| P50 | author | Antonio Diaz-Espejo | Q41237779 |
| | Virginia Hernandez-Santana | Q57315723 |
| | Thomas N. Buckley | Q57412703 |
| | Celia M Rodriguez-Dominguez | Q58330143 |
| | Sebastià Martorell | Q124419506 |
| P2093 | author name string | Alfonso de Cires | |
| | Gregorio Egea | |
| P2860 | cites work | Unraveling the effects of plant hydraulics on stomatal closure during water stress in walnut | Q24549644 |
| | Mechanisms of abscisic acid-mediated control of stomatal aperture | Q28604202 |
| | The Interpretation of the Variations in Leaf Water Potential and Stomatal Conductance Found in Canopies in the Field | Q30054673 |
| | The mechanical diversity of stomata and its significance in gas-exchange control | Q33264048 |
| | A biochemical model of photosynthetic CO2 assimilation in leaves of C 3 species. | Q34389800 |
| | FRET-based reporters for the direct visualization of abscisic acid concentration changes and distribution in Arabidopsis | Q34415432 |
| | Guard cell signaling. | Q34465407 |
| | The role of stomata in sensing and driving environmental change | Q35204084 |
| | Diffusive and metabolic limitations to photosynthesis under drought and salinity in C(3) plants. | Q35773272 |
| | The control of stomata by water balance. | Q36283871 |
| | The dynamics of embolism refilling in abscisic acid (ABA)-deficient tomato plants. | Q36589901 |
| | Chemical root to shoot signaling under drought. | Q37158163 |
| | Opinion: stomatal responses to light and CO(2) depend on the mesophyll | Q37559874 |
| | Opinion: the red-light response of stomatal movement is sensed by the redox state of the photosynthetic electron transport chain | Q38088659 |
| | Mesophyll photosynthesis and guard cell metabolism impacts on stomatal behaviour | Q38235471 |
| | Modelling the coordination of the controls of stomatal aperture, transpiration, leaf growth, and abscisic acid: update and extension of the Tardieu-Davies model. | Q38377463 |
| | Stomatal closure with soil water depletion not associated with changes in Bulk leaf water status | Q38896731 |
| | Abscisic acid mediates a divergence in the drought response of two conifers. | Q38922021 |
| | Hydraulic failure defines the recovery and point of death in water-stressed conifers | Q38922029 |
| | Generation of active pools of abscisic acid revealed by in vivo imaging of water-stressed Arabidopsis | Q38946590 |
| | Is xylem cavitation resistance a relevant criterion for screening drought resistance among Prunus species? | Q38949396 |
| | Seasonal evolution of diffusional limitations and photosynthetic capacity in olive under drought | Q38972749 |
| | Modeling photosynthesis in olive leaves under drought conditions | Q38981094 |
| | Passive and active stomatal control: either or both? | Q39010763 |
| | Guard cell volume and pressure measured concurrently by confocal microscopy and the cell pressure probe. | Q39010787 |
| | Root ABA Accumulation in Long-Term Water-Stressed Plants is Sustained by Hormone Transport from Aerial Organs. | Q39213169 |
| | Plasticity of vulnerability to leaf hydraulic dysfunction during acclimation to drought in grapevines: an osmotic-mediated process. | Q39220348 |
| | The dual effect of abscisic acid on stomata | Q39337145 |
| | Canopy stomatal conductance and xylem sap abscisic acid (ABA) in mature Scots pine during a gradually imposed drought | Q39350424 |
| | Water deficits and hydraulic limits to leaf water supply | Q39482891 |
| | Stomatal response to abscisic Acid is a function of current plant water status. | Q39511675 |
| | Role of hydraulic and chemical signals in leaves, stems and roots in the stomatal behaviour of olive trees under water stress and recovery conditions | Q39530328 |
| | Re-examining the role of ABA as the primary long-distance signal produced by water-stressed roots. | Q42148136 |
| | Contrasting physiological effects of partial root zone drying in field-grown grapevine (Vitis vinifera L. cv. Monastrell) according to total soil water availability | Q42239426 |
| | Abscisic acid signalling when soil moisture is heterogeneous: decreased photoperiod sap flow from drying roots limits abscisic acid export to the shoots | Q46571685 |
| | Stomatal responses to vapour pressure deficit are regulated by high speed gene expression in angiosperms. | Q46672281 |
| | Stomatal responses to light and leaf-air water vapor pressure difference show similar kinetics in sugarcane and soybean | Q46854878 |
| | Partitioning changes in photosynthetic rate into contributions from different variables. | Q51031363 |
| | A new, vapour‐phase mechanism for stomatal responses to humidity and temperature | Q51653251 |
| | Temperature response of mesophyll conductance. Implications for the determination of Rubisco enzyme kinetics and for limitations to photosynthesis in vivo. | Q55036263 |
| | The Stomatal Response to Reduced Relative Humidity Requires Guard Cell-Autonomous ABA Synthesis | Q56027345 |
| | The Ball-Berry-Leuning and Tardieu-Davies stomatal models: synthesis and extension within a spatially aggregated picture of guard cell function | Q57311823 |
| | Rapid Changes in Transpiration in Plants | Q59098215 |
| | Steps toward an improvement in process-based models of water use by fruit trees: A case study in olive | Q59259893 |
| P433 | issue | 9 | |
| P921 | main subject | drought | Q43059 |
| P304 | page(s) | 2014-2026 | |
| P577 | publication date | 2016-06-02 | |
| P1433 | published in | Plant, Cell and Environment | Q15766307 |
| P1476 | title | Most stomatal closure in woody species under moderate drought can be explained by stomatal responses to leaf turgor | |
| P478 | volume | 39 | |