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Gynodioecy

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maternally inherited. Research done on plants has shown that hermaphroditic plants are in constant battles against organelle genes trying to kill their male parts. In over 140 plant species, these “male killer” genes have been observed. Male sterility genes cause plants to grow anthers that are stunted or withered and as a result, do not produce pollen. In most plants, there are nuclear fertility restoring genes that counteract the work of the male sterility genes, maintaining the hermaphroditic state of the plant. However, in some species of plants, the male sterility genes win the battle over the nuclear fertility restoring genes, and gynodioecy occurs.
31: 182:. Research has shown that a species can be either gynodioecious or self-incompatible, but very rarely is there a co-occurrence between the two. Therefore, gynodioecy and self-incompatibility tend to prevent each other's maintenance. Self-incompatibility of plants helps maintain androdioecy in plants, since males are in competition with only hermaphrodites to fertilize ovules. Self-incompatibility leads to a loss in gynodioecy, since neither hermaphrodites nor females have to deal with 313: 224: 209:
farmers take advantage of gynodioecy to produce favorable hybrid maize seeds. The farmers deliberately make use of the gynodioecy that develops in the maize, resulting in a population of male-sterile and female-fertile individuals. They then introduce a new strain of male-sterile individuals and the
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Two scenarios have been proposed to explain the evolutionary dynamics of the maintenance of gynodioecy. The first scenario, known as the balancing selection theory, considers the genetic factors that control gynodioecy over long evolutionary time scales. The balancing selection leads to cycles that
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Gynodioecy occurs as a result of a genetic mutation that inhibits a hermaphroditic plant from producing pollen, while keeping the female reproductive parts intact. Gynodioecy is extremely rare, with fewer than 1% of angiosperm species exhibiting the breeding system. Some notable taxa that exhibit a
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Theoretically, hermaphrodites should have the evolutionary and reproductive advantage over females in a population because they naturally can produce more offspring. Hermaphrodites can transmit their genes through both pollen and ovules, whereas females can only transmit genes via ovules. Thus, in
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explain the normal sex ratios in gynodioecious populations. The second scenario, known as epidemic dynamics, involves the arrival and loss of new cytoplasmic male sterility genes in new populations. These are the same genes that invade hermaphrodite populations and eventually result in gynodioecy.
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Sakai AK, Weller SG, Chen ML, Chou SY, Tasanont C. Evolution of gynodioecy and maintenance of females: The role of inbreeding depression, outcrossing rates, and resource allocation in Schiedea adamantis (Caryophyllaceae). Evolution. 1997 Jun;51(3):724-736. doi: 10.1111/j.1558-5646.1997.tb03656.x.
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It would appear that gynodioecy should not persist. In order for it to be maintained, the females need to have some sort of a reproductive advantage over the hermaphroditic population, known as female compensation or female advantage. Female advantage includes an increase in saved energy from not
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Cytoplasmic male sterility genes, usually found in the mitochondrial genome, show up and are established when female fertility is just slightly more than the hermaphroditic fertility. The female only needs to make slightly more or better seeds than hermaphrodites since the mitochondrial genome is
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when compared with woody lineages. Herbaceous growth form is also associated with a reduced pollen limitation and increased self-fertilization. A reduced pollen limitation may decrease seed quantity and quality. Woody growth form Lamiaceae are more pollen-limited and thus produce fewer seeds and
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Gynodioecy is a rare, but widely distributed sexual system in angiosperm species. Gynodioecy is found in at least 81 different angiosperm families but less than 1% of the angiosperms species on Earth are gynodioecious. One likely explanation for its rarity is due to its limited evolution. Since
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Gynodioecy is determined as a result of a genetic mutation that stops a plant from producing pollen, but still allows normal female reproductive features. In plants, nuclear genes are inherited from both parents, but all the cytoplasmic genes come from the mother. This allows male gametes to be
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Gynodioecy can evolve from hermaphroditism due to certain environmental factors. If enough resources in a population are allocated to the female functions in a hermaphroditic species, gynodioecy will ensue. On the other hand, if more of those resources favor a hermaphrodite's male functions,
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The reason for this variation in the rarity of gynodioecy stems from certain phenotypic traits or ecological factors that promote and favor the presence of female plants in a population. For example, a herbaceous growth form is much more highly favored in gynodioecious species of
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females are at a disadvantage when compared with hermaphrodites, they will never be able to evolve as quickly. In addition, gynodioecy is rare because the mechanisms that favor females and cause gynodioecy in some populations only operate in some plant lineages, but not others.
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producing pollen and making seedlings of higher quality, since hermaphrodite seedlings are susceptible to homozygous deleterious alleles. Additional advantages include more flowers, higher fruit set, higher total seed production, heavier seeds, and better germination rates.
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Gynodioecy is often referred to as the evolutionary intermediate state between hermaphroditism and dioecy, however there is no evidence it is an intermediate state in animals. Gynodioecy has been investigated by biologists dating as far back as to
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in a population facilitates the maintenance of gynodioecy by increasing the inbreeding costs for hermaphrodites. Thus, as the rate of inbreeding increases in a population, the more likely gynodioecy is to occur.
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seeds of lower quality, thus favoring the female herbaceous growth form. Gynodioecy is rare because some sexual systems are more evolutionarily liable to change in certain lineages in comparison with others.
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smaller and more motile while female gametes are larger. It makes sense for most plants to be hermaphrodites, since they are sessile and unable to find mates as easily as animals can.
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that is found in certain flowering plant species in which female and hermaphroditic plants coexist within a population. Gynodioecy is the evolutionary intermediate between
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Van de Paer C, Saumitou-Laprade P, Vernet P, Billiard S (April 2015). "The joint evolution and maintenance of self-incompatibility with gynodioecy or androdioecy".
1045:"Potential Ecological Constraints on the Evolution of Gynodioecy in Mimulus guttatus: Relative Fecundity and Pollinator Behavior in a Mixed-Sex Population" 323: 234: 610: 534: 1143: 884: 701:
Sinclair JP, Kameyama Y, Shibata A, Kudo G (September 2016). "Male-biased hermaphrodites in a gynodioecious shrub, Daphne jezoensis".
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order for females to remain viable in a population, they would have to be twice as successful as hermaphrodites.
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Delph LF, Touzet P, Bailey MF (January 2007). "Merging theory and mechanism in studies of gynodioecy".
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The following species and higher taxa have been observed to exhibit a gynodioecious breeding system:
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was found to be an important factor in the maintenance of gynodioecy in an endemic Hawaiian shrub
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occurring in a single population in Diamond Head Crater Oahu. Inbreeding depression, due to
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Hermaphroditic plants may be able to reproduce on their own but in many species they are
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Embryology of Flowering Plants: Terminology and Concepts, Vol. 3: Reproductive Systems
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breeders are able to collect the more favorable hybrid seeds.
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is an example of a species with a gynodioecious mating system.
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Coexistence of female and hermaphrodite within a population
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Torices, Rubén; Méndez, Marcos; Gómez, José María (2011).
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It has been estimated that gynodioecy occurs in 13.3% of
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Casimiro-Soriguer I, Buide ML, Narbona E (April 2015).
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The red queen: sex and the evolution of human nature
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The term was first used by 85:gynodioecious mating system include 632:Integrative and Comparative Biology 812:Preece T, Mao Y (September 2010). 322:relies largely or entirely upon a 233:relies largely or entirely upon a 25: 902:Trends in Ecology & Evolution 523:Fusco G, Minelli A (2019-10-10). 569:10.1111/j.1469-8137.2010.03609.x 311: 222: 153:Evolution of sexual reproduction 676:. In Marechal-Drouard L (ed.). 821:Journal of Theoretical Biology 779:Journal of Theoretical Biology 742:Journal of Experimental Botany 678:Mitochondrial genome evolution 599:Batygina, T. B. (2019-04-23). 1: 1043:Wise M, Vu J, Carr D (2011). 879:. Penguin. pp. 91–128. 170:will result. A high rate of 626:Leonard JL (October 2013). 526:The Biology of Reproduction 139:in 1877 when writing about 1165: 914:10.1016/j.tree.2006.09.013 841:10.1016/j.jtbi.2010.06.025 791:10.1016/j.jtbi.2015.02.003 150: 1144:Plant reproductive system 131:(twice or double), and 459:Cucurbita foetidissima 40: 999:10.1093/aobpla/plv037 383:Inbreeding depression 378:Inbreeding depression 184:inbreeding depression 33: 335:improve this article 246:improve this article 214:Species distribution 63:mixed mating systems 946:The New Phytologist 833:2010JThBi.266..219P 504:Erythranthe guttata 497:Reynoutria japonica 452:Fragaria virginiana 426:Lobelia siphilitica 417:Fuchsia excorticata 94:Lobelia siphilitica 36:Lobelia siphilitica 755:10.1093/jxb/erg007 645:10.1093/icb/ict088 388:Schiedea adamantis 41: 959:10.1111/nph.13926 875:Ridley M (1993). 715:10.1111/plb.12463 672:Touzet P (2012). 612:978-0-429-52671-8 536:978-1-108-49985-9 403:of small effect. 367: 366: 359: 278: 277: 270: 180:self-incompatible 16:(Redirected from 1156: 1088: 1087: 1085: 1083: 1040: 1034: 1030: 1021: 1020: 1010: 978: 972: 971: 961: 937: 926: 925: 897: 891: 890: 872: 861: 860: 818: 809: 803: 802: 774: 768: 767: 757: 733: 727: 726: 698: 692: 691: 669: 658: 657: 647: 623: 617: 616: 596: 590: 589: 571: 547: 541: 540: 520: 471:Daphne jezoensis 362: 355: 351: 348: 342: 315: 314: 307: 273: 266: 262: 259: 253: 226: 225: 218: 172:self-pollination 141:plant morphology 65:comparable with 21: 1164: 1163: 1159: 1158: 1157: 1155: 1154: 1153: 1129: 1128: 1096: 1091: 1081: 1079: 1042: 1041: 1037: 1031: 1024: 980: 979: 975: 939: 938: 929: 899: 898: 894: 887: 874: 873: 864: 816: 811: 810: 806: 776: 775: 771: 748:(380): 149–56. 735: 734: 730: 700: 699: 695: 688: 671: 670: 661: 625: 624: 620: 613: 598: 597: 593: 556:New Phytologist 549: 548: 544: 537: 522: 521: 517: 513: 478:Silene vulgaris 409: 380: 363: 352: 346: 343: 337:by introducing 328: 316: 312: 305: 274: 263: 257: 254: 248:by introducing 239: 227: 223: 216: 196: 155: 149: 113: 52:hermaphroditism 48:breeding system 28: 23: 22: 15: 12: 11: 5: 1162: 1160: 1152: 1151: 1146: 1141: 1131: 1130: 1127: 1126: 1125: 1124: 1119: 1114: 1109: 1104: 1095: 1092: 1090: 1089: 1069:10.1086/657677 1061:10.1086/657677 1055:(2): 199–210. 1035: 1022: 973: 927: 892: 886:978-0140167726 885: 862: 804: 769: 728: 693: 686: 659: 618: 611: 591: 562:(1): 234–248. 542: 535: 514: 512: 509: 508: 507: 500: 493: 488: 481: 474: 467: 462: 455: 448: 443: 436: 429: 421: 420: 408: 405: 397:hermaphrodites 379: 376: 365: 364: 333:. 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Index

Gynodioecious

Lobelia siphilitica
breeding system
hermaphroditism
dioecy
mixed mating systems
trioecy
androdioecy
dioecy
androdioecy
Beta vulgaris
Lobelia siphilitica
Silene
Lamiaceae
Greek
Charles Darwin
plant morphology
Evolution of sexual reproduction
Charles Darwin
androdioecy
self-pollination
self-incompatible
inbreeding depression
Maize
single source
talk page
improve this article
citations
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