Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 53 checked references that resolve
resolves10.1139/b06-101<i>Cephalanthera longifolia</i> (Neottieae, Orchidaceae) is mixotrophic: a comparative study between green and nonphotosynthetic individuals
resolves10.1098/rspb.2004.2807Changing partners in the dark: isotopic and molecular evidence of ectomycorrhizal liaisons between forest orchids and trees
resolves10.3732/ajb.0900292Isotopic evidence of partial mycoheterotrophy in the Gentianaceae: <i>Bartonia virginica</i> and <i>Obolaria virginica</i> as case studies
resolves10.1046/j.1469-8137.2003.00872.x<sup>15</sup>N and <sup>13</sup>C natural abundance of autotrophic and myco‐heterotrophic orchids provides insight into nitrogen and carbon gain from fungal association
resolves10.1007/BF00325257Carbon and nitrogen isotope ratios in different compartments of a healthy and a declining Picea abies forest in the Fichtelgebirge, NE Bavaria
resolves10.1111/nph.13865Partial mycoheterotrophy is more widespread among orchids than previously assumed
resolves10.1111/1365-2745.12274Photosynthesis in perennial mixotrophic <i>Epipactis</i> spp. (Orchidaceae) contributes more to shoot and fruit biomass than to hypogeous survival
resolves10.1093/aob/mcw119Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi
resolves10.1093/aob/mcw015Differences in mycorrhizal communities between<i>Epipactis palustris</i>,<i>E. helleborine</i>and its presumed sister species<i>E. neerlandica</i>
resolves10.1093/bioinformatics/bts199Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
resolves10.1111/mec.12481Towards a unified paradigm for sequence‐based identification of fungi
resolves10.3732/ajb.0900354C and N stable isotope signatures reveal constraints to nutritional modes in orchids from the Mediterranean and Macaronesia
resolves10.1038/nature08867Périgord black truffle genome uncovers evolutionary origins and mechanisms of symbiosis
resolves10.1007/s00572-008-0187-0Epipactis helleborine shows strong mycorrhizal preference towards ectomycorrhizal fungi with contrasting geographic distributions in Japan
resolves10.1080/10256010802507458A methodological approach to improve estimates of nutrient gains by partially myco-heterotrophic plants†
resolves10.1098/rspb.2009.1966Irradiance governs exploitation of fungi: fine-tuning of carbon gain by two partially myco-heterotrophic orchids
resolves10.1128/AEM.01541-09Introducing mothur: Open-Source, Platform-Independent, Community-Supported Software for Describing and Comparing Microbial Communities
resolves10.3732/ajb.95.2.156Mycorrhizal interactions of orchids colonizing Estonian mine tailings hills
resolves10.1111/j.1469-8137.2010.03510.xThe degree of mycoheterotrophic carbon gain in green, variegated and vegetative albino individuals of <i>Cephalanthera damasonium</i> is related to leaf chlorophyll concentrations
resolves10.1111/nph.12688Carbon and nitrogen gain during the growth of orchid seedlings in nature
resolves10.1007/s00442-006-0581-2Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae
resolves10.3732/ajb.1100503Symbiotic germination capability of four <i>Epipactis</i> species (Orchidaceae) is broader than expected from adult ecology
resolves10.1046/j.1469-8137.2003.00876.xNitrogen and carbon stable isotope abundances support the myco‐heterotrophic nature and host‐specificity of certain achlorophyllous plants
resolves10.4319/lo.2001.46.8.2061Variation in δ<sup>15</sup>N and δ<sup>13</sup>C trophic fractionation: Implications for aquatic food web studies
resolves10.1111/j.1469-8137.2007.02065.xWide geographical and ecological distribution of nitrogen and carbon gains from fungi in pyroloids and monotropoids (Ericaceae) and in orchids
The 16 references without a DOI — listed, not checked
no DOI — not checkedIsotopic evidence of partial mycoheterotrophy in Burmannia coelestis (Burmanniaceae)
no DOI — not checkedYou are what you eat (plus a few permil): the carbon isotope cycle in food chains
no DOI — not checkedA rapid DNA isolation procedure for small quantities of fresh leaf tissue
no DOI — not checkedZeigerwerte von Pflanzen in Mitteleuropa
no DOI — not checkedStable isotope ecology
no DOI — not checkedAuf Spurensuche in der Natur: Stabile Isotope in der ökologischen Forschung. Rundgespräche der Kommission für Ökologie Bd. 30
no DOI — not checkedA simple sequentially rejective multiple test procedure
no DOI — not checkedChanges in the diversity of the mycorrhizal fungi of orchids as a function of the water supply of the habitat
no DOI — not checkedPartial mycoheterotrophy in Pyroleae: nitrogen and carbon stable isotope signatures during development from seedling to adult
no DOI — not checkedIntraspecific ITS variability in the Kingdom Fungi as expressed in the international sequence databases and its implications for molecular species identification
no DOI — not checkedCould orchids indicate truffle habitats? Mycorrhizal association between orchids and truffles
no DOI — not checkedR: A language and environment for statistical computing
no DOI — not checkedTerrestrial orchids from seed to mycotrophic plant
no DOI — not checkedChlorophyllous and achlorophyllous specimens of Epipactis microphylla (Neottieae, Orchidaceae) are associated with ectomycorrhizal Septomycetes, including Truffles
no DOI — not checkedkey
20170718092508_mcw265-B64
no DOI — not checkedPCR protocols: a guide to methods and applications
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