On the public citation graph
Rapid alterations in growth rate and electrical potentials upon stem excision in pea seedlings
0 signed · 116 inferred · view as graph
Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.
Is this your work? Sign in with ORCID and put your name on the
claims that are yours.
Reference health. See whether every reference in this work resolves to a
known work and none has been retracted — and get a dated CiteStamped
badge you can embed.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-3-642-68752-5_3openalex-snapshot
Cell Electrophysiology and Membrane Transport
inferredcites →https://doi.org/10.1007/bf00195341openalex-snapshot
Measurement of negative pressure in the xylem of excised roots
inferredcites →https://doi.org/10.1007/bf00201510openalex-snapshot
Stretch-activated chloride, potassium, and calcium channels coexisting in plasma membranes of guard cells of Vicia faba L.
inferredcites →https://doi.org/10.1007/bf00386758openalex-snapshot
Action potentials resulting from mechanical stimulation of pea epicotyls
inferredcites →https://doi.org/10.1007/bf00386892openalex-snapshot
Electrical coupling between cells of higher plants: A direct demonstration of intercellular communication
inferredcites →https://doi.org/10.1007/bf00390327openalex-snapshot
Phytochrome control of electrical potentials and intercellular coupling in oat-coleoptile tissue
inferredcites →https://doi.org/10.1007/bf00391104openalex-snapshot
Wall relaxation in growing stems: comparison of four species and assessment of measurement techniques
inferredcites →https://doi.org/10.1007/bf00392486openalex-snapshot
Mechanism of rapid suppression of cell expansion in cucumber hypocotyls after blue-light irradiation
inferredcites →https://doi.org/10.1007/bf00397898openalex-snapshot
Electrical characteristics of stomatal guard cells: The ionic basis of the membrane potential and the consequence of potassium chlorides leakage from microelectrodes
inferredcites →https://doi.org/10.1007/bf01868950openalex-snapshot
“Metabolic” action potentials inAcetabularia
inferredcites →https://doi.org/10.1007/bf01870620openalex-snapshot
Current-voltage relationships of potassium channels in the plasmalemma ofAcetabularia
inferredcites →https://doi.org/10.1007/bf01911266openalex-snapshot
Über die Erregungssubstanz der Mimosoideen
inferredcites →https://doi.org/10.1016/0005-2736(81)90282-0openalex-snapshot
A study of the current-voltage relationships of electrogenetic active and passive membrane elements in riccia fluitans
inferredcites →https://doi.org/10.1016/0014-5793(77)80221-4openalex-snapshot
Light‐induced reversible proton extrusion by spinach‐chloroplast photosystem II vesicles isolated by phase partition
inferredcites →https://doi.org/10.1016/0014-5793(88)80188-1openalex-snapshot
A stretch‐activated anion channel in tobacco protoplasts
inferredcites →https://doi.org/10.1016/0160-9327(84)90003-6openalex-snapshot
Turgorins—new chemical messengers for plant behaviour
inferredcites →https://doi.org/10.1016/0304-4211(82)90013-xopenalex-snapshot
Control of proton efflux from corn root tissue by an injury-sensing mechanism
inferredcites →https://doi.org/10.1016/0304-4211(82)90160-2openalex-snapshot
Rapid inhibition of hypocotyl growth by blue light in Sinapis alba L.
inferredcites →https://doi.org/10.1016/s0015-3796(89)80056-3openalex-snapshot
Investigation of the Wave of Electric Depolarization Induced by Wounding in Bidens pilosus L.: Effects of Weak Acids on the Transmembrane Potential and on the Elicitation of the Wave
inferredcites →https://doi.org/10.1073/pnas.78.4.2422openalex-snapshot
Intercellular communication in plants: Evidence for a rapidly generated, bidirectionally transmitted wound signal
inferredcites →https://doi.org/10.1093/jxb/26.1.131openalex-snapshot
Cell Membrane Potentials of Higher Plants: Changes Induced by Wounding
inferredcites →https://doi.org/10.1093/jxb/29.5.1205openalex-snapshot
Plasmolysis, Plasmodesmata, and the Electrical Coupling of Oat Coleoptile Cells
inferredcites →https://doi.org/10.1093/jxb/35.2.204openalex-snapshot
Effect of Excision on Leaf Water Potential
inferredcites →https://doi.org/10.1093/jxb/42.1.131openalex-snapshot
Characteristics of the Wave of Depolarization Induced by Wounding inBidens pilosaL.
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a076182openalex-snapshot
Electrotonic Coupling between Adjacent Internodal Cells of Chara braunii: Transmission of Action Potentials beyond the Node
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077027openalex-snapshot
Propagation in Vicia faba Stem of a Potential Variation Induced by Wounding
inferredcites →https://doi.org/10.1093/oxfordjournals.pcp.a077843openalex-snapshot
A Pressure-Jump Method as a New Tool in Growth Physiology for Monitoring Physiological Wall Extensibility and Effective Turgor
inferredcites →https://doi.org/10.1104/pp.45.4.415openalex-snapshot
Stomatal Responses to Pressure Changes and Interruptions in the Water Supply of Detached Leaves of Zea mays L.
inferredcites →https://doi.org/10.1104/pp.48.5.631openalex-snapshot
Immediate and Subsequent Growth Responses of Maize Leaves to Changes in Water Status
inferredcites →https://doi.org/10.1104/pp.57.2.123openalex-snapshot
Transmembrane Electropotential in Barley Roots as Related to Cell Type, Cell Location, and Cutting and Aging Effects
inferredcites →https://doi.org/10.1104/pp.58.5.636openalex-snapshot
Turgor Pressure Sensing in Plant Cell Membranes
inferredcites →https://doi.org/10.1104/pp.59.3.369openalex-snapshot
Osmotic Shock Inhibits Auxin-stimulated Acidification and Growth
inferredcites →https://doi.org/10.1104/pp.62.3.423openalex-snapshot
Growth-induced Water Potentials in Plant Cells and Tissues
inferredcites →https://doi.org/10.1104/pp.67.4.864openalex-snapshot
Electrochemical Aging Responses in Pisum: Cellular Adaptations or Recovery from Injury?
inferredcites →https://doi.org/10.1104/pp.82.4.1148openalex-snapshot
Electrical Evidence for Turgor Inhibition of Proton Extrusion in Sugar Beet Taproot
inferredcites →https://doi.org/10.1104/pp.89.1.184openalex-snapshot
Mechanism of Gibberellin-Dependent Stem Elongation in Peas
inferredcites →https://doi.org/10.1104/pp.93.4.1601openalex-snapshot
Primary Events Regulating Stem Growth at Low Water Potentials
inferredcites →https://doi.org/10.1104/pp.94.4.1625openalex-snapshot
Coupling of Solute Transport and Cell Expansion in Pea Stems
inferredcites →https://doi.org/10.1111/j.1365-3040.1987.tb01844.xopenalex-snapshot
Action potentials as multifunctional signals in plants: a unifying hypothesis to explain apparently disparate wound responses
inferredcites →https://doi.org/10.1111/j.1365-3040.1991.tb00953.xopenalex-snapshot
Surface potentials and hydraulic signals in wheat leaves following localized wounding by heat
inferredcites →https://doi.org/10.1111/j.1399-3054.1966.tb07039.xopenalex-snapshot
Quantitative Determinations of the Effect of Excision on Transpiration
inferredcites →https://doi.org/10.1111/j.1438-8677.1988.tb00052.xopenalex-snapshot
Transmission of Electric Signals in Sieve Tubes of Zucchini Plants
inferredcites →https://doi.org/10.1126/science.143.3613.1448openalex-snapshot
Electrical Resistance of Cell Membranes of Avena coleoptiles
inferredcites →https://doi.org/10.1139/b76-285openalex-snapshot
Mediation of rapid electrical, metabolic, transpirational, and photosynthetic changes by factors released from wounds. II. Mediation of the variation potential by Ricca's factor
inferredcites →https://doi.org/10.1139/b84-064openalex-snapshot
The effect of humidity, root excision, and potassium supply on hypocotyl elongation in dark-grown seedlings of Helianthus annuus
inferredcites →https://doi.org/10.1242/jcs.2.3.451openalex-snapshot
Plasmodesmata in Nitella translucens: Structure and electrical resistance
inferredcites →https://doi.org/10.15281/jplantres1887.68.337openalex-snapshot
Electrical Change Caused by Blazing in a Non-sensitive Plant
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/9781118382806.ch6openalex-snapshot
Cellular Basis of Electrical Potential Waves along the Phloem and Impact of Coincident Ca2+Fluxes
inferred← citeshttps://doi.org/10.1007/3-540-28516-4_20openalex-snapshot
Slow Wave Potentials – a Propagating Electrical Signal Unique to Higher Plants
inferred← citeshttps://doi.org/10.1007/978-1-4939-9562-2_34openalex-snapshot
Measurement of Electropotential Waves in Intact Phloem Sieve Elements Using Microelectrodes
inferred← citeshttps://doi.org/10.1007/978-3-319-24049-7_1openalex-snapshot
Plant-Herbivore Interactions in the Era of Big Data
inferred← citeshttps://doi.org/10.1007/978-3-642-36470-9_15openalex-snapshot
Electrical Long-Distance Signaling in Plants
inferred← citeshttps://doi.org/10.1007/978-3-642-36470-9_18openalex-snapshot
Calcium as a Trigger and Regulator of Systemic Alarms and Signals along the Phloem Pathway
inferred← citeshttps://doi.org/10.1007/bf00231397openalex-snapshot
Induction and ionic basis of slow wave potentials in seedlings of Pisum sativum L.
inferred← citeshttps://doi.org/10.1007/s00232-013-9529-8openalex-snapshot
Simulation of Variation Potential in Higher Plant Cells
inferred← citeshttps://doi.org/10.1007/s00425-004-1363-xopenalex-snapshot
Decrement and amplification of slow wave potentials during their propagation in Helianthus annuus L. shoots
inferred← citeshttps://doi.org/10.1007/s004250000514openalex-snapshot
Long-distance signaling within Coleus × hybridus leaves; mediated by changes in intra-leaf CO 2 ?
inferred← citeshttps://doi.org/10.1007/s11103-010-9599-2openalex-snapshot
Axillary bud outgrowth in herbaceous shoots: how do strigolactones fit into the picture?
inferred← citeshttps://doi.org/10.1007/s11738-000-0010-9openalex-snapshot
The effects of freezing on membrane electric potential in winter oilseed rape leaves
inferred← citeshttps://doi.org/10.1016/j.bpc.2024.107199openalex-snapshot
Dependence of cell's membrane potential on extracellular voltage observed in Chara globularis
inferred← citeshttps://doi.org/10.1016/j.cjac.2022.100211openalex-snapshot
The monitoring of plant physiology and ecology: From materials to flexible devices
inferred← citeshttps://doi.org/10.1016/j.jplph.2012.02.013openalex-snapshot
The mechanism of propagation of variation potentials in wheat leaves
inferred← citeshttps://doi.org/10.1016/j.pbi.2017.12.009openalex-snapshot
Systemic signaling in response to wounding and pathogens
inferred← citeshttps://doi.org/10.1016/j.pbiomolbio.2018.11.009openalex-snapshot
Long-distance electrical signals as a link between the local action of stressors and the systemic physiological responses in higher plants
inferred← citeshttps://doi.org/10.1016/s0168-9452(96)04567-0openalex-snapshot
The effect of wounding the roots by high temperature on the respiration rate of the shoot and propagation of electric signal in horse bean seedlings (Vicia faba L. minor)
inferred← citeshttps://doi.org/10.1023/a:1010718020095openalex-snapshot
Long-distance signalling and a mutational analysis of branching in pea
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1997.1010219.xopenalex-snapshot
Slow wave potentials in cucumber differ in form and growth effect from those in pea seedlings
inferred← citeshttps://doi.org/10.1038/nprot.2014.136openalex-snapshot
Measuring surface potential changes on leaves
inferred← citeshttps://doi.org/10.1046/j.1365-3040.1997.d01-141.xopenalex-snapshot
Mannitol inhibits growth of intact cucumber but not pea seedlings by mechanically collapsing the root pressure
inferred← citeshttps://doi.org/10.1046/j.1365-3040.1997.d01-7.xopenalex-snapshot
A reduced xylem pressure altered the electric and growth responses in cucumber hypocotyls
inferred← citeshttps://doi.org/10.1046/j.1365-313x.2002.01426.xopenalex-snapshot
On‐line measurements of K+ activity in the tensile water of the xylem conduit of higher plants
inferred← citeshttps://doi.org/10.1071/pp96036openalex-snapshot
Cortical Intracellular Electrical Potential in Roots of Unstressed and Stressed Sunflower Seedlings. I. Dependence on Water Status
inferred← citeshttps://doi.org/10.1071/pp98098openalex-snapshot
Hydraulic and electrical transmission of wound-induced signals in Vitis vinifera
inferred← citeshttps://doi.org/10.1073/pnas.1907379116openalex-snapshot
Arabidopsis H + -ATPase AHA1 controls slow wave potential duration and wound-response jasmonate pathway activation
inferred← citeshttps://doi.org/10.1073/pnas.2422692122openalex-snapshot
A unified framework for hydromechanical signaling can explain transmission of local and long-distance signals in plants
inferred← citeshttps://doi.org/10.1080/15592324.2015.1057365openalex-snapshot
Variation potential in higher plants: Mechanisms of generation and propagation
inferred← citeshttps://doi.org/10.1080/15592324.2018.1486145openalex-snapshot
Microwave radiation alters burn injury-evoked electric potential in Nicotiana benthamiana
inferred← citeshttps://doi.org/10.1080/15592324.2025.2567930openalex-snapshot
Characterization of wound-induced electrical signals and reactive oxygen species in chickpea (Cicer arietinum)
inferred← citeshttps://doi.org/10.1093/jxb/44.4.741openalex-snapshot
Wound-Induced Hydraulic Signals: Survey of Occurrence in a Range of Species
inferred← citeshttps://doi.org/10.1093/jxb/erac449openalex-snapshot
Osmoelectric siphon models for signal and water dispersal in wounded plants
inferred← citeshttps://doi.org/10.1093/jxb/ert425openalex-snapshot
Spread the news: systemic dissemination and local impact of Ca2+ signals along the phloem pathway
inferred← citeshttps://doi.org/10.1093/oxfordjournals.pcp.a029367openalex-snapshot
The Wound Response in Tomato Involves Rapid Growth and Electrical Responses, Systemically Up-Regulated Transcription of Proteinase Inhibitor and Calmodulin and Down-Regulated Translation
inferred← citeshttps://doi.org/10.1093/pcp/pcu082openalex-snapshot
Ionic Nature of Burn-Induced Variation Potential in Wheat Leaves
inferred← citeshttps://doi.org/10.1101/2024.10.23.619842openalex-snapshot
A unified framework for hydromechanical signaling: Do plant signals go with the flow?
inferred← citeshttps://doi.org/10.1104/pp.104.058743openalex-snapshot
Auxin Dynamics after Decapitation Are Not Correlated with the Initial Growth of Axillary Buds
inferred← citeshttps://doi.org/10.1104/pp.104.4.1385openalex-snapshot
Hydraulic Signals from the Roots and Rapid Cell-Wall Hardening in Growing Maize (Zea mays L.) Leaves Are Primary Responses to Polyethylene Glycol-Induced Water Deficits
inferred← citeshttps://doi.org/10.1104/pp.109.135475openalex-snapshot
Roles for Auxin, Cytokinin, and Strigolactone in Regulating Shoot Branching
inferred← citeshttps://doi.org/10.1104/pp.113.1.209openalex-snapshot
The Propagation of Slow Wave Potentials in Pea Epicotyls
inferred← citeshttps://doi.org/10.1104/pp.115.3.1083openalex-snapshot
Characterization of the Variation Potential in Sunflower
inferred← citeshttps://doi.org/10.1104/pp.123.2.689openalex-snapshot
Auxin Inhibition of Decapitation-Induced Branching Is Dependent on Graft-Transmissible Signals Regulated by GenesRms1andRms2
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1993.tb00904.xopenalex-snapshot
Isoprene emission by plants is affected by transmissible wound signals
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1994.tb02012.xopenalex-snapshot
Comparison of electric and growth responses to excision in cucumber and pea seedlings. I. Short‐distance effects are a result of wounding
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1995.tb00541.xopenalex-snapshot
Comparison of electric and growth responses to excision in cucumber and pea seedlings. II. Long‐distance effects are caused by the release of xylem pressure
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2006.01614.xopenalex-snapshot
Electrical signals and their physiological significance in plants
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2008.01922.xopenalex-snapshot
Heat‐induced electrical signals affect cytoplasmic and apoplastic pH as well as photosynthesis during propagation through the maize leaf
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2012.02571.xopenalex-snapshot
Interaction of xylem and phloem during exudation and wound occlusion in Cucurbita maxima
inferred← citeshttps://doi.org/10.1111/nph.12897openalex-snapshot
The squeeze cell hypothesis for the activation of jasmonate synthesis in response to wounding
inferred← citeshttps://doi.org/10.1111/nph.16646openalex-snapshot
Wound‐ and mechanostimulated electrical signals control hormone responses
inferred← citeshttps://doi.org/10.1111/pce.12150openalex-snapshot
Involvement of respiratory processes in the transient knockout of net CO2 uptake in M imosa pudica upon heat stimulation
inferred← citeshttps://doi.org/10.1111/ppl.12208openalex-snapshot
Influence of variation potential on resistance of the photosynthetic machinery to heating in pea
inferred← citeshttps://doi.org/10.1126/scisignal.aba1453openalex-snapshot
Two glutamate- and pH-regulated Ca 2+ channels are required for systemic wound signaling in Arabidopsis
inferred← citeshttps://doi.org/10.1134/s0006350908010144openalex-snapshot
What are the genuine action potentials in plants?
inferred← citeshttps://doi.org/10.1134/s0006350916030209openalex-snapshot
Electrical signals in higher plants: Mechanisms of generation and propagation
inferred← citeshttps://doi.org/10.1371/journal.pone.0286103openalex-snapshot
Summation of activation at the branch-stem transition of Mimosa pudica; a comparison with summation in cardiac tissue
inferred← citeshttps://doi.org/10.20944/preprints202111.0129.v1openalex-snapshot
Root-To-Shoot Signaling for the Coding of Support Thickness in Pea Plants
inferred← citeshttps://doi.org/10.3389/fpls.2013.00239openalex-snapshot
Electrical signaling along the phloem and its physiological responses in the maize leaf
inferred← citeshttps://doi.org/10.3389/fpls.2019.01393openalex-snapshot
Shear-Enhanced Dispersion of a Wound Substance as a Candidate Mechanism for Variation Potential Transmission
inferred← citeshttps://doi.org/10.3389/fpls.2020.610445openalex-snapshot
Breaking Bad News: Dynamic Molecular Mechanisms of Wound Response in Plants
inferred← citeshttps://doi.org/10.3390/ijms221910715openalex-snapshot
Electrical Signaling of Plants under Abiotic Stressors: Transmission of Stimulus-Specific Information
inferred← citeshttps://doi.org/10.3390/plants13202896openalex-snapshot
Analysis of the Mechanisms Underlying the Specificity of the Variation Potential Induced by Different Stimuli
inferred← citeshttps://doi.org/10.3390/plants9101364openalex-snapshot
Spatial and Temporal Dynamics of Electrical and Photosynthetic Activity and the Content of Phytohormones Induced by Local Stimulation of Pea Plants
inferred← citeshttps://doi.org/10.4161/psb.1.1.2275openalex-snapshot
Shade-Induced Action Potentials inHelianthus annuusL. Originate Primarily from the Epicotyl
inferred← citeshttps://doi.org/10.4161/psb.4.2.7872openalex-snapshot
Electrical signaling, stomatal conductance, ABA and Ethylene content in avocado trees in response to root hypoxia
Editorial review for independent work. ICSAC — the Institute for Complexity
Science and Advanced Computing — runs a structured editorial panel for researchers
publishing outside journals, and publishes on CiteStamp rails. Submission is free
and goes through ORCID: icsacinstitute.org/submit.