References
- Ahmed, M. Z., Araujo-Jnr, E. V., Welch, J. J., & Kawahara, A. Y. (2015). Wolbachia in butterflies and moths: Geographic structure in infection frequency. Frontiers in Zoology, 12, 16. https://doi.org/https://doi.org/10.1186/s12983-015-0107-z
- Aubier, T. G., Kokko, H., & Joron, M. (2019). Coevolution of male and female mate choice can destabilize reproductive isolation. Nature Communication, 10, 5122.
- Baldo, L., Dunning Hotopp, J. C., Jolley, K. A., Bordenstein, S. R., Biber, S. A., Choudhury, R. R., Hayashi, C., Maiden, M. C., Tettelin, H., & Werren, J. H. (2006). Multilocus sequence typing system for the endosymbiont Wolbachia pipientis. Applied and Environmental Microbiology, 72, 7098–7110. https://doi.org/https://doi.org/10.1128/AEM.00731-06
- Brower, A. V. Z. (1994). Rapid morphological radiation and convergence among races of the butterfly Heliconius erato inferred from patterns of mitochondrial DNA evolution. Proceedings of the National Academy of Sciences of the United States of America, 91, 6491–6495. https://doi.org/https://doi.org/10.1073/pnas.91.14.6491
- Caterino, M. S., & Sperling, F. A. (1999). Papilio phylogeny based on mitochondrial cytochrome oxidase I and II genes. Molecular Phylogenetics and Evolution, 11, 122–137. https://doi.org/https://doi.org/10.1006/mpev.1998.0549
- Clement, M., Posada, D., & Crandall, K. A. (2000). TCS: A computer program to estimate gene genealogies. Molecular Ecology, 9, 1657–1659. https://doi.org/https://doi.org/10.1046/j.1365-294x.2000.01020.x
- Cooper, B. S., Ginsberg, P. S., Turelli, M., & Matute, D. R. (2017). Wolbachia in the Drosophila yakuba complex: Pervasive frequency variation and weak cytoplasmic incompatibility, but no apparent effect on reproductive isolation. Genetics, 205, 333–351. https://doi.org/https://doi.org/10.1534/genetics.116.196238
- Crane, J. (1955). Imaginal behavior of a Trinidad butterfly, Heliconius erato hydara Hewitson, with special reference to the social use of color. Zoologica; Scientific Contributions of the New York Zoological Society, 40, 167–196.
- Descimon, H., & Mallet, J. (2009). Bad species - how ecology and evolution confuse butterfly taxonomy. In J. Settele, T. Shreeve, M. Konvicka, & H. Van Dyck (Eds.), Ecology of butterflies in Europe (pp. 219–249). Cambridge University Press.
- Dincă, V., Lee, K. M., Vila, R., & Mutanen, M. (2019 The conundrum of species delimitation: A genomic perspective on a mitogenetically super-variable butterfly. Proceedings of the Royal Society B: Biological Sciences, 286, 20191311.
- Duplouy, A., & Hornett, E. A. (2018). Uncovering the hidden players in Lepidoptera biology: The heritable microbial endosymbionts. PeerJ, 6, e4629 https://doi.org/https://doi.org/10.7717/peerj.4629
- Duplouy, A., Pranter, R., Warren-Gash, H., Tropek, R., & Wahlberg, N. (2020). Towards unravelling Wolbachia global exchange: a contribution from the Bicyclus and Mylothris butterflies in the Afrotropics. BioMedCentral Microbiology, 20. https://doi.org/https://doi.org/10.1186/s12866-020-02011-2
- Emelianov, I., Marec, F., & Mallet, J. (2004 Genomic evidence for divergence with gene flow in host races of the larch budmoth. Proceedings of the Royal Society B – Biological Sciences, 271, 97–105.
- Excoffier, L., & Lischer, H. E. L. (2010). Arlequin suite ver 3.5: A new series of programs to perform population genetics analyses under Linux and Windows. Molecular Ecology Resources, 10, 564–567. https://doi.org/https://doi.org/10.1111/j.1755-0998.2010.02847.x
- Excoffier, L., Smouse, P. E., & Quattro, J. M. (1992). Analysis of molecular variance inferred from metric distances among DNA haplotypes: Application to human mitochondrial DNA restriction data. Genetics, 131, 479–491.
- Francini, R. B. (1989). Biologia e ecologia das borboletas Actinote (Lepidoptera: Nymphalidae, Acraeinae) na transição subtropical do sudeste do Brasil. Ms Thesis. Universidade Estadual de Campinas, Campinas. 236 p.
- Fujii, Y., Kageyama, D., Hoshizaki, S., Ishikawa, H., & Sasaki, T. (2001). Transfection of Wolbachia in Lepidoptera: The feminizer of the adzuki bean borer Ostrinia scapulalis causes male killing in the Mediterranean flour moth Ephestia kuehniella. Proceedings of the Royal Society of London. Series B: Biological Sciences, 268, 855–859.
- Hebert, P. D. N., Cywinska, A., Ball, S. L., & Dewaard, J. R. (2003a). Biological identifications through DNA barcodes. Proceedings of the Royal Society of London Series B - Biological Sciences, 270, 313–321. https://doi.org/https://doi.org/10.1098/rspb.2002.2218
- Hebert, P. D. N., Ratnasingham, S., & Dewaard, J. R. (2003b). Barcoding animal life: Cytochrome c oxidase subunit 1 divergences among closely related species. Proceedings of the Royal Society of London Series B - Biological Sciences, 270, S96–S99.
- Hoang, D. T., Chernomor, O., Von Haeseler, A., Minh, B. Q., & Vinh, L. S. (2018). UFBoot2: Improving the ultrafast bootstrap approximation. Molecular Biology and Evolution, 35, 518–522. https://doi.org/https://doi.org/10.1093/molbev/msx281
- Hurst, G. D., & Jiggins, F. M. (2005). Problems with mitochondrial DNA as a marker in population, phylogeographic and phylogenetic studies: The effects of inherited symbionts. Proceedings of the Royal Society of London Series B - Biological Sciences, 272, 1525–1534.
- Ilinsky, Y., & Kosterin, O. E. (2017). Molecular diversity of Wolbachia in Lepidoptera: Prevalent allelic content and high recombination of MLST genes. Molecular Phylogenetics and Evolution, 109, 164–179. https://doi.org/https://doi.org/10.1016/j.ympev.2016.12.034
- Jaenike, J., Dyer, K. A., Cornish, C., & Minhas, M. S. (2006). Asymmetrical reinforcement and Wolbachia infection in Drosophila. Public Library of Science Biology, 4, e325. https://doi.org/https://doi.org/10.1371/journal.pbio.0040325
- Jiggins, C. D., Naisbit, R. E., Coe, R. L., & Mallet, J. (2001a). Reproductive isolation caused by colour pattern mimicry. Nature, 411, 302–305. https://doi.org/https://doi.org/10.1038/35077075
- Jiggins, F. M. (2003). Male-killing Wolbachia and mitochondrial DNA: Selective sweeps, hybrid introgression and parasite population dynamics. Genetics, 164, 5–12. https://doi.org/https://doi.org/10.1093/genetics/164.1.5
- Jiggins, F. M., Bentley, J. K., Majerus, M. E. N., & Hurst, G. D. D. (2001b). How many species are infected with Wolbachia? Cryptic sex ratio distorters revealed to be common by intensive sampling. Proceedings of the Royal Society of London, Series B: Biological Sciences, 268, 1123–1126. https://doi.org/https://doi.org/10.1098/rspb.2001.1632
- Jiggins, F. M., Bentley, J. K., Majerus, M. E. N., & Hurst, G. D. D. (2002). Recent changes in phenotype and patterns of host specialization in Wolbachia bacteria. Molecular Ecology, 11, 1275–1283. https://doi.org/https://doi.org/10.1046/j.1365-294x.2002.01532.x
- Jiggins, F. M., Hurst, G. D. D., & Majerus, M. E. N. (1998). Sex ratio distortion in Acraea encedon (Lepidoptera: Nymphalidae) is caused by a male-killing bacterium. Heredity, 81, 87–91. https://doi.org/https://doi.org/10.1046/j.1365-2540.1998.00357.x
- Jiggins, F. M., Hurst, G. D. D., Dolman, C. E., & Majerus, M. E. N. (2000). High-prevalence male-killing Wolbachia in the butterfly Acraea encedana. Journal of Evolutionary Biology, 13, 495–501.
- Jiggins, F. M., Hurst, G. D., Schulenburg, J. H., & Majerus, M. E. (2001c). Two male-killing Wolbachia strains coexist within a population of the butterfly Acraea encedon. Heredity, 86, 161–166. https://doi.org/https://doi.org/10.1046/j.1365-2540.2001.00804.x
- Jiggins, F. M., Von Der Schulenburg, J. H., Hurst, G. D., & Majerus, M. E. (2001d). Recombination confounds interpretations of Wolbachia evolution. Proceedings. Biological Sciences, 268, 1423–1427. https://doi.org/https://doi.org/10.1098/rspb.2001.1656
- Jukes, T. H., & Cantor, C. R. (1969). Chapter 24 - Evolution of protein molecules. In H. N. Munro (Ed.), Mammalian protein metabolism (pp. 21–132). Academic Press.
- Kageyama, D., Nishimura, G., Hoshizaki, S., & Ishikawa, Y. (2002). Feminizing Wolbachia in an insect, Ostrinia furnacalis (Lepidoptera: Crambidae). Heredity, 88, 444–449. https://doi.org/https://doi.org/10.1038/sj.hdy.6800077
- Kalyaanamoorthy, S., Minh, B. Q., Wong, T. K. F., Von Haeseler, A., & Jermiin, L. S. (2017). ModelFinder: Fast model selection for accurate phylogenetic estimates. Nature Methods, 14, 587–589. https://doi.org/https://doi.org/10.1038/nmeth.4285
- Kearse, M., Moir, R., Wilson, A., Stones-Havas, S., Cheung, M., Sturrock, S., Buxton, S., Cooper, A., Markowitz, S., Duran, C., Thierer, T., Ashton, B., Meintjes, P., & Drummond, A. (2012). Geneious Basic: An integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics (Oxford, England), 28, 1647–1649. https://doi.org/https://doi.org/10.1093/bioinformatics/bts199
- Kodandaramaiah, U., Weingartner, E., Janz, N., Dalén, L., & Nylin, S. (2011). Population structure in relation to host-plant ecology and Wolbachia infestation in the comma butterfly. Journal of Evolutionary Biology, 24, 2173–2185. https://doi.org/https://doi.org/10.1111/j.1420-9101.2011.02352.x
- Kronforst, M. R., & Papa, R. (2015). The functional basis of wing patterning in Heliconius butterflies: The molecules behind mimicry. Genetics, 200, 1–19. https://doi.org/https://doi.org/10.1534/genetics.114.172387
- Lamas, G. (2004). Checklist: Part 4A. Hesperioidea-Papilionoidea. In J. B. Heppner (Ed.), Atlas of Neotropical Lepidoptera (p. xxxvi + 439). Association for Tropical Lepidoptera/Scientific Publishers.
- Lamas, G. (2008). La sistemática sobre mariposas (Lepidoptera: Hesperioidea y Papilionoidea) en el mundo: Estado actual y perspectivas futuras. In J. Llorente-Bousquets & A. Lanteri (Eds.), Contribuciones taxonómicas en órdenes de insectos hiperdiversos (pp. 57–70). Las Prensas de Ciencias, UNAM.
- Leigh, J. W., & Bryant, D. (2015). PopART: Full-feature software for haplotype network construction. Methods in Ecology and Evolution, 6, 1110–1116. https://doi.org/https://doi.org/10.1111/2041-210X.12410
- Martin, A., Mcculloch, K. J., Patel, N. H., Briscoe, A. D., Gilbert, L. E., & Reed, R. D. (2014). Multiple recent co-options of Optix associated with novel traits in adaptive butterfly wing radiations. EvoDevo, 5, 7. https://doi.org/https://doi.org/10.1186/2041-9139-5-7
- Merrill, R. M., Rastas, P., Martin, S. H., Melo, M. C., Barker, S., Davey, J., Mcmillan, W. O., & Jiggins, C. D. (2019). Genetic dissection of assortative mating behavior. Public Library of Science Biology, 17, e2005902. https://doi.org/https://doi.org/10.1371/journal.pbio.2005902
- Miller, W. J., Ehrman, L., & Schneider, D. (2010). Infectious speciation revisited: Impact of symbiont-depletion on female fitness and mating behavior of Drosophila paulistorum. Public Library of Science Pathogens, 6, e1001214. https://doi.org/https://doi.org/10.1371/journal.ppat.1001214
- Nadeau, N. J., Pardo-Diaz, C., Whibley, A., Supple, M. A., Saenko, S. V., Wallbank, R. W. R., Wu, G. C., Maroja, L., Ferguson, L., Hanly, J. J., Hines, H., Salazar, C., Merrill, R. M., Dowling, A. J., Ffrench-Constant, R. H., Llaurens, V., Joron, M., Mcmillan, W. O., & Jiggins, C. D. (2016). The gene cortex controls mimicry and crypsis in butterflies and moths. Nature, 534, 106–123. https://doi.org/https://doi.org/10.1038/nature17961
- Neild, A. F. E. (2008). The Butterflies of Venezuela, Part 2: Nymphalidae II (Acraeinae, Libytheinae, Nymphalinae, Ithomiinae, Morphinae). Meridian Publications.
- O’Neill, S. L., Giordano, R., Colbert, A. M., Karr, T. L., & Robertson, H. M. (1992). 16S rRNA phylogenetic analysis of the bacterial endosymbionts associated with cytoplasmic incompatibility in insects. Proceedings of the National Academy of Sciences of the United States of America, 89, 2699–2702.
- Paluch, M. (2006). Revisão das espécies de Actinote Hübner, [1819] (Lepidoptera, Nymphalidae, Heliconiinae, Acraeini) (p. xix + 410). Universidade Federal do Paraná, City.
- Paluch, M., Casagrande, M., & Mielke, O. (2006). Three species and two new subspecies of Actinote Hübner (Nymphalidae, Heliconiinae, Acraeini). Revista Brasileira de Zoologia, 23, 764–778. https://doi.org/https://doi.org/10.1590/S0101-81752006000300022
- Puillandre, N., Lambert, A., Brouillet, S., & Achaz, G. (2012). ABGD, Automatic Barcode Gap Discovery for primary species delimitation. Molecular Ecology, 21, 1864–1877. https://doi.org/https://doi.org/10.1111/j.1365-294X.2011.05239.x
- Reed, R. D., Papa, R., Martin, A., Hines, H. M., Counterman, B. A., Pardo-Diaz, C., Jiggins, C. D., Chamberlain, N. L., Kronforst, M. R., Chen, R., Halder, G., Nijhout, H. F., & Mcmillan, W. O. (2011). optix drives the repeated convergent evolution of butterfly wing pattern mimicry. Science (New York, N.Y.), 333, 1137–1141. https://doi.org/https://doi.org/10.1126/science.1208227
- Ritter, S., Michalski, S. G., Settele, J., Wiemers, M., Fric, Z. F., Sielezniew, M., Šašić, M., Rozier, Y., & Durka, W. (2013). Wolbachia infections mimic cryptic speciation in two parasitic butterfly species, Phengaris teleius and P. nausithous (Lepidoptera: Lycaenidae). Public Library of Science One, 8, e78107. https://doi.org/https://doi.org/10.1371/journal.pone.0078107
- Rousset, F., & Solignac, M. (1995). Evolution of single and double Wolbachia symbioses during speciation in the Drosophila simulans complex. Proceedings of the National Academy of Sciences of the United States of America, 92, 6389–6393.
- Rousset, F., Vautrin, D., & Solignac, M. (1992). Molecular identification of Wolbachia, the agent of cytoplasmic incompatibility in Drosophila simulans, and variability in relation with host mitochondrial types. Proceedings of the Royal Society of London, Series B: Biological Sciences, 247, 163–168.
- Russell, J. A., Goldman-Huertas, B., Moreau, C. S., Baldo, L., Stahlhut, J. K., Werren, J. H., & Pierce, N. E. (2009). Specialization and geographic isolation among Wolbachia symbionts from ants and lycaenid butterflies. Evolution; International Journal of Organic Evolution, 63, 624–640. https://doi.org/https://doi.org/10.1111/j.1558-5646.2008.00579.x
- Shoemaker, D. D., Katju, V., & Jaenike, J. (1999). Wolbachia and the evolution of reproductive isolation between Drosophila recens and DROSOPHILA SUBQUINARIA. Evolution; International Journal of Organic Evolution, 53, 1157–1164. https://doi.org/https://doi.org/10.1111/j.1558-5646.1999.tb04529.x
- Silva-Brandão, K. L., Freitas, A. V. L., Brower, A. V. Z., & Solferini, V. N. (2005). Phylogenetic relationships of the New World Troidini swallowtails (Lepidoptera: Papilionidae) based on COI, COII, and EF-1 alpha genes. Molecular Phylogenetics and Evolution, 36, 468–483. https://doi.org/https://doi.org/10.1016/j.ympev.2005.04.007
- Silva-Brandão, K. L., Lyra, M. L., & Freitas, A. V. L. (2009). Barcoding Lepidoptera: Current situation and perspectives on the usefulness of a contentious technique. Neotropical Entomology, 38, 441–451. https://doi.org/https://doi.org/10.1590/s1519-566x2009000400001
- Silva-Brandão, K. L., Wahlberg, N., Francini, R. B., Azeredo-Espin, A. M. L., Brown, K. S., Paluch, M., Lees, D. C., & Freitas, A. V. L. (2008). Phylogenetic relationships of butterflies of the tribe Acraeini (Lepidoptera, Nymphalidae, Heliconiinae) and the evolution of host plant use. Molecular Phylogenetics and Evolution, 46, 515–531. https://doi.org/https://doi.org/10.1016/j.ympev.2007.11.024
- Slatkin, M. (1995). A measure of population subdivision based on microsatellite allele frequencies. Genetics, 139, 457–462. https://doi.org/https://doi.org/10.1093/genetics/139.1.457
- Stecher, G., Tamura, K., & Kumar, S. (2020). Molecular Evolutionary Genetics Analysis (MEGA) for macOS. Molecular Biology and Evolution, 37, 1237–1239. https://doi.org/https://doi.org/10.1093/molbev/msz312
- Sucháčková Bartoňová, A., Konvička, M., Marešová, J., Wiemers, M., Ignatev, N., Wahlberg, N., Schmitt, T. F., & Fric, Z. (2021). Wolbachia affects mitochondrial population structure in two systems of closely related Palaearctic blue butterflies. Scientific Reports, 11, 3019. https://doi.org/https://doi.org/10.1038/s41598-021-82433-8
- Tamura, K. (1992). Estimation of the number of nucleotide substitutions when there are strong transition-transversion and G + C-content biases. Molecular Biology and Evolution, 9, 678–687.
- Templeton, A. R., Crandall, K. A., & Sing, C. F. (1992). A cladistic analysis of phenotypic associations with haplotypes inferred from restriction endonuclease mapping and DNA sequence data. III. Cladogram estimation. Genetics, 132, 619–633.
- Trifinopoulos, J., Nguyen, L. T., Von Haeseler, A., & Minh, B. Q. (2016). W-IQ-TREE: A fast online phylogenetic tool for maximum likelihood analysis. Nucleic Acids Research, 44, W232–235. https://doi.org/https://doi.org/10.1093/nar/gkw256
- Turelli, M. (1994). Evolution of incompatibility-inducing microbes and their hosts. Evolution; International Journal of Organic Evolution, 48, 1500–1513. https://doi.org/https://doi.org/10.1111/j.1558-5646.1994.tb02192.x
- Van Belleghem, S. M., Rastas, P., Papanicolaou, A., Martin, S. H., Arias, C. F., Supple, M. A., Hanly, J. J., Mallet, J., Lewis, J. J., Hines, H. M., Ruiz, M., Salazar, C., Linares, M., Moreira, G. R. P., Jiggins, C. D., Counterman, B. A., Mcmillan, W. O., & Papa, R. (2017). Complex modular architecture around a simple toolkit of wing pattern genes. Nature Ecology and Evolution, 1, 0052.
- Via, S. (2012). Divergence hitchhiking and the spread of genomic isolation during ecological speciation-with-gene-flow. Philosophical Transactions of the Royal Society of London, Series B, Biological Sciences, 367, 451–460. https://doi.org/https://doi.org/10.1098/rstb.2011.0260
- Werren, J. H. (1997). Biology of Wolbachia. Annual Review of Entomology, 42, 587–609. https://doi.org/https://doi.org/10.1146/annurev.ento.42.1.587
- Werren, J. H. (1998). Wolbachia and speciation. In D. J. Howard & S. H. Berlocher (Eds.), Endless forms – species and speciation (pp. 245–260). Oxford University Press.
- Werren, J. H., Baldo, L., & Clark, M. E. (2008). Wolbachia: Master manipulators of invertebrate biology. Nature Reviews. Microbiology, 6, 741–751. https://doi.org/https://doi.org/10.1038/nrmicro1969
- Werren, J. H., Windsor, D., & Guo, L. R. (1995). Distribution of Wolbachia among neotropical arthropods. Proceedings of the Royal Society of London, Series B: Biological Sciences, 262, 197–204.
- Zhou, W., Rousset, F., & O’Neil, S. (1998). Phylogeny and PCR-based classification of Wolbachia strains using wsp gene sequences. Proceedings of the Royal Society of London, Series B: Biological Sciences, 265, 509–515.