Effects of interpolated dark periods during the first long day of floral induction on the cell cycle in the shoot apex of Silene coelirosa

1987 ◽  
Vol 71 (3) ◽  
pp. 372-378 ◽  
Author(s):  
J. C. Ormrod ◽  
D. Francis
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.


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.


1996 ◽  
Vol 23 (5) ◽  
pp. 569 ◽  
Author(s):  
LT Evans ◽  
C Blundell

An acceleration of leaf primordium initiation by the shoot apex frequently follows floral evocation, but after varying intervals. The purpose of the experiments reported here was to define more closely the relation between this reduction of the plastochron and floral evocation, using the long day (LD) plant Lolium temulentum grown under closely controlled conditions.The acceleration begins at floral evocation, on the day after the first LD exposure, and increases after exposure to additional LDs. However, plants too young to be florally evoked by one LD nevertheless manifested an acceleration of primordium initiation, so the acceleration alone is not sufficient for evocation. Single applications of highly florigenic gibberellins (GAs), such as GA5, also accelerate the initiation of primordia and floral development, more so than does the weakly florigenic GA1. By contrast, single applications of the growth retardant Trinexapac-ethyl (CGA 163'935) to plants given one LD largely prevented the acceleration of primordium initiation but without inhibiting floral development. Thus, although the acceleration of primordium initiation by LD or by GA application is the first external sign of floral evocation in L. temulentum, it is neither a sufficient nor an essential component of it.


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