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Yet More “Weeds” in the Garden: Fungal Novelties from Nests of Leaf-Cutting Ants

https://doi.org/10.1371/journal.pone.0082265
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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/jobm.19720120805openalex-snapshot
Pilze aus Pilzgärten von Atta insularis in Kuba
inferredcites →https://doi.org/10.1002/jobm.3630120805openalex-snapshot
Pilze aus Pilzgärten vonAtta insularis in Kuba
inferredcites →https://doi.org/10.1007/978-3-662-10306-7openalex-snapshot
The Ants
inferredcites →https://doi.org/10.1007/s00040-003-0687-zopenalex-snapshot
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inferredcites →https://doi.org/10.1007/s00040-007-0907-zopenalex-snapshot
Fungus garden platforms improve hygiene during nest establishment in Acromyrmex ants (Hymenoptera, Formicidae, Attini)
inferredcites →https://doi.org/10.1007/s00040-010-0137-7openalex-snapshot
A behavioral repertoire of Atta sexdens (Hymenoptera, Formicidae) queens during the claustral founding and ergonomic stages
inferredcites →https://doi.org/10.1007/s00114-007-0262-yopenalex-snapshot
Non-specific association between filamentous bacteria and fungus-growing ants
inferredcites →https://doi.org/10.1007/s00248-008-9380-0openalex-snapshot
Microfungal “Weeds” in the Leafcutter Ant Symbiosis
inferredcites →https://doi.org/10.1007/s00265-010-0936-xopenalex-snapshot
Waste management in the leaf-cutting ant Acromyrmex echinatior: the role of worker size, age and plasticity
inferredcites →https://doi.org/10.1007/s004420100630openalex-snapshot
Prevalence and impact of a virulent parasite on a tripartite mutualism
inferredcites →https://doi.org/10.1007/s10482-008-9268-5openalex-snapshot
Yeasts and filamentous fungi carried by the gynes of leaf-cutting ants
inferredcites →https://doi.org/10.1016/b978-0-12-372180-8.50042-1openalex-snapshot
AMPLIFICATION AND DIRECT SEQUENCING OF FUNGAL RIBOSOMAL RNA GENES FOR PHYLOGENETICS
inferredcites →https://doi.org/10.1016/s0007-1528(83)80051-0openalex-snapshot
Plant Pathologist's Pocketbook
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/10.1017/s0953756201004725openalex-snapshot
The magnitude of fungal diversity: the 1.5 million species estimate revisited
inferredcites →https://doi.org/10.1038/19519openalex-snapshot
Fungus-growing ants use antibiotic-producing bacteria to control garden parasites
inferredcites →https://doi.org/10.1038/ismej.2007.57openalex-snapshot
Labile associations between fungus-growing ant cultivars and their garden pathogens
inferredcites →https://doi.org/10.1038/nature01563openalex-snapshot
Erratum: corrigendum: Fungus-growing ants use antibiotic-producing bacteria to control garden parasites
inferredcites →https://doi.org/10.1073/pnas.0601441103openalex-snapshot
Cryptic sex and many-to-one coevolution in the fungus-growing ant symbiosis
inferredcites →https://doi.org/10.1073/pnas.0711024105openalex-snapshot
Major evolutionary transitions in ant agriculture
inferredcites →https://doi.org/10.1073/pnas.0812082106openalex-snapshot
Candicidin-producing Streptomyces support leaf-cutting ants to protect their fungus garden against the pathogenic fungus Escovopsis
inferredcites →https://doi.org/10.1073/pnas.0904827106openalex-snapshot
Generalized antifungal activity and 454-screening of Pseudonocardia and Amycolatopsis bacteria in nests of fungus-growing ants
inferredcites →https://doi.org/10.1073/pnas.0910004106openalex-snapshot
Rethinking crop-disease management in fungus-growing ants
inferredcites →https://doi.org/10.1073/pnas.95.5.2044openalex-snapshot
Multiple evolutionary origins of the fungus causing Panama disease of banana: Concordant evidence from nuclear and mitochondrial gene genealogies
inferredcites →https://doi.org/10.1073/pnas.96.14.7998openalex-snapshot
The agricultural pathology of ant fungus gardens
inferredcites →https://doi.org/10.1076/0165-0521(200008)35:2;1-9;ft131openalex-snapshot
Leaf-cutting ant nests in temperate environments: mounds, mound damages and nest mortality rate in Acromyrmex lobicornis
inferredcites →https://doi.org/10.1080/00275514.1995.12026546openalex-snapshot
Escovopsis aspergilloides, a rediscovered hyphomycete from leaf-cutting ant nests
inferredcites →https://doi.org/10.1080/00275514.1999.12061051openalex-snapshot
A Method for Designing Primer Sets for Speciation Studies in Filamentous Ascomycetes
inferredcites →https://doi.org/10.1080/08927014.2001.9522772openalex-snapshot
Waste management in leaf-cutting ants
inferredcites →https://doi.org/10.1086/342084openalex-snapshot
Ant versus Fungus versus Mutualism: Ant‐Cultivar Conflict and the Deconstruction of the Attine Ant‐Fungus Symbiosis
inferredcites →https://doi.org/10.1086/652472openalex-snapshot
Comparative Dating of Attine Ant and Lepiotaceous Cultivar Phylogenies Reveals Coevolutionary Synchrony and Discord
inferredcites →https://doi.org/10.1093/bioinformatics/14.9.817openalex-snapshot
MODELTEST: testing the model of DNA substitution.
inferredcites →https://doi.org/10.1093/bioinformatics/btg180openalex-snapshot
MrBayes 3: Bayesian phylogenetic inference under mixed models
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/nar/22.22.4673openalex-snapshot
CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choice
inferredcites →https://doi.org/10.1094/phyto-96-0195openalex-snapshot
Trichoderma : Systematics, the Sexual State, and Ecology
inferredcites →https://doi.org/10.1098/rspb.2001.1605openalex-snapshot
Weeding and grooming of pathogens in agriculture by ants
inferredcites →https://doi.org/10.1098/rspb.2004.2792openalex-snapshot
Exploiting a mutualism: parasite specialization on cultivars within the fungus–growing ant symbiosis
inferredcites →https://doi.org/10.1098/rspb.2007.0431openalex-snapshot
Low host–pathogen specificity in the leaf-cutting ant–microbe symbiosis
inferredcites →https://doi.org/10.1098/rspb.2009.0184openalex-snapshot
Reduced biological control and enhanced chemical pest management in the evolution of fungus farming in ants
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.1365-294x.2007.03225.xopenalex-snapshot
Phylogenetic evidence for an animal pathogen origin of ergot and the grass endophytes
inferredcites →https://doi.org/10.1111/j.1365-294x.2012.05574.xopenalex-snapshot
Molecular phylogenies reveal host‐specific divergence of Ophiocordyceps unilateralis sensu lato following its host ants
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.1119744openalex-snapshot
Coevolved Crypts and Exocrine Glands Support Mutualistic Bacteria in Fungus-Growing Ants
inferredcites →https://doi.org/10.1126/science.1206360openalex-snapshot
Running with the Red Queen: Host-Parasite Coevolution Selects for Biparental Sex
inferredcites →https://doi.org/10.1126/science.1209420openalex-snapshot
Sex, Death, and the Red Queen
inferredcites →https://doi.org/10.1126/science.153.3736.587openalex-snapshot
Fungus-Growing Ants
inferredcites →https://doi.org/10.1186/1471-2148-6-88openalex-snapshot
Complex host-pathogen coevolution in the Apterostigma fungus-growing ant-microbe symbiosis.
inferredcites →https://doi.org/10.1186/1741-7007-8-109openalex-snapshot
A mixed community of actinomycetes produce multiple antibiotics for the fungus farming ant Acromyrmex octospinosus
inferredcites →https://doi.org/10.13102/sociobiology.v60i2.150-153openalex-snapshot
Toxicity of Hydramethylnon to Leaf-cutting Ant Atta sexdens rubropilosa Forel (Hymenoptera: Formicidae)
inferredcites →https://doi.org/10.1371/journal.pbio.0040235openalex-snapshot
Ancient Host–Pathogen Associations Maintained by Specificity of Chemotaxis and Antibiosis
inferredcites →https://doi.org/10.1371/journal.pbio.1001127openalex-snapshot
How Many Species Are There on Earth and in the Ocean?
inferredcites →https://doi.org/10.1371/journal.pbio.1001130openalex-snapshot
Why Worry about How Many Species and Their Loss?
inferredcites →https://doi.org/10.1371/journal.pone.0017024openalex-snapshot
Hidden Diversity Behind the Zombie-Ant Fungus Ophiocordyceps unilateralis: Four New Species Described from Carpenter Ants in Minas Gerais, Brazil
inferredcites →https://doi.org/10.1603/022.038.0110openalex-snapshot
Insect Symbioses: A Case Study of Past, Present, and Future Fungus-growing Ant Research
inferredcites →https://doi.org/10.1603/en09137openalex-snapshot
Presence of Multiparasite Infections Within Individual Colonies of Leaf-Cutter Ants
inferredcites →https://doi.org/10.1890/07-0815.1openalex-snapshot
BLACK YEAST SYMBIONTS COMPROMISE THE EFFICIENCY OF ANTIBIOTIC DEFENSES IN FUNGUS‐GROWING ANTS
inferredcites →https://doi.org/10.2307/3760838openalex-snapshot
Escovopsis aspergilloides, a Rediscovered Hyphomycete from Leaf-Cutting Ant Nests
inferredcites →https://doi.org/10.2307/3762079openalex-snapshot
Pathogenicity of Escovopsis weberi: The Parasite of the Attine Ant-Microbe Symbiosis Directly Consumes the Ant-Cultivated Fungus
inferredcites →https://doi.org/10.3114/sim.2007.57.01openalex-snapshot
Phylogenetic classification of Cordyceps and the clavicipitaceous fungi
inferredcites →https://doi.org/10.3732/ajb.1000298openalex-snapshot
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inferredcites →https://doi.org/10.3852/10-078openalex-snapshot
Trichoderma amazonicum, a new endophytic species on Hevea brasiliensis and H. guianensis from the Amazon basin
inferredcites →https://doi.org/10.3897/phytokeys.6.1960openalex-snapshot
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inferredcites →https://doi.org/10.4161/cib.16721openalex-snapshot
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inferredcites →https://doi.org/10.4161/cib.23095openalex-snapshot
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inferredcites →https://doi.org/10.5248/117.509openalex-snapshot
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inferredcites →https://doi.org/10.5598/imafungus.2011.02.02.06openalex-snapshot
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inferredcites →https://doi.org/10.5962/bhl.title.13146openalex-snapshot
Botanische Mittheilungen aus den Tropen

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.17.182573zenodo-depositor-declared
More diverse than previously thought: a novel Hypocreaceae symbiont from Apterostigma fungus-farming ants
inferred← citeshttps://doi.org/10.1002/9781118958308.ch20openalex-snapshot
Fungal molecular taxonomy
inferred← citeshttps://doi.org/10.1002/9783527686063.ch16openalex-snapshot
Plant‐Animal Dialogues
inferred← citeshttps://doi.org/10.1002/arch.22041openalex-snapshot
Three cuticular amides in the tripartite symbiosis of leafcutter ants
inferred← citeshttps://doi.org/10.1002/ece3.11628openalex-snapshot
Extreme specificity in obligate mutualism—A role for competition?
inferred← citeshttps://doi.org/10.1002/ece3.7379openalex-snapshot
Disease management in two sympatric Apterostigma fungus‐growing ants for controlling the parasitic fungus Escovopsis
inferred← citeshttps://doi.org/10.1007/978-3-319-29532-9_12openalex-snapshot
12 Ecological Genomics of Mycotrophic Fungi
inferred← citeshttps://doi.org/10.1007/978-3-662-65075-2_2openalex-snapshot
Die Ständerpilze (Basidiomycota)
inferred← citeshttps://doi.org/10.1007/s00040-020-00772-7openalex-snapshot
The best of heavy queens: influence of post-flight weight on queens’ survival and productivity in Acromyrmex subterraneus (Forel, 1893) (Hymenoptera: Formicidae)
inferred← citeshttps://doi.org/10.1007/s00248-017-1124-6openalex-snapshot
Symbiont-Mediated Host-Parasite Dynamics in a Fungus-Gardening Ant
inferred← citeshttps://doi.org/10.1007/s10482-014-0367-1openalex-snapshot
Escovopsis trichodermoides sp. nov., isolated from a nest of the lower attine ant Mycocepurus goeldii
inferred← citeshttps://doi.org/10.1007/s10482-016-0666-9openalex-snapshot
Unraveling Trichoderma species in the attine ant environment: description of three new taxa
inferred← citeshttps://doi.org/10.1007/s10482-016-0826-yopenalex-snapshot
Nature of the interactions between hypocrealean fungi and the mutualistic fungus of leaf-cutter ants
inferred← citeshttps://doi.org/10.1007/s11829-014-9329-9openalex-snapshot
Quality control by leaf-cutting ants: evidence from communities of endophytic fungi in foraged and rejected vegetation
inferred← citeshttps://doi.org/10.1007/s13225-015-0331-zopenalex-snapshot
Towards a natural classification and backbone tree for Sordariomycetes
inferred← citeshttps://doi.org/10.1007/s13225-025-00561-2openalex-snapshot
Notes, outline, systematics and phylogeny of hyaline-spored hyphomycetes
inferred← citeshttps://doi.org/10.1007/s43450-023-00417-3openalex-snapshot
Ants/Nest-Associated Fungi and Their Specialized Metabolites: Taxonomy, Chemistry, and Bioactivity
inferred← citeshttps://doi.org/10.1016/j.funbio.2015.09.001openalex-snapshot
Fungal communities in gardens of the leafcutter ant Atta cephalotes in forest and cabruca agrosystems of southern Bahia State (Brazil)
inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100986openalex-snapshot
In vitro study of volatile organic compounds produced by the mutualistic fungus of leaf-cutter ants and the antagonist Escovopsis
inferred← citeshttps://doi.org/10.1016/j.funeco.2022.101140openalex-snapshot
Escovopsioides nivea is a non-specific antagonistic symbiont of ant-fungal crops
inferred← citeshttps://doi.org/10.1016/j.jip.2015.07.008openalex-snapshot
Purpureocillium lilacinum, potential agent for biological control of the leaf-cutting ant Acromyrmex lundii
inferred← citeshttps://doi.org/10.1016/j.myc.2017.04.005openalex-snapshot
Phylogenetic position of Pseudohypocrea (Hypocreales)
inferred← citeshttps://doi.org/10.1038/s42003-025-08654-zopenalex-snapshot
Digging into the evolutionary history of the fungus-growing-ant symbiont, Escovopsis (Hypocreaceae)
inferred← citeshttps://doi.org/10.1073/pnas.2213096119openalex-snapshot
Genomic diversification of the specialized parasite of the fungus-growing ant symbiosis
inferred← citeshttps://doi.org/10.1080/03946975.2019.1603622openalex-snapshot
Variation in nest morphology, queen oviposition rates, and fungal species present in incipient colonies of the leaf-cutter antAtta sexdens
inferred← citeshttps://doi.org/10.1086/686911openalex-snapshot
Patterns of Specificity of the Pathogen Escovopsis across the Fungus-Growing Ant Symbiosis
inferred← citeshttps://doi.org/10.1093/aesa/saag029openalex-snapshot
An entangled bank of species interactions underlies the ecology and evolution of ant fungal agriculture
inferred← citeshttps://doi.org/10.1093/gbe/evag160openalex-snapshot
Evidence for Cryptic Sex in Escovopsis , a Mycoparasite in the Fungus-Growing Ant Symbiosis
inferred← citeshttps://doi.org/10.1098/rsos.150257openalex-snapshot
Shared Escovopsis parasites between leaf-cutting and non-leaf-cutting ants in the higher attine fungus-growing ant symbiosis
inferred← citeshttps://doi.org/10.1098/rsos.161013openalex-snapshot
Putting the waste out: a proposed mechanism for transmission of the mycoparasite Escovopsis between leafcutter ant colonies
inferred← citeshttps://doi.org/10.1098/rspb.2016.0625openalex-snapshot
Social life and sanitary risks: evolutionary and current ecological conditions determine waste management in leaf-cutting ants
inferred← citeshttps://doi.org/10.1111/eea.13078openalex-snapshot
Biological control of leaf‐cutter ants using pathogenic fungi: experimental laboratory and field studies
inferred← citeshttps://doi.org/10.1111/mec.14588openalex-snapshot
Phylogenetic patterns of ant–fungus associations indicate that farming strategies, not only a superior fungal cultivar, explain the ecological success of leafcutter ants
inferred← citeshttps://doi.org/10.1186/s12866-018-1265-xopenalex-snapshot
Escovopsioides as a fungal antagonist of the fungus cultivated by leafcutter ants
inferred← citeshttps://doi.org/10.1186/s43008-021-00078-8openalex-snapshot
Fungi inhabiting attine ant colonies: reassessment of the genus Escovopsis and description of Luteomyces and Sympodiorosea gens. nov.
inferred← citeshttps://doi.org/10.1371/journal.pone.0112067openalex-snapshot
New Light on the Systematics of Fungi Associated with Attine Ant Gardens and the Description of Escovopsis kreiselii sp. nov.
inferred← citeshttps://doi.org/10.22201/ib.20078706e.2020.91.2581openalex-snapshot
Aislamiento y caracterización morfológica y molecular de cepas de Escovopsis aisladas de nidos de hormigas cortadoras de hojas de Argentina
inferred← citeshttps://doi.org/10.3114/sim.2023.106.06openalex-snapshot
Taxonomy and systematics of the fungus-growing ant associate Escovopsis (Hypocreaceae)
inferred← citeshttps://doi.org/10.3389/ffunb.2024.1486601openalex-snapshot
The fungus Escovopsis (Ascomycota: Hypocreales): a critical review of its biology and parasitism of attine ant colonies
inferred← citeshttps://doi.org/10.3389/fmicb.2021.673445openalex-snapshot
Low Virulence of the Fungi Escovopsis and Escovopsioides to a Leaf-Cutting Ant-Fungus Symbiosis
inferred← citeshttps://doi.org/10.3390/agriculture15060642openalex-snapshot
Investigating the Biology of Leaf-Cutting Ants to Support the Development of Alternative Methods for the Control and Management of These Agricultural Pests
inferred← citeshttps://doi.org/10.3390/jof7121007openalex-snapshot
Interactions among Escovopsis, Antagonistic Microfungi Associated with the Fungus-Growing Ant Symbiosis
inferred← citeshttps://doi.org/10.3767/003158517x693417openalex-snapshot
Riding with the ants
inferred← citeshttps://doi.org/10.3897/mycokeys.46.30951openalex-snapshot
More pieces to a huge puzzle: Two new Escovopsis species from fungus gardens of attine ants
inferred← citeshttps://doi.org/10.5248/133.569openalex-snapshot
Five new Escovopsis species from Argentina
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