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High‐resolution secondary ion mass spectrometry analysis of carbon dynamics in mycorrhizas formed by an obligately myco‐heterotrophic orchid
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-1-4614-5209-6_8openalex-snapshot
The Physiological Ecology of Mycoheterotrophy
inferredcites →https://doi.org/10.1007/978-1-59745-294-6_8openalex-snapshot
Recent Advances in High-Pressure Freezing
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/10.1007/978-94-017-1284-2_15openalex-snapshot
Recent developments in the study of orchid mycorrhiza
inferredcites →https://doi.org/10.1007/s00216-011-5484-3openalex-snapshot
Elemental imaging at the nanoscale: NanoSIMS and complementary techniques for element localisation in plants
inferredcites →https://doi.org/10.1007/s00442-006-0581-2openalex-snapshot
Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae
inferredcites →https://doi.org/10.1016/b978-0-12-370526-6.x5001-6openalex-snapshot
Mycorrhizal Symbiosis
inferredcites →https://doi.org/10.1016/j.apsusc.2004.03.155openalex-snapshot
QSA influences on isotopic ratio measurements
inferredcites →https://doi.org/10.1016/j.mycres.2006.11.006openalex-snapshot
Diversity of mycorrhizal fungi of terrestrial orchids: compatibility webs, brief encounters, lasting relationships and alien invasions
inferredcites →https://doi.org/10.1016/j.mycres.2009.07.007openalex-snapshot
Identity and specificity of the fungi forming mycorrhizas with the rare mycoheterotrophic orchid Rhizanthella gardneri
inferredcites →https://doi.org/10.1016/s0022-5320(69)90033-1openalex-snapshot
A low-viscosity epoxy resin embedding medium for electron microscopy
inferredcites →https://doi.org/10.1023/a:1020246715436openalex-snapshot
Recent developments in the study of orchid mycorrhiza
inferredcites →https://doi.org/10.1038/41557openalex-snapshot
Net transfer of carbon between ectomycorrhizal tree species in the field
inferredcites →https://doi.org/10.1038/nature10745openalex-snapshot
Multi-isotope imaging mass spectrometry reveals slow protein turnover in hair-cell stereocilia
inferredcites →https://doi.org/10.1046/j.1469-8137.1999.00531-3.xopenalex-snapshot
Orchid biology: reviews and perspectives
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/10.1051/epjap:2001160openalex-snapshot
Precise in situ measurements of isotopic abundances with pulse counting of sputtered ions
inferredcites →https://doi.org/10.1063/1.4823194openalex-snapshot
Data Reduction and Error Analysis for the Physical Sciences
inferredcites →https://doi.org/10.1071/bt08031openalex-snapshot
Habitat characteristics of the rare underground orchid Rhizanthella gardneri
inferredcites →https://doi.org/10.1093/aob/mcm018openalex-snapshot
Mycorrhizal Acquisition of Inorganic Phosphorus by the Green-leaved Terrestrial Orchid Goodyera repens
inferredcites →https://doi.org/10.1093/molbev/msr028openalex-snapshot
Rampant Gene Loss in the Underground Orchid Rhizanthella gardneri Highlights Evolutionary Constraints on Plastid Genomes
inferredcites →https://doi.org/10.1111/j.1461-0248.2012.01830.xopenalex-snapshot
Ecological interactions drive evolutionary loss of traits
inferredcites →https://doi.org/10.1111/j.1469-8137.1967.tb06016.xopenalex-snapshot
CARBOHYDRATE TRANSLOCATION IN ORCHID MYCORRHIZAS
inferredcites →https://doi.org/10.1111/j.1469-8137.1971.tb02546.xopenalex-snapshot
ANALYSIS OF THE POST‐INFECTION GROWTH STIMULUS IN ORCHID MYCORRHIZA
inferredcites →https://doi.org/10.1111/j.1469-8137.1979.tb00733.xopenalex-snapshot
FAVOLASCHIA DYBOWSKYANA (SINGER) SINGER (APHYLLOPHORALES), A NEW ORCHID MYCORRHIZAL FUNGUS FROM TROPICAL AFRICA
inferredcites →https://doi.org/10.1111/j.1469-8137.1985.tb02871.xopenalex-snapshot
CARBON MOVEMENT BETWEEN HOST AND MYCORRHIZAL ENDOPHYTE DURING THE DEVELOPMENT OF THE ORCHID GOODYERA REPENS Br
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.1469-8137.2006.01767.xopenalex-snapshot
Mutualistic mycorrhiza in orchids: evidence from plant–fungus carbon and nitrogen transfers in the green‐leaved terrestrial orchid Goodyera repens
inferredcites →https://doi.org/10.1111/j.1469-8137.2008.02533.xopenalex-snapshot
Giving and receiving: measuring the carbon cost of mycorrhizas in the green orchid, Goodyera repens
inferredcites →https://doi.org/10.1111/j.1469-8137.2010.03246.xopenalex-snapshot
Carbon and nitrogen supply to the underground orchid, Rhizanthella gardneri
inferredcites →https://doi.org/10.1111/j.1600-0706.2008.17116.xopenalex-snapshot
Orchid mycorrhiza: implications of a mycophagous life style
inferredcites →https://doi.org/10.1139/b90-141openalex-snapshot
Synthesis of mycorrhizae between protocorms of Goodyera repens (Orchidaceae) and Ceratobasidium cereale
inferredcites →https://doi.org/10.1186/1741-7007-7-1openalex-snapshot
Microarray and cDNA sequence analysis of transcription during nerve-dependent limb regeneration
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/10.1890/11-2120.1openalex-snapshot
Why do mixotrophic plants stay green? A comparison between green and achlorophyllous orchid individuals in situ
inferredcites →https://doi.org/10.5860/choice.31-2679openalex-snapshot
Phylogeny and classification of the orchid family
inferredcites →https://doi.org/10.5860/choice.38-1564openalex-snapshot
Monocots: systematics and evolution
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4669665openalex-extracted
Coprinellus Radians Isolated from the Rhizome of Cremastra Appendiculata Effectively Promote Seed Germination and Seedling Development
inferred← citeshttps://doi.org/10.1002/9781118951446.ch5openalex-snapshot
Structure and development of orchid mycorrhizas
inferred← citeshttps://doi.org/10.1007/978-1-0716-1585-0_6openalex-snapshot
NanoSIP: NanoSIMS Applications for Microbial Biology
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/10.1007/978-981-97-5565-3_29openalex-snapshot
Invasive Fungal Infection in Hematological Malignancies
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inferred← citeshttps://doi.org/10.1007/s00425-015-2301-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00572-020-00934-2openalex-snapshot
Orchids and their mycorrhizal fungi: an insufficiently explored relationship
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/s00572-025-01221-8openalex-snapshot
The influence of mycorrhizal hyphal connections and neighbouring plants on Plantago lanceolata physiology and nutrient uptake
inferred← citeshttps://doi.org/10.1007/s00572-026-01303-1openalex-snapshot
Fatty acid signatures distinguish autotrophy, partial mycoheterotrophy, and full mycoheterotrophy in angiosperms
inferred← citeshttps://doi.org/10.1007/s13199-020-00681-0openalex-snapshot
Relative effectiveness of Tulasnella fungal strains in orchid mycorrhizal symbioses between germination and subsequent seedling growth
inferred← citeshttps://doi.org/10.1007/s42729-019-00026-xopenalex-snapshot
Orchid Mycorrhizal Interactions on the Pacific Side of the Andes from Chile. A Review
inferred← citeshttps://doi.org/10.1016/j.copbio.2016.06.007openalex-snapshot
Tracking microbial interactions with NanoSIMS
inferred← citeshttps://doi.org/10.1016/j.egg.2017.06.004openalex-snapshot
Culturable fungal endophytes in shoots of Dendrobium aqueum Lindley – An imperiled orchid
inferred← citeshttps://doi.org/10.1016/j.funbio.2022.06.001openalex-snapshot
Cryptostylis species (Orchidaceae) from a broad geographic and habitat range associate with a phylogenetically narrow lineage of Tulasnellaceae fungi
inferred← citeshttps://doi.org/10.1016/j.plantsci.2015.06.021openalex-snapshot
K+ accumulation in the cytoplasm and nucleus of the salt gland cells of Limonium bicolor accompanies increased rates of salt secretion under NaCl treatment using NanoSIMS
inferred← citeshttps://doi.org/10.1016/j.plantsci.2017.06.015openalex-snapshot
Cell-specific expression of plant nutrient transporter genes in orchid mycorrhizae
inferred← citeshttps://doi.org/10.1016/j.rhisph.2017.04.016openalex-snapshot
Using stable isotopes to explore root-microbe-mineral interactions in soil
inferred← citeshttps://doi.org/10.1016/j.sajb.2024.09.056openalex-snapshot
Effectiveness of symbiotic fungus Coprinellus radians on seeds germination and seedlings development of Cremastra appendiculata (D.Don.) Makino (Orchidaceae)
inferred← citeshttps://doi.org/10.1016/j.scienta.2021.110724openalex-snapshot
Mycorrhizal fungus Coprinellus disseminatus influences seed germination of the terrestrial orchid Cremastra appendiculata (D. Don) Makino
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Root-associated Helotiales fungi: Overlooked players in plant nutrition
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More than Pictures: When MS Imaging Meets Histology
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Orchids acquire fungal carbon for seed germination: pathways and players
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iTRAQ and RNA-Seq Analyses Provide New Insights into Regulation Mechanism of Symbiotic Germination of Dendrobium officinale Seeds (Orchidaceae)
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Biological explorations with nanoscale secondary ion mass spectrometry
inferred← citeshttps://doi.org/10.1073/pnas.1710455114openalex-snapshot
Root-associated fungal microbiota of nonmycorrhizal Arabis alpina and its contribution to plant phosphorus nutrition
inferred← citeshttps://doi.org/10.1093/aob/mcaa093openalex-snapshot
Orchid conservation: from theory to practice
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/mcw220openalex-snapshot
Comparative seed germination and seedling development of the ghost orchid, Dendrophylax lindenii (Orchidaceae), and molecular identification of its mycorrhizal fungus from South Florida
inferred← citeshttps://doi.org/10.1093/aob/mcx064openalex-snapshot
Exploring fungus–plant N transfer in a tripartite ant–plant–fungus mutualism
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/10.1111/1365-2745.12274openalex-snapshot
Photosynthesis in perennial mixotrophic Epipactis spp. (Orchidaceae) contributes more to shoot and fruit biomass than to hypogeous survival
inferred← citeshttps://doi.org/10.1111/1365-2745.70289openalex-snapshot
Enhanced below‐ground functioning is associated with higher plant resistance against drought: Implications for ecosystem functions
inferred← citeshttps://doi.org/10.1111/1462-2920.14244openalex-snapshot
Phenazine‐1‐carboxylic acid and soil moisture influence biofilm development and turnover of rhizobacterial biomass on wheat root surfaces
inferred← citeshttps://doi.org/10.1111/ele.13399openalex-snapshot
Angiosperm symbioses with non‐mycorrhizal fungal partners enhance N acquisition from ancient organic matter in a warming maritime Antarctic
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/nph.12769openalex-snapshot
The latest news from biological interactions in orchids: in love, head to toe
inferred← citeshttps://doi.org/10.1111/nph.13138openalex-snapshot
Exploring the transfer of recent plant photosynthates to soil microbes: mycorrhizal pathway vs direct root exudation
inferred← citeshttps://doi.org/10.1111/nph.14357openalex-snapshot
Nitrogen transport in the orchid mycorrhizal symbiosis – further evidence for a mutualistic association
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Unearthing the plant–microbe quid pro quo in root associations with beneficial fungi
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Novel insights into orchid mycorrhiza functioning from stable isotope signatures of fungal pelotons
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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
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Rôle du microbiote racinaire dans la nutrition phosphorée des plantes non-mycorhiziennes
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