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  1. The Nature of Race: the Genealogy of the Concept and the Biological Construct’s Contemporaneous Utility.John Fuerst - 2015 - Open Behavioral Genetics.
    Racial constructionists, anti-naturalists, and anti-realists have challenged users of the biological race concept to provide and defend, from the perspective of biology, biological philosophy, and ethics, a biologically informed concept of race. In this paper, an ontoepistemology of biology is developed. What it is, by this, to be "biological real" and "biologically meaningful" and to represent a "biological natural division" is explained. Early 18th century race concepts are discussed in detail and are shown to be both sensible and not greatly (...)
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  • Biological versus social psychological bases of mate selection.George Levinger & Lee A. Kirkpatrick - 1992 - Behavioral and Brain Sciences 15 (1):103-104.
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  • Age similarity is genetic similarity.J. Philippe Rushton - 1992 - Behavioral and Brain Sciences 15 (1):108-108.
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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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  • An explanatory mechanism that merits more attention.Nancy Eisenberg - 1991 - Behavioral and Brain Sciences 14 (4):749-749.
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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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  • Ethnic nepotism in science?J. Philippe Rushton - 1991 - Behavioral and Brain Sciences 14 (3):526-527.
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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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  • 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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  • 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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  • 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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  • 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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  • 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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  • 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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  • Mate choice turns cognitive.Geoffrey F. Miller & Peter M. Todd - 1998 - Trends in Cognitive Sciences 2 (5):190-198.
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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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  • 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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  • 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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  • Hominids, coalitions, and weapons: Not vehicles.Jim Moore - 1994 - Behavioral and Brain Sciences 17 (4):632-632.
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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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  • Culture, biology, and human behavior.Horst D. Steklis & Alex Walter - 1991 - Human Nature 2 (2):137-169.
    Social scientists have not integrated relevant knowledge from the biological sciences into their explanations of human behavior. This failure is due to a longstanding antireductionistic bias against the natural sciences, which follows on a commitment to the view that social facts must be explained by social laws. This belief has led many social scientists into the error of reifying abstract analytical constructs into entities that possess powers of agency. It has also led to a false nature-culture dichotomy that effectively undermines (...)
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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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  • “Just So” stories and sociopathy.Andrew Futterman & Garland E. Allen - 1995 - Behavioral and Brain Sciences 18 (3):557-558.
    Sociobiological explanation requires both a reliable and a valid definition of the sociopathy phenotype. Mealey assumes that such reliable and valid definition of sociopathy exists in her A review of psychiatric literature on the diagnosis of antisocial personality disorder clearly demonstrates that this assumption is faulty. There is substantial disagreement among diagnostic systems (e.g., RDC, DSM-III) over what constitutes the antisocial phenotype, different systems identify different individuals as sociopathic. Without a valid definition of sociopathy, sociobiological theories like Mealey's should be (...)
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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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  • 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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  • 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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  • 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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  • On building bridges between social psychology and evolutionary biology.Richard Lippa - 1992 - Behavioral and Brain Sciences 15 (1):104-105.
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  • Wanting and getting ain't the same.Pierre L. van den Berghe - 1992 - Behavioral and Brain Sciences 15 (1):116-117.
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  • Some philosophical implications of the rehabilitation of group selection.John Dupré - 1994 - Behavioral and Brain Sciences 17 (4):619-620.
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  • Group selection and the group mind in science.Gordon M. Burghardt - 1994 - Behavioral and Brain Sciences 17 (4):613-613.
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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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  • 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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  • The role of attachment in the development and prevention of sociopathy.Marinus H. Van IJzendoorn - 1995 - Behavioral and Brain Sciences 18 (3):576-577.
    Mealey's sociobiological model of sociopathy could profit from attachment theory, in particular, the theory and research on the basis of the Adult Attachment Interview (Main & Goldwyn 1985–1993). Findings of an adult attachment study in a forensic psychiatric setting are summarized. Three attachment-oriented strategies for families, schools, and forensic settings are proposed to help reduce or prevent secondary sociopathy and criminal recidivism.
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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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  • Romantic love and sexual desire.Aaron Ben-Ze'ev - 1997 - Philosophia 25 (1-4):3-32.
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  • Is sociopathy a type or not? Will the “real” sociopathy please stand up?James Snyder - 1995 - Behavioral and Brain Sciences 18 (3):575-576.
    The validity of the classification of “primary sociopaths” as a qualitatively distinct group in the general population is questioned. Cenetic variation in the experience and expression of emotions may play a role in the development of antisocial behavior. However, research clearly documents that socialization environments powerfully modify the expression of genetic biases in a manner that increases or decreases the risk for “sociopathy.”.
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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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  • In praise of replicators.James F. Crow - 1994 - Behavioral and Brain Sciences 17 (4):616-616.
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  • Assortative Pairing and Life History Strategy.Aurelio José Figueredo & Pedro S. A. Wolf - 2009 - Human Nature 20 (3):317-330.
    A secondary analysis was performed on preliminary data from an ongoing cross-cultural study on assortative pairing. Independently sampled pairs of opposite-sex romantic partners and of same-sex friends rated themselves and each other on Life History (LH) strategy and mate value. Data were collected in local bars, clubs, coffeehouses, and other public places from three different cultures: Tucson, Arizona; Hermosillo, Sonora; and San José, Costa Rica. The present analysis found that slow LH individuals assortatively pair with both sexual and social partners (...)
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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 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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  • 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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  • 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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  • 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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  • On the separation of reproduction from mating preferences.Betty M. Bayer - 1992 - Behavioral and Brain Sciences 15 (1):92-93.
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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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  • 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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