scholarly journals Beneficial cumulative effects of old parental age on offspring fitness

2021 ◽  
Vol 288 (1960) ◽  
Author(s):  
Laura M. Travers ◽  
Hanne Carlsson ◽  
Martin I. Lind ◽  
Alexei A. Maklakov
Keyword(s):  
Life Histories ◽  
Life History Traits ◽  
Detrimental Effect ◽  
Cumulative Effects ◽  
Parental Age ◽  
Negative Effects ◽  
Single Generation ◽  
Offspring Fitness ◽  
Young Parent ◽  
Successive Generations

Old parental age is commonly associated with negative effects on offspring life-history traits. Such parental senescence effects are predicted to have a cumulative detrimental effect over successive generations. However, old parents may benefit from producing higher quality offspring when these compete for seasonal resources. Thus, old parents may choose to increase investment in their offspring, thereby producing fewer but larger and more competitive progeny. We show that Caenorhabditis elegans hermaphrodites increase parental investment with advancing age, resulting in fitter offspring who reach their reproductive peak earlier. Remarkably, these effects increased over six successive generations of breeding from old parents and were subsequently reversed following a single generation of breeding from a young parent. Our findings support the hypothesis that offspring of old parents receive more resources and convert them into increasingly faster life histories. These results contradict the theory that old parents transfer a cumulative detrimental ‘ageing factor’ to their offspring.

scholarly journals Beneficial cumulative effects of old parental age on offspring fitness

2021 ◽  
Author(s):  
Laura. M. Travers ◽  
Hanne Carlsson ◽  
Martin I. Lind ◽  
Alexei A. Maklakov
Keyword(s):  
Life Histories ◽  
Life History Traits ◽  
Detrimental Effect ◽  
Parental Age ◽  
Negative Effects ◽  
High Quality ◽  
Parental Effect ◽  
Offspring Fitness ◽  
Young Parent ◽  
Successive Generations

AbstractOld parental age is commonly associated with negative effects on offspring life-history traits. Such parental effect senescence is predicted to have a cumulative detrimental effect over successive generations. However, old parents may benefit from producing high-quality offspring when these compete for seasonal resources. Thus, old parents may choose to increase investment in their offspring, thereby producing fewer but larger and more competitive progeny. We show that Caenorhabditis elegans hermaphrodites increase parental investment with advancing age, resulting in fitter offspring who reach their reproductive peak earlier. Remarkably, these effects increased over six successive generations of breeding from old parents and were subsequently reversed following a single generation of breeding from a young parent. These results contradict the theory that old parents transfer a cumulative detrimental “ageing factor” to their offspring. Instead, our findings support the hypothesis that offspring of old parents receive more resources and convert them into increasingly faster life-histories.

scholarly journals Echoes of the hunt? An inter-continental comparison of patterns of growth and determinants of size of brown bears in Canada and Sweden.

2022 ◽  
Author(s):  
Andreas Zedrosser ◽  
Marc CAttet ◽  
Jon Swenson ◽  
Gordon Stenhouse
Keyword(s):  
Population Density ◽  
Body Length ◽  
Life Histories ◽  
Life History Traits ◽  
Reproductive Investment ◽  
Negative Effects ◽  
Brown Bears ◽  
Positive Effects ◽  
The Past ◽  
The Difference

Comparing life history traits among populations that have been separated genetically for several hundred thousand years, but live in similar habitats on different continents, may help us understand how ecological and anthropomorphic factors shape life histories. We compared patterns of growth in body length and mass, and the influence of population density, habitat quality (NDVI), and reproduction on age-specific length and mass of male and female brown bears between Alberta, Canada, and Sweden. We found that Swedish females were significantly smaller in both length and mass than Alberta females. Swedish females also reached primiparity earlier and at a smaller mass and length. However, there were no continental differences in the patterns of growth in males. We found strong positive effects of NDVI, but only weak negative effects of population density on female mass and length in both areas. Generally, especially mass of Alberta females was more strongly affected by NDVI and density than for Swedish females. Reproduction had stronger negative effects on female mass in Alberta than in Sweden. We found no effects of NDVI and population density on male mass and body length in both areas. The larger variation in female growth and size between the areas, in contrast to males, may be related to differences in female reproductive investment due to differences in population trends, i.e., earlier reproduction in increasing populations or populations below carrying capacity, or to different selection pressures in the past, potentially due to human persecution. Swedish females exhibited characteristics typical of increasing populations, whereas Alberta females exhibited characteristics typical of stable or decreasing populations. The difference in reproduction investment means that Swedish bears can be harvested at higher rates, whereas Alberta bears must be managed more conservatively.

Hormones and Behavior

2019 ◽  
pp. 11-26
Author(s):  
Maren N. Vitousek ◽  
Laura A. Schoenle
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Traits ◽  
Developmental Plasticity ◽  
Endocrine System ◽  
Phenotypic Traits ◽  
Social Environments ◽  
Trade Offs ◽  
And Behavior

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.

A Primer of Life Histories

2021 ◽  
Author(s):  
Jeffrey A. Hutchings
Keyword(s):  
Life History ◽  
Life Histories ◽  
Life History Theory ◽  
Life History Traits ◽  
Reproductive Effort ◽  
Effective Means ◽  
Academic Experience ◽  
Sustainable Exploitation ◽  
Evolution Of Life ◽  
Opportune Time

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.

Temperature and parasite life-history are important modulators of the outcome of Trypanosoma rangeli–Rhodnius prolixus interactions

Parasitology ◽  
2016 ◽  
Vol 143 (11) ◽  
pp. 1459-1468 ◽  
Author(s):  
JULIANA DE O. RODRIGUES ◽  
MARCELO G. LORENZO ◽  
OLINDO A. MARTINS-FILHO ◽  
SIMON L. ELLIOT ◽  
ALESSANDRA A. GUARNERI
Keyword(s):  
Life Histories ◽  
Protozoan Parasite ◽  
Infection Rates ◽  
Trypanosoma Rangeli ◽  
Negative Effects ◽  
Temperature Dependent ◽  
Liver Infusion Tryptose ◽  
Insect Fitness ◽  
Different Levels

SUMMARYTrypanosoma rangeli is a protozoan parasite, which does not cause disease in humans, although it can produce different levels of pathogenicity to triatomines, their invertebrate hosts. We tested whether infection imposed a temperature-dependent cost on triatomine fitness using T. rangeli with different life histories. Parasites cultured only in liver infusion tryptose medium (cultured) and parasites exposed to cyclical passages through mice and triatomines (passaged) were used. We held infected insects at four temperatures between 21 and 30 °C and measured T. rangeli growth in vitro at the same temperatures in parallel. Overall, T. rangeli infection induced negative effects on insect fitness. In the case of cultured infection, parasite effects were temperature-dependent. Intermoult period, mortality rates and ecdysis success were affected in those insects exposed to lower temperatures (21 and 24 °C). For passaged-infected insects, the effects were independent of temperature, intermoult period being prolonged in all infected groups. Trypanosoma rangeli seem to be less tolerant to higher temperatures since cultured-infected insects showed a reduction in the infection rates and passaged-infected insects decreased the salivary gland infection rates in those insects submitted to 30 °C. In vitro growth of T. rangeli was consistent with these results.

scholarly journals Density Dependence, Evolutionary Optimization, and the Diversification of Avian Life Histories

The Condor ◽  
2000 ◽  
Vol 102 (1) ◽  
pp. 9-22 ◽  
Author(s):  
Robert E. Ricklefs
Keyword(s):  
Life History ◽  
Life Table ◽  
Life Histories ◽  
Life History Traits ◽  
Evolutionary Ecology ◽  
Reproductive Rate ◽  
Empirical Modeling ◽  
Adult Survival ◽  
Life History Variation ◽  
Evolutionary Response

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.

scholarly journals Temporal variation in temperature determines disease spread and maintenance in Paramecium microcosm populations

2011 ◽  
Vol 278 (1723) ◽  
pp. 3412-3420 ◽  
Author(s):  
Alison B. Duncan ◽  
Simon Fellous ◽  
Oliver Kaltz
Keyword(s):  
Temporal Variation ◽  
High Temperatures ◽  
Species Interactions ◽  
Life Histories ◽  
Variable Temperature ◽  
Parasite Prevalence ◽  
Disease Spread ◽  
Negative Effects ◽  
Environmental Variance ◽  
Variable Environment

The environment is rarely constant and organisms are exposed to temporal and spatial variations that impact their life histories and inter-species interactions. It is important to understand how such variations affect epidemiological dynamics in host–parasite systems. We explored effects of temporal variation in temperature on experimental microcosm populations of the ciliate Paramecium caudatum and its bacterial parasite Holospora undulata . Infected and uninfected populations of two P. caudatum genotypes were created and four constant temperature treatments (26°C, 28°C, 30°C and 32°C) compared with four variable treatments with the same mean temperatures. Variable temperature treatments were achieved by alternating populations between permissive (23°C) and restrictive (35°C) conditions daily over 30 days. Variable conditions and high temperatures caused greater declines in Paramecium populations, greater fluctuations in population size and higher incidence of extinction. The additional effect of parasite infection was additive and enhanced the negative effects of the variable environment and higher temperatures by up to 50 per cent. The variable environment and high temperatures also caused a decrease in parasite prevalence (up to 40%) and an increase in extinction (absence of detection) (up to 30%). The host genotypes responded similarly to the different environmental stresses and their effect on parasite traits were generally in the same direction. This work provides, to our knowledge, the first experimental demonstration that epidemiological dynamics are influenced by environmental variation. We also emphasize the need to consider environmental variance, as well as means, when trying to understand, or predict population dynamics or range.

scholarly journals Age-dependent effects of moderate differences in environmental predictability forecasted by climate change, experimental evidence from a short-lived lizard (Zootoca vivipara)

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
G. Masó ◽  
J. Kaufmann ◽  
H. Clavero ◽  
P. S. Fitze
Keyword(s):  
Climate Change ◽  
Life History ◽  
Environmental Conditions ◽  
Life History Traits ◽  
Negative Effects ◽  
Age Classes ◽  
Environmental Predictability ◽  
Common Lizard ◽  
Zootoca Vivipara ◽  
Age Dependent

Abstract Whether and how differences in environmental predictability affect life-history traits is controversial and may depend on mean environmental conditions. Solid evidence for effects of environmental predictability are lacking and thus, the consequences of the currently observed and forecasted climate-change induced reduction of precipitation predictability are largely unknown. Here we experimentally tested whether and how changes in the predictability of precipitation affect growth, reproduction, and survival of common lizard Zootoca vivipara. Precipitation predictability affected all three age classes. While adults were able to compensate the treatment effects, yearlings and juvenile females were not able to compensate negative effects of less predictable precipitation on growth and body condition, respectively. Differences among the age-classes’ response reflect differences (among age-classes) in the sensitivity to environmental predictability. Moreover, effects of environmental predictability depended on mean environmental conditions. This indicates that integrating differences in environmental sensitivity, and changes in averages and the predictability of climatic variables will be key to understand whether species are able to cope with the current climatic change.

scholarly journals Transgenerational effects of sexual interactions and sexual conflict: non-sires boost the fecundity of females in the following generation

2015 ◽  
Vol 11 (3) ◽  
pp. 20150067 ◽  
Author(s):  
Francisco Garcia-Gonzalez ◽  
Damian K. Dowling
Keyword(s):  
Sexual Selection ◽  
Life Histories ◽  
Direct Effects ◽  
Female Fitness ◽  
Transgenerational Effects ◽  
Female Fecundity ◽  
Sexual Interaction ◽  
Offspring Fitness ◽  
Generational Effects ◽  
Simple Production

The consequences of sexual interactions extend beyond the simple production of offspring. These interactions typically entail direct effects on female fitness, but may also impact the life histories of later generations. Evaluating the cross-generational effects of sexual interactions provides insights into the dynamics of sexual selection and conflict. Such studies can elucidate whether offspring fitness optima diverge across sexes upon heightened levels of sexual interaction among parents. Here, we found that, in Drosophila melanogaster , components of reproductive success in females, but not males, were contingent on the nature of sexual interactions experienced by their mothers. In particular, maternal sexual interactions with non-sires enhanced female fecundity in the following generation. This highlights the importance of non-sire influences of sexual interactions on the expression of offspring life histories.

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