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The Waiting Room Hypothesis revisited by orchids: were orchid mycorrhizal fungi recruited among root endophytes?
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/9781118951446.ch5openalex-snapshot
Structure and development of orchid mycorrhizas
inferredcites →https://doi.org/10.1002/ajb2.1183openalex-snapshot
Stable isotope analyses reveal previously unknown trophic mode diversity in the Hymenochaetales
inferredcites →https://doi.org/10.1002/ppp3.10171openalex-snapshot
Vanilla aerial and terrestrial roots host rich communities of orchid mycorrhizal and ectomycorrhizal fungi
inferredcites →https://doi.org/10.1007/3-540-33526-9_9openalex-snapshot
Microbial Endophytes of Orchid Roots
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/s00248-003-2034-3openalex-snapshot
Chlorophyllous and Achlorophyllous Specimens of Epipactis microphylla (Neottieae, Orchidaceae) Are Associated with Ectomycorrhizal Septomycetes, including Truffles
inferredcites →https://doi.org/10.1007/s00572-008-0181-6openalex-snapshot
Mycorrhizal status and diversity of fungal endophytes in roots of common buckwheat (Fagopyrum esculentum) and tartary buckwheat (F. tataricum)
inferredcites →https://doi.org/10.1007/s00572-010-0307-5openalex-snapshot
Mycorrhizal specificity, preference, and plasticity of six slipper orchids from South Western China
inferredcites →https://doi.org/10.1007/s00572-013-0510-2openalex-snapshot
Symbiotic seed germination and protocorm development of Aa achalensis Schltr., a terrestrial orchid endemic from Argentina
inferredcites →https://doi.org/10.1007/s00572-013-0512-0openalex-snapshot
Endophytic and mycorrhizal fungi associated with roots of endangered native orchids from the Atlantic Forest, Brazil
inferredcites →https://doi.org/10.1007/s00572-014-0612-5openalex-snapshot
Mycorrhizal fungal diversity and community composition in a lithophytic and epiphytic orchid
inferredcites →https://doi.org/10.1007/s00572-016-0750-zopenalex-snapshot
Transfer to forest nurseries significantly affects mycorrhizal community composition of Asteropeia mcphersonii wildings
inferredcites →https://doi.org/10.1007/s00572-017-0774-zopenalex-snapshot
An annotated translation of Noël Bernard’s 1899 article ‘On the germination of Neottia nidus-avis’
inferredcites →https://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
inferredcites →https://doi.org/10.1007/s00572-019-00907-0openalex-snapshot
Are fungi from adult orchid roots the best symbionts at germination? A case study
inferredcites →https://doi.org/10.1007/s00572-020-00932-4openalex-snapshot
Three-year pot culture of Epipactis helleborine reveals autotrophic survival, without mycorrhizal networks, in a mixotrophic species
inferredcites →https://doi.org/10.1007/s00572-020-00993-5openalex-snapshot
Host population size is linked to orchid mycorrhizal fungal communities in roots and soil, which are shaped by microenvironment
inferredcites →https://doi.org/10.1007/s00572-020-01000-7openalex-snapshot
Serendipita restingae sp. nov. (Sebacinales): an orchid mycorrhizal agaricomycete with wide host range
inferredcites →https://doi.org/10.1007/s00572-021-01032-7openalex-snapshot
Partial and full mycoheterotrophy in green and albino phenotypes of the slipper orchid Cypripedium debile
inferredcites →https://doi.org/10.1007/s10265-013-0552-8openalex-snapshot
The rare terrestrial orchid Nervilia nipponica consistently associates with a single group of novel mycobionts
inferredcites →https://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
inferredcites →https://doi.org/10.1007/s10267-007-0360-xopenalex-snapshot
Pterostylis nutans (Orchidaceae) has a specific association with two Ceratobasidium root-associated fungi across its range in eastern Australia
inferredcites →https://doi.org/10.1007/s11557-006-0502-0openalex-snapshot
The simple-septate basidiomycetes: a synopsis
inferredcites →https://doi.org/10.1007/s11557-011-0754-1openalex-snapshot
Mycena sp., a mycorrhizal fungus of the orchid Dendrobium officinale
inferredcites →https://doi.org/10.1007/s11557-013-0936-0openalex-snapshot
Taxonomic re-evaluation of the Ceratobasidium-Rhizoctonia complex and Rhizoctonia butinii, a new species attacking spruce
inferredcites →https://doi.org/10.1007/s11557-019-01519-wopenalex-snapshot
Are Trechisporales ectomycorrhizal or non-mycorrhizal root endophytes?
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/bs.abr.2017.06.004openalex-snapshot
Plastid Complexity in Dinoflagellates: A Picture of Gains, Losses, Replacements and Revisions
inferredcites →https://doi.org/10.1016/j.fbr.2013.09.001openalex-snapshot
Lineages of ectomycorrhizal fungi revisited: Foraging strategies and novel lineages revealed by sequences from belowground
inferredcites →https://doi.org/10.1016/j.funeco.2013.03.004openalex-snapshot
Evolution of nutritional modes of Ceratobasidiaceae (Cantharellales, Basidiomycota) as revealed from publicly available ITS sequences
inferredcites →https://doi.org/10.1016/j.funeco.2017.10.004openalex-snapshot
Is Tuber melanosporum colonizing the roots of herbaceous, non-ectomycorrhizal plants?
inferredcites →https://doi.org/10.1016/j.funeco.2018.10.003openalex-snapshot
Molecular identifications uncover diverse fungal symbionts of Pleione (Orchidaceae)
inferredcites →https://doi.org/10.1016/j.funeco.2021.101071openalex-snapshot
Can orchid mycorrhizal fungi be persistently harbored by the plant host?
inferredcites →https://doi.org/10.1016/j.gecco.2016.03.011openalex-snapshot
Seasonal dynamics of mycorrhizal fungi in Paphiopedilum spicerianum (Rchb. f) Pfitzer — A critically endangered orchid from China
inferredcites →https://doi.org/10.1016/j.mycres.2009.05.002openalex-snapshot
Fungi from the roots of the common terrestrial orchid Gymnadenia conopsea
inferredcites →https://doi.org/10.1016/j.mycres.2009.07.004openalex-snapshot
Do Sebacinales commonly associate with plant roots as endophytes?
inferredcites →https://doi.org/10.1016/j.scitotenv.2021.146692openalex-snapshot
Partial overlap of fungal communities associated with nettle and poplar roots when co-occurring at a trace metal contaminated site
inferredcites →https://doi.org/10.1016/j.tplants.2008.11.004openalex-snapshot
Green plants that feed on fungi: facts and questions about mixotrophy
inferredcites →https://doi.org/10.1016/j.tplants.2014.09.005openalex-snapshot
Do chlorophyllous orchids heterotrophically use mycorrhizal fungal carbon?
inferredcites →https://doi.org/10.1016/j.ympev.2004.05.015openalex-snapshot
Molecular identification of mycorrhizal fungi in Neuwiedia veratrifolia (Orchidaceae)
inferredcites →https://doi.org/10.1016/s0953-7562(09)80984-2openalex-snapshot
Septal ultrastructure of some fungal endophytes from boreal orchid mycorrhizas
inferredcites →https://doi.org/10.1038/nature07891openalex-snapshot
Deep homology and the origins of evolutionary novelty
inferredcites →https://doi.org/10.1038/ng.3223openalex-snapshot
Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists
inferredcites →https://doi.org/10.1038/s41467-020-18795-wopenalex-snapshot
Large-scale genome sequencing of mycorrhizal fungi provides insights into the early evolution of symbiotic traits
inferredcites →https://doi.org/10.1038/srep37182openalex-snapshot
Habitat-driven variation in mycorrhizal communities in the terrestrial orchid genus Dactylorhiza
inferredcites →https://doi.org/10.1046/j.0962-1083.2001.01324.xopenalex-snapshot
Identification of mycorrhizal fungi from single pelotons of Dactylorhiza majalis (Orchidaceae) using single‐strand conformation polymorphism and mitochondrial ribosomal large subunit DNA sequences
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/10.1073/pnas.1710455114openalex-snapshot
Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
inferredcites →https://doi.org/10.1080/21655979.2019.1644854openalex-snapshot
RETRACTED ARTICLE: A comprehensive review on fungal endophytes and its dynamics on Orchidaceae plants: Current research, challenges and future possibilities
inferredcites →https://doi.org/10.1086/657955openalex-snapshot
The Effects of Above- and Belowground Mutualisms on Orchid Speciation and Coexistence
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/aob/mcv085openalex-snapshot
The importance of associations with saprotrophic non-Rhizoctoniafungi among fully mycoheterotrophic orchids is currently under-estimated: novel evidence from sub-tropical Asia
inferredcites →https://doi.org/10.1093/aob/mcw015openalex-snapshot
Differences in mycorrhizal communities betweenEpipactis palustris,E. helleborineand its presumed sister speciesE. neerlandica
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.2009.1884openalex-snapshot
Atractiellomycetes belonging to the ‘rust’ lineage (Pucciniomycotina) form mycorrhizae with terrestrial and epiphytic neotropical orchids
inferredcites →https://doi.org/10.1098/rspb.2015.1553openalex-snapshot
Orchid phylogenomics and multiple drivers of their extraordinary diversification
inferredcites →https://doi.org/10.1111/1365-2435.13042openalex-snapshot
Stable isotope signatures of underground seedlings reveal the organic matter gained by adult orchids from mycorrhizal fungi
inferredcites →https://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
inferredcites →https://doi.org/10.1111/1365-2745.12145openalex-snapshot
Critical importance of large native trees for conservation of a rare Neotropical epiphyte
inferredcites →https://doi.org/10.1111/1365-2745.12831openalex-snapshot
Exploiting mycorrhizas in broad daylight: Partial mycoheterotrophy is a common nutritional strategy in meadow orchids
inferredcites →https://doi.org/10.1111/1365-2745.13165openalex-snapshot
Mycorrhizal symbioses and the evolution of trophic modes in plants
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02424.xopenalex-snapshot
High specificity generally characterizes mycorrhizal association in rare lady's slipper orchids, genus Cypripedium
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04693.xopenalex-snapshot
Evolution of host breadth in broad interactions: mycorrhizal specificity in East Asian and North American rattlesnake plantains (Goodyera spp.) and their fungal hosts
inferredcites →https://doi.org/10.1111/j.1365-294x.2010.04785.xopenalex-snapshot
Low specificity and nested subset structure characterize mycorrhizal associations in five closely related species of the genus Orchis
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05692.xopenalex-snapshot
The role of epiphytism in architecture and evolutionary constraint within mycorrhizal networks of tropical orchids
inferredcites →https://doi.org/10.1111/j.1469-8137.2004.01114.xopenalex-snapshot
Mycorrhizal diversity in photosynthetic terrestrial orchids
inferredcites →https://doi.org/10.1111/j.1469-8137.2005.01364.xopenalex-snapshot
Mixotrophy in orchids: insights from a comparative study of green individuals and nonphotosynthetic individuals of Cephalanthera damasonium
inferredcites →https://doi.org/10.1111/j.1469-8137.2007.02064.xopenalex-snapshot
Sebacinales are common mycorrhizal associates of Ericaceae
inferredcites →https://doi.org/10.1111/j.1469-8137.2009.02773.xopenalex-snapshot
Fungal endophytes: diversity and functional roles
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.1469-8137.2010.03611.xopenalex-snapshot
A meta‐analysis of plant responses to dark septate root endophytes
inferredcites →https://doi.org/10.1111/j.1469-8137.2011.03796.xopenalex-snapshot
Analysis of network architecture reveals phylogenetic constraints on mycorrhizal specificity in the genus Orchis (Orchidaceae)
inferredcites →https://doi.org/10.1111/j.1558-5646.2007.00112.xopenalex-snapshot
THE EVOLUTIONARY HISTORY OF MYCORRHIZAL SPECIFICITY AMONG LADY'S SLIPPER ORCHIDS
inferredcites →https://doi.org/10.1111/jbi.13548openalex-snapshot
Latitudinal variation in mycorrhizal diversity associated with a European orchid
inferredcites →https://doi.org/10.1111/mec.14014openalex-snapshot
Mycorrhizal specificity does not limit the distribution of an endangered orchid species
inferredcites →https://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
inferredcites →https://doi.org/10.1111/nph.12348openalex-snapshot
Ploidy‐specific symbiotic interactions: divergence of mycorrhizal fungi between cytotypes of the G ymnadenia conopseagroup ( O rchidaceae)
inferredcites →https://doi.org/10.1111/nph.12640openalex-snapshot
Coexisting orchid species have distinct mycorrhizal communities and display strong spatial segregation
inferredcites →https://doi.org/10.1111/nph.13109openalex-snapshot
Temporal variation in mycorrhizal diversity and carbon and nitrogen stable isotope abundance in the wintergreen meadow orchid Anacamptis morio
inferredcites →https://doi.org/10.1111/nph.13288openalex-snapshot
Mycorrhizal ecology and evolution: the past, the present, and the future
inferredcites →https://doi.org/10.1111/nph.13977openalex-snapshot
Sebacinales – one thousand and one interactions with land plants
inferredcites →https://doi.org/10.1111/nph.14286openalex-snapshot
Fine‐scale spatial distribution of orchid mycorrhizal fungi in the soil of host‐rich grasslands
inferredcites →https://doi.org/10.1111/nph.14983openalex-snapshot
Time to re‐think fungal ecology? Fungal ecological niches are often prejudged
inferredcites →https://doi.org/10.1111/nph.15076openalex-snapshot
The origin and evolution of mycorrhizal symbioses: from palaeomycology to phylogenomics
inferredcites →https://doi.org/10.1111/nph.16321openalex-snapshot
Two ectomycorrhizal truffles, Tuber melanosporum and T. aestivum, endophytically colonise roots of non‐ectomycorrhizal plants in natural environments
inferredcites →https://doi.org/10.1111/nph.16409openalex-snapshot
Some mycoheterotrophic orchids depend on carbon from dead wood: novel evidence from a radiocarbon approach
inferredcites →https://doi.org/10.1111/nph.16545openalex-snapshot
In vitro evidence of root colonization suggests ecological versatility in the genus Mycena
inferredcites →https://doi.org/10.1111/nph.16604openalex-snapshot
Altered rhizoctonia assemblages in grasslands on ex‐arable land support germination of mycorrhizal generalist, not specialist orchids
inferredcites →https://doi.org/10.1111/nph.16637openalex-snapshot
The radiocarbon age of mycoheterotrophic plants
inferredcites →https://doi.org/10.1111/nph.17049openalex-snapshot
Evidence for mycorrhizal cheating in Apostasia nipponica, an early‐diverging member of the Orchidaceae
inferredcites →https://doi.org/10.1111/nph.17313openalex-snapshot
Novel mycorrhizal cheating in a green orchid: Cremastraappendiculata depends on carbon from deadwood through fungal associations
inferredcites →https://doi.org/10.1111/nph.17414openalex-snapshot
Symbiont switching and trophic mode shifts in Orchidaceae
inferredcites →https://doi.org/10.1111/nph.17459openalex-snapshot
A fine‐scale spatial analysis of fungal communities on tropical tree bark unveils the epiphytic rhizosphere in orchids
inferredcites →https://doi.org/10.1111/nph.17523openalex-snapshot
Stigmatodactylus sikokianus (Orchidaceae) mainly acquires carbon from decaying litter through association with a specific clade of Serendipitaceae
inferredcites →https://doi.org/10.1126/science.1221748openalex-snapshot
The Paleozoic Origin of Enzymatic Lignin Decomposition Reconstructed from 31 Fungal Genomes
inferredcites →https://doi.org/10.1128/aem.01911-09openalex-snapshot
Identity, Diversity, and Molecular Phylogeny of the Endophytic Mycobiota in the Roots of Rare Wild Rice ( Oryza granulate ) from a Nature Reserve in Yunnan, China
inferredcites →https://doi.org/10.1139/b06-101openalex-snapshot
Cephalanthera longifolia (Neottieae, Orchidaceae) is mixotrophic: a comparative study between green and nonphotosynthetic individuals
inferredcites →https://doi.org/10.1139/cjb-2013-0079openalex-snapshot
Geography and soil chemistry drive the distribution of fungal associations in lady’s slipper orchid,Cypripedium acaule
inferredcites →https://doi.org/10.1186/1741-7007-7-13openalex-snapshot
The relative ages of ectomycorrhizal mushrooms and their plant hosts estimated using Bayesian relaxed molecular clock analyses
inferredcites →https://doi.org/10.1371/journal.pone.0016793openalex-snapshot
Sebacinales Everywhere: Previously Overlooked Ubiquitous Fungal Endophytes
inferredcites →https://doi.org/10.1371/journal.pone.0164108openalex-snapshot
Mycorrhizal Fungal Diversity and Community Composition in Two Closely Related Platanthera (Orchidaceae) Species
inferredcites →https://doi.org/10.1371/journal.ppat.1002290openalex-snapshot
Endophytic Life Strategies Decoded by Genome and Transcriptome Analyses of the Mutualistic Root Symbiont Piriformospora indica
inferredcites →https://doi.org/10.17581/bp.2018.07106openalex-snapshot
A mixotrophy is in question: new data on fungal community associated with photosynthetic terrestrial orchid Goodyera repens
inferredcites →https://doi.org/10.2307/3545919openalex-snapshot
Endophyte: The Evolution of a Term, and Clarification of Its Use and Definition
inferredcites →https://doi.org/10.2307/3761116openalex-snapshot
Mycena anoectochila sp. nov. Isolated from Mycorrhizal Roots of Anoectochilus roxburghii from Xishuangbanna, China
inferredcites →https://doi.org/10.30848/pjb2020-2(42)openalex-snapshot
Mycorrhizal fungi of some Orchis species of Turkey
inferredcites →https://doi.org/10.3389/fmicb.2016.00332openalex-snapshot
Piriformospora indica: Potential and Significance in Plant Stress Tolerance
inferredcites →https://doi.org/10.3389/fpls.2017.01497openalex-snapshot
Mycorrhizal Associations and Trophic Modes in Coexisting Orchids: An Ecological Continuum between Auto- and Mixotrophy
inferredcites →https://doi.org/10.3389/fpls.2021.618140openalex-snapshot
Mycorrhizal Communities and Isotope Signatures in Two Partially Mycoheterotrophic Orchids
inferredcites →https://doi.org/10.3389/fpls.2021.646325openalex-snapshot
Progress and Prospects of Mycorrhizal Fungal Diversity in Orchids
inferredcites →https://doi.org/10.3390/plants10010018openalex-snapshot
Temporal Variation in Community Composition of Root Associated Endophytic Fungi and Carbon and Nitrogen Stable Isotope Abundance in Two Bletilla Species (Orchidaceae)
inferredcites →https://doi.org/10.3732/ajb.0900101openalex-snapshot
Mycorrhizal diversity in Apostasia (Orchidaceae) indicates the origin and evolution of orchid mycorrhiza
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.1000486openalex-snapshot
Photosynthetic Mediterranean meadow orchids feature partial mycoheterotrophy and specific mycorrhizal associations
inferredcites →https://doi.org/10.3732/ajb.1100464openalex-snapshot
Shifts in mycorrhizal fungi during the evolution of autotrophy to mycoheterotrophy in Cymbidium (Orchidaceae)
inferredcites →https://doi.org/10.3732/ajb.1600127openalex-snapshot
Age‐dependent mycorrhizal specificity in an invasive orchid, Oeceoclades maculata
inferredcites →https://doi.org/10.3767/003158515x688433openalex-snapshot
Fungal Planet description sheets: 320–370
inferredcites →https://doi.org/10.4161/psb.5.4.10791openalex-snapshot
Saprotrophic fungal symbionts in tropical achlorophyllous orchids
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.3897/imafungus.16.143240zenodo-depositor-declared
A fusarioid fungus forms mutualistic interactions with poplar trees that resemble ectomycorrhizal symbiosis
inferred← citeshttps://doi.org/10.1002/ajb2.70054openalex-snapshot
A phylogenetic study of the Cantharellales supports recognition of four families and independent gains of biotrophic nutritional modes
inferred← citeshttps://doi.org/10.1002/ece3.10863openalex-snapshot
Co‐occurring orchid species associated with different low‐abundance mycorrhizal fungi from the soil in a high‐diversity conservation area in Denmark
inferred← citeshttps://doi.org/10.1002/ece3.73805openalex-snapshot
Broad Fungal Compatibility and Seed Size May Facilitate Invasiveness in Two Asian Terrestrial Orchids Spathoglottis plicata and Arundina graminifolia
inferred← citeshttps://doi.org/10.1002/jobm.70164openalex-snapshot
Coprinellus sp. DJL‐31 Promotes Both Seed Germination and Pseudobulb Growth in Cremastra appendiculata
inferred← citeshttps://doi.org/10.1002/pei3.10146openalex-snapshot
Diversity of unique, nonmycorrhizal endophytic fungi in cultivated Phalaenopsis orchids: A pilot study
inferred← citeshttps://doi.org/10.1002/pei3.70096openalex-snapshot
Habitat Disturbance Promotes Shifts in the Abundance of Major Fungal Phyla in the Roots of a Native Orchid, Tipularia discolor
inferred← citeshttps://doi.org/10.1002/ppp3.10476openalex-snapshot
Mycorrhizal communities of Vanilla planifolia in an introduction area (La Réunion) under varying cultivation practices
inferred← citeshttps://doi.org/10.1007/978-1-0716-4031-9_13openalex-snapshot
Transcriptomics Analysis in the Study of Mycorrhizal Symbiosis in Orchids
inferred← citeshttps://doi.org/10.1007/978-981-99-1079-3_8openalex-snapshot
Asymbiotic Seed Germination in Terrestrial Orchids: Problems, Progress, and Prospects
inferred← citeshttps://doi.org/10.1007/s00248-026-02830-2openalex-snapshot
Multiscale Structuring of Mycorrhizal Fungal Communities of Tropical Epiphytic Orchids
inferred← citeshttps://doi.org/10.1007/s00572-022-01095-0openalex-snapshot
Mycorrhizal diversity and community composition in co-occurring Cypripedium species
inferred← citeshttps://doi.org/10.1007/s00572-024-01138-8openalex-snapshot
Mycobiont identity and light conditions affect belowground morphology and physiology of a mixotrophic orchid Cremastra variabilis (Orchidaceae)
inferred← citeshttps://doi.org/10.1007/s00572-024-01141-zopenalex-snapshot
Mycorrhizas in South American Ericaceae
inferred← citeshttps://doi.org/10.1007/s00572-024-01171-7openalex-snapshot
Variations in the root mycobiome and mycorrhizal fungi between different types of Vanilla forest farms on Réunion Island
inferred← citeshttps://doi.org/10.1007/s00572-025-01184-wopenalex-snapshot
Unlocking germination: the role of mycorrhizal strain and seed provenance in driving seed germination of a widespread terrestrial orchid
inferred← citeshttps://doi.org/10.1007/s00572-025-01216-5openalex-snapshot
Ecological specificity of fungi on seedling establishment in Dendrobium huoshanense: a narrow distributed medicinal orchid
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/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/s11627-025-10544-2openalex-snapshot
Divergent in vitro responses to asymbiotic seed germination media in Ophrys reinholdii subsp. straussii and Comperia comperiana: the dual impact of species and media
inferred← citeshttps://doi.org/10.1007/s13199-024-00974-8openalex-snapshot
Improved use of mycorrhizal fungi for upscaling of orchid cultivation and population restoration of endangered orchids in China
inferred← citeshttps://doi.org/10.1007/s13199-026-01145-7openalex-snapshot
Trade-offs between competitive ability and host germination-inducing capacity in the orchid mycorrhizal genus Ceratobasidium with terrestrial orchids of the genus Bipinnula
inferred← citeshttps://doi.org/10.1007/s13199-026-01157-3openalex-snapshot
Diversity and dynamics of culturable fungi associated with the roots of the endemic and endangered orchid Rhynchostele cervantesii
inferred← citeshttps://doi.org/10.1007/s13199-026-01166-2openalex-snapshot
Mycorrhizal associations in pteridophytes: current perspectives and emerging research gaps
inferred← citeshttps://doi.org/10.1016/b978-0-323-91734-6.00004-1openalex-snapshot
Rhizoctonia spp. as beneficial and mycorrhizal fungi
inferred← citeshttps://doi.org/10.1016/b978-0-443-13318-3.00012-4openalex-snapshot
Endophytic fungi: perspectives for microbial engineering
inferred← citeshttps://doi.org/10.1016/j.chmed.2024.03.001openalex-snapshot
Perspective and challenges of mycorrhizal symbiosis in orchid medicinal plants
inferred← citeshttps://doi.org/10.1016/j.gecco.2023.e02778openalex-snapshot
Ancient tea gardens play important role on in situ conservation of epiphytic orchids in southwest Yunnan, China
inferred← citeshttps://doi.org/10.1016/j.jnc.2026.127364openalex-snapshot
Ecogeographical isolation and niche specialization inform subspecies-level conservation units in Vanilla pompona (Orchidaceae)
inferred← citeshttps://doi.org/10.1016/j.pbi.2022.102226openalex-snapshot
Determinants of endophytic and pathogenic lifestyle in root colonizing fungi
inferred← citeshttps://doi.org/10.1016/j.pbi.2024.102627openalex-snapshot
Different roles of the phytohormone gibberellin in the wide-spread arbuscular mycorrhiza and in orchid mycorrhiza
inferred← citeshttps://doi.org/10.1016/j.pedsph.2024.01.004openalex-snapshot
The necessity to expand mycorrhizal boundaries: Including the fungal endophytes that possess key mycorrhizal criteria
inferred← citeshttps://doi.org/10.1016/j.pld.2025.08.002openalex-snapshot
Mycorrhizal communities in Orchidaceae are likely shaped by plant trophic mode and biogeography but not phylogeny
inferred← citeshttps://doi.org/10.1016/j.rhisph.2024.101013openalex-snapshot
Diverging role of phytohormones and soil nutrients between two broad and narrow-distribution orchids of Satyrium species
inferred← citeshttps://doi.org/10.1016/j.rhisph.2025.101147openalex-snapshot
Insights into mycorrhizal fungal community composition in two Anacamptis species from Türkiye
inferred← citeshttps://doi.org/10.1038/s41598-026-56854-2openalex-snapshot
Eisosomal proteins are essential for plant–fungal interaction of Neurospora crassa and the sweetgrass Brachypodium distachyon
inferred← citeshttps://doi.org/10.1051/e3sconf/202344404009openalex-snapshot
Application of Biofertilizing Agents and Entomopathogenic Fungi in Lowland Rice
inferred← citeshttps://doi.org/10.1080/00275514.2026.2616180openalex-snapshot
Exploring the diversity of Peziza echinospora (Ascomycota, Pezizomycetes) and related species in Australia, with descriptions of the new species P. austroechinospora and P. meridionalis
inferred← citeshttps://doi.org/10.1080/00275514.2026.2707363openalex-snapshot
High ascomycete diversity and novel fungal associations found in expanding Epipactis helleborine populations outside their native range
inferred← citeshttps://doi.org/10.1080/15592324.2023.2180159openalex-snapshot
Effect of light conditions on trophic level and gene expression of partially mycoheterotrophic orchid, Cymbidium goeringii
inferred← citeshttps://doi.org/10.1080/19420889.2024.2439798openalex-snapshot
Extract from endophytic Fusarium isolates stimulates seed germination of the host and protocorm development of non-host orchids
inferred← citeshttps://doi.org/10.1080/21501203.2026.2646023openalex-snapshot
Mycorrhizal specificity in orchids: a multidimensional filtering framework
inferred← citeshttps://doi.org/10.1093/aob/mcae202openalex-snapshot
Orchid phylogenetics and evolution: history, current status and prospects
inferred← citeshttps://doi.org/10.1093/aob/mcaf100openalex-snapshot
Mycoheterotrophic continuum in rhizoctonia associations: genetic divergence and carbon acquisition variation among Odontochilus orchids
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/femsre/fuag035openalex-snapshot
Decoding dark septate endophyte symbiosis: a functional and ecological perspective
inferred← citeshttps://doi.org/10.1093/hr/uhac220openalex-snapshot
Advances and prospects of orchid research and industrialization
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/plphys/kiad198openalex-snapshot
Symbiosis between Dendrobium catenatum protocorms and Serendipita indica involves the plant hypoxia response pathway
inferred← citeshttps://doi.org/10.1093/plphys/kiad232openalex-snapshot
“Smother love” of mycorrhiza: hypoxic germination of orchids
inferred← citeshttps://doi.org/10.1093/plphys/kiad517openalex-snapshot
Autoactivation of mycorrhizal symbiosis signaling through gibberellin deactivation in orchid seed germination
inferred← citeshttps://doi.org/10.1093/sysbio/syae070openalex-snapshot
Discordance Down Under: Combining Phylogenomics and Fungal Symbioses to Detangle Difficult Nodes in a Diverse Tribe of Australian Terrestrial Orchids
inferred← citeshttps://doi.org/10.1098/rsos.251501openalex-snapshot
Growth and development of staghorn fern colonies ( Platycerium bifurcatum , Polypodiaceae)
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/10.1101/2025.01.08.631981openalex-snapshot
Breaking boundaries: fungi in the “rhizoctonia” species complex exhibit systemic colonization in three terrestrial orchid species
inferred← citeshttps://doi.org/10.1111/1365-2435.14354openalex-snapshot
Variation in mycorrhizal communities and the level of mycoheterotrophy in grassland and Forest populations of Neottia ovata (Orchidaceae)
inferred← citeshttps://doi.org/10.1111/1365-2435.14690openalex-snapshot
Mycorrhizal specialization toward each distinct Oliveonia fungus in two closely related photosynthetic Dactylostalix orchids
inferred← citeshttps://doi.org/10.1111/1365-2745.13986openalex-snapshot
Spatial turnover of fungi and partner choice shape mycorrhizal networks in epiphytic orchids
inferred← citeshttps://doi.org/10.1111/1365-2745.14086openalex-snapshot
Biological Flora of Britain and Ireland: Liparis loeselii
inferred← citeshttps://doi.org/10.1111/1442-1984.12369openalex-snapshot
Partial mycoheterotrophy in rhizoctonia‐associated orchid Cheirostylis liukiuensis
inferred← citeshttps://doi.org/10.1111/1442-1984.12432openalex-snapshot
The epiphytic orchid Vanda falcata is predominantly associated with a single Tulasnellaceae fungus in adulthood, and Ceratobasidiaceae fungi strongly induce its seed germination in vitro
inferred← citeshttps://doi.org/10.1111/jbi.15056openalex-snapshot
Orchid Mycorrhizal Communities Associated With Orchis italica Are Shaped by Ecological Factors and Geographical Gradients
inferred← citeshttps://doi.org/10.1111/jipb.70315openalex-snapshot
Orchid genome evolution and trait innovation
inferred← citeshttps://doi.org/10.1111/mec.16918openalex-snapshot
Orchid–mycorrhizal fungi interactions reveal a duality in their network structure in two European regions differing in climate
inferred← citeshttps://doi.org/10.1111/njb.04083openalex-snapshot
The role of mycorrhizal fungi in driving ecotype formation in mycoheterotrophic plants
inferred← citeshttps://doi.org/10.1111/nph.19385openalex-snapshot
Metabarcoding read abundances of orchid mycorrhizal fungi are correlated to copy numbers estimated using ddPCR
inferred← citeshttps://doi.org/10.1111/nph.19580openalex-snapshot
The origin and speciation of orchids
inferred← citeshttps://doi.org/10.1111/nph.20251openalex-snapshot
Origins of xyloglucan‐degrading enzymes in fungi
inferred← citeshttps://doi.org/10.1111/nph.70106openalex-snapshot
Mixotrophy in orchids: facts, questions, and perspectives
inferred← citeshttps://doi.org/10.1111/nph.70772openalex-snapshot
Endophytes with mycorrhizal potentials: biological and ecological implications
inferred← citeshttps://doi.org/10.1111/nph.71175openalex-snapshot
Endophytic and ectomycorrhizal, an overlooked dual ecological niche? Insights from natural environments and Russula species
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/pce.15612openalex-snapshot
Metabolic Shifts and Nutrient Transfer Patterns in Orchid Seeds During Symbiotic Germination
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.70269openalex-snapshot
Underground allies : Mycorrhizal flexibility facilitates orchid occurrence in post‐mining landscapes
inferred← citeshttps://doi.org/10.1128/spectrum.02573-25openalex-snapshot
Study on geographic differentiation and environment-host synergistic assembly mechanism of root-associated fungal communities in Paphiopedilum purpuratum
inferred← citeshttps://doi.org/10.1186/s12864-024-10143-2openalex-snapshot
The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.1186/s12864-026-12572-7openalex-snapshot
Comparison and structure of fungal diversity in roots and rhizosphere soils of wild and reintroduced populations of three Paphiopedilum species
inferred← citeshttps://doi.org/10.1186/s12870-022-03760-0openalex-snapshot
What role does the seed coat play during symbiotic seed germination in orchids: an experimental approach with Dendrobium officinale
inferred← citeshttps://doi.org/10.1186/s12870-022-04007-8openalex-snapshot
An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.1186/s12870-023-04436-zopenalex-snapshot
Stoichiometry of carbon, nitrogen and phosphorus is closely linked to trophic modes in orchids
inferred← citeshttps://doi.org/10.1186/s12870-024-05721-1openalex-snapshot
Japonolirion osense, a close relative of the mycoheterotrophic genus Petrosavia, exhibits complete autotrophic capabilities
inferred← citeshttps://doi.org/10.1186/s40793-022-00434-0openalex-snapshot
Structure and specialization of mycorrhizal networks in phylogenetically diverse tropical communities
inferred← citeshttps://doi.org/10.1186/s43008-024-00165-6openalex-snapshot
Integration of fungal transcriptomics and metabolomics provides insights into the early interaction between the ORM fungus Tulasnella sp. and the orchid Serapias vomeracea seeds
inferred← citeshttps://doi.org/10.15252/embr.202357455openalex-snapshot
Co‐evolution within the plant holobiont drives host performance
inferred← citeshttps://doi.org/10.1590/1677-941x-abb-2023-0196openalex-snapshot
Narrow mycorrhizae and large non-mycorrhizal fungal diversity associated with roots of Cattleya milleri, an endemic and endangered orchid from a rupestrian hotspot in the “Quadrilátero Ferrífero” of Minas Gerais - Brazil
inferred← citeshttps://doi.org/10.17129/botsci.3470openalex-snapshot
Allogamy, metaxenia and hybrids in orchids, what do we know about it?
inferred← citeshttps://doi.org/10.21070/2023/978-623-464-079-3openalex-snapshot
Pemanfaatan Fungi Agen Hayati Sebagai Mitigasi Cekaman Lingkungan Dalam Budidaya Padi dan Kedele
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2885848/v1openalex-snapshot
High endophytic diversity associated with roots of Cattleya milleri, an endemic orchid from rupestrian grasslands of the “Quadrilátero Ferrífero”, a Brazilian savanna hotspot area in Minas Gerais
inferred← citeshttps://doi.org/10.3389/fevo.2023.1057940openalex-snapshot
Diversity and specificity of orchid mycorrhizal fungi in a leafless epiphytic orchid, Dendrophylax lindenii and the potential role of fungi in shaping its fine-scale distribution
inferred← citeshttps://doi.org/10.3389/fmicb.2022.928967openalex-snapshot
Biosynthetic Mechanisms of Secondary Metabolites Promoted by the Interaction Between Endophytes and Plant Hosts
inferred← citeshttps://doi.org/10.3389/fmicb.2022.933017openalex-snapshot
Endophytes and their potential in biotic stress management and crop production
inferred← citeshttps://doi.org/10.3389/fmicb.2022.961172openalex-snapshot
Effects of a Dark Septate Fungal Endophyte on the Growth and Physiological Response of Seedlings to Drought in an Epiphytic Orchid
inferred← citeshttps://doi.org/10.3389/fmicb.2023.1233555openalex-snapshot
Effect of symbiotic fungi-Armillaria gallica on the yield of Gastrodia elata Bl. and insight into the response of soil microbial community
inferred← citeshttps://doi.org/10.3389/fmicb.2026.1752368openalex-snapshot
Biogeographic patterns, assembly processes, and functional potential of root-associated microbiomes across the native range of the endangered orchid Changnienia amoena
inferred← citeshttps://doi.org/10.3389/fpls.2022.823794openalex-snapshot
Compatible and Incompatible Mycorrhizal Fungi With Seeds of Dendrobium Species: The Colonization Process and Effects of Coculture on Germination and Seedling Development
inferred← citeshttps://doi.org/10.3389/fpls.2022.880600openalex-snapshot
Comparative Transcriptomics Analysis of the Symbiotic Germination of D. officinale (Orchidaceae) With Emphasis on Plant Cell Wall Modification and Cell Wall-Degrading Enzymes
inferred← citeshttps://doi.org/10.3389/fpls.2023.1114105openalex-snapshot
A novel method to produce massive seedlings via symbiotic seed germination in orchids
inferred← citeshttps://doi.org/10.3389/fpls.2024.1415401openalex-snapshot
Roles of mycorrhizal fungi on seed germination of two Chinese medicinal orchids: need or do not need a fungus?
inferred← citeshttps://doi.org/10.3390/d14060478openalex-snapshot
Root-Associated Endophytic and Mycorrhizal Fungi from the Epiphytic Orchid Maxillaria acuminata in a Tropical Montane Forest in Southern Ecuador
inferred← citeshttps://doi.org/10.3390/d18060359openalex-snapshot
Cultivation Mode Reshapes Root Fungal Endophyte Communities in Dendrobium officinale (Orchidaceae)
inferred← citeshttps://doi.org/10.3390/jof8101036openalex-snapshot
Using Ex Situ Seedling Baiting to Capture Seedling-Associated Mycorrhizal Fungi in Medicinal Orchid Dendrobium officinale
inferred← citeshttps://doi.org/10.3390/microorganisms12061054openalex-snapshot
Coriolopsis strumosa as an Orchid Endophytic Fungus and Its Spatial Distribution in Epidendrum sp. (Orchidaceae)
inferred← citeshttps://doi.org/10.3390/microorganisms13102229openalex-snapshot
Isolation of Endophytic Phosphate-Solubilizing Bacteria from Chinese Cymbidium (Cymbidium spp.) Orchid Roots
inferred← citeshttps://doi.org/10.3390/microorganisms14010174openalex-snapshot
Deciphering Molecular Pathways of Bletilla striata Seeds Symbiotic Germination with Tulasnella sp. bj1
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/10.48130/opr-0024-0027openalex-snapshot
Microbial community structure and diversity of endophytic and rhizosphere of Cypripedium species in Changbai Mountains
inferred← citeshttps://doi.org/10.5586/asbp/175378openalex-snapshot
The long-term survival and climatic distribution of mixotrophic and mycoheterotrophic orchids
inferred← citeshttps://doi.org/10.5772/intechopen.1008909openalex-snapshot
Fungi Associated with Other Organisms: Diversity, Interactions and Ecological Importance
inferred← citeshttps://doi.org/10.6084/m9.figshare.20347538openalex-snapshot
Additional file 1 of Structure and specialization of mycorrhizal networks in phylogenetically diverse tropical communities
inferred← citeshttps://doi.org/10.6084/m9.figshare.20407441openalex-snapshot
Additional file 1 of What role does the seed coat play during symbiotic seed germination in orchids: an experimental approach with Dendrobium officinale
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603520openalex-snapshot
Additional file 1 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603523openalex-snapshot
Additional file 2 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603526openalex-snapshot
Additional file 3 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603529openalex-snapshot
Additional file 4 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603532openalex-snapshot
Additional file 5 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603535openalex-snapshot
Additional file 6 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.22603538openalex-snapshot
Additional file 7 of An exploration of mechanism of high quality and yield of Gastrodia elata Bl. f. glauca by the isolation, identification and evaluation of Armillaria
inferred← citeshttps://doi.org/10.6084/m9.figshare.24130188openalex-snapshot
Additional file 1 of Stoichiometry of carbon, nitrogen and phosphorus is closely linked to trophic modes in orchids
inferred← citeshttps://doi.org/10.6084/m9.figshare.24130191openalex-snapshot
Additional file 2 of Stoichiometry of carbon, nitrogen and phosphorus is closely linked to trophic modes in orchids
inferred← citeshttps://doi.org/10.6084/m9.figshare.24130197openalex-snapshot
Additional file 3 of Stoichiometry of carbon, nitrogen and phosphorus is closely linked to trophic modes in orchids
inferred← citeshttps://doi.org/10.6084/m9.figshare.25309960openalex-snapshot
Additional file 1 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.25310262openalex-snapshot
Additional file 2 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686836openalex-snapshot
Additional file 3 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686839openalex-snapshot
Additional file 4 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686842openalex-snapshot
Additional file 5 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686845openalex-snapshot
Additional file 6 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686848openalex-snapshot
Additional file 7 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686851openalex-snapshot
Additional file 8 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686854openalex-snapshot
Additional file 9 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686857openalex-snapshot
Additional file 10 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686860openalex-snapshot
Additional file 11 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.6084/m9.figshare.26686863openalex-snapshot
Additional file 12 of The structure and diversity of bacteria and fungi in the roots and rhizosphere soil of three different species of Geodorum
inferred← citeshttps://doi.org/10.70675/15f32752za04dz46adz8598z70a702c527faopenalex-snapshot
Symbioses mycorhiziennes des orchidées épiphytes
inferred← citeshttps://doi.org/10.7287/peerj.13610v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Fungal diversity in shade-coffee plantations in Soconusco, Mexico (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13610v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Fungal diversity in shade-coffee plantations in Soconusco, Mexico (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.13610v0.2/reviews/2openalex-snapshot
Peer Review #2 of "Fungal diversity in shade-coffee plantations in Soconusco, Mexico (v0.2)"
inferred← citeshttps://doi.org/10.7717/peerj.13610openalex-snapshot
Fungal diversity in shade-coffee plantations in Soconusco, Mexico
inferred← citeshttps://doi.org/10.7717/peerj.21406openalex-snapshot
Mycorrhizal association impacts fitness of epiphytic orchids in situ
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