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The modifications mainly include the determination of fiber effect-dependent parameters in terms of damage evolution, yield criterion, hardening/softening law and plastic potential.
Particularly at low taxonomic levels, recent divergence, rapid radiations, and conservative genome evolution yield limited sequence variation, and dense taxon sampling is often desirable.
Several recent meta-analyses of contemporary evolution yield the following picture: evolutionary rates above 0.1 haldanes are not uncommon (Hendry and Kinnison 1999; Gingerich 2009), even though the majority of rates are lower (Kinnison and Hendry 2001).
It has been well established that appropriately partitioned models of sequence evolution yield a better fit to empirical datasets than simple models [ 47- 49] and simulation experiments have shown that phylogenetic analysis with suitably partitioned models results in more accurate trees [ 50].
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Convergionists point out that evolution yields similarity as well as diversity.
Technological evolution yields a constantly changing threat landscape.
Yearly examination of this evolution yields the same conclusion.
In the first interval (0 < x < 2, dilute mixtures) the phase evolution yields two separated phases, namely fcc-C60 and Co2C60.
This evolution yields different autoignition delay scenarios as well as extinction at the different sites based on the local dissipation rates and their temporal histories.
The characteristic rate of evolution yielded by the explored models with selection is roughly constant over a large portion of the range of evolutionary divergence.
The total rate of evolution yields r = ∑ i π i ∑ j ≠ i μ ij, and the expected divergence between two neutrally evolving sequences separated by time t is given by d(t) = ∑ i π i [1− P ii (t, Q)].
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