LUCI Quarterly Update No 15 January 2019
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© CSIRO 2005 10.1071/IS04020 AC 1445-5226 Invertebrate Systematics, 2005, 19(2), 113–143
© CSIRO 2005 10.1071/IS04020_AC 1445-5226 Invertebrate Systematics, 2005, 19(2), 113–143. When and where did troidine butterflies (Lepidoptera : Papilionidae) evolve? Phylogenetic and biogeographic evidence suggests an origin in remnant Gondwana in the Late Cretaceous Michael F. BrabyA,B,D, John W. H. TruemanA and Rod EastwoodB,C ASchool of Botany and Zoology, The Australian National University, Canberra, ACT 0200, Australia. BMuseum of Comparative Zoology, Harvard University, 26 Oxford St, Cambridge, MA 02138, USA. CAustralian School of Environmental Studies, Griffith University, Nathan, Queensland 4111, Australia. DCorresponding author. Email: [email protected] The age, geographic origin and time of major radiation of the butterflies (Hesperioidea + Papilionoidea + Hedyloidea) are largely unknown. The general modern view is that butterflies arose during the Late Jurassic/Cretaceous in the southern hemisphere (southern Pangea/Gondwana before continental breakup), but this is not universally accepted, and is a best guess based largely on circumstantial evidence. The extreme paucity of fossils and lack of modern, robust, higher-level phylogenies of extant monophyletic groups have been major impediments towards determining reliable estimates of either their age or geographic origin. Here we present a phylogenetic and historical biogeographic analysis of a higher butterfly taxon, the swallowtail tribe Troidini. We analysed molecular data for three protein-encoding genes, mitochondrial ND5 and COI–COII, and nuclear EF–1α, both separately and in combination using maximum parsimony (with and without character weighting and transition/transversion weighting), maximum likelihood and Bayesian methods. Our sample included representatives of all 10 genera of Troidini and distant ingroup taxa (Baroniinae, Parnassiinae, Graphiini, Papilionini), with Pieridae as outgroup. -
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 -
Tera: Papilionidae): Cladistic Reappraisals Using Mainly Immature Stage Characters, with Focus on the Birdwings Ornithoptera Boisduval
Bull. Kitakyushu Mus. Nat. Hist., 15: 43-118. March 28, 1996 Gondwanan Evolution of the Troidine Swallowtails (Lepidop- tera: Papilionidae): Cladistic Reappraisals Using Mainly Immature Stage Characters, with Focus on the Birdwings Ornithoptera Boisduval Michael J. Parsons Entomology Section, Natural History Museum of Los Angeles County 900 Exposition Blvd., LosAngeles, California 90007, U.S.A.*' (Received December 13, 1995) Abstract In order to reappraise the interrelationships of genera in the tribe Troidini, and to test the resultant theory of troidine evolution against biogeographical data a cladistic analysis of troidine genera was performed. Data were obtained mainly from immature stages, providing characters that appeared to be more reliable than many "traditional" adult characters. A single cladogram hypothesising phylogenetic relation ships of the troidine genera was generated. This differs markedly from cladograms obtained in previous studies that used only adult characters. However, the cladogram appears to fit well biogeographical data for the Troidini in terms of vicariance biogcography, especially as this relates to the general hypotheses of Gondwanaland fragmentation and continental drift events advanced by recent geological studies. The genus Ornithoptera is shown to be distinct from Troides. Based on input data drawn equally from immature stages and adult characters, a single cladogram hypothesising the likely phylogeny of Ornithoptera species was generated. With minor weighting of a single important adult character (male -
South East Queensland Big Greasy, Big Attitude
South East Queensland JANUARY 2014 Volume 8 Number 1 Newsletter of the Land for Wildlife Program South East Queensland ISSN 1835-3851 CONTENTS 1 Big Greasy, big attitude 2 Editorial and contacts 3 Fauna Vignettes • There’s a Thingy looking at me! • Nature at Work 4-5 Fauna Profile Cicadas of SEQ 6-7 Flora Profile Aristolochia meridionalis: Hidden Treasure Amongst the Weeds 8 Weed Profile Dutchman’s Pipe: A fatal attractant for butterflies The female Clearwing Swallowtail (top Big Greasy, left) is dingy brown in colour and can fly 9 Fauna Profile long distances, while the male (top right Recovery of the Richmond big attitude and above) is white, black and red and is Birdwing highly territorial. he Big Greasy is one of Australia’s 10-11 My Little Corner Tlargest butterflies whose evolutionary the native and exotic Aristolochias. What is the value of one tree? path can be traced back to when the During spring and summer, the larger Australian, South American and Antarctic male Clearwing Swallowtails (up to 11 Letters to the Editor continents were all joined, making this one 80 mm in size) can be seen flying low, • Nesting in Weeds of the oldest surviving forms of butterfly. patrolling patches of Aristolochia. They • Wild Tobacco - Another View The common name, Big Greasy, I assume, will vigorously defend their patch and comes from the translucent, brown, oust any other butterfly intruder. Smaller 12 Membership Survey Results grease-proof paper looking wings of females will fly long distances in search of the female. The male’s wings are more Aristolochia plants and have reportedly 13 Book Reviews transparent and clear, hence their other travelled 7 kms in one day. -
Donald P.A. Sands · Tim R. New Conservation of the Richmond Birdwing Butter Y in Australia Conservation of the Richmond Birdwing Butterfl Y in Australia
Donald P.A. Sands · Tim R. New Conservation of the Richmond Birdwing Butter y in Australia Conservation of the Richmond Birdwing Butterfl y in Australia (see Fig. 1.10) Donald P.A. Sands • Tim R. New Conservation of the Richmond Birdwing Butterfl y in Australia Donald P.A. Sands Tim R. New Ecosystem Sciences Department of Zoology CSIRO, Brisbane La Trobe University Australia Melbourne Victoria , Australia ISBN 978-94-007-7169-7 ISBN 978-94-007-7170-3 (eBook) DOI 10.1007/978-94-007-7170-3 Springer Dordrecht Heidelberg New York London Library of Congress Control Number: 2013947380 © Springer Science+Business Media Dordrecht 2013 This work is subject to copyright. All rights are reserved by the Publisher, whether the whole or part of the material is concerned, specifi cally the rights of translation, reprinting, reuse of illustrations, recitation, broadcasting, reproduction on microfi lms or in any other physical way, and transmission or information storage and retrieval, electronic adaptation, computer software, or by similar or dissimilar methodology now known or hereafter developed. Exempted from this legal reservation are brief excerpts in connection with reviews or scholarly analysis or material supplied specifi cally for the purpose of being entered and executed on a computer system, for exclusive use by the purchaser of the work. Duplication of this publication or parts thereof is permitted only under the provisions of the Copyright Law of the Publisher’s location, in its current version, and permission for use must always be obtained from Springer. Permissions for use may be obtained through RightsLink at the Copyright Clearance Center. -
44: February, 2012
BUTTERFLY CONSERVATION SA INC. NEWSLETTER No. 44: February, 2012 Below and continued on page 7 is an article by BCSA Chairman, David Keane in the prestigious journal ‘Butterfly’ The magazine of IN THIS ISSUE Butterfly Conservation from the UK • Butterfly Conservation ‘Down Under’ • Public Talks Program 2012 • Book Sale Butterfly Conservation • Lucia limbaria update • Butterfly fact sheets • Bitter-bush Blue fact sheet • Dainty Swallowtail fact sheet DOWN • Bush for Life Workshops • Government House Open Day DavidUNDER Keane explains how he • Friends of Parks AGM established Butterfly Conservation in • New members South Australia. • Diary Dates and notes y interest in butterflies and moths began from my childhood days in southern England. I grew up in Mthe Kent coutnryside near Ashford in the 1950’s. I also attended schools in Devon PUBLIC TALKS PROGRAM and Sussex before emigrating to Australia next talk: 6th March in 1964. Like many children I collected and “From shore to sea; sea shells, sea diplayed the insects I studied. My interest Fiery Jewel Hypochroysope ignita Above: dragons and other amazing sea aligned more to botany as I started to breed Underwing Below: Upper wing. Photos creatures” further details page 2. caterpillars; I had to find what they ate. That RHFisher led me to searching foodplant sites and discovering specific diet requirements. To learn about plants, caterpillars, the adult Lepidoptera and their requirements a whole ecology needed to be understood. On a trip back to my home town in 1997 I met up with members of the Kent Branch of Butterfly Conservation and they took me to various sites. -
Animals Approved for Zoos in New Zealand As of June 2021
INFORMATION SHEET Animals approved for zoos in New Zealand as of June 2021 This is an alphabetical list of animals that can be held in zoos* in New Zealand. Approval numbers that begin with “PRE” were approved prior to July 29 1998 and were subsequently transferred to the HSNO Act. Approval numbers that begin with “NOC” are animal species approved under the HSNO Act after that date. Key to this document: * Approvals may only be used by facilities that are open to the public and approved by the Ministry for Primary Industries for the containment of that species unless the approval code is followed by one of the following symbols: † The approved zoo facility is not required to be open to the public. †† The approval may only be used by the Keystone Wildlife Conservancy containment facility (now known as Gibbs Wildlife Conservancy). ††† Species can also be held under facilities approved to the MAF/ERMA New Zealand Containment Facilities for Vertebrate Laboratory Animals. Species Common name Approval code Abatus shackletoni Koehler, 1911 Sea urchin (echinoids) PRE008972 Acinonyx jubatus Schreber, 1775 Cheetah PRE008902 Acondaster hodgonsoni Yellow starfish PRE008974 Acontaster conspicuous Yellow starfish PRE008973 Acrobates pygmaeus Shaw, 1793 feather tailed glider NOC002541† Adamussium colbecki Smith, 1902 Antarctic scallop (mollusc) PRE008975 Aerothyris fragilis Smith, 1907 brachiopod (mollusc) PRE008976 Aerothyris joubini Blochmann, 1906 brachiopod (mollusc) PRE008977 Ailuropoda melanoleuca David, 1869 giant panda NOC100015† Ailurus fulgens -
259 a Abbott, John, 116, 117 Acanthaceae, 94 Acer Negundo, 14
Index A Amsinckia, 153 Abbott, John, 116, 117 Anaea, 65, 68 Acanthaceae, 94 Anartia amathea, 93, 94 Acer negundo, 14 Anartia fatima, 93–95, 251 Ackery, P. R. (Phil), 19, 21, 25, 33, 144, 218 Anartia jatrophae, 251 Actias luna, 237 Anartia, 65 Actinote, 19 Anatralata versicolor, 156 Adams, Michael, 33, 34 Andrewartha, H. G. (Andy), 249 Adaptation, 80, 157 Animal architecture, 147 Adela flammeusella, 156 Anopina (Tortricidae), 152 Adelpha croaki, 97 Ant, arboreal weaver, 43, 44 Adelpha ixia leucas, 100 Ant-caterpillar interactions, 138, 208 Adelpha messana messana, 100 Anthene emolus, 44, 45 Adelpha phylaca pseudaethalia, 100 Antherosperma moshatum, 123 Adelpha radiata aiellae, 98 Anthocharis cardamines, 226 Adelpha serpa, 97 Anthurium, 17 Adelpha, 97, 100 Ants, vii, 11, 23, 42–45, 68, 121, 134, Adirondack Mountains, 103, 105, 106, 110 137–139, 206, 209, 252 Admiral, Red, 231 Apatelodes paratima, 100 Admiral, Weidemeyer’s, 232 Apatelodidae, 100 Adolfo Lopez Mateos (formerly Chamal), 67 Appalachian Mountains, 105, 116, 126, 161 African mopane worms, 111 Araújo, Aldo, 19, 21 Aglais io, 226 Archonias, 75 Aglais urticae, 226 Arctic, 241, 243–245, 254, 255 Agraulis vanillae, 19 Areniscythris brachypteris (Scythrididae), Aiello, Annette, 137 153, 154, 159 Åland island, 82–86 Argentina, 36–39, 120 Alexander, Martin, 107 Argyrophorus argenteus, 239 Alfalfa butterflies, 62 Argyrotaenia franciscana, 153 Allen, Geoff, 123, 124 Arhopala pseudocentaurus, 44, 45 Allred, Dorald, 153 Aricia, 224 Alpine, Butler’s, 236 Aristolochia longiflora, 62 Alston, Ralph, 66 Aristotelia, 184 Amado, Jorge 143 Arizona State University, 185 Amateur lepidopterists, 7, 8, 184 Armyworm, 1, 108 Amathusiine butterflies, 26 Aroga trialbamaculella, 184 Amazon Forest, 11, 15, 141, 142, 147, 208 Arp, Julius, 206 American Museum of Natural History Arsenura batesii, 98 (AMNH), xi, 28, 241 Arundinaria, 64 Amorim, Felipe, 208 © Springer International Publishing Switzerland 2015 259 L. -
Lepidoptera : Troidini) Avaliadas Através De Modelagem Preditiva De Distribuição De Espécies E Interações Com Suas Plantas Hospedeiras E Biogeografia
GUILHERME WAGNER GUTIERREZ ATENCIO RELAÇÕES ECOLÓGICAS ENTRE EURYADES CORETHRUS BOISDUVAL E EURYADES. DUPONCHELII LUCAS (LEPIDOPTERA : TROIDINI) AVALIADAS ATRAVÉS DE MODELAGEM PREDITIVA DE DISTRIBUIÇÃO DE ESPÉCIES E INTERAÇÕES COM SUAS PLANTAS HOSPEDEIRAS E BIOGEOGRAFIA Dissertação apresentada ao Programa de Pós-Graduação em Biologia Animal, Instituto de Biociências da Universidade Federal do Rio Grande do Sul, como requisito parcial à obtenção do título de Mestre em Biologia Animal. Área de concentração: Biodiversidade Orientador: Prof. Dr. Nicolás Oliveira Mega Universidade Federal do Rio Grande do Sul Porto Alegre, março de 2014. RELAÇÕES ECOLÓGICAS ENTRE EURYADES CORETHRUS BOISDUVAL E EURYADES. DUPONCHELII LUCAS (LEPIDOPTERA: TROIDINI) AVALIADAS ATRAVÉS DE MODELAGEM PREDITIVA DE DISTRIBUIÇÃO DE ESPÉCIES E INTERAÇÕES COM SUAS PLANTAS HOSPEDEIRAS E BIOGEOGRAFIA GUILHERME WAGNER GUTIERREZ ATENCIO Aprovada em _____ de _____________ de 2014. ____________________________________________ Dr. Francisco Cândido Barreto ____________________________________________ Dr. Augusto Ferrari ____________________________________________ Dr. Márcio Borges Martins 2 “From this distant vantage point, the Earth might not seem of any particular interest. But for us, it's different. Consider again that dot. That's here. That's home. That's us. On it, everyone you love, everyone you know, everyone you ever heard of, every human being who ever was, lived out their lives. The aggregate of our joy and suffering, thousands of confident religions, ideologies, and -
Birds, Butterflies and Flowers in the Tropics Are Not More Colourful Than
Global Ecology and Biogeography, (Global Ecol. Biogeogr.) (2015) bs_bs_banner RESEARCH Birds, butterflies and flowers in the PAPERS tropics are not more colourful than those at higher latitudes Rhiannon L. Dalrymple1*, Darrell J. Kemp2,HabacucFlores-Moreno1,3, Shawn W. Laffan4,ThomasE.White2, Frank A. Hemmings5, Marianne L. Tindall1 and Angela T. Moles1 1Evolution and Ecology Research Centre, ABSTRACT School of Biological, Earth and Environmental Aim The idea that species are generally more colourful at tropical latitudes has Sciences, UNSW Australia, Sydney, NSW 2052, Australia, 2Department of Biological held great appeal among biologists since the days of exploration by early naturalists. Sciences, Faculty of Science and Engineering, However, advances in colour quantification and analysis only now allow an objec- Macquarie University, Sydney, NSW 2109, tive test of this idea. We provide the first quantitative analysis of the latitudinal Australia, 3Department of Ecology, Evolution, gradient in colour on a broad scale using data from both animals and plants, and Behavior, University of Minnesota, St encompassing both human-visible and ultraviolet colours. 4 Paul, MN 55108, USA, Centre for Ecosystem Location Australia. Science, School of Biological, Environmental and Earth Sciences, UNSW Australia, Sydney, Methods We collected spectral reflectance data from 570 species or subspecies of NSW 2052, Australia, 5John T. Waterhouse birds, adult forms of 424 species or subspecies of butterflies and the flowers of 339 Herbarium, School of Biological, Earth and species of plants, from latitudes ranging from tropical forests and savannas at Environmental Sciences, UNSW Australia, 9.25° S, to temperate forests and heathlands at 43.75° S. Colour patch saturation, Sydney, NSW 2052, Australia maximum contrast between patches, colour diversity and hue disparity between patches were calculated for all species. -
A Review of the Occurrence and Diversity of the Sphragis in Butterflies
A peer-reviewed open-access journal ZooKeys 694: 41–70 (2017)A review of the occurrence and diversity of the sphragis in butterflies... 41 doi: 10.3897/zookeys.694.13097 REVIEW ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research A review of the occurrence and diversity of the sphragis in butterflies (Lepidoptera, Papilionoidea) Ana Paula S. Carvalho1,2, Albert G. Orr3, Akito Y. Kawahara1,2 1 Entomology and Nematology Department, University of Florida, 1881 Natural Area Dr, Gainesville, FL 32608, United States 2 McGuire Center for Lepidoptera and Biodiversity, Florida Museum of Natural History, University of Florida, 3215 Hull Road, Gainesville, FL, 32611 United States 3 Environmental Futures Rese- arch Institute, Griffith University, Nathan, QLD 4111, Australia Corresponding author: Ana Paula S. Carvalho ([email protected]) Academic editor: T. Simonsen | Received 6 April 2017 | Accepted 7 August 2017 | Published 29 August 2017 http://zoobank.org/6C1FA2F3-C274-4652-A1FA-D5C8570C4ABA Citation: Carvalho APS, Orr AG, Kawahara AY (2017) A review of the occurrence and diversity of the sphragis in butterflies (Lepidoptera, Papilionoidea). ZooKeys 694: 41–70.https://doi.org/10.3897/zookeys.694.13097 Abstract Males of many butterfly species secrete long-lasting mating plugs to prevent their mates from copulating with other males, thus ensuring their sperm will fertilize all future eggs laid. Certain species have fur- ther developed a greatly enlarged, often spectacular, externalized plug, termed a sphragis. This distinctive structure results from complex adaptations in both male and female genitalia and is qualitatively distinct from the amorphous, internal mating plugs of other species. Intermediate conditions between internal plug and external sphragis are rare. -
Phylogenetics and Divergence Times of Papilioninae (Lepidoptera) with Special Reference to the Enigmatic Genera Teinopalpus and Meandrusa
Cladistics Cladistics 27 (2011) 113–137 10.1111/j.1096-0031.2010.00326.x Phylogenetics and divergence times of Papilioninae (Lepidoptera) with special reference to the enigmatic genera Teinopalpus and Meandrusa Thomas J. Simonsena, , Evgeny V. Zakharovb, Marie Djernaesa, Adam M. Cottonc, R.I. Vane-Wrightd and Felix A.H. Sperlinga,* aDepartment of Biological Sciences, University of Alberta, Edmonton, AB, Canada T6G 2E9; bBiodiversity Institute of Ontario, University of Guelph, Guelph, ON, Canada N1G 2W1; c86 ⁄ 2 Moo 5, Tambon Nong Kwai, Hang Dong, Chiang Mai, Thailand 50230; dDurrell Institute of Conservation and Ecology, Department of Anthropology, University of Kent, Canterbury CT2 7NR, UK, and Department of Entomology, Natural History Museum, Cromwell Road, London SW7 5BD, UK Accepted 14 April 2010 Abstract Phylogenetic relationships of 18 genera of the swallowtail subfamily Papilioninae, four genera of Parnassiinae, and the monobasic Baroniinae are inferred based on 94 morphological characters and 5616 bp DNA from seven genes (16S, COI, COII, ND1, ND5, EF-1 alpha and wingless). Bayesian likelihood analyses show that Baroniinae are the sister of a clade comprising Parnassiinae and Papilioninae. Four Papilioninae tribes are recognized, Leptocircini, Teinopalpini, Papilionini and Troidini, with Leptocircini being the sister of the remaining tribes. Meandrusa and Teinopalpus are sister taxa and comprise the tribe Teinopalpini, which is the sister of a clade comprising Papilionini and Troidini. The tribe Troidini (pipevine swallowtails) comprises two subtribes: Battina (including only Battus) and Troidina. The endemic Madagascan genus Pharmacophagus is consistently placed as the sister to the remaining Troidina. The non-Pharmacophagus Troidina are tentatively divided into a Neotropical lineage and an Australasian lineage.