We extend previous work by modeling evolution of communication using a spatialized genetic algorithm which recombines strategies purely locally.Here cellular automata are used as a spatialized environment in which individuals gain points by feeding from drifting food sources and are 'harmed' if they fail to hide from migrating predators. Our individuals are capable of making one of two arbitrary sounds, heard only locally by their immediate neighbors. They can respond to sounds from their neighbors by opening their mouths or by hiding. By opening their mouths in the presence of food they maximize gains; by hiding when a predator is present they minimize losses. We consider the result a 'natural' template for benefits from communication; unlike a range of other studies, it is here only the recipient of communicated information that immediately benefits.A community of'perfect communicators' could be expected to make a particular sound when successfully feeding, responding to that same sound from their neighbors by opening their mouths. They could be expected to make a different sound when 'hurt' and respond to that second sound from their neighbors by hiding.Suppose one starts from a small set of 'Adam and Eve' strategies randomized across a cellular automata array, and uses a genetic algorithm which operates purely locally by cross-breeding strategies with their most successful neighbors. Can one, in such an environment, expect evolution of local communities of 'perfect communicators'? With some important qualifications, the answer is 'yes'.

We extend previous work on cooperation to some related questions regarding the evolution of simple forms of communication. The evolution of cooperation within the iterated Prisoner's Dilemma has been shown to follow different patterns, with significantly different outcomes, depending on whether the features of the model are classically perfect or stochastically imperfect (

What is it for a sound or gesture to have a meaning, and how does it come to have one? In this paper, a range of simulations are used to extend the tradition of theories of meaning as use. The authors work throughout with large spatialized arrays of sessile individuals in an environment of wandering food sources and predators. Individuals gain points by feeding and lose points when they are hit by a predator and are not hiding. They can also make sounds heard by immediate neighbours in the array, and can respond to sounds from immediate neighbours. No inherent meaning for these sounds is built into the simulation; under what circumstances they are sent, if any, and what the response to them is, if any, vary initially with the strategies randomized across the array. These sounds do take on a specific function for communities of individuals, however, with any of three forms of strategy change: direct imitation of strategies of successful neighbours, a localized genetic algorithm in which strategies are 'crossed' with those of successful neighbours, and neural net training on the behaviour of successful neighbours. Starting from an array randomized across a large number of strategies, and using any of these modes of strategy change, communities of 'communicators' emerge. Within these evolving communities the sounds heard from immediate neighbours, initially arbitrary across the array, come to be used for very specific communicative functions. 'Communicators' make a particular sound on feeding and respond to that same sound from neighbours by opening their mouths; they make a different sound when hit with a predator and respond to that sound by hiding. Robustly and persistently, even in simple computer models of communities of self-interested agents, something suggestively like signalling emerges and spreads.

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We work with a large spatialized array of individuals in an environment of drifting food sources and predators. The behavior of each individual is generated by its simple neural net; individuals are capable of making one of two sounds and are capable of responding to sounds from their immediate neighbors by opening their mouths or hiding. An individual whose mouth is open in the presence of food is "fed" and gains points; an individual who fails to hide when a predator is present is "hurt" by losing points. Opening mouths, hiding, and making sounds each exact an energy cost. There is no direct evolutionary gain for acts of cooperation or "successful communication" per se.In such an environment we start with a spatialized array of neural nets with randomized weights. Using standard learning algorithms, our individuals "train up" on the behavior of successful neighbors at regular intervals. Given that simple setup, will a community of neural nets evolve a simple language for signaling the presence of food and predators? With important qualifications, the answer is "yes." In a simple spatial environment, pursuing individualistic gains and using partial training on successful neighbors, randomized neural nets can learn to communicate.