The photosynthetic characteristics of papyrus in a tropical swamp

Summary Photosynthesis and transpiration was measured in the large emergent C₄ sedge Cyperus papyrus (papyrus) which occupies wide areas of wetland on the African continent. The maximum observed value of net assimilation was 35 mol CO₂ m^-2 s^-1 at full sunlight but light saturation of photosynthesis did not occur. The quantum yield of photosynthesis obtained from the initial slope of the light response curves (0.06 mol mol^-1 incident light) was relatively high and close to previously recorded values for some C₄ grasses. Measurements made over two days showed that stomatal conductance was sensitive to the ambient air vapour pressure deficit (VPD) and was consistently lower on the day when VPD's were higher. There was, however, no marked midday closure of the stomata. Photosynthesis was also reduced on the day when VPD's were higher. The relationship between net photosynthesis and stomatal conductance was close to linear over the range of measurement conditions, with the result that intercellular CO₂ concentrations (C _i ) did not vary markedly. There was some evidence that C _i decreased at high VPD's. The regulation of stomatal movement in papyrus appears to minimise excessive water loss while not severely limiting photosynthesis. The significance of this strategy for a wetland species with plentiful supplies of water is discussed.     

Nonstomatal inhibition of photosynthesis by water stress. Reduction in photosynthesis at high transpiration rate without stomatal closure in field-grown tomato

Large underestimates of the limitation to photosynthesis imposed by stomata can occur because of an error in the standard method of calculating average substomatal pressures of carbon dioxide when heterogeneity of those pressures occurs across a leaf surface. Most gas exchange data supposedly indicating nonstomatal inhibition of photosynthesis by water stress could have this error. However, if no stomatal closure occurs, any reduction in photosynthesis must be due to nonstomatal inhibition of photosynthesis. Net carbon dioxide exchange rates and conductances to water vapor were measured under field conditions in upper canopy leaves of tomato plants during two summers in Beltsville, Maryland, USA. Comparisons were made near midday at high irradiance between leaflets in air with the ambient water vapor content and in air with a higher water content. The higher water content, which lowered the leaf to air water vapor pressure difference (VPD), was imposed either one half hour or several hours before measurements of gas exchange. In both seasons, and irrespective of the timing of the imposition of different VPDs, net photosynthesis increased 60% after decreasing the VPD from 3 to 1 kPa. There were no differences in leaf conductance between leaves at different VPDs, thus transpiration rates were threefold higher at 3 than at 1 kPa VPD. It is concluded that nonstomatal inhibition of photosynthesis did occur in these leaves at high transpiration rate.     

Effect of drought and rewatering on photosynthetic physioecological characteristics of soybean

Field experiments were conducted on soybean Glycine max, yudou29, a major cultivated variety in the Henan Province of China to study the relationship between photosynthetic characteristics and other physioecological parameters of its leaves under soil drying and rewatering treatments. The study showed that the dawn water potential of soybean leaves under the drying treatment was very close to that of soybean leaves under well-watered treatments (CK) when soil water content was higher than 47% of field water capacity (FWC). But when soil water content dropped below 47% of FWC, the leaf water potential decreased rapidly, indicating a significant threshold reaction. The dawn water potential threshold of soybean leaves was about ?1.02 MPa. Below this, the leaf water potential and net photosynthesis ratio dropped rapidly. When the soil water content was 47%, the leaf water potential and net photosynthesis ratio were nearly as high as those in CK, but the transpiration ratio was 67% lower, indicating that transpiration was more sensitive to drought than photosynthesis. After rewatering, the water status of soybean leaves improved, the net photosynthesis ratio and transpiration ratio increased linearly, and leaf stomata conductance (Gs) also recovered quickly. These results showed that after stress removal, soybean had fast-growing characteristics.     

Stomatal responses to long-term high vapor pressure deficits mediated most limitation of photosynthesis in tomatoes

Plants grown at high vapor pressure deficit (VPD) usually present decreased photosynthesis, but stomatal and mesophyll limitation to photosynthesis remain poorly quantified. To better understand the regulation of high VPD on photosynthesis and plant growth in tomatoes, we investigated the limitation of stomatal conductance and mesophyll conductance to photosynthesis and relative importance of stomatal morphology and function in stomatal conductance. Both the net photosynthesis rate and total biomass were significantly limited by high VPD. Meanwhile, stomatal conductance and mesophyll conductance were decreased under high VPD. The stomatal conductance limitation was responsible for 60% of the total photosynthetic limitation. Moreover, a reduction in stomatal density and stomatal size occurred under high VPD, which was significantly correlated with the down-regulation of stomatal conductance. The stomatal morphology contributed to more than half the change in stomatal conductance. Nevertheless, stomatal movement was also an important factor in regulating stomatal conductance. The decrease of hydraulic conductance and transpiration rate with no significant difference in relative water content, leaf water potential, and/or osmotic potential suggested passive hydraulic regulation in the feedforward responses of stomata to high VPD.     

Transpiration efficiency of the grapevine cv. Semillon is tied to VPD in warm climates

Water‐use efficiency in grapevines is dependent on the aerial and below‐ground environment of the plant. Specifically, transpiration efficiency, the ratio of net carbon fixation to water loss, may be influenced by soil moisture and the leaf‐to‐air vapour pressure deficit (VPD) in the soil–plant–atmosphere continuum. The interactive effect of these abiotic parameters, however, has not been suitably investigated in field‐grown grapevines. Accordingly, gas exchange of an anisohydric variety, Semillon, was assessed across a number of vineyards in two warm grape‐growing regions of New South Wales (NSW) to ascertain how soil moisture and VPD interact to affect transpiration efficiency at the leaf level. Leaf gas exchange measurements demonstrated that the rate of transpiration (E) was driven by VPD, particularly under high soil moisture. Both high VPD and low soil moisture decreased photosynthesis (A) and instantaneous leaf transpiration efficiency (A/E). Increased intrinsic leaf transpiration efficiency (A/g) in response to drying soil was limited to vines growing in a non‐irrigated vineyard. In this site, A/g was negatively related to vine water status. VPD did not have a substantial influence on A/g in any vineyard. While VPD is the main driver for A/E, soil moisture is an important determinant of A/g. Under high VPD, stomatal closure in Semillon leaves was not substantial enough to suitably curtail transpiration, and as a consequence A/E declined. These data indicate that in warm climates, irrigation scheduling of anisohydric varieties must take into account both VPD and soil moisture so that vine water status can be maintained.     

The effect of blue light on stomatal oscillations and leaf turgor pressure in banana leaves

Stomatal oscillations are cyclic opening and closing of stomata, presumed to initiate from hydraulic mismatch between leaf water supply and transpiration rate. To test this assumption, mismatches between water supply and transpiration were induced using manipulations of vapour pressure deficit (VPD) and light spectrum in banana (Musa acuminata). Simultaneous measurements of gas exchange with changes in leaf turgor pressure were used to describe the hydraulic mismatches. An increase of VPD above a certain threshold caused stomatal oscillations with variable amplitudes. Oscillations in leaf turgor pressure were synchronized with stomatal oscillations and balanced only when transpiration equaled water supply. Surprisingly, changing the light spectrum from red and blue to red alone at constant VPD also induced stomatal oscillations – while the addition of blue (10%) to red light only ended oscillations. Blue light is known to induce stomatal opening and thus should increase the hydraulic mismatch, reduce the VPD threshold for oscillations and increase the oscillation amplitude. Unexpectedly, blue light reduced oscillation amplitude, increased VPD threshold and reduced turgor pressure loss. These results suggest that additionally, to the known effect of blue light on the hydroactive opening response of stomata, it can also effect stomatal movement by increased xylem–epidermis water supply.     

Changes in the Water Balance and Photosynthesis of Onion, Bean and Cotton Plants under Saline Conditions

The osmotic concentration (osmotic potential) of onion leaf sap did not adjust to chloride salinity, and consequently water potential, turgor, stomatal aperture and transpiration were reduced. Although osmotic concentration of bean and cotton leaf sap did adjust to a saline root medium and turgor was no less in the salinized plants than in the controls, stomata of the salinized plants remained only partly open and transpiration was reduced. Net photosynthesis of onion plants was reduced by salinity (this effect being much enhanced in a hot dry atmosphere) but it could be rapidly raised to the level of the controls by inducing elevated leaf turgor. Stomatal closure was initially responsible for most of the ～30 % reduction in photosynthesis of salinized beans. This was due to interference with CO₂ diffusion and could be overcome by raising the CO₂ concentration in the air. At a later stage of growth, salinity affected the light reaction of bean photosynthesis, and elevation of the air CO₂ had little effect. Closure of stomata of salinized cotton plants had only a relatively small effect on net photosynthesis. Light intensity and CO₂ concentration experiments showed that salinity was reducing the photosynthesis of cotton leaves mainly by affecting the light reaction of photosynthesis. It is concluded that chloride salinity does affect the water balance and rate of photosynthesis of plants and that the nature and degree of the effects will depend upon climatic conditions and may be very different between plant species and in the same species at different periods of growth.     

Stomatal response to air humidity and its relation to stomatal density in a wide range of warm climate species

The gas exchange of 19 widely different warm climate species was observed at different leaf to air vapour pressure deficits (VPD). In all species stomata tended to close as VPD increased resulting in a decrease in net photosynthesis. The absolute reduction in leaf conductance per unit increase in VPD was greatest in those species which had a large leaf conductance at low VPDs. This would be expected even if stomata of all species were equally sensitive. However the percentage reduction in net photosynthesis (used as a measure of the relative sensitivity of stomata of the different species) was also closely related to the maximal conductance at low VPD. Similarily the relative sensitivity of stomata to changes in VPD was closely related to the weighted stomatal density or crowding index.The hypothesis is presented that stomatal closure at different VPDs is related to peristomatal evaporation coupled with a high resistance between the epidermis and the mesophyll and low resistance between the stomatal apparatus and the epidermal cells. This hypothesis is consistent with the greater relative sensitivity of stomata on leaves with a high crowding index.The results and the hypothesis are discussed in the light of selection, for optimal productivity under differing conditions of relative humidity and soil water availablility, by observation of stomatal density and distribution on the two sides of the leaf.Visiting scientist, plant physiologist and research assitant of the Cassava Program     

High vapour pressure deficit exacerbates xylem cavitation and photoinhibition in shade-grown Piper auritum H.B. & K. during prolonged sunflecks

Water relations dynamics during simulated sunflecks at high (36°C) and medium (27°C) temperatures and high and low vapour pressure deficits beween leaf and air (VPD) were studied on shade-grown Piper auritum H.B. & K. plants, a pioneer tree, common in gaps and clearings of tropical rain forests. The leaves of P. auritum wilt rapidly when exposed to high light. Exposure to high VPD and high light caused substantial and rapid dehydration of leaves. Dehydration could be prevented under high humidity irrespective of temperature. Water stored in leaf cells served as initial source for transpiration upon high light exposure. This effect increased with increasing VPD and temperature. The pronounced decrease in leaf water content over time in high light caused a rapid decrease in leaf water potential (Ψ_l) and a concomitant increase in water potential gradient (ΔΨ/Δx) between trunk and leaf, yet the high leaf elasticity (small bulk elastic modulus, ε) allowed turgor maintenance under most conditions. Under high VPD and high temperature, stomata remained open and ΔΨ/Δx frequently exceeded 0.95 MPa · m⁻¹, the cavitation-inducing threshold (ΔΨ/Δx _cav) causing high rates of acoustic emissions from stems and leaf petioles and leading to concomitant losses in hydraulic conductance per leaf area (k _l). At medium temperature (high VPD), stomatal closure contained xylem embolism by keeping ΔΨ/Δx at or below this threshold. We argue that wilting substantially contributes to creating a sufficient driving force for water uptake from the soil, and reducing the VPD (through a decrease in radiation load and thus leaf temperature) to avoid excessive dehydration. Received: 3 March 1996 / Accepted: 10 November 1996     

The responses of stomata and leaf gas exchange to vapour pressure deficits and soil water content

The responses of leaf conductance, leaf water potential and rates of transpiration and net photosynthesis at different vapour pressure deficits ranging from 10 to 30 Pa kPa^-1 were followed in the sclerophyllous woody shrub Nerium oleander L. as the extractable soil water content decreased. When the vapour pressure deficit around a plant was kept constant at 25 Pa kPa^-1 as the soil water content decreased, the leaf conductance and transpiration rate showed a marked closing response to leaf water potential at-1.1 to-1.2 MPa, whereas when the vapour pressure deficit around the plant was kept constant at 10 Pa kPa^-1, leaf conductance decreased almost linearly from-0.4 to-1.1 MPa. Increasing the vapour pressure deficit from 10 to 30 Pa kPa^-1 in 5 Pa kPa^-1 steps, decreased leaf conductance at all exchangeable soil water contents. Changing the leaf water potential in a single leaf by exposing the remainder of the plant to a high rate of transpiration decreased the water potential of that leaf, but did not influence leaf conductance when the soil water content was high. As the soil water content was decreased, leaf conductances and photosynthetic rates were higher at equal levels of water potential when the decrease in potential was caused by short-term increases in transpiration than when the potential was decreased by soil drying.As the soil dried and the stomata closed, the rate of photosynthesis decreased with a decrease in the internal carbon dioxide partial pressure, but neither the net photosynthetic rate nor the internal CO₂ partial pressure were affected by low water potentials resulting from short-term increases in the rate of transpiration. Leaf conductance, transpiration rate and net photosynthetic rate showed no unique relationship to leaf water potential, but in all experiments the leaf gas exchange decreased when about one half of the extractable soil water had been utilized. We conclude that soil water status rather than leaf water status controls leaf gas exchange in N. oleander.     

Sheathing the blade: Significant contribution of sheaths to daytime and nighttime gas exchange in a grass crop

Despite representing a sizeable fraction of the canopy, very little is known about leaf sheath gas exchange in grasses. Specifically, estimates of sheath stomatal conductance, transpiration and photosynthesis along with their responses to light, CO₂ and vapour pressure deficit (VPD) are unknown. Furthermore, the anatomical basis of these responses is poorly documented. Here, using barley as a model system, and combining leaf-level gas exchange, whole-plant gravimetric measurements, transpiration inhibitors, anatomical observations, and biophysical modelling, we found that sheath and blade stomatal conductance and transpiration were similar, especially at low light, in addition to being genotypically variable. Thanks to high abaxial stomata densities and surface areas nearly half those of the blades, sheaths accounted for up to 17% of the daily whole-plant water use, which -surprisingly- increased to 45% during the nighttime. Sheath photosynthesis was on average 17–25% that of the blade and was associated with lower water use efficiency. Finally, sheaths responded differently to the environment, exhibiting a lack of response to CO₂ but a strong sensitivity to VPD. Overall, these results suggest a key involvement of sheaths in feedback loops between canopy architecture and gas exchange with potentially significant implications on adaptation to current and future climates in grasses.     

The Effect of Leaf Water Potential, Leaf Temperature and Light Intensity on Leaf Diffusion Resistance and the Transpiration of Leaves of Malus sylvestris

The relationship between leaf resistance to water vapour diffusion and each of the factors leaf water potential, light intensity and leaf temperature was determined for leaves on seedling apple trees (Malus sylvestris Mill. cv. Granny Smith) in the laboratory. Leaf cuticular resistance was also determined and transpiration was measured on attached leaves for a range of conditions. Leaf resistance was shown to be independent of water potential until potential fell below — 19 bars after which leaf resistance increased rapidly. Exposure of leaves to CO₂-free air extended the range for which resistance was independent of water potential to — 30 bars. The light requirement for minimum leaf resistance was 10 to 20 W m^?2 and at light intensities exceeding these, leaf resistance was unaffected by light intensity. Optimum leaf temperature for minimum diffusion resistance was 23 ± 2°C. The rate of change measured in leaf resistance in leaves given a sudden change in leaf temperature increased as the magnitude of the temperature change increased. For a sudden change of 1°C in leaf temperature, diffusion resistance changed at a rate of 0.01 s cm^?1 min^?1 whilst for a 9°C leaf temperature change, diffusion resistance changed at a rate of 0.1 s cm^?1 min^?1. Cuticular resistance of these leaves was 125 s cm^?1 which is very high compared with resistances for open stomata of 1.5 to 4 s cm^?1 and 30 to 35 s cm^?1 for stomata closed in the dark. Transpiration was measured in attached apple leaves enclosed in a leaf chamber and exposed to a range of conditions of leaf temperature and ambient water vapour density. Peak transpiration of approximately 5 × 10^?6 g cm^?2 s^?1 occurred at a vapour density gradient from the leaf to the air of 12 to 14 g m^?3 after which transpiration declined due presumably to increased stomatal resistance. Leaves in CO₂-free air attained a peak transpiration of 11 × 10^?6 g cm^?2 s^?1 due to lower values of leaf resistance in CO₂ free air. Transpiration then declined in these leaves due to development of an internal leaf resistance (of up to 2 s cm^?1). The internal resistance was masked in leaves at normal CO₂ concentrations by the increase in stomatal resistance.     

Increased leaf area dominates carbon flux response to elevated CO2 in stands of Populus deltoides (Bartr.)

We examined the effects of atmospheric vapor pressure deficit (VPD) and soil moisture stress (SMS) on leaf‐ and stand‐level CO₂ exchange in model 3‐year‐old coppiced cottonwood (Populus deltoides Bartr.) plantations using the large‐scale, controlled environments of the Biosphere 2 Laboratory. A short‐term experiment was imposed on top of continuing, long‐term CO₂ treatments (43 and 120 Pa), at the end of the growing season. For the experiment, the plantations were exposed for 6–14 days to low and high VPD (0.6 and 2.5 kPa) at low and high volumetric soil moisture contents (25–39%). When system gross CO₂ assimilation was corrected for leaf area, system net CO₂ exchange (SNCE), integrated daily SNCE, and system respiration increased in response to elevated CO₂. The increases were mainly as a result of the larger leaf area developed during growth at high CO₂, before the short‐term experiment; the observed decline in responses to SMS and high VPD treatments was partly because of leaf area reduction. Elevated CO₂ ameliorated the gas exchange consequences of water stress at the stand level, in all treatments. The initial slope of light response curves of stand photosynthesis (efficiency of light use by the stand) increased in response to elevated CO₂ under all treatments. Leaf‐level net CO₂ assimilation rate and apparent quantum efficiency were consistently higher, and stomatal conductance and transpiration were significantly lower, under high CO₂ in all soil moisture and VPD combinations (except for conductance and transpiration in high soil moisture, low VPD). Comparisons of leaf‐ and stand‐level gross CO₂ exchange indicated that the limitation of assimilation because of canopy light environment (in well‐irrigated stands; ratio of leaf : stand=3.2–3.5) switched to a predominantly individual leaf limitation (because of stomatal closure) in response to water stress (leaf : stand=0.8–1.3). These observations enabled a good prediction of whole stand assimilation from leaf‐level data under water‐stressed conditions; the predictive ability was less under well‐watered conditions. The data also demonstrated the need for a better understanding of the relationship between leaf water potential, leaf abscission, and stand LAI.     

Diurnal Expansion and Contraction of Leaves and Fruits of English Morello Cherry

Changes in leaf thickness and fruit diameter were measured ingrowth chambers under varying conditions of light, humidity,temperature, and soil moisture for potted trees of English Morellocherry (Prunus cerasus L. grafted on Prunus mahaleb root stock).Decrease in leaf thickness of well-watered plants was inducedby illumination following a period of darkness. In the light,leaf thickness decreased when vapour-pressure deficit (VPD)was rising or high. The magnitude of diurnal change in leafthickness was related to amount of change in VPD of the air.Leaf thickness increased in the dark when stomata were closed.When changes in VPD were minimized, leaves under 8-h days and16-h nights still decreased in thickness during the day andexpanded at night, but the degree of change was not as greatas when VPD also fluctuated diurnally. When severe internal water deficits developed in trees duringprolonged droughts the correlations of changes in leaf thicknesswith VPD and light intensity were low. Marked decline in leafthickness resulted with little re-expansion in the dark at lowVPD. Soil irrigation resulted in rapid hydration and expansionof leaves. Changes in fruit diameter in contrast were positivelycorrelated with VPD fluctuations and were not influenced byphotoperiod.     

Diurnal and Seasonal Changes in Water Balance of Acer saccharum and Betula papyrifera

Diurnal and seasonal changes in plant water potential, leaf diffusion resistance, and stem radial changes of Acer saccharum and Betula papyrifera trees were studied in northern Wisconsin during the 1974 and 1975 growing seasons. Water potential decreased during the day, following relatively high values in the morning, and increased in the late afternoon and evening. Diurnal patterns and actual values of water potential varied with species, soil water availability, and factors influencing transpiration (e.g., solar radiation, vapor pressure deficit, and transpiration flux density). When plant water deficits were not severe, leaf resistance of both species was rather stable during the day. During severe droughts, however, leaf resistance increased (stomata closed) during the day when light intensity was high. Leaf resistance at high light intensity was higher in Acer than in Betula. Stomatal closure with decreasing light intensity varied between species and among Acer trees. Tree stems of both species shrank during the day, as internal water deficits developed, and they expanded as trees rehydrated during the night. Stems of Acer shrank more than those of Betula. The amount of daily stem shrinkage increased as the season progressed if the trees were not under severe water deficits. During severe droughts the amount of diurnal stem shrinkage decreased. Shrinkage of stems lagged behind water potential changes by 1 to 2 h in Acer and less than 1 h in Betula. The relationship between stem radius and leaf water potential was not constant throughout the growing season.     

Mechanisms of stomatal movement in response to air humidity,irradiance and xylem water potential

Turgor, and osmotic and water potentials of subsidiary cells, epidermal cells and mesophyll cells were measured with a pressure probe and a nanoliter osmometer in intact transpiring leaves of Tradescantia virginiana L. Xylem water potential was manipulated by changing air humidity, light, and water supply. In a transpiring leaf the water potential of mesophyll cells was lower, but turgor was higher, than in cells surrounding the stomatal cavity owing to the presence of a cuticle layer which covers the internal surface of subsidiary and guard cells. Cuticular transpiration from the outer leaf surface was negligibly small. When stomata closed in dry air, transpiration decreased despite an increasing vapor-pressure difference between leaf and air, and the water potential of subsidiary cells dropped to the level of the water potential in mesophyll cells. We suggest that the observed decrease of transpiration at increasing vapor-pressure difference can be attributed to a shortage of water supply to the guard cells from subsidiary cells, causing turgor to decrease in the former more than in the latter. The leafs internal cuticle appears to play a special role in channelling the internal water flow during a water shortage.Abbreviations and Symbols VPD Vapor-pressure difference between leaf and air - PFD photon flux density - water potential     

Acclimation to humidity modifies the link between leaf size and the density of veins and stomata

The coordination of veins and stomata during leaf acclimation to sun and shade can be facilitated by differential epidermal cell expansion so large leaves with low vein and stomatal densities grow in shade, effectively balancing liquid‐ and vapour‐phase conductances. As the difference in vapour pressure between leaf and atmosphere (VPD) determines transpiration at any given stomatal density, we predict that plants grown under high VPD will modify the balance between veins and stomata to accommodate greater maximum transpiration. Thus, we examined the developmental responses of these traits to contrasting VPD in a woody angiosperm (Toona ciliata M. Roem.) and tested whether the relationship between them was altered. High VPD leaves were one‐third the size of low VPD leaves with only marginally greater vein and stomatal density. Transpirational homeostasis was thus maintained by reducing stomatal conductance. VPD acclimation changed leaf size by modifying cell number. Hence, plasticity in vein and stomatal density appears to be generated by plasticity in cell size rather than cell number. Thus, VPD affects cell number and leaf size without changing the relationship between liquid‐ and vapour‐phase conductances. This results in inefficient acclimation to VPD as stomata remain partially closed under high VPD.     

The Effect of Drought and Vapour Pressure Deficit on Gas Exchange of Young Kiwifruit (Actinidia deliciosavar.deliciosa) Vines

To evaluate the effect of drought and vapour pressure deficit (VPD) on stomatal behaviour and gas exchange parameters, young kiwifruit vines (Actinidia deliciosavar.deliciosacv. Hayward) were exposed to alternating periods of drought and drought-relief over two growing seasons. Vines were grown either in the field or in containers. Stomatal conductance of fully-expanded leaves rapidly decreased as pre-dawn leaf water potential was reduced below a threshold value of -0.3MPa. Stomatal conductance reached minimum values of 10–20mmol m^-2s^-1. Transpiration rate was similarly sensitive to changes in leaf water status, whereas more severe drought levels were necessary to affect photosynthesis significantly. Net daily carbon gains were estimated at 4.7 and 2.7gm^-2for irrigated and droughted vines, respectively. Gas exchange parameters recovered to values of irrigated vines within a few hours after relief of stress. Rate of recovery depended on the level of stress reached during the previous drought period. There was a steady decline in stomatal conductance when VPD was increased from 0.8 to 2.5kPa in both irrigated and droughted vines. The VPD at which stomatal conductance reached 50% of maximum values was 2.1–2.2kPa for both treatments. We conclude that stomata were highly sensitive to changes in soil water status and that midday depression of photosynthesis measured in kiwifruit vines was related to water deficits arising in the leaf because of both transpirational losses and to the direct effect of increasing VPD.     

Rapid and Specific Modulation of Stomatal Conductance by Blue Light in Ivy (Hedera helix) : An Approach to Assess the Stomatal Limitation of Carbon Assimilation

Low intensity (0.015 millimole per square meter per second) blue light applied to leaves of Hedera helix under a high intensity red light background (0.50 millimole per square meter per second red light) induced a specific stomatal opening response, with rapid kinetics comparable to those previously reported for stomata with `grass type' morphology. The response of stomatal conductance to blue light showed a transient `overshoot' behavior at high vapor pressure difference (2.25 ± 0.15 kiloPascals), but not at low vapor pressure difference (VPD) (0.90 ± 0.10 kilo-Pascal). The blue light-induced conductance increase was accompanied by an increase in net photosynthetic carbon assimilation, mediated by an increase in the intercellular concentration of carbon dioxide. Values of assimilation once the blue light-stimulated conductance increase reached steady state were less than those at the peak of the overshoot, but the ratios of assimilation to transpiration (A/E) and blue light-stimulated ΔA/ΔE were greater during the steady-state response than during the overshoot. These results indicate that significant stomatal limitation of assimilation can occur, but that this limitation may improve water use efficiency under high VPD conditions. Under high intensity red light, the decline in A/E associated with an increase in VPD was minimized when conductance was stimulated by additional low intensity blue light. This effect indicates that the blue light response of stomata may be important in H. helix for the optimization of water use efficiency under natural conditions of high irradiance and VPD.     

The magnitude of the stomatal response to blue light : modulation by atmospheric humidity

The effect of leaf-air vapor pressure difference (VPD) on the magnitude of the stomatal response to blue light was investigated in soybean (Glycine max) by administering blue light pulses (22 seconds by 120 micromoles per square meter per second) at different levels of VPD and temperature. At 20 °C and 25 °C, the magnitude of the integrated conductance response decreased with increasing VPD (0.4 to 2.6 kiloPascals), due to an earlier onset of stomatal closure that terminated the pulse response. In contrast, at 30 °C this magnitude increased with rising VPD (0.9 to 3.5 kiloPascals), due to an increasing maximum excursion of the conductance response despite the accelerated onset of stomatal closure. When the feedforward response of stomata to humidity caused steady state transpiration to decrease with increasing VPD, the magnitude of the pulse-induced conductance response correlated with VPD rather than with transpiration. This suggests that water relations or metabolite movements within epidermal rather than bulk leaf tissue interacted with guard cell photobiological properties in regulating the magnitude of the blue light response. VPD modulation of pulse magnitude could reduce water loss during stomatal responses to transient illumination in natural light environments.