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Chondrichthyes (; ) is a class of that contains the cartilaginous fish or chondrichthyans, which all have primarily composed of . They can be contrasted with the or bony fish, which have skeletons primarily composed of . Chondrichthyes are with , paired , , in the , and a lack of opercula and . Within the infraphylum , cartilaginous fishes are distinct from all other jawed vertebrates.

The class is divided into two subclasses: (, , skates and ) and (, 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 .


Anatomy

Skeleton
The skeleton is cartilaginous. The is gradually replaced by a vertebral column during development, except in , where the notochord stays intact. In some deepwater sharks, the column is reduced.
(2001). 9789251045435, Food & Agriculture Org.. .

As they do not have , red blood cells are produced in the 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 , which is a very specialized group, lacks both the Leydig's and epigonal organs.


Appendages
Apart from , 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 (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 , 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.


Body covering
Chondrichthyans have tooth-like scales called 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 bony fish Denticeps clupeoides has most of its head covered by dermal teeth (as does, probably, , 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 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.


Respiratory system
All chondrichthyans breathe through five to seven pairs of , 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
In chondrichthyans, the nervous system is composed of a small brain, 8–10 pairs of cranial nerves, and a spinal cord with spinal nerves. They have several sensory organs which provide information to be processed. Ampullae of Lorenzini are a network of small jelly filled pores called which help the fish sense electric fields in water. This aids in finding prey, navigation, and sensing temperature. The 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 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.


Immune system
Like all other jawed vertebrates, members of Chondrichthyes have an adaptive immune system.


Reproduction
Fertilization is internal. Development is usually live birth ( species) but can be through eggs (). Some rare species are . 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. 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).


Classification
The class Chondrichthyes has two subclasses: the subclass (, ) and the subclass (). To see the full list of the species, click here.

, 1977851>27071021
, 1940119
, 19587
+2 extinct
1016 10
Applegate, 197271343 7
de Buen, 19262
+3 extinct
4
+11 extinct
7
+33 extinct
, 1958126
Goodrich, 19097231261 6
Buen, 19261124345
Compagno, 1973102922311633
125–75–7
, 1940536>27041226
de Buen, 1926212692 9
, 19533
+2 extinct
6
+3 extinct
39
+17 extinct

  • †Order Mongolepidiformes Karatajüte-Talimaa & Novitskaya, 1990
  • †Order Turner, 1997
  • †Order Coronodontiformes Zangerl, 1981
  • †Order Zangerl, 1981
  • Subclass
    • †Superorder Paraselachimorpha
      • †Order Desmiodontiformes Zangerl, 1981
      • †Order Polysentoriformes Cappetta, 1993
      • †Order Zangerl, 1981
      • †Order Petalodontiformes Zangerl, 1981
      • †Order Patterson, 1965
      • †Order Iniopterygiformes Zanger, 1973
      • †Order Grogan & Lund, 2000
      • †Order Eugeneodontiformes Zangerl, 1981
    • Superorder Holocephalimorpha
      • †Order Psammodontiformes* Obruchev, 1953
      • †Order Obručhev, 1953
      • †Order
      • †Order Chondrenchelyiformes Moy-Thomas, 1939
      • †Order
      • †Order Cochliodontiformes Obručhev, 1953
      • Order Berg, 1940 sensu Obručhev, 1953 (chimaeras)
  • Subclass
    • †Order Antarctilamniformes Ginter, Liao & Valenzuela-Rios, 2008
    • †Order Elegestolepidiformes Andreev et al., 2016
    • †Order Karatajute-Talimaa, 1997
    • †Order Squatinactiformes Zangerl, 1981
    • †Order Protacrodontiformes Zangerl, 1981
    • †Infraclass Cladoselachimorpha
      • †Order Cladoselachiformes Dean, 1909
    • †Infraclass Xenacanthimorpha Berg, 1940
      • †Order Bransonelliformes Hampe & Ivanov, 2007
      • †Order Berg, 1940
    • Infraclass Euselachii (sharks and rays)
      • †Order Altholepidiformes Andreev et al., 2015
      • †Order Polymerolepidiformes
      • †Order Ptychodontiformes
      • †Order Ctenacanthiformes Zangerl, 1981
      • †Division Hybodonta
      • Division Neoselachii Compagno, 1977
        • Subdivision Selachii (modern sharks)
          • Superorder Galeomorphi Compagno, 1977
            • Order Heterodontiformes (bullhead sharks)
            • Order (carpet sharks)
            • Order (mackerel sharks)
            • Order Carcharhiniformes (ground sharks)
          • Superorder Squalomorphi
            • Order Chlamydoselachiformes
            • Order (frilled and cow sharks)
            • Order (dogfish sharks)
            • †Order Protospinaciformes
            • †Order Synechodontiformes
            • Order (angel sharks)
            • Order Pristiophoriformes (sawsharks)
        • Subdivision Batoidea
* position uncertain


Evolution
Cartilaginous fish are considered to have evolved from . The discovery of 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. In particular, new phylogenetic studies find cartilaginous fish to be well nested among acanthodians, with and being the closest relatives to Chondrichthyes. Recent studies vindicate this, as had a mosaic of chondrichthyan and acanthodian traits. Dating back to the Middle and Late Period, many isolated scales, made of and bone, have a structure and growth form that is chondrichthyan-like. They may be the remains of -chondrichthyans, but their classification remains uncertain.

The earliest unequivocal fossils of acanthodian-grade cartilaginous fishes are and from the early Silurian () of , 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 and early cartilaginous fish. The modern bony fishes, class , appeared in the late or early Devonian, about 416 million years ago. The first abundant genus of shark, , appeared in the oceans during the Devonian Period. The first cartilaginous fishes evolved from -like ancestors.

PetalodontsZangerl, 19814 Members of the holocephali, some genera resembled parrot fish, but some members of the resembled skates.
Members of the holocephali that resembled flying fish, are often characterized by large eyes, large upturned pectoral fins, and club-like tails.
Zangerl, 1981 (sensu Maisey, 2007)4 Members of the holocephali, they were heavily sexually dimorphic.
Eugeneodontida Zangerl, 19814 Members of the holocephali, they are characterized by large tooth whorls in their jaws.
Position uncertain
Other Cappetta et al., 199311
Dean, 189412 Holocephalans, and potential members of the symmoriida.
Glikman, 19644 Eel-like elasmobranchs that were some of the top freshwater predators of the late Paleozoic.
CtenacanthsGlikman, 19642 Shark-like elasmobranchs characterized by their robust heads and large dorsal fin spines.
Patterson, 19665 Shark-like elasmobranchs distinguished by their conical tooth shape, and the presence of a spine on each of their two dorsal fins.


Taxonomy
Subphylum '''[[Vertebrata]]'''
└─'''Infraphylum Gnathostomata'''
      ├─[[Placodermi]] — ''extinct'' (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
  • List of cartilaginous fish
  • Cartilaginous versus bony fishes
  • Largest cartilaginous fishes
  • Important Shark and Ray Areas (ISRA)
  • Threatened sharks


Further reading

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