Pelycosaur

Pelycosaur (/ˈpɛlɪkəˌsɔːr/ PEL-ih-kə-sor)[1] is an older term for basal or primitive Late Paleozoic synapsids, excluding the therapsids and their descendants. Previously, the term mammal-like reptile had been used,[2] and pelycosaur was considered an order, but this is now thought to be incorrect, and seen as outdated.

Pelycosaurs
Temporal range: Pennsylvanian - Capitanian,
Mounted skeleton of Dimetrodon mileri, Harvard Museum of Natural History
Mounted skeleton of Dimetrodon mileri, Harvard Museum of Natural History
Scientific classificationEdit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Superclass: Tetrapoda
Clade: Reptiliomorpha
Clade: Amniota
Clade: Synapsida
Informal group: Pelycosauria
Cope, 1878
Groups included
Cladistically included but traditionally excluded taxa

Because it excludes the advanced synapsid group Therapsida, the term is paraphyletic and contrary to modern formal naming practice.[3] Thus the name pelycosaurs, similar to the term mammal-like reptiles, had fallen out of favor among scientists by the 21st century, and is only used informally, if at all, in the modern scientific literature.[4][5] The terms stem mammals, protomammals, and basal or primitive synapsids are used where needed, instead.

Etymology

The term pelycosaur has been fairly well abandoned by paleontologists because it no longer matches the features that distinguish a clade.[5] The modern word was created from Greek pélyx meaning 'wooden bowl' or 'axe' and saûros meaning 'lizard'. The intended etymology presents a problem, since pelycosaur as created basically means 'basin lizard', but there is a ambiguity between several original Greek words in that pélix is 'wooden bowl' and pelíkē is 'basin', whereas pélyx is 'ax' (like pélekys 'double-edged ax').

Pelycosauria is a paraphyletic taxon because it excludes the therapsids. For that reason, the term is sometimes avoided by proponents of a strict cladistic approach. Eupelycosauria is used to designate the clade that includes most pelycosaurs, along with the Therapsida and Mammalia. In contrast to "pelycosaurs", Eupelycosauria is a proper monophyletic group. Caseasauria is a pelycosaur side-branch, or clade, that did not leave any descendants.

Evolutionary history

Comparison of "pelycosaurian" skulls: 1 sphenacodont, 2 ophiacodont, 3 caseid. The quadratojugale is green, squamosale is red, jugale is blue.

The pelycosaurs appear to have been a group of synapsids that have direct ancestral links with the mammals, having differentiated teeth and a developing hard palate. The pelycosaurs appeared during the Late Carboniferous and reached their apex in the early part of the Permian, remaining the dominant land animals for some 40 million years. A few continued into the Capitanian, but they experienced a sharp decline in diversity in the late Kungurian.[6] They were succeeded by the therapsids.

Description

Some species were quite large, growing to a length of 3 metres (10 ft) or more, although most species were much smaller. Well-known pelycosaurs include the genera Dimetrodon, Sphenacodon, Edaphosaurus, and Ophiacodon.[7]

Pelycosaur fossils have been found mainly in Europe and North America, although some small, late-surviving forms are known from Russia and South Africa.

Unlike lepidosaurian reptiles, pelycosaurs lacked reptilian epidermal scales. Fossil evidence from some varanopids shows that parts of the skin were covered in rows of osteoderms, presumably overlain by horny scutes.[4] The belly was covered in rectangular scutes, looking like those present in crocodiles.[8] Parts of the skin not covered in scutes might have had naked, glandular skin like that found in some mammals. Dermal scutes are also found in a diverse number of extant mammals with conservative body types, such as in the tails of some rodents, sengis, moonrats, the opossums and other marsupials, and as regular dermal armour with underlying bone in the armadillo.

At least two pelycosaur clades independently evolved a tall sail, consisting of elongated vertebral spines: the edaphosaurids and the sphenacodontids. In life, this would have been covered by skin, and likely functioned as a thermoregulatory device[9] or as a mating display.

Taxonomy

Dimetrodon – a sphenacodontid

In phylogenetic nomenclature, "Pelycosauria" is not used formally, since it does not constitute a group of all organisms descended from some common ancestor (a clade), because the group specifically excludes the therapsids which are descended from pelycosaurs. Instead, it represents a paraphyletic "grade" of basal synapsids leading up to the clade Therapsida.[10]

In 1940, the group was reviewed in detail, and every species known at the time described, with many illustrated, in an important monograph by Alfred Sherwood Romer and Llewellyn Price.[11]

In traditional classification, the order Pelycosauria is paraphyletic in that the therapsids (the "higher" synapsids) have emerged from them. That means Pelycosauria is a grouping of animals that does not contain all descendants of its common ancestor, as is often required by phylogenetic nomenclature. In evolutionary taxonomy, Therapsida is a separated order from Pelycosauria, and mammals (having evolved from therapsids) are separated from both as their own class. This use has not been recommended by a majority of systematists since the 1990s,[5] but several paleontologists nevertheless continue using this word.[12][10]

The following classification was presented by Benton in 2004.[13]

See also

Notes

  1. Cope, E. D. (1878). "Descriptions of extinct Batrachia and Reptilia from the Permian formation of Texas". Proceedings of the American Philosophical Society. 17 (101): 505–530. JSTOR 982652.
  2. Carroll, R.L. 1988. Vertebrate Paleontology and Evolution. WH Freeman and Company, New York ISBN 0-7167-1822-7
  3. Hennig, Willi (1981). Insect phylogeny. Chichester [England]: J. Wiley. pp. xi + 514. ISBN 0471278483.
  4. Botha-Brink, J.; Modesto, S.P. (2007). "A mixed-age classed 'pelycosaur' aggregation from South Africa: Earliest evidence of parental care in amniotes?". Proceedings of the Royal Society B. 274 (1627): 2829–2834. doi:10.1098/rspb.2007.0803. PMC 2288685. PMID 17848370.
  5. Laurin, Michel (2010). How Vertebrates Left the Water. Berkeley, CA: University of California Press. pp. xv + 199. ISBN 978-0-520-26647-6.
  6. Didier, Gilles; Laurin, Michel (2021). "Distributions of extinction times from fossil ages and tree topologies: the example of some mid-Permian synapsid extinctions". PeerJ. 9 (e12577): e12577. doi:10.7717/peerj.12577. PMC 8667717. PMID 34966586.
  7. Cowen, Richard (2013). History of Life. John Wiley & Sons. pp. 91–92. ISBN 978-1-11851-093-3.
  8. Carroll, R.L. (1969). "Problems of the origin of reptiles". Biological Reviews. 44 (3): 393–432. doi:10.1111/j.1469-185X.1969.tb01218.x. S2CID 84302993.
  9. Tracy, C.R.; Turner, J.S.; Huey, R.B. (1986). "A biophysical analysis of possible thermoregulatoryadaptations in pelycosaurs". In MacLean, P.D.; Roth, J.J.; Roth, E.C.; Hotton, N. (eds.). Ecology and Biology of Mammal-Like Reptiles. Washington, DC: Smithsonian Press. pp. 195–205.
  10. Brocklehurst, Neil; Fröbisch, Jörg (2018). "A reexamination of Milosaurus mccordi, and the evolution of large body size in Carboniferous synapsids". Journal of Vertebrate Paleontology. 35 (8): e1508026. doi:10.1080/02724634.2018.1508026. S2CID 91487577.
  11. Romer, A.S.; Price, L.I. (1940). "Review of the Pelycosauria". 28 : Review of the Pelycosauria. Geological Society of America Special Papers. Vol. 28. pp. 1–538. doi:10.1130/SPE28-p1.
  12. Amson, Eli; Laurin, Michel (2011). "On the affinities of Tetraceratops insignis, an Early Permian synapsid". Acta Palaeontologica Polonica. 56 (2): 301–312. doi:10.4202/app.2010.0063. S2CID 56425905.
  13. Benton, Michael J. (2004). Vertebrate palaeontology (3rd ed.). Oxford: Blackwell Science. ISBN 978-0-632-05637-8.

References

  • Reisz, R.R. (1986). Handbuch der Paläoherpetologie [Encyclopedia of Paleoherpetology]. Verlag Dr. Friedrich Pfeil. Part 17A Pelycosauria. ISBN 3-89937-032-5.
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