Lungfish are freshwater vertebrates belonging to the class Dipnoi. Lungfish are best known for retaining ancestral characteristics within the Osteichthyes, including the ability to breathe air, and ancestral structures within Sarcopterygii, including the presence of lobed fins with a well-developed internal skeleton. Lungfish represent the closest living relatives of the tetrapods. The mouths of lungfish typically bear tooth plates, which are used to crush hard shelled organisms.
Ceratodontidae is an extinct family of lungfish with fossils known worldwide from the earliest Triassic to the Eocene.
Protopterus is the genus of four species of lungfish found in Africa. Protopterus is considered the sole genus in the family Protopteridae, which is grouped with Lepidosiren in the order Lepidosireniformes.
"Labyrinthodontia" is an informal grouping of extinct predatory amphibians which were major components of ecosystems in the late Paleozoic and early Mesozoic eras. Traditionally considered a subclass of the class Amphibia, modern classification systems recognize that labyrinthodonts are not a formal natural group (clade) exclusive of other tetrapods. Instead, they consistute an evolutionary grade, ancestral to living tetrapods such as lissamphibians and amniotes. "Labyrinthodont"-grade vertebrates evolved from lobe-finned fishes in the Devonian, though a formal boundary between fish and amphibian is difficult to define at this point in time.
Microsauria is an extinct, possibly polyphyletic order of tetrapods from the late Carboniferous and early Permian periods. It is the most diverse and species-rich group of lepospondyls. Recently, Microsauria has been considered paraphyletic, as several other non-microsaur lepospondyl groups such as Lysorophia seem to be nested in it. Microsauria is now commonly used as a collective term for the grade of lepospondyls that were originally classified as members of Microsauria.
The Tapinocephalus Assemblage Zone is a tetrapod assemblage zone or biozone which correlates to the middle Abrahamskraal 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 2,000 metres (6,600 ft), occur from Merweville and Leeu-Gamka in its southernmost exposures, from Sutherland through to Beaufort West where outcrops start to only be found in the south-east, north of Oudshoorn and Willowmore, reaching up to areas south of Graaff-Reinet. Its northernmost exposures occur around the towns Fraserburg and Victoria West. The Tapinocephalus Assemblage Zone is the second biozone of the Beaufort Group.
The Daptocephalus Assemblage Zone is a tetrapod assemblage zone or biozone found in the Adelaide Subgroup of the Beaufort Group, a majorly fossiliferous and geologically important Group of the Karoo Supergroup in South Africa. This biozone has outcrops located in the upper Teekloof Formation west of 24°E, the majority of the Balfour Formation east of 24°E, and the Normandien Formation in the north. It has numerous localities which are spread out from Colesberg in the Northern Cape, Graaff-Reniet to Mthatha in the Eastern Cape, and from Bloemfontein to Harrismith in the Free State. The Daptocephalus Assemblage Zone is one of eight biozones found in the Beaufort Group and is considered Late Permian (Lopingian) in age. Its contact with the overlying Lystrosaurus Assemblage Zone marks the Permian-Triassic boundary.
The Pristerognathus Assemblage Zone is a tetrapod assemblage zone or biozone which correlates to the upper Abrahamskraal Formation and lowermost 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 not more than 300 metres (980 ft), occur just east of Sutherland through to Beaufort West in the south and Victoria West in the north. Exposures are also found west of Colesberg and south of Graaff-Reinet. The Pristerognathus Assemblage Zone is the third biozone of the Beaufort Group.
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.
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.
Ferganoceratodus is a genus of prehistoric lungfish known from the Mesozoic of Asia and Africa. Based on morphological evidence, it has either been recovered as a basal member of the Ceratodontiformes or to be the sister group of the Neoceratodontidae.
Gnathorhiza is an extinct genus of prehistoric lobe-finned fish (lungfish) which lived from the Carboniferous period to the Early Triassic epoch. It is the only known lungfish genus to have crossed the Permo-Triassic boundary. Several species have been described, ranging in size from 5 to 50 centimeters.
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.
Pelanomodon is an extinct genus of dicynodont therapsids that lived in the Late Permian period. Fossil evidence of this genus is principally found in the Karoo Basin of South Africa, in the Dicynodon Assemblage Zone. Lack of fossil record after the Late Permian epoch suggests that Pelanomodon fell victim to the Permian-Triassic extinction event.
Ptychoceratodus is an extinct genus of lungfish living from Early Triassic to Middle Jurassic. It was established by Otto Jaekel for one species, transferred from Ceratodus genus. Type species is P. serratus from the Middle Triassic of Switzerland and Germany. Ptychoceratodus had two pairs of massive dental plates, bearing 4-6 acute ridges. Its skull roof was composed from massive, plate-like bones. In the central part of skull roof was localized an unossified fenestra. Most of the Ptychoceratodus findings are isolated dental plates, some associated with jaws. Other parts of skull or postcranial skeleton are relatively rarely found as fossils. The anatomy of skull is the best recognized in P. serratus, whereas less complete cranial material is available also for P. concinuus, P. phillipsi, and P. rectangulus. Although Ptychoceratodus is known exclusively from the Triassic and Jurassic, there were also Cretaceous specimens referred to this genus. However, they are more often regarded as representants of Metaceratodus. Ptychoceratodus is the only member of the family Ptychoceratodontidae. The first named species is P. phillipsi by Louis Agassiz in 1837 as a species of Ceratodus and later moved to Ptychoceratodus genus. Occurrences of Ptychoceratodus come mainly from Europe. However, occurrences from other continents suggest it was dispersed globally during the Triassic. After 2010, the new fossil material behind the Europe was reported from South America, India, and Greenland
Kombuisia is a genus of dicynodont from Early to Middle Triassic of South Africa and Antarctica. Two species were described for the genus: Kombuisia frerensis (type) and Kombuisia antarctica.
Syops is an extinct genus of dicynodont therapsid. The type species S. vanhoepeni was first named in 1938 as Dicynodon vanhoepeni. Fossils of the genus have been found in the Cistecephalus Assemblage Zone in the Usili Formation of the Ruhuhu Basin, Tanzania and the Upper Madumabisa Mudstone Formation of the Luangwa Basin, Zambia. Its phylogenetic placement is somewhat uncertain, with multiple different studies finding it as either a basal geikiid, rhachiocephalid a dicynodontoid more derived than the most basal genera but less derived than Lystrosauridae, or a lystrosaurid.
The Red Beds of Texas and Oklahoma are a group of Early Permian-age geologic strata in the southwestern United States cropping out in north-central Texas and south-central Oklahoma. They comprise several stratigraphic groups, including the Clear Fork Group, the Wichita Group, and the Pease River Group. The Red Beds were first explored by American paleontologist Edward Drinker Cope starting in 1877. Fossil remains of many Permian tetrapods have been found in the Red Beds, including those of Dimetrodon, Edaphosaurus, Seymouria, Platyhystrix, and Eryops. A recurring feature in many of these animals is the sail structure on their backs.
Huskerpeton is an extinct genus of recumbirostran from the Early Permian period. They belong to the order Microsauria, which was established in 1863 by Dawson, and was quickly expanded to include many different small taxa. They lived in what is now Nebraska and Kansas. The holotype of Huskerpeton was uncovered at the Eskridge formation in Nebraska, which is part of how it got its name.
Ceratodontiformes is the only extant order of lungfish, containing the families Neoceratodontidae, Lepidosirenidae, and Protopteridae as well as many other extinct groups. Members of this group are the only lungfish known to have survived the Permian-Triassic extinction event. Although lungfish originated in marine environments, the Ceratodontiformes have been an exclusively freshwater group since the Carboniferous. This order was formerly considered the suborder Ceratodontoidei.
