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Cophylogeny and biogeography of the fungal parasite Cyttaria and its host Nothofagus, southern beech
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1006/clad.2000.0146openalex-snapshot
Nothofagus Biogeography Revisited with Special Emphasis on the Enigmatic Distribution of Subgenus Brassospora in New Caledonia
inferredcites →https://doi.org/10.1007/bf02506808openalex-snapshot
Molecular phylogeny ofNothofagus (Nothofagaceae) based on theatpB-rbcL intergenic spacer of the chloroplast DNA
inferredcites →https://doi.org/10.1016/j.jbi.2005.08.006openalex-snapshot
Traversing the tangle: Algorithms and applications for cophylogenetic studies
inferredcites →https://doi.org/10.1016/s0169-5347(02)02590-9openalex-snapshot
Plant dispersal N.E.W.S from New Zealand
inferredcites →https://doi.org/10.1017/cbo9781139103831openalex-snapshot
Journal of Researches into the Natural History and Geology of the Countries Visited during the Voyage of HMS Beagle round the World, under the Command of Capt. Fitz Roy, R.N.
inferredcites →https://doi.org/10.1071/bt00022openalex-snapshot
Can long-distance dispersal be inferred from the New Zealand plant fossil record?
inferredcites →https://doi.org/10.1071/bt00023openalex-snapshot
The breakup history of Gondwana and its impact on pre-Cenozoic floristic provincialism
inferredcites →https://doi.org/10.1071/bt00026openalex-snapshot
Biogeography, evolution and palaeoecology of Nothofagus (Nothofagaceae): the contribution of the fossil record
inferredcites →https://doi.org/10.1071/bt8310077openalex-snapshot
Cyttaria (Cyttariales): Coevolution with Nothofagus, and Evolutionary Relationship to the Boedijnopezizeae (Pezizales, Sarcoscyphaceae)
inferredcites →https://doi.org/10.1071/sb9910127openalex-snapshot
Biogeographic congruence in the South Pacific
inferredcites →https://doi.org/10.1071/sb9930111openalex-snapshot
The evolutionary history of Nothofagus (Nothofagaceae)
inferredcites →https://doi.org/10.1071/sb9930441openalex-snapshot
Using Sequences of rbc L to Study Phylogeny and Biogeography of Nothofagus Species
inferredcites →https://doi.org/10.1073/pnas.95.16.9402openalex-snapshot
Age and rate of diversification of the Hawaiian silversword alliance (Compositae)
inferredcites →https://doi.org/10.1080/10635150252899734openalex-snapshot
A Statistical Test for Host–Parasite Coevolution
inferredcites →https://doi.org/10.1080/10635150490423430openalex-snapshot
Southern Hemisphere Biogeography Inferred by Event-Based Models: Plant versus Animal Patterns
inferredcites →https://doi.org/10.1080/15572536.2006.11832614openalex-snapshot
Dating divergences in the Fungal Tree of Life: review and new analyses
inferredcites →https://doi.org/10.1093/bioinformatics/19.2.301openalex-snapshot
r8s: inferring absolute rates of molecular evolution and divergence times in the absence of a molecular clock
inferredcites →https://doi.org/10.1093/bioinformatics/btm027openalex-snapshot
C opy C at : cophylogenetic analysis tool
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a003974openalex-snapshot
Estimating Absolute Rates of Molecular Evolution and Divergence Times: A Penalized Likelihood Approach
inferredcites →https://doi.org/10.1093/sysbio/40.2.152openalex-snapshot
Historical Biogeography of Southern South America
inferredcites →https://doi.org/10.1098/rspb.2005.3219openalex-snapshot
Not so ancient: the extant crown group of Nothofagus represents a post-Gondwanan radiation
inferredcites →https://doi.org/10.1111/j.1095-8312.2006.00658.xopenalex-snapshot
The importance of looking at small-scale patterns when inferring Gondwanan biogeography: a case study of the centipedeParalamyctes(Chilopoda, Lithobiomorpha, Henicopidae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1991.tb00199.xopenalex-snapshot
A revised infrageneric classification of Nothofagus (Fagaceae)
inferredcites →https://doi.org/10.1111/j.1095-8339.1991.tb00200.xopenalex-snapshot
Tertiary Nothofagus (Fagaceae) macrofossils from Tasmania and Antarctica and their bearing on the evolution of the genus
inferredcites →https://doi.org/10.1111/j.1096-0031.1994.tb00181.xopenalex-snapshot
TESTING SIGNIFICANCE OF INCONGRUENCE
inferredcites →https://doi.org/10.1111/j.1096-0031.1995.tb00002.xopenalex-snapshot
NOTHOFAGUSAND PACIFIC BIOGEOGRAPHY
inferredcites →https://doi.org/10.1111/j.1096-3642.1842.tb00073.xopenalex-snapshot
V. On an edible Fungus from Tierra del Fuego, and an allied Chilian Species.
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01479.xopenalex-snapshot
Panbiogeography of Nothofagus (Nothofagaceae): analysis of the main species massings
inferredcites →https://doi.org/10.1111/j.1365-2699.2006.01655.xopenalex-snapshot
West Wind Drift revisited: testing for directional dispersal in the Southern Hemisphere using event‐based tree fitting
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1371/journal.pbio.0030014openalex-snapshot
Relaxed Molecular Clock Provides Evidence for Long-Distance Dispersal of Nothofagus (Southern Beech)
inferredcites →https://doi.org/10.2307/2395196openalex-snapshot
Historical Biogeography and Earth History: Perspectives for a Future Synthesis
inferredcites →https://doi.org/10.2307/2446156openalex-snapshot
Systematics of Nothofagus (Nothofagaceae) based on rDNA spacer sequences (ITS): taxonomic congruence with morphology and plastid sequences
inferredcites →https://doi.org/10.2307/2846036openalex-snapshot
The New Zealand Flora-Entirely Long-Distance Dispersal?
inferredcites →https://doi.org/10.2307/2992254openalex-snapshot
Historical Biogeography of Southern South America
inferredcites →https://doi.org/10.3852/10-046openalex-snapshot
Phylogeny ofCyttariainferred from nuclear and mitochondrial sequence and morphological data
inferredcites →https://doi.org/10.5962/bhl.title.128554openalex-snapshot
Journal of researches into the natural history and geology of the countries visited during the voyage of H.M.S. "Beagle" round the world
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.146.1.1zenodo-depositor-declared
Revised circumscription of Nothofagus and recognition of the segregate genera Fuscospora, Lophozonia, and Trisyngyne (Nothofagaceae)
inferred← citeshttps://doi.org/10.1002/ece3.6545openalex-snapshot
Lousy grouse: Comparing evolutionary patterns in Alaska galliform lice to understand host evolution and host–parasite interactions
inferred← citeshttps://doi.org/10.1002/ece3.73758openalex-snapshot
Complex History of Organellar Introgression in Nothofagus Trees: Chloroplast and Mitochondrial Capture Facilitated by Natural Selection
inferred← citeshttps://doi.org/10.1002/ecm.70027openalex-snapshot
Co‐phylogenetic constraints on host breadth within an emerging fungal pathogen complex of global concern
inferred← citeshttps://doi.org/10.1007/978-3-319-15615-6_9openalex-snapshot
Link Prediction in Linked Data of Interspecies Interactions Using Hybrid Recommendation Approach
inferred← citeshttps://doi.org/10.1007/978-3-319-56363-3_13openalex-snapshot
Biogeography of the Ectomycorrhizal Mushroom Genus Laccaria
inferred← citeshttps://doi.org/10.1007/978-3-662-46011-5_3openalex-snapshot
3 Pezizomycotina: Sordariomycetes and Leotiomycetes
inferred← citeshttps://doi.org/10.1007/978-94-017-8783-3_21openalex-snapshot
Galls of the Temperate Forest of Southern South America: Argentina and Chile
inferred← citeshttps://doi.org/10.1007/s11557-021-01736-2openalex-snapshot
Multilocus phylogenetic analysis reveals that Cyttariales is a synonym of Helotiales
inferred← citeshttps://doi.org/10.1007/s11557-025-02097-wopenalex-snapshot
Re-examination of the Southern Hemisphere edible genus Cyttaria (Ascomycota, Helotiales) and characterization of two new species from Patagonia
inferred← citeshttps://doi.org/10.1007/s13127-018-0384-4openalex-snapshot
The origin and diversification of the Entorrhizales: deep evolutionary roots but recent speciation with a phylogenetic and phenotypic split between associates of the Cyperaceae and Juncaceae
inferred← citeshttps://doi.org/10.1007/s13225-017-0389-xopenalex-snapshot
DISCOMYCETES: the apothecial representatives of the phylum Ascomycota
inferred← citeshttps://doi.org/10.1007/s13225-019-00418-5openalex-snapshot
One stop shop II: taxonomic update with molecular phylogeny for important phytopathogenic genera: 26–50 (2019)
inferred← citeshttps://doi.org/10.1007/s13225-019-00433-6openalex-snapshot
One stop shop III: taxonomic update with molecular phylogeny for important phytopathogenic genera: 51–75 (2019)
inferred← citeshttps://doi.org/10.1016/b978-0-12-819990-9.00052-4openalex-snapshot
Phylogenetic Advances in Leotiomycetes, an Understudied Clade of Taxonomically and Ecologically Diverse Fungi
inferred← citeshttps://doi.org/10.1016/j.foreco.2021.119295openalex-snapshot
Tree size and crown structure explain the presence of cavities required by wildlife in cool-temperate forests of South America
inferred← citeshttps://doi.org/10.1016/j.funbio.2017.04.006openalex-snapshot
The Gondwanan connection – Southern temperate Amanita lineages and the description of the first sequestrate species from the Americas
inferred← citeshttps://doi.org/10.1016/j.funbio.2025.101656openalex-snapshot
Diversity of Translucidithyrium (Mycosphaerellales, Phaeothecoidiellaceae) in China: Insights into their evolutionary split time and cophylogeny
inferred← citeshttps://doi.org/10.1016/j.funbio.2026.101777openalex-snapshot
Papiliomyces australis sp. nov. (Clavicipitaceae), infecting lepidopteran hepialid larvae in temperate forests of southern Chile
inferred← citeshttps://doi.org/10.1016/j.ijpara.2018.01.007openalex-snapshot
Host and parasite morphology influence congruence between host and parasite phylogenies
inferred← citeshttps://doi.org/10.1016/j.myc.2012.08.004openalex-snapshot
Origin and evolution of the powdery mildews (Ascomycota, Erysiphales)
inferred← citeshttps://doi.org/10.1017/cbo9781139794749.028openalex-snapshot
When is co-phylogeny evidence ofcoevolution?
inferred← citeshttps://doi.org/10.1071/sb16042openalex-snapshot
Track analysis of agaricoid fungi of the Patagonian forests
inferred← citeshttps://doi.org/10.1080/00275514.2018.1438020openalex-snapshot
A closer look at Sporidiobolales: Ubiquitous microbial community members of plant and food biospheres
inferred← citeshttps://doi.org/10.1080/00275514.2021.1940671openalex-snapshot
Species and genera in Aleurodiscus sensu lato as viewed from the Southern Hemisphere
inferred← citeshttps://doi.org/10.1080/00275514.2026.2705588openalex-snapshot
Pseudomitrulaceace, fam. nov., and three new species of Pseudomitrula expand the known diversity of South American earth tongues
inferred← citeshttps://doi.org/10.1093/obo/9780199941728-0125openalex-snapshot
Evolutionary Biogeography of New Zealand
inferred← citeshttps://doi.org/10.1098/rstb.2020.0363openalex-snapshot
Identifying co-phylogenetic hotspots for zoonotic disease
inferred← citeshttps://doi.org/10.1101/2022.03.09.483579openalex-snapshot
ITS-based assessment of Madagascar’s fungal diversity and arrival of ectomycorrhizal fungi to the island
inferred← citeshttps://doi.org/10.1101/457556openalex-snapshot
Detecting spatial dynamics of range expansions with geo-referenced genomewide SNP data and the geographic spectrum of shared alleles
inferred← citeshttps://doi.org/10.1111/aec.12711openalex-snapshot
Vertebrate consumption and dispersal of the Nothofagaceae associated ascomycete Cyttaria
inferred← citeshttps://doi.org/10.1111/brv.12698openalex-snapshot
Speciation across the T ree of L ife
inferred← citeshttps://doi.org/10.1111/btp.13245openalex-snapshot
DNA‐based fungal diversity in Madagascar and arrival of the ectomycorrhizal fungi to the island
inferred← citeshttps://doi.org/10.1111/evo.12374openalex-snapshot
HOST SWITCHING PROMOTES DIVERSITY IN HOST-SPECIALIZED MYCOPARASITIC FUNGI: UNCOUPLED EVOLUTION IN THEBIATOROPSIS-USNEASYSTEM
inferred← citeshttps://doi.org/10.1111/evo.13386openalex-snapshot
Integrating phylogenomic and population genomic patterns in avian lice provides a more complete picture of parasite evolution
inferred← citeshttps://doi.org/10.1111/j.1365-2699.2011.02624.xopenalex-snapshot
Biogeography and diversification of colletid bees (Hymenoptera: Colletidae): emerging patterns from the southern end of the world
inferred← citeshttps://doi.org/10.1111/jse.12643openalex-snapshot
Unravelling evolutionary relationships between epifoliar Meliolaceae and angiosperms
inferred← citeshttps://doi.org/10.1111/mec.15884openalex-snapshot
Sharing and double‐dating in the lichen world
inferred← citeshttps://doi.org/10.1111/nph.12150openalex-snapshot
Cospeciation vs host‐shift speciation: methods for testing, evidence from natural associations and relation to coevolution
inferred← citeshttps://doi.org/10.1111/nph.14366openalex-snapshot
Fungal–algal association patterns in lichen symbiosis linked to macroclimate
inferred← citeshttps://doi.org/10.1111/nph.18365openalex-snapshot
Biogeographic history of a large clade of ectomycorrhizal fungi, the Russulaceae, in the Neotropics and adjacent regions
inferred← citeshttps://doi.org/10.1111/nph.18802openalex-snapshot
Correlated evolution in an ectomycorrhizal host–symbiont system
inferred← citeshttps://doi.org/10.1128/9781555819583.ch14openalex-snapshot
Long-Distance Dispersal of Fungi
inferred← citeshttps://doi.org/10.1128/microbiolspec.funk-0047-2016openalex-snapshot
Long-Distance Dispersal of Fungi
inferred← citeshttps://doi.org/10.1146/annurev-phyto-082718-100034openalex-snapshot
Revisiting the Concept of Host Range of Plant Pathogens
inferred← citeshttps://doi.org/10.1186/1471-2148-11-230openalex-snapshot
Evolutionary history of Serpulaceae (Basidiomycota): molecular phylogeny, historical biogeography and evidence for a single transition of nutritional mode
inferred← citeshttps://doi.org/10.1186/s43008-019-0010-xopenalex-snapshot
Addressing the diversity of Xylodon raduloides complex through integrative taxonomy
inferred← citeshttps://doi.org/10.1201/b11606-2openalex-snapshot
Integrating Morphological and Molecular Data in Fungal Systematics
inferred← citeshttps://doi.org/10.1371/journal.pone.0117096openalex-snapshot
Evidence for Cryptic Speciation in Directly Transmitted Gyrodactylid Parasites of Trinidadian Guppies
inferred← citeshttps://doi.org/10.1371/journal.pone.0205840openalex-snapshot
Phylogeny, biogeography and taxonomic re-assessment of Multifurca (Russulaceae, Russulales) using three-locus data
inferred← citeshttps://doi.org/10.1371/journal.pone.0250422openalex-snapshot
The mitogenome of Phytophthora agathidicida: Evidence for a not so recent arrival of the “kauri killing” Phytophthora in New Zealand
inferred← citeshttps://doi.org/10.1600/036364415x686297openalex-snapshot
Between a Rock and a Hard Place: Applications of the “Molecular Clock” in Systematic Biology
inferred← citeshttps://doi.org/10.3114/fuse.2022.10.10openalex-snapshot
Two new species of Phaeohelotium ( Leotiomycetes : Helotiaceae ) from Chile and their putative ectomycorrhizal status
inferred← citeshttps://doi.org/10.3767/persoonia.2020.44.04openalex-snapshot
Resurrecting the genus Geomorium: Systematic study of fungi in the genera Underwoodia and Gymnohydnotrya (Pezizales) with the description of three new South American species
inferred← citeshttps://doi.org/10.3767/persoonia.2021.47.01openalex-snapshot
Untangling the Lactifluus clarkeae - Lf. flocktoniae (Russulaceae) species complex in Australasia
inferred← citeshttps://doi.org/10.3767/persoonia.2023.47.01openalex-snapshot
Untangling the Lactifluus clarkeae - Lf. flocktoniae(Russulaceae) species complex in Australasia.
inferred← citeshttps://doi.org/10.3852/10-046openalex-snapshot
Phylogeny ofCyttariainferred from nuclear and mitochondrial sequence and morphological data
inferred← citeshttps://doi.org/10.3897/mycokeys.80.64435openalex-snapshot
Brahmaculus gen. nov. (Leotiomycetes, Chlorociboriaceae)
inferred← citeshttps://doi.org/10.4202/app.00493.2018openalex-snapshot
Phylogenetic relationships and time-calibration of the South American fossils and extant species of southern beeches (Nothofagus)
inferred← citeshttps://doi.org/10.5772/55459openalex-snapshot
Parascript, Parasites and Historical Biogeography
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