scholarly article | Q13442814 |
P356 | DOI | 10.1111/EVO.13251 |
P698 | PubMed publication ID | 28401982 |
P50 | author | Benjamin M Winger | Q64729202 |
P2860 | cites work | The genomic landscape underlying phenotypic integrity in the face of gene flow in crows | Q22065594 |
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Hybridization reveals the evolving genomic architecture of speciation | Q35300005 | ||
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Historical introgression among the American live oaks and the comparative nature of tests for introgression | Q35753164 | ||
Competitive Interactions upon Secondary Contact Drive Elevational Divergence in Tropical Birds | Q35865864 | ||
Powerful methods for detecting introgressed regions from population genomic data | Q35946609 | ||
Sequence Capture versus Restriction Site Associated DNA Sequencing for Shallow Systematics | Q36049287 | ||
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Plumage Genes and Little Else Distinguish the Genomes of Hybridizing Warblers. | Q36108660 | ||
Parapatric genetic introgression and phenotypic assimilation: testing conditions for introgression between Hercules beetles (Dynastes, Dynastinae). | Q36142340 | ||
Shedding Light on the Grey Zone of Speciation along a Continuum of Genomic Divergence | Q36233821 | ||
Reproductive interference between animal species | Q37269153 | ||
Genome-wide evidence for speciation with gene flow in Heliconius butterflies | Q37272429 | ||
The biology of speciation | Q37627903 | ||
Non-monophyly and deep genetic differentiation across low-elevation barriers in a Neotropical montane bird (Basileuterus tristriatus; Aves: Parulidae). | Q39037977 | ||
Divergence with gene flow and fine-scale phylogeographical structure in the wedge-billed woodcreeper, Glyphorynchus spirurus, a Neotropical rainforest bird. | Q39252511 | ||
Ecological and mutation-order speciation in digital organisms | Q40166764 | ||
Changes in sexual signals are greater than changes in ecological traits in a dichromatic group of fishes | Q40216237 | ||
Differential rates of phenotypic introgression are associated with male behavioral responses to multiple signals. | Q40622757 | ||
Hybridization in headwater regions, and the role of rivers as drivers of speciation in Amazonian birds. | Q40814991 | ||
Detection and Polarization of Introgression in a Five-Taxon Phylogeny | Q41049748 | ||
High incidence of "leapfrog" pattern of geographic variation in andean birds: implications for the speciation process | Q45244319 | ||
Plumage and song differences mediate species recognition between incipient flycatcher species of the Solomon Islands. | Q46093204 | ||
The maintenance of phenotypic divergence through sexual selection: An experimental study in barn swallows Hirundo rustica. | Q46513914 | ||
Pervasive reinforcement and the role of sexual selection in biological speciation. | Q46848743 | ||
Hybridization, introgression, and the nature of species boundaries. | Q46848749 | ||
Mutation-order divergence by sexual selection: diversification of sexual signals in similar environments as a first step in speciation | Q46877262 | ||
Gene flow and the maintenance of species boundaries | Q46898074 | ||
Sexual selection accelerates signal evolution during speciation in birds. | Q51223548 | ||
Experimental evolution: Assortative mating and sexual selection, independent of local adaptation, lead to reproductive isolation in the nematode Caenorhabditis remanei. | Q51325622 | ||
Contributions of natural and sexual selection to the evolution of premating reproductive isolation: a research agenda. | Q51508365 | ||
Conditions for mutation-order speciation. | Q51623570 | ||
Speciation has a spatial scale that depends on levels of gene flow. | Q53481720 | ||
Phylogeny and phylogenetic classification of the tyrant flycatchers, cotingas, manakins, and their allies (Aves: Tyrannides) | Q54509753 | ||
Genetic Distance between Populations | Q56881712 | ||
Biogeography of the Andean metaltail hummingbirds: contrasting evolutionary histories of tree line and habitat-generalist clades | Q57227582 | ||
Speciation by selection: A framework for understanding ecology’s role in speciation | Q57429346 | ||
Non-ecological speciation, niche conservatism and thermal adaptation: how are they connected? | Q57886915 | ||
The genomic landscape of species divergence in Ficedula flycatchers | Q22122149 | ||
Biodiversity hotspots for conservation priorities | Q22122401 | ||
Distributional Ecology of New Guinea Birds: Recent ecological and biogeographical theories can be tested on the bird communities of New Guinea | Q28246424 | ||
Evolution of heterogeneous genome differentiation across multiple contact zones in a crow species complex | Q28314914 | ||
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies | Q28658397 | ||
Reproductive isolation between phylogeographic lineages scales with divergence | Q28661948 | ||
The role of glacial cycles in promoting genetic diversity in the Neotropics: the case of cloud forests during the Last Glacial Maximum | Q28709613 | ||
High dispersal ability inhibits speciation in a continental radiation of passerine birds | Q28731963 | ||
The roles of time and ecology in the continental radiation of the Old World leaf warblers (Phylloscopus and Seicercus). | Q28752141 | ||
Widespread Genetic Incompatibilities between First-Step Mutations during Parallel Adaptation of Saccharomyces cerevisiae to a Common Environment | Q28818537 | ||
Phenotypes in phylogeography: Species' traits, environmental variation, and vertebrate diversification | Q28828864 | ||
Sexual Selection, Social Competition, and Speciation | Q29013916 | ||
Mechanisms of Speciation - A Population Genetic Approach | Q29397057 | ||
Arlequin suite ver 3.5: a new series of programs to perform population genetics analyses under Linux and Windows | Q29547183 | ||
Detecting the number of clusters of individuals using the software STRUCTURE: a simulation study | Q29547289 | ||
Testing for ancient admixture between closely related populations | Q29615091 | ||
A robust, simple genotyping-by-sequencing (GBS) approach for high diversity species | Q29616249 | ||
Evidence for ecological speciation and its alternative | Q29617269 | ||
Inference of population splits and mixtures from genome-wide allele frequency data | Q30000828 | ||
Genomics of Rapid Incipient Speciation in Sympatric Threespine Stickleback | Q30388932 | ||
Inferring phylogeny and introgression using RADseq data: an example from flowering plants (Pedicularis: Orobanchaceae) | Q30622154 | ||
How does climate influence speciation? | Q30650134 | ||
Biogeography and spatio-temporal diversification of Selenidera and Andigena toucans (Aves: Ramphastidae). | Q30653761 | ||
Unforeseen Consequences of Excluding Missing Data from Next-Generation Sequences: Simulation Study of RAD Sequences | Q30835203 | ||
Bergmann's rule near the equator: latitudinal clines in body size of an Andean passerine bird | Q31019147 | ||
Inferring speciation history in the Andes with reduced-representation sequence data: an example in the bay-backed antpittas (Aves; Grallariidae; Grallaria hypoleuca s. l.). | Q31024696 | ||
vcfr: a package to manipulate and visualize variant call format data in R. | Q31113882 | ||
Hidden histories of gene flow in highland birds revealed with genomic markers | Q31122630 | ||
Multiscale assessment of patterns of avian species richness | Q31894954 | ||
Historical biogeography and speciation in the neotropical highlands: molecular phylogenetics of the jay genus Cyanolyca | Q33398886 | ||
Ecological explanations for (incomplete) speciation | Q33404772 | ||
The Lande-Kirkpatrick mechanism is the null model of evolution by intersexual selection: implications for meaning, honesty, and design in intersexual signals | Q33633327 | ||
Reanalysis suggests that genomic islands of speciation are due to reduced diversity, not reduced gene flow | Q34420759 | ||
Evaluating the use of ABBA-BABA statistics to locate introgressed loci | Q34740681 | ||
Phylogeography of a morphologically diverse Neotropical montane species, the Common Bush-Tanager (Chlorospingus ophthalmicus). | Q34766127 | ||
Genomics and the origin of species | Q35096185 | ||
P433 | issue | 7 | |
P921 | main subject | speciation | Q39350 |
P1104 | number of pages | 17 | |
P304 | page(s) | 1815-1831 | |
P577 | publication date | 2017-04-12 | |
P1433 | published in | Evolution | Q4038411 |
P1476 | title | Consequences of divergence and introgression for speciation in Andean cloud forest birds | |
P478 | volume | 71 |
Q96954370 | A new species of frog (Terrarana, Strabomantidae, Phrynopus) from the Peruvian Andean grasslands |
Q92101506 | Assessing biological factors affecting postspeciation introgression |
Q51210285 | Digest: For ecologically similar Andean birds, gene flow and plumage uniformity go hand in hand. |
Q111629880 | Even more oak species in Mexico? Genetic structure and morphological differentiation support the presence of at least two specific entities within Quercus laeta |
Q41702260 | Fine scale mapping of genomic introgressions within the Drosophila yakuba clade |
Q51148538 | On geographic barriers and Pleistocene glaciations: Tracing the diversification of the Russet-crowned Warbler (Myiothlypis coronata) along the Andes. |
Q92796628 | Why is Amazonia a 'source' of biodiversity? Climate-mediated dispersal and synchronous speciation across the Andes in an avian group (Tityrinae) |
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