Der Phasmatodea Tree of Life: Überraschendes Und Ungeklärtes in Der Stabschrecken-Evolution
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Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea
Brigham Young University BYU ScholarsArchive Theses and Dissertations 2018-07-01 Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Brigham Young University Follow this and additional works at: https://scholarsarchive.byu.edu/etd Part of the Life Sciences Commons BYU ScholarsArchive Citation Pacheco, Yelena Marlese, "Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea" (2018). Theses and Dissertations. 7444. https://scholarsarchive.byu.edu/etd/7444 This Thesis is brought to you for free and open access by BYU ScholarsArchive. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of BYU ScholarsArchive. For more information, please contact [email protected], [email protected]. Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco A thesis submitted to the faculty of Brigham Young University in partial fulfillment of the requirements for the degree of Master of Science Michael F. Whiting, Chair Sven Bradler Seth M. Bybee Steven D. Leavitt Department of Biology Brigham Young University Copyright © 2018 Yelena Marlese Pacheco All Rights Reserved ABSTRACT Ecomorph Convergence in Stick Insects (Phasmatodea) with Emphasis on the Lonchodinae of Papua New Guinea Yelena Marlese Pacheco Department of Biology, BYU Master of Science Phasmatodea exhibit a variety of cryptic ecomorphs associated with various microhabitats. Multiple ecomorphs are present in the stick insect fauna from Papua New Guinea, including the tree lobster, spiny, and long slender forms. While ecomorphs have long been recognized in phasmids, there has yet to be an attempt to objectively define and study the evolution of these ecomorphs. -
Metabolic Rate Depression Is Induced by Caloric Restriction and Correlates with Rate of Development and Lifespan in a Parthenogenetic Insect
Experimental Gerontology 44 (2009) 413–419 Contents lists available at ScienceDirect Experimental Gerontology journal homepage: www.elsevier.com/locate/expgero Metabolic rate depression is induced by caloric restriction and correlates with rate of development and lifespan in a parthenogenetic insect Alison M. Roark *, Karen A. Bjorndal Department of Zoology, University of Florida, Box 118525, Gainesville, FL 32611-8525, USA article info abstract Article history: Caloric restriction (CR) extends lifespan in most animals, but the mechanisms underlying this phenom- Received 8 January 2009 enon are the subject of much debate. We investigated the association between longevity and resting met- Received in revised form 10 March 2009 abolic rate (RMR) in Indian stick insects (Carausius morosus) by (i) determining the appropriate scaling Accepted 17 March 2009 coefficient for calculating mass-corrected RMR of insects throughout development, (ii) quantifying the Available online 26 March 2009 response of RMR to diet history, and (iii) correlating RMR in multiple life-history stages with adult and total lifespan. Over a range of body sizes, whole-body RMR (measured as oxygen consumption rate) Keywords: scaled linearly with body mass. Mass-specific RMR decreased in response to CR, particularly when food Ad libitum was restricted during juvenile stages. With one exception, RMR of insects in different life-history stages Body size Carausius morosus matched current feeding level and was not substantially affected by intake history. Total lifespan was Dietary restriction affected by intake, with insects that experienced CR early in development living longer than insects that Food restriction were fed ad libitum. Although CR was associated with extended total lifespan and decreased RMR, it was Longevity also associated with shortened adult lifespan. -
Insecta: Phasmatodea) and Their Phylogeny
insects Article Three Complete Mitochondrial Genomes of Orestes guangxiensis, Peruphasma schultei, and Phryganistria guangxiensis (Insecta: Phasmatodea) and Their Phylogeny Ke-Ke Xu 1, Qing-Ping Chen 1, Sam Pedro Galilee Ayivi 1 , Jia-Yin Guan 1, Kenneth B. Storey 2, Dan-Na Yu 1,3 and Jia-Yong Zhang 1,3,* 1 College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China; [email protected] (K.-K.X.); [email protected] (Q.-P.C.); [email protected] (S.P.G.A.); [email protected] (J.-Y.G.); [email protected] (D.-N.Y.) 2 Department of Biology, Carleton University, Ottawa, ON K1S 5B6, Canada; [email protected] 3 Key Lab of Wildlife Biotechnology, Conservation and Utilization of Zhejiang Province, Zhejiang Normal University, Jinhua 321004, China * Correspondence: [email protected] or [email protected] Simple Summary: Twenty-seven complete mitochondrial genomes of Phasmatodea have been published in the NCBI. To shed light on the intra-ordinal and inter-ordinal relationships among Phas- matodea, more mitochondrial genomes of stick insects are used to explore mitogenome structures and clarify the disputes regarding the phylogenetic relationships among Phasmatodea. We sequence and annotate the first acquired complete mitochondrial genome from the family Pseudophasmati- dae (Peruphasma schultei), the first reported mitochondrial genome from the genus Phryganistria Citation: Xu, K.-K.; Chen, Q.-P.; Ayivi, of Phasmatidae (P. guangxiensis), and the complete mitochondrial genome of Orestes guangxiensis S.P.G.; Guan, J.-Y.; Storey, K.B.; Yu, belonging to the family Heteropterygidae. We analyze the gene composition and the structure D.-N.; Zhang, J.-Y. -
Insects, Beetles, Bugs and Slugs of Mt Gravatt Conservation Reserve
Insects, beetles, bugs and slugs of Mt Gravatt Conservation Reserve Compiled by: Michael Fox www.megoutlook.org/flora-fauna/ © 2015-20 Creative Commons – free use with attribution to Mt Gravatt Environment Group Ants Dolichoderinae Iridomyrmex sp. Small Meat Ant Attendant “Kropotkin” ants with caterpillar of Imperial Hairstreak butterfly. Ants provide protection in return for sugary fluids secreted by the caterpillar. Note the strong jaws. These ants don’t sting but can give a powerful bite. Kropotkin is a reference to Russian biologist Peter Kropotkin who proposed a concept of evolution based on “mutual aid” helping species from ants to higher mammals survive. 4-Nov-20 Insects Beetles and Bugs - ver 5.9.docx Page 1 of 59 Mt Gravatt Environment Group – www.megoutlook.wordpress.com Insects, beetles, bugs and slugs of Mt Gravatt Conservation Reserve Formicinae Opisthopsis rufithorax Black-headed Strobe Ant Formicinae Camponotus consobrinus Banded Sugar Ant Size 10mm Eggs in rotting log 4-Nov-20 Insects Beetles and Bugs - ver 5.9.docx Page 2 of 59 Mt Gravatt Environment Group – www.megoutlook.wordpress.com Insects, beetles, bugs and slugs of Mt Gravatt Conservation Reserve Formicinae Camponotus nigriceps Black-headed Sugar Ant 4-Nov-20 Insects Beetles and Bugs - ver 5.9.docx Page 3 of 59 Mt Gravatt Environment Group – www.megoutlook.wordpress.com Insects, beetles, bugs and slugs of Mt Gravatt Conservation Reserve Formicinae Polyrhachis ammon Golden-tailed Spiny Ant Large spines at rear of thorax Nest 4-Nov-20 Insects Beetles and Bugs - ver 5.9.docx Page 4 of 59 Mt Gravatt Environment Group – www.megoutlook.wordpress.com Insects, beetles, bugs and slugs of Mt Gravatt Conservation Reserve Formicinae Polyrhachis australis Rattle Ant Black Weaver Ant or Dome-backed Spiny Ant Feeding on sugar secretions produced by Redgum Lerp Psyllid. -
(Phasmida: Diapheromeridae) from Colombia
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 11-27-2020 A new species of Oncotophasma Rehn, 1904 (Phasmida: Diapheromeridae) from Colombia Andres David Murcia Oscar J. Cadena-Castañeda Daniela Santos Martins Silva Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons This Article is brought to you for free and open access by the Center for Systematic Entomology, Gainesville, Florida at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Insecta Mundi by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. A journal of world insect systematics INSECTA MUNDI 0819 A new species of Oncotophasma Rehn, 1904 Page Count: 7 (Phasmida: Diapheromeridae) from Colombia Andres David Murcia Universidad Distrital Francisco José de Caldas. Grupo de Investigación en Artrópodos “Kumangui” Carrera 3 # 26A – 40 Bogotá, DC, Colombia Oscar J. Cadena-Castañeda Universidad Distrital Francisco José de Caldas Grupo de Investigación en Artrópodos “Kumangui” Carrera 3 # 26A – 40 Bogotá, DC, Colombia Daniela Santos Martins Silva Universidade Federal de Viçosa (UFV) campus Rio Paranaíba, Instituto de Ciências Biológicas e da Saúde Rodovia MG 230, KM 7, 38810–000 Rio Paranaíba, MG, Brazil Date of issue: November 27, 2020 Center for Systematic Entomology, Inc., Gainesville, FL Murcia AD, Cadena-Castañeda OJ, Silva DSM. 2020. A new species of Oncotophasma Rehn, 1904 (Phasmida: Diapheromeridae) from Colombia. Insecta Mundi 0819: 1–7. Published on November 27, 2020 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. -
Phasmida (Stick and Leaf Insects)
● Phasmida (Stick and leaf insects) Class Insecta Order Phasmida Number of families 8 Photo: A leaf insect (Phyllium bioculatum) in Japan. (Photo by ©Ron Austing/Photo Researchers, Inc. Reproduced by permission.) Evolution and systematics Anareolatae. The Timematodea has only one family, the The oldest fossil specimens of Phasmida date to the Tri- Timematidae (1 genus, 21 species). These small stick insects assic period—as long ago as 225 million years. Relatively few are not typical phasmids, having the ability to jump, unlike fossil species have been found, and they include doubtful almost all other species in the order. It is questionable whether records. Occasionally a puzzle to entomologists, the Phasmida they are indeed phasmids, and phylogenetic research is not (whose name derives from a Greek word meaning “appari- conclusive. Studies relating to phylogeny are scarce and lim- tion”) comprise stick and leaf insects, generally accepted as ited in scope. The eggs of each phasmid are distinctive and orthopteroid insects. Other alternatives have been proposed, are important in classification of these insects. however. There are about 3,000 species of phasmids, although in this understudied order this number probably includes about 30% as yet unidentified synonyms (repeated descrip- Physical characteristics tions). Numerous species still await formal description. Stick insects range in length from Timema cristinae at 0.46 in (11.6 mm) to Phobaeticus kirbyi at 12.9 in (328 mm), or 21.5 Extant species usually are divided into eight families, in (546 mm) with legs outstretched. Numerous phasmid “gi- though some researchers cite just two, based on a reluctance ants” easily rank as the world’s longest insects. -
Insect Conservation and Islands Insect Conservation and Islands
INSECT CONSERVATION AND ISLANDS INSECT CONSERVATION AND ISLANDS Editor T. R. New La Trobe University, Melbourne, Australia Reprinted from Journal of Insect Conservation Volume 12, Numbers 3–4 (2008) 123 A C.I.P. Catalogue record for this book is available from the library of Congress. ISBN-13 978-1-4020-8781-3 (HB) ISBN-13 978-1-4020-8782-0 (e-book) Published by Springer P.O. Box 17, 3300 AA Dordrecht, The Netherlands www.springer.com Cover illustration: The cover illustration shows several examples of spectacular weta (Orthoptera) from New Zealand, where their conservation has depended largely on offshore islands as refuges and introduction sites, as discussed in papers in this publication. The insects can be fitted with harmonic radar transponders or micro- transmitters for individual tracking. Shown are a Cook Strait Giant Weta, and two Mercury Island Tusked Weta (photograph courtesy of Danny Thornburrow, Corinne Watts and Ian Stringer). Printed on acid-free paper All Rights Reserved Ó 2008 Springer No part of the material protected by this copyright notice may be reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording or by any information storage and retrieval system, without written permission from the copyright owner. Table of Contents EDITORIAL A special issue on insect conservation and islands T.R. New 1 PAPERS Insect conservation on islands: setting the scene and defining the needs T.R. New 3–10 Butterflies of European islands: the implications of the geography and ecology of rarity and endemicity for conservation R.L.H. Dennis · L. -
Phasmatodea, Diapheromeridae, Diapheromerinae)
Bulletin de la Société entomologique de France, 121 (2), 2016 : 141-148. A new stick insect of the genus Oncotophasma from Costa Rica (Phasmatodea, Diapheromeridae, Diapheromerinae) by Yannick BELLANGER La Ville Jouy, F – 22250 Trédias <[email protected]> http://zoobank.org/66A4E377-E7F3-4684-9708-CDEBAB68622A Abstract. – A new species of Phasmatodea, Oncotophasma laetitiae n. sp. from Costa Rica, is described and illustrated in both sexes and the egg. Résumé. – Un nouveau Phasme du genre Oncotophasma du Costa Rica (Phasmatodea, Diapheromeridae, Diapheromerinae). Une nouvelle espèce de Phasmatodea du Costa Rica, Oncotophasma laetitiae n. sp., est décrite et illustrée, incluant les deux sexes et l’œuf. Resumen. – Un nuevo fásmido del género Oncotophasma de Costa-Rica (Phasmatodea, Diapheromeridae, Diaphero merinae). Una nueva especie de Phasmatodea de Costa Rica, Oncotophasma laetitiae n. sp., es descrita e ilustrada, incluyendo ambos sexos y el huevo. Keywords. – New species, taxonomy, morphology, host plant. _________________ A new phasmid species was collected by the author in 2011 in Costa Rica, in the Heredia Province at the Research Station of Refugio de Vida Silvestre Cerro Dantas, at about 2000 m above sea level. Three females, one male and two female nymphs were found on the same shrub but only one pair was collected. The specimens were found in copula, which confirms them to be conspecific. The author obtained one egg from the female kept alive an extra night. Examination has shown this species to belong in the genus Oncotophasma Rehn, 1904 (Diapheromerinae, Diapheromerini) and detailed comparison with the types of the known species has proven this to be a still undescribed species. -
Phasmid Studies ISSN 0966-0011 Volume 9, Numbers 1 & 2
Phasmid Studies ISSN 0966-0011 volume 9, numbers 1 & 2. Contents Species Report PSG. 122, Anisomorpha monstrosa Hebard Paul A. Hoskisson . 1 Cigarrophasma, a new genus of stick-insect (Phasmatidae) from Australia Paul D. Brock & Jack Hasenpusch . 0 •••••• 0 ••• 0 ••••••• 4 A review of the genus Medaura Stal, 1875 (Phasmatidae: Phasmatinae), including the description of a new species from Bangladesh Paul Do Brock & Nicolas Cliquennois 11 First records and discovery of two new species of Anisomorpha Gray (Phasmida: Pseudophasmatidae) in Haiti and Dominican Republic Daniel E. Perez-Gelabert 0 .. .. 0 • • • • • • 0 • • • • 0 • • 0 • 0 • • 0 0 • • • 27 Species report on Pharnacia biceps Redtenbacher, PSG 203 Wim Potvin 0 ••• 28 How Anisomorpha got its stripes? Paul Hoskisson . 33 Reviews and Abstracts Book Reviews . 35 Phasmid Abstracts 38 Cover illustr ation : Orthonecroscia pulcherrima Kirby, drawing by PoE. Bragg. Species Report PSG. 122, Anisomorpha monstrosa Hebard Paul A. Hoskisson, School of Biomolecular Sciences, Liverpool John Moores University, Byrom Street, Liverpool, 13 3AF, UK. With illustrations by P.E. Bragg. Abstract This report summarises the care and breeding of Anisomorpha monstrosa Hebard, the largest species in the genus. Behaviour and defence mechanism are also discussed along with descriptions of the eggs, nymphs, and adults. Key words Phasmida, Anisomorpha monstrosa, Pseudophasmatinae, Rearing, Distribution, Defence. Taxonomy Anisomorpha monstrosa belongs to the sub-family Pseudophasmatinae. It was described in 1932 by Hebard (1932: 214) and is the largest species in the genus. The type specimen is a female collected from Merida, in Yucatan, Mexico. Culture History The original culture of this species was collected in Belize, approximately 150km north of Belize City by Jan Meerman in 1993 or 1994 (D'Hulster, personal communication). -
ARTHROPODA Subphylum Hexapoda Protura, Springtails, Diplura, and Insects
NINE Phylum ARTHROPODA SUBPHYLUM HEXAPODA Protura, springtails, Diplura, and insects ROD P. MACFARLANE, PETER A. MADDISON, IAN G. ANDREW, JOCELYN A. BERRY, PETER M. JOHNS, ROBERT J. B. HOARE, MARIE-CLAUDE LARIVIÈRE, PENELOPE GREENSLADE, ROSA C. HENDERSON, COURTenaY N. SMITHERS, RicarDO L. PALMA, JOHN B. WARD, ROBERT L. C. PILGRIM, DaVID R. TOWNS, IAN McLELLAN, DAVID A. J. TEULON, TERRY R. HITCHINGS, VICTOR F. EASTOP, NICHOLAS A. MARTIN, MURRAY J. FLETCHER, MARLON A. W. STUFKENS, PAMELA J. DALE, Daniel BURCKHARDT, THOMAS R. BUCKLEY, STEVEN A. TREWICK defining feature of the Hexapoda, as the name suggests, is six legs. Also, the body comprises a head, thorax, and abdomen. The number A of abdominal segments varies, however; there are only six in the Collembola (springtails), 9–12 in the Protura, and 10 in the Diplura, whereas in all other hexapods there are strictly 11. Insects are now regarded as comprising only those hexapods with 11 abdominal segments. Whereas crustaceans are the dominant group of arthropods in the sea, hexapods prevail on land, in numbers and biomass. Altogether, the Hexapoda constitutes the most diverse group of animals – the estimated number of described species worldwide is just over 900,000, with the beetles (order Coleoptera) comprising more than a third of these. Today, the Hexapoda is considered to contain four classes – the Insecta, and the Protura, Collembola, and Diplura. The latter three classes were formerly allied with the insect orders Archaeognatha (jumping bristletails) and Thysanura (silverfish) as the insect subclass Apterygota (‘wingless’). The Apterygota is now regarded as an artificial assemblage (Bitsch & Bitsch 2000). -
Synopsis of the Hymenopteran Fauna of Lord Howe Island with a Preliminary Checklist of Species
Zootaxa 3931 (3): 423–432 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2015 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3931.3.6 http://zoobank.org/urn:lsid:zoobank.org:pub:4FA7FEAD-1622-413C-8251-B7470405D7B7 Synopsis of the hymenopteran fauna of Lord Howe Island with a preliminary checklist of species JOHN T. JENNINGS & ANDREW D. AUSTIN Australian Centre for Evolutionary Biology and Biodiversity, and School of Biological Sciences, The University of Adelaide, SA 5005, Australia. E-mail: [email protected] or [email protected] Abstract Lord Howe Island is an eroded remnant of a shield volcano approximately 600 km northeast of Sydney, New South Wales, Australia. It has fascinated biologists for more than a century because of its unique and iconic fauna and flora, and was declared a World Heritage Site in 1982. Although the terrestrial invertebrate fauna is reasonably well known for many groups, most Hymenoptera, apart from ants, have received scant attention. Here we use material collected from a recent intensive invertebrate survey, in conjunction with the published literature, to provide an overview of the Hymenoptera known from the island that can act as a basis for future taxonomic and biodiversity research. In doing so, we record 318 species from 31 hymenopteran families from the Island, and assess the proportion that are flightless and likely to be en- demic to the island. Key words: oceanic island, endemic species, apterous, brachypterous Introduction Lord Howe Island, a World Heritage Site of global significance since 1982, is located approximately 600 km northeast of Sydney, New South Wales (Fig. -
Spineless Spineless Rachael Kemp and Jonathan E
Spineless Status and trends of the world’s invertebrates Edited by Ben Collen, Monika Böhm, Rachael Kemp and Jonathan E. M. Baillie Spineless Spineless Status and trends of the world’s invertebrates of the world’s Status and trends Spineless Status and trends of the world’s invertebrates Edited by Ben Collen, Monika Böhm, Rachael Kemp and Jonathan E. M. Baillie Disclaimer The designation of the geographic entities in this report, and the presentation of the material, do not imply the expressions of any opinion on the part of ZSL, IUCN or Wildscreen concerning the legal status of any country, territory, area, or its authorities, or concerning the delimitation of its frontiers or boundaries. Citation Collen B, Böhm M, Kemp R & Baillie JEM (2012) Spineless: status and trends of the world’s invertebrates. Zoological Society of London, United Kingdom ISBN 978-0-900881-68-8 Spineless: status and trends of the world’s invertebrates (paperback) 978-0-900881-70-1 Spineless: status and trends of the world’s invertebrates (online version) Editors Ben Collen, Monika Böhm, Rachael Kemp and Jonathan E. M. Baillie Zoological Society of London Founded in 1826, the Zoological Society of London (ZSL) is an international scientifi c, conservation and educational charity: our key role is the conservation of animals and their habitats. www.zsl.org International Union for Conservation of Nature International Union for Conservation of Nature (IUCN) helps the world fi nd pragmatic solutions to our most pressing environment and development challenges. www.iucn.org Wildscreen Wildscreen is a UK-based charity, whose mission is to use the power of wildlife imagery to inspire the global community to discover, value and protect the natural world.