Lystrosaurus is an extinct genus of herbivorous dicynodont therapsids from the late Permian and Early Triassic epochs. It lived in what is now Antarctica, India, China, Mongolia, European Russia and South Africa. Four to six species are currently recognized, although from the 1930s to 1970s the number of species was thought to be much higher. They ranged in size from that of a small dog to 8 feet (2.5 meters) long.
Ericiolacerta is an extinct genus of small therocephalian therapsids from the early Triassic of South Africa and Antarctica. Ericiolacerta, meaning "hedgehog lizard", was named by D.M.S. Watson in 1931. The species E. parva is known from the holotype specimen which consists of a nearly complete skeleton found in the Lystrosaurus Assemblage Zone within the Katberg Formation of the Beaufort Group in South Africa, and from a partial jaw found in the Lower Triassic Fremouw Formation in Antarctica. Ericiolacerta was around 20 centimetres (7.9 in) in length, with long limbs and relatively small teeth. It probably ate insects and other small invertebrates. The therocephalians – therapsids with mammal-like heads – were abundant in Permian times, but only a few made it into the Triassic. Ericiolacerta was one of those. It is possible that they gave rise to the cynodonts, the only therapsid group to survive into post-Triassic times. Cynodonts gave rise to mammals.
Therocephalia is an extinct clade of eutheriodont therapsids from the Permian and Triassic periods. The therocephalians ("beast-heads") are named after their large skulls, which, along with the structure of their teeth, suggest that they were carnivores. Like other non-mammalian synapsids, therocephalians were once described as "mammal-like reptiles". Therocephalia is the group most closely related to the cynodonts, which gave rise to the mammals, and this relationship takes evidence in a variety of skeletal features. Indeed, it had been proposed that cynodonts may have evolved from therocephalians and so that therocephalians as recognised are paraphyletic in relation to cynodonts.
The theriodonts are a major group of therapsids which appeared during the Middle Permian and which includes the gorgonopsians and the eutheriodonts, itself including the therocephalians and the cynodonts.
Moschorhinus is an extinct genus of therocephalian synapsid in the family Akidnognathidae with only one species: M. kitchingi, which has been found in the Late Permian to Early Triassic of the South African Karoo Supergroup. It was a large carnivorous therapsid, reaching 1.1–1.5 metres (3.6–4.9 ft) in total body length with the largest skull comparable to that of a lion in size, and had a broad, blunt snout which bore long, straight canines.
Regisaurus is an extinct genus of small carnivorous therocephalian. It is known from a single described species, the type species Regisaurus jacobi, from the Early Triassic Lystrosaurus Assemblage Zone of South Africa, although at least one undescribed species is also known.
Tetracynodon is an extinct genus of therocephalian. Fossils of Tetracynodon have been found in the Karoo Basin of South Africa. Two species are known: the type species T. tenuis from the Late Permian and the species T. darti from the Early Triassic. Both species were small-bodied and probably fed on insects and small vertebrates. Although Tetracynodon is more closely related to mammals than to reptiles, its braincase is very primitive and more resembles that of modern amphibians and reptiles than of mammals.
Pedaeosaurus is an extinct genus of therocephalian therapsids. Fossils have been found from the Fremouw Formation in the southern Transantarctic Mountains of Antarctica. Pedaeosaurus has traditionally been classified as a scaloposaurid and more recently as an ericiolacertid closely related to Ericiolacerta.
Rhigosaurus glacialis is a species of therocephalian therapsid. Its fossilized remains have been found in the Fremouw Formation of Antarctica and Australia. Part of a juvenile skull was found near Mount Kenyon, Antarctica. The holotype of the partial skull shows evidence of promiment upper and lower canine teeth.
Akidnognathidae is an extinct family of therocephalian therapsids from the Late Permian and Early Triassic of South Africa, Russia and China. The family includes many large-bodied therocephalians that were probably carnivorous, including Moschorhinus and Olivierosuchus. One akidnognathid, Euchambersia, may even have been venomous. Akidnognathids have robust skulls with a pair of large caniniform teeth in their upper jaws. The family is morphologically intermediate between the more basal therocephalian group Scylacosauridae and the more derived group Baurioidea.
Olivierosuchus is an extinct genus of therocephalian therapsids. It is a member of the family Akidnognathidae. Fossils of Olivierosuchus have been found from the Early Triassic Lystrosaurus Assemblage Zone in South Africa. Unlike other akidnognathids such as Moschorhinus, it has a narrow snout and fewer postcanine teeth. As a distinguishing feature, Olivierosuchus also has a sharp ridge near the choana, an opening in the skull palate. Bumps and projections cover the pterygoid, a bone that forms part of the palate.
Silphedosuchus is an extinct genus of therocephalian therapsids from the Early Triassic of Russia. It is a member of the family Ericiolacertidae, along with the genus Ericiolacerta from South Africa and Antarctica. The type species Silphedosuchus orenburgensis was described in 1977 on the basis of a single holotype skull from Orenburg Oblast.
Blattoidealestes is an extinct genus of therocephalian therapsid from the Middle Permian of South Africa. The type species Blattoidealestes gracilis was named by South African paleontologist Lieuwe Dirk Boonstra from the Tapinocephalus Assemblage Zone in 1954. Dating back to the Middle Permian, Blattoidealestes is one of the oldest therocephalians. It is similar in appearance to the small therocephalian Perplexisaurus from Russia, and may be closely related.
Homodontosaurus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. The type species Homodontosaurus kitchingi was named by South African paleontologist Robert Broom in 1949. Broom based his description on a small skull found in the Cistecephalus Assemblage Zone near Graaff-Reinet. The skull is very small, at about 55 millimetres (2.2 in) long and 20 millimetres (0.79 in) wide. Homodontosaurus has large eye sockets and an elongated snout. The lower jaw is long, thin, and curved. Numerous small teeth line the upper jaw and are long, pointed, and round in cross-section.
Scalopodon is an extinct genus of therocephalian therapsids from the Late Permian of Russia. The type species Scalopodon tenuisfrons was named in 1999 from the Kotelnichsky District of Kirov Oblast. Scalopodon is known from a single fragmentary holotype specimen including the back of the skull, the left side of the lower jaw and isolated postorbital and prefrontal bones. The skull was found in the Deltavjatia Assemblage Zone, which dates back to the early Wuchiapingian about 260 million years ago. Distinguishing features of Scalopodon include narrow frontal bones and a distinctive sagittal crest along the parietal region at the back of the skull. Scalopodon was originally classified in the family Scaloposauridae, and was the first scaloposaurid found in Russia. More recent studies of therocephalians have found scaloposaurids like Scalopodon to be juvenile forms of larger therocephalians and do not consider Scaloposauridae to be a valid group. Scalopodon and most other scaloposaurids are now classified as basal members of Baurioidea.
Pelictosuchus is an extinct genus of therocephalian therapsids from the Late Permian of South Africa. It is classified in the family Akidnognathidae. The type species Pelictosuchus paucidens was named by South African paleontologist Robert Broom in 1940 from the Dicynodon Assemblage Zone.
Diademodontidae is an extinct family of Triassic gomphodonts. The best-known genus is Diademodon from South Africa. Titanogomphodon from Namibia may also be a member of Diademodontidae. The Chinese genera Hazhenia and Ordosiodon have also been included in the family, but were more recently identified as baurioid therocephalians. Remains of a diademodontid were reported in the Early-Middle Triassic Fremouw Formation in Antarctica, but that specimen was later referred to the trirachodontid Impidens.
Ordosiodon is an extinct genus of therocephalian therapsids from the Early Triassic of China. It includes two species, O. lincheyuensis and O. youngi.
Hazhenia is an extinct genus of therocephalian therapsids from the Early Triassic of China, of which Hazhenia concava is the only species. Hazhenia was named in 1981 from the Heshanggou Formation in the Ordos Desert of Inner Mongolia. It lived during the Olenekian Age of the Early Triassic, about 247 million years ago. Hazhenia belongs to a group of therocephalians called Baurioidea and possesses many mammal-like features such as cusped teeth and a secondary palate, both of which evolved independently in baurioids. Within Baurioidea it is most closely related to the genus Ordosiodon, which is also known from Inner Mongolia but comes from the slightly younger Ermaying Formation. Both genera were once placed in the family Ordosiidae, but as the name is preoccupied by a family of Cambrian trilobites, it is no longer valid.
Ericiolacertidae is a family of therocephalian therapsids. The family living in the earliest Triassic after the Permian-Triassic extinction event. Genera are: Ericiolacerta found in the Fremouw Formation of Antarctica and the Normandien Formation of South Africa, Pedaeosaurus found in the Fremouw Formation of Antarctica and Silphedosuchus, from the Petropavlovka Formation of Russia, east of the Urals. The family is composed of carnivores.
