Abstract:Dispersal is one of the most important but least understood processes in plant ecology and evolutionary biology. Dispersal of seeds maintains and establishes populations, and pollen and seed dispersal are responsible for gene flow within and among populations. Traditional views of dispersal and gene flow assume models that are governed solely by geographic distance and do not account for variation in dispersal vector behavior in response to heterogenous landscapes. Landscape genetics integrates population gene… Show more
“…Due to the spatial configuration of these populations, we also (d) tested the central-marginal hypothesis (CMH), which predicts decreased gene flow and increased pairwise genetic differentiation among populations towards the edge of the species range (Micheletti & Storfer, 2015). Despite the challenges associated with modeling plant landscape genetics due to their sedentary life, and passive seed and pollen dispersal, plant species offer an excellent opportunity to explore species' interactions with the landscape (Alvarado-Serrano et al, 2019;Cruzan & Hendrickson, 2020). Furthermore, plants like I. webberi with short generation times are expected to respond quicker to environmental and landscape changes; these effects can be observed in the distribution of genetic variation within the species (Aguilar et al, 2008).…”
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
“…Due to the spatial configuration of these populations, we also (d) tested the central-marginal hypothesis (CMH), which predicts decreased gene flow and increased pairwise genetic differentiation among populations towards the edge of the species range (Micheletti & Storfer, 2015). Despite the challenges associated with modeling plant landscape genetics due to their sedentary life, and passive seed and pollen dispersal, plant species offer an excellent opportunity to explore species' interactions with the landscape (Alvarado-Serrano et al, 2019;Cruzan & Hendrickson, 2020). Furthermore, plants like I. webberi with short generation times are expected to respond quicker to environmental and landscape changes; these effects can be observed in the distribution of genetic variation within the species (Aguilar et al, 2008).…”
This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
“…IBR takes this effect into account in addition to the geographic distance and can therefore be considered an extension of the simple IBD model. IBR is particularly important for plants because they cannot easily move through inhabitable areas like cities, cropland or large water bodies and was found to be a better predictor of plants dispersal capabilities than IBD (Cruzan & Hendrikson, 2020, Grasty et al, 2020). Besides those processes that directly affect geneflow patterns among populations, the demographic history of a species can indirectly influence the genetic differentiation between populations.…”
Genetic diversity a major determinant for the capacity of species to persist and adapt to their environments. Unraveling the factors affecting genetic differentiation is crucial to understand how genetic diversity is shaped and species may react to changing environments. We employed genotyping by sequencing to test the influence of climate, space, latitude, altitude and land cover on genetic differentiation in a collection of 81 wild pea samples (Pisum sativum ssp. elatius) from across its distribution range from western Europe to central Asia. We also attempted to elucidate the species recent evolutionary history and its effect on the current distribution of genetic diversity. Association of single SNPs with climate variables were analyses to test for signatures of local adaptation. Genetic variation was geographically structured into six distinct genetic cluster. Two of which were associated with a taxonomic group (Pisum sativum ssp. humile) that according to some researchers does not qualify for a sub-species rank due to its alleged lack of genetic distinctness from other conspecific groups. The effect of the tested factors influencing genetic differentiation were rather variable among genetic clusters. The climate predictors were most important in all clusters. Land use was more important in clusters from areas strongly influenced by human land use, especially by agriculture. We found a statistically significant association of 3,623 SNPs (2.4 % of all SNPs) with one of the environmental predictors. Most of them were correlated with latitude followed by temperature, precipitation and altitude. Estimation of SNP effects of the candidates resulted in a missense to silent ratio of 0.45, suggesting many of the observed candidates SNPs may alter the encoded amino acid sequence. Wild peas went through a genetic bottleneck during the last glacial period followed by population recovery. Probably associated with this population recovery, we detected a range expansion, which may have led to an eastward range expansion of the European cluster to Turkey and thereof southwards and eastwards. Overall, the interplay of several environmental factors and the recent evolutionary history affected the distribution of genetic diversity in wild peas where each subpopulations were differently affected by those factors and processes.
“…Gene flow depends on the landscape structure, mating system, pollination vectors and the adaptations of seeds for dispersal (Schmidt et al 2009, Buehler et al 2012, Sork et al 1999, Cruzan and Hendrickson 2020). The naturally fragmented structure of our study area, where large bodies of water separate islands only some of which have suitable habitats for V. hirundinaria , suggests that there are obstacles for successful gene flow.…”
Fragmented landscapes may have implications for the genetic structure of populations and for the microevolution of plant species. In particular, landscape fragmentation and/or population isolation might affect the evolution of plant mating systems. Here, we study the consequences of landscape fragmentation on the genetic structure of populations of a perennial herb, Vincetoxicum hirundinaria with a mixed mating system. Our study area, the south‐western Finnish archipelago, was formed after the glacial ice sheet started to retreat 12 000 years ago. Due to the isostatic land uplift following the glacial retreat, suitable habitats have been formed gradually, and as a consequence, populations of V. hirundinaria differ in age, size and their degree of isolation in the area. We hypothesized that a mixed‐mating system has been selected for in these populations due to the advantage of self‐fertilization in newly colonized areas and the advantage of outcrossing in adaptation to heterogeneous environments. To test this hypothesis, we collected seeds of open‐pollinated flowers from 13 V. hirundinaria populations differing in size, age and isolation, and used 15 microsatellite markers to perform progeny‐array analysis to estimate population‐level outcrossing rates, population genetic indices and population structure. We found that V. hirundinaria is almost completely outcrossing in the study area with no signs of past self‐fertilization and/or mating among relatives. The overall low inbreeding coefficients indicate that even in small populations mating among relatives is rare. High allelic richness of both maternal and offspring genotypes as well as limited genetic differentiation among the studied populations indicate strong gene flow among them. Our findings suggest that V. hirundinaria has successful seed and pollen dispersal among populations that has allowed colonization of new habitats in this fragmented landscape and led to a genetically well‐mixed group of populations at the scale of the study.
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