Dynamics of patchy stomatal movements, and their contribution to steady-state and oscillating stomatal conductance calculated using gas-exchange techniques

Patchy stomatal movements were induced in leaves of Helianthus annuus L. and Xanthium strumarium L. by increasing Δw and decreasing light in a gas-exchange cuvette. The dynamics of the patchy movements were recorded and analysed using images of chlorophyll fluorescence, and the influence of heterogeneous stomatal activity on gas-exchange measurements of whole-leaf stomatal conductance was explored. Image series and gas-exchange measurements from two contrasting 100 min experiments are presented. One series of images, taken using Helianthus annuus, was characterized by strongly oscillating stomatal conductance induced by a decrease in light at high Δw. Fluorescence analysis revealed that individual patches of the leaf displayed a variety of behaviours (from static to strongly oscillating fluorescence), which, when averaged, matched the time dependence of the oscillating stomatal conductance measured by gas-exchange techniques. During the second series of images, taken using Xanthium strumarium, stomatal conductance (measured with gas exchange) declined slightly after an increase in Δw, and then maintained a steady state. Again, some patches in this leaf showed highly dynamic q_NP, although on the whole q_NP varied without any obvious pattern or frequency. When all patch activity in this series was averaged, it paralleled the steady whole-leaf stomatal conductance determined by gas-exchange measurements. It is clear from this work that coordinated patchy stomatal movements can contribute significantly to the dynamics of whole-leaf stomatal conductance, and, in contrast, that dynamic but uncoordinated patchy movements can average to produce a steady gas-exchange trace.     

Jasmonic acid and salicylic acid play minor roles in stomatal regulation by CO2, abscisic acid,darkness, vapor pressure deficit and ozone

Jasmonic acid (JA) and salicylic acid (SA) regulate stomatal closure, preventing pathogen invasion into plants. However, to what extent abscisic acid (ABA), SA and JA interact, and what the roles of SA and JA are in stomatal responses to environmental cues, remains unclear. Here, by using intact plant gas-exchange measurements in JA and SA single and double mutants, we show that stomatal responsiveness to CO₂, light intensity, ABA, high vapor pressure deficit and ozone either did not or, for some stimuli only, very slightly depended upon JA and SA biosynthesis and signaling mutants, including dde2, sid2, coi1, jai1, myc2 and npr1 alleles. Although the stomata in the mutants studied clearly responded to ABA, CO₂, light and ozone, ABA-triggered stomatal closure in npr1-1 was slightly accelerated compared with the wild type. Stomatal reopening after ozone pulses was quicker in the coi1-16 mutant than in the wild type. In intact Arabidopsis plants, spraying with methyl-JA led to only a modest reduction in stomatal conductance 80 min after treatment, whereas ABA and CO₂ induced pronounced stomatal closure within minutes. We could not document a reduction of stomatal conductance after spraying with SA. Coronatine-induced stomatal opening was initiated slowly after 1.5–2.0 h, and reached a maximum by 3 h after spraying intact plants. Our results suggest that ABA, CO₂ and light are major regulators of rapid guard cell signaling, whereas JA and SA could play only minor roles in the whole-plant stomatal response to environmental cues in Arabidopsis and Solanum lycopersicum (tomato).     

Stomatal and non-stomatal limitations to carbon assimilation: an evaluation of the path-dependent method

Abstract Environmental stresses can decrease photosynthesis by a direct effect on photosynthetic capacity of the mesophyll or by a CO₂ limitation resulting from stomatal closure. In the present study, a ‘path-dependent method’ (Jones, 1985) for the partitioning of a stress-related decline in assimilation rate between non-stomatal and stomatal factors was evaluated, using light quality as a ‘stress’. Kinetic data on assimilation rate and conductance of Phragmipedium longifolium following a change in light quality from 95 μmol m^?2s^?1 white light to 95 μmol m^?2s^?1 red light failed to generate a smooth response curve for conductance. Partitioning of limitations on assimilation by a path-dependent method that utilizes the actual trajectories of conductance and assimilation was therefore not feasible. A simplified path-dependent method (Jones, 1985) which assumes that either mesophyll cells or guard cells respond first to a stress was applied to steady-state measurements of assimilation and conductance under red and white illumination. Either 5% or 23% of the observed reduction in assimilation rate under white light was attributable to stomatal factors, depending on whether the ‘stomatal first’ or the ‘mesophyll first’ path was assumed. In the absence of additional information indicating the appropriate choice of path, arbitrary choice may therefore lead to widely divergent estimates, and potentially erroneous conclusions. An alternative approach to the evaluation of the importance to carbon assimilation of stomatal and non-stomatal factors is suggested.     

Stomatal versus biochemical limitations to dynamic photosynthetic performance in four tropical rainforest shrub species

Photosynthetic performance under dynamic light regimes was assessed in four different species of tropical shrubs from the family Rubiaceae via field gas exchange measurements conducted on Barro Colorado Island, Panamá. Rates of photosynthetic induction and induction loss were assessed throughout the day in both the wet and dry seasons in order to determine the relative roles of stomata and biochemistry in limiting photosynthetic performance under transient light conditions. A high degree of coordination was observed between stomatal conductance and biochemical capacity for CO₂ assimilation during induction. Rates of biochemical and overall photosynthetic induction sharply decreased when initial stomatal conductance fell below a narrow range of critical values. Time of day or season did not affect rates of biochemical deactivation upon shading, but did influence stomatal closure, which often exerted a significant influence over induction loss in the darkness. In measurements of total assimilation due to a 60-s light pulse, both biochemical activity and stomatal conductance were linearly related to total CO₂ uptake. Only during the mornings of the wet season was stomatal conductance consistently high enough to be non-limiting to dynamic photosynthetic performance. At all other times, stomatal behavior exercised significant influence over induction times, photosynthetic induction loss, and total CO₂ uptake from 60-s light pulses. Received: 17 March 1999 / Accepted: 26 October 1999     

Model-based analysis of avoidance of ozone stress by stomatal closure in Siebold's beech (Fagus crenata)

Background and Aims

Resistance of plants to ozone stress can be classified as either avoidance or tolerance. Avoidance of ozone stress may be explained by decreased stomatal conductance during ozone exposure because stomata are the principal interface for entry of ozone into plants. In this study, a coupled photosynthesis–stomatal model was modified to test whether the presence of ozone can induce avoidance of ozone stress by stomatal closure.

Methods

The response of Siebold''s beech (Fagus crenata), a representative deciduous tree species, to ozone was studied in a free-air ozone exposure experiment in Japan. Photosynthesis and stomatal conductance were measured under ambient and elevated ozone. An optimization model of stomata involving water, CO₂ and ozone flux was tested using the leaf gas exchange data.

Key Results

The data suggest that there are two phases in the avoidance of ozone stress via stomatal closure for Siebold''s beech: (1) in early summer ozone influx is efficiently limited by a reduction in stomatal conductance, without any clear effect on photosynthetic capacity; and (2) in late summer and autumn the efficiency of ozone stress avoidance was decreased because the decrease in stomatal conductance was small and accompanied by an ozone-induced decline of photosynthetic capacity.

Conclusions

Ozone-induced stomatal closure in Siebold''s beech during early summer reduces ozone influx and allows the maximum photosynthetic capacity to be reached, but is not sufficient in older leaves to protect the photosynthetic system.     

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.     

干旱胁迫对降香黄檀幼苗光合生理特性的影响

采用温室盆栽方法,设置对照(CK)、轻度(LS)、中度(MS)和重度(HS)干旱胁迫4个水分条件,研究不同水分条件对降香黄檀幼苗光合和生理特性的影响。结果表明:(1)随着干旱胁迫程度增加,降香黄檀幼苗叶片叶绿素总含量总体呈现出下降趋势。(2)降香黄檀幼苗叶片净光合速率、气孔导度、胞间CO2浓度和蒸腾速率随着干旱胁迫强度增加均呈现出先增加后降低趋势,且MS和HS处理下的气孔导度和胞间CO2浓度同时降低,此时幼苗光合能力的下降主要受气孔因素限制。(3)随着干旱胁迫强度的增加,降香黄檀幼苗叶片细胞膜相对透性、丙二醛含量、游离脯氨酸含量和POD活性均呈现出增加趋势,而同期SOD和CAT活性呈现出先升高后降低趋势。可见,降香黄檀幼苗在轻度干旱胁迫下可通过增加叶片保护酶活性来清除活性氧对其组织造成的伤害,但胁迫超过一定程度后保护酶活性下降,表明降香黄檀幼苗的耐旱能力有限。     

Effect of canopy gap light environment on evaporative load and stomatal conductance in the temperate forest understory herb Aster macrophyllus (Asteraceae)

Aster macrophyllus, a temperate forest understory species of the northeastern United States, inhabits a broad range of light habitats. Plants receiving several minutes of direct sun in canopy gap and forest edge habitats occasionally wilt, a response indicative of water stress. We compared two alterative scenarios for patterns of evaporative load and stomatal conductance for plants in large (0.15 ha) tree canopy gaps and small (3 m²) herbaceous subcanopy gaps: 1) evaporative loads are typically moderate and stomatal conductance is largely governed by light intensity; or 2) evaporative loads are often substantial, mandating stomatal closure to prevent excessive transpiration. In all cases evaporative loads were elevated by light intensity above 25% of full sun. This was accompanied by substantial stomatal closure. Transitions from low to moderate light intensity (<13% full sun) caused little increase in leaf evaporative load, and stimulated increases in stomatal conductance. Very brief periods of high light also stimulated stomatal opening. Light environments in the small herbaceous subcanopy gaps differ greatly in their patterns of evaporative load from day to day.     

Increased stomatal conductance induces rapid changes to photosynthetic rate in response to naturally fluctuating light conditions in rice

A close correlation between stomatal conductance and the steady-state photosynthetic rate has been observed for diverse plant species under various environmental conditions. However, it remains unclear whether stomatal conductance is a major limiting factor for the photosynthetic rate under naturally fluctuating light conditions. We analysed a SLAC1 knockout rice line to examine the role of stomatal conductance in photosynthetic responses to fluctuating light. SLAC1 encodes a stomatal anion channel that regulates stomatal closure. Long exposures to weak light before treatments with strong light increased the photosynthetic induction time required for plants to reach a steady-state photosynthetic rate and also induced stomatal limitation of photosynthesis by restricting the diffusion of CO₂ into leaves. The slac1 mutant exhibited a significantly higher rate of stomatal opening after an increase in irradiance than wild-type plants, leading to a higher rate of photosynthetic induction. Under natural conditions, in which irradiance levels are highly variable, the stomata of the slac1 mutant remained open to ensure efficient photosynthetic reaction. These observations reveal that stomatal conductance is important for regulating photosynthesis in rice plants in the natural environment with fluctuating light.     

Photocontrol of the Functional Coupling between Photosynthesis and Stomatal Conductance in the Intact Leaf : Blue Light and Par-Dependent Photosystems in Guard Cells

The photocontrol of the functional coupling between photosynthesis and stomatal conductance in the leaf was investigated in gas exchange experiments using monochromatic light provided by lasers. Net photosynthesis and stomatal conductance were measured in attached leaves of Malva parviflora L. as a function of photon irradiance at 457.9 and 640.0 nanometers.

Photosynthetic rates and quantum yields of photosynthesis were higher under red light than under blue, on an absorbed or incident basis.

Stomatal conductance was higher under blue than under red light at all intensities. Based on a calculated apparent photon efficiency of conductance, blue and red light had similar effects on conductance at intensities higher than 0.02 millimoles per square meter per second, but blue light was several-fold more efficient at very low photon irradiances. Red light had no effect on conductance at photon irradiances below 0.02 millimoles per square meter per second. These observations support the hypothesis that stomatal conductance is modulated by two photosystems: a blue light-dependent one, driving stomatal opening at low light intensities and a photosynthetically active radiation (PAR)-dependent one operating at higher irradiances.

When low intensity blue light was used to illuminate a leaf already irradiated with high intensity, 640 nanometers light, the leaf exhibited substantial increases in stomatal conductance. Net photosynthesis changed only slightly. Additional far-red light increased net photosynthesis without affecting stomatal conductance. These observations indicate that under conditions where the PAR-dependent system is driven by high intensity red light, the blue light-dependent system has an additive effect on stomatal conductance.

The wavelength dependence of photosynthesis and stomatal conductance demonstrates that these processes are not obligatorily coupled and can be controlled by light, independent of prevailing levels of intercellular CO₂. The blue light-dependent system in the guard cells may function as a specific light sensor while the PAR-dependent system supplies a CO₂-modulated energy source providing functional coupling between the guard cells and the photosynthesizing mesophyll.

     

Water relations and hydraulic control of stomatal behaviour in bell pepper plant in partial soil drying

Two experiments, a split-root experiment and a root pressurizing experiment, were performed to test whether hydraulic signalling of soil drying plays a dominant role in controlling stomatal closure in herbaceous bell pepper plants. In the split-root experiment, when both root parts were dried, synchronous decreases in stomatal conductance (g_s), leaf water potential (LWP) and stem sap flow (SF_stem) were observed. The value of g_s was found to be closely related to soil water potential (SWP) in both compartments. Tight relationships were observed between g_s and stem sap flow under all conditions of water stress, indicating a complete stomatal adjustment of transpiration. When the half-root system has been dried to the extent that its water uptake dropped to almost zero, declines in g_s of less than 20% were observed without obvious changes in LWP. The reduced plant hydraulic conductance resulting from decreased sap flow and unchanged LWP may be a hydraulic signal controlling stomatal closure; the results of root pressurizing supported this hypothesis. Both LWP and g_s in water-stressed plants recovered completely within 25 min of the application of root pressurizing, and decreased significantly within 40 min after pressure release, indicating the hydraulic control of stomatal closure. Our results are in contrast to those of other studies on other herbaceous species, which suggested that chemical messengers from the roots bring about stomatal closure when plants are in water stress.     

Qualitative effects of patchy stomatal conductance distribution features on gas-exchange calculations

The qualitative influence of patchy stomatal conductance distributions on the values of photosynthesis (A) and intercellular CO₂ concentration (c_i) as determined by gas-exchange measurements were investigated using computer modelling. Gas-exchange measurements were simulated for different conductance distributions by modelling photosynthesis explicitly for each patch, summing these rates, and inferring c_i from a diffusion equation. Qualitative relationships are presented between conductance distribution features and the difference between assimilation rates measured for patchy and homogeneous leaves at the same c_i (A_p and A_h, respectively). These data show that, although most conductance distributions have little effect on the value of A measured for a given c_i, some distribution features (which we have termed ‘bimodality’, ‘position’, ‘skewness’ and ‘range’) play a key role in controlling the magnitude of these effects. Distributions that are more nearly bimodal, span regions of lower conductance, are right-skewed, or have broader conductance ranges are associated with larger effects on the A(c_i) relationship. To clarify our mathematical analysis and illustrate some of the trends it predicts, we present conductance distributions and gas-exchange data from leaves of Malus dolgo var. Spring Snow Dial were treated with ABA. The results are discussed in the light of recent controversy over the effect of patchy stomatal conductance on gas-exchange data.     

Neither xylem collapse,cavitation, or changing leaf conductance drive stomatal closure in wheat

Identifying the drivers of stomatal closure and leaf damage during stress in grasses is a critical prerequisite for understanding crop resilience. Here, we investigated whether changes in stomatal conductance (g_s) during dehydration were associated with changes in leaf hydraulic conductance (K_leaf), xylem cavitation, xylem collapse, and leaf cell turgor in wheat (Triticum aestivum). During soil dehydration, the decline of g_s was concomitant with declining K_leaf under mild water stress. This early decline of leaf hydraulic conductance was not driven by cavitation, as the first cavitation events in leaf and stem were detected well after K_leaf had declined. Xylem vessel deformation could only account for <5% of the observed decline in leaf hydraulic conductance during dehydration. Thus, we concluded that changes in the hydraulic conductance of tissues outside the xylem were responsible for the majority of K_leaf decline during leaf dehydration in wheat. However, the contribution of leaf resistance to whole plant resistance was less than other tissues (<35% of whole plant resistance), and this proportion remained constant as plants dehydrated, indicating that K_leaf decline during water stress was not a major driver of stomatal closure.     

Ozone‐induced stomatal sluggishness changes stomatal parameters of Jarvis‐type model in white birch and deciduous oak

• Stomatal ozone flux is closely related to ozone injury to plants. Jarvis‐type multiplicative model has been recommended for estimating stomatal ozone flux in forest trees. Ozone can change stomatal conductance by both stomatal closure and less efficient stomatal control (stomatal sluggishness). However, current Jarvis‐type models do not account for these ozone effects on stomatal conductance in forest trees.
• We examined seasonal course of stomatal conductance in two common deciduous tree species native to northern Japan (white birch: Betula platyphylla var. japonica ; deciduous oak: Quercus mongolica var. crispula ) grown under free‐air ozone exposure. We innovatively considered stomatal sluggishness in the Jarvis‐type model using a simple parameter, s , relating to cumulative ozone uptake (defined as POD : phytotoxic ozone dose).
• We found that ozone decreased stomatal conductance of white birch leaves after full expansion (?28%). However, such a reduction of stomatal conductance by ozone fell in late summer (?10%). At the same time, ozone reduced stomatal sensitivity of white birch to VPD and increased stomatal conductance under low light conditions. In contrast, in deciduous oak, ozone did not clearly change the model parameters.
• The consideration of both ozone‐induced stomatal closure and stomatal sluggishness improved the model performance to estimate stomatal conductance and to explain the dose–response relationship on ozone‐induced decline of photosynthesis of white birch. Our results indicate that ozone effects on stomatal conductance (i.e . stomatal closure and stomatal sluggishness) are crucial for modelling studies to determine stomatal response in deciduous trees, especially in species sensitive to ozone.

     

Short-chained oxygenated VOC emissions in <Emphasis Type="Italic">Pinus halepensis</Emphasis> in response to changes in water availability

Short-chained oxygenated VOC (oxVOCs) emissions from Pinus halepensis saplings were monitored in response to changes in water availability. Online measurements were made with a proton transfer reaction—mass spectrometer under controlled conditions, together with CO₂ and H₂O exchange measurements. Masses corresponding to methanol and acetone were the most emitted oxVOCs. All the oxVOC exchanges, except that of acetone (M59), were significantly related to stomatal conductance and transpiration. Acetaldehyde (M45) emission showed, moreover, a strong dependence on the concentration of acetaldehyde in the ambient: stomatal opening (stomatal conductance above 75 mmol m⁻² s⁻¹) only allowed increased emissions when external concentration were below 6 ppb. Acetone (M59) presented an important peak of emission following light and stomatal opening in the morning when plants were water stressed. Thus, the alterations in oxVOC emissions in P. halepensis caused by the water deficit seem to be mainly driven by water stress effect on stomatal closure and oxVOC air concentrations.     

Stomatal and nonstomatal limitations to net photosynthesis in seedlings of woody angiosperms

Comparative responses of net photosynthesis (A) to water stress in woody species from a variety of habitats were studied to assess the relationship between photosynthetic attributes and drought tolerance. Stomatal and nonstomatal limitations to A were compared in three-month-old white oak (Quercus alba L.), post oak (Quercus stellata Wangenh.), sugar maple (Acer saccharum Marsh.), and black walnut (Juglans nigra L.) seedlings during a drying cycle. Relative stomatal limitation of photosynthesis (I) was less than 50% in all species except for Q. stellata seedlings subjected to severe water stress. No significant changes in I were observed in Q. alba and J. nigra before, during, and after drought. In A. saccharum, I was generally low and decreased significantly under water stress. Under well-watered conditions, A was highest in Q. stellata, intermediate in Q. alba, and lower in A. saccharum and J. nigra. High A in well-watered Q. stellata was associated with high stomatal conductance and carboxylation efficiency, whereas low A was associated with low stomatal conductance and carboxylation efficiency in A. saccharum and low stomatal conductance, low carboxylation efficiency, and high CO₂ compensation point in J. nigra. Under severe water stress, A, carboxylation efficiency, and stomatal conductance decreased substantially in all species; however, Q. stellata had the highest carboxylation efficiency and lowest CO₂ compensation point under these conditions. After 5 days at high soil moisture after drought, stomatal and mesophyll components of A in A. saccharum and J. nigra had not recovered to predrought levels, whereas they had completely recovered in Q. stellata and Q. alba. The photosynthetic apparatus, especially mesophyll components, of drought-tolerant Quercus species showed either less inhibition under water stress, superior recovery to predrought capacity, or both. Exposure of the leaves to ¹⁴CO₂ indicated apparent asymmetric stomatal closure for mildly water-stressed seedlings, but not for leaves of well-watered, severely stressed, or rehydrated plants. These results suggest that patchy stomatal closure under mild water stress might be important for water stress-induced inhibition of photosynthesis, but not under the more severe water stress imposed in this study.     

Simulations and observations of patchy stomatal behavior in leaves of <Emphasis Type="Italic">Quercus crispula</Emphasis>, a cool-temperate deciduous broad-leaved tree species

We investigated the occurrence of patchy stomatal behavior in leaves of saplings and a forest canopy tree of Quercus crispula Blume. Through a combination of leaf gas-exchange measurements and numerical simulation, we detected patterns of stomatal closure (either uniform or patchy bimodal) coupled with depression of net assimilation rate (A). There was a clear inhibition of A associated with stomatal closure in leaves of Q. crispula during the day, but the magnitude of inhibition varied among days and growing conditions. Comparisons of observed and simulated A values for both saplings and the canopy tree identified patterns of stomatal behavior that shifted flexibly between uniform and patchy frequency distributions depending on environmental conditions. Bimodal stomatal closure explained severe depression of A in saplings under conditions of relatively high leaf temperature and vapor pressure deficit. Model simulations of A depression through bimodal stomatal closure were corroborated by direct observations of stomatal aperture distribution using Suzuki’s Micro-Printing method; these demonstrated that there was a real bimodal frequency distribution of stomatal apertures. Although there was a heterogeneous distribution of stomatal apertures both within and among patches, induction of heterogeneity in intercellular CO₂ concentration among patches, and hence severe depression of A, resulted only from bimodal stomatal closure among patches (rather than within patches).     

Gas-exchange characteristics,leaf water potential and chlorophyll <Emphasis Type="Italic">a</Emphasis> fluorescence in oil palm (<Emphasis Type="Italic">Elaeis guineensis</Emphasis> Jacq.) seedlings under water stress and recovery

The gas-exchange characteristics, leaf water potential and chlorophyll (Chl) a fluorescence of oil palm (Elaeis guineensis Jacq.) seedlings subjected to water stress and recovery were investigated in a greenhouse experiment. At 24 days after imposition of stress, leaf water potential in water-stressed seedlings was doubled compared to that of control and there was a drastic decline in gas-exchange parameters viz. photosynthesis, transpiration, and stomatal conductance. Water stress did not irreversibly affect gas-exchange parameters and quantum efficiency of photosystem II, as seedlings exhibited total recovery of photosynthetic apparatus by 12^th day of rehydration. These findings indicate that oil palm exhibits physiological plasticity to water stress during the seedling stage.     

Stomatal action directly feeds back on leaf turgor: new insights into the regulation of the plant water status from non‐invasive pressure probe measurements

Uptake of CO₂ by the leaf is associated with loss of water. Control of stomatal aperture by volume changes of guard cell pairs optimizes the efficiency of water use. Under water stress, the protein kinase OPEN STOMATA 1 (OST1) activates the guard‐cell anion release channel SLOW ANION CHANNEL‐ASSOCIATED 1 (SLAC1), and thereby triggers stomatal closure. Plants with mutated OST1 and SLAC1 are defective in guard‐cell turgor regulation. To study the effect of stomatal movement on leaf turgor using intact leaves of Arabidopsis, we used a new pressure probe to monitor transpiration and turgor pressure simultaneously and non‐invasively. This probe permits routine easy access to parameters related to water status and stomatal conductance under physiological conditions using the model plant Arabidopsis thaliana. Long‐term leaf turgor pressure recordings over several weeks showed a drop in turgor during the day and recovery at night. Thus pressure changes directly correlated with the degree of plant transpiration. Leaf turgor of wild‐type plants responded to CO₂, light, humidity, ozone and abscisic acid (ABA) in a guard cell‐specific manner. Pressure probe measurements of mutants lacking OST1 and SLAC1 function indicated impairment in stomatal responses to light and humidity. In contrast to wild‐type plants, leaves from well‐watered ost1 plants exposed to a dry atmosphere wilted after light‐induced stomatal opening. Experiments with open stomata mutants indicated that the hydraulic conductance of leaf stomata is higher than that of the root–shoot continuum. Thus leaf turgor appears to rely to a large extent on the anion channel activity of autonomously regulated stomatal guard cells.     

Stomatal sensitivities to changes in leaf water potential, air humidity, CO2 concentration and light intensity, and the effect of abscisic acid on the sensitivities in six temperate deciduous tree species

To characterise the stomata of six temperate deciduous tree species, sets of stomatal sensitivities to all the most important environmental factors were measured. To compare the importance of abscisic acid (ABA) in the different stomatal responses, the effect of exogenous ABA on all the stomatal sensitivities was determined.Almost all the stomatal sensitivities: the sensitivity to a decrease in leaf water potential, air humidity, CO₂ concentration ([CO₂]) and light intensity, and to an increase in [CO₂] and light intensity were the highest in the slow-growing species, and the lowest in the fast-growing species. Drought increased the sensitivity to the environmental changes that induce a decrease in the stomatal conductance, and decreased the sensitivity to the changes that induce an increase in this conductance. The sensitivities of the slow-growers were most strongly affected by drought and ABA. Therefore the success of the slow-growers in their ecological niches can be based on the highly sensitive and strictly regulated responses of their stomata. The fast-growers had the highest sensitivity to an increase in leaf water potential and this sensitivity was sharply reduced by drought and ABA. Thus, the dominance of the trees in riparian areas can be based on the ability of their stomata to quickly reach high conductance in well-watered conditions and to efficiently decrease this rate during drought.Stomatal sensitivities to the hydraulic environmental factors (water potentials in plant and air) had higher values in well-watered trees and a more pronounced response to drought than the sensitivities to the photosynthetic environmental factors ([CO₂] and light intensity). Thus, the hydraulic factors most likely prevail over the photosynthetic factors in determining stomatal conductance in these species.In response to exogenous ABA, the rates of stomatal closure, following a decrease in air humidity and light intensity, and an increase in [CO₂], were accelerated. Stomatal opening following an increase in air humidity and light intensity and a decrease in [CO₂] was replaced by slow closing. The rate of stomatal opening following an increase in leaf water potential was reduced. As the sensitivities to changes in light were modified less by the ABA than the other stomatal sensitivities, the prediction of stomatal responses on the basis of the sensitivity to light alone should be excluded in stomatal models.