T. Keith Philips
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Ancient Roaches Further Exemplify 'No Land Return' in Aquatic Insects
Gondwana Research 68 (2019) 22–33 Contents lists available at ScienceDirect Gondwana Research journal homepage: www.elsevier.com/locate/gr Ancient roaches further exemplify ‘no land return’ in aquatic insects Peter Vršanský a,b,c,d,1, Hemen Sendi e,⁎,1, Danil Aristov d,f,1, Günter Bechly g,PatrickMüllerh, Sieghard Ellenberger i, Dany Azar j,k, Kyoichiro Ueda l, Peter Barna c,ThierryGarciam a Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia b Slovak Academy of Sciences, Institute of Physics, Research Center for Quantum Information, Dúbravská cesta 9, Bratislava 84511, Slovakia c Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, P.O. BOX 106, 840 05 Bratislava, Slovakia d Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya 123, 117868 Moscow, Russia e Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava 84215, Slovakia f Cherepovets State University, Cherepovets 162600, Russia g Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, D-70191 Stuttgart, Germany h Friedhofstraße 9, 66894 Käshofen, Germany i Bodelschwinghstraße 13, 34119 Kassel, Germany j State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, PR China k Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, PO Box 26110217, Fanar - Matn, Lebanon l Kitakyushu Museum, Japan m River Bigal Conservation Project, Avenida Rafael Andrade y clotario Vargas, 220450 Loreto, Orellana, Ecuador article info abstract Article history: Among insects, 236 families in 18 of 44 orders independently invaded water. We report living amphibiotic cock- Received 13 July 2018 roaches from tropical streams of UNESCO BR Sumaco, Ecuador. -
Beetle Appreciation Diversity and Classification of Common Beetle Families Christopher E
Beetle Appreciation Diversity and Classification of Common Beetle Families Christopher E. Carlton Louisiana State Arthropod Museum Coleoptera Families Everyone Should Know (Checklist) Suborder Adephaga Suborder Polyphaga, cont. •Carabidae Superfamily Scarabaeoidea •Dytiscidae •Lucanidae •Gyrinidae •Passalidae Suborder Polyphaga •Scarabaeidae Superfamily Staphylinoidea Superfamily Buprestoidea •Ptiliidae •Buprestidae •Silphidae Superfamily Byrroidea •Staphylinidae •Heteroceridae Superfamily Hydrophiloidea •Dryopidae •Hydrophilidae •Elmidae •Histeridae Superfamily Elateroidea •Elateridae Coleoptera Families Everyone Should Know (Checklist, cont.) Suborder Polyphaga, cont. Suborder Polyphaga, cont. Superfamily Cantharoidea Superfamily Cucujoidea •Lycidae •Nitidulidae •Cantharidae •Silvanidae •Lampyridae •Cucujidae Superfamily Bostrichoidea •Erotylidae •Dermestidae •Coccinellidae Bostrichidae Superfamily Tenebrionoidea •Anobiidae •Tenebrionidae Superfamily Cleroidea •Mordellidae •Cleridae •Meloidae •Anthicidae Coleoptera Families Everyone Should Know (Checklist, cont.) Suborder Polyphaga, cont. Superfamily Chrysomeloidea •Chrysomelidae •Cerambycidae Superfamily Curculionoidea •Brentidae •Curculionidae Total: 35 families of 131 in the U.S. Suborder Adephaga Family Carabidae “Ground and Tiger Beetles” Terrestrial predators or herbivores (few). 2600 N. A. spp. Suborder Adephaga Family Dytiscidae “Predacious diving beetles” Adults and larvae aquatic predators. 500 N. A. spp. Suborder Adephaga Family Gyrindae “Whirligig beetles” Aquatic, on water -
Dung Beetle Richness, Abundance, and Biomass Meghan Gabrielle Radtke Louisiana State University and Agricultural and Mechanical College, [email protected]
Louisiana State University LSU Digital Commons LSU Doctoral Dissertations Graduate School 2006 Tropical Pyramids: Dung Beetle Richness, Abundance, and Biomass Meghan Gabrielle Radtke Louisiana State University and Agricultural and Mechanical College, [email protected] Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_dissertations Recommended Citation Radtke, Meghan Gabrielle, "Tropical Pyramids: Dung Beetle Richness, Abundance, and Biomass" (2006). LSU Doctoral Dissertations. 364. https://digitalcommons.lsu.edu/gradschool_dissertations/364 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Doctoral Dissertations by an authorized graduate school editor of LSU Digital Commons. For more information, please [email protected]. TROPICAL PYRAMIDS: DUNG BEETLE RICHNESS, ABUNDANCE, AND BIOMASS A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Biological Sciences by Meghan Gabrielle Radtke B.S., Arizona State University, 2001 May 2007 ACKNOWLEDGEMENTS I would like to thank my advisor, Dr. G. Bruce Williamson, and my committee members, Dr. Chris Carlton, Dr. Jay Geaghan, Dr. Kyle Harms, and Dr. Dorothy Prowell for their help and guidance in my research project. Dr. Claudio Ruy opened his laboratory to me during my stay in Brazil and collaborated with me on my project. Thanks go to my field assistants, Joshua Dyke, Christena Gazave, Jeremy Gerald, Gabriela Lopez, and Fernando Pinto, and to Alejandro Lopera for assisting me with Ecuadorian specimen identifications. I am grateful to Victoria Mosely-Bayless and the Louisiana State Arthropod Museum for allowing me work space and access to specimens. -
Insects in Cretaceous and Cenozoic Amber of Eurasia and North America
Insects in Cretaceous and Cenozoic Amber of Eurasia and North America Schmalhausen Institute of Zoology, National Academy of Sciences of Ukraine, ul. Bogdana Khmel’nitskogo 15, Kiev, 01601 Ukraine email: [email protected] Edited by E. E. Perkovsky ISSN 00310301, Paleontological Journal, 2016, Vol. 50, No. 9, p. 935. © Pleiades Publishing, Ltd., 2016. Preface DOI: 10.1134/S0031030116090100 The amber is wellknown as a source of the most Eocene ambers. However, based on paleobotanical valuable, otherwise inaccessible information on the data, confirmed by new paleoentomological data, it is biota and conditions in the past. The interest in study dated Middle Eocene. Detailed discussions of dating ing Mesozoic and Paleogene ambers has recently and relationships of Sakhalinian ants is provided in the sharply increased throughout the world. The studies first paper of the present volume, in which the earliest included in this volume concern Coleoptera, ant of the subfamily Myrmicinae is described from Hymenoptera, and Diptera from the Cretaceous, the Sakhalinian amber and assigned to an extant Eocene, and Miocene amber of the Taimyr Peninsula, genus. The earliest pedogenetic gall midge of the Sakhalin Island, Baltic Region, Ukraine, and Mexico. tribe Heteropezini from the Sakhalinian amber is Yantardakh is the most important Upper Creta also described here. ceous insect locality in northern Asia, which was dis The Late Eocene Baltic amber is investigated better covered by an expedition of the Paleontological Insti than any other; nevertheless, more than half of its tute of the Academy of Sciences of the USSR fauna remains undescribed; the contemporaneous (at present, Borissiak Paleontological Institute, Rus fauna from the Rovno amber is investigated to a con sian Academy of Sciences: PIN) in 1970 and addition siderably lesser degree. -
Stored Grain Insects and Pea Weevil (Live) Insects Large – Dead Or Alive
To whom it may concern, Proposal for GTA Standards change regarding Cereal grains for categories: Stored Grain Insects and Pea Weevil (live) Insects Large – dead or alive Currently there is a lack of reference with insects of NIL tolerance applied by DA for export and that listed within GTA standards. This has the potential to cause contract disputes especially in the grower direct to port transactions. At present if a supplier delivers grain with live insects for example Small-eyed flour beetles and Black fungus beetles, there is no reference in the standards that declare such insects as NIL tolerance. If the buyer was loading a container direct for export this would pose a problem due to the NIL tolerance being applied by DA for export phytosanitary requirements. These insects are in the same category as Psocids which are listed in GTA receival standards. I would like to see the GTA "Stored Grain Insects and Pea Weevil (live)" & "Insects Large – dead or alive" reflect the Department of Agriculture PEOM 6a: Pests, Diseases and Contaminants of Grain and Plant Products (excluding horticulture) http://www.agriculture.gov.au/SiteCollectionDocuments/aqis/exporting/plants-exports-operation-manual/vol6A.pdf I put forward the motion to have all major and minor injurious pests listed within PEOM 6a that apply to cereal grains to be of NIL tolerance within the GTA standards. 1) This would involve moving the Hairy Fungus Beetle Typhaea stercorea from “Insects Large – dead or alive” to the list of “Stored Grain Insects and Pea Weevil (live)”. Thus taking it from a tolerance level of 3 per half litre to NIL. -
Insects Commonly Mistaken for Mosquitoes
Mosquito Proboscis (Figure 1) THE MOSQUITO LIFE CYCLE ABOUT CONTRA COSTA INSECTS Mosquitoes have four distinct developmental stages: MOSQUITO & VECTOR egg, larva, pupa and adult. The average time a mosquito takes to go from egg to adult is five to CONTROL DISTRICT COMMONLY Photo by Sean McCann by Photo seven days. Mosquitoes require water to complete Protecting Public Health Since 1927 their life cycle. Prevent mosquitoes from breeding by Early in the 1900s, Northern California suffered MISTAKEN FOR eliminating or managing standing water. through epidemics of encephalitis and malaria, and severe outbreaks of saltwater mosquitoes. At times, MOSQUITOES EGG RAFT parts of Contra Costa County were considered Most mosquitoes lay egg rafts uninhabitable resulting in the closure of waterfront that float on the water. Each areas and schools during peak mosquito seasons. raft contains up to 200 eggs. Recreational areas were abandoned and Realtors had trouble selling homes. The general economy Within a few days the eggs suffered. As a result, residents established the Contra hatch into larvae. Mosquito Costa Mosquito Abatement District which began egg rafts are the size of a grain service in 1927. of rice. Today, the Contra Costa Mosquito and Vector LARVA Control District continues to protect public health The larva or ÒwigglerÓ comes with environmentally sound techniques, reliable and to the surface to breathe efficient services, as well as programs to combat Contra Costa County is home to 23 species of through a tube called a emerging diseases, all while preserving and/or mosquitoes. There are also several types of insects siphon and feeds on bacteria enhancing the environment. -
The Beetle Fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and Distribution
INSECTA MUNDI, Vol. 20, No. 3-4, September-December, 2006 165 The beetle fauna of Dominica, Lesser Antilles (Insecta: Coleoptera): Diversity and distribution Stewart B. Peck Department of Biology, Carleton University, 1125 Colonel By Drive, Ottawa, Ontario K1S 5B6, Canada stewart_peck@carleton. ca Abstract. The beetle fauna of the island of Dominica is summarized. It is presently known to contain 269 genera, and 361 species (in 42 families), of which 347 are named at a species level. Of these, 62 species are endemic to the island. The other naturally occurring species number 262, and another 23 species are of such wide distribution that they have probably been accidentally introduced and distributed, at least in part, by human activities. Undoubtedly, the actual numbers of species on Dominica are many times higher than now reported. This highlights the poor level of knowledge of the beetles of Dominica and the Lesser Antilles in general. Of the species known to occur elsewhere, the largest numbers are shared with neighboring Guadeloupe (201), and then with South America (126), Puerto Rico (113), Cuba (107), and Mexico-Central America (108). The Antillean island chain probably represents the main avenue of natural overwater dispersal via intermediate stepping-stone islands. The distributional patterns of the species shared with Dominica and elsewhere in the Caribbean suggest stages in a dynamic taxon cycle of species origin, range expansion, distribution contraction, and re-speciation. Introduction windward (eastern) side (with an average of 250 mm of rain annually). Rainfall is heavy and varies season- The islands of the West Indies are increasingly ally, with the dry season from mid-January to mid- recognized as a hotspot for species biodiversity June and the rainy season from mid-June to mid- (Myers et al. -
(Coleoptera) of Peru Miguel A
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 2-29-2012 Preliminary checklist of the Cerambycidae, Disteniidae, and Vesperidae (Coleoptera) of Peru Miguel A. Monné Universidade Federal do Rio de Janeiro, [email protected] Eugenio H. Nearns University of New Mexico, [email protected] Sarah C. Carbonel Carril Universidad Nacional Mayor de San Marcos, Peru, [email protected] Ian P. Swift California State Collection of Arthropods, [email protected] Marcela L. Monné Universidade Federal do Rio de Janeiro, [email protected] Follow this and additional works at: http://digitalcommons.unl.edu/insectamundi Part of the Entomology Commons Monné, Miguel A.; Nearns, Eugenio H.; Carbonel Carril, Sarah C.; Swift, Ian P.; and Monné, Marcela L., "Preliminary checklist of the Cerambycidae, Disteniidae, and Vesperidae (Coleoptera) of Peru" (2012). Insecta Mundi. Paper 717. http://digitalcommons.unl.edu/insectamundi/717 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. INSECTA MUNDI A Journal of World Insect Systematics 0213 Preliminary checklist of the Cerambycidae, Disteniidae, and Vesperidae (Coleoptera) of Peru Miguel A. Monné Museu Nacional Universidade Federal do Rio de Janeiro Quinta da Boa Vista São Cristóvão, 20940-040 Rio de Janeiro, RJ, Brazil Eugenio H. Nearns Department of Biology Museum of Southwestern Biology University of New Mexico Albuquerque, NM 87131-0001, USA Sarah C. Carbonel Carril Departamento de Entomología Museo de Historia Natural Universidad Nacional Mayor de San Marcos Avenida Arenales 1256, Lima, Peru Ian P. -
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 -
Ant-Like Flower Beetles (Coleoptera: Anthicidae) of the Uk, Ireland and Channel Isles
BR. J. ENT. NAT. HIST., 23: 2010 99 ANT-LIKE FLOWER BEETLES (COLEOPTERA: ANTHICIDAE) OF THE UK, IRELAND AND CHANNEL ISLES DMITRY TELNOV Stopinu novads, Darza iela 10, LV-2130, Dzidrinas, Latvia; E-mail: [email protected] ABSTRACT The Anthicidae or ant-like flower beetles of the UK, Ireland and Channel Isles are reviewed. A species list, identification key, short diagnoses and illustrations of all taxa are given. Brief information on known ecological preferences of species is given. Key words: identification, distribution, key, United Kingdom, Ireland, fauna, ecology. INTRODUCTION Anthicidae are a cosmopolitan family of small to medium-sized, fast-moving beetles of the superfamily Tenebrionoidea. Anthicidae are represented in the World fauna by approximately 100 genera, and about 3500 species (Chandler, 2010). Only a few species are known from the fossil record. The last revision of the British Anthicidae was published by F. D. Buck (1954) in the well-known series Handbooks for the Identification of British Insects. Since then, there have been numerous nomenclatural changes within Anthicidae, and some additional species (introduced) have been recorded from the UK, making Buck’s key out of date. During 2004 and 2005 a total of 3356 specimens of Anthicidae from the UK and Ireland were examined by the author, mainly from the collections of The Natural History Museum (London), Oxford University Museum of Natural History and National Museum of Ireland. Additional data for more than 2100 specimens were received from other British museums and private collections between 2005 and 2007. A new key and short diagnoses for the genera are presented, as well as data on habitats and general distribution of species. -
Redalyc.Escarabajos Coprófagos (Coleoptera: Scarabaeidae
Biota Colombiana ISSN: 0124-5376 [email protected] Instituto de Investigación de Recursos Biológicos "Alexander von Humboldt" Colombia Medina, Claudia A.; Lopera Toro, Alejandro; Vítolo, Adriana; Gill, Bruce Escarabajos Coprófagos (Coleoptera: Scarabaeidae: Scarabaeinae) de Colombia Biota Colombiana, vol. 2, núm. 2, noviembre, 2001, pp. 131- 144 Instituto de Investigación de Recursos Biológicos "Alexander von Humboldt" Bogotá, Colombia Disponible en: http://www.redalyc.org/articulo.oa?id=49120202 Cómo citar el artículo Número completo Sistema de Información Científica Más información del artículo Red de Revistas Científicas de América Latina, el Caribe, España y Portugal Página de la revista en redalyc.org Proyecto académico sin fines de lucro, desarrollado bajo la iniciativa de acceso abierto FernándezBiota Colombiana 2 (2) 131 - 144, 2001 Himenópteros con Aguijón del Neotrópico -131 Escarabajos Coprófagos (Coleoptera: Scarabaeidae: Scarabaeinae) de Colombia Claudia A. Medina1, Alejandro Lopera-Toro2, Adriana Vítolo3 y Bruce Gill4 1 Department of Zoology & Entomology, University of Pretoria, Pretoria 0002 Sur Africa. [email protected] 2 Apartado Aéreo 120118, Bogotá, Colombia. [email protected] 3Instituto de Ciencias Naturales, Universidad Nacional de Colombia - Bogotá. [email protected] 4 Entomology Unit Center for Plant Quarantine Pests Room 4125, K.W. Neatby Bldg. 960 Carling Avenue, Ottawa, Canada K1A0C6. [email protected] Palabras Clave: Escarabajos Coprófagos, Scarabaeidae, Colombia, Lista de Especies, Coleoptera Los escarabajos coprófagos son un gremio bien diversidad de escarabajos coprófagos en zonas de cultivos definido de la familia Scarabaeidae, subfamilia Scarabaeinae, (Camacho 1999), transectos altitudinales (Escobar & que comparten características morfológicas, ecológicas y Valderrama 1995), y efecto de borde (Camacho 1999). Re- de comportamiento particulares (Halffter 1991). -
Victor Michelon Alves EFEITO DO USO DO SOLO NA DIVERSIDADE
Victor Michelon Alves EFEITO DO USO DO SOLO NA DIVERSIDADE E NA MORFOMETRIA DE BESOUROS ESCARABEÍNEOS Tese submetida ao Programa de Pós- Graduação em Ecologia da Universidade Federal de Santa Catarina para a obtenção do Grau de Doutor em Ecologia. Orientadora: Prof.a Dr.a Malva Isabel Medina Hernández Florianópolis 2018 AGRADECIMENTOS À professora Malva Isabel Medina Hernández pela orientação e por todo o auxílio na confecção desta tese. À Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) pela concessão da bolsa de estudos, ao Programa de Pós- graduação em Ecologia da Universidade Federal de Santa Catarina e a todos os docentes por terem contribuído em minha formação científica e acadêmica. Ao professor Paulo Emilio Lovato (CCA/UFSC) pela coordenação do projeto “Fortalecimento das condições de produção e oferta de sementes de milho para a produção orgânica e agroecológica do Sul do Brasil” (CNPq chamada 048/13), o qual financiou meu trabalho de campo. Agradeço imensamente à cooperativa Oestebio e a todos os produtores que permitiram meu trabalho, especialmente aos que me ajudaram em campo: Anderson Munarini, Gleico Mittmann, Maicon Reginatto, Moisés Bacega, Marcelo Agudelo e Maristela Carpintero. Ao professor Jorge Miguel Lobo pela amizade e orientação durante o estágio sanduíche. Ao Museu de Ciências Naturais de Madrid por ter fornecido a infraestrutura necessária para a realização do mesmo. Agradeço também a Eva Cuesta pelo companheirismo e pelas discussões sobre as análises espectrofotométricas. À Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) pela concessão da bolsa de estudos no exterior através do projeto PVE: “Efeito comparado do clima e das mudanças no uso do solo na distribuição espacial de um grupo de insetos indicadores (Coleoptera: Scarabaeinae) na Mata Atlântica” (88881.068089/2014-01).