WO2020126579A1 - Combinaisons herbicides - Google Patents

Combinaisons herbicides Download PDF

Info

Publication number
WO2020126579A1
WO2020126579A1 PCT/EP2019/084125 EP2019084125W WO2020126579A1 WO 2020126579 A1 WO2020126579 A1 WO 2020126579A1 EP 2019084125 W EP2019084125 W EP 2019084125W WO 2020126579 A1 WO2020126579 A1 WO 2020126579A1
Authority
WO
WIPO (PCT)
Prior art keywords
herbicide
imazamox
herbicides
weight
salt
Prior art date
Application number
PCT/EP2019/084125
Other languages
English (en)
Inventor
Helmut Kraus
Cyrill Zagar
Tobias SEISER
Johannes BESSAI
Tatjana DIMITRIADI
Yannick Griveau
Danielle Reid
Nocha Van Thielen
JDavid PETERS
Jeffrey Brown
Original Assignee
Basf Agrochemical Products B.V.
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Basf Agrochemical Products B.V. filed Critical Basf Agrochemical Products B.V.
Priority to EP19829413.4A priority Critical patent/EP3897138A1/fr
Priority to EA202191587A priority patent/EA202191587A1/ru
Publication of WO2020126579A1 publication Critical patent/WO2020126579A1/fr

Links

Classifications

    • 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
    • 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
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants

Definitions

  • the present invention relates to binary and ternary herbicidal combinations of herbicides A, B, and optionally C, as active ingredients and their use for controlling undesirable vegetation in cultures of crop plants, especially in crops which are tolerant to imidazolinone herbicides.
  • crop protection it is principally desirable to increase the specificity and the reliability of the action of active compounds.
  • crop protection products control the harmful plants effectively and, at the same time, are tolerated by the useful plants in question.
  • Imazamox (lUPAC: 2-[(RS)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-5-methoxy- methylnicotinic acid), as well as its salts and esters, is a well-known broad spectrum herbicide from the group of the imidazolinone herbicides (see C.D.S Tomlin (Ed.), The Pesticide Manual, 14th ed., 2006, BCPC Alton, Hampshire, UK, p. 587 ff.). Imazamox is known to be absorbed by the foliage or roots of the plants and effectively blocks the synthesis of branched chain amino acids by inhibition of acetolactate synthase (ALS inhibitor or AHAS inhibitor).
  • ALS inhibitor or AHAS inhibitor acetolactate synthase
  • Formulations of imazamox comprising the active ingredient as racemate, are marketed under the trade names Beyond®, Raptor® and Sweeper®, Clearfield Vantiga®, Cleranda®, Clearvis® or Cleravo®.
  • Cleravo® is a sus pension concentrate containing 35 g/l imazamox and 250 g/l quinmerac.
  • Intervix® is a water soluble liquid (SL) formulation, which comprises the racemic form of imazamox (33 g/l) and ima- zapyr (15 g/l).
  • Imazapyr (lUPAC: 2-[(RS)-4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]-5-methylnicotinic acid), an imidazolinone herbicide, as well as its salts and esters, is a well-known broad spectrum herbicide from the group of the imidazolinone herbicides (see C.D.S Tomlin (Ed.), The Pesticide Manual, 14th ed., 2006, BCPC Alton, Hampshire, UK, p. 587 ff.). It is frequently used with co herbicides. The herbicidal activity and the activity spectrum, however, is only limited.
  • WO09112454 teaches that co-application of pyroxasulfone and the imidazolinone herbicides imazamox and imazapyr may lead to enhanced herbicidal activity.
  • a synergistic control of Poa, Polygonum and Setaria plants is described in US6,673,748 for mixtures comprising imazamox and pendimethalin.
  • ALS tolerant crops such as, for example, ALS tolerant wheat, ALS tolerant durum, ALS tolerant triticale, ALS tolerant rye and ALS tolerant barley, but also with ALS
  • the combination should in particular be useful for controlling undesirable harmful plants in crops which are toler ant against imidazolinone herbicides, such as the so called Clearfield® crops mentioned above.
  • the combination should have a good pre- to post-emergence herbicidal activity against harmful plants, in particular against annual and perennial grasses and broadleaf weeds, especially against herbicide resistant harmful plants species.
  • the combination should have good compatibility with the subsequent crop plants, which are planted after harvest of the imidazolinone tolerant crops (crop rotation, re-cropping).
  • the herbicide A is R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or an agricul turally acceptable salt or ester thereof;
  • the herbicide B is imazapyr, or an agriculturally acceptable salt or ester thereof; and c. the optional herbicide C is selected from the group consisting of aclonifen, bixlozone, car- fentrazone, clethodim, clomazone, cycloxydim, dimethenamid-P, ethalfluralin, fluazifop, fluazifop-P, halauxifen, haloxyfop, haloxyfop-P, S-metolachlor, pendimethalin, pethox- amide, prohexadione, propaquizafop, propisochlor, prosulfocarb, pyroxasulfone, quizalo- fop, quizalofop-P, sethoxydim, sulfentrazone, terbuthylazine, trifluralin, and the salts and esters thereof.
  • the optional herbicide C is selected from the group
  • the invention furthermore relates to the use of a combination as defined herein for controlling undesirable vegetation in cultures of crop plants, wherein the crop plant is selected from imid azolinone tolerant crops.
  • the invention furthermore relates to the use of a combination as defined herein for controlling undesirable vegetation in cultures of crop plants, wherein the crop plant is selected from imid azolinone tolerant crops, and wherein the undesirable vegetation comprises herbicide resistant harmful plants species.
  • the invention furthermore relates to the use of a combination as defined herein for controlling undesirable vegetation in crops which, by genetic engineering, genome editing or by breeding, are resistant or tolerant to one or more herbicides, in particular against herbicides from the group of inhibitors of acetolactate synthase (ALS inhibitor compounds), such as imidazolinone herbicides, sulfonylurea herbicides or triazolpyrimidine herbicides and/or pathogens, such as harmful fungi, and/or to attack by insects; in particular crops which, by genetic engineering or by breeding, are resistant or tolerant to imidazolinone herbicides, such as imidazolinone resistant wheat, barley, corn, rice, sunflower, lentils, and oilseed rape (canola), preferably sunflower.
  • ALS inhibitor compounds such as imidazolinone herbicides, sulfonylurea herbicides or triazolpyrimidine herbicides and/or pathogens, such as harmful fungi, and/or
  • the invention furthermore relates to a method for controlling undesirable vegetation which com prises applying a herbicidal combination according to the present invention to the undesirable plants, or to the locus, where undesirable vegetation is expected to occur.
  • Application can be done before, during and/or after, preferably during and/or after, in particular after the emergence of the undesirable plants.
  • the herbicide A, the herbicide B, and the optional herbicide C can be applied simultaneously or in succession to the areas, where undesirable vegetation occurs or may occur.
  • the invention in particular, relates to a method for controlling undesirable vegetation in crops which comprises applying an herbicidal composition according to the present invention in crops, where undesirable vegetation occurs or might occur.
  • the invention furthermore, relates to a method for controlling undesirable vegetation which comprises allowing a combination according to the present invention to act on plants, their habi tat or on seed.
  • the invention furthermore, relates to a method for controlling undesirable vegetation in imid- azolinone tolerant crops, which comprises the step of treating the seed of the imidazolinone tolerant crops with a composition according to the present invention.
  • the herbicide A, the herbicide B, and the optional herbicide C are formulated and applied jointly or separately. In the case of separate application, it is of minor importance, in which order the application takes place. It is only necessary, that the herbicide A, the herbicide B, and the optional herbicide C are applied in a time frame that allows simultaneous action of the active ingredients on the plants, preferably within a time-frame of at most 14 days, in particular of at most 7 days.
  • the invention also relates to an herbicide formulation which comprises a herbicidally active combination as defined herein and at least one carrier material, including liquid and/or solid car rier materials.
  • the combinations according to the present invention have better herbicidal activity against harmful plants than would have been expected by the herbicidal activity of the individual compounds.
  • the joint action of the herbicide A, the herbicide B, and the optional herbicide C results in an enhanced activity against harmful plants in the sense of a synergy ef fect (synergism or potentiation), even at low application rates of the herbicide A, the herbicide B, and the optional herbicide C.
  • the combination of the present invention can, based on the individual components, be used at lower application rates to achieve a herbicidal effect comparable to the individual components.
  • the combinations of the present invention provide good pre- and post-emergence herbicidal activity; in particular, the combinations are useful for combating/controlling harmful plants after their emergence (post-emergence).
  • the combinations of the present invention also show good crop compatibility, i.e. their use in crops does not result in increased damage, in particular if the combinations are applied in crops tolerant to inhibitors of acetolactate synthase, especially in crops tolerant to imidazolinone herbicides or in crops with natural tolerance to one or all of herbicides B and C, or in crops with natural tolerance to all of herbicides A, B and C when compared to the individual application of herbicide A, herbicide B or herbicide C or com pared to the application of a combination of herbicides A and B.
  • the combinations also show an accelerated action on harmful plants, i.e. they damage harmful plants more quick ly when compared with application of the individual herbicides A, B or C and also compared to the application of a combination of herbicides A and B.
  • the term "combination” relates both to a composition containing the herbicides A, B, and op tionally C, as active ingredients and also the combined application of the herbicides A, B, and optionally C, which means that the herbicides A, B, and optionally C, are used together for con trolling undesirable vegetation in crops and non-crop areas.
  • the herbicides A, B, and optional ly C can be applied simultaneously or in succession to the areas, where undesirable vegetation occurs or may occur.
  • the herbicides A, B, and optionally C are, in particular, applied in crops, where undesirable vegetation may occur.
  • composition is understood as a physical admixture of the herbicides A, B, and op tionally C, and, optionally, one or more formulation auxiliaries, such as one or more surfactants.
  • composition includes both a combo-formulation, containing a physical admixture of the herbicides A, B, and optionally C, and a ready to use composition, such as an aqueous spray liquor, obtained by tank mixing solo- or combo-formulations of the herbicides A, B, and optionally C.
  • formulation includes both formulations, containing a physical admixture of the herbi cides A, B, and optionally C, as well as kits-of-parts formulations, where the herbicides A, B, and optionally C, are formulated separately, i.e. as solo formulations or as a kit-of part formula tion, comprising a combo-formulation of the herbicide A and the herbicide B and a solo- formulation of the herbicide C or as a kit-of part formulation, comprising a solo-formulation of the herbicide A and a combo-formulation of the herbicide B and the herbicide C.
  • Both solo- and combo-formulations generally contain at least one formulation auxiliary, such as one or more surfactants, and at least one liquid or solid carrier.
  • the combinations of the invention contain the herbicide A, which is R-imazamox (A-1), any non- racemic mixture of R-imazamox and S-imazamox, wherein the proportion of R-imazamox is at least 80% by weight (A-2), preferably at least 90%, more preferably at least 95%, or an agricul turally acceptable salt or ester thereof.
  • A-1 herbicide A
  • A-2 any non- racemic mixture of R-imazamox and S-imazamox
  • the proportion of R-imazamox is at least 80% by weight (A-2), preferably at least 90%, more preferably at least 95%, or an agricul turally acceptable salt or ester thereof.
  • the combination may comprise R-imazamox (A-1) or any non- racemic mixture of R-imazamox and S-imazamox, wherein the proportion of R-imazamox is at least 80% by weight (A-2), as such or as a salt of R-imazamox (A-3) or any non-racemic mixture of R-imazamox and S-imazamox, wherein the proportion of R-imazamox is at least 80% by weight (A-4), in particular an alkalimetal salt or an ammonium salt or substituted ammonium salt as defined below.
  • the carboxyl group of imazamox may also be present in esterified form, e.g. in the form of a Ci-Cs-alkoxycarbonyl group or in the form of a Ci-C 4 -alkoxy-CrC 4 - alkoxycarbonyl group.
  • esters are the methyl, ethyl, propyl, isopropyl, butyl, isobu tyl, pentyl, mexyl (1-methylhexyl) or isooctyl (2-ethylhexyl) esters.
  • Ci-C4-alkoxy-Cr C4-alkyl esters are the straight-chain or branched CrC4-alkoxyethyl esters, for example the methoxyethyl, ethoxyethyl or butoxyethyl (butoyl) esters.
  • the combinations of the inven tion contain R-imazamox or any non-racemic mixture of R-imazamox and S-imazamox, wherein the proportion of R-imazamox is at least 80% by weight, as such or as a salt of R-imazamox or any non-racemic mixture of R-imazamox and S-imazamox, wherein the proportion of R- imazamox is at least 80% by weight, in particular an alkalimetal salt or an ammonium salt as defined below.
  • Suitable salts of A-1 and A-2 include the alkali metal salts, preferably the lithium, sodium and potassium salts, the alkaline earth metals salts, e.g. the calcium and magnesium salts, and the transition metal salts, e.g.
  • the manganese, copper, zinc and iron salts furthermore ammonium and substituted ammonium salts (hereinafter also termed as organoammonium salts), in which one to four hydrogen atoms of ammonium are replaced by CrCs-alkyl, CrC4-alkyl, hydroxy-Cr C4-alkyl, in particular hydroxy-C2-C4-alkyl, Ci-C4-alkoxy-CrC4-alkyl, in particular CrC4-alkoxy- C2-C4-alkyl, hydroxy-Ci-C4-alkoxy-Ci-C4-alkyl, in particular hydroxy-C2-C4-alkoxy-C2-C4-alkyl, phenyl or benzyl, preferably ammonium, methylammonium, isopropylammonium, dime- thylammonium, diisopropylammonium, trimethylammonium, tetramethylammonium, tetrae
  • the combinations of the invention contain the herbicide B, which is imazapyr (lUPAC: 2-[(RS)- 4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl]nicotinic acid), i.e. rac- imazapyr, or an agricultural ly acceptable salt or ester thereof.
  • the combination may comprise imazapyr as such (B-1) or as a salt (B-2), in particular an alkalimetal salt or an ammonium salt or substituted am monium salt as defined above for the herbicide A.
  • the combinations of the invention contain imazapyr as such or as a salt thereof, for example as an alkalimetal, ammonium or iso- propylammonium salt.
  • the relative weight ratio of the herbicide A, calcu lated as free acid of imazamox, to the herbicide B, calculated as free acid of imazapyr is in the range from 100: 1 to 1 :20, in particular from 40:1 to 1 :4, especially from 20: 1 to 1 :2.
  • the relative weight ratio is in the range from 5: 1 to 1 :1.
  • the relative weight ratio is in the range from 5:1 to 1 :2; in another particular embodiment, the relative weight ratio is in the range from 3: 1 to 1 :2; in a further par ticular embodiment, the relative weight ratio is in the range from 2: 1 to 1 :2; in a further particular embodiment, the relative weight ratio is in the range from 3: 1 to 1 :1. Accordingly, in the meth ods and uses of the invention, the herbicides A and B are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicides A and B within these weight ratios.
  • the combinations of the present invention may contain a third herbicide C, which is selected from the group consisting of aclonifen, bixlozone, carfentrazone, clethodim, clomazone, cy- cloxydim, dimethenamid-P, ethalfluralin, fluazifop, fluazifop-P, halauxifen, haloxyfop, haloxyfop- P, S-metolachlor, pendimethalin, pethoxamide, prohexadione, propaquizafop, propisochlor, prosulfocarb, pyroxasulfone, quizalofop, quizalofop-P, sethoxydim, sulfentrazone, ter- buthylazine, trifluralin, and the salts and esters thereof.
  • a third herbicide C which is selected from the group consisting of aclonifen,
  • the relative weight ratio of the herbicide A to the herbicide C-1 is preferably in the range from 1 :2000 to 1 :2, in particular from 1 : 1000 to 1 :10, especially from 1 :250 to 1 :25, wherein the herbicide A is calculated as the free acid form of ima- zamox and wherein the herbicide compound C-1 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-1 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-1 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-2 is preferably in the range from 1 : 100 to 2: 1 , in particular from 1 :50 to 1 : 1 , espe cially from 1 : 15 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-2 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-2 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-2 within these weight ratios.
  • lUPAC lUPAC: (RS)-2-chloro-3-(2-chloro-5-[4-(difluoromethyl)-4,5-dihydro-3-methyl-5-oxo-1 /-/- 1 ,2,4-triazol-1-yl]-4-fluorophenyl)propionic acid.
  • exemplary agriculturally acceptable salts or esters of carfentrazone include carfentrazone-ethyl.
  • the relative weight ratio of the herbicide A to the herbicide C-3 is preferably in the range from 1 :50 to 4: 1 , in particular from 1 :20 to 2: 1 , especial ly from 1 :5 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-3 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-3 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-3 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-4 is preferably in the range from 1 : 100 to 2: 1 , in particular from 1 :50 to 1 : 1 , espe cially from 1 : 15 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-4 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-4 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-4 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-5 is preferably in the range from 1 :100 to 2:1 , in particular from 1 :50 to 1 :1 , espe cially from 1 :15 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-5 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-5 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-5 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-6 is preferably in the range from 1 :200 to 2:1 , in particular from 1 :80 to 1 :1 , espe cially from 1 :80 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-6 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-6 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-6 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-7 is preferably in the range from 1 :200 to 2:1 , in particular from 1 :100 to 1 :1 , espe cially from 1 :100 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-7 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-7 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-7 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-8 is preferably in the range from 1 :200 to 2:1 , in particular from 1 :100 to 1 :1 , espe cially from 1 :100 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-8 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-8 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-8 within these weight ratios.
  • CAS 2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid.
  • exemplary agriculturally acceptable salts or esters of fluazifop include fluazifop-butyl.
  • the relative weight ratio of the herbicide A to the herbicide C-9 is preferably in the range from 1 :100 to 2:1 , in particular from 1 :50 to 1 :1 , espe cially from 1 :20 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-9 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-9 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-9 within these weight ratios.
  • CAS (2R)-2-[4-[[5-(trifluoromethyl)-2-pyridinyl]oxy]phenoxy]propanoic acid.
  • exemplary agricul turally acceptable salts or esters of fluazifop-P include fluazifop-P-butyl.
  • the relative weight ratio of the herbicide A to the herbicide C-10 is preferably in the range from 1 :100 to 2:1 , in particular from 1 :50 to 1 :1 , espe cially from 1 :20 to 1 :2, wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-10 is calculated as the free acid.
  • the herbicide A and the herbicide C-10 are preferably ap plied within these weight ratios.
  • the compositions and formulations of the invention contain the herbicide A and the herbicide C-10 within these weight ratios.
  • CAS 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-2-pyridinecarboxylic acid.
  • Exem plary agriculturally acceptable salts or esters of halauxifen include halauxifen-methyl.
  • the relative weight ratio of the herbicide A to the herbicide C-11 is preferably in the range from 100:1 to 1 :5, in particular from 40:1 to 1 :2, espe cially from 10:1 to 1 :1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-11 is calculated as the free acid.
  • the herbicide A and the herbicide C-1 1 are preferably ap plied within these weight ratios.
  • the compositions and formulations of the invention contain the herbicide A and the herbicide C-1 1 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-12 is preferably in the range from 1 :50 to 5: 1 , in particular from 1 :25 to 2: 1 , espe cially from 1 : 10 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-12 is calculated as the free acid.
  • the herbicide A and the herbicide C-12 are preferably ap plied within these weight ratios.
  • the compositions and formulations of the invention contain the herbicide A and the herbicide C-12 within these weight ratios.
  • Exemplary agriculturally acceptable salts or esters of haloxyfop-P include haloxyfop-P-methyl.
  • the relative weight ratio of the herbicide A to the herbicide C-13 is preferably in the range from 1 :50 to 5: 1 , in particular from 1 :25 to 2: 1 , espe cially from 1 : 10 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-13 is calculated as the free acid.
  • the herbicide A and the herbicide C-13 are preferably ap plied within these weight ratios.
  • the compositions and formulations of the invention contain the herbicide A and the herbicide C-13 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-14 is preferably in the range from 1 :2000 to 1 : 1 , in particular from 1 :800 to 1 :2, es pecially from 1 :200 to 1 : 10, wherein the herbicide A is calculated as the free acid form of ima zamox and wherein the herbicide compound C-14 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-14 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-14 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-15 is preferably in the range from 1 :5000 to 1 :2, in particular from 1 :2000 to 1 :5, especially from 1 :500 to 1 :10, wherein the herbicide A is calculated as the free acid form of ima- zamox and wherein the herbicide compound C-15 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-15 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-15 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-16 is preferably in the range from 1 :1000 to 1 :2, in particular from 1 :400 to 1 :4, es pecially from 1 :200 to 1 :10, wherein the herbicide A is calculated as the free acid form of ima- zamox and wherein the herbicide compound C-16 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-16 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-16 within these weight ratios.
  • CAS 3,5-dioxo-4-(1-oxopropyl)cyclohexanecarboxylic acid.
  • exemplary agriculturally acceptable salts or esters of prohexadione include prohexadione-calcium.
  • the relative weight ratio of the herbicide A to the herbicide C-17 is preferably in the range from 1 : 1000 to 1 : 1 , in particular from 1 :200 to 1 : 1 , es pecially from 1 :100 to 1 :2, wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-17 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-17 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-17 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-18 is preferably in the range from 1 :100 to 2:1 , in particular from 1 :50 to 1 :1 , espe cially from 1 :10 to 1 :1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-18 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-18 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-18 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-19 is preferably in the range from 1 :1000 to 1 :2, in particular from 1 :400 to 1 :4, es pecially from 1 :200 to 1 :10, wherein the herbicide A is calculated as the free acid form of ima- zamox and wherein the herbicide compound C-19 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-19 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-19 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-20 is preferably in the range from 1 :5000 to 1 :2, in particular from 1 :2000 to 1 :4, especially from 1 :400 to 1 :10, wherein the herbicide A is calculated as the free acid form of ima- zamox and wherein the herbicide compound C-20 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-20 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-20 within these weight ratios.
  • lUPAC 3-[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1/-/-pyrazol-4-ylmethylsulfonyl]-4,5- dihydro-5, 5-dimethyl-1 ,2-oxazole.
  • the relative weight ratio of the herbicide A to the herbicide C-21 is preferably in the range from 1 :200 to 4:1 , in particular from 1 :50 to 2:1 , espe cially from 1 : 10 to 1 :1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-21 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-21 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-21 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-22 is preferably in the range from 1 :200 to 4: 1 , in particular from 1 :100 to 2: 1 , es pecially from 1 :40 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-22 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-22 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-22 within these weight ratios.
  • lUPAC (R)-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionic acid.
  • exemplary agriculturally acceptable salts or esters of quizalofop-P include quizalofop-P-ethyl and quizalofop-P-tefuryl.
  • the relative weight ratio of the herbicide A to the herbicide C-23 is preferably in the range from 1 :200 to 4: 1 , in particular from 1 :100 to 2: 1 , es pecially from 1 :40 to 1 :1 , wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-23 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-23 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-23 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-24 is preferably in the range from 1 :200 to 20:1 , in particular from 1 :80 to 5: 1 , es pecially from 1 :40 to 2:1 , wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-24 is calculated as such. Accordingly, in the meth ods and uses of the invention, the herbicide A and the herbicide C-24 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-24 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-25 is preferably in the range from 1 :200 to 4: 1 , in particular from 1 :100 to 2: 1 , es pecially from 1 :40 to 1 :1 , wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-25 is calculated as such. Accordingly, in the meth ods and uses of the invention, the herbicide A and the herbicide C-25 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-25 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-26 is preferably in the range from 1 :900 to 1 :1 , in particular from 1 :300 to 1 :1 , es pecially from 1 :80 to 1 :2, wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-26 is calculated as such. Accordingly, in the meth ods and uses of the invention, the herbicide A and the herbicide C-26 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-26 within these weight ratios.
  • the relative weight ratio of the herbicide A to the herbicide C-27 is preferably in the range from 1 :500 to 1 :1 , in particular from 1 :200 to 1 :2, es pecially from 1 :100 to 1 :4, wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-27 is calculated as such. Accordingly, in the meth ods and uses of the invention, the herbicide A and the herbicide C-27 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-27 within these weight ratios.
  • the relative weight ratio of the herbicide A to the total amount of the herbicide B and the herbicide C is preferably from 1 :400 to 5:1 , in particular from 1 :200 to 3:1 , especially 1 :100 to 2:1 , wherein the herbicide A is calculated as the free acid, B is calculated as the free acid, and the herbicide C is calculated as the free acid or as such. Accordingly, in the methods and uses of the invention, the herbicides A, B and C are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicides A, B and C within these weight ratios.
  • Combination 1 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof; Herbicide B: imazapyr or a salt thereof;
  • Herbicide C -
  • Combination 2 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C aclonifen.
  • Combination 3 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C bixlozone.
  • Combination 4 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C carfentrazone or an ester thereof.
  • Combination 5 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C clethodim.
  • Combination 6 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C clomazone.
  • Combination 7 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C dimethenamid-P.
  • Combination 9 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C ethalfluralin.
  • Combination 10 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C fluazifop or an ester thereof.
  • Combination 11 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C fluazifop-P or an ester thereof.
  • Combination 12 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C halauxifen or an ester thereof.
  • Combination 13 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C haloxyfop or an ester thereof.
  • Combination 14 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C haloxyfop-P or an ester thereof.
  • Combination 15 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C S-metolachlor.
  • Combination 16 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C pendimethalin.
  • Combination 17 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C pethoxamid.
  • Combination 18 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C prohexadione or a salt thereof, e.g. prohexadione-calcium.
  • Combination 19 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C propaquizafop.
  • Combination 20 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C propisochlor.
  • Combination 21 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C prosulfocarb.
  • Combination 22 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C pyroxasulfone.
  • Combination 23 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C quizalofop or an ester thereof.
  • Combination 24 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C quizalofop-P or an ester thereof.
  • Combination 25 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C sethoxydim.
  • Combination 26 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C sulfentrazone.
  • Combination 27 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof; Herbicide B: imazapyr or a salt thereof;
  • Herbicide C terbuthylazine.
  • Combination 28 Herbicide A: R-imazamox, any non-racemic mixture of R-imazamox and S- imazamox, wherein the proportion of R-imazamox is at least 80% by weight, or a salt thereof;
  • Herbicide B imazapyr or a salt thereof
  • Herbicide C trifluralin.
  • the weight ratio of herbicide A to herbicide B as well as the weight ratio of herbicide A to herbicide C and the weight ratio of herbicide A to the total amount of herbicides B and C is as defined above.
  • compositions and methods of the present invention are useful for controlling a large variety of harmful plants (undesired vegetation), including monocotyledonous weeds and dicotyle donous weeds, in particular, for controlling weeds, which are selected from the genera Abutilon, Alisma, Alopecurus, Amaranthus, Ambrosia, Ammania, Ammi, Aneilema, Anthemis, Apera, Atri- plex, Avena, Barbarea, Bidens, Brassica, Bromus, Bunias, Butomus, Capsella, Centaurea, Chenopodium, Cirsium, Conium, Convolvolus, Cyperus, Datura, Daucus, Descurainia, Digitaria, Echinochloa, Fumaria, Galinsoga, Galium, Geranium, Helianthus, Heliotropium, Heteranthera, Hibiscus, Hordeum, Lamium, Leptochloa, Leersia, Lolium, Lycops
  • compositions and methods of the present invention are suit able for controlling monocotyledonous weeds, in particular for controlling monocotyledonous weeds, which are selected from the families Poaceae (Gramineae), commonly known as grass es and Cyperaceae, commonly known as sedges.
  • Gramae commonly known as grass es
  • Cyperaceae commonly known as sedges.
  • compositions and methods of the present invention are suitable for controlling monocotyledonous weeds, which are selected from the genera Alo pecurus, Avena, Cyperus, Digitaria, Echinochloa, Leersia, Leptochloa, Lolium, Oryza, Panicum, Poa, Scirpus, Setaria, Sorgum and Triticum, in particular from the species Alopecurus myosu- roides (ALOMY), Avena fatua (AVEFA), Cyperus difformis (CYPDI), Cyperus eragrostis
  • CYPER Cyperus microiria
  • CYPSE Cyperus serotinus
  • Digitaria sanguinalis DIG- SA
  • Echinochloa crus-galli Echinochloa oryzoides
  • EHCG Echinochloa oryzoides
  • LEROR Leersia oryzoides
  • Leptochloa fusca ssp. fascicularis Leptochloa fusca ssp. uninervia
  • LEFUN Lolium multiflorum
  • LLOLMU Lolium multiflorum
  • LRI Lolium rigidum
  • ORY- LO Oryza punctate
  • ORYPU Oryza sativa (Weed Rice and Volunteers)
  • ORYSA Panicum dichotomiflorum
  • PANMI Panicum miliaceum
  • POAAN Panicum miliaceum
  • POAAN Panicum miliaceum
  • POAAN Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • POAAN Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Panicum miliaceum
  • PANMI Pan
  • compositions and methods of the present in vention are suitable for controlling monocotyledonous weeds, which are selected from the gene ra Cyperus, Digitaria, Echinochloa, Leptochloa, Lolium, Oryza, Panicum, Scirpus, Setaria, Sor- gum and Triticum, in particular from the species Cyperus difformis (CYPDI), Cyperus eragrostis (CYPER), Cyperus serotinus (CYPSE), Digitaria sanguinalis (DIGSA), Echinochloa crus-galli (ECHCG), Echinochloa oryzoides (ECHOR), Leptochloa fusca ssp.
  • CYPDI Cyperus difformis
  • CYPER Cyperus eragrostis
  • CYPSE Cyperus serotinus
  • DIGSA Digitaria sanguinalis
  • LEFA Lepto chloa fusca ssp. uninervia
  • LLOLMU Lolium multiflorum
  • ORY- LO Oryza longistaminata
  • Panicum dichotomiflorum PANMI
  • Panicum miliaceum PANMI
  • Poa annua POAAN
  • Scirpus maritimus SCPMA
  • Setaria viridis SETVI
  • Sorghum halepense SORHA
  • TRZAS Triti cum aestivum
  • compositions and methods of the present invention are suitable for controlling dicotyledonous weeds, commonly known as broadleaf weeds
  • compositions and methods of the present in vention are suitable for controlling dicotyledonous weeds from the genera Abutilon, Alisma, Am- aranthus, Ambrosia, Ammannia, Ammi, Anneilema, Atriplex, Bidens, Butomus, Brassica, Che- nopodium, Cirsium, Convolvulus, Datura, Fumaria, Galinsoga, Helianthus, Heliotropium, Heter- anthera, Hibiscus, Matricaria, Orobanche, Polygonum, Portulaca, Solanum, Sonchus, Stachys, Stellaria, and Xanthium, and in particular from the species Abutilon theophrasti (ABUTH), Alis ma lanceolatum (ALSLA), Alisma plantago-aquatica (ALSPA), Amaranthus blitoides (AMABL), Amaranthus retroflexus (AMARE), Ambrosia artemisiifolia (ABUTH), Alis ma lance
  • ORASS Polygonum amphibium
  • POLAM Polygonum amphibium
  • POLAV Polygonum aviculare
  • POLCO Polygonum convolus
  • POLHY Polygonum hydropiper
  • POLLA Polygonum lapathifolium
  • SOLNI Solanum nigrum
  • SONAR Sonchus arvensis
  • STAAN Stachys annua
  • STME Stellaria media
  • XANSI Xanthium orientale ssp. italicum
  • XANSP Xanthium spi- nosum
  • XANST Xanthium strumarium
  • compositions and methods of the present in vention are suitable for controlling dicotyledonous weeds from the genera Abutilon, Alisma, Am- aranthus, Ambrosia, Ammannia, Ammi, Anneilema, Bidens, Butomus, Chenopodium, Cirsium, Convolvulus, Heteranthera, Orobanche, Polygonum, Portulaca, Solanum, Sonchus, and in par ticular from the species Abutilon theophrasti (ABUTH), Alisma lanceolatum (ALSLA), Alisma plantago-aquatica (ALSPA), Amaranthus retroflexus (AMARE), Ambrosia artemisiifolia (AM- BEL), Ammannia coccinea (AMMCO), Ammi majus (AMIMA), Aneilema keisak (ANEKE),
  • ABUTH Abutilon theophrasti
  • ALSLA Alisma lanceolatum
  • Bidens cernua BIDCE
  • Bidens frondosa BIDFR
  • Butomus umbellatus BUTUM
  • Chenopodi um album CHEAL
  • Cirsium arvense CIRAR
  • Convolvulus arvensis CONAR
  • Heteranthera limosa HETLI
  • Heteranthera reniformis HETRE Orobanche sp.
  • ORASS Polygonum hy dropiper
  • POLLA Polygonum lapathifolium
  • SOLNI Solanum nigrum
  • Sonchus arvensis SONAR
  • compositions and methods of the present invention are suitable for controlling monocotyledonous and dicotyledonous weeds in sunflower, wherein the weeds are selected from the genera Abutilon, Alopecurus, Amaranthus, Ambrosia, Ammi, Atri- plex, Avena, Brassica, Chenopodium, Cirsium, Convolvulus, Datura, Digitaria, Echinochloa, Fumaria, Galinsoga, Helianthus, Heliotropium, Hibiscus, Lolium, Matricaria, Orobanche, Pani- cum, Poa, Polygonum, Portulaca, Setaria, Solanum, Sonchus, Stachys, Stellaria, and Xanthi- um; and in particular from the species Abutilon theophrasti (ABUTH), Amaranthus retroflexus (AMARE), Ambrosia artemisiifolia (AMBEL), Ammi majus (AMIMA), Chenopodium album (CHEAL
  • ORASS Panicum miliaceum
  • PANMI Panicum miliaceum
  • POROL Portulaca oleracea
  • SETVI Setaria viridis
  • SOLNI Solanum nigrum
  • compositions and methods of the present in vention are suitable for controlling monocotyledonous weeds in sunflower, which are selected from the genera Digitaria, Echinochloa, Lolium, Panicum, and Setaria; in particular from the species Digitaria sanguinalis (DIGSA), Echinochloa crus-galli (ECHCG), Lolium multiflorum (LOLMU), Panicum miliaceum (PANMI), and Setaria viridis (SETVI).
  • DIGSA Digitaria sanguinalis
  • EHCG Echinochloa crus-galli
  • LLOLMU Lolium multiflorum
  • PANMI Panicum miliaceum
  • Setaria viridis Setaria viridis
  • compositions and methods of the present invention are suitable for controlling dicotyledonous weeds in sunflower, which are selected from the genera Abutilon, Amaranthus, Ambrosia, Ammi, Chenopodium, Cirsium, Convolvulus, Orobanche, Portulaca, Solanum, Sonchus; and in particular from the species Abutilon the ophrasti (ABUTH), Amaranthus retroflexus (AMARE), Ambrosia artemisiifolia (AMBEL), Ammi majus (AMIMA), Chenopodium album (CHEAL), Cirsium arvense (CIRAR), Convolvulus arven- sis (CONAR), Orobanche sp. (ORASS), Portulaca oleracea (POROL), Solanum nigrum
  • compositions and methods of the present invention are suitable for controlling undesirable vegetation, wherein the undesirable vegetation comprises volunteer crop plants.
  • Volunteer crop plants are crop plants that volunteer in planted crops.
  • compositions and methods of the pre sent invention are suitable for controlling undesirable vegetation, wherein the undesirable vege tation comprises volunteer crop plants selected from the genera Brassica, Hordeum, and Triti- cum, in particular from the species Brassica napus (BRSNW, BRSNS) Hordeum vulgare (HORVW, HORVS), Triticum aestivum (TRZAW, TRZAS), Triticum durum (TRZDU).
  • the undesirable vege tation comprises volunteer crop plants selected from the genera Brassica napus (BRSNW, BRSNS) Hordeum vulgare (HORVW, HORVS), Triticum aestivum (TRZAW, TRZAS), Triticum durum (TRZDU).
  • compositions and methods of the present invention are useful for controlling monocotyledonous and dicotyledonous species, which are herbicide re sistant or tolerant.
  • Exemplary herbicide resistant or tolerant weed species include, but are not limited to, biotypes resistant or tolerant to herbicides selected from the group consisting of acetyl CoA carboxylase (ACCase) inhibitors (HRAC Group A), acetolactate synthase (ALS) inhibitors (HRAC Group B), photosystem II (PS II) inhibitors (HRAC Groups C1 , C2 and C3), photosystem I (PS I) inhibitors (HRAC Group D), protoporphyrinogen oxidase (PPO) inhibitors (HRAC Group E), 4- hydroxyphenyl-pyruvate-dioxygenase (HPPD) inhibitors (HRAC Group F1), phytoene desatu- rase (PDS) inhibitors (HRAC Group F2), carotenoid biosynthesis inhibitors (HRAC Group F3), DOXP synthase inhibitors (HRAC Group F4), 5- enolpymvylshikimate-3-phosphate (EPSP) in hibi
  • the herbicide resistant or tolerant weed species is selected from biotypes resistant or tolerant to herbicides selected from the group consisting of acetyl CoA carboxylase (ACCase) inhibitors (HRAC Group A), acetolactate synthase (ALS) inhibitors (HRAC Group B), photosystem II (PS II) inhibitors (HRAC Groups C1 , C2 and C3), protoporphyrinogen oxidase (PPO) inhibitors (HRAC Group E), 4-hydroxyphenyl-pyruvate-dioxygenase (HPPD) inhibitors (HRAC Group F1), phytoene desaturase (PDS) inhibitors (HRAC Group F2), 5- enolpymvylshikimate-3-phosphate (EPSP) inhibitors (HRAC Group G), inhibitors of microtubuli assembly (HRAC Group K1), very long chain fatty acid (VLCFA) inhibitors (HRAC Group K3), Inhibitors of cell wall synthesis (HRAC Group A
  • the herbicide resistant or tolerant weed species is selected from biotypes resistant or tolerant to herbicides selected from the group consisting of acetyl CoA carboxylase (ACCase) inhibitors (HRAC Group A), acetolactate synthase (ALS) inhibitors (HRAC Group B), photosystem II (PS II) inhibitors (HRAC Groups C1 , C2 and C3), inhibitors of microtubuli assembly (HRAC Group K1), very long chain fatty acid (VLCFA) inhibitors (HRAC Group K3) and inhibitors of lipid synthesis (HRAC Group N).
  • ACCase acetyl CoA carboxylase
  • ALS acetolactate synthase
  • PS II photosystem II
  • HRAC Groups C1 , C2 and C3 inhibitors of microtubuli assembly
  • VLCFA very long chain fatty acid
  • HRAC Group N inhibitors of lipid synthesis
  • the herbicide resistant or tolerant weed species is selected from biotypes with resistance or tolerance to at least one herbicide selected from the group consisting of acetyl CoA carboxylase (ACCase) inhibitors (HRAC Group A), acetolactate synthase (ALS) inhibitors (HRAC Group B) and photosystem II (PS II) inhibitors (HRAC Groups C1 , C2 and C3).
  • ACCase acetyl CoA carboxylase
  • ALS acetolactate synthase
  • PS II photosystem II
  • the resistant or tolerant biotype is selected from the genera Agropyron, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cynodon, Digitaria, Echinochloa, Eleusine, Is- chaemum, Leptochloa, Lolium, Panicum, Phalaris, Poa, Rottboellia, Setaria, Sorghum, Abutilon, Anthemis, Amaranthus, Ambrosia, Capsella, Centaurea, Chenopodium, Descurainia, Erigeron, Galium, Geranium, Kochia, Matricaria, Papaver, Polygonum, Raphanus, Sinapis, Sisymbrium, Stellaria and Thlaspi.
  • the resistant or tolerant biotype is selected from the genera Agropyron,
  • Alopecurus Alopecurus, Avena, Brachiaria, Bromus, Digitaria, Echinochloa, Eleusine, Leptochloa, Lolium, Panicum, Phalaris, Poa, Setaria, Sorghum, Abutilon, Amaranthus, Ambrosia, Chenopodium, Erigeron, Kochia, Matricaria, Papaver, Polygonum, Raphanus, Sinapis, and Stellaria.
  • the resistant or tolerant biotype is selected from the genera
  • the resistant or tolerant biotype is selected from the genera Alopecurus, Apera, Digitaria, Echinochloa, Leptochloa, Phalaris, Poa, Setaria, Amaranthus, Anthemis, Capsella, Centaurea, Chenopodium, Descurania, Kochia, Matricaria, Papaver, Sisymbrium, Stellaria and Thlaspi, more preferably selected from the genera Alopecurus, Apera, Echi grandsloa, Leptochloa, Phalaris, Poa, Amaranthus, Chenopodium, Matricaria, Papaver and Stel laria, even more preferably selected from the genera Alopecurus, Echinochloa, Phalaris, Poa, Amaranthus, Chenopodium, Matricaria, Papaver and Stellaria, yet more preferably selected from the genera Alopecurus, Echinochloa, Phalaris, Poa and Papaver and in particular selected from the genera Alopecurus,
  • the resistant or tolerant biotype is selected from the genera Avena, Echinochloa, Lolium, Setaria, Sorghum, Abutilon, Amaranthus, Anthemis, Chenopodium, Gali um, Geranium, Polygonum and Stellaria.
  • the combinations of the present invention are suitable for combating/controlling undesired veg etation in legumes, such as beans, peas, soy beans or in ALS tolerant crops, in particular in ALS tolerant small-grain cereal crops, such as, for example, ALS tolerant wheat, ALS tolerant durum, ALS tolerant triticale, ALS tolerant rye and ALS tolerant barley, but also in ALS tolerant corn, ALS tolerant sugar beet, ALS tolerant potato, ALS tolerant rice, ALS tolerant sunflower and ALS tolerant oilseed rape (canola).
  • the combinations of the present invention are particu larly suitable for combating/controlling undesired vegetation in ALS tolerant sunflower, canola, lentils, wheat and barley, preferably in ALS tolerant sunflower.
  • the combinations of the invention are particularly useful in crops that are tolerant against imid- azolinone herbicides, such as Clearfield® crops, e.g. Clearfield® canola, Clearfield® rice, Clear field® corn, Clearfield® wheat, Clearfield® Sunflower, Clearfield Lentils, Clearfield Corn, and Cultivance® crops, in particular in Clearfield® Sunflower.
  • Clearfield® crops e.g. Clearfield® canola, Clearfield® rice, Clear field® corn, Clearfield® wheat, Clearfield® Sunflower, Clearfield Lentils, Clearfield Corn, and Cultivance® crops, in particular in Clearfield® Sunflower.
  • the combinations of the invention are particularly useful for combating/controlling undesired vegetation in in the following crops:
  • a Sunflower containing the CL CLHA Plus AHASL trait having an A122(Af)T substi tution or two substitutions, an A122(Af)T substitution and an A205 (Af)V substitution.
  • b Sunflower containing the CL ImiSun AHASL trait having an A205 (Af)V substitu tion.
  • c Sunflower containing both the CL CLHA Plus or CL ImiSun trait and one or two additional AHASL trait(s) that each have substitution(s) at at least one of the posi tions A122(Af), P197(Af), R199(Af), T203(Af), A205 (At), W574(Af), S653 (At), or G654(Af).
  • the combinations of the invention are suitable for application in any vari ety of the aforementioned crop plants.
  • the combinations according to the invention can also be used in crop plants that have been modified by breeding, mutagenesis or genetic engineering, e.g. have been rendered tolerant to applications of specific classes of herbicides, such as imidazolinone herbicides, such as ima- zamox, auxinic herbicides, such as dicamba or 2,4-D; bleacher herbicides, such as 4- hydroxyphenylpyruvate dioxygenase (HPPD) inhibitors or phytoene desaturase (PDS) inhibi tors; acetolactate synthase (ALS) inhibitors, such as sulfonylureas or imidazolinones; enolpy- ruvyl shikimate 3-phosphate synthase (EPSP) inhibitors, such as glyphosate; glutamine synthe tase (GS) inhibitors, such as glufosinate; protoporphyrinogen-IX oxidase inhibitors; lipid bio
  • e. bromoxynil or ioxynil herbicides as a result of conventional methods of breeding or genetic engineering; furthermore, plants have been made resistant to multiple classes of herbicides through multiple genetic modifications, such as resistance to both glyphosate and glufosinate or to both glypho sate and a herbicide from another class, such as ALS inhibitors, HPPD inhibitors, auxinic herbi cides, or ACCase inhibitors.
  • herbicide resistance technologies are, for example, de scribed in Pest Management Science 61 , 2005, 246; 61 , 2005, 258; 61 , 2005, 277; 61 , 2005, 269; 61 , 2005, 286; 64, 2008, 326; 64, 2008, 332; Weed Science 57, 2009, 108; Australian Journal of Agricultural Research 58, 2007, 708; Science 316, 2007, 1185; and references quot ed therein.
  • Several cultivated plants have been rendered tolerant to herbicides by mutgenesis and conventional methods of breeding, e. g., Clearfield® crops, such as Clearfield® summer rape (Canola, BASF SE, Germany) being tolerant to imidazolinones, e.
  • glufosinate some of which are under development or commercially available under the brands or trade names RoundupReady® (glyphosate tolerant, Monsanto, USA), Cultivance® (imidazo linone tolerant, BASF SE, Germany) and LibertyLink® (glufosinate tolerant, Bayer CropScience, Germany).
  • RoundupReady® glyphosate tolerant, Monsanto, USA
  • Cultivance® imidazo linone tolerant, BASF SE, Germany
  • LibertyLink® glufosinate tolerant, Bayer CropScience, Germany
  • the combinations according to the invention can also be used in genetically modified crop plants.
  • genetically modified plants is to be understood as plants whose genetic mate- rial has been modified by the use of recombinant DNA techniques to include an inserted se quence of DNA that is not native to that plant species’ genome or to exhibit a deletion of DNA that was native to that species’ genome, wherein the modification(s) cannot readily be obtained by cross breeding, mutagenesis or natural recombination alone.
  • a particular genetically modified plant will be one that has obtained its genetic modification(s) by inheritance through a natural breeding or propagation process from an ancestral plant whose genome was the one directly treated by use of a recombinant DNA technique.
  • one or more genes have been integrated into the genetic material of a genetically modified plant in order to improve cer tain properties of the plant.
  • Such genetic modifications also include, but are not limited to tar geted post-translational modification of protein(s), oligo- or polypeptides e. g., by inclusion therein of amino acid mutation(s) that permit, decrease, or promote glycosylation or polymer additions such as prenylation, acetylation farnesylation, or PEG moiety attachment.
  • the combinations according to the invention can also be used in crop plants that have been modified, e.g. by the use of recombinant DNA techniques to be capable of synthesizing one or more insecticidal proteins, especially those known from the bacterial genus Bacillus, particularly from Bacillus thuringiensis, such as delta-endotoxins, e. g., CrylA(b), CrylA(c), CrylF, CrylF(a2), CryllA(b), CrylllA, CrylllB(bl) or Cry9c; vegetative insecticidal proteins (VIP), e. g., VIP1 , VIP2, VIP3 or VIP3A; insecticidal proteins of bacteria colonizing nematodes, e.
  • VIP vegetative insecticidal proteins
  • Photorhabdus spp. or Xenorhabdus spp. toxins produced by animals, such as scorpion toxins, arachnid toxins, wasp toxins, or other insect-specific neurotoxins; toxins produced by fungi, such as Streptomy- cetes toxins, plant lectins, such as pea or barley lectins; agglutinins; proteinase inhibitors, such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin or papain inhibitors; ribosome inactivating proteins (RIP), such as ricin, maize-RIP, abrin, luffin, saporin or bryodin; steroid metabolism enzymes, such as 3- hydroxy- steroid oxidase, ecdysteroid-IDP-glycosyl-transferase, cholesterol oxidases, ecdysone inhibitors or HMG-CoA-reductase;
  • these insecticidal proteins or toxins are to be understood expressly also as including pre-toxins, hybrid proteins, truncated or otherwise modified proteins.
  • Hybrid proteins are characterized by a new combination of protein domains, (see, e. g.,
  • WO 02/015701 Further examples of such toxins or genetically modified plants capable of syn thesizing such toxins are disclosed, e. g., in EP-A 374 753, WO 93/007278, WO 95/34656, EP- A 427 529, EP-A 451 878, WO 03/18810 und WO 03/52073.
  • the methods for producing such genetically modified plants are generally known to the person skilled in the art and are de scribed, e. g., in the publications mentioned above.
  • insecticidal proteins contained in the genetically modified plants impart to the plants producing these proteins tolerance to harmful pests from all taxonomic groups of arthropods, especially to beetles (Coleoptera), two-winged insects (Diptera), and moths (Lepidoptera) and to nematodes (Nematoda).
  • Genetically modified plants capable to synthesize one or more insecticidal proteins are, e.
  • the combinations according to the invention can also be used in crop plants that have been modified, e.g. by the use of recombinant DNA techniques to be capable of synthesizing one or more proteins to increase the resistance or tolerance of those plants to bacterial, viral or fungal pathogens.
  • proteins are the so-called“pathogenesis-related proteins” (PR proteins, see, e.g., EP-A 392 225), plant disease resistance genes (e.
  • potato cultivars which express resistance genes acting against Phytophthora infestans derived from the Mexican wild potato, Solanum bulbocastanum) or T4-lysozym (e.g., potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylovora).
  • T4-lysozym e.g., potato cultivars capable of synthesizing these proteins with increased resistance against bacteria such as Erwinia amylovora.
  • the combinations according to the invention can also be used in crop plants that have been modified, e.g. by the use of recombinant DNA techniques to be capable of synthesizing one or more proteins to increase the productivity (e.g., bio-mass production, grain yield, starch content, oil content or protein content), tolerance to drought, salinity or other growth-limiting environmen tal factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.
  • productivity e.g., bio-mass production, grain yield, starch content, oil content or protein content
  • tolerance to drought e.g., salinity or other growth-limiting environmen tal factors or tolerance to pests and fungal, bacterial or viral pathogens of those plants.
  • the combinations according to the invention can also be used in crop plants that have been modified, e.g. by the use of recombinant DNA techniques to be capable of producing an in creased amount of ingredients or new ingredients, which are suitable to improve human or ani- mal nutrition, e. g., oil crops that produce health-promoting long-chain omega-3 fatty acids or unsaturated omega-9 fatty acids (e. g., Nexera® rape, Dow AgroSciences, Canada).
  • the combinations of the present invention can be applied in a conventional manner by a skilled personal familiar with the techniques of applying herbicides. Suitable techniques include spray ing, atomizing, dusting, spreading or watering. The type of application depends on the intended purpose in a well known manner; in any case, they should ensure the finest possible distribution of the active ingredients according to the invention.
  • the combinations can be applied pre- or post-emergence, i.e. before, during and/or after emer gence of the undesirable plants.
  • the combinations can be applied after seeding and before or after the emergence of the crop plants.
  • the compositions according to the invention can, however, also be applied prior to seeding of the crop plants.
  • the combinations according to the invention have a very good post-emergence herbicide activity, i.e. they show a good herbicidal activity against emerged undesirable plants.
  • the combinations are applied post-emergence, i.e. during and/or after, the emergence of the undesirable plants. It is particularly advantageous to apply the combinations according to the invention post emergent when the undesirable plant starts with leaf development up to flowering. Since the combinations of the present invention show good crop tolerance, even when the crop has already emerged, they can be applied after seeding of the crop plants and, in particular, during or after the emer gence of the crop plants.
  • the herbicide A, the herbicide B, and the optional herbicide C can be applied simul taneously or in succession.
  • the combinations of the invention are applied in the form of a com position containing the combination of the present invention and a formulation additive, such as one or more surfactants.
  • a formulation additive such as one or more surfactants.
  • the compositions are dilute aqueous compositions. Such dilute compositions are usually obtained by tank mixing solo- or combo-formulations, containing the herbicide A, the herbicide B, and the optional herbicide C, which are formulated jointly or separately.
  • compositions are applied to the plants mainly by spraying, in particular foliar spraying.
  • Ap plication can be carried out by customary spraying techniques using, for example, water as car rier and spray liquor rates of 10 to 2000 l/ha or 50 to 1000 l/ha (for example from 50 to 500 l/ha).
  • Application of the herbicidal compositions by the low-volume and the ultra-low-volume method is possible, as is their application in the form of microgranules.
  • the herbicidal mixtures or compositions according to the invention are preferably applied by foliar application.
  • Application may be effect ed, for example, by usual spraying techniques with water as the carrier, using amounts of spray mixture of approx. 50 to 1000 l/ha.
  • the application rate of the herbicide A is generally from 1 to 200 g/ha and in particular from 2 to 100 g/ha or from 5 to 50 g/ha.
  • the application rate of the herbicide B is generally from 1 to 200 g/ha, in particular from 2 to 100 g/ha, preferably from 5 to 50 g/ha.
  • the application rate of aclonifen (calculated as such) is in the range from 100 to 5000 g/ha, preferably in the range from 500 to 3000g/ha.
  • the application rate of bixlozone (calculated as such) is in the range from 10 to 1000 g/ha, preferably in the range from 40 to 400 g/ha.
  • the application rate of carfentrazone (calculated as the free acid) is in the range from 5 to 500 g/ha, preferably in the range from 20 to 300 g/ha.
  • the application rate of clethodim (calculated as such) is in the range from 20 to 1000 g/ha, preferably in the range from 40 to 400 g/ha.
  • the application rate of clomazone (calculated as such) is in the range from 10 to 1000 g/ha, preferably in the range from 40 to 400 g/ha.
  • the application rate of cycloxydim is in the range from 20 to 2000 g/ha, preferably in the range from 100 to 1000 g/ha. If the herbicide C is dimethenamid-P, the application rate of dimethenamid-P (calculated as such) is in the range from 200 to 2000 g/ha, preferably in the range from 400 to 1600 g/ha.
  • the application rate of ethalfluralin (calculated as such) is in the range from 200 to 6000 g/ha, preferably in the range from 400 to 4000 g/ha.
  • the application rate of fluazifop (calculated as the free acid) is in the range from 20 to 500 g/ha, preferably in the range from 50 to 300 g/ha.
  • the application rate of fluazifop-P (calculated as the free acid) is in the range from 20 to 500 g/ha, preferably in the range from 50 to 300 g/ha.
  • the application rate of halauxifen (calculated as the free acid) is in the range from 0.5 to 100 g/ha, preferably in the range from 1 to 20 g/ha.
  • the application rate of haloxyfop (calculated as the free acid) is in the range from 5 to 500 g/ha, preferably in the range from 10 to 300 g/ha.
  • the application rate of haloxyfop-P (calculated as the free acid) is in the range from 5 to 500 g/ha, preferably in the range from 10 to 300 g/ha.
  • the application rate of S-metolachlor (calculated as such) is in the range from 250 to 2500 g/ha, preferably in the range from 400 to 1600 g/ha.
  • the application rate of pendimethalin (calculated as such) is in the range from 250 to 5000 g/ha, preferably in the range from 500 to 3000 g/ha.
  • the application rate of pethoxamid (calculated as such) is in the range from 250 to 2500 g/ha, preferably in the range from 500 to 2000 g/ha.
  • the application rate of prohexadione (calculated as the free acid) is in the range from 250 to 5000 g/ha, preferably in the range from 500 to 3000 g/ha.
  • the application rate of propaquizafop (calculated as such) is in the range from 5 to 500 g/ha, preferably in the range from 10 to 300 g/ha.
  • the application rate of propisochlor is in the range from 200 to 5000 g/ha, preferably in the range from 500 to 3000 g/ha.
  • the application rate of prosulfocarb is in the range from 200 to 5000 g/ha, preferably in the range from 500 to 3000 g/ha.
  • the application rate of pyroxasulfone (calculated as such) is in the range from 10 to 300 g/ha, preferably in the range from 25 to 250 g/ha.
  • the application rate of quizalofop (calculated as the free acid) is in the range from 5 to 300 g/ha, preferably in the range from 10 to 150 g/ha.
  • the application rate of quizalofop-P (calculated as the free acid) is in the range from 5 to 300 g/ha, preferably in the range from 10 to 150 g/ha.
  • the application rate of sethoxydim (calculated as such) is in the range from 10 to 2000 g/ha, preferably in the range from 20 to 400 g/ha.
  • the application rate of sulfentrazone (calculated as such) is in the range from 10 to 2000 g/ha, preferably in the range from 20 to 400 g/ha.
  • the application rate of terbuthylazine (calculated as such) is in the range from 100 to 3000 g/ha, preferably in the range from 250 to 1500 g/ha.
  • the application rate of trifluralin (calculated as such) is in the range from 100 to 3000 g/ha, preferably in the range from 250 to 1500 g/ha.
  • the present invention also relates to compositions and formulations comprising a combination according to the present invention.
  • compositions usually contain, besides the combinations of the invention, at least one formulation additive.
  • the formulation additive comprises one or more surfactants and, optionally, one or more formulation auxiliaries commonly used in crop protection.
  • the compositions include both liquid dilute compositions as well as concentrate formulations containing, besides the active ingredients, at least one organic or inorganic carrier material and one or more formulation additives, in particular one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • compositions of the invention may be used as such or in combination with adjuvants which are conventionally used with herbicides, and which include, in particular, blends of paraffinic oils with non-ionic or anionic surfactants (crop-oils and crop-oil concentrates), blends of esterified vegetable-oils, such as methylated seed oil, and non-ionic or anionic surfactants, blends of veg etable oils and non-ionic or anionic surfactants such as Dash®, Hasten®, Agrirob®, Trend® and Mero®.
  • adjuvants which are conventionally used with herbicides, and which include, in particular, blends of paraffinic oils with non-ionic or anionic surfactants (crop-oils and crop-oil concentrates), blends of esterified vegetable-oils, such as methylated seed oil, and non-ionic or anionic surfactants, blends of veg etable oils and non-ionic or anionic surfactants such as Dash®,
  • Particularly suitable adjuvants comprise a polar solvent and a phosphate ester of the formula (A) in which
  • R 3 IS R 1 -0-(C n H 2n 0) x -(C m H 2m 0) y -,
  • R b is R 1 -0-(C n H 2n 0) x -(C m H 2m 0)y- or OH,
  • R 1 is Ce-Cso-alkyl
  • n, m independently of one another are a value of from 2 to 6,
  • x, y independently of one another are a value of from 0 to 100
  • x+y gives a value of from 1 to 100
  • phosphate ester of the formula (A) can be present as the free acid and/or as a salt and wherein the polar solvent is dimethyl sulfoxide or tetramethylene sulfone.
  • the formulation may be in the form of a single package formulation containing the herbicides A, B, and optionally C, together with liquid and/or solid carrier materials, and one or more formula tion additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • the formulation may be in the form of a two pack age formulation (two kits of parts formulation), wherein one package contains a formulation of herbicide A, while the other package contains a formulation of the herbicide B and C and where in both formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxil iaries customary for crop protection compositions.
  • the formulation may also be in the form of a two package formulation (two kits of parts formulation), wherein one package contains a formu lation of herbicides A and B, while the other package contains a formulation of the herbicide C, and wherein both formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • a two package formulation two kits of parts formulation
  • one package contains a formu lation of herbicides A and B
  • the other package contains a formulation of the herbicide C
  • both formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • the formulation may also be in the form of a two package formulation (two kits of parts formulation), wherein one package contains a formulation of herbicide A, while the other package contains a formulation of the herbicide B, and wherein both formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • a two package formulation two kits of parts formulation
  • one package contains a formulation of herbicide A
  • the other package contains a formulation of the herbicide B
  • both formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • the formulation may also be in the form of a three package formulation (three kits of parts formulation), wherein one package contains a formulation of herbicide compound A, a second package contains the herbicide B, and a third package which contains a formulation of the herbicide C, and wherein the three formulations contain at least one liquid and/or solid carrier material and one or more formulation additives, such as one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions.
  • the two or three formulations are preferably mixed prior to application.
  • the mixing is performed as a tank mix, i.e. the formulations are mixed immediately prior or upon dilution with water.
  • the active ingredients i.e. the herbicides A, B, and optionally C
  • the active ingredients may be present in suspended, emulsified or dissolved form.
  • the formulations ac cording to the invention can be in the form of aqueous solutions, powders, suspensions, also highly-concentrated aqueous, oily or other suspensions or dispersions, aqueous emulsions, aqueous microemulsions, aqueous suspo-emulsions, oil dispersions, pastes, dusts, materials for spreading or granules.
  • the formulation type and the active ingredient they comprise one or more liquid or solid carriers, if appropriate, surfactants (such as dispersants, protective colloids, emulsifiers, wetting agents and tackifiers), and, if appropriate, further auxiliaries which are customary for formulating crop protection products.
  • surfactants such as dispersants, protective colloids, emulsifiers, wetting agents and tackifiers
  • further auxiliaries which are customary for formulating crop protection products.
  • Further auxiliaries include e.g. organic and inorganic thickeners, bactericides, antifreeze agents, antifoams, colorants and, for seed formulations, adhesives.
  • Suitable carriers include liquid and solid carriers.
  • Liquid carriers include e.g. non-aqueous sol vents, such as cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahydronaphthalene, alkylat ed 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 as well as mix tures thereof.
  • Solid carriers include e.g.
  • 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, fertilizers, such as ammoni um sulfate, ammonium phosphate, ammonium nitrate, ureas, and products of vegetable origin, such as cereal meal, tree bark meal, wood meal and nutshell meal, cellulose powders, or other solid carriers.
  • 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, fertilizers, such as ammoni um sulfate, ammonium phosphate, ammonium nitrate, ureas
  • Suitable surfactants are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, for example lignosulfonic acids (e.g.
  • polyoxyethylene alkyl ethers or polyoxypropylene alkyl ethers lauryl alcohol polyglycol ether acetate, sorbitol esters, lignosulfite waste liquors and proteins, denaturated proteins, polysaccharides (e.g. methylcellulose), hydrophobically modified starches, polyvinyl alcohol (Mowiol types Clariant), polycarboxylates (BASF SE, Sokalan types), polyalkoxylates, polyvinylamine (BASF SE, Lupamine types), polyethyleneimine (BASF SE, Lupasol types), polyvinylpyrrolidone and copolymers thereof.
  • Suitable further formulation auxiliaries are e.g. thickeners, antifoams, bactericides, antifreeze agents, colourants and adhesives.
  • thickeners i.e. compounds which impart to the formulation modified flow properties, i.e. high viscosity in the state of rest and low viscosity in motion
  • polysaccharides such as xanthan gum (Kelzan® from Kelco), Rhodopol® 23 (Rhone Poulenc) or Veegum® (from R.T. Vanderbilt), and also organic and inorganic sheet minerals, such as Attaclay® (from Engel hardt).
  • antifoams examples include silicone emulsions (such as, for example, Silikon ® SRE, Wacker or Rhodorsil® from Rhodia), long-chain alcohols, fatty acids, salts of fatty acids, organofluorine compounds and mixtures thereof.
  • Bactericides can be added for stabilizing the aqueous herbicidal formulations.
  • bactericides are bactericides based on diclorophen and benzyl alcohol hemiformal (Proxel® from ICI or Acticide® RS from Thor Chemie and Kathon® MK from Rohm & Haas), and also isothiazolinone derivates, such as alkylisothiazolinones and benzisothiazolinones (Acticide MBS from Thor Chemie).
  • antifreeze agents are ethylene glycol, propylene glycol, urea or glycerol.
  • colorants are both sparingly water-soluble pigments and water-soluble dyes. Examples which may be mentioned are the dyes known under the names Rhodamin B, C.l. Pigment Red 112 and C.l. Solvent Red 1 , and also pigment blue 15:4, pigment blue 15:3, pigment blue 15:2, pigment blue 15: 1 , pigment blue 80, pigment yellow 1 , pigment yellow 13, pigment red 112, pigment red 48:2, pigment red 48:1 , pigment red 57:1 , pigment red 53:1 , pigment orange 43, pigment orange 34, pigment orange 5, pigment green 36, pigment green 7, pigment white 6, pigment brown 25, basic violet 10, basic violet 49, acid red 51 , acid red 52, acid red 14, acid blue 9, acid yellow 23, basic red 10, basic red 108.
  • adhesives are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose.
  • the active the components can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier.
  • wetting agent tackifier
  • dispersant or emulsifier emulsifier
  • concentrates consisting of active substance, 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 the components with a solid carrier.
  • Granules e.g. coated granules, impregnated granules and homogeneous granules, can be pre pared by binding the active ingredients to solid carriers.
  • the formulations of the invention comprise a herbicidally effective amount of the composition of the present invention.
  • concentrations of the active ingredients in the formulations can be varied within wide ranges.
  • the formulations comprise from 1 to 98% by weight, pref erably 10 to 60% by weight, of active ingredients (sum of herbicide compound A, herbicide compound B and herbicide compound C).
  • the active ingredients are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum).
  • compositions according to the invention can, for example, be formulated as follows:
  • polyvinylpyrrolidone Dilution with water gives a dispersion.
  • the active compound content is 20% by weight.
  • the formulation has an active compound content of 15% by weight.
  • 25 parts by weight of the herbicides A, B, and optionally C are dissolved in 35 parts by weight of an organic solvent (e.g. alkylaromatics) with addition of calcium dodecylbenzenesulfonate and castor oil ethoxylate (in each case 5 parts by weight).
  • an organic solvent e.g. alkylaromatics
  • This mixture is introduced into 30 parts by weight of water by means of an emulsifier (Ultraturrax) and made into a homogeneous emulsion. Dilution with water gives an emulsion.
  • the formulation has an active compound content of 25% by weight.
  • the herbicides A, B, and optionally C are comminuted with addition of 10 parts by weight of dispersants and wetters and 70 parts by weight of water or an organic solvent to give a fine active compound suspension. Dilution with water gives a stable suspension of the active compound.
  • the active compound content in the formulation is 20% by weight.
  • 50 parts by weight of the herbicides A, B, and optionally C are ground finely with addition of 50 parts by weight of dispersants and wetters and made into water-dispersible or water-soluble granules by means of technical appliances (for example extrusion, spray tower, fluidized bed). Dilution with water gives a stable dispersion or solution of the active compound.
  • the formulation has an active compound content of 50% by weight.
  • the herbicides A, B, and optionally C are ground in a rotor-stator mill with addition of 25 parts by weight of dispersants, wetters and silica gel. Dilution with water gives a stable dispersion or solution of the active compound.
  • the active compound content of the formulation is 75% by weight.
  • 0.5 parts by weight of the herbicides A, B, and optionally C are ground finely and associated with 99.5 parts by weight of carriers.
  • Current methods here are extrusion, spray-drying or the fluidized bed. This gives granules to be applied undiluted with an active compound content of 0.5% by weight.
  • Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wetta- ble powders or water-dispersible granules by adding water.
  • compositions of the invention alone or in combination with other herbicides, or else in the form of a mixture with other crop protection agents, for example together with agents for controlling pests or phytopathogenic fungi or bacteria.
  • other crop protection agents for example together with agents for controlling pests or phytopathogenic fungi or bacteria.
  • miscibility with mineral salt solutions which are employed for treating nutritional and trace element deficiencies.
  • Other additives such as non-phytotoxic oils and oil concentrates, may also be added.
  • the culture containers used were plastic pots containing loamy sand with approximately 3.0% of humus as substrate.
  • the seeds of the test plants were sown separately for each species.
  • a tank mix containing formulations of the herbicide A, the herbicide B and the herbicide C which had been suspended or emulsified in water were applied by means of finely/evenly distributing spray nozzles.
  • plants were grown in a greenhouse environment.
  • test plants were grown to growth stage 10 to 22, depending on the plant variety or to a height, depending on the plant habit, and only then treated with the active compounds which had been suspended or emulsified in water. To this end, the test plants were either sown directly and grown in the same containers or they were first grown separately as seedlings and transplanted into the test containers a few days prior to treatment.
  • the plants were kept at 10 - 25°C and 20 - 35°C, respectively.
  • the test period extended over 1 to 4 weeks. During this time, the plants were tended and their re sponse to the individual treatments was evaluated.
  • the herbicide compounds applied in the examples were used as commercially available formu lations which have been diluted with tap water to a suitable concentration.
  • the evaluation for the damage caused by the chemical compositions was carried out using a scale from 0 to 100%, compared to the untreated control plants.
  • 0 means no damage and 100 means complete destruction of the plants.
  • X effect in percent using herbicide A + B at an application rate a or a+b, respectively;
  • the value E corresponds to the effect (plant damage or injury) which is to be expected if the activity of the individual compounds is just additive. If the observed effect is higher than the val ue E calculated according to Colby, a synergistic effect is present.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Dentistry (AREA)
  • Plant Pathology (AREA)
  • Engineering & Computer Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Agronomy & Crop Science (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

La présente invention concerne des combinaisons à action herbicide constituées d'herbicides A, B et éventuellement C, a) l'herbicide A étant du R-imazamox, tout mélange non racémique de R-imazamox et de S-imazamox, la proportion de R-imazamox étant d'au moins 80 % en poids, ou un sel ou ester associé acceptable en agriculture ; et b) l'herbicide B étant de l'imazapyr, ou un sel ou ester associé acceptable en agriculture; et c) l'herbicide facultatif C est choisi dans le groupe constitué par les composés suivants : aclonifen, bixlozone, carfentrazone, cléthodim, clomazone, cycloxydim, diméthenamide-P, ethalfluraline, fluazifop, fluazifop-P, halauxifène, haloxyfop, haloxyfop-P, S-métolachlore, pendiméthaline, péthoxamide, prohéxadione-calcium, propaquizafop, propisochloro, prosulfocarb, pyroxasulfone, quizalofop, quizalofop-P, séthoxydim, sulfentrazone, terbuthym, trifluraline, et sels et esters associés.
PCT/EP2019/084125 2018-12-18 2019-12-09 Combinaisons herbicides WO2020126579A1 (fr)

Priority Applications (2)

Application Number Priority Date Filing Date Title
EP19829413.4A EP3897138A1 (fr) 2018-12-18 2019-12-09 Combinaisons herbicides
EA202191587A EA202191587A1 (ru) 2018-12-18 2019-12-09 Гербицидные комбинации

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP18213628.3 2018-12-18
EP18213628 2018-12-18

Publications (1)

Publication Number Publication Date
WO2020126579A1 true WO2020126579A1 (fr) 2020-06-25

Family

ID=64745933

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/EP2019/084125 WO2020126579A1 (fr) 2018-12-18 2019-12-09 Combinaisons herbicides

Country Status (3)

Country Link
EP (1) EP3897138A1 (fr)
EA (1) EA202191587A1 (fr)
WO (1) WO2020126579A1 (fr)

Citations (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
EP0913089A1 (fr) 1997-10-31 1999-05-06 American Cyanamid Company Composition herbicide synergique comprenant le mélange R-imazethapyr/R-imazapyr et procédé de lutte contre les mauvaises herbes
US6060430A (en) * 1997-10-31 2000-05-09 American Cyanamid Company Methods and compositions for enhancing herbicidal activity
EP1050533A1 (fr) 1999-05-03 2000-11-08 American Cyanamid Company Procédé de préparation d'herbicides à base d'imidazolinones chiraux
US6214768B1 (en) 1998-09-14 2001-04-10 American Cyanamid Co. Synergistic herbicidal methods and compositions
US6339158B1 (en) 1999-05-03 2002-01-15 American Cyanamid Co. Process for the preparation of chiral nicotinic, quinolinic or benzoic acid imidazolinone herbicides
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
US6673748B1 (en) 1999-04-09 2004-01-06 Basf Aktiengesellschaft Synergistic herbicidal methods and compositions comprising dinitroaniline and imidazolinone compounds
US20070238618A1 (en) * 2006-04-07 2007-10-11 Basf Aktiengesellschaft Herbicidal mixture, comprising an imidazolinone herbicide and an adjuvant
US20070281859A1 (en) * 2004-04-01 2007-12-06 Basf Akiengesellschaft Synergistically Acting Herbicidal Mixtures
US20080305954A1 (en) * 2005-12-23 2008-12-11 Basf Se Method of Controlling the Aquatic Weed Hydrilla Verticillata
WO2009112454A2 (fr) 2008-03-10 2009-09-17 Basf Se Compositions herbicides comprenant de la pyroxasulfone
US20140073510A1 (en) * 2011-05-03 2014-03-13 Basf Se Adjuvant Comprising Dimethylsulfoxide and a Phosphate Ester
CN107602533A (zh) * 2017-08-15 2018-01-19 浙江大学 一种r‑甲氧咪草烟的制备方法及用途

Patent Citations (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0451878A1 (fr) 1985-01-18 1991-10-16 Plant Genetic Systems, N.V. Modification de plantes par techniques de génie génétique pour combattre ou contrôler les insectes
EP0374753A2 (fr) 1988-12-19 1990-06-27 American Cyanamid Company Toxines insecticides, gènes les codant, anticorps les liant, ainsi que cellules végétales et plantes transgéniques exprimant ces toxines
EP0392225A2 (fr) 1989-03-24 1990-10-17 Ciba-Geigy Ag Plantes transgéniques résistantes aux maladies
EP0427529A1 (fr) 1989-11-07 1991-05-15 Pioneer Hi-Bred International, Inc. Lectines larvicides, et résistance induite des plantes aux insectes
WO1993007278A1 (fr) 1991-10-04 1993-04-15 Ciba-Geigy Ag Sequence d'adn synthetique ayant une action insecticide accrue dans le mais
WO1995034656A1 (fr) 1994-06-10 1995-12-21 Ciba-Geigy Ag Nouveaux genes du bacillus thuringiensis codant pour des toxines actives contre les lepidopteres
EP0913089A1 (fr) 1997-10-31 1999-05-06 American Cyanamid Company Composition herbicide synergique comprenant le mélange R-imazethapyr/R-imazapyr et procédé de lutte contre les mauvaises herbes
US6060430A (en) * 1997-10-31 2000-05-09 American Cyanamid Company Methods and compositions for enhancing herbicidal activity
US6214768B1 (en) 1998-09-14 2001-04-10 American Cyanamid Co. Synergistic herbicidal methods and compositions
US6673748B1 (en) 1999-04-09 2004-01-06 Basf Aktiengesellschaft Synergistic herbicidal methods and compositions comprising dinitroaniline and imidazolinone compounds
US6339158B1 (en) 1999-05-03 2002-01-15 American Cyanamid Co. Process for the preparation of chiral nicotinic, quinolinic or benzoic acid imidazolinone herbicides
EP1050533A1 (fr) 1999-05-03 2000-11-08 American Cyanamid Company Procédé de préparation d'herbicides à base d'imidazolinones chiraux
WO2002015701A2 (fr) 2000-08-25 2002-02-28 Syngenta Participations Ag Nouvelles toxines insecticides derivees de proteines cristallines insecticides de $i(bacillus thuringiensis)
WO2003018810A2 (fr) 2001-08-31 2003-03-06 Syngenta Participations Ag Toxines cry3a modifiees et sequences d'acides nucleiques les codant
WO2003052073A2 (fr) 2001-12-17 2003-06-26 Syngenta Participations Ag Nouvel evenement du mais
US20070281859A1 (en) * 2004-04-01 2007-12-06 Basf Akiengesellschaft Synergistically Acting Herbicidal Mixtures
US20080305954A1 (en) * 2005-12-23 2008-12-11 Basf Se Method of Controlling the Aquatic Weed Hydrilla Verticillata
US20070238618A1 (en) * 2006-04-07 2007-10-11 Basf Aktiengesellschaft Herbicidal mixture, comprising an imidazolinone herbicide and an adjuvant
WO2009112454A2 (fr) 2008-03-10 2009-09-17 Basf Se Compositions herbicides comprenant de la pyroxasulfone
US20140073510A1 (en) * 2011-05-03 2014-03-13 Basf Se Adjuvant Comprising Dimethylsulfoxide and a Phosphate Ester
CN107602533A (zh) * 2017-08-15 2018-01-19 浙江大学 一种r‑甲氧咪草烟的制备方法及用途

Non-Patent Citations (15)

* Cited by examiner, † Cited by third party
Title
"The Pesticide Manual", 2006, BCPC ALTON, pages: 587
AUSTRALIAN JOURNAL OF AGRICULTURAL RESEARCH, vol. 58, 2007, pages 708
BULL ENVI-RON CONTAM TOXICOL, vol. 96, 2016, pages 242 - 247
C. WANG ET AL.: "Enantioselective Phytotoxicity and the Relative Mechanism of Chiral Herbicides", CURRENT PROTEIN AND PEPTIDE SCIENCE, 2017, pages 15 - 21
CHRISTIAN WILLENBORG ET AL: "Emergence timing and management of cleavers in Saskatchewan canola crops", PROJECT FINAL REPORT - ADF20120028, 1 October 2015 (2015-10-01), pages 1 - 40, XP055563889, Retrieved from the Internet <URL:https://www.saskcanola.com/quadrant/System/research/reports/ADF_20120028_Willenborg_Final_Report_Cleavers.pdf> [retrieved on 20190301] *
DESMOND BROWN ET AL: "Evaluation of Herbicides for Pumpkin (Cucurbita spp.) 1", WEED TECHNOLOGY, vol. 16, no. 2, 1 April 2002 (2002-04-01), US, pages 282 - 292, XP055563473, ISSN: 0890-037X, DOI: 10.1614/0890-037X(2002)016 0282:EOHFPC!2.0.CO;2 *
JULIO A. SCURSONI ET AL: "Impact of Imazamox and Imazapyr Carryover on Wheat, Barley, and Oat", WEED TECHNOLOGY, vol. 31, no. 06, 1 December 2017 (2017-12-01), US, pages 838 - 846, XP055564901, ISSN: 0890-037X, DOI: 10.1017/wet.2017.66 *
MIRA KNEZEVIC ET AL: "EFFICACY OF SOME HERBICIDES FOR PRE- AND POSTEMERGENCE WEED CONTROL IN SOYBEAN (Abstract)", HERBOLOGIA, vol. 10, no. 2, 1 December 2009 (2009-12-01), pages 65 - 74, XP055563891, DOI: http://eds.b.ebscohost.com/eds/detail/detail?vid=0&sid=8ec61bc9-5e4a-465b-a7fc-682ae5029f98%40pdc-v-sessmgr03&bdata=JnNpdGU9ZWRzLWxpdmU%3d#db=asx&AN=48973383 *
PEST MANAGEMENT SCIENCE, vol. 61, 2005, pages 246
PEST MANAGEMENT SCIENCE, vol. 61, 2005, pages 286
PEST MANAGEMENT SCIENCE, vol. 64, 2008, pages 332
S. R. COLBY: "Calculating synergistic and antagonistic responses of herbicide combinations", WEEDS, vol. 15, 1967, pages 22 ff
S.A. WALTERS ET AL: "WEED CONTROL IN NO-TILLAGE ZUCCHINI SQUASH PRODUCTION", ACTA HORTICULTURAE, no. 638, 1 June 2004 (2004-06-01), BE, pages 201 - 207, XP055563881, ISSN: 0567-7572, DOI: 10.17660/ActaHortic.2004.638.26 *
SCIENCE, vol. 316, 2007, pages 1185
WEED SCIENCE, vol. 57, 2009, pages 108

Also Published As

Publication number Publication date
EP3897138A1 (fr) 2021-10-27
EA202191587A1 (ru) 2021-10-20

Similar Documents

Publication Publication Date Title
AU2012215446B2 (en) Herbicidal compositions comprising topramezone and pinoxaden
AU2009224666B2 (en) Herbicidal compositions comprising pyroxasulfone VII
AU2016294380A1 (en) Herbicidal composition comprising cinmethylin and pyroxasulfone
AU2016292569A1 (en) Herbicidal composition comprising cinmethylin and specific pigment synthesis inhibitors
HUE025377T2 (en) Herbicidal compositions containing chloroacetamides
AU2010209649A1 (en) Herbicidal compositions comprising naptalam
WO2014033242A1 (fr) Utilisation d&#39;une composition agrochimique à action herbicide dans la culture du riz
EP2787814B1 (fr) Contrôle de la végétation indesiderable avec d&#39;imazamox et des adjuvants dans des plantes utiles resistantes aux herbicides
WO2020126584A1 (fr) Combinaisons herbicides
EP3897138A1 (fr) Combinaisons herbicides
EP3897137A1 (fr) Combinaisons herbicides
WO2020126583A1 (fr) Combinaisons herbicides
WO2020126582A1 (fr) Combinaisons herbicides
EP3897151A1 (fr) Composition herbicide
BR102015029158A2 (pt) composições herbicidas, utilização das composições, método para controle da vegetação e formulação herbicida
US20150150259A1 (en) Use of an agrochemical composition with herbicidal action in corn
WO2013127845A1 (fr) Utilisation d&#39;une composition agrochimique à action fongicide, herbicide et améliorant la santé des plantes avec le tournesol
WO2013127862A1 (fr) Utilisation d&#39;une composition agrochimique ayant une action herbicide sur le colza
WO2013127821A1 (fr) Utilisation d&#39;une composition agrochimique à action fongicide et améliorant la santé des plantes avec le colza

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 19829413

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

ENP Entry into the national phase

Ref document number: 2019829413

Country of ref document: EP

Effective date: 20210719