Elliott Sober

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.

Evolutionary gradualism, the randomness of mutations, and the hypothesis that natural selection exerts a pervasive and substantial influence on evolutionary outcomes are pair-wise logically independent. Can the claims about selection and mutation be used to formulate an argument for gradualism? In his Genetical Theory of Natural Selection, R.A. Fisher made an important start at this project in his famous “geometric argument” by showing that a random mutation that has a smaller effect on two or more phenotypes will have a higher average fitness than a random mutation that has a larger phenotypic effect. Motoo Kimura’s demonstration that a gene’s probability of fixation depends on both the selection coefficient and the effective population size shows that Fisher’s argument for gradualism was mistaken. Here we analyze Fisher’s argument and explain how Kimura’s theory leads to a conclusion that Fisher did not anticipate. We identify a fallacy that reasoning about fitness differences and their evolutionary consequences should avoid. We then distinguish forward-directed from backward-directed versions of gradualism. The backward-directed thesis about a single mutation may be correct, but the forward-directed thesis is not. After that we consider a sequence of random mutations that all affect the same cluster of phenotypes and Allen Orr’s idea that there is an optimal sequence of mutation sizes, moving from larger to smaller as the population approaches a fixed optimum. This provides a likelihood justification for a forward-directed version of gradualism when there is a fixed optimum, but it also provides an argument against forward-directed gradualism if the optimum shifts substantially as the population evolves. Finally, we consider whether genome-wide association studies (GWASs) can furnish empirical evidence that bears on the truth of gradualism. The version of gradualism that GWASs directly bear on concerns the phenotypic effect size of a gene after it arises by mutation and has reached an appreciable frequency, not the phenotypic size of the mutation event itself.

Writing in an engaging lecture-style format, Elliott Sober shows students how philosophy is best used to evaluate many different kinds of arguments and to construct sound theories. Well-known arguments and problems from the history of philosophy are discussed and analyzed, not as a means to honor the dead or merely to discuss what various philosophers have thought, but to engage with, criticize, and even improve ideas from the past. In addition--because philosophy cannot function apart from its engagement with the wider society--traditional and contemporary philosophical problems are brought into dialogue with the physical, biological, and social sciences. Text boxes highlight key concepts, and review questions, discussion questions, and a glossary of terms are also included. Core Questions in Philosophyhas served as a premier introductory textbook for more than two decades, with updates to each new edition. New improvements to this seventh edition include a lower price and a new Routledge companion website that includes: Updated Supplementary Readings, with the inclusion of more work from female philosophers New videos and podcasts, organized by their relevance to each chapter in the book. Visit the companion website at: www.routledge.com/cw/sober.

Do the methods of science lead to atheism? This is different from asking whether the results of science (e.g., well‐confirmed theories in evolutionary biology or cosmology) have that consequence. In this chapter, I consider several philosophical theories about scientific reasoning and trace out their implications for atheism, theism, and agnosticism. These theories include different versions of empiricism, logical positivism, inference to the best explanation, Bayesianism, hypothetico‐deductivism, and the principle of parsimony (Ockham's razor).

Is it accurate to label Darwin's theory "the theory of evolution by natural selection," given that the concept of common ancestry is at least as central to Darwin's theory? Did Darwin reject the idea that group selection causes characteristics to evolve that are good for the group though bad for the individual? How does Darwin's discussion of God in The Origin of Species square with the common view that he is the champion of methodological naturalism? These are just some of the intriguing questions raised in this volume of interconnected philosophical essays on Darwin. The author's approach is informed by modern issues in evolutionary biology, but is sensitive to the ways in which Darwin's outlook differed from that of many biologists today. The main topics that are the focus of the book--common ancestry, group selection, sex ratio, and naturalism--have rarely been discussed in their connection with Darwin in such penetrating detail.

Perhaps because of it implications for our understanding of human nature, recent philosophy of biology has seen what might be the most dramatic work in the philosophies of the ?special? sciences. This drama has centered on evolutionary theory, and in the second edition of this textbook, Elliott Sober introduces the reader to the most important issues of these developments. With a rare combination of technical sophistication and clarity of expression, Sober engages both the higher level of theory and the direct implications for such controversial issues as creationism, teleology, nature versus nurture, and sociobiology. Above all, the reader will gain from this book a firm grasp of the structure of evolutionary theory, the evidence for it, and the scope of its explanatory significance.

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.

The debate over the relative importance of natural selection as compared to other forces affecting the evolution of organisms is a long-standing and central controversy in evolutionary biology. The theory of adaptationism argues that natural selection contains sufficient explanatory power in itself to account for all evolution. However, there are differing views about the efficiency of the adaptation model of explanation. If the adaptationism theory is applied, are energy and resources being used to their optimum? This book presents an up-to-date view of this controversy and reflects the dramatic changes in our understanding of evolution that have occurred in the last twenty years. The volume combines contributions from biologists and philosophers, and offers a systematic treatment of foundational, conceptual, and methodological issues surrounding the theory of adaptationism. The essays examine recent developments in topics such as phylogenetic analysis, the theory of optimality and ess models, and methods of testing models.

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.

The argument from design is best understood as a likelihood inference. Its Achilles heel is our lack of knowledge concerning the aims and abilities that the putative designer would have; in consequence, it is impossible to determine whether the observations are more probable under the design hypothesis than they are under the hypothesis of chance. Hypotheses about the role played by natural selection in the history of life also can be evaluated within a likelihood framework, and here too there are auxiliary assumptions that need to be in place if the likelihoods of selection and chance are to be compared. I describe some problems that arise in connection with the project of obtaining independent evidence concerning those auxiliary assumptions.

Psychological egoism is a theory about motivation. It claims that all of our ultimate desires are self‐directed. Whenever we want others to do well (or ill), we have these other‐directed desires only instrumentally; we care about others only because we think that the welfare of others will have ramifications for our own welfare. As stated, egoism is a descriptive, not a normative, claim. It aims to characterize what motivates human beings in fact; the theory does not say whether it is good or bad that people are so motivated.

In this paper, I'll explore three contexts in which the heuristic of personification yields the wrong answer. They all come from game theoretic discussion of altruism and the Prisoner's Dilemma. Whether it is applied to evolution or to rational deliberation, game theory models situations that involve frequency dependence. In the evolutionary case, how fit a trait is, and whether it is more or less fit than the alternatives, depends on the composition of the population (Maynard Smith 1982). In the case of rational deliberation, which act is best for the agent depends on what other actors are likely to do. As we now will see, frequency dependence can throw a monkey wrench into the convenient relationship between deliberation and evolution posited by the heuristic of personification.

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.