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Journal articles on the topic 'Flowering'

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Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2024

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1

Kuitert, Arie Peterse, Wybe, and Arie Peterse. "Jananese flowering cherries." Journal of Forest Science 48, No. 7 (May 20, 2019): 328. http://dx.doi.org/10.17221/11892-jfs.

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The Japanese sato-zakura, literally “village cherries”, represent perhaps the most popular subject of dendrology and ornamental horticulture. The authors rose to the occasion to write an extraordinary account of Japanese cherries and shed more light on a still confused group of these aristocratic flowering trees. Kuitert teaches at the Kyoto University of Art and Design while Peterse is a dedicated plant breeder and researcher of the Japanese flowering cherries. Rarely do professors have the time, or take the time, needed to solely write such a thoroughly prepared text. Both Dutchmen paid attention to detail, and the result is a well-written, high-quality product.

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2

Boden, Scott A., David Weiss, John J. Ross, Noel W. Davies, Ben Trevaskis, Peter M. Chandler, and Steve M. Swain. "EARLY FLOWERING3 Regulates Flowering in Spring Barley by Mediating Gibberellin Production and FLOWERING LOCUS T Expression." Plant Cell 26, no. 4 (April 2014): 1557–69. http://dx.doi.org/10.1105/tpc.114.123794.

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3

Fukazawa, Jutarou, Yuki Ohashi, Ryuhei Takahashi, Kanako Nakai, and Yohsuke Takahashi. "DELLA degradation by gibberellin promotes flowering via GAF1-TPR-dependent repression of floral repressors in Arabidopsis." Plant Cell 33, no. 7 (April 3, 2021): 2258–72. http://dx.doi.org/10.1093/plcell/koab102.

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Abstract Flowering is the developmental transition from the vegetative to the reproductive phase. FLOWERING LOCUS T (FT), SUPPRESSOR OF OVEREXPRESSION OF CONSTANS1 (SOC1), and LEAFY (LFY) are floral integrators. These genes are repressed by several floral repressors including EARLY FLOWERING3 (ELF3), SHORT VEGETATIVE PHASE (SVP), TEMPRANILLO1 (TEM1), and TEM2. Although gibberellin (GA) promotes flowering by activating the floral integrator genes, the exact molecular mechanism remains unclear. DELLAs are negative regulators in GA signaling and act as coactivators of the transcription factor GAI ASSOCIATED FACTOR 1 (GAF1). GAs convert the GAF1 complex from a transcriptional activator to a repressor. Here, we show that GAF1 functions in the GA-dependent flowering pathway by regulating FT and SOC1 expression in Arabidopsis thaliana. We identified four flowering repressors, ELF3, SVP, TEM1, and TEM2, as GAF1-target genes. In response to GAs, GAF1 forms a transcriptional repressor complex and promotes the expression of FT and SOC1 through the repression of four flowering repressor genes, ELF3, SVP, TEM1, and TEM2.

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4

Giovannini, Annalisa. "Flowering." Journal of Crop Improvement 17, no. 1-2 (October 4, 2006): 227–44. http://dx.doi.org/10.1300/j411v17n01_08.

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5

Ng-A-Fook, Nicholas. "Flowering Horizons." Cultural and Pedagogical Inquiry 12, no. 2 (April 24, 2021): 119. http://dx.doi.org/10.18733/cpi29591.

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6

McFadden, Hugh, Fergus Allen, Micheal O'Siadhail, and Philip Casey. "Late Flowering." Books Ireland, no. 288 (2006): 225. http://dx.doi.org/10.2307/20632962.

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7

Hennig, L. "Flowering Highlights." Journal of Experimental Botany 65, no. 22 (June 30, 2014): 6479. http://dx.doi.org/10.1093/jxb/eru076.

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8

Bagnoli, Martina. "The Flowering." Art History 37, no. 3 (May 12, 2014): 566–69. http://dx.doi.org/10.1111/1467-8365.12088.

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9

P., R. "Flowering inferno." Nature 359, no. 6398 (October 1992): 776. http://dx.doi.org/10.1038/359776a0.

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10

Mitchell, Roger. "Flowering Snow." Organization & Environment 10, no. 3 (September 1997): 314–15. http://dx.doi.org/10.1177/0921810697103010.

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11

Meeks-Wagner, D. R. "Fast flowering." Trends in Plant Science 1, no. 3 (March 1996): 76–77. http://dx.doi.org/10.1016/s1360-1385(96)80037-9.

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12

Muers, Mary. "Flowering form." Nature Reviews Genetics 14, no. 7 (May 21, 2013): 442–43. http://dx.doi.org/10.1038/nrg3516.

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13

Casci, Tanita. "Flowering time!" Nature Reviews Genetics 3, no. 1 (January 2002): 8. http://dx.doi.org/10.1038/nrg714.

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14

Farrell, M. "Fine flowering." BMJ 299, no. 6706 (October 21, 1989): 1048. http://dx.doi.org/10.1136/bmj.299.6706.1048.

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15

Simpson, Gordon G. "NO flowering." BioEssays 27, no. 3 (2005): 239–41. http://dx.doi.org/10.1002/bies.20201.

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16

Amasino, Rick. "Editorial: Flowering." Seminars in Cell & Developmental Biology 7, no. 3 (June 1996): 379–80. http://dx.doi.org/10.1006/scdb.1996.0047.

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17

Murfet, Ian C., and James B. Reid. "Flowering in Pisum: Gibberellins and the Flowering Genes." Journal of Plant Physiology 127, no. 1-2 (March 1987): 23–29. http://dx.doi.org/10.1016/s0176-1617(87)80038-x.

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18

Zheng, Zifei, Penwei Chen, Shanshan Cao, Shiwei Zhong, Yiguang Wang, Liyuan Yang, Qiu Fang, Xiao Zheng, Hongbo Zhao, and Bin Dong. "EARLY FLOWERING3 Gene Confers Earlier Flowering and Enhancement of Salt Tolerance in Woody Plant Osmanthus fragrans." Forests 13, no. 11 (October 28, 2022): 1786. http://dx.doi.org/10.3390/f13111786.

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Osmanthus fragrans Lour. is popular in landscaping and gardening in Asia. In recent years, growing attention has been given to evergreen tree flowering and adaptation. EARLY FLOWERING3 (ELF3) plays an essential role in plant flowering regulation and abiotic stress tolerance. However, there is very little known about how the ELF3 gene affects flowering time and salt tolerance in O. fragrans. To elucidate the potential role of the flowering-related gene ELF3 in responding to salt tolerance, a significantly upregulated gene OfELF3 was obtained by RNA sequencing (RNA-seq) after salt treatment in O. fragrans. Our results showed that OfELF3 is a nuclear protein, which did not have a transcriptional activation ability. OfELF3 accumulation was determined in different tissues and the differentiation process of floral buds by qRT–PCR, and the gene was also significantly induced by salt stress treatment. In addition, overexpression of OfELF3 accelerated the flowering time of transgenic Arabidopsis lines, and an increase in the expression of flowering integrators such as AtFT, AtSOC1, and AtAP1 was investigated. Moreover, OfELF3 overexpression significantly improved the salt tolerance of transgenic plants, seed germination and root length of transgenic plants and was superior to those of the wild type (WT) under NaCl treatment at 4 days post-germination and the 5-day-old seedling stage, respectively. Similarly, phenotype and physiological indexes (REL, MDA and soluble protein) of 3-week-old transgenic plants were superior to the WT plants as well. Together, our results suggest that OfELF3 is not only a positive regulator in the regulation of flowering but is also involved in the salt tolerance response in O. fragrans.

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19

Arvind Kumar Goyal, Derhasat Narzary, Sushil Kumar Middha, and Talambedu Usha. "Incidence of synchronous sporadic flowering of four different species of bamboos in Kokrajhar District, BTAD, Assam, India." International Journal of Fundamental and Applied Sciences (IJFAS) 7, no. 1 (March 30, 2018): 10–12. http://dx.doi.org/10.59415/ijfas.v7i1.116.

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The successive generation continues in angiosperm through flowering. The parent plants of some of the members that belong to Poaceae family dies after flowering.A member of the subfamily Bambusoideae of Poaceae, bamboos, exhibit similar characteristics.In this paper, an attempt have been made to document the incidence of the flowering of bamboo in Kokrajhar district of BTAD, Assam.Four bamboo species viz. Bambusa assamica, Bambusa tulda, Dendrocalamus hamiltonii and Melocanna baccifera belonging to three different genera were recorded to flower sporadically during March-May 2015 at Chandrapara, Odlaguri, Baukhungri hills, Chandrapara respectively.All the recorded species were semelparous i.e. the life cycle of the plant ends with flowering. Thus if the flowering continues in the same frequency the time may come in near future when this invaluable natural resource might become endangered or even extinct. Thus, this is the need of the hour to apply biotechnological tools and develop protocols for propagation and conservation and thus, save this green gold from germplasm erosion

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20

Czinege, Anikó. "The setting of fenological- stadium of plum (Prunus domestica) varieties in 2012." Acta Agraria Debreceniensis, no. 51 (February 10, 2013): 93–96. http://dx.doi.org/10.34101/actaagrar/51/2069.

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We planted experimental trees, namely 6 plum varieties grafted on 6 plum rootstocks in the spring of 2010. Our aim was to observe differences in the fenological-stages of plum rootstock and variety combinations. ‘Cacanska lepotica’, ‘Jojo’, ‘Katinka’, ‘Topfive’, ‘Topper’, ‘Toptaste’ plum varieties were planted on ‘Mirobalan’ (Prunus ceresifera var. ceresifera cv. myrabolan); damson (Prunus institicia) – ‘St Julien A’, ‘St Julien GF655/2’; and ‘Wawit’; ‘Wangwnheim’; ‘Fereley’ rootstocks. We observed the bud burst, the flowering course: at the start of the flowering, during the main flowering, and at the end of flowerings and the ripening of the plum. Finally we observed the difference in leaves falling observed in the case of the different varieties and rootstock combinations. The bursting of buds started with ‘Cacanska lepotica’, in March 16 and finished with ‘Jojo’ / ‘Mirobalan’ combination, in March 22. The starting of flowering course was in March 29 with ‘Topper’ / ‘St Julien GF655/2’ combinations and the end of flowering course finished with ‘Toptaste’ varieties, in April 3–4. The start of ripening of the plum was with ‘Katinka’ / ‘St Julien A’ combinations, in July 17. and the end of ripening of the plum finished with ‘Topper’ variety. The start of leaves falling began with ‘Cacanska lepotica’, in Sept 5–8 depending on irrigation, and ‘Katinka’, ‘Jojo’ varieties finished, in November 28–29.

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21

Chou, M. L., and C. H. Yang. "Late-Flowering Genes Interact with Early-Flowering Genes to Regulate Flowering Time in Arabidopsis thaliana." Plant and Cell Physiology 40, no. 7 (January 1, 1999): 702–8. http://dx.doi.org/10.1093/oxfordjournals.pcp.a029596.

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22

Hofmann, Nancy R. "Epitranscriptomics and Flowering: mRNA Methylation/Demethylation Regulates Flowering Time." Plant Cell 29, no. 12 (December 2017): 2949–50. http://dx.doi.org/10.1105/tpc.17.00929.

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23

Araki, Takashi, Yasushi Kobayashi, Hidetaka Kaya, and Masaki Iwabuchi. "The flowering-time geneFT and regulation of flowering inArabidopsis." Journal of Plant Research 111, no. 2 (June 1998): 277–81. http://dx.doi.org/10.1007/bf02512184.

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24

Takeno, Kiyotoshi. "Stress-induced flowering: the third category of flowering response." Journal of Experimental Botany 67, no. 17 (July 5, 2016): 4925–34. http://dx.doi.org/10.1093/jxb/erw272.

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25

Putterill, Jo. "Flowering in time: genes controlling photoperiodic flowering in Arabidopsis." Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences 356, no. 1415 (November 29, 2001): 1761–67. http://dx.doi.org/10.1098/rstb.2001.0963.

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Successful sexual reproduction in plants relies upon the strict coordination of flowering time with favourable seasons of the year. One of the most important seasonal cues for the model plant Arabidopsis thaliana ( Arabidopsis ) is day length. Genes influencing flowering time in Arabidopsis have been isolated, some of which are involved in the perception and signalling of day length. This review discusses recent progress that has been made in understanding how Arabidopsis integrates environmental and internal signals to ensure a sharp transition to flowering and new insights on the role of the circadian clock in controlling the expression of genes that promote flowering in response to day length.

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26

Lazaro, Ana, Yanhao Zhou, Miriam Giesguth, Kashif Nawaz, Sara Bergonzi, Ales Pecinka, George Coupland, and Maria C. Albani. "PERPETUAL FLOWERING2 coordinates the vernalization response and perennial flowering in Arabis alpina." Journal of Experimental Botany 70, no. 3 (November 27, 2018): 949–61. http://dx.doi.org/10.1093/jxb/ery423.

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27

Lakmes, Abdulkarim, Abdullah Jhar, R. Varma Penmetsa, Wenbin Wei, Adrian C. Brennan, and Abdullah Kahriman. "The Quantitative Genetics of Flowering Traits in Wide Crosses of Chickpea." Agriculture 12, no. 4 (March 30, 2022): 486. http://dx.doi.org/10.3390/agriculture12040486.

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Chickpea (Cicer arietinum L.) is one of the most ımportant food legume crops in the world. Chickpea is valued for its nutritive seed composition, which is high in protein content and used increasingly as a substitute for animal protein. Days to fırst flowerıng is an important component of the adaptation and productivity of chickpea in rainfed environments characterized by terminal drought and heat stress. This study aimed to identify the inheritance pattern and identify quantitative trait loci (QTLs) for days to first flowering and flowering color in F2:4 generation nested association mapping (NAM) populations of chickpea obtained using wide crosses between Gokce as the cultivated variety and wild accessions of C. reticulatum and C. echinospermum. A total of ten populations of 113 to 191 individuals each were grown under field conditions near Sanliurfa, Turkey. Two populations were genotyped for 46 single nucleotide polymorphism (SNP) markers, enabling QTL analysis. Flowering time differed between families, with the frequency distributions indicating quantitative inheritance controlled by both genes of major and minor effects. Three significant QTLs for the flowering time were mapped in one mapping family. For flower color, chi-square tests showed that five populations accepted single-gene action, two populations accepted two-gene action, and three populations accepted neither model. Two significant QTLs at three genomic regions were identified across the two genotyped populations. Days to first flowering was positively correlated with flower color for two of the ten populations. The diversity of QTLs identified underscored the potential of crop wild relatives of chickpea as sources of novel alleles for chickpea breeding.

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28

Yeung, Edward C. "Flowering Plant Embryology." Crop Science 44, no. 6 (November 2004): 2284. http://dx.doi.org/10.2135/cropsci2004.2284.

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29

Healy, W., and D. Graper. "FLOWERING OF STEVIA." Acta Horticulturae, no. 252 (September 1989): 137–42. http://dx.doi.org/10.17660/actahortic.1989.252.17.

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30

Melzer, Rainer. "Flowering Newsletter 2022." Journal of Experimental Botany 73, no. 14 (August 11, 2022): 4605–7. http://dx.doi.org/10.1093/jxb/erac269.

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31

Clarke, Adrienne E., Elizabeth Dennis, and Joseph Mol. "Forefronts of Flowering." Plant Cell 4, no. 8 (August 1992): 867. http://dx.doi.org/10.2307/3869454.

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32

van der Krol, Alexander R., Alan Brunelle, Suguru Tsuchimoto, and Nam-Hai Chua. "Petunia Flowering Revisited." Plant Cell 4, no. 11 (November 1992): 1349. http://dx.doi.org/10.2307/3869505.

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33

Swasey, James E. "Japanese Flowering Cherries." HortTechnology 9, no. 4 (January 1999): 691. http://dx.doi.org/10.21273/horttech.9.4.691.

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34

Kondo, Hiroshi, and Kiyotoshi Takeno. "Flowering and Epigenetics." PLANT MORPHOLOGY 19and20, no. 1 (2008): 15–27. http://dx.doi.org/10.5685/plmorphol.19and20.15.

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35

Hammer, Steven. "Lithops Flowering Stones." Cactus and Succulent Journal 77, no. 4 (July 2005): 194–95. http://dx.doi.org/10.2985/0007-9367(2005)77[194:lfs]2.0.co;2.

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36

Wada, Kaede C., and Kiyotoshi Takeno. "Stress-induced flowering." Plant Signaling & Behavior 5, no. 8 (August 2010): 944–47. http://dx.doi.org/10.4161/psb.5.8.11826.

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37

Danilevskaya, Olga N., Xin Meng, Brian McGonigle, and Michael G. Muszynski. "Beyond flowering time." Plant Signaling & Behavior 6, no. 9 (September 2011): 1267–70. http://dx.doi.org/10.4161/psb.6.9.16423.

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38

Tooke, F., and N. H. Battey. "Temperate flowering phenology." Journal of Experimental Botany 61, no. 11 (June 1, 2010): 2853–62. http://dx.doi.org/10.1093/jxb/erq165.

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39

Scanes, C. G. "Flowering of Science." Poultry Science 87, no. 3 (March 2008): 397–98. http://dx.doi.org/10.3382/ps.2008/87-03-397.

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40

May, Thomas. "A Flowering Tree." Jung Journal 2, no. 1 (January 2008): 41–48. http://dx.doi.org/10.1525/jung.2008.2.1.41.

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41

Huxley, Anthony. "Flowering of art." Nature 325, no. 6100 (January 1987): 118. http://dx.doi.org/10.1038/325118b0.

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42

McCarthy, Kayla, and Seth J. Davis. "Rediscovering natural flowering." Nature Plants 4, no. 10 (September 24, 2018): 750–51. http://dx.doi.org/10.1038/s41477-018-0267-x.

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43

Bishop, C. L. "Control of Flowering." Genome Biology 4 (2003): spotlight—20030422–03. http://dx.doi.org/10.1186/gb-spotlight-20030422-03.

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44

Crease, Robert P. "A flowering success." Physics World 31, no. 4 (April 2018): 20. http://dx.doi.org/10.1088/2058-7058/31/4/25.

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45

Clarke, A. E., E. Dennis, and J. Mol. "Forefronts of Flowering." Plant Cell 4, no. 8 (August 1, 1992): 867–70. http://dx.doi.org/10.1105/tpc.4.8.867.

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46

Musselman, Lytton J. "Parasitic Flowering Plants." Economic Botany 41, no. 2 (April 1987): 215. http://dx.doi.org/10.1007/bf02858968.

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47

Soltis, Douglas E. "Flowers and Flowering." Trends in Ecology & Evolution 24, no. 3 (March 2009): 124–25. http://dx.doi.org/10.1016/j.tree.2008.10.010.

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48

Sundberg, Marshall D. "Flowering Plant Embryology." Journal of Environmental Quality 33, no. 6 (November 2004): 2386. http://dx.doi.org/10.2134/jeq2004.2386.

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49

Osborne, I. S. "PHYSICS: Flowering Lasers." Science 298, no. 5598 (November 22, 2002): 1517a—1517. http://dx.doi.org/10.1126/science.298.5598.1517a.

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50

Bowler, Chris. "Flowering or wilting?" EMBO reports 1, no. 1 (July 2000): 7–9. http://dx.doi.org/10.1093/embo-reports/kvd006.

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