Current distributions of widespread North American (NA) species have been shaped by Pleistocene glacial cycles, latitudinal temperature gradients, sharp longitudinal habitat transitions and the vicariant effects of major mountain and river systems that subdivide the continent. Within these transcontinental species, genetic diversity patterns might not conform to established biogeographic breaks compared to more spatially restricted taxa due to intrinsic differences or spatiotemporal differences. In this study, we highlight the effects of these extrinsic variables on genetic structuring by investigating the phylogeographic history of a widespread generalist squamate found throughout NA.
North America.
Common gartersnake,
We evaluate the effects of major river basins and the forest‐grassland transition into the Interior Plains on genetic structure patterns using phylogenetic, spatially informed population structure and demographic analyses of single nucleotide polymorphism data and address range expansion history with ecological niche modelling using locality and historic climate data.
We identify four phylogeographic lineages with varying degrees of connectivity between them. We find discordant population structure patterns between sex‐linked and autosomal loci with respect to the relationship between the central NA lineage relative to coastal lineages. We find support for southeast Pleistocene refugia where recent secondary contact occurred during the Last Glacial Maximum and evidence for both northern and southern refugia in western NA.
Our results provide strong evidence for a Pliocene origin for
We used genome‐scale sampling to assess the phylogeography of a group of topminnows in the
Central and southern United States including drainages of the Gulf of Mexico Coastal Plain and portions of the Mississippi River drainage in and around the Central Highlands.
Topminnows, Genus
We sampled members of the
Genetic data are presented for 749 individuals sampled from 14
Populations of
Across eastern North America, glacial cycles of the Pleistocene drove episodic latitudinal range shifts by temperate species. Isolation of populations within low-latitude refugia during glacial maxima was enhanced by physiographic barriers, leading to patterns of phylogeographic differentiation that are shared across diverse taxa. Postglacial population expansion created opportunities for differentiated lineages to come into contact, with various potential population-genetic outcomes. Northern short-tailed shrews (Blarina brevicauda) exhibit three mitochondrial phylogroups that probably originated via glacial-age range restriction and isolation. We investigate the history of postglacial expansion and interlineage contact between historically isolated regional populations of B. brevicauda. Morphological differences between skulls of shrews representing a Western lineage and those representing Central and Eastern lineages are consistent with past subspecies delineations. However, we demonstrate broad range overlap between neighboring phylogroups across the Upper Peninsula and Lower Peninsula in Michigan. Further, incongruence between phylogroup association and morphology among individuals in Upper Peninsula populations suggests that genetic admixture between shrews representing the Western and Central groups has occurred in the past and may be ongoing. We show that across most cranial measurements, shrews within the contact zone are morphologically most similar to the Central group regardless of mitochondrial identity, but one measurement in these contact zone shrews (depth of skull) is more similar to that seen in the Western group. These results suggest that hybridization between historically isolated populations has resulted in the origin of a novel skull phenotype that is proportionally deeper, narrower, and shorter than those seen in core Western and Central populations.
To investigate the cryptic diversity and diversification timing in the putatively low‐dispersal Amazonian leaf‐litter lizard
Central Amazonia, Brazil.
Squamata; Gymnophthalmidae;
We sequenced two mitochondrial and two nuclear markers in 157 individuals. Phylogeographic structure and the occurrence of independent evolving lineages where explored through phylogenetic and coalescent analyses. A species tree and divergence dates of lineages were inferred with *BEAST, employing multiple DNA substitution rates. The potential genetic impacts of geographical distance among localities, the environment and the position of localities in relation to main rivers were tested by redundancy analysis (RDA).
We detected 11 independently evolving and largely divergent intraspecific lineages. Lineage distribution patterns are complex and do not match any conspicuous barrier to gene flow, except for the Amazon River. Most lineages appear to have originated in the lower Miocene and Pliocene, in disagreement with the Pleistocene refuge hypothesis. IBD, IBE and rivers appear to have acted in concert establishing and maintaining genetic structure. However, when controlling for other explanatory variables, IBD explains significantly more variation than rivers, IBE or historical factors.
Our results strongly suggest that
Pleistocene climate and associated environmental changes have influenced phylogeographic patterns of many species. These not only depend on a species’ life history but also vary regionally. Consequently, populations of widespread species that occur in several biomes might display different evolutionary trajectories. We aimed to identify regional drivers of diversification in the common pheasant, a widely distributed ecological generalist.
Asia.
Common pheasant
Using a comprehensive geographical sampling of 204 individuals from the species’ entire range genotyped at seven nuclear and two mitochondrial loci, we reconstructed spatio‐temporal diversification and demographic history of the common pheasant. We applied Bayesian phylogenetic inference to describe phylogeographic structure, generated a species tree and inferred demographic history within and migration between lineages. Moreover, to establish a taxonomic framework, we conducted a species delimitation analysis.
The common pheasant diversified during the Late Pleistocene into eight distinct lineages. It originated at the edge of the Qinghai–Tibetan plateau and spread to East and Central Asia. Only the widely distributed lowland lineage of East Asia displayed recent range expansion. Greater phylogeographic structure was identified elsewhere, with lineages showing no sign of recent demographic changes. One lineage in south‐central China is the result of long‐term isolation within a climatically stable but topographically complex region. In lineages from arid Central Asia and China, range expansions were impeded by repeated population fragmentation during dry glacial periods and by recent aridification.
Spatio‐temporal phylogeographic frameworks of widespread taxa such as the common pheasant provide valuable opportunities to identify divergent drivers of regional diversification. Our results suggest that diversification and population histories in the eight distinct evolutionary lineages were shaped by regionally variable effects of past climate and associated environmental changes. The evolutionary history of the common pheasant is best reflected by its being split into three species.
Species with wide distributions spanning the African Guinean and Congolian rain forests are often composed of genetically distinct populations or cryptic species with geographic distributions that mirror the locations of the remaining forest habitats. We used phylogeographic inference and demographic model testing to evaluate diversification models in a widespread rain forest species, the African foam‐nest treefrog
Guinean and Congolian rain forests, West and Central Africa.
We collected mitochondrial DNA (mtDNA) and single‐nucleotide polymorphism (SNP) data for 130 samples of
Population structure within
Considering historical demography is essential for understanding population diversification, especially in complex landscapes such as those found in the Guineo–Congolian forest. Population demographic inferences help connect the patterns of genetic variation to diversification model predictions. The diversification history of
