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Furthermore, we explore the fate of a primordial clay-rich layer with the help of a parameterized crustal evolution model; we find that the primordial clay is locally disrupted by impacts and buried by impact-ejected material and by erupted volcanic material, but that it survives as a mostly coherent layer at depth, with limited surface exposures.
In the linear evolution model, we assumed that all mutations were mutated in a linear order shown in the left panel of Figure 2A.
Thus, the in vitro experimental evolution model we used indicates that P. falciparum can acquire after sustained artemisinin pressure the capacity to survive exposure to diverse antimalarial drugs.
To infer ancestral networks with the extended network evolution model, we need a full history of gene duplications and losses for the gene families.
On the other hand, under a mosaic evolution model we would expect divergence in patterns of evolution between whole brain size and individual brain structures, and especially among structures, as these are predicted to vary in size independently [ 1].
Using this evolution model, we developed a methodology to reconstruct a phylogeny based on rearrangement events that integrated most duplicates, and ended up with an evolutionary scenario of the mitochondrial genome in maize.
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Applying structural evolution models, we then find, with 68% confidence, that Mcore,b is less than 25 Earth masses(M⊕).
To further validate the results of landscape evolution modeling, we use a 1-D river incision model to explore the incision history of several rivers draining the Iberian Chain.
For thermal evolution models, we typically attain a subadiabatic core heat flux after a few hundred million years of evolution and prior to crystallization.
As in DNA sequence evolution models, we use a continuous time Markov chain to describe this dependency structure.
In all of the network evolution models, we started with a random connected seed graph that has 10 nodes and 25 interactions.
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