Influence of Nitrogen Fertilization and Foliar Application of Plant Growth Retardants and Zinc on Quantitative and Qualitative Properties of Egyptian Cotton (Gossypium barbadenseL. Var. Giza 75)

1997 ◽  
Vol 45 (8) ◽  
pp. 3331-3336 ◽  
Author(s):  
Zakaria M. Sawan ◽  
Mahmoud ◽  
Osama A. Momtaz
2000 ◽  
Vol 18 (2) ◽  
pp. 59-62
Author(s):  
S.E. Burnett ◽  
G.J. Keever ◽  
J.R. Kessler ◽  
C.H. Gilliam

Abstract In one experiment conducted in 1998 and two in 1999, Coreopsis rosea ‘American Dream’, or pink coreopsis, were treated with four plant growth retardants (PGRs): B-Nine from 2500 to 7,500 ppm, Cutless from 25 to 150 ppm, Sumagic from 10 to 40 ppm, and Bonzi from 25 to 100 ppm. The study was conducted to determine whether PGRs could be used to suppress growth of pink coreopsis without delaying flowering or causing phytotoxicity. Application of B-Nine, Cutless, or Sumagic suppressed plant growth 13–31% at first flower and when plants were marketable (one-third of flowers open) in all experiments and improved plant quality compared to controls. Plants treated with B-Nine, Cutless, or Sumagic had quality ratings 52–67% higher than those of control plants when marketable; treated plants appeared denser and more floriferous. Time to first flower and to a marketable stage were minimally affected by PGR application, and no phytotoxicity was observed. Bonzi did not significantly control growth or affect flowering of pink coreopsis in any of the three experiments.


Forests ◽  
2020 ◽  
Vol 12 (1) ◽  
pp. 19
Author(s):  
Xiaodeng Shi ◽  
Siyu Chen ◽  
Zhongkui Jia

The effects of varieties, concentrations, and number of applications of plant growth retardants (PGRs) on the morphological, physiological, and endogenous hormones of Magnolia wufengensis L.Y. Ma et L. R. Wang were assessed to obtain the most suitable dwarfing protocol for M. wufengensis and to provide theoretical support and technical guidance for the cultivation and promotion of this species. One-year-old M. wufengensis ‘Jiaohong No. 2’ grafted seedlings served as the experimental materials. In the first part of the experiment, three PGRs (uniconazole, paclobutrazol, prohexadione calcium), three concentrations (500, 1000, 1500 ppm), and three applications (one, three, and five applications) were applied in dwarfing experiments to perform L9 (34) orthogonal tests. In the second part of the study, dwarfing experiments were supplemented with different high uniconazole concentrations (0, 1500, 2000, 2500 ppm). Spraying 1500 ppm uniconazole five times achieved the best M. wufengensis dwarfing effect, related indicators of M. wufengensis under this treatment were better than other treatment combinations. Here, M. wufengensis plant height, internode length, scion diameter, and node number were significantly reduced by 56.9%, 62.6%, 72.8%, and 74.4%, respectively, compared with the control group. This treatment increased superoxide dismutase (SOD) activity by 66.0%, peroxidase (POD) activity by 85.0%, soluble protein contents by 43.3%, and soluble sugar contents by 27.6%, and reduced malondialdehyde (MDA) contents by 32.1% in leaves of M. wufengensis compared with the control. The stress resistance of M. wufengensis was enhanced. The treatment also reduced gibberellin (GA3) levels by 73.0%, auxin (IAA) by 58.0%, and zeatin (ZT) by 70.6%, and increased (abscisic acid) ABA by 98.1% in the leaves of M. wufengensis. The uniconazole supplementation experiment also showed that 1500 ppm was the optimal uniconazole concentration. The leaves exhibited abnormalities such as crinkling or adhesion when 2000 or 2500 ppm was applied. Given the importance of morphological indicators and dwarfing for the ornamental value of M. wufengensis, the optimal dwarfing treatment for M. wufengensis was spraying 1500 ppm uniconazole five times.


1970 ◽  
Vol 23 (5) ◽  
pp. 1115 ◽  
Author(s):  
LG Paleg

Experiments with cell-free preparations of rat liver indicate that of the plant growth retardants Phosfon B, Phosfon D, B995, COlI, and Amo 1618 all but B995 inhibit at least one step between acetate and mevalonate in cholesterol biosynthesis. The results also demonstrate that all of the retardants, including B995, inhibit at least one step between mevalonate and cholesterol, and that several of them act at different points along this part of the biosynthetic sequence.


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