterus leucas) is an Arctic and sub-Arctic cetacean. It is one of two living members of the family Monodontidae, along with the narwhal, and the only member of the genus Delphinapterus. It is also known as the white whale, as it is the only cetacean to regularly occur with this colour; the sea canary, due to its high-pitched calls; and the melonhead, though that more commonly refers to the melon-headed whale, which is an oceanic dolphin.

The beluga is adapted to life in the Arctic, with anatomical and physiological characteristics that differentiate it from other cetaceans. Amongst these are its all-white colour and the absence of a dorsal fin, which allows it to swim under ice with ease. It possesses a distinctive protuberance at the front of its head which houses an echolocation organ called the melon, which in this species is large and deformable. The beluga's body size is between that of a dolphin and a true whale, with males growing up to 5.5 m (18 ft) long and weighing up to 1,600 kg (3,530 lb). This whale has a stocky body. Like many cetaceans, a large percentage of its weight is blubber (subcutaneous fat). Its sense of hearing is highly developed and its echolocation allows it to move about and find breathing holes under sheet ice.

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