An anapsid is an amniote whose skull lacks one or more skull openings near the temples. Traditionally, the Anapsida are the most primitive subclass of amniotes, the ancestral stock from which Synapsida and Diapsida evolved, making anapsids paraphyletic. It is however doubtful that all anapsids lack temporal fenestra as a primitive trait, and that all the groups traditionally seen as anapsids truly lacked fenestra.
Anomodontia is an extinct group of non-mammalian therapsids from the Permian and Triassic periods. By far the most speciose group are the dicynodonts, a clade of beaked, tusked herbivores. Anomodonts were very diverse during the Middle Permian, including primitive forms like Anomocephalus and Patranomodon and groups like Venyukovioidea and Dromasauria. Dicynodonts became the most successful and abundant of all herbivores in the Late Permian, filling ecological niches ranging from large browsers down to small burrowers. Few dicynodont families survived the Permian–Triassic extinction event, but one lineage (Kannemeyeriiformes) evolved into large, stocky forms that became dominant terrestrial herbivores right until the Late Triassic, when changing conditions caused them to decline, finally going extinct during the Triassic–Jurassic extinction event.
Parareptilia ("near-reptiles") is a subclass or clade of basal sauropsids/reptiles, typically considered the sister taxon to Eureptilia. Parareptiles first arose near the end of the Carboniferous period and achieved their highest diversity during the Permian period. Several ecological innovations were first accomplished by parareptiles among reptiles. These include the first reptiles to return to marine ecosystems (mesosaurs), the first bipedal reptiles, the first reptiles with advanced hearing systems, and the first large herbivorous reptiles. The only parareptiles to survive into the Triassic period were the procolophonoids, a group of small generalists, omnivores, and herbivores. The largest family of procolophonoids, the procolophonids, rediversified in the Triassic, but subsequently declined and became extinct by the end of the period.
Procolophon is a genus of lizard-like procolophonid parareptiles that first appeared in the Early Triassic (Induan) of South Africa, Brazil, and Antarctica. It persisted through the Permian–Triassic extinction event, but went extinct in the beginning of the Early Middle Triassic. The type species is P. trigoniceps.
Sclerosaurus is an extinct genus of procolophonid parareptile known from the Early to Middle Triassic of Germany and Switzerland. It contains a single species, Sclerosaurus armatus. It was fairly small, about 30 cm long, distinguished from other known parareptiles by the possession of long, backwardly projecting spikes, rear lower jaw teeth with slightly imbricating crowns, and a narrow band of back armor comprising two or three rows of sculptured osteoderms on either side of the midline.
Eunotosaurus is an extinct genus of amniote, possibly a close relative of turtles. Eunotosaurus lived in the late Middle Permian and fossils can be found in the Karoo Supergroup of South Africa. Eunotosaurus resided in the swamps of southern Africa. Its ribs were wide and flat, forming broad plates similar to a primitive turtle shell, and the vertebrae were nearly identical to those of some turtles. Accordingly, it is often considered as a possible transitional fossil between turtles and their prehistoric ancestors. However, it is possible that these turtle-like features evolved independently of the same features in turtles, since other anatomical studies and phylogenetic analyses suggest that Eunotosaurus may instead have been a parareptile, an early-diverging neodiapsid unrelated to turtles, or a synapsid.
Sauropareion is an extinct genus of basal procolophonid parareptile from earliest Triassic deposits of Eastern Cape Province, South Africa. It is known from the holotype SAM PK-11192, skull and partial postcranium. It was collected by the late L. D. Boonstra in 1935 from Barendskraal in the Middelburg District and referred to the Lystrosaurus Assemblage Zone of the Beaufort Group. It was first named by Sean P. Modesto, Hans-Dieter Sues and Ross J. Damiani in 2001 and the type species is Sauropareion anoplus. The generic name means "lizard", sauros, and "cheek", pareion from Greek in reference to the lizard-like appearance of the temporal region. The specific name comes from the Greek word anoplos, meaning "without arms or armour".
Pintosaurus is an extinct genus of basal procolophonid parareptile from Late Triassic deposits of northeastern Uruguay. It is known from the holotype FC-DPV 1181, a partial skull. It was collected from the Buena Vista Formation of the Paraná Basin, in Colonia Orozco, Cerro Largo Department. It was first named by Graciela Piñeiro, Alejandra Rojas and Martín Ubilla in 2004 and the type species is Pintosaurus magnidentis. The generic name honours Dr. Iraja Damiani Pinto. The specific name means "with a large tooth" in Latin, a reference to the large palatal tooth pair.
Theledectes is an extinct genus of theledectine procolophonid parareptile from middle Triassic deposits of Free State Province, South Africa.The type species, Theledectes perforatus, is based on the holotype BP/1/4585, a flattened skull. This skull was collected by the South African palaeontologist, James W. Kitching from Hugoskop in the Rouxville District and referred to subzone B of the Cynognathus Assemblage Zone of the Burgersdorp Formation, Beaufort Group. The genus was first named by Sean P. Modesto and Ross J. Damiani in 2003. However, the species was initially assigned to the genus Thelegnathus by C.E. Gow in 1977, as the species Thelegnathus perforatus.
Phaanthosaurus is an extinct genus of basal procolophonid parareptile from early Triassic deposits of Nizhnii Novgorod, Russian Federation. It is known from the holotype PIN 1025/1, a mandible. It was collected from Vetluga River, Spasskoe village and referred to the Vokhmian terrestrial horizon of the Vokhma Formation. It was first named by P. K. Chudinov and B. P. Vjushkov in 1956 and the type species is Phaanthosaurus ignatjevi.
Ankyramorpha is an extinct clade of procolophonomorph parareptiles which lived between the early Cisuralian epoch and the latest Triassic period of Africa, Antarctica, Asia, Australia, Europe, North America and South America.
Lanthanosuchoidea is an extinct superfamily of ankyramorph parareptiles from the middle Pennsylvanian to the middle Guadalupian epoch of Europe, North America and Asia. It was named by the Russian paleontologist Ivachnenko in 1980, and it contains two families Acleistorhinidae and Lanthanosuchidae.
Eumetabolodon is an extinct genus of procolophonine procolophonid parareptile from early and middle Triassic deposits of Nei Mongol, northern China. Two species of Eumetabolodon were named by J. L. Li in 1983 and the type species is Eumetabolodon bathycephalus.
Anomoiodon is an extinct genus of procolophonine procolophonid parareptile from early Triassic deposits of Thuringia, Germany. It is known only from the holotype MB.R.3539B and paratype MB.R.3539A, two articulated, three-dimensionally preserved partial skeletons on one block which represent two individuals. The holotype includes nearly complete skull and lower jaw. The block was collected from the lowest layer of the Chirotherium Sandstone Member of the Solling Formation, dating to the early Olenekian faunal stage of the Early Triassic, about 249-247 million years ago. It was first named by Friedrich von Huene in 1939 and the type species is Anomoiodon liliensterni. Laura K. Säilä, who redescribed Anomoiodon in 2008, found it to be a leptopleuronine using a phylogenetic analysis. The most recent analysis, performed by Ruta et al. (2011) found it to be a procolophonine instead. However, both analyses found that it is most closely related to the Russian procolophonid Kapes.
Procolophoninae is an extinct subfamily of procolophonid parareptiles from the late Early Triassic to the early Middle Triassic of Africa, Antarctica, Asia, Europe and South America. Currently, the oldest-known procolophonine is Procolophon from the earliest Olenekian stage.
Leptopleuroninae is an extinct subfamily of procolophonid reptiles. The oldest member of Leptopleuroninae is Phonodus dutoitorum from the Induan age of the Early Triassic. It is the only procolophonid group that survived into the Late Triassic.
Pentaedrusaurus is an extinct genus of procolophonid parareptile from the Early Triassic of China. It is one of the most basal members of the procolophonid subfamily Leptopleuroninae. The only known species of Pentaedrusaurus, P. ordosianus, was named in 1989 from the Heshanggou Formation.
Scoloparia is an extinct genus of procolophonid parareptile from the Triassic of Canada. Fossils have been found in the Early Triassic to Norian-age Wolfville Formation in Nova Scotia, Canada. Like many Triassic procolophonids, Scoloparia has expanded molar-like teeth that indicate that the animal was likely herbivorous.
Kapes is an extinct genus of procolophonid parareptile from the Lower and Middle Triassic of the United Kingdom and Russia. It is a member of the subfamily Procolophoninae. The type species K. amaenus was named in 1975 from the banks of the Vychegda River in the Komi Republic of Russia. In 1983, a new species was brought into the genus, K. majmesculae. K. majmesculae was first named in 1968 as a member of the genus Tichvinskia. A third Russian species, K. serotinus, was named in 1991. In 2002, Kapes bentoni was named from the Middle Triassic Otter Sandstone Formation of Devon, England, extending the geographic range of Kapes. In the same paper, K. serotinus was synonymized with K. majmesculae and another Russian species was assigned to Kapes called K. komiensis. K. komiensis was first named in 1975 as a member of the genus Macrophon.
Barasaurus is an extinct genus of owenettid procolophonoid parareptile known from the Late Permian and Early Triassic of Madagascar. It contains a single species, Barasaurus besairiei.
