A conceptual and numerical macroscopic model of this evolution, focusing on nitrogen compounds, is then presented.
A mathematical model of this evolution is presented as an attempt to integrate this analysis into computer simulations for improved reliability of lifetimes predictions.
Optimal foraging theory [ 3] takes into account the movements of animals searching for resources, but even in this case, models of the evolution of behavioral traits are rarely associated with complex ecological situations [but see [ 4, 5]].
This contradicts aerodynamic models of the evolution of flight, which assume that a transition from gliding to flapping would have been too mechanically awkward and unstable.
The reorientation of primatology, mentioned in 3.1 Selective appropriation, was another source of corrective pressure on male-centered models of human evolution, in this case, in a field where the subject of inquiry is projectively gendered.
It was not intended to introduce new models of microsatellite evolution in this work, except to make slight modifications where it made the models more suitable for Bayesian inference in an MCMC setting.
The development of this and other models of TFBS evolution has the potential to reveal the rate and pattern of CRE evolution similar to the development of codon-based models of protein evolution.
Models of protein evolution that take this into account outperform other, simpler, models [ 10- 13].
As a result, we adapt established continuous-time Markov models of sequence evolution to fit this task.
In this context, some models of structural evolution such as compensatory mutations [ 26] or conformational epistasis [ 27] might generate the observed evolutionary pattern.
