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The importance of associations with saprotrophic non-Rhizoctoniafungi among fully mycoheterotrophic orchids is currently under-estimated: novel evidence from sub-tropical Asia

https://doi.org/10.1093/aob/mcv085
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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/tax.606003openalex-snapshot
Phylogenetic classification of Trametes (Basidiomycota, Polyporales) based on a five–marker dataset
inferredcites →https://doi.org/10.1007/0-387-33745-8openalex-snapshot
Stable Isotope Ecology
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_1openalex-snapshot
Mycoheterotrophy: An Introduction
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_8openalex-snapshot
The Physiological Ecology of Mycoheterotrophy
inferredcites →https://doi.org/10.1007/978-3-642-30826-0_12openalex-snapshot
12 Orchid Mycorrhizas: Molecular Ecology, Physiology, Evolution and Conservation Aspects
inferredcites →https://doi.org/10.1007/bf00325257openalex-snapshot
Carbon and nitrogen isotope ratios in different compartments of a healthy and a declining Picea abies forest in the Fichtelgebirge, NE Bavaria
inferredcites →https://doi.org/10.1007/bf00376940openalex-snapshot
Nitrate, nitrate reduction and organic nitrogen in plants from different ecological and taxonomic groups of Central Europe
inferredcites →https://doi.org/10.1007/bf02268616openalex-snapshot
Seed germination of Galeola altissima, an achlorophyilous orchid, with aphyllophorales fungi
inferredcites →https://doi.org/10.1007/bf02461451openalex-snapshot
Armillaria jezoensis, a new symbiont of Galeola septentrionalis (Orchidaceae)in Hokkaido
inferredcites →https://doi.org/10.1007/bf02464092openalex-snapshot
Formation of endomycorrhizas by an achlorophyllous orchid, Erythrorchis ochobiensis, and Auricularia polytricha
inferredcites →https://doi.org/10.1007/bf02464097openalex-snapshot
In vitro germination of Erythrorchis ochobiensis (Orchidaceae) in the presence of Lyophyllum shimeji, an ectomycorrhizal fungus
inferredcites →https://doi.org/10.1007/s00572-007-0138-1openalex-snapshot
Further advances in orchid mycorrhizal research
inferredcites →https://doi.org/10.1007/s00572-012-0429-zopenalex-snapshot
Mycorrhizal diversity and specificity in Lecanorchis (Orchidaceae)
inferredcites →https://doi.org/10.1007/s10267-004-0218-4openalex-snapshot
Isolation and identification of mycorrhizal fungi associating with an achlorophyllous plant, Epipogium roseum (Orchidaceae)
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/j.funeco.2009.11.003openalex-snapshot
Isotopic and molecular evidence for saprotrophic Marasmiaceae mycobionts in rhizomes of Gastrodia sesamoides
inferredcites →https://doi.org/10.1016/j.pbi.2004.04.004openalex-snapshot
Myco-heterotroph/epiparasitic plant interactions with ectomycorrhizal and arbuscular mycorrhizal fungi
inferredcites →https://doi.org/10.1016/s0953-7562(09)80415-2openalex-snapshot
Involvement of exodermal passage cells in mycorrhizal infection of some orchids
inferredcites →https://doi.org/10.1016/s1055-7903(02)00027-1openalex-snapshot
One hundred and seventeen clades of euagarics
inferredcites →https://doi.org/10.1017/cbo9780511525452openalex-snapshot
Terrestrial Orchids
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00373.xopenalex-snapshot
15N natural abundance in fruit bodies of different functional groups of fungi in relation to substrate utilization
inferredcites →https://doi.org/10.1046/j.1469-8137.2003.00872.xopenalex-snapshot
15N and 13C natural abundance of autotrophic and myco‐heterotrophic orchids provides insight into nitrogen and carbon gain from fungal association
inferredcites →https://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
inferredcites →https://doi.org/10.1071/fp08216openalex-snapshot
Why are non-photosynthetic tissues generally 13C enriched compared with leaves in C3 plants? Review and synthesis of current hypotheses
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/10.1080/10256010802507458openalex-snapshot
A methodological approach to improve estimates of nutrient gains by partially myco-heterotrophic plants†
inferredcites →https://doi.org/10.1080/10256019308046133openalex-snapshot
Nitrogen Isotope Ratios in Different Compartments of a Mixed Stand of Spruce, Larch and Beech Trees and of Understorey Vegetation Including Fungi
inferredcites →https://doi.org/10.1093/aob/mcp024openalex-snapshot
On the value of nuclear and mitochondrial gene sequences for reconstructing the phylogeny of vanilloid orchids (Vanilloideae, Orchidaceae)
inferredcites →https://doi.org/10.1093/aob/mcu240openalex-snapshot
Are carbon and nitrogen exchange between fungi and the orchid Goodyera repens affected by irradiance?
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
inferredcites →https://doi.org/10.1093/nar/25.24.4876openalex-snapshot
The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a025811openalex-snapshot
Bayesian phylogenetic inference using DNA sequences: a Markov Chain Monte Carlo Method
inferredcites →https://doi.org/10.1093/sysbio/49.2.278openalex-snapshot
Phylogenetic Relationships of Agaric Fungi Based on Nuclear Large Subunit Ribosomal DNA Sequences
inferredcites →https://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
inferredcites →https://doi.org/10.1098/rspb.2008.1225openalex-snapshot
Evidence for novel and specialized mycorrhizal parasitism: the orchid Gastrodia confusa gains carbon from saprotrophic Mycena
inferredcites →https://doi.org/10.1098/rspb.2009.1966openalex-snapshot
Irradiance governs exploitation of fungi: fine-tuning of carbon gain by two partially myco-heterotrophic orchids
inferredcites →https://doi.org/10.1104/pp.102.4.1287openalex-snapshot
Correlations between the 13C Content of Primary and Secondary Plant Products in Different Cell Compartments and That in Decomposing Basidiomycetes
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
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.1438-8677.2010.00369.xopenalex-snapshot
Stable isotope signatures confirm carbon and nitrogen gain through ectomycorrhizas in the ghost orchid Epipogium aphyllum Swartz*
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.1469-8137.2007.02065.xopenalex-snapshot
Wide geographical and ecological distribution of nitrogen and carbon gains from fungi in pyroloids and monotropoids (Ericaceae) and in orchids
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02362.xopenalex-snapshot
The ectomycorrhizal specialist orchid Corallorhiza trifida is a partial myco‐heterotroph
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02987.xopenalex-snapshot
Independent recruitment of saprotrophic fungi as mycorrhizal partners by tropical achlorophyllous orchids
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00420.xopenalex-snapshot
CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP
inferredcites →https://doi.org/10.1111/nph.12688openalex-snapshot
Carbon and nitrogen gain during the growth of orchid seedlings in nature
inferredcites →https://doi.org/10.1128/jb.172.8.4238-4246.1990openalex-snapshot
Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species
inferredcites →https://doi.org/10.1146/annurev.pp.23.060172.001133openalex-snapshot
Transfer Cells
inferredcites →https://doi.org/10.1186/1471-2105-11-7openalex-snapshot
TreeGraph 2: Combining and visualizing evidence from different phylogenetic analyses
inferredcites →https://doi.org/10.1186/1741-7007-7-51openalex-snapshot
Two mycoheterotrophic orchids from Thailand tropical dipterocarpacean forests associate with a broad diversity of ectomycorrhizal fungi
inferredcites →https://doi.org/10.2307/4615733openalex-snapshot
A Simple Sequentially Rejective Multiple Test Procedure
inferredcites →https://doi.org/10.3732/ajb.0900354openalex-snapshot
C and N stable isotope signatures reveal constraints to nutritional modes in orchids from the Mediterranean and Macaronesia
inferredcites →https://doi.org/10.3732/ajb.1100575openalex-snapshot
Limited carbon and mineral nutrient gain from mycorrhizal fungi by adult Australian orchids
inferredcites →https://doi.org/10.3732/ajb.95.1.93openalex-snapshot
High mycorrhizal specificity in a widespread mycoheterotrophic plant, Eulophia zollingeri (Orchidaceae)
inferredcites →https://doi.org/10.3852/13-003openalex-snapshot
Phylogenetic and phylogenomic overview of the Polyporales
inferredcites →https://doi.org/10.3852/mycologia.97.3.667openalex-snapshot
Phylogenetic relationships in the gymnopoid and marasmioid fungi (Basidiomycetes, euagarics clade)
inferredcites →https://doi.org/10.3852/mycologia.98.6.982openalex-snapshot
Major clades of Agaricales: a multilocus phylogenetic overview
inferredcites →https://doi.org/10.3852/mycologia.99.4.510openalex-snapshot
Mycorrhizal fungi of Vanilla: diversity, specificity and effects on seed germination and plant growth

What points at this work

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

inferred← citeshttps://doi.org/10.11646/phytotaxa.483.2.10zenodo-depositor-declared
Gastrodia qingyunshanensis (Orchidaceae: Epidendroideae)—a new holomycotrophic orchid from Guangdong, China
inferred← citeshttps://doi.org/10.1002/ajb2.1142openalex-snapshot
Partial mycoheterotrophy in the leafless orchid Cymbidium macrorhizon
inferred← citeshttps://doi.org/10.1002/ajb2.70185openalex-snapshot
Corallorhiza striata is the first example of a pseudocopulatory orchid in North America and an instance of “double deception” in fully mycoheterotrophic plants
inferred← citeshttps://doi.org/10.1002/ece3.11004openalex-snapshot
Fungal communities associated with early immature tubers of wild Gastrodia elata
inferred← citeshttps://doi.org/10.1007/978-3-319-56363-3_8openalex-snapshot
Biogeography of Orchid Mycorrhizas
inferred← citeshttps://doi.org/10.1007/978-981-99-1079-3_4openalex-snapshot
Gene Expression Profiling in Orchid Mycorrhizae to Decipher the Molecular Mechanisms of Plant–Fungus Interactions
inferred← citeshttps://doi.org/10.1007/s00572-017-0808-6openalex-snapshot
Microscopic characterization of orchid mycorrhizal fungi: Scleroderma as a putative novel orchid mycorrhizal fungus of Vanilla in different crop systems
inferred← citeshttps://doi.org/10.1007/s00572-021-01032-7openalex-snapshot
Partial and full mycoheterotrophy in green and albino phenotypes of the slipper orchid Cypripedium debile
inferred← citeshttps://doi.org/10.1007/s00572-021-01043-4openalex-snapshot
Leafless epiphytic orchids share Ceratobasidiaceae mycorrhizal fungi
inferred← citeshttps://doi.org/10.1007/s00572-023-01101-zopenalex-snapshot
Fungi in hair roots of Vaccinium spp. (Ericaceae) growing on decomposing wood: colonization patterns, identity, and in vitro symbiotic potential
inferred← citeshttps://doi.org/10.1007/s00572-025-01183-xopenalex-snapshot
The tiny-leaved orchid Disperis neilgherrensis primarily obtains carbon from decaying litter via saprotrophic Ceratobasidium
inferred← citeshttps://doi.org/10.1007/s00572-025-01208-5openalex-snapshot
Diverse mycorrhizal associations and nutrition in Didymoplexis orchids
inferred← citeshttps://doi.org/10.1007/s00572-025-01213-8openalex-snapshot
Integrated peloton and fruiting body isotope data shed light on mycoheterotrophic interactions in Gastrodia pubilabiata (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00572-026-01280-5openalex-snapshot
Isotopic and molecular evidence for contrasting fungal associations in two Epipogium orchids in cool-temperate Japan
inferred← citeshttps://doi.org/10.1007/s00572-026-01285-0openalex-snapshot
Divergent mycorrhizal strategies and nutritional modes in the East Asian orchid genus Ephippianthus
inferred← citeshttps://doi.org/10.1007/s00572-026-01286-zopenalex-snapshot
In situ seed baiting and DNA metabarcoding support developmental continuity of a Coprinellus association in the predominantly leafless orchid Cremastra aphylla
inferred← citeshttps://doi.org/10.1007/s00572-026-01288-xopenalex-snapshot
Stable isotope signatures and specific mycobionts reveal the mycoheterotrophic nutrient acquisition of Danxiaorchis yangii
inferred← citeshttps://doi.org/10.1007/s00572-026-01311-1openalex-snapshot
Integrating stable isotope and fungal association evidence for nutrient acquisition in the rare orchid, Risleya atropurpurea
inferred← citeshttps://doi.org/10.1007/s00572-026-01315-xopenalex-snapshot
Stable isotope signatures of pelotons and rhizomorphs reveal nutritional plasticity in Cremastra appendiculata (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00572-026-01320-0openalex-snapshot
Reduced fungal dependency during in situ germination of the terrestrial orchid Bletilla formosana
inferred← citeshttps://doi.org/10.1007/s10265-020-01244-6openalex-snapshot
Evolutionary histories and mycorrhizal associations of mycoheterotrophic plants dependent on saprotrophic fungi
inferred← citeshttps://doi.org/10.1007/s10265-021-01337-wopenalex-snapshot
Mycobiont diversity and first evidence of mixotrophy associated with Psathyrellaceae fungi in the chlorophyllous orchid Cremastra variabilis
inferred← citeshttps://doi.org/10.1007/s10265-021-01364-7openalex-snapshot
Weak population spatial genetic structure and low infraspecific specificity for fungal partners in the rare mycoheterotrophic orchid Epipogium aphyllum
inferred← citeshttps://doi.org/10.1007/s11557-022-01795-zopenalex-snapshot
New data in Porotheleaceae and Cyphellaceae: epitypification of Prunulus scabripes Murrill, the status of Mycopan Redhead, Moncalvo & Vilgalys and a new combination in Pleurella Horak emend.
inferred← citeshttps://doi.org/10.1007/s13199-019-00647-xopenalex-snapshot
Symbiotic fungi undergo a taxonomic and functional bottleneck during orchid seeds germination: a case study on Dendrobium moniliforme
inferred← citeshttps://doi.org/10.1016/j.funeco.2018.01.002openalex-snapshot
Seeking the needle in the haystack: Undetectability of mycorrhizal fungi outside of the plant rhizosphere associated with an endangered Australian orchid
inferred← citeshttps://doi.org/10.1016/j.landurbplan.2022.104360openalex-snapshot
City life of mycorrhizal and wood-inhabiting macrofungi: Importance of urban areas for maintaining fungal biodiversity
inferred← citeshttps://doi.org/10.1016/j.myc.2020.05.003openalex-snapshot
Physisporinus is an important mycorrhizal partner for mycoheterotrophic plants: Identification of mycorrhizal fungi of three Yoania species
inferred← citeshttps://doi.org/10.1017/s0960258520000367openalex-snapshot
‘Dust seeds’ with undifferentiated embryos and their germination in mycoheterotrophic Monotropoideae (Ericaceae)
inferred← citeshttps://doi.org/10.1080/00275514.2022.2050127openalex-snapshot
Taxonomy and ecology of Physisporinus forming synnema-like structures in freshwater environments
inferred← citeshttps://doi.org/10.1080/15592324.2020.1785667openalex-snapshot
Use of radiocarbon for assessing the mycorrhizal status of mycoheterotrophic plants
inferred← citeshttps://doi.org/10.1093/aob/mcab003openalex-snapshot
Partial mycoheterotrophy is common among chlorophyllous plants with Paris-type arbuscular mycorrhiza
inferred← citeshttps://doi.org/10.1093/aob/mcab134openalex-snapshot
The Waiting Room Hypothesis revisited by orchids: were orchid mycorrhizal fungi recruited among root endophytes?
inferred← citeshttps://doi.org/10.1093/aob/mcae097openalex-snapshot
Mode of carbon gain and fungal associations of Neuwiedia malipoensis within the evolutionarily early-diverging orchid subfamily Apostasioideae
inferred← citeshttps://doi.org/10.1093/aob/mcv142openalex-snapshot
Orchid conservation: making the links
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/mcw147openalex-snapshot
Orchid conservation: further links
inferred← citeshttps://doi.org/10.1093/aobpla/plac021openalex-snapshot
Fungal association and root morphology shift stepwise during ontogenesis of orchidCremastra appendiculatatowards autotrophic nutrition
inferred← citeshttps://doi.org/10.1093/jxb/erac124openalex-snapshot
Foliar chlorophyll concentration modulates the degree of fungal exploitation in a rhizoctonia-associated orchid
inferred← citeshttps://doi.org/10.1093/sysbio/syaf069openalex-snapshot
Nuclear Phylogenomic Insights into Relationships, Support, and Conflict Among the Early Diverging Lineages of the Megadiverse Epidendroid Orchids
inferred← citeshttps://doi.org/10.1098/rsos.160427openalex-snapshot
The carbon and nitrogen ecophysiologies of two endemic tropical orchids mirrors those of their temperate relatives and the local environment
inferred← citeshttps://doi.org/10.1101/2022.12.16.519622openalex-snapshot
Root-associated Fungi in Orchidaceae: Diversity, Phylogeny, Ecology, and Outstanding Questions
inferred← citeshttps://doi.org/10.1111/1365-2435.13864openalex-snapshot
Subterranean morphology modulates the degree of mycoheterotrophy in a green orchid Calypso bulbosa exploiting wood‐decaying fungi
inferred← citeshttps://doi.org/10.1111/1365-2745.12831openalex-snapshot
Exploiting mycorrhizas in broad daylight: Partial mycoheterotrophy is a common nutritional strategy in meadow orchids
inferred← citeshttps://doi.org/10.1111/1365-2745.13165openalex-snapshot
Mycorrhizal symbioses and the evolution of trophic modes in plants
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/10.1111/1365-2745.70021openalex-snapshot
Global mycorrhizal status drives leaf δ 15 N patterns
inferred← citeshttps://doi.org/10.1111/geb.12920openalex-snapshot
Global distribution patterns of mycoheterotrophy
inferred← citeshttps://doi.org/10.1111/mec.14021openalex-snapshot
Comparison of green and albino individuals of the partially mycoheterotrophic orchid Epipactis helleborine on molecular identities of mycorrhizal fungi, nutritional modes and gene expression in mycorrhizal roots
inferred← citeshttps://doi.org/10.1111/mec.14524openalex-snapshot
The giant mycoheterotrophic orchid Erythrorchis altissima is associated mainly with a divergent set of wood‐decaying fungi
inferred← citeshttps://doi.org/10.1111/mec.15213openalex-snapshot
Comparative study of nutritional mode and mycorrhizal fungi in green and albino variants of Goodyera velutina, an orchid mainly utilizing saprotrophic rhizoctonia
inferred← citeshttps://doi.org/10.1111/nph.14551openalex-snapshot
Growing evidence for facultative biotrophy in saprotrophic fungi: data from microcosm tests with 201 species of wood‐decay basidiomycetes
inferred← citeshttps://doi.org/10.1111/nph.14895openalex-snapshot
Host preference and network properties in biotrophic plant–fungal associations
inferred← citeshttps://doi.org/10.1111/nph.15223openalex-snapshot
Mycorrhizal fungi affect orchid distribution and population dynamics
inferred← citeshttps://doi.org/10.1111/nph.16367openalex-snapshot
Discreet heterotrophs: green plants that receive fungal carbon through Paris‐type arbuscular mycorrhiza
inferred← citeshttps://doi.org/10.1111/nph.16409openalex-snapshot
Some mycoheterotrophic orchids depend on carbon from dead wood: novel evidence from a radiocarbon approach
inferred← citeshttps://doi.org/10.1111/nph.17049openalex-snapshot
Evidence for mycorrhizal cheating in Apostasia nipponica, an early‐diverging member of the Orchidaceae
inferred← citeshttps://doi.org/10.1111/nph.17313openalex-snapshot
Novel mycorrhizal cheating in a green orchid: Cremastraappendiculata depends on carbon from deadwood through fungal associations
inferred← citeshttps://doi.org/10.1111/nph.17523openalex-snapshot
Stigmatodactylus sikokianus (Orchidaceae) mainly acquires carbon from decaying litter through association with a specific clade of Serendipitaceae
inferred← citeshttps://doi.org/10.1111/nph.18991openalex-snapshot
Novel insights into orchid mycorrhiza functioning from stable isotope signatures of fungal pelotons
inferred← citeshttps://doi.org/10.1111/nph.71411openalex-snapshot
Partial mycoheterotrophy: a common strategy in arbuscular mycorrhizal plants?
inferred← citeshttps://doi.org/10.1111/pce.15167openalex-snapshot
Stable Isotope Signatures Illuminate Diverse Nutritional Strategies in Rhizoctonias and Their Orchid Partners
inferred← citeshttps://doi.org/10.1111/plb.70004openalex-snapshot
Partial mycoheterotrophy in Apostasia wallichii , an early‐diverging Asian tropical orchid
inferred← citeshttps://doi.org/10.1111/plb.70014openalex-snapshot
Green, variegated, and albino Cremastra variabilis provide insight into mycoheterotrophic evolution associated with wood‐decaying fungi
inferred← citeshttps://doi.org/10.1111/plb.70103openalex-snapshot
Mycorhizomes and ectomycorrhizal associations facilitate a mycoheterotrophic nutritional mode in the green orchid Cymbidium kanran
inferred← citeshttps://doi.org/10.1111/plb.70195openalex-snapshot
Mycorrhizal specificity of fully mycoheterotrophic Yoania in Taiwan and China and novel natural abundance stable isotope patterns
inferred← citeshttps://doi.org/10.1111/tpj.70045openalex-snapshot
Subterranean morphology underpins the degree of mycoheterotrophy, mycorrhizal associations, and plant vigor in a green orchid Oreorchis patens
inferred← citeshttps://doi.org/10.1139/cjb-2022-0052openalex-snapshot
Spatial separation of mycobionts in the giant, differentiated root system of Cyrtosia septentrionalis, a fully myco-heterotrophic orchid
inferred← citeshttps://doi.org/10.1186/s12866-020-01906-4openalex-snapshot
Molecular evidence supports simultaneous association of the achlorophyllous orchid Chamaegastrodia inverta with ectomycorrhizal Ceratobasidiaceae and Russulaceae
inferred← citeshttps://doi.org/10.1186/s40529-016-0137-7openalex-snapshot
Embryology of two mycoheterotrophic orchid species, Gastrodia elata and Gastrodia nantoensis: ovule and embryo development
inferred← citeshttps://doi.org/10.1186/s40529-017-0213-7openalex-snapshot
Post genomics era for orchid research
inferred← citeshttps://doi.org/10.1186/s40529-019-0280-zopenalex-snapshot
Ultrastructural changes during the symbiotic seed germination of Gastrodia elata with fungi, with emphasis on the fungal colonization region
inferred← citeshttps://doi.org/10.3389/fmicb.2020.574146openalex-snapshot
Successional Change of the Fungal Microbiome Pine Seedling Roots Inoculated With Tricholoma matsutake
inferred← citeshttps://doi.org/10.3389/fpls.2021.646325openalex-snapshot
Progress and Prospects of Mycorrhizal Fungal Diversity in Orchids
inferred← citeshttps://doi.org/10.3389/fpls.2021.775290openalex-snapshot
Mycorrhizal Switching and the Role of Fungal Abundance in Seed Germination in a Fully Mycoheterotrophic Orchid, Gastrodia confusoides
inferred← citeshttps://doi.org/10.3390/microorganisms7120586openalex-snapshot
Root-Associated Fungal Communities in Two Populations of the Fully Mycoheterotrophic Plant Arachnitis uniflora Phil. (Corsiaceae) in Southern Chile
inferred← citeshttps://doi.org/10.3732/ajb.1600334openalex-snapshot
Symbiont abundance can affect host plant population dynamics
inferred← citeshttps://doi.org/10.47371/mycosci.2025.07.005openalex-snapshot
Five Mycena species that induce seed germination in the mycoheterotrophic orchid Gastrodia
inferred← citeshttps://doi.org/10.69721/tps.j.2025.17.2.06openalex-snapshot
Relative gene expression of calcium binding protein in Dendrobium bigibbum Lindl. symbiotically grown with basidiomycetes
inferred← citeshttps://doi.org/10.70675/15f32752za04dz46adz8598z70a702c527faopenalex-snapshot
Symbioses mycorhiziennes des orchidées épiphytes
inferred← citeshttps://doi.org/10.70675/a464237azb310z49edz8c8dz7c504d1cc77fopenalex-snapshot
Evolution des interactions mycorhiziennes et de la mycohétérotrophie chez les orchidées
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