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Our investigation of the genetic basis of vertebrate morphological evolution has yielded the following findings.
A single-peak OU model assumes that morphological evolution has been constrained toward a single adaptive peak [ 4, 5].
The rapid radiation and convergent morphological evolution has confounded the resolution of relationships for many pheasants and partridges.
Parallel morphological evolution has been considered to be strong evidence for similar regimes of natural selection being at work in driving diversification [ 13].
A BM model assumes that morphological evolution has occurred under a random walk process in which morphological disparity accumulates approximately linearly through time.
The process of morphological evolution has long been viewed as one of a clear form-function relationship involving gradual adaptation to specific biota [ 1].
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The morphological evolution process has been investigated by scanning electron microscopy (SEM) at different time intervals in detail.
In all three cases, there is an apparent lack of correlation between the rate and amount of molecular and morphological evolution that has taken place e.g. [ 94].
Frequently, to evolve new morphological or behavioural forms evolution has had to reuse and adapt existing elements by utilizing the inherited genomic sequences in a new context-dependent manner.
Despite its multiple strengths, the gradual-morphological model of eye evolution has at least two shortcomings.
While there are many hypotheses on the potential influence of character integration on morphological evolution, these have yet to be explicitly tested.
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