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Relevant bibliographies by topics / Anther dehiscence

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Academic literature on the topic 'Anther dehiscence'

Author: Grafiati

Published: 4 June 2021

Last updated: 3 February 2022

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Journal articles on the topic "Anther dehiscence"

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Li, Qian, Ze Wu, Huijun Wu, Weimin Fang, Fadi Chen, and Nianjun Teng. "Transcriptome Profiling Unravels a Vital Role of Pectin and Pectinase in Anther Dehiscence in Chrysanthemum." International Journal of Molecular Sciences 20, no. 23 (2019): 5865. http://dx.doi.org/10.3390/ijms20235865.

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Chrysanthemum (Chrysanthemum morifolium (Ramat.) Kitamura) plants have great ornamental value, but their flowers can also be a source of pollen contamination. Previously, morphological and cytological studies have shown that anthers of some chrysanthemum cultivars such as ‘Qx-115′ fail to dehisce, although the underlying mechanism is largely unknown. In this study, we investigated the molecular basis of anther indehiscence in chrysanthemum via transcriptome analysis of a dehiscent cultivar (‘Qx-097′) and an indehiscent cultivar (‘Qx-115′). We also measured related physiological indicators duri

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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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LOMBARDI, JULIO ANTONIO. "A new species of Peritassa (Celastraceae) from Espírito Santo, Brazil." Phytotaxa 491, no. 1 (2021): 79–84. http://dx.doi.org/10.11646/phytotaxa.491.1.9.

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Peritassa formidolosa, the new species here described, differs from other species of Peritassa Miers by its unique combination of characters: anthers dehiscent by longitudinal slits, inconspicuous connectives, and campanuliform flowers. This new taxon is included into Peritassa because of these characteristics: anther dehiscence mode and short-tubular disc free from the ovary wall.

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Zhang, Hong, Zhiyong Zhou, and Jiandong An. "Pollen Release Dynamics and Daily Patterns of Pollen-Collecting Activity of Honeybee Apis mellifera and Bumblebee Bombus lantschouensis in Solar Greenhouse." Insects 10, no. 7 (2019): 216. http://dx.doi.org/10.3390/insects10070216.

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Pollen is important not only for pollination and fertilization of plants, but also for colony development of bee pollinators. Anther dehiscence determines the available pollen that can be collected by foragers. In China, honeybees and bumblebees are widely used as pollinators in solar greenhouse agriculture. To better understand the effect of solar greenhouse microclimates on pollen release and pollen-foraging behaviour, we observed the anther dehiscence dynamics and daily pollen-collecting activity of Apis mellifera and Bombus lantschouensis during peach anthesis in a solar greenhouse in Beij

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ÇETİNBAŞ, Aslihan, and Meral ÜNAL. "Anther Ontogeny and Microsporogenesis in Helianthus annuus L. (Compositae)." Notulae Scientia Biologicae 7, no. 1 (2015): 52–56. http://dx.doi.org/10.15835/nsb719474.

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In this study, anther ontogeny and microsporogenesis were analysed in Helianthus annuus L. The undifferentiated anther is ovoid-shaped and the differentiation starts with the appearance of archesporial cells. Mature anthers are tetrasporangiate. The anther wall is composed of epidermis, endothecium, middle layer and plasmodial tapetum. Endothecial cells show no fibrous thickening. Tapetum is amoeboid type with binucleate cells. Epidermal layer remains intact until anther dehiscence; however, middle layer, endothecium and tapetum disappear during development. At the end of regular meiotic divis

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Romero, María Florencia, Roberto Salas, and Ana Maria Gonzalez. "Pollen development and orbicule and pollen grain morphology in species of Cephalanthus (Rubiaceae-Naucleeae) from the Americas." Australian Journal of Botany 65, no. 3 (2017): 233. http://dx.doi.org/10.1071/bt16238.

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This paper is the first embryological report on the genus Cephalanthus L. and contributes to future studies in other genera of the tribe Naucleeae. The development of the anther wall in Cephalanthus glabratus (Spreng.) K. Schum. corresponds to the dicot type and microsporogenesis is simultaneous. The young wall of the anther has four layers; epidermis, endothecium, one middle layer and the secretory tapetum. The tissue of the septum has idioblasts with crystalline sand. In the wall of the mature anther, only the endothecium and remnants of epidermal cells were preserved. The occurrence and mor

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Weis, K. G., S. M. Southwick, and Michael E. Rupert. "Abnormal Anther and Pollen Development in Sweet Cherry Cultivars Resulting from Lack of Winter Chilling." HortScience 31, no. 4 (1996): 684d—684. http://dx.doi.org/10.21273/hortsci.31.4.684d.

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Lack of pollen dispersal was noted in various sites and cultivars of sweet cherry (Prunus avium) following one of California's warmest recorded winters (≈550 hours @ 7°C in the Central Valley). `Bing' cherry is thought to require 850 to 880 hours for adequate budbreak and bloom development. Cross pollination is required by most sweet cherry cultivars for fruit set, including `Bing'. Complete anther dehiscence averaged 13% in `Bing' trees sampled, compared to 52% in `Rainier', 65% in `Brooks', 84.5% in `Burlat', 33% in Van, 23% in `Larian', and 86% in `Black Tartarian'. A range of degree of deh

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Hausbrandt, L., and W. Golinowski. "Rozwój warstw ściennych i otwieranie się pylnika u kilku dzikich gatunków ziemniaka (Solarium chacoense Bitt., S. phureja Juz. et Buk., 5. giberulosum Juz. et Buk., S. Commersonii Dun.) [The development of the parietal layers and dehiscence of the anthers at some wild potato species (Solanum chacoense Bitt., S. phureja Juz. et Buk., S. giberulosum Juz. et Buk., and S. Commersonii Dun.]." Acta Agrobotanica 28, no. 1 (2015): 89–93. http://dx.doi.org/10.5586/aa.1975.007.

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The anthers in these species like in whole genus <i>Solanum</i> are poricidal still some differences have been observed in structure of their anther walls. The fibrous cells associated with dehiscence restricted usually to the area around the pore may form a single layer or may form compact mass often irregular in thickness or it may be lacking at all. Besides the apical pore one can observe a lateral dehiscence. By desintegra-tion of cells a gap is forming in the wall separating the two anther chambers which causes breaking it down. Then stomium like cells in epidermis contribute

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Xiao, Yanjia, Shimin You, Weiyi Kong, et al. "A GARP transcription factor anther dehiscence defected 1 (OsADD1) regulates rice anther dehiscence." Plant Molecular Biology 101, no. 4-5 (2019): 403–14. http://dx.doi.org/10.1007/s11103-019-00911-0.

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Zheng, Lanjie, Punita Nagpal, Gonzalo Villarino, et al. "miR167 limits anther growth to potentiate anther dehiscence." Development 146, no. 14 (2019): dev174375. http://dx.doi.org/10.1242/dev.174375.

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Dissertations / Theses on the topic "Anther dehiscence"

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Dennis, Ruth. "Analysis of anther dehydration : a process required for anther dehiscence and pollen release." Thesis, University of Nottingham, 2018. http://eprints.nottingham.ac.uk/49599/.

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In flowering plants, the opening of the anther to release pollen is carefully timed to maximise reproductive potential. Manipulation of this process is an important tool for plant breeding and the production of hybrid crops. Dehydration of the anther epidermis, combined with the presence of secondary thickening within the endothecium layer, is required to create biomechanical changes that enable anther dehiscence. Both passive and active processes contribute to the targeted removal of water from the anther walls, however the genetic factors controlling water movement are not known. Furthermore

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Mo, Rui. "Characterising the regulatory network of MYB26 during anther dehiscence." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/39683/.

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Pollen development and release involves a number of important stages, which govern the success of fertilisation and thus indirectly crop yields. The secondary cell wall in the anther plays a pivotal role in anther dehiscence by offering mechanical strength required for opening and pollen release (Wilson et al. 2011). MYB26/MALE STERILE35(MS35) is a key regulator of the secondary thickening development in anther, mutation of this gene results in a failure of anther dehiscence and functional male sterility (Steiner-Lange et al. 2003; Yang et al. 2007). However, the regulatory network of MYB26 re

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Song, Jie. "MYB26 controls arabidopsis anther dehiscence by regulating secondary thickening in the endothecium." Thesis, University of Nottingham, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.523648.

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Sozen, Emel. "Characterisation of ms35, a critical gene for anther dehiscence in Arabidopsis thaliana." Thesis, University of Nottingham, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.323331.

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Makki, Rania. "Analysis of the role of MYB26-interactors and genes associated with anther dehiscence." Thesis, University of Nottingham, 2015. http://eprints.nottingham.ac.uk/29074/.

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Pollen development is critical for plant reproduction. Numerous nuclear mutations affect the function of pollen resulting in male sterility. The myb26 mutant is one such male sterile mutant allele, which results in anther indehiscence. Five putative MYB26 interactive proteins were previously identified from screening an Arabidopsis stamen yeast-2-hybrid library with MYB26 as bait. These proteins include Y2H128, Y2H320, Y2560, Y2H620 and Y2H970. Transient expression of these proteins, except Y2H128 were studied in planta by infiltration of Nicotiana benthamiana leaves and all were found to be e

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Trevizor, Ana Mayumi Hayashi. "Influência da área de reserva legal sobre a biologia da polinização de SOLANUM LYCOPERSICUM L. híbrido pizzadoro (SOLANACEAE)." Universidade Federal de São Carlos, 2014. https://repositorio.ufscar.br/handle/ufscar/27.

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Made available in DSpace on 2016-06-02T18:55:27Z (GMT). No. of bitstreams: 1 5930.pdf: 2008307 bytes, checksum: d0e45679fd9d345a26733ef3c1512046 (MD5) Previous issue date: 2014-03-28<br>Financiadora de Estudos e Projetos<br>It is estimated that approximately 73 % of the world crops are pollinated by a bees. The constant alteration of habitats has led to the decline of pollinators, which may reflect limitations in the quantity and quality of the fruits and seeds grown, becoming one of the biggest problems when it comes to agricultural production. Studies with agricultural crops and their poll

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Dai, Shu-Yu, and 戴書瑜. "The Gene ANTHER DEHISCENCE REPRESSOR Controls Anther Dehiscence by Suppressing the Jasmonate Biosynthetic Pathway and Anther Cell Wall Thickening in the Peroxisomes of Arabidopsis." Thesis, 2017. http://ndltd.ncl.edu.tw/handle/81045955506248531254.

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博士<br>國立中興大學<br>生物科技學研究所<br>105<br>Male-sterility in plants is caused by various stimuli such as hormone change, stress, cytoplasmic and nuclear mutations. Our previous study showed a gene Anther Dehiscence Repressor (ADR) which is modified by N-myristoylation may be involved in regulating male-sterility in Arabidopsis. 35S::ADR transgenic Arabidopsis showed male-sterility due to anther indehiscence. The male-sterility of 35S::ADR was rescued by the application of JA to the transgenic floral buds. Besides, genes participate in JA (jasmonic acid) biosynthesis were suppressed in 35S::ADR transge

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Wu, Pei-Jhen, and 吳佩眞. "The Reproductive Development, Anther Dehiscence and Pollen Viability of Yard-long Bean." Thesis, 2011. http://ndltd.ncl.edu.tw/handle/08596295965306953787.

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碩士<br>國立臺灣大學<br>園藝學研究所<br>99<br>Yard-long bean (Vigna unguiculata ssp.sesquipedalis (L.) Verdc.) thrives in warm weather with good tolerance to drought and to moisture. It has a wide range of soil adaptation and is an important summer vegetable in Taiwan. However, the crop succumbs to seed borne viral diseases and abrupt environmental changes often result in reduced pod yield and quality. Being a self-pollinated legume, yard-long bean usually has low seed set upon manual crossing. There is few report on the reproductive biology of the yard-long bean and it is essential to know the flowering an

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Yang, Hui-Ci, and 楊蕙慈. "Functional Analysis of CONSTANS-Like 9/10 in Regulating Anther Dehiscence in Angiosperms." Thesis, 2019. http://ndltd.ncl.edu.tw/cgi-bin/gs32/gsweb.cgi/login?o=dnclcdr&s=id=%22107NCHU5111025%22.&searchmode=basic.

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Yu, Yen-Ting, and 余晏霆. "Functional Analysis of CONSTANS-Like 9/10 in Regulating Anther Dehiscence in Plants." Thesis, 2016. http://ndltd.ncl.edu.tw/handle/84963872376904116088.

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碩士<br>國立中興大學<br>生物科技學研究所<br>104<br>CONSTANS (CO) is a transcriptional factor that belongs to CONSTANS-Like (COL) family and plays an important role in regulating vegetative-to-reproductive transition. COL family contains 17 different CO/COL proteins share one or two B-box domains at the N-terminus involved in protein-protein interaction, and a CCT domain at the C-terminus contained nuclear localization signals and a region highly conserved with HAP2 to interact with HAP3/5 for DNA binding and downstream genes regulation. We have previously shown that orchid’s COL9/10 functioned as activators,

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Book chapters on the topic "Anther dehiscence"

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Keijzer, C. J. "Mechanisms of Angiosperm anther dehiscence, a historical review." In Anther and Pollen. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-642-59985-9_6.

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