Impairment of photosynthesis by chilling-temperatures in tomato

Chilling of attached tomato leaves (cv. Rutgers) in the dark for 16 hours at 1 C decreased both photosynthesis and transpiration. To separate the effects of chilling on stomatal CO₂ conductance from more direct effects of chilling on the chloroplasts' activities, measurements of photosynthesis and transpiration were made at atmospheric and saturating CO₂ levels. At atmospheric CO₂, the inhibition of photosynthesis was approximately 60%, of which about 35% was attributable to the impairment of chloroplast function and about 25% was attributable to decreased stomatal conductance. However, the affinity of the photosynthetic apparatus for CO₂ was not changed by chilling, since the dependence of the relative rate of photosynthesis on the intercellular CO₂ concentration was unaltered. The apparent quantum requirement for CO₂ reduction also was identical in chilled and unchilled plants. This observation contradicts the widely held notion that the chilling-induced inhibition of photosynthesis is caused by an impairment of the water oxidation mechanism. The impairment of chloroplast activity was not a consequence of an unfavorable water status within the leaf, since chilling caused only a small drop (1 bar) in water potential. A small loss of chlorophyll resulted as a secondary effect of chilling, but this loss of chlorophyll was eliminated as a cause of the inhibition of photosynthesis.     

Analysis of the gas exchange components in chilled tomato plants

A positive linear relationship between the net CO₂ exchange rate (P _N) and the leaf stomatal conductance (g_s) under an optimal temperature, and even more distinct one after a short-term chilling (CH, 15-17 h, 2 °C in darkness), that was found in two tomato cultivars (sensitive to a low temperature cv. Robin and tolerant cv. New Yorker) suggested a partial stomatal limitation of photosynthesis. The CH treatment of cv. Robin resulted in an intercellular CO₂ concentration (C _i) increase because of which a negative correlation between C _i and P _N was observed. In cv. New Yorker a positive correlation was observed. Detrimental effect of the low temperature in cv. Robin was more evident in plants with a relatively small root system (SR), but drought-hardening positively affected the response to CH only in the plants with bigger roots (BR). On the contrary, in cv. New Yorker the favourable effect of such pre-treatment was more evident in SR than in BR plants. This revised version was published online in June 2006 with corrections to the Cover Date.     

Effects of Abscisic Acid Application on Photosynthesis and Photochemistry of Stylosanthes guianensis under Chilling Stress

In our previous study, it was found that abscisic acid (ABA) improved the chilling resistance of Stylosanthes guianensis. In order to determine the effects of ABA on photosynthesis and photochemistry of S. guianensis, an experiment was conducted under controlled condition to determine the effects of exogenous ABA on stomatal conductance (g_s), transpiration (E), photosynthetic rate (A) and chlorophyll a fluorescence of this pasture legume. The results showed that ABA treatment reduced A, g_s, and E under both chilling (8 °C) and control temperature (28 °C). A of the ABA treated plants returned to a high rate, while that of the water-treated plants remained low when plants were rewarmed after chilling treatment. ABA-treated plants had higher maximum photochemical efficiency (F_v/F_m), non-photochemical quenching (NPQ), quantum efficiency of PS II photochemistry (Φ_{ps ii}) than water-treated ones during chilling. Although the biomass of S. guianensis was reduced by ABA under control temperature, ABA-treated plants had higher biomass than water-treated ones after 7 days of recovery.     

Piriformospora indica inoculation alleviates the adverse effect of NaCl stress on growth,gas exchange and chlorophyll fluorescence in tomato (Solanum lycopersicum L.)

• Salinity is now an increasingly serious environmental issue that affects the growth and yield of many plants.
• In the present work, the influence of inoculation with the symbiotic fungus, Piriformospora indica, on gas exchange, water potential, osmolyte content, Na/K ratio and chlorophyll fluorescence of tomato plants under three salinity levels (0, 50, 100 and 150 mm NaCl) and three time periods (5, 10 and 15 days after exposure to salt) was investigated.
• Results indicate that P. indica inoculation improved growth parameters of tomato under salinity stress. This symbiotic fungus significantly increased photosynthetic pigment content under salinity, and more proline and glycine betaine accumulated in inoculated roots than in non‐inoculated roots. P. indica further significantly improved K⁺ content and reduced Na⁺ level under salinity treatment. After inoculation with the endophytic fungus, leaf physiological parameters, such as water potential, net photosynthesis, stomatal conductance and transpiration, were all higher under the salt concentrations and durations compared with controls without P. indica. With increasing salt level and salt treatment duration, values of F₀ and qP increased but F_m, F_v/F_m, F′_v/F′_m and NPQ declined in the controls, while inoculation with P. indica improved these values.
• The results indicate that the negative effects of NaCl on tomato plants were alleviated after P. indica inoculation, probably by improving physiological parameters such as water status and photosynthesis.

     

Chill-induced inhibition of photosynthesis was alleviated by 24-epibrassinolide pretreatment in cucumber during chilling and subsequent recovery

To investigate whether brassinosteroids (BRs) could be used to alleviate chill-induced inhibition of photosynthesis in cucumber (Cucumis sativus L) during chilling and subsequent recovery, the effects of exogenously applied 24-epibrassinolide (EBR) on gas exchange, chlorophyll fluorescence parameters, and antioxidant enzyme activity were studied. Cucumber plants were exposed to chilling under low light (12/8°C and 100 μmol m⁻² s⁻¹ PPFD) for 3 days and then recovered under normal temperature and high irradiance (28/18°C and 600 μmol m⁻² s⁻¹ PPFD) for 6 days. Chilling significantly decreased the net photosynthetic rate (P _N) and stomatal conductance (g _s), and increased rate of O₂ ^·− formation and H₂O₂ and malondialdehyde (MDA) content in cucumber leaves, but did not influence the optimal quantum yield of PSII (F_v/F_m). Chilling also decreased the effective quantum yield of PSII photochemistry (Φ_PSII) and photochemical quenching (q_P), but induced an increase in nonphotochemical quenching (NPQ), and the activities of superoxide dismutase (SOD) and ascorbate peroxidase (APX). High irradiance (600 μmol m⁻² s⁻¹) further aggravated the decrease in P _N, g _s, Φ_PSII and q_P, and enhanced the increase in reactive oxygen species (ROS) generation and accumulation in the first day of recovery after chilling. However, high irradiance induced a sharp decrease in F_v/F_m and NPQ, as well as the activities of SOD and APX on the first day of recovery. EBR pretreatment significantly alleviated chill-induced inhibition of photosynthesis during chilling stress and subsequent recovery period, which was mainly due to significant increases in g _s, Φ_PSII, q_P and NPQ. EBR pretreatment also reduced ROS generation and accumulation, and increased the activities of SOD and APX during chilling and subsequent recovery. Those results suggest that EBR pretreatment alleviates the chill reduction in photosynthesis and accelerated the recovery rate mainly by increasing of the stomatal conductance, the efficiency of utilization and dissipation of leaf absorbed light, and the activity of the ROS scavenging system during chilling and subsequent recovery period.     

The recovery of photosynthesis in tomato subsequent to chilling exposure

The overall success of a plant in coping with low temperature sensitivity of photosynthesis is dependent not only on the maximum extent of inhibition suffered for a given time of low temperature exposure but also on the persistence of the inhibition after normal growth temperatures are restored. Thus the capacity of recovery and the speed with which a plant can recover from the effects of chilling exposure are important parameters in determining how devastating the chilling event will be on season-long growth and yields. We have studied the recovery of CO₂-saturated photosynthesis from the injury caused by exposing intact tomato plants (Lycopersicon esculentum Mill. cv. Floramerica) or detached tomato leaves to a temperature of 1°C in the dark for varying periods of time. We found that net photosynthesis was fully recovered within 12 h after returning the plants to 25°C in the dark, even after chilling exposures as long as 45 h. This was true for intact plants as well as for detached leaves that were supplied with water. When chilling took place in the light (4°C, 1000 E · m^-2 · s^-1, PAR) inhibition of photosynthesis was more severe and appeared more quickly and the recovery was slower and incomplete. A 12 h chilling exposure in the light resulted in injury to net photosynthesis that was not fully recovered even after 50 h. Chilling damage to photosynthesis developing in the light was distinguished from chilling in the dark by the decreased photosynthetic quantum yield. Not only did high intensity illumination enhance chilling damage of photosynthesis but bright light subsequent to the chilling exposure also delayed the recovery of photosynthesis. At none of the three ambient CO₂ concentrations investigated (300, 1500 and 5000 1.1^-1) did the recovery of photosynthesis depend on stomatal conductance.     

Antisense-mediated suppression of tomato zeaxanthin epoxidase alleviates photoinhibition of PSII and PSI during chilling stress under low irradiance

A tomato (Lycopersicon esculentum Mill.) zeaxanthin epoxidase gene (LeZE) was isolated and antisense transgenic tomato plants were produced. Northern, southern, and western blot analyses demonstrated that antisense LeZE was transferred into the tomato genome and the expression of LeZE was inhibited. The ratio of (A+Z)/(V+A+Z) in antisense transgenic plants was maintained at a higher level than in the wild type (WT) plants under high light and chilling stress with low irradiance. The value of non-photochemical quenching (NPQ) in WT and transgenic plants was not affected during the stresses. The oxidizable P700 and the maximal photochemical efficiency of PSII (F_v/F_m) in transgenic plants decreased more slowly at chilling temperature under low irradiance. These results suggested that suppression of LeZE caused zeaxanthin accumulation, which was helpful in alleviating photoinhibition of PSI and PSII in tomato plants under chilling stress.     

Analysis of the gas exchange components in chilled tomato plants

A positive linear relationship between the net CO₂ exchange rate (P _N) and the leaf stomatal conductance (g_s) under an optimal temperature, and even more distinct one after a short-term chilling (CH, 15-17 h, 2 °C in darkness), that was found in two tomato cultivars (sensitive to a low temperature cv. Robin and tolerant cv. New Yorker) suggested a partial stomatal limitation of photosynthesis. The CH treatment of cv. Robin resulted in an intercellular CO₂ concentration (C _i) increase because of which a negative correlation between C _i and P _N was observed. In cv. New Yorker a positive correlation was observed. Detrimental effect of the low temperature in cv. Robin was more evident in plants with a relatively small root system (SR), but drought-hardening positively affected the response to CH only in the plants with bigger roots (BR). On the contrary, in cv. New Yorker the favourable effect of such pre-treatment was more evident in SR than in BR plants.     

The influence of chilling on photosynthesis and activities of some enzymes of sucrose metabolism in Lycopersicon esculentum Mill

The effects of chilling stress on leaf photosynthesis and sucrose metabolism were investigated in tomato plants (Lycopersicon esculentum Mill. cultivar Marmande). Twenty-one-day-old seedlings were grown in a growth chamber at 25/23 °C (day/night) (control) and at 10/8 °C (day/night) (chilled) for 7 days. The most evident effect of chilling was the marked reduction of plant growth and of CO₂ assimilation as measured after 7 days, the latter being associated with a decrease in stomatal closure and an increase in Ci. The inhibition in photosynthetic rate was also related to an impairment of photochemistry of photosystem II (PSII), as seen from the slight, but significant change in the ratio of F_v/F_m. The capacity of chilled leaves to maintain higher q_P values with respect to the controls suggests that some protection mechanism prevented excess reduction of PSII acceptors. The results of the determination of starch and soluble sugar content could show that chilling impaired sucrose translocation. The activity of leaf invertase increased significantly in chilled plants, while that of other sucrose-metabolizing enzymes was not affected by growing temperature. Furthermore, the increase in invertase (neutral and acid) activity, which is typical of senescent tissue characterized by reduced growth, seems to confirm that tomato is a plant which is not a plant genetically adapted to low temperatures.     

Guard cell photosynthesis is critical for stomatal turgor production,yet does not directly mediate CO2‐ and ABA‐induced stomatal closing

Stomata mediate gas exchange between the inter‐cellular spaces of leaves and the atmosphere. CO₂ levels in leaves (Ci) are determined by respiration, photosynthesis, stomatal conductance and atmospheric [CO₂]. [CO₂] in leaves mediates stomatal movements. The role of guard cell photosynthesis in stomatal conductance responses is a matter of debate, and genetic approaches are needed. We have generated transgenic Arabidopsis plants that are chlorophyll‐deficient in guard cells only, expressing a constitutively active chlorophyllase in a guard cell specific enhancer trap line. Our data show that more than 90% of guard cells were chlorophyll‐deficient. Interestingly, approximately 45% of stomata had an unusual, previously not‐described, morphology of thin‐shaped chlorophyll‐less stomata. Nevertheless, stomatal size, stomatal index, plant morphology, and whole‐leaf photosynthetic parameters (PSII, qP, qN, F_V′/F_M′) were comparable with wild‐type plants. Time‐resolved intact leaf gas‐exchange analyses showed a reduction in stomatal conductance and CO₂‐assimilation rates of the transgenic plants. Normalization of CO₂ responses showed that stomata of transgenic plants respond to [CO₂] shifts. Detailed stomatal aperture measurements of normal kidney‐shaped stomata, which lack chlorophyll, showed stomatal closing responses to [CO₂] elevation and abscisic acid (ABA), while thin‐shaped stomata were continuously closed. Our present findings show that stomatal movement responses to [CO₂] and ABA are functional in guard cells that lack chlorophyll. These data suggest that guard cell CO₂ and ABA signal transduction are not directly modulated by guard cell photosynthesis/electron transport. Moreover, the finding that chlorophyll‐less stomata cause a ‘deflated’ thin‐shaped phenotype, suggests that photosynthesis in guard cells is critical for energization and guard cell turgor production.     

PHOTOSYNTHETIC FUNCTION IN DUNALIELLA TERTIOLECTA (CHLOROPHYTA) DURING A NITROGEN STARVATION AND RECOVERY CYCLE

Phytoplankton can be exposed to periods of N starvation with episodic N resupply. N starvation in Dunaliella tertiolecta (Butcher) measured over 4 days was characterized by slow reduction in cell chl and protein content and chl/carotenoid ratio and a decline in photosynthetic capacity and maximum quantum yield of photosynthesis (F_v/F_m). In the early stages of N starvation, cell division was maintained despite reduction in cellular chl. Chl content was more sensitive than carotenoids to N deprivation, and cellular chl a was maintained preferentially over chl b under N starvation. NO₃^? resupply stimulated rapid and complete recovery of F_v/F_m (from 0.4 to 0.7) within 24 h and commencement of cell division after 10 h, although N‐replete levels of cell chl and protein were not reestablished within 24 h. Recovery of F_v/F_m was correlated with increases in cell chl and protein and was more related to increases in F_m than to changes in F₀. Recovery of F_v/F_m was biphasic with a second phase of recovery commencing 4–6 h after resupply of NO₃^?. Uptake of NO₃^? from the external medium and the recovery of F_v/F_m, cell chl, and protein were inhibited when either cytosolic or chloroplastic protein synthesis was inhibited by cycloheximide or lincomycin, respectively; a time lag observed before maximum NO₃^? uptake was consistent with synthesis of NO₃^? transporters and assimilation enzymes. When both chloroplastic and cytosolic translation was inhibited, F_v/F_m declined dramatically. Dunaliella tertiolecta demonstrated a capacity to rapidly reestablish photosynthetic function and initiate cell division after N resupply, an important strategy in competing for limiting inorganic N resources.     

Recovery responses of photosynthesis,transpiration, and stomatal conductance in kidney bean following drought stress

Photosynthesis, transpiration, stomatal conductance and chlorophyll fluorescence characteristics were examined in kidney bean plants, with developing gradually water stress for several days after watering and then permitted to recover by re-watering. The photosynthetic rate, transpiration rate, and stomatal conductance decreased rapidly by withholding water for 2 days. The F_v/F_m of chlorophyll fluorescence characteristics slightly decreased when the water was withheld for 7 days. After re-watering the rate of recovery of photosynthesis, transpiration, and stomatal conductance decreased gradually as the days without watering became longer. The differences existed in rates of recovery of photosynthesis, transpiration, and stomatal conductance following drought stress. Among the fractional recoveries the highest was photosynthesis, and the lowest was stomatal conductance. Photosynthesis rate following drought stress was rapidly recovered until 2 days after re-watering, then recovered slowly. The critical time for the recovery of photosynthesis was recognized. The results show clearly a close correlation between the leaf water potential and the recovery level and speed of photosynthesis, transpiration, and stomatal conductance.     

Water relations under root chilling in a sensitive and tolerant tomato species

The shoots of cultivated tomato (Lycopersicon esculentum cv. T5) wilt if their roots are exposed to chilling temperatures of around 5 °C. Under the same treatment, a chilling‐tolerant congener (Lycopersicon hirsutum LA 1778) maintains shoot turgor. To determine the physiological basis of this differential response, the effect of chilling on both excised roots and roots of intact plants in pressure chambers were investigated. In excised roots and intact plants, root hydraulic conductance declined with temperature to nearly twice the extent expected from the temperature dependence of the viscosity of water, but the response was similar in both species. The species differed markedly, however, in stomatal behaviour: in L. hirsutum, stomatal conductance declined as root temperatures were lowered, whereas the stomata of L. esculentum remained open until the roots reached 5 °C, and the plants became flaccid and suffered damage. Grafted plants with the shoots of one genotype and roots of another indicated that the differential stomatal behaviour during root chilling has distinct shoot and root components.     

Influence of Manganese Toxicity on Photosynthesis in Ricebean (Vigna Umbellata) Seedlings

Influence of manganese (Mn) toxicity on photosynthesis in ricebean (Vigna umbellata) was studied by the measurement of gas exchange characteristics and chlorophyll fluorescence parameters. The net photosynthetic rate (P _N), transpiration rate (E), and stomatal conductance (g _s) were reduced with increasing Mn concentration in nutrient solution. The reduction in g _s and E was more pronounced at 6 d of Mn treatment. However, P _N declined at 2 d of Mn treatment implying that the reduction in photosynthesis was not due to the direct effect of Mn on stomatal regulation. Mn did not affect the maximum efficiency of photosystem 2 (PS2) photochemistry (F_v/F_m). A reduction in photochemical quenching (q_P) and excitation capture efficiency of open PS2 (F_v′/F_m′) with a concomitant increase in q_N was observed. This implies that reduced demand for ATP and NADPH due to the reduction in photosynthesis causes a down-regulation of PS2 photochemistry and thus a high pH gradient (increase in q_N) and limited electron transport (decreased q_P). This revised version was published online in August 2006 with corrections to the Cover Date.     

Photosynthetic responses of Populus przewalski subjected to drought stress

Cuttings of P. przewalski were exposed to two different watering regimes which were watered to 100 and 25 % of field capacity (WW and WS, respectively). Drought stress not only significantly decreased net photosynthetic rate (P _N), transpiration rate (E), stomatal conductance (g _s), efficiency of photosystem 2 (PS2) (F_v/F_m and yield), and increased intrinsic water use efficiency (WUE_i) under controlled optimal conditions, but also altered the diurnal changes of gas exchange, chlorophyll fluorescence, and WUE_i. On the other hand, WS also affected the P _N-photosynthetically active radiation (PAR) response curve. Under drought stress, P _N peak appeared earlier (at about 10:30 of local time) than under WW condition (at about 12:30). At midday, there was a depression in P _N for WS plants, but not for WW plants, and it could be caused by the whole microclimate, especially high temperature, low relative humidity, and high PAR. There were stomatal and non-stomatal limitations to photosynthesis. Stomatal limitation dominated in the morning, and low P _N at midday was caused by both stomatal and non-stomatal limitations, whereas non-stomatal limitation dominated in the afternoon. In addition, drought stress also increased compensation irradiance and dark respiration rate, and decreased saturation irradiance and maximum net photosynthetic rate. Thus drought stress decreased plant assimilation and increased dissimilation through affected gas exchange, the diurnal pattern of gas exchange, and photosynthesis-PAR response curve, thereby reducing plant growth and productivity.     

Developing a mathematical model for variation of physiological responses of Jatropha curcas leaves depending on leaf positions under soil flooding

The effect of soil flooding on photosynthesis, transpiration and stomatal conductance of Jatropha curcas seedlings were studied under natural environmental variables. Soil flooding reduced photosynthesis (P _N), transpiration (E) and stomatal conductance (gs) in response to leaf positions of Jatropha curcas plants. Based on the results, we conclude that decrease in stomatal opening and stomatal limitation of photosynthesis, followed by decrease in individual leaf area are the main causes of reductions in carbon uptake of flooded seedlings. A mathematical relationship was successfully developed to describe photosynthesis, transpiration and stomatal response of Jatropha under soil flooding stress.     

Response of xanthophyll cycle and chloroplastic antioxidant enzymes to chilling stress in tomato over-expressing glycerol-3-phosphate acyltransferase gene

Over-expression of chloroplastic glycerol-3-phosphate acyltransferase gene (LeGPAT) increased unsaturated fatty acid contents in phosphatidylglycerol (PG) of thylakoid membrane in tomato. The effect of this increase on the xanthophyll cycle and chloroplast antioxidant enzymes was examined by comparing wild type (WT) tomato with the transgenic (TG) lines at chilling temperature (4 °C) under low irradiance (100 μmol m⁻² s⁻¹). Net photosynthetic rate and the maximal photochemical efficiency of photosystem (PS) 2 (F_v/F_m) in TG plants decreased more slowly during chilling stress and F_v/F_m recovered faster than that in WT plants under optimal conditions. The oxidizable P700 in both WT and TG plants decreased during chilling stress under low irradiance, but recovered faster in TG plants than in the WT ones. During chilling stress, non-photochemical quenching (NPQ) and the de-epoxidized ratio of xanthophyll cycle in WT plants were lower than those of TG tomatoes. The higher activities of superoxide dismutase (SOD) and ascorbate peroxidase (APX) in TG plants resulted in the reduction of O₂ ^−· and H₂O₂ contents during chilling stress. Hence the increase in content of unsaturated fatty acids in PG by the over-expression of LeGPAT could alleviate photoinhibition of PS2 and PS1 by improving the de-epoxidized ratio of xanthophyll cycle and activities of SOD and APX in chloroplast.     

Diurnal Changes of Gas Exchange,Chlorophyll Fluorescence,and Stomatal Aperture of Hybrid Poplar Clones Subjected to Midday Light Stress

Diurnal changes in net photosynthetic rate (P _N), chlorophyll (Chl) fluorescence, and stomatal aperture of several hybrid poplar clones subjected to midday light stress were measured in July and August of 1996. Midday depression of P _N, photosystem 2 (PS2) efficiency, stomatal conductance (g _s), and stomatal aperture was observed in all clones, though at differing rates among them. Non-uniform stomatal closure occurred at noon and at other times, requiring a modification of intercellular CO₂ concentration (C ₁). A linear relationship was found between g _s and stomatal aperture. More than half of the photons absorbed by PS2 centre dissipated thermally when subjected to light stress at noon. There was a linear relationship between the rate of PS2 photochemical electron transport (PxPFD) and P _N. There was a consensus for two fluorescence indicators (1 – q_P/q_N and (F_m' – F)/F_m') in assessment of susceptibility of photoinhibition in the clones. According to P _N, Chl fluorescence, and stomatal aperture, we conclude that midday depression of photosynthesis can be attributed to both stomatal and non-stomatal limitations.     

Effects of exogenous glycinebetaine on growth, CO2 assimilation, and photosystem II photochemistry of maize plants

Effects of exogenous glycinebetaine (GB, 2–50 mM) on growth, photosynthetic gas exchange, PSII photochemistry, and the activities of key enzymes involved in CO₂ fixation in maize plants were investigated. Growth, CO₂ assimilation rate, and stomatal conductance increased at low GB concentrations (2–20 mM) but decreased significantly at high GB concentrations (30–50 mM). Leaf relative water content and water potential remained unchanged at low GB concentrations but decreased at high GB concentrations. The maximal efficiency of PSII photochemistry was unchanged either at low or high GB concentrations. The actual PSII efficiency ( Φ _PSII) and photochemical quenching (q_P) increased at low GB concentrations but decreased at high GB concentrations. At low GB concentrations, there were no significant changes in the efficiency of excitation energy capture by open PSII reaction centres (F_v′/F_m′) and non‐photochemical quenching (q_N). At high GB concentrations, F_v′/F_m′ decreased while q_N increased significantly. There were no changes in the activities of phosphoenolpyruvate carboxylase, pyruvate phosphate dikinase, and ribulose‐1,5‐bisphosphate carboxylase in control and GB‐fed plants. However, there was a linear correlation between CO₂ assimilation rate and stomatal conductance in control and GB‐fed plants. Moreover, there were no significant differences in O₂ evolution rate between control and GB fed‐plants under saturated CO₂ conditions. The results suggest that exogenous GB application at certain concentrations can enhance CO₂ assimilation rate, which can be explained by an increased stomatal conductance.     

Low humidity effects on photosynthesis in single leaves of C4 plants

Summary It was hypothesized that since sub-stomatal carbon dioxide concentrations are often saturating to photosynthesis at ambient external concentrations in C₄ plants at high light, photosynthesis might be insensitive to partial stomatal closure caused by large leaf-air water vapor pressure difference. The response of stomatal conductance and photosynthesis at high irradiance to vapor pressure difference was determined under uniform conditions in C₄ plants grown under controlled conditions, and outdoors. In several cases, photosynthesis was less sensitive to stomatal closure than it would have been if photosynthesis had a linear response to sub-stomatal carbon dioxide concentration. No change in photosynthesis at up to 25 mbar vapor pressure difference was demonstrated in the C₄ species Portulaca oleracea and Amaranthus hypochondriacus, despite reductions in stomatal conductance of 32 and 17%, respectively. Sensitivity of photosynthesis to leaf-air vapor pressure difference was found to depend on the species and on the growth conditions.