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Land plant ecology on the basis of functional traits would thus suggest that plants adapt their biomechanical structure [19], [20]; this hypothesis was to be addressed in the current study with respect to the structure of cellulose.
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When coevolving traits do not affect other functions, coevolution and evolution of functional traits may be orthogonal and proceed independently.
But at least some of functional traits of these technologies affect fitness.
Where the temporal distribution of functional traits is more often multimodal, it can also be unimodal, mimicking that of a stylistic trait.
The interaction of functional traits with habitat availability also significantly explained parasitoid ASRs.
Differences in these relationships would suggest changes in the relative importance of functional traits among sites.
Here we show that predator removal may also drive the evolution of functional traits in prey.
The 99th-percentile dispersal distances of the alien species ranged from 3.8 m to 309.3 m, and these distances were longer than the values predicted on the basis of their functional traits, such as terminal velocity.
For this purpose, the trait-based approach has promoted the analysis of functional trait distributions within communities.
Many researchers interested in the effects of biodiversity on ecosystems focus on aspects of functional diversity including functional group richness (numbers of functional groups), functional composition (combinations of functional groups) and continuous measures of functional trait diversity [36], [37].
The advantage of using functional traits instead of taxonomic composition (an entirely structural approach) of communities is bound to the a priori predictable response of traits to individual stressors, because each selection pressure affects different traits.
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