Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae
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Two mycoheterotrophic orchids from Thailand tropical dipterocarpacean forests associate with a broad diversity of ectomycorrhizal fungiMyco-heterotrophy: when fungi host plantsThe carbon and nitrogen ecophysiologies of two endemic tropical orchids mirrors those of their temperate relatives and the local environmentNew species of Tomentella (Thelephorales) from the Patagonian Andes forests.Diversity of fungi in hair roots of Ericaceae varies along a vegetation gradient.Mycoheterotrophy evolved from mixotrophic ancestors: evidence in Cymbidium (Orchidaceae)Phylogeny of Pyroleae (Ericaceae): implications for character evolution.Measuring carbon gains from fungal networks in understory plants from the tribe Pyroleae (Ericaceae): a field manipulation and stable isotope approach.Variation in nutrient-acquisition patterns by mycorrhizal fungi of rare and common orchids explains diversification in a global biodiversity hotspot.Evidence from population genetics that the ectomycorrhizal basidiomycete Laccaria amethystina is an actual multihost symbiont.Sebacinales - one thousand and one interactions with land plants.Experimental evidence of ericoid mycorrhizal potential within Serendipitaceae (Sebacinales).Pyrola japonica, a partially mycoheterotrophic Ericaceae, has mycorrhizal preference for russulacean fungi in central Japan.Mixotrophy everywhere on land and in water: the grand écart hypothesis.You are what you get from your fungi: nitrogen stable isotope patterns in Epipactis species.Mixotrophy in Pyroleae (Ericaceae) from Estonian boreal forests does not vary with light or tissue age.15N and 13C natural abundance of two mycoheterotrophic and a putative partially mycoheterotrophic species associated with arbuscular mycorrhizal fungi.Plant family identity distinguishes patterns of carbon and nitrogen stable isotope abundance and nitrogen concentration in mycoheterotrophic plants associated with ectomycorrhizal fungi.Two widespread green Neottia species (Orchidaceae) show mycorrhizal preference for Sebacinales in various habitats and ontogenetic stages.Comparative analysis of plastid genomes of non-photosynthetic Ericaceae and their photosynthetic relatives.Enkianthus campanulatus (Ericaceae) is commonly associated with arbuscular mycorrhizal fungi.Root-associated fungal communities in three Pyroleae species and their mycobiont sharing with surrounding trees in subalpine coniferous forests on Mount Fuji, Japan.Fungal host specificity is not a bottleneck for the germination of Pyroleae species (Ericaceae) in a Bavarian forest.High-resolution secondary ion mass spectrometry analysis of carbon dynamics in mycorrhizas formed by an obligately myco-heterotrophic orchid.Wide geographical and ecological distribution of nitrogen and carbon gains from fungi in pyroloids and monotropoids (Ericaceae) and in orchids.Specificity of fungal associations of Pyroleae and Monotropa hypopitys during germination and seedling development.Are there geographic mosaics of mycorrhizal specificity and partial mycoheterotrophy? A case study in Moneses uniflora (Ericaceae).Mycorrhizal fungi associated with Monotropastrum humile (Ericaceae) in central Japan.Partial mycoheterotrophy in Pyroleae: nitrogen and carbon stable isotope signatures during development from seedling to adult.Hydrogen peroxide staining to visualize intracellular bacterial infections of seedling root cells.Carbon and nitrogen gain during the growth of orchid seedlings in nature.A hemiparasite in the forest understorey: photosynthetic performance and carbon balance of Melampyrum pratense.The elusive predisposition to mycoheterotrophy in Ericaceae.Mixotrophy of Platanthera minor, an orchid associated with ectomycorrhiza-forming Ceratobasidiaceae fungi.Is it better to give than to receive? A stable isotope perspective on orchid-fungal carbon transport in the green orchid species Goodyera repens and Goodyera oblongifolia.Mycoheterotrophic germination of Pyrola asarifolia dust seeds reveals convergences with germination in orchids.Irradiance governs exploitation of fungi: fine-tuning of carbon gain by two partially myco-heterotrophic orchids.Evidence of a myco-heterotroph in the plant family Ericaceae that lacks mycorrhizal specificity.A methodological approach to improve estimates of nutrient gains by partially myco-heterotrophic plants.Interactions of fungi with other organisms
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P2860
Parallel evolutionary paths to mycoheterotrophy in understorey Ericaceae and Orchidaceae: ecological evidence for mixotrophy in Pyroleae
description
2007 nî lūn-bûn
@nan
2007 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի մարտին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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Parallel evolutionary paths to ...... nce for mixotrophy in Pyroleae
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P2093
Prune Pellet
P2888
P304
P3181
P356
10.1007/S00442-006-0581-2
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2007-03-01T00:00:00Z
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P6179
1038274904