| scholarly article | Q13442814 |
| P50 | author | Amy Reed McCune | Q25441499 |
| Daniel L. Rabosky | Q28735317 | ||
| P2860 | cites work | On the Origin of Species | Q20968204 |
| Ecological limits and diversification rate: alternative paradigms to explain the variation in species richness among clades and regions | Q22065670 | ||
| Darwin's abominable mystery: Insights from a supertree of the angiosperms | Q24621983 | ||
| Evolution of a climbing habit promotes diversification in flowering plants | Q24677947 | ||
| Pollinator shifts drive increasingly long nectar spurs in columbine flowers | Q28305322 | ||
| Exceptional among-lineage variation in diversification rates during the radiation of Australia's most diverse vertebrate clade | Q28755143 | ||
| Increasing morphological complexity in multiple parallel lineages of the Crustacea | Q28755155 | ||
| A Bayesian approach for evaluating the impact of historical events on rates of diversification | Q28755333 | ||
| Clade-specific morphological diversification and adaptive radiation in Hawaiian songbirds | Q28765788 | ||
| A theory of evolution above the species level | Q28775745 | ||
| Species selection on variability | Q28775904 | ||
| Absolute diversification rates in angiosperm clades | Q29547826 | ||
| A comprehensive phylogeny of beetles reveals the evolutionary origins of a superradiation | Q29616341 | ||
| Estimating diversification rates from phylogenetic information | Q29617263 | ||
| The reconstructed evolutionary process | Q29618246 | ||
| Explosive evolutionary radiations: decreasing speciation or increasing extinction through time? | Q29618900 | ||
| Estimating a binary character's effect on speciation and extinction | Q29618906 | ||
| The role of diversification in causing the correlates of dioecy | Q31063903 | ||
| Nonstochastic variation of species-level diversification rates within angiosperms | Q31139339 | ||
| Correlates of species richness in mammals: body size, life history, and ecology | Q31156969 | ||
| Environment, area, and diversification in the species-rich flowering plant family Iridaceae | Q33225154 | ||
| Confounding asymmetries in evolutionary diversification and character change | Q33259182 | ||
| Global variation in the diversification rate of passerine birds | Q33262885 | ||
| Evolutionary diversification of clades of squamate reptiles | Q33294919 | ||
| Engines of speciation: a comparative study in birds of prey | Q33321023 | ||
| Molecular phylogenies link rates of evolution and speciation | Q34535773 | ||
| Linking floral symmetry genes to breeding system evolution | Q36650005 | ||
| Sexual conflict promotes speciation in insects | Q37247503 | ||
| Biotic interactions and macroevolution: extensions and mismatches across scales and levels | Q43875486 | ||
| Larval ecology, geographic range, and species survivorship in Cretaceous mollusks: organismic versus species-level explanations | Q47184684 | ||
| Species richness in agamid lizards: chance, body size, sexual selection or ecology? | Q47436466 | ||
| Sexual conflict does not drive reproductive isolation in experimental populations of Drosophila pseudoobscura | Q48387578 | ||
| No evidence that experimental manipulation of sexual conflict drives premating reproductive isolation in Drosophila melanogaster | Q48443420 | ||
| Ecology predicts large-scale patterns of phylogenetic diversification in birds. | Q50786137 | ||
| Ecological limits on clade diversification in higher taxa. | Q51180685 | ||
| Is evolvability evolvable? | Q51697895 | ||
| Darwinism and the expansion of evolutionary theory. | Q52413792 | ||
| Micro- and macroevolution: scale and hierarchy in evolutionary biology and paleobiology | Q54084439 | ||
| Floral symmetry affects speciation rates in angiosperms. | Q55208690 | ||
| Can adaptation lead to extinction? | Q56067250 | ||
| Behavioural flexibility predicts species richness in birds, but not extinction risk | Q56942254 | ||
| Nonrandom extinction leads to elevated loss of angiosperm evolutionary history | Q56945014 | ||
| Macroecology and extinction risk correlates of frogs | Q57006774 | ||
| Macroevolution of hoverflies (Diptera: Syrphidae): the effect of using higher-level taxa in studies of biodiversity, and correlates of species richness | Q57007001 | ||
| EVOLUTIONARY RATES AND SPECIES DIVERSITY IN FLOWERING PLANTS | Q57069444 | ||
| Relating Traits to Diversification: A Simple Test | Q57193675 | ||
| Sexually Selected Traits Predict Patterns of Species Richness in a Diverse Clade of Suboscine Birds | Q57267717 | ||
| Sexual selection and taxonomic diversity in passerine birds | Q60390628 | ||
| The Role of Local Species Abundance in the Evolution of Pollinator Attraction in Flowering Plants | Q63379841 | ||
| When looks can kill: the evolution of sexually dimorphic floral display and the extinction of dioecious plants | Q63379845 | ||
| Mating preferences, sexual selection and patterns of cladogenesis in ray-finned fishes | Q79787809 | ||
| Heritability at the species level: analysis of geographic ranges of cretaceous mollusks | Q81200916 | ||
| Is cladogenesis heritable? | Q94171095 | ||
| EXTINCTION VULNERABILITY AND SELECTIVITY:Combining Ecological and Paleontological Views | Q104206016 | ||
| P433 | issue | 2 | |
| P921 | main subject | phylogenetics | Q171184 |
| P1104 | number of pages | 7 | |
| P304 | page(s) | 68-74 | |
| P577 | publication date | 2009-09-07 | |
| P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
| P1476 | title | Reinventing species selection with molecular phylogenies. | |
| P478 | volume | 25 |
| Q34351365 | An integrative view of phylogenetic comparative methods: connections to population genetics, community ecology, and paleobiology |
| Q45189078 | Are range-size distributions consistent with species-level heritability? |
| Q55922543 | Bayesian estimation of fossil phylogenies and the evolution of early to middle Paleozoic crinoids (Echinodermata) |
| Q38689758 | Body size evolution in an old insect order: No evidence for Cope's Rule in spite of fitness benefits of large size |
| Q47287758 | Chromosome number evolves independently of genome size in a clade with nonlocalized centromeres (Carex: Cyperaceae). |
| Q28658926 | Clade age and diversification rate variation explain disparity in species richness among water scavenger beetle (Hydrophilidae) lineages |
| Q28728090 | Clade age and species richness are decoupled across the eukaryotic tree of life |
| Q58033692 | Comment on “Does constructive neutral evolution play an important role in the origin of cellular complexity?” DOI 10.1002/bies.201100010 |
| Q28661481 | Corolla morphology influences diversification rates in bifid toadflaxes (Linaria sect. Versicolores) |
| Q35802656 | Detecting Macroevolutionary Self-Destruction from Phylogenies |
| Q40771400 | Evidence of Statistical Inconsistency of Phylogenetic Methods in the Presence of Multiple Sequence Alignment Uncertainty |
| Q33722639 | Evidence of extreme habitat stability in a Southeast Asian biodiversity hotspot based on the evolutionary analysis of neotenic net‐winged beetles |
| Q38953331 | Evolution in a Community Context: On Integrating Ecological Interactions and Macroevolution. |
| Q38738829 | Evolutionary bottlenecks in brackish water habitats drive the colonization of fresh water by stingrays. |
| Q30859028 | Evolutionary bursts in Euphorbia (Euphorbiaceae) are linked with photosynthetic pathway. |
| Q46916402 | Evolutionary relationships among scyphozoan jellyfish families based on complete taxon sampling and phylogenetic analyses of 18S and 28S ribosomal DNA. |
| Q35945499 | Extinction as a driver of avian latitudinal diversity gradients |
| Q34119273 | Extinction, ecological opportunity, and the origins of global snake diversity |
| Q28659080 | Floral specialization and angiosperm diversity: phenotypic divergence, fitness trade-offs and realized pollination accuracy |
| Q21090883 | Four new bat species (Rhinolophus hildebrandtii complex) reflect Plio-Pleistocene divergence of dwarfs and giants across an Afromontane archipelago |
| Q57067330 | High extinction rates and non-adaptive radiation explains patterns of low diversity and extreme morphological disparity in North American blister beetles (Coleoptera, Meloidae) |
| Q28742479 | How diversification rates and diversity limits combine to create large-scale species-area relationships |
| Q38234467 | How traits shape trees: new approaches for detecting character state-dependent lineage diversification |
| Q57006653 | Inclusion of a near-complete fossil record reveals speciation-related molecular evolution |
| Q38082810 | Is self-fertilization an evolutionary dead end? |
| Q38131626 | Is there room for punctuated equilibrium in macroevolution? |
| Q28658273 | Long-term morphological stasis maintained by a plant-pollinator mutualism |
| Q37191964 | Macroevolutionary speciation rates are decoupled from the evolution of intrinsic reproductive isolation in Drosophila and birds |
| Q35545040 | Model inadequacy and mistaken inferences of trait-dependent speciation |
| Q28608099 | Multilevel Selection Theory and the Evolutionary Functions of Transposable Elements |
| Q28602428 | Non-equilibrium dynamics and floral trait interactions shape extant angiosperm diversity |
| Q28600839 | Omnivory in birds is a macroevolutionary sink |
| Q38152130 | Phylogenetic estimates of speciation and extinction rates for testing ecological and evolutionary hypotheses |
| Q34249770 | Population-level consequences of polymorphism, plasticity and randomized phenotype switching: a review of predictions. |
| Q34352634 | Positive correlation between diversification rates and phenotypic evolvability can mimic punctuated equilibrium on molecular phylogenies |
| Q33711748 | Primary Controls on Species Richness in Higher Taxa |
| Q85116592 | Quantitative Traits and Diversification |
| Q28602551 | Species Selection Favors Dispersive Life Histories in Sea Slugs, but Higher Per-Offspring Investment Drives Shifts to Short-Lived Larvae |
| Q46595357 | Species selection and random drift in macroevolution |
| Q34752954 | Species selection and the macroevolution of coral coloniality and photosymbiosis |
| Q55279495 | The Role of Transposable Elements in Speciation. |
| Q35544409 | The evolutionary reality of species and higher taxa in plants: a survey of post-modern opinion and evidence |
| Q28637735 | The extended Price equation quantifies species selection on mammalian body size across the Palaeocene/Eocene Thermal Maximum |
| Q34120887 | Trait-dependent diversification and the impact of palaeontological data on evolutionary hypothesis testing in New World ratsnakes (tribe Lampropeltini). |
| Q28535569 | Understanding phenotypical character evolution in parmelioid lichenized fungi (Parmeliaceae, Ascomycota) |
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