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Self-incompatibility (SI) is a general name for several genetic mechanisms that prevent self-fertilization in sexually reproducing organisms, and thus encourage outcrossing and allogamy. It is contrasted with separation of sexes among individuals , and their various modes of spatial and temporal separation.
Self-pollination is a form of pollination in which pollen arrives at the stigma of a flower (in flowering plants) or at the ovule (in gymnosperms) of the same plant. The term cross-pollination is used for the opposite case, where pollen from one plant moves to a different plant.
Plant species where normal mode of seed set is through a high degree of cross-pollination have characteristic reproductive features and population structure. Existence of self-sterility, [1] self-incompatibility, imperfect flowers, and mechanical obstructions make the plant dependent upon foreign pollen for normal seed set. Each plant receives ...
Reproductive assurance (fertility assurance) occurs as plants have mechanisms to assure full seed set through selfing when outcross pollen is limiting. It is assumed that self-pollination is beneficial, in spite of potential fitness costs, when there is insufficient pollinator services or outcross pollen from other individuals to accomplish full seed set..
Several hypotheses have been proposed to explain the repeated independent evolution of heterostyly as opposed to homostylous self-incompatibility: 1) that heterostyly has evolved as a mechanism to reduce male gamete wastage on incompatible stigmas and to increase fitness through male function through reciprocal herkogamy; 2) heterostyly evolved ...
Self-pollination is an example of autogamy that occurs in flowering plants. Self-pollination occurs when the sperm in the pollen from the stamen of a plant goes to the carpels of that same plant and fertilizes the egg cell present. Self-pollination can either be done completely autogamously or geitonogamously. In the former, the egg and sperm ...
They evolved mechanisms to reduce self-pollination by changing the timing of maturity of the male and female parts. This altered timing mechanism or dichogamy was principally expressed by protogyny or the early maturation of the female parts and only rarely by protandry or the early maturation of the male parts. [10]
Allogamy ordinarily involves cross-fertilization between unrelated individuals leading to the masking of deleterious recessive alleles in progeny. [11] [12] By contrast, close inbreeding, including self-fertilization in plants and automictic parthenogenesis in hymenoptera, tends to lead to the harmful expression of deleterious recessive alleles (inbreeding depression).