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Rice and Phragmites: effects of organic acids on growth, root permeability, and radial oxygen loss to the rhizosphere

https://doi.org/10.2307/3558443
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What this work says

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

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Visualisation of oxidizing power of rice roots and of possible participation of bacteria in iron deposition
inferredcites →https://doi.org/10.1006/anbo.2000.1236openalex-snapshot
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/bf00003274openalex-snapshot
Vertical profiles of CH4 concentrations, dissolved substrates and processes involved in CH4 production in a flooded Italian rice field
inferredcites →https://doi.org/10.1007/bf00011491openalex-snapshot
Effects of acetic, propionic, and butyric acids on rice seedling growth and nutrition
inferredcites →https://doi.org/10.1007/bf00024600openalex-snapshot
Exchange of trace gases between terrestrial ecosystems and the atmosphere
inferredcites →https://doi.org/10.1007/bf00336255openalex-snapshot
Oxygen profiles and methane turnover in a flooded rice microcosm
inferredcites →https://doi.org/10.1007/bf00336586openalex-snapshot
Methanotrophic bacteria in the rhizosphere of rice microcosms and their effect on porewater methane concentration and methane emission
inferredcites →https://doi.org/10.1007/bf02372636openalex-snapshot
Effects of vegetation on the emission of methane from submerged paddy soil
inferredcites →https://doi.org/10.1007/bf02376798openalex-snapshot
The role of water-soluble components in phytotoxicity from decomposing straw
inferredcites →https://doi.org/10.1007/bf02803996openalex-snapshot
Factors associated with reed decline in a eutrophic fishpond, Rožmberk (South Bohemia, Czech Republic)
inferredcites →https://doi.org/10.1007/bf02804001openalex-snapshot
Effect of nitrogen over-supply on root structure of common reed
inferredcites →https://doi.org/10.1007/bf02804002openalex-snapshot
A role for phytotoxins in thePhragmites die-back syndrome?
inferredcites →https://doi.org/10.1016/0038-0717(78)90083-4openalex-snapshot
Production and phytotoxicity of acetic acid in anaerobic soils containing plant residues
inferredcites →https://doi.org/10.1016/0167-8809(94)00578-3openalex-snapshot
Methane sources and sinks in paddy rice soils: relationship to emissions
inferredcites →https://doi.org/10.1016/0304-3770(93)90040-4openalex-snapshot
Contrasting rates and diurnal patterns of methane emission from emergent aquatic macrophytes
inferredcites →https://doi.org/10.1016/0304-3770(94)90053-1openalex-snapshot
Convective gas flow in Eleocharis sphacelata R. Br.: methane transport and release from wetlands
inferredcites →https://doi.org/10.1016/0304-3770(96)01048-0openalex-snapshot
Control of the diurnal pattern of methane emission from emergent aquatic macrophytes by gas transport mechanisms
inferredcites →https://doi.org/10.1016/0304-3770(96)82384-9openalex-snapshot
Senescence, and phytotoxin, insect, fungal and mechanical damage: factors reducing convective gas-flows in Phragmites australis
inferredcites →https://doi.org/10.1016/b978-0-08-040784-5.50030-9openalex-snapshot
USE OF PHRAGMITES IN SEWAGE SLUDGE TREATMENT
inferredcites →https://doi.org/10.1016/s0304-3770(99)00010-8openalex-snapshot
Methanogenesis and methane emissions: effects of water table, substrate type and presence of Phragmites australis
inferredcites →https://doi.org/10.1016/s0304-3770(99)00058-3openalex-snapshot
Organic acids in the sediments of wetlands dominated by Phragmites australis: evidence of phytotoxic concentrations
inferredcites →https://doi.org/10.1023/a:1005761609386openalex-snapshot
Die-back of Phragmites australis: influence on the distribution and rate of sediment methanogenesis
inferredcites →https://doi.org/10.1029/93jd01667openalex-snapshot
Rhizospheric methane oxidation determined via the methyl fluoride inhibition technique
inferredcites →https://doi.org/10.1029/94gl01595openalex-snapshot
Contribution of photosynthesized carbon to the methane emitted from paddy fields
inferredcites →https://doi.org/10.1038/364794a0openalex-snapshot
Primary production control of methane emission from wetlands
inferredcites →https://doi.org/10.1046/j.1365-3040.1998.00261.xopenalex-snapshot
A comparison of NH4+ and NO3– net fluxes along roots of rice and maize
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00395.xopenalex-snapshot
Phragmites die‐back: toxic effects of propionic, butyric and caproic acids in relation to pH
inferredcites →https://doi.org/10.1080/00380768.1964.10431139openalex-snapshot
Studies on the mechanism of root damage of rice plants in the peat paddy fields (part 1)
inferredcites →https://doi.org/10.1080/00380768.1967.10431969openalex-snapshot
Carbon dioxide and organic acids in relation to the growth of rice
inferredcites →https://doi.org/10.1080/00380768.1968.10432004openalex-snapshot
Studies of the rice plant on an “Akiochi” soil in Korea
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/oso/9780199632046.001.0001openalex-snapshot
Anaerobic Microbiology
inferredcites →https://doi.org/10.1104/pp.46.4.538openalex-snapshot
Effects of Organic Acids on Ion Uptake and Retention in Barley Roots
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.1469-8137.1988.tb04177.xopenalex-snapshot
Phragmites australis– A preliminary study of soil‐oxidizing sites and internal gas transport pathways
inferredcites →https://doi.org/10.1111/j.1469-8137.1992.tb05655.xopenalex-snapshot
Phragmites australis: Venturi‐ and humidity‐induced pressure flows enhance rhizome aeration and rhizosphere oxidation
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03866.xopenalex-snapshot
H+ exchange and nutrient uptake by roots of the emergent hydrophytes, Cyperus involucratus Rottb., Eleocharis sphacelata R. Br. and Juncus ingens N. A. Wakef.
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb02993.xopenalex-snapshot
Root‐induced iron oxidation and pH changes in the lowland rice rhizosphere
inferredcites →https://doi.org/10.1111/j.1469-8137.1995.tb04303.xopenalex-snapshot
Root‐induced solubilization of phosphate in the rhizosphere of lowland rice
inferredcites →https://doi.org/10.1111/j.1469-8137.1996.tb01907.xopenalex-snapshot
Phragmites die–back: bud and root death, blockages within the aeration and vascular systems and the possible role of phytotoxins
inferredcites →https://doi.org/10.1111/j.1469-8137.1996.tb04925.xopenalex-snapshot
Phragmites die‐back: sulphide‐ and acetic acid‐induced bud and root death, lignifications, and blockages within aeration and vascular systems
inferredcites →https://doi.org/10.1139/b89-095openalex-snapshot
Location of radial oxygen loss and zones of potential iron uptake in a grass and two nongrass emergent species
inferredcites →https://doi.org/10.2134/agronj1970.00021962006200030004xopenalex-snapshot
Oxygen Diffusion in the Soil‐Plant System II. Respiration Rate, Permeability, and Porosity of Consecutive Excised Segments of Maize and Rice Roots1
inferredcites →https://doi.org/10.2136/sssaj1999.03615995006300010036xopenalex-snapshot
Iron Oxidation States on Root Surfaces of a Wetland Plant (Phragmites australis)
inferredcites →https://doi.org/10.2307/2261137openalex-snapshot
Conservation and Management of Lakes.
inferredcites →https://doi.org/10.2307/2484860openalex-snapshot
Progress in Phytochemistry.
inferredcites →https://doi.org/10.2307/4040131openalex-snapshot
Mode of Action of Phytotoxic Oils
inferredcites →https://doi.org/10.4319/lo.1989.34.6.1004openalex-snapshot
Nitrification‐denitrification at the plant root‐sediment interface in wetlands

What points at this work

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

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Biochemical Mechanisms of Iron Plaque-Mediated Phosphorus Accumulation and Uptake in Rice Roots
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Effects of Vegetation Removal and Urea Application on Iron and Nitrogen Redox Chemistry in Riparian Forested Soils
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Partial flooding enhances aeration in adventitious roots of black willow (Salix nigra) cuttings
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Effects of organic acids on the formation of the barrier to radial oxygen loss in roots of Hordeum marinum
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Responses of rice to Fe2+ in aerated and stagnant conditions: growth, root porosity and radial oxygen loss barrier
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Outer apoplastic barriers in roots: prospects for abiotic stress tolerance
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Root anatomical plasticity contributes to the different adaptive responses of two Phragmites species to water-deficit and low-oxygen conditions
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Evaluation of Rice Genotypes under Propionate Stress
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Organic Acid Effects on Nutrient Uptake by Rice
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Impact of Roots and Rhizomes on Wetland Archaeology: A Review
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Microstructure, Physical and Mechanical Properties of Adobes Stabilized with Rice Husks
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Microbial colonization in the seagrassPosidoniaspp. roots
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Rice: Sulfide-induced Barriers to Root Radial Oxygen Loss, Fe2+ and Water Uptake, and Lateral Root Emergence
inferred← citeshttps://doi.org/10.1093/aob/mcm236openalex-snapshot
Morphological and Physiological Responses to Sediment Type and Light Availability in Roots of the Submerged Plant Myriophyllum spicatum
inferred← citeshttps://doi.org/10.1093/aob/mcn255openalex-snapshot
Environmental effects on the maturation of the endodermis and multiseriate exodermis of Iris germanica roots
inferred← citeshttps://doi.org/10.1093/aob/mcq221openalex-snapshot
Contrasting dynamics of radial O2-loss barrier induction and aerenchyma formation in rice roots of two lengths
inferred← citeshttps://doi.org/10.1093/aob/mcx047openalex-snapshot
Casparian bands and suberin lamellae in exodermis of lateral roots: an important trait of roots system response to abiotic stress factors
inferred← citeshttps://doi.org/10.1093/jxb/erab043openalex-snapshot
The barrier to radial oxygen loss impedes the apoplastic entry of iron into the roots ofUrochloa humidicola
inferred← citeshttps://doi.org/10.1093/jxb/eraf424openalex-snapshot
Maize physiology under waterlogging: shoot and root adaptive responses to mitigate low oxygen stress
inferred← citeshttps://doi.org/10.1093/jxb/err440openalex-snapshot
Interactions among Fe2+, S2–, and Zn2+ tolerance, root anatomy, and radial oxygen loss in mangrove plants
inferred← citeshttps://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?
inferred← citeshttps://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)
inferred← citeshttps://doi.org/10.1093/plphys/kiae278openalex-snapshot
Low nitrate under waterlogging triggers exodermal suberization to form a barrier to radial oxygen loss in rice roots
inferred← citeshttps://doi.org/10.1093/treephys/tpu042openalex-snapshot
Metal (Pb, Zn and Cu) uptake and tolerance by mangroves in relation to root anatomy and lignification/suberization
inferred← citeshttps://doi.org/10.1099/acmi.0.000114openalex-snapshot
Does salinity affect lifestyle switching in the plant pathogen Fusarium solani?
inferred← citeshttps://doi.org/10.1104/pp.107.102624openalex-snapshot
Effect of Secondary Metabolites Associated with Anaerobic Soil Conditions on Ion Fluxes and Electrophysiology in Barley Roots
inferred← citeshttps://doi.org/10.1104/pp.17.01157openalex-snapshot
Regulation of Root Traits for Internal Aeration and Tolerance to Soil Waterlogging-Flooding Stress
inferred← citeshttps://doi.org/10.1111/1365-2435.13541openalex-snapshot
Drivers of plant traits that allow survival in wetlands
inferred← citeshttps://doi.org/10.1111/fwb.12275openalex-snapshot
Reduced root anchorage of freshwater plants in sandy sediments enriched with fine organic matter
inferred← citeshttps://doi.org/10.1111/fwb.12704openalex-snapshot
Water‐level fluctuations affect sediment properties, carbon flux and growth of the isoetid Littorella uniflora in oligotrophic lakes
inferred← citeshttps://doi.org/10.1111/j.1365-2427.2010.02539.xopenalex-snapshot
Influence of quantity and lability of sediment organic matter on the biomass of two isoetids, Littorella uniflora and Echinodorus repens
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2005.01286.xopenalex-snapshot
Suberin lamella development in maize seedling roots grown in aerated and stagnant conditions
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01434.xopenalex-snapshot
Wound‐induced vascular occlusions in tissues of the reed Phragmites australis: their development and chemical nature
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2006.01878.xopenalex-snapshot
Rhizome phyllosphere oxygenation in Phragmites and other species in relation to redox potential, convective gas flow, submergence and aeration pathways
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2006.01907.xopenalex-snapshot
Apoplastic barriers to radial oxygen loss and solute penetration: a chemical and functional comparison of the exodermis of two wetland species, Phragmites australis and Glyceria maxima
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02467.xopenalex-snapshot
Assessment of O2 diffusivity across the barrier to radial O2 loss in adventitious roots of Hordeum marinum
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03575.xopenalex-snapshot
Physiological and cellular aspects of phytotoxicity tolerance in plants: the role of membrane transporters and implications for crop breeding for waterlogging tolerance
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2007.00373.xopenalex-snapshot
Different bacterial communities associated with the roots and bulk sediment of the seagrass Zostera marina
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2008.00615.xopenalex-snapshot
Structure and function of denitrifying and nitrifying bacterial communities in relation to the plant species in a constructed wetland
inferred← citeshttps://doi.org/10.1111/nph.13124openalex-snapshot
Oxic microshield and local p H enhancement protects Z ostera muelleri from sediment derived hydrogen sulphide
inferred← citeshttps://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
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/nph.17751openalex-snapshot
Abscisic acid is required for exodermal suberization to form a barrier to radial oxygen loss in the adventitious roots of rice (Oryza sativa)
inferred← citeshttps://doi.org/10.1111/nph.18883openalex-snapshot
The barrier to radial oxygen loss protects roots against hydrogen sulphide intrusion and its toxic effect
inferred← citeshttps://doi.org/10.1111/pce.12272openalex-snapshot
Role of root hydrophobic barriers in salt exclusion of a mangrove plant A vicennia officinalis
inferred← citeshttps://doi.org/10.1111/pce.12740openalex-snapshot
Nanoparticle‐based measurements of pH and O2 dynamics in the rhizosphere of Zostera marina L.: effects of temperature elevation and light‐dark transitions
inferred← citeshttps://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
inferred← citeshttps://doi.org/10.1111/pce.14403openalex-snapshot
Beneficial and pathogenic plant‐microbe interactions during flooding stress
inferred← citeshttps://doi.org/10.1111/plb.12014openalex-snapshot
Ethylene – and oxygen signalling – drive plant survival during flooding
inferred← citeshttps://doi.org/10.1111/plb.12398openalex-snapshot
Differential responses of two wetland graminoids to high ammonium at different pH values
inferred← citeshttps://doi.org/10.1111/sum.13024openalex-snapshot
Effect of optimal nitrogen application and mid‐season drainage on rice root activity and reductive substances in straw‐incorporated paddy
inferred← citeshttps://doi.org/10.1186/1939-8433-5-2openalex-snapshot
Mechanisms for coping with submergence and waterlogging in rice
inferred← citeshttps://doi.org/10.1186/s13068-021-01892-3openalex-snapshot
Importance of suberin biopolymer in plant function, contributions to soil organic carbon and in the production of bio-derived energy and materials
inferred← citeshttps://doi.org/10.1264/jsme2.me11314openalex-snapshot
Community Structure and In Situ Activity of Nitrifying Bacteria in Phragmites Root-Associated Biofilms
inferred← citeshttps://doi.org/10.1270/jsbbs.20110openalex-snapshot
A barrier to radial oxygen loss helps the root system cope with waterlogging-induced hypoxia
inferred← citeshttps://doi.org/10.12702/1984-7033.v07n04a07openalex-snapshot
Butyric acid tolerance of rice mutant M4 families
inferred← citeshttps://doi.org/10.1271/kagakutoseibutsu.59.586openalex-snapshot
Molecular Mechanism of Rice Stem Elongation against a Periodic Flood: Stem Elongation in Deepwater Rice
inferred← citeshttps://doi.org/10.1357/002224010793721406openalex-snapshot
Oxygen penetration around burrows and roots in aquatic sediments
inferred← citeshttps://doi.org/10.1371/journal.pone.0098457openalex-snapshot
Spatio-Temporal Patterns in Rhizosphere Oxygen Profiles in the Emergent Plant Species Acorus calamus
inferred← citeshttps://doi.org/10.1371/journal.pone.0129136openalex-snapshot
Sulfide Intrusion and Detoxification in the Seagrass Zostera marina
inferred← citeshttps://doi.org/10.1371/journal.pone.0315657openalex-snapshot
Allelopathic and auto-toxic effects of aqueous extracts of Codonopsis pilosula root secretions
inferred← citeshttps://doi.org/10.1590/1678-4499.166openalex-snapshot
Resposta de plântulas de aveia ao estresse por ácidos acético e butírico
inferred← citeshttps://doi.org/10.1590/s0006-87052009000200006openalex-snapshot
Avaliação de genótipos de aveia branca sob estresse de ácidos orgânicos
inferred← citeshttps://doi.org/10.1590/s0101-31222012000300002openalex-snapshot
Critical levels of organic acids on seed germination and seedling growth of wheat
inferred← citeshttps://doi.org/10.1590/s0102-33062007000100014openalex-snapshot
Níveis críticos dos ácidos acético, propiônico e butírico para estudos de toxicidade em arroz em solução nutritiva
inferred← citeshttps://doi.org/10.1590/s0102-33062010000200027openalex-snapshot
Avaliação de genótipos de arroz sob efeito do ácido butírico
inferred← citeshttps://doi.org/10.1590/s0103-84782008000600014openalex-snapshot
Toxidez por ácido acético em arroz sob diferentes valores de pH da solução nutritiva
inferred← citeshttps://doi.org/10.1590/s0103-84782008005000029openalex-snapshot
Análise da germinação de cultivares de arroz submetidas a estresse por ácido acético
inferred← citeshttps://doi.org/10.1590/s0103-84782010005000083openalex-snapshot
Nível crítico de toxidez do ácido acético em culturas alternativas para solos de várzea
inferred← citeshttps://doi.org/10.1590/s0103-84782013005000090openalex-snapshot
Ácidos orgânicos na qualidade fisiológica de sementes de arroz
inferred← citeshttps://doi.org/10.1590/s1516-89132009000300003openalex-snapshot
Methodology adjustments for organic acid tolerance studies in oat under hydroponic systems
inferred← citeshttps://doi.org/10.1640/0002-8444-104.2.25openalex-snapshot
Cultivation Techniques for Terrestrial Clubmosses (Lycopodiaceae): Conservation, Research, and Horticultural Opportunities for an Early-Diverging Plant Lineage
inferred← citeshttps://doi.org/10.17221/77/2013-swropenalex-snapshot
Interactive effects of arbuscular mycorrhizae and maize (Zea mays L.) straws on wheat (Triticum aestivum L.) growth and organic carbon storage in a sandy loam soil
inferred← citeshttps://doi.org/10.18174/379597openalex-snapshot
Electricity from wetlands : technology assessment of the tubular Plant Microbial Fuel Cell with an integrated biocathode
inferred← citeshttps://doi.org/10.1890/07-0390.1openalex-snapshot
SEPARATING THE EFFECTS OF PARTIAL SUBMERGENCE AND SOIL OXYGEN DEMAND ON PLANT PHYSIOLOGY
inferred← citeshttps://doi.org/10.2134/agronj14.0625openalex-snapshot
Improved Empirical Representation of Plant Responses to Waterlogging for Simulating Crop Yield
inferred← citeshttps://doi.org/10.25959/23239769openalex-snapshot
Improving waterlogging tolerance in barley with molecular and physiological markers
inferred← citeshttps://doi.org/10.3117/rootres.25.47openalex-snapshot
A barrier to radial oxygen loss enables wetland plants to grow under waterlogged conditions
inferred← citeshttps://doi.org/10.33448/rsd-v9i10.8369openalex-snapshot
Evaluation of pre-germinative treatments in seeds of Cereus jamacaru DC subsp. jamacaru (Cactaceae)
inferred← citeshttps://doi.org/10.3354/meps293049openalex-snapshot
Oxic microzones and radial oxygen loss from roots of Zostera marina
inferred← citeshttps://doi.org/10.3389/fpls.2013.00178openalex-snapshot
Does suberin accumulation in plant roots contribute to waterlogging tolerance?
inferred← citeshttps://doi.org/10.3390/f10121131openalex-snapshot
Effects of Salt on Root Aeration, Nitrification, and Nitrogen Uptake in Mangroves
inferred← citeshttps://doi.org/10.3390/ijms22031088openalex-snapshot
Plant Morphological, Physiological and Anatomical Adaption to Flooding Stress and the Underlying Molecular Mechanisms
inferred← citeshttps://doi.org/10.3390/plants11152033openalex-snapshot
The Pyramiding of Three Key Root Traits Aid Breeding of Flood-Tolerant Rice
inferred← citeshttps://doi.org/10.3390/w10060678openalex-snapshot
Constructed Wetlands: A Review on the Role of Radial Oxygen Loss in the Rhizosphere by Macrophytes
inferred← citeshttps://doi.org/10.3390/w15030532openalex-snapshot
Radial Oxygen Loss of Three Plants under Hydroponic Culture and Its Relationships with Pollution Removal
inferred← citeshttps://doi.org/10.3391/ai.2009.4.1.23openalex-snapshot
Preliminary evaluation of effects of invasive tunicate management with acetic acid and calcium hydroxide on non-target marine organisms in Prince Edward Island, Canada
inferred← citeshttps://doi.org/10.3724/sp.j.1258.2012.00982openalex-snapshot
Effects of waterlogging on growth, porosity and radial oxygen loss of three tree species
inferred← citeshttps://doi.org/10.4081/ija.2022.1926openalex-snapshot
Acetic acid disturbs rice germination and post-germination under controlled conditions mimicking green mulching in flooded paddy
inferred← citeshttps://doi.org/10.4161/psb.3.10.6500openalex-snapshot
OutstandingLobelia dortmannain iron armour
inferred← citeshttps://doi.org/10.4161/psb.6.10.17054openalex-snapshot
Casparian strip development and its potential function in salt tolerance
inferred← citeshttps://doi.org/10.5814/j.issn.1674-764x.2025.05.017openalex-snapshot
A Novel in Situ Technique to Map the Distribution of Oxalic Acid in Soil Based on Fluorescence Imaging
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