Probable hair in a therapsid coprolite from the Permian of Russia (photo by K. Owocki; see Bajdek et al., 2015)
Ectothermic or endothermic
An obvious difference between modern reptiles and mammals is that the former are ectotherms and the latter endotherms: whereas the body temperature of reptiles is dependent on the prevailing environmental temperatures, it is regulated to remain nearly constant in mammals. We can also note that: (1) mammals have fur and reptiles do not, and (2) reptiles are characterized by a much longer digestion (slower metabolism) than mammals of a comparable body mass. As a consequence, many modern reptiles have a “lower-energy” lifestyle than mammals.
It becomes less obvious when we go back in time… Mammals evolved in the Triassic Period, and questions paleontologists ask themselves are: when did the endothermy in their evolutionary lineage appear? Were already the late Palaeozoic and early Mesozoic ancestors of mammals (called therapsids or mammal-like reptiles) endothermic?
In the 1970s, the American paleontologist Robert T. Bakker published innovative ideas on the physiology of mammal-like reptiles (and dinosaurs). He hypothesized that therapsids had fur and provided several lines of evidence that they were endotherms: (1) Therapsid bones lacked growth rings and had closely packed blood vessels and Haversian canals. (2) Some of them were distributed in cold temperate zones. (3) Short, stocky body proportions in many therapsids might have been a device to conserve heat. (4) Their predator–prey ratios, which depend on the energetic requirements of the predators, were lower than those of ectotherms.
R.T. Bakker’s ideas on the physiology of therapsids (and dinosaurs) have been accepted by most paleontologists and are well-known to the public. Nevertheless, because many of them are rather indirect lines of evidence, we now seek for new clues. Coprolites, i.e. fossil feces, being metabolistic byproducts provide such new and valuable data on the metabolism of their producers. In fact, the study of coprolites has during the last couple of years shed new light on the physiology of mammalian ancestors. For example, it was argued in the article on coprolites of a giant dicynodont from the Triassic of Poland, that these herbivorous and toothless therapsids had a rather slow metabolism.
Furthermore, in 2015, another piece of the puzzle of mammalian endothermy was added when our team composed of seven researchers from Poland, Sweden, and Russia (P. Bajdek, M. Qvarnström, K. Owocki, T. Sulej, A.G. Sennikov, V.K. Golubev, and G. Niedźwiedzki) published a new paper on coprolites. The coprolites we studied were produced by Late Permian carnivorous therapsids, over 252 million years ago, and excavated during a Polish–Russian expedition to the Vyazniki site, European Russia.
Undigested bones and the fast metabolism
The Vyazniki site has yielded various morphotypes of coprolites (which will soon be discussed again on the blog). Our paper from 2015 focuses on only two big coprolite morphotypes: A and B. Whereas undigested bone fragments are present in the type-A coprolites, they are quite rare and highly degraded in the type-B coprolites. As said above, reptiles are characterized by a much longer digestion than mammals, and, for example, crocodiles practically completely digest the bones they ingest. On the contrary, undigested bones are commonly found in the feces of mammals. Following these arguments, the bone-rich coprolites of type A would have interestingly been produced by some kind animals of a fast metabolism.
As such, the team of Krzysztof Owocki ascribed, in 2012, the bone-rich type-A coprolites to therapsid carnivores and the bone-barren type-B coprolites to archosauromorphs or other non-therapsid carnivores. Both therapsids and archosauromorphs are known from the fossil record of Vyazniki, but therapsids would have been more expected to have a fast metabolism than early archosauromorphs (ancestors of modern crocodiles and birds). This interpretation is supported by finds from the Upper Permian of South Africa. Already in 2011, the paleobiological context allowed Roger M.H. Smith and Jennifer Botha-Brink to link several bone-rich coprolite morphotypes from the Upper Permian of South Africa to carnivorous therapsids.
The oldest hairs
The researchers from South Africa have found more than just bones in the Permian coprolites. Some coprolites contain enigmatic elongated structures, that are on average 14 μm in diameter and reaching up to 5 mm in length. Roger M.H. Smith and Jennifer Botha-Brink suggested that these structures were remains of plants, fungi or, perhaps, hairs. It was exciting to our team to find comparable structures in a therapsid coprolite from the Upper Permian of Vyazniki, Russia. By the use of light and scanning electron microscopes we studied them in great detail, including their geochemistry. The structures we described from Russia are ten time larger in diameter than those from South Africa, and the largest one is over 5 mm long. They are interpreted as molds of hair-like elements; some even appear to show bifurcated hair roots! Hairs are well-resistant to digestion and often found in feces of modern carnivores.
If this interpretation is correct, these hairs are two times older than the previously earliest record of known hairs from Jurassic-Cretaceous mammals and imply that some therapsids had acquired insulation by the latest Paleozoic, prior to the rise of mammals. Hairs would probably have had a thermoregulatory function, as an insulation. Some researchers have also suggested that hairs could be tactile in origin. In 1968, G.H. Findlay hypothesized that perforations present in a skull of the Late Permian therapsid Olivera parringtoni reveal the presence of tactile hairs. Such hairs could have been of great use especially if mammals are descended from nocturnal reptiles. Hairs would make up for poor vision and moreover allow to conserve heat at night.
The discoveries from South Africa and Russia suggest that Late Permian therapsid carnivores had developed (1) an insulation (fur) and (2) an accelerated metabolism. Taken together, these features make us suspect that the late Paleozoic ancestors of mammals were already endotherms.
1 Częstochowa, Poland
2 Uppsala University, Sweden
Bajdek, P., Owocki, K., Niedźwiedzki, G., 2014. Putative dicynodont coprolites from the Upper Triassic of Poland. Palaeogeogr. Palaeoclimatol. Palaeoecol. 411, 1–17. doi: 10.1016/j.palaeo.2014.06.013
Bajdek, P., Qvarnström, M., Owocki, K., Sulej, T., Sennikov, A. G., Golubev, V. K., Niedźwiedzki, G., 2015. Microbiota and food residues including possible evidence of pre-mammalian hair in Upper Permian coprolites from Russia. Lethaia. doi: 10.1111/let.12156
Bakker, R.T., 1971. Dinosaur physiology and the origin of mammals. Evolution 25, 636–658.
Bakker, R.T., 1975. Dinosaur renaissance. Scientific American 232, 58–78.
Findlay, G.H., 1968. On the scaloposaurid skull of Oliviera parringtoni, Brink with a note on the origin of hair. Palaeontologia Africana 11, 47–59.
Owocki, K., Niedźwiedzki, G., Sennikov, A.G., Golubev, V.K., Janiszewska, K., Sulej, T., 2012. Upper Permian vertebrate coprolites from Vyazniki and Gorokhovets, Vyatkian regional stage, Russian Platform. Palaios 27, 867–877. doi: palo.2012.p12-017r
Smith, R.M.H., Botha-Brink, J., 2011. Morphology and composition of bone-bearing coprolites from the Late Permian Beaufort Group, Karoo Basin, South Africa. Palaeogeogr. Palaeoclimatol. Palaeoecol. 312, 40–53. doi: 10.1016/j.palaeo.2011.09.006