Cleistogamy

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Chasmogamous (a) and cleistogamous (b) flowers of Viola pubescens. Arrows point to structure. Chasmogamy.jpg
Chasmogamous (a) and cleistogamous (b) flowers of Viola pubescens. Arrows point to structure.

Cleistogamy is a type of automatic self-pollination of certain plants that can propagate by using non-opening, self-pollinating flowers. Especially well known in peanuts, peas, and pansies, this behavior is most widespread in the grass family. However, the largest genus of cleistogamous plants is Viola . [1]

The more common opposite of cleistogamy, or "closed marriage", is called chasmogamy, or "open marriage". Virtually all plants that produce cleistogamous flowers also produce chasmogamous ones. [2] The principal advantage of cleistogamy is that it requires fewer plant resources to produce seeds than does chasmogamy, because development of petals, nectar and large amounts of pollen is not required. This efficiency makes cleistogamy particularly useful for seed production on unfavorable sites or adverse conditions. Impatiens capensis, for example, has been observed to produce only cleistogamous flowers after being severely damaged by grazing and to maintain populations on unfavorable sites with only cleistogamous flowers. The obvious disadvantage of cleistogamy is that self-fertilization occurs, which may suppress the creation of genetically more fit plants. [2] Another disadvantage of self-fertilization is that it leads to the expression in progeny of deleterious recessive mutations. [3]

For genetically modified (GM) rapeseed, researchers hoping to minimise the admixture of GM and non-GM crops are attempting to use cleistogamy to prevent gene flow. However, preliminary results from Co-Extra, a current project within the EU research program, show that although cleistogamy reduces gene flow, it is not at the moment a consistently reliable tool for biocontainment; due to a certain instability of the cleistogamous trait, some flowers may open and release genetically modified pollen. [4]

See also

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Reproductive 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.. This phenomenon has been observed since the 19th century, when Darwin observed that self-pollination was common in some plants. Constant pollen limitation may cause the evolution of automatic selfing, also known as autogamy. This occurs in plants such as weeds, and is a form of reproductive assurance. As plants pursue reproductive assurance through self-fertilization, there is an increase in homozygosity, and inbreeding depression, due to genetic load, which results in reduced fitness of selfed offspring. Solely outcrossing plants may not be successful colonizers of new regions due to lack of other plants to outcross with, so colonizing species are expected to have mechanisms of reproductive assurance - an idea first proposed by Herbert G. Baker and referred to as Baker's "law" or "rule". Baker's law predicts that reproductive assurance affects establishment of plants in many contexts, including spread by weedy plants and following long-distance dispersal, such as occurs during island colonization. As plants evolve towards increase self-fertilization, energy is redirected to seed production rather than characteristics that increased outcrossing, such as floral attractants, which is a condition known as the selfing syndrome.

References

  1. Sternberger, Anne L.; Ruhil, Anirudh V. S.; Rosenthal, David M.; Ballard, Harvey E.; Wyatt, Sarah E. (2020-03-11). "Environmental impact on the temporal production of chasmogamous and cleistogamous flowers in the mixed breeding system of Viola pubescens". PLOS ONE. 15 (3): e0229726. Bibcode:2020PLoSO..1529726S. doi: 10.1371/journal.pone.0229726 . ISSN   1932-6203. PMC   7065761 . PMID   32160228.
  2. 1 2 Meeuse, Bastiaan and Sean Morris. 1984. The sex life of flowers. New York, NY: Facts on File Publishers. pp 110-111.
  3. Bernstein, H.; Byerly, H. C.; Hopf, F. A.; Michod, R. E. (1985). "Genetic damage, mutation, and the evolution of sex". Science. 229 (4719): 1277–1281. Bibcode:1985Sci...229.1277B. doi:10.1126/science.3898363. PMID   3898363.
  4. "Co-Extra Projects : Biological methods for mitigating gene flow in rapeseed". 2011-07-20. Archived from the original on 2011-07-20. Retrieved 2022-07-26.{{cite web}}: CS1 maint: bot: original URL status unknown (link)