Invasion Biology and Lessons for Biological Control
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Alfalfa PMG 12 19 11
UC IPM Pest Management Guidelines: ALFALFA September 2010 Contents (Dates in parenthesis indicate when each topic was updated) Alfalfa Year-Round IPM Program Checklist (11/06) ........................................................................................................................ iv General Information Integrated Pest Management (11/06) ................................................................................................................................................... 1 Selecting the Field (11/06) ................................................................................................................................................................... 2 Transgenic Herbicide-Tolerant Alfalfa (11/06) ................................................................................................................................... 3 Biological Control (11/06) ................................................................................................................................................................... 5 Sampling with a Sweep Net (11/06) .................................................................................................................................................... 6 Crop Rotation (11/06) .......................................................................................................................................................................... 8 Aphid Monitoring (9/07) ..................................................................................................................................................................... -
ELIZABETH LOCKARD SKILLEN Diversity of Parasitic Hymenoptera
ELIZABETH LOCKARD SKILLEN Diversity of Parasitic Hymenoptera (Ichneumonidae: Campopleginae and Ichneumoninae) in Great Smoky Mountains National Park and Eastern North American Forests (Under the direction of JOHN PICKERING) I examined species richness and composition of Campopleginae and Ichneumoninae (Hymenoptera: Ichneumonidae) parasitoids in cut and uncut forests and before and after fire in Great Smoky Mountains National Park, Tennessee (GSMNP). I also compared alpha and beta diversity along a latitudinal gradient in Eastern North America with sites in Ontario, Maryland, Georgia, and Florida. Between 1997- 2000, I ran insect Malaise traps at 6 sites in two habitats in GSMNP. Sites include 2 old-growth mesic coves (Porters Creek and Ramsay Cascades), 2 second-growth mesic coves (Meigs Post Prong and Fish Camp Prong) and 2 xeric ridges (Lynn Hollow East and West) in GSMNP. I identified 307 species (9,716 individuals): 165 campoplegine species (3,273 individuals) and a minimum of 142 ichneumonine species (6,443 individuals) from 6 sites in GSMNP. The results show the importance of habitat differences when examining ichneumonid species richness at landscape scales. I report higher richness for both subfamilies combined in the xeric ridge sites (Lynn Hollow West (114) and Lynn Hollow East (112)) than previously reported peaks at mid-latitudes, in Maryland (103), and lower than Maryland for the two cove sites (Porters Creek, 90 and Ramsay Cascades, 88). These subfamilies appear to have largely recovered 70+ years after clear-cutting, yet Campopleginae may be more susceptible to logging disturbance. Campopleginae had higher species richness in old-growth coves and a 66% overlap in species composition between previously cut and uncut coves. -
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This article was downloaded by: [USDA National Agricultural Library] On: 1 October 2008 Access details: Access Details: [subscription number 790740294] Publisher Taylor & Francis Informa Ltd Registered in England and Wales Registered Number: 1072954 Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK Biocontrol Science and Technology Publication details, including instructions for authors and subscription information: http://www.informaworld.com/smpp/title~content=t713409232 A critical evaluation of host ranges of parasitoids of the subtribe Diabroticina (Coleoptera: Chrysomelidae: Galerucinae: Luperini) using field and laboratory host records Stefan Toepfer a; Guillermo Cabrera Walsh b; Astrid Eben c; Rebeca Alvarez-Zagoya d; Tim Haye a; Feng Zhang a; Ulrich Kuhlmann a a CABI Europe-Switzerland, Delémont, Switzerland b USDA ARS South American Biocontrol Laboratory, Hurlingham, Buenos Aires, Argentina c Departamento de Ecología Funcional, Instituto de Ecología, Xalapa, Veracruz, Mexico d Instituto Politécnico Nacional, CIIDR-IPN, Durango, Mexico Online Publication Date: 01 January 2008 To cite this Article Toepfer, Stefan, Cabrera Walsh, Guillermo, Eben, Astrid, Alvarez-Zagoya, Rebeca, Haye, Tim, Zhang, Feng and Kuhlmann, Ulrich(2008)'A critical evaluation of host ranges of parasitoids of the subtribe Diabroticina (Coleoptera: Chrysomelidae: Galerucinae: Luperini) using field and laboratory host records',Biocontrol Science and Technology,18:5,483 — 504 To link to this Article: DOI: 10.1080/09583150802001742 URL: http://dx.doi.org/10.1080/09583150802001742 PLEASE SCROLL DOWN FOR ARTICLE Full terms and conditions of use: http://www.informaworld.com/terms-and-conditions-of-access.pdf This article may be used for research, teaching and private study purposes. Any substantial or systematic reproduction, re-distribution, re-selling, loan or sub-licensing, systematic supply or distribution in any form to anyone is expressly forbidden. -
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(S): Diego J
Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States Author(s): Diego J. Inclan and John O. Stireman, III Source: Annals of the Entomological Society of America, 104(2):287-296. Published By: Entomological Society of America https://doi.org/10.1603/AN10047 URL: http://www.bioone.org/doi/full/10.1603/AN10047 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. CONSERVATION BIOLOGY AND BIODIVERSITY Tachinid (Diptera: Tachinidae) Parasitoid Diversity and Temporal Abundance at a Single Site in the Northeastern United States 1 DIEGO J. INCLAN AND JOHN O. STIREMAN, III Department of Biological Sciences, 3640 Colonel Glenn Highway, 235A, BH, Wright State University, Dayton, OH 45435 Ann. Entomol. Soc. Am. 104(2): 287Ð296 (2011); DOI: 10.1603/AN10047 ABSTRACT Although tachinids are one of the most diverse families of Diptera and represent the largest group of nonhymenopteran parasitoids, their local diversity and distribution patterns of most species in the family are poorly known. -
The Curculionoidea of the Maltese Islands (Central Mediterranean) (Coleoptera)
BULLETIN OF THE ENTOMOLOGICAL SOCIETY OF MALTA (2010) Vol. 3 : 55-143 The Curculionoidea of the Maltese Islands (Central Mediterranean) (Coleoptera) David MIFSUD1 & Enzo COLONNELLI2 ABSTRACT. The Curculionoidea of the families Anthribidae, Rhynchitidae, Apionidae, Nanophyidae, Brachyceridae, Curculionidae, Erirhinidae, Raymondionymidae, Dryophthoridae and Scolytidae from the Maltese islands are reviewed. A total of 182 species are included, of which the following 51 species represent new records for this archipelago: Araecerus fasciculatus and Noxius curtirostris in Anthribidae; Protapion interjectum and Taeniapion rufulum in Apionidae; Corimalia centromaculata and C. tamarisci in Nanophyidae; Amaurorhinus bewickianus, A. sp. nr. paganettii, Brachypera fallax, B. lunata, B. zoilus, Ceutorhynchus leprieuri, Charagmus gressorius, Coniatus tamarisci, Coniocleonus pseudobliquus, Conorhynchus brevirostris, Cosmobaris alboseriata, C. scolopacea, Derelomus chamaeropis, Echinodera sp. nr. variegata, Hypera sp. nr. tenuirostris, Hypurus bertrandi, Larinus scolymi, Leptolepurus meridionalis, Limobius mixtus, Lixus brevirostris, L. punctiventris, L. vilis, Naupactus cervinus, Otiorhynchus armatus, O. liguricus, Rhamphus oxyacanthae, Rhinusa antirrhini, R. herbarum, R. moroderi, Sharpia rubida, Sibinia femoralis, Smicronyx albosquamosus, S. brevicornis, S. rufipennis, Stenocarus ruficornis, Styphloderes exsculptus, Trichosirocalus centrimacula, Tychius argentatus, T. bicolor, T. pauperculus and T. pusillus in Curculionidae; Sitophilus zeamais and -
Diversification, Selective Sweep, and Body Size in the Invasive Palearctic
www.nature.com/scientificreports OPEN Diversifcation, selective sweep, and body size in the invasive Palearctic alfalfa weevil infected with Wolbachia Midori Tuda1,2,12*, Shun‑ichiro Iwase1,11,12, Khadim Kébé3,12, Julien Haran4,12, Jiri Skuhrovec5,12, Ehsan Sanaei6, Naomichi Tsuji7, Attila Podlussány8, Ottó Merkl8, Ahmed H. El‑Heneidy9 & Katsura Morimoto10 The alfalfa weevil Hypera postica, native to the Western Palearctic, is an invasive legume pest with two divergent mitochondrial clades in its invading regions, the Western clade and the Eastern/Egyptian clade. However, knowledge regarding the native populations is limited. The Western clade is infected with the endosymbiotic bacteria Wolbachia that cause cytoplasmic incompatibility in host weevils. Our aim was to elucidate the spatial genetic structure of this insect and the efect of Wolbachia on its population diversity. We analyzed two mitochondrial and two nuclear genes of the weevil from its native ranges. The Western clade was distributed in western/central Europe, whereas the Eastern/ Egyptian clade was distributed from the Mediterranean basin to central Asia. Intermediate mitotypes were found from the Balkans to central Asia. Most Western clade individuals in western Europe were infected with an identical Wolbachia strain. Mitochondrial genetic diversity of the infected individuals was minimal. The infected clades demonstrated a higher nonsynonymous/synonymous substitution rate ratio than the uninfected clades, suggesting a higher fxation of nonsynonymous mutations due to a selective sweep by Wolbachia. Trans‑Mediterranean and within‑European dispersal routes were supported. We suggest that the ancestral populations diversifed by geographic isolation due to glaciations and that the diversity was reduced in the west by a recent Wolbachia‑driven sweep(s). -
Barcoding Chrysomelidae: a Resource for Taxonomy and Biodiversity Conservation in the Mediterranean Region
A peer-reviewed open-access journal ZooKeys 597:Barcoding 27–38 (2016) Chrysomelidae: a resource for taxonomy and biodiversity conservation... 27 doi: 10.3897/zookeys.597.7241 RESEARCH ARTICLE http://zookeys.pensoft.net Launched to accelerate biodiversity research Barcoding Chrysomelidae: a resource for taxonomy and biodiversity conservation in the Mediterranean Region Giulia Magoga1,*, Davide Sassi2, Mauro Daccordi3, Carlo Leonardi4, Mostafa Mirzaei5, Renato Regalin6, Giuseppe Lozzia7, Matteo Montagna7,* 1 Via Ronche di Sopra 21, 31046 Oderzo, Italy 2 Centro di Entomologia Alpina–Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy 3 Museo Civico di Storia Naturale di Verona, lungadige Porta Vittoria 9, 37129 Verona, Italy 4 Museo di Storia Naturale di Milano, Corso Venezia 55, 20121 Milano, Italy 5 Department of Plant Protection, College of Agriculture and Natural Resources–University of Tehran, Karaj, Iran 6 Dipartimento di Scienze per gli Alimenti, la Nutrizione e l’Ambiente–Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy 7 Dipartimento di Scienze Agrarie e Ambientali–Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy Corresponding authors: Matteo Montagna ([email protected]) Academic editor: J. Santiago-Blay | Received 20 November 2015 | Accepted 30 January 2016 | Published 9 June 2016 http://zoobank.org/4D7CCA18-26C4-47B0-9239-42C5F75E5F42 Citation: Magoga G, Sassi D, Daccordi M, Leonardi C, Mirzaei M, Regalin R, Lozzia G, Montagna M (2016) Barcoding Chrysomelidae: a resource for taxonomy and biodiversity conservation in the Mediterranean Region. In: Jolivet P, Santiago-Blay J, Schmitt M (Eds) Research on Chrysomelidae 6. ZooKeys 597: 27–38. doi: 10.3897/ zookeys.597.7241 Abstract The Mediterranean Region is one of the world’s biodiversity hot-spots, which is also characterized by high level of endemism. -
Newsletter Dedicated to Information About the Chrysomelidae Report No
CHRYSOMELA newsletter Dedicated to information about the Chrysomelidae Report No. 55 March 2017 ICE LEAF BEETLE SYMPOSIUM, 2016 Fig. 1. Chrysomelid colleagues at meeting, from left: Vivian Flinte, Adelita Linzmeier, Caroline Chaboo, Margarete Macedo and Vivian Sandoval (Story, page 15). LIFE WITH PACHYBRACHIS Inside This Issue 2- Editor’s page, submissions 3- 2nd European Leaf Beetle Meeting 4- Intromittant organ &spermathecal duct in Cassidinae 6- In Memoriam: Krishna K. Verma 7- Horst Kippenberg 14- Central European Leaf Beetle Meeting 11- Life with Pachybrachis 13- Ophraella communa in Italy 16- 2014 European leaf beetle symposium 17- 2016 ICE Leaf beetle symposium 18- In Memoriam: Manfred Doberl 19- In Memoriam: Walter Steinhausen 22- 2015 European leaf beetle symposium 23- E-mail list Fig. 1. Edward Riley (left), Robert Barney (center) and Shawn Clark 25- Questionnaire (right) in Dunbar Barrens, Wisconsin, USA. Story, page 11 International Date Book The Editor’s Page Chrysomela is back! 2017 Entomological Society of America Dear Chrysomelid Colleagues: November annual meeting, Denver, Colorado The absence pf Chrysomela was the usual combina- tion of too few submissions, then a flood of articles in fall 2018 European Congress of Entomology, 2016, but my mix of personal and professional changes at July, Naples, Italy the moment distracted my attention. As usual, please consider writing about your research, updates, and other 2020 International Congress of Entomology topics in leaf beetles. I encourage new members to July, Helsinki, Finland participate in the newsletter. A major development in our community was the initiation of a Facebook group, Chrysomelidae Forum, by Michael Geiser. It is popular and connections grow daily. -
Proceedings of the United States National Museum
: BEETLE LARVAE OF THE SUBFAMILY GALERUCINAE B}^ Adam G. Boving Senior Entoniolotjist, Bureau of Etitomology, United States Department of Agricvltwe INTRODUCTION The present pajxn- is the result of a continued investigation of the Chrysomelid hirvae in the United States National Museum, Wash- ington, D. C. Of the subfamily Galerucinae ^ belonging to this family the larvae are preserved in the Museum of the following species Monocesta coryli Say. Trirhabda canadensis Kirby. TrU'habda hrevicollis LeConte. Trirhabda nitidicollis LeConte. Trirhabda tomentosa Linnaeus. Trirhabda attenuata Say. Oalerucella nymphaeae Liiniaeus. Oalerucella lineola Fabrleius (from Euroiie). Galerucclla sagittarUu' Gylleuhal. Oalerucella luteola Miiller. Galerucclla sp. (from Nanking, China). Galcrucella vibvrni Paykull (from Europe). Oalerucella decora Say. Oalerucella notata Fabricius. Oalerucella cribrata LeConte. Monoxia puncticolUs Say. Monoxia consputa LeConte. Lochmaca capreae Linnaeus (from Europe). Qaleruca tanacett Linnaeus (from Europe). Oaleruca laticollis Sahlberg (from Europe). Oalcruca, pomonae Scopoli. Sermylassa halensls Linnaeus. Agelastica alnl Linnaeus.^ 1 The generic and specific names of tlie North American larvae are as listed in C W. Leng's " Catalogue of Coleoptera of America north of Mexico, 1920," with corrections and additions as given in the "supplement" to the catalogue published by C. W. Leng and A. J. Mutchler, 1927. The European species, not introduced into North America, are named according to the " Catalogus Coleopterorum Europae, second edition, 1906," by L. V. Heyden, E. Rcitter, and .7. Weise. 2 It will be noticed that in the enumeration above no species of Dinhrlica and Pliyllo- brotica are mentioned. The larvae of those genera were considered by tlie present author as Halticinae larvae [Boving, Adam G. -
Biosecurity Risk Assessment
An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries RIRDC Publication No. 11/141 RIRDCInnovation for rural Australia An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries by Dr Robert C Keogh February 2012 RIRDC Publication No. 11/141 RIRDC Project No. PRJ-007347 © 2012 Rural Industries Research and Development Corporation. All rights reserved. ISBN 978-1-74254-320-8 ISSN 1440-6845 An Invasive Risk Assessment Framework for New Animal and Plant-based Production Industries Publication No. 11/141 Project No. PRJ-007347 The information contained in this publication is intended for general use to assist public knowledge and discussion and to help improve the development of sustainable regions. You must not rely on any information contained in this publication without taking specialist advice relevant to your particular circumstances. While reasonable care has been taken in preparing this publication to ensure that information is true and correct, the Commonwealth of Australia gives no assurance as to the accuracy of any information in this publication. The Commonwealth of Australia, the Rural Industries Research and Development Corporation (RIRDC), the authors or contributors expressly disclaim, to the maximum extent permitted by law, all responsibility and liability to any person, arising directly or indirectly from any act or omission, or for any consequences of any such act or omission, made in reliance on the contents of this publication, whether or not caused by any negligence on the part of the Commonwealth of Australia, RIRDC, the authors or contributors. The Commonwealth of Australia does not necessarily endorse the views in this publication. -
A Parasitoid of Diabrotica Virgifera Virgifera (Coleoptera: Chrysomelidae)
Bulletin of Entomological Research (2003) 93, 569–575 DOI: 10.1079/BER2003264 Basic biology and small-scale rearing of Celatoria compressa (Diptera: Tachinidae), a parasitoid of Diabrotica virgifera virgifera (Coleoptera: Chrysomelidae) F. Zhang, S. Toepfer and U. Kuhlmann* CABI Bioscience Switzerland Centre, Rue des Grillons 1, 2800 Delémont, Switzerland Abstract The tachinid Celatoria compressa Wulp has been evaluated as a candidate biological control agent for the western corn rootworm, Diabrotica virgifera virgifera LeConte, in Europe, where it is an invasive alien pest of maize. Special emphasis has been placed on understanding aspects of the parasitoid basic biology and on developing a rearing technique for a small-scale production of C. compressa puparia. The age of C. compressa adults was found to be the most crucial factor in achieving mating. Only newly emerged, 1-h-old females, mated successfully with 2- to 5-day-old males, achieving a success rate of 74%. After mating, a prelarviposi- tion period of 4 days occurred. The 5-day-old C. compressa females inserted their eggs containing fully-developed first instars directly into adults of D. v. virgifera. Total larval and pupal developmental time, including a pre-larviposition period of 4 days, was 29 days under quarantine laboratory conditions (25°C daytime, 15°C at night, L:D 14:10, 50% ± 10% r.h). Females of C. compressa were capable of producing on average 30 puparia throughout a female’s mean larviposition period of 15 days. A large number of host attacks by C. compressa were unsuccessful, resulting in a mean larviposition success rate of 24% per female. -
Oviposition by Pyrrhalta Viburni (Paykull) on Dead Plant Material: Successful Reproductive Strategy Or Maladaptive Behavior?1
Oviposition by Pyrrhalta viburni (Paykull) on dead plant material: successful reproductive strategy or maladaptive behavior?1 Gaylord A. Desurmont2, Charissa M. Fritzen3, and Paul A. Weston4 Abstract. Viburnum leaf beetle, Pyrrhalta viburni (Paykull, 1799), is a Eurasian chrysomelid recently introduced to North America, where it has become a major landscape pest. P. v ibur ni deposits eggs in the terminal twigs of infested viburnum shrubs, in small cavities that are then covered by the female with a frass-like secre- tion. In the fi eld, fresh P. v ibur ni egg masses are sometimes laid on dead plant mate- rial, prompting the current study to investigate the frequency and proximate causes of this behavior. In the fi eld, P. v ibur ni females were found to lay signifi cantly more eggs on live twigs than on dead twigs, and to lay more eggs on dead twigs that had been infested the previous growing season and contained remains of old egg masses than on non-infested dead twigs. In laboratory choice-tests, females laid signifi cantly more eggs on dead twigs if they contained remains of old egg masses, but did not show preferences between young and old infested twigs. We conclude that the pres- ence of remains of egg masses deposited the previous growing season is stimulatory to P. v ibur ni females and triggers oviposition on dead plant material. Keywords. Pyrrhalta viburni, oviposition behavior, insect-plant interactions, repro- ductive strategy, site selection. 1. Introduction Viburnum leaf beetle, Pyrrhalta viburni (Paykull, 1799), is a chrysomelid belonging to the subfamily Galerucinae and the tribe Galerucini.