Abstract
The only true living endothermic vertebrates are birds and mammals, which produce and regulate their internal temperature quite independently from their surroundings. For mammal ancestors, anatomical clues suggest that endothermy originated during the Permian or Triassic. Here we investigate the origin of mammalian thermoregulation by analysing apatite stable oxygen isotope compositions (δ18Op) of some of their Permo-Triassic therapsid relatives. Comparing of the δ18Op values of therapsid bone and tooth apatites to those of co-existing non-therapsid tetrapods, demonstrates different body temperatures and thermoregulatory strategies. It is proposed that cynodonts and dicynodonts independently acquired constant elevated thermometabolism, respectively within the Eucynodontia and Lystrosauridae + Kannemeyeriiformes clades. We conclude that mammalian endothermy originated in the Epicynodontia during the middle-late Permian. Major global climatic and environmental fluctuations were the most likely selective pressures on the success of such elevated thermometabolism.
Highlights
One key adaptation enabling tetrapods to cope with fluctuating climatic conditions was the acquisition of endothermy (Paaijmans et al, 2013)
Following the protocol of previous research undertaken to establish the Permo-Triassic climatic conditions that prevailed during which South African tetrapods, including therapsids, radiated (Rey et al, 2016), this study aims to investigate thermophysiological strategies developed by various Permo-Triassic therapsid groups using the stable oxygen isotope compositions of their phosphatic remains
The 13 sampled South African Permian therapsids come from three different assemblage zones (AZ) of the Beaufort Group: the lower Tapinocephalus AZ, the Tropidostoma AZ and the lower Daptocephalus AZ (Viglietti et al, 2016)
Summary
One key adaptation enabling tetrapods to cope with fluctuating climatic conditions was the acquisition of endothermy (Paaijmans et al, 2013). This character is defined here as the ability to actively produce body heat through metabolic activity (Cannon and Nedergaard, 2004). Its development and anchoring in populations constitutes a major step in vertebrate evolution because it modified the energy relationships between organisms and their environments. By actively raising and maintaining body temperature within a narrow range that allows optimal physiological and biochemical
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