Pages that link to "Q28756973"
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The following pages link to Colloquium paper: extinction and the spatial dynamics of biodiversity (Q28756973):
Displaying 50 items.
- Colloquium paper: in the light of evolution II: biodiversity and extinction (Q22066294) (← links)
- Has the Earth’s sixth mass extinction already arrived? (Q24289328) (← links)
- Mass extinction of lizards and snakes at the Cretaceous-Paleogene boundary (Q24634106) (← links)
- Ecomorphological selectivity among marine teleost fishes during the end-Cretaceous extinction (Q24649103) (← links)
- Direct and indirect effects of biological factors on extinction risk in fossil bivalves (Q28133152) (← links)
- Greenhouse-icehouse transition in the Late Ordovician marks a step change in extinction regime in the marine plankton (Q28604006) (← links)
- Extinction risk of soil biota (Q28606572) (← links)
- An analysis of pterosaurian biogeography: implications for the evolutionary history and fossil record quality of the first flying vertebrates (Q28611063) (← links)
- Severity of ocean acidification following the end-Cretaceous asteroid impact (Q28646365) (← links)
- The Early Origin of the Antarctic Marine Fauna and Its Evolutionary Implications (Q28649995) (← links)
- Out of the tropics, but how? Fossils, bridge species, and thermal ranges in the dynamics of the marine latitudinal diversity gradient (Q28680783) (← links)
- Bivalve network reveals latitudinal selectivity gradient at the end-Cretaceous mass extinction (Q28705211) (← links)
- Disturbances, organisms and ecosystems: a global change perspective (Q28708889) (← links)
- Long-term differences in extinction risk among the seven forms of rarity (Q28713158) (← links)
- Biodiversity tracks temperature over time (Q28727461) (← links)
- Graptoloid diversity and disparity became decoupled during the Ordovician mass extinction (Q28731493) (← links)
- Multi-variate models are essential for understanding vertebrate diversification in deep time (Q28732794) (← links)
- Detecting shifts in diversity limits from molecular phylogenies: what can we know? (Q28740622) (← links)
- Leaf evolution in Southern Hemisphere conifers tracks the angiosperm ecological radiation (Q28742282) (← links)
- How diversification rates and diversity limits combine to create large-scale species-area relationships (Q28742479) (← links)
- Environmental change drove macroevolution in cupuladriid bryozoans (Q28749014) (← links)
- Repeated loss of coloniality and symbiosis in scleractinian corals (Q28750437) (← links)
- Reply to Smith and O'Meara: The utility of morphogenera (Q28751665) (← links)
- (Q28763716) (redirect page) (← links)
- Potential pitfalls of reconstructing deep time evolutionary history with only extant data, a case study using the canidae (mammalia, carnivora). (Q30672936) (← links)
- Neotropical biodiversity: timing and potential drivers (Q33942692) (← links)
- Paleoecoinformatics: applying geohistorical data to ecological questions (Q34048613) (← links)
- The latitudinal biodiversity gradient through deep time (Q35020691) (← links)
- Mutualistic mimicry enhances species diversification through spatial segregation and extension of the ecological niche space. (Q36262251) (← links)
- Geographic range did not confer resilience to extinction in terrestrial vertebrates at the end-Triassic crisis (Q39280373) (← links)
- Severe extinction and rapid recovery of mammals across the Cretaceous-Palaeogene boundary, and the effects of rarity on patterns of extinction and recovery. (Q39775323) (← links)
- Phylogenetic conservatism of extinctions in marine bivalves (Q39957288) (← links)
- Taxonomy and Phylogeny Can Yield Comparable Results in Comparative Paleontological Analyses (Q41169033) (← links)
- Origins, bottlenecks, and present-day diversity: patterns of morphospace occupation in marine bivalves (Q41543698) (← links)
- Approaches to Macroevolution: 2. Sorting of Variation, Some Overarching Issues, and General Conclusions (Q45717976) (← links)
- Evolution of paedomorphosis in plethodontid salamanders: ecological correlates and re-evolution of metamorphosis (Q46985986) (← links)
- Contrasting responses of functional diversity to major losses in taxonomic diversity (Q47176860) (← links)
- The old and the new plankton: ecological replacement of associations of mollusc plankton and giant filter feeders after the Cretaceous? (Q49333433) (← links)
- Mammal body size evolution in North America and Europe over 20 Myr: similar trends generated by different processes. (Q51229179) (← links)
- Correlations of Life-History and Distributional-Range Variation with Salamander Diversification Rates: Evidence for Species Selection (Q51874383) (← links)
- River networks as ecological corridors: A coherent ecohydrological perspective. (Q53830522) (← links)
- The Anthropocene biosphere (Q55868918) (← links)
- Greenhouse biogeography: the relationship of geographic range to invasion and extinction in the Cretaceous Western Interior Seaway (Q56462010) (← links)
- The biogeographical imprint of mass extinctions (Q56520793) (← links)
- Rise and fall in diversity of Neogene marine vertebrates on the temperate Pacific coast of South America (Q56551539) (← links)
- New and Mesozoic-relict mollusks from Paleocene wood-fall communities in Urahoro Town, eastern Hokkaido, northern Japan (Q56553277) (← links)
- Latitudinal shifts of introduced species: possible causes and implications (Q56570679) (← links)
- Species living in harsh environments have low clade rank and are localized on former Laurasian continents: a case study ofWillemia(Collembola) (Q56814587) (← links)
- Evolutionary rates of mid-Permian tetrapods from South Africa and the role of temporal resolution in turnover reconstruction (Q57258454) (← links)
- Phylogenetic signal in extinction selectivity in Devonian terebratulide brachiopods (Q57399706) (← links)