Chondrichthyes

Chondrichthyes (/kɒnˈdrɪkθi.z/; from Ancient Greek χόνδρος (khóndros) 'cartilage', and ἰχθύς (ikhthús) 'fish') is a class that contains the cartilaginous fishes that have skeletons primarily composed of cartilage. They can be contrasted with the Osteichthyes or bony fishes, which have skeletons primarily composed of bone tissue. Chondrichthyes are jawed vertebrates with paired fins, paired nares, scales, and a heart with its chambers in series. Extant chondrichthyes range in size from the 10 cm (3.9 in) finless sleeper ray to the 10 m (32 ft) whale shark.

Cartilaginous fishes
Temporal range: Late Silurian to Present
Example of cartilaginous fishes: Elasmobranchii at the top of the image and Holocephali at the bottom of the image.
Scientific classification
Kingdom: Animalia
Phylum: Chordata
Subphylum: Vertebrata
Infraphylum: Gnathostomata
Clade: Eugnathostomata
Class: Chondrichthyes
Huxley, 1880
Living subclasses and orders
  • Subclass Elasmobranchii
  • Subclass Holocephali
    • Superorder Holocephalimorpha
      • Order Chimaeriformes

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).

Within the infraphylum Gnathostomata, cartilaginous fishes are distinct from all other jawed vertebrates.

Anatomy

Skeleton

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.[3]

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

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.[4]

Body covering

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 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 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

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 chord with spinal nerves.[5] 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.[6]

Immune system

Like all other jawed vertebrates, members of Chondrichthyes have an adaptive immune system.[7]

Reproduction

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.[8] 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).[8]

Classification

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.[9]
Holocephali
Chimaeras
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

Radiation of cartilaginous fishes, based on Michael Benton, 2005.[12]

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.[13] In particular, new phylogenetic studies find cartilaginous fish to be well nested among acanthodians, with Doliodus and Tamiobatis being the closest relatives to Chondrichthyes.[14] Recent studies vindicate this, as Doliodus had a mosaic of chondrichthyan and acanthodian traits.[15] A lower Silurian taxon, Fanjingshania renovata[16], assigned to Climatiiformes[16] is the oldest chondrichthyan with known anatomical features.

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.[17][18][19]

The earliest unequivocal fossils of cartilaginous fishes first appeared in the fossil record by about 430 million years ago, during the middle Wenlock Epoch of the Silurian period.[20] The radiation of elasmobranches in the chart on the right is divided into the taxa: Cladoselache, Eugeneodontiformes, Symmoriida, Xenacanthiformes, Ctenacanthiformes, Hybodontiformes, Galeomorphi, Squaliformes and Batoidea.

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
†Helodontiformes
†Iniopterygiformes
†Debeeriiformes
†Symmoriida [21]
†Eugeneodontida [22]
†Psammodonti-
formes
Position uncertain
†Copodontiformes
†Squalorajiformes
†Chondrenchelyi-
formes
†Menaspiformes
†Cochliodontiformes
Squalomorph
sharks
†Protospinaci-
formes
Other †Squatinactiformes
†Protacrodonti-
formes
†Cladoselachi-
formes
†Xenacanthiformes
†Ctenacanthi-
formes
†Hybodontiformes

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

References

  1. Botella, H.A.; Donoghue, P.C.J.; Martínez-Pérez, C. (2009). "Enameloid microstructure in the oldest known chondrichthyan teeth". Acta Zoologica. 90 (Supplement): 103–108. doi:10.1111/j.1463-6395.2008.00337.x.
  2. "Chondrichthyes". PalaeoDB. Retrieved 26 November 2013.
  3. Sharks of the World: An Annotated and Illustrated Catalogue of Shark Species Known to Date
  4. Wilga, C. D.; Lauder, G. V. (2002). "Function of the heterocercal tail in sharks: quantitative wake dynamics during steady horizontal swimming and vertical maneuvering". Journal of Experimental Biology. 205 (16): 2365–2374. doi:10.1242/jeb.205.16.2365. PMID 12124362.
  5. Collin, Shaun P. (2012). "The Neuroecology of Cartilaginous Fishes: Sensory Strategies for Survival". Brain, Behavior and Evolution. 80 (2): 80–96. doi:10.1159/000339870. ISSN 1421-9743. PMID 22986825. S2CID 207717002.
  6. de Bellard, Maria Elena (15 June 2016). "Myelin in cartilaginous fish". Brain Research. 1641 (Pt A): 34–42. doi:10.1016/j.brainres.2016.01.013. ISSN 0006-8993. PMC 4909530. PMID 26776480.
  7. Flajnik, M. F.; Kasahara, M. (2009). "Origin and evolution of the adaptive immune system: genetic events and selective pressures". Nature Reviews Genetics. 11 (1): 47–59. doi:10.1038/nrg2703. PMC 3805090. PMID 19997068.
  8. Adams, Kye R.; Fetterplace, Lachlan C.; Davis, Andrew R.; Taylor, Matthew D.; Knott, Nathan A. (January 2018). "Sharks, rays and abortion: The prevalence of capture-induced parturition in elasmobranchs". Biological Conservation. 217: 11–27. doi:10.1016/j.biocon.2017.10.010. S2CID 90834034. Archived from the original on 23 February 2019. Retrieved 18 January 2019.
  9. Bigelow, Henry B.; Schroeder, William C. (1948). Fishes of the Western North Atlantic. Sears Foundation for Marine Research, Yale University. pp. 64–65. ASIN B000J0D9X6.
  10. Leonard Compagno (2005) Sharks of the World. ISBN 9780691120720.
  11. Haaramo, Mikko. Chondrichthyes – Sharks, Rays and Chimaeras. Retrieved 22 October 2013.
  12. Benton, M. J. (2005). Vertebrate Palaeontology (3rd ed.). Blackwell. Fig 7.13 on page 185. ISBN 978-0-632-05637-8.
  13. Min Zhu; Xiaobo Yu; Per Erik Ahlberg; Brian Choo; Jing Lu; Tuo Qiao; Qingming Qu; Wenjin Zhao; Liantao Jia; Henning Blom; You'an Zhu (2013). "A Silurian placoderm with osteichthyan-like marginal jaw bones". Nature. 502 (7470): 188–193. Bibcode:2013Natur.502..188Z. doi:10.1038/nature12617. PMID 24067611. S2CID 4462506.
  14. Burrow, CJ; Den Blaauwen, J.; Newman, MJ; Davidson, RG (2016). "The diplacanthid fishes (Acanthodii, Diplacanthiformes, Diplacanthidae) from the Middle Devonian of Scotland". Palaeontologia Electronica. doi:10.26879/601.
  15. 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.
  16. Andreev, P.S.; Sansom, I.J.; Li, Q.; Zhao, W.; Wang, J.; Wang, C.C.; Peng, L.; Jia, L.; Qiao, T.; Zhu, M. (2022). "Spiny chondrichthyan from the lower Silurian of South China". Nature. 609 (7929): 969–974. doi:10.1038/s41586-022-05233-8.
  17. 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.
  18. 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. doi:10.1111/j.1475-4983.2012.01127.x.
  19. 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.
  20. Märss, Tiiu; Gagnier, Pierre-Yves (2001). "A new chondrichthyan from the Wenlock, Lower Silurian, of Baillie-Hamilton Island, the Canadian Arctic". Journal of Vertebrate Paleontology. 21 (4): 693–701. doi:10.1671/0272-4634(2001)021[0693:ANCFTW]2.0.CO;2. S2CID 86329421.
  21. 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.
  22. Tapanila, L; Pruitt, J; Pradel, A; Wilga, C; Ramsay, J; Schlader, R; Didier, D (2013). "Jaws for a spiral-tooth whorl: CT images reveal novel adaptation and phylogeny in fossil Helicoprion". Biology Letters. 9 (2): 20130057. doi:10.1098/rsbl.2013.0057. PMC 3639784. PMID 23445952.

Further reading

This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.