scholarly journals Life history trade-offs and the partitioning of maternal investment

2018 ◽  
Vol 2018 (1) ◽  
pp. 153-166 ◽  
Author(s):  
Jonathan C K Wells
2021 ◽  
Author(s):  
◽  
John Van der Sman

<p>Parental investment per offspring is a key life history trait in which offspring size and number combinations are balanced in order to maximise fitness. When food is scarce and energy for reproduction is reduced, changes in reproductive allocation can be expected. These adjustments may go on to influence the growth and survival of the next generation. Trade-offs in reproductive allocation in response to food availability occurred differently in each of the three whelks species of this study. However, each species traded numbers of offspring rather than size of offspring when fed low food. Offspring size was more variable among and within capsules than among food treatments. Capsule size was a plastic trait that varied in response to food treatments in each of the species and varied among populations of the same species. Carry-over effects of maternal nutrition influenced juvenile growth in all three species. However, while juvenile growth was greater when adults were fed high food in two of the species, high adult food suppressed the growth of juveniles of the third species. This may be a mechanism to prevent potential negative consequences of rapid growth. There was no evidence of a maternal effect of mortality in any of the three species. Greater variation in hatchling size occurred in the species in which nurse egg feeding occurred. Nurse egg feeding may be a successful strategy in unpredictable environments where optimal offspring size changes from year to year. Regional differences in reproductive allocation between whelks separated by small distances suggest that populations may be isolated from one another and may need to be managed separately for conservation purposes. This study highlights the influence of maternal nutritional effects on life history and the potential impacts that these may have on population and community structure.</p>


2021 ◽  
Author(s):  
◽  
John Van der Sman

<p>Parental investment per offspring is a key life history trait in which offspring size and number combinations are balanced in order to maximise fitness. When food is scarce and energy for reproduction is reduced, changes in reproductive allocation can be expected. These adjustments may go on to influence the growth and survival of the next generation. Trade-offs in reproductive allocation in response to food availability occurred differently in each of the three whelks species of this study. However, each species traded numbers of offspring rather than size of offspring when fed low food. Offspring size was more variable among and within capsules than among food treatments. Capsule size was a plastic trait that varied in response to food treatments in each of the species and varied among populations of the same species. Carry-over effects of maternal nutrition influenced juvenile growth in all three species. However, while juvenile growth was greater when adults were fed high food in two of the species, high adult food suppressed the growth of juveniles of the third species. This may be a mechanism to prevent potential negative consequences of rapid growth. There was no evidence of a maternal effect of mortality in any of the three species. Greater variation in hatchling size occurred in the species in which nurse egg feeding occurred. Nurse egg feeding may be a successful strategy in unpredictable environments where optimal offspring size changes from year to year. Regional differences in reproductive allocation between whelks separated by small distances suggest that populations may be isolated from one another and may need to be managed separately for conservation purposes. This study highlights the influence of maternal nutritional effects on life history and the potential impacts that these may have on population and community structure.</p>


2019 ◽  
Author(s):  
Gretchen F. Wagner ◽  
Emeline Mourocq ◽  
Michael Griesser

Biparental care systems are a valuable model to examine conflict, cooperation, and coordination between unrelated individuals, as the product of the interactions between the parents influences the fitness of both individuals. A common experimental technique for testing coordinated responses to changes in the costs of parental care is to temporarily handicap one parent, inducing a higher cost of providing care. However, dissimilarity in experimental designs of these studies has hindered interspecific comparisons of the patterns of cost distribution between parents and offspring. Here we apply a comparative experimental approach by handicapping a parent at nests of five bird species using the same experimental treatment. In some species, a decrease in care by a handicapped parent was compensated by its partner, while in others the increased costs of care were shunted to the offspring. Parental responses to an increased cost of care primarily depended on the total duration of care that offspring require. However, life history pace (i.e., adult survival and fecundity) did not influence parental decisions when faced with a higher cost of caring. Our study highlights that a greater attention to intergenerational trade-offs is warranted, particularly in species with a large burden of parental care. Moreover, we demonstrate that parental care decisions may be weighed more against physiological workload constraints than against future prospects of reproduction, supporting evidence that avian species may devote comparable amounts of energy into survival, regardless of life history strategy.


2017 ◽  
Vol 49 (6) ◽  
pp. 783 ◽  
Author(s):  
Yan WANG ◽  
Zhenchao LIN ◽  
Bowen HOU ◽  
Shijin SUN

Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle

Hormones mediate the expression of life history traits—phenotypic traits that contribute to lifetime fitness (i.e., reproductive timing, growth rate, number and size of offspring). The endocrine system shapes phenotype by organizing tissues during developmental periods and by activating changes in behavior, physiology, and morphology in response to varying physical and social environments. Because hormones can simultaneously regulate many traits (hormonal pleiotropy), they are important mediators of life history trade-offs among growth, reproduction, and survival. This chapter reviews the role of hormones in shaping life histories with an emphasis on developmental plasticity and reversible flexibility in endocrine and life history traits. It also discusses the advantages of studying hormone–behavior interactions from an evolutionary perspective. Recent research in evolutionary endocrinology has provided insight into the heritability of endocrine traits, how selection on hormone systems may influence the evolution of life histories, and the role of hormonal pleiotropy in driving or constraining evolution.


2021 ◽  
Author(s):  
Anik Dutta ◽  
Fanny E. Hartmann ◽  
Carolina Sardinha Francisco ◽  
Bruce A. McDonald ◽  
Daniel Croll

AbstractThe adaptive potential of pathogens in novel or heterogeneous environments underpins the risk of disease epidemics. Antagonistic pleiotropy or differential resource allocation among life-history traits can constrain pathogen adaptation. However, we lack understanding of how the genetic architecture of individual traits can generate trade-offs. Here, we report a large-scale study based on 145 global strains of the fungal wheat pathogen Zymoseptoria tritici from four continents. We measured 50 life-history traits, including virulence and reproduction on 12 different wheat hosts and growth responses to several abiotic stressors. To elucidate the genetic basis of adaptation, we used genome-wide association mapping coupled with genetic correlation analyses. We show that most traits are governed by polygenic architectures and are highly heritable suggesting that adaptation proceeds mainly through allele frequency shifts at many loci. We identified negative genetic correlations among traits related to host colonization and survival in stressful environments. Such genetic constraints indicate that pleiotropic effects could limit the pathogen’s ability to cause host damage. In contrast, adaptation to abiotic stress factors was likely facilitated by synergistic pleiotropy. Our study illustrates how comprehensive mapping of life-history trait architectures across diverse environments allows to predict evolutionary trajectories of pathogens confronted with environmental perturbations.


2014 ◽  
Vol 161 (11) ◽  
pp. 2609-2619 ◽  
Author(s):  
Jefferson Murua ◽  
Michael T. Burrows ◽  
Roger N. Hughes ◽  
Stephen J. Hawkins ◽  
Richard C. Thompson ◽  
...  

2007 ◽  
Vol 363 (1490) ◽  
pp. 375-398 ◽  
Author(s):  
John R Speakman

Life-history trade-offs between components of fitness arise because reproduction entails both gains and costs. Costs of reproduction can be divided into ecological and physiological costs. The latter have been rarely studied yet are probably a dominant component of the effect. A deeper understanding of life-history evolution will only come about once these physiological costs are better understood. Physiological costs may be direct or indirect. Direct costs include the energy and nutrient demands of the reproductive event, and the morphological changes that are necessary to facilitate achieving these demands. Indirect costs may be optional ‘compensatory costs’ whereby the animal chooses to reduce investment in some other aspect of its physiology to maximize the input of resource to reproduction. Such costs may be distinguished from consequential costs that are an inescapable consequence of the reproductive event. In small mammals, the direct costs of reproduction involve increased energy, protein and calcium demands during pregnancy, but most particularly during lactation. Organ remodelling is necessary to achieve the high demands of lactation and involves growth of the alimentary tract and associated organs such as the liver and pancreas. Compensatory indirect costs include reductions in thermogenesis, immune function and physical activity. Obligatory consequential costs include hyperthermia, bone loss, disruption of sleep patterns and oxidative stress. This is unlikely to be a complete list. Our knowledge of these physiological costs is currently at best described as rudimentary. For some, we do not even know whether they are compensatory or obligatory. For almost all of them, we have no idea of exact mechanisms or how these costs translate into fitness trade-offs.


2015 ◽  
Vol 8 (7) ◽  
pp. 635-649 ◽  
Author(s):  
Emilie Snell‐Rood ◽  
Rickey Cothran ◽  
Anne Espeset ◽  
Punidan Jeyasingh ◽  
Sarah Hobbie ◽  
...  

Ecology ◽  
2015 ◽  
Vol 96 (9) ◽  
pp. 2499-2509 ◽  
Author(s):  
Michael P. Moore ◽  
Tobias Landberg ◽  
Howard H. Whiteman

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