scholarly journals A Cascade Model of Sociodevelopmental Events Leading to Men's Perpetration of Violence Against Female Romantic Partners

2021 ◽  
Vol 19 (4) ◽  
pp. 147470492110407
Author(s):  
Farnaz Kaighobadi ◽  
Aurelio J. Figueredo ◽  
Todd K. Shackelford ◽  
David F. Bjorklund
Keyword(s):  
Life History ◽  
Romantic Relationship ◽  
Life History Theory ◽  
Self Regulation ◽  
Romantic Partners ◽  
Cascade Model ◽  
Life History Strategies ◽  
Parental Effort ◽  
Childhood Experiences ◽  
Mate Retention

Conceptually driven by life history theory, the current study investigated a hypothesized hierarchy of behaviors leading to men's perpetration of violence in intimate relationships. Using a series of hierarchical regressions, we tested a causal cascade model on data provided by 114 men in a committed romantic relationship. The results supported the hypothesized hierarchy of sociodevelopmental events: (1) men's childhood experiences with their parents’ parental effort predicted men's life history strategies; (2) men's life history strategies predicted men's behavioral self-regulation; (3) men's self-regulation predicted men's perceptions of partner infidelity risk; (4) perceptions of infidelity risk predicted men's frequency of engagement in nonviolent mate retention behaviors; (5) men's mate retention behaviors predicted men's frequency of partner-directed violence. The overall cascade model explained 36% of variance in men's partner-directed violence.

scholarly journals Love Styles in the Context of Life History Theory

2017 ◽  
Vol 48 (2) ◽  
pp. 237-249
Author(s):  
Magdalena Marzec ◽  
Andrzej Łukasik
Keyword(s):  
Life History ◽  
Reproductive Strategies ◽  
Life History Theory ◽  
Mating Effort ◽  
Parental Effort ◽  
Short Term ◽  
Childhood Experiences ◽  
Love Styles ◽  
Number Of Children

Abstract The evolutionary function of love is to create a strong bond between the partners with reproduction in view. In order to achieve this goal, humans use various sexual/reproductive strategies, which have evolved due to specific reproductive benefits. The use of particular strategies depends on many factors but one of the most important is early childhood experiences, on which life history theory (LHT) focuses. John Lee (1973) identified 6 basic love styles: eros, ludus, storge, pragma, agape, and mania. Our goal was to check whether love styles may be treated as sexual/reproductive strategies in the context of LHT - slow or fast strategy. In our study (N = 177) we found that people who prefer the slow reproductive strategy are inclined to show passionate, pragmatic and friendly love, and those who prefer the fast strategy, treated love as a game. A low level of environmental stress in childhood results in preferring eros, storge and agape love styles, belonging to the slow strategy, and a high one results in preferring ludus, which belongs to the fast strategy. People representing eros, storge or pragma styles have restricted sociosexual orientation so they prefer long-term relationships, whereas those with the ludus style are people with unrestricted orientation, preferring short-term relationships. Besides, storge, agape and pragma seem to determine preferring qualities connected with parental effort in one’s partner, mania - with mating effort, and eros - with both kinds of effort. No correlation was found between the love style and the number of children.

Sexual size dimorphism and life history traits in an island-mainland system: an overview of the lizard genus Microlophus

2021 ◽  
pp. 1-7
Author(s):  
Ken S. Toyama ◽  
Christopher K. Boccia
Keyword(s):  
Life History ◽  
South America ◽  
Life History Theory ◽  
Life History Traits ◽  
Sexual Size Dimorphism ◽  
Life History Strategies ◽  
Galápagos Islands ◽  
Size Dimorphism ◽  
Rensch's Rule ◽  
Comprehensive Compilation

Abstract Opposing life history strategies are a common result of the different ecological settings experienced by insular and continental species. Here we present a comprehensive compilation of data on sexual size dimorphism (SSD) and life history traits of Microlophus, a genus of lizards distributed in western South America and the Galápagos Islands, and test for differences between insular and continental species under life history theory expectations. Contrary to our predictions, we found no differences in SSD between localities or evidence that Microlophus follows Rensch’s rule. However, as expected, head dimensions and maturity sizes were significantly larger in insular species while continental species had larger clutches. Our results show that Microlophus exhibits some of the patterns expected from an island-mainland system, but unexplained patterns will only be resolved through future ecological, morphological and behavioural studies integrating both faunas.

Personality disorders

2015 ◽  
pp. 277-294
Author(s):  
Martin Brüne
Keyword(s):  
Early Childhood ◽  
Life History ◽  
Personality Traits ◽  
Personality Disorders ◽  
Resource Availability ◽  
Life History Strategies ◽  
Subjective Distress ◽  
Childhood Experiences ◽  
Dependence Versus ◽  
Behavioural Patterns

Personality disorders (PD) concern inflexible and maladaptive cognitive, emotional, and behavioural patterns, which cause significant functional impairment or subjective distress. One group of PD is characterized by ‘eccentricity’, another by ‘dramatic’ behaviour, and a third cluster by predominant anxiety. Personality traits reflect individual patterns of behaviour that serve the purpose to achieve important biosocial goals. These behaviours can be grouped according to their interpersonal meaning: dominance versus submission; competition versus cooperation; dependence versus nurturance; assertion versus avoidance; aggression versus defence; and risk-taking versus harm avoidance. From a life-history perspective, personality traits, as well as personality disorders representing the extremes of variation of normal trait distribution, can be differentiated into ‘fast’ and ‘slow’ life-history strategies. Predictions about future resource availability arise from early childhood experiences with caregivers and the interaction of these experiences with genes involved in the regulation of aggression, attachment, etc.

Life History Strategies

2018 ◽  
pp. 95-126
Author(s):  
Marco Del Giudice
Keyword(s):  
Life History ◽  
Individual Differences ◽  
Life History Theory ◽  
Human Life ◽  
Life History Strategy ◽  
Current Theory ◽  
Life History Strategies ◽  
Extended Model ◽  
Life History Variation ◽  
Basic Model

The chapter introduces the basics of life history theory, the concept of life history strategy, and the fast–slow continuum of variation. After reviewing applications to animal behavior and physiology, the chapter reviews current theory and evidence on individual differences in humans as manifestations of alternative life history strategies. The chapter first presents a “basic model” of human life history–related traits, then advances an “extended model” that identifies multiple cognitive-behavioral profiles within fast and slow strategies. Specifically, it is proposed that slow strategies comprise prosocial/caregiving and skilled/provisioning profiles, whereas fast strategies comprise antisocial/exploitative and seductive/creative profiles. The chapter also reviews potential neurobiological markers of life history variation and considers key methodological issues in this area.

scholarly journals Cuckoos, cowbirds and hosts: adaptations, trade-offs and constraints

2006 ◽  
Vol 362 (1486) ◽  
pp. 1873-1886 ◽  
Author(s):  
Oliver Krüger
Keyword(s):  
Life History ◽  
Brood Parasitism ◽  
Reproductive Strategies ◽  
Life History Theory ◽  
Model Systems ◽  
Life History Strategies ◽  
Host System ◽  
Brood Parasites ◽  
Trade Offs ◽  
Evolution Of Life

The interactions between brood parasitic birds and their host species provide one of the best model systems for coevolution. Despite being intensively studied, the parasite–host system provides ample opportunities to test new predictions from both coevolutionary theory as well as life-history theory in general. I identify four main areas that might be especially fruitful: cuckoo female gentes as alternative reproductive strategies, non-random and nonlinear risks of brood parasitism for host individuals, host parental quality and targeted brood parasitism, and differences and similarities between predation risk and parasitism risk. Rather than being a rare and intriguing system to study coevolutionary processes, I believe that avian brood parasites and their hosts are much more important as extreme cases in the evolution of life-history strategies. They provide unique examples of trade-offs and situations where constraints are either completely removed or particularly severe.

scholarly journals The effects of age at menarche and first sexual intercourse on reproductive and behavioural outcomes: a Mendelian randomization study

2018 ◽  
Author(s):  
Rebecca B Lawn ◽  
Hannah M Sallis ◽  
Robyn E Wootton ◽  
Amy E Taylor ◽  
Perline Demange ◽  
...  
Keyword(s):  
Life History ◽  
Sexual Intercourse ◽  
Life History Theory ◽  
Mendelian Randomization ◽  
Causal Effect ◽  
Life History Strategies ◽  
Age At Menarche ◽  
Age At First Birth ◽  
Risky Behaviour ◽  
First Sexual Intercourse

SummaryThere is substantial variation in the timing of significant reproductive life events such as menarche and first sexual intercourse. Life history theory explains this variation as an adaptive response to the developmental environment. In environments characterized by harsh conditions, adopting a fast life history strategy may increase fitness. In line with this, there is evidence demonstrating that greater childhood adversity is associated with earlier age at menarche. Here we applied Mendelian randomization (MR) methods to investigate whether there is a causal effect of variation in age at menarche and age at first sexual intercourse on outcomes related to reproduction, education and risky behaviour in UK Biobank (N = 114883–181,255). Our results suggest that earlier age at menarche affects some traits that characterize life history strategies including earlier age at first and last birth, decreased educational attainment, and decreased age at leaving education (for example, we found evidence for a 0.26 year decrease in age at first birth per year decrease in age at menarche, 95% confidence interval: −0.34 to −0.17; p < 0.0001). We find no clear evidence of effects of age at menarche on other outcomes, such as risk taking behaviour. Age at first sexual intercourse was also related to many life history outcomes, although there was evidence of horizontal pleiotropy which violates an assumption of MR and results should be treated with caution. Taken together, these results highlight how MR can be applied to test predictions of life history theory and to better understand determinants of health and social behaviour.

scholarly journals Differential reproductive responses to stress reveal the role of life-history strategies within a species

2013 ◽  
Vol 280 (1771) ◽  
pp. 20132090 ◽  
Author(s):  
J. Schultner ◽  
A. S. Kitaysky ◽  
G. W. Gabrielsen ◽  
S. A. Hatch ◽  
C. Bech
Keyword(s):  
Life History ◽  
Life History Theory ◽  
Life History Strategies ◽  
Short Term ◽  
Food Shortages ◽  
Investment In Reproduction ◽  
Response To Stress ◽  
Environmental Events ◽  
Two Populations

Life-history strategies describe that ‘slow’- in contrast to ‘fast’-living species allocate resources cautiously towards reproduction to enhance survival. Recent evidence suggests that variation in strategies exists not only among species but also among populations of the same species. Here, we examined the effect of experimentally induced stress on resource allocation of breeding seabirds in two populations with contrasting life-history strategies: slow-living Pacific and fast-living Atlantic black-legged kittiwakes. We tested the hypothesis that reproductive responses in kittiwakes under stress reflect their life-history strategies. We predicted that in response to stress, Pacific kittiwakes reduce investment in reproduction compared with Atlantic kittiwakes. We exposed chick-rearing kittiwakes to a short-term (3-day) period of increased exogenous corticosterone (CORT), a hormone that is released during food shortages. We examined changes in baseline CORT levels, parental care and effects on offspring. We found that kittiwakes from the two populations invested differently in offspring when facing stress. In response to elevated CORT, Pacific kittiwakes reduced nest attendance and deserted offspring more readily than Atlantic kittiwakes. We observed lower chick growth, a higher stress response in offspring and lower reproductive success in response to CORT implantation in Pacific kittiwakes, whereas the opposite occurred in the Atlantic. Our findings support the hypothesis that life-history strategies predict short-term responses of individuals to stress within a species. We conclude that behaviour and physiology under stress are consistent with trade-off priorities as predicted by life-history theory. We encourage future studies to consider the pivotal role of life-history strategies when interpreting inter-population differences of animal responses to stressful environmental events.

scholarly journals Life-history traits and description of the new gonochoric amphimictic Mesobiotus joenssoni (Eutardigrada: Macrobiotidae) from the island of Elba, Italy

2019 ◽  
Author(s):  
Roberto Guidetti ◽  
Elisa Gneuß ◽  
Michele Cesari ◽  
Tiziana Altiero ◽  
Ralph O Schill
Keyword(s):  
Life History ◽  
Life History Theory ◽  
Life History Traits ◽  
Life Cycles ◽  
Life History Strategies ◽  
Egg Hatching ◽  
Body Segments ◽  
Hatching Time ◽  
Laboratory Cultures ◽  
The Mean

Abstract Comparative analyses of life-history theory studies are based on the characteristics of the life cycles of different species. For tardigrades, life-history traits are available only from laboratory cultures, most of which have involved parthenogenetic species. The discovery of a new gonochoristic bisexual Mesobiotus species in a moss collected on the island of Elba (Italy) provides us with the opportunity to describe Mesobiotus joenssoni sp. nov. and to collect data on the life-history traits of cultured specimens to increase our knowledge of the life-history strategies present in tardigrades. This new species is differentiated from all other species of the genus by the presence of granules (~1 µm in diameter) on the dorsal cuticle of the last two body segments, two large bulges (gibbosities) on the hindlegs and long, conical egg processes. The species exhibits sexual dimorphism in body length, with females being longer than males of the same age. The mean lifespan of specimens was 86 days, with a maximum of 150 days. The mean age at first oviposition was 19.8 days and the mean egg hatching time 15.4 days. The life-cycle traits correspond to those collected for the only other two macrobiotid species with gonochoric amphimictic reproduction examined so far.

scholarly journals Ecology-driven stereotypes override race stereotypes

2015 ◽  
Vol 113 (2) ◽  
pp. 310-315 ◽  
Author(s):  
Keelah E. G. Williams ◽  
Oliver Sng ◽  
Steven L. Neuberg
Keyword(s):  
United States ◽  
Life History ◽  
Life History Theory ◽  
The United States ◽  
Life History Strategies ◽  
Racial Groups ◽  
Black And White ◽  
Lay Understanding ◽  
Per Se ◽  
Rule Out

Why do race stereotypes take the forms they do? Life history theory posits that features of the ecology shape individuals’ behavior. Harsh and unpredictable (“desperate”) ecologies induce fast strategy behaviors such as impulsivity, whereas resource-sufficient and predictable (“hopeful”) ecologies induce slow strategy behaviors such as future focus. We suggest that individuals possess a lay understanding of ecology’s influence on behavior, resulting in ecology-driven stereotypes. Importantly, because race is confounded with ecology in the United States, we propose that Americans’ stereotypes about racial groups actually reflect stereotypes about these groups’ presumed home ecologies. Study 1 demonstrates that individuals hold ecology stereotypes, stereotyping people from desperate ecologies as possessing faster life history strategies than people from hopeful ecologies. Studies 2–4 rule out alternative explanations for those findings. Study 5, which independently manipulates race and ecology information, demonstrates that when provided with information about a person’s race (but not ecology), individuals’ inferences about blacks track stereotypes of people from desperate ecologies, and individuals’ inferences about whites track stereotypes of people from hopeful ecologies. However, when provided with information about both the race and ecology of others, individuals’ inferences reflect the targets’ ecology rather than their race: black and white targets from desperate ecologies are stereotyped as equally fast life history strategists, whereas black and white targets from hopeful ecologies are stereotyped as equally slow life history strategists. These findings suggest that the content of several predominant race stereotypes may not reflect race, per se, but rather inferences about how one’s ecology influences behavior.

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