WO2010046268A2 - Procédé de contrôle de l'arbre à suif - Google Patents

Procédé de contrôle de l'arbre à suif Download PDF

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Publication number
WO2010046268A2
WO2010046268A2 PCT/EP2009/063303 EP2009063303W WO2010046268A2 WO 2010046268 A2 WO2010046268 A2 WO 2010046268A2 EP 2009063303 W EP2009063303 W EP 2009063303W WO 2010046268 A2 WO2010046268 A2 WO 2010046268A2
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WO
WIPO (PCT)
Prior art keywords
inhibitors
imazamox
chinese tallowtree
herbicide
herbicides
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Application number
PCT/EP2009/063303
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English (en)
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WO2010046268A3 (fr
Inventor
Daniel D. Beran
Wayne Ducote
Alane J-Bo Burns
Joseph Zawierucha
Original Assignee
Basf Se
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Application filed by Basf Se filed Critical Basf Se
Publication of WO2010046268A2 publication Critical patent/WO2010046268A2/fr
Publication of WO2010046268A3 publication Critical patent/WO2010046268A3/fr

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles

Definitions

  • the invention relates to a method of controlling Chinese tallowtree and a composition for use in such method.
  • Chinese tallowtree (Sapium sebiferum (L.)), also Triadica sebifera (L.) is an invasive tree species that is native to eastern Asia, e.g. Japan, China and Taiwan, where it is known as a common agricultural weed. Introduced to the U.S. as early as the 1700s, it is found throughout the southern United States, and particularly invades wetland sites where it out-competes native hardwood species. Herbivores and insects have a conditioned behavioral avoidance to eating the leaves of Chinese tallowtree which may at least partly account for the success of the plant as an invasive.
  • herbicides such as glyphosate, triclopyr or imazapyr
  • glyphosate, triclopyr or imazapyr are effective for the control of Chinese tallowtree but will negatively impact the desirable native species when used as a broadcast treatment.
  • herbicides available to control Chinese tallowtree in aquatic and wetland sites are limited. Therefore, there are currently no herbicides that are available for broadcast treatment in wetland sites and will selectively control Chinese tallowtree without damaging or controlling the desirable wetland hardwood species such as oak, baldcypress, and maple.
  • Imazamox is a commercial broad-spectrum herbicide from the class of imidazolinones, and is applied either pre- or post-emergence for control of weeds in maize, rape, alfalfa, peas and beans.
  • WO 2007/071655 discloses the use of imazamox for controlling aquatic weeds.
  • imazamox is suitable for selective control of Chinese tallowtree, in particular in wetlands.
  • a method of controlling Chinese tallowtree comprising the step of applying a herbicidally effective amount of the herbicide imazamox or an agriculturally acceptable salt or derivative thereof to Chinese tallowtree, its seeds or other propagating organs or its habitat.
  • a herbicidal composition for controlling Chinese tallowtree comprising
  • Chonese tallowtree as used herein comprises the plants commonly referred to as Chinese tallowtree, Chinese tallow berry, chicken tree, Florida aspen, popcorn tree, vegetable tallow, and whit wax berry, and scientifically denominated as, inter alia, Sapium sebiferum (L. Roxb.), Croton sebiferum, Excoecaria sebifera, Stillingia sebifera, Triadica sebifera, and Triadica sinensis.
  • Sapium sebiferum L. Roxb.
  • Croton sebiferum Croton sebiferum
  • Excoecaria sebifera Excoecaria sebifera
  • Stillingia sebifera Triadica sebifera
  • Triadica sinensis Triadica sinensis
  • ALS inhibitor from the class of imidazolinone herbicides which is described for example in US 5,334,576 and the Pesticide Manual, 14th ed., British Crop Protection Council 2006.
  • the R-lsomer of imazamox is known from e.g. US 5,972,154 or US 6,339,158 B1.
  • racemic form (R/S form) of imazamox is employed.
  • Another preferred embodiment of the invention comprises the use of one of the optical isomers (the R-enantiomer or S-enantiomer) of imazamox, in particular the R- enantiomer of imazamox.
  • cations are the ions of the alkali metals, preferably of lithium, sodium and potassium, of the alkaline earth metals, preferably of calcium and magnesium, and of the transition metals, preferably of manganese, copper, zinc and iron, furthermore substituted ammonium in which one to four hydrogen atoms are replaced by Ci-C 4 -alkyl, hydroxy-CrC 4 -alklyl, Ci-C 4 -alkoxy- Ci-C 4 -alklyl, hydroxyl-Ci-C 4 -alkoxy-Ci-C 4 -alkyl, phenyl or benzyl, preferably methyl- ammonium, isopropylammonium, dimethylammonium, diisopropylammonium, trimethylammonium, tetramethylammonium, tetraethylammonium, tetrabutylammo- nium, 2-hydroxyethylammonium,
  • imazamox can be employed as an agriculturally acceptable derivative, for example as an amide such as mono- or di-CrC ⁇ - alkylamide or arylamide, as an ester, for example as an allyl ester, propargyl ester, d- Cio-alkyl ester or an alkoxyalkyl ester, and also as a thioester, for example as a CrCi 0 - alkyl thioester.
  • an amide such as mono- or di-CrC ⁇ - alkylamide or arylamide
  • an ester for example as an allyl ester, propargyl ester, d- Cio-alkyl ester or an alkoxyalkyl ester
  • thioester for example as a CrCi 0 - alkyl thioester.
  • Preferred mono- and di-CrC ⁇ -alkylamides are methyl- and the dimethylamide.
  • Preferred arylamides are, for example, the anilidine and the 2-chloroanilide.
  • Preferred alkyl esters are, for example, the methyl, ethyl, propyl, isopropyl, butyl, isobu- tyl, pentyl, mexyl(i-methylhexyl) or isooctyl(2-ethylhexyl)ester.
  • Ci-C 4 -alkoxy-CrC 4 -alkyl esters are the straight-chain or branched CrC 4 - alkoxyethyl esters, for example the methoxyethyl, ethoyethyl or butoxyethyl ester.
  • An example of the straight-chain or branched CrCi O -alkyl thioesters is the ethyl thioester.
  • Imazamox can be used in combination with one or more other herbicide(s) or an agri- culturally acceptable salt or derivative thereof.
  • other herbicide(s) are the herbicides B selected from the following classes b1 ) to b15):
  • lipid biosynthesis inhibitors b2 acetolactate synthase inhibitors (ALS inhibitors); b3) photosynthesis inhibitors; b4) protoporphyrinogen-IX oxidase inhibitors; b5) bleacher herbicides; b6) enolpyruvyl shikimate 3-phosphate synthase inhibitors (EPSP inhibitors); b7) glutamine synthetase inhibitors; b8) 7,8-dihydropteroate synthase inhibitors (DHP inhibitors); b9) mitose inhibitors; b10) inhibitors of the synthesis of long chain fatty acids (VLCFA inhibitors); b11 ) cellulose biosynthesis inhibitors; b12) decoupler herbicides; b13) auxin herbicides; b14) auxin transport inhibitors; b15) other herbicides selected from the group consisting of benzoylprop, flamprop, flamprop-M, bromobutide, chlorflurenol,
  • Preferred herbicides of groups b1 ) to b15) are the compounds listed below:
  • lipid biosynthesis inhibitors from the group of the lipid biosynthesis inhibitors: chlorazifop, clodinafop, clofop, cyhalofop, diclofop, fenoxaprop, fenoxaprop-p, fenthiaprop, fluazifop, fluazifop-P, haloxyfop, haloxyfop-P, isoxapyrifop, metami- fop, propaquizafop, quizalofop, quizalofop-P, trifop, alloxydim, butroxydim, clethodim, cloproxydim, cycloxydim, profoxydim, sethoxydim, tepraloxydim, tralkoxydim, butylae, cycloate, diallate, dimepiperate, EPTC, esprocarb, ethiolate, isopolinate, methiobencarb
  • ALS inhibitors amidosulfuron, azimsulfuron, bensulfuron, chlorimuron, chlorsulfuron, cinosulfu- ron, cyclosulfamuron, ethametsulfuron, ethoxysulfuron, flazasulfuron, flupyrsulfu- ron, foramsulfuron, halosulfuron, imazosulfuron, iodosulfuron, mesosulfuron, metsulfuron, nicosulfuron, oxasulfuron, primisulfuron, prosulfuron, pyrazosulfu- ron, rimsulfuron, sulfometuron, sulfosulfuron, thifensulfuron, triasulfuron, tribenuron, trifloxysulfuron, triflusulfuron, tritosulfuron,
  • b3 from the group of the photosynthesis inhibitors: atraton, atrazine, ametryne, aziprotryne, cyanazine, cyanatryn, chlorazine, cyprazine, desmetryne, dimethametryne, dipropetryn, eglinazine, ipazine, meso- prazine, methometon, methoprotryne, procyazine, proglianzine, prometon, pro- metryne, propazine, sebuthylazne, secbumeton, simazine, simeton, simetryne, terbumeton, terbuthylazine, terbutryne, trietazine, ametridione, amibuzin, hexazi- none, isomethiozin, metamitron, metribuzin, bromacil, isocil, lenacil, terbacil, brompyrazon, chlorida
  • acifluorfen from the group of the protoporphyringogen-IX oxidase inhibitors: acifluorfen, bifenox, chlomethoxyfen, chlornitrofen, ethoxyfen, fluorodifen, fluoro- glycofen, fluoronitrofen, fomesafen, furyloxyfen, halosafen, lactofen, nitrofen, ni- trofluorfen, oxyfluorfen, fluazolate, pyraflufen, cinidon-ethyl, flumiclorac, flumi- oxazin, flumipropyn, fluthiacet, thidiazimin, oxadiazon, oxadiargyl, azafenidin, carfentrazone, sulfentrazone, pentoxazone, benzfendizone, butafenacil, pyraclo- nil, profluazol, flufen
  • 3-en-2-one known from EP 338992, 2-[2-chloro-4-(methylsulfonyl)-3-[(2,2,2- trifluoroethoxy)methyl]-3-hydroxy-3-cyclohexen-1-one (known from DE 19846792), and pyrasulfotole;
  • mitose inhibitors benfluralin, butralin, dinitramine, ethalfluralin, fluchloralin, isopropalin, methalpro- palin, nitralin, oryzalin, pendimethalin, prodiamine, profluralin, trifluralin, amipro- fos-methyl, butamifos, dithiopyr, thiazopyr, propyzamide, tebutam, chlorthal, car- betamide, chlorbufam, chlorpropham and propham;
  • VLCFA inhibitors from the group of the VLCFA inhibitors: acetochlor, alachlor, butachlor, butenachlor, delachlor, diethatyl, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, S-metolachlor, preti- lachlor, propachlor, propisochlor, prynachlor, terbuchlor, thenylchlor, xylachlor, al- lidochlor, CDEA, epronaz, diphenamid, napropamide, naproanilide, pethoxamid, flufenacet, mefenacet, fentrazamide, anilofos, piperophos, cafenstrole, indanofan and tridiphane;
  • b12 from the group of the decoupler herbicides: dinofenate, dinoprop, dinosam, dinoseb, dinoterb, DNOC, etinofen and medinoterb;
  • auxin herbicides clomeprop, 2,4-D, 2,4,5-T, MCPA, MCPA thioethyl, dichlorprop, dichlorprop-P, mecoprop, mecoprop-P, 2,4-DB, MCPB, chloramben, dicamba, 2,3,6-TBA, tri- camba, quinclorac, quinmerac, clopyralid, fluroxypyr, picloram, triclopyr, bena- zolin and aminopyralid;
  • auxin transport inhibitors naptalam, diflufenzopyr
  • herbicides B of groups b1 ) to b15) are known herbicides, see the quoted literature references and, for example, The Compendium of Pesticide Common Names
  • the weight ratio of the active compounds imazamox : B is usually in the range from 1 : 500 to 10 : 1 , preferably in the range from 1 : 100 to 10 : 1 , in particular in the range from 1 : 50 to 10 : 1 and particularly preferably in the range from 1 : 25 to 5 : 1.
  • Imazamox and optionally one or more herbicides B may be present in suspended, emulsified or dissolved form and can be formulated jointly or separately.
  • the application forms depend entirely on the intended use.
  • the preparations can be applied, for example, in the form of directly sprayable aqueous solutions, powders, suspensions, also highly-concentrated aqueous, or other suspensions or dispersions, pastes, dusts, materials for spreading or granules, by means of spraying, atomizing, dusting, broadcasting or watering, depending on the intended application form.
  • the finest possible distribution of the active compounds should be ensured. Coarser distribution might be desired e.g. when a different activity is to be achieved.
  • the preparations comprise one or more liquid or solid carriers, if appropriate surfactants and if appropriate further auxiliaries which are customary for formulating crop protection products.
  • surfactants e.g., sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium bicarbonate, sodium sulfate, sodium bicarbonate
  • Suitable inert additives with carrier function are essentially: oils of vegetable or animal origin, aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahydronaphtha- lene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohexanol, ketones such as cyclohexanone, strongly polar solvents, e.g. amines such as N- methylpyrrolidone, and water.
  • oils of vegetable or animal origin aliphatic, cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahydronaphtha- lene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butan
  • solid carriers examples include mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nut- shell meal, cellulose powders and other solid carriers.
  • mineral earths such as silica gels, silicates, talc, kaolin, attaclay, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nut- shell meal, cellulose powders and other solid carriers.
  • Suitable surfactants include the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, e.g. ligno-, phenol-, naphthalene- and dibutyl- naphthalenesulfonic acid, and of fatty acids, of alkyl- and alkylarylsulfonates, of alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols and of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octyl- phenol ether, ethoxylated
  • Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wettable powders or water-dispersible granules by adding water.
  • the active compound(s) as such or dissolved in an oil or solvent can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier.
  • concentrates consisting of active compound(s), wetting agent, tackifier, dispersant or emulsifier and, if desired, solvent or oil, and these concentrates are suitable for dilution with water.
  • Powders, materials for spreading and dusts can be prepared by mixing or concomitant grinding of the active compounds with a solid carrier.
  • Granules e.g. granules coated by active compound(s), granules impregnated by active compound(s) and granules wherein the active compound(s) are homogenously distributed, can be prepared by binding the active compound(s) to solid carriers.
  • Solid carriers are mineral earths such as silicas, silica gels, silicates, talc, kaolin, limestone, lime, chalk, bole, loess, clay, dolomite, diatomaceous earth, calcium sulfate, magnesium sulfate, magnesium oxide, ground synthetic materials, products of vegetable origin such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders, or other solid carriers.
  • the binding can be achieved e.g. by means of immersion, spraying or extrusion.
  • concentrations of the active ingredient(s) in the ready-to-use preparations can be varied within wide ranges.
  • the formulations comprise from 0.001 to 98% by weight, preferably 0.01 to 95% by weight, of active ingredient(s).
  • the active ingredi- ent(s) are preferably employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • the preparations can, for example, be formulated as follows:
  • 1 20 parts by weight of the active ingredient(s) in question are dissolved in a composition composed of 80 parts by weight of alkylated benzene, 10 parts by weight of the adduct of 8 to 10 mol of ethylene oxide to 1 mol of oleic acid N- monoethanolamide, 5 parts by weight of calcium dodecylbenzenesulfonate and 5 parts by weight of the adduct of 40 mol of ethylene oxide to 1 mol of castor oil.
  • aqueous dispersion which comprises 0.02% by weight of the active ingredient(s).
  • V 3 parts by weight of the active ingredient(s) in question are mixed with 97 parts by weight of finely divided kaolin. This gives a dust which comprises 3% by weight of the active ingredient(s).
  • VI 20 parts by weight of the active ingredient(s) in question are mixed intimately with 2 parts by weight of calcium dodecylbenzenesulfonate, 8 parts by weight of fatty alcohol polyglycol ether, 2 parts by weight of the sodium salt of a phenol-urea- formaldehyde condensate and 68 parts by weight of a paraffinic mineral oil. This gives a stable oily dispersion.
  • VIII 1 part by weight of the active ingredient(s) in question is dissolved in a composition composed of 80 parts by weight of cyclohexanone and 20 parts by weight of nonionic emulsifier based on ethoxylated castor oil (Wettol® EM 31 , BASF AG). This gives a stable emulsion concentrate.
  • the required application rate of imazamox depends on the density of the Chinese tallowtree, on the development stage of the plants, on the climatic conditions of the location where the preparation is used and on the application method. In general, the application rate is from 0.0112 kg/ha to 1 1.2 kg/ha, preferentially from 0.01 12 kg/ha to 1.12 kg/ha, particularly preferred from 0.28 kg/ha to 0.56 kg/ha.
  • the method of the invention is useful for controlling Chinese tallowtree by applying a herbicidally effective amount of imazamox or an agriculturally acceptable salt or derivative thereof - generally in the form of a herbicidal preparation - to the Chinese tallowtree, its seeds or other propagating organs, or its habitat.
  • Foliar spray applications including low volume foliar spray applications, are preferred at all developments stages. Soil application is also preferred, which will also control seeds. In aquatic areas it is also feasible to apply the herbicidal preparation directly to a water body to control plants in or bordering the water body (water application).
  • basal (also basal bark) application frill application, girdling application, spaced out application, cut stump application, as well as tree stem or stump injection application (e.g. by utilizing an EZject ® ) are also preferred.
  • the method of the invention is applicable in all habitats of Chinese tallowtree, including coastal prairies, swamps, marshes, woodlands, alluvial forests and plains, upland well-drained areas, canopy forests, bottomland hardwood forests and shores of water bodies.
  • Aquatic habitat means an area comprising open water bodies or comprising permanently wet soil, where the applied herbicide is likely to come into contact with surface or ground water.
  • Aquatic sites include lakes, ponds, rivers, streams, riparian zones, wetlands and other areas where the soils have seasonal or permanently wet soils. The plants to be controlled in such a habitat either grow in or near an aquatic site.
  • the method of the invention is further suitable for selectively controlling Chinese tallowtree, preferably in the presence of other tree species, in particular hardwood spe- cies, such as oak, like water oak, maple, like red maple, dogwood, like swamp dogwood, willow, like black willow, cypress, like bald cypress, and elderberry.
  • hardwood spe- cies such as oak, like water oak, maple, like red maple, dogwood, like swamp dogwood, willow, like black willow, cypress, like bald cypress, and elderberry.
  • the invention further provides for the use of imazamox and its agrochemically acceptable salts and derivative for controlling Chinese tallowtree, in particular according to one of the preferred embodiments listed above.
  • a small plot of hardwood species containing Chinese tallowtree was treated with ima- zamox (Clearcast ® , commercial SL formulation containing 1 Ib/gal imazamox, available from BASF Corp.).
  • the plot included Chinese tallowtree, water oak (Quercus nigra) and dogwood (Cornus spp.)- Clearcast ® was applied with a handgun application at a 0.5 % volume ratio with 50 gallons of water carrier per acre. Methylated seed oil surfactant at a 1 % volume ratio was included in the mixture.
  • a helicopter aerial application delivering 15 gallons per acre and Clearcast ® at 48 and 64 oz/A plus methylated seed oil was conducted to 2, 5-acre plots containing a mixture of Chinese tallowtree, willow oak, nuttall oak, elm, and bald cypress.
  • One year after application no mortality was documented on the oak, elm and bald cypress.
  • Chinese tallowtree was severely impacted in both 5 acre test plots, with mortality estimated at 75% on trees ranging from 15 - 50' tall.

Abstract

La présente invention concerne l’imazamox en tant qu’herbicide adapté pour le contrôle sélectif de l’arbre à suif même dans des environnements aquatiques.
PCT/EP2009/063303 2008-10-20 2009-10-13 Procédé de contrôle de l'arbre à suif WO2010046268A2 (fr)

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US10687408P 2008-10-20 2008-10-20
US61/106,874 2008-10-20

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WO2010046268A3 WO2010046268A3 (fr) 2011-01-06

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Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103004594A (zh) * 2012-12-13 2013-04-03 中国科学院合肥物质科学研究院 一种通过幼胚胚状体发生途径诱导乌桕植株再生的方法
EP3162209A1 (fr) 2015-10-27 2017-05-03 BASF Agro B.V. Composition herbicide comprenant de cinméthyline et de l'imazamox
US10375959B2 (en) 2015-01-22 2019-08-13 BASF Agro B.V. Ternary herbicidal combination comprising saflufenacil
US10729141B2 (en) * 2013-05-06 2020-08-04 Stephen F. Austin State University Compositions and methods to selectively control invasive species
US10813356B2 (en) 2015-07-10 2020-10-27 BASF Agro B.V. Herbicidal composition comprising cinmethylin and dimethenamid
US10897898B2 (en) 2015-07-10 2021-01-26 BASF Agro B.V. Herbicidal composition comprising cinmethylin and acetochlor or pretilachlor
US10980232B2 (en) 2015-07-10 2021-04-20 BASF Agro B.V. Herbicidal composition comprising cinmethylin and pyroxasulfone
US11116213B2 (en) 2015-07-10 2021-09-14 BASF Agro B.V. Herbicidal composition comprising cinmethylin and pethoxamid
US11206827B2 (en) 2015-07-10 2021-12-28 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids
US11219215B2 (en) 2015-07-10 2022-01-11 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase
US11219212B2 (en) 2015-07-10 2022-01-11 BASF Agro B.V. Herbicidal composition comprising cinmethylin and imazamox
US11291206B2 (en) 2015-07-10 2022-04-05 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors
US11517018B2 (en) 2015-07-10 2022-12-06 BASF Agro B.V. Herbicidal composition comprising cinmethylin and saflufenacil

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
Anonymous: "26th Annual Western Aquatic PlantManagement Society Meeting" WAPMS 25 March 2007 (2007-03-25), page 22PP, XP002604442 Idaho Retrieved from the Internet: URL:http://www.wapms.org/abstracts/2007_WAPMS_program.pdf [retrieved on 2010-10-11] *

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103004594A (zh) * 2012-12-13 2013-04-03 中国科学院合肥物质科学研究院 一种通过幼胚胚状体发生途径诱导乌桕植株再生的方法
US10729141B2 (en) * 2013-05-06 2020-08-04 Stephen F. Austin State University Compositions and methods to selectively control invasive species
US10375959B2 (en) 2015-01-22 2019-08-13 BASF Agro B.V. Ternary herbicidal combination comprising saflufenacil
US10980232B2 (en) 2015-07-10 2021-04-20 BASF Agro B.V. Herbicidal composition comprising cinmethylin and pyroxasulfone
US10813356B2 (en) 2015-07-10 2020-10-27 BASF Agro B.V. Herbicidal composition comprising cinmethylin and dimethenamid
US10897898B2 (en) 2015-07-10 2021-01-26 BASF Agro B.V. Herbicidal composition comprising cinmethylin and acetochlor or pretilachlor
US11116213B2 (en) 2015-07-10 2021-09-14 BASF Agro B.V. Herbicidal composition comprising cinmethylin and pethoxamid
US11206827B2 (en) 2015-07-10 2021-12-28 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific quinolinecarboxylic acids
US11219215B2 (en) 2015-07-10 2022-01-11 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific inhibitors of protoporphyrinogen oxidase
US11219212B2 (en) 2015-07-10 2022-01-11 BASF Agro B.V. Herbicidal composition comprising cinmethylin and imazamox
US11291206B2 (en) 2015-07-10 2022-04-05 BASF Agro B.V. Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors
US11517018B2 (en) 2015-07-10 2022-12-06 BASF Agro B.V. Herbicidal composition comprising cinmethylin and saflufenacil
EP3162209A1 (fr) 2015-10-27 2017-05-03 BASF Agro B.V. Composition herbicide comprenant de cinméthyline et de l'imazamox

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AR075654A1 (es) 2011-04-20

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