2004
DOI: 10.1007/s11557-006-0075-y
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Taxon-specific fungal primers reveal unexpectedly high diversity during leaf decomposition in a stream

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Cited by 150 publications
(100 citation statements)
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“…The fungal community on plant litter decomposing in aquatic ecosystems is largely dominated by aquatic hyphomycetes (72), but other fungal groups like Ascomycota (8,19), Oomycota, Zygomycota (3), and Chytridiomycota have also been reported [43]). Using taxon-specific primers, Nikolcheva and Bärlocher (43) demonstrated the presence of these major fungal taxa and found ascomycetes to be the main group of fungi colonizing decaying leaves in streams.…”
Section: Vol 73 2007 Microbial Diversity On Leaf Litter As Determinmentioning
confidence: 99%
See 1 more Smart Citation
“…The fungal community on plant litter decomposing in aquatic ecosystems is largely dominated by aquatic hyphomycetes (72), but other fungal groups like Ascomycota (8,19), Oomycota, Zygomycota (3), and Chytridiomycota have also been reported [43]). Using taxon-specific primers, Nikolcheva and Bärlocher (43) demonstrated the presence of these major fungal taxa and found ascomycetes to be the main group of fungi colonizing decaying leaves in streams.…”
Section: Vol 73 2007 Microbial Diversity On Leaf Litter As Determinmentioning
confidence: 99%
“…Recently, in leaf decomposition studies, molecular methods have been employed to look at microbial diversity to circumvent inadequacies of culture-based methods (5,43). Denaturing gradient gel electrophoresis (DGGE) has been used extensively for examination of complex microbial community assemblages (6,20,30,46,52).…”
mentioning
confidence: 99%
“…Both allochthonous leaf litter and submerged wood in streams harbor diverse communities of fungi, mainly ascomycetes and their anamorphs (hyphomycetes) (see, e.g., references 4, 39, and 51) though chytrids, zygomycetes, and basidiomycetes have also been detected by using molecular techniques (35). Communities can be species rich.…”
mentioning
confidence: 99%
“…DNA fragments spanning rDNA ITS were amplified using the primers ITS1F and ITS4, and low-quality products were reamplified using ITS1 and ITS4 [36]. Double products were amplified from genomic DNA again using specific primers for basidiomycetes (ITS1F, ITS4Basidio; [7,37]) and ascomycetes (ITS5, ITS4Asco; [7,37]) in order to separate products. PCR condition used an initial cycle of 150 s at 94 °C, followed by 37 cycles of 30 s at 94 °C, 40 s at 50 °C, 30 s at 72 °C and a 270-s final extension at 72 °C.…”
Section: Root Sampling and Identification Of Ectomycorrhizasmentioning
confidence: 99%