DOCSLIB.ORG

Butterflies and Moths of Nayarit, Mexico

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Butterflies and Moths of Nayarit, Mexico Heliothis ononis Flax Bollworm Moth Coptotriche aenea Blackberry Leafminer Argyresthia canadensis Apyrrothrix araxes Dull Firetip Phocides pigmalion Mangrove Skipper Phocides belus Belus Skipper Phocides palemon Guava Skipper Phocides urania Urania skipper Proteides mercurius Mercurial Skipper Epargyreus zestos Zestos Skipper Epargyreus clarus Silver-spotted Skipper Epargyreus spanna Hispaniolan Silverdrop Epargyreus exadeus Broken Silverdrop Polygonus leo Hammock Skipper Polygonus savigny Manuel's Skipper Chioides albofasciatus White-striped Longtail Chioides zilpa Zilpa Longtail Chioides ixion Hispaniolan Longtail Aguna asander Gold-spotted Aguna Aguna claxon Emerald Aguna Aguna metophis Tailed Aguna Typhedanus undulatus Mottled Longtail Typhedanus ampyx Gold-tufted Skipper Polythrix octomaculata Eight-spotted Longtail Polythrix mexicanus Mexican Longtail Polythrix asine Asine Longtail Polythrix caunus (Herrich-Schäffer, 1869) Zestusa dorus Short-tailed Skipper Codatractus carlos Carlos' Mottled-Skipper Codatractus alcaeus White-crescent Longtail Codatractus yucatanus Yucatan Mottled-Skipper Codatractus arizonensis Arizona Skipper Codatractus valeriana Valeriana Skipper Urbanus proteus Long-tailed Skipper Urbanus viterboana Bluish Longtail Urbanus belli Double-striped Longtail Urbanus pronus Pronus Longtail Urbanus esmeraldus Esmeralda Longtail Urbanus evona Turquoise Longtail Urbanus dorantes Dorantes Longtail Urbanus teleus Teleus Longtail Urbanus tanna Tanna Longtail Urbanus simplicius Plain Longtail Urbanus procne Brown Longtail Urbanus doryssus White-tailed Longtail Astraptes fulgerator Two-barred Flasher Astraptes egregius Small-spotted Flasher Astraptes alardus Frosted Flasher Astraptes habana Frosty Flasher Astraptes alector Gilbert's Flasher Astraptes anaphus Yellow-tipped Flasher Autochton cellus Golden Banded-Skipper Autochton pseudocellus Sonoran Banded-Skipper Autochton cincta Chisos Banded-Skipper Autochton vectilucis Central American Banded-Skipper Autochton neis Broad Banded-Skipper Autochton longipennis Spike Banded-Skipper Achalarus lyciades Hoary Edge Achalarus casica Desert Cloudywing Achalarus tehuacana Tehuacan or Dark Cloudywing Achalarus albociliatus Skinner's Cloudywing Achalarus toxeus Coyote Cloudywing Thessia jalapus Jalapus Cloudywing Thorybes drusius Drusius Cloudywing Thorybes pylades Northern Cloudywing Thorybes bathyllus Southern Cloudywing Thorybes confusis Confused Cloudywing Thorybes diversus Western Cloudywing Thorybes mexicana Mexican Cloudywing Cabares potrillo Potrillo Skipper Celaenorrhinus fritzgaertneri Fritzgaertner's Flat Celaenorrhinus stallingsi Stallings' Flat Celaenorrhinus stola Slota Flat Spathilepia clonius Falcate Skipper Cogia hippalus Acacia Skipper Cogia outis Outis Skipper Cogia caicus Gold-costa Skipper Cogia calchas Mimosa Skipper Bungalotis quadratum Pallid Scarlet-eye Arteurotia tractipennis Starred Skipper Polyctor cleta Cleta Tufted-Skipper Polyctor enops Enops Tufted-Skipper Nisoniades rubescens Purplish-black Skipper Pellicia arina Glazed Pellicia Pellicia dimidiata Morning Glory Pellicia Noctuana stator Red-studded Skipper Noctuana lactifera Cryptic Skipper Windia windi Wind's Skipper Bolla brennus Obscure Bolla Bolla eusebius Spatulate Sootywing Bolla clytius Mottled Bolla Staphylus ceos Golden-headed Scallopwing Staphylus vulgata Golden-snouted Sootywing Staphylus hayhurstii Hayhurst's Scallopwing Staphylus mazans Mazans Scallopwing Staphylus ascalaphus Central American Sootywing or Mauve Scallopwing Staphylus azteca Aztec Scallopwing Gorgythion begga Variegated Skipper Sostrata nordica Blue-studded Skipper Paches polla Polla Blue-Skipper Carrhenes canescens Hoary Skipper Carrhenes fuscescens Tanned Hoary-Skipper Xenophanes tryxus Glassy-winged Skipper Onenses hyalophora Crystal-winged Skipper Antigonus emorsa White Spurwing Antigonus erosus Antigonus nearchus Large Spurwing Mylon pelopidas Pale Mylon / Dingy Mylon Mylon lassia Bold Mylon Systasea pulverulenta Texas Powdered Skipper Systasea zampa Arizona Powdered Skipper Achlyodes busirus heros Giant Sicklewing Achlyodes pallida Pale Sicklewing Eantis tamenund Northern Sicklewing Eantis papinianus Cuban Sicklewing Zera hyacinthinus Bruised Skipper Quadrus lugubris Tanned Blue-Skipper Atarnes sallei Orange-spotted Skipper Grais stigmaticus Hermit Skipper Timochares ruptifasciata Brown-banded Skipper Timochares trifasciata Many-banded Skipper Anastrus sempiternus Common Anastrus Anastrus neaeris neaeris Brilliant Anastrus Ebrietas anacreon Common Bent-Skipper Helias cama Squared Bent-Skipper Theagenes aegides White-centered Bent-Skipper Chiomara georgina White-patched Skipper Chiomara mithrax Slaty Skipper Gesta invisus False Duskywing Ephyriades zephodes Zephodes Duskywing Ephyriades arcas Caribbean Duskywing Ephyriades brunnea Florida Duskywing Erynnis icelus Dreamy Duskywing Erynnis brizo Sleepy Duskywing Erynnis juvenalis Juvenal's Duskywing Erynnis telemachus Rocky Mountain Duskywing Erynnis propertius Propertius Duskywing Erynnis meridianus Meridian Duskywing Erynnis scudderi Scudder's Duskywing Erynnis horatius Horace's Duskywing Erynnis tristis Mournful Duskywing Erynnis martialis Mottled Duskywing Erynnis pacuvius Pacuvius Duskywing Erynnis zarucco Zarucco Duskywing Erynnis funeralis Funereal Duskywing Erynnis baptisiae Wild Indigo Duskywing Erynnis lucilius Columbine Duskywing Erynnis afranius Afranius Duskywing Erynnis persius Persius Duskywing Aethilla lavochrea Yellow-rimmed Skipper Aethilla echina Echina Skipper Anisochoria bacchus Northern Snout-Skipper Pyrgus centaureae Grizzled Skipper Pyrgus ruralis Two-banded Checkered-Skipper Pyrgus xanthus Mountain Checkered-Skipper Pyrgus scriptura Small Checkered-Skipper Pyrgus communis Common Checkered-Skipper Pyrgus albescens White Checkered-Skipper Pyrgus adepta Central American Checkered-Skipper Pyrgus philetas Desert Checkered-Skipper Pyrgus oileus Tropical Checkered-Skipper Pyrgus crisia Antillean Checkered-Skipper Heliopyrgus domicella Erichson's White-Skipper Heliopyrgus sublinea Heliopetes ericetorum Northern White-Skipper Heliopetes macaira Turk's-cap White-Skipper Heliopetes laviana Laviana White-Skipper Heliopetes arsalte Veined White-Skipper Heliopetes alana Alana White-Skipper Celotes nessus Common Streaky-Skipper Celotes limpia Scarce Streaky-Skipper Pholisora catullus Common Sootywing Pholisora mejicanus Mexican Sootywing Hesperopsis libya Mohave Sootywing Hesperopsis alpheus Saltbush Sootywing Hesperopsis gracielae MacNeill's Sootywing Creonpyge creon Creon Skipper Carterocephalus palaemon Arctic Skipper Piruna pirus Russet Skipperling Piruna haferniki Chisos Skipperling Piruna polingii Four-spotted Skipperling Piruna aea Many-spotted Skipperling Piruna microstictus Small-spotted Skipperling Piruna penaea Hour-glass Skipperling Synapte malitiosa Malicious Skipper Synapte pecta Northern Faceted-Skipper Synapte syraces Bold Faceted Skipper Synapte shiva Faded Faceted Skipper Synapte salenus Salenus Skipper Anthoptus epictetus Trailside Skipper Corticea corticea Redundant Skipper Zariaspes mys Mys Skipper Vinius tryhana Gold-washed Skipper Apaustus gracilis Delicate Skipper Callimormus saturnus Saturnus Skipper Mnasicles geta Violet-frosted Skipper Vidius perigenes Pale-rayed Skipper Monca crispinus Violet-patched Skipper Nastra lherminier Swarthy Skipper Nastra neamathla Neamathla Skipper Nastra julia Julia's Skipper Cymaenes tripunctus Three-spotted Skipper Cymaenes alumna Alumna Skipper Cymaenes trebius Fawn-spotted Skipper Vehilius inca Inca Skipper Vehilius stictomenes Pasture Skipper Lerema accius Clouded Skipper Lerema ancillaris Liris Skipper Niconiades nikko Nikko Skipper Vettius fantasos Fantastic Skipper Joanna joanna Joanna's Skipper Perichares philetes Green-backed Ruby-eye Rhinthon osca Osca Skipper Rhinthon bushi Bush's Skipper Decinea percosius Double-dotted Skipper Decinea decinea Huastecan Skipper Orthos lycortas Lycortas Skipper Conga chydaea Hidden-ray Skipper Ancyloxypha numitor Least Skipper Ancyloxypha arene Tropical Least Skipper Oarisma garita Garita Skipperling Oarisma poweshiek Poweshiek Skipperling Oarisma edwardsii Edwards' Skipperling Copaeodes aurantiaca Orange Skipperling Copaeodes minima Southern Skipperling Adopaeoides prittwitzi Sunrise Skipper Thymelicus lineola European Skipper Hylephila phyleus Fiery Skipper Pseudocopaeodes eunus Alkali Skipper Stinga morrisoni Morrison's Skipper Hesperia uncas Uncas Skipper Hesperia juba Juba Skipper Hesperia comma Common Branded Skipper Hesperia assiniboia Plains Skipper Hesperia colorado Western Branded Skipper Hesperia woodgatei Apache Skipper Hesperia ottoe Ottoe Skipper Hesperia leonardus Leonard's Skipper Hesperia pahaska Pahaska Skipper Hesperia columbia Columbian Skipper Hesperia metea Cobweb Skipper Hesperia viridis Green Skipper Hesperia attalus Dotted Skipper Hesperia meskei Meske's Skipper Hesperia dacotae Dakota Skipper Hesperia lindseyi Lindsey's Skipper Hesperia sassacus Indian Skipper Hesperia miriamae Sierra Skipper Hesperia nevada Nevada Skipper Atalopedes campestris Sachem Atalopedes mesogramma Mesogramma Skipper Polites rhesus Rhesus Skipper Polites carus Carus Skipper Polites peckius Peck's Skipper Polites sabuleti Sandhill Skipper Polites draco Draco Skipper Polites mardon Mardon Skipper Polites themistocles Tawny-edged Skipper Polites baracoa Baracoa Skipper Polites origenes Crossline Skipper Polites mystic Long Dash Polites sonora Sonora Skipper Polites vibex Whirlabout Wallengrenia egeremet Northern Broken-Dash Wallengrenia otho Southern
Load more

Recommended publications
  • Part B: for Private and Commercial Use
    RESTRICTED ANIMAL LIST (PART B) §4-71-6.5 PART B: FOR PRIVATE AND COMMERCIAL USE SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Haplotaxida FAMILY Lumbricidae Lumbricus rubellus earthworm, red PHYLUM Arthropoda CLASS Crustacea ORDER Amphipoda FAMILY Gammaridae Gammarus (all species in genus) crustacean, freshwater; scud FAMILY Hyalellidae Hyalella azteca shrimps, imps (amphipod) ORDER Cladocera FAMILY Sididae Diaphanosoma (all species in genus) flea, water ORDER Cyclopoida FAMILY Cyclopidae Cyclops (all species in genus) copepod, freshwater ORDER Decapoda FAMILY Alpheidae Alpheus brevicristatus shrimp, Japan (pistol) FAMILY Palinuridae Panulirus gracilis lobster, green spiny Panulirus (all species in genus lobster, spiny except Panulirus argus, P. longipes femoristriga, P. pencillatus) FAMILY Pandalidae Pandalus platyceros shrimp, giant (prawn) FAMILY Penaeidae Penaeus indicus shrimp, penaeid 49 RESTRICTED ANIMAL LIST (Part B) §4-71-6.5 SCIENTIFIC NAME COMMON NAME Penaeus californiensis shrimp, penaeid Penaeus japonicus shrimp, wheel (ginger) Penaeus monodon shrimp, jumbo tiger Penaeus orientalis (chinensis) shrimp, penaeid Penaeus plebjius shrimp, penaeid Penaeus schmitti shrimp, penaeid Penaeus semisulcatus shrimp, penaeid Penaeus setiferus shrimp, white Penaeus stylirostris shrimp, penaeid Penaeus vannamei shrimp, penaeid ORDER Isopoda FAMILY Asellidae Asellus (all species in genus) crustacean, freshwater ORDER Podocopina FAMILY Cyprididae Cypris (all species in genus) ostracod, freshwater CLASS Insecta
    [Show full text]
  • Book Reviews, New Publica- Tions, Metamorphosis, Announcements
    ________________________________________________________________________________________ Volume 57, Number 4 Winter 2015 www.lepsoc.org ________________________________________________________________________________________ Inside: Butterflies of Bolivia Are there caterpillars on butterfly wings? A citizen science call for action Ghost moths of the world website A conservation concern from the 1870’s Fruit-feeding Nymphali- dae in a west Mexican neotropical garden Fender’s Blue Butterfly conservation and re- covery Membership Updates, Marketplace, Book Reviews, New Publica- tions, Metamorphosis, Announcements ... ... and more! ________________________________________________________________________________________ ________________________________________________________ Contents ________________________________________________________www.lepsoc.org Species diversity and temporal distribution in a community of fruit- ____________________________________ feeding Nymphalidae in a west Mexican neotropical garden Volume 57, Number 4 Gerald E. Einem and William Adkins. ............................................... 163 Winter 2015 Windows for butterfly nets The Lepidopterists’ Society is a non-profit ed- J. Alan Wagar. ................................................................................... 173 ucational and scientific organization. The ob- Announcements: .......................................................................................... 174 ject of the Society, which was formed in May Zone Coordinator Needed; Season Summary
    [Show full text]
  • Interações Evolutivas Entre Borboletas Da Tribo Troidini (Papilionidae
    Universidade Estadual de Campinas Instituto de Biologia Interações evolutivas entre borboletas da tribo Troidini (Papilionidae, Papilioninae) e suas plantas hospedeiras no gênero Aristolochia (Aristolochiaceae) Karina Lucas da Silva-Brandão Tese apresentada ao Instituto de Biologia da Universidade Estadual de Campinas para obtenção do título de Doutor em Ecologia Orientadora: Profa. Dra. Vera Nisaka Solferini (IB, Depto de Genética e Evolução) Co-orientador: Prof. Dr. José Roberto Trigo (IB, Depto. de Zoologia) Campinas, abril de 2005 i FICHA CATALOGRÁFICA ELABORADA PELA BIBLIOTECA DO INSTITUTO DE BIOLOGIA - UNICAMP Silva-Brandão, Karina Lucas da Si38li Interações evolutivas entre borboletas da tribo Troidini (Papilionidae, Papilioninae) e suas plantas hospedeiras no gênero Aristolochia (Aristolochiaceae) / Karina Lucas da Silva-Brandão. -- Campinas, SP: [s.n.], 2005. Orientadora: Vera Nisaka Solferini. Co-orientador: José Roberto Trigo. Tese (Doutorado) - Universidade Estadual de Campinas. Instituto de Biologia. 1. Aristolochia. 2. Troidini. 3. Interação inseto-planta. 4. Filogenia molecular. 5. Uso de hospedeiros. I. Vera Nisaka Solferini. 11. José Roberto Trigo. lU. Universidade Estadual de Campinas. Instituto de Biologia. IV. Título. ii iii iv Ilustração: Dadí ([email protected]) “The scientist does not study nature because it is useful to do so. He studies it because he takes pleasure in it; and he takes pleasure in it because it is beautiful. If nature were not beautiful, it would not be worth knowing and life would not be worth living”. Henri Poincaré, The value of Science v vi Agradecimentos Esta tese não teria existido sem a ajuda de muitos amigos e profissionais que deram sua contribuição ao longo desses quatro anos de trabalho.
    [Show full text]
  • Insecta: Lepidoptera)
    Papilionoidea de la Sierra de Huautla, Morelos y Puebla, México (Insecta: Lepidoptera) Mercedes Luna-Reyes1, Jorge Llorente-Bousquets2* & Armando Luis-Martínez2 1. Museo de Zoología, Facultad de Estudios Superiores Zaragoza, Av. Guelatao No. 66. Col. Ejército de Oriente. Iztapalapa. México D.F. 09230; [email protected], [email protected] 2. Museo de Zoología, Facultad de Ciencias, UNAM. Apartado Postal 70-399, México D.F. 04510. *Responsable de la publicación; jlb@ hp.fciencias.unam.mx Recibido 04-VIII-2007. Corregido 30-VI-2008. Aceptado 31-VII-2008. Abstract: Papilionoidea from Sierra de Huautla, Morelos and Puebla, México (Insecta: Lepidoptera). The Cuenca del Balsas region has significant biodiversity and endemicity of its herpetofauna, avifauna and vascular plants. Despite this, our knowledge of the Papilionoidea of the region is poor. We analyzed the local and temporal distribution of Papilionoidea at 24 localities in the states of Morelos and Puebla. The study sites are situated between 900 and 1300 m. a. s. l., and are composed of dry tropical forest (dtf). We recorded 8790 individuals of 83 genera and 142 species of Papilionoidea (sensu Kristensen, 1975), over 79 days of field work, with 2-4 days at each of the 24 localities. Twenty five species were newly recorded for the state of Puebla. Our data render Morelos and Puebla among the seven richest Mexican states, in terms of Papilionoidea diversity. Our results show that the Sierra de Huautla has the lowest diversity, but the highest standard abundance, compared to other Mexican regions with similar vegetation. Patterns of diversity and seasonal abundance are atypical, in that individuals of many species are unusually abundant during the wet months.
    [Show full text]
  • FILOGENIA DE LOS TAXONES DEL SUBGÉNERO Parides (LEPIDOPTERA: PAPILIONIDAE) PRESENTES EN COLOMBIA, BASADA EN SECUENCIAS DEL GEN MITOCONDRIAL CITOCROMO OXIDASA I
    FILOGENIA DE LOS TAXONES DEL SUBGÉNERO Parides (LEPIDOPTERA: PAPILIONIDAE) PRESENTES EN COLOMBIA, BASADA EN SECUENCIAS DEL GEN MITOCONDRIAL CITOCROMO OXIDASA I INGRID MARCELA GUTIÉRREZ ROJAS PONTIFICIA UNIVERSIDAD JAVERIANA FACULTAD DE CIENCIAS CARRERA DE BIOLOGÍA BOGOTÁ D.C., 11 DE JULIO DE 2007 FILOGENIA DE LOS TAXONES DEL SUBGÉNERO Parides (LEPIDOPTERA: PAPILIONIDAE) PRESENTES EN COLOMBIA, BASADA EN SECUENCIAS DEL GEN MITOCONDRIAL CITOCROMO OXIDASA I INGRID MARCELA GUTIÉRREZ ROJAS TRABAJO DE GRADO Presentado como requisito parcial para optar al título de: BIOLOGA GIOVANNY FAGUA M.Sc. DIRECTOR PONTIFICIA UNIVERSIDAD JAVERIANA FACULTAD DE CIENCIAS CARRERA DE BIOLOGÍA BOGOTÁ D.C., 11 DE JULIO DE 2007 NOTA DE ADVERTENCIA Artículo 23 de la Resolución No. 13 de Julio de 1946 “La Universidad no se hace responsable por los conceptos emitidos por sus alumnos en sus trabajos de tesis. Sólo velará porque no se publique nada contrario al dogma y a la moral católica y porque las tesis no contengan ataques personales contra persona alguna, antes bien se vea en ellas el anhelo de buscar la verdad y la justicia”. Artículo 23 de la Resolución N° 13 de Julio de 1946. FILOGENIA DE LOS TAXONES DEL SUBGÉNERO Parides (LEPIDOPTERA: PAPILIONIDAE) PRESENTES EN COLOMBIA, BASADA EN SECUENCIAS DEL GEN MITOCONDRIAL CITOCROMO OXIDASA I INGRID MARCELA GUTIÉRREZ ROJAS APROBADO _______________________________________ GIOVANNY FAGUA GONZALEZ, M.Sc. Director ____________________________ ____________________________ MANUEL RUIZ, Ph.D. ANDRES ACOSTA, M.Sc. Jurado Jurado FILOGENIA DE LOS TAXONES DEL SUBGÉNERO Parides (LEPIDOPTERA: PAPILIONIDAE) PRESENTES EN COLOMBIA, BASADA EN SECUENCIAS DEL GEN MITOCONDRIAL CITOCROMO OXIDASA I INGRID MARCELA GUTIÉRREZ ROJAS APROBADO __________________________________ _____________________________ Dra.
    [Show full text]
  • Estudio Comparativo De Bosques Secundarios De Coníferas De La Reserva De Biosfera Sierra De Las Minas, Guatemala: Con Énfasis En Impactos De Manejo Forestal”
    PROGRAMA DE ENSEÑANZA PARA EL DESARROLLO Y LA CONSERVACIÓN ESCUELA DE POSTGRADO “Estudio comparativo de bosques secundarios de coníferas de la Reserva de Biosfera Sierra de las Minas, Guatemala: con énfasis en impactos de manejo forestal” Tesis sometida a consideración de la Escuela de Posgrado, Programa de Educación para el Desarrollo y la Conservación del Centro Agronómico Tropical de Investigación y Enseñanza como requisito para optar por el grado de: Magister Scientiae en Manejo y Conservación de Bosques Tropicales y Biodiversidad Por Lorena Ninel Estrada Chinchilla Turrialba, Costa Rica, 2005 ii DEDICATORIA A mis padres, Héctor Adolfo Estrada Franco y Clara Chinchilla de Estrada. A mis abuelos: Lisandro Antonio Estrada Conde, María Teresa Franco de Estrada, Rita Soto de Chinchilla y Enrique Chinchilla (). A mi hermana Tani. A mi hermano Héctor y su esposa, Alicia. Muy especialmente a mi sobrina Paula. A mis tíos, tías, primos y primas, especialmente a mi prima Nandi, por mantenerme informada sobre la familia. A mis amigos en Guate, que me mantuvieron al tanto de lo que estaba pasando, y me ayudaron a llevar a cabo este trabajo en una u otra forma, especialmente a Silvia, Marlenne, Ana Lucía, Arturo y Mari, Norma y Evelyn. A mis amigos en CATIE: Rosario, Sandrita, Irma, Matt, Rafi, Karim, Jimmy, Fabricio, Ruth, Mariu, Marce, Inty, Nina, Elena, Patty, Maricela, Karla, Jackie y Joel. Los voy a extrañar. A mis paisanos y amigos: Anabella, Titi y Mario, Magaly y Boris, Julio, Paco y Aldo. A la familia Monterroso Barrientos: Erika, Ottoniel, Danielito y Nati por su compañía y apoyo.
    [Show full text]
  • Behaviour and Natural History of Greta Oto in Captivity (Lepidoptera: Nymphalidae: Ithomiinae)
    Vol. 7 No. 2 1996 HALL: Greta oto Natural History 161 TROPICAL LEPIDOPTERA, 7(2): 161-165 BEHAVIOUR AND NATURAL HISTORY OF GRETA OTO IN CAPTIVITY (LEPIDOPTERA: NYMPHALIDAE: ITHOMIINAE) STEPHEN K. HALL 15 Chatsworth Crescent, Allestree, Derby, DE22 2AP, England ABSTRACT.- The life cycle of Greta oto (Hewitson) (Nymphalidae: Ithomiinae) and the suitability of various foodplants are described. Its behaviour in captiviy is discussed. The ability of this species and other butterflies to display apparently natural behaviour and breed in a small greenhouse emphasises the value of captive populations for behavioural research as well as for public exhibition. KEY WORDS: Apocynaceae, breeding, Buddlejaceae, butterfly house, captivity, Central America, Coccidae, Compositae, courtship, egg, Homoptera, immature stages, larva, Neotropical, oviposition, Papilionidae, pupa, pyrrolizidine alkaloids, Rubiaceae, Solanaceae, Verbenaceae. Since the early 1980's, butterfly houses have become very two 5ft (1.5m) flourescent lights, situated near the apex. The greenhouse popular, and have been a source of interest for lepidopterists contains many butterfly nectar sources and larval foodplants of species worldwide. A butterfly house is a simple and ingenious idea, other than those used by G. oto. The observations took place over a three consisting of a glasshouse planted with various flowering plants month period, from November to January. The temperature in the for adult butterflies and various larval foodplants so that the greenhouse varied from a minimum of 4.4°C (40°F) at night to a maximum of 30°C (86°F) during the day; the temperature outside went butterflies can breed in a controlled enviroment. There are two to minimum -5°C (23°F) to a maximum 11 °C (52°F).
    [Show full text]
  • E-Acta Naturalia Pannonica 11 (2016) Redigit Fazekas Imre
    Bálint Zsolt A nappali lepkék magyar nevei The Hungarian Names of Butterflies e-Acta Naturalia Pannonica 11 (2016) Redigit Fazekas Imre Regiograf Intézet | Regiograf Institute Pécs, Hungary 2016 e-Acta Naturalia Pannonica 11: 1–124. | 11.04.2016 | A folyóirat évente 1–3 kötetben zoológiai, botanikai, állatföldrajzi, természetvédelmi és ökológiai tanulmányokat közöl. Ezenkívül helyet biztosít geológiai, paleontológiai és ar- cheológiai írásoknak, rövid közleményeknek, híreknek, könyvismertetőknek. Az archivált publikációk az Országos Széchenyi Könyvtár Elektronikus Periodika Adatbázis és Archí- vumban (EPA) érhetők el: http://epa.oszk.hu/e‐Acta_Naturalia_Pannonica A nyomtatott kötetek a szerkesztő címén rendelhetők meg. The serial is devoted to the study of Hungarian natural sciences and is instrumental in de- fining the key issues contributing to the science and practice of conserving biological di- versity. The journal covers all aspects of systematic and conservation biology. E‐Acta Naturalia Pannonica may be obtained from the Editor on a basis of exchange or via pur- chase. Archives: http://epa.oszk.hu/e‐Acta_Naturalia_Pannonica Szerkesztő | Editor FAZEKAS IMRE E‐mail: [email protected] | [email protected] Szerkesztőbizottság | Editorial Board Bálint Zsolt (H-Budapest) Buschmann Ferenc (H-Jászberény) Pastorális Gábor (SK-Komárno) Szeőke Kálmán (H-Székesfehérvár) Kiadó|Publisher: Regiograf Intézet |Regiograf Institute |Pécs, Hungary Kiadványterv, tördelés, tipográfia |Design, lay-out, typography: Fazekas Imre Nyomtatás |Print: ROTARI Nyomdaipari Kft., Komló http://www.actapannonica.gportal.hu http://epa.oszk.hu/e‐Acta_Naturalia_Pannonica Megjelent |Published: 2016.04.11. |11.04.2016 Minden jog fenntartva | All rights reserved © Regiograf Intézet |Regiograf Institute |Hungary, 2016 HU ISSN 2061–3911 A nappali lepkék magyar nevei The Hungarian Names of Butterflies Bálint Zsolt Abstract: The paper starts with an overview of how vernacular Hungarian names for butterflies were developed or invented.
    [Show full text]
  • A Cladistic Analysis of the Genus Parides Hübner, [1819], Based on Androconial Structures (Lepidoptera: Papilionidae) 119-131 — 119 —
    ZOBODAT - www.zobodat.at Zoologisch-Botanische Datenbank/Zoological-Botanical Database Digitale Literatur/Digital Literature Zeitschrift/Journal: Neue Entomologische Nachrichten Jahr/Year: 1998 Band/Volume: 41 Autor(en)/Author(s): Racheli Tommaso, Olmisania Luca Artikel/Article: A Cladistic Analysis of the genus Parides Hübner, [1819], based on androconial structures (Lepidoptera: Papilionidae) 119-131 — 119 — A Cladistic Analysis of the genusParides H ü b n e r , [1819], based on androconial structures (Lepidoptera: Papilionidae) by Tommaso Racheli & L uca Olmisani Abstract The neotropical species of the genus Parides have been revised through cladistic numerical tech­ nique. The androconial structures of each species were used as the main characters for the analysis. The ingroup Parides comprises four main clades, which are discussed in the light of evolutionary and biogeographic evidence. 1. Introduction The genus Parides Hubner , [1819], has been studied for a long time, but only recently has it been subjected to cladistic analysis. This showed an unresolved monophylum within the Troidini, encom­ passing terminal taxa with South American and Oriental distributions. Miller (1987) hypothesized the monophyly of Parides sensu lato by the following apomorphic characters: 1 - Females with a highly sclerotized invagination dorsally to ductus bursae. 2 - A wide ductus bursae. 3 - A large vesica. While the neotropical subgenus Parides was characterised by: 1 - Dorso-ventrally oriented signa. 2 - Lower level androconia curled. Several approaches aimed to the recognition of relation­ ships among the species groups resulted in different arrangements (Rothschild & J ordan , 1906; Munroe, 1961; Hancock , 1978; Miller 1987; Tyler etal. 1994; Brown et al. 1995). All the species considered are endemic to Central and South America, the larvae are monophagous on Aristolochia plants (Aristolochiaceae), and the adults are linked to mimicry rings (tab.
    [Show full text]
  • Part B: for Private and Commercial Use
    RESTRICTED ANIMAL LIST (PART B) §4-71-6.5 PART B: FOR PRIVATE AND COMMERCIAL USE SCIENTIFIC NAME COMMON NAME INVERTEBRATES PHYLUM Annelida CLASS Oligochaeta ORDER Haplotaxida FAMILY Lumbricidae Lumbricus rubellus earthworm, red PHYLUM Arthropoda CLASS Crustacea ORDER Amphipoda FAMILY Gammaridae Gammarus (all species in genus) crustacean, freshwater; scud FAMILY Hyalellidae Hyalella azteca shrimps, imps (amphipod) ORDER Cladocera FAMILY Sididae Diaphanosoma (all species in genus) flea, water ORDER Cyclopoida FAMILY Cyclopidae Cyclops (all species in genus) copepod, freshwater ORDER Decapoda FAMILY Alpheidae Alpheus brevicristatus shrimp, Japan (pistol) FAMILY Palinuridae Panulirus gracilis lobster, green spiny Panulirus (all species in genus lobster, spiny except Panulirus argus, P. longipes femoristriga, P. pencillatus) FAMILY Pandalidae Pandalus platyceros shrimp, giant (prawn) FAMILY Penaeidae Penaeus indicus shrimp, penaeid Penaeus californiensis shrimp, penaeid 43 RESTRICTED ANIMAL LIST (PART B) §4-71-6.5 SCIENTIFIC NAME COMMON NAME Penaeus japonicus shrimp, wheel (ginger) Penaeus monodon shrimp, jumbo tiger Penaeus orientalis (chinensis) shrimp, penaeid Penaeus plebjius shrimp, penaeid Penaeus schmitti shrimp, penaeid Penaeus semisulcatus shrimp, penaeid Penaeus setiferus shrimp, white Penaeus stylirostris shrimp, penaeid Penaeus vannamei shrimp, penaeid ORDER Isopoda FAMILY Asellidae Asellus (all species in genus) crustacean, freshwater ORDER Podocopina FAMILY Cyprididae Cypris (all species in genus) ostracod, freshwater CLASS Insecta
    [Show full text]
  • Copyright by Krushnamegh Jagannath Kunte 2008
    Copyright by Krushnamegh Jagannath Kunte 2008 The Dissertation Committee for Krushnamegh Jagannath Kunte certifies that this is the approved version of the following dissertation: Evolution of sex-limited mimicry in swallowtail butterflies Committee: _____________________________ Lawrence E. Gilbert, Supervisor _____________________________ Thomas Juenger, Co-supervisor _____________________________ Michael Singer ____________________________ Mark Kirkpatrick _____________________________ Alan Lloyd _____________________________ Peter Andolfatto Evolution of sex-limited mimicry in swallowtail butterflies by Krushnamegh Jagannath Kunte, M.Sc. Dissertation Presented to the Faculty of the Graduate School of The University of Texas at Austin in Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy The University of Texas at Austin December, 2008 Dedication To Alfred Russel Wallace – naturalist extraordinaire – on the 150th anniversary of his discovery of natural selection, in admiration of his work on Indo-Malayan swallowtail butterflies. Acknowledgements More than ever before in my life, this work is a product of years of collaboration with numerous scientists, butterfly collectors and friends. First and foremost, I thank my advisor Lawrence Gilbert who patiently tolerated my academic wanderings for many years, let me find my feet in the academic world, and provided critical guidance, support and inspiration when I needed it most. Thomas Juenger provided lab facilities, some research funding and a lot of advice about lab work. I give special thanks to Michael Singer for varied academic as well as interesting non- academic discussions. My other committee members: Alan Lloyd, Peter Andolfatto and especially Mark Kirkpatrick, have over the years offered constructive criticism of my ideas and also advice on the way forward. Much wisdom about swallowtail butterflies, mimicry and the molecular methods to study them has trickled down to me from Felix Sperling, Rob Plowes, Harry Pavulaan, David Wright and Tierney Wayne.
    [Show full text]
  • Animals Approved for Zoos in New Zealand As of June 2021
    INFORMATION SHEET Animals approved for zoos in New Zealand as of June 2021 This is an alphabetical list of animals that can be held in zoos* in New Zealand. Approval numbers that begin with “PRE” were approved prior to July 29 1998 and were subsequently transferred to the HSNO Act. Approval numbers that begin with “NOC” are animal species approved under the HSNO Act after that date. Key to this document: * Approvals may only be used by facilities that are open to the public and approved by the Ministry for Primary Industries for the containment of that species unless the approval code is followed by one of the following symbols: † The approved zoo facility is not required to be open to the public. †† The approval may only be used by the Keystone Wildlife Conservancy containment facility (now known as Gibbs Wildlife Conservancy). ††† Species can also be held under facilities approved to the MAF/ERMA New Zealand Containment Facilities for Vertebrate Laboratory Animals. Species Common name Approval code Abatus shackletoni Koehler, 1911 Sea urchin (echinoids) PRE008972 Acinonyx jubatus Schreber, 1775 Cheetah PRE008902 Acondaster hodgonsoni Yellow starfish PRE008974 Acontaster conspicuous Yellow starfish PRE008973 Acrobates pygmaeus Shaw, 1793 feather tailed glider NOC002541† Adamussium colbecki Smith, 1902 Antarctic scallop (mollusc) PRE008975 Aerothyris fragilis Smith, 1907 brachiopod (mollusc) PRE008976 Aerothyris joubini Blochmann, 1906 brachiopod (mollusc) PRE008977 Ailuropoda melanoleuca David, 1869 giant panda NOC100015† Ailurus fulgens
    [Show full text]