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Pareiasauria

Pareiasauria Temporal range: Middle Permian - Late Permian, 265–252 Ma PreꞒ Ꞓ O S D C P T J K Pg N
Skeleton of Scutosaurus karpinskii in the American Museum of Natural History
Scientific classification
Domain:	Eukaryota
Kingdom:	Animalia
Phylum:	Chordata
Class:	Reptilia
Clade:	†Parareptilia
Order:	†Procolophonomorpha
Node:	†Ankyramorpha
Suborder:	†Procolophonia
Clade:	†Pareiasauromorpha
Superfamily:	†Pareiasauroidea
Clade:	†Pareiasauria Seeley, 1888
Genera
†Bradysaurus †Bunostegos †Deltavjatia †Embrithosaurus †Parasaurus †Senectosaurus †Velosauria †Pumiliopareiasauria †Anthodon †Nanopareia †Provelosaurus †Pumiliopareia †Therischia †Arganaceras †Pareiasaurus †Sanchuansaurus †Scutosaurus †Shihtienfenia †Elgininiinae †Elginia †Obirkovia

Pareiasaurs (meaning "cheek lizards") are an extinct clade of large, herbivorous parareptiles. Members of the group were armoured with osteoderms which covered large areas of the body. They first appeared in southern Pangea during the Middle Permian, before becoming globally distributed during the Late Permian. Pareiasaurs were the largest reptiles of the Permian, reaching sizes equivalent to those of contemporary therapsids. Pareiasaurs became extinct in the Permian–Triassic extinction event.

Pareiasaurs ranged in size from 60 to 300 centimetres (2.0 to 9.8 ft) long, with some species estimated to exceed 1,000 kilograms (2,200 lb) in body mass.^[1][2] The limbs of many parieasaurs were extremely robust, likely to account for the increased stress on their limbs caused by their typically sprawling posture.^[1][2] The cow-sized Bunostegos differed from other pareiasaurs by having a more upright limb posture, being amongst the first amniotes to develop this trait.^[3] Pareiasaurs were protected by bony scutes called osteoderms that were set into the skin.^[4] Their skulls were heavily ornamented with bosses, rugose ridges, and bumps.^[5] Their leaf-shaped multi-cusped teeth resemble those of iguanas, indicating a herbivorous diet.^[6] The body probably housed an extensive digestive tract.^[1] Most authors have assumed a terrestrial lifestyle for pareiasaurs. A 2008 bone microanatomy study suggested a more aquatic, plausibly amphibious lifestyle,^[7] but a later 2019 study found that the bone histology provided no direct evidence of this lifestyle.^[8]

Pareiasaurs appear very suddenly in the fossil record. It is clear that these animals are parareptiles.^[9][10] As such, they are closely related to nycteroleterids.^[11] Pareiasaurs filled the large herbivore niche (orguild) that had been occupied early in the Permian period by the caseid pelycosaurs and, before them, the diadectid reptiliomorphs.^[8] They are much larger than the diadectids, more similar to the giant caseid pelycosaur Cotylorhynchus. Although the last Pareiasaurs were no larger than the first types (indeed, many of the last ones became smaller), there was a definite tendency towards increased armour as the group developed. Pareiasaurs first appeared in the fossil record in the Middle Permian (Guadalupian) of Southern Pangaea, before dispersing into Northern Pangaea and gaining a cosmopolitan distribution during the Late Permian (Lopingian).^[12]

Some paleontologists considered that pareiasaurs were direct ancestors of modern turtles. Pareiasaur skulls have several turtle-like features, and in some species the scutes have developed into bony plates, possibly the precursors of a turtle shell.^[13] Jalil and Janvier, in a large analysis of pareiasaur relationships, also found turtles to be close relatives of the "dwarf" pareiasaurs, such as Pumiliopareia.^[14] However, the discovery of Pappochelys argues against a potential pareisaurian relationship to turtles,^[15] and DNA evidence indicates that living turtles are more closely related to living archosaurs than lepidosaurs, and therefore cladistically diapsids.^[16]

Hallucicrania (Lee 1995): This clade was coined by MSY Lee for Lanthanosuchidae + (Pareiasauridae + Testudines). Lee's pareiasaur hypothesis has become untenable due to the diapsid features of the stem turtle Pappochelys and the potential testudinatan nature of Eunotosaurus. Recent cladistic analyses reveal that lanthanosuchids have a much more basal position in the Procolophonomorpha, and that the nearest sister taxon to the pareiasaurs are the rather unexceptional and conventional looking nycteroleterids (Müller & Tsuji 2007, Lyson et al. 2010) the two being united in the clade Pareiasauromorpha (Tsuji et al. 2012).

Pareiasauroidea (Nopcsa, 1928): This clade (as opposed to the superfamily or suborder Pareiasauroidea) was used by Lee (1995) for Pareiasauridae + Sclerosaurus. More recent cladistic studies place Sclerosaurus in the procolophonid subfamily Leptopleuroninae (Cisneros 2006, Sues & Reisz 2008), which means the similarities with pareiasaurs are the result of convergences.

Pareiasauria (Seeley, 1988): If neither Lanthanosuchidae or Testudines are included in the clade, the Pareiasauria only contains the monophyletic family Pareiasauridae.

Below is a cladogram from Tsuji et al. (2013):^[17]

• Carroll, R. L., (1988), Vertebrate Paleontology and Evolution, W.H. Freeman & Co. New York, p. 205
• Kuhn, O, 1969, Cotylosauria, part 6 of Handbuch der Palaoherpetologie (Encyclopedia of Palaeoherpetology), Gustav Fischer Verlag, Stuttgart & Portland
• Society of Vertebrate Paleontology (24 June 2013). "Pareiasaur: Bumpy beast was a desert dweller". ScienceDaily. Archived from the original on 2023-11-23. Retrieved 2024-03-01.

• "Introduction to Pareiasauria: An Upper Permian group of Anapsids". Ucmp.berkeley.edu. Archived from the original on 2023-09-27.
• "Hallucicrania [Pareiasauriformes]". Mikko's Phylogeny Archive. Archived from the original on 2007-12-09.
• "Anapsida: Hallucicrania". Palaeos. Archived from the original on 2005-04-09.