Refining the Diagnostic Characters and Distribution of Hermeuptychia Intricata (Nymphalidae: Satyrinae: Satyrini)
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Butterflies of the Wesleyan Campus
BUTTERFLIES OF THE WESLEYAN CAMPUS SWALLOWTAILS Hairstreaks (Subfamily - Theclinae) (Family PAPILIONIDAE) Great Purple Hairstreak - Atlides halesus Coral Hairstreak - Satyrium titus True Swallowtails Banded Hairstreak - Satyrium calanus (Subfamily - Papilioninae) Striped Hairstreak - Satyrium liparops Pipevine Swallowtail - Battus philenor Henry’s Elfin - Callophrys henrici Zebra Swallowtail - Eurytides marcellus Eastern Pine Elfin - Callophrys niphon Black Swallowtail - Papilio polyxenes Juniper Hairstreak - Callophrys gryneus Giant Swallowtail - Papilio cresphontes White M Hairstreak - Parrhasius m-album Eastern Tiger Swallowtail - Papilio glaucus Gray Hairstreak - Strymon melinus Spicebush Swallowtail - Papilio troilus Red-banded Hairstreak - Calycopis cecrops Palamedes Swallowtail - Papilio palamedes Blues (Subfamily - Polommatinae) Ceraunus Blue - Hemiargus ceraunus Eastern-Tailed Blue - Everes comyntas WHITES AND SULPHURS Spring Azure - Celastrina ladon (Family PIERIDAE) Whites (Subfamily - Pierinae) BRUSHFOOTS Cabbage White - Pieris rapae (Family NYMPHALIDAE) Falcate Orangetip - Anthocharis midea Snouts (Subfamily - Libytheinae) American Snout - Libytheana carinenta Sulphurs and Yellows (Subfamily - Coliadinae) Clouded Sulphur - Colias philodice Heliconians and Fritillaries Orange Sulphur - Colias eurytheme (Subfamily - Heliconiinae) Southern Dogface - Colias cesonia Gulf Fritillary - Agraulis vanillae Cloudless Sulphur - Phoebis sennae Zebra Heliconian - Heliconius charithonia Barred Yellow - Eurema daira Variegated Fritillary -
149 Genus Ypthimomorpha Van
AFROTROPICAL BUTTERFLIES 17th edition (2018). MARK C. WILLIAMS. http://www.lepsocafrica.org/?p=publications&s=atb Genus Ypthimomorpha van Son, 1955 Transvaal Museum Memoirs No. 8: 158 (1-166). Type-species: Ypthima itonia Hewitson, by original designation. The genus Ypthimomorpha belongs to the Family Nymphalidae Rafinesque, 1815; Subfamily Satyrinae Boisduval, 1833; Tribe Satyrini Boisduval, 1833; Subtribe Ypthimina, Reuter, 1896. The other genera in the Subtribe Ypthimina in the Afrotropical Region are Ypthima, Mashuna, Mashunoides, Strabena, Neocoenyra, Coenyropsis, Coenyra, Physcaeneura, Neita, Melampius, Cassionympha, Pseudonympha, Paternympha and Stygionympha. Ypthimomorpha (Marsh Ringlet) is an Afrotropical genus containing a single species. Closely related to the genus Ypthima. Several of the species of Ypthima from Asia have genitalia like those of Ypthimomorpha and more properly belong in this genus (Kielland, 1990d: 86). Emmel & Sourakov propose that Ypthimomorpha should be treated as a subgenus of Ypthima, a view with which Larsen (2005a) does not concur. *Ypthimomorpha itonia (Hewitson, 1865) Marsh Ringlet Ypthima itonia Hewitson, 1865. Transactions of the Entomological Society of London (3) 2: 287 (281-294). Ypthimomorpha itonia (Hewitson, 1865). Van Son, 1955. Ypthimomorpha itonia (Hewitson, 1865). Dickson & Kroon, 1978. Ypthimomorpha itonia (Hewitson, 1865). Pringle et al., 1994: 72. Ypthimomorpha itonia. Male (Wingspan 31 mm). Left – upperside; right – underside. Victoria Falls, Zimbabwe. 17 June 2006. J. Dobson. Images M.C. Williams ex Dobson Collection. 1 Ypthimomorpha itonia. Female. Left – upperside; right – underside. Pungwe, Zimbabwe. 16 April 1995. Images M.C. Williams ex J. Greyling Collection. ?Ypthimomorpha itonia. Male (?wet season form). Left – upperside; right – underside. Dzangha-Ndoki, Congo Republic. J. O’Dell. Images M.C. -
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. -
Diversification of the Cold-Adapted Butterfly Genus Oeneis Related to Holarctic Biogeography and Climatic Niche Shifts
Published in Molecular Phylogenetics and Evolution 92: 255–265, 2015 which should be cited to refer to this work. Diversification of the cold-adapted butterfly genus Oeneis related to Holarctic biogeography and climatic niche shifts q ⇑ I. Kleckova a,b, , M. Cesanek c, Z. Fric a,b, L. Pellissier d,e,f a Faculty of Science, University of South Bohemia, Branišovská 31, 370 05 Cˇeské Budeˇjovice, Czech Republic b Institute of Entomology, Biology Centre of the Czech Academy of Sciences, Branišovská 31, 370 05 Cˇeské Budeˇjovice, Czech Republic c Bodrocká 30, 821 07 Bratislava, Slovakia d University of Fribourg, Department of Biology, Ecology & Evolution, Chemin du Musée 10, 1700 Fribourg, Switzerland e Landscape Ecology, Institute of Terrestrial Ecosystems, ETH Zürich, Zürich, Switzerland f Swiss Federal Research Institute WSL, 8903 Birmensdorf, Switzerland Both geographical and ecological speciation interact during the evolution of a clade, but the relative contribution of these processes is rarely assessed for cold-dwelling biota. Here, we investigate the role of biogeography and the evolution of ecological traits on the diversification of the Holarctic arcto-alpine butterfly genus Oeneis (Lepidoptera: Satyrinae). We reconstructed the molecular phylogeny of the genus based on one mitochondrial (COI) and three nuclear (GAPDH, RpS5, wingless) genes. We inferred the biogeographical scenario and the ancestral state reconstructions of climatic and habitat requirements. Within the genus, we detected five main species groups corresponding to the taxonomic division and further paraphyletic position of Neominois (syn. n.). Next, we transferred O. aktashi from the hora to the polixenes species group on the bases of molecular relationships. We found that the genus originated in the dry grasslands of the mountains of Central Asia and dispersed over the Beringian Land Bridges to North America several times independently. -
An Annotated List of the Lepidoptera of Alberta, Canada
A peer-reviewed open-access journal ZooKeys 38: 1–549 (2010) Annotated list of the Lepidoptera of Alberta, Canada 1 doi: 10.3897/zookeys.38.383 MONOGRAPH www.pensoftonline.net/zookeys Launched to accelerate biodiversity research An annotated list of the Lepidoptera of Alberta, Canada Gregory R. Pohl1, Gary G. Anweiler2, B. Christian Schmidt3, Norbert G. Kondla4 1 Editor-in-chief, co-author of introduction, and author of micromoths portions. Natural Resources Canada, Northern Forestry Centre, 5320 - 122 St., Edmonton, Alberta, Canada T6H 3S5 2 Co-author of macromoths portions. University of Alberta, E.H. Strickland Entomological Museum, Department of Biological Sciences, Edmonton, Alberta, Canada T6G 2E3 3 Co-author of introduction and macromoths portions. Canadian Food Inspection Agency, Canadian National Collection of Insects, Arachnids and Nematodes, K.W. Neatby Bldg., 960 Carling Ave., Ottawa, Ontario, Canada K1A 0C6 4 Author of butterfl ies portions. 242-6220 – 17 Ave. SE, Calgary, Alberta, Canada T2A 0W6 Corresponding authors: Gregory R. Pohl ([email protected]), Gary G. Anweiler ([email protected]), B. Christian Schmidt ([email protected]), Norbert G. Kondla ([email protected]) Academic editor: Donald Lafontaine | Received 11 January 2010 | Accepted 7 February 2010 | Published 5 March 2010 Citation: Pohl GR, Anweiler GG, Schmidt BC, Kondla NG (2010) An annotated list of the Lepidoptera of Alberta, Canada. ZooKeys 38: 1–549. doi: 10.3897/zookeys.38.383 Abstract Th is checklist documents the 2367 Lepidoptera species reported to occur in the province of Alberta, Can- ada, based on examination of the major public insect collections in Alberta and the Canadian National Collection of Insects, Arachnids and Nematodes. -
NYMPHALIDAE: SATYRINAE Jaime Pinzón-C
WEB VERSION MARIPOSAS del Bajo Río Caquetá y Apaporis (Amazonia Colombiana) 1 NYMPHALIDAE: SATYRINAE Jaime Pinzón-C. - - Conservación Internacional Colombia Fotos de J. Pinzón-C. Producido por: T. S. Wachter, R. B. Foster, con el apoyo del Ellen Hyndman Fund y Andrew Mellon Foundation. © Jaime Pinzón-C. [[email protected]] Conservation International – Colombia, Cra 13 # 71-41 Bogotá, Colombia: [http://www.conservation.org.co] © Environmental & Conservation Programs, The Field Museum, Chicago, IL 60605 USA. [[email protected]] [www.fmnh.org/animalguides] Rapid Color Guide # 250 versión 1 02/2009 DORSAL VENTRAL Cithaerias pireta aurorina Cithaerias aff. pyritosa Haetera piera Bia actorion WEB VERSION 2 MARIPOSAS del Bajo Río Caquetá y Apaporis (Amazonia Colombiana) NYMPHALIDAE: SATYRINAE Jaime Pinzón-C. - - Conservación Internacional Colombia Fotos de J. Pinzón-C. Producido por: T. S. Wachter, R. B. Foster, con el apoyo del Ellen Hyndman Fund y Andrew Mellon Foundation. © Jaime Pinzón-C. [[email protected]] Conservation International – Colombia, Cra 13 # 71-41 Bogotá, Colombia: [http://www.conservation.org.co] © Environmental & Conservation Programs, The Field Museum, Chicago, IL 60605 USA. [[email protected]] [www.fmnh.org/animalguides] Rapid Color Guide # 250 versión 1 02/2009 DORSAL VENTRAL Pierella astyoche Pierella hortona Pierella lamia Pierella lena Caeruleuptychia caerulea Chloreuptychia agatha WEB VERSION MARIPOSAS del Bajo Río Caquetá y Apaporis (Amazonia Colombiana) 3 NYMPHALIDAE: SATYRINAE Jaime Pinzón-C. - - Conservación Internacional Colombia Fotos de J. Pinzón-C. Producido por: T. S. Wachter, R. B. Foster, con el apoyo del Ellen Hyndman Fund y Andrew Mellon Foundation. © Jaime Pinzón-C. [[email protected]] Conservation International – Colombia, Cra 13 # 71-41 Bogotá, Colombia: [http://www.conservation.org.co] © Environmental & Conservation Programs, The Field Museum, Chicago, IL 60605 USA. -
Do Butterflies Use “Hearing Aids”? Investigating the Structure and Function of Inflated Wing Veins in Nymphalidae
Do butterflies use “hearing aids”? Investigating the structure and function of inflated wing veins in Nymphalidae by Penghui (Carrie) Sun A thesis submitted to the Faculty of Graduate and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Master of Biology in Biology Carleton University Ottawa, Ontario © 2018 Penghui (Carrie) Sun Abstract Many butterfly species within the subfamily Satyrinae (Nymphalidae) have been informally reported to possess a conspicuous “inflated” or “swollen” subcostal vein on each forewing. However, the function and taxonomic diversity of these structures is unknown. This thesis comprises both experimental and comparative approaches to test hypotheses on the function and evolution of these inflated veins. A laser vibrometry study showed that ears in the common wood nymph, Cercyonis pegala, are tuned to sounds between 1-5 kHz and the inflated subcostal vein enhances sensitivity to these sounds. A comparative study showed that all species with inflated veins possess ears, but not all species with ears possess inflated veins. Further, inflated veins were better developed in smaller butterflies. This thesis provides the first evidence for the function of inflated wing veins in butterflies and supports the hypothesis that they function as aids to low frequency hearing. ii Acknowledgements I thank my supervisor Dr. Jayne Yack for the continued guidance and support, throughout my academic program and in beginning my career, as well as an inspired and newfound appreciation I never knew I could have for insects. I thank my committee members Dr. Jeff Dawson and Dr. Charles-Antoine Darveau for their guidance, advice, and support. I thank Dr. -
Tympanal Ears in Nymphalidae Butterflies: Morphological Diversity and Tests on the Function of Hearing
Tympanal Ears in Nymphalidae Butterflies: Morphological Diversity and Tests on the Function of Hearing by Laura E. Hall A thesis submitted to the Faculty of Graduate Studies and Postdoctoral Affairs in partial fulfillment of the requirements for the degree of Master of Science in Biology Carleton University Ottawa, Ontario, Canada © 2014 Laura E. Hall i Abstract Several Nymphalidae butterflies possess a sensory structure called the Vogel’s organ (VO) that is proposed to function in hearing. However, little is known about the VO’s structure, taxonomic distribution or function. My first research objective was to examine VO morphology and its accessory structures across taxa. Criteria were established to categorize development levels of butterfly VOs and tholi. I observed that enlarged forewing veins are associated with the VOs of several species within two subfamilies of Nymphalidae. Further, I discovered a putative light/temperature-sensitive organ associated with the VOs of several Biblidinae species. The second objective was to test the hypothesis that insect ears function to detect bird flight sounds for predator avoidance. Neurophysiological recordings collected from moth ears show a clear response to flight sounds and chirps from a live bird in the laboratory. Finally, a portable electrophysiology rig was developed to further test this hypothesis in future field studies. ii Acknowledgements First and foremost I would like to thank David Hall who spent endless hours listening to my musings and ramblings regarding butterfly ears, sharing in the joy of my discoveries, and comforting me in times of frustration. Without him, this thesis would not have been possible. I thank Dr. -
Coastal Butterflies & Host Plants
GIANT SKIPPERS Family: Hesperiidae, Subfamily: Megathymi- nae Yucca Giant-Skipper: Megathymus yuccae Host: Yuccas (Yucca aloifolia, Y. gloriosa, Y. fila- mentosa, Y. flaccida) Carolina Satyr S. Pearly-eye Gemmed Satry Viola’s Wood-Satyr Horace’s Duskywing by Gosse Silver-spotted Skipper nectaring on pickerlweed Butterflies need native host plants to complete SATYRS their life cycle. The larvae of many species can Family: Nymphalidae, Subfamily: Satyrinae only survive on specific plants; think of mon- Southern Pearly-eye: Enodia portlandia * archs and milkweeds, longwings and passion- Host: Switchcane (Arundinaria tecta) flowers. The host plants listed here are native to the coastal region of Georgia & South Caro- Creole Pearly Eye: Enodia creola Delaware Skipper Long-tailed Skipper Host: Switchcane (Arundinaria tecta) lina. They provide a critical link for butterfly survival. Protect native plants in your landscape Appalachian Brown: Satyrodes appalachia and grow them in your gardens to support Host: Carex spp., Rhynchospora spp. these important pollinators. Gemmed Satyr: Cyllopsis gemma * Host: Woodoats (Chasmanthium laxum, C. ses- siliflorum) Sachem Skipper Whirlabout Skipper Carolina Satyr: Hermeuptychia sosybius * Host: St. Augustine (Stenotaphrum secundatum) Georgia Satyr: Neonympha areolata Host: Sawgrass (Cladium jamaicense), Sedges (Cyperaceae) Fiery Skipper Checkered Skipper Provided by Coastal WildScapes Little Wood Satyr: Megisto cymela * Twin-spotted Skipper Lace-winged Roadside (www.coastalwildscapes.org) Host: St. Augustine -
Shawnee National Forest
Emperors Subfamily Apaturinae Northern Cloudywing Thorybes pylades Hackberry Emperor Asterocampa celtis Butterflies of the Tawny Emperor Asterocampa clyton Grass-Skippers Subfamily Hesperiinae Shawnee Lace-winged Roadside-skipper Amblyscirtes aesculapius Satyrs Subfamily Satyrinae Bell’s Roadside-skipper Amblyscirtes belli Common Wood-nymph Cercyonis pegala Pepper and Salt Skipper Amblyscirtes hegon National Forest Gemmed Satyr Cyllopsis gemma Linda’s Road-side Skipper Amblyscirtes linda Northern Pearly-eye Enodia anthedon Delaware Skipper Anatrytone logan Least Skipper Ancyloxypha numitor Sachem Atalopedes campestris Dusted Skipper Atrytonopsis hianna Dion Skipper Euphyes dion Dukes’ Skipper Euphyes dukesi Dun Skipper Euphyes vestris Leonard’s Skipper Hesperia leonardus Creole Pearly-eye Enodia creola Cobweb Skipper Hesperia metea Southern Pearly-eye Enodia portlandia Carolina Satyr Hermeuptychia sosybius Fiery Skipper Hylephila phyleus Little Wood-satyr Megisto cymela Swarthy Skipper Nastra Iherminier Appalachian Brown Satyrodes appalachia Hobomok Skipper Poanes hobomok Yehl Skipper Poanes yehl Monarchs Subfamily Danainae Zabulon Skipper Poanes zabulon Monarch Danaus plexippus Crossline Skipper Polites origenes Striped Hairstreak Peck’s Skipper Polites peckius Satyrium liparops Tawny-edged Skipper Polites themistocles Skippers Family Hesperiidae Little Glassywing Pompeius verna Spread-wing Skippers Subfamily Pyrginae Byssus Skipper Problema byssus Achalarus lyciades Hoary Edge Northern Broken-dash Wallengrenia egeremet Golden Banded- -
A SKELETON CHECKLIST of the BUTTERFLIES of the UNITED STATES and CANADA Preparatory to Publication of the Catalogue Jonathan P
A SKELETON CHECKLIST OF THE BUTTERFLIES OF THE UNITED STATES AND CANADA Preparatory to publication of the Catalogue © Jonathan P. Pelham August 2006 Superfamily HESPERIOIDEA Latreille, 1809 Family Hesperiidae Latreille, 1809 Subfamily Eudaminae Mabille, 1877 PHOCIDES Hübner, [1819] = Erycides Hübner, [1819] = Dysenius Scudder, 1872 *1. Phocides pigmalion (Cramer, 1779) = tenuistriga Mabille & Boullet, 1912 a. Phocides pigmalion okeechobee (Worthington, 1881) 2. Phocides belus (Godman and Salvin, 1890) *3. Phocides polybius (Fabricius, 1793) =‡palemon (Cramer, 1777) Homonym = cruentus Hübner, [1819] = palaemonides Röber, 1925 = ab. ‡"gunderi" R. C. Williams & Bell, 1931 a. Phocides polybius lilea (Reakirt, [1867]) = albicilla (Herrich-Schäffer, 1869) = socius (Butler & Druce, 1872) =‡cruentus (Scudder, 1872) Homonym = sanguinea (Scudder, 1872) = imbreus (Plötz, 1879) = spurius (Mabille, 1880) = decolor (Mabille, 1880) = albiciliata Röber, 1925 PROTEIDES Hübner, [1819] = Dicranaspis Mabille, [1879] 4. Proteides mercurius (Fabricius, 1787) a. Proteides mercurius mercurius (Fabricius, 1787) =‡idas (Cramer, 1779) Homonym b. Proteides mercurius sanantonio (Lucas, 1857) EPARGYREUS Hübner, [1819] = Eridamus Burmeister, 1875 5. Epargyreus zestos (Geyer, 1832) a. Epargyreus zestos zestos (Geyer, 1832) = oberon (Worthington, 1881) = arsaces Mabille, 1903 6. Epargyreus clarus (Cramer, 1775) a. Epargyreus clarus clarus (Cramer, 1775) =‡tityrus (Fabricius, 1775) Homonym = argentosus Hayward, 1933 = argenteola (Matsumura, 1940) = ab. ‡"obliteratus" -
A Distinctive New Species of Hermeuptychia Forster, 1964 from the Eastern Tropical Andes (Lepidoptera: Nymphalidae: Satyrinae)
NAKAHARA ET AL.: A new species of Hermeuptychia TROP. LEPID. RES., 26(2): 77-84, 2016 77 A distinctive new species of Hermeuptychia Forster, 1964 from the eastern tropical Andes (Lepidoptera: Nymphalidae: Satyrinae) Shinichi Nakahara1*, Denise Tan1, Gerardo Lamas2, Anamaria Parus1, and Keith R. Willmott1 1. McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, Gainesville, FL 32611, USA 2. Museo de Historia Natural, Universidad Nacional Mayor de San Marcos, Lima, Peru *corresponding author: [email protected] Abstract: A distinctive new species from montane forest in the eastern tropical Andes is described in the taxonomically complex genus Hermeuptychia Forster, 1964. Unusually for the genus, the new species, H. clara Nakahara, Tan, Lamas & Willmott n. sp. is readily distinguished from all other Hermeuptychia on the basis of the ventral wing pattern. A summary of the morphology, biology, distribution and relationships of the species is provided. Key words: Neotropical, Hermeuptychia, Hermeuptychia clara n. sp., Ecuador, Peru, montane forest Resumen: Una nueva especie distintiva del bosque montano del oriente de los Andes tropicales, es descrita para el género taxonómicamente complejo Hermeuptychia Forster, 1964. Inusualmente para el género, la nueva especie, H. clara Nakahara, Tan, Lamas & Willmott n. sp. se distingue fácilmente de todas las otras Hermeuptychia sobre la base del patrón de coloración ventral. Se proporciona un resumen de la morfología, biología, distribución y relaciones de la especie. Palabras clave: Neotropical, Hermeuptychia, Hermeuptychia clara n. sp., Ecuador, Perú, bosque montano INTRODUCTION iceberg, with ongoing molecular study by DT, N. Grishin, N. Seraphim and other collaborators suggesting that the true The Neotropical butterfly genus Hermeuptychia Forster, species diversity of this genus is seriously underestimated (Tan, 1964 is one of the most taxonomically complex genera of unpubl.