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Visualizing Visual Adaptation
Published on: April 24, 2017
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Continuously fluctuating selection reveals fine granularity of adaptation
M C Bitter1, S Berardi2, H Oken2
1Department of Biology, Stanford University, Stanford, CA, USA. mcbitter@stanford.edu.
Nature
|August 14, 2024
Summary
Natural populations rapidly adapt to changing environments by shifting their genetic variation. This study shows that selection targets are predictable across years, even with fluctuating pressures.
Area of Science:
- Evolutionary Biology
- Population Genetics
- Ecology
Background:
- Natural habitats frequently present temporally fluctuating environmental conditions.
- Understanding how populations adapt to these dynamic conditions using standing genetic variation is crucial but remains largely unknown.
Purpose of the Study:
- To investigate the adaptive tracking of fluctuating selection pressures by natural populations.
- To analyze shifts in standing genetic variation over multiple generations in response to environmental changes.
Main Methods:
- Generated genome-wide allele frequency data every 1-2 generations for a diverse Drosophila melanogaster population over approximately 12 generations.
- Utilized replicated field mesocosms to simulate natural habitat conditions from late June to mid-December.
- Compared allele frequency changes with an independent dataset from the same experimental system.
Main Results:
- Observed extremely rapid and parallel changes in genomic variation across replicates, underpinning adaptation during population expansion, peak density, and collapse.
- Documented repeated fluctuations in the dominant direction of selection, even within ecological phases.
- Demonstrated that targets of selection are predictable across years.
Conclusions:
- Standing genetic variation has fitness relevance that may be obscured by static sampling or low-resolution time-series data.
- Fine-scaled, temporally fluctuating selection likely maintains functional genetic variation in natural populations.
- Fluctuating selection acts as a stochastic force impacting genome-wide diversity at linked neutral sites, similar to genetic draft.
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