An official website of the United States government
Abstract AimTo review the histories of the Colorado River and North American monsoon system to ascertain their effects on the genetic divergence of desert‐adapted animals. LocationLower Colorado River region, including Mojave and Sonoran deserts, United States. MethodsWe synthesized recent geological literature to summarize initiation phases of lower Colorado River evolution, their discrepancies, and potential for post‐vicariance dispersal of animals across the river. We simulated data under geological models and performed a meta‐analysis of published and unpublished genetic data including population diversity metrics, relatedness and historical migration rates to assess alternative divergence hypotheses. ResultsThe two models for arrival of the Colorado River into the Gulf of California impose east‐west divergence ages of 5.3 and 4.8 Ma, respectively. We found quantifiable river‐associated differentiation in the lower Colorado River region in reptiles, arachnids and mammals relative to flying insects. However, topological statistics, historical migration rates and cross‐river extralimital populations suggest that the river should be considered a leaky barrier that filters, rather than prevents, gene flow. Most markers violated neutrality tests. Differential adaptation to monsoon‐based precipitation differences may contribute to divergence between Mojave and Sonoran populations and should be tested. Main ConclusionsRivers are dynamic features that can both limit and facilitate gene flow through time, the impacts of which are mitigated by species‐specific life history and dispersal traits. The Southwest is a geo‐climatically complex region with the potential to produce pseudocongruent patterns of genetic divergence, offering a good setting to evaluate intermediate levels of geological‐biological (geobiological) complexity.
more »
« less
Efficient summary statistics for detecting lineage fusion from phylogeographic datasets
Abstract AimLineage fusion (merging of two or more populations of a species resulting in a single panmictic group) is a special case of secondary contact. It has the potential to counteract diversification and speciation, or to facilitate it through creation of novel genotypes. Understanding the prevalence of lineage fusion in nature requires reliable detection of it, such that efficient summary statistics are needed. Here, we report on simulations that characterized the initial intensity and subsequent decay of signatures of past fusion for 17 summary statistics applicable to DNA sequence haplotype data. LocationGlobal. TaxaDiploid out‐crossing species. MethodsWe considered a range of scenarios that could reveal the impacts of different combinations of read length versus number of loci (arrangement of DNA sequence data), and whether or not pre‐fusion populations experienced bottlenecks coinciding with their divergence (historical context of fusion). Post‐fusion gene pools were sampled along 10 successive time points representing increasing lag times following merging of sister populations, and summary statistic values were recalculated at each. ResultsMany summary statistics were able to detect signatures of complete merging of populations after a sampling lag time of 1.5Negenerations, but the most informative ones included two neutrality tests and four diversity metrics, withZnS(a linkage disequilibrium‐based neutrality test) being particularly powerful. Correlation was relatively low among the two neutrality tests and two of the diversity metrics. There were clear benefits of many short (200‐bp × 200) loci over a handful of long (4‐kb × 10) loci. Also, only the latter genetic dataset type showed impacts of bottlenecks during divergence upon the number of informative summary statistics. Main conclusionsThis work contributes to identifying cases of lineage fusion, and advances phylogeography by enabling more nuanced reconstructions of how individual species, or multiple members of an ecological community, responded to past environmental change.
more »
« less
- Award ID(s):
- 1738817
- PAR ID:
- 10456193
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Journal of Biogeography
- Volume:
- 47
- Issue:
- 10
- ISSN:
- 0305-0270
- Page Range / eLocation ID:
- p. 2129-2140
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
PremiseDivergence depends on the strength of selection and frequency of gene flow between taxa, while reproductive isolation relies on mating barriers and geographic distance. Less is known about how these processes interact at early stages of speciation. Here, we compared population‐level differentiation in floral phenotype and genetic sequence variation among recently divergedCastillejato explore patterns of diversification under different scenarios of reproductive isolation. MethodsUsing target enrichment enabled by the Angiosperms353 probe set, we assessed genetic distance among 50 populations of fourCastillejaspecies. We investigated whether patterns of genetic divergence are explained by floral trait variation or geographic distance in two focal groups: the widespreadC. sessilifloraand the more restrictedC. purpureaspecies complex. ResultsWe document thatC. sessilifloraand theC. purpureacomplex are characterized by high diversity in floral color across varying geographic scales. Despite phenotypic divergence, groups were not well supported in phylogenetic analyses, and little genetic differentiation was found across targeted Angiosperms353 loci. Nonetheless, a principal coordinate analysis of single nucleotide polymorphisms revealed differentiation withinC. sessilifloraacross floral morphs and geography and less differentiation among species of theC. purpureacomplex. ConclusionsPatterns of genetic distance inC. sessiliflorasuggest species cohesion maintained over long distances despite variation in floral traits. In theC. purpureacomplex, divergence in floral color across narrow geographic clines may be driven by recent selection on floral color. These contrasting patterns of floral and genetic differentiation reveal that divergence can arise via multiple eco‐evolutionary paths.more » « less
-
Abstract The Andes are a major dispersal barrier for lowland rain forest plants and animals, yet hundreds of lowland tree species are distributed on both sides of the northern Andes, raising questions about how the Andes influenced their biogeographic histories and population genetic structure. To explore these questions, we generated standardized datasets of thousands of SNPs from paired populations of 49 tree species co‐distributed in rain forest tree communities located in Panama and Amazonian Ecuador and calculated genetic diversity (π) and absolute genetic divergence (dXY) within and between populations, respectively. We predicted (1) higher genetic diversity in the ancestral source region (east or west of the Andes) for each taxon and (2) correlation of genetic statistics with species attributes, including elevational range and life‐history strategy. We found that genetic diversity was higher in putative ancestral source regions, possibly reflecting founder events during colonization. We found little support for a relationship between genetic divergence and species attributes except that species with higher elevational range limits exhibited higherdXY, implying older divergence times. One possible explanation for this pattern is that dispersal through mountain passes declined in importance relative to dispersal via alternative lowland routes as the Andes experienced uplift. We found no difference in mean genetic diversity between populations in Central America and the Amazon. Overall, our results suggest that dispersal across the Andes has left enduring signatures in the genetic structure of widespread rain forest trees. We outline additional hypotheses to be tested with species‐specific case studies.more » « less
-
ABSTRACT AimFerns are globally distributed, yet the number of studies examining the historical evolution of African taxa is relatively low. Investigation of the evolution of African fern diversity is critical in order to understand patterns and processes that have global relevance (e.g., the pantropical diversity disparity [PDD] pattern). This study aims to examine when and from where a globally distributed fern lineage arrived in sub‐Saharan Africa, to obtain a better understanding of potential processes contributing to patterns of diversity across the region. LocationGlobal, sub‐Saharan Africa. TaxonAsplenium(Aspleniaceae). MethodsWe analysed five loci from 537Aspleniumtaxa using a maximum likelihood (IQ‐Tree) phylogenetic framework. For age estimation, we performed penalised likelihood as implemented in treePL, and executed a Bayesian analysis using BEAST. Biogeographical analyses were carried out using BioGeoBEARS. ResultsMost dispersals into Africa occurred within the last ~55 myr, with the highest diversity of sub‐Saharan African taxa concentrated in two clades, each of which descended from an Asian ancestor. Additional dispersals to sub‐Saharan Africa can be found throughout the phylogeny. Lastly, potential cryptic species diversity exists withinAspleniumas evidenced by several polyphyletic taxa. Main ConclusionsWe recover multiple dispersals ofAspleniumto sub‐Saharan Africa, with two major lineages likely diversifying after arrival.more » « less
-
Abstract BackgroundGiven the economic and environmental importance of allopolyploids and other species with highly duplicated genomes, there is a need for methods to distinguish paralogs, i.e. duplicate sequences within a genome, from Mendelian loci, i.e. single copy sequences that pair at meiosis. The ratio of observed to expected heterozygosity is an effective tool for filtering loci but requires genotyping to be performed first at a high computational cost, whereas counting the number of sequence tags detected per genotype is computationally quick but very ineffective in inbred or polyploid populations. Therefore, new methods are needed for filtering paralogs. ResultsWe introduce a novel statistic,Hind/HE, that uses the probability that two reads sampled from a genotype will belong to different alleles, instead of observed heterozygosity. The expected value ofHind/HEis the same across all loci in a dataset, regardless of read depth or allele frequency. In contrast to methods based on observed heterozygosity, it can be estimated and used for filtering loci prior to genotype calling. In addition to filtering paralogs, it can be used to filter loci with null alleles or high overdispersion, and identify individuals with unexpected ploidy and hybrid status. We demonstrate that the statistic is useful at read depths as low as five to 10, well below the depth needed for accurate genotype calling in polyploid and outcrossing species. ConclusionsOur methodology for estimatingHind/HEacross loci and individuals, as well as determining reasonable thresholds for filtering loci, is implemented in polyRAD v1.6, available athttps://github.com/lvclark/polyRAD. In large sequencing datasets, we anticipate that the ability to filter markers and identify problematic individuals prior to genotype calling will save researchers considerable computational time.more » « less
