Is BAMM flawed? Theoretical and practical concerns in the analysis of multi-rate diversification models.
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Environmentally driven extinction and opportunistic origination explain fern diversification patternsBiological factors contributing to bark and ambrosia beetle species diversification.A major shift in diversification rate helps explain macroevolutionary patterns in primate species diversity.Evolutionary radiations in the species-rich mountain genus Saxifraga L.Positive association between population genetic differentiation and speciation rates in New World birds.Hostplant change and paleoclimatic events explain diversification shifts in skipper butterflies (Family: Hesperiidae)Insights into the historical assembly of East Asian subtropical evergreen broadleaved forests revealed by the temporal history of the tea family.Evolutionary bottlenecks in brackish water habitats drive the colonization of fresh water by stingrays.Lineage diversity and size disparity in Musteloidea: testing patterns of adaptive radiation using molecular and fossil-based methods.Ecological opportunity alters the timing and shape of adaptive radiation.Seed size and its rate of evolution correlate with species diversification across angiosperms.Total evidence phylogeny and evolutionary timescale for Australian faunivorous marsupials (Dasyuromorphia).Estimating diversification rates for higher taxa: BAMM can give problematic estimates of rates and rate shifts.Both temperature fluctuations and East Asian monsoons have driven plant diversification in the karst ecosystems from southern China.Speciation below ground: Tempo and mode of diversification in a radiation of endogean ground beetles.The evolution of floral sonication, a pollen foraging behavior used by bees (Anthophila).Shifts in diversification rates and host jump frequencies shaped the diversity of host range among Sclerotiniaceae fungal plant pathogens.Dry habitats were crucibles of domestication in the evolution of agriculture in ants.Island- and lake-like parallel adaptive radiations replicated in rivers.Ecological opportunity may facilitate diversification in Palearctic freshwater organisms: a case study on hydrobiid gastropods.Testing the impact of effective population size on speciation rates - a negative correlation or lack thereof in lichenized fungi.Macroecology and macroevolution of the latitudinal diversity gradient in ants.Comparing the rates of speciation and extinction between phylogenetic trees.Multiple and Independent Phases of Transposable Element Amplification in the Genomes of Piciformes (Woodpeckers and Allies).A phylogeny of kingfishers reveals an Indomalayan origin and elevated rates of diversification on oceanic islandsSpatio-temporal evolution of L. in the Qinghai-Tibet-Plateau region: Immigration and radiationWhat affects power to estimate speciation rate shifts?Multilocus molecular systematics of the circumtropical reef-fish genus (Pomacentridae): history, geography and ecology of speciationClimate and host-plant associations shaped the evolution of ceutorhynch weevils throughout the Cenozoic
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Is BAMM flawed? Theoretical and practical concerns in the analysis of multi-rate diversification models.
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Is BAMM flawed? Theoretical an ...... i-rate diversification models.
@ast
Is BAMM flawed? Theoretical an ...... i-rate diversification models.
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type
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Is BAMM flawed? Theoretical an ...... i-rate diversification models.
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Is BAMM flawed? Theoretical an ...... i-rate diversification models.
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Is BAMM flawed? Theoretical an ...... i-rate diversification models.
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Is BAMM flawed? Theoretical an ...... i-rate diversification models.
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P2860
P356
P1433
P1476
Is BAMM flawed? Theoretical an ...... i-rate diversification models.
@en
P2093
Daniel L Rabosky
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P304
P356
10.1093/SYSBIO/SYX037
P577
2017-02-21T00:00:00Z