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Phylogenetic Codivergence Supports Coevolution of Mimetic Heliconius Butterflies
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1 of the 66 references listed on this page is in the Retraction Watch database as retracted (export 2026-10-28): 10.1186/1471-2148-4-18 (notice 2015-11-05).
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1007/978-94-009-6533-1openalex-snapshot
Atlas of Neotropical Lepidoptera
inferredcites →https://doi.org/10.1016/0040-5809(75)90020-9openalex-snapshot
On the number of segregating sites in genetical models without recombination
inferredcites →https://doi.org/10.1016/j.ympev.2008.09.008openalex-snapshot
Does gene flow destroy phylogenetic signal? The performance of three methods for estimating species phylogenies in the presence of gene flow
inferredcites →https://doi.org/10.1016/s0025-5564(97)10012-8openalex-snapshot
Jungles: a new solution to the host/parasite phylogeny reconciliation problem
inferredcites →https://doi.org/10.1016/s0169-5347(98)01483-9openalex-snapshot
Diversity in mimicry: paradox or paradigm?
inferredcites →https://doi.org/10.1016/s0960-9822(02)00631-0openalex-snapshot
Evolution: Mimicry meets the mitochondrion
inferredcites →https://doi.org/10.1023/a:1011060330515openalex-snapshot
Causes and Consequences of a Lack of Coevolution in Müllerian mimicry
inferredcites →https://doi.org/10.1038/35018159openalex-snapshot
Preventing cyanide release from leaves
inferredcites →https://doi.org/10.1038/35053066openalex-snapshot
Three-butterfly system provides a field test of müllerian mimicry
inferredcites →https://doi.org/10.1038/nrg2526openalex-snapshot
Effective population size and patterns of molecular evolution and variation
inferredcites →https://doi.org/10.1038/nrg795openalex-snapshot
Genealogical trees, coalescent theory and the analysis of genetic polymorphisms
inferredcites →https://doi.org/10.1046/j.1420-9101.1988.1010089.xopenalex-snapshot
Futuyma, D. J. 1986. Evolutionary Biology 2nd edition, Sinauer Associates Inc. Sunderland, Mass.
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.1523-1739.1996.10061500.xopenalex-snapshot
Relationship of Genetic Variation to Population Size in Wildlife
inferredcites →https://doi.org/10.1073/pnas.0306243101openalex-snapshot
Historical demography of Müllerian mimicry in the neotropical Heliconius butterflies
inferredcites →https://doi.org/10.1073/pnas.0509685103openalex-snapshot
Linkage of butterfly mate preference and wing color preference cue at the genomic location of wingless
inferredcites →https://doi.org/10.1073/pnas.0911572107openalex-snapshot
Dissecting comimetic radiations in Heliconius reveals divergent histories of convergent butterflies
inferredcites →https://doi.org/10.1073/pnas.0913022107openalex-snapshot
Bayesian species delimitation using multilocus sequence data
inferredcites →https://doi.org/10.1073/pnas.1110096108openalex-snapshot
Wing patterning gene redefines the mimetic history of Heliconius butterflies
inferredcites →https://doi.org/10.1073/pnas.91.14.6491openalex-snapshot
Rapid morphological radiation and convergence among races of the butterfly Heliconius erato inferred from patterns of mitochondrial DNA evolution.
inferredcites →https://doi.org/10.1080/01621459.1927.10502953openalex-snapshot
Probable Inference, the Law of Succession, and Statistical Inference
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/10.1080/10635150500354928openalex-snapshot
Inferring Phylogeny Despite Incomplete Lineage Sorting
inferredcites →https://doi.org/10.1093/genetics/145.3.833openalex-snapshot
A Coalescent Estimator of the Population Recombination Rate
inferredcites →https://doi.org/10.1093/genetics/145.3.847openalex-snapshot
Estimating Ancestral Population Parameters
inferredcites →https://doi.org/10.1093/genetics/16.2.97openalex-snapshot
EVOLUTION IN MENDELIAN POPULATIONS
inferredcites →https://doi.org/10.1093/molbev/msn083openalex-snapshot
jModelTest: Phylogenetic Model Averaging
inferredcites →https://doi.org/10.1093/molbev/msp274openalex-snapshot
Bayesian Inference of Species Trees from Multilocus Data
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.a004042openalex-snapshot
Phylogenetic Discordance at the Species Boundary: Comparative Gene Genealogies Among Rapidly Radiating Heliconius Butterflies
inferredcites →https://doi.org/10.1093/oxfordjournals.molbev.a026201openalex-snapshot
Multiple Comparisons of Log-Likelihoods with Applications to Phylogenetic Inference
inferredcites →https://doi.org/10.1093/sysbio/syr071openalex-snapshot
Evaluation of a Bayesian Coalescent Method of Species Delimitation
inferredcites →https://doi.org/10.1098/rspb.1974.0082openalex-snapshot
Quaternary refugia in tropical America: evidence from race formation in Heliconius butterflies
inferredcites →https://doi.org/10.1098/rspb.2007.1378openalex-snapshot
The population genetics of mimetic diversity in Heliconius butterflies
inferredcites →https://doi.org/10.1098/rspb.2011.1430openalex-snapshot
Cretaceous origin and repeated tertiary diversification of the redefined butterflies
inferredcites →https://doi.org/10.1098/rstb.1985.0066openalex-snapshot
Genetics and the evolution of muellerian mimicry in heliconius butterflies
inferredcites →https://doi.org/10.1109/tac.1974.1100705openalex-snapshot
A new look at the statistical model identification
inferredcites →https://doi.org/10.1111/j.1095-8312.1986.tb01772.xopenalex-snapshot
Field observations and feeding experiments on the responses of rufous-tailed jacamars (Galbula ruficauda) to free-flying butterflies in a tropical rainforest
inferredcites →https://doi.org/10.1111/j.1095-8312.2007.00830.xopenalex-snapshot
Do pollen feeding, pupal-mating and larval gregariousness have a single origin in Heliconius butterflies? Inferences from multilocus DNA sequence data
inferredcites →https://doi.org/10.1111/j.1096-0031.2010.00326.xopenalex-snapshot
Phylogenetics and divergence times of Papilioninae (Lepidoptera) with special reference to the enigmatic genera Teinopalpus and Meandrusa
inferredcites →https://doi.org/10.1111/j.1096-3642.1860.tb00146.xopenalex-snapshot
XXXII. Contributions to an Insect Fauna of the Amazon Valley. Lepidoptera: Heliconidae.
inferredcites →https://doi.org/10.1111/j.1365-2311.1916.tb03123.xopenalex-snapshot
IV. On Specific and Mimetic Relationships in the genus Heliconius, L.
inferredcites →https://doi.org/10.1111/j.1365-2311.1987.tb00987.xopenalex-snapshot
The evolutionary dynamics of batesian and muellerian mimicry: similarities and differences
inferredcites →https://doi.org/10.1111/j.1365-294x.2008.03934.xopenalex-snapshot
A hybrid zone provides evidence for incipient ecological speciation in Heliconius butterflies
inferredcites →https://doi.org/10.1111/j.1420-9101.2006.01199.xopenalex-snapshot
Dynamics of the evolution of Batesian mimicry: molecular phylogenetic analysis of ant‐mimicking Myrmarachne (Araneae: Salticidae) species and their ant models
inferredcites →https://doi.org/10.1111/j.1558-5646.1980.tb04849.xopenalex-snapshot
WHEN IS IT COEVOLUTION?
inferredcites →https://doi.org/10.1111/j.1558-5646.1996.tb04486.xopenalex-snapshot
PARALLEL RACE FORMATION AND THE EVOLUTION OF MIMICRY INHELICONIUSBUTTERFLIES: A PHYLOGENETIC HYPOTHESIS FROM MITOCHONDRIAL DNA SEQUENCES
inferredcites →https://doi.org/10.1111/j.1558-5646.2010.01097.xopenalex-snapshot
CALIBRATING DIVERGENCE TIMES ON SPECIES TREES VERSUS GENE TREES: IMPLICATIONS FOR SPECIATION HISTORY OF APHELOCOMA JAYS
inferredcites →https://doi.org/10.1111/j.1744-7429.2003.tb00589.xopenalex-snapshot
Does Müllerian Mimicry Work in Nature? Experiments with Butterflies and Birds (Tyrannidae)1
inferredcites →https://doi.org/10.1126/science.1179141openalex-snapshot
Polymorphic Butterfly Reveals the Missing Link in Ecological Speciation
inferredcites →https://doi.org/10.1126/science.1208227openalex-snapshot
optix Drives the Repeated Convergent Evolution of Butterfly Wing Pattern Mimicry
inferredcites →https://doi.org/10.1126/science.176.4037.936openalex-snapshot
Natural Selection for Müllerian Mimicry in Heliconius erato in Costa Rica
inferredcites →https://doi.org/10.1146/annurev.en.26.010181.002235openalex-snapshot
The Biology of Heliconius and Related Genera
inferredcites →https://doi.org/10.1163/9789004630567openalex-snapshot
Atlas of neotropical Lepidoptera
inferredcites →https://doi.org/10.1186/1471-2148-4-18openalex-snapshot
RETRACTED ARTICLE: TREEFINDER: a powerful graphical analysis environment for molecular phylogenetics
inferredcites →https://doi.org/10.1186/1471-2148-7-214openalex-snapshot
BEAST: Bayesian evolutionary analysis by sampling trees
inferredcites →https://doi.org/10.1186/1741-7007-4-11openalex-snapshot
Polyphyly and gene flow between non-sibling Heliconius species
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.pgen.1000794openalex-snapshot
Genomic Hotspots for Adaptation: The Population Genetics of Müllerian Mimicry in the Heliconius melpomene Clade
inferredcites →https://doi.org/10.1371/journal.pgen.1000796openalex-snapshot
Genomic Hotspots for Adaptation: The Population Genetics of Müllerian Mimicry in Heliconius erato
inferredcites →https://doi.org/10.1371/journal.pgen.1001016openalex-snapshot
Evaluation of Candidate Stromal Epithelial Cross-Talk Genes Identifies Association between Risk of Serous Ovarian Cancer and TERT, a Cancer Susceptibility “Hot-Spot”
inferredcites →https://doi.org/10.2307/2410794openalex-snapshot
Parallel Race Formation and the Evolution of Mimicry in Heliconius Butterflies: A Phylogenetic Hypothesis from Mitochondrial DNA Sequences
inferredcites →https://doi.org/10.7208/chicago/9780226797670.001.0001openalex-snapshot
The Coevolutionary Process
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1080/00222933.2019.1669730zenodo-depositor-declared
A remarkable example of suspected Batesian mimicry of Gaboon Vipers (Reptilia: Viperidae:Bitis gabonica) by Congolese Giant Toads (Amphibia: Bufonidae:Sclerophrys channingi)
inferred← citeshttps://doi.org/10.1007/978-3-319-24235-4_3openalex-snapshot
Updating Genomic Data of Lepidoptera
inferred← citeshttps://doi.org/10.1007/978-3-662-43550-2_20openalex-snapshot
Event-Based Cophylogenetic Comparative Analysis
inferred← citeshttps://doi.org/10.1007/s40279-016-0484-2openalex-snapshot
Monitoring Athletic Training Status Through Autonomic Heart Rate Regulation: A Systematic Review and Meta-Analysis
inferred← citeshttps://doi.org/10.1016/b978-0-12-801213-0.00012-5openalex-snapshot
Reconstructing the Phylogeny
inferred← citeshttps://doi.org/10.1016/j.cois.2016.09.006openalex-snapshot
Advances using molecular data in insect systematics
inferred← citeshttps://doi.org/10.1016/j.cois.2016.10.004openalex-snapshot
Testing cospeciation through large-scale cophylogenetic studies
inferred← citeshttps://doi.org/10.1016/j.compbiolchem.2015.02.003openalex-snapshot
A time and space complexity reduction for coevolutionary analysis of trees generated under both a Yule and Uniform model
inferred← citeshttps://doi.org/10.1016/j.jmb.2022.167563openalex-snapshot
Host diversification is concurrent with linear motif evolution in a Mastadenovirus hub protein
inferred← citeshttps://doi.org/10.1017/cbo9781139794749.028openalex-snapshot
When is co-phylogeny evidence ofcoevolution?
inferred← citeshttps://doi.org/10.1038/s41598-020-69771-9openalex-snapshot
Clathrin mediated endocytosis is involved in the uptake of exogenous double-stranded RNA in the white mold phytopathogen Sclerotinia sclerotiorum
inferred← citeshttps://doi.org/10.1073/pnas.1907068116openalex-snapshot
Parallel evolution of ancient, pleiotropic enhancers underlies butterfly wing pattern mimicry
inferred← citeshttps://doi.org/10.1080/23256214.2014.906070openalex-snapshot
An improved node mapping algorithm for the cophylogeny reconstruction problem
inferred← citeshttps://doi.org/10.1089/cmb.2015.0111openalex-snapshot
RASCAL: A Randomized Approach for Coevolutionary Analysis
inferred← citeshttps://doi.org/10.1093/cz/zow018openalex-snapshot
Phylogenetic framework for coevolutionary studies: a compass for exploring jungles of tangled trees
inferred← citeshttps://doi.org/10.1093/gbe/evz202openalex-snapshot
Comparative Transcriptomics Provides Insights into Reticulate and Adaptive Evolution of a Butterfly Radiation
inferred← citeshttps://doi.org/10.1093/molbev/msy209openalex-snapshot
Genome-Wide Regulatory Adaptation Shapes Population-Level Genomic Landscapes in Heliconius
inferred← citeshttps://doi.org/10.1093/sysbio/syaa033openalex-snapshot
Random Tanglegram Partitions (Random TaPas): An Alexandrian Approach to the Cophylogenetic Gordian Knot
inferred← citeshttps://doi.org/10.1093/sysbio/syv007openalex-snapshot
Multilocus Species Trees Show the Recent Adaptive Radiation of the Mimetic Heliconius Butterflies
inferred← citeshttps://doi.org/10.1093/zoolinnean/zlaf160openalex-snapshot
Coalescent species’ delimitation in mimetic beetles of the genus Ceroglossus Solier (Coleoptera: Carabidae): the importance of species’ delineation to the understanding of the drivers of phenotypic diversity
inferred← citeshttps://doi.org/10.1098/rspb.2012.2302openalex-snapshot
Introgression of wing pattern alleles and speciation via homoploid hybridization inHeliconiusbutterflies: a review of evidence from the genome
inferred← citeshttps://doi.org/10.1098/rspb.2016.0585openalex-snapshot
Australian spiny mountain crayfish and their temnocephalan ectosymbionts: an ancient association on the edge of coextinction?
inferred← citeshttps://doi.org/10.1101/2025.05.15.653894openalex-snapshot
Macroevolutionary Rates of Species Interactions: Approximate Bayesian Inference from Cophylogenies
inferred← citeshttps://doi.org/10.1101/gr.169292.113openalex-snapshot
Population genomics of parallel hybrid zones in the mimetic butterflies, H. melpomene and H. erato
inferred← citeshttps://doi.org/10.1111/ele.14059openalex-snapshot
Explosive networking: The role of adaptive host radiations and ecological opportunity in a species‐rich host–parasite assembly
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.12812openalex-snapshot
Wing patterning genes and coevolution of Müllerian mimicry inHeliconiusbutterflies: Support from phylogeography, cophylogeny, and divergence times
inferred← citeshttps://doi.org/10.1111/jeb.12672openalex-snapshot
The diversification of Heliconius butterflies: what have we learned in 150 years?
inferred← citeshttps://doi.org/10.1111/jeb.14221openalex-snapshot
Assessing co-diversification in host-associated microbiomes
inferred← citeshttps://doi.org/10.1111/mec.12844openalex-snapshot
Phylogeography of Heliconius cydno and its closest relatives: disentangling their origin and diversification
inferred← citeshttps://doi.org/10.1111/nph.16176openalex-snapshot
The nature of interspecific interactions and co‐diversification patterns, as illustrated by the fig microcosm
inferred← citeshttps://doi.org/10.1126/sciadv.aaw4967openalex-snapshot
Deep learning on butterfly phenotypes tests evolution’s oldest mathematical model
inferred← citeshttps://doi.org/10.1186/1471-2105-15-s16-s14openalex-snapshot
Introducing TreeCollapse: a novel greedy algorithm to solve the cophylogeny reconstruction problem
inferred← citeshttps://doi.org/10.1186/s13015-016-0077-5openalex-snapshot
Towards sub-quadratic time and space complexity solutions for the dated tree reconciliation problem
inferred← citeshttps://doi.org/10.1371/journal.pbio.3000597openalex-snapshot
Selective sweeps on novel and introgressed variation shape mimicry loci in a butterfly adaptive radiation
inferred← citeshttps://doi.org/10.1371/journal.pone.0057033openalex-snapshot
Multi-Allelic Major Effect Genes Interact with Minor Effect QTLs to Control Adaptive Color Pattern Variation in Heliconius erato
inferred← citeshttps://doi.org/10.1371/journal.pone.0112942openalex-snapshot
Müllerian Mimicry as a Result of Codivergence between Velvet Ants and Spider Wasps
inferred← citeshttps://doi.org/10.1534/genetics.114.172387openalex-snapshot
The Functional Basis of Wing Patterning in Heliconius Butterflies: The Molecules Behind Mimicry
inferred← citeshttps://doi.org/10.22541/au.163274253.31016446/v1openalex-snapshot
The role of phylogeny and ecological opportunity in host-parasite interactions: network metrics, host repertoire, and network link prediction.
inferred← citeshttps://doi.org/10.22541/au.164328685.58498923/v1openalex-snapshot
The role of phylogeny, ecological opportunity, and adaptive radiation in host-parasite interactions: network metrics, host repertoire, and network link prediction
inferred← citeshttps://doi.org/10.26076/900a-5a50openalex-snapshot
Molecular Systematics, Historical Biogeography, and Evolution of Spider Wasps (Hymenoptera: Pompilidae)
inferred← citeshttps://doi.org/10.7287/peerj.573v0.1/reviews/1openalex-snapshot
Peer Review #1 of "Phylogenetic congruence of lichenised fungi and algae is affected by spatial scale and taxonomic diversity (v0.1)"
inferred← citeshttps://doi.org/10.7287/peerj.573v0.1/reviews/2openalex-snapshot
Peer Review #2 of "Phylogenetic congruence of lichenised fungi and algae is affected by spatial scale and taxonomic diversity (v0.1)"
inferred← citeshttps://doi.org/10.7717/peerj.573openalex-snapshot
Phylogenetic congruence of lichenised fungi and algae is affected by spatial scale and taxonomic diversity
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