Non-random mating occurs when certain genotypes are more likely to mate with each other, deviating from the assumptions of the Hardy-Weinberg equilibrium, which posits that all alleles in a population are mixed randomly. In non-random mating scenarios, the genotype frequencies are altered, pushing the population out of Hardy-Weinberg equilibrium, but importantly, the allele frequencies remain unchanged. This distinction is crucial because changes in allele frequencies are indicative of evolution.
It is essential to clarify that non-random mating is not synonymous with sexual selection. While non-random mating involves the pairing of alleles in a non-random manner, it assumes that all alleles still have the opportunity to be passed on. Sexual selection, on the other hand, focuses on the ability of organisms to obtain mates and successfully pass on their alleles.
One common form of non-random mating is inbreeding, which occurs when organisms mate with relatives, often due to geographical proximity. For instance, consider the distribution of white oak trees in the Eastern United States. Although these trees are wind-pollinated, pollen typically travels only about 200 meters. Therefore, an oak tree in Maine is unlikely to mate with one in Texas, as the wind cannot carry pollen that far. This localized mating leads to inbreeding, which increases homozygosity in the population, meaning there are more homozygotes than expected.
Increased homozygosity can result in inbreeding depression, characterized by a decrease in fitness due to the higher likelihood of pairing deleterious recessive alleles. Normally, these rare recessive alleles are masked by dominant alleles, but in inbred populations, the chance of these harmful alleles being expressed increases, leading to reduced fitness among individuals. While this decrease in fitness may suggest a potential for evolution, it is the subsequent natural selection that will drive changes in allele frequencies, ultimately leading to evolutionary changes in the population.
