Temporal–spatial variation in white-tailed prairie dog demography and life histories in Wyoming

1989 ◽  
Vol 67 (2) ◽  
pp. 343-349 ◽  
Author(s):  
George E. Menkens Jr. ◽  
Stanley H. Anderson

Variation in population density and life history traits were studied in six white-tailed prairie dog (Cynomys leucurus) populations in Wyoming using mark – recapture techniques. All life history traits (except juvenile sex ratios) and population density exhibited significant variation within towns between years and among towns in the same year. Temporal and spatial habitat variation significantly affects juvenile body mass but not adult body mass, which, in turn, results in the observed variation in life history traits. We conclude that white-tailed prairie dogs are dynamic reproducers and that their population age distributions are neither stable nor stationary. Use of life tables to study life history patterns of this species or of similar species would be inappropriate because of a failure to meet a basic assumption of life table models.

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.


1986 ◽  
Vol 64 (12) ◽  
pp. 2739-2749 ◽  
Author(s):  
Richard M. Zammuto

Clutch size, longevity, and body mass data for 54 North American game birds were extracted from the literature to test the hypothesis that a trade-off exists between fecundity and survival among avian species. Species with larger clutch sizes live shorter lives than species with smaller clutch sizes (r = −0.38, n = 54, P < 0.01). This relationship still holds when the effects of body mass are removed (r = −0.34, 51 df, P < 0.05), indicating that the relationship is not simply a function of body mass. This latter finding is inconsistent with previous life-history studies, perhaps because previous researchers did not attempt to remove body mass effects from their life-history investigations. Results are similar (P < 0.05) when mean values of life-history traits are examined at the generic level. However, no relationships (P > 0.05) among mean values of life-history traits occur at any taxonomic level higher than genus or when species are grouped with respect to feeding habits. This might be the result of low sample size. I conclude that the evolution of clutch size is influenced by longevity, or vice versa, among species and genera of North American game birds.


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 ◽  
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.


Author(s):  
Jeffrey A. Hutchings

Life histories describe how genotypes schedule their reproductive effort throughout life in response to factors that affect their survival and fecundity. Life histories are solutions that selection has produced to solve the problem of how to persist in a given environment. These solutions differ tremendously within and among species. Some organisms mature within months of attaining life, others within decades; some produce few, large offspring as opposed to numerous, small offspring; some reproduce many times throughout their lives while others die after reproducing just once. The exponential pace of life-history research provides an opportune time to engage and re-engage new generations of students and researchers on the fundamentals and applications of life-history theory. Chapters 1 through 4 describe the fundamentals of life-history theory. Chapters 5 through 8 focus on the evolution of life-history traits. Chapters 9 and 10 summarize how life-history theory and prediction has been applied within the contexts of conservation and sustainable exploitation. This primer offers an effective means of rendering the topic accessible to readers from a broad range of academic experience and research expertise.


The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 9-22 ◽  
Author(s):  
Robert E. Ricklefs

Abstract Although we have learned much about avian life histories during the 50 years since the seminal publications of David Lack, Alexander Skutch, and Reginald Moreau, we still do not have adequate explanations for some of the basic patterns of variation in life-history traits among birds. In part, this reflects two consequences of the predominance of evolutionary ecology thinking during the past three decades. First, by blurring the distinction between life-history traits and life-table variables, we have tended to divorce life histories from their environmental context, which forms the link between the life history and the life table. Second, by emphasizing constrained evolutionary responses to selective factors, we have set aside alternative explanations for observed correlations among life-history traits and life-table variables. Density-dependent feedback and independent evolutionary response to correlated aspects of the environment also may link traits through different mechanisms. Additionally, in some cases we have failed to evaluate quantitatively ideas that are compelling qualitatively, ignored or explained away relevant empirical data, and neglected logical implications of certain compelling ideas. Comparative analysis of avian life histories shows that species are distributed along a dominant slow-fast axis. Furthermore, among birds, annual reproductive rate and adult mortality are directly proportional to each other, requiring that pre-reproductive survival is approximately constant. This further implies that age at maturity increases dramatically with increasing adult survival rate. The significance of these correlations is obscure, particularly because survival and reproductive rates at each age include the effects of many life-history traits. For example, reproductive rate is determined by clutch size, nesting success, season length, and nest-cycle length, each of which represents the outcome of many different interactions of an individual's life-history traits with its environment. Resolution of the most basic issues raised by patterns of life histories clearly will require innovative empirical, modeling, and experimental approaches. However, the most fundamental change required at this time is a broadening of the evolutionary ecology paradigm to include a variety of alternative mechanisms for generating patterns of life-history variation.


2017 ◽  
Vol 114 (5) ◽  
pp. 1069-1074 ◽  
Author(s):  
Helder Gomes Rodrigues ◽  
Anthony Herrel ◽  
Guillaume Billet

Investigating life history traits in mammals is crucial to understand their survival in changing environments. However, these parameters are hard to estimate in a macroevolutionary context. Here we show that the use of dental ontogenetic parameters can provide clues to better understand the adaptive nature of phenotypic traits in extinct species such as South American notoungulates. This recently extinct order of mammals evolved in a context of important geological, climatic, and environmental variations. Interestingly, notoungulates were mostly herbivorous and acquired high-crowned teeth very early in their evolutionary history. We focused on the variations in crown height, dental eruption pattern, and associated body mass of 69 notoungulate taxa, placed in their phylogenetic and geological contexts. We showed that notoungulates evolved higher crowns several times between 45 and 20 Ma, independently of the variation in body mass. Interestingly, the independent acquisitions of ever-growing teeth were systematically accompanied by eruption of molars faster than permanent premolars. These repeated associations of dental innovations have never been documented for other mammals and raise questions on their significance and causal relationships. We suggest that these correlated changes could originate from ontogenetic adjustments favored by structural constraints, and may indicate accelerated life histories. Complementarily, these more durable and efficient dentitions could be selected to cope with important ingestions of abrasive particles in the context of intensified volcanism and increasing aridity. This study demonstrates that assessing both life history and ecological traits allows a better knowledge of the specializations of extinct mammals that evolved under strong environmental constraints.


Biology ◽  
2020 ◽  
Vol 9 (12) ◽  
pp. 462
Author(s):  
Zuzanna M. Filipiak ◽  
Michał Filipiak

Bee nutrition studies have focused on food quantity rather than quality, and on details of bee biology rather than on the functioning of bees in ecosystems. Ecological stoichiometry has been proposed for studies on bee nutritional ecology as an ecosystem-oriented approach complementary to traditional approaches. It uses atomic ratios of chemical elements in foods and organisms as metrics to ask ecological questions. However, information is needed on the fitness effects of nutritional mismatches between bee demand and the supply of specific elements in food. We performed the first laboratory feeding experiment on the wild bee Osmia bicornis, investigating the impact of Na, K, and Zn scarcity in larval food on fitness-related life history traits (mortality, cocoon development, and imago body mass). We showed that bee fitness is shaped by chemical element availability in larval food; this effect may be sex-specific, where Na might influence female body mass, while Zn influences male mortality and body mass, and the trade-off between K allocation in cocoons and adults may influence cocoon and body development. These results elucidate the nutritional mechanisms underlying the nutritional ecology, behavioral ecology, and population functioning of bees within the context of nutrient cycling in the food web.


1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold

Recently, Zammuto (R. M. Zammuto. 1986. Can. J. Zool. 64: 2739–2749) suggested that North American game birds exhibited survival–fecundity trade-offs consistent with the "cost of reproduction" hypothesis. However, there were four serious problems with the data and the analyses that Zammuto used: (i) the species chosen for analysis ("game birds") showed little taxonomic or ecological uniformity, (ii) the measures of future reproductive value (maximum longevity) were severely biased by unequal sample sizes of band recoveries, (iii) the measures of current reproductive effort (clutch sizes) were inappropriate given that most of the birds analyzed produce self-feeding precocial offspring, and (iv) the statistical units used in the majority of analyses (species) were not statistically independent with respect to higher level taxonomy. After correcting these problems, I found little evidence of survival–fecundity trade-offs among precocial game birds, and I attribute most of the explainable variation in life-history traits of these birds to allometry, phylogeny, and geography.


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