Malayemys

Abstract: Based on an integrative taxonomic approach, we examine the differentiation of Southeast Asian snail-eating turtles using information from 1863 bp of mitochondrial DNA, 12 microsatellite loci, morphology and a correlative species distribution model. Our analyses reveal three genetically distinct groups with limited mitochondrial introgression in one group. All three groups exhibit distinct nuclear gene pools and distinct morphology. Two of these groups correspond to the previously recognized species Malayemys macrocephala (Chao Phraya Basin) and M. subtrijuga (Lower Mekong Basin). The third and genetically most divergent group from the Khorat Basin represents a previously unrecognized species, which is described herein. Although Malayemys are extensively traded and used for religious release, only few studied turtles appear to be translocated by humans. Historic fluctuations in potential distributions were assessed using species distribution models (SDMs). The Last Glacial Maximum (LGM) projection of the predictive SDMs suggests two distinct glacial distribution ranges, implying that the divergence of M. macrocephala and M. subtrijuga occurred in allopatry and was triggered by Pleistocene climate fluctuations. Only the projection derived from the global circulation model MIROC reveals a distinct third glacial distribution range for the newly discovered Malayemys species.

Abstract: (with eight text-figures) ABSTRACT.- Geographic variation was studied in the south-east Asian turtles of the genus Malayemys (Testudines: Bataguridae). Discriminant function analysis of head-stripe and shell characters reveals a clear pattern of geographic variation that is consistent with the topography of south-east Asia and the poor dispersal abilities of these turtles. Two phenotypically and morphologically distinct groups of Malayemys occur allopatrically in lowland areas of mainland south-east Asia, and my data concludes that each should be recognized as a distinct species. Turtles from the Mekong River Basin retain the name Malayemys subtrijuga (Schlegel and Muller, 1844), whereas those from the Chao Phraya and Mae Klong river basins, coastal areas of south-eastern Thailand, and the Malay Peninsula are assigned the name Malayemys macrocephala (Gray, 1859). Malayemys macrocephala has four or fewer nasal stripes (99%) and an infraorbital stripe that is relatively wide at the loreal seam (98% of InfSW/HW=0.07-0.18) and does not extend or extends only slightly superior to the loreal seam (96%). Conversely, M. subtrijuga has six or more nasal stripes (89%) and an infraorbital stripe that is relatively narrow at the loreal seam (92% of InfSW/HW=0.02-0.06), extends completely superior to the loreal seam (96%), and usually joins the supraorbital stripe (64%). Female M. macrocephala also have relatively longer AnL and relatively shorter Vert5L and PecL than M. subtrijuga. Similarly, male M. macrocephala have relatively longer PPLL and AbdL, relatively shorter Pleu1L and PecL, and greater RLatK values than M. subtrijuga. Both species are potentially threatened by overcollection and habitat destruction, and should be protected as separate taxa of concern. In addition, discriminant function analysis of shell and head-stripe characters suggests that M. subtrijuga on Java are derived by human intervention primarily from the Mekong River Basin.

Abstract: The present study examined karyotypes of 16 genera and, along with previous reports, chromosomal data are now available for 18 of the 23 recognized batagurine genera. There are no karyotypic data available for the members of McDowell's (1964) Hardella complex. The Batagur, Heosemys and Geoemyda complexes retain the hypothesized primitive karyotype for the subfamily (2n=52). All the genera in these three complexes have been examined except Batagur and Annamemys. The Orlitia complex is karyotypically distinct with 2n=50 and the NOR located terminally on a large microchromosome. The genus Malayemys inclusion in the Batagur complex is not supported. Malayemys is characterized by a 2n=50 karyotype, with the NOR located interstitially on a large microchromosome. The Malayemys complex is erected to contain this genus at a point intermediate between the Orlitia complex and the subfamily Emydinae. Malayemys and the emydines are karyotypically indistinguishable. The Neotropical genus Rhinoclemmys (Geoemyda complex) differs only slightly from the primitive batagurine karyotype in the position of the NOR. The species R. funerea and R. punctularia further differ in possessing one less metacentric macrochomosome. An interesting situation involves two subspecies of R. punctularia. The nominate subspecies is characterized by a 2n=56 karyotype, while R. p. melanosterna reportedly has a 2n=52 karyotype. Such a difference is interpreted as indicative of genetic differentiation between the two forms of a magnitude inconsistent with considering them as conspecific. Taken together with zoogeographic considerations, the karyotypic difference between the forms R. p. punctularia and R. p. melanosterna seem sufficient to warrant species distinction for R. melanosterna as previously suggested by Pritchard (1979b).

Abstract: The Siamese shield leech Placobdelloides siamensis (Oka, 1917) Sawyer, 1986 (Euhirudinea: Glossiphoniidae) was collected from five new host species, Southeastern Asian Box Turtle (Cuora amboinensis ), Yellow-headed Temple Turtle (Heosemys annandalii ), Malayan Snail-eating Turtle (Malayemys macrocephala ), Mekong Snail-eating Turtle (M. subtrijuga ), and Khorat Snail-eating Turtle (M. khoratensis ) and was found for the first time in Udon Thani, Thailand. Examination of live leeches provided, for the first time, data on coloration and the combination of parental care behavior, both carrying cocoons and attaching cocoons to the substrate. This species was separated from its congeners based on the following characters: one pair of eyes; spines at proboscis subterminal; mouth terminal on oral sucker; absent plaque in neck region; gonopores located in furrow and separated by two annuli; distinctly triannulated mid-body segments; crop with seven pairs and branched caeca; caudal sucker slightly over half of maximum body width; and strongly dorsal papillae. Phylogenetic relationships based on the COI and ND1 genes were clarified and demonstrated that the species is distinct from others. The original description was amended and the taxonomic history is discussed.