Pesticide Resistance of Agricultural Pests in Japan
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Global Insecticide Use for Vector-Borne Disease Control
WHO/CDS/NTD/WHOPES/GCDPP/2007.2 GLOBAL INSECTICIDE USE FOR VECTOR-BORNE DISEASE CONTROL M. Zaim & P. Jambulingam DEPARTMENT OF CONTROL OF NEGLECTED TROPICAL DISEASES (NTD) WHO PESTICIDE EVALUATION SCHEME (WHOPES) First edition, 2002 Second edition, 2004 Third edition, 2007 © World Health Organization 2007 All rights reserved. The designations employed and the presentation of the material in this publication do not imply the expression of any opinion whatsoever on the part of the World Health Organization concerning the legal status of any country, territory, city or area or of its authorities, or concerning the delimitation of its frontiers or boundaries. Dotted lines on maps represent approximate border lines for which there may not yet be full agreement. The mention of specific companies or of certain manufacturers’ products does not imply that they are endorsed or recommended by the World Health Organization in preference to others of a similar nature that are not mentioned. Errors and omissions excepted, the names of proprietary products are distinguished by initial capital letters. All reasonable precautions have been taken by the World Health Organization to verify the information contained in this publication. However, the published material is being distributed without warranty of any kind, either express or implied. The responsibility for the interpretation and use of the material lies with the reader. In no event shall the World Health Organization be liable for damages arising from its use. The named authors alone are responsible for the views expressed in this publication. CONTENTS Page Acknowledgements i Introduction 1 Collection of information 2 Data analysis and observations on reporting 3 All uses in vector control 6 Malaria vector control 22 Dengue vector control 38 Chagas disease vector control 48 Leishmaniasis vector control 52 Other vector-borne disease control 56 Selected insecticides – DDT 58 Selected insecticides – Insect growth regulators 60 Selected insecticides – Bacterial larvicides 62 Country examples 64 Annex 1. -
Dimethoate 4EC Systemic Insecticide – Miticide ACTIVE INGREDIENT: PRECAUTIONARY STATEMENTS (Cont.) Dimethoate*
GROUP 1B INSECTICIDE Dimethoate 4EC Systemic Insecticide – Miticide ACTIVE INGREDIENT: PRECAUTIONARY STATEMENTS (Cont.) Dimethoate* .......................................................... 43.5% Mixers, loaders, applicators, flaggers, and other handlers must OTHER INGREDIENTS: .......................................... 56.5% wear: Long-sleeved shirt and long pants, shoes plus socks, goggles TOTAL: .............................................................. 100.0% or face shield, chemical-resistant gloves, a NIOSH-approved * This product contains 4 pounds of dimethoate per gallon. dust/mist filtering respirator with MSHA/NIOSH approval number prefix TC-21C or a NIOSH-approved respirator with any N, R, P, or KEEP OUT OF REACH OF CHILDREN HE filter, and chemical-resistant apron when mixing, loading, clean- ing up spills, or equipment. WARNING See Engineering Controls for additional requirements and excep- Si usted no entiende la etiqueta, busque a alguien para que se la ex- tions. plique a usted en detalle. (If you do not understand the label, find Follow manufacturer’s instructions for cleaning/maintaining PPE. If someone to explain it to you in detail.) no such instructions for washables exist, use detergent and hot water. Keep and wash PPE separately from other laundry. See FIRST AID Below Discard clothing and other absorbent materials that have been EPA Reg. No. 19713-231 Net Content: drenched or heavily contaminated with this product’s concentrate. EPA Est. No. 19713-GA-001 2.5 Gals. (9.46 L) Do not reuse them. ENGINEERING CONTROLS FIRST AID Mixers and loaders supporting aerial application to alfalfa, cotton, IF SWALLOWED: soybeans, corn, safflower, sorghum, and wheat, must use a closed • Call a poison control center or doctor immediately for treatment system that meets the requirements listed in the Worker Protections advice. -
Review of the Mammalian Toxicology
REVIEW OF THE MAMMALIAN TOXICOLOGY AND METABOLISM/TOXICOKINETICS OF FENTHION The APVMA Review of Fenthion © Australian Pesticides and Veterinary Medicines Authority 2012 ISBN 978-0-9873591-5-5 (electronic) This document was originally published in 2005 as part of the preliminary review findings report for Part 1 of the fenthion review. It was subsequently updated in 2007, and revised in 2008. Ownership of intellectual property rights in this publication Unless otherwise noted, copyright (and any other intellectual property rights, if any) in this publication is owned by the Australian Pesticides and Veterinary Medicines Authority (APVMA). Creative Commons licence With the exception of the Coat of Arms, this publication is licensed under a Creative Commons Attribution 3.0 Australia Licence. This is a standard form agreement that allows you to copy, distribute, transmit and adapt this publication provided that you attribute the work. A summary of the licence terms is available from www.creativecommons.org/licenses/by/3.0/au/deed.en. The full licence terms are available from www.creativecommons.org/licenses/by/3.0/au/legalcode. The APVMA’s preference is that you attribute this publication (and any approved material sourced from it) using the following wording: Source: Licensed from the Australian Pesticides and Veterinary Medicines Authority (APVMA) under a Creative Commons Attribution 3.0 Australia Licence. This report was prepared for the APVMA by the Department of Health and Aging Office of Chemical Safety. In referencing this document the Department of Health and Aging Office of Chemical Safety should be cited as the author and the Australian Pesticides and Veterinary Medicines Authority as the publisher and copyright owner. -
Malathion General Fact Sheet
MALATHION GENERAL FACT SHEET What is malathion Malathion is an insecticide in the chemical family known as organophosphates. Products containing malathion are used outdoors to control a wide variety of insects in agricultural settings and around people’s homes. Malathion has also been used in public health mosquito control and fruit fly eradication programs. Malathion may also be found in some special shampoos for treating lice. Malathion was first registered for use in the United States in 1956. What are some products that contain malathion Products containing malathion may be liquids, dusts, wettable powders, or emulsions. There are thousands of products contain- ing malathion registered for use in the United States. Always follow label instructions and take steps to avoid exposure. If any exposures occur, be sure to follow the First Aid instructions on the product label carefully. For additional treatment advice, contact the Poison Control Center at 1-800-222-1222. If you wish to discuss a pesticide problem, please call 1-800-858-7378. How does malathion work Malathion kills insects by preventing their nervous system from working properly. When healthy nerves send signals to each other, a special chemical messenger travels from one nerve to another to continue the message. The nerve signal stops when an enzyme is released into the space between the nerves. Malathion binds to the enzyme and prevents the nerve signal from stopping. This causes the nerves to signal each other without stopping. The constant nerve signals make it so the insects can’t move or breathe normally and they die. People, pets and other animals can be affected the same way as insects if they are exposed to enough malathion. -
US EPA, Pesticide Product Label, ORTHO MALATHION 50 INSECT
23V 73^ f UNITED STATES ENVIRONMENTAL PROTECTION AGENCY WASHINGTON, D.C. 20460 Jff***^ OFFICE OF WAV 00 Onit CHEMICAL SAFETY AND MAY 4 0 201] POLLUTION PREVENTION James Wallace The Scotts Company d/b/a The Ortho Group P.O.Box 190 Marysville, OH 43040 Subject: Submission of amended labeling per May 2009 Malathion RED Label Table EPA Reg. No. 239-739 Submissions dated March 5, 2010 Dear Mr. Wallace: The proposed labeling referred to above, submitted in connection with registration under the Federal Insecticide, Fungicide, and Rodenticide Act (FIFRA), is acceptable under FIFRA § 3(c)(5) provided that you submit two copies of your final printed label before you release the product for shipment. Products shipped after 12 months from the date of this amendment or the next printing of the label whichever occurs first, must bear the new revised label. Your release for shipment of the product bearing the amended label constitutes acceptance of these conditions. If these conditions are not complied with, the registration will be subject to cancellation in accordance with FIFRA sec. 6(e). The Basic Confidential Statement of Formula (CSF) dated 2/19/10 is acceptable. All other CSF's including Alternates have been superseded by this new CSF. This has been added to your record. Your product has met and complied with the risk mitigation provisions of the Malathion RED and therefore your product is reregistered pursuant to FIFRA § 4(g)(2)(C). But note, EPA is currently reassessing the cumulative impacts of organophosphates and that review may impact your product once complete. -
Malathion) Lotion, 0.5% Rx Only
NDC 51672-5276-4 Ovide® (malathion) Lotion, 0.5% Rx Only For topical use only. Not for oral or ophthalmic use. DESCRIPTION OVIDE Lotion contains 0.005 g of malathion per mL in a vehicle of isopropyl alcohol (78%), terpineol, dipentene, and pine needle oil. The chemical name of malathion is (±) - [(dimethoxyphosphinothioyl) - thio] butanedioic acid diethyl ester. Malathion has a molecular weight of 330.36, represented by C10H19O6PS2, and has the following chemical structure: CLINICAL PHARMACOLOGY Malathion is an organophosphate agent which acts as a pediculicide by inhibiting cholinesterase activity in vivo. Inadvertent transdermal absorption of malathion has occurred from its agricultural use. In such cases, acute toxicity was manifested by excessive cholinergic activity, i.e., increased sweating, salivary and gastric secretion, gastrointestinal and uterine motility, and bradycardia (see OVERDOSAGE). Because the potential for transdermal absorption of malathion from OVIDE Lotion is not known at this time, strict adherence to the dosing instructions regarding its use in children, method of application, duration of exposure, and frequency of application is required. INDICATIONS AND USAGE OVIDE Lotion is indicated for patients infected with Pediculus humanus capitis (head lice and their ova) of the scalp hair. CONTRAINDICATIONS OVIDE Lotion is contraindicated for neonates and infants because their scalps are more permeable and may have increased absorption of malathion. OVIDE Lotion should also not be used on individuals known to be sensitive to malathion or any of the ingredients in the vehicle. WARNINGS 1. OVIDE Lotion is flammable. The lotion and wet hair should not be exposed to open flames or electric heat sources, including hair dryers and electric curlers. -
162998571.Pdf
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by University of Liverpool Repository Please do not adjust margins Investigating the breakdown of the nerve agent simulant methyl paraoxon and chemical warfare agents GB and VX using nitrogen containing bases Received 00th January 20xx, Accepted 00th January 20xx Craig Wilson,a Nicholas J. Cooper,b Michael E. Briggs,a Andrew I. Cooper,*a and Dave J. Adams*c DOI: 10.1039/x0xx00000x A range of nitrogen containing bases was tested for the hydrolysis of a nerve agent simulant, methyl paraoxon (MP), and www.rsc.org/ the chemical warfare agents, GB and VX. The product distribution was found to be highly dependant on the basicity of the base and the quantity of water used for the hydrolysis. This study is important in the design of decontamination technology, which often involve mimics of CWAs. production of EA-2192 Introduction (S-(2-diisopropylaminoethyl) methylphosphonothioic acid), which exhibits roughly the same toxicity as VX itself.12 The Chemical warfare agents (CWAs) have a devastating effect on blister agent HD (Fig. 1d) can also undergo deactivation via the body and will disable or kill on exposure. Blister agents, such hydrolysis.13 However, its poor water solubility reduces the as sulfur mustard (HD, bis(2-chloroethyl) sulfide), target the skin efficiency of this decontamination method.14 As a result, and respiratory system causing severe pain and damage to the oxidation to the sulfoxide, or the addition of a co-solvent is most body whereas nerve agents, such as sarin (GB, isopropyl commonly used for HD deactivation.15-17 methylphosphonofluoridate) and VX (O-ethyl The high toxicity of CWAs means that research into their S-[2-(diisopropylamino)ethyl] methylphosphonothioate), target deactivation is often carried out using simulants. -
Chlorpyrifos (Dursban) Ddvp (Dichlorvos) Diazinon Malathion Parathion
CHLORPYRIFOS (DURSBAN) DDVP (DICHLORVOS) DIAZINON MALATHION PARATHION Method no.: 62 Matrix: Air Procedure: Samples are collected by drawing known volumes of air through specially constructed glass sampling tubes, each containing a glass fiber filter and two sections of XAD-2 adsorbent. Samples are desorbed with toluene and analyzed by GC using a flame photometric detector (FPD). Recommended air volume and sampling rate: 480 L at 1.0 L/min except for Malathion 60 L at 1.0 L/min for Malathion Target concentrations: 1.0 mg/m3 (0.111 ppm) for Dichlorvos (PEL) 0.1 mg/m3 (0.008 ppm) for Diazinon (TLV) 0.2 mg/m3 (0.014 ppm) for Chlorpyrifos (TLV) 15.0 mg/m3 (1.11 ppm) for Malathion (PEL) 0.1 mg/m3 (0.008 ppm) for Parathion (PEL) Reliable quantitation limits: 0.0019 mg/m3 (0.21 ppb) for Dichlorvos (based on the RAV) 0.0030 mg/m3 (0.24 ppb) for Diazinon 0.0033 mg/m3 (0.23 ppb) for Chlorpyrifos 0.0303 mg/m3 (2.2 ppb) for Malathion 0.0031 mg/m3 (0.26 ppb) for Parathion Standard errors of estimate at the target concentration: 5.3% for Dichlorvos (Section 4.6.) 5.3% for Diazinon 5.3% for Chlorpyrifos 5.6% for Malathion 5.3% for Parathion Status of method: Evaluated method. This method has been subjected to the established evaluation procedures of the Organic Methods Evaluation Branch. Date: October 1986 Chemist: Donald Burright Organic Methods Evaluation Branch OSHA Analytical Laboratory Salt Lake City, Utah 1 of 27 T-62-FV-01-8610-M 1. -
Full Page Fax Print
RESISTANCE TO MALATHION, PIRIMIPHOS-METHYL AND FENITROTHION IN COLEOPTERA FROM STORED GRAINS. Ivania A. PACHECO; M. Regina SARTORI; Scheilla BOLONHEZI Instituto de Tecnologia de Alimentos Avenida Brasil, 2880 - Caixa Postal 139 Campinas - Sao Paulo - Brasil - CEP 13073 SUMMARY The objectives of this paper were:l) to verify the occurrance of resistance to malathion, pirimiphos-methyl and fenitrothion in populations of coleoptera from stored grains and 2) to obtain data that could contribute to the adequate control of these insects during storage, thus reducing losses. Populations of Sitophilus oryzae, ~. zeamais, Tribolium castaneum and Rhyzopertha dominica were collected from storage facilities located in different regions of Brazil, and tested for resistance to the tree insecticides according to the FAO Standard Method (FAO, 1975). Insects were collected in the States of Sao Paulo, Rio Grande do SuI, Santa Catarina, Goias, Acre and Rondonia. Twenty populations of S. oryzae, ten of S. zeamais, twenty of R. dominica and twenty -five of T. castan~ad already been tested for - resistance to the three insecticides. Seven populations of S. oryzae, six of R. dominica and ten of S. zean~is were susceptible 'to the th~ee insecticides. Resistance to malathion was showed in thirteen populations of S. oryzae, fourteen of ~. dominica and twenty-five of !. castaneum. Simultaneous cross-resistance to pirimiphos-methyl and fenitrothion was indicated in one population of ~. oryzae and eight of !. castaneum. Cross resistance only to pirimiphos-methyl was indicated in two populations of ~. oryzae, one of ~. dominica and one of !. castaneum and only to fenitrothion in two of R. dominica and two of T. -
Chemical Name Federal P Code CAS Registry Number Acutely
Acutely / Extremely Hazardous Waste List Federal P CAS Registry Acutely / Extremely Chemical Name Code Number Hazardous 4,7-Methano-1H-indene, 1,4,5,6,7,8,8-heptachloro-3a,4,7,7a-tetrahydro- P059 76-44-8 Acutely Hazardous 6,9-Methano-2,4,3-benzodioxathiepin, 6,7,8,9,10,10- hexachloro-1,5,5a,6,9,9a-hexahydro-, 3-oxide P050 115-29-7 Acutely Hazardous Methanimidamide, N,N-dimethyl-N'-[2-methyl-4-[[(methylamino)carbonyl]oxy]phenyl]- P197 17702-57-7 Acutely Hazardous 1-(o-Chlorophenyl)thiourea P026 5344-82-1 Acutely Hazardous 1-(o-Chlorophenyl)thiourea 5344-82-1 Extremely Hazardous 1,1,1-Trichloro-2, -bis(p-methoxyphenyl)ethane Extremely Hazardous 1,1a,2,2,3,3a,4,5,5,5a,5b,6-Dodecachlorooctahydro-1,3,4-metheno-1H-cyclobuta (cd) pentalene, Dechlorane Extremely Hazardous 1,1a,3,3a,4,5,5,5a,5b,6-Decachloro--octahydro-1,2,4-metheno-2H-cyclobuta (cd) pentalen-2- one, chlorecone Extremely Hazardous 1,1-Dimethylhydrazine 57-14-7 Extremely Hazardous 1,2,3,4,10,10-Hexachloro-6,7-epoxy-1,4,4,4a,5,6,7,8,8a-octahydro-1,4-endo-endo-5,8- dimethanonaph-thalene Extremely Hazardous 1,2,3-Propanetriol, trinitrate P081 55-63-0 Acutely Hazardous 1,2,3-Propanetriol, trinitrate 55-63-0 Extremely Hazardous 1,2,4,5,6,7,8,8-Octachloro-4,7-methano-3a,4,7,7a-tetra- hydro- indane Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]- 51-43-4 Extremely Hazardous 1,2-Benzenediol, 4-[1-hydroxy-2-(methylamino)ethyl]-, P042 51-43-4 Acutely Hazardous 1,2-Dibromo-3-chloropropane 96-12-8 Extremely Hazardous 1,2-Propylenimine P067 75-55-8 Acutely Hazardous 1,2-Propylenimine 75-55-8 Extremely Hazardous 1,3,4,5,6,7,8,8-Octachloro-1,3,3a,4,7,7a-hexahydro-4,7-methanoisobenzofuran Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime 26419-73-8 Extremely Hazardous 1,3-Dithiolane-2-carboxaldehyde, 2,4-dimethyl-, O- [(methylamino)-carbonyl]oxime. -
Lifetime Organophosphorous Insecticide Use Among Private Pesticide Applicators in the Agricultural Health Study
Journal of Exposure Science and Environmental Epidemiology (2012) 22, 584 -- 592 & 2012 Nature America, Inc. All rights reserved 1559-0631/12 www.nature.com/jes ORIGINAL ARTICLE Lifetime organophosphorous insecticide use among private pesticide applicators in the Agricultural Health Study Jane A. Hoppin1, Stuart Long2, David M. Umbach3, Jay H. Lubin4, Sarah E. Starks5, Fred Gerr5, Kent Thomas6, Cynthia J. Hines7, Scott Weichenthal8, Freya Kamel1, Stella Koutros9, Michael Alavanja9, Laura E. Beane Freeman9 and Dale P. Sandler1 Organophosphorous insecticides (OPs) are the most commonly used insecticides in US agriculture, but little information is available regarding specific OP use by individual farmers. We describe OP use for licensed private pesticide applicators from Iowa and North Carolina in the Agricultural Health Study (AHS) using lifetime pesticide use data from 701 randomly selected male participants collected at three time periods. Of 27 OPs studied, 20 were used by 41%. Overall, 95% had ever applied at least one OP. The median number of different OPs used was 4 (maximum ¼ 13). Malathion was the most commonly used OP (74%) followed by chlorpyrifos (54%). OP use declined over time. At the first interview (1993--1997), 68% of participants had applied OPs in the past year; by the last interview (2005--2007), only 42% had. Similarly, median annual application days of OPs declined from 13.5 to 6 days. Although OP use was common, the specific OPs used varied by state, time period, and individual. Much of the variability in OP use was associated with the choice of OP, rather than the frequency or duration of application. -
Background Information for Chlorpyrifos
64 Appendix A: Background Information for Chlorpyrifos Chlorpyrifos is an organophosphorus insecticide. It belongs to the phosphorothioate (also called phosphorothionate) group, composed of organophosphorus compounds that contain the P=S substructure. Other organophosphorus insecticides in this group include diazinon, methyl parathion, parathion, fenthion, and fenitrothion. These compounds require metabolic activation to their oxon analogs (compounds in which the =S is replaced by =O) for anticholinesterase activity. The structures of chlorpyrifos and its toxic metabolite, chlorpyrifos oxon, are provided in Appendix D. As of 2000, chlorpyrifos was one of the most widely used organophosphorus insecticides in the United States, for both agricultural and residential purposes. Registered uses included food crops, turf and ornamental plants, indoor pest control (including crack and crevice treatment), termite control, mosquito control, and pet collars. It was registered for use in a wide variety of buildings, including residential, commercial, schools, daycare centers, restaurants, hospitals, hotels, and food manufacturing plants (EPA 2000c). Many uses of chlorpyrifos are being phased out (see Section A.4). A study of urinary pesticide metabolites during the third trimester in 386 pregnant women from East Harlem indicated that exposure to chlorpyrifos was prevalent (42% of the women had detectable levels of the chlorpyrifos metabolite), was higher than the median in NHANES III, did not show seasonal variation, and did not change during the