scholarly article | Q13442814 |
P5530 | Altmetric DOI | 10.1016/J.TREE.2015.11.005 |
P6409 | CORE ID | 41991787 |
P6179 | Dimensions Publication ID | 1006957209 |
P356 | DOI | 10.1016/J.TREE.2015.11.005 |
P953 | full work available at URL | http://eprints.whiterose.ac.uk/103035/ |
P698 | PubMed publication ID | 26701706 |
P1154 | Scopus EID | 2-s2.0-84955717279 |
P50 | author | William E. Kunin | Q47354225 |
Jacob B Socolar | Q56420837 | ||
P2093 | author name string | David P Edwards | |
James J Gilroy | |||
P2860 | cites work | Species Invasions Exceed Extinctions on Islands Worldwide: A Comparative Study of Plants and Birds | Q22066123 |
Has the Earth’s sixth mass extinction already arrived? | Q24289328 | ||
Accelerating extinction risk from climate change | Q24577138 | ||
Avian extinction and mammalian introductions on oceanic islands | Q28284706 | ||
The interaction between predation and competition | Q28300690 | ||
Magnitude and variation of prehistoric bird extinctions in the Pacific | Q28708885 | ||
Measuring β-diversity with species abundance data | Q28830774 | ||
Measuring beta diversity for presence-absence data | Q29010510 | ||
The biodiversity of species and their rates of extinction, distribution, and protection | Q30049273 | ||
Zeta Diversity as a Concept and Metric That Unifies Incidence-Based Biodiversity Patterns | Q30052494 | ||
A diversity of beta diversities: straightening up a concept gone awry. Part 1. Defining beta diversity as a function of alpha and gamma diversity | Q30054430 | ||
A social and ecological assessment of tropical land uses at multiple scales: the Sustainable Amazon Network | Q30391576 | ||
Putting beta-diversity on the map: broad-scale congruence and coincidence in the extremes | Q30444302 | ||
Combining high biodiversity with high yields in tropical agroforests. | Q30500427 | ||
Cryptic loss of montane avian richness and high community turnover over 100 years. | Q30628673 | ||
Assemblage time series reveal biodiversity change but not systematic loss | Q30803680 | ||
Directionality of recent bird distribution shifts and climate change in Great Britain. | Q30875299 | ||
Fifteen forms of biodiversity trend in the Anthropocene | Q30881968 | ||
Climate change and the migration capacity of species | Q31040707 | ||
Higher levels of multiple ecosystem services are found in forests with more tree species | Q31110758 | ||
Additive partitioning of rarefaction curves and species-area relationships: unifying alpha-, beta- and gamma-diversity with sample size and habitat area | Q33254223 | ||
Beta diversity at different spatial scales: plant communities in organic and conventional agriculture | Q33261803 | ||
Species-area relationships from a spatially explicit neutral model in an infinite landscape | Q33286426 | ||
Prehistoric extinctions of pacific island birds: biodiversity meets zooarchaeology | Q33297098 | ||
Tree recruitment in an empty forest | Q33347715 | ||
Linking global turnover of species and environments | Q33383724 | ||
Beta diversity along environmental gradients: implications of habitat specialization in tropical montane landscapes | Q33387938 | ||
Birds track their Grinnellian niche through a century of climate change | Q33508734 | ||
Alpha and beta diversity of plants and animals along a tropical land-use gradient | Q33518827 | ||
Navigating the multiple meanings of β diversity: a roadmap for the practicing ecologist. | Q33744367 | ||
Targeting global protected area expansion for imperiled biodiversity. | Q33799935 | ||
Ecological impacts of invasive alien plants: a meta-analysis of their effects on species, communities and ecosystems | Q33904581 | ||
Reconciling food production and biodiversity conservation: land sharing and land sparing compared | Q34008306 | ||
Disentangling the drivers of β diversity along latitudinal and elevational gradients. | Q34028313 | ||
Enemies maintain hyperdiverse tropical forests | Q34155639 | ||
Intensive agriculture erodes β-diversity at large scales | Q34315283 | ||
Conversion of the Amazon rainforest to agriculture results in biotic homogenization of soil bacterial communities | Q34524450 | ||
Invasive plants have scale-dependent effects on diversity by altering species-area relationships | Q34553298 | ||
Land-sharing versus land-sparing logging: reconciling timber extraction with biodiversity conservation. | Q34954505 | ||
Impact of logging and forest conversion to oil palm plantations on soil bacterial communities in Borneo | Q34993773 | ||
Global meta-analysis reveals no net change in local-scale plant biodiversity over time | Q35027576 | ||
Agricultural expansion and its impacts on tropical nature | Q35081708 | ||
Defaunation in the Anthropocene | Q35212976 | ||
Loss of avian phylogenetic diversity in neotropical agricultural systems | Q35249509 | ||
Biotic homogenization and differentiation of soil faunal communities in the production forest landscape: taxonomic and functional perspectives. | Q35342141 | ||
Non-native plants add to the British flora without negative consequences for native diversity | Q35378187 | ||
Null model approaches to evaluating the relative role of different assembly processes in shaping ecological communities | Q35486959 | ||
Mitigating the impact of oil-palm monoculture on freshwater fishes in Southeast Asia | Q35584630 | ||
How pervasive is biotic homogenization in human-modified tropical forest landscapes? | Q35753178 | ||
The Anthropocene concept in ecology and conservation | Q38281915 | ||
No universal scale-dependent impacts of invasive species on native plant species richness | Q39491980 | ||
Dispersal, environment, and floristic variation of western Amazonian forests. | Q39537955 | ||
A comparison of land-sharing and land-sparing strategies for plant richness conservation in agricultural landscapes | Q42649140 | ||
Biotic homogenization: a few winners replacing many losers in the next mass extinction | Q45241136 | ||
Effects of habitat fragmentation and isolation on species richness: evidence from biogeographic patterns | Q46240871 | ||
Dispersal, environmental niches and oceanic-scale turnover in deep-sea bivalves. | Q51467151 | ||
A global analysis of the impacts of urbanization on bird and plant diversity reveals key anthropogenic drivers. | Q51469503 | ||
Degraded lands worth protecting: the biological importance of Southeast Asia's repeatedly logged forests. | Q52707964 | ||
Beta diversity of urban floras among European and non-European cities | Q56450711 | ||
Gains in native species promote biotic homogenization over four decades in a human-dominated landscape | Q56474032 | ||
Biotic homogenization at the community scale: disentangling the roles of urbanization and plant invasion | Q56490239 | ||
Phylogenetic beta diversity of native and alien species in European urban floras | Q56557449 | ||
Urbanization as a major cause of biotic homogenization | Q56781794 | ||
Urbanization and homogenization – Comparing the floras of urban and rural areas in Germany | Q56781807 | ||
Homogenization of ant communities in mediterranean California: The effects of urbanization and invasion | Q56781810 | ||
Stochastic and deterministic drivers of spatial and temporal turnover in breeding bird communities | Q56936822 | ||
Spatial scale of observation affects alpha, beta and gamma diversity of cavity-nesting bees and wasps across a tropical land-use gradient | Q56937156 | ||
Alpha and beta diversity of arthropods and plants in organically and conventionally managed wheat fields | Q57002083 | ||
Homogenization of forest plant communities and weakening of species?environment relationships via agricultural land use | Q57006146 | ||
Effects of landscape structure and land-use intensity on similarity of plant and animal communities | Q57010941 | ||
Partitioning diversity for conservation analyses | Q57035677 | ||
Contrasting effects of natural and anthropogenic stressors on beta diversity in river organisms | Q57057101 | ||
The impact of urbanization on taxonomic and functional similarity among bird communities | Q57197001 | ||
Multiple site dissimilarity quantifies compositional heterogeneity among several sites, while average pairwise dissimilarity may be misleading | Q57205101 | ||
Partitioning the turnover and nestedness components of beta diversity | Q57205111 | ||
Ecological filtering or random extinction? Beta-diversity patterns and the importance of niche-based and neutral processes following habitat loss | Q57212193 | ||
Are cities different? Patterns of species richness and beta diversity of urban bird communities and regional species assemblages in Europe | Q57236240 | ||
Island Biogeography Theory and Conservation Practice | Q57481787 | ||
Rarefaction and extrapolation with Hill numbers: a framework for sampling and estimation in species diversity studies | Q58042407 | ||
Towards a unified descriptive theory for spatial ecology: predicting biodiversity patterns across spatial scales | Q58421747 | ||
Contrasting patterns of turnover between plants, pollinators and their interactions | Q59270427 | ||
Using null models to disentangle variation in community dissimilarity from variation in α-diversity | Q60146416 | ||
Focus on poleward shifts in species' distribution underestimates the fingerprint of climate change | Q60334473 | ||
Spatial modelling of species turnover identifies climate ecotones, climate change tipping points and vulnerable taxonomic groups | Q60346975 | ||
Avian species composition across the Amazon River: the roles of dispersal limitation and environmental heterogeneity | Q60463911 | ||
Spatial scale of similarity as an indicator of metacommunity stability in exploited marine systems | Q61193238 | ||
Are there latitudinal gradients in species turnover? | Q104206773 | ||
P433 | issue | 1 | |
P921 | main subject | beta diversity | Q36039 |
biodiversity | Q47041 | ||
biodiversity conservation | Q126019871 | ||
P1104 | number of pages | 14 | |
P304 | page(s) | 67-80 | |
P577 | publication date | 2015-12-14 | |
P1433 | published in | Trends in Ecology & Evolution | Q15265725 |
P1476 | title | How Should Beta-Diversity Inform Biodiversity Conservation? | |
P478 | volume | 31 |
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Q58656622 | A meta-analysis of nestedness and turnover components of beta diversity across organisms and ecosystems |
Q38611847 | Agriculture erases climate-driven β-diversity in Neotropical bird communities. |
Q110697773 | Alpha and beta diversity of planktonic microcrustaceans are associated with environmental heterogeneity in the Frades River Basin, Brazil |
Q116673922 | Avifaunal diversity in Indian Institute of Technology Guwahati Campus, Assam, India |
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Q57068384 | Biodiversity change is uncoupled from species richness trends: Consequences for conservation and monitoring |
Q46252060 | Biodiversity conservation values of fragmented communally reserved forests, managed by indigenous people, in a human-modified landscape in Borneo |
Q92747206 | Biotic homogenization within and across eight widely distributed grasslands following invasion by Bromus inermis |
Q100416634 | Cannot see the diversity for all the species: Evaluating inclusion criteria for local species lists when using abundant citizen science data |
Q90245876 | Chronic disturbance modulates symbiont (Symbiodiniaceae) beta diversity on a coral reef |
Q56837339 | Community heterogeneity of aquatic macroinvertebrates in urban ponds at a multi-city scale |
Q92216141 | Congruence between arthropod and plant diversity in a biodiversity hotspot largely driven by underlying abiotic factors |
Q46525205 | Conservation: The rainforest's 'do not disturb' signs |
Q90840016 | Contrasting effects of plant diversity on β- and γ-diversity of grassland invertebrates |
Q92431842 | Coordinated community structure among trees, fungi and invertebrate groups in Amazonian rainforests |
Q55284308 | Cross-shelf investigation of coral reef cryptic benthic organisms reveals diversity patterns of the hidden majority. |
Q46575326 | Current Uses of Beta-Diversity in Biodiversity Conservation: A response to Socolar et al. |
Q48105179 | Different in the dark: The effect of habitat characteristics on community composition and beta diversity in bromeliad microfauna. |
Q28597013 | Disentangling the drivers of taxonomic and phylogenetic beta diversities in disturbed and undisturbed subtropical forests |
Q46431842 | Dispersal and neutral sampling mediate contingent effects of disturbance on plant beta-diversity: a meta-analysis. |
Q56961359 | Dissecting global turnover in vascular plants |
Q50026473 | Divergent biodiversity change within ecosystems |
Q58482834 | Diversity patterns of alien and native plant species in Trieste port area: exploring the role of urban habitats in biodiversity conservation |
Q90428153 | Ecological networks reveal contrasting patterns of bacterial and fungal communities in glacier-fed streams in Central Asia |
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Q57176130 | Expected impacts of climate change threaten the anuran diversity in the Brazilian hotspots |
Q46268320 | Freshwater eutrophication drives sharp reductions in temporal beta diversity. |
Q55124185 | Habitat quality is more important than matrix quality for bird communities in protected areas. |
Q113714417 | Impacts of a novel controlled-release TiO2-coated (nano-) formulation of carbendazim and its constituents on freshwater macroinvertebrate communities |
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Q101217343 | Lake productivity and waterbird functional diversity across geographic and environmental gradients in temperate China |
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Q90003018 | Local species diversity, β-diversity and climate influence the regional stability of bird biomass across North America |
Q58724684 | Local-scale determinants of arboreal spider beta diversity in a temperate forest: roles of tree architecture, spatial distance, and dispersal capacity |
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Q92022083 | Measuring continuous compositional change using decline and decay in zeta diversity |
Q60547174 | Methods for phylogenetic analysis of microbiome data |
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Q92770020 | Nestedness of waterbird assemblages in the subsidence wetlands recently created by underground coal mining |
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Q55091752 | Population Abundance and Ecosystem Service Provision: The Case of Birds. |
Q46270173 | Predicting temporal variation in zooplankton beta diversity is challenging |
Q51144232 | Questioning the Alienation of Native Species from Invasion Ecology: A Reply to Tong et al. |
Q55053122 | Reconciling biodiversity and carbon stock conservation in an Afrotropical forest landscape. |
Q51148897 | Reliable estimates of beta diversity with incomplete sampling. |
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Q46104130 | Scale-specific drivers of kelp forest communities. |
Q90412985 | Small mammal species richness and turnover along elevational gradient in Yulong Mountain, Yunnan, Southwest China |
Q44008136 | Sparse Data Necessitate Explicit Treatment of Beta-Diversity: A Reply to Bush et al. |
Q91656957 | Spatial eco-evolutionary feedbacks mediate coexistence in prey-predator systems |
Q46273325 | Spatial-temporal dynamics of neotropical velvet ant (Hymenoptera: Mutillidae) communities along a forest-savanna gradient |
Q97905339 | Species richness and beta diversity patterns of multiple taxa along an elevational gradient in pastured grasslands in the European Alps |
Q60300387 | Species turnover in plants does not predict turnover in flower-visiting insects |
Q92155009 | Species-specific responses to habitat conversion across scales synergistically restructure Neotropical bird communities |
Q46309456 | The Nebulous Ecology of Native Invasions. |
Q57027561 | The effect of fire history in shaping diversity patterns of flower-visiting insects in post-fire Mediterranean pine forests |
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Q52565474 | Uniqueness of Protected Areas for Conservation Strategies in the European Union. |
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