TL;DR: Examination of 35 skeletal characters in six living and nine extinct taxa suggest that there are four distinct clades in the Pelomedusidae (sensu lato).
Abstract: Thirteen new specimens in the collection of the American Museum of Natural History allow redescription of the lower Cretaceous side-necked turtle, Araripemys barretoi Price 1973. Araripemys is one of the three oldest pleurodires known for which the skeletal morphology can be completely described. The genus is incorporated into a phylogenetic analysis of pelomedusid (sensu lato) turtles. Examination of 35 skeletal characters in six living and nine extinct taxa suggest that there are four distinct clades in the Pelomedusidae (sensu lato). These are the Araripemydidae (including Araripemys and an undescribed genus from the same locality), the Pelomedusidae (restricted to the living genera Pelusios and Pelomedusa), the Bothremydidae (including at least five extinct genera) and the Podocnemidae (including the living genera Podocnemis, Peltocephalus and Erymnochelys, and a series of extinct genera). The hyperfamily name Pelomedusoides is available and accommodates these four families.
TL;DR: Using nearly range-wide sampling, mitochondrial DNA is analyzed and a minimum of 12 deeply divergent species-level clades are identified and six new Pelomedusa species are described, some of which can only be identified by molecular markers and are therefore morphologically cryptic taxa.
Abstract: Using nearly range-wide sampling, we analyze up to 1848 bp of mitochondrial DNA of 183 helmeted terrapins and identify a minimum of 12 deeply divergent species-level clades. Uncorrected p distances of these clades equal or clearly exceed those between the currently recognized species of Pelusios, the genus most closely related to Pelomedusa. We correlate genetic discontinuities of Pelomedusa with data on morphology and endoparasites and describe six new Pelomedusa species. Moreover, we restrict the name Pelomedusa subrufa (Bonnaterre, 1789) to one genetic lineage and resurrect three further species from its synonymy, namely P. galeata (Schoepff, 1792), P. gehafie (Ruppell, 1835), and P. olivacea (Schweigger, 1812). In addition to these ten Pelomedusa species, we identify two further clades from Cameroon and Sudan with similar levels of genetic divergence that remain unnamed candidate species. We also note that some problematical terrapins from South Africa and Somalia may represent two additional candidate species. Some of the Pelomedusa species are morphologically distinctive, whilst others can only be identified by molecular markers and are therefore morphologically cryptic taxa.
TL;DR: A future taxonomic revision should extend the geographical sampling of molecular data, specifically focusing on contact zones and the possible sympatric occurrence of lineages without admixture, and evaluate the morphology of the various genealogical lineages using the type specimens or topotypical material of the numerous junior synonyms of P. subrufa.
TL;DR: The distribution of fossils and the ecology of the living Pelusios suggest that most foraging for turtles took place in the shallow water of the marshy lake border, and there was either a change in the foraging technique from the earlier to later times represented in the deposits, or achange in the environment near the hominid occupational sites.
Abstract: Four species of fossil turtles are reported from Pleistocene deposits of Olduvai Gorge. Two are testudinids; one is identical to the extant Geochelone pardalis, and the other is a large undescribed species. The two remaining turtle species are pelomedusids. One is identical to the extant Pelusios sinuatus; the other is described as a new genus and species (Latisternon microsulcae) and, on the basis of shell morphology, is presumed to have been more terrestrial than extant pelomedusid species. Most of the fossil chelonian remains are believed to have been accumulated by foraging hominids. The Pelusios sinuatus fossils greatly outnumber those of the other three species; apparently it was the most assiduously hunted. The distribution of fossils and the ecology of the living Pelusios suggest that most foraging for turtles took place in the shallow water of the marshy lake border. There was either a change in the foraging technique from the earlier to later times represented in the deposits, or a change in the environment near the hominid occupational sites.
TL;DR: The genus Haemogregarina has a low host specificity crossing the family level of its vertebrate hosts and that its distribution is likely to be linked to the vector and definitive host – the leech.
Abstract: The majority of Haemogregarina species have been based on the morphology of their erythrocytic stages and supposed strict host specificity. The quantity of species with a limited number of overlapping diagnostic traits has led to a considerable mess in haemogregarine taxonomy and significant synonymy. We analysed host specificity, intra- and interspecific variability, evolutionary relationships, and the distribution of the type species of the genus Haemogregarina – H. stepanowi. The morphology of blood stages and 18S rDNA sequences of this haemogregarine from four western Palaearctic hard-shelled freshwater turtles (Emys orbicularis, Mauremys caspica, Mauremys leprosa and Mauremys rivulata) were compared with Haemogregarina balli. Additional sequences of 18S rDNA of Haemogregarina-like isolates collected from three species of African hinged terrapins (genus Pelusios) were used to enlarge the dataset for phylogenetic analyses. Thirteen sequences (1085 bp) of Haemogregarina representing all four western Palaearctic turtle species were identical, corresponding to H. stepanowi, which is closely related to the Nearctic species H. balli. In our analyses, Haemogregarina spp. constituted a monophyletic clade sister to the genus Hepatozoon. Haemogregarina stepanowi possesses a wide distribution range from the Maghreb, through Europe, Turkey and the Middle East to Iran. We consider that the genus Haemogregarina has a low host specificity crossing the family level of its vertebrate hosts and that its distribution is likely to be linked to the vector and definitive host – the leech.