2,634 research outputs found

    Survival of dominated strategies under evolutionary dynamics

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    We show that any evolutionary dynamic that satisfies three mild requirements— continuity, positive correlation, and innovation—does not eliminate strictly dominated strategies in all games. Likewise, we demonstrate that existing elimination results for evolutionary dynamics are not robust to small changes in the specifications of the dynamics

    Irrational behavior in the Brown - von Neuman - Nash dynamics

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    We present a class of games with a pure strategy being strictly dominated by an- other pure strategy such that the former survives along solutions of the Brown - von Neumann - Nash dynamics from an open set of initial conditions

    Robust permanence for interacting structured populations

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    The dynamics of interacting structured populations can be modeled by dxidt=Ai(x)xi\frac{dx_i}{dt}= A_i (x)x_i where xiRnix_i\in \R^{n_i}, x=(x1,,xk)x=(x_1,\dots,x_k), and Ai(x)A_i(x) are matrices with non-negative off-diagonal entries. These models are permanent if there exists a positive global attractor and are robustly permanent if they remain permanent following perturbations of Ai(x)A_i(x). Necessary and sufficient conditions for robust permanence are derived using dominant Lyapunov exponents λi(μ)\lambda_i(\mu) of the Ai(x)A_i(x) with respect to invariant measures μ\mu. The necessary condition requires maxiλi(μ)>0\max_i \lambda_i(\mu)>0 for all ergodic measures with support in the boundary of the non-negative cone. The sufficient condition requires that the boundary admits a Morse decomposition such that maxiλi(μ)>0\max_i \lambda_i(\mu)>0 for all invariant measures μ\mu supported by a component of the Morse decomposition. When the Morse components are Axiom A, uniquely ergodic, or support all but one population, the necessary and sufficient conditions are equivalent. Applications to spatial ecology, epidemiology, and gene networks are given

    Monotone methods for equilibrium selection under perfect foresight dynamics

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    This paper studies equilibrium selection in supermodular games based on perfect foresight dynamics. A normal form game is played repeatedly in a large society of rational agents. There are frictions: opportunities to revise actions follow independent Poisson processes. Each agent forms his belief about the future evolution of action distribution in the society to take an action that maximizes his expected discounted payo�. A perfect foresight path is de�ned to be a feasible path of the action distribution along which every agent with a revision opportunity takes a best response to this path itself. A Nash equilibrium is said to be absorbing if there exists no perfect foresight path escaping from a neighborhood of this equilibrium; a Nash equilibrium is said to be globally accessible if for each initial distribution, there exists a perfect foresight path converging to this equilibrium. By exploiting the monotone structure of the dynamics, a unique Nash equilibrium that is absorbing and globally accessible for any small degree of friction is identi�ed for certain classes of supermodular games. For games with monotone potentials, the selection of the monotone potential maximizer is obtained. Complete characterizations of absorbing equilibrium and globally accessible equilibrium are given for binary supermodular games. An example demonstrates that unanimity games may have multiple globally accessible equilibria for a small friction

    Stochastic approximations and differential inclusions II: applications

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    We apply the theoretical results on "stochastic approximations and differential inclusions" developed in Benaim, Hofbauer and Sorin (2005) to several adaptive processes used in game theory including: classical and generalized approachability, no-regret potential procedures (Hart and Mas-Colell), smooth fictitious play (Fudenberg and Levine

    The Selection Mutation Equation

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    Fisher's Fundamental Theorem of Natural Selection is extended to the selection mutation model with mutation rates epsilon_ij=epsilon_i, i.e. depending only on the target gene, by constructing a simple Lyapunov function. For other mutation rates stable limit cycles are possible. A basic tool is the description of some of the dynamical models as gradients with respect to a non-Riemann metric
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