Natural and Biological Controls of Shade Tree Insect Pests

Total Page:16

File Type:pdf, Size:1020Kb

Natural and Biological Controls of Shade Tree Insect Pests Natural and Biological Controls of Shade Tree Insect Pests Whitney Cranshaw Colorado State University Natural Controls Natural Enemies Abiotic (Weather) Controls Topographic Limitations Temperature Extremes Heavy Rainfall Abiotic (Weather-related) Controls of Insects N Natural Enemies • Predators • Parasitoids • Pathogens Characteristics of Insect Predators • Immature stages actively hunt prey • Several prey are consumed in the course of development • Adults may or may not have similar food needs as immature form Some Common Arthropod Predators • Lady beetles • Assassin bugs • Ground beetles • Predatory stink • Clerid beetles bugs • Lacewings • Minute pirate bugs • Flower flies • Predatory thrips • Robber flies • Predatory mites • Mantids • All spiders Most lady beetle adults are brightly colored Photograph courtesy Jim Kalisch The “bad apple” of the lady beetle clan Eggs Adult Mexican bean beetle - a plant feeding lady beetle Larva Pupa Adults Eggs Lady Beetle Life Stages Larva Pupae Twospotted lady beetle with newly laid egg mass Lady beetles with egg masses Lady beetles lay masses of eggs near sources of food for their young Lady beetle larvae at egg hatch Lady beetle larvae Predators of small soft- bodied arthropods (aphids etc…) Some odd looking lady beetle larvae ”Woolly” looking larvae that feed on scale insects Spider mite specialists are tiny Lady beetle prepupae Lady beetle pupae Convergent lady beetles Multicolored Asian lady beetle Adult lady beetles emerging from the pupa Purchasing lady beetles? Convergent lady beetle – the lady beetle of commerce Purchasing lady beetles? Lady beetle releases are fun Clerid Beetles Coleoptera: Cleridae Clerid Beetles Adults feed on insects present on the bark Larvae feed on insects under the bark Green Lacewings Neuroptera: Chrysopidae Adult green lacewings sustain themselves on nectar and pollen Green lacewing eggs are uniquely stalked Green lacewing eggs often are laid in groups. Egg hatch has occurred in the lower picture. Photographs courtesy of Brian Valentine Left: Green lacewing larva eating aphid Right: Green lacewing larva eating leaf beetle larva Green lacewing pupae, within cocoons Green lacewing eggs are available from many suppliers that rear/distribute insects Brown Lacewings Neuroptera: Hemerobiidae Brown lacewing adults Brown lacewing larvae Flower (Syrphid) Flies Syrphid flies are excellent mimics of bees and wasps Honey Bees Flower (Syrphid) Flies Syrphid fly eggs are typically laid in an aphid colony Photograph courtesy Brian Valentine Flower fly larvae Syrphid “smear’ Predatory Hemiptera • Predatory stink bugs • Assassin bugs • Damsel bugs • Minute pirate bugs • Geocoris spp. seed bugs • Daereocoris spp. plant bugs Minute pirate bugs Hemiptera: Anthocoridae Feeding on a thrips Feeding on a small caterpillar Nymph feeding on an aphid Adult feeding on spider mite eggs Assassin Bugs Hemiptera: Reduviidae An Assassin Bug - Zelus luridus Egg mass and nymph Adult Nymph feeding on wasp Photograph by Jim Kalisch, University of Nebraska Largest regional Wheel Bug (Arilus cristatus) assassin bug Ambush Bugs Phymata spp. Clockwise from upper right: Ambush bug feeding on a sweat bee, fritillary butterfly, and honey bee. Predatory Stink Bugs Hemiptera: Pentatomidae Stink bugs with prey Spiders Order Araneae Some spiders use webbing to snare prey Some spiders hunt prey without the aid of silk Characteristics of Insect Parasitoids • Larvae develop in, rarely on, their hosts – One or more larvae develop in a single host • They are invariably lethal to the host – “parasitoids” • Adults often have different food needs – Nectar, honeydew – Pollen – Insect blood feeding may occur Common Insect Parasitoids • Parasitic Hymenoptera – Braconid wasps – Ichneumonid wasps – Chalcid wasps – Eulophid wasp – Trichogrammatid wasps • Parasitic Diptera – Tachinid flies Parasitic Wasps Ichneumonidae, Braconidae, Eulophidae, Trichogrammatidae, Encrytidae, Chalcidae and other families Parasitic wasps sustain themselves on nectar and pollen Some parasitic wasps Females possess an ovipositor (“stinger’) Photograph courtesy Brian Valentine Parasitic Wasps – Male (left) and Female (right) Ectoparasitic wasp larvae on fall webworm caterpillar host Parasitoid larvae emerging from caterpillar host Parasitoid larvae (Cotesia glomeratus) emerging from cabbageworm host and spinning pupal cocoons Cocoons of cabbageworm parasitoid Some parasitoids pupate on the insect host. Left: Buck moth caterpillar Below: Tobacco hornworm Giant Ichneumon Wasp, Parasitoid of the Pigeon Tremex Horntail Pigeon Tremex and Giant Ichneumon Wasp Fact Sheet 5.604 Pigeon tremex – a wood boring wasp of deciduous trees in decline Giant ichneumon wasp – the most spectacular natural enemy of the pigeon tremex Ovipositor Sheaths Egg parasitoids Trichogramma wasps, a type of egg parasitoid What’s wrong with this picture? Aphid parasitoids Host evaluation Oviposition Photographs courtesy of Brian Valentine Aphid Mummies Aphid showing early symptoms of parasitism Parasitized psyllids (above) and Parasitized aphids (above) and European soft scale (below) oystershell scale (below) Tachinid Flies Tachinid fly eggs on tent caterpillar (above), squash bug nymphs (upper right), Japanese beetle .
Recommended publications
  • Alien Dominance of the Parasitoid Wasp Community Along an Elevation Gradient on Hawai’I Island
    University of Nebraska - Lincoln DigitalCommons@University of Nebraska - Lincoln USGS Staff -- Published Research US Geological Survey 2008 Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island Robert W. Peck U.S. Geological Survey, [email protected] Paul C. Banko U.S. Geological Survey Marla Schwarzfeld U.S. Geological Survey Melody Euaparadorn U.S. Geological Survey Kevin W. Brinck U.S. Geological Survey Follow this and additional works at: https://digitalcommons.unl.edu/usgsstaffpub Peck, Robert W.; Banko, Paul C.; Schwarzfeld, Marla; Euaparadorn, Melody; and Brinck, Kevin W., "Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island" (2008). USGS Staff -- Published Research. 652. https://digitalcommons.unl.edu/usgsstaffpub/652 This Article is brought to you for free and open access by the US Geological Survey at DigitalCommons@University of Nebraska - Lincoln. It has been accepted for inclusion in USGS Staff -- Published Research by an authorized administrator of DigitalCommons@University of Nebraska - Lincoln. Biol Invasions (2008) 10:1441–1455 DOI 10.1007/s10530-008-9218-1 ORIGINAL PAPER Alien dominance of the parasitoid wasp community along an elevation gradient on Hawai’i Island Robert W. Peck Æ Paul C. Banko Æ Marla Schwarzfeld Æ Melody Euaparadorn Æ Kevin W. Brinck Received: 7 December 2007 / Accepted: 21 January 2008 / Published online: 6 February 2008 Ó Springer Science+Business Media B.V. 2008 Abstract Through intentional and accidental increased with increasing elevation, with all three introduction, more than 100 species of alien Ichneu- elevations differing significantly from each other. monidae and Braconidae (Hymenoptera) have Nine species purposely introduced to control pest become established in the Hawaiian Islands.
    [Show full text]
  • Wood-Destroying Insect Diagnostic Inspection
    Wood-Destroying Insect Diagnostic Inspection Category 12 Study Guide for Commercial Applicator August 2020 - ODA - Pesticide and Fertilizer Regulation- Certification and Training Section Acknowledgements The Ohio Department of Agriculture would like to thank the following entities that helped develop this study manual. Their time, effort, and expertise are greatly appreciated. Authors Susan Jones The Ohio State University Extension – Entomology Joanne Kick-Raack The Ohio State University Extension – PAT William Pound Ohio Department of Agriculture Members of the Ohio Pest Control Assoc. Editors Kelly Boubary – ODA Stephanie Boyd – ODA 3 OHIO WOOD DESTROYING INSECT INSPECTION PROGRAM TABLE OF CONTENTS Introduction 6 Chapter 1 Training and Licensing Requirements for WDI 7 Chapter 2 Understanding the Real Estate Transaction 10 Chapter 3 Reportable Wood-Destroying Insects of Ohio 13 Chapter 4 Miscellaneous Insects and Fungi Associated with Wood in Structures 33 Chapter 5 Understanding Basic Construction Technology 38 Chapter 6 Inspecting Structures 51 Chapter 7 Management Options for Wood-Destroying Insects 58 Chapter 8 Ohio Guidelines for Completing the NPMA-33 Form 70 Chapter 9 Guidelines for Soil Termiticide Treatments 75 Appendix Glossary of Terms 83 Appendix A Chapter 921 of the Ohio Revised Code (ORC) 84 Ohio Wood-Destroying Insect Inspection Program Introduction The Ohio Department of Agriculture receives numerous inquiries and complaints each year from Ohio consumers and other interested parties with concerns about Wood-Destroying Insect (WDI) inspections and reports performed during the process of real estate transactions. Based on this fact, the Ohio Department of Agriculture and the Ohio Pest Control Association have collaborated to develop and implement a mandatory training program that will establish training guidelines and provide uniform inspection procedures for all individuals performing WDI inspections and uniform guidelines for reporting the results of these inspections for real estate transactions.
    [Show full text]
  • Attraction of Trichogramma Wasps to Brassica Nigra Plants Induced by Lepidopteran Eggs
    Attraction of Trichogramma wasps to Brassica nigra plants induced by lepidopteran eggs Ilich A. Figueroa Supervisors: Nina Fatouros, Ties Huigens Examiner: Marcel Dicke MSc. Minor Thesis– ENT-80424 Report no. 010.27 MSc Plant Science Program Laboratory of Entomology Wageningen University December, 2010 Abstract Plants possess a broad spectrum of defense mechanisms against herbivore attack. The black mustard Brassica nigra, is able to display early defense mechanism against egg infestation by pierid butterflies. This plant shows induced direct defense through hypersensitive response (HR), which kills the eggs as well as indirect defense by the emission of egg-induced plant volatiles that attract egg parasitoids such as Trichogramma wasp. In this study, I investigate whether B. nigra plants infested by the small cabbage white butterfly (Pieris rapae) or the cabbage moth (Mamestra brassicae) express both kind of defense strategies, and whether plants expressing HR still attract Trichgramma wasps in the laboratory and in nature. Tests in the y-tube olfactometer showed that volatiles of plants infested with P. rapae eggs 24h after egg deposition were attractive to the egg parasitoid Trichogramma brassicae when tested against volatiles of uninfested plants. All tested P. rapae-infested plants expressed HR 24h after oviposition. In contrast, plants infested with M. brassicae eggs did not express HR. Volatiles of M. brassicae egg-infested plants were attractive to T. brassicae only when tested against clean air but not when tested against volatiles of uninfested plants. In nature, 77% of the P. rapae eggs collected from HR+ B. nigra plants died, whereby 37% because of Trichogramma parasitism. Eggs collected on HR- B.
    [Show full text]
  • A Phylogenetic Analysis of the Megadiverse Chalcidoidea (Hymenoptera)
    UC Riverside UC Riverside Previously Published Works Title A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) Permalink https://escholarship.org/uc/item/3h73n0f9 Journal Cladistics, 29(5) ISSN 07483007 Authors Heraty, John M Burks, Roger A Cruaud, Astrid et al. Publication Date 2013-10-01 DOI 10.1111/cla.12006 Peer reviewed eScholarship.org Powered by the California Digital Library University of California Cladistics Cladistics 29 (2013) 466–542 10.1111/cla.12006 A phylogenetic analysis of the megadiverse Chalcidoidea (Hymenoptera) John M. Heratya,*, Roger A. Burksa,b, Astrid Cruauda,c, Gary A. P. Gibsond, Johan Liljeblada,e, James Munroa,f, Jean-Yves Rasplusc, Gerard Delvareg, Peter Jansˇtah, Alex Gumovskyi, John Huberj, James B. Woolleyk, Lars Krogmannl, Steve Heydonm, Andrew Polaszekn, Stefan Schmidto, D. Chris Darlingp,q, Michael W. Gatesr, Jason Motterna, Elizabeth Murraya, Ana Dal Molink, Serguei Triapitsyna, Hannes Baurs, John D. Pintoa,t, Simon van Noortu,v, Jeremiah Georgea and Matthew Yoderw aDepartment of Entomology, University of California, Riverside, CA, 92521, USA; bDepartment of Evolution, Ecology and Organismal Biology, Ohio State University, Columbus, OH, 43210, USA; cINRA, UMR 1062 CBGP CS30016, F-34988, Montferrier-sur-Lez, France; dAgriculture and Agri-Food Canada, 960 Carling Avenue, Ottawa, ON, K1A 0C6, Canada; eSwedish Species Information Centre, Swedish University of Agricultural Sciences, PO Box 7007, SE-750 07, Uppsala, Sweden; fInstitute for Genome Sciences, School of Medicine, University
    [Show full text]
  • Identification Key to the Subfamilies of Ichneumonidae (Hymenoptera)
    Identification key to the subfamilies of Ichneumonidae (Hymenoptera) Gavin Broad Dept. of Entomology, The Natural History Museum, Cromwell Road, London SW7 5BD, UK Notes on the key, February 2011 This key to ichneumonid subfamilies should be regarded as a test version and feedback will be much appreciated (emails to [email protected]). Many of the illustrations are provisional and more characters need to be illustrated, which is a work in progress. Many of the scanning electron micrographs were taken by Sondra Ward for Ian Gauld’s series of volumes on the Ichneumonidae of Costa Rica. Many of the line drawings are by Mike Fitton. I am grateful to Pelle Magnusson for the photographs of Brachycyrtus ornatus and for his suggestion as to where to include this subfamily in the key. Other illustrations are my own work. Morphological terminology mostly follows Fitton et al. (1988). A comprehensively illustrated list of morphological terms employed here is in development. In lateral views, the anterior (head) end of the wasp is to the left and in dorsal or ventral images, the anterior (head) end is uppermost. There are a few exceptions (indicated in figure legends) and these will rectified soon. Identifying ichneumonids Identifying ichneumonids can be a daunting process, with about 2,400 species in Britain and Ireland. These are currently classified into 32 subfamilies (there are a few more extralimitally). Rather few of these subfamilies are reconisable on the basis of simple morphological character states, rather, they tend to be reconisable on combinations of characters that occur convergently and in different permutations across various groups of ichneumonids.
    [Show full text]
  • Unexpectedly High Levels of Parasitism of Wheat Stem Sawfly Larvae in Postcutting Diapause Chambers Author(S) :Tatyana A
    Unexpectedly High Levels of Parasitism of Wheat Stem Sawfly Larvae in Postcutting Diapause Chambers Author(s) :Tatyana A. Rand, Debra K. Waters, Thomas G. Shanower Source: The Canadian Entomologist, 143(5):455-459. 2011. Published By: Entomological Society of Canada URL: http://www.bioone.org/doi/full/10.4039/n11-023 BioOne (www.bioone.org) is a nonprofit, online aggregation of core research in the biological, ecological, and environmental sciences. BioOne provides a sustainable online platform for over 170 journals and books published by nonprofit societies, associations, museums, institutions, and presses. Your use of this PDF, the BioOne Web site, and all posted and associated content indicates your acceptance of BioOne’s Terms of Use, available at www.bioone.org/page/ terms_of_use. Usage of BioOne content is strictly limited to personal, educational, and non-commercial use. Commercial inquiries or rights and permissions requests should be directed to the individual publisher as copyright holder. BioOne sees sustainable scholarly publishing as an inherently collaborative enterprise connecting authors, nonprofit publishers, academic institutions, research libraries, and research funders in the common goal of maximizing access to critical research. 455 Unexpectedly high levels of parasitism of wheat stem sawfly larvae in postcutting diapause chambers Tatyana A. Rand, Debra K. Waters, Thomas G. Shanower Abstract*We examined rates of late-season parasitism of larvae of the wheat stem sawfly, Cephus cinctus Norton (Hymenoptera: Cephidae), by native species of Bracon F. (Hymenop- tera: Braconidae) over 8 years in Montana and North Dakota, United States of America. We found that rates of parasitism of larvae in diapause chambers reached a maximum of 46%, exceeding the previously reported maximum of 2.5% in 75% of sites and years examined.
    [Show full text]
  • Asian Giant Hornet in Washington State
    ASIAN GIANT HORNET IN WASHINGTON STATE PEST PROGRAM INTRODUCTION ASIAN Asian giant hornet (Vespa mandarinia) is the world’s largest hornet. The hornet is native to Asia, and has GIANT been recorded from Japan, Korea, Russia, China, and several other countries. In December 2019, WSDA HORNET verified the first ever sightings of Asian giant hornet in the United States. If Asian giant hornet becomes Asian giant hornet (AGH) is a predatory wasp that established, it could feeds on a wide variety of insects. The introduction have serious impacts of this species is of major concern to agriculture on the environment, because of its predation on honeybees - a few Asian economy, and giant hornets can kill an entire beehive in a matter public health of of hours. If unmanaged they could significantly Washington State. increase costs for beekeepers and potentially disrupt pollination services. They could also impact other local insect populations. While AGH does not generally attack people or pets, they can sting when threatened. If it becomes established, this hornet could have serious impacts on the environment, economy, and public health of Washington State. Some of the Asian giant hornet specimens WSDA recovered during eradication of a nest in Blaine, WA - the first ever nest found in the U.S. ASIAN GIANT HORNET | 1 identification • Usually 1.5 - 2 inches in length, with queens being substantially larger than workers or males • Large orange/yellow head with prominent eyes • Black and orange/yellow striped abdomen • Forms large colonies that usually nest in the ground, although sometimes in tree cavities lookalikes • Western cicada killers are mostly rust-orange colored and have yellow spots on the abdomen.
    [Show full text]
  • Fauna of Chalcid Wasps (Hymenoptera: Chalcidoidea, Chalcididae) in Hormozgan Province, Southern Iran
    J Insect Biodivers Syst 02(1): 155–166 First Online JOURNAL OF INSECT BIODIVERSITY AND SYSTEMATICS Research Article http://jibs.modares.ac.ir http://zoobank.org/References/AABD72DE-6C3B-41A9-9E46-56B6015E6325 Fauna of chalcid wasps (Hymenoptera: Chalcidoidea, Chalcididae) in Hormozgan province, southern Iran Tahereh Tavakoli Roodi1, Majid Fallahzadeh1* and Hossien Lotfalizadeh2 1 Department of Entomology, Jahrom branch, Islamic Azad University, Jahrom, Iran. 2 Department of Plant Protection, East-Azarbaijan Agricultural and Natural Resources Research Center, Agricultural Research, Education and Extension Organization (AREEO), Tabriz, Iran ABSTRACT. This paper provides data on distribution of 13 chalcid wasp species (Hymenoptera: Chalcidoidea: Chalcididae) belonging to 9 genera and Received: 30 June, 2016 three subfamilies Chalcidinae, Dirhininae and Haltichellinae from Hormozgan province, southern Iran. All collected species are new records for the province. Accepted: Two species Dirhinus excavatus Dalman, 1818 and Hockeria bifasciata Walker, 13 July, 2016 1834 are recorded from Iran for the first time. In the present study, D. excavatus Published: is a new species record for the Palaearctic region. An updated list of all known 13 July, 2016 species of Chalcididae from Iran is also included. Subject Editor: George Japoshvili Key words: Chalcididae, Hymenoptera, Iran, Fauna, Distribution, Malaise trap Citation: Tavakoli Roodi, T., Fallahzadeh, M. and Lotfalizadeh, H. 2016. Fauna of chalcid wasps (Hymenoptera: Chalcidoidea: Chalcididae) in Hormozgan province, southern Iran. Journal of Insect Biodiversity and Systematics, 2(1): 155–166. Introduction The Chalcididae are a moderately specious Coleoptera, Neuroptera and Strepsiptera family of parasitic wasps, with over 1469 (Bouček 1952; Narendran 1986; Delvare nominal species in about 90 genera, occur and Bouček 1992; Noyes 2016).
    [Show full text]
  • Development of Microplitiscroceipes As a Biological Sensor
    eea_743.fm Page 249 Wednesday, July 9, 2008 4:03 PM DOI: 10.1111/j.1570-7458.2008.00743.x Blackwell Publishing Ltd MINI REVIEW Development of Microplitis croceipes as a biological sensor J. K. Tomberlin1*, G. C. Rains2 & M. R. Sanford1 1Department of Entomology, Texas A&M University, College Station, TX 77845-2475, USA, and 2Department of Biological and Agricultural Engineering, University of Georgia, Tifton, GA 31783, USA Accepted: 2 May 2008 Key words: associative learning, Wasp Hound®, Hymenoptera, Braconidae, conditioning, medical diagnosis, forensics, food safety, national security, plant disease Abstract Classical conditioning, a form of associative learning, was first described in the vertebrate literature by Pavlov, but has since been documented for a wide variety of insects. Our knowledge of associative learning by insects began with Karl vonFrisch explaining communication among honeybees, Apis mellifera L. (Hymenoptera: Apidae). Since then, the honey bee has provided us with much of what we understand about associative learning in insects and how we relate the theories of learning in vertebrates to insects. Fruit flies, moths, and parasitic wasps are just a few examples of other insects that have been documented with the ability to learn. A novel direction in research on this topic attempts to harness the ability of insects to learn for the development of biological sensors. Parasitic wasps, especially Microplitis croceipes (Cresson) (Hymenoptera: Braconidae), have been conditioned to detect the odors associated with explosives, food toxins, and cadavers. Honeybees and moths have also been associatively conditioned to several volatiles of interest in forensics and national security. In some cases, handheld devices have been developed to harness the insects and observe conditioned behavioral responses to air samples in an attempt to detect target volatiles.
    [Show full text]
  • Insects That Feed on Trees and Shrubs
    INSECTS THAT FEED ON COLORADO TREES AND SHRUBS1 Whitney Cranshaw David Leatherman Boris Kondratieff Bulletin 506A TABLE OF CONTENTS DEFOLIATORS .................................................... 8 Leaf Feeding Caterpillars .............................................. 8 Cecropia Moth ................................................ 8 Polyphemus Moth ............................................. 9 Nevada Buck Moth ............................................. 9 Pandora Moth ............................................... 10 Io Moth .................................................... 10 Fall Webworm ............................................... 11 Tiger Moth ................................................. 12 American Dagger Moth ......................................... 13 Redhumped Caterpillar ......................................... 13 Achemon Sphinx ............................................. 14 Table 1. Common sphinx moths of Colorado .......................... 14 Douglas-fir Tussock Moth ....................................... 15 1. Whitney Cranshaw, Colorado State University Cooperative Extension etnomologist and associate professor, entomology; David Leatherman, entomologist, Colorado State Forest Service; Boris Kondratieff, associate professor, entomology. 8/93. ©Colorado State University Cooperative Extension. 1994. For more information, contact your county Cooperative Extension office. Issued in furtherance of Cooperative Extension work, Acts of May 8 and June 30, 1914, in cooperation with the U.S. Department of Agriculture,
    [Show full text]
  • Redalyc.Assessment of Trichogramma Species (Hymenoptera
    Acta Scientiarum. Agronomy ISSN: 1679-9275 [email protected] Universidade Estadual de Maringá Brasil Alvarenga Soares, Marcus; Demolin Leite, Germano Leão; Cola Zanuncio, José; Soares Ferreira, Cleidson; Leite Rocha, Silma; Mendes de Sá, Veríssimo Gibran Assessment of Trichogramma species (Hymenoptera: Trichogrammatidae) for biological control in cassava (Manihot esculenta Crantz) Acta Scientiarum. Agronomy, vol. 36, núm. 4, octubre-diciembre, 2014, pp. 403-408 Universidade Estadual de Maringá Maringá, Brasil Available in: http://www.redalyc.org/articulo.oa?id=303031660002 How to cite Complete issue Scientific Information System More information about this article Network of Scientific Journals from Latin America, the Caribbean, Spain and Portugal Journal's homepage in redalyc.org Non-profit academic project, developed under the open access initiative Acta Scientiarum http://www.uem.br/acta ISSN printed: 1679-9275 ISSN on-line: 1807-8621 Doi: 10.4025/actasciagron.v36i4.17744 Assessment of Trichogramma species (Hymenoptera: Trichogrammatidae) for biological control in cassava (Manihot esculenta Crantz) Marcus Alvarenga Soares1*, Germano Leão Demolin Leite2, José Cola Zanuncio3, Cleidson Soares Ferreira2, Silma Leite Rocha3 and Veríssimo Gibran Mendes de Sá4 1Programa de Pós-graduação em Produção Vegetal, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Rodovia MGT-367, Km 583, 5000, 39100-000, Diamantina, Minas Gerais, Brazil. 2Insetário George Washington Gomez de Moraes, Instituto de Ciências Agrárias, Universidade Federal de Minas Gerais, Montes Claros, Minas Gerais, Brazil. 3Departamento de Biologia Animal, Universidade Federal de Viçosa, Viçosa, Minas Gerais, Brazil. 4Faculdade de Engenharia, Universidade do Estado de Minas Gerais, João Monlevade, Minas Gerais, Brazil. *Author for correspondence. E-mail: [email protected] ABSTRACT.
    [Show full text]
  • Response of Psyttalia Humilis (Hymenoptera: Braconidae) to Olive Fruit Fly (Diptera: Tephritidae) and Conditions in California Olive Orchards
    BIOLOGICAL CONTROL-PARASITOIDS AND PREDATORS Response of Psyttalia humilis (Hymenoptera: Braconidae) to Olive Fruit Fly (Diptera: Tephritidae) and Conditions in California Olive Orchards VICTORIA Y. YOKOYAMA,1 PEDRO A. RENDO´ N,2 XIN-GENG WANG,3 SUSAN B. OPP,4 5 3 MARSHALL W. JOHNSON, AND KENT M. DAANE Environ. Entomol. 40(2): 315Ð323 (2011); DOI: 10.1603/EN10186 ABSTRACT The larval parasitoid, Psyttalia humilis (Silvestri), reared on Mediterranean fruit ßy, Ceratitis capitata (Weidemann), by USDA-APHIS-PPQ, San Miguel Petapa, Guatemala was imported into California for biological control of olive fruit ßy, Bactrocera oleae (Rossi). This study reports the results of Þeld releases and recovery of P. humilis in California, and laboratory investigations to determine the effects of food provision, high temperature, and insecticidal bait spray on the parasi- toidÕs survival and fecundity. Parasitoids (3,613Ð7,823) were released in Orland, San Juan Bautista, Cayucos, Sylmar, Santa Barbara, and San Diego during October through December 2006. Mean daily temperatures at the release sites ranged from 10.7ЊC in Orland to 20.9ЊC in San Juan Bautista. The lowest (0.5) and highest (29.7) mean number of adult B. oleae per day per trap was captured in Orland and Sylmar, while the lowest (0.01) and highest (2.21) number of third instar larvae per fruit was collected on 11 December in Orland and on 5 October in San Diego in prerelease samples, respectively. Parasitoids were recovered from all release sites, the lowest (0.3%) and highest (100%) parasitism occurred on 25 January in Sylmar and on 26 October in Cayucos, respectively.
    [Show full text]