Abstract

Using two mitochondrial DNA fragments and 13 microsatellite loci, we examined the phylogeographic structure and taxonomy of two codistributed snake species (Natrix natrix,N. tessellata) in their eastern distribution area, with a focus on Turkey. We found evidence for frequent interspecific hybridization, previously thought to be extremely rare, and for backcrosses. This underscores that closely related sympatric species should be studied together because otherwise the signal of hybridization will be missed. Furthermore, the phylogeographic patterns of the two species show many parallels, suggestive of a shared biogeographic history. In general, the phylogeographies follow the paradigm of southern richness to northern purity, but the dice snake has some additional lineages in the south and east in regions where grass snakes do not occur. For both species, the Balkan Peninsula and the Caucasus region served as glacial refugia, with several mitochondrial lineages occurring in close proximity. Our results show that the mitochondrial divergences in both species match nuclear genomic differentiation. Yet, in the former glacial refugia of grass snakes there are fewer nuclear clusters than mitochondrial lineages, suggesting that Holocene range expansions transformed the glacial hotspots in melting pots where only the mitochondrial lineages persisted, bearing witness of former diversity. On the other hand, the deep mitochondrial divergences inN. tessellataacross its entire range indicate that more than one species could be involved, even though lacking microsatellite data outside of Turkey prevent firm conclusions. On the contrary, our microsatellite and mitochondrial data corroborate thatN. megalocephalais invalid and not differentiated from sympatric populations ofN. natrix. For Cypriot grass snakes, our analyses yielded conflicting results. A critical assessment of the available evidence suggests thatN. natrixis a genetically impoverished recent invader on Cyprus and taxonomically not distinct from a subspecies also occurring in western Anatolia and the southern Balkans. Based on combined mitochondrial and nuclear genomic evidence we propose that for grass snakes the following subspecies should be recognized in our study region: (1)Natrix natrix vulgarisLaurenti, 1768, southeastern Central Europe and northern Balkans; (2)Natrix natrix moreotica(Bedriaga, 1882), southern Balkans, western Anatolia, and Cyprus; and (3)Natrix natrix scutata(Pallas, 1771), eastern Anatolia, Caucasus region, Iran, northeastern distribution range (from eastern Poland and Finland to Kazakhstan and the Lake Baikal region). Thus,Natrix natrix cypriaca(Hecht, 1930) becomes a junior synonym ofN. n. moreoticaandNatrix natrix persa(Pallas, 1814) becomes a junior synonym ofN. n. scutata. Due to insufficient material, we could not resolve the status ofNatrix natrix syriaca(Hecht, 1930) from the Gulf of İskenderun, southeastern Turkey.

Highlights

  • The genus Natrix Laurenti, 1768 comprises five widely distributed Palearctic snake species (Speybroeck et al 2020)

  • In parsimony network analyses, each mitochondrial lineage of Natrix natrix and N. tessellata revealed by phylogenetic analyses (Guicking et al 2009; Guicking and Joger 2011; Kindler et al 2013) corresponded to a distinct haplotype cluster

  • Acknowledging that Cypriot grass snakes are distinct on the nuclear genomic level only due to genetic impoverishment, we propose that Cypriot populations should be taxonomically lumped together with grass snakes from the southern Balkans and western Anatolia characterized by mitochondrial DNA (mtDNA) lineage 7

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Summary

Introduction

The genus Natrix Laurenti, 1768 comprises five widely distributed Palearctic snake species (Speybroeck et al 2020). The viperine snake Natrix maura (Linnaeus, 1758) and the dice snake Natrix tessellata (Laurenti, 1768) are true water snakes (Gruschwitz et al 1999; Schätti 1999) and have been regarded as distinct species since their description in the mid-18th century. Natrix tessellata occurs across most of mainland Italy and ranges from the Czech Republic and southern and eastern Austria eastward through the south of Eastern Europe to northwestern China (Xinjiang); a few isolated Central European populations (Germany, Switzerland) are witness of a formerly wider Holocene distribution in the northwest. While the ranges of N. maura and N. tessellata are largely mutually exclusive and only overlap in northwestern Italy, these two water snakes occur in wide sympatry with the three grass snake species (N. astreptophora, N. helvetica, N. natrix sensu stricto)

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