Palaeontologia africana
Permanent URI for this communityhttps://wiredspace.wits.ac.za/handle/10539/13253
ISSN (print): 0078-8554
ISSN (electronic): 2410-4418
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Item A new middle Permian burnetiamorph (Therapsida: Biarmosuchia) from the South African Karoo filling a gap in the biarmosuchian record(The Evolutionary Studies Institute, 2024-09) Matlhaga, Fonda; Benoit, Julien; Rubidge, Bruce SBiarmosuchia, the most basal therapsid clade, is represented by relatively few specimens known from Permian deposits in Russia and southern Africa. In both the Guadalupian (middle Permian) and Lopingian (late Permian), biarmosuchians represent less than 1% of the fossil record at the specimen level. Here, we describe a new burnetiamorph biarmosuchian, Impumlophantsi boonstrai, based on a partial skull and associated postcrania from the upper Tapinocephalus Assemblage Zone. It is characterized by the presence of a low nasal crest with a unique morphology among burnetiamorphs. Inclusion of this taxon in an updated phylogenetic analysis of biarmosuchians indicates that this specimen is one of the most basal burnetiamorphs, representing the only record of this grade from the middle Permian.Item Craniomandibular anatomy of the akidnognathid therocephalian Olivierosuchus parringtoni from the Early Triassic of South Africa(Evolutionary Studies Institute, 2023) Gigliotti, Alessandro; Pusch, Luisa C; Kammerer, Christian F; Benoit, Julien; Fröbisch, JörgTherocephalians were an ecomorphologically varied and diverse-sized group of therapsids with widespread distribution during the late Permian and earliest Triassic periods. Here, we redescribe the holotype of the therocephalian Olivierosuchus parringtoni (BP/1/3849) from the Early Triassic Lystrosaurus declivis Assemblage Zone in the main Karoo Basin of South Africa. The specimen includes a complete skull, mandible, and the anterior portion of the skeleton. Previously unknown endocranial features are described using high-resolution computed tomography (CT), including internal surfaces of braincase and palatal bones, as well as soft tissue structures such as the brain and inner ear endocasts. Comparisons with closely related therapsids permit a detailed comparative analysis of the brain and inner ear morphology of Olivierosuchus.Item First occurrence of the dicynodont Digalodon (Therapsida, Anomodontia) from the Lopingian upper Madumabisa Mudstone Formation, Luangwa Basin, Zambia(Evolutionary Studies Institute, 2019-04) Angielczyk, Kenneth D.Digalodon is a rare emydopoid dicynodont first described from upper Permian rocks in the Karoo Basin of South Africa. During fieldwork in the upper Madumabisa Mudstone Formation of the Luangwa Basin (Zambia) in 2014, a small dicynodont skull was discovered that conforms very well to the recently revised diagnosis of Digalodon rubidgei, although some minor differences between the Zambian and South African specimens are apparent. The Zambian occurrence of Digalodon expands the known geographic range of the genus, which was previously limited to a small set of localities in the vicinity of the town of Graaff-Reinet (Eastern Cape). Based on historical specimens, Digalodon is thought to have a comparatively short stratigraphic range in the Balfour Formation that spans the boundary between the Cistecephalus and Daptocephalus assemblage zones. This observation may allow refinement of biostratigraphic correlations between the Karoo and Luangwa Basins, but discovery of more precisely-provenanced specimens in the Karoo is needed to fully assess Digalodon’s biostratigraphic utility.Item A new dicynodont (Anomodontia: Emydopoidea) from the terminal Permian of KwaZulu-Natal, South Africa(Evolutionary Studies Institute, 2019-04) Kammerer, Christian F.A new taxon of dicynodont (Thliptosaurus imperforatus gen. et sp. nov.) is described based on a dorsoventrally-crushed skull from latest Permian (upper Daptocephalus Assemblage Zone) strata in KwaZulu-Natal, South Africa. Thliptosaurus is distinguished from all other dicynodonts by an elongate intertemporal bar with broad dorsal exposure of the parietals but apparently no pineal foramen. Absence of the pineal foramen in dicynodonts is exceedingly rare; the only other taxa which exhibit this feature either have substantially broader (Kawingasaurus fossilis) or narrower (Kombuisia frerensis) intertemporal regions. Inclusion of Thliptosaurus in a phylogenetic analysis of dicynodonts recovers it as a kingoriid emydopoid, a position supported by its anteriorly-restricted pterygoid keel, elongate, curved anterior process of the lacrimal, relatively posterior position of the median pterygoid plate, and occlusion of the mandibular fenestra by a lateral plate of the dentary. Intriguingly, even in the other kingoriids which retain a pineal foramen (Dicynodontoides spp. and Kombuisia antarctica), this structure is reduced in size relative to other dicynodonts, suggesting that the pineal eye was less important for thermoregulatory activity in this clade than in other anomodonts. Although part of a local fauna including taxa that are otherwise widespread in the Karoo Basin (Daptocephalus, Lystrosaurus), the unique presence of Thliptosaurus in the relatively poorly-sampled Daptocephalus Assemblage Zone deposits of KwaZulu-Natal suggests that this region may preserve endemic taxa, and should be prioritized for future fieldwork.Item The first skeletal evidence of a dicynodont from the lower Elliot Formation of South Africa(Evolutionary Studies Institute, 2018) Kammerer, Christian F.Historical fossil specimens from the lower Elliot Formation are identified as representing a large-bodied dicynodont, the first known from skeletal material in the Late Triassic of South Africa. Although fragmentary, these fossils differ from all other known Triassic dicynodonts and are here described as a new taxon, Pentasaurus goggai gen. et sp. nov. Pentasaurus can be distinguished from other Triassic dicynodonts by a number of mandibular characters, most importantly the well-developed, unusually anteriorly-positioned lateral dentary shelf. Phylogenetic analysis indicates that Pentasaurus is a placeriine stahleckeriid. Placeriines include the latestsurviving dicynodonts but their remains are primarily known from the Northern Hemisphere, with their only previously-known Southern Hemisphere representative being the Middle Triassic Zambian taxon Zambiasaurus. The discovery of a placeriine in the Late Triassic of SouthAfrica supports recent proposals that local climatic conditions, not broad-scale biogeographic patterns, best explain the observed distribution of Triassic tetrapods. The tetrapod fauna of the lower Elliot Formation is highly unusual among Triassic assemblages in combining ‘relictual’ taxa like dicynodonts and gomphodont cynodonts with abundant, diverse sauropodomorph dinosaurs.Item Rediscovery of the holotype of Clelandina major Broom, 1948 (Gorgonopsia: Rubidgeinae) with implications for the identity of this species(Evolutionary Studies Institute, 2017-12) Kammerer, Christian F.No specimen number was given for the holotype of the rubidgeine gorgonopsian species Clelandina major Broom, 1948 in its original description. Historically, a specimen in the Rubidge Collection (RC 94) was considered to represent Broom’s type specimen for C. major. However, recent study has revealed that the holotype of C. major is in fact a different specimen in the McGregor Museum in Kimberley (MMK 5031). The morphology of this specimen is consistent with the genus Clelandina, contra work based on RC 94 that considered C. major referable toAelurognathus. Clelandina major is here considered synonymous with the type species Clelandina rubidgei.MMK5031 represents only the fifth known specimen of this rare and unusual gorgonopsian.Item Two unrecognised burnetiamorph specimens from historic Karoo collections(2016-03) Kammerer, Christian F.Two historical specimens from Permian rocks of the Karoo Basin represent previously unrecognised members of the rare therapsid group Burnetiamorpha. These specimens cannot be referred to any existing burnetiamorph species, but are left in open nomenclature because of their incompleteness (both are isolated skull roofs). The first specimen is from the Tapinocephalus Assemblage Zone (AZ) and is characterized by heavily pachyostosed supraorbital bosses and a low nasal crest. The second specimen is from the Tropidostoma AZ and is generally similar to the Malawian taxon Lende, but is unique among described burnetiamorphs in having a frontoparietal ‘dome’ that surrounds the pineal foramen. Phylogenetic analysis of burnetiamorphs recovers support for a split between Proburnetia and Burnetia-like burnetiids, here named Proburnetiinae subfam. nov. and Burnetiinae Broom, 1923.