Effects of manganese toxicity on photosynthesis of white birch (Betula platyphylla var. japonica) seedlings

The effects of manganese (Mn) toxicity on photosynthesis in white birch ( Betula platyphylla var. japonica ) leaves were examined by the measurement of gas exchange and chlorophyll fluorescence in hydroponically cultured plants. The net photosynthetic rate at saturating light and ambient CO₂ (C_a) of 35 Pa decreased with increasing leaf Mn concentrations. The carboxylation efficiency, derived from the difference in CO₂ assimilation rate at intercellular CO₂ pressures attained at C_a of 13 Pa and O Pa, decreased with greater leaf Mn accumulation. Net photosynthetic rate at saturating light and saturating CO₂ (5%) also declined with leaf Mn accumulation while the maximum quantum yield of O₂ evolution at saturating CO₂ was not affected. The maximum efficiency of PSII photochemistry (F_v/F_m) was little affected by Mn accumulation in white birch leaves over a wide range of leaf Mn concentrations (2–17 mg g₋₁ dry weight). When measured in the steady state of photosynthesis under ambient air at 430 μmol quanta m₋₂ s₋₁, the levels of photochemical quenching (qP) and the excitation capture efficiency of open PSII (F'^v/F'^m) declined with Mn accumulation in leaves. The present results suggest that excess Mn in leaves affects the activities of the CO² reduction cycle rather than the potential efficiency of photochemistry, leading to increases in Q_A reduction state and thermal energy dissipation, and a decrease in quantum yield of PSII in the steady state.     

A precise potentiometric method for determination of algal activity in an open CO2 system

Abstract. The activity of the green alga Scenedesmus obliquus was studied in simplified nutrient solutions (20 mol m₋₃ NaNO₃, 20 mol m₋₃ NH₄C1, 20 mol m₋₃ NH₄NO₃, and 20 mol m₋₃ NaCl, respectively) at 25 °C. The experiments were performed under welldefined incident photon density fluxes ranging from 10 to 200 μmol m₂ s₋₁, Light-dependent changes in pH and alkalinity (A) were followed by means of a potentiometric method using a glass electrode. In the experiments, carbon dioxide with known partial pressure was bubbled through the algal suspension, and during dark periods ul intervals of 1 h, the solution was allowed to equilibrate with the gas phase. This technique was applied to calculate equilibrium values of pH and alkalinity at regular intervals during a 12-h period. Results obtained in NaNO₃, solution show a linear increase in A with time, at each level of illumination studied. After an initial drop, A also increases in NH₄NO₃, solution in a similar way to that in NaNO₃ solution. The change in A with time was also found to increase linearly with the photon density flux studied and no saturation level could be defined. In experiments in NaCl solution, no changes in A were registered while measurements in NH₄Cl solution showed a decrease in A with time.     

Gas exchange parameters, water relations and carbohydrate partitioning in leaves of field-grown Prunus domestica following fruit removal

The effect of fruit removal on gas exchange, water relations, chlorophyll and non-structural carbohydrate content of leaves from mature, field-grown plum trees ( Prunus domestica L. cv. Stanley) was determined over 2 consecutive growing seasons. Removal of fruits during stage II of fruit development decreased CO₂ assimilation rate within 24 h from 12.6 to 8.5 μmol m^-2 s^-1 in 1986, and from 12.1 to 10.2 μmol m^-2 s^-1 in 1987. Depression of net photosynthesis persisted for at least 5 days and was greatest in the early afternoon. Recovery of the CO₂ assimilation rate to pretreatment levels coincided in defruited trees with vegetative growth that was more than 5-fold that of fruiting trees in the first 6 weeks after fruit removal in 1986. Estimated photorespiration was similar in both fruiting and defruited trees. The stomatal contribution to the decrease of CO₂ assimilation rate, calculated from assimilation/intercellular CO₂ curves, ranged from 31 to 46%. Defruiting did not affect leaf water potential, but decreased leaf osmotic potential. Leaf levels of chlorophyll, fructose, glucose, sorbitol and sucrose were not affected by defruiting, whereas starch content increased up to 51% in leaves of defruited trees within 24 h after fruit removal. However, because of the small starch pool present in plum leaves (<1.9% dry weight) it is unlikely that starch accumulation was responsible for the observed decline in CO₂ assimilation rate after fruit removal. The decrease of CO₂ assimilation rate is discussed in relation to the hypothesis of assimilate demand regulating photosynthesis through a feedback mechanism.     

Photosynthesis and transpiration by young Larix kaempferi trees: C3 responses to light and temperature

The effects of photon flux density and temperature on net photosynthesis and transpiration rates of mature and immature leaves of three-year-old Japanese larch Larix kaempferi (Lamb.) Sarg. trees were determined with an infrared, differential open gas analysis system. Net photosynthetic response to increasing photon flux densities was similar for different foliage positions and stage of maturity. Light compensation was between 25 and 50 μmol m⁻² s⁻¹. Rates of photosynthesis increased rapidly at photon flux densities above the compensation level and became saturated between 800 and 1000 μmol m⁻² s⁻¹. Transpiration rates at constant temperature likewise increased with increasing photon flux density, and leveled off between 800 and 1000 μmol m⁻² s⁻¹. Photosynthetic response to temperature was determined in saturating light and was similar for all foliage positions; it increased steadily from low temperatures to an optimum range betweeen 15 and 21°C and then decreased rapidly above 21°C. Transpiration rate, however, increased continuously with rising temperature up to the experimental maximum. CO₂ compensation concentrations for mature foliage varied between 58 and 59 μl l⁻¹; however, foliage borne at the apex of the terminal leader compensated at 75 μl l⁻¹. None of these data support the claim that Japanese larch possesses C₄ photosynthetic characteristics.     

Stomatal and photosynthetic responses to shade in sorghum, soybean and eastern gamagrass

We studied photosynthetic and stomatal responses of grain sorghum ( Sorghum bicolor [L.] Moench cv. Pioneer 8500), soybean ( Glycine max L. cv. Flyer) and eastern gamagrass ( Tripsacum dactyloides L.) during experimental sun and shade periods simulating summer cloud cover. Leaf gas exchange measurements of field plants showed that short-term (5 min) shading of leaves to 300–400 μmol m⁻² s⁻¹ photosynthetic photon flux density reduced photosynthesis, leaf temperature, stomatal conductance, transpiration and water use efficiency and increased intercellular CO₂ partial pressure. In all species, photosynthetic recovery was delayed when leaves were reilluminated, apparently by stomatal closure. The strongest stomatal response was in soybean. Photosynthetic recovery was studied further with soybeans grown indoors (maximum photosynthetic photon flux density 1 200 μmol m⁻² s⁻¹). Plants grown indoors had responses to shade similar to those of field plants, except for brief nonstomatal limitation immediately after reillumination. These responses indicated the importance of the light environment during leaf development on assimilation responses to variable light, and suggested different limitations on carbon assimilation in different parts of the soybean canopy. Photosynthetic oxygen evolution recovered immediately upon reillumination, indicating that the light reactions did not limit soybean photosynthetic recovery. While shade periods caused stomatal closure and reduced carbon gain and water loss in all species, the consequences for carbon gain/water loss were greatest in soybean. The occurrence of stomatal closure in all three species may arise from their shared phenologies and herbaceous growth forms.     

A developmental study of Glycine max cell and protoplast isolation in relation to leaf age and photosynthetic competence

Leaf mesophyll cells were isolated from developing first trifoliate leaves of Glycine max (L.) Merr cv. Fiskeby V using a mechanical isolation procedure combined with low speed centrifugation. Cell yields of 17 ± 1.7% were routinely obtained with 55–75% intactness, as assessed by staining techniques, fluorescence transients and the ability of cells to convert to protoplasts after enzyme treatment. Rates of leaf photosynthesis were maximal in 27-day-old plants [280 μmol O₂ evolved (mg chlorophyll)^-1h^-1], from which isolated cells and protoplasts gave rates of up to 140 μmol O₂ evolved (mg chlorophyll)^-1 h^-1. Results are discussed in relation to leaf development and cell status during the attainment of photosynthetic competence.     

Development of leaf thickness for Plectranthus parviflorus – Influence of photosynthetically active radiation

Photosynthetically active radiation (PhAR) is apparently the environmental factor having the greatest influence on leaf thickness for Plectranthus parviflorus Henckel (Labiatae). A four-fold increase in leaf thickness from 280 to 1170 μm occurred as the PhAR was raised from 1.3 to 32.5 mol m⁻² day⁻¹. Compared to a constant PhAR of 2.5 mol m⁻² day⁻¹, a PhAR of 32.5 mol m⁻² day⁻¹ for one week during the first week (with return to 2.5 mol m⁻² day⁻¹ during the second and third weeks) led to an increase in final leaf thickness by 323 μm (to 802 μm). When increased PhAR was applied during the second week the increase in final thickness over the control was 217 μm, and when increased PhAR was applied during the third week it was 99 μm. However, leaf thickness was not simply responding to total daily PhAR, since a leaf 450 μm thick could occur at a low instantaneous PhAR for a long daytime (total daily PhAR of 1.5 mol m⁻² day⁻¹) and at a high PhAR for a short daytime (4.5 mol m⁻² day⁻¹). Total daily CO₂ uptake (net photosynthesis) was approximately the same in the two cases, suggesting that this is an important factor underlying the differences in leaf thickness. Leaf thickness is physiologically important, since thicker leaves tend to have greater mesophyll surface area per unit leaf area ( A ^mes/ A ) and hence higher photosynthetic rates.     

Photosynthesis, growth and structural characteristics of holm oak resprouts originated from plants grown under elevated CO2

The physiological characteristics of holm oak ( Quercus ilex L.) resprouts originated from plants grown under current CO₂ concentration (350 μl l⁻¹) (A-resprouts) were compared with those of resprouts originated from plants grown under elevated CO₂ (750 μl l⁻¹) (E-resprouts). At their respective CO₂ growth concentration, no differences were observed in photosynthesis and chlorophyll fluorescence parameters between the two kinds of resprout. E-resprouts appeared earlier and showed lower stomatal conductance, higher water-use efficiency and increased growth (higher leaf, stem and root biomass and increased height). Analyses of leaf chemical composition showed the effect of elevated [CO₂] on structural polysaccharide (higher cellulose content), but no accumulation of total non-structural carbohydrate on area or dry weight basis was seen. Four months after appearance, downregulation of photosynthesis and electron transport components was observed in E-resprouts: lower photosynthetic capacity, photosystem II quantum efficiency, photochemical quenching of fluorescence and relative electron transport rate. Reduction in ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBisCo) activity, deduced from the maximum carboxylation velocity of RuBisCo, accounts for the observed acclimation. Increased susceptibility of photosynthetic apparatus to increasing irradiance was detected in E-resprouts.     

Photosynthetic response of Eragrostis tef to temperature

Photosynthetic characteristics of leaves of tef, Eragrostis tef (Zucc.) Trotter, plants, grown at 25/15°C (day/night), were measured at temperatures from 18 to 48°C. The highest carbon exchange rates (CER) occurred between 36 and 42°C. and averaged 27 μmol m⁻² s⁻¹. At lower or higher temperatures, CER was reduced, but the availability of CO₂ to the mesophyll, measured as internal CO₂ concentration, was highest when temperatures were above or below the optimum for CER. In addition, CER and stomatal conductance were not correlated, but residual conductance was highly correlated with CER (r = 0.98). In additional experiments, relative ¹³C composition for leaf tissue grown at 25, 35 and 45°C averaged -14.4 per mille, confirming that tef is a C₄ grass species. Dry matter accumulation was higher at 35 than at 25, and lowest at 45°C. Leaf CER rates increased hyperbolically with increased light when measured from 0 to 2000 μmol m⁻² s⁻¹ PPFD. The highest CER, 31.8 μ-mol m_-2 s⁻¹, occurred at 35°C and 2000 μmol m⁻² s⁻¹ PPFR. At high light, CER at 25 and 35°C were nearly equal because of higher stomatal conductance at 25°C. Residual conductance was, however, clearly highest at 35°C compared to 25 and 45°C treatments. Stomatal conductance and residual conductance were not correlated in either set of experiments, yet residual conductance was always highest when temperatures were between 35 and 42°C across experiments, suggesting that internal leaf photosynthetic potential was highest across that temperature range.     

Measuring and modelling environmental influences on photosynthetic gas exchange in Sphagnum and Pleurozium

A mechanistic model has been used to examine the environmental regulation of photosynthetic gas exchange in moss. The effects of water content on conductance to CO₂ and on photosynthetic capacity during desiccation were calculated from the carbon isotope discrimination data of Williams & Flanagan (1996 , Oecologia 108, pp. 38–46) and combined with the biochemical model of Farquhar et al. (1980 , Planta 149, pp. 78–90). The model includes a simple light attenuation function that imparts curvature to the light response curve for net assimilation, enabling the use of physiologically realistic values for the biochemical parameters. Measurements of gas exchange for Sphagnum and Pleurozium were made in an old black spruce ecosystem over a growing season in order to assign values to parameters in the model. The calculated maximum rates of carboxylation by Rubisco ( V _max) were 5, 14 and 6 μ mol m^–2 s^–1 for Sphagnum during the spring, summer and autumn seasons of 1996, respectively. The increase in V _max during the summer was consistent with an increased allocation of resources to the photosynthetic apparatus. In contrast, no seasonal variation in V _max was observed in Pleurozium with average values of 7, 5 and 7 μ mol m^–2 s^–1 during the spring, summer and autumn, respectively.     

Diurnal variations of photosynthesis and dew absorption by leaves in two evergreen shrubs growing in Mediterranean field conditions

The effects of summer drought, dew deposition on leaves and autumn rainfall on plant water relations and diurnal variations of photosynthesis were measured in two evergreen shrubs, rosemary ( Rosmarinus officinalis ) and lavender ( Lavandula stoechas ), grown in Mediterranean field conditions. Withholding water for 40 d caused a similar decrease in predawn shoot water potential (ψ_pd) from c. −0.4 to c. −1.3 MPa in both species, but a 50% decrease in the relative leaf water content in L. stoechas compared with 22% in R. officinalis . A similar decrease in CO₂ assimilation rates by c. 75% was observed in water-stressed plants of both species, although L. stoechas showed smaller photosynthesis: stomatal conductance ratio than R. officinalis (35 vs 45 μmol CO₂:mol H₂O). The relative quantum efficiency of photosystem II photochemistry also decreased by c. 45% at midday in water- stressed plants of both species. Nevertheless, neither L. stoechas nor R. officinalis suffered drought-induced damage to photosystem II, as indicated by the maintenance of the ratio F _v: F _m throughout the experiment, associated with an increase in the carotenoid content per unit of chlorophyll by c. 62% and c. 30%, respectively, in water-stressed plants. Only L. stoechas absorbed dew by leaves. In this species the occurrence of 6 d of dew over a 15-d period improved relative leaf water content by c. 72% and shoot water potential by c. 0.5 MPa throughout the day in water-stressed plants, although the photosynthetic capacity was not recovered until the occurrence of autumn rainfall. The ability of leaves to absorb dew allowed L. stoechas to restore plant water status, which is especially relevant in plants exposed to prolonged drought.     

CO2 enrichment, drought stress and growth of Alaska pea plants (Pisum sativum)

The interaction of CO₂ enrichment and drought on water status and growth of pea plants was investigated. Pisum sativum L. (cv. Alaska) plants were grown from seeds in growth chambers using 350 and 675 μl I1 CO₂, a photon flux density of 600 μmol M-2 S-1, a 16 h photoperiod and a temperature regime of 20/14°C. The drought treatment was started at the beginning of branch initiation and lasted for 9 or 11 days. The water status of the plants was monitored daily by measuring total leaf water potential and stomatal conductance. The total leaf water potential of well-watered plants was not affected by the CO₂ level. Under draughting conditions total leaf water potential decreased, with a slower decrease under the high CO₂ regime, due, at least in part, to reduced stomatal conductance. Upon rewatering, total leaf water potential and stomatal conductance recovered within one day. High CO₂ counteracted the reduction in height and, to some extent, leaf area that developed in low CO₂ unwatered plants. Additional CO₂ had no effect on branch number and did not prevent the complete inhibition of branch development that resulted from drought stress. Removing the drought conditions resulted in a rapid recovery of the internal water status and also a rapid recovery of most, but not all, plant growth parameters.     

Long-term effects of low levels of SO2 on bean plants (Phaseolus vulgaris). I. Immission-response pattern of net photosynthesis and transpiration during life-long, continuous measurements

The immission-response effect of five low levels of sulfur dioxide on net photosynthesis and transpiration was studied during continuous measurements in near-complete life cycles of whole bean plants ( Phaseolus vulgaris L. cv. Processer) grown in a controlled environment. Sixteen plants were grown in individual water cultures in each of five 100 1 glass assimilation chambers with a new type of exposure system with separate root aeration. SO₂ immission ranged from 10 μg m⁻³ to 950 μg m⁻³ during 12-h day-time exposure periods, five days a week, while a low, natural background of NO_x was accepted.
The SO₂-induced photosynthetic reductions were in the short term, but in particular on the long-term level very closely related with stomatal conductance (significance level better than 0.0005). However, a causal coherence was not inferred. Physiological inhibitions were composed of: (1) A reversible component (night and week-end recovery) and (2) an irreversible component (related to reduced green leaf area). The pattern of leaf growth was studied, with the conclusion that SO₂ reduced leaf area by promoting senescence, rather than by interfering with leaf emergence and development.     

Responses of apple leaf stomata to environmental factors

Abstract. Stomatal conductances ( g _s) were measured on the leaves of 3–4 year old Golden Delicious trees and of seedlings of two other cultivars. Measurements were made on container grown trees in the field with a diffusion porometer in 1975 and 1976, and in controlled conditions in a leaf chamber in the laboratory in 1976. Stomatal densities in the Golden Delicious leaves were assessed from scanning electron micrographs. Stomatal density on extension shoot leaves was higher than on other leaf types after June.
The response to irradiance shown by both the porometer and the leaf chamber results could be described by a rectangular hyperbola: where g _max is maximum conductance and β indicates the sensitivity of g_s to photon influx density ( Q _p). The values of β were in the range 60–90 μmol m⁻² s⁻¹.
There was no evidence that apple stomata are sensitive to temperature per se, but g _s was reduced by increasing leaf to air vapour pressure deficits ( D ). There was a linear relationship between g _s and D which was not attributable to feed-back to leaf water potential (ψ_L) as the latter did not affect g _s until a threshold of about −2.0 to −2.5 MPa was reached. Conductance generally declined with increasing ambient CO₂ concentration.     

Effect of light and gibberellic acid on photosynthesis during leaf senescence of alstroemeria cut flowers.

The functioning of the photosynthetic apparatus during leaf senescence was investigated in alstroemeria cut flowers by a combination of gas-exchange measurements and analysis of in vivo chlorophyll fluorescence. Chlorophyll loss in leaves of alstroemeria cut flowers is delayed by light and by a treatment of the cut flowers with gibberellic acid (GA₃). The maximal photosynthesis of the leaves was approximately 6 μmol CO₂ m⁻² s⁻¹ at I 350 μmol m⁻² s⁻¹ (PAR) which is relatively low for intact C₃ leaves. Qualitatively the gas-exchange rates followed the decline in chlorophyll content for the various treatments, i.e. light and GA₃-treatment delayed the decline in photosynthetic rates. However, when chlorophyll loss could not yet be observed in the leaves, photosynthetic rates were already strongly decreased. In vivo fluorescence measurements revealed that the decrease in CO₂ uptake is (partly) due to a decreased electron flow through photosystem II. Furthermore, analysis of the fluorescence data showed a high nonphotochemical quenching under all experimental conditions, indicating that the consumption of reducing power in the Calvin cycle is very low. The chlorophyll, remaining after 9 days incubation of leaves with GA₃ in the dark should be considered as a 'cosmetic' pigment without any function in the supply of assimilates to the flowers.     

Regulation of the photosynthetic capacity of primary bean leaves by the red:far-red ratio and photosynthetic photon flux density of incident light

The main objective of the present work was to examine the effects of the red:far-red ratio (R:FR) prevailing during leaf development on the photosynthetic capacity of mature leaves. Plants of Phaseolus vulgaris L. cv. Balin de Albenga were grown from time of emergence in a controlled environment room, 25 ± 3°C, 12-h photoperiod, with different light treatments:a) high photosynthetic photon flux density (PPFD) = 800 μmol m⁻¹ s⁻¹+ high R:FR= 1.3;b) low PPFD= 300 μmol m⁻² s⁻¹+ high R:FR= 1.3; c) high PPFD=800 μmol m⁻² s⁻¹+ low R:FR= 0.7; d) low PPFD= 300 μmol m⁻²s⁻¹+ low R:FR=0.7. With an R:FR ratio of 1.3, a decrease in irradiance during leaf growth reduced photosynthesis when measured at moderate to high PPFD; but when measured at low PPFD, leaves expanded under low irradiance actually had photosynthesis rates higher than those of leaves grown in high irradiance. A low R:FR ratio during development reduced the photosynthetic capacity of the leaves. In leaves expanded under R:FR = 0.7 and high irradiance photosynthesis was reduced by 42 to 89%, depending on the PPFD at which measurements were made, whereas for leaves developed at R:FR = 0.7 and low irradiance photosynthesis decreased by 21 to 24%, compared to leaves under R:FR = 1.3 and similar irradiance. The reduced photosynthetic capacity under R:FR = 0.7 and high irradiance. In natural environments, leaves may experience low R:FR conditions temporarily during their development, and this may affect their future photosynthetic capacity in full sunlight.     

Effect of CO2-enrichnient on seedling physiology and growth of two tropical tree species

Seedlings of two tree species from the Atlantic lowlands of Costa Rica, Ochroma la-gopus Swartz, a fast-growing pioneer species, and Pentaclethra macroloba (Willd.) Kuntze, a slower-growing climax species, were grown under enriched atmospheric CO₂ in controlled environment chambers. Carbon dioxide concentrations were maintained at 350 and 675 μl 1⁻¹ under photosynthetic photon flux densities of 500 μol m⁻² s⁻¹ and temperatures of 26°C day and 20°C night. Total biomass of both species increased significantly in the elevated CO₂ treatment; the increase in biomass was greatest for the pioneer species, O. lagopus . Both species had greater leaf areas and specific leaf weights with increased atmospheric CO₂. However, the ratio of non-pho-tosynthetic tissue to leaf area also increased in both species leading to decreased leaf area ratios. Plants of both species grown at 675 μl 1⁻¹ CO₂ had lower chlorophyll contents and photosynthesis on a leaf area basis than those grown at 350 μl 1⁻¹. Reductions in net photosynthesis occurred despite increased internal CO₂ concentrations in the CO₂-enriched treatment. Stomatal conductances of both species decreased with CO₂-enrichment resulting in significant increases in water use efficiency.     

Interaction between sublethal pollution by sulphur dioxide and drought stress. The effect on photosynthetic capacity

Five-year-old Picea abies L. plants were grown in growth cabinets in the presence (3.1 μmol m⁻³) or absence of SO₂. After 5 weeks, the photosynthetic capacity of mature needles produced in the year was the same in both conditions. Trees were then submitted in situ to drought stress by withholding water. The decline of leaf photosynthetic capacity was greatest in the presence of SO₂. Chlorophyll decreased only when trees were submitted to dehydration in the presence of SO₂; however, this al-one could not account for the large decline in photosynthetic capacity observed under that condition. Needle water content was the lowest during dehydration in the presence of SO₂. It is concluded that the critical factor in the interaction between pollution by SO₂ and drought stress is the greater dehydration of the tissue found in stressed plants grown in the presence of SO₂. The large decline in photosynthetic capacity under such conditions might be due to this greater dehydration.     

Keeping a positive carbon balance under adverse conditions: responses of photosynthesis and respiration to water stress

Drought and salinity (i.e. soil water stress) are the main environmental factors limiting photosynthesis and respiration and, consequently, plant growth. This review summarizes the current status of knowledge on photosynthesis and respiration under water stress. It is shown that diffusion limitations to photosynthesis under most water stress conditions are predominant, involving decreased mesophyll conductance to CO₂, an important but often neglected process. A general failure of photochemistry and biochemistry, by contrast, can occur only when daily maximum stomatal conductance ( g _s) drops below 0.05–0.10 mol H₂O m⁻² s⁻¹. Because these changes are preceded by increased leaf antioxidant activities ( g _s below 0.15–0.20 mol H₂O m⁻² s⁻¹), it is suggested that metabolic responses to severe drought occur indirectly as a consequence of oxidative stress, rather than as a direct response to water shortage. As for respiration, it is remarkable that the electron partitioning towards the alternative respiration pathway sharply increases at the same g _s threshold, although total respiration rates are less affected. Despite the considerable improvement in the understanding of plant responses to drought, several gaps of knowledge are highlighted which should become research priorities for the near future. These include how respiration and photosynthesis interact at severe stress, what are the boundaries and mechanisms of photosynthetic acclimation to water stress and what are the factors leading to different rates of recovery after a stress period.