A Revision of the Coleopterous Family Erotylidae
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Nomenclatural Notes for the Erotylinae (Coleoptera: Erotylidae)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Center for Systematic Entomology, Gainesville, Insecta Mundi Florida 4-29-2020 Nomenclatural notes for the Erotylinae (Coleoptera: Erotylidae) Paul E. Skelley Florida State Collection of Arthropods, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/insectamundi Part of the Ecology and Evolutionary Biology Commons, and the Entomology Commons Skelley, Paul E., "Nomenclatural notes for the Erotylinae (Coleoptera: Erotylidae)" (2020). Insecta Mundi. 1265. https://digitalcommons.unl.edu/insectamundi/1265 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. May 29 2020 INSECTA 35 urn:lsid:zoobank. A Journal of World Insect Systematics org:pub:41CE7E99-A319-4A28- UNDI M B803-39470C169422 0767 Nomenclatural notes for the Erotylinae (Coleoptera: Erotylidae) Paul E. Skelley Florida State Collection of Arthropods Florida Department of Agriculture and Consumer Services 1911 SW 34th Street Gainesville, FL 32608, USA Date of issue: May 29, 2020 CENTER FOR SYSTEMATIC ENTOMOLOGY, INC., Gainesville, FL Paul E. Skelley Nomenclatural notes for the Erotylinae (Coleoptera: Erotylidae) Insecta Mundi 0767: 1–35 ZooBank Registered: urn:lsid:zoobank.org:pub:41CE7E99-A319-4A28-B803-39470C169422 Published in 2020 by Center for Systematic Entomology, Inc. P.O. Box 141874 Gainesville, FL 32614-1874 USA http://centerforsystematicentomology.org/ Insecta Mundi is a journal primarily devoted to insect systematics, but articles can be published on any non- marine arthropod. -
The Distribution and Evolution of Exocrine Compound
This article was downloaded by: [79.238.118.44] On: 17 July 2013, At: 23:24 Publisher: Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Annales de la Société entomologique de France (N.S.): International Journal of Entomology Publication details, including instructions for authors and subscription information: http://www.tandfonline.com/loi/tase20 The distribution and evolution of exocrine compound glands in Erotylinae (Insecta: Coleoptera: Erotylidae) Kai Drilling a b , Konrad Dettner a & Klaus-Dieter Klass b a Department for Animal Ecology II , University of Bayreuth, Universitätsstraße 30 , 95440 , Bayreuth , Germany b Senckenberg Natural History Collections Dresden , Museum of Zoology , Königsbrücker Landstraße 159, 01109 , Dresden , Germany Published online: 24 May 2013. To cite this article: Kai Drilling , Konrad Dettner & Klaus-Dieter Klass (2013) The distribution and evolution of exocrine compound glands in Erotylinae (Insecta: Coleoptera: Erotylidae), Annales de la Société entomologique de France (N.S.): International Journal of Entomology, 49:1, 36-52, DOI: 10.1080/00379271.2013.763458 To link to this article: http://dx.doi.org/10.1080/00379271.2013.763458 PLEASE SCROLL DOWN FOR ARTICLE Taylor & Francis makes every effort to ensure the accuracy of all the information (the “Content”) contained in the publications on our platform. However, Taylor & Francis, our agents, and our licensors make no representations or warranties whatsoever as to the accuracy, completeness, or suitability for any purpose of the Content. Any opinions and views expressed in this publication are the opinions and views of the authors, and are not the views of or endorsed by Taylor & Francis. -
Erotylinae (Insecta: Coleoptera: Cucujoidea: Erotylinae): Taxonomy and Biogeography
EDITORIAL BOARD REPRESENTATIVES OF L ANDCARE RESEARCH Dr D. Choquenot Landcare Research Private Bag 92170, Auckland, New Zealand Dr R. J. B. Hoare Landcare Research Private Bag 92170, Auckland, New Zealand REPRESENTATIVE OF U NIVERSITIES Dr R.M. Emberson c/- Bio-Protection and Ecology Division P.O. Box 84, Lincoln University, New Zealand REPRESENTATIVE OF MUSEUMS Mr R.L. Palma Natural Environment Department Museum of New Zealand Te Papa Tongarewa P.O. Box 467, Wellington, New Zealand REPRESENTATIVE OF O VERSEAS I NSTITUTIONS Dr M. J. Fletcher Director of the Collections NSW Agricultural Scientific Collections Unit Forest Road, Orange NSW 2800, Australia * * * SERIES EDITOR Dr T. K. Crosby Landcare Research Private Bag 92170, Auckland, New Zealand Fauna of New Zealand Ko te Aitanga Pepeke o Aotearoa Number / Nama 59 Erotylinae (Insecta: Coleoptera: Cucujoidea: Erotylidae): taxonomy and biogeography Paul E. Skelley Florida State Collection of Arthropods, Florida Department of Agriculture and Consumer Services, P.O.Box 147100, Gainesville, FL 32614-7100, U.S.A. [email protected] Richard A. B. Leschen Landcare Research, Private Bag 92170, Auckland, New Zealand [email protected] Manaaki W h e n u a PRESS Lincoln, Canterbury, New Zealand 2007 4 Skelley & Leschen (2006): Erotylinae (Insecta: Coleoptera: Cucujoidea: Erotylidae) Copyright © Landcare Research New Zealand Ltd 2007 No part of this work covered by copyright may be reproduced or copied in any form or by any means (graphic, electronic, or mechanical, including photocopying, recording, taping information retrieval systems, or otherwise) without the written permission of the publisher. Cataloguing in publication Skelley, Paul E Erotylinae (Insecta: Coleoptera: Cucujoidea: Erotylidae): taxonomy and biogeography / Paul E. -
Coleoptera: Erotylidae)
Org Divers Evol (2010) 10:205–214 DOI 10.1007/s13127-010-0008-0 ORIGINAL ARTICLE Morphology of the pronotal compound glands in Tritoma bipustulata (Coleoptera: Erotylidae) Kai Drilling & Konrad Dettner & Klaus-Dieter Klass Received: 4 March 2009 /Accepted: 26 November 2009 /Published online: 16 March 2010 # Gesellschaft für Biologische Systematik 2010 Abstract Members of the cucujiform family Erotylidae er Endoplasmatic reticulum possess a whole arsenal of compound integumentary fs Filamentous structure forming core of lateral glands. Structural details of the glands of the pronotum of appendix Tritoma bipustulata and Triplax scutellaris are provided for gd Glandular ductule of gland unit the first time. These glands, which open in the posterior and gdc Constriction of glandular ductule anterior pronotal corners, bear, upon a long, usually gdcl Cell enclosing glandular ductule (secretory cell) unbranched excretory duct, numerous identical gland units, la Lateral appendix of gland unit each comprising a central cuticular canal surrounded by a lacl Cell enclosing lateral appendix (canal cell) proximal canal cell and a distal secretory cell. The canal lu Lumen of glandular ductule or canal cell forms a lateral appendix filled with a filamentous mass m Mitochondrion probably consisting of cuticle, and the cuticle inside the mgdcl Membrane of cell enclosing glandular ductule secretory cell is strongly spongiose—both structural fea- mlacl Membrane of cell enclosing lateral appendix tures previously not known for compound glands of beetles. ngc Non-glandular cell Additional data are provided for compound glands of the rw Ringwall around orifice of glandular ductule prosternal process and for simple (dermal) glands of the ss Spongiose structure of cuticular intima of pronotum. -
Status and Development of Old-Growth Elements and Biodiversity During Secondary Succession of Unmanaged Temperate Forests
Status and development of old-growth elementsand biodiversity of old-growth and development Status during secondary succession of unmanaged temperate forests temperate unmanaged of succession secondary during Status and development of old-growth elements and biodiversity during secondary succession of unmanaged temperate forests Kris Vandekerkhove RESEARCH INSTITUTE NATURE AND FOREST Herman Teirlinckgebouw Havenlaan 88 bus 73 1000 Brussel RESEARCH INSTITUTE INBO.be NATURE AND FOREST Doctoraat KrisVDK.indd 1 29/08/2019 13:59 Auteurs: Vandekerkhove Kris Promotor: Prof. dr. ir. Kris Verheyen, Universiteit Gent, Faculteit Bio-ingenieurswetenschappen, Vakgroep Omgeving, Labo voor Bos en Natuur (ForNaLab) Uitgever: Instituut voor Natuur- en Bosonderzoek Herman Teirlinckgebouw Havenlaan 88 bus 73 1000 Brussel Het INBO is het onafhankelijk onderzoeksinstituut van de Vlaamse overheid dat via toegepast wetenschappelijk onderzoek, data- en kennisontsluiting het biodiversiteits-beleid en -beheer onderbouwt en evalueert. e-mail: [email protected] Wijze van citeren: Vandekerkhove, K. (2019). Status and development of old-growth elements and biodiversity during secondary succession of unmanaged temperate forests. Doctoraatsscriptie 2019(1). Instituut voor Natuur- en Bosonderzoek, Brussel. D/2019/3241/257 Doctoraatsscriptie 2019(1). ISBN: 978-90-403-0407-1 DOI: doi.org/10.21436/inbot.16854921 Verantwoordelijke uitgever: Maurice Hoffmann Foto cover: Grote hoeveelheden zwaar dood hout en monumentale bomen in het bosreservaat Joseph Zwaenepoel -
Insects and Related Arthropods Associated with of Agriculture
USDA United States Department Insects and Related Arthropods Associated with of Agriculture Forest Service Greenleaf Manzanita in Montane Chaparral Pacific Southwest Communities of Northeastern California Research Station General Technical Report Michael A. Valenti George T. Ferrell Alan A. Berryman PSW-GTR- 167 Publisher: Pacific Southwest Research Station Albany, California Forest Service Mailing address: U.S. Department of Agriculture PO Box 245, Berkeley CA 9470 1 -0245 Abstract Valenti, Michael A.; Ferrell, George T.; Berryman, Alan A. 1997. Insects and related arthropods associated with greenleaf manzanita in montane chaparral communities of northeastern California. Gen. Tech. Rep. PSW-GTR-167. Albany, CA: Pacific Southwest Research Station, Forest Service, U.S. Dept. Agriculture; 26 p. September 1997 Specimens representing 19 orders and 169 arthropod families (mostly insects) were collected from greenleaf manzanita brushfields in northeastern California and identified to species whenever possible. More than500 taxa below the family level wereinventoried, and each listing includes relative frequency of encounter, life stages collected, and dominant role in the greenleaf manzanita community. Specific host relationships are included for some predators and parasitoids. Herbivores, predators, and parasitoids comprised the majority (80 percent) of identified insects and related taxa. Retrieval Terms: Arctostaphylos patula, arthropods, California, insects, manzanita The Authors Michael A. Valenti is Forest Health Specialist, Delaware Department of Agriculture, 2320 S. DuPont Hwy, Dover, DE 19901-5515. George T. Ferrell is a retired Research Entomologist, Pacific Southwest Research Station, 2400 Washington Ave., Redding, CA 96001. Alan A. Berryman is Professor of Entomology, Washington State University, Pullman, WA 99164-6382. All photographs were taken by Michael A. Valenti, except for Figure 2, which was taken by Amy H. -
Curriculum Vitae
CURRICULUM VITAE Christopher E. Carlton Department of Entomology, LSU AgCenter Baton Rouge, LA 70803-1710 e-mail: [email protected] EDUCATION Bachelor of Science, Biology, 1977, Hendrix College, Conway, Arkansas. Master’s Degree, Entomology, 1983, University of Arkansas, Fayetteville. Doctor of Philosophy, Entomology, 1989, University of Arkansas, Fayetteville. HISTORY OF ASSIGNMENTS Louisiana State University, Baton Rouge 1995-2000, Assistant Professor; 2000-2005, Associate Professor; 2005-2007, Professor, 2007-present, John Benjamin Holton Alumni Association Departmental Professorship in Agriculture, Department of Entomology. Research in insect systematics, Director, Louisiana State Arthropod Museum, teach systematics and general entomology courses and direct graduate training programs. University of Arkansas, Fayetteville 1989-1995: Research Associate, Department of Entomology. Conduct research in biodiversity and systematics, provide identifications of insects and diagnoses of related problems, and curate University of Arkansas Arthropod Museum. 1982-1989: Research Assistant (degree track), Department of Entomology. Manage entomology collection and provide insect identifications. 1977-1981: Graduate Assistant, Department of Entomology. Graduate student in Master's Program. TEACHING Courses Taught and LSU SPOT Scores ENTM 7001 General Entomology, co-instructed with Jim Ottea, 4 credit hours Provides a framework of information about the evolution of insects and related arthropods, anatomy, functional morphology and physiology, and an introduction to insect diversity at the ordinal level. This course replaced 7014. Fall 2006 Total 4.07 (College Stats 4.03); n=3 Fall 2008 Total 4.22 (College Stats 4.07); n=12 Fall 2010 Total 3.89 (College Stats 4.15); n=11 Fall 2012 Spots not available; n=12 ENTM 4005 Insect Taxonomy, 4 credit hours This course teaches basic principles of taxonomy and nomenclature. -
The Pleasing Fungus Beetles of Illinois (Coleoptera: Erotylidae) Part II
Transactions of the Illinois State Academy of Science (1993), Volume 86, 3 and 4, pp. 153 - 171 The Pleasing Fungus Beetles of Illinois (Coleoptera: Erotylidae) Part II. Triplacinae. Triplax and Ischyrus Michael A. Goodrich Department of Zoology, Eastern Illinois University Charleston, IL 61920, U.S.A. and Paul E. Skelley Entomology and Nematology Department University of Florida, Gainesville, FL 32611, U.S.A. ABSTRACT The Illinois fauna of the subfamily Triplacinae (Coleoptera: Erotylidae) includes 3 known genera: Triplax Herbst, Ischyrus Lacordaire and Tritoma Fabricius. The eight species of Triplax and the single species of Ischyrus known to occur in Illinois are treated in this paper. Three new records for Illinois are reported: Triplax macra LeConte; Triplax festiva Lacordaire; and Triplax puncticeps Casey. Keys to the identification of adults, descriptions of each species, habitus drawings and distribution maps are provided. Fungal host relationships of each species are reported and discussed. The family Erotylidae includes colorful fungus feeding beetles commonly called "pleasing fungus beetles". They are world wide in distribution with over 2000 described species. The family was comprehensively revised for North America by Boyle in 1956. Of the 44 genera reported from the New World (Blackwelder 1945; Boyle 1956); 10 genera and 49 species are known north of Mexico (Boyle 1956, 1962; Goodrich & Skelley 1991a). Within the subfamily Triplacinae, 6 genera and 40 species occur nationally. The purpose of this series of papers is to provide a complete list of the Erotylidae occurring in Illinois, keys and descriptions of adults of each species for identification, distribution maps of their occurrence within the state, and descriptions of their biology and host relationships. -
Pest Complex of Cultivated Oyster Mushroom in Northeast India: Feeding Losses and Role of Micro-Climate in Pest Multiplication
Content list available at http://epubs.icar.org.in, www.kiran.nic.in; ISSN: 0970-6429 Indian Journal of Hill Farming December 2017, Volume 30, Issue 2, Page 259-267 Pest Complex of Cultivated Oyster Mushroom in Northeast India: Feeding Losses and Role of Micro-climate in Pest Multiplication B. Nongkynrih* . D.M. Firake . P. Baiswar . G.T. Behere . S. Chandra . S. V. Ngachan Division of Crop Protection, ICAR Research Complex for NEH Region, Umroi road, Umiam-793103, Meghalaya ARTICLE INFO ABSTRACT Article history: The northeast India is one of the most promising regions for the cultivation of mushroom; Received 3 January 2017 where oyster mushroom is a widely accepted and popular food among the local people. Revision Received 25 June 2017 Accepted 15 August 2017 Despite higher demand, the year-round production of oyster mushroom is usually not ----------------------------------------------- possible, which is mainly due to severe damage by the insect pests and diseases, especially Key words: Mycetophagus insect, Pleasing fungus during rainy season. We studied the detailed pest complex of oyster mushroom, their beetle, Sciarid fly, Rove beetle, damage pattern and the role of micro-climatic factors on pest multiplication during 2013 Collembola and 2014. Various arthropod pests viz., pleasing fungus beetles (Triplax spp., Scaphisoma ---------------------------------------------- spp. and Megalodacne spp.) sciarid fly (Bradysia spp.), mycetophilid fly (Allactoneura spp.), fruit fly (Drosophila spp.), rove beetles, noctuid moths, collembolans and mites (Tyrophagus spp.) were found infesting oyster mushroom in different months of the year. Pest incidence was found upto 100% during the rainy season (May, June, July and August). Among all, Triplax spp. -
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. -
Beetles of Eoa Genus Species
BEETLES OF EOA GENUS SPECIES Acamaeodera tubulus Acanthoscealis obsoletus Acanthoscelides sp. Agonum sp. Agrilus egenus Agrilus politus Alobates pennsylvanica Amara sp. Ampedus nigricans Analeptura lineola Anisostena nigrita Anomoea laticlavia Anthaxia inornata Anthicus sp. Anthocomus ulkei ? Anthonomus suturalis Aphodius stercorosus Apion decoloratum Apion patruele Apion rostrum Arrhenodes minutus Babia quadriguttata Baliosus nervosus Bembidion fugax Berosus ordinatus Bidessonotus inconspicuus Blapstinus moestus Blepherida rhois Brachiacantha felina Brachiacantha quadripunctata Brachypnoea puncticollis Brachys ovatus Bradycellus neglectus Calligrapha bidenticola Calopteron terminale Calosoma scrutator Cantharis bilineatus Cantharis dentiger Cantharis fraxini Cantharis impressus Cantharis rectus Cantharis scitulus Canthon Hudsonias Capraita sexmaculata Capraita subvittata Cassida rubiginosa Cerotoma trifurcata Cercyon praetextatus Ceutorhynchus sp. Chaetocnema irregularis Chaetocnema pulicaria Chaetocnema sp. Charidotella sexpunctata bicolor Charidotella sexpunctata Chauliognathus marginatus Chauliognathus pennsylvanicus Chelymorpha cassidea Chlaenius aestivuus Chrysobotheris harrisi Chrysochus auratus Chrysomela interrupta Chrysomela scripta Cicindela repanda Cicindela punctulata Cicindela duodecimguttata Cicindela splendida Cicindela sexguttata Coccinella septempunctata Coleomegilla maculata lengi Colliuris pennsylvanicus Coloemegilla maculata Copris tullius Crepidodera longula Crepidodera nana Crepidodera violacea Cryptocephalus binominus -
Metamorphosis Is Induced by Food Absence Rather Than a Critical Weight in the Solitary Bee, Osmia Lignaria
Metamorphosis is induced by food absence rather than a critical weight in the solitary bee, Osmia lignaria Bryan R. Helma,1, Joseph P. Rinehartb, George D. Yocumb, Kendra J. Greenleea, and Julia H. Bowshera aDepartment of Biological Sciences, North Dakota State University, Fargo, ND 58108-6050; and bAgricultural Research Service–Insect Genetics and Biochemistry, Red River Valley Agricultural Research Center, United States Department of Agriculture, Fargo, ND 58102 Edited by Lynn M. Riddiford, University of Washington, Friday Harbor, WA, and approved August 22, 2017 (received for review February 21, 2017) Body size is an important phenotypic trait that correlates with these factors explains adult body size variation in Manduca sexta performance and fitness. For determinate growing insects, body size and Drosophila melanogaster, including variation in response to variation is determined by growth rate and the mechanisms that stop different environmental conditions (21–23) and selection under growth at the end of juvenile growth. Endocrine mechanisms laboratory conditions (24–26). Of the three factors, the critical regulate growth cessation, and their relative timing along develop- weight is the most important, representing the decision to commit ment shapes phenotypic variation in body size and development to metamorphosis (8, 19, 20), and is thus a central component of time. Larval insects are generally hypothesized to initiate meta- understanding size variation. morphosis once they attain a critical weight. However, the mecha- The intrinsic or extrinsic cues that larvae use to sense that they nisms underlying the critical weight have not been resolved even for have reached the critical weight remain unresolved. Seminal well-studied insect species.