Evolution under the multilocus Levene model without epistasis
Evolution under the multilocus Levene model is investigated. The linkage map is arbitrary, but epistasis is absent. The geometric-mean fitness, \(\tilde{w}(\rho)\), depends only on the vector of gene frequencies, ho; it is nondecreasing, and the single-generation change is zero only on the set, \(\Lambda\), of gametic frequencies at gene-frequency equilibrium. The internal gene-frequency equilibria are the stationary points of \(\tilde{w}(\rho)\). If the equilibrium points \(\hat{\rho}\) of \(\rho(t)\) (where \(t\) denotes time in generations) are isolated, as is generic, then \(\rho(t)\) converges as \(t\rightarrow\infty\) to some \(\hat{\rho}\). Generically, \(\rho(t)\) converges to a local maximum of \(\tilde{w}(\rho)\). Write the vector of gametic frequencies, \(p\), as \((\rho, d)^T\), where \(d\) represents the vector of linkage disequilibria. If \(\hat{\rho}\) is a local maximum of \(\tilde{w}(\rho)\), then the equilibrium point \((\hat{\rho}, 0)^T\) is asymptotically stable. If either there are only two loci or there is no dominance, then \(d(t)\rightarrow 0\) globally as \(t\rightarrow\infty\). In the second case, \(\tilde{w}(\rho)\) has a unique maximum \(\hat{\rho}\) and \((\hat{\rho}, 0)^T\) source is globally asymptotically stable. If underdominance and overdominance are excluded, and if at each locus, the degree of dominance is deme independent for every pair of alleles, then the following results also hold. There exists exactly one stable gene-frequency equilibrium (point or manifold), and it is globally attracting. If an internal gene-frequency equilibrium exists, it is globally asymptotically stable. On \(\Lambda\), (i) the number of demes, \(\Gamma\), is a generic upper bound on the number of alleles present per locus; and (ii) if every locus is diallelic, generically at most \(\Gamma -1\) loci can segregate. Finally, if migration and selection are completely arbitrary except that the latter is uniform (i.e., deme independent), then every uniform selection equilibrium is a migration-selection equilibrium and generically has the same stability as under pure selection.
- Evolution and polymorphism in the multilocus Levene model with no or weak epistasis
- Evolution and polymorphism in the multilocus Levene model with no or weak epistasis
- Evolution under the multiallelic Levene model
- Polymorphism in multiallelic migration-selection models with dominance
- Multilocus selection in subdivided populations. I: Convergence properties for weak or strong migration
- A Hopf bifurcation theorem for difference equations approximating a differential equation
- Convergence of multilocus systems under weak epistasis or weak selection
- Convergence to equilibrium in a polylocus polyallele population with additive selection
- Convergence to equilibrium of the two locus additive viability model
- Cycling in simple genetic systems
- Epistatic selection in a multi-locus Levene model and implications for linkage disequilibrium
- Evolution at a multiallelic locus under migration and uniform selection
- Evolution under multiallelic migration-selection models
- Evolution under the multiallelic Levene model
- Global convergence properties in multilocus viability selection models: The additive model and the Hardy-Weinberg law
- Hopf bifurcation in the two locus genetic model
- scientific article; zbMATH DE number 3138903 (Why is no real title available?)
- scientific article; zbMATH DE number 3920272 (Why is no real title available?)
- scientific article; zbMATH DE number 3954716 (Why is no real title available?)
- scientific article; zbMATH DE number 4064811 (Why is no real title available?)
- scientific article; zbMATH DE number 3673925 (Why is no real title available?)
- scientific article; zbMATH DE number 3683431 (Why is no real title available?)
- scientific article; zbMATH DE number 1324227 (Why is no real title available?)
- scientific article; zbMATH DE number 1455131 (Why is no real title available?)
- scientific article; zbMATH DE number 791391 (Why is no real title available?)
- scientific article; zbMATH DE number 3249395 (Why is no real title available?)
- scientific article; zbMATH DE number 3278338 (Why is no real title available?)
- scientific article; zbMATH DE number 3286332 (Why is no real title available?)
- scientific article; zbMATH DE number 3063483 (Why is no real title available?)
- Mathematical population genetics. I: Theoretical introduction.
- Matrix Analysis
- Multilocus selection in subdivided populations II. Maintenance of polymorphism under weak or strong migration
- Multilocus selection in subdivided populations. I: Convergence properties for weak or strong migration
- Patterns of multiallelic polymorphism maintained by migration and selection.
- Polymorphism in multiallelic migration-selection models with dominance
- Polymorphism in the two-locus Levene model with nonepistatic directional selection
- Recent Advances in Liapunov Stability Theory
- Representation of nonepistatic selection models and analysis of multilocus Hardy-Weinberg equilibrium configurations
- Stable cycling in discrete-time genetic models.
- Stable linkage disequilibrium without epistasis in subdivided populations
- Subdivided populations: a review of the one- and two-locus deterministic theory
- The dynamics of migration-selection models
- The two-locus multi-allele additive viability model
- Existence of steady-state probability distributions in multilocus models for genotype evolution
- Convergence of multilocus systems under weak epistasis or weak selection
- Epistatic selection in a multi-locus Levene model and implications for linkage disequilibrium
- Finiteness of equilibria set for a nonepistatic selection under multilocus Mendel dominance
- The number of equilibria in the diallelic levene model with multiple demes
- Two-locus clines maintained by diffusion and recombination in a heterogeneous environment
- Long-term evolution of multilocus traits
- Multilocus population-genetic theory
- The effects of linkage and gene flow on local adaptation: a two-locus continent-island model
- Equilibrium properties of a multi-locus, haploid-selection, symmetric-viability model
- The consequences of gene flow for local adaptation and differentiation: a two-locus two-deme model
- Epistasis in the multiple locus symmetric viability model
- A survey of migration-selection models in population genetics
- Evolution and polymorphism in the multilocus Levene model with no or weak epistasis
- Evolution and polymorphism in the multilocus Levene model with no or weak epistasis
- Polymorphism in the two-locus Levene model with nonepistatic directional selection
- Global bifurcation and stability for semi-infinite cline
- Evolution under the multiallelic Levene model
This page was built for publication: Evolution under the multilocus Levene model without epistasis
Report a bug (only for logged in users!)Click here to report a bug for this page (MaRDI item Q615662)