scholarly article | Q13442814 |
P50 | author | James D. Austin | Q22112163 |
Kelly Zamudio | Q42603898 | ||
P2860 | cites work | IS THE POPULATION SIZE OF A SPECIES RELEVANT TO ITS EVOLUTION? | Q22065713 |
Body size, metabolic rate, generation time, and the molecular clock | Q24563026 | ||
Speciation durations and Pleistocene effects on vertebrate phylogeography | Q24672549 | ||
MEGA4: Molecular Evolutionary Genetics Analysis (MEGA) Software Version 4.0 | Q26778434 | ||
MODELTEST: testing the model of DNA substitution | Q26778437 | ||
MRBAYES: Bayesian inference of phylogenetic trees | Q27860538 | ||
TCS: a computer program to estimate gene genealogies | Q27860935 | ||
DnaSP, DNA polymorphism analyses by the coalescent and other methods | Q27860965 | ||
Statistical methods for detecting molecular adaptation | Q28140163 | ||
The effect of selection on genealogies | Q28250411 | ||
Unbiased estimation of the rates of synonymous and nonsynonymous substitution | Q28266175 | ||
The Reproductive Behavior of the Bullfrog (Rana catesbeiana) | Q56268690 | ||
Post-glacial re-colonization of European biota | Q56784877 | ||
Phylogenetics, zoogeography, and the role of dispersal and vicariance in the evolution of the Rana catesbeiana (Anura: Ranidae) species group | Q57205994 | ||
CRANN: detecting adaptive evolution in protein-coding DNA sequences | Q57241054 | ||
Estimating Divergence Times from Molecular Data on Phylogenetic and Population Genetic Timescales | Q60231619 | ||
Comparative phylogeography of Nearctic and Palearctic fishes | Q60538104 | ||
Pleistocene effects on North American songbird evolution. | Q64991854 | ||
Emergence, Breeding, Hibernation, Movements and Transformation of the Bullfrog, Rana catesbeiana, in Missouri | Q95614178 | ||
Age Estimation, Growth Rates, and Population Structure in Missouri Bullfrogs | Q95625643 | ||
A New Species of Frog (Ranidae: Rana) from Northwestern Florida | Q95636776 | ||
Divergence in mitochondrial DNA of Near Eastern water frogs with special reference to the systematic status of Cypriote and Anatolian populations (Anura, Ranidae) | Q101397348 | ||
Phylogeny of the New World true frogs (Rana) | Q28300033 | ||
Adaptive protein evolution at the Adh locus in Drosophila | Q28302478 | ||
Investigating the evolutionary history of the Pacific Northwest mesic forest ecosystem: hypothesis testing within a comparative phylogeographic framework | Q29299950 | ||
Multilocus methods for estimating population sizes, migration rates and divergence time, with applications to the divergence of Drosophila pseudoobscura and D. persimilis | Q29547348 | ||
Time dependency of molecular rate estimates and systematic overestimation of recent divergence times | Q29547571 | ||
Comparative phylogeography and postglacial colonization routes in Europe | Q29547684 | ||
Integration within the Felsenstein equation for improved Markov chain Monte Carlo methods in population genetics | Q29614321 | ||
The incomplete natural history of mitochondria | Q29616111 | ||
Intraspecific gene genealogies: trees grafting into networks | Q29618607 | ||
PCR primers and amplification methods for 12S ribosomal DNA, the control region, cytochrome oxidase I, and cytochrome b in bufonids and other frogs, and an overview of PCR primers which have amplified DNA in amphibians successfully | Q30655778 | ||
Historical isolation, range expansion, and secondary contact of two highly divergent mitochondrial lineages in spotted salamanders (Ambystoma maculatum). | Q30820808 | ||
New mitochondrial DNA data affirm the importance of Pleistocene speciation in North American birds | Q30939839 | ||
Mitochondrial DNA phylogeography of the polytypic North American rat snake (Elaphe obsoleta): a critique of the subspecies concept | Q30981535 | ||
Phylogenetic relationships of the North American chorus frogs (Pseudacris: Hylidae). | Q31035164 | ||
Habitat fragmentation and biodiversity: testing for the evolutionary effects of refugia | Q31097227 | ||
Evolutionary rates, divergence dates, and the performance of mitochondrial genes in Bayesian phylogenetic analysis | Q33239787 | ||
Population size does not influence mitochondrial genetic diversity in animals | Q33241444 | ||
Selective neutrality of mitochondrial ND2 sequences, phylogeography and species limits in Sitta europaea | Q33244283 | ||
Mitochondrial DNA under siege in avian phylogeography | Q33327289 | ||
Methods to detect selection in populations with applications to the human | Q34101053 | ||
Molecular systematics of the eastern fence lizard (Sceloporus undulatus): a comparison of parsimony, likelihood, and Bayesian approaches | Q34122932 | ||
Controlling for the effects of history and nonequilibrium conditions in gene flow estimates in northern bullfrog (Rana catesbeiana) populations. | Q34569645 | ||
Nonneutral evolution at the mitochondrial NADH dehydrogenase subunit 3 gene in mice | Q35570984 | ||
MtDNA phylogeography of the California newt, Taricha torosa (Caudata, Salamandridae). | Q36812286 | ||
Excess amino acid polymorphism in mitochondrial DNA: contrasts among genes from Drosophila, mice, and humans | Q38562605 | ||
Comparative phylogeography of eastern chipmunks and white-footed mice in relation to the individualistic nature of species | Q42601359 | ||
Comparative phylogeography of unglaciated eastern North America | Q44924354 | ||
Molecular phylogenetics of western North American frogs of the Rana boylii species group. | Q45994300 | ||
Congruence, consensus, and the comparative phylogeography of codistributed species in California | Q46137523 | ||
Range-wide phylogeography of a temperate lizard, the five-lined skink (Eumeces fasciatus). | Q47296837 | ||
Discordant temporal and geographic patterns in maternal lineages of eastern North American frogs, Rana catesbeiana (Ranidae) and Pseudacris crucifer (Hylidae). | Q47307011 | ||
Mitochondrial DNA rates and biogeography in European newts (genus Euproctus). | Q48052793 | ||
Phylogeographic incongruence of codistributed amphibian species based on small differences in geographic distribution. | Q51928533 | ||
An algorithm for detecting directional and non-directional positive selection, neutrality and negative selection in protein coding DNA sequences. | Q52026897 | ||
Natural selection on mitochondrial DNA in Parus and its relevance for phylogeographic studies. | Q55398285 | ||
Territoriality and Male Mating Success in the Green Frog (Rana Clamitans) | Q55886230 | ||
The Nearly Neutral Theory of Molecular Evolution | Q55968685 | ||
Evolutionary Relationships Within the Ensatina Eschscholtzii Complex Confirm the Ring Species Interpretation | Q55980373 | ||
The Food and Feeding Behavior of the Green Frog, Rana clamitans Latreille, in New York State | Q56037768 | ||
P433 | issue | 3 | |
P921 | main subject | Ranidae | Q6408 |
P1104 | number of pages | 13 | |
P304 | page(s) | 1041-1053 | |
P577 | publication date | 2008-06-24 | |
P1433 | published in | Molecular Phylogenetics and Evolution | Q4248868 |
P1476 | title | Incongruence in the pattern and timing of intra-specific diversification in bronze frogs and bullfrogs (Ranidae). | |
P478 | volume | 48 |
Q104500339 | Cytonuclear discordance, reticulation and cryptic diversity in one of North America's most common frogs |
Q34504176 | High genetic diversity but low population structure in the frog Pseudopaludicola falcipes (Hensel, 1867) (Amphibia, Anura) from the Pampas of South America |
Q116205973 | Morphological and molecular evidence indicates that the Gulf Coast box turtle (Terrapene carolina major) is not a distinct evolutionary lineage in the Florida Panhandle |
Q28647367 | Phylogeography of Nanorana parkeri (Anura: Ranidae) and multiple refugia on the Tibetan Plateau revealed by mitochondrial and nuclear DNA |
Q42651560 | Rapid range expansion in the Great Plains narrow-mouthed toad (Gastrophryne olivacea) and a revised taxonomy for North American microhylids |
Q39035172 | The relative roles of vicariance versus elevational gradients in the genetic differentiation of the high Andean tree frog, Dendropsophus labialis. |
Search more.