Shoot Apex Sugars in Relation to Long-Day Induction of Flowering in Lolium temulentum L

1991 ◽  
Vol 18 (2) ◽  
pp. 121 ◽  
Author(s):  
RW King ◽  
LT Evans

Inflorescence initiation in Lolium temulentum is induced by a single long day with a photoperiod extension of 16 h under low photon flux density (12 μmol PAR m-2 s-1) from incandescent lamps. Under these conditions the content of sucrose, the predominant free sugar in the shoot apex, fluctuates diurnally in the same way as in short day apices. There was no evidence of a greater apical sucrose content at any time during the long day or in the following period of high irradiance when floral evocation occurs. Thereafter, however, the diurnal fluctuation in apical sucrose content became more pronounced. Increasing the sugar supply to the apex by raising the photon flux density during the daily light period did not lead to flowering of non-induced plants; nor did the high contents of apical sugars reached in apices cultured in vitro on 5% sucrose medium. By contrast, when apices were excised after receipt of the floral stimulus from long day leaves, increase in the sugar content enhanced inflorescence development in vitro, this response being most pronounced after the inflorescences were initiated. Thus, floral evocation in L. temulentum does not require an increase in the content of sucrose at the apex although inflorescence development is highly responsive to it. When photoperiodic extensions with incandescent or fluorescent lamps were compared for their effects on apical sugars and flowering response, there was no interaction between light quality and photon flux density. Thus the shoot apex response to the low irradiance, photoperiodic time-measurement processes of leaves is distinct from the apical response to sugar supply. In Lolium temulentum floral evocation is controlled by the photoperiodic processes, the response to which is amplified by high sugar supplies but not replaced as it is in Sinapis alba.

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.


2016 ◽  
Vol 07 (14) ◽  
pp. 2087-2105 ◽  
Author(s):  
Patricia L. Sáez ◽  
León A. Bravo ◽  
Manuel Sánchez-Olate ◽  
Paulina B. Bravo ◽  
Darcy G. Ríos

2021 ◽  
Vol 168 ◽  
pp. 113597
Author(s):  
Diene Xavier Araújo ◽  
Tainá Teixeira Rocha ◽  
Alexandre Alves de Carvalho ◽  
Suzan Kelly Vilela Bertolucci ◽  
Ana Paula Ribeiro Medeiros ◽  
...  

HortScience ◽  
1995 ◽  
Vol 30 (4) ◽  
pp. 873B-873
Author(s):  
Y. Zhang ◽  
D. Donnelly

In vitro bioassays for screening and selection of salinity (NaCl)-tolerant potato have primarily focused on nodal cuttings. However, the relative tolerance of the microtuberization stage to salinized medium may be more relevant. A two-step microtuberization protocol was used in which in vitro layering was followed by microtuber induction in salinized media. `Norland', `Russet Burbank', and `Superior' shoots were layered in liquid Murashige and Skoog (1962) basal salt medium with 20 g sucrose/liter and incubated for 4 weeks at 25C with 50 μmol–m–2·s–1 photosynthetic photon flux density and 16-h day/8-h night period. Medium was replaced with liquid medium containing 80 g sucrose/liter and NaCl at 0, 80, or 160 mM. Cultures were incubated for 4 weeks at 15C with 50 μmol–m–2–s–1 photosynthetic photon flux density and 8-h day/16-h night period. Relative salinity tolerance of cultivars differed during the microtuberization stage. Low salinity (80 mM) stimulated, but high salinity (160 mM) depressed, microtuber yields compared with controls.


2019 ◽  
Vol 140 (3) ◽  
pp. 523-537 ◽  
Author(s):  
Márcio Rosa ◽  
Aurélio Rubio Neto ◽  
Vinícius de Oliveira Marques ◽  
Fabiano Guimarães Silva ◽  
Elisvane Silva de Assis ◽  
...  

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