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According to the insurance hypothesis, species richness can buffer against spatiotemporal disturbances, thereby insuring functioning in changing environments.
We found no support for the Ecomorph Convergence hypothesis; species using the same structural habitat were no more similar in dewlap configuration than expected by chance.
In keeping with this hypothesis, species of birds and mammals with larger brain masses relative to body mass tend to have been more successful at establishing viable populations in novel environments [18], [20].
(i) According to the generation time hypothesis, species with shorter generation times are expected to have higher substitution rates because their genomes are copied more often per time unit [ 109].
According to the range position hypothesis, species are expected to inhabit increasingly fewer localities when moving along a gradient from the centre of the species' geographical distribution range toward the edges of the range [ 2, 31, 32].
Under this hypothesis, species within communities are constrained by environmental factors; the overall species abundance within a community is driven to a trait average optimal for the specific environment.
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We reject the hypothesis that species distributions along a ridge-valley catena at Korup are caused by species differences in trees ≥1 cm dbh.
This confirms the hypothesis that species from one group should lead to similar models when trained against species from a different group.
Species richness was the first biodiversity component to be related to ecosystem functioning [21] supporting the hypothesis that species complementarity and sampling effects both enhance resource use and productivity.
Darwin's theory of evolution cites plenty of scientific evidence to support the hypothesis that species evolve to fit their environments.
Some ecologists also note that the intermediate disturbance hypothesis overemphasizes species diversity as a measure of recovery from a disturbance.
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