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Labile associations between fungus-growing ant cultivars and their garden pathogens
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/0470022620.bbc25openalex-snapshot
Analysis of Population Subdivision
inferredcites →https://doi.org/10.1002/0471650129.dob0522openalex-snapshot
PAUP * [Phylogenetic Analysis Using Parsimony (and Other Methods)]
inferredcites →https://doi.org/10.1002/ajhb.10105openalex-snapshot
Parasitism. The ecology and evolution of intimate interactions
inferredcites →https://doi.org/10.1007/s00439-001-0667-1openalex-snapshot
Handbook of statistical genetics:
inferredcites →https://doi.org/10.1007/s004420100630openalex-snapshot
Prevalence and impact of a virulent parasite on a tripartite mutualism
inferredcites →https://doi.org/10.1016/j.pt.2005.08.009openalex-snapshot
Speciation in parasites: a population genetics approach
inferredcites →https://doi.org/10.1016/s0022-2836(83)80320-9openalex-snapshot
Chromosomal walking and jumping to isolate DNA from the Ace and rosy loci and the bithorax complex in Drosophila melanogaster
inferredcites →https://doi.org/10.1016/s0169-5347(03)00223-4openalex-snapshot
Parasite local adaptation: Red Queen versus Suicide King
inferredcites →https://doi.org/10.1016/s0169-5347(98)01358-5openalex-snapshot
Local adaptation and host–parasite interactions
inferredcites →https://doi.org/10.1017/s0031182001007727openalex-snapshot
Parasite (Schistosoma mansoni) and host (Biomphalaria glabrata) genetic diversity: population structure in a fragmented landscape
inferredcites →https://doi.org/10.1017/s0031182099004722openalex-snapshot
Host–parasite population genetics: a cross-sectional comparison of Bulinus globosus and Schistosoma haematobium
inferredcites →https://doi.org/10.1038/35015069openalex-snapshot
Parasite adaptation to locally common host genotypes
inferredcites →https://doi.org/10.1038/nature00810openalex-snapshot
Geographic structure and dynamics of coevolutionary selection
inferredcites →https://doi.org/10.1038/sj.hdy.6800142openalex-snapshot
Population structure of a parasitic plant and its perennial host
inferredcites →https://doi.org/10.1038/sj.hdy.6884350openalex-snapshot
Local adaptation in host–parasite systems
inferredcites →https://doi.org/10.1038/sj.hdy.6884850openalex-snapshot
Host and parasite population structure in a natural plant–pathogen system
inferredcites →https://doi.org/10.1046/j.0962-1083.2002.01462.xopenalex-snapshot
Comparative population structure and genetic diversity of Arceuthobium americanum (Viscaceae) and its Pinus host species: insight into host–parasite evolution in parasitic angiosperms
inferredcites →https://doi.org/10.1046/j.1365-294x.2000.00880.xopenalex-snapshot
Comparative genetic diversity of parasites and their hosts: population structure of an urban cockroach and its haplo‐diploid parasite (oxyuroid nematode)
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01433.xopenalex-snapshot
Extensive exchange of fungal cultivars between sympatric species of fungus‐growing ants
inferredcites →https://doi.org/10.1046/j.1365-294x.2002.01512.xopenalex-snapshot
A Bayesian approach to inferring population structure from dominant markers
inferredcites →https://doi.org/10.1046/j.1420-9101.2000.00226.xopenalex-snapshot
Local adaptation of a holoparasitic plant, Cuscuta europaea: variation among populations
inferredcites →https://doi.org/10.1046/j.1420-9101.2002.00402.xopenalex-snapshot
Local adaptation, evolutionary potential and host–parasite coevolution: interactions between migration, mutation, population size and generation time
inferredcites →https://doi.org/10.1046/j.1570-7458.2003.00077.xopenalex-snapshot
Comparative population genetic structures of the fruit fly Urophora cardui and its primary parasitoid Eurytoma robusta
inferredcites →https://doi.org/10.1073/pnas.0511240103openalex-snapshot
Variable host–pathogen compatibility in Mycobacterium tuberculosis
inferredcites →https://doi.org/10.1073/pnas.0607968104openalex-snapshot
Phylogenetic signal in plant pathogen–host range
inferredcites →https://doi.org/10.1073/pnas.76.10.5269openalex-snapshot
Mathematical model for studying genetic variation in terms of restriction endonucleases.
inferredcites →https://doi.org/10.1073/pnas.96.14.7998openalex-snapshot
The agricultural pathology of ant fungus gardens
inferredcites →https://doi.org/10.1080/00275514.1995.12026546openalex-snapshot
Escovopsis aspergilloides, a rediscovered hyphomycete from leaf-cutting ant nests
inferredcites →https://doi.org/10.1080/15572536.2005.11832895openalex-snapshot
Pathogenicity of Escovopsis weberi : The parasite of the attine ant-microbe symbiosis directly consumes the ant-cultivated fungus
inferredcites →https://doi.org/10.1086/303208openalex-snapshot
Specific Hypotheses on the Geographic Mosaic of Coevolution
inferredcites →https://doi.org/10.1086/303210openalex-snapshot
Migration, Virulence, and the Geographic Mosaic of Adaptation by Parasites
inferredcites →https://doi.org/10.1093/genetics/155.2.945openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data
inferredcites →https://doi.org/10.1093/genetics/164.4.1567openalex-snapshot
Inference of Population Structure Using Multilocus Genotype Data: Linked Loci and Correlated Allele Frequencies
inferredcites →https://doi.org/10.1098/rspb.1996.0148openalex-snapshot
Local adaptation and gene-for-gene coevolution in a metapopulation model
inferredcites →https://doi.org/10.1098/rspb.2004.2759openalex-snapshot
Convergent coevolution in the domestication of coral mushrooms by fungus–growing 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/10.1111/j.0014-3820.2001.tb00633.xopenalex-snapshot
GENETIC VARIATION IN A HOST-PARASITE ASSOCIATION: POTENTIAL FOR COEVOLUTION AND FREQUENCY-DEPENDENT SELECTION
inferredcites →https://doi.org/10.1111/j.0014-3820.2001.tb01315.xopenalex-snapshot
PARTIAL INCOMPATIBILITY BETWEEN ANTS AND SYMBIOTIC FUNGI IN TWO SYMPATRIC SPECIES OF ACROMYRMEX LEAF-CUTTING ANTS
inferredcites →https://doi.org/10.1111/j.0014-3820.2004.tb01601.xopenalex-snapshot
EVOLUTION OF ANT-CULTIVAR SPECIALIZATION AND CULTIVAR SWITCHING IN APTEROSTIGMA FUNGUS-GROWING ANTS
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02553.xopenalex-snapshot
Detecting the number of clusters of individuals using the software structure : a simulation study
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02587.xopenalex-snapshot
Molecular ecology of parasites: elucidating ecological and microevolutionary processes
inferredcites →https://doi.org/10.1111/j.1365-294x.2005.02695.xopenalex-snapshot
Specificity of the mutualistic association between actinomycete bacteria and two sympatric species of Acromyrmex leaf‐cutting ants
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03073.xopenalex-snapshot
Population structure between environmentally transmitted vibrios and bobtail squids using nested clade analysis
inferredcites →https://doi.org/10.1111/j.1365-294x.2006.03134.xopenalex-snapshot
Population genetic signatures of diffuse co‐evolution between leaf‐cutting ants and their cultivar fungi
inferredcites →https://doi.org/10.1111/j.1469-1809.1977.tb01918.xopenalex-snapshot
F ‐statistics and analysis of gene diversity in subdivided populations
inferredcites →https://doi.org/10.1111/j.1558-5646.1985.tb00414.xopenalex-snapshot
LOCAL POPULATION DIFFERENTIATION FOR COMPATIBILITY IN AN ANNUAL LEGUME AND ITS HOST-SPECIFIC FUNGAL PATHOGEN
inferredcites →https://doi.org/10.1111/j.1558-5646.1989.tb02616.xopenalex-snapshot
ADAPTATION BY A PARASITIC TREMATODE TO LOCAL POPULATIONS OF ITS SNAIL HOST
inferredcites →https://doi.org/10.1111/j.1558-5646.1991.tb02668.xopenalex-snapshot
COMPARATIVE POPULATION GENETIC STRUCTURE OF A PARASITE (FASCIOLOIDES MAGNA) AND ITS DEFINITIVE HOST
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb03615.xopenalex-snapshot
THE GEOGRAPHY OF COEVOLUTION: COMPARATIVE POPULATION STRUCTURES FOR A SNAIL AND ITS TREMATODE PARASITE
inferredcites →https://doi.org/10.1111/j.1558-5646.1999.tb05352.xopenalex-snapshot
COMPARATIVE POPULATION STRUCTURE AND GENE FLOW OF A BROOD PARASITE, THE GREAT SPOTTED CUCKOO (CLAMATOR GLANDARIUS), AND ITS PRIMARY HOST, THE MAGPIE (PICA PICA)
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.1106688openalex-snapshot
Mutualistic Fungi Control Crop Diversity in Fungus-Growing Ants
inferredcites →https://doi.org/10.1126/science.266.5191.1691openalex-snapshot
Evolutionary History of the Symbiosis Between Fungus-Growing Ants and Their Fungi
inferredcites →https://doi.org/10.1128/aem.64.9.3209-3213.1998openalex-snapshot
Competitive Dominance among Strains of Luminous Bacteria Provides an Unusual Form of Evidence for Parallel Evolution in Sepiolid Squid-Vibrio Symbioses
inferredcites →https://doi.org/10.1146/annurev.es.16.110185.002141openalex-snapshot
Gene Flow in Natural Populations
inferredcites →https://doi.org/10.1186/1471-2148-4-49openalex-snapshot
Diversity and specificity in the interaction between Caenorhabditis elegans and the pathogen Serratia marcescens
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/10.1371/journal.pbio.0040235openalex-snapshot
Ancient Host–Pathogen Associations Maintained by Specificity of Chemotaxis and Antibiosis
inferredcites →https://doi.org/10.18637/jss.v007.i10openalex-snapshot
zt: A Software Tool for Simple and Partial Mantel Tests
inferredcites →https://doi.org/10.2307/2409784openalex-snapshot
Comparative Population Genetic Structure of a Parasite (Fascioloides magna) and Its Definitive Host
inferredcites →https://doi.org/10.2307/2640939openalex-snapshot
Comparative Population Structure and Gene Flow of a Brood Parasite, The Great Spotted Cuckoo (Clamator glandarius), and Its Primary Host, the Magpie (Pica pica)
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
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.2139/ssrn.4588068openalex-extracted
Exploring the Escovopsis and L. Gongylophorus Interaction: Mycoparasitism and Biocontrol Prospects
inferred← citeshttps://doi.org/10.1007/978-90-481-9316-5_2openalex-snapshot
The Leaf-Cutting Ant–plant Interaction from a Microbial Ecology Perspective
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/s13199-011-0119-1openalex-snapshot
Anthropogenic effects on interaction outcomes: examples from insect-microbial symbioses in forest and savanna ecosystems
inferred← citeshttps://doi.org/10.1016/j.cois.2014.08.004openalex-snapshot
Microbial secondary metabolites and their impacts on insect symbioses
inferred← citeshttps://doi.org/10.1016/j.funeco.2020.100944openalex-snapshot
Lack of fungal cultivar fidelity and low virulence of Escovopsis trichodermoides
inferred← citeshttps://doi.org/10.1016/j.mib.2012.03.001openalex-snapshot
Symbiont recruitment versus ant-symbiont co-evolution in the attine ant–microbe symbiosis
inferred← citeshttps://doi.org/10.1086/667886openalex-snapshot
The Population Structure of Antibiotic-Producing Bacterial Symbionts ofApterostigma dentigerumAnts: Impacts of Coevolution and Multipartite Symbiosis
inferred← citeshttps://doi.org/10.1086/680501openalex-snapshot
The Most Relictual Fungus-Farming Ant Species Cultivates the Most Recently Evolved and Highly Domesticated Fungal Symbiont Species
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/10.1098/rspb.2010.2118openalex-snapshot
Specificity in the symbiotic association between fungus-growing ants and protective Pseudonocardia bacteria
inferred← citeshttps://doi.org/10.1098/rspb.2015.0212openalex-snapshot
Functional role of phenylacetic acid from metapleural gland secretions in controlling fungal pathogens in evolutionarily derived leaf-cutting ants
inferred← citeshttps://doi.org/10.1111/btp.13171openalex-snapshot
Limited genetic differentiation of Mycetomoellerius mikromelanos in Parque National Soberanía, Panama: Implications for queen dispersal
inferred← citeshttps://doi.org/10.1111/j.1558-5646.2008.00501.xopenalex-snapshot
COEVOLUTION BETWEEN ATTINE ANTS AND ACTINOMYCETE BACTERIA: A REEVALUATION
inferred← citeshttps://doi.org/10.1111/j.1758-2229.2009.00098.xopenalex-snapshot
Variation in Pseudonocardia antibiotic defence helps govern parasite‐induced morbidity in Acromyrmex leaf‐cutting ants
inferred← citeshttps://doi.org/10.1111/syen.12289openalex-snapshot
Evolution, systematics, and natural history of a new genus of cryptobiotic fungus‐growing ants
inferred← citeshttps://doi.org/10.1128/aem.01580-19openalex-snapshot
Local Adaptation of Bacterial Symbionts within a Geographic Mosaic of Antibiotic Coevolution
inferred← citeshttps://doi.org/10.1128/msystems.00576-24openalex-snapshot
Genomic insights into the evolution of secondary metabolism of Escovopsis and its allies, specialized fungal symbionts of fungus-farming ants
inferred← citeshttps://doi.org/10.1155/2012/239392openalex-snapshot
Towards a Better Understanding of the Evolution of Specialized Parasites of Fungus-Growing Ant Crops
inferred← citeshttps://doi.org/10.1155/2012/905109openalex-snapshot
Specialized Fungal Parasites and Opportunistic Fungi in Gardens of Attine 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/10.1371/journal.pone.0082265openalex-snapshot
Yet More “Weeds” in the Garden: Fungal Novelties from Nests of Leaf-Cutting Ants
inferred← citeshttps://doi.org/10.1603/022.038.0110openalex-snapshot
Insect Symbioses: A Case Study of Past, Present, and Future Fungus-growing Ant Research
inferred← citeshttps://doi.org/10.1603/en09137openalex-snapshot
Presence of Multiparasite Infections Within Individual Colonies of Leaf-Cutter Ants
inferred← citeshttps://doi.org/10.1603/en10111openalex-snapshot
Growth and Conidiation Response of Escovopsis weberi (Ascomycota: Hypocreales) Against the Fungal Cultivar of Acromyrmex lundii (Hymenoptera: Formicidae)
inferred← citeshttps://doi.org/10.3390/jof7121007openalex-snapshot
Interactions among Escovopsis, Antagonistic Microfungi Associated with the Fungus-Growing Ant Symbiosis
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