Zootaxa, Annotated Checklist of Weevils from the Papuan Region

Total Page:16

File Type:pdf, Size:1020Kb

Zootaxa, Annotated Checklist of Weevils from the Papuan Region ZOOTAXA 1536 Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) GREGORY P. SETLIFF Magnolia Press Auckland, New Zealand Zootaxa 1536 © 2007 Magnolia Press · 1 Gregory P. Setliff Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) (Zootaxa 1536) 296 pp.; 30 cm. 30 July 2007 ISBN 978-1-86977-139-3 (paperback) ISBN 978-1-86977-140-9 (Online edition) FIRST PUBLISHED IN 2007 BY Magnolia Press P.O. Box 41-383 Auckland 1346 New Zealand e-mail: [email protected] http://www.mapress.com/zootaxa/ © 2007 Magnolia Press All rights reserved. No part of this publication may be reproduced, stored, transmitted or disseminated, in any form, or by any means, without prior written permission from the publisher, to whom all requests to reproduce copyright material should be directed in writing. This authorization does not extend to any other kind of copying, by any means, in any form, and for any purpose other than private research use. ISSN 1175-5326 (Print edition) ISSN 1175-5334 (Online edition) 2 · Zootaxa 1536 © 2007 Magnolia Press SETLIFF Zootaxa 1536: 1–296 (2007) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2007 · Magnolia Press ISSN 1175-5334 (online edition) Annotated checklist of weevils from the Papuan region (Coleoptera, Curculionoidea) GREGORY P. SETLIFF Department of Entomology, University of Minnesota, 219 Hodson, 1980 Folwell Avenue, St. Paul, Minnesota 55108 U.S.A. & The New Guinea Binatang Research Center, P. O. Box 604, Madang, Papua New Guinea. Email: [email protected] Table of contents ABSTRACT ........................................................................................................................................................................4 INTRODUCTION ...............................................................................................................................................................4 Historical Papuan collections.............................................................................................................................................. 5 Taxonomic history: specialists ............................................................................................................................................5 Taxonomic history: catalogs and checklists ........................................................................................................................7 METHODS AND CONVENTIONS EMPLOYED ............................................................................................................7 Faunal area and gazetteer ....................................................................................................................................................7 Classification followed........................................................................................................................................................ 8 Format of checklist entries ..................................................................................................................................................9 Compilation of the bibliography .........................................................................................................................................9 NOMENCLATURAL CHANGES .....................................................................................................................................9 New type-species designations ........................................................................................................................................... 9 New synonymies ...............................................................................................................................................................11 Changes in status ...............................................................................................................................................................11 New combinations .............................................................................................................................................................12 PROBLEMATIC RECORDS ............................................................................................................................................14 INTRODUCED SPECIES ................................................................................................................................................16 Biological control agents ...................................................................................................................................................16 Pollinator species ..............................................................................................................................................................16 ACKNOWLEDGMENTS .................................................................................................................................................16 SYNOPSIS OF FAMILY-LEVEL CLASSIFICATION ....................................................................................................17 CHECKLIST .....................................................................................................................................................................19 Nemonychidae ...................................................................................................................................................................19 Anthribidae ........................................................................................................................................................................19 Belidae ...............................................................................................................................................................................43 Rhynchitidae .....................................................................................................................................................................43 Attelabidae ........................................................................................................................................................................ 45 Brentidae ...........................................................................................................................................................................51 Apionidae ..........................................................................................................................................................................68 Brachyceridae ....................................................................................................................................................................72 Dryophthoridae ................................................................................................................................................................. 72 Erirhinidae .........................................................................................................................................................................80 Curculionidae ....................................................................................................................................................................80 REFERENCES ................................................................................................................................................................220 INDEX .............................................................................................................................................................................248 Accepted by Q. Wang: 3 Mar. 2007; published: 30 Jul. 2007 3 APPENDIX 1. .................................................................................................................................................................282 APPENDIX 2. .................................................................................................................................................................286 APPENDIX 3. .................................................................................................................................................................297 ABSTRACT The following checklist includes 2,955 species-group names and 553 genus-group names of weevils occurring in the Papuan region. Major islands treated are: Aru, Biak, Bougainville, Manus, Mysol, New Guinea, Salawatti, Trobriand, Waigeo, Woodlark, and Yapen Islands and the islands of the Admiralty, Bismarck, d’Entrecasteaux, and Louisaide Archi- pelagoes. Maps of the region with historically important collection localities are provided. Entomological expeditions to the region and collections containing significant weevil material are summarized. All available family-group, genus- group and species-group names are arranged alphabetically for all families of Curculionoidea known from the region. All currently accepted species epithet are annotated with taxonomic references, notes on published distributions, past taxo- nomic changes, infrasubspecific names, and species-group synonymies. The following nomenclatural changes are pro- posed: the monotypic genus Neplaxa Casey is a new synonym of Pantoxystus Pascoe; its type species Neplaxa illustratus Casey is a new synonym of Pantoxystus rubricollis (Boisduval). Two subgenera of Neosynaptops, Neosynap- topsis Legalov and Pseudosynaptos Legalov are new synonymies of Euops (Neosynaptops) Voss revised status. Type- species are designated
Recommended publications
  • Green-Tree Retention and Controlled Burning in Restoration and Conservation of Beetle Diversity in Boreal Forests
    Dissertationes Forestales 21 Green-tree retention and controlled burning in restoration and conservation of beetle diversity in boreal forests Esko Hyvärinen Faculty of Forestry University of Joensuu Academic dissertation To be presented, with the permission of the Faculty of Forestry of the University of Joensuu, for public criticism in auditorium C2 of the University of Joensuu, Yliopistonkatu 4, Joensuu, on 9th June 2006, at 12 o’clock noon. 2 Title: Green-tree retention and controlled burning in restoration and conservation of beetle diversity in boreal forests Author: Esko Hyvärinen Dissertationes Forestales 21 Supervisors: Prof. Jari Kouki, Faculty of Forestry, University of Joensuu, Finland Docent Petri Martikainen, Faculty of Forestry, University of Joensuu, Finland Pre-examiners: Docent Jyrki Muona, Finnish Museum of Natural History, Zoological Museum, University of Helsinki, Helsinki, Finland Docent Tomas Roslin, Department of Biological and Environmental Sciences, Division of Population Biology, University of Helsinki, Helsinki, Finland Opponent: Prof. Bengt Gunnar Jonsson, Department of Natural Sciences, Mid Sweden University, Sundsvall, Sweden ISSN 1795-7389 ISBN-13: 978-951-651-130-9 (PDF) ISBN-10: 951-651-130-9 (PDF) Paper copy printed: Joensuun yliopistopaino, 2006 Publishers: The Finnish Society of Forest Science Finnish Forest Research Institute Faculty of Agriculture and Forestry of the University of Helsinki Faculty of Forestry of the University of Joensuu Editorial Office: The Finnish Society of Forest Science Unioninkatu 40A, 00170 Helsinki, Finland http://www.metla.fi/dissertationes 3 Hyvärinen, Esko 2006. Green-tree retention and controlled burning in restoration and conservation of beetle diversity in boreal forests. University of Joensuu, Faculty of Forestry. ABSTRACT The main aim of this thesis was to demonstrate the effects of green-tree retention and controlled burning on beetles (Coleoptera) in order to provide information applicable to the restoration and conservation of beetle species diversity in boreal forests.
    [Show full text]
  • Lista De Especies De Curculionoidea Depositadas En La Colecci.N De
    Acta Zool. Mex. (n.s.) 87: 147-165 (2002) LISTA DE LAS ESPECIES DE CURCULIONOIDEA (INSECTA: COLEOPTERA) DEPOSITADAS EN LA COLECCIÓN DEL MUSEO DE ZOOLOGÍA "ALFONSO L. HERRERA", FACULTAD DE CIENCIAS, UNAM (MZFC) Juan J. MORRONE1, Raúl MUÑIZ2, Julieta ASIAIN3 y Juan MÁRQUEZ1,3 1 Museo de Zoología, Departamento de Biología Evolutiva, Facultad de Ciencias, UNAM, Apdo. postal 70-399, CP 04510 México D.F., MÉXICO 2 Lago Cuitzeo # 144, CP 11320. México, D. F. MÉXICO 3 Laboratorio Especializado de Morfofisiología Animal, Facultad de Ciencias, UNAM, Apdo. postal 70-399, CP 04510 México D.F., MÉXICO RESUMEN La colección del Museo de Zoología "Alfonso L. Herrera" incluye 1,148 especímenes de Curculionoidea, que pertenecen a 397 especies, 217 géneros y 14 familias. La familia mejor representada es Curculionidae, con 342 especies, seguida de Dryophthoridae (12), Erirhinidae (8), Belidae (7), Oxycorynidae (6), Brentidae (4), Nemonychidae (4), Rhynchitidae (4), Anthribidae (3), Apionidae (2), Brachyceridae (2), Attelabidae (1), Ithyceridae (1) y Raymondionymidae (1). Muchos de los especímenes provienen de otros países (Argentina, Chile, Brasil y E.U.A., entre otros). La mayoría de los ejemplares mexicanos son de los estados de Hidalgo (44 especies), Morelos (13), Nayarit (12) y Veracruz (12). Palabras Clave: Coleoptera, Curculionoidea, Curculionidae, colección. ABSTRACT The collection of the Museo de Zoología "Alfonso L. Herrera" includes 1,148 specimens of Curculionoidea, which belong to 397 species, 217 genera, and 14 families. The best represented family is Curculionidae, with 342 species, followed by Dryophthoridae (12), Erirhinidae (8), Belidae (7), Oxycorynidae (6), Brentidae (4), Nemonychidae (4), Rhynchitidae (4), Anthribidae (3), Apionidae (2), Brachyceridae (2), Attelabidae (1), Ithyceridae (1), and Raymondionymidae (1).
    [Show full text]
  • The Curculionoidea of the Maltese Islands (Central Mediterranean) (Coleoptera)
    BULLETIN OF THE ENTOMOLOGICAL SOCIETY OF MALTA (2010) Vol. 3 : 55-143 The Curculionoidea of the Maltese Islands (Central Mediterranean) (Coleoptera) David MIFSUD1 & Enzo COLONNELLI2 ABSTRACT. The Curculionoidea of the families Anthribidae, Rhynchitidae, Apionidae, Nanophyidae, Brachyceridae, Curculionidae, Erirhinidae, Raymondionymidae, Dryophthoridae and Scolytidae from the Maltese islands are reviewed. A total of 182 species are included, of which the following 51 species represent new records for this archipelago: Araecerus fasciculatus and Noxius curtirostris in Anthribidae; Protapion interjectum and Taeniapion rufulum in Apionidae; Corimalia centromaculata and C. tamarisci in Nanophyidae; Amaurorhinus bewickianus, A. sp. nr. paganettii, Brachypera fallax, B. lunata, B. zoilus, Ceutorhynchus leprieuri, Charagmus gressorius, Coniatus tamarisci, Coniocleonus pseudobliquus, Conorhynchus brevirostris, Cosmobaris alboseriata, C. scolopacea, Derelomus chamaeropis, Echinodera sp. nr. variegata, Hypera sp. nr. tenuirostris, Hypurus bertrandi, Larinus scolymi, Leptolepurus meridionalis, Limobius mixtus, Lixus brevirostris, L. punctiventris, L. vilis, Naupactus cervinus, Otiorhynchus armatus, O. liguricus, Rhamphus oxyacanthae, Rhinusa antirrhini, R. herbarum, R. moroderi, Sharpia rubida, Sibinia femoralis, Smicronyx albosquamosus, S. brevicornis, S. rufipennis, Stenocarus ruficornis, Styphloderes exsculptus, Trichosirocalus centrimacula, Tychius argentatus, T. bicolor, T. pauperculus and T. pusillus in Curculionidae; Sitophilus zeamais and
    [Show full text]
  • FIRST REPORT of a SNOUT WEEVIL Alcidodes Sp
    FIRST REPORT OF A SNOUT WEEVIL Alcidodes sp. (COLEOPTERA: CURCULIONIDAE) FIELD INFESTATION ON MANGO Mangifera indica L. (ANACARDIACEAE) IN PERLIS, MALAYSIA Nurul Huda, A.1, 2*, Che Salmah, M.R.2, Hamdan, A.2 & Abdul Razak, M.N.3 1 Department of Plant Science, Kulliyyah of Science, International Islamic University Malaysia, 25200 Kuantan, Pahang, Malaysia. 2School of Biological Sciences, Universiti Sains Malaysia, 11800 Penang, Malaysia 3Faculty of Plantation and Agro-technology, Universiti Teknologi MARA, 02600 Arau, Perlis, Malaysia *Corresponding email: [email protected] ABSTRACT An infestation of a snout weevil Alcidodes sp. (Coleoptera: Curculionidae) on Mangifera indica L. (Anacardiaceae) was scientifically reported for the first time in Malaysia. This snout weevil causes severe damage on young stems and flower panicles. Even though the tree survived from a few infestations, but severe cases could pose a serious economic implication on the productivity of the crop. Thus more research regarding the pest management of M. indica is required to maximize mango production in Malaysia. Keywords: Alcidodes, Curculionidae, mango, pest ABSTRAK Penularan kumbang muncung panjang Alcidodes sp. (Coleoptera: Curculionidae) pada Mangifera indica L. (Anacardiaceae) dilaporkan secara saintifik buat kali pertama di Malaysia. Kumbang muncung panjang ini menyebabkan kerosakan teruk pada batang muda and tangkai bunga. Walaupun pokok tersebut terselamat daripada beberapa serangan tetapi kes-kes yang teruk boleh menimbulkan implikasi ekonomi yang serius terhadap produktiviti tanaman. Oleh itu lebih banyak kajian mengenai pengurusan perosak M. indica diperlukan untuk memaksimumkan pengeluaran mangga di Malaysia. Kata kunci: Alcidodes, Curculionidae, mangga, perosak INTRODUCTION The largest number of Mangifera species originate in Tropical Asia (Bally 2006) and occur in the Malay Peninsula, the Indonesian archipelago, Thailand, Indochina and the Philippines (Mukherjee 1972; Mukherjee & Litz 2009).
    [Show full text]
  • (Coleoptera) from European Eocene Ambers
    geosciences Review A Review of the Curculionoidea (Coleoptera) from European Eocene Ambers Andrei A. Legalov 1,2 1 Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences, Frunze Street 11, 630091 Novosibirsk, Russia; [email protected]; Tel.: +7-9139471413 2 Biological Institute, Tomsk State University, Lenina Prospekt 36, 634050 Tomsk, Russia Received: 16 October 2019; Accepted: 23 December 2019; Published: 30 December 2019 Abstract: All 142 known species of Curculionoidea in Eocene amber are documented, including one species of Nemonychidae, 16 species of Anthribidae, six species of Belidae, 10 species of Rhynchitidae, 13 species of Brentidae, 70 species of Curcuionidae, two species of Platypodidae, and 24 species of Scolytidae. Oise amber has eight species, Baltic amber has 118 species, and Rovno amber has 16 species. Nine new genera and 18 new species are described from Baltic amber. Four new synonyms are noted: Palaeometrioxena Legalov, 2012, syn. nov. is synonymous with Archimetrioxena Voss, 1953; Paleopissodes weigangae Ulke, 1947, syn. nov. is synonymous with Electrotribus theryi Hustache, 1942; Electrotribus erectosquamata Rheinheimer, 2007, syn. nov. is synonymous with Succinostyphlus mroczkowskii Kuska, 1996; Protonaupactus Zherikhin, 1971, syn. nov. is synonymous with Paonaupactus Voss, 1953. Keys for Eocene amber Curculionoidea are given. There are the first records of Aedemonini and Camarotini, and genera Limalophus and Cenocephalus in Baltic amber. Keywords: Coleoptera; Curculionoidea; fossil weevil; new taxa; keys; Palaeogene 1. Introduction The Curculionoidea are one of the largest and most diverse groups of beetles, including more than 62,000 species [1] comprising 11 families [2,3]. They have a complex morphological structure [2–7], ecological confinement, and diverse trophic links [1], which makes them a convenient group for characterizing modern and fossil biocenoses.
    [Show full text]
  • Rvk-Diss Digi
    University of Groningen Of dwarves and giants van Klink, Roel IMPORTANT NOTE: You are advised to consult the publisher's version (publisher's PDF) if you wish to cite from it. Please check the document version below. Document Version Publisher's PDF, also known as Version of record Publication date: 2014 Link to publication in University of Groningen/UMCG research database Citation for published version (APA): van Klink, R. (2014). Of dwarves and giants: How large herbivores shape arthropod communities on salt marshes. s.n. Copyright Other than for strictly personal use, it is not permitted to download or to forward/distribute the text or part of it without the consent of the author(s) and/or copyright holder(s), unless the work is under an open content license (like Creative Commons). The publication may also be distributed here under the terms of Article 25fa of the Dutch Copyright Act, indicated by the “Taverne” license. More information can be found on the University of Groningen website: https://www.rug.nl/library/open-access/self-archiving-pure/taverne- amendment. Take-down policy If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. Downloaded from the University of Groningen/UMCG research database (Pure): http://www.rug.nl/research/portal. For technical reasons the number of authors shown on this cover page is limited to 10 maximum. Download date: 01-10-2021 Of Dwarves and Giants How large herbivores shape arthropod communities on salt marshes Roel van Klink This PhD-project was carried out at the Community and Conservation Ecology group, which is part of the Centre for Ecological and Environmental Studies of the University of Groningen, The Netherlands.
    [Show full text]
  • Vol 2 Issue 4, 2009 Alcidodes Ludificator Faust. : a Serious Insect
    ISSN 0973 -4031 Vol 2 Issue 4, 2009 Alcidodes ludificator Faust. : a serious insect pest of nursery and young plantations of Gmelina arborea (Roxb.) in northeastern India N. Senthilkumar and Nizara D. Barthakur* Rain Forest Research Institute, Jorhat – 785 001, Assam, India *E-mail : [email protected] Gmelina arborea (Roxb.) an important member of the family Verbenaceae, is a commercially important fast growing deciduous tree species. The wood of this species is an excellent source for pulp and paper industries and suitable for manufacture of matchboxes splints. In India and particularly in northeast, it is grown extensively, and has substantially been contributing in timber, fodder and industrial wood. However, low productivity, poor bole form and susceptibility to various insect-pests and diseases are some of the reasons for its non-deployment at commercial scale. Although G. arborea suffers multifarious insect injuries by a complex of insect pests including 21 defoliators and 13 shoot borers, Gamari Weevil, Alcidodes ludificator Faust. (Coleoptera: Curculionidae) is one of the serious pests of nursery and young plantations of G. arborea . A. ludificator is a small weevil 5-8 mm long, dark brown in colour and with a few light coloured bands on its elytra and a very diagnostic character- head with a long snout. The insect is found clasping the growing points of main or side branches or petioles of usually younger leaves. The weevil perceives any disturbance in the surrounding it hides quickly behind the thickness of stem or branch on which it is resting. This weevil has a habit of falling down to the ground and feigning dead at the slightest jerk to their roosting site.
    [Show full text]
  • Temporal Lags and Overlap in the Diversification of Weevils and Flowering Plants
    Temporal lags and overlap in the diversification of weevils and flowering plants Duane D. McKennaa,1, Andrea S. Sequeirab, Adriana E. Marvaldic, and Brian D. Farrella aDepartment of Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138; bDepartment of Biological Sciences, Wellesley College, Wellesley, MA 02481; and cInstituto Argentino de Investigaciones de Zonas Aridas, Consejo Nacional de Investigaciones Científicas y Te´cnicas, C.C. 507, 5500 Mendoza, Argentina Edited by May R. Berenbaum, University of Illinois at Urbana-Champaign, Urbana, IL, and approved March 3, 2009 (received for review October 22, 2008) The extraordinary diversity of herbivorous beetles is usually at- tributed to coevolution with angiosperms. However, the degree and nature of contemporaneity in beetle and angiosperm diversi- fication remain unclear. Here we present a large-scale molecular phylogeny for weevils (herbivorous beetles in the superfamily Curculionoidea), one of the most diverse lineages of insects, based on Ϸ8 kilobases of DNA sequence data from a worldwide sample including all families and subfamilies. Estimated divergence times derived from the combined molecular and fossil data indicate diversification into most families occurred on gymnosperms in the Jurassic, beginning Ϸ166 Ma. Subsequent colonization of early crown-group angiosperms occurred during the Early Cretaceous, but this alone evidently did not lead to an immediate and ma- jor diversification event in weevils. Comparative trends in weevil diversification and angiosperm dominance reveal that massive EVOLUTION diversification began in the mid-Cretaceous (ca. 112.0 to 93.5 Ma), when angiosperms first rose to widespread floristic dominance. These and other evidence suggest a deep and complex history of coevolution between weevils and angiosperms, including codiver- sification, resource tracking, and sequential evolution.
    [Show full text]
  • 3.7.10 Curculioninae Latreille, 1802 Jetzt Beschriebenen Palaearctischen Ceuthor- Rhynchinen
    Curculioninae Latreille, 1802 305 Schultze, A. (1902): Kritisches Verzeichniss der bis 3.7.10 Curculioninae Latreille, 1802 jetzt beschriebenen palaearctischen Ceuthor- rhynchinen. – Deutsche Entomologische Zeitschrift Roberto Caldara , Nico M. Franz, and Rolf 1902: 193 – 226. G. Oberprieler Schwarz, E. A. (1894): A “ parasitic ” scolytid. – Pro- ceedings of the Entomological Society of Washington 3: Distribution. The subfamily as here composed (see 15 – 17. Phylogeny and Taxonomy below) includes approx- Scudder, S. H. (1893): Tertiary Rhynchophorous Coleo- ptera of the United States. xii + 206 pp. US Geological imately 350 genera and 4500 species (O ’ Brien & Survey, Washington, DC. Wibmer 1978; Thompson 1992; Alonso-Zarazaga Stierlin, G. (1886): Fauna insectorum Helvetiae. Coleo- & Lyal 1999; Oberprieler et al. 2007), provisionally ptera helvetiae , Volume 2. 662 pp. Rothermel & Cie., divided into 34 tribes. These are geographically Schaffhausen. generally restricted to a lesser or larger degree, only Thompson, R. T. (1973): Preliminary studies on the two – Curculionini and Rhamphini – being virtually taxonomy and distribution of the melon weevil, cosmopolitan in distribution and Anthonomini , Acythopeus curvirostris (Boheman) (including Baris and Tychiini only absent from the Australo-Pacifi c granulipennis (Tournier)) (Coleoptera, Curculion- region. Acalyptini , Cionini , Ellescini , Mecinini , idae). – Bulletin of Entomological Research 63: 31 – 48. and Smicronychini occur mainly in the Old World, – (1992): Observations on the morphology and clas- from Africa to the Palaearctic and Oriental regions, sifi cation of weevils (Coleoptera, Curculionidae) with Ellescini, Acalyptini, and Smicronychini also with a key to major groups. – Journal of Natural His- extending into the Nearctic region and at least tory 26: 835 – 891. the latter two also into the Australian one.
    [Show full text]
  • Amphiesmeno- Ptera: the Caddisflies and Lepidoptera
    CY501-C13[548-606].qxd 2/16/05 12:17 AM Page 548 quark11 27B:CY501:Chapters:Chapter-13: 13Amphiesmeno-Amphiesmenoptera: The ptera:Caddisflies The and Lepidoptera With very few exceptions the life histories of the orders Tri- from Old English traveling cadice men, who pinned bits of choptera (caddisflies)Caddisflies and Lepidoptera (moths and butter- cloth to their and coats to advertise their fabrics. A few species flies) are extremely different; the former have aquatic larvae, actually have terrestrial larvae, but even these are relegated to and the latter nearly always have terrestrial, plant-feeding wet leaf litter, so many defining features of the order concern caterpillars. Nonetheless, the close relationship of these two larval adaptations for an almost wholly aquatic lifestyle (Wig- orders hasLepidoptera essentially never been disputed and is supported gins, 1977, 1996). For example, larvae are apneustic (without by strong morphological (Kristensen, 1975, 1991), molecular spiracles) and respire through a thin, permeable cuticle, (Wheeler et al., 2001; Whiting, 2002), and paleontological evi- some of which have filamentous abdominal gills that are sim- dence. Synapomorphies linking these two orders include het- ple or intricately branched (Figure 13.3). Antennae and the erogametic females; a pair of glands on sternite V (found in tentorium of larvae are reduced, though functional signifi- Trichoptera and in basal moths); dense, long setae on the cance of these features is unknown. Larvae do not have pro- wing membrane (which are modified into scales in Lepi- legs on most abdominal segments, save for a pair of anal pro- doptera); forewing with the anal veins looping up to form a legs that have sclerotized hooks for anchoring the larva in its double “Y” configuration; larva with a fused hypopharynx case.
    [Show full text]
  • Beetles in a Suburban Environment: a New Zealand Case Study. The
    tl n brbn nvrnnt: lnd td tl n brbn nvrnnt: lnd td h Idntt nd tt f Clptr n th ntrl nd dfd hbtt f nfld Alnd (4-8 GKhl . : rh At SI lnt rttn Mnt Albrt rh Cntr rvt Alnd lnd • SI lnt rttn prt • EW EAA EAME O SCIEIIC A IUSIA ESEAC 199 O Ο Ν Ε W Ε Ν ttr Grnt rd Τ Ε Ρ Ο Ι Ο Τ ie wi e suo o a oey Sciece eseac Ga om e ew eaa oey Gas oa is suo is gaeuy ackowege Ρ EW EAA SI ' EAME O lnt SCIEIIC A rttn IUSIA Wāhn ESEAC Mn p Makig Sciece Wok o ew eaa KUSCE G eees i a suua eiome a ew eaa case suy e ieiy a saus o Coeoea i e aua a moiie aias o yie Aucka (197-199 / G Kusce — Aucka SI 199 (SI a oecio eo ISS 11-1 ; o3 IS -77-59- I ie II Seies UC 5957(93111 © Cow Coyig uise y SI a oecio M Ae eseac Cee iae ag Aucka ew eaa eceme 199 ie y Geea iig Seices eso ew eaa Etiam pristina in aua Asο i a aua seig summa securitas et futura sweet tranquility and nature ., OISIECE e oe-eeig emoyci eee ioycus uuus (ou o is aie ooca os kaikaea (acycaus acyioies om e yie eee suey aea Aucka ew eaa e wie gaues o e eee ae oe cuses a ass ees is eee as a eic saus o uike a o e uaaa (Seoo as ossi eiece sows a e weei gou was iig i uassic imes way ack i e ea o e iosaus a gymosems moe a 1 miio yeas ago OEWO As a small boy in the 1930s I used to collect butterflies on the South Downs in southern England.
    [Show full text]
  • Papilionidae)
    180 JOURNAL OF THE LEPIDOPTERISTS' SOCIETY NOTES ON THE BIOLOGIES OF PAPILlO LAGLAIZEI AND P. TOBOROI (PAPILIONIDAE) R. STRAATMAN Sogeri, Papua, New Guinea Papilio laglaizei Depuiset and P. toboroi Ribbe are included in a small and closely related species group that is morphologically distinctive from other species in the genus (Munroe, 1958). P. laglaizei is found on mainland New Guinea, and P. tohoroi occurs on Bougainville, Santa Ysabel and Malaita Island. A third species, P. moerneri Aurivillius, is known from New Ireland. What some recognise as P. mayrhoferi Bang-Haas from New Britain probably is only a geographical race of P. moerneri as was originally described by Bang-Haas (1939). In addition to the two specimens of typical P. moerneri mentioned by D'Abrera (1971), there is one in the Australian National Insect Collec­ tion, Canberra, and the author has also seen a few specimens taken on New Ireland in 1968. In view of the foregoing, and the fact that at least some known localities of the species on New Ireland have hardly been disturbed during this century, D'Abrera's (op. cit.) suggestion that the species is "probably extinct" is considered unlikely to be correct. The adult of P. laglaizei shows a remarkable similarity to the common and presumably distasteful diurnal moth Alcides agathyrsus Kirsch (Uraniidae). The two species also share some of the same habitats. These factors suggest a possible mimicry situation. Papilio tohoroi and P. moerneri, although co-existing in the same habitats with other diurnal Alcides species, do not particularly resemble them. The biology of this Papilio species group is remarkable in other aspects, e.g., the laying of eggs in large masses and the highly gregarious behaviour of the larvae (D'Abrera, 1971).
    [Show full text]