Global Gypsy-The Moth That Gets Around
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Aspects of the Biology of Entomogenous Fungi And
ASPECTS OF THE BIOLOGY OF ENTOMOGENOUS FUNGI AND THEIR ASSOCIATIONS WITH ARTHROPODS By EDUARDO MELITON JOVEL AYALA B.Sc. Agronomy, National School of Agriculture, El Salvador 1980 B.Sc. Botany, California State Polytechnic University, Pomona, California, USA 1993 M.Sc. Ethnobotany, University of British Columbia, Vancouver, Canada 1996 A THESIS SUBMITTED IN PARTIAL FULFILMENT OF THE REQUIREMENTS FOR THE DEGREE OF DOCTOR IN PHILOSOPHY In THE FACULTY OF GRADUATE STUDIES Department of Botany We accept this thesis as conforming to the required standards THE UNIVERSITY OF BRITISH COLUMBIA August 2002 © Eduardo M. Jovel Ayala, 2002 In presenting this thesis in partial fulfilment of the requirements for an advanced degree at the University of British Columbia, I agree that the Library shall make it freely available for reference and study. I further agree that permission for extensive copying of this thesis for scholarly purposes may be granted by the head of my department or by his or her representatives. It is understood that copying or publication of this thesis for financial gain shall not be allowed without my written permission. Department of The University of British Columbia Vancouver, Canada II ABSTRACT I investigated several aspects of the biology of entomogenous fungi (mostly Clavicipitaceae with few species of Hypocreaceae). My primary motive in this research was to gain an understanding of the interactions between entomogenous fungi and arthropods. My study included field collections and identification of entomogenous fungi from BC and a few collections from Peru and Idaho. I addressed some aspects of the interactions among arthropods and fungi, life histories of fungi under laboratory conditions, and observations of chemical changes of fungi growing in the presence of heavy metals. -
Supporting Information
Supporting Information Craft et al. 10.1073/pnas.0913084107 SI Materials and Methods Phylogenetic analysis of mitochondrial COI haplotypes con- Study Area, Caterpillars, and Host Plants. We outlined an approx- firmed the reciprocal monophyly of species and species complexes imately equidistant grid of eight sites with an average distance of (Fig. S1), but caution should be exercised when evaluating 160 km between neighboring sites and with pairwise distances phylogenetic relationships among species in community samples ranging from 59 to 513 km. Sites were located at <500 m above because of incomplete taxon sampling. Although the monophyly sea level in vegetation classified as mixed evergreen hill forest of Tortricidae and Thyrididae was recovered, a number of er- (1). The area has a human population of <10 people per km2 roneous groupings were evident; for example, Geometridae were and has <1 km of roads per 100 km2. The climate at these sites is nested within Crambidae, and Noctuidae were polyphyletic. humid, with a mean annual rainfall of 3,000–4,000 mm, a mod- Moreover, Gelechiidae relationships were unresolved, and the erate dry season from July to September (monthly mean rainfall, monophyly of three families represented by only single species <100 mm), and a mean monthly temperature of ∼26 °C. could not be assessed. Evolutionary interpretation of phyloge- The study area is situated in a complex tectonic region at the netic trends in dietary specialization and geographic distribution convergence of two major plates, the Australian and Pacific, where must be based not on Fig. S1, but rather on the best available ancient accretion of volcanic arc terranes to the central cordillera estimate of phylogeny, which necessarily is a synthesis of in- border the Sepik and Ramu river basins. -
Population Genetics of Ecological Communities with DNA Barcodes: an Example from New Guinea Lepidoptera
Population genetics of ecological communities with DNA barcodes: An example from New Guinea Lepidoptera Kathleen J. Crafta, Steffen U. Paulsb, Karolyn Darrowc, Scott E. Millerc, Paul D. N. Hebertd, Lauren E. Helgenc, Vojtech Novotnye, and George D. Weiblena,1 Departments of aPlant Biology and bEntomology, University of Minnesota, Saint Paul, MN 55108; cNational Museum of Natural History, Smithsonian Institution, Washington, DC 20013; dBiodiversity Institute of Ontario, University of Guelph, Guelph, ON N1G 2W1, Canada; and eInstitute of Entomology, Czech Academy of Sciences and Department of Zoology, University of South Bohemia, Branisovska 31, 370 05 Ceske Budejovice, Czech Republic Communicated by Hans R. Herren, Millennium Institute, Arlington, VA, January 5, 2010 (received for review November 23, 2008) Comparative population genetics of ecological guilds can reveal specialists, and may in fact confirm polyphagy (9). Population generalities in patterns of differentiation bearing on hypotheses genetic analyses of entire herbivorous insect communities are regarding the origin and maintenance of community diversity. needed to understand the extent of host-associated differ- Contradictory estimates of host specificity and beta diversity in entiation (10); no such studies have yet been reported in the tropical Lepidoptera (moths and butterflies) from New Guinea and tropics, however. the Americas have sparked debate on the role of host-associated Population genetic analyses also can test biogeographic divergence and geographic isolation in explaining -
Effects of Bacillus Thuringiensis
Long Term Evaluation of the Effects of Bacillus thuringiensis kurstaki, Gypsy Moth Nucleopolyhedrosis Virus Product Gypchek®, and Entomophaga maimaiga on Nontarget Organisms in Mixed Broadleaf-Pine Forests in the Central Appalachians John S. Strazanac and Linda Butler Editors Division of Plant and Soil Sciences West Virginia University Morgantown, West Virginia Authors Linda Butler Sandra Raimondo Division of Plant and Soil Sciences United States Environmental West Virginia University Protection Agency Morgantown, WV Gulf Breeze, FL Sandra B. Cederbaum Kenneth E. Rastall Daniel B. Warnell School of Forest Resources Department of Biology University of Georgia Wheeling Jesuit University Athens, GA Wheeling, WV Robert J. Cooper George E. Seidel Daniel B. Warnell School of Forest Resources Davis College of Agriculture, University of Georgia Animal Sciences and Consumer Sciences Athens, GA West Virginia University Morgantown, WV Jennifer A. DeCecco School of Forest Resources John S. Strazanac Pennsylvania State University Division of Plant and Soil Sciences University Park, PA West Virginia University Morgantown, WV George A. Gale The School of Bioresources and Technology William V. Sutton King MongKut's University of Technology Department of Biological Sciences Thonburi, Bangkok, Thailand Marshall University Huntington, WV Ann E. Hajek Department of Entomology Mark B. Watson Cornell University Natural Science and Ithaca, NY Mathematics Department University of Charleston Vicki Kondo Charleston, WV Division of Plant and Soil Sciences West Virginia University Michael M. Wheeler Morgantown, WV Department of Entomology Cornell University Matthew R. Marshall Ithaca, NY School of Forest Resources Pennsylvania State University Alan B. Williams University Park, PA Department of Fisheries and Wildlife Sciences Thomas K. Pauley Virginia Tech Department of Biological Sciences Blacksburg, VA Marshall University Huntington, WV 2 Additional Contributors Terry R. -
Appendix 1—Reviewers and Contributers
Appendix 1—Reviewers and Contributers The following individuals provided assistance, information, and review of this report. It could not have been completed without their cooperation. USDA APHIS-PPQ: D. Alontaga*, T. Culliney*, H. Meissner*, L. Newton* Hawai’i Department of Agriculture, Plant Industry Division: B. Kumashiro, C. Okada, N. Reimer University of Hawai’i: F. Brooks*, H. Spafford* USDA Forest Service: K. Britton*, S. Frankel* USDI Fish and Wildlife Service: D. Cravahlo Forest Research Institute Malaysia: S. Lee* 1 U.S. Department of the Interior, Geological Survey: L. Loope* Hawai’i Department of Land and Natural Resources, Division of Forestry and Wildlife: R. Hauff New Zealand Ministry for Primary Industries: S. Clark* Hawai’i Coordinating Group on Alien Pest Species: C. Martin* *Provided review comments on the draft report. 2 Appendix 2—Scientific Authorities for Chapters 1, 2, 3, and 5 Hypothenemus obscurus (F.) Kallitaxila granulatae (Stål) Insects Klambothrips myopori Mound & Morris Charaxes khasianus Butler Monema flavescens Walker Acizzia uncatoides (Ferris & Klyver) Neopithecops zalmora Butler Actias luna L. Nesopedronia dura Beardsley Adoretus sinicus (Burmeister) Nesopedronia hawaiiensis Beardsley Callosamia promethea Drury Odontata dorsalis (Thunberg) Ceresium unicolor White Plagithmysus bilineatus Sharp Chlorophorus annularis (F.) Quadrastichus erythrinae Kim Citheronia regalis Fabricus Scotorythra paludicola Butler Clastoptera xanthocephala Germ. Sophonia rufofascia Kuoh & Kuoh Cnephasia jactatana Walker Specularis -
Oecophoridae) in North America
VOLUME 61, NUMBER 3 165 Journal of the Lepidopterists’ Society 61(3), 2007, 165–171 FIRST REPORT OF OECOPHORA BRACTELLA (L.) (OECOPHORIDAE) IN NORTH AMERICA MERRILL A. PETERSON (MAP) Biology Department, Western Washington University, Bellingham, WA 98225, USA (e-mail: [email protected]) ERIC H. LAGASA (EHL) Washington State Department of Agriculture, Olympia, WA 98504, USA (e-mail: [email protected]) STEVEN PASSOA (SP) USDA, APHIS, PPQ, The Ohio State University, Museum of Biodiversity, 1315 Kinnear Rd., Columbus, OH 43212, USA (e-mail: [email protected]) GADEN S. ROBINSON (GSR) Department of Entomology, Natural History Museum, Cromwell Road, London SW7 5BD, UK (e-mail: [email protected]) AND DAVID HOLDEN (DH) Canadian Food Inspection Agency, 400 - 4321 Still Creek Drive, Burnaby, BC V5C 6S7 Canada (e-mail: [email protected] ABSTRACT. The first report of Oecophora bractella (L.) from North America is given, based on collection records from Washington and British Columbia. This species is found throughout Europe, but is generally rare to uncommon through most of its range. Larvae occur on rot- ting wood in association with certain fungi and are not expected to reach pest status. Adults were captured at nine locations, with the first record from Seattle, WA in 1998. This first record and some of the subsequent records are from sites immediately adjacent to or associated with in- ternational shipping routes. Other sites with O. bractella are from residential areas, two of which have established breeding populations. The introduction of this moth is surprising, particularly given the low interception rate at United States ports and its specialized feeding niche. -
Low Beta Diversity of Herbivorous Insects in Tropical Forests Vojtech Novotny, Scott E
doi: 10.1038/nature06021 SUPPLEMENTARY INFORMATION Low beta diversity of herbivorous insects in tropical forests Vojtech Novotny, Scott E. Miller, Jiri Hulcr, Richard A. I. Drew, Yves Basset, Milan Janda, Gregory P. Setliff, Karolyn Darrow, Alan J. A. Stewart, John Auga, Brus Isua, Kenneth Molem, Markus Manumbor, Elvis Tamtiai, Martin Mogia & George D. Weiblen Supplementary Material Supplementary Results Species distribution and host specificity The maximum possible geographic span for a particular herbivore species is a function of the combined distributions of all recorded hosts. It amounted to the entire 513 km span for all 76 Lepidoptera species analyzed. However, not all host species were sampled at all eight sites even when present, so the maximum geographic span we could observe for different Lepidoptera species ranged from 352 to 513 km (Supplementary Appendix S2). This maximum distribution was reached by 50 out of 76 Lepidoptera species while the remaining 26 species occupied 31 - 97% (median 88%) of the geographic span permitted by the distribution of their host plants. Supplementary Figures 0.4 0.3 0.2 Ü 0.1 - 1 1 1 1 1 0 100 200 300 400 500 Distance (km) Fig. SI. The probability C(d) that caterpillars are conspecific when randomly selected from the same host plant species at study sites separated by the distance J as a function of distance. Mean (± S.E.) values were calculated for caterpillar communities from 5-12 plant species sampled simultaneously at each pair of study sites. C(d) was not a fiuiction of distance (Pearson r, P>0.2). The intrasite C(d) where d= 0-5 km is shown but was not included in the correlation. -
Lepidoptera: Oecophoridae) in North America Merrill A
Western Washington University Western CEDAR Biology Faculty and Staff ubP lications Biology 2007 First report of Oecophora bractella (L.) (Lepidoptera: Oecophoridae) in North America Merrill A. Peterson Western Washington University, [email protected] Eric H. LaGasa Steven Passoa Gaden S. Robinson David Holden Follow this and additional works at: https://cedar.wwu.edu/biology_facpubs Part of the Biology Commons, and the Entomology Commons Recommended Citation Peterson, Merrill A.; LaGasa, Eric H.; Passoa, Steven; Robinson, Gaden S.; and Holden, David, "First report of Oecophora bractella (L.) (Lepidoptera: Oecophoridae) in North America" (2007). Biology Faculty and Staff Publications. 47. https://cedar.wwu.edu/biology_facpubs/47 This Article is brought to you for free and open access by the Biology at Western CEDAR. It has been accepted for inclusion in Biology Faculty and Staff ubP lications by an authorized administrator of Western CEDAR. For more information, please contact [email protected]. VOLUME 61, NUMBER 3 165 Journal of the Lepidopterists’ Society 61(3), 2007, 165–171 FIRST REPORT OF OECOPHORA BRACTELLA (L.) (OECOPHORIDAE) IN NORTH AMERICA MERRILL A. PETERSON (MAP) Biology Department, Western Washington University, Bellingham, WA 98225, USA (e-mail: [email protected]) ERIC H. LAGASA (EHL) Washington State Department of Agriculture, Olympia, WA 98504, USA (e-mail: [email protected]) STEVEN PASSOA (SP) USDA, APHIS, PPQ, The Ohio State University, Museum of Biodiversity, 1315 Kinnear Rd., Columbus, OH 43212, USA (e-mail: [email protected]) GADEN S. ROBINSON (GSR) Department of Entomology, Natural History Museum, Cromwell Road, London SW7 5BD, UK (e-mail: [email protected]) AND DAVID HOLDEN (DH) Canadian Food Inspection Agency, 400 - 4321 Still Creek Drive, Burnaby, BC V5C 6S7 Canada (e-mail: [email protected] ABSTRACT. -
Kyrgyz Republic
Forestry Department Food and Agriculture Organization of the United Nations Forest Health & Biosecurity Working Papers OVERVIEW OF FOREST PESTS KYRGYZ REPUBLIC January 2007 Forest Resources Development Service Working Paper FBS/21E Forest Management Division FAO, Rome, Italy Forestry Department Overview of forest pests - Kyrgyz Republic DISCLAIMER The aim of this document is to give an overview of the forest pest1 situation in the Kyrgyz Republic. It is not intended to be a comprehensive review. The designations employed and the presentation of material in this publication do not imply the expression of any opinion whatsoever on the part of the Food and Agriculture Organization of the United Nations concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. © FAO 2007 1 Pest: Any species, strain or biotype of plant, animal or pathogenic agent injurious to plants or plant products (FAO, 2004). ii Overview of forest pests - Kyrgyz Republic TABLE OF CONTENTS Introduction..................................................................................................................... 1 Forest pests...................................................................................................................... 2 Naturally regenerating forests..................................................................................... 2 Insects .................................................................................................................... -
The California Oak Disease and Arthropod (CODA) Database1
The California Oak Disease and Arthropod (CODA) Database1 Tedmund J. Swiecki2 Elizabeth A. Bernhardt2 Richard A. Arnold3 Abstract: The California Oak Disease and Arthropod (CODA) host index database is a compilation of information on agents that colonize or feed on oaks in California. Agents in the database include plant-feeding insects and mites, nematodes, microorganisms, viruses, and abiotic disease agents. CODA contains summarized information on hosts, agents, information sources, and the details of the host-agent interaction. Most of the 853 insect species in CODA are in the orders Lepidoptera, Coleoptera, Hymenoptera, and Homoptera. About 40 percent of the 378 species of fungi in CODA are pathogens. Of these, basidiomycete wood decay fungi have the most significant ecological impact. andowners and resource managers need to consider the effects of diseases Land arthropod pests on oaks when formulating management plans for oak woodlands or individual oaks. Over the past century, many different researchers have described a wide array of diseases and arthropods that affect oaks in California. However, the reports are found in numerous sources, many of which are not readily available to professionals involved with oak management in California. As part of a project to study the impacts of diseases and arthropods on California rangeland oaks (Swiecki and others 1990, 1991a, 1991b), we set out to compile the existing information on agents affecting oaks in California. Our goal was to organize this information in a format that was readily accessible and easy to update. We developed a computerized database, the California Oak Disease and Arthropod (CODA) Host Index (Swiecki and others 1996), to store and organize preexisting and new information on arthropods, microorganisms, and abiotic factors that affect oak health in California.