Chondrichthyes (; ) is a class of jawed fish that contains the cartilaginous fish or chondrichthyans, which all have primarily composed of cartilage. They can be contrasted with the Osteichthyes or bony fish, which have skeletons primarily composed of bone tissue. Chondrichthyes are aquatic animal with paired fins, paired Nostril, , conus arteriosus in the heart, and a lack of opercula and . Within the infraphylum Gnathostomata, cartilaginous fishes are distinct from all other jawed vertebrates.
The class is divided into two subclasses: Elasmobranchii (, Batoidea, skates and sawfish) and Holocephali (, sometimes called ghost sharks, which are sometimes separated into their own class). Extant chondrichthyans range in size from the finless sleeper ray to the over whale shark.
As they do not have bone marrow, red blood cells are produced in the spleen and the epigonal organ (special tissue around the , which is also thought to play a role in the immune system). They are also produced in the Leydig's organ, which is only found in certain cartilaginous fishes. The subclass Holocephali, which is a very specialized group, lacks both the Leydig's and epigonal organs.
Originally, the pectoral and pelvic girdles, which do not contain any dermal elements, did not connect. In later forms, each pair of fins became ventrally connected in the middle when scapulocoracoid and puboischiadic bars evolved. In Batoidea, the pectoral fins are connected to the head and are very flexible.
One of the primary characteristics present in most sharks is the heterocercal tail, which aids in locomotion.
It is assumed that their oral teeth evolved from dermal denticles that migrated into the mouth, but it could be the other way around, as the Teleostei bony fish Denticeps clupeoides has most of its head covered by dermal teeth (as does, probably, Atherion elymus, another bony fish). This is most likely a secondary evolved characteristic, which means there is not necessarily a connection between the teeth and the original dermal scales.
The old placoderms did not have teeth at all, but had sharp bony plates in their mouth. Thus, it is unknown whether the dermal or oral teeth evolved first. It has even been suggested that the original bony plates of all vertebrates are now gone and that the present scales are just modified teeth, even if both the teeth and body armor had a common origin a long time ago. However, there is currently no evidence of this.
A spiracle is a small hole found behind each eye. These can be tiny and circular, such as found on the nurse shark ( Ginglymostoma cirratum), to extended and slit-like, such as found on the wobbegongs (Orectolobidae). Many larger, pelagic species, such as the mackerel sharks (Lamnidae) and the thresher sharks (Alopiidae), no longer possess them.
Capture-induced premature birth and abortion (collectively called capture-induced parturition) occurs frequently in sharks/rays when fished. Capture-induced parturition is often mistaken for natural birth by recreational fishers and is rarely considered in commercial fisheries management despite being shown to occur in at least 12% of live bearing sharks and rays (88 species to date).
| ground sharks | Leonard Compagno, 1977 | 8 | 51 | >270 | 7 | 10 | 21 | ||||
| bullhead sharks | Lev Berg, 1940 | 1 | 1 | 9 | |||||||
| mackerel sharks | Lev Berg, 1958 | 7 +2 extinct | 10 | 16 | 10 | ||||||
| carpet sharks | Applegate, 1972 | 7 | 13 | 43 | 7 | ||||||
| Hexanchiformes | de Buen, 1926 | 2 +3 extinct | 4 +11 extinct | 7 +33 extinct | |||||||
| sawsharks | Lev Berg, 1958 | 1 | 2 | 6 | |||||||
| dogfish sharks | Goodrich, 1909 | 7 | 23 | 126 | 1 | 6 | |||||
| angel sharks | Buen, 1926 | 1 | 1 | 24 | 3 | 4 | 5 | ||||
| Myliobatiformes | Compagno, 1973 | 10 | 29 | 223 | 1 | 16 | 33 | ||||
| sawfishes | 1 | 2 | 5–7 | 5–7 | |||||||
| Rajiformes | Lev Berg, 1940 | 5 | 36 | >270 | 4 | 12 | 26 | ||||
| electric rays | de Buen, 1926 | 2 | 12 | 69 | 2 | 9 | |||||
| chimaera | Dmitry Obruchev, 1953 | 3 +2 extinct | 6 +3 extinct | 39 +17 extinct |
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The earliest unequivocal fossils of acanthodian-grade cartilaginous fishes are Qianodus and Fanjingshania from the early Silurian (Aeronian) of Guizhou, China around 439 million years ago, which are also the oldest unambiguous remains of any jawed vertebrates. Shenacanthus vermiformis, which lived 436 million years ago, had thoracic armour plates resembling those of placoderms.
By the start of the Early Devonian, 419 million years ago, had divided into three distinct groups: the now extinct (a paraphyletic assemblage of ancient armoured fishes), the , and the clade that includes spiny sharks and early cartilaginous fish. The modern bony fishes, class Osteichthyes, appeared in the late Silurian or early Devonian, about 416 million years ago. The first abundant genus of shark, Cladoselache, appeared in the oceans during the Devonian Period. The first cartilaginous fishes evolved from Doliodus-like spiny shark ancestors.
| Orodontiformes | Zangerl, 1981 | 2 | Early members of Chondrichthyes based mostly on teeth. Includes many species that are unrelated to one another. (2026). 9783899371161, F. Pfeil. ISBN 9783899371161 | |||||
| Petalodonts | Patterson, 1965 (equiv. to Petalodontida Zangerl, 1981) | 5 or 6 | Members of holocephali. Some resembled skates or rays, while others were compressed and had beak-like jaws. | |||||
| Helodus | Patterson, 1965 | 1 | 1 | 1? | Members of Holocephali based mostly on teeth. A single species is known from skeletal fossils. | |||
| Iniopterygians | Zangerl & Case, 1973 (as Iniopterygia) | 2 | Early chondrichthyans that resembled flying fish. May be members of Holocephali. | |||||
| Grogan & Lund, 2000 | 1 | 2 | 2 | Members of Holocephali with a primitive form of jaw suspension called autodiastyly. | ||||
| Symmoriidae | Zangerl, 1981 (sensu Maisey, 2007) | 2 or 3 | Potential members of Holocephali that were heavily sexually dimorphic. Males had an organ called a "spine-brush complex" instead of a first dorsal fin. | |||||
| Eugeneodontida | Zangerl, 1981 (as Eugeneodontida) | 4 or 5 | Members of holocephali, they are characterized by large tooth whorls in their jaws. | |||||
| Obruchev, 1953 | 1 | Members of Holocephali, almost exclusively known from teeth. A single skull is known, which had armor plates. | ||||||
| Obruchev, 1953 | 1 | Members of Holocephali. Relationships and appearance are uncertain as this order is only known from teeth. | ||||||
| 1 | 2? | 2? | Members of Holocephali, sometimes included in Chimaeriformes. | |||||
| Patterson, 1965 | 2 | Members of Holocephali with eel-like bodies and teeth similar to modern chimaeras. Members are sexually dimorphic. | ||||||
| Obruchev, 1953 (equiv. to Menaspoidei Patterson, 1965) | 3 | Members of Holocephali with heavy armor plating. Historically misinterpreted as Placoderm or Ostracoderm. | ||||||
| Cochliodonts | Obruchev, 1953 | 2 | Members of Holocephali known almost exclusively from teeth; some body fossils are known but have not been described. | |||||
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| Other | Cappetta et al., 1993 | 1 | 1 | 1 | Early chondrichthyans with ray-like bodies. | |||
| Zangerl, 1981 | 1 | Early members of Elasmobranchii. | ||||||
| Dean, 1894 | 1 | 2 | Potentially members of Holocephali and of the Symmoriiformes. | |||||
| Xenacanthida | Glikman, 1964 | 2 or 3 | Eel-like chondrichthyans that typically lived in freshwater. May be members of Elasmobranchii. | |||||
| Ctenacanths | Glikman, 1964 | 1 or 2 | Shark-like chondrichthyans characterized by their robust heads and large dorsal fin spines. May be members of Elasmobranchii | |||||
| Hybodontiformes | Patterson, 1966 | 10 or 11 | Shark-like elasmobranchs distinguished by their conical tooth shape, and the presence of a spine on each of their two dorsal fins. |
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