scholarly article | Q13442814 |
P50 | author | Gerhard Gebauer | Q64878643 |
P2093 | author name string | Nicole A Hynson | |
Julienne M-I Schiebold | |||
P2860 | cites work | Two mycoheterotrophic orchids from Thailand tropical dipterocarpacean forests associate with a broad diversity of ectomycorrhizal fungi | Q21245327 |
Evidence for novel and specialized mycorrhizal parasitism: the orchid Gastrodia confusa gains carbon from saprotrophic Mycena | Q24652872 | ||
Myco-heterotrophy: when fungi host plants | Q24655338 | ||
A power primer | Q27861029 | ||
Epiparasitic plants specialized on arbuscular mycorrhizal fungi | Q28204344 | ||
Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae | Q28272784 | ||
Fine-level mycorrhizal specificity in the Monotropoideae (Ericaceae): specificity for fungal species groups | Q29013513 | ||
Nitrogen and carbon stable isotope abundances support the myco-heterotrophic nature and host-specificity of certain achlorophyllous plants | Q29391673 | ||
15N and 13C natural abundance of autotrophic and myco-heterotrophic orchids provides insight into nitrogen and carbon gain from fungal association | Q29395600 | ||
The evolutionary ecology of myco-heterotrophy | Q29544657 | ||
Simultaneous inference in general parametric models | Q29619454 | ||
Carbon Isotope Discrimination and Photosynthesis | Q29999511 | ||
Mixotrophy in orchids: insights from a comparative study of green individuals and nonphotosynthetic individuals of Cephalanthera damasonium | Q30781838 | ||
Chlorophyllous and achlorophyllous specimens of Epipactis microphylla,(Neottieae, Orchidaceae) are associated with ectomycorrhizal septomycetes, including truffles | Q33202262 | ||
Mycoheterotrophy evolved from mixotrophic ancestors: evidence in Cymbidium (Orchidaceae) | Q33649450 | ||
Green plants that feed on fungi: facts and questions about mixotrophy | Q34015751 | ||
Independent recruitment of saprotrophic fungi as mycorrhizal partners by tropical achlorophyllous orchids | Q34019019 | ||
High root concentration and uneven ectomycorrhizal diversity near Sarcodes sanguinea (Ericaceae): a cheater that stimulates its victims? | Q34512380 | ||
Carbon and nitrogen metabolism in mycorrhizal networks and mycoheterotrophic plants of tropical forests: a stable isotope analysis | Q34628832 | ||
Measuring carbon gains from fungal networks in understory plants from the tribe Pyroleae (Ericaceae): a field manipulation and stable isotope approach | Q34633890 | ||
The importance of associations with saprotrophic non-Rhizoctonia fungi among fully mycoheterotrophic orchids is currently under-estimated: novel evidence from sub-tropical Asia | Q35675112 | ||
Independent, specialized invasions of ectomycorrhizal mutualism by two nonphotosynthetic orchids | Q36137655 | ||
Elucidating the nutritional dynamics of fungi using stable isotopes | Q37339214 | ||
15N and 13C natural abundance of two mycoheterotrophic and a putative partially mycoheterotrophic species associated with arbuscular mycorrhizal fungi | Q39245858 | ||
Stable isotope signatures confirm carbon and nitrogen gain through ectomycorrhizas in the ghost orchid Epipogium aphyllum Swartz | Q43547131 | ||
Seasonal and environmental changes of mycorrhizal associations and heterotrophy levels in mixotrophic Pyrola japonica (Ericaceae) growing under different light environments | Q44313035 | ||
High-resolution secondary ion mass spectrometry analysis of carbon dynamics in mycorrhizas formed by an obligately myco-heterotrophic orchid | Q45079984 | ||
Wide geographical and ecological distribution of nitrogen and carbon gains from fungi in pyroloids and monotropoids (Ericaceae) and in orchids | Q46230484 | ||
Are there geographic mosaics of mycorrhizal specificity and partial mycoheterotrophy? A case study in Moneses uniflora (Ericaceae). | Q46696547 | ||
Partial mycoheterotrophy in Pyroleae: nitrogen and carbon stable isotope signatures during development from seedling to adult. | Q46814550 | ||
Carbon and nitrogen gain during the growth of orchid seedlings in nature | Q46944110 | ||
Foliar and fungal 15N:14N ratios reflect development of mycorrhizae and nitrogen supply during primary succession: testing analytical models | Q47301254 | ||
Post-photosynthetic fractionation of stable carbon isotopes between plant organs--a widespread phenomenon | Q47800202 | ||
The chlorophyll-containing orchid Corallorhiza trifida derives little carbon through photosynthesis | Q47917937 | ||
Mixotrophy of Platanthera minor, an orchid associated with ectomycorrhiza-forming Ceratobasidiaceae fungi | Q48055257 | ||
Isotopic evidence of partial mycoheterotrophy in the Gentianaceae: Bartonia virginica and Obolaria virginica as case studies. | Q50519880 | ||
The degree of mycoheterotrophic carbon gain in green, variegated and vegetative albino individuals of Cephalanthera damasonium is related to leaf chlorophyll concentrations | Q50537814 | ||
Isotopic evidence of full and partial myco-heterotrophy in the plant tribe Pyroleae (Ericaceae). | Q50598948 | ||
Nitrate, nitrate reduction and organic nitrogen in plants from different ecological and taxonomic groups of Central Europe. | Q51217327 | ||
Partial mycoheterotrophy is more widespread among orchids than previously assumed. | Q51309412 | ||
C and N stable isotope signatures reveal constraints to nutritional modes in orchids from the Mediterranean and Macaronesia. | Q51597299 | ||
Irradiance governs exploitation of fungi: fine-tuning of carbon gain by two partially myco-heterotrophic orchids. | Q51640712 | ||
Evidence of a myco-heterotroph in the plant family Ericaceae that lacks mycorrhizal specificity. | Q51650374 | ||
A methodological approach to improve estimates of nutrient gains by partially myco-heterotrophic plants. | Q51673492 | ||
The ectomycorrhizal specialist orchid Corallorhiza trifida is a partial myco-heterotroph. | Q51695292 | ||
Changing partners in the dark: isotopic and molecular evidence of ectomycorrhizal liaisons between forest orchids and trees. | Q55038858 | ||
The biology of myco-heterotrophic ('saprophytic') plants | Q55923403 | ||
Evolution of extreme specialization within a lineage of ectomycorrhizal epiparasites | Q56442503 | ||
Uses and misuses of meta-analysis in plant ecology | Q56450607 | ||
Why are non-photosynthetic tissues generally13C enriched compared with leaves in C3plants? Review and synthesis of current hypotheses | Q56965735 | ||
A Lego System for Conditional Inference | Q57066709 | ||
Implementing a Class of Permutation Tests: ThecoinPackage | Q57263834 | ||
Stable isotope cellular imaging reveals that both live and degenerating fungal pelotons transfer carbon and nitrogen to orchid protocorms | Q57866041 | ||
Assimilation and isotopic fractionation of nitrogen by mycorrhizal and nonmycorrhizal subarctic plants | Q58897494 | ||
Nutritional regulation in mixotrophic plants: new insights from Limodorum abortivum | Q64462280 | ||
delta(15)N as an integrator of the nitrogen cycle | Q73443029 | ||
Fungal hosts for mycoheterotrophic plants: a nonexclusive, but highly selective club | Q83962297 | ||
Do chlorophyllous orchids heterotrophically use mycorrhizal fungal carbon? | Q85670557 | ||
Carbon and nitrogen isotope ratios in different compartments of a healthy and a declining Picea abies forest in the Fichtelgebirge, NE Bavaria | Q87591458 | ||
P433 | issue | 3 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | stable isotope | Q878130 |
Myco-heterotrophy | Q2420488 | ||
Ectomycorrhiza | Q3047120 | ||
P1104 | number of pages | 13 | |
P304 | page(s) | 467-479 | |
P577 | publication date | 2016-07-24 | |
P1433 | published in | Annals of Botany | Q1821243 |
P1476 | title | Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi | |
P478 | volume | 118 |
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