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Checklist of Fish and Invertebrates Listed in the CITES Appendices
JOINTS NATURE \=^ CONSERVATION COMMITTEE Checklist of fish and mvertebrates Usted in the CITES appendices JNCC REPORT (SSN0963-«OStl JOINT NATURE CONSERVATION COMMITTEE Report distribution Report Number: No. 238 Contract Number/JNCC project number: F7 1-12-332 Date received: 9 June 1995 Report tide: Checklist of fish and invertebrates listed in the CITES appendices Contract tide: Revised Checklists of CITES species database Contractor: World Conservation Monitoring Centre 219 Huntingdon Road, Cambridge, CB3 ODL Comments: A further fish and invertebrate edition in the Checklist series begun by NCC in 1979, revised and brought up to date with current CITES listings Restrictions: Distribution: JNCC report collection 2 copies Nature Conservancy Council for England, HQ, Library 1 copy Scottish Natural Heritage, HQ, Library 1 copy Countryside Council for Wales, HQ, Library 1 copy A T Smail, Copyright Libraries Agent, 100 Euston Road, London, NWl 2HQ 5 copies British Library, Legal Deposit Office, Boston Spa, Wetherby, West Yorkshire, LS23 7BQ 1 copy Chadwick-Healey Ltd, Cambridge Place, Cambridge, CB2 INR 1 copy BIOSIS UK, Garforth House, 54 Michlegate, York, YOl ILF 1 copy CITES Management and Scientific Authorities of EC Member States total 30 copies CITES Authorities, UK Dependencies total 13 copies CITES Secretariat 5 copies CITES Animals Committee chairman 1 copy European Commission DG Xl/D/2 1 copy World Conservation Monitoring Centre 20 copies TRAFFIC International 5 copies Animal Quarantine Station, Heathrow 1 copy Department of the Environment (GWD) 5 copies Foreign & Commonwealth Office (ESED) 1 copy HM Customs & Excise 3 copies M Bradley Taylor (ACPO) 1 copy ^\(\\ Joint Nature Conservation Committee Report No. -
Hymenoptera: Trichogrammatidae), T
bioRxiv preprint doi: https://doi.org/10.1101/493643; this version posted December 13, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity.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 Description and biology of two new egg parasitoid species, 2 Trichogramma chagres and T. soberania (Hymenoptera: 3 Trichogrammatidae) reared from eggs of Heliconiini 4 butterflies (Lepidoptera: Nymphalidae: Heliconiinae) 5 collected in Panama 6 7 Jozef B. Woelke1,2, Viktor N. Fursov3, Alex V. Gumovsky3, Marjolein de Rijk1,4, Catalina 8 Estrada5, Patrick Verbaarschot1, Martinus E. Huigens1,6 and Nina E. Fatouros1,7 9 10 1 Laboratory of Entomology, Wageningen University & Research, P.O. Box 16, 6700 AA, 11 Wageningen, The Netherlands. 12 2 Current address: Business Unit Greenhouse Horticulture, Wageningen University & 13 Research, P.O. Box 20, 2665 Z0G, Bleiswijk, The Netherlands. 14 3 Schmalhausen Institute of Zoology of National Academy of Sciences of Ukraine, Bogdan 15 Khmel’nitskiy Street 15, 01601, Kiev, Ukraine. 16 4 Faculty of Science, Radboud University, P.O. Box 9010, 6500 GL, Nijmegen, The 17 Netherlands. 18 5 Imperial College London, Silwood Park campus, Buckhurst road, SL5 7PY, Ascot, UK. 19 6 Current address: Education Institute, Wageningen University & Research, P.O. Box 59, 20 6700 AB, Wageningen, The Netherlands. bioRxiv preprint doi: https://doi.org/10.1101/493643; this version posted December 13, 2018. 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. -
INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a Synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a Historical Sketch
ZOOLOGÍA-TAXONOMÍA www.unal.edu.co/icn/publicaciones/caldasia.htm Caldasia 31(2):407-440. 2009 HACIA UNA SÍNTESIS DE LOS PAPILIONOIDEA (INSECTA: LEPIDOPTERA) DE GUATEMALA CON UNA RESEÑA HISTÓRICA Towards a synthesis of the Papilionoidea (Insecta: Lepidoptera) from Guatemala with a historical sketch JOSÉ LUIS SALINAS-GUTIÉRREZ El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] CLAUDIO MÉNDEZ Escuela de Biología, Universidad de San Carlos, Ciudad Universitaria, Campus Central USAC, Zona 12. Guatemala, Guatemala. [email protected] MERCEDES BARRIOS Centro de Estudios Conservacionistas (CECON), Universidad de San Carlos, Avenida La Reforma 0-53, Zona 10, Guatemala, Guatemala. [email protected] CARMEN POZO El Colegio de la Frontera Sur (ECOSUR). Unidad Chetumal. Av. Centenario km. 5.5, A. P. 424, C. P. 77900. Chetumal, Quintana Roo, México, México. [email protected] JORGE LLORENTE-BOUSQUETS Museo de Zoología, Facultad de Ciencias, UNAM. Apartado Postal 70-399, México D.F. 04510; México. [email protected]. Autor responsable. RESUMEN La riqueza biológica de Mesoamérica es enorme. Dentro de esta gran área geográfi ca se encuentran algunos de los ecosistemas más diversos del planeta (selvas tropicales), así como varios de los principales centros de endemismo en el mundo (bosques nublados). Países como Guatemala, en esta gran área biogeográfi ca, tiene grandes zonas de bosque húmedo tropical y bosque mesófi lo, por esta razón es muy importante para analizar la diversidad en la región. Lamentablemente, la fauna de mariposas de Guatemala es poco conocida y por lo tanto, es necesario llevar a cabo un estudio y análisis de la composición y la diversidad de las mariposas (Lepidoptera: Papilionoidea) en Guatemala. -
BUTTERFLIES in Thewest Indies of the Caribbean
PO Box 9021, Wilmington, DE 19809, USA E-mail: [email protected]@focusonnature.com Phone: Toll-free in USA 1-888-721-3555 oror 302/529-1876302/529-1876 BUTTERFLIES and MOTHS in the West Indies of the Caribbean in Antigua and Barbuda the Bahamas Barbados the Cayman Islands Cuba Dominica the Dominican Republic Guadeloupe Jamaica Montserrat Puerto Rico Saint Lucia Saint Vincent the Virgin Islands and the ABC islands of Aruba, Bonaire, and Curacao Butterflies in the Caribbean exclusively in Trinidad & Tobago are not in this list. Focus On Nature Tours in the Caribbean have been in: January, February, March, April, May, July, and December. Upper right photo: a HISPANIOLAN KING, Anetia jaegeri, photographed during the FONT tour in the Dominican Republic in February 2012. The genus is nearly entirely in West Indian islands, the species is nearly restricted to Hispaniola. This list of Butterflies of the West Indies compiled by Armas Hill Among the butterfly groupings in this list, links to: Swallowtails: family PAPILIONIDAE with the genera: Battus, Papilio, Parides Whites, Yellows, Sulphurs: family PIERIDAE Mimic-whites: subfamily DISMORPHIINAE with the genus: Dismorphia Subfamily PIERINAE withwith thethe genera:genera: Ascia,Ascia, Ganyra,Ganyra, Glutophrissa,Glutophrissa, MeleteMelete Subfamily COLIADINAE with the genera: Abaeis, Anteos, Aphrissa, Eurema, Kricogonia, Nathalis, Phoebis, Pyrisitia, Zerene Gossamer Wings: family LYCAENIDAE Hairstreaks: subfamily THECLINAE with the genera: Allosmaitia, Calycopis, Chlorostrymon, Cyanophrys, -
Heliconinos De La Colección Entomológica De La Facultad De Ciencias Agronómicas, Villaflores, Chiapas, México
ISSN: 2448-4768 Bol. Soc. Mex. Ento. (n. s.) Número especial 2: 34−38 2016 HELICONINOS DE LA COLECCIÓN ENTOMOLÓGICA DE LA FACULTAD DE CIENCIAS AGRONÓMICAS, VILLAFLORES, CHIAPAS, MÉXICO Ricardo Cabrera-Lopez*, Carlos J. Morales-Morales, Eduardo Aguilar-Astudillo y Julio C. Gómez-Castañeda. Universidad Autónoma de Chiapas, Facultad de Ciencias Agronómicas, Campus V, Carret. Ocozocoautla- Villaflores, km 84, C. P. 30470, Villaflores, Chiapas, México. *Autor para correspondencia: cabrera9328 @hotmail.com Recibido: 15/03/2016; Aceptado: 24/04/2016 RESUMEN: El trabajo se realizó en la Colección Entomológica de la Facultad de Ciencias Agronómicas, Campus V de la Universidad Autónoma de Chiapas (FCA-CV) con el material entomológico de la Subfamilia Heliconiinae Swainson, 1822 (Lepidoptera: Nymphalidae), de las cuales se revisaron 202 ejemplares representados en ocho géneros y 16 especies. El género mejor representado fue Heliconius con 68 ejemplares con siete especies: Heliconius charitonia vazquezae Comstock y Brown, 1950; Heliconius erato petiverana (Doubleday, 1847); Heliconius hecale fornarina Hewitson, 1854; Heliconius hecalesia octavia Bates, 1866; Heliconius hortense Guérin-Méneville, 1844; Heliconius ismenius telchinia Doubleday, 1847 y Heliconius sapho leuce Doubleday, 1857. Las especies mejor representadas son Dryas iulia moderata (Rilet, 1926), H. charitonia vazquezae, Agraulis vanillae incarnata (Riley, 1926), Dione juno huascuma (Reakirt, 1966) y Eueides isabella eva (Fabricius, 1793). Los organismos se encuentran depositados en la colección entomológica. Las especies H. hecalesia octavia y Laparus doris transiens Staudinger, 1896 están representadas únicamente por un ejemplar. El estatus de sobrevivencia de H. hecalesia octavia se encuentra presionado en Chiapas debido a los cambios drásticos en los bosques causados por las actividades antropológicas. -
Molecular Phylogeny and Systematics of the Pieridae (Lepidoptera: Papilionoidea): Higher Classification and Biogeography
Blackwell Publishing LtdOxford, UKZOJZoological Journal of the Linnean Society0024-4082The Lin- nean Society of London, 2006? 2006 147? 239275 Original Article PHYLOGENY AND SYSTEMATICS OF THE PIERIDAEM. F. BRABY ET AL. Zoological Journal of the Linnean Society, 2006, 147, 239–275. With 8 figures Molecular phylogeny and systematics of the Pieridae (Lepidoptera: Papilionoidea): higher classification and Downloaded from https://academic.oup.com/zoolinnean/article-abstract/147/2/239/2631026 by Harvard Library user on 21 November 2018 biogeography MICHAEL F. BRABY1,2*, ROGER VILA1 and NAOMI E. PIERCE1 1Museum of Comparative Zoology, Harvard University, 26 Oxford St, Cambridge, MA 02138, USA 2School of Botany and Zoology, The Australian National University, Canberra, ACT 0200, Australia Received May 2004; accepted for publication October 2005 The systematic relationships of the butterfly family Pieridae are poorly understood. Much of our current under- standing is based primarily on detailed morphological observations made 50–70 years ago. However, the family and its putative four subfamilies and two tribes, have rarely been subjected to rigorous phylogenetic analysis. Here we present results based on an analysis of molecular characters used to reconstruct the phylogeny of the Pieridae in order to infer higher-level classification above the generic level and patterns of historical biogeography. Our sample contained 90 taxa representing 74 genera and six subgenera, or 89% of all genera recognized in the family. Three complementary approaches were -
Butterflies and Moths of Dominican Republic
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 -
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. -
Lepidoptera, Nymphalidae) Do Rio Grande
O estágio de ovo dos Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande... 29 O estágio de ovo dos Heliconiini (Lepidoptera, Nymphalidae) do Rio Grande do Sul, Brasil1 Rafael Dell’Erba2, 3, Lucas A. Kaminski4 & Gilson R. P. Moreira4 1. Contribuição no 453 do Departamento de Zoologia da Universidade Federal do Rio Grande do Sul, Porto Alegre, RS, Brasil. 2. PPG Entomologia, Departamento de Zoologia, Universidade Federal do Paraná, Caixa Postal 19020, 81531-990 Curitiba, PR, Brasil. 3. Departamento de Ciências Biológicas, Universidade do Estado de Mato Grosso, Caixa Postal 08, 78690-000 Nova Xavantina, MT, Brasil. ([email protected]) 4. Departamento de Zoologia, Instituto de Biociências, Universidade Federal do Rio Grande do Sul, Av. Bento Gonçalves, 9500, 91501-970 Porto Alegre, RS, Brasil. ([email protected], [email protected]) ABSTRACT. The egg stage of Heliconiini (Lepidoptera, Nymphalidae) from Rio Grande do Sul, Brazil. Based upon light and scanning electron microscopy, the external morphology of the egg stage is described and illustrated for the following Heliconiini (Lepidoptera, Nymphalidae) from Rio Grande do Sul State, Brazil: Agraulis vanillae maculosa (Stichel, 1907), Dione juno juno (Cramer, 1779), Dione moneta moneta Hübner, 1825, Dryadula phaetusa (Linnaeus, 1758), Dryas iulia alcionea (Cramer, 1779), Philaethria wernickei (Röber, 1906), Eueides isabella dianasa (Hübner, 1806), Eueides aliphera aliphera (Godart, 1819), Heliconius ethilla narcaea Godart, 1819, Heliconius besckei Ménétriés, 1857, and Heliconius erato phyllis (Fabricius, 1775). A dichotomic key is provided for their identification, based upon differences at the levels of generic and ultrastructural morphology, and variation in host-plant use. KEYWORDS. Chorionic ultrastructure, egg morphology, heliconian butterflies, host-plants. -
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. -
Do Pollen Feeding, Pupal-Mating and Larval Gregariousness Have a Single Origin in Heliconius Butterflies? Inferences from Multilocus DNA Sequence Data
Biological Journal of the Linnean Society, 2007, 92, 221-239. With 4 figures Do pollen feeding, pupal-mating and larval gregariousness have a single origin in Heliconius butterflies? Inferences from multilocus DNA sequence data MARGAEITA BELTRAN1'2'3*, CHRIS D. JIGGINS3, ANDREW V. Z. BROWER4, ELDREDGE BERMINGHAM1 and JAMES MALLET2 Smithsonian Tropical Research Institute, AA 2072, Balboa, Panama 2The Galton Laboratory, Department of Biology, University College London, London NW1 2HE, UK ^Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK department of Biology, Middle Tennessee State University, Murfreesboro, TN 37132, USA Received 22 November 2005; accepted for publication 4 November 2006 Phylogenetic information is useful in understanding the evolutionary history of adaptive traits. Here, we present a well-resolved phylogenetic hypothesis for Heliconius butterflies and related genera. We use this tree to investigate the evolution of three traits, pollen feeding, pupal-mating behaviour and larval gregariousness. Phylogenetic relationships among 60 Heliconiina species (86% of the subtribe) were inferred from partial DNA sequences of the mitochondrial genes cytochrome oxidase I, cytochrome oxidase II and 16S rRNA, and fragments of the nuclear genes elongation factor-la, apterous, decapentaplegic and wingless (3834 bp in total). The results corroborate previous hypotheses based on sequence data in showing that Heliconius is paraphyletic, with Laparus doris and Neruda falling within the genus, demonstrating a single origin for pollen feeding but with a loss of the trait in Neruda. However, different genes are not congruent in their placement of Neruda; therefore, monophyly of the pollen feeding species cannot be ruled out. There is also a highly supported monophyletic 'pupal-mating clade' suggesting that pupal mating behaviour evolved only once in the Heliconiina. -
The Butterflies (Lepidoptera, Papilionoidea) of Tobago, West
INSECTA MUNDI A Journal of World Insect Systematics 0539 The butterfl ies (Lepidoptera, Papilionoidea) of Tobago, West Indies: An updated and annotated checklist Matthew J.W. Cock CABI, Bakeham Lane Egham, Surrey, TW20 9TY United Kingdom Date of Issue: April 28, 2017 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Matthew J.W. Cock The butterfl ies (Lepidoptera, Papilionoidea) of Tobago, West Indies: An updated and annotated checklist Insecta Mundi 0539: 1–38 ZooBank Registered: urn:lsid:zoobank.org:pub:B96122B2-6325-4D7F-A260-961BB086A2C5 Published in 2017 by Center for Systematic Entomology, Inc. P. O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non-marine arthropod. Topics considered for publication include systematics, taxonomy, nomenclature, checklists, faunal works, and natural history. Insecta Mundi will not consider works in the applied sciences (i.e. medical entomology, pest control research, etc.), and no longer publishes book reviews or editorials. Insecta Mundi publishes original research or discoveries in an inexpensive and timely manner, distributing them free via open access on the internet on the date of publication. Insecta Mundi is referenced or abstracted by several sources including the Zoological Record, CAB Ab- stracts, etc. Insecta Mundi is published irregularly throughout the year, with completed manuscripts assigned an individual number. Manuscripts must be peer reviewed prior to submission, after which they are reviewed by the editorial board to ensure quality. One author of each submitted manuscript must be a current member of the Center for Systematic Entomology.