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Mycorrhizal networks: a review of their extent, function, and importance

https://doi.org/10.1139/b04-116
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TRANSPORT OF CARBON AMONG CONNECTED RAMETS OF EICHHORNIA CRASSIPES (PONTEDERIACEAE) AT NORMAL AND HIGH LEVELS OF CO 2
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Interspecific Nutrient Transfer in a Tallgrass Prairie Plant Community
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Towards Ecological Relevance — Progress and Pitfalls in the Path Towards an Understanding of Mycorrhizal Functions in Nature
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Arbuscular Mycorrhizal Fungi as a Determinant of Plant Diversity: in Search of Underlying Mechanisms and General Principles
inferredcites →https://doi.org/10.1007/978-3-540-38364-2_11openalex-snapshot
Dynamics within the Plant — Arbuscular Mycorrhizal Fungal Mutualism: Testing the Nature of Community Feedback
inferredcites →https://doi.org/10.1007/978-3-540-38364-2_17openalex-snapshot
Mycorrhizal Ecology: Synthesis and Perspectives
inferredcites →https://doi.org/10.1007/978-3-540-38364-2_2openalex-snapshot
Carbon and Nutrient Fluxes Within and Between Mycorrhizal Plants
inferredcites →https://doi.org/10.1007/978-3-540-38364-2_9openalex-snapshot
Diversity of Arbuscular Mycorrhizal Fungi and Ecosystem Functioning
inferredcites →https://doi.org/10.1007/978-3-662-10370-8_13openalex-snapshot
Altered Gene Expression During Ectomycorrhizal Development
inferredcites →https://doi.org/10.1007/978-94-009-6833-2_25openalex-snapshot
Sequences and interactions of mycorrhizal fungi on birch
inferredcites →https://doi.org/10.1007/978-94-009-6833-2_49openalex-snapshot
The structure and function of mycelial systems of ectomycorrhizal roots with special reference to their role in forming inter-plant connections and providing pathways for assimilate and water transport
inferredcites →https://doi.org/10.1007/bf00000102openalex-snapshot
The functioning of ectomycorrhizal fungi in the field: linkages in space and time
inferredcites →https://doi.org/10.1007/bf00011205openalex-snapshot
Specificity of interplant cycling of phosphorus: The role of mycorrhizas
inferredcites →https://doi.org/10.1007/bf00333217openalex-snapshot
Effect of arbuscular mycorrhiza on inter- and intraspecific competition of two grassland species
inferredcites →https://doi.org/10.1007/bf02182660openalex-snapshot
Sequences and interactions of mycorrhizal fungi on birch
inferredcites →https://doi.org/10.1007/bf02182684openalex-snapshot
The structure and function of mycelial systems of ectomycorrhizal roots with special reference to their role in forming inter-plant connections and providing pathways for assimilate and water transport
inferredcites →https://doi.org/10.1007/bf02912621openalex-snapshot
Positive interactions among plants
inferredcites →https://doi.org/10.1007/pl00013981openalex-snapshot
Spatial Distribution of the Subterranean Mycelia and Ectomycorrhizae of Suillus grevillei Genets
inferredcites →https://doi.org/10.1007/s003740050375openalex-snapshot
Density-dependent grazing on the extraradical hyphal network of the arbuscular mycorrhizal fungus, Glomus intraradices, by the collembolan, Folsomia candida
inferredcites →https://doi.org/10.1007/s003740050553openalex-snapshot
Colonization of nonmycorrhizal plants by mycorrhizal neighbours as influenced by the collembolan, Folsomia candida
inferredcites →https://doi.org/10.1007/s00442-002-0958-9openalex-snapshot
14C transfer between the spring ephemeral Erythronium americanum and sugar maple saplings via arbuscular mycorrhizal fungi in natural stands
inferredcites →https://doi.org/10.1007/s00572-001-0140-yopenalex-snapshot
Importance of the ectomycorrhizal network for seedling survival and ectomycorrhiza formation in rain forests of south Cameroon
inferredcites →https://doi.org/10.1007/s00572-005-0013-xopenalex-snapshot
Soil modification by different tree species influences the extent of seedling ectomycorrhizal infection
inferredcites →https://doi.org/10.1007/s00572-005-0018-5openalex-snapshot
Arbuscular mycorrhizal fungi in the tree seedlings of two Australian rain forests: occurrence, colonization, and relationships with plant performance
inferredcites →https://doi.org/10.1016/0014-5793(85)80331-8openalex-snapshot
15N‐NMR studies of nitrogen assimilation and amino acid biosynthesis in the ectomycorrhizal fungus Cenococcum graniforme
inferredcites →https://doi.org/10.1016/0038-0717(95)00117-4openalex-snapshot
Transfer of N and P from intact or decomposing roots of pea to barley interconnected by an arbuscular mycorrhizal fungus
inferredcites →https://doi.org/10.1016/0038-0717(95)00189-1openalex-snapshot
Carbon transfer between C3 and C4 plants linked by a common mycorrhizal network, quantified using stable carbon isotopes
inferredcites →https://doi.org/10.1016/0169-5347(94)90163-5openalex-snapshot
Species diversity in ecological communities
inferredcites →https://doi.org/10.1016/0929-1393(96)00092-3openalex-snapshot
Mycorrhizae, biocides, and biocontrol. 1. Herbicide-mycorrhiza interactions in soybean and cocklebur treated with bentazon
inferredcites →https://doi.org/10.1016/0929-1393(96)00093-5openalex-snapshot
Mycorrhizae, biocides, and biocontrol. 2. Mycorrhizal fungi enhance weed control and crop growth in a soybean-cocklebur association treated with the herbicide bentazon
inferredcites →https://doi.org/10.1016/j.pedobi.2005.05.007openalex-snapshot
Mycorrhizal diversity: Cause and effect?
inferredcites →https://doi.org/10.1016/s0038-0717(02)00036-6openalex-snapshot
The effect of earthworms and arbuscular mycorrhizal fungi on growth of and 32P transfer between Allium porrum plants
inferredcites →https://doi.org/10.1016/s0065-2504(08)60182-8openalex-snapshot
Mycorrhizal Links Between Plants: Their Functioning and Ecological Significance
inferredcites →https://doi.org/10.1016/s0167-8809(99)00087-0openalex-snapshot
The specificity of arbuscular mycorrhizal fungi in perennial ryegrass–white clover pasture
inferredcites →https://doi.org/10.1016/s0168-6445(98)00004-7openalex-snapshot
Physiology of organic nitrogen acquisition by ectomycorrhizal fungi and ectomycorrhizas
inferredcites →https://doi.org/10.1016/s0169-5347(98)01456-6openalex-snapshot
A moveable feast: the evolution of resource sharing in plant–fungus communities
inferredcites →https://doi.org/10.1016/s0169-5347(98)01540-7openalex-snapshot
Resource sharing in plant–fungus communities: did the carbon move for you?
inferredcites →https://doi.org/10.1016/s0169-5347(98)01563-8openalex-snapshot
Reply from D.A. Perry
inferredcites →https://doi.org/10.1016/s0929-1393(01)00165-2openalex-snapshot
Contrasting effects of microbial partners in the rhizosphere: interactions between Norway Spruce seedlings (Picea abies Karst.), mycorrhiza (Paxillus involutus (Batsch) Fr.) and naked amoebae (protozoa)
inferredcites →https://doi.org/10.1016/s0929-1393(97)00025-5openalex-snapshot
Mycorrhizal fungi influence competition in a wheat-ryegrass association treated with the herbicide diclofop
inferredcites →https://doi.org/10.1016/s0953-7562(08)61953-xopenalex-snapshot
Distribution and persistence of Amanita muscaria genotypes in Australian Pinus radiata plantations
inferredcites →https://doi.org/10.1016/s0953-7562(09)80496-6openalex-snapshot
Influence of intracellular phosphorus concentration on phosphate absorption by the ectomycorrhizal basidiomycete Pisolithus tinctorius
inferredcites →https://doi.org/10.1016/s0953-7562(09)81155-6openalex-snapshot
The role of the external mycelium of arbuscular mycorrhizal fungi in the carbon transfer process between plants
inferredcites →https://doi.org/10.1016/s1087-1845(03)00006-9openalex-snapshot
Carbohydrate and amino acid metabolism in Tuber borchii mycelium during glucose utilization: a 13C NMR study
inferredcites →https://doi.org/10.1017/s0953756202006263openalex-snapshot
A comparison of ectomycorrhiza identification based on morphotyping and PCR-RFLP analysis
inferredcites →https://doi.org/10.1023/a:1004205727882openalex-snapshot
Carbon allocation and carbon transfer between t Betula papyrifera and t Pseudotsuga menziesii seedlings using a 13C pulse-labeling method
inferredcites →https://doi.org/10.1023/a:1004257812555openalex-snapshot
Intraspecific transfer of carbon between plants linked by a common mycorrhizal network
inferredcites →https://doi.org/10.1023/a:1004312413711openalex-snapshot
Potential to improve transfer of N in intercropped systems by optimising host-endophyte combinations
inferredcites →https://doi.org/10.1034/j.1600-0706.2001.930301.xopenalex-snapshot
Context dependent effects of ectomycorrhizal species richness on tree seedling productivity
inferredcites →https://doi.org/10.1038/307053a0openalex-snapshot
Direct transfer of carbon between plants connected by vesicular–arbuscular mycorrhizal mycelium
inferredcites →https://doi.org/10.1038/31921openalex-snapshot
Boreal forest plants take up organic nitrogen
inferredcites →https://doi.org/10.1038/328420a0openalex-snapshot
Floristic diversity in a model system using experimental microcosms
inferredcites →https://doi.org/10.1038/35006630openalex-snapshot
Pervasive density-dependent recruitment enhances seedling diversity in a tropical forest
inferredcites →https://doi.org/10.1038/379063a0openalex-snapshot
Evolution of extreme specialization within a lineage of ectomycorrhizal epiparasites
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/nature01054openalex-snapshot
Epiparasitic plants specialized on arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00216.xopenalex-snapshot
The occurrence of anastomosis formation and nuclear exchange in intact arbuscular mycorrhizal networks
inferredcites →https://doi.org/10.1046/j.0028-646x.2001.00290.xopenalex-snapshot
Mycorrhizal synthesis between fungal strains of the Hymenoscyphus ericae aggregate and potential ectomycorrhizal and ericoid hosts
inferredcites →https://doi.org/10.1046/j.0962-1083.2001.01443.xopenalex-snapshot
Fine‐level mycorrhizal specificity in the Monotropoideae (Ericaceae): specificity for fungal species groups
inferredcites →https://doi.org/10.1046/j.1365-2435.1998.00206.xopenalex-snapshot
Carbon transfer between plants and its control in networks of arbuscular mycorrhizas
inferredcites →https://doi.org/10.1046/j.1365-2435.2002.00676.xopenalex-snapshot
Phosphorus uptake, not carbon transfer, explains arbuscular mycorrhizal enhancement of Centaurea maculosa in the presence of native grassland species
inferredcites →https://doi.org/10.1046/j.1365-2745.2001.00674.xopenalex-snapshot
Selectivity and functional diversity in arbuscular mycorrhizas of co‐occurring fungi and plants from a temperate deciduous woodland
inferredcites →https://doi.org/10.1046/j.1365-2745.2003.00829.xopenalex-snapshot
There is high potential for the formation of common mycorrhizal networks between understorey and canopy trees in a mixed evergreen forest
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00553.xopenalex-snapshot
Ectomycorrhizal fungal communities in late‐successional Swedish boreal forests, and their composition following wildfire
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00760.xopenalex-snapshot
Population, habitat and genetic correlates of mycorrhizal specialization in the ‘cheating’ orchids Corallorhiza maculata and C. mertensiana
inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01265.xopenalex-snapshot
Correspondence between genet diversity and spatial distribution of above‐ and below‐ground populations of the ectomycorrhizal fungus Hebeloma cylindrosporum
inferredcites →https://doi.org/10.1046/j.1365-294x.2003.01837.xopenalex-snapshot
Characterization of Pacific golden chanterelle (Cantharellus formosus) genet size using co‐dominant microsatellite markers
inferredcites →https://doi.org/10.1046/j.1461-0248.2002.00276.xopenalex-snapshot
A rodent plague on prairie diversity
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00731.xopenalex-snapshot
Effects of soil trenching on occurrence of ectomycorrhizas on Pseudotsuga menziesii seedlings grown in mature forests of Betula papyrifera and Pseudotsuga menziesii
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00834.xopenalex-snapshot
Reciprocal transfer of carbon isotopes between ectomycorrhizal Betula papyrifera and Pseudotsuga menziesii
inferredcites →https://doi.org/10.1046/j.1469-8137.1998.00122.xopenalex-snapshot
Genetic structure of a natural population of the ectomycorrhizal fungus Suillus pungens
inferredcites →https://doi.org/10.1046/j.1469-8137.1998.00185.xopenalex-snapshot
Multiple‐host fungi are the most frequent and abundant ectomycorrhizal types in a mixed stand of Douglas fir (Pseudotsuga menziesii) and bishop pine (Pinus muricata)
inferredcites →https://doi.org/10.1046/j.1469-8137.1998.00265.xopenalex-snapshot
Dark septate endophytes: a review of facultative biotrophic root‐colonizing fungi
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00383.xopenalex-snapshot
Continuity of ectomycorrhizal fungi in self‐regenerating boreal Pinus sylvestris forests studied by comparing mycobiont diversity on seedlings and mature trees
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00522.xopenalex-snapshot
Common anastomosis and internal transcribed spacer RFLP groupings in binucleate Rhizoctonia isolates representing root endophytes of Pinus sylvestris, Ceratorhiza spp. from orchid mycorrhizas and a phytopathogenic anastomosis group
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00592.xopenalex-snapshot
Symbiotic germination and development of myco‐heterotrophic plants in nature: transfer of carbon from ectomycorrhizal Salix repens and Betula pendula to the orchid Corallorhiza trifida through shared hyphal connections
inferredcites →https://doi.org/10.1046/j.1469-8137.2000.00698.xopenalex-snapshot
Does proximity to conspecific adults influence the establishment of ectomycorrhizal trees in rain forest?
inferredcites →https://doi.org/10.1046/j.1469-8137.2001.00010.xopenalex-snapshot
Can 14C‐labeled photosynthetic products move between Pinus densiflora seedlings linked by ectomycorrhizal mycelia?
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00468.xopenalex-snapshot
Survival of Suillus pungens and Amanita francheti ectomycorrhizal genets was rare or absent after a stand‐replacing wildfire
inferredcites →https://doi.org/10.1046/j.1469-8137.2002.00507.xopenalex-snapshot
Size, distribution, and persistence of genets in local populations of the late‐stage ectomycorrhizal basidiomycete, Russula brevipes
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00688.xopenalex-snapshot
Different arbuscular mycorrhizal fungi alter coexistence and resource distribution between co‐occurring plant
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00698.xopenalex-snapshot
Ectomycorrhizal fungal communities in young forest stands regenerating after clearcut logging
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00714.xopenalex-snapshot
Soil community feedback and the coexistence of competitors: conceptual frameworks and empirical tests
inferredcites →https://doi.org/10.1055/s-2005-872981openalex-snapshot
The Plant's Capacity in Regulating Resource Demand
inferredcites →https://doi.org/10.1073/pnas.94.9.4510openalex-snapshot
Independent, specialized invasions of ectomycorrhizal mutualism by two nonphotosynthetic orchids
inferredcites →https://doi.org/10.1093/icb/42.2.352openalex-snapshot
Host Specificity in Ectomycorrhizal Communities: What Do the Exceptions Tell Us?
inferredcites →https://doi.org/10.1093/jxb/50.330.9openalex-snapshot
The magnitude and control of carbon transfer between plants linked by a common mycorrhizal network
inferredcites →https://doi.org/10.1104/pp.010375openalex-snapshot
The Glyoxylate Cycle in an Arbuscular Mycorrhizal Fungus. Carbon Flux and Gene Expression
inferredcites →https://doi.org/10.1104/pp.101.3.865openalex-snapshot
Ammonia Assimilation in Zea mays L. Infected with a Vesicular-Arbuscular Mycorrhizal Fungus Glomus fasciculatum
inferredcites →https://doi.org/10.1104/pp.118.2.627openalex-snapshot
Carbohydrate and Amino Acid Metabolism in the Eucalyptus globulus-Pisolithus tinctorius Ectomycorrhiza during Glucose Utilization
inferredcites →https://doi.org/10.1104/pp.120.2.587openalex-snapshot
Carbon Uptake and the Metabolism and Transport of Lipids in an Arbuscular Mycorrhiza1
inferredcites →https://doi.org/10.1104/pp.86.3.935openalex-snapshot
Carbohydrate and Amino Acid Metabolism in the Ectomycorrhizal Ascomycete Sphaerosporella brunnea during Glucose Utilization
inferredcites →https://doi.org/10.1111/j.1399-3054.1960.tb08034.xopenalex-snapshot
Monotropa Hypopitys L. — an Epiparasite on Tree Roots
inferredcites →https://doi.org/10.1111/j.1469-8137.1965.tb05394.xopenalex-snapshot
CARBOHYDRATE PHYSIOLOGY OF MYCORRHIZAL ROOTS OF BEECH
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb02303.xopenalex-snapshot
ENHANCED CARBON TRANSFER BETWEEN ONIONS INFECTED WITH A VESICULAR‐ARBUSCULAR MYCORRHIZAL FUNGUS
inferredcites →https://doi.org/10.1111/j.1469-8137.1986.tb00603.xopenalex-snapshot
THE STRUCTURE AND FUNCTION OF THE VEGETATIVE MYCELIUM OF ECTOMYCORRHIZAL PLANTS
inferredcites →https://doi.org/10.1111/j.1469-8137.1986.tb00604.xopenalex-snapshot
THE STRUCTURE AND FUNCTION OF THE VEGETATIVE MYCELIUM OF ECTOMYCORRHIZAL PLANTS
inferredcites →https://doi.org/10.1111/j.1469-8137.1988.tb03704.xopenalex-snapshot
The structure and function of the vegetative mycelium of ectomycorrhizal plants IV. Qualitative analysis of carbohydrate contents of mycelium interconnecting host plants.
inferredcites →https://doi.org/10.1111/j.1469-8137.1989.tb00344.xopenalex-snapshot
Ectomycorrhizal mediation of competition between coniferous tree species
inferredcites →https://doi.org/10.1111/j.1469-8137.1989.tb02373.xopenalex-snapshot
Functional aspects of phosphorus uptake and carbon translocation in incompatible ectomycorrhizal associations between Pinus sylvestris and Suillus grevillei and Boletinus cauipes
inferredcites →https://doi.org/10.1111/j.1469-8137.1989.tb02394.xopenalex-snapshot
Uptake, translocation and assimilation of nitrogen from 15N‐labelled ammonium and nitrate sources by intact ectomycorrhizal systems of Fagus sylvatica infected with Paxillus involutus
inferredcites →https://doi.org/10.1111/j.1469-8137.1990.tb00370.xopenalex-snapshot
Structure and function of the interfaces in biotrophic symbioses as they relate to nutrient transport
inferredcites →https://doi.org/10.1111/j.1469-8137.1992.tb00072.xopenalex-snapshot
Transfer of symbiotically fixed nitrogen from berseem (Trifolium alexandrinumL.) to maize via vesicular—arbuscular mycorrhizal hyphae
inferredcites →https://doi.org/10.1111/j.1469-8137.1993.tb03812.xopenalex-snapshot
Nitrogen translocation between Alnus glutinosa (L.) Gaertn. seedlings inoculated with Frankia sp. and Pinus contorta Doug, ex Loud seedlings connected by a common ectomycorrhizal mycelium
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb02961.xopenalex-snapshot
Biology of the ectomycorrhizal genus, Rhizopogon
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb02962.xopenalex-snapshot
Biology of the ectomycorrhizal genus, Rhizopogon
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb04272.xopenalex-snapshot
The biology of myco‐heterotrophic (‘saprophytic’) plants
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.1469-8137.1996.tb04518.xopenalex-snapshot
Benomyl inhibits phosphorus transport but not fungal alkaline phosphatase activity in a Glomus–cucumber symbiosis
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01545.xopenalex-snapshot
Ectomycorrhizal networks and seedling establishment during early primary succession
inferredcites →https://doi.org/10.1111/j.1469-8137.2006.01612.xopenalex-snapshot
Common mycelial networks: life‐lines and radical addictions
inferredcites →https://doi.org/10.1139/b98-208openalex-snapshot
Ectomycorrhizal fungi associated with Arctostaphylos contribute to Pseudotsuga menziesii establishment
inferredcites →https://doi.org/10.1139/b99-109openalex-snapshot
A comparison of ectomycorrhiza communities from three conifer species planted on forest gap edges
inferredcites →https://doi.org/10.1139/b99-132openalex-snapshot
The effect of refuge trees on a paper birch ectomycorrhiza community
inferredcites →https://doi.org/10.1139/cjb-77-10-1523openalex-snapshot
The effect of refuge trees on a paper birch ectomycorrhiza community
inferredcites →https://doi.org/10.1139/cjfr-29-9-1322openalex-snapshot
Species richness of ectomycorrhizal fungi in cutblocks of different sizes in the Interior Cedar-Hemlock forests of northwestern British Columbia: sporocarps and ectomycorrhizae
inferredcites →https://doi.org/10.1139/cjfr-31-4-711openalex-snapshot
The potential for woody understory plants to provide refuge for ectomycorrhizal inoculum at an interior Douglas-fir forest after clear-cut logging
inferredcites →https://doi.org/10.1139/x02-141openalex-snapshot
Fluorescent pseudomonad population sizes baited from soils under pure birch, pure Douglas-fir, and mixed forest stands and their antagonism towardArmillaria ostoyaein vitro
inferredcites →https://doi.org/10.1139/x90-094openalex-snapshot
Growth and ectomycorrhiza formation of Douglas-fir seedlings grown in soils collected at different distances from pioneering hardwoods in southwest Oregon clear-cuts
inferredcites →https://doi.org/10.1139/x96-186openalex-snapshot
Shared compatibility of ectomycorrhizae on Pseudotsuga menziesii and Betula papyrifera seedlings grown in mixture in soils from southern British Columbia
inferredcites →https://doi.org/10.1139/x97-160openalex-snapshot
Ectomycorrhizal diversity on Betula papyrifera and Pseudotsuga menziesii seedlings grown in the greenhouse or outplanted in single-species and mixed plots in southern British Columbia
inferredcites →https://doi.org/10.1890/0012-9615(2002)072[0505:ioetom]2.0.co;2openalex-snapshot
INFLUENCES OF ESTABLISHED TREES ON MYCORRHIZAS, NUTRITION, AND GROWTH OF QUERCUS RUBRA SEEDLINGS
inferredcites →https://doi.org/10.1890/0012-9658(1998)079[2082:damfsa]2.0.co;2openalex-snapshot
DIFFERENT ARBUSCULAR MYCORRHIZAL FUNGAL SPECIES ARE POTENTIAL DETERMINANTS OF PLANT COMMUNITY STRUCTURE
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[1180:mieceo]2.0.co;2openalex-snapshot
MYCORRHIZAE INDIRECTLY ENHANCE COMPETITIVE EFFECTS OF AN INVASIVE FORB ON A NATIVE BUNCHGRASS
inferredcites →https://doi.org/10.1890/0012-9658(1999)080[1187:mipcsa]2.0.co;2openalex-snapshot
MYCORRHIZAE INFLUENCE PLANT COMMUNITY STRUCTURE AND DIVERSITY IN TALLGRASS PRAIRIE
inferredcites →https://doi.org/10.1890/0012-9658(2003)084[0129:sfateo]2.0.co;2openalex-snapshot
SOIL FUNGI AND THE EFFECTS OF AN INVASIVE FORB ON GRASSES: NEIGHBOR IDENTITY MATTERS
inferredcites →https://doi.org/10.1890/0012-9658(2003)084[0898:atomai]2.0.co;2openalex-snapshot
A TEST OF MUTUAL AID IN COMMON MYCORRHIZAL NETWORKS: ESTABLISHED VEGETATION NEGATES BENEFIT IN SEEDLINGS
inferredcites →https://doi.org/10.2135/cropsci1992.0011183x003200040032xopenalex-snapshot
Mycorrhizal Effects on Interspecific Plant Competition and Nitrogen Transfer in Legume‐Grass Mixtures
inferredcites →https://doi.org/10.2307/1934844openalex-snapshot
Translocation of C^(14)‐Labeled Compounds in Mycorrhizae and It Implications in Interplant Nutrient Cycling
inferredcites →https://doi.org/10.2307/2261676openalex-snapshot
Mycorrhizal Influence on Intra- and Interspecific Neighbour Interactions among Co-Occurring Prairie Grasses
inferredcites →https://doi.org/10.2307/2389658openalex-snapshot
Seedling Establishment Near Large Plants: Effects of Vesicular-Arbuscular Mycorrhizas on the Intensity of Plant Competition
inferredcites →https://doi.org/10.2307/2390019openalex-snapshot
Stimulative Effects of Arthropods on Endomycorrhizas of Sugar Maple in the Presence of Decaying Litter
inferredcites →https://doi.org/10.2307/2390139openalex-snapshot
Vesicular-Arbuscular Mycorrhizal Fungi: A Determinant of Plant Community Structure in Early Succession
inferredcites →https://doi.org/10.2307/2656829openalex-snapshot
High root concentration and uneven ectomycorrhizal diversity near Sarcodes sanguinea (Ericaceae): a cheater that stimulates its victims?
inferredcites →https://doi.org/10.2307/2960528openalex-snapshot
Incorporating the Soil Community into Plant Population Dynamics: The Utility of the Feedback Approach
inferredcites →https://doi.org/10.2307/3545818openalex-snapshot
Plant Coexistence in the Interactive Environment: Arbuscular Mycorrhiza Should Not Be out of Mind
inferredcites →https://doi.org/10.2307/3546272openalex-snapshot
Effect of Clipping, Benomyl, and Genet on 14 C Transfer between Mycorrhizal Plants
inferredcites →https://doi.org/10.2307/3546985openalex-snapshot
The Evolutionary Ecology of Mycorrhizal Networks
inferredcites →https://doi.org/10.5558/tfc68225-2openalex-snapshot
The value of managing for biodiversity

What points at this work

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

inferred← citeshttps://doi.org/10.53288/0404.1.00zenodo-depositor-declared
Solarities
inferred← citeshttps://doi.org/10.1002/9781118314364.ch4openalex-snapshot
Mycorrhizal Networks and Seedling Establishment in Douglas‐Fir Forests
inferred← citeshttps://doi.org/10.1002/9781118314364.ch5openalex-snapshot
Biology of Mycoheterotrophic and Mixotrophic Plants
inferred← citeshttps://doi.org/10.1002/9781119312994.apr0529openalex-snapshot
Mycorrhizal Associations and Phosphorus Acquisition: From Cells to Ecosystems
inferred← citeshttps://doi.org/10.1002/bies.201300092openalex-snapshot
Underground allies: How and why do mycelial networks help plants defend themselves?
inferred← citeshttps://doi.org/10.1002/ece3.24openalex-snapshot
Do mycorrhizal network benefits to survival and growth of interior Douglas‐fir seedlings increase with soil moisture stress?
inferred← citeshttps://doi.org/10.1002/imo2.46openalex-snapshot
Common mycorrhizal networks enhance defense responses against pathogens in neighboring plants
inferred← citeshttps://doi.org/10.1002/ppp3.10178openalex-snapshot
Can common mycorrhizal fungal networks be managed to enhance ecosystem functionality?
inferred← citeshttps://doi.org/10.1002/sae2.12018openalex-snapshot
Arbuscular mycorrhizal fungi prevent the negative effect of drought and modulate the growth‐defence trade‐off in tomato plants
inferred← citeshttps://doi.org/10.1002/uar2.20016openalex-snapshot
Designing multifunctional urban agroforestry with people in mind
inferred← citeshttps://doi.org/10.1007/124_2016_13openalex-snapshot
Beneficial Soil Microbiota as Mediators of the Plant Defensive Phenotype and Aboveground Plant-Herbivore Interactions
inferred← citeshttps://doi.org/10.1007/978-1-4020-8770-7_11openalex-snapshot
Ectomycorrhizae and Their Importance in Forest Ecosystems
inferred← citeshttps://doi.org/10.1007/978-1-4020-8770-7_12openalex-snapshot
Ectomycorrhizal Associations Function to Maintain Tropical Monodominance
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_8openalex-snapshot
The Physiological Ecology of Mycoheterotrophy
inferred← citeshttps://doi.org/10.1007/978-3-031-12994-0_20openalex-snapshot
The Current Scenario of the Distribution, Functionality, and Ecosystemic Role of the Arbuscular Mycorrhizal Symbiosis in Chile
inferred← citeshttps://doi.org/10.1007/978-3-031-12994-0_22openalex-snapshot
Gaps in South American Mycorrhizal Biodiversity and Ecosystem Function Research
inferred← citeshttps://doi.org/10.1007/978-3-032-08908-3_10openalex-snapshot
Altered Landscapes Versus Human Health: Processes
inferred← citeshttps://doi.org/10.1007/978-3-032-21303-7_42openalex-snapshot
Designing with Nature: Mycelium and Water for Urban Ecosystem Renewal in Łódź
inferred← citeshttps://doi.org/10.1007/978-3-319-57849-1_1openalex-snapshot
Carbon Fluxes in Mycorrhizal Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-59581-8_9openalex-snapshot
Following Nature’s Lead
inferred← citeshttps://doi.org/10.1007/978-3-319-75596-0_10openalex-snapshot
Mycorrhizal Networks Facilitate Tree Communication, Learning, and Memory
inferred← citeshttps://doi.org/10.1007/978-3-319-76956-1_16openalex-snapshot
Environmental Ethics of Forest Health: Alternative Stories of Asian Longhorn Beetle Management in the UK
inferred← citeshttps://doi.org/10.1007/978-3-540-70618-2_13openalex-snapshot
Network Organisation of Mycelial Fungi
inferred← citeshttps://doi.org/10.1007/978-3-540-78826-3_28openalex-snapshot
Community Developmental Patterns and Ecological Functions of Ectomycorrhizal Fungi: Implications from Primary Succession
inferred← citeshttps://doi.org/10.1007/978-3-540-87978-7_13openalex-snapshot
Response Diversity of Ectomycorrhizas in Forest Succession Following Disturbance
inferred← citeshttps://doi.org/10.1007/978-3-642-01284-6_4openalex-snapshot
Adaptive Biological Networks
inferred← citeshttps://doi.org/10.1007/978-3-642-05076-3_9openalex-snapshot
Mycorrhizal Associations in Agroforestry Systems
inferred← citeshttps://doi.org/10.1007/978-3-642-13145-5_13openalex-snapshot
Space as a Resource
inferred← citeshttps://doi.org/10.1007/978-3-642-15196-5_12openalex-snapshot
A Conceptual Framework for Up-Scaling Ecological Processes and Application to Ectomycorrhizal Fungi
inferred← citeshttps://doi.org/10.1007/978-3-642-23327-2_10openalex-snapshot
Role of Mycorrhiza in Re-forestation at Heavy Metal-Contaminated Sites
inferred← citeshttps://doi.org/10.1007/978-3-642-27515-9_5openalex-snapshot
The Impact of Mycorrhizosphere Bacterial Communities on Soil Biofunctioning in Tropical and Mediterranean Forest Ecosystems
inferred← citeshttps://doi.org/10.1007/978-3-642-33802-1_17openalex-snapshot
Plant Nitrogen Use Efficiency May Be Improved Through Symbiosis with Piriformospora indica
inferred← citeshttps://doi.org/10.1007/978-3-642-33811-3_13openalex-snapshot
Upscaling the Biogeochemical Role of Arbuscular Mycorrhizal Fungi in Metal Mobility
inferred← citeshttps://doi.org/10.1007/978-3-642-38797-5_10openalex-snapshot
Beyond Mutualism: Complex Mycorrhizal Interactions
inferred← citeshttps://doi.org/10.1007/978-81-322-2056-5_1openalex-snapshot
Insight into the Role of Arbuscular Mycorrhizal Fungi in Sustainable Agriculture
inferred← citeshttps://doi.org/10.1007/978-81-322-2169-2_9openalex-snapshot
Role of Microorganisms in Plant Nutrition and Health
inferred← citeshttps://doi.org/10.1007/978-90-481-9489-6_10openalex-snapshot
Biotic Environment of the Arbuscular Mycorrhizal Fungi in Soil
inferred← citeshttps://doi.org/10.1007/978-94-007-6167-4_603-1openalex-snapshot
Fungi Ethics
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9openalex-snapshot
Mycorrhizal Networks
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_1openalex-snapshot
Mycorrhiza Specificity: Its Role in the Development and Function of Common Mycelial Networks
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_5openalex-snapshot
Resource Transfer Between Plants Through Ectomycorrhizal Fungal Networks
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_6openalex-snapshot
The Role of Ectomycorrhizal Networks in Seedling Establishment and Primary Succession
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_7openalex-snapshot
Facilitation and Antagonism in Mycorrhizal Networks
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_9openalex-snapshot
Experimentally Testing Effects of Mycorrhizal Networks on Plant-Plant Interactions and Distinguishing Among Mechanisms
inferred← citeshttps://doi.org/10.1007/978-94-024-1179-9_603openalex-snapshot
Fungi Ethics
inferred← citeshttps://doi.org/10.1007/978-981-99-8220-2openalex-snapshot
Arbuscular Mycorrhizal Fungi and Higher Plants
inferred← citeshttps://doi.org/10.1007/978-981-99-8220-2_13openalex-snapshot
Arbuscular Mycorrhizal Fungi Under Intercrop, Regenerative, and Conventional Agriculture Systems
inferred← citeshttps://doi.org/10.1007/s00374-011-0576-yopenalex-snapshot
Phosphorus threshold for arbuscular mycorrhizal colonization of crops and tree seedlings
inferred← citeshttps://doi.org/10.1007/s00374-012-0682-5openalex-snapshot
Cumulative effects of tree-based intercropping on arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1007/s00374-012-0689-yopenalex-snapshot
Role of arbuscular mycorrhizal network in carbon and phosphorus transfer between plants
inferred← citeshttps://doi.org/10.1007/s00442-006-0581-2openalex-snapshot
Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae
inferred← citeshttps://doi.org/10.1007/s00442-007-0852-6openalex-snapshot
Tree proximity, soil pathways and common mycorrhizal networks: their influence on the utilization of redistributed water by understory seedlings
inferred← citeshttps://doi.org/10.1007/s00442-008-0962-9openalex-snapshot
Site-dependent N uptake from N-form mixtures by arctic plants, soil microbes and ectomycorrhizal fungi
inferred← citeshttps://doi.org/10.1007/s00442-008-1136-5openalex-snapshot
Mycorrhizal networks and distance from mature trees alter patterns of competition and facilitation in dry Douglas-fir forests
inferred← citeshttps://doi.org/10.1007/s00442-011-1928-xopenalex-snapshot
Root fungal symbionts interact with mammalian herbivory, soil nutrient availability and specific habitat conditions
inferred← citeshttps://doi.org/10.1007/s00442-015-3534-9openalex-snapshot
Density-dependent dynamics of a dominant rain forest tree change with juvenile stage and time of masting
inferred← citeshttps://doi.org/10.1007/s00442-018-4241-0openalex-snapshot
Additive or synergistic? Early ectomycorrhizal fungal community response to mixed tree plantings in boreal forest reclamation
inferred← citeshttps://doi.org/10.1007/s00442-021-04868-0openalex-snapshot
Aboveground herbivores drive stronger plant species-specific feedback than belowground fungi to regulate tree community assembly
inferred← citeshttps://doi.org/10.1007/s00468-007-0164-9openalex-snapshot
The ectomycorrhizal community structure in high mountain Norway spruce stands
inferred← citeshttps://doi.org/10.1007/s00572-005-0013-xopenalex-snapshot
Soil modification by different tree species influences the extent of seedling ectomycorrhizal infection
inferred← citeshttps://doi.org/10.1007/s00572-005-0018-5openalex-snapshot
Arbuscular mycorrhizal fungi in the tree seedlings of two Australian rain forests: occurrence, colonization, and relationships with plant performance
inferred← citeshttps://doi.org/10.1007/s00572-006-0083-4openalex-snapshot
Methods to control ectomycorrhizal colonization: effectiveness of chemical and physical barriers
inferred← citeshttps://doi.org/10.1007/s00572-007-0123-8openalex-snapshot
Spatial patterns of ectomycorrhizal fungal inoculum in arbuscular mycorrhizal barrens communities: implications for controlling invasion by Pinus virginiana
inferred← citeshttps://doi.org/10.1007/s00572-007-0150-5openalex-snapshot
Nitrogen sink strength of ectomycorrhizal morphotypes of Quercus douglasii, Q. garryana, and Q. agrifolia seedlings grown in a northern California oak woodland
inferred← citeshttps://doi.org/10.1007/s00572-008-0185-2openalex-snapshot
Neighboring trees affect ectomycorrhizal fungal community composition in a woodland-forest ecotone
inferred← citeshttps://doi.org/10.1007/s00572-009-0228-3openalex-snapshot
Field persistence of the edible ectomycorrhizal fungus Lactarius deliciosus: effects of inoculation strain, initial colonization level, and site characteristics
inferred← citeshttps://doi.org/10.1007/s00572-009-0261-2openalex-snapshot
Land use practices and ectomycorrhizal fungal communities from oak woodlands dominated by Quercus suber L. considering drought scenarios
inferred← citeshttps://doi.org/10.1007/s00572-010-0336-0openalex-snapshot
Arbuscular mycorrhizal propagules in soils from a tropical forest and an abandoned cornfield in Quintana Roo, Mexico: visual comparison of most-probable-number estimates
inferred← citeshttps://doi.org/10.1007/s00572-010-0340-4openalex-snapshot
Arbuscular mycorrhizal inoculum potential: a mechanism promoting positive diversity–invasibility relationships in mountain beech forests in New Zealand?
inferred← citeshttps://doi.org/10.1007/s00572-013-0539-2openalex-snapshot
Comparison of root-associated communities of native and non-native ectomycorrhizal hosts in an urban landscape
inferred← citeshttps://doi.org/10.1007/s00572-014-0597-0openalex-snapshot
Sharing rotting wood in the shade: ectomycorrhizal communities of co-occurringbirch and hemlock seedlings
inferred← citeshttps://doi.org/10.1007/s00572-015-0668-xopenalex-snapshot
Ectomycorrhizal communities of ponderosa pine and lodgepole pine in the south-central Oregon pumice zone
inferred← citeshttps://doi.org/10.1007/s00572-015-0671-2openalex-snapshot
Different levels of hyphal self-incompatibility modulate interconnectedness of mycorrhizal networks in three arbuscular mycorrhizal fungi within the Glomeraceae
inferred← citeshttps://doi.org/10.1007/s00572-016-0733-0openalex-snapshot
Mycorrhizal compatibility and symbiotic seed germination of orchids from the Coastal Range and Andes in south central Chile
inferred← citeshttps://doi.org/10.1007/s00572-016-0749-5openalex-snapshot
Nutrient enrichment effects on mycorrhizal fungi in an Andean tropical montane Forest
inferred← citeshttps://doi.org/10.1007/s00572-017-0776-xopenalex-snapshot
An empirical investigation of the possibility of adaptability of arbuscular mycorrhizal fungi to new hosts
inferred← citeshttps://doi.org/10.1007/s00572-017-0801-0openalex-snapshot
Arbuscular common mycorrhizal networks mediate intra- and interspecific interactions of two prairie grasses
inferred← citeshttps://doi.org/10.1007/s00572-017-0817-5openalex-snapshot
Ectomycorrhizal fungal communities in alpine relict forests of Pinus pumila on Mt. Norikura, Japan
inferred← citeshttps://doi.org/10.1007/s00572-020-00940-4openalex-snapshot
The effects of ectomycorrhizal fungal networks on seedling establishment are contingent on species and severity of overstorey mortality
inferred← citeshttps://doi.org/10.1007/s00572-020-00959-7openalex-snapshot
Rapid nitrogen loss from ectomycorrhizal pine germinants signaled by their fungal symbiont
inferred← citeshttps://doi.org/10.1007/s00572-021-01053-2openalex-snapshot
A historical perspective on mycorrhizal mutualism emphasizing arbuscular mycorrhizas and their emerging challenges
inferred← citeshttps://doi.org/10.1007/s00572-023-01112-wopenalex-snapshot
Primary succession of ectomycorrhizal fungi associated with Alnus sieboldiana on Izu-Oshima Island, Japan
inferred← citeshttps://doi.org/10.1007/s10021-011-9502-2openalex-snapshot
Ectomycorrhizal Networks of Pseudotsuga menziesii var. glauca Trees Facilitate Establishment of Conspecific Seedlings Under Drought
inferred← citeshttps://doi.org/10.1007/s10342-017-1029-4openalex-snapshot
Influence of soil properties and burial depth on Persian oak (Quercus brantii Lindl.) establishment in different microhabitats resulting from traditional forest practices
inferred← citeshttps://doi.org/10.1007/s10530-022-02988-zopenalex-snapshot
Interactions between soil microbes and native species drive a diversity-invasibility relationship
inferred← citeshttps://doi.org/10.1007/s10531-022-02436-3openalex-snapshot
The relationship between green roofs and urban biodiversity: a systematic review
inferred← citeshttps://doi.org/10.1007/s10705-023-10334-5openalex-snapshot
Uptake of biocrust nitrogen by tree crops in a sandy soil agroecosystem
inferred← citeshttps://doi.org/10.1007/s11104-005-3081-yopenalex-snapshot
Nitrogen Transfer Between Plants: A 15N Natural Abundance Study with Crop and Weed Species
inferred← citeshttps://doi.org/10.1007/s11104-006-9091-6openalex-snapshot
The invasive plant species Centaurea maculosa alters arbuscular mycorrhizal fungal communities in the field
inferred← citeshttps://doi.org/10.1007/s11104-008-9603-7openalex-snapshot
Minimum pulses of stable and radioactive carbon isotopes to detect belowground carbon transfer between plants
inferred← citeshttps://doi.org/10.1007/s11104-009-9991-3openalex-snapshot
The rhizosphere zoo: An overview of plant-associated communities of microorganisms, including phages, bacteria, archaea, and fungi, and of some of their structuring factors
inferred← citeshttps://doi.org/10.1007/s11104-010-0621-xopenalex-snapshot
Soil microbial communities from an elevational cline differ in their effect on conifer seedling growth
inferred← citeshttps://doi.org/10.1007/s11104-019-04398-yopenalex-snapshot
Spatial patterns in soil organic matter dynamics are shaped by mycorrhizosphere interactions in a treeline forest
inferred← citeshttps://doi.org/10.1007/s11104-022-05315-6openalex-snapshot
The policy and ecology of forest-based climate mitigation: challenges, needs, and opportunities
inferred← citeshttps://doi.org/10.1007/s11104-023-06197-yopenalex-snapshot
Native mycorrhizal communities in maize roots as affected by plant genotype, starter fertilization and a seed-applied biostimulant
inferred← citeshttps://doi.org/10.1007/s11104-024-06751-2openalex-snapshot
Arbuscular and ectomycorrhizal tree seedling growth is inhibited by competition from neighboring roots and associated fungal hyphae
inferred← citeshttps://doi.org/10.1007/s11258-020-01031-2openalex-snapshot
Revegetation technique changes root mycorrhizal colonisation and root fungal communities: the advantage of direct seeding over transplanting tube-stock in riparian ecosystems
inferred← citeshttps://doi.org/10.1007/s11356-019-04385-xopenalex-snapshot
Nitrogen transfer from one plant to another depends on plant biomass production between conspecific and heterospecific species via a common arbuscular mycorrhizal network
inferred← citeshttps://doi.org/10.1007/s12080-015-0251-2openalex-snapshot
Interactions among mutualism, competition, and predation foster species coexistence in diverse communities
inferred← citeshttps://doi.org/10.1007/s12223-014-0374-7openalex-snapshot
Site properties have a stronger influence than fire severity on ectomycorrhizal fungi and associated N-cycling bacteria in regenerating post-beetle-killed lodgepole pine forests
inferred← citeshttps://doi.org/10.1007/s12229-017-9196-zopenalex-snapshot
Studies on Ectomycorrhiza: An Appraisal
inferred← citeshttps://doi.org/10.1007/s13199-011-0107-5openalex-snapshot
Arbuscular mycorrhizal fungal phylogeny-related interactions with a non-host
inferred← citeshttps://doi.org/10.1007/s13199-023-00948-2openalex-snapshot
Effect of agricultural management practices on diversity, abundance, and infectivity of arbuscular mycorrhizal fungi: a review
inferred← citeshttps://doi.org/10.1007/s13593-020-00647-yopenalex-snapshot
Forty years of study on interactions between walnut tree and arbuscular mycorrhizal fungi. A review
inferred← citeshttps://doi.org/10.1007/s40502-019-00491-7openalex-snapshot
Interplant communication via hyphal networks
inferred← citeshttps://doi.org/10.1007/s42832-021-0107-1openalex-snapshot
The roles and performance of arbuscular mycorrhizal fungi in intercropping systems
inferred← citeshttps://doi.org/10.1016/b978-0-12-409548-9.09135-1openalex-snapshot
Plant Ecology
inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00011-5openalex-snapshot
Integrating Ectomycorrhizas Into Sustainable Management of Temperate Forests
inferred← citeshttps://doi.org/10.1016/b978-0-12-804312-7.00018-8openalex-snapshot
Mycorrhizal Networks and Forest Resilience to Drought
inferred← citeshttps://doi.org/10.1016/b978-0-12-822974-3.00251-2openalex-snapshot
Fungi including mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/b978-0-443-18870-1.00013-5openalex-snapshot
Ectomycorrhizal fungi as biofertilizers in forestry restoration in Africa
inferred← citeshttps://doi.org/10.1016/b978-0-443-21903-0.00012-6openalex-snapshot
Arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/b978-0-443-21964-1.00021-5openalex-snapshot
Plant Ecology
inferred← citeshttps://doi.org/10.1016/b978-0-443-24863-4.00015-7openalex-snapshot
Mycorrhizae and soil pathogens in tropical regions
inferred← citeshttps://doi.org/10.1016/b978-0-443-45130-0.00032-1openalex-snapshot
Arbuscular mycorrhizal fungi as key players in soil health: Eco-physiological approaches toward sustainable agriculture
inferred← citeshttps://doi.org/10.1016/b978-0-444-63998-1.00016-1openalex-snapshot
Assessing soil biological health in forest soils
inferred← citeshttps://doi.org/10.1016/b978-0-444-64325-4.00017-1openalex-snapshot
Plant growth promoting myco-stimulation for sustainable agriculture production under abiotic stress
inferred← citeshttps://doi.org/10.1016/b978-012370526-6.50020-9openalex-snapshot
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From science to stewardship: Harnessing forest ecology in the service of society
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inferred← citeshttps://doi.org/10.1016/j.foreco.2018.01.037openalex-snapshot
Community-based biotic effects as determinants of tree resistance to pests and pathogens
inferred← citeshttps://doi.org/10.1016/j.foreco.2018.04.015openalex-snapshot
Effects of plant neighborhood on arbuscular mycorrhizal fungal attributes in afforested zones
inferred← citeshttps://doi.org/10.1016/j.foreco.2020.118388openalex-snapshot
Ecological drivers of root grafting in balsam fir natural stands
inferred← citeshttps://doi.org/10.1016/j.foreco.2021.119192openalex-snapshot
Nutrient deficiency enhances the rate of short-term belowground transfer of nitrogen from Acacia mangium to Eucalyptus trees in mixed-species plantations
inferred← citeshttps://doi.org/10.1016/j.foreco.2021.119375openalex-snapshot
Can understory functional traits predict post-harvest forest productivity in boreal ecosystems?
inferred← citeshttps://doi.org/10.1016/j.foreco.2022.120735openalex-snapshot
Context matters: Natural tree mortality can lead to neighbor growth release or suppression
inferred← citeshttps://doi.org/10.1016/j.foreco.2024.121853openalex-snapshot
Bottom-up population regulation of Orthotomicus erosus on irrigated and fertilized Pinus eldarica: A comprehensive field study
inferred← citeshttps://doi.org/10.1016/j.foreco.2026.123589openalex-snapshot
Deriving and assessing forest gap thresholds to prevent shallow landslides in Swiss mountain forests
inferred← citeshttps://doi.org/10.1016/j.funeco.2008.11.003openalex-snapshot
Role of mycorrhizal networks and tree proximity in ectomycorrhizal colonization of planted seedlings
inferred← citeshttps://doi.org/10.1016/j.funeco.2009.10.005openalex-snapshot
Co-existing ericaceous plant species in a subarctic mire community share fungal root endophytes
inferred← citeshttps://doi.org/10.1016/j.funeco.2016.08.007openalex-snapshot
Influences of host plant identity and disturbance on spatial structure and community composition of ectomycorrhizal fungi in a northern Mississippi uplands ecosystem
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.05.003openalex-snapshot
Processes underlying the effect of mycorrhizal symbiosis on plant-plant interactions
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2015.10.016openalex-snapshot
Nurse effect and soil microorganisms are key to improve the establishment of native plants in a semiarid community
inferred← citeshttps://doi.org/10.1016/j.landurbplan.2010.04.005openalex-snapshot
Fungi and the urban environment: A review
inferred← citeshttps://doi.org/10.1016/j.pedobi.2005.05.007openalex-snapshot
Mycorrhizal diversity: Cause and effect?
inferred← citeshttps://doi.org/10.1016/j.pedobi.2011.03.003openalex-snapshot
Dual plant host effects on two arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/j.pld.2021.06.005openalex-snapshot
Non-host plants: Are they mycorrhizal networks players?
inferred← citeshttps://doi.org/10.1016/j.ppees.2016.01.004openalex-snapshot
Soil fungi promote nitrogen transfer among plants involved in long-lasting facilitative interactions
inferred← citeshttps://doi.org/10.1016/j.ppees.2016.01.005openalex-snapshot
Disrupting ectomycorrhizal symbiosis: Indirect effects of an annual invasive plant on growth and survival of beech (Fagus sylvatica) saplings
inferred← citeshttps://doi.org/10.1016/j.revpalbo.2015.01.005openalex-snapshot
Arbuscular mycorrhizal fungi in a voltzialean conifer from the Triassic of Antarctica
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101221openalex-snapshot
Plant-to-plant carbon transfer responds to the density of the arbuscular mycorrhizal mycelial network
inferred← citeshttps://doi.org/10.1016/j.soilbio.2009.12.006openalex-snapshot
The role of ectomycorrhizal communities in forest ecosystem processes: New perspectives and emerging concepts
inferred← citeshttps://doi.org/10.1016/j.soilbio.2011.06.020openalex-snapshot
Nurse shrubs increased the early growth of Cupressus seedlings by enhancing belowground mutualism and soil microbial activity
inferred← citeshttps://doi.org/10.1016/j.soilbio.2020.108116openalex-snapshot
Glomalin – Truths, myths, and the future of this elusive soil glycoprotein
inferred← citeshttps://doi.org/10.1016/j.soilbio.2022.108615openalex-snapshot
Microbial carbon use efficiency and priming of soil organic matter mineralization by glucose additions in boreal forest soils with different C:N ratios
inferred← citeshttps://doi.org/10.1016/j.tplants.2008.11.004openalex-snapshot
Green plants that feed on fungi: facts and questions about mixotrophy
inferred← citeshttps://doi.org/10.1016/j.tree.2006.07.003openalex-snapshot
Mycorrhizal networks: des liaisons dangereuses?
inferred← citeshttps://doi.org/10.1016/j.tree.2010.05.004openalex-snapshot
Rooting theories of plant community ecology in microbial interactions
inferred← citeshttps://doi.org/10.1016/j.trip.2025.101618openalex-snapshot
Mycomobility: Analysis of human transport through a mycorrhizal analogy
inferred← citeshttps://doi.org/10.1017/9781108612265openalex-snapshot
The Nature of Plant Communities
inferred← citeshttps://doi.org/10.1017/9781108612265.001openalex-snapshot
Preface
inferred← citeshttps://doi.org/10.1017/9781108612265.002openalex-snapshot
Glossary
inferred← citeshttps://doi.org/10.1017/9781108612265.003openalex-snapshot
Plants Are Strange and Wondrous Beings
inferred← citeshttps://doi.org/10.1017/9781108612265.004openalex-snapshot
Interactions between Species
inferred← citeshttps://doi.org/10.1017/9781108612265.005openalex-snapshot
Mechanisms of Coexistence
inferred← citeshttps://doi.org/10.1017/9781108612265.006openalex-snapshot
Community-Level Processes
inferred← citeshttps://doi.org/10.1017/9781108612265.007openalex-snapshot
Assembly Rules
inferred← citeshttps://doi.org/10.1017/9781108612265.008openalex-snapshot
Theories and Their Predictions
inferred← citeshttps://doi.org/10.1017/9781108612265.009openalex-snapshot
Synthesis
inferred← citeshttps://doi.org/10.1017/9781108612265.010openalex-snapshot
Subject Index
inferred← citeshttps://doi.org/10.1017/9781108612265.011openalex-snapshot
Taxonomic Index
inferred← citeshttps://doi.org/10.1017/cbo9780511541797.009openalex-snapshot
Mycorrhizas and the terrestrial carbon cycle: roles in global carbon sequestration and plant community composition
inferred← citeshttps://doi.org/10.1017/cbo9781107110632.010openalex-snapshot
Constraints on Nutrient Dynamics in Terrestrial Vegetation
inferred← citeshttps://doi.org/10.1038/nplants.2015.159openalex-snapshot
Regulation of resource exchange in the arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1038/s41598-026-56653-9openalex-snapshot
Evidence for resource transfer via common endophyte networks
inferred← citeshttps://doi.org/10.1038/s42003-018-0201-9openalex-snapshot
Mycorrhizal fungi mediate the direction and strength of plant–soil feedbacks differently between arbuscular mycorrhizal and ectomycorrhizal communities
inferred← citeshttps://doi.org/10.1055/s-2005-872981openalex-snapshot
The Plant's Capacity in Regulating Resource Demand
inferred← citeshttps://doi.org/10.1071/bt16125openalex-snapshot
Comparison of two monodominant species in New Caledonia: floristic diversity and ecological strategies of Arillastrum gummiferum (Myrtaceae) and Nothofagus aequilateralis (Nothofagaceae) rainforests
inferred← citeshttps://doi.org/10.1071/sr19067openalex-snapshot
Soil biodiversity and biogeochemical function in managed ecosystems
inferred← citeshttps://doi.org/10.1073/pnas.2221619120openalex-snapshot
Climate change–induced stress disrupts ectomycorrhizal interaction networks at the boreal–temperate ecotone
inferred← citeshttps://doi.org/10.1080/00103620903563964openalex-snapshot
Uptake of Arsenic by Maize Inoculated with Three Different Arbuscular Mycorrhizal Fungi
inferred← citeshttps://doi.org/10.1080/03650340.2020.1834536openalex-snapshot
Glomalin contribution to soil organic carbon under different pasture managements in a saline soil environment
inferred← citeshttps://doi.org/10.1080/14427591.2024.2346177openalex-snapshot
Occupational security: A holistic values-based framework for supporting occupations and safety
inferred← citeshttps://doi.org/10.1080/17550874.2013.848950openalex-snapshot
Mycorrhizal ecology on serpentine soils
inferred← citeshttps://doi.org/10.1086/657955openalex-snapshot
The Effects of Above- and Belowground Mutualisms on Orchid Speciation and Coexistence
inferred← citeshttps://doi.org/10.1086/696686openalex-snapshot
Mycorrhizal Network Connections, Water Reduction, and Neighboring Plant Species Differentially Impact Seedling Performance of Two Forest Wildflowers
inferred← citeshttps://doi.org/10.1093/aobpla/plac043openalex-snapshot
Molinia caerulea alters forest Quercus petraea seedling growth through reduced mycorrhization
inferred← citeshttps://doi.org/10.1093/aobpla/plw084openalex-snapshot
Loss of functional diversity and network modularity in introduced plant-fungal symbioses
inferred← citeshttps://doi.org/10.1093/femsre/fuaf009openalex-snapshot
Electrical signaling in fungi: past and present challenges
inferred← citeshttps://doi.org/10.1093/forestscience/53.6.635openalex-snapshot
Ectomycorrhizal Communities on Tree Roots and in Soil Propagule Banks along a Secondary Successional Vegetation Gradient
inferred← citeshttps://doi.org/10.1093/jpe/rtp015openalex-snapshot
Use of 15N stable isotope to quantify nitrogen transfer between mycorrhizal plants
inferred← citeshttps://doi.org/10.1093/jpe/rtw123openalex-snapshot
Competition for resources is ameliorated by niche differentiation between Solidago virgaurea life-history stages in the Arctic
inferred← citeshttps://doi.org/10.1093/jxb/erp144openalex-snapshot
Natural selection and the evolutionary ecology of the arbuscular mycorrhizal fungi (Phylum Glomeromycota)
inferred← citeshttps://doi.org/10.1093/oso/9780198832997.003.0005openalex-snapshot
Enhancing General Resilience in Forests
inferred← citeshttps://doi.org/10.1093/treephys/27.1.133openalex-snapshot
Physiological and phenological responses of oak seedlings to oak forest soil in the absence of trees
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