Venyukovioidea

Last updated

Venyukovioidea
Temporal range: Middle - Late Permian, 267–260  Ma
Venyukovia1DB.jpg
Life restoration of Venyukovia prima
Scientific classification OOjs UI icon edit-ltr.svg
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Therapsida
Suborder: Anomodontia
Infraorder: Venyukovioidea
Watson and Romer, 1956
Genera

Venyukovioidea is an infraorder of anomodont therapsids related to dicynodonts from the Permian of Russia. They have also been known as 'Venjukovioidea', as well as by the similar names 'Venyukoviamorpha' or 'Venjukoviamorpha' in literature. This in part owes to a misspelling by Russian palaeontologist Ivan Efremov in 1940 when he mistakenly spelt Venyukovia , the namesake of the group, with a 'j' instead of a 'y' (i.e. 'Venjukovia'), which permeated through subsequent therapsid literature before the mistake was caught and corrected. [1] The order Ulemicia has also been coined for a similar taxonomic concept in Russian scientific literature, which notably excludes Suminia and Parasuminia . [2]

Contents

Venyukovioidea includes the genera Venyukovia, Otsheria , Ulemica , Suminia and Parasuminia, all from Western Siberia. [3] Historically, some of these genera have been placed in various families and subfamilies, including the Venyukoviidae/'Venjukoviidae', Otsheriidae, and Ulemiciidae. However, the internal lower-level relationships of the venyukovioids have not been fully resolved and so the utility and composition of these individual subgroups is unclear. Furthermore, although the group uses the '–oidea' suffix typical of superfamilies in Linnean taxonomy, it was originally coined as an infraorder by D. M. S. Watson and Alfred Romer in 1956. [4] Venyukovioidea was later cladistically defined by palaeontologists Christian F. Kammerer and Kenneth D. Angielczyk in 2009 as all anomodonts closer to Venyukovia than to Galeops or Dicynodon , distinguishing its contents from other anomodonts regarded as either 'dromasaurs' or dicynodonts. [1]

Description

Life restoration of Ulemica Ulemica092hair.jpg
Life restoration of Ulemica

Venyukovioidea was named for Venyukovia (in turn, named for that fossil's discoverer, Russian geologist P.N. Venyukov). [5] Venyukovia itself is known only from lower jaw fragments of a single individual, [6] [7] while Otsheria is only represented by a skull, Ulemica by its skull and lower jaws, and the fragmentary Parasuminia only by its jaw tips and part of the roof of the skull. [8] [9] Their skulls superficially resemble those of dicynodonts, with short snouts, large eyes and large temporal fenestrae, although by comparison they have relatively longer snouts and proportions resembling the basal anomodont Biseridens and (superficially) even dinocephalian therapsids. [10] [11] A curious feature of venyukovioids is that the pineal foramen (or "third eye") is surrounded by a raised "collar" or "chimney" of bone to varying degrees of development. [12]

To date, the only known venyukovioid post-cranial remains belong to the derived Suminia. [12] The comparatively long limbs and phalanges with opposable 'thumbs', as well as a long and potentially prehensile tail led to the suggestion that Suminia was adapted for grasping tree branches and lived an arboreal lifestyle. [8] [13]

Compared with other therapsids, venyukovioids are notable for their comparatively long tooth rows with large incisors and a lack of distinct canines. [14] The arrangement of teeth was complex and varied greatly among them. [15] Broadly, they had large and procumbent chisel-shaped incisors at the tips of both upper and lower jaws, [6] while "post-canine" teeth are noticeably smaller, and could be bulbous with sharp tips (Otsheria), bluntly conical (Ulemica) for grinding, or leaf-shaped and serrated for shredding (Suminia). [12] [16] Ulemica is notable for the presence of a short, bulbous caniniform in the middle of its maxilla, much larger than the surrounding peg-like teeth, while the dentition of Suminia is claimed to represent the first evidence of efficient chewing in tetrapods. [17] Ulemica has also been suggested to have had a partial horny covering on its lower jaw, based on the presence of pitting in the jaw bones and a shelf of bone lateral to the toothrow where the upper caniniform seemingly bit against. [16]

A notable aspect of venyukovioids is that they have a very similar jaw structure to the dicynodonts. This includes a wide zygomatic arch that bows upwards, allowing for the attachment of large jaw adductor muscles both inside the temporal fenestra and another on the outside attached beneath the arch (the external lateral adductor). Such a muscle is otherwise only found in dicynodonts proper among anomodonts. There is even a bony shelf of bone on the sides of the lower jaw for these muscles to attach to, very similar to the jaw muscle arrangement of dicynodonts. [10] [18] The jaw joint is also relatively long in venyukovioids, permitting it to slide backwards in a palinal stroke. This is only incipiently present in genera such as Ulemica, but is very well-developed in Suminia, which exhibits extensive sliding of the jaw in parallel with dicynodonts. It was once thought this was a shared trait between them, indicative of a close common ancestry. [12] However, the absence of such palinal chewing in other anomodonts potentially closer to dicynodonts (such as Patranomodon ) and its incipient development in less-derived venyukovioids (Ulemica) implies this was an example of convergent evolution as a similar adaptation to herbivory. [3] [19]

Classification and evolution

Venyukovioidea was historically regarded as one of two subdivisions of basal anomodonts along with the 'Dromasauria', with Venyukovioidea as a Laurasian group in the North and 'Dromasauria' as a southern radiation in Gondwana. Both groups were later suggested to be paraphyletic or even polyphyletic relative to each other and to dicynodonts, as proposed by Rubidge & Hopson in 1990, but phylogenetic studies have since borne out Venyukovioidea as a natural group after all ('dromasaurs' meanwhile appear to be genuinely polyphyletic). The cladogram below depicts an example of the paraphyletic interpretation of basal anomodont relationships from Rubidge and Hopson (1990), as modified by Rybczynski (2000) and with members of Venyukovioidea highlighted in green: [12]

Anomodontia

Patranomodon

Otsheria

Galeops

Ulemica

Dicynodontia

Although now consistently recognised as monophyletic and a genuine clade, the position of Venyukovioidea in the anomodont tree is not well settled. Initially, venyukovioids were thought to be the most "primitive" anomodonts, representing intermediate forms between derived dicynodonts and the dinocephalian form–as the two groups were sometimes thought to be closely related. [4] [20] As more early anomodonts were discovered at the end of the 20th century and computerised phylogenetic analyses were applied, Venyukovioidea were typically recovered as relatively more derived than both Biseridens and the anomocephaloids and grouped together in a clade with dicynodonts and taxa formerly included in 'Dromasauria' (i.e. Chainosauria). [1] [21] However, more recent analyses since 2017 have swapped this position, with venyukovioids being relatively more basal than anomocephaloids and occupying a more rootward position. [11]

Below are two cladograms depicting examples of these alternative positions. The cladogram on the left depicts Venyukovioidea as closer to dicynodonts (from Cisneros et al. (2015)), [22] while the right cladogram depicts them as more basal (from Angielczyk and Kammerer (2017)). [11] Note the incomplete sampling of venyukovioids in both trees, and the differing position of Suminia.

Cisneros et al. (2015): [22]

Anomodontia

Biseridens

Anomocephaloidea

Tiarajudens

Anomocephalus

Galechirus

Venyukovioidea

Otsheria

Suminia

Ulemica

Chainosauria

Patranomodon

Galeops

Dicynodontia

Angielczyk and Kammerer (2017): [11]

Anomodontia

Biseridens

Venyukovioidea

Suminia

Otsheria

Ulemica

Chainosauria

Galepus

Anomocephaloidea

Tiarajudens

Anomocephalus

Patranomodon

Galechirus

Galeops

Dicynodontia

Subsequently, the biogeographic origins and evolution of Venyukovioidea is also unclear. As the group is endemic to Russia, it was initially thought that they originated in the northern hemisphere. However, as more basal anomodonts were discovered in South Africa (such as Anomocephalus and Patranomodon), it was then suggested that anomodonts may have arisen in Gondwana, including the common ancestor of venyukovioids which later migrated to and radiated in Laurasia. [23] [24] Under their paraphyletic interpretation, Rubidge & Hopson (1990) suggested that there was a free exchange of anomodonts between the two hemispheres. [25] The subsequent identification of the Chinese therapsid Biseridens as the most basal known anomodont in 2009 lead Liu and colleagues to propose anomodonts had indeed originated in Laurasia before separating into two distinct radiations, Venyukovioidea in the North and a Southern radiation of chainosaurs, including the ancestral dicynodonts. [26]

Alternate taxonomies

In 2008, Russian palaeontologist Mikhaïl Ivakhnenko proposed an alternative taxonomic scheme for the taxa included in Venyukovioidea, as well as for anomodonts in general. He coined the order Ulemicia for Ulemica, Venyukovia and Otsheria, and further divided them into two families, Venyukoviidae and the monotypic Ulemicidae. Suminia (and later Parasuminia under this scheme), however, was not thought to be closely related to these 'ulemicians', unlike previous literature, and was instead referred to another family and order altogether, the Galeopidae. [2] [27] [28]

Galeopidae was initially coined for the South African 'dromasaur' Galeops by palaeontologist Robert Broom in 1912, but under Ivakhnenko's scheme was expanded to include other basal anomodonts, including Anomocephalus and Suminia. The family was included under a modified version of 'Dromasauria', Dromasaurida, which itself was regarded as a suborder of Dicynodontia ('true' dicynodonts were placed in the sister suborder Dicynodontida). Ivakhnenko divided the 'ulemicians' from dicynodonts (including 'dromasauridans') by the anatomy of their jaw joints, interpreting the well-developed sliding jaw joints of Suminia, Galeops and dicynodonts to indicate a closer relationships between them than to the 'ulemicians'. This opposes the typical phylogenetic interpretation of basal anomodont relationships and of Venyukovioidea, and has not been adopted outside of Russian literature. [1] [2] [27]

Related Research Articles

<span class="mw-page-title-main">Therapsid</span> Clade of tetrapods including mammals

A therapsid is a member of the clade Therapsida which is a major group of eupelycosaurian synapsids that includes mammals and their ancestors and relatives. Many of the traits today seen as unique to mammals had their origin within early therapsids, including limbs that were oriented more underneath the body, as opposed to the sprawling posture of many reptiles and salamanders.

<span class="mw-page-title-main">Dicynodont</span> Extinct clade of therapsids

Dicynodontia is an extinct clade of anomodonts, an extinct type of non-mammalian therapsid. Dicynodonts were herbivores that typically bore a pair of tusks, hence their name, which means 'two dog tooth'. Members of the group possessed a horny, typically toothless beak, unique amongst all synapsids. Dicynodonts first appeared in Southern Pangaea during the mid-Permian, ca. 270–260 million years ago, and became globally distributed and the dominant herbivorous animals in the Late Permian, ca. 260–252 Mya. They were devastated by the end-Permian Extinction that wiped out most other therapsids ca. 252 Mya. They rebounded during the Triassic but died out towards the end of that period. They were the most successful and diverse of the non-mammalian therapsids, with over 70 genera known, varying from rat-sized burrowers to elephant-sized browsers.

<span class="mw-page-title-main">Anomodont</span> Suborder of stem-mammals

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.

<i>Suminia</i> Extinct genus of therapsids

Suminia is an extinct genus of basal anomodont that lived during the Tatarian age of the late Permian, spanning approximately from 268-252 Ma. Suminia is recognized the youngest non-dicynodont anomodont. Its fossil localities are primarily derived from the Kotel’nich locality of the Kirov Oblast in Russia. However, there have been some isolated specimen found in a few different localities, all from eastern European regions of Russia.

<i>Diictodon</i> Extinct genus of dicynodonts

Diictodon is an extinct genus of pylaecephalid dicynodont that lived during the Late Permian period, approximately 255 million years ago. Fossils have been found in the Cistecephalus Assemblage Zone of the Madumabisa Mudstone of the Luangwa Basin in Zambia and the Tropidostoma Assemblage Zone of the Teekloof Formation, Tapinocephalus Assemblage Zone of the Abrahamskraal Formation, Dicynodon Assemblage Zone of the Balfour Formation, Cistecephalus Assemblage Zone of the Middleton or Balfour Formation of South Africa and the Guodikeng Formation of China. Roughly half of all Permian vertebrate specimens found in South Africa are those of Diictodon. This small herbivorous animal was one of the most successful synapsids in the Permian period.

<span class="mw-page-title-main">Dromasauria</span>

"Dromasaurs" are an artificial grouping of small anomodont therapsids from the Middle and Late Permian of South Africa. They represent either a paraphyletic grade or a polyphyletic grouping of small non-dicynodont basal anomodonts rather than a clade, and as such are considered an invalid group today. "Dromasaurs" were historically united by their superficially similar appearances that were unlike other known anomodonts. They are all small in size with slender limbs and long tails, and have short skulls with very large eye sockets. "Dromasauria" traditionally includes three genera, all from the Karoo Supergroup of South Africa: Galepus, Galechirus, and Galeops. These genera have sometimes been divided into two subgroups, the monotypic family Galeopidae and the Galechiridae for Galechiris and Galepus.

<i>Emydops</i> Extinct genus of dicynodonts

Emydops is an extinct genus of dicynodont therapsids from the Middle Permian to Late Permian of what is now South Africa. The genus is generally small and herbivorous, sharing the dicynodont synapomorphy of bearing two tusks. In the following years, the genus grew to include fourteen species. Many of these species were erected on the basis of differences in the teeth and the positioning of the frontal and parietal bones. A 2008 study narrowed Emydops down to two species, E. arctatus and the newly described E. oweni.

<i>Eodicynodon</i> Extinct genus of dicynodonts

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.

<i>Venyukovia</i> Extinct genus of therapsids

Venyukovia is an extinct genus of venyukovioid therapsid, a basal anomodont from the Middle Permian of Russia. The type and sole species, V. prima, is known only by a partial lower jaw with teeth. Venyukovia has often been incorrectly spelt as 'Venjukovia' in English literature. This stems from a spelling error made by Russian palaeontologist Ivan Efremov in 1940, who mistakenly replaced the 'y' with a 'j', which subsequently permeated through therapsid literature before the mistake was caught and corrected. Venyukovia is the namesake for the Venyukovioidea, a group of small Russian basal anomodonts also including the closely related Otsheria, Suminia, Parasuminia and Ulemica, although it itself is also one of the poorest known. Like other venyukovioids, it had large projecting incisor-like teeth at the front and lacked canines, although the remaining teeth are simple compared to some other venyukovioids, but may resemble those of Otsheria.

<i>Biseridens</i> Extinct genus of therapsids

Biseridens is an extinct genus of anomodont therapsid, and one of the most basal anomodont genera known. Originally known from a partial skull misidentified as an eotitanosuchian in 1997, another well-preserved skull was found in the Qingtoushan Formation in the Qilian Mountains of Gansu, China, in 2009 that clarified its relationships to anomodonts, such as the dicynodonts.

<i>Daptocephalus</i> Extinct genus of dicynodonts

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 Assemblage 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.

<i>Ulemica</i> Extinct genus of therapsids

Ulemica is an extinct genus of venyukovioid therapsids, a type of anomodont related to dicynodonts. It lived during the Middle Permian period in what is now Russia, and is known from the Isheevo assemblage of the Amanakskaya Formation. The type species, U. invisa, was originally placed in the genus Venyukovia by Russian palaeontologist Ivan Efremov in 1940. It was later given its own genus Ulemica in 1996 by Mikhaïl Ivakhnenko, who also named a second species U. efremovi. Efremov had originally intended to name the fossils of U. invisa as 'Myctosuchus invisus', however, he later recognised their similarity to Venyukovia and chose to assign the Isheevo material to this genus and leaving 'Myctosuchus' a nomen nudum.

<span class="mw-page-title-main">Chainosauria</span> Extinct clade of therapsids

Chainosauria is a large and speciose clade of anomodont therapsid that includes the highly diverse dicynodonts and a small number of closely related basal genera —although the total composition and taxonomic scope of Chainosauria is in flux. Chainosauria was named in 1923 to group together the dicynodonts and their close relatives, namely three small anomodont genera from South Africa that made up the now defunct group 'Dromasauria'. The name soon fell into disuse, however, as it was functionally replaced by Anomodontia. Chainosauria was later revived cladistically in 2009, preserving the association of dicynodonts and the 'dromasaurs' and has since served in effect as both a cladistic and a biogeographic counterpart to the Laurasian venyukovioids, with early chainosaurs appearing to have been a Gondwanan radiation.

<span class="mw-page-title-main">Pylaecephalidae</span> Extinct family of dicynodonts

Pylaecephalidae is a family of dicynodont therapsids that includes Diictodon, Robertia, and Prosictodon from the Permian of South Africa. Pylaecephalids were small burrowing dicynodonts with long tusks. The family was first named in 1934 and was redefined in 2009. Diictodontidae and Robertiidae are considered junior synonyms of Pylaecephalidae; although Pylaecephalus itself is considered a junior synonym of Diictodon, the name Pylaecephalidae predates these names and therefore takes priority.

<span class="mw-page-title-main">Therochelonia</span> Extinct clade of dicynodonts

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:

<span class="mw-page-title-main">Bidentalia</span> Extinct clade of dicynodonts

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.

Kunpania is an extinct genus of dicynodont therapsid from the Quanzijie Formation of Xinjiang, China. The type and only species is K. scopulusa, and it is known only by a single incomplete specimen including parts of the skull and forelimb. Since its initial description in 1978 by palaeontologist Ailing Sun, it has sometimes been considered to be another species of Dicynodon by other researchers, or potentially undiagnostic. However, a redescription in 2021 reaffirmed its distinctiveness, including a uniquely well developed muscle attachment on the humerus. Kunpania is perhaps the oldest known member of the derived dicynodont group Dicynodontoidea, potentially dating to the Middle Permian period during the Capitanian, and so may fill a knowledge gap in the history of dicynodont evolution.

<span class="mw-page-title-main">Anomocephaloidea</span> Extinct clade of therapsids

Anomocephaloidea is a clade of basal anomodont therapsids related to the dicynodonts known from what is now South Africa and Brazil during the Middle Permian. It includes only two species, Anomocephalus africanus from the Karoo Basin of South Africa and Tiarajudens eccentricus from the Paraná Basin of Brazil. Anomocephaloidea was named in 2011 with the discovery of Tiarajudens, although Anomocephalus itself has been known since 1999.

Parasumina is an extinct genus of anomodont known from the late Capitanian age at the end of the middle Permian period of European Russia. The type and only species is Parasuminia ivakhnenkoi. It was closely related to Suminia, another Russian anomodont, and was named for its resemblance. Little is known about Parasuminia as the only fossils are of fragmentary pieces of the skull and jaw, but the known remains suggest that its head and jaws were deeper and more robust than those of Suminia, and with shorter, stouter teeth. However, despite these differences they appear to have been similar animals with a similarly complex method of processing vegetation.

<i>Nyaphulia</i> Extinct genus of dicynodonts

Nyaphulia is an extinct genus of dicynodont therapsid from the middle Permian of South Africa, containing only the type species N. oelofseni. The generic name is in honour of John Nyaphuli of the National Museum of Bloemfontein, who contributed extensively to South African palaeontology and discovered the holotype specimen of Nyaphulia in 1982. Nyaphulia was initially named as a second species of the basal dicynodont Eodicynodon by Professor Bruce Rubidge in 1990 as E. oelofseni, named after his mentor in palaeontology and geology Dr. Burger Oelofsen.

References

  1. 1 2 3 4 Kammerer, C.F.; Angielczyk, K.D. (2009). "A proposed higher taxonomy of anomodont therapsids" (PDF). Zootaxa. 2018: 1–24. doi:10.11646/ZOOTAXA.2018.1.1.
  2. 1 2 3 Ivakhnenko, M. F. (2008). "Cranial morphology and evolution of Permian Dinomorpha (Eotherapsida) of eastern Europe". Paleontological Journal. 42: 859–995. doi:10.1134/S0031030108090013.
  3. 1 2 Angielczyk, Kenneth D.; Kammerer, Christian F. (2018). "Non-Mammalian synapsids: the deep roots of the mammalian family tree". In Zachos, Frank E.; Asher, Robert J. (eds.). Mammalian Evolution, Diversity and Systematics. Berlin: De Gruyter. p. 151. ISBN   9783110275902.
  4. 1 2 Watson, D. M. S.; Romer, A. S. (1956). "A classification of therapsid reptiles". Bulletin of the Museum of Comparative Zoology. 114 (2): 37–89.
  5. Ochev, V. G.; Surkov, M. V. (2000). "The history of excavation of Permo-Triassic vertebrates from Eastern Europe". In Benton, M. J.; Shishkin, M. A.; Unwin, D. M. (eds.). The Age of Dinosaurs in Russia and Mongolia. Cambridge University Press. pp. 1–16. ISBN   978-0-521-54582-2.
  6. 1 2 Battail, B; Surkov, M. V. (2000). "Mammal-like reptiles from Russia". In Benton, M. J.; Shishkin, M. A.; Unwin, D. M. (eds.). The Age of Dinosaurs in Russia and Mongolia. Cambridge University Press. pp. 86–119. ISBN   978-0-521-54582-2.
  7. Ivakhnenko, M. F. (1996). "Primitive anomodonts, venyukoviids, from the Late Permian of Eastern Europe". Paleontological Journal. 30: 575–582.
  8. 1 2 Fröbisch, J.; Reisz, R. R. (2011). "The postcranial anatomy of Suminia getmanovi (Synapsida: Anomodontia), the earliest known arboreal tetrapod". Zoological Journal of the Linnean Society. 162 (3): 661–698. doi: 10.1111/j.1096-3642.2010.00685.x .
  9. Kurkin, A. A. (2017). "A new Galeopid (Anomodontia, Galeopidae) from the Permian of Eastern Europe". Paleontological Journal . 51 (3): 308–312. doi:10.1134/S0031030117030042. S2CID   134828114.
  10. 1 2 Barghusen, H. R. (1976). "Notes on the adductor jaw musculature of Venjukovia, a primitive anomodont therapsid from the Permian of the USSR". Annals of the South African Museum. 69 (10): 249–260. ISBN   0949940933.
  11. 1 2 3 4 Angielczyk, K. D.; Kammerer, C. F. (2017). "The cranial morphology, phylogenetic position and biogeography of the upper Permian dicynodont Compsodon helmoedi van Hoepen (Therapsida, Anomodontia)". Papers in Palaeontology. 3 (4): 513–545. doi:10.1002/spp2.1087.
  12. 1 2 3 4 5 Rybczynski, N. (2000). "Cranial anatomy and phylogenetic position of Suminia getmanovi, a basal anomodont (Amniota: Therapsida) from the Late Permian of Eastern Europe". Zoological Journal of the Linnean Society. 130 (3): 329–373. doi: 10.1006/zjls.1999.0218 .
  13. Fröbisch, J.; Reisz, R. R. (2009). "The Late Permian herbivore Suminia and the early evolution of arboreality in terrestrial vertebrate ecosystems". Proceedings of the Royal Society B: Biological Sciences. 276 (1673): 3611–3618. doi:10.1098/rspb.2009.0911. ISSN   1471-2954. PMC   2817304 . PMID   19640883.
  14. Boonstra, L. D. (1971). "The early therapsids". Annals of the South African Museum. 59.
  15. Kemp, T. S. (2005). The Origin and Evolution of Mammals. Oxford University Press. pp. 39–42. ISBN   978-0-19-850761-1..
  16. 1 2 King, Gillian (1990). The Dicynodonts: A study in palaeobiology. London, New York: Chapman and Hall. pp. 66–68. ISBN   978-0-412-33080-3.
  17. Rybczynski, N.; Reisz, R. R. (2001). "Earliest evidence for efficient oral processing in a terrestrial herbivore". Nature. 411 (6838): 684–687. doi:10.1038/35079567. S2CID   4420916.
  18. King, G. M. (1994). "The early anomodont Venjukovia and the evolution of the anomodont skull". Journal of Zoology. 232 (4): 651–673. doi:10.1111/j.1469-7998.1994.tb04620.x.
  19. Angielczyk, K. D. (2004). "Phylogenetic evidence for and implications of a dual origin of propaliny in anomodont therapsids (Synapsida)". Paleobiology. 30 (2): 268–296. doi:10.1666/0094-8373(2004)030<0268:PEFAIO>2.0.CO;2. S2CID   86147610.
  20. King, G. M. (1988). Anomodontia. Encyclopedia of paleoherpetology, part 17C. Gustav Fischer. pp. 1–174. ISBN   0895742500.
  21. Kammerer, C. F.; Angielczyk, K. D.; Fröbisch, J. (2011). "A comprehensive taxonomic revision of Dicynodon (Therapsida, Anomodontia) and its implications for dicynodont phylogeny, biogeography, and biostratigraphy". Journal of Vertebrate Paleontology . 31 (Suppl. 1): 1–158. doi:10.1080/02724634.2011.627074.
  22. 1 2 Cisneros, J. C.; Abdala, F.; Jashashvili, T.; de Oliveira Bueno, A.; Dentzien-Dias, P. (2015). "Tiarajudens eccentricus and Anomocephalus africanus, two bizarre anomodonts (Synapsida, Therapsida) with dental occlusion from the Permian of Gondwana". Royal Society Open Science. 2 (7): 150090. Bibcode:2015RSOS....250090C. doi:10.1098/rsos.150090. PMC   4632579 . PMID   26587266.
  23. Rubidge, B. S.; Hopson, J. A. (1996). "A primitive anomodont therapsid from the base of the Beaufort Group (Upper Permian) of South Africa". Zoological Journal of the Linnean Society. 117: 115–139. doi:10.1111/j.1096-3642.1996.tb02152.x.
  24. Modesto, S.; Rubidge, B.; Welman, J. (1999). "The most basal anomodont therapsid and the primacy of Gondwana in the evolution of the anomodonts". Proceedings of the Royal Society of London B. 266 (1417): 331–337. doi:10.1098/rspb.1999.0642. PMC   1689688 .
  25. Rubidge, B. S.; Hopson, J. A. (1990). "A new anomodont therapsid from South Africa and its bearing on the ancestry of Dicynodontia". South African Journal of Science. 86 (1): 43–45.
  26. Liu, J.; Rubidge, B.; Li, J. "A new specimen of Biseridens qilianicus indicates its phylogenetic position as the most basal anomodont". Proceedings of the Royal Society B: Biological Sciences. 277 (1679): 285–92. doi:10.1098/rspb.2009.0883. PMC   2842672 . PMID   19640887.
  27. 1 2 Ivakhnenko, M. F. (2008). "The Subclass Theromorpha". In Ivakhnenko, M. F.; Kurochkin, E. N. (eds.). Iskopaemye pozvonochnye Rossii i sopredel’nykh stran. Iskopaemye reptilii i ptitsy. Chast’ 1 (Fossil Vertebrates of Russia and Adjacent Countries: Extinct Reptiles and Birds: Part 1) (in Russian). Moscow: GEOS. p. 158.
  28. Kurkin, A. A. (2017). "A new Galeopid (Anomodontia, Galeopidae) from the Permian of Eastern Europe". Paleontological Journal . 51 (3): 308–312. doi:10.1134/S0031030117030042.