Beetles of Conservation Interest from the Three Kings Islands
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Wildlife Act 1953
Reprint as at 7 August 2020 Wildlife Act 1953 Public Act 1953 No 31 Date of assent 31 October 1953 Commencement see section 1(2) Contents Page Title 7 1 Short Title and commencement 7 2 Interpretation 7 2A Meaning of possession 14 2B Application of certain provisions restricted 15 Part 1 Protection of wildlife 3 Wildlife to be protected 15 4 Certain wildlife declared to be game 16 5 Certain wildlife partially protected 16 6 Certain wildlife may be hunted subject to conditions imposed by 16 the Minister 7 Certain wildlife not protected 17 7A Wild animals 17 7B Terrestrial and freshwater invertebrates 18 7BA Marine species 18 7C Farming certain unprotected animals 18 8 Alteration of schedules 19 Note Changes authorised by subpart 2 of Part 2 of the Legislation Act 2012 have been made in this official reprint. Note 4 at the end of this reprint provides a list of the amendments incorporated. This Act is administered by the Department of Conservation. 1 Reprinted as at Wildlife Act 1953 7 August 2020 Wildlife sanctuaries 9 Wildlife sanctuaries 19 10 All wildlife in sanctuaries absolutely protected 23 11 Destruction or seizure of certain animals found in sanctuaries 24 12 Mining privileges, coal mining rights, and public works 24 [Repealed] 13 Seizure of wildlife, etc, illegally taken 24 Wildlife refuges 14 Wildlife refuges 25 Wildlife management reserves 14A Wildlife management reserves 28 14AA Granting of concessions in wildlife sanctuaries, wildlife refuges, 30 and wildlife management reserves Management planning 14B Wildlife areas to be -
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 -
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 -
(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. -
New Locality Records for Two Species of Protected Weevils, Anagotus Fairburni
Tuhinga 29: 20–34 Copyright © Museum of New Zealand Te Papa Tongarewa (2018) New locality records for two species of protected weevils, Anagotus fairburni (Brookes, 1932) and Hadramphus stilbocarpae Kuschel, 1971 (Coleoptera: Curculionidae), from southern Fiordland, New Zealand Colin M. Miskelly,* Alan J.D. Tennyson** and Colin R. Bishop*** * Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington 6140, New Zealand ([email protected]) ** Museum of New Zealand Te Papa Tongarewa, PO Box 467, Wellington 6140, New Zealand *** Department of Conservation, PO Box 29, Te Anau 9600, New Zealand ABSTRACT: The flax weevil Anagotus fairburni (Brookes, 1932) and knobbled weevil Hadramphus stilbocarpae Kuschel, 1971 were among the first New Zealand insects to be granted legal protection. Both are large flightless species with narrow host–plant requirements. Their disjunct distributions are probably the result of predation by introduced rodents, with populations of both having apparently been extirpated by ship rats (Rattus rattus) at one documented site (Taukihepa/Big South Cape Island). Within Fiordland, flax weevils were previously known from a single small island in Breaksea Sound, and knobbled weevils had been reported from five outer islands, from Secretary Island south to Resolution Island. We report the presence of both species in Dusky Sound, and flax weevils in Chalky and Preservation Inlets, based on surveys of 134 islands in 2016 and 2017. Signs of flax weevil feeding were recorded on 56 widely scattered islands, with live or dead animals found on seven of these during the limited search time available. A single knobbled weevil was found at night on a small island in the Seal Islands, southwest of Anchor Island. -
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. -
Micro-CT to Document the Coffee Bean Weevil, Araecerus Fasciculatus (Coleoptera: Anthribidae), Inside Field-Collected Coffee Berries (Coffea Canephora)
insects Communication Micro-CT to Document the Coffee Bean Weevil, Araecerus fasciculatus (Coleoptera: Anthribidae), Inside Field-Collected Coffee Berries (Coffea canephora) Ignacio Alba-Alejandre 1 ID , Javier Alba-Tercedor 1 ID and Fernando E. Vega 2,* ID 1 Department of Zoology, Faculty of Sciences, University of Granada, Campus de Fuentenueva, 18071 Granada, Spain; [email protected] (I.A.-A.); [email protected] (J.A.-T.) 2 Sustainable Perennial Crops Laboratory, United States Department of Agriculture, Agricultural Research Service, Beltsville, MD 20705, USA * Correspondence: [email protected]; Tel.: +1-301-504-5101 Received: 22 June 2018; Accepted: 10 August 2018; Published: 14 August 2018 Abstract: The coffee bean weevil, Araecerus fasciculatus (De Geer) (Coleoptera: Anthribidae), is a cosmopolitan insect with >100 hosts, and has been reported as a pest of stored coffee. During a study involving the coffee berry borer, we observed coffee bean weevils emerging from field-collected coffee berries and used micro-computerized tomography (micro-CT) scans to observe the insect inside the berry. Two eggs had eclosed inside the berry, resulting in observations of a newly eclosed adult beetle and a 5th instar larva, each feeding on one of the two seeds. This is the first time since 1775, when the insect was first described, that the insect has been observed inside a coffee berry. Keywords: coffee quality; insect biology; losses; stored coffee; stored product pest 1. Introduction The genus Araecerus Schönherr comprises ca. 75 species [1], with the coffee bean weevil, Araecerus fasciculatus (De Geer) (Coleoptera: Anthribidae), being the most economically important. Chittenden [2,3] coined the name coffee bean weevil and Valentine [1] has published a succinct account on the controversy involving the many different scientific names used for the insect. -
ANTHRIBIDAE (Fungus Weevils)
FAMILY ANTHRIBIDAE (Fungus weevils) J. McNamara This family includes 18 species in Canada and Alaska. One of these, the Coffee Bean Weevil, is introduced and may be established in warehouses; this species damages many stored plant materials including seeds. Adults of anthribids are often collected by beating dead or diseased vegetation or by sweeping in weedy areas. The larvae are usually found in similar habitats. Adults feed on fungi, pollen or even bark; larvae feed in plant stems, fungi or woods. The North American genera of Anthribidae have been revised by Valentine (1960); the Canadian species are being revised by Bright and his work is expected to be published soon in the Handbook series "The Insects and Arachnids of Canada". AK (2); YK (2); NT (2); BC (4); AB (8); SK (6); MB (7); ON (12); PQ (11); NB (1); NS (1); NF (1); H (1); I (1) Subfamily CHORAGINAE Tribe Araecerini Genus ARAECERUS Schonherr A. fasciculatus (DeGeer)+ - - - BC - - - ON - - - - - - Tribe Choragini Genus EUXENUS LeConte E. punctatus LeConte - - - - - - - - PQ - - - - - Subfamily ANTHRIBINAE Tribe Eupariini Genus EUPARIUS Schonherr Key to North American species: Valentine (1960) E. marmoreus (Olivier) - - - - - - MB ON PQ NB - - - - albifrons (Boheman) lunatus (Fabricius) Tribe Anthribini Genus TRIGONORHINUS Wollaston Anthribulus LeConte Brachytarsoides Pierce Key to Western North American species: Valentine (1971) T. alternatus (Say) - - - - AB - MB ON - - - - - - T. annulatus (Carr) - - - BC AB - - - - - - - - - T. griseus (LeConte) - - - - AB SK - - - - - - - - T. limbatus (Say) - - - - AB SK MB ON PQ - - - - - T. sticticus (Boheman) - - NT BC AB SK MB ON PQ - - - - - obsoletus (Fahreus) variegatus (Say) T. tomentosus tomentosus (Say) - - - - - - - ON - - - - - - brevis (Fahreus) paululus (Casey) Tribe Ormiscini Genus ORMISCUS Waterhouse Eusphyrus LeConte Gonops LeConte Toxotropis LeConte O. -
Weevils) of the George Washington Memorial Parkway, Virginia
September 2020 The Maryland Entomologist Volume 7, Number 4 The Maryland Entomologist 7(4):43–62 The Curculionoidea (Weevils) of the George Washington Memorial Parkway, Virginia Brent W. Steury1*, Robert S. Anderson2, and Arthur V. Evans3 1U.S. National Park Service, 700 George Washington Memorial Parkway, Turkey Run Park Headquarters, McLean, Virginia 22101; [email protected] *Corresponding author 2The Beaty Centre for Species Discovery, Research and Collection Division, Canadian Museum of Nature, PO Box 3443, Station D, Ottawa, ON. K1P 6P4, CANADA;[email protected] 3Department of Recent Invertebrates, Virginia Museum of Natural History, 21 Starling Avenue, Martinsville, Virginia 24112; [email protected] ABSTRACT: One-hundred thirty-five taxa (130 identified to species), in at least 97 genera, of weevils (superfamily Curculionoidea) were documented during a 21-year field survey (1998–2018) of the George Washington Memorial Parkway national park site that spans parts of Fairfax and Arlington Counties in Virginia. Twenty-three species documented from the parkway are first records for the state. Of the nine capture methods used during the survey, Malaise traps were the most successful. Periods of adult activity, based on dates of capture, are given for each species. Relative abundance is noted for each species based on the number of captures. Sixteen species adventive to North America are documented from the parkway, including three species documented for the first time in the state. Range extensions are documented for two species. Images of five species new to Virginia are provided. Keywords: beetles, biodiversity, Malaise traps, national parks, new state records, Potomac Gorge. INTRODUCTION This study provides a preliminary list of the weevils of the superfamily Curculionoidea within the George Washington Memorial Parkway (GWMP) national park site in northern Virginia. -
The Evolutionary History of the Coleoptera
geosciences Editorial The Evolutionary History of the Coleoptera Alexander G. Kirejtshuk Zoological Institute, Russian Academy of Sciences, Universitetskaya emb. 1, St. Petersburg 199034, Russia; [email protected] or [email protected] Received: 29 January 2020; Accepted: 5 March 2020; Published: 12 March 2020 Abstract: In this Editorial, different aspects of palaeocoleopterological studies and contributions of the issue “The Evolutionary History of the Coleoptera” are discussed. Keywords: classification; problems of taxonomic interpretation of fossils; contributions for studies of palaeoenvironment and faunogenesis “Beetles, like other insects, spread quickly and practically simultaneously (in the geological sense), appearing in different parts of the Earth. The differences in dispersal result not from the difficulty to reach a particular location of the Earth, but because of the difficulty to enter an ecosystem already formed. Thus, the evolutionary potential of beetles is quite high, and the study of their ancient representatives is interesting from many points of view; however, it requires much effort and expertise. Unfortunately, a study of the palaeontology of beetles is a much more complicated task than that of Hymenoptera or Diptera. By the structure of the wing of the latter it is nearly always possible to determine to what large taxon it belongs. For the majority of discoveries of isolated elytra of beetles at the present state of knowledge it is impossible to identify the group to which the beetle with these elytra belongs. However there was a period—the Permian except its very end—when the evolution of elytra was the main evolutionary process in beetles.” Ponomarenko, A.G. Paleontological discoveries of beetles. -
Island Restoration: Seabirds, Predators, and the Importance of History
AvailableBellingham on-line et al.: at: Island http://www.newzealandecology.org/nzje/ restoration 115 special issue: Feathers to Fur The ecological transformation of Aotearoa/New Zealand New Zealand island restoration: seabirds, predators, and the importance of history Peter J. Bellingham1*, David R. Towns2, Ewen K. Cameron3, Joe J. Davis4, David A. Wardle1, 5, Janet M. Wilmshurst1 and Christa P.H. Mulder6 1Landcare Research, PO Box 40, Lincoln 7640, New Zealand 2Department of Conservation, Private Bag 68-908, Auckland, New Zealand 3Auckland Museum, Private Bag 92018, Auckland, New Zealand 4Ngāti Hei Trust, PO Box 250, Whitianga, New Zealand 5Department of Forest Vegetation Ecology, Swedish University of Agricultural Sciences, S 901 83 Umeå, Sweden 6Department of Biology and Wildlife & Institute of Arctic Biology, University of Alaska Fairbanks, AK 99775, USA *Author for correspondence (Email: [email protected]) Published online: 6 October 2009 Abstract: New Zealand’s offshore and outlying islands have long been a focus of conservation biology as sites of local endemism and as last refuges for many species. During the c. 730 years since New Zealand has been settled by people, mammalian predators have invaded many islands and caused local and global extinctions. New Zealand has led international efforts in island restoration. By the late 1980s, translocations of threatened birds to predator-free islands were well under way to safeguard against extinction. Non-native herbivores and predators, such as goats and cats, had been eradicated from some islands. A significant development in island restoration in the mid-1980s was the eradication of rats from small forested islands. This eradication technology has been refined and currently at least 65 islands, including large and remote Campbell (11 216 ha) and Raoul (2938 ha) Islands, have been successfully cleared of rats. -
Fifty Million Years of Beetle Evolution Along the Antarctic Polar Front
Fifty million years of beetle evolution along the Antarctic Polar Front Helena P. Bairda,1, Seunggwan Shinb,c,d, Rolf G. Oberprielere, Maurice Hulléf, Philippe Vernong, Katherine L. Moona, Richard H. Adamsh, Duane D. McKennab,c,2, and Steven L. Chowni,2 aSchool of Biological Sciences, Monash University, Clayton, VIC 3800, Australia; bDepartment of Biological Sciences, University of Memphis, Memphis, TN 38152; cCenter for Biodiversity Research, University of Memphis, Memphis, TN 38152; dSchool of Biological Sciences, Seoul National University, Seoul 08826, Republic of Korea; eAustralian National Insect Collection, Commonwealth Scientific and Industrial Research Organisation, Canberra, ACT 2601, Australia; fInstitut de Génétique, Environnement et Protection des Plantes, Institut national de recherche pour l’agriculture, l’alimentation et l’environnement, Université de Rennes, 35653 Le Rheu, France; gUniversité de Rennes, CNRS, UMR 6553 ECOBIO, Station Biologique, 35380 Paimpont, France; hDepartment of Computer and Electrical Engineering and Computer Science, Florida Atlantic University, Boca Raton, FL 33431; and iSecuring Antarctica’s Environmental Future, School of Biological Sciences, Monash University, Clayton, VIC 3800, Australia Edited by Nils Chr. Stenseth, University of Oslo, Oslo, Norway, and approved May 6, 2021 (received for review August 24, 2020) Global cooling and glacial–interglacial cycles since Antarctica’s iso- The hypothesis that diversification has proceeded similarly in lation have been responsible for the diversification of the region’s Antarctic marine and terrestrial groups has not been tested. While marine fauna. By contrast, these same Earth system processes are the extinction of a diverse continental Antarctic biota is well thought to have played little role terrestrially, other than driving established (13), mounting evidence of significant and biogeo- widespread extinctions.