Lincoln, G. A. Teeth, horns and antlers: the weapons of sex. In The Differences between the Sexes (eds R. V. Short & E. Balaban) 131–158 (Cambridge Univ. Press, 1994).
Lundrigan, B. Morphology of horns and fighting behavior in the family bovidae. J. Mammal. 77, 462–475 (1996).
Google Scholar
Bro-Jorgensen, J. The intensity of sexual selection predicts weapon size in male bovids. Evolution 61, 1316–1326 (2007).
Google Scholar
Plard, F., Bonenfant, C. & Gaillard, J. M. Revisiting the allometry of antlers among deer species: male-male sexual competition as a driver. Oikos 120, 601–606 (2011).
Google Scholar
Okada, K. & Miyatake, T. Sexual dimorphism in mandibles and male aggressive behavior in the presence and absence of females in the beetle Librodor japonicus (Coleoptera: Nitidulidae). Ann. Entomol. Soc. Am. 97, 1342–1346 (2004).
Google Scholar
Emlen, D. J., Marangelo, J., Ball, B. & Cunningham, C. W. Diversity in the weapons of sexual selection: Horn evolution in the beetle genus Onthophagus (Coleoptera: Scarabaeidae). Evolution 59, 1060–1084 (2005).
Google Scholar
Pomfret, J. C. & Knell, R. J. Sexual selection and horn allometry in the dung beetle Euoniticellus intermedius. Anim. Behav. 71, 567–576 (2006).
Google Scholar
McCullough, E. L., Weingarden, P. R. & Emlen, D. J. Costs of elaborate weapons in a rhinoceros beetle: how difficult is it to fly with a big horn?. Behav. Ecol. 23, 1042–1048 (2012).
Google Scholar
David, P., Bjorksten, T., Fowler, K. & Pomiankowski, A. Condition-dependent signalling of genetic variation in stalk-eyes flies. Nature 406, 186–188 (2000).
Google Scholar
Baker, R. H. & Wilkinson, G. S. Phylogenetic analysis of sexual dimorphism and eye-span allometry in stalk-eyed flies (Diopsidae). Evolution 55, 1373–1385 (2001).
Google Scholar
Stankowich, T. Armed and dangerous: predicting the presence and function of defensive weaponry in mammals. Adapt. Behav. 20, 32–43 (2012).
Google Scholar
Hashimoto, K. & Hayashi, F. Structure and function of the large pronotal horn of the sand-living anthicid beetle Mecynotarsus tenuipes. Entomol. Sci. 15, 274–279 (2012).
Google Scholar
Hayashi, M. & Ohba, S. Y. Mouth morphology of the diving beetle Hyphydrus japonicus (Dytiscidae: Hydroporinae) is specialized for predation on seed shrimps. Biol. J. Linn. Soc. 125, 315–320 (2018).
Google Scholar
Stocker, R. F. The organization of the chemosensory system in Drosophila melanogaster: a review. Cell Tissue Res. 275, 3–26 (1994).
Google Scholar
Dweck, H. K. M. Antennal sensory receptors of Pteromalus puparum female (Hymenoptera: Pteromalidae), a gregarious pupal endoparasitoid of Pieris rapae. Micron 40, 769–774 (2009).
Google Scholar
Crespo, J. G. A review of chemosensation and related behavior in aquatic insects. J. Insect Sci. 11, 1–39 (2011).
Google Scholar
Stoffolano, J. G. Jr., Rice, M. & Murphy, W. L. The importance of antennal mechanosensilla of Sepedon fuscipennis (Diptera: Sciomyzidae). Can. Entomol. 145, 265–272 (2013).
Google Scholar
Gabel, B. et al. Floral volatiles of Tanacetum vulgare L. attractive to Lobesia botrana Den. et Schiff. females. J. Chem. Ecol. 18, 693–701 (1992).
Google Scholar
Fox, H. Barbels and barbel-like tentacular structures in sub-mammalian vertebrates: a review. Hydrobiologia 403, 153–193 (1999).
Google Scholar
Plepys, D., Ibarra, F., Francke, W. & Lofstedt, C. Odour-mediated nectar foraging in the silver Y moth, Autographa gamma (Lepidoptera: Noctuidae): behavioural and electrophysiological responses to floral volatiles. Oikos 99, 75–82 (2002).
Google Scholar
Stankowich, T. & Caro, T. Evolution of weaponry in female bovids. Proc. R. Soc. Lond. Ser. B Biol. Sci. 276, 4329–4334 (2009).
Bergmann, P. J. & Berk, C. P. The Evolution of Positive Allometry of Weaponry in Horned Lizards (Phrynosoma). Evol. Biol. 39, 311–323 (2012).
Google Scholar
Damman, H. The osmaterial glands of the swallowtail butterfly Eurytide marcellus as a defense against natural enemies. Ecol. Entomol. 11, 261–265 (1986).
Google Scholar
Berenbaum, M. R., Moreno, B. & Green, E. Soldier bug predation on swallowtail caterpillars (Lepidoptera, Papilionidae): circumvention of defensive chemistry. J. Insect Behav. 5, 547–553 (1992).
Google Scholar
Juma, G. et al. Distribution of chemo- and mechanoreceptors on the antennae and maxillae of Busseola fusca larvae. Entomol. Exp. Appl. 128, 93–98 (2008).
Google Scholar
Liu, Z., Hua, B.-Z. & Liu, L. Ultrastructure of the sensilla on larval antennae and mouthparts in the peach fruit moth, Carposina sasakii Matsumura (Lepidoptera: Carposinidae). Micron 42, 478–483 (2011).
Google Scholar
Kandori, I., Tsuchihara, K., Suzuki, T. A., Yokoi, T. & Papaj, D. R. Long frontal projections help Battus philenor (Lepidoptera: Papilionidae) larvae find host plants. PLoS ONE 10, e0131596 (2015).
Google Scholar
Greeney, H. F., Dyer, L. A. & Smilanich, A. M. Feeding by lepidopteran larvae is dangerous: A review of caterpillars’ chemical, physiological, morphological, and behavioral defenses against natural enemies. ISJ Invert. Surviv. J. 9, 7–34 (2012).
Sugiura, S. Predators as drivers of insect defenses. Entomol. Sci. 23, 316–337 (2020).
Google Scholar
Martin, W. R. & Nordlund, D. A. Ovipositional behavior of the parasitoid Palexorista laxa (Diptera, Tachinidae) on Heliothis zea (Lepidoptera, Noctuidae) larvae. J. Entomol. Sci. 24, 460–464 (1989).
Google Scholar
Constantino, L. M. Notes on Haetera from Colombia, with description of the immature stages of Haetera piera (Lepidoptera:Nymphalidae: Satyrinae). Trop. Lepid. 4(1), 13–15 (1993).
Devries, P. J., Kitching, I. J. & Vanewright, R. I. The systematic position of Antirrhea and Caerois, with comments on the classification of the Nymphalidae (Lepidoptera). Syst. Entomol. 10, 11–32. https://doi.org/10.1111/j.1365-3113.1985.tb00561.x (1985).
Google Scholar
Dias, F. M. S., Casagrande, M. M. & Mielke, O. H. H. Biology and external morphology of immature stages of Memphis appias (Hubner) (Lepidoptera: Nymphalidae: Charaxinae). Zootaxa, 21–32 (2010).
Dias, F. M. S., Casagrande, M. M. & Mielke, O. H. H. Biology and external morphology of the immature stages of the butterfly Callicore pygas eucale, with comments on the taxonomy of the genus Callicore (Nymphalidae: Biblidinae). J. Insect Sci. 14, doi:https://doi.org/10.1093/jis/14.1.91 (2014).
Dias, F. M. S., Casagrande, M. M. & Mielke, O. H. H. Immature stages of the turquoise-banded shoemaker Archaeoprepona amphimachus pseudomeander (Fruhstorfer, 1906) and a comparative review of the Preponini (Lepidoptera: Nymphalidae). Aust. Entomol. 58, 451–462. https://doi.org/10.1111/aen.12339 (2019).
Google Scholar
Dias, F. M. S., de Oliveira-Neto, J. F., Casagrande, M. M. & Mielke, O. H. H. External morphology of immature stages of Zaretis strigosus (Gmelin) and Siderone galanthis catarina Dottax and Pierre comb. nov., with taxonomic notes on Siderone (Lepidoptera: Nymphalidae: Charaxinae). Rev. Bras. Entomol. 59, 307–319, doi:https://doi.org/10.1016/j.rbe.2015.07.007 (2015).
Dias, F. M. S. et al. An integrative approach elucidates the systematics of Sea Hayward and Cybdelis Boisduval (Lepidoptera: Nymphalidae: Biblidinae). Syst. Entomol. 44, 226–250. https://doi.org/10.1111/syen.12327 (2019).
Google Scholar
Freitas, A. V. L., Barbosa, E. P. & Marin, M. A. Immature Stages and Natural History of the Neotropical Satyrine Pareuptychia ocirrhoe Interjecta (Nymphalidae: Euptychiina). J. Lepid. Soc. 70, 271–276. https://doi.org/10.18473/lepi.70i4.a4 (2016).
Google Scholar
Freitas, A. V. L., Kaminski, L. A., Mielke, O. H. H., Barbosa, E. P. & Silva-Brandao, K. L. A new species of Yphthimoides (Lepidoptera: Nymphalidae: Satyrinae) from the southern Atlantic forest region. Zootaxa, 31–44 (2012).
Furtado, E. & Campos-Neto, F. C. Caligopsis seleucida (Hewitson) and its immature stages (Lepidoptera, Nymphalidae, Brassolinae). Rev. Bras. Zool. 21(3), 593–597 (2004).
Google Scholar
Greeney, H. F. et al. The early stages and natural history of Antirrhea adoptiva porphyrosticta (Watkins, 1928) in eastern Ecuador (Lepidoptera: Nymphalidae: Morphinae). J. Insect Sci. 9 (2009).
Greeney, H. F. et al. Early stages and natural history of Perisama oppelii (Nymphalidae, Lepidoptera) in eastern Ecuador. Kempffiana 6(1), 16–30 (2010).
Greeney, H. F., Dyer, L. A. & Pyrcz, T. W. First description of the early stage biology of the genus Mygona: The natural history of the satyrine butterfly, Mygona irmina in eastern Ecuador. J. Insect Sci. 11, doi:https://doi.org/10.1673/031.011.0105 (2011).
Greeney, H. F., Pyrcz, T. W., DeVries, P. J. & Dyer, L. A. The early stages of Pedaliodes poesia (Hewitson, 1862) in eastern Ecuador (Lepidoptera: Satyrinae: Pronophilina). J. Insect Sci. 9 (2009).
Greeney, H. F., Whitfield, J. B., Stireman, J. O., Penz, C. M. & Dyer, L. A. Natural history of Eryphanis greeneyi (Lepidoptera: Nymphalidae) and its enemies, with a description of a new species of Braconid parasitoid and notes on its Tachinid parasitoid. Ann. Entomol. Soc. Am. 104, 1078–1090. https://doi.org/10.1603/an10064 (2011).
Google Scholar
Kaminski, L. A. & Freitas, A. V. L. Immature stages of the butterfly Magneuptychia libye (L.) (Lepidoptera : Nymphalidae, Satyrinae). Neotrop. Entomol. 37, 169–172, doi:https://doi.org/10.1590/s1519-566×2008000200010 (2008).
Lambkin, T. & Kendall, R. The status of Yoma algina (boisduval, 1832) & Y. sabina (cramer, 1780) (Lepidoptera: Nymphalidae: Nymphalinae) in Australia. Aust. Entomol. 43 (4), 211–234 (2016).
Leite, L. A. R., Casagrande, M. M., Mielke, O. H. H. & Freitas, A. V. L. Immature stages of the Neotropical butterfly, Dynamine agacles agacles. J. Insect Sci. 12 (2012).
Leite, L. A. R., Dias, F. M. S., Carneiro, E., Casagrande, M. M. & Mielke, O. H. H. Immature stages of the Neotropical cracker butterfly, Hamadryas epinome. J. Insect Sci. 12 (2012).
Murillo, L. R. & Nishida, K. Life history of Manataria maculata (Lepidoptera : Satyrinae) from Costa Rica. Rev. Biol. Trop. 51, 463–469 (2003).
Google Scholar
Nakahara, S., Janzen, D. H., Hallwachs, W. & Espeland, M. Description of a new genus for Euptychia hilara (C. Felder & R. Felder, 1867) (Lepidoptera: Nymphalidae: Satyrinae). Zootaxa 4012, 525-541, doi:https://doi.org/10.11646/zootaxa.4012.3.7 (2015).
Penz, C. M., Freitas, A. V. L., Kaminski, L. A., Casagrande, M. M. & Devries, P. J. Adult and early-stage characters of Brassolini contain conflicting phylogenetic signal (Lepidoptera, Nymphalidae). Syst. Entomol. 38, 316–333. https://doi.org/10.1111/syen.12000 (2013).
Google Scholar
Pyrcz, T. W. et al. Uncovered diversity of a predominantly Andean butterfly clade in the Brazilian Atlantic forest: a revision of the genus Praepedaliodes Forster (Lepidoptera: Nymphalidae, Satyrinae, Satyrini). Neotrop. Entomol. 47, 211–255. https://doi.org/10.1007/s13744-017-0543-x (2018).
Google Scholar
Shirai, L. T. et al. Natural history of Selenophanes cassiope guarany (Lepidoptera: Nymphalidae: Brassolini): an integrative approach, from molecules to ecology. Ann. Entomol. Soc. Am. 110, 145–159. https://doi.org/10.1093/aesa/saw068 (2017).
Google Scholar
Silva, P. L. et al. Immature Stages of the Brazilian Crescent Butterfly Ortilia liriope (Cramer) (Lepidoptera: Nymphalidae). Neotrop. Entomol. 40, 322–327. https://doi.org/10.1590/s1519-566×2011000300006 (2011).
Google Scholar
Song-yun, L. Immature stages of Faunis aerope (Leech, 1890) (Lepidoptera, Nymphalidae). Atalanta 42, 221–222 (2011).
Steiner, H. Life history of Melanocyma faunula in Malaysia (Lepidoptera: Nymphalidae: Morphinae). Trop. Lepid. Res. 16, 23–26 (2005).
Velez, P. D., Montoya, H. H. V. & Wolff, M. Immature stages and natural history of the Andean butterfly Altinote ozomene (Nymphalidae: Heliconiinae: Acraeini). Zoologia 28, 593–602. https://doi.org/10.1590/s1984-46702011000500007 (2011).
Google Scholar
Wahlberg, N. et al. Nymphalid butterflies diversify following near demise at the Cretaceous/Tertiary boundary. Proc. R. Soc. Lond. Ser. B Biol. Sci. 276, 4295–4302, doi:https://doi.org/10.1098/rspb.2009.1303 (2009).
Willmott, K. R., Elias, M. & Sourakov, A. Two possible caterpillar mimicry complexes in neotropical Danaine butterflies (Lepidoptera: Nymphalidae). Ann. Entomol. Soc. Am. 104, 1108–1118. https://doi.org/10.1603/an10086 (2011).
Google Scholar
Willmott, K. R. & Freitas, A. V. L. Higher-level phylogeny of the Ithomiinae (Lepidoptera : Nymphalidae): classification, patterns of larval hostplant colonization and diversification. Cladistics 22, 297–368. https://doi.org/10.1111/j.1096-0031.2006.00108.x (2006).
Google Scholar
Zacca, T. et al. Revision of Godartiana Forster (Lepidoptera: Nymphalidae), with the description of a new species from northeastern Brazil. Aust. Entomol. 56, 169–190. https://doi.org/10.1111/aen.12223 (2017).
Google Scholar
Bossart, J.L., Fetzner Jr., J.F. & Rawlins, J.E. Ghana Butterfly Biodiversity Project website. https://www.invertebratezoology.org/GhanaBfly/default.asp (2007).
Butterflies and Moths of North America project. Butterflies and Moths of North America website. https://www.butterfliesandmoths.org/ (2021).
Dauphin, D. & Dauphin, J. The Rio Grande Valley’s Nature Site website. http://www.thedauphins.net (2021).
Eeles, P. UK Butterflies website. https://www.ukbutterflies.co.uk/index.php. (2021).
Florida Museum of Natural History. Florida Museum website. https://www.floridamuseum.ufl.edu/ (2021).
Khew, S. K. et al. Butterflies of Singapore website. https://butterflycircle.blogspot.com/ (2021).
Kunte, K., Sondhi, S. & Roy, P. Butterflies of India, v. 3.24. Indian Foundation for Butterflies website. https://www.ifoundbutterflies.org (2021).
Miller, S. & Morrison, C. Parasitoid-Caterpillar-Plant Interactions in the Americas website. https://caterpillars.myspecies.info/ (2021).
National Biodiversity Network Trust. iNaturalistUK website. https://uk.inaturalist.org/ (2021).
Nature Picture Library Limited. Nature Picture Library website. https://www.naturepl.com/blog/ (2021).
Project Noah Team. Project Noah website. https://www.projectnoah.org/ (2021).
Shiraiwa, K. Pteron World. The encyclopedia website of the butterflies. https://www.pteron-world.com/index.html (2021).
Wagner, W. Lepidoptera and Their Ecology website. http://www.pyrgus.de/ (2021).
Wahlberg, N. & Peña, C. Nymphalidae.net. website. http://www.nymphalidae.net/ (2021).
Wikimedia Foundation, Inc. Wikimedia Commons website. https://commons.wikimedia.org/ (2021).
Matsuura, M. Social Wasps of Japan in Color. (in Japanese) (Hokkaido university press 2015).
IBM SPSS. SPSS Base 25.0 User’s Guide. (SPSS Inc., 2017).
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