scholarly article | Q13442814 |
P50 | author | Marc-André Selosse | Q21391695 |
Hans Jacquemyn | Q57445637 | ||
Rein Brys | Q113363468 | ||
P2093 | author name string | Michael Waud | |
Pierre-Emmanuel Courty | |||
Félix Lallemand | |||
Alicja Robionek | |||
P2860 | cites work | Variation in mycorrhizal associations with tulasnelloid fungi among populations of five Dactylorhiza species | Q21560777 |
GenBank | Q22065976 | ||
Basic local alignment search tool | Q25938991 | ||
Giving and receiving: measuring the carbon cost of mycorrhizas in the green orchid, Goodyera repens. | Q50627945 | ||
Partial mycoheterotrophy is more widespread among orchids than previously assumed. | Q51309412 | ||
Mycorrhizal interactions of orchids colonizing Estonian mine tailings hills. | Q51695010 | ||
New primers to amplify the fungal ITS2 region--evaluation by 454-sequencing of artificial and natural communities. | Q53101851 | ||
Changing partners in the dark: isotopic and molecular evidence of ectomycorrhizal liaisons between forest orchids and trees. | Q55038858 | ||
Cutadapt removes adapter sequences from high-throughput sequencing reads | Q55953584 | ||
Evolution of nutritional modes of Ceratobasidiaceae (Cantharellales, Basidiomycota) as revealed from publicly available ITS sequences | Q57180777 | ||
An island biogeographical view of the successional pathway in wet dune slacks | Q57267285 | ||
Improving indicator species analysis by combining groups of sites | Q58192868 | ||
Analysis of network architecture reveals phylogenetic constraints on mycorrhizal specificity in the genus Orchis (Orchidaceae) | Q58827536 | ||
Immigrant and extrinsic hybrid seed inviability contribute to reproductive isolation between forest and dune ecotypes of Epipactis helleborine (Orchidaceae) | Q59159770 | ||
Do chlorophyllous orchids heterotrophically use mycorrhizal fungal carbon? | Q85670557 | ||
Nitrogen and carbon stable isotope abundances support the myco-heterotrophic nature and host-specificity of certain achlorophyllous plants | Q29391673 | ||
UCHIME improves sensitivity and speed of chimera detection | Q29547664 | ||
UPARSE: highly accurate OTU sequences from microbial amplicon reads | Q29616627 | ||
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 | ||
Fungal specificity bottlenecks during orchid germination and development | Q33351742 | ||
Epipactis helleborine shows strong mycorrhizal preference towards ectomycorrhizal fungi with contrasting geographic distributions in Japan | Q33355522 | ||
Low specificity and nested subset structure characterize mycorrhizal associations in five closely related species of the genus Orchis | Q33671399 | ||
The contribution of DNA metabarcoding to fungal conservation: diversity assessment, habitat partitioning and mapping red-listed fungi in protected coastal Salix repens communities in the Netherlands | Q33768969 | ||
Green plants that feed on fungi: facts and questions about mixotrophy | Q34015751 | ||
Shifts in mycorrhizal fungi during the evolution of autotrophy to mycoheterotrophy in Cymbidium (Orchidaceae). | Q34327058 | ||
Does mycorrhizal specificity affect orchid decline and rarity? | Q34432713 | ||
Inefficient photosynthesis in the Mediterranean orchid Limodorum abortivum is mirrored by specific association to ectomycorrhizal Russulaceae | Q34489916 | ||
The evolutionary history of mycorrhizal specificity among lady's slipper orchids | Q34579932 | ||
Mycorrhizal fungal communities in coastal sand dunes and heaths investigated by pyrosequencing analyses | Q35544258 | ||
Mycorrhizal networks and coexistence in species-rich orchid communities | Q35547796 | ||
Habitat-driven variation in mycorrhizal communities in the terrestrial orchid genus Dactylorhiza | Q36203271 | ||
You are what you get from your fungi: nitrogen stable isotope patterns in Epipactis species | Q36320265 | ||
Saprotrophic fungal mycorrhizal symbionts in achlorophyllous orchids: finding treasures among the 'molecular scraps'? | Q37671510 | ||
Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi | Q39566006 | ||
Spatial repartition and genetic relationship of green and albino individuals in mixed populations of Cephalanthera orchids | Q39856079 | ||
Differences in mycorrhizal communities between Epipactis palustris, E. helleborine and its presumed sister species E. neerlandica | Q39945172 | ||
Two widespread green Neottia species (Orchidaceae) show mycorrhizal preference for Sebacinales in various habitats and ontogenetic stages | Q41542248 | ||
Temporal patterns of orchid mycorrhizal fungi in meadows and forests as revealed by 454 pyrosequencing | Q41641929 | ||
Are carbon and nitrogen exchange between fungi and the orchid Goodyera repens affected by irradiance? | Q41652974 | ||
Symbiotic germination capability of four Epipactis species (Orchidaceae) is broader than expected from adult ecology | Q42652925 | ||
Carbon and nitrogen supply to the underground orchid, Rhizanthella gardneri. | Q43114713 | ||
Photosynthetic Mediterranean meadow orchids feature partial mycoheterotrophy and specific mycorrhizal associations. | Q43464767 | ||
Identification of mycorrhizal fungi from single pelotons of Dactylorhiza majalis (Orchidaceae) using single-strand conformation polymorphism and mitochondrial ribosomal large subunit DNA sequences | Q43490481 | ||
Internal transcribed spacer primers and sequences for improved characterization of basidiomycetous orchid mycorrhizas. | Q44355022 | ||
Mycorrhizal specificity does not limit the distribution of an endangered orchid species | Q46431090 | ||
Demographic shifts related to mycoheterotrophy and their fitness impacts in two Cephalanthera species | Q46510903 | ||
Impact of primer choice on characterization of orchid mycorrhizal communities using 454 pyrosequencing | Q46941770 | ||
Coexisting orchid species have distinct mycorrhizal communities and display strong spatial segregation | Q46961175 | ||
Mixotrophy of Platanthera minor, an orchid associated with ectomycorrhiza-forming Ceratobasidiaceae fungi | Q48055257 | ||
P921 | main subject | mycorrhiza | Q99974 |
mixotrophy | Q112679667 | ||
P304 | page(s) | 1497 | |
P577 | publication date | 2017-08-29 | |
P1433 | published in | Frontiers in Plant Science | Q27723840 |
P1476 | title | Mycorrhizal Associations and Trophic Modes in Coexisting Orchids: An Ecological Continuum between Auto- and Mixotrophy | |
P478 | volume | 8 |
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