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Journal articles on the topic 'Cleistogamy'

Author: Grafiati

Published: 4 June 2021

Last updated: 26 July 2025

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1

Ammarellou, Ali, Justyna Żabicka, Aneta Słomka, Jerzy Bohdanowicz, Thomas Marcussen, and Elżbieta Kuta. "Seasonal and Simultaneous Cleistogamy in Rostrate Violets (Viola, subsect. Rostratae, Violaceae)." Plants 10, no. 10 (2021): 2147. http://dx.doi.org/10.3390/plants10102147.

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The special mixed reproductive system, i.e., the ability of an individual plant to develop both open, chasmogamous (CH) flowers adapted to cross-pollination and closed, cleistogamous (CL) flowers with obligate self-pollinating, is a common phenomenon in Viola L. In most sections of Northern Hemisphere violets, cleistogamy is seasonal, and CH and CL flowers develop sequentially in the season. Non-seasonal cleistogamy (simultaneous) is a rare phenomenon in rostrate violets. In the current study, we focused on modification of the CH/CL mating system in V. caspia by environmental conditions, resul

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2

Kulkarni, R. N., and K. Baskaran. "From Herkogamy to Cleistogamy - Development of Cleistogamy in Periwinkle." Journal of Heredity 104, no. 1 (2012): 140–48. http://dx.doi.org/10.1093/jhered/ess077.

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3

Wu, Minliang, Xinxin Bian, Benben Huang, et al. "HD-Zip proteins modify floral structures for self-pollination in tomato." Science 384, no. 6691 (2024): 124–30. http://dx.doi.org/10.1126/science.adl1982.

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Cleistogamy is a type of self-pollination that relies on the formation of a stigma-enclosing floral structure. We identify three homeodomain-leucine zipper IV (HD-Zip IV) genes that coordinately promote the formation of interlocking trichomes at the anther margin to unite neighboring anthers, generating a closed anther cone and cleistogamy (flower morphology necessitating strict self-pollination). These HD-Zip IV genes also control style length by regulating the transition from cell division to endoreduplication. The expression of these HD-Zip IV genes and their downstream gene, Style 2.1 , wa

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4

Mattila, Tanja, and Veikko Salonen. "Reproduction of Viola mirabilis in relation to light and nutrient availability." Canadian Journal of Botany 73, no. 12 (1995): 1917–24. http://dx.doi.org/10.1139/b95-204.

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Mixed mating strategies in plants, such as chasmogamy and cleistogamy, may have evolved to optimize reproductive response to local, often variable, environmental conditions. A 2-year field experiment was conducted to examine the effects of light and nutrient availability on growth and chasmogamous and cleistogamous flower and fruit production in Viola mirabilis, a perennial forest understory herb. Using a factorial design, we examined whether the mode of reproduction or reproductive output of V. mirabilis would be influenced by a repeated fertilizer application and (or) gradual shading with ar

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5

Wang, Lijuan, Nian-Oine Shi, Murray E. Duysen, and Chiwon W. Lee. "747 PB 105 CLEISTOGAMY GENE ACTION IN SALPIGLOSSIS IS LINKED TO SUGAR METABOLISM." HortScience 29, no. 5 (1994): 540b—540. http://dx.doi.org/10.21273/hortsci.29.5.540b.

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Cleistogamy in Salpiglossis sinuatu L. involves a sequence of events, including arrested corolla development, precocious pollen germination inside anther, pollen tube penetration of the pistil, and eventual self fertilization, that takes place. within a tightly closed flower bud. A single dominant gene (C) controls cleistogamy in this plant. During early blooming period, cleistogamous (CC, Cc) plants produce both chasmogamous (open) and cleistogamous (closed) flowers. Enzymes in various tissues of both cleistogamous and chasmogamous buds were detected by isozyme banding patterns in starch gel

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6

Giełwanowska, Irena, Ewa Szczuka, and Anna Bochenek. "Pollination in the Antarctic flowering plant Colobanthus quitensis (Kunth) Bartl." Acta Agrobotanica 59, no. 1 (2012): 123–31. http://dx.doi.org/10.5586/aa.2006.012.

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<i>Colobanthus quitensis</i> forms chasmogamic and cleistogamic flowers. Their structure signals the possibility of both cross-pollination and self-pollination. In favorable conditions (natural or laboratory), flowers open creating a possibility for cross-pollination. The occurrence of cleistogamy in the investigated species may be conditioned by abiotic factors: low temperature, high air humidity, and strong wind. In closed flowers, a part of pollen grains reaches the stigma surface, and the rest remains inside the microsporangium. Pollen grains germinate on the stigma surface or

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7

Gilmartin, A. J., and Gregory K. Brown. "Cleistogamy in Tillandsia capillaris (Bromeliaceae)." Biotropica 17, no. 3 (1985): 256. http://dx.doi.org/10.2307/2388227.

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8

Khosla, C., K. R. Shivanna, and H. Y. Mohan Ram. "Cleistogamy in Griffithella hookeriana (Podostemaceae)." South African Journal of Botany 67, no. 2 (2001): 320–24. http://dx.doi.org/10.1016/s0254-6299(15)31135-2.

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9

Tang, Caiguo, Huilan Zhang, Pingping Zhang, et al. "iTRAQ-based quantitative proteome analysis reveals metabolic changes between a cleistogamous wheat mutant and its wild-type wheat counterpart." PeerJ 7 (June 17, 2019): e7104. http://dx.doi.org/10.7717/peerj.7104.

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Background Wheat is one of the most important staple crops worldwide. Fusarium head blight (FHB) severely affects wheat yield and quality. A novel bread wheat mutant, ZK001, characterized as cleistogamic was isolated from a non-cleistogamous variety Yumai 18 (YM18) through static magnetic field mutagenesis. Cleistogamy is a promising strategy for controlling FHB. However, little is known about the mechanism of cleistogamy in wheat. Methods We performed a FHB resistance test to identify the FHB infection rate of ZK001. We also measured the agronomic traits of ZK001 and the starch and total solu

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10

Forrest, Jessica, and James D. Thomson. "Pollen limitation and cleistogamy in subalpine Viola praemorsa." Botany 86, no. 5 (2008): 511–19. http://dx.doi.org/10.1139/b08-020.

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Early-flowering species may be especially susceptible to occasional pollen limitation and, therefore, may benefit from a mixed-mating strategy that provides reproductive assurance. We studied cleistogamous (CL) and chasmogamous (CH) fruit set of spring-flowering Viola praemorsa Dougl. ex Lindl. along an elevational gradient in the Rocky Mountains, testing whether pollen limitation or allocation to CL reproduction covaried with timing of flowering onset, within and across sites. Contrary to predictions, we found no pollen limitation of reproduction at any site, and variation among sites in the

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11

Manivannan, A. "Prospects of Cleistogamy in Plant Breeding." Research Biotica 2, no. 3 (2020): 102. http://dx.doi.org/10.54083/resbio/2.3.2020.102-104.

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12

Khan, Nisar A., Stephen M. Githiri, Eduardo R. Benitez, et al. "QTL analysis of cleistogamy in soybean." Theoretical and Applied Genetics 117, no. 4 (2008): 479–87. http://dx.doi.org/10.1007/s00122-008-0792-5.

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13

Suetsugu, Kenji. "Gastrodia flexistyloides (Orchidaceae), a new mycoheterotrophic plant with complete cleistogamy from Japan." Phytotaxa 175, no. 5 (2014): 270–74. https://doi.org/10.11646/phytotaxa.175.5.5.

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Suetsugu, Kenji (2014): Gastrodia flexistyloides (Orchidaceae), a new mycoheterotrophic plant with complete cleistogamy from Japan. Phytotaxa 175 (5): 270-274, DOI: 10.11646/phytotaxa.175.5.5, URL: http://dx.doi.org/10.11646/phytotaxa.175.5.5

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14

DHAKAD, ASHOK, V. B. PATEL, S. K. SINGH, et al. "Pollen biology and metaxenic studies on early maturing grape (Vitis vinifera) genotypes." Indian Journal of Agricultural Sciences 94, no. 10 (2024): 1094–99. http://dx.doi.org/10.56093/ijas.v94i10.141725.

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The present experiment was conducted during 2020–21 and 2021–22 at ICAR-Indian Agricultural Research Institute, New Delhi to study the impact of open-, self-, and cross-pollination on metaxenic traits (berries) and the incidence of cleistogamy in grapes (Vitis vinifera L.). Seven different cross-combinations were used on the grape variety Pusa Navrang, which were planted at 3 m × 3 m spacing and trained on the Y-trellis training system. The experiment was laid out in a randomized block design (RBD) with four replications. The incidence of cleistogamy, berry set, retention percentage, and the m

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15

Thomas Philbrick, C., Milada Vomela, and Alejandro R. Novelo. "Preanthesis cleistogamy in the genus Podostemum (Podostemaceae)." Rhodora 108, no. 935 (2006): 195–202. http://dx.doi.org/10.3119/0035-4902(2006)108[195:pcitgp]2.0.co;2.

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16

Guerra, M. E., C. Casadomet, and J. Rodrigo. "Self-compatibility and cleistogamy in Japanese plum." Acta Horticulturae, no. 1342 (June 2022): 201–6. http://dx.doi.org/10.17660/actahortic.2022.1342.29.

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17

de Clavijo, E. Ruiz, and M. J. Jimenez. "Cleistogamy and Chasmogamy in Ceratocapnos heterocarpa (Fumariaceae)." International Journal of Plant Sciences 154, no. 2 (1993): 325–33. http://dx.doi.org/10.1086/297113.

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18

Wang, Ning, Shunzong Ning, Mohammad Pourkheirandish, Ichiro Honda, and Takao Komatsuda. "An alternative mechanism for cleistogamy in barley." Theoretical and Applied Genetics 126, no. 11 (2013): 2753–62. http://dx.doi.org/10.1007/s00122-013-2169-7.

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19

Ohmori, Shinnosuke, Setsuo Koike, Takami Hayashi, Tomoya Yamaguchi, Makoto Kuroki, and Hitoshi Yoshida. "The cleistogamy of the superwoman1-cleistogamy1 mutation is sensitive to low temperatures during the lodicule-forming stage." Breeding Science 68, no. 4 (2018): 432–41. http://dx.doi.org/10.1270/jsbbs.18028.

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20

Thompson, E. J. "A review of the classification and taxonomic and geographic distribution of cleistogamy in Australian grasses." Australian Journal of Botany 70, no. 1 (2021): 63–101. http://dx.doi.org/10.1071/bt20114.

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Cleistogamy, self-fertilisation within a closed flower, was found in 135 Australian grass species from 46 genera within 5 subfamilies representing 14% of the species and 30% of the genera. This represents an increase from 4% of species and 12% of genera from previous records. Expressions of cleistogamy were classified into three main categories on the basis of: presence or absence of anther dimorphism, presence of amphigamy with or without spikelet peculiarities, and chasmogamous and cleistogamous spikelets on separate plants. One category of these dimorphisms involves species that have differ

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21

Sauquet, Hervé. "Evolution: Cleistogamy to the rescue of zygomorphic flowers." Current Biology 31, no. 7 (2021): R332—R335. http://dx.doi.org/10.1016/j.cub.2021.01.054.

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22

Cheplick, Gregory P. "Cleistogamy and Seed Heteromorphism in Triplasis purpurea (Poaceae)." Bulletin of the Torrey Botanical Club 123, no. 1 (1996): 25. http://dx.doi.org/10.2307/2996303.

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23

Takahashi, R. "Genetic and Linkage Analysis of Cleistogamy in Soybean." Journal of Heredity 92, no. 1 (2001): 89–92. http://dx.doi.org/10.1093/jhered/92.1.89.

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24

Benitez, Eduardo R., Nisar A. Khan, Hisakazu Matsumura, Jun Abe, and Ryoji Takahashi. "Varietal Differences and Morphology of Cleistogamy in Soybean." Crop Science 50, no. 1 (2010): 185–90. http://dx.doi.org/10.2135/cropsci2009.02.0108.

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25

Turuspekov, Y., Y. Mano, I. Honda, N. Kawada, Y. Watanabe, and T. Komatsuda. "Identification and mapping of cleistogamy genes in barley." Theoretical and Applied Genetics 109, no. 3 (2004): 480–87. http://dx.doi.org/10.1007/s00122-004-1673-1.

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26

Goodwillie, Carol, and Emily Stewart. "Cleistogamy and Hybridization in Two Subspecies ofTriodanis perfoliata(Campanulaceae)." Rhodora 115, no. 961 (2013): 42–60. http://dx.doi.org/10.3119/12-01.

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27

Anwar, Nadia, Masaru Ohta, Takayuki Yazawa, et al. "miR172 downregulates the translation of cleistogamy 1 in barley." Annals of Botany 122, no. 2 (2018): 251–65. http://dx.doi.org/10.1093/aob/mcy058.

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28

Yoshida, Hitoshi, Shinnosuke Ohmori, Osamu Yatou, et al. "Cleistogamy in crops—molecular mechanism and utilization in breeding." Breeding Research 16, no. 2 (2014): 61–66. http://dx.doi.org/10.1270/jsbbr.16.61.

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29

Connor, H. E. "Breeding systems in New Zealand grasses XII. Cleistogamy inFestuca∗." New Zealand Journal of Botany 36, no. 3 (1998): 471–76. http://dx.doi.org/10.1080/0028825x.1998.9512585.

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30

REDBO-TORSTENSSON, PETER, and HENRIK BERG. "Seasonal cleistogamy: a conditional strategy to provide reproductive assurance." Acta Botanica Neerlandica 44, no. 3 (1995): 247–56. http://dx.doi.org/10.1111/j.1438-8677.1995.tb00783.x.

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31

Małobęcki, Andrzej, Thomas Marcussen, Jerzy Bohdanowicz, Grzegorz Migdałek, Aneta Słomka, and Elżbieta Kuta. "Cleistogamy and phylogenetic position ofViola uliginosa(Violaceae) re-examined." Botanical Journal of the Linnean Society 182, no. 1 (2016): 180–94. http://dx.doi.org/10.1111/boj.12460.

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32

Sharma, V. K., H. S. Ginwal, and A. K. Mandal. "Short Note: Cleistogamy in Eucalyptus tereticornis Sm. and its Genetic Implications." Silvae Genetica 54, no. 1-6 (2005): 46–47. http://dx.doi.org/10.1515/sg-2005-0008.

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Abstract In a provenance cum progeny trial comprising 13 provenances and 91 families of Eucalyptus tereticornis Sm. of Australian and Papua New Guinean (PNG) origin, laid out in India in 2002, cleistogamy was found in a family emanating from CSIRO seed lot no. 13418, (tree no. DS000141) Sirinumu Sogeri Plat, PNG. This trait appears to be under genetic control, and presumably results in obligate selfing. This may lead to inbreeding depression in this family.

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33

DARBYSHIRE, S. J., and J. CAYOUETTE. "THE BIOLOGY OF CANADIAN WEEDS.: 92. Danthonia spicata (L.) BEAUV. IN ROEM. & SCHULT." Canadian Journal of Plant Science 69, no. 4 (1989): 1217–33. http://dx.doi.org/10.4141/cjps89-144.

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Danthonia spicata, poverty-oat grass, is a native North American perennial grass of pioneer habitats. It invades agricultural lands in eastern Canada with dry soil and low fertility. Unpalatable to livestock, it is an increaser species in heavily grazed or nutrient depleted pasture. A polymorphic reproductive system incorporates chasmogamy, cleistogamy and heteromorphic diaspores (dispersal unit). Clavicipitaceous fungal parasites are often present and affect productivity, reproduction, competitive fitness and possibly predation of their hosts.Key words: Danthonia spicata, Poverty oat grass, w

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34

Mukhiddinov, T. I., A. A. Abdullayev, E. Kuchkarov, A. H. Choriev, and S. K. Jumaev. "Inheritance of cleistogamy in interspecific hybridization of Gossypium barbadense L." Vavilov Journal of Genetics and Breeding 19, no. 1 (2015): 63. http://dx.doi.org/10.18699/vj15.007.

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35

Honda, Ichiro, Yerlan Turuspekov, Takao Komatsuda, and Yoshiaki Watanabe. "Morphological and physiological analysis of cleistogamy in barley (Hordeum vulgare)." Physiologia Plantarum 124, no. 4 (2005): 524–31. http://dx.doi.org/10.1111/j.1399-3054.2005.00541.x.

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36

Kubo, Katashi, Naoyuki Kawada, Masaya Fujita, Koichi Hatta, Shunsuke Oda, and Takashi Nakajima. "Effect of cleistogamy on Fusarium head blight resistance in wheat." Breeding Science 60, no. 4 (2010): 405–11. http://dx.doi.org/10.1270/jsbbs.60.405.

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37

LU, YINGQING. "Why is cleistogamy a selected reproductive strategy in Impatiens capensis." Biological Journal of the Linnean Society 76, no. 3 (2002): 463. http://dx.doi.org/10.1046/j.1095-8312.2002.d01-7.x.

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38

Jacquemart, Anne-Laure, and Jacques R. De Sloover. "The Part Taken by Cleistogamy in Narthecium ossifragum Reproductive Strategy." Flora 187 (1992): 67–72. http://dx.doi.org/10.1016/s0367-2530(17)32215-6.

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39

Saxena, K. B., Laxman Singh, and R. P. Ariyanayagam. "Role of partial cleistogamy in maintaining genetic purity of pigeonpea." Euphytica 66, no. 3 (1993): 225–29. http://dx.doi.org/10.1007/bf00025307.

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40

Gradziel, Thomas M., and Steven A. Weinbaum. "High Relative Humidity Reduces Anther Dehiscence in Apricot, Peach, and Almond." HortScience 34, no. 2 (1999): 322–25. http://dx.doi.org/10.21273/hortsci.34.2.322.

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The regulation of anther dehiscence by relative humidity (RH) was assessed for detached anthers and detached whole flowers from a limited selection of apricot (Prunus armeniaca L.), peach [P. persica (L.) Batsch], and almond [P. dulcis (Mill.) D.A. Webb, syn. P. amygdalus Batsch; P. communis (L.) Arcangeli, non Huds.] genotypes, as well as an almond X peach F2 progeny. Dehiscence was evaluated at 33, 64, 87, 93 and 97% RH for detached anthers, and at 33, 64 and 97% RH for whole detached flowers. Anther dehiscence was suppressed with increasing RH for all genotypes. Apricot anthers showed the g

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41

Petit, Sophie, Annette T. Scanlon, Alivereti Naikatini, Tara Pukala, and Russell Schumann. "A novel bat pollination system involving obligate flower corolla removal has implications for global Dillenia conservation." PLOS ONE 17, no. 2 (2022): e0262985. http://dx.doi.org/10.1371/journal.pone.0262985.

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The Dilleniaceae is known to produce nectarless flowers pollinated by bees, but the fact that bats ingest Dillenia biflora pollen led us to question pollination assumptions for these trees. We aimed to identify the pollinators of D. biflora, check for nectar presence, and investigate potential for cleistogamy and global prevalence of this pollination system. We examined aspects of the pollination of D. biflora on two Fijian islands using video recordings, direct observations, hand pollination, measurements (flowers, bite marks, nectar), and monitoring. The flowers, receptive for one night, con

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42

Wang, Ning, Shunzong Ning, Jianzhong Wu, Akemi Tagiri, and Takao Komatsuda. "An Epiallele atcly1Affects the Expression of Floret Closing (Cleistogamy) in Barley." Genetics 199, no. 1 (2014): 95–104. http://dx.doi.org/10.1534/genetics.114.171652.

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43

Wang, Ning, Katsuyuki Kakeda, Masahiro Tomokazu, et al. "A novel mutant allele at the Cleistogamy 1 locus in barley." Theoretical and Applied Genetics 134, no. 10 (2021): 3183–93. http://dx.doi.org/10.1007/s00122-021-03884-1.

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44

LU, YINGQING. "Why is cleistogamy a selected reproductive strategy in Impatiens capensis (Balsaminaceae)?" Biological Journal of the Linnean Society 76, no. 3 (2002): 463. http://dx.doi.org/10.1111/j.1095-8312.2002.tb01705.x.

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45

Veena, V., and Santhosh Nampy. "Induced cleistogamy: A strategy for reproductive assurance in Murdannia nudiflora (Commelinaceae)." Botany 97, no. 10 (2019): 547–57. http://dx.doi.org/10.1139/cjb-2019-0007.

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Murdannia nudiflora (L.) Brenan is a day flower that is dependent on entomophilous pollination. Despite the lack of pollinator attractants and its short flower longevity, M. nudiflora shows high rates of fecundity, which lead to their rapid dispersal. In addition to monitoring the vegetative reproductive methods and the effect of select environmental parameters (atmospheric temperature, relative humidity, and precipitation rates) in M. nudiflora, we evaluated mating systems in this species via artificial crosses. This species has evolved to undergo autogamy to ensure reproductive success when

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46

LU, YINGQING. "Why is cleistogamy a selected reproductive strategy in Impatiens capensis (Balsaminaceae)?" Biological Journal of the Linnean Society 75, no. 4 (2002): 543–53. http://dx.doi.org/10.1046/j.1095-8312.2002.00039.x.

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47

Porras, R., and J. M. Mu�oz. "Cleistogamy inCentaurea melitensis (Asteraceae): Capitulum variability and spatio-temporal development patterns." Plant Systematics and Evolution 223, no. 3-4 (2000): 251–62. http://dx.doi.org/10.1007/bf00985283.

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48

Ueno, K., and H. Itoh. "Cleistogamy in wheat: genetic control and the effect of environmental conditions." Cereal Research Communications 25, no. 2 (1997): 185–89. http://dx.doi.org/10.1007/bf03543455.

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49

Yoshida, Hitoshi, Jun-Ichi Itoh, Shinnosuke Ohmori, et al. "superwoman1-cleistogamy, a hopeful allele for gene containment in GM rice." Plant Biotechnology Journal 5, no. 6 (2007): 835–46. http://dx.doi.org/10.1111/j.1467-7652.2007.00291.x.

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50

Calviño, A., and L. Galetto. "Cleistogamy in the rare high Andean perennial herb Cryptantha capituliflora (Boraginaceae)." Plant Systematics and Evolution 237, no. 1-2 (2003): 41–50. http://dx.doi.org/10.1007/s00606-002-0245-6.

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