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Effects of olive root warming on potassium transport and plant growth
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/jpln.200420485openalex-snapshot
The role of potassium in alleviating detrimental effects of abiotic stresses in plants
inferredcites →https://doi.org/10.1007/978-94-010-1009-2openalex-snapshot
Principles of Plant Nutrition
inferredcites →https://doi.org/10.1007/s11104-010-0328-zopenalex-snapshot
The opening of Pandora’s Box: climate change impacts on soil fertility and crop nutrition in developing countries
inferredcites →https://doi.org/10.1016/0098-8472(95)00011-6openalex-snapshot
Methods for reducing the adverse effects of temperature stress on plants: A review
inferredcites →https://doi.org/10.1016/0378-4290(95)90063-2openalex-snapshot
Physiology and determination of crop yield
inferredcites →https://doi.org/10.1016/b978-0-12-473542-2.x5000-7openalex-snapshot
Mineral Nutrition of Higher Plants
inferredcites →https://doi.org/10.1016/j.envexpbot.2007.05.011openalex-snapshot
Heat tolerance in plants: An overview
inferredcites →https://doi.org/10.1016/j.gloplacha.2007.09.005openalex-snapshot
Climate change projections for the Mediterranean region
inferredcites →https://doi.org/10.1016/j.jplph.2007.05.010openalex-snapshot
K+ starvation inhibits water-stress-induced stomatal closure
inferredcites →https://doi.org/10.1016/j.jplph.2013.08.008openalex-snapshot
Potassium in agriculture – Status and perspectives
inferredcites →https://doi.org/10.1016/j.jplph.2013.09.021openalex-snapshot
K+ uptake in plant roots. The systems involved, their regulation and parallels in other organisms
inferredcites →https://doi.org/10.1016/j.jplph.2016.03.001openalex-snapshot
Co-regulation of water and K+ transport in sunflower plants during water stress recovery
inferredcites →https://doi.org/10.1016/j.jplph.2016.10.001openalex-snapshot
Effect of moderate high temperature on the vegetative growth and potassium allocation in olive plants
inferredcites →https://doi.org/10.1016/s0092-8674(00)81606-2openalex-snapshot
Identification and Disruption of a Plant Shaker-like Outward Channel Involved in K+ Release into the Xylem Sap
inferredcites →https://doi.org/10.1042/bst0080235aopenalex-snapshot
Recent Advances in the Biochemistry of Cereals
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00682.xopenalex-snapshot
Kinetics of nutrient uptake by roots: responses to global change
inferredcites →https://doi.org/10.1080/00221589.1976.11514680openalex-snapshot
The Influence of Root Temperature on Apple Trees. I. Growth Responses Related to The Application of Potassium Fertilizer
inferredcites →https://doi.org/10.1080/01904160009382075openalex-snapshot
Root growth and nutrient element status of creeping bentgrass cultivars differing in heat tolerance as influenced by supraoptimal shoot and root temperatures
inferredcites →https://doi.org/10.1093/forestscience/19.2.156openalex-snapshot
Mineral Nutrition of Plants: Principles and Perspectives
inferredcites →https://doi.org/10.1093/jxb/erm284openalex-snapshot
Compatible solute accumulation and stress-mitigating effects in barley genotypes contrasting in their salt tolerance
inferredcites →https://doi.org/10.1093/jxb/ers003openalex-snapshot
Root carbon and protein metabolism associated with heat tolerance
inferredcites →https://doi.org/10.1104/pp.020005openalex-snapshot
Turgor Regulation in Osmotically Stressed Arabidopsis Epidermal Root Cells. Direct Support for the Role of Inorganic Ion Uptake as Revealed by Concurrent Flux and Cell Turgor Measurements
inferredcites →https://doi.org/10.1104/pp.67.4.815openalex-snapshot
Temperature Dependence of the Concentration Kinetics of Absorption of Phosphate and Potassium in Corn Roots
inferredcites →https://doi.org/10.1104/pp.90.3.939openalex-snapshot
Two Modes of Rubidium Uptake in Sunflower Plants
inferredcites →https://doi.org/10.1105/tpc.12.4.479openalex-snapshot
Heat Shock Protein 101 Plays a Crucial Role in Thermotolerance in Arabidopsis
inferredcites →https://doi.org/10.1111/j.1365-3040.2011.02426.xopenalex-snapshot
ABA signal transduction at the crossroad of biotic and abiotic stress responses
inferredcites →https://doi.org/10.1111/j.1399-3054.1978.tb01599.xopenalex-snapshot
Rapid Effects of Abscisic Acid on Ion Uptake in Sunflower Roots
inferredcites →https://doi.org/10.1111/j.1399-3054.1980.tb03332.xopenalex-snapshot
Effects of potassium and gibberellic acid on stem growth of whole sunflower plants
inferredcites →https://doi.org/10.1111/j.1399-3054.1982.tb00699.xopenalex-snapshot
Effect of potassium on the water potential, the pressure potential, the osmotic potential and cell elongation in leaves of Phaseolus vulgaris
inferredcites →https://doi.org/10.1111/j.1399-3054.1985.tb01899.xopenalex-snapshot
Effect of potassium status on K+ (Rb)+ uptake and transport in sunflower roots
inferredcites →https://doi.org/10.1111/j.1399-3054.2006.00709.xopenalex-snapshot
Co‐regulation of water channels and potassium channels in rice
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03760.xopenalex-snapshot
Effects of soil temperature and nitrogen status on kinetics of 15NO3− uptake by roots of field‐grown Agropyron desertorum (Fisch. ex Link) Schult
inferredcites →https://doi.org/10.1146/annurev.arplant.37.1.363openalex-snapshot
Alteration of Gene Expression During Environmental Stress in Plants
inferredcites →https://doi.org/10.1146/annurev.arplant.54.031902.134831openalex-snapshot
Molecular Mechanisms and Regulation of K + Transport in Higher Plants
inferredcites →https://doi.org/10.1146/annurev.pp.37.060186.002051openalex-snapshot
Alteration of Gene Expression During Environmental Stress in Plants
inferredcites →https://doi.org/10.1175/bams-d-11-00136.1openalex-snapshot
The CIRCE Simulations: Regional Climate Change Projections with Realistic Representation of the Mediterranean Sea
inferredcites →https://doi.org/10.21273/jashs.115.6.1008openalex-snapshot
14Carbon-labeled Photosynthate Partitioning in Ilex crenata `Rotundifolia' at Supraoptimal Root-zone Temperatures
inferredcites →https://doi.org/10.2134/1994.physiologyanddetermination.c25openalex-snapshot
High Temperature Responses of Crop Plants
inferredcites →https://doi.org/10.2134/asaspecpub49.c1openalex-snapshot
Mechanisms of Nutrient Fluxes at Membranes of the Root Surface and their Regulation in the Whole Plant
inferredcites →https://doi.org/10.2135/cropsci1995.0011183x003500020034xopenalex-snapshot
Root Cytokinin Level in Relation to Heat Tolerance of Phaseolus acutifolius and Phaseolus vulgaris
inferredcites →https://doi.org/10.2135/cropsci2000.4051363xopenalex-snapshot
Growth and Physiological Responses of Creeping Bentgrass to Changes in Air and Soil Temperatures
inferredcites →https://doi.org/10.2135/cropsci2000.4051368xopenalex-snapshot
Effects of Differential Air and Soil Temperature on Carbohydrate Metabolism in Creeping Bentgrass
inferredcites →https://doi.org/10.2136/sssaj1972.03615995003600060002xopenalex-snapshot
Recent Advances in Plant Nutrition
inferredcites →https://doi.org/10.2136/sssaj1999.03615995006300030021xopenalex-snapshot
Soil Temperature, Matric Potential, and the Kinetics of Microbial Respiration and Nitrogen Mineralization
inferredcites →https://doi.org/10.2307/1935449openalex-snapshot
Morphological and Physiological Mechanisms of Temperature Compensation in Phosphate Absorption along a Latitudinal Gradient
inferredcites →https://doi.org/10.3389/fpls.2012.00167openalex-snapshot
Phylogenetic Analysis of K+ Transporters in Bryophytes, Lycophytes, and Flowering Plants Indicates a Specialization of Vascular Plants
inferredcites →https://doi.org/10.3389/fpls.2013.00224openalex-snapshot
The role of K+ channels in uptake and redistribution of potassium in the model plant Arabidopsis thaliana
inferredcites →https://doi.org/10.3390/plants6010006openalex-snapshot
Heat Stress Decreases Levels of Nutrient-Uptake and -Assimilation Proteins in Tomato Roots
inferredcites →https://doi.org/10.5860/choice.45-5008openalex-snapshot
IPCC--Intergovernmental Panel on Climate Change
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4782305openalex-extracted
Tamyb-Cc5 Gene Specifically Expressed in Root Improve Tolerance of Phosphorus Deficiency and Drought Stress in Wheat
inferred← citeshttps://doi.org/10.1007/s00344-021-10399-yopenalex-snapshot
Application of Exogenous KH2PO4 and Salicylic Acid and Optimization of the Sowing Date Enhance Rice Yield Under High-Temperature Conditions
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2023.138576openalex-snapshot
Impact of nanopesticide CuO-NPs and nanofertilizer CeO2-NPs on wheat Triticum aestivum under global warming scenarios
inferred← citeshttps://doi.org/10.1016/j.marpolbul.2022.113717openalex-snapshot
Root growth and architecture of Tamarix chinensis in response to the groundwater level in the Yellow River Delta
inferred← citeshttps://doi.org/10.1016/j.plaphy.2023.107986openalex-snapshot
Morphological, physiological and metabolomic analysis to unravel the adaptive relationship between root growth of ephemeral plants and different soil habitats
inferred← citeshttps://doi.org/10.1016/j.plaphy.2024.109011openalex-snapshot
TaMYB-CC5 gene specifically expressed in root improve tolerance of phosphorus deficiency and drought stress in wheat
inferred← citeshttps://doi.org/10.1016/j.scienta.2019.01.046openalex-snapshot
Global warming effects on yield and fruit maturation of olive trees growing under field conditions
inferred← citeshttps://doi.org/10.1016/j.scienta.2023.111956openalex-snapshot
Effect of low root-zone temperature on photosynthesis, root structure and mineral element absorption of tomato seedlings
inferred← citeshttps://doi.org/10.1111/ajgw.12550openalex-snapshot
Rootstock type influences salt exclusion response of grafted Shiraz under salt treatment at elevated root zone temperature
inferred← citeshttps://doi.org/10.12677/ije.2021.104068openalex-snapshot
Effects of Nitrogen Increase and Precipitation Changes on Early Spring Plants under Global Climate Change: A Review
inferred← citeshttps://doi.org/10.32615/bp.2021.070openalex-snapshot
Effects of high growth-medium temperature under controlled conditions on characteristics of tomato leaves
inferred← citeshttps://doi.org/10.3389/fpls.2021.796956openalex-snapshot
Enhanced Flavonoid Accumulation Reduces Combined Salt and Heat Stress Through Regulation of Transcriptional and Hormonal Mechanisms
inferred← citeshttps://doi.org/10.3389/fpls.2024.1410036openalex-snapshot
Root growth characteristics and antioxidant system of Suaeda salsa in response to the short-term nitrogen and phosphorus addition in the Yellow River Delta
inferred← citeshttps://doi.org/10.3389/fpls.2026.1941938openalex-snapshot
Cultivar-specific coordination of root plasticity and root antioxidant defense underlies drought adaptation in alfalfa
inferred← citeshttps://doi.org/10.3390/agronomy10060805openalex-snapshot
Fractal and Topological Analyses and Antioxidant Defense Systems of Alfalfa (Medicago sativa L.) Root System under Drought and Rehydration Regimes
inferred← citeshttps://doi.org/10.3390/ijms20030715openalex-snapshot
The Complex Fine-Tuning of K+ Fluxes in Plants in Relation to Osmotic and Ionic Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/plants10020419openalex-snapshot
Potassium Control of Plant Functions: Ecological and Agricultural Implications
inferred← citeshttps://doi.org/10.3390/plants12051163openalex-snapshot
Metabolomic Analysis of Key Metabolites and Their Pathways Revealed the Response of Alfalfa (Medicago sativa L.) Root Exudates to rac-GR24 under Drought Stress
inferred← citeshttps://doi.org/10.3390/plants12142737openalex-snapshot
Effects of Harvesting Time on Fruit Development Process and Oil Content of Selected Iranian and Foreign Olive Cultivars under Subtropical Conditions
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