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Self-pollination

Self-pollination is a form of pollination in which pollen from the same plant arrives at the stigma of a flower (in flowering plants) or at the ovule (in gymnosperms). There are two types of self-pollination: in autogamy, pollen is transferred to the stigma of the same flower; in geitonogamy, pollen is transferred from the anther of one flower to the stigma of another flower on the same flowering plant, or from microsporangium to ovule within a single (monoecious) gymnosperm. Some plants have mechanisms that ensure autogamy, such as flowers that do not open (cleistogamy), or stamens that move to come into contact with the stigma. The term selfing that is often used as a synonym, is not limited to self-pollination, but also applies to other type of self-fertilization.

One type of automatic self-pollination occurs in the orchid Ophrys apifera. One of the two pollinia bends itself towards the stigma.

Occurrence edit

Few plants self-pollinate without the aid of pollen vectors (such as wind or insects). The mechanism is seen most often in some legumes such as peanuts. In another legume, soybeans, the flowers open and remain receptive to insect cross pollination during the day. If this is not accomplished, the flowers self-pollinate as they are closing. Among other plants that can self-pollinate are many kinds of orchids, peas, sunflowers and tridax. Most of the self-pollinating plants have small, relatively inconspicuous flowers that shed pollen directly onto the stigma, sometimes even before the bud opens. Self-pollinated plants expend less energy in the production of pollinator attractants and can grow in areas where the kinds of insects or other animals that might visit them are absent or very scarce—as in the Arctic or at high elevations.

Self-pollination limits the variety of progeny and may depress plant vigor. However, self-pollination can be advantageous, allowing plants to spread beyond the range of suitable pollinators or produce offspring in areas where pollinator populations have been greatly reduced or are naturally variable.[1]

Pollination can also be accomplished by cross-pollination. Cross-pollination is the transfer of pollen, by wind or animals such as insects and birds, from the anther to the stigma of flowers on separate plants.

Types of self-pollinating flowers edit

Both hermaphrodite and monoecious species have the potential for self-pollination leading to self-fertilization unless there is a mechanism to avoid it. 80% of all flowering plants are hermaphroditic, meaning they contain both sexes in the same flower, while 5 percent of plant species are monoecious. The remaining 15% would therefore be dioecious (each plant unisexual). Plants that self-pollinate include several types of orchids, and sunflowers. Dandelions are capable of self-pollination as well as cross-pollination.

Advantages edit

There are several advantages for self-pollinating flowers. Firstly, if a given genotype is well-suited for an environment, self-pollination helps to keep this trait stable in the species. Not being dependent on pollinating agents allows self-pollination to occur when bees and wind are nowhere to be found. Self-pollination or cross pollination can be an advantage when the number of flowers is small or they are widely spaced. During self-pollination, the pollen grains are not transmitted from one flower to another. As a result, there is less wastage of pollen. Also, self-pollinating plants do not depend on external carriers. They also cannot make changes in their characters and so the features of a species can be maintained with purity. Self-pollination also helps to preserve parental characters as the gametes from the same flower are evolved. It is not necessary for flowers to produce nectar, scent, or to be colourful in order to attract pollinators.

Disadvantages edit

The disadvantages of self-pollination come from a lack of variation that allows no adaptation to the changing environment or potential pathogen attack. Self-pollination can lead to inbreeding depression caused by expression of deleterious recessive mutations,[2] or to the reduced health of the species, due to the breeding of related specimens. This is why many flowers that could potentially self-pollinate have a built-in mechanism to avoid it, or make it second choice at best. Genetic defects in self-pollinating plants cannot be eliminated by genetic recombination and offspring can only avoid inheriting the deleterious attributes through a chance mutation arising in a gamete.

Mixed mating edit

About 42% of flowering plants exhibit a mixed mating system in nature.[3] In the most common kind of system, individual plants produce a single flower type and fruits may contain self-pollinated, out-crossed or a mixture of progeny types. Another mixed mating system is referred to as dimorphic cleistogamy. In this system a single plant produces both open, potentially out-crossed and closed, obligately self-pollinated cleistogamous flowers.[4]

Example species edit

The evolutionary shift from outcrossing to self-fertilization is one of the most common evolutionary transitions in plants. About 10-15% of flowering plants are predominantly self-fertilizing.[5] A few well-studied examples of self-pollinating species are described below.

Orchids edit

Self-pollination in the slipper orchid Paphiopedilum parishii occurs when the anther changes from a solid to a liquid state and directly contacts the stigma surface without the aid of any pollinating agent.[6]

The tree-living orchid Holcoglossum amesianum has a type of self-pollination mechanism in which the bisexual flower turns its anther against gravity through 360° in order to insert pollen into its own stigma cavity—without the aid of any pollinating agent or medium. This type of self-pollination appears to be an adaptation to the windless, drought conditions that are present when flowering occurs, at a time when insects are scarce.[7] Without pollinators for outcrossing, the necessity of ensuring reproductive success appears to outweigh potential adverse effects of inbreeding. Such an adaptation may be widespread among species in similar environments.

Self-pollination in the Madagascan orchid Bulbophyllum bicoloratum occurs by virtue of a rostellum that may have regained its stigmatic function as part of the distal median stigmatic lobe.[8]

Caulokaempferia coenobialis edit

In the Chinese herb Caulokaempferia coenobialis a film of pollen is transported from the anther (pollen sacs) by an oily emulsion that slides sideways along the flower's style and into the individual's own stigma.[9] The lateral flow of the film of pollen along the style appears to be due solely to the spreading properties of the oily emulsion and not to gravity. This strategy may have evolved to cope with a scarcity of pollinators in the extremely shady and humid habitats of C. coenobialis.

Capsella rubella edit

Capsella rubella (Red Shepard's purse)[10][11] is a self-pollinating species that became self-compatible 50,000 to 100,000 years ago, indicating that self-pollination is an evolutionary adaptation that can persist over many generations. Its out-crossing progenitor was identified as Capsella grandiflora.

Arabidopsis thaliana edit

Arabidopsis thaliana is a predominantly self-pollinating plant with an out-crossing rate in the wild estimated at less than 0.3%.[12] A study suggested that self-pollination evolved roughly a million years ago or more.[13]

Possible long-term benefit of meiosis edit

Meiosis followed by self-pollination produces little overall genetic variation. This raises the question of how meiosis in self-pollinating plants is adaptively maintained over extended periods (i.e. for roughly a million years or more, as in the case of A. thaliana)[13] in preference to a less complicated and less costly asexual ameiotic process for producing progeny. An adaptive benefit of meiosis that may explain its long-term maintenance in self-pollinating plants is efficient recombinational repair of DNA damage.[14] This benefit can be realized at each generation (even when genetic variation is not produced).

See also edit

References edit

  1. ^ Grossenbacher D, Briscoe Runquist R, Goldberg EE, Brandvain Y (2015). "Geographic range size is predicted by plant mating system". Ecol. Lett. 18 (7): 706–13. doi:10.1111/ele.12449. PMID 25980327. S2CID 833417.
  2. ^ Charlesworth D, Willis JH (2009). "The genetics of inbreeding depression". Nat. Rev. Genet. 10 (11): 783–96. doi:10.1038/nrg2664. PMID 19834483. S2CID 771357.
  3. ^ Goodwillie C, Kalisz S, Eckert CG (2005). "The evolutionary enigma of mixed mating systems in plants: Occurrence, theoretical explanations, and empirical evidence". Annu. Rev. Ecol. Evol. Syst. 36: 47–79. doi:10.1146/annurev.ecolsys.36.091704.175539.
  4. ^ Munguía-Rosas MA, Campos-Navarrete MJ, Parra-Tabla V (2013). "The effect of pollen source vs. flower type on progeny performance and seed predation under contrasting light environments in a cleistogamous herb". PLOS ONE. 8 (11): e80934. Bibcode:2013PLoSO...880934M. doi:10.1371/journal.pone.0080934. PMC 3829907. PMID 24260515.
  5. ^ Wright SI, Kalisz S, Slotte T (June 2013). "Evolutionary consequences of self-fertilization in plants". Proc. Biol. Sci. 280 (1760): 20130133. doi:10.1098/rspb.2013.0133. PMC 3652455. PMID 23595268.
  6. ^ Chen LJ, Liu KW, Xiao XJ, Tsai WC, Hsiao YY, Huang J, Liu ZJ (2012). "The anther steps onto the stigma for self-fertilization in a slipper orchid". PLOS ONE. 7 (5): e37478. Bibcode:2012PLoSO...737478C. doi:10.1371/journal.pone.0037478. PMC 3359306. PMID 22649529.
  7. ^ Liu KW, Liu ZJ, Huang L, Li LQ, Chen LJ, Tang GD (June 2006). "Pollination: self-fertilization strategy in an orchid". Nature. 441 (7096): 945–6. Bibcode:2006Natur.441..945L. doi:10.1038/441945a. PMID 16791185. S2CID 4382904.
  8. ^ Gamisch A, Staedler YM, Schönenberger J, Fischer GA, Comes HP (2013). "Histological and Micro-CT Evidence of Stigmatic Rostellum Receptivity Promoting Auto-Pollination in the Madagascan Orchid Bulbophyllum bicoloratum". PLOS ONE. 8 (8): e72688. Bibcode:2013PLoSO...872688G. doi:10.1371/journal.pone.0072688. PMC 3742538. PMID 23967332. S2CID 5787057.
  9. ^ Wang Y, Zhang D, Renner SS, Chen Z (September 2004). "Botany: a new self-pollination mechanism". Nature. 431 (7004): 39–40. Bibcode:2004Natur.431...39W. doi:10.1038/431039b. PMID 15343325. S2CID 52858044.
  10. ^ Brandvain Y, Slotte T, Hazzouri KM, Wright SI, Coop G (2013). "Genomic identification of founding haplotypes reveals the history of the selfing species Capsella rubella". PLOS Genet. 9 (9): e1003754. arXiv:1307.4118. doi:10.1371/journal.pgen.1003754. PMC 3772084. PMID 24068948.
  11. ^ Slotte T, Hazzouri KM, Ågren JA, Koenig D, Maumus F, Guo YL, Steige K, Platts AE, Escobar JS, Newman LK, Wang W, Mandáková T, Vello E, Smith LM, Henz SR, Steffen J, Takuno S, Brandvain Y, Coop G, Andolfatto P, Hu TT, Blanchette M, Clark RM, Quesneville H, Nordborg M, Gaut BS, Lysak MA, Jenkins J, Grimwood J, Chapman J, Prochnik S, Shu S, Rokhsar D, Schmutz J, Weigel D, Wright SI (July 2013). "The Capsella rubella genome and the genomic consequences of rapid mating system evolution". Nat. Genet. 45 (7): 831–5. doi:10.1038/ng.2669. PMID 23749190.
  12. ^ Abbott RJ, Gomes MF (1989). "Population genetic structure and outcrossing rate of Arabidopsis thaliana (L.) Heynh". Heredity. 62 (3): 411–418. doi:10.1038/hdy.1989.56. S2CID 41914710.
  13. ^ a b Tang C, Toomajian C, Sherman-Broyles S, Plagnol V, Guo YL, Hu TT, Clark RM, Nasrallah JB, Weigel D, Nordborg M (August 2007). "The evolution of selfing in Arabidopsis thaliana". Science. 317 (5841): 1070–2. Bibcode:2007Sci...317.1070T. doi:10.1126/science.1143153. PMID 17656687. S2CID 45853624.
  14. ^ Bernstein H, Hopf FA, Michod RE (1987). "The molecular basis of the evolution of sex". Adv Genet. Advances in Genetics. 24: 323–70. doi:10.1016/s0065-2660(08)60012-7. ISBN 9780120176243. PMID 3324702.

self, pollination, form, pollination, which, pollen, from, same, plant, arrives, stigma, flower, flowering, plants, ovule, gymnosperms, there, types, self, pollination, autogamy, pollen, transferred, stigma, same, flower, geitonogamy, pollen, transferred, from. Self pollination is a form of pollination in which pollen from the same plant arrives at the stigma of a flower in flowering plants or at the ovule in gymnosperms There are two types of self pollination in autogamy pollen is transferred to the stigma of the same flower in geitonogamy pollen is transferred from the anther of one flower to the stigma of another flower on the same flowering plant or from microsporangium to ovule within a single monoecious gymnosperm Some plants have mechanisms that ensure autogamy such as flowers that do not open cleistogamy or stamens that move to come into contact with the stigma The term selfing that is often used as a synonym is not limited to self pollination but also applies to other type of self fertilization One type of automatic self pollination occurs in the orchid Ophrys apifera One of the two pollinia bends itself towards the stigma Contents 1 Occurrence 2 Types of self pollinating flowers 3 Advantages 4 Disadvantages 5 Mixed mating 6 Example species 6 1 Orchids 6 2 Caulokaempferia coenobialis 6 3 Capsella rubella 6 4 Arabidopsis thaliana 7 Possible long term benefit of meiosis 8 See also 9 ReferencesOccurrence editFew plants self pollinate without the aid of pollen vectors such as wind or insects The mechanism is seen most often in some legumes such as peanuts In another legume soybeans the flowers open and remain receptive to insect cross pollination during the day If this is not accomplished the flowers self pollinate as they are closing Among other plants that can self pollinate are many kinds of orchids peas sunflowers and tridax Most of the self pollinating plants have small relatively inconspicuous flowers that shed pollen directly onto the stigma sometimes even before the bud opens Self pollinated plants expend less energy in the production of pollinator attractants and can grow in areas where the kinds of insects or other animals that might visit them are absent or very scarce as in the Arctic or at high elevations Self pollination limits the variety of progeny and may depress plant vigor However self pollination can be advantageous allowing plants to spread beyond the range of suitable pollinators or produce offspring in areas where pollinator populations have been greatly reduced or are naturally variable 1 Pollination can also be accomplished by cross pollination Cross pollination is the transfer of pollen by wind or animals such as insects and birds from the anther to the stigma of flowers on separate plants Types of self pollinating flowers editBoth hermaphrodite and monoecious species have the potential for self pollination leading to self fertilization unless there is a mechanism to avoid it 80 of all flowering plants are hermaphroditic meaning they contain both sexes in the same flower while 5 percent of plant species are monoecious The remaining 15 would therefore be dioecious each plant unisexual Plants that self pollinate include several types of orchids and sunflowers Dandelions are capable of self pollination as well as cross pollination Advantages editThere are several advantages for self pollinating flowers Firstly if a given genotype is well suited for an environment self pollination helps to keep this trait stable in the species Not being dependent on pollinating agents allows self pollination to occur when bees and wind are nowhere to be found Self pollination or cross pollination can be an advantage when the number of flowers is small or they are widely spaced During self pollination the pollen grains are not transmitted from one flower to another As a result there is less wastage of pollen Also self pollinating plants do not depend on external carriers They also cannot make changes in their characters and so the features of a species can be maintained with purity Self pollination also helps to preserve parental characters as the gametes from the same flower are evolved It is not necessary for flowers to produce nectar scent or to be colourful in order to attract pollinators Disadvantages editThe disadvantages of self pollination come from a lack of variation that allows no adaptation to the changing environment or potential pathogen attack Self pollination can lead to inbreeding depression caused by expression of deleterious recessive mutations 2 or to the reduced health of the species due to the breeding of related specimens This is why many flowers that could potentially self pollinate have a built in mechanism to avoid it or make it second choice at best Genetic defects in self pollinating plants cannot be eliminated by genetic recombination and offspring can only avoid inheriting the deleterious attributes through a chance mutation arising in a gamete Mixed mating editAbout 42 of flowering plants exhibit a mixed mating system in nature 3 In the most common kind of system individual plants produce a single flower type and fruits may contain self pollinated out crossed or a mixture of progeny types Another mixed mating system is referred to as dimorphic cleistogamy In this system a single plant produces both open potentially out crossed and closed obligately self pollinated cleistogamous flowers 4 Example species editThe evolutionary shift from outcrossing to self fertilization is one of the most common evolutionary transitions in plants About 10 15 of flowering plants are predominantly self fertilizing 5 A few well studied examples of self pollinating species are described below Orchids edit Self pollination in the slipper orchid Paphiopedilum parishii occurs when the anther changes from a solid to a liquid state and directly contacts the stigma surface without the aid of any pollinating agent 6 The tree living orchid Holcoglossum amesianum has a type of self pollination mechanism in which the bisexual flower turns its anther against gravity through 360 in order to insert pollen into its own stigma cavity without the aid of any pollinating agent or medium This type of self pollination appears to be an adaptation to the windless drought conditions that are present when flowering occurs at a time when insects are scarce 7 Without pollinators for outcrossing the necessity of ensuring reproductive success appears to outweigh potential adverse effects of inbreeding Such an adaptation may be widespread among species in similar environments Self pollination in the Madagascan orchid Bulbophyllum bicoloratum occurs by virtue of a rostellum that may have regained its stigmatic function as part of the distal median stigmatic lobe 8 Caulokaempferia coenobialis edit In the Chinese herb Caulokaempferia coenobialis a film of pollen is transported from the anther pollen sacs by an oily emulsion that slides sideways along the flower s style and into the individual s own stigma 9 The lateral flow of the film of pollen along the style appears to be due solely to the spreading properties of the oily emulsion and not to gravity This strategy may have evolved to cope with a scarcity of pollinators in the extremely shady and humid habitats of C coenobialis Capsella rubella edit Capsella rubella Red Shepard s purse 10 11 is a self pollinating species that became self compatible 50 000 to 100 000 years ago indicating that self pollination is an evolutionary adaptation that can persist over many generations Its out crossing progenitor was identified as Capsella grandiflora Arabidopsis thaliana edit Arabidopsis thaliana is a predominantly self pollinating plant with an out crossing rate in the wild estimated at less than 0 3 12 A study suggested that self pollination evolved roughly a million years ago or more 13 Possible long term benefit of meiosis editMeiosis followed by self pollination produces little overall genetic variation This raises the question of how meiosis in self pollinating plants is adaptively maintained over extended periods i e for roughly a million years or more as in the case of A thaliana 13 in preference to a less complicated and less costly asexual ameiotic process for producing progeny An adaptive benefit of meiosis that may explain its long term maintenance in self pollinating plants is efficient recombinational repair of DNA damage 14 This benefit can be realized at each generation even when genetic variation is not produced See also editSelf incompatibility genetic mechanisms which prevent self fertilization Reproduction Monocotyledon reproductionReferences edit Grossenbacher D Briscoe Runquist R Goldberg EE Brandvain Y 2015 Geographic range size is predicted by plant mating system Ecol Lett 18 7 706 13 doi 10 1111 ele 12449 PMID 25980327 S2CID 833417 Charlesworth D Willis JH 2009 The genetics of inbreeding depression Nat Rev Genet 10 11 783 96 doi 10 1038 nrg2664 PMID 19834483 S2CID 771357 Goodwillie C Kalisz S Eckert CG 2005 The evolutionary enigma of mixed mating systems in plants Occurrence theoretical explanations and empirical evidence Annu Rev Ecol Evol Syst 36 47 79 doi 10 1146 annurev ecolsys 36 091704 175539 Munguia Rosas MA Campos Navarrete MJ Parra Tabla V 2013 The effect of pollen source vs flower type on progeny performance and seed predation under contrasting light environments in a cleistogamous herb PLOS ONE 8 11 e80934 Bibcode 2013PLoSO 880934M doi 10 1371 journal pone 0080934 PMC 3829907 PMID 24260515 Wright SI Kalisz S Slotte T June 2013 Evolutionary consequences of self fertilization in plants Proc Biol Sci 280 1760 20130133 doi 10 1098 rspb 2013 0133 PMC 3652455 PMID 23595268 Chen LJ Liu KW Xiao XJ Tsai WC Hsiao YY Huang J Liu ZJ 2012 The anther steps onto the stigma for self fertilization in a slipper orchid PLOS ONE 7 5 e37478 Bibcode 2012PLoSO 737478C doi 10 1371 journal pone 0037478 PMC 3359306 PMID 22649529 Liu KW Liu ZJ Huang L Li LQ Chen LJ Tang GD June 2006 Pollination self fertilization strategy in an orchid Nature 441 7096 945 6 Bibcode 2006Natur 441 945L doi 10 1038 441945a PMID 16791185 S2CID 4382904 Gamisch A Staedler YM Schonenberger J Fischer GA Comes HP 2013 Histological and Micro CT Evidence of Stigmatic Rostellum Receptivity Promoting Auto Pollination in the Madagascan Orchid Bulbophyllum bicoloratum PLOS ONE 8 8 e72688 Bibcode 2013PLoSO 872688G doi 10 1371 journal pone 0072688 PMC 3742538 PMID 23967332 S2CID 5787057 Wang Y Zhang D Renner SS Chen Z September 2004 Botany a new self pollination mechanism Nature 431 7004 39 40 Bibcode 2004Natur 431 39W doi 10 1038 431039b PMID 15343325 S2CID 52858044 Brandvain Y Slotte T Hazzouri KM Wright SI Coop G 2013 Genomic identification of founding haplotypes reveals the history of the selfing species Capsella rubella PLOS Genet 9 9 e1003754 arXiv 1307 4118 doi 10 1371 journal pgen 1003754 PMC 3772084 PMID 24068948 Slotte T Hazzouri KM Agren JA Koenig D Maumus F Guo YL Steige K Platts AE Escobar JS Newman LK Wang W Mandakova T Vello E Smith LM Henz SR Steffen J Takuno S Brandvain Y Coop G Andolfatto P Hu TT Blanchette M Clark RM Quesneville H Nordborg M Gaut BS Lysak MA Jenkins J Grimwood J Chapman J Prochnik S Shu S Rokhsar D Schmutz J Weigel D Wright SI July 2013 The Capsella rubella genome and the genomic consequences of rapid mating system evolution Nat Genet 45 7 831 5 doi 10 1038 ng 2669 PMID 23749190 Abbott RJ Gomes MF 1989 Population genetic structure and outcrossing rate of Arabidopsis thaliana L Heynh Heredity 62 3 411 418 doi 10 1038 hdy 1989 56 S2CID 41914710 a b Tang C Toomajian C Sherman Broyles S Plagnol V Guo YL Hu TT Clark RM Nasrallah JB Weigel D Nordborg M August 2007 The evolution of selfing in Arabidopsis thaliana Science 317 5841 1070 2 Bibcode 2007Sci 317 1070T doi 10 1126 science 1143153 PMID 17656687 S2CID 45853624 Bernstein H Hopf FA Michod RE 1987 The molecular basis of the evolution of sex Adv Genet Advances in Genetics 24 323 70 doi 10 1016 s0065 2660 08 60012 7 ISBN 9780120176243 PMID 3324702 Retrieved from https en wikipedia org w index php title Self pollination amp oldid 1184620498, wikipedia, wiki, book, books, library,

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