scholarly journals The Geometry of Nutrient Space–Based Life-History Trade-Offs: Sex-Specific Effects of Macronutrient Intake on the Trade-Off between Encapsulation Ability and Reproductive Effort in Decorated Crickets

2018 ◽  
Vol 191 (4) ◽  
pp. 452-474 ◽  
Author(s):  
James Rapkin ◽  
Kim Jensen ◽  
C. Ruth Archer ◽  
Clarissa M. House ◽  
Scott K. Sakaluk ◽  
...  
Keyword(s):  
Life History ◽  
Reproductive Effort ◽  
Macronutrient Intake ◽  
Trade Off ◽  
Specific Effects ◽  
Trade Offs ◽  
Encapsulation Ability

The trade-off of reproduction and survival in slow-breeding seabirds

2010 ◽  
Vol 88 (9) ◽  
pp. 889-899 ◽  
Author(s):  
F. Stephen Dobson ◽  
Pierre Jouventin
Keyword(s):  
Life History ◽  
Body Size ◽  
Life History Traits ◽  
Feeding Rate ◽  
Reproductive Effort ◽  
Original Data ◽  
Age At Maturity ◽  
Trade Off ◽  
Trade Offs ◽  
Regression Techniques

A trade-off between reproduction and survival is one of the most consistent empirical aspects of life-history diversification. One explanation for this interspecific pattern is evolved differences in the balance of allocation to reproduction versus individual maintenance and survival. The same pattern is expected, however, simply as a result of differences among species in body size. We tested these alternatives using original data from 44 species of albatrosses and petrels, long-lived seabirds that breed very slowly. After application of regression techniques to remove the effects of body size and phylogeny, annual reproduction and survival exhibited a significant trade-off. Our measures of reproductive effort also exhibited significant trade-offs with age at maturity, the latter strongly associated with survival. Feeding rate of chicks, success at fledging chicks, and annual chick production were also significantly associated. In conclusion, after removing the effects of body size, we found a significant trade-off of reproduction and survival, in spite of the fact that these long-lived birds lay only one egg at a time. Our examination of the pattern among life-history traits of these slow breeders and their pelagic feeding ecology provide support for the evolutionary explanation of a trade-off of reproduction and survival.

scholarly journals Enzymatic antioxidants but not baseline glucocorticoids mediate the reproduction–survival trade-off in a wild bird

2018 ◽  
Vol 285 (1892) ◽  
pp. 20182141 ◽  
Author(s):  
Stefania Casagrande ◽  
Michaela Hau
Keyword(s):  
Life History ◽  
Body Condition ◽  
Redox State ◽  
Reproductive Investment ◽  
Redox System ◽  
Reactive Oxygen Metabolites ◽  
Enzymatic Antioxidants ◽  
Trade Off ◽  
Trade Offs ◽  
Nest Provisioning

The trade-off between reproductive investment and survival is central to life-history theory, but the relative importance and the complex interactions among the physiological mechanisms mediating it are still debated. Here we experimentally tested whether baseline glucocorticoid hormones, the redox system or their interaction mediate reproductive investment–survival trade-offs in wild great tits ( Parus major ). We increased the workload of parental males by clipping three feathers on each wing, and 5 days later determined effects on baseline corticosterone concentrations (Cort), redox state (reactive oxygen metabolites, protein carbonyls, glutathione peroxidase [GPx], total non-enzymatic antioxidants), body mass, body condition, reproductive success and survival. Feather-clipping did not affect fledgling numbers, chick body condition, nest provisioning rates or survival compared with controls. However, feather-clipped males lost mass and increased both Cort and GPx concentrations. Within feather-clipped individuals, GPx increases were positively associated with reproductive investment (i.e. male nest provisioning). Furthermore, within all individuals, males that increased GPx suffered reduced survival rates. Baseline Cort increases were related to mass loss but not to redox state, nest provisioning or male survival. Our findings provide experimental evidence that changes in the redox system are associated with the trade-off between reproductive investment and survival, while baseline Cort may support this trade-off indirectly through a link with body condition. These results also emphasize that plastic changes in individuals, rather than static levels of physiological signals, may mediate life-history trade-offs.

scholarly journals Warmer temperatures attenuate the classic offspring number and reproductive investment trade-off in the common lizard, Zootoca vivipara

2016 ◽  
Vol 12 (6) ◽  
pp. 20160101 ◽  
Author(s):  
Alexis Rutschmann ◽  
Donald B. Miles ◽  
Jean Clobert ◽  
Murielle Richard
Keyword(s):  
Life History ◽  
Environmental Conditions ◽  
Life History Traits ◽  
Natural Populations ◽  
Trade Off ◽  
Offspring Number ◽  
Common Lizard ◽  
Trade Offs ◽  
Zootoca Vivipara ◽  
The Common

Life-history traits involved in trade-offs are known to vary with environmental conditions. Here, we evaluate the response of the trade-off between ‘offspring number’ versus ‘energy invested per offspring’ to ambient temperature in 11 natural populations of the common lizard, Zootoca vivipara . We provide evidence at both the intra- and interpopulation levels that the trade-off is reduced with an increase in air temperature. If this effect enhances current individual fitness, it may lead to an accelerated pace of life in warmer environments and could ultimately increase adult mortality. In the context of global warming, our results advocate the need for more studies in natural populations to explore interactions between life-history traits' trade-offs and environmental conditions.

Life histories of North American game birds: a reanalysis

1988 ◽  
Vol 66 (8) ◽  
pp. 1906-1912 ◽  
Author(s):  
Todd W. Arnold
Keyword(s):  
Life History ◽  
North American ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Cost Of Reproduction ◽  
Reproductive Value ◽  
Trade Offs ◽  
Game Birds ◽  
The Cost

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.

Intraspecific variation in reproductive effort by female Parapediasia teterrella (Lepidoptera: Pyralidae) and its relation to body size

1990 ◽  
Vol 68 (1) ◽  
pp. 44-48 ◽  
Author(s):  
Larry D. Marshall
Keyword(s):  
Life History ◽  
Body Size ◽  
Egg Production ◽  
Egg Size ◽  
Reproductive Effort ◽  
Life History Evolution ◽  
Reproductive Parameters ◽  
Trade Offs ◽  
Egg Number ◽  
Lepidoptera Pyralidae

Daily egg production of the moth Parapediasia teterrella declined over the life-span of the female but egg size remained constant. The absence of water resulted in lower fecundity and early mortality. Egg size and lifetime fecundity showed considerable inter-individual variation and large females produced more and larger eggs than their smaller counterparts. Large females expended greater reproductive effort than small females. Hatching success was negatively related to egg size. In spite of this, large females laying large eggs had higher fitness than small females. I postulate that multiple reproductive strategies within a species, resulting from differences in reproductive effort expended, may explain why expected trade-offs in reproductive parameters (e.g., egg size versus egg number) were not found in this species. Furthermore, I argue that the prevalent interpretation of life-history evolution (that body size is the important determining parameter of life-history parameters) may reflect correlation of body size with reproductive effort, and reproductive effort may be more important in determining the nature of trade-offs between reproductive parameters.

scholarly journals Trade-off between age of first reproduction and survival in a female primate

2009 ◽  
Vol 5 (3) ◽  
pp. 339-342 ◽  
Author(s):  
Gregory E. Blomquist
Keyword(s):  
Life History ◽  
Life History Theory ◽  
Rhesus Macaques ◽  
Human Study ◽  
Genetic Correlations ◽  
Adult Survival ◽  
Trade Off ◽  
Trade Offs ◽  
Female Life History ◽  
First Reproduction

Trade-offs are central to life-history theory but difficult to document. Patterns of phenotypic and genetic correlations in rhesus macaques, Macaca mulatta —a long-lived, slow-reproducing primate—are used to test for a trade-off between female age of first reproduction and adult survival. A strong positive genetic correlation indicates that female macaques suffer reduced adult survival when they mature relatively early and implies primate senescence can be explained, in part, by antagonistic pleiotropy. Contrasts with a similar human study implicate the extension of parental effects to later ages as a potential mechanism for circumventing female life-history trade-offs in human evolution.

scholarly journals Using life history trade-offs to understand core-transient structuring of a small mammal community

2014 ◽  
Author(s):  
Sarah R Supp ◽  
David N. Koons ◽  
S. K. Morgan Ernest
Keyword(s):  
Life History ◽  
Reproductive Effort ◽  
Survival Strategies ◽  
Life History Strategies ◽  
High Survival ◽  
Transient Species ◽  
Ecological Specialization ◽  
Core Species ◽  
Trade Offs ◽  
Source Sink

An emerging conceptual framework suggests that communities are comprised of two main groups of species: core species that are temporally persistent, and transient species that are temporally intermittent. Core and transient species have been shown to differ in spatiotemporal turnover, diversity patterns, and importantly, survival strategies targeted at local vs. regional habitat use. While the core-transient framework has typically been a site-specific designation for species, we suggest that if core and transient species have local vs. regional survival strategies across sites, and consistently differ in population-level spatial structure and gene flow, they may also exhibit different life-history strategies. Specifically, core species should display relatively low dispersal rates, low reproductive effort, high ecological specialization and high survival rates compared to transient species, which may display a wider range of traits given that transience may result from source-sink dynamics or from the ability to emigrate readily. We present results from 21 years of capture-mark-recapture data in a diverse rodent community, evaluating the linkages between temporal persistence, local abundance, and trade-offs among life-history traits. Core species at our site conservatively supported our hypotheses, differing in ecological specialization, survival and dispersal probabilities, and reproductive effort from transient species. Transient species exhibited a wider range of characteristics, which likely stems from the multiple processes generating source-sink dynamics and nomadic transience in local communities. We suggest that trait associations among core-transient species may be similar in other systems and warrants further study.

scholarly journals Sex-specific patterns of senescence in artificial insect populations varying in sex-ratio to manipulate reproductive effort

2019 ◽  
Author(s):  
Charly Jehan ◽  
Manon Chogne ◽  
Thierry Rigaud ◽  
Yannick Moret
Keyword(s):  
Sex Ratio ◽  
Reproductive Effort ◽  
Male Reproduction ◽  
Sexually Dimorphic ◽  
Single Experiment ◽  
Sexual Competition ◽  
Trade Off ◽  
Trade Offs ◽  
Mealworm Beetle ◽  
Ratio Condition

Abstract Background The disposable soma theory of ageing assumes that organisms optimally trade-off limited resources between reproduction and longevity to maximize fitness. Early reproduction should especially trade-off against late reproduction and longevity because of reduced investment into somatic protection, including immunity. Moreover, as optimal reproductive strategies of males and females differ, sexually dimorphic patterns of senescence may evolve. In particular, as males gain fitness through mating success, sexual competition should be a major factor accelerating male senescence. In a single experiment, we examined these possibilities by establishing artificial populations of the mealworm beetle, Tenebrio molitor , in which we manipulated the sex-ratio to generate variable levels of investment into reproductive effort and sexual competition in males and females.Results As predicted, variation in sex-ratio affected male and female reproductive efforts, with contrasted sex-specific trade-offs between lifetime reproduction, survival and immunity. High effort of reproduction accelerated mortality in females, without affecting immunity, but high early reproductive success was observed only in balanced sex-ratio condition. Male reproduction was costly on longevity and immunity, mainly because of their investment into copulations rather than in sexual competition.Conclusions Our results suggest that T. molitor males, like females, maximize fitness through enhanced longevity, partly explaining their comparable longevity.

Reproductive Effort and Costs

2021 ◽  
pp. 59-74
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Reproductive Success ◽  
Total Energy ◽  
Reproductive Effort ◽  
Life History Evolution ◽  
Reproductive Costs ◽  
Positive Outcomes ◽  
Differential Allocation ◽  
Trade Offs ◽  
Potential Benefits

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.

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