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

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.

2018 ◽  
Author(s):  
Iris Wang ◽  
Nicholas Michael Michalak ◽  
Joshua Ackerman

Life history theory posits organisms face tradeoffs in how they allocate resources to reproduction, parenting, and growth. These patterns of resource allocation can be classified more broadly into life history strategies, which vary on a continuum from fast to slow. These distinctions can be applied to describe within species and between species differences. Slow strategies are marked by increased investment in growth, a delay in reproductive investment, and increased investment in parenting. In contrast, fast strategies are marked by early investment in reproduction at a cost of growth and a reduced investment in parenting in favor of further reproduction.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
David Canal ◽  
Francisco Garcia-Gonzalez ◽  
László Zsolt Garamszegi

AbstractThe trade-off between current and future reproduction is a cornerstone of life history theory, but the role of within-individual plasticity on life history decisions and its connections with overall fitness and behaviour remains largely unknown. By manipulating available resources for oviposition at the beginning of the reproductive period, we experimentally constrained individual life history trajectories to take different routes in a laboratory study system, the beetle Callosobruchus maculatus, and investigated its causal effects on fecundity, survival and behaviour. Compared to females without resource limitations, females experiencing restricted conditions for oviposition had reduced fecundity early in life but increased fecundity when resources became plentiful (relative to both the previous phase and the control group) at the expense of longevity. Constrained reproduction in early life also affected behaviour, as movement activity changed differently in the two experimental groups. Experiencing reproductive constraints has, therefore, consequences for future reproduction investments and behaviour, which may lead individuals to follow different life history strategies.


2008 ◽  
Vol 29 (2) ◽  
pp. 245-256 ◽  
Author(s):  
Carissa Jones ◽  
Isaac Rojas-González ◽  
Julio Lemos-Espinal ◽  
Jaime Zúñiga-Vega

Abstract There appears to be variation in life-history strategies even between populations of the same species. For ectothermic organisms such as lizards, it has been predicted that demographic and life-history traits should differ consistently between temperate and tropical populations. This study compares the demographic strategies of a temperate and a tropical population of the lizard Xenosaurus platyceps. Population growth rates in both types of environments indicated populations in numerical equilibrium. Of the two populations, we found that the temperate population experiences lower adult mortality. The relative importance (estimated as the relative contribution to population growth rate) of permanence and of the adult/reproductive size classes is higher in the temperate population. In contrast, the relative importance for average fitness of fecundity and growth is higher in the tropical population. These results are consistent with the theoretical frameworks about life-historical differences among tropical and temperate lizard populations.


2021 ◽  
pp. 1-7
Author(s):  
Ken S. Toyama ◽  
Christopher K. Boccia

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.


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.


2020 ◽  
Vol 16 (2) ◽  
pp. 20190707
Author(s):  
Joanie Van de Walle ◽  
Andreas Zedrosser ◽  
Jon E. Swenson ◽  
Fanie Pelletier

Life-history theory predicts a trade-off between offspring size and number. However, the role of intra-litter phenotypic variation in shaping this trade-off is often disregarded. We compared the strength of the relationship between litter size and mass from the perspective of the lightest and the heaviest yearling offspring in 110 brown bear litters in Sweden. We showed that the mass of the lightest yearlings decreased with increasing litter size, but that the mass of the heaviest yearling remained stable, regardless of litter size. Consistent with a conservative reproductive strategy, our results suggest that mothers maintained a stable investment in a fraction of the litter, while transferring the costs of larger litter size to the remaining offspring. Ignoring intra-litter phenotypic variation may obscure our ability to detect a trade-off between offspring size and number.


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

2006 ◽  
Vol 362 (1486) ◽  
pp. 1873-1886 ◽  
Author(s):  
Oliver Krüger

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.


2013 ◽  
Vol 26 (1) ◽  
pp. 1-20 ◽  
Author(s):  
Bruce J. Ellis ◽  
Marco Del Giudice

AbstractHow do exposures to stress affect biobehavioral development and, through it, psychiatric and biomedical disorder? In the health sciences, the allostatic load model provides a widely accepted answer to this question: stress responses, while essential for survival, have negative long-term effects that promote illness. Thus, the benefits of mounting repeated biological responses to threat are traded off against costs to mental and physical health. The adaptive calibration model, an evolutionary–developmental theory of stress–health relations, extends this logic by conceptualizing these trade-offs as decision nodes in allocation of resources. Each decision node influences the next in a chain of resource allocations that become instantiated in the regulatory parameters of stress response systems. Over development, these parameters filter and embed information about key dimensions of environmental stress and support, mediating the organism's openness to environmental inputs, and function to regulate life history strategies to match those dimensions. Drawing on the adaptive calibration model, we propose that consideration of biological fitness trade-offs, as delineated by life history theory, is needed to more fully explain the complex relations between developmental exposures to stress, stress responsivity, behavioral strategies, and health. We conclude that the adaptive calibration model and allostatic load model are only partially complementary and, in some cases, support different approaches to intervention. In the long run, the field may be better served by a model informed by life history theory that addresses the adaptive role of stress response systems in regulating alternative developmental pathways.


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