Oudenodon

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Oudenodon
Temporal range: Late Permian
Oudenodon baini.jpg
O. baini skull at the Museum für Naturkunde, Berlin
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Suborder: Anomodontia
Clade: Dicynodontia
Family: Oudenodontidae
Genus: Oudenodon
Owen, 1860
Species
  • O. bainiiOwen, 1860 (type)
  • O. grandisHaughton, 1917
  • O. sakamenensisMazin and King, 1991
Synonyms
Genus synonymy
  • Chelyrhynchus Haughton, 1917
Species synonymy
  • Aulacocephalodon milletti(Broom, 1928)(originally Dicynodon milletti)
  • Chelyrhynchus lachrymalisHaughton, 1917
  • Dicynodon allaniBroom, 1940
  • Dicynodon andrewsiBroom, 1921
  • Dicynodon brachyrhynchusBroom, 1948
  • Dicynodon brevicepsHaughton, 1915
  • Dicynodon corstorphineiBroom & Haughton, 1917
  • Dicynodon curtusBroom, 1921
  • Dicynodon cyclopsHaughton, 1917
  • Dicynodon eurycepsBoonstra, 1938
  • Dicynodon graaffiBroom, 1940
  • Dicynodon greyiiOwen, 1860
  • Dicynodon helenaeBoonstra, 1938
  • Dicynodon kolbeiBroom, 1912
  • Dicynodon lutricepsBroom, 1912
  • Dicynodon maccabeiBroom, 1940
  • Dicynodon marlothiBroili & Schröder, 1917
  • Dicynodon megalopsOwen, 1876
  • Dicynodon moutonaeBroom, 1948
  • Dicynodon nesemanniBroom, 1940
  • Dicynodon parabrevicepsBoonstra, 1938
  • Dicynodon prognathusOwen, 1860
  • Dicynodon richardiBroom, 1940
  • Dicynodon robertsiBroom, 1948
  • Dicynodon schwarziBroom, 1919
  • Dicynodon truncatusBroom, 1899
  • Dicynodon vanderbyliBroom, 1928
  • Dicynodon wellwoodensisBroom, 1936
  • Oudenodon bolorhinusBroom, 1911
  • Oudenodon brevirostris(Owen, 1876)(originally Dicynodon brevirostris)
  • Oudenodon glaucops(Broom, 1948)(originally Oudenodon)
  • Oudenodon halli(Watson, 1914)(originally Dicyonodon halli)
  • Oudenodon latirostrisBroom, 1932
  • O. luangwensisBoonstra, 1938 [1]
  • Oudenodon mustoiHaughton, 1915
  • Oudenodon planus(Broom, 1913)(originally Dicynodon planus)
  • Oudenodon platyceps(Broom, 1913)(originally Dicynodon platyceps)<
  • Oudenodon platyfrons(Broom, 1932)(originally Dicynodon platyfrons)
  • Oudenodon robustus(Broom, 1932)(originally Dicynodon robustus)
  • Oudenodon wilmanae(Broom, 1928)(originally Dicynodon wilmanae)
Restoration of Oudenodon bainii Oudenodon.jpg
Restoration of Oudenodon bainii
Oudenodon latirostris skull Oudenodon latirostris.jpg
Oudenodon latirostris skull

Oudenodon is an extinct genus of dicynodont. It was common throughout southern Africa during the Late Permian. Several species of Oudenodon are known. [2] Both O. bainii, the type species, and O. grandis are known from South Africa. [3] [4] Specimens of O. luangwensis have been found from Zambia. [5] One species, O. sakamenensis, is the only Permian therapsid yet described from Madagascar. [6] It is the type genus of the family Oudenodontidae, which includes members such as Tropidostoma .

Contents

See also

Related Research Articles

<span class="mw-page-title-main">Dicynodontia</span> Extinct clade of therapsids

Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivores that typically bore a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typically toothless beak, unique amongst all synapsids. Dicynodonts first appeared in Southern Pangaea during the mid-Permian, ca. 270–260 million years ago, and became globally distributed and the dominant herbivorous animals in the Late Permian, ca. 260–252 Mya. They were devastated by the end-Permian Extinction that wiped out most other therapsids ca. 252 Mya. They rebounded during the Triassic but died out towards the end of that period. They were the most successful and diverse of the non-mammalian therapsids, with over 70 genera known, varying from rat-sized burrowers to elephant-sized browsers.

<i>Robertia</i> Extinct genus of dicynodonts

Robertia is an extinct genus of small herbivorous dicynodonts from the Middle to Late Permian of South Africa, between 260 and 265 million years ago. It is a monospecific genus, consisting of the type-species R. broomiana, which was classified by Lieuwe Dirk Boonstra in 1948 and named in honor of Robert Broom for his study of South African mammal-like reptiles.

<i>Cistecephalus</i> Extinct genus of dicynodonts

Cistecephalus is an extinct genus of dicynodont therapsid from the Late Permian of southern Africa. It was a small, specialised, burrowing dicynodont, possibly with habits similar to a modern mole. The head was flattened and wedge-shaped, the body long, and the forelimbs very strong, with similarities in structure to the forelimb of modern burrowing mammals.

<i>Diictodon</i> Extinct genus of dicynodonts

Diictodon is an extinct genus of pylaecephalid dicynodont that lived during the Late Permian period, approximately 255 million years ago. Fossils have been found in the Cistecephalus Assemblage Zone of the Madumabisa Mudstone of the Luangwa Basin in Zambia and the Tropidostoma Assemblage Zone of the Teekloof Formation, Tapinocephalus Assemblage Zone of the Abrahamskraal Formation, Dicynodon Assemblage Zone of the Balfour Formation, Cistecephalus Assemblage Zone of the Middleton or Balfour Formation of South Africa and the Guodikeng Formation of China. Roughly half of all Permian vertebrate specimens found in South Africa are those of Diictodon. This small herbivorous animal was one of the most successful synapsids in the Permian period.

<i>Dicynodon</i> Extinct genus of dicynodonts

Dicynodon is a genus of dicynodont therapsid that flourished during the Upper Permian period. Like all dicynodonts, it was an herbivorous animal. This synapsid was toothless, except for prominent tusks, hence the name. It probably cropped vegetation with a horny beak, much like a tortoise, while the tusks may have been used for digging up roots and tubers.

<i>Tropidostoma</i> Assemblage Zone

The Tropidostoma Assemblage Zone is a tetrapod assemblage zone or biozone which correlates to the lower Teekloof Formation, Adelaide Subgroup of the Beaufort Group, a fossiliferous and geologically important geological Group of the Karoo Supergroup in South Africa. The thickest outcrops, reaching approximately 240 metres (790 ft), occur from east of Sutherland through to Beaufort West and Victoria West, to areas south of Graaff-Reinet. Its northernmost exposures occur west/north-west of Colesberg. The Tropidostoma Assemblage Zone is the fourth biozone of the Beaufort Group.

<i>Eodicynodon</i> Extinct genus of dicynodonts

Eodicynodon is an extinct genus of dicynodont therapsids, a highly diverse group of herbivorous synapsids that were widespread during the middle-late Permian and early Triassic. As its name suggests, Eodicynodon is the oldest and most primitive dicynodont yet identified, ranging from the middle to late Permian and possessing a mix of ancestral anomodont/therapsid features and derived dicynodont synapomorphies.

<i>Endothiodon</i> Extinct genus of dicynodonts

Endothiodon is an extinct genus of medium to large dicynodont from the Late Permian. Like other dicynodonts, Endothiodon was an herbivore, but it typically lacked the two tusks that characterized most other dicynodonts and instead had long rows of teeth inset in the jaws that replaced in waves. The anterior portion of the upper and lower jaw are curved upward, creating a distinct beak that is thought to have allowed them to be specialized grazers.

<i>Myosaurus</i> Extinct genus of dicynodont from the lower Triassic

Myosaurus is a genus of dicynodont synapsids. Myosaurus was a small, herbivorous synapsid that existed around the early Triassic period. All of the fossils found of this species were found in Antarctica and South Africa. Compared to other fossils found from species that existed during this time, the Myosaurus is not common in the fossil record. This is due to a shortage of discovered fossils that possess characteristics unique to the Myosaurus. Notably, under 130 fossil fragments have been found that have been classified as Myosauridae, and almost all have been skulls. These skulls can be classified as Myosaurus because this species, unlike other dicynodonts, do not possess tusks or postfrontal teeth. The only species identified in the family Myosauridae is the Myosaurus gracilis, or M. gracilis. It should be recognized that the Myosaurus is almost always referred to as the M. gracilis in scientific research.

Digalodon is an extinct genus of kistecephalian dicynodont, known from the Karoo Basin of South Africa and the Upper Madumabisa Mudstone Formation of Zambia. Originally given a sparse description in 1948, for a time it was considered synonymous with other dicynodonts as a small juvenile individual of a larger genus, such as Aulacephalodon or Dicynodontoides; however it has since been recognized as a distinct species.

<i>Dicynodontoides</i> Extinct genus of dicynodonts

Dicynodontoides is a genus of small to medium-bodied, herbivorous, emydopoid dicynodonts from the Late Permian. The name Dicynodontoides references its “dicynodont-like” appearance due to the caniniform tusks featured by most members of this infraorder. Kingoria, a junior synonym, has been used more widely in the literature than the more obscure Dicynodontoides, which is similar-sounding to another distantly related genus of dicynodont, Dicynodon. Two species are recognized: D. recurvidens from South Africa, and D. nowacki from Tanzania.

<i>Odontocyclops</i> Extinct genus of dicynodonts

Odontocyclops is an extinct genus of Dicynodonts that lived in the Late Permian. Dicynodonts are believed to be the first major assemblage of terrestrial herbivores. Fossils of Odontocyclops have been found in the Karoo Basin of South Africa and the Luangwa Valley of Zambia. The phylogenetic classification of Odontocyclops has been long under debate, but most current research places them as their own genus of Dicynodonts and being very closely related to Rhachiocephalus and Oudenodon.

Prodicynodon is an extinct genus of dicynodont from the Late Permian of South Africa. Two species are known, the type species P. pearstonensis and P. beaufortensis, both known only from their respective holotypes.

<i>Tropidostoma</i> Extinct genus of dicynodonts

Tropidostoma is a medium-sized herbivorous oudenodontid dicynodont therapsid that lived during the Late Permian (Lopingian) period in South Africa. The first Tropidostoma fossil was described by Harry Govier Seeley in 1889. Later two subspecies were identified. Tropidostoma fossils are an index fossil in a biozone of the Karoo Basin known as the Tropidostoma Assemblage Zone. This biozone is characterized by the presence of this species in association with another dicynodont species, Endothiodon uniseries.

<i>Aulacephalodon</i> Extinct genus of dicynodonts

Aulacephalodon is an extinct genus of medium-sized dicynodonts, or non-mammalian synapsids, that lived during late Permian period. Individuals of Aulacephalodon are commonly found in the Lower Beaufort Group of the Karoo Supergroup of South Africa. Rising to dominance during the Late Permian, Aulacephalodon was among the largest terrestrial vertebrate herbivores until its extinction at the end of the Permian. Two species have been named, the type species, A. bainii, and a second species, A. peavoti. However, debate exists among paleontologists if A. peavoti is a true member of the genus Aulacephalodon. Aulacephalodon belongs to the family Geikiidae, a family of dicynodonts generally characterized by their short, broad skulls and large nasal bosses. Sexual dimorphism has been identified in A. bainii.

<span class="mw-page-title-main">Venyukovioidea</span> Extinct infraorder of therapsids

Venyukovioidea is an infraorder of anomodont therapsids related to dicynodonts from the Permian of Russia. They have also been known as 'Venjukovioidea', as well as by the similar names 'Venyukoviamorpha' or 'Venjukoviamorpha' in literature. This in part owes to a misspelling by Russian palaeontologist Ivan Efremov in 1940 when he mistakenly spelt Venyukovia, the namesake of the group, with a 'j' instead of a 'y', which permeated through subsequent therapsid literature before the mistake was caught and corrected. The order Ulemicia has also been coined for a similar taxonomic concept in Russian scientific literature, which notably excludes Suminia and Parasuminia.

<span class="mw-page-title-main">Abrahamskraal Formation</span> Geological formation of the Beaufort Group in South Africa

The Abrahamskraal Formation is a geological formation and is found in numerous localities in the Northern Cape, Western Cape, and the Eastern Cape of South Africa. It is the lowermost formation of the Adelaide Subgroup of the Beaufort Group, a major geological group that forms part of the greater Karoo Supergroup. It represents the first fully terrestrial geological deposits of the Karoo Basin. Outcrops of the Abrahamskraal Formation are found from the small town Middelpos in its westernmost localities, then around Sutherland, the Moordenaarskaroo north of Laingsburg, Williston, Fraserburg, Leeu-Gamka, Loxton, and Victoria West in the Western Cape and Northern Cape. In the Eastern Cape outcrops are known from Rietbron, north of Klipplaat and Grahamstown, and also southwest of East London.

<i>Gordonia</i> (synapsid) Extinct genus of dicynodonts

Gordonia is an extinct genus of dicynodont therapsid from the Late Permian of Scotland. Fossils have been found from the Elgin sandstone of Cutties Hillock Sandstone in Elgin, Moray. These are among the many amniote fossils referred to as the Elgin Reptiles. Gordonia was named in 1893 with four species: G. traquairi, G. duffiana, G. huxleyana, and G. juddiana. Currently, the only recognized species is the type G. traquairi. All other species are considered synonyms of the type.

<i>Turfanodon</i> Extinct genus of dicynodonts

Turfanodon is an extinct genus of dicynodont therapsid from the Late Permian Sunan, Guodikeng, and Naobaogou Formations of China. The holotype of T. bogdaensis was discovered between 1963-1964 and was originally named in 1973 by A. Sun with the type species Turfanodon bogdaensis, Turfanodon was reclassified as a junior synonym of the related Dicynodon in 1988 by G. M. King. T. bogdaensis remained a species of Dicynodon for over two decades before the genus was reinstated in 2011 in a revision of the taxonomy of Dicynodon by palaeontologist Christian Kammerer. A second species from Inner Mongolia, T. jiufengensis, was named in 2021 by palaeontologist Jun Liu from a nearly complete skeleton and other referred bones. Turfanodon was a relatively large dicynodont, and similar in appearance to the related Daptocephalus from South Africa.

<i>Bulbasaurus</i> Extinct genus of dicynodonts

Bulbasaurus is an extinct genus of dicynodont that is known from the Lopingian epoch of the Late Permian period of what is now South Africa, containing the type and only species B. phylloxyron. It was formerly considered as belonging to Tropidostoma; however, due to numerous differences from Tropidostoma in terms of skull morphology and size, it has been reclassified the earliest known member of the family Geikiidae, and the only member of the group known from the Tropidostoma Assemblage Zone. Within the Geikiidae, it has been placed close to Aulacephalodon, although a more basal position is not implausible.

References

  1. Boonstra, L. D. (1938). A report of some Karoo reptiles from the Luangwa Valley, Northern Rhodesia. Quaternary Journal of the Geological Society of London94:371-384.
  2. King, G. (1988). Anomodontia. Encyclopedia of Paleoherpetology17C:1-174.
  3. Owen, R. (1860). On some reptilian fossils from South Africa. Quaternary Journal of the Geological Assotiation of South Africa67:1-110.
  4. Haughton, S. H. (1917). Investigations in South African fossil reptiles and Amphibia. Part 10. Descriptive catalogue of the Dicynodontia. Annals of the South African Museum12:127-174.
  5. Keyser, A. W. (1975). A re-evaluation of the cranial morphology and systematics of some tuskless Anomodontia. Memoir of the Geological Society of South Africa67:1-110.
  6. Mazin, J. M. and King, G. M. (1991). The first dicynodont from the Late Permian of Malagasy. Palaeontology34:837–842.