Simultaneous in vivo measurements of prompt fluorescence (PF), delayed fluorescence (DF) and 820-nm reflection (MR) were made to probe response of pea leaves to 40 s incubation at high temperatures (25–50°C). We interpret our observation to suggest that heat treatment provokes an inhibition of electron donation by the oxygen evolving complex. DF, in a time range from several microseconds to milliseconds, has been thought to reflect recombination, in the dark, between the reduced primary electron acceptor QA– and the oxidized donor (P680+) of photosystem II (PSII). The lower electron transport rate through PSII after 45 and 50°C incubation also changed DF induction. We observed a decrease in the amplitude of the DF curve and a change in its shape and in its decay. Acceleration of P700+ and PC+ re-reduction was induced by 45°C treatment but after 50°C its reduction was slower, indicating inhibition of photosystem I. We suggest that simultaneous PF, MR and DF might provide useful information on assessing the degree of plant tolerance to different environmental stresses.
Citation: Oukarroum A, Goltsev V, Strasser RJ (2013) Temperature Effects on Pea Plants Probed by Simultaneous Measurements of the Kinetics of Prompt Fluorescence, Delayed Fluorescence and Modulated 820 nm Reflection. PLoS ONE 8(3): e59433. https://doi.org/10.1371/journal.pone.0059433
Editor: Rajagopal Subramanyam, University of Hyderabad, India
Received: October 29, 2012; Accepted: February 14, 2013; Published: March 19, 2013
Copyright: © 2013 Oukarroum et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Abdallah Oukarroum and Reto J. Strasser acknowledge support by the Swiss National Science Foundation, Project No. 200021-116765; Vasilij Goltsev acknowledges the Bulgarian National Science Fund, Project No. DO 02-137/15.12.2008 for the financial support. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Simultaneous chlorophyll (Chl) a fluorescence and 820-nm transmission measurements have provided strong experimental evidence that the three phases (i.e. O-J, J-I and I-P) of the prompt fluorescence rise OJIP  reflect three different reduction processes of the electron transport chain , , . Following a dark-to-light transition of a photosynthetic sample, prompt fluorescence (PF) is emitted and during light-to-dark transition, delayed fluorescence emission (DF) is detected , . DF was discovered by Strehler and Arnold . It is mainly emitted from photosystem II (PS II), and photosystem I (PS I) contributes very little to the DF emission . PF depends on the redox state of the PS II reaction centers (RC); however the DF in a time range from several microseconds to milliseconds, after light excitation, has been thought to reflect the recombination, in the dark, between the reduced primary electron acceptor QA– and the oxidized donor (P680+) of PSII that are formed after light-induced charge separation . DF has components that decay in very different time domains. From microseconds to milliseconds, DF has been thought to reflect the recombination between the reduced electron acceptor QA– and the oxidized secondary electron donor, Z+, of PSII . In the second time range, DF is associated with the recombination of S2 and S3 states of the oxygen-evolving complex (OEC) with QA– and QB– –.
Among others, Grabolle and Dau  have reported that the emission spectra of the prompt chlorophyll fluorescence and delayed fluorescence emission in PII membrane particles of spinach are essentially identical. The intensity of DF depends directly on the rate of backward electron transport reactions in the RC of PSII , . The shape of the DF induction curve depends on the sample type and its physiological state , , ; further, DF induction curve depends on the kinetic components of DF being measured .
High temperature effects on PSII using PF have been measured by many authors –. It is known that the exposure of plants to high temperatures leads to a loss of the manganese cluster , , , which leads to changes in the structure and function of PSII , . The manganese cluster of PSII has been identified as the most heat sensitive component of the photosynthetic electron transport chain . One of the earliest events that take place due to heat stress is the loss of grana stacking following dissociation of peripheral light-harvesting complexes from the core complex , .
At elevated temperatures, changes in lipid–protein interactions have been associated with increased lipid fluidity of the thylakoid membranes  and a close relationship between the physical state of membrane lipids and delayed chlorophyll fluorescence intensity have been observed . In another study, lipid unsaturation was found to exert a strong effect on the delayed fluorescence . Simultaneous measurements of the kinetics of PF, and transmission at 820 nm changes at higher temperature have been used to monitor heat treatment (48°C) on electron flow through PSI in pea plants ; that in heat-treated samples the electrons responsible for P700+ and PC+ reduction arrived much more slowly than in the control samples.
In this study heat-stress-induced changes in PSII photochemistry of pea plants was obtained in vivo, using three signals- PF, DF and modulated 820 nm reflection (MR), measured simultaneously. We have shown that simultaneous measurement of PF, DF and MR is an important tool to characterize the effect of high temperature on intact photosynthetic systems and can be used as a tool to monitor these changes induced in the photosynthetic membranes.
Materials and Methods
Plants and Heat Treatment
Pea plants (Pisum sativum L. cv. Ambassador) were grown in the greenhouse with day/night air temperature of 25/18°C, under long-day conditions (16 h light, 8 h dark). The intensity of light used during growth of the plants was 120 µmol photons m−2 s−1; sometimes, additional light was given, if needed (OSRAM HQIT 400 W lamps were used). The plants were grown in plastic pots (4 l) containing commercial peat soil.
Two week grown pea plants were kept in dark for at least 1 h. Mature and detached leaves were used in this study. The leaves were submerged in water for 40 s at various temperatures (25, 30, 35, 40, 45 and 50°C) in the dark, and then the kinetics of prompt fluorescence, delayed fluorescence and modulated 820 nm reflection were measured simultaneously after 5 min relaxation at room temperature. Five different leaves were measured for each temperature.
The Multifunctional Plant Efficiency Analyser M-PEA
In the M-PEA instrument emitter wavelength ranges are: (1) 627±10 nm, for the actinic light LED; (2) 820±25 nm, for the modulated light LED, and (3) 735±15 nm, for the far-red light LED; the latter uses a RG9 long pass filter to remove any visible light component (see , , and Kalaji et al. 2012). High quality optical band pass filters were used for the protection of the detectors of prompt and delayed fluorescence (730±15 nm) and modulated reflection (820±20 nm). The LED emitting in the far-red (735±15 nm; 1000 µmol photons m−2 s−1 at 100%) was used when fast re-opening of PSII reaction centers was required (e.g., for samples being at the light-adapted state). The actinic light LED is built into the centre of the optical sensor unit and focused onto the sample surface to provide homogeneous illumination over the exposed circular area (2 mm diameter), with an intensity of 5000 µmol photons m−2 s−1 at 100%. The other emitters and detectors are built on the periphery of the unit. The data acquisition for the three signals, PF and MR in the light, and DF in the dark, is every 0.01 ms in the digitalization range 1 (0.01–0.3 ms), every 0.1 ms in range 2 (0.3–3 ms), every 1 ms in range 3 (3–30 ms), and then decreases until range 7 (30–300 s), where the data acquisition is every 10 s.
During one measure, the measuring cycle includes light and dark periods in the ratio of 3∶1. The duration of the cycle is increased during the induction in sequence: 400 µs, 4, 10, 100 ms, 1 and 10 s (a schematic representation of the timing protocol for simultaneous recording of prompt and delayed chlorophyll fluorescence was shown in ). During the cycle, the PF is measured when the actinic light is on and DF is recorded when the light is off.
The calculated ratio MR/MR0 (MR0 is the value at the onset of the actinic) is complementary of the fraction (Iabs/Iinc)820 nm of incident light flux (Iinc) that is absorbed (Iabs) by the sample (at 820 nm). A decrease in the amplitude of MR/MR0 is equivalent to an increase of (Iabs/Iinc)820 nm; the latter is associated with a decrease of (Iabs/Iinc)700 nm (photobleaching, at about 700 nm). A decrease of (Iabs/Iinc)700 nm corresponds to an increase in the concentration of oxidized states of PSI reaction center (P700+) and plastocyanin (PC+); accordingly, an MR/MR0 increase indicates P700+ and PC+ reduction .
Simultaneous Measurements of the Kinetics of Prompt Fluorescence, Delayed Fluorescence and Modulated 820 nm Reflection
Illumination of pea leaves exposed to 25°C exhibits a polyphasic PF rise. The fluorescence rise up to the J-step provides information about single turnover events of the primary reactions of photochemistry, mainly QA reduction . During the time interval from 2 to ∼200 ms, multiple charge separation occurs and the redox components of the electron transport chain become reduced (see  for review). The I–P phase is related to PSI activity , , . For modulated reflection signals the first reliable MR measurement was at 0.3 ms. The MR decrease exhibits photoinduced oxidation of P700 and accumulation of P700+ and PC+ until about 20 ms, this accumulation is in the range of the J–I phase of PF. Subsequently, the MR increase exhibits re-reduction of both P700+ and PC+ by the intersystem electrons in the range of the I–P phase of PF .
The DF induction curves, shown in Figure 1, are averaged DF values collected within different DF delay-time intervals during the dark period after interruptions of the actinic light (the analytical time within each dark interval, during which DF is recorded, was noted as delay-time). Energy level diagram for the PSII-states participating in DF generation has been presented by Grabolle and Dau  and Goltsev et al. . The calculated DF values are also presented against the JIP phase of PF . In the DF induction curve, two phases can be observed: the fast one until 200 ms includes the I1 and I2 peaks, and the slow one until several minutes , , . Further, included in our study is the I4 peak, according to nomenclature of Goltsev and Yordanov .
Measurements induced by a 10 s pulse of strong red actinic light (627 nm peak, 5000 µmol photons m−2 s−1) in pea leaves detached from the plants and dark-adapted for 1 h. PF, DF and MR measured simultaneously with M-PEA (see Materials and methods) and plotted on a logarithmic time scale from 20 µs to 10 s (JIP-time). DF vs. delay-time recorded during the dark interruptions of the actinic light (see Materials and methods). The time values present delay-time intervals at which corresponding DF quanta are collected.
The DF curve measured at 10–30 µs delay-time consists of a fast rise to a peak I1 (at 7 ms), a subsequent decrease through I2 (at about 100 ms), and I3, sometimes found at the end of the fast phase. The origin of I3 and the conditions under which it appears are still uncertain. In slow-decaying components, concomitant with the disappearance of the first two maxima (I1 and I2) in the induction curve, an appearance of the peak I3 was observed, and this is mainly due to the slow millisecond components of DF . I3 was measured at lower actinic light ∼1200 µmol photons m−2 s−1 ; it was not visible in our experiments at high actinic light (5000 µmol photons m−2 s−1). The I4 level was observed at 5 s and finally a plateau (between 0.5 and 10 s) was observed (Figure 1). Goltsev et al.  suggested that the I1 maximum is a result of the rise of the transmembrane electrical gradient and of the accumulation of RCs with semi-reduced QB (Z+P680QAQB−), while I2 was associated with the increase of Z+P680QA−QB− states during PQ pool reduction. Zaharieva et al.  reported that the I2 maximum was probably related to the prolonged reopening of PSII RCs by the electron transfer from the reduced QB to PQ before the reduction of the PQ pool. They suggest that the relative size of this maximum increases with the decrease of the size of the PSII antenna and when the measuring temperature is increased.
In Figure 1, I1 is between the J-step towards the I-step of the PF curve and in the oxidation phase of MR measurements and corresponds to the time of decrease of MR (7–10 ms). I2 appeared in the range of the I–P phase of the PF and the re-reduction phase of MR measurements. I4 appeared during the decline of the PF curve. The three latest DF induction curves (DF vs. JIP-time) the peaks I1 and I2 disappeared (Figure 1).
High temperature induced modifications of photosynthetic activity in detached pea leaves were measured with M-PEA after dark treatment for 1 h. Figure 1 shows the kinetics of three signals (PF, DF and MR) obtained by illuminating a leaf-sample with a 10 s pulse of strong red actinic light (627 nm peak, 5000 µmol photons m−2 s−1) after 40 s incubation at 25°C (control conditions). The induction curves of PF, DF (left vertical axis) and MR (right vertical axis) are plotted on a logarithmic time scale from 20 µs to 10 s.
Figure 2 shows the changes in the shape and intensity of PF and DF transients of pea leaves following 40 s of exposure to different temperatures (25–50°C). We did not observed any change in shape and intensity of the PF and DF curves when the incubation temperature was increased up to 40°C. However the high temperature effect becomes more prominent as the temperature is increased beyond 40°C. After incubation at 45 and 50°C, we observed a decrease in the amplitude of the DF curve and a change in its shape with disappearance of DF decay between the I1 and I2 peaks. After 50°C incubation, the amplitude of DF curves decreased more than after 45°C incubation, and a decline of I1 was observed at 3 ms. After 50°C incubation, the peaks at I1 and I2 of the DF curve, observed at 7 and 100 ms, disappeared but we saw another peak at 200 ms, which seems to be different from that of I4. In the PF curve, the K peak (0.3 ms) appeared clearly after treatment at 50°C and its appearance has been associated with the destruction of the oxygen-evolving-complex (OEC) by heat stress , .
Measurements induced by a 10 s pulse of strong red actinic light (627 nm peak, 5000 µmol photons m−2 s−1) in pea leaves detached from the plants dark-adapted for 1 h and heated to various temperatures (25, 30, 35, 40, 45 and 50°C) for 40 s in darkness.
Kinetics of Delayed Fluorescence
Figure 3 shows DF decay kinetics at I1, I2 and I4 (at 7 ms, 100 ms and 5 s, respectively); here, the DF decay kinetics is presented on a logarithmic time scale, from 0.01 to 0.9 ms (the common range for all three DF decay kinetics). For treatments from 25 to 40°C, the three decay kinetics were different in their average decay rates; this rate was largest for I1. However after 45°C incubation, the decay kinetics at I1 and I2 were the same but still highest compared to the decay kinetics at I4. At 50°C, a higher decrease in the two decay kinetics at I1 and I2 was observed, and I1, I2 and I4 had the same decay kinetics. At microsecond and sub-millisecond time ranges, the DF dark relaxation curve is a polyexponential function. Figure 4A shows a deconvolution of the data monitored in the time window of 10 to 900 µs; it was performed by a numerical fit to the formula , where L1, L2 and L3 are the amplitudes of the kinetic components and τ1 and τ2 are their lifetimes . Two components were found in DF decay measured at the beginning of the induction curve (I1) in non-treated samples. The fast component has the amplitude L1 of 573.8±8.2 and lifetime τ1 of 23.6±0.5 µs. It was followed by a middle, sub ms component, that was characterized by L2 = 86.0±1.9 and τ2 = 300.9±23.4 µs. The possible origin of the fast DF component is charge recombination in the PSII reaction center in state ZP680+QA– , . This DF is considered to be a leakage type luminescence decay; it is a result of separated charge stabilization by re-reduction of P680+ by Yz. The 35-µs kinetics of reduction was shown in PSII membrane particles , , but it seems that it is coupled with additional processes (most likely proton and/or hydrogen transfer) which changes the fluorescence quantum yield , . If we propose that all light emitting states (LES) (as well as their dark decay reactions) do not change during induction, we would expect to find that the temperature dependence of the amplitudes of DF components (and their characteristic times), measured at I1, I2 and I4, would be similar, i.e., the temperature dependence of L1(I1)∼L1(I2)∼L1(I4) and τ1 (I1)∼τ1 (I2)∼τ1 (I4). But the data presented in Figure 4B, C, D show that this is not the case. Although the temperature dependences for τ1 at times of I1, I2 and I4 are similar, for τ2 they are similar also at time of I1, I2 and I4 points and amplitudes of DF components measured at I4 point showed different temperature dependence as compare to points I1 and I2 (it showed higher termostability). This fact is valid for L2 and L3 parameters. It is possible that LESs that are responsible for DF emission are more thermostable after 5–10 s illumination than in the beginning of the induction curve as a result of thylakoid membrane energization or as a result of acidification of the lumenal space. The amplitudes of the fast DF component, measured at the three induction points (I1, I2 and I4), decreased after incubation at temperatures higher than 40°C (Figure 4B). Inhibition of DF was accompanied by slowing down of the DF decay.
I1, I2 and I4 (at 7, 100 and 5000 ms respectively), indicated by closed circles, open circles and gray circles, respectively.
(A) Deconvolution was performed by a numerical fit to the formula and the residual (triangle symbol). Amplitudes of the kinetic components (open symbols) L1 (B), L2 (C) and L3 (D). τ1 (B) and τ2 (C) (closed symbols) are their lifetimes. I1, I2 and I4 were presented respectively by circles, triangles and squares.
The sub-ms (120–200 µs) component  in the DF decay curve is suggested to be leakage type luminescence generated from the reaction centers in the state , and the deactivation of these states is a result of the forward reaction of re-oxidation of QA– by QB, which occurs with a rate constant of 2500–5000 s−1 . High temperature pre-treatment has minimal effect on the middle component at temperatures below 40°C (Figure 4C). The temperatures 45–50°C accelerated the DF decay (decrease of τ2) and activated the DF emission (increased L2). The slow DF component is expressed by a constant L3. It reflects a sum of sub-millisecond and millisecond DF components. They are results of electron transport from QA to QB and from reduced QB to the plastoquinone pool , . Similar to the fast component, the amplitude of the slow component also decreased at two higher temperatures (Figure 4D).
Relationship between Prompt and Delayed Fluorescence
Figure 5 shows DF10–30 µs/PF, and DF10–30 µs/V(t) vs. time, where DF10–30 µs is delayed fluorescence signal at 10–30 µs delay time, and PF represents prompt fluorescence (in arbitrary units) and V(t) is the relative prompt fluorescence ((Ft-Fo)/(FM-Fo)). DF/PF expresses the rate of repopulation of excited Chl per absorption . We observe that the shape of (DF10–30 µs/PF) curve is different than that of DF10–30 µs curve (see Figure 2). The response to different temperatures after 5 min relaxation at room temperature is practically similar for heated leaves at 25, 30, 35 and 40°C treatment. However I1 peak shifts from 7 ms at 25°C to 10 ms and 30 ms respectively after 45 and 50°C treatment. The same observation was made for DF10–30 µs/V(t) vs. JIP-time curve, and, in addition, the amplitude of DF after 50°C treatment was found to be strongly higher.
(Vt = (Ft–Fo)/(FM−Fo)) measured at 20 µs after the interruption of the actinic illumination in pea leaves detached from the plants dark-adapted for 1 h and heated to various temperatures (25, 30, 35, 40, 45 and 50°C) for 40 s in darkness. Vt is the relative variable fluorescence.
In Figure 6 A, the I1, I2 and I4 peaks, obtained from DF10–30 µs curves, were plotted vs. temperature treatment. We observed that, upon temperature increase to 40°C, the DF10–30 µs curves decreased in amplitude for I1 and increased for I2 and I4. And at 50°C the I2 amplitude decreased. The changes in the amplitude in I1/I4, I2/I1 ratio and the K step, expressed as FK/FJ ratio, after different temperature treatment, are shown in Figure 6B. An increase of FK/FJ and I2/I1 ratios was observed and had similar results. On the other hand the I1/I4 ratio decreased significantly after the incubation temperature was increased. We observe that in the DF/PF curve the shoulders I2 and I4 increase but are more pronounced in I2 (Figure 6C). When we compare these data with FK/FJ, a positive linear correlation with the I2/I1 ratio is observed (r2 = 0.98) and this correlation is exponential with the I1/I4 ratio (r2 = 0.98) (Figure 6D).
(A) I1, I2 and I3 peaks were plotted vs. temperature treatment. B. Change of I1, I2 and I3 peaks obtained from DF10–30 µs normalized to the corresponding value obtained from PF vs. temperature treatment. (C) Changes in I1/I4, I2/I1 ratios and the amplitude of the K step, expressed as FK/FJ ratio to different temperature. (D) Correlation between FK/FJ and I2/I1 and I1/I4 parameters. The results are shown as the mean with standard deviations.
Modulated Reflection at 820 nm
Figure 7A show the kinetics of the normalized modulated reflection at 820 nm (MR) induced by red actinic light of 5000 µmol photons m−2 s −1 in heated leaves. Kinetic changes at 820 nm reflect the redox states of P700 and PC. There is an initial oxidation of P700 and PC followed by a re-reduction when electrons arrive from PSII . After 40°C incubation, kinetic changes at 820 nm showed similar re-reduction of P700 and PC and this occurred after 20 ms. After 45°C incubation re-reduction kinetics of P700+ and PC+ were faster and occurred after 15 ms. On the other hand, after 50°C treatment re-reduction kinetics of P700+ and PC+ were much slower as observed in . From the maximal slopes of the kinetic curves of photoinduced MR changes, the rates of P700 and PC oxidation and the following re-reduction can be calculated.
(A) MR induced by red actinic light of 5000 µmol photons m−2 s−1 in pea leaves detached from the plants and dark-adapted for 1 h and heated to various temperatures (25, 30, 35, 40, 45 and 50°C) for 40 s in darkness. (B) Maximal slopes of the kinetics curve of photoinduced MR changes (the rates of P700 and PC oxidation and their followed re-reduction), the results are shown as the mean with standard deviations.
The temperature dependences of the values of the slopes are shown in Figure 7B. After 40 s incubation at room temperature, the calculated value of the P700 photooxidation relative rate was of about 2.3 ms−1 and for re-reduction –0.054 ms−1. The first value reflects the rate of photoinduced electron transfer through PSI and the second – the difference between the rates of electron donation by PSII towards PSI and acceptance of the electrons by PSI. Electron transfers from PSII to PQ, cytochrome (cyt) b6/f complex and PC were faster than those from PSI to Fd. The rate of P700 oxidation was slowed down by 20% after 40 s heating at 35°C and accelerated by 40% after 50°C. The P700+ reduction rate was increased by 22% after 45°C heating and inactivated by 33% after 50°C incubation.
PF, DF and MR signals show a distinct temperature response in pea leaves (Figure 2). An increase in the FK/FJ ratio indicates that heat treatment provokes an inhibition of the donation of electrons by the OEC . The lower electron transport rate through PSII after 45 and 50°C incubation changes DF induction (Figure 2) by showing a decrease in DF yield, which reflects the redox state of the PSII acceptors. Čjánek et al.  reported that at temperature above 40°C, the DF signal drops below the level observed at 35°C. Higher temperature of 45°C and 50°C cause a decrease in the peaks yields at I1 (7 ms) and I2 (100 ms), disappearance of DF decay from I1 to I2 and the disappearance of the I1 peak at 50°C. The disappearance of DF decay between the I1 and I2 peaks was in parallel to the disappearance of the J-I phase from the PF curve. In this phase (J-I) a progressive reduction of the plastoquinone (PQ) pool occurs  (see  for a discussion about the J-I-P thermal phase). The block of PSII reaction centers as well as the electron flow from the reduced QA to QB has been reported to be damaged at higher temperatures . Therefore, I1 to I2 decay might be related to the redox states of the PSII reaction center when the electron transfer from reduced QB to PQ begins.
DF decay kinetics is composed of several components denoted as LES . The increase and then the decrease of I2 (measured at 100 ms) may be related to the oxidation-reduction of the PQ-pool, which may be first activated by the increased temperature (due to the increased lipid fluidity of the thylakoid membranes that could lead to a higher diffusion rate of PQ molecules), and then it may be inactivated, probably because of protein disorganization at higher temperatures. The maximum I4 occurs in parallel with a decrease of the PF intensity. We noted here that I4 was less affected by heat treatment although after 50°C incubation its increase might be attributed to QA− accumulation.
We observed that the DF curves are more affected than PF curves at temperatures of 25, 30, 35 and 40°C. This may mean that DF curves are more thermosensitive than PF curves. Indeed, at these temperatures, we observed a decrease in the amplitude of the DF curve and change of I1, I2 and I3 peaks obtained from DF10–30 µs, while minor significant changes in PF curves were monitored. The relative I2 in the fast DF phase increased and the relative DF induction increased in the slow phase. The increase of relative DF in the slow phase might be related to the activation of the Calvin-Benson cycle (Figure 5). These observations have been reported by Zaharieva et al  when leaves of wild type and mutants of Arabidopsis were exposed to increased temperature to 45°C.
A decrease in FM (from 30°C) and increase in Fo (45°C) were observed. Increase of Fo has been suggested to be due to release of LHC II from the PS II complex and inactivation of PS II photochemical reaction , or an inhibition of electron flow from reduced QA to QB , . Yamane et al. ,  have also reported that the increase of Fo was also due to irreversible dissociation of LHC II from the PS II complex and partly reversible inactivation of PS II in spinach and rice. The decrease in the fluorescence FM level seemed to be related to denaturation of chlorophyll-proteins .
It is known that heat treatment leads to an inhibition of the donation of electrons by OEC, by a loss of the manganese cluster which leads to changes in the structure and function of PSII , , . Indeed, the K peak observed in the PF curve after 50°C treatment reflects this change by partial QA reduction, which is due to a stable charge separation resulting from the donation of one electron by tyrozine Z , . Therefore the absence of electron donors would lead to the accumulation of P680+. The decline of I1 to ∼3 ms observed in kinetics of fast DF components (measured at 10–30 µs delay-time) at 50°C occurred in parallel to the appearance of the K peak in the PF curve. We can assume that this decline might be related to the redox states of the PSII reaction center when the K step appeared in PF curve or in other words when OEC was destroyed. However, this decline can be related to the accumulation of P680+ and DF emission after recombination of LES P680+QA–. The absorption of only one light quantum is enough to form such a state. This is the reason for the short time for the appearance of this maximum. In dark–adapted state, samples start in 75% S1 and 25% So  and, therefore, the low luminescence state S1Z+QA–QB is formed before it is transformed to the high luminescence state S3Z+QA−QB; to complete this transformation, every RC needs to absorb two quanta for storing two electrons before donating them to the plastoquinone pool, PQ . Lazár  reported that the rise of fluorescence to the J step in the OJIP transient is much more suppressed when all OEC is initially in the S2 or S3 states and a new step appears in the OJIP transient located at the position of the K step. Using thermoluminescence (TL) method, an AG band peaking between 40 and 50°C has been observed , . This AG band emission is stimulated by high temperature, and corresponds to a heat-induced stimulation of electron transfer from stromal reductants to PSII centers that are initially in the non-recombining state S2/3QB and are progressively converted to light-emitting S2/3QB− states , .
Figure 6C shows a linear correlation between the FK/FJ and I2/I1 ratios. Indeed, this parameter FK/FJ was introduced by Srivastava and Strasser  in describing heated pea leaves. FK/FJ has been also introduced to monitor electron donation limitations on the donor side of PSII in barley varieties differing in their drought tolerance . The I2/I1 ratio has been used as an indication for electron flow acceleration through the PSII acceptor side . These two parameters (FK/FJ and I2/I1 ratios) might indicate the limitation of electron donation on the donor side of PSII and represent a quantitative measure for the inactivation of the PSII donor side. Therefore, they might be excellent parameters for monitoring heat stress effects on PSII.
Acceleration of P700+ and PC+ re-reduction was induced by 45°C treatment but after 50°C its reduction was slower, indicating PSI inhibition. However, many investigators have found that moderate heat stress increases PSI activity, often at the expense of the redox status of the stroma , . We note that PSI accelerates the oxidation rate at 50°C incubation with 80% as compared to that at 35°C (Figure 7B).
We are grateful to reviewers for their constructive comments and suggestions on the manuscript. We thank Prof. Govindjee for helpful comments on the manuscript and for his editing of the English text.
Conceived and designed the experiments: AO. Performed the experiments: AO. Analyzed the data: AO VG RJS. Wrote the paper: AO VG RJS.
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