Indiana 4-H Entomology Insect Flash Cards
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Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Papers in Entomology Museum, University of Nebraska State 12-2009 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson Wichita State University, [email protected] Darcy E. Oishi 2Hawaii Department of Agriculture, Plant Pest Control Branch, Honolulu, [email protected] Brett C. Ratcliffe University of Nebraska-Lincoln, [email protected] Grant T. McQuate USDA-ARS-PBARC, U.S. Pacific Basin Agricultural Research Center, Hilo, HI, [email protected] Follow this and additional works at: https://digitalcommons.unl.edu/entomologypapers Part of the Entomology Commons Jameson, Mary Liz; Oishi, Darcy E.; Ratcliffe, Brett C.; and McQuate, Grant T., "Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii" (2009). Papers in Entomology. 147. https://digitalcommons.unl.edu/entomologypapers/147 This Article is brought to you for free and open access by the Museum, University of Nebraska State at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in Papers in Entomology by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. AProcddition. HawaiianAl inv AEsiventomol scA.r SAocbs. in(2009) HAwA 41:25–30ii 25 Two Additional Invasive Scarabaeoid Beetles (Coleoptera: Scarabaeidae: Dynastinae) in Hawaii Mary Liz Jameson1, Darcy E. Oishi2, Brett C. Ratcliffe3, and Grant T. McQuate4 1Wichita State University, Department of Biological Sciences, 537 Hubbard Hall, Wichita, Kansas 67260 [email protected]; 2Hawaii Department of Agriculture, Plant Pest Control Branch, 1428 South King St., Honolulu, HI 96814 [email protected]; 3University of Nebraska State Museum, Systematics Research Collections, W436 Nebraska Hall, University of Nebraska, Lincoln, Nebraska 68588 [email protected]; 4USDA-ARS-PBARC, U.S. -
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. -
Morphology and Adaptation of Immature Stages of Hemipteran Insects
© 2019 JETIR January 2019, Volume 6, Issue 1 www.jetir.org (ISSN-2349-5162) Morphology and Adaptation of Immature Stages of Hemipteran Insects Devina Seram and Yendrembam K Devi Assistant Professor, School of Agriculture, Lovely Professional University, Phagwara, Punjab Introduction Insect Adaptations An adaptation is an environmental change so an insect can better fit in and have a better chance of living. Insects are modified in many ways according to their environment. Insects can have adapted legs, mouthparts, body shapes, etc. which makes them easier to survive in the environment that they live in and these adaptations also help them get away from predators and other natural enemies. Here are some adaptations in the immature stages of important families of Hemiptera. Hemiptera are hemimetabolous exopterygotes with only egg and nymphal immature stages and are divided into two sub-orders, homoptera and heteroptera. The immature stages of homopteran families include Delphacidae, Fulgoridae, Cercopidae, Cicadidae, Membracidae, Cicadellidae, Psyllidae, Aleyrodidae, Aphididae, Phylloxeridae, Coccidae, Pseudococcidae, Diaspididae and heteropteran families Notonectidae, Corixidae, Belastomatidae, Nepidae, Hydrometridae, Gerridae, Veliidae, Cimicidae, Reduviidae, Pentatomidae, Lygaeidae, Coreidae, Tingitidae, Miridae will be discussed. Homopteran families 1. Delphacidae – Eg. plant hoppers They comprise the largest family of plant hoppers and are characterized by the presence of large, flattened spurs at the apex of their hind tibiae. Eggs are deposited inside plant tissues, elliptical in shape, colourless to whitish. Nymphs are similar in appearance to adults except for size, colour, under- developed wing pads and genitalia. 2. Fulgoridae – Eg. lantern bugs They can be recognized with their antennae inserted on the sides & beneath the eyes. -
A Remarkable Caddisfly with Bipectinate Antennae in Cretaceous
Cretaceous Research 69 (2017) 198e203 Contents lists available at ScienceDirect Cretaceous Research journal homepage: www.elsevier.com/locate/CretRes Short communication A remarkable caddisfly with bipectinate antennae in Cretaceous Burmese amber (Insecta, Trichoptera) * Wilfried Wichard a, Bo Wang b, c, a Institute of Biology, University of Koeln, Gronewaldstr. 2, D 50931 Koeln, Germany b State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, China c Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Science, Beijing 100101, China article info abstract Article history: A new caddisfly (Trichoptera), Palaeopsilotreta xiai gen. et sp. nov. is described based on three well- Received 8 August 2016 preserved male specimens from mid-Cretaceous Burmese amber. It is assigned to the extant family Received in revised form Odontoceridae. Palaeopsilotreta is similar to the extant genus Psilotreta but differs from the latter by 19 September 2016 partially bipectinate antennae which are unknown among living Trichoptera. Our fossils are not only the Accepted in revised form 28 September only Mesozoic Odontoceridae, but also hitherto the earliest record of this family. 2016 © Available online 29 September 2016 2016 Elsevier Ltd. All rights reserved. Keywords: Taxonomy Fossil caddisfly Palaeopsilotreta xiai Psilotreta Odontoceridae 1. Introduction insights into the evolution of this lineage. In this paper, we describe a new extinct genus and species placed in the family Odontocer- Burmese amber (from northern Myanmar) contains the most idae: Palaeopsilotreta xiai gen. et sp. nov., based on three well- diverse biota in amber from the mid-Cretaceous and more than 250 preserved male specimens. -
Aphis Fabae Scop.) to Field Beans ( Vicia Faba L.
ANALYSIS OF THE DAMAGE CAUSED BY THE BLACK BEAN APHID ( APHIS FABAE SCOP.) TO FIELD BEANS ( VICIA FABA L.) BY JESUS ANTONIO SALAZAR, ING. AGR. ( VENEZUELA ) A THESIS SUBMITTED FOR THE DEGREE OF DOCTOR OF PHILOSOPHY IN THE UNIVERSITY OF LONDON OCTOBER 1976 IMPERIAL COLLEGE FIELD STATION, SILWOOD PARK, SUNNINGHILL, ASCOT, BERKSHIRE. 2 ABSTRACT The concept of the economic threshold and its importance in pest management programmes is analysed in Chapter I. The significance of plant responses or compensation in the insect-injury-yield relationship is also discussed. The amount of damage in terms of yield loss that results from aphid attack, is analysed by comparing the different components of yield in infested and uninfested plants. In the former, plants were infested at different stages of plant development. The results showed that seed weights, pod numbers and seed numbers in plants infested before the flowering period were significantly less than in plants infested during or after the period of flower setting. The growth pattern and growth analysis in infested and uninfested plants have shown that the rate of leaf production and dry matter production were also more affected when the infestations occurred at early stages of plant development. When field beans were infested during the flowering period and afterwards, the aphid feeding did not affect the rate of leaf and dry matter production. There is some evidence that the rate of leaf area production may increase following moderate aphid attack during this period. The relationship between timing of aphid migration from the wintering host and the stage of plant development are shown to be of considerable significance in determining the economic threshold for A. -
(Pentatomidae) DISSERTATION Presented
Genome Evolution During Development of Symbiosis in Extracellular Mutualists of Stink Bugs (Pentatomidae) DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Alejandro Otero-Bravo Graduate Program in Evolution, Ecology and Organismal Biology The Ohio State University 2020 Dissertation Committee: Zakee L. Sabree, Advisor Rachelle Adams Norman Johnson Laura Kubatko Copyrighted by Alejandro Otero-Bravo 2020 Abstract Nutritional symbioses between bacteria and insects are prevalent, diverse, and have allowed insects to expand their feeding strategies and niches. It has been well characterized that long-term insect-bacterial mutualisms cause genome reduction resulting in extremely small genomes, some even approaching sizes more similar to organelles than bacteria. While several symbioses have been described, each provides a limited view of a single or few stages of the process of reduction and the minority of these are of extracellular symbionts. This dissertation aims to address the knowledge gap in the genome evolution of extracellular insect symbionts using the stink bug – Pantoea system. Specifically, how do these symbionts genomes evolve and differ from their free- living or intracellular counterparts? In the introduction, we review the literature on extracellular symbionts of stink bugs and explore the characteristics of this system that make it valuable for the study of symbiosis. We find that stink bug symbiont genomes are very valuable for the study of genome evolution due not only to their biphasic lifestyle, but also to the degree of coevolution with their hosts. i In Chapter 1 we investigate one of the traits associated with genome reduction, high mutation rates, for Candidatus ‘Pantoea carbekii’ the symbiont of the economically important pest insect Halyomorpha halys, the brown marmorated stink bug, and evaluate its potential for elucidating host distribution, an analysis which has been successfully used with other intracellular symbionts. -
Predaceous Ground Beetles Caterpillar Hunters and Bombardier
E-185 5-03 PredaceousPredaceous GroundGround BeetBeetlesles Caterpillar Hunters and Bombardier Beetles Rick Minzenmayer, Extension Agent-IPM Chris Sansone, Extension Entomologist Texas Cooperative Extension redaceous ground beetles can be a nui- genus Calosoma, a brightly colored ground sance when numerous. They are beetle. Some species are called “bombardier PPattracted to lights and can sometimes beetles” because they emit what appears to be be found by the hundreds around lights in the smoke from the rear of the abdomen. The morning. The large numbers can also be a “smoke” is actually a glandular fluid that problem because the beetles defend them- vaporizes when it hits air; the fluid can irri- selves by emitting an odor. tate the skin. The ground beetles also emit an Ground beetles are part of the order odor to stop their enemies, including people. Coleoptera. This is the largest order of insects with over a quarter of a million species described throughout the world — about 30,000 species in the United States. Most beetles have two pairs of wings (elytra). The front pair is usually thickened and hard and meet in a straight line down the back when the wings are at rest. The back pair are mem- branous and folded beneath the front pair. All beetles have chewing mouthparts and under- go complete metamorphosis (egg, larva, pupa and adult). Predaceous ground beetles belong to the fami- ly Carabidae. This is the second largest family Caterpillar hunter, Calasoma scrutator (Fabricius) (Coleoptera: of beetles, with more than 2,500 species in Carabidae). North America. Most members of this family are considered beneficial, feeding on other insects in both the larval and adult stages. -
Minutes of the January 25, 2010, Meeting of the Board of Regents
MINUTES OF THE JANUARY 25, 2010, MEETING OF THE BOARD OF REGENTS ATTENDANCE This scheduled meeting of the Board of Regents was held on Monday, January 25, 2010, in the Regents’ Room of the Smithsonian Institution Castle. The meeting included morning, afternoon, and executive sessions. Board Chair Patricia Q. Stonesifer called the meeting to order at 8:31 a.m. Also present were: The Chief Justice 1 Sam Johnson 4 John W. McCarter Jr. Christopher J. Dodd Shirley Ann Jackson David M. Rubenstein France Córdova 2 Robert P. Kogod Roger W. Sant Phillip Frost 3 Doris Matsui Alan G. Spoon 1 Paul Neely, Smithsonian National Board Chair David Silfen, Regents’ Investment Committee Chair 2 Vice President Joseph R. Biden, Senators Thad Cochran and Patrick J. Leahy, and Representative Xavier Becerra were unable to attend the meeting. Also present were: G. Wayne Clough, Secretary John Yahner, Speechwriter to the Secretary Patricia L. Bartlett, Chief of Staff to the Jeffrey P. Minear, Counselor to the Chief Justice Secretary T.A. Hawks, Assistant to Senator Cochran Amy Chen, Chief Investment Officer Colin McGinnis, Assistant to Senator Dodd Virginia B. Clark, Director of External Affairs Kevin McDonald, Assistant to Senator Leahy Barbara Feininger, Senior Writer‐Editor for the Melody Gonzales, Assistant to Congressman Office of the Regents Becerra Grace L. Jaeger, Program Officer for the Office David Heil, Assistant to Congressman Johnson of the Regents Julie Eddy, Assistant to Congresswoman Matsui Richard Kurin, Under Secretary for History, Francisco Dallmeier, Head of the National Art, and Culture Zoological Park’s Center for Conservation John K. -
Mountain Pine Beetle Voltinism and Life History Characteristics Across Latitudinal and Elevational Gradients in the Western United States
For. Sci. 60(3):434–449 FUNDAMENTAL RESEARCH http://dx.doi.org/10.5849/forsci.13-056 entomology & pathology Mountain Pine Beetle Voltinism and Life History Characteristics across Latitudinal and Elevational Gradients in the Western United States Barbara Bentz, James Vandygriff, Camille Jensen, Tom Coleman, Patricia Maloney, Sheri Smith, Amanda Grady, and Greta Schen-Langenheim Substantial genetic variation in development time is known to exist among mountain pine beetle (Dendroctonus ponderosae Hopkins) populations across the western United States. The effect of this variation on geographic patterns in voltinism (generation time) and thermal requirements to produce specific voltinism pathways have not been investigated. The influence of voltinism on fitness traits, body size, and sex ratio is also unclear. We monitored mountain pine beetle voltinism, adult body size, sex ratio, and air temperatures at sites across latitudinal and elevational gradients in the western United States. With the exception of two sites at the coolest and warmest locations, the number of days required to complete a generation was similar. Thermal units required to achieve a generation, however, were significantly less for individuals at the coolest sites. Evolved adaptations explain this pattern, including developmental rates and thresholds that serve to synchronize cohorts and minimize cold-sensitive life stages in winter. These same adaptations reduce the capacity of mountain pine beetle at the warmest sites to take full advantage of increased thermal units, limiting the capacity for bivoltinism within the current realized distribution. Temperature was not correlated with adult size and sex ratio, and size was greatest in host trees other than lodgepole pine (Pinus contorta Dougl.). -
<I>Tibraca Limbativentris</I> (Hemiptera: Pentatomidae)
University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln Faculty Publications: Department of Entomology Entomology, Department of 2018 Resistance in Rice to Tibraca limbativentris (Hemiptera: Pentatomidae) Influenced yb Plant Silicon Content Lincoln Luis França University of Goias State, Unidade Universitária de Ipameri, [email protected] Cássio Antonio Dierings Federal Goiano Institute, Campus Urutaí, Rodovia, [email protected] André Cirilo de Sousa Almeida Federal Goiano Institute, Campus Urutaí, Rodovia, [email protected] Marcio da Silva Araújo University of Goias State, Unidade Universitária de Ipameri Elvis Arden Heinrichs University of Nebraska-Lincoln, [email protected] See next page for additional authors Follow this and additional works at: https://digitalcommons.unl.edu/entomologyfacpub Part of the Agriculture Commons, and the Entomology Commons França, Lincoln Luis; Dierings, Cássio Antonio; de Sousa Almeida, André Cirilo; Araújo, Marcio da Silva; Heinrichs, Elvis Arden; da Silva, Anderson Rodrigo; Freitas Barrigossi, José Alexandre; and de Jesus, Flávio Gonçalves, "Resistance in Rice to Tibraca limbativentris (Hemiptera: Pentatomidae) Influenced yb Plant Silicon Content" (2018). Faculty Publications: Department of Entomology. 900. https://digitalcommons.unl.edu/entomologyfacpub/900 This Article 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 Faculty Publications: -
Zootaxa,Phylogeny and Higher Classification of the Scale Insects
Zootaxa 1668: 413–425 (2007) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ ZOOTAXA Copyright © 2007 · Magnolia Press ISSN 1175-5334 (online edition) Phylogeny and higher classification of the scale insects (Hemiptera: Sternorrhyncha: Coccoidea)* P.J. GULLAN1 AND L.G. COOK2 1Department of Entomology, University of California, One Shields Avenue, Davis, CA 95616, U.S.A. E-mail: [email protected] 2School of Integrative Biology, The University of Queensland, Brisbane, Queensland 4072, Australia. Email: [email protected] *In: Zhang, Z.-Q. & Shear, W.A. (Eds) (2007) Linnaeus Tercentenary: Progress in Invertebrate Taxonomy. Zootaxa, 1668, 1–766. Table of contents Abstract . .413 Introduction . .413 A review of archaeococcoid classification and relationships . 416 A review of neococcoid classification and relationships . .420 Future directions . .421 Acknowledgements . .422 References . .422 Abstract The superfamily Coccoidea contains nearly 8000 species of plant-feeding hemipterans comprising up to 32 families divided traditionally into two informal groups, the archaeococcoids and the neococcoids. The neococcoids form a mono- phyletic group supported by both morphological and genetic data. In contrast, the monophyly of the archaeococcoids is uncertain and the higher level ranks within it have been controversial, particularly since the late Professor Jan Koteja introduced his multi-family classification for scale insects in 1974. Recent phylogenetic studies using molecular and morphological data support the recognition of up to 15 extant families of archaeococcoids, including 11 families for the former Margarodidae sensu lato, vindicating Koteja’s views. Archaeococcoids are represented better in the fossil record than neococcoids, and have an adequate record through the Tertiary and Cretaceous but almost no putative coccoid fos- sils are known from earlier. -
Correlation of Stylet Activities by the Glassy-Winged Sharpshooter, Homalodisca Coagulata (Say), with Electrical Penetration Graph (EPG) Waveforms
ARTICLE IN PRESS Journal of Insect Physiology 52 (2006) 327–337 www.elsevier.com/locate/jinsphys Correlation of stylet activities by the glassy-winged sharpshooter, Homalodisca coagulata (Say), with electrical penetration graph (EPG) waveforms P. Houston Joosta, Elaine A. Backusb,Ã, David Morganc, Fengming Yand aDepartment of Entomology, University of Riverside, Riverside, CA 92521, USA bUSDA-ARS Crop Diseases, Pests and Genetics Research Unit, San Joaquin Valley Agricultural Sciences Center, 9611 South Riverbend Ave, Parlier, CA 93648, USA cCalifornia Department of Food and Agriculture, Mt. Rubidoux Field Station, 4500 Glenwood Dr., Bldg. E, Riverside, CA 92501, USA dCollege of Life Sciences, Peking Univerisity, Beijing, China Received 5 May 2005; received in revised form 29 November 2005; accepted 29 November 2005 Abstract Glassy-winged sharpshooter, Homalodisca coagulata (Say), is an efficient vector of Xylella fastidiosa (Xf), the causal bacterium of Pierce’s disease, and leaf scorch in almond and oleander. Acquisition and inoculation of Xf occur sometime during the process of stylet penetration into the plant. That process is most rigorously studied via electrical penetration graph (EPG) monitoring of insect feeding. This study provides part of the crucial biological meanings that define the waveforms of each new insect species recorded by EPG. By synchronizing AC EPG waveforms with high-magnification video of H. coagulata stylet penetration in artifical diet, we correlated stylet activities with three previously described EPG pathway waveforms, A1, B1 and B2, as well as one ingestion waveform, C. Waveform A1 occured at the beginning of stylet penetration. This waveform was correlated with salivary sheath trunk formation, repetitive stylet movements involving retraction of both maxillary stylets and one mandibular stylet, extension of the stylet fascicle, and the fluttering-like movements of the maxillary stylet tips.