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Signal coordination before, during and after stomatal closure in response to drought stress
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Outgoing claims: the papers this work cites, builds on, or argues with.
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A dynamical system perspective on plant hydraulic failure
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Xylem Structure and the Ascent of Sap
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Xylem Structure and the Ascent of Sap
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inferredcites →https://doi.org/10.1007/bf00390306openalex-snapshot
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inferredcites →https://doi.org/10.1007/s004680100095openalex-snapshot
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inferredcites →https://doi.org/10.1007/s11183-005-0038-1openalex-snapshot
Calcium signaling system in plants
inferredcites →https://doi.org/10.1016/j.envexpbot.2011.12.004openalex-snapshot
Both ozone exposure and soil water stress are able to induce stomatal sluggishness
inferredcites →https://doi.org/10.1016/j.envpol.2004.09.011openalex-snapshot
Ozone slows stomatal response to light and leaf wounding in a Mediterranean evergreen broadleaf, Arbutus unedo
inferredcites →https://doi.org/10.1016/j.jtbi.2009.03.039openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.pbi.2013.02.011openalex-snapshot
Hydraulic signals in long-distance signaling
inferredcites →https://doi.org/10.1016/j.pbi.2015.10.010openalex-snapshot
Mechanisms of abscisic acid-mediated control of stomatal aperture
inferredcites →https://doi.org/10.1016/j.tplants.2008.04.003openalex-snapshot
Chemical root to shoot signaling under drought
inferredcites →https://doi.org/10.1016/s0176-1617(11)81573-7openalex-snapshot
Electric Signals Released from Roots of Willow (Salix viminalis L.) Change Transpiration and Photosynthesis
inferredcites →https://doi.org/10.1023/a:1004213728734openalex-snapshot
Drought-induced changes in soil contact and hydraulic conductivity for roots of Opuntia ficus-indica with and without rhizosheaths
inferredcites →https://doi.org/10.1038/221281a0openalex-snapshot
Stomatal Closure and Inhibition of Transpiration induced by (RS)-Abscisic Acid
inferredcites →https://doi.org/10.1038/35066500openalex-snapshot
Guard cell abscisic acid signalling and engineering drought hardiness in plants
inferredcites →https://doi.org/10.1038/378715a0openalex-snapshot
Sustained and significant negative water pressure in xylem
inferredcites →https://doi.org/10.1038/srep12449openalex-snapshot
Stomatal closure is induced by hydraulic signals and maintained by ABA in drought-stressed grapevine
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The role of epidermal turgor in stomatal interactions following a local perturbation in humidity
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Vulnerability to cavitation of leaf minor veins: any impact on leaf gas exchange?
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Interactions among stomata in response to perturbations in humidity
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Ultrasound acoustic emissions from dehydrating leaves of deciduous and evergreen trees
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A study of stomatal mechanics using the cell pressure probe
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The guard‐cell apoplast as a site of abscisic acid accumulation in Vicia faba L.
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Ultrasound acoustic emissions from freezing xylem*
inferredcites →https://doi.org/10.1073/pnas.0912021106openalex-snapshot
Activity of guard cell anion channel SLAC1 is controlled by drought-stress signaling kinase-phosphatase pair
inferredcites →https://doi.org/10.1073/pnas.1604088113openalex-snapshot
The correlations and sequence of plant stomatal, hydraulic, and wilting responses to drought
inferredcites →https://doi.org/10.1093/jexbot/53.373.1503openalex-snapshot
Stomatal control in tomato with ABA-deficient roots: response of grafted plants to soil drying
inferredcites →https://doi.org/10.1093/jxb/38.1.126openalex-snapshot
In situObservations of Stomatal Movements
inferredcites →https://doi.org/10.1093/jxb/39.9.1237openalex-snapshot
Acoustic Emissions from Plants: Ultrasonic and Audible Compared
inferredcites →https://doi.org/10.1093/jxb/42.1.123openalex-snapshot
Monitoring of Ultrasonic and Audible Emissions from Plants With or Without Vessels
inferredcites →https://doi.org/10.1093/jxb/42.12.1507openalex-snapshot
Drought-induced Closure ofPhaseolus vulgarisL. Stomata Precedes Leaf Water Deficit and any Increase in Xylem ABA Concentration
inferredcites →https://doi.org/10.1093/jxb/46.1.101openalex-snapshot
The control of leaf conductance of white lupin by xylem ABA concentration decreases with the severity of water deficits
inferredcites →https://doi.org/10.1093/jxb/48.3.665openalex-snapshot
Use of centrifugal force in the study of xylem cavitation
inferredcites →https://doi.org/10.1093/jxb/erj165openalex-snapshot
Rapid hydropassive opening and subsequent active stomatal closure follow heat-induced electrical signals in Mimosa pudica*
inferredcites →https://doi.org/10.1093/jxb/erm338openalex-snapshot
Manipulation of the apoplastic pH of intact plants mimics stomatal and growth responses to water availability and microclimatic variation
inferredcites →https://doi.org/10.1093/jxb/ern171openalex-snapshot
A novel, non-invasive, online-monitoring, versatile and easy plant-based probe for measuring leaf water status
inferredcites →https://doi.org/10.1093/jxb/erw099openalex-snapshot
Long-distance plant signaling pathways in response to multiple stressors: the gap in knowledge
inferredcites →https://doi.org/10.1093/jxb/erx124openalex-snapshot
Up-regulation of NCED3 and ABA biosynthesis occur within minutes of a decrease in leaf turgor but AHK1 is not required
inferredcites →https://doi.org/10.1093/jxb/erx480openalex-snapshot
Leaves, not roots or floral tissue, are the main site of rapid, external pressure-induced ABA biosynthesis in angiosperms
inferredcites →https://doi.org/10.1093/treephys/18.8-9.589openalex-snapshot
A mathematical and statistical analysis of the curves illustrating vulnerability of xylem to cavitation
inferredcites →https://doi.org/10.1093/treephys/19.7.453openalex-snapshot
Regulation of water loss in populations of Populus trichocarpa: the role of stomatal control in preventing xylem cavitation
inferredcites →https://doi.org/10.1093/treephys/25.2.237openalex-snapshot
Field measurements of ultrasonic acoustic emissions and stem diameter variations. New insight into the relationship between xylem tensions and embolism
inferredcites →https://doi.org/10.1093/treephys/tpu056openalex-snapshot
Cavitation: a blessing in disguise? New method to establish vulnerability curves and assess hydraulic capacitance of woody tissues
inferredcites →https://doi.org/10.1093/treephys/tpu080openalex-snapshot
A new type of vulnerability curve: is there truth in vine?
inferredcites →https://doi.org/10.1098/rsif.2014.0480openalex-snapshot
Ultrasonic emissions reveal individual cavitation bubbles in water-stressed wood
inferredcites →https://doi.org/10.1104/pp.102.012856openalex-snapshot
Vulnerability of Xylem Vessels to Cavitation in Sugar Maple. Scaling from Individual Vessels to Whole Branches
inferredcites →https://doi.org/10.1104/pp.103.023879openalex-snapshot
Stomatal Closure during Leaf Dehydration, Correlation with Other Leaf Physiological Traits
inferredcites →https://doi.org/10.1104/pp.106.089250openalex-snapshot
Intact Plant Magnetic Resonance Imaging to Study Dynamics in Long-Distance Sap Flow and Flow-Conducting Surface Area
inferredcites →https://doi.org/10.1104/pp.106.089334openalex-snapshot
Localization of Mechanisms Involved in Hydropassive and Hydroactive Stomatal Responses of Sambucus nigra to Dry Air
inferredcites →https://doi.org/10.1104/pp.111.2.413openalex-snapshot
Drought-Induced Xylem Dysfunction in Petioles, Branches, and Roots of Populus balsamifera L. and Alnus glutinosa (L.) Gaertn
inferredcites →https://doi.org/10.1104/pp.113.1.209openalex-snapshot
The Propagation of Slow Wave Potentials in Pea Epicotyls
inferredcites →https://doi.org/10.1104/pp.114.252940openalex-snapshot
The Evolution of Mechanisms Driving the Stomatal Response to Vapor Pressure Deficit
inferredcites →https://doi.org/10.1104/pp.126.1.27openalex-snapshot
In Vivo Observation of Cavitation and Embolism Repair Using Magnetic Resonance Imaging,
inferredcites →https://doi.org/10.1104/pp.15.00731openalex-snapshot
How Does Leaf Anatomy Influence Water Transport outside the Xylem?
inferredcites →https://doi.org/10.1104/pp.16.01643openalex-snapshot
Outside-Xylem Vulnerability, Not Xylem Embolism, Controls Leaf Hydraulic Decline during Dehydration
inferredcites →https://doi.org/10.1104/pp.47.4.453openalex-snapshot
Evaluation of Water Stress Control with Polyethylene Glycols by Analysis of Guttation
inferredcites →https://doi.org/10.1104/pp.66.5.809openalex-snapshot
Comparative Resistance of the Soil and the Plant to Water Transport
inferredcites →https://doi.org/10.1104/pp.78.1.66openalex-snapshot
In Situ Measurement of Epidermal Cell Turgor, Leaf Water Potential, and Gas Exchange in Tradescantia virginiana L.
inferredcites →https://doi.org/10.1105/tpc.112.096404openalex-snapshot
Fern and Lycophyte Guard Cells Do Not Respond to Endogenous Abscisic Acid
inferredcites →https://doi.org/10.1111/1365-3040.ep11592146openalex-snapshot
Concurrent measurements of stem density, leaf and stem water potential, stomatal conductance and cavitation on a spaling of Thuja occidentalis L.
inferredcites →https://doi.org/10.1111/ele.12851openalex-snapshot
Plant resistance to drought depends on timely stomatal closure
inferredcites →https://doi.org/10.1111/j.1365-3040.1989.tb01918.xopenalex-snapshot
Abscisic acid produced in dehydrating roots may enable the plant to measure the water status of the soil
inferredcites →https://doi.org/10.1111/j.1365-3040.2005.01491.xopenalex-snapshot
Dynamics of stomatal water relations following leaf excision
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01594.xopenalex-snapshot
Declining hydraulic efficiency as transpiring leaves desiccate: two types of response*
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01600.xopenalex-snapshot
Anisohydric but isohydrodynamic: seasonally constant plant water potential gradient explained by a stomatal control mechanism incorporating variable plant hydraulic conductance
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01607.xopenalex-snapshot
Distinct roles of electric and hydraulic signals on the reaction of leaf gas exchange upon re‐irrigation in Zea mays L.
inferredcites →https://doi.org/10.1111/j.1365-3040.2006.01614.xopenalex-snapshot
Electrical signals and their physiological significance in plants
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01831.xopenalex-snapshot
Abscisic acid signalling when soil moisture is heterogeneous: decreased photoperiod sap flow from drying roots limits abscisic acid export to the shoots
inferredcites →https://doi.org/10.1111/j.1365-3040.2010.02127.xopenalex-snapshot
The Impact of Vessel Size on Vulnerability Curves: Data and Models for Within-Species Variability in Saplings of Aspen,Populus tremuloidesMichx
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Vulnerability curves by centrifugation: is there an open vessel artefact, and are ‘r’ shaped curves necessarily invalid?
inferredcites →https://doi.org/10.1111/j.1365-313x.2007.03234.xopenalex-snapshot
A hydraulic signal in root‐to‐shoot signalling of water shortage
inferredcites →https://doi.org/10.1111/j.1399-3054.2012.01605.xopenalex-snapshot
An improved method and data analysis for ultrasound acoustic emissions and xylem vulnerability in conifer wood
inferredcites →https://doi.org/10.1111/j.1438-8677.1928.tb00324.xopenalex-snapshot
32. L. Iwanoff: Zur Methodik der Transpirationsbestimmung am Standort
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Effects of environmental parameters and irrigation on the turgor pressure of banana plants measured using the non‐invasive, online monitoring leaf patch clamp pressure probe
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01460.xopenalex-snapshot
In the light of stomatal opening: new insights into ‘the Watergate’
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Extraction of features from ultrasound acoustic emissions: a tool to assess the hydraulic vulnerability of Norway spruce trunkwood?
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04118.xopenalex-snapshot
No evidence for an open vessel effect in centrifuge‐based vulnerability curves of a long‐vesselled liana (Vitis vinifera)
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Measurements of stem xylem hydraulic conductivity in the laboratory and field
inferredcites →https://doi.org/10.1111/nph.12832openalex-snapshot
Closing gaps: linking elements that control stomatal movement
inferredcites →https://doi.org/10.1111/nph.13017openalex-snapshot
The standard centrifuge method accurately measures vulnerability curves of long‐vesselled olive stems
inferredcites →https://doi.org/10.1111/nph.13476openalex-snapshot
Xylem cavitation resistance can be estimated based on time‐dependent rate of acoustic emissions
inferredcites →https://doi.org/10.1111/pce.12313openalex-snapshot
Relax and refill: xylem rehydration prior to hydraulic measurements favours embolism repair in stems and generates artificially low PLC values
inferredcites →https://doi.org/10.1111/pce.12633openalex-snapshot
Stomatal responses to vapour pressure deficit are regulated by high speed gene expression in angiosperms
inferredcites →https://doi.org/10.1111/pce.12774openalex-snapshot
Most stomatal closure in woody species under moderate drought can be explained by stomatal responses to leaf turgor
inferredcites →https://doi.org/10.1111/pce.12800openalex-snapshot
Osmotic adjustment is a prime drought stress adaptive engine in support of plant production
inferredcites →https://doi.org/10.1111/pce.12852openalex-snapshot
Predicting stomatal responses to the environment from the optimization of photosynthetic gain and hydraulic cost
inferredcites →https://doi.org/10.1111/pce.13335openalex-snapshot
Coordinated plasticity maintains hydraulic safety in sunflower leaves
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Intraspecific variation in embolism resistance and stem anatomy across four sunflower ( Helianthus annuus L.) accessions
inferredcites →https://doi.org/10.1111/tpj.13460openalex-snapshot
Analysis of plant hormone profiles in response to moderate dehydration stress
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-114707openalex-snapshot
Diverse Stomatal Signaling and the Signal Integration Mechanism
inferredcites →https://doi.org/10.1146/annurev.arplant.40.1.19openalex-snapshot
Vulnerability Of Xylem To Cavitation And Embolism
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Stomatal Conductance and Photosynthesis
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The Monitoring of Drying Cracks in the Tension and Opposite Wood by Acoustic Emission and Scanning Electron Microscopy Methods
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Relationship of Carbohydrate and Abscisic Acid Levels to Kernel Set in Maize under Postpollination Water Deficit
inferredcites →https://doi.org/10.2307/2446046openalex-snapshot
Vessel contents during transpiration—embolisms and refilling
inferredcites →https://doi.org/10.2525/ecb.45.59openalex-snapshot
Correlation between Acoustic Emissions Generated from Cavitation in Rubber Tree Leaf Veins
inferredcites →https://doi.org/10.2525/ecb.47.127openalex-snapshot
Estimation for Embolism Risk of Tomato Using Acoustic Emission Response to Increased Drought Stress
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
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Analysis of Constituents for Phenotyping Drought Tolerance in Crop Improvement
inferredcites →https://doi.org/10.3389/fpls.2013.00265openalex-snapshot
Analysis of spatial and temporal dynamics of xylem refilling in Acer rubrum L. using magnetic resonance imaging
inferredcites →https://doi.org/10.3389/fpls.2013.00368openalex-snapshot
Functional analysis of embolism induced by air injection in Acer rubrum and Salix nigra
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
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Highlight Induced Transcriptional Priming against a Subsequent Drought Stress in Arabidopsis thaliana
inferred← citeshttps://doi.org/10.3390/ijms26136008openalex-snapshot
Genome-Wide Identification and Expression Profiling of SlGeBP Gene Family in Response to Hormone and Abiotic Stresses in Solanum lycopersicum L.
inferred← citeshttps://doi.org/10.3390/su15054206openalex-snapshot
Biochar Application Maintains Photosynthesis of Cabbage by Regulating Stomatal Parameters in Salt-Stressed Soil
inferred← citeshttps://doi.org/10.5194/bg-19-4705-2022openalex-snapshot
Technical note: Common ambiguities in plant hydraulics
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120728openalex-snapshot
Additional file 10 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120731openalex-snapshot
Additional file 11 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120734openalex-snapshot
Additional file 12 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120737openalex-snapshot
Additional file 13 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120740openalex-snapshot
Additional file 14 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120743openalex-snapshot
Additional file 15 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120746openalex-snapshot
Additional file 1 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120749openalex-snapshot
Additional file 2 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120752openalex-snapshot
Additional file 3 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120755openalex-snapshot
Additional file 4 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120758openalex-snapshot
Additional file 5 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120761openalex-snapshot
Additional file 6 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120764openalex-snapshot
Additional file 7 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120770openalex-snapshot
Additional file 8 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.6084/m9.figshare.13120773openalex-snapshot
Additional file 9 of Weighted gene coexpression network analysis-based identification of key modules and hub genes associated with drought sensitivity in rice
inferred← citeshttps://doi.org/10.61186/ifej.11.22.22openalex-snapshot
Prediction of Establishment in Progenies of Persian Oak Trees Based on the Morphological and Chlorophyll Fluorescence Traits
inferred← citeshttps://doi.org/10.7831/ras.10.0_168openalex-snapshot
Drought Stress: Responses and Mechanism in Plants
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