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Data from: Contact zone dynamics during early stages of speciation in a chorus frog (Pseudacris crucifer)
负责人:
关键词:
evolutionary lineages;asymmetrical hybridization;Pseudacris crucifer;reproductive isolation;cryptic diversity;range fragmentation;clines
DOI:
doi:10.5061/dryad.8h06d
摘要:
x divergent mitochondrial DNA (mtDNA) lineages, many of which came into secondary contact during the Holocene. We examined genetics, morphology
Data from: The hidden history of the snowshoe hare, Lepus americanus: extensive mitochondrial DNA introgression inferred from multilocus genetic variation
负责人:
关键词:
Lagomorphs;Hares and jackrabbits;Lepus americanus;coalescent;Lepus californicus;Cryptic divegence;Species tree;Lepus townsendii;Pliocene;Holocene;reticulate evolution;Pleistocene
DOI:
doi:10.5061/dryad.21f62
摘要:
) and the black-tailed jackrabbit (L. californicus) - by analyzing sequence variation at eight nuclear markers and one mitochondrial DNA (mtDNA) locus (6 240 bp; 94
Data from: Populations at risk: conservation genetics of kangaroo mice (Microdipodops) of the Great Basin Desert
负责人:
关键词:
microsatellites;population genetics;kangaroo mice;Microdipodops;Microdipodops pallidus;Microdipodops megacephalus;historical biogeography;Great Basin Desert;effective population size;Holocene;Pliocene;Pleistocene
DOI:
doi:10.5061/dryad.r531f
摘要:
anthropogenic impacts, with the more recent alterations likely resulting in the decline of native fauna and flora. Dark (Microdipodops megacephalus) and palli
Data from: Speciation in Western Scrub-Jays, Haldane’s rule, and genetic clines in secondary contact
负责人:
关键词:
post-zygotic reproductive barriers;gene flow;Neogene;Aphelocoma californica;Birds;Pliocene;speciation;phylogeography;Aphelocoma;Corvidae;Aves;Holocene;Pleistocene
DOI:
doi:10.5061/dryad.57f48
摘要:
st of studies that support predictions of Haldane’s Rule using cline analysis of multiple loci of differing inheritance modes, although alternate hypotheses li
Data from: Rates of evolution: a quantitative synthesis
负责人:
关键词:
Brachycrus wilsoni;Mesozoic;Otomys auretus;Experimental Selection;Paleocene;Longitudinal time series;Merycochoerus proprius;Ectocion parvus;Passer montanus;Petrochelidon pyrrhonota;Metrarabdotos volkesorum;Metrarabdotos cubaguaense;Anolis carolinensis;Anakosmoceras sp.;Globoratalia tumida;Oligocene;Cervus elaphus;Rattus rattus;Ursavus elmensis;Merychippus paniensis;Longitudinal field study;cross-sectional field study;Merychyus elegans;Mesohippus bairdi;Hyracotherium sandrae;Hyopsodus latidens;Cantius trigonodus;Cantius ralstoni;Kosmoceras sp.;Passer domesticus;Pliocene;Merycochoerus matthewi;Stephanodiscus yellowstonensis;Eocoelia sp.;Hyopsodus pauxillus;Jurassic;Merychyus crabilli;Neotoma albigula;Branta leucopsis;Scathophaga stercoraria;Mus sp.;Metrarabdotos colligatum;Peromyscus maniculatus;Loxodonta sp.;Mollusca;Holocene;Mesomyla sclateri;Homo erectus;Brassica rapa;Mammuthus sp.;Artificial selection;Haplomylus simpsoni;Cormohipparion occidentale;Peromyscus leucopus;Cosomys primus;Hyracotherium grangeri;Parapelomys sp.;Globorotalia conoidea;Eohippus resartus;Vulpes vulpes;Hyopsodus miticulus;Zea mays;Dipodomys merriami;Urocitellus beldingi;Amara quenseli;Eocene;Herpestes auropunctatus;Otomys angoniensis;Hyopsodus powellianus;Hirundo rustica;Elephas sp.;Poseidonamicus spp.;Paleozoic;Primelephas sp.;Euryderus grossus;Globoratalia plesiotumida;Merychyus relictus;Ursus etruscus;Cantius mckennai;Gyretes sinuatus;Gambusia affinis;Globorotalia inflata;Gasterosteus aculeatus;Pleistocene;Drepanis coccinea;Gymnodactylus amarali;Carabus nemoralis;Chlorocebus sabaeus;Experimental field study;Ursus spelaeus;Myzomela pammelaena;Cymindis planipennis;Thymallus thymallus;Ectocion ralstonensis;Haplomylus speirianus;Pseudocubus vema;Pterostichus algidus;Dinosauria;Pterostichus melanarius;Equus germanicus;Cenozoic;Globorotalia puncticulata;Gallus gallus;Merychyus minimus;Cryptopecten vesicululosus;Equidae;Hyopsodus minor;Hyracotherium borealis;Oncorhyncus nerka;Ovis aries;Fringilla coelebs;fossil record;Anser caerulescens;Haplomylus scottianus;drosophila melanogaster;Brachycrus siouense;Cantius torresi;Hyopsodus lysitensis;Ficedula albicollis;Ectocion osbornianus;Mus musculus;Silurian;Bison bison;Metrarabdotos saundersi;Zugokosmoceras sp.;Bison priscus;Metrarabdotos auriculatum;Bison latifrons;Mandarina chichijimana;Gasterosteus doryssus;Geospiza scandens;Scaphinotus angusticollis;Telespyza canans;Recent;Oryctolagus cuniculus;Jadera haematoloma;Antemus sp.;Hyopsodus loomisi;Progonomys sp.;Drosophila subobscura;Harpalus fraternus;introduced species;Laboratory selection;Haplomylus palustris;Haplomylus zalmouti;Cyclostephanos andinus;Loxodonta africana;Globorotalia conomiozea;Karnimata sp.;Plethodon spp.;natural selection;Geospiza fortis;Ursus arctos;Bison antiquus;Metrarabdotos boldi;Metrarabdotos coatesi;Drosophila pseudoobscura;Littorina obtusata;Parus caeruleus;Poecilia reticulata;Miocene
DOI:
doi:10.5061/dryad.1tn7123
摘要:
One-generation step intervals, differences, and rates; longer base intervals, differences, and rates; and overlapping net intervals, difference
and species distribution modeling
负责人:
关键词:
refugia;LGM;Nyssa;phylogeography;mid Holocene;Nyssa biflora;RAD-seq;Nyssa sylvatica;Eocene;Miocene;SDM
DOI:
doi:10.5061/dryad.bb3h52t
摘要:
to be in the Pliocene and that of N. biflora-N. ursina mix in the end of the Miocene. Results from SDM predicted a smaller range in the southern part of the species prese

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