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Tapinocaninus

Tapinocaninus is an extinct genus of therapsids in the family Tapinocephalidae, of which it is the most basal member. Only one species is known, Tapinocaninus pamelae. The species is named in honor of Rubidge's mother, Pamela. Fossils have been found dating from the Middle Permian.

Discovery
Tapinocaninus fossils were first found in the Eodicynodon Assemblage Zone of the Karoo deposits, in the Lower Beaufort Beds in Beaufort West. Five specimens are known, four found at Modderdrift farm and one found on Swartgrond farm. A holotype (NMQR 2987) and four paratypes (NMQR 2985, 2986, 3097 and ROZ K95). Prior to the discovery of the Tapinocaninus, the Anteosaurinae were believed to be the most primitive dinocephalians, and the Tapinocephalinae were believed to be the most derived dinocephalians of South Africa. When comparing features of Tapinocaninus to those discussed of Tapinocephalinae through a cladistic analysis, Rubidge et al. (1991) found that a synapomorphy of the two were the expanded heels on the incisor teeth. Thus, after its discovery, Tapinocaninus is considered the most primitive tapinocephaline. ==Description==
Description
This species is known from several skulls, as most specimens found were lacking of the post cranial skeleton. It was a large animal, measuring 2.5m in length from snout to ilium. Tapinocaninus were also the largest therapsids from the Guadalupian. Skull The skull roof and postorbital bar of Tapinocaninus shows pachyostotic thickening, which is consistent with other tapinocephaline dinocephalians. The skull roof is majorly composed of the frontal, which extends between the orbital and temporal fenestre. The external naris is bordered dorsally, anteriorly, and anteroventrally by the premaxilla bone. The maxilla forms a majority of the lateral area of the face, and it is swollen to allow room for the root of the canine tooth. The temporal openings are relatively large, and subsequently, Tapinocaninus has a narrow intertemporal region, which is considered a primitive feature of Tapinocephalinae. The temporal fenestra are bordered ventrally and posteriorly by the squamosal, and dorsally by the postorbital. The squamosal and postorbital touch along the temporal opening, which is a feature commonly found in tapinocephalids. Additionally, these taxon have a thin snout, sloping occipital, relatively small quadratojugal, prominent stapedial foramen, and relatively anterior position of the quadrate. The presence of only two sacral vertebrae in Tapinocaninus differs from other therapsids, such as Moschops which has three. Ribs There are ribs present along the entire vertebral column. In the cervical region, the ribs are shortened and flat. The longest ribs are present in the mid-dorsal region, and dorsal ribs 11-15 are barrel shaped to accommodate the large digestive system of Tapinocaninus. In the caudal region, the ribs are again shortened, in addition to being dorsoventrally flattened, posteriorly directed, and not fused to the caudal vertebrae Femur The holotype NMQR 2987 has both the left and right femora present. This specimen shows that the femur is more slender than the humerus. The femur is the same width at the proximal and distal ends, and it is flattened anteroposteriorly. Similar to other tapinocephalids, Tapinocaninus has a medially inflected femoral head. At the distal end of the femur, there are lateral and medial condyles, and the lateral condyle is slightly larger in size. Dentition Although there is currently no specimen with perfectly preserved teeth, the dental description for Tapinocaninus has been drawn from various skulls (NMQR 2984, NMQR 2986, NMQR 2987, ROZ K95).This dinocephalian has a heterodont dentition, consisting of incisors, canines and post canines. There are a maximum of five incisor teeth present in the premaxilla, all of which display talon and heel morphology. A singular canine is the first tooth in the maxilla bone, it is curved backward, and does not have a heel. Following the canine is the post canine teeth, characterized by pointed crowns and small, lingually situated heels. The dentition indicates that these animals were likely an herbivore or omnivore. == Paleobiology ==
Paleobiology
Posture and locomotion Researchers suggest the forelimb posture of Tapinocaninus to be “intermediate” between sprawling and an upright posture. It is suggested that they are more upright standing than sphenacodonts, but more sprawled than theriodont therapsids. Their intermediate posture can be explained by their long bones, in addition to the shape and positioning of the humerus and medially inflected femur. This postural stance would also be more supportive of the Tapinocaninus’ larger body size. Feeding Heterodont dentition indicates that the teeth are morphologically differentiated by shape. In Tapinocaninus, this includes incisors, canines, and postcanines, all of which have different shapes which allows for a variety of functions. Tapinocaninus was likely an herbivore or an omnivore. == Geological and biostratigraphic information ==
Geological and biostratigraphic information
The Eodicynodon Assemblage Zone is in the southwestern part of the Karoo Basin, and it is the lowest biozone of the Beaufort Group, under the Eosimops-Glanosuchus Subzone of the Tapinocephalus Assemblage Zone. The lower boundary lies at a stratigraphic horizon between the Ecca Group (Waterford Formation) and the Beaufort Group (Abrahamskraal Formation), which researchers Rubidge and Oelofsen considered to be a paleoshoreline. It was named by Rubudge in 1995 after the most common therapsid present in the area, the Eodicynodon oosthuizeni. The lower boundary is set by the first appearance of Eodicynodon oosthuizeni in the zone, and the upper boundary by the first appearance of Eosimops newtoni, a dicynodont. Laterally, the biozone runs from Laingsburg to the south of Rietbron. The zone is identified by the existence of Eodicynodon oosthuizeni, a dicynodont, along with Tapinocaninus pamelae and Australosyodon nyaphulii, two types of dinocephalians. Tapinocaninus fossils account for approximately 10% of all tetrapod fossils found in this biozone. The thickness of this biozone ranges from 320 to 1100m, with the maximum thickness occurring at the Prince Albert Road station, and gradually thinning to the east and west of this point. The biozone is made up of siltstones, sandstones, and mudstones. Fossils of tetrapods are rare in this area, however, there are copious impressions of equisetalian and Glossopteris stems and leaves on the mudrock surfaces. When found, therapsid fossils are typically well preserved in the mud rock strata, and dinocephalians found in fine-grained sandstone. ==References==
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