U.S. EPA, Pesticides, Label, LAMBDA-CYHALOTHRIN 250 CS
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Restricted Use Product Summary Report
Page 1 of 17 Restricted Use Product Summary Report (January 19, 2016) Percent Active Registration # Name Company # Company Name Active Ingredient(s) Ingredient 4‐152 BONIDE ORCHARD MOUSE BAIT 4 BONIDE PRODUCTS, INC. 2 Zinc phosphide (Zn3P2) 70‐223 RIGO EXOTHERM TERMIL 70 VALUE GARDENS SUPPLY, LLC 20 Chlorothalonil 100‐497 AATREX 4L HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 42.6 Atrazine 100‐585 AATREX NINE‐O HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 88.2 Atrazine 100‐669 CURACRON 8E INSECTICIDE‐MITICIDE 100 SYNGENTA CROP PROTECTION, LLC 73 Profenofos 100‐817 BICEP II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 33; 26.1 Atrazine; S‐Metolachlor 100‐827 BICEP LITE II MAGNUM HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 28.1; 35.8 Atrazine; S‐Metolachlor 100‐886 BICEP MAGNUM 100 SYNGENTA CROP PROTECTION, LLC 33.7; 26.1 Atrazine; S‐Metolachlor 100‐898 AGRI‐MEK 0.15 EC MITICIDE/INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2 Abamectin 100‐903 DENIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 2.15 Emamectin benzoate 100‐904 PROCLAIM INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 5 Emamectin benzoate 100‐998 KARATE 1EC 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1075 FORCE 3G INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 3 Tefluthrin Acetochlor; Carbamothioic acid, dipropyl‐ 100‐1083 DOUBLEPLAY SELECTIVE HERBICIDE 100 SYNGENTA CROP PROTECTION, LLC 16.9; 67.8 , S‐ethyl ester 100‐1086 KARATE EC‐W INSECTICIDE 100 SYNGENTA CROP PROTECTION, LLC 13.1 lambda‐Cyhalothrin 100‐1088 SCIMITAR GC INSECTICIDE 100 SYNGENTA CROP PROTECTION, -
Chem7988.Pdf
This article was originally published in a journal published by Elsevier, and the attached copy is provided by Elsevier for the author’s benefit and for the benefit of the author’s institution, for non-commercial research and educational use including without limitation use in instruction at your institution, sending it to specific colleagues that you know, and providing a copy to your institution’s administrator. All other uses, reproduction and distribution, including without limitation commercial reprints, selling or licensing copies or access, or posting on open internet sites, your personal or institution’s website or repository, are prohibited. For exceptions, permission may be sought for such use through Elsevier’s permissions site at: http://www.elsevier.com/locate/permissionusematerial Chemosphere 67 (2007) 2184–2191 www.elsevier.com/locate/chemosphere Assessment of pesticide contamination in three Mississippi Delta oxbow lakes using Hyalella azteca M.T. Moore *, R.E. Lizotte Jr., S.S. Knight, S. Smith Jr., C.M. Cooper USDA-ARS National Sedimentation Laboratory, P.O. Box 1157, Oxford, MS 38655, United States Received 8 September 2006; received in revised form 27 November 2006; accepted 8 December 2006 Available online 26 January 2007 Abstract Three oxbow lakes in northwestern Mississippi, USA, an area of intensive agriculture, were assessed for biological impairment from historic and current-use pesticide contamination using the amphipod, Hyalella azteca. Surface water and sediment samples from three sites in each lake were collected from Deep Hollow, Beasley, and Thighman Lakes from September 2000 to February 2001. Samples were analyzed for 17 historic and current-use pesticides and selected metabolites. -
Historical Perspectives on Apple Production: Fruit Tree Pest Management, Regulation and New Insecticidal Chemistries
Historical Perspectives on Apple Production: Fruit Tree Pest Management, Regulation and New Insecticidal Chemistries. Peter Jentsch Extension Associate Department of Entomology Cornell University's Hudson Valley Lab 3357 Rt. 9W; PO box 727 Highland, NY 12528 email: [email protected] Phone 845-691-7151 Mobile: 845-417-7465 http://www.nysaes.cornell.edu/ent/faculty/jentsch/ 2 Historical Perspectives on Fruit Production: Fruit Tree Pest Management, Regulation and New Chemistries. by Peter Jentsch I. Historical Use of Pesticides in Apple Production Overview of Apple Production and Pest Management Prior to 1940 Synthetic Pesticide Development and Use II. Influences Changing the Pest Management Profile in Apple Production Chemical Residues in Early Insect Management Historical Chemical Regulation Recent Regulation Developments Changing Pest Management Food Quality Protection Act of 1996 The Science Behind The Methodology Pesticide Revisions – Requirements For New Registrations III. Resistance of Insect Pests to Insecticides Resistance Pest Management Strategies IV. Reduced Risk Chemistries: New Modes of Action and the Insecticide Treadmill Fermentation Microbial Products Bt’s, Abamectins, Spinosads Juvenile Hormone Analogs Formamidines, Juvenile Hormone Analogs And Mimics Insect Growth Regulators Azadirachtin, Thiadiazine Neonicotinyls Major Reduced Risk Materials: Carboxamides, Carboxylic Acid Esters, Granulosis Viruses, Diphenyloxazolines, Insecticidal Soaps, Benzoyl Urea Growth Regulators, Tetronic Acids, Oxadiazenes , Particle Films, Phenoxypyrazoles, Pyridazinones, Spinosads, Tetrazines , Organotins, Quinolines. 3 I Historical Use of Pesticides in Apple Production Overview of Apple Production and Pest Management Prior to 1940 The apple has a rather ominous origin. Its inception is framed in the biblical text regarding the genesis of mankind. The backdrop appears to be the turbulent setting of what many scholars believe to be present day Iraq. -
INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES
US Environmental Protection Agency Office of Pesticide Programs INDEX to PESTICIDE TYPES and FAMILIES and PART 180 TOLERANCE INFORMATION of PESTICIDE CHEMICALS in FOOD and FEED COMMODITIES Note: Pesticide tolerance information is updated in the Code of Federal Regulations on a weekly basis. EPA plans to update these indexes biannually. These indexes are current as of the date indicated in the pdf file. For the latest information on pesticide tolerances, please check the electronic Code of Federal Regulations (eCFR) at http://www.access.gpo.gov/nara/cfr/waisidx_07/40cfrv23_07.html 1 40 CFR Type Family Common name CAS Number PC code 180.163 Acaricide bridged diphenyl Dicofol (1,1-Bis(chlorophenyl)-2,2,2-trichloroethanol) 115-32-2 10501 180.198 Acaricide phosphonate Trichlorfon 52-68-6 57901 180.259 Acaricide sulfite ester Propargite 2312-35-8 97601 180.446 Acaricide tetrazine Clofentezine 74115-24-5 125501 180.448 Acaricide thiazolidine Hexythiazox 78587-05-0 128849 180.517 Acaricide phenylpyrazole Fipronil 120068-37-3 129121 180.566 Acaricide pyrazole Fenpyroximate 134098-61-6 129131 180.572 Acaricide carbazate Bifenazate 149877-41-8 586 180.593 Acaricide unclassified Etoxazole 153233-91-1 107091 180.599 Acaricide unclassified Acequinocyl 57960-19-7 6329 180.341 Acaricide, fungicide dinitrophenol Dinocap (2, 4-Dinitro-6-octylphenyl crotonate and 2,6-dinitro-4- 39300-45-3 36001 octylphenyl crotonate} 180.111 Acaricide, insecticide organophosphorus Malathion 121-75-5 57701 180.182 Acaricide, insecticide cyclodiene Endosulfan 115-29-7 79401 -
Genetically Modified Baculoviruses for Pest
INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS This page intentionally left blank INSECT CONTROL BIOLOGICAL AND SYNTHETIC AGENTS EDITED BY LAWRENCE I. GILBERT SARJEET S. GILL Amsterdam • Boston • Heidelberg • London • New York • Oxford Paris • San Diego • San Francisco • Singapore • Sydney • Tokyo Academic Press is an imprint of Elsevier Academic Press, 32 Jamestown Road, London, NW1 7BU, UK 30 Corporate Drive, Suite 400, Burlington, MA 01803, USA 525 B Street, Suite 1800, San Diego, CA 92101-4495, USA ª 2010 Elsevier B.V. All rights reserved The chapters first appeared in Comprehensive Molecular Insect Science, edited by Lawrence I. Gilbert, Kostas Iatrou, and Sarjeet S. Gill (Elsevier, B.V. 2005). All rights reserved. No part of this publication may be reproduced or transmitted in any form or by any means, electronic or mechanical, including photocopy, recording, or any information storage and retrieval system, without permission in writing from the publishers. Permissions may be sought directly from Elsevier’s Rights Department in Oxford, UK: phone (þ44) 1865 843830, fax (þ44) 1865 853333, e-mail [email protected]. Requests may also be completed on-line via the homepage (http://www.elsevier.com/locate/permissions). Library of Congress Cataloging-in-Publication Data Insect control : biological and synthetic agents / editors-in-chief: Lawrence I. Gilbert, Sarjeet S. Gill. – 1st ed. p. cm. Includes bibliographical references and index. ISBN 978-0-12-381449-4 (alk. paper) 1. Insect pests–Control. 2. Insecticides. I. Gilbert, Lawrence I. (Lawrence Irwin), 1929- II. Gill, Sarjeet S. SB931.I42 2010 632’.7–dc22 2010010547 A catalogue record for this book is available from the British Library ISBN 978-0-12-381449-4 Cover Images: (Top Left) Important pest insect targeted by neonicotinoid insecticides: Sweet-potato whitefly, Bemisia tabaci; (Top Right) Control (bottom) and tebufenozide intoxicated by ingestion (top) larvae of the white tussock moth, from Chapter 4; (Bottom) Mode of action of Cry1A toxins, from Addendum A7. -
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. -
U.S. EPA, Pesticides, Label, TEFLUTHRIN TECHNICAL, 7/19
\09-lo\S- 0)-1'1-2, J}!) UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 OFFICE OF PREVENTION, PESTICIDES AND TOXIC SUBSTANCES July 19,2010 Pat Dinnen Syngenta Crop Protection, Inc. P.O. Box 18300 Greensboro, NC 27419 Subject: Label Notification(s) for Pesticide Registration Notice 2007-4 Amending the Storage and Disposal Language Dear Pat Dinnen: The Agency is in receipt of your Application(s) for Pesticide Notification under Pesticide Registration Notice PRN 2007-4 dated June 22,2010 for the following product(s): Fenoxycarb Technical EPA Reg. No.1 00-723 Cypermethrin Technical EPA Reg. No. 100-989 Tefluthrin Technical EPA Reg. No. 100-1015 Lambda-Cyhalothrin Manufacturing CS EPA Reg. No. 100-1107 Lufenuron Techincal EPA Reg. No. 100-1175 Lambda-Cyhalothrin 250 CS MUP EPA Reg. No. 100-1251 Cypermethrin 250EC MUP EPA Reg. No. 100-1301 The Registration Division (RD) has conducted a review of this request for applicability under PRN 2007-4 and finds that the label change(s) requested falls within the scope of PRN-98-10. The label has been date-stamped "Notification" and will be placed in our records. Please be reminded that 40 CFR Part 156. 140(a)(4) requires that a batch code, lot niImber, or other code identifying the batch of the pesticide distributed and sold be placed on nomefillable containers. The code may appear either on the label (and can be added by non-notificationlPR Notice 98-10) or durably marked on the container itself. If you have any questions, please contact Regina Foushee'-Smith at 703-605-0780. -
(12) United States Patent (10) Patent No.: US 8,852,618 B2 Clough (45) Date of Patent: Oct
USOO8852618B2 (12) United States Patent (10) Patent No.: US 8,852,618 B2 Clough (45) Date of Patent: Oct. 7, 2014 (54) INSECTICIDAL MIXTURE CONTAINING CA 2429218 A1 6, 2002 GAMMA-CYHALOTHRN CH 689326 A5 4f1995 EP O237227 A1 9, 1987 EP 0771526 A2 5, 1997 (75) Inventor: Martin Stephen Clough, Bracknell EP O988788 A1 3f2000 (GB) FR 272O230 A1 12/1995 JP 63. 126805 A2 5, 1988 (73) Assignee: Syngenta Limited, Guildford (GB) JP 63126805 A2 5, 1988 JP 63126805 5, 1998 c - r WO WO 86 O7525 A1 12, 1986 (*) Notice: Subject to any disclaimer, the term of this WO WO 93 03618 A2 3, 1993 patent is extended or adjusted under 35 WO WO95 229O2 A1 8/1995 U.S.C. 154(b) by 824 days. WO WO9533380 A1 12, 1995 WO WO 96 16543 A2 6, 1996 (21) Appl. No.: 12/633,063 WO WO97 06687 A1 2/1997 WO WO974O692 A1 11, 1997 (22) Filed: Dec.a V88, 2009 WO WOOOO2453 A1 1, 2000 OTHER PUBLICATIONS (65) Prior Publication Data US 201O/OO81714 A1 Apr. 1, 2010 Canadian Office Action (Applin. No. 2,452,515 filed: Jul. 10, 2002) mailing date Oct. 1, 2010 (pp. 1-2). Related U.S. Application Data Allen et al. Transgenic & Conventional Insect & Weed Control Sys tems; Proceedings of the Beltwide Cotton Conference, vol. 2, 1065 (62) Division of application No. 10/484.745, filed as 1068 (1999), USA. application No. PCT/GB02/03181 on Jul. 10, 2002, Anonymous; Pesticide Mixtures for Control of Insect and Acarid now Pat. No. -
Ants in the Home Fact Sheet No
Ants in the Home Fact Sheet No. 5.518 Insect Series|Home and Garden by W.S. Cranshaw* Almost anywhere in the state one the nest, tend the young and do other Quick Facts travels, ants will be the most common necessary colony duties. Many kinds of insects that can be found in yards, gardens, ants produce workers that are all the • Most ants that are found in fields and forests. Tremendous numbers same size (monomorphic); some, such as homes nest outdoors and of ants normally reside in a typical house field ants, have workers that vary in size enter homes only to search lot, although most lead unobserved lives (polymorphic). for food or water. underground or otherwise out of sight. Each colony contains one or, sometimes, Often it is only when they occur indoors or a few queens (Figure 1). These are fertile • Almost all ants are workers, produce their periodic mating swarms that females that are larger than workers and wingless females that search they come to human attention. dedicated to egg production. The minute for food and maintain the Overall, the activities of ants are quite eggs are taken from the queen and tended colony. beneficial. Many feed on other insects, by the workers. Upon egg hatch, the • A small proportion of an including pest insects. Ant scavenging pale-colored, legless larvae are fed and helps to recycle organic matter and their protected by the workers. When full-grown, ant colony are winged tunneling is useful in aerating and mixing ant larvae produce a smooth silken cocoon reproductive forms. -
The Fall Armyworm – a Pest of Pasture and Hay
The Fall Armyworm – A Pest of Pasture and Hay. Allen Knutson Extension Entomologist, Texas A&M AgriLife Extension Texas A&M AgriLife Research and Extension Center, Dallas, 2019 revision The fall armyworm, Spodoptera frugiperda, is a common pest of bermudagrass, sorghum, corn, wheat and rye grass and many other crops in north and central Texas. Larvae of fall armyworms are green, brown or black with white to yellowish lines running from head to tail. A distinct white line between the eyes forms an inverted “Y” pattern on the face. Four black spots aligned in a square on the top of the segment near the back end of the caterpillar are also characteristic. Armyworms are very small (less than 1/8 inch) at first, cause little plant damage and as a result often go unnoticed. Larvae feed for 2-3 weeks and full grown larvae are about 1 to 1 1/2 inches long. Given their immense appetite, great numbers, and marching ability, fall armyworms can damage entire fields or pastures in a few days. Once the armyworm larva completes feeding, it tunnels into the soil to a depth of about an inch and enters the pupal stage. The armyworm moth emerges from the pupa in about ten days and repeats the life cycle. The fall armyworm moth has a wingspan of about 1 1/2 inches. The front pair of wings is dark gray with an irregular pattern of light and dark areas. Moths are active at night when they feed on nectar and deposit egg masses. A single female can deposit up to 2000 eggs and there are four to five generations per year. -
Agricultural Chemical Usage Restricted Use Summary Agricultural Statistics Board October 2000 1 NASS, USDA Highlights
United States Department of Agriculture Agricultural Chemical National Agricultural Statistics Usage Service 1999 Restricted Use Summary Ag Ch 1 (00) a October 2000 Update Alert The herbicide trifluralin was erroneously listed in the corn, upland cotton, peanuts, fall potatoes, soybeans and sunflower tables (pages 3-7). Trifluralin is not restricted for use on those crops. In addition, summary errors for the chemicals ethyl parathion and methyl parathion were discovered for sunflowers in Kansas. Previously published applications of the insecticide ethyl parathion on sunflowers in Kansas were in error and should have all been reported as applications of methyl parathion. The affected sunflower table has been revised (page 7). 1999 Agricultural Chemical Use Estimates for Restricted Use Pesticides Overview: As determined by the U.S. Environmental Protection Agency (EPA), a restricted use pesticide is a pesticide which is available for purchase and use only by certified pesticide applicators or persons under their direct supervision and only for the uses covered by the certified applicator’s certification. This group of pesticides is not available for use by the general public because of the very high toxicities and /or environmental hazards associated with these active ingredients. An active ingredient may be restricted for one crop but not for another. This report shows only those active ingredients which are restricted for each specific crop, based on the “Restricted Use Product (RUP) Report, June 2000" published by the EPA. The agricultural chemical use estimates in this report are based on data compiled from the Agricultural Resource Management Study, the Fruit Chemical Use Survey, and the 1999 Fall Area Survey. -
AP-42, CH 9.2.2: Pesticide Application
9.2.2PesticideApplication 9.2.2.1General1-2 Pesticidesaresubstancesormixturesusedtocontrolplantandanimallifeforthepurposesof increasingandimprovingagriculturalproduction,protectingpublichealthfrompest-bornediseaseand discomfort,reducingpropertydamagecausedbypests,andimprovingtheaestheticqualityofoutdoor orindoorsurroundings.Pesticidesareusedwidelyinagriculture,byhomeowners,byindustry,andby governmentagencies.Thelargestusageofchemicalswithpesticidalactivity,byweightof"active ingredient"(AI),isinagriculture.Agriculturalpesticidesareusedforcost-effectivecontrolofweeds, insects,mites,fungi,nematodes,andotherthreatstotheyield,quality,orsafetyoffood.Theannual U.S.usageofpesticideAIs(i.e.,insecticides,herbicides,andfungicides)isover800millionpounds. AiremissionsfrompesticideusearisebecauseofthevolatilenatureofmanyAIs,solvents, andotheradditivesusedinformulations,andofthedustynatureofsomeformulations.Mostmodern pesticidesareorganiccompounds.EmissionscanresultdirectlyduringapplicationorastheAIor solventvolatilizesovertimefromsoilandvegetation.Thisdiscussionwillfocusonemissionfactors forvolatilization.Thereareinsufficientdataavailableonparticulateemissionstopermitemission factordevelopment. 9.2.2.2ProcessDescription3-6 ApplicationMethods- Pesticideapplicationmethodsvaryaccordingtothetargetpestandtothecroporothervalue tobeprotected.Insomecases,thepesticideisapplieddirectlytothepest,andinotherstothehost plant.Instillothers,itisusedonthesoilorinanenclosedairspace.Pesticidemanufacturershave developedvariousformulationsofAIstomeetboththepestcontrolneedsandthepreferred