Abstract is: Ecography is a bimonthly peer-reviewed scientific journal published by Wiley-Blackwell on behalf of the Nordic Society Oikos covering the field of spatial ecology. It has been published since 1978, the first 14 volumes under the name Holarctic Ecology. Ecography is published in collaboration with Oikos, Journal of Avian Biology, Nordic Journal of Botany, Lindbergia, and with the monograph series Ecological Bulletins. It is available as an open-access publication via Wiley. According to the Journal Citation Reports, the journal has an impact factor of 6.45 as of 2019, ranking it 4th out of 59 journals in the category "Biodiversity Conservation" and twelve out of 165 journals in the category "Ecology".
academic journal | Q737498 |
open-access journal | Q773668 |
scientific journal | Q5633421 |
society journal | Q73364223 |
P6981 | ACNP journal ID | 2234567 |
915590 | ||
P1159 | CODEN | ECOGEG |
P8375 | Crossref journal ID | 3386 |
P1250 | Danish Bibliometric Research Indicator (BFI) SNO/CNO | 9665 |
P5115 | Directory of Open Access Journals ID | 1600-0587 |
P356 | DOI | 10.1111/(ISSN)1600-0587 |
P1058 | ERA Journal ID | 3227 |
P646 | Freebase ID | /m/02z4r4x |
P1160 | ISO 4 abbreviation | Ecography |
P236 | ISSN | 0906-7590 |
1600-0587 | ||
P7363 | ISSN-L | 0906-7590 |
P1230 | JSTOR journal ID | ecography |
P1277 | JUFO ID | 54961 |
P1144 | Library of Congress Control Number (LCCN) (bibliographic) | 92641619 |
P1055 | NLM Unique ID | 101187590 |
P243 | OCLC control number | 50102682 |
P856 | official website | http://www.wiley.com/bw/journal.asp?ref=0906-7590 |
P10283 | OpenAlex ID | S25093289 |
P3181 | OpenCitations bibliographic resource ID | 106569 |
P7461 | Publons journals/conferences ID | 990 |
P7662 | Scilit journal ID | 118591 |
P1156 | Scopus source ID | 20276 |
P12897 | Wiley Online Library journal ID | 16000587 |
P1240 | Danish Bibliometric Research Indicator level | 2 | |
P571 | inception | 1978-01-01 | |
P8875 | indexed in bibliographic review | Scopus | Q371467 |
Science Citation Index Expanded | Q104047209 | ||
P407 | language of work or name | English | Q1860 |
P921 | main subject | ecology | Q7150 |
P2284 | price | 1900 | |
P123 | publisher | Wiley-Blackwell | Q767319 |
P1476 | title | Ecography |
Q112569909 | 30% land conservation and climate action reduces tropical extinction risk by more than 50% |
Q126207364 | 6. Leaf sizes in Saussurea alpina along a dryâwet gradient and in artificially shaded Rubus chamaemorus plants |
Q121591382 | Linking species thermal tolerance to elevational range shifts in upland dung beetles |
Q125260864 | Revisitation analysis uncovers spatioâtemporal patterns in animal movement data |
Q126162274 | NâSDM: a highâperformance computing pipeline for Nested Species Distribution Modelling |
Q129106152 | climetrics: an R package to quantify multiple dimensions of climate change |
Q126265228 | A Great Escape: resource availability and densityâdependence shape population dynamics along trailing range edges |
Q112801065 | A Pleistocene disturbance event describes modern diversity patterns in tidal marsh birds |
Q58192963 | A balanced view of scale in spatial statistical analysis |
Q60353917 | A biogeographic reversal in sexual size dimorphism along a continental temperature gradient |
Q56422029 | A centroid model of species distribution with applications to the Carolina wrenThryothorus ludovicianusand house finchHaemorhous mexicanusin the United States |
Q56961247 | A century of failure for habitat recovery |
Q56964140 | A combination of functionally different plant traits provides a means to quantitatively predict a broad range of species assemblages in NW Europe |
Q60564548 | A common currency for the different ways in which patches and links can contribute to habitat availability and connectivity in the landscape |
Q122354720 | A comparative analysis of the habitat of the extinct aurochs and other prehistoric mammals in Britain |
Q111263761 | A comparative approach to understanding factors limiting abundance patterns and distributions in a fig tree-fig wasp mutualism |
Q60335853 | A comparative evaluation of pairwise nestedness measures |
Q112796941 | A comparative study of interspecific variation in fruit size among Australian eucalypts |
Q112796945 | A comparison of fine-scale distribution patterns of four plant groups in an Amazonian rainforest |
Q110762523 | A comprehensive examination of the network position hypothesis across multiple river metacommunities |
Q110626267 | A comprehensive formula for decomposing change in community similarity into introduction and extinction events |
Q60567372 | A continental-scale analysis of fish assemblage functional structure in European rivers |
Q114146139 | A crossâscale framework to support a mechanistic understanding and modelling of marine climateâdriven species redistribution, from individuals to communities |
Q112800960 | A dimmer shade of pale: revealing the faint signature of local assembly processes on the structure of strongly filtered plant communities |
Q30054430 | A diversity of beta diversities: straightening up a concept gone awry. Part 1. Defining beta diversity as a function of alpha and gamma diversity |
Q30051168 | A diversity of beta diversities: straightening up a concept gone awry. Part 2. Quantifying beta diversity and related phenomena |
Q125463799 | A facultative mutualism facilitates European seagrass meadows |
Q126920399 | A flexible framework to assess patterns and drivers of beta diversity across spatial scales |
Q125858246 | A food web perspective on large herbivore community limitation |
Q58319946 | A framework for evaluating the influence of climate, dispersal limitation, and biotic interactions using fossil pollen associations across the late Quaternary |
Q125908025 | A general metaâecosystem model to predict ecosystem functions at landscape extents |
Q114627642 | A global framework for linking alpineâtreeline ecotone patterns to underlying processes |
Q108805891 | A global perspective on the functional responses of stream communities to flow intermittence |
Q60140828 | A humped latitudinal phylogenetic diversity pattern of orchid bees (Hymenoptera: Apidae: Euglossini) in western Amazonia: assessing the influence of climate and geologic history |
Q115405584 | A largeâscale assessment of ant diversity across the Brazilian Amazon Basin: integrating geographic, ecological and morphological drivers of sampling bias |
Q130151692 | A latitudinal gradient in dimensionality of biodiversity |
Q122519508 | A latitudinal signal in the relationship between species geographic range size and climatic niche area |
Q29028150 | A local nearest-neighbor convex-hull construction of home ranges and utilization distributions |
Q112801028 | A macroecological approach to evolutionary rescue and adaptation to climate change |
Q56688723 | A meta-analysis of isolation by distance: relic or reference standard for landscape genetics? |
Q65555299 | A metabolic view of amphibian local community structure: the role of activation energy |
Q57239201 | A metacommunity-scale comparison of species-abundance distribution models for plant communities of eastern Australia |
Q110762748 | A metacommunity-scale comparison of species-abundance distribution models for plant communities of eastern Australia |
Q58208149 | A method to incorporate the effect of taxonomic uncertainty on multivariate analyses of ecological data |
Q128163368 | A mismatch between community assembly and abundanceâbased diversity indices |
Q125879286 | A multiâscale test for dispersal filters in an island plant community |
Q57205176 | A network approach for inferring species associations from co-occurrence data |
Q58312511 | A new method to infer vegetation boundary movement from âsnapshotâ data |
Q60532620 | A new non-parametric method for analyzing replicated point patterns in ecology |
Q57015584 | A novel framework for disentangling the scale-dependent influences of abiotic factors on alpine treeline position |
Q60297046 | A null-model for significance testing of presence-only species distribution models |
Q128785344 | A parsimonious view of the parsimony principle in ecology and evolution |
Q112796908 | A practical guide to MaxEnt for modeling species' distributions: what it does, and why inputs and settings matter |
Q56980656 | A predictive framework to assess spatio-temporal variability of infestations by the European spruce bark beetle |
Q112801012 | A processâbased model supports an association between dispersal and the prevalence of species traits in tropical reef fish assemblages |
Q125160263 | A protocol for reproducible functional diversity analyses |
Q112800940 | A quantitative review of abundanceâbased species distribution models |
Q56534699 | A re-examination of geographical variation in Nepenthes food webs |
Q54286065 | A recipe for scavenging in vertebrates - the natural history of a behaviour |
Q114146142 | A refined model of body mass and population density in flightless birds reconciles extreme bimodal population estimates for extinct moa |
Q103717806 | A rewilding agenda for Europe: creating a network of experimental reserves |
Q109585354 | A simple method to estimate the probable distribution of species |
Q118189365 | A simulation model of mire patterning - revisited |
Q58193609 | A spatial model of bird abundance as adjusted for detection probability |
Q57257395 | A species-centered approach for uncovering generalities in organism responses to habitat loss and fragmentation |
Q112800990 | A standard protocol for reporting species distribution models |
Q112800999 | A standardized assessment of forest mammal communities reveals consistent functional composition and vulnerability across the tropics |
Q57122295 | A systematic comparison of summary characteristics for quantifying point patterns in ecology |
Q121607059 | A test of the green wave hypothesis in omnivorous brown bears across North America |
Q113174634 | A trait-based framework for discerning drivers of species co-occurrence across heterogeneous landscapes |
Q60534170 | A unified index to measure ecological diversity and species rarity |
Q58321853 | A wavelet-based approach to evaluate the roles of structural and functional landscape heterogeneity in animal space use at multiple scales |
Q111663519 | A weighting method to improve habitat association analysis: tested on British carabids |
Q35564393 | ALADYN - a spatially explicit, allelic model for simulating adaptive dynamics |
Q118391138 | Abundance - occupancy relationships in macrofauna on exposed sandy beaches: patterns and mechanisms |
Q59116691 | Abundance and diversity of birch-feeding leafminers along latitudinal gradients in northern Europe |
Q112798865 | Abundance patterns and coexistence processes in communities of fleas parasitic on small mammals |
Q112800916 | Acaulescence promotes speciation and shapes the distribution patterns of palms in Neotropical seasonally dry habitats |
Q129607174 | Accessibility maps as a tool to predict sampling bias in historical biodiversity occurrence records |
Q56922818 | Accommodating scenarios of climate change and management in modelling the distribution of the invasive tree Schinus molle in South Africa |
Q57193930 | Accounting for data heterogeneity in patterns of biodiversity: an application of linear mixed effect models to the oceanic island biogeography of spore-producing plants |
Q114824051 | Accounting for imperfect detection in data from museums and herbaria when modeling species distributions: combining and contrasting dataâlevel versus modelâlevel bias correction |
Q56929415 | Accounting for imperfect observation and estimating true species distributions in modelling biological invasions |
Q112801015 | Accounting for longâterm directional trends on yearâtoâyear synchrony in species fluctuations |
Q57205196 | Accounting for spatial autocorrelation in null models of tree species association |
Q57257763 | Accounting for spatial pattern when modeling organism-environment interactions |
Q109746351 | Accounting for species interactions is necessary for predicting how arctic arthropod communities respond to climate change |
Q125028977 | Accounting for the topology of road networks to better explain humanâmediated dispersal in terrestrial landscapes |
Q56775150 | Accounting for uncertainty in colonisation times: a novel approach to modelling the spatio-temporal dynamics of alien invasions using distribution data |
Q120016259 | Accumulation and release of organic matter in ombrotrophic bog hummocks - processes and regional variation |
Q57050574 | Acido- and neutrophilic temperate forest plants display distinct shifts in ecological pH niche across north-western Europe |
Q112796971 | Activity patterns in moose and roe deer in a north boreal forest |
Q56286376 | Actual and potential tree-line in the North Atlantic region, especially in Greenland and the Faroes |
Q56004042 | Adaptive advantages of myrmecochory: the predator-avoidance hypothesis tested over a wide geographic range |
Q58716961 | Addressing common pitfalls does not provide more support to geographical and ecological abundant-centre hypotheses |
Q57122141 | Adopting a spatially explicit perspective to study the mysterious fairy circles of Namibia |
Q112796915 | Adult age of vascular plant species along an elevational landâuse and climate gradient |
Q128752389 | Aeroecology meets aviation safety: early warning systems in Europe and the Middle East prevent collisions between birds and aircraft |
Q130004192 | Afromontane understory birds increase in body size over four decades |
Q114080200 | Age-related change in canopy traits shifts conspecific facilitation to interference in a semi-arid shrubland |
Q111628459 | Agent-based model approach to optimal foraging in heterogeneous landscapes: effects of patch clumpiness |
Q56833087 | Aggregation and species coexistence in fleas parasitic on small mammals |
Q60525923 | Aggregations from using inadvertent social information: a form of ideal habitat selection |
Q106890202 | Agriculture rivals biomes in predicting global species richness |
Q112800977 | Agriâenvironment conservation setâasides have coâbenefits for connectivity |
Q112598721 | Airflow modelling predicts seabird breeding habitat across islands |
Q110626166 | Alien species richness is currently unbounded in all but the most urbanized bird communities |
Q117044787 | All that changes is not shift: methodological choices influence niche shift detection in freshwater invasive species |
Q57025868 | Allometric density responses in butterflies: the response to small and large patches by small and large species |
Q115405609 | Alpha and beta diversity of connected benthicâsubsurface invertebrate communities respond to drying in dynamic river ecosystems |
Q111492927 | Alteration of salt marsh plant community composition by grazing snow geese |
Q125723420 | Altered beta diversity in postâagricultural woodlands: two hypotheses and the role of scale |
Q62556948 | Alternative stable equilibria and critical thresholds created by fire regimes and plant responses in a fireâprone community |
Q114081982 | Altitudinal dispersal process drives community assembly of montane small mammals |
Q121335875 | Ambient ultraviolet-B radiation reduces hatchling size in the common frog Rana temporaria |
Q122226095 | Ambient ultraviolet-B radiation reduces hatchling size in the common frog Rana temporaria |
Q57199429 | Among-species overlap in rodent body size distributions predicts species richness along a temperature gradient |
Q112800945 | Amphibian diversity in the Amazonian floating meadows: a Hanski coreâsatellite species system |
Q57247407 | An ecological function in crisis? The temporal overlap between plant flowering and pollinator function shrinks as the Arctic warms |
Q110761664 | An ecoregionâbased approach to restoring the world's intact large mammal assemblages |
Q58005932 | An evaluation of transferability of ecological niche models |
Q60370171 | An evolutionary tolerance model explaining spatial patterns in species richness under environmental gradients and geometric constraints |
Q60503406 | An experimental test of frequency-dependent food selection: winter browsing by moose |
Q61465685 | An indirect area effect on elevational species richness patterns |
Q61465686 | An indirect area effect on elevational species richness patterns |
Q110762519 | An integrative framework of coexistence mechanisms in competitive metacommunities |
Q57000362 | An intraspecific application of the leaf-height-seed ecology strategy scheme to forest herbs along a latitudinal gradient |
Q60231651 | An update of the world survey of myrmecochorous dispersal distances |
Q60568993 | Analysis of determinants of mammalian species richness in South America using spatial autoregressive models |
Q123302775 | Anatomy of a cline: dissecting antiâpredatory adaptations in a marine gastropod along the U.S. Atlantic coast |
Q112801084 | Animal culture impacts species' capacity to realise climate-driven range shifts |
Q112801009 | Annual temperature variation influences the vulnerability of montane bird communities to landâuse change |
Q59546566 | Annual variation in long-distance dispersal driven by breeding and non-breeding season climatic conditions in a migratory bird |
Q110809103 | Anomalous outbreaks of an invasive defoliator and native bark beetle facilitated by warm temperatures, changes in precipitation and interspecific interactions |
Q56481234 | Ant mosaics occur in SE Asian oil palm plantation but not rain forest and are influenced by the presence of nest-sites and non-native species |
Q125567538 | Anthropogenic disturbance and rainfall variation threaten the stability of plantâant interactions in the Brazilian Caatinga |
Q61968773 | Anthropogenic disturbance changes the structure of arboreal tropical ant communities |
Q57615339 | Anthropogenic impacts weaken Bergmann's rule |
Q60541173 | Anthropogenic threats can have cascading homogenizing effects on the phylogenetic and functional diversity of tropical ecosystems |
Q35114152 | Anticipating the spatio-temporal response of plant diversity and vegetation structure to climate and land use change in a protected area |
Q60342699 | Applying species distribution models to caves and other subterranean habitats |
Q57038534 | Applying the dark diversity concept to plants at the European scale |
Q72995945 | Arctic arthropod assemblages in habitats of differing shrub dominance |
Q57198491 | Are Chaoborus larvae more abundant in acidified than in non-acidified lakes in Central Canada? |
Q60525563 | Are comparisons of species distribution models biased? Are they biologically meaningful? |
Q28649506 | Are different facets of plant diversity well protected against climate and land cover changes? A test study in the French Alps |
Q109351284 | Are forest birds categorised as âedge speciesâ strictly associated with edges? |
Q114082009 | Are forestâshrubland mosaics of the Cape Floristic Region an example of alternate stable states? |
Q111376365 | Are habitat islands islands? Woodliving beetles (Coleoptera) in deciduous forest fragments in boreal forest |
Q104206254 | Are island-like systems biologically similar to islands? A review of the evidence |
Q112796943 | Are islands more susceptible to be invaded than continents? Birds say no |
Q112796946 | Are macroinvertebrate communities influenced by seagrass structural complexity? |
Q58875728 | Are peripheral populations special? Congruent patterns in two butterfly species |
Q57269434 | Are protected areas maintaining bird diversity? |
Q60550065 | Are richness patterns of common and rare species equally well explained by environmental variables? |
Q58040606 | Are spatial regression methods a panacea or a Pandora's box? A reply to Beale et al. (2007) |
Q55842495 | Are there body size implications for the success of globally introduced land birds? |
Q111419027 | Are there saproxylic beetle species characteristic of high dead wood connectivity? |
Q111419387 | Are there saproxylic beetle species characteristic of high dead wood connectivity? |
Q55328258 | Are threat status and invasion success two sides of the same coin? |
Q125117006 | Area, altitude and aquatic plant diversity |
Q57273025 | Area-sensitivity by forest songbirds: theoretical and practical implications of scale-dependency |
Q114551993 | Aridity, soil and biome stability influence plant ecoregions in the Atlantic Forest, a biodiversity hotspot in South America |
Q115527975 | Artificial nest predation and habitat fragmentation: different trends in bird and mammal predators |
Q115527958 | Artificial nest predation rates in tropical and temperate forests: a review of the effects of edge and nest site |
Q107540487 | Artificial nightlight alters the predatorâprey dynamics of an apex carnivore |
Q111376460 | Aspen lichens in agricultural and forest landscapes: the importance of habitat quality |
Q56945723 | Assembly mechanisms determining high species turnover in aquatic communities over regional and continental scales |
Q112796913 | Assembly mechanisms shaping tropical litter ant communities |
Q56984095 | Assembly rules are rare in SE Australian bird communities, but sometimes apply in fragmented agricultural landscapes |
Q56832939 | Assembly rules of ectoparasite communities across scales: combining patterns of abiotic factors, host composition, geographic space, phylogeny and traits |
Q60561102 | Assessing among-lineage variability in phylogenetic imputation of functional trait datasets |
Q57197603 | Assessing completeness of biodiversity databases at different spatial scales |
Q56768722 | Assessing ecosystem threats from global and regional change: hierarchical modeling of risk to sagebrush ecosystems from climate change, land use and invasive species in Nevada, USA |
Q60388142 | Assessing five decades of change in a high Arctic parasitoid community |
Q112800965 | Assessing functional redundancy in Eurasian small mammal assemblages across multiple traits and biogeographic extents |
Q57005729 | Assessing habitat suitability for tiger in the fragmented Terai Arc Landscape of India and Nepal |
Q57179642 | Assessing spatial and environmental drivers of phylogenetic structure in BrazilianAraucariaforests |
Q110790431 | Assessing the accuracy of densityâindependent demographic models for predicting species ranges |
Q126841863 | Assessing the effectiveness of foraging radius models for seabird distributions using biotelemetry and survey data |
Q60566396 | Assessing the relationship between forest types and canopy tree beta diversity in Amazonia |
Q126209870 | Assessing the relative influences of abiotic and biotic factors on American eel Anguilla rostrata distribution using hydrologic, physical habitat, and functional trait data |
Q57730292 | Assessing the role of large herbivores in the structuring and functioning of freshwater and marine angiosperm ecosystems |
Q112605778 | Assessing the role of megafauna in tropical forest ecosystems and biogeochemical cycles - the potential of vegetation models |
Q125030177 | Assessing the spatial variability of density dependence in waterfowl populations |
Q100252553 | Assessing yearâround habitat use by migratory sea ducks in a multiâspecies context reveals seasonal variation in habitat selection and partitioning |
Q57532418 | Associations of garden birds with gradients in garden habitat and local habitat |
Q112800988 | Asymmetric response of forest and grassy biomes to climate variability across the African Humid Period: influenced by anthropogenic disturbance? |
Q60547499 | Asynchronous local dynamics contributes to stability of a seagrass bed in Tokyo Bay |
Q126863430 | At what spatial scale(s) do mammals respond to urbanization? |
Q112800917 | Automated synthesis of biodiversity knowledge requires better tools and standardised research output |
Q112798857 | Awesome or ordinary? Global diversity patterns of oribatid mites |
Q125423698 | BACKLAND: spatially explicit and highâresolution pollenâbased BACKward LANDâcover reconstructions |
Q129398512 | BBMV: an R package for the estimation of macroevolutionary landscapes |
Q57021233 | BIOMOD - a platform for ensemble forecasting of species distributions |
Q56079068 | Banksia pollen in the diet of Australian mammals |
Q59546499 | Barriers to salmon migration impact body condition, offspring size, and life history variation in an avian consumer |
Q56567752 | Bat species richness and abundance in tropical rain forest fragments and in agricultural habitats at Los Tuxtlas, Mexico |
Q60550689 | Bayesian clustering with AutoClass explicitly recognises uncertainties in landscape classification |
Q56817123 | Bayesian image restoration models for combining expert knowledge on recording activity with species distribution data |
Q111376356 | Beetle diversity in a matrix of old-growth boreal forest: influence of habitat heterogeneity at multiple scales |
Q124694623 | Beetle evolution illuminates the geological history of the World's most diverse tropical archipelago |
Q109351285 | Beetle species richness along the forest productivity gradient in northern Finland |
Q112801010 | Behavior influences range limits and patterns of coexistence across an elevational gradient in tropical birds |
Q115533034 | Behavioral response of a mobile marine predator to environmental variables differs across ecoregions |
Q105952524 | Behavioural mechanisms that undermine species envelope models: the causes of patchiness in the distribution of great bustards Otis tarda in Spain |
Q114625064 | Benthic resting periods of pelagic cyclopoids in an oligotrophic lake |
Q62564296 | Bergmann's rule in alien birds |
Q60488125 | Beta diversity of rock-restricted cichlid fishes in Lake Malawi: importance of environmental and spatial factors |
Q63487063 | Beta-diversity of central European forests decreases along an elevational gradient due to the variation in local community assembly processes |
Q57230218 | Beyond bioclimatic envelopes: dynamic species' range and abundance modelling in the context of climatic change |
Q58388927 | BioMove - an integrated platform simulating the dynamic response of species to environmental change |
Q57248714 | Biocomplexity in large tree mortality: interactions between elephant, fire and landscape in an African savanna |
Q58046502 | Biodiverse, a tool for the spatial analysis of biological and related diversity |
Q58205839 | Biodiversity and biogeography of Southern Ocean pycnogonids |
Q108426649 | Biodiversity dynamics in the Anthropocene: how human activities change equilibria of species richness |
Q63564818 | Biodiversity extinction thresholds are modulated by matrix type |
Q63389792 | Biodiversity growth on the volcanic ocean islands and the roles of in situ cladogenesis and immigration: case with the reptiles |
Q112796952 | Biodiversity indicators: graphical techniques, smoothing and searching for what makes relationships work |
Q56984239 | Biogeo: an R package for assessing and improving data quality of occurrence record datasets |
Q112798864 | Biogeographic, environmental, and phylogenetic influences on reproductive traits in subtropical forest trees, South Africa |
Q56550424 | Biogeographical contrasts to assess local and regional patterns of invasion: a case study with two reciprocally introduced exotic maple trees |
Q55841888 | Biogeographical regions of the Iberian peninsula based on freshwater fish and amphibian distributions |
Q125262552 | Biogeography of Lacerta (Zootoca) vivipara: reproductive mode and enzyme phenotypes in Bulgaria |
Q113798979 | Biogeography of bird and mammal trophic structures |
Q59266114 | Biogeography of body size in Pacific island birds |
Q57061927 | Biogeography of boreal passerine range dynamics in western North America: past, present, and future |
Q58657026 | Biogeography of parasitism in freshwater fish: spatial patterns in hot spots of infection |
Q125756777 | Biogeography of telomere dynamics in a vertebrate |
Q56380608 | Biological invasion hotspots: a trait-based perspective reveals new sub-continental patterns |
Q55842497 | Biological invasions of Southern Ocean islands: the Collembola of Marion Island as a test of generalities |
Q114080274 | Biological invasions of Southern Ocean islands: the Collembola of Marion Island as a test of generalities |
Q60561497 | Biological trait composition of European stream invertebrate communities: assessing the effects of various trait filter types |
Q120016279 | Biomass, productivity and relative rate of photosynthesis of Sphagnum at different water levels on a South Swedish peat bog |
Q57976322 | Biome transitions as centres of diversity: habitat heterogeneity and diversity patterns of West African bat assemblages across spatial scales |
Q111289077 | Biotic and abiotic interactions between surface and interstitial systems in rivers |
Q57014042 | Biotic and abiotic variables show little redundancy in explaining tree species distributions |
Q113087415 | Biotic homogenization increases with human intervention: implications for mangrove wetland restoration |
Q111172413 | Biotic homogenization of oceanic islands depends on taxon, spatial scale and the quantification approach |
Q57269860 | Biotic interactions affect the elevational ranges of high-latitude plant species |
Q57013825 | Biotic interactions boost spatial models of species richness |
Q110762530 | Biotic interactions hold the key to understanding metacommunity organisation |
Q124840312 | Biotic predictors with phenological information improve range estimates for migrating monarch butterflies in Mexico |
Q56518977 | Biotic responses of canids to the terminal Pleistocene megafauna extinction |
Q114625042 | Bird species turnover and stochastic extinction in woodland fragments |
Q58170413 | Bison extirpation may have caused aspen expansion in western Canada |
Q112800984 | Blind assessment of vertebrate taxonomic diversity across spatial scales by clustering environmental DNA metabarcoding sequences |
Q114144824 | Body mass and winter mortality in red deer calves: disentangling sex and climate effects |
Q115405605 | Body massârelated changes in mammal community assembly patterns during the late Quaternary of North America |
Q60513410 | Body morphology of crucian carp Carassius carassius in lakes with or without piscivorous fish |
Q60459034 | Body size - prey size relationships in European stoats Mustela erminea: a test case |
Q57068830 | Body size determines the strength of the latitudinal diversity gradient |
Q61887146 | Body size trends in a Holocene island bird assemblage |
Q125102706 | Body size varies with abundance, not climate, in an amphibian population |
Q58510284 | Botanical richness and endemicity patterns of Borneo derived from species distribution models |
Q112800925 | Both sourceâ and recipientârange phylogenetic community structure can predict the outcome of avian introductions |
Q112801112 | Both traits and phylogenetic history influence community structure in snakes over steep environmental gradients |
Q115527509 | Bottom-up and top-down processes in African ungulate communities: resources and predation acting on the relative abundance of zebra and grazing bovids |
Q58192703 | Box-Cox-chord transformations for community composition data prior to beta diversity analysis |
Q113298187 | Breaking down the barrier: dispersal across the Antarctic Polar Front |
Q125634568 | Breeding bird dynamics in a primaeval temperate forest: longâterm trends in Biatowieza National Park (Poland) |
Q63627821 | Breeding bird species diversity across gradients of land use from forest to agriculture in Europe |
Q114627162 | Breeding bird species richness in Spain: assessing diversity hypothesis at various scales |
Q59154359 | Breeding dynamics of Triturus carnifex at a pond in northwestern Italy (Amphibia, Urodela, Salamandridae) |
Q57065239 | Breeding like rabbits: global patterns of variability and determinants of European wild rabbit reproduction |
Q112801036 | Bringing Elton and Grinnell together: a quantitative framework to represent the biogeography of ecological interaction networks |
Q59392496 | Broad-scale biodiversity pattern of the endemic tree flora of the Western Ghats (India) using canonical correlation analysis of herbarium records |
Q58942488 | Broad-scale geographic patterns in body size and hind wing development of western Palaearctic carabid beetles(Coleoptera: Carabidae) |
Q54647019 | Brood care in the dung beetle Onthophagus vacca (Coleoptera: Scarabaeidae): the effect of soil moisture on time budget, nest structure, and reproductive success |
Q112796947 | Browsing in a heterogeneons savanna |
Q28658248 | Building megaphylogenies for macroecology: taking up the challenge |
Q127658481 | Bunching up the background betters bias in species distribution models |
Q57706984 | Butterfly dispersal across Amazonia and its implication for biogeography |
Q60362619 | Butterfly species differing in mobility show different structures of dispersal-related syndromes in the same fragmented landscape |
Q58195618 | Butterfly species richness in mainland Portugal: predictive models of geographic distribution patterns |
Q125727462 | Calculating functional diversity metrics using neighborâjoining trees |
Q58380816 | Can antibrowsing defense regulate the spread of woody vegetation in arctic tundra? |
Q54802711 | Can biotic interactions cause allopatry? Niche models, competition, and distributions of South American mouse opossums |
Q60550059 | Can collective memories shape fish distributions? A test, linking space-time occurrence models and population demographics |
Q114946644 | Can inconspicuous legumes facilitate alien grass invasions? Partridge peas and fountain grass in Hawaiâi |
Q58108450 | Can models of presence-absence be used to scale abundance? Two case studies considering extremes in life history |
Q57062817 | Can patterns of spatial autocorrelation reveal population processes? An analysis with the fire salamander |
Q112595085 | Can site and landscape-scale environmental attributes buffer bird populations against weather events? |
Q112796919 | Can species distribution models be used to describe plant abundance patterns? |
Q60283236 | Can we predict butterfly diversity along an elevation gradient from space? |
Q130073863 | Canadian butterfly climate debt is significant and correlated with range size |
Q60390929 | Canopy insect herbivores in the Azorean Laurisilva forests: key host plant species in a highly generalist insect community |
Q126646419 | Capturing juvenile tree dynamics from count data using Approximate Bayesian Computation |
Q60567155 | CarboScen: a tool to estimate carbon implications of land-use scenarios |
Q114146157 | Carnivoran postcranial adaptations and their relationships to climate |
Q60317148 | Caterpillars on the run â induced defences create spatial patterns in host plant damage |
Q60317161 | Caterpillars on the run â induced defences create spatial patterns in host plant damage |
Q60570914 | Caught in the mesh: roads and their network-scale impediment to animal movement |
Q60147835 | Celebrating the diversity of biogeographical research |
Q114081981 | Chameleon biogeographic dispersal is associated with extreme life history strategies |
Q112796924 | Change in community phylogenetic structure during tropical forest succession: evidence from New Guinea |
Q56936914 | Change within and among forest communities: the influence of historic disturbance, environmental gradients, and community attributes |
Q113794786 | Changes in Danish farmland habitats and their populations of breeding birds |
Q112814401 | Changes in carabid beetle assemblages across an urban-rural gradient in Japan |
Q55842080 | Changes in community and population responses across a forest-field gradient |
Q115533039 | Changes in desert avifauna associated with the functional extinction of a terrestrial top predator |
Q114144822 | Changes in fish condition and mercury vary by region, notBythotrephesinvasion: a result of climate change? |
Q60458796 | Changes in life-history traits in an expanding moss species: phenotypic plasticity or genetic differentiation? A reciprocal transplantation experiment withPogonatum dentatum |
Q56768717 | Changes in non-randomness in the expanding introduced avifauna of the world |
Q126020959 | Changes in potential habitat of 147 North American breeding bird species in response to redistribution of trees and climate following predicted climate change |
Q110757154 | Changes in seed predation along a 2300âm elevational gradient on a tropical mountain in Myanmar: a standardized test with 32 nonânative plant species |
Q56827812 | Changes in species' distributions during and after environmental change: which eco-evolutionary processes matter more? |
Q114146093 | Changes in the climate suitability and growth rates of trees in eastern North America |
Q112603439 | Changing fish distributions challenge the effective management of European fisheries |
Q58404771 | Characterising the temporal variability of the spatial distribution of animals: an application to seabirds at sea |
Q122979341 | Characteristics of fleshy fruits in southeast Alaska: phylogenetic comparison with fruits from Illinois |
Q110625828 | Characteristics of the naturalized flora of Southern Africa largely reflect the nonârandom introduction of alien species for cultivation |
Q104205923 | Chironomid communities as water quality indicators |
Q120016280 | Chironomidae (Diptera) of peatlands in northwestern Ontario, Canada |
Q112796969 | Choice of feeding sites by moose during summer, the influence of forest structure and plant phenology |
Q113798982 | CircumâArctic distribution of chemical antiâherbivore compounds suggests biomeâwide tradeâoff in defence strategies in Arctic shrubs |
Q125420306 | Citizen science data reveal altitudinal movement and seasonal ecosystem use by hummingbirds in the Andes Mountains |
Q112607854 | Clade-specific consequences of climate change to amphibians in Atlantic Forest protected areas |
Q60480225 | Classical metapopulation dynamics and eco-evolutionary feedbacks in dendritic networks |
Q60561103 | Climate and amphibian body size: a new perspective gained from the fossil record |
Q112800910 | Climate and landâuse driven reorganisation of structure and function in river macroinvertebrate communities |
Q57062075 | Climate and vegetation hierarchically structure patterns of songbird distribution in the Canadian boreal region |
Q57194064 | Climate and woody plant diversity in southern Africa: relationships at species, genus and family levels |
Q28608480 | Climate as a driver of tropical insular diversity: comparative phylogeography of two ecologically distinctive frogs in Puerto Rico |
Q112801017 | Climate change and the future restructuring of Neotropical anuran biodiversity |
Q56477330 | Climate change could alter the distribution of mountain pine beetle outbreaks in western Canada |
Q57904407 | Climate change may drive cave spiders to extinction |
Q58387984 | Climate change reduces genetic diversity of Canada lynx at the trailing range edge |
Q58728474 | Climate change shifts environmental space and limits transferability of treeline models |
Q114627649 | Climate change, glacier retreat and a new ice-free island offer new insights on Antarctic benthic responses |
Q57249321 | Climate drivers of bark beetle outbreak dynamics in Norway spruce forests |
Q112801027 | Climate effects on fish body sizeâtrophic position relationship depend on ecosystem type |
Q112800968 | Climate extreme variables generated using monthly timeâseries data improve predicted distributions of plant species |
Q63627849 | Climate induced changes in matrix suitability explain gene flow in a fragmented landscape - the effect of interannual rainfall variability |
Q112800957 | Climate influences the response of community functional traits to local conditions in bromeliad invertebrate communities |
Q60339025 | Climate interacts with anthropogenic drivers to determine extirpation dynamics |
Q112801019 | Climate limitation at the cold edge: contrasting perspectives from species distribution modelling and a transplant experiment |
Q60547035 | Climate refugia and migration requirements in complex landscapes |
Q67230775 | Climate-associated tundra thaw pond formation and range expansion of boreal zooplankton predators |
Q57013992 | Climate-based empirical models show biased predictions of butterfly communities along environmental gradients |
Q61790476 | Climate-mediated habitat selection in an arboreal folivore |
Q57068015 | Climate-related range shifts - a global multidimensional synthesis and new research directions |
Q112801014 | Climateâdriven shifts in the distribution of koalaâbrowse species from the Last Interglacial to the near future |
Q113272087 | Climateâinformed models benefit hindcasting but present challenges when forecasting speciesâhabitat associations |
Q127906140 | Climateâniche factor analysis: a spatial approach to quantifying species vulnerability to climate change |
Q60583452 | Climatic adaptation in an isolated and genetically impoverished amphibian population |
Q126650921 | Climatic and edaphic gradients predict variation in wildland fuel hazard in southâeastern Australia |
Q104638970 | Climatic and trophic processes drive long-term changes in functional diversity of freshwater invertebrate communities |
Q106620238 | Climatic aridity increases temporal nestedness of invertebrate communities in naturally drying rivers |
Q112800912 | Climatic conditions and functional traits affect spider diets in agricultural and nonâagricultural habitats worldwide |
Q112801073 | Climatic microrefugia under anthropogenic climate change: implications for species redistribution |
Q57981566 | Climatic thresholds shape northern high-latitude fire regimes and imply vulnerability to future climate change |
Q111172404 | Clustered or scattered? The impact of habitat quality clustering on establishment and early spread |
Q56936942 | Coefficient shifts in geographical ecology: an empirical evaluation of spatial and non-spatial regression |
Q125782575 | Cold and hungry: combined effects of low temperature and resource scarcity on an edgeâofârange temperate primate, the golden snubânose monkey |
Q56923875 | Collinearity: a review of methods to deal with it and a simulation study evaluating their performance |
Q114082007 | Colonisation dynamics during range expansion is poorly predicted by dispersal in the core range |
Q112796955 | Colonization dynamics and relative abundance of three plant species (Antennaria dioica, Hieradum pilosella and Hypochoeris maculata) in dry semi-natural grasslands |
Q57043652 | Colonization of new host plant individuals by locally adapted thrips |
Q56948492 | Colonization of the GalĂĄpagos Islands by plants with no specific syndromes for long-distance dispersal: a new perspective |
Q125030258 | Colonizing polar environments: thermal niche evolution in Collembola |
Q56211557 | Combination of humans, climate, and vegetation change triggered Late Quaternary megafauna extinction in the Ăltima Esperanza region, southern Patagonia, Chile |
Q56884445 | Combining information from range use and habitat selection: sex-specific spatial responses to habitat fragmentation in tawny owls Strix aluco |
Q112796939 | Combining plant and animal traits to assess community functional responses to disturbance |
Q111172495 | Combining species distribution models and population genomics underlines the determinants of range limitation in an emerging parasite |
Q58388049 | Comment on âMethods to account for spatial autocorrelation in the analysis of species distributional data: a reviewâ |
Q58424565 | Common and rare species respond to similar niche processes in macroinvertebrate metacommunities |
Q57615619 | Commonness patterns and the size of the species pool along a tropical elevational gradient: insights using a new quantitative tool |
Q57191252 | Community assembly is a race between immigration and adaptation: eco-evolutionary interactions across spatial scales |
Q125338418 | Community assembly processes and drivers shaping marine fish community structure in the North Sea |
Q115405618 | Community assembly processes restrict the capacity for genetic adaptation under climate change |
Q57193774 | Community functional trait composition at the continental scale: the effects of non-ecological processes |
Q114649178 | Community structure of ectomycorrhizal fungi across an alpine/subalpine ecotone |
Q57195182 | Community trait response to environment: disentangling species turnover vs intraspecific trait variability effects |
Q57021100 | Community-level vs species-specific approaches to model selection |
Q111376368 | Comparative analysis of temporal and spatial variability in above-ground production in a deciduous forest and prairie |
Q112801086 | Comparing macroecological patterns across continents: evolution of climatic niche breadth in varanid lizards |
Q56766290 | Comparing methods for measuring the rate of spread of invading populations |
Q56747591 | Comparing short and long-distance dispersal: modelling and field case studies |
Q114624990 | Comparing survival among species with imperfect detection using multilevel analysis of mark-recapture data: a case study on bats |
Q56968839 | Comparison of approaches to combine species distribution models based on different sets of predictors |
Q56456287 | Comparison of native and exotic distribution and richness models across scales reveals essential conservation lessons |
Q56949200 | Competition, facilitation and environmental severity shape the relationship between local and regional species richness in plant communities |
Q115532211 | Competition, predation and interspecific synchrony in cyclic small mammal communities |
Q57267224 | Complementarity of epi- and endozoochory of plant seeds by free ranging donkeys |
Q111172459 | Complementary strengths of spatiallyâexplicit and multiâspecies distribution models |
Q125405282 | Completeness analysis for over 3000 United States bee species identifies persistent data gap |
Q59139492 | Complex migration and the development of genetic structure in subdivided populations: an example from Caribbean coral reef ecosystems |
Q112801116 | Complex organism-environment feedbacks buffer species diversity against habitat fragmentation |
Q113174630 | Complex patterns of temperature sensitivity, not ecological traits, dictate diverse species responses to climate change |
Q114081998 | Complex relationships between beta diversity and dispersal in metaâcommunity models |
Q110704742 | Composition and viability of the seed bank along a successional gradient on a Baltic sea shore meadow |
Q114081996 | Comprehensive analytical approaches reveal speciesâspecific search strategies in sympatric apex predatory sharks |
Q58192965 | Conceptual and mathematical relationships among methods for spatial analysis |
Q57615645 | Congruence between floristic patterns of trees and lianas in a southwest Amazonian rain forest |
Q112798850 | Congruence between floristic patterns of trees and lianas in a southwest Amazonian rain forest |
Q118114469 | Connectance and parasite diet breadth in flea-mammal webs |
Q57428746 | Connecting models, data, and concepts to understand fragmentation's ecosystem-wide effects |
Q60314650 | Connectivity conservation priorities for individual patches evaluated in the present landscape: how durable and effective are they in the long term? |
Q113345347 | Consequences of dispersal for the quantitative study of adaptation in small-scale plots: a case study of an avian island population |
Q113349033 | Consequences of dispersal for the quantitative study of adaptation in small-scale plots: a case study of an avian island population |
Q59835702 | Consequences of ignoring spatial variation in population trend when conducting a power analysis |
Q107016637 | Conservation implications of the refugee species concept and the European bison: king of the forest or refugee in a marginal habitat? |
Q61360151 | Conservation paleobiogeography: the past, present and future of species distributions |
Q57218028 | Conservation paleobiology needs phylogenetic methods |
Q57209850 | Conservation planning with insects at three different spatial scales |
Q111376355 | Conservation value of secondary forest habitats for endemic birds, a perspective from two widely separated tropical ecosystems |
Q118114495 | Conservatism of host specificity in parasites |
Q60367796 | Considerations for the use of SADIE statistics to quangify spatial patterns |
Q67237481 | Consistent spatial patterns across biogeographic gradients in temperate reef fishes |
Q60561125 | Contemporary richness of holarctic trees and the historical pattern of glacial retreat |
Q63388234 | Contemporary richness of holarctic trees and the historical pattern of glacial retreat |
Q125972605 | Contents of Vol. 18 |
Q57039741 | Context-dependent interplays between truncated demographies and climate variation shape the population growth rate of a harvested species |
Q111289103 | Contextâdependent biotic interactions control plant abundance across altitudinal environmental gradients |
Q58195432 | Continent-level drivers of African pyrodiversity |
Q112800980 | Continentalâscale 1 km hummingbird diversity derived from fusing point records with lateral and elevational expert information |
Q112800931 | Continentalâscale shifts in termite diversity and nesting and feeding strategies |
Q114298744 | Continentâscale phenotype mapping using citizen scientistsâ photographs |
Q57004474 | Contingent absences account for range limits but not the local abundance structure of an invasive springtail |
Q60569297 | Continuum or discrete patch landscape models for savanna birds? Towards a pluralistic approach |
Q60322966 | Contrasting age-specific recruitment and survival at different spatial scales: a case study with the European storm petrel |
Q128365198 | Contrasting drivers of aboveground woody biomass and aboveground woody productivity in lowland forests of Colombia |
Q125407931 | Contrasting effects of beekeeping and land use on plantâpollinator networks and pathogen prevalence in Mediterranean semiarid ecosystems |
Q57207985 | Contrasting effects of different landscape characteristics on population growth of a perennial forest herb |
Q57001749 | Contrasting effects of habitat area and connectivity on evenness of pollinator communities |
Q112801061 | Contrasting effects of mosaic structure on alpha and beta diversity of bird assemblages in a humanâmodified landscape |
Q56962703 | Contrasting environmental and regional effects on global pteridophyte and seed plant diversity |
Q84967191 | Contrasting patterns of diversification in a bird family (Aves: Gruiformes: Rallidae) are revealed by analysis of geospatial distribution of species and phylogenetic diversity |
Q60533880 | Contrasting patterns of lichen functional diversity and species richness across an elevation gradient |
Q60486849 | Contrasting trait assembly patterns in plant and bird communities along environmental and human-induced land-use gradients |
Q57206399 | Controls over reproductive phenology among ungulates: allometry and tropical-temperate contrasts |
Q57030256 | Convergence of temperate and tropical stream fish assemblages |
Q115533049 | Coping with fast climate change in northern ecosystems: mechanisms underlying the population-level response of a specialist avian predator |
Q118134504 | Could ecologists be more random? Straightforward alternatives to haphazard spatial sampling |
Q115405593 | Coupled effects of environment, space and ecological engineering on seafloor betaâdiversity |
Q128943720 | Coupled land use and ecological models reveal emergence and feedbacks in socioâecological systems |
Q113798983 | Coupling ecoâevolutionary mechanisms with deepâtime environmental dynamics to understand biodiversity patterns |
Q60147998 | Cross-species and assemblage-based approaches to Bergmann's rule and the biogeography of body size in Plethodon salamanders of eastern North America |
Q57019729 | Cross-validation strategies for data with temporal, spatial, hierarchical, or phylogenetic structure |
Q129044701 | Crossâcalibration of different radar systems for monitoring nocturnal bird migration across Europe and the Near East |
Q112801003 | Crossâscale drivers of plant trait distributions in a fragmented forest landscape |
Q57227300 | Cryptic matters: overlooked species generate most butterfly beta-diversity |
Q111172440 | Current and projected future risks of freshwater fish invasions in China |
Q57038542 | Dark diversity in dry calcareous grasslands is determined by dispersal ability and stress-tolerance |
Q110762527 | Darwin's finches: a model of landscape effects on metacommunity dynamics in the GalĂĄpagos Archipelago |
Q28659831 | Darwin's naturalization hypothesis: scale matters in coastal plant communities |
Q126310706 | Dealing with areaâtoâpoint spatial misalignment in species distribution models |
Q57124025 | Dealing with virtual aggregation - a new index for analysing heterogeneous point patterns |
Q61465217 | Declining diversity and abundance of High Arctic fly assemblages over two decades of rapid climate warming |
Q56533559 | Decreased resistance and increased tolerance to native herbivores of the invasive plantSapium sebiferum |
Q59200123 | Deep-sea nematode biodiversity in the Mediterranean basin: testing for longitudinal, bathymetric and energetic gradients |
Q60529776 | Defaunation and fragmentation erode small mammal diversity dimensions in tropical forests |
Q125845340 | Demographic responses of arctic hares Lepus arcticus placed on two predominantly forested islands in Newfoundland |
Q117012610 | Demographic shifts in eastern US forests increase the impact of lateâseason drought on forest growth |
Q112605465 | Demographics in an alpine reindeer herd: effects of density and winter weather |
Q57060249 | Demography as the basis for understanding and predicting range dynamics |
Q57003844 | Demography of alpine red squirrel populations in relation to fluctuations in seed crop size |
Q111172528 | Density dependence and spatial heterogeneity limit the population growth rate of invasive pines at the landscape scale |
Q110790963 | Density dependence in forests is stronger in tropical and subtropical climates among closely related species |
Q115533041 | Density dependence, prey accessibility and prey depletion by fisheries drive Peruvian seabird population dynamics |
Q60510858 | Density-dependent dispersal and the formation of range borders |
Q112800973 | Deriving siteâspecific species pools from large databases |
Q56431689 | Detecting decline in a formerly widespread species: how common is the common blue butterfly Polyommatus icarus? |
Q56879802 | Detecting spatial patterns in species composition with multiple plot similarity coefficients and singularity measures |
Q57017795 | Determinants of data deficiency in the impacts of alien bird species |
Q57068391 | Determinants of palm species distributions across Africa: the relative roles of climate, non-climatic environmental factors, and spatial constraints |
Q112801048 | Determinants of reef fish assemblages in tropical Oceanic islands |
Q56991150 | Determinants of species richness in generalist and specialist Mediterranean butterflies: the negative synergistic forces of climate and habitat change |
Q57205121 | Determinants of species richness, endemism and turnover in European longhorn beetles |
Q57520022 | Determinants of tapeworm species richness in elasmobranch fishes: untangling environmental and phylogenetic influences |
Q115527512 | Determining prey distribution patterns from stomach-contents of satellite-tracked high-predators of the Southern Ocean |
Q57517297 | Determinism of bacterial metacommunity dynamics in the southern East China Sea varies depending on hydrography |
Q115527986 | Development of empirical feeding models for a benthic predator |
Q57050432 | Dialects of an invasive songbird are preserved in its invaded but not native source range |
Q115034306 | Diaspore traits specialized to animal adhesion and sea current dispersal are positively associated with the naturalization of European plants across the world |
Q59199702 | Diatom, chrysophyte and protozoan distributions along a latitudinal transect in Fennoscandia |
Q56225924 | Diet of the golden eagle Aquila chrysaetos during the breeding season in Sweden |
Q113794778 | Diet selection by vertebrate herbivores in the high arctic of Greenland |
Q121826643 | Diet variation of common buzzards in Finland supports the alternative prey hypothesis |
Q111376240 | Differences in litter mass change mite assemblage structure on a deciduous forest floor |
Q113172352 | Differences in spatial predictions among species distribution modeling methods vary with species traits and environmental predictors |
Q125286181 | Differences in spatial synchrony and interspecific concordance inform guildâlevel population trends for aerial insectivorous birds |
Q112796942 | Differences in species richness and life-history traits between grazed and abandoned grasslands in southern Sweden |
Q113182426 | Differences in species richness and life-history traits between grazed and abandoned grasslands in southern Sweden |
Q115527984 | Differences in uptake of persistent pollutants for predators feeding in aquatic and terrestrial habitats |
Q57267302 | Differential colonization causing non-random forest plant community structure in a fragmented agricultural landscape |
Q57267304 | Differential colonization causing non-random forest plant community structure in a fragmented agricultural landscape |
Q56836380 | Differential drift and parasitism in invading and nativeGammarusspp. (Crustacea: Amphipoda) |
Q59221981 | Differential establishment potential of species predicts a shift in coral assemblage structure across a biogeographic barrier |
Q60141422 | Differential response to abiotic conditions and predation risk rather than competition avoidance determine breeding site selection by anurans |
Q59884667 | Differential response to abiotic stress controls species distributions at biogeographic transition zones |
Q60390869 | Differential temporal beta-diversity patterns of native and non-native arthropod species in a fragmented native forest landscape |
Q60583411 | Differentiation in adaptive traits between neighbouring bog and mineral soil populations of Scots pine Pinus sylvestris |
Q55842305 | Direct and indirect effects of the introduced toad Bufo marinus (Anura: Bufonidae) on populations of native anuran larvae in Australia |
Q125357243 | Direct evidence for intercontinental dispersal of a snail via a bird |
Q58822064 | Direct negative density-dependence in a pond-breeding frog population |
Q28655265 | Directional biases in phylogenetic structure quantification: a Mediterranean case study |
Q113108762 | Discovering biogeographic and ecological clusters with a graph theoretic spin on factor analysis |
Q56067451 | Disease and the devil: density-dependent epidemiological processes explain historical population fluctuations in the Tasmanian devil |
Q58104610 | Disease ontogeny overshadows effects of climate and species interactions on population dynamics in a nonnative forest disease complex |
Q111289104 | Disentangling biotic interactions, environmental filters, and dispersal limitation as drivers of species co-occurrence |
Q57068702 | Disentangling distance decay of similarity from richness gradients: response to Baselga (2007) |
Q57205125 | Disentangling distance decay of similarity from richness gradients: response to Soininen et al. 2007 |
Q128815586 | Disentangling elevational richness: a multiâscale hierarchical Bayesian occupancy model of Colorado ant communities |
Q63389636 | Disentangling good from bad practices in the selection of spatial or phylogenetic eigenvectors |
Q57199889 | Disentangling regional and local tree diversity in the Amazon |
Q112801069 | Disentangling scale dependencies in species environmental niches and distributions |
Q57232169 | Disentangling spatio-temporal processes in a hierarchical system: a case study in fisheries discards |
Q60441138 | Disentangling the effects of spring anomalies in climate and net primary production on body size of temperate songbirds |
Q55056301 | Disentangling the pathways of land use impacts on the functional structure of fish assemblages in Amazon streams. |
Q112800976 | Disparate dispersal limitation inGeomalacusslugs unveiled by the shape and slope of the geneticâspatial distance relationship |
Q60361875 | Dispersal and alternative breeding site fidelity strategies in an amphibian |
Q112814409 | Dispersal and life span spectra in plant communities: a key to safe site dynamics, species coexistence and conservation |
Q56047478 | Dispersal and the metapopulation paradigm in amphibian ecology and conservation: are all amphibian populations metapopulations? |
Q110775517 | Dispersal modes affect tropical forest assembly across trophic levels |
Q112796965 | Dispersal strategies of Danish seashore plants |
Q115405602 | Dispersalâniche continuum index: a new quantitative metric for assessing the relative importance of dispersal versus niche processes in community assembly |
Q60147836 | Dispersion fields, diversity fields and null models: uniting range sizes and species richness |
Q60441460 | Distance decay of similarity in temperate aquatic communities: effects of environmental transition zones, distance measure, and life histories |
Q60394499 | Distance decay of similarity, effects of environmental noise and ecological heterogeneity among species in the spatio-temporal dynamics of a dispersal-limited community |
Q112798868 | Distinct patterns in alpine vegetation around dens of the Arctic fox |
Q126094002 | Distribution and abundance of butterflies in a mountain area in the northern Iberian peninsula |
Q121463036 | Distribution and abundance of tree species in swamp forests of Amazonian Ecuador |
Q114625040 | Distribution and dynamics of surface-dwelling spiders across a pasture-plantation ecotone |
Q114649177 | Distribution and habitat specialization of species affect local extinction in dragonfly Odonata populations |
Q111376361 | Distribution of birds in natural landscape mosaics of old-growth forests in northern Sweden: relations to habitat area and landscape context |
Q58193856 | Distribution of invasive and native riparian woody plants across the western USA in relation to climate, river flow, floodplain geometry and patterns of introduction |
Q125911467 | Distribution patterns of Cladocera in subarctic Fennoscandian lakes and their potential in environmental reconstruction |
Q57208065 | Distribution patterns of vascular plants in lakes - the role of metapopulation dynamics |
Q120016379 | Distribution, abundance and species associations of earthworms (Lumbricidae) in a reclaimed peat soil in Ireland |
Q112796415 | Distribution, abundance, and individual strategies: a multi-scale analysis of dasyurid marsupials in arid central Australia |
Q57245807 | Distributional niche of relatively rare sable antelope in a South African savanna: habitat versus biotic relationships |
Q60463547 | Distributions of forest birds and butterflies in the Andaman islands, Bay of Bengal: nested patterns and processes |
Q115405587 | Disturbanceâdriven alteration of patch connectivity determines local biodiversity recovery within metacommunities |
Q112800920 | Divergent occurrences of juvenile and adult trees are explained by both environmental change and ontogenetic effects |
Q58672083 | Diversification and biodiversity dynamics of hot and cold spots |
Q114930046 | Diversity and abundance patterns of phytophagous insect communities on alien and native host plants in the Brassicaceae |
Q112796967 | Diversity and evenness of Hemiptera communities on naturally vegetated derelict land in NW England |
Q114146129 | Diversity and phylogenetic community structure across elevation during climate change in a family of hyperdiverse neotropical beetles (Staphylinidae) |
Q125129999 | Diversity and specialization responses to climate and land use differ between deadwood fungi and bacteria |
Q122212770 | Diversity and structure of turtle assemblages: associations with wetland characters across a floodplain landscape |
Q122585316 | Diversity â volume relationships: adding structural arrangement and volume to species â area relationships across forest macrosystems |
Q59175697 | Do cryptic species matter in macroecology? Sequencing European groundwater crustaceans yields smaller ranges but does not challenge biodiversity determinants |
Q125824546 | Do ecological differences between taxonomic groups influence the relationship between speciesâ distributions and climate? A global metaâanalysis using species distribution models |
Q128006533 | Do genetic structure and landscape heterogeneity impact color morph frequency in a polymorphic salamander? |
Q60540305 | Do joint species distribution models reliably detect interspecific interactions from co-occurrence data in homogenous environments? |
Q120170079 | Do marine planktonic ciliates follow Bergmann's rule? |
Q110762520 | Do metacommunity mass effects predict changes in species incidence and abundance? |
Q60339033 | Do stream fish track climate change? Assessing distribution shifts in recent decades |
Q57062678 | Do they? How do they? WHY do they differ? On finding reasons for differing performances of species distribution models |
Q29012710 | Does a top predator reduce the predatory impact of an invasive mesopredator on an endangered rodent? |
Q58646583 | Does accounting for imperfect detection improve species distribution models? |
Q110762414 | Does environmental heterogeneity affect species co-occurrence in ecological guilds across stream macroinvertebrate metacommunities? |
Q125808708 | Does landscape structure affect resource tracking by avian frugivores in a fragmented Afrotropical forest? |
Q60130403 | Does multi-level environmental filtering determine the functional and phylogenetic composition of wild bee species assemblages? |
Q35114164 | Does probability of occurrence relate to population dynamics? |
Q60510153 | Does removal of an alien predator from small islands in the Baltic Sea induce a trophic cascade? |
Q57267181 | Does seed retention potential affect the distribution of plant species in highly fragmented calcareous grasslands? |
Q58827628 | Does seed retention potential affect the distribution of plant species in highly fragmented calcareous grasslands? |
Q57014917 | Does species diversity really drive speciation? |
Q57262041 | Does species richness drive speciation? A reassessment with the Hawaiian biota |
Q61465485 | Does the interpolation accuracy of species distribution models come at the expense of transferability? |
Q126122176 | Does wolf presence reduce moose browsing intensity in young forest plantations? |
Q112801062 | Drivers and interrelationships among multiple dimensions of rarity for freshwater fishes |
Q112800958 | Drivers of change in the realised climatic niche of terrestrial mammals |
Q60339031 | Drivers of freshwater fish colonisations and extirpations under climate change |
Q124527050 | Drivers of global variation in land ownership |
Q125939210 | Drivers of the spatial scale that best predict primate responses to landscape structure |
Q60400371 | Drought intensification drives turnover of structure and function in stream invertebrate communities |
Q126576567 | Drying determines the temporal dynamics of stream invertebrate structural and functional beta diversity |
Q104205924 | Dynamic and temporal structure of the troglobitic beetle Speonomus hydrophilus (Coleoptera: Bathyscimae) |
Q57030611 | Dynamic distribution modelling: predicting the present from the past |
Q60366513 | Dynamic populations in a dynamic landscape: the metapopulation structure of the marsh fritillary butterfly |
Q57193855 | Dynamic refugia and species persistence: tracking spatial shifts in habitat through time |
Q60476927 | Dynamic species co-occurrence networks require dynamic biodiversity surrogates |
Q54540524 | Dynamics of an introduced population of mouflonOvis arieson the sub-Antarctic archipelago of Kerguelen |
Q60310627 | Dynamics of haplogroup frequencies and survival rates in a contact zone of two mtDNA lineages of the lizard Lacerta vivipara |
Q122982960 | Dynamics of long-leaved sundew Drosera intermedia populations at two extremes of a hydrological gradient |
Q57013266 | Dynamics of mycorrhizae during development of riparian forests along an unregulated river |
Q120356169 | Dynamics or constancy inSphagnumdominated mire ecosystems? A 40-year study |
Q60442583 | E-Clic - easy climate data converter |
Q56754942 | ENM Components: a new set of web service-based workflow components for ecological niche modelling |
Q57003053 | ENMTools: a toolbox for comparative studies of environmental niche models |
Q112801068 | ENVIREM: an expanded set of bioclimatic and topographic variables increases flexibility and improves performance of ecological niche modeling |
Q59417299 | ENiRG: R-GRASS interface for efficiently characterizing the ecological niche of species and predicting habitat suitability |
Q109936123 | Early plant succession in two abandoned cut-over peatland areas |
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Q112800966 | Geographic patterns and environmental correlates of phylogenetic relatedness and diversity for freshwater fish assemblages in North America |
Q112800969 | Geographic patterns and environmental correlates of taxonomic and phylogenetic beta diversity for largeâscale angiosperm assemblages in China |
Q56554482 | Geographic profiling as a novel spatial tool for targeting the control of invasive species |
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Q125726817 | Geographic shifts in the effects of habitat size on trophic structure and decomposition |
Q57011460 | Geographic variability of ecological niches of plant species: are competition and stress relevant? |
Q57019576 | Geographic variation in fruit colour is associated with contrasting seed disperser assemblages in a south-Andean mistletoe |
Q58041040 | Geographic variation in resource use by specialist versus generalist butterflyfishes |
Q112798844 | Geographic variation in seed removal of a myrmecochorous herb: influence of variation in functional guild and species composition of the disperser assemblage through spatial and temporal scales |
Q57044564 | Geographic variation in the ecological effects of extinction of Australia's Pleistocene megafauna |
Q112801040 | Geographic variation of body size in New World anurans: energy and water in a balance |
Q112796932 | Geographical and ecological patterns of range size in North American trees |
Q124958824 | Geographical differences in habitat relationships of cetaceans across an ocean basin |
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Q60581486 | Geographical patterns in the beta diversity of China's woody plants: the influence of space, environment and range size |
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Q60581485 | Geography, environment, and spatial turnover of species in China's grasslands |
Q57068404 | Geography, topography, and history affect realized-to-potential tree species richness patterns in Europe |
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Q57269858 | Geomorphological disturbance is necessary for predicting fine-scale species distributions |
Q110704744 | Germination characteristics of some plant species from calcareous fens in southern Germany and their implications for the seed bank |
Q58644530 | Germination ecology of the polycarpic grassland perennials Primula veris and Trollius europaeus |
Q111492930 | Germination response to salt in Festuca rubra in a population from a salt marsh |
Q57269563 | Global gradients of avian longevity support the classic evolutionary theory of ageing |
Q120068868 | Global invasion history of the Mediterranean recluse spider: a concordance with human expansion |
Q60234467 | Global patterns and predictors of tropical reef fish species richness |
Q59312931 | Global patterns in the effects of predator declines on sea urchins |
Q127659034 | Global patterns of body size evolution are driven by precipitation in legless amphibians |
Q57233992 | Global patterns of environmental synchrony and the Moran effect |
Q57006568 | Global patterns of terrestrial assemblage turnover within and among land uses |
Q111264030 | Global patterns of the double mutualism phenomenon |
Q56429713 | Global phylogeography of the avian malaria pathogen Plasmodium relictum based on MSP1 allelic diversity |
Q56334590 | Global test of Eltonian niche conservatism of nonnative freshwater fish species between their native and introduced ranges |
Q112801002 | Global warming will affect the maximum potential abundance of boreal plant species |
Q112601987 | Globally consistent climate sensitivity of natural disturbances across boreal and temperate forest ecosystems |
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Q115527989 | Goshawk predation during winter, spring and summer in a boreal forest area of central Sweden |
Q108759877 | Graph theory illustrates spatial and temporal features that structure elephant rest locations and reflect risk perception |
Q114873628 | Grasshopper populations across 2000 m of altitude: is there life history adaptation? |
Q56480101 | Grassland connectivity by motor vehicles and grazing livestock |
Q58317936 | Greater consumption of protein-poor anthropogenic food by urban relative to rural coyotes increases diet breadth and potential for human-wildlife conflict |
Q114081983 | Green infrastructure can promote plant functional connectivity in a grassland species around fragmented semiânatural grasslands in NWâEurope |
Q57262131 | Grid-induced biases in connectivity metric implementations that use regular grids |
Q58389884 | Grizzly bear movements relative to roads: application of step selection functions |
Q125691983 | Groundâdwelling spiders (Arachnida, Araneae) in fragmented old forests and surrounding managed forests in southern Finland |
Q123250512 | Growth and body size in populations of mink frogs Rana septentrionalis from two latitudes |
Q121438395 | Growth and body size in populations of mink frogs Rana septentrionalis from two latitudes |
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Q109837717 | Growth of reindeer lichens and effects of reindeer grazing on ground cover vegetation in a Scots pine forest and a subarctic heathland in Finnish Lapland |
Q120016285 | Growth pattern and distribution of biomass of Calluna vulgaris on an ombrotrophic peat bog |
Q122599458 | Growth, maturation and survival of frogs Rana temporaria L. |
Q60537667 | Habitat area affects arthropod communities directly and indirectly through top predators |
Q112798851 | Habitat area affects arthropod communities directly and indirectly through top predators |
Q111376366 | Habitat associations of carabid beetles in fields and forests on the Aland Islands, SW Finland |
Q112784396 | Habitat associations of ducks during different phases of the breeding season |
Q125867285 | Habitat characteristics of Capercaillie Tetrao urogallus display grounds in southeastern Norway |
Q125703796 | Habitat distribution and conservation of land bird populations in northern Norway |
Q58045768 | Habitat disturbance selects against both small and large species across varying climates |
Q113181758 | Habitat diversity associated to island size and environmental filtering control the species richness of rockâsavanna plants in neotropical inselbergs |
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Q110789464 | Habitat fragmentation, not habitat loss, drives the prevalence of blood parasites in a Caribbean passerine |
Q56752636 | Habitat models and their transfer for single and multi species groups: a case study of carabids in an alluvial forest |
Q56752648 | Habitat models and their transfer for single and multi species groups: a case study of carabids in an alluvial forest |
Q111376359 | Habitat predictability and the occurrence of wood beetles in old-growth beech forests |
Q57649093 | Habitat preference and habitat exploration in two species of satyrine butterflies |
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Q124926744 | Habitat selection and group formation pattern of fallow deer Dama dama in a submediterranean environment |
Q57253819 | Habitat selection as a mechanism of resource partitioning in two cryptic bat speciesPipistrellus pipistrellusandPipistrellus pygmaeus |
Q58478866 | Habitat selection by a large herbivore at multiple spatial and temporal scales is primarily governed by food resources |
Q114625054 | Habitat selection, reproduction and survival of two small carabid species on arable land: a comparison between Trechus secalis and Bembidion lampros |
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Q58325634 | Habitat specifity, endemism and the neotropical distribution of Amazonian white-water floodplain trees |
Q60534908 | Habitat structural complexity metrics improve predictions of fish abundance and distribution |
Q126920276 | Habitat suitability models reveal the spatial signal of environmental DNA in riverine networks |
Q122739873 | Habitat use of small mustelids in north Fennoscandian tundra: a test of the hypothesis of patchy exploitation ecosystems |
Q115527971 | Habitat variability in the effects of predation and microclimate on mycophagous fly communities |
Q112798843 | Habitat, topographical, and geographical components structuring shrubsteppe bird communities |
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Q113794789 | Habitats, life histories, migration and dispersal by flight of two water-beetles Helophorus brevipalpis and H. strigifrons (Hydrophilidae) |
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Q114824047 | Herbarium specimens provide reliable estimates of phenological responses to climate at unparalleled taxonomic and spatiotemporal scales |
Q59732279 | Herbivore damage increases avian and ant predation of caterpillars on trees along a complete elevational forest gradient in Papua New Guinea |
Q57016506 | Heuristic and optimal solutions for set-covering problems in conservation biology |
Q112796918 | Hierarchical effects of environmental filters on the functional structure of plant communities: a case study in the French Alps |
Q125032432 | Hierarchical habitat selection by woodland caribou: its relationship to limiting factors |
Q112796930 | High connectivity among habitats precludes the relationship between dispersal and range size in tropical reef fishes |
Q114864534 | High elevation Plantago lanceolata plants are less resistant to herbivory than their low elevation conspecifics: is it just temperature? |
Q57001828 | High parasite infection level in non-native invasive species: it is just a matter of time |
Q59261446 | High specialization and limited structural change in plant-herbivore networks along a successional chronosequence in tropical montane forest |
Q56157123 | High summer temperature explains bill size variation in salt marsh sparrows |
Q129524978 | Highlighting declines of coldâdemanding plant species in lowlands under climate warming |
Q60234442 | Historical and contemporary determinants of global phylogenetic structure in tropical reef fish faunas |
Q56417800 | Historical climate-change influences modularity and nestedness of pollination networks |
Q123900946 | Historical data reveal contrasting habitat amount relationships with plant biodiversity |
Q56451144 | Historical data reveal power-law dispersal patterns of invasive aquatic species |
Q114146144 | Historical demography and climate driven distributional changes in a widespread Neotropical freshwater species with high economic importance |
Q58317483 | Historical distribution and regional dynamics of twoBrassicaspecies |
Q60141437 | Historical dynamics ofBatrachochytrium dendrobatidisin Amazonia |
Q110625762 | Historical legacies and ecological determinants of grass naturalizations worldwide |
Q123308363 | Home range and habitat use of wolverines Gulo gulo in Yukon, Canada |
Q53938971 | Home range size, habitat utilisation and movement patterns of suburban and farm cats Felis catus |
Q113042703 | Home range, activity and sociality of a top predator, the dingo: a test of the Resource Dispersion Hypothesis |
Q121364921 | Home ranges in moving habitats: polar bears and sea ice |
Q115527965 | Horizontal distribution of pelagic zooplankton in relation to predation gradients |
Q57261241 | Host community similarity and geography shape the diversity and distribution of haemosporidian parasites in Amazonian birds |
Q57269564 | Host diversity drives parasite diversity: meta-analytical insights into patterns and causal mechanisms |
Q110762529 | Host patch traits have scaleâdependent effects on diversity in a stickleback parasite metacommunity |
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Q104206943 | Host population density and body mass as determinants of species richness in parasite communities: comparative analyses of directly transmitted nematodes of mammals |
Q112800953 | Host specificity and species colouration mediate the regional decline of nocturnal moths in central European forests |
Q60537462 | Host-use patterns of saproxylic phloeophagous and xylophagous Coleoptera adults and larvae along the decay gradient in standing dead black spruce and aspen |
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Q60525566 | How do species interactions affect species distribution models? |
Q125290431 | How environmental drivers of spatial synchrony interact |
Q125798396 | How far is enough? Prediction of the scale of effect for wild bees |
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Q124334136 | How pondscapes function: connectivity matters for biodiversity even across small spatial scales in aquatic metacommunities |
Q59887789 | How to allow SAR collapse across local and continental scales: a resolution of the controversy between Storch et al. (2012) and Lazarina et al. (2013) |
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Q119576765 | How to survive a glaciation: the challenge of estimating biologically realistic potential distributions under freezing conditions |
Q112801107 | How universal are reserve design rules? A test using butterflies and their life history traits |
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Q57183578 | How well is current plant trait composition predicted by modern and historical forest spatial configuration? |
Q114081984 | Huge spring migrations of insects from the Middle East to Europe: quantifying the migratory assemblage and ecosystem services |
Q127556596 | Human overexploitation and extinction risk correlates of Chinese snakes |
Q59152268 | Humans and elephants as treefall drivers in African savannas |
Q112800998 | Humanâdominated land uses favour species affiliated with more extreme climates, especially in the tropics |
Q114146132 | Humanâinduced reduction in mammalian movements impacts seed dispersal in the tropics |
Q111172526 | Humanâmediated dispersal redefines mangrove biogeography in the Anthropocene |
Q113798989 | Humanâmediated trophic mismatch between fire, plants and herbivores |
Q73172241 | Humboldt Core - toward a standardized capture of biological inventories for biodiversity monitoring, modeling and assessment |
Q113345909 | Humpâshaped relationship between aggregation tendency and body size within fish populations |
Q111172402 | Hypervolume concepts in niche- and trait-based ecology |
Q109637910 | IUCN Red List protects avian genetic diversity |
Q59987780 | Identification of landscape units from an insect perspective |
Q57002845 | Identification of subpopulations from connectivity matrices |
Q114081989 | Identifying barriers to gene flow and hierarchical conservation units from seascape genomics: a modelling framework applied to a marine predator |
Q60472194 | Identifying in situ climate refugia for plant species |
Q112801132 | Identifying plant traits associated with topographic contrasts in a rugged and diverse region (Klamath-Siskiyou Mts, OR, USA) |
Q58195617 | Identifying recorder-induced geographic bias in an Iberian butterfly database |
Q57257764 | Identifying spatial relationships at multiple scales: principal coordinates of neighbour matrices (PCNM) and geostatistical approaches |
Q58253073 | Idiosyncratic responses of Pacific salmon species to land cover, fragmentation, and scale |
Q57257760 | Illustrations and guidelines for selecting statistical methods for quantifying spatial pattern in ecological data |
Q122924624 | Impact of cervid browsing and grazing on the terrestrial gastropod fauna in the boreal forests of Fennoscandia |
Q112796961 | Impact of climate change factors on the clonal sedge Carex bigelown: implications for population growth and vegetative spread |
Q56740746 | Impact of host plant quality on geometrid moth expansion on environmental and local population scales |
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Q113798490 | Impact of simulated moose densities on abundance and richness of vegetation, herbivorous and predatory arthropods along a productivity gradient |
Q56814611 | Impact of warming and timing of snow melt on soil microarthropod assemblages associated with Dryas-dominated plant communities on Svalbard |
Q112800951 | Impacts of beekeeping on wild bee diversity and pollination networks in the Aegean Archipelago |
Q57616118 | Impacts of climate change on national biodiversity population trends |
Q126119377 | Imperfect detection distorts depthârelated trends in marine macrofaunal species richness |
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Q60565503 | Implications of Liebig's law of the minimum for the use of ecological indicators based on abundance |
Q56096188 | Implications of long-distance movements of frugivorous rain forest hornbills |
Q124980380 | Importance of antecedent environmental conditions in modeling species distributions |
Q120686473 | Importance of biotic niches versus drift in a plantâinhabiting arthropod community depends on rarity and trophic group |
Q57195055 | Importance of estimating matrix quality for modeling species distribution in complex tropical landscapes: a test with Atlantic forest small mammals |
Q121743241 | Importance of spatioâtemporal connectivity to maintain species experiencing range shifts |
Q122924906 | Importance of spruce swamp-forests for epiphyte diversity and flora on Picea abies in southern and middle boreal Finland |
Q57268858 | Important marine habitat off east Antarctica revealed by two decades of multi-species predator tracking |
Q56886429 | Improved species-occurrence predictions in data-poor regions: using large-scale data and bias correction with down-weighted Poisson regression and Maxent |
Q113798987 | Improving landscapeâscale productivity estimates by integrating traitâbased models and remotelyâsensed foliarâtrait and canopyâstructural data |
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Q114624975 | Improving species occupancy estimation when sampling violates the closure assumption |
Q57007781 | Incorporating biotic factors in species distribution modeling: are interactions with soil microbes important? |
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Q112801007 | Incorporating intraspecific variation into species distribution models improves distribution predictions, but cannot predict species traits for a wideâspread plant species |
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Q111172411 | Incorporating physiology into species distribution models moderates the projected impact of warming on selected Mediterranean marine species |
Q129231127 | Incorporating the geometry of dispersal and migration to understand spatial patterns of species distributions |
Q56879807 | Increase of island endemism with altitude - speciation processes on oceanic islands |
Q114144828 | Increasing insect abundance by killing deciduous trees: a method of improving the food situation for endangered woodpeckers |
Q57520004 | Increasing rate of species discovery in sharks coincides with sharp population declines: implications for biodiversity |
Q106890062 | Increasing synergistic effects of habitat destruction and hunting on mammals over three decades in the Gran Chaco |
Q60410243 | Increasing temperature may compensate for lower amounts of dead wood in driving richness of saproxylic beetles |
Q56158260 | Incubation rhythm in the great snipe Gallinago media |
Q57636063 | Indirect seed dispersal by the feral cats Felis catus in island ecosystems (Canary Islands) |
Q128426725 | Individual and temporal variation in movement patterns of wild alpine reindeer and implications for disease management |
Q120686468 | Individual contribution to niche expansion in amphibians: a test of the niche variation hypothesis |
Q57122497 | Individual species-area relationships and spatial patterns of species diversity in a Great Basin, semi-arid shrubland |
Q123198721 | Individualistic response to past climate changes: niche differentiation promotes diverging Quaternary range dynamics in the subspecies of Testudo graeca |
Q57021243 | Individualistic vs community modelling of species distributions under climate change |
Q112796966 | Induced defence reaction in Scots pine following stem attacks by Tomicus piniperda |
Q30876899 | Inference from presence-only data; the ongoing controversy |
Q112801026 | Inference of biogeographic history by formally integrating distinct lines of evidence: genetic, environmental niche and fossil |
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Q60394511 | Inferring behavioural mechanisms in habitat selection studies getting the null-hypothesis right for functional and familiarity responses |
Q60525559 | Inferring the similarity of species distributions using Speciesâ Distribution Models |
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Q57267290 | Influence of environmental and spatial variables on regional distribution of forest plant species in a fragmented and changing landscape |
Q57267316 | Influence of land use history on seed banks in European temperate forest ecosystems: a review |
Q60578852 | Influence of the food plant, Urtica dioica, on larval development, feeding efficiences, and voltinism of a specialist insect, Inachis io |
Q125938659 | Influence of the geography of speciation on current patterns of coral reef fish biodiversity across the IndoâPacific |
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Q60572531 | Influence of weather conditions on pallid swift Apus pallidus breeding success |
Q113033788 | Influences on the density and dispersion of bumble bee nests (Hymenoptera: Apidae) |
Q114081988 | Informed dispersal based on prospecting impacts the rate and shape of range expansions |
Q113794770 | Insect herbivory on water mint: you can't get there from here? |
Q112800975 | Insect occurrence in agricultural landâuses depends on realized niche and geographic range properties |
Q128954112 | Insect wing loss is tightly linked to the treeline: evidence from a diverse stonefly assemblage |
Q126167124 | Insular patterns of calicioid lichens in a boreal oldâgrowth forestâwetland mosaic |
Q127926797 | Integrated modeling predicts shifts in waterbird population dynamics under climate change |
Q127010589 | Integrated population model reveals that kestrels breeding in nest boxes operate as a source population |
Q126303795 | Integrated species distribution models fitted in INLA are sensitive to mesh parameterisation |
Q125476644 | Integrating data from different taxonomic resolutions to better estimate community alpha diversity |
Q57021518 | Integrating ecophysiological models into species distribution projections of European reptile range shifts in response to climate change |
Q59404608 | Integrating highly diverse invertebrates into broad-scale analyses of cross-taxon congruence across the Palaearctic |
Q60254861 | Integrating large-scale geographic patterns in flight morphology, flight characteristics and sexual selection in a range-expanding damselfly |
Q113798985 | Integrating physiology into correlative models can alter projections of habitat suitability under climate change for a threatened amphibian |
Q56768712 | Integrating physiology, population dynamics and climate to make multi-scale predictions for the spread of an invasive insect: the Argentine ant at Haleakala National Park, Hawaii |
Q57257761 | Integrating the statistical analysis of spatial data in ecology |
Q115405646 | Integrating trait and phylogenetic distances to assess scale-dependent community assembly processes |
Q61886993 | Integrating transport pressure data and species distribution models to estimate invasion risk for alien stowaways |
Q125567251 | Integration of presenceâonly data from several sources: a case study on dolphins' spatial distribution |
Q60481622 | Inter-individual variation promotes ecological success of populations and species: evidence from experimental and comparative studies |
Q56331053 | Inter-regional hybrids of native and invasive Centaurea solstitialis display intermediate competitive ability |
Q110775513 | Interactions among species with contrasting dispersal modes explain distributions for epiphytic lichens |
Q121613481 | Interactions between two rust fungi and their host plantAnemone nemorosa |
Q120016253 | Interactive effects of distance and matrix on the movements of a peatland dragonfly |
Q126046978 | Interactive effects of keystone rodents on the structure of desert grassland arthropod communities |
Q58108320 | Interannual changes in folivory and bird insectivory along a natural productivity gradient in northern Patagonian forests |
Q57139988 | Interdependency of plants and animals in controlling the sodium balance of ecosystems and the impacts of global defaunation |
Q60484221 | Internal structure and patterns of contraction in the geographic range of the Iberian lynx |
Q122980999 | Interspecific and intraspecific variations in egg hatching for British populations of Taeniopteryx nebulosa and Brachyptera risi (Plecoptera: Taeniopterygidae) |
Q120686460 | Interspecific territoriality has facilitated recent increases in the breeding habitat overlap of North American passerines |
Q114146137 | Intertwined effects of defaunation, increased tree mortality and density compensation on seed dispersal |
Q124810811 | Interâ and intraspecific variation in the resistance of winterâdormant birch (Betula spp.) against browsing by the mountain hare |
Q56884454 | Intraguild predation of lynxes on foxes: evidence of interference competition? |
Q112796963 | Intraseasonal variation in pollination intensity and seed set in an alpine population of Ranunculus acris in southwestern Norway |
Q60534096 | Intraspecific facilitation: a missing process along increasing stress gradients - insights from simulated shrub populations |
Q57124103 | Intraspecific facilitation: a missing process along increasing stress gradients ? insights from simulated shrub populations |
Q126177781 | Intraspecific variation in nitrogen status and photosynthetic capacity within mountain birch populations |
Q60568944 | Introduced megafauna are rewilding the Anthropocene |
Q60147820 | Introducing the biogeographic species pool |
Q57043689 | Invariant antagonistic network structure despite high spatial and temporal turnover of interactions |
Q56594952 | Invasibility: the local mechanism driving community assembly and species diversity |
Q56774940 | Invasion dynamics of an introduced squirrel in Argentina |
Q60507619 | Invasion of the Hawaiian Islands by a parasite infecting imperiled stream fishes |
Q126920246 | Invasion risk of the currently cultivated alien flora in southern Africa is predicted to decline under climate change |
Q55328252 | Invasion success and threat status: two sides of a different coin? |
Q110625863 | Invasion success and tolerance to urbanization in birds |
Q55842119 | Invasions |
Q120170080 | Invasionâmediated mutualism disruption is evident across heterogeneous environmental conditions and varying invasion intensities |
Q57034279 | Invasive and nativeRhododendron ponticumpopulations: is there evidence for genotypic differences in germination and growth? |
Q56767583 | Invasive birds in a novel landscape: habitat associations and effects on established species |
Q56461489 | Invasive plants in conservation linkages: a conceptual model that addresses an underappreciated conservation issue |
Q111147495 | Invasive ring-necked parakeets Psittacula krameri in Belgium: habitat selection and impact on native birds |
Q124879684 | Invasive ring-necked parakeets Psittacula krameri in Belgium: habitat selection and impact on native birds |
Q112796927 | Investigating niche and lineage diversification in widely distributed taxa: phylogeography and ecological niche modeling of thePeromyscus maniculatusspecies group |
Q56785407 | Investigating spatial structure in specific tree species in ancient semi-natural woodland using remote sensing and marked point pattern analysis |
Q60400927 | Investigating spatial structure in specific tree species in ancient semi-natural woodland using remote sensing and marked point pattern analysis |
Q60469551 | Investigating uncertainties in zooplankton composition shifts under climate change scenarios in the Mediterranean Sea |
Q62556903 | Is farther seed dispersal better? Spatial patterns of offspring mortality in three rainforest tree species with different dispersal abilities |
Q56376463 | Is phylogeography helpful for invasive species risk assessment? The case study of the bark beetle genus Dendroctonus |
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Q112796455 | Is the population turnover of patchy-distributed annuals determined by dormancy dynamics or dispersal processes? |
Q59156189 | Is there a correlation between abundance and environmental suitability derived from ecological niche modelling? A meta-analysis |
Q113856790 | Is there a higher risk for herbivore outbreaks after cold mast years? An analysis of two plant/herbivore series from southern Norway |
Q113794751 | Is there a higher risk for herbivore outhreaks after cold mast years? An analysis of two plant/herbivore series from southern Norway |
Q57234493 | Is there a latitudinal gradient in seed production? |
Q113345348 | Island biogeography of North European parthenogenetic Lumbricidae: I. Clone pool affinities and morphometric differentiation of Aland populations |
Q112800987 | Island properties dominate species traits in determining plant colonizations in an archipelago system |
Q60297443 | Island, archipelago and taxon effects: mixed models as a means of dealing with the imperfect design of nature's experiments |
Q59786916 | Island-wide aridity did not trigger recent megafaunal extinctions in Madagascar |
Q61702331 | Islands in the ice: colonisation routes for rock ptarmigan to the Svalbard archipelago |
Q112796931 | Islands in the sky or squeezed at the top? Ecological causes of elevational range limits in montane salamanders |
Q57195005 | Isolation determines patterns of species presence in highly fragmented landscapes |
Q60234428 | Isolation drives taxonomic and functional nestedness in tropical reef fish faunas |
Q56933740 | Isolation predicts compositional change after discrete disturbances in a global meta-study |
Q60532427 | Isolation-driven functional assembly of plant communities on islands |
Q58192279 | Isotopic analysis of the sources of organic carbon for zooplankton in shallow subarctic and arctic waters |
Q58192283 | Isotopic analysis of the sources of organic carbon for zooplankton in shallow subarctic and arctic waters |
Q114081999 | Joint analysis of species and genetic variation to quantify the role of dispersal and environmental constraints in community turnover |
Q114551981 | Jumping into the grids: mapping biodiversity hotspots in groundwater habitat types across Europe |
Q59588240 | KISSMig - a simple model for R to account for limited migration in analyses of species distributions |
Q29395296 | Keystone rodent interactions: prairie dogs and kangaroo rats structure the biotic composition of a desertified grassland |
Q54887947 | Knowledge-based models for predicting species occurrence in arable conditions |
Q56453074 | LANDIS PRO: a landscape model that predicts forest composition and structure changes at regional scales |
Q111934420 | LORACS: JAVA software for modeling landscape connectivity and matrix permeability |
Q56767580 | Land-use and isolation interact to affect wetland plant assemblages |
Q57201151 | Land-use effects on the functional distinctness of arthropod communities |
Q57217166 | Land-use history, historical connectivity, and land management interact to determine longleaf pine woodland understory richness and composition |
Q125388104 | Landscape and area effects on beetle assemblages in Ontario |
Q109351294 | Landscape characteristics associated with the occurrence of the flying squirrel Pteromys volans in old-growth forests of northern Finland |
Q60557387 | Landscape composition, not connectivity, determines metacommunity structure across multiple scales |
Q57134877 | Landscape context affects the relationship between local and landscape species richness of butterflies in semi-natural habitats |
Q56450368 | Landscape diversity slows the spread of an invasive forest pest species |
Q58644245 | Landscape effects on butterfly assemblages in an agricultural region |
Q115212718 | Landscape issues in plant ecology |
Q57025836 | Landscape matrix modifies richness of plants and insects in grassland fragments |
Q56672780 | Landscape partitioning and spatial inferences of competition between black and grizzly bears |
Q125381151 | Landscape scale variation in the hydrologic niche of California coast redwood |
Q57247621 | Landscape structure and genetic architecture jointly impact rates of niche evolution |
Q60255072 | Landscape structure, dispersal and the evolution of antagonistic plant-herbivore interactions |
Q127011137 | Landscape transformation alters functional diversity in coastal seascapes |
Q56417828 | Landscape, cropping and field boundary influences on bird abundance |
Q57038651 | Landscape- and small-scale determinants of grassland species diversity: direct and indirect influences |
Q127172951 | Landscapeâscale habitat response of African elephants shows strong selection for foraging opportunities in a human dominated ecosystem |
Q60569758 | Large forests enhance songbird nesting success in agricultural- dominated landscapes of the Midwestern US |
Q112796962 | Large plant size counteracts early seed predation during the extended flowering season of a Silene uniflora (Caryophyllaceae) population |
Q57010849 | Large reorganizations in butterfly communities during an extreme weather event |
Q58427874 | Large scale geographic clines of parasite damage toPopulus tremulaL |
Q115533040 | Large-scale movement behavior in a reintroduced predator population |
Q60128315 | Large-scale oceanographic fluctuations drive Antarctic petrel survival and reproduction |
Q54982352 | Large-scale patterns in genetic variation, gene flow and differentiation in five species of European Coenagrionid damselfly provide mixed support for the central-marginal hypothesis |
Q60317152 | Large-scale spatial ecology of dung beetles |
Q60317243 | Large-scale spatial ecology of dung beetles |
Q60486550 | Large-scale spatial variation in palm fruit abundance across a tropical moist forest estimated from high-resolution aerial photographs |
Q126181134 | Largeâscale patterns of summer and winter bird distribution in relation to farmland type in England and Wales |
Q60547414 | Larval dispersal dampens population fluctuation and shapes the interspecific spatial distribution patterns of rocky intertidal gastropods |
Q60548092 | Larval dispersal of intertidal organisms and the influence of coastline geography |
Q56700095 | Larval survival in populations of the large copper butterfly Lycaena dispar batavus |
Q58488487 | Lasting effects of conditions at birth on moose body mass |
Q126201023 | Late Holocene deforestation of a tree line site: estimation of preâfire vegetation composition and black spruce cover using soil charcoal |
Q60179951 | Latitude-wide genetic patterns reveal historical effects and contrasting patterns of turnover and nestedness at the range peripheries of a tropical marine fish |
Q57599224 | Latitudinal and altitudinal patterns of plant community diversity on mountain summits across the tropical Andes |
Q109400480 | Latitudinal clines in the timing and temperatureâsensitivity of photoperiodic reproductive diapause inDrosophila montana |
Q118391153 | Latitudinal diversity patterns in estuarine tidal flats: indications of a global cline |
Q57032581 | Latitudinal gradient of nestedness and its potential drivers in stream detritivores |
Q114624964 | Latitudinal gradients in North American avian species richness, turnover rates and extinction probabilities |
Q57950491 | Latitudinal gradients in diversity: real patterns and random models |
Q60488608 | Latitudinal gradients in diversity: real patterns and random models |
Q112796949 | Latitudinal gradients in species diversity and Rapoport's rule revisited: a review of recent work and what can parasites teach us about the causes of the gradients? |
Q57006683 | Latitudinal gradients in taxonomic overdescription rate affect macroecological inferences using species list data |
Q128431214 | Latitudinal gradients of parasite richness: a review and new insights from helminths of cricetid rodents |
Q108040213 | Latitudinal patterns in intertidal ecosystem structure in West Greenland suggest resilience to climate change |
Q56171487 | Latitudinal trends in body size among over-wintering leaf warblers (genusPhylloscopus) |
Q60292476 | Latitudinal variation in plant chemical defences drives latitudinal patterns of leaf herbivory |
Q60581502 | Leaf nitrogen and phosphorus concentrations of woody plants differ in responses to climate, soil and plant growth form |
Q64004685 | Lean-season primary productivity and heat dissipation as key drivers of geographic body-size variation in a widespread marsupial |
Q64032117 | Learning from the past to prepare for the future: felids face continued threat from declining prey |
Q114146116 | Legacy effects of drought on tree growth responses to hurricanes |
Q127013052 | Liana abundance and diversity increase with rainfall seasonality along a precipitation gradient in Panama |
Q116809646 | Lichens on dead wood: species-substrate relationships in the epiphytic lichen floras of the Pacific Northwest and Fennoscandia |
Q115532210 | Life cycle period and activity of prey influence their susceptibility to predators |
Q125904386 | Life history diversity in terrestrial animals is associated with metabolic response to seasonally fluctuating resources |
Q113172354 | Life history traits and resource utilisation in an assemblage of north temperate Aphodius dung beetles (Coleoptera: Scarabaeidae) |
Q58042083 | Life history traits, but not body size, vary systematically along latitudinal gradients on three continents in the widespread yellow dung fly |
Q63613168 | Life history variation across a riverine landscape: intermediate levels of disturbance favor sexual reproduction in the ant-dispersed herbRanunculus ficaria |
Q57124259 | Life history variation in an annual plant under two opposing environmental constraints along an aridity gradient |
Q110068505 | Lifeâhistory dimensions indicate nonârandom assembly processes in tropical island tree communities |
Q60579200 | Likely responses of the Antarctic benthos to climate-related changes in physical disturbance during the 21st century, based primarily on evidence from the West Antarctic Peninsula region |
Q123990486 | Limited impact of microtopography on alpine plant distribution |
Q58380850 | Linkages between large-scale climate patterns and the dynamics of Arctic caribou populations |
Q112796938 | Linking bird, carabid beetle and butterfly life-history traits to habitat fragmentation in mosaic landscapes |
Q57251290 | Linking habitat use to range expansion rates in fragmented landscapes: a metapopulation approach |
Q112801047 | Linking species richness and size diversity in birds and fishes |
Q59048451 | Linking trait variation to the environment: critical issues with community-weighted mean correlation resolved by the fourth-corner approach |
Q61811234 | Living on predictability: modelling the density distribution of efficient foraging seabirds |
Q57409686 | Local and cross-seasonal associations of climate and land use with abundance of monarch butterflies Danaus plexippus |
Q56769800 | Local and landscape correlates of non-native species invasion in restored wetlands |
Q126177354 | Local and regional species richness in communities of surfaceâdwelling grassland Collembola: indication of species saturation |
Q57950488 | Local avian assemblages as random draws from regional pools |
Q114146149 | Local extinctions of obligate frugivores and patch size reduction disrupt the structure of seed dispersal networks |
Q109351272 | Local habitat patch pattern of the Siberian flying squirrel in a managed boreal forest landscape |
Q112801110 | Local human impacts decouple natural biophysical relationships on Pacific coral reefs |
Q59169277 | Local species assemblages are influenced more by past than current dissimilarities in photosynthetic activity |
Q57055912 | Locality or habitat? Exploring predictors of biodiversity in Amazonia |
Q57062384 | Logistic regression models for predicting occurrence of terrestrial molluscs in southern Sweden - importance of environmental data quality and model complexity |
Q115557294 | Long term effects of cormorant predation on fish communities and fishery in a freshwater lake |
Q58834797 | Long-distance dispersal of seeds in the fire-tolerant shrub Banksia attenuata |
Q56948371 | Long-distance dispersal syndromes matter: diaspore-trait effect on shaping plant distribution across the Canary Islands |
Q57589937 | Long-lived and heavier females give birth earlier in roe deer |
Q56782633 | Long-term consequences of the alteration of the seed dispersal process ofEuphorbia characiasdue to the Argentine ant invasion |
Q60545925 | Long-term demographic fluctuations of the spur-thighed tortoise Testudo graeca in SW Spain |
Q56747582 | Long-term persistence and spatial assortment of nonnative plant species in second-growth forests |
Q57950495 | Long-term satellite telemetry of the movements and habitat utilisation by green turtles in the Mediterranean |
Q60566990 | Long-term succession in a Danish temperate deciduous forest |
Q59361527 | Longitudinal gradients in the phylogenetic community structure of European Tenebrionidae (Coleoptera) do not coincide with the major routes of postglacial colonization |
Q60515423 | Longitudinal structure, density and production rates of a neotropical stream fish assemblage: the river Ubatiba in the Serra do Mar, southeast Brazil |
Q60515426 | Longitudinal structure, density and production rates of a neotropical stream fish assemblage: the river Ubatiba in the Serra do Mar, southeast Brazil |
Q112800919 | Longâterm changes in flowering synchrony reflect climatic changes across an elevational gradient |
Q120686464 | Longâterm coastal macrobenthic Community Trajectory Analysis reveals habitatâdependent stability patterns |
Q129600462 | Longâterm drought triggers severe declines in carabid beetles in a temperate forest |
Q126191158 | Longâterm microtine dynamics in north Fennoscandian tundra: the vole cycle and the lemming chaos |
Q60362671 | Looking at the unseen: combining animal bio-logging and stable isotopes to reveal a shift in the ecological niche of a deep diving predator |
Q57012380 | Loss of habitat and connectivity erodes species diversity, ecosystem functioning, and stability in metacommunity networks |
Q57191455 | Lotic dispersal of lentic macroinvertebrates |
Q73172236 | Low bird diversity in the Fynbos plant diversity hotspot: Quaternary legacies in the current distributions of passerine birds |
Q112796456 | Low dispersal ability and habitat specificity promote extinctions in rare but not in widespread species: the Orthoptera of Germany |
Q115527966 | Low ungulate biomass in west African savannas: primary production or missing megaherbivores or large predator species? |
Q60442480 | MODULAR: software for the autonomous computation of modularity in large network sets |
Q112800942 | Macroclimatic structuring of spatial phylogenetic turnover in liverworts |
Q56741782 | Macroecological and macroevolutionary patterns emerge in the universe of GNU/Linux operating systems |
Q56650663 | Macroecological drivers of alien conifer naturalizations worldwide |
Q60551333 | Macroecological drivers of zooplankton communities across the mountains of western North America |
Q101632318 | Macroecology and macroevolution of body size in Anolis lizards |
Q56434621 | Macroecology of global bryophyte invasions at different invasion stages |
Q112800979 | Mammal population densities at a global scale are higher in humanâmodified areas |
Q115557283 | Mammalian predator scent, vegetation cover and tree seedling predation by meadow voles |
Q56481228 | Management history determines gene flow in a prominent invader |
Q112279678 | Marrow fat content, sex and age of red deer killed by wolves in winter in the Carpathian Mountains |
Q120016256 | Mass balance and nitrogen accumulation in hummocks on a South Swedish bog during the late Holocene |
Q57233958 | Mast-producing trees and the geographical ecology of western scrub-jays |
Q57032751 | Measures, perceptions and scaling patterns of aggregated species distributions |
Q60442416 | Mechanisms of interaction between a leguminous shrub and its understorey in a semi-arid environment |
Q113794775 | Mechanisms regulating bird predation on a herbivorous Larva guild in boreal coniferous forests |
Q56038575 | Mechanisms underlying the interaction betweenPinus halepensisand the native late-successional shrubPistacia lentiscusin a semi-arid plantation |
Q123419584 | Mechanistic insights into the role of large carnivores for ecosystem structure and functioning |
Q56444108 | Mechanistic modelling of animal dispersal offers new insights into range expansion dynamics across fragmented landscapes |
Q60464158 | Mechanistic simulation models in macroecology and biogeography: state-of-art and prospects |
Q107474442 | Megafauna decline have reduced pathogen dispersal which may have increased emergent infectious diseases |
Q57067977 | Megafauna extinction, tree species range reduction, and carbon storage in Amazonian forests |
Q57067982 | Megafauna in the Earth system |
Q110623401 | Megafrugivores as fading shadows of the past: extant frugivores and the abiotic environment as the most important determinants of the distribution of palms in Madagascar |
Q108676964 | Megaherbivore impacts on ecosystem and Earth system functioning: the current state of the science |
Q125589760 | Mercury levels in feathers of eagleâowls Bubo bubo in a captive, a reintroduced and a native wild population in SW Sweden |
Q57012559 | Metacommunity diversity depends on connectivity and patch arrangement in heterogeneous habitat networks |
Q110762563 | Metacommunity resilience against simulated gradients of wildfire: disturbance intensity and species dispersal ability determine landscape recover capacity |
Q57123585 | Metacommunity, mainland-island system or island communities? Assessing the regional dynamics of plant communities in a fragmented landscape |
Q120016247 | Metapopulation dynamics of the bog fritillary butterfly: experimental changes in habitat quality induced negative density-dependent dispersal |
Q108872044 | Metapopulation shift and survival of woodland birds under climate change: will species be able to track? |
Q57267155 | Metapopulation viability of an endangered holoparasitic plant in a dynamic landscape |
Q117306766 | Metaâanalysis of Antarctic phylogeography reveals strong sampling bias and critical knowledge gaps |
Q58069900 | Method selection for species distribution modelling: are temporally or spatially independent evaluations necessary? |
Q110789463 | Methods and models for identifying thresholds of habitat loss |
Q56817176 | Methods to account for spatial autocorrelation in the analysis of species distributional data: a review |
Q57211292 | Microbial biogeography of permafrost thaw ponds across the changing northern landscape |
Q56925475 | Microclimate variability in alpine ecosystems as stepping stones for non-native plant establishment above their current elevational limit |
Q60447105 | Microclimatic buffering in forests of the future: the role of local water balance |
Q120016447 | Microcommunities of algae on a Sphagnum mat |
Q121711616 | Microcrustacean community structure and biomass in marsh and lake habitats of the Okefenokee Swamp: seasonal dynamics and responses to resource manipulations |
Q125926257 | Microfungi of a Danish Beech forest Microbiology of a Danish beech forest II |
Q114082003 | Microhabitat analyses support relationships between niche breadth and range size when spatial autocorrelation is strong |
Q114080275 | Microhabitats of stream invertebrates on two submersed macrophytes with contrasting leaf morphology |
Q120016258 | Microsite and regional variation in the potential decay rate of Sphagnum magellanicum in south Swedish raised bogs |
Q121832061 | Migration of hawksbill turtlesEretmochelys imbricatafrom Tortuguero, Costa Rica |
Q56991644 | Migration, invasion and decline: changes in recruitment and forest structure in a warming-linked shift of European beech forest in Catalonia (NE Spain) |
Q127887805 | Migratory shorebird adheres to Bergmann's Rule by responding to environmental conditions through the annual lifecycle |
Q56945873 | Migratory strategies of waterbirds shape the continental-scale dispersal of aquatic organisms |
Q126795040 | Millennialâscale change in the structure of a Caribbean reef ecosystem and the role of human and natural disturbance |
Q112800991 | Miniaturizing landscapes to understand species distributions |
Q60297038 | Minimum required number of specimen records to develop accurate species distribution models |
Q111926121 | ModEco: an integrated software package for ecological niche modeling |
Q56937385 | Model-based integration of observed and expert-based information for assessing the geographic and environmental distribution of freshwater species |
Q60314700 | Modeling bird species distribution change in fire prone Mediterranean landscapes: incorporating species dispersal and landscape dynamics |
Q107459959 | Modeling of species distributions with Maxent: new extensions and a comprehensive evaluation |
Q56389120 | Modeling spatial expansion of invasive alien species: relative contributions of environmental and anthropogenic factors to the spreading of the harlequin ladybird in France |
Q58709141 | Modeling the climatic drivers of spatial patterns in vegetation composition since the Last Glacial Maximum |
Q114627643 | Modelled midâtrophic pelagic prey fields improve understanding of marine predator foraging behaviour |
Q58192725 | Modelling habitat distributions for multiple species using phylogenetics |
Q125884325 | Modelling how people and nature are intertwined |
Q61465368 | Modelling spatial patterns in harbour porpoise satellite telemetry data using maximum entropy |
Q57198250 | Modelling species distributions in Britain: a hierarchical integration of climate and land-cover data |
Q56774004 | Modelling species distributions without using species distributions: the cane toad in Australia under current and future climates |
Q126510051 | Modelling species presenceâonly data with random forests |
Q60509696 | Modelling species responses to extreme weather provides new insights into constraints on range and likely climate change impacts for Australian mammals |
Q112801139 | Modelling surface fine fuel dynamics across climate gradients in eucalypt forests of south-eastern Australia |
Q56817114 | Modelling the impact of climate and land use change on the geographical distribution of leaf anatomy in a temperate flora |
Q57032392 | Modelling the impact ofHieraciumspp. on protected areas in Australia under future climates |
Q60572788 | Modelling the niche for a marine vertebrate: a case study incorporating behavioural plasticity, proximate threats and climate change |
Q60148175 | Modelling the species richness distribution for French Aphodiidae (Coleoptera, Scarabaeoidea) |
Q112796911 | Modularity along organism dispersal gradients challenges a prevailing view of abrupt transitions in animal landscape perception |
Q60404410 | Molecular substitution rate increases with latitude in butterflies: evidence for a trans-glacial latitudinal layering of populations? |
Q57014771 | Mollusk species diversity in the Southeastern Pacific: why are there more species towards the pole? |
Q111829936 | Monitoring habitat dynamics for rare and endangered species using satellite images and niche-based models |
Q57199161 | Monitoring temporal trends in spatially structured populations: how should sampling effort be allocated between space and time? |
Q60488023 | Moose and vole browsing patterns in experimentally assembled pure and mixed forest stands |
Q112800911 | More than what they eat: uncoupled biophysical constraints underlie geographic patterns of herbivory |
Q56817026 | Morphological trait matching shapes plant-frugivore networks across the Andes |
Q57248509 | Mortality and lamb body mass growth in free-ranging domestic sheep - environmental impacts including lethal and non-lethal impacts of predators |
Q112801039 | Moth body size increases with elevation along a complete tropical elevational gradient for two hyperdiverse clades |
Q110762522 | Mountain metacommunities: climate and spatial connectivity shape ant diversity in a complex landscape |
Q56334584 | Mountain roads shift native and non-native plant species' ranges |
Q57123628 | Movement upscaled - the importance of individual foraging movement for community response to habitat loss |
Q57030138 | Multi-causality and spatial non-stationarity in the determinants of groundwater crustacean diversity in Europe |
Q29032116 | Multi-generational long-distance migration of insects: studying the painted lady butterfly in the Western Palaearctic |
Q56936842 | Multi-scale patterns of forest structure and species composition in relation to climate in northeast China |
Q60359783 | Multi-scale spatial patterns of three seagrass species with different growth dynamics |
Q58856678 | Multi-trophic guilds respond differently to changing elevation in a subtropical forest |
Q112801079 | Multicontinental community phylogenetics of avian mixed-species flocks reveal the role of the stability of associations and of kleptoparasitism |
Q60315893 | Multiple environmental stressors increase the realised niche breadth of a forest-dwelling fish |
Q56837875 | Multiple habitat associations: the role of offsite habitat in determining onsite avian density and species richness |
Q122945989 | Multiple interacting ecosystem drivers: toward an encompassing hypothesis of oak forest dynamics across eastern North America |
Q57205101 | Multiple site dissimilarity quantifies compositional heterogeneity among several sites, while average pairwise dissimilarity may be misleading |
Q112796935 | Multiple successional pathways of boreal forest stands in central Canada |
Q60445625 | Multispecies interactions across trophic levels at macroscales: retrospective and future directions |
Q125474484 | Multiâcolony tracking of two pelagic seabirds with contrasting flight capability illustrates how windscapes shape migratory movements at an oceanâbasin scale |
Q100252552 | Multiâspecies occupancy models: review, roadmap, and recommendations |
Q112603548 | Multiâtaxa colonisation along the foreland of a vanishing equatorial glacier |
Q101632319 | Museums and cradles of diversity are geographically coincident for narrowly distributed Neotropical snakes |
Q57190990 | Muskrat life history: a comparison of a northern and southern population |
Q56425051 | Mycorrhizal associations of an invasive tree are enhanced by both genetic and environmental mechanisms |
Q112801038 | Mycorrhizal symbiosis increases the benefits of plant facilitative interactions |
Q111492924 | N2(C2H2)-fixation in early stages of a primary succession on a reclaimed salt marsh |
Q64032137 | NCBIminer: sequences harvest from Genbank |
Q60400373 | NOS: a software suite to compute node overlap and segregation in ecological networks |
Q56094366 | Naive birds and noble savages - a review of man-caused prehistoric extinctions of island birds |
Q114929296 | Native and alien invasive plants: more of the same? |
Q111172475 | Native and invasive hosts play different roles in hostâparasite networks |
Q111425488 | Natural age and size of Pinus sylvestris and Picea abies on a mire in the inland part of northern Sweden |
Q57030172 | Natural fragmentation in river networks as a driver of speciation for freshwater fishes |
Q60147925 | Negative range size-abundance relationships in Indo-Pacific bird communities |
Q112796458 | Neighbor effects on germination, survival, and growth in two arctic tundra plant communities |
Q58387807 | Neighbourhood analyses of tree seed predation by introduced rodents in a New Zealand temperate rainforest |
Q60521994 | Neighbourhood analyses of tree seed predation by introduced rodents in a New Zealand temperate rainforest |
Q126179050 | Neoisoptera repeatedly colonised Madagascar after the Middle Miocene climatic optimum |
Q114082004 | Nest microhabitats and tree size mediate shifts in ant community structure across elevation in tropical rainforest canopies |
Q115527967 | Nest predation in hole-nesting birds in relation to habitat edge: an experiment |
Q115527970 | Nest predation patterns in ground-nesting passerines on the Iberian Peninsula |
Q115527948 | Nest-predation at the edge: an experimental study contrasting two types of edges in the dry Chaco, Paraguay |
Q115557291 | Nest-predation at the edge: an experimental study contrasting two types of edges in the dry Chaco, Paraguay |
Q58747635 | Nested distributions of bat flies (Diptera: Streblidae) on Neotropical bats: artifact and specificity in host-parasite studies |
Q60347412 | Network analysis by simulated annealing of taxa and islands of Macaronesia (North Atlantic Ocean) |
Q111173422 | Network structure of vertebrate scavenger assemblages at the global scale: drivers and ecosystem functioning implications |
Q111172423 | Networkâscale effects of invasive species on spatiallyâstructured amphibian populations |
Q60507954 | Neutral biogeography of phylogenetically structured interaction networks |
Q129441976 | New methods for measuring ENM breadth and overlap in environmental space |
Q57068145 | New spatial and temporal perspectives on the assembly of biotas and communities. Special issue: International Biogeography Society, 6th biennial International Conference |
Q57068411 | New trends in species distribution modelling |
Q60334556 | Nice weather for bettongs: using weather events, not climate means, in species distribution models |
Q57197596 | Niche and area of distribution modeling: a population ecology perspective |
Q112796921 | Niche breadth and range area in North American trees |
Q56437423 | Niche conservatism among non-native vertebrates in Europe and North America |
Q112800918 | Niche differentiation within a cryptic pathogen complex: climatic drivers and hyperparasitism at multiple spatial scales |
Q112800954 | Niche use and coâoccurrence patterns of zooplankton along a strong urbanization gradient |
Q56936122 | NicheA: creating virtual species and ecological niches in multivariate environmental scenarios |
Q60365099 | NicheMapR - an R package for biophysical modelling: the microclimate model |
Q113109772 | NicheMapR â an R package for biophysical modelling: the ectotherm and Dynamic Energy Budget models |
Q113109676 | NicheMapR â an R package for biophysical modelling: the endotherm model |
Q125747466 | Niches in the Anthropocene: passerine assemblages show niche expansion from natural to urban habitats |
Q125883821 | Niches within a niche: ecological differentiation of subterranean amphipods across Europe's interstitial waters |
Q126263304 | Nitrogen deposition enhances Bromus tectorum invasion: biogeographic differences in growth and competitive ability between China and North America |
Q56767584 | No adaptation to altitude in the invasive plantErigeron annuusin the Swiss Alps |
Q117034877 | No biotic homogenisation across decades but consistent effects of landscape position and pH on macrophyte communities in boreal lakes |
Q112800949 | Noctuid and geometrid moth assemblages show divergent elevational gradients in body size and color lightness |
Q60539585 | Nomadism and seasonal range expansion in a large frugivorous bird |
Q56058816 | Non flying mammals and landscape changes in the tropical rain forest region of Los Tuxtlas, Mexico |
Q56437419 | Non-equilibrium in plant distribution models - only an issue for introduced or dispersal limited species? |
Q56426374 | Non-native species modify the isotopic structure of freshwater fish communities across the globe |
Q56836853 | Non-random patterns of invasion and extinction reduce phylogenetic diversity in island bird assemblages |
Q60300067 | Nonstationary effects of productivity, seasonality, and historical climate changes on global amphibian diversity |
Q57068418 | Northern glacial refugia for the pygmy shrew Sorex minutus in Europe revealed by phylogeographic analyses and species distribution modelling |
Q57014231 | Novel methods improve prediction of speciesâ distributions from occurrence data |
Q57052241 | Novel spatial analysis methods reveal scale-dependent spread and infer limiting factors of invasion by Sahara mustard |
Q57205158 | Null Versus Neutral Models: What's The Difference? |
Q57690272 | Number of endemic and native plant species in the Galapagos Archipelago in relation to geographical parameters |
Q114625051 | Numbers of litters, litter size and survival in two species of microtines at two elevations |
Q115527947 | Numerical and dietary responses of a predator community in a temperate zone of Europe |
Q125873198 | Nutrient and water flux in a small arctic watershed: an overview |
Q112796974 | Nutritional ecology of yellow-bellied marmots in the White Mountains of California |
Q57658981 | Nutritional estimate of populations of some wild free-ranging African ungulates in grassland (Nechisar national park, Ethiopia) in dry season |
Q126796531 | Occupancy in dynamic systems: accounting for multiple scales and false positives using environmental DNA to inform monitoring |
Q57950483 | Occupancy-abundance relationships and sampling scales |
Q112796944 | Occupancy-abundance relationships and sampling scales |
Q57262782 | Of niches and distributions: range size increases with niche breadth both globally and regionally but regional estimates poorly relate to global estimates |
Q63628319 | On population abundance and niche structure |
Q56817164 | On the biogeography of seed mass in Germany - distribution patterns and environmental correlates |
Q57069440 | On the generality of habitat distribution models: a case study of capercaillie in three Swiss regions |
Q111289105 | On the integration of biotic interaction and environmental constraints at the biogeographical scale |
Q112801134 | On the packing and filling of functional space in eastern North American tree assemblages |
Q60147985 | On the selection of phylogenetic eigenvectors for ecological analyses |
Q56937437 | On using integral projection models to generate demographically driven predictions of species' distributions: development and validation using sparse data |
Q60334599 | One, two and three-dimensional geometric constraints and climatic correlates of North American tree species richness |
Q122165692 | Ontogenetic changes in the micro-habitat preferences of Decticus verrucivorus (Orthoptera: Tettigoniidae) at the edge of its range |
Q60523863 | Ontogenetic patterns of relative growth in young roach Rutilus rutilus: within-river basin comparisons |
Q112800964 | Onward but not always upward: individualistic elevational shifts of tree species in subtropical montane forests |
Q59701785 | Opening the black box: an open-source release of Maxent |
Q126192958 | Opportunistic data reveal widespread species turnover in Enallagma damselflies at biogeographical scales |
Q112801030 | Opportunistic records reveal Mediterranean reptilesâ scale-dependent responses to anthropogenic land use |
Q60431417 | Opposed latitudinal patterns of network-derived and dietary specialization in avian plant-frugivore interaction systems |
Q57212824 | Opposite shell-coiling morphs of the tropical land snail Amphidromus martensi show no spatial-scale effects |
Q60535884 | Optimal taxonomic groups for biodiversity assessment: a meta-analytic approach |
Q60314658 | Optimising long-term monitoring projects for species distribution modelling: how atlas data may help |
Q27132801 | Over the top: do thermal barriers along elevation gradients limit biotic similarity? |
Q120248186 | Overcoming phylogenetic and geographic uncertainties to test for correlates of range size evolution in gymnophthalmid lizards |
Q123149251 | Oviposition date and pattern of embryogenesis in the grasshopper Chorthippus brunneus (Orthoptera, Acrididae) |
Q122976347 | Oxygen and nitrate respiration in a reed swamp sediment from a eutrophic lake |
Q125917264 | Palatability of silver birch seedlings to root voles Microtus oeconomus |
Q57018412 | PaleoView: a tool for generating continuous climate projections spanning the last 21 000 years at regional and global scales |
Q60237417 | Parasite loads are higher in the tropics: temperate to tropical variation in a single host-parasite system |
Q55841984 | Parasitism and epibiosis in native and non-native gammarids in freshwater in Ireland |
Q55922561 | Parrot claylick distribution in South America: do patterns of âwhereâ help answer the question âwhyâ? |
Q111427208 | Participatory scenarios for restoring European landscapes show a plurality of nature values |
Q57021247 | Partitioning and mapping uncertainties in ensembles of forecasts of species turnover under climate change |
Q115391812 | Partitioning the impact of abiotic factors and spatial patterns on species richness and community structure of ground ant assemblages in four Bornean rainforests |
Q57191274 | Partitioning the variation in African vertebrate distributions into environmental and spatial components - exploring the link between ecology and biogeography |
Q56929446 | Patch configuration affects alpine plant distribution |
Q60529787 | Patch size, shape and edge distance influence seed predation on a palm species in the Atlantic forest |
Q92097231 | Pathogeography: leveraging the biogeography of human infectious diseases for global health management |
Q112605381 | Pathways of tundra encroachment by trees and tall shrubs in the western Brooks Range of Alaska |
Q57035230 | Pattern of local plant species richness along a gradient of landscape topographical heterogeneity: result of spatial mass effect or environmental shift? |
Q60509699 | Patterns and drivers of aquatic invertebrate diversity across an arid biome |
Q67233300 | Patterns in species richness, size, and latitudinal range of East Atlantic fishes |
Q56157239 | Patterns in woody species diversity, richness and partitioning of diversity in forest communities of tropical deciduous forest biome |
Q126046761 | Patterns of abundance and demography: Collembola in a habitat patch gradient |
Q56556896 | Patterns of bird invasion are consistent with environmental filtering |
Q56550430 | Patterns of change over time in darter (Teleostei: Percidae) assemblages of the Arkansas River basin, northeastern Oklahoma, USA |
Q57054691 | Patterns of commonness and rarity in central European birds: reliability of the core-satellite hypothesis within a large scale |
Q114165570 | Patterns of endemic extinctions among island bird species |
Q57247138 | Patterns of host use in solitary parasitoids (Hymenoptera, Ichneumonidae): field evidence from a homogeneous habitat |
Q57056014 | Patterns of invertebrate density and taxonomic richness across gradients of area, isolation, and vegetation diversity in a lake-island system |
Q56879754 | Patterns of island treeline elevation - a global perspective |
Q56417907 | Patterns of niche filling and expansion across the invaded ranges of an Australian lizard |
Q56833200 | Patterns of parasite species richness of Western Palaeartic micro-mammals: island effects |
Q60581490 | Patterns of plant beta-diversity along elevational and latitudinal gradients in mountain forests of China |
Q111172465 | Patterns of plant naturalization show that facultative mycorrhizal plants are more likely to succeed outside their native Eurasian ranges |
Q56946117 | Patterns of rare fish and aquatic insects in a southwestern French river catchment in relation to simple physical variables |
Q60495322 | Patterns of resource tracking by avian frugivores at multiple spatial scales: two case studies on discordance among scales |
Q60550867 | Patterns of species richness in dry grassland patches in an agricultural landscape |
Q123259855 | Patterns of turtle speciesâgeographic range size and a test of Rapoport's rule |
Q59883064 | Peatland forests are the least diverse tree communities documented in Amazonia, but contribute to high regional beta-diversity |
Q57209697 | Performance tradeoffs in target-group bias correction for species distribution models |
Q110710816 | Periphyton, chlorophyll a, and diatoms of the Middle Fork of the Salmon River, Idaho |
Q125744973 | Perspectives and challenges for the use of radar in biological conservation |
Q73173816 | Phenological Predictability Index in BRAHMS: a tool for herbarium-based phenological studies |
Q59270381 | Phenological shifts in hoverflies (Diptera: Syrphidae): linking measurement and mechanism |
Q112800948 | Phenology in freshwaters: a review and recommendations for future research |
Q112801104 | PhyloMeasures: a package for computing phylogenetic biodiversity measures and their statistical moments |
Q57013954 | Phylogenetic alpha and beta diversities of butterfly communities correlate with climate in the western Swiss Alps |
Q128825627 | Phylogenetic and compositional diversity are governed by different rules: a study of fleas parasitic on small mammals in four biogeographic realms |
Q57122358 | Phylogenetic and functional diversity area relationships in two temperate forests |
Q112801115 | Phylogenetic clustering increases with succession for lianas in a Chinese tropical montane rain forest |
Q112796934 | Phylogenetic community structure and phylogenetic turnover across space and edaphic gradients in western Amazonian tree communities |
Q56965651 | Phylogenetic community structure in Minnesota oak savanna is influenced by spatial extent and environmental variation |
Q112801092 | Phylogenetic community structure metrics and null models: a review with new methods and software |
Q56832452 | Phylogenetic composition and structure of tree communities shed light on historical processes influencing tropical rainforest diversity |
Q113798981 | Phylogenetic composition of native island floras influences naturalized alien species richness |
Q112800997 | Phylogenetic conservatism and biogeographic affinity influence woody plant species richnessâclimate relationships in eastern Eurasia |
Q60198443 | Phylogenetic diversity, types of endemism and the evolutionary history of New World bats |
Q60380846 | Phylogenetic effects on functional traits and life history strategies of Australian freshwater fish |
Q57063306 | Phylogenetic generalised dissimilarity modelling: a new approach to analysing and predicting spatial turnover in the phylogenetic composition of communities |
Q112796909 | Phylogenetic imputation of plant functional trait databases |
Q112800938 | Phylogenetic niche conservatism and variations in species diversityâclimate relationships |
Q60549065 | Phylogenetic properties of Tertiary relict flora in the east Asian continental islands: imprint of climatic niche conservatism and in situ diversification |
Q57021219 | Phylogenetic signals in the climatic niches of the world's amphibians |
Q112800995 | Phylogenetic structure of angiosperm trees in local forest communities along latitudinal and elevational gradients in eastern North America |
Q55869419 | Phylogeny and biogeography of Oriolidae (Aves: Passeriformes) |
Q58052172 | Phylogeny and species traits predict bird detectability |
Q59941803 | Phylogeography: spanning the ecology-evolution continuum |
Q111172437 | Physiology in ecological niche modeling: using zebra mussel's upper thermal tolerance to refine model predictions through Bayesian analysis |
Q64032093 | Phytogeographical evidence for post-glacial dispersal limitation of European beech forest species |
Q125891644 | Phytoplankton production in relation to physicoâchemical conditions in a small, oligotrophic subarctic lake in South Greenland |
Q124844659 | Phytoâ and necromass above and below ground in a fen |
Q125945591 | Piosphere contribution to landscape heterogeneity: a case study of remoteâsensed woody cover in a high elephant density landscape |
Q112796953 | Plant colonisation in small forest-floor patches: importance of plant group and disturbance traits |
Q109936190 | Plant colonization of bare peat surface - relative importance of seed availability and soil |
Q63388672 | Plant diversity in Oceanic archipelagos: realistic patterns emulated by an agentâbased computer simulation |
Q126099116 | Plant invasion in Mediterranean Europe: current hotspots and future scenarios |
Q56771854 | Plant invasions along mountain roads: the altitudinal amplitude of alien Asteraceae forbs in their native and introduced ranges |
Q120016257 | Plant niches along the water-table gradient on an ombrotrophic mire expanse |
Q57207997 | Plant performance in central and northern peripheral populations of the widespreadPlantago coronopus |
Q57194101 | Plant population patterns in a glacier foreland succession: pioneer herbs and later-colonizing shrubs |
Q104206229 | Plant responses to livestock grazing frequency in an Australian temperate grassland |
Q113173492 | Plant species coexistence and dispersion of seed traits in a grassland |
Q112814411 | Plant species diversity and grazing in the Scandinavian mountains - patterns and processes at different spatial scales |
Q60533011 | Plant species response to land use change -Campanula rotundifolia,Primula verisandRhinanthus minor |
Q60550865 | Plant species richness in grasslands: the relative importance of contemporary environment and land-use history since the Iron Age |
Q57025604 | Plant-pollinator networks in semi-natural grasslands are resistant to the loss of pollinators during blooming of mass-flowering crops |
Q64032129 | Plants on small islands revisited: the effects of spatial scale and habitat quality on the speciesâarea relationship |
Q60543422 | Plants show more flesh in the tropics: variation in fruit type along latitudinal and climatic gradients |
Q112079105 | Plasticity in age and size at metamorphosis in Rana temporaria - comparison of high and low latitude populations |
Q55882794 | Pleistocene megafaunal extinctions and the functional loss of long-distance seed-dispersal services |
Q57068472 | Plio-Pleistocene climate change and geographic heterogeneity in plant diversity-environment relationships |
Q123020955 | Polar deserts, their plant cover and plant production in the Canadian High Arctic |
Q125404167 | Pollinator competition and the structure of floral resources |
Q126026653 | Population and community level responses in Anas âspecies to patch disturbance caused by an ecosystem engineer, the beaver |
Q60459045 | Population biology of the weasel Mustela nivalis on British game estates |
Q115557288 | Population changes of different predators during a water vole cycle in a central European mountainous habitat |
Q56422940 | Population cycles produce periodic range boundary pulses |
Q110792395 | Population density and species composition of moss-living tardigrades in a boreo-nemoral forest |
Q112279631 | Population dynamics (1869-1994), demography, and home ranges of the lynx in Bialowieza Primeval Forest (Poland and Belarus) |
Q60160851 | Population fluctuations and habitat selection in the Eurasian red squirrel Sciurus vulgaris |
Q57248582 | Population persistence in a landscape context: the case of endangered arctic fox populations in Fennoscandia |
Q57251420 | Population resilience to an extreme drought is influenced by habitat area and fragmentation in the local landscape |
Q57267257 | Population structure and adult plant performance of forest herbs in three contrasting habitats |
Q60233546 | Population structure and migratory directions of Scandinavian bluethroatsLuscinia svecica- a molecular, morphological and stable isotope analysis |
Q57049127 | Population trends in black woodpecker in relation to changes and characteristics of European forests |
Q110790962 | Population variability among three small mammal species in the semiarid Neotropics: the role of density-dependent and density-independent factors |
Q112800956 | Populations of highâvalue predators reflect the traits of their prey |
Q57008500 | Post-fire recovery of ant communities in Submediterranean Pinus nigra forests |
Q57068509 | Postglacial dispersal limitation of widespread forest plant species in nemoral Europe |
Q123313950 | Postglacial recolonization of North America by spadefoot toads: integrating niche and corridor modeling to study speciesâ range dynamics over geologic time |
Q114082005 | Postâfire vegetation and climate dynamics in lowâelevation forests over the last three millennia in Yellowstone National Park |
Q57068619 | Potential impact of climatic change on the distribution of forest herbs in Europe |
Q112801078 | Potential trajectories of old-growth Neotropical forest functional composition under climate change |
Q60114591 | Prairie dog presence affects occurrence patterns of disease vectors on small mammals |
Q115527973 | Predation and competition within an assemblage of larval newts (Triturus) |
Q109061739 | Predation and potential transfer of pollen in a population of Saxifraga hirculus |
Q115527981 | Predation on amphibian eggs and tadpoles by common predators in acidified lakes |
Q55842196 | Predation on artificial bird nests along an urban gradient: predatory risk or relaxation in urban environments? |
Q115527960 | Predation on artificial bird nests along an urban gradient: predatory risk or relaxation in urban environments? |
Q109943895 | Predation on artificial ground nests in relation to forest fragmentation, agricultural land and habitat structure |
Q115527964 | Predation on artificial nests in a forest dominated landscape - the effects of nest type, patch size and edge structure |
Q115527968 | Predation on artificial nests in relation to forest type: contrasting the use of quail and plasticine eggs |
Q115527991 | Predation on brown hare and ring-necked pheasant populations in southern Sweden |
Q115527977 | Predation on rodents in Bialowieza primeval forest, Poland |
Q115557282 | Predation rate on artificial nests increases with human housing density in suburban habitats |
Q115527954 | Predator control and the density and reproductive success of grouse populations in Finland |
Q60311236 | Predator identification methods in diet studies: uncertain assignment produces biased results? |
Q115527961 | Predator-prey interactions between brown trout Salmo trutta and native and introduced ampbipods; tbeir implications for fisb diets |
Q115533047 | Predator-rodent-plant interactions along a coast-inland gradient in Fennoscandian tundra |
Q115533031 | Predatorâprey overlap in three dimensions: cod benefit from capelin coming near the seafloor |
Q60557856 | Predictability of stream insect distributions is dependent on niche position, but not on biological traits or taxonomic relatedness of species |
Q121159543 | Predicted distributions and abundances of the sea turtle âlost yearsâ in the western North Atlantic Ocean |
Q63564059 | Predicted trajectories of tree community change in Amazonian rainforest fragments |
Q112801018 | Predicting biodiversity loss in island and countryside ecosystems through the lens of taxonomic and functional biogeography |
Q57013963 | Predicting current and future spatial community patterns of plant functional traits |
Q57114101 | Predicting ecosystem functions from biodiversity and mutualistic networks: an extension of trait-based concepts to plant-animal interactions |
Q57014128 | Predicting future distributions of mountain plants under climate change: does dispersal capacity matter? |
Q57068478 | Predicting future shifts in species diversity |
Q124880401 | Predicting global population connectivity and targeting conservation action for snow leopard across its range |
Q57268826 | Predicting krill swarm characteristics important for marine predators foraging off East Antarctica |
Q57251257 | Predicting microscale shifts in the distribution of the butterfly Plebejus argus at the northern edge of its range |
Q128364879 | Predicting niche overlap with modelâbased ordination |
Q56779909 | Predicting patterns of plant species richness in megadiverse South Africa |
Q64031949 | Predicting plant species distribution patterns using simple climatic parameters: a case study of Ecuadorian palms |
Q123201452 | Predicting predatorâprey interactions in terrestrial endotherms using random forest |
Q60116600 | Predicting range expansion of an ectoparasite - the effect of spring and summer temperatures on deer ked Lipoptena cervi (Diptera: Hippoboscidae) performance along a latitudinal gradient |
Q60510855 | Predicting range shifts under global change: the balance between local adaptation and dispersal |
Q126111312 | Predicting rat presence on small islands |
Q125986296 | Predicting species abundance by implementing the ecological niche theory |
Q73173815 | Predicting species distributions based on incomplete survey data: the trade-off between precision and scale |
Q57021436 | Predicting species diversity with ED: the quest for evidence |
Q120016251 | Predicting the future of species diversity: macroecological theory, climate change, and direct tests of alternative forecasting methods |
Q110630337 | Predicting the invasion success of Mediterranean alien plants from their introduction characteristics |
Q110789465 | Predicting the nonâlinear collapse of plantâfrugivore networks due to habitat loss |
Q56773238 | Predicting the spread of an invasive plant: combining experiments and ecological niche model |
Q115527939 | Predicting top predator habitats in the Southwest Indian Ocean |
Q56752601 | Predicting worldwide invasiveness for four major problematic decapods: an evaluation of using different calibration sets |
Q62660695 | Predictive modelling of tree species distributions on the Iberian Peninsula during the Last Glacial Maximum and Mid-Holocene |
Q57579456 | Predictive models of habitat preferences for the Eurasian eagle owlBubo bubo: a multiscale approach |
Q60363417 | Predictors of Phytophthora diversity and community composition in natural areas across diverse Australian ecoregions |
Q57021426 | Presence-absence versus presence-only modelling methods for predicting bird habitat suitability |
Q126009674 | Prey responses to foxes are not determined by nativeness |
Q115038446 | Prey selection in coastal Eurasian otters Lutra Iutra |
Q110848134 | Primary productivity and biomass of epiphytes on Phragmites australis in a eutrophic Danish lake |
Q57197023 | Primary productivity and species richness: relationships among functional guilds, residency groups and vagility classes at multiple spatial scales |
Q62927372 | Prioritizing global marine mammal habitats using density maps in place of range maps |
Q56386674 | Process from pattern in the distribution of an endangered leaf beetle |
Q58896657 | Process-based long-term evaluation of an ecological network of calcareous grasslands connected by sheep herding |
Q56959930 | Processes of community assembly in an environmentally heterogeneous, high biodiversity region |
Q113355691 | Production and population dynamics of Leptodiaptomus sicilis in a mountain lake in Alberta, Canada |
Q57068225 | Productivity-diversity patterns in arctic tundra vegetation |
Q58101208 | Projected climate change causes loss and redistribution of genetic diversity in a model metapopulation of a medium-good disperser |
Q60364481 | Projected distributions of Southern Ocean albatrosses, petrels and fisheries as a consequence of climatic change |
Q58063081 | Projected impacts of climate warming on the functional and phylogenetic components of coastal Mediterranean fish biodiversity |
Q114082002 | Projected migrations of southern Indian Ocean albatrosses as a response to climate change |
Q129219523 | Projecting community trophic structures for the last 120 000 years |
Q126920270 | Pronounced changes of subterranean biodiversity patterns along a Late Pleistocene glaciation gradient |
Q56771318 | Properties of native plant communities do not determine exotic success during early forest succession |
Q57014055 | Prospective sampling based on model ensembles improves the detection of rare species |
Q110267837 | Proximity and abundance of mother trees affects recruitment patterns in a longâterm tropical forest restoration study |
Q109351310 | Qualitative geographical variation in interspecific interactions |
Q56961408 | Quantifying island isolation - insights from global patterns of insular plant species richness |
Q60559612 | Quantifying non-breeding season occupancy patterns and the timing and drivers of autumn migration for a migratory songbird using Doppler radar |
Q58729388 | Quantifying spatial classification uncertainties of the historical Wisconsin landscape (USA) |
Q111264031 | Quantifying the climatic niche of symbiont partners in a lichen symbiosis indicates mutualist-mediated niche expansions |
Q56771323 | Quantifying the potential effects of climate change and the invasion of smallmouth bass on native lake trout populations across Canadian lakes |
Q57015411 | Quantifying the randomness of extinctions |
Q114145324 | Quantifying the randomness of extinctions |
Q57021276 | Quaternary climate changes explain diversity among reptiles and amphibians |
Q117025702 | Quaternary refugia are associated with higher speciation rates in mammalian faunas of the Western Palaearctic |
Q115533035 | Questioning assumptions of trophic behavior in a broadly ranging marine predator guild |
Q60298984 | Quo vadis amphibia? Global warming and breeding phenology in frogs, toads and salamanders |
Q114981842 | RSDB: an easy to deploy openâsource web platform for remote sensing raster and point cloud data management, exploration and processing |
Q126840828 | Radar aeroecology â a missing piece of the puzzle for studying the migration ecology of animals |
Q60400246 | Rainfall, geology and landscape position generate large-scale spatiotemporal fire pattern heterogeneity in an African savanna |
Q123363078 | Random mating in a boreal population of European common frogs Rana temporaria |
Q60488583 | Random processes and geographic species richness patterns: why so few species in the north? |
Q31102933 | Range and niche shifts in response to past climate change in the desert horned lizard (Phrynosoma platyrhinos). |
Q128279048 | Range area matters, and so does spatial configuration: predicting conservation status in vertebrates |
Q59124031 | Range expansion and retraction along a moving contact zone has no effect on the genetic diversity of two passerine birds |
Q60147906 | Range size patterns in European freshwater trematodes |
Q60362612 | Ranking the ecological causes of dispersal in a butterfly |
Q57662378 | Rapid altitudinal migration of mountain plants in Taiwan and its implications for high altitude biodiversity |
Q57231648 | Rarefaction method for assessing plant species diversity on a regional scale |
Q104879916 | Rarity and species/area relationships of vascular plants in deciduous woods, western Norway - applications to nature reserve selection |
Q112796951 | Rarity within taxonomie lineages and the use of taxa above the level of species |
Q56383708 | Reconstructing changes in the genotype, phenotype, and climatic niche of an introduced species |
Q120969546 | Reconstruction of the historical range alters niche estimates in an endangered rodent |
Q57616183 | Red herrings remain in geographical ecology: a reply to Hawkins et al. (2007) |
Q58040631 | Red herrings revisited: spatial autocorrelation and parameter estimation in geographical ecology |
Q60148034 | Red herrings revisited: spatial autocorrelation and parameter estimation in geographical ecology |
Q59197934 | Red squirrels decline in abundance in the boreal forests of Finland and NW Russia |
Q112852569 | Redlistr: tools for the IUCN Red Lists of ecosystems and threatened species in R |
Q114146159 | Reductions in connectivity and habitat quality drive local extinctions in a plant diversity hotspot |
Q120686471 | Reflections on niches and numbers |
Q111376367 | Regenerative traits of tree species in a deciduous forest of northeastern North America |
Q58656646 | Regional and global elevational patterns of microbial species richness and evenness |
Q60495308 | Regional vs local effects of habitat loss and fragmentation on two plant-animal interactions |
Q57437371 | Regional-scale patterns of soil microbes and nematodes across grasslands on the Mongolian plateau: relationships with climate, soil, and plants |
Q57409702 | Relating mesocarnivore relative abundance to anthropogenic land-use with a hierarchical spatial count model |
Q110790961 | Relating species density to environmental variables in presence of spatial autocorrelation: a study case on soil nematodes distribution |
Q120016282 | Relationship between the seed rain and the establishment of vegetation in two areas abandoned after peat harvesting |
Q57056090 | Relationships among ecological traits of wild bee communities along gradients of habitat amount and fragmentation |
Q57008189 | Relationships among taxonomic, functional, and phylogenetic ant diversity across the biogeographic regions of Europe |
Q60449996 | Relationships between body size and geographical range size among Australian mammals: has human impact distorted macroecological patterns? |
Q56936956 | Relative importance of climate vs local factors in shaping the regional patterns of forest plant richness across northeast China |
Q110762749 | Relative importance of different dispersal vectors for small aquatic invertebrates in a rock pool metacommunity |
Q57002189 | Relative importance of resource quantity, isolation and habitat quality for landscape distribution of a monophagous butterfly |
Q60581492 | Relative influence of regional species richness vs local climate on local species richness in China's forests |
Q64032140 | Relative role of contemporary environment versus history in shaping diversity patterns of China's woody plants |
Q110295748 | Relics of beavers past: time and population density drive scaleâdependent patterns of ecosystem engineering |
Q114081991 | Remotelyâsensed slowing down in spatially patterned dryland ecosystems |
Q55845485 | Replacement of the native crayfish Astacus astacus by the introduced species Pacifastacus leniusculus in a small, enclosed Finnish lake: a 30-year study |
Q57262621 | Representing genetic variation as continuous surfaces: an approach for identifying spatial dependency in landscape genetic studies |
Q60469523 | Reproducibility of the multi-component aspect of species diversity across different areas and scales: towards the constitution of a shortlist of complementary indices for monitoring fish diversity? |
Q56976284 | Reproduction as a bottleneck to treeline advance across the circumarctic forest tundra ecotone |
Q115038452 | Reproduction of the white-tailed sea eagle Haliaeetus albicilla in Sweden |
Q126014395 | Reproductive biology of the arctic collembolan Hypogastrura tullbergi |
Q60583440 | Reproductive differentiation in a Saxifraga hirculus population along an environmental gradient on a central Swedish mire |
Q125825364 | Reproductive ecology of the boreal riparian guild of Drosophila |
Q126086282 | Reproductive effort in cotton grass tussock tundra |
Q56986647 | Reproductive patterns in central and marginal populations of a large brown seaweed: drastic changes at the southern range limit |
Q60456576 | Reproductive success, mortality and sexual size dimorphism in the adder, Vipera berus |
Q115038441 | Reproductive timing in Eurasian otters on the coast of Norway |
Q112796964 | Reproductive variability and pollen limitation in three Betula taxa in northern Sweden |
Q115038454 | Residue levels of organochlorine and mercury compounds in unhatched eggs and the relationships to breeding success in white-tailed sea eagles Haliaeetus albicilla in Sweden |
Q112784395 | Resilience of fishes and invertebrates to prolonged drought in two California streams |
Q57055963 | Resource heterogeneity does not explain the diversity-productivity relationship across a boreal island fertility gradient |
Q121007804 | Resource heterogeneity influences home range area in the swamp wallaby Wallabia bicolor |
Q60513453 | Resource partitioning of roach Rutilus rutilus and bleak Alburnus alburnus in two eutrophic lakes in SE Norway |
Q57269776 | Resource separation analysis with moose indicates threats to caribou in human altered landscapes |
Q126224805 | Resource utilization by bumblebee queens, workers and males in a subarctic area |
Q56853182 | Respiration and energetics of the bumblebee Bombus terrestris queen |
Q60580643 | Response by coypus to catastrophic events of cold and flooding |
Q60558488 | Response of Microtus pennsylvanicus to vegetation fertilized with various nutrients, with particular emphasis on sodium and nitrogen concentrations in plant tissues |
Q56340625 | Response of a raptor community to shrinking area and degradation of tropical rain forest in the south western Ghats (India) |
Q57008310 | Response of ant functional composition to fire |
Q112798860 | Response of collembolan communities to land-use change and grassland succession |
Q112606190 | Response of marine communities to local temperature changes |
Q57051976 | Response of tree seedlings to the abiotic heterogeneity generated by nurse shrubs: an experimental approach at different scales |
Q57019917 | Response to Comment on âMethods to account for spatial autocorrelation in the analysis of species distributional data: a reviewâ |
Q56961763 | Response to comments on Species diversity can drive speciation |
Q58259787 | Responses of alpine shrubs to simulated environmental change during three years in the mid-latitude mountain, northern Japan |
Q125271718 | Responses of alpine shrubs to simulated environmental change during three years in the midâlatitude mountain, northern Japan |
Q60445618 | Responses of nectar-feeding birds to floral resources at multiple spatial scales |
Q55839688 | Responses of vegetation to a changing regime of disturbance: effects of feral pigs in a Californian coastal prairie |
Q112801029 | Restoration potential of threatened ecosystem engineers increases with aridity: broad scale effects on soil nutrients and function |
Q57245797 | Restricted habitat use by an African savanna herbivore through the seasonal cycle: key resources concept expanded |
Q60496975 | Rethinking edge effects: the unaccounted role of geometric constraints |
Q111172409 | Rethinking the scale and formulation of indices assessing organism vulnerability to warmer habitats |
Q57021044 | Retracted: Lizards could be warming faster than climate |
Q57021053 | Retraction: âLizards could be warming faster than climateâ by Ferri-YĂĄĂąez, F. and AraĂşjo, M. B |
Q60550821 | Revealing patterns of nocturnal migration using the European weather radar network |
Q57716186 | Reversing habitat loss: deciduous habitat fragmentation matters to birds in a larch plantation matrix |
Q125123126 | Revisiting longâdistance dispersal in a coastal marine fish |
Q112801011 | Revisiting the dimensionality of biological diversity |
Q58804426 | Road and topography effects on invasion: edge effects in rat foraging patterns in two oceanic island forests (Tenerife, Canary Islands) |
Q114080273 | Road and topography effects on invasion: edge effects in rat foraging patterns in two oceanic island forests (Tenerife, Canary Islands) |
Q55980104 | Robustness despite uncertainty: regional climate data reveal the dominant role of humans in explaining global extinctions of Late Quaternary megafauna |
Q115527979 | Rodent seed predation in cereal crop areas of central Spain: effects of physiognomy, food availability, and predation risk |
Q60549069 | Role of climate and geohistorical factors in driving plant richness patterns and endemicity on the east Asian continental islands |
Q60148007 | SAM: a comprehensive application for Spatial Analysis in Macroecology |
Q57232155 | SIDER: an R package for predicting trophic discrimination factors of consumers based on their ecology and phylogenetic relatedness |
Q113110139 | SSP: an R package to estimate sampling effort in studies of ecological communities |
Q112800914 | Sahul's megafauna were vulnerable to plantâcommunity changes due to their position in the trophic network |
Q60466174 | Salinity influences the distribution of marine snakes: implications for evolutionary transitions to marine life |
Q59293050 | Sampled-based estimation of diversity sensu stricto by transforming Hurlbert diversities into effective number of species |
Q112800926 | Sampling biases shape our view of the natural world |
Q119581340 | Sampling design may obscure speciesâarea relationships in landscapeâscale field studies |
Q57193867 | Sampling in ecology and evolution - bridging the gap between theory and practice |
Q58740322 | Scale dependence of diversity measures in a leaf-litter ant assemblage |
Q60117179 | Scale dependency and functional response in moose habitat selection |
Q112796910 | Scale dependency in the functional form of the distance decay relationship |
Q126920402 | Scale dependency of community assembly differs between coastal marine bacteria and fungi |
Q57018492 | Scale dependency of metapopulation models used to predict climate change impacts on small mammals |
Q58192859 | Scale dependency of processes structuring metacommunities of cladocerans in temporary pools of High-Andes wetlands |
Q112796394 | Scale dependent diversity patterns in arboreal and terrestrial oribatid mite (Acari: Oribatida) communities |
Q56158041 | Scale of habitat connectivity and colonization in fragmented nuthatch populations |
Q57577522 | Scale of habitat connectivity and colonization in fragmented nuthatch populations |
Q114627651 | Scale of inference: on the sensitivity of habitat models for wide-ranging marine predators to the resolution of environmental data |
Q118114441 | Scale-dependence of phylogenetic signal in ecological traits of ectoparasites |
Q57057249 | Scale-dependent effects of land use on plant species richness of mountain grassland in the European Alps |
Q112801033 | Scale-dependent spatial patterns in benthic communities around a tropical island seascape |
Q64032333 | Scale-dependent thermal tolerance variation in Australian mountain grasshoppers |
Q118114479 | Scale-invariance of niche breadth in fleas parasitic on small mammals |
Q60507876 | Scale-sensitive landscape complementation determines habitat suitability for a territorial generalist |
Q125404129 | Scaleâdependent effects of landscape structure on pollinator traits, species interactions and pollination success |
Q56777347 | Seabird life histories and climatic fluctuations: a phylogenetic-comparative time series analysis of North Atlantic seabirds |
Q60394840 | Searching for the fundamental niche using individual-based habitat selection modelling across populations |
Q120016407 | Seasonal changes in census efficiency of birds at marshes and fen mires in southern Sweden |
Q115557287 | Seasonal changes in the numerical responses of predators to cyclic vole populations |
Q60441489 | Seasonal community structure of macromycetes in Veracruz, Mexico |
Q115527990 | Seasonal crayfish activity as influenced by fluctuating water levels and presence of a fish predator |
Q56556242 | Seasonal drought limits tree species across the Neotropics |
Q115527992 | Seasonal dynamics of small vagile predators on a marine shallow soft bottom |
Q111376357 | Seasonal use by birds of stream-side riparian habitat in coniferous forest of northcentral British Columbia |
Q107075205 | Seasonality, niche management and vertical migration in landscapes of relief |
Q57011110 | Secondary succession and summer herbivory in a subarctic grassland: community structure and diversity |
Q110704746 | Seed bank build-up in small disturbances in a Mediterranean pasture: the contribution of endozoochorous dispersal by rabbits |
Q58326198 | Seed dispersal and seedling establishment ofRhus trichocarpapromoted by a crow (Corvus macrorhynchos) on a volcano in Japan |
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Q112796959 | Seed production, predation and dispersal in the Mediterranean myrmecochore Euphorbia characias (Euphorbiaceae) |
Q126044673 | Seedling density and seedling survival in Alaskan cotton grass tussock tundra |
Q113798994 | Seedling responses to decreased snow depend on canopy composition and smallâmammal herbivore presence |
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Q112796916 | Selecting from correlated climate variables: a major source of uncertainty for predicting species distributions under climate change |
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Q112814407 | Selectivity by moose vs the spatial distribution of aspen: a natural experiment |
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Q113685531 | Severity of deforestation mediates biotic homogenisation in an island archipelago |
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Q58478914 | Sex- and age-dependent effects of population density on life history traits of red deer Cervus elaphus in a temperate forest |
Q57237023 | Sexual patterns of prebreeding energy reserves in the common frogRana temporariaalong a latitudinal gradient |
Q57247843 | Shared environmental responses drive co-occurrence patterns in river bird communities |
Q125591837 | Shellfish subsidies along the Pacific coast of North America |
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Q114081993 | Shifting fish distributions impact predation intensity in a subâArctic ecosystem |
Q57004863 | Shifts in trait means and variances in North American tree assemblages: species richness patterns are loosely related to the functional space |
Q115527978 | Shorebird predation may cause discrete generations in an amphipod prey |
Q111172408 | Shorebirds as important vectors for plant dispersal in Europe |
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Q110704754 | Short-term and long-term variation in seed bank/vegetation relations along an environmental and successional gradient |
Q113345349 | Shrews on small islands: epigenetic variation elucidates population stability |
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Q57013759 | Simulated shifts in trophic niche breadth modulate range loss of alpine butterflies under climate change |
Q111172507 | SiteOpt: an openâsource Râpackage for site selection and portfolio optimization |
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Q128573983 | Size matters in quantitative radar monitoring of animal migration: estimating monitored volume from wingbeat frequency |
Q110704834 | Size traits and site conditions determine changes in seed bank structure caused by grazing exclusion in semiarid annual plant communities |
Q112814408 | Size-dependent species-area relationships in benthos: is the world more diverse for microbes? |
Q57011160 | Small-scale dynamics and species richness in successional alvar plant communities |
Q57011077 | Small-scale plant species richness in calcareous grasslands determined by the species pool, community age and shoot density |
Q111172421 | Soil biota composition and the performance of a noxious weed across its invaded range |
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Q121222405 | Soil phytoliths as evidence for species replacement in grazed rangelands of central Argentina |
Q112800972 | Source pools and disharmony of the world's island floras |
Q114627163 | Spatial analysis of an invasion front ofAcer platanoides: dynamic inferences from static data |
Q112801057 | Spatial and temporal heterogeneity in climate change limits species' dispersal capabilities and adaptive potential |
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Q115527953 | Spatial and temporal patterns of seed predation on three tree species in an oak-pine forest |
Q58388958 | Spatial and temporal variation in species-area relationships in the Fynbos biological hotspot |
Q56933778 | Spatial and temporal variation in the morphology (and thus, predicted impact) of an invasive species in Australia |
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Q57201104 | Spatial co-occurrence networks predict the feeding histories of polyphagous arthropod predators at field scales |
Q57248222 | Spatial conservation priorities are highly sensitive to choice of biodiversity surrogates and species distribution model type |
Q57614279 | Spatial determinants of infection risk in a multi-species avian malaria system |
Q60345283 | Spatial distribution and environmental correlates of Australian snubfin and Indo-Pacific humpback dolphins |
Q58750647 | Spatial distribution and habitat selection in coexisting species of mountain ungulates |
Q57245799 | Spatial ecology of large herbivore populations |
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Q115533042 | Spatial extinction or persistence: landscape-temperature interactions perturb predator-prey dynamics |
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Q57263463 | Spatial mismatch in morphological, ecological and phylogenetic diversity, in historical and contemporary European freshwater fish faunas |
Q112800981 | Spatial modelling of ecological indicator values improves predictions of plant distributions in complex landscapes |
Q60346975 | Spatial modelling of species turnover identifies climate ecotones, climate change tipping points and vulnerable taxonomic groups |
Q114625047 | Spatial modelling of the barn owl Tyto alba habitat using landscape characteristics derived from SPOT data |
Q57001987 | Spatial organisation and dynamics of the pine marten Martes martes population in BiaĹowieza Forest (E Poland) compared with other European woodlands |
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Q57122719 | Spatial pattern of adult trees and the mammal-generated seed rain in the Iberian pear |
Q57122987 | Spatial patterns and competition of tree species in a Douglas-fir chronosequence on Vancouver Island |
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Q125589151 | Spatial predictors of fish species composition in European lowland lakes |
Q57263470 | Spatial range shape drives the grain size effects in species distribution models |
Q110762412 | Spatial relationships in a dendritic network: the herpetofaunal metacommunity of the Mattole River catchment of northwest California |
Q60534454 | Spatial risk assessment of livestock exposure to pumas in Patagonia, Argentina |
Q126035704 | Spatial scale, topography and thermoregulatory behaviour interact when modelling speciesâ thermal niches |
Q59154689 | Spatial scaling and transition in pneumatophore arthropod communities |
Q57021549 | Spatial scaling of species abundance distributions |
Q106666808 | Spatial scaling properties of coral reef benthic communities |
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Q113345910 | Spatial synchrony in stream fish populations: influence of species traits |
Q113272089 | Spatial uncertainty in herbarium data: simulated displacement but not error distance alters estimates of phenological sensitivity to climate in a widespread California wildflower |
Q56934018 | Spatial variability and abiotic determinants of termite mounds throughout a savanna catchment |
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Q56358620 | Spatial variation in Allee effects influences patterns of range expansion |
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Q118114490 | Spatial variation in population density across the geographical range in helminth parasites of yellow perch Perca flavescens |
Q115533051 | Spatial variation in vegetation damage relative to primary productivity, small rodent abundance and predation |
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Q112800936 | Spatially explicit models for decisionâmaking in animal conservation and restoration |
Q60367633 | Spatio-temporal analysis of an invasive plant pathogen (Phytophthora ramorum) in England and Wales |
Q114624999 | Spatio-temporal covariation in abundance between the cyclic common vole Microtus arvalis and other small mammal prey species |
Q115533046 | Spatio-temporal dynamics of a tree-killing beetle and its predator |
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Q126082703 | Spatiotemporal food web dynamics along a desert riparianâupland transition |
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Q56969056 | Species distribution models in climate change scenarios are still not useful for informing policy planning: an uncertainty assessment using fuzzy logic |
Q110259924 | Species distribution models rarely predict the biology of real populations |
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Q112800935 | Species interactions: nextâlevel citizen science |
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Q60462740 | Species richness and diversity in different functional groups across environmental stress gradients: a model for marine rocky shores |
Q113794766 | Species richness in mammalian herbivores: patterns in the horeal zone |
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Q112800933 | Speciesâlevel CWM values mask contrasting intraâ versus interspecific trait shifts at subtropical forest edges |
Q126085993 | Speciesâhabitat associations and demographic rates of forest trees |
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Q120016260 | Sphagnum mosses as a microhabitat for invertebrates in acidified lakes and the colour adaptation and substrate preference in Leucorrhinia dubia (Odonata, Anisoptera) |
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Q56982185 | Spore deposition of wood-decaying fungi: importance of landscape composition |
Q126037721 | Spore rain in relation to regional sources and beyond |
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Q114625031 | Spruce-fir growth form changes in the forest-tundra ecotone of Rocky Mountain National Park, Colorado, USA |
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Q113798984 | Stable species and interactions in plantâpollinator networks deviate from core position in fragmented habitats |
Q111425487 | Stand structure, variability in growth and intraspecific competition in a peatland stand of black spruce Picea mariana |
Q57019919 | Static species distribution models in dynamically changing systems: how good can predictions really be? |
Q124988506 | Statistical approaches in landscape genetics: an evaluation of methods for linking landscape and genetic data |
Q56068320 | Stomach content analysis of minke whales Balaenoptera acutorostrata from the Lofoten and Vesteralen areas, Norway |
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Q125360525 | Stream meanders increase insectivorous bird abundance in riparian deciduous forests |
Q57018527 | Strengthening forecasts of climate change impacts with multi-model ensemble averaged projections using MAGICC/SCENGEN 5.3 |
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Q58488437 | Studying spatial interactions between sympatric populations of large herbivores: a null model approach |
Q58621964 | Submersed macrophytes and grazing crayfish: an experimental study of herbivory in a California freshwater marsh |
Q113798991 | Subpopulation contributions to a breeding metapopulation of migratory arctic herbivores: survival, fecundity and asymmetric dispersal |
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Q112796954 | Summer food composition and food niche overlap of the raccoon dog, red fox and badger in Finland |
Q125590078 | Summer grazing by voles and lemmings upon subarctic snowâbed and tall herb meadow vegetation â an enclosure experiment |
Q112784579 | Supporting the restoration of complex ecosystems requires longâterm and multiâscale perspectives |
Q112800943 | Surprising roles of climate in regulating flowering phenology in a subtropical ecosystem |
Q106593186 | Survey completeness of a global citizen-science database of bird occurrence |
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Q57062567 | Synchronicity in elevation range shifts among small mammals and vegetation over the last century is stronger for omnivores |
Q115527974 | Synchronous and nonsynchronous population fluctuations of some predators and their prey in central Sweden |
Q57021024 | Synthetic datasets and community tools for the rapid testing of ecological hypotheses |
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Q110762521 | Taxonomic, functional and phylogenetic metacommunity ecology of cladoceran zooplankton along urbanization gradients |
Q58747476 | Taxonomic, functional, and phylogenetic dimensions of rodent biodiversity along an extensive tropical elevational gradient |
Q56965356 | Temperate tree expansion into adjacent boreal forest patches facilitated by warmer temperatures |
Q60297581 | Temperature and hen harrier productivity: from local mechanisms to geographical patterns |
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Q109013580 | Temperature-dependent mutational robustness can explain faster molecular evolution at warm temperatures, affecting speciation rate and global patterns of species diversity |
Q112801006 | Temperatureâmediated changes in zooplankton body size: large scale temporal and spatial analysis |
Q57122901 | Temporal and spatial differentiation in seedling emergence may promote species coexistence in Mediterranean fire-prone ecosystems |
Q111172415 | Temporal partitioning of activity: rising and falling topâpredator abundance triggers communityâwide shifts in diel activity |
Q109351268 | Temporal patch occupancy dynamics of the Siberian flying squirrel in a boreal forest landscape |
Q60541092 | Temporal scaling in analysis of animal activity |
Q115226556 | Temporal trends in the spatial bias of species occurrence records |
Q122987583 | Terrestrial gastropod diversity in an alpine region: disentangling effects of elevation, area, geometric constraints, habitat type and land-use intensity |
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Q114930332 | Testing the assumption of environmental equilibrium in an invasive plant species over a 130 year history |
Q112800928 | Testing the causes of richness patterns in the paleotropics: time and diversification in cycads (Cycadaceae) |
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Q112800994 | Testing whether ensemble modelling is advantageous for maximising predictive performance of species distribution models |
Q112801013 | Textâanalysis reveals taxonomic and geographic disparities in animal pollination literature |
Q125865257 | The African rainforest: odd man out or megafaunal landscape? African and Amazonian forests compared |
Q57996328 | The Great American Biotic Interchange revisited |
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Q57044534 | The North Atlantic Oscillation synchronises fruit production in western European forests |
Q112800939 | The ODMAP protocol: a new tool for standardized reporting that could revolutionize species distribution modeling |
Q60325278 | The Yucatan peninsula: biogeographical history 65 million years in the making |
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Q111263763 | The alternation of mutualistic ant species affects the population growth of their trophobiont mealyhug |
Q115434695 | The assembly of local communities: plants and birds in non-reclaimed mining sites |
Q112796922 | The assembly of tropical tree communities - the advances and shortcomings of phylogenetic and functional trait analyses |
Q58990169 | The attraction of the known: the importance of spatial familiarity in habitat selection in wapitiCervus elaphus |
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Q118114443 | The biogeography of parasitism in sticklebacks: distance, habitat differences and the similarity in parasite occurrence and abundance |
Q120016274 | The bog climax hypothesis: fossil arthropod and stratigraphic evidence in peat sections from southeast Alaska, USA |
Q57230303 | The breeding productivity of dark-bellied brent geese and curlew sandpipers in relation to changes in the numbers of arctic foxes and lemmings on the Taimyr Peninsula, Siberia - |
Q125558937 | The canopy arthropods of old and mature pine Pinus sylvestris in Norway |
Q120016346 | The carabid communities on peat and upland grasslands in northern England |
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Q56341083 | The community ecology of invasive species: where are we and what's next? |
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Q57068721 | The distance decay of similarity in ecological communities |
Q112798861 | The distance decay of similarity in ecological communities |
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Q125810683 | The extended phenotype of Scots pine Pinus sylvestris structures the understorey assemblage |
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Q112800986 | The ghosts of forests past and future: deforestation and botanical sampling in the Brazilian Amazon |
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Q125576492 | The impact of empirically unverified taxonomic concepts on ecological assemblage patterns across multiple spatial scales |
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Q113182428 | The impact of forest continuity and management on forest floor vegetation evaluated by species traits |
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Q112801043 | The interplay between facilitation and habitat type drives spatial vegetation patterns in global drylands |
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