45972003 GRI Annual Report
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Beetle Chrysomela Populi
Tissue-Specific Transcript Profiling for ABC Transporters in the Sequestering Larvae of the Phytophagous Leaf Beetle Chrysomela populi Anja S. Strauss1., Ding Wang1., Magdalena Stock1., Rene´ R. Gretscher1, Marco Groth2, Wilhelm Boland1, Antje Burse1* 1 Max Planck Institute for Chemical Ecology, Beutenberg Campus, Hans-Knoell-Str. 8, D-07745 Jena, Thuringia, Germany, 2 Leibniz Institute for Age Research – Fritz Lipmann Institute, Beutenbergstr. 11, D-07745 Jena, Thuringia, Germany Abstract Background: Insects evolved ingenious adaptations to use extraordinary food sources. Particularly, the diet of herbivores enriched with noxious plant secondary metabolites requires detoxification mechanisms. Sequestration, which involves the uptake, transfer, and concentration of occasionally modified phytochemicals into specialized tissues or hemolymph, is one of the most successful detoxification strategies found in most insect orders. Due to the ability of ATP-binding cassette (ABC) carriers to transport a wide range of molecules including phytochemicals and xenobiotics, it is highly likely that they play a role in this sequestration process. To shed light on the role of ABC proteins in sequestration, we describe an inventory of putative ABC transporters in various tissues in the sequestering juvenile poplar leaf beetle, Chrysomela populi. Results: In the transcriptome of C. populi, we predicted 65 ABC transporters. To link the proteins with a possible function, we performed comparative phylogenetic analyses with ABC transporters of other insects and of humans. While tissue- specific profiling of each ABC transporter subfamily suggests that ABCB, C and G influence the plant metabolite absorption in the gut, ABCC with 14 members is the preferred subfamily responsible for the excretion of these metabolites via Malpighian tubules. -
Conservation Biological Control Using Selective Insecticides – a Valuable Tool for IPM T ⁎ Jorge B
Biological Control 126 (2018) 53–64 Contents lists available at ScienceDirect Biological Control journal homepage: www.elsevier.com/locate/ybcon Conservation biological control using selective insecticides – A valuable tool for IPM T ⁎ Jorge B. Torresa, , Adeney de F. Buenob a Departamento de Agronomia/Entomologia, Universidade Federal Rural de Pernambuco, Rua Dom Manoel de Medeiros s/n, Dois Irmãos, Recife, PE 52171-900, Brazil b Embrapa Soja, Caixa Postal 231, Londrina, PR 86001-970, Brazil ARTICLE INFO ABSTRACT Keywords: Conservation biological control (CBC) has widely benefited from ecological practices that enhance both the crop Nontarget and its surrounding environment. However, use of insecticides, whether biological or synthetic compounds, is Pesticide often detrimental to natural enemies. By definition toxic to insects, insecticides may cause direct mortality of Physiological selectivity natural enemies, reduce food resources (prey/host), or disrupt behavioral and biological processes. Therefore, Ecological selectivity choosing a selective insecticide or selectively applying are important decisions for conserving natural enemies if Soybean insecticide is required. In situations where both insecticide and natural enemy do not share the same target pest, Cotton an additive outcome is expected and CBC can minimize pest outbreaks and resurgence. Given that new, selective insecticides are usually more expensive than older ones, using the former typically adds cost per treated area. Therefore, choosing a selective insecticide becomes a matter of benefits and costs, considering the cost compared to other available treatments and potential pest problems. Beyond the differential toxicity of selective in- secticides to natural enemy and target pest species, some human decisions may produce insecticide selectivity, including application of minimal effective rates, and spatiotemporal separation of nonselective insecticides and natural enemies. -
Notes on the Natural History of Juneau, Alaska
Notes on the Natural History of Juneau, Alaska Observations of an Eclectic Naturalist Volume 2 Animals L. Scott Ranger Working version of Jul. 8, 2020 A Natural History of Juneau, working version of Jul. 8, 2020 Juneau Digital Shaded-Relief Image of Alaska-USGS I-2585, In the Public Domain Natural History of Juneau, working version of Jul. 8, 2020 B Notes on the Natural History of Juneau, Alaska Observations of an Eclectic Naturalist Volume 2: Animals L. Scott Ranger www.scottranger.com, [email protected] Production Notes This is very much a work under construction. My notes are composed in Adobe InDesign which allows incredible precision of all the elements of page layout. My choice of typefaces is very specific. Each must include a complete set of glyphs and extended characters. For my etymologies the font must include an easily recognized Greek and the occasional Cyrillic and Hebrew. All must be legible and easily read at 10 points. Adobe Garamond Premier Pro is my specifically chosen text typeface. I find this Robert Slimbach 1989 revision of a typeface created by Claude Garamond (c. 1480–1561) to be at once fresh and classic. Long recognized as one of the more legible typefaces, I find it very easy on the eye at the 10 point size used here. I simply adore the open bowls of the lower case letters and find the very small counters of my preferred two- storied “a” and the “e” against its very open bowl elegant. Garamond’s ascenders and decenders are especially long and help define the lower case letters with instant recognition. -
IBMB 2009 1.Pdf
Pyrosequencing of the midgut transcriptome of the poplar leaf beetle Chrysomela tremulae reveals new gene families in Coleoptera Yannick Pauchet, Paul Wilkinson, Manuella van Munster, Sylvie Augustin, David Pauron, Richard Ffrench-Constant To cite this version: Yannick Pauchet, Paul Wilkinson, Manuella van Munster, Sylvie Augustin, David Pauron, et al.. Pyrosequencing of the midgut transcriptome of the poplar leaf beetle Chrysomela tremulae reveals new gene families in Coleoptera. Insect Biochemistry and Molecular Biology, Elsevier, 2009, 39 (5-6), pp.403-413. 10.1016/j.ibmb.2009.04.001. hal-02668241 HAL Id: hal-02668241 https://hal.inrae.fr/hal-02668241 Submitted on 31 May 2020 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. ARTICLE IN PRESS IB2039_proof 16 April 2009 1/11 Insect Biochemistry and Molecular Biology xxx (2009) 1–11 Contents lists available at ScienceDirect Insect Biochemistry and Molecular Biology journal homepage: www.elsevier.com/locate/ibmb 55 1 56 2 Pyrosequencing of the midgut transcriptome of the poplar leaf beetle 57 3 58 4 Chrysomela tremulae reveals new gene families in Coleoptera 59 5 60 6 Yannick Pauchet a,*, Paul Wilkinson a, Manuella van Munster b, Sylvie Augustin c, 61 62 7 David Pauron b, Richard H. -
Cottonwood Leaf Beetle Control with Imidacloprid Soaked Cuttings Terry L
Cottonwood LEAF BEETLE CONTROL WITH IMIDACLOPRID SOAKED CUTTINGS Terry L. Robison and Randall J. Rousseau1 Abstract—Dormant, unrooted cuttings from three eastern cottonwood (Populus deltoides Marsh.) clones were soaked in either water or one of two concentrations of dmire® 2 Flowable (imidacloprid) insecticide. Half were planted immediately after soaking while the other half were stored for 12 weeks at -2°C prior to planting. Trees from cuttings soaked in either the 0.053 or 0.106 percent imidacloprid solutions were significantly taller at each measurement date and had lower levels of insect feeding than trees from cuttings soaked in water. Insect feeding on shoot terminals was limited almost entirely to the control trees (water soaked). Treatment effects lasted for over 14 weeks, but insect population levels were low at the end of the growing season limiting damage. In a related observational study, imidacloprid treatment effects seemed to carry into June of the second growing season. INTRODUCTION Cottonwood leaf beetle (Chrysomela scripta F.) is a major defoliator of Populus plantations (brahamson and others 1977, urkot and enjamin 1979, Coyle and others 2005) with preferred clones containing parentage from the igeiros or Tacamahaca sections (Caldbeck and others 1978, Harrell and others 1981, ingaman and Hart 1992). oth cottonwood leaf beetle (CL) adults and larvae feed on young leaves, with larvae causing the most damage. When population numbers are high, larvae may completely consume young leaves and shoot tips. ecause CL have up to five generations per year (Coyle and others 2005), high population levels can be attained quickly under favorable conditions (ingaman and Hart 1992) such as warm, extended growing seasons (Mattson and others 2001). -
Cottonwood Leaf Beetle, Chrysomela Scripta Fabricius
Colorado Insects of Interest Knab's Willow Leaf Beetle/ Cottonwood Leaf Beetle Scientific Names: Knab's willow leaf beetle, Chrysomela knabi (Linneaus); cottonwood leaf beetle, Chrysomela scripta Fabricius Order: Coleoptera (Beetles) Family: Chrysomelidae (Leaf Beetles) Identification and Descriptive Features: Figure 1. Cottonwood leaf beetle (left) and Knab's Knab's willow leaf beetle adults somewhat willow leaf beetles (right, above) feeding on peachleaf resemble a large lady beetle. There can have willow. a range of color with most being red or red- dish orange, but yellow and light brown forms also occur. They are spotted with black markings, which can be highly variable in number and prominence (Fig. 1). Knab's willow leaf beetle is most commonly associated with certain willows (e.g., peachleaf) but also may feed on aspens. Adults of cottonwood leaf beetle show a similar range in size. They can be differentiated by having dark markings that are more elongated and the overall coloration is normally light gray or brown, never red (Fig. 1). Plains cottonwood is the most common host of this species, but it feeds on some other Populus and may co-occur with Knab's willow leaf beetle on some willows (Salix). Immature stages of both insects are generally similar in appearance. Eggs are yellow and laid in loose clusters on the underside of leaves; the eggs somewhat resemble those of lady beetles but are brighter yellow and more widely space within a cluster. Early stage larvae are black and somewhat resemble lady beetle larvae, but move very slowly and feed on leaves. Older larvae have some white markings (Fig. -
Cottonwood Leaf Beetlechrysomela Scripta
Archival copy: for current recommendations see http://edis.ifas.ufl.edu or your local extension office. EENY-519 Cottonwood Leaf Beetle Chrysomela scripta Fabricius (Insecta: Coleoptera: Chrysomelidae: Chrysomela) 1 Amelio A. Chi and Russell F. Mizell III2 Introduction cause extensive leaf loss, and can consequently reduce stem volume up to 70% (Coyle et al. 2005). The cottonwood leaf beetle, Chrysomela scripta Fabricius, is one of the most economically-important pests of managed Cottonwood, Populus deltoides, is its primary host. As soon cottonwood, aspen, and some poplar and willow species. as spring leaf growth occurs, the cottonwood leaf beetle Although it does not present a serious pest problem in moves from under the bark, litter, or forest debris to the forests, often it is a severe pest of urban ornamental trees. host trees to feed on the leaves and twigs. The beetle feeds This leaf feeder has several generations each year, may most often on immature buds. Leaf beetles can complete Figure 1. Adult (upper left) and various larval instars of the Figure 2. Adult cottonwood leaf beetle, Chrysomela scripta Fabricius, cottonwood leaf beetle, Chrysomela scripta Fabricius, feeding on feeding on foliage. foliage. Credits: Lacy Hyche, Auburn University; www.insectimages.org Credits: Lacy Hyche, Auburn University; www.insectimages.org 1. This document is EENY-519, one of a series of the Entomology and Nematology Department, Florida Cooperative Extension Service, Institute of Food and Agricultural Sciences, University of Florida. Original publication date June 2012. Visit the EDIS website at http://edis.ifas.u..edu. 2. Amelio A. Chi, Entomology and Nematology Department; and Russell F. -
Relationship Between Poplar Leaf Chemicals and Cottonwood Leaf Beetle Adult Feeding Preferences Sisi Lin Iowa State University
Iowa State University Capstones, Theses and Retrospective Theses and Dissertations Dissertations 1997 Relationship between poplar leaf chemicals and cottonwood leaf beetle adult feeding preferences Sisi Lin Iowa State University Follow this and additional works at: https://lib.dr.iastate.edu/rtd Part of the Ecology and Evolutionary Biology Commons, Entomology Commons, and the Environmental Sciences Commons Recommended Citation Lin, Sisi, "Relationship between poplar leaf chemicals and cottonwood leaf beetle adult feeding preferences " (1997). Retrospective Theses and Dissertations. 11483. https://lib.dr.iastate.edu/rtd/11483 This Dissertation is brought to you for free and open access by the Iowa State University Capstones, Theses and Dissertations at Iowa State University Digital Repository. It has been accepted for inclusion in Retrospective Theses and Dissertations by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. INFORMATION TO USERS This manuscript has been reproduced from the microfilm master. TJMI films the text directly fi'om the original or copy submitted. Thus, some thesis and dissertation copies are in typewriter &ce, while others may be fi'om any type of computer printer. The quality of this reproduction is dependent upon the quality of the copy submitted. Broken or indistinct print, colored or poor quality illustrations and photographs, print bleedthrough, substandard margins, and improper alignment can adversely affect reproduction. In the unlikely event that the author did not send UMI a complete manuscript and there are missing pages, these will be noted. Also, if unauthorized copyright material had to be removed, a note will indicate the deletion. Oversize materials (e.g., maps, drawings, charts) are reproduced by sectioning the original, beginning at the upper left-hand comer and continuing fi'om left to right in equal sections with small overlaps. -
Sequestration in Leaf Beetles
Sequestration in leaf beetles: Identification and characterization of ABC transporters involved in the chemical defense of Chrysomelina larvae Dissertation zur Erlangung des akademischen Grades „doctor rerum naturalium“ (Dr. rer. nat.) vorgelegt dem Rat der Biologisch-Pharmazeutischen Fakultät der Friedrich-Schiller-Universität Jena Anja S. Strauß (Diplom-Biochemikerin) geboren am 24.12.1979 in Gera 24. Januar 2014 Gutachter: 1. Prof. Dr. Wilhelm Boland, Max-Planck-Institut für Chemische Ökologie, Jena 2. Prof. Dr. Stefan Heinemann, Friedrich-Schiller-Universität Jena 3. Prof. Dr. Monika Hilker, Freie Universität Berlin Tag der öffentlichen Verteidigung: 1. Juli 2014 Anmerkung Die nachfolgend dokumentierten Arbeiten wurden am Max-Planck-Institut für chemi- sche Ökologie Jena in der Arbeitsgruppe für Bioorganische Chemie unter der Leitung von Prof. Dr. Wilhelm Boland angefertigt. Meinen Eltern Contents 1 Introduction 1 1.1 Plant-herbivore interactions . 1 1.2 Sequestration is widely distributed in insects . 2 1.3 Sequestration and chemical defense of leaf beetle larvae . 3 1.3.1 Defensive glands of Chrysomelina larvae . 4 1.3.2 Chemical defense of Chrysomelina larvae . 5 1.3.3 Host plant adaptation within the Chrysomelina subtribe . 6 1.4 An introduction to the investigated species . 6 1.4.1 Chrysomela populi - life cycle and occurence . 7 1.5 Transport of glucosides in Chrysomelina larvae . 8 1.5.1 Transport processes across membranes . 8 1.5.2 Transport network for plant glucosides in Chrysomelina larvae . 9 1.5.3 ABC transporter as putative transport proteins involved in the sequestration of Chrysomelina larvae . 11 2 Overview of manuscripts 13 3 Manuscripts 16 I “Always being well prepared for defense: The production of deterrents by juvenile Chrysomelina beetles (Chrysomelidae)” . -
The Following Petition Document, 04-362-01P, Contains Three Parts: 1
The following petition document, 04-362-01p, contains three parts: 1. the final revised petition for nonregulated status submitted by Syngenta Seeds, Inc. (Syngenta) on August 2, 2006, for the corn rootworm protected transformation event MIR604 in Zea mays (corn), USDA APHIS number 04-362-01p (which APHIS has deemed complete); 2. a letter of completeness sent to Syngenta by USDA APHIS Biotechnology Regulatory Services (BRS) on July 25, 2006, which identified deficiencies and items to correct in an earlier version of this same petition; and 3. the earlier version of the petition submitted by Syngenta on May 17, 2006. As both versions of the petition are required for readers to understand the questions and responses within the letter of completeness, USDA APHIS BRS has assembled this document with both versions of the petition included. Petition for the Determination of Non-Regulated Status Corn Rootworm Protected Transformation Event MIR604 Revised The undersigned submits this petition under 7 CFR 340.6 to Request that the Administrator, Animal and Plant Health Inspection Service, make a determination that the article should not be regulated under 7 CFR part 340. Submitted by: Henry-York Steiner Regulatory Affairs Manager Syngenta Seeds, Inc. 3054 East Cornwallis Road Research Triangle Park, NC 27709-2257 Phone: (919) 541-8652 Fax: (919) 541-8535 Contributing Authors: Robert Joseph1, Linda Meyer1, Alan Raybould2, John Steffens1, Jeff Stein1 and Demetra Vlachos1 1Syngenta Seeds, Inc., 3054 East Cornwallis Road, Research Triangle Park, NC -
Pests of Trees and Shrubs
Pests of Trees and Shrubs Cottonwood leaf beetle Chrysomela scripta Order Coleoptera, Family Chrysomelidae; leaf beetles Native pest Host plants: Cottonwood, other poplars and several species of willows, particularly basket willow (Salix viminalis) Description: Adult beetles are 6 mm long. They are light yellow with black stripes on their wing covers. Mature larvae are blackish with two white spots on each side. They are about 12 mm long. Life history: Adults emerge in early spring, feeding on bark and new leaves. Females lay yellow, oval eggs in Defoliation caused by cottonwood leaf beetle adults. (102) clusters under leaves. Young larvae are gregarious feeders, Photo: Whitney Cranshaw skeletonizing leaves. Older larvae feed separately, consuming entire leaves, with the exception of the larger veins. There are two to four generations a year. Overwintering: Adults under loose bark or in grass clumps. Damage symptoms: Adults remove leaf tissue and cause damage to leaves. Young larvae skeletonize leaves; older larvae consume all but large veins. Severe infestations occasionally cause defoliation. Monitoring: In May look for skeletonization of leaves or for shot hole damage. Look again in July for similar damage caused by the second generation of beetles. Adults and larvae are both visible on damaged foliage. Cultural control: Pubescent varieties tend to offer some resistance. Feeding and defoliation caused by cottonwood leaf beetle Chemical control: Early instar larvae may be controlled larvae. (101) by applications of Bacillus thuringiensis var. tenebrionis. Photo: Whitney Cranshaw Chemical sprays in May or July before larvae pupate may be effective, but look for the presence of beneficial insect predators before spraying. -
Contributions to Understand the Evolutionary and Molecular Dynamics of Chemical Defense in Leaf Beetles
Identification and characterization of defense related enzymes in Chrysomelina larvae (Coleoptera: Chrysomelidae): Contributions to understand the evolutionary and molecular dynamics of chemical defense in leaf beetles Dissertation zur Erlangung des akademischen Grades doctor rerum naturalium (Dr. rer. nat.) vorgelegt dem Rat der Biologisch-Pharmazeutischen Fakultät der Friedrich-Schiller-Universität Jena von Diplom-Biologe Roy Kirsch geboren am 18.08.1979 in Jena Gutachter: Prof. Wilhelm Boland, MPI für Chemische Ökologie, Jena Prof. David Heckel, MPI für Chemische Ökologie, Jena Prof. Monika Hilker, FU Berlin Verteidigung: 20.06.2011 LIST OF CONTENTS 1 Introduction 5 1.1 General Introduction: Herbivorous insect – host plant interaction 5 1.2 Different molecular levels of host plant adaptations in leaf beetles (Chrysomelidae) of the subfamily Chrysomelinae 6 1.2.1 Defense in Chrysomelinae with special emphasis on subtribe Chrysomelina glandular chemical defense 7 1.2.2 Host plant influence and origin of Chrysomelina defensive compounds 9 1.2.3 Transport mechanisms of defensive compound precursors into the Chrysomelina larval glandular reservoir 11 1.2.4 Biosynthesis of defensive compounds by final enzymatic steps in the glandular reservoir 12 1.3 An introduction to the investigated species 14 1.3.1 Biology of Chrysomela lapponica 14 1.3.2 Biology of Phratora vitellinae 16 1.4 Aims and scope of the thesis 17 2 Overview of manuscripts 21 3 Manuscripts 24 Manuscript 1 24 Manuscript 2 37 Manuscript 3 51 4 General Discussion 62 4.1 Evolution