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Related to self-pollination: cross-pollination


the transfer of pollen from the anthers to the stigma of the same flower or of another flower on the same plant



the transfer of pollen from the stamen of a flower to the stigma of the same flower (autogamy) or to the stigma of another flower of the same plant (geitonogamy). According to their capacity for self-pollination, plants are distinguished as those that are self-fertile and those that are self-sterile. Self-fertile plants, which include oats, peas, and barley, produce normal seeds through self-pollination. Self-pollination generally occurs in the flower bud, whereas “alien” pollen, which may play a subsequent role in fertilization, usually falls on the stigma of an already opened flower. Self-pollination occurs rarely in wild plants; it occurs in cultivated plants considerably more often. However, even in self-fertile plants, self-pollination apparently leads to gradual degeneration of varieties, and periodic intravarietal cross-pollination is conducted to increase viability.

Self-sterile plants that have been self-pollinated either do not produce seeds or produce underdeveloped seeds from which stunted plants develop. Self-sterility may be explained by self-incompatibility, that is, the inability of male and female sex cells descended from a single flower to merge and form an embryo. In cross-pollinators, self-incompatibility is controlled by special genes that inhibit growth of the pollen tubule on its own stigma or along the column of the pistil or, finally, inhibit the merging of sex cells and development of the embryo. Fundamental to these processes is the apparent capacity of the plants to elaborate substances similar to antibodies that inhibit the development of pollen on their own stigma. The manifestation of genes of incompatibility is strongly influenced by external conditions, which may partially or completely suppress their effects. The degree of self-incompatibility is usually not identical in different individuals of the same variety or species. Nor is it the same during the different periods of flowering, thereby making it possible to overcome self-incompatibility in selection work. I. V. Michurin used a number of artificial methods in his experiments.

In many plants, self-pollination occurs at the end of the flowering period, serving as a “reserve” phenomenon in the event that normal cross-pollination has not occurred. To ensure self-fertilization, plants have elaborated special adaptations—for example, changes in the position of the flower and the turning of the stigmas toward the stamens or of the stamens toward the stigmas.


Darwin, C. Deistvie perekrestnogo opyleniia i samoopyleniia ν rastitel’nom mire. Moscow-Leningrad, 1939.
Lobashov, M. E. Genetika, 2nd ed. Leningrad, 1967.
Pervukhina, N. V. Problemy morfologii i biologii tsvetka. Leningrad, 1970.
Kugler, H. Blütenökologie, 2nd ed. Jena, 1970.



[¦self ‚päl·ə¦nā·shən]
Transfer of pollen from the anther to the stigma of the same flower or of another flower on the same plant.
References in periodicals archive ?
The results also confirm the existence of self-pollination and the qualitative and quantitative production gain appears to be dependent on biotic pollination, in particular on the service provided by bees (Apis mellifera in this study), one of the most important pollinating species associated with many species of wild bees (KLEIN et al.
f] was calculated by dividing the mean number of seeds per fruit in the self-pollination treatment by the number of seeds in the artificial cross-pollination treatment.
The following tests were carried out to evaluate the breeding system: 1-Manual self-pollination (autogamy); 2-Cross-pollination (xenogamy).
2007; Aguiar and Gaglianone, 2008), self-pollination, since the species are normally cross-pollinated (Nogueira and Arruda, 2006) and abiotic factors such as temperature, humidity and precipitation (Ferreira et al.
Primack (1985) and Schoen and Ashman (1995) suggested that species capable of self-pollination have shorter longevity of flowers than outcrossing species.
Self-pollination did not produce a general loss in yield traits, therefore selfing-derived clones can be used to produce hybrid vigor in crossings.
The percentage of self-pollination (auto-fertility) at the studied sunflower hybrids in the period 2002-2008 registered a wide variation, ranging from 18% to 98%, but not at all been correlated with the nectar secretion, respectively the potential honey production (table 2 and figure 3).
Flowers that were isolated for verification of spontaneous self-pollination and agamospermy did not initiate fruit development, which indicates the dependence of B.
But although some flowers do self-fertilise, plants have evolved myriad physical strategies to avoid self-pollination and self-fertilisation.