Effects of light on the cell cycle in the shoot apex ofSilene coeli-rosa L. on the first day of floral induction

PROTOPLASMA ◽  
1985 ◽  
Vol 124 (1-2) ◽  
pp. 96-105 ◽  
Author(s):  
J. C. Ormrod ◽  
D. Francis
PROTOPLASMA ◽  
1978 ◽  
Vol 96 (1-2) ◽  
pp. 81-88 ◽  
Author(s):  
D. Francis ◽  
R. F. Lyndon

1990 ◽  
Vol 17 (6) ◽  
pp. 629 ◽  
Author(s):  
KV Sharman ◽  
M Sedgley ◽  
D Aspinall

Flowering is inhibited in plants of Helipterum roseum grown under constant 25°C temperature conditions with a 12 h photoperiod and irradiance of 250 W m-2, but not at a constant temperature of 20°C. Floral inhibition was investigated by transferring plants between the two temperature con- ditions at different times to determine the morphological stage of inhibition, and by investigating cell-cycling at the shoot apex at the two temperatures. Floral initiation in Helipterum roseum was inhibited if the temperature increase from 20 to 25°C occurred at the doming of the apical meristem, and was delayed when the increase occurred at the initiation of involucral bracts. Steady-state cell-cycling was observed in the shoot meristem at 20°C and the cell-cycle duration was estimated at the morphological stages of large vegetative meristem, doming of the meristem and initiation of the involucral bracts. The length of the cell-cycle at these stages was 64 h, 41 h and 47 h respectively. Steady-state cell-cycling was not observed in shoot apical meristems at 25°C, and the meristem did not undergo the floral transition. It is concluded that the stage of commitment to flower is the initiation of involucral bracts, and that floral initiation is inhibited at 25°C by the loss of steady-state cell-cycling at the shoot apex.


1967 ◽  
Vol 45 (7) ◽  
pp. 955-959 ◽  
Author(s):  
Sidki Sadik ◽  
J. L. Ozbun

Cauliflower plants were induced to flower after being grown at 42 °F for varying periods of time, depending on the cultivar. Some of the histochemical changes in the shoot apex at the beginning of, during, and after floral induction were studied. During floral induction there is about a 20-fold increase in the volume of nucleoli and about a 3-fold increase in volume of nuclei. Apices of vegetative plants stained with bromophenol blue at pH 2.3, show small and dense nucleoli, dense and granular nuclei, and a small amount of weakly staining cytoplasm. In contrast, cells of apices of induced plants stained with bromophenol blue at pH 2.3, show large and dense nucleoli, large and weakly staining nuclei; however, these cells contain more and denser cytoplasm. Sections of vegetative and induced apices stained with alkaline fast green stained differently from those stained with bromophenol blue. Nucleoli did not stain and cytoplasm stained faintly with fast green while chromosomes stained strongly. Deoxyribonucleic acid (DNA) content of vegetative and induced apices are similar. Shoot apices of vegetative plants contained little or no starch. However, shoot apices of plants grown at 42 °F accumulate large amounts of starch. Floral primordia which develop into functional flowers are glutted with starch, while floral primordia which abort are void of starch.


1995 ◽  
Vol 7 (8) ◽  
pp. 1143 ◽  
Author(s):  
Hiroshi Kouchi ◽  
Masami Sekine ◽  
Shingo Hata

1967 ◽  
Vol 20 (1) ◽  
pp. 13 ◽  
Author(s):  
AHGC Rijven ◽  
LT Evans

Previous studies have shown an increase in RNA at the shoot apex of L. temulentum following floral induction, detectable chemically 2 days after induction, and by histochemical means after 1 day. Here, a transient increase in the incorporation of 32P, applied to leaves, into nucleic acids at the apex is shown to occur at about the time when the long-day stimulus is estimated to reach the shoot apex. The increased 32p incorporation due to the long-day exposure occurs throughout the apex, and is not confined to the summit region. Most of the 32p was incorporated into RNA.


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