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Pseudodidymella fagi and Petrakia deviata: Two closely related tree pathogens new to central Europe
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/bf02464386openalex-snapshot
Mycopappus quercus sp. nov., causing frosty mildew in Quercus acutissima
inferredcites →https://doi.org/10.1007/s00248-014-0545-8openalex-snapshot
Forest Health in a Changing World
inferredcites →https://doi.org/10.1007/s10267-006-0319-3openalex-snapshot
First report of Mycopappus alni in Japan: species identification of the pathogenic fungus of a frosty mildew disease in Crataegus chlorosarca
inferredcites →https://doi.org/10.1007/s11056-009-9137-8openalex-snapshot
Ectomycorrhizal communities within beech (Fagus sylvatica L.) forests that naturally regenerate from clear-cutting in northern Spain
inferredcites →https://doi.org/10.1007/s11557-012-0850-xopenalex-snapshot
The complete life cycle of Petrakia echinata
inferredcites →https://doi.org/10.1007/s13225-013-0222-0openalex-snapshot
Leaf-inhabiting endophytic fungi of European Beech (Fagus sylvatica L.) co-occur in leaf litter but are rare on decaying wood of the same host
inferredcites →https://doi.org/10.1007/s13225-016-0366-9openalex-snapshot
Fungal diversity notes 253–366: taxonomic and phylogenetic contributions to fungal taxa
inferredcites →https://doi.org/10.1016/0968-0004(90)90252-7openalex-snapshot
PCR protocols — A guide to methods and applications
inferredcites →https://doi.org/10.1016/j.biocon.2006.02.004openalex-snapshot
Diversity of dead wood inhabiting fungi and bryophytes in semi-natural beech forests in Europe
inferredcites →https://doi.org/10.1016/j.fgb.2004.03.004openalex-snapshot
Evidence for subdivision of the root-endophyte Phialocephala fortinii into cryptic species and recombination within species
inferredcites →https://doi.org/10.1016/j.funeco.2015.12.009openalex-snapshot
A cost-effective and efficient strategy for Illumina sequencing of fungal communities: A case study of beech endophytes identified elevation as main explanatory factor for diversity and community composition
inferredcites →https://doi.org/10.1016/j.tree.2007.04.005openalex-snapshot
The fungal dimension of biological invasions
inferredcites →https://doi.org/10.1017/s0269915x05004052openalex-snapshot
Involvement of Phytophthora species in the decline of European beech in Europe and the USA
inferredcites →https://doi.org/10.1017/s0953756202006779openalex-snapshot
Endophytic mycobiota in bark of European beech (Fagus sylvatica) in the Apennines
inferredcites →https://doi.org/10.1073/pnas.0607968104openalex-snapshot
Phylogenetic signal in plant pathogen–host range
inferredcites →https://doi.org/10.1079/9781780640938.0146openalex-snapshot
The impact of invasive Phytophthora species on European forests.
inferredcites →https://doi.org/10.1079/pavsnnr201510035openalex-snapshot
Plant pathogen evolution and climate change.
inferredcites →https://doi.org/10.1080/00275514.1998.12026915openalex-snapshot
Mycodidymella aesculi gen. et sp. nov. and its synanamorphs Blastostroma aesculi gen. et sp. nov. and Mycopappus aesculi sp. nov. on Aesculus turbinata in Japan
inferredcites →https://doi.org/10.1080/10635150802422282openalex-snapshot
Rooting and Dating Maples (Acer) with an Uncorrelated-Rates Molecular Clock: Implications for North American/Asian Disjunctions
inferredcites →https://doi.org/10.1093/bioinformatics/bts199openalex-snapshot
Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb00479.xopenalex-snapshot
A RECONCILIATION ANALYSIS OF HOST SWITCHING IN PLANT-FUNGAL SYMBIOSES
inferredcites →https://doi.org/10.1111/j.1365-2745.2012.02017.xopenalex-snapshot
Biological F lora of the B ritish I sles: F agus sylvatica
inferredcites →https://doi.org/10.1111/j.1365-294x.1993.tb00005.xopenalex-snapshot
ITS primers with enhanced specificity for basidiomycetes ‐ application to the identification of mycorrhizae and rusts
inferredcites →https://doi.org/10.1111/j.1420-9101.2009.01878.xopenalex-snapshot
Phylogenetic determinants of potential host shifts in fungal pathogens
inferredcites →https://doi.org/10.1111/j.1438-8677.1968.tb00076.xopenalex-snapshot
PETRAKIA IRREGULARIS, A NEW FUNGUS SPECIES
inferredcites →https://doi.org/10.1111/j.1439-0329.1987.tb01119.xopenalex-snapshot
Endophytische Pilze in Blättern und Ästen gesunder und geschädigter Buchen (Fagus sylvatica L.)
inferredcites →https://doi.org/10.1111/j.1469-8137.2012.04364.xopenalex-snapshot
Biogeographical patterns and determinants of invasion by forest pathogens in Europe
inferredcites →https://doi.org/10.1111/mpp.12071openalex-snapshot
Chaperones of the endoplasmic reticulum are required for Ve1 ‐mediated resistance to V erticillium
inferredcites →https://doi.org/10.1111/mpp.12073openalex-snapshot
H ymenoscyphus pseudoalbidus , the causal agent of E uropean ash dieback
inferredcites →https://doi.org/10.1111/mpp.12542openalex-snapshot
Cryphonectria parasitica , the causal agent of chestnut blight: invasion history, population biology and disease control
inferredcites →https://doi.org/10.1139/b85-198openalex-snapshot
Mycopappus, a new genus of leaf pathogens, and two parasitic Anguillospora species
inferredcites →https://doi.org/10.1139/b88-048openalex-snapshot
Mycosphaerella mycopappi sp.aov. and its anamorphs on leaves of Acer macrophyllum
inferredcites →https://doi.org/10.1146/annurev-arplant-043014-115540openalex-snapshot
Responses of Temperate Forest Productivity to Insect and Pathogen Disturbances
inferredcites →https://doi.org/10.1371/journal.pone.0152878openalex-snapshot
Diversity and Composition of the Leaf Mycobiome of Beech (Fagus sylvatica) Are Affected by Local Habitat Conditions and Leaf Biochemistry
inferredcites →https://doi.org/10.2307/3761043openalex-snapshot
Pseudodidymella fagi gen. et sp. nov. and Its Hyphomycete Anamorph Pycnopleiospora fagi gen. et sp. nov. on Fagus crenata in Japan
inferredcites →https://doi.org/10.2307/3761311openalex-snapshot
Mycodidymella aesculi gen. et sp. nov. and Its Synanamorphs Blastostroma aesculi Gen. et sp. nov. and Mycopappus aesculi sp. nov. on Aesculus turbinata in Japan
inferredcites →https://doi.org/10.3100/1043-4534(2006)11[101:poaasb]2.0.co;2openalex-snapshot
PHYLOGENETICS OF ACER (ACEROIDEAE, SAPINDACEAE) BASED ON NUCLEOTIDE SEQUENCES OF TWO CHLOROPLAST NON-CODING REGIONS
inferredcites →https://doi.org/10.3767/003158509x461701openalex-snapshot
Phylogeny and taxonomy of obscure genera of microfungi
inferredcites →https://doi.org/10.3832/ifor1231-008openalex-snapshot
Dutch elm disease and elm bark beetles: a century of association
inferredcites →https://doi.org/10.3897/mycokeys.20.11265openalex-snapshot
What do we learn from cultures in the omics age? High-throughput sequencing and cultivation of leaf-inhabiting endophytes from beech (Fagus sylvatica L.) revealed complementary community composition but similar correlations with local habitat conditions
inferredcites →https://doi.org/10.5598/imafungus.2014.05.01.11openalex-snapshot
Recommendations on generic names competing for use in Leotiomycetes (Ascomycota)
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.11646/phytotaxa.705.1.3zenodo-depositor-declared
Byssosphaeria vaginata, a new species of Melanommataceae from Magnolia officinalis in Sichuan Province, China
inferred← citeshttps://doi.org/10.3897/mycokeys.106.125044zenodo-depositor-declared
An overview of Melanommataceae (Pleosporales, Dothideomycetes): Current insight into the host associations and geographical distribution with some interesting novel additions from plant litter
inferred← citeshttps://doi.org/10.1007/s11557-020-01567-7openalex-snapshot
Phylogenetic revision of Petrakia and Seifertia (Melanommataceae, Pleosporales): new and rediscovered species from Europe and North America
inferred← citeshttps://doi.org/10.1016/j.simyco.2017.07.002openalex-snapshot
Pseudodidymellaceaefam. nov.: Phylogenetic affiliations of mycopappus-like genera inDothideomycetes
inferred← citeshttps://doi.org/10.1038/s43705-021-00004-4openalex-snapshot
Insect herbivory facilitates the establishment of an invasive plant pathogen
inferred← citeshttps://doi.org/10.1111/efp.12452openalex-snapshot
Collapsimycopappus: A new leaf pathogen with mycopappus‐like propagules in Mycosphaerellaceae
inferred← citeshttps://doi.org/10.1111/efp.12479openalex-snapshot
Pseudodidymella fagi in Slovakia: First detection, morphology and culture characteristics
inferred← citeshttps://doi.org/10.3390/f10090718openalex-snapshot
Pseudodidymella fagi in Slovenia: First Report and Expansion of Host Range
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