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Diversity of Mat-Forming Fungi in Relation to Soil Properties, Disturbance, and Forest Ecotype at Crater Lake National Park, Oregon, USA
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf00012043openalex-snapshot
Hyphal mats formed by two ectomycorrhizal fungi and their association with Douglas-fir seedlings: A case study
inferredcites →https://doi.org/10.1007/bf00015421openalex-snapshot
Spatial distribution of ectomycorrhizal mats in coniferous forests of the Pacific Northwest, USA
inferredcites →https://doi.org/10.1007/bf00205897openalex-snapshot
Water repellency, mat formation, and leaf-stimulated growth of some ectomycorrhizal fungi
inferredcites →https://doi.org/10.1007/bf00205898openalex-snapshot
Ectomycorrhizae of Sarcodon imbricatus on Norway spruce and their chlamydospores
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Ectomycorrhizae of Phellodon niger on Norway spruce and their chlamydospores
inferredcites →https://doi.org/10.1007/bf00207402openalex-snapshot
Extramatrical structures of hydrophobic and hydrophilic ectomycorrhizal fungi
inferredcites →https://doi.org/10.1007/bf00335767openalex-snapshot
Microbial characteristics of ectomycorrhizal mat communities in Oregon and California
inferredcites →https://doi.org/10.1007/bf00335839openalex-snapshot
Influence of ectomycorrhizal mat soils on lignin and cellulose degradation
inferredcites →https://doi.org/10.1007/s00442-003-1477-zopenalex-snapshot
Production, standing biomass and natural abundance of 15 N and 13 C in ectomycorrhizal mycelia collected at different soil depths in two forest types
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Slowed decomposition is biotically mediated in an ectomycorrhizal, tropical rain forest
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Morphological and molecular characterization of selected Ramaria mycorrhizae
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Genetic mosaics in the massive persisting rhizosphere colony “shiro” of the ectomycorrhizal basidiomycete Tricholoma matsutake
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Species richness and community composition of mat-forming ectomycorrhizal fungi in old- and second-growth Douglas-fir forests of the HJ Andrews Experimental Forest, Oregon, USA
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A manual of concise descriptions of North American ectomycorrhizae
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Exudation-reabsorption in a mycorrhizal fungus, the dynamic interface for interaction with soil and soil microorganisms
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Exploration types of ectomycorrhizae
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Stabilization and destabilization of soil organic matter—a new focus
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A conceptual model of organo-mineral interactions in soils: self-assembly of organic molecular fragments into zonal structures on mineral surfaces
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Lifespans of fungal rhizomorphs under nitrogen fertilization in a pinyon-juniper woodland
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Rock-eating mycorrhizas: their role in plant nutrition and biogeochemical cycles
inferredcites →https://doi.org/10.1007/s11104-009-0032-zopenalex-snapshot
Nitrogen isotopes in ectomycorrhizal sporocarps correspond to belowground exploration types
inferredcites →https://doi.org/10.1007/s11557-006-0505-xopenalex-snapshot
Fungal relationships and structural identity of their ectomycorrhizae
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Stable isotope geochemistry
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Patterns of basidiomycete nutrient accumulation in conifer and deciduous forest litter
inferredcites →https://doi.org/10.1016/0038-0717(79)90003-8openalex-snapshot
Calcium oxalate accumulation and soil weathering in mats of the hypogeous fungus Hysterangium crassum
inferredcites →https://doi.org/10.1016/0038-0717(92)90207-eopenalex-snapshot
Microbial biomass and nutrient concentrations in hyphal mats of the ectomycorrhizal fungus Hysterangium setchellii in a coniferous forest soil
inferredcites →https://doi.org/10.1016/0038-0717(93)90148-5openalex-snapshot
Nitrogen in ectomycorrhizal mat and non-mat soils of different-age douglas-fir forests
inferredcites →https://doi.org/10.1016/0038-0717(94)90282-8openalex-snapshot
Soil solution chemistry of ectomycorrhizal mats in forest soil
inferredcites →https://doi.org/10.1016/0167-8809(88)90063-1openalex-snapshot
Interactions between soil animals and ectomycorrhizal fungal mats
inferredcites →https://doi.org/10.1016/j.fbr.2010.03.002openalex-snapshot
The role of fungi in biogenic weathering in boreal forest soils
inferredcites →https://doi.org/10.1016/j.foreco.2005.08.007openalex-snapshot
Methods of microbial community profiling and their application to forest soils
inferredcites →https://doi.org/10.1016/j.foreco.2009.05.001openalex-snapshot
The foundational role of mycorrhizal networks in self-organization of interior Douglas-fir forests
inferredcites →https://doi.org/10.1016/j.foreco.2011.05.035openalex-snapshot
Growth and carbon sequestration by ectomycorrhizal fungi in intensively fertilized Norway spruce forests
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The fate of hydnoid fungi in The Netherlands and Northwestern Europe
inferredcites →https://doi.org/10.1016/j.funeco.2010.09.008openalex-snapshot
Conservation of ectomycorrhizal fungi: exploring the linkages between functional and taxonomic responses to anthropogenic N deposition
inferredcites →https://doi.org/10.1016/j.funeco.2010.11.001openalex-snapshot
Applying IUCN red-listing criteria for assessing and reporting on the conservation status of fungal species
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Biogeography of Hysterangiales (Phallomycetidae, Basidiomycota)
inferredcites →https://doi.org/10.1016/j.soilbio.2006.08.008openalex-snapshot
Hydraulic lift may buffer rhizosphere hyphae against the negative effects of severe soil drying in a California Oak savanna
inferredcites →https://doi.org/10.1016/j.soilbio.2007.08.005openalex-snapshot
From peds to paradoxes: Linkages between soil biota and their influences on ecological processes
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The role of ectomycorrhizal communities in forest ecosystem processes: New perspectives and emerging concepts
inferredcites →https://doi.org/10.1016/j.soilbio.2010.06.001openalex-snapshot
Ectomycorrhizal mats alter forest soil biogeochemistry
inferredcites →https://doi.org/10.1016/j.soilbio.2011.01.022openalex-snapshot
Distinctive fungal and bacterial communities are associated with mats formed by ectomycorrhizal fungi
inferredcites →https://doi.org/10.1016/s0007-1528(85)80076-6openalex-snapshot
Mushrooms and toadstools
inferredcites →https://doi.org/10.1016/s0007-1536(86)80160-7openalex-snapshot
An undescribed species of hypogeous Cortinarius associated with Eucalyptus in Western Australia
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Distribution of ectomycorrhizas in micro-habitats in mature and old-growth stands of Douglas-fir on southeastern Vancouver Island
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Advances in Understanding the Molecular Structure of Soil Organic Matter
inferredcites →https://doi.org/10.1016/s0953-7562(09)80928-3openalex-snapshot
Translocation of solutes in ectomycorrhizal and saprotrophic rhizomorphs
inferredcites →https://doi.org/10.1023/a:1006256231670openalex-snapshot
Mycorrhizal weathering: A true case of mineral plant nutrition?
inferredcites →https://doi.org/10.1038/35081058openalex-snapshot
Large-scale forest girdling shows that current photosynthesis drives soil respiration
inferredcites →https://doi.org/10.1038/41557openalex-snapshot
Net transfer of carbon between ectomycorrhizal tree species in the field
inferredcites →https://doi.org/10.1038/ismej.2010.19openalex-snapshot
Disruption of root carbon transport into forest humus stimulates fungal opportunists at the expense of mycorrhizal fungi
inferredcites →https://doi.org/10.1038/nature10386openalex-snapshot
Persistence of soil organic matter as an ecosystem property
inferredcites →https://doi.org/10.1038/scientificamerican0410-78openalex-snapshot
The Hidden Life of Truffles
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00030.xopenalex-snapshot
Nitrogen addition in a Norway spruce stand altered macromycete sporocarp production and below‐ground ectomycorrhizal species composition
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.1469-8137.2002.00367.xopenalex-snapshot
Ectomycorrhizal fungal taxa differing in response to nitrogen deposition also differ in pure culture organic nitrogen use and natural abundance of nitrogen isotopes
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.1469-8137.2003.00838.xopenalex-snapshot
Species level patterns in13C and15N abundance of ectomycorrhizal and saprotrophic fungal sporocarps
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Physical Properties of Woody Fuel Particles of Sierra Nevada Conifers
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Fatty Acid Esterase Production by Ectomycorrhizal Fungi
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Ectomycorrhizae of Hydnellum Peckii on Norway Spruce and their Chlamydospores
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Metal ion adsorption by pseudosclerotial plates of Phellinus weirii
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Saprotrophic Cord-Forming Fungi: Meeting the Challenge of Heterogeneous Environments
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Trees, Mycorrhiza and Minerals –Field Relevance ofin vitroExperiments
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Functional complementarity of Douglas‐fir ectomycorrhizas for extracellular enzyme activity after wildfire or clearcut logging
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MYCORRHIZAL ASSOCIATIONS IN SOME WOODLAND AND FOREST TREES AND SHRUBS IN TANZANIA
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ECTOMYCORRHIZAS OF TROPICAL ANGIOSPERMOUS TREES
inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00474.xopenalex-snapshot
15N natural abundance as a possible marker of the ectomycorrhizal habit of trees in mixed African woodlands
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb02976.xopenalex-snapshot
Decomposition of 14C‐labelled substrates by ectomycorrhizal fungi in association with Douglas fir
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01162.xopenalex-snapshot
Patterns of nitrogen and carbon stable isotope ratios in macrofungi, plants and soils in two old‐growth conifer forests
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01164.xopenalex-snapshot
Uptake of nitrogen and carbon from double‐labelled ( 15 N and 13 C) glycine by mycorrhizal pine seedlings
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01648.xopenalex-snapshot
Rapid nitrogen transfer from ectomycorrhizal pines to adjacent ectomycorrhizal and arbuscular mycorrhizal plants in a California oak woodland
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01669.xopenalex-snapshot
Fine‐scale distribution of pine ectomycorrhizas and their extramatrical mycelium
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.1469-8137.2007.01984.xopenalex-snapshot
Evidence that saprotrophic fungi mobilise carbon and mycorrhizal fungi mobilise nitrogen during litter decomposition
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02377.xopenalex-snapshot
Hydraulic redistribution of water from Pinus ponderosa trees to seedlings: evidence for an ectomycorrhizal pathway
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03003.xopenalex-snapshot
454 Pyrosequencing analyses of forest soils reveal an unexpectedly high fungal diversity
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.03069.xopenalex-snapshot
Architecture of the wood‐wide web: Rhizopogon spp. genets link multiple Douglas‐fir cohorts
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/10.1126/science.1206958openalex-snapshot
Archaeorhizomycetes: Unearthing an Ancient Class of Ubiquitous Soil Fungi
inferredcites →https://doi.org/10.1126/science.198.4323.1252openalex-snapshot
Calcium Oxalate: Occurrence in Soils and Effect on Nutrient and Geochemical Cycles
inferredcites →https://doi.org/10.1128/aem.00325-09openalex-snapshot
Calcium Oxalate Biomineralization by Piloderma fallax in Response to Various Levels of Calcium and Phosphorus
inferredcites →https://doi.org/10.1128/aem.69.1.327-333.2003openalex-snapshot
Molecular Identification of Ectomycorrhizal Mycelium in Soil Horizons
inferredcites →https://doi.org/10.1139/b00-085openalex-snapshot
Occurrence of Piloderma fallax in young, rotation-age, and old-growth stands of Douglas-fir (Pseudotsuga menziesii) in the Cascade Range of Oregon, U.S.A.
inferredcites →https://doi.org/10.1139/b04-060openalex-snapshot
Networks of power and influence: the role of mycorrhizal mycelium in controlling plant communities and agroecosystem functioning
inferredcites →https://doi.org/10.1139/b93-131openalex-snapshot
Dating the evolutionary radiations of the true fungi
inferredcites →https://doi.org/10.1139/x05-212openalex-snapshot
Seasonal fire effects on mixed-conifer forest structure and ponderosa pine resin properties
inferredcites →https://doi.org/10.1139/x07-014openalex-snapshot
Chemistry and ectomycorrhizal communities of coarse wood in young and old-growth forests in the Cascade Range of Oregon
inferredcites →https://doi.org/10.1139/x09-073openalex-snapshot
Relationships of current and past anthropogenic disturbance to mycorrhizal sporocarp fruiting patterns at Crater Lake National Park, Oregon
inferredcites →https://doi.org/10.1139/x89-087openalex-snapshot
Interaction effects of vegetation type and Pacific madrone soil inocula on survival, growth, and mycorrhiza formation of Douglas-fir
inferredcites →https://doi.org/10.1139/x90-030openalex-snapshot
Douglas-fir forest soils colonized by ectomycorrhizal mats. I. Seasonal variation in nitrogen chemistry and nitrogen cycle transformation rates
inferredcites →https://doi.org/10.1139/z85-162openalex-snapshot
Food habits of the northern flying squirrel (Glaucomys sabrinus) in Oregon
inferredcites →https://doi.org/10.1371/journal.pone.0000059openalex-snapshot
Taxonomic Reliability of DNA Sequences in Public Sequence Databases: A Fungal Perspective
inferredcites →https://doi.org/10.1385/0-89603-323-6:177openalex-snapshot
ITS-RFLP Matching for Identification of Fungi
inferredcites →https://doi.org/10.1525/9780520407114openalex-snapshot
Decomposition in Terrestrial Ecosystems
inferredcites →https://doi.org/10.1641/b571008openalex-snapshot
Soil Sensor Technology: Life within a Pixel
inferredcites →https://doi.org/10.2136/sssaj1972.03615995003600030035xopenalex-snapshot
Spodosol Development and Nutrient Distribution Under Hydnaceae Fungal Mats
inferredcites →https://doi.org/10.2307/1296341openalex-snapshot
Nutrient Cycling Pathways and Litter Fungi
inferredcites →https://doi.org/10.2307/1937216openalex-snapshot
Association of Vesicular‐Arbuscular Mycorrhizal Hyphae with Soil Organic Particles
inferredcites →https://doi.org/10.2307/2269397openalex-snapshot
Fire Severity and Tree Seedling Establishment in Abies Magnifica Forests, Southern Cascades, Oregon
inferredcites →https://doi.org/10.2307/3760788openalex-snapshot
Metal Ion Adsorption by Pseudosclerotial Plates of Phellinus weirii
inferredcites →https://doi.org/10.2478/som-1992-0001openalex-snapshot
Distribution and ecology of stipitate hydnaceous fungi in Norway, with special reference to the question of decline
inferredcites →https://doi.org/10.29203/ka.1974.85openalex-snapshot
Some type of mycorrhizae in the humus layer of conifer forests in Finland
inferredcites →https://doi.org/10.3852/10-125openalex-snapshot
Plugging into the network: belowground connections between germlings and extraradical mycelium of arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.4996/fireecology.0502030openalex-snapshot
Interactions among Prescribed Fire, Soil Attributes, and Mycorrhizal Community Structure at Crater Lake National Park, Oregon, USA
inferredcites →https://doi.org/10.5194/bg-9-2099-2012openalex-snapshot
Contributions of ectomycorrhizal fungal mats to forest soil respiration
inferredcites →https://doi.org/10.5962/p.415318openalex-snapshot
On Piloderma bicolor and the closely related P. byssinum, P. croceum and P. fallax
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.138320zenodo-depositor-declared
Fungal fairy rings: history, ecology, dynamics and engineering functions
inferred← citeshttps://doi.org/10.1007/s00572-025-01190-yopenalex-snapshot
Dynamics of pine ectomycorrhizae following root disturbance
inferred← citeshttps://doi.org/10.1007/s11104-026-08882-0openalex-snapshot
Truffles: diversification in niche construction in temperate ecosystems
inferred← citeshttps://doi.org/10.1007/s13199-016-0461-4openalex-snapshot
Hypogeous sequestrate fungi in South America – how well do we know them?
inferred← citeshttps://doi.org/10.1007/s13199-019-00617-3openalex-snapshot
Hysterangium atlanticum sp. nov., forms ectomycorrhizae with Coccoloba species (Polygonaceae) from the Atlantic rainforest of Northeastern Brazil
inferred← citeshttps://doi.org/10.1007/s13199-022-00869-6openalex-snapshot
Medium-distance soil foragers dominate the Pinus hartwegii ectomycorrhizal community at the 3900 m Neotropical treeline
inferred← citeshttps://doi.org/10.1016/j.foreco.2018.03.050openalex-snapshot
Recovery of ectomycorrhizal fungus communities fifteen years after fuels reduction treatments in ponderosa pine forests of the Blue Mountains, Oregon
inferred← citeshttps://doi.org/10.1016/j.soilbio.2023.109276openalex-snapshot
Niche construction by two ectomycorrhizal truffle species (Tuber aestivum and T. melanosporum)
inferred← citeshttps://doi.org/10.1111/oik.09567openalex-snapshot
Trees out‐forage understorey shrubs for nitrogen patches in a subarctic mountain birch forest
inferred← citeshttps://doi.org/10.1128/spectrum.04708-22openalex-snapshot
Fungal Hyphosphere Microbiomes Are Distinct from Surrounding Substrates and Show Consistent Association Patterns
inferred← citeshttps://doi.org/10.1186/s12866-026-04984-yopenalex-snapshot
The contribution of environmental DNA to exploring hypogeous fungal diversity and vulnerability
inferred← citeshttps://doi.org/10.1371/journal.pone.0168573openalex-snapshot
Distinctive Feature of Microbial Communities and Bacterial Functional Profiles in Tricholoma matsutake Dominant Soil
inferred← citeshttps://doi.org/10.3389/fmicb.2020.00347openalex-snapshot
Bacterial Community Selection of Russula griseocarnosa Mycosphere Soil
inferred← citeshttps://doi.org/10.3390/f13060824openalex-snapshot
First Report of Fungal Endophyte Communities and Non-Defensive Phytochemistry of Biocontrol-Inoculated Whitebark Pine Seedlings in a Restoration Planting
inferred← citeshttps://doi.org/10.3390/jof12010001openalex-snapshot
Phytomycobiomes and Ecosystem Services: Mechanisms, Evidence and Routes to Application
inferred← citeshttps://doi.org/10.3390/microorganisms12071329openalex-snapshot
Comparison of Bacterial Communities in Five Ectomycorrhizal Fungi Mycosphere Soil
inferred← citeshttps://doi.org/10.3390/microorganisms13030490openalex-snapshot
Soil Fungal Diversity and Community Structure of Russula griseocarnosa from Different Sites
inferred← citeshttps://doi.org/10.5194/bg-9-2099-2012openalex-snapshot
Contributions of ectomycorrhizal fungal mats to forest soil respiration
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