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32 results for “Life history: aging”
Data from: Offspring provisioning explains clone specific maternal age effects on life history and lifespan in the water flea, Daphnia pulex
Genetic inheritance underpins evolutionary theories of aging, but the role that nongenetic inheritance plays is unclear. Parental age reduces the life span of offspring in a diverse array of taxa but has not been explained from an evolutionary perspective. We quantified the effect that maternal age had on the growth and maturation decisions, life history, rates of senescence, and life span of offspring from three Daphnia pulex clones collected from different populations. We then used those data to test general hypotheses proposed to explain maternal age effects on offspring life span. Three generations of breeding from young or old mothers produced dramatic differences in the life histories of fourth-generation offspring, including significant reductions in life span. The magnitude of the effect differed between clones, which suggests that genetic and nongenetic factors ultimately underpin trait inheritance and shape patterns of aging. Older parents did not transmit a senescent state to their offspring. Instead, offspring from older ancestors had increased early-life reproductive effort, which resulted in an earlier onset of reproductive senescence, and an increased rate of actuarial senescence, which shortened their life span. Our results provide a clear example of the need to consider multiple inheritance mechanisms when studying trait evolution.
Data from: Plastic responses of some life history traits and cellular components of body size in Aphidius ervi as related to the age of its host Acyrthosiphon pisum
Phenotypic plasticity of wing size and shape has been evaluated in Aphidius ervi developing in its host, Acyrthosiphon pisum, parasitized at seven different ages. The parasitoid wing size was used as an estimator of both whole body size and its cellular composition. No size difference was observed in A. ervi adults emerged from aphids 1, 2 or 3 days old at parasitization. Body size then increased in A. ervi emerged from hosts older at parasitization. Body size values as related to host age at parasitization were achieved by adjusting developmental time, developmental rate or both. Parasitoids of similar size, but developed in hosts parasitized at different ages, had different wing cellular composition, while the increase of parasitoid body size was related to a general increase in both cell area and cell number. These results seem to suggest a trade-off between adult size and developmental time, at least for parasitoids developed at the two extremes of host ages at parasitization, and that A. ervi can reach the same adult size via different trajectories, adapting its ontogenetic processes. Wing shape was typical for all the different parasitoid classes considered and differed strongly between males and females, independent of their size. Parasitoid males (haploids) and females (diploids) did not differ in either cell area or cell number, suggesting a possible sex-determined dosage compensation in somatic tissue endoreplication.
Testing size-frequency distributions as a method of ontogenetic aging: a life history assessment of hadrosaurid dinosaurs from the Dinosaur Park Formation of Alberta, Canada, with implications for hadrosaurid paleoecology
<p class="MsoNoSpacing">Hadrosaurid dinosaurs, the dominant large-bodied terrestrial herbivores in most Laurasian Late Cretaceous ecosystems, have an exceptional fossil record consisting of many species known from partial ontogenetic series making them an ideal clade with which to conduct life history studies. Previous research considered the Dinosaur Park Formation (DPF) of Alberta as an attritional, or time-averaged, sample and interpreted size-frequency distribution of long bones collected from the DPF with three size classes to suggest that hadrosaurids from the DPF attained near-asymptotic body size in under three years. This conflicted with previously published osteohistological estimates of 6+ years for penecontemporaneous hadrosaurids from the Two Medicine Formation (TMF) of Montana suggesting either extreme variation in hadrosaurid growth rates or that size-frequency distributions and/or osteohistology and growth modeling inaccurately estimate ontogenetic age.</p> <p>We tested the validity of the previously proposed size-age relationship of hadrosaurids from the DPF by significantly increasing sample size and combining data from size-frequency distributions and osteohistology across multiple long bones elements. The newly constructed size-frequency distributions typically reveal four relatively distinct size-frequency peaks that, when integrated with the osteohistological data, aligned with growth marks. The yearling size class was heavily underrepresented in the size-frequency distribution. If not due to preservation, this suggests that either juvenile (< 2 years of age) hadrosaurids from the DPF had increased survivorship following an initially high nestling mortality rate, or that yearlings were segregated from adults. A growth curve analysis revealed asymptotic body size was attained in approximately 7 years, which is consistent with hadrosaurids from the TMF. The data suggest size-frequency distributions of attritional samples underestimate age and overestimate growth rates, but when paired with osteohistology can provide unique life history insights.</p>
Data from: Maternal age at birth shapes offspring life-history trajectory across generations in long-lived Asian elephants
1. Advanced maternal age at birth can have pronounced consequences for offspring health, survival and reproduction. If carried over to the next generation, such fitness effects could have important implications for population dynamics and the evolution of ageing, but these remain poorly understood. While many laboratory studies have investigated maternal age effects, relatively few studies have been conducted in natural populations, and they usually only present a "snapshot" of an offspring's lifetime. 2. In the present study, we focus on how maternal age influences offspring life-history trajectories and performance in a long-lived mammal. 3. We use a multigenerational demographic dataset of semi-captive Asian elephants to investigate maternal age effects on several offspring life-history traits: condition, reproductive success, and overall survival. 4. We show that offspring born to older mothers display reduced overall survival but higher reproductive success, and reduced survival of their own progeny. Our results show evidence of a persistent effect of maternal age on fitness across generations in a long-lived mammal. 5. By highlighting transgenerational effects on the fitness of the next generation associated with maternal age, the present study helps increase our understanding of factors contributing to individual variation in ageing rates and fitness.
Data from: Ontogenetic timing as a condition-dependent life history trait: high-condition males develop quickly, peak early and age fast
Within-population variation in ageing remains poorly understood. In males, condition-dependent investment in secondary sexual traits may incur costs which limit ability to invest in somatic maintenance. Moreover, males often express morphological and behavioural secondary sexual traits simultaneously, but the relative effects on ageing of investment in these traits remain unclear. We investigated the condition-dependence of male life history in the neriid fly Telostylinus angusticollis. Using a fully factorial design, we manipulated male early-life condition by varying nutrient content of the larval diet and, subsequently, manipulated opportunity for adult males to interact with rival males. We found that high-condition males developed more quickly and reached their reproductive peak earlier in life, but also experienced faster reproductive ageing and died sooner than low-condition males. By contrast, interactions with rival males reduced male lifespan but did not affect male reproductive ageing. High condition in early life is therefore associated with rapid ageing in T. angusticollis males, even in the absence of damaging male-male interactions. Our results show that abundant resources during the juvenile phase are used to expedite growth and development and enhance early-life reproductive performance at the expense of late-life performance and survival, demonstrating a clear link between male condition and ageing.
Testing size-frequency distributions as a method of ontogenetic aging: a life history assessment of hadrosaurid dinosaurs from the Dinosaur Park Formation of Alberta, Canada, with implications for hadrosaurid paleoecology
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Data from: Ontogenetic timing as a condition-dependent life history trait: high-condition males develop quickly, peak early and age fast
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Data from: Offspring provisioning explains clone specific maternal age effects on life history and lifespan in the water flea, Daphnia pulex
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Data from: Plastic responses of some life history traits and cellular components of body size in Aphidius ervi as related to the age of its host Acyrthosiphon pisum
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Data from: Sex-specific mitonuclear epistasis and the evolution of mitochondrial bioenergetics, ageing and life history in seed beetles
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Data from: Maternal age at birth shapes offspring life-history trajectory across generations in long-lived Asian elephants
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Data from: Life history differences in age-dependent expressions of multiple ornaments and behaviors in a lekking bird
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