Stress Tolerance of Photosystem II in Vivo: Antagonistic Effects of Water, Heat, and Photoinhibition Stresses

The in vivo photochemical activity of photosystem II was inferred from modulated chlorophyll fluorescence and photoacoustic measurements in intact leaves of several plant species (Lycopersicon esculentum Mill., Solanum tuberosum L., Solanum nigrum L.) exposed to various environmental stresses (drought, heat, strong light) applied separately or in combination. Photosystem II was shown to be highly drought-resistant: even a drastic desiccation in air of detached leaf samples only marginally affected the quantum yield for photochemistry in photosystem II. However, water stress markedly modified the responses of photosystem II to superimposed constraints. The stability of photosystem II to heat was observed to increase strongly in leaves exposed to water stress conditions: heat treatments (e.g. 42°C in the dark), which caused a complete and irreversible inhibition of photosystem II in well-watered (tomato) leaves, resulted in a small and fully reversible reduction of the photochemical efficiency of photosystem II in drought-stressed leaves. In vivo photoacoustic data indicated that photosystem I was highly resistant to both heat and water stresses. When leaves were illuminated with intense white light at 25°C, photoinhibition damage of photosystem II was more pronounced in water-stressed leaves than in undesiccated controls. However, in nondehydrated leaves, photoinhibition of photosystem II was strongly temperature dependent, being drastically stimulated at high temperatures above 38 to 40°C. As a consequence, when exposed to strong light at high temperature, photosystem II photochemistry was significantly less inhibited in dehydrated leaves than in control well-hydrated leaves. Our results demonstrate the existence of a marked antagonism between physicochemical stresses, with water stress enhancing the resistance of photosystem II to constraints (heat, strong light at high temperature) that are usually associated with drought in the field.     

Effect of Temperature on Photosynthetic Activities of Senescing Detached Wheat Leaves

Changes in various components of photosynthetic activity duringthe dark induced senescence of detached wheat leaves, maintainedat 25°C (control) and 35°C (mildly elevated temperaturetreatment), were examined. Senescence-associated decline measuredup to 96 h, in photosynthetic activity was appreciably hastenedat 35°C, than at 25°C as evident by the relative higherlosses of chlorophyll, photosystem (PS) II and PS I catalyzedphotochemical activities and ribulose-1,5-bisphosphate (RuBP)carboxylase activity. In addition, a comparatively higher risein light scattering profile of isolated chloroplasts was notedat 35°C than at 25°C. Senescence-induced degradationof chlorophyll was faster at 35°C than at 25°C; on theother hand, the degradation of carotenoids was faster at 25°Cthan at 35°C. Furthermore, the ratio of carotenoids to chlorophyllincreased with senescence up to 96 hours, higher ratio beingobtained at 35°C than at 25°C. Both PS II and PS I activitiesshowed a transient rise in the beginning phase of dark incubation,whereas loss in chlorophyll was continuous throughout the periodof senescence. The initial rise observed in photochemical activitieswas attributable to the uncoupling of electron transport fromphotophosphorylation. Elevated temperature treatment resultedin greater inactivation of RuBP carboxylase than control. Itappears that during senescence the loss in chlorophyll and RuBPcarboxylase activity are triggered simultaneously. (Received June 7, 1985; Accepted October 30, 1985)     

Studies on thermoluminescence,delayed light emission and oxygen evolution from photosynthetic materials: UV effects

The effect of ultraviolet light on thermoluminescence, oxygen evolution and the slow component of delayed light has been investigated in chloroplasts and Pothos leaves. All peaks including peak V (48°C) were inhibited by UV. However, the peak at 48°C which was induced by DCMU was enhanced following UV irradiation of chloroplasts at ambient temperature (23°C) whereas peak II (-12°C) and peak III (10°C) which were also induced by DCMU were inhibited. Chloroplasts treated with DCMU and dark incubated for several minutes at ambient temperature prior to recording of glow curves have also shown enhancement of peak at 48°C. A slow component of delayed light and photosystem II activity of chloroplasts were inhibited by UV whereas photosystem I activity was marginally affected. These results corroborate involvement of photosystem II in generating thermoluminescence and slow components of delayed light in photosynthetic materials.Abbreviations DCIP Dichlorophenol Indophenol - DCMU 3-(3,4-dichlorophenyl)-1,1-dimethylurea - DCQ 2,6 Dichloro-p-benzoquinone - DLE delayed light emission - MOPS Morpholino propane sulfonic acid - PSI Photosystem I - PS II Photosystem II - TL thermoluminescence     

Desiccation of the resurrection plant <Emphasis Type="Italic">Haberlea rhodopensis</Emphasis> at high temperature

Haberlea rhodopensis plants, growing under low irradiance in their natural habitat, were desiccated to air-dry state at a similar light intensity (about 30 μmol m⁻² s⁻¹) under optimal (23/20°C, day/night) or high (38/30°C) temperature. Dehydration of plants at high temperature increased the rate of water loss threefold and had a more detrimental effect than either drought or high temperature alone. Water deficit decreased the photochemical activity of PSII and PSI and the rate of photosynthetic oxygen evolution, and these effects were stronger when desiccation was carried out at 38°C. Some reduction in the amount of the main PSI and PSII proteins was observed especially in severely desiccated Haberlea leaves. The results clearly showed that desiccation of the homoiochlorophyllous poikilohydric plant Haberlea rhodopensis at high temperature had more damaging effects than desiccation at optimal temperature and in addition recovery was slower. Increased thermal energy dissipation together with higher proline and carotenoid content in the course of desiccation at 38°C compared to desiccation at 23°C probably helped in overcoming the stress.     

Photosynthesis and lipid composition of the Antarctic endemic rhodophyte Palmaria decipiens: effects of changing light and temperature levels

In coastal waters, Antarctic rhodophytes are exposed to harsh environmental conditions throughout the year, like low water temperatures ranging from −1.8°C to 2°C and high light during the summer season. Photosynthetic performance under these conditions may be affected by slowed down enzymatic reactions and the increased generation of reactive oxygen species. The consequence might be a chronic photoinhibition of photosynthetic primary reactions related to increased fragmentation of the D1 reaction centre protein in photosystem II. It is hypothesized that changes in lipid composition of biomembranes may represent an adaptive trait to maintain D1 turnover in response to temperature variation. The interactive effects of high light and low temperature were studied on an endemic Antarctic red alga, Palmaria decipiens, sampled from two shore levels, intertidal and subtidal, and exposed to mesocosm experiments using two levels of natural solar radiation and two different temperature regimes (2–5°C and 5–10°C). During the experimental period of 23 days, maximum quantum yield of photosynthesis decreased in all treatments, with the intertidal specimens exposed at 5–10°C being most affected. On the pigment level, a decreasing ratio of phycobiliproteins to chlorophyll a was found in all treatments. A pronounced decrease in D1 protein concentration occurred in subtidal specimens exposed at 2–5°C. Marked changes in lipid composition, i.e. the ratio of saturated to unsaturated fatty acids, indicated an effective response of specimens to temperature change. Results provide new insights into mechanisms of stress adaptation in this key species of shallow Antarctic benthic communities.     

Electron donor pool of photosystem II in Tris-washed chloroplasts in a study of low temperature delayed fluorescence

Transient time courses ("induction") and the intensity of thedelayed fluorescence of chlorophyll a (measured between 0.1and 3.9 msec after a 0.9 msec excitation period) were studiedwith a phosphoroscope at temperatures between 40 and –170°Cin Tris-washed chloroplasts. Tris-washing of chloroplasts changed the temperature dependenciesof the induction and the intensity of the delayed fluorescence.From the analysis of the induction each photosystem II reactioncenter appears to be linked to a donor pool which can supplyone electron to the acceptor pool in Tris-washed chloroplasts. An artificial electron donor, diphenylcarbazide affected thedelayed fluorescence above –100°C evidence that electronsare donated to photosystem II in at least two different ways. An electron transport inhibitor, 3-(3',4'-dichlorophenyl)-l,l-dimethylurea,changed the induction of the delayed fluorescence at temperaturesabove –60°C. The temperature dependence of the electron transport in thevicinity of photosystem II was characterized from these results. (Received May 27, 1980; )     

Two temperature-sensitive photosystem II mutants of pea

Two nuclear gene mutants of pea, chlorotica-887 and chlorina-5756, are temperature-sensitive in the development of photosystem II activity. Low temperature flourescence emission spectra of leaves show that the peak at 697 nm from the reaction center of photosystem II is present when the mutants have been grown at 18°C, but absent when they have been grown at 30°C. For leaves of chlorina-5756 grown at 18°C the relative size of the peak at 697 nm is reduced compared to that of leaves of the wild type or chlorotica-887 grown at this temperature. Flourescence induction curves of leaves from wild type plants and chlorotica-887 grown at 18°C possess two steps, while those of leaves from chlorina-5756 grown at 18°C or 30°C and chlorotica-887 grown at 30°C show at fast rise to the maximal level of fluorescence. Measurements on chloroplasts isolated from the mutants indicated that the photosystem I activity per g leaf material is comparable for plants grown at 18°C and plants grown at 30°C. In contrast, no photosystem II activity was detected when the mutants had been grown at 30°C. It is suggested that these mutants are affected in a component required for the assembly of functional photosystem II complexes.     

Chilling Damage to Photosynthesis in Young Zea mays: II. PHOTOCHEMICAL FUNCTION OF THYLAKOIDS IN VIVO

Leaves of Zea mays L. cv. LG11 were chilled for 6 h at 5 °Cin a high photon flux density. On return to 20 °C, the leavesshowed a 45% decrease in the apparent quantum yield of photosyntheticoxygen evolution. The effects of this chill-treatment on thechlorophyll fluorescence induction kinetics of the leaves indicateda 20–25% decrease in the primary photochemical quantumyield of photosystem II. The fluorescence emission spectra ofthese leaves demonstrated a marked modification in the distributionof excitation energy within the photochemical apparatus of thethylakoid membranes, such that photosystem I was excessivelyfavoured with respect to photosystem II. These chill-inducedchanges would result in an enhancement of cyclic over non-cyclicelectron transport and account for a decrease in the apparentquantum yield of photosynthetic oxygen evolution. Key words: Zea mays, Chilling, Photosynthesis, Thylakoids     

The Responsiveness to Temperature of the Extension Rates of Leaves of Wheat Growing in the Field under Different Levels of Nitrogen Fertilizer

The response of the rates of extension (LER) of wheat leaves(Triticum aestivum cv. Gamenya) to temperatures maintained fora short period was measured by changing the temperature of theextension zone and recording the changes in leaf length. Therange of temperatures used was from 4-38 °C. The LER ofall leaves responded to increases in temperature as field temperatureswere suboptimal. The data obtained from several series of measurementsover different ranges of temperature were combined to producea general response curve. The minimum temperature for LER wasconsidered to be approximately 0 °C, the optimum was 28.4°C, while the maximum was in excess of 38 °C. The responsivenessof LER to temperature, measured by the Q₁₀, declined exponentiallyfrom >6 at 5 °C to 2 at 20 °C. The Q₁₀ at 15 °Cwas not affected by nitrogen supply.     

Effect of cadmium on photosystem II activity in <Emphasis Type="Italic">Chlamydomonas reinhardtii</Emphasis>: alteration of O–J–I–P fluorescence transients indicating the change of apparent activation energies within photosystem II

In this study, we evaluated how cadmium inhibitory effect on photosystem II and I electron transport may affect light energy conversion into electron transport by photosystem II. To induce cadmium effect on the photosynthetic apparatus, we exposed Chlamydomonas reinhardtii 24 h to 0–4.62 μM Cd²⁺. By evaluating the half time of fluorescence transients O–J–I–P at different temperatures (20–30°C), we were able to determine the photosystem II apparent activation energies for different reduction steps of photosystem II, indicated by the O–J–I–P fluorescence transients. The decrease of the apparent activation energies for PSII electron transport was found to be strongly related to the cadmium-induced inhibition of photosynthetic electron transport. We found a strong correlation between the photosystem II apparent activation energies and photosystem II oxygen evolution rate and photosystem I activity. Different levels of cadmium inhibition at photosystem II water-splitting system and photosystem I activity showed that photosystem II apparent activation energies are strongly dependent to photosystem II donor and acceptor sides. Therefore, the oxido-reduction state of whole photosystem II and I electron transport chain affects the conversion of light energy from antenna complex to photosystem II electron transport.     

Influence of heat shock on chlorophyll fluorescence of white oak (<Emphasis Type="Italic">Quercus pubescens</Emphasis> Willd.) leaves

Chlorophyll fluorescence parameters of Quercus pubescens Willd. as response to heat shock (HS) by immersing leaves for 5 and 15 min in water of temperatures between 38 and 59 °C were examined. Fluorescence was measured after different periods of recovery (15, 30, 90, 210, and 1 440 min at 24/26 °C night/day temperature and 100 % humidity). The effective quantum yield of photosystem 2 (Y) in control and HS-treated leaves was always measured after previous 15 min irradiation. Under a 5 min HS, Y did not change after using temperatures below 44 °C, was rapidly restored after HS of moderate temperatures (44–48 °C), and progressively decreased and recovered eventually to the initial value after HS of high temperatures (48–52 °C). Y did not recover after HS with temperatures higher than 52 °C. Increase in the duration of HS from 5 to 15 min lead to change of the initial Y at each HS temperature, but the recovery processes were similar to those characteristic after 5 min incubation. The processes of recovery may depend mainly on the specificity of injuries caused by different heat shock temperatures. Thus Q. pubescens is able to preserve and recover the functional potential of its photosynthetic apparatus in response to HS up to 52 °C.     

Short term acclimation of spinach to high temperatures: effect on chlorophyll fluorescence at 293 and 77 Kelvin in intact leaves

Using intact leaves of Spinacia oleracea (L.), reversible temperature-induced changes in chlorophyll fluorescence emitted at room temperature and at 77K were studied. Interpretation of fluorescence at 77K was largely facilitated by developing a new method to minimize reabsorption artifacts (`diluted leaf-powder'). Leaves of plants grown at 15 to 20°C were exposed for several hours to different temperatures. Upon incubation at 35°C in the dark or in the light, the following changes in 77K fluorescence occurred with a half-time of less than 1 hour: (a) the initial fluorescence (F₀) of photosystem I increased by 15%, while that one of photosystem II somewhat decreased; (b) although variable fluorescence declined in both photosystems, the decrease in photosystem II (40%) was more severe; (c) the changes were less significant after 480-nanometer excitation light was replaced by 430-nanometer light. The data were interpreted in terms of a reversible, temperature-induced change in thylakoid structure and related change in the distribution of the absorbed energy in favor of photosystem I, at the expense of photosystem II excitation, probably accompanied by an increase in the rate of thermal deactivation of excited states. The considerable decrease in the variable part of room temperature fluorescence gives rise to the suggestion that this transition has lowered the reduction level of plastoquinone, i.e. has increased electron flow through photosystem I, relative to photosystem II. Possible physiological and mechanistic analogies between this temperature-induced state transition and the light-dependent state 1-state 2 regulation has been discussed.     

Carotenoids and fatty alcohols as non-ionic hydrophobic inhibitors of photochemical activities of chioroplasts

Carotenoids and fatty alcohols were added to intact spinachchloroplasts in suspension, and the effects of these reagentson the absorption spectrum and photochemical activities of chloroplastswere examined. The addition of lutein, ß-caroteneand neoxanthin transformed a chlorophyll a form (C684) havingan absorption maximum at 684 nm into C666, and the activityof photosystem II decreased parallel with this transformation.The activity of photosystem I was completely unaffected by theeffect of added carotenoids, whereas both cyclic and non-cyclicphotophosphorylations were inhibited by the additions. Theseeffects were reproducibly observed only with a "petroleum ether-soluble"fraction of each carotenoid, monomeric and less polymerizedforms, which are soluble in petroleum ether at –25°C;the "insoluble" fraction of more polymerized forms was ineffective.Comparative experiments with lutein, DCMU and CCCP as inhibitorsand the dependence of inhibition on light intensity suggestedthat the site of inhibition by carotenoids is on the water sideof photosystem II between its reaction center and the CCCP-inhibitingsite. Fatty alcohols with carbon atoms between 8 and 12 producedstronger but less specific effects on the spectrum and activities.At low concentrations the uncoupling of photophosphorylationoccurred and, in a middle concentration range, the activityof photosystem II decreased with the transformation of C684into C666 and with a change in carotenoid bands. At higher concentrations,where the enhanced activity of photosystem I decreased froma maximum to zero, the red band of chlorophyll a further changedin a complex manner and the absorption around 503 nm decreased.We, thus, deduced that C684 and some endogeneous carotenoidsare associated with photosystem II on its water side and thatadded carotenoids and fatty alcohols at lower concentrationschange their states, resulting in the inhibition of this photosystem. (Received December 20, 1971; )     

Temperature Dependence of Photosynthesis in Agropyron smithii Rydb. : II. CONTRIBUTION FROM ELECTRON TRANSPORT AND PHOTOPHOSPHORYLATION

As part of an analysis of the factors regulating photosynthesis in Agropyron smithii Rydb., a C₃ grass, the response of electron transport and photophosphorylation to temperature in isolated chloroplast thylakoids has been examined. The response of the light reactions to temperature was found to depend strongly on the preincubation time especially at temperatures above 35°C. Using methyl viologen as a noncyclic electron acceptor, coupled electron transport was found to be stable to 38°C; however, uncoupled electron transport was inhibited above 38°C. Photophosphorylation became unstable at lower temperatures, becoming progressively inhibited from 35 to 42°C. The coupling ratio, ATP/2e⁻, decreased continuously with temperature above 35°C. Likewise, photosystem I electron transport was stable up to 48°C, while cyclic photophosphorylation became inhibited above 35°C. Net proton uptake was found to decrease with temperatures above 35°C supporting the hypothesis that high temperature produces thermal uncoupling in these chloroplast thylakoids. Previously determined limitations of net photosynthesis in whole leaves in the temperature region from 35 to 40°C may be due to thermal uncoupling that limits ATP and/or changes the stromal environment required for photosynthetic carbon reduction. Previously determined limitations to photosynthesis in whole leaves above 40°C correlate with inhibition of photosynthetic electron transport at photosystem II along with the cessation of photophosphorylation.     

Formation of early-light-inducible-protein complexes and status of xanthophyll levels under high light and cold stress in barley (Hordeum vulgare L.)

In our previous work we found considerable accumulation of early light-inducible proteins (ELIPs) in barley during adaptation to combined high light and cold stress, an accumulation which occurred preferentially in the apical part of the leaves (M.-H. Montané et al., 1997, Planta 202: 293–302). Here we studied, under the same conditions, the effect of adaptation on the composition of thylakoid membrane proteins and pigments, particularly xanthophylls and chlorophyll, and their distribution within the barley leaf. It was observed that high light fluxes appeared to favour the trimerization of the light-harvesting complex of photosystem II (LHC II) whereas cold appeared to favour the monomers of LHC II. High light, cold or the combination of both factors had only a small effect on the protein composition of the thylakoid membranes except for the proteins of LHC II which were found to decrease under high light to a greater extent at 25 °C than at 5 °C. The total xanthophyll-cycle carotenoid content increased linearly with cellular development, the highest amount being observed in the apical part of the leaf. Cold and high light acted synergistically to induce less than a doubling in the amount of total xanthophylls, while chlorophylls a and b remained nearly constant. The fraction consisting of antheraxanthin plus zeaxanthin was up to 4- to 5-fold higher at 5 °C than at 25 °C. As determined previously (Montané et al. 1997), the same conditions caused a 15-fold increase in the accumulation of ELIPs. Consequently, neither the distribution of total xanthophylls nor that of antheraxanthin plus zeaxanthin along the leaf followed the same pattern as ELIP. Thus, the accumulation of xanthophylls cannot be stoichiometrically correlated with that of ELIPs. Using electrophoresis in the presence of decylmaltoside, we could demonstrate for the first time that ELIPs of 13.5 kDa are contained in high-molecular-mass complexes of >100 kDa, which are located in the unstacked stroma lamellar region of the thylakoid membranes. Received: 6 April 1998 / Accepted: 26 January 1999     

Changes in the Distribution of 14C-Labelled Assimilates in Sugar-beet with Variation of Temperature

Plants were allowed to assimilate ¹⁴CO₂ for 30 min at 5, 15,25, and 35 °C. The changes in ¹⁴C content of a mature expandedleaf (Leaf 4), young apical leaves, and storage root, were sequentiallyfollowed over a subsequent period of 24 h in continuous light.In a second experiment plants were transferred after ¹⁴CO₂ assimilationto temperatures of 10, 18, 26, and 34 °C, and the partitionof ¹⁴C between the ethanol-soluble and ethanol-insoluble fractionsof the roots and leaves was followed over a period of 72 h. The specific activities of the apical leaves and of the storageroot increased to a maximum 2 h after labelling at 25 °C,4 h at 15 and 35 °C, and 6 h at 5 °C suggesting thatthe optimum temperature for translocation of photosynthate wasabout 25 °C. The ¹⁴C partition to ethanol-soluble and ethanol-insoluble fractionsof the roots and leaves was largely attained in. 9 h. Littlerepartition of ¹⁴C assimilate fractions occurred as a resultof temperature change or growth. Root ethanol-insoluble activity,however, did increase significantly over the 72-h period : possiblecauses of this slow incorporation and their relevance to themechanism of sugar storage are discussed.     

Effects of Light and Temperature on Flower-opening of Pharbitis nil

Flower buds of Pharbitis nil cut from plants growing in thefield opened rapidly when kept in darkness for 8 hr followedby continuous light at 20–25°C, but those kept indarkness for 4 hr opened promptly oniy when the temperatureduring the following light period was kept at 23°C or lower.Buds exposed to continuous light at 25°C did not open, butthose exposed to continuous light at 23°C opened slowly.At a lower temperature, the buds opened rapidly even in continuouslight. When the buds were placed in darkness at 25°C at13:30, 17:30 and 21:30 (artificial light from 17:30 to 21:30),they opened about 10 hr after the onset of darkness regardlessof the time of the onset of darkness, but when the buds werekept at 20°C in light from 13:30, 17:30 and 21:30, theyopened at 3:30–5:30 regardless of the time of transferto the lower temperature. The biological clock which controlsthe time of flower-opening is suggested to be easily reset bya light-off signal, but not by a shift from a normal to lowertemperature (20°C). At the lower temperature, the time offlower-opening probably is determined by the time of the latestpreceding light-off (or light-on) signal. ¹Dedicated to Professor Dr. Erwin Biinning on the occasion ofhis 75th birthday. (Received October 23, 1980; Accepted December 15, 1980)     

Analysis of the Heat Stress Induced Quenching of Variable Chlorophyll a Fluorescence in Beet Spinach Leaves: Possible Accumulation of Oxidized Quencher P680+ under High Illumination

Effect of preheating of beet spinach leaves on chlorophyll a fluorescence yield was analyzed with the help of additional high intensity illumination pulses using a pulse modulated fluorometer. Preheating at mildly elevated temperature (35–45°C) causes a shift in the redox state of secondary donor of photosystem II, possibly due to uncoupling of phosphorylation because of thermal induced membrane disorganization and associated alkalinization of intra thylakoid space. Also, at these preheating temperatures, a rise in photosystem I catalyzed electron transfer has been shown to occur. These two effects induce rapid quenching of Chi a fluorescence, which drops even in the presence of actinic light, below the level of initial fluorescence (F_o′ monitored by the weak modulated probing light. Preheating of leaf segments induces an increase in fluorescence in the presence of dluron, which blocks electron flow between two photosystems, and thus this increases in fluorescence yield (F_o′ as monitored by weak modulated light, is not solely due to disorganization of light harvesting Chi-protein complex but also due to a shift in the redox equilibrium of the donor at the oxidizing side of photosystem II resulting in rapid reduction of Q_A the stable primary acceptor of photosystem II. In 50°C preheated DCMU treated samples, the fluorescence yield increases in weak modulated light and it approaches that of maximal steady state (F_max) level. At preheating temperature of 48°–50°C, the inactivation of enzymes in the reducing side of photosystem I, causes an impairment of the reoxidation of QA and under this condition, a strong illumination causes quenching of Chi a fluorescence. This quenching seems to arise because of accumulation of the P680⁺, the oxidized physiological donor of photosystem which is a quencher of Chi a fluorescence. This quenching depended on the pulse intensity and duration which saturates P680⁺ accumulation and is greatly manifested when water oxidation complex is damaged.     

Temperature-Induced Changes of Variable Fluorescence-Yield in Intact Leaves

Variable fluorescence (F_v) of intact leaves was measured whenthe temperature was lowered at a rate of 1–2?C per mn,from 20?C to –20?C. The quantum flux density of the excitinglight was 1–2 µE m^–2 sec^–1 in orderto sensitize F only at 20?C. The fluorescence yield decreasedrapidly at the freezing point of the leaf and upon further coolingthe fluorescence yield increased again. F_m was obtained a fewdegrees below the freezing point. Repeated freeze-thaw cycles caused successively increased damageto the thylakoid membranes on either the oxidizing or the reducingside of photosystem II. An eventual loss of F_v over F_o was typicalfor damage on the water splitting side of photosystem II, whereasdamage after the primary electron acceptor Q of photosystemII was characterized by an invariable fluorescence yield atF_m over the temperature range examined. (Received January 18, 1982; Accepted June 12, 1982)