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 2020-11-01 to 2024-11-01.)
ArticleCitations
Endophyte inoculation enhances Ulmus minor resistance to Dutch elm disease33
Can fungal endophytes fast-track plant adaptations to climate change?32
Drivers of total and pathogenic soil-borne fungal communities in grassland plant species32
ITS alchemy: On the use of ITS as a DNA marker in fungal ecology29
Biotic and abiotic determinants of Batrachochytrium dendrobatidis infections in amphibians of the Brazilian Atlantic Forest25
Rhizosphere fungi actively assimilating plant-derived carbon in a grassland soil22
Morphological and molecular characterization, predatory behaviour and effect of organic extracts of four nematophagous fungi from Mexico21
Stand age affects fungal community composition in a Central European temperate forest20
Endophytic fungus improves peanut drought resistance by reassembling the root-dwelling community of arbuscular mycorrhizal fungi18
Grapevine pruning time affects natural wound colonization by wood-invading fungi18
Virulence traits within a community of the fungal entomopathogen Beauveria: Associations with abundance and distribution18
Pine species determine fungal microbiome composition in a common garden experiment17
Thermal response and horizontal transmission of cameroonian isolates of the entomopathogenic fungi Beauveria bassiana and Metarhizium anisopliae – Candidates for microbial controls of the banana root 17
Saprotrophic and ectomycorrhizal fungi exhibit contrasting richness patterns along elevational gradients in cool-temperate montane forests17
Fungal diversity and functionality are driven by soil texture in Taylor Valley, Antarctica17
Fungal endophytes and origins of decay in beech (Fagus sylvatica) sapwood14
Endophytes dominate fungal communities in six-year-old veteranisation wounds in living oak trunks13
Plant community and soil available nutrients drive arbuscular mycorrhizal fungal community shifts during alpine meadow degradation13
Can orchid mycorrhizal fungi be persistently harbored by the plant host?13
Successional development of wood-inhabiting fungi associated with dominant tree species in a natural temperate floodplain forest12
Modelling range dynamics of terricolous lichens of the genus Peltigera in the Alps under a climate change scenario12
Termites host specific fungal communities that differ from those in their ambient environments11
Host phylogeny is the primary determinant of ectomycorrhizal fungal community composition in the permafrost ecosystem of eastern Siberia at a regional scale10
The cooler the better: Increased aquatic hyphomycete diversity in subtropical streams along a neotropical latitudinal gradient10
Deadwood substrate and species-species interactions determine the release of volatile organic compounds by wood-decaying fungi9
Native and non-native mammals disperse exotic ectomycorrhizal fungi at long distances from pine plantations9
A double-edged sword: Amylostereum areolatum odors attract both Sirex noctilio (Hymenoptera: Siricidae) and its parasitoid, Ibalia leucospoides9
Wood-inhabiting fungal communities: Opportunities for integration of empirical and theoretical community ecology9
Canopy throughfall links canopy epiphytes to terrestrial vegetation in pristine conifer forests9
Fairy rings, associated fungi, and assessment of their distribution across environmental variables using GIS8
Diversity, community composition, and bioactivity of cultivable fungal endophytes in saline and dry soils in deserts8
Z-3-Hexenylacetate emissions induced by the endophyte Epichloë occultans at different levels of defoliation during the host plant's life cycle8
Seagrasses, seaweeds and plant debris: An extraordinary reservoir of fungal diversity in the Mediterranean Sea8
Effects of the endophyte Epichloë coenophiala on the root microbial community and growth performance of tall fescue in different saline-alkali soils8
Carbon allocation mediated by arbuscular mycorrhizal fungi alters the soil microbial community under various phosphorus levels8
Ericoid mycorrhizal colonization and associated fungal communities along a wetland gradient in the Acadian forest of Eastern Canada7
Root and hyphal interactions influence N transfer by arbuscular mycorrhizal fungi in soybean/maize intercropping systems7
Relationships between macro-fungal dark diversity and habitat parameters using LiDAR7
Invasive ectomycorrhizal fungi can disperse in the absence of their known vectors7
Interactions between pinewood nematodes and the fungal community of pine trees7
Climate-induced long-term changes in the phenology of Mediterranean fungi7
Wood-decay type and fungal guild dominance across a North American log transplant experiment7
Mycobiota of Eucommia ulmoides bark: Diversity, rare biosphere and core taxa7
Inside Pandora's box: Development of the lethal myrmecopathogenic fungus Pandora formicae within its ant host7
Endophytic fungal community succession in reproductive organs of two olive tree cultivars with contrasting anthracnose susceptibilities6
Ectomycorrhizal root tips harbor distinctive fungal associates along a soil nitrogen gradient6
Endophytic Fusarium spp. affect yield, but can they be a solution for Botrytis control in vineyard production?6
Root-associated community composition and co-occurrence patterns of fungi in wild grapevine6
Low temperature enhances the ability of the termite-egg-mimicking fungus Athelia termitophila to compete against wood-decaying fungi6
Modelling germination and mycelium growth rates of Monostichella coryli under constant temperature conditions6
Besides stem canker severity, oilseed rape host genotype matters for the production of Leptosphaeria maculans fruit bodies6
Culturable root endophyte communities are shaped by both warming and plant host identity in the Rocky Mountains, USA6
In depth review of the ecology of arenicolous marine fungi6
Relationship and genetic structure among autoecious and heteroecious populations of Cronartium pini in northern Fennoscandia6
In vitro study of volatile organic compounds produced by the mutualistic fungus of leaf-cutter ants and the antagonist Escovopsis6
Hyphal exploration strategies and habitat modification of an arbuscular mycorrhizal fungus in microengineered soil chips6
Fungal community composition and diversity in the rhizosphere soils of Argentina (syn. Potentilla) anserina, on the Qinghai Plateau6
Species-specific trade-offs between regrowth and mycorrhizas in the face of defoliation and phosphorus addition6
Distribution and ecological traits of a rare and threatened fungus Hericium flagellum in Poland with the prediction of its potential occurrence in Europe6
Can seed-borne endophytes promote grass invasion by reducing host dependence on mycorrhizas?6
Soil fungal composition changes with shrub encroachment in the northern Chihuahuan Desert6
Where do nivicolous myxomycetes occur? – Modeling the potential worldwide distribution of Physarum albescens6
Epichloë endophyte affects the root colonization pattern of belowground symbionts in a wild grass6
Enhancing repository fungal data for biogeographic analyses6
Restoration of the mycobiome of the endangered Hawaiian mint Phyllostegia kaalaensis increases its resistance to a common powdery mildew6
Linking wood-decay fungal communities to decay rates: Using a long-term experimental manipulation of deadwood and canopy gaps5
Metabolic activity on Biolog FF MicroPlate suggests organic substrate decomposition by Aspergillus terreus NTOU4989 isolated from Kueishan Island Hydrothermal Vent Field, Taiwan5
Natural populations of the entomopathogenic fungus Beauveria bassiana in Chinese forest ecosystems are diverse and reveal equal frequencies of mating types within phylogenetic species5
Spatiotemporal distribution and dynamic changes of myxomycetes in subtropical forests of China5
Human-associated migration of Holarctic Saccharomyces uvarum strains to Patagonia5
Ratio-dependent functional response of two common Cladocera present in farmland ponds to Batrachochytrium dendrobatidis5
Fungal communities associated with acorn woodpeckers and their excavations5
Specific network and phylosymbiosis pattern in endophyte community of coastal halophytes5
Oomycetes associated with Prunus serotina persist in soil after tree harvest5
Diurnal patterns and conidial dynamics of Batkoa major, a generalist entomophthoralean pathogen5
Beetles provide directed dispersal of viable spores of a keystone wood decay fungus5
Genetic admixture increases phenotypic diversity in the nectar yeast Metschnikowia reukaufii5
Deterministic processes have limited impacts on foliar fungal endophyte communities along a savanna-forest successional gradient5
In silico environmental sampling of emerging fungal pathogens via big data analysis5
Soil microbial and chemical responses to foliar Epichloë fungal infection in Lolium perenne, Hordeum brevisubulatum and Achnatherum inebrians5
Environmental factors and host genetic variation shape the fungal endophyte communities within needles of Scots pine (Pinus sylvestris)5
Biodiversity of mycoplankton in the profile of eutrophic lakes with varying water quality4
Spatial and temporal differences in the community structure of endophytic fungi in the carnivorous plant Pinguicula moranensis (Lentibulariaceae)4
Climate change and plant-microbe interactions: Water-availability influences the effective specialization of a fungal pathogen4
Feasibility of active handheld NDVI sensors for monitoring lichen ground cover4
Fire and local factors shape ectomycorrhizal fungal communities associated with Pinus ponderosa in mountains of the Madrean Sky Island Archipelago4
Susceptibility of pruning wounds to grapevine trunk disease pathogens Eutypa lata and Diplodia seriata in three climatic conditions in Australia4
Effect of stand thinning, former land use and individual tree parameters on wood inhabiting fungal community composition in young living Norway spruce4
Leptographium terebrantis inoculation and associated crown symptoms and tree mortality in Pinus taeda4
Land-cover and climate factors contribute to the prevalence of the ectoparasitic fungus Laboulbenia formicarum in its invasive ant host Lasius neglectus4
Seasonal disconnects between saprobic and mycorrhizal sporocarp communities in the Southern Appalachian Mountains4
Ascospore morphology of bryophilous Pezizales is closely associated with the place of infection and host ecology4
Analysis of digitized herbarium records and community science observations provides a glimpse of downy mildew species diversity of North America, reveals potentially undescribed species, and documents4
Fungal diversity living in the root and sporophore of the endemic Korean fern Mankyua chejuense4
The effects of grazing history, soil properties and stand structure on the communities of saprotrophic fungi in wood-pastures4
Host identity affects the response of mycorrhizal fungal communities to high severity fires in Alaskan boreal forests4
Secondary metabolites and nutrients explain fungal community composition in aspen wood4
Malassezia is widespread and has undescribed diversity in the marine environment3
What determines species composition and diversity of hypogeous fungi in the diet of small mammals? A comparison across mammal species, habitat types and seasons in Central European mountains3
The impact of polyphenolic compounds on the in vitro growth of oak-associated foliar endophytic and saprotrophic fungi3
Arbuscular mycorrhizal fungal abundance in elevation belts of the hyperarid Atacama Desert3
Revealing the non-overlapping characteristics between original centers and genetic diversity of Purpureocillium lilacinum3
Fungal communities associated with roots of two closely related Juglandaceae species with a disjunct distribution in the tropics3
Functional traits of epiphytic lichen communities in a Temperate-Mediterranean fragmented landscape: Importance of patch size, tree diameter and summer rainfall3
Impact of Norway spruce pre-degradation stages induced by Gloeophyllum trabeum on fungal and bacterial communities3
Soil fungal communities are compositionally resistant to drought manipulations – Evidence from culture-dependent and culture-independent analyses3
Citizen science data predict high potential for macrofungal refugia outside protected riparian areas3
The potential saprotrophic capacity of foliar endophytic fungi from Quercus gambelii3
Interaction between growth environment and host progeny shape fungal endophytic assemblages in transplanted Fagus sylvatica3
Response of fungal endophyte communities within Andropogon gerardii (Big bluestem) to nutrient addition and herbivore exclusion3
Electrical potentials in the ectomycorrhizal fungus Laccaria bicolor after a rainfall event3
Evaluating the diversity of the enigmatic fungal phylum Cryptomycota across habitats using 18S rRNA metabarcoding3
Co-invading ectomycorrhizal fungal succession in pine-invaded mountain grasslands3
Cultivable fungal community associated with the tropical orchid Dichaea andina3
Polyphyly, asexual reproduction and dual trophic mode in Buchwaldoboletus3
Nitrogen deposition and temperature structure fungal communities associated with alpine moss-sedge heath in the UK3
Host-specificity of moss-associated fungal communities in the Ny-Ålesund region (Svalbard, High Arctic) as revealed by amplicon pyrosequencing3
Lichens as material for Lepidoptera's housing: A molecular approach to a widespread and highly selective interaction3
Does electrical activity in fungi function as a language?3
Laboratory conditions can change the complexity and composition of the natural aquatic mycobiome on Alnus glutinosa leaf litter3
Patterns of community composition and diversity in latent fungi of living Quercus serrata trunks across a range of oak wilt prevalence and climate variables in Japan3
Non-invasive monitoring of photosynthetic activity and water content in forest lichens by spectral reflectance data and RGB colors from photographs3
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