Skip to main content
Log in

Plasticity and language: an example of the Baldwin effect?

  • Published:
Philosophical Studies Aims and scope Submit manuscript

Abstract

In recent years, many scholars have suggested that the Baldwin effect may play an important role in the evolution of language. However, the Baldwin effect is a multifaceted and controversial process and the assessment of its connection with language is difficult without a formal model. This paper provides a first step in this direction. We examine a game-theoretic model of the interaction between plasticity (represented by Herrnstein reinforcement learning) and evolution in the context of a simple language game. Additionally, we describe three distinct aspects of the Baldwin effect: the Simpson–Baldwin effect, the Baldwin expediting effect and the Baldwin optimizing effect. We find that a simple model of the evolution of language lends theoretical plausibility to the existence of the Simpson–Baldwin and the Baldwin optimizing effects in this arena, but not the Baldwin expediting effect.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Notes

  1. This investigation is also useful because the learning rule we discuss here falls outside the scope of those considered in Smead and Zollman (2008).

  2. This aspect has also been explored by Mayley (1996) and genetic assimilation of acquired characters is the focus of Waddington (1953).

  3. The replicator dynamics is just one of a class of dynamics that captures this idea. The class is known as payoff-monotone dynamics.

  4. These models differ slightly from ours in that they consider so-called “act-based” learning where individuals treat each state or signal as a learning situation distinct from other states or signals. In that way individuals are not learning total contingency plans for every possible state or every possible signal, but only particular moves. Our use of Herrnstein reinforcement presumes that individuals are learning on entire contingency plans.

  5. The discrete time replicator dynamics is more conducive to simulations than the related continuous time dynamics. It should be noted, however, that there are some differences between the two dynamics which may be significant (Weibull 1997).

  6. Here, it is not specified how the trait becomes canalized. This may be important for determining the plausibility of some particular evolutionary path, but is beyond the scope of this paper.

  7. The fact that there are only two possible behaviors in this particular examples can make the interpretation of “novelty” seem artificial. However, similar interpretations and examples could be given for much larger games with many more possible actions.

  8. In this case, a “cost” could actually be beneficial, if deviations somehow resulted in higher payoffs accidentally. The cost is quantified here by looking at the proportion of plays that deviate from the “normal” best-response behavior of the learners and calculating the payoff difference between the normal behavior and the cases where deviation occurs.

  9. We should expect Herrnstein reinforcement learners to take longer to play Defect regularly against cooperators than against defectors, and likewise longer against other reinforcement learners than defectors. Hence, the “error rate” of reinforcement learners is dependent on the strategy being used by the co-player, and thus this example is not subject to the theorems regarding endogenous cost in Smead and Zollman (2008).

  10. This average payoff was determined by running 10,000 independent runs of Herrnstein reinforcement against each pure type and constructing an expanded game using these estimated payoffs.

  11. For instance, in his (1991) he says, “If it weren’t for the plasticity, however, the effect wouldn’t be there” (p. 186). But in his (1995) he weakens this claim, “... their species will evolve faster because of its greater capacity to discover design improvements in the neighborhood” (p. 79, emphasis in original).

  12. Suzuki and Arita (2004) are an exception. They consider strategies in a repeated Prisoner’s Dilemma which include plasticity. Although they do not single it out, they observe a Baldwin optimizing effect in their model as well.

  13. Our informal analysis of novelty presented above does not answer the question here, since we would need to measure directly the convergence speed in different models. This is beyond the ability of the replicator or replicator-mutator dynamics, and would instead require a finite population model. Models such as the Moran process (Moran 1962) might be appropriate for this task. Such a model would conform to our informal discussion of novelty, but space prevents us from discussing it here.

References

  • Ancel, L. W. (1999). A quantitative model of the Simpson-Baldwin effect. Journal of Theoretical Biology, 196, 197–209.

    Article  Google Scholar 

  • Ancel, L. W. (2000). Undermining the Baldwin expediting effect: Does phenotypuic plasticity accelerate evolution? Theoretical Population Biology, 58, 307–319.

    Article  Google Scholar 

  • Argiento, R., Pemantle, R., Skyrms, B., & Volkov S. (2009). Learning to signal: Analysis of a micro-level reinforcement model. Stochastic Processes and their Applications, 119(2), 373–390.

    Article  Google Scholar 

  • Barrett, J. A. (2006). Numerical simulations of the Lewis signaling game: Learning strategies, pooling equilibria, and the evolution of grammar. Technical Report MBS 06-09, University of California, Irvine Institute for Mathematical Behavioral Sciences.

  • Barrett, J. A. (2008). Dynamic partitioning and the conventionality of kinds. Philosophy of Science, 74, 527–546.

    Article  Google Scholar 

  • Deacon, T. W. (1997). The symbolic species: The co-evolution of language and the brain. New York: Norton.

    Google Scholar 

  • Dennett, D. (1991). Consciousness explained. Boston, MA: Little, Brown, and Company.

    Google Scholar 

  • Dennett, D. (1995). Darwin’s dangerous idea: Evolution and the meanings of life. New York: Simon and Shuster.

    Google Scholar 

  • Dor, D., & Jablonka, E. (2000). From cultural selection to genetic selection: A framework for the evolution of language. Selection, 1(1–3), 33–56.

    Article  Google Scholar 

  • Godfrey-Smith, P. (2003). Between Baldwin skepticisim and Baldwin boosterism. In B. H. Weber & D. J. Depew (Eds.), Evolution and learning: The Baldwin effect reconsidered. Cambridge, MA: MIT Press.

    Google Scholar 

  • Herrnstein, R. J. (1970). On the law of effect. Journal of the Experimental Analysis of Behavior, 15, 245–266.

    Google Scholar 

  • Hinton, G. E., & Nowlan, S. J. (1987). How learning can guide evolution. Complex Systems, 1, 495–502.

    Google Scholar 

  • Huttegger, S. (2007). Evolution and explanation of meaning. Philosophy of Science, 74(1), 1–27.

    Article  Google Scholar 

  • Huttegger, S. M., Skyrms, B., Smead, R., & Zollman, K. J. S. (2009). Evolutionary dynamics of lewis signaling games: Signaling systems vs. partial pooling. Synthese. doi:10.1007/s11229-009-9477-0.

  • Huttegger, S., & Zollman, K. J. (2009). Signaling games: The dynamics of evolution and learning. In A. Benz (Ed.), Language, games, and evolution, Forthcoming.

  • Lewis, D. (1969). Convention: A philosophical study. Cambridge: Harvard University Press.

    Google Scholar 

  • Mayley, G. (1996). Landscapes, learning costs, and genetic assimilation. Evolutionary Computation, 4, 213-234.

    Article  Google Scholar 

  • Mills, R., & Watson, R. (2006). On crossing fitness valleys with the Baldwin effect. In Proceedings of the tenth international conference on the simulation and synthesis of living systems, Cambridge, MA (pp. 493–499).

  • Moran, P. (1962). The stastical process of evolutionary theory. Oxford: Clarendon Press.

    Google Scholar 

  • Pawlowitsch, C. (2008). Why evolution does not always lead to an optimal signaling system. Games and Economic Behavior, 63, 203–226.

    Article  Google Scholar 

  • Pinker, S. (2000). The Language Instinct. New York: HarperCollins.

    Google Scholar 

  • Simpson, G. G. (1953). The Baldwin effect. Evolution, 7(2), 110–117.

    Article  Google Scholar 

  • Skyrms, B. (1996). Evolution of the social contract. Cambridge: Cambridge University Press.

    Google Scholar 

  • Skyrms, B. (2008). Signals: evolution, learning, and the flow of information (book manuscript).

  • Smead, R., & Zollman, K. (2008). The stability of strategic plasticity. Carnegie Mellon University, Department of Philosophy, Technical Report # CMU-PHIL-182.

  • Suzuki, R., & Arita, T. (2004). Interactions between learning and evolution: The outstanding strategy generated by the Baldwin effect. Bio Systems, 77, 57–71.

    Google Scholar 

  • Taylor, P., & Jonker, L. (1978). Evolutionarily stable strategies and game dynamics. Mathematical Biosciences, 40, 145–156.

    Article  Google Scholar 

  • Waddington, C. H. (1953). Genetic assimilation of an acquired character. Evolution, 7(2), 213–234.

    Article  Google Scholar 

  • Weibull, J. (1997). Evolutionary game theory. Cambridge: Cambridge University Press.

  • Zollman, K. J. (2005). Talking to neighbors: The evolution of regional meaning. Philosophy of Science, 72, 69–85.

    Article  Google Scholar 

Download references

Acknowledgements

The authors would like to thank Brian Skyrms, Bill Harms, Kyle Stanford, Brad Armendt, and Santiago Amaya for helpful suggestions.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kevin J. S. Zollman.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Zollman, K.J.S., Smead, R. Plasticity and language: an example of the Baldwin effect?. Philos Stud 147, 7–21 (2010). https://doi.org/10.1007/s11098-009-9447-x

Download citation

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s11098-009-9447-x

Keywords

Navigation