Nymphalidae, Ithomiinae) from Eastern Ecuador
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Biolphilately Vol-64 No-3
BIOPHILATELY OFFICIAL JOURNAL OF THE BIOLOGY UNIT OF ATA MARCH 2020 VOLUME 69, NUMBER 1 Great fleas have little fleas upon their backs to bite 'em, And little fleas have lesser fleas, and so ad infinitum. —Augustus De Morgan Dr. Indraneil Das Pangolins on Stamps More Inside >> IN THIS ISSUE NEW ISSUES: ARTICLES & ILLUSTRATIONS: From the Editor’s Desk ......................... 1 Botany – Christopher E. Dahle ............ 17 Pangolins on Stamps of the President’s Message .............................. 2 Fungi – Paul A. Mistretta .................... 28 World – Dr. Indraneil Das ..................7 Secretary -Treasurer’s Corner ................ 3 Mammalia – Michael Prince ................ 31 Squeaky Curtain – Frank Jacobs .......... 15 New Members ....................................... 3 Ornithology – Glenn G. Mertz ............. 35 New Plants in the Philatelic News of Note ......................................... 3 Ichthyology – J. Dale Shively .............. 57 Herbarium – Christopher Dahle ....... 23 Women’s Suffrage – Dawn Hamman .... 4 Entomology – Donald Wright, Jr. ........ 59 Rats! ..................................................... 34 Event Calendar ...................................... 6 Paleontology – Michael Kogan ........... 65 New Birds in the Philatelic Wedding Set ........................................ 16 Aviary – Charles E. Braun ............... 51 Glossary ............................................... 72 Biology Reference Websites ................ 69 ii Biophilately March 2020 Vol. 69 (1) BIOPHILATELY BIOLOGY UNIT -
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. -
Chemical Defence of the Warningly Coloured Caterpillars of Methona Themisto (Lepidoptera: Nymphalidae: Ithomiinae)
Eur. J. Entomol. 106: 253–259, 2009 http://www.eje.cz/scripts/viewabstract.php?abstract=1449 ISSN 1210-5759 (print), 1802-8829 (online) Chemical defence of the warningly coloured caterpillars of Methona themisto (Lepidoptera: Nymphalidae: Ithomiinae) KAMILA F. MASSUDA and JOSÉ R. TRIGO* Laboratório de Ecologia Química, Departamento de Zoologia, Instituto de Biologia, Universidade Estadual de Campinas, CP 6109, 13083-970 Campinas, SP, Brazil Key words. Aposematism, Brunfelsia uniflora, Camponotus crassus, Gallus gallus domesticus, learning, Lycosa erythrognatha, predation, Solanaceae, unpalatability Abstract. The caterpillars of the butterfly Methona themisto (Nymphalidae: Ithomiinae) are conspicuously coloured and feed exclu- sively on Brunfelsia uniflora (Solanaceae), a plant that is rich in secondary plant substances, which suggests the caterpillars are chemically protected against predators. Results of experiments indicate that predators determine the survival of Methona themisto caterpillars in the field and laboratory bioassays that this organism is eaten by ants and spiders but not chicks. Both the conspicuous orange and black striped colouration and chemical compounds of Methona themisto caterpillars seem to be related to protection against predation by visually hunting predators. Chicks ate proportionally more of the cryptically coloured 1st instar caterpillars than of the conspicuously coloured later instar caterpillars. That Methona themisto caterpillars are chemically defended is supported by the activity of the dichloromethanic extract of 5th instars in preventing predation by chicks. Caterpillars of Methona themisto are apo- sematic as they are both (1) unpalatable, and (2) their warning signal is easily recognized by potential predators. Chicks learned to avoid the aposematic 3rd or 5th instar caterpillars after one encounter. Mealworms painted to look like caterpillars were also rejected by chicks that had previously encountered Methona caterpillars. -
Journal of the Lepidopterists' Society
Volume 62 Number 2 25 Aug 2008 ISSN 0024-0966 Journal of the Lepidopterists' Society Published quarterly by The Lepidopterists' Society ) ) THE LEPIDOPTERISTS’ SOCIETY Executive Council John H. Acorn, President John Lill, Vice President William E. Conner, Immediate Past President David D. Lavvrie, Secretary Andre V.L. Freitas, Vice President Kelly M. Richers, Treasurer Akito Kayvahara, Vice President Members at large: Kim Garwood Richard A. Anderson Michelle DaCosta Kenn Kaufman John V. Calhoun John H. Masters Plarry Zirlin Amanda Roe Michael G. Pogue Editorial Board John W. Rrovvn {Chair) Michael E. Toliver Member at large ( , Brian Scholtens (Journal Lawrence F. Gall ( Memoirs ) 13 ale Clark {News) John A. Snyder {Website) Honorary Life Members of the Society Charles L. Remington (1966), E. G. Munroe (1973), Ian F. B. Common (1987), Lincoln P Brower (1990), Frederick H. Rindge (1997), Ronald W. Hodges (2004) The object of The Lepidopterists’ Society, which was formed in May 1947 and formally constituted in December 1950, is “to pro- mote the science of lepidopterology in all its branches, ... to issue a periodical and other publications on Lepidoptera, to facilitate the exchange of specimens and ideas by both the professional worker and the amateur in the field; to secure cooperation in all mea- sures” directed towards these aims. Membership in the Society is open to all persons interested in the study of Lepidoptera. All members receive the Journal and the News of The Lepidopterists’ Society. Prospective members should send to the Assistant Treasurer full dues for the current year, to- gether with their lull name, address, and special lepidopterological interests. -
Developmental, Cellular, and Biochemical
Developmental, cellular, and biochemical basis of transparency in the glasswing butterfly Greta oto Aaron Pomerantz, Radwanul Siddique, Elizabeth Cash, Yuriko Kishi, Charline Pinna, Kasia Hammar, Doris Gomez, Marianne Elias, Nipam Patel To cite this version: Aaron Pomerantz, Radwanul Siddique, Elizabeth Cash, Yuriko Kishi, Charline Pinna, et al.. Devel- opmental, cellular, and biochemical basis of transparency in the glasswing butterfly Greta oto. 2020. hal-03012452 HAL Id: hal-03012452 https://hal.archives-ouvertes.fr/hal-03012452 Preprint submitted on 18 Nov 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. bioRxiv preprint doi: https://doi.org/10.1101/2020.07.02.183590; this version posted July 2, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. 1 Title 2 Developmental, cellular, and biochemical basis of transparency in the glasswing butterfly 3 Greta oto 4 5 Authors 6 Aaron F. Pomerantz1,2*, Radwanul H. Siddique3,4, Elizabeth I. Cash5, Yuriko Kishi6,7, 7 Charline Pinna8, Kasia Hammar2, Doris Gomez9, Marianne Elias8, Nipam H. -
Download Articles
QL 541 .1866 ENT The Journal of Research Lepidoptera Volume 46 2013 ISSN 0022 4324 (PRINT) 2156 5457 (ONLINE) THE LEPIDOPTERA RESEARCH FOUNDATION The Journal of Research on the Lepidoptera www.lepidopteraresearchfoundation.org ISSN 0022 4324 (print) 2156 5457 (online) Published by: The Lepidoptera Research Foundation, Inc. 9620 Heather Road Beverly Hills, California 90210-1757 TEL (310) 274 1052 E-mail: Editorial: [email protected] Technical: [email protected] Founder: William Hovanitz (1915-1977) Editorial Staff: Konrad Fiedler, University of Vienna, Editor [email protected] Nancy R. Vannucci, info manager [email protected] Associate Editors: Annette Aiello, Smithsonian Institution [email protected] Joaquin Baixeras, Universitat de Valencia [email protected] Marcelo Duarte, Universidade de Sao Paulo [email protected] Klaus Fischer, University of Greifswald [email protected] Krushnamegh Kunte, Natl. Center for Biol. Sci, India [email protected] Gerardo Lamas, Universidad Mayor de San Marcos [email protected]. pe Rudi Mattoni [email protected] Soren Nylin, Stockholm University [email protected] Naomi Pierce, Harvard University [email protected] Robert Robbins, Smithsonian Institution [email protected] Daniel Rubinoff, University of Hawaii [email protected] Josef Settele, Helmholtz Cntr. for Environ. Research-UFZ [email protected] Arthur M. Shapiro, University of California - Davis [email protected] Felix Sperling, University of Alberta [email protected] Niklas Wahlberg, University of Turku [email protected] Shen Horn Yen, National Sun Yat-Sen University [email protected] Manuscripts and notices material must be sent to the editor, Konrad Fiedler [email protected]. -
Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae)
bs_bs_banner Zoological Journal of the Linnean Society, 2014, 170, 362–399. With 143 figures Phylogeny of Neotropical Castniinae (Lepidoptera: Cossoidea: Castniidae): testing the hypothesis of the mimics as a monophyletic group and implications for the arrangement of the genera SIMEÃO DE SOUZA MORAES1,2* and MARCELO DUARTE2 1Curso de Pós-Graduação em Ciências Biológicas (Zoologia), Instituto de Biociências, Departamento de Zoologia, Universidade de São Paulo, Rua do Matão, travessa 14, número 321, CEP 05508-900, São Paulo, São Paulo, Brazil 2Museu de Zoologia da Universidade de São Paulo, Avenida Nazaré 481, 04263-000, São Paulo, São Paulo, Brazil Received 19 March 2013; revised 11 October 2013; accepted for publication 13 October 2013 A cladistic analysis of the Neotropical Castniidae is presented using 120 morphological characters, and a taxonomic treatment based on that analysis is also presented. The tribe Gazerini as previously delimited was found to be paraphyletic with respect to the genera Ceretes, Divana, Riechia, Frostetola, and Oiticicastnia. The genera Castnia, Geyeria, and Athis were also found to be non-monophyletic taxa. The mimicry pattern had multiple independent origins in the Neotropical castniids, and at least two lineages, Riechia and Prometheus, are involved in Batesian mimicry rings with unpalatable butterfly models in the tribes Acraeini and Heliconiini (Nymphalidae). We propose for Castniini 13 new synonymies and 27 new combinations. Geyeria strigata (Walker, 1854) is revalidated. The generic placements of Athis superba (Strand, 1912) and Castnia eudesmia Gray, 1838 are questionable, but presently upheld. © 2014 The Linnean Society of London, Zoological Journal of the Linnean Society, 2014, 170, 362–399. doi: 10.1111/zoj.12102 ADDITIONAL KEYWORDS: Batesian mimicry – new synonyms – taxonomy. -
Effects of Land Use on Butterfly (Lepidoptera: Nymphalidae) Abundance and Diversity in the Tropical Coastal Regions of Guyana and Australia
ResearchOnline@JCU This file is part of the following work: Sambhu, Hemchandranauth (2018) Effects of land use on butterfly (Lepidoptera: Nymphalidae) abundance and diversity in the tropical coastal regions of Guyana and Australia. PhD Thesis, James Cook University. Access to this file is available from: https://doi.org/10.25903/5bd8e93df512e Copyright © 2018 Hemchandranauth Sambhu The author has certified to JCU that they have made a reasonable effort to gain permission and acknowledge the owners of any third party copyright material included in this document. If you believe that this is not the case, please email [email protected] EFFECTS OF LAND USE ON BUTTERFLY (LEPIDOPTERA: NYMPHALIDAE) ABUNDANCE AND DIVERSITY IN THE TROPICAL COASTAL REGIONS OF GUYANA AND AUSTRALIA _____________________________________________ By: Hemchandranauth Sambhu B.Sc. (Biology), University of Guyana, Guyana M.Sc. (Res: Plant and Environmental Sciences), University of Warwick, United Kingdom A thesis Prepared for the College of Science and Engineering, in partial fulfillment of the requirements for the degree of Doctor of Philosophy James Cook University February, 2018 DEDICATION ________________________________________________________ I dedicate this thesis to my wife, Alliea, and to our little girl who is yet to make her first appearance in this world. i ACKNOWLEDGEMENTS ________________________________________________________ I would like to thank the Australian Government through their Department of Foreign Affairs and Trade for graciously offering me a scholarship (Australia Aid Award – AusAid) to study in Australia. From the time of my departure from my home country in 2014, Alex Salvador, Katherine Elliott and other members of the AusAid team have always ensured that the highest quality of care was extended to me as a foreign student in a distant land. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
Nymphalidae: Ithomiinae)
STUDIES ON THE ECOLOGY AND EVOLUTION OF NEOTROPICAL ITHOMIINE BUTTERFLIES (NYMPHALIDAE: ITHOMIINAE) by GEORGE WILLIAM BECCALONI A thesis submitted for the degree of Doctor ofPhilosophy ofthe University ofLondon October 1995 Biogeography and Conservation Laboratory Centre for Population Biology Department of Entomology Imperial College The Natural History Museum Silwood Park Cromwell Road Ascot London SW7 5BD Berkshire SL5 7PY 2 To my mother, Benjie & Judy in love and gratitude 3 ABSTRACT Two aspects ofthe ecology ofNeotropical ithomiine butterflies (Nymphalidae: Ithomiinae) are discussed: mimicry (Chapters 2, 3) and species richness (Chapters 4, 5). Chapter 2 defines eight mimicry complexes involving ithomiines and other insects found in eastern Ecuador. These complexes are dominated by ithomiine individuals. Hypotheses to explain polymorphism in Batesian and Mullerian mimics are assessed. In Chapter 3, evidence that sympatric ithomiine-dominated mimicry complexes are segregated by microhabitat is reviewed. Data confirm that sympatric complexes are segregated vertically by flight height. Flight height is shown to be positively correlated with larval host-plant height. Host-plant partitioning between species in a butterfly community results in the formation of microhabitat guilds of species, and evidence suggests that mimicry may evolve between species which share a guild, but not between guilds. Models for the evolution of mimicry complexes in sympatry, and for polymorphism and dual sex-limited mimicry in Mullerian mimics, are discussed in the light of these findings. Chapter 4 investigates relationships between species richness offamilies and subfamilies ofNeotropical butterflies and overall butterfly species richness at local and regional scales. A strong positive correlation is demonstrated between ithomiine richness and the species richness of all other butterflies. -
Mimicry Some Heliconius (Heliconiinae) from Peru and Colombia, So He Assumed the Resemblance Was the Result of Some Inorganic Mathieu Joron Or Environmental Factors
Preprint for: Joron, M. 2003. In Encyclopedia of insects (R. T. Cardé & V. H. Resh, eds), pp. 714-726. Academic Press, New York. Melinaea, Mechanitis (Ithomiinae), Lycorea (Danainae), and Mimicry some Heliconius (Heliconiinae) from Peru and Colombia, so he assumed the resemblance was the result of some inorganic Mathieu Joron or environmental factors. In 1879, German naturalist Fritz Leiden University, The Netherlands Müller was the first to develop a mathematical demonstration that two unpalatable prey could benefit from mutual resem- imicry is the adaptive resemblance in signal be- blance. He understood that, if the community of predators tween several species in a locality. The most had to kill a certain (fixed) number of prey to learn to avoid M spectacular and intriguing cases are of course them, two indistinguishable distasteful species would to- those of accurate resemblance between distantly related spe- gether suffer this mortality and both reduce their death rate cies, such as spiders mimicking ants. Closely related animals per unit time. Müller actually showed that this benefit was can also benefit from mutual resemblance, in which case biased in favor of the rarer species, to a factor equal to the mimicry results from selection against signal divergence. square of the ratio of the species’ abundance. Therefore, un- equal population sizes translate into even more unequal, The vast majority of the hundreds of thousands of insect spe- although still mutual, benefits: Müllerian mimicry, thus de- cies are described and identifiable on the basis of fined, could be beneficial for both species, and perhaps also morphological characters. This bewildering diversity is, how- for the predators, in contrast to parasitic Batesian mimicry. -
The Genus Adelpha 231
The Genus Adelpha 231 PLATE 1 (pp. 50-63). Figs. 32-38, a,c,e,g, dorsal surface; b,d,f,h, ventral surface. 32a,b: A. bredowii bredowii, Mexico; c,d: A. bredowii eulalia, USA; e,f: A. bredowii californica, USA. 33a,b: A. diocles diocles, Panama; c,d: A. diocles creton, Mexico. 34a,b: A. herbita, S.E. Brazil. 35a,b: A. zea, S.E. Brazil. 36a,b: A. paroeca paroeca, Mexico; c,d: A. paroeca paroeca, Panama. 37a,b: A. nea nea, E. Ecuador; c,d: A. nea sentia, Belize. 38a,b: A. paraena paraena, E. Ecuador; c,d: A. paraena lecromi, W. Colombia; e,f: A. paraena reyi, Venezuela; g,h: A. paraena massilia, Costa Rica. 232 The Genus Adelpha PLATE 2 (pp. 63-76). Figs. 39-41l, a,c,e,g,i,k, dorsal surface; b,d,f,h,j,l, ventral surface. 39a,b: A. radiata radiata, S.E. Brazil; c,d: A. radiata myrlea, S. E. Brazil; e,f: A. radiata explicator, E. Ecuador; g,h: A. radiata aiellae, W. Ecuador; i,j: A. radiata gilletella, French Guiana. 40a,b: A. serpa serpa, S.E. Brazil; c,d: A. serpa diadochus, Peru; e,f: A. serpa celerio, Guatemala; g,h: A. serpa duiliae, W. Ecuador. 41a,b: A. seriphia seriphia, no locality; c,d: A. seriphia pione, Venezuela; e,f: A. seriphia aquillia, E. Ecuador; g,h: A. seriphia godmani, Mexico; i,j: A. seriphia therasia, Bolivia; k,l: A. seriphia egregia, N. Colombia. The Genus Adelpha 233 PLATE 3 (pp. 76-78).