The Trogossitidae (Coleoptera) of Atlantic Canada Christopher G
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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: Cleroidea: Trogossitidae), with a Key to the Palaearctic Species of the Genus
Anim. Syst. Evol. Divers. Vol. 36, No. 2: 139-142, April 2020 https://doi.org/10.5635/ASED.2020.36.2.021 Review article Ancyrona diversa New to Korea (Coleoptera: Cleroidea: Trogossitidae), with a Key to the Palaearctic Species of the Genus Seung-Gyu Lee1, Sang Woo Jung2, Yoon-Ho Kim2,* 1Division of Forest Biodiversity, Korea National Arboretum, Pocheon 11186, Korea 2DASARI Research Institute of BioResources, Daejeon 34127, Korea ABSTRACT The family Trogossitidae Latreille occurs worldwide, including some Pacific islands. The family contains about 50 genera and 600 described species, and the group was recently classified by Kolibáč into three subfamilies, Lophocaterinae, Peltinae and Trogossitinae. Among the lophocaterine genera, a genus Ancyrona Reitter includes 62 species in most parts of the world except the Nearctic region, and is divided into five informal species groups by Kolibáč. In this study, the genus Ancyrona and its a single species, A. diversa (Pic), is newly reported in the Korean fauna. A diagnosis, habitus photographs, and illustrations of female diagnostic characters are provided, with a key to Palaearctic species of the genus Ancyrona. Keywords: Coleoptera, Cleroidea, Trogossitidae, Ancyrona diversa, Korea INTRODUCTION Institute of Biological Resources (NIBR), Incheon, Korea (specimen number EOWQIN0000013458). The genus Ancyrona Reitter, 1876 includes 62 species worldwide (Kolibáč, 2013; Yoshitomi and Asakawa, 2018). In the Palaearctic region, seven species are distributed in Ja- SYSTEMATIC ACCOUNTS pan and one in Russian Far East (Kolibáč, 2013; Yoshitomi and Asakawa, 2018). Up to the present, Ancyrona marginata Order Coleoptera Linnaeus, 1758 is the only species recorded in the Korean Peninsula. Mem- Family Trogossitidae Latreille, 1802 bers of this genus have been known to be collected from dry Subfamily Lophocaterinae Crowson, 1964 branches or on fallen timber, where they hunt for other in- Tribe Ancyronini Kolibáč, 2006 sects (Kolibáč, 2013). -
An Annotated Bibliography of Archaeoentomology
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Distance Master of Science in Entomology Projects Entomology, Department of 4-2020 An Annotated Bibliography of Archaeoentomology Diana Gallagher Follow this and additional works at: https://digitalcommons.unl.edu/entodistmasters Part of the Entomology Commons This Thesis is brought to you for free and open access by the Entomology, Department of at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Distance Master of Science in Entomology Projects by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Diana Gallagher Master’s Project for the M.S. in Entomology An Annotated Bibliography of Archaeoentomology April 2020 Introduction For my Master’s Degree Project, I have undertaken to compile an annotated bibliography of a selection of the current literature on archaeoentomology. While not exhaustive by any means, it is designed to cover the main topics of interest to entomologists and archaeologists working in this odd, dark corner at the intersection of these two disciplines. I have found many obscure works but some publications are not available without a trip to the Royal Society’s library in London or the expenditure of far more funds than I can justify. Still, the goal is to provide in one place, a list, as comprehensive as possible, of the scholarly literature available to a researcher in this area. The main categories are broad but cover the most important subareas of the discipline. Full books are far out-numbered by book chapters and journal articles, although Harry Kenward, well represented here, will be publishing a book in June of 2020 on archaeoentomology. -
The First Mesozoic Palmetto Beetle (Coleoptera: Smicripidae) in Upper
Cretaceous Research 64 (2016) 45e49 Contents lists available at ScienceDirect Cretaceous Research journal homepage: www.elsevier.com/locate/CretRes The first Mesozoic palmetto beetle (Coleoptera: Smicripidae) in Upper Cretaceous Burmese amber * Chenyang Cai a, , Diying Huang b a Key Laboratory of Economic Stratigraphy and Palaeogeography, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China b State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China article info abstract Article history: Fossil smicripid beetles are very rare. Here we describe and figure the first Mesozoic representative of Received 16 January 2016 Smicripidae. Smicrips cretacea sp. nov., a new species belonging to the extant Smicrips LeConte is pre- Received in revised form served in the Upper Cretaceous amber from northern Myanmar. Our discovery suggests that Smicrips is 7 March 2016 an ancient group, originating at least in the earliest Late Cretaceous. Together with other two fossil Accepted in revised form 3 April 2016 Smicrips species from the Eocene of Europe, it reinforces the hypothesis that the Recent distribution of Available online 4 April 2016 Smicripidae is relict, and the family was more widespread in the Mesozoic and early Cenozoic than it is in the Recent. Keywords: © Coleoptera 2016 Elsevier Ltd. All rights reserved. Smicripidae Smicrips Cenomanian Burmese amber 1. Introduction Nitidulidae (Lawrence and Newton, 1995). Members of the Niti- dulidae group (or nitidulid series) including Kateretidae, Smicri- The monogeneric family Smicripidae (or palmetto beetles) is a pidae and Nitidulidae, form a monophyletic group (Leschen et al., small group of small-sized (1.0e1.9 mm long) cucujoid beetles, with 2005). -
The Yearbook of Agriculture • 1961 ^
87TH CONGRESS, IST SESSION, HOUSE DOCUMENT NO. 29 THE YEARBOOK OF AGRICULTURE • 1961 ^ THE UNITED STATES DEPARTMENT OF AGRICULTURE Washington, D.G. SEEDS The Yearbook of Agriculture 1961 ¿^ f i Í THE UNITED STATES GOVERNMENT PRINTING OFFICE FOR SALE BY THE SUPERINTENDENT OF DOCUMENTS, WASHINGTON 25, D.G., PRICE $2 FOREWORD ORVILLE L. FREEMAN Secretary of Agriculture GOOD SEEDS ARE both a symbol and a foundation of the good Ufe our people have gained. A baisic factor in our realization of mankind's most sought goal, agricultural abundance, good seeds can be a means of our bringing about an Age of Plenty and an Age of Peace and Free- dom. We can use our good seeds to help end hunger and fear for the less fortunate half of the human family. So used, our seeds can be more meaningful to a hungry world than can the rocket that first carries man to the moon. This Yearbook of Agriculture seeks to provide a new and improved basis for understanding the complex order of Nature's forces so that man can better shape them in a positive and creative fashion. Seeds are ever a positive and creative force. Seeds are the germ of life, a beginning and an end, the fruit of yesterday's harvest and the promise of tomorrow's. Without an ample store of seeds there can be no national treasure, or no future for a Nation. Finding and developing better seeds is the oldest continuous service our Federal Government has rendered to our farmers—indeed, to all our people. -
STORGARD Insect Identification Poster
® IPM PARTNER® INSECT IDENTIFICATION GUIDE ® Name Photo Size Color Typical Favorite Attracted Geographic Penetrate Product Recommendation (mm) Life Cycle Food to Light Distribution Packages MOTHS Almond Moth 14-20 Gray 25-30 Dried fruit Yes General Yes, Cadra cautella days and grain larvae only STORGARD® II STORGARD® III CIDETRAK® IMM Also available in QUICK-CHANGE™ Also available in QUICK-CHANGE™ (Mating Disruptant) Angoumois 28-35 Yes, Grain Moth 13-17 Buff days Whole grain Yes General larvae only Sitotroga cerealella STORGARD® II STORGARD® III Casemaking 30-60 Wool, natural Yes, Clothes Moth 11 Brownish days fibers and hair Yes General larvae only Tinea pellionella STORGARD® II STORGARD® III European Grain Moth 13-17 White & 90-300 Grain Yes Northern Yes, Nemapogon granellus brown days larvae only STORGARD® II STORGARD® III Copper Indianmeal Moth Broken or 8-10 red & silver 28-35 processed Yes General Yes, Plodia interpunctella days larvae only gray grain STORGARD® II STORGARD® III CIDETRAK® IMM Also available in QUICK-CHANGE™ Also available in QUICK-CHANGE™ (Mating Disruptant) Mediterranean Gray & Flour and Flour Moth 10-15 30-180 processed Yes General Yes, black days larvae only Ephestia kuehniella cereal grain STORGARD® II STORGARD® III CIDETRAK® IMM Also available in QUICK-CHANGE™ Also available in QUICK-CHANGE™ (Mating Disruptant) Raisin Moth Drying and 12-20 Gray 32 days Yes General Yes, dried fruit larvae only Cadra figulilella STORGARD® II STORGARD® III CIDETRAK® IMM Also available in QUICK-CHANGE™ Also available in QUICK-CHANGE™ -
Your Name Here
RELATIONSHIPS BETWEEN DEAD WOOD AND ARTHROPODS IN THE SOUTHEASTERN UNITED STATES by MICHAEL DARRAGH ULYSHEN (Under the Direction of James L. Hanula) ABSTRACT The importance of dead wood to maintaining forest diversity is now widely recognized. However, the habitat associations and sensitivities of many species associated with dead wood remain unknown, making it difficult to develop conservation plans for managed forests. The purpose of this research, conducted on the upper coastal plain of South Carolina, was to better understand the relationships between dead wood and arthropods in the southeastern United States. In a comparison of forest types, more beetle species emerged from logs collected in upland pine-dominated stands than in bottomland hardwood forests. This difference was most pronounced for Quercus nigra L., a species of tree uncommon in upland forests. In a comparison of wood postures, more beetle species emerged from logs than from snags, but a number of species appear to be dependent on snags including several canopy specialists. In a study of saproxylic beetle succession, species richness peaked within the first year of death and declined steadily thereafter. However, a number of species appear to be dependent on highly decayed logs, underscoring the importance of protecting wood at all stages of decay. In a study comparing litter-dwelling arthropod abundance at different distances from dead wood, arthropods were more abundant near dead wood than away from it. In another study, ground- dwelling arthropods and saproxylic beetles were little affected by large-scale manipulations of dead wood in upland pine-dominated forests, possibly due to the suitability of the forests surrounding the plots. -
THE RESPONSE of the CADELLE Tenebroides Mauritanicus (L.) IN
THE RESPONSE OF THE CADELLE Tenebroides mauritanicus (L.) IN THE VACUUM FUMIGATION OF JUTE WITH METHYL BROMIDE by Hector Alexander Urquhart Monro B.S.A. M.Sc. (McGill) A Thesis sutmitted to the Faculty of Graduate Studies and Research of McGill University in partial fulfilment of the requirements for the degree of Doctor of PhilosoPQy. April, 1958. - ii - lm1 PNEUMATICAL ~ERIMENTS ABOUT RESPIRATION XVIII Of Wbat Ha.ppened to Sane Creeping Insects in our Vacuum Notwithstanding the great Variety of Repliills, that Nature does al.most everywhere produce; yet the inconvenient time and place, wherein the following Tryals were made, supplyed me with so few, that about these Animal s I .find among 1liY' Adversaria no more than the ensuing Notes. Experiment I. We took tive or six Ca.terpillars or the same sort; but I could not tell to what ultimate species the Writers about insects reterred them. These being put into a se parable Receiver or a moderate size, bad the Air drawn away !rom them, and caretully kept fran returning. But notwithstanding this deprivatiœ ot Air, I tound them, about an hour atter, moving to and tro in the Receiver; and even above two hours a.tter that, I could by shaking the Vessel, excite in them some motiœs, tbat I did not suspect to be Convulsive. But looking upon them again sane time betore I was to go to bed ( which maybe was about 10 hours arter they were tirst included) they seemed to be quite dead, and, though the Air were forthwith restored to them, they continued to appear so, till I went to Bed; yet, tor Reasons elsewhere expressed, I thought tit to tcy, whether time might not at length recover them, and leaving than all night in the Receiver, I fomd the next day, tbat 3, if not 4 of them, were pertectly alive. -
Ips Bark Beetles and Determining Related Tree Mortality in Arkansas and Texas Chandler Stefan Barton University of Arkansas, Fayetteville
University of Arkansas, Fayetteville ScholarWorks@UARK Theses and Dissertations 5-2015 Monitoring Abundance of Ips Bark Beetles and Determining Related Tree Mortality in Arkansas and Texas Chandler Stefan Barton University of Arkansas, Fayetteville Follow this and additional works at: http://scholarworks.uark.edu/etd Part of the Entomology Commons, and the Forest Sciences Commons Recommended Citation Barton, Chandler Stefan, "Monitoring Abundance of Ips Bark Beetles and Determining Related Tree Mortality in Arkansas and Texas" (2015). Theses and Dissertations. 21. http://scholarworks.uark.edu/etd/21 This Thesis is brought to you for free and open access by ScholarWorks@UARK. It has been accepted for inclusion in Theses and Dissertations by an authorized administrator of ScholarWorks@UARK. For more information, please contact [email protected], [email protected]. Monitoring Abundance of Ips Bark Beetles and Determining Related Tree Mortality in Arkansas and Texas Monitoring Abundance of Ips Bark Beetles and Determining Related Tree Mortality in Arkansas and Texas A thesis submitted in partial fulfillment of the requirements for the degree of Master of Science in Entomology by Chandler Stefan Barton Virginia Polytechnic Institute and State University Bachelor of Science in Forest Resource Management, 2011 May 2015 University of Arkansas This thesis is approved for recommendation to the Graduate Council ____________________________________ Dr. Fred M. Stephen Thesis Director ____________________________________ ____________________________________ Dr. Timothy J. Kring Dr. James M. Guldin Committee Member Committee Member ABSTRACT The abundance of the southern pine engraver beetles, Ips avulsus (Eichhoff), I. grandicollis (Eichhoff), and I. calligraphus (Germar), was monitored with pheromone-baited traps in 2012 and 2013 in Arkansas and eastern Texas. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
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Memoirs of the Museum of Victoria 56(2):659-666 (1997) 28 February 1997 https://doi.org/10.24199/j.mmv.1997.56.67 BIODIVERSITY OF NEW ZEALAND BEETLES (INSECTA, COLEOPTERA) J. KLIMASZEWSK.I Manaaki Whenua — Landcare Research, Private Bag 92170, Auckland, New Zealand Present address: BC Research. 3650 Weshrook Mall, Vancouver V6S SLS, Canada Abstract Klimaszewski, J., 1 997. Biodiversity of New Zealand beetles (Insecta: Coleoptera). Memoirs of the Museum of Victoria 56(2): 659-666. Approximately 5235 species are described for New Zealand, including 354 introduced. They belong to 82 families in two suborders, Adephaga and Polyphaga. The New Zealand beetle fauna is distinguished by the absence of many major lineages, a high level of endem- ism. which in many groups is over 90% at the specific level and over 43% at the generic level (e.g.. Staphylinidae), and the radiation of many groups of genera and species. The origins of New Zealand's beetle fauna are still poorly understood. They are likely to be varied, includ- ing Gondwanan elements and elements which arrived here by short and long-distance dispersal recently and in the remote past. The size of the New Zealand beetle fauna is con- sistent with species number/land area relationships in other areas around the world. Introduction Zealand beetles is that of Kuschel (1990), in the suburb of Lynfield, Auckland, in which 982 The beetles are the largest order of organisms, beetle species were recorded in a diverse veg- with over 350 000 described species world- etation including remnant forest, pastureland, wide. and suburban garden. -
Phylogeny and Classification of Cucujoidea and the Recognition of A
Systematic Entomology (2015), 40, 745–778 DOI: 10.1111/syen.12138 Phylogeny and classification of Cucujoidea and the recognition of a new superfamily Coccinelloidea (Coleoptera: Cucujiformia) JAMES A. ROBERTSON1,2,ADAM SL´ I P I NS´ K I3, MATTHEW MOULTON4, FLOYD W. SHOCKLEY5, ADRIANO GIORGI6, NATHAN P. LORD4, DUANE D. MCKENNA7, WIOLETTA TOMASZEWSKA8, JUANITA FORRESTER9, KELLY B. MILLER10, MICHAEL F. WHITING4 andJOSEPH V. MCHUGH2 1Department of Entomology, University of Arizona, Tucson, AZ, U.S.A., 2Department of Entomology, University of Georgia, Athens, GA, U.S.A., 3Australian National Insect Collection, CSIRO, Canberra, Australia, 4Department of Biology and M. L. Bean Museum, Brigham Young University, Provo, UT, U.S.A., 5Department of Entomology, National Museum of Natural History, Smithsonian Institution, Washington, DC, U.S.A., 6Faculdade de Ciências Biológicas, Universidade Federal do Pará, Altamira, Brasil, 7Department of Biological Sciences, University of Memphis, Memphis, TN, U.S.A., 8Museum and Institute of Zoology, Polish Academy of Sciences, Warszawa, Poland, 9Chattahoochee Technical College, Canton, GA, U.S.A. and 10Department of Biology and Museum of Southwestern Biology, University of New Mexico, Albuquerque, NM, U.S.A. Abstract. A large-scale phylogenetic study is presented for Cucujoidea (Coleoptera), a diverse superfamily of beetles that historically has been taxonomically difficult. This study is the most comprehensive analysis of cucujoid taxa to date, with DNA sequence data sampled from eight genes (four nuclear, four mitochondrial) for 384 coleopteran taxa, including exemplars of 35 (of 37) families and 289 genera of Cucujoidea. Maximum-likelihood analyses of these data present many significant relationships, some proposed previously and some novel.