A Tribute to Guillermo (Willy) Kuschel (1918–2017)
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Classical Biological Control of Arthropods in Australia
Classical Biological Contents Control of Arthropods Arthropod index in Australia General index List of targets D.F. Waterhouse D.P.A. Sands CSIRo Entomology Australian Centre for International Agricultural Research Canberra 2001 Back Forward Contents Arthropod index General index List of targets The Australian Centre for International Agricultural Research (ACIAR) was established in June 1982 by an Act of the Australian Parliament. Its primary mandate is to help identify agricultural problems in developing countries and to commission collaborative research between Australian and developing country researchers in fields where Australia has special competence. Where trade names are used this constitutes neither endorsement of nor discrimination against any product by the Centre. ACIAR MONOGRAPH SERIES This peer-reviewed series contains the results of original research supported by ACIAR, or material deemed relevant to ACIAR’s research objectives. The series is distributed internationally, with an emphasis on the Third World. © Australian Centre for International Agricultural Research, GPO Box 1571, Canberra ACT 2601, Australia Waterhouse, D.F. and Sands, D.P.A. 2001. Classical biological control of arthropods in Australia. ACIAR Monograph No. 77, 560 pages. ISBN 0 642 45709 3 (print) ISBN 0 642 45710 7 (electronic) Published in association with CSIRO Entomology (Canberra) and CSIRO Publishing (Melbourne) Scientific editing by Dr Mary Webb, Arawang Editorial, Canberra Design and typesetting by ClarusDesign, Canberra Printed by Brown Prior Anderson, Melbourne Cover: An ichneumonid parasitoid Megarhyssa nortoni ovipositing on a larva of sirex wood wasp, Sirex noctilio. Back Forward Contents Arthropod index General index Foreword List of targets WHEN THE CSIR Division of Economic Entomology, now Commonwealth Scientific and Industrial Research Organisation (CSIRO) Entomology, was established in 1928, classical biological control was given as one of its core activities. -
Coleoptera: Staphylinidae: Scydmaeninae) on Oribatid Mites: Prey Preferences and Hunting Behaviour
Eur. J. Entomol. 110(2): 339–353, 2013 http://www.eje.cz/pdfs/110/2/339 ISSN 1210-5759 (print), 1802-8829 (online) Specialized feeding of Euconnus pubicollis (Coleoptera: Staphylinidae: Scydmaeninae) on oribatid mites: Prey preferences and hunting behaviour 1 2 PAWEŁ JAŁOSZYŃSKI and ZIEMOWIT OLSZANOWSKI 1 Museum of Natural History, Wrocław University, Sienkiewicza 21, 50-335 Wrocław, Poland; e-mail: [email protected] 2 Department of Animal Taxonomy and Ecology, A. Mickiewicz University, Umultowska 89, 61-614 Poznań, Poland; e-mail: [email protected] Key words. Coleoptera, Staphylinidae, Scydmaeninae, Cyrtoscydmini, Euconnus, Palaearctic, prey preferences, feeding behaviour, Acari, Oribatida Abstract. Prey preferences and feeding-related behaviour of a Central European species of Scydmaeninae, Euconnus pubicollis, were studied under laboratory conditions. Results of prey choice experiments involving 50 species of mites belonging to 24 families of Oribatida and one family of Uropodina demonstrated that beetles feed mostly on ptyctimous Phthiracaridae (over 90% of prey) and only occasionally on Achipteriidae, Chamobatidae, Steganacaridae, Oribatellidae, Ceratozetidae, Euphthiracaridae and Galumni- dae. The average number of mites consumed per beetle per day was 0.27 ± 0.07, and the entire feeding process took 2.15–33.7 h and showed a clear linear relationship with prey body length. Observations revealed a previously unknown mechanism for capturing prey in Scydmaeninae in which a droplet of liquid that exudes from the mouth onto the dorsal surface of the predator’s mouthparts adheres to the mite’s cuticle. Morphological adaptations associated with this strategy include the flattened distal parts of the maxillae, whereas the mandibles play a minor role in capturing prey. -
Zootaxa, Coleoptera, Attelabidae, Apoderinae, Hoplapoderini
Zootaxa 1089: 37–47 (2005) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA 1089 Copyright © 2005 Magnolia Press ISSN 1175-5334 (online edition) A new genus and species of Hoplapoderini from Madagascar (Coleoptera: Attelabidae: Apoderinae) SILVANO BIONDI Via E. di Velo 137, I-36100 Vicenza - Italy. email: [email protected] Abstract Madapoderus pacificus, a new genus and species of hoplapoderine attelabid beetles, is described from Madagascar. A key to the genera of Hoplapoderini and field observations on the host plant and reproductive behaviour of the new species are provided. Key words: Attelabidae, Apoderinae, Hoplapoderini, Madagascar, new genus, new species, Grewia Introduction In May 2002, among specimens of Attelabidae collected in Madagascar by David Hauck some months earlier, I received two males belonging to the apoderine tribe Hoplapoderini that could not be assigned to any known genus. A study of the rich collection of Madagascan attelabids at the Muséum National d’Histoire Naturelle, Paris, a few months later confirmed this diagnosis. During a month-long collecting expedition in Madagascar in December 2003 and January 2004, I collected the new taxon again, at a different locality, and could carry out some observations on its behaviour. Systematics Tribe Hoplapoderini Voss, 1926 Voss (1926) defined his tribe Hoplapoderini largely on the basis of features of the head and elytra. The new Madagascan genus fits into this tribe due to its tapered head, with maximum width near the basis, and its tuberculate elytra. Voss also provided a key to the Accepted by Q. Wang: 7 Oct. 2005; published: 2 Dec. 2005 37 ZOOTAXA genera of the tribe, but this is largely inadequate because of its heavy reliance on the 1089 presence and shape of what he called “abdominal lobes” (“Abdominallappen”). -
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 -
Fossil History of Curculionoidea (Coleoptera) from the Paleogene
geosciences Review Fossil History of Curculionoidea (Coleoptera) from the Paleogene Andrei A. Legalov 1,2 1 Institute of Systematics and Ecology of Animals, Siberian Branch, Russian Academy of Sciences, Ulitsa Frunze, 11, 630091 Novosibirsk, Novosibirsk Oblast, Russia; [email protected]; Tel.: +7-9139471413 2 Biological Institute, Tomsk State University, Lenin Ave, 36, 634050 Tomsk, Tomsk Oblast, Russia Received: 23 June 2020; Accepted: 4 September 2020; Published: 6 September 2020 Abstract: Currently, some 564 species of Curculionoidea from nine families (Nemonychidae—4, Anthribidae—33, Ithyceridae—3, Belidae—9, Rhynchitidae—41, Attelabidae—3, Brentidae—47, Curculionidae—384, Platypodidae—2, Scolytidae—37) are known from the Paleogene. Twenty-seven species are found in the Paleocene, 442 in the Eocene and 94 in the Oligocene. The greatest diversity of Curculionoidea is described from the Eocene of Europe and North America. The richest faunas are known from Eocene localities, Florissant (177 species), Baltic amber (124 species) and Green River formation (75 species). The family Curculionidae dominates in all Paleogene localities. Weevil species associated with herbaceous vegetation are present in most localities since the middle Paleocene. A list of Curculionoidea species and their distribution by location is presented. Keywords: Coleoptera; Curculionoidea; fossil weevil; faunal structure; Paleocene; Eocene; Oligocene 1. Introduction Research into the biodiversity of the past is very important for understanding the development of life on our planet. Insects are one of the Main components of both extinct and recent ecosystems. Coleoptera occupied a special place in the terrestrial animal biotas of the Mesozoic and Cenozoics, as they are characterized by not only great diversity but also by their ecological specialization. -
The Evolution and Genomic Basis of Beetle Diversity
The evolution and genomic basis of beetle diversity Duane D. McKennaa,b,1,2, Seunggwan Shina,b,2, Dirk Ahrensc, Michael Balked, Cristian Beza-Bezaa,b, Dave J. Clarkea,b, Alexander Donathe, Hermes E. Escalonae,f,g, Frank Friedrichh, Harald Letschi, Shanlin Liuj, David Maddisonk, Christoph Mayere, Bernhard Misofe, Peyton J. Murina, Oliver Niehuisg, Ralph S. Petersc, Lars Podsiadlowskie, l m l,n o f l Hans Pohl , Erin D. Scully , Evgeny V. Yan , Xin Zhou , Adam Slipinski , and Rolf G. Beutel aDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; bCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; cCenter for Taxonomy and Evolutionary Research, Arthropoda Department, Zoologisches Forschungsmuseum Alexander Koenig, 53113 Bonn, Germany; dBavarian State Collection of Zoology, Bavarian Natural History Collections, 81247 Munich, Germany; eCenter for Molecular Biodiversity Research, Zoological Research Museum Alexander Koenig, 53113 Bonn, Germany; fAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; gDepartment of Evolutionary Biology and Ecology, Institute for Biology I (Zoology), University of Freiburg, 79104 Freiburg, Germany; hInstitute of Zoology, University of Hamburg, D-20146 Hamburg, Germany; iDepartment of Botany and Biodiversity Research, University of Wien, Wien 1030, Austria; jChina National GeneBank, BGI-Shenzhen, 518083 Guangdong, People’s Republic of China; kDepartment of Integrative Biology, Oregon State -
Arthropods of Elm Fork Preserve
Arthropods of Elm Fork Preserve Arthropods are characterized by having jointed limbs and exoskeletons. They include a diverse assortment of creatures: Insects, spiders, crustaceans (crayfish, crabs, pill bugs), centipedes and millipedes among others. Column Headings Scientific Name: The phenomenal diversity of arthropods, creates numerous difficulties in the determination of species. Positive identification is often achieved only by specialists using obscure monographs to ‘key out’ a species by examining microscopic differences in anatomy. For our purposes in this survey of the fauna, classification at a lower level of resolution still yields valuable information. For instance, knowing that ant lions belong to the Family, Myrmeleontidae, allows us to quickly look them up on the Internet and be confident we are not being fooled by a common name that may also apply to some other, unrelated something. With the Family name firmly in hand, we may explore the natural history of ant lions without needing to know exactly which species we are viewing. In some instances identification is only readily available at an even higher ranking such as Class. Millipedes are in the Class Diplopoda. There are many Orders (O) of millipedes and they are not easily differentiated so this entry is best left at the rank of Class. A great deal of taxonomic reorganization has been occurring lately with advances in DNA analysis pointing out underlying connections and differences that were previously unrealized. For this reason, all other rankings aside from Family, Genus and Species have been omitted from the interior of the tables since many of these ranks are in a state of flux. -
A Systematic Study of the Family Rhynchitidae of Japan(Coleoptera
Humans and Nature. No. 2, 1 ―93, March 1993 A Systematic Study of the Family Rhynchitidae of Japan (Coleoptera, Curculionoidea) * Yoshihisa Sawada Division of Phylogenetics, Museum of Nature and Human Activities, Hyogo, Yayoi~ga~oka 6, Sanda, 669~ 13 fapan Abstract Japanese RHYNCHITIDAE are systematically reviewed and revised. Four tribes, 17 genera and 62 species are recognized. Original and additional descriptions are given, with illustrations of and keys to their taxa. The generic and subgeneric names of Voss' system are reviewed from the viewpoint of nomenclature. At the species level, 12 new species Auletobius planifrons, Notocyrtus caeligenus, Involvulus flavus, I. subtilis, I. comix, I. aes, I. lupulus, Deporaus tigris, D. insularis, D. eumegacephalus, D. septemtrionalis and D. rhynchitoides are described and 1 species Engnamptus sauteri are newly recorded from Japan. Six species and subspecies names Auletes carvus, A. testaceus and A. irkutensis japonicus, Auletobius okinatuaensis, Aderorhinus pedicellaris nigricollis and Rhynchites cupreus purpuleoviolaceus are synonymized under Auletobius puberulus, A. jumigatus, A. uniformis, Ad. crioceroides and I. cylindricollis, respectively. One new name Deporaus vossi is given as the replacement name of the primally junior homonym D. pallidiventris Voss, 1957 (nec Voss, 1924). Generic and subgeneric classification is revised in the following points. The genus Notocyrtus is revived as an independent genus including subgenera Notocyrtus s. str., Exochorrhynchites and Heterorhynchites. Clinorhynckites and Habrorhynchites are newly treated as each independent genera. Caenorhinus is newly treated as a valid subgenus of the genus Deporaus. The genera Neocoenorrhinus and Piazorhynckites are newly synonymized under Notocyrtus and Agilaus, respectively, in generic and subgeneric rank. A subgeneric name, Aphlorhynehites subgen. -
Revista Chilena De Entomología, Now in (Nemestrinids) and Ureta (Lepidoptera)
Rev. Chilena Ent, 1974, 8: 6-10 INSECTS — MEN AND ENVIRONMENT IN CHILE Dr. LUCIANO E. CAMPOS (*) We Chileans have boasted for much too huge pioneer enterprise that from 1844 long that our country, in the Southern up to 1871, two years before his death in tip and Western slopes of South Ame- France, he released under his authorship,^ rica, is a biological and ecológica! island, printed in Paris and in Spanish, his isolated to the North by a dry desert monumental "Historia Física y Política 800 miles long; by the tallest range of de Chile", in 28 volumes and two large mountains, the Andes, to the East ; by the Atlases, covering some 15.000 printed largest Ocean to the West; and by the pages, and the description of about 2.500 wind swept freezing encounter of two plants, animáis and Insects from the vast seas in the Strait of Magellan and country he strenuously surveyed for years, the Beagle Channel to the South. preferably on the back of a horse! i This notion of geographical isolation of We will have to mention again this Chile was first noted by a distinguished outstanding "Chilean citizen", as he French naturalist during the ten years proudly referred to himself, who found in he lived in the countiy, and published in Chile, a just born-to-freedom disorganized 1845 (**). nation, an unexpected thorough meaning This man was Claudio Gay, who carne and a full sense of purpose for the 43 to Chile in 1829 and was commissioned in remaining years of his long life. -
Lepidoptera Fauna of Namibia. I. Seasonal Distribution of Moths of the Koakoland (Mopane) Savanna in Ogongo, Northern Namibia
FRAGMENTA FAUNISTICA 57 (2): 117–129, 2014 PL ISSN 0015-9301 © MUSEUM AND INSTITUTE OF ZOOLOGY PAS DOI 10.3161/00159301FF2014.57.2.117 Lepidoptera fauna of Namibia. I. Seasonal distribution of moths of the Koakoland (Mopane) Savanna in Ogongo, northern Namibia Grzegorz KOPIJ Department of Wildlife Management, University of Namibia, Katima Mulilio Campus, Private Bag 1096, Katima Mulilo, Namibia; e-mail: [email protected] Abstract: During the years 2011–2013, moths were collected in Koakoland (Mopane) Savanna in the Cuvelai Drainage System, Ovamboland, northern Namibia. In total, 77 species from 13 families have been identified. Their seasonal occurrence in this habitat was also investigated, with most species recorded in wet season between September and April, but with clear peak in February and March. The family Noctuidae was by far the most speciose (38 recorded species), followed by Crambidae (8 spp.), Sphingidae (6 spp.) and Arctiidae (4 spp.). All other families were represented by 1–3 species. For each species listed date of collection is given, and data on its global distribution. Key words: Lepidoptera, check-list, biodiversity, distribution, moths, Ovamboland INTRODUCTION According to recent quite precise estimate, there are 15 5181 species, 16 650 genera and 121 families of Lepidoptera worldwide (Pouge 2009). Lepidoptera fauna of Namibia has recently attracted attention of European entomologists. However, thorough surveys were conducted hitherto in a few areas only, such as Brandberg and Hobatere. The northern regions of the country were especially badly neglected. In southern Africa (south of Zambezi and Kunene Rivers) – 8 511 species, 2 368 genera and 89 families were recently catalogued (Vári et al. -
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. -
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.