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  1. 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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  • 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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  • Evolution, mating effort, and crime.David C. Rowe - 1995 - Behavioral and Brain Sciences 18 (3):573-574.
    Unlike some psychiatric illnesses, criminal lifestyles are not reproductive dead ends and may represent frequency-dependent adaptations. Sociopaths may gain reproductively from their greater relative to nonsociopaths. This mating-effort construct should be assessed directly in future studies of sociopathy. Collaboration between biologically oriented and environmentally oriented researchers is needed to investigate the biosocial basis of sociopathy.
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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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  • Paradox and tragedy in human morality.Pouwel Slurink - 1994 - International Political Science Review 15 (347):378.
    An evolutionary approach to ethics supports, to some extent, the sceptical meta-ethics found by some of the Greek sophists and Nietzsche. On the other hand, a modern naturalistic account on the origin and nature of morality, leads to somewhat different conclusions. This is demonstrated with an answer to three philosophical questions: does real freedom exist?, does the good, or real virtue, exist?, does life have a meaning?
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  • Sociobiological and Social Constructionist Accounts of Altruism: a Phenomenological Critique.Edwin E. Gantt & Jeffrey S. Reber - 1999 - Journal of Phenomenological Psychology 30 (2):14-38.
    Much theorizing about altruism has been undertaken within a naturalistic and deterministic sociobiological framework that has sought to explain altruistic action in terms of underlying genetic selfishness. Recently, however, social constructionist thinkers have developed an alternative to such theorizing which suggests that human action arises out of fundamentally open-ended and malleable social relationships. This paper intends to show, however, that a reductive egoism is nonetheless still at work in such accounts, typically taking the form of an underlying concern for matters (...)
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  • Romantic love and sexual desire.Aaron Ben-Ze'ev - 1997 - Philosophia 25 (1-4):3-32.
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  • Cultural group selection plays an essential role in explaining human cooperation: A sketch of the evidence.Peter Richerson, Ryan Baldini, Adrian V. Bell, Kathryn Demps, Karl Frost, Vicken Hillis, Sarah Mathew, Emily K. Newton, Nicole Naar, Lesley Newson, Cody Ross, Paul E. Smaldino, Timothy M. Waring & Matthew Zefferman - 2016 - Behavioral and Brain Sciences 39:e30.
    Human cooperation is highly unusual. We live in large groups composed mostly of non-relatives. Evolutionists have proposed a number of explanations for this pattern, including cultural group selection and extensions of more general processes such as reciprocity, kin selection, and multi-level selection acting on genes. Evolutionary processes are consilient; they affect several different empirical domains, such as patterns of behavior and the proximal drivers of that behavior. In this target article, we sketch the evidence from five domains that bear on (...)
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  • Individual differences in reproductive tactics: Cuing, assessment, and facultative strategies.Linda Mealey - 1992 - Behavioral and Brain Sciences 15 (1):105-106.
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  • Personal ads as deviant and unsatisfactory: Support for evolutionary hypotheses.D. W. Rajecki & Jeffrey Lee Rasmussen - 1992 - Behavioral and Brain Sciences 15 (1):107-107.
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  • The evolutionary model is synthetic not heuristic.P. A. Russell - 1992 - Behavioral and Brain Sciences 15 (1):108-109.
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  • Half a theory and half the data for half the people?Jeffry A. Simpson - 1992 - Behavioral and Brain Sciences 15 (1):109-110.
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  • What does evolution tell us about age preferences?Steven A. Sloman & Leon Sloman - 1992 - Behavioral and Brain Sciences 15 (1):110-111.
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  • Age preferences: The crucial studies have yet to be done.Peter Borkenau - 1992 - Behavioral and Brain Sciences 15 (1):93-94.
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  • Sex differences in age preference: Universal reality or ephemeral construction?Douglas T. Kenrick & Richard C. Keefe - 1992 - Behavioral and Brain Sciences 15 (1):119-133.
    The finding that women are attracted to men older than themselves whereas men are attracted to relatively younger women has been explained by social psychologists in terms of economic exchange rooted in traditional sex-role norms. An alternative evolutionary model suggests that males and females follow different reproductive strategies, and predicts a more complex relationship between gender and age preferences. In particular, males' preferences for relatively younger females should be minimal during early mating years, but should become more pronounced as the (...)
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  • Genetic similarity, human altruism and group selection: A study of the open peer commentaries.Klaus Jaffe - 1991 - Behavioral and Brain Sciences 14 (3):525-526.
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  • Ethnic nepotism in science?J. Philippe Rushton - 1991 - Behavioral and Brain Sciences 14 (3):526-527.
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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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  • 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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  • 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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  • Continua outperform dichotomies.John D. Baldwin - 1995 - Behavioral and Brain Sciences 18 (3):543-544.
    Mealey's data do not support her dichotomous model of primary and secondary sociopathy; this data supports the view that there is a continuum of degrees of sociopathy, from zero to the maximal manifestation. There are multitudes of factors that can contribute to sociopathy and the countless different mixes of them can produce multiple degrees and variations of sociopathic behavior.
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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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  • “Genetics” and DNA polymorphisms.Robert Plomin - 1995 - Behavioral and Brain Sciences 18 (3):570-570.
    Four questions are raised about Mealey's genetic argument: (1) Where is the evidence that secondary sociopathy is less heritable than primary sociopathy? (2) What is the genetic correlation between the two types of sociopathy? (3) How does genotype-environment interaction relate? (4) How strong are the links between our evolutionary past and current heritability?
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  • Sociobiology, sociopathy, and social policy.Richard Machalek - 1995 - Behavioral and Brain Sciences 18 (3):564-564.
    Evolutionary analysis suggests that policies based on deterrence may cope effectively with primary sociopathy if the threat of punishment fits the crime in the cost/benefit calculus of the sociopath, not that of the public. On the other hand, policies designed to offset serious disadvantage in social competition may help inhibit the development of secondary sociopathy, rather than deter its expression.
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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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  • The Homeopathy of Kin Selection: An Evaluation of van den Berghe’s Sociobiological Approach to Ethnic Nepotism.Ingo Brigandt - 2001 - Politics and the Life Sciences 20:203-215.
    The present discussion of sociobiological approaches to ethnic nepotism takes Pierre van den Berghe ʼs theory as a starting point. Two points, which have not been addressed in former analyses, are considered to be of particular importance. It is argued that the behavioral mechanism of ethnic nepotism—as understood by van den Berghe—cannot explain ethnic boundaries and attitudes. In addition, I show that van den Bergheʼs central premise concerning ethnic nepotism is in contradiction to Hamiltonʼs formula, the essential principle of kin (...)
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  • Arbitrariness and bias in evolutionary speculation.John Dupré - 1992 - Behavioral and Brain Sciences 15 (1):98-99.
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  • Obstacles to expanding human evolutionary theory.Linnda R. Caporael - 1991 - Behavioral and Brain Sciences 14 (4):750-753.
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  • Hominids, coalitions, and weapons: Not vehicles.Jim Moore - 1994 - Behavioral and Brain Sciences 17 (4):632-632.
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  • Rx: Distinguish group selection from group adaptation.Elisabeth A. Lloyd - 1994 - Behavioral and Brain Sciences 17 (4):628-629.
    I admire Wilson & Sober's (W & S's) aim, to alert social scientists that group selection has risen from the ashqs, and to explicate its relevance to the behavioral sciences. Group selection has beenwidely misunderstood; furthermore, both authors have been instrumental in illuminating conceptual problems surrounding higher-level selection. Still, I find that this target article muddies the waters, primarily through its shifting and confused definition of a "vehicle" of selection. The fundamental problem is an ambiguity in the definition of "adaptation." (...)
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  • Group selection and “genuine” altruism.Robert H. Frank - 1994 - Behavioral and Brain Sciences 17 (4):620-621.
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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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  • Perceived crime severity and biological kinship.Vernon L. Quinsey, Martin L. Lalumière, Matthew Querée & Jennifer K. McNaughton - 1999 - Human Nature 10 (4):399-414.
    Two predictions concerning the perceived severity of crimes can be derived from evolutionary theory. The first, arising from the theory of inclusive fitness, is that crimes in general should be viewed as more serious to the degree that the victim is genetically related to the perpetrator. The second, arising from the deleterious effects of inbreeding depression, is that heterosexual sexual coercion should be perceived as more serious the closer the genetic relationship of victim and perpetrator, particularly when the victim is (...)
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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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  • Human Homogamy in Facial Characteristics.Saori Nojo, Satoshi Tamura & Yasuo Ihara - 2012 - Human Nature 23 (3):323-340.
    Human homogamy may be caused in part by individuals’ preference for phenotypic similarities. Two types of preference can result in homogamy: individuals may prefer someone who is similar to themselves (self-referent phenotype matching) or to their parents (a sexual-imprinting-like mechanism). In order to examine these possibilities, we compare faces of couples and their family members in two ways. First, “perceived” similarity between a pair of faces is quantified as similarity ratings given to the pair. Second, “physical” similarity between two groups (...)
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  • Age preferences in mates reflect sex differences in human reproductive strategies.Douglas T. Kenrick & Richard C. Keefe - 1992 - Behavioral and Brain Sciences 15 (1):75-91.
    The finding that women are attracted to men older than themselves whereas men are attracted to relatively younger women has been explained by social psychologists in terms of economic exchange rooted in traditional sex-role norms. An alternative evolutionary model suggests that males and females follow different reproductive strategies, and predicts a more complex relationship between gender and age preferences. In particular, males' preferences for relatively younger females should be minimal during early mating years, but should become more pronounced as the (...)
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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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  • The sociopath: Cheater or warrior hawk?Kent G. Bailey - 1995 - Behavioral and Brain Sciences 18 (3):542-543.
    Mealey's excellent target article rests on several assumptions that may be questioned, including the overarching assumption that sociopathy reflects the failure of a small minority of males to cooperate with the larger group. I suggest that violent competition in ancestral bands cheatinggame was the primary evolutionary precursor of sociopathy. Today's violent sociopath is far more a than a failed cooperator.
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  • Age differences between mates in southern African pastoralists.Henry Harpending - 1992 - Behavioral and Brain Sciences 15 (1):102-103.
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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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  • On the brain and personality substrates of psychopathy.Jaak Panksepp, Brian Knutson & Laura Bird - 1995 - Behavioral and Brain Sciences 18 (3):568-570.
    Further understanding at neuroscientific and personality levels should considerably advance our ability to deal with individuals that have strong sociopathic tendencies. An analysis of neurodynamic responses to emotional stimuli will eventually be able to detect sociopathic tendencies of the brain. Such information could be used to enhance the options available to individuals at risk without limiting their personal freedoms.
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  • Vehicles all the way down?Nicholas S. Thompson - 1994 - Behavioral and Brain Sciences 17 (4):638-638.
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  • Taking vechicles seriously.David L. Hull - 1994 - Behavioral and Brain Sciences 17 (4):627-628.
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  • The consequences of group selection in a domain without genetic input: Culture.C. Loring Brace - 1994 - Behavioral and Brain Sciences 17 (4):611-612.
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  • Ambivalently held group-optimizing predispositions.Donald T. Campbell & John B. Gatewood - 1994 - Behavioral and Brain Sciences 17 (4):614-614.
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  • Fatherless rearing leads to sociopathy.David T. Lykken - 1995 - Behavioral and Brain Sciences 18 (3):563-564.
    Endorsing Mealey's analysis, it is pointed out that increasing rates of crime and violence are due to increasing proportions of children being reared in circumstances radically different from the extendedfamily environment to which we are evolntionarily adapted, that is, they are reared without fathers.
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  • A critique of R.d. Alexander's views on group selection.David Sloan Wilson - 1999 - Biology and Philosophy 14 (3):431-449.
    Group selection is increasingly being viewed as an important force in human evolution. This paper examines the views of R.D. Alexander, one of the most influential thinkers about human behavior from an evolutionary perspective, on the subject of group selection. Alexander's general conception of evolution is based on the gene-centered approach of G.C. Williams, but he has also emphasized a potential role for group selection in the evolution of individual genomes and in human evolution. Alexander's views are internally inconsistent and (...)
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  • On the adaptive value of some mate selection strategies.Klaus Jaffe - 1999 - Acta Biotheoretica 47 (1):29-40.
    Results of an agent-based computer simulation of the evolution of diploid sexual organisms showed that several mate selection strategies confer much higher average fitness to the simulated populations, and higher evolutionary stability to the alleles coding for these strategies, than random mating. Strategies which select for ''good genes'' were very successful, and so were strategies based on assortative mating. The results support the hypothesis that mating is not likely to be random in nature and that the most successful mate selection (...)
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  • Marital choice and reproductive strategies.Robert Schoen - 1992 - Behavioral and Brain Sciences 15 (1):109-109.
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  • The May-September algorithm meets the 20th century actuarial table.Gwen J. Broude - 1992 - Behavioral and Brain Sciences 15 (1):94-95.
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