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Austrostigmidium, a new austral genus of lichenicolous fungi close to rock-inhabiting meristematic fungi inTeratosphaeriaceae

https://doi.org/10.1017/s0024282915000031

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/tax.596008openalex-snapshot

Phylogenetic generic classification of parmelioid lichens (Parmeliaceae, Ascomycota) based on molecular, morphological and chemical evidence

inferredcites →https://doi.org/10.1007/3-540-30985-3_20openalex-snapshot

Black Yeasts and Meristematic Fungi: Ecology, Diversity and Identification

inferredcites →https://doi.org/10.1007/978-3-642-56359-1_7openalex-snapshot

Preparative Techniques for Transmission Electron Microscopy and Confocal Laser Scanning Microscopy of Lichens

inferredcites →https://doi.org/10.1007/bf01084401openalex-snapshot

DNA extraction and PCR amplification method suitable for fresh, herbarium-stored, lichenized, and other fungi

inferredcites →https://doi.org/10.1007/s11557-014-0990-2openalex-snapshot

A reappraisal of orders and families within the subclass Chaetothyriomycetidae (Eurotiomycetes, Ascomycota)

inferredcites →https://doi.org/10.1007/s13225-012-0179-4openalex-snapshot

Molecular data place the hyphomycetous lichenicolous genus Sclerococcum close to Dactylospora (Eurotiomycetes) and S. parmeliae in Cladophialophora (Chaetothyriales)

inferredcites →https://doi.org/10.1007/s13225-013-0250-9openalex-snapshot

Molecular data resolve a new order of Arthoniomycetes sister to the primarily lichenized Arthoniales and composed of black yeasts, lichenicolous and rock-inhabiting species

inferredcites →https://doi.org/10.1007/s13225-013-0269-yopenalex-snapshot

Lichenicolous fungi of the genus Abrothallus (Dothideomycetes: Abrothallales ordo nov.) are sister to the predominantly aquatic Janhulales

inferredcites →https://doi.org/10.1007/s13225-013-0277-yopenalex-snapshot

Phylogeny and taxonomy of meristematic rock-inhabiting black fungi in the Dothideomycetes based on multi-locus phylogenies

inferredcites →https://doi.org/10.1007/s13225-014-0287-4openalex-snapshot

Multiple origin of the lichenicolous life habit in Helotiales, based on nuclear ribosomal sequences

inferredcites →https://doi.org/10.1016/j.ympev.2011.05.014openalex-snapshot

Phylogeny and character evolution in the jelly fungi (Tremellomycetes, Basidiomycota, Fungi)

inferredcites →https://doi.org/10.1016/s0024-2829(02)00097-xopenalex-snapshot

Three New Species of Stigmidium s. l. (lichenicolous ascomycetes) on Acarospora and Squamarina

inferredcites →https://doi.org/10.1016/s0953-7562(08)61975-9openalex-snapshot

Observations on Biatoropsis usnearum, a lichenicolous heterobasidiomycete, and other gall-forming lichenicolous fungi, using different microscopical techniques

inferredcites →https://doi.org/10.1016/s0953-7562(09)80409-7openalex-snapshot

Taxonomy and phylogeny of Gliocladium analysed from nuclear large subunit ribosomal DNA sequences

inferredcites →https://doi.org/10.1016/s1055-7903(02)00214-2openalex-snapshot

Phylogeny of the Gyalectales and Ostropales (Ascomycota, Fungi): among and within order relationships based on nuclear ribosomal RNA small and large subunits

inferredcites →https://doi.org/10.1017/s0953756200002951openalex-snapshot

Host-parasite interfaces of some lichenicolous fungi in the Dacampiaceae (Dothideales, Ascomycota)

inferredcites →https://doi.org/10.1017/s0953756205003631openalex-snapshot

Microcolonial rock inhabiting fungi and lichen photobionts: evidence for mutualistic interactions

inferredcites →https://doi.org/10.1017/s0954102006000344openalex-snapshot

Lichenicolous fungi described from Antarctica and the sub-Antarctic islands by Carroll W. Dodge (1895–1988)

inferredcites →https://doi.org/10.1038/nmeth.2109openalex-snapshot

jModelTest 2: more models, new heuristics and parallel computing

inferredcites →https://doi.org/10.1080/10635150802429642openalex-snapshot

A Rapid Bootstrap Algorithm for the RAxML Web Servers

inferredcites →https://doi.org/10.1083/jcb.17.1.208openalex-snapshot

THE USE OF LEAD CITRATE AT HIGH pH AS AN ELECTRON-OPAQUE STAIN IN ELECTRON MICROSCOPY

inferredcites →https://doi.org/10.1093/bioinformatics/btl446openalex-snapshot

RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models

inferredcites →https://doi.org/10.1093/nar/gkh340openalex-snapshot

MUSCLE: multiple sequence alignment with high accuracy and high throughput

inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026334openalex-snapshot

Selection of Conserved Blocks from Multiple Alignments for Their Use in Phylogenetic Analysis

inferredcites →https://doi.org/10.1093/sysbio/sys029openalex-snapshot

MrBayes 3.2: Efficient Bayesian Phylogenetic Inference and Model Choice Across a Large Model Space

inferredcites →https://doi.org/10.1109/gce.2010.5676129openalex-snapshot

Creating the CIPRES Science Gateway for inference of large phylogenetic trees

inferredcites →https://doi.org/10.1111/j.1529-8817.2012.01172.xopenalex-snapshot

MOLECULAR PHYLOGENY OF ANTARCTIC PRASIOLA (PRASIOLALES, TREBOUXIOPHYCEAE) REVEALS EXTENSIVE CRYPTIC DIVERSITY1

inferredcites →https://doi.org/10.1128/jb.172.8.4238-4246.1990openalex-snapshot

Rapid genetic identification and mapping of enzymatically amplified ribosomal DNA from several Cryptococcus species

inferredcites →https://doi.org/10.1139/b96-183openalex-snapshot

Le Clauzadella gordensis gen. et sp. nov., ascomycète lichénicole non lichénisé (Verrucariales, Verrucariaceae)

inferredcites →https://doi.org/10.1214/aos/1176344136openalex-snapshot

Estimating the Dimension of a Model

inferredcites →https://doi.org/10.12705/634.20openalex-snapshot

The Arthonialean challenge: Restructuring Arthoniaceae

inferredcites →https://doi.org/10.14601/phytopathol_mediterr-14998u1.29openalex-snapshot

BIOEDIT: A USER-FRIENDLY BIOLOGICAL SEQUENCE ALIGNMENT EDITOR AND ANALYSIS PROGRAM FOR WINDOWS 95/98/ NT

inferredcites →https://doi.org/10.1639/0007-2745(2003)106[0080:lfieab]2.0.co;2openalex-snapshot

Lichenicolous Fungi: Interactions, Evolution, and Biodiversity

inferredcites →https://doi.org/10.1639/14openalex-snapshot

Lichenicolous Fungi from Central Alaska: New Records and Range Extensions

inferredcites →https://doi.org/10.2307/3243364openalex-snapshot

The Inter-Lecanoralean Associations

inferredcites →https://doi.org/10.3114/sim.2007.58.01openalex-snapshot

Mycosphaerella is polyphyletic

inferredcites →https://doi.org/10.3114/sim.2008.61.11openalex-snapshot

A rock-inhabiting ancestor for mutualistic and pathogen-rich fungal lineages

inferredcites →https://doi.org/10.3114/sim.2009.64.06openalex-snapshot

Phylogeny of rock-inhabiting fungi related to Dothideomycetes

inferredcites →https://doi.org/10.3390/biology2020784openalex-snapshot

Antarctic Epilithic Lichens as Niches for Black Meristematic Fungi

inferredcites →https://doi.org/10.3732/ajb.0900323openalex-snapshot

Symbiotic lifestyle and phylogenetic relationships of the bionts of Mastodia tessellata (Ascomycota, incertae sedis)

inferredcites →https://doi.org/10.5281/zenodo.16004110openalex-snapshot

MOOSBEWOHNENDE ASCOMYCETEN I. DIE PYRENOCARPEN, DEN GAMETOPHYTEN BESIEDELNDEN ARTEN

inferredcites →https://doi.org/10.5598/imafungus.2011.02.01.13openalex-snapshot

Molecular phylogenetic studies on the lichenicolous Xanthoriicola physciae reveal Antarctic rock-inhabiting fungi and Piedraia species among closest relatives in the Teratosphaeriaceae

inferredcites →https://doi.org/10.5962/p.381973openalex-snapshot

Lichenicolous Fungi and some lichens from the Holarctic

inferredcites →https://doi.org/10.5962/p.382007openalex-snapshot

Lichenicolous fungi and lichens growing on Stereocaulon from the Holarctic, with a key to the known species.

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.3897/imafungus.16.175931zenodo-depositor-declared

Novel endophytic fungi from Pinus: introducing three new genera and six new species within Capnodiales (Ascomycota, Dothideomycetes) sensu lato

inferred← citeshttps://doi.org/10.1007/s11557-022-01860-7openalex-snapshot

Taxonomic and phylogenetic approach to some Antarctic lichenicolous fungi

inferred← citeshttps://doi.org/10.1007/s13225-017-0386-0openalex-snapshot

Notes for genera: Ascomycota

inferred← citeshttps://doi.org/10.1017/s002428292000047xopenalex-snapshot

Contributions to the knowledge of lichenicolous fungi growing on baeomycetoid lichens andIcmadophila, with a key to the species

inferred← citeshttps://doi.org/10.1080/00275514.2019.1603500openalex-snapshot

A new genus, Zhurbenkoa , and a novel nutritional mode revealed in the family Malmideaceae (Lecanoromycetes, Ascomycota)

inferred← citeshttps://doi.org/10.13158/heia.29.2.2016.315openalex-snapshot

Lichenicolous Lichens and Fungi from Monfragüe National Park (Western Spain)

inferred← citeshttps://doi.org/10.1639/0007-2745-119.1.107openalex-snapshot

Recent literature on lichens—240

inferred← citeshttps://doi.org/10.1639/0007-2745-121.3.340openalex-snapshot

The 2018 classification and checklist of lichenicolous fungi, with 2000 non-lichenized, obligately lichenicolous taxa

inferred← citeshttps://doi.org/10.1639/0007-2745-128.4.765openalex-snapshot

The 2025 classification and checklist of lichenicolous fungi: documenting a rapidly growing knowledge of diversity

inferred← citeshttps://doi.org/10.3390/app15095149openalex-snapshot

Cell Response to Oxidative Stress in Antarctic Filamentous Fungi

inferred← citeshttps://doi.org/10.3390/jof7030180openalex-snapshot

Insight into the Systematics of Microfungi Colonizing Dead Woody Twigs of Dodonaea viscosa in Honghe (China)

inferred← citeshttps://doi.org/10.3390/jof9040423openalex-snapshot

Fungal Diversity Associated with Thirty-Eight Lichen Species Revealed a New Genus of Endolichenic Fungi, Intumescentia gen. nov. (Teratosphaeriaceae)

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