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We simultaneously considered morphology and molecular phylogeny to modify the generic classification of the ‘pyropterine clade’ (Lycidae, Erotinae, Dictyopterini). To place species previously included in Benibotarus Kôno, 1932 in reciprocally monophyletic genera, we propose Gomezzuritus gen. nov. with the type-species Dictyopterus alternatus Fairmaire, 1856. Further, we transfer Gomezzuritus alternatus (Fairmaire, 1856) comb. nov., G. longicornis (Reiche, 1878) comb. nov., and G. rubripes (Pic, 1897) comb. nov. from Benibotarus to Gomezzuritus gen. nov. The pyropterine clade contains five genera in the Palaearctic region: Pyropterus Mulsant, 1838, Gomezzuritus gen. nov., Helcophorus Fairmaire, 1891, Greenarus Kazantsev, 1995, and Benibotarus Kôno, 1932. The arrangement of longitudinal elytral costae proved misleading for consideration of relationships. Two genera in distant positions share only four primary costae (Pyropterus and Helcophorus), and three similarly distant genera share the shortened primary costa 3, resulting in three primary and four secondary longitudinal costae (Gomezzuritus, Greenarus, and Benibotarus). The larva of Gomezzuritus alternatus is described in detail, and it is compared with the larvae of other Dictyopterini, including the presumed larva of G. longicornis.
This document describes the biological cycle of two species of the genus Corades Doubleday, C. chelonis Hewitson and C. dymantis Thieme. The morphological characteristics of the two species are compared to each other, to other species of Corades and to other members of the subtribe Pronophilina. An outstanding character of the larvae of C. chelonis is the united cephalic horns which differ from the other species of Corades. The hostplant of both species is Chusquea serrulata. Oviposition varies between the two species of the study. Immature stage development takes an average of 147 days for C. chelonis and 150 days for C. dymantis. Both species were raised ex situm in the same life zone. Ethological aspects of the larvae and adults are discussed and compared.
A cladistic analysis is presented of the hawkmoths of the tribe Acherontiini, Morgan´s Sphinx (Xanthopan morganii (Walker», and related genera. The study aims to test the monophyly of tribe Acherontiini; the hypothesis that all taxa with extremely long probosces (some Acherontiini, Meganoton rubescens, Neococytius, Xanthopan) form a monophyletic group, or at least fall within a single reasonably compact clade; and, within this group, to determine whether Xanthopan is more closely related to Acherontiini or to COCytillS and Neococytius. The data set comprises 109 characters derived from adult and immature stage morphology, biology and behaviour. These data were analysed using equal weighting, successive approximations character weighting (SACW) and implied weighting. All weighting schemes agreed on the monophyly of Acherontiini and of a group of genera comprising Amphimoea, Cocytius and Neococytius (the Cocytius group). Several other generic and suprageneric clades were also consistently recovered. However, those hawkmoths with extremely long probosces were never recovered as a monophyletic group. The relationships of Xanthopan were also ambiguous. Equal weighting and SACW placedXanthopan + Meganoton rztbescens (Butler) as sister to the COCytills group, while implied weighting placed Xanthopan as sister to Acherontiini. This latter relationship is based primarily on shared possession of a pilifer/palp hearing organ. Further analyses suggested the two components of this organ were not biologically independent. Downweighting this feature accordingly resulted in all weighting schemes converging on the topology found by equal weighting. Exclusion of the incomplete subset of immature stage data had no effect under implied weighting but equal weighting and SACW now recovered a Neotropical clade comprising Manduca. and the Cocytius group, while Xanthopan was placed with M. rubescens and Panogena. Downweighting the pilifer/palp hearing organ under implied weighting again caused convergence with the equal weighting/SACW results. Thus, the relationships of Xanthopan remain equivocal and further data, particularly from the immature stages, will be required to elucidate its phylogenetic position further.