Fungal Ecology

Papers
(The median citation count of Fungal Ecology is 3. The table below lists those papers that are above that threshold based on CrossRef citation counts [max. 250 papers]. The publications cover those that have been published in the past four years, i.e., from 2021-09-01 to 2025-09-01.)
ArticleCitations
Editorial Board67
Fungal ecology at treelines29
Effects of fungicide application on the foliar endophytic fungi of Scots pine (Pinus sylvestris)28
Intrinsic growth rate and cellobiohydrolase activity underlie the phylogenetic signal to fungal decomposer succession23
Climate change and plant-microbe interactions: Water-availability influences the effective specialization of a fungal pathogen17
Electrical potentials in the ectomycorrhizal fungus Laccaria bicolor after a rainfall event17
Nitrogen addition drives changes in arbuscular mycorrhizal fungal richness through changes in plant species richness in revegetated alpine grassland17
Editorial board16
Editorial board16
Interaction between growth environment and host progeny shape fungal endophytic assemblages in transplanted Fagus sylvatica14
Decreased diversity and connectivity of endophytic fungal assemblages within cultivated European olive trees compared to their native African counterpart14
Transcriptomic and protein analysis of Trametes versicolor interacting with a Hypholoma fasciculare mycelium foraging in soil13
Shifts in root-associated fungal communities under drought conditions in Ricinus communis13
Ratio-dependent functional response of two common Cladocera present in farmland ponds to Batrachochytrium dendrobatidis13
Carbon allocation shifts during fungal mycelial competition under the heat stress12
Fungal community composition and diversity in the rhizosphere soils of Argentina (syn. Potentilla) anserina, on the Qinghai Plateau11
Diurnal patterns and conidial dynamics of Batkoa major, a generalist entomophthoralean pathogen11
Fine-scale genetic diversity and genet dynamics of the fairy ring fungus Floccularia luteovirens on the Qinghai–Tibet plateau11
Non-invasive monitoring of photosynthetic activity and water content in forest lichens by spectral reflectance data and RGB colors from photographs10
Crown closure affects endophytic leaf mycobiome compositional dynamics over time in Pseudotsuga menziesii var. menziesii10
Impact of Norway spruce pre-degradation stages induced by Gloeophyllum trabeum on fungal and bacterial communities10
Environmental heterogeneity and soil properties influence fungal communities in Amazonian ferruginous fields10
Ecological niche modelling of Cantharellus species in Benin, and revision of their conservation status10
Size, age, and insights into establishment, dynamics and persistence of fairy rings in the Laramie Basin, Wyoming10
Specific network and phylosymbiosis pattern in endophyte community of coastal halophytes9
Influence of Batrachochytrium dendrobatidis isolate and dose on infection outcomes in a critically endangered Australian amphibian9
Metatranscriptomic analyses of grapes reveal differences in expressed functional genes of filamentous and yeast fungi during noble rot and grey rot9
Editorial board9
Microhabitat diversity – A crucial factor shaping macrofungal communities and morphological trait expression in dead wood9
Deadwood substrate and species-species interactions determine the release of volatile organic compounds by wood-decaying fungi9
The role of environmental factors in the conidiation of the predacious rotiferovorous fungus Zoophagus insidians (Zoopagomycota)9
Effects of the endophyte Epichloë coenophiala on the root microbial community and growth performance of tall fescue in different saline-alkali soils9
ITS alchemy: On the use of ITS as a DNA marker in fungal ecology9
Highly heterogeneous mycobiota shape fungal diversity in two globally distributed lichens8
Strong climatic effects on ectomycorrhizal fungal communities at seedling establishment stage in ice-age relict forests8
Secondary metabolites and their impact on symbiotic interactions in the ambrosia fungus Geosmithia eupagioceri8
Host-specificity of moss-associated fungal communities in the Ny-Ålesund region (Svalbard, High Arctic) as revealed by amplicon pyrosequencing7
Ericoid mycorrhizal colonization and associated fungal communities along a wetland gradient in the Acadian forest of Eastern Canada7
Six years later: Ectomycorrhizal fungal communities recovering after the end of long-term nitrogen and sulfur addition in a mixed-species temperate North American forest7
Habitat matters: The role of spore bank fungi in early seedling establishment of Florida slash pines7
Truffles in the sky: The impact of stochastic and deterministic drivers on Rhizopogon communities of the Madrean sky island archipelago7
Editorial board7
Evenness modulates effects of the loss of plant litter from rare species on fungal decomposers in tropical streams7
Differences in spore size and atmospheric survival shape stark contrasts in the dispersal dynamics of two closely related fungal pathogens7
Editorial Board7
The response of lichens inhabiting exposed wood of spruce logs to post-hurricane disturbances in Western Carpathian forests7
The emergence of fungal ethology as a distinctive discipline in mycology7
Metabolic activity on Biolog FF MicroPlate suggests organic substrate decomposition by Aspergillus terreus NTOU4989 isolated from Kueishan Island Hydrothermal Vent Field, Taiwan7
The balance between accumulation and loss of soil organic matter in subarctic forest is related to ratios of saprotrophic, ecto- and ericoid mycorrhizal fungal guilds7
Beetles provide directed dispersal of viable spores of a keystone wood decay fungus7
Wood-decay type and fungal guild dominance across a North American log transplant experiment7
Editorial board6
Enhancing repository fungal data for biogeographic analyses6
Temperature sensitivity of soil-borne fungal phytopathogens depends on niche breadth and land use types6
Hidden diversity within Beauveria and Metarhizium – Comparing morphology, barcoding, multilocus phylogenies and whole-genome sequences6
Nitrogen deposition and temperature structure fungal communities associated with alpine moss-sedge heath in the UK6
The potential saprotrophic capacity of foliar endophytic fungi from Quercus gambelii6
Soil microbial and chemical responses to foliar Epichloë fungal infection in Lolium perenne, Hordeum brevisubulatum and Achnatherum inebrians6
Oomycetes associated with Prunus serotina persist in soil after tree harvest6
Endophytes dominate fungal communities in six-year-old veteranisation wounds in living oak trunks6
Editorial board6
Spatiotemporal distribution and dynamic changes of myxomycetes in subtropical forests of China6
Ascospore morphology of bryophilous Pezizales is closely associated with the place of infection and host ecology6
In depth review of the ecology of arenicolous marine fungi5
Flow-network adaptation and behavior in slime molds5
Morchella galilaea – Expanded phylogeography and relaxed seasonality of a globally distributed autumnal morel5
Bidirectional interactions between Grosmannia abietina and hybrid white spruce: Pathogenicity, monoterpene defense responses, and fungal growth and reproduction5
Soil fungal composition changes with shrub encroachment in the northern Chihuahuan Desert5
Climatic shifts threaten alpine mycorrhizal communities above the treeline5
Insights into the functional role of fungi in deep-sea hydrothermal vents through the analysis of stable isotopes of carbon, nitrogen, and sulfur5
Carbon cycling through plant and fungal herbarium specimens tracks the Suess effect over more than a century of environmental change5
Endophytic entomopathogenic fungi isolates as growth promoters of the grass Urochloa brizantha5
Effects of an introduced mustard, Thlaspi arvense, on soil fungal communities in subalpine meadows5
Editorial Board5
DNA metabarcoding reveals compositional and functional differences in fungal communities among Amazonian canga formations5
Microbial community composition unaffected by mycorrhizal plant removal in sub-arctic tundra5
Mr. Toad's wild fungi: Fungal isolate diversity on Colorado boreal toads and their capacity for pathogen inhibition5
Host identity affects the response of mycorrhizal fungal communities to high severity fires in Alaskan boreal forests5
Factors affecting the foliar endophyte community in the invasive weed, Impatiens glandulifera5
Species-specific reliance of trees on ectomycorrhizal fungi for nitrogen supply at an alpine treeline5
The cumulative effects of precipitation determine the occurrence of Tricholoma matsutake fruiting bodies5
Fungus-insect symbiosis: Diversity and negative ecological role of the hypocrealean fungus Trichoderma harzianum in colonies of neotropical termites (Blattodea: Termitidae)4
Revealing the non-overlapping characteristics between original centers and genetic diversity of Purpureocillium lilacinum4
The role and fate of patulin in apple-associated fungal-fungal interactions4
Editorial Board4
Susceptibility of pruning wounds to grapevine trunk disease pathogens Eutypa lata and Diplodia seriata in three climatic conditions in Australia4
Editorial Board4
Nitrogen and phosphorus additions affect fruiting of ectomycorrhizal fungi in a temperate hardwood forest4
Intraspecific interactions among wood-decay fungi alter decay rates and dynamics of interspecific interactions4
Substrate affinities of wood decay fungi are foremost structured by wood properties not climate4
Environmental factors and host genetic variation shape the fungal endophyte communities within needles of Scots pine (Pinus sylvestris)4
Modelling germination and mycelium growth rates of Monostichella coryli under constant temperature conditions4
Does electrical activity in fungi function as a language?4
Lichens as material for Lepidoptera's housing: A molecular approach to a widespread and highly selective interaction4
Editorial Board4
Climate-induced long-term changes in the phenology of Mediterranean fungi4
Global richness of arbuscular mycorrhizal fungi4
Fungal diversity and function in metagenomes sequenced from extreme environments3
Ectomycorrhizal root tips harbor distinctive fungal associates along a soil nitrogen gradient3
The impact of polyphenolic compounds on the in vitro growth of oak-associated foliar endophytic and saprotrophic fungi3
Tracing the spatial extent and lag time of carbon transfer from Picea abies to ectomycorrhizal fungi differing in host type, taxonomy, or hyphal development3
Pine species determine fungal microbiome composition in a common garden experiment3
Fungal endophytes and origins of decay in beech (Fagus sylvatica) sapwood3
Root contact dominates vegetative transmission of the Phialocephala fortinii s.l. – Acephala applanata species complex (PAC)3
Serpula lacrymans reacts with a general, unspecialized chemical response during interaction with mycoparasitic Trichoderma spp. and bacteria3
An exploratory study of species richness and dynamics in the cultivable mycobiota of Palmaria palmata3
Feasibility of active handheld NDVI sensors for monitoring lichen ground cover3
Root and hyphal interactions influence N transfer by arbuscular mycorrhizal fungi in soybean/maize intercropping systems3
Successional changes in fungal communities occur a few weeks following wildfire in a mixed Douglas-fir-ponderosa pine forest3
Diversity and host recurrence of fungi associated with the bleached leaf litter in a subtropical forest3
Deterministic processes have limited impacts on foliar fungal endophyte communities along a savanna-forest successional gradient3
Not always optimal: Fungal fruiting triggers indicate climate sensitivity in cooler regions3
Co-dispersal of symbionts in the lichen Cladonia stellaris inferred from genomic data3
The effects of geographic origin and genotype on fungal diversity of silver birch (Betula pendula)3
Cultivable fungal community associated with the tropical orchid Dichaea andina3
Do aquatic fungal environmental DNA assemblages reflect the surrounding terrestrial sporocarp communities?3
Impact of plant species identity and island characteristics on phyllosphere fungal community structure in an island ecosystem3
Michigan winter wheat (Triticum aestivum L.) roots host communities of Mortierellaceae and endohyphal bacteria3
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