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Therapsida

(Redirected from Therapsid)
Not to be confused with Theropsida.

Therapsida[a] is a clade comprising a major group of eupelycosaurian synapsids that includes mammals and their ancestors and close 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, resulting in a more "standing" quadrupedal posture, as opposed to the lower sprawling posture of many reptiles and amphibians.

Therapsida
Temporal range: Cisuralian–Holocene 279.5–0 Ma (Range includes mammals)
From top to bottom and left to right, several examples of non-mammalian therapsids: Biarmosuchus (Biarmosuchia), Moschops (Dinocephalia), Lystrosaurus (Anomodontia), Inostrancevia (Gorgonopsia), a lycosuchid (Therocephalia) and Chiniquodon (Cynodontia)
Scientific classification Edit this classification
Domain: Eukaryota
Kingdom: Animalia
Phylum: Chordata
Clade: Synapsida
Clade: Sphenacodontia
Clade: Pantherapsida
Clade: Sphenacodontoidea
Clade: Therapsida
Broom, 1905[1]
Clades

Therapsids evolved from earlier synapsids commonly called "pelycosaurs", specifically within the Sphenacodontia, more than 279.5 million years ago. They replaced the pelycosaurs as the dominant large land animals in the Guadalupian through to the Early Triassic. In the aftermath of the Permian–Triassic extinction event, therapsids declined in relative importance to the rapidly diversifying archosaurian sauropsids (pseudosuchians, dinosaurs and pterosaurs, etc.) during the Middle Triassic.

The therapsids include the cynodonts, the group that gave rise to mammals (Mammaliaformes) in the Late Triassic around 225 million years ago, the only therapsid clade that survived beyond the end of the Triassic. The only other group of therapsids to have survived into the Late Triassic, the dicynodonts, became extinct towards the end of the period. The last surviving group of non-mammaliaform cynodonts were the Tritylodontidae, which became extinct during the Early Cretaceous.

Characteristics

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Illustration of Alopecognathus, an early therocephalian therapsid

Jaw and teeth

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Therapsids' temporal fenestrae were larger than those of the pelycosaurs. The jaws of some therapsids were more complex and powerful, and the teeth were differentiated into frontal incisors for nipping, great lateral canines for puncturing and tearing, and molars for shearing and chopping food.

Posture

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Therapsid legs were positioned more vertically beneath their bodies than were the sprawling legs of reptiles and pelycosaurs. Also compared to these groups, the feet were more symmetrical, with the first and last toes short and the middle toes long, an indication that the foot's axis was placed parallel to that of the animal, not sprawling out sideways. This orientation would have given a more mammal-like gait than the lizard-like gait of the pelycosaurs.[2]

Physiology

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The physiology of therapsids is poorly understood. Most Permian therapsids had a pineal foramen, indicating that they had a parietal eye like many modern reptiles and amphibians. The parietal eye serves an important role in thermoregulation and the circadian rhythm of ectotherms, but is absent in modern mammals, which are endothermic.[3] Near the end of the Permian, dicynodonts, therocephalians and cynodonts show parallel trends towards loss of the pineal foramen, and the foramen is completely absent in probainognathian cynodonts. Evidence from oxygen isotopes, which are correlated with body temperature, suggests that most Permian therapsids were ectotherms and that endothermy evolved convergently in dicynodonts and cynodonts near the end of the Permian.[4] In contrast, evidence from histology suggests that endothermy is shared across Therapsida,[5] whereas estimates of blood flow rate and lifespan in the mammaliaform Morganucodon suggest that even early mammaliaforms had reptile-like metabolic rates.[6] Evidence for respiratory turbinates, which have been hypothesized to be indicative of endothermy, was reported in the therocephalian Glanosuchus, but subsequent study showed that the apparent attachment sites for turbinates may simply be the result of distortion of the skull.[7]

Integument

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The evolution of integument in therapsids is poorly known, and there are few fossils that provide direct evidence for the presence or absence of fur. The most basal synapsids with unambiguous direct evidence of fur are docodonts, which are mammaliaforms very closely related to crown-group mammals. Two "mummified" juvenile specimens of the dicynodont Lystrosaurus murrayi preserve skin impressions; the skin is hairless, leathery, and dimpled, somewhat comparable to elephant skin.[8][9] Fossilized facial skin from the dinocephalian Estemmenosuchus has been described as showing that the skin was glandular and lacked both scales and hair.[10]

Coprolites containing what appear to be hairs have been found from the Late Permian.[11][12] Though the source of these hairs is not known with certainty, they may suggest that hair was present in at least some Permian therapsids.

The closure of the pineal foramen in probainognathian cynodonts may indicate a mutation in the regulatory gene Msx2, which is involved in both the closure of the skull roof and the maintenance of hair follicles in mice.[13] This suggests that hair may have first evolved in probainognathians, though it does not entirely rule out an earlier origin of fur.[13]

Whiskers probably evolved in probainognathian cynodonts.[13][14] Some studies had inferred an earlier origin for whiskers based on the presence of foramina on the snout of therocephalians and early cynodonts, but the arrangement of foramina in these taxa actually closely resembles lizards,[15] which would make the presence of mammal-like whiskers unlikely.[14]

Evolutionary history

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See also: Evolution of mammals
 
Holotype skull of Raranimus dashankouensis, the most basal-known therapsid[16]

Therapsids evolved from a group of pelycosaurs called sphenacodonts.[17][18] Therapsids became the dominant land animals in the Middle Permian, displacing the pelycosaurs. Therapsida consists of four major clades: the dinocephalians, the herbivorous anomodonts, the carnivorous biarmosuchians, and the mostly carnivorous theriodonts. After a brief burst of evolutionary diversity, the dinocephalians died out in the later Middle Permian (Guadalupian) but the anomodont dicynodonts as well as the theriodont gorgonopsians and therocephalians flourished, being joined at the very end of the Permian by the first of the cynodonts.

 
Restoration of Euchambersia with dicynodont prey. Note that this South African therocephalian is suspected to be the oldest-known venomous tetrapod.[19]

Like all land animals, the therapsids were seriously affected by the Permian–Triassic extinction event, with the very successful gorgonopsians and the biarmosuchians dying out altogether and the remaining groups—dicynodonts, therocephalians and cynodonts—reduced to a handful of species each by the earliest Triassic. Surviving dicynodonts were represented by two families of disaster taxa (Lystrosauridae and Myosauridae), the scarcely known Kombuisia, and a single group of large stocky herbivores, the Kannemeyeriiformes, which were the only dicynodont lineage to thrive during the Triassic.[20] They and the medium-sized cynodonts (including both carnivorous and herbivorous forms) flourished worldwide throughout the Early and Middle Triassic. They disappear from the fossil record across much of Pangea at the end of the Carnian (Late Triassic), although they continued for some time longer in the wet equatorial band and the south.[citation needed]

Some exceptions were the still further derived eucynodonts.[21] At least three groups of them survived. They all appeared in the Late Triassic period. The extremely mammal-like family, Tritylodontidae, survived into the Early Cretaceous. Another extremely mammal-like family, Tritheledontidae, are unknown later than the Early Jurassic. Mammaliaformes was the third group, including Morganucodon and similar animals. Some taxonomists refer to these animals as "mammals", though most limit the term to the mammalian crown group.

 
Reconstruction of Bonacynodon schultzi, a probainognathian cynodont related to the ancestors of mammals[22]

The non-eucynodont cynodonts survived the Permian–Triassic extinction; Thrinaxodon, Galesaurus and Platycraniellus are known from the Early Triassic. By the Middle Triassic, however, only the eucynodonts remained.

The therocephalians, relatives of the cynodonts, managed to survive the Permian–Triassic extinction and continued to diversify through the Early Triassic period. Approaching the end of the period, however, the therocephalians were in decline to eventual extinction, likely outcompeted by the rapidly diversifying Saurian lineage of diapsids, equipped with sophisticated respiratory systems better suited to the very hot, dry and oxygen-poor world of the End-Triassic.

Dicynodonts were among the most successful groups of therapsids during the Late Permian, and survived through to near the end of the Triassic.

Mammals are the only living therapsids. The mammalian crown group, which evolved in the Early Jurassic period, radiated from a group of mammaliaforms that included the docodonts. The mammaliaforms themselves evolved from probainognathians, a lineage of the eucynodont suborder.

Classification

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Therapsida
The Hopson and Barghausen paradigm for therapsid relationships

Six major groups of therapsids are generally recognized: Biarmosuchia, Dinocephalia, Anomodontia, Gorgonopsia, Therocephalia and Cynodontia. A clade uniting therocephalians and cynodonts, called Eutheriodontia, is well supported, but relationships among the other four clades are controversial.[23] The most widely accepted hypothesis of therapsid relationships, the Hopson and Barghausen paradigm, was first proposed in 1986. Under this hypothesis, biarmosuchians are the earliest-diverging major therapsid group, with the other five groups forming the Eutherapsida, and within Eutherapsida, gorgonopsians are the sister taxon of eutheriodonts, together forming the Theriodontia. Hopson and Barghausen did not initially come to a conclusion about how dinocephalians, anomodonts and theriodonts were related to each other, but subsequent studies suggested that anomodonts and theriodonts should be classified together as the Neotherapsida. However, there remains debate over these relationships; in particular, some studies have suggested that anomodonts, not gorgonopsians, are the sister taxon of Eutheriodontia, other studies have found dinocephalians and anomodonts to form a clade, and both the phylogenetic position and monophyly of Biarmosuchia remain controversial.

In addition to the six major groups, there are several other lineages and species of uncertain classification. Raranimus from the early Middle Permian of China is likely to be the earliest-diverging known therapsid.[24] Tetraceratops from the Early Permian of the United States has been hypothesized to be an even earlier-diverging therapsid,[25][26] but more recent study has suggested it is more likely to be a non-therapsid sphenacodontian.[27]

Further information on the dubious genus of non-mammalian therapsid: Cynodraco

Biarmosuchia

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Main article: Biarmosuchia
 
Biarmosuchus, a biarmosuchian

Biarmosuchia is the most recently recognized therapsid clade, first recognized as a distinct lineage by Hopson and Barghausen in 1986 and formally named by Sigogneau-Russell in 1989. Most biarmosuchians were previously classified as gorgonopsians. Biarmosuchia includes the distinctive Burnetiamorpha, but support for the monophyly of Biarmosuchia is relatively low. Many biarmosuchians are known for extensive cranial ornamentation.

Dinocephalia

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Main article: Dinocephalia
 
Two genera of dinocephalians : Titanophoneus (an anteosaur) devouring a Ulemosaurus (a tapinocephalian)

Dinocephalia comprises two distinctive groups, the Anteosauria and Tapinocephalia.

Historically, carnivorous dinocephalians, including both anteosaurs and titanosuchids, were called titanosuchians and classified as members of Theriodontia, while the herbivorous Tapinocephalidae were classified as members of Anomodontia.

Anomodontia

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Main article: Anomodontia
 
Lystrosaurus, a dicynodont anomodont

Anomodontia includes the dicynodonts, a clade of tusked, beaked herbivores, and the most diverse and long-lived clade of non-cynodont therapsids. Other members of Anomodontia include Suminia, which is thought to have been a climbing form.

Gorgonopsia

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Main article: Gorgonopsia
 
Inostrancevia, a gorgonopsian

Gorgonopsia is an abundant but morphologically homogeneous group of saber-toothed predators.

Therocephalia

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Main article: Therocephalia
 
Moschorhinus, a therocephalian

It has been suggested that Therocephalia might not be monophyletic, with some species more closely related to cynodonts than others.[28] However, most studies regard Therocephalia as monophyletic.

Cynodontia

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Main article: Cynodontia
 
Trucidocynodon, a non-mammalian cynodont

Cynodonts are the most diverse and longest-lived of the therapsid groups, as Cynodontia includes mammals. Cynodonts are the only major therapsid clade to lack a Middle Permian fossil record, with the earliest-known cynodont being Charassognathus from the Wuchiapingian age of the Late Permian. Non-mammalian cynodonts include both carnivorous and herbivorous forms.

See also

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Notes

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  1. ^ Greek: 'beast-arch'

References

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  1. ^ Broom, R. (1905). "On the use of the term Anomodontia". Records of the Albany Museum. 1 (4): 266–269.
  2. ^ Carroll, R. L. (1988). Vertebrate Paleontology and Evolution. New York: W. H. Freeman and Company. pp. 698. ISBN 978-0-7167-1822-2.
  3. ^ Benoit, Julien; Abdala, Fernando; Manger, Paul; Rubidge, Bruce (2016). "The sixth sense in mammalians forerunners: variability of the parietal foramen and the evolution of the pineal eye in South African Permo-Triassic eutheriodont therapsids". Acta Palaeontologica Polonica. doi:10.4202/app.00219.2015. ISSN 0567-7920. S2CID 59143925.
  4. ^ Rey, Kévin; Amiot, Romain; Fourel, François; Abdala, Fernando; Fluteau, Frédéric; Jalil, Nour-Eddine; Liu, Jun; Rubidge, Bruce S; Smith, Roger MH; Steyer, J Sébastien; Viglietti, Pia A; Wang, Xu; Lécuyer, Christophe (18 July 2017). "Oxygen isotopes suggest elevated thermometabolism within multiple Permo-Triassic therapsid clades". eLife. 6: –28589. doi:10.7554/eLife.28589. ISSN 2050-084X. PMC 5515572. PMID 28716184.
  5. ^ Faure-Brac, Mathieu G.; Cubo, Jorge (2 March 2020). "Were the synapsids primitively endotherms? A palaeohistological approach using phylogenetic eigenvector maps". Philosophical Transactions of the Royal Society B: Biological Sciences. 375 (1793): 20190138. doi:10.1098/rstb.2019.0138. ISSN 1471-2970. PMC 7017441. PMID 31928185.
  6. ^ Newham, Elis; Gill, Pamela G.; Brewer, Philippa; Benton, Michael J.; Fernandez, Vincent; Gostling, Neil J.; Haberthür, David; Jernvall, Jukka; Kankaanpää, Tuomas; Kallonen, Aki; Navarro, Charles; Pacureanu, Alexandra; Richards, Kelly; Brown, Kate Robson; Schneider, Philipp; Suhonen, Heikki; Tafforeau, Paul; Williams, Katherine A.; Zeller-Plumhoff, Berit; Corfe, Ian J. (2020). "Reptile-like physiology in Early Jurassic stem-mammals". Nature Communications. 11 (1): 5121. Bibcode:2020NatCo..11.5121N. doi:10.1038/s41467-020-18898-4. ISSN 2041-1723. PMC 7550344. PMID 33046697.
  7. ^ Hopson, James A. (18 October 2012). "The Role of Foraging Mode in the Origin of Therapsids: Implications for the Origin of Mammalian Endothermy". Fieldiana Life and Earth Sciences. 5: 126–148. doi:10.3158/2158-5520-5.1.126. ISSN 2158-5520. S2CID 84471370.
  8. ^ Smith, Roger M.H.; Botha, Jennifer; Viglietti, Pia A. (15 October 2022). "Taphonomy of drought afflicted tetrapods in the Early Triassic Karoo Basin, South Africa". Palaeogeography, Palaeoclimatology, Palaeoecology. 604: 111207. Bibcode:2022PPP...60411207S. doi:10.1016/j.palaeo.2022.111207.
  9. ^ Timmons, Jeanne (20 September 2022). "These Fossil Mummies Reveal a Brutal World Long Before T. Rex Lived". Gizmodo. Retrieved 25 July 2024.
  10. ^ Chudinov, P. K. (1968). "Structure of the integuments of theromorphs". Doklady Akad. Nauk SSSR. 179: 226–229.
  11. ^ Smith, Roger M.H.; Botha-Brink, Jennifer (2011). "Morphology and composition of bone-bearing coprolites from the Late Permian Beaufort Group, Karoo Basin, South Africa". Palaeogeography, Palaeoclimatology, Palaeoecology. 312 (1–2): 40–53. Bibcode:2011PPP...312...40S. doi:10.1016/j.palaeo.2011.09.006. ISSN 0031-0182.
  12. ^ Bajdek, Piotr; Qvarnström, Martin; Owocki, Krzysztof; Sulej, Tomasz; Sennikov, Andrey G.; Golubev, Valeriy K.; Niedźwiedzki., Grzegorz (2016). "Microbiota and food residues including possible evidence of pre-mammalian hair in Upper Permian coprolites from Russia". Lethaia. 49 (4): 455–477. Bibcode:2016Letha..49..455B. doi:10.1111/let.12156.
  13. ^ a b c Benoit, J.; Manger, P. R.; Rubidge, B. S. (9 May 2016). "Palaeoneurological clues to the evolution of defining mammalian soft tissue traits". Scientific Reports. 6 (1): 25604. Bibcode:2016NatSR...625604B. doi:10.1038/srep25604. ISSN 2045-2322. PMC 4860582. PMID 27157809.
  14. ^ a b Benoit, Julien; Ruf, Irina; Miyamae, Juri A.; Fernandez, Vincent; Rodrigues, Pablo Gusmão; Rubidge, Bruce S. (2020). "The Evolution of the Maxillary Canal in Probainognathia (Cynodontia, Synapsida): Reassessment of the Homology of the Infraorbital Foramen in Mammalian Ancestors". Journal of Mammalian Evolution. 27 (3): 329–348. doi:10.1007/s10914-019-09467-8. ISSN 1573-7055. S2CID 156055693.
  15. ^ Estes, Richard (1961). "Cranial anatomy of the cynodont reptile Thrinaxodon liorhinus". Bulletin of the Museum of Comparative Zoology. 125: 165–180.
  16. ^ Liu, Jun; Rubidge, Bruce; and Li, Jinling (2009). "New basal synapsid supports Laurasian origin for therapsids" (PDF). Acta Palaeontologica Polonica. 54 (3): 393–400. doi:10.4202/app.2008.0071. Retrieved 25 September 2009.
  17. ^ Synapsid Classification & Apomorphies
  18. ^ Huttenlocker, Adam K. and Rega, Elizabeth (2012). "Chapter 4. The Paleobiology and Bone Microstructure of Pelycosauriangrade Synapsids". In Chinsamy-Turan, Anusuya (ed.). Forerunners of Mammals: Radiation, Histology, Biology. Indiana University Press. pp. 90–119. ISBN 978-0253005335.
  19. ^ Benoit, Julien; Norton, Luke A.; Manger, Paul R.; and Rubidge, Bruce S. (2017). Claessens, Leon (ed.). "Reappraisal of the envenoming capacity of Euchambersia mirabilis (Therapsida, Therocephalia) using μCT-scanning techniques". PLOS ONE. 12 (2): e0172047. Bibcode:2017PLoSO..1272047B. doi:10.1371/journal.pone.0172047. PMC 5302418. PMID 28187210.
  20. ^ Kammerer, Christian F.; Fröbisch, Jörg; Angielczyk, Kenneth D. (31 May 2013). Farke, Andrew A. (ed.). "On the Validity and Phylogenetic Position of Eubrachiosaurus browni, a Kannemeyeriiform Dicynodont (Anomodontia) from Triassic North America". PLOS ONE. 8 (5): e64203. Bibcode:2013PLoSO...864203K. doi:10.1371/journal.pone.0064203. ISSN 1932-6203. PMC 3669350. PMID 23741307.
  21. ^ Padian, Kevin (4 September 2013). "A Review of "Forerunners of Mammals: Radiation, Histology, Biology"". Journal of Vertebrate Paleontology. 33 (5): 1250–1251. Bibcode:2013JVPal..33.1250P. doi:10.1080/02724634.2013.763814. ISSN 0272-4634.
  22. ^ Geggel, L. (2016). "Meet the Ancient Reptile that Gave Rise to Mammals". Scientific American.
  23. ^ Angielczyk, Kenneth D.; Kammerer, Christian F. (22 October 2018). "Non-Mammalian synapsids: the deep roots of the mammalian family tree". In Zachos, Frank; Asher, Robert (eds.). Mammalian Evolution, Diversity and Systematics. De Gruyter. pp. 117–198. doi:10.1515/9783110341553-005. ISBN 978-3-11-034155-3. S2CID 92370138.
  24. ^ Duhamel, A.; Benoit, J.; Rubidge, B. S. & Liu, J. (August 2021). "A re-assessment of the oldest therapsid Raranimus confirms its status as a basal member of the clade and fills Olson's gap". The Science of Nature. 108 (4): 26. Bibcode:2021SciNa.108...26D. doi:10.1007/s00114-021-01736-y. ISSN 0028-1042. PMID 34115204. S2CID 235403632.
  25. ^ Laurin, M.; Reisz, R. R. (1996). "The osteology and relationships of Tetraceratops insignis, the oldest known therapsid". Journal of Vertebrate Paleontology. 16 (1): 95–102. Bibcode:1996JVPal..16...95L. doi:10.1080/02724634.1996.10011287.
  26. ^ 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. ISSN 0567-7920. S2CID 56425905.
  27. ^ Spindler, Frederik (2020). "The skull of Tetraceratops insignis (Synapsida, Sphenacodontia)". Palaeovertebrata. 43 (1): e1. doi:10.18563/pv.43.1.e1. S2CID 214247325.
  28. ^ Abdala, Fernando; Rubidge, Bruce S.; van den Heever, Juri (2008). "The oldest therocephalians (Therapsida, Eutheriodontia) and the early diversification of Therapsida". Palaeontology. 51 (4): 1011–1024. Bibcode:2008Palgy..51.1011A. doi:10.1111/j.1475-4983.2008.00784.x. ISSN 1475-4983. S2CID 129791548.

Further reading

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  • Benton, M. J. (2004). Vertebrate Palaeontology, 3rd ed., Blackwell Science.
  • Carroll, R. L. (1988). Vertebrate Paleontology & Evolution. W. H. Freeman & Company, New York.
  • Kemp, T. S. (2005). The origin and evolution of mammals. Oxford University Press.
  • Romer, A. S. (1966). Vertebrate Paleontology. University of Chicago Press, 1933; 3rd ed.
  • Bennett, A. F., & Ruben, J. A. (1986). "The metabolic and thermoregulatory status of therapsids." In The ecology and biology of mammal-like reptiles. Smithsonian Institution Press, Washington, DC, 207-218.
  • Kammerer, Christian F.; Angielczyk, Kenneth D.; Fröbisch, Jörg (2014). Early Evolutionary History of the Synapsida. Vertebrate Paleobiology and Paleoanthropology. Bibcode:2014eehs.book.....K. doi:10.1007/978-94-007-6841-3. ISBN 978-94-007-6840-6.
  • Ross, R.P., Ross, C.A. (2023). Permian Period, geochronology. Encyclopedia Britannica. https://www.britannica.com/science/Permian-Period
  • Padian, Kevin (2013-09). "A Review of "Forerunners of Mammals: Radiation, Histology, Biology"". Journal of Vertebrate Paleontology. 33 (5): 1250–1251.
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