review article | Q7318358 |
scholarly article | Q13442814 |
P356 | DOI | 10.1038/NRMICRO.2016.59 |
P698 | PubMed publication ID | 27296482 |
P50 | author | Peter G Kennedy | Q90736754 |
Kabir G. Peay | Q51175931 | ||
P2093 | author name string | Jennifer M Talbot | |
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Herbivores cause a rapid increase in hereditary symbiosis and alter plant community composition | Q24530211 | ||
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Rat invasion of islands alters fungal community structure, but not wood decomposition rates | Q57055906 | ||
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Considering fungal:bacterial dominance in soils – Methods, controls, and ecosystem implications | Q57265055 | ||
Dispersal may limit the occurrence of specialist wood decay fungi already at small spatial scales | Q57596855 | ||
A fondness for fungi | Q59079136 | ||
Leaf endophytes andPopulusgenotype affect severity of damage from the necrotrophic leaf pathogen,Drepanopeziza populi | Q60242370 | ||
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Nuclear ribosomal internal transcribed spacer (ITS) region as a universal DNA barcode marker for Fungi | Q24630304 | ||
Yeast forms dominate fungal diversity in the deep oceans | Q24654921 | ||
Fungal communities associated with degradation of polyester polyurethane in soil | Q24679681 | ||
The fastest flights in nature: high-speed spore discharge mechanisms among fungi | Q27300125 | ||
Fungal traits that drive ecosystem dynamics on land | Q28082700 | ||
The plant immune system | Q28131801 | ||
Convergent losses of decay mechanisms and rapid turnover of symbiosis genes in mycorrhizal mutualists | Q28257614 | ||
A virus in a fungus in a plant: three-way symbiosis required for thermal tolerance | Q28285203 | ||
The human mycobiome in health and disease | Q28295636 | ||
Simultaneous amplicon sequencing to explore co-occurrence patterns of bacterial, archaeal and eukaryotic microorganisms in rumen microbial communities | Q28709077 | ||
Evidence for a persistent microbial seed bank throughout the global ocean | Q28709582 | ||
The fungus Armillaria bulbosa is among the largest and oldest living organisms | Q29030305 | ||
Bacterial community variation in human body habitats across space and time | Q29547432 | ||
Microbial biogeography: putting microorganisms on the map | Q29614465 | ||
Emerging fungal threats to animal, plant and ecosystem health | Q29616753 | ||
The diversity and biogeography of soil bacterial communities | Q29617328 | ||
Geographical distribution of fungi | Q30048372 | ||
CO2-enrichment and nutrient availability alter ectomycorrhizal fungal communities | Q30825253 | ||
Low diversity and high host preference of ectomycorrhizal fungi in western Amazonia, a neotropical biodiversity hotspot | Q30940278 | ||
Global patterns in bacterial diversity | Q33288814 | ||
Molecular evidence for long distance dispersal across the Southern Hemisphere in the Ganoderma applanatum-australe species complex (Basidiomycota). | Q33322061 | ||
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 | ||
Characterization of the oral fungal microbiome (mycobiome) in healthy individuals | Q33523794 | ||
Assembly history dictates ecosystem functioning: evidence from wood decomposer communities | Q33562082 | ||
Indoor fungal composition is geographically patterned and more diverse in temperate zones than in the tropics. | Q33628384 | ||
Endemism and functional convergence across the North American soil mycobiome | Q33674072 | ||
A single European aspen (Populus tremula) tree individual may potentially harbour dozens of Cenococcum geophilum ITS genotypes and hundreds of species of ectomycorrhizal fungi | Q33757702 | ||
Leaf and root-associated fungal assemblages do not follow similar elevational diversity patterns | Q33817412 | ||
Ectomycorrhizal fungi in Mexican Alnus forests support the host co-migration hypothesis and continental-scale patterns in phylogeography | Q33823805 | ||
Drivers of bacterial beta-diversity depend on spatial scale | Q33881732 | ||
Discovery of novel intermediate forms redefines the fungal tree of life | Q33895964 | ||
Extensive sampling of basidiomycete genomes demonstrates inadequacy of the white-rot/brown-rot paradigm for wood decay fungi | Q33919794 | ||
Active and total microbial communities in forest soil are largely different and highly stratified during decomposition | Q33966880 | ||
Ectomycorrhizal fungal diversity and community structure on three co-occurring leguminous canopy tree species in a Neotropical rainforest | Q34007391 | ||
Do assembly history effects attenuate from species to ecosystem properties? A field test with wood-inhabiting fungi. | Q51576556 | ||
Inhospitable sweetness: nectar filtering of pollinator-borne inocula leads to impoverished, phylogenetically clustered yeast communities. | Q51645856 | ||
Marine fungi: their ecology and molecular diversity | Q34212351 | ||
Beyond biogeographic patterns: processes shaping the microbial landscape. | Q34266945 | ||
Fungal endophyte communities reflect environmental structuring across a Hawaiian landscape. | Q34353559 | ||
Priority effects determine the outcome of ectomycorrhizal competition between two Rhizopogon species colonizing Pinus muricata seedlings | Q34409998 | ||
Untangling the fungal niche: the trait-based approach | Q34433754 | ||
Assembly of complex plant-fungus networks. | Q34446533 | ||
Biogeography of ectomycorrhizal fungi associated with alders (Alnus spp.) in relation to biotic and abiotic variables at the global scale | Q34591537 | ||
Spatial separation of litter decomposition and mycorrhizal nitrogen uptake in a boreal forest | Q34605190 | ||
The emerging world of the fungal microbiome | Q34727901 | ||
Topographic diversity of fungal and bacterial communities in human skin | Q34734628 | ||
Aerial dispersal of pathogens on the global and continental scales and its impact on plant disease | Q34762833 | ||
Meta-analysis of deep-sequenced fungal communities indicates limited taxon sharing between studies and the presence of biogeographic patterns | Q35013258 | ||
Towards a unified paradigm for sequence-based identification of fungi | Q35013467 | ||
Contrasting primary successional trajectories of fungi and bacteria in retreating glacier soils | Q35013501 | ||
Not as ubiquitous as we thought: taxonomic crypsis, hidden diversity and cryptic speciation in the cosmopolitan fungus Thelonectria discophora (Nectriaceae, Hypocreales, Ascomycota). | Q35034789 | ||
Ectomycorrhizal fungal traits reflect environmental conditions along a coastal California edaphic gradient | Q35056430 | ||
The lung mycobiome: an emerging field of the human respiratory microbiome. | Q35082308 | ||
Sequence depth, not PCR replication, improves ecological inference from next generation DNA sequencing | Q35108872 | ||
Spore dispersal of basidiomycete fungi at the landscape scale is driven by stochastic and deterministic processes and generates variability in plant-fungal interactions. | Q35197054 | ||
Soil fungal communities of grasslands are environmentally structured at a regional scale in the Alps | Q35209536 | ||
Global biogeography of Alnus-associated Frankia actinobacteria | Q35225196 | ||
Fungi identify the geographic origin of dust samples | Q35394294 | ||
Fungal biogeography. Global diversity and geography of soil fungi | Q35457192 | ||
Plant diversity predicts beta but not alpha diversity of soil microbes across grasslands worldwide | Q35457305 | ||
Phylogenetic signal in plant pathogen-host range | Q35691027 | ||
FUNGAL SYMBIONTS. Global assessment of arbuscular mycorrhizal fungus diversity reveals very low endemism. | Q35758058 | ||
Common foliar fungi of Populus trichocarpa modify Melampsora rust disease severity. | Q35840600 | ||
Living in a fungal world: impact of fungi on soil bacterial niche development | Q36231168 | ||
Immunity to fungi | Q36502318 | ||
Ectomycorrhizal fungi decompose soil organic matter using oxidative mechanisms adapted from saprotrophic ancestors | Q37333989 | ||
From dandruff to deep-sea vents: Malassezia-like fungi are ecologically hyper-diverse | Q38241886 | ||
Ectomycorrhizal fungi - potential organic matter decomposers, yet not saprotrophs | Q38294015 | ||
Carbon availability triggers the decomposition of plant litter and assimilation of nitrogen by an ectomycorrhizal fungus. | Q38500296 | ||
Determining place and process: functional traits of ectomycorrhizal fungi that affect both community structure and ecosystem function. | Q38553421 | ||
Pathogens and insect herbivores drive rainforest plant diversity and composition | Q38887710 | ||
The patchiness of epifoliar fungi in tropical forests: host range, host abundance, and environment | Q39023477 | ||
Lack of host specificity leads to independent assortment of dipterocarps and ectomycorrhizal fungi across a soil fertility gradient. | Q39345604 | ||
Extensive gene flow over Europe and possible speciation over Eurasia in the ectomycorrhizal basidiomycete Laccaria amethystina complex | Q39675849 | ||
Comment on "Global assessment of arbuscular mycorrhizal fungus diversity reveals very low endemism". | Q39970546 | ||
The ectomycorrhizal fungus Paxillus involutus converts organic matter in plant litter using a trimmed brown-rot mechanism involving Fenton chemistry | Q41965349 | ||
Coral-associated marine fungi form novel lineages and heterogeneous assemblages | Q42208795 | ||
Contrasting soil pH effects on fungal and bacterial growth suggest functional redundancy in carbon mineralization | Q43163262 | ||
Survey of fungi and yeast in polymicrobial infections in chronic wounds | Q44296416 | ||
Genetic isolation between two recently diverged populations of a symbiotic fungus | Q46434763 | ||
Changes in fungal communities along a boreal forest soil fertility gradient | Q46731644 | ||
Measuring ectomycorrhizal fungal dispersal: macroecological patterns driven by microscopic propagules. | Q46807296 | ||
Ectomycorrhizal Cortinarius species participate in enzymatic oxidation of humus in northern forest ecosystems | Q46906739 | ||
Comparisons of the fungal and protistan communities among different marine sponge holobionts by pyrosequencing | Q46926323 | ||
Dispersing misconceptions and identifying opportunities for the use of 'omics' in soil microbial ecology. | Q51157423 | ||
P433 | issue | 7 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | Earth | Q2 |
mycobiome | Q24975941 | ||
biodiversity | Q47041 | ||
P304 | page(s) | 434-447 | |
P577 | publication date | 2016-07-01 | |
P1433 | published in | Nature Reviews Microbiology | Q1071797 |
P1476 | title | Dimensions of biodiversity in the Earth mycobiome | |
P478 | volume | 14 |