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53 results for “life-history evolution”
Data from: Positive selection on sperm ion channels in a brooding brittle star: consequence of life-history traits evolution
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Data from: Temperature, size, reproductive allocation, and life-history evolution in a gregarious caterpillar
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Data from: Intraspecific divergence and evolution of a life-history trade-off along a successional gradient in Hawaii’s Metrosideros polymorpha
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Data from: Life-history and ecological variables as drivers of the evolution of avian innate immune defences
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Data from: Insulin-like growth factor 1 and life-history evolution of passerine birds
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Data from: Spatial selection and local adaptation jointly shape life-history evolution during range expansion
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Data from: Predation's role in life-history evolution of a livebearing fish and a test of the Trexler-DeAngelis model of maternal provisioning
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Data from: Human-mediated evolution in a threatened species? Juvenile life-history changes in Snake River salmon
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Data from: Joint reconstruction of divergence times and life-history evolution in placental mammals using a phylogenetic covariance model
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Data from: Sexual dimorphism explains residual variance around the survival-reproduction tradeoff in lizards: implications for sexual conflict over life-history evolution
The tradeoff between survival and reproduction is a central feature of life-history variation, but few studies have sought to explain why females of some species exhibit relatively lower survival than expected for a given level of reproductive effort. Intralocus sexual conflict theory proposes that sex differences in selection on survival and reproductive effort may, by virtue of shared genes underlying these components of fitness, prevent females from optimizing this life-history tradeoff. To test this hypothesis, we used a phylogenetically based comparative analysis of published estimates for mean annual survival and reproductive effort from females of 82 lizard species to (1) characterize the tradeoff between survival and reproduction, and (2) test whether variation around this tradeoff is explained by sexual size dimorphism (SSD), a potential proxy for sexual conflict over life-history traits. Across species, we found a strong negative correlation between mean annual survival and reproductive effort, confirming this classic life-history tradeoff. Although residual variance around this tradeoff is unrelated to the absolute magnitude of SSD, it is strongly related to the direction of SSD. Specifically, we found that females have lower survival than expected for a given level of reproductive effort in female-larger species, whereas they have higher survival than expected in male-larger species. Given that female-larger SSD is thought to reflect selection for increased fecundity, our results suggest that intralocus sexual conflict may be particularly likely to constrain female life-history evolution in situations where increased reproductive effort is favored, but the phenotypes that facilitate this increase (e.g., body size) are constrained by antagonistic selection on males.
Data from: Temporal genetic stability and high effective population size despite fisheries-induced life-history trait evolution in the North Sea sole.
Heavy fishing and other anthropogenic influences can have profound impact on a species' resilience to harvesting. Besides the decrease of the census and effective population size, strong declines in mature adults and recruiting individuals may lead to almost irreversible genetic changes in life-history traits. Here, we investigated the evolution of genetic diversity and effective population size in the heavily exploited sole (Solea solea), through the analysis of historical DNA from a collection of 1379 sole (Solea solea) otoliths dating back from 1957. Despite documented shifts in life-history traits, neutral genetic diversity inferred from 11 microsatellite markers showed a remarkable stability over a period of 50 years of heavy fishing. Using simulations and corrections for fisheries induced demographic variation, both point and temporal estimates of effective population size (Ne) were always higher than 1000, suggesting that despite the severe census size decrease over a 50 year period of harvesting, genetic drift is probably not strong enough to significantly decrease the neutral diversity of this species in the North Sea. However the ratio of effective population size to the census size (Ne/Nc) was very small (10-5), suggesting that overall only few adults contribute to the next generation. The high Ne level together with the low Ne/Nc ratio is most likely caused by a combination of an equalized reproductive output of younger cohorts, a decrease in generation time and a large variance in reproductive success typical for marine species. Because strong evolutionary changes in age and size at first maturation have been observed for sole, changes in adaptive genetic variation should be further monitored to detect the evolutionary consequences of human-induced selection.
Data from: Life-history evolution and density-dependent growth in experimental populations of yeast
We studied the evolution of the correlation between growth rate r and yield K in experimental lineages of the yeast Saccharomyces cerevisiae. First, we isolated a single clone every ~250 generations from each of eight populations selected in a glucose-limited medium for 5000 generations at ~6.6 population doublings per day (20 clones per line × 8 lines) and measured its growth rate and yield in a new, galactose-limited medium (with ~1.3 doubling per day). For most lines, r on galactose increased throughout the 5000 generations of selection on glucose while K on galactose declined. Next, we selected these 160 glucose-adapted clones in the galactose environment for ~120 generations and measured changes in r and K in galactose. In general, growth rate increased and yield declined, and clones that initially grew slowly on galactose improved more than did faster clones. We found a negative correlation between r and K among clones both within each line and across all clones. We provide evidence that this relationship is not heritable and is a negative environmental correlation rather than a genetic trade-off.
Data from: Towards a general perspective on life-history evolution and diversification in parasitoid wasps
In attempting to explain the marked interspecific variation evident in many components of life-history in parasitoid wasps, biologists have sought to identify general predictors of suites of 'important' life-history traits. Two predictors currently in general use are: (1) the parasitoid mode of larval development in relation to future host growth and development [no further host growth and development (= idiobiosis) versus continued host growth and development (= koinobiosis)]; and (2) the ovigeny index (the degree to which the lifetime potential complement of eggs is mature at the start of adult life in females). These have been postulated to share several life-history correlates, and an earlier comparative analysis showed the predictors to be associated. Two questions are thus posed: which life-history variables are actually common to both idio/koinobiosis and the ovigeny index, and which are responsible for the link between these two axes of life-history diversity? Through comparative analyses of a database of life-history traits for 133 parasitoid wasp species, four life-history correlates out of the 11 we investigated are shown to account for the association between the two predictors: the relative level of resource investment per egg (degree of yolk richness, which is lower in koinobionts), pre-adult lifespan (longer in koinobionts), female lifespan (shorter in koinobionts), and maximum egg load (larger in koinobionts). Our findings pave the way for full integration of the dichotomous hypothesis with the ovigeny index hypothesis, to provide a holistic perspective on parasitoid wasp life-history diversity and evolution.
Data from: Reasons for success: rapid evolution for desiccation resistance and life-history changes in the polyphagous fly Anastrepha ludens
Species that exhibit broad ranges of distribution may successfully navigate environmental changes by modifying some of their life history traits. Environmental humidity imposes a critical stress that organisms may overcome by increasing their resistance to desiccation. We used experimental evolution to investigate adaptation to desiccation in the tephritid Anastrepha ludens, a species with high fecundity, late maturation and long lifespan. We measured morphological, physiological, developmental as well as demographic changes involved in the adaptation to desiccation. Notwithstanding a low heritability (h2 = 0.237), desiccation resistance evolved extremely rapidly and few negative trade-offs were detected. Selected flies exhibited correlated increases in longevity, body size, the amount of body lipids and bulk water content, and in the duration of the pupal stage. Females further delayed sexual maturation, decreased daily fecundity but retained high lifetime reproductive potential. No differences in male mating competitiveness were found. Selected and control lines differed in longevity but not in total female fecundity, demonstrating that A. ludens flies have the capability for fast adaptation to desiccation without loosing their reproductive capability. Thus, it seems that a rapid evolutionary response to desiccation in this polyphagous insect works as a buffer for environmental variation and reduces the strength of selection on reproductive traits.
Data from: Life-history evolution in response to changes in metapopulation structure in an arthropod herbivore
The persistence and dynamics of populations largely depends on the way they are configured and integrated into space and the ensuing eco-evolutionary dynamics. We manipulated spatial and temporal variation in patch size in replicated experimental metapopulations of the herbivore mite Tetranychus urticae and followed evolutionary dynamics over approximately 30 generations. A significant divergence in life history traits, physiological endpoints and gene expression was recorded in the spatially and spatiotemporally variable metapopulation, but also a remarkable convergence relative to the stable reference metapopulation in traits related to size and fecundity and in its transcriptional regulation. The observed evolutionary dynamics are tightly linked to demographic changes, more specifically frequent episodes of resource shortage that increased the reproductive performance of mites on tomato, a challenging host plant. This points towards a general, adaptive stress response in stable spatial variable and spatiotemporal variable metapopulations that pre-adapts a herbivore arthropod to novel environmental stressors.
Data from: Bioinvasion triggers rapid evolution of life-histories in freshwater snails
Biological invasions offer interesting situations to observe how novel interactions between closely related, formerly allopatric species may trigger phenotypic evolution in situ. Assuming that successful invaders are usually filtered to be competitively dominant, invasive and native species may follow different trajectories. Natives may evolve traits that minimize the negative impact of competition, while trait shifts in invasives should mostly reflect expansion dynamics, through selection for colonization ability and transiently enhanced mutation load at the colonization front. These ideas were tested through a large-scale common-garden experiment measuring life-history traits in two closely related snail species, one invasive and one native, co-occurring in a network of freshwater ponds in Guadeloupe. We looked for evidence of recent evolution by comparing uninvaded or recently invaded with long-invaded sites. The native species adopted a life history favoring rapid population growth (i.e. increased fecundity, earlier reproduction and increased juvenile survival) that may increase its prospects of coexistence with the more competitive invader. We discuss why these effects are more likely to result from genetic change than from maternal effects. The invader exhibited slightly decreased overall performances in recently colonized sites, consistent with a moderate expansion load resulting from local founder effects. Our study highlights a rare example of rapid life-history evolution following invasion.
Figure 1 in Fly parasitism in Papuan frogs, with a discussion of ecological factors influencing evolution of life-history differences
Figure 1. Preserved specimen of Rana supragrisea showing enlarged swellings caused by three (two on right side, one on left) infesting larvae of Batrachomyia krausi. Apertures in the skin used to maintain larval access to air are clear on the right; larval respiratory spiracles project from the aperture on left.
Data from: Life-history evolution and density-dependent growth in experimental populations of yeast
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Data from: Temporal genetic stability and high effective population size despite fisheries-induced life-history trait evolution in the North Sea sole.
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Data from: Sex-dependent evolution of life-history traits following adaptation to climate warming
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Allen Brain Atlas
Allen Brain Atlas is an Allen Institute collection of brain map atlases, datasets, APIs, and analysis tools covering mouse, human, and non-human primate brain resources.
Annotated Behaviour and Observability Dataset (ABODe)
ABODe is a University of Edinburgh DataShare dataset for behavior classification in group-housed mice using home-cage video, identities, bounding boxes, ground-plate positions, and annotator labels.
DANDI Archive for NWB datasets
DANDI is a BRAIN Initiative archive for publishing and sharing neurophysiology data, including electrophysiology, optophysiology, and behavioral data packaged as NWB and related standards.
International Brain Laboratory public data
The International Brain Laboratory public data releases expose standardized mouse decision-making experiments, including Neuropixels recordings, widefield calcium imaging, behavior, and session metadata accessed through the ONE API.
OpenNeuro
OpenNeuro is a free, open platform for sharing neuroimaging datasets, with public search, dataset pages, and download paths for web, S3, DataLad, and the OpenNeuro CLI.