scholarly journals Flower Bud Abortion Influences Clonal Growth and Sexual Dimorphism in the Understorey Dioecious Shrub Aucuba japonica (Cornaceae)

2002 ◽  
Vol 89 (6) ◽  
pp. 675-681 ◽  
Author(s):  
T. ABE
2021 ◽  
Vol 22 (8) ◽  
pp. 3932
Author(s):  
Jing Cao ◽  
Qijiang Jin ◽  
Jiaying Kuang ◽  
Yanjie Wang ◽  
Yingchun Xu

The lotus produces flower buds at each node, yet most of them are aborted because of unfavorable environmental changes and the mechanism remains unclear. In this work, we proposed a potential novel pathway for ABA-mediated flower timing control in the lotus, which was explored by combining molecular, genetic, transcriptomic, biochemical, and pharmacologic approaches. We found that the aborting flower buds experienced extensive programmed cell death (PCD). The hormonal changes between the normal and aborting flower buds were dominated by abscisic acid (ABA). Seedlings treated with increasing concentrations of ABA exhibited a differential alleviating effect on flower bud abortion, with a maximal response at 80 μM. Transcriptome analysis further confirmed the changes of ABA content and the occurrence of PCD, and indicated the importance of PCD-related SNF1-related protein kinase 1 (NnSnRK1). The NnSnRK1-silenced lotus seedlings showed stronger flowering ability, with their flower:leaf ratio increased by 40%. When seedlings were treated with ABA, the expression level and protein kinase activity of NnSnRK1 significantly decreased. The phenotype of NnSnRK1-silenced seedlings could also be enhanced by ABA treatment and reversed by tungstate treatment. These results suggested that the decline of ABA content in lotus flower buds released its repression of NnSnRK1, which then initiated flower bud abortion.


1995 ◽  
pp. 185-192 ◽  
Author(s):  
B.H. Nakasu ◽  
F.G. Herter ◽  
D.L. Leite ◽  
M.C.B. Raseira

1978 ◽  
Vol 26 (1) ◽  
pp. 119-127
Author(s):  
D.P. de Vries ◽  
L. Smeets

As a basis for breeding cvs adapted to flowering in winter light conditions, the growth of hybrid tea rose seedlings under controlled conditions was studied. Irradiance varied from 4-24 W/m2, day length was 8 h, temperature 21 deg C. Like cvs, the seedlings sometimes aborted the flower bud at low light intensity. With increasing irradiances, the following phenomena were observed: the juvenile period of the seedlings shortened; plants were longer at bud formation, at first flowering and at flower bud abortion; leaf area and the number of petals increased. Leaf number was constant at all irradiances. Flowering seedlings were smaller at bud formation, but taller at actual flowering than blind ones. Blind seedlings had fewer leaves with a smaller area. (Abstract retrieved from CAB Abstracts by CABI’s permission)


2014 ◽  
Vol 94 (7) ◽  
pp. 1181-1193 ◽  
Author(s):  
Shunli Wang ◽  
Jingqi Xue ◽  
Noorollah Ahmadi ◽  
Patricia Holloway ◽  
Fuyong Zhu ◽  
...  

Wang, S., Xue, J., Ahmadi, N., Holloway, P., Zhu, F., Ren, X. and Zhang, X. 2014. Molecular characterization and expression patterns of PsSVP genes reveal distinct roles in flower bud abortion and flowering in tree peony (Paeonia suffruticosa). Can. J. Plant Sci. 94: 1181–1193. Container culture and flower forcing are used for off-season production of tree peony for the Chinese Spring Festival. Storage of potted tree peony for 10 d at 12°C in a refrigerator before 4°C chilling treatment can help new root growth and promote leaf development. Development from bud swelling to anthesis was divided into nine stages. Some aborted flower buds usually emerge in Stage III. Removal of two to four leaflets in an alternating pattern and applying gibberellic acid 3 (GA3) around the flower bud at Stage III can decrease the flower bud abortion rate and promote flower formation rate. Two MADS-box genes with homology to Arabidopsis SVP, designated PsSVP1 and PsSVP2, which probably caused flower-bud abortion, were isolated by reverse transcription-PCR. Sequence comparison analysis showed that PsSVP was most similar to SVP-like gene in apple. Phylogenetic analysis indicates that PsSVP was evolutionarily close to SVP-like genes from Malus domestica, SVP genes from Cruciferae and SVP-like genes from Vitis vinifera. The qRT-PCR results suggested that expression of PsSVP was high in vegetative growth phase, especially in the leaves of tree peony, and its expression was regulated by GA3. Further analysis showed that more PsSVP transcripted in the aborted flower bud, especially in the buds where leaflets grew well. It was deduced that PsSVP can promote vegetative growth and suppress flowering in tree peony. Thus, it is very important to further investigate PsSVP and decipher the mechanisms of flower-bud abortion to improve forcing culture of tree peony.


2007 ◽  
Vol 25 (2) ◽  
pp. 89-94 ◽  
Author(s):  
Genhua Niu ◽  
Denise S. Rodriguez ◽  
Yin-Tung Wang

Abstract A study was conducted to characterize the response of Gaillardia aristata Pursh to salinity (0.8, 2.0 or 4.0 dS/m) and growing media: 100% perlite (Perlite), 100% Sunshine Mix No. 4 (Mix), 1 to 1 (by vol) perlite and Sunshine Mix No. 4 (Perlite Mix), or 1 to 1 Sunshine Mix No. 4 and composted mulch (Mix Mulch). Type of medium did not influence shoot dry weight (DW). However, root to shoot DW ratio was highest for plants grown in Perlite. Shoot DW of plants irrigated with tap water (0.8 dS/m) was higher compared to those irrigated with saline solution at 2.0 or 4.0 dS/m, except for those grown in Mix. Salinity did not alter the root to shoot DW ratio. In general, elevated salinity led to relatively short plants. Plants were taller when grown in Perlite or Mix Mulch with fewer lateral shoots compared to plants grown in Mix and Perlite Mix. Flower bud abortion occurred in plants grown in Mix or Perlite Mix, while this phenomenon was not observed in plants grown in Perlite or Mix Mulch. Overall, plants performed better in Perlite and Mix Mulch than Mix and Perlite Mix.


2016 ◽  
Vol 371 (1706) ◽  
pp. 20150535 ◽  
Author(s):  
David Haig

Haploid gametophytes of bryophytes spread by clonal growth but mate locally, within an area defined by the range of sperm movement. Rarity of establishment from spores or vegetative competition can result in unisexual populations unable to reproduce sexually. Females typically outcompete males, probably because females expend fewer resources than males on the production of gametes. Extreme sexual dimorphism—tiny males growing as epiphytes on much larger females—has evolved many times. Haploid selfing is common in bryophytes with bisexual gametophytes, and results in completely homozygous sporophytes. Spores from these sporophytes recapitulate the genotype of their single haploid parent. This process can be considered analogous to ‘asexual’ reproduction with ‘sexual’ reproduction occurring after rare outcrossing between haploid parents. Ferns also produce bisexual haploid gametophytes but, unlike bryophytes, haploid outcrossing predominates over haploid selfing. This difference is probably related to clonal growth and vegetative competition occurring in the haploid but not the diploid phase in bryophytes, but the reverse in ferns. Ferns are thereby subject to stronger inbreeding depression than bryophytes. This article is part of the themed issue ‘Weird sex: the underappreciated diversity of sexual reproduction’.


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