Chasnov J R
Department of Mathematics, Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong.
Theor Popul Biol. 2012 Mar;81(2):119-30. doi: 10.1016/j.tpb.2011.12.004. Epub 2011 Dec 21.
Under haploid selection, a multi-locus, diallelic, two-niche Levene (1953) model is studied. Viability coefficients with symmetrically opposing directional selection in each niche are assumed, and with a further simplification that the most and least favored haplotype in each niche shares no alleles in common, and that the selection coefficients monotonically increase or decrease with the number of alleles shared. This model always admits a fully polymorphic symmetric equilibrium, which may or may not be stable. We show that a stable symmetric equilibrium can become unstable via either a supercritical or subcritical pitchfork bifurcation. In the supercritical bifurcation, the symmetric equilibrium bifurcates to a pair of stable fully polymorphic asymmetric equilibria; in the subcritical bifurcation, the symmetric equilibrium bifurcates to a pair of unstable fully polymorphic asymmetric equilibria, which then connect to either another pair of stable fully polymorphic asymmetric equilibria through saddle-node bifurcations, or to a pair of monomorphic equilibria through transcritical bifurcations. As many as three fully polymorphic stable equilibria can coexist, and jump bifurcations can occur between these equilibria when model parameters are varied. In our Levene model, increasing recombination can act to either increase or decrease the genetic diversity of a population. By generating more hybrid offspring from the mating of purebreds, recombination can act to increase genetic diversity provided the symmetric equilibrium remains stable. But by destabilizing the symmetric equilibrium, recombination can ultimately act to decrease genetic diversity.
在单倍体选择下,研究了一个多基因座、双等位基因、双生态位的莱文(1953)模型。假设每个生态位中存在对称反向定向选择的生存系数,并进一步简化为每个生态位中最受青睐和最不受青睐的单倍型没有共同的等位基因,且选择系数随着共享等位基因的数量单调增加或减少。该模型总是存在一个完全多态的对称平衡,其可能稳定也可能不稳定。我们表明,一个稳定的对称平衡可以通过超临界或亚临界叉形分岔变得不稳定。在超临界分岔中,对称平衡分岔为一对稳定的完全多态不对称平衡;在亚临界分岔中,对称平衡分岔为一对不稳定的完全多态不对称平衡,然后通过鞍结分岔连接到另一对稳定的完全多态不对称平衡,或者通过跨临界分岔连接到一对单态平衡。多达三个完全多态的稳定平衡可以共存,并且当模型参数变化时,这些平衡之间可能会发生跳跃分岔。在我们的莱文模型中,增加重组可以增加或减少种群的遗传多样性。通过纯种交配产生更多的杂交后代,只要对称平衡保持稳定,重组就可以增加遗传多样性。但通过破坏对称平衡,重组最终可以减少遗传多样性。