Elasmobranchii Explained

Elasmobranchii is a subclass of Chondrichthyes or cartilaginous fish, including modern sharks (superorder Selachii), rays, skates, and sawfish (superorder Batoidea). Members of this subclass are characterised by having five to seven pairs of gill clefts opening individually to the exterior, rigid dorsal fins and small placoid scales on the skin. 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 details of this jaw anatomy vary between species, and help distinguish the different elasmobranch clades. The pelvic fins in males are modified to create claspers for the transfer of sperm. There is no swim bladder; instead, these fish maintain buoyancy with large livers rich in oil.

The definition of the clade is unclear with respect to fossil chondrichthyans. Some authors consider it as equivalent to Neoselachii (the crown group clade including modern sharks, rays, and all other descendants of their last common ancestor). Other authors use the name Elasmobranchii for a broader branch-based group of all chondrichthyans more closely related to modern sharks and rays than to Holocephali (the clade containing chimaeras and their extinct relatives).[1] Important extinct groups of elasmobranchs sensu lato include the hybodonts (Order Hybodontiformes), xenacanths (order Xenacanthformes) and Ctenacanthiformes. These are also often referred to as "sharks" in reference to their similar anatomy and ecology to modern sharks.

The name Elasmobranchii comes from the Ancient Greek words ("plate") and ("gill"), referring to the broad, flattened gills which are characteristic of these fishes.

Description

Elasmobranchii is one of the two subclasses of cartilaginous fish in the class Chondrichthyes, the other being Holocephali (chimaeras).

Members of the elasmobranchii subclass 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.

Extant elasmobranchs exhibit several archetypal jaw suspensions: amphistyly, orbitostyly, hyostyly, and euhyostyly. In amphistyly, the palatoquadrate has a postorbital articulation with the chondrocranium from which ligaments primarily suspend it anteriorly. The hyoid articulates with the mandibular arch posteriorly, but it appears to provide little support to the upper and lower jaws. In orbitostyly, the orbital process hinges with the orbital wall and the hyoid provides the majority of suspensory support.

In contrast, hyostyly involves an ethmoid articulation between the upper jaw and the cranium, while the hyoid most likely provides vastly more jaw support compared to the anterior ligaments. Finally, in euhyostyly, also known as true hyostyly, the mandibular cartilages lack a ligamentous connection to the cranium. Instead, the hyomandibular cartilages provide the only means of jaw support, while the ceratohyal and basihyal elements articulate with the lower jaw, but are disconnected from the rest of the hyoid.[2] [3] [4] 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.[5]

Many fish maintain buoyancy with swim bladders. However elasmobranchs lack swim bladders, and maintain buoyancy instead with large livers that are full of oil.[6] This stored oil may also function as a nutrient when food is scarce.[7] [8]

Evolutionary history

See also: Evolution of fish. The oldest unambigous total group elasmobranch, Phoebodus, has its earliest records in the Middle Devonian (late Givetian), around 383 million years ago.[9] Several important groups of total group elasmobranchs, including Ctenacanthiformes and Hybodontiformes, had already emerged by the latest Devonian (Famennian).[10] During the Carboniferous, some ctenacanths would grow to sizes rivalling the modern great white shark with bodies in the region of 7m (23feet) in length.[11] During the Carboniferous and Permian, the xenacanths were abundant in both freshwater and marine environments, and would continue to exist into the Triassic with reduced diversity.[12] The hybodonts had achieved a high diversity by the Permian,[13] and would end up becoming the dominant group of elasmobranchs during the Triassic and Early Jurassic. Hybodonts were extensively present in both marine and freshwater environments.[14] While Neoselachii/Elasmobranchi sensu stricto (the group of modern sharks and rays) had already appeared by the Triassic, they only had low diversity during this period would and only begin to extensively diversify from the Early Jurassic onwards, when modern orders of sharks and rays appeared.[15] This co-incided with the decline of the hybodonts, which had become minor components of marine environments by the Late Jurassic, but would remain common in freshwater environments into the Cretaceous.[16] The youngest remains of hybodonts date to the very end of the Cretaceous.[17]

Taxonomy

Elasmobranchii was first coined in 1838 by Charles Lucien Bonaparte. Bonaparte's original definition of Elasmobranchii was effectively identical to modern Chondrichthyes, and was based around gill architecture shared by all 3 living major cartilaginous fish groups. During the 20th century it became standard to exclude chimaeras from Elasmobranchii; along with including many fossil chondrichthyans within the group. The definition of Elasmobranchii has since been subject to much confusion with regard to fossil chondrichthyans. Maisey (2012) suggested that Elasmobranchii should exclusively be used for the last common ancestor of modern sharks and rays, a grouping which had previously been named Neoselachii by Compagno (1977). Other recent authors have used Elasmobranchii in a broad sense to include all chondrichthyans more closely related to modern sharks and rays than to chimaeras.

The total group of Elasmobranchii includes the Cohort Euselachii Hay, 1902, which groups the Hybodontiformes and a number of other extinct chondrichthyans with Elasmobrachii sensu stricto/Neoselachii, to the exclusion of more primitive total group elasmobranchs, which is supported by a number of shared morphological characters of the skeleton.[18] [19] [20] [21]

Recent molecular studies suggest the Batoidea are not derived selachians as previously thought. Instead, skates and rays are a monophyletic superorder within Elasmobranchii that shares a common ancestor with the selachians.[24] [25]

See also

External links

Notes and References

  1. Maisey . J. G. . April 2012 . What is an 'elasmobranch'? The impact of palaeontology in understanding elasmobranch phylogeny and evolution . Journal of Fish Biology . en . 80 . 5 . 918–951 . 10.1111/j.1095-8649.2012.03245.x. 22497368 . 2012JFBio..80..918M .
  2. 10.1002/jmor.10342 . 15880740 . Morphology and evolution of the jaw suspension in lamniform sharks . Journal of Morphology . 265 . 1 . 102–19 . 2005 . Wilga . C.D. . 45227734 .
  3. 10.1093/icb/icm029 . 21672820 . Evolution and ecology of feeding in elasmobranchs . Integrative and Comparative Biology . 47 . 1 . 55–69 . 2007 . Wilga . C. D. . Motta . P. J. . Sanford . C. P. . free .
  4. Wilga . Cheryl A.D. . 2008 . Evolutionary divergence in the feeding mechanism of fishes . Acta Geologica Polonica . 58 . 2 . 113–20 . 2017-05-24 . https://web.archive.org/web/20180819031736/https://geojournals.pgi.gov.pl/agp/article/view/9981 . 2018-08-19 . live .
  5. Book: Bigelow, Henry B. . Henry Bryant Bigelow. Schroeder, William C.. Fishes of the Western North Atlantic . Sears Foundation for Marine Research, Yale University . 1948 . 64–65 . B000J0D9X6.
  6. Oguri, M (1990) "A review of selected physiological characteristics unique to elasmobranchs" In: Elasmobranchs as living resources: advances in the biology, ecology, systematics and the status of the fisheries, eds. J. H. L. Pratt, S. H. Gruber and T. Taniuchi, US Department of Commerce, NOAA technical report NMFS 90, pp.49–54.
  7. Hoenig, J.M. and Gruber, S.H. (1990) "Life-history patterns in the elasmobranchs: implications for fisheries management" In: Elasmobranchs as living resources: advances in the biology, ecology, systematics and the status of the fisheries, eds. J. H. L. Pratt, S. H. Gruber and T. Taniuchi, US Department of Commerce, NOAA technical report NMFS 90, pp.1–16.
  8. 10.1017/S0025315400038017 . The density of elasmobranchs . Journal of the Marine Biological Association of the United Kingdom . 49 . 4 . 913 . 2009 . Bone . Q. . Roberts . B. L. . 85871565 .
  9. Frey . Linda . Coates . Michael . Ginter . Michał . Hairapetian . Vachik . Rücklin . Martin . Jerjen . Iwan . Klug . Christian . 2019-10-09 . The early elasmobranch Phoebodus : phylogenetic relationships, ecomorphology and a new time-scale for shark evolution . Proceedings of the Royal Society B: Biological Sciences . en . 286 . 1912 . 20191336 . 10.1098/rspb.2019.1336 . 0962-8452 . 6790773 . 31575362.
  10. Schultze, H.-P., Bullecks, J., Soar, L. K., & Hagadorn, J. (2021). Devonian fish from Colorado’s Dyer Formation and the appearance of Carboniferous faunas in the Famennian. In A. Pradel, J. S. S. Denton, & P. Janvier (Eds.), Ancient Fishes and their Living Relatives: a Tribute to John G. Maisey (pp. 247–256.). Verlag Dr. Friedrich Pfeil.
  11. Maisey . John G. . Bronson . Allison W. . Williams . Robert R. . McKinzie . Mark . 2017-05-04 . A Pennsylvanian 'supershark' from Texas . Journal of Vertebrate Paleontology . en . 37 . 3 . e1325369 . 10.1080/02724634.2017.1325369 . 2017JVPal..37E5369M . 134127771 . 0272-4634.
  12. Pauliv . Victor E. . Martinelli . Agustín G. . Francischini . Heitor . Dentzien-Dias . Paula . Soares . Marina B. . Schultz . Cesar L. . Ribeiro . Ana M. . December 2017 . The first Western Gondwanan species of Triodus Jordan 1849: A new Xenacanthiformes (Chondrichthyes) from the late Paleozoic of Southern Brazil . Journal of South American Earth Sciences . en . 80 . 482–493 . 10.1016/j.jsames.2017.09.007. 2017JSAES..80..482P .
  13. Koot . Martha B. . Cuny . Gilles . Tintori . Andrea . Twitchett . Richard J. . March 2013 . A new diverse shark fauna from the Wordian (Middle Permian) Khuff Formation in the interior Haushi-Huqf area, Sultanate of Oman . Palaeontology . en . 56 . 2 . 303–343 . 10.1111/j.1475-4983.2012.01199.x . 2013Palgy..56..303K . 86428264 . 0031-0239.
  14. Rees, J. A. N., and Underwood, C. J., 2008, Hybodont sharks of the English Bathonian and Callovian (Middle Jurassic): Palaeontology, v. 51, no. 1, p. 117-147.
  15. Underwood . Charlie J. . March 2006 . Diversification of the Neoselachii (Chondrichthyes) during the Jurassic and Cretaceous . Paleobiology . en . 32 . 2 . 215–235 . 2006Pbio...32..215U . 10.1666/04069.1 . 0094-8373 . 86232401.
  16. Rees . Jan . Underwood . Charlie J. . January 2008 . Hybodont Sharks of the English Bathonian and Callovian (Middle Jurassic) . Palaeontology . en . 51 . 1 . 117–147 . 10.1111/j.1475-4983.2007.00737.x . 0031-0239. free . 2008Palgy..51..117R .
  17. Carrillo-Briceño . Jorge D. . Cadena . Edwin A. . Dececchi . Alex T. . Larson . Hans C. E. . Du . Trina Y. . 2016-01-01 . First record of a hybodont shark (Chondrichthyes: Hybodontiformes) from the Lower Cretaceous of Colombia . Neotropical Biodiversity . en . 2 . 1 . 81–86 . 10.1080/23766808.2016.1191749 . 2016NeBio...2...81C . 2376-6808.
  18. Maisey . John G. . March 2011 . The braincase of the Middle Triassic shark Acronemus tuberculatus (Bassani, 1886) . Palaeontology . en . 54 . 2 . 417–428 . 10.1111/j.1475-4983.2011.01035.x . 2011Palgy..54..417M . 140697673 . 0031-0239.
  19. Coates . Michael I. . Tietjen . Kristen . March 2017 . The neurocranium of the Lower Carboniferous shark Tristychius arcuatus (Agassiz,) . Earth and Environmental Science Transactions of the Royal Society of Edinburgh . en . 108 . 1 . 19–35 . 10.1017/S1755691018000130 . 2017EESTR.108...19C . 135297534 . 1755-6910.
  20. Villalobos-Segura . Eduardo . Stumpf . Sebastian . Türtscher . Julia . Jambura . Patrick . Begat . Arnaud . López-Romero . Faviel . Fischer . Jan . Kriwet . Jürgen . 2023-03-08 . A Synoptic Review of the Cartilaginous Fishes (Chondrichthyes: Holocephali, Elasmobranchii) from the Upper Jurassic Konservat-Lagerstätten of Southern Germany: Taxonomy, Diversity, and Faunal Relationships . Diversity . en . 15 . 3 . 386 . 10.3390/d15030386 . free . 1424-2818 . 7614348 . 36950327.
  21. Luccisano . Vincent . Rambert-Natsuaki . Mizuki . Cuny . Gilles . Amiot . Romain . Pouillon . Jean-Marc . Pradel . Alan . 2021-12-02 . Phylogenetic implications of the systematic reassessment of Xenacanthiformes and 'Ctenacanthiformes' (Chondrichthyes) neurocrania from the Carboniferous–Permian Autun Basin (France) . Journal of Systematic Palaeontology . en . 19 . 23 . 1623–1642 . 10.1080/14772019.2022.2073279 . 2021JSPal..19.1623L . 1477-2019.
  22. Book: Ebert . David A. . Sharks of the world: a complete guide . Fowler . Sarah . Dando . Marc . 2021 . Princeton University Press . 978-0-691-20599-1 . Princeton.
  23. Web site: WoRMS - World Register of Marine Species - Echinorhiniformes . 2022-01-04.
  24. 10.1016/j.ympev.2003.07.010 . 15019621 . Phylogeny of elasmobranchs based on LSU and SSU ribosomal RNA genes . Molecular Phylogenetics and Evolution . 31 . 1 . 214–24 . 2004 . Winchell . Christopher J . Martin . Andrew P . Mallatt . Jon .
  25. 10.1016/S1055-7903(02)00333-0 . 12565032 . Molecular phylogenetic evidence refuting the hypothesis of Batoidea (rays and skates) as derived sharks . Molecular Phylogenetics and Evolution . 26 . 2 . 215–21 . 2003 . Douady . Christophe J. . Dosay . Miné . Shivji . Mahmood S. . Stanhope . Michael J. .

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