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Stomatal Response (stomatal + response)
Selected AbstractsStomatal responses to humidity and temperature in darknessPLANT CELL & ENVIRONMENT, Issue 7 2010KEITH A. MOTT ABSTRACT Stomatal responses to leaf temperature (Tl) and to the mole fractions of water vapour in the ambient air (wa) and the leaf intercellular air spaces (wi) were determined in darkness to remove the potential effects of changes in photosynthesis and intercellular CO2 concentration. Both the steady-state and kinetic responses of stomatal conductance (gs) to wa in darkness were found to be indistinguishable from those in the light. gs showed a steep response to the difference (,w) between wa and wi when wa was varied. The response was much less steep when wi was varied. Although stomatal apertures responded steeply to Tl when ,w was held constant at 17 mmol mol,1, the response was much less steep when ,w was held constant at about zero. Similar results were obtained in the light for ,w = 15 mmol mol,1 and ,w , 0 mmol mol,1. These results are discussed in the context of mechanisms for the stomatal response to humidity. [source] Stomatal responses to CO2 during a diel Crassulacean acid metabolism cycle in Kalanchoe daigremontiana and Kalanchoe pinnataPLANT CELL & ENVIRONMENT, Issue 5 2009SUSANNE VON CAEMMERER ABSTRACT To investigate the diurnal variation of stomatal sensitivity to CO2, stomatal response to a 30 min pulse of low CO2 was measured four times during a 24 h time-course in two Crassulacean acid metabolism (CAM) species Kalanchoe daigremontiana and Kalanchoe pinnata, which vary in the degree of succulence, and hence, expression and commitment to CAM. In both species, stomata opened in response to a reduction in pCO2 in the dark and in the latter half of the light period, and thus in CAM species, chloroplast photosynthesis is not required for the stomatal response to low pCO2. Stomata did not respond to a decreased pCO2 in K. daigremontiana in the light when stomata were closed, even when the supply of internal CO2 was experimentally reduced. We conclude that stomatal closure during phase III is not solely mediated by high internal pCO2, and suggest that in CAM species the diurnal variability in the responsiveness of stomata to pCO2 could be explained by hypothesizing the existence of a single CO2 sensor which interacts with other signalling pathways. When not perturbed by low pCO2, CO2 assimilation rate and stomatal conductance were correlated both in the light and in the dark in both species. [source] Influences of meteorological and vegetational factors on the partitioning of the energy of a rice paddy fieldHYDROLOGICAL PROCESSES, Issue 8 2005Hiroki Oue Abstract Observations made in a paddy field were analysed to show the influences of meteorological and vegetational factors on the crop's energy budget. Energy budget in the paddy field was characterized by the major partitioning to latent heat flux LE and by the negative Bowen ratio B mostly in the afternoon. Canopy resistance rc, estimated with the Penman,Monteith equation, was related to the influences of solar radiation SR, vapour pressure deficit VPD and plant height. The results demonstrated that rc could not directly account for B but that critical canopy resistance rcc, defined as the canopy resistance when B = 0, could be used to standardize rc, and that rc , rcc proved to be a good parameter to account for B. Influences of bulk stomatal response on energy partitioning were assessed as follows: the Bowen ratio dropped below zero, while the bulk stomatal aperture dwindled with the increase of VPD. In addition, stomata of a big leaf acted to promote the partitioning to LE against the rise of SR in the condition of higher VPD. Copyright © 2004 John Wiley & Sons, Ltd. [source] Biomass and leaf-level gas exchange characteristics of three African savanna C4 grass species under optimum growth conditionsAFRICAN JOURNAL OF ECOLOGY, Issue 4 2009K. B. Mantlana Abstract C4 savanna grass species, Digitaria eriantha, Eragrostis lehmanniana and Panicum repens, were grown under optimum growth conditions with the aim of characterizing their above- and below-ground biomass allocation and the response of their gas exchange to changes in light intensity, CO2 concentration and leaf-to-air vapour pressure deficit gradient (Dl). Digitaria eriantha showed the largest above- and below-ground biomass, high efficiency in carbon gain under light-limiting conditions, high water use efficiency (WUE) and strong stomatal sensitivity to Dl (P = 0.002; r2 = 0.5). Panicum repens had a high aboveground biomass and attained high light saturated photosynthetic rates (Asat, 47 ,mol m,2 s,1), stomatal conductance, (gsat, 0.25 mol m,2 s,1) at relatively high WUE. Eragrostis lehmanniana had almost half the biomass of other species, and had similar Asat and gsat but were attained at lower WUE than the other species. This species also showed the weakest stomatal response to Dl (P = 0.19, r2 = 0. 1). The potential ecological significance of the contrasting patterns of biomass allocation and variations in gas exchange parameters among the species are discussed. Résumé On a fait pousser des espèces herbeuses de savane de type C4, Digitaria eriantha, Eragrostis lehmanniana et Panicum repens, dans des conditions optimales dans le but de caractériser l'allocation de leur biomasse aérienne et racinaire et la réponse de leur échange gazeux à des changements d'intensité de la lumière, de concentrations de CO2, et à un gradient déficitaire (Dl) de pression de vapeur feuille-air. D. eriantha montrait la plus grande biomasse aérienne et racinaire, une grande efficience de l'assimilation de carbone dans des conditions de luminosité limitée, une grande efficience d'utilisation de l'eau (WUE) et une forte sensibilité des stomates à Dl (P = 0,002; r2 = 0,5). P. repens avait une grande biomasse aérienne et atteignait des taux photosynthétiques élevés en lumière saturée (Asat, 47 ,mol m,2 s,1), et une conductance stomatique (gsat 0.25 mol m,2 s,1) à une WUE relativement élevée. E. lehmanniana avait une biomasse qui était presque la moitié de celle des autres espèces et avait un Asat et un gsat similaires mais qui étaient atteints à une WUE plus basse que les autres espèces. Cette espèce montrait aussi la plus faible réponse stomatique àDl (P = 0,19, r2 = 0,1). L'on discute de la signification écologique potentielle de ces schémas contrastés d'allocations de biomasse et des variations des paramètres des échanges gazeux entre les espèces. [source] Abscisic Acid-mediated Epigenetic Processes in Plant Development and Stress ResponsesJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 10 2008Viswanathan Chinnusamy Abstract Abscisic acid (ABA) regulates diverse plant processes, growth and development under non-stress conditions and plays a pivotal role in abiotic stress tolerance. Although ABA-regulated genetic processes are well known, recent discoveries reveal that epigenetic processes are an integral part of ABA-regulated processes. Epigenetic mechanisms, namely, histone modifications and cytosine DNA methylation-induced modification of genome give rise to epigenomes, which add diversity and complexity to the genome of organisms. Histone monoubiquitination appears to regulate ABA levels in developing seeds through histone H2B monoubiquitination. ABA and H2B ubiquitination dependent chromatin remodeling regulate seed dormancy. Transcription factor networks necessary for seed maturation are repressed by histone deacetylases (HDACs)-dependent and PICKLE chromatin remodeling complexes (CRCs), whereas ABA induces the expression of these genes directly or through repression of HDACs. Abiotic stress-induced ABA regulates stomatal response and stress-responsive gene expression through HDACs and HOS15-dependent histone deacetylation, as well as through the ATP-dependent SWITCH/SUCROSE NONFERMENTING CRC. ABA also probably regulates the abiotic stress response through DNA methylation and short interfering RNA pathways. Further studies on ABA-regulated epigenome will be of immense use to understand the plant development, stress adaptation and stress memory. [source] Stomatal responses to humidity and temperature in darknessPLANT CELL & ENVIRONMENT, Issue 7 2010KEITH A. MOTT ABSTRACT Stomatal responses to leaf temperature (Tl) and to the mole fractions of water vapour in the ambient air (wa) and the leaf intercellular air spaces (wi) were determined in darkness to remove the potential effects of changes in photosynthesis and intercellular CO2 concentration. Both the steady-state and kinetic responses of stomatal conductance (gs) to wa in darkness were found to be indistinguishable from those in the light. gs showed a steep response to the difference (,w) between wa and wi when wa was varied. The response was much less steep when wi was varied. Although stomatal apertures responded steeply to Tl when ,w was held constant at 17 mmol mol,1, the response was much less steep when ,w was held constant at about zero. Similar results were obtained in the light for ,w = 15 mmol mol,1 and ,w , 0 mmol mol,1. These results are discussed in the context of mechanisms for the stomatal response to humidity. [source] Stomatal responses to CO2 during a diel Crassulacean acid metabolism cycle in Kalanchoe daigremontiana and Kalanchoe pinnataPLANT CELL & ENVIRONMENT, Issue 5 2009SUSANNE VON CAEMMERER ABSTRACT To investigate the diurnal variation of stomatal sensitivity to CO2, stomatal response to a 30 min pulse of low CO2 was measured four times during a 24 h time-course in two Crassulacean acid metabolism (CAM) species Kalanchoe daigremontiana and Kalanchoe pinnata, which vary in the degree of succulence, and hence, expression and commitment to CAM. In both species, stomata opened in response to a reduction in pCO2 in the dark and in the latter half of the light period, and thus in CAM species, chloroplast photosynthesis is not required for the stomatal response to low pCO2. Stomata did not respond to a decreased pCO2 in K. daigremontiana in the light when stomata were closed, even when the supply of internal CO2 was experimentally reduced. We conclude that stomatal closure during phase III is not solely mediated by high internal pCO2, and suggest that in CAM species the diurnal variability in the responsiveness of stomata to pCO2 could be explained by hypothesizing the existence of a single CO2 sensor which interacts with other signalling pathways. When not perturbed by low pCO2, CO2 assimilation rate and stomatal conductance were correlated both in the light and in the dark in both species. [source] Relations between stomatal closure, leaf turgor and xylem vulnerability in eight tropical dry forest treesPLANT CELL & ENVIRONMENT, Issue 3 2003T. J. BRODRIBB ABSTRACT This study examined the linkage between xylem vulnerability, stomatal response to leaf water potential (,L), and loss of leaf turgor in eight species of seasonally dry tropical forest trees. In order to maximize the potential variation in these traits species that exhibit a range of leaf habits and phenologies were selected. It was found that in all species stomatal conductance was responsive to ,L over a narrow range of water potentials, and that ,L inducing 50% stomatal closure was correlated with both the ,L inducing a 20% loss of xylem hydraulic conductivity and leaf water potential at turgor loss in all species. In contrast, there was no correlation between the water potential causing a 50% loss of conductivity in the stem xylem, and the water potential at stomatal closure (,SC) amongst species. It was concluded that although both leaf and xylem characters are correlated with the response of stomata to ,L, there is considerable flexibility in this linkage. The range of responses is discussed in terms of the differing leaf-loss strategies exhibited by these species. [source] The Ball,Berry,Leuning and Tardieu,Davies stomatal models: synthesis and extension within a spatially aggregated picture of guard cell functionPLANT CELL & ENVIRONMENT, Issue 11 2002R. C. Dewar Abstract A new model of stomatal conductance is proposed which combines the essential features of the Ball,Berry,Leuning (BBL) and Tardieu,Davies (TD) models within a simple spatially aggregated picture of guard cell function. The model thus provides a coherent description of stomatal responses to both air and soil environments. The model also presents some novel features not included in either the BBL or TD models: stomatal sensing of intercellular (rather than leaf surface) CO2 concentration; an explanation of all three observed regimes (A, B and C) of the stomatal response to air humidity (Monteith Plant, Cell and Environment 18, 357,364, 1995); incorporation of xylem embolism; and maintenance of hydraulic homeostasis by combined hydraulic and chemical signalling in leaves (in which leaf epidermal hydraulic conductivity plays a key role). Significantly, maintenance of hydraulic homeostasis in the model does not require a direct feedback signal from xylem embolism, the predicted minimum leaf water potential being independent of xylem hydraulic conductivity. It is suggested that stomatal regulation through combined hydraulic and chemical signalling in leaves and/or roots provides a general mechanism enabling plants to maintain their water potentials above a minimum value. Natural selection of the key stomatal parameters would then set the minimum potential to a specific value determined by the most vulnerable plant process under water stress (e.g. cell growth, protein synthesis or xylem cavitation), depending on species and growth conditions. [source] Does engineering abscisic acid biosynthesis in Nicotiana plumbaginifolia modify stomatal response to drought?PLANT CELL & ENVIRONMENT, Issue 5 2001C. Borel ABSTRACT 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. [source] RATP: a model for simulating the spatial distribution of radiation absorption, transpiration and photosynthesis within canopies: application to an isolated tree crownPLANT CELL & ENVIRONMENT, Issue 4 2001H. Sinoquet ABSTRACT The model RATP (radiation absorption, transpiration and photosynthesis) is presented. The model was designed to simulate the spatial distribution of radiation and leaf-gas exchanges within vegetation canopies as a function of canopy structure, canopy microclimate within the canopy and physical and physiological leaf properties. The model uses a three-dimensional (3D) representation of the canopy (i.e. an array of 3D cells, each characterized by a leaf area density). Radiation transfer is computed by a turbid medium analogy, transpiration by the leaf energy budget approach, and photosynthesis by the Farquhar model, each applied for sunlit and shaded leaves at the individual 3D cell-scale. The model typically operates at a 20,30 min time step. The RATP model was applied to an isolated, 20-year-old walnut tree grown in the field. The spatial distribution of wind speed, stomatal response to environmental variables, and light acclimation of leaf photosynthetic properties were taken into account. Model outputs were compared with data acquired in the field. The model was shown to simulate satisfactorily the intracrown distribution of radiation regime, transpiration and photosynthetic rates, at shoot or branch scales. [source] Modulation of Root Signals in Relation to Stomatal Sensitivity to Root-sourced Abscisic Acid in Drought-affected PlantsJOURNAL OF INTEGRATIVE PLANT BIOLOGY, Issue 10 2007Huibo Ren Abstract Stomatal sensitivity to root signals induced by soil drying may vary between environments and plant species. This is likely to be a result of the interactions and modulations among root signals. As a stress signal, abscisic acid (ABA) plays a central role in root to shoot signaling. pH and hydraulic signals may interact with ABA signals and thus, jointly regulate stomatal responses to changed soil water status. pH itself can be modified by several factors, among which the chemical compositions in the xylem stream and the live cells surrounding the vessels play crucial roles. In addition to the xylem pH, more attention should be paid to the direct modulation of leaf apoplastic pH, because many chemical compositions might strongly modify the leaf apoplastic pH while having no significant effect on the xylem pH. The direct modulation of the ABA signal intensity may be more important for the regulation of stomatal responses to soil drying than the ABA signal per se. The ABA signal is also regulated by the ABA catabolism and the supply of precursors to the roots if a sustained root to shoot communication of soil drying operates at the whole plant level. More importantly, ABA catabolism could play crucial roles in the determination of the fate of the ABA signal and thereby control the stomatal behavior of the root-sourced ABA signal. [source] Diurnal and seasonal variations in stomatal conductance of rice at elevated atmospheric CO2 under fully open-air conditionsPLANT CELL & ENVIRONMENT, Issue 3 2010HIROYUKI SHIMONO ABSTRACT Understanding of leaf stomatal responses to the atmospheric CO2 concentration, [CO2], is essential for accurate prediction of plant water use under future climates. However, limited information is available for the diurnal and seasonal changes in stomatal conductance (gs) under elevated [CO2]. We examined the factors responsible for variations in gs under elevated [CO2] with three rice cultivars grown in an open-field environment under flooded conditions during two growing seasons (a total of 2140 individual measurements). Conductance of all cultivars was generally higher in the morning and around noon than in the afternoon, and elevated [CO2] decreased gs by up to 64% over the 2 years (significantly on 26 out of 38 measurement days), with a mean gs decrease of 23%. We plotted the gs variations against three parameters from the Ball-Berry model and two revised versions of the model, and all parameters explained the gs variations well at each [CO2] in the morning and around noon (R2 > 0.68), but could not explain these variations in the afternoon (R2 < 0.33). The present results provide an important basis for modelling future water use in rice production. [source] Leaf stomatal responses to vapour pressure deficit under current and CO2 -enriched atmosphere explained by the economics of gas exchangePLANT CELL & ENVIRONMENT, Issue 8 2009GABRIEL G. KATUL ABSTRACT Using the economics of gas exchange, early studies derived an expression of stomatal conductance (g) assuming that water cost per unit carbon is constant as the daily loss of water in transpiration (fe) is minimized for a given gain in photosynthesis (fc). Other studies reached identical results, yet assumed different forms for the underlying functions and defined the daily cost parameter as carbon cost per unit water. We demonstrated that the solution can be recovered when optimization is formulated at time scales commensurate with the response time of g to environmental stimuli. The optimization theory produced three emergent gas exchange responses that are consistent with observed behaviour: (1) the sensitivity of g to vapour pressure deficit (D) is similar to that obtained from a previous synthesis of more than 40 species showing g to scale as 1 , m log(D), where m ? [0.5,0.6], (2) the theory is consistent with the onset of an apparent ,feed-forward' mechanism in g, and (3) the emergent non-linear relationship between the ratio of intercellular to atmospheric [CO2] (ci/ca) and D agrees with the results available on this response. We extended the theory to diagnosing experimental results on the sensitivity of g to D under varying ca. [source] The Ball,Berry,Leuning and Tardieu,Davies stomatal models: synthesis and extension within a spatially aggregated picture of guard cell functionPLANT CELL & ENVIRONMENT, Issue 11 2002R. C. Dewar Abstract A new model of stomatal conductance is proposed which combines the essential features of the Ball,Berry,Leuning (BBL) and Tardieu,Davies (TD) models within a simple spatially aggregated picture of guard cell function. The model thus provides a coherent description of stomatal responses to both air and soil environments. The model also presents some novel features not included in either the BBL or TD models: stomatal sensing of intercellular (rather than leaf surface) CO2 concentration; an explanation of all three observed regimes (A, B and C) of the stomatal response to air humidity (Monteith Plant, Cell and Environment 18, 357,364, 1995); incorporation of xylem embolism; and maintenance of hydraulic homeostasis by combined hydraulic and chemical signalling in leaves (in which leaf epidermal hydraulic conductivity plays a key role). Significantly, maintenance of hydraulic homeostasis in the model does not require a direct feedback signal from xylem embolism, the predicted minimum leaf water potential being independent of xylem hydraulic conductivity. It is suggested that stomatal regulation through combined hydraulic and chemical signalling in leaves and/or roots provides a general mechanism enabling plants to maintain their water potentials above a minimum value. Natural selection of the key stomatal parameters would then set the minimum potential to a specific value determined by the most vulnerable plant process under water stress (e.g. cell growth, protein synthesis or xylem cavitation), depending on species and growth conditions. [source] | ||||||||||