scholarly article | Q13442814 |
P356 | DOI | 10.1111/J.1365-294X.2012.05666.X |
P698 | PubMed publication ID | 22703050 |
P50 | author | Thomas D. Bruns | Q47114763 |
Kabir G. Peay | Q51175931 | ||
P2093 | author name string | Nhu H Nguyen | |
Max G Schubert | |||
P2860 | cites work | QIIME allows analysis of high-throughput community sequencing data | Q24616873 |
Competition and Biodiversity in Spatially Structured Habitats | Q29028733 | ||
ITS primers with enhanced specificity for basidiomycetes--application to the identification of mycorrhizae and rusts | Q29547621 | ||
Ecological responses to recent climate change | Q29547682 | ||
Global dispersal of free-living microbial eukaryote species | Q29616777 | ||
The diversity and biogeography of soil bacterial communities | Q29617328 | ||
Geographic barriers isolate endemic populations of hyperthermophilic archaea | Q30969227 | ||
Community patterns in source-sink metacommunities | Q31025773 | ||
Spatial scaling of microbial eukaryote diversity | Q31135432 | ||
Productivity-biodiversity relationships depend on the history of community assembly. | Q31150458 | ||
Climate change and the future of California's endemic flora | Q31164679 | ||
Spatial patterns of seed dispersal, their determinants and consequences for recruitment. | Q52077390 | ||
Rapid quantification and taxonomic classification of environmental DNA from both prokaryotic and eukaryotic origins using a microarray. | Q52563829 | ||
Habitat destruction and the extinction debt | Q55879812 | ||
The Individualistic Concept of the Plant Association | Q56028230 | ||
AN EVALUATION OF TECHNIQUES FOR MEASURING VESICULAR ARBUSCULAR MYCORRHIZAL INFECTION IN ROOTS | Q56879291 | ||
Ectomycorrhizal fungal communities at forest edges | Q56965968 | ||
Size, distribution and biomass of genets in populations of Suillus bovinus (L.: Fr.) Roussel revealed by somatic incompatibility | Q56982456 | ||
The metacommunity concept: a framework for multi-scale community ecology | Q57012668 | ||
An open source software package for automated extraction of ITS1 and ITS2 from fungal ITS sequences for use in high-throughput community assays and molecular ecology | Q57055871 | ||
Mixed effects models and extensions in ecology with R | Q57623181 | ||
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS | Q58333605 | ||
Release and dispersal of basidiospores from Amanita muscaria var. alba and their infiltration into a residence | Q59205308 | ||
Fungal community analysis by large-scale sequencing of environmental samples | Q33223029 | ||
Emerging infectious disease and the loss of biodiversity in a Neotropical amphibian community | Q33234071 | ||
Dispersal limitations matter for microbial morphospecies | Q33243943 | ||
454 Pyrosequencing analyses of forest soils reveal an unexpectedly high fungal diversity | Q33496293 | ||
Potential link between plant and fungal distributions in a dipterocarp rainforest: community and phylogenetic structure of tropical ectomycorrhizal fungi across a plant and soil ecotone | Q33514091 | ||
Assembly history dictates ecosystem functioning: evidence from wood decomposer communities | Q33562082 | ||
Experimental tests of the bacterial distance-decay relationship | Q33599725 | ||
Indoor fungal composition is geographically patterned and more diverse in temperate zones than in the tropics. | Q33628384 | ||
Drivers of bacterial beta-diversity depend on spatial scale | Q33881732 | ||
Phylogenetic species recognition and species concepts in fungi | Q33928233 | ||
Microbes do not follow the elevational diversity patterns of plants and animals | Q33929014 | ||
95% of basidiospores fall within 1 m of the cap: a field-and modeling-based study | Q33941832 | ||
Biogeographic kinetics: estimation of relaxation times for avifaunas of southwest pacific islands | Q33994772 | ||
Ectomycorrhizal fungal diversity and community structure on three co-occurring leguminous canopy tree species in a Neotropical rainforest | Q34007391 | ||
Colonization-competition tradeoffs as a mechanism driving successional dynamics in ectomycorrhizal fungal communities | Q34031961 | ||
Priority effects determine the outcome of ectomycorrhizal competition between two Rhizopogon species colonizing Pinus muricata seedlings | Q34409998 | ||
Community diversity: relative roles of local and regional processes | Q34675652 | ||
Metagenomic and small-subunit rRNA analyses reveal the genetic diversity of bacteria, archaea, fungi, and viruses in soil | Q34683148 | ||
Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease | Q34762833 | ||
Evolutionary ecology of plant diseases in natural ecosystems | Q34766367 | ||
The microbial engines that drive Earth's biogeochemical cycles. | Q34780678 | ||
Extensive gene flow over Europe and possible speciation over Eurasia in the ectomycorrhizal basidiomycete Laccaria amethystina complex | Q39675849 | ||
Inoculum potential of Rhizopogon spores increases with time over the first 4 yr of a 99-yr spore burial experiment | Q45196252 | ||
Quantifying microbial communities with 454 pyrosequencing: does read abundance count? | Q45791356 | ||
Evidence of dispersal limitation in soil microorganisms: isolation reduces species richness on mycorrhizal tree islands | Q46528384 | ||
A strong species-area relationship for eukaryotic soil microbes: island size matters for ectomycorrhizal fungi. | Q46547361 | ||
Intra-specific and intra-sporocarp ITS variation of ectomycorrhizal fungi as assessed by rDNA sequencing of sporocarps and pooled ectomycorrhizal roots from a Quercus woodland | Q46718364 | ||
Lack of belowground mutualisms hinders Pinaceae invasions. | Q51180848 | ||
Spores of ectomycorrhizal fungi: ecological strategies for germination and dormancy. | Q51181237 | ||
Do assembly history effects attenuate from species to ecosystem properties? A field test with wood-inhabiting fungi. | Q51576556 | ||
Does a facultative mutualism limit species range expansion? | Q51605401 | ||
Root tip competition among ectomycorrhizal fungi: are priority effects a rule or an exception? | Q51650512 | ||
Concurrent niche and neutral processes in the competition-colonization model of species coexistence. | Q51703668 | ||
The effects of resource enrichment, dispersal, and predation on local and metacommunity structure. | Q51728445 | ||
P433 | issue | 16 | |
P921 | main subject | biological dispersal | Q778143 |
macroecology | Q1886501 | ||
Ectomycorrhiza | Q3047120 | ||
P304 | page(s) | 4122-4136 | |
P577 | publication date | 2012-06-15 | |
P1433 | published in | Molecular Ecology | Q6895946 |
P1476 | title | Measuring ectomycorrhizal fungal dispersal: macroecological patterns driven by microscopic propagules | |
P478 | volume | 21 |
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Q51150612 | Competition-colonization tradeoffs structure fungal diversity. |
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Q38919660 | Continental-level population differentiation and environmental adaptation in the mushroom Suillus brevipes |
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Q34593499 | Dispersal in microbes: fungi in indoor air are dominated by outdoor air and show dispersal limitation at short distances |
Q39373953 | Diversity and Structure of Fungal Communities in Neotropical Rainforest Soils: The Effect of Host Recurrence |
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Q40950654 | Ectomycorrhizal fungal communities coinvading with Pinaceae host plants in Argentina: Gringos bajo el bosque |
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Q31065433 | Ectomycorrhizal fungal richness declines towards the host species' range edge |
Q33457697 | Ectomycorrhizal fungal spore bank recovery after a severe forest fire: some like it hot |
Q91313636 | Ectomycorrhizas and tree seedling establishment are strongly influenced by forest edge proximity but not soil inoculum |
Q46505936 | Effects of dispersal and selection on stochastic assembly in microbial communities |
Q57596843 | Effects of ecological continuity on species richness and composition in forests and woodlands: A review |
Q33674072 | Endemism and functional convergence across the North American soil mycobiome |
Q35189393 | Environmental controls on fungal community composition and abundance over 3 years in native and degraded shrublands. |
Q35854778 | Environmental switching during biofilm development in a cold seep system and functional determinants of species sorting |
Q91644531 | Evaluation of host effects on ectomycorrhizal fungal community compositions in a forested landscape in northern Japan |
Q37324326 | Evolution of uni- and bifactorial sexual compatibility systems in fungi |
Q34796122 | Exotic mammals disperse exotic fungi that promote invasion by exotic trees |
Q88359026 | Explaining European fungal fruiting phenology with climate variability |
Q111627814 | Fire as a driver of fungal diversity — A synthesis of current knowledge |
Q31095472 | Fire-severity effects on plant-fungal interactions after a novel tundra wildfire disturbance: implications for arctic shrub and tree migration |
Q40471149 | Forest microbiome: diversity, complexity and dynamics. |
Q91697460 | Fungal aerobiota are not affected by time nor environment over a 13-y time series at the Mauna Loa Observatory |
Q35023582 | Fungi at a small scale: spatial zonation of fungal assemblages around single trees |
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Q46434763 | Genetic isolation between two recently diverged populations of a symbiotic fungus |
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Q55499621 | Network hubs in root-associated fungal metacommunities. |
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Q40899493 | Population genomic analyses reveal possible drivers of population divergence |
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