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Chondrichthyes

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Cartilaginous fishes
Temporal range: 439–0 Ma Early Silurian (Aeronian) - Present
Example of cartilaginous fishes: Elasmobranchii at the top of the image and Holocephali at the bottom of the image.
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Clade: Eugnathostomata
Class: Chondrichthyes
Huxley, 1880
Living subclasses and orders

Chondrichthyes (/kɒnˈdrɪkθiz/; from Ancient Greek χόνδρος (khóndros) 'cartilage' and ἰχθύς (ikhthús) 'fish') is a class of jawed fish that contains the cartilaginous fish or chondrichthyans, which all have skeletons 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 vertebrates with paired fins, paired nares, placoid scales, conus arteriosus in the heart, and a lack of opercula and swim bladders. Within the infraphylum Gnathostomata, cartilaginous fishes are distinct from all other jawed vertebrates.

The class is divided into two subclasses: Elasmobranchii (sharks, rays, skates and sawfish) and Holocephali (chimaeras, sometimes called ghost sharks, which are sometimes separated into their own class). Extant chondrichthyans range in size from the 10 cm (3.9 in) finless sleeper ray to the over 10 m (33 ft) whale shark.

Anatomy

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Skeleton

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The skeleton is cartilaginous. The notochord is gradually replaced by a vertebral column during development, except in Holocephali, where the notochord stays intact. In some deepwater sharks, the column is reduced.[9]

As they do not have bone marrow, red blood cells are produced in the spleen and the epigonal organ (special tissue around the gonads, 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.

Appendages

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Apart from electric rays, which have a thick and flabby body, with soft, loose skin, chondrichthyans have tough skin covered with dermal teeth (again, Holocephali is an exception, as the teeth are lost in adults, only kept on the clasping organ seen on the caudal ventral surface of the male), also called placoid scales (or dermal denticles), making it feel like sandpaper. In most species, all dermal denticles are oriented in one direction, making the skin feel very smooth if rubbed in one direction and very rough if rubbed in the other.

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 rays, 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.[10]

Body covering

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Chondrichthyans have tooth-like scales called dermal denticles or placoid scales. Denticles usually provide protection, and in most cases, streamlining. Mucous glands exist in some species, as well.

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 teleost 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[by whom?] 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.

Respiratory system

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All chondrichthyans breathe through five to seven pairs of gills, depending on the species. In general, pelagic species must keep swimming to keep oxygenated water moving through their gills, whilst demersal species can actively pump water in through their spiracles and out through their gills. However, this is only a general rule and many species differ.

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.

Nervous system

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Regions of a Chondrichthyes brain colored and labeled on dissected skate. The rostral end of the skate is to the right.

In chondrichthyans, the nervous system is composed of a small brain, 8–10 pairs of cranial nerves, and a spinal cord with spinal nerves.[11] They have several sensory organs which provide information to be processed. Ampullae of Lorenzini are a network of small jelly filled pores called electroreceptors which help the fish sense electric fields in water. This aids in finding prey, navigation, and sensing temperature. The Lateral line system has modified epithelial cells located externally which sense motion, vibration, and pressure in the water around them. Most species have large well-developed eyes. Also, they have very powerful nostrils and olfactory organs. Their inner ears consist of 3 large semicircular canals which aid in balance and orientation. Their sound detecting apparatus has limited range and is typically more powerful at lower frequencies. Some species have electric organs which can be used for defense and predation. They have relatively simple brains with the forebrain not greatly enlarged. The structure and formation of myelin in their nervous systems are nearly identical to that of tetrapods, which has led evolutionary biologists to believe that Chondrichthyes were a cornerstone group in the evolutionary timeline of myelin development.[12]

Immune system

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Like all other jawed vertebrates, members of Chondrichthyes have an adaptive immune system.[13]

Reproduction

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Fertilization is internal. Development is usually live birth (ovoviviparous species) but can be through eggs (oviparous). Some rare species are viviparous. There is no parental care after birth; however, some chondrichthyans do guard their eggs.

Capture-induced premature birth and abortion (collectively called capture-induced parturition) occurs frequently in sharks/rays when fished.[14] 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).[14]

Classification

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The class Chondrichthyes has two subclasses: the subclass Elasmobranchii (sharks, rays, skates, and sawfish) and the subclass Holocephali (chimaeras). To see the full list of the species, click here.

Subclasses of cartilaginous fishes
Elasmobranchii
Elasmobranchii is a subclass that includes the sharks and the rays and skates. Members of the elasmobranchii have no swim bladders, five to seven pairs of gill clefts opening individually to the exterior, rigid dorsal fins, and small placoid scales. 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 eyes have a tapetum lucidum. The inner margin of each pelvic fin in the male fish is grooved to constitute a clasper for the transmission of sperm. These fish are widely distributed in tropical and temperate waters.[15]
Holocephali Holocephali (complete-heads) is a subclass of which the order Chimaeriformes is the only surviving group. This group includes the rat fishes (e.g., Chimaera), rabbit-fishes (e.g., Hydrolagus) and elephant-fishes (Callorhynchus). Today, they preserve some features of elasmobranch life in Paleaozoic times, though in other respects they are aberrant. They live close to the bottom and feed on molluscs and other invertebrates. The tail is long and thin and they move by sweeping movements of the large pectoral fins. There is an erectile spine in front of the dorsal fin, sometimes poisonous. There is no stomach (that is, the gut is simplified and the 'stomach' is merged with the intestine), and the mouth is a small aperture surrounded by lips, giving the head a parrot-like appearance.

The fossil record of the Holocephali starts in the Devonian period. The record is extensive, but most fossils are teeth, and the body forms of numerous species are not known, or at best poorly understood.

Extant orders of cartilaginous fishes
Group Order Image Common name Authority Families Genera Species Note
Total
Galean
sharks
Carcharhiniformes ground
sharks
Compagno, 1977 8 51 >270 7 10 21
Heterodontiformes bullhead
sharks
L. S. Berg, 1940 1 1 9
Lamniformes mackerel
sharks
L. S. Berg, 1958 7
+2 extinct
10 16 10
Orectolobiformes carpet
sharks
Applegate, 1972 7 13 43 7
Squalomorph
sharks
Hexanchiformes frilled
and
cow sharks
de Buen, 1926 2
+3 extinct
4
+11 extinct
7
+33 extinct
Pristiophoriformes sawsharks L. S. Berg, 1958 1 2 6
Squaliformes dogfish
sharks
Goodrich, 1909 7 23 126 1 6
Squatiniformes angel
sharks
Buen, 1926 1 1 24 3 4 5
Rays Myliobatiformes stingrays
and
relatives
Compagno, 1973 10 29 223 1 16 33
Rhinopristiformes sawfishes 1 2 5–7 5–7
Rajiformes skates
and
guitarfishes
L. S. Berg, 1940 5 36 >270 4 12 26
Torpediniformes electric
rays
de Buen, 1926 2 12 69 2 9
Holocephali Chimaeriformes chimaera Obruchev, 1953 3
+2 extinct
6
+3 extinct
39
+17 extinct

Evolution

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Cartilaginous fish are considered to have evolved from acanthodians. The discovery of Entelognathus and several examinations of acanthodian characteristics indicate that bony fish evolved directly from placoderm like ancestors, while acanthodians represent a paraphyletic assemblage leading to Chondrichthyes. Some characteristics previously thought to be exclusive to acanthodians are also present in basal cartilaginous fish.[18] In particular, new phylogenetic studies find cartilaginous fish to be well nested among acanthodians, with Doliodus and Tamiobatis being the closest relatives to Chondrichthyes.[19] Recent studies vindicate this, as Doliodus had a mosaic of chondrichthyan and acanthodian traits.[20] Dating back to the Middle and Late Ordovician Period, many isolated scales, made of dentine and bone, have a structure and growth form that is chondrichthyan-like. They may be the remains of stem-chondrichthyans, but their classification remains uncertain.[21][22][23]

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.[24][25] Shenacanthus vermiformis, which lived 436 million years ago, had thoracic armour plates resembling those of placoderms.[26]

By the start of the Early Devonian, 419 million years ago, jawed fishes had divided into three distinct groups: the now extinct placoderms (a paraphyletic assemblage of ancient armoured fishes), the bony fishes, 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.

Extinct orders of cartilaginous fishes
Group Order Image Common name Authority Families Genera Species Note
Holocephali †Orodontiformes
†Petalodontiformes Petalodonts Zangerl, 1981 4 Members of the holocephali, some genera resembled parrot fish, but some members of the Janassidae resembled skates.
†Helodontiformes
†Iniopterygiformes Members of the holocephali that resembled flying fish, are often characterized by large eyes, large upturned pectoral fins, and club-like tails.
†Debeeriiformes
†Symmoriida Symmoriids Zangerl, 1981 (sensu Maisey, 2007) 4 Members of the holocephali, they were heavily sexually dimorphic.[27]
†Eugeneodontida Eugeneodonts Eugeneodontida

Zangerl, 1981

4 Members of the holocephali, they are characterized by large tooth whorls in their jaws.[28]
†Psammodonti-
formes
Position uncertain
†Copodontiformes
†Squalorajiformes
†Chondrenchelyi-
formes
†Menaspiformes
†Cochliodontiformes
Squalomorph
sharks
†Protospinaci-
formes
Other †Squatinactiformes Cappetta et al., 1993 1 1
†Protacrodonti-
formes
†Cladoselachi-
formes
Dean, 1894 1 2 Holocephalans, and potential members of the symmoriida.
†Xenacanthiformes Xenacanths Glikman, 1964 4 Eel-like elasmobranchs that were some of the top freshwater predators of the late Paleozoic.
†Ctenacanthi-
formes
Ctenacanths Glikman, 1964 2 Shark-like elasmobranchs characterized by their robust heads and large dorsal fin spines.
†Hybodontiformes Hybodonts Patterson, 1966 5 Shark-like elasmobranchs distinguished by their conical tooth shape, and the presence of a spine on each of their two dorsal fins.

Taxonomy

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Subphylum Vertebrata
└─Infraphylum Gnathostomata
      ├─Placodermiextinct (armored gnathostomes)
      └Eugnathostomata (true jawed vertebrates)
         ├─Acanthodii (stem cartilaginous fish)
         └─Chondrichthyes (true cartilaginous fish)
             ├─Holocephali (chimaeras + several extinct clades)
             └Elasmobranchii (shark and rays)
                ├─Selachii (true sharks)
                └─Batoidea (rays and relatives)

 

  • Note: Lines show evolutionary relationships.

See also

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References

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  20. ^ Maisey, John G.; Miller, Randall; Pradel, Alan; Denton, John S.S.; Bronson, Allison; Janvier, Philippe (2017). "Pectoral Morphology in Doliodus: Bridging the 'Acanthodian'-Chondrichthyan Divide" (PDF). American Museum Novitates (3875): 1–15. doi:10.1206/3875.1. S2CID 44127090. Archived (PDF) from the original on 9 October 2022.
  21. ^ Andreev, Plamen S.; Coates, Michael I.; Shelton, Richard M.; Cooper, Paul R.; Smith, M. Paul; Sansom, Ivan J. (2015). "Ordovician chondrichthyan-like scales from North America". Palaeontology. 58 (4): 691–704. doi:10.1111/pala.12167. S2CID 140675923.
  22. ^ Sansom, Ivan J.; Davies, Neil S.; Coates, Michael I.; Nicoll, Robert S.; Ritchie, Alex (2012). "Chondrichthyan-like scales from the Middle Ordovician of Australia". Palaeontology. 55 (2): 243–247. Bibcode:2012Palgy..55..243S. doi:10.1111/j.1475-4983.2012.01127.x.
  23. ^ Andreev, Plamen; Coates, Michael I.; Karatajūtė-Talimaa, Valentina; Shelton, Richard M.; Cooper, Paul R.; Wang, Nian-Zhong; Sansom, Ivan J. (2016). "The systematics of the Mongolepidida (Chondrichthyes) and the Ordovician origins of the clade". PeerJ. 4: e1850. doi:10.7717/peerj.1850. PMC 4918221. PMID 27350896.
  24. ^ Andreev, Plamen S.; Sansom, Ivan J.; Li, Qiang; Zhao, Wenjin; Wang, Jianhua; Wang, Chun-Chieh; Peng, Lijian; Jia, Liantao; Qiao, Tuo; Zhu, Min (September 2022). "Spiny chondrichthyan from the lower Silurian of South China". Nature. 609 (7929): 969–974. Bibcode:2022Natur.609..969A. doi:10.1038/s41586-022-05233-8. PMID 36171377. S2CID 252570103.
  25. ^ Andreev, Plamen S.; Sansom, Ivan J.; Li, Qiang; Zhao, Wenjin; Wang, Jianhua; Wang, Chun-Chieh; Peng, Lijian; Jia, Liantao; Qiao, Tuo; Zhu, Min (28 September 2022). "The oldest gnathostome teeth". Nature. 609 (7929): 964–968. Bibcode:2022Natur.609..964A. doi:10.1038/s41586-022-05166-2. ISSN 0028-0836. PMID 36171375. S2CID 252569771.
  26. ^ Zhu, Y. A.; Li, Q.; Lu, J.; Chen, Y.; Wang, J.; Gai, Z.; Zhao, W.; Wei, G.; Yu, Y.; Ahlberg, P. E.; Zhu, M. (2022). "The oldest complete jawed vertebrates from the early Silurian of China". Nature. 609 (7929): 954–958. Bibcode:2022Natur.609..954Z. doi:10.1038/s41586-022-05136-8. PMID 36171378. S2CID 252569910.
  27. ^ Coates, M.; Gess, R.; Finarelli, J.; Criswell, K.; Tietjen, K. (2016). "A symmoriiform chondrichthyan braincase and the origin of chimaeroid fishes". Nature. 541 (7636): 208–211. Bibcode:2017Natur.541..208C. doi:10.1038/nature20806. PMID 28052054. S2CID 4455946.
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Further reading

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