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Pseudocospeciation of the mycoparasite Cosmospora with their fungal hosts

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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/fedr.4910960117openalex-snapshot
ROSSMAN, AMY Y., The Phragmosporous Species of Nectria and Related Genera. (Calonectria, Ophionectria, Paranectria, Scoleconectria and Trichonectria). Mycological Papers No. 150. 164 S., 54 Fig., 17 Taf. Commonwealth Mycological Institute. Kew, 1983, Preis £12.00
inferredcites →https://doi.org/10.1007/s10267-010-0052-9openalex-snapshot
Mycoparasitism between Squamanita paradoxa and Cystoderma amianthinum (Cystodermateae, Agaricales)
inferredcites →https://doi.org/10.1016/j.fgb.2008.02.001openalex-snapshot
Speciation in fungi
inferredcites →https://doi.org/10.1016/j.funbio.2012.11.007openalex-snapshot
Lichenicolous fungi show population subdivision by host species but do not share population history with their hosts
inferredcites →https://doi.org/10.1016/j.ympev.2009.08.011openalex-snapshot
Evidence for cospeciation events in the host–symbiont system involving crinoids (Echinodermata) and their obligate associates, the myzostomids (Myzostomida, Annelida)
inferredcites →https://doi.org/10.1016/j.ympev.2009.12.015openalex-snapshot
Phylogenetic status of Xylaria subgenus Pseudoxylaria among taxa of the subfamily Xylarioideae (Xylariaceae) and phylogeny of the taxa involved in the subfamily
inferredcites →https://doi.org/10.1016/s0020-7519(01)00199-0openalex-snapshot
Analytical approaches to measuring cospeciation of host and parasites: through a glass, darkly
inferredcites →https://doi.org/10.1016/s0169-5347(97)01243-3openalex-snapshot
Mistletoes as parasites: Host specificity and speciation
inferredcites →https://doi.org/10.1017/s0953756203008542openalex-snapshot
Host-parasite relationships among bolete infecting Hypomyces species
inferredcites →https://doi.org/10.1017/s0953756205002431openalex-snapshot
Host specialization of the mycoparasite Eudarluca caricis and its evolutionary relationship to Ampelomyces
inferredcites →https://doi.org/10.1038/332258a0openalex-snapshot
Phylogenetic trees support the coevolution of parasites and their hosts
inferredcites →https://doi.org/10.1038/360121a0openalex-snapshot
Gene-for-gene coevolution between plants and parasites
inferredcites →https://doi.org/10.1046/j.1440-1703.2001.00442.xopenalex-snapshot
Cospeciation of ants and plants
inferredcites →https://doi.org/10.1071/app9930072aopenalex-snapshot
Book Review - A Synopsis of Nectria subgen. Dialonectria. G.J. Samuels, A.Y. Rossman, R. Lowen and Rogerson, C.T.. I.M.I./CAB International, Wallingford, Oxon, UK.
inferredcites →https://doi.org/10.1080/10635150252899734openalex-snapshot
A Statistical Test for Host–Parasite Coevolution
inferredcites →https://doi.org/10.1080/10635150290069940openalex-snapshot
Preferential Host Switching by Primate Lentiviruses Can Account for Phylogenetic Similarity with the Primate Phylogeny
inferredcites →https://doi.org/10.1080/10635150490265021openalex-snapshot
Clade-Limited Colonization in Brood Parasitic Finches (Vidua spp.)
inferredcites →https://doi.org/10.1080/10635150500221036openalex-snapshot
Comparing Host and Parasite Phylogenies: Gyrodactylus Flatworms Jumping from Goby to Goby
inferredcites →https://doi.org/10.1080/10635150701311370openalex-snapshot
Multiple Cophylogenetic Analyses Reveal Frequent Cospeciation between Pelecaniform Birds and Pectinopygus Lice
inferredcites →https://doi.org/10.1080/10635150802169610openalex-snapshot
Codivergence in Heteromyid Rodents (Rodentia: Heteromyidae) and Their Sucking Lice of the Genus Fahrenholzia (Phthiraptera: Anoplura)
inferredcites →https://doi.org/10.1080/10635150802172184openalex-snapshot
A Novel Test for Host-Symbiont Codivergence Indicates Ancient Origin of Fungal Endophytes in Grasses
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/10.1086/645087openalex-snapshot
Inverse‐Gene‐for‐Gene Infection Genetics and Coevolutionary Dynamics
inferredcites →https://doi.org/10.1093/bioinformatics/btg412openalex-snapshot
APE: Analyses of Phylogenetics and Evolution in R language
inferredcites →https://doi.org/10.1093/bioinformatics/btu033openalex-snapshot
RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies
inferredcites →https://doi.org/10.1093/molbev/msr121openalex-snapshot
MEGA5: Molecular Evolutionary Genetics Analysis Using Maximum Likelihood, Evolutionary Distance, and Maximum Parsimony Methods
inferredcites →https://doi.org/10.1093/molbev/mss020openalex-snapshot
PartitionFinder: Combined Selection of Partitioning Schemes and Substitution Models for Phylogenetic Analyses
inferredcites →https://doi.org/10.1093/molbev/mst010openalex-snapshot
MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability
inferredcites →https://doi.org/10.1093/nar/gkf436openalex-snapshot
MAFFT: a novel method for rapid multiple sequence alignment based on fast Fourier transform
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026341openalex-snapshot
Interkingdom Host Jumping Underground: Phylogenetic Analysis of Entomoparasitic Fungi of the Genus Cordyceps
inferredcites →https://doi.org/10.1093/sysbio/45.2.151openalex-snapshot
Temporal Congruence Revisited: Comparison of Mitochondrial DNA Sequence Divergence in Cospeciating Pocket Gophers and Their Chewing Lice
inferredcites →https://doi.org/10.1098/rspb.2008.0284openalex-snapshot
Phylogeny and geography predict pathogen community similarity in wild primates and humans
inferredcites →https://doi.org/10.1109/ipdps.2011.344openalex-snapshot
Computing the Tree of Life: Leveraging the Power of Desktop and Service Grids
inferredcites →https://doi.org/10.1111/evo.12169openalex-snapshot
EVOLUTION OF HABITAT PREFERENCE AND NUTRITION MODE IN A COSMOPOLITAN FUNGAL GENUS WITH EVIDENCE OF INTERKINGDOM HOST JUMPS AND MAJOR SHIFTS IN ECOLOGY
inferredcites →https://doi.org/10.1111/evo.12374openalex-snapshot
HOST SWITCHING PROMOTES DIVERSITY IN HOST-SPECIALIZED MYCOPARASITIC FUNGI: UNCOUPLED EVOLUTION IN THEBIATOROPSIS-USNEASYSTEM
inferredcites →https://doi.org/10.1111/j.0014-3820.2003.tb00245.xopenalex-snapshot
LINKING COEVOLUTIONARY HISTORY TO ECOLOGICAL PROCESS: DOVES AND LICE
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.1365-294x.2006.03219.xopenalex-snapshot
Cospeciation in the triplex symbiosis of termite gut protists (Pseudotrichonympha spp.), their hosts, and their bacterial endosymbionts
inferredcites →https://doi.org/10.1111/j.1365-294x.2007.03278.xopenalex-snapshot
Host‐specificity and coevolution among pollinating and nonpollinating New World fig wasps
inferredcites →https://doi.org/10.1111/j.1420-9101.2005.00983.xopenalex-snapshot
Cophylogenetic relationships between penguins and their chewing lice
inferredcites →https://doi.org/10.1111/j.1420-9101.2007.01340.xopenalex-snapshot
When can host shifts produce congruent host and parasite phylogenies? A simulation approach
inferredcites →https://doi.org/10.1111/j.1558-5646.1997.tb02428.xopenalex-snapshot
STATISTICAL TESTS OF HOST-PARASITE COSPECIATION
inferredcites →https://doi.org/10.1111/j.1558-5646.2008.00390.xopenalex-snapshot
RAPID SPECIATION FOLLOWING RECENT HOST SHIFTS IN THE PLANT PATHOGENIC FUNGUS RHYNCHOSPORIUM
inferredcites →https://doi.org/10.1111/j.1744-7429.2006.00176.xopenalex-snapshot
Hypocrealean (Hypocreales, Ascomycota) Fungal Diversity in Different Stages of Tropical Forest Succession in Costa Rica1
inferredcites →https://doi.org/10.1111/nph.12150openalex-snapshot
Cospeciation vs host‐shift speciation: methods for testing, evidence from natural associations and relation to coevolution
inferredcites →https://doi.org/10.1126/science.1078155openalex-snapshot
Ancient Tripartite Coevolution in the Attine Ant-Microbe Symbiosis
inferredcites →https://doi.org/10.1126/science.8066445openalex-snapshot
Disparate Rates of Molecular Evolution in Cospeciating Hosts and Parasites
inferredcites →https://doi.org/10.11646/phytotaxa.44.1.1openalex-snapshot
Volutellonectria (Ascomycota, Fungi), a new genus with Volutella anamorphs
inferredcites →https://doi.org/10.1186/1471-2105-11-s1-s60openalex-snapshot
A parameter-adaptive dynamic programming approach for inferring cophylogenies
inferredcites →https://doi.org/10.1186/1741-7007-5-7openalex-snapshot
Pair of lice lost or parasites regained: the evolutionary history of anthropoid primate lice
inferredcites →https://doi.org/10.1186/1748-7188-5-16openalex-snapshot
Jane: a new tool for the cophylogeny reconstruction problem
inferredcites →https://doi.org/10.1371/journal.pbio.0040337openalex-snapshot
Strict Host-Symbiont Cospeciation and Reductive Genome Evolution in Insect Gut Bacteria
inferredcites →https://doi.org/10.1371/journal.pgen.1001319openalex-snapshot
Estimating Divergence Time and Ancestral Effective Population Size of Bornean and Sumatran Orangutan Subspecies Using a Coalescent Hidden Markov Model
inferredcites →https://doi.org/10.1371/journal.pone.0022252openalex-snapshot
Codivergence of Mycoviruses with Their Hosts
inferredcites →https://doi.org/10.1371/journal.pone.0061048openalex-snapshot
PACo: A Novel Procrustes Application to Cophylogenetic Analysis
inferredcites →https://doi.org/10.1644/1545-1542(2004)085<0167:br>2.0.co;2openalex-snapshot
Tangled Trees: Phylogeny, Cospeciation, and Coevolution
inferredcites →https://doi.org/10.2307/2992181openalex-snapshot
Cospeciation in Host-Parasite Assemblages: Comparative Analysis of Rates of Evolution and Timing of Cospeciation Events
inferredcites →https://doi.org/10.3114/sim.2011.68.04openalex-snapshot
An overview of the taxonomy, phylogeny, and typification of nectriaceous fungi in Cosmospora, Acremonium, Fusarium, Stilbella, and Volutella
inferredcites →https://doi.org/10.32614/r.manualsopenalex-snapshot
R: A Language and Environment for Statistical Computing
inferredcites →https://doi.org/10.3852/09-263openalex-snapshot
Chaetopsinectria(Nectriaceae, Hypocreales), a new genus withChaetopsinaanamorphs
inferredcites →https://doi.org/10.3852/12-395openalex-snapshot
Pseudocosmospora , a new genus to accommodate Cosmospora vilior and related species
inferredcites →https://doi.org/10.3852/14-122openalex-snapshot
Systematics of the Cosmospora viliuscula species complex

What points at this work

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

inferred← citeshttps://doi.org/10.3897/mycokeys.113.140446zenodo-depositor-declared
Resin outpourings on conifers are inhabited by more members of Nectriaceae (Hypocreales, Sordariomycetes) than previously thought
inferred← citeshttps://doi.org/10.1002/ece3.7673openalex-snapshot
Great chemistry between us: The link between plant chemical defenses and butterfly evolution
inferred← citeshttps://doi.org/10.1007/s11557-025-02055-6openalex-snapshot
Novel lineages of fungicolous Cordieritidaceae (Helotiales, Leotiomycetes) from southwest China
inferred← citeshttps://doi.org/10.1007/s13225-019-00422-9openalex-snapshot
Fungicolous fungi: terminology, diversity, distribution, evolution, and species checklist
inferred← citeshttps://doi.org/10.1007/s13225-020-00448-4openalex-snapshot
Microfungi associated with Clematis (Ranunculaceae) with an integrated approach to delimiting species boundaries
inferred← citeshttps://doi.org/10.1016/j.ecoenv.2020.110453openalex-snapshot
Fungal community composition change and heavy metal accumulation in response to the long-term application of anaerobically digested slurry in a paddy soil
inferred← citeshttps://doi.org/10.1016/j.funeco.2016.09.002openalex-snapshot
Pestalotiopsis species occur as generalist endophytes in trees of Western Ghats forests of southern India
inferred← citeshttps://doi.org/10.1016/j.ympev.2022.107680openalex-snapshot
To explore strange new worlds – The diversification in Tremella caloplacae was linked to the adaptive radiation of the Teloschistaceae
inferred← citeshttps://doi.org/10.1111/1462-2920.15862openalex-snapshot
The brown root rot fungus Phellinus noxius affects microbial communities in different root‐associated niches of Ficus trees
inferred← citeshttps://doi.org/10.1111/2041-210x.12736openalex-snapshot
paco: implementing Procrustean Approach to Cophylogeny in R
inferred← citeshttps://doi.org/10.1111/brv.12698openalex-snapshot
Speciation across the T ree of L ife
inferred← citeshttps://doi.org/10.1111/evo.13309openalex-snapshot
Detecting ancient codispersals and host shifts by double dating of host and parasite phylogenies: Application in proctophyllodid feather mites associated with passerine birds
inferred← citeshttps://doi.org/10.1111/jeb.14107openalex-snapshot
Strong phylogenetic congruence between Tulasnella fungi and their associated Drakaeinae orchids
inferred← citeshttps://doi.org/10.17503/agrivita.v41i3.1864openalex-snapshot
Evaluation of Cladosporium sp. Mycoparacites as Biocontrol Agents of White Rust Disease on Chrysanthemum
inferred← citeshttps://doi.org/10.17503/agrivita.v44i1.3379openalex-snapshot
Synergistic Action of PGPR and Biofungicide with Active Ingredient of Cladosporium clasporioides to Control White Rust on Chrysanthemum
inferred← citeshttps://doi.org/10.3390/jof8080799openalex-snapshot
Predicting Species Boundaries and Assessing Undescribed Diversity in Pneumocystis, an Obligate Lung Symbiont
inferred← citeshttps://doi.org/10.3390/jof9070764openalex-snapshot
Glucose-6-phosphate 1-Epimerase CrGlu6 Contributes to Development and Biocontrol Efficiency in Clonostachys chloroleuca
inferred← citeshttps://doi.org/10.3390/microorganisms8091321openalex-snapshot
Endophytic Fungi of Olive Tree
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Natural Fungicolous Regulators of Biscogniauxia destructiva sp. nov. That Causes Beech Bark Tarcrust in Southern European (Fagus sylvatica) Forests
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Masters of the manipulator: two new hypocrealean genera, Niveomyces ( Cordycipitaceae ) and Torrubiellomyces ( Ophiocordycipitaceae ), parasitic on the zombie ant fungus Ophiocordyceps camponoti-floridani
inferred← citeshttps://doi.org/10.3832/ifor3830-014openalex-snapshot
Kretzschmaria deusta, a limiting factor for survival and safety of veteran beech trees in Trentino (Alps, Northern Italy)
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