Sociobiology
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Sociobiology

The New Synthesis, Twenty-Fifth Anniversary Edition

Edward O. Wilson

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eBook - ePub

Sociobiology

The New Synthesis, Twenty-Fifth Anniversary Edition

Edward O. Wilson

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When this classic work was first published in 1975, it created a new discipline and started a tumultuous round in the age-old nature versus nurture debate. Although voted by officers and fellows of the international Animal Behavior Society the most important book on animal behavior of all time, Sociobiology is probably more widely known as the object of bitter attacks by social scientists and other scholars who opposed its claim that human social behavior, indeed human nature, has a biological foundation. The controversy surrounding the publication of the book reverberates to the present day.In the introduction to this Twenty-Fifth Anniversary Edition, Edward O. Wilson shows how research in human genetics and neuroscience has strengthened the case for a biological understanding of human nature. Human sociobiology, now often called evolutionary psychology, has in the last quarter of a century emerged as its own field of study, drawing on theory and data from both biology and the social sciences.For its still fresh and beautifully illustrated descriptions of animal societies, and its importance as a crucial step forward in the understanding of human beings, this anniversary edition of Sociobiology: The New Synthesis will be welcomed by a new generation of students and scholars in all branches of learning.

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Información

Editorial
Belknap Press
Año
2000
ISBN
9780674744172
Categoría
Evolution
Part I Social Evolution
Chapter 1 The Morality of the Gene
Camus said that the only serious philosophical question is suicide. That is wrong even in the strict sense intended. The biologist, who is concerned with questions of physiology and evolutionary history, realizes that self-knowledge is constrained and shaped by the emotional control centers in the hypothalamus and limbic system of the brain. These centers flood our consciousness with all the emotions—hate, love, guilt, fear, and others—that are consulted by ethical philosophers who wish to intuit the standards of good and evil. What, we are then compelled to ask, made the hypothalamus and limbic system? They evolved by natural selection. That simple biological statement must be pursued to explain ethics and ethical philosophers, if not epistemology and epistemologists, at all depths. Self-existence, or the suicide that terminates it, is not the central question of philosophy. The hypothalamic-limbic complex automatically denies such logical reduction by countering it with feelings of guilt and altruism. In this one way the philosopher’s own emotional control centers are wiser than his solipsist consciousness, “knowing” that in evolutionary time the individual organism counts for almost nothing. In a Darwinist sense the organism does not live for itself. Its primary function is not even to reproduce other organisms; it reproduces genes, and it serves as their temporary carrier. Each organism generated by sexual reproduction is a unique, accidental subset of all the genes constituting the species. Natural selection is the process whereby certain genes gain representation in the following generations superior to that of other genes located at the same chromosome positions. When new sex cells are manufactured in each generation, the winning genes are pulled apart and reassembled to manufacture new organisms that, on the average, contain a higher proportion of the same genes. But the individual organism is only their vehicle, part of an elaborate device to preserve and spread them with the least possible biochemical perturbation. Samuel Butler’s famous aphorism, that the chicken is only an egg’s way of making another egg, has been modernized: the organism is only DNA’s way of making more DNA. More to the point, the hypothalamus and limbic system are engineered to perpetuate DNA.
In the process of natural selection, then, any device that can insert a higher proportion of certain genes into subsequent generations will come to characterize the species. One class of such devices promotes prolonged individual survival. Another promotes superior mating performance and care of the resulting offspring. As more complex social behavior by the organism is added to the genes’ techniques for replicating themselves, altruism becomes increasingly prevalent and eventually appears in exaggerated forms. This brings us to the central theoretical problem of sociobiology: how can altruism, which by definition reduces personal fitness, possibly evolve by natural selection? The answer is kinship: if the genes causing the altruism are shared by two organisms because of common descent, and if the altruistic act by one organism increases the joint contribution of these genes to the next generation, the propensity to altruism will spread through the gene pool. This occurs even though the altruist makes less of a solitary contribution to the gene pool as the price of its altruistic act.
To his own question, “Does the Absurd dictate death?” Camus replied that the struggle toward the heights is itself enough to fill a man’s heart. This arid judgment is probably correct, but it makes little sense except when closely examined in the light of evolutionary theory. The hypothalamic-limbic complex of a highly social species, such as man, “knows,” or more precisely it has been programmed to perform as if it knows, that its underlying genes will be proliferated maximally only if it orchestrates behavioral responses that bring into play an efficient mixture of personal survival, reproduction, and altruism. Consequently, the centers of the complex tax the conscious mind with ambivalences whenever the organisms encounter stressful situations. Love joins hate; aggression, fear; expansiveness, withdrawal; and so on; in blends designed not to promote the happiness and survival of the individual, but to favor the maximum transmission of the controlling genes.
The ambivalences stem from counteracting pressures on the units of natural selection. Their genetic consequences will be explored formally later in this book. For the moment suffice it to note that what is good for the individual can be destructive to the family; what preserves the family can be harsh on both the individual and the tribe to which its family belongs; what promotes the tribe can weaken the family and destroy the individual; and so on upward through the permutations of levels of organization. Counteracting selection on these different units will result in certain genes being multiplied and fixed, others lost, and combinations of still others held in static proportions. According to the present theory, some of the genes will produce emotional states that reflect the balance of counteracting selection forces at the different levels.
I have raised a problem in ethical philosophy in order to characterize the essence of sociobiology. Sociobiology is defined as the systematic study of the biological basis of all social behavior. For the present it focuses on animal societies, their population structure, castes, and communication, together with all of the physiology underlying the social adaptations. But the discipline is also concerned with the social behavior of early man and the adaptive features of organization in the more primitive contemporary human societies. Sociology sensu stricto, the study of human societies at all levels of complexity, still stands apart from sociobiology because of its largely structuralist and nongenetic approach. It attempts to explain human behavior primarily by empirical description of the outermost phenotypes and by unaided intuition, without reference to evolutionary explanations in the true genetic sense. It is most successful, in the way descriptive taxonomy and ecology have been most successful, when it provides a detailed description of particular phenomena and demonstrates first-order correlations with features of the environment. Taxonomy and ecology, however, have been reshaped entirely during the past forty years by integration into neo-Darwinist evolutionary theory—the “Modern Synthesis,” as it is often called—in which each phenomenon is weighed for its adaptive significance and then related to the basic principles of population genetics. It may not be too much to say that sociology and the other social sciences, as well as the humanities, are the last branches of biology waiting to be included in the Modern Synthesis. One of the functions of sociobiology, then, is to reformulate the foundations of the social sciences in a way that draws these subjects into the Modern Synthesis. Whether the social sciences can be truly biologicized in this fashion remains to be seen.
This book makes an attempt to codify sociobiology into a branch of evolutionary biology and particularly of modern population biology. I believe that the subject has an adequate richness of detail and aggregate of self-sufficient concepts to be ranked as coordinate with such disciplines as molecular biology and developmental biology. In the past its development has been slowed by too close an identification with ethology and behavioral physiology. In the view presented here, the new sociobiology should be compounded of roughly equal parts of invertebrate zoology, vertebrate zoology, and population biology. Figure 1-1 shows the schema with which I closed The Insect Societies, suggesting how the amalgam can be achieved. Biologists have always been intrigued by comparisons between societies of invertebrates, especially insect societies, and those of vertebrates. They have dreamed of identifying the common properties of such disparate units in a way that would provide insight into all aspects of social evolution, including that of man. The goal can be expressed in modern terms as follows: when the same parameters and quantitative theory are used to analyze both termite colonies and troops of rhesus macaques, we will have a unified science of sociobiology. This may seem an impossibly difficult task. But as my own studies have advanced, I have been increasingly impressed with the functional similarities between invertebrate and vertebrate societies and less so with the structural differences that seem, at first glance, to constitute such an immense gulf between them. Consider for a moment termites and monkeys. Both are formed into cooperative groups that occupy territories. The group members communicate hunger, alarm, hostility, caste status or rank, and reproductive status among themselves by means of something on the order of 10 to 100 nonsyntactical signals. Individuals are intensely aware of the distinction between groupmates and nonmembers. Kinship plays an important role in group structure and probably served as a chief generative force of sociality in the first place. In both kinds of society there is a well-marked division of labor, although in the insect society there is a much stronger reproductive component. The details of organization have been evolved by an evolutionary optimization process of unknown precision, during which some measure of added fitness was given to individuals with cooperative tendencies—at least toward relatives. The fruits of cooperativeness depend upon the particular conditions of the environment and are available to only a minority of animal species during the course of their evolution.
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Figure 1-1 The connections that can be made between phylogenetic studies, ecology, and sociobiology.
This comparison may seem facile, but it is out of such deliberate oversimplification that the beginnings of a general theory are made. The formulation of a theory of sociobiology constitutes, in my opinion, one of the great manageable problems of biology for the next twenty or thirty years. The prolegomenon of Figure 1-1 guesses part of its future outline and some of the directions in which it is most likely to lead animal behavior research. Its central precept is that the evolution of social behavior can be fully comprehended only through an understanding, first, of demography, which yields the vital information concerning population growth and age structure, and, second, of the genetic structure of the populations, which tells us what we need to know about effective population size in the genetic sense, the coefficients of relationship within the societies, and the amounts of gene flow between them. The principal goal of a general theory of sociobiology should be an ability to predict features of social organization from a knowledge of these population parameters combined with information on the behavioral constraints imposed by the genetic constitution of the species. It will be a chief task of evolutionary ecology, in turn, to derive the population parameters from a knowledge of the evolutionary history of the species and of the environment in which the most recent segment of that history unfolded. The most important feature of the prolegomenon, then, is the sequential relation between evolutionary studies, ecology, population biology, and sociobiology.
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Figure 1-2 A subjective conception of the relative number of ideas in various disciplines in and adjacent to behavioral biology to the present time and as it might be in the future.
In stressing the tightness of this sequence, however, I do not wish to underrate the filial relationship that sociobiology has had in the past with the remainder of behavioral biology. Although behavioral biology is traditionally spoken of as if it were a unified subject, it is now emerging as two distinct disciplines centered on neurophysiology and on sociobiology, respectively. The conventional wisdom also speaks of ethology, which is the naturalistic study of whole patterns of animal behavior, and its companion enterprise, comparative psychology, as the central, unifying fields of behavioral biology. They are not; both are destined to be cannibalized by neurophysiology and sensory physiology from one end and sociobiology and behavioral ecology from the other (see Figure 1-2).
I hope not too many scholars in ethology and psychology will be offended by this vision of the future of behavioral biology. It seems to be indicated both by the extrapolation of current events and by consideration of the logical relationship behavioral biology holds with the remainder of science. The future, it seems clear, cannot be with the ad hoc terminology, crude models, and curve fitting that characterize most of contemporary ethology and comparative psychology. Whole patterns of animal behavior will inevitably be explained within the framework, first, of integrative neurophysiology, which classifies neurons and reconstructs their circuitry, and, second, of sensory physiology, which seeks to characterize the cellular transducers at the molecular level. Endocrinology will continue to play a peripheral role, since it is concerned with the cruder tuning devices of nervous activity. To pass from this level and reach the next really distinct discipline, we must travel all the way up to the society and the population. Not only are the phenomena best described by families of models different from those of cellular and molecular biology, but the explanations become largely evolutionary. There should be nothing surprising in this distinction. It is only a reflection of the larger division that separates the two greater domains of evolutionary biology and functional biology. As Lewontin (1972a) has truly said: “Natural selection of the character states themselves is the essence of Darwinism. All else is molecular biology.”
Chapter 2 Elementary Concepts of Sociobiology
Genes, like Leibnitz’s monads, have no windows; the higher properties of life are emergent. To specify an entire cell, we are compelled to provide not only the nucleotide sequences but also the identity and configuration of other kinds of molecules placed in and around the cell. To specify an organism requires still more information about both the properties of the cells and their spatial positions. And once assembled, organisms have no windows. A society can be described only as a set of particular organisms, and even then it is difficult to extrapolate the joint activity of this ensemble from the instant of specification, that is, to predict social behavior. To cite one concrete example, Maslow (1936) found that the dominance relations of a group of rhesus monkeys cannot be predicted from the interactions of its members matched in pairs. Rhesus monkeys, like other higher primates, are intensely affected by their social environment—an isolated individual will repeatedly pull a lever with no reward other than the glimpse of another monkey (Butler, 1954). Moreover, this behavior is subject to higher-order interactions. The monkeys form coalitions in the struggle for dominance, so that an individual falls in rank if deprived of its allies. A second-ranking male, for example, may owe its position to protection given it by the alpha male or support from one or more close peers (Hall and DeVore, 1965; Varley and Symmes, 1966). Such coalitions cannot be predicted from the outcome of pairwise encounters, let alone from the behavior of an isolated monkey.
The recognition and study of emergent properties is holism, once a burning subject for philosophical discussion by such scientists as Lloyd Morgan (1922) and W. M. Wheeler (1927), but later, in the 1940’s and 1950’s, temporarily eclipsed by the triumphant reductionism of molecular biology. The new holism is much more quan...

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