Papilionidae Biosecurity Occurrence Background Subfamilies Short Description Diagnosis
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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. -
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. -
Phylogeny and Evolution of Lepidoptera
EN62CH15-Mitter ARI 5 November 2016 12:1 I Review in Advance first posted online V E W E on November 16, 2016. (Changes may R S still occur before final publication online and in print.) I E N C N A D V A Phylogeny and Evolution of Lepidoptera Charles Mitter,1,∗ Donald R. Davis,2 and Michael P. Cummings3 1Department of Entomology, University of Maryland, College Park, Maryland 20742; email: [email protected] 2Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC 20560 3Laboratory of Molecular Evolution, Center for Bioinformatics and Computational Biology, University of Maryland, College Park, Maryland 20742 Annu. Rev. Entomol. 2017. 62:265–83 Keywords Annu. Rev. Entomol. 2017.62. Downloaded from www.annualreviews.org The Annual Review of Entomology is online at Hexapoda, insect, systematics, classification, butterfly, moth, molecular ento.annualreviews.org systematics This article’s doi: Access provided by University of Maryland - College Park on 11/20/16. For personal use only. 10.1146/annurev-ento-031616-035125 Abstract Copyright c 2017 by Annual Reviews. Until recently, deep-level phylogeny in Lepidoptera, the largest single ra- All rights reserved diation of plant-feeding insects, was very poorly understood. Over the past ∗ Corresponding author two decades, building on a preceding era of morphological cladistic stud- ies, molecular data have yielded robust initial estimates of relationships both within and among the ∼43 superfamilies, with unsolved problems now yield- ing to much larger data sets from high-throughput sequencing. Here we summarize progress on lepidopteran phylogeny since 1975, emphasizing the superfamily level, and discuss some resulting advances in our understanding of lepidopteran evolution. -
Natural History of Fiji's Endemic Swallowtail Butterfly, Papilio Schmeltzi
32 TROP. LEPID. RES., 23(1): 32-38, 2013 CHANDRA ET AL.: Life history of Papilio schmeltzi NATURAL HISTORY OF FIJI’S ENDEMIC SWALLOWTAIL BUTTERFLY, PAPILIO SCHMELTZI (HERRICH-SCHAEFFER) Visheshni Chandra1, Uma R. Khurma1 and Takashi A. Inoue2 1School of Biological and Chemical Sciences, Faculty of Science, Technology and Environment, The University of the South Pacific, Private Bag, Suva, Fiji. Correspondance: [email protected]; 2Japanese National Institute of Agrobiological Sciences, Ôwashi 1-2, Tsukuba, Ibaraki, 305-8634, Japan Abstract - The wild population of Papilio schmeltzi (Herrich-Schaeffer) in the Fiji Islands is very small. Successful rearing methods should be established prior to any attempts to increase numbers of the natural population. Therefore, we studied the biology of this species. Papilio schmeltzi was reared on Micromelum minutum. Three generations were reared during the period from mid April 2008 to end of November 2008, and hence we estimate that in nature P. schmeltzi may have up to eight generations in a single year. Key words: Papilio schmeltzi, Micromelum minutum, life cycle, larval host plant, developmental duration, morphological characters, captive breeding INTRODUCTION MATERIALS AND METHODS Most of the Asia-Pacific swallowtail butterflies P. schmeltzi was reared in a screened enclosure from mid (Lepidopera: Papilionidae) belonging to the genus Papilio are April 2008 to end of November 2008. The enclosure was widely distributed in the tropics (e.g. Asia, Papua New Guinea, designed to provide conditions as close to its natural habitat as Australia, New Caledonia, Vanuatu, Solomon Islands, Fiji and possible and was located in an open area at the University of Samoa). -
Whole Genome Shotgun Phylogenomics Resolves the Pattern
Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution Rémi Allio, Celine Scornavacca, Benoit Nabholz, Anne-Laure Clamens, Felix Sperling, Fabien Condamine To cite this version: Rémi Allio, Celine Scornavacca, Benoit Nabholz, Anne-Laure Clamens, Felix Sperling, et al.. Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution. Systematic Biology, Oxford University Press (OUP), 2020, 69 (1), pp.38-60. 10.1093/sysbio/syz030. hal-02125214 HAL Id: hal-02125214 https://hal.archives-ouvertes.fr/hal-02125214 Submitted on 10 May 2019 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. Running head Shotgun phylogenomics and molecular dating Title proposal Downloaded from https://academic.oup.com/sysbio/advance-article-abstract/doi/10.1093/sysbio/syz030/5486398 by guest on 07 May 2019 Whole genome shotgun phylogenomics resolves the pattern and timing of swallowtail butterfly evolution Authors Rémi Allio1*, Céline Scornavacca1,2, Benoit Nabholz1, Anne-Laure Clamens3,4, Felix -
Scientific Name Common Name Distribution, Notes Food Plant Family PAPILIONIDAE: 51 Species SWALLOWTAILS
Scientific Name Common Name Distribution, notes Food Plant Family PAPILIONIDAE: 51 species SWALLOWTAILS Subfamily Baroniinae: 1 species Baronia Baronia brevicornis brevicornis Baronia Baronia brevicornis rufodiscalis Baronia Chiapas Subfamily Papilioninae: 50 species Battus philenor philenor Pipevine Swallowtail Battus philenor acauda 'Yucatan' Pipevine Swallowtail Yucatan Peninsula and surrounding areas Battus philenor orsua 'Tres Marias' Pipevine Swallowtail Islas Tres Marias, Nayarit Battus philenor insularis 'Revillagigedo' Pipevine Swallowtail Islas Revillagigedo, Colima Battus polydamas polydamas Polydamas Swallowtail Battus eracon West-Mexican Swallowtail Battus laodamas iopas Green-patch Swallowtail W Mexico Battus laodamas copanae Green-patch Swallowtail E Mexico Battus ingenuus Dyar's Swallowtail Battus lycidas Cramer's Swallowtail Parides alopius White-dotted Cattleheart Parides photinus Pink-spotted Cattleheart Parides montezuma Montezuma’s Cattleheart Parides eurimedes mylotes True Cattleheart Parides childrenae childrenae Green-celled Cattleheart Parides sesostris zestos Emerald-patched Cattleheart Parides panares panares Wedge-spotted Cattleheart Oaxaca Parides panares lycimenes Wedge-spotted Cattleheart Chiapas, etc. Parides erithalion polyzelus Variable Cattleheart E Mexico Parides erithalion trichopus Variable Cattleheart W Mexico Parides iphidamas iphidamas Iphidamas Cattleheart Parides anchises marthilia Chiapas Cattleheart Eurytides epidaus epidaus Mexican Kite-Swallowtail E Mexico Eurytides epidaus fenochionis Mexican -
The Signal Environment Is More Important Than Diet Or Chemical Specialization in the Evolution of Warning Coloration
The signal environment is more important than diet or chemical specialization in the evolution of warning coloration Kathleen L. Prudic†‡, Jeffrey C. Oliver§, and Felix A. H. Sperling¶ †Department of Ecology and Evolutionary Biology and §Interdisciplinary Program in Insect Science, University of Arizona, Tucson, AZ 85721; and ¶Department of Biological Sciences, University of Alberta, Edmonton, AB, Canada T6G 2E9 Edited by May R. Berenbaum, University of Illinois at Urbana–Champaign, Urbana, IL, and approved October 11, 2007 (received for review June 13, 2007) Aposematic coloration, or warning coloration, is a visual signal that in ref. 13). Prey can become noxious by consuming other organisms acts to minimize contact between predator and unprofitable prey. with defensive compounds (e.g., refs. 15 and 16). By specializing on The conditions favoring the evolution of aposematic coloration re- a particular toxic diet, the consumer becomes noxious and more main largely unidentified. Recent work suggests that diet specializa- likely to evolve aposematic coloration as a defensive strategy tion and resultant toxicity may play a role in facilitating the evolution (reviewed in ref. 13). Diet specialization, in which a consumer feeds and persistence of warning coloration. Using a phylogenetic ap- on a limited set of related organisms, allows the consumer to tailor proach, we investigated the evolution of larval warning coloration in its metabolism to efficiently capitalize on the specific toxins shared the genus Papilio (Lepidoptera: Papilionidae). Our results indicate that by a suite of related hosts. Recent investigations suggest that diet there are at least four independent origins of aposematic larval specialization on toxic organisms promotes the evolution of apose- coloration within Papilio. -
Doterra Essential Oils Scientific References Bibliography The
doTERRA Essential Oils Scientific References Bibliography The Science of Aroma and Touch 1. Hertenstein M, et al. Touch communicates distinct emotions. Emotion. 2006;6(3):528-533. 2. Thompson E. and Hampton J. The effect of relationship status on communicating emotions through touch. Cognition and Emotion. 2011; 25(2):295-306. 3. Chatel-Goldman J, et al. Touch increases autonomic coupling between romantic partners. Frontiers in Behavioral Neuroscience. 2014; 8:95. 4. Uvnas-Moberg, K, et al. Self-soothing behaviors with particular reference to oxytocin release induced by non- noxious sensory stimulation. Frontiers in Psychology. 2014; 5:1529. The Science of Cypress 1. M. Kusuhara, K. Urakami, Y. Masuda, V. Zangiacomi, H. Ishii, S. Tai, K. Maruyama, and K. Yamaguchi, “Fragrant environment with α-pinene decreases tumor growth in mice,” Biomed. Res. Tokyo Jpn., vol. 33, no. 1, pp. 57–61, Feb. 2012. 2. H. J. Dorman and S. G. Deans, “Antimicrobial agents from plants: antibacterial activity of plant volatile oils,” J. Appl. Microbiol., vol. 88, no. 2, pp. 308–316, Feb. 2000. Chemistry of Pink Pepper 1. Siqueira HDS, Neto BS, Sousa DP, et al. α-Phellandrene, a cyclic monoterpene, attenuates inflammatory response through neutrophil migration inhibition and mast cell degranulation. Life Sci. 2016;160:27-33. doi:10.1016/j.lfs. 2016.07.008 2. Lin J-J, Lin J-H, Hsu S-C, et al. Alpha-phellandrene promotes immune responses in normal mice through enhancing macrophage phagocytosis and natural killer cell activities. Vivo Athens Greece. 2013;27(6):809-814. 3. Jing L, Zhang Y, Fan S, et al. -
Comparison of Rainforest Butterfly Assemblages Across Three Biogeographical Regions Using Standardized Protocols
The Journal Volume 44: 17-28 of Research on the Lepidoptera ISSN 0022-4324 (PR in T ) THE LEPIDOPTERA RESEARCH FOUNDATION, 4 MA Y 2011 ISSN 2156-5457 (O N L in E ) Comparison of rainforest butterfly assemblages across three biogeographical regions using standardized protocols YVE S Bass ET 1,*, RO D Eas TWOO D 2, LEG I Sam 3, DA V id J. LO hman 2,4, VO J TE ch NOVOT N Y 5, Tim TRE U ER 2, SC OTT E. MI LLER 6, GEORGE D. WE ib LE N 7, NA O mi E. PI ER C E 2, SA R A Y udh Bun Y A VE jch EW in 8, WA T ana SA K ch OOWO N G 8, PI TOO N KO N G N OO 9 and MI G U EL A. OS OR I O -ARE nas 1 1Smithsonian Tropical Research Institute, Apartado 0843-03092, Balboa, Ancon, Panama City, Republic of Panama 2Museum of Comparative Zoology, Harvard University, 26 Oxford Street, Cambridge, MA 02138, USA 3The New Guinea Binatang Research Center, PO Box 604, Madang, Papua New Guinea 4Department of Biology, The City College of New York, The City University of New York, Convent Avenue at 138th Street, New York, NY 10031, USA 5Biology Center of the Czech Academy of Sciences and School of Biological Sciences, University of South Bohemia, Branisovska 31, 370 05 Ceske Budejovice, Czech Republic 6National Museum of Natural History, Smithsonian Institution, Washington, DC 20560-0105, USA 7Bell Museum of Natural History, University of Minnesota, 250 Biological Sciences Center, 1445 Gortner Avenue Saint Paul, Minnesota 55108, USA 8Thai National Parks Wildlife and Plant Conservation Department, 61 Phaholyothin Road, Chatuchak, Bangkok 10900, Thailand 9Center for Tropical Forest Science, Khao Chong Botanical Garden, Tambon Chong, Nayong District, Trang 92170, Thailand [email protected] Abstract. -
Characteristics of Butterfly (Lepidoptera) Fauna from Kabal
Journal of Entomology and Zoology Studies 2014; 2 (1): 56-69 Characteristics of butterfly (Lepidoptera) fauna from ISSN 2320-7078 Kabal, Swat, Pakistan JEZS 2014; 2 (1): 56-69 © 2014 JEZS Received 30-12-2013 Accepted: 13-01-2014 Farzana Perveen*, Anzela Khan, Sikander ABSTRACT The beautiful creature of nature, butterflies (Lepidoptera) have great aesthetic and commercial values Dr Farzana Perveen as they are beneficial as pollinator and environmental indicator. The present survey was conducted to Founder Chairperson and Associate determine the characteristics of butterfly fauna from Kabal, Swat, Pakistan during March-June 2013. Professor, Department of Zoology; The study area was divided into 4 quadrates. A total of 170 specimens were collected 13 species, Controller of Examinations, Shaheed falling in 10 genera and were identified belonging to 3 different families. The species identified, the Benazir Bhutto University (SBBU), Indian fritillary (Argynnis hyperbius) (Linnaeus, 1763) (female and male); painted lady (Cynthia Main Campus, Sheringal, Khyber cardui) (Linnaeus, 1758); blue pansy (Junonia orithya) Linnaeus, 1758; plain tiger (Danaus Pakhtunkhwa, Pakistan chrysippus) (Linnaeus, 1758); common leopard (Phalantha phalantha) (Drury, 1773) and common Tel: (092)-944-885529 sailor butterfly (Neptis hylas) (Linnaeus, 1758) were belonging to family Nymphalidae. The great E-mail: [email protected] black mormon (Papilio memnon) Linnaeus, 1758; Chinese peacock black swallowtail emerald (Papilio bianor) Cramer, 1777; dingy swallowtail (Papilio anactus) Macleay, 1826 and lime Anzela Khan Beaconhouse School System, butterfly (Papilio demoleus) Linnaeus, 1758 were belonging to family Papilionidae. The common Margalla Campus, H-8, (BMI-G); grass yellow (Eumera hecab) (Linnaeus, 1758); little orange tip (Coloti etrida) (Boisduval, 1836) and Pakistan Murree green-veined white (Pieris ajaka) Moore 1865 were belonging to family Pieridae. -
Table of Contents
SUPPLEMENTARY MATERIAL Volatile Terpenes and Terpenoids from the Workers and Queens of Monomorium chinense (Hymenoptera: Formicidae) Rui Zhao 1, 2, Lihua Lu 2, Qingxing Shi 2, Jian Chen 3*, Yurong He 1* 1 Department of Entomology, College of Agriculture, South China Agricultural University, Tianhe District, Guangzhou, Guangdong 510642, China; [email protected] (R.Z.) 2 Plant Protection Research Institute, Guangdong Academy of Agricultural Sciences, Tianhe District, Guangzhou, Guangdong 510640, China; [email protected] (L.L.); [email protected] (Q.S.) 3 National Biological Control Laboratory, Southeast Area, Agriculture Research Service, United States Department of Agriculture, 59 Lee Road, Stoneville, MS 38776, USA *Correspondence: [email protected] (J.C.); [email protected] (Y.H.) Table of Contents Figure S1 Mass spectrum of peak 1 (a) from Monomorium chinense workers and δ-elemene (b) from the literature book, showing the match of mass spectra. .......................................................... 3 Figure S2 Total ion chromatograms of extract of Monomorium chinense workers (a) and standard β-elemene (b), showing the match of retention times; Mass spectra of peak 2(c) and standard β- elemene (d), showing the match of mass spectra. ............................................................................. 3 Figure S3 Total ion chromatograms of extract of Monomorium chinense workers (a) and standard β- cedrene (b), showing the match of retention times; Mass spectra of peak 3(c) and standard β- cedrene (d), showing the match of mass spectra. .............................................................................. 4 Figure S4 Total ion chromatograms of extract of Monomorium chinense workers (a) and standard (E)-β-farnesene (b), showing the match of retention times; Mass spectra of peak 4(c) and standard (E)-β-farnesene (d), showing the match of mass spectra. -
11.1 IGC Butterflies Compressed Listed by Common Name with Images 7
Indooroopilly Golf Club Natural History - Version 2 Butterflies (Lepidoptera) Listed by Common Name Butterflies and Moths together make up the Order Lepidoptera, one part of the larger group of Insects. Most Butterflies fly during the day and most Moths at night. Observations of Moths have not been made by the authors to date, and this account is limited to the Butterflies. According to the Queensland Museum, there are about 180 species of Butterfly in Southeast Queensland. The 32 species listed here should be viewed as a work-in- progress and many other species are likely to be observed at IGC in the future. These Butterflies are listed below in alphabetical order of Common names. Twenty-six listed species are also illustrated below, approximately in order of Common names. We are very grateful to Mr Jack B Wade (JBW), who has contributed 22 of these images and who has also assisted in their identification. Images Common name Genus species Origin Observations Location on Golf Course DH Blue Tiger Tirumala hamata SEQ native September Red 5 fairway; Green 5 fairway JBW Bright Cornelian Deudorix diovis SEQ native March Male on Blue 3 fairway JBW Cabbage White Pieris rapae SEQ native November various locations JBW Caper Gull Cepora perimale SEQ native March various locations JBW Caper White Belenois java SEQ native November Green 6 fairway JBW Chequered Swallowtail Papilio demoleus SEQ native April, Sep Green 6, on Melaleuca flowers JBW Chrome Awl Hasora chromus SEQ native April near Workshops DH Clearwing Swallowtail Cressida cressida SEQ