Eusuchia
Eusuchia Temporal range: Early Cretaceous - Recent,
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Three species of living eusuchian: gharial (left), American alligator (center), and American crocodile (right). | |||
Scientific classification | |||
Domain: | Eukaryota | ||
Kingdom: | Animalia | ||
Phylum: | Chordata | ||
Class: | Reptilia | ||
Clade: | Archosauria | ||
Clade: | Pseudosuchia | ||
Clade: | Crocodylomorpha | ||
Clade: | Crocodyliformes | ||
Clade: | Neosuchia | ||
Clade: | Eusuchia Huxley, 1875 | ||
Subgroups | |||
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Eusuchia is a clade of neosuchian crocodylomorphs that first appeared in the Early Cretaceous, which includes modern crocodilians.[8] Along with Dyrosauridae and Sebecosuchia, they were the only crocodyliformes who survived the K-Pg extinction.
Definition
[edit]Eusuchia was originally defined by Thomas Henry Huxley in 1875 as an apomorphy-based group, meaning that it was defined by shared characteristics rather than relations. These characteristics include pterygoid-bounded choanae and vertebrae which are procoelous (concave from the front and convex from the back). The possibility that these traits may have been convergently evolved in different groups of neosuchians rather than one lineage spurred some modern paleontologists to revise the group's definition to make it defined solely by relations. In 1999, Christopher Brochu redefined Eusuchia as "the last common ancestor of Hylaeochampsa and Crocodylia and all of its descendants".[9] In this definition, "Crocodylia" specifically refers to descendants of the common ancestor of the three modern lineages of eusuchians: Gavialoidea (gharials), Alligatoroidea (alligators and caimans), and Crocodyloidea (crocodiles). Whether certain families or genera qualify as basal eusuchians or non-eusuchian neosuchians is a matter of debate over which definition is used for the group. At least one genus, Isisfordia, would qualify as a eusuchian under Huxley's definition of the group but would not necessarily qualify under Brochu's definition.
Description
[edit]Unlike primitive crocodylomorphs, crocodyliforms have secondary bony palates. This feature enables living crocodylians to safely breathe in through their nostrils while the rest of the head (including the mouth) remains submerged. This structure reaches its greatest elaboration among eusuchians, in which the internal nares are completely surrounded by the pterygoid bones.
Unlike more basal neosuchians, eusuchians have four rather than two rows of dorsal armour plates, which are square in shape, with 2 to 4 rows of accessory plates.[10]
Phylogeny
[edit]A 2018 tip dating study by Lee & Yates using both molecular, morphological and stratigraphic data recovered the cladogram below:[3]
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A 2021 Rio & Mannion phylogenetic study using a heavily modified morphological data set recovered the cladogram below:[11]
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References
[edit]- ^ a b c d White, M.A.; Bell, P.R.; Campione, N.E.; Sansalone, G.; Brougham, T.; Bevitt, J.J.; Molnar, R.E.; Cook, A.G.; Wroe, S.; Elliott, D.A. (2022). "Abdominal contents reveal Cretaceous crocodyliforms ate dinosaurs". Gondwana Research. 106: 281–302. Bibcode:2022GondR.106..281W. doi:10.1016/j.gr.2022.01.016.
- ^ Casey M. Holliday & Nicholas M. Gardner (2012). "A New Eusuchian Crocodyliform with Novel Cranial Integument and Its Significance for the Origin and Evolution of Crocodylia". PLOS ONE. 7 (1): e30471. Bibcode:2012PLoSO...730471H. doi:10.1371/journal.pone.0030471. PMC 3269432. PMID 22303441.
- ^ a b Michael S. Y. Lee; Adam M. Yates (27 June 2018). "Tip-dating and homoplasy: reconciling the shallow molecular divergences of modern gharials with their long fossil". Proceedings of the Royal Society B. 285 (1881). doi:10.1098/rspb.2018.1071. PMC 6030529. PMID 30051855.
- ^ Fachini, T.S.; Godoy, P.L.; Marsola, J.C.A.; Montefeltro, F.C.; Langer, M.C. (2022). "A large-sized mesoeucrocodylian from the Late Cretaceous of Brazil with possible neosuchian affinities". Historical Biology. 35 (10): 1817–1830. doi:10.1080/08912963.2022.2122822.
- ^ Noto, Christopher R.; Drumheller, Stephanie K.; Adams, Thomas L.; Turner, Alan H. (2020). "An Enigmatic Small Neosuchian Crocodyliform from the Woodbine Formation of Texas". The Anatomical Record. 303 (4): 801–812. doi:10.1002/ar.24174. ISSN 1932-8494. PMID 31173481.
- ^ a b Schwarz, D.; Raddatz, M.; Wings, O. (2017). "Knoetschkesuchus langenbergensis gen. nov. sp. nov., a new atoposaurid crocodyliform from the Upper Jurassic Langenberg Quarry (Lower Saxony, northwestern Germany), and its relationships to Theriosuchus". PLOS ONE. 12 (2): e0160617. Bibcode:2017PLoSO..1260617S. doi:10.1371/journal.pone.0160617. PMC 5310792. PMID 28199316.
- ^ Noto, Christopher R.; Drumheller, Stephanie K.; Adams, Thomas L.; Turner, Alan H. (2020). "An Enigmatic Small Neosuchian Crocodyliform from the Woodbine Formation of Texas". The Anatomical Record. 303 (4): 801–812. doi:10.1002/ar.24174. ISSN 1932-8494. PMID 31173481.
- ^ Benton, Michael J.; Sibbick, John (2000). Vertebrate Palaeontology. Blackwell Publishing. p. 233. ISBN 0-632-05614-2.
- ^ Brochu, Christopher A. (2003). "PHYLOGENETIC APPROACHES TOWARD CROCODYLIAN HISTORY". Annual Review of Earth and Planetary Sciences (31): 357–97. doi:10.1146/annurev.earth.31.100901.141308.
- ^ Puértolas-Pascual, E; Mateus, O (2020-06-11). "A three-dimensional skeleton of Goniopholididae from the Late Jurassic of Portugal: implications for the Crocodylomorpha bracing system". Zoological Journal of the Linnean Society. 189 (2): 521–548. doi:10.1093/zoolinnean/zlz102. ISSN 0024-4082.
- ^ Rio, Jonathan P.; Mannion, Philip D. (6 September 2021). "Phylogenetic analysis of a new morphological dataset elucidates the evolutionary history of Crocodylia and resolves the long-standing gharial problem". PeerJ. 9: e12094. doi:10.7717/peerj.12094. PMC 8428266. PMID 34567843.