Data from: Thermal plasticity in postembryonic life history traits of a widely distributed Collembola: Effects of macroclimate and micro

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life history traits;Folsomia quadrioculata;thermal reaction norms

DOI：

doi:10.5061/dryad.8dm60

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, 20, and 25°C) in common garden experiments. We evaluated the extent to which macroclimate could explain differences in therma

Data from: Seasonal drivers of understorey temperature buffering in temperate deciduous forests across Europe

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macroclimate;Temperature Buffering;Global warming;Canopy Density;climate change;Forest Structure and Composition;understorey;Microclimate

DOI：

doi:10.5061/dryad.cv1jg30

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experience less severe temperature extremes than suggested by currently available macroclimate data, so climate-species relationships and species’ responses

Data from: Less favorable climates constrain demographic strategies in plants

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COMPADRE Plant Matrix Database;Spatial demography;Stress-gradient hypothesis;ecological niche models;Matrix population models;Species distribution models;population dynamics;Species interactions \u2013 Abiotic stress hypothesis;climate change;Demographic compensation

DOI：

doi:10.5061/dryad.2js00

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Correlative species distribution models are based on the observed relationship between species’ occurrence and macroclimate or other

Data from: Plant community composition and species richness in the High Arctic tundra: from the present to the future

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Cassiope tetragona;Silene involucrata;Pedicularis flammea;Silene acaulis;Draba arctica;carex marítima;Stellaria longipes;Euphrasia frigida;Festuca hyperborea;Luzula nivalis;Festuca brachyphylla;plant cover;Equisetum variegatum;Arctagrostis latifolia;High Arctic tundra vegetation;Bistorta vivipara;Arenaria pseudofrigida;Sabulina stricta;boral;Arnica angustifolia;Minuartia biflora;Pedicularis hirsuta;Poa glauca;Poa arctica;Potentilla nivea;Sabulina rubella;Hierochloe alpina;Cerastium arcticum;Festuca rubra;Salix arctica;Carex bigelowii;Carex fuliginosa;Juncus castaneus;Draba glabella;Rhododendron lapponicum;Micranthes nivalis;Eriophorum triste;Kobresia myosuroides;vascular plants;Potentilla rubricaulis;Carex nardina;Papaver radicatum;Saxifraga oppositifolia;Equisetum arvense;Polemonium boreale;Potentilla hyparctica;Juncus triglumis;Saxifraga cespitosa;Carex capillaris;Oxyria digyna;Chamerion latifolium;Carex rupestris;Draba subcapitata;Alopecurus borealis;Bayesian Ordination and Regression Analysis;Kobresia simpliciuscula;Rumex acetosella;vegetation composition;Luzula confusa;Campanula uniflora;Potentilla arenosa;Saxifraga cernua;Vaccinium uliginosum;Juncus biglumis;Trisetum spicatum;Festuca vivipara;Dryas sp.

DOI：

doi:10.5061/dryad.8gr16

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ion theoretic approach to determine whether variations in species richness were best explained by macroclimate, by factors related to local topography (including

Data from: Untangling human and environmental effects on geographical gradients of mammal species richness: a global and regional evaluation

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macroclimate human accessibility human footprint macroecology terrestrial vertebrates water–energy dynamics

DOI：

doi:10.5061/dryad.qc700

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environmental conditions in explaining richness patterns. The intersection of human impacts with climate drives the geographic variation in mammal species richness

Data from: With Ellenberg indicator values towards the north: does the indicative power decrease with distance from Central Europe?

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top soil carbon and nitrogen;soil pH;Ellenberg indicator values;macroclimate gradient;forest understory vegetation;global climate change;species niche width;ecological gradient analysis;herbaceous layer

DOI：

doi:10.5061/dryad.43jj2gb

摘要：

nmental conditions, a practice further boosted by the increasing scientific focus on global change. The performance of EIV outside their geographic origin and over long gradients