Check List 9(2): 323–328, 2013 © 2013 Check List and Authors Chec List ISSN 1809-127X (Available at Journal of Species Lists and Distribution
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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 -
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 -
Diversidad De Cantharidae, Lampyridae
Revista Mexicana de Biodiversidad 80: 675- 686, 2009 Diversidad de Cantharidae, Lampyridae, Lycidae, Phengodidae y Telegeusidae (Coleoptera: Elateroidea) en un bosque tropical caducifolio de la sierra de San Javier, Sonora, México Diversity of Cantharidae, Lampyridae, Lycidae, Phengodidae and Telegeusidae (Coleoptera: Elateroidea) in a tropical dry forest of the Sierra San Javier, Sonora, Mexico Santiago Zaragoza-Caballero1* y Enrique Ramírez-García2 1Laboratorio de Entomología, Departamento de Zoología, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 70-153, 04510 México D. F., México. 2Estación de Biología Chamela, Instituto de Biología, Universidad Nacional Autónoma de México. Apartado postal 21, San Patricio 48980 Jalisco, México. *Correspondencia: [email protected] Resumen. Se presenta un estudio de la diversidad faunística de las familias Cantharidae, Lampyridae, Lycidae, Phengodidae y Telegeusidae (Coleoptera: Elateroidea), presentes en un bosque tropical caducifolio de la sierra de San Javier, Sonora, México, que corresponde al límite boreal de este biotopo en América. La recolección incluyó trampas de atracción luminosa y red entomológica aérea, se realizó en noviembre de 2003, febrero y abril de 2004, y de julio a octubre de ese mismo año, durante 5 días de cada mes. Comprende la época lluviosa (julio-octubre) y la temporada seca (noviembre-abril). Se capturó un total de 1 501 individuos que representan 30 especies. La familia más abundante fue Cantharidae con 696 individuos, seguida de Lycidae con 561, Lampyridae con 166, Phengodidae con 66 y Telegeusidae con 12. La más rica en especies fue Lycidae con 12, seguida de Cantharidae con 11, Lampyridae con 3, Phengodidae con 3 y Telegeusidae con 1. -
Insect Classification Standards 2020
RECOMMENDED INSECT CLASSIFICATION FOR UGA ENTOMOLOGY CLASSES (2020) In an effort to standardize the hexapod classification systems being taught to our students by our faculty in multiple courses across three UGA campuses, I recommend that the Entomology Department adopts the basic system presented in the following textbook: Triplehorn, C.A. and N.F. Johnson. 2005. Borror and DeLong’s Introduction to the Study of Insects. 7th ed. Thomson Brooks/Cole, Belmont CA, 864 pp. This book was chosen for a variety of reasons. It is widely used in the U.S. as the textbook for Insect Taxonomy classes, including our class at UGA. It focuses on North American taxa. The authors were cautious, presenting changes only after they have been widely accepted by the taxonomic community. Below is an annotated summary of the T&J (2005) classification. Some of the more familiar taxa above the ordinal level are given in caps. Some of the more important and familiar suborders and families are indented and listed beneath each order. Note that this is neither an exhaustive nor representative list of suborders and families. It was provided simply to clarify which taxa are impacted by some of more important classification changes. Please consult T&J (2005) for information about taxa that are not listed below. Unfortunately, T&J (2005) is now badly outdated with respect to some significant classification changes. Therefore, in the classification standard provided below, some well corroborated and broadly accepted updates have been made to their classification scheme. Feel free to contact me if you have any questions about this classification. -
Conspicuousness, Phylogenetic Structure, and Origins of Müllerian
www.nature.com/scientificreports OPEN Conspicuousness, phylogenetic structure, and origins of Müllerian mimicry in 4000 lycid beetles from all zoogeographic regions Michal Motyka1, Dominik Kusy1, Michal Masek1, Matej Bocek1, Yun Li1, R. Bilkova1, Josef Kapitán2, Takashi Yagi3 & Ladislav Bocak1* Biologists have reported on the chemical defences and the phenetic similarity of net-winged beetles (Coleoptera: Lycidae) and their co-mimics. Nevertheless, our knowledge has remained fragmental, and the evolution of mimetic patterns has not been studied in the phylogenetic context. We illustrate the general appearance of ~ 600 lycid species and ~ 200 co-mimics and their distribution. Further, we assemble the phylogeny using the transcriptomic backbone and ~ 570 species. Using phylogenetic information, we closely scrutinise the relationships among aposematically coloured species, the worldwide diversity, and the distribution of aposematic patterns. The emitted visual signals difer in conspicuousness. The uniform coloured dorsum is ancestral and was followed by the evolution of bicoloured forms. The mottled patterns, i.e. fasciate, striate, punctate, and reticulate, originated later in the course of evolution. The highest number of sympatrically occurring patterns was recovered in New Guinea and the Andean mountain ecosystems (the areas of the highest abundance), and in continental South East Asia (an area of moderate abundance but high in phylogenetic diversity). Consequently, a large number of co-existing aposematic patterns in a single region and/or locality is the rule, in contrast with the theoretical prediction, and predators do not face a simple model-like choice but cope with complex mimetic communities. Lycids display an ancestral aposematic signal even though they sympatrically occur with diferently coloured unproftable relatives. -
Diversity and Abundance of Pest Insects Associated with Solanum Tuberosum L
American Journal of Entomology 2021; 5(3): 51-69 http://www.sciencepublishinggroup.com/j/aje doi: 10.11648/j.aje.20210503.13 ISSN: 2640-0529 (Print); ISSN: 2640-0537 (Online) Diversity and Abundance of Pest Insects Associated with Solanum tuberosum L. 1753 (Solanaceae) in Balessing (West-Cameroon) Babell Ngamaleu-Siewe, Boris Fouelifack-Nintidem, Jeanne Agrippine Yetchom-Fondjo, Basile Moumite Mohamed, Junior Tsekane Sedick, Edith Laure Kenne, Biawa-Miric Kagmegni, * Patrick Steve Tuekam Kowa, Romaine Magloire Fantio, Abdel Kayoum Yomon, Martin Kenne Department of the Biology and Physiology of Animal Organisms, University of Douala, Douala, Cameroon Email address: *Corresponding author To cite this article: Babell Ngamaleu-Siewe, Boris Fouelifack-Nintidem, Jeanne Agrippine Yetchom-Fondjo, Basile Moumite Mohamed, Junior Tsekane Sedick, Edith Laure Kenne, Biawa-Miric Kagmegni, Patrick Steve Tuekam Kowa, Romaine Magloire Fantio, Abdel Kayoum Yomon, Martin Kenne. Diversity and Abundance of Pest Insects Associated with Solanum tuberosum L. 1753 (Solanaceae) in Balessing (West-Cameroon). American Journal of Entomology . Vol. 5, No. 3, 2021, pp. 51-69. doi: 10.11648/j.aje.20210503.13 Received : July 14, 2021; Accepted : August 3, 2021; Published : August 11, 2021 Abstract: Solanum tuberosum L. 1753 (Solanaceae) is widely cultivated for its therapeutic and nutritional qualities. In Cameroon, the production is insufficient to meet the demand in the cities and there is no published data on the diversity of associated pest insects. Ecological surveys were conducted from July to September 2020 in 16 plots of five development stages in Balessing (West- Cameroon). Insects active on the plants were captured and identified and the community structure was characterized. -
Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis
ANRV330-EN53-23 ARI 2 November 2007 18:40 Ancient Rapid Radiations of Insects: Challenges for Phylogenetic Analysis James B. Whitfield1 and Karl M. Kjer2 1Department of Entomology, University of Illinois, Urbana, Illinois 61821; email: jwhitfi[email protected] 2Department of Ecology, Evolution and Natural Resources, Rutgers University, New Brunswick, New Jersey 08901; email: [email protected] Annu. Rev. Entomol. 2008. 53:449–72 Key Words First published online as a Review in Advance on diversification, molecular evolution, Palaeoptera, Orthopteroidea, September 17, 2007 fossils The Annual Review of Entomology is online at ento.annualreviews.org Abstract by UNIVERSITY OF ILLINOIS on 12/18/07. For personal use only. This article’s doi: Phylogenies of major groups of insects based on both morphological 10.1146/annurev.ento.53.103106.093304 and molecular data have sometimes been contentious, often lacking Copyright c 2008 by Annual Reviews. the data to distinguish between alternative views of relationships. Annu. Rev. Entomol. 2008.53:449-472. Downloaded from arjournals.annualreviews.org All rights reserved This paucity of data is often due to real biological and historical 0066-4170/08/0107-0449$20.00 causes, such as shortness of time spans between divergences for evo- lution to occur and long time spans after divergences for subsequent evolutionary changes to obscure the earlier ones. Another reason for difficulty in resolving some of the relationships using molecu- lar data is the limited spectrum of genes so far developed for phy- logeny estimation. For this latter issue, there is cause for current optimism owing to rapid increases in our knowledge of comparative genomics. -
Entomofauna ZEITSCHRIFT FÜR ENTOMOLOGIE
Entomofauna ZEITSCHRIFT FÜR ENTOMOLOGIE Band 36, Heft 40: 529-536 ISSN 0250-4413 Ansfelden, 2. Januar 2015 A study of Coleoptera (Insecta) from the rice fields and surrounding grasslands of northern Iran Hassan GHAHARI , Hamid SAKENIN, Hadi OSTOVAN & Mehrdad TABARI Abstract The fauna of Coleoptera from the rice fields and surrounding grasslands of northern Iran is studied. In total 27 species from 10 families Alleculidae (2), Anthicidae (6), Cantharidae (3), Cleridae (2), Elmidae (3), Glaphyridae (4), Elateridae (3), Helophoridae (2), Silphidae (1), and Spercheidae (1) were collected and identified. Zusammenfassung Die Käferfauna von Reisfeldern und umgebendem Grasland des nördlichen Iran wurde in dieser Arbeit untersucht. Insgesamt konnten 27 Arten der 10 Familien Alleculidae (2), Anthicidae (6), Cantharidae (3), Cleridae (2), Elmidae (3), Glaphyridae (4), Elateridae (3), Helophoridae (2), Silphidae (1), and Spercheidae (1) gesammelt und bestimmt werden. Introduction Coleoptera is the largest order that contains 40% of all described insect species (more than 350,000 species), and new species are constantly discovered. These insects live throughout the world (except Antarctica), but most of them occur in the tropics (WHITE 529 1983; LAWRENCE & BRITTON 1994). The oldest fossils of Coleoptera are from the Lower Permian (about 265 million years ago) (PAKALUK & SLIPINSKI 1995). They range in size from minute featherwing beetles (Ptiliidae, 0.3 mm long) to the giant Goliath and Hercules beetles (Scarabaeidae, over than 15 cm long) (ARNETT 1973; BORROR CORRECT FONT et al. 1989). Beetles have variable life styles, the majority are terrestrial herbivores, though many families are predators, some are parasitic, in both terrestrial and aquatic environments. -
Hox-Logic of Body Plan Innovations for Social Symbiosis in Rove Beetles
bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 Hox-logic of body plan innovations for social symbiosis in rove beetles 2 3 Joseph Parker1*, K. Taro Eldredge2, Isaiah M. Thomas3, Rory Coleman4 and Steven R. Davis5 4 5 1Division of Biology and Biological Engineering, California Institute of Technology, Pasadena, 6 CA 91125, USA 7 2Department of Ecology and Evolutionary Biology, and Division of Entomology, Biodiversity 8 Institute, University of Kansas, Lawrence, KS, USA 9 3Department of Genetics and Development, Columbia University, 701 West 168th Street, New 10 York, NY 10032, USA 11 4Laboratory of Neurophysiology and Behavior, The Rockefeller University, New York, NY 10065, 12 USA 13 5Division of Invertebrate Zoology, American Museum of Natural History, New York, NY 10024, 14 USA 15 *correspondence: [email protected] 16 17 18 19 20 21 22 23 24 25 26 27 1 bioRxiv preprint first posted online Oct. 5, 2017; doi: http://dx.doi.org/10.1101/198945. The copyright holder for this preprint (which was not peer-reviewed) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. All rights reserved. No reuse allowed without permission. 1 How symbiotic lifestyles evolve from free-living ecologies is poorly understood. In 2 Metazoa’s largest family, Staphylinidae (rove beetles), numerous lineages have evolved 3 obligate behavioral symbioses with ants or termites. -
Marine Insects
UC San Diego Scripps Institution of Oceanography Technical Report Title Marine Insects Permalink https://escholarship.org/uc/item/1pm1485b Author Cheng, Lanna Publication Date 1976 eScholarship.org Powered by the California Digital Library University of California Marine Insects Edited by LannaCheng Scripps Institution of Oceanography, University of California, La Jolla, Calif. 92093, U.S.A. NORTH-HOLLANDPUBLISHINGCOMPANAY, AMSTERDAM- OXFORD AMERICANELSEVIERPUBLISHINGCOMPANY , NEWYORK © North-Holland Publishing Company - 1976 All rights reserved. No part of this publication may be reproduced, stored in a retrieval system, or transmitted, in any form or by any means, electronic, mechanical, photocopying, recording or otherwise,without the prior permission of the copyright owner. North-Holland ISBN: 0 7204 0581 5 American Elsevier ISBN: 0444 11213 8 PUBLISHERS: NORTH-HOLLAND PUBLISHING COMPANY - AMSTERDAM NORTH-HOLLAND PUBLISHING COMPANY LTD. - OXFORD SOLEDISTRIBUTORSFORTHEU.S.A.ANDCANADA: AMERICAN ELSEVIER PUBLISHING COMPANY, INC . 52 VANDERBILT AVENUE, NEW YORK, N.Y. 10017 Library of Congress Cataloging in Publication Data Main entry under title: Marine insects. Includes indexes. 1. Insects, Marine. I. Cheng, Lanna. QL463.M25 595.700902 76-17123 ISBN 0-444-11213-8 Preface In a book of this kind, it would be difficult to achieve a uniform treatment for each of the groups of insects discussed. The contents of each chapter generally reflect the special interests of the contributors. Some have presented a detailed taxonomic review of the families concerned; some have referred the readers to standard taxonomic works, in view of the breadth and complexity of the subject concerned, and have concentrated on ecological or physiological aspects; others have chosen to review insects of a specific set of habitats. -
Atlas of Yorkshire Coleoptera (Vcs 61-65)
Atlas of Yorkshire Coleoptera (VCs 61-65) Part 8 - Elateroidea - Families Eucnemidae to Cantharidae Introduction This is Part 8 of the Atlas and covers the Families Eucnemidae, Throscidae, Elateridae, Drilidae, Lycidae, Lampyridae and Cantharidae Each species in the database is considered and in each case a distribution map representing records on the database (at 1/10/2017) is presented. The number of records on the database for each species is given in the account in the form (a,b,c,d,e) where 'a' to 'e' are the number of records from VC61 to VC65 respectively. These figures include undated records (see comment on undated records in the paragraph below on mapping). As a recorder, I shall continue to use the vice-county recording system, as the county is thereby divided up into manageable, roughly equal, areas for recording purposes. For an explanation of the vice-county recording system, under a system devised in Watson (1883) and subsequently documented by Dandy (1969), Britain was divided into convenient recording areas ("vice-counties"). Thus Yorkshire was divided into vice-counties numbered 61 to 65 inclusive, and notwithstanding fairly recent county boundary reorganisations and changes, the vice-county system remains a constant and convenient one for recording purposes; in the text, reference to “Yorkshire” implies VC61 to VC65 ignoring modern boundary changes. For some species there are many records, and for others only one or two. In cases where there are five species or less full details of the known records are given. Many common species have quite a high proportion of recent records. -
A New Fossil Genus of Net-Winged Beetles, with a Brief Review of Amber Lycidae (Insecta: Coleoptera)
Zootaxa 3608 (1): 94–100 ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2013 Magnolia Press ISSN 1175-5334 (online edition) http://dx.doi.org/10.11646/zootaxa.3608.1.8 http://zoobank.org/urn:lsid:zoobank.org:pub:17A52DF2-CD52-44B3-B9F0-CEA906584260 A new fossil genus of net-winged beetles, with a brief review of amber Lycidae (Insecta: Coleoptera) SERGEY V. KAZANTSEV Insect Centre, Donetskaya 13-326, Moscow 109651, Russia. E-mail: [email protected] Abstract A new fossil genus of net-winged beetles, Protolopheros gen. n., and a new species, Protolopheros hoffeinsorum sp. n., are described from the Baltic amber. The new taxon is placed in Erotini, next to Lopheros Leconte, 1881. The extant Pseudaplatopterus (Eropterus) Green, 1951, comb. n. is lowered in rank and placed as a subgenus of the fossil Pseudaplatopterus Kleine, 1940. The extant Kolibaceum (Laterialis) Kazantsev, 1990, comb. n. is lowered in rank and placed as a subgenus of the fossil Kolibaceum Winkler, 1987. Key words: Coleoptera, Lycidae, new genus, new species, taxonomy, Baltic amber, palaeoentomology, Eocene Introduction Although fossil specimens of net-winged beetles (of Dictyoptera sp.) were initially reported from the Baltic amber (Klebs, 1910), the first fossil lycid taxon was described from Florissant Fossil Beds (Upper Eocene/Lower Oligocene) in North America (Wickham, 1914). However, all consequent descriptions were based on amber inclusions, predominantly from the Baltic region. The first Baltic amber lycid taxon, Pseudaplatopterus Kleine, 1940, was presented in the middle of the last century (Kleine, 1940; 1941); afterwards were added another three genera, Hiekeolycus Winkler, 1987, Kolibaceum Winkler, 1987 and Pietrzeniukia Winkler, 1987 (Winkler, 1987).