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Mechanisms for tolerance of very high tissue phosphorus concentrations in P tilotus polystachyus
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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/jemt.1070280108openalex-snapshot
Planing frozen hydrated plant specimens for SEM observation and EDX microanalysis
inferredcites →https://doi.org/10.1007/bf02181879openalex-snapshot
The availability of P from phosphate-goethite bridging complexes. Desorption and uptake by ryegrass
inferredcites →https://doi.org/10.1007/s11104-004-2725-7openalex-snapshot
Cluster Roots: A Curiosity in Context
inferredcites →https://doi.org/10.1007/s11104-009-0088-9openalex-snapshot
Variation in seedling growth of 11 perennial legumes in response to phosphorus supply
inferredcites →https://doi.org/10.1007/s11104-009-0249-xopenalex-snapshot
Variation in morphological and physiological parameters in herbaceous perennial legumes in response to phosphorus supply
inferredcites →https://doi.org/10.1007/s11104-011-0880-1openalex-snapshot
Strategies and agronomic interventions to improve the phosphorus-use efficiency of farming systems
inferredcites →https://doi.org/10.1007/s11104-012-1311-7openalex-snapshot
Growth, carboxylate exudates and nutrient dynamics in three herbaceous perennial plant species under low, moderate and high phosphorus supply
inferredcites →https://doi.org/10.1016/j.envexpbot.2007.03.004openalex-snapshot
Seedling response to phosphate addition and inoculation with arbuscular mycorrhizas and the implications for old-field restoration in Western Australia
inferredcites →https://doi.org/10.1016/j.envpol.2006.06.006openalex-snapshot
Phytoextraction of excess soil phosphorus
inferredcites →https://doi.org/10.1016/j.gloenvcha.2008.10.009openalex-snapshot
The story of phosphorus: Global food security and food for thought
inferredcites →https://doi.org/10.1016/j.scienta.2008.05.001openalex-snapshot
Phosphorus toxicity in the Proteaceae: A problem in post-agricultural lands
inferredcites →https://doi.org/10.1016/j.tree.2008.11.009openalex-snapshot
Eutrophication science: where do we go from here?
inferredcites →https://doi.org/10.1039/an9830800361openalex-snapshot
Spectrophotometric determination of phosphate in river waters with molybdate and malachite green
inferredcites →https://doi.org/10.1046/j.1365-2818.2000.00679.xopenalex-snapshot
The reliability of cryoSEM for the observation and quantification of xylem embolisms and quantitative analysis of xylem sap in situ
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00695.xopenalex-snapshot
Phosphorus acquisition and use: critical adaptations by plants for securing a nonrenewable resource
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00884.xopenalex-snapshot
Location and quantification of phosphorus and other elements in fully hydrated, soil‐grown arbuscular mycorrhizas: a cryo‐analytical scanning electron microscopy study
inferredcites →https://doi.org/10.1071/ea98133openalex-snapshot
Phosphorus availability and the growth, mineral composition and nutritive value of ephemeral forbs and associated perennials from the Pilbara, Western Australia
inferredcites →https://doi.org/10.1071/ea98147openalex-snapshot
Yield responses of mulla mulla ( Ptilotus exaltatus Nees.) seedlings to additions of nitrogen, potassium and phosphorus fertiliser
inferredcites →https://doi.org/10.1071/fp06176openalex-snapshot
Root distributions of Australian herbaceous perennial legumes in response to phosphorus placement
inferredcites →https://doi.org/10.1071/s96060openalex-snapshot
Phosphorus requirements of Australian native plants
inferredcites →https://doi.org/10.1093/aob/mcp021openalex-snapshot
Putting the P in Ptilotus: a phosphorus-accumulating herb native to Australia
inferredcites →https://doi.org/10.1093/aob/mcq027openalex-snapshot
Comparative physiology of elemental distributions in plants
inferredcites →https://doi.org/10.1093/aob/mcs082openalex-snapshot
Complementarity in root architecture for nutrient uptake in ancient maize/bean and maize/bean/squash polycultures
inferredcites →https://doi.org/10.1093/jxb/44.3.587openalex-snapshot
Subcellular Distribution of Inorganic Phosphate, and Levels of Nucleoside Triphosphate, in Mature Maize Roots at Low External Phosphate Concentrations: Measurements with31P-NMR
inferredcites →https://doi.org/10.1093/jxb/erh111openalex-snapshot
Tissue and cellular phosphorus storage during development of phosphorus toxicity in Hakea prostrata (Proteaceae)
inferredcites →https://doi.org/10.1093/jxb/erj004openalex-snapshot
Systemic suppression of cluster-root formation and net P-uptake rates in Grevillea crithmifolia at elevated P supply: a proteacean with resistance for developing symptoms of ‘P toxicity’
inferredcites →https://doi.org/10.1098/rstb.2011.0243openalex-snapshot
New roots for agriculture: exploiting the root phenome
inferredcites →https://doi.org/10.1104/pp.111.174318openalex-snapshot
Phosphorus Nutrition of Proteaceae in Severely Phosphorus-Impoverished Soils: Are There Lessons To Be Learned for Future Crops?
inferredcites →https://doi.org/10.1104/pp.116.2.447openalex-snapshot
Phosphorus Uptake by Plants: From Soil to Cell
inferredcites →https://doi.org/10.1104/pp.122.3.835openalex-snapshot
Differential Ion Accumulation and Ion Fluxes in the Mesophyll and Epidermis of Barley
inferredcites →https://doi.org/10.1111/j.1365-3040.1993.tb00881.xopenalex-snapshot
Characteristics of inorganic nitrogen assimilation of plants in fire‐prone Mediterranean‐type vegetation
inferredcites →https://doi.org/10.1111/j.1365-3040.1993.tb00882.xopenalex-snapshot
15N natural abundance of plant and soil components of a Banksia woodland ecosystem in relation to nitrate utilization, life form, mycorrhizal status and N2‐fixing abilities of component species
inferredcites →https://doi.org/10.1111/j.1365-3040.2004.01204.xopenalex-snapshot
A root trait accounting for the extreme phosphorus sensitivity of Hakea prostrata (Proteaceae)
inferredcites →https://doi.org/10.1111/j.1365-3040.2008.01889.xopenalex-snapshot
Root of edaphically controlled Proteaceae turnover on the Agulhas Plain, South Africa: phosphate uptake regulation and growth
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01956.xopenalex-snapshot
Does phenotypic plasticity in carboxylate exudation differ among rare and widespread Banksia species (Proteaceae)?
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02573.xopenalex-snapshot
Anatomical traits associated with absorption and mycorrhizal colonization are linked to root branch order in twenty‐three Chinese temperate tree species
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04190.xopenalex-snapshot
Opportunities for improving phosphorus‐use efficiency in crop plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04285.xopenalex-snapshot
Proteaceae from severely phosphorus‐impoverished soils extensively replace phospholipids with galactolipids and sulfolipids during leaf development to achieve a high photosynthetic phosphorus‐use‐efficiency
inferredcites →https://doi.org/10.1111/pce.12210openalex-snapshot
Organ‐specific phosphorus‐allocation patterns and transcript profiles linked to phosphorus efficiency in two contrasting wheat genotypes
inferredcites →https://doi.org/10.1111/pce.12240openalex-snapshot
Low levels of ribosomal RNA partly account for the very high photosynthetic phosphorus‐use efficiency of P roteaceae species
inferredcites →https://doi.org/10.1139/b97-067openalex-snapshot
Morphological aspects of the shedding of surface layers from peanut roots
inferredcites →https://doi.org/10.2134/agronj1970.00021962006200020033xopenalex-snapshot
Phosphorus Concentrations in Wheat Leaves in Relation to Phosphorus Toxicity1
inferredcites →https://doi.org/10.2136/sssaj1979.03615995004300040009xopenalex-snapshot
Origin of the Effects of Citrate, Tartrate, and Acetate on Phosphate Sorption by Soils and Synthetic Gels
inferredcites →https://doi.org/10.2136/sssaj1982.03615995004600020027xopenalex-snapshot
Phosphorus Accumulation and Toxicity in Leaves in Relation to Zinc Supply
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.4793846openalex-extracted
The Growth and Physiological Response of Gleditsia Sinensis Lam. Seedlings with Different Phosphorus Efficiencies to Low Phosphorus Stress
inferred← citeshttps://doi.org/10.1007/s00344-022-10829-5openalex-snapshot
Low Phosphorus Tolerance in Cotton Genotypes is Regulated by Root Morphology and Physiology
inferred← citeshttps://doi.org/10.1007/s11104-015-2784-yopenalex-snapshot
Poor regulation of phosphorus uptake and rhizosphere carboxylates in three phosphorus-hyperaccumulating species of Ptilotus
inferred← citeshttps://doi.org/10.1007/s11104-017-3242-9openalex-snapshot
Growth, morphological and physiological responses of alfalfa (Medicago sativa) to phosphorus supply in two alkaline soils
inferred← citeshttps://doi.org/10.1016/j.apsoil.2016.12.011openalex-snapshot
Practicability of using Polygonum japonicum as a P accumulator for P phytoextraction from soil amended with swine manure
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2017.12.016openalex-snapshot
Subcellular distribution and chemical form of phosphorus involved in alleviating phosphorus toxicity of the phosphorus-accumulator Polygonum hydropiper
inferred← citeshttps://doi.org/10.1016/j.chemosphere.2020.128438openalex-snapshot
Accumulation of phosphorus and calcium in different cells protects the phosphorus-hyperaccumulator Ptilotus exaltatus from phosphorus toxicity in high-phosphorus soils
inferred← citeshttps://doi.org/10.1038/s41598-020-61147-3openalex-snapshot
Phosphorus (P) use efficiency in rice is linked to tissue-specific biomass and P allocation patterns
inferred← citeshttps://doi.org/10.1038/srep17835openalex-snapshot
P accumulation and physiological responses to different high P regimes in Polygonum hydropiper for understanding a P-phytoremediation strategy
inferred← citeshttps://doi.org/10.1071/bt19188openalex-snapshot
Mulling over the mulla mullas: revisiting phosphorus hyperaccumulation in the Australian plant genus Ptilotus (Amaranthaceae)
inferred← citeshttps://doi.org/10.1080/03650340.2018.1521957openalex-snapshot
Grain phosphorus and phytate contents of wheat genotypes released during last 6 decades and categorization of selected genotypes for phosphorus use efficiency
inferred← citeshttps://doi.org/10.1093/treephys/tpaf162openalex-snapshot
Decadal N and P addition reshapes multi-element allocation patterns and network interaction in subtropical plantation trees
inferred← citeshttps://doi.org/10.1111/pce.14895openalex-snapshot
Physiological and molecular responses in phosphorus‐hyperaccumulating Polygonum species to high phosphorus exposure
inferred← citeshttps://doi.org/10.1111/plb.13111openalex-snapshot
Effect of phosphorus efficiency on elemental stoichiometry of two shrubs
inferred← citeshttps://doi.org/10.1186/s12870-023-04100-6openalex-snapshot
Phosphorus and carbohydrate metabolism contributes to low phosphorus tolerance in cotton
inferred← citeshttps://doi.org/10.1371/journal.pone.0205471openalex-snapshot
Categorization of wheat genotypes for phosphorus efficiency
inferred← citeshttps://doi.org/10.3390/agronomy14102271openalex-snapshot
Unveiling the Effects of Phosphorus on the Mineral Nutrient Content and Quality of Alfalfa (Medicago sativa L.) in Acidic Soils
inferred← citeshttps://doi.org/10.3390/agronomy9110689openalex-snapshot
Genotypic Variation in Cotton Genotypes for Phosphorus-Use Efficiency
inferred← citeshttps://doi.org/10.3390/f15081343openalex-snapshot
The Growth and Physiological Responses of Gleditsia sinensis Lam. Seedlings with Different Phosphorus Efficiencies to Low Phosphorus Stress
inferred← citeshttps://doi.org/10.5772/intechopen.102595openalex-snapshot
Toward the Recent Advances in Nutrient Use Efficiency (NUE): Strategies to Improve Phosphorus Availability to Plants
inferred← citeshttps://doi.org/10.6084/m9.figshare.26568949openalex-snapshot
Additional file 1 of Phosphorus and carbohydrate metabolism contributes to low phosphorus tolerance in cotton
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