Taxonomic Status and Redescription of Magneuptychia
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Zootaxa, Guaianaza for "Yuptychia" Pronophila (Lepidoptera: Nymphalidae: Satyrinae)
Zootaxa 1163: 49–59 (2006) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1163 Copyright © 2006 Magnolia Press ISSN 1175-5334 (online edition) Description of Genus Guaianaza for “Euptychia” pronophila (Lepidoptera: Nymphalidae: Satyrinae) with a description of the immature stages ANDRÉ VICTOR LUCCI FREITAS1 & CARLOS PEÑA2 1Departamento de Zoologia and Museu de História Natural, Instituto de Biologia, Universidade Estadual de Campinas, CP 6109, Campinas, São Paulo 13083-970, Brazil, [email protected] 2Department of Zoology, Stockholm University S-106 91, Stockholm, Sweden, [email protected] Abstract The satyrine Euptychia pronophila Butler (Nymphalidae) was described in 1867 in the “catch-all” genus Euptychia, but was recently treated as incertae sedis. A DNA-based cladistic analysis con- firms that it belongs to the Euptychiina, as sister to Forsterinaria and closely related to Taygetis, Posttaygetis, Parataygetis, Pseudodebis, and Harjesia. Although immature morphology also sug- gests that this species is closely related to Forsterinaria, none of the adult morphological synapo- morphies for the genera in the aforementioned clade occur in E. pronophila, a highly autapomorphic species. Because we were unable to place it with confidence in an established genus, the monotypic satyrine genus Guaianaza Freitas & Peña New Genus is described, with Eup- tychia pronophila Butler as the type species. Key words: Atlantic forest, Forsterinaria, life history, Neotropics, Poaceae. Introduction The butterfly family Nymphalidae is composed of about 7200 species distributed through- out the world (Ackery et al. 1999). Nymphalid species exhibit a great variety of color pat- terns and morphological features, but are united by the synapomorphy of “tricarinate” antennae (Vane-Wright 2003). -
Lycaenidae: Theclinae: Eumaeini)
Nomenclature, variation, and the biological species concept in Lamasina (Lycaenidae: Theclinae: Eumaeini) Robert K. Robbins1 & Gerardo Lamas2 1 Department of Entomology, Smithsonian Institution. PO Box 37012, NHB Stop 105, Washington, DC 20013-7012 USA. E-mail: [email protected] 2 Museo de Historia Natural, Universidad Nacional Mayor de San Marcos. Apartado 14-0434, Lima-14, Peru. E-mail: [email protected] ABSTRACT. The correct generic name for the species that belong to Eucharia Boisduval, 1870, a homonym, is either Annamaria D’Abrera & Bálint, 2001, which has been considered to be unavailable, or Lamasina Robbins, 2002, a replacement name for Eucharia. A recent re-interpretation of the original description of Annamaria was incorrect, and Annamaria is confirmed as being unavailable under Article 13.1 of the Code. A proposed neotype for Papilio ganimedes Cramer, 1775 is invalidated, and a possible syntype is illustrated. Results of an analysis of variation in the Lamasina ganimedes complex are distinctly different from those previously published and provide insufficient evidence to support the hypothesis that L. lathyi (Bálint, 2005) is distinct under a biological species concept. Lamasina lathyi is a synonym of L. ganimedes syn. nov. Statistical evidence overwhelmingly falsifies the published hypothesis that the L. rhaptissima (Johnson, 1991) (14 males) and L. columbia (Bálint, 2005) (8 females) species complexes are distinct rather than males and females of the same complex. Lamasina columbia is endemic to western Colombia. The hypothesis that L. rhapsodia (Bálint, 2005) from Bolivia is a distinct species is not better supported than the hypotheses that the one known specimen of L. -
And Evenus Batesii (Hewitson) (Lepidoptera: Lycaenidae)
Bioma, enero de 2013 Laboratory breeding of the “Living Jewels” of El Salvador, Evenus regalis (Cramer) and Evenus batesii (Hewitson) (Lepidoptera: Lycaenidae) Sermeño-Chicas, J.M. Profesor of Entomology, Chief of Research Directorate, Faculty of Agronomic Sciences, University of El Salvador. El Salvador, C.A. E-mail: [email protected] Robbins, R.K. Research Entomologist , Smithsonian Institution, Washington, USA. E-mail: [email protected] Lamas, G. Department of Entomology, Natural History Museum, Universidad Nacional Mayor de San Marcos. Peru. E-mail: [email protected] Gámez-Alas, J.A. The neotropical genus Evenus Hübner (Lycaenidae: Sapotaceae: sapote (Pouteria sapota (Jacq.) H. E. Moore & iridescent green, red, and purple with black stripes, which Eumaeini) of butterflies occurs from Mexico to southern Stearn), and caimito (Chrysophyllum cainito L.) (Sermeño, make them be named as “living jewels” (Fig. 1a, c and 2b). Brazil, mainly in lowland forests and contains 12 species 2009). The field collection and laboratory breeding of the In adults, the maxillary palps are absent and labial palps are (Robbins, 2004b). Evenus is characterized (Robbins, immature stages of this species began in 2006, proving well developed. In the hindwings, the CuA2 vein projects 2004a) by its unique androconial structures, their for several years that the females lay eggs in the wild in into a long tail. Salvadoran male specimens have been reproductive organs and because its larvae feed on plants the tender shoots of host plants from May to October, found to have two long tails and two short tails (Fig. 1a-c), of the family Sapotaceae which is unique within the observing that, depending on the quality and availability of while in females both tails are long (Fig 2a, b). -
In Northern Chile, with Notes on Palmaris Penai (Hayward, 1967) (Lepidoptera, Nymphalidae, Satyrinae)
Boletín Sociedad Entomológica Aragonesa, nº 44 (2009) : 351–356. PRESENCE AND PHENOTYPIC VARIABILITY OF PALMARIS GUSTAVI (STAUDINGER, 1898) IN NORTHERN CHILE, WITH NOTES ON PALMARIS PENAI (HAYWARD, 1967) (LEPIDOPTERA, NYMPHALIDAE, SATYRINAE) Juan Modolell1, Miguel L. Munguira2 & Enrique García-Barros2 1Centro de Biología Molecular Severo Ochoa, CSIC and Universidad Autónoma de Madrid, 28049 Madrid, Spain. – at jmo- [email protected] 2Depto. de Biología (Zoología), Universidad Autónoma de Madrid, 28049 Madrid, Spain. Abstract: Although it has been assumed that the satyrine butterfly Palmaris gustavi (Staudinger, 1898) should be present in northern Chile, no reliable reports of its observation and capture have been provided. Here, we report the presence of P. gusta- vi in several localities of northern Chile stretching from the altiplanic regions of Putre to those of San Pedro de Atacama, 550 km to the south. We also report that this butterfly displays a strong phenotypic variability, ranging from dark forms with entirely dark brown upper wing surfaces to light forms with large silvery discal and marginal areas. Both forms were observed together in one population. Illustrations of the adult habitus and male genitalia are provided, as well as notes and illustrations of the habi- tat. We suggest that the closely related Palmaris penai (Hayward, 1967) may be conspecific with P. gustavi, or alternatively that the San Pedro de Atacama population observed by us represents P. penai and the diagnostic features of this species have to be reassessed. Key words: Lepidoptera, Nymphalidae, Satyrinae, Palmaris gustavi, Palmaris penai, northern Chile. Presencia y variabilidad fenotípica de Palmaris gustavi (Staudinger, 1898) en el norte de Chile y notas sobre Palmaris penai (Hayward, 1967) (Lepidoptera, Nymphalidae, Satyrinae) Resumen: Aunque se sospechaba que el satirino Palmaris gustavi (Staudinger, 1898) debería encontrarse en el norte de Chi- le, no se conocían datos fidedignos de su observación y captura. -
Systematics, Bionomics and Zoogeography of High Andean
Genus Vol. 19(3): 471-495 Wrocław, 30 X 2008 Systematics, bionomics and zoogeography of high Andean pedaliodines; Part 10: Revisional notes on Pedaliodes tyro THIEME with the description of new allied taxa from central and southern Peru (Lepidoptera: Nymphalidae: Satyrinae) TOMASZ W. PYRCZ1, ANGEL. L. VILORIA2, PIERRE BOYER3 & GERARDO LAMAS4 1Zoological Museum of the Jagiellonian University, Ingardena 6, 30-060 Kraków, Poland, [email protected] 2Centro de Ecología, Instituto Venezolano de Investigaciones Científicas, Apartado 20632, Caracas 1020-A, Venezuela, [email protected] 3Lotissement l’Horizon, 13610 Le Puy Sainte Réparade, France, [email protected] 4Museo de Historia Natural de la Universidad Nacional Mayor de San Marcos, Av. Arenales 1256, Lima, Peru, [email protected] ABSTRACT. Eight new taxa related to Pedaliodes tyro THIEME are described, including six species and two subspecies. It is demonstrated that the designation of the lectotype of Pedaliodes tyro from Marcapata is incorrect, and that the true type locality is Limbani. P. tyro is redescribed and redefined. Key words: entomology, taxonomy, Satyrinae, Pedaliodes, new taxa, redescription, Andes. INTRODUCTION Pedaliodes BUTLER (Nymphalidae, Satyrinae, Satyrini) is the most speciose genus of the Neotropical butterflies with at least 200 currently recognised species L( AMAS et al. 2004). This large number of taxa often does not translate into morphological diversity, especially the wing colour patterns. Several basic elements are found in almost every single taxon. For example, the hindwing underside, in the absence of other prominent colour patterns, usually possess a yellow, orange or reddish triangular or elongate anal wedge and a usually short costal streak. There are dozens of species with these markings, often several sympatric, and their correct identification requires more thorough morphological study, including the comparing of male androconial 472 TOMASZ W. -
INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a Synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a Historical Sketch
ZOOLOGÍA-TAXONOMÍA www.unal.edu.co/icn/publicaciones/caldasia.htm Caldasia 31(2):407-440. 2009 HACIA UNA SÍNTESIS DE LOS PAPILIONOIDEA (INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a historical sketch JOSÉ LUIS SALINAS-GUTIÉRREZ El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] CLAUDIO MÉNDEZ Escuela de Biología, Universidad de San Carlos, Ciudad Universitaria, Campus Central USAC, Zona 12. Guatemala, Guatemala. [email protected] MERCEDES BARRIOS Centro de Estudios Conservacionistas (CECON), Universidad de San Carlos, Avenida La Reforma 0-53, Zona 10, Guatemala, Guatemala. [email protected] CARMEN POZO El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] JORGE LLORENTE-BOUSQUETS Museo de Zoología, Facultad de Ciencias, UNAM. Apartado Postal 70-399, México D.F. 04510; México. [email protected]. Autor responsable. RESUMEN La riqueza biológica de Mesoamérica es enorme. Dentro de esta gran área geográfi ca se encuentran algunos de los ecosistemas más diversos del planeta (selvas tropicales), así como varios de los principales centros de endemismo en el mundo (bosques nublados). Países como Guatemala, en esta gran área biogeográfi ca, tiene grandes zonas de bosque húmedo tropical y bosque mesófi lo, por esta razón es muy importante para analizar la diversidad en la región. Lamentablemente, la fauna de mariposas de Guatemala es poco conocida y por lo tanto, es necesario llevar a cabo un estudio y análisis de la composición y la diversidad de las mariposas (Lepidoptera: Papilionoidea) en Guatemala. -
Butterflies (Lepidoptera: Papilionoidea) in a Coastal Plain Area in the State of Paraná, Brazil
62 TROP. LEPID. RES., 26(2): 62-67, 2016 LEVISKI ET AL.: Butterflies in Paraná Butterflies (Lepidoptera: Papilionoidea) in a coastal plain area in the state of Paraná, Brazil Gabriela Lourenço Leviski¹*, Luziany Queiroz-Santos¹, Ricardo Russo Siewert¹, Lucy Mila Garcia Salik¹, Mirna Martins Casagrande¹ and Olaf Hermann Hendrik Mielke¹ ¹ Laboratório de Estudos de Lepidoptera Neotropical, Departamento de Zoologia, Universidade Federal do Paraná, Caixa Postal 19.020, 81.531-980, Curitiba, Paraná, Brazil Corresponding author: E-mail: [email protected]٭ Abstract: The coastal plain environments of southern Brazil are neglected and poorly represented in Conservation Units. In view of the importance of sampling these areas, the present study conducted the first butterfly inventory of a coastal area in the state of Paraná. Samples were taken in the Floresta Estadual do Palmito, from February 2014 through January 2015, using insect nets and traps for fruit-feeding butterfly species. A total of 200 species were recorded, in the families Hesperiidae (77), Nymphalidae (73), Riodinidae (20), Lycaenidae (19), Pieridae (7) and Papilionidae (4). Particularly notable records included the rare and vulnerable Pseudotinea hemis (Schaus, 1927), representing the lowest elevation record for this species, and Temenis huebneri korallion Fruhstorfer, 1912, a new record for Paraná. These results reinforce the need to direct sampling efforts to poorly inventoried areas, to increase knowledge of the distribution and occurrence patterns of butterflies in Brazil. Key words: Atlantic Forest, Biodiversity, conservation, inventory, species richness. INTRODUCTION the importance of inventories to knowledge of the fauna and its conservation, the present study inventoried the species of Faunal inventories are important for providing knowledge butterflies of the Floresta Estadual do Palmito. -
Magneuptychia Flavofascia Zacca & Siewert, 2014 (Lepidoptera: Nymphalidae)
11 4 1692 the journal of biodiversity data 13 July 2015 Check List NOTES ON GEOGRAPHIC DISTRIBUTION Check List 11(4): 1692, 13 July 2015 doi: http://dx.doi.org/10.15560/11.4.1692 ISSN 1809-127X © 2015 Check List and Authors New distribution records and notes on the habitat of Magneuptychia flavofascia Zacca & Siewert, 2014 (Lepidoptera: Nymphalidae) Lucas A. Kaminski1, 2*, Rafael Dell’Erba3, Eduardo P. Barbosa2 and André V. L. Freitas2 1 Institut de Biologia Evolutiva (CSIC-UPF), Passeig Marítim de la Barceloneta, 37, 08003 Barcelona, Spain 2 Departamento de Biologia Animal and Museu de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, CP 6109, 13083- 970, Campinas, SP, Brazil 3 Museu de Zoologia da Universidade de São Paulo, Avenida Nazaré 481, Ipiranga, 04263–000, São Paulo, SP, Brazil * Corresponding author. E-mail: [email protected] Abstract: The recently described butterfly Magneu The species was studied in the field at Parque Nacional ptychia flavofascia was formerly known from only two da Chapada dos Guimarães (PNCG), Chapada dos localities in the Brazilian Cerrado savanna. Here, we re- Guimarães municipality, Mato Grosso state, Brazil. The port new distribution records, DNA barcode sequences, park contains almost all Cerrado physiognomies, with and information on the habitat, adult behavior and sys- altitudes ranging from 200 to 900 m (for details see Pinto tematic position of this species. and Oliveira-Filho 1999). The study was carried out along two different trails, 5 km long, each containing three Key words: Chapada dos Guimarães, DNA barcoding, sampling units, 2 km apart. Each sampling unit consisted grassland butterflies, Paryphthimoides, Satyrinae of five portable bait traps (see Uehara-Prado et al. -
A Distinctive New Species of Cloud Forest Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from Ecuador and Peru
WILLMOTT ET AL.: New species of Erichthodes TROP. LEPID. RES., 28(1): 39-45, 2018 39 A distinctive new species of cloud forest Euptychiina (Lepidoptera: Nymphalidae: Satyrinae) from Ecuador and Peru Keith R. Willmott1, Gerardo Lamas2, James Radford3, Mario A. Marín4, Shinichi Nakahara1, Marianne Espeland5, Lei Xiao1, and Jason P. W. Hall6 1. McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL, USA: [email protected] 2. Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Lima, Peru. 3. Cambridge, UK. 4. Departamento de Biologia Animal and Museu de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, Rua Monteiro Lobato, 255 - Cidade Universitária Zeferino Vaz - Barão Geraldo, 13083-862, Campinas, São Paulo, Brazil. 5. Arthropoda Department, Zoological Research Museum Alexander Koenig, Adenauer Allee 160, 53113 Bonn, Germany. 6. Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, USA Date of issue online: 13 July 2018 Zoobank Registered: urn:lsid:zoobank.org:pub:F4A0F8EB-600F-4973-9D52-DDA7E27C3EF8 Electronic copies (ISSN 2575-9256) in PDF format at: http://journals.fcla.edu/troplep; https://zenodo.org; archived by the Institutional Repository at the University of Florida (IR@UF), http://ufdc.ufl.edu/ufir;DOI : 10.5281/zenodo.1309677 © The author(s). This is an open access article distributed under the Creative Commons license CC BY-NC 4.0 (https://creativecommons.org/ licenses/by-nc/4.0/). Abstract: A new species of Euptychiina, Erichthodes eremita Lamas, Willmott & Radford, n. sp., is described and illustrated. DNA sequence data suggest that the new species is sister to a species currently placed in Erichthodes Forster, 1964, although ongoing revision of the generic taxonomy of the subtribe might result in the reclassification of both of these species in future. -
The Radiation of Satyrini Butterflies (Nymphalidae: Satyrinae): A
Zoological Journal of the Linnean Society, 2011, 161, 64–87. With 8 figures The radiation of Satyrini butterflies (Nymphalidae: Satyrinae): a challenge for phylogenetic methods CARLOS PEÑA1,2*, SÖREN NYLIN1 and NIKLAS WAHLBERG1,3 1Department of Zoology, Stockholm University, 106 91 Stockholm, Sweden 2Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Av. Arenales 1256, Apartado 14-0434, Lima-14, Peru 3Laboratory of Genetics, Department of Biology, University of Turku, 20014 Turku, Finland Received 24 February 2009; accepted for publication 1 September 2009 We have inferred the most comprehensive phylogenetic hypothesis to date of butterflies in the tribe Satyrini. In order to obtain a hypothesis of relationships, we used maximum parsimony and model-based methods with 4435 bp of DNA sequences from mitochondrial and nuclear genes for 179 taxa (130 genera and eight out-groups). We estimated dates of origin and diversification for major clades, and performed a biogeographic analysis using a dispersal–vicariance framework, in order to infer a scenario of the biogeographical history of the group. We found long-branch taxa that affected the accuracy of all three methods. Moreover, different methods produced incongruent phylogenies. We found that Satyrini appeared around 42 Mya in either the Neotropical or the Eastern Palaearctic, Oriental, and/or Indo-Australian regions, and underwent a quick radiation between 32 and 24 Mya, during which time most of its component subtribes originated. Several factors might have been important for the diversification of Satyrini: the ability to feed on grasses; early habitat shift into open, non-forest habitats; and geographic bridges, which permitted dispersal over marine barriers, enabling the geographic expansions of ancestors to new environ- ments that provided opportunities for geographic differentiation, and diversification. -
Amphiesmeno- Ptera: the Caddisflies and Lepidoptera
CY501-C13[548-606].qxd 2/16/05 12:17 AM Page 548 quark11 27B:CY501:Chapters:Chapter-13: 13Amphiesmeno-Amphiesmenoptera: The ptera:Caddisflies The and Lepidoptera With very few exceptions the life histories of the orders Tri- from Old English traveling cadice men, who pinned bits of choptera (caddisflies)Caddisflies and Lepidoptera (moths and butter- cloth to their and coats to advertise their fabrics. A few species flies) are extremely different; the former have aquatic larvae, actually have terrestrial larvae, but even these are relegated to and the latter nearly always have terrestrial, plant-feeding wet leaf litter, so many defining features of the order concern caterpillars. Nonetheless, the close relationship of these two larval adaptations for an almost wholly aquatic lifestyle (Wig- orders hasLepidoptera essentially never been disputed and is supported gins, 1977, 1996). For example, larvae are apneustic (without by strong morphological (Kristensen, 1975, 1991), molecular spiracles) and respire through a thin, permeable cuticle, (Wheeler et al., 2001; Whiting, 2002), and paleontological evi- some of which have filamentous abdominal gills that are sim- dence. Synapomorphies linking these two orders include het- ple or intricately branched (Figure 13.3). Antennae and the erogametic females; a pair of glands on sternite V (found in tentorium of larvae are reduced, though functional signifi- Trichoptera and in basal moths); dense, long setae on the cance of these features is unknown. Larvae do not have pro- wing membrane (which are modified into scales in Lepi- legs on most abdominal segments, save for a pair of anal pro- doptera); forewing with the anal veins looping up to form a legs that have sclerotized hooks for anchoring the larva in its double “Y” configuration; larva with a fused hypopharynx case. -
Family LYCAENIDAE: 268 Species GOSSAMERWINGS
Family LYCAENIDAE: 268 species GOSSAMERWINGS Subfamily Miletinae: 1 (hypothetical) species Harvesters Feniseca tarquinius tarquinius Harvester Hypothetical, should occur in N Tamaulipas, but currently unknown from Mexico Subfamily Lycaeninae: 6 species Coppers Iophanus pyrrhias Guatemalan Copper Lycaena arota arota Tailed Copper Lycaena xanthoides xanthoides Great Copper Lycaena gorgon gorgon Gorgon Copper Lycaena helloides Purplish Copper Lycaena hermes Hermes Copper Subfamily Theclinae: 236 species Hairstreaks Tribe Theclini: 3 species Hairstreaks Hypaurotis crysalus crysalus Colorado Hairstreak Habrodais grunus grunus Golden Hairstreak verification required for Baja California Norte Habrodais poodiae Baja Hairstreak Tribe Eumaeini: 233 Hairstreaks Eumaeus childrenae Great Cycadian (= debora) Eumaeus toxea Mexican Cycadian Theorema eumenia Pale-tipped Cycadian Paiwarria antinous Felders' Hairstreak Paiwarria umbratus Thick-tailed Hairstreak Mithras sp. undescribed Pale-patched Hairstreak nr. orobia Brangas neora Common Brangas Brangas coccineifrons Black-veined Brangas Brangas carthaea Green-spotted Brangas Brangas getus Bright Brangas Thaeides theia Brown-barred Hairstreak Enos thara Thara Hairstreak Enos falerina Falerina Hairstreak Evenus regalis Regal Hairstreak Evenus coronata Crowned Hairstreak Evenus batesii Bates’ Hairstreak Atlides halesus corcorani Great Blue Hairstreak Atlides gaumeri White-tipped Hairstreak Atlides polybe Black-veined Hairstreak Atlides inachus Spying Hairstreak Atlides carpasia Jeweled Hairstreak Atlides