BENEFICIALS – Predators, Parasitoids and Pathogens White Collared Ladybird
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Ancient Roaches Further Exemplify 'No Land Return' in Aquatic Insects
Gondwana Research 68 (2019) 22–33 Contents lists available at ScienceDirect Gondwana Research journal homepage: www.elsevier.com/locate/gr Ancient roaches further exemplify ‘no land return’ in aquatic insects Peter Vršanský a,b,c,d,1, Hemen Sendi e,⁎,1, Danil Aristov d,f,1, Günter Bechly g,PatrickMüllerh, Sieghard Ellenberger i, Dany Azar j,k, Kyoichiro Ueda l, Peter Barna c,ThierryGarciam a Institute of Zoology, Slovak Academy of Sciences, Dúbravská cesta 9, 845 06 Bratislava, Slovakia b Slovak Academy of Sciences, Institute of Physics, Research Center for Quantum Information, Dúbravská cesta 9, Bratislava 84511, Slovakia c Earth Science Institute, Slovak Academy of Sciences, Dúbravská cesta 9, P.O. BOX 106, 840 05 Bratislava, Slovakia d Paleontological Institute, Russian Academy of Sciences, Profsoyuznaya 123, 117868 Moscow, Russia e Faculty of Natural Sciences, Comenius University, Ilkovičova 6, Bratislava 84215, Slovakia f Cherepovets State University, Cherepovets 162600, Russia g Staatliches Museum für Naturkunde Stuttgart, Rosenstein 1, D-70191 Stuttgart, Germany h Friedhofstraße 9, 66894 Käshofen, Germany i Bodelschwinghstraße 13, 34119 Kassel, Germany j State Key Laboratory of Palaeobiology and Stratigraphy, Nanjing Institute of Geology and Palaeontology, Chinese Academy of Sciences, Nanjing 210008, PR China k Lebanese University, Faculty of Science II, Fanar, Natural Sciences Department, PO Box 26110217, Fanar - Matn, Lebanon l Kitakyushu Museum, Japan m River Bigal Conservation Project, Avenida Rafael Andrade y clotario Vargas, 220450 Loreto, Orellana, Ecuador article info abstract Article history: Among insects, 236 families in 18 of 44 orders independently invaded water. We report living amphibiotic cock- Received 13 July 2018 roaches from tropical streams of UNESCO BR Sumaco, Ecuador. -
The Seasonal Abundance and Impact of Predatory Arthropods on Helicoverpa Species in Australian Cotton Fields
The Seasonal Abundance and Impact of Predatory Arthropods on Helicoverpa Species in Australian Cotton Fields by John Newton Stanley B.Rur. Sc. (University of New England) A thesis submitted for the degree of Doctor of Philosophy from the University of New England Department of Agronomy and Soil Science September 1997 Many Thanks to the Following: Associate Professor Peter Gregg, who, as sole supervisor, provided a broad field of opportunities, as well as cotton, for the discovery of entomological things. Thank you for your guidance and support. Mr. Richard Browne, of Auscott Pty. Ltd., and Ben and Dave Coulton, of Coulton Farming Ltd. for allowing me access to their crops and for adjusting their cultural practices to accommodate experimental designs. Particular thanks to Terry Haynes (Senior Agronomist; Auscott Pty. Ltd. Moree) for discussions on pest management and generously supplying assistance at critical times. The taxonomists who identified material for the insect survey. Mr. L. Bauer (Thysanoptera) Dr. A. Calder (Coleoptera) Dr. M. Carver (Homoptera and Trichogrammatidae) Dr. D. H. Colless (Diptera) Dr. M. J. Fletcher (Cicadellidae) Dr. M. R. Gray (Aracnida) Dr. M. B. Malipatil (Hemiptera) Dr. I. D. Naumann (Hymenoptera) Dr. T. R. New (Neuroptera) Dr. T. A. Weir (Coleoptera) The people who provided technical assistance: Holly Ainslie, Dr. Steven Asante, Doreen Beness, Laura Bennett, Samantha Browne, Dr. Mark Coombs, Peter Foreman, Jacqueline Prudon, Sally Schwitzer, Kelly Stanley, Anita Stevenson, Donald Wheatley, and Richard Willis. Dr. Steven Trowell for guidance using serological methods and to Dr. Anne Bourne for her statistical significance. Mr. Robert Gregg for accomodating my family at Tyree whilst sampling in Moree. -
Why Hymenoptera – Not Coleoptera – Is the Most Speciose Animal Order
bioRxiv preprint doi: https://doi.org/10.1101/274431; this version posted March 22, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Quantifying the unquantifiable: 2 why Hymenoptera – not Coleoptera – is the most speciose animal order 3 4 Andrew A. Forbes, Robin K. Bagley, Marc A. Beer, Alaine C. Hippee, & Heather A. Widmayer 5 University of Iowa, Department of Biology, 434 Biology Building, Iowa City, IA 52242 6 7 Corresponding author: 8 Andrew Forbes 9 10 Email address: [email protected] 11 12 13 1 bioRxiv preprint doi: https://doi.org/10.1101/274431; this version posted March 22, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 14 Abstract 15 Background. We challenge the oft-repeated claim that the beetles (Coleoptera) are the most 16 species-rich order of animals. Instead, we assert that another order of insects, the Hymenoptera, 17 are more speciose, due in large part to the massively diverse but relatively poorly known 18 parasitoid wasps. The idea that the beetles have more species than other orders is primarily based 19 on their respective collection histories and the relative availability of taxonomic resources, which 20 both disfavor parasitoid wasps. Though it is unreasonable to directly compare numbers of 21 described species in each order, the ecology of parasitic wasps – specifically, their intimate 22 interactions with their hosts – allows for estimation of relative richness. -
Rainfall and Parasitic Wasp (Hymenoptera: Ichneumonoidea
Agricultural and Forest Entomology (2000) 2, 39±47 Rainfall and parasitic wasp (Hymenoptera: Ichneumonoidea) activity in successional forest stages at Barro Colorado Nature Monument, Panama, and La Selva Biological Station, Costa Rica B. A. Shapiro1 and J. Pickering Institute of Ecology, University of Georgia, Athens, GA 30602-2602, U.S.A. Abstract 1 In 1997, we ran two Malaise insect traps in each of four stands of wet forest in Costa Rica (two old-growth and two 20-year-old stands) and four stands of moist forest in Panama (old-growth, 20, 40 and 120-year-old stands). 2 Wet forest traps caught 2.32 times as many ichneumonoids as moist forest traps. The average catch per old-growth trap was 1.89 times greater than the average catch per second-growth trap. 3 Parasitoids of lepidopteran larvae were caught in higher proportions in the wet forest, while pupal parasitoids were relatively more active in the moist forest. 4 We hypothesize that moisture availability is of key importance in determining parasitoid activity, community composition and trophic interactions. Keywords Barro Colorado Nature Monument, Ichneumonoidea, La Selva, parasitoids, precipitation, tropical moist forest, tropical wet forest. istics of each parasitoid species and abiotic factors. Seasonal Introduction patterns of insect activity are often correlated with temperature, One of the largest groups of parasitic Hymenoptera is the as processes such as development and diapause are often superfamily Ichneumonoidea, which consists of two families intimately associated with temperature change (Wolda, 1988). (the Ichneumonidae and the Braconidae), 64 subfamilies and an Fink & VoÈlkl (1995) gave several examples of small insects for estimated 100 000 species world-wide (Gauld & Bolton, 1988; which low humidity and high temperature have detrimental Wahl & Sharkey, 1993). -
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. -
Predaceous Ground Beetles Caterpillar Hunters and Bombardier
E-185 5-03 PredaceousPredaceous GroundGround BeetBeetlesles Caterpillar Hunters and Bombardier Beetles Rick Minzenmayer, Extension Agent-IPM Chris Sansone, Extension Entomologist Texas Cooperative Extension redaceous ground beetles can be a nui- genus Calosoma, a brightly colored ground sance when numerous. They are beetle. Some species are called “bombardier PPattracted to lights and can sometimes beetles” because they emit what appears to be be found by the hundreds around lights in the smoke from the rear of the abdomen. The morning. The large numbers can also be a “smoke” is actually a glandular fluid that problem because the beetles defend them- vaporizes when it hits air; the fluid can irri- selves by emitting an odor. tate the skin. The ground beetles also emit an Ground beetles are part of the order odor to stop their enemies, including people. Coleoptera. This is the largest order of insects with over a quarter of a million species described throughout the world — about 30,000 species in the United States. Most beetles have two pairs of wings (elytra). The front pair is usually thickened and hard and meet in a straight line down the back when the wings are at rest. The back pair are mem- branous and folded beneath the front pair. All beetles have chewing mouthparts and under- go complete metamorphosis (egg, larva, pupa and adult). Predaceous ground beetles belong to the fami- ly Carabidae. This is the second largest family Caterpillar hunter, Calasoma scrutator (Fabricius) (Coleoptera: of beetles, with more than 2,500 species in Carabidae). North America. Most members of this family are considered beneficial, feeding on other insects in both the larval and adult stages. -
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). -
Classical Biological Control of Arthropods in Australia
Classical Biological Contents Control of Arthropods Arthropod index in Australia General index List of targets D.F. Waterhouse D.P.A. Sands CSIRo Entomology Australian Centre for International Agricultural Research Canberra 2001 Back Forward Contents Arthropod index General index List of targets The Australian Centre for International Agricultural Research (ACIAR) was established in June 1982 by an Act of the Australian Parliament. Its primary mandate is to help identify agricultural problems in developing countries and to commission collaborative research between Australian and developing country researchers in fields where Australia has special competence. Where trade names are used this constitutes neither endorsement of nor discrimination against any product by the Centre. ACIAR MONOGRAPH SERIES This peer-reviewed series contains the results of original research supported by ACIAR, or material deemed relevant to ACIAR’s research objectives. The series is distributed internationally, with an emphasis on the Third World. © Australian Centre for International Agricultural Research, GPO Box 1571, Canberra ACT 2601, Australia Waterhouse, D.F. and Sands, D.P.A. 2001. Classical biological control of arthropods in Australia. ACIAR Monograph No. 77, 560 pages. ISBN 0 642 45709 3 (print) ISBN 0 642 45710 7 (electronic) Published in association with CSIRO Entomology (Canberra) and CSIRO Publishing (Melbourne) Scientific editing by Dr Mary Webb, Arawang Editorial, Canberra Design and typesetting by ClarusDesign, Canberra Printed by Brown Prior Anderson, Melbourne Cover: An ichneumonid parasitoid Megarhyssa nortoni ovipositing on a larva of sirex wood wasp, Sirex noctilio. Back Forward Contents Arthropod index General index Foreword List of targets WHEN THE CSIR Division of Economic Entomology, now Commonwealth Scientific and Industrial Research Organisation (CSIRO) Entomology, was established in 1928, classical biological control was given as one of its core activities. -
Data Sheet on Helicoverpa
EPPO quarantine pest Prepared by CABI and EPPO for the EU under Contract 90/399003 Data Sheets on Quarantine Pests Helicoverpa zea IDENTITY Name: Helicoverpa zea (Boddie) Synonyms: Heliothis zea (Boddie) Bombyx obsoleta Fab. Phalaena zea (Boddie) Heliothis umbrosus Grote Taxonomic position: Insecta: Lepidoptera: Noctuidae Common names: American bollworm, corn earworm, tomato fruitworm, New World bollworm (English) Chenille des épis du maïs (French) Amerikanischer Baumwollkapselwurm (German) Notes on taxonomy and nomenclature: The taxonomic situation is complicated and presents several problems. Hardwick (1965) reviewed the New World corn earworm species complex and the Old World African bollworm (Noctuidae), most of which had previously been referred to as a single species (Heliothis armigera or H. obsoleta), and pointed out that there was a complex of species and subspecies involved. Specifically he proposed that the New World H. zea (first used in 1955) was distinct from the Old World H. armigera on the basis of male and female genitalia. And he described the new genus Helicoverpa to include these important pest species, Some 80 or more species were formerly placed in Heliothis (sensu lato) and Hardwick referred 17 species (including 11 new species) to Helicoverpa on the basis of differences in both male and female genitalia. Within this new genus the zea group contains eight species, and the armigera group two species with three subspecies. See also Hardwick (1970). Because the old name of Heliothis for the pest species (four major pest species and three minor) is so well established in the literature, and since dissection of genitalia is required for identification, there has been resistance to the name change (e.g. -
Parasites and Parasitoids Habitat and Conservation Host Specificity Diversity
Parasites and Parasitoids A parasitoid is a special type of parasite that is used in biological control. Unlike parasites, ALL parasitoids kill their host at some point during their development. This makes them very efficient at controlling various insect pests. Feeding by the larval parasitoid ultimately results in death of its host, and the resulting adult parasitoid is a free-living insect. Parasites, such as parasitic roundworms in humans, generally occur in very large numbers and do not kill their host. In many cases, tiny parasitoids are more effective at controlling pests than other larger predators. It is important to recognize their presence and needs to encourage good pest control Habitat and Conservation Most parasitoids are difficult to see because of their small size. Many times the only evidence you will see of their presence is a sick or dead pests that have already been parasitized. Adult parasitoids usually feed on pollen and require a source of food in order to lay eggs and kill their hosts. Broad spectrum pesticides applied to pest insects often kill these beneficial parasitoids. This is why it is important to reduce or eliminate harsh pesticides and encourage parasitoids by planting wild flowers near your crops. Host specificity Unlike generalist predators such as lady beetles and lacewings, parasitoids tend to be very host specific. This makes them good candidates for classical biological control of invasive species. In such examples, parasitoids can be imported without concern of non-target effects. To the left is a picture of a Larra parasitoid wasp which attacks only mole crickets. -
The Biology of Casmara Subagronoma (Lepidoptera
insects Article The Biology of Casmara subagronoma (Lepidoptera: Oecophoridae), a Stem-Boring Moth of Rhodomyrtus tomentosa (Myrtaceae): Descriptions of the Previously Unknown Adult Female and Immature Stages, and Its Potential as a Biological Control Candidate Susan A. Wineriter-Wright 1, Melissa C. Smith 1,* , Mark A. Metz 2 , Jeffrey R. Makinson 3 , Bradley T. Brown 3, Matthew F. Purcell 3, Kane L. Barr 4 and Paul D. Pratt 5 1 USDA-ARS Invasive Plant Research Laboratory, Fort Lauderdale, FL 33314, USA; [email protected] 2 USDA-ARS Systematic Entomology Lab, Beltsville, MD 20013-7012, USA; [email protected] 3 USDA-ARS Australian Biological Control Laboratory, CSIRO Health and Biosecurity, Dutton Park QLD 4102, Australia; jeff[email protected] (J.R.M.); [email protected] (B.T.B.); [email protected] (M.F.P.) 4 USDA-ARS Center for Medical, Agricultural and Veterinary Entomology, Gainesville, FL 32608, USA; [email protected] 5 USDA-ARS, Western Regional Research Center, Invasive Species and Pollinator Health Research Unit, 800 Buchanan Street, Albany, CA 94710, USA; [email protected] * Correspondence: [email protected]; Tel.: +1-954-475-6549 Received: 27 August 2020; Accepted: 16 September 2020; Published: 23 September 2020 Simple Summary: Rhodomyrtus tomentosa is a perennial woody shrub throughout Southeast Asia. Due to its prolific flower and fruit production, it was introduced into subtropical areas such as Florida and Hawai’i, where it is now naturalized and invasive. In an effort to find sustainable means to control R. tomentosa, a large-scale survey was mounted for biological control organisms. -
Autographa Gamma
1 Table of Contents Table of Contents Authors, Reviewers, Draft Log 4 Introduction to the Reference 6 Soybean Background 11 Arthropods 14 Primary Pests of Soybean (Full Pest Datasheet) 14 Adoretus sinicus ............................................................................................................. 14 Autographa gamma ....................................................................................................... 26 Chrysodeixis chalcites ................................................................................................... 36 Cydia fabivora ................................................................................................................. 49 Diabrotica speciosa ........................................................................................................ 55 Helicoverpa armigera..................................................................................................... 65 Leguminivora glycinivorella .......................................................................................... 80 Mamestra brassicae....................................................................................................... 85 Spodoptera littoralis ....................................................................................................... 94 Spodoptera litura .......................................................................................................... 106 Secondary Pests of Soybean (Truncated Pest Datasheet) 118 Adoxophyes orana ......................................................................................................