Abstract
Since the last glacial maximum (LGM), many plant and animal taxa have expanded their ranges by migration from glacial refugia. Weeds of cultivation may have followed this trend or spread globally following the expansion of agriculture or ruderal habitats associated with human‐mediated disturbance. We tested whether the range expansion of the weed Silene vulgaris across Europe fit the classical model of postglacial expansion from southern refugia, or followed known routes of the expansion of human agricultural practices. We used species distribution modeling to predict spatial patterns of postglacial expansion and contrasted these with the patterns of human agricultural expansion. A population genetic analysis using microsatellite loci was then used to test which scenario was better supported by spatial patterns of genetic diversity and structure. Genetic diversity was highest in southern Europe and declined with increasing latitude. Locations of ancestral demes from genetic cluster analysis were consistent with areas of predicted refugia. Species distribution models showed the most suitable habitat in the LGM on the southern coasts of Europe. These results support the typical postglacial northward colonization from southern refugia while refuting the east‐to‐west agricultural spread as the main mode of expansion for S. vulgaris. We know that S. vulgaris has recently colonized many regions (including North America and other continents) through human‐mediated dispersal, but there is no evidence for a direct link between the Neolithic expansion of agriculture and current patterns of genetic diversity of S. vulgaris in Europe. Therefore, the history of range expansion of S. vulgaris likely began with postglacial expansion after the LGM, followed by more recent global dispersal by humans.
Highlights
Determining the limits of species geographic ranges and their movements over time has been a fundamental goal for ecology (MacArthur 1972) and evolutionary biology (Excoffier et al 2009)
Evidence of postglacial expansion is still apparent in the genomes of both A. thaliana and S. vulgaris even though phylogeographic patterns may become obscured by ongoing dispersal and admixture, either as a natural product of secondary contact between different refugia during expansion (Petit et al 2003) or as a result of more recent human-mediated dispersal (Wilson et al 2009)
Postglacial expansion from glacial refugia since the last glacial maximum (LGM) has been supported for a variety of taxa on many different parts of the planet
Summary
Determining the limits of species geographic ranges and their movements over time has been a fundamental goal for ecology (MacArthur 1972) and evolutionary biology (Excoffier et al 2009). Large-scale climate change is known to be important for determining species distribution shifts (Davis and Shaw 2001; McCarty 2001; Walther et al 2002). Evidence for the “expansion–contraction” model (Provan and Bennett 2008) has been observed in the phylogeographic patterns of genetic diversity for terrestrial flora and fauna in Europe and North America (reviewed in Hewitt (2004) and Schmitt (2007)). Multiple historical and environmental factors may structure phylogeographic patterns of genetic diversity. Plastic species that can survive in a wide range of climates may be better able to endure environmental changes in situ, and not adhere to the typical “expansion–contraction” model
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