Protecting Honey Bees from Pesticides
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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, -
2,4-Dichlorophenoxyacetic Acid
2,4-Dichlorophenoxyacetic acid 2,4-Dichlorophenoxyacetic acid IUPAC (2,4-dichlorophenoxy)acetic acid name 2,4-D Other hedonal names trinoxol Identifiers CAS [94-75-7] number SMILES OC(COC1=CC=C(Cl)C=C1Cl)=O ChemSpider 1441 ID Properties Molecular C H Cl O formula 8 6 2 3 Molar mass 221.04 g mol−1 Appearance white to yellow powder Melting point 140.5 °C (413.5 K) Boiling 160 °C (0.4 mm Hg) point Solubility in 900 mg/L (25 °C) water Related compounds Related 2,4,5-T, Dichlorprop compounds Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) 2,4-Dichlorophenoxyacetic acid (2,4-D) is a common systemic herbicide used in the control of broadleaf weeds. It is the most widely used herbicide in the world, and the third most commonly used in North America.[1] 2,4-D is also an important synthetic auxin, often used in laboratories for plant research and as a supplement in plant cell culture media such as MS medium. History 2,4-D was developed during World War II by a British team at Rothamsted Experimental Station, under the leadership of Judah Hirsch Quastel, aiming to increase crop yields for a nation at war.[citation needed] When it was commercially released in 1946, it became the first successful selective herbicide and allowed for greatly enhanced weed control in wheat, maize (corn), rice, and similar cereal grass crop, because it only kills dicots, leaving behind monocots. Mechanism of herbicide action 2,4-D is a synthetic auxin, which is a class of plant growth regulators. -
Herbicide Mode of Action Table High Resistance Risk
Herbicide Mode of Action Table High resistance risk Chemical family Active constituent (first registered trade name) GROUP 1 Inhibition of acetyl co-enzyme A carboxylase (ACC’ase inhibitors) clodinafop (Topik®), cyhalofop (Agixa®*, Barnstorm®), diclofop (Cheetah® Gold* Decision®*, Hoegrass®), Aryloxyphenoxy- fenoxaprop (Cheetah®, Gold*, Wildcat®), fluazifop propionates (FOPs) (Fusilade®), haloxyfop (Verdict®), propaquizafop (Shogun®), quizalofop (Targa®) Cyclohexanediones (DIMs) butroxydim (Factor®*), clethodim (Select®), profoxydim (Aura®), sethoxydim (Cheetah® Gold*, Decision®*), tralkoxydim (Achieve®) Phenylpyrazoles (DENs) pinoxaden (Axial®) GROUP 2 Inhibition of acetolactate synthase (ALS inhibitors), acetohydroxyacid synthase (AHAS) Imidazolinones (IMIs) imazamox (Intervix®*, Raptor®), imazapic (Bobcat I-Maxx®*, Flame®, Midas®*, OnDuty®*), imazapyr (Arsenal Xpress®*, Intervix®*, Lightning®*, Midas®* OnDuty®*), imazethapyr (Lightning®*, Spinnaker®) Pyrimidinyl–thio- bispyribac (Nominee®), pyrithiobac (Staple®) benzoates Sulfonylureas (SUs) azimsulfuron (Gulliver®), bensulfuron (Londax®), chlorsulfuron (Glean®), ethoxysulfuron (Hero®), foramsulfuron (Tribute®), halosulfuron (Sempra®), iodosulfuron (Hussar®), mesosulfuron (Atlantis®), metsulfuron (Ally®, Harmony®* M, Stinger®*, Trounce®*, Ultimate Brushweed®* Herbicide), prosulfuron (Casper®*), rimsulfuron (Titus®), sulfometuron (Oust®, Eucmix Pre Plant®*, Trimac Plus®*), sulfosulfuron (Monza®), thifensulfuron (Harmony®* M), triasulfuron (Logran®, Logran® B-Power®*), tribenuron (Express®), -
Exposure to Herbicides in House Dust and Risk of Childhood Acute Lymphoblastic Leukemia
Journal of Exposure Science and Environmental Epidemiology (2013) 23, 363–370 & 2013 Nature America, Inc. All rights reserved 1559-0631/13 www.nature.com/jes ORIGINAL ARTICLE Exposure to herbicides in house dust and risk of childhood acute lymphoblastic leukemia Catherine Metayer1, Joanne S. Colt2, Patricia A. Buffler1, Helen D. Reed3, Steve Selvin1, Vonda Crouse4 and Mary H. Ward2 We examine the association between exposure to herbicides and childhood acute lymphoblastic leukemia (ALL). Dust samples were collected from homes of 269 ALL cases and 333 healthy controls (o8 years of age at diagnosis/reference date and residing in same home since diagnosis/reference date) in California, using a high-volume surface sampler or household vacuum bags. Amounts of agricultural or professional herbicides (alachlor, metolachlor, bromoxynil, bromoxynil octanoate, pebulate, butylate, prometryn, simazine, ethalfluralin, and pendimethalin) and residential herbicides (cyanazine, trifluralin, 2-methyl-4- chlorophenoxyacetic acid (MCPA), mecoprop, 2,4-dichlorophenoxyacetic acid (2,4-D), chlorthal, and dicamba) were measured. Odds ratios (OR) and 95% confidence intervals (CI) were estimated by logistic regression. Models included the herbicide of interest, age, sex, race/ethnicity, household income, year and season of dust sampling, neighborhood type, and residence type. The risk of childhood ALL was associated with dust levels of chlorthal; compared to homes with no detections, ORs for the first, second, and third tertiles were 1.49 (95% CI: 0.82–2.72), 1.49 (95% CI: 0.83–2.67), and 1.57 (95% CI: 0.90–2.73), respectively (P-value for linear trend ¼ 0.05). The magnitude of this association appeared to be higher in the presence of alachlor. -
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 -
Appendix a Analysis of Products with Two Or More Active Ingredients
APPENDIX A ANALYSIS OF PRODUCTS WITH TWO OR MORE ACTIVE INGREDIENTS The Agency does not routinely include, in its risk assessments, an evaluation of mixtures of active ingredients, either those mixtures of multiple active ingredients in product formulations or those in the applicator’s tank. In the case of the product formulations of active ingredients (that is, a registered product containing more than one active ingredient), each active ingredient is subject to an individual risk assessment for regulatory decision regarding the active ingredient on a particular use site. If effects data are available for a formulated product containing more than one active ingredient, they may be used qualitatively or quantitatively1 2. There are no product LD50 values, with associated 95% Confidence Intervals (CIs) available for glyphosate. As discussed in USEPA (2000) a quantitative component-based evaluation of mixture toxicity requires data of appropriate quality for each component of a mixture. In this mixture evaluation an LD50 with associated 95% CI is needed for the formulated product. The same quality of data is also required for each component of the mixture. Given that the formulated products for glyphosate do not have LD50 data available it is not possible to undertake a quantitative or qualitative analysis for potential interactive effects. However, because the active ingredients are not expected to have similar mechanisms of action, metabolites, or toxicokinetic behavior, it is reasonable to conclude that an assumption of dose-addition would be inappropriate. Consequently, an assessment based on the toxicity of glyphosate is the only reasonable approach that employs the available data to address the potential acute risks of the formulated products. -
California Restricted Materials Requirements (English)
CALIFORNIA RESTRICTED MATERIALS REQUIREMENTS FEDERAL RESTRICTED USE PESTICIDES RESTRICTED USE PESTICIDE A (Included by reference as California Restricted Materials) DUE TO (reason for restricted use classification) Pesticides display the RESTRICTED USE PESTICIDE (RUP) statement on For retail sale to and use only by Certified Applicators or the pesticide container similar to the statement shown here. RUPs require an persons under their direct supervision and only for those RUP statement enclosed in a box, at the top of the front panel of the label. uses covered by the Certified Applicator's certification. Some product labels require a Certified Applicator be “physically present” at the use site. B CALIFORNIA RESTRICTED MATERIALS This section is written in a quick reference format; refer to Title 3, California Code of Regulations (3 CCR) section 6400 for complete text. Acrolein, labeled for use as an aquatic Chlorpyrifos, labeled for the Metam sodium, labeled for the Potassium n-methyldithiocarbamate herbicide production of an agricultural production of agricultural plant (metam-potassium), labeled for the Aldicarb – unregistered commodity commodities production of agricultural plant All dust (except products containing Dazomet, labeled for the production Methamidophos – unregistered commodities only exempt pesticides)** of agricultural plant commodities Methidathion Propanil (3,4-dichloropropionanilide) Aluminum phosphide Dicamba* Methomyl†† Sodium cyanide Any pesticide containing active 2,4-dichlorophenoxyacetic acid Methyl bromide Sodium -
Ten Reasons Not to Use Pesticides
JOURNAL OF PESTICIDE REFORM/ SUMMER 2006 • VOL. 26, NO. 2 PESTICIDE BASICS contaminated with pesticides. They play in ways that in- crease their exposure. Also, their growing bodies can be Ten Reasons Not to Use particularly sensitive. EPA succinctly summarizes the reasons why children should not be Pesticides exposed to pesticides: • their internal organs are still BY CAROLINE COX has written, “the range of these adverse developing and maturing, health effects includes acute and persis- • in relation to their body weight, tent injury to the nervous system, lung infants and children eat and drink damage, injury to reproductive organs, more than adults, possibly increasing 1. Pesticides don’t solve pest dysfunction of the immune and endo- problems. They don’t change their exposure to pesticides in food crine [hormone] systems, birth defects, and water. the conditions that encourage and cancer.”3 pests. • certain behaviors--such as play- Pesticides that damage human ing on floors or lawns or putting Some pesticides are remarkably ef- health are used in staggering amounts. objects in their mouths—increase a ficient tools for killing pests, but almost Consider just the 27 most commonly 4 child’s exposure to pesticides used in all do nothing to solve pest problems. used pesticides. Fifteen of these have 8 5 homes and yards. To solve a pest problem, the most been classified as carcinogens by EPA Researchers continue to gather de- important step is to change the con- and their use totals about 300 million 4 tailed evidence that EPA’s concerns ditions that have allowed the pest to pounds every year. -
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 -
Advances in Enzyme-Based Biosensors for Pesticide Detection
biosensors Review Advances in Enzyme-Based Biosensors for Pesticide Detection Bogdan Bucur 1 ID , Florentina-Daniela Munteanu 2 ID , Jean-Louis Marty 3,* and Alina Vasilescu 4 ID 1 National Institute of Research and Development for Biological Sciences, Centre of Bioanalysis, 296 Splaiul Independentei, 060031 Bucharest, Romania; [email protected] 2 Faculty of Food Engineering, Tourism and Environmental Protection, “Aurel Vlaicu” University of Arad, Elena Dragoi, No. 2, 310330 Arad, Romania; fl[email protected] 3 BAE Laboratory, Université de Perpignan via Domitia, 52 Avenue Paul Alduy, 66860 Perpignan, France 4 International Centre of Biodynamics, 1B Intrarea Portocalelor, 060101 Bucharest, Romania; [email protected] * Correspondence: [email protected]; Tel.: +33-468-66-1756 Received: 28 February 2018; Accepted: 20 March 2018; Published: 22 March 2018 Abstract: The intensive use of toxic and remanent pesticides in agriculture has prompted research into novel performant, yet cost-effective and fast analytical tools to control the pesticide residue levels in the environment and food. In this context, biosensors based on enzyme inhibition have been proposed as adequate analytical devices with the added advantage of using the toxicity of pesticides for detection purposes, being more “biologically relevant” than standard chromatographic methods. This review proposes an overview of recent advances in the development of biosensors exploiting the inhibition of cholinesterases, photosynthetic system II, alkaline phosphatase, cytochrome P450A1, peroxidase, tyrosinase, laccase, urease, and aldehyde dehydrogenase. While various strategies have been employed to detect pesticides from different classes (organophosphates, carbamates, dithiocarbamates, triazines, phenylureas, diazines, or phenols), the number of practical applications and the variety of environmental and food samples tested remains limited. -
12 Chemical Fact Sheets
1212 ChemicalChemical factfact sheetssheets A conceptual framework for Introduction implementing the Guidelines (Chapter 1) (Chapter 2) he background docudocu-- ments referred to in FRAMEWORK FOR SAFE DRINKING-WATER SUPPORTING Tments referred to in INFORMATION thisthis chapterchapter (as the princi-princi- Health-based targets Public health context Microbial aspects pal reference for each fact (Chapter 3) and health outcome (Chapters 7 and 11) sheet) may be found on Water safety plans Chemical aspects (Chapter 4) (Chapters 8 and 12) thethe Water, Sanitation, HyHy-- System Management and Radiological Monitoring giene and Health web site assessment communication aspects at http://www.who.int/ (Chapter 9) Acceptability Surveillance water_sanitation_health/ aspects (Chapter 5) dwq/chemicals/en/indewater-quality/guidelines/x. (Chapter 10) htmlchemicals/en/. A complete. A complete list of rlist eferences of references cited citedin this in Application of the Guidelines in specic circumstances chapter,this chapter, including including the (Chapter 6) background documents Climate change, Emergencies, Rainwater harvesting, Desalination forfor each cchemical, hemical, is pro-pro- systems, Travellers, Planes and vided in Annex 22.. ships, etc. 12.1 Chemical contaminants in drinking-water Acrylamide Residual acrylamideacrylamide monomermonomer occursoccurs inin polyacrylamidepolyacrylamide coagulantscoagulants used used in in thethe treattreat-- ment of drinking-water. In general, thethe maximummaximum authorizedauthorized dosedose ofof polymerpolymer isis 11 mg/l. mg/l. At a monomer content of 0.05%, this corresponds to a maximum theoretical concen-- trationtration ofof 0.5 µg/l of the monomer in water.water. Practical concentrations maymay bebe lowerlower byby aa factor factor of 2–3. This applies applies to to thethe anionic anionic and and non-ionic non-ionic polyacrylamides, polyacrylamides, but but residual residual levelslevels fromfrom cationic polyacrylamides maymay bebe higher.higher. -
Developmental Ramifications of Dithiocarbamate Pesticide Exposure in Zebrafish
AN ABSTRACT OF THE DISSERTATION OF Fred Tilton for the degree of Doctor of Philosophy in Toxicology presented on May 24, 2006. Title:Developmental Ramifications of Dithiocarbamate Pesticide Exposure in Zebrafish. Redacted for Privacy Abstract approved Robert Dithiocarbamates are widely used agricultural pesticides, industrial chemicals and effluent additives. DTCs and their related compounds have historical and current relevance in clinical and experimental medicine. DTC developmental toxicity is well established, but poorly understood. Dithiocarbamates according to the U.S. EPA have a mechanism of action involving, "the inhibition of metal-dependent and sulfhydryl enzyme systems in fungi, bacteria, plants, as well as mammals." We hypothesized that by using the zebrafish development model we could better define the mechanism of action of DTCs and for the first time establish a molecular understanding of DTC developmental toxicity in vertebrates. We have established that all types of dithiocarbamate pesticides and some degradation products have the potential to elicit a common toxic effect on development resulting in a distorted notochord and a significant impact to the body axis. We provide evidence to support the hypothesis that metal chelation is not the primary mechanism of action by which DTCs impact the developing vertebrate. By manipulating the exposure window of zebrafish we hypothesized that somitogenesis was the targeted developmental process. We tested this by using the Affymetrix microarray to observe gene expression induced by the N-methyl dithiocarbamate, metam sodium (NaM). Throughout this process it is clear that genes related to muscle development are perturbed. These gene signatures are consistent with the morphological changes observed in larval and adult animals and that somitogenesis is the developmental target.