Actinopterygii
Actinopterygii, members of which are known as ray-finned fish or actinopterygians, is a class of bony fish that constitutes nearly 99% of the over 30,000 living species of fish. The vast majority of extant actinopterygian species are teleosts, and by species count they dominate the subphylum Vertebrata, comprising over 50% of all living vertebrates. They are the most abundant nektonic aquatic animals and are ubiquitous throughout freshwater, brackish and marine environments from the deep sea to subterranean waters to the highest mountain streams. Extant species can range in size from Paedocypris, at, to the giant sunfish, at, and the giant oarfish, at . The largest ever known ray-finned fish, the extinct Leedsichthys from the Jurassic, is estimated to have grown to.
Ray-finned fish 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 fins of the sister clade Sarcopterygii. Resembling folding fans, the actinopterygian fins can easily change shape, orientation 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.
Characteristics
Ray-finned fishes occur in many variant forms. The main features of typical ray-finned fish are shown in the adjacent diagram.The swim bladder is a more derived structure and used for buoyancy. Except from the bichirs, which just like the lungs of lobe-finned fish have retained the ancestral condition of ventral budding from the foregut, the swim bladder in ray-finned fishes derives from a dorsal bud above the foregut. In early forms the swim bladder could still be used for breathing, a trait still present in Holostei. In some fish like the arapaima, the swim bladder has been modified for breathing air again, and in other lineages it has been completely lost.
The teleosts have urinary and reproductive tracts that are fully separated, while the Chondrostei have common urogenital ducts, and partially connected ducts are found in Cladistia and Holostei.
Ray-finned fishes have many different types of scales; but all teleosts have leptoid scales. The outer part of these scales fan out with bony ridges, while the inner part is crossed with fibrous connective tissue. Leptoid scales are thinner and more transparent than other types of scales, and lack the hardened enamel- or dentine-like layers found in the scales of many other fish. Unlike ganoid scales, which are found in non-teleost actinopterygians, new scales are added in concentric layers as the fish grows.
Teleosts and chondrosteans also differ from the bichirs and holosteans in having gone through a whole-genome duplication. The WGD is estimated to have happened about 320 million years ago in the teleosts, which on average has retained about 17% of the gene duplicates, and around 180 million years ago in the chondrosteans. It has since happened again in some teleost lineages, like Salmonidae and several times independently within the Cyprinidae.
Body shapes and fin arrangements
Ray-finned fish vary in size and shape, in their feeding specializations, and in the number and arrangement of their ray-fins.Reproduction
In nearly all ray-finned fish, the sexes are separate, and in most species the females spawn eggs that are fertilized externally, typically with the male inseminating the eggs after they are laid. Development then proceeds with a free-swimming larval stage. However other patterns of ontogeny exist, with one of the commonest being sequential hermaphroditism. In most cases this involves protogyny, fish starting life as females and converting to males at some stage, triggered by some internal or external factor. Protandry, where a fish converts from male to female, is much less common than protogyny.Most families use external rather than internal fertilization. Of the oviparous teleosts, most do not provide parental care. Viviparity, ovoviviparity, or some form of parental care for eggs, whether by the male, the female, or both parents is seen in a significant fraction of the 422 teleost families; no care is likely the ancestral condition. The oldest case of viviparity in ray-finned fish is found in Middle Triassic species of Saurichthys. Viviparity is relatively rare and is found in about 6% of living teleost species; male care is far more common than female care. Male territoriality "preadapts" a species for evolving male parental care.
There are a few examples of fish that self-fertilise. The mangrove rivulus is an amphibious, simultaneous hermaphrodite, producing both eggs and spawn and having internal fertilisation. This mode of reproduction may be related to the fish's habit of spending long periods out of water in the mangrove forests it inhabits. Males are occasionally produced at temperatures below and can fertilise eggs that are then spawned by the female. This maintains genetic variability in a species that is otherwise highly inbred.
Classification and fossil record
Actinopterygii is divided into the subclasses Cladistia, Chondrostei and Neopterygii. The Neopterygii, in turn, is divided into the infraclasses Holostei and Teleostei. During the Mesozoic and Cenozoic the teleosts in particular diversified widely. As a result, 96% of living fish species are teleosts, while all other groups of actinopterygians represent depauperate lineages.The classification of ray-finned fishes can be summarized as follows:
- Cladistia, which include bichirs and reedfish
- Actinopteri, which include:
- * Chondrostei, which include Acipenseriformes
- * Neopterygii, which include:
- **Teleostei
- **Holostei, which include:
- ***Lepisosteiformes
- ***Amiiformes
The polypterids are the sister lineage of all other actinopterygians, the Acipenseriformes are the sister lineage of Neopterygii, and Holostei are the sister lineage of teleosts. The Elopomorpha appear to be the most basal teleosts.
The earliest known fossil actinopterygian is Andreolepis hedei, dating back 420 million years, remains of which have been found in Russia, Sweden, and Estonia. Crown group actinopterygians most likely originated near the Devonian-Carboniferous boundary. The earliest fossil relatives of modern teleosts are from the Triassic period, although it is suspected that teleosts originated already during the Paleozoic Era.
| Chondrostei | Atlantic sturgeon | Chondrostei ' is a subclass of primarily cartilaginous fish showing some ossification. Earlier definitions of Chondrostei are now known to be paraphyletic, meaning that this subclass does not contain all the descendants of their common ancestor. There used to be 52 species divided among two orders, the Acipenseriformes and the Polypteriformes. Reedfish and birchirs are now separated from the Chondrostei into their own sister lineage, the Cladistia. It is thought that the chondrosteans evolved from bony fish but lost the bony hardening of their cartilaginous skeletons, resulting in a lightening of the frame. Elderly chondrosteans show beginnings of ossification of the skeleton, suggesting that this process is delayed rather than lost in these fish. This group had once been classified with the sharks: the similarities are obvious, as not only do the chondrosteans mostly lack bone, but the structure of the jaw is more akin to that of sharks than other bony fish, and both lack scales. Additional shared features include spiracles and, in sturgeons, a heterocercal tail. However the fossil record suggests that these fish have more in common with the Teleostei than their external appearance might suggest. |
| Neopterygii | Atlantic salmon | Neopterygii ' is a subclass of ray-finned fish that appeared somewhere in the Late Permian. There were only few changes during its evolution from the earlier actinopterygians. Neopterygians are a very successful group of fishes because they can move more rapidly than their ancestors. Their scales and skeletons began to lighten during their evolution, and their jaws became more powerful and efficient. While electroreception and the ampullae of Lorenzini is present in all other groups of fish, with the exception of hagfish, neopterygians have lost this sense, though it later re-evolved within Gymnotiformes and catfishes, who possess nonhomologous teleost ampullae. |
File:Cheirolepis canadensis.jpg|thumb|Fossil of the Devonian cheirolepidiform Cheirolepis canadensis
File:Elonichthys peltigerus.jpg|thumb|Fossil of the Carboniferous elonichthyiform Elonichthys peltigerus
File:Aeduella sp.JPG|thumb|Fossil of the Permian aeduelliform Aeduella blainvillei
File:PalaeoniscusFreieslebenensis-NaturalHistoryMuseum-August23-08.jpg|thumb|Fossil of the Permian palaeonisciform Palaeoniscum freieslebeni
File:Bobasatrania canadensis 1.jpg|thumb|Fossil of the Triassic bobasatraniiform Bobasatrania canadensis
File:Italopterus magnificus 01.jpg|thumb|Fossil of the Triassic perleidiform Thoracopterus magnificus
File:Prohalecites sp Rasa 1.JPG|thumb|Fossils of the Triassic prohaleciteiform Prohalecites sp., the earliest teleosteomorph
File:Aspidorhynchus sp.jpg|thumb|Fossil of the Jurassic aspidorhynchiform Aspidorhynchus sp.
File:Pachycormus curtus SMNS 55300.jpg|thumb|Fossil of the Jurassic pachycormiform Pachycormus curtus
File:Yanosteus longidorsalis MHNT.jpg|thumb|Fossil of the Cretaceous acipenseriform Yanosteus longidorsalis
File:Nematonotus longispinus.jpg|thumb|Fossil of the Cretaceous aulopiform Nematonotus longispinus
File:Thrissops formosus 3.JPG|thumb|Fossil of the Cretaceous ichthyodectiform Thrissops formosus
File:Mene oblonga 23.JPG|thumb|Fossil of the Eocene carangiform Mene oblonga
File:Amphistium.JPG|thumb|Fossil of the Eocene pleuronectiform Amphistium paradoxum
File:Priscacara serrata FMNH PF13014 img1.jpg|thumb|right|Fossil of a ray-finned perch from the Lower Eocene about 50 million years ago
File:Nerophis.jpg|thumb|Fossil of the Miocene syngnathiform ''Nerophis zapfei''