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Inbreeding is also used to reveal deleterious recessive alleles, which can then be eliminated through assortative breeding or through culling. In plant breeding, inbred lines are used as stocks for the creation of hybrid lines to make use of the effects of heterosis. Inbreeding in plants also occurs naturally in the form of self-pollination.
In plants, selfing can occur as autogamous or geitonogamous pollinations and can have varying fitness affects that show up as autogamy depression. After several generations, inbreeding depression is likely to purge the deleterious alleles from the population because the individuals carrying them have mostly died or failed to reproduce.
Darwin's wife, Emma, was his first cousin, and he was concerned about the impact of inbreeding on his ten children, three of whom died at age ten or younger; three others had childless long-term marriages. [16] [17] [18] Humans do not seek to completely minimize inbreeding, but rather to maintain an optimal amount of inbreeding vs. outbreeding.
Therefore the coefficient of inbreeding of individual G is = (+) = + = %. If the parents of an individual are not inbred themselves, the coefficient of inbreeding of the individual is one-half the coefficient of relationship between the parents. This can be verified in the previous example, as 12.5% is one-half of 25%, the coefficient of ...
The effective population size (N e) is the size of an idealised population that would experience the same rate of genetic drift as the real population. [1] Idealised populations are those following simple one-locus models that comply with assumptions of the neutral theory of molecular evolution.
Sequential hermaphroditism can also protect against inbreeding in populations of organisms that have low enough motility and/or are sparsely distributed enough that there is a considerable risk of siblings encountering each other after reaching sexual maturity, and interbreeding.
The environment can directly affect the survival of a small population. Some detrimental effects include stochastic variation in the environment (year to year variation in rainfall, temperature), which can produce temporally correlated birth and death rates (i.e. 'good' years when birth rates are high and death rates are low and 'bad' years when birth rates are low and death rates are high ...
However, switches to selfing in annuals may result in an "evolutionary dead end," in the sense that it is probably unlikely to return to an outcrossing (allogamous) state. [13] Selfing and inbreeding can also result in the accumulation of deleterious alleles, resulting in inbreeding depression. [8]