First Field Release of the Cape-Ivy Shoot Tip-Galling Fly Along the California Coast
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Evaluation of a Plant-Herbivore System In
EVALUATION OF A PLANT-HERBIVORE SYSTEM IN DETERMINING POTENTIAL EFFICACY OF A CANDIDATE BIOLOGICAL CONTROL AGENT, CORNOPS AQUATICUM FOR WATER HYACINTH, EICHHORNIA CRASSIPES A thesis submitted in fulfillment of the requirements for the degree of DOCTOR OF PHILOSOPHY of RHODES UNIVERSITY by ANGELA BOWNES December 2008 Abstract Water hyacinth, Eichhornia crassipes Mart. Solms-Laubach (Pontederiaceae), a free- floating aquatic macrophyte of Neotropical origin, was introduced into South Africa as an ornamental aquarium plant in the early 1900’s. By the 1970’s it had reached pest proportions in dams and rivers around the country. Due to the sustainability, cost efficiency and low environmental risk associated with biological control, this has been a widely used method in an attempt to reduce infestations to below the threshold where they cause economic and ecological damage. To date, five arthropod and one pathogen biocontrol agents have been introduced for the control of water hyacinth but their impact has been variable. It is believed that their efficacy is hampered by the presence of highly eutrophic systems in South Africa in which plant growth is prolific and the negative effects of herbivory are therefore mitigated. It is for these reasons that new, potentially more damaging biocontrol agents are being considered for release. The water hyacinth grasshopper, Cornops aquaticum Brüner (Orthoptera: Acrididae), which is native to South America and Mexico, was brought into quarantine in Pretoria, South Africa in 1995. Although the grasshopper was identified as one of the most damaging insects associated with water hyacinth in its native range, it has not been considered as a biocontrol agent for water hyacinth anywhere else in the world. -
Dube Nontembeko 2019.Pdf (2.959Mb)
UNDERSTANDING THE FITNESS, PREFERENCE AND PERFORMANCE OF SPECIALIST HERBIVORES OF THE SOUTHERN AFRICAN BIOTYPE OF CHROMOLAENA ODORATA (ASTERACEAE), AND IMPACTS ON PHYTOCHEMISTRY AND GROWTH RATE OF THE PLANT By NONTEMBEKO DUBE Submitted in fulfillment of the academic requirement of Doctorate of Philosophy In The Discipline of Entomology School of Life Sciences College of Agriculture, Engineering and Science University of KwaZulu-Natal Pietermaritzburg South Africa 2019 PREFACE The research contained in this thesis was completed by the candidate while based in the Discipline of Entomology, School of Life Sciences of the College of Agriculture, Engineering and Science, University of KwaZulu-Natal, Pietermaritzburg campus, South Africa, under the supervision of Dr Caswell Munyai, Dr Costas Zachariades, Dr Osariyekemwen Uyi and the guidance of Prof Fanie van Heerden. The research was financially supported by the Natural Resource Management Programmes of the Department of Environmental Affairs, and Plant Health and Protection of the Agricultural Research Council. The contents of this work have not been submitted in any form to another university and, except where the work of others is acknowledged in the text, the results reported are due to investigations by the candidate. _________________________ Signed: N. Dube (Candidate) Date: 08 August 2019 __________________________ Signed: C. Munyai (Supervisor) Date: 08August 8, 2019 ________________________________ Signed: C. Zachariades (Co-supervisor) Date: 08 August 2019 _________________________________ -
Non-Target Effects of Insect Biocontrol Agents and Trends in Host Specificity Since 1985
CAB Reviews 2016 11, No. 044 Non-target effects of insect biocontrol agents and trends in host specificity since 1985 Roy Van Driesche*1 and Mark Hoddle2 Address: 1 Department of Environmental Conservation, University of Massachusetts, Amherst, MA 01003-9285, USA. 2 Department of Entomology, University of California, Riverside, CA 92521, USA. *Correspondence: Roy Van Driesche, Email: [email protected] Received: 6 October 2016 Accepted: 7 November 2016 doi: 10.1079/PAVSNNR201611044 The electronic version of this article is the definitive one. It is located here: http://www.cabi.org/cabreviews © CAB International 2016 (Online ISSN 1749-8848) Abstract Non-target impacts of parasitoids and predaceous arthropods used for classical biological control of invasive insects include five types of impact: (1) direct attacks on native insects; (2) negative foodweb effects, such as competition for prey, apparent competition, or displacement of native species; (3) positive foodweb effects that benefited non-target species; (4) hybridization of native species with introduced natural enemies; and (5) attacks on introduced weed biocontrol agents. Examples are presented and the commonness of effects discussed. For the most recent three decades (1985–2015), analysis of literature on the host range information for 158 species of parasitoids introduced in this period showed a shift in the third decade (2005–2015) towards a preponderance of agents with an index of genus-level (60%) or species-level (8%) specificity (with only 12% being assigned a family-level or above index of specificity) compared with the first and second decades, when 50 and 40% of introductions had family level or above categorizations of specificity and only 21–27 (1985–1994 and 1995–2004, respectively) with genus or 1–11% (1985–1994 and 1995–2004, respectively) with species-level specificity. -
National Program 304 – Crop Protection and Quarantine
APPENDIX 1 National Program 304 – Crop Protection and Quarantine ACCOMPLISHMENT REPORT 2007 – 2012 Current Research Projects in National Program 304* SYSTEMATICS 1245-22000-262-00D SYSTEMATICS OF FLIES OF AGRICULTURAL AND ENVIRONMENTAL IMPORTANCE; Allen Norrbom (P), Sonja Jean Scheffer, and Norman E. Woodley; Beltsville, Maryland. 1245-22000-263-00D SYSTEMATICS OF BEETLES IMPORTANT TO AGRICULTURE, LANDSCAPE PLANTS, AND BIOLOGICAL CONTROL; Steven W. Lingafelter (P), Alexander Konstantinov, and Natalie Vandenberg; Washington, D.C. 1245-22000-264-00D SYSTEMATICS OF LEPIDOPTERA: INVASIVE SPECIES, PESTS, AND BIOLOGICAL CONTROL AGENTS; John W. Brown (P), Maria A. Solis, and Michael G. Pogue; Washington, D.C. 1245-22000-265-00D SYSTEMATICS OF PARASITIC AND HERBIVOROUS WASPS OF AGRICULTURAL IMPORTANCE; Robert R. Kula (P), Matthew Buffington, and Michael W. Gates; Washington, D.C. 1245-22000-266-00D MITE SYSTEMATICS AND ARTHROPOD DIAGNOSTICS WITH EMPHASIS ON INVASIVE SPECIES; Ronald Ochoa (P); Washington, D.C. 1245-22000-267-00D SYSTEMATICS OF HEMIPTERA AND RELATED GROUPS: PLANT PESTS, PREDATORS, AND DISEASE VECTORS; Thomas J. Henry (P), Stuart H. McKamey, and Gary L. Miller; Washington, D.C. INSECTS 0101-88888-040-00D OFFICE OF PEST MANAGEMENT; Sheryl Kunickis (P); Washington, D.C. 0212-22000-024-00D DISCOVERY, BIOLOGY AND ECOLOGY OF NATURAL ENEMIES OF INSECT PESTS OF CROP AND URBAN AND NATURAL ECOSYSTEMS; Livy H. Williams III (P) and Kim Hoelmer; Montpellier, France. * Because of the nature of their research, many NP 304 projects contribute to multiple Problem Statements, so for the sake of clarity they have been grouped by focus area. For the sake of consistency, projects are listed and organized in Appendix 1 and 2 according to the ARS project number used to track projects in the Agency’s internal database. -
Biological Control of Cape Ivy Project
Biological Control of Cape-ivy Project 2005-2006 Biennial Research Report prepared by Joe Balciunas and Chris Mehelis United States Department of Agriculture - Agricultural Research Service Western Regional Research Center - Exotic & Invasive Weed Research Unit 800 Buchanan St., Albany, California 94710 (510) 559-5975 FAX: (510) 559-5982 II Executive Summary by Dr. Joe Balciunas This is our second ‘electronic’ report, and most of you will receive our Biennial Report for 2005 and 2006 as PDF attachment to an email. We hope that this will make our report more easily accessible, since you may chose to store it on your hard disk. There are also a 58 pages of Appendices that supplement this report. They can be viewed / downloaded from our FTP dropbox at ftp://147.49.50.52/dropbox/Balciunas/. The good news is that by the end of 2006, we had reached the milestone of completing our host range testing of our two most promising potential biological control agents for Cape ivy, the gall fly, Parafreutreta regalis, and the stem-boring moth, Digitivalva delaireae. We have tested more than 80 species of plants, and neither of our candidate agents was able to complete development on anything other than their Cape ivy host.{See sections II & III] We have collated our results, and are preparing a formal ‘petition’ seeking permission to release both of these agents in the field. This ‘petition’ will be submitted to TAG during the second quarter of 2007. We hope to receive a positive recommendation from TAG within 6 months. The outlook for receiving a release permit from USDA-APHIS-PPQ has improved, but is still not clear. -
Biological Control of Cape Ivy Project 2004 Annual Research Report
Biological Control of Cape ivy Project 2004 Annual Research Report prepared by Joe Balciunas, Chris Mehelis, and Maxwell Chau, with contributions from Liamé van der Westhuizen and Stefan Neser Flowering Cape ivy overgrowing trees and native vegetation along California’s coast near Bolinas United States Department of Agriculture - Agricultural Research Service Western Regional Research Center - Exotic & Invasive Weed Research Unit 800 Buchanan St., Albany, California 94710 (510) 559-5975 FAX: (510) 559-5982 Executive Summary by Dr. Joe Balciunas This is our first attempt at an ‘electronic’ report, and most of you will receive our Annual Report for 2004 as PDF attachment to an email. We hope that this will make our report more easily accessible, since you may chose to store it on your hard disk. We made solid progress during 2004 towards our goal of completing our host range testing of our two most promising potential biological control agents for Cape ivy. We overcame a summertime ‘crash’ of our laboratory colonies, and by year’s end had strong colonies of both the gall fly, Parafreutreta regalis, and the stem-boring moth, Digitivalva delaireae. By the end of 2004, we had tested more than 80 species of plants, and neither of our candidate agents was able to complete development on anything other than their Cape ivy host. The single dark cloud has been the continuing downturn in external funds to support our Cape ivy research, especially that conducted by our cooperators in Pretoria, South Africa. While we have managed to maintain a small research effort there, our cooperators are no longer assisting us in our host range evaluations. -
Non-Target Effects of Insect Biocontrol Agents and Trends in Host Specificity Since 1985
CAB Reviews 2016 11, No. 044 Non-target effects of insect biocontrol agents and trends in host specificity since 1985 Roy Van Driesche*1 and Mark Hoddle2 Address: 1 Department of Environmental Conservation, University of Massachusetts, Amherst, MA 01003-9285, USA. 2 Department of Entomology, University of California, Riverside, CA 92521, USA. *Correspondence: Roy Van Driesche, Email: [email protected] Received: 6 October 2016 Accepted: 7 November 2016 doi: 10.1079/PAVSNNR201611044 The electronic version of this article is the definitive one. It is located here: http://www.cabi.org/cabreviews © CAB International 2016 (Online ISSN 1749-8848) Abstract Non-target impacts of parasitoids and predaceous arthropods used for classical biological control of invasive insects include five types of impact: (1) direct attacks on native insects; (2) negative foodweb effects, such as competition for prey, apparent competition, or displacement of native species; (3) positive foodweb effects that benefited non-target species; (4) hybridization of native species with introduced natural enemies; and (5) attacks on introduced weed biocontrol agents. Examples are presented and the commonness of effects discussed. For the most recent three decades (1985–2015), analysis of literature on the host range information for 158 species of parasitoids introduced in this period showed a shift in the third decade (2005–2015) towards a preponderance of agents with an index of genus-level (60%) or species-level (8%) specificity (with only 12% being assigned a family-level or above index of specificity) compared with the first and second decades, when 50 and 40% of introductions had family level or above categorizations of specificity and only 21–27 (1985–1994 and 1995–2004, respectively) with genus or 1–11% (1985–1994 and 1995–2004, respectively) with species-level specificity. -
Exploration for Olive Fruit Fly Parasitoids Across Africa Reveals Regional
www.nature.com/scientificreports OPEN Exploration for olive fruit fy parasitoids across Africa reveals regional distributions and dominance of closely associated parasitoids Xingeng Wang1,4*, Vaughn M. Walton1,5, Kim A. Hoelmer2,4, Charles H. Pickett3, Arnaud Blanchet2, Robert K. Straser1,6, Alan A. Kirk2 & Kent M. Daane1* The olive fruit fy, Bactrocera oleae, has been a key pest of olives in Europe and North America. We conducted the largest exploration for parasitoids associated with the fy across Sub-Saharan Africa (Kenya, Namibia, and South Africa) including some of the fy’s adjoining regions (Canary Islands, Morocco, Réunion Island and Tunisia). From Sub-Saharan regions, four braconids were collected: Bracon celer, Psytallia humilis, P. lounsburyi, and Utetes africanus. Results showed that their regional dominance was related to climate niches, with P. humilis dominant in hot semi-arid areas of Namibia, P. lounsburyi dominant in more tropical areas of Kenya, and U. africanus prevalent in Mediterranean climates of South Africa. Psytallia concolor was found in the Canary Islands, Morocco and Tunisian, and the Afrotropical braconid Diachasmimorpha sp. near fullawayi on Réunion Island. Furthermore, we monitored the seasonal dynamics of the fy and parasitoids in Cape Province of South Africa. Results showed that fruit maturity, seasonal variations in climates and interspecifc interactions shape the local parasitoid diversity that contribute to the low fy populations. The results are discussed with regard to ecological adaptations of closely associated parasitoids, and how their adaptations impact biocontrol. Exotic insect pests ofen thrive in their invaded regions due to the absence of specialist natural enemies and lack of efective indigenous natural enemies1,2. -
Abstracts / Proceedings
1 Proceedings California Exotic Pest Plant Council Symposiums Volume 6: 2000, 2001, 2002 Edited by Mike Kelly California Exotic Pest Plant Council 2 Disclaimer The views and opinions expressed in the articles making up the content of this publication do not necessarily reflect the position of the California Exotic Pest Plant Council. Other copies of this proceedings are available by sending $10 to: CalEPPC Attn: Proceedings 1442-A Walnut St. #462 Berkeley CA 94709 California Exotic Pest Plant Council can be reached by writing to Doug Johnson, Executive Director, at the address above or email: [email protected] Visit the CalEPPC web site at www.caleppc.org All rights reserved. No part of this publication may be reproduced, stored in a retrieval system or transmitted in any form or by any means, electronic, mechanical, photocopying, recording or otherwise without the prior written permission of the publisher. Copyright 2003 by the California Exotic Pest Plant Council Cover weed: Arundo donax (Giant reed) Printed in the United States of America First printing September 2003 Recommended sample citation. Brooks, M. 2001. The Role of Fire in Promoting Plant Invasions. In, M. Kelly, (ed.). Proceedings of the California Exotic Pest Plant Council Symposium. Vol. 6: 2000-2002. pp. 29–30. 3 Contents Papers Presented at the CalEPPC 2000 Symposium A Survey in South Africa for Insects with Potential as Biological Control Agents for Cape Ivy (Delairea odorata Lemaire) E. Grobbelaar,* J. Balciunas,*** O.C. Neser* and S. Neser**, *National Collection of Insects, Biosystematics Division, Plant Protection Research Inst., Agricultural Research Council, SOUTH AFRICA, **Weeds Research Div., PPRI, ARC, SOUTH AFRICA, ***Exotic & Invasive Weed Management Research Unit, USDA-ARS, Western Regional Research Center 16 The Role of Fire in Promoting Plant Invasions Matt Brooks, U.S. -
CALIFORNIA AGRICULTURE • VOLUME 65, NUMBER 1 Known from Pakistan (Wharton 1989)
REVIEW ARTICLE ▼ Biological controls investigated to aid management of olive fruit fl y in California by Kent M. Daane, Marshall W. Johnson, A B C Charles H. Pickett, Karen R. Sime, Xin-Geng Wang, Hannah Nadel, John W. Andrews Jr. and Kim A. Hoelmer The widespread and rapid establish ment of the olive fruit fl y in Califor nia required immediate changes in D E F integrated pest management (IPM) programs for olives. After fi nd ing that resident natural enemies did not provide adequate control, researchers began a worldwide search for parasitoids, with explora Parasitoids imported into California for quarantine studies include braconid parasitoids reared tion in the Republic of South Africa, from wild olive fruit fl y, (A)Psyttalia lounsburyi, (B) Bracon celer and (C) Utetes africanus, as well as braconid parasitoids reared on other fruit fl y species, including (D)Diachasmimorpha Namibia, India, China and other longicaudata, (E) D. kraussii and (F) Fopius arisanus. countries. Parasitoids were shipped to California, and most were studied which serve as reservoirs and contrib- the immature stages are protected from in quarantine to determine the best ute to the fl y’s reinvasion of treated most generalist predators. species for release. Two parasitoid orchards (Collier and Van Steenwyk Before the larva pupates, it creates species — Psyttalia lounsburyi and 2003). Classical biological control — the a thin window on the fruit surface importation of natural enemies from through which it may be exposed to Psyttalia humilis — are now be the pest’s home range — offers the best predators. If the fruit is still fi rm, the ing released throughout the state’s opportunity to economically suppress larva will often pupate inside. -
Systematic Database of Names
Systematic Database of Names by Allen L. Norrbom, Lynn E. Carroll, F. Christian Thompson, Ian M. White & Amnon Freidberg Genus ACANTHIOPHILUS Rioxoptilona Hendel 1914[2102]: 78, Trypeta vaga Wiedemann Acanthiophilus Becker 1908[374]: 136, Tetanocera walkeri Wol- (OD). [6600353] laston (OD). [6600182] Yunacantha Chen & Zia 1963[816]: 643, nigrolimbata Chen & Zia (OD). [6600366] REFS—Bezzi 1924[472]: 139 (key to 3 spp. (obsolete) [AF]); Erectovena Ito 1984[2416]: 59, Rioxoptilona speciosa Hendel Bezzi 1926[476]: 295 (key to 7 spp. (obsolete) [AF: South Africa]); (OD). [6600442] Hendel 1927[2108]: 203 (key to 2 spp. [PA]); Kapoor 1993[2600]: 56 Lenitovena Ito 1984[2416]: 52, Trypeta trigona Matsumura (OD). (key to 2 spp. [OR: India]). [6600441] Erektovena Ito 1984[2416]: 62, incosp. Erectovena Ito, by present astrophorus. Sri Lanka [OR]. revision. [6600909] Acanthiophilus astrophorus Hering 1939[2182]: 187.—Sri Lanka. Acanthineura Agassiz 1846[52]: 1, missp. Acanthonevra Macquart. Western: Colombo. LT / NMW. Lectotype designated by Hardy [6601016] 1968: 129. [6602422] Acanthoneura Schiner 1868[3316]: 228, missp. Acanthonevra brunneus. Ethiopia, e. Zaire, Uganda, Kenya [AF]. Macquart. [6600654] Acanthiophilus brunneus Munro 1934[3467]: 4.—Zaire. Kivu: Acanthonera Hardy 1977[1946]: 61, missp. Acanthonevra Mac- Burunga (1°30’S 29°18’E). HT / AMNH. [6603522] quart. [6600935] ciconia. Uganda, Kenya [AF]. Acanthiophilus ciconia Munro 1957[3510]: 1025.—Kenya. REFS—Shiraki 1933[4432]: 296, 307 ((Acanthoneura & Ri- Aberdare Range, Mt. Kinangop, 10000 ft. HT ? BMNH. oxoptilona) keys to 5 spp. [PA, OR: Japan, Korea & Taiwan]); [6603741] Malloch 1939[3137]: 431 ((Acanthoneura) key to 3 spp. (obsolete) coarctatus. Cameroon [AF]. [AU]); Hardy 1951[1922]: 170 ((Acanthoneura) key to 4 spp. -
Field Release of the Gall-Forming Fly, Parafreutreta Regalis Munro
United States Department of Agriculture Field Release of the Gall- Marketing and forming Fly, Parafreutreta Regulatory Programs regalis Munro (Diptera: Animal and Plant Health Tephritidae), for Inspection Service Biological Control of Cape-ivy, Delairea odorata (Asterales: Asteraceae), in the Contiguous United States Environmental Assessment, April 2016 Field Release of the Gall-forming Fly, Parafreutreta regalis Munro (Diptera: Tephritidae), for Biological Control of Cape-ivy, Delairea odorata (Asterales: Asteraceae), in the Contiguous United States Environmental Assessment, April 2016 Agency Contact: Robert Tichenor Regulations, Permits, and Manuals Plant Protection and Quarantine Animal and Plant Health Inspection Service U.S. Department of Agriculture 4700 River Road, Unit 133 Riverdale, MD 20737–1236 Non-Discrimination Policy The U.S. Department of Agriculture (USDA) prohibits discrimination against its customers, employees, and applicants for employment on the bases of race, color, national origin, age, disability, sex, gender identity, religion, reprisal, and where applicable, political beliefs, marital status, familial or parental status, sexual orientation, or all or part of an individual's income is derived from any public assistance program, or protected genetic information in employment or in any program or activity conducted or funded by the Department. (Not all prohibited bases will apply to all programs and/or employment activities.) To File an Employment Complaint If you wish to file an employment complaint, you must contact your agency's EEO Counselor (PDF) within 45 days of the date of the alleged discriminatory act, event, or in the case of a personnel action. Additional information can be found online at http://www.ascr.usda.gov/complaint_filing_file.html.