scholarly journals Declining soil-root hydraulic conductance drives stomatal closure of tomato under drought 

Author(s):  
Mohanned Abdalla ◽  
Andrea Carminati ◽  
Gaochao Cai ◽  
Mathieu Javaux ◽  
Mutez Ahmed

<p>The fundamental question as to what triggers stomatal closure during soil drying remains contentious. Thus, we urgently need to improve our understanding of stomatal response to water deficits in soil and atmosphere.<strong> </strong>Here, we investigated the role of soil-plant hydraulic conductance (K<sub>sp</sub>) on transpiration (E) and stomata regulation. We used a root pressure chamber to measure the relation between E, leaf xylem water potential (ψ<sub>leaf-x</sub>) and soil water potential (ψ<sub>soil</sub>) in tomato. Additional measurements of ψ<sub>leaf-x</sub> were performed with unpressurized plants. A soil-plant hydraulic model was used to simulate E(ψ<sub>leaf-x</sub>) for decreasing ψ<sub>soil</sub>. In wet soils, E(ψ<sub>leaf-x</sub>) had a constant slope while in dry soils the slope decreased, with ψ<sub>leaf-x</sub> rapidly and nonlinearly decreasing for moderate increases in E. The ψ<sub>leaf-x</sub> measured in pressurized and unpressurized plants matched well, which indicates that the shoot hydraulic conductance did not decrease during soil drying and that the decrease in K<sub>sp</sub> is caused by a decrease in soil-root conductance. The decrease of E matched well the onset of hydraulic nonlinearity. Our findings demonstrate that stomatal closure prevents the drop in ψ<sub>leaf-x</sub> caused by a decrease in K<sub>sp</sub> and elucidate a strong correlation between stomatal regulation and belowground hydraulic limitation.</p>

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.


2021 ◽  
Author(s):  
Andrea Carminati ◽  
Mathieu Javaux

<p>There is increasing need for mechanistic and predictive models of transpiration and stomatal response to drought. Global measurements of transpiration showed that the decrease in soil moisture is a primary constrain on transpiration. Additionally, a recent meta-analysis indicated that stomatal closure is explained by the loss in soil hydraulic conductivity, more than that of the xylem. Despite these evidences on the role of soil drying as a key driver of transpiration reduction, the mechanisms by which soil drying impacts transpiration, including the effect of different soil hydraulic properties, are not fully understood.</p><p>Here, we propose that stomata regulate transpiration in such a way that the relation between transpiration and the difference in water potential between soil and leaves remains linear during soil drying and increasing vapor pressure deficit (VPD). The onset of hydraulic nonlinearity sets the maximum stomatal conductance at a given soil water potential and VPD. The resulting trajectory of the stomatal conductance for varying soil water potentials and VPD depends on soil and plant hydraulics, with the soil hydraulic conductivity and root length being the most sensitive parameters.</p><p>From this hydraulic framework it follows that stomatal closure is not simply a function of soil moisture, soil water potential or leaf water potential. Instead, it depends on transpiration demand and soil-plant hydraulics in a predictable way. The proposed concept allows to predict transpiration reductions during drought with a limited number of parameters: transpiration demand, plant hydraulic conductivity, soil hydraulic conductivity and active root length. In conclusion, this framework highlights the role of the soil hydraulic conductivity as primary constrain on transpiration, and thus on stomatal conductance and photosynthesis.</p>


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.


1985 ◽  
Vol 15 (1) ◽  
pp. 185-188 ◽  
Author(s):  
T. M. Ballard ◽  
M. G. Dosskey

Needle water potential in western and mountain hemlock falls as the soil dries, but under our experimental conditions, it remained stable in Douglas-fir. Resistance to water flow from soil to foliage is higher for the hemlocks and increases more steeply as the soil dries. These findings physically account for the observation that water uptake is reduced relatively more for the hemlocks than for Douglas-fir, as soil water potential declines.


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.


2020 ◽  
Vol 447 (1-2) ◽  
pp. 565-578 ◽  
Author(s):  
Gaochao Cai ◽  
Mutez Ali Ahmed ◽  
Michaela A. Dippold ◽  
Mohsen Zarebanadkouki ◽  
Andrea Carminati

1989 ◽  
Vol 16 (3) ◽  
pp. 241 ◽  
Author(s):  
NZ Saliendra ◽  
FC Meinzer

Stomatal conductance, leaf and soil water status, transpiration, and apparent root hydraulic conductance were measured during soil drying cycles for three sugarcane cultivars growing in containers in a greenhouse. At high soil moisture, transpiration and apparent root hydraulic conductance differed considerably among cultivars and were positively correlated, whereas leaf water potential was similar among cultivars. In drying soil, stomatal and apparent root hydraulic conductance approached zero over a narrow (0.1 MPa) range of soil water suction. Leaf water potential remained nearly constant during soil drying because the vapor phase conductance of the leaves and the apparent liquid phase conductance of the root system declined in parallel. The decline in apparent root hydraulic conductance with soil drying was manifested as a large increase in the hydrostatic pressure gradient between the soil and the root xylem. These results suggested that control of stomatal conductance in sugarcane plants exposed to drying soil was exerted primarily at the root rather than at the leaf level.


Botany ◽  
2009 ◽  
Vol 87 (1) ◽  
pp. 10-15 ◽  
Author(s):  
G. Glatzel ◽  
B. W. Geils

Mistletoes are highly specialized perennial flowering plants adapted to parasitic life on aerial parts of their hosts. In our discussion on the physiological interactions between parasite and host, we focus on water relations, mineral nutrition, and the effect of host vigour. When host photosynthesis is greatest, the xylem water potential of the host is most negative. To maintain a flux gradient and avoid stomatal closure and wilting, the mistletoe must tolerate a more negative water potential than the host. Succulent leaves enhance water storage and allow mistletoes to rehydrate before their hosts rehydrate. Mistletoe infections may disrupt the host stomatal control system, causing early and oscillating closure of host stomata, thereby diminishing host photosynthetic gain. Mistletoes lack the active uptake of minerals of a typical plant root system and rely upon the haustorium to connect with the host for the essentially one-way flow of photosynthates and nutrients from host to parasite. Modest growth rates, tolerance, succulence, and rapid leaf turnover are some means by which mistletoes avoid mineral deficiency or excess. We propose high concentrations of some mobile elements in the mistletoe by comparison with the host result not from active uptake, but from the inevitable accumulation by a parasite that utilizes host phloem sap. The relationship between host condition and mistletoe performance varies by situation and over time. In some cases, the host can outgrow the mistletoe, but favorable host status can also accelerate mistletoe growth. A better understanding of the mistletoe–host interaction can be utilized in improved management of infested forest plantations for resource production as well as for conservation of biodiversity and endangered species.


Sign in / Sign up

Export Citation Format

Share Document