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Carbon–nitrogen relations of ectomycorrhizal mycelium across a natural nitrogen supply gradient in boreal forest
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Outgoing claims: the papers this work cites, builds on, or argues with.
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ConFlo III - an interface for high precision δ13C and δ15N analysis with an extended dynamic range
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Nitrogen in Terrestrial Ecosystems
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Alkylated ureas: mineralization and evaluation as N sources
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Production, standing biomass and natural abundance of 15 N and 13 C in ectomycorrhizal mycelia collected at different soil depths in two forest types
inferredcites →https://doi.org/10.1007/s00442-005-0253-7openalex-snapshot
Contrasting patterns of soil N-cycling in model ecosystems of Fennoscandian boreal forests
inferredcites →https://doi.org/10.1007/s00442-006-0562-5openalex-snapshot
Is microbial community composition in boreal forest soils determined by pH, C-to-N ratio, the trees, or all three?
inferredcites →https://doi.org/10.1007/s004420050163openalex-snapshot
Carbon isotope composition of boreal plants: functional grouping of life forms
inferredcites →https://doi.org/10.1007/s004420100680openalex-snapshot
Ecophysiology of 13C and 15N isotopic fractionation in forest fungi and the roots of the saprotrophic-mycorrhizal divide
inferredcites →https://doi.org/10.1007/s005720050261openalex-snapshot
The carbon origin of arbuscular mycorrhizal fungi estimated from δ 13 C values of individual spores
inferredcites →https://doi.org/10.1007/s10021-003-0191-3openalex-snapshot
Feldspar Tunneling by Fungi along Natural Productivity Gradients
inferredcites →https://doi.org/10.1007/s11104-013-1630-3openalex-snapshot
The production and turnover of extramatrical mycelium of ectomycorrhizal fungi in forest soils: role in carbon cycling
inferredcites →https://doi.org/10.1007/s11104-014-2091-zopenalex-snapshot
The return of an experimentally N-saturated boreal forest to an N-limited state: observations on the soil microbial community structure, biotic N retention capacity and gross N mineralisation
inferredcites →https://doi.org/10.1016/0045-2068(91)90048-topenalex-snapshot
Recent advances in the chemistry of an old enzyme, urease
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/b978-012088447-6/50004-0openalex-snapshot
Factors Determining the 13C Abundance of Soil-Respired CO2 in Boreal Forests
inferredcites →https://doi.org/10.1016/j.envpol.2018.11.074openalex-snapshot
Atmospheric nitrogen deposition impacts on the structure and function of forest mycorrhizal communities: A review
inferredcites →https://doi.org/10.1016/j.fgb.2008.01.002openalex-snapshot
Characterization and regulation of PiDur3, a permease involved in the acquisition of urea by the ectomycorrhizal fungus Paxillus involutus
inferredcites →https://doi.org/10.1016/j.foreco.2013.02.035openalex-snapshot
Relations among soil microbial community composition, nitrogen turnover, and tree growth in N-loaded and previously N-loaded boreal spruce forest
inferredcites →https://doi.org/10.1016/j.foreco.2017.04.045openalex-snapshot
Tamm Review: On the nature of the nitrogen limitation to plant growth in Fennoscandian boreal forests
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Strategies of carbon and nitrogen acquisition by saprotrophic and ectomycorrhizal fungi in Finnish boreal Picea abies-dominated forests
inferredcites →https://doi.org/10.1016/j.soilbio.2003.12.002openalex-snapshot
Nutrient limitations to soil microbial biomass and activity in loblolly pine forests
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Discrepancies between ergosterol and the phospholipid fatty acid 18:2ω6,9 as biomarkers for fungi in boreal forest soils
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Evaluation of methods to estimate production, biomass and turnover of ectomycorrhizal mycelium in forests soils – A review
inferredcites →https://doi.org/10.1016/j.soilbio.2019.107635openalex-snapshot
Does ectomycorrhiza have a universal key role in the formation of soil organic matter in boreal forests?
inferredcites →https://doi.org/10.1016/j.tree.2006.06.004openalex-snapshot
Towards a more plant physiological perspective on soil ecology
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The implications of exoenzyme activity on microbial carbon and nitrogen limitation in soil: a theoretical model
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Competition for nitrogen between plants and soil microorganisms
inferredcites →https://doi.org/10.1021/ic000933wopenalex-snapshot
Decomposition of Alkyl-Substituted Urea Molecules at a Hydroxide-Bridged Dinickel Center
inferredcites →https://doi.org/10.1023/a:1019698108838openalex-snapshot
Is growth of soil microorganisms in boreal forests limited by carbon or nitrogen availability?
inferredcites →https://doi.org/10.1038/31921openalex-snapshot
Boreal forest plants take up organic nitrogen
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Large-scale forest girdling shows that current photosynthesis drives soil respiration
inferredcites →https://doi.org/10.1038/ncomms9960openalex-snapshot
Social dynamics within decomposer communities lead to nitrogen retention and organic matter build-up in soils
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00199.xopenalex-snapshot
Estimation of the biomass and seasonal growth of external mycelium of ectomycorrhizal fungi in the field
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00788.xopenalex-snapshot
Natural 15N abundance in fruit bodies of ectomycorrhizal fungi from boreal forests
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00134.xopenalex-snapshot
Mycorrhizal vs saprotrophic status of fungi: the isotopic evidence
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00417.xopenalex-snapshot
Extramatrical ectomycorrhizal mycelium contributes one‐third of microbial biomass and produces, together with associated roots, half the dissolved organic carbon in a forest soil
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00470.xopenalex-snapshot
Direct nitrogen and phosphorus limitation of arbuscular mycorrhizal fungi: a model and field test
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00728.xopenalex-snapshot
Production of external mycelium by ectomycorrhizal fungi in a norway spruce forest was reduced in response to nitrogen fertilization
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00838.xopenalex-snapshot
Species level patterns in13C and15N abundance of ectomycorrhizal and saprotrophic fungal sporocarps
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00867.xopenalex-snapshot
Contrasting effects of nitrogen availability on plant carbon supply to mycorrhizal fungi and saprotrophs – a hypothesis based on field observations in boreal forest
inferredcites →https://doi.org/10.1073/pnas.96.15.8534openalex-snapshot
Natural 13 C abundance reveals trophic status of fungi and host-origin of carbon in mycorrhizal fungi in mixed forests
inferredcites →https://doi.org/10.1080/10242420210154openalex-snapshot
Review Properties and Applications of Urease
inferredcites →https://doi.org/10.1080/11956860.1997.11682382openalex-snapshot
Nitrogen limitation of the microbial biomass in an old-growth forest soil
inferredcites →https://doi.org/10.1093/femsre/fuy008openalex-snapshot
Bacterial–fungal interactions: ecology, mechanisms and challenges
inferredcites →https://doi.org/10.1093/treephys/21.2-3.71openalex-snapshot
Rates and quantities of carbon flux to ectomycorrhizal mycelium following 14C pulse labeling of Pinus sylvestris seedlings: effects of litter patches and interaction with a wood-decomposer fungus
inferredcites →https://doi.org/10.1099/00221287-139-5-957openalex-snapshot
Isolation and characterization of urease from Aspergillus niger
inferredcites →https://doi.org/10.1111/1365-2745.12917openalex-snapshot
Fungal community shifts underpin declining mycelial production and turnover across a Pinus sylvestris chronosequence
inferredcites →https://doi.org/10.1111/1462-2920.15132openalex-snapshot
Trait‐based approaches reveal fungal adaptations to nutrient‐limiting conditions
inferredcites →https://doi.org/10.1111/j.1365-2486.2007.01371.xopenalex-snapshot
Changes in nitrogen cycling and retention processes in soils under spruce forests along a nitrogen enrichment gradient in Germany
inferredcites →https://doi.org/10.1111/j.1462-2920.2008.01767.xopenalex-snapshot
Universal and species‐specific bacterial ‘fungiphiles’ in the mycospheres of different basidiomycetous fungi
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb04003.xopenalex-snapshot
Tansley Review No. 76 Helper bacteria: a new dimension to the mycorrhizal symbiosis
inferredcites →https://doi.org/10.1111/j.1469-8137.1995.tb01834.xopenalex-snapshot
The structure and function of the vegetative mycelium of ectomycorrhizal plants
inferredcites →https://doi.org/10.1111/j.1469-8137.1995.tb01835.xopenalex-snapshot
The structure and function of the vegetative mycelium of ectomycorrhizal plants
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01223.xopenalex-snapshot
Growth and biomass of mycorrhizal mycelia in coniferous forests along short natural nutrient gradients
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01718.xopenalex-snapshot
Species composition of an ectomycorrhizal fungal community along a local nutrient gradient in a boreal forest
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01742.xopenalex-snapshot
Measuring external mycelia production of ectomycorrhizal fungi in the field: the soil matrix matters
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01936.xopenalex-snapshot
Spatial separation of litter decomposition and mycorrhizal nitrogen uptake in a boreal forest
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02191.xopenalex-snapshot
The mycorrhiza helper bacteria revisited
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03204.xopenalex-snapshot
Spatial and temporal ecology of Scots pine ectomycorrhizas
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03274.xopenalex-snapshot
Quantification of effects of season and nitrogen supply on tree below‐ground carbon transfer to ectomycorrhizal fungi and other soil organisms in a boreal pine forest
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03485.xopenalex-snapshot
Recovery of ectomycorrhiza after ‘nitrogen saturation’ of a conifer forest
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04300.xopenalex-snapshot
Nitrogen isotopes link mycorrhizal fungi and plants to nitrogen dynamics
inferredcites →https://doi.org/10.1111/j.1574-6941.2009.00733.xopenalex-snapshot
Termination of belowground C allocation by trees alters soil fungal and bacterial communities in a boreal forest
inferredcites →https://doi.org/10.1111/j.1574-6941.2009.00807.xopenalex-snapshot
Mechanisms that promote bacterial fitness in fungal-affected soil microhabitats
inferredcites →https://doi.org/10.1111/nph.12139openalex-snapshot
Are ectomycorrhizal fungi alleviating or aggravating nitrogen limitation of tree growth in boreal forests?
inferredcites →https://doi.org/10.1111/nph.13201openalex-snapshot
Ectomycorrhizal fungi – potential organic matter decomposers, yet not saprotrophs
inferredcites →https://doi.org/10.1111/nph.15679openalex-snapshot
Exploring the role of ectomycorrhizal fungi in soil carbon dynamics
inferredcites →https://doi.org/10.1126/science.327543openalex-snapshot
Mechanism of Carbon Isotope Fractionation Associated with Lipid Synthesis
inferredcites →https://doi.org/10.1128/aem.00739-10openalex-snapshot
γ-Glutamylmethylamide Is an Essential Intermediate in the Metabolism of Methylamine by Methylocella silvestris
inferredcites →https://doi.org/10.1128/mmbr.53.1.85-108.1989openalex-snapshot
Microbial ureases: significance, regulation, and molecular characterization
inferredcites →https://doi.org/10.1890/0012-9658(1998)079[0119:scapif]2.0.co;2openalex-snapshot
SOIL CHEMISTRY AND PLANTS IN FENNOSCANDIAN BOREAL FOREST AS EXEMPLIFIED BY A LOCAL GRADIENT
inferredcites →https://doi.org/10.1890/0012-9658(2001)082[2245:fafoni]2.0.co;2openalex-snapshot
FLUXES AND FATES OF NITROGEN IN SOIL OF AN UNPOLLUTED OLD-GROWTH TEMPERATE FOREST, SOUTHERN CHILE
inferredcites →https://doi.org/10.1890/03-8002openalex-snapshot
NITROGEN MINERALIZATION: CHALLENGES OF A CHANGING PARADIGM
inferredcites →https://doi.org/10.1890/10-1011.1openalex-snapshot
Plants control the seasonal dynamics of microbial N cycling in a beech forest soil by belowground C allocation
inferredcites →https://doi.org/10.1890/15-1222.1openalex-snapshot
Greater carbon allocation to mycorrhizal fungi reduces tree nitrogen uptake in a boreal forest
inferredcites →https://doi.org/10.3389/fmicb.2017.01281openalex-snapshot
Carbon:Nitrogen:Phosphorus Stoichiometry in Fungi: A Meta-Analysis
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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How Does Forest Fertilization Influence Tree Productivity of Different Boreal Forests? An Analysis of Data from Commercial Forestry Across Sweden
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Identification of phosphorus sources using oxygen isotope signatures of the recalcitrant and residual phosphorus pools in soils and sediments
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Mycorrhizal symbiosis and the nitrogen nutrition of forest trees
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Ectomycorrhizal fungal diversity may be influenced by arbuscular mycorrhizal trees in mixed temperate forests
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Asymmetric responses of roots and hyphae to inorganic and organic nutrient additions: a global meta-analysis
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Mitigation potential of forests: challenges to carbon accrual in the ecosystem
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ACORN Review: NPK fertilizer use in loblolly pine plantations: Who are we really feeding?
inferred← citeshttps://doi.org/10.1016/j.jenvman.2024.124023openalex-snapshot
How does forest fertilization influence tree productivity of boreal forests? An analysis of data from commercial forestry across Sweden
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2025.180483openalex-snapshot
Nitrogen enhancement amplifies the precipitation-driven productivity allocation pattern in temperate and alpine grasslands
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Effects of long-term nitrogen addition on the shift of nitrogen cycle from open to closed along an age gradient of larch plantations in North China
inferred← citeshttps://doi.org/10.1016/j.soilbio.2025.109899openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.soilbio.2025.110070openalex-snapshot
Decoupled responses of mycorrhizal fungal communities and function to recurrent wildfire
inferred← citeshttps://doi.org/10.1021/acs.est.4c01662openalex-snapshot
Postfire Phosphorus Enrichment Mitigates Nitrogen Loss in Boreal Forests
inferred← citeshttps://doi.org/10.1073/pnas.2118852119openalex-snapshot
Metatranscriptomics captures dynamic shifts in mycorrhizal coordination in boreal forests
inferred← citeshttps://doi.org/10.1093/biosci/biaf018openalex-snapshot
Why not all productivity leads to carbon sequestration: the role of plant carbon surplus, allocation, and the Gadgil effect
inferred← citeshttps://doi.org/10.1093/jxb/erag010openalex-snapshot
Impact of nitrogen on ectomycorrhizal fungi: from resource exchange to forest carbon cycling
inferred← citeshttps://doi.org/10.1111/gcb.16768openalex-snapshot
Extraradical hyphae exhibit more plastic nutrient‐acquisition strategies than roots under nitrogen enrichment in ectomycorrhiza‐dominated forests
inferred← citeshttps://doi.org/10.1111/nph.19259openalex-snapshot
Modified source–sink dynamics govern resource exchange in ectomycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1111/nph.19509openalex-snapshot
Ectomycorrhizal fungi are more sensitive to high soil nitrogen levels in forests exposed to nitrogen deposition
inferred← citeshttps://doi.org/10.1111/nph.20205openalex-snapshot
Environmental dependency of ectomycorrhizal fungi as soil organic matter oxidizers
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Inorganic nitrogen and organic matter jointly regulate ectomycorrhizal fungi‐mediated iron acquisition
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Soil resource acquisition strategy modulates global plant nutrient and water economics
inferred← citeshttps://doi.org/10.1111/nph.70129openalex-snapshot
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Elevated CO2 mediates ectomycorrhizal fungi species‐specific decreases of native soil carbon and causes negative priming under low nutrients
inferred← citeshttps://doi.org/10.1111/nph.71165openalex-snapshot
Long‐term effects of clear‐cutting forestry on ectomycorrhizal fungi in boreal forest
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Comment on egusphere-2022-1351
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Earthworm-invaded boreal forest soils harbour distinct microbial communities
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