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The kinetic component of KM is based on U3DSMC for interior properties and the equilibrium drifting Maxwellian at the boundary.
The KM method obtains the number density, temperature and mean velocity needed to define the equilibrium, drifting Maxwellian distribution at a boundary.
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However, we show below that the equilibrium drift load is fairly insensitive to these strict assumptions.
Finally, phenotypic complexity (and the resulting equilibrium drift load) affords a unique opportunity to contrast the action of natural selection between different organisms or different environments in a very general and unconstrained manner.
The equilibrium drift load seems to be a robust property of FGM that is determined by the number of dimensions of phenotypic space, the population size and the fitness function (especially its curvature).
However, there are two unknown parameters in the experimental system that affect the equilibrium drift load in a population: phenotypic complexity and the maximum attainable fitness that can be reached by the viruses in the laboratory environment (this parameter has been scaled to one in the previous derivations).
We utilize a model linking the equilibrium fitness (drift load) of a population to phenotypic complexity.
Although isolation by distance is generally interpreted as equilibrium between drift and migration, it may also be the consequence of serial founder effects accompanying range expansion from one or several agricultural populations [40].
This suggests that these samples are close to, or at, equilibrium between drift and gene flow.
Traditional, FST-based methods of estimating Nm make many unrealistic assumptions, among which is the equilibrium between drift and migration.
In the first part, we consider that breeds are populations in which the assumption of equilibrium between drift and mutation is verified.
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