Insecticides and Repellents Used for Mosquito Control with Emphasis On
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Evaluation of Fluralaner and Afoxolaner Treatments to Control Flea
Dryden et al. Parasites & Vectors (2016) 9:365 DOI 10.1186/s13071-016-1654-7 RESEARCH Open Access Evaluation of fluralaner and afoxolaner treatments to control flea populations, reduce pruritus and minimize dermatologic lesions in naturally infested dogs in private residences in west central Florida USA Michael W. Dryden1*, Michael S. Canfield2, Kimberly Kalosy1, Amber Smith1, Lisa Crevoiserat1, Jennifer C. McGrady1, Kaitlin M. Foley1, Kathryn Green2, Chantelle Tebaldi2, Vicki Smith1, Tashina Bennett1, Kathleen Heaney3, Lisa Math3, Christine Royal3 and Fangshi Sun3 Abstract Background: A study was conducted to evaluate and compare the effectiveness of two different oral flea and tick products to control flea infestations, reduce pruritus and minimize dermatologic lesions over a 12 week period on naturally infested dogs in west central FL USA. Methods: Thirty-four dogs with natural flea infestations living in 17 homes were treated once with a fluralaner chew on study day 0. Another 27 dogs living in 17 different homes were treated orally with an afoxolaner chewable on day 0, once between days 28–30 and once again between days 54–60. All products were administered according to label directions by study investigators. Flea populations on pets were assessed using visual area counts and premise flea infestations were assessed using intermittent-light flea traps on days 0, 7, 14, 21, and once between days 28–30, 40–45, 54–60 and 82–86. Dermatologic assessments were conducted on day 0 and once monthly. Pruritus assessments were conducted by owners throughout the study. No concurrent treatments for existing skin disease (antibiotics, anti-inflammatories, anti-fungals) were allowed. -
4. Chemical and Physical Information
PYRETHRINS AND PYRETHROIDS 131 4. CHEMICAL AND PHYSICAL INFORMATION 4.1 CHEMICAL IDENTITY The naturally-occurring pyrethrins, extracted from chrysanthemum flowers, are esters of chrysanthemic acid (Pyrethrin I, Cinerin I, and Jasmolin I) and esters of pyrethric acid (Pyrethrin II, Cinerin II, and Jasmolin II). In the United States, the pyrethrum extract is standardized as 45–55% w/w total pyrethrins. The typical proportion of Pyrethrins I to II is 0.2:2.8, while the ratio of pyrethrins:cinerins:jasmolins is 71:21:7 (Tomlin 1997). Information regarding the chemical identity of the pyrethrins is presented in Table 4-1. Pyrethroids are synthetic esters derived from the naturally-occurring pyrethrins. One exception to the axiom that all pyrethroids are esters of carboxylic acids is noteworthy. There is a group of oxime ethers that exhibits insecticidal activity similar in nature to the pyrethrins and pyrethroid esters (Davies 1985). Little data exist regarding these compounds, and no commercial products have been produced. Commercially available pyrethroids include allethrin, bifenthrin, bioresmethrin, cyfluthrin, cyhalothrin, cypermethrin, deltamethrin, esfenvalerate (fenvalerate), flucythrinate, flumethrin, fluvalinate, fenpropathrin, permethrin, phenothrin, resmethrin, tefluthrin, tetramethrin, and tralomethrin. Information regarding the chemical identity of pyrethroids is shown in Table 4-2. With the exception of deltamethrin, pyrethroids are a complex mixture of isomers rather than one single pure compound. For pyrethroids possessing the cyclopropane moiety, isomerism about the cyclopropane ring greatly influences the toxicity of these insecticides. The presence of two chiral centers in the ring results in two pairs of diastereomers. The diastereomers and their nonsuperimposable mirror images (enantiomers) are illustrated in Figure 4-1. -
MP144: Ornamental Insect Control for Homeowners
ORNAMENTAL INSECT CONTROL FOR HOMEOWNERS OUTDOOR ORNAMENTAL INSECT CONTROL Amount Formulation Pest Insecticide and Formulation* Per Gallon Spray Remarks and Precautions Aphid acephate Follow label directions. acetamiprid Follow label directions. beta-cyfluthrin 0.0015% + imidacloprid 0.012% ready to use Follow label directions. (Bayer Advanced Dual Action Rose & Flower Insect Killer Ready-To-Use) bifenthrin Follow label directions. cyfluthrin Follow label directions. dinotefuran (Ortho Tree & Shrub Insect Control Plus Per label directions. Miracle-Gro Plant Food Concentrate 0.43%, Ortho Tree & Shrub Insect Control Granules 2.0%) horticultural oils 1%-2% Follow label directions. imidacloprid (Bayer Advanced) Follow label directions. insecticidal soap 1%-2% Thorough coverage is necessary. Spray must contact pests to be effective. Repeat spray three times at 5- to 7-day intervals. malathion (various) Follow label directions. pyrethrin/pyrethrum Follow label directions. pyrethroids (various) ready to use and concentrate Follow label directions. Azalea Leaf Miner acephate (Orthene TTO) 1 tsp Per label directions. beta-cyfluthrin 0.0015% + imidacloprid 0.012% ready to use Follow label directions. (Bayer Advanced Dual Action Rose & Flower Insect Killer Ready-To-Use) dinotefuran (Ortho Tree & Shrub Insect Control Plus Per label directions. Miracle-Gro Plant Food Concentrate 0.43%, Ortho Tree & Shrub Insect Control Granules 2.0%) imidacloprid (Bayer Advanced) Bagworm Bacillus thuringiensis 2 tsp Per label directions. (Biotrol WP, Thuricide, Sok-Bt) beta-cyfluthrin 0.0015% + imidacloprid 0.012% ready to use Follow label directions. (Bayer Advanced Dual Action Rose & Flower Insect Killer Ready-To-Use) malathion (various) Per label directions. In winter, hand-pick and burn if only a few bagworms are present. -
Scanned Document
cc: Eric Bohnenblust Alexandra Dunn Cheryl Dunton Michael Goodis Arnold Layne Anna Lowit Autumn Metzger Jennifer Saunders OPP Docket FIFRA Scientific Advisory Panel: Robert E. Chapin, PhD Joseph Shaw, PhD Sonya K. Sobrian, PhD Clifford P. Weisel, PhD Raymond S.H. Yang, PhD FQPA Science Review Board Members: Arthur Appel, PhD Michael J. Daniels, ScD Marion Ehrich, PhD Jerome Hogsette, PhD Eric Kwok, PhD Lisa Murphy, VMD Weste Osbrink, PhD Michael K. Rust, PhD Jeffrey G Scott, PhD Keith Shockley, PhD Daniel E. Snyder, DVM, PhD Larisa Vredevoe, PhD 2 FIFRA Scientific Advisory Panel Meeting Minutes and Final Report No. 2019-02 Peer Review on EPA Office of Pesticide Programs’ Proposed Guidelines for Efficacy Testing of Topically Applied Pesticides Used Against Certain Ectoparasitic Pests on Pets June 11-14, 2019 FIFRA Scientific Advisory Panel Meeting Held at U.S. Environmental Protection Agency Conference Center Lobby Level One Potomac Yard (South Bldg.) 2777 S. Crystal Drive, Arlington, VA 22202 3 Page Blank 4 NOTICE The Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA) Scientific Advisory Panel (SAP) is a federal advisory committee operating in accordance with the Federal Advisory Committee Act and established under the provisions of FIFRA as amended by the Food Quality Protection Act (FQPA) of 1996. The FIFRA SAP provides advice, information, and recommendations to the U.S. Environmental Protection Agency (EPA or Agency) Administrator on pesticides and pesticide-related issues regarding the impact of regulatory actions on health and the environment. The SAP serves as a primary scientific peer review mechanism of the EPA, Office of Pesticide Programs (OPP), and is structured to provide balanced expert assessment of pesticide and pesticide-related matters facing the Agency. -
Safety of Pyrethrin and Pyrethroid Pesticides Used to Control Adult Mosquitoes
SAFETY OF PYRETHRIN AND PYRETHROID PESTICIDES USED TO CONTROL ADULT MOSQUITOES Questions and Answers for Public Health Professionals Division of Environmental and Occupational Disease Control Division of Communicable Disease Control California Department of Public Health 1. What is the primary method used to control West Nile virus? Mosquito control is the most effective means of reducing the risk of people becoming infected with West Nile virus (WNV). Mosquito control targets both the aquatic, immature stages of the mosquito and the adult stage (CDHS, 2005a). Larval control Control of larval mosquitoes is the backbone of most mosquito control programs in California. Pesticides added to the water to kill mosquito larvae are called larvicides. These products may be applied by hand, with a power backpack, from all-terrain vehicles (ATVs) or trucks, and in very large or inaccessible areas with helicopters and airplanes. Pesticides used for larviciding include bacterial products (Bacillus thuringiensis var. israelensis (Bti) and B. sphaericus (Bs), surface agents (highly refined mineral oils or monomolecular films that spread across the surface of the water), and the insect growth regulators methoprene and dimilin (chemicals that are added to the water to disrupt the normal maturation process of mosquito larvae). For more information on larvicidal agents, please refer to the fact sheet titled "Pesticides and Mosquito Control" (US EPA, 2002). Adult mosquito control Adult mosquito control is a means to rapidly knockdown biting adult mosquitoes. This can become necessary when larval control measures are insufficient or not feasible. Adulticiding may be initiated when there is evidence of significant WNV transmission in a region. -
Pyrethrum Secondary Metabolism: Biosynthesis, Localization and Ecology of Defence Compounds
Pyrethrum Secondary Metabolism: Biosynthesis, Localization and Ecology of Defence Compounds Aldana Ramirez Thesis committee Promotors Prof. dr.ir. H.J. Bouwmeester Professor of Plant Physiology Wageningen University Prof. dr. M. Dicke Professor of Entomology Wageningen University Thesis co-supervisor Dr.ir. M. A. Jongsma Senior scientist, Plant Research International Wageningen University and Research Center Other members Prof.dr.ir. N.P.R. Anten, Wageningen University Prof. A. Tissier, Leibniz Institute of Plant Biochemistry, Halle, Germany Dr. K. Posthuma, Enza Zaden, Research & Development B.V., Enkhuizen Dr. M.C.R. Franssen, Wageningen University This research was conducted under the auspices of the Graduate School of Experimental Plant Sciences Pyrethrum Secondary Metabolism: Biosynthesis, Localization and Ecology of Defence Compounds Aldana Ramirez Thesis submittted in fulfillment of the requirements for the degree of doctor at Wageningen University by the authority of the Rector Magnificus Prof. dr. M.J. Kropff, in the presence of the Thesis Committee appointed by the Academic Board to be defended in public on Friday 3 May 2013 at 1.30 p.m. in the Aula. Aldana Ramirez Pyrethrum Secondary Metabolism: Biosynthesis, Localization and Ecology of Defence Compounds, 190 pages Thesis, Wageningen University, Wageningen, NL (2013) With references, with summaries in Dutch and English ISBN 978-94-6173-517-1 “Consistency is the last refuge of the unimaginative” Oscar Wilde Contents Chapter 1 General introduction. 9 Chapter 2 Bidirectional secretions from glandular trichomes 27 of pyrethrum enable immunization of seedlings. Chapter 3 A single cytochrome P450 enzyme catalyses the 63 formation of chrysanthemic acid from chrysanthemol in pyrethrin biosynthesis. Chapter 4 Cloning and characterization of a trichome-specific 101 13-lipoxygenase expressed during pyrethrin biosynthesis in pyrethrum (Tanacetum cinerariifolium). -
Pyrethrins and Pyrethroids
Pyrethrins CHAPTER 4 HIGHLIGHTS Strongly lipophilic Crude pyrethrum is a dermal Pyrethrins and Pyrethroids & respiratory allergen Easily absorbed by GI tract & pulmonary membranes Relatively low mammalian PYRETHRINS toxicity Pyrethrum is the oleoresin extract of dried chrysanthemum flowers. The extract contains about 50% active insecticidal ingredients known as pyrethrins. The ketoalco- holic esters of chrysanthemic and pyrethroic acids are known as pyrethrins, cinerins SIGNS & SYMPTOMS and jasmolins. These strongly lipophilic esters rapidly penetrate many insects and paralyze their nervous systems. Both crude pyrethrum extract and purified pyrethrins Contact dermatitis are contained in various commercial products, commonly dissolved in petroleum Rhinitis, asthma distillates. Some are packaged in pressurized containers (“bug bombs”), usually in combination with the synergists piperonyl butoxide and n-octyl bicycloheptene dicar- boximide. The synergists retard enzymatic degradation of pyrethrins. Pyrethrum and pyrethrin products are used mainly for indoor pest control. They are not sufficiently TREATMENT stable in light and heat to remain as active residues on crops. The synthetic insecticides Antihistamines known as pyrethroids (chemically similar to pyrethrins) have the stability needed for agricultural applications. Pyrethroids are discussed separately below. Epinephrine for anaphylaxis as required Topical corticosteroid for Toxicology contact dermatitis Crude pyrethrum is a dermal and respiratory allergen, probably due mainly to non- Flush eyes as necessary insecticidal ingredients. Contact dermatitis and allergic respiratory reactions (rhinitis and asthma) have occurred following exposures.1,2 Single cases exhibiting anaphy- Consider gastric emptying or lactic3 and pneumonitic manifestations4 have also been reported. Pulmonary symp- charcoal adsorption toms may be due to inhalation of the hydrocarbon vehicle(s) of the insecticides. -
United States Patent (19) 11 3,941,829 Pissiotas Et Al
United States Patent (19) 11 3,941,829 Pissiotas et al. (45) Mar. 2, 1976 54 N-PHENYL-N'-CARBOPHENOXY FORMAMIDINES 57 ABSTRACT (75) Inventors: Georg Pissiotas, Lorrach, Germany; Phenylformamidines of the formula Dieter Dürr, Bottmingen, Switzerland 4 R3 (73) Assignee: Ciba-Geigy Corporation, Ardsley, R N.Y. R5 NiccH-N / (22 Filed: Dec. 1, 1972 N (21) Appl. No.: 311,058 COOR2 R6 R7 30 Foreign Application Priority Data Dec. 7, 1971 Switzerland....................... 17790/7 wherein R represents hydrogen, alkyl, alkenyl or al Dec. 7, 1971 Switzerland....................... 1779/7 kynyl, R represents a-naphthyl, Jan. 26, 1972 Switzerland......................... 1224/72 Oct. 27, 1972 Switzerland....................... 5729/72 52) U.S. Cl...... 260f471 C; 260/240 G; 260/465 D; 260/470; 260/472; 424/277; 424/278; 424/285; 424/300 (51) int. Cl......................................... C07C 125/06 (58) Field of Search..... 260/471 C, 472, 470, 240 G 56 References Cited or substituted phenyl, FOREIGN PATENTS OR APPLICATIONS wherein the phenyl group is not substituted simulta 890,922 lf 972 Canada neously in the 2-position by a methyl group and in the 2,202,034 | 972 Germany 4-position by a chlorine atom, R. R. R. R. and R. 2,123,001 81972 France represent one or more radicals which are the same or 778,383 7/1972 Belgium different, such as hydrogen or halogen atoms or alkyl, alkoxy, alkylthio, alkenyloxy, alkynyloxy, alkoxycar Primary Examiner-Anton H. Sutto bonyl, CFs, cyano or nitro groups, their process for Assistant Examiner-Michael Shippen the manufacture and their use in pest control. -
A Quick Reference Guide to Pesticides for Pest Management Professionals Working in and Around Structures 2020
W 658 A Quick Reference Guide to Pesticides for Pest Management Professionals Working in and Around Structures 2020 A Quick Reference Guide to Pesticides for Pest Management Professionals Working in and Around Structures Karen Vail, Professor, and Jennifer Chandler, Research Specialist III, Entomology and Plant Pathology This publication provides a quick reference to pesticides and methods for the pest management professional to use in solving pest management problems in and around structures. A thorough description of pest identification including images, inspection and detection techniques, exclusion, sanitation, other environmental modifications, and pesticide formulations can be found in the following UT Extension publications (https://ag.tennessee.edu/PSEP/Forms/F818.pdf): Vail, K.M., G. Burgess, R. Gerhardt and C. Harper [eds.]. 2007. PB 1673 General Pest and Rodent Control Pesticide Applicator Licensing Manual (GRC). pp. 130. Vail, K., G. Burgess, R. Gerhardt and C. Jones [eds.]. 2002. PB 1685 Public Health Mosquito Control: The Tennessee Mosquito Control Handbook (Pesticide Applicator Licensing Manual). pp. 54. Vail, K., D. Hensley, G. Burgess, C. Pless and A. Taylor [eds.]. 2014. PB 1703 Wood-Destroying Organisms Licensing Manual. pp. 76. Vail, K.M., E. Burgess, R. Gerhardt, and Craig Harper. 2006. PB 1732 Industrial, Institutional, Structural and Health Related Pest Management Certification Manual (Category 7). pp. 105. Vail, K.M., E.E. Burgess, R. Gerhardt, C. Jones, J. Skinner and C. Harper. 2003. PB 1733. Public Health Pest Control (Category 8). pp. 99. Further references for household pest identification: Manuals: Bennett, G.W., J.M. Owens, & R.M. Corrigan. 2011. Scientific Guide to Pest Management Operations, seventh edition Cleveland, OH: Questex Publishing. -
Reregistration Eligibility Decision (RED) for Pyrethrins
United States Prevention, Pesticides EPA 738-R-06-004 Environmental Protection And Toxic Substances June 2006 Agency (7508C) _________________________________________________________________ Reregistration Eligibility Decision for Pyrethrins List B Case No. 2580 Reregistration Eligibility Decision (RED) Document for Pyrethrins Approved by: /S/ . Debra Edwards, Ph. D. Director Special Review and Reregistration Division Date: June 7, 2006 . Page 2 of 108 TABLE OF CONTENTS Executive Summary ....................................................................................................................... 7 I. Introduction......................................................................................................................... 11 II. Chemical Overview........................................................................................................... 12 A. Regulatory History...................................................................................................... 12 B. Chemical Identification .............................................................................................. 13 C. Use Profile.................................................................................................................... 16 1. Pyrethrins Use Profile................................................................................................. 16 III. Summary of Pyrethrins Risk Assessments ............................................................... 17 A. Human Health Risk Assessment............................................................................... -
57518 Federal Register / Vol. 61, No. 216 / Wednesday, November 6, 1996 / Rules and Regulations
57518 Federal Register / Vol. 61, No. 216 / Wednesday, November 6, 1996 / Rules and Regulations ENVIRONMENTAL PROTECTION implement certain pollution prevention, (BPT), §§ 455.43 and 455.63 (BCT), and AGENCY recycle and reuse practices. Facilities §§ 455.44 and 455.64 (BAT) are choosing and implementing the established in the National Pollutant 40 CFR Part 455 pollution prevention alternative will Discharge Elimination System (NPDES) receive a discharge allowance. permits. [FRL±5630±9] The final rule will benefit the ADDRESSES: For additional technical RIN 2040±AC21 environment by removing toxic information write to Ms. Shari H. pollutants (pesticide active ingredients Zuskin, Engineering & Analysis Division Pesticide Chemicals Category, and priority pollutants) from water (4303), U.S. EPA, 401 M Street SW, Formulating, Packaging and discharges that have adverse effects on Washington, D.C. 20460 or send e-mail Repackaging Effluent Limitations human health and aquatic life. EPA has to: [email protected] or call Guidelines, Pretreatment Standards, estimated the compliance costs and at (202) 260±7130. For additional and New Source Performance economic impacts expected to result economic information contact Dr. Lynne Standards from the Zero Discharge/Pollution Tudor at the address above or by calling Prevention Alternative (i.e., Zero/P2 AGENCY: Environmental Protection (202) 260±5834. Agency. Alternative). The Agency has determined that the Zero/P2 Alternative The complete record (excluding ACTION: Final rule. will result in a similar removal of toxic confidential business information) for this rulemaking is available for review SUMMARY: This final regulation limits pound equivalents per year at EPA's Water Docket; 401 M Street, the discharge of pollutants into (approximately 7.6 million toxic pound SW, Washington, DC 20460. -
US EPA-Pesticides; Pyrethrins
UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 OFFICE OF PREVENTION, PESTICIDES AND TOXIC SUBSTANCES August 16, 2005 MEMORANDUM SUBJECT: Review of Pyrethrins Incident Reports - Second Revision DP Barcode D320300, Chemical #069001 FROM: Jerome Blondell, Ph.D., Health Statistician Chemistry and Exposure Branch 1 Health Effects Division (7509C) THRU: David J. Miller, Branch Chief Chemistry and Exposure Branch 1 Health Effects Division (7509C) TO: Christine Olinger, Chemist Reregistration Branch 1 Health Effects Division (7509C) BACKGROUND The following data bases have been consulted for the poisoning incident data on the active ingredient Pyrethrins (PC Code:069001): 1) OPP Incident Data System (IDS) - reports of incidents from various sources, including registrants, other federal and state health and environmental agencies and individual consumers, submitted to OPP since 1992. Reports submitted to the Incident Data System represent anecdotal reports or allegations only, unless otherwise stated. Typically no conclusions can be drawn implicating the pesticide as a cause of any of the reported health effects. Nevertheless, sometimes with enough documentation risk mitigation measures may be suggested. 2) Poison Control Centers - as the result of a data purchase by EPA, OPP received Poison Control Center data covering the years 1993 through 1998 for all pesticides. Most of the national Poison Control Centers (PCCs) participate in a national data collection system, the Toxic Exposure Surveillance System which obtains data from about 65-70 centers at hospitals and universities. PCCs provide telephone consultation for individuals and health care providers on suspected poisonings, involving drugs, household products, pesticides, etc. 3) California Department of Pesticide Regulation - California has collected uniform data on suspected pesticide poisonings since 1982.