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9 results for “parapatric speciation”
Patterns of Speciation in a Parapatric Pair of Saturnia Moths as Revealed by Target Capture
<p>This is the dataset for the manuscript entitled Patterns of Speciation in a Parapatric Pair of Saturnia Moths as Revealed by Target Capture. This study helps in the delimitation of a parapatric pair of two species of moths in a complex distribution considering their evolutionary history with the help of the Target Capture method.</p>
Data from: A low-latitude species pump: Peripheral isolation, parapatric speciation and mating-system evolution converge in a marine radiation
<p><span>Geologically recent radiation can shed light on speciation processes, but incomplete lineage sorting and introgressive gene flow render accurate evolutionary reconstruction and interpretation challenging. Independently evolving metapopulations of low-dispersal taxa may provide an additional level of phylogeographic information, given sufficiently broad sampling and genome-wide sequencing. Evolution in the marine brown algal genus </span><span>Fucus</span><span> in the south-eastern Atlantic was shaped by Quaternary climate-driven range shifts. Over this timescale, divergence and speciation occurred against a background of expansion-contraction cycles from multiple refugia, together with mating-system shifts from outcrossing (dioecy) to selfing hermaphroditism. We tested the hypothesis that peripheral isolation of range edge (dioecious) </span><span>F. vesiculosus</span><span> led to parapatric speciation and radiation of hermaphrodite lineages. Species tree methods using 876 single-copy nuclear genes and extensive geographic coverage produced conflicting topologies with respect to geographic clades of </span><span>F. vesiculosus</span><span>. All methods, however, revealed a new and early diverging hermaphrodite species, </span><span>Fucus macroguiryi</span><span> sp. Nov. Both the multispecies coalescent and polymorphism-aware models (in contrast to concatenation) support sequential paraphyly in </span><span>F. vesiculosus</span><span> resulting from distinct evolutionary processes. Our results support 1) peripheral isolation of the southern </span><span>F. vesiculosus</span><span> clade prior to parapatric speciation and radiation of hermaphrodite lineages – a "low latitude species pump". 2) Directional introgressive gene flow into </span><span>F. vesiculosus</span><span> around the present-day secondary contact zone (sympatric-allopatric boundary) between dioecious/hermaphrodite lineages as hermaphrodites expanded northwards, as supported by concordance analysis and statistical tests of introgression. Species boundaries in the extensive sympatric range are likely maintained by reproductive system (selfing in hermaphrodites) and reinforcement.</span></p>
Data from: A low-latitude species pump: Peripheral isolation, parapatric speciation and mating-system evolution converge in a marine radiation
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Data from: A parapatric propensity for breeding precludes the completion of speciation in common teal (Anas crecca, sensu lato)
Speciation is a process in which genetic drift and selection cause divergence over tSpeciation is a process in which genetic drift and selection cause divergence over time. However, there is no rule dictating the time required for speciation, and even low levels of gene flow hinder divergence, so that taxa may be poised at the threshold of speciation for long periods of evolutionary time. We sequenced mitochondrial DNA (mtDNA) and eight nuclear introns (nuDNA) to estimate genomic levels of differentiation and gene flow between the Eurasian common teal (Anas crecca crecca) and the North American green-winged teal (A. c. carolinensis). These ducks come into contact in Beringia (northeastern Asia and northwestern North America) and have likely done so, perhaps cyclically, since the Pliocene-Pleistocene transition, ~2.6 Ma, when they apparently began diverging. They have diagnosable differences in male plumage and are 6.9% divergent in the mtDNA control region, with only 1 of 58 crecca and 2 of 86 carolinensis having haplotypes grouping with the other. Two nuclear loci were likewise strongly structured between these teal (ΦST > 0.35), but six loci were undifferentiated or only weakly structured (ΦST = 0.0–0.06). Gene flow between crecca and carolinensis was ~1 individual per generation in both directions in mtDNA, but was asymmetrical in nuDNA, with ~1 and ~20 individuals per generation immigrating into crecca and carolinensis, respectively. This study illustrates that species delimitation using a single marker oversimplifies the complexity of the speciation process, and it suggests that even with divergent selection, moderate levels of gene flow may stall the speciation process short of completion.
Data from: A parapatric propensity for breeding precludes the completion of speciation in common teal (Anas crecca, sensu lato)
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Data from: Parapatric speciation in three islands: dynamics of geographical configuration of allele sharing
We studied the time to speciation by geographical isolation for a species living on three islands connected by rare migration. We assumed that incompatibility was controlled by a number of quantitative loci and that individuals differing in loci by more than a threshold did not mix genetically with each other. For each locus, we defined the geographical configuration (GC), which specifies islands with common alleles, and traced the stochastic transitions between different GCs. From these results, we calculated the changes in genetic distances. As a single migration event provides an opportunity for transitions in multiple loci, the GCs of different loci are correlated, which can be evaluated by constructing the stochastic differential equations of the number of loci with different GCs. Our model showed that the low number of incompatibility loci facilitates parapatric speciation and that migrants arriving as a group shorten the waiting time to speciation compared with the same number of migrants arriving individually. We also discuss how speciation rate changes with geographical structure.
Data from: Bounds to parapatric speciation: A dobzhansky-muller incompatibility model involving autosomes, X chromosomes and mitochondria
We investigate the conditions for the origin and maintenance of postzygotic isolation barriers, so called (Bateson-)Dobzhansky-Muller incompatibilities or DMIs, among populations that are connected by gene flow. Specifically, we compare the relative stability of pairwise DMIs among autosomes, X chromosomes, and mitochondrial genes. In an analytical approach based on a continent-island framework, we determine how the maximum permissible migration rates depend on the genomic architecture of the DMI, on sex bias in migration rates, and on sex-dependence of allelic and epistatic effects, such as dosage compensation. Our results show that X-linkage of DMIs can enlarge the migration bounds relative to autosomal DMIs or autosome-mitochondrial DMIs, in particular in the presence of dosage compensation. The effect is further strengthened with male-biased migration. This mechanism might contribute to a higher density of DMIs on the X chromosome (large X-effect) that has been observed in several species clades. Furthermore, our results agree with empirical findings of higher introgression rates of autosomal compared to X-linked loci.
Data from: Bounds to parapatric speciation: A dobzhansky-muller incompatibility model involving autosomes, X chromosomes and mitochondria
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Data from: Parapatric speciation in three islands: dynamics of geographical configuration of allele sharing
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