Costa Rica Butterflies Costa Rica Has More Butterfly Species (1,200+) Than Birds (900+) Due to Its Warm Climate and Diverse Plant Life

Total Page:16

File Type:pdf, Size:1020Kb

Costa Rica Butterflies Costa Rica Has More Butterfly Species (1,200+) Than Birds (900+) Due to Its Warm Climate and Diverse Plant Life Costa Rica Butterflies Costa Rica has more butterfly species (1,200+) than birds (900+) due to its warm climate and diverse plant life. Below are butterflies seen during trips in 2016 and 2017 photographed by Dennis Deck, Dan van den Broek, Liam O’Brien, Dennis Paulson, Buck Snelson, Georges Kleinbaum, Karen Kearney, and Linda LaPan. Species identification from our photos was based primarily on Butterflies of Mexico and Central America by Glassberg (2007) plus online sources in difficult cases but errors are possible. Swallowtails Montezuma’s Cattleheart Polydamas Swallowtail (Battus polydamas) (Parides montezuma) Giant Swallowtail (Papilio cresphontes) Green-celled Cattleheart Variable Cattleheart (Parides erithalion) (Parides childrenae) Ruby-spotted Swallowtail (Heraclides anchisiades) Whites and Yellows Transandean Cattleheart Pink-spotted Cattleheart (Parides photinus) (Parides iphidamas) Thoas Swallowtail (Papilio thoas) Wedge-spotted Cattleheart (Parides panares) Mexican Dartwhite (Catasticta nimbice) M Green-eyed White (Leptophobia aripa) Large Orange Sulphur (Phoebis agarithe) F Great Southern White (Ascia monuste) Ghost Yellow (Eurema albula) Common Melwhite (Melete lycimnia) Apricot Sulphur (Phoebis argante) Cattleheart White (Archonias brassolis) Golden Melwhite (Melete polyhymnia) Straight-lined Sulphur (Phoebis trite) Cloudless Sulphur (Phoebis sennae) Giant White (Ganyra josephina) Tailed Sulphur (Phoebis neocrypris) White Angled-Sulphur (Anteos clorinde) Statira Sulphur (Aphrissa/Phoebis statira) Hairstreaks Zebra Teaser (Arawacus sepaerata) Dina Yellow (Eurema dina) Skyblue Hairstreak (Pseudolycaena damo) Red-spotted Scrub-Hairstreak (Strymon ziba) Barred Yellow (Eurema daira) Zebra Cross-streak (Panthiades bathildis) Pale Ministreak (Ministrymon una) Scarce Yellow (Eurema xantochlora) Fine-lined Stripe-streak (Arawacus sito) Dusky-blue Groundstreak (Calycopis isobeon) Salome Yellow (Eurema salome) White-rayed Pixie (Melanis cephise) Meton Hairstreak (Rekoa meton) Sword-tailed Beautymark (Rhetus arcius) Red-bordered Pixie (Melanis pixe) Field’s Groundstreak (Calycopis drusilla) Great Jewelmark (Anteros kupris) Orange-barred Pixie (Melanis electron) Goodson’s Greenstreak ? (Cyanophrys goodsoni) Greater Scintillant (Calephelis sixola) Blues Iris Calephelis (Calephelis iris) Ceraunus Blue (Hemiargus ceraunus) Scintillant sp. (Calephelis sp.) Metalmarks Schaus' Calephelis (Calephelis schaus) Metalmark sp. Brushfoots Giant Eyemark (Mesosemia grandis) Cloaked Scintillant (Detritivora barnesi) Gulf Fritillary (Agraulis vanillae) Brilliant Greenmark (Caria mantinea) Mexican Fritillary (Euptoieta hegesia) Sailer’s Lemmark (Thisbe irenea) Greenmark sp. (Caria sp.) Mexican Silverspot (Dione moneta) Variable Lemmark (Synargis mycone) Tanmark sp. (Emesis sp.) Red-spotted Lemmark Juno Heliconian (Dione juno) (Nymphidium onaeum) Blue Metalmark (Lasaia sula) Julia Heliconian (Dryas julia) Blue-winged Sheenmark (Eurybia lycisca) Sara Heliconian (Heliconius sara) Least Heliconian (Euieides aliphera) Zebra Heliconian (Heliconius charithonia) Hewitson’s Heliconian (Heliconius hewitsoni) Lycaste Tigerwing (Hypothyris lycaste) Mexican Helconian (Heliconius hortense) Banded Orange Heliconian (Dryadula phaetusa) Grinning Heliconian (Heliconius cydno) Heart-spotted Heliconian (Heliconius hecale) Nonpassionate Heliconian (Euieides procula) Elf (Microtia elva) Isabella’s Heliconian (Euieides isabella) Five-spotted Heliconian (Heliconius hecalesia) Acting Heliconian (Euieides vibilia) Variable Crescent (Eresia ithomioides) Creamy Crescent (Eresio clio) Theona Checkerspot (Chlosyne theona) Black-bordered Tegosa (Tegosa anieta) Crimson Patch (Chlosyne janais) Pale-banded Crescent (Anthanassa tulcis) Tropical Buckeye (Junonia evarete) Blurry Crescent (Phyciodes nebulosa) Bordered Patch (Chlosyne lacinia) Smudged Crescent (Castilia eranites) White Peacock (Anartia jatrophae) Wide-banded Crescent (Phyciodes tulcis) Three-banded Crescent (Eresia alsina) Pointer Sister (Adelpha iphiclus) Banded Peacock (Anartia fatima) Barnes’ Sister (Adelpha barnesia) Rusty-tipped Page (Siproeta epaphus) Scarce Sister (Adelpha nea) Smooth-banded Sister (Adelpha cytherea) Malachite (Siproeta stelenes) Confusing Sister (Adelpha iphicleola) Yellow-rimmed Eighty-eight (Callicore texa) Green Heliconian (Philaethria dido) --Placed here for comparison-- Band-celled Sister (Adelpha fessonia) Six-spotted Eighty-eight (Callicore lyca) Stitched Sister (Adelpha erotia) Cecropia Sister (Adelpha phylaca) Common Banner (Epiphile adrasta) Stoplight Catone (Catonephele numilia) Guatemalan Cracker (Hamadryas guateamalena) Starry Cracker (Hamadryas laodamia) Orange Banner (Temenis laothoe) Small Beauty (Colobura dirce) Little Banner (Nica flavilla) Gray Cracker (Hamadryas februa) Tiger Beauty (Tigridia acesta) Red Rim (Biblis hyperia) Red Cracker (Hamadryas aphinome) Bloomfield’s Beauty (Smyrna blomfildia) Whitened Bluewing (Myscelia cyaniris) Variable Cracker (Hamadryas feronia) Orange Daggerwing (Marpesia berania) Jazzy Leafwing (Hypna clytemnestra) Dappled Daggerwing (Marpesia merops) Waiter Daggerwing (Marpesia coresia) Tiger Leafwing (Consul fabius) One-spotted Prepona (Archaeoprepona demophon) Godman’s Leafwing (Anaea mora) Many-banded Daggerwing (Marpesia chiron) Two-spotted Prepona (Archaeoprepona demophoon) Orion Cecropian (Historis odius) Angled Leafwing (Anaea glycerium) Ruddy Daggerwing (Marpesia petreus) Tailed Cecopian (Historis acheronta) Hermes Satyr (Hermeuptychia hermes) Almond-eyed Owl-butterfly (Caligo brasiliensis) Pavon Emperor (Doxocopa pavon) Transgressive Saytr (Euptychia jesia) Split-banded Owlet (Opsiphanes cassina) Confused Satyr (Cissia confusa) Quiet Diaph (Pierella luna) White Satyr (Pareuptychia ocirrhoe) Common/Blue Morpho (Morpho helenor) Red-washed Satyr (Pierella helvina) Harmonia Satyr (Hermeuptychia harmonia) Yellow-fronted Owl-butterfly (Caligo telemonius) White-spotted Satyr (Manataria hercyna) Skippers Pink-tipped Satyr (Cithaerias pireta) Disturbed Tigerwing (Mechanitis polymnia) Red-headed Firetip (Pyrrhopyge phidias zenodorus) Guatemalan Ithomia (Ithomia patilla) Confused Tigerwing (Mechanitis lysimnia) Red-collared Firetip (Elbella scylla) Thick-tipped Greta (Greta morgane) Orange-rimmed Firetip (Pyrrhopyge chalybea) Klug’s Dircenna (Dircenna klugii) Monarch (Danaus plexippus) Royal Firetip (Mysoria barcastus ambigua) Heraldica Clearwing (Ithomia heraldica) Tiger Mimic-Queen (Lycorea cleobaea) Blue-lined Firetip (Jemadia patrobas) Mechanitis sp. Guava Skipper (Phocides polybius) Broken Silverdrop (Epargyreus exadeus) Yellow-tipped Skipper (Astraptes anaphus) Beautiful Beamer (Phocides belus) Plain Longtail (Urbanus simplicius) Frosted Flasher (Astraptes alardus) Spineless Silverdrop (Epargyreus aspina) White-edged Longtail (Urbanus albimaro) Gold-spotted Aguna (Aguna asander) White-striped Longtail (Chioides catillus) Silvered Flasher (Astraptes creteus) unknown Aguna (Aguna sp.) Coyote Cloudywing (Achalraus toxeus) White-patched Skipper (Chiomara asychis) Mazans Scallopwing (Staphylus mazans) Golden-snouted Scallopwing Brown Longtail (Urbanus procne) (Staphylus vulgata) Two-barred Flasher (Astraptes fulgerator) Pale Sicklewing (Anchlyodes pallida) Long-tailed Skipper (Urbanus proteus) Short-tailed Flasher (Astraptes brevicauda) Brilliant Blue Skipper (Paches loxus) Sharp Banded-Skipper (Autochton zarex) White-tailed Longtail (Urbanus doryssus) Sharp-banded Skipper (Autochton zarex) Mexican Longtail (Polythrix mexicanus) Bluish Mottled-Skipper (Codatractus imalena) Dark-spotted Polythrix (Polythrix asine) Alana White-Skipper (Heliopetes alana) Sickle-winged Skipper (Achlyodes mithridates) Falcate Skipper (Spathilepia clonius) Five-banded Skipper (Timochares trifasciata) Radiant Brown-Skimmer (Callimormus radiosa) Tropical Checkered-Skipper (Pyrgus oileus) Glassy-winged Skipper (Xenophanes tryxus) Selenus Skipper (Synapte salenus) Erikson’s White-Skipper (Heliopetes domicella) M Pasture Brown-Skipper (Vehilius stictomenes) F? Dusted Spurwing (Antigonus erosus) Veined White-Skipper (Heliopetes arsalte) Latonia Skipper (Cobalopsis latonia) Skipper sp. Mella Skipper (Anatrytone mella) Fantastic Skipper (Vettius fantasos) ? Common Glassywing (Pompeius pompeius) Dun Skipper (Euphyres vestris) Coruscating Skipper (Oxynthes corusca) Green-backed Ruby-eye (Perichares philetes) Common Mellana (Quasimellana eulogius) Brazilian Skipper (Calpodes ethlius) Yellow-spotted Ruby-eye (Telles arcalaus) Eufala Skipper (Lerodea eufala) Whirlabout (Polites vibex) Mimosa Skipper (Cogia calchaes) Olive-clouded Skipper (Lerodea dysaules) (Castniomera drucei) Rich Skipper (Halotus rica) Skipper sp. Day Moths (Isostyla zetila) Sickle-winged Skipper (Eantis tamenund) Predators Glazed Pellicia (Pellicia arina) (Auotmeris postalbida) Praying Mantis eating Gulf Fritillary .
Recommended publications
  • Inside: Idaea Asceta (Prout) (Geometridae), New to the U.S
    ________________________________________________________________________________________ Volume 53, Number 3 Fall 2011 www.lepsoc.org ________________________________________________________________________________________ Inside: Idaea asceta (Prout) (Geometridae), new to the U.S. Lepidoptera conserva- tion under a changing climate Karl Jordan Award win- ner: Don Lafontaine Life history of Leona’s Little Blue Tiputini Biological Sta- tion, Ecuador Late Season trip to the Richardson Mountains Membership Updates, The Mailbag, Marketplace... ... and more! ________________________________________________________________________________________ ________________________________________________________ Contents ________________________________________________________www.lepsoc.org A Late Season Trip to the Richardson Mountains ____________________________________ Michael Leski. ............................................................................................ 75 Volume 53, Number 3 Report on the Southern Lepidoptersists’ Society and Association Fall 2011 for Tropical Lepidoptera Meeting 2011 The Lepidopterists’ Society is a non-profit ed- Jacqueline Y. Miller. ............................................................................. 78 ucational and scientific organization. The ob- Idaea asceta (Prout) (Geometridae: Sterrhinae) from Texas, new ject of the Society, which was formed in May to the North American fauna 1947 and formally constituted in December Charles V. Covell. ...................................................................................
    [Show full text]
  • Lepidoptera Argentina - Parte Vii: Papilionidae
    LEPIDOPTERA ARGENTINA Catálogo ilustrado y comentado de las mariposas de Argentina Parte VII: PAPILIONIDAE Fernando César Penco Osvaldo Di Iorio 2014 PLAN GENERAL DE LA OBRA Parte I CASTNIIDAE Parte II COSSIDAE & LIMACODIDAE Parte III TORTRICIDAE Parte IV SEMATURIDAE & URANIIDAE Parte V GEOMETRIDAE Parte VI HESPERIIDAE Parte VII PAPILIONIDAE Parte VIII PIERIDAE Parte IX LYCAENIDAE Parte X RIODINIDAE Parte XI NYMPHALIDAE & LIBYTHEIDAE Parte XII MEGALOPYGIDAE Parte XIII APATELODIDAE, MIMALLONIDAE & LASIOCAMPIDAE Parte XIV SATURNIIDAE Parte XV SPHINGIDAE Parte XVI EREBIDAE: ARCTIINAE & EREBINAE Parte XVII NOTODONTIDAE Parte XVIII NOCTUIDAE Parte XIX TAXONOMIA DE LEPIDOPTERA Parte XX BIBLIOGRAFIA LEPIDOPTERA ARGENTINA Catálogo ilustrado y comentado de las mariposas de Argentina Parte VII: PAPILIONIDAE Fernando César Penco Osvaldo R. Di Iorio 2014 Copyright © 2014 Fernando César Penco Ninguna parte de esta publicación, incluido el diseño de la portada y de las páginas interiores puede ser reproducida, almacenadas o transmitida de ninguna forma ni por ningún medio, sea éste electrónico, mecánico, grabación, fotocopia o cualquier otro sin la previa autorización escrita del autor. LEPIDOPTERA ARGENTINA - PARTE VII: PAPILIONIDAE Autores: Fernando César Penco Area de Biodiversidad, Fundación de Historia Natural Félix de Azara, Departamento de Ciencias Naturales y Antropológicas CEBBAD, Universidad Maimónides, Ciudad Autónoma de Buenos Aires, Argentina. E-mail: [email protected] Osvaldo R. Di Iorio Entomología, Departamento de Biodiversidad
    [Show full text]
  • MEET the BUTTERFLIES Identify the Butter Ies You've Seen at Butter Ies
    MEET THE BUTTERFLIES Identify the butteries you’ve seen at Butteries LIVE! Learn the scientic, common name and country of origin. Experience the wonderful world of butteries with the help of Butteries LIVE! COMMON MORPHO Morpho peleides Family: Nymphalidae Range: Mexico to Colombia Wingspan: 5-8 in. (12.7 – 20.3 cm.) Fast Fact: Common morphos are attracted to fermenting fruits. WHITE MORPHO Morpho polyphemus Family: Nymphalidae Range: Mexico to Central America Wingspan: 4-4.75 in. (10-12 cm.) Fast Fact: Adult white morphos prefer to feed on rotting fruits or sap from trees. WHITENED BLUEWING Myscelia cyaniris Family: Nymphalidae Range: Mexico, parts of Central and South America Wingspan: 1.3-1.4 in. (3.3-3.6 cm.) Fast Fact: The underside of the whitened bluewing is silvery- gray, allowing it to blend in on bark and branches. MEXICAN BLUEWING Myscelia ethusa Family: Nymphalidae Range: Mexico, Central America, Colombia Wingspan: 2.5-3.0 in. (6.4-7.6 cm.) Fast Fact: Young caterpillars attach dung pellets and silk to a leaf vein to create a resting perch. NEW GUINEA BIRDWING Ornithoptera priamus Family: Papilionidae Range: Australia Wingspan: 5 in. (12.7 cm.) Fast Fact: New Guinea birdwings are sexually dimorphic. Females are much larger than the males, and their wings are black with white markings. LEARN MORE ABOUT SEXUAL DIMORPHISM IN BUTTERFLIES > MOCKER SWALLOWTAIL Papilio dardanus Family: Papilionidae Range: Africa Wingspan: 3.9-4.7 in. (10-12 cm.) Fast Fact: The male mocker swallowtail has a tail, while the female is tailless. LEARN MORE ABOUT SEXUALLY DIMORPHIC BUTTERFLIES > ORCHARD SWALLOWTAIL Papilio demodocus Family: Papilionidae Range: Africa and Arabia Wingspan: 4.5 in.
    [Show full text]
  • English Cop18 Prop. XXX CONVENTION ON
    Original language: English CoP18 Prop. XXX CONVENTION ON INTERNATIONAL TRADE IN ENDANGERED SPECIES OF WILD FAUNA AND FLORA ____________________ Eighteenth meeting of the Conference of the Parties Colombo (Sri Lanka), 23 May – 3 June 2019 CONSIDERATION OF PROPOSALS FOR AMENDMENT OF APPENDICES I AND II A. Proposal: To include the species Parides burchellanus in Appendix I, in accordance with Article II, paragraph 1 of the Convention and satisfying Criteria A i,ii, v; B i,iii, iv and C ii of Resolution Conf. 9.24 (Rev. CoP17). B. Proponent Brazil C. Supporting statement: 1. Taxonomy 1.1 Class: Insecta 1.2 Order: Lepidoptera 1.3 Family: Papilionidae 1.4 Species: Parides burchellanus (Westwood, 1872) 1.5 Synonymies: Papilio jaguarae Foetterle, 1902; Papilio numa Boisduval, 1836; Parides socama Schaus, 1902. 1.6 Common names: English: Swallowtail Portuguese:Borboleta-ribeirinha 2. Overview 1 The present proposal is based on the current knowledge about the species Parides burchellanus, well presented in Volume 7 of the Red Book of the Brazilian Fauna Threatened with Extinction1 and in present data on the supply of specimens for sale in the international market. The species has a restricted distribution2 with populations in the condition of decline as a consequence of anthropic actions in their habitat. It is categorized in Brazil as Critically Endangered (CR), according to criterion C2a(i) of the International Union for Conservation of Nature – IUCN. This criterion implies small and declining populations. In addition, these populations are also hundreds of kilometers apart from each other. The present proposal therefore seeks to reduce the pressure exerted by illegal trade on this species through its inclusion in Annex I to the Convention.
    [Show full text]
  • Phylogenetic Relationships and Historical Biogeography of Tribes and Genera in the Subfamily Nymphalinae (Lepidoptera: Nymphalidae)
    Blackwell Science, LtdOxford, UKBIJBiological Journal of the Linnean Society 0024-4066The Linnean Society of London, 2005? 2005 862 227251 Original Article PHYLOGENY OF NYMPHALINAE N. WAHLBERG ET AL Biological Journal of the Linnean Society, 2005, 86, 227–251. With 5 figures . Phylogenetic relationships and historical biogeography of tribes and genera in the subfamily Nymphalinae (Lepidoptera: Nymphalidae) NIKLAS WAHLBERG1*, ANDREW V. Z. BROWER2 and SÖREN NYLIN1 1Department of Zoology, Stockholm University, S-106 91 Stockholm, Sweden 2Department of Zoology, Oregon State University, Corvallis, Oregon 97331–2907, USA Received 10 January 2004; accepted for publication 12 November 2004 We infer for the first time the phylogenetic relationships of genera and tribes in the ecologically and evolutionarily well-studied subfamily Nymphalinae using DNA sequence data from three genes: 1450 bp of cytochrome oxidase subunit I (COI) (in the mitochondrial genome), 1077 bp of elongation factor 1-alpha (EF1-a) and 400–403 bp of wing- less (both in the nuclear genome). We explore the influence of each gene region on the support given to each node of the most parsimonious tree derived from a combined analysis of all three genes using Partitioned Bremer Support. We also explore the influence of assuming equal weights for all characters in the combined analysis by investigating the stability of clades to different transition/transversion weighting schemes. We find many strongly supported and stable clades in the Nymphalinae. We are also able to identify ‘rogue’
    [Show full text]
  • Reading the Complex Skipper Butterfly Fauna of One Tropical Place
    Reading the Complex Skipper Butterfly Fauna of One Tropical Place Daniel H. Janzen1*, Winnie Hallwachs1, John M. Burns2, Mehrdad Hajibabaei3, Claudia Bertrand3, Paul D. N. Hebert3 1 Department of Biology, University of Pennsylvania, Philadelphia, Pennsylvania, United States of America, 2 Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, D.C., United States of America, 3 Department of Integrative Biology, Biodiversity Institute of Ontario, University of Guelph, Guelph, Canada Abstract Background: An intense, 30-year, ongoing biodiversity inventory of Lepidoptera, together with their food plants and parasitoids, is centered on the rearing of wild-caught caterpillars in the 120,000 terrestrial hectares of dry, rain, and cloud forest of Area de Conservacion Guanacaste (ACG) in northwestern Costa Rica. Since 2003, DNA barcoding of all species has aided their identification and discovery. We summarize the process and results for a large set of the species of two speciose subfamilies of ACG skipper butterflies (Hesperiidae) and emphasize the effectiveness of barcoding these species (which are often difficult and time-consuming to identify). Methodology/Principal Findings: Adults are DNA barcoded by the Biodiversity Institute of Ontario, Guelph, Canada; and they are identified by correlating the resulting COI barcode information with more traditional information such as food plant, facies, genitalia, microlocation within ACG, caterpillar traits, etc. This process has found about 303 morphologically defined species of eudamine and pyrgine Hesperiidae breeding in ACG (about 25% of the ACG butterfly fauna) and another 44 units indicated by distinct barcodes (n = 9,094), which may be additional species and therefore may represent as much as a 13% increase.
    [Show full text]
  • Plantas Alimenticias De 19 Especies De Mariposas Diurnas (Lepidoptera) En Loreto, Perú
    Revista peruana de biología 24(1): 035 - 042 (2017) Plantas alimenticias de 19 especies de mariposasISSN-L 1561-0837 diurnas doi: http://dx.doi.org/10.15381/rpb.v24i1.13109 Facultad de Ciencias Biológicas UNMSM TRABAJOS ORIGINALES Plantas alimenticias de 19 especies de mariposas diurnas (Lepidoptera) en Loreto, Perú Food Plants of 19 butterflies species (Lepidoptera) from Loreto, Peru Joel Vásquez Bardales *1,2, Ricardo Zárate Gómez 1,3, Percy Huiñapi Canaquiri 1,2, Julio Pinedo Jiménez 4, Juan José Ramírez Hernández 5, Gerardo Lamas 5, Pedro Vela García 1,2 1 Instituto de Investigaciones de la Amazonía Peruana (IIAP). Av. A. Quiñones km 2.5, Iquitos, Loreto, Perú 2 Programa de Investigación en Biodiversidad Amazónica (PIBA). 3 Programa de Investigación en Cambio Climático, Desarrollo Territorial y Ambiente (PROTERRA). 4 Universidad Nacional de la Amazonia Peruana, Facultad de Agronomía. Calle Pevas s/n, Iquitos Perú 5 Universidad Nacional Mayor de San Marcos, Museo de Historia Natural. Av. Arenales 1256, Jesús María, Lima, Perú. *Autor para correspondencia Email Joel Vásquez Bardales: [email protected] Email Ricardo Zárate Gómez: [email protected] Email Percy Huiñapi Canaquiri: [email protected] Email Julio Pinedo Jiménez: [email protected] Email Juan José Ramírez Hernández: [email protected] Email Gerardo Lamas: [email protected] Email Pedro Vela García: [email protected] Resumen El presente trabajo informa sobre las plantas alimenticias utilizadas por 19 especies de mariposas diurnas (Lepidoptera) que ocurren en el Centro de Investigaciones Allpahuayo-Mishana y la Comunidad Campesina de San Rafael, Loreto, Perú. Se reportan 23 especies y 1 híbrido de angiospermas empleadas por las mariposas investigadas.
    [Show full text]
  • Final Report for the University of Nottingham / Operation Wallacea Forest Projects, Honduras 2004
    FINAL REPORT for the University of Nottingham / Operation Wallacea forest projects, Honduras 2004 TABLE OF CONTENTS FINAL REPORT FOR THE UNIVERSITY OF NOTTINGHAM / OPERATION WALLACEA FOREST PROJECTS, HONDURAS 2004 .....................................................................................................................................................1 INTRODUCTION AND OVERVIEW ..............................................................................................................................3 List of the projects undertaken in 2004, with scientists’ names .........................................................................4 Forest structure and composition ..................................................................................................................................... 4 Bat diversity and abundance ............................................................................................................................................ 4 Bird diversity, abundance and ecology ............................................................................................................................ 4 Herpetofaunal diversity, abundance and ecology............................................................................................................. 4 Invertebrate diversity, abundance and ecology ................................................................................................................ 4 Primate behaviour...........................................................................................................................................................
    [Show full text]
  • Butterflies of the Golfo Dulce Region Costa Rica
    Butterflies of the Golfo Dulce Region Costa Rica Corcovado National Park Piedras Blancas National Park ‚Regenwald der Österreicher‘ Authors Lisa Maurer Veronika Pemmer Harald Krenn Martin Wiemers Department of Evolutionary Biology Department of Animal Biodiversity University of Vienna University of Vienna Althanstraße 14, 1090 Vienna, Austria Rennweg 14, 1030, Vienna, Austria [email protected] [email protected] Roland Albert Werner Huber Anton Weissenhofer Department of Chemical Ecology Department of Structural and Department of Structural and and Ecosystem Research Functional Botany Functional Botany University of Vienna University of Vienna University of Vienna Rennweg 14, 1030, Vienna, Austria Rennweg 14, 1030, Vienna, Austria Rennweg 14, 1030, Vienna, Austria [email protected] [email protected] [email protected] Contents The ‘Tropical Research Station La Gamba’ 4 The rainforests of the Golfo Dulce region 6 Butterflies of the Golfo Dulce Region, Costa Rica 8 Papilionidae - Swallowtail Butterflies 13 Pieridae - Sulphures and Whites 17 Nymphalidae - Brush Footed Butterflies 21 Subfamily Danainae 22 Subfamily Ithomiinae 24 Subfamily Charaxinae 26 Subfamily Satyrinae 27 Subfamily Cyrestinae 33 Subfamily Biblidinae 34 Subfamily Nymphalinae 35 Subfamily Apaturinae 39 Subfamily Heliconiinae 40 Riodinidae - Metalmarks 47 Lycaenidae - Blues 53 Hesperiidae - Skippers 57 Appendix- Checklist of species 61 Acknowledgements 74 References 74 Picture credits 75 Index 78 3 The ‘Tropical Research Station La Gamba’ Roland Albert Secretary General of the ‘Society for the Preservation of the Tropical Research Station La Gamba’ Department of Chemical Ecology and Ecosystem Research, University of Vienna The main building of the Tropical Research Station In 1991, Michael Schnitzler, a distinguished also provided ideal conditions for promoting musician and former professor at the Univer- Austrian research and teaching programmes in sity of Music and Performing Arts in Vienna, rainforests.
    [Show full text]
  • Annotated Checklist of the Butterflies of Bentsen-Rio Grande Valley State
    AN ANNOTATED CHECKLIST OF THE BUTTERFLIES (LEPIDOPTERA: RHOPALOCERA) OF BENTSEN-RIO GRANDE STATE VALLEY PARK AND VICINITY JUNE, 1974 Published by TEXAS PARKS & WILDLIFE DEPARTMENT BENTSEN-RIO GRANDE VALLEY STATE PARK P.O. 30X 988; MISSION, TEXAS 78572 INTRODUCTION The species listed here in are primarily a result of the collecting by the authors during the period 1972-1973. Certain important records of the previous several years are also included. Additionally, the checklist incorporates records of a number of other lepidopterists. The primary focus of the checklist, then, is upon recent collecting, rather than being an attempt to list all known records from the Mid-Valley area. All lepidopterists collecting in the park and vicinity are urged to send copies of their records to the authors and/or the park authorities. A number of species on the list have been taken in Hidalgo Co. but not yet within the actual confines of the park; the annotations will indicate which species these are. Some of these have been taken at Santa Ana National Wildlife Refuge, approximately thirty miles down river, in habitats similar to those within the park. Others have been taken within several miles of the park, in nearby towns and along roadsides. These species can be reasonably expected to occur in the park, and their inclusion upon this list should alert the collector to their possible presence. The annotations have been kept necessarily brief. They are intended to aid the visiting lepidopterist in evaluating the significance of his catches. Local larval food plants are given where known. Much, however, is still to be learned regarding the life histories of even some of the commoner species.
    [Show full text]
  • 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.
    [Show full text]
  • 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.
    [Show full text]