The ray-finned fishes are so called because they possess lepidotrichia or "fin rays", their fins being webs of skin supported by bony or horny spines ("rays"), as opposed to the fleshy, lobed fins that characterize the class Sarcopterygii which also, however, possess lepidotrichia. These actinopterygian fin rays attach directly to the proximal or basal skeletal elements, the radials, which represent the link or connection between these fins and the internal skeleton (e.g., pelvic and pectoral girdles).
In terms of numbers, actinopterygians are the dominant class of vertebrates, comprising nearly 99% of the over 30,000 species of fish (Davis, Brian 2010). They are ubiquitous throughout freshwater and marine environments from the deep sea to the highest mountain streams. Extant species can range in size from Paedocypris, at 8 mm (0.3 in), to the massive ocean sunfish, at 2,300 kg (5,070 lb), and the long-bodied oarfish, at 11 m (36 ft).
Traditionally actinopterygians have been divided into the subclasses Chondrostei and Neopterygii. Neopterygii, in turn, have been divided into the infraclasses Holostei and Teleostei. Some morphological evidence suggests the Neopterygii is paraphyletic; however, recent work, based on taxon orders, is arranged in what has been suggested to represent the evolutionary sequence down to the level of order, based primarily on the long history of morphological studies. This classification, like any other taxonomy based on phylogenetic research, has been in a state of flux. Recent morphological and molecular data have shown several of these ordinal and higher-level groupings represent evolutionary grades rather than clades. Examples of demonstrably paraphyletic groups include the Paracanthopterygii, Scorpaeniformes, and Perciformes.
Chondrostei(cartilage bone) are primarily cartilaginous fish showing some ossification. There are 52 species divided among two orders, the Acipenseriformes (sturgeons(pictured) and paddlefishes) and the Polypteriformes (reedfishes and bichirs). It is thought that the ancestors of the chondrosteans were bony fish but that this characteristic was lost in later evolutionary development, resulting in a lightening of the frame. Elderly chondrosteans show beginnings of ossification of the skeleton which suggests that this process is delayed rather than lost in these fish. This group has at times been classified with the sharks: the similarities are obvious, not only do the chondrosteans mostly lack bone, the structure of the jaw is more akin to that of sharks than other bony fish, and both lack scales (excluding the Polypteriforms). Additional shared features include spiracles and, in sturgeons, a heterocercal tail (the vertebrae extend into the larger lobe of the caudal fin). However the fossil record suggests that these fish have more in common with the Teleostei than their external appearance might suggest. Chondrostei is paraphyletic meaning that this subclass does not contain all the descendants of their common ancestor; reclassification of the Chondrostei is therefore not out of the question.
Neopterygii(new fins) appeared somewhere in the Late Permian, before the time of the dinosaurs. There are only few changes during their evolution from the earlier actinopterygians. They 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, Neopterygii has lost this sense, though it later re-evolved within Gymnotiformes and catfishes, who possess nonhomologous teleost ampullae.
Skeleton of the angler fish, Lophius piscatorius. The first spine of the dorsal fin of the anglerfish is modified so it functions like a fishing rod with a lure