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Epiparasitic plants specialized on arbuscular mycorrhizal fungi
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/mpev.2001.1007openalex-snapshot
Glomus, the Largest Genus of the Arbuscular Mycorrhizal Fungi (Glomales), Is Nonmonophyletic
inferredcites →https://doi.org/10.1007/978-1-4020-6754-9_12413openalex-snapshot
PAUP (phylogenetic analysis using parsimony)
inferredcites →https://doi.org/10.1007/s005720000061openalex-snapshot
Specific PCR primers to identify arbuscular mycorrhizal fungi within colonized roots
inferredcites →https://doi.org/10.1007/s005720100099openalex-snapshot
Identification of a mycorrhizal fungus in the roots of achlorophyllous Sciaphila tosaensis Makino (Triuridaceae)
inferredcites →https://doi.org/10.1016/0168-9525(90)90186-aopenalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/0307-4412(91)90165-5openalex-snapshot
PCR Protocols-A Guide to Methods and Applications
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/s0065-2296(08)60055-5openalex-snapshot
Mutualism and Parasitism: Diversity in Function and Structure in the “Arbuscular” (VA) Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/s0953-7562(09)81272-0openalex-snapshot
Ecological specificity of vesicular-arbuscular mycorrhizal associations
inferredcites →https://doi.org/10.1038/23932openalex-snapshot
Mycorrhizal fungal diversity determines plant biodiversity, ecosystem variability and productivity
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/10.1046/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.1365-294x.1999.00535.xopenalex-snapshot
Intrasporal variability of ribosomal sequences in the endomycorrhizal fungus Gigaspora margarita
inferredcites →https://doi.org/10.1046/j.1365-294x.1999.00604.xopenalex-snapshot
Molecular diversity of arbuscular mycorrhizal fungi colonising Hyacinthoides non‐scripta (bluebell) in a seminatural woodland
inferredcites →https://doi.org/10.1046/j.1365-294x.2001.01358.xopenalex-snapshot
Extreme specificity in epiparasitic Monotropoideae (Ericaceae): widespread phylogenetic and geographical structure
inferredcites →https://doi.org/10.1046/j.1469-8137.1997.00729.xopenalex-snapshot
Functioning of mycorrhizal associations along the mutualism–parasitism continuum*
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/10.1073/pnas.94.9.4510openalex-snapshot
Independent, specialized invasions of ectomycorrhizal mutualism by two nonphotosynthetic orchids
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/10.1111/j.1365-294x.1993.tb00005.xopenalex-snapshot
ITS primers with enhanced specificity for basidiomycetes ‐ application to the identification of mycorrhizae and rusts
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.1438-8677.1997.tb00643.xopenalex-snapshot
Root Anatomy and Mycotrophy of the Achlorophyllous Voyria tenella Hook. (Gentianaceae)
inferredcites →https://doi.org/10.1111/j.1469-8137.1994.tb04272.xopenalex-snapshot
The biology of myco‐heterotrophic (‘saprophytic’) plants
inferredcites →https://doi.org/10.2307/1941453openalex-snapshot
Plant and Soil Controls on Mycorrhizal Fungal Communities
inferredcites →https://doi.org/10.2307/2261701openalex-snapshot
Host-Dependent Sporulation and Species Diversity of Arbuscular Mycorrhizal Fungi in a Mown Grassland
inferredcites →https://doi.org/10.2307/3761561openalex-snapshot
Molecular Phylogeny of the Arbuscular Mycorrhizal Fungi Glomus sinuosum and Sclerocystis coremioides
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/tax.12765zenodo-depositor-declared
Unravelling the species diversity, phylogeny and biogeography of the mycoheterotrophic Voyrieae (Gentianaceae) and the description of a new species
inferred← citeshttps://doi.org/10.1002/9781118314364.ch5openalex-snapshot
Biology of Mycoheterotrophic and Mixotrophic Plants
inferred← citeshttps://doi.org/10.1002/ece3.2974openalex-snapshot
Fungal‐host diversity among mycoheterotrophic plants increases proportionally to their fungal‐host overlap
inferred← citeshttps://doi.org/10.1002/ecs2.4296openalex-snapshot
Microclimate, soil chemistry, and microbiota fail to explain Euphorbia dendroides Janzen‐Connell pattern in a shrubland
inferred← citeshttps://doi.org/10.1002/jobm.202200463openalex-snapshot
Transcriptome analysis of Armillaria gallica 012 m in response to auxin
inferred← citeshttps://doi.org/10.1002/ppp3.10092openalex-snapshot
Mycorrhizas for a changing world: Sustainability, conservation, and society
inferred← citeshttps://doi.org/10.1002/ppp3.70107openalex-snapshot
Range‐wide sampling reveals cryptic lineages but largely conserved mycorrhizal associations in the Japanese fairy lantern Thismia kobensis
inferred← citeshttps://doi.org/10.1002/tax.593015openalex-snapshot
The reproductive biology of Voyria (Gentianaceae) species in French Guiana
inferred← citeshttps://doi.org/10.1007/3-540-27043-4_16openalex-snapshot
Tracing the Behaviour of Plants in Ecosystems: How Can Molecular Ecology Help?
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_1openalex-snapshot
Mycoheterotrophy: An Introduction
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_2openalex-snapshot
Taxonomy and Classification
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_3openalex-snapshot
Biogeography and Conservation
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_4openalex-snapshot
Subterranean Morphology and Mycorrhizal Structures
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_5openalex-snapshot
Evolution and Diversification
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_7openalex-snapshot
Species Interactions of Mycoheterotrophic Plants: Specialization and its Potential Consequences
inferred← citeshttps://doi.org/10.1007/978-1-4614-5209-6_8openalex-snapshot
The Physiological Ecology of Mycoheterotrophy
inferred← citeshttps://doi.org/10.1007/978-3-030-15228-4_3openalex-snapshot
Biodiversity of Arbuscular Mycorrhizal Fungi in South America: A Review
inferred← citeshttps://doi.org/10.1007/978-3-030-87512-1_9openalex-snapshot
Microbe-Induced Plant Volatiles and Their Role in Plant Disease Management
inferred← citeshttps://doi.org/10.1007/978-3-031-12994-0_14openalex-snapshot
Mycorrhizas in Nothofagus From South America: What Do We Know From Nursery and Field Experiences?
inferred← citeshttps://doi.org/10.1007/978-3-032-16045-4_2openalex-snapshot
Linkages Between Mycorrhizae Fungi Diversity and Plants Adaptation in Semiarid Region: A Smart Alliance in Harsh Conditions
inferred← citeshttps://doi.org/10.1007/978-3-319-57849-1_1openalex-snapshot
Carbon Fluxes in Mycorrhizal Plants
inferred← citeshttps://doi.org/10.1007/978-3-319-57849-1_10openalex-snapshot
Mycorrhizal Symbiosis: Ways Underlying Plant–Fungus Interactions
inferred← citeshttps://doi.org/10.1007/978-3-319-68867-1_8openalex-snapshot
Mycorrhizal Fungi as Control Agents Against Plant Pathogens
inferred← citeshttps://doi.org/10.1007/978-3-540-78826-3_5openalex-snapshot
Global Diversity Patterns of Arbuscular Mycorrhizal Fungi–Community Composition and Links with Functionality
inferred← citeshttps://doi.org/10.1007/978-3-642-15271-9_6openalex-snapshot
Role of Mycorrhizal Symbioses in Phosphorus Cycling
inferred← citeshttps://doi.org/10.1007/978-3-642-54010-3_12openalex-snapshot
The Role of Arbuscular Mycorrhiza in the Growth and Development of Plants in the Family Gentianaceae
inferred← citeshttps://doi.org/10.1007/978-3-642-54010-3_2openalex-snapshot
Classification and Evolution of the Family Gentianaceae
inferred← citeshttps://doi.org/10.1007/978-3-662-54787-8_2openalex-snapshot
Extreme Organismen und Transspermie
inferred← citeshttps://doi.org/10.1007/978-3-662-59492-6_2openalex-snapshot
Extreme Organismen und Transspermie
inferred← citeshttps://doi.org/10.1007/978-94-007-2214-9_13openalex-snapshot
Tripartite Association Among Plant, Arbuscular Mycorrhizal Fungi and Bacteria
inferred← citeshttps://doi.org/10.1007/978-94-017-7395-9_2openalex-snapshot
Functional Significance of Anastomosis in Arbuscular Mycorrhizal Networks
inferred← citeshttps://doi.org/10.1007/978-981-16-8877-5_16openalex-snapshot
Arbuscular Mycorrhizal Fungi Influence Crop Productivity, Plant Diversity, and Ecosystem Services
inferred← citeshttps://doi.org/10.1007/978-981-19-4101-6_6openalex-snapshot
Arbuscular Mycorrhizal Fungal Symbiosis for Mutual Benefit: More Than Expectation
inferred← citeshttps://doi.org/10.1007/bf02803144openalex-snapshot
Molecular identification of arbuscular mycorrhizal fungi in roots: Perspectives and problems
inferred← citeshttps://doi.org/10.1007/bf02803150openalex-snapshot
Establishment of mycorrhizal symbiosis inGentiana verna
inferred← citeshttps://doi.org/10.1007/s00248-013-0229-9openalex-snapshot
Ectomycorrhizas Naturally Established in Nothofagus nervosa Seedlings Under Different Cultivation Practices in a Forest Nursery
inferred← citeshttps://doi.org/10.1007/s00425-004-1436-xopenalex-snapshot
Molecular and cell biology of arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1007/s00442-014-3137-xopenalex-snapshot
Partial mycoheterotrophy in Pyroleae: nitrogen and carbon stable isotope signatures during development from seedling to adult
inferred← citeshttps://doi.org/10.1007/s00442-020-04631-xopenalex-snapshot
Isotopic evidence of arbuscular mycorrhizal cheating in a grassland gentian species
inferred← citeshttps://doi.org/10.1007/s00572-003-0255-4openalex-snapshot
A dorsiventral mycorrhizal root in the achlorophyllous Sciaphila polygyna (Triuridaceae)
inferred← citeshttps://doi.org/10.1007/s00572-006-0080-7openalex-snapshot
Host-related variability in arbuscular mycorrhizal fungal structures in roots of Hedera rhombea, Rubus parvifolius, and Rosa multiflora under controlled conditions
inferred← citeshttps://doi.org/10.1007/s00572-007-0147-0openalex-snapshot
The cultivation bias: different communities of arbuscular mycorrhizal fungi detected in roots from the field, from bait plants transplanted to the field, and from a greenhouse trap experiment
inferred← citeshttps://doi.org/10.1007/s00572-008-0179-0openalex-snapshot
Rutaceae sampled from Germany, Malta, and Mallorca (Spain) are associated with AMF clustering with Glomus hoi Berch & Trappe
inferred← citeshttps://doi.org/10.1007/s00572-011-0373-3openalex-snapshot
Specific arbuscular mycorrhizal fungi associated with non-photosynthetic Petrosavia sakuraii (Petrosaviaceae)
inferred← citeshttps://doi.org/10.1007/s00572-011-0419-6openalex-snapshot
Arbuscular mycorrhizal fungi in national parks, nature reserves and protected areas worldwide: a strategic perspective for their in situ conservation
inferred← citeshttps://doi.org/10.1007/s00572-012-0462-yopenalex-snapshot
Enkianthus campanulatus (Ericaceae) is commonly associated with arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1007/s00572-016-0680-9openalex-snapshot
Distribution of Petrosavia sakuraii (Petrosaviaceae), a rare mycoheterotrophic plant, may be determined by the abundance of its mycobionts
inferred← citeshttps://doi.org/10.1007/s00572-020-00997-1openalex-snapshot
Ignored diversity of arbuscular mycorrhizal fungi in co-occurring mycotrophic and non-mycotrophic plants
inferred← citeshttps://doi.org/10.1007/s00572-020-01002-5openalex-snapshot
Mycorrhizal communities of two closely related species, Pyrola subaphylla and P. japonica, with contrasting degrees of mycoheterotrophy in a sympatric habitat
inferred← citeshttps://doi.org/10.1007/s00572-021-01055-0openalex-snapshot
Elevational distribution and occurrence of arbuscular mycorrhizal fungi in non-host Carex capillacea
inferred← citeshttps://doi.org/10.1007/s00572-023-01121-9openalex-snapshot
Association of mycoheterotrophic Gentianaceae with specific Glomus lineages
inferred← citeshttps://doi.org/10.1007/s00572-026-01271-6openalex-snapshot
Partial mycoheterotrophy in the arbuscular mycorrhizal Gentiana squarrosa (Gentianaceae) demonstrated by coculture assays using C3 and C4 plants
inferred← citeshttps://doi.org/10.1007/s10265-009-0234-8openalex-snapshot
Phylogenetic affinity of arbuscular mycorrhizal symbionts in Psilotum nudum
inferred← citeshttps://doi.org/10.1007/s10265-010-0395-5openalex-snapshot
Rate accelerations in nuclear 18S rDNA of mycoheterotrophic and parasitic angiosperms
inferred← citeshttps://doi.org/10.1007/s10265-014-0661-zopenalex-snapshot
Significant difference in mycorrhizal specificity between an autotrophic and its sister mycoheterotrophic plant species of Petrosaviaceae
inferred← citeshttps://doi.org/10.1007/s10265-021-01311-6openalex-snapshot
Mycoheterotrophic seedling growth of Gentiana zollingeri, a photosynthetic Gentianaceae plant species, in symbioses with arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1007/s10265-023-01496-yopenalex-snapshot
Impact of mycoheterotrophy on the growth of Gentiana zollingeri (Gentianaceae), as suggested by size variation, morphology, and 13C abundance of flowering shoots
inferred← citeshttps://doi.org/10.1007/s10267-010-0084-1openalex-snapshot
Arbuscular mycorrhizal fungi in roots of non-photosynthetic plants, Sciaphila japonica and Sciaphila tosaensis (Triuridaceae)
inferred← citeshttps://doi.org/10.1007/s11104-005-4826-3openalex-snapshot
Arbuscular Mycorrhizal Assemblages in Native Plant Roots Change in the Presence of Invasive Exotic Grasses
inferred← citeshttps://doi.org/10.1007/s11104-009-9925-0openalex-snapshot
Carbon flow in the rhizosphere: carbon trading at the soil–root interface
inferred← citeshttps://doi.org/10.1007/s11104-019-04063-4openalex-snapshot
Arbuscular mycorrhizal fungi protect native woody species from novel weapons
inferred← citeshttps://doi.org/10.1007/s11104-020-04694-yopenalex-snapshot
Changes in the mycorrhizal fungal community in host roots over five host generations under low and high phosphorus conditions
inferred← citeshttps://doi.org/10.1007/s11104-023-06045-zopenalex-snapshot
Arbuscular mycorrhiza: advances and retreats in our understanding of the ecological functioning of the mother of all root symbioses
inferred← citeshttps://doi.org/10.1007/s11258-005-9037-8openalex-snapshot
Differential host plant performance as a function of soil arbuscular mycorrhizal fungal communities: experimentally manipulating co-occurring Glomus species
inferred← citeshttps://doi.org/10.1007/s11368-010-0239-xopenalex-snapshot
Soil fungal communities differ in native mixed forest and adjacent Araucaria cunninghamii plantations in subtropical Australia
inferred← citeshttps://doi.org/10.1007/s11557-006-0500-2openalex-snapshot
Arbuscular mycorrhizal fungi of the Glomus-group A lineage (Glomerales; Glomeromycota) detected in myco-heterotrophic plants from tropical Africa
inferred← citeshttps://doi.org/10.1007/s12225-019-9833-2openalex-snapshot
Arachnitis uniflora: first report of Corsiaceae for the Peruvian Flora
inferred← citeshttps://doi.org/10.1007/s13213-015-1097-yopenalex-snapshot
Colonization and molecular diversity of arbuscular mycorrhizal fungi associated with the rhizosphere of cowpea (Vigna unguiculata (L.) Walp.) in Benin (West Africa): an exploratory study
inferred← citeshttps://doi.org/10.1007/s13213-015-1116-zopenalex-snapshot
Metadata-mining of 18S rDNA sequences reveals that “everything is not everywhere” for glomeromycotan fungi
inferred← citeshttps://doi.org/10.1007/s40502-019-00491-7openalex-snapshot
Interplant communication via hyphal networks
inferred← citeshttps://doi.org/10.1016/b978-0-12-819590-1.00011-2openalex-snapshot
Fluxes of nutrients in mycorrhiza: what has fluxomics taught us in the plant-fungus interaction?
inferred← citeshttps://doi.org/10.1016/j.biortech.2023.129395openalex-snapshot
Plant -microbe assisted emerging contaminants (ECs) removal and carbon cycling
inferred← citeshttps://doi.org/10.1016/j.envpol.2004.11.002openalex-snapshot
Diversity of arbuscular mycorrhizal fungi in grassland spontaneously developed on area polluted by a fertilizer plant
inferred← citeshttps://doi.org/10.1016/j.funeco.2010.02.002openalex-snapshot
Nutritional ecology of arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/j.funeco.2015.05.011openalex-snapshot
Ectomycorrhizal fungal communities in Nothofagus nervosa ( Raulí ): A comparison between domesticated and naturally established specimens in a native forest of Patagonia, Argentina
inferred← citeshttps://doi.org/10.1016/j.funeco.2022.101211openalex-snapshot
Plant community and soil available nutrients drive arbuscular mycorrhizal fungal community shifts during alpine meadow degradation
inferred← citeshttps://doi.org/10.1016/j.gloplacha.2021.103701openalex-snapshot
Ancient climate changes and Andes uplift, rather than Last Glacial Maximum, affected distribution and genetic diversity patterns of the southernmost mycoheterotrophic plant Arachnitis uniflora Phil. (Corsiaceae)
inferred← citeshttps://doi.org/10.1016/j.jaridenv.2005.05.002openalex-snapshot
Arbuscular mycorrhizae from arid parts of Namibia
inferred← citeshttps://doi.org/10.1016/j.myc.2013.02.004openalex-snapshot
High mycorrhizal specificity in the mycoheterotrophic Burmannia nepalensis and B. itoana (Burmanniaceae)
inferred← citeshttps://doi.org/10.1016/j.mycres.2006.04.005openalex-snapshot
Phylogenetic analysis of nuclear small subunit rDNA sequences suggests that the endangered African Pencil Cedar, Juniperus procera, is associated with distinct members of Glomeraceae
inferred← citeshttps://doi.org/10.1016/j.pbi.2004.04.004openalex-snapshot
Myco-heterotroph/epiparasitic plant interactions with ectomycorrhizal and arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/j.pbi.2006.05.001openalex-snapshot
Endophyte or parasite – what decides?
inferred← citeshttps://doi.org/10.1016/j.ppees.2011.02.002openalex-snapshot
The evolutionary ecology of dust seeds
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101205openalex-snapshot
Lessons from mycorrhizal Synergies: Broad-Leaved trees Boost Chinese fir resilience
inferred← citeshttps://doi.org/10.1016/j.scitotenv.2017.01.049openalex-snapshot
Spatiotemporal variation of arbuscular mycorrhizal fungal colonization in olive ( Olea europaea L.) roots across a broad mesic-xeric climatic gradient in North Africa
inferred← citeshttps://doi.org/10.1016/j.soilbio.2009.08.001openalex-snapshot
Converting Australian tropical rainforest to native Araucariaceae plantations alters soil fungal communities
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.tree.2006.07.003openalex-snapshot
Mycorrhizal networks: des liaisons dangereuses?
inferred← citeshttps://doi.org/10.1016/s0167-7799(03)00204-xopenalex-snapshot
Cultivation of edible ectomycorrhizal mushrooms
inferred← citeshttps://doi.org/10.1016/s0275-0287(08)80055-0openalex-snapshot
Chapter 13 Responses of mycorrhizal fungi to stress
inferred← citeshttps://doi.org/10.1016/s1360-1385(03)00012-8openalex-snapshot
Preference, specificity and cheating in the arbuscular mycorrhizal symbiosis
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/cbo9780511541926.013openalex-snapshot
Is diversity of mycorrhizal fungi important for ecosystem functioning?
inferred← citeshttps://doi.org/10.1017/cbo9780511541971.008openalex-snapshot
Mycorrhizas and ecosystem processes in tropical rain forest: implications for diversity
inferred← citeshttps://doi.org/10.1017/s0269-915x(04)00205-8openalex-snapshot
Mycorrhizal fungi and their multifunctional roles
inferred← citeshttps://doi.org/10.1017/s0269-915x(05)00301-0openalex-snapshot
Mycorrhizal symbiosis: myths, misconceptions, new perspectives and future research priorities
inferred← citeshttps://doi.org/10.1017/s0269-915x(05)00302-2openalex-snapshot
The ecology and evolution of the arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1017/s0269-915x(05)00304-6openalex-snapshot
Plants parasitic on fungi: unearthing the fungi in myco-heterotrophs and debunking the ‘saprophytic’ plant myth
inferred← citeshttps://doi.org/10.1017/s0953756202007116openalex-snapshot
Ectomycorrhizas involving sebacinoid mycobionts
inferred← citeshttps://doi.org/10.1017/s0953756202237132openalex-snapshot
Mycorrhizas of Non-Photosynthetic Plants
inferred← citeshttps://doi.org/10.1017/s1464793103006316openalex-snapshot
Diversity and classification of mycorrhizal associations
inferred← citeshttps://doi.org/10.1023/a:1025695032113openalex-snapshot
Review Paper: Arbuscular Mycorrhiza: Biological, Chemical, and Molecular Aspects
inferred← citeshttps://doi.org/10.1038/ncomms1105openalex-snapshot
Mutualistic mycorrhiza-like symbiosis in the most ancient group of land plants
inferred← citeshttps://doi.org/10.1038/news020923-7openalex-snapshot
Vegetal vampires stalk South America
inferred← citeshttps://doi.org/10.1038/nrmicro1987openalex-snapshot
Arbuscular mycorrhiza: the mother of plant root endosymbioses
inferred← citeshttps://doi.org/10.1038/s41467-020-16507-yopenalex-snapshot
Soil fungal networks maintain local dominance of ectomycorrhizal trees
inferred← citeshttps://doi.org/10.1038/s41467-022-34416-0openalex-snapshot
Ancient oral microbiomes support gradual Neolithic dietary shifts towards agriculture
inferred← citeshttps://doi.org/10.1038/s41477-022-01127-9openalex-snapshot
Genomes of leafy and leafless Platanthera orchids illuminate the evolution of mycoheterotrophy
inferred← citeshttps://doi.org/10.1038/s41477-024-01677-0openalex-snapshot
Mycoheterotrophy in the wood-wide web
inferred← citeshttps://doi.org/10.1046/j.1365-294x.2003.01967.xopenalex-snapshot
Co‐existing grass species have distinctive arbuscular mycorrhizal communities
inferred← citeshttps://doi.org/10.1046/j.1461-0248.2003.00400.xopenalex-snapshot
Phoenix clones: recovery after long‐term defoliation‐induced dormancy
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00876.xopenalex-snapshot
Nitrogen and carbon stable isotope abundances support the myco‐heterotrophic nature and host‐specificity of certain achlorophyllous plants
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00917.xopenalex-snapshot
Divergent arbuscular mycorrhizal fungal communities colonize roots of Pulsatilla spp. in boreal Scots pine forest and grassland soils
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00924.xopenalex-snapshot
Molecular diversity of arbuscular mycorrhizal fungi in Prunus africana, an endangered medicinal tree species in dry Afromontane forests of Ethiopia
inferred← citeshttps://doi.org/10.1046/j.1469-8137.2003.00938.xopenalex-snapshot
Plant communities affect arbuscular mycorrhizal fungal diversity and community composition in grassland microcosms
inferred← citeshttps://doi.org/10.1055/s-2007-965613openalex-snapshot
Specialized Mycorrhizal Colonization Pattern in AchlorophyllousEpirixanthesspp. (Polygalaceae)
inferred← citeshttps://doi.org/10.1080/01490451003702958openalex-snapshot
Mineral Transformations by Mycorrhizal Fungi
inferred← citeshttps://doi.org/10.1080/15572536.2005.11832912openalex-snapshot
The southernmost myco-heterotrophic plant,Arachnitis uniflora: root morphology and anatomy
inferred← citeshttps://doi.org/10.1080/15572536.2006.11832656openalex-snapshot
Monotropa uniflora plants of eastern Massachusetts form mycorrhizae with a diversity of russulacean fungi
inferred← citeshttps://doi.org/10.1080/17429145.2010.541945openalex-snapshot
The parasitic mechanism of the holostemparasitic plantCuscuta
inferred← citeshttps://doi.org/10.1093/acprof:oso/9780199228973.001.0001openalex-snapshot
Community Ecology
inferred← citeshttps://doi.org/10.1093/aob/mcp235openalex-snapshot
Myco-heterotrophy: when fungi host plants
inferred← citeshttps://doi.org/10.1093/aob/mcw119openalex-snapshot
Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi
inferred← citeshttps://doi.org/10.1093/aob/mcx023openalex-snapshot
Genetic diversity patterns of arbuscular mycorrhizal fungi associated with the mycoheterotroph Arachnitis uniflora Phil. (Corsiaceae)
inferred← citeshttps://doi.org/10.1093/jpe/rtad042openalex-snapshot
Asymmetric and uncertain interactions within mutualisms
inferred← citeshttps://doi.org/10.1093/jpe/rtx038openalex-snapshot
Arbuscular mycorrhizal fungi differ in affecting the flowering of a host plant under two soil phosphorus conditions
inferred← citeshttps://doi.org/10.1093/jxb/eri192openalex-snapshot
How do plants regulate the function, community structure, and diversity of mycorrhizal fungi?
inferred← citeshttps://doi.org/10.1093/jxb/erm366openalex-snapshot
Deception above, deception below: linking pollination and mycorrhizal biology of orchids
inferred← citeshttps://doi.org/10.1093/jxb/ern059openalex-snapshot
Ecological aspects of mycorrhizal symbiosis: with special emphasis on the functional diversity of interactions involving the extraradical mycelium
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/9780198797876.003.0007openalex-snapshot
How to be a plant macroparasite
inferred← citeshttps://doi.org/10.1098/rspb.2002.2299openalex-snapshot
Specialized cheating of the ectomycorrhizal symbiosis by an epiparasitic liverwort
inferred← citeshttps://doi.org/10.1098/rspb.2003.2557openalex-snapshot
Evidence for mycorrhizal races in a cheating orchid
inferred← citeshttps://doi.org/10.1098/rspb.2004.2807openalex-snapshot
Changing partners in the dark: isotopic and molecular evidence of ectomycorrhizal liaisons between forest orchids and trees
inferred← citeshttps://doi.org/10.1098/rspb.2007.1622openalex-snapshot
Breakdown and delayed cospeciation in the arbuscular mycorrhizal mutualism
inferred← citeshttps://doi.org/10.1098/rspb.2008.1225openalex-snapshot
Evidence for novel and specialized mycorrhizal parasitism: the orchid Gastrodia confusa gains carbon from saprotrophic Mycena
inferred← citeshttps://doi.org/10.1098/rspb.2009.1190openalex-snapshot
Evidence of a myco-heterotroph in the plant family Ericaceae that lacks mycorrhizal specificity
inferred← citeshttps://doi.org/10.1098/rspb.2016.2093openalex-snapshot
A phosphorus threshold for mycoheterotrophic plants in tropical forests
inferred← citeshttps://doi.org/10.1098/rspb.2020.0483openalex-snapshot
Shifts in plant community composition weaken the negative effect of nitrogen addition on community-level arbuscular mycorrhizal fungi colonization
inferred← citeshttps://doi.org/10.1101/867259openalex-snapshot
Antagonistic plants preferentially target arbuscular mycorrhizal fungi that are highly connected to mutualistic plants
inferred← citeshttps://doi.org/10.1104/pp.111.177618openalex-snapshot
Carbon and Nitrogen Metabolism in Mycorrhizal Networks and Mycoheterotrophic Plants of Tropical Forests: A Stable Isotope Analysis
inferred← citeshttps://doi.org/10.1104/pp.112.195727openalex-snapshot
Mycorrhizal Networks: Common Goods of Plants Shared under Unequal Terms of Trade
inferred← citeshttps://doi.org/10.1111/1365-2435.14706openalex-snapshot
Not only transitions in nutritional modes but also niche shifts facilitate mycorrhizal fungal specialization in Burmannia
inferred← citeshttps://doi.org/10.1111/1365-2745.13381openalex-snapshot
Mycoheterotrophic plants living on arbuscular mycorrhizal fungi are generally enriched in 13C, 15N and 2H isotopes
inferred← citeshttps://doi.org/10.1111/1462-2920.15781openalex-snapshot
Symbiotic germination and development of fully mycoheterotrophic plants convergently targeting similar Glomeraceae taxa
inferred← citeshttps://doi.org/10.1111/ele.12115openalex-snapshot
Underground signals carried through common mycelial networks warn neighbouring plants of aphid attack
inferred← citeshttps://doi.org/10.1111/ele.12939openalex-snapshot
Partitioning of soil phosphorus among arbuscular and ectomycorrhizal trees in tropical and subtropical forests
inferred← citeshttps://doi.org/10.1111/geb.12920openalex-snapshot
Global distribution patterns of mycoheterotrophy
inferred← citeshttps://doi.org/10.1111/j.1096-0031.2008.00241.xopenalex-snapshot
Bias and conflict in phylogenetic inference of myco‐heterotrophic plants: a case study in Thismiaceae
inferred← citeshttps://doi.org/10.1111/j.1365-2745.2006.01136.xopenalex-snapshot
Composition of root‐colonizing arbuscular mycorrhizal fungal communities in different ecosystems around the globe
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02223.xopenalex-snapshot
Differences in mycorrhizal preferences between two tropical orchids
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2004.02350.xopenalex-snapshot
Strong fungal specificity and selectivity for algal symbionts in Florida scrubCladonialichens
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2005.02503.xopenalex-snapshot
On the origins of extreme mycorrhizal specificity in the Monotropoideae (Ericaceae): performance trade‐offs during seed germination and seedling development
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2005.02770.xopenalex-snapshot
Inefficient photosynthesis in the Mediterranean orchid Limodorum abortivum is mirrored by specific association to ectomycorrhizal Russulaceae
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2006.02921.xopenalex-snapshot
Communities of arbuscular mycorrhizal fungi in arable soils are not necessarily low in diversity
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2011.05000.xopenalex-snapshot
Mycorrhizal specificity in the fully mycoheterotrophic Hexalectris Raf. (Orchidaceae: Epidendroideae)
inferred← citeshttps://doi.org/10.1111/j.1365-294x.2012.05472.xopenalex-snapshot
Mycoheterotrophic interactions are not limited to a narrow phylogenetic range of arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1111/j.1365-3040.2005.01378.xopenalex-snapshot
A unique mode of parasitism in the conifer coral treeParasitaxus ustus(Podocarpaceae)
inferred← citeshttps://doi.org/10.1111/j.1438-8677.2012.00680.xopenalex-snapshot
Morpho‐anatomical and molecular characterization of the mycorrhizas of European P olygala species
inferred← citeshttps://doi.org/10.1111/j.1442-1984.2012.00387.xopenalex-snapshot
Evidence for specificity to Glomus group Ab in two Asian mycoheterotrophic Burmannia species
inferred← citeshttps://doi.org/10.1111/j.1462-2920.2007.01474.xopenalex-snapshot
Relationship between assemblages of mycorrhizal fungi and bacteria on grass roots
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01114.xopenalex-snapshot
Mycorrhizal diversity in photosynthetic terrestrial orchids
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01115.xopenalex-snapshot
Symbiotic germination and development of the myco‐heterotroph Monotropa hypopitys in nature and its requirement for locally distributed Tricholoma spp.
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01145.xopenalex-snapshot
Patterns of below‐ground plant interconnections established by means of arbuscular mycorrhizal networks
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01152.xopenalex-snapshot
The fungus does not transfer carbon to or between roots in an arbuscular mycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01163.xopenalex-snapshot
Hyphal fusion to plant species connections – giant mycelia and community nutrient flow
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2004.01251.xopenalex-snapshot
The liverwort Marchantia foliacea forms a specialized symbiosis with arbuscular mycorrhizal fungi in the genus Glomus
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01429.xopenalex-snapshot
The evolutionary ecology of myco‐heterotrophy
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2005.01559.xopenalex-snapshot
‘Prepackaged symbioses’: propagules on roots of the myco‐heterotrophic plant Arachnitis uniflora
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2006.01862.xopenalex-snapshot
The mycorrhizal contribution to plant productivity, plant nutrition and soil structure in experimental grassland
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02276.xopenalex-snapshot
Arbuscular mycorrhizal associations in Lycopodiaceae
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2007.02326.xopenalex-snapshot
Conflict, cheats and the persistence of symbioses
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02352.xopenalex-snapshot
Fungal fidelity in the myco‐heterotroph‐to‐autotroph life cycle of Lycopodiaceae: a case of parental nurture?
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02353.xopenalex-snapshot
Selenium and the elemental defense hypothesis
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2008.02354.xopenalex-snapshot
Predicting evolutionary consequences of pollinator declines: the long and short of floral evolution
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03334.xopenalex-snapshot
The online database Maarj AM reveals global and ecosystemic distribution patterns in arbuscular mycorrhizal fungi (Glomeromycota)
inferred← citeshttps://doi.org/10.1111/j.1469-8137.2010.03365.xopenalex-snapshot
15N and 13C natural abundance of two mycoheterotrophic and a putative partially mycoheterotrophic species associated with arbuscular mycorrhizal fungi
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2007.00112.xopenalex-snapshot
THE EVOLUTIONARY HISTORY OF MYCORRHIZAL SPECIFICITY AMONG LADY'S SLIPPER ORCHIDS
inferred← citeshttps://doi.org/10.1111/j.1574-6941.2010.00956.xopenalex-snapshot
Plants as resource islands and storage units - adopting the mycocentric view of arbuscular mycorrhizal networks
inferred← citeshttps://doi.org/10.1111/j.1600-0706.2011.19130.xopenalex-snapshot
Life history strategy in herbaceous perennials: inferring demographic patterns from the aboveground dynamics of a primarily subterranean, myco‐heterotrophic orchid
inferred← citeshttps://doi.org/10.1111/jbi.12486openalex-snapshot
Ancient Gondwana break‐up explains the distribution of the mycoheterotrophic family Corsiaceae (Liliales)
inferred← citeshttps://doi.org/10.1111/jbi.12994openalex-snapshot
The biogeographical history of the interaction between mycoheterotrophic Thismia (Thismiaceae) plants and mycorrhizal Rhizophagus (Glomeraceae) fungi
inferred← citeshttps://doi.org/10.1111/mec.14050openalex-snapshot
Specificity of fungal associations of Pyroleae and M onotropa hypopitys during germination and seedling development
inferred← citeshttps://doi.org/10.1111/nph.13118openalex-snapshot
The fungal perspective of arbuscular mycorrhizal colonization in ‘nonmycorrhizal’ plants
inferred← citeshttps://doi.org/10.1111/nph.14249openalex-snapshot
Arbuscular mycorrhizal interactions of mycoheterotrophic Thismia are more specialized than in autotrophic plants
inferred← citeshttps://doi.org/10.1111/nph.14709openalex-snapshot
Think globally, research locally: emerging opportunities for mycorrhizal research in South America
inferred← citeshttps://doi.org/10.1111/nph.18310openalex-snapshot
Mycoheterotrophic plants preferentially target arbuscular mycorrhizal fungi that are highly connected to autotrophic plants
inferred← citeshttps://doi.org/10.1111/nph.20330openalex-snapshot
Drastic mycorrhizal community shifts in Sceptridium ferns during the generation transition from fully mycoheterotrophic gametophytes to photosynthetic sporophytes
inferred← citeshttps://doi.org/10.1111/plb.70071openalex-snapshot
Isotope evidence for partial mycoheterotrophy and trophic flexibility in the arbuscular mycorrhizal green plant Gentiana zollingeri
inferred← citeshttps://doi.org/10.1128/9781555815837.ch20openalex-snapshot
Dikaryons, Diploids, and Evolution
inferred← citeshttps://doi.org/10.1128/aem.00987-07openalex-snapshot
Cooccurring Gentiana verna and Gentiana acaulis and Their Neighboring Plants in Two Swiss Upper Montane Meadows Harbor Distinct Arbuscular Mycorrhizal Fungal Communities
inferred← citeshttps://doi.org/10.1128/aem.02889-05openalex-snapshot
Analysis of Quantitative Interactions between Two Species of Arbuscular Mycorrhizal Fungi,Glomus mosseaeandG. intraradices, by Real-Time PCR
inferred← citeshttps://doi.org/10.1128/aem.69.5.2816-2824.2003openalex-snapshot
Impact of Land Use Intensity on the Species Diversity of Arbuscular Mycorrhizal Fungi in Agroecosystems of Central Europe
inferred← citeshttps://doi.org/10.1128/aem.70.10.6240-6246.2004openalex-snapshot
Nonlegumes, Legumes, and Root Nodules Harbor Different Arbuscular Mycorrhizal Fungal Communities
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