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The interpretation was that Hsp90 is a capacitor of morphological evolution: It buffers a preexisting genetic variation that is not expressed and accumulates under neutral conditions; its inhibition will induce the expression of this variation.
To make full use of the wing as a model of the cellular and genetic basis of morphological evolution, it will be necessary to also study larger differences in wing size and shape.
When viewed from the perspective of morphological evolution, it is now evident that taxa presently defined as Cerapachys are grouped together not due to unique common descent, but rather because collectively they retain a similar, generalized morphology.
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The presence of weak interconnection between traits parcelled into different modules has been hypothesized to facilitate morphological evolution because it mitigates the widespread effect of constraints in a system and allows modules to vary independently (e.g., [ 10- 12]).
This study suggests that, while the total number of significant results is relatively limited, high integration constrains morphological evolution more often than it facilitates it.
Furthermore, the Lausche Volcano provides valuable information concerning the morphological evolution of its broader environs.
The proponents of the punctuated equilibrium model propose not only that morphological evolution is jerky but also that it is associated with speciation events.
As expected under the ecological theory of adaptive radiation [ 4], it increased diversification as well as rates of morphological evolution.
It is the implausibility of this scenario that we regard convergent morphological evolution as a more likely explanation.
It is important to note that the relationship between morphological integration and morphological evolution are poorly understood [10].
Similar morphologies must have evolved several times independently, but details on this morphological evolution are scarce.
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