Teleosemantics asserts that mental content is determined by natural selection. The thesis is that content is fixed by the historical conditions under which certain cognitive mechanisms—those that produce and those that interpret representational states—were selectively successful. Content is fixed by conditions of selective success. The thesis of this paper is that teleosemantics is mistaken, that content cannot be fixed by conditions of selective success, because those conditions typically outnumber the intentional objects within a given representational state. To defend against this (...) excess, advocates of teleosemantics must attempt to privilege some conditions of success while ignoring others. This results in selective explanations that are ad hoc, thereby depriving teleosemantics of the virtues it hoped to inherit from the theory of evolution by natural selection, including its alleged naturalistic credentials. (shrink)

What is the relation between a reason and an action when the reason explains the action by giving the agent's reason for doing what he did? We may call such explanations rationalizations, and say that the reason rationalizes the action. In this paper I want to defend the ancient - and common-sense - position that rationalization is a species of ordinary causal explanation. The defense no doubt requires some redeployment, but not more or less complete abandonment of the position, as (...) urged by many recent writers. (shrink)

In this paper I defend an etiological theory of biological functions (according to which the proper function of a trait is the effect for which it was selected by natural selection) against three objections which have been influential. I argue, contrary to Millikan, that it is wrong to base our defense of the theory on a rejection of conceptual analysis, for conceptual analysis does have an important role in philosophy of science. I also argue that biology requires a normative notion (...) of a "proper function", and that a normative notion is not ahistorical. (shrink)

Biological functions are dispositions or effects a trait has which explain the recent maintenance of the trait under natural selection. This is the "modern history" approach to functions. The approach is historical because to ascribe a function is to make a claim about the past, but the relevant past is the recent past; modern history rather than ancient.

According to historical theories of biological function, a trait's function is determined by natural selection in the past. I argue that, in addition to historical functions, ahistorical functions ought to be recognized. I propose a theory of biological function which accommodates both. The function of a trait is the way it contributes to fitness and fitness can only be determined relative to a selective regime. Therefore, the function of a trait can only be specified relative to a selective regime. Apart (...) from its desirable pluralism, only this view of relational function can support the function/accident and function/malfunction distinctions commonly thought to be part of the concept of function. Furthermore, only relational function correctly characterizes the explanatory consequences of function attributions in evolutionary biology. (shrink)

The thesis that natural selection explains the frequencies of traits in populations, but not why individual organisms have the traits tehy do, is here defended and elaborated. A general concept of ‘distributive explanation’ is discussed.

I argue that our experience of expressive properties (such as the joyfulness or sadness of a piece of music) essentially involves the sensuous imagination (through simulation) of an emotion-guided process which would result in the production of the properties which constitute the realisation of the expressive properties experienced. I compare this proposal with arousal theories, Wollheim’s Freudian account, and other more closely related theories appealing to imagination such as Kendall Walton’s. I explain why the proposal is most naturally developed in (...) terms of simulation and briefly comment upon the impact of work on cross-cultural perception of facial expression, modularity and autism for the proposal. (shrink)

We examine two approaches to functions: etiological and forward-looking. In the context of functions, we raise the question, familiar to philosophers of mind, about the explanatory role of properties that are not supervenient on the mere dispositional features of a system. We first argue that the question has no easy answer in either of the two approaches. We then draw a parallel between functions and goal directedness. We conclude by proposing an answer to the question: The explanatory importance of nonsupervenient (...) properties (like having the function of doing something, or like being goal-directed) does not lie in any special causal mechanism through which these properties bring about their effects; it lies rather in the different classification of the explananda types that these properties generate. (shrink)

Melnyk complains that my account of the way reasons explain behaviour cannot be extended to cover novel behaviours. I admit that I did not extend it, but deny that it is not extendible. This, indeed, is what Chapter 6 of Dretske (1988) was all about. Noordhof finds faults with my account and claims there is another account (partial supervenience) that does a better job. I acknowledge one of the defects—a defect I was aware of when I wrote the book‐but deny (...) that the partial supervenience of content on intrinsic properties represents a better theory of the explanatory role of content. (shrink)

In this lucid portrayal of human behavior, Fred Dretske provides an original account of the way reasons function in the causal explanation of behavior.

" Biosemantics " was the title of a paper on mental representation originally printed in The Journal of Philosophy in 1989. It contained a much abbreviated version of the work on mental representation in Language Thought and Other Biological Categories. There I had presented a naturalist theory of intentional signs generally, including linguistic representations, graphs, charts and diagrams, road sign symbols, animal communications, the "chemical signals" that regulate the function of glands, and so forth. But the term " biosemantics " (...) has usually been applied only to the theory of mental representation. Let me first characterize a more general class of theories called "teleological theories of mental content" of which biosemantics is an example. Then I will discuss the details that distinguish biosemantics from other naturalistic teleological theories. (shrink)