On the public citation graph
Hydraulic Resistance of Plants. III. Effects of NaCl in Barley and Lupin
0 signed · 141 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known work and none has been retracted — and get a dated CiteStamped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/10.1071/bi9670723openalex-snapshot
Effects of Osmotic Pressure on Exudation from Corn Roots
inferredcites →https://doi.org/10.1071/pp9780469openalex-snapshot
Osmotically Induced Changes in the Pressure-Flow Relationship of Maize Root Systems
inferredcites →https://doi.org/10.1071/pp9840333openalex-snapshot
Hydraulic Resistance of Plants. I. Constant or Variable?
inferredcites →https://doi.org/10.1071/pp9840341openalex-snapshot
Hydraulic Resistance of Plants. II. Effects of Rooting Medium, and Time of Day, in Barley and Lupin
inferredcites →https://doi.org/10.1071/sr9670149openalex-snapshot
Numerical analysis of the convection and diffusion of solutes to roots
inferredcites →https://doi.org/10.1093/jxb/31.1.333openalex-snapshot
The Transport of Water from Soil to Shoot in Wheat Seedlings
inferredcites →https://doi.org/10.1104/pp.71.4.810openalex-snapshot
An Interpretation of Some Whole Plant Water Transport Phenomena
inferredcites →https://doi.org/10.1111/j.1399-3054.1976.tb03995.xopenalex-snapshot
Salinity and the Hydraulic Conductance of Roots
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1016/j.phytochem.2021.112774zenodo-depositor-declared
The complexity of sound quantification of specialized metabolite biosynthesis: The stress related impact on the alkaloid content of Catharanthus roseus
inferred← citeshttps://doi.org/10.1002/jpln.200900222openalex-snapshot
Responses of Batis maritima plants challenged with up to two‐fold seawater NaCl salinity
inferred← citeshttps://doi.org/10.1006/anbo.1998.0781openalex-snapshot
Water Retention Capacity in Root Segments Differing in the Degree of Exodermis Development
inferred← citeshttps://doi.org/10.1006/jtbi.2000.2194openalex-snapshot
Some Compartmental Models of the Root: Steady-state Behavior
inferred← citeshttps://doi.org/10.1007/978-1-4614-4747-4_6openalex-snapshot
Adaptive Plasticity of Salt-Stressed Root Systems
inferred← citeshttps://doi.org/10.1007/978-3-030-04417-6_20openalex-snapshot
Different Antioxidant Defense Systems in Halophytes and Glycophytes to Overcome Salinity Stress
inferred← citeshttps://doi.org/10.1007/978-3-030-63497-1_3openalex-snapshot
Genotypic Selection in Vegetables for Adaptation to Climate Change
inferred← citeshttps://doi.org/10.1007/978-3-032-01704-8_2openalex-snapshot
Functional Genomics Approaches for Abiotic Stress Tolerance Mechanism in Crop Plants
inferred← citeshttps://doi.org/10.1007/978-3-322-91216-9_8openalex-snapshot
Einfluß der Bodenart auf die Ausbildung osmotischer Potentialgradienten zwischen Gesamtboden und Rhizosphäre
inferred← citeshttps://doi.org/10.1007/978-3-642-19106-0_10openalex-snapshot
Hydraulic Architecture of Vascular Plants
inferred← citeshttps://doi.org/10.1007/978-94-009-4356-8_10openalex-snapshot
Translocation and metabolism of nitrogen: whole plant aspects
inferred← citeshttps://doi.org/10.1007/978-94-009-4816-7_1openalex-snapshot
References no. 12912-14765/ABD-ZUR
inferred← citeshttps://doi.org/10.1007/978-94-011-1858-3_30openalex-snapshot
Importance of mineral nutrient cycling for salinity tolerance of plants
inferred← citeshttps://doi.org/10.1007/978-94-017-3101-0_26openalex-snapshot
Water transport across roots
inferred← citeshttps://doi.org/10.1007/bf00010347openalex-snapshot
Soil solute concentration and water uptake by single lupin and radish plant roots
inferred← citeshttps://doi.org/10.1007/bf00010348openalex-snapshot
Soil solute concentration and water uptake by single lupin and radish plant roots
inferred← citeshttps://doi.org/10.1007/bf00010541openalex-snapshot
Growth and ion accumulation of two rapid-cycling Brassica species differing in salt tolerance
inferred← citeshttps://doi.org/10.1007/bf00020863openalex-snapshot
Collection and composition of xylem sap and root structure in two halophytic species
inferred← citeshttps://doi.org/10.1007/bf00401022openalex-snapshot
Growth response of barley and tomato to nitrogen stress and its control by abscisic acid, water relations and photosynthesis
inferred← citeshttps://doi.org/10.1007/s00299-023-03067-wopenalex-snapshot
Transcriptome profiling reveals multiple regulatory pathways of Tamarix chinensis in response to salt stress
inferred← citeshttps://doi.org/10.1007/s11104-004-8070-zopenalex-snapshot
Roles of Aquaporins in Root Responses to Irrigation
inferred← citeshttps://doi.org/10.1007/s11104-005-7010-xopenalex-snapshot
Are Root Hydraulic Conductivity Responses to Salinity Controlled by Aquaporins in Broccoli Plants?
inferred← citeshttps://doi.org/10.1007/s11104-013-1736-7openalex-snapshot
Uptake of water from a Kandosol subsoil. II. Control of water uptake by roots
inferred← citeshttps://doi.org/10.1007/s11104-019-04408-zopenalex-snapshot
Linear relation between leaf xylem water potential and transpiration in pearl millet during soil drying
inferred← citeshttps://doi.org/10.1007/s11738-010-0677-5openalex-snapshot
Osmotic adjustment, water relations and growth attributes of the xero-halophyte Reaumuria vermiculata L. (Tamaricaceae) in response to salt stress
inferred← citeshttps://doi.org/10.1007/s12042-025-09411-6openalex-snapshot
Genome Wide Identification, Expression Profiles and Regulatory Network Analysis of SOS Group of Genes in Camellia Sinensis
inferred← citeshttps://doi.org/10.1016/b978-0-12-633070-0.50013-xopenalex-snapshot
The Regulation of Plant Water at the Cell, Tissue, and Organ Level: Role of Active Processes and of Compartmentation
inferred← citeshttps://doi.org/10.1016/b978-0-12-815355-0.00017-5openalex-snapshot
QTL mapping for abiotic stress in legumes
inferred← citeshttps://doi.org/10.1016/b978-0-12-816091-6.00009-2openalex-snapshot
Breeding climate-resilience crops for future agriculture
inferred← citeshttps://doi.org/10.1016/bs.abr.2022.02.015openalex-snapshot
Salinity and night-time transpiration under current climate scenarios
inferred← citeshttps://doi.org/10.1016/j.compag.2016.03.006openalex-snapshot
Electrical impedance spectroscopy: A tool to investigate the responses of one halophyte to different growth and stress conditions
inferred← citeshttps://doi.org/10.1016/j.copbio.2013.12.004openalex-snapshot
Salt resistant crop plants
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2004.01.012openalex-snapshot
Osmotic adjustment, water relations and gas exchange in pepper plants grown under NaCl or KCl
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2006.04.004openalex-snapshot
Computed tomographic evaluation of osmotica on shrinkage and recovery of lupin (Lupinus angustifolius L.) and radish (Raphanus sativus L.) roots
inferred← citeshttps://doi.org/10.1016/j.jplph.2005.07.015openalex-snapshot
Effects of NaCl on the growth, ion accumulation and photosynthetic parameters of Thellungiella halophila
inferred← citeshttps://doi.org/10.1016/j.jplph.2006.07.013openalex-snapshot
Efficiency of biochemical protection against toxic effects of accumulated salt differentiates Thellungiella halophila from Arabidopsis thaliana
inferred← citeshttps://doi.org/10.1016/j.napere.2022.100006openalex-snapshot
A critical review on adaptations, and biological activities of the mangroves
inferred← citeshttps://doi.org/10.1016/j.plantsci.2003.10.010openalex-snapshot
Does calcium determine water uptake under saline conditions in pepper plants, or is it water flux which determines calcium uptake?
inferred← citeshttps://doi.org/10.1016/j.plantsci.2004.10.015openalex-snapshot
K+ starvation increases water uptake in whole sunflower plants
inferred← citeshttps://doi.org/10.1016/j.plaphy.2017.02.001openalex-snapshot
Changes in root hydraulic conductivity facilitate the overall hydraulic response of rice (Oryza sativa L.) cultivars to salt and osmotic stress
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.108168openalex-snapshot
Survival mechanisms of chickpea (Cicer arietinum) under saline conditions
inferred← citeshttps://doi.org/10.1016/j.scienta.2009.09.002openalex-snapshot
Comparison of the responses to NaCl stress of two pea cultivars using split-root system
inferred← citeshttps://doi.org/10.1016/s0065-2113(07)96002-2openalex-snapshot
Water Flow in the Roots of Crop Species: The Influence of Root Structure, Aquaporin Activity, and Waterlogging
inferred← citeshttps://doi.org/10.1016/s0065-2113(08)60242-4openalex-snapshot
Responses of Cool Season Grain Legumes to Soil Abiotic Stresses
inferred← citeshttps://doi.org/10.1016/s0065-2113(08)60464-2openalex-snapshot
Crop Water Deficits: A Decade of Progress
inferred← citeshttps://doi.org/10.1016/s0168-9452(00)00272-7openalex-snapshot
Ammonium, bicarbonate and calcium effects on tomato plants grown under saline conditions
inferred← citeshttps://doi.org/10.1016/s0176-1617(00)80238-2openalex-snapshot
Salinity Resistance of Citrus Seedlings in Relation to Hydraulic Conductance, Plasma Membrane ATPase and Anatomy of the Roots
inferred← citeshttps://doi.org/10.1016/s0176-1617(86)80039-6openalex-snapshot
Effects of NaCl Salinity on Growth, Development, Ion Transport and Ion Storage in White Lupin (Lupinus albus L. cv. Ultra)
inferred← citeshttps://doi.org/10.1023/a:1024527401033openalex-snapshot
Differential effects of salinity on leaf elongation kinetics of three grass species
inferred← citeshttps://doi.org/10.1023/b:plso.0000037034.47247.67openalex-snapshot
Salinity effects on germination, growth, and seed production of the halophyte Cakile maritima
inferred← citeshttps://doi.org/10.1034/j.1399-3054.1999.105115.xopenalex-snapshot
Physiological function of water channels as affected by salinity in roots of paprika pepper
inferred← citeshttps://doi.org/10.1034/j.1399-3054.2002.1150311.xopenalex-snapshot
Water entry into detached root systems saturates with increasing externally applied pressure; a result inconsistent with models of simple passive diffusion
inferred← citeshttps://doi.org/10.1038/s41598-017-01211-7openalex-snapshot
Exploring genetic variation for salinity tolerance in chickpea using image-based phenotyping
inferred← citeshttps://doi.org/10.1046/j.1365-3040.1997.d01-65.xopenalex-snapshot
Xylem and cell turgor pressure probe measurements in intact roots of glycophytes: transpiration induces a change in the radial and cellular reflection coefficients
inferred← citeshttps://doi.org/10.1046/j.1469-8137.1999.00461.xopenalex-snapshot
Simultaneous collection of xylem sap from Rhinanthus minor and the hosts Hordeum and Trifolium: hydraulic properties, xylem sap composition and effects of attachment
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2000.00593.xopenalex-snapshot
Does calcium ameliorate the negative effect of NaCl on melon root water transport by regulating aquaporin activity?
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2000.00625.xopenalex-snapshot
Effects of salinity on xylem structure and water use in growing leaves of sorghum
inferred← citeshttps://doi.org/10.1055/s-2006-924172openalex-snapshot
Plant Aquaporins: New Perspectives on Water and Nutrient Uptake in Saline Environment
inferred← citeshttps://doi.org/10.1071/ar99071openalex-snapshot
Role of soil pH, Ca supply, and banded P fertilisers in modulating ammonia toxicity to wheat
inferred← citeshttps://doi.org/10.1071/fp02035openalex-snapshot
The riddle of root pressure. I. Putting Maxwell's demon to rest
inferred← citeshttps://doi.org/10.1071/fp15284openalex-snapshot
Salt tolerance of the halophyte Limonium delicatulum is more associated with antioxidant enzyme activities than phenolic compounds
inferred← citeshttps://doi.org/10.1071/pp9840333openalex-snapshot
Hydraulic Resistance of Plants. I. Constant or Variable?
inferred← citeshttps://doi.org/10.1071/pp9840497openalex-snapshot
Effect of Prolonged Exposure to Nacl on the Osmotic Pressure of Leaf Xylem Sap From Intact, Transpiring Barley Plants
inferred← citeshttps://doi.org/10.1071/pp99193openalex-snapshot
Leaf water status controls day-time but not daily rates of leaf expansion in salt-treated barley.
inferred← citeshttps://doi.org/10.1071/pp99203openalex-snapshot
Regulation of water channel activity in whole roots and in protoplasts from roots of melon plants grown under saline conditions
inferred← citeshttps://doi.org/10.1073/pnas.161279898openalex-snapshot
Transpiration, a prerequisite for long-distance transport of minerals in plants?
inferred← citeshttps://doi.org/10.1078/0176-1617-00652openalex-snapshot
Water and nutrient uptake of grafted tomato plants grown under saline conditions
inferred← citeshttps://doi.org/10.1078/0176-1617-00861openalex-snapshot
Influence of saline stress on root hydraulic conductance and PIP expression inArabidopsis
inferred← citeshttps://doi.org/10.1080/00103629709369792openalex-snapshot
The effect of gypsum and other salts on the growth of narrow‐leafed lupins
inferred← citeshttps://doi.org/10.1080/0021213x.1990.10677149openalex-snapshot
INTERACTIVE EFFECTS OF SALINITY AND CALCIUM ON HYDRAULIC CONDUCTIVITY, OSMOTIC ADJUSTMENT, AND GROWTH IN PRIMARY ROOTS OF MAIZE SEEDLINGS
inferred← citeshttps://doi.org/10.1080/01904169209364363openalex-snapshot
Effects of salinity stress and calcium on hydraulic conductivity and growth in maize seedling roots
inferred← citeshttps://doi.org/10.1080/11263504.2010.514130openalex-snapshot
Influence of salinity on root hydraulic properties of three olive varieties
inferred← citeshttps://doi.org/10.1080/17429145.2020.1722267openalex-snapshot
OsRuvB transgene induces salt tolerance in pigeon pea
inferred← citeshttps://doi.org/10.1081/pln-120018567openalex-snapshot
Responses of Radial and Axial Hydraulic Resistances in Maize Root to Nitrogen Availability
inferred← citeshttps://doi.org/10.1086/520722openalex-snapshot
The Phi Thickening in Roots of Broccoli Plants: An Acclimation Mechanism to Salinity?
inferred← citeshttps://doi.org/10.1093/aob/mcw191openalex-snapshot
Evaluating physiological responses of plants to salinity stress
inferred← citeshttps://doi.org/10.1093/jexbot/49.322.879openalex-snapshot
Rapid acclimation of root hydraulic conductivity to low temperature
inferred← citeshttps://doi.org/10.1093/jexbot/51.350.1531openalex-snapshot
Water uptake by roots: effects of water deficit
inferred← citeshttps://doi.org/10.1093/jxb/42.11.1417openalex-snapshot
Kinetics of Maize Leaf Elongation
inferred← citeshttps://doi.org/10.1093/jxb/42.2.143openalex-snapshot
Root Hydraulic Conductivity of Two Cactus Species in Relation to Root Age, Temperature, and Soil Water Status
inferred← citeshttps://doi.org/10.1093/jxb/42.9.1105openalex-snapshot
Cation and Chloride Partitioning through Xylem and Phloem within the Whole Plant ofRicinus communisL. under Conditions of Salt Stress
inferred← citeshttps://doi.org/10.1093/jxb/erq312openalex-snapshot
Water uptake by seminal and adventitious roots in relation to whole-plant water flow in barley (Hordeum vulgare L.)
inferred← citeshttps://doi.org/10.1093/jxb/ery183openalex-snapshot
Hydraulic processes in roots and the rhizosphere pertinent to increasing yield of water-limited grain crops: a critical review
inferred← citeshttps://doi.org/10.1093/pcp/pcr027openalex-snapshot
Mechanisms of Water Transport Mediated by PIP Aquaporins and Their Regulation Via Phosphorylation Events Under Salinity Stress in Barley Roots
inferred← citeshttps://doi.org/10.1093/plphys/kiab271openalex-snapshot
Soil textures rather than root hairs dominate water uptake and soil–plant hydraulics under drought
inferred← citeshttps://doi.org/10.1104/pp.105.065029openalex-snapshot
Early Effects of Salinity on Water Transport in Arabidopsis Roots. Molecular and Cellular Features of Aquaporin Expression
inferred← citeshttps://doi.org/10.1104/pp.110.163113openalex-snapshot
Natural Variation of Root Hydraulics in Arabidopsis Grown in Normal and Salt-Stressed Conditions
inferred← citeshttps://doi.org/10.1104/pp.124.2.767openalex-snapshot
Effects of Elevated [CO2] and Nitrogen Nutrition on Cytokinins in the Xylem Sap and Leaves of Cotton
inferred← citeshttps://doi.org/10.1104/pp.77.4.869openalex-snapshot
Shoot Turgor Does Not Limit Shoot Growth of NaCl-Affected Wheat and Barley
inferred← citeshttps://doi.org/10.1104/pp.91.4.1262openalex-snapshot
Effects of Sodium Chloride on the Hydraulic Conductivity of Soybean Root Systems
inferred← citeshttps://doi.org/10.1104/pp.97.3.1136openalex-snapshot
Effects of Salinity on Water Transport of Excised Maize (Zea mays L.) Roots
inferred← citeshttps://doi.org/10.1111/j.1365-2389.2004.00612.xopenalex-snapshot
Combination of micro suction cups and time‐domain reflectometry to measure osmotic potential gradients between bulk soil and rhizosphere at high resolution in time and space
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1987.tb02076.xopenalex-snapshot
Hydraulic flow characteristics in the lignotuberous mallee Eucalyptus behriana F. Muell. in the field
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1988.tb01147.xopenalex-snapshot
Effect of high external NaCl concentrations on ion transport within the shoot of Lupinus albus. I. Ions in xylem sap
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1988.tb01148.xopenalex-snapshot
Effect of high external NaCl concentration on ion transport within the shoot of Lupinus albus. II. Ions in phloem sap
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1994.tb00262.xopenalex-snapshot
A critical comparison of the pressure‐probe and pressure‐chamber techniques for estimating leaf‐ceil turgor pressure in Kalanchoë daigremontiana
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1994.tb00306.xopenalex-snapshot
Water uptake regulation in peach trees with split‐root systems
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1994.tb02020.xopenalex-snapshot
Replacement of nitrate by ammonium as the nitrogen source increases the salt sensitivity of pea plants. II. Inter‐ and intracellular solute compartmentation in leaflets
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1995.tb00599.xopenalex-snapshot
Xylem pressure response in maize roots subjected to osmotic stress: determination of radial reflection coefficients by use of the xylem pressure probe
inferred← citeshttps://doi.org/10.1111/j.1365-3040.1996.tb00241.xopenalex-snapshot
The water relations of the root–soil interface
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1989.tb05984.xopenalex-snapshot
Growth and root hydraulic conductivity of several citrus rootstocks under salt and polyethylene glycol stresses
inferred← citeshttps://doi.org/10.1111/j.1399-3054.1993.tb08790.xopenalex-snapshot
Cellular responses of two rapid‐cycling Brassica species, B. napus and B. carinata, to seawater salinity
inferred← citeshttps://doi.org/10.1111/j.1399-3054.2006.00633.xopenalex-snapshot
Contrasting water relations of three coastal tree species with different exposure to salinity
inferred← citeshttps://doi.org/10.1111/j.1438-8677.1991.tb00252.xopenalex-snapshot
Ion Transport and the Transpiration Stream
inferred← citeshttps://doi.org/10.1111/j.1438-8677.1994.tb00789.xopenalex-snapshot
High Molecular Weight Organic Compounds in the Xylem Sap of Mangroves: Implications for Long‐Distance Water Transport
inferred← citeshttps://doi.org/10.1111/j.1439-037x.2011.00473.xopenalex-snapshot
Water Relations and Transpiration of Quinoa (Chenopodium quinoa Willd.) Under Salinity and Soil Drying
inferred← citeshttps://doi.org/10.1111/j.1469-8137.1995.tb01811.xopenalex-snapshot
Partitioning and flows of ions and nutrients in salt‐treated plants ofLeptochloa fuscaL. Kunth
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01552.xopenalex-snapshot
Variable tolerance of wetland tree species to combined salinity and waterlogging is related to regulation of ion uptake and production of organic solutes
inferred← citeshttps://doi.org/10.1111/nph.14715openalex-snapshot
Root hairs enable high transpiration rates in drying soils
inferred← citeshttps://doi.org/10.1111/pce.13936openalex-snapshot
Salt stress reduces root water uptake in barley (Hordeum vulgare L.) through modification of the transcellular transport path
inferred← citeshttps://doi.org/10.1177/1934578x211015090openalex-snapshot
Impact of Betaine Under Salinity on Accumulation of Phenolic Compounds in Safflower ( Carthamus tinctorius L.) Sprouts
inferred← citeshttps://doi.org/10.1186/1939-8433-5-11openalex-snapshot
Salinity tolerance mechanisms in glycophytes: An overview with the central focus on rice plants
inferred← citeshttps://doi.org/10.1201/9780824746728.ch40openalex-snapshot
Salt and Drought Stress Effects on Metabolic Regulation in Maize
inferred← citeshttps://doi.org/10.14393/bj-v34n3a2018-38069openalex-snapshot
Effects of NaCl on plant growth and antioxidant activities in fenugreek (Trigonella Foenum Graecum L.)
inferred← citeshttps://doi.org/10.17660/actahortic.2024.1393.37openalex-snapshot
Screening of carrot wild relatives in warm, dry and saline field conditions with respect to root and seed production
inferred← citeshttps://doi.org/10.18016/ksudobil.325374openalex-snapshot
Bazı Tarla Bitkilerinin Tuz Stresine Gösterdikleri Adaptasyon Mekanizmaları
inferred← citeshttps://doi.org/10.2307/2404954openalex-snapshot
Evidence of Water Conservation Mechanisms in Several Subarctic Wetland Species
inferred← citeshttps://doi.org/10.2525/ecb1963.31.147openalex-snapshot
Internal Plant-Water-Status and Its Control. (4) Resistances to Water Flow through Some Root Systems.
inferred← citeshttps://doi.org/10.3126/ijasbt.v4i4.16254openalex-snapshot
Ectopic Overexpression of Barley PIP2;4 Confers Salt Tolerance in Arabidopsis
inferred← citeshttps://doi.org/10.3389/fpls.2019.00080openalex-snapshot
Plant Salinity Stress: Many Unanswered Questions Remain
inferred← citeshttps://doi.org/10.3389/fpls.2022.907937openalex-snapshot
An overview of salinity stress, mechanism of salinity tolerance and strategies for its management in cotton
inferred← citeshttps://doi.org/10.3390/agronomy10020263openalex-snapshot
Grafting Tomato as a Tool to Improve Salt Tolerance
inferred← citeshttps://doi.org/10.3390/agronomy10060906openalex-snapshot
Betaine Hydrochloride Treatment Affects Growth and Phenylpropanoid Accumulation in Tartary Buckwheat (Fagopyrum tataricum) Seedlings under Salt Stress
inferred← citeshttps://doi.org/10.3390/agronomy11081579openalex-snapshot
Abiotic Stress in Plants; Stress Perception to Molecular Response and Role of Biotechnological Tools in Stress Resistance
inferred← citeshttps://doi.org/10.5073/jabfq.2015.088.008openalex-snapshot
Sodium accumulation contributes to salt stress tolerance in lettuce cultivars
inferred← citeshttps://doi.org/10.5772/18580openalex-snapshot
Plant Hydraulic Conductivity: The Aquaporins Contribution
inferred← citeshttps://doi.org/10.5772/intechopen.97664openalex-snapshot
Photosynthetic Antenna Size Regulation as an Essential Mechanism of Higher Plants Acclimation to Biotic and Abiotic Factors: The Role of the Chloroplast Plastoquinone Pool and Hydrogen Peroxide
inferred← citeshttps://doi.org/10.5962/bhl.title.45387openalex-snapshot
Effects of sodium chloride and polyethylene glycol on the water relations, growth, and morphology of citrus rootstock seedlings / by Mongi Zerki.
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.