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Radial Oxygen Loss from Plant Roots—Methods

https://doi.org/10.3390/plants10112322
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

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Oxygen Distribution in Wetland Plant Roots and Permeability Barriers to Gas-exchange with the Rhizosphere: a Microelectrode and Modelling Study with Phragmites australis
inferredcites →https://doi.org/10.1007/s11104-005-0462-1openalex-snapshot
A Method to Estimate Practical Radial Oxygen Loss of Wetland Plant Roots
inferredcites →https://doi.org/10.1007/s11104-010-0637-2openalex-snapshot
Monitoring of root growth and redox conditions in paddy soil rhizotrons by redox electrodes and image analysis
inferredcites →https://doi.org/10.1007/s11104-015-2382-zopenalex-snapshot
O2 dynamics in the rhizosphere of young rice plants (Oryza sativa L.) as studied by planar optodes
inferredcites →https://doi.org/10.1007/s12566-012-0032-yopenalex-snapshot
Indicators for optical oxygen sensors
inferredcites →https://doi.org/10.1016/b978-0-08-040784-5.50009-7openalex-snapshot
MEASUREMENT AND MODELLING OF OXYGEN RELEASE FROM ROOTS OF PHRAGMITES AUSTRALIS
inferredcites →https://doi.org/10.1016/j.aca.2015.02.006openalex-snapshot
Two decades of chemical imaging of solutes in sediments and soils – a review
inferredcites →https://doi.org/10.1016/j.jplph.2019.04.010openalex-snapshot
Tolerance of roots to low oxygen: ‘Anoxic’ cores, the phytoglobin-nitric oxide cycle, and energy or oxygen sensing
inferredcites →https://doi.org/10.1016/s0065-2113(08)60633-1openalex-snapshot
The Chemistry of Submerged Soils
inferredcites →https://doi.org/10.1016/s0065-2296(08)60089-0openalex-snapshot
Aeration in Higher Plants
inferredcites →https://doi.org/10.1016/s0925-4005(98)00232-9openalex-snapshot
A modular luminescence lifetime imaging system for mapping oxygen distribution in biological samples
inferredcites →https://doi.org/10.1021/acs.estlett.9b00403openalex-snapshot
Iron Lung: How Rice Roots Induce Iron Redox Changes in the Rhizosphere and Create Niches for Microaerophilic Fe(II)-Oxidizing Bacteria
inferredcites →https://doi.org/10.1021/acssensors.0c02084openalex-snapshot
Hyperspectral Luminescence Imaging in Combination with Signal Deconvolution Enables Reliable Multi-Indicator-Based Chemical Sensing
inferredcites →https://doi.org/10.1021/es501127kopenalex-snapshot
Localized Flux Maxima of Arsenic, Lead, and Iron around Root Apices in Flooded Lowland Rice
inferredcites →https://doi.org/10.1021/es505734bopenalex-snapshot
Optical Sensor Nanoparticles in Artificial Sediments–A New Tool To Visualize O2 Dynamics around the Rhizome and Roots of Seagrasses
inferredcites →https://doi.org/10.1023/a:1003052226202openalex-snapshot
Macrophyte development and resuspension regulate the photosynthesis and production of benthic microalgae
inferredcites →https://doi.org/10.1038/204801b0openalex-snapshot
Oxygen Diffusion from the Roots of Some British Bog Plants
inferredcites →https://doi.org/10.1038/s41396-018-0308-5openalex-snapshot
Oxygen loss from seagrass roots coincides with colonisation of sulphide-oxidising cable bacteria and reduces sulphide stress
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00317.xopenalex-snapshot
Development of anatomical structure of roots of Phragmites australis
inferredcites →https://doi.org/10.1046/j.1365-3040.1999.00517.xopenalex-snapshot
Effect of external oxygen demand on radial oxygen loss by Juncus roots in titanium citrate solutions
inferredcites →https://doi.org/10.1046/j.1365-3040.2003.00846.xopenalex-snapshot
Long‐distance transport of gases in plants: a perspective on internal aeration and radial oxygen loss from roots
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00793.xopenalex-snapshot
Rice root properties for internal aeration and efficient nutrient acquisition in submerged soil
inferredcites →https://doi.org/10.1071/fp02081openalex-snapshot
Spatial patterns of radial oxygen loss and nitrate net flux along adventitious roots of rice raised in aerated or stagnant solution
inferredcites →https://doi.org/10.1071/fp13359openalex-snapshot
Responses of rice to Fe2+ in aerated and stagnant conditions: growth, root porosity and radial oxygen loss barrier
inferredcites →https://doi.org/10.1071/fp14078openalex-snapshot
Radial oxygen loss and physical barriers in relation to root tissue age in species with different types of aerenchyma
inferredcites →https://doi.org/10.1071/fp16327openalex-snapshot
Anatomical and biochemical characterisation of a barrier to radial O2 loss in adventitious roots of two contrasting Hordeum marinum accessions
inferredcites →https://doi.org/10.1071/pp97135openalex-snapshot
Response to oxygen deficiency in primary maize roots. I. Development of oxygen deficiency in the stele reduces radial solute transport to the xylem
inferredcites →https://doi.org/10.1080/17451000801888726openalex-snapshot
Oxygen dynamics of marine sediments
inferredcites →https://doi.org/10.1093/aob/mcf114openalex-snapshot
Aerenchyma and an Inducible Barrier to Radial Oxygen Loss Facilitate Root Aeration in Upland, Paddy and Deep-water Rice (Oryza sativa L.)
inferredcites →https://doi.org/10.1093/aob/mci215openalex-snapshot
Rice: Sulfide-induced Barriers to Root Radial Oxygen Loss, Fe2+ and Water Uptake, and Lateral Root Emergence
inferredcites →https://doi.org/10.1093/aob/mcq221openalex-snapshot
Contrasting dynamics of radial O2-loss barrier induction and aerenchyma formation in rice roots of two lengths
inferredcites →https://doi.org/10.1093/aob/mcz071openalex-snapshot
Root-zone hypoxia reduces growth of the tropical forage grass Urochloa humidicola in high-nutrient but not low-nutrient conditions
inferredcites →https://doi.org/10.1093/jexbot/49.325.1431openalex-snapshot
The barrier to radial oxygen loss from roots of rice (Oryza sativa L.) is induced by growth in stagnant solution
inferredcites →https://doi.org/10.1093/jxb/eraa175openalex-snapshot
Microsensors in plant biology: in vivo visualization of inorganic analytes with high spatial and/or temporal resolution
inferredcites →https://doi.org/10.1093/jxb/erab043openalex-snapshot
The barrier to radial oxygen loss impedes the apoplastic entry of iron into the roots ofUrochloa humidicola
inferredcites →https://doi.org/10.1093/jxb/ern300openalex-snapshot
Measurements of oxygen permeability coefficients of rice (Oryza sativa L.) roots using a new perfusion technique
inferredcites →https://doi.org/10.1093/jxb/erp089openalex-snapshot
Functional and chemical comparison of apoplastic barriers to radial oxygen loss in roots of rice (Oryza sativa L.) grown in aerated or deoxygenated solution
inferredcites →https://doi.org/10.1093/jxb/erq271openalex-snapshot
Ion transport in seminal and adventitious roots of cereals during O2 deficiency
inferredcites →https://doi.org/10.1093/jxb/ers017openalex-snapshot
Do radial oxygen loss and external aeration affect iron plaque formation and arsenic accumulation and speciation in rice?
inferredcites →https://doi.org/10.1093/jxb/eru235openalex-snapshot
Microarray analysis of laser-microdissected tissues indicates the biosynthesis of suberin in the outer part of roots during formation of a barrier to radial oxygen loss in rice (Oryza sativa)
inferredcites →https://doi.org/10.1104/pp.99.2.734openalex-snapshot
Measurement of Net Fluxes of Ammonium and Nitrate at the Surface of Barley Roots Using Ion-Selective Microelectrodes
inferredcites →https://doi.org/10.1111/j.1365-2389.1967.tb01483.xopenalex-snapshot
THE RELATIONSHIP BETWEEN OXIDATION‐REDUCTION POTENTIALS AND OXYGEN‐DIFFUSION LEVELS IN SOME WATERLOGGED ORGANIC SOILS
inferredcites →https://doi.org/10.1111/j.1365-3040.2012.02513.xopenalex-snapshot
Enhanced formation of aerenchyma and induction of a barrier to radial oxygen loss in adventitious roots of Zea nicaraguensis contribute to its waterlogging tolerance as compared with maize ( Zea mays ssp. mays )
inferredcites →https://doi.org/10.1111/j.1399-3054.1967.tb08379.xopenalex-snapshot
The Oxidising Activity of Roots in Waterlogged Soils
inferredcites →https://doi.org/10.1111/j.1399-3054.1970.tb06455.xopenalex-snapshot
Rhizosphere Oxidation in Rice and other Species: A Mathematical Model Based on the Oxygen Flux Component
inferredcites →https://doi.org/10.1111/j.1399-3054.1971.tb01427.xopenalex-snapshot
Radial Oxygen Losses from Intact Rice Roots as Affected by Distance from the Apex, Respiration and Waterlogging
inferredcites →https://doi.org/10.1111/j.1399-3054.1975.tb03861.xopenalex-snapshot
Radial Oxygen Loss from Roots: The Theoretical Basis for the Manipulation of Flux Data Obtained by the Cylindrical Platinum Electrode Technique
inferredcites →https://doi.org/10.1111/j.1469-8137.1983.tb04864.xopenalex-snapshot
OXYGEN DIFFUSION IN PEA II. OXYGEN CONCENTRATIONS IN THE PRIMARY PEA ROOT APEX AS AFFECTED BY GROWTH, THE PRODUCTION OF LATERALS AND RADIAL OXYGEN LOSS
inferredcites →https://doi.org/10.1111/j.1469-8137.1988.tb04177.xopenalex-snapshot
Phragmites australis– A preliminary study of soil‐oxidizing sites and internal gas transport pathways
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01725.xopenalex-snapshot
Root aeration in rice (Oryza sativa): evaluation of oxygen, carbon dioxide, and ethylene as possible regulators of root acclimatizations
inferredcites →https://doi.org/10.1111/nph.16452openalex-snapshot
Lateral roots, in addition to adventitious roots, form a barrier to radial oxygen loss in Zea nicaraguensis and a chromosome segment introgression line in maize
inferredcites →https://doi.org/10.1111/nph.17474openalex-snapshot
Novel functions of the root barrier to radial oxygen loss – radial diffusion resistance to H 2 and water vapour
inferredcites →https://doi.org/10.1111/pce.12294openalex-snapshot
Biochemical and molecular characterization of rice ( O ryza sativa L .) roots forming a barrier to radial oxygen loss
inferredcites →https://doi.org/10.1111/pce.12849openalex-snapshot
A major locus involved in the formation of the radial oxygen loss barrier in adventitious roots of teosinte Zea nicaraguensis is located on the short‐arm of chromosome 3
inferredcites →https://doi.org/10.1111/pce.13562openalex-snapshot
Rice acclimation to soil flooding: Low concentrations of organic acids can trigger a barrier to radial oxygen loss in roots
inferredcites →https://doi.org/10.1111/pce.13638openalex-snapshot
Soil carbon dioxide venting through rice roots
inferredcites →https://doi.org/10.1366/0003702001949726openalex-snapshot
Luminescence Lifetime Imaging of Oxygen, pH, and Carbon Dioxide Distribution Using Optical Sensors
inferredcites →https://doi.org/10.2134/agronj1994.00021962008600030005xopenalex-snapshot
A Colorimetric Method for Assaying Dissolved Oxygen Loss from Container‐Grown Rice Roots
inferredcites →https://doi.org/10.3117/plantroot.14.33openalex-snapshot
Formation of a barrier to radial oxygen loss in L-type lateral roots of rice
inferredcites →https://doi.org/10.3354/meps11041openalex-snapshot
Rhizosphere O2 dynamics in young Zostera marina and Ruppia maritima
inferredcites →https://doi.org/10.3354/meps140217openalex-snapshot
Planar optrodes:a new tool for fine scale measurements of two-dimensional O2 distribution in benthic communities
inferredcites →https://doi.org/10.3354/meps293049openalex-snapshot
Oxic microzones and radial oxygen loss from roots of Zostera marina
inferredcites →https://doi.org/10.3389/fpls.2019.00259openalex-snapshot
Root Cortex Provides a Venue for Gas-Space Formation and Is Essential for Plant Adaptation to Waterlogging
inferredcites →https://doi.org/10.3390/plants9070880openalex-snapshot
Some Accessions of Amazonian Wild Rice (Oryza glumaepatula) Constitutively Form a Barrier to Radial Oxygen Loss along Adventitious Roots under Aerated Conditions
inferredcites →https://doi.org/10.4319/lo.1989.34.2.0474openalex-snapshot
An oxygen microsensor with a guard cathode
inferredcites →https://doi.org/10.4319/lo.1995.40.6.1159openalex-snapshot
Fiber‐optic oxygen microsensors, a new tool in aquatic biology
inferredcites →https://doi.org/10.4319/lo.1998.43.8.1932openalex-snapshot
Predicting the signal of O2 microsensors from physical dimensions, temperature, salinity, and O2 concentration
inferredcites →https://doi.org/10.4319/lo.2001.46.8.2073openalex-snapshot
An in situ instrument for planar O2 optode measurements at benthic interfaces
inferredcites →https://doi.org/10.4319/lo.2006.51.2.1072openalex-snapshot
Oxygen dynamics in the rhizosphere of Zostera marina: A two-dimensional planar optode study
inferredcites →https://doi.org/10.4319/lom.2010.8.254openalex-snapshot
A novel planar optode setup for concurrent oxygen and light field imaging: Application to a benthic phototrophic community
inferredcites →https://doi.org/10.4319/lom.2011.9.348openalex-snapshot
A simple and inexpensive high resolution color ratiometric planar optode imaging approach: application to oxygen and pH sensing.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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Optimizing the Early Stages of Cw-Mfc Lifecycle: A Guide to Plant Selection, Acclimation, and Start-Up
inferred← citeshttps://doi.org/10.1007/978-981-99-9112-9_8openalex-snapshot
Development and Regulation of a Radial Oxygen Loss Barrier to Acclimate to Anaerobic Conditions
inferred← citeshttps://doi.org/10.1007/s00344-026-12139-6openalex-snapshot
Yield and Essential Oil Accumulation of Stachys setifera Linked to Aerenchyma Development
inferred← citeshttps://doi.org/10.1007/s11104-026-09018-0openalex-snapshot
Spatiotemporal dynamics of radial oxygen loss during rice seedling establishment in a stagnant deoxygenated agar medium
inferred← citeshttps://doi.org/10.1016/b978-0-12-819773-8.00001-0openalex-snapshot
Plant responses to soil-borne ion toxicities
inferred← citeshttps://doi.org/10.1016/j.cj.2026.01.007openalex-snapshot
Root cortical senescence: An adaptive mechanism for drought tolerance in crops
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105941openalex-snapshot
Silicon weakens the outer apoplastic barrier in roots of rice and delays its formation, resulting in increased Na+ and Cl− fluxes to the shoot
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2024.105990openalex-snapshot
The role of cytokinins during flooding stress in plants
inferred← citeshttps://doi.org/10.1016/j.flora.2025.152674openalex-snapshot
High-resolution characterization of rhizosphere oxygen (O2) dynamics in different wetland plant species after light/dark transitions
inferred← citeshttps://doi.org/10.1016/j.geoderma.2025.117658openalex-snapshot
Root organic exudate stimulation of greenhouse gases is offset by radial oxygen loss in mineral-dominated anoxic wetland soil
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131006openalex-snapshot
Sediment arsenic remediation by submerged macrophytes via root-released O2 and microbe-mediated arsenic biotransformation
inferred← citeshttps://doi.org/10.1016/j.jhazmat.2023.131580openalex-snapshot
High-resolution imaging of O2 dynamics and metal solubilization in the rhizosphere of the hyperaccumulator Leersia hexandra Swartz
inferred← citeshttps://doi.org/10.1016/j.marchem.2026.104661openalex-snapshot
Multi-parameter imaging with planar optodes and 2D DET hydrogels: Application in the rhizosphere of seagrass (Z. marina)
inferred← citeshttps://doi.org/10.1016/j.ocecoaman.2026.108176openalex-snapshot
Mitigation of sulfide stress on eelgrass Zostera marina and Manila clam Ruditapes philippinarum through an eelgrass–clam coculture system
inferred← citeshttps://doi.org/10.1016/j.soilbio.2025.109947openalex-snapshot
Carbon stabilization by iron plaque on rice roots: The role of oxygen loss
inferred← citeshttps://doi.org/10.1016/j.soilbio.2025.110036openalex-snapshot
The influence of iron plaque and root traits on organic carbon turnover in the rice root detritusphere
inferred← citeshttps://doi.org/10.1038/s43247-025-03163-7openalex-snapshot
Optimized wetland rewetting strategies can control methane, carbon dioxide, and oxygen responses to water table fluctuations
inferred← citeshttps://doi.org/10.1071/fp22294openalex-snapshot
A meta-analysis of plant tissue O2 dynamics
inferred← citeshttps://doi.org/10.1080/10643389.2022.2164154openalex-snapshot
Metals in coastal seagrass habitats: A systematic quantitative literature review
inferred← citeshttps://doi.org/10.1093/aob/mcae036openalex-snapshot
Function and induction of the root barrier to radial O2 loss. A commentary on ‘Exogenous abscisic acid induces the formation of a suberized barrier to radial oxygen loss in adventitious roots of barley (Hordeum vulgare)’
inferred← citeshttps://doi.org/10.1093/aob/mcae131openalex-snapshot
Anatomical and physiological responses of roots and rhizomes in Oryza longistaminata to soil water gradients
inferred← citeshttps://doi.org/10.1093/jxb/erad014openalex-snapshot
Responses of key root traits in the genusOryzato soil flooding mimicked by stagnant, deoxygenated nutrient solution
inferred← citeshttps://doi.org/10.1093/jxb/erag030openalex-snapshot
Oxygen consumption and diffusional resistance both determine maximum root length in flooded soils
inferred← citeshttps://doi.org/10.1093/plphys/kiae458openalex-snapshot
Leaf Gas Film 1 promotes glycerol ester accumulation and formation of a tight root barrier to radial O2 loss in rice
inferred← citeshttps://doi.org/10.1093/plphys/kiae623openalex-snapshot
Designed to breathe: synthetic biology applications in plant hypoxia
inferred← citeshttps://doi.org/10.1093/plphys/kiae624openalex-snapshot
Tools to understand hypoxia responses in plant tissues
inferred← citeshttps://doi.org/10.1093/plphys/kiag675openalex-snapshot
Characterization of rhizosphere oxidation associated with root development in rice using planar oxygen optodes
inferred← citeshttps://doi.org/10.1111/nph.71549openalex-snapshot
Radial oxygen loss, rhizospheric methane oxidation and methane emissions from rice roots
inferred← citeshttps://doi.org/10.1111/pce.15319openalex-snapshot
Formation of Apoplastic Barriers to Radial O₂ Loss in Rice Roots: Effects of Low‐O₂ and High‐Fe Conditions, and the Roles of Suberin, Glycerol Esters, and Iron Plaques
inferred← citeshttps://doi.org/10.1177/15579018261461317openalex-snapshot
Degradable Versus Nondegradable Microplastics: Impacts on Plant Growth, Radial Oxygen Loss, and Soil Microbial Associations of Canna indica
inferred← citeshttps://doi.org/10.1186/s12284-023-00638-zopenalex-snapshot
Mitigation of Greenhouse Gas Emissions from Rice via Manipulation of Key Root Traits
inferred← citeshttps://doi.org/10.12677/gser.2026.153057openalex-snapshot
Research Progress on the Effects of Vegetation Restoration in Lake Wetlands on Sediment Carbon and Nitrogen Cycling and Ecosystem Functions
inferred← citeshttps://doi.org/10.3389/fbioe.2024.1276176openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/plants13010003openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/polym14204448openalex-snapshot
On the Use of Polymer-Based Composites for the Creation of Optical Sensors: A Review
inferred← citeshttps://doi.org/10.3390/w18182282openalex-snapshot
Root Oxygen Microzones and Nitrogen Cycling in Constructed Wetlands: A Mechanistic Review of Radial Oxygen Loss, Pathway Partitioning, and Scale-Bridging
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