An Overview of Biological Control of Weeds in Tasmania
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Protection of Pandora Moth (Coloradia Pandora Blake) Eggs from Consumption by Golden-Mantled Ground Squirrels (Spermophilus Lateralis Say)
AN ABSTRACT OF THE THESIS OF Elizabeth Ann Gerson for the degree of Master of Science in Forest Science presented on 10 January, 1995. Title: Protection of Pandora Moth (Coloradia pandora Blake) Eggs From Consumption by Golden-mantled Ground Squirrels (Spermophilus lateralis Say) Abstract approved: Redacted for Privacy William C. McComb Endemic populations of pandora moths (Coloradia pandora Blake), a defoliator of western pine forests, proliferated to epidemic levels in central Oregon in 1986 and increased dramatically through 1994. Golden-mantled ground squirrels (Spermophilus lateralis Say) consume adult pandora moths, but reject nutritionally valuable eggs from gravid females. Feeding trials with captive S. lateralis were conducted to identify the mode of egg protection. Chemical constituents of fertilized eggs were separated through a polarity gradient of solvent extractions. Consumption of the resulting hexane, dichloromethane, and water egg fractions, and the extracted egg tissue residue, was evaluated by randomized 2-choice feeding tests. Consumption of four physically distinct egg fractions (whole eggs, "whole" egg shells, ground egg shells, and egg contents) also was evaluated. These bioassays indicated that C. pandora eggs are not protected chemically, however, the egg shell does inhibit S. lateralis consumption. Egg protection is one mechanism that enables C. pandora to persist within the forest food web. Spermophilus lateralis, a common and often abundant rodent of central Oregon pine forests, is a natural enemy of C. pandora -
The Insect Fauna Associated with Horehound (Marrubium Vulgare L
Plant Protection Quarterly Vol.15(1) 2000 21 belonging to eight orders were found feeding on the plant (Figure 2, Table 2). The insect fauna associated with horehound The insects included 12 polyphagous spe- (Marrubium vulgare L.) in western Mediterranean cies (44%), 8 oligophagous species (30%) and 7 monophagous species (26%). At the Europe and Morocco: potential for biological control larval stage, there were five root-feeding in Australia species (22%), one stem-boring species (4%), nine leaf-feeding species (39%), eight flower, ovary or seed feeding species A Jean-Louis Sagliocco , Keith Turnbull Research Institute, Victorian (34%). Based on adult feeding behaviour Department of Natural Resources and Environment, CRC for Weed there was one root-boring species (74%), Management Systems, PO Box 48, Frankston, Victoria 3199, Australia. six leaf-feeding species (40%) and eight A Previous address: CSIRO European Laboratory, Campus International de species feeding on flowers or ovaries or Baillarguet, 34980 Montferrier sur Lez, Cedex, France. seeds (53%). Wheeleria spilodactylus (Curtis) Summary were preserved. Immature stages were (Lepidoptera: Pterophoridae) Marrubium vulgare L. (Lamiaceae) was kept with fresh plant material until the Wheeleria spilodactylus was abundant at surveyed in western Mediterranean Eu- adult stage for identification. Insects most sites in France and Spain, and had rope and Morocco to identify the phy- were observed either in the field or the been recorded feeding on M. vulgare tophagous insect fauna associated with laboratory to confirm that they fed on the (Gielis 1996) and Ballota nigra (Bigot and this weed and to select species having plant. Insects were sent to museum spe- Picard 1983). -
The Winter Moth ( Operophtera Brumata) and Its Natural Enemies in Orkney
Spatial ecology of an insect host-parasitoid-virus interaction: the winter moth ( Operophtera brumata) and its natural enemies in Orkney Simon Harold Submitted in accordance with the requirements for the degree of Doctor of Philosophy The University of Leeds Faculty of Biological Sciences September 2009 The candidate confirms that the work submitted is his own and that appropriate credit has been given where reference has been made to the work of others This copy has been supplied on the understanding that it is copyright material and that no quotation from the thesis may be published without proper acknowledgement ©2009 The University of Leeds and Simon Harold ii Acknowledgements I gratefully acknowledge the support of my supervisors Steve Sait and Rosie Hails for their continued advice and support throughout the duration of the project. I particularly thank Steve for his patience, enthusiasm, and good humour over the four years—and especially for getting work back to me so quickly, more often than not because I had sent it at the eleventh hour. I would also like to express my gratitude to the Earth and Biosphere Institute (EBI) at the University of Leeds for funding this project in the first instance. Steve Carver also helped secure funding. The molecular work was additionally funded by both a NERC short-term grant, and funding from UKPOPNET, to whom I am also grateful. None of the fieldwork, and indeed the scope and scale of the project, would have been possible if not for the stellar cast of fieldworkers that made the journey to Orkney. They were (in order of appearance): Steve Sait, Rosie Hails, Jackie Osbourne, Bill Tyne, Cathy Fiedler, Ed Jones, Mike Boots, Sandra Brand, Shaun Dowman, Rachael Simister, Alan Reynolds, Kim Hutchings, James Rosindell, Rob Brown, Catherine Bourne, Audrey Zannesse, Leo Graves and Steven White. -
NEWSLETTER• of the MICHIGAN ENTOMOLOGICAL SOCIETY
NEWSLETTER• of the MICHIGAN ENTOMOLOGICAL SOCIETY Volume 38, Numbers 4 December, 1993 Impacts ofBt on Non-Target Lepidoptera John W. Peacock, David L. Wagner, and Dale F. Schweitzer USDA Forest Service, Hamden, CT; University of Connecticut, Storrs, CT; and The Nature Conservancy, Port Norris, NT, respectively Introduction gypsy moth in Oregon. Sample et a1. ing attempts bycertain birds. In another (1 993) have likewise reported a signifi study, Bellocq et al. (1992) showed that Bacillus thuringiensis Berliner var. cant reduction inspecies abundance and the use of Btk increased immigration kurstaki (Btk) is one of the pesticides richness in non-target Lepidoptera in rates andcaused d ietary shifts inshrews. most commonly employed against lepi field studies in eastern West Virginia. We report here a summary of our dopteran forest pests. In the eastern U.S., James et al. (1993) haveshown thatBtk is studies aimed at determining the effect where millionsofhectares of deciduous toxic to late, but not early, instar larvae of Btko n non-target Lepidoptera inboth forest have been defoliated by the ''Eu of the beneficial cinnabar moth, Tyria laboratoryand field studies. Laboratory ropean" gypsy moth, Lymantria dispar jacobaeae (L.). bioassays were conducted on larvae in (L.), Btk has been used extenSively to In addition to its direct effects on seven families of native eastern U.S. slow the spread of this pest and to re native Lepidoptera, Btk can indirectly Macrolepidoptera. Field studies were duce defoliation. In 1992 alone, over affect other animals that rely on lepi carried out in Rockbridge County, Vir 300,000 ha were treated with Btk, in dopterous larvae as a primary source of ginia, and were the first to evaluate non cluding gypsy moth suppression activi food. -
And Ragwort Flea Beetle, Cinnabar Moths and Other Organisms That Feed on Ragwort
Copyright is owned by the Author of the thesis. Permission is given for a copy to be downloaded by an individual for the purpose of research and private study only. The thesis may not be reproduced elsewhere without the permission of the Author. Interaction of population processes in ragwort (Senecio jacobaea L.) and ragwort flea.bee tle (Longitarsus jacobaeae Waterbouse) A Thesis presented in partial fulflllment of the requirements for the Degree of Doctor of Philosophy in Ecology at Massey University. April 2000 11 Declaration of Originality This thesis represents the original work of the author, except where otherwise acknowledged. It has not been submitted previously for a degree at any University. Aung Kyi III Acknowledgements I am sincerely grateful to my supervisors, Professor Brian Springett, Dr lan Stringer (Ecology, the Institute of Natural Resources, Massey University), and Dr Peter McGregor (Landcare Research) for their encouragement, supervision and patience over this study and their help in drafting this thesis. I am also indebted to Mr Keith Betteridge (AgResearch) for his valuable advice on the laboratory study on the movement of first instar larvae of ragwort flea beetle in different soils; Dr. Ed Minot (Ecology, Massey University) for explaining how to use the STELLA model; Dr. Jill Rapson (Ecology, Massey University) for comments on my PhD thesis proposal; Dr. Siva Ganesh, Dr. Jenny Brown and Mr. Duncan Hedderley (Statistics, Massey University) for help with univariate and multivariate analyses; and Dr. Kerry Harrington (Plant Science, Institute of Natural Resources, Massey University) for his comments and suggestion on the toxicity of ragwort and its chemical control. -
Developing Host Range Testing for Cotesia Urabae
1 Appendix 2 Appendix 2: Risks to non-target species from potential biological control agent Cotesia urabae against Uraba lugens in New Zealand L.A. Berndt, A. Sharpe, T.M. Withers, M. Kimberley, and B. Gresham Scion, Private Bag 3020, Rotorua 3046, New Zealand, [email protected] Introduction Biological control of insect pests is a sustainable approach to pest management that seeks to correct ecological imbalances that many new invaders create on arrival in a new country. This is done by introducing carefully selected natural enemies of the pest, usually from its native range. This method is the only means of establishing and maintaining self-sustaining control of pest insects and it is highly cost effective in the long term (Greathead, 1995). However there is considerable concern for the risk new biological control agents might pose to other species in the country of introduction, and most countries now have regulations to manage decisions on whether to allow biological control introductions (Sheppard et al., 2003). A key component of the research required to gain approval to release a new agent is host range testing, to determine what level of risk the agent might pose to native and valued species in the country of introduction. Although methods for this are well developed for weed biological control, protocols are less established for arthropod biological control, and the challenges in conducting tests are greater (Van Driesche and Murray, 2004; van Lenteren et al., 2006; Withers and Browne, 2004). This is because insect ecology and taxonomy are relatively poorly understood, and there are many more species that need to be considered. -
Building Expertise on Animal Defense Mechanisms
Grade 4: Module 2B: Unit 1: Lesson 5 Reading Scientific Text: Building Expertise on Animal Defense Mechanisms This work is licensed under a Creative Commons Attribution-NonCommercial-ShareAlike 3.0 Unported License. Exempt third-party content is indicated by the footer: © (name of copyright holder). Used by permission and not subject to Creative Commons license. GRADE 4: MODULE 2B: UNIT 1: LESSON 5 Reading Scientific Text: Building Expertise on Animal Defense Mechanisms Long-Term Targets Addressed (Based on NYSP12 ELA CCLS) I can paraphrase portions of a text that is read aloud to me. (SL.4.2) I can interpret information presented through charts or graphs. I can explain how that information helps me understand the text around it. (RI.4.7) I can determine the main idea using specific details from the text. (RI.4.2) Supporting Learning Targets Ongoing Assessment • I can paraphrase information presented in a read-aloud on animal defense mechanisms. • Listening Closely note-catcher (page 7 of Animal • I can make inferences about animal defense mechanisms by examining articles that include text and Defenses research journal) visuals. • Examining Visuals note-catcher (page 8 of Animal • I can determine the main idea of a section of Animal Behaviors: Animal Defenses. Defenses research journal) • Determining Main Ideas note-catcher (pages 9 and 10 of Animal Defenses research journal) • Observation of participation during Jigsaw Copyright © 2013 by Expeditionary Learning, New York, NY. All Rights Reserved. NYS Common Core ELA Curriculum • G4:M2B:U1:L5 • June 2014 • 1 GRADE 4: MODULE 2B: UNIT 1: LESSON 5 Reading Scientific Text: Building Expertise on Animal Defense Mechanisms Agenda Teaching Notes 1. -
Long-Term Changes to the Frequency of Occurrence of British Moths Are Consistent with Opposing and Synergistic Effects of Climate and Land-Use Changes
Journal of Applied Ecology 2014, 51, 949–957 doi: 10.1111/1365-2664.12256 Long-term changes to the frequency of occurrence of British moths are consistent with opposing and synergistic effects of climate and land-use changes Richard Fox1*, Tom H. Oliver2, Colin Harrower2, Mark S. Parsons1, Chris D. Thomas3 and David B. Roy2 1Butterfly Conservation, Manor Yard, Wareham, Dorset, BH20 5QP, UK; 2NERC Centre for Ecology & Hydrology, Maclean Building, Benson Lane, Crowmarsh Gifford, Wallingford, Oxfordshire, OX10 8BB, UK; and 3Department of Biology, University of York, York, YO10 5DD, UK Summary 1. Species’ distributions are likely to be affected by a combination of environmental drivers. We used a data set of 11 million species occurrence records over the period 1970–2010 to assess changes in the frequency of occurrence of 673 macro-moth species in Great Britain. Groups of species with different predicted sensitivities showed divergent trends, which we interpret in the context of land-use and climatic changes. 2. A diversity of responses was revealed: 260 moth species declined significantly, whereas 160 increased significantly. Overall, frequencies of occurrence declined, mirroring trends in less species-rich, yet more intensively studied taxa. 3. Geographically widespread species, which were predicted to be more sensitive to land use than to climate change, declined significantly in southern Britain, where the cover of urban and arable land has increased. 4. Moths associated with low nitrogen and open environments (based on their larval host plant characteristics) declined most strongly, which is also consistent with a land-use change explanation. 5. Some moths that reach their northern (leading edge) range limit in southern Britain increased, whereas species restricted to northern Britain (trailing edge) declined significantly, consistent with a climate change explanation. -
Identifying and Managing Common Groundsel (Senecio Vulgaris L.) In
MSU Extension Bulletin E3440 Identifying and managing common groundsel (Senecio vulgaris L.) in nurseries and greenhouses Debalina Saha and Carolyn Fitzgibbon Michigan State University Department of Horticulture Debalina Saha, MSU Horticulture Photo 1. Common groundsel (Senecio vulgaris) growing along the edges of walkway inside a greenhouse. Common groundsel (Senecio vulgaris) is one of the most common and problematic broadleaf Debalina Saha, MSU Horticulture weeds in nurseries and greenhouses. It belongs Photo 2. Erect and branched growth habit of common to the Asteraceae family, which also includes groundsel (Senecio vulgaris). dandelion, thistles and sunflower. It is classified identify and manage common groundsel in their as a winter annual because the seeds germinate nurseries and greenhouse operations. in late fall through early spring. Sometimes common groundsel is considered a summer annual since it has the capacity to germinate Biology of common groundsel under shady conditions in summer or fall. In addition to its general weediness, common HABITAT groundsel can be toxic to cattle, swine and Common groundsel can be found growing in horses if ingested. The toxicity is due to pyr- gardens, lawns, nursery plots, inside greenhous- rolizidine alkaloids, which can cause chronic es (under benches and on edges of walkways) liver damage to these animals (Smith-Fiola and (Photo 1), edges of yards, mulched beds around Gill, 2014; Uva et al., 1997). shrubs, fields, areas along railroads, roadsides The success of this weed lies with its ability to and waste areas. It is common in highly dis- produce enormous amount of seeds. Seed turbed areas where ground vegetation is low development starts early in its life cycle and and scant (Illinois wildflowers, 2020). -
Tansy Ragwort
United States Department of Agriculture NATURAL RESOURCES CONSERVATION SERVICE Invasive Species Technical Note No. MT-24 June 2009 Ecology and Management of Tansy Ragwort (Senecio jacobaea L.) By Jim Jacobs, Invasive Species Specialist and Plant Materials Specialist NRCS, Bozeman, Montana Sharlene Sing, Research Entomologist USFS Rocky Mountain Research Station, Bozeman, Montana Figure 1. A tansy ragwort infested pasture. Photo by Eric Coombs, Oregon Department of Agriculture, available from Bugwood.org Abstract Tansy ragwort, a member of the Asteraceae taxonomic family, is a large biennial or short-lived perennial herb native to and widespread throughout Europe and Asia. Stems can grow to a height of 5.5 feet (1.75 meters), with the lower half simple and the upper half many-branched at the inflorescence. Reproductive stems produce up to 2,500 bright golden-yellow flowers. Capitula (flowerheads) arranged in 20-60 flat-topped, dense corymbs per plant are composed of ray and disc florets; both produce achenes containing a single seed. Rosettes formed of distinctive pinnately-lobed leaves attain a diameter of up to 1.5 feet (0.5 meter). First reported in Montana in 1979 in Mineral County, tansy ragwort has since spread into Flathead, Lincoln, and Sanders Counties. Soils with medium to light textures in areas receiving sufficient rainfall (34 inches or 860 millimeters/year) readily support populations of tansy ragwort. This species is a troublesome weed in decadent pastures, waste areas, clear-cuts and along roadsides. Tansy ragwort produces pyrrolizidine alkaloids - these can be lethal if ingested by cattle, horses and deer, but are less toxic to sheep and goats. -
Staff Assessment Report
Staff Assessment Report APP203542: An application to release two moths (Wheeleria spilodactylus and Chamaesphecia mysiniformis) as biological control agents for the weed horehound (Marrubium vulgare). August 2018 To introduce two moths, Wheeleria spilodactylus and Chamaesphecia mysiniformis to Purpose control the weed horehound (Marrubium vulgare). APP203542 Application number Notified, Full Release Application type Horehound Biocontrol Group Applicant 15 May 2018 Date formally received 2 EPA advice for application APP203542 Executive Summary and Recommendation In May 2018, the Horehound Biocontrol Group made an application to the Environmental Protection Authority (EPA) seeking to introduce two moths, Wheeleria spilodactylus (the plume moth) and Chamaesphecia mysiniformis (the clearwing moth), as biological control agents for the weed horehound (Marrubium vulgare). We assessed the benefits (positive effects) and risks and costs (adverse effects) of introducing the two biocontrol agents to New Zealand and found that the benefits relating to environmental outcomes to be significant and the adverse effects negligible (Kaser & Ode 2016). We consider it likely that biological control of horehound will improve biodiversity values and conservation of protected natural habitats. We also consider it highly likely that biocontrol of horehound will reduce the costs of farming relating to crop replacement and wool processing. We note that this biocontrol programme could reduce the dispersal of the weed into sensitive environments. We consider it highly improbable for the plume moth and the clearwing moth to pose risks to native or valued plants in New Zealand. There are no native species in the Marrubium genus and, no other valued species within this genus in New Zealand. Host range experiments confirmed their narrow host specificity. -
Tansy Ragwort Removal
Tansy Ragwort Control Program Cedar River Municipal Watershed 1999 – 2017 Sally Nickelson Watershed Management Division Seattle Public Utilities December 20, 2017 Table of Contents INTRODUCTION......................................................................................................................... 1 LEGAL DESIGNATION ................................................................................................................... 1 LIFE HISTORY ............................................................................................................................... 1 SIMILAR SPECIES .......................................................................................................................... 2 BIOLOGICAL CONTROL ................................................................................................................. 3 OBJECTIVES ............................................................................................................................... 5 METHODS .................................................................................................................................... 6 RESULTS ...................................................................................................................................... 7 DISTRIBUTION AND STATUS 1999 – 2001 ..................................................................................... 7 DISTRIBUTION 2002 - PRESENT..................................................................................................... 7 CONTROL