scholarly journals Body Mass Increase Induced by Eight Years of Artificial Selection in the Yellow Mealworm (Coleoptera: Tenebrionidae) and Life History Trade-offs

2019 ◽  
Vol 19 (2) ◽  
Author(s):  
Juan A Morales-Ramos ◽  
Hans C Kelstrup ◽  
M Guadalupe Rojas ◽  
Virginia Emery
2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Bruno Simmen ◽  
Luca Morino ◽  
Stéphane Blanc ◽  
Cécile Garcia

AbstractLife history, brain size and energy expenditure scale with body mass in mammals but there is little conclusive evidence for a correlated evolution between life history and energy expenditure (either basal/resting or daily) independent of body mass. We addressed this question by examining the relationship between primate free-living daily energy expenditure (DEE) measured by doubly labeled water method (n = 18 species), life history variables (maximum lifespan, gestation and lactation duration, interbirth interval, litter mass, age at first reproduction), resting metabolic rate (RMR) and brain size. We also analyzed whether the hypometabolic primates of Madagascar (lemurs) make distinct energy allocation tradeoffs compared to other primates (monkeys and apes) with different life history traits and ecological constraints. None of the life-history traits correlated with DEE after controlling for body mass and phylogeny. In contrast, a regression model showed that DEE increased with increasing RMR and decreasing reproductive output (i.e., litter mass/interbirth interval) independent of body mass. Despite their low RMR and smaller brains, lemurs had an average DEE remarkably similar to that of haplorhines. The data suggest that lemurs have evolved energy strategies that maximize energy investment to survive in the unusually harsh and unpredictable environments of Madagascar at the expense of reproduction.


2020 ◽  
Author(s):  
Serena Wong ◽  
Jennifer S. Bigman ◽  
Nicholas K. Dulvy

AbstractAll life acquires energy through metabolic processes and that energy is subsequently allocated to life-sustaining functions such as survival, growth, and reproduction. Thus, it has long been assumed that metabolic rate is related to the life history of an organism. Indeed, metabolic rate is commonly believed to set the pace of life by determining where an organism is situated along a fast-slow life history continuum. However, empirical evidence of a relationship between metabolic rate and life histories is lacking, especially for ectothermic organisms. Here, we ask whether three life history traits – maximum body mass, generation length, and growth performance – explain variation in resting metabolic rate (RMR) across fishes. We found that growth performance, which accounts for the trade-off between growth rate and maximum body size, explained variation in RMR, yet maximum body mass and generation length did not. Our results suggest that measures of life history that encompass trade-offs between life history traits, rather than traits in isolation, explain variation in RMR across fishes. Ultimately, understanding the relationship between metabolic rate and life history is crucial to metabolic ecology and has the potential to improve prediction of the ecological risk of data-poor species.


2021 ◽  
Vol 288 (1953) ◽  
pp. 20210910
Author(s):  
Serena Wong ◽  
Jennifer S. Bigman ◽  
Nicholas K. Dulvy

All life acquires energy through metabolic processes and that energy is subsequently allocated to life-sustaining functions such as survival, growth and reproduction. Thus, it has long been assumed that metabolic rate is related to the life history of an organism. Indeed, metabolic rate is commonly believed to set the pace of life by determining where an organism is situated along a fast–slow life-history continuum. However, empirical evidence of a direct interspecific relationship between metabolic rate and life histories is lacking, especially for ectothermic organisms. Here, we ask whether three life-history traits—maximum body mass, generation length and growth performance—explain variation in resting metabolic rate (RMR) across fishes. We found that growth performance, which accounts for the trade-off between growth rate and maximum body size, explained variation in RMR, yet maximum body mass and generation length did not. Our results suggest that measures of life history that encompass trade-offs between life-history traits, rather than traits in isolation, explain variation in RMR across fishes. Ultimately, understanding the relationship between metabolic rate and life history is crucial to metabolic ecology and has the potential to improve prediction of the ecological risk of data-poor species.


2019 ◽  
Author(s):  
Cecina Babich Morrow ◽  
S. K. Morgan Ernest ◽  
Andrew J. Kerkhoff

AbstractLife history traits represent organism’s strategies to navigate the fitness trade-offs between survival and reproduction. Eric Charnov developed three dimensionless metrics to quantify fundamental life history trade-offs. Lifetime reproductive effort (LRE), relative reproductive lifespan (RRL), and relative offspring size (ROS), together with body mass, can be used classify life history strategies across the four major classes of tetrapods: amphibians, reptiles, mammals, and birds. First, we investigate how the metrics have evolved in concert with body mass. In most cases, we find evidence for correlated evolution between body mass and the three metrics. Finally, we compare life history strategies across the four classes of tetrapods and find that LRE, RRL, and ROS delineate a space in which the major tetrapod clades occupy mostly unique subspaces. These distinct combinations of life history strategies provide us with a framework to understand the impact of major evolutionary transitions in energetics, physiology, and ecology.


Author(s):  
Luis Giménez

Marine crustaceans show a suite of phenotypically plastic responses to the environment, with some restricted to the larval phase and others transcending life history boundaries, linking life phases or generations. Maternal effects include the effects of allocation of reserves into eggs as well as effects of the embryonic environment on tolerance to low salinity or larval body mass. Within the larval phase, there is a diversity of plastic responses involving changes in body size, growth, and developmental rate; they can occur within the molt cycle, involve several molting stages, or result in the development of alternative pathways characterized by the different larval stages. In feeding larvae, the effects of stressors on body mass may be attenuated by delayed development; however, in nonfeeding larvae (e.g., barnacle cyprids), delayed metamorphosis reduces juvenile body size and habitat selectivity. Also, larval food limitation and increased temperatures away from the optimum lead to reduced body mass during metamorphosis. Overall, many of these responses are adaptive and lead to the maintenance of basic functions at the expense of morphogenesis and growth. Some plastic responses that lead to changes in size during metamorphosis can also have consequences for juvenile size growth and survival. These “latent effects” appear to represent forms of developmental trade-offs and may have important ecological and evolutionary consequences. Larval plasticity, by generating phenotypic variation, may influence the capacity to compete, capture resources, tolerate stressors, and, ultimately, may affect recruitment dynamics. In addition, plastic responses linking life history stages also result in genetic links and hence drive the evolution of crustaceans with complex life cycles.


2017 ◽  
Vol 38 (1) ◽  
pp. 41-48
Author(s):  
Elena Buhaciuc ◽  
Paul Székely ◽  
Raluca Băncilă ◽  
Dan Cogălniceanu

Understanding how major life history traits such as body size and mass and growth change in response to resource availability is crucial in explaining life history trade-offs. We conducted a laboratory experiment with three (high, medium and low) feeding intensity treatments using metamorphs of two spadefoot toads species,Pelobates syriacusandP. fuscus, from syntopic populations. We tested how total food consumption, final body size and mass, body mass increase, body mass and length growth rates and growth efficiency are influenced by food availability. The responses to food availability differed significantly between the species with respect to the total food consumption, body mass increase, body mass growth rate and growth efficiency (i.e. the ratio between total amount of food consumed during the experiment divided by the increase in body mass).P. syriacusmetamorphs had higher growth rates and growth efficiency thanP. fuscusjuveniles. Also,P. syriacusjuveniles responded to differences in food level by increasing growth efficiency with decreasing food levels. OverallP. syriacusseems better adapted to shortages in food availability thanP. fuscus. Our results clearly indicate that the differences in body size between the two species originate between metamorphosis and sexual maturity.


2021 ◽  
Vol 288 (1949) ◽  
Author(s):  
Cecina Babich Morrow ◽  
S. K. Morgan Ernest ◽  
Andrew J. Kerkhoff

Life-history traits represent organisms' strategies to navigate the fitness trade-offs between survival and reproduction. Eric Charnov developed three dimensionless metrics to quantify fundamental life-history trade-offs. Lifetime reproductive effort (LRE), relative reproductive lifespan (RRL) and relative offspring size (ROS), together with body mass can be used to classify life-history strategies across the four major classes of tetrapods: amphibians, reptiles, mammals and birds. First, we investigate how the metrics have evolved in concert with body mass within tetrapod lineages. In most cases, we find evidence for correlated evolution among body mass and the three dimensionless metrics. Second, we compare life-history strategies across the four classes of tetrapods and find that LRE, RRL and ROS delineate a space in which the major tetrapod classes occupy mostly unique subspaces. These distinct combinations of life-history strategies provide us with a framework to understand the impact of major evolutionary transitions in energetics, physiology and ecology.


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.


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