Corrigendum to “Life history strategies and procrastination: The role of environmental unpredictability” [Personality and Individual Differences 117 (2017) 23–29]

2018 ◽  
Vol 132 ◽  
pp. 134
Author(s):  
Bin-Bin Chen ◽  
Wenxiang Qu
Author(s):  
Marco Del Giudice

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.


2020 ◽  
Vol 37 (8-9) ◽  
pp. 2438-2458
Author(s):  
Ohad Szepsenwol

Recent extensions to life history theory posit that exposure to environmental unpredictability during childhood should forecast negative parental behaviors in adulthood. In the current research, this logic was extended to co-parental behaviors, which refer to how parents coordinate, share responsibility, and support each other’s parental efforts. The effects of early-life unpredictability on individual and dyadic co-parental functioning were examined in a sample of 109 families (two parents and their firstborn child) who were followed longitudinally from before the child’s birth until the age of two. Greater early-life unpredictability (family changes, residential changes, and parents’ occupational changes by age 8) experienced by mothers, but not fathers, predicted more negative co-parental behaviors in triadic observations 6 months post birth, and lower couple-reported co-parenting quality assessed 3, 9, 18, and 24 months post birth. These effects were not explained by parents’ childhood socioeconomic status or current relationship quality. These findings highlight the role of mothers in shaping co-parenting relationships and how these relationships might be influenced by mothers’ early-life experiences.


2017 ◽  
Vol 87 ◽  
pp. 164-175 ◽  
Author(s):  
Lee T. Gettler ◽  
Calen P. Ryan ◽  
Dan T.A. Eisenberg ◽  
Margarita Rzhetskaya ◽  
M. Geoffrey Hayes ◽  
...  

2012 ◽  
Vol 48 (3) ◽  
pp. 722-739 ◽  
Author(s):  
Frederick X. Gibbons ◽  
Megan E. Roberts ◽  
Meg Gerrard ◽  
Zhigang Li ◽  
Steven R. H. Beach ◽  
...  

2013 ◽  
Vol 280 (1771) ◽  
pp. 20132090 ◽  
Author(s):  
J. Schultner ◽  
A. S. Kitaysky ◽  
G. W. Gabrielsen ◽  
S. A. Hatch ◽  
C. Bech

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.


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