SO2 Injury in Intact Leaves, as Detected by Chlorophyll Fluorescence

1988 ◽  
Vol 43 (3-4) ◽  
pp. 269-274 ◽  
Author(s):  
Wolfgang Schmidt ◽  
Ulrich Schreiber ◽  
Wolfgang Urbach
Keyword(s):  
Chlorophyll Fluorescence ◽  
Photosystem Ii ◽  
Calvin Cycle ◽  
Photosynthetic Apparatus ◽  
Enzymatic Reactions ◽  
Decay Kinetics ◽  
Saturation Pulse ◽  
Induction Kinetics ◽  
Fluorescence Measurements

The effects of short-time fumigation (0-60 min) of intact spinach leaves with SO2 (2 ppm) on the photosynthetic apparatus were investigated. A rather high SO2 concentration was applied to monitor immediate effects on the fluorescence behaviour with the influence of repair processes or secondary types of damage being minimized. Three different types of in vivo chlorophyll fluorescence measurements were used: Rapid induction kinetics (Kautsky effect), slow induction kinetics with repetitive application of saturation pulses (saturation pulse method), and decay kinetics following a single turnover saturating flash. The slow induction kinetics with repetitive application of saturation pulses reacts in the most sensitive way indicating a primary damage at the level of the enzymatic reactions of the Calvin cycle. It is suggested that stromal acidification upon SO2 uptake interferes with light activation of Calvin cycle enzymes. With longer fumigation times also damage at the level of photosystem II becomes apparent: A decrease in variable fluorescence yield reflects a lowering of photosystem II quantum yield, and the slowing down of fluorescence relaxation kinetics reveals an effect on the secondary electron transport from Qᴀ to Qв. The detrimental effects of SO2 depend to a great extent on the application of light during fumigation. Besides a light requirement for SO2 uptake by stomata opening also the possibility of photoinhibitory damage is discussed. The susceptibility of leaves to photoinhibition may increase with a lowering of Calvin cycle activity by SO2.

Humidity-sensitive Degreening and Regreening of Leaves of Borya nitida Labill. As Followed by Changes in Chlorophyll Fluorescence

1982 ◽  
Vol 9 (5) ◽  
pp. 587 ◽  
Author(s):  
SE Hethzerington ◽  
RM Smillie
Keyword(s):  
Chlorophyll Fluorescence ◽  
Relative Humidity ◽  
Photosystem Ii ◽  
Photosystem I ◽  
Fluorescence Induction ◽  
Physiological Age ◽  
Chlorophyll Fluorescence Induction ◽  
Induction Kinetics ◽  
Mediated Electron Transfer

Fast and slow chlorophyll fluorescence induction kinetics were used to follow changes in photosynthetic activity during humidity-sensitive degreening and regreening of leaves of Borya nidita Labill. During dry periods the leaves of this desiccation-tolerant plant lose chlorophyll, becoming yellow-brown and upon rehydration turn green again. This degreening process can be simulated in detached leaves by slow dehydration at 96% relative humidity. Under these conditions changes in chlorophyll fluorescence in vivo and the activities of photosystems I and II in chloroplasts isolated from dehydrated leaves indicated that degreening was accompanied initially by a stimulation of photosystem II activity and a gradual decrease in photosystem I-mediated electron transfer, while at advanced stages of degreening both photosystems were lost. Control leaves detached and kept at 100% relative humidity remained green and showed little change in chlorophyll fluorescence kinetics. During the rehydration and subsequent regreening of dry yellow leaves, photosystem I activity appeared to recover faster than photosystem II. The ability of the leaves to recover and regreen from the dried state, either on the plant or after detachment, depended upon the physiological age of the leaves at the time of dehydration.

Multiple Effects of Cadmium on the Photosynthetic Apparatus of Avicennia germinans L. as Probed by OJIP Chlorophyll Fluorescence Measurements

2007 ◽  
Vol 62 (3-4) ◽  
pp. 265-272 ◽  
Author(s):  
Daniel Gonzalez-Mendoza ◽  
Francisco Espadas y Gil ◽  
Jorge M. Santamaría ◽  
Omar Zapata-Perez
Keyword(s):  
Chlorophyll Fluorescence ◽  
Photosystem Ii ◽  
Water Splitting ◽  
Performance Index ◽  
Photosynthetic Apparatus ◽  
Reaction Centers ◽  
Avicennia Germinans ◽  
Fluorescence Measurements ◽  
Active Reaction ◽  
Primary Photochemistry

Abstract The toxic effects of cadmium on the photosynthetic apparatus of Avicennia germinans were evaluated by means of the chlorophyll fluorescence transient O-J-I-P. The chlorophyll fluorescence transients were recorded in vivo with high time resolution and analyzed according to the OJIP-test that can quantify the performance of photosystem II. Cadmium-treated plants showed a decrease in yield for primary photochemistry, TR0/ABS. The performance index of photosystem II (PSII), PIABS, decreased due to cadmium treatment. This performance index is the combination of the indexes of three independent parameters: (1) total number of active reaction centers per absorption (RC/ABS), (2) yield of primary photochemistry (TR0/ABS), and (3) efficiency with which a trapped exciton can move an electron into the electron transport chain (ET0/TR0). Additionally, the F0/Fv registered the highest sensitivity to the metal, thus indicating that the water-splitting apparatus of the oxidizing side of PSII is the primary site of action of cadmium. In summary, cadmium affects several targets of photosystem II. More specifically the main targets of cadmium, according to the OJIPtest, can be listed as a decrease in the number of active reaction centers and damage to the activity of the water-splitting complex.

Simultaneous Gas-Exchange and Fluorescence Measurements with Ozone-Fumigated Spruce

1994 ◽  
Vol 49 (11-12) ◽  
pp. 819-833
Author(s):  
Stefan Drenkard ◽  
Jürgen Maguhn ◽  
Dietmar Knoppik
Keyword(s):  
Gas Exchange ◽  
Calvin Cycle ◽  
Photosynthetic Apparatus ◽  
Early Summer ◽  
Assimilation Rate ◽  
Light Reaction ◽  
Fluorescence Measurements ◽  
Transport Chain ◽  
Short Time ◽  
Supply Information

A method was developed for carrying out gas-exchange and chlorophyll-fluorescence measurements simultaneously during fumigation of spruce twigs with peroxidic photooxidants. It is thus now possible to investigate how a pollutant affects distinct sectors of the photosynthetic apparatus of the plant: whereas fluorescence reveals any changes in the primary light reaction, CO2 gas-exchange measurements supply information about the biochemical reactions of the Calvin cycle. Results of short-time fumigation with 750 ppb ozone are presented here. Gas-exchange and fluorescence data are affected strongly in early summer, but not in autumn. The assimilation rate decreases significantly: primarily as a result of Rubisco activity and possibly because of direct inhibition of the electron-transport chain as well. Closure of the stomata leads to further reduction in the assimilation rate. Though no damage becomes visible on the needles, the perturbance of the photosynthetic apparatus caused by ozone fumigation is not reversible within 24 h.

scholarly journals Two Quenchers Formed During Photodamage of Phostosystem II and The Role of One Quencher in Preemptive Photoprotection

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Alonso Zavafer ◽  
Ievgeniia Iermak ◽  
Mun Hon Cheah ◽  
Wah Soon Chow
Keyword(s):  
Chlorophyll Fluorescence ◽  
Photosystem Ii ◽  
Time Course ◽  
Physiological Role ◽  
Reaction Centre ◽  
Time Resolved ◽  
Fluorescence Quencher

AbstractThe quenching of chlorophyll fluorescence caused by photodamage of Photosystem II (qI) is a well recognized phenomenon, where the nature and physiological role of which are still debatable. Paradoxically, photodamage to the reaction centre of Photosystem II is supposed to be alleviated by excitation quenching mechanisms which manifest as fluorescence quenchers. Here we investigated the time course of PSII photodamage in vivo and in vitro and that of picosecond time-resolved chlorophyll fluorescence (quencher formation). Two long-lived fluorescence quenching processes during photodamage were observed and were formed at different speeds. The slow-developing quenching process exhibited a time course similar to that of the accumulation of photodamaged PSII, while the fast-developing process took place faster than the light-induced PSII damage. We attribute the slow process to the accumulation of photodamaged PSII and the fast process to an independent quenching mechanism that precedes PSII photodamage and that alleviates the inactivation of the PSII reaction centre.

scholarly journals In vivo label-free mapping of the effect of a photosystem II inhibiting herbicide in plants using chlorophyll fluorescence lifetime

Plant Methods ◽  
2017 ◽  
Vol 13 (1) ◽  
Author(s):  
Elizabeth Noble ◽  
Sunil Kumar ◽  
Frederik G. Görlitz ◽  
Chris Stain ◽  
Chris Dunsby ◽  
...  
Keyword(s):  
Chlorophyll Fluorescence ◽  
Photosystem Ii ◽  
Fluorescence Lifetime ◽  
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