Gibberellic acid and the light inhibition of stem elongation

Planta ◽  
1967 ◽  
Vol 75 (4) ◽  
pp. 291-308 ◽  
Author(s):  
Daphne Vince
1973 ◽  
Vol 21 (4) ◽  
pp. 245-255
Author(s):  
S.J. Wellensiek

Several selected S. armeria lines differing in their reaction to GA3 were treated with GA3 at various concentrations under short-day (SD) or long-day conditions. With SD treatment one application of GA3 at high concentration (10 000 p.p.m. or greater) induced flower formation in certain lines. Stem elongation increased with GA3 concentration and with plant age and was much greater on flowering plants than on non-flowering ones. [For previous related work see HcA 41, 4400.]. (Abstract retrieved from CAB Abstracts by CABI’s permission)


1968 ◽  
Vol 21 (5) ◽  
pp. 883 ◽  
Author(s):  
O H Caso ◽  
NP Kefford

O. juncea plants were grown in a variety of controlled conditions to determine effects of temperature, photoperiod, and gibberellic acid treatment on stem elongation (bolting) and flowering.


1992 ◽  
Vol 100 (1) ◽  
pp. 267-271 ◽  
Author(s):  
E Liscum ◽  
J C Young ◽  
K L Poff ◽  
R P Hangarter

2017 ◽  
Vol 39 (10) ◽  
Author(s):  
Daniela Soares dos Santos ◽  
Poliana Cardoso-Gustavson ◽  
Catarina Carvalho Nievola

HortScience ◽  
2012 ◽  
Vol 47 (5) ◽  
pp. 637-642 ◽  
Author(s):  
Alexander D. Pavlista ◽  
Dipak K. Santra ◽  
James A. Schild ◽  
Gary W. Hergert

To lower seed yield loss from directly harvested common bean or dry bean, height of the lower pod-bearing nodes needs to be raised. The objective of this greenhouse study was to stimulate lower stem elongation by gibberellic acid (GA3) of dry bean cultivars. Seeds of cv. Matterhorn, erect indeterminate Type II, and cv. Poncho, prostate indeterminate Type III, were dipped in GA3 at 62.5 to 16,000 ppm and planted. After 14 d, the height of the unifoliate and first trifoliate nodes showed maximum stimulation of stem elongation by 1000 ppm GA3 for ‘Poncho’ and by 2000 ppm for ‘Matterhorn’. Application of 1 mL of GA3 at 0.031 to 2048 ppm to newly expanded unifoliate leaves showed cultivar differences. Whereas ‘Matterhorn’ was promoted at 64 ppm and reached a maximum height by 512 ppm GA3, ‘Poncho’ was promoted at 0.25 ppm and reached a maximum height by 8 ppm GA3. Flowering of ‘Matterhorn’ was unaffected by GA3; flowering of ‘Poncho’ was completely inhibited by 128 ppm. The sensitivity difference of cultivars was verified with other cultivars. Type I cultivars, which are all determinate, showed a full range of GA3 sensitivity. Dry bean cultivars may be regrouped based on the GA3 dose to which they respond. Individual response to GA3 rates of dry bean cultivars needs to be predetermined using a short-term, 2–3 weeks, greenhouse bioassay before field use of GA3.


HortScience ◽  
2003 ◽  
Vol 38 (1) ◽  
pp. 113-116 ◽  
Author(s):  
Z.G. Tan ◽  
Y.L. Qian

Turfgrasses grown under low light conditions generally exhibit increased shoot elongation. Gibberellic acids (GAs), GA1 in particular, promote stem elongation in grass species. GA20 is the immediate precursor of GA1. However, a direct quantitative measurement of GA1 and GA20 has not been reported for turfgrass under different light intensities. This study was conducted in a greenhouse to quantify the endogenous levels of GA1 and GA20 of `KenblueTimes', `Livingston', and `NuGlade' Kentucky bluegrass (Poa pratensis L.) under two light intensities with and without trinexapacethyl (TE) application. GA1 and GA20 content in leaf tissue were analyzed using gas chromatography-mass spectrometry with deuterium-labeled GA1 and GA20 as internal standards. Light reduction of 73% under greenhouse conditions increased GA1 by 44% to 47% and GA20 by 16% to 50%. `NuGlade' had a GA1 content 20% lower than that of `Kenblue', suggesting that the dwarf characteristics of `NuGlade' may be related to its low GA1 content. The application of TE (0.1 kg·ha-1) reduced GA1 concentration by 47%, but increased GA20 concentration by 146%, supporting the contention that TE inhibited GA1 biosynthesis by blocking the conversion of GA20 to GA1. Chemical names used: 4-(cyclopropyl- -hydroxy-methylene)-3,5-dioxo-cyclohexanecarboxylic acid ethyl ester (trinexapac-ethyl); gibberellic acid (GA).


HortScience ◽  
1998 ◽  
Vol 33 (3) ◽  
pp. 494b-494
Author(s):  
J. P. Morales-Payan

Container experiments were conducted in the Dominican Republic to determine the effects of gibberellic acid applications on the `White', `Green', and `Spiny Green' tayota (Sechium edule) Dominican types. Young plants (25 cm in length) of the three types were sprayed with aqueous solutions of gibberellic acid at rates 0, 50, 100, 150, and 200 parts per million. A completely randomized design with seven replications was utilized. Plant height and shoot dry weight were determined 30 days after treatment and resulting data was subjected to analysis of variance and regression analysis. Gibberellic acid treatment significantly increased tayota shoot dry weight and stem elongation. Both variables responded with similar patterns to gibberellic acid application. A linear regression (Y = 39.82 + 0.214 X, r2 0.95) described stem elongation as a function of gibberellic acid rates. Results show that gibberellic acid can be effectively used in either tayota type to promote early stem elongation. From a practical standpoint, due to the climbing nature of Sechium edulis, rapid stem elongation could be instrumental in a more rapid establishment of the crop vines in the trellis system, as well as to provide the crop with an advantage on weeds competing for light during the usually critical early growth stages.


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