Inhibition of flower development in Chenopodium rubrum by a photosynthetic inhibitor

1971 ◽  
Vol 49 (12) ◽  
pp. 2233-2237 ◽  
Author(s):  
Ramma Sawhney ◽  
Bruce G. Cumming

Cumming 1969 has demonstrated that the short-day plant Chenopodium rubrum (60°47′ N) is induced to flower if inductive darkness is substituted by a relatively long exposure to a low intensity light of a low red/far-red ratio (light emitted by BCJ lamps). DCMU (3(3,4-dichlorophenyl)-1,1-dimethyl urea), a photosynthetic inhibitor, inhibited flowering if applied during this inductive BCJ light period.Our experiments show that ascorbic acid and dichlorophenol-indophenol (which have been used as reducing agents in photosynthesis by various workers) overcome the effect of DCMU on flowering. Sugars are also effective in overcoming the DCMU effect. This indicates that DCMU acts specifically on photosynthesis and that there are no side effects.In Cumming's experiments DCMU was supplied at the start of a BCJ inductive period and then washed off at the end of the BCJ period. However, there are indications that DCMU may persist in the plant for several days after the medium on which plants are growing has been thoroughly washed off. This raises the question whether the action of DCMU is on induction in BCJ light or on subsequent development in white light. By applying DCMU during the BCJ period and terminating its effect by ascorbic acid + dichlorophenol-indophenol or sugars at the time of transferring to white light, no inhibition of flowering was found. This suggests that inhibition of photosynthesis during the inductive BCJ light had no detrimental effect on flowering. The inhibition of flowering by DCMU might be a result of inadequate photosynthesis in white light for development of floral primordia.

2015 ◽  
Vol 41 (5) ◽  
pp. 1035-1041 ◽  
Author(s):  
Hee-jae Kim ◽  
Wook Song ◽  
Eun Hee Jin ◽  
Jongkyu Kim ◽  
Yoonseok Chun ◽  
...  

1955 ◽  
Vol 33 (3) ◽  
pp. 251-258 ◽  
Author(s):  
Hugh P. Bell ◽  
Jane Burchill

In the lowbush blueberry, floret primordia appear during June. Floral parts appear in acropetal succession during July. Ontogenetically the carpels are at first appendicular and later receptacular. The epigynous floret, in miniature, is formed by the first of August. During this month, some reproductive tissue is differentiated in both ovary and stamens. The characteristic resting stage is assumed during the autumn. Mitosis was observed in material collected during January and by late winter a number of ovules had two adjacent archesporial cells, the outer one later becoming functional. Definite differentiation starts during March. Active growth, including the initiation of meiosis, becomes general during April. Meiosis is completed in the anthers during the first week of May and about a week later in the ovules. Subsequent development in the ovule is of the Polygonum type. The flower is mature by the last week in May.


2014 ◽  
Vol 71 (1) ◽  
pp. 23-27 ◽  
Author(s):  
Halina Kulikowska-Gulewska ◽  
Jan Kopcewicz

The seedlings of <em>Pharbitis nil</em>, a sesitive short-day plant (SDP), were cultivated under special photoperiodic conditions: 72-h-long darkness, 24-h-long white light with low intensity, 24-h-long inductive night. During 24-h-long inductive darkness the total content of gibberellins in cotyledons underwent fluctuations with a maximum at 0 h and 8 h, and a decrease at the end of the dark period. FR light applied at the end of the 24-h-long white-light period inhibited flowering. R light flash and partially exogenous GA3 added on cotyledons could reverse the effect of FR. The seedling growth was not affected by FR and R light irradiation, but was promoted by exogenous GA3 application. The obtained results suggest that gibberellins are involved in photoperiodic control of SDP <em>P. nil</em> flowering. This involvement has nothing in common with participation of gibberellins in the control of the elongation growth of seedlings.


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