Works matching IS 02698463 AND DT 2022 AND VI 36 AND IP 1
Results: 22
Fine‐scale spatial patterns of wildlife disease are common and understudied.
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- Functional Ecology, 2022, v. 36, n. 1, p. 214, doi. 10.1111/1365-2435.13942
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Plant litter influences the temporal stability of plant community biomass in an alpine meadow by altering the stability and asynchrony of plant functional groups.
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- Functional Ecology, 2022, v. 36, n. 1, p. 148, doi. 10.1111/1365-2435.13935
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Weak interactions between strong interactors in an old‐field ecosystem: Control of nitrogen cycling by coupled herbivores and detritivores.
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- Functional Ecology, 2022, v. 36, n. 1, p. 133, doi. 10.1111/1365-2435.13932
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Ecological mechanisms underlying aridity thresholds in global drylands.
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- Functional Ecology, 2022, v. 36, n. 1, p. 4, doi. 10.1111/1365-2435.13962
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Cracks in the mirror hypothesis: High specularity does not reduce detection or predation risk.
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- Functional Ecology, 2022, v. 36, n. 1, p. 239, doi. 10.1111/1365-2435.13963
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Biogeographical distributions of nitrogen‐cycling functional genes in a subtropical estuary.
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- Functional Ecology, 2022, v. 36, n. 1, p. 187, doi. 10.1111/1365-2435.13949
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Nutrient cycling and self‐regulation determine food web stability.
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- Functional Ecology, 2022, v. 36, n. 1, p. 202, doi. 10.1111/1365-2435.13961
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Central and Northern European caterpillar assemblages show strong phylogenetic structure.
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- Functional Ecology, 2022, v. 36, n. 1, p. 262, doi. 10.1111/1365-2435.13956
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The mating system affects the temperature sensitivity of male and female fertility.
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- Functional Ecology, 2022, v. 36, n. 1, p. 92, doi. 10.1111/1365-2435.13952
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Opportunities, challenges and pitfalls in characterizing plant water‐use strategies.
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- Functional Ecology, 2022, v. 36, n. 1, p. 24, doi. 10.1111/1365-2435.13945
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Biophysical models unravel associations between glucocorticoids and thermoregulatory costs across avian species.
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- Functional Ecology, 2022, v. 36, n. 1, p. 64, doi. 10.1111/1365-2435.13946
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Feather corticosterone reveals developmental challenges in a long‐term study of juvenile northern spotted owls.
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- Functional Ecology, 2022, v. 36, n. 1, p. 51, doi. 10.1111/1365-2435.13944
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Experimental evidence of rapid heritable adaptation in the absence of initial standing genetic variation.
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- Functional Ecology, 2022, v. 36, n. 1, p. 226, doi. 10.1111/1365-2435.13943
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Nongenetic inheritance of behavioural variability is context specific and sex specific.
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- Functional Ecology, 2022, v. 36, n. 1, p. 83, doi. 10.1111/1365-2435.13931
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Distinguishing between unreliability and dishonesty: A comparative study of aggressive communication in crayfish.
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- Functional Ecology, 2022, v. 36, n. 1, p. 73, doi. 10.1111/1365-2435.13927
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Experimentally decomposing phytoplankton community change into ecological and evolutionary contributions.
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- Functional Ecology, 2022, v. 36, n. 1, p. 120, doi. 10.1111/1365-2435.13923
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Positive heterospecific interactions can increase long‐term diversity of plant communities more than negative conspecific interactions alone.
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- Functional Ecology, 2022, v. 36, n. 1, p. 159, doi. 10.1111/1365-2435.13941
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Variation in plant carbon, nitrogen and phosphorus contents across the drylands of China.
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- Functional Ecology, 2022, v. 36, n. 1, p. 174, doi. 10.1111/1365-2435.13937
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Caves, crevices and cooling capacity: Roost microclimate predicts heat tolerance in bats.
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- Functional Ecology, 2022, v. 36, n. 1, p. 38, doi. 10.1111/1365-2435.13918
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Interactions between silicon and alkaloid defences in endophyte‐infected grasses and the consequences for a folivore.
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- Functional Ecology, 2022, v. 36, n. 1, p. 249, doi. 10.1111/1365-2435.13916
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Growth responses of ectomycorrhizal and arbuscular mycorrhizal seedlings to low soil nitrogen availability in a tropical montane forest.
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- Functional Ecology, 2022, v. 36, n. 1, p. 107, doi. 10.1111/1365-2435.13901
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Cover Picture and Issue Information.
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- Functional Ecology, 2022, v. 36, n. 1, p. 1, doi. 10.1111/1365-2435.13834
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- Article