Biological Pest Control
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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. -
Effects of Host Plants, Temperature Regimes, and Mating Scenarios on the Population Dynamics of the Cabbage Whitefly Aleyrodes Proletella L
Effects of host plants, temperature regimes, and mating scenarios on the population dynamics of the cabbage whitefly Aleyrodes proletella L. (Hemiptera: Aleyrodidae) Dissertation zur Erlangung des Doktorgrades der Fakultät für Agrarwissenschaften der Georg-August-Universität Göttingen vorgelegt von Khaldon Askoul geboren in Swaida (Syrien) Göttingen, April 2017 _______________________________________________________ ____________ D 7 1. Referentin/Referent: Prof. Dr. Stefan Vidal 2. Korreferentin/Korreferent: Dr. Rainer Meyhöfer Tag der mündlichen Prüfung: 20.06.2017 Für meine Familie Table of contents Table of contents Summary ................................................................................................................................. 1 General introduction .............................................................................................................. 4 Objective ................................................................................................................................. 9 Chapter 1 .............................................................................................................................. 10 Life history parameters of Aleyrodes proletella L. (Hemiptera: Aleyrodidae) on different host plants ............................................................................................................................ 10 Chapter 2 .............................................................................................................................. 11 Effects -
Biopesticides: State of the Art and Future Opportunities James N
Entomology Publications Entomology 11-2014 Biopesticides: State of the Art and Future Opportunities James N. Seiber University of California - Davis Joel R. Coats Iowa State University, [email protected] Stephen O. Duke United States Department of Agriculture Aaron D. Gross Iowa State University Follow this and additional works at: http://lib.dr.iastate.edu/ent_pubs Part of the Entomology Commons The ompc lete bibliographic information for this item can be found at http://lib.dr.iastate.edu/ ent_pubs/300. For information on how to cite this item, please visit http://lib.dr.iastate.edu/ howtocite.html. This Article is brought to you for free and open access by the Entomology at Iowa State University Digital Repository. It has been accepted for inclusion in Entomology Publications by an authorized administrator of Iowa State University Digital Repository. For more information, please contact [email protected]. Biopesticides: State of the Art and Future Opportunities Abstract The use of biopesticides and related alternative management products is increasing. New tools, including semiochemicals and plant-incorporated protectants (PIPs), as well as botanical and microbially derived chemicals, are playing an increasing role in pest management, along with plant and animal genetics, biological control, cultural methods, and newer synthetics. The og al of this Perspective is to highlight promising new biopesticide research and development (R&D), based upon recently published work and that presented in the American Chemical Society (ACS) symposium “Biopesticides: State of the Art and Future Opportunities,” as well as the authors’ own perspectives. Although the focus is on biopesticides, included in this Perspective is progress with products exhibiting similar characteristics, namely those naturally occurring or derived from natural products. -
Insects Parasitoids: Natural Enemies of Helicoverpa
Queensland the Smart State insects Parasitoids: Natural enemies of helicoverpa Introduction Helicoverpa caterpillars (often called heliothis) are serious pests of many crops in Australia. A range of parasitoid and predatory insects attack helicoverpa. Identifying and conserving these beneficial insects is fundamental to implementing pest management with a reduced reliance on chemical insecticides. This brochure describes the most important parasitoids of helicoverpa in Australian broadacre crops. Parasitoids versus parasites: What’s the difference? Parasitoids kill their hosts; parasites (such Figure 1. Netelia producta is one of the as lice and fleas) do not. All the insects most commonly encountered parasitoids in this brochure are parasitoids. Despite of helicoverpa. Females lay their eggs onto this difference, the terms parasitoid and caterpillars, and the hatching wasp larva parasite are often used interchangeably, if feeds on its host, eventually killing it. inaccurately. Parasitoids such as Netelia can be important biological control agents of helicoverpa in crops. (Photo: K. Power) All comments about parasitoid abundance in this publication are based on field observations in southern Queensland farming systems. These patterns may not occur in all parts of Australia. About parasitoids What is a parasitoid? How do parasitoids find their A parasitoid is an insect that kills (parasitises) hosts? its host — usually another insect — in Many adult parasitoids find their host by order to complete its lifecycle. In Australia, smell. They can detect the direct odour of helicoverpa are parasitised by many species the host itself, or odours associated with host of wasps and flies. All helicoverpa immature activity, such as plant damage or caterpillar stages are parasitised (that is, egg, caterpillar frass (dung). -
Seven Biopesticide Active Ingredients You Should Know About
Certis USA for CAPCA Adviser Seven Biopesticide Active Ingredients You Should Know About By Tim Damico, Executive VP-NAFTA, Certis USA Biological pesticides are often referred to as soft materials. It is Isaria fumosorosea. This fungus is highly pathogenic toward a broad true that their impact is soft to the environment, beneficial insects, range of pests, including whiteflies, aphids, thrips, soil-dwelling wildlife, spray applicators and farm crews. insects and spider mites. Spores applied as a foliar spray or soil drench germinate on contact with the target pest, and the growing But there is nothing soft about how biopesticides kill pests. fungus then penetrates through the cuticle or natural openings to proliferate inside. The insect or mite stops feeding and dies soon These seven common biopesticide active ingredients are formulated afterward, often with dark spots at infection points as the only from naturally occurring bacteria, fungi and viruses. Like the visible sign of fungal infection. I. fumosorosea can infect all life pathogenic diseases and insect pests they control, these beneficial stages of the pest (eggs, nymphs, pupae and adults). organisms must employ survival strategies to live. These strategies or modes of action allow them to biologically decimate their target Bacillus amyloliquefaciens. B. amyloliquefaciens is a broad spectrum pest species. preventive fungicide/bacteriacide for foliar and soil application. This bacterium rapidly colonizes root hairs, leaves and other plant Yet as destructive as they are to their target pests, beneficial bacteria, fungi and viruses cannot infect or harm non-target species. Their modes of action are specific to certain pests. A virus Paecilomyces lilacinus fungus engulfing nematode eggs. -
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.). -
Darkling Beetles and Mealworms Theresa A
Darkling Beetles and Mealworms Theresa A. Dellinger and Eric R. Day, Department of Entomology, Virginia Tech Description Darkling beetles belong in the beetle family Tenebrionidae, which consists of more than 20,000 species of beetles. Adult darkling beetles widely range in shape and size, with most measuring from 2 – 19 mm (0.13” – 0.75”). Adults are usually a reddish-brown to brownish-black in color and can be shiny or dull. The elytra (the wing covers) can be smooth, grooved, or otherwise sculptured. Most do not have colorful patterns on their wing covers. Adults are most active at night and tend to avoid bright lights. Darkling beetle larvae are often referred to as mealworms or false wireworms. They are long, hard-bodied grubs with a cylindrical shape and are shiny yellow-brown to darKer brown in color. They are active crawlers. Yellow mealworm larva, top. Dark mealworm larva, bottom. Clemson University-USDA Cooperative Adult yellow mealworm, Tenebrio molitor. Extension Slide Series, Bugwood.org. Clemson University-USDA Cooperative Extension Slide Series, Bugwood.org. Life Cycle Darkling beetles have a complete life cycle with egg, larval, pupal, and adult stages. Most species of darkling beetles have a slow rate of development and may live for a year as an adult. Species living on grains or other stored products may develop faster. Habitat/Distribution Darkling beetles are found throughout the world except for places with very cold climates. They are scavengers and omnivores, feeding on decomposing plant material, dead insects, fungi, and stored products. Only a handful of darkling beetles are considered pests; the vast majority of them live in the wild and pose no harm. -
Integrated Pest Managemnent ~~R, Him4 T
Integrated Pest Managemnent ~~r, him4 t. I~ f4 ,..,.. 9,.. i Ulf U k gA, fi 0I,. i f. Council on Environmental Quality Integrated Pest Management December 1979 Written by Dale G. Bottrell K' Preface For many centuries human settlements, both agricultural and urban, have had to contend with a variety of unwanted and sometimes harmful insects, weeds, microorgan isms, rodents, and other organisms-collectively, "pests." During the use of chemical last four decades, p'sticides has become the predominant method of controlling these unwanted organisms in much of the world, including the United States. synthetic Production of organic pesticides in this countty alone has increased from less than 500,000 pounds in 1951 to an estimated 1.4 billion pounds in 1977. A decade ago, there was rising public concern over the accumulation pesticides of in the environment, with resulting adverse effects on some fish and wildlife populations and hazards to human health. In response to the problems, the Council on Environmental Quality undertook a study of alternative methods Integrated of pest control. Pest Management, published in 1972, stimulated increased national and international interest in integrated pest management-IPM-as an cient, economically effi environmentally preferable approach to pest control, particularly in agriculture. Since then much has been learned about the effects of pesticides, and programs have been developed which put the concept of IPM into practice. began a In 1976 the Council more comprehensive review of integrated pest management in the United States, giving attention to the potential for IPM programs in forestry, public health, urban systems and as well as in agriculture. -
Breeding Strategies in Females of the Parasitoid Wasp Spalangia Endius: Effects of Mating Status and Size
P1: VENDOR/GXB Journal of Insect Behavior [joib] pp476-joir-371890 May 1, 2002 16:4 Style file version Feb 08, 2000 Journal of Insect Behavior, Vol. 15, No. 2, March 2002 (C 2002) Breeding Strategies in Females of the Parasitoid Wasp Spalangia endius: Effects of Mating Status and Size B. H. King1 Accepted October 29, 2001; revised November 28, 2001 Does the mating status or body size of a female parasitoid wasp affect her host size choice or propensity to burrow? In Spalangia endius, using smaller hosts appears to reduce a female’s cost of parasitization but not her son’s fit- ness. However, virgin females, which produce only sons, did not preferentially parasitize smaller hosts. Mated females also showed no host size preference. Mated females burrowed more than virgins in the presence of hosts, although not in their absence. Burrowing may reduce a mated female’s harassment from males, and not burrowing may increase a virgin female’s chance of mating because males avoid burrowing. Mating did not increase female longevity. Greater female size increased the offspring production of mated females bur- rowing for hosts but not in the absence of burrowing and not in virgin females. A female’s size had no significant effect on whether her first drill attempt was on a large or a small host or on the duration of her successful drills. KEY WORDS: breeding strategies; arrhenotoky; virgin; host size; body size; parasitoid. INTRODUCTION The evolution of behaviors is often described in terms of costs and benefits. Individuals are expected to behave in ways which maximize net benefits. -
Y Su Parasitoide Encarsia Inaron (Hymenoptera: Aphelinidae) En Morelos, México
ISSN 0065-1737 Acta Zoológica MexicanaActa Zool. (n.s.), Mex. 27(3): (n.s.) 879-882 27(3) (2011) Nota Científica (Short Communication) PRIMER REGISTRO DE SIPHONINUS PHILLYREAE (HEMIPTERA: ALEYRODIDAE) Y SU PARASITOIDE ENCARSIA INARON (HYMENOPTERA: APHELINIDAE) EN MORELOS, MÉXICO Myartseva, S. N. & C. Lázaro-Castellanos. 2011. First record of Siphoninus phillyreae (Hemiptera: Aleyrodidae) and its parasitoid Encarsia inaron (Hymenoptera: Aphelinidae) in Morelos, Mexico. Acta Zoológica Mexicana (n. s.), 27(3): 879-882. ABSTRACT. This is the first record of the ash whitefly Siphoninus phillyreae (Haliday, 1835) and its parasitoid Encarsia inaron (Walker, 1839) on Fraxinus sp. in Morelos, Mexico. Las moscas blancas (Hemiptera: Aleyrodidae) son insectos fitófagos de gran impor- tancia que atacan una amplia diversidad de cultivos, plantas ornamentales y árboles de sombra como el fresno (Fraxinus sp.), el cual es plantado por gobiernos locales en las calles de las ciudades formando parte del paisaje urbano. Las moscas blancas se han estudiado durante muchos años por su importancia económica y biológica, se ali- mentan en las hojas y ovipositan en el tejido foliar donde existen otros competidores, además de ser un área frecuentada por enemigos naturales (Gerling 2002). Los afelí- nidos (Hymenoptera) son efectivos agentes de control biológico de moscas blancas e insectos escama (Williams 1996), donde muchas de las especies del género Encarsia son parasitoides primarios de Aleyrodidae y Diaspididae (Hemiptera) (Polaszek et al. 1999, Manzari et al. 2002). El 1º marzo de 2010, se colectaron hojas de fresno con adultos y pupas de mosca blanca en la ciudad de Cuernavaca, Morelos, las cuales fueron trasladadas al labora- torio del primer autor en la Facultad de Agronomía de la Universidad Autónoma de Tamaulipas, y colocadas en cajas Petri para esperar la emergencia de parasitoides. -
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 -
Biological Pest Control
■ ,VVXHG LQ IXUWKHUDQFH RI WKH &RRSHUDWLYH ([WHQVLRQ :RUN$FWV RI 0D\ DQG -XQH LQ FRRSHUDWLRQ ZLWK WKH 8QLWHG 6WDWHV 'HSDUWPHQWRI$JULFXOWXUH 'LUHFWRU&RRSHUDWLYH([WHQVLRQ8QLYHUVLW\RI0LVVRXUL&ROXPELD02 ■DQHTXDORSSRUWXQLW\$'$LQVWLWXWLRQ■■H[WHQVLRQPLVVRXULHGX AGRICULTURE Biological Pest Control ntegrated pest management (IPM) involves the use of a combination of strategies to reduce pest populations Steps for conserving beneficial insects Isafely and economically. This guide describes various • Recognize beneficial insects. agents of biological pest control. These strategies include judicious use of pesticides and cultural practices, such as • Minimize insecticide applications. crop rotation, tillage, timing of planting or harvesting, • Use selective (microbial) insecticides, or treat selectively. planting trap crops, sanitation, and use of natural enemies. • Maintain ground covers and crop residues. • Provide pollen and nectar sources or artificial foods. Natural vs. biological control Natural pest control results from living and nonliving Predators and parasites factors and has no human involvement. For example, weather and wind are nonliving factors that can contribute Predator insects actively hunt and feed on other insects, to natural control of an insect pest. Living factors could often preying on numerous species. Parasitic insects lay include a fungus or pathogen that naturally controls a pest. their eggs on or in the body of certain other insects, and Biological pest control does involve human action and the young feed on and often destroy their hosts. Not all is often achieved through the use of beneficial insects that predacious or parasitic insects are beneficial; some kill the are natural enemies of the pest. Biological control is not the natural enemies of pests instead of the pests themselves, so natural control of pests by their natural enemies; host plant be sure to properly identify an insect as beneficial before resistance; or the judicious use of pesticides.