scholarly journals Plant resistance to drought relies on early stomatal closure

2017 ◽  
Author(s):  
N Martin-StPaul ◽  
S Delzon ◽  
H Cochard

ABSTRACTPlant resistance to drought has long been thought to be associated with the ability to maintain transpiration and photosynthesis longer during drought, through the opening of stomata. This premise is at the root of most current framework used to assess drought impacts on land plants in vegetation models. We examined this premise by coupling a meta-analysis of functional traits of stomatal response to drought (i.e. the water potential causing stomatal closure, Ψclose) and embolism resistance (the water potential at the onset of embolism formation, Ψ12), with simulations from a soil-plant hydraulic model. We found that Ψclose and Ψ12 were equal (isometric) only for a restricted number of species, but as Ψ12 decreases, the departure from isometry increases, with stomatal closure occurring far before embolism occurs. For the most drought resistant species (Ψ12<-4.2 MPa), Ψclose was remarkably independent of embolism resistance and remained above −4.5 MPa, suggesting the existence of a restrictive boundary by which stomata closure must occur. This pattern was supported by model simulations. Indeed, coordinated decrease in both Ψclose and Ψ12 leads to unsuspected accelerated death under drought for embolism resistant species, in contradiction with observations from drought mortality experiments. Overall our results highlight that most species have similarity in stomatal behavior, and are highly conservative in terms of their water use during drought. The modelling framework presented here provides a baseline to simulate the temporal dynamic leading to mortality under drought by accounting for multiple, measurable traits.

1989 ◽  
Vol 16 (5) ◽  
pp. 429 ◽  
Author(s):  
IE Henson ◽  
CR Jensen ◽  
NC Turner

Changes in the content of endogenous abscisic acid (ABA) were followed in glasshouse experiments during stomatal closure induced by drought in leaves of lupin (Lupinus cosentinii Guss. cv. Eregulla) and wheat (Triticum aestivum L. cvv. Gamenya and Warigal), species which differ in stomatal sensitivity to changes in leaf water potential. Increases in bulk leaf ABA concentration were closely correlated with decreases in leaf conductance in both species. In lupin, substantial increases in ABA and decreases in conductance occurred over a very narrow range of leaf water potential. ABA concentrations in wheat leaves were highly negatively correlated with bulk leaf turgor, but there was no significant relationship between ABA and turgor in lupin. However, ABA accumulated progressively in the leaves of both species as soil water content decreased. Stomatal closure in lupin could be induced by supplying exogenous ABA to detached leaves via the transpiration stream at concentrations of 10-4 to 10-2 mol m-3 of (+)-ABA. Abaxial stomata closed more readily than those on the adaxial surface in response to both drought and applied ABA. Stomatal response to ABA was not affected by the presence of the cytokinin zeatin, and zeatin by itself had no effect on conductance. When treatments designed to reduce endogenous cytokinin concentrations were imposed (prolonged leaf detachment or prior drought), stomatal response to low concentrations of ABA was enhanced. However, such treatments did not significantly change the stomatal response to high ABA concentrations, nor affect the stomatal conductance of leaves supplied with water alone. It is concluded that drought-induced stomatal closure could be mediated by ABA in both wheat and lupin, despite the initially small change in leaf water status in the latter species.


2004 ◽  
Vol 16 (3) ◽  
pp. 155-161 ◽  
Author(s):  
Mara de Menezes de Assis Gomes ◽  
Ana Maria Magalhães Andrade Lagôa ◽  
Camilo Lázaro Medina ◽  
Eduardo Caruso Machado ◽  
Marcos Antônio Machado

Thirty-month-old 'Pêra' orange trees grafted on 'Rangpur' lemon trees grown in 100 L pots were submitted to water stress by the suspension of irrigation. CO2 assimilation (A), transpiration (E) and stomatal conductance (g s) values declined from the seventh day of stress, although the leaf water potential at 6:00 a.m. (psipd) and at 2:00 p.m. (psi2) began to decline from the fifth day of water deficiency. The CO2 intercellular concentration (Ci) of water-stressed plants increased from the seventh day, reaching a maximum concentration on the day of most severe stress. The carboxylation efficiency, as revealed by the ratio A/Ci was low on this day and did not show the same values of non-stressed plants even after ten days of rewatering. After five days of rewatering only psi pd and psi2 were similar to control plants while A, E and g s were still different. When psi2 decreases, there was a trend for increasing abscisic acid (ABA) concentration in the leaves. Similarly, stomatal conductance was found to decrease as a function of decreasing psi2. ABA accumulation and stomatal closure occurred when psi2 was lower than -1.0 MPa. Water stress in 'Pera´ orange trees increased abscisic acid content with consequent stomatal closure and decreased psi2 values.


2016 ◽  
Vol 3 ◽  
pp. e007 ◽  
Author(s):  
Jean-Christophe Domec ◽  
Sari Palmroth ◽  
Ram Oren

Silvicultural practices (e.g., nitrogen addition through fertilization) and environmental changes (e.g., elevated [CO2]) may alter needle structure, impacting mass and energy exchange between the biosphere and atmosphere through alteration of stomatal function. Hydraulic resistances in leaves, controlling the mass and energy exchanges, occur both in the xylem and in the flow paths across the mesophyll to evaporation sites, and therefore largely depends on the structure of the leaf. We used the Free-Air Carbon dioxide Enrichment (FACE) experiment, providing a unique setting for assessing the interaction effects of [CO2] and nitrogen (N) supply to examine how leaf morphological and anatomical characteristics control leaf hydraulic conductance (Kleaf) of loblolly pine (Pinus taeda L.) trees subjected to ambient or elevated (+200 ppmv) CO2 concentrations (CO2a and CO2e, respectively) and to soil nitrogen amendment (N). Our study revealed that CO2e decreased the number of tracheids per needle, and increased the distance from the xylem vascular bundle to the stomata cavities, perturbing the leaf hydraulic system. Both treatments induced a decrease in Kleaf, and CO2e also decreased leaf extravascular conductance (Kextravascular), the conductance to water flow from the xylem to the leaf-internal air space. Decline in Kleaf under CO2e was driven by the decline in Kextravascular, potentially due to longer path for water movement through the mesophyll, explaining the decline in stomatal conductance (gs) observed under CO2e. This suggests that the distance from vascular conduits to stomata sub-cavity was a major constraint of leaf water transport. Across treatments our results showed that needle vein conductivity was slightly more limited by the lumen than by the bordered-pits, the latter accounting for 30-45% of vein resistance. CO2e-induced reduction in Kleaf was also consistent with an increased resistance to xylem collapse due to thicker cell wall. In addition, stomatal closure corresponded to the water potential inducing a reduction in 50% of leaf vascular conductance (Kvascular) via xylem wall rupture. The water potential that was estimated to induce complete xylem wall collapse was related to the water potential at turgor loss. Our study provided a framework for understanding the interaction between CO2e and N availability in affecting leaf anatomy, and the mechanisms for the response of Kleaf to the treatments. These mechanisms can be incorporated into predictive models of gs, critical for estimating forest productivity in water limited environments in current and future climates and a landscape composed of sites of a range in soil N fertility. 


1984 ◽  
Vol 102 (2) ◽  
pp. 415-425 ◽  
Author(s):  
M. McGowan ◽  
P. Blanch ◽  
P. J. Gregory ◽  
D. Haycock

SummaryShoot and root growth and associated leaf and soil water potential relations were compared in three consecutive crops of winter wheat grown in the same field. Despite a profuse root system the crop grown in the second drought year (1976) failed to dry the soil as throughly as the crops in 1975 and 1977. Measurements of plant water potential showed that the restricted utilization of soil water reserves by this crop was associated with failure to make any significant osmotic adjustment, leading to premature loss of leaf turgor and stomatal closure. The implications of these results for models to estimate actual crop evaporation from values of potential evaporation are discussed.


2021 ◽  
Author(s):  
Fabian Wankmüller ◽  
Mohsen Zarebanadkouki ◽  
Andrea Carminati

&lt;p&gt;Predicting plant responses to drought is a long-standing research goal. Since stomata regulate gas-exchange between plants and the atmosphere, understanding their response to drought is fundamental. Current predictions of stomatal behavior during drought mainly rely on empirical models. These models may suit well to a specific set of plant traits and environmental growth conditions, but their predictive value is doubtful when atmospheric and soil conditions change. Stomatal optimization offers an alternative framework to predict stomatal regulation in response to drought for varying environmental conditions and plant traits. Models which apply this optimization principle posit that stomata maximize the carbon gain in relation to a penalty caused by water loss, such as xylem cavitation. Optimization models have the advantage of requiring a limited number of parameters and have been successfully used to predict stomatal response to drought for varying environmental conditions and species. However, a mechanism that enables stomata to optimally close in response to water limitations, and more precisely to a drop in the ability of the soil-plant continuum to sustain the transpiration demand, is not known. Here, we propose a model of stomatal regulation that is linked to abscisic acid (ABA) dynamics (production, degradation and transport) and that allows plants to avoid excessive drops in leaf water potential during soil drying and increasing vapor pressure deficit (VPD). The model assumes that: 1) stomatal conductance (g&lt;sub&gt;s&lt;/sub&gt;) decreases when ABA concentration close to the guard cells (C&lt;sub&gt;ABA&lt;/sub&gt;) increases; 2) C&lt;sub&gt;ABA&lt;/sub&gt; increases with decreasing leaf water potential (due to higher production); and 3) C&lt;sub&gt;ABA&lt;/sub&gt; decreases with increasing photosynthesis (e.g. due to faster degradation or transport to the phloem). Our model includes simulations of leaf water potential based on transpiration rate, soil water potential and variable hydraulic conductances of key elements (rhizosphere, root and xylem), and a function linking stomatal conductance to assimilation. It was tested for different soil properties and VPD. The model predicts that stomata close when the relation between assimilation and leaf water potential becomes nonlinear. In wet soil conditions and low VPD, when there is no water limitation, this nonlinearity is controlled by the relation between stomatal conductance and assimilation. In dry soil conditions, when the soil hydraulic conductivity limits the water supply, nonlinearity is controlled by the excessive drop of leaf water potential for increasing transpiration rates. The model predicts different relations between stomatal conductance and leaf water potential for varying soil properties and VPD. For instance, the closure of stomata is more abrupt in sandy soil, reflecting the steep decrease in hydraulic conductivity of sandy soils. In summary, our model results in an optimal behavior, in which stomatal closure avoids excessive (nonlinear) decrease in leaf water potential, similar to other stomatal optimization models. As based on ABA concentration which increases with decreasing leaf water potential but declines with assimilation, this model is a preliminary attempt to link optimization models to a physiological mechanism.&lt;/p&gt;


2019 ◽  
Vol 97 (9) ◽  
pp. 755-762 ◽  
Author(s):  
Michel J. Kaiser

Bottom trawling accounts for nearly a quarter of wild-capture seafood production, but it is associated with physical disturbance of the seabed leading to changes in benthic abundance, habitat structure, and biogeochemical processes. Understanding the processes of benthic depletion and recovery in relation to different types of fishing gears, and in different seabed types, is an important pre-requisite to inform appropriate management measures to limit or reduce the effects of trawling on the seabed. The combined approaches of meta-analysis and modelling that link fishing-gear penetration of the seabed to benthic depletion, and recovery to taxon longevity, have enabled the development of a modelling framework to estimate relative benthic status in areas subject to trawling. Such estimations are highly sensitive to the spatial resolution at which fishing footprint (trawl track) data are aggregated, and this leads to overinflated estimates of fishing impacts on benthos when coarse-level aggregation is applied. These approaches present a framework into which other “sustainability” criteria can be added, e.g., the consideration of carbon footprints of fishing activities.


1998 ◽  
Vol 25 (3) ◽  
pp. 353 ◽  
Author(s):  
C.R. Jensen ◽  
V.O. Mogensen ◽  
H.-H. Poulsen ◽  
I.E. Henson ◽  
S. Aagot ◽  
...  

Drought responses in leaves of lupin (Lupinus angustifolius L., cv. Polonez) were investigated in plants grown in lysimeters either in a sand or in a loam soil in the field. Abscisic acid (ABA) content, water potential (ψl) and conductance to water vapour (gH2O) were determined in leaves of both irrigated plants and in plants exposed to gradual soil drying. Amorning-peak of leaf ABA content was found in both fully watered and droughted plants. During soil drying which, on both soils types, only decreased soil water potential of the upper soil layers, mid-day leaf ABA content increased relative to that in fully irrigated plants before any appreciable decreases occurred in ψl. In the part of the soil profile from which water was taken up (0–60 cm depth), gH2O decreased when the relative available soil water content (RASW) on sand was below 12% and RASW on loam, below 30%. At this point the average soil water matric potential (ψsoil) on sand was less than –0.13 MPa and the fraction of roots in ‘wet’ soil was 0.12, while on loam, the fraction of roots in ‘wet’ soil was 0.44 while y soil was similar to that on sand. A critical leaf ABA content of 300–400 ng/g FW was associated with the onset of stomatal closure on both soil types. We suggest that the initial stomatal closure is controlled by ABA which originates from the roots where its production is closely related to ψsoiland the water potential of the root surface and that ψsoil is a more important parameter than RASW or the fraction of roots in ‘wet’ soil for affecting leaf gas exchange. Further drying on both soils led to further increases in leaf ABA and declines in ψl and gH2O. In order to gain further insight, experiments should be designed which combine signalling studies with simulation studies, which take account of soil water potential, root contact area and water flux when calculating the water status at the root surface in the soil-plant-atmosphere-continuum.


1989 ◽  
Vol 16 (5) ◽  
pp. 415 ◽  
Author(s):  
CR Jensen ◽  
IE Henson ◽  
NC Turner

Plants of Lupinus cosentinii Guss. cv. Eregulla were grown in a sandy soil in large containers in a glasshouse and exposed to drought by withholding water. Under these conditions stomatal closure had previously been shown to be initiated before a significant reduction in leaf water potential was detected. In the experiments reported here, no significant changes were found in water potential or turgor pressure of roots or leaves when a small reduction in soil water potential was induced which led to a 60% reduction in leaf conductance. The decrease in leaf conductance and root water uptake closely paralleled the fraction of roots in wet soil. By applying observed data of soil water and root characteristics, and root water uptake for whole pots in a single-root model, the average water potential at the root surface was calculated. Potential differences for water transport in the soil-plant system, and the resistances to water flow were estimated using the 'Ohm's Law' analogy for water transport. Soil resistance was negligible or minor, whereas the root resistance accounted for 61-72% and the shoot resistance accounted for about 30% of the total resistance. The validity of the measurements and calculations is discussed and the possible role of root- to-shoot communication raised.


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