Scymnosaurus (σκύμνος skymnos 'lion cub' + σαῦρος, sauros 'lizard') is a dubious genus of therocephalian therapsids based upon various fossils of large early therocephalians. The genus was described by Robert Broom in 1903 with S. ferox, followed by S. watsoni in 1915 and a third, S. major, by Lieuwe Dirk Boonstra in 1954. Each of these species are considered nomen dubia today and based upon specimens belonging to two separate families of therocephalians. S. ferox and S. major represent specimens of Lycosuchidae incertae sedis, while S. watsoni is Scylacosauridae incertae sedis. Broom named a fourth species in 1907 from KwaZulu-Natal, S. warreni, though he later referred it to Moschorhinus as a valid species in 1932 but now is recognised as being synonymous with M. kitchingi.[1][2][3][4]
| Scymnosaurus Temporal range: Middle Permian-Triassic,
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| Holotype skull of S. watsoni (scylacosaurid incertae sedis) | |
Scientific classification 
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| Domain: | Eukaryota |
| Kingdom: | Animalia |
| Phylum: | Chordata |
| Clade: | Synapsida |
| Clade: | Therapsida |
| Clade: | †Therocephalia |
| Genus: | †Scymnosaurus Broom, 1903 (nomen dubium) |
| Species | |
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Scymnosaurus is estimated to have been approximately the size of the modern day hyena, and possessed teeth suggesting that it was carnivorous.[5] S. ferox was initially described as the second largest therocephalian, until the discovery of S. major, which is likely the largest therocephalian.[1][5][6]
It is notable that throughout the 19th century, Broom was involved with the work done with therocephalians and their classifications, and re-classifications, with paper and book publications ranging from 1903 to 1950.
Geology
editUnfortunately, in his initial description, Broom states the holotype fossil of S. ferox is from an unknown locality. This specimen, like many fossils of Scymnosaurus, is only of the anterior portion of the skull.[5]
Later Scymnosaurus fossils have been recovered and recorded as coming from the Tapinocephalus Assemblage Zone, many specifically from the Beaufort Group in South Africa. One specimen of S. ferox (SAM-PK-9084) and two S. major specimens, (SAM-PK-9005 and SAM-PK-10556) are from Beaufort West.[3] Prince Albert, an area southeast of the Beaufort group, produced one S. ferox fossil (SAM-PK-3430).[3]
The Beaufort group is a portion of the Karoo Basin Super group in South Africa. It represents from between 270-mya and 265ya to the middle of the Triassic.[7] The Tapinocephalus Assemblage Zone where Scymnosaurus fossils and other therapsids are found is the thickest layer of the Beaufort group. The Tapinocephalus AZ represents the middle Permian.
Chemical analyses of the sediment in the Beaufort group suggests that the climate changed from glacial to post-glacial in the Early Permian, creating a marine environment in the Karoo Basin. There is evidence this change in climate lead to a vegetation explosion, from soil acidity measurements. Moving into the middle Permian, the climate changed from a warm-humid climate to warm-arid, and the environment became terrestrial, supporting the Therapsids that are now found in the Tapinocephalus Assemblage Zone.[8]
History
editIn his 1903 publication, Broom argued for the establishment of a new taxon, Therocephalia, based on the palatal differences with Therapsida of three similar genera, Scylacosaurus, Ictidosaurus and Scymnosaurus. Therocephalia is still used as a descriptor to place some extinct Therapsids, However, Scymnosaurus has been moved into the Lycosuchidae incertae sedis.[1][3][5]
Scymnosaurus is still a name used for specimen today because it is the name that was applied to the holotype fossil.
S. watsoni was first classified coming from Lycosuchia, renamed as S. Watsoni, before being re-described as Lycosuchidae incertae sedis.[3][9]
Paleobiology
editDespite having only a partial fossil, it has been said that Scymnosaurs were likely not endothermic for the lack of a secondary palate. The higher metabolic load associated with endothermy is associated with characters such as fur, increased aerobic capacity and the development of a secondary palate, which allows for airflow independent of oral food processing.[10] It is, however, still unclear as to the order acquired characters that allowed the development of faster metabolisms, which happened at least twice with birds and mammals.[11][10]
S. ferox
editThe first of S. ferox, SAM-PK-632, from Broom's 1903 description, is of a partial snout and lower jaw tip. This species has been moved to Lycosuchidae.[5][3]
Dentition
editThe premaxilla carries five incisors each, and maxillary bones hold the canine and three molars. Broom notes that there is evidence of a lost secondary canine on one of the maxillary bones, due to the apparent remains of its root, almost filled in with spongy bone.[5] This second molar is later refuted as the remains of a baby tooth, which is also seen in Lycosuchidae.[3] The 3rd, 4th and 5th incisors have serrations, with increasing flatness toward the maxilla (5th being the flattest). The molars are sharp, flattened and have serrations on their posterior borders, suggesting a carnivorous diet.[5]
Palate
editThe internal nares is visible on the specimen, formed by the prevomers and palatine bones. According to Broom, which has since been refuted, the prevomers are wider than in Scylacosauridae. There is no indication of a secondary palate. Broom notes only the anterior portion of the pterygoid is present in the holotype specimen. The palatine bone forms a crest and lacks palatal dentition.
S. major
editS. major is possibly the largest Therocephalian, as there is enough of its skull preserved to give a measurement of 210 mm (8.3 in) for preorbital length. It has also been moved to Lycosuchidae incertae sedis. The holotype of S. major is SAM-10566.[1]
Dentition
editThe premaxillary bones have five incisors each, and maxillary bones hold two canines and one preserved post canine.[1]
Palate
editThere are minimal notes on skull characters as S. major skulls are "badly weathered".[1]
S. watsoni
editS. watsoni was initially described as an example of lycosuchidae, placed in Scymnosauridae by Broom in 1915, to be returned to Lycosuchidae incertae sedis.[1][12] The holotype fossil is BMNH R4100.[1]
Dentition
editLike S. ferox, it has five incisors, with a single canine followed by three preserved post canines.[12]
Palate/Post-orbital
editThe most notable features are large temporal fenestrae,[11] a narrow snout, and a high parietal crest.[1]
See also
edit
References
edit- ^ a b c d e f g h i J. Van Den Heever (1987), Dissertation Presented for the Degree of Doctor of Philosophy at the University of Stellenbosch
- ^ Groenewald, D. P.; Kammerer, C. F. (2023). "Re-identification and updated stratigraphic context of the holotypes of the late Permian tetrapods Dicynodon ingens and Scymnosaurus warreni from KwaZulu-Natal". Palaeontologia africana. 56: 171–179. hdl:10539/37143.
- ^ a b c d e f g Abdala, Fernando; Kammerer, Christian F.; Day, Michael O.; Jirah, Sifelani; Rubidge, Bruce S. (2014). "Adult morphology of the therocephalian Simorhinella baini from the middle Permian of South Africa and the taxonomy, paleobiogeography, and temporal distribution of the Lycosuchidae". Journal of Paleontology. 88 (6): 1139–1153. doi:10.1666/13-186. ISSN 0022-3360. S2CID 129323281.
- ^ Kammerer, C. F. (2023). "Revision of the Scylacosauridae (Therapsida: Therocephalia)". Palaeontologia Africana. 56: 51–87. hdl:10539/35700.
- ^ a b c d e f g Broom, Robert (1903). "On Some New Primitive Theriodonts". Annals of the South African Museum. 4.
- ^ LYDEKKER, R. (1908). "The Year's Vertebrate Palæontology". Science Progress in the Twentieth Century (1906-1916). 2 (7): 501–524. JSTOR 43776634.
- ^ Hancox, P.J; Rubidge, B.S (2001). "Breakthroughs in the biodiversity, biogeography, biostratigraphy, and basin analysis of the Beaufort group". Journal of African Earth Sciences. 33 (3–4): 563–577. doi:10.1016/s0899-5362(01)00081-1. ISSN 1464-343X.
- ^ Scheffler, Kay; Buehmann, Dieter; Schwark, Lorenz (2006-10-06). "Analysis of late Palaeozoic glacial to postglacial sedimentary successions in South Africa by geochemical proxies – Response to climate evolution and sedimentary environment". Palaeogeography, Palaeoclimatology, Palaeoecology. 240 (1–2): 184–203. doi:10.1016/j.palaeo.2006.03.059. ISSN 0031-0182.
- ^ Boonstra, L.D. (1969). "The Fauna Of The Tapinocephalus Zone (Beaufort Beds Of The Karoo)". Annals of the South African Museum Africa. 56: 50, 56.
- ^ a b Clarke, Andrew; Portner, Hans-Otto (2010). "Temperature, metabolic power and the evolution of endothermy". Biological Reviews. 85 (4): 703–727. doi:10.1111/j.1469-185X.2010.00122.x. PMID 20105154. S2CID 313909.
- ^ a b "Origin of Mammals Based Upon Cranial Morphology of the Therapsid Suborders. Geological Society of America Special Papers, Number 55.Everett C. Olson". The Quarterly Review of Biology. 20 (3): 269–270. September 1945. doi:10.1086/394899. ISSN 0033-5770.
- ^ a b Broom, Robert (1915). "On some new Carnivorous Therapsids in the Collection of the British Museum". Journal of Zoology. 85 (2): 163–173. doi:10.1111/j.1469-7998.1915.tb07409.x.