Being a dicynodont, Lystrosaurus had only two teeth, a pair of tusk-like canines, and is thought to have had a horny beak that was used for biting off pieces of vegetation. Lystrosaurus was a heavily built, herbivorous animal, approximately the size of a pig. The structure of its shoulders and hip joints suggest that Lystrosaurus moved with a semi-sprawling gait. The forelimbs were even more robust than the hindlimbs, and the animal is thought to have been a powerful digger that nested in burrows.
Lystrosaurus was by far the most common terrestrial vertebrate of the Early Triassic, accounting for as many as 95% of the total individuals in some fossil beds. It has often been suggested that it had anatomical features that enabled it to adapt better than most animals to the atmospheric conditions that were created by the Permian–Triassic extinction event and which persisted through the Early Triassic—low concentrations of oxygen and high concentrations of carbon dioxide. However, recent research suggests that these features were no more pronounced in Lystrosaurus than in genera that perished in the extinction or in genera that survived but were much less abundant than Lystrosaurus.
Lystrosaurus was a dicynodont therapsid, typically about 3 feet (0.9 m) long and weighing about 100 to 200 pounds (50 to 90 kg). One specimen unearthed in Karoo measured 2.5 meters long. Unlike other therapsids, dicynodonts had very short snouts and no teeth except for the tusk-like upper canines. Dicynodonts are generally thought to have had horny beaks like those of turtles, for shearing off pieces of vegetation which were then ground on a horny secondary palate when the mouth was closed. The jaw joint was weak and moved backwards and forwards with a shearing action, instead of the more common sideways or up and down movements. It is thought that the jaw muscles were attached unusually far forward on the skull and took up a lot of space on the top and back of the skull. As a result the eyes were set high and well forward on the skull, and the face was short.
Features of the skeleton indicate that Lystrosaurus moved with a semi-sprawling gait. The lower rear corner of the scapula (shoulder blade) was strongly ossified (built of strong bone), which suggests that movement of the scapula contributed to the stride length of the forelimbs and reduced the sideways flexing of the body. The five sacral vertebrae were massive but not fused to each other and to the pelvis, making the back more rigid and reducing sideways flexing while the animal was walking. Therapsids with fewer than five sacral vertebrae are thought to have had sprawling limbs, like those of modern lizards. In dinosaurs and mammals, which have erect limbs, the sacral vertebrae are fused to each other and to the pelvis. A buttress above each acetabulum (hip socket) is thought to have prevented dislocation of the femur (thigh bone) while Lystrosaurus was walking with a semi-sprawling gait. The forelimbs of Lystrosaurus were massive, and Lystrosaurus is thought to have been a powerful burrower.
Distribution and speciesEdit
Lystrosaurus fossils have been found in many Late Permian and Triassic terrestrial bone beds, most abundantly in Africa, and to a lesser extent in parts of what are now India, China, Mongolia, European Russia, and Antarctica (which was not over the South Pole at the time).
Species found in AfricaEdit
Most Lystrosaurus fossils have been found in the Balfour and Katberg Formations of the Karoo basin in South Africa; these specimens offer the best prospects of identifying species because they are the most numerous and have been studied for the longest time. As so often with fossils, there is debate in the paleontological community as to exactly how many species have been found in the Karoo. Studies from the 1930s to 1970s suggested a large number (23 in one case). However, by the 1980s and 1990s, only six species were recognized in the Karoo: L. curvatus, L. platyceps, L. oviceps, L. maccaigi, L. murrayi, and L. declivis. A study in 2011 reduced that number to four, treating the fossils previously labeled as L. platyceps and L. oviceps as members of L. curvatus.
L. maccaigi is the largest and apparently most specialized species, while L. curvatus was the least specialized. A Lystrosaurus-like fossil, Kwazulusaurus shakai, has also been found in South Africa. Although not assigned to the same genus, K. shakai is very similar to L. curvatus. Some paleontologists have therefore proposed that K. shakai was possibly an ancestor of or closely related to the ancestors of L. curvatus, while L. maccaigi arose from a different lineage. L. maccaigi is found only in sediments from the Permian period, and apparently did not survive the Permian–Triassic extinction event. Its specialized features and sudden appearance in the fossil record without an obvious ancestor may indicate that it immigrated into the Karoo from an area in which Late Permian sediments have not been found.
L. curvatus is found in a relatively narrow band of sediments from shortly before and after the extinction, and can be used as an approximate marker for the boundary between the Permian and Triassic periods. A skull identified as L. curvatus has been found in late Permian sediments from Zambia. For many years it had been thought that there were no Permian specimens of L. curvatus in the Karoo, which led to suggestions that L. curvatus immigrated from Zambia into the Karoo. However, a re-examination of Permian specimens in the Karoo has identified some as L. curvatus, and there is no need to assume immigration.
L. murrayi and L. declivis are found only in Triassic sediments.
Lystrosaurus georgi fossils have been found in the Earliest Triassic sediments of the Moscow Basin in Russia. It was probably closely related to the African Lystrosaurus curvatus, which is regarded as one of the least specialized species and has been found in very Late Permian and very Early Triassic sediments.