Dicynodontia is a taxon of anomodont therapsids with beginnings in the mid-Permian, which were dominant in the Late Permian, survived the Permian Extinction that wiped out most other therapsids and continued on throughout the Triassic before dying out at the end of the period. Dicynodonts were herbivorous animals with two tusks, hence their name, which means 'two dog tooth'. They are also the most successful and diverse of the non-mammalian therapsids, with over 70 genera known, varying from rat- to elephant-sized.
Anomodontia is an extinct group of non-mammalian therapsids containing many species from the Permian and Triassic periods, most of which were toothless, possibly endothermic herbivores. Anomodonts were very diverse during the Middle Permian, including primitive forms like Anomocephalus and Patranomodon and groups like Venyukovioidea, Dromasauria, and Dicynodontia. Of these, only the dicynodonts survived beyond the Middle Permian. Dicynodonts became the most successful and abundant of all herbivores in the Late Permian and Triassic, filling ecological niches ranging from large browsers down to small burrowers. Few dicynodont families survived the Permian–Triassic extinction event, but one lineage evolved into large, stocky forms that remained the dominant terrestrial herbivores right until the Late Triassic, when changing conditions caused them to decline.
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.
Dicynodon is a genus of dicynodont therapsid that flourished during the Upper Permian period. Like all dicynodonts, it was herbivorous. This animal 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.
Daptocephalus is an extinct genus of non-mammalian synapsid anomodont dicynodont, it which was found in Late Permian strata, in a biozone known precisely for the presence of fossils of this dicynodont, the Daptocephalus Zone, in the Karoo Basin in South Africa. An additional species, D. huenei, is known from the Usili Formation in Tanzania and was formerly assigned to the genus Dicynodon before a study in 2019 recognised that the type specimen belonged to Daptocephalus.
Aulacephalodon is an extinct genus of medium-sized dicynodonts, or non-mammalian synapsids, that lived during Permian period, about 299-252 million years ago. Individuals of Aulacephalodon are commonly found in the Lower Beaufort Group of the Karoo Supergroup of South Africa and Zambia. Rising to dominance during the Late Permian, Aulacephalodon were the dominant terrestrial vertebrate herbivores until they became extinct during the Triassic. No living relatives of Aulacephalodon exist today. 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. Therefore, a majority of the information known about Aulacephalodon is in reference to discoveries about A. bainii.
Cryptodontia is a group of dicynodont therapsids that includes the families Geikiidae, Oudenodontidae, and Rhachiocephalidae. It was first named in 1860 by English paleontologist Richard Owen. Owen intended Cryptodontia to be a family, and the name was later changed to "Cryptodontidae" to reflect this ranking. The name Cryptodontia was restored in 2009 when it was redefined as a larger clade containing several families of dicynodonts.
Keyseria is an extinct genus of dicynodont therapsid. The type species K. benjamini was first named in 1948 as Dicynodon benjamini.
Basilodon is an extinct genus of dicynodont therapsid. The type species B. woodwardi was originally named in 1921 as Dicynodon woodwardi. Fossils have been found in the Cistecephalus Assemblage Zone and Dicynodon Assemblage Zone of the Balfour Formation of the Beaufort Group in South Africa.
Therochelonia is a group of dicynodont therapsids. The group was named by British paleontologist Harry Seeley in 1894 and fell into disuse in the following century. Therochelonia was redefined as a node-based clade in 2009. It is defined as the last common ancestor of Cistecephalus microrhinus and Dicynodon lacerticeps, and all of its descendants. Below is a simplified cladogram from Kammerer et al. (2011) showing the phylogenetic placement of Therochelonia:
Sintocephalus is an extinct genus of dicynodont therapsid from the Late Permian of South Africa. Fossils are known from the Cistecephalus Assemblage Zone of the Beaufort Group. The type species of Sintocephalus, S. alticeps, was first named in 1913 as a species of Dicynodon. The genus was erected in 1934, but in subsequent years its species were often regarded as members of other dicynodont genera.
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 Quarry in Elgin, Moray. These are among the many reptile 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.
Bidentalia is a group of dicynodont therapsids. Bidentalia was one of the first names used to describe dicynodonts; the group was established in 1876, while the name "bidentals" dates back as far as 1845. With the increasing prominence of phylogenetics, the group was redefined as a clade in 2009. Bidentalia is now considered a stem-based taxon that includes all taxa more closely related to Aulacephalodon bainii and Dicynodon lacerticeps than Emydops arctatus.
Daqingshanodon is an extinct genus of dicynodont therapsid from the Late Permian of Inner Mongolia, China. The type species D. limbus was described in 1989 from a single skull found in the Naobaogou Formation. Daqingshanodon belongs to a group of dicynodonts called cryptodonts. It is the smallest known cryptodont, and the only one known from China. Like other cryptodonts, it has a pair of rounded nasal bosses above its nostrils and a ridge of bone on the upper jaw called the postcaniniform process. Daqingshanodon has a pair of elongated, recurved tusks extending from its beak-like snout. It is distinguished from other dicynodonts by the presence of a distinct ridge running along the side of the skull from below the eye socket to the area around the tusks. The skull of Daqingshanodon is less than 10 centimetres (3.9 in) long, yet this specimen is thought to have been an adult on the basis of its well-developed nasal bosses.
Emydopoidea is a group of Late Permian dicynodont therapsids. It includes the small-bodied Emydops, Myosaurus, and kingoriids, and the burrowing cistecephalids. Below is a cladogram from Kammerer et al. (2011) showing the phylogenetic relationships of emydopoids:
Kistecephalia is a clade of dicynodont therapsids. The group was first named in 1894, and was reinstated as a clade in 2009. Kistecephalia is a stem-based taxon defined as all taxa more closely related to Cistecephalus microrhinus than Emydops arctatus. It includes the families Myosauridae, Kingoriidae, and Cistecephalidae and is part of the larger group Emydopoidea. Kistecephalians were small in comparison to other dicynodonts. One group of kistecephalians, the cistecephalids, are thought to have been burrowers. Below is a cladogram from Kammerer et al. (2011) showing the phylogenetic relationships of kistecephalians:
Jimusaria is an extinct genus of dicynodont therapsid from the Late Permian (Changhsingian) Guodikeng Formation of China. The type species J. sinkianensis was originally named as a species of Dicynodon, the first from Asia, but was given its own genus in 1963 before being sunk back into Dicynodon in 1988. The genus was resurrected in 2011 by palaeontologist Christian Kammerer in a taxonomic revision of the genus Dicynodon. Jimusaria was a mid-sized dicynodont, and was similar in appearance to the South African Dicynodon, but differed from it in features such as its narrower snout.
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.
The Usili Formation is a Late Permian geologic formation in Tanzania. It preserves fossils of many terrestrial vertebrates from the Permian, including temnospondyls, pareiasaurs, therapsids and the archosauromorph Aenigmastropheus.
Taoheodon is an extinct genus of dicynodont therapsid from the Sunjiagou Formation in the Shanxi province of China, dated to the Wuchiapingian age of the Late Permian. Its type and only known species is T. baizhijuni. Taoheodon was a close relative of the well known Dicynodon, and may represent a biogeographical link between the South African Dicynodon and similar dicynodonts found in Laos.
