Tandem androgenic and psychological shifts in male reproductive effort following a manipulated “win” or “loss” in a sporting competition

© 2018, The Author(s). Male-male competition is involved in inter- and intrasexual selection, with both endocrine and psychological factors presumably contributing to reproductive success in human males. We examined relationships among men’s naturally occurring testosterone, their self-perceived mate value (SPMV), self-esteem, sociosexuality, and expected likelihood of approaching attractive women versus situations leading to child involvement. We then monitored changes in these measures in male rowers (N = 38) from Cambridge, UK, following a manipulated “win” or “loss” as a result of an indoor rowing contest. Baseline results revealed that men with heightened testosterone and SPMV values typically had greater inclinations toward engaging in casual sexual relationships and a higher likelihood of approaching attractive women in a hypothetical social situation. As anticipated, both testosterone and SPMV increased following a manipulated “victory” and were associated with heightened sociosexuality, and increased expectations toward approaching attractive women versus individuals who would involve them in interacting with children after the race. SPMV and self-esteem appeared to mediate some of the effects of testosterone on post-race values. These findings are considered in the broader context of individual trade-offs between mating and parental effort and a model of the concurrent and dynamic androgenic and psychological influences contributing to male reproductive effort and success

Tandem androgenic and psychological shifts in male reproductive effort following a manipulated "win" or "loss" in a sporting competition

Male-male competition is involved in inter- and intrasexual selection, with both endocrine and psychological factors presumably contributing to reproductive success in human males. We examined relationships among men’s naturally occurring testosterone, their self-perceived mate value (SPMV), self-esteem, sociosexuality, and expected likelihood of approaching attractive women versus situations leading to child involvement. We then monitored changes in these measures in male rowers (N = 38) from Cambridge, UK, following a manipulated “win” or “loss” as a result of an indoor rowing contest. Baseline results revealed that men with heightened testosterone and SPMV values typically had greater inclinations toward engaging in casual sexual relationships and a higher likelihood of approaching attractive women in a hypothetical social situation. As anticipated, both testosterone and SPMV increased following a manipulated “victory” and were associated with heightened sociosexuality, and increased expectations toward approaching attractive women versus individuals who would involve them in interacting with children after the race. SPMV and self-esteem appeared to mediate some of the effects of testosterone on post-race values. These findings are considered in the broader context of individual trade-offs between mating and parental effort and a model of the concurrent and dynamic androgenic and psychological influences contributing to male reproductive effort and success

How willing are you to accept sexual requests from slightly unattractive to exceptionally attractive imagined requestors?

This is the post print version of the article. The official published version can be accessed from the link below.In their classic study of differences in mating strategies (Clark & Hatfield, 1989), men and women demonstrated a striking difference in interest in casual sex. The current study examined the role of requestor physical attractiveness (slightly unattractive, moderately attractive and exceptionally attractive) on men's and women's willingness to accept three different requests (go out, come to apartment, go to bed) in a questionnaire study. We tested two hypotheses, using a sample of 427 men and 443 women from three countries. Hypothesis 1 states that men, relative to women, will demonstrate a greater willingness to accept the “come to apartment” and “go to bed” requests but not the “go out” request for all three levels of requestor attractiveness. This hypothesis reflects Clark and Hatfield's (1989) main findings. Hypothesis 2 states that the physical attractiveness of a potential partner will have a greater effect on women's than on men's willingness to accept all three requests, and particularly for the explicit request for casual sex. The results partially supported Hypothesis 1 and fully supported Hypothesis 2. The discussion highlights limitations of the current research and presents directions for future research

Intergenerational conflicts may help explain parental absence effects on reproductive timing: a model of age at first birth in humans.

Background. Parental absences in childhood are often associated with accelerated reproductive maturity in humans. These results are counterintuitive for evolutionary social scientists because reductions in parental investment should be detrimental for offspring, but earlier reproduction is generally associated with higher fitness. In this paper we discuss a neglected hypothesis that early reproduction is often associated with parental absence because it decreases the average relatedness of a developing child to her future siblings. Family members often help each other reproduce, meaning that parents and offspring may find themselves in competition over reproductive opportunities. In these intergenerational negotiations offspring will have less incentive to help the remaining parent rear future half-siblings relative to beginning reproduction themselves. Method. We illustrate this "intergenerational conflict hypothesis" with a formal game-theoretic model. Results. We show that when resources constrain reproductive opportunities within the family, parents will generally win reproductive conflicts with their offspring, i.e., they will produce more children of their own and therefore delay existing offsprings' reproduction. This is due to the asymmetric relatedness between grandparents and grandchildren (r = .25), compared to siblings (r = 0.5), resulting in greater incentives for older siblings to help rear younger siblings than for grandparents to help rear grandchildren. However, if a parent loses or replaces their partner, the conflict between the parent and offspring becomes symmetric since half siblings are as related to one another as grandparents are to grandchildren. This means that the offspring stand to gain more from earlier reproduction when their remaining parent would produce half, rather than full, siblings. We further show that if parents senesce in a way that decreases the quality of their infant relative to their offspring's infant, the intergenerational conflict can shift to favor the younger generation

Evolutionary Psychology and Mental Health

AN EVOLUTIONARY PERSPECTIVE revolutionized our understanding of behavior over a generation ago, but most mental health clinicians and researchers still view evolution as an interesting or even threatening alternative, instead of recognizing it as an essential basic science for understanding mental disorders. Many factors explain this lag in incorporating new knowledge, but the most important may be the clinician’s pragmatic focus on finding ways to help people now. Evolutionary researchers have not found a new treatment for a single mental disorder, so why should mental health clinicians and researchers care about evolutionary psychology (EP)? This chapter attempts to answer that question. The greatest value of an evolutionary approach is not some specific find- ing or new therapy, but is instead the framework it provides for uniting all aspects of a biopsychosocial model. Perhaps equally valuable is the deeper empathy fostered by an evolutionary perspective on life’s vicissitudes. An evolutionary perspective does not compete with other theories that try to explain why some people have mental disorders and others do not. Instead, it asks a fundamentally differ- ent question: Why has natural selection left all humans so vulnerable to mental disorders? At first, the question seems senseless. Natural selection shapes mecha- nisms that work, so how can it help us understand why the mind fails? It is also difficult to see how it is useful to know why we are vulnerable. Who cares why all humans are vulnerable to depression, when the goal is to help the individual who is depressed here and now? Surmounting these conceptual hurdles is a challenge that requires time and effort. Researchers and clinicians will make the effort when they know what evolution offers to the understanding of mental disorders.Peer Reviewedhttps://deepblue.lib.umich.edu/bitstream/2027.42/145726/1/Nesse - 2015 - Evolutionary Psychology and Mental Health.pdfDescription of Nesse - 2015 - Evolutionary Psychology and Mental Health.pdf : Chapte

Mate Value and Self-Esteem: Evidence from Eight Cultural Groups

This paper explores self-perceived mate value (SPMV), and its association with self-esteem, in eight cultures. 1066 participants, from 8 cultural groups in 7 countries, rated themselves on 24 SPMVs and completed a measure of self-esteem. Consistent with evolutionary theory, women were more likely to emphasise their caring and passionate romantic nature. In line with previous cross-cultural research, characteristics indicating passion and romance and social attractiveness were stressed more by respondents from individualistic cultures, and those higher on self-expression (rather than survival) values; characteristics indicative of maturity and confidence were more likely to be mentioned by those from Traditional, rather than Secular, cultures. Contrary to gender role theory, societal equality had only limited interactions with sex and SPMV, with honesty of greater significance for male self-esteem in societies with unequal gender roles. These results point to the importance of cultural and environmental factors in influencing self-perceived mate qualities, and are discussed in relation to broader debates about the impact of gender role equality on sex differences in personality and mating strategies

Childhood adversity, attachment security, and adult relationships: A preliminary study

Several evolutionary theorists have linked early rearing context to later reproductive strategy, hypothesizing that strategies differentiate during development as functional responses to ecological characteristics, by individuals or through parental manipulation. Attachment security has been proposed as a mediator. In this study, 40 young adults were given a multidimensional assessment, including the Hazen and Shaver Adult Attachment Questionnaire. Twenty-four subjects were classified as having secure attachment styles, 16 as nonsecure. The magnitude and predictability of parental investment during childhood was classified as lower if there was a brief intersibling interval, parental divorce, fewer economic resources, or less nurturing parents (i.e., more childhood adversity). Several such indicators were present for 17 people, 12 of whom were nonsecure, compared to only 4 of the 23 others. The nonsecurely attached subjects were less likely to have attained enduring marriages. The 6/16 nonsecure who had a marriage or cohabitation began them at a younger age and after a shorter courtship period than did the 15/24 secure with such relationships. Separations or divorces had already occurred in the relationships of 4/6 nonsecure versus 5/15 secure. Attachment security was associated with childhood adversity and adult relationships for both men and women, when analyzed separately. A retrospective study cannot address cause and effect, because poor adult relationship outcomes might bias recall of parental behavior. However, results are consistent with theories that unpredictable early environments foster short-term rather than long-term mating strategies, possibly through affecting attachment styles.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/31362/1/0000274.pd

Addressing our inner salmon in an evolutionary framework for psychopathology

Life history theory is an elegant instrument for describing major differences in patterns of life history traits across plant and animal taxa (Charnov, 1993; Roff, 1992, 2002; Stearns, 1992). Typical life history traits discussed in the classic evolutionary biology literature include size at birth, growth pattern, age of sexual maturation, size at maturity, age of first reproduction, number and sex ratio of offspring produced, age and size-specific reproductive investments, age and size-specific mortality schedules, and length of lifespan (see Stearns, 1992). A basic assumption of the classic optimality approach to life history theory is that, given adequate genetic variation, the evolution of species has involved natural selection of optimal combinations of these traits. However, genetic and other constraints, and trade-offs have reduced the set of possible combinations. Life history theory predicts trade-offs between energetic investment in growth, maintenance, and reproduction across species, of which a trade-off between the main constituents of reproductive investment, mating and parental effort, may be the most common (McGlothlin, Jawor, & Ketterson, 2007). It is easy to see how if organisms possess finite resources that trade-offs affecting life history traits would necessarily evolve over evolutionary time. If the “pie of finite resources” is divided up between life history traits, taking a large slice of one type of trait leaves less of the pie to be divided into other forms of investment. Among vertebrate species, for example, salmon have very different life histories than primate species. Their life history consists of relatively rapid growth, early maturation and first reproduction, small size, little parental care, and the production of a high number of offspring, followed immediately by death in semelparous species,eclipsing a postreproductive period. In contrast, the life history of human beings consists of relatively slow development, late puberty and first reproduction, iteroparity, large body size, low number of offspring, followed by high parental investment (extended to grandparental investment) and a long life span, including a female postreproductive period