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  1. The maintenance of behavioral diversity in human societies.Christopher Wills - 1994 - Behavioral and Brain Sciences 17 (4):638-639.
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  • Beyond shared fate: Group-selected mechanisms for cooperation and competition in fuzzy, fluid vehicles.Geoffrey F. Miller - 1994 - Behavioral and Brain Sciences 17 (4):630-631.
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  • Replicators and vehicles? Or developmental systems?P. E. Griffiths & R. D. Gray - 1994 - Behavioral and Brain Sciences 17 (4):623-624.
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  • Driving both ways: Wilson & Sober's conflicting criteria for the identification of groups as vehicles of selection.John Alroy & Alexander Levine - 1994 - Behavioral and Brain Sciences 17 (4):608-610.
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  • Reintroducing group selection to the human behavioral sciences.David Sloan Wilson & Elliott Sober - 1994 - Behavioral and Brain Sciences 17 (4):585-608.
    In both biology and the human sciences, social groups are sometimes treated as adaptive units whose organization cannot be reduced to individual interactions. This group-level view is opposed by a more individualistic one that treats social organization as a byproduct of self-interest. According to biologists, group-level adaptations can evolve only by a process of natural selection at the group level. Most biologists rejected group selection as an important evolutionary force during the 1960s and 1970s but a positive literature began to (...)
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  • Women’s fertility across the cycle increases the short-term attractiveness of creative intelligence.Martie G. Haselton & Geoffrey F. Miller - 2006 - Human Nature 17 (1):50-73.
    Male provisioning ability may have evolved as a “good dad” indicator through sexual selection, whereas male creativity may have evolved partly as a “good genes” indicator. If so, women near peak fertility (midcycle) should prefer creativity over wealth, especially in short-term mating. Forty-one normally cycling women read vignettes describing creative but poor men vs. uncreative but rich men. Women’s estimated fertility predicted their short-term (but not long-term) preference for creativity over wealth, in both their desirability ratings of individual men (r=.40, (...)
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  • Do high-status people really have fewer children?Jason Weeden, Michael J. Abrams, Melanie C. Green & John Sabini - 2006 - Human Nature 17 (4):377-392.
    Evolutionary discussions regarding the relationship between social status and fertility in the contemporary U.S. typically claim that the relationship is either negative or absent entirely. The published data on recent generations of Americans upon which such statements rest, however, are solid with respect to women but sparse and equivocal for men. In the current study, we investigate education and income in relation to age at first child, childlessness, and number of children for men and women in two samples—one of the (...)
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  • Sexual selection and physical attractiveness.Steven W. Gangestad - 1993 - Human Nature 4 (3):205-235.
    Sexual selection processes have received much attention in recent years, attention reflected in interest in human mate preferences. Among these mate preferences are preferences for physical attractiveness. Preferences in and of themselves, however, do not fully explain the nature of the relationships that individuals attain. A tacit negotiation process underlies relationship formation and maintenance. The notion that preferences for physical attractiveness evolved under parasite-driven “good genes” sexual selection leads to predictions about the nature of trade-offs that individuals make between mates’ (...)
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  • Psychopathology: Type or trait?H. J. Eysenck - 1995 - Behavioral and Brain Sciences 18 (3):555-556.
    Mealey proposes two categorical classes of sociopath, primary and secondary. I criticize this distinction on the basis that constructs of this kind have proved unrealistic in personality taxonomy and that dimensional systems capture reality much more successfully. I suggest how such a system could work in this particular context.
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  • An evaluation of Mealey's hypotheses based on psychopathy checklist: Identified groups.David S. Kosson & Joseph P. Newman - 1995 - Behavioral and Brain Sciences 18 (3):562-563.
    Although Mealey's account provides several interesting hypotheses, her integration across disparate samples renders the value of her explanation for psychopathy ambiguous. Recent evidence on Psychopathy Checklist-identified samples (Hare, 1991) suggests primary emotional and cognitive deficits inconsistent with her model. Whereas high-anxious psychopaths display interpersonal deficits consistent with Mealey's hypotheses, low-anxious psychopaths' deficits appear more sensitive to situational parameters than predicted.
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  • Adaptive and nonadaptive explanations of sociopathy.Chris Moore & Michael R. Rose - 1995 - Behavioral and Brain Sciences 18 (3):566-567.
    We doubt that primary sociopathy is adaptive, for three reasons: First, its prevalence is too low to require an adaptive explanation. Second, a common sequela of damage to the orbito-frontal lobes is Any pattern of behavior that can be produced by brain damage is unlikely to be adaptive. Third, we argue that most human social behavior is not under tight genetic control, but is produced by open-ended calculation of fitness-contingencies.
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  • Extending arousal theory and reflecting on biosocial approaches to social science.Lee Ellis - 1995 - Behavioral and Brain Sciences 18 (3):554-554.
    This commentary extends arousal theory to suggest an explanation for the well-established inverse correlation between church attendance and involvement in crime. In addition, the results of two surveys of social scientists are reviewed to reveal just how little impact the biosocial/sociobiological perspective has had thus far on social science.
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  • Group differences ≢ individual differences.C. S. Bergeman & A. D. Seroczynski - 1995 - Behavioral and Brain Sciences 18 (3):546-548.
    Mealey's etiological distinction between primary and secondary sociopathy blurs the delineation between individual and group differences. She uses physiological evidence to support her claim of genetic influences, neglecting variability within social classes, frequency of delinquent behavior in upper and middle classes (measured by self-report), and discontinuity of criminal behavior across the life span. Finally, Mealey's proposals for differential intervention fall short of a future agenda, which should tailor to individual needs, not social classes.
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  • Primary sociopathy (psychopathy) is a type, secondary is not.Linda Mealey - 1995 - Behavioral and Brain Sciences 18 (3):579-599.
    Recent studies lend support to the two-pathway model of the evolution of sociopathy with evidence that: 1) psychopathy (primary sociopathy) is a discrete type and 2) in general, sociopaths have relatively high levels of reproductive success. Hare's Psychopathy Checklist may provide a start for the revision of terminology that will be necessary to distinguish between primary and secondary trajectories.
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  • Genetic issues in “the sociobiology of sociopathy”.Stephen C. Maxson - 1995 - Behavioral and Brain Sciences 18 (3):565-565.
    A consideration of the genetics of sociopathy suggests the following. The author's Evolutionary Stable Strategy (ESS) types 2 to 4 are more likely than types 1 and 5 in crimes of violence, and there may not be an ESS for crimes of property or for sociopathy. Correlations between sociopathy and crimes of property are also more likely due to environmental than to genetic variants, and correlations between sociopathy and crimes of property are due more to environmental than genetic variants.
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  • The sociobiology of sociopathy: An integrated evolutionary model.Linda Mealey - 1995 - Behavioral and Brain Sciences 18:523-541.
    Sociopaths are “outstanding” members of society in two senses: politically, they draw our attention because of the inordinate amount of crime they commit, and psychologically, they hold our fascination because most ofus cannot fathom the cold, detached way they repeatedly harm and manipulate others. Proximate explanations from behavior genetics, child development, personality theory, learning theory, and social psychology describe a complex interaction of genetic and physiological risk factors with demographic and micro environmental variables that predispose a portion of the population (...)
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  • The evolution of human mating: Trade-offs and strategic pluralism.Steven W. Gangestad & Jeffry A. Simpson - 2000 - Behavioral and Brain Sciences 23 (4):573-587.
    During human evolutionary history, there were “trade-offs” between expending time and energy on child-rearing and mating, so both men and women evolved conditional mating strategies guided by cues signaling the circumstances. Many short-term matings might be successful for some men; others might try to find and keep a single mate, investing their effort in rearing her offspring. Recent evidence suggests that men with features signaling genetic benefits to offspring should be preferred by women as short-term mates, but there are trade-offs (...)
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  • Seeing the light: What does biology tell us about human social behavior?C. Daniel Batson - 1994 - Behavioral and Brain Sciences 17 (4):610-611.
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  • Prestige, possessions, and progeny.Michael J. Casimir & Aparna Rao - 1995 - Human Nature 6 (3):241-272.
    It has been suggested by some that the acquisition of symbolic capital in terms of honor, prestige, and power translates into an accumulation of material capital in terms of tangible belongings, and that on the basis of these goods high reproductive success may be achieved. However, data on completed fertility rates over more than one generation in so-called traditional societies have been rare. Ethnographic and demographic data presented here on the pastoral Bakkarwal of northern India largely corroborate the hypothesis concerning (...)
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  • Mate choice in modern societies.Daniel Pérusse - 1994 - Human Nature 5 (3):255-278.
    Most research on mate choice in modern societies is based on data that may or may not reflect actual mating behavior (e.g., stated preferences, personal advertisements). In the present study, real-life matings were reported by a large representative sample of men and women (N = 1,133). These data were used to test an evolutionary model in which mate choice is hypothesized to depend on resources potentially contributed to reproduction by each sex. Consistent with the model, it was found that (a) (...)
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  • The primary/secondary distinction of psychopathy: A clinical perspective.Gisli H. Gudjonsson - 1995 - Behavioral and Brain Sciences 18 (3):558-559.
    In this brief commentary the author concentrates on the treatment perspectives of Mealey's model. The main weakness of the model is that it does not provide a satisfactory theoretical connection between treatment and different types of target behavior. Even within the primary-secondary distinction, there are large individual differences that should not be overlooked in the planning of treatment.
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  • Diathesis stress model or “Just So” story?Richard M. McFall, James T. Townsend & Richard J. Viken - 1995 - Behavioral and Brain Sciences 18 (3):565-566.
    Mealey's sociopathy model is an exemplar of popular diathesis-stress models. Although such models, when presented in descriptive language, offer the illusion of integrative explanation, their actual scientific value is very limited because they fail to make specific, quantitative, falsifiable predictions. Conceptual and quantitative weaknesses of such diathesis-stress models are discussed and the requirements for useful models are outlined.
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  • Implications of an evolutionary biopsychosocial model.Harmon R. Holcomb - 1995 - Behavioral and Brain Sciences 18 (3):559-560.
    Mealey's work has several interesting implications: It refutes the charge that sociobiology paints a cynical portrait of human nature and adopts a one-sided reductionism; it exemplifies a general theoretical scheme for constructing evolutionary biopsychosocial models of human behavior; and it has the practical effect of promoting and informing early intervention in children at risk for psychopathic disorder.
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  • Psychopathy and violence: Arousal, temperament, birth complications, maternal rejection, and prefrontal dysfunction.Adrian Raine - 1995 - Behavioral and Brain Sciences 18 (3):571-573.
    The key questions arising from Mealey's analysis are: Do environmental factors such as early maternal rejection also contribute to the emotional deficits observed in psychopaths? Are there psychophysiological protective factors for antisocial behavior that have clinical implications? Does a disinhibited temperament and low arousal predispose to primary psychopathy? Would primary or secondary psychopaths be most characterized by prefrontal dysfunction?
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  • Sociopathy, evolution, and the brain.Ernest S. Barratt & Russell Gardner - 1995 - Behavioral and Brain Sciences 18 (3):544-544.
    We propose that Mealey's model is limited in its description of sociopathy because it does not provide an adequate role for the main organ mediating genes and behavior, namely, the brain. Further, on the basis of our research, we question the view of sociopaths as a homogeneous group.
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  • The role of emotion in sociopathy: Contradictions and unanswered questions.Nancy Eisenberg - 1995 - Behavioral and Brain Sciences 18 (3):553-554.
    Emotion is critical in Mealey's conceptual arguments. However, several of her assertions about the role of emotion in sociopathy are problematic. Questions are raised regarding the link between lack of anxiety and low levels of secondary emotions such as love and sympathy, the argument that sociopaths are low in anxiety but high in neuroticism, and the designation of anxiety as a secondary emotion.
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  • Genes, hormones, and gender in sociopathy.Katharine Hoyenga - 1995 - Behavioral and Brain Sciences 18 (3):560-560.
    Although serotonin, testosterone, and genes contribute to sociopathy, the relationships are probably indirect and subject to modifiers (e.g., present only under certain conditions of rearing and temperament). Age at menarche may be a marker variable as well as a causal factor. Since the genders differ in all four areas, sex differences in sociopathy represent a very complex interaction of these factors.
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  • Emotions and sociopathy.Robert Plutchik - 1995 - Behavioral and Brain Sciences 18 (3):570-571.
    Questions are raised about several issues discussed by Mealey: (1) the nature of the distinction between primary and secondary sociopaths, (2) some difficulties with a general arousal theory of criminality, and (3) the possible role of countervailing forces in the development of sociopathy. An important area that calls for attention is the patterning of different specific emotions in the lives of sociopaths as compared to other groups.
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  • Why some Apes became Humans, Competition, consciousness, and culture.Pouwel Slurink - 2002 - Dissertation, Radboud University
    Chapter 1 (To know in order to survive) & Chapter 2 (A critique of evolved reason) explain human knowledge and its limits from an evolutionary point of view. Chapter 3 (Captured in our Cockpits) explains the evolution of consciousness, using value driven decision theory. Chapter 4-6 (Chapter 4 Sociobiology, Chapter 5 Culture: the Human Arena), Chapter 6, Genes, Memes, and the Environment) show that to understand culture you have at least to deal with 4 levels: genes, brains, the environment, culture. (...)
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  • Group selection: The theory replaces the bogey man.David Sloan Wilson & Elliott Sober - 1994 - Behavioral and Brain Sciences 17 (4):639-654.
    In both biology and the human sciences, social groups are sometimes treated as adaptive units whose organization cannot be reduced to individual interactions. This group-level view is opposed by a more individualistic one that treats social organization as a byproduct of self-interest. According to biologists, group-level adaptations can evolve only by a process of natural selection at the group level. Most biologists rejected group selection as an important evolutionary force during the 1960s and 1970s but a positive literature began to (...)
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  • Groups as vehicles and replicators: The problem of group-level adaptation.Kent E. Holsinger - 1994 - Behavioral and Brain Sciences 17 (4):626-627.
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  • Metaphors and mechanisms in vehicle-based selection theory.Michael Bradie - 1994 - Behavioral and Brain Sciences 17 (4):612-612.
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  • Moral judgments by alleged sociopaths as a means for coping with problems of definition and identification in Mealey's model.Yuval Wolf - 1995 - Behavioral and Brain Sciences 18 (3):577-578.
    Problems of definition and identification in the integrated evolutionary model of sociopathy are suggested by Schoenfeld's (1974) criticism of the field of race differences in intelligence. Moral judgments by those labeled primary and secondary sociopaths may offer a way to validate the assumptions of the model.
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  • Niche construction: A pervasive force in evolution?Wim J. van der Steen - 2000 - Behavioral and Brain Sciences 23 (1):162-163.
    Industrial melanism, according to the traditional explanation, amounts to niche construction since it involves changes in predation pressure. Indeed, it would be difficult to imagine selection without niche construction. This cannot be what Laland, Odling-Smee & Feldman mean. They offer convincing examples, but they should provide a better definition of “niche construction” to indicate how their view supplements traditional evolutionary biology.
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  • Semantics, theory, and methodological individualism in the group-selection controversy.Eric Alden Smith - 1994 - Behavioral and Brain Sciences 17 (4):636-637.
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  • Reconstructing the real unit of selection.Adolf Heschl - 1994 - Behavioral and Brain Sciences 17 (4):624-625.
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  • Taking vechicles seriously.David L. Hull - 1994 - Behavioral and Brain Sciences 17 (4):627-628.
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  • Different vehicles for group selection in humans.Michael E. Hyland - 1994 - Behavioral and Brain Sciences 17 (4):628-628.
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  • Does observed fertility maximize fitness among New Mexican men?Hillard S. Kaplan, Jane B. Lancaster, Sara E. Johnson & John A. Bock - 1995 - Human Nature 6 (4):325-360.
    Our objective is to test an optimality model of human fertility that specifies the behavioral requirements for fitness maximization in order (a) to determine whether current behavior does maximize fitness and, if not, (b) to use the specific nature of the behavioral deviations from fitness maximization towards the development of models of evolved proximate mechanisms that may have maximized fitness in the past but lead to deviations under present conditions. To test the model we use data from a representative sample (...)
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  • Sociopathy and sociobiology: Biological units and behavioral units.Carl J. Erickson - 1995 - Behavioral and Brain Sciences 18 (3):555-555.
    Behavioral biologists have long sought to link behavioral units (e.g., aggression, depression, sociopathy) with biological units (e.g., genes, neurotransmitters, hormones, neuroanatomical loci). These units, originally contrived for descriptive purposes, often lead to misunderstandings when they are reified for purposes of causal analysis. This genetic and biochemical explanation for sociopathy reflects such problems.
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  • Psychopathy is a nonarbitrary class.Vernon L. Quinsey & Martin L. Lalumière - 1995 - Behavioral and Brain Sciences 18 (3):571-571.
    Recent evidence that psychopathy is a nonarbitrary population, such that the trait may be categorical rather than continuous, is consistent with Mealey's distinction between primary and secondary psychopaths. Thus, there are likely to be at least two routes to criminality, and psychopathic and nonpsychopathic criminals are likely to respond differently to interventions.
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  • Putting cognition into sociopathy.R. J. R. Blair & John Morton - 1995 - Behavioral and Brain Sciences 18 (3):548-548.
    We make three suggestions with regard to Mealey's work. First, her lack of a cognitive analysis of the sociopath results in underspecified mappings between sociobiology and behavior. Second, the developmental literature indicates that Mealey's implicit assumption, that moral socialisation is achieved through punishment, is invalid. Third, we advance the use of causal modelling to map the developmental relationships between biology, cognition, and behaviour.
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  • Birth order, sibship size, and status in modern Canada.Jennifer Nerissa Davis - 1997 - Human Nature 8 (3):205-230.
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  • Interdiscourse or supervenience relations: The primacy of the manifest image.J. Brakel - 1996 - Synthese 106 (2):253 - 297.
    Amidst the progress being made in the various (sub-)disciplines of the behavioural and brain sciences a somewhat neglected subject is the problem of how everything fits into one world and, derivatively, how the relation between different levels of discourse should be understood and to what extent different levels, domains, approaches, or disciplines are autonomous or dependent. In this paper I critically review the most recent proposals to specify the nature of interdiscourse relations, focusing on the concept of supervenience. Ideally supervenience (...)
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  • Putting the cart back behind the horse: Group selection does not require that groups be “organisms”.Todd A. Grantham - 1994 - Behavioral and Brain Sciences 17 (4):622-623.
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  • Group evolutionary strategies: Dimensions and mechanisms.Kevin MacDonald - 1994 - Behavioral and Brain Sciences 17 (4):629-630.
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  • Sociopathy or hyper-masculinity?Anne Campbell - 1995 - Behavioral and Brain Sciences 18 (3):548-549.
    Definitional slippage threatens to equate secondary sociopathy with mere criminality and leaves the status of noncriminal sociopaths ambiguous. Primary sociopathy appears to show more environmental contingency than would be implied by a strong genetic trait approach. A reinterpretation in terms of hypermasculinity and hypofemininity is compatible with the data.
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  • Is the distinction between primary and secondary sociopaths a matter of degree, secondary traits, or nature vs. nurture?Marvin Zuckerman - 1995 - Behavioral and Brain Sciences 18 (3):578-579.
    Psychopathy has as its central traits socialization, sensation seeking, and impulsivity. These are combined in a supertrait: Impulsive Unsocialized Sensation Seeking (ImpUSS). Secondary types are defined by combinations of ImpUSS and neuroticism or sociability. All broad personality traits have both genetic and environmental determination, and therefore different etiologies (primary as genetic, secondary as environmental) for primary and secondary sociopathy are unlikely.
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  • (1 other version)Eric Alden Smith and Bruce winterhalder, eds., Evolutionary ecology and human behavior. Aldine de gruyter, new York, 1992. Pp. XV, 470, tables, boxes, figures, bibliography, author index, subject index. $59.95 (cloth), $29.95 (paper. [REVIEW]Andrew P. Vayda - 1995 - Philosophy of the Social Sciences 25 (2):219-249.
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  • Nongenetic and non-Darwinian evolution.Anatol Rapoport - 1994 - Behavioral and Brain Sciences 17 (4):634-634.
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