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Biomedical subjects

József Garay

Publications and source records attributed to József Garay.

8 recordsLinked to original sources

A game-theoretic model for punctuated equilibrium: species invasion and stasis through coevolution.

A general theory of coevolution is developed that combines the ecological effects of species' densities with the evolutionary effects of changing phenotypes. Our approach also treats the evolutionary changes between coevolving species with discreet traits after the appearance of a new species. We apply this approach to habitat selection models where new species first emerge through competitive selection in an isolated habitat. This successful invasion is quickly followed by evolutionary changes in behavior when this species discovers the other habitat, leading to punctuated equilibrium as the final outcome.

Biological Evolution↗

Ideal free distributions, evolutionary games, and population dynamics in multiple-species environments.

In this article, we develop population game theory, a theory that combines the dynamics of animal behavior with population dynamics. In particular, we study interaction and distribution of two species in a two-patch environment assuming that individuals behave adaptively (i.e., they maximize Darwinian fitness). Either the two species are competing for resources or they are in a predator-prey relationship. Using some recent advances in evolutionary game theory, we extend the classical ideal free distribution (IFD) concept for single species to two interacting species. We study population dynamical consequences of two-species IFD by comparing two systems: one where individuals cannot migrate between habitats and one where migration is possible. For single species, predator-prey interactions, and competing species, we show that these two types of behavior lead to the same population equilibria and corresponding species spatial distributions, provided interspecific competition is patch independent. However, if differences between patches are such that competition is patch dependent, then our predictions strongly depend on whether animals can migrate or not. In particular, we show that when species are settled at their equilibrium population densities in both habitats in the environment where migration between habitats is blocked, then the corresponding species spatial distribution need not be an IFD. Thus, when species are given the opportunity to migrate, they will redistribute to reach an IFD (e.g., under which the two species can completely segregate), and this redistribution will also influence species population equilibrial densities. Alternatively, we also show that when two species are distributed according to the IFD, the corresponding population equilibrium can be unstable.

Animal Migration↗

When does the variance of replicator fitness decrease?

For the general replicator dynamics with regular relative advantage functions (having non-singular Jacobian and symmetrized Jacobian), it will be shown that the variance of marginal fitness of the replicators strictly decreases along each trajectory of the replicator dynamics near an interior rest point if and only if this rest point is a regular evolutionarily stable state.

Biological Evolution↗

Evolutionarily stable sets in the single-locus frequency-dependent model of natural selection.

Recent developments in the static theory of evolutionarily stable sets (ESSets) are applied to the single-locus frequency-dependent model of natural selection. Particular emphasis is paid to the ESSet properties of the preimage of an ESS (or ESSet) under the genotype-phenotype map. When an ESS is realized in genetic equilibrium with redundancy in a diploid sexual population, the basic problem in biological terms is whether the corresponding set of allele frequencies is an evolutionarily stable set. The interesting question of the dynamic stability of this preimage is also discussed and a geometric condition developed which implies its evolutionary and dynamic stability.

Alleles↗

Coincidence of ESAD and ESS in dominant-recessive hereditary systems.

The paper deals with the following question: when do the phenotypic evolutionarily stable state (ESS) and the evolutionarily stable allele distribution (ESAD) coincide? It is supposed that for a sexual population, in dominant-recessive inheritance system, n allele at one autosomal locus determine n possible pure individual phenotypes and each pure phenotype is obtained as the phenotype of a homozygote. Under these conditions, earlier results of the authors imply that, if a phenotype distribution is an ESS then the allele distribution generating it is an ESAD. In this paper, apart from a certain degenerate pay-off matrices, the inverse statement is also proved: if a distribution is an ESAD then the corresponding phenotypic distribution is an ESS.

Alleles↗

Evolutionary stability in Lotka-Volterra systems.

The Lotka-Volterra model of population ecology, which assumes all individuals in each species behave identically, is combined with the behavioral evolution model of evolutionary game theory. In the resultant monomorphic situation, conditions for the stability of the resident Lotka-Volterra system, when perturbed by a mutant phenotype in each species, are analysed. We develop an evolutionary ecology stability concept, called a monomorphic evolutionarily stable ecological equilibrium, which contains as a special case the original definition by Maynard Smith of an evolutionarily stable strategy for a single species. Heuristically, the concept asserts that the resident ecological system must be stable as well as the phenotypic evolution on the "stationary density surface". The conditions are also shown to be central to analyse stability issues in the polymorphic model that allows arbitrarily many phenotypes in each species, especially when the number of species is small. The mathematical techniques are from the theory of dynamical systems, including linearization, centre manifolds and Molchanov's Theorem.

Animals↗

Stability in N-species coevolutionary systems.

Stability criteria have recently been developed for coevolutionary Lotka-Volterra systems where individual fitness functions are assumed to be linear in the population state. We extend these criteria as part of a general theory of coevolution (that combines effects of ecology and evolution) based on arbitrary (i.e. nonlinear) fitness functions and a finite number of individual phenotypes. The central role of the stationary density surface where species' densities are at equilibrium is emphasized. In particular, for monomorphic resident systems, it is shown coevolutionary stability is equivalent to ecological stability combined with evolutionary stability on the stationary density surface. Also discussed is how our theory relates to recent treatments of phenotypic coevolution via adaptive dynamics when there is a continuum of individual phenotypes.

Biological Evolution↗

Many species partial adaptive dynamics.

A system of n asexual populations is considered in which both intra- and interspecific frequency-dependent matrix game conflicts with a lack of information are involved and the weak perturbation condition is satisfied (mutation is a very rare event and selection is quick). A new partial adaptive game dynamics is proposed that takes into account that the mutants interact not only with the residents but among themselves as well. It is also shown that if the Nash equilibrium (NE) is totally mixed and the interaction matrices are Replicator-Lyapunov stable (RL-stable), then the NE is an asymptotically stable point of these new dynamics.

Adaptation, Physiological↗