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The origin of tympanic hearing in early synapsids is still controversial, because little is known about their inner ear and the function of their sound conducting apparatus. Here I describe the earliest known tympanic ear in the synapsid lineage, the ear of Pristerodon (Therapsida, Anomodontia) from the Late Permian of South Africa, which was virtually reconstructed from neutron tomographic data. Although Pristerodon is not a direct ancestor of mammals, its inner ear with distinctive cochlear cavity represents a connecting link between the primitive therapsid inner ear and the mammalian inner ear. The anatomy of the sound conducting apparatus of Pristerodon and the increased sound pressure transformer ratio points to a sensitivity to airborne sound. Furthermore, the origins of the cochlea and impedance matching hearing in synapsids coincided with the loss of contact between head and substrate, which already took place at least in Late Permian therapsids even before the postdentary bones became detached from the mandible.
I describe the anterior part of the externally poorly preserved skull of a therocephalian from the Karoo Basin in South Africa, using the method of serial grinding. The skull is incomplete, and its estimated length in life is 130 mm. The skull can be assigned to the Akidnognathidae with some confidence. The stratigraphic age of the specimen and its locality are not known, but the surrounding sediment suggests that it may be from the Upper Permian Dicynodon Assemblage Zone. It has five or six postcanine teeth, and a poorly developed crista choanalis. The sinuses and canals of the snout are recognized, and it is believed that the sinus positioned posteriorly in the snout (posterior maxillary sinus) is homologous with the maxillary sinus of anomodonts and cynodonts. It also shows similarities to the infraorbital canal of early mammals, such as Morganucodon. An anteriorly positioned sinus (anterior maxillary sinus), situated directly behind the canine root, is homologized with the maxillary sinus of gorgonopsians. In addition, I identify the previously undescribed canal (designated anterior maxillary canal), leading from the anterior maxillary sinus antero−dorsally. No evidence for maxilloturbinals was found in contrast to the condition known in the primitive therocephalian Glanosuchus
The affinities of the Early Permian synapsid Tetraceratops insignis have been reevaluated several times since the early 20th century, being considered as an eothyridid, a sphenacodontid, or a therapsid. This controversy continues into the 21st century, with recently raised doubts about the interpretation of Tetraceratops as the oldest known therapsid, a hypothesis supported by the only redescription of this fossil in the second half of the 20th century. Our study examines the arguments proposed to refute therapsid affinities, and concludes that Tetraceratops indeed is the sister−group of all other known therapsids. The most recently published phylogenetic data matrix that includes Tetraceratops fails to confirm its therapsid affinities. However, adding seven characters to that matrix leads to the conclusion that Tetraceratops is the basal−most and oldest therapsid. The recent suggestion of a Laurasian origin of therapsids appears poorly supported; too few data are available on the distribution of Permian synapsids to settle this question.
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The distant evolutionary ancestry of mammals is documented by a rich therapsid fossil record. While sphenacodontid synapsids are considered the sister−group of therapsids, the place of origin of therapsids is an enigma, largely because of a long standing morphological and temporal gap (Olson’s Gap) in their fossil record. We describe a new large predatory synapsid, Raranimus dashankouensis gen. et sp. nov., from the Middle Permian of Dashankou in China which has a unique combination of therapsid and sphenacodontid features. This specimen is of great significance asit is a basal therapsid which is the sister taxon to all other therapsids. The fact that it was found in association with Early Permian tetrapods (Anakamacops and Belebey) suggests that it is the oldest therapsid and provides the first evidence of therapsid−bearing rocks which cover Olson’s Gap. It further supports that therapsids may have had a Laurasian rather than Gondwanan origin.
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