THE MECHANISM OF STOMATAL MOVEMENT

Ketellapper , H. J. (California Inst. Tech., Pasadena.) The mechanism of stomatal movement. Amer. Jour. Bot. 46(3) : 225-231. IIlus. 1959.—A review of the pertinent literature reveals that fairly exact knowledge is available about the effects of light, CO₂, and water content of the leaf on stomatal movement. Two distinct types of light action can be distinguished: an indirect effect, mediated through photosynthesis and the resulting lower CO₂ concentration within the leaf, and a direct effect which occurs even when the intercellular spaces are washed out with CO₂-free air. The CO₂ concentration occupies a very central position in the regulation of stomatal movement. The action of CO₂ and light will be influenced, or even counteracted, by the value of the water deficit in the leaf. A large number of changes in the guard cells, accompanying stomatal movement, has been described in the literature and some of these have been discussed in the present review: for example, the changes in osmotic value, in starch content, and in permeability. These observations led to the formulation of the classical theories of stomatal movement. It has been concluded that the classical theories are not adequate to explain stomatal movement. At present one can choose between 2 alternatives: an osmotic theory incorporating the pathways of the classical theories and bringing these together in one general scheme hinging on the sugar-starch conversion, or else a theory incorporating non-osmotic processes for the removal of water or osmotic active material. These alternatives have been discussed in some detail. It has been concluded that more experimental evidence is required before a valid theory of stomatal movement can be brought forward.     

Do Stomata Respond to CO(2) Concentrations Other than Intercellular?

Most studies on stomatal responses to CO₂ assume that guard cells respond only to intercellular CO₂ concentration and are insensitive to the CO₂ concentrations in the pore and outside the leaf. If stomata are sensitive to the CO₂ concentration at the surface of the leaf or in the stomatal pore, the stomatal response to intercellular CO₂ concentration will be incorrect for a `normally' operating leaf (where ambient CO₂ concentration is a constant). In this study asymmetric CO₂ concentrations for the two surfaces of amphistomatous leaves were used to vary intercellular and leaf surface CO₂ concentrations independently in Xanthium strumarium L. and Helianthus annuus L. The response of stomata to intercellular CO₂ concentration when the concentration at the leaf surface was held constant was found to be the same as the response when the surface concentration was varied. In addition, stomata did not respond to changes in leaf surface CO₂ concentration when the intercellular concentration for that surface was held constant. It is concluded that stomata respond to intercellular CO₂ concentration and are insensitive to the CO₂ concentration at the surface of the leaf and in the stomatal pore.     

Contrasting responses of leaf stomatal characteristics to climate change: a considerable challenge to predict carbon and water cycles

Stomata control the cycling of water and carbon between plants and the atmosphere; however, no consistent conclusions have been drawn regarding the response of stomatal frequency to climate change. Here, we conducted a meta‐analysis of 1854 globally obtained data series to determine the response of stomatal frequency to climate change, which including four plant life forms (over 900 species), at altitudes ranging from 0 to 4500 m and over a time span of more than one hundred thousand years. Stomatal frequency decreased with increasing CO₂ concentration and increased with elevated temperature and drought stress; it was also dependent on the species and experimental conditions. The response of stomatal frequency to climate change showed a trade‐off between stomatal control strategies and environmental factors, such as the CO₂ concentration, temperature, and soil water availability. Moreover, threshold effects of elevated CO₂ and temperature on stomatal frequency were detected, indicating that the response of stomatal density to increasing CO₂ concentration will decrease over the next few years. The results also suggested that the stomatal index may be more reliable than stomatal density for determination of the historic CO₂ concentration. Our findings indicate that the contrasting responses of stomata to climate change bring a considerable challenge in predicting future water and carbon cycles.     

Integration of hydraulic and chemical signalling in the control of stomatal conductance and water status of droughted plants

We describe here an integration of hydraulic and chemical signals which control stomatal conductance of plants in drying soil, and suggest that such a system is more likely than control based on chemical signals or water relations alone. The determination of xylem [ABA] and the stomatal response to xylem [ABA] are likely to involve the water flux through the plant. (1) If, as seems likely, the production of a chemical message depends on the root water status (Ψ_r), it will not depend solely on the soil water potential (Ψ_s) but also on the flux of water through the soil-plant-atmosphere continuum, to which are linked the difference between Ψ_r and Ψ_s. (2) The water flux will also dilute the concentration of the message in the xylem sap. (3) The stomatal sensitivity to the message is increased as leaf water potential falls. Stomatal conductance, which controls the water flux, therefore would be controlled by a water-flux-dependent message, with a water-flux-dependent sensitivity. In such a system, we have to consider a common regulation for stomatal conductance, leaf and root water potentials, water flux and concentration of ABA in the xylem. In order to test this possibility, we have combined equations which describe the generation and effects of chemical signals and classical equations of water flux. When the simulation was run for a variety of conditions, the solution suggested that such common regulation can operate. Simulations suggest that, as well as providing control of stomatal conductance, integration of chemical and hydraulic signalling may also provide a control of leaf water potential and of xylem [ABA], features which are apparent from our experimental data. We conclude that the root message would provide the plant with a means to sense the conditions of water extraction (soil water status and resisance to water flux) on a daily timescale, while the short-term plant response to this message would depend on the evaporative demand.     

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.     

Hormonal Interactions and Stomatal Responses

Both environmental and hormonal factors and their interactions affect stomatal behavior. Methodologies for identifying hormonal interactions affecting stomatal function are reviewed. Although there is abundant evidence that abscisic acid (ABA) closes stomata, evidence that the other classical plant hormones (auxins, cytokinins, ethylene, gibberellins) in isolation alter stomatal response often comes from exogenous applications to detached epidermes and leaves, rather than correlation of endogenous concentrations with stomatal conductance (g_s). Evidence for hormonal interactions comes from isolated tissues with exogenous hormones supplied at nonphysiological concentrations, or from variation in stomatal response to xylem ABA concentration in planta. The roles of hormonal changes in causing stomatal closure following changes in soil environment are considered. Although soil drying induces multiple changes in xylem sap composition, analysis of stomatal responses suggests a dominant role for increased endogenous ABA concentrations and relatively little evidence of roles for other hormones. A similar picture emerges from studies of soil compaction. Although soil flooding decreases ABA export from the root system, there is some evidence that apoplastic ABA accumulation elicits stomatal closure. Stomatal closure following nitrogen deprivation does not appear to involve ABA and may provide a suitable experimental system to investigate roles for other hormones. The availability of mutant or transgenic lines with altered hormone homeostasis or sensitivity provides opportunities to screen for altered stomatal behavior in response to different environments, and may provide new evidence that hormonal interactions are important in the control of stomatal behavior.     

A three-dimensional model of CO2 transport in airspaces and mesophyll cells of a silver birch leaf

A realistic numerical three‐dimensional (3D) model was constructed to study CO₂ transport inside a birch leaf. The model included chloroplasts, palisade and spongy mesophyll cells, airspaces, stomatal opening and the leaf boundary layer. Diffusion equations for CO₂ were solved for liquid(mesophyll) and gaseous(air) phases. Simulations were made in typical ambient field conditions varying stomatal opening, photosynthetic capacity and temperature. Doubled ambient CO₂ concentration was also considered. Changes in variables caused non‐linear effects in the total flux, especially when compared with the results of double CO₂ concentration. The reduction in stomatal opening size had a smaller effect on the total flux in doubled concentrations than ambient CO₂. The reduced photosynthetic capacity had a similar effect on the flux in both cases. The palisade and spongy mesophyll cells had unequal roles mainly due to the light absorption profile. Results from the 3D simulation were also compared to the classical one‐dimensional resistance approach. Liquid and gas phase resistances were estimated and found strongly variable according to changes in temperature and degree of stomatal opening. For the birch leaves modelled, intercellular airspace resistance was small (2% of the total resistance in saturating irradiance conditions at 25 °C at stomatal opening diameter of 4 µm) whereas the liquid phase resistance was significant (23% for mesophyll and chloroplasts in the same ‘base case’). The absorption of CO₂ into water at cell surfaces caused additional (strongly temperature dependent) resistance which accounted for 36% of the total resistance in the base case.     

植物气孔导度的机理模型

Ball-Berry气孔导度模型及其修正模型是评价植物叶片气孔调节的重要工具。该文从CO₂分子在叶片气孔中扩散这个最基本的物理过程出发, 应用物理学中的分子扩散和碰撞理论、流体力学与植物生理学等知识, 严格推导出叶片气孔导度的机理模型。利用美国Li-Cor公司生产的Li-6400光合作用测定仪控制CO₂浓度、湿度和温度, 测量了华北平原冬小麦(Triticum aestivum)的光响应数据和气孔导度数据。拟合结果表明: 推导的气孔导度机理模型较之Ball-Berry气孔导度模型和Tuzet等气孔导度模型, 能更好地描述冬小麦的气孔导度与净光合速率之间的关系。如果用气孔导度的机理模型耦合光合作用对光响应的修正模型, 则耦合模型可以很好地描述华北平原冬小麦叶片气孔导度对光强的响应曲线, 并可直接估算冬小麦的最大气孔导度和对应的饱和光强, 同时可以研究最大气孔导度是否与最大净光合速率同步的问题。拟合结果还表明: 冬小麦在30 ℃、560 μmol·mol^-1CO₂, 或在32 ℃、370 μmol·mol^-1CO₂条件下, 最大气孔导度与最大净光合速率并不同步。     

Interpretation of an empirical model for stomatal conductance in terms of guard cell function

An empirical model for stomatal conductance (g), proposed by Leuning (1995, this issue) as a modification of Ball, Woodrow & Berry's (1987) model, is interpreted in terms of a simple, steady-state model of guard cell function. In this model, stomatal aperture is a function of the relative turgor between guard cells and epidermal cells. The correlation between g and leaf surface vapour pressure deficit in Leuning's model is interpreted in terms of stomatal sensing of the transpiration rate, via changes in the gradient of total water potential between guard cells and epidermal cells. The correlation between g, CO₂ assimilation rate and leaf surface CO₂ concentration in Leuning's model is interpreted as a relationship between the corresponding osmotic gradient, irradiance, temperature, intercellular CO₂ concentration and stomatal aperture itself. The explicit relationship between osmotic gradient and stomatal aperture (possibly describing the effect of changes in guard cell volume on the membrane permeability for ion transport) results in a decrease in the transpiration rate in sufficiently dry air. Possible extension of the guard cell model to include stomatal responses to soil water status is discussed.     

Stomatal control by fed or endogenous xylem ABA in sunflower: interpretation of correlations between leaf water potential and stomatal conductance in anisohydric species

The stomatal conductance of several anisohydric plant species, including field-grown sunflower, frequently correlates with leaf water potential (φ₁), suggesting that chemical messages travelling from roots to shoots may not play an important role in stomatal control. We have performed a series of experiments in which evaporative demand, soil water status and ABA origin (endogenous or artificial) were varied in order to analyse stomatal control. Sunflower plants were subjected to a range of soil water potentials under contrasting air vapour pressure deficits (VPD, from 0.5 to 2.5 kPa) in the field, in the glasshouse or in a humid chamber. Sunflower plants were also fed through the xylem with varying concentrations of artificial ABA, in the glasshouse and in the field. Finally, detached leaves were fed directly with varying concentrations of ABA under three contrasting VPDs. A unique relationship between stomatal conductance (g_s) and the concentration of ABA in the xylem sap (xylem [ABA]) was observed in all cases. In contrast, the relationship between φ₁ and g_s varied substantially among experiments. Its slope was positive for droughted plants and negative for ABA-fed whole plants or detached leaves, and also varied appreciably with air VPD. All observed relationships could be modelled on the basis of the assumption that φ₁ had no controlling effect on g_s. We conclude that stomatal control depended only on the concentration of ABA in the xylem sap, and that φ₁ was controlled by water flux through the plant (itself controlled by stomatal conductance). The possibility is also raised that differences in stomatal ‘strategy’ between isohydric plants (such as maize, where daytime φ₁ does not vary appreciably with soil water status) and anisohydric plants (such as sunflower) may be accounted for by the degree of influence of φ₁ on stomatal control, for a given level of xylem [ABA]. We propose that statistical relationships between φ₁ and g_s are only observed when φ₁ has no controlling action on stomatal behaviour.     

Zinc mediated effects on leaf CO2 diffusion conductances and net photosynthesis in Phaseolus vulgaris L.

Supra-optimal levels of zinc in primary leaves of Phaseolus vulgaris increased the CO₂ compensation point and inhibited net photosynthesis. Leaf morphology was modified: mesophyll intercellular area, stomatal slit length and interstomatal distance were reduced, but stomatal density increased. Internal and stomatal conductances to CO₂ diffusion decreased. These changes are discussed in relation to the observed effects on leaf gas exchange and to the previously reported inhibition of different photosynthetic and photorespiratory enzymes.     

Saturation Kinetics of the Velocity of Stomatal Closing in Response to CO(2)

Stomatal closing movements in response to changes from CO₂-free to CO₂-containing air were recorded in leaf sections of Zea mays using air flow porometers. The response to CO₂ was fast; the shortest lag between the application of 300 microliters CO₂ per liter of air and the beginning of a stomatal response was 3 seconds. The velocity of stomatal closing increased with CO₂ concentration and approached its maximal value between 10³ and 10⁴ microliters CO₂ per liter of air. The CO₂ concentration at which the closing velocity reached half its maximal value was approximately 200 microliters CO₂ per liter of air, both in the light and in darkness. This indicates that the mechanism of stomatal responses to CO₂ is the same in both light regimes and that the range of stomatal sensitivity to changes in CO₂ concentration coincides with the range of CO₂ concentrations known to occur in the intercellular spaces of illuminated leaves.     

Does engineering abscisic acid biosynthesis in Nicotiana plumbaginifolia modify stomatal response to drought?

The consequences of manipulating abscisic acid (ABA) biosynthesis rates on stomatal response to drought were analysed in wild‐type, a full‐deficient mutant and four under‐producing transgenic lines of N. plumbaginifolia. The roles of ABA, xylem sap pH and leaf water potential were investigated under four experimental conditions: feeding detached leaves with varying ABA concentration; injecting exogenous ABA into well‐watered plants; and withholding irrigation on pot‐grown plants, either intact or grafted onto tobacco. Changes in ABA synthesis abilities among lines did not affect stomatal sensitivity to ABA concentration in the leaf xylem sap ([ABA]_xyl), as evidenced with exogenous ABA supplies and natural increases of [ABA]_xyl in grafted plants subjected to drought. The ABA‐deficient mutant, which is uncultivable under normal evaporative demand, was grafted onto tobacco stock and then presented the same stomatal response to [ABA]_xyl as wild‐type and other lines. This reinforces the dominant role of ABA in controlling stomatal response to drought in N. plumbaginifolia whereas roles of leaf water potential and xylem sap pH were excluded under all studied conditions. However, when plants were submitted to soil drying onto their own roots, stomatal response to [ABA]_xyl slightly differed among lines. It is suggested, consistently with all the results, that an additional root signal of soil drying modulates stomatal response to [ABA]_xyl.     

Stomatal regulation and water economy in crassulacean acid metabolism plants: an optimization model

It has been found that the stomatal behaviour of C₃ and C₄ plants can be predicted from the assumption that they increase transpiration whenever the increase δW in daily water loss is offset by a gain of at least λδW in carbon assimilation, where the minimum acceptable marginal conversion efficiency λ is determined by long term ecological factors, and is essentially constant within the course of a day. This paradigm is here extended to plants with Crassulacean acid metabolism (CAM). During daytime assimilation the results are the same as for C₃ and C₄ metabolisms. However night-time assimilation can be inhibited by the accumulation of malate in the cell vacuoles. In this event our model predicts that in a constant environment the stomatal conductance remains proportional to the square root of the mesophyll conductance as the latter declines. This is intermediate between keeping a constant stomatal conductance and keeping a constant intercellular CO₂ concentration (as tends to occur in the C₃/C₄ model when illumination varies), and results in an increasing intercellular CO₂ concentration towards the end of the night. This prediction accords with the Agave data of Nobel & Hartsock 1979. The model also predicts the allocation of time between C₃ and CAM for different degrees of water stress. The results agree qualitatively with observation, even though physiological changes (other than stomatal conductance) are not included in the model.     

Effect of Elevated Carbon Dioxide Concentration on the Stomatal Parameters of Rice Cultivars

The response of stomatal parameters of four rice cultivars to atmospheric elevated CO₂ concentration (EC) was studied using open top chambers. EC brought about reduction in stomatal conductance and increase in stomatal index, size of stomatal guard cells, stroma, and epidermal cells. Such acclimation helped the regulation of photosynthesis to EC. These changes in stomatal characters made rice cultivars adjustable to EC environment.     

Reconciling the optimal and empirical approaches to modelling stomatal conductance

Models of vegetation function are widely used to predict the effects of climate change on carbon, water and nutrient cycles of terrestrial ecosystems, and their feedbacks to climate. Stomatal conductance, the process that governs plant water use and carbon uptake, is fundamental to such models. In this paper, we reconcile two long‐standing theories of stomatal conductance. The empirical approach, which is most commonly used in vegetation models, is phenomenological, based on experimental observations of stomatal behaviour in response to environmental conditions. The optimal approach is based on the theoretical argument that stomata should act to minimize the amount of water used per unit carbon gained. We reconcile these two approaches by showing that the theory of optimal stomatal conductance can be used to derive a model of stomatal conductance that is closely analogous to the empirical models. Consequently, we obtain a unified stomatal model which has a similar form to existing empirical models, but which now provides a theoretical interpretation for model parameter values. The key model parameter, g₁, is predicted to increase with growth temperature and with the marginal water cost of carbon gain. The new model is fitted to a range of datasets ranging from tropical to boreal trees. The parameter g₁ is shown to vary with growth temperature, as predicted, and also with plant functional type. The model is shown to correctly capture responses of stomatal conductance to changing atmospheric CO₂, and thus can be used to test for stomatal acclimation to elevated CO₂. The reconciliation of the optimal and empirical approaches to modelling stomatal conductance is important for global change biology because it provides a simple theoretical framework for analyzing, and simulating, the coupling between carbon and water cycles under environmental change.     

A hydromechanical and biochemical model of stomatal conductance

A mathematical model of stomatal conductance is presented. It is based on whole‐plant and epidermal hydromechanics, and on two hypotheses: (1) the osmotic gradient across guard cell membranes is proportional to the concentration of ATP in the guard cells; and (2) the osmotic gradient that can be sustained per unit of ATP is proportional to the turgor pressure of adjacent epidermal cells. In the present study, guard cell [ATP] is calculated using a previously published model that is based on a widely used biochemical model of C₃ mesophyll photosynthesis. The conductance model for Vicia faba L. is parameterized and tested As with most other stomatal models, the present model correctly predicts the stomatal responses to variations in transpiration rate, irradiance and intercellular CO₂. Unlike most other models, however, this model can predict the transient stomatal opening often observed before conductance declines in response to decreases in humidity, soil water potential, or xylem conductance. The model also explicitly accommodates the mechanical advantage of the epidermis and correctly predicts that stomata are relatively insensitive to the ambient partial pressure of oxygen, as a result of the assumed dependence on ATP concentration.     

The effect of light on stomatal control of gas exchange in Douglas fir (Pseudotsuga menziesii) saplings

Summary Attached twigs of young Pseudotsuga menziesii (Mirb.) Franco plants were subjected to variations in irradaince. Stomatal responsiveness to irradiance, measured in an open type gas exchange system, varied seasonally. During the autumn and winter, stomatal conductance was relatively unresponsive to changes in irradiance, but during the summer stomatal conductance decreased in response to reduced irradiance. The summer stomatal response to irradiance was such that a nearly constant ratio of stomatal conductance to net photosynthesis was maintained as irradiance was varied. This caused intercellular CO₂ concentration (c _i) and water use efficiency (net CO₂ uptake/transpiration) to also remain relatively constant. At constant irradiance, stomatal conductance was relatively insensitive to experimentally-induced changes in c _i. This, and the observation that c _i remained relatively constant as irradiance was varied, suggest that changes in c _i played a minor role in mediating the stomatal response to light.The ecological significance of the seasonal changes in stomatal response to light is discussed.     

Non-uniform stomatal closure of hybrid poplar clones under light stress determined by scanning electron microscopy and modification of intercellular CO2 concentration

The stomatal distribution, non-uniform stomatal closure, stomatal conductance, and gas-exchange of several hybrid poplar clones under light stress were studied using scanning electron microscopy (SEM) and gas-exchange. Non-uniform stomatal closure was found under natural light stress by SEM, and there was a linear relationship between the stomatal aperture and stomatal conductance. We suggest a formula for modification of intercellular CO₂ concentration, which can restore consideration of stomatal factors leading to midday depression of photosynthesis in some cases. Received: 11 January 1999 / Accepted: 6 April 2000     

Effects of Nitrate Application on Amaranthus powellii Wats. : III. Optimal Allocation of Leaf Nitrogen for Photosynthesis and Stomatal Conductance

Optimal allocation of leaf nitrogen maximizes daily CO₂ assimilation for a given leaf nitrogen concentration. According to the hypothesis of optimization, this condition occurs when the partial derivative of assimilation rate with respect to leaf nitrogen concentration is constant. This hypothesis predicts a linear increase of assimilation rate with leaf nitrogen concentration under constant conditions. Plants of Amaranthus powellii Wats. were grown at 1, 5, 10, or 45 millimolar nitrate to obtain leaves with different nitrogen concentrations. Assimilation rate at 340 microbar CO₂/bar, stomatal conductance, CO₂- and light-saturated net photosynthetic rate, the initial slope of the CO₂ response of photosynthesis, ribulose-1,5′-bisphosphate carboxylase activity, and phosphoenolpyruvate carboxylase activity were linearly related to estimated or actual leaf nitrogen concentration. The data are consistent with the optimal use of leaf nitrogen. This hypothesis and the hypothesis of optimal stomatal conductance were combined to determine the relationship between conductance and leaf nitrogen concentration. The slope of conductance versus leaf nitrogen concentration was not significantly different than the slope predicted by the combination of the two hypotheses. Stomatal conductance was linearly related to leaf nitrogen in the field and the slope decreased with lower xylem pressure potentials in a manner consistent with the hypotheses. Finally, apparent maximum stomatal aperture of isolated abaxial epidermal strips was linearly related to leaf nitrogen suggesting stomatal conductance and assimilation rate are controlled in parallel by leaf nitrogen concentration or some factor correlated with leaf nitrogen.