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In population genetics, directional selection is a type of natural selection in which one extreme phenotype is favored over both the other extreme and moderate phenotypes. This genetic selection causes the allele frequency to shift toward the chosen extreme over time as allele ratios change from generation to generation.
The McDonald–Kreitman test [1] is a statistical test often used by evolutionary and population biologists to detect and measure the amount of adaptive evolution within a species by determining whether adaptive evolution has occurred, and the proportion of substitutions that resulted from positive selection (also known as directional selection).
The existence of limits in artificial selection experiments was discussed in the scientific literature in the 1940s or earlier. [1] The most obvious possible cause of reaching a limit (or plateau) when a population is under continued directional selection is that all of the additive-genetic variation (see additive genetic effects) related to that trait gets "used up" or fixed. [2]
Stabilizing selection (not to be confused with negative or purifying selection [1] [2]) is a type of natural selection in which the population mean stabilizes on a particular non-extreme trait value. This is thought to be the most common mechanism of action for natural selection because most traits do not appear to change drastically over time ...
Balancing selection refers to a number of selective processes by which multiple alleles (different versions of a gene) are actively maintained in the gene pool of a population at frequencies larger than expected from genetic drift alone. Balancing selection is rare compared to purifying selection. [1]
The first and most common function to estimate fitness of a trait is linear ω =α +βz, which represents directional selection. [1] [10] The slope of the linear regression line (β) is the selection gradient, ω is the fitness of a trait value z, and α is the y-intercept of the fitness function.
The Price equation can describe any system that changes over time, but is most often applied in evolutionary biology. The evolution of sight provides an example of simple directional selection. The evolution of sickle cell anemia shows how a heterozygote advantage can affect trait evolution. The Price equation can also be applied to population ...
This can result in stabilising selection through the purging of deleterious genetic polymorphisms that arise through random mutations. [2] [3] Purging of deleterious alleles can be achieved on the population genetics level, with as little as a single point mutation being the unit of selection. In such a case, carriers of the harmful point ...