Putative trackways

A set of footprints was found in the Teekloof Formation of the Beaufort Group by C.S. MacRae (1990), believing to have been made by either Aulacephalodon or the related Rhachiocephalus.^[4] Biostratigraphy placed the formation that contained the tracks within the Cistecephalus Assemblage Zone.^[4] Two sets of tracks were found, most likely belonging to two different individuals, with a pace approximately 600–650 mm in length.^[4] The organism that made the tracks was a large, and heavily padded, homopodus quadruped with a short tail.^[4] The tracks had a width of 800 mm, which when combined with the short stride length suggests Aulacephalodon, or Rhachiocephalus, was an inefficient walker.^[4]

An additional set of trackways was found at the Asante Sana game preserve near Petersburg in the Balfour Formation of the Beaufort Group. The morphology of the manus tracks, referred to the ichnospecies Dicynodontipus icelsi, compares well with the manus of Aulacephalodon.^[5]

Origins of Aulacephalodon

Controversy over the number of species belonging to the genus Aulacephalodon has existed since the first specimens were discovered. The majority of specimens found were fragments, making proper diagnosis difficult for many of the specimens. Owen (1844) first described members of this genus as Dicynodon bainii, with five more species of dicynodont being discovered in subsequent years. Seeley (1898) divided Dicynodon into two subgenera and created the subgenus Aulacephalodon, suggesting all dicynodonts with a short snout and wide skull should be included in the subgenus. Two additional dicynodont species were discovered by Broom in 1912 and 1913. Broom (1921) also proposed a new subgenus of Dicynodon, Bainia, to describe tusked members of Dicynodon. When Broom finally recognized Seeley's subgenus, Aulacephalodon, as a valid genus in 1932. However, the spelling was altered to Aulacocephalodon. The incorrect genus Aulacocephalodon was used for many years until the correct spelling was pointed out by Keyser (1969). At least 17 species have been described as members of Aulacephalodon, however it is noted many of the features used to distinguish between the different species are size-dependent and highly susceptible to distortion. This has resulted in Aulacephalodon bainii being recognized as the type species of the genus, with the previous 17 species described as synonymous members of the species at various stages of growth.^[3]

Aulacephalodon bainii and Aulacephalodon peavoti

When Aulacephalodon peavoti was first described, the cranium of one specimen was compared to Aulacephalodon bainii to determine if A. peavoti can accurately be described as Aulacephalodon. The most distinct difference between A. bainii and A. peavoti is that specimens of A. peavoti are not found to possess tusks, which is a notable feature of A. bainii and Aulacephalodon. A. peavoti is also found to have a wider and more upright scapula blade compared to A. bainii, with deeper fossa on the proximal end of the scapula. While both species share some similar post-cranial features, there are numerous differences in the shapes of various girdle and forelimb elements prevents paleontologists from definitively recognizing A. peavoti as a member of Aulacephalodon.^[1]

Diet

Aulacephalodon skulls show the transverse anterior tip of their short snout is reinforced by the palatal ridges and ridges on the snout, resulting in biting action restricted to the tip of their jaws.^[3] The restricted jaw motion and presence of a horny beak structure suggests that Aulacephalodon were herbivores.^[3] Based on the arid climate of the Cistecephalus Zone, Aulacephalodon is thought to have fed on the stems of woody plants present in the region.^[6] The most commonly occurring plants in the region, Schizoneura and Phyllotheca, would have been available to Aulacephalodon to feed on.^[3] Tollman et al. (1980) suggests that as a function of their ontogenetically increasing size, the breadth of their occupied niche increased throughout their life that resulted in changes to the size and type of food Aulacephalodon obtained.^[3] A similar phenomenon is observed in modern genera Alligator and Crocodylus.^[3]

Compared to the related Oudenodon and Rhachiocephalus, Aulacephalodon bore differently-specialized biting mechanisms; Aulacephalodon has been hypothesized to have bit using the anterior tips of the jaws, while Oudenodon and Rhachiocephalus bit using the sides of the beak.^[7]

Sexual dimorphism

Skull of Aulacephalodon bainii

Tollman et al. (1980) suggests that the nasal bosses in the skulls of collected Aulacephalodon specimens provide the most compelling evidence of sexual dimorphism in Aulacephalodon fossils.^[3] Morphological studies found that the sizes of the nasal bosses of collected specimens can be categorized into three different size ranges, with specimens possessing the largest sized nasal bosses assumed to be mature males.^[3] Female Aulacephalodon were found to be specimens with weakly developed nasal bosses.^[3] Specimens that were thought to represent mature males also had larger craniums with a thicker squamosal at the border of the zygomatic arch.^[3] Female specimens showed no thickening in the zygomatic arch.^[3] The canine tusks also appear to be longer and further apart in male specimens.^[3] Tollman et al. suggests sexual dimorphism existed in Aulacephalodon as a means of sexual selection and as a display mechanism.^[3] Important limitations to this analysis are that no specimen showed entirely male or female characters and many of the specimens used were characterized as immature juveniles.^[3] Possible explanations for this observation are that non-dimorphic characters present in the crania effectively mask the sexual dimorphism characters, or sexual dimorphic characters were not present in the fossils due to a lack of measurable characters.^[3]

Possible explanation for extinction

Some paleontologists suggest that the end-Permian tetrapod extinctions, including Aulacephalodon, may have been caused by lowered atmospheric oxygen concentrations, resulting in both environmental and organismal hypoxia. The increase in size of the internal nares and secondary palate would decrease the respiratory efficiency of large anomodont therapsids, such as Aulacephalodon. Comparison of Triassic and late-Permian therapsids shows an increase in separation between the buccal and nasal cavities and larger internal nares in Triassic therapsids, demonstrating an increased efficiency of oxygen transport in a lower-oxygen environment. An important caveat to this explanation for extinction is that hypoxia is most likely one of many compounding environmental factors that led to the end-Permian tetrapod extinction.^[11]