Eunotosaurus

Eunotosaurus was named in 1892 based on a specimen (now NHMUK PV R 1968 in the Natural History Museum, London) that he had obtained from Mr. L. Pienaar at the farm Weltevreden near Beaufort West, during Seeley's visit to South Africa in 1889. Seeley was uncertain of the systematic position of Eunotosaurus, but postulated that it was likely referable to the Mesosauria, based on the pubis anatomy. It was not until 1914 that it was proposed to be an ancestor of Chelonia, the turtle order. English zoologist D. M. S. Watson claimed that Eunotosaurus was transitional between cotylosaurs (now referred to as captorhinids) and Chelonia. He compared it to "Archichelone", a name he devised for a hypothetical chelonian ancestor, noting that its ribs appeared to be intermediate between those of turtles and other tetrapods. Watson's "Archichelone" had a pelvic girdle that was pushed back on the vertebral column and placed under the shell. However, fossils of Eunotosaurus show that the pelvis is in the normal tetrapod position and is placed over the ribs rather than within them, as in modern turtles. Many fossils have been found showing a semi-rigid, turtle-like rib cage, one which presumably necessitated a tortoise-like fashion of walking. Eunotosaurus was considered the ancestor of turtles until the late 1940s. In his 1956 book Osteology of the Reptiles, American paleontologist Alfred Sherwood Romer claimed that Eunotosaurus could not be included within Chelonia based on the available evidence. He placed it within Anapsida in its own order incertae sedis. Over a century after its naming, Eunotosaurus was known from less than a dozen specimens, with very little material known from the skull. Despite the paucity of material, it was well described. Two additional skeletons were unearthed from the Karoo Supergroup and described in 1999. They are now housed in the Bernard Price Institute for Palaeontological Research in Johannesburg and the National Museum, Bloemfontein. While relatively rare, Eunotosaurus is common enough in the Karoo to be used as a biostratigraphic marker. It is present in the upper Tapinocephalus Assemblage Zone and in all parts of the succeeding Lycosuchus - Eunotosaurus Subzone of the Endothiodon Assemblage Zone. In 2024, an articulated Eunotosaurus fossil was described from the collections of the Cultural & Museum Centre Karonga in Malawi, having been discovered in 2016 by a herdsman in the Mwesia Beds of Karonga. This marked the first occurrence of Eunotosaurus outside South Africa, and confirmed that the Mwesia Beds correspond to the Tapinocephalus and Pristerognathus zones. ==Description==

Eunotosaurus reached up to in total body length. Histological analysis of cross-sections of the ribs indicates that they grew in three different phases as an individual developed. As is the case in most land vertebrates, the first phase involves the growth of a rib primordium that ossifies into a rib bone. The second phase, which deviates from most other land vertebrates, is the development of a shelf of bone above the main shaft of the rib to form the T-shape. The third and final phase is the widening of the lower ridge into a teardrop-like shape, reinforcing the rib. While the third phase is unique to Eunotosaurus, the second phase is also seen in modern turtles. In turtles, the shelf of bone that forms from the rib shaft becomes a plate of the shell or carapace. In each rib of Eunotosaurus, the posterior surface of the lower ridge has Sharpey's fibers embedded in it. Sharpey's fibers help anchor muscles to bone. Most amniotes have Sharpey's fibers on the posterior and anterior edges of the ribs because the ribs are connected to each other by intercostal muscles, which are muscles that assist in breathing. The lack of Sharpey's fibers on the anterior side of the ribs of Eunotosaurus suggests that it lacked functional intercostal muscles. Turtles also lack intercostal muscles and instead have muscles that connect to the undersides of the ribs for the purpose of locomotion. If Eunotosaurus is close to the ancestry of turtles, it may have had similar sets of muscles. ==Classification==

The ribs of Eunotosaurus are very wide and flat, touching each other to form broad plates similar to the carapace of turtles. Moreover, the number of vertebrae, the size of the vertebrae, and their structure are nearly identical to those of some turtles. Despite its many similarities to turtles, Eunotosaurus has a skull that shares many characteristics with the skulls of more ancestral reptiles, resulting in many studies placing it in the extinct group Parareptilia. Phylogenetic analyses that use only the physical features of fossils and living species to determine evolutionary relationships have often shown strong support for both Eunotosaurus and turtles being descendants of parareptiles. However, analyses which also include genetic data from living reptiles strongly support the idea that turtles fall within a group called Diapsida, as close relatives of either lizards (in which case they would be lepidosauromorphs) or birds and crocodiles (making them archosauromorphs). According to this view, the expanded ribs and similar vertebral columns of Eunotosaurus and turtles may be a case of evolutionary convergence. However, the discovery of Pappochelys, a prehistoric species whose fossil remains show a mixture of features found in Eunotosaurus and the toothed stem-turtle Odontochelys, was suggested to resolve the issue. Though an analysis which included data from Pappochelys found weak support for the idea that Eunotosaurus was a parareptile, it found stronger support for the hypothesis that Eunotosaurus was itself a diapsid closely related to turtles, and that its apparently primitive, anapsid skull was probably developed as part of the turtle lineage, independently of parareptiles. In 1969, it was placed in the parareptile suborder Captorhinomorpha. In 2000, Eunotosaurus was placed in the clade Parareptilia, separate from turtles and cotylosaurs. A 2008 phylogenetic analysis of parareptiles found Eunotosaurus to be the sister taxon of Milleretta and thus within the family Millerettidae. Eunotosaurus was incorporated in a 2010 phylogenetic analysis that sought to determine the origin of turtles. }} The cladogram below follows the most likely result found by another analysis of turtle relationships, published by Rainer Schoch and Hans-Dieter Sues in 2015. This study found Eunotosaurus to be an actual early stem-turtle, though other versions of the analysis found weak support for it as a parareptile. of the inner ear The following cladogram is adapted from a 2022 study by Simões et al. Here, Eunotosaurus was recovered as neither a parareptile nor a stem-turtle, but as a basal neodiapsid located outside the reptilian crown group. }} In 2026, Evers and colleagues described the inner ear and semicircular canal anatomy of BP/1/7852, a Eunotosaurus specimen discovered ten years prior. Using high-resolution CT scans of the specimen, they identified features of the labyrinth in Eunotosaurus that are seen in both turtle-line reptiles and more ancestral neodiapsids outside of the reptile crown group. ==References==