Human Longevity at the Cost of Reproductive Success: Trade-Offs in the Life History

Author(s):  
T. B. L. Kirkwood ◽  
R. G. J. Westendorp
2012 ◽  
Vol 90 (9) ◽  
pp. 1072-1085 ◽  
Author(s):  
Marco Festa-Bianchet

Life-history trade-offs are well known in female mammals, but have seldom been quantified for males in polygynous species. I compared age-specific mass, weapon size, survival, and reproductive success of males in eight species of ungulates, and found weak interspecific correlations among life-history traits. Young males tended to have higher reproductive success in rapidly-growing than in slow-growing species, and in species where horns or antlers reached near-asymptotic size over the first few years of life. There was no clear interspecific trade-off between early reproduction and early survival. Reproductive senescence was evident in most species. Generation length, calculated as the mean age of fathers, was negatively correlated with the reproductive success of young males and positively with life expectancy of 3-year-olds, but not with early mortality. The main determinant of male reproductive success in polygynous ungulates is the ability to prevail against competing males. Consequently, the number and age structure of competitors should strongly affect an individual’s ability to reproduce, making classic trade-offs among life-history traits very context-dependent. Most fitness costs of reproduction in male ungulates likely arise from energy expenditure and injuries sustained while attempting to mate. Individual costs may be weakly correlated with fitness returns.


2006 ◽  
Vol 27 (3) ◽  
pp. 365-375 ◽  
Author(s):  
Delfi Sanuy ◽  
Christoph Leskovar ◽  
Neus Oromi ◽  
Ulrich Sinsch

AbstractDemographic life history traits were investigated in three Bufo calamita populations in Germany (Rhineland-Palatinate: Urmitz, 50°N; 1998-2000) and Spain (Catalonia: Balaguer, Mas de Melons, 41°N; 2004). We used skeletochronology to estimate the age as number of lines of arrested growth in breeding adults collected during the spring breeding period (all localities) and during the summer breeding period (only Urmitz). A data set including the variables sex, age and size of 185 males and of 87 females was analyzed with respect to seven life history traits (age and size at maturity of the youngest first breeders, age variation in first breeders, longevity, potential reproductive lifespan, median lifespan, age-size relationship). Spring and summer cohorts at the German locality differed with respect to longevity and potential reproductive lifespan by one year in favour of the early breeders. The potential consequences on fitness and stability of cohorts are discussed. Latitudinal variation of life history traits was mainly limited to female natterjacks in which along a south-north gradient longevity and potential reproductive lifespan increased while size decreased. These results and a review of published information on natterjack demography suggest that lifetime number of offspring seem to be optimized by locally different trade-offs: large female size at the cost of longevity in southern populations and increased longevity at the cost of size in northern ones.


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.


2021 ◽  
pp. 59-74
Author(s):  
Jeffrey A. Hutchings

Predictions about life-history evolution are intellectually bereft without a consideration of trade-offs. Benefits derived from making one life-history ‘decision’ are made at a cost of not realizing potential benefits associated with alternative decisions. These trade-offs are the inevitable product of constraints, often driven by an individual’s differential allocation of fixed resources to reproduction versus survival or growth. These allocations prevent multiple positive outcomes from being simultaneously realized. Reproductive effort is the proportion of total energy or resources allocated to all elements of reproduction. Reproductive effort generates reproductive costs. Increases in current reproductive effort reduce future reproductive success by affecting survival, growth, and/or fecundity. The causal mechanisms of these costs can be energetic, ecological, behavioural, or genetic. Evidence for reproductive costs is widespread. Instances where the evidence of costs is equivocal are usually caused by using among-individual correlations to study what is a within-individual phenomenon.


2018 ◽  
Vol 115 (17) ◽  
pp. 4441-4446 ◽  
Author(s):  
Mark R. Christie ◽  
Gordon G. McNickle ◽  
Rod A. French ◽  
Michael S. Blouin

The maintenance of diverse life history strategies within and among species remains a fundamental question in ecology and evolutionary biology. By using a near-complete 16-year pedigree of 12,579 winter-run steelhead (Oncorhynchus mykiss) from the Hood River, Oregon, we examined the continued maintenance of two life history traits: the number of lifetime spawning events (semelparous vs. iteroparous) and age at first spawning (2–5 years). We found that repeat-spawning fish had more than 2.5 times the lifetime reproductive success of single-spawning fish. However, first-time repeat-spawning fish had significantly lower reproductive success than single-spawning fish of the same age, suggesting that repeat-spawning fish forego early reproduction to devote additional energy to continued survival. For single-spawning fish, we also found evidence for a fitness trade-off for age at spawning: older, larger males had higher reproductive success than younger, smaller males. For females, in contrast, we found that 3-year-old fish had the highest mean lifetime reproductive success despite the observation that 4- and 5-year-old fish were both longer and heavier. This phenomenon was explained by negative frequency-dependent selection: as 4- and 5-year-old fish decreased in frequency on the spawning grounds, their lifetime reproductive success became greater than that of the 3-year-old fish. Using a combination of mathematical and individual-based models parameterized with our empirical estimates, we demonstrate that both fitness trade-offs and negative frequency-dependent selection observed in the empirical data can theoretically maintain the diverse life history strategies found in this population.


Nature ◽  
10.1038/25519 ◽  
1998 ◽  
Vol 396 (6713) ◽  
pp. 743-746 ◽  
Author(s):  
Rudi G. J. Westendorp ◽  
Thomas B. L. Kirkwood

2016 ◽  
Vol 3 (10) ◽  
pp. 160202 ◽  
Author(s):  
Pablo Brosset ◽  
Josep Lloret ◽  
Marta Muñoz ◽  
Christian Fauvel ◽  
Elisabeth Van Beveren ◽  
...  

Limited resources in the environment prevent individuals from simultaneously maximizing all life-history traits, resulting in trade-offs. In particular, the cost of reproduction is well known to negatively affect energy investment in growth and maintenance. Here, we investigated these trade-offs during contrasting periods of high versus low fish size and body condition (before/after 2008) in the Gulf of Lions. Female reproductive allocation and performance in anchovy ( Engraulis encrasicolus ) and sardine ( Sardina pilchardus ) were examined based on morphometric historical data from the 1970s and from 2003 to 2015. Additionally, potential maternal effects on egg quantity and quality were examined in 2014/2015. After 2008, the gonadosomatic index increased for sardine and remained steady for anchovy, while a strong decline in mean length at first maturity indicated earlier maturation for both species. Regarding maternal effects, for both species egg quantity was positively linked to fish size but not to fish lipid reserves, while the egg quality was positively related to lipid reserves. Atresia prevalence and intensity were rather low regardless of fish condition and size. Finally, estimations of total annual numbers of eggs spawned indicated a sharp decrease for sardine since 2008 but a slight increase for anchovy during the last 5 years. This study revealed a biased allocation towards reproduction in small pelagic fish when confronted with a really low body condition. This highlights that fish can maintain high reproductive investment potentially at the cost of other traits which might explain the present disappearance of old and large individuals in the Gulf of Lions.


2008 ◽  
Vol 4 (2) ◽  
pp. 200-203 ◽  
Author(s):  
Alexandra L Basolo

Understanding life-history evolution requires knowledge about genetic interactions, physiological mechanisms and the nature of selection. For platyfish, Xiphophorus maculatus , extensive information is available about genetic and physiological mechanisms influencing life-history traits. In particular, alleles at the pituitary locus have large and antagonistic effects on age and size at sexual maturation. To examine how predation affects the evolution of these antagonistic traits, I examined pituitary allele evolution in experimental populations differing in predation risk. A smaller size, earlier maturation allele increased in frequency when predators were absent, while a larger size, later maturation allele increased in frequency when predators were present. Thus, predation favours alleles for larger size, at the cost of later maturation and reproduction. These findings are interesting for several reasons. First, predation is often predicted to favour early reproduction at smaller sizes. Second, few studies have shown how selection acts on alleles that affect age and size at sexual maturation. Finally, many studies assume that trade-offs between these life-history traits result from antagonistic pleiotropy, with alleles that positively affect one trait negatively affecting another, yet this is rarely known. This study unequivocally demonstrates that genetically based trade-offs affect life-history evolution in platyfish.


2000 ◽  
Vol 13 (3) ◽  
pp. 409-414 ◽  
Author(s):  
Thomas ◽  
Teriokhin ◽  
Renaud ◽  
De Meeus ◽  
Guegan

2019 ◽  
Author(s):  
Eve Cooper ◽  
Timothée Bonnet ◽  
Helen Osmond ◽  
Andrew Cockburn ◽  
Loeske E. B. Kruuk

Why do senescence rates of fitness-related traits often vary dramatically? By considering the full ageing trajectories of multiple traits we can better understand how trade-offs and life-history shapes the unique evolution of senescence rates within a population. Here, we examine age-related changes in survival and six reproductive traits in both sexes using a long-term study of a wild population of a cooperatively-breeding songbird, the superb fairy-wren (Malurus cyaneus). We compare ageing patterns between traits by estimating standardized rates of maturation, the age of onset of senescence and rates of senescence, while controlling for confounding factors reflecting individual variability in life-history. We found striking differences in ageing and senescence patterns between survival and reproduction, and between the sexes. In both sexes, rates of survival started to decline from maturity onwards. In contrast, all reproductive traits showed improvements into early adulthood and many showed little or no evidence of senescence. Male reproductive ageing appeared to be driven by sexual selection, with extra-group reproductive success and sexually-selected plumage phenology showing much greater change with age than did within-group reproductive success. We discuss how the superb fairy-wrens’ complex life history may contribute to the disparate ageing patterns in this species.


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