(Journal of Philosophy, 1988, 85:303-318).

Understanding Scientific Reasoning, Fifth Edition, develops critical reasoning skills and guides students in the improvement of their scientific and technological literacy. The authors teach students how to understand and critically evaluate the scientific information they encounter in both textbooks and the popular media. With its focus on scientific pedagogy, Understanding Scientific Reasoning helps students learn how to examine scientific reports with a reasonable degree of sophistication. The book also explains how to reason through case studies using the same informal logic (...) skills employed by scientists and to analyse a complex series of propositions and hypotheses using sound scientific reasoning--Publisher's blurb. (shrink)

The Nature of Selection is a straightforward, self-contained introduction to philosophical and biological problems in evolutionary theory. It presents a powerful analysis of the evolutionary concepts of natural selection, fitness, and adaptation and clarifies controversial issues concerning altruism, group selection, and the idea that organisms are survival machines built for the good of the genes that inhabit them. "Sober's is the answering philosophical voice, the voice of a first-rate philosopher and a knowledgeable student of contemporary evolutionary theory. His book merits (...) broad attention among both communities. It should also inspire others to continue the conversation."-Philip Kitcher, Nature "Elliott Sober has made extraordinarily important contributions to our understanding of biological problems in evolutionary biology and causality. The Nature of Selection is a major contribution to understanding epistemological problems in evolutionary theory. I predict that it will have a long lasting place in the literature."-Richard C. Lewontin. (shrink)

In a recent article (Sober 1982), I criticized an account of causation proposed by Giere (1979, 1980) by describing a series of examples concerning natural selection. Collier (1983) has criticized my criticisms, saying that I misapplied Giere's proposal and misconstrued the biology. More recently, Giere (1984) has defended his theory against my criticisms. Here I argue that my criticisms still stand.

It is possible for a causal factor to raise the probability of a second factor in some situations while lowering the probability of the second factor in other situations. Must a genuine cause always raise the probability of a genuine effect of it? When it does not always do so, an "interaction" with some third factor may be the reason. I discuss causal interaction from the perspectives of Giere's counterfactual characterization of probabilistic causal connection (1979, 1980) and the "contextual unanimity" (...) model developed by, among others, Cartwright (1979) and Skyrms (1980). I argue that the contextual unanimity theory must exercise care, in a new way that seems to have gone unnoticed, in order to adequately accommodate the phenomenon, and that the counterfactual theory must be substantially revised; although it will still, pending clarification of a second kind of revision, be unable to accommodate a kind of interaction exemplified in cases like those described by Sober (1982). (shrink)

Ronald Giere's analysis of causal effectiveness in populations involves the comparison of two hypothetical populations, one in which every individual has the suspected causal factor, and the other in which none do. Elliott Sober has argued that in cases where causal effectiveness depends on relative population sizes, Giere's analysis breaks down. I take issue with this claim, and argue to the contrary that Giere's analysis can help provide insight into these cases.

La autora presenta algunas criticas generales al proyecto de reducir las leyes causales a probabilidades. Además, muestra que las leyes causales son imprescindibles para poder diferenciar las strategias efectivas de las que no lo son y da un criterio para considerar cuando podemos deducir causalidad a través de datos estadísticos.

The purpose of this essay is to investigate the properties of singular causal systems and their population manifestations, with special concern for the thesis of methodological individualism, which claims that there are no properties of social groups that cannot be adequately explained exclusively by reference to properties of individual members of those groups, i.e., at the level of individuals. Individuals, however, may be viewed as singular causal systems, i.e., as instantiations of (arrangements of) dispositional properties. From this perspective, methodological individualism (...) appears to be an ambiguous thesis: some properties of collections of (independent) systems of the same kind are reducible, but other properties of collections of (dependent) systems of the same kind are not. In cases of the first kind, therefore, methodological individualism is true, but trivial; while in cases of the second kind, it is significant, but false. Hence, if the arguments that follow are correct, at least some of the properties of social groups should qualify as emergent. (shrink)

After briefly presenting Ronald Giere's (1979, 1980) recent counterfactual characterization of population-level causation, I present two counterexamples to the characterization. The difficulty discussed stems from nonaccidental correlations that can obtain between causally effective and causally neutral factors.

After clarifying the probabilistic conception of causality suggested by Good (1961-2), Suppes (1970), Cartwright (1979), and Skyrms (1980), we prove a sufficient condition for transitivity of causal chains. The bearing of these considerations on the units of selection problem in evolutionary theory and on the Newcomb paradox in decision theory is then discussed.

In what follows, I propose to evaluate Giere's analysis by applying it to a causal process considered in evolutionary theory, namely, natural selection. To say that there is selection for a given trait is to say that possessing that trait causes differential reproductive success. If there is selection for a trait and if no other evolutionary forces impinge and there is no "sampling error" due to random drift, individuals with the trait will on average have more offspring than individuals without (...) it. But sampling error can't be discounted for finite populations; so the combined effect of selection and drift will be a probability distribution of numbers of offspring. In this event, selection for a trait will imply that the mean value of the distribution associated with the individuals possessing the trait exceeds the mean value for individuals without the trait. Evolutionary theory assigns a probability distribution of possible reproductive outputs to each organism and, thereby, views organisms as stochastic systems. This implies no commitment to indeterminacy at the microlevel, of course. (shrink)