Hybodontiformes

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Hybodontiformes
Temporal range: 360.7–66 Ma Late Devonian to Late Cretaceous
Asteracanthus image.jpg
Fossil and life restoration of Asteracanthus, from the Late Jurassic of Europe
Scientific classification e
Kingdom: Animalia
Phylum: Chordata
Clade: Eugnathostomata
Class: Chondrichthyes
Subclass: Elasmobranchii
Order: †Hybodontiformes
Patterson, 1966
Families

Hybodontiformes, commonly called hybodonts, are an extinct group of shark-like chondrichthyans, which existed from the late Devonian to the Late Cretaceous. They form the group of Elasmobranchii closest to neoselachians, the clade of modern sharks and rays. Hybodonts were named and are distinguished based on their conical tooth shape. They are also noted for the presence of a spine on each of their two dorsal fins. They were abundant in marine and freshwater environments during the late Paleozoic and early Mesozoic, but were rare in open marine environments by the end of the Jurassic, having been largely replaced by modern sharks, though they were still common in freshwater and marginal marine habitats. They survived until the end of the Cretaceous, before going extinct.

Radiation of cartilaginous fishes, including the Hybodontiformes. Derived from work by Michael Benton, 2005.[1]

Etymology

The term hybodont comes from the Greek word ὕβος or ὑβός meaning hump or hump-backed and ὀδούς, ὀδοντ meaning tooth. This name was given based on their conical compressed teeth.

Taxonomic history

Hybodonts were first described in the nineteenth century based on isolated fossil teeth (Agassiz, 1837). Hybodonts were first separated from living sharks by Zittel (1911).[2] Hybodontiformes are a type of elasmobranch, and the sister group to Neoselachii. Hybodontiformes are classified in the Euselachii along with Xenacanthiformes, Ctenacanthiformes and Neoselachii. Hybodonts are divided into a number of families, including Hybodontidae, but the higher level taxonomy of hybodonts, especially Mesozoic taxa, is poorly resolved.[3]

Morphology and teeth

Specimen of Hybodus fraasi from the Late Jurassic of Germany

Hybodonts reached a maximum size of 2–3 metres (6.6–9.8 ft) in length, and had a relatively robust bodyform. Due to their cartilaginous skeletons usually disintergrating upon death like other chondrichthyans, hybodonts are generally described and identified based on size and shape of teeth and fin spine fossils, which are more likely to be preserved.[3] Rare complete skeletons are known from areas of exceptional preservation.[4][3][5]

Hybodonts are recognized as having teeth with a prominent cusp which is higher than lateral cusplets.[6] Hybodont teeth are often preserved as incomplete fossils because the base of the tooth is not well attached to the crown.[6] Hybodonts were initially divided into two groups based on their tooth shape.[7] One group had teeth with acuminate cusps that lacked a pulp cavity; these are called osteodont teeth. The other group had a different cusp arrangement and had a pulp cavity, these are called orthodont teeth.[8] For example, the hybodont species Heterophychodus steinmanni have osteodont teeth with vascular canals of dentine which are arranged vertically parallel to each other, also called ‘tubular dentine’.[9] The crowns of these osteodont teeth are covered with a single layer of enameloid. Hybodont teeth served a variety of functions depending on the species, including grinding, crushing (durophagy), tearing, clutching, and even cutting.[3]

Hybodonts are characterized by having two dorsal fins each preceded by a fin spine with a specific shape. The fin spines shape is used to distinguish hybodonts from other shark groups and different hybodont species.[10] The fin spines are elongate and gently curved toward the back of the animal.[10] Male hybodonts had small spines across their heads. Hybodonts had thick, massive jaws that vary between different genera according to diet and teeth.[11] Hybodonts had paired fins for steering and a fully heterocercal tail fin, where the upper lobe of the fin was much larger than the lower one due to the spine extending into it.

Evolutionary history

The earliest hybodont remains are from the latest Devonian (Famennian) of Iran, belonging to the genus Roongodus.[12] Although the first fossils of hybodonts are from the latest Devonian, they likely branched off from neoselachians (modern sharks) during the early Devonian.[13]

Life restoration of Strophodus rebecae with other contemporary organisms from the Early Cretaceous (Valanginian-Hauterivian) Rosa Blanca Formation of Colombia

Hybodont samples have been recovered from Permian deposits from Oman, indicating that hybodonts lived in the Neotethys Ocean during the Permian Period.[6] This study combined with others from Texas suggest that hybodonts were well established, and in some places dominant, during the Permian.[14] In general, the Permian record of hybodonts is limited. It was initially hypothesized that hybodont diversity was not significantly impacted by the end-Permian extinction, instead it was thought that diversity of Permian hybodonts declined over the 50 million years before the end-Permian extinction.[6] However, recent samples found in Oman suggests that Permian hybodont diversity extended until the end-Permian, suggesting the extinction was more impactful than previously thought.[6] Fossils from the Lower Triassic Vega-Phroso Siltstone Member of the Sulphur Mountain Formation of Alberta, Canada show well preserved specimens of Wapitiodus aplopagus which survived the extinction and was abundant in the Early Triassic.[15] Maximum hybodont diversity is observed during the Triassic. During the Triassic and Early Jurassic, hybodontiforms were the dominant selachians in both marine and non-marine environments.[16] A study of Middle Jurassic fossils from England analyzed 20 species from 11 genera suggesting that hybodonts flourished at that time.[16] A shift in hybodonts was seen during the Middle Jurassic, a transition between the distinctly different assemblages seen in the Triassic – Early Jurassic and the Late Jurassic – Cretaceous.[16] As neoselachians (group of modern sharks) diversified further during the Late Jurassic, hybodontiforms became less prevalent in open marine conditions but remained diverse in fluvial and restricted settings during the Cretaceous.[16] By the Cretaceous, hybodontiforms were primarily (though not solely) restricted to freshwater settings.[9] They remained successful during the Cretaceous by adapting to freshwater conditions, for example seven genera were found in freshwater deposits from Thailand.[9] The end-Cretaceous extinction of hybodont sharks may have been caused more by competition with other sharks than by the meteorite impact and volcanic eruptions cited to be the main cause of this extinction event.[17] Most other sharks were not significantly affected by the end-Cretaceous extinction, also suggesting that competition led to the demise of hybodonts.

Habitat

Hybodont teeth fossils are found in depositional environments ranging from marine to fluvial (river deposits). When they first evolved they inhabited both marine and freshwater systems. While hybodonts lived in freshwater throughout their existence, an example of hybodonts moving into more restricted conditions comes from Middle Jurassic samples found in lagoonal and other enclosed depositional settings.[16] Based on isotopic analysis, some species of hybodonts are likely to have permanently lived in freshwater environments,[18][19] while others may have migrated between marine and freshwater environments.[20]

Behavior

Hybodonts were likely slow swimmers and used their paired fins for steering and stabilization. Hybodus, a typical hybodontiform, was thought to be a slow swimmer but capable of occasional bursts on speed, making it an active predator of fast moving prey.[17] Hybodonts have a wide variety of tooth shapes. This variety suggests that they took advantage of multiple food sources.[6] It is thought that some hybodonts which had wider, flatter, teeth specialized in crushing hard-shelled prey (durophagy), evidence for this includes well-developed wear facets on teeth from Lissodus.[16] Species described from Thailand have a range of teeth shapes, suggesting multiple feeding habits. Bulbous teeth were used for crushing hard shelled bottom-dwelling prey.[21] Others were opportunistic feeders and were species that had a diet of large soft-bodied prey.[9] Little is known about the reproductive habits of hybodonts. One study found abundant fossil teeth and eggs sacks in freshwater lake deposits from the Triassic of Kyrgyzstan.[22] The site was interpreted as an ancient shark nursery based on the abundance of eggs and juvenile fossils and the limited number of adult specimens.[22]

References

  1. ^ Benton, M. J. (2005) Vertebrate Palaeontology, Blackwell, 3rd edition, Fig 7.13 on page 185.
  2. ^ Zittel, K. von, 1911, Grunzuege der Palaontologie, 2 ed. II. Abt. Vertebrata, vii + 598 pp. R. Oldenburg Verlag, Muchen, Berlin.
  3. ^ a b c d Stumpf, Sebastian; López‐Romero, Faviel A.; Kindlimann, René; Lacombat, Frederic; Pohl, Burkhard; Kriwet, Jürgen (August 2021). Cavin, Lionel (ed.). "A unique hybodontiform skeleton provides novel insights into Mesozoic chondrichthyan life". Papers in Palaeontology. 7 (3): 1479–1505. doi:10.1002/spp2.1350. ISSN 2056-2799.
  4. ^ Lane, J. A., and Maisey, J. G., 2009, Pectoral Anatomy of Tribodus limae (Elasmobranchii: Hybodontiformes) from the Lower Cretaceous of Northeastern Brazil: Journal of Vertebrate Paleontology, v. 29, no. 1, p. 25-38.
  5. ^ Wang, N.-Z.; Zhang, X.; Zhu, M.; Zhao, W.-J. (May 2009). "A new articulated hybodontoid from Late Permian of northwestern China". Acta Zoologica. 90: 159–170. doi:10.1111/j.1463-6395.2008.00382.x.
  6. ^ a b c d e f Koot, M. B., Cuny, G., Tintori, A., and Twitchett, R. J., 2013, A new diverse shark fauna from the Wordian (Middle Permian) Khuff Formation in the interior Haushi-Huqf area, Sultanate of Oman: Palaeontology, v. 56, no. 2, p. 303-343.
  7. ^ Agassiz, L., 1833-1844, Recherches sur les poisons fossils. Neuchatel, 5 vols. 1420 pp. with supplement.
  8. ^ Maisey, J. G., 1982, The anatomy and interrelationships of Mesozoic hybodont sharks: American Museum Novitates, v. 2724.
  9. ^ a b c d Cuny, G., Suteethorn, V., Buffetaut, E., and Philippe, M., 2003, Hybodont sharks from the Mesozoic Khorat Group of Thailand: Mahasarakham University Journal, v. 22.
  10. ^ a b Maisey, J. G., 1978, Growth and form of spines in hybodont sharks: Palaeontology, v. 21, no. 3, p. 657-666.
  11. ^ Carvalho, Marcelo, http://www.amnh.org/learn/sharks/Resource1
  12. ^ Hairapetian, V. and Ginter, M. 2009. Famennian chondrichthyan remains from the Chahriseh section, central Iran. Acta Geologica Polonica, 59, 173–200.
  13. ^ Coates, M. I., and Gess, R. W., 2007, A new reconstruction of Onychoselache Traquairi, comments on early Chondrichthyan pectoral girdles and hybodontiform phylogeny: Palaeontology, v. 50, no. 6, p. 1421-1446.
  14. ^ Koot, M. B., Cuny, G., Tintori, A., and Twitchett, R. J., 2013, A new diverse shark fauna from the Wordian (Middle Permian) Khuff Formatio in the interior Haushi-Huqf area, Sultanate of Oman: Palaeontology, v. 56, no. 2, p. 303-343.
  15. ^ Mutter, R. J., De Blanger, K., and Neuman, A. G., 2007, Elasmobranchs from the Lower Triassic Sulphur Mountain Formation near Wapiti Lake (BC, Canada): Zoological Journal of the Linnean Society, v. 149, no. 3, p. 309-337.
  16. ^ a b c d e f 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.
  17. ^ a b Maisey, J. G., 2012, What is an ‘elasmobranch’? The impact of palaeontology in understanding elasmobranch phylogeny and evolution: Journal of Fish Biology, v. 80, no. 5, p. 918-951.
  18. ^ Fischer, Jan; Schneider, Jörg W.; Voigt, Silke; Joachimski, Michael M.; Tichomirowa, Marion; Tütken, Thomas; Götze, Jens; Berner, Ulrich (2013-03-29). "Oxygen and strontium isotopes from fossil shark teeth: Environmental and ecological implications for Late Palaeozoic European basins". Chemical Geology. 342: 44–62. doi:10.1016/j.chemgeo.2013.01.022. ISSN 0009-2541.
  19. ^ Klug, Stefanie; Tütken, Thomas; Wings, Oliver; Pfretzschner, Hans-Ulrich; Martin, Thomas (2010-09-01). "A Late Jurassic freshwater shark assemblage (Chondrichthyes, Hybodontiformes) from the southern Junggar Basin, Xinjiang, Northwest China". Palaeobiodiversity and Palaeoenvironments. 90 (3): 241–257. doi:10.1007/s12549-010-0032-2. ISSN 1867-1608.
  20. ^ Leuzinger, L.; Kocsis, L.; Billon-Bruyat, J.-P.; Spezzaferri, S.; Vennemann, T. (2015-12-07). "Stable isotope study of a new chondrichthyan fauna (Kimmeridgian, Porrentruy, Swiss Jura): an unusual freshwater-influenced isotopic composition for the hybodont shark <i>Asteracanthus</i>". Biogeosciences. 12 (23): 6945–6954. doi:10.5194/bg-12-6945-2015. ISSN 1726-4189.
  21. ^ Cappetta, H., Buffetaut, E., Cuny, G., and Suteethorn, V., 2006, A new Elasmobranch assemblage from the Lower Cretaceous of Thailand Palaeontology, v. 49, no. 3, p. 547-555.
  22. ^ a b Fischer, J. A. N., Voigt, S., Schneider, J. W., Buchwitz, M., and Voigt, S., 2011, A selachian freshwater fauna from the Triassic of Kyrgyzstan and its implication for Mesozoic shark nurseries: Journal of Vertebrate Paleontology, v. 31, no. 5, p. 937-953.

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