The narrow-headed vole, collared lemming and common vole were the most abundant small mammal species across the Eurasian Late Pleistocene steppe-tundra environment. Previous ancient DNA studies of the collared lemming and common vole have revealed dynamic population histories shaped by climatic fluctuations. To investigate the extent to which species with similar adaptations share common evolutionary histories, we generated a dataset comprised the mitochondrial genomes of 139 ancient and 6 modern narrow-headed voles from several sites across Europe and northwestern Asia covering approximately the last 100 thousand years (kyr). We inferred Bayesian time-aware phylogenies using 11 radiocarbon-dated samples to calibrate the molecular clock. Divergence of the main mtDNA lineages across the three species occurred during marine isotope stages (MIS) 7 and MIS 5, suggesting a common response of species adapted to open habitat during interglacials. We identified several time-structured mtDNA lineages in European narrow-headed vole, suggesting lineage turnover. The timing of some of these turnovers was synchronous across the three species, allowing us to identify the main drivers of the Late Pleistocene dynamics of steppe- and cold-adapted species.

Ground squirrels were an important member of the Pleistocene steppe-tundra mammal community. They evolved ecological specialisations and exhibit behaviours that make them particularly informative subjects to study palaeoenvironmental constraints affecting species distribution and speciation. Interspecific competition and isolating geographical barriers are considered as the principal factors that define species range boundaries.The present paper provides a first comprehensive compilation of the living and extinct Spermophilus species in Europe. These data suggest 'patchwork quilt' model for the expansion and spatial distribution of ground squirrel species. Here we consider mainly small-sized Spermophilus species because large-sized (e.g., S. superciliosus) ground squirrels consist another 'patchwork quilt', which overlap the first one. This overlapping of the species ranges is possible because of the size difference that lowers interspecific competition (Hutchinson's rule).We consider two main types of range boundaries. One type includes roughly 'sub-parallel' boundaries that oscillate in concert with climatic and vegetational changes (a case of climatically controlled competitive exclusion). The other type consists of roughly 'sub-meridional' boundaries corresponding to geographical barriers (e.g., water barriers, mountain ridges); these boundaries are rather stable. Examples of 'sub-parallel range modifications include: oscillations of boundaries between S. pygmaeus and S. suslicus; the immigration of S. citellus into the Pre-Carpathian area; the branching of S. suslicus from S. pygmaeus; the regional appearance of the Late Pleistocene species S. severskensis and S. citelloides. Examples of 'sub-meridional events' are: the crossing of the Danube by S. citellus; the appearance of an isolated population of S. pygmaeus on right bank of the Dnieper during the Late Pleistocene to Middle Holocene; a crossing of the Dnieper river by S. pygmaeus, which resulted in the appearance of S. odessanus; the intrusion of eastern populations of S. pygmaeus into the Trans-Volga areas.

No abstract

No abstract

No abstract