On the public citation graph
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
0 signed · 100 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known work and none has been retracted — and get a dated CiteStamped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/10.1006/anbo.1996.0405openalex-snapshot
The Use of Agar Nutrient Solution to Simulate Lack of Convection in Waterlogged Soils
inferredcites →https://doi.org/10.1006/anbo.2000.1173openalex-snapshot
Ecophysiology of Wetland Plant Roots: A Modelling Comparison of Aeration in Relation to Species Distribution
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/10.1007/978-3-642-78533-7_17openalex-snapshot
A Microelectrode Study of Oxygen Distribution in the Roots of Intact Maize Seedlings
inferredcites →https://doi.org/10.1016/0304-3770(91)90022-wopenalex-snapshot
Root adaptation to soil waterlogging
inferredcites →https://doi.org/10.1016/0304-3770(96)01044-3openalex-snapshot
Pathways of aeration and the mechanisms and beneficial effects of humidity- and Venturi-induced convections in Phragmites australis (Cav.) Trin. ex Steud.
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/10.1021/je60032a036openalex-snapshot
Diffusion coefficients of nitrogen and oxygen in water
inferredcites →https://doi.org/10.1023/b:rupp.0000003269.31706.edopenalex-snapshot
Exploring the Radial and Longitudinal Aeration of Primary Maize Roots by Means of Clark-Type Oxygen Microelectrodes
inferredcites →https://doi.org/10.1046/j.0016-8025.2001.00817.xopenalex-snapshot
Similarity and diversity in adventitious root anatomy as related to root aeration among a range of wetland and dryland grass species
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/10.1071/fp09144openalex-snapshot
Flooding tolerance: suites of plant traits in variable environments
inferredcites →https://doi.org/10.1071/fp13178openalex-snapshot
Effects of organic acids on the formation of the barrier to radial oxygen loss in roots of Hordeum marinum
inferredcites →https://doi.org/10.1071/fpv44n9_foopenalex-snapshot
Flooding and low oxygen responses in plants
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/mcn142openalex-snapshot
Tolerance of Hordeum marinum accessions to O2 deficiency, salinity and these stresses combined
inferredcites →https://doi.org/10.1093/aob/mct160openalex-snapshot
Flooding tolerance in interspecific introgression lines containing chromosome segments from teosinte (Zea nicaraguensis) in maize (Zea mays subsp. mays)
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/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/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/10.1093/oxfordjournals.pcp.a076248openalex-snapshot
The Remobilization of Nitrogen Related to Leaf Growth and Senescence in Rice Plants (Oryza sativa L.)
inferredcites →https://doi.org/10.1104/pp.17.01157openalex-snapshot
Regulation of Root Traits for Internal Aeration and Tolerance to Soil Waterlogging-Flooding Stress
inferredcites →https://doi.org/10.1104/pp.93.1.271openalex-snapshot
Measurement of Net Fluxes of Ammonium and Nitrate at the Surface of Barley Roots Using Ion-Selective Microelectrodes
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.1365-3040.2011.02318.xopenalex-snapshot
Stagnant deoxygenated growth enhances root suberization and lignifications, but differentially affects water and NaCl permeabilities in rice (Oryza sativa L.) roots
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.1399-3054.1970.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.1399-3054.1975.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.1469-8137.1987.tb00860.xopenalex-snapshot
INTERNAL AERATION AND DEVELOPMENT OF STELA ANOXIA IN SUBMERGED ROOTS
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.1469-8137.2006.01907.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
inferredcites →https://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
inferredcites →https://doi.org/10.1111/nph.13535openalex-snapshot
Oxygen deficiency and salinity affect cell‐specific ion concentrations in adventitious roots of barley ( H ordeum vulgare)
inferredcites →https://doi.org/10.1111/nph.14519openalex-snapshot
Community recommendations on terminology and procedures used in flooding and low oxygen stress research
inferredcites →https://doi.org/10.1111/nph.16368openalex-snapshot
Root O 2 consumption, CO 2 production and tissue concentration profiles in chickpea, as influenced by environmental hypoxia
inferredcites →https://doi.org/10.1111/nph.16375openalex-snapshot
Regulation of root adaptive anatomical and morphological traits during low soil oxygen
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/10.2307/3392992openalex-snapshot
Zea nicaraguensis (Poaceae), a New Teosinte from Pacific Coastal Nicaragua
inferredcites →https://doi.org/10.2307/3558443openalex-snapshot
Rice and Phragmites: effects of organic acids on growth, root permeability, and radial oxygen loss to the rhizosphere
inferredcites →https://doi.org/10.3117/plantroot.1.17openalex-snapshot
Breeding for flooding tolerant maize using "teosinte" as a germplasm resource
inferredcites →https://doi.org/10.3389/fpls.2019.00254openalex-snapshot
Prevention of Radial Oxygen Loss Is Associated With Exodermal Suberin Along Adventitious Roots of Annual Wild Species of Echinochloa
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/pld3.70097openalex-snapshot
Between Two Extremes: Tripsacum dactyloides Root Anatomical Responses to Drought and Waterlogging
inferred← citeshttps://doi.org/10.1007/978-3-031-07434-9_3openalex-snapshot
Future-Proofing Plants Against Climate Change: A Path to Ensure Sustainable Food Systems
inferred← citeshttps://doi.org/10.1007/978-3-031-90617-6_11openalex-snapshot
Current Status and Future Challenges of Nanobiosensors and Nanoformulations in Agriculture
inferred← citeshttps://doi.org/10.1007/978-981-96-8335-2_1openalex-snapshot
Nanobiosensors for Precision Agrobiotechnology
inferred← citeshttps://doi.org/10.1007/978-981-99-9112-9_11openalex-snapshot
Plant Morpho-Physiological Responses to Changes in the Soil Water Status
inferred← citeshttps://doi.org/10.1007/s00468-023-02411-7openalex-snapshot
Resiliency of Nuttall oak but not Shumard oak to winter and spring flood: dormancy alone does not confer flood tolerance
inferred← citeshttps://doi.org/10.1007/s10646-020-02221-4openalex-snapshot
Dynamics of radial oxygen loss in mangroves subjected to waterlogging
inferred← citeshttps://doi.org/10.1007/s11104-022-05364-xopenalex-snapshot
A quantitative review of soybean responses to waterlogging: agronomical, morpho-physiological and anatomical traits of tolerance
inferred← citeshttps://doi.org/10.1007/s11104-022-05711-yopenalex-snapshot
The quantitative importance of key root traits for radial water loss under low water potential
inferred← citeshttps://doi.org/10.1007/s11756-026-02349-4openalex-snapshot
Plant growth regulators as central drivers of waterlogging tolerance: molecular and metabolic perspectives
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.2025.09.001openalex-snapshot
Crop wild relatives: Harnessing ancestral diversity for future food security
inferred← citeshttps://doi.org/10.1016/j.envexpbot.2023.105422openalex-snapshot
A helping hand when drowning: The versatile role of ethylene in root flooding resilience
inferred← citeshttps://doi.org/10.1016/j.plaphy.2026.111668openalex-snapshot
Reduced root lignification resulting from enhanced brassinosteroid signaling compromises waterlogging tolerance in Nardostachys jatamansi seedlings
inferred← citeshttps://doi.org/10.1016/j.stress.2023.100239openalex-snapshot
Nanotechnology based precision agriculture for alleviating biotic and abiotic stress in plants
inferred← citeshttps://doi.org/10.1017/qpb.2025.10016openalex-snapshot
A minimal mechanistic model of plant responses to oxygen deficit during waterlogging
inferred← citeshttps://doi.org/10.1071/fp22294openalex-snapshot
A meta-analysis of plant tissue O2 dynamics
inferred← citeshttps://doi.org/10.1080/1343943x.2025.2590202openalex-snapshot
Potential plant traits and mechanisms behind methane emissions in rice and target genes for further dissection of their roles
inferred← citeshttps://doi.org/10.1093/jxb/eraa175openalex-snapshot
Microsensors in plant biology: in vivo visualization of inorganic analytes with high spatial and/or temporal resolution
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/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/eraf424openalex-snapshot
Maize physiology under waterlogging: shoot and root adaptive responses to mitigate low oxygen stress
inferred← citeshttps://doi.org/10.1093/jxb/erag133openalex-snapshot
Floodproof mustards: adaptation strategies in wild Brassicaceae
inferred← citeshttps://doi.org/10.1093/plcell/koac303openalex-snapshot
Climate change challenges, plant science solutions
inferred← citeshttps://doi.org/10.1093/plphys/kiab392openalex-snapshot
Root plasticity under abiotic stress
inferred← citeshttps://doi.org/10.1093/plphys/kiae586openalex-snapshot
Rooting for survival: how plants tackle a challenging environment through a diversity of root forms and functions
inferred← citeshttps://doi.org/10.1093/treephys/tpae154openalex-snapshot
Willow oak ( Quercus phellos ) seedling roots continue respiration and growth during fall and winter in a soil temperature-dependent manner
inferred← citeshttps://doi.org/10.1093/treephys/tpag002openalex-snapshot
Iron plaque formation confers plant hypoxia tolerance by regulating root oxygen dynamics and respiratory metabolism
inferred← citeshttps://doi.org/10.1111/jipb.13222openalex-snapshot
Water stress resilient cereal crops: Lessons from wild relatives
inferred← citeshttps://doi.org/10.1111/nph.17067openalex-snapshot
Plant performance and food security in a wetter world
inferred← citeshttps://doi.org/10.1111/nph.17326openalex-snapshot
Filling gaps in our understanding of belowground plant traits across the world: an introduction to a Virtual Issue
inferred← citeshttps://doi.org/10.1111/nph.19747openalex-snapshot
Root and shoot phenology, architecture, and organ properties: an integrated trait network among 44 herbaceous wetland species
inferred← citeshttps://doi.org/10.1111/nph.70737openalex-snapshot
Stele tissues of chickpea roots show higher metabolic activity than the cortex, independent of external O 2 supply
inferred← citeshttps://doi.org/10.1111/nph.71593openalex-snapshot
Belowground growth is the primary driver of radial oxygen loss from Typha angustifolia to sediment
inferred← citeshttps://doi.org/10.1111/pce.14270openalex-snapshot
Deconstructing the root system of grasses through an exploration of development, anatomy and function
inferred← citeshttps://doi.org/10.1111/pce.15259openalex-snapshot
Enhanced CO 2 Coordinates the Spatial Recruitment of Diazotrophs in Rice Via Root Development
inferred← citeshttps://doi.org/10.1111/ppl.14216openalex-snapshot
Comparative analysis of defensive secondary metabolites in wild teosinte and cultivated maize under flooding and herbivory stress
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/10.1186/s13068-022-02155-5openalex-snapshot
Physiological and comparative transcriptome analyses reveal the mechanisms underlying waterlogging tolerance in a rapeseed anthocyanin-more mutant
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/10.1270/jsbbs.20117openalex-snapshot
Genetic regulation of root traits for soil flooding tolerance in genus Zea
inferred← citeshttps://doi.org/10.1270/jsbbs.20119openalex-snapshot
Climate-smart crops: key root anatomical traits that confer flooding tolerance
inferred← citeshttps://doi.org/10.1360/ssv-2025-0253openalex-snapshot
Rice plant-mediated methane emissions in paddy fields: a review
inferred← citeshttps://doi.org/10.1360/tb-2022-0669openalex-snapshot
Advances in research and utilization of maize wild relatives
inferred← citeshttps://doi.org/10.15835/nbha49312421openalex-snapshot
Waterlogging tolerance evaluation of fifteen poplar clones cultivated in the Jianghan Plain of China
inferred← citeshttps://doi.org/10.21203/rs.3.rs-1838434/v1openalex-snapshot
The quantitative importance of key root traits on radial water loss
inferred← citeshttps://doi.org/10.3117/plantroot.14.33openalex-snapshot
Formation of a barrier to radial oxygen loss in L-type lateral roots of rice
inferred← citeshttps://doi.org/10.3390/agronomy13051201openalex-snapshot
Role of Exogenous Nitric Oxide in Protecting Plants against Abiotic Stresses
inferred← citeshttps://doi.org/10.3390/f13020324openalex-snapshot
Physiology of Plant Responses to Water Stress and Related Genes: A Review
inferred← citeshttps://doi.org/10.3390/ijms23126383openalex-snapshot
The Role of Phytohormones in Plant Response to Flooding
inferred← citeshttps://doi.org/10.3390/plants10112322openalex-snapshot
Radial Oxygen Loss from Plant Roots—Methods
inferred← citeshttps://doi.org/10.3390/plants11152052openalex-snapshot
Waterlogging Stress Induces Antioxidant Defense Responses, Aerenchyma Formation and Alters Metabolisms of Banana Plants
inferred← citeshttps://doi.org/10.3390/plants13010003openalex-snapshot
Spatial O2 Profile in Coix lacryma-jobi and Sorghum bicolor along the Gas Diffusion Pathway under Waterlogging Conditions
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.