scholarly article | Q13442814 |
P2093 | author name string | Sanderson MJ | |
M. J. Sanderson | |||
P2860 | cites work | The molecular clock of HIV-1 unveiled through analysis of a known transmission history | Q35631348 |
Molecular evidence from the nuclear genome for the time frame of human evolution | Q38558975 | ||
Estimating divergence dates from molecular sequences | Q40862797 | ||
Multigene phylogeny of land plants with special reference to bryophytes and the earliest land plants | Q44003901 | ||
Estimating divergence times in the presence of an overdispersed molecular clock | Q46183840 | ||
Reconstructing shifts in diversification rates on phylogenetic trees | Q46626280 | ||
A Nonparametric Approach to Estimating Divergence Times in the Absence of Rate Constancy | Q55921509 | ||
Body size, metabolic rate, generation time, and the molecular clock | Q24563026 | ||
Origin of the metazoan phyla: molecular clocks confirm paleontological estimates | Q24671837 | ||
Seed plant phylogeny inferred from all three plant genomes: monophyly of extant gymnosperms and origin of Gnetales from conifers | Q24682532 | ||
Estimation of primate speciation dates using local molecular clocks | Q28140490 | ||
Can fast early rates reconcile molecular dates with the Cambrian explosion? | Q28765899 | ||
Estimating the rate of evolution of the rate of molecular evolution | Q29547787 | ||
Performance of a divergence time estimation method under a probabilistic model of rate evolution | Q29615982 | ||
Among-site rate variation and its impact on phylogenetic analyses | Q29616722 | ||
The general stochastic model of nucleotide substitution | Q29617428 | ||
An examination of the constancy of the rate of molecular evolution | Q30011396 | ||
Error, bias, and long-branch attraction in data for two chloroplast photosystem genes in seed plants | Q30592481 | ||
Examining rates and patterns of nucleotide substitution in plants | Q33845473 | ||
Molecular clock calibrations and metazoan divergence dates | Q33873131 | ||
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 101-9 | |
101-109 | |||
P577 | publication date | 2002-01-01 | |
P1433 | published in | Molecular Biology and Evolution | Q1992656 |
P1476 | title | Estimating absolute rates of molecular evolution and divergence times: a penalized likelihood approach | |
Estimating Absolute Rates of Molecular Evolution and Divergence Times: A Penalized Likelihood Approach | |||
P478 | volume | 19 |
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Q28243003 | A phylogenetic framework for the terns (Sternini) inferred from mtDNA sequences: implications for taxonomy and plumage evolution |
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Q57261319 | A test of the utility of DNA barcoding in the radiation of the freshwater stingray genus Potamotrygon (Potamotrygonidae, Myliobatiformes) |
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Q51874364 | Age and spread of the haplochromine cichlid fishes in Africa. |
Q28750229 | Age at first reproduction explains rate variation in the strepsirrhine molecular clock |
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Q28710478 | An independent genome duplication inferred from Hox paralogs in the American paddlefish--a representative basal ray-finned fish and important comparative reference |
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Q24648464 | An overlooked pink species of land iguana in the Galapagos |
Q28752634 | An uncorrelated relaxed-clock analysis suggests an earlier origin for flowering plants |
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Q51593261 | Ancestry and evolution of seasonal migration in the Parulidae. |
Q28240174 | Ancient co-speciation of simian foamy viruses and primates |
Q28748624 | Ancient origin of a Western Mediterranean radiation of subterranean beetles |
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Q28661383 | Delayed colonisation of Acacia by thrips and the timing of host-conservatism and behavioural specialisation |
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Q54802038 | Different Diversification Rates Between Sexual and Asexual Organisms |
Q50487013 | Differential patterns of male and female mtDNA exchange across the Atlantic Ocean in the blue mussel, Mytilus edulis. |
Q47253540 | Discordances between phylogenetic and morphological patterns in alpine leaf beetles attest to an intricate biogeographic history of lineages in postglacial Europe. |
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Q38971727 | Dispersal assembly of rain forest tree communities across the Amazon basin. |
Q34450194 | Dispersal, vicariance, and timing of diversification in Nothonotus darters. |
Q42028157 | Distinguishing coevolution from covicariance in an obligate pollination mutualism: asynchronous divergence in Joshua tree and its pollinators. |
Q28729854 | Distribution of living Cupressaceae reflects the breakup of Pangea |
Q28728281 | Divergence and phylogeny of Firmicutes from the Cuatro Ciénegas Basin, Mexico: a window to an ancient ocean |
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Q56638843 | Divergence time uncertainty and historical biogeography reconstruction - an example from Urophylleae (Rubiaceae) |
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Q58586541 | Divergent trends in functional and phylogenetic structure in reptile communities across Africa |
Q33609228 | Diversification and biogeography of Juniperus (Cupressaceae): variable diversification rates and multiple intercontinental dispersals |
Q47288701 | Diversification in the Andes: age and origins of South American Heliotropium lineages (Heliotropiaceae, Boraginales). |
Q44254096 | Diversification of Lupinus (Leguminosae) in the western New World: derived evolution of perennial life history and colonization of montane habitats |
Q24675773 | Diversification of Neoaves: integration of molecular sequence data and fossils |
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Q28757534 | Diversification of myco-heterotrophic angiosperms: evidence from Burmanniaceae |
Q42014175 | Diversification of the arboreal mice of the genus Habromys (Rodentia: Cricetidae: Neotominae) in the Mesoamerican highlands |
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Q56886404 | Diversification ofChionochloa(Poaceae) and biogeography of the New Zealand Southern Alps |
Q54555601 | Diversification process of stag beetles belonging to the genus Platycerus Geoffroy (Coleoptera: Lucanidae) in Japan based on nuclear and mitochondrial genes |
Q28690585 | Diversification rates have declined in the Malagasy herpetofauna |
Q39591938 | Diversity and niche evolution along aridity gradients in north american lizards (phrynosomatidae). |
Q56942370 | Diversity begets diversity in competition for space |
Q28744558 | Diversity dynamics in New Caledonia: towards the end of the museum model? |
Q33637002 | Diversity dynamics: molecular phylogenies need the fossil record |
Q44675177 | Do arms races punctuate evolutionary stasis? Unified insights from phylogeny, phylogeography and microevolutionary processes |
Q30892696 | Do missing data influence the accuracy of divergence-time estimation with BEAST? |
Q55097759 | Does a plant-eating insect's diet govern the evolution of insecticide resistance? Comparative tests of the pre-adaptation hypothesis. |
Q31096503 | Does niche conservatism promote speciation? A case study in North American salamanders |
Q89881548 | Draft Genome Assembly of Floccularia luteovirens, an Edible and Symbiotic Mushroom on Qinghai-Tibet Plateau |
Q28659112 | Drechslerella stenobrocha genome illustrates the mechanism of constricting rings and the origin of nematode predation in fungi |
Q46558447 | Early Tertiary out-of-India dispersal of Crypteroniaceae: evidence from phylogeny and molecular dating |
Q36173775 | Early and dynamic colonization of Central America drives speciation in Neotropical army ants. |
Q56269586 | Early evolutionary history of the flowering plant family Annonaceae: steady diversification and boreotropical geodispersal |
Q43534323 | Early origin of viviparity and multiple reversions to oviparity in squamate reptiles |
Q34290408 | Ecological limits on diversification of the Himalayan core Corvoidea |
Q35394231 | Ecomorphological variation in male and female wall lizards and the macroevolution of sexual dimorphism in relation to habitat use. |
Q51456519 | Effects of phylogenetic signal on ancestral state reconstruction. |
Q111629101 | Effects of taxon sampling on molecular dating for within-genus divergence events, when deep fossils are used for calibration |
Q42174844 | Efficient Bayesian inference under the structured coalescent |
Q61796024 | Embracing heterogeneity: coalescing the Tree of Life and the future of phylogenomics |
Q80155223 | En bloc duplications, mutation rates, and densities of amino acid changes clarify the evolution of vertebrate alpha-1,3/4-fucosyltransferases |
Q34034143 | Environmental constraints defining the distribution, composition, and evolution of chlorophototrophs in thermal features of Yellowstone National Park |
Q24613753 | Episodic radiations in the fly tree of life |
Q46987467 | Erratic rates of molecular evolution and incongruence of fossil and molecular divergence time estimates in Ostracoda (Crustacea). |
Q39563769 | Establishing a perimeter position: speciation around the Indian Ocean Basin |
Q30566044 | Estimating divergence dates and evaluating dating methods using phylogenomic and mitochondrial data in squamate reptiles |
Q28710463 | Estimating divergence times in large molecular phylogenies |
Q47752149 | Estimating divergence times in large phylogenetic trees |
Q28741945 | Estimating diversification rates: how useful are divergence times? |
Q28754238 | Estimating rates and patterns of morphological evolution from phylogenies: lessons in limb lability from Australian Lerista lizards |
Q28743794 | Estimating the age of fire in the Cape flora of South Africa from an orchid phylogeny |
Q34229048 | Estimation of divergence times in cnidarian evolution based on mitochondrial protein-coding genes and the fossil record. |
Q24673567 | Evaluating alternative hypotheses for the early evolution and diversification of ants |
Q42493013 | Evaluating fossil calibrations for dating phylogenies in light of rates of molecular evolution: a comparison of three approaches |
Q46221832 | Evaluation of Bayesian models of substitution rate evolution--parental guidance versus mutual independence |
Q41490694 | Evidence for an ancient whole genome duplication in the cycad lineage |
Q46009729 | Evidence for genetic association between East Asian and western North American Crataegus L. (Rosaceae) and rapid divergence of the eastern North American lineages based on multiple DNA sequences. |
Q47778112 | Evidence for inefficient selection against deleterious mutations in cytochrome oxidase I of asexual bdelloid rotifers |
Q33774563 | Evidence of constrained phenotypic evolution in a cryptic species complex of agamid lizards |
Q33722639 | Evidence of extreme habitat stability in a Southeast Asian biodiversity hotspot based on the evolutionary analysis of neotenic net‐winged beetles |
Q44496395 | Evolution and biogeography of marine angelfishes (Pisces: Pomacanthidae). |
Q28728730 | Evolution and biogeography of the slipper orchids: Eocene vicariance of the conduplicate genera in the Old and New World Tropics |
Q47176749 | Evolution and diversification of the forest and hypogean ground-beetle genus Trechus in the Canary Islands. |
Q34184388 | Evolution and metabolic significance of the urea cycle in photosynthetic diatoms |
Q28598125 | Evolution of Epiphytism and Fruit Traits Act Unevenly on the Diversification of the Species-Rich Genus Peperomia (Piperaceae) |
Q33254033 | Evolution of Mesobuthus gibbosus (Brullé, 1832) (Scorpiones: Buthidae) in the northeastern Mediterranean region |
Q39426194 | Evolution of a CAM anatomy predates the origins of Crassulacean acid metabolism in the Agavoideae (Asparagaceae). |
Q28653250 | Evolution of climatic niche specialization: a phylogenetic analysis in amphibians |
Q28751313 | Evolution of exceptional species richness among lineages of fleshy-fruited Myrtaceae |
Q28754460 | Evolution of gigantism in amphiumid salamanders |
Q47291971 | Evolution of host specialization in the Adelgidae (Insecta: Hemiptera) inferred from molecular phylogenetics. |
Q45333151 | Evolution of life cycle, colony morphology, and host specificity in the family Hydractiniidae (Hydrozoa, Cnidaria). |
Q21192748 | Evolution of miniaturization and the phylogenetic position of Paedocypris, comprising the world's smallest vertebrate |
Q24629088 | Evolution of modern birds revealed by mitogenomics: timing the radiation and origin of major orders |
Q34043337 | Evolution of molybdenum nitrogenase during the transition from anaerobic to aerobic metabolism |
Q36740032 | Evolution of protein families: is it possible to distinguish between domains of life? |
Q28657890 | Evolution of rapid development in spadefoot toads is unrelated to arid environments |
Q31060574 | Evolution of rattlesnakes (Viperidae; Crotalus) in the warm deserts of western North America shaped by Neogene vicariance and Quaternary climate change |
Q24671123 | Evolution of the army ant syndrome: The origin and long-term evolutionary stasis of a complex of behavioral and reproductive adaptations |
Q28596267 | Evolution of the climatic tolerance and postglacial range changes of the most primitive orchids (Apostasioideae) within Sundaland, Wallacea and Sahul |
Q44306025 | Evolution of the closely related, sex-related genes DM-W and DMRT1 in African clawed frogs (Xenopus) |
Q28821132 | Evolution of the elaborate male intromittent organ of Xiphophorus fishes |
Q33549045 | Evolution of the nocturnal Nearctic Sphaeropthalminae velvet ants (Hymenoptera: Mutillidae) driven by Neogene orogeny and Pleistocene glaciation. |
Q21192745 | Evolution of the parasitic wasp subfamily Rogadinae (Braconidae): phylogeny and evolution of lepidopteran host ranges and mummy characteristics |
Q28764865 | Evolution of the species-rich Cape flora |
Q46501091 | Evolution under pressure and the adaptation of visual pigment compressibility in deep-sea environments. |
Q28960335 | Evolutionary Relationships and Diversification of Stachyuraceae Based on Sequences of Four Chloroplast Markers and the Nuclear Ribosomal ITS Region |
Q47347152 | Evolutionary biology: ferns reawakened |
Q46273159 | Evolutionary cascades induced by large frugivores |
Q21283849 | Evolutionary divergence times in the Annonaceae: evidence of a late Miocene origin of Pseuduvaria in Sundaland with subsequent diversification in New Guinea |
Q92932402 | Evolutionary diversity in tropical tree communities peaks at intermediate precipitation |
Q28649342 | Evolutionary history and leaf succulence as explanations for medicinal use in aloes and the global popularity of Aloe vera |
Q33834723 | Evolutionary history and phylogeographic relationships of shrews from Sorex araneus group |
Q38901437 | Evolutionary history of the butterflyfishes (f: Chaetodontidae) and the rise of coral feeding fishes. |
Q34560262 | Evolutionary origin of highly repetitive plastid genomes within the clover genus (Trifolium). |
Q28661067 | Evolutionary origins and diversification of proteobacterial mutualists |
Q28654450 | Evolutionary origins of human herpes simplex viruses 1 and 2 |
Q29618553 | Evolutionary rates analysis of Leguminosae implicates a rapid diversification of lineages during the tertiary |
Q33239787 | Evolutionary rates, divergence dates, and the performance of mitochondrial genes in Bayesian phylogenetic analysis |
Q34782130 | Evolutionary relationships among food habit, loss of flight, and reproductive traits: life-history evolution in the Silphinae (Coleoptera: Silphidae). |
Q29300642 | Evolutionary response of Caragana (Fabaceae) to Qinghai–Tibetan Plateau uplift and Asian interior aridification |
Q34582748 | Evolutionary systematics in African gerbilline rodents of the genus Gerbilliscus: inference from mitochondrial genes |
Q46566623 | Evolutionary timescale of monocots determined by the fossilized birth-death model using a large number of fossil records |
Q58310258 | Evolutionary transitions towards eusociality in snapping shrimps |
Q54045634 | Evolving Perceptions on the Antiquity of the Modern Avian Tree |
Q28755143 | Exceptional among-lineage variation in diversification rates during the radiation of Australia's most diverse vertebrate clade |
Q34250934 | Expanded phylogenetic and dating analyses of the apples and their relatives (Pyreae, Rosaceae). |
Q34722435 | Experimental evidence that evolutionarily diverse assemblages result in higher productivity |
Q46288145 | Explaining ecosystem multifunction with evolutionary models |
Q58907801 | Exploring Diversification and Genome Size Evolution in Extant Gymnosperms through Phylogenetic Synthesis |
Q46861984 | Exploring new dating approaches for parasites: the worldwide Apodanthaceae (Cucurbitales) as an example |
Q24651677 | Explosive Pleistocene diversification and hemispheric expansion of a "great speciator" |
Q57833798 | Explosive evolution of an ancient group of Cyphophthalmi (Arachnida: Opiliones) in the Balkan Peninsula |
Q28681047 | Explosive radiation in high Andean Hypericum-rates of diversification among New World lineages |
Q28242184 | Extended mitogenomic phylogenetic analyses yield new insight into crocodylian evolution and their survival of the Cretaceous-Tertiary boundary |
Q36353662 | Extinction vs. Rapid Radiation: The Juxtaposed Evolutionary Histories of Coelotine Spiders Support the Eocene-Oligocene Orogenesis of the Tibetan Plateau |
Q42506279 | Extreme gender flexibility: using a phylogenetic framework to infer the evolution of variation in sex allocation, phylogeography, and speciation in a genus of bidirectional sex changing fishes (Lythrypnus, Gobiidae). |
Q55933657 | FOSSIL CALIBRATIONS AND MOLECULAR DIVERGENCE TIME ESTIMATES IN CENTRARCHID FISHES (TELEOSTEI: CENTRARCHIDAE) |
Q27319874 | Fast Dating Using Least-Squares Criteria and Algorithms |
Q33200741 | Ferns diversified in the shadow of angiosperms |
Q53393309 | Fine-scale biogeographical and temporal diversification processes of peacock swallowtails (PapiliosubgenusAchillides) in the Indo-Australian Archipelago |
Q21132481 | First evidence for a massive extinction event affecting bees close to the K-T boundary |
Q28651163 | Five major shifts of diversification through the long evolutionary history of Magnoliidae (angiosperms) |
Q34168678 | Fluctuating environments, sexual selection and the evolution of flexible mate choice in birds |
Q24648722 | Former diversity of Ephedra (Gnetales): evidence from Early Cretaceous seeds from Portugal and North America |
Q42036997 | Fossil-calibrated molecular phylogenies reveal that leaf-mining moths radiated millions of years after their host plants. |
Q33285498 | Fossils, molecules, divergence times, and the origin of lissamphibians |
Q21089841 | Framing the Salmonidae family phylogenetic portrait: a more complete picture from increased taxon sampling |
Q33461743 | Frequent mitochondrial gene introgression among high elevation Tibetan megophryid frogs revealed by conflicting gene genealogies |
Q47142731 | From ground pools to treeholes: convergent evolution of habitat and phenotype in Aedes mosquitoes. |
Q42012406 | From trajectories to averages: an improved description of the heterogeneity of substitution rates along lineages |
Q55950870 | From words to dates: water into wine, mathemagic or phylogenetic inference? |
Q45151208 | Fungi evolution revisited: application of the penalized likelihood method to a Bayesian fungal phylogeny provides a new perspective on phylogenetic relationships and divergence dates of Ascomycota groups |
Q21093398 | Gain and loss of elongation factor genes in green algae |
Q28767952 | Gene transfer from a parasitic flowering plant to a fern |
Q34529648 | Gene trees and species trees: irreconcilable differences |
Q34031511 | Genes encoding plastid acetyl-CoA carboxylase and 3-phosphoglycerate kinase of the Triticum/Aegilops complex and the evolutionary history of polyploid wheat |
Q91854920 | Genetic analysis of the invasive alga Didymosphenia geminata in Southern Argentina: Evidence of a Pleistocene origin of local lineages |
Q30831310 | Genetic elucidation of cryptic and ancient diversity in a group of Australian diplodactyline geckos: the Diplodactylus vittatus complex. |
Q92264353 | Genome Size Evolution Differs Between Drosophila Subgenera with Striking Differences in Male and Female Genome Size in Sophophora |
Q60400193 | Genome expansion and lineage-specific genetic innovations in the forest pathogenic fungi Armillaria |
Q110697298 | Genome-wide ultraconserved elements resolve phylogenetic relationships and biogeographic history among Neotropical leaf-nosed bats in the genus Anoura (Phyllostomidae) |
Q47989098 | Genomic clocks and evolutionary timescales |
Q90387786 | Genomic signature of shifts in selection in a sub-alpine ant and its physiological adaptations |
Q50133583 | Genomics of the origin and evolution of Citrus. |
Q28960393 | Gentianella stiriaca, a Case of Reticulate Evolution in the Northeastern and Eastern Central Alps |
Q90350357 | Geographic distributions, phenotypes, and phylogenetic relationships of Phalloceros (Cyprinodontiformes: Poeciliidae): Insights about diversification among sympatric species pools |
Q111629827 | Geographical vs. ecological diversification in Carex section Phacocystis (Cyperaceae): Patterns hidden behind a twisted taxonomy |
Q31124509 | Geological and climatic forces driving speciation in the continentally distributed trilling chorus frogs (Pseudacris). |
Q33283006 | Geological dates and molecular rates: rapid divergence of rivers and their biotas |
Q22162503 | Geologically ancient DNA: fact or artefact? |
Q64931523 | Global Rate Variation in Bony Vertebrates. |
Q35225196 | Global biogeography of Alnus-associated Frankia actinobacteria |
Q28651722 | Global biogeography of scaly tree ferns (Cyatheaceae): evidence for Gondwanan vicariance and limited transoceanic dispersal |
Q28706228 | Global ecological pattern of ammonia-oxidizing archaea |
Q39295972 | Global history of the ancient monocot family Araceae inferred with models accounting for past continental positions and previous ranges based on fossils |
Q28763734 | Global patterns of diversification in the history of modern amphibians |
Q46212494 | Global patterns of leaf defenses in oak species |
Q63616761 | Global predictors of alien plant establishment success: combining niche and trait proxies |
Q28732233 | Gone with the plate: the opening of the Western Mediterranean basin drove the diversification of ground-dweller spiders |
Q51955260 | Gymnosperms on the EDGE. |
Q57038767 | Habitat fragmentation and genetic variability of tetrapod populations |
Q28749633 | Have giant lobelias evolved several times independently? Life form shifts and historical biogeography of the cosmopolitan and highly diverse subfamily Lobelioideae (Campanulaceae) |
Q33675296 | Heterogeneous molecular processes among the causes of how sequence similarity scores can fail to recapitulate phylogeny |
Q28749009 | Hidden levels of phylodiversity in Antarctic green algae: further evidence for the existence of glacial refugia |
Q33301039 | High variation and strong phylogeographic pattern among cpDNA haplotypes in Taxus wallichiana (Taxaceae) in China and North Vietnam. |
Q21089897 | Higher level phylogeny and the first divergence time estimation of Heteroptera (Insecta: Hemiptera) based on multiple genes |
Q54086228 | Higher-level metazoan relationships: recent progress and remaining questions |
Q28184490 | Higher-level systematics of rodents and divergence time estimates based on two congruent nuclear genes |
Q28764869 | Historical biogeography of two cosmopolitan families of flowering plants: Annonaceae and Rhamnaceae |
Q28764914 | Historical climate change and speciation: neotropical seasonally dry forest plants show patterns of both tertiary and quaternary diversification |
Q28710564 | Hornwort pyrenoids, carbon-concentrating structures, evolved and were lost at least five times during the last 100 million years |
Q28744634 | Host shifts and evolutionary radiations of butterflies |
Q33577316 | Host-associated genetic differentiation in a seed parasitic weevil Rhinusa antirrhini (Coleptera: Curculionidae) revealed by mitochondrial and nuclear sequence data |
Q44239378 | Host-symbiont stability and fast evolutionary rates in an ant-bacterium association: cospeciation of camponotus species and their endosymbionts, candidatus blochmannia |
Q33540166 | How accurate and robust are the phylogenetic estimates of Austronesian language relationships? |
Q34582699 | How and when did Old World ratsnakes disperse into the New World? |
Q35493111 | How do alien plants fit in the space-phylogeny matrix? |
Q36260502 | How the Aridification of Australia Structured the Biogeography and Influenced the Diversification of a Large Lineage of Australian Cicadas |
Q28710489 | How to handle speciose clades? Mass taxon-sampling as a strategy towards illuminating the natural history of Campanula (Campanuloideae) |
Q45330563 | Hybridization, mitochondrial DNA phylogeography, and prediction of the early stages of reproductive isolation: lessons from New Zealand cicadas (genus Kikihia). |
Q28752668 | Impact of duplicate gene copies on phylogenetic analysis and divergence time estimates in butterflies |
Q38928215 | Impact of gene family evolutionary histories on phylogenetic species tree inference by gene tree parsimony |
Q33624788 | Including secondary structure, fossils and molecular dating in the centipede tree of life |
Q35642382 | Incompatible Ages for Clearwing Butterflies Based on Alternative Secondary Calibrations |
Q44354410 | Incorporating parasite systematics in comparative analyses of variation in spleen mass and testes sizes of rodents |
Q56636709 | Incorporating phylogenetic uncertainty on phylogeny-based palaeontological dating and the timing of turtle diversification |
Q21092760 | Independently evolving species in asexual bdelloid rotifers |
Q30797551 | Inference of a radiation in Mastus (Gastropoda, Pulmonata, Enidae) on the island of Crete |
Q31009923 | Inflation of Molecular Clock Rates and Dates: Molecular Phylogenetics, Biogeography, and Diversification of a Global Cicada Radiation from Australasia (Hemiptera: Cicadidae: Cicadettini). |
Q21283984 | Influence of Tertiary paleoenvironmental changes on the diversification of South American mammals: a relaxed molecular clock study within xenarthrans |
Q30823492 | Infrequent and unidirectional colonization of hyperdiverse Papuadytes diving beetles in New Caledonia and New Guinea |
Q60949419 | Insights into the Evolution of the New World Diploid Cottons (Gossypium, Subgenus Houzingenia) Based on Genome Sequencing |
Q21089904 | Insights into the ecology and evolutionary success of crocodilians revealed through bite-force and tooth-pressure experimentation |
Q36649867 | Insights into the historical construction of species-rich biomes from dated plant phylogenies, neutral ecological theory and phylogenetic community structure |
Q31155010 | Integrating coalescent and phylogenetic approaches to delimit species in the lichen photobiont Trebouxia. |
Q56480816 | Integrating phylogeny, molecular clocks, and the fossil record in the evolution of coralline algae (Corallinales and Sporolithales, Rhodophyta) |
Q34378834 | Integrating reptilian herpesviruses into the family herpesviridae |
Q21093621 | Integration of molecules and new fossils supports a Triassic origin for Lepidosauria (lizards, snakes, and tuatara) |
Q59330302 | Integration of phylogenomics and molecular modeling reveals lineage-specific diversification of toxins in scorpions |
Q33240218 | Intercontinental biogeography of subfamily Orontioideae (Symplocarpus, Lysichiton, and Orontium) of Araceae in Eastern Asia and North America |
Q47247110 | Internal consistency as a method to assess the quality of dating estimates using multiple markers. |
Q34230475 | Interplay between oxygen and Fe-S cluster biogenesis: insights from the Suf pathway |
Q54787230 | Interspecific delimitation and phylogenetic origin of Pugionium (Brassicaceae) |
Q46604283 | Intraspecific variability and timing in ancestral ecology reconstruction: a test case from the cape flora |
Q28764829 | Introduction and synthesis: Plant phylogeny and the origin of major biomes |
Q59159182 | Intron evolution in a phylogenetic perspective: Divergent trends in the two copies of the duplicateddefgene inImpatiensL. (Balsaminaceae) |
Q91829025 | Is dispersal mode a driver of diversification and geographical distribution in the tropical plant family Melastomataceae? |
Q38404852 | Karyotypic changes through dysploidy persist longer over evolutionary time than polyploid changes |
Q42034202 | Karyotypic diversity and speciation in Agrodiaetus butterflies |
Q51144949 | Key questions and challenges in angiosperm macroevolution. |
Q45722103 | Landscape genetic patterns of the rainbow darter Etheostoma caeruleum: a catchment analysis of mitochondrial DNA sequences and nuclear microsatellites. |
Q37847750 | Language evolution and human history: what a difference a date makes |
Q64013335 | Large-scale molecular phylogeny, morphology, divergence-time estimation, and the fossil record of advanced caenophidian snakes (Squamata: Serpentes) |
Q45740213 | Large-scale patterns of diversification in the widespread legume genus Senna and the evolutionary role of extrafloral nectaries |
Q110697235 | Large-scale phylogenomics of the genus Macrostomum (Platyhelminthes) reveals cryptic diversity and novel sexual traits |
Q28763986 | Late Cretaceous vicariance in Gondwanan amphibians |
Q30051479 | Lineage divergence of a freshwater snail clade associated with post-Tethys marine basin development |
Q90015638 | Local and relaxed clocks: the best of both worlds |
Q34303980 | Local molecular clocks in three nuclear genes: divergence times for rodents and other mammals and incompatibility among fossil calibrations |
Q34159872 | Loss of flight promotes beetle diversification |
Q24547650 | Low genetic variation and no detectable population structure in aspergillus fumigatus compared to closely related Neosartorya species |
Q28710442 | Low rates of lateral gene transfer among metabolic genes define the evolving biogeochemical niches of archaea through deep time |
Q101632489 | Lygosomine phylogeny and the origins of Australian scincid lizards |
Q56975237 | Macroecology meets macroevolution: evolutionary niche dynamics in the seaweedHalimeda |
Q28602526 | Madagascar's grasses and grasslands: anthropogenic or natural? |
Q24657281 | Major evolutionary transitions in ant agriculture |
Q34777890 | Major histocompatibility complex class I evolution in songbirds: universal primers, rapid evolution and base compositional shifts in exon 3 |
Q36877395 | Mammalian evolution and biomedicine: new views from phylogeny |
Q59128410 | Manipulating plant phylogenetic diversity for green roof ecosystem service delivery |
Q33998387 | Mass extinction, gradual cooling, or rapid radiation? Reconstructing the spatiotemporal evolution of the ancient angiosperm genus Hedyosmum (Chloranthaceae) using empirical and simulated approaches |
Q21090254 | Mastacembelid eels support Lake Tanganyika as an evolutionary hotspot of diversification |
Q56384888 | Measurably evolving populations |
Q52924854 | Mechanical sensitivity and the dynamics of evolutionary rate shifts in biomechanical systems. |
Q36083684 | Mechanistic model of evolutionary rate variation en route to a nonphotosynthetic lifestyle in plants. |
Q67212840 | Megaphylogeny resolves global patterns of mushroom evolution |
Q28764858 | Metacommunity process rather than continental tectonic history better explains geographically structured phylogenies in legumes |
Q96179568 | Microcnemum coralloides (Chenopodiaceae- Salicornioideae): an example of intraspecific East-West disjunctions in the Mediterranean region |
Q47289458 | Mid-Tertiary dispersal, not Gondwanan vicariance explains distribution patterns in the wax palm subfamily (Ceroxyloideae: Arecaceae). |
Q104454945 | Millipede assassins and allies (Heteroptera: Reduviidae: Ectrichodiinae, Tribelocephalinae): total evidence phylogeny, revised classification and evolution of sexual dimorphism |
Q33857350 | Missing data in phylogenetic analysis: reconciling results from simulations and empirical data |
Q30876465 | Mitochondrial DNA phylogeography and population history of Meladema diving beetles on the Atlantic Islands and in the Mediterranean basin (Coleoptera, Dytiscidae). |
Q21283953 | Mitochondrial phylogeny and phylogeography of East African squeaker catfishes (Siluriformes: Synodontis) |
Q44273960 | Mitochondrial phylogeography of New Zealand freshwater crayfishes, Paranephrops spp. |
Q33582622 | Mitochondrial substitution rates are extraordinarily elevated and variable in a genus of flowering plants |
Q34007359 | Mitogenomic analyses of caniform relationships |
Q34457769 | Mitogenomic analyses place the gharial (Gavialis gangeticus) on the crocodile tree and provide pre-K/T divergence times for most crocodilians |
Q37425940 | Modeling extinction risk of endemic birds of mainland china |
Q41758840 | Modularized evolution in archaeal methanogens phylogenetic forest |
Q98225272 | Molecular Evaluation of the Fairy Shrimp Family Branchinectidae (Crustacea: Anostraca) Supports Peripatric Speciation and Complex Divergence Patterns |
Q55755642 | Molecular Phylogenetics and Biogeography of the Caribbean-Centered Croton Subgenus Moacroton (Euphorbiaceae s.s.) |
Q21090986 | Molecular and phenotypic evidence of a new species of genus Esox (Esocidae, Esociformes, Actinopterygii): the southern pike, Esox flaviae |
Q47363050 | Molecular architecture and rates of DNA substitutions of the mitochondrial control region of cracid birds |
Q35685501 | Molecular clocks and explosive radiations |
Q42657413 | Molecular clocks and geological dates: cytochrome b of Anolis extremus substantially contradicts dating of Barbados emergence |
Q28607312 | Molecular clocks and the early evolution of metazoan nervous systems |
Q54555079 | Molecular data resolves relationships within Heteroceridae (Coleoptera: Dryopoidea) |
Q51965446 | Molecular dates for the "cambrian explosion": the influence of prior assumptions. |
Q47271449 | Molecular dating and biogeography of fig-pollinating wasps |
Q21283961 | Molecular dating of caprines using ancient DNA sequences of Myotragus balearicus, an extinct endemic Balearic mammal |
Q34604991 | Molecular dating of phylogenies by likelihood methods: a comparison of models and a new information criterion |
Q29042433 | Molecular dating of the ‘Gondwanan’ plant family Proteaceae is only partially congruent with the timing of the break-up of Gondwana |
Q47384392 | Molecular estimation of eulipotyphlan divergence times and the evolution of "Insectivora". |
Q48075325 | Molecular evidence for a rapid late-Miocene radiation of Australasian venomous snakes (Elapidae, Colubroidea). |
Q43944462 | Molecular evidence for broad-scale distributions in bdelloid rotifers: everything is not everywhere but most things are very widespread |
Q39266009 | Molecular evidence for the age, origin, and evolutionary history of the American desert plant genus Tiquilia (Boraginaceae). |
Q28775831 | Molecular evidence links cryptic diversification in polar planktonic protists to Quaternary climate dynamics |
Q47305789 | Molecular phylogenetic dating of asterid flowering plants shows early Cretaceous diversification |
Q51974560 | Molecular phylogenetics and biogeography of Neotropical piping guans (Aves: Galliformes): Pipile Bonaparte, 1856 is synonym of Aburria Reichenbach, 1853. |
Q28658795 | Molecular phylogenetics and temporal diversification in the genus Aeromonas based on the sequences of five housekeeping genes |
Q43863231 | Molecular phylogenetics of shrews (Mammalia: Soricidae) reveal timing of transcontinental colonizations |
Q110451177 | Molecular phylogenetics of sub-Saharan African natricine snakes, and the biogeographic origins of the Seychelles endemic Lycognathophis seychellensis |
Q28301872 | Molecular phylogenetics of the Gloeophyllales and relative ages of clades of Agaricomycotina producing a brown rot |
Q38883708 | Molecular phylogenetics of the Ronnbergia Alliance (Bromeliaceae, Bromelioideae) and insights into their morphological evolution. |
Q28236239 | Molecular phylogenetics of the butterflyfishes (Chaetodontidae): taxonomy and biogeography of a global coral reef fish family |
Q28755727 | Molecular phylogenetics reveal multiple tertiary vicariance origins of the African rain forest trees |
Q33347390 | Molecular phylogenies and historical biogeography of a circumtropical group of gastropods (Genus: Nerita): implications for regional diversity patterns in the marine tropics |
Q47264782 | Molecular phylogeny and biogeography of Pseudotsuga (Pinaceae): insights into the floristic relationship between Taiwan and its adjacent areas. |
Q40270520 | Molecular phylogeny and biogeography of an ancient Holarctic lineage of mygalomorph spiders (Araneae: Antrodiaetidae: Antrodiaetus). |
Q21385694 | Molecular phylogeny and biogeography of the Cuban genus Girardinus Poey, 1854 and relationships within the tribe Girardinini (Actinopterygii, Poeciliidae). |
Q53126754 | Molecular phylogeny and biogeography of the Neotropical cichlid fish tribe Cichlasomatini (Teleostei: Cichlidae: Cichlasomatinae). |
Q47199323 | Molecular phylogeny and dating of Asteliaceae (Asparagales): Astelia s.l. evolution provides insight into the Oligocene history of New Zealand |
Q44655351 | Molecular phylogeny and historical biogeography of the land snail genus Solatopupa (Pulmonata) in the peri-Tyrrhenian area |
Q47222014 | Molecular phylogeny and intra- and intercontinental biogeography of Calycanthaceae |
Q28282003 | Molecular phylogeny and node time estimation of bioluminescent Lantern Sharks (Elasmobranchii: Etmopteridae) |
Q54555232 | Molecular phylogeny of Pacific Island Colymbetinae: radiation of New Caledonian and Fijian species (Coleoptera, Dytiscidae) |
Q21284028 | Molecular phylogeny of microhylid frogs (Anura: Microhylidae) with emphasis on relationships among New World genera |
Q28757488 | Molecular phylogeny of the Drosophila obscura species group, with emphasis on the Old World species |
Q51860469 | Molecular phylogeny of the genus Pseudoplatystoma (Bleeker, 1862): biogeographic and evolutionary implications. |
Q39909301 | Molecular phylogeny of the small carpenter bees (Hymenoptera: Apidae: Ceratinini) indicates early and rapid global dispersal |
Q28742212 | Molecular phylogeny of the subgenus Ceratotropis (genus Vigna, Leguminosae) reveals three eco-geographical groups and Late Pliocene-Pleistocene diversification: evidence from four plastid DNA region sequences |
Q28648313 | Molecular phylogeny reveals high diversity, geographic structure and limited ranges in neotenic net-winged beetles platerodrilus (coleoptera: lycidae) |
Q42044428 | Molecular phylogeny, historical biogeography, and divergence time estimates for swallowtail butterflies of the genus Papilio (Lepidoptera: Papilionidae). |
Q41465677 | Molecular phylogeography reveals island colonization history and diversification of western Indian Ocean sunbirds (Nectarinia: Nectariniidae). |
Q46879713 | Molecular systematics and biogeography of Logania R.Br. (Loganiaceae). |
Q33200885 | Molecular systematics of Salmonidae: combined nuclear data yields a robust phylogeny |
Q33538756 | Molecular systematics: A synthesis of the common methods and the state of knowledge |
Q38257608 | Molecular-clock methods for estimating evolutionary rates and timescales |
Q24653740 | Molecules, morphology, and ecology indicate a recent, amphibious ancestry for echidnas |
Q28751193 | Monophyly of terrestrial adephagan beetles as indicated by three nuclear genes (Coleoptera: Carabidae and Trachypachidae) |
Q30051485 | Morphology, molecular phylogeny, and taxonomic inconsistencies in the study ofBradypussloths (Pilosa: Bradypodidae) |
Q45892372 | Multilocus analyses of an Antarctic fish species flock (Teleostei, Notothenioidei, Trematominae): phylogenetic approach and test of the early-radiation event |
Q33270523 | Multilocus genealogies reveal multiple cryptic species and biogeographical complexity in the California turret spider Antrodiaetus riversi (Mygalomorphae, Antrodiaetidae). |
Q28764837 | Multiple Miocene Melastomataceae dispersal between Madagascar, Africa and India |
Q28597678 | Multiple Polyploidization Events across Asteraceae with Two Nested Events in the Early History Revealed by Nuclear Phylogenomics |
Q28756334 | Multiple ancient origins of neoteny in Lycidae(Coleoptera): consequences for ecology and macroevolution |
Q24676802 | Multiple gene evidence for expansion of extant penguins out of Antarctica due to global cooling |
Q36259453 | Multiple measures could alleviate long-branch attraction in phylogenomic reconstruction of Cupressoideae (Cupressaceae). |
Q28768106 | Multiple mechanisms promote the retained expression of gene duplicates in the tetraploid frog Xenopus laevis |
Q38632274 | Mutation predicts 40 million years of fly wing evolution. |
Q28768534 | Naked corals: skeleton loss in Scleractinia |
Q41443922 | Neoendemism in Madagascan scaly tree ferns results from recent, coincident diversification bursts |
Q44197149 | Neotropical mutualism between Acacia and Pseudomyrmex: phylogeny and divergence times |
Q30440287 | Neutral theory, phylogenies, and the relationship between phenotypic change and evolutionary rates |
Q51629171 | New heuristic methods for joint species delimitation and species tree inference. |
Q57898440 | New phylogenetic hypotheses for the core Chlorophyta based on chloroplast sequence data |
Q28681692 | Next-generation museomics disentangles one of the largest primate radiations |
Q67244128 | Next-generation museum genomics: Phylogenetic relationships among palpimanoid spiders using sequence capture techniques (Araneae: Palpimanoidea) |
Q34815066 | Niche conservatism constrains Australian honeyeater assemblages in stressful environments |
Q44022175 | Niche evolution and adaptive radiation: testing the order of trait divergence |
Q57585279 | Noise and biases in genomic data may underlie radically different hypotheses for the position of Iguania within Squamata |
Q34674529 | Nonuniform processes of chromosome evolution in sedges (Carex: Cyperaceae). |
Q35911509 | Not going with the flow: a comprehensive time-calibrated phylogeny of dragonflies (Anisoptera: Odonata: Insecta) provides evidence for the role of lentic habitats on diversification |
Q46884468 | Not only for egg yolk--functional and evolutionary insights from expression, selection, and structural analyses of Formica ant vitellogenins. |
Q30838201 | Novel non-parametric models to estimate evolutionary rates and divergence times from heterochronous sequence data. |
Q42154275 | Nuclear and mitochondrial sequences confirm complex colonization patterns and clear species boundaries for flightless weevils in the Galápagos archipelago |
Q91792264 | Nuclear and plastid DNA phylogeny of tribe Cardueae (Compositae) with Hyb-Seq data: A new subtribal classification and a temporal diversification framework |
Q46049880 | Nuclear gene phylogeography reveals the historical legacy of an ancient inland sea on lineages of the western pond turtle, Emys marmorata in California |
Q44416006 | Nuclear ribosomal DNA and karyotypes indicate a NW African origin of South American Hypochaeris (Asteraceae, Cichorieae). |
Q45072336 | Nucleotide substitution rates for the full set of mitochondrial protein-coding genes in Coleoptera |
Q33933014 | On the accuracy of language trees |
Q28655429 | On the age of eukaryotes: evaluating evidence from fossils and molecular clocks |
Q36255641 | Ongoing Speciation and Gene Flow between Taxonomically Challenging Trochulus Species Complex (Gastropoda: Hygromiidae). |
Q28960191 | Origin and Relationships of the Austral Genus Abrotanella (Asteraceae) Inferred from DNA Sequences |
Q33328148 | Origin and diversification of the Greater Cape flora: ancient species repository, hot-bed of recent radiation, or both? |
Q39894708 | Origin and early evolution of photosynthetic eukaryotes in freshwater environments: reinterpreting proterozoic paleobiology and biogeochemical processes in light of trait evolution |
Q92317603 | Origin and evolution of the genus Piper in Peninsular India |
Q24648292 | Origin, adaptive radiation and diversification of the Hawaiian lobeliads (Asterales: Campanulaceae) |
Q99975701 | Origins and diversification of Indo-West Pacific marine fauna: evolutionary history and biogeography of turban shells (Gastropoda, Turbinidae) |
Q30350457 | Origins of host-specific populations of the blast pathogen Magnaporthe oryzae in crop domestication with subsequent expansion of pandemic clones on rice and weeds of rice. |
Q34618988 | Origins of social parasitism: the importance of divergence ages in phylogenetic studies |
Q21283970 | Out of Tanganyika: genesis, explosive speciation, key-innovations and phylogeography of the haplochromine cichlid fishes |
Q42031935 | Out-of-Africa origin and dispersal-mediated diversification of the butterfly genus Junonia (Nymphalidae: Nymphalinae). |
Q57069626 | PHYLOGENETIC ANALYSES REVEAL UNEXPECTED PATTERNS IN THE EVOLUTION OF REPRODUCTIVE MODES IN FROGS |
Q99637278 | Palaeoclimate ocean conditions shaped the evolution of corals and their skeletons through deep time |
Q34985558 | Pan-vertebrate comparative genomics unmasks retrovirus macroevolution |
Q42063452 | Parallel Evolution and Horizontal Gene Transfer of the pst Operon in Firmicutes from Oligotrophic Environments. |
Q28756403 | Pattern and timing of diversification in Yucca (Agavaceae): specialized pollination does not escalate rates of diversification |
Q45016634 | Patterns and processes in the genetic differentiation of the Brachionus calyciflorus complex, a passively dispersing freshwater zooplankton |
Q28764852 | Patterns in the assembly of temperate forests around the Northern Hemisphere |
Q39947348 | Patterns of diversification and ancestral range reconstruction in the southeast Asian-Pacific angiosperm lineage Cyrtandra (Gesneriaceae). |
Q51527927 | Patterns of mammalian diversification in recent evolutionary times: global tendencies and methodological issues. |
Q33526705 | Peatmoss (Sphagnum) diversification associated with Miocene Northern Hemisphere climatic cooling? |
Q57077595 | Phylogenetic Hypothesis Testing |
Q28960145 | Phylogenetic Relationships and Biogeography of Ranunculus and Allied Genera (Ranunculaceae) in the Mediterranean Region and in the European Alpine System |
Q28754609 | Phylogenetic analyses: A toolbox expanding towards Bayesian methods |
Q47282105 | Phylogenetic analysis informed by geological history supports multiple, sequential invasions of the Mediterranean Basin by the angiosperm family Araceae |
Q57568122 | Phylogenetic analysis of 1.5 Mbp and platypus EST data refute the Marsupionta hypothesis and unequivocally support Monotremata as sister group to Marsupialia/Placentalia |
Q28279563 | Phylogenetic analysis of Hordeum (Poaceae) as inferred by nuclear rDNA ITS sequences |
Q21562349 | Phylogenetic analysis of seven WRKY genes across the palm subtribe Attaleinae (Arecaceae) [corrected] identifies Syagrus as sister group of the coconut |
Q33254631 | Phylogenetic analysis of the evolution of the niche in lizards of the Anolis sagrei group |
Q31162300 | Phylogenetic and biogeographic complexity of Magnoliaceae in the Northern Hemisphere inferred from three nuclear data sets |
Q33208651 | Phylogenetic and biogeographic diversification of Rhus (Anacardiaceae) in the Northern Hemisphere |
Q34215082 | Phylogenetic and epidemic modeling of rapidly evolving infectious diseases |
Q35948379 | Phylogenetic classification of yeasts and related taxa within Pucciniomycotina |
Q33703375 | Phylogenetic climatic niche conservatism and evolution of climatic suitability in Neotropical Angraecinae (Vandeae, Orchidaceae) and their closest African relatives. |
Q37801983 | Phylogenetic comparative approaches for studying niche conservatism. |
Q31111097 | Phylogenetic conservatism and climate factors shape flowering phenology in alpine meadows |
Q39584555 | Phylogenetic dispersion of host use in a tropical insect herbivore community |
Q48323029 | Phylogenetic estimates of diversification rate are affected by molecular rate variation. |
Q38447908 | Phylogenetic evidence for a major reversal of life-history evolution in plethodontid salamanders |
Q47204656 | Phylogenetic evidence for competitively driven divergence: body-size evolution in Caribbean treefrogs (Hylidae: Osteopilus). |
Q28756258 | Phylogenetic history underlies elevational biodiversity patterns in tropical salamanders |
Q33499058 | Phylogenetic origin of Phyllolobium with a further implication for diversification of Astragalus in China |
Q28749366 | Phylogenetic origins of the Himalayan endemic Dolomiaea, Diplazoptilon and Xanthopappus (Asteraceae: Cardueae) based on three DNA regions |
Q54494805 | Phylogenetic patterns and diversification in the caesalpinioid legumesThis paper is one of a selection of papers published in the Special Issue on Systematics Research. |
Q21192752 | Phylogenetic position of a whale-fall lancelet (Cephalochordata) inferred from whole mitochondrial genome sequences |
Q55693108 | Phylogenetic prediction of the maximum per capita rate of population growth. |
Q29393179 | Phylogenetic reconstruction and shell evolution of the Diplommatinidae (Gastropoda: Caenogastropoda) |
Q46821253 | Phylogenetic relationships and divergence time estimate of African anguilliform catfish (Siluriformes: Clariidae) inferred from ribosomal gene and spacer sequences |
Q28728443 | Phylogenetic relationships and the evolution of regulatory gene sequences in the parrotfishes |
Q54539685 | Phylogenetic relationships of Dalyat mirabilis Mateu, 2002, with a revised molecular phylogeny of ground beetles (Coleoptera, Carabidae) |
Q43537336 | Phylogenetic relationships of Loxosceles and Sicarius spiders are consistent with Western Gondwanan vicariance |
Q47263596 | Phylogenetic relationships, divergence time estimation, and global biogeographic patterns of calopterygoid damselflies (odonata, zygoptera) inferred from ribosomal DNA sequences |
Q29041581 | Phylogenetic relationships, diversification and biogeography in NeotropicalBrotogerisparakeets |
Q39605794 | Phylogenetic signal in diatom ecology: perspectives for aquatic ecosystems biomonitoring |
Q29028803 | Phylogenetic systematics and tempo of evolution of the Viverrinae (Mammalia, Carnivora, Viverridae) within feliformians: Implications for faunal exchanges between Asia and Africa |
Q111629084 | Phylogenetics and biogeography of eastern Asian-North American disjunct genus Pachysandra (Buxaceae) inferred from nucleotide sequences |
Q21093416 | Phylogenetics of Cucumis (Cucurbitaceae): cucumber (C. sativus) belongs in an Asian/Australian clade far from melon (C. melo) |
Q99656999 | Phylogenetics of modern shorebirds (Charadriiformes) based on phenotypic evidence: analysis and discussion |
Q34239632 | Phylogenetics of the millipede genus Brachycybe Wood, 1864 (Diplopoda: Platydesmida: Andrognathidae): patterns of deep evolutionary history and recent speciation |
Q55871724 | Phylogenetics, divergence times and diversification from three genomic partitions in monocots |
Q47254487 | Phylogenetics, species boundaries and timing of resource tracking in a highly specialized group of seed beetles (Coleoptera: Chrysomelidae: Bruchinae). |
Q110697325 | Phylogenomic analysis, reclassification, and evolution of South American nemesioid burrowing mygalomorph spiders |
Q33556679 | Phylogenomics and the dynamic genome evolution of the genus Streptococcus. |
Q44868828 | Phylogeny and Bayesian divergence time estimations of small-headed flies (Diptera: Acroceridae) using multiple molecular markers |
Q28293911 | Phylogeny and biogeography of Altingiaceae: evidence from combined analysis of five non-coding chloroplast regions |
Q28757190 | Phylogeny and biogeography of Cedrus (Pinaceae) inferred from sequences of seven paternal chloroplast and maternal mitochondrial DNA regions |
Q31054642 | Phylogeny and biogeography of Croton alabamensis (Euphorbiaceae), a rare shrub from Texas and Alabama, using DNA sequence and AFLP data |
Q54557176 | Phylogeny and biogeography of Sassafras (Lauraceae) disjunct between eastern Asia and eastern North America |
Q39620047 | Phylogeny and biogeography of exacum (gentianaceae): a disjunctive distribution in the Indian ocean basin resulted from long distance dispersal and extensive radiation |
Q48693138 | Phylogeny and biogeography of the alpine newt Mesotriton alpestris (Salamandridae, Caudata), inferred from mtDNA sequences |
Q28282403 | Phylogeny and divergence-date estimates of rapid radiations in muroid rodents based on multiple nuclear genes |
Q54521626 | Phylogeny and diversification of diving beetles (Coleoptera: Dytiscidae) |
Q24563351 | Phylogeny and diversification of the largest avian radiation |
Q47281160 | Phylogeny and evolutionary history of the blister beetles (Coleoptera, Meloidae). |
Q42012569 | Phylogeny and evolutionary history of the silkworm |
Q46871190 | Phylogeny and forelimb disparity in waterbirds |
Q110697361 | Phylogeny and secondary sexual trait evolution in Schizocosa wolf spiders (Araneae, Lycosidae) shows evidence for multiple gains and losses of ornamentation and species delimitation uncertainty |
Q33257497 | Phylogeny and temporal diversification of Calomys (Rodentia, Sigmodontinae): implications for the biogeography of an endemic genus of the open/dry biomes of South America |
Q33966732 | Phylogeny and temporal diversification of darters (Percidae: Etheostomatinae). |
Q116205948 | Phylogeny of Australasian agamid lizards based on nuclear and mitochondrial genes: implications for morphological evolution and biogeography |
Q33251061 | Phylogeny of Chaetanthera (Asteraceae: Mutisieae) reveals both ancient and recent origins of the high elevation lineages |
Q28265426 | Phylogeny of Dictyoptera: Dating the Origin of Cockroaches, Praying Mantises and Termites with Molecular Data and Controlled Fossil Evidence |
Q28598220 | Phylogeny of Elatinaceae and the Tropical Gondwanan Origin of the Centroplacaceae(Malpighiaceae, Elatinaceae) Clade |
Q111741553 | Phylogeny of Marsdenieae (Apocynaceae, Asclepiadoideae) based on chloroplast and nuclear loci, with a conspectus of the genera |
Q22945802 | Phylogeny of Opuntia s.s. (Cactaceae): Clade delineation, geographic origins, and reticulate evolution |
Q33314190 | Phylogeny of Paramysis (Crustacea: Mysida) and the origin of Ponto-Caspian endemic diversity: resolving power from nuclear protein-coding genes |
Q28960294 | Phylogeny of Salicornioideae (Chenopodiaceae): Diversification, Biogeography, and Evolutionary Trends in Leaf and Flower Morphology |
Q31115141 | Phylogeny of extant and fossil Juglandaceae inferred from the integration of molecular and morphological data sets |
Q44117746 | Phylogeny of iguanian lizards inferred from 29 nuclear loci, and a comparison of concatenated and species-tree approaches for an ancient, rapid radiation |
Q59116331 | Phylogeny, biogeography and classification of the snake superfamily Elapoidea: a rapid radiation in the late Eocene |
Q42019472 | Phylogeny, biogeography, and host-plant association in the subfamily Apaturinae (Insecta: Lepidoptera: Nymphalidae) inferred from eight nuclear and seven mitochondrial genes. |
Q51721501 | Phylogeny, divergence-time estimation, biogeography and social parasite-host relationships of the Holarctic ant genus Myrmica (Hymenoptera: Formicidae). |
Q44015674 | Phylogeny, diversification rates and species boundaries of Mesoamerican firs (Abies, Pinaceae) in a genus-wide context |
Q28768918 | Phylogeny, evolution, and biogeography of Asiatic Salamanders (Hynobiidae) |
Q47211121 | Phylogeny, historical biogeography, and patterns of diversification for Pinus (Pinaceae): phylogenetic tests of fossil-based hypotheses |
Q35759962 | Phylogeny, species delimitation and convergence in the South American bothriurid scorpion genus Brachistosternus Pocock 1893: Integrating morphology, nuclear and mitochondrial DNA. |
Q54555400 | Phylogeographic analysis of Pimoidae (Arachnida: Araneae) inferred from mitochondrial cytochrome c oxidase subunit I and nuclear 28S rRNA gene regions |
Q39172277 | Phylogeography and bindin evolution in Arbacia, a sea urchin genus with an unusual distribution. |
Q34249345 | Phylogeography of Rift Valley Fever virus in Africa reveals multiple introductions in Senegal and Mauritania |
Q30814554 | Phylogeography of a subterranean amphipod reveals cryptic diversity and dynamic evolution in extreme environments. |
Q39031789 | Phylogeography of the Bothrops jararaca complex (Serpentes: Viperidae): past fragmentation and island colonization in the Brazilian Atlantic Forest |
Q39145586 | Phylogeography of the ocellated skink Chalcides ocellatus (Squamata, Scincidae), with the use of mtDNA sequences: a hitch-hiker's guide to the Mediterranean |
Q47302047 | Phylogeography of two European newt species--discordance between mtDNA and morphology |
Q46246935 | Physalis and physaloids: A recent and complex evolutionary history |
Q33997312 | Pinniped phylogeny and a new hypothesis for their origin and dispersal |
Q90721282 | Placing the regionally threatened moss Orthodontium gracile in the big picture - Phylogeny, genome incongruence and anthropogenic dispersal in the order Orthodontiales |
Q28754782 | Plants with double genomes might have had a better chance to survive the Cretaceous-Tertiary extinction event |
Q57227855 | Pliocene forest dynamics as a primary driver of African bird speciation |
Q43639266 | Plumage evolution in relation to light environment in a novel clade of Neotropical tanagers |
Q64233586 | Population genetic structure and geographical variation in Neotricula aperta (Gastropoda: Pomatiopsidae), the snail intermediate host of Schistosoma mekongi (Digenea: Schistosomatidae) |
Q28756016 | Prehistorical climate change increased diversification of a group of butterflies |
Q28742193 | Primate extinction risk and historical patterns of speciation and extinction in relation to body mass |
Q57237215 | Processes driving male breeding colour and ecomorphological diversification in rainbow skinks: a phylogenetic comparative test |
Q24645517 | Progressive island colonization and ancient origin of Hawaiian Metrosideros (Myrtaceae) |
Q28654446 | Prospects for building large timetrees using molecular data with incomplete gene coverage among species |
Q46671923 | Puzzling rocks and complicated clocks: how to optimize molecular dating approaches in historical phytogeography |
Q24600564 | Quantitative prediction of molecular clock and ka/ks at short timescales |
Q28185340 | RAG-1 sequences resolve phylogenetic relationships within Charadriiform birds |
Q57077581 | RAPID CLADOGENESIS IN MARINE FISHES REVISITED |
Q88874864 | REPLICATE PATTERNS OF SPECIES RICHNESS, HISTORICAL BIOGEOGRAPHY, AND PHYLOGENY IN HOLARCTIC TREEFROGS |
Q28284327 | Radiation of extant cetaceans driven by restructuring of the oceans |
Q42458220 | Radiation of extant marsupials after the K/T boundary: evidence from complete mitochondrial genomes |
Q28764843 | Radiation of the Australian flora: what can comparisons of molecular phylogenies across multiple taxa tell us about the evolution of diversity in present-day communities? |
Q38932785 | Radiation, multiple dispersal and parallelism in the skinks, Chalcides and Sphenops (Squamata: Scincidae), with comments on Scincus and Scincopus and the age of the Sahara Desert. |
Q44358738 | Rampant host- and defensive phenotype-associated diversification in a goldenrod gall midge. |
Q28709533 | Rapid and recent world-wide diversification of bluegrasses (Poa, Poaceae) and related genera |
Q21283874 | Rapid and repeated limb loss in a clade of scincid lizards |
Q33270876 | Rapid diversification, incomplete isolation, and the "speciation clock" in North American salamanders (Genus Plethodon): testing the hybrid swarm hypothesis of rapid radiation |
Q56228231 | Rapid lineage accumulation in a non-adaptive radiation: phylogenetic analysis of diversification rates in eastern North American woodland salamanders (Plethodontidae: Plethodon) |
Q33435723 | Rapid radiation of Impatiens (Balsaminaceae) during Pliocene and Pleistocene: result of a global climate change. |
Q33338225 | Rates and patterns in the evolution of snake-like body form in squamate reptiles: evidence for repeated re-evolution of lost digits and long-term persistence of intermediate body forms |
Q46001605 | Rates of evolution of hybrid inviability in birds and mammals. |
Q29618961 | Rates of molecular evolution are linked to life history in flowering plants |
Q44874707 | Rates of nucleotide substitution in Cornaceae (Cornales)-Pattern of variation and underlying causal factors |
Q30641520 | Rates of speciation and morphological evolution are correlated across the largest vertebrate radiation. |
Q28236332 | Re-evolution of lost mandibular teeth in frogs after more than 200 million years, and re-evaluating Dollo's law |
Q28750326 | Reassessing the temporal evolution of orchids with new fossils and a Bayesian relaxed clock, with implications for the diversification of the rare South American genus Hoffmannseggella (Orchidaceae: Epidendroideae) |
Q28763130 | Recalibrated tree of leaf beetles (Chrysomelidae) indicates independent diversification of angiosperms and their insect herbivores |
Q28766871 | Recent and simultaneous origins of eusociality in halictid bees |
Q21283939 | Recent evolution of alternative reproductive modes in the 'living fossil' Triops cancriformis |
Q38948432 | Recent long-distance dispersal overshadows ancient biogeographical patterns in a pantropical angiosperm family (Simaroubaceae, Sapindales). |
Q28727186 | Recent progress in paleontological methods for dating the Tree of Life |
Q33996502 | Recently formed polyploid plants diversify at lower rates |
Q54546616 | Recognition of a species-poor, geographically restricted but morphologically diverse Cape lineage of diving beetles (Coleoptera: Dytiscidae: Hyphydrini) |
Q28744431 | Reconciling molecular phylogenies with the fossil record |
Q28703889 | Reconstructing the evolutionary history of transposable elements |
Q39408118 | Reconstructing the history of Campanulaceae with a Bayesian approach to molecular dating and dispersal-vicariance analyses. |
Q33355186 | Recurrent evolution of dioecy in bryophytes |
Q35721159 | Reduced mRNA secondary-structure stability near the start codon indicates functional genes in prokaryotes |
Q45912237 | Refugia, dispersal and divergence in a forest archipelago: a study of Streptocarpus in eastern South Africa. |
Q44892750 | Relationship between species co-occurrence and rate of morphological change in Percina darters (Percidae: Etheostomatinae). |
Q51562076 | Relative embryo length as an adaptation to habitat and life cycle in Apiaceae. |
Q51585209 | Relaxed clocks and inferences of heterogeneous patterns of nucleotide substitution and divergence time estimates across whales and dolphins (Mammalia: Cetacea). |
Q21146382 | Relaxed molecular clock provides evidence for long-distance dispersal of Nothofagus (southern beech) |
Q34019219 | Relaxed molecular clocks, the bias-variance trade-off, and the quality of phylogenetic inference |
Q21146068 | Relaxed phylogenetics and dating with confidence |
Q28604209 | Relaxing the Molecular Clock to Different Degrees for Different Substitution Types |
Q28750225 | Repeated climate-linked host shifts have promoted diversification in a temperate clade of leaf-mining flies |
Q46261942 | Repeated evolution and reversibility of self-fertilization in the volvocine green algae |
Q24678024 | Repeated evolution of net venation and fleshy fruits among monocots in shaded habitats confirms a priori predictions: evidence from an ndhF phylogeny |
Q28754889 | Repeated independent evolution of obligate pollination mutualism in the Phyllantheae-Epicephala association |
Q36028824 | Repeated invasions into the twilight zone: evolutionary origins of a novel assemblage of fishes from deep Caribbean reefs |
Q21134514 | Repeated origin and loss of adhesive toepads in geckos |
Q117478758 | Repeated parallel losses of inflexed stamens in Moraceae: Phylogenomics and generic revision of the tribe Moreae and the reinstatement of the tribe Olmedieae (Moraceae) |
Q57227893 | Repeated trans-Atlantic dispersal catalysed a global songbird radiation |
Q28602804 | Resolution of Brassicaceae Phylogeny Using Nuclear Genes Uncovers Nested Radiations and Supports Convergent Morphological Evolution |
Q34750162 | Resolving an ancient, rapid radiation in Saxifragales |
Q33814019 | Resolving and dating the phylogeny of Cornales--Effects of taxon sampling, data partitions, and fossil calibrations |
Q92606325 | Restriction-site associated DNA markers provide new insights into the evolutionary history of the bark beetle genus Dendroctonus |
Q36315204 | Retention of duplicated long-wavelength opsins in mosquito lineages by positive selection and differential expression |
Q40113076 | Reticulate evolution in Thuja inferred from multiple gene sequences: implications for the study of biogeographical disjunction between eastern Asia and North America |
Q33595599 | Reticulation, data combination, and inferring evolutionary history: an example from Danthonioideae (Poaceae). |
Q91880128 | Return to the Sea, Get Huge, Beat Cancer: An Analysis of Cetacean Genomes Including an Assembly for the Humpback Whale (Megaptera novaeangliae) |
Q28661002 | Rigorous approaches to species delimitation have significant implications for African crocodilian systematics and conservation |
Q21092254 | Robust time estimation reconciles views of the antiquity of placental mammals |
Q29618902 | Rocks and clocks: calibrating the Tree of Life using fossils and molecules |
Q24651414 | Rosid radiation and the rapid rise of angiosperm-dominated forests |
Q28657953 | Sequencing of chloroplast genomes from wheat, barley, rye and their relatives provides a detailed insight into the evolution of the Triticeae tribe |
Q21136250 | Serpentine Soils Do Not Limit Mycorrhizal Fungal Diversity |
Q82378986 | Serpentine soils promote ectomycorrhizal fungal diversity |
Q64359227 | Sexual Dichromatism Drives Diversification within a Major Radiation of African Amphibians |
Q51550129 | Sexual dichromatism in frogs: natural selection, sexual selection and unexpected diversity. |
Q46253937 | Sexual dimorphism, phenotypic integration, and the evolution of head structure in casque-headed lizards. |
Q33474154 | Sexual selection is involved in speciation in a land snail radiation on crete |
Q92484446 | Sexual selection, body mass and molecular evolution interact to predict diversification in birds |
Q94481811 | Shedding light: a phylotranscriptomic perspective illuminates the origin of photosymbiosis in marine bivalves |
Q30720363 | Shifts in climate foster exceptional opportunities for species radiation: the case of South african geraniums |
Q40359282 | Simplifying a wing: diversity and functional consequences of digital joint reduction in bat wings. |
Q43975184 | Simulating and detecting autocorrelation of molecular evolutionary rates among lineages |
Q67213176 | Simultaneous Bayesian inference of phylogeny and molecular coevolution |
Q47325203 | Single-copy nuclear genes recover cretaceous-age divergences in bees. |
Q28661592 | Size and shape in the evolution of ant worker morphology |
Q37863752 | Skyline-plot methods for estimating demographic history from nucleotide sequences |
Q54998842 | So many genes, so little time: A practical approach to divergence-time estimation in the genomic era. |
Q21283919 | Social complexity in bees is not sufficient to explain lack of reversions to solitary living over long time scales |
Q111629663 | Spatial phylogenetics of the North American flora |
Q46273983 | Spatial phylogenetics of the native California flora. |
Q34070786 | Spatial predictions of phylogenetic diversity in conservation decision making |
Q59125424 | Spatial scale-dependent phylogenetic signal in species distributions along geographic and elevation gradients in a mountainous rangeland |
Q34132310 | Spatially structured populations with a low level of cryptic diversity in European marine Gastrotricha |
Q28960143 | Spatio-Temporal Relationships of the Macaronesian Endemic Flora: A Relictual Series or Window of Opportunity? |
Q33582618 | Spatio-temporal patterns of genome evolution in allotetraploid species of the genus Oryza |
Q35195390 | Speciation and introgression between Mimulus nasutus and Mimulus guttatus |
Q35626313 | Speciation dynamics during the global radiation of extant bats. |
Q56428702 | Speciation inPararge(Satyrinae: Nymphalidae) butterflies - North Africa is the source of ancestral populations of allParargespecies |
Q31030566 | Speciation of Iberian diving beetles in Pleistocene refugia (Coleoptera, Dytiscidae). |
Q46108206 | Speciational evolution of coloration in the genus Carduelis |
Q28743938 | Species delimitation and phylogeography of Aphonopelma hentzi (Araneae, Mygalomorphae, Theraphosidae): cryptic diversity in North American tarantulas |
Q33249970 | Species diversification patterns in the Polynesian jumping spider genus Havaika Prószyński, 2001 (Araneae, Salticidae). |
Q38935385 | Species identification in the taxonomically neglected, highly diverse, neotropical parasitoid wasp genus Notiospathius (Braconidae: Doryctinae) based on an integrative molecular and morphological approach |
Q36008472 | Species introductions and the phylogenetic and functional structure of California's grasses |
Q28603676 | Spider phylogenomics: untangling the Spider Tree of Life |
Q51684508 | Steady Plio-Pleistocene diversification and a 2-million-year sympatry threshold in a New Zealand cicada radiation. |
Q49913452 | Step-wise evolution of complex chemical defenses in millipedes: a phylogenomic approach |
Q42675429 | Strategies for Partitioning Clock Models in Phylogenomic Dating: Application to the Angiosperm Evolutionary Timescale. |
Q51595525 | Strong influence of regional species pools on continent-wide structuring of local communities. |
Q21245337 | Strong mitochondrial DNA support for a Cretaceous origin of modern avian lineages |
Q34570816 | Structure and evolution of the r/b chromosomal regions in rice, maize and sorghum |
Q51704905 | Summarizing a posterior distribution of trees using agreement subtrees. |
Q37153819 | Surviving the K-T mass extinction: new perspectives of polyploidization in angiosperms |
Q28776744 | Synchronous coadaptation in an ancient case of herbivory |
Q34441807 | Synechococcus: 3 billion years of global dominance |
Q28756929 | Synteny and chromosome evolution in the lepidoptera: evidence from mapping in Heliconius melpomene |
Q33513776 | Systematics and biogeography of the Neotropical genus Mabuya, with special emphasis on the Amazonian skink Mabuya nigropunctata (Reptilia, Scincidae). |
Q33234519 | Systematics and historical biogeography of Greater Antillean Cichlidae |
Q104454888 | Systematics and historical biogeography of theAphanius disparspecies group (Teleostei: Aphaniidae) and description of a new species from Southern Iran |
Q21185420 | Systematics of the Neotropical caddisfly genus Notidobiella Schmid (Trichoptera, Sericostomatidae), with the description of 3 new species |
Q39866962 | TIMING DEEP DIVERGENCE EVENTS IN CALCAREOUS DINOFLAGELLATES(1). |
Q28657578 | Tangled up in two: a burst of genome duplications at the end of the Cretaceous and the consequences for plant evolution |
Q92539268 | Target Capture Sequencing Unravels Rubus Evolution |
Q46487357 | Taxon sampling effects in molecular clock dating: an example from the African Restionaceae |
Q46836574 | Tempo of hybrid inviability in centrarchid fishes (Teleostei: Centrarchidae). |
Q28960148 | Temporal and Spatial Diversification of Circum-Mediterranean Compositae-Anthemideae |
Q90888037 | Testing adaptive hypotheses on the evolution of larval life history in acorn and stalked barnacles |
Q35980512 | Testing the Relationships between Diversification, Species Richness, and Trait Evolution |
Q45398526 | Testing the directionality of evolution: the case of chydorid crustaceans |
Q34112527 | Testing the impact of calibration on molecular divergence times using a fossil-rich group: the case of Nothofagus (Fagales). |
Q33246895 | Testing the molecular clock: molecular and paleontological estimates of divergence times in the Echinoidea (Echinodermata). |
Q28261893 | That awkward age for butterflies: insights from the age of the butterfly subfamily Nymphalinae (Lepidoptera: Nymphalidae) |
Q24653779 | The Ediacaran emergence of bilaterians: congruence between the genetic and the geological fossil records |
Q49028136 | The Emergence of Earliest Angiosperms may be Earlier than Fossil Evidence Indicates |
Q28606703 | The First Mitogenome of the Cyprus Mouflon (Ovis gmelini ophion): New Insights into the Phylogeny of the Genus Ovis |
Q57996328 | The Great American Biotic Interchange revisited |
Q22066011 | The Impact of Fossils and Taxon Sampling on Ancient Molecular Dating Analyses |
Q35579280 | The Use of Bioinformatics for Studying HIV Evolutionary and Epidemiological History in South America |
Q55877791 | The age of major monocot groups inferred from 800+rbcL sequences |
Q33220521 | The age of the angiosperms: a molecular timescale without a clock |
Q28755282 | The assembly of montane biotas: linking Andean tectonics and climatic oscillations to independent regimes of diversification in Pionus parrots |
Q56040935 | The beetle tree of life reveals that Coleoptera survived end-Permian mass extinction to diversify during the Cretaceous terrestrial revolution |
Q38912843 | The biogeography and age of salticid spider radiations (Araneae: Salticidae). |
Q21093249 | The colonization of land by animals: molecular phylogeny and divergence times among arthropods |
Q22065328 | The complete plastid genome sequence of Welwitschia mirabilis: an unusually compact plastome with accelerated divergence rates |
Q42630006 | The complex evolutionary history of seeing red: molecular phylogeny and the evolution of an adaptive visual system in deep-sea dragonfishes (Stomiiformes: Stomiidae). |
Q34706250 | The drowning of New Zealand and the problem of Agathis |
Q43027950 | The east-west-north colonization history of the Mediterranean and Europe by the coastal plant Carex extensa (Cyperaceae). |
Q46458544 | The effect of spatial scale on relative influences of assembly processes in temperate stream fish assemblages |
Q35036303 | The evolution of body size, antennal size and host use in parasitoid wasps (Hymenoptera: Chalcidoidea): a phylogenetic comparative analysis |
Q50103968 | The evolution of relative trait size and shape: insights from the genitalia of dung beetles |
Q28749576 | The evolutionary history of the extinct ratite moa and New Zealand Neogene paleogeography |
Q95279994 | The evolutionary origins of the cat attractant nepetalactone in catnip |
Q28742086 | The evolutionary rate dynamically tracks changes in HIV-1 epidemics: application of a simple method for optimizing the evolutionary rate in phylogenetic trees with longitudinal data |
Q47698968 | The first mistletoes: origins of aerial parasitism in Santalales |
Q42438018 | The genus Coleodactylus (Sphaerodactylinae, Gekkota) revisited: a molecular phylogenetic perspective |
Q28767179 | The geological history of deep-sea colonization by echinoids: roles of surface productivity and deep-water ventilation |
Q28742476 | The historical biogeography of Mammalia |
Q42213600 | The impact of calibration and clock-model choice on molecular estimates of divergence times |
Q34119190 | The impact of the representation of fossil calibrations on Bayesian estimation of species divergence times |
Q28587319 | The influence of habitat on the evolution of plants: a case study across Saxifragales |
Q43498385 | The influence of ignoring secondary structure on divergence time estimates from ribosomal RNA genes |
Q28817688 | The interplay between natural and sexual selection in the evolution of sexual size dimorphism in Sceloporus lizards (Squamata: Phrynosomatidae) |
Q41408546 | The lemur revolution starts now: the genomic coming of age for a non-model organism |
Q30422644 | The mercury resistance operon: from an origin in a geothermal environment to an efficient detoxification machine |
Q34348209 | The molecular phylogenetics of endangerment: cryptic variation and historical phylogeography of the California tiger salamander, Ambystoma californiense. |
Q110697130 | The molecular systematics and diversification of a taxonomically unstable group of Asian cicada tribes related to Cicadini Latreille, 1802 (Hemiptera : Cicadidae) |
Q28654917 | The necessity of DNA taxonomy to reveal cryptic diversity and spatial distribution of meiofauna, with a focus on Nemertea |
Q21999008 | The origin and diversification of angiosperms |
Q28767419 | The origin and diversification of eukaryotes: problems with molecular phylogenetics and molecular clock estimation |
Q29618563 | The origin and evolution of model organisms |
Q43529920 | The origin, evolution, and diversification of rockfishes of the genus Sebastes (Cuvier). |
Q28299604 | The pattern and timing of diversification of Philippine endemic rodents: evidence from mitochondrial and nuclear gene sequences |
Q30983794 | The phylogenetic history and biogeography of the frankincense and myrrh family (Burseraceae) based on nuclear and chloroplast sequence data |
Q39148918 | The phylogenetic utility of acetyltransferase (ARD1) and glutaminyl tRNA synthetase (QtRNA) for reconstructing Cenozoic relationships as exemplified by the large Australian cicada Pauropsalta generic complex |
Q51917110 | The phylogeny of the Pentaschistis clade (Danthonioideae, Poaceae) based on chloroplast DNA, and the evolution and loss of complex characters. |
Q21198926 | The phylogeography of Indoplanorbis exustus (Gastropoda: Planorbidae) in Asia |
Q28749639 | The relationships between xylem safety and hydraulic efficiency in the Cupressaceae: the evolution of pit membrane form and function |
Q31147294 | The relative importance of body size and paleoclimatic change as explanatory variables influencing lineage diversification rate: an evolutionary analysis of bullhead catfishes (Siluriformes: Ictaluridae). |
Q28756061 | The relative importance of ecology and geographic isolation for speciation in anoles |
Q47288378 | The role of biotic and abiotic factors in evolution of ant dispersal in the milkwort family (polygalaceae). |
Q41442522 | The role of geography and ecological opportunity in the diversification of day geckos (Phelsuma). |
Q30959578 | The role of morphological data in phylogeny reconstruction |
Q28770095 | The role of phylogenetics in comparative genetics |
Q21283843 | The root of the East African cichlid radiations |
Q21188442 | The taxonomy and diversity of Platerodrilus (Coleoptera, Lycidae) inferred from molecular data and morphology of adults and larvae |
Q33500486 | The timing of neotropical speciation dynamics: a reconstruction of Myiopagis flycatcher diversification using phylogenetic and paleogeographic data |
Q100941111 | The whole-genome sequencing and analysis of a Ganoderma lucidum strain provide insights into the genetic basis of its high triterpene content |
Q55954495 | ThepetDgroup II intron as a species level marker: utility for tree inference and species identification in the diverse genusCampanula (Campanulaceae) |
Q91782338 | Thermal Niche Differentiation in the Benthic Diatom Cylindrotheca closterium (Bacillariophyceae) Complex |
Q58092849 | Thirty clues to the exceptional diversification of flowering plants |
Q34276079 | Three genome-based phylogeny of Cupressaceae s.l.: further evidence for the evolution of gymnosperms and Southern Hemisphere biogeography |
Q29547571 | Time dependency of molecular rate estimates and systematic overestimation of recent divergence times |
Q92840852 | Timing and ecological priority shaped the diversification of sedges in the Himalayas |
Q28768532 | Timing and rate of speciation in Agave (Agavaceae) |
Q39934766 | Timing of morphological and ecological innovations in the cyanobacteria--a key to understanding the rise in atmospheric oxygen |
Q46590240 | Tiny worms from a mighty continent: high diversity and new phylogenetic lineages of African monogeneans |
Q28651064 | To move or to evolve: contrasting patterns of intercontinental connectivity and climatic niche evolution in "Terebinthaceae" (Anacardiaceae and Burseraceae). |
Q47272838 | Toward understanding the distribution of Laurasian frogs: a test of Savage's biogeographical hypothesis using the genus Bombina |
Q28550549 | Towards an integrated phylogenetic classification of the Tremellomycetes |
Q21284096 | Towards resolving Lamiales relationships: insights from rapidly evolving chloroplast sequences |
Q39606807 | Tracing an invasion: landbridges, refugia, and the phylogeography of the Neotropical rattlesnake (Serpentes: Viperidae: Crotalus durissus). |
Q28754318 | Tracing the impact of the Andean uplift on Neotropical plant evolution |
Q28755245 | Triassic origin and early radiation of multicellular volvocine algae |
Q46728916 | Turtle phylogeny: insights from a novel nuclear intron |
Q47272038 | Two chloroplast DNA inversions originated simultaneously during the early evolution of the sunflower family (Asteraceae). |
Q28658966 | Two new fern chloroplasts and decelerated evolution linked to the long generation time in tree ferns |
Q28662094 | Undersampling taxa will underestimate molecular divergence dates: an example from the South american lizard clade liolaemini |
Q42667142 | Understanding the spectacular failure of DNA barcoding in willows (Salix): does this result from a trans-specific selective sweep? |
Q33327201 | Unraveling the evolutionary history of the hyperdiverse ant genus Pheidole (Hymenoptera: Formicidae). |
Q34327659 | Unraveling the evolutionary radiation of the thoracican barnacles using molecular and morphological evidence: a comparison of several divergence time estimation approaches |
Q39437919 | Unraveling the phylogeny of polygrammoid ferns (Polypodiaceae and Grammitidaceae): exploring aspects of the diversification of epiphytic plants |
Q46859060 | Uplift of the Tibetan plateau: evidence from divergence times of glyptosternoid catfishes |
Q30387664 | Use of phylogenetics in the molecular epidemiology and evolutionary studies of viral infections |
Q57657864 | Using DNA taxonomy to investigate the ecological determinants of plankton diversity: explaining the occurrence of Synchaeta spp. (Rotifera, Monogononta) in mountain lakes |
Q33398939 | Using fossils and molecular data to reveal the origins of the Cape proteas (subfamily Proteoideae). |
Q44168741 | Using fossils to break long branches in molecular dating: a comparison of relaxed clocks applied to the origin of angiosperms |
Q30804393 | Using multiple relaxed-clock models to estimate evolutionary timescales from DNA sequence data |
Q30381140 | Using non-homogeneous models of nucleotide substitution to identify host shift events: application to the origin of the 1918 'Spanish' influenza pandemic virus. |
Q28484414 | Using phylogenetic and coalescent methods to understand the species diversity in the Cladia aggregata complex (Ascomycota, Lecanorales) |
Q22066318 | Using plastid genome-scale data to resolve enigmatic relationships among basal angiosperms |
Q89818403 | Utility of targeted sequence capture for phylogenomics in rapid, recent angiosperm radiations: Neotropical Burmeistera bellflowers as a case study |
Q44036979 | Utility of the nuclear protein-coding gene, elongation factor-1 gamma (EF-1gamma), for spider systematics, emphasizing family level relationships of tarantulas and their kin (Araneae: Mygalomorphae). |
Q28748574 | Variation in DNA substitution rates among lineages erroneously inferred from simulated clock-like data |
Q28748445 | Vertical transmission as the key to the colonization of Madagascar by fungus-growing termites? |
Q54759464 | Vicariance or long-distance dispersal: historical biogeography of the pantropical subfamily Chrysophylloideae (Sapotaceae) |
Q30370595 | Viral diversity and clonal evolution from unphased genomic data. |
Q37775232 | Watching the clock: studying variation in rates of molecular evolution between species |
Q30573919 | Waterscape genetics of the yellow perch (Perca flavescens): patterns across large connected ecosystems and isolated relict populations |
Q36108793 | What explains patterns of species richness? The relative importance of climatic-niche evolution, morphological evolution, and ecological limits in salamanders |
Q40676454 | Which came first: The lizard or the egg? Robustness in phylogenetic reconstruction of ancestral states |
Q36517053 | White-nose syndrome without borders: Pseudogymnoascus destructans infection tolerated in Europe and Palearctic Asia but not in North America |
Q42717087 | White-tailed deer are a biotic filter during community assembly, reducing species and phylogenetic diversity |
Q35958556 | Whole-Genome Identification, Phylogeny, and Evolution of the Cytochrome P450 Family 2 (CYP2) Subfamilies in Birds |
Q22066015 | Whole-mtDNA Genome Sequence Analysis of Ancient African Lineages |
Q37163441 | Widespread adaptive evolution during repeated evolutionary radiations in New World lupins |
Q28714394 | Widespread and persistent invasions of terrestrial habitats coincident with larval feeding behavior transitions during snail-killing fly evolution (Diptera: Sciomyzidae) |
Q40680392 | Widespread flower color convergence in Solanaceae via alternate biochemical pathways |
Q28651633 | Willis, K.J., McElwain, J.C. The evolution of plants |
Q51628874 | [FeFe]-hydrogenase in Yellowstone National Park: evidence for dispersal limitation and phylogenetic niche conservatism. |
Q45078874 | treePL: divergence time estimation using penalized likelihood for large phylogenies |
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