Elliott Sober

It is a challenge to explain how evolutionary altruism can evolve by the process of natural selection, since altruists in a group will be less fit than the selfish individuals in the same group who receive benefits but do not make donations of their own. Darwin proposed a theory of group selection to solve this puzzle. Very simply, even though altruists are less fit than selfish individuals within any single group, groups of altruists are more fit than groups of selfish individuals. If a population is subdivided into many groups that vary in their altruistic tendencies, altruism will be favored at the level of selection among groups even as it is being disfavored at the level of selection among individuals within groups. Darwin’s scenario became the basis for a theoretical framework called multilevel selection theory.

In ‘Two Dogmas of Empiricism’, Quine attacks the analytic/synthetic distinction and defends a doctrine that I call epistemological holism. Now, almost fifty years after the article’s appearance, what are we to make of these ideas? I suggest that the philosophical naturalism that Quine did so much to promote should lead us to reject Quine’s brief against the analytic/synthetic distinction; I also argue that Quine misunderstood Carnap's views on analyticity. As for epistemological holism, I claim that this thesis does not follow from the logical point that Duhem and Quine made about the role of auxiliary assumptions in hypothesis testing, and that the thesis should be rejected.

Human nature is intriguing in such that it can express both negative and positive emotions, as in kindness and cruelty. The question is whether both are a natural part of our nature as human beings, or is one produced to serve as the alternate of the other. Another question that is brought to the table in this chapter is how does one determine what is natural and what is not, being its true definition? The chapter attempts to answer these questions based on evolution theory, whether events earlier in history served as a promoter for the emotions of today. Was the nature of kindness and caring inherent in a human being at the beginning of time, or is it only through the changes and events over time that it has developed? The chapter aims to aid the reader in understanding our human tendencies.

Solipsism poses a familiar epistemological problem. Each of us has beliefs about a world that allegedly exists outside our own minds. The problem is to justify these nonsolipsistic convictions. One standard approach is to argue that the existence of things outside our own sensations may reasonably be inferred from regularities that obtain within our sensations. Certain experiences, which I will call tiger sounds and tiger visual images, exhibit a striking correlation. We can explain the existence of this correlation by postulating an entity that is a cause of both. If there were tigers, it would be no surprise that certain sights and certain sounds tend to co-occur. Our rejection of solipsism can thus be justified by appeal to an abductive argument; we advance an inference to the best explanation conforming to the pattern that Reichenbach called the principle of the common cause.

“Absence of evidence isn’t evidence of absence” is a slogan that is popular among scientists and nonscientists alike. This article assesses its truth by using a probabilistic tool, the Law of Likelihood. Qualitative questions (“Is E evidence about H ?”) and quantitative questions (“How much evidence does E provide about H ?”) are both considered. The article discusses the example of fossil intermediates. If finding a fossil that is phenotypically intermediate between two extant species provides evidence that those species have a common ancestor, does failing to find such a fossil constitute evidence that there was no common ancestor? Or should the failure merely be chalked up to the imperfection of the fossil record? The transitivity of the evidence relation in simple causal chains provides a broader context, which leads to discussion of the fine-tuning argument, the anthropic principle, and observation selection effects.

Evidence and Evolution has four chapters: (1) Evidence, (2) Intelligent Design, (3) Natural Selection, and (4) Common Ancestry. The first chapter develops tools that are used in the rest of the book, though more ideas about evidence are added. In Chapter 1, I endorse a pluralistic outlook—Bayesianism is fine in some inference problems, likelihoodism in others, and AIC in still others. In Chapter Two, on intelligent design, I try to develop the strongest possible formulation of the design argument for the existence of God, after which I criticize the argument so conceived. This second chapter also attempts to resuscitate the concept of testability. Chapter 3, on natural selection, discusses how to evaluate competing hypotheses on evolution mechanisms and evaluate the use of the principle of common cause, molecular data, and cladistic parsimony. Chapter 4 is on common ancestry: what it means to say that all life on earth has a common ancestor, and s. Why should the similarity of two species be evidence that they have a common ancestor? The chapter concludes with a discussion of how biologists use cladistic parsimony to infer phylogenetic trees and compare it with explicit statistical approaches.

My critical remarks' on Alexander Rosenberg’s article on fitness have elicited a rejoinder from Mary Williams and Rosenberg himself. They charge that my criticisms are a “tissue of misunderstandings” (738); since they misunderstand my own position in fundamental ways, it may help to try to clarify the points that divide us. In the interest of brevity, I will ignore technical issues concerning the internal correctness of Williams’s axiomatization and will focus on questions of broader philosophical interest.

A model of a Markov process is presented in which observing the present state of a system is asymmetrically related to inferring the system's future and inferring its past. A likelihood inference about the system's past state, based on observing its present state, is justified no matter what the parameter values in the model happen to be. In contrast, a probability inference of the system's future state, based on observing its present state, requires further information about the parameter values

When two causally independent processes each have a quantity that increases monotonically (either deterministically or in probabilistic expectation), the two quantities will be correlated, thus providing a counterexample to Reichenbach's principle of the common cause. Several philosophers have denied this, but I argue that their efforts to save the principle are unsuccessful. Still, one salvage attempt does suggest a weaker principle that avoids the initial counterexample. However, even this weakened principle is mistaken, as can be seen by exploring the concepts of homology and homoplasy used in evolutionary biology. I argue that the kernel of truth in the principle of the common cause is to be found by separating metaphysical and epistemological issues; as far as the epistemology is concerned, the Likelihood Principle is central.

Several philosophers have argued recently that semantic properties do play a causal role. 1 It is our view that none of these arguments are satisfactory. Our aim is to reveal some of the deficiencies of these arguments, and to reassess the question in our own way. In section 1, we shall explain in more detail what is involved in the pretheoretical idea of a causally efficacious property and so provide a fuller sense of the issue. In section 2 we shall discuss Fodor's and Kim's arguments that the semantic properties of mental events are causally efficacious. Their tactic is to articulate sufficient conditions for the causal efficacy of a property, and then apply these conditions to the psychological properties under consideration. We shall show that both formulations are inadequate. However, each account can remedy some of the defects of the other. We shall argue that by putting the two together, and modifying this combined account in certain ways, we can arrive at something that might just pass as a general sufficient condition for causal efficacy. We believe that the question of causal efficacy of content is best approached as a question in the philosophy of science. If one wants to know whether a given species of property is efficacious, the most productive strategy is to find a science that investigates the properties and examine the role they are assigned. In keeping with this attitude we shall restrict our discussion to the notion of content deployed within cognitive science. In section 3 we examine the role of content in cognitive science and discuss whether this role suits content to the conditions on efficacy articulated in section two. Our conclusion will be conditional and hedged: on certain views of cognitive science, content will meet the sufficient condition for efficacy. If other views are correct, the question remains open.

These essays by leading scientists and philosophers address conceptual issues that arise in the theory and practice of evolutionary biology. The third edition of this widely used anthology has been substantially revised and updated. Four new sections have been added: on women in the evolutionary process, evolutionary psychology, laws in evolutionary theory, and race as social construction or biological reality. Other sections treat fitness, units of selection, adaptationism, reductionism, essentialism, species, phylogenetic inference, cultural evolution, and evolutionary ethics. Each of the twelve sections contains two or three essays that develop different views of the subject at hand. For example, the section on evolutionary psychology offers one essay by two founders of the field and another that questions its main tenets. One sign that a discipline is growing is that there are open questions, with multiple answers still in competition; the essays in this volume demonstrate that evolutionary biology and the philosophy of evolutionary biology are living, growing disciplines.

Alexander Rosenberg began his recent article on the concept of fitness with the remark that “debates about the cognitive status of the Darwinian theory of natural selection should have ended long ago.” I agree that this obsession need to be overcome. But Rosenberg repeats some of the old mistakes and invents epicycles on others. In this comment I will not be able to circumscribe fully the range of the topics that an adequate treatment of this cluster of problems demands. A few critical comments will indicate what I find wanting in Rosenberg’s treatment.

Philosophy of mind is, and for a long while has been, 99% metaphysics and 1% epistemology. But the fundamental question cognitive ethologists face is epistemological: what count as evidence that a creature has a mind, and if the creature does have a mind, what evidence is relevant to deciding which mental state should be attributed to it? The usual answer that cognitive ethologists give is that one’s explanation should be “conservative”. It recommends a two-part plausibility ordering: mindless is preferred to minded, and first-order intentionality is preferred to second-order intentionality. I argue that the principle of conservatism is not a parsimony principle, and it doesn’t have any justification. What is needed is observational test. I also suggest a strategy for designing experiments in the future. What I offered here is a methodological version of naturalism.

I want to explore what happens to two philosophical issues when we assume that the mind, a functional device, is to be understood by the same sort of functional analysis that guides biological investigation of other organismic systems and characteristics. The first problem area concerns the concept of rationality, its connection with reliability and reproductive success, and the status of rationality hypotheses in attribution of beliefs. It has been argued that ascribing beliefs to someone requires the assumption that that person is rational. It also has been argued that evolutionary theory can account for the capacity we have for rational thought by appealing to the idea that rational methods for constructing beliefs are reliable and therefore represented a selected advantage. Both of these claims about rationality are critically examined. In the second part of the paper, I turn to some criticisms that have been advanced against "functionalist" solutions to the mind/body problem. These criticisms are defused when that doctrine is understood in terms of a Teleological (rather than a Turing Machine) notion of function. However, functionalism does not emerge totally unscathed. Voltaire's Dr. Pangloss saw everything in terms of its function and its perfect performance of its function. In the philosophy of mind, his influence lives on in the form of two ideas: (i) that we must possess rational methods for constructing beliefs, since our minds are the product of natural selection, and (ii) that psychological states and properties are individuated by their psychological functions. Contemporary biology provides the resources for avoiding Pangloss's wideeyed teleology in the study of adaptation. It is to be hoped that progress in psychology will loosen the grip of Panglossian assumptions in the study of mind.

Suppose that several observations “coincide,” meaning that they are similar in some interesting respect. Is this coinciding a mere coincidence, or does it derive from a common cause? Those who reason about this kind of question—whether they embrace the first answer or the second—often deploy a mode of inference that I call probabilistic modus tollens. In this chapter I criticize probabilistic modus tollens and consider likelihood and Bayesian frameworks for reasoning about coincidences. I also consider the perspective offered by model selection theory (including the Akaike information criterion), and argue that model selection often provides important insights.

Evolutionary theory is awash with probabilities. For example, natural selection is said to occur when there is variation in fitness, and fitness is standardly decomposed into two components, viability and fertility, each of which is understood probabilistically. With respect to viability, a fertilized egg is said to have a certain chance of surviving to reproductive age; with respect to fertility, an adult is said to have an expected number of offspring.1 There is more to evolutionary theory than the theory of natural selection, and here too one finds probabilistic concepts aplenty. When there is no selection, the theory of neutral evolution says that a gene’s chance of eventually reaching fixation is 1/(2N), where N is the number of organisms in the generation of the diploid population to which the gene belongs. The evolutionary consequences of mutation are likewise conceptualized in terms of the probability per unit time a gene has of changing from one state to another. The examples just mentioned are all “forwarddirected” probabilities; they describe the probability of later events, conditional on earlier events. However, evolutionary theory also uses “backwards probabilities” that describe the probability of a cause conditional on its effects; for example, coalescence theory allows one to calculate the expected number of generations in the past that the genes in the present generation find their most recent common ancestor.

The reception so far of Kitcher's Vaulting Ambition reminds me of the old saw about the difference between an optimist and a pessimist. Looking at the same glass of water, the former sees it as half full while the latter sees it as half empty. Some have seen Kitcher's book as a vindication of the possibility of an evolutionary science of human behavior; others have seen it as a devastating critique of the most influential efforts to date to construct such a science. As in the joke about the water glass, both assessments have their point. Sociobiology is a research program, not a unified theory. What one can do is test particular hypotheses within this program and see whether they live up to reasonable standards of rigor and evidence. This is what Kitcher does, with great energy and care.

It is a challenge to explain how evolutionary altruism can evolve by the process of natural selection, since altruists in a group will be less fit than the selfish individuals in the same group who receive benefits but do not make donations of their own. Darwin proposed a theory of group selection to solve this puzzle. Very simply, even though altruists are less fit than selfish individuals within any single group, groups of altruists are more fit than groups of selfish individuals. If a population is subdivided into many groups that vary in their altruistic tendencies, altruism will be favored at the level of selection among groups even as it is being disfavored at the level of selection among individuals within groups. Darwin’s scenario became the basis for a theoretical framework called multilevel selection theory.

In this brief space I want to describe how Chomsky's analysis of "psychological reality" departs from what I think is a fairly standard construal of the idea. This familiar formulation arises from distinguishing between someone's following a rule and someone's acting in conformity with a rule. The former idea, but not the latter, involves the idea that the person has some mental representation of the rule that plays a certain causal role in determining behavior. Although there may be many grammatical rules to which a person's verbal behavior (ignoring slips of the tongue and other performance interferences) conforms, only some of those rules have psychological reality; these are the ones that are internalized in thought and play some appropriate causal role.

Markov models of evolution describe changes in the probability distribution of the trait values a population might exhibit. In consequence, they also describe how entropy and conditional entropy values evolve, and how the mutual information that characterizes the relation between an earlier and a later moment in a lineage’s history depends on how much time separates them. These models therefore provide an interesting perspective on questions that usually are considered in the foundations of physics—when and why does entropy increase and at what rates do changes in entropy take place? They also throw light on an important epistemological question: are there limits on what your observations of the present can tell you about the evolutionary past?

Historical sciences like evolutionary biology reconstruct past events by using the traces that the past has bequeathed to the present. Markov chain theory entails that the passage of time reduces the amount of information that the present provides about the past. Here we use a Moran process framework to show that some evolutionary processes destroy information faster than others. Our results connect with Darwin’s principle that adaptive similarities provide scant evidence of common ancestry whereas neutral and deleterious similarities do better. We also describe how the branching in phylogenetic trees affects the information that the present supplies about the past