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Research Article Ecological Observations of Native Geocoris Pallens and G
Hindawi Publishing Corporation Psyche Volume 2013, Article ID 465108, 11 pages http://dx.doi.org/10.1155/2013/465108 Research Article Ecological Observations of Native Geocoris pallens and G. punctipes Populations in the Great Basin Desert of Southwestern Utah Meredith C. Schuman, Danny Kessler, and Ian T. Baldwin Department of Molecular Ecology, Max Planck Institute for Chemical Ecology, Hans-Knoll-Straße¨ 8, 07745 Jena, Germany Correspondence should be addressed to Ian T. Baldwin; [email protected] Received 5 November 2012; Accepted 16 April 2013 Academic Editor: David G. James Copyright © 2013 Meredith C. Schuman et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Big-eyed bugs (Geocoris spp. Fallen,´ Hemiptera: Lygaeidae) are ubiquitous, omnivorous insect predators whose plant feeding behavior raises the question of whether they benefit or harm plants. However, several studies have investigated both the potential of Geocoris spp. to serve as biological control agents in agriculture and their importance as agents of plant indirect defense in nature. These studies have demonstrated that Geocoris spp. effectively reduce herbivore populations and increase plant yield. Previous work has also indicated that Geocoris spp. respond to visual and olfactory cues when foraging and choosing their prey and that associative learning of prey and plant cues informs their foraging strategies. For these reasons, Geocoris spp. have become models for the study of tritrophic plant-herbivore-predator interactions. Here, we present detailed images and ecological observations of G. pallens Stal˚ and G. -
Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America North of Mexico with a Key to Species
Zootaxa 2835: 30–40 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Review of Acanthocephala (Hemiptera: Heteroptera: Coreidae) of America north of Mexico with a key to species J. E. McPHERSON1, RICHARD J. PACKAUSKAS2, ROBERT W. SITES3, STEVEN J. TAYLOR4, C. SCOTT BUNDY5, JEFFREY D. BRADSHAW6 & PAULA LEVIN MITCHELL7 1Department of Zoology, Southern Illinois University, Carbondale, Illinois 62901, USA. E-mail: [email protected] 2Department of Biological Sciences, Fort Hays State University, Hays, Kansas 67601, USA. E-mail: [email protected] 3Enns Entomology Museum, Division of Plant Sciences, University of Missouri, Columbia, Missouri 65211, USA. E-mail: [email protected] 4Illinois Natural History Survey, University of Illinois at Urbana-Champaign, Illinois 61820, USA. E-mail: [email protected] 5Department of Entomology, Plant Pathology, & Weed Science, New Mexico State University, Las Cruces, New Mexico 88003, USA. E-mail: [email protected] 6Department of Entomology, University of Nebraska-Lincoln, Panhandle Research & Extension Center, Scottsbluff, Nebraska 69361, USA. E-mail: [email protected] 7Department of Biology, Winthrop University, Rock Hill, South Carolina 29733, USA. E-mail: [email protected] Abstract A review of Acanthocephala of America north of Mexico is presented with an updated key to species. A. confraterna is considered a junior synonym of A. terminalis, thus reducing the number of known species in this region from five to four. New state and country records are presented. Key words: Coreidae, Coreinae, Acanthocephalini, Acanthocephala, North America, review, synonymy, key, distribution Introduction The genus Acanthocephala Laporte currently is represented in America north of Mexico by five species: Acan- thocephala (Acanthocephala) declivis (Say), A. -
A Comparative Study of Two Seed Bugs, Geocoris
A COMPARATIVE STUDY OF TWO SEED BUGS, GEOCORIS BULLATUS (SAY) AND G. DISCOPTERUS STAL (HEMIPTERA: LYGAEIDAE) IN THE YUKON. By JENNIFER J. ROBINSON B.Sc. Trent University, 1980 A THESIS SUBMITTED IN PARTIAL FULFILLMENT OF THE REQUIREMENTS FOR THE DEGREE OF MASTER OF SCIENCE in THE FACULTY OF GRADUATE STUDIES DEPARTMENT OF ZOOLOGY We accept this thesis as conforming te trie required standard June, 1985 (c) Jennifer J. Robinson, 1985 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of The University of British Columbia 1956 Main Mall Vancouver, Canada V6T 1Y3 )E-6 C3/81) Abstract Geocoris bullatus (Say 1831), (Henriptera: Lygaeidae) has been collected and studied across North America but the present work is the o first detailed study of western North American CL discopterus Stal 1874. In fact, it has been claimed that 6^. discopterus is solely a species of the east. As the two species are taxonomically difficult to separate, when they were apparently discovered together at several localities in the southwestern Yukon, a detailed investigation of their systematics and distribution seemed necessary. Species status of Yukon Q. bullatus and iG. -
Biological Control of Insect Pests in the Tropics - M
TROPICAL BIOLOGY AND CONSERVATION MANAGEMENT – Vol. III - Biological Control of Insect Pests In The Tropics - M. V. Sampaio, V. H. P. Bueno, L. C. P. Silveira and A. M. Auad BIOLOGICAL CONTROL OF INSECT PESTS IN THE TROPICS M. V. Sampaio Instituto de Ciências Agrária, Universidade Federal de Uberlândia, Brazil V. H. P. Bueno and L. C. P. Silveira Departamento de Entomologia, Universidade Federal de Lavras, Brazil A. M. Auad Embrapa Gado de Leite, Empresa Brasileira de Pesquisa Agropecuária, Brazil Keywords: Augmentative biological control, bacteria, classical biological control, conservation of natural enemies, fungi, insect, mite, natural enemy, nematode, predator, parasitoid, pathogen, virus. Contents 1. Introduction 2. Natural enemies of insects and mites 2.1. Entomophagous 2.1.1. Predators 2.1.2. Parasitoids 2.2. Entomopathogens 2.2.1. Fungi 2.2.2. Bacteria 2.2.3. Viruses 2.2.4. Nematodes 3. Categories of biological control 3.1. Natural Biological Control 3.2. Applied Biological Control 3.2.1. Classical Biological Control 3.2.2. Augmentative Biological Control 3.2.3. Conservation of Natural Enemies 4. Conclusions Glossary UNESCO – EOLSS Bibliography Biographical Sketches Summary SAMPLE CHAPTERS Biological control is a pest control method with low environmental impact and small contamination risk for humans, domestic animals and the environment. Several success cases of biological control can be found in the tropics around the world. The classical biological control has been applied with greater emphasis in Australia and Latin America, with many success cases of exotic natural enemies’ introduction for the control of exotic pests. Augmentative biocontrol is used in extensive areas in Latin America, especially in the cultures of sugar cane, coffee, and soybeans. -
THE USE of a WINGLESS TWO SPOT LADYBIRD Adalia Bipunctata (Coleoptera: Coccinellidae) AS a BIOLOGICAL CONTROL AGENT of APHIDS
THE USE OF A WINGLESS TWO SPOT LADYBIRD Adalia bipunctata (Coleoptera: Coccinellidae) AS A BIOLOGICAL CONTROL AGENT OF APHIDS Ana Rita Chico Registration nr 770531 004 100 MSc. Organic Agriculture ENT 80439- Thesis Entomology Supervisor: Peter de Jong Examiner: Marcel Dicke Chairgroup Entomology Wageningen University Wageningen UR “If we knew what we were doing, it would not be called research, would it?” Albert Einstein 2 THE USE OF A WINGLESS TWO SPOT LADYBIRD Adalia bipunctata (Coleoptera: Coccinellidae) AS A BIOLOGICAL CONTROL AGENT OF APHIDS A.R. Chico November 2005 Chairgroup Entomology Wageningen University Binnenhaven 7 6709 PD, Wageningen 3 TABLE OF CONTENTS PREFACE.............................................................................................................................................................. 5 1. INTRODUCTION............................................................................................................................................. 6 1.1. BIOLOGICAL CONTROL OF APHIDS WITH PREDATORY LADYBIRDS ................................................................ 6 1.1.1. Ladybirds- an introduction.................................................................................................................. 6 1.1.2. Ladybirds as biological control agents of aphids................................................................................ 7 1.2. BACKGROUND STORY ON THE WINGLESS LADYBIRD .................................................................................... 8 1.3. SCIENTIFIC -
Predation of Adalia Tetraspilota (Hope) (Coleoptera: Coccinellidae) on Green Peach Aphid (Myzus Persicae
& Herpeto gy lo lo gy o : h C it u n r r r e O n Joshi et al., Entomol Ornithol Herpetol 2012, 1:1 , t y R g e o l s DOI:10.4172/2161-0983.1000101 o e a m r o c t h Entomology, Ornithology & Herpetology n E ISSN: 2161-0983 ResearchResearch Article Article OpenOpen Access Access Predation of Adalia tetraspilota (Hope) (Coleoptera: Coccinellidae) on Green Peach Aphid (Myzus persicae. Sulzer) Joshi PC2*, Khamashon L2 and Kaushal BR1 1Department of Zoology, D.S.B. Campus Kumaun University, Nainital, Uttarakhand, India 2Department of Zoology and Environmental Sciences, Gurukula Kangri University, Haridwar, India Abstract Studies on prey consumption of larvae and adults of Adalia tetraspilota (Hope) (Coleoptera: Coccinellidae) was conducted in the laboratory on green peach aphid, Myzus persicae (Sulzer) (Homoptera: Aphididae). In larval form 4th instar was the most efficient consumer with an average of 39.96 ± 1.04 aphids larva-1day-1 followed by 3rd instar with an average of 20.90 ± 0.58 larva-1day-1. Feeding potentials of adult coccinellids increased with increase in age. In female the highest consumption of aphids was recorded on the 23rd day of its emergence while in case of male it was recorded on 24th day. Female adult consumed more aphids (39.83 ± 11.39 aphids day-1) than male (31.70 ± 8.07 aphids day-1). Keywords: Coccinellidae; Adalia tetraspilota; Myzus persicae; Larva; Instar Age Number of aphids consumed Adult male; Adult female; Feeding (days) V1 V2 V3 V4 Mean ± SD First 1 2 3 3 2 2.50 ± 0.58 Introduction 2 4 4 5 5 4.50 ± 0.57 Mean 3 ± 1.41 3.5 ± 0.71 4 ± 1.41 3.5 ± 2.21 3.50 ± 0.41 Biological control is a component of integrated pest management Second 3 8 8 7 7 7.50 ± 0.57 strategy which consists of mostly the natural enemies of insect pests 4 10 11 11 12 11.00 ± 0.82 5 11 12 14 14 12.75 ± 1.5 i.e, predators, parasitoids and pathogen. -
Arthropod Pest Management in Greenhouses and Interiorscapes E
Arthropod Pest Management in Greenhouses and Interiorscapes E-1011E-1011 OklahomaOklahoma CooperativeCooperative ExtensionExtension ServiceService DivisionDivision ofof AgriculturalAgricultural SciencesSciences andand NaturalNatural ResourcesResources OklahomaOklahoma StateState UniversityUniversity Arthropod Pest Management in Greenhouses and Interiorscapes E-1011 Eric J. Rebek Extension Entomologist/ Ornamentals and Turfgrass Specialist Michael A. Schnelle Extension Ornamentals/ Floriculture Specialist ArthropodArthropod PestPest ManagementManagement inin GreenhousesGreenhouses andand InteriorscapesInteriorscapes Insects and their relatives cause major plant ing a hand lens. damage in commercial greenhouses and interi- Aphids feed on buds, leaves, stems, and roots orscapes. Identification of key pests and an un- by inserting their long, straw-like, piercing-suck- derstanding of appropriate control measures are ing mouthparts (stylets) and withdrawing plant essential to guard against costly crop losses. With sap. Expanding leaves from damaged buds may be tightening regulations on conventional insecti- curled or twisted and attacked leaves often display cides and increasing consumer sensitivity to their chlorotic (yellow-white) speckles where cell con- use in public spaces, growers must seek effective tents have been removed. A secondary problem pest management alternatives to conventional arises from sugary honeydew excreted by aphids. chemical control. Management strategies cen- Leaves may appear shiny and become sticky from tered around -
(LINNAEUS, 1758) in the SOUTH of WESTERN SIBERIA, RUSSIA (CHILOPODA: SCUTIGEROMORPHA: SCUTIGERIDAE) 1Altai State University, Lenina Avenue, 61, Barnaul 656049, Russia
428 Бiологiчний вiсник UDC 595.624 Nefediev P.S.1, Tuf I.H.2, Dyachkov Yu.V.1, Efimov D.A.3 FIRST RECORD OF SCUTIGERA COLEOPTRATA (LINNAEUS, 1758) IN THE SOUTH OF WESTERN SIBERIA, RUSSIA (CHILOPODA: SCUTIGEROMORPHA: SCUTIGERIDAE) 1Altai State University, Lenina Avenue, 61, Barnaul 656049, Russia. E-mail: [email protected] 2Palacký University, Šlechtitelů 27, Olomouc 77900, Czech Republic. E-mail: [email protected] 3Kemerovo State University, Krasnaya Street, 6, Kemerovo 650043, Russia. E-mail: [email protected] The order, family, genus and species of the house centipede are new to Asian Russia’s list: Scutigeromorpha, Scutigeridae, Scutigera Lamark, 1801, and Scutigera coleoptrata (Linnaeus, 1758). All records of the species in the south of western Siberia appear to be associated with synanthropic habitats. Distributional remarks are provided, all currently reported findings being mapped as well. Key words: house centipede, Scutigera coleoptrata, Scutigeridae, Scutigeromorpha, anthropochore, faunistics, introduction, Siberia. INTRODUCTION The centipede fauna of Siberia is very poorly-studied. All former research has been devoted to Lithobiomorpha and Geophilomorpha in natural habitats. Investigating anthropogenic habitats in the south of western Siberia, we have currently found the house centipede Scutigera coleoptrata (Linnaeus, 1758). Both the order Scutigeromorpha, and the family Scutigeridae it belongs to, are almost worldwide, distributed in all continents, on all major islands and many oceanic islands with the exception of Antarctica, and many records refer to introduced populations of Scutigera coleoptrata (Bonato & Zapparoli, 2011). The samples treated below have been deposited in the collection of the Altai State University, Barnaul, Russia (ASU). RESULTS SCUTIGEROMORPHA Pocock, 1895 SCUTIGERIDAE Gervais, 1837 Scutigera coleoptrata (Linnaeus, 1758) ISSN 2225-5486 (Print), ISSN 2226-9010 (Online). -
Exocrine Secretions of Wheel Bugs (Heteroptera: Reduviidae: Arilus Spp.): Clarifi Cation and Chemistry Jeffrey R
Exocrine Secretions of Wheel Bugs (Heteroptera: Reduviidae: Arilus spp.): Clarifi cation and Chemistry Jeffrey R. Aldricha,b,*, Kamlesh R. Chauhanc, Aijun Zhangc, and Paulo H. G. Zarbind a Affi liate Department of Entomology, University of California, Davis, CA, USA b J. R. Aldrich consulting LLC, 519 Washington Street, Santa Cruz, CA 95060, USA. E-mail: [email protected] c USDA-ARS Invasive Insect Biocontrol & Behavior Laboratory, 10300 Baltimore Avenue, Bldg. 007, rm301, BARC-West, Beltsville, MD 20705, USA d Universidade Federal do Paraná, Departamento de Química, Laboratório de Semioquímicos, CP 19081, 81531 – 980, Curitiba – PR, Brazil * Author for correspondence and reprint requests Z. Naturforsch. 68 c, 522 – 526 (2013); received August 21/November 6, 2013 Wheel bugs (Heteroptera: Reduviidae: Harpactorinae: Arilus) are general predators, the females of which have reddish-orange subrectal glands (SGs) that are eversible like the os- meteria in some caterpillars. The rancid odor of Arilus and other reduviids actually comes from Brindley's glands, which in the North (A. cristatus) and South (A. carinatus) American wheel bugs studied emit similar blends of 2-methylpropanoic, butanoic, 3-methylbutanoic, and 2-methylbutanoic acids. The Arilus SG secretions studied here are absolutely species- specifi c. The volatile SG components of A. carinatus include (E)-2-octenal, (E)-2-none- nal, (E)-2-decenal, (E,E)-2,4-nonadienal, (E)-2-undecenal, hexanoic acid, 4-oxo-nonanal, (E,E)-2,4-decadienal, (E,Z)-2,4- or (Z,E)-2,4-decadienal, and 4-oxo-(E)-2-nonenal; whereas in A. cristatus the SG secretion contains β-pinene, limonene, terpinolene, terpinen-4-ol, thy- mol methyl ether, α-terpineol, bornyl acetate, methyl eugenol, β-caryophyllene, caryophyllene oxide, and farnesol. -
On the Presence of Scutigera Coleoptrata (Linnaeus, 1758) (Chilopoda: Scutigeromorpha: Scutigeridae) in the Metropolitan Region, Chile
MASUMOTO, K., G. DELLACASA & M. KIUCHI 1990. On the Aphodius de Storia naturale, Milano, 114: 51-70. ● REITTER, E. 1895. Einige species of Japan. Entomological Review of Japan, 45: 145-156. ● neue Coleopteren aus Korea und China. Wiener entomologische MÜLLER, G. 1941. Nuovi Coleotteri dell’Africa Orientale. Atti del Zeitung, 14: 208-210. ● SCHMIDT, A. 1907. Zusammentellung der Museo civico di Storia naturale di Trieste, 14: 319-352. ● NEAVE, bis 1906 beschriebenen Aphodiinen. Deutsche entomologische S.A. 1939. Nomenclator Zoologicus. A List of the Names of Genera Zeitschrift, Beilage, 1907-1908: 1-141. ● SCHMIDT, A. 1910a. Col- and Subgenera in Zoology from the Tenth Edition of Linnaeus 1758 eoptera Lamellicornia, Fam. Aphodiidae. 110me Fascicule. In: P. to the End of 1935. Vol. 1, A-C. The Zoological Society of London, Wytsman (ed.), Genera Insectorum. Tervueren, 155 pp, 3 pls. ● London, xiv + 957 pp. ● PAULIAN, R. 1942. Exploration du Parc SCHMIDT, A. 1910b. Aphodiinae. Pars 20, Vol. 19(4). In: S. Schenk- National Albert. Mission G. F. de Witte (1933-35). Fasc. 35. Aphodi- ling (ed.), Coleopterorum Catalogus. W. Junk, Berlin, 111 pp. ● inae (Coleoptera Lamellicornia) Fam. Scarabaeidae. Institut des SCHMIDT, A. 1913. Erster Versuch einer Einteilung der exotischen Parcs Nationaux du Congo Belge, 143 pp., 23 pls. ● PETROVITZ, R. Aphodien in Subgenera und als Anhang einige Neubeschreibungen. 1958. Neue afrikanischen Aphodiusarten (Col. Scarab.). Entomolo- Archiv für Naturgeschichte. Abtheilung A, Original-Arbeiten, 79: 117- gische Arbeiten aus dem Museum G. Frey, 9: 140-159. ● 178. ● SCHMIDT, A. 1922. Coleoptera, Aphodiinae. In: C. Apstein PETROVITZ, R. 1962. Neue und verkannte Aphodiinae aus allen (ed.), Das Tierreich. -
House Centipedes: Lots of Legs, but Not a Hundred House Centipedes Are Predatory Arthropods That Can Be Found Both Indoors and Outdoors
http://hdl.handle.net/1813/43838 2015 Community House Centipedes: Lots of Legs, but not a Hundred House centipedes are predatory arthropods that can be found both indoors and outdoors. They prefer damp places, including basements, bathrooms and even pots of over-watered plants, where they feed on insects and spiders. As predators of other arthropods, they can be considered a beneficial organism, but are most often considered a nuisance pest when present in the home. Did you know … ? • By the Numbers: There are approximately 8,000 species of Common House Centipede (Scutigera coleoptrata Linnaeus). Photo: G. Alpert. centipedes. • Form-ally Speaking: Centipedes come in a variety of forms and sizes. Depending on the species they can be red, brown, black, white, orange, or yellow. Some species are shorter than an inch, while tropical species can be up to a foot in length! • Preying on the Predators: Larger centipedes can feed on mice, toads, and even birds. • Preference or Requirement? Centipedes prefer moist areas because they lack a waxy exoskeleton. In dry areas, centipedes can die from desiccation or drying out. Identification Common House Centipede close-up. Photo: G. Alpert. Adult house centipedes measure one to two inches in length, but may appear larger because of their 15 pair of long legs. House centipedes are yellow-gray in color, with three black stripes that span the length of the body, and black bands on their legs. The last pair of legs is very long and is modified to hold onto prey items. These and other legs can be detached defensively if grasped by a predator. -
Investigating the Use of Buckwheat Strips for the Management of Colorado Potato Beetles in Potato Production and As an Attractan
Investigating the Use of Buckwheat Strips for the Management of Colorado Potato Beetles in Potato Production and as an Attractant of Native Pollinators for Vine Crops 1. Project Summary This project consisted of two parts. The first was to see if buckwheat strips would attract beneficial predatory insects over to adjacent planted potato rows. My hypothesis was that Colorado potato beetle larvae would have reduced numbers due to the predation by beneficial insect predators attracted by the nearby buckwheat. Compared to the control plot where no buckwheat was planted, the treatment plots showed a significant increase in larvae reduction and predation by four species of predators. The second part of the project was to see if strips of buckwheat planted next to rows of cucumbers would attract native pollinators over to the vine crops to help improve pollination (and increase marketable fruit). Compared to the control plot where no buckwheat was planted, the treatment plots had greater numbers of native bees and wasps. There also was a significant difference between the number of marketable cucumbers and those that were misshapen due to poor pollination. 2. Introduction to Topic Cover crops have great benefits for vegetable production. The cover crops can suppress weeds, reduce erosion, act as a green manure providing nutrients, and adds organic matter back to the soil. Still with all of these fine properties, cover crops still are not as commonplace on an organic farm as they should be. Many small growers have land restrictions so that every piece is needed for production. Having some tied up in cover crops means reduced sales potential in the short run.