Chlorophyll fluorescence quenching by oxygen in plants

1981 ◽  
Vol 59 (2) ◽  
pp. 190-198 ◽  
Author(s):  
William Vidaver ◽  
Konrad Colbow ◽  
Gordon Hall ◽  
Silvia Wessel

Three distinct phases of chlorophyll a fluorescence quenching were observed in green plants by applying O2 pressures of up to 400 atm. These phases are interpreted as indications of three different mechanisms of O2 quenching. The most sensitive phase is dependent on intersystem electron transport. For dark-adapted bean leaves this fluorescence was quenched to half the initial yield with an O2 pressure of about 3 atm. The second mechanism was observed with 3-(3,4)dichlorophenyl)-1,1-dimethylurea (DCMU), namely the quenching of variable fluorescence in leaves, chloroplasts, and green algae cells. This effect of O2 is thought to be closely associated with the photochemical system II reaction centers. Half of the variable fluorescence was quenched with about 40 atm of O2. Finally, the antennae pigments are quenched, as observed by the effect of O2 on the O-level fluorescence yield, when all photochemical system II reaction center traps are presumably open. The O2 pressure required for half-quenching in this case was about 400 atm.The possibility that the quenching of fluorescence occurs with O2 concentrations low enough for endogenous O2 to have an effect on in vivo fluorescence was investigated. We suggest that O2 quenches by competing with photochemical system I for electrons derived from water splitting, and may thus function as a feedback regulator of photosynthesis.

1990 ◽  
Vol 45 (11-12) ◽  
pp. 1133-1141 ◽  
Author(s):  
Michel Havaux ◽  
Reto J. Strasser

Modulated 685-nm chlorophyll fluorescence was measured under steady-state conditions in pea leaves adapted to moderate actinic light. When the measurements were performed after a short exposure to heat (42 °C) in darkness, the maximal (Fm) and steady-state (Fs) fluorescence levels were dramatically and irreversibly quenched whereas the basic fluorescence Fo remained unchanged. Concomitantly , photo synthetic O2 evolution was irreversibly inhibited. Analysis of the fluorescence data suggested that the heat treatment affected primarily the PS II reaction center, with the main effect being presumably an increased thermal dissipation of the excita­tion energy transferred to the reaction centers. In contrast, when heat stress was imposed in the presence of light, the loss of variable fluorescence (Fm-Fo) was much less marked and was fully reversible. In addition , no inhibition of in vivo O2 : evolution was observed when the samples heated in the light were recooled at 25 °C. The results indicate that light acted as an efficient protector of PS II against heat injury.


2011 ◽  
Vol 225 (1) ◽  
pp. 65-71 ◽  
Author(s):  
W.F. Falco ◽  
E.R. Botero ◽  
E.A. Falcão ◽  
E.F. Santiago ◽  
V.S. Bagnato ◽  
...  

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