Speciation typically involves a stage in which species can still exchange genetic material. Interspecific gene flow is facilitated by the hybrid zones that such species establish upon secondary contact. If one member of a hybridizing species pair displaces the other, their hybrid zone would move across the landscape. Although theory predicts that moving hybrid zones quickly stagnate, hybrid zones tracked over one or a few decades do not always follow such a limitation. This suggests that hybrid zones have the potential to traverse considerable distances over extended periods of time. When hybrid zones move, introgression is predicted to result in biased gene flow of selectively neutral alleles, from the receding species into the advancing species. We test for such a genomic footprint of hybrid zone movement in a pair of crested newt species (genus Triturus) for which we have a priori support for westward hybrid zone movement. We perform a multilocus phylogeographical survey and conduct Bayesian clustering analysis, estimation of ancestry and heterozygosity, and geographical cline analysis. In a 600 km wide area east of the present day hybrid zone a genomic footprint constitutes empirical evidence consistent with westward hybrid zone movement. The crested newt case suggests that hybrid zone movement can occur over an extensive span of time and space. Inferring hybrid zone movement provides fundamental insight into historical biogeography and the speciation process, and we anticipate that hybrid zones will prove to be far more mobile than currently appreciated.
Two and perhaps three taxa of Lissotriton newt occur in Turkey. Their species status is controversial. The distribution of these taxa and the taxonomic status of each are reviewed and discussed. A database of 128 Turkish Lissotriton localities was compiled and species distribution models were constructed. We reiterate that the presence of Lissotriton (vulgaris) lantzi in Turkey is disputed and needs confirmation. The range of Lissotriton (vulgaris) kosswigi is restricted to north-western Anatolia – given the small global range of this Turkey endemic, a closer look at its conservation status is warranted. The distribution of Lissotriton
vulgaris
schmidtleri covers western Asiatic and European Turkey. The findings support an allopatric distribution of the Turkish Lissotriton species. We reflect on the biological significance of previously reported morphological intermediates between Lissotriton (vulgaris) kosswigi and Lissotriton
vulgaris
schmidtleri in the light of the recent proposal to recognize kosswigi at the species level. The available data are in line with species status for Lissotriton (vulgaris) lantzi and Lissotriton (vulgaris) kosswigi. Although Lissotriton
vulgaris
schmidtleri is a genetically diverged taxon as well, the extent of gene flow with parapatric European Lissotriton taxa is as yet unknown.
Patara Beach is one of the most important nesting beaches in Turkey for Caretta caretta. In this paper, we provide information on the nesting activity, spatial and temporal distribution of nesting, nesting and hatching success, nesting density, incubation duration, clutch size, and predation ratio of sea turtles over four nesting periods, namely 2010, 2012, 2013, and 2014. An average of 179.75 nests were recorded per year, and the overall nesting density was 15.50 nests/km while 68.20 loggerhead sea turtle eggs were recorded per nest. The hatching success was 44.05% from these counted eggs and 38.04% of hatchlings were able to reach the sea. We also observed 3 Chelonia mydas nests. The highest nesting activity during our monitoring over the past 20 years was obtained in 2013. The average annual number of turtle nests in Patara over 20 nesting seasons was 94.70.
IntroductionLycian salamanders of the genus Lyciasalamandra were first described by Steindachner (1891) from Dodurga (Muğla, Turkey) as Molge luschani. Wolterstorff (1925) then classified the Lycian salamanders together with the Caucasian salamanders in the genus Mertensiella. Nine subspecies of M. luschani have been described, accepting the Dodurga specimens as the nominate race (
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