Redalyc.Correlation Between 2,4-D Herbicide Residues and Soil Attributes in Southern of Brazil
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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. -
PPO2 Mutations in Amaranthus Palmeri:Implications on Cross-Resistance
agriculture Article PPO2 Mutations in Amaranthus palmeri: Implications on Cross-Resistance Pâmela Carvalho-Moore 1,2 , Gulab Rangani 1, James Heiser 3, Douglas Findley 4, Steven J. Bowe 4 and Nilda Roma-Burgos 1,* 1 Department of Crop, Soil and Environmental Sciences, University of Arkansas, Fayetteville, AR 72704, USA; [email protected] (P.C.-M.); [email protected] (G.R.) 2 Former Cell and Molecular Biology Program, University of Arkansas, Fayetteville, AR 72704, USA 3 Fisher Delta Research Center, College of Agriculture, University of Missouri, Portageville, MO 63873, USA; [email protected] 4 BASF Corporation, Research Triangle Park, NC 27709, USA; douglas.fi[email protected] (D.F.); [email protected] (S.J.B.) * Correspondence: [email protected] Abstract: In Arkansas, resistance to protoporphyrinogen IX oxidase (PPO)-inhibiting herbicides in Amaranthus palmeri S. Wats. is mainly due to target site mutations. Although A. palmeri PPO-mutations are well investigated, the cross-resistance that each ppo mutant endows to weed populations is not yet well understood. We aimed to evaluate the response of PPO-resistant A. palmeri accessions, harboring the ppo2 mutations DG210 and G399A, to multiple PPO-inhibiting herbicides. Six resistant and one susceptible field accessions were subjected to a dose–response assay with fomesafen, and selected survivors from different fomesafen doses were genotyped to characterize the mutation profile. The level of resistance to fomesafen was determined and a cross-resistance assay was conducted with 1 Citation: Carvalho-Moore, P.; and 2 times the labeled doses of selected PPO herbicides. The accession with higher predicted dose Rangani, G.; Heiser, J.; Findley, D.; to control 50% of the population (ED50) had a higher frequency of DG210-homozygous survivors. -
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®), -
Weed Control in Direct-Seeded Field Pea Gregory J
Weed Control in Direct-seeded Field Pea Gregory J. Endres and Blaine G. Schatz Weed control and field pea response to selected soil- and POST-applied herbicides were evaluated in a randomized complete-block design with three replicates. The experiment was conducted on a Heimdahl loam soil with 6.7 pH and 2.9% organic matter at the NDSU Carrington Research Extension Center. Herbicide treatments were applied to 5- by 25-ft plots with a pressurized hand-held plot sprayer at 17 gal/A and 30 psi through 8002 flat-fan nozzles. Fall sulfentrazone treatments were applied October 25, 2004 to a moist soil surface with 47 F, 71% RH, 15% clear sky, and 11 mph wind. On April 28, 2005, inoculated 'Integra' field pea was seeded into standing wheat stubble in 7-inch rows at a rate of 300,000 pure live seeds/A. PRE treatments were applied to a dry soil surface on April 30 with 31 F, 64% RH, 30% clear sky, and 10 mph wind. Rainfall totaled 1.22 inches 8 d following PRE application. The trial area was treated on May 6 with a PRE burn-down application of glyphosate at 0.75 lb ae/A plus ammonium sulfate at 1% v/v. The early POST (EPOST) treatment was applied on May 23 with 73 F, 35% RH, 100% cloudy sky, and 6 mph wind to 2-inch tall field pea, 1- to 2-leaf green and yellow foxtail, 0.5-inch tall common lambsquarters, 0.5-inch tall prostrate and redroot pigweed, and 0.5-inch tall wild buckwheat. -
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 -
RR Program's RCL Spreadsheet Update
RR Program’s RCL Spreadsheet Update March 2017 RR Program RCL Spreadsheet Update DNR-RR-052e The Wisconsin DNR Remediation and Redevelopment Program (RR) has updated the numerical soil standards in the August 2015 DNR-RR- 052b RR spreadsheet of residual contaminant levels (RCLs). The RCLs were determined using the U.S. EPA RSL web- calculator by accepting EPA exposure defaults, with the exception of using Chicago, IL, for the climatic zone. This documentThe U.S. provides EPA updateda summary its Regionalof changes Screening to the direct-contact Level (RSL) RCLs website (DC-RCLs) in June that2015. are To now reflect in the that March 2017 spreadsheet.update, the The Wisconsin last page ofDNR this updated document the has numerical the EPA exposuresoil standards, parameter or residual values usedcontaminant in the RCL levels calculations. (RCLs), in the Remediation and Redevelopment program’s spreadsheet of RCLs. This document The providesU.S. EPA a RSL summary web-calculator of the updates has been incorporated recently updated in the Julyso that 2015 the spreadsheet.most up-to-date There toxicity were values no changes for chemi - cals madewere certainlyto the groundwater used in the RCLs,RCL calculations. but there are However, many changes it is important in the industrial to note that and the non-industrial web-calculator direct is only a subpartcontact of the (DC) full RCLsEPA RSL worksheets. webpage, Tables and that 1 andthe other 2 of thissubparts document that will summarize have important the DC-RCL explanatory changes text, generic tablesfrom and the references previous have spreadsheet yet to be (Januaryupdated. -
US EPA, Pesticide Product Label, A335.06,09/21/2020
[Note to reviewer: [Text] in brackets denotes optional or explanatory language [Note to reviewer: {Text} in braces denotes where in the final label text will appear {BOOKLET FRONT PANEL LANGUAGE} S-METOLACHLOR GROUP 15 HERBICIDE METRIBUZIN GROUP 5 HERBICIDE FOMESAFEN GROUP 14 HERBICIDE A335.06[™] [Alternate Brand Name: Statler] [Herbicide for preemergent control of certain grasses and broadleaf weeds in Soybeans] ACTIVE INGREDIENTS: (% by weight) S-Metolachlor*………………………………………….……………………………………………………………………………..…………………… 36.29% Metribuzin**………………………………………….……………………………………………………………………………..………………………. 8.05% Fomesafen***………………………………………….……………………………………………………………………………..……………………... 7.16% OTHER INGREDIENTS: ……………………………………………………..…………………………………………………………………………….. 48.5% TOTAL …………………………………………………………………………………………………………….……………………………………………. 100.0% *contains 3.39 Ib of S-metolachlor per gallon **contains 0.75 Ib of metribuzin per gallon ***contains 0.67 Ib of fomesafen acid per gallon KEEP OUT OF REACH OF CHILDREN CAUTION Si usted no entiende la etiqueta, busque a alguien para que se la explique a usted en detalle. (If you do not understand the label, find someone to explain it to you in detail.) See [below] [inside label booklet] for [additional] [First Aid,] [Precautionary Statements] and [Directions for Use]. EPA Reg. No.: 91234-201 EPA Est. No.: Net Weight: Manufactured for: Atticus, LLC 5000 CentreGreen Way, Suite 100 Cary, NC 27513 1 {LANGUAGE INSIDE BOOKLET} FIRST AID If on skin or Take off contaminated clothing. clothing: Rinse skin immediately with plenty of water for 15-20 minutes. Call a poison control center or doctor for treatment advice. If swallowed: Call a poison control center or doctor immediately for treatment advice. Have person sip a glass of water if able to swallow. Do not induce vomiting unless told to do so by the poison control center or doctor. -
Thickening Glyphosate Formulations
(19) TZZ _T (11) EP 2 959 777 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 30.12.2015 Bulletin 2015/53 A01N 57/20 (2006.01) A01N 25/30 (2006.01) A01P 13/00 (2006.01) (21) Application number: 15175726.7 (22) Date of filing: 17.08.2009 (84) Designated Contracting States: (71) Applicant: Akzo Nobel N.V. AT BE BG CH CY CZ DE DK EE ES FI FR GB GR 6824 BM Arnhem (NL) HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR (72) Inventor: ZHU, Shawn Stormville, NY New York 12582 (US) (30) Priority: 19.08.2008 US 90010 P 09.09.2008 EP 08163910 (74) Representative: Akzo Nobel IP Department Velperweg 76 (62) Document number(s) of the earlier application(s) in 6824 BM Arnhem (NL) accordance with Art. 76 EPC: 11191518.7 / 2 425 716 Remarks: 09781884.3 / 2 315 524 This application was filed on 07-07-2015 as a divisional application to the application mentioned under INID code 62. (54) THICKENING GLYPHOSATE FORMULATIONS (57) The present invention generally relates to a glyphosate formulation with enhanced viscosity, said formulation containing a thickening composition comprising at least one nitrogen- containing surfactant. EP 2 959 777 A1 Printed by Jouve, 75001 PARIS (FR) EP 2 959 777 A1 Description FIELD OF THE INVENTION 5 [0001] The present invention relates to a glyphosate formulations thickened by nitrogen containing surfactants. BACKGROUND OF THE INVENTION [0002] Glyphosate is the most widely used herbicide in the world. -
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 -
CLARC Excerpt
Washington State Department of Ecology - CLARC Air Table (Methods B and C) - February 2021 February 2021 S S CPFi S CPFo S Air Air RfC o RfDi o Inhalation RfDo o Oral o Air Air Method C Method C Inhalation u Inhalation IUR u Cancer Oral u Cancer u Method B Method B Noncancer Cancer Reference Reference Inhalation Potency Reference Potency Noncancer Cancer (Eq. 750-1 (Eq. 750-2 Chemical Data Links to r r r r Concentration c Dose Unit Risk c Factor Dose c Factor c (Eq. 750-1) (Eq. 750-2) adjusted) adjusted) 3 3 -1 CAS No. Group Chemical Name Important Notes (mg/m ) e (mg/kg-day) (µg/m ) e (kg-day/mg) (mg/kg-day) e (kg-day/mg) e (µg/m³) (µg/m³) (µg/m³) (µg/m³) 83-32-9 PAHs acenaphthene 6.00E-02 I 30560-19-1 Pesticides acephate 1.20E-03 O 75-07-0 VOCs acetaldehyde 9.00E-03 I 2.57E-03 2.20E-06 I 7.70E-03 4.10E+00 1.10E+00 9.00E+00 1.10E+01 34256-82-1 Pesticides acetochlor 2.00E-02 I 67-64-1 VOCs acetone 3.10E+01 A 8.86E+00 9.00E-01 I 1.40E+04 3.10E+04 75-86-5 VOCs acetone cyanohydrin 2.00E-03 X 5.71E-04 9.10E-01 2.00E+00 75-05-8 VOCs acetonitrile 6.00E-02 I 1.71E-02 2.70E+01 6.00E+01 98-86-2 SVOCs acetophenone 1.00E-01 I 62476-59-9 Herbicides acifluorfen, sodium 1.30E-02 I 107-02-8 VOCs acrolein 2.00E-05 I 5.71E-06 5.00E-04 I 9.10E-03 2.00E-02 79-06-1 VOCs acrylamide 6.00E-03 I 1.71E-03 1.00E-04 I-M 3.50E-01 2.00E-03 I 5.00E-01 I-M 2.70E+00 6.60E-03 6.00E+00 2.50E-01 79-10-7 VOCs acrylic acid 1.00E-03 I 2.86E-04 5.00E-01 I 4.60E-01 1.00E+00 107-13-1 VOCs acrylonitrile 2.00E-03 I 5.71E-04 6.80E-05 I 2.38E-01 4.00E-02 A 5.40E-01 I 9.10E-01 3.70E-02 -
Nozzle Selection and Adjuvant Impact on the Efficacy of Glyphosate And
agronomy Article Nozzle Selection and Adjuvant Impact on the Efficacy of Glyphosate and PPO-Inhibiting Herbicide Tank-Mixtures Jesaelen G. Moraes 1,* , Thomas R. Butts 1 , Vitor M. Anunciato 2 , Joe D. Luck 3 , Wesley C. Hoffmann 4, Ulisses R. Antuniassi 5 and Greg R. Kruger 1 1 Department of Agronomy and Horticulture, University of Nebraska-Lincoln, North Platte, NE 69101, USA; [email protected] (T.R.B.); [email protected] (G.R.K.) 2 Department of Plant Protection, Sao Paulo State University, Botucatu, SP 18618687, Brazil; [email protected] 3 Department of Biological System Engineering, University of Nebraska-Lincoln, North Platte, NE 69101, USA; [email protected] 4 USDA-ARS Aerial Application Technology Research Unit, College Station, TX 77845, USA; [email protected] 5 Department of Rural Engineering, Sao Paulo State University, Botucatu, SP 18618687, Brazil; [email protected] * Correspondence: [email protected]; Tel.: +1-402-219-1674 Abstract: PPO-inhibiting herbicides in combination with glyphosate for postemergence applications is a common approach to manage glyphosate- and ALS-inhibitor-resistant weeds. PPO-inhibitors can reduce glyphosate translocation when applied in tank-mixtures, but adjuvants may be used to overcome this effect. Additionally, optimal droplet size may be affected by tank-mixtures of different Citation: Moraes, J.G.; Butts, T.R.; herbicides and it can be crucial to herbicide efficacy. Field and greenhouse studies were conducted M. Anunciato, V.; Luck, J.D.; to investigate the impact of nozzle selection and adjuvants on weed control and interactions when Hoffmann, W.C.; Antuniassi, U.R.; applying PPO-inhibitors (fomesafen or lactofen) alone or in tank-mixture with glyphosate to five Kruger, G.R. -
Sulfentrazone 4L
SPECIMEN LABEL SULFENTRAZONE GROUP 14 HERBICIDE SULFENTRAZONE 4L ACTIVE INGREDIENT: Sulfentrazone . 40.4% Manufactured for: OTHER INGREDIENTS: .................................................. 60.6% TOTAL: ............................................................. 100.0% ALBAUGH, LLC Contains 4 pounds of active ingredient per gallon. EPA Reg. No. 42750-357 EPA Est. No. 42750-MO-01 1525 NE 36th Street KEEP OUT OF REACH OF CHILDREN Ankeny, Iowa 50021 CAUTION Si usted no entiende seta etiqueta, busque a alguien para que se la explique a usted en detalle, (If you do not understand this label, find someone to explain it to you in detail.) FOR CHEMICAL SPILL, LEAK, FIRST AID FIRE, OR EXPOSURE, CALL IF SWALLOWED • Call a poison control center or doctor immediately for treatment advice. CHEMTREC 1-800-424-9300 • Have person sip a glass of water if able to swallow. • Do not induce vomiting unless told to do so by the poison control center or doctor. • Do not give anything by mouth to an unconscious person. IF INHALED • Move person to fresh air. • If person is not breathing, call 911 or an ambulance, then give artificial respiration, preferably by mouth-to-mouth, if possible. • Call a poison control center or doctor for further treatment advice. IF ON SKIN OR • Take off contaminated clothing. CLOTHING: • Rinse skin immediately with plenty of water for 15-20 minutes. • Call a Poison Control Center or doctor for treatment advice. IF IN EYES • Hold eye open and rinse slowly and gently with water for 15-20 minutes. • Remove contact lenses, if present, after the first 5 minutes. Then continue rinsing eye. • Call a Poison Control Center or doctor for treatment advice.