Combined Evidence Reveals the Origin of a Rapid Range Expansion Despite Retained Genetic Diversity and a Weak Founder Effect

IF 3.9 1区 生物学 Q1 BIOCHEMISTRY & MOLECULAR BIOLOGY
Nora M. Bergman, Petteri Lehikoinen, Edward Kluen, Staffan Bensch, Camilla Lo Cascio Sætre, Fabrice Eroukhmanoff, Frode Fossøy, Petr Procházka, William J. Smith, Bård G. Stokke, Craig R. Primmer, Rose Thorogood, Katja Rönkä
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Abstract

Many species are currently experiencing range shifts in response to changing environmental conditions with potentially serious genetic consequences. Repeated founder events and strong genetic drift are expected to erode genetic variation at the range front, reducing adaptive potential and slowing or even halting the expansion. However, the severity of these consequences for common and highly mobile species undergoing environment-driven range shifts (c.f. invasions) is less clear. Here, we combined historical observations and contemporary movement data of the common reed warbler (Acrocephalus scirpaceus) with genomic evidence from across its European breeding range to (1) infer the origin and (2) quantify the genetic consequences of a recent and rapid northward range expansion. Although there were no reductions in levels of nucleotide diversity or allelic richness, nor a signal of founder effect in the directionality index (ψ), our combined dataset approach was able to infer an expansion origin from the southwest. Furthermore, we found that private allelic richness retained a slight but significant linear decline along the colonisation route. These results suggest that high dispersal capabilities can allow even philopatric species to avoid the loss of genetic diversity during rapid range expansions. Nevertheless, if multiple lines of evidence enable identification of an expansion pathway, we may still detect genetic signals of expansion.

Abstract Image

Abstract Image

综合证据揭示了尽管保留了遗传多样性和微弱的奠基者效应,但快速范围扩张的起源。
许多物种目前正经历着范围的变化,以应对不断变化的环境条件,这可能带来严重的遗传后果。重复的创始者事件和强烈的遗传漂变预计会侵蚀范围前沿的遗传变异,降低适应潜力,减缓甚至停止扩张。然而,对于经历环境驱动的范围转移(如入侵)的普通和高流动性物种,这些后果的严重程度尚不清楚。在这里,我们结合了历史观察和当代芦苇莺(Acrocephalus scirpaceus)的运动数据,以及来自其整个欧洲繁殖范围的基因组证据,以(1)推断其起源,(2)量化最近快速向北扩展的遗传后果。尽管核苷酸多样性或等位基因丰富度水平没有降低,方向性指数(ψ)也没有奠基者效应的信号,但我们的综合数据集方法能够推断出来自西南的扩张起源。此外,我们发现私人等位基因丰富度沿着殖民路线保持了轻微但显著的线性下降。这些结果表明,高扩散能力甚至可以使嗜爱物种在快速范围扩张期间避免遗传多样性的丧失。尽管如此,如果多种证据能够确定扩展途径,我们仍然可以检测到扩展的遗传信号。
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来源期刊
Molecular Ecology
Molecular Ecology 生物-进化生物学
CiteScore
8.40
自引率
10.20%
发文量
472
审稿时长
1 months
期刊介绍: Molecular Ecology publishes papers that utilize molecular genetic techniques to address consequential questions in ecology, evolution, behaviour and conservation. Studies may employ neutral markers for inference about ecological and evolutionary processes or examine ecologically important genes and their products directly. We discourage papers that are primarily descriptive and are relevant only to the taxon being studied. Papers reporting on molecular marker development, molecular diagnostics, barcoding, or DNA taxonomy, or technical methods should be re-directed to our sister journal, Molecular Ecology Resources. Likewise, papers with a strongly applied focus should be submitted to Evolutionary Applications. Research areas of interest to Molecular Ecology include: * population structure and phylogeography * reproductive strategies * relatedness and kin selection * sex allocation * population genetic theory * analytical methods development * conservation genetics * speciation genetics * microbial biodiversity * evolutionary dynamics of QTLs * ecological interactions * molecular adaptation and environmental genomics * impact of genetically modified organisms
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