Fluctuating selection

Alleles A and B fluctuate in adaptive value over time

Fluctuating selection is a mode of natural selection characterized by the fluctuation of the direction of selection on a given phenotype over a relatively brief period of evolutionary time. For example, a species of plant may come in two varieties: one which prefers wetter soil and one which prefers dryer soil. During a period of wet years, the wet variety will be more fit and produce more offspring, and thereby increase the frequency of wet-preferring plants. If this wet period is followed by drought, the dry variety will be selected for and its numbers will increase. As periods of dryness and wetness fluctuate, so too does selection on dry-preferring and wet-preferring plants. Fluctuating selection is also manifest at the genic level. Consider two alleles, A and B, which are found at the same locus. Fluctuating selection dynamics are at play when selection favors A at time t0, B at t1 and A again at t2.

Fluctuating selection has been characterized by several mathematical models. [1][2][3] Such models have led to the identification of fluctuating selection dynamics in evolving populations from a broad range of taxa, including bacteria, eukaryotes and viruses. [4][5][6]

Fluctuating selection, Red Queen dynamics and the maintenance of sex

The Red Queen hypothesis describes coevolutionary ‘arms races’ between antagonistic species (predators and prey, parasites and hosts, competitors with overlapping niches), emphasizing competition between species and populations rather than within them. Under Red Queen dynamics, a species must adapt to shifting selection pressures of the ever-changing biota which constitute its environment or face extinction. Experiments in Red Queen environments on real and simulated populations have offered strong support for the maintenance of sexual reproduction despite the two-fold cost of sex. [7][8]

Fluctuating selection may also play an important role in host-parasite coevolutionary relationships, specifically in the maintenance of sex. It has been shown that coevolutionary arms race dynamics between host and parasite give way to fluctuating selection dynamics in a minimal environment.[5] Fluctuating selection in Red Queen environments has been suggested as an explanation for the persistence of sex:

The essence of sex in our theory is that it stores genes that are currently bad but have promise for reuse. It continually tries them in combination, waiting for the time when the focus of disadvantage has moved elsewhere. When this has happened, the genotypes carrying such genes spread by successful reproduction, becoming simultaneously stores for other bad genes and thus onward in continuous succession.[7]

In this conception of sex, the population is a storehouse of variation and sex is a mechanism for distributing old, minority variants once they become useful. This theory depends on fluctuating selection, as fluctuating selection dynamics make adaptive previously maladaptive variants due to ecological shifts.

See also

References

  1. ↑ Haldane, J. B. S.; Jayakar, S. D. (1963). "Polymorphism due to selection of varying direction". Journal of Genetics 58 (2): 237–242. doi:10.1007/BF02986143. ISSN 0022-1333.
  2. ↑ Karlin, S.; Lieberman, Uri (1974). "Random temporal variation in selection intensities: Case of large population size". Theoretical Population Biology 6 (3): 355–382. doi:10.1016/0040-5809(74)90016-1. ISSN 0040-5809.
  3. ↑ Bell, G. (2010). "Fluctuating selection: the perpetual renewal of adaptation in variable environments". Philosophical Transactions of the Royal Society of London B: Biological Sciences 365 (1537): 87097. doi:10.1098/rstb.2009.0150. ISSN 0962-8436.
  4. ↑ Hairson, N. G.; Dillon, T. A. (1990). "Fluctuating Selection and Response in a Population of Freshwater Copepods". Evolution 44 (7): 1796–1805. doi:10.2307/2409508. ISSN 0014-3820. JSTOR 2409508.
  5. 1 2 Hall, A. R.; Scanlan, P. D.; Morgan, A. D.; Buckling, A. (2011). "Host-parasite coevolutionary arms races give way to fluctuating selection". Ecology Letters 14 (7): 635–642. doi:10.1111/j.1461-0248.2011.01624.x. ISSN 1461-023X.
  6. ↑ Sielpielski, A. M.; DiBattista, J. D.; Evans, J. A.; Carlson, S. M. (2011). "Differences in the temporal dynamics of phenotypic selection among fitness components in the wild". Proceedings of the Royal Society of London B: Biological Sciences 278 (1711): 1572–1580. doi:10.1098/rspb.2010.1973. ISSN 0962-8452.
  7. 1 2 Hamilton, W. D.; Axelrod, R.; Tanese, R. (1990). "Sexual reproduction as an adaptation to resist parasites (a review)". Proceedings of the National Academy of Sciences 87 (9): 3566–3573. doi:10.1073/pnas.87.9.3566. ISSN 0027-8424. PMID 2185476.
  8. ↑ Morran, L. T.; Schmidt, O. G.; Gelarden, I. A.; Parrish, R. C.; Lively, C. M. (2011). "Running with the Red Queen: Host-Parasite Coevolution Selects for Biparental Sex". Science 333 (6039): 216–218. doi:10.1126/science.1206360. ISSN 0036-8075. PMC 3402160. PMID 21737739.
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