EP3897140A1 - Herbicidal combinations - Google Patents

Abstract

The present invention relates to herbicidally active combinations consisting of herbicides A, B, and optionally C, wherein a.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 agriculturally ac- ceptable salt or ester thereof; and b.the herbicide B is quinmerac, or an agriculturally acceptable salt or ester thereof; and c.the optional herbicide C is selected from the group consisting of aminopyralid, bixlozone, clethodim, clomazone, clopyralid, cycloxydim, dimethachlor, DMTA-p, ethametsulfuron, flua- zifop-P, halauxifen, haloxyfop-P, metazachlor, napropamide, napropamide-M, pendime- thalin, pethoxamid, picloram, propaquizafop, propisochlor, propyzamide, pyroxasulfone, quizalofop, quizalofop-P, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)-2- pyridinecarboxylic acid and the salts and esters thereof.

Description

Herbicidal Combinations

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.

Background of the invention

In crop protection, it is principally desirable to increase the specificity and the reliability of the action of active compounds. For herbicides in particular, it is desirable that the 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). Imazamox pro vides highly effective control of several annual and perennial grass and broadleaf weed species. Imazamox is registered for several legume crops and imidazolinone tolerant crops, such as rice, wheat, corn, lentil, sunflower and oilseed rape (canola). Imidazolinone tolerant crops are also termed Clearfield® crops. The herbicidal activity and the activity spectrum, however, are some times limited. In order to achieve a reliable herbicidal action, it has been recommended to apply imazamox in combination with adjuvants, such as Dash®. Formulations of imazamox, compris ing 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.

Processes for the synthesis of the R-enantiomer of imazamox are known from EP 1 050 533 and US 6,339,158.

The herbicidal effect of combinations of the R-enantiomer of an imidazolinone compound and the R-enantiomer of a second different imidazolinone compound, such as R-imazamox + R- imazapyr, R-imazamox + R-imazaquin, and R-imazamox + R-imazethapyr, was described in EP 913 089. Furthermore, the combination of R-imazethapyr + R-imazapyr demonstrated crop se lectivity; no or slight injury, such as stunting or chlorosis, was observed in imidazolinone tolerant corn. Control of pitted morningglory and purple nutsedge by combinations of R-imazamox + glyphosate is described in US6,214,768.

Quinolinecarboxylic acid herbicides, such as quinclorac and quinmerac as well as their salts and esters, are commonly used for controlling grass weeds and some broadleaf weeds (see C.D.S Tomlin (Ed.), The Pesticide Manual, 14th ed., 2006, BCPC Alton, Hampshire, UK, p. 928 ff. for further references). Both herbicides belong to the group of synthetic auxins. Quinmerac (lUPAC: 7-chloro-3-methylquinoline-8-carboxylic acid) is frequently used with co-herbicides. The herbicidal activity and the activity spectrum, however, is only limited.

W02005/096814 teaches that co-application of imidazolinone herbicides, including R- imazamox, with certain other herbicides, such as chloroacetamides or quinmerac, may lead to a synergistic herbicidal activity.

Mixtures comprising aminopyralid, imazamox and quinmerac and further active herbicides are disclosed in WO09/153246. W017/009060 describes mixtures of cinmethylin with imazamox and quinmerac.

Jing Wei et al. found that the chiral herbicide imazamox poses enantioselective phytotoxicity on maize seedlings: the order of toxicity is R-imazamox > Rac-imazamox > S-imazamox ( Bull Envi ron Contam Toxicol (2016) 96:242-247).

C. Wang et al. discuss in their review on“Enantioselective Phytotoxicity and the Relative Mech anism of Chiral Herbicides” ( Current Protein and Peptide Science, 2017, 15-21) enantioselec tive phytotoxicity of chiral herbicides, i.a. of the imidazolinone Imazapyr. The authors find that the herbicidally active enantiomer, R-imazapyr, displayed more phytotoxicity to non-target plants. They conclude that the reason for the impediment to the development of enantiomer enriched herbicides could be partially attributed to the beneficial balance between/among enan tiomers on the herbicidal activity and ecological safety (i.e. phytotoxicity).

Summary of the invention

It is an object of the present invention to provide combinations of herbicides which show en hanced herbicide action against undesirable harmful plants and/or improved compatibility with crop plants, in particular improved compatibility with legumes, such as lentils, peas, soy beans, beans or crop plants which are tolerant to herbicides which inhibit acetolactate synthase (ALS tolerant crops), in particular 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 with ALS tolerant corn, ALS tolerant sugar beet, ALS tolerant potato, ALS toler ant rice, ALS tolerant sunflower and/or ALS tolerant oilseed rape (canola). 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.

Furthermore, 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).

We have found that these and further objects are achieved, surprisingly, by herbicidally active combinations consisting of herbicides A, B, and optionally C, wherein

a. 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 agriculturally ac ceptable salt or ester thereof; and

b. the herbicide B is quinmerac, or an agriculturally acceptable salt or ester thereof; and c. the optional herbicide C is selected from the group consisting of aminopyralid, bixlozone, clethodim, clomazone, clopyralid, cycloxydim, dimethachlor, dimethenamid-P, ethametsulfu- ron, fluazifop-P, halauxifen, haloxyfop-P, metazachlor, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, propisochlor, propyzamide, pyroxasul- fone, quizalofop, quizalofop-P, 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)-2- pyridinecarboxylic acid (W02014/151005, CAS 1628702-28-2), and the salts and esters thereof.

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, corn, rice, sunflower, lentils, peas and oilseed rape (canola), preferably oilseed rape (canola).

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.

In the methods of the present invention, it is immaterial, whether 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.

Detailed description of the invention Surprisingly, 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. In other words, 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. For this reason, 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.

Moreover, 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. Moreover, 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.

As used herein, the terms "controlling" and "combating" are synonyms.

As used herein, the terms "undesirable vegetation" and "harmful plants" are synonyms.

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.

When using the combination of the invention for this purpose, 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.

The term "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. The term "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.

The term "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.

As imazamox is a carboxylic acid, 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-C₄-alkoxy-CrC₄- alkoxycarbonyl group. Examples of esters are the methyl, ethyl, propyl, isopropyl, butyl, isobu tyl, pentyl, mexyl (1-methylhexyl) or isooctyl (2-ethylhexyl) esters. Examples of 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. Usually, 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 CrCe-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- thylammonium, tetrabutylammonium, pentylammonium, hexylammonium, heptylammonium, 2- hydroxyethylammonium (olamine salt), 2-(2-hydroxyethoxy)eth-1-ylammonium (diglycolamine salt), di(2-hydroxyeth-1-yl)ammonium (= diethanolammonium salt or diolamine salt), tri(2- hydroxyethyl)ammonium (= triethanolammonium salt or trolamine salt), mono-, di- and tri(hydroxypropyl)ammonium (= mono-, di- and tripropanolammonium), benzyltrimethylammoni- um, benzyltriethylammonium, furthermore phosphonium ion salts and sulfonium salts, e.g. tri(Ci-C4-alkyl)sulfonium such as trimethylsulfonium, and sulfoxonium salts.

The combinations of the invention contain the herbicide B, which is quinmerac, or an agricultur ally acceptable salt or ester thereof. As quinmerac is a carboxylic acid, the combination may comprise quinmerac as such (B-1) or as a salt (B-2), in particular an alkalimetal salt or an am monium salt or substituted ammonium salt as defined above for the herbicide A. The carboxyl group of quinmerac may also be present in esterified form, e.g. in the form of a CrCs- alkoxycarbonyl group or in the form of a Ci-C4-alkoxy-Ci-C4-alkoxycarbonyl group. Examples of esters are the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, mexyl (1-methylhexyl) or isooctyl (2-ethylhexyl) esters. Examples of Ci-C4-alkoxy-CrC4-alkyl esters are the straight-chain or branched CrC4-alkoxyethyl esters, for example the methoxyethyl, ethoxyethyl or butoxyethyl (butoyl) esters. Usually, the combinations of the invention contain quinmerac as such or as a salt thereof, in particular as an alkalimetal salt or an ammonium salt as defined above for the herbicide A.

In the combinations of the present invention, the relative weight ratio of the herbicide A, calcu lated as free acid of imazamox, to the herbicide B, calculated as free acid of quinmerac, is in the range from 1 :60 to 1 :2, in particular from 1 :40 to 1 :3, especially from 1 :30 to 1 :4. Preferably, the relative weight ratio is in the range from 1 :20 to 1 :5. Accordingly, in the methods 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 aminopyralid, bixlozone, clethodim, clomazone, clopyralid, cy- cloxydim, dimethachlor, dimethenamid-P, ethametsulfuron, fluazifop-P, halauxifen, haloxyfop-P, metazachlor, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, propisochlor, propyzamide, pyroxasulfone, quizalofop, quizalofop-P, 4-amino-3- chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid, and the salts and esters thereof.

In one embodiment, the combinations of the present invention may contain a third herbicide C, which is selected from the group consisting of bixlozone, clethodim, clomazone, clopyralid, cy- cloxydim, dimethachlor, dimethenamid-P, ethametsulfuron, fluazifop-P, halauxifen, haloxyfop-P, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, propiso chlor, propyzamide, pyroxasulfone, quizalofop, quizalofop-P, 4-amino-3-chloro-5-fluoro-6-(7- fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid, and the salts and esters thereof.

In another embodiment, the combinations of the present invention may contain a third herbicide C, which is selected from the group consisting of bixlozone, clethodim, clomazone, clopyralid, cycloxydim, dimethachlor, dimethenamid-P, ethametsulfuron, fluazifop-P, halauxifen, haloxyfop- P, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, pro pisochlor, propyzamide, quizalofop, quizalofop-P, and the salts and esters thereof.

Optional herbicides C:

C-1. aminopyralid

lUPAC name: 4-amino-3,6-dichloropyridine-2-carboxylic acid.

Manufacture and herbicidal action are described in WO 01/51468. Exemplary agriculturally ac ceptable salts or esters of aminopyralid include aminopyralid-dimethylammonium, aminopyralid- potassium, aminopyralid-tris(2- hydroxypropyl)ammonium, aminopyralid-triisopropanolammonium salt (TIPA), and mixtures thereof.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-1 , is preferably in the range from 1 :20 to 20:1 , in particular from 1 :10 to 10:1 , espe cially from 1 :2 to 8:1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-1 is calculated as the free acid. 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.

C-2. bixlozone

lUPAC name: 2-(2,4-dichlorobenzyl)-4,4-dimethylisoxazolidin-3-one.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-2, is preferably in the range from 1 :60 to 2:1 , in particular from 1 :30 to 1 :1 , especial- ly 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.

C-3. clethodim

lUPAC name: (5RS)-2-[(1 £Z)-1-[(2£)-3-chloroallyloxyimino]propyl]-5-[(2RS)-2-(ethylthio)propyl]- 3-hydroxycyclohex-2-en-1-one.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-3, is preferably in the range from 1 :60 to 2: 1 , in particular from 1 :30 to 1 : 1 , especial ly 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-3 is calculated as such. 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.

C-4. clomazone

lUPAC name: 2-(2-chlorobenzyl)-4,4-dimethyl-1 ,2-oxazolidin-3-one.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-4, is preferably in the range from 1 :60 to 2: 1 , in particular from 1 :30 to 1 : 1 , especial ly 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-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.

C-5. clopyralid

lUPAC name: 3,6-dichloropicolinic acid.

Exemplary agriculturally acceptable salts or esters of clopyralid include clopyralid-potassium, clopyralid-olamine, clopyralid-triethylammonium, clopyralid-tris(2-hydroxypropyl)ammonium, clopyralid-methyl, and mixtures thereof. In some embodiments, clopyralid is provided as an amine salt, such as clopyralid-olamine salt, dimethylamine (DMA) salt, monoethanolamine (MEA) salt, triisopropanolamine (TIPA) salt, and mixtures thereof.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-5, is preferably in the range from 1 :50 to 2: 1 , in particular from 1 :40 to 1 : 1 , especial ly from 1 :30 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-5 is calculated as the free acid. 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.

C-6. cycloxydim

lUPAC name: (5RS)-2-[(£Z)-1-(ethoxyimino)butyl]-3-hydroxy-5-[(3RS)-thian-3-yl]cyclohex-2-en- 1-one.

In the combinations of the present invention, 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 :100 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.

C-7. dimethachlor

CAS name: 2-chloro-/\/-(2,6-dimethylphenyl)-/\/-(2-methoxyethyl)acetamide.

In the combinations of the present invention, 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 :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-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.

C-8. dimethenamid-P

lUPAC name: (S)-2-chloro-/\/-(2,4-dimethyl-3-thienyl)-/\/-(2-methoxy-1-methylethyl)acetamide (abbr. DMTA-P).

In the combinations of the present invention, 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.

C-9. ethametsulfuron lUPAC name: (2-[(4-ethoxy-6-methylamino-1 ,3,5-triazin-2-yl)carba oylsulfa oyl]benzoic acid (common name: ethametsulfuron).

Exemplary agriculturally acceptable salts or esters of ethametsulfuron include ethametsulfuron- methyl.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-9, is preferably in the range from 1 :20 to 20: 1 , in particular from 1 :5 to 5: 1 , especial ly from 1 :2 to 2: 1 , 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.

C-10. fluazifop-P

lUPAC name: (R)-2-[4-(5-trifluoromethyl-2-pyridyloxy)phenoxy]propionic acid.

Exemplary agriculturally acceptable salts or esters of fluazifop-P include fluazifop-P-butyl.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-10, is preferably in the range from 1 :200 to 2: 1 , in particular from 1 :100 to 1 : 1 , es pecially from 1 :50 to 1 :2, wherein the herbicide A is calculated as the free acid form of imaza mox and wherein the herbicide compound C-10 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-10 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-10 within these weight ratios.

C-1 1. halauxifen

lUPAC name: 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylic ac id.

Exemplary agriculturally acceptable salts or esters of halauxifen include halauxifen-methyl.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-11 , is preferably in the range from 1 :3 to 30: 1 , in particular from 1 :2 to 20: 1 , espe cially from 1 : 1 to 10: 1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-1 1 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-1 1 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-1 1 within these weight ratios.

C-12. haloxyfop-P

lUPAC name: (R)-2-[4-(3-chloro-5-(trifluoromethyl)-2-pyridyloxy)phenoxy]propionic acid. Exem plary agriculturally acceptable salts or esters of haloxyfop-P include haloxyfop-P-methyl. In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-12, is preferably in the range from 1 : 100 to 4: 1 , in particular from 1 :50 to 2:1 , espe cially from 1 :20 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. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-12 are preferably ap plied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-12 within these weight ratios.

C-13. metazachlor

CAS name: 2-chloro-/\/-(2,6-dimethylphenyl)-/\/-(1 /-/-pyrazol-1-ylmethyl)acetamide.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-13, is preferably in the range from 1 :200 to 2: 1 , in particular from 1 :100 to 1 : 1 , 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-13 is calculated as such. Accordingly, in the meth ods and uses of the invention, the herbicide A and the herbicide C-13 are preferably applied within these weight ratios. Likewise, the compositions and formulations of the invention contain the herbicide A and the herbicide C-13 within these weight ratios.

C-14. napropamide

lUPAC name: (RS)-/\/,/\/-diethyl-2-(1-naphthyloxy)propionamide

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-14, is preferably in the range from 1 :2000 to 1 :2, in particular from 1 :800 to 1 :8, es pecially from 1 :400 to 1 :20, 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.

C-15. napropamide-M

lUPAC name: (R)-/\/,/\/-diethyl-2-(1-naphthyloxy)propionamide

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-15, is preferably in the range from 1 :2000 to 1 :2, in particular from 1 :800 to 1 :8, es pecially from 1 :400 to 1 :20, 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. C-16. pendimethalin

CAS name: A/-(1-ethylpropyl)-3,4-dimethyl-2,6-dinitrobenzenamine

In the combinations of the present invention, 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.

C-17. pethoxamid

CAS name: 2-chloro-/\/-(2-ethoxyethyl)-/\/-(2-methyl-1 -phenyl-1 -propenyl)acetamide

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-17, 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-17 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-17 are preferably ap plied 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.

C-18. picloram

lUPAC name: 4-amino-3,5,6-trichloropyridine-2-carboxylic acid.

Exemplary agriculturally acceptable salts or esters of picloram include picloram- dimethylammonium, picloram-2-ethylhexyl, picloram-isoctyl, picloram-methyl, picloram- hexyloxypropylammonium, picloram-olamine, picloram-potassium, picloram-triethylammonium, picloram-tris(2-hydroxypropyl)ammonium, picloram-trolamine, and mixtures thereof

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-18, is preferably in the range from 1 :20 to 20:1 , in particular from 1 :10 to 10:1 , es pecially from 1 :5 to 5:1 , wherein the herbicide A is calculated as the free acid form of imazamox and wherein the herbicide compound C-18 is calculated as the free acid. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-18 are preferably ap plied 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.

C-19. propaquizafop

lUPAC name: 2-isopropylideneaminooxyethyl (R)-2-[4-(6-chloroquinoxalin-2- yloxy)phenoxy]propionate. In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-19, is preferably in the range from 1 : 100 to 4:1 , in particular from 1 :50 to 2: 1 , espe cially from 1 :20 to 1 : 1 , wherein the herbicide A is calculated as the free acid form of imazamox 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 applied 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.

C-20. propisochlor

lUPAC name: 2-chloro-6'-ethyl-/\/-isopropoxymethylaceto-o-toluidide

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-20, 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-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.

C-21. propyzamide

lUPAC name: 3,5-dichloro-/\/-(1 , 1-dimethylpropynyl)benzamide

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-21 , 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-21 is calculated as such. Accordingly, in the methods and uses of the invention, the herbicide A and the herbicide C-21 are preferably ap plied 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.

C-22. pyroxasulfone

lUPAC name: 3-[5-(difluoromethoxy)-1-methyl-3-(trifluoromethyl)-1 /-/-pyrazol-4- ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1 ,2-oxazole

In the combinations of the present invention, 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 such. Accordingly, in the meth ods 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. C-23. quizalofop

lUPAC name: (RS)-2-[4-(6-chloroquinoxalin-2-yloxy)phenoxy]propionic acid.

Exemplary agriculturally acceptable salts or esters of quizalofop include quizalofop-ethyl.

In the combinations of the present invention, 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.

C-24. quizalofop-P

lUPAC name: (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.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-24, 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-24 is calculated as the free acid. Accordingly, in the methods 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.

C-25. 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid

(CAS 1628702-28-2) or an agriculturally acceptable salt or ester thereof.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the herbicide C-25, is preferably in the range from 1 :50 to 50:1 , in particular from 1 :20 to 20:1 , es pecially from 1 : 5 to 10:1 , wherein the herbicide A is calculated as the free acid form of imaza- mox and wherein the herbicide compound C-25 is calculated as the free acid. Accordingly, in the methods 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.

In the combinations of the present invention, the relative weight ratio of the herbicide A to the total amount of the herbicide B and the herbicide C is preferably from 1 :200 to 1 :1 , in particular from 1 :150 to 1 :2, especially 1 :100 to 1 :3, wherein the herbicides A and B are calculated as the respective free acid forms, and the herbicide C is calculated as the free acid or as such. Accord ingly, 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.

Particular embodiments of the combinations according to the invention are the following combi nations 1 to 26:

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: quinmerac 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: quinmerac or a salt thereof;

Herbicide C: aminopyralid or a salt thereof.

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: quinmerac 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: quinmerac or a salt thereof;

Herbicide C: clethodim.

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: quinmerac or a salt thereof;

Herbicide C: clomazone.

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: quinmerac or a salt thereof;

Herbicide C: clopyralid or a salt thereof. 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: quinmerac or a salt thereof;

Herbicide C: cycloxydim.

Combination 8: 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: quinmerac or a salt thereof;

Herbicide C: dimethachlor.

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: quinmerac or a salt thereof;

Herbicide C: dimethenamid-P.

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: quinmerac or a salt thereof;

Herbicide C: ethametsulfuron or ethametsulfuron-methyl.

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: quinmerac 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: quinmerac 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: quinmerac or a salt thereof;

Herbicide C: haloxyfop-P 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: quinmerac or a salt thereof;

Herbicide C: metazachlor.

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: quinmerac or a salt thereof;

Herbicide C: napropamide.

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: quinmerac or a salt thereof;

Herbicide C: napropamide-M.

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: quinmerac or a salt thereof;

Herbicide C: pendimethalin.

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: quinmerac or a salt thereof;

Herbicide C: pethoxamid.

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: quinmerac or a salt thereof;

Herbicide C: picloram or a salt or ester thereof.

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: quinmerac or a salt thereof;

Herbicide C: propaquizafop.

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: quinmerac or a salt thereof;

Herbicide C: propisochlor. 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: quinmerac or a salt thereof;

Herbicide C: propyzamide.

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: quinmerac or a salt thereof;

Herbicide C: pyroxasulfone.

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: quinmerac or a salt thereof;

Herbicide C: quizalofop 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: quinmerac or a salt thereof;

Herbicide C: quizalofop-P or an ester thereof.

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: quinmerac or a salt thereof;

Herbicide C: 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)-2- pyridinecarboxylic acid, or a salt or an ester thereof.

In Combinations 1 to 26, 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.

The 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.

According to one embodiment, the 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 family Poaceae (Gramineae), commonly known as grasses. According to a preferred embodiment, the compositions and methods of the present invention are suitable for controlling monocotyledonous weeds and crop volunteers, which are selected from the genera Alopecurus, Apera, Avena, Bromus, Hordeum, Lolium, Poa, and Triticum, in particular from the species Alopecurus myosuroides (ALOMY), Apera spica-venti (APESV), Av ena fatua (AVEFA), Bromus scoparius (BROSC), Bromus sterilis (BROST), Bromus tectorum (BROTE), Hordeum vulgare (HORVW, HORVS), Lolium multiflorum (LOLMU), Lolium rigidum (LOLRI), Poa annua (POAAN), Poa trivialis (POATR) and Triticum aestivum (TRZAW, TRZAS). According to a more preferred embodiment, the compositions and methods of the present in vention are suitable for controlling monocotyledonous weeds, which are selected from the gene ra Alopecurus, Apera, Bromus, Hordeum, Lolium, and Triticum, in particular from the species Alopecurus myosuroides (ALOMY), Apera spica-venti (APESV), Bromus scoparius (BROSC), Bromus sterilis (BROST), Bromus tectorum (BROTE), Hordeum vulgare (HORVW, HORVS), Lolium multiflorum (LOLMU), Lolium rigidum (LOLRI), and Triticum aestivum (TRZAW, TRZAS).

According to another embodiment, the compositions and methods of the present invention are suitable for controlling dicotyledonous weeds, commonly known as broadleaf weeds

According to a further preferred embodiment, the compositions and methods of the present in vention are suitable for controlling dicotyledonous weeds from the genera Ammi, Anthemis, Barbarea, Brassica, Bunias, Capsella, Centaurea, Chenopodium, Cirsium, Conium, Crepis, Daucus, Descurainia, Erigeron, Fumaria, Galium, Geranium, Lamium, Lycopsis, Matricaria, Mercurialis, Orobanche, Papaver, Polygonum, Raphanus, Senecio, Silene, Sinapis, Sonchus, Spergula, Sisymbrium, Stellaria, Thlaspi, Veronica, and Viola, and in particular from the species Ammi majus (AM IMA), Anthemis cotula (ANTCO), Anthemis arvensis (ANTAR), Barbarea vul garis (BARVU), Brassica napus (BRSNW, BRSNS), Bunias orientalis (BUNOR), Capsella bur- sa-pastoris (CAPBP), Chenopodium album (CHEAL), Cirsium arvense (CIRAR), Conium macu- latum (COIMA), Cyanus segetum (CENCY), Crepis capillaris (CVPCA), Daucus carota (DAU- CA), Descurainia sophia (DESSO), Erigeron bonariensis (ERIBO), Fumaria officinalis (FUMOF), Galium aparine (GALAP), Geranium dissectum (GERDI), Geranium pusillum (GERPU), Gerani um rotundifolium (GERRT), Lamium amplexicaule (LAMAM), Lamium purpureum (LAMPU), Lycopsis arvensis (LYCAR), Matricaria chamomilla (MATCH), Tripleurospermum inodorum (MATIN), Mercurialis annua (MERAN), Orobanche ramosa (ORARA), Papaver rhoeas

(PAPRH), Polygonum aviculare (POLAV), Fallopia convolvulus (POLCO), Polygonum lapathifo- lium (POLLA), Persicaria maculosa (POLPE), Raphanus raphanistrum (RAPRA), Senecio jaco- baea (SENJA), Senecio vulgaris (SENVU), Silene gallica (SILGA), Sinapis alba (SINAL), Sina pis arvensis (SINAR), Sonchus arvensis (SONAR), Sonchus oleraceus (SONOL), Spergula arvensis (SPRAR), Sisymbrium officinale (SSYOF), Stellaria media (STEME), Thlaspi arvense (THLAR), Veronica arvensis (VERAR), Veronica hederifolia (VERHE), Veronica persica

(VERPE), Veronica triphyllos (VERTR), and Viola arvensis (VIOAR). According to another embodiment, the compositions and methods of the present invention are suitable for controlling monocotyledonous and dicotyledonous weeds from the genera Alopecu- rus, Ammi, Anthemis, Apera, Avena, Barbarea, Brassica, Bromus, Bunias, Capsella, Centaurea, Chenopodium, Conium, Crepis, Daucus, Descurainia, Erigeron, Fumaria, Galium, Geranium, Hordeum, Lamium, Lolium, Lycopsis, Matricaria, Mercurialis, Orobanche, Papaver, Poa, Polyg onum, Raphanus, Senecio, Silene, Sinapis, Sonchus, Spergula, Sisymbrium, Stellaria, Thlaspi, Triticum, Veronica, and Viola.

According to another preferred embodiment, the compositions and methods of the present in vention are suitable for controlling monocotyledonous and dicotyledonous weeds in oilseed rape wherein the weeds are selected from the genera Alopecurus, Ammi, Anthemis, Apera, Barbar ea, Brassica, Bromus, Bunias, Capsella, Centaurea, Chenopodium, Conium, Daucus, Des curainia, Fumaria, Galium, Geranium, Hordeum, Lamium, Lolium, Lycopsis, Matricaria, Mercuri alis, Orobanche, Papaver, Raphanus, Sinapis, Sisymbrium, Stellaria, Thlaspi, Triticum, Veroni ca, and Viola, in particular from the genera Alopecurus, Ammi, Barbarea, Brassica, Capsella, Centaurea, Descurainia, Galium, Geranium, Hordeum, Lamium, Matricaria, Orobanche, Papa ver, Raphanus, Sinapsis, Sisymbrium, Stellaria, Thlaspi, Triticum, Veronica, and Viola, and very particular from the species Alopecurus myosuroides (ALOMY), Ammi majus (AMIMA), Barbarea vulgaris (BARVU), Brassica napus (BRSNW, BRSNS), Capsella bursa-pastoris (CAPBP), Cen taurea cyanus (CENCY), Descurainia sophia (DESSO), Galium aparine (GALAP), Geranium dissectum (GERDI), Geranium molle (GERMO), Geranium pusillum (GERPU), Geranium rotun- difolium (GERRT), Hordeum vulgare (HORVU), Lamium amplexicaule (LAMAM), Lamium pur- pureum (LAMPU), Matricaria chamomilla (MATCH), Matricaria inodora (MATIN), Orobanche ramosa (ORARA), Papaver rhoeas (PAPRH), Raphanus raphanistrum (RAPRA), Sinapis arvensis (SINAR), Sisymbrium officinale (SSYOF), Stellaria media (STEME), Thlaspi arvense (THLAR), Triticum aestivum (TRZAW), Veronica hederifolia (VERHE), Veronica persica

(VERPE), and Viola arvensis (VIOAR).

According to another embodiment, the 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.

They are considered weeds, which compete with the planted crop for moisture, nutrients and light. According to a further preferred embodiment, the 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). According to another embodiment, the compositions and methods of the present invention are useful for controlling monocotyledonous weeds and dicotyledonous weeds from the genera Alo- pecurus, Apera, Avena, Poa, Anthemis, Capsella, Centaurea, Descurainia, Galium, Matricaria, Papaver, Raphanus, Sinapis, Sisymbrium, Thlaspi, and Veronica, and in particular for control ling the monocotyledonous and dicotyledonous species Alopecurus myosuroides (ALOMY), Apera spica-venti (APESV), Avena fatua (AVEFA), Poa annua (POAAN), Anthemis arvensis (ANTAR), Capsella bursa-pastoris (CAPBP), Cyanus segetum (CENCY), Descurainia sophia (DESSO), Galium aparine (GALAP), Matricaria chamomilla (MATCH), Tripleurospermum ino- dorum (MATIN), Papaver rhoeas (PAPRH), Raphanus raphanistrum (RAPRA), Sinapis arvensis (SINAR), Sisymbrium officinale (SSYOF), Thlaspi arvense (THLAR), Veronica arvensis (VER- AR)Veronica hederifolia (VERHE), Veronica persica (VERPE), and Veronica triphyllos

(VERTR).

According to another embodiment, the compositions and methods of the present invention are useful for controlling monocotyledonous weeds and dicotyledonous weeds from the genera An themis, Crepis, Polygonum, Raphanus, Silene, Spergula, Sisymbrium, Veronica, and Viola, and in particular for controlling the monocotyledonous and dicotyledonous species Anthemis cotula (ANTCO), Anthemis arvensis (ANTAR), Crepis capillaris (CVPCA), Polygonum aviculare (PO- LAV), Fallopia convolvulus (POLCO), Persicaria maculosa (POLPE), Raphanus raphanistrum (RAPRA), Silene gallica (SILGA), Spergula arvensis (SPRAR), Sisymbrium officinale (SSYOF), Veronica persica (VERPE), and Viola arvensis (VIOAR).

According to another embodiment, the compositions and methods of the present invention are useful for controlling monocotyledonous weeds and dicotyledonous weeds from the genera Lo- lium, Erigeron, Polygonum, Raphanus, and Sonchus, and in particular for controlling the mono cotyledonous and dicotyledonous species Lolium rigidum (LOLRI), Erigeron bonariensis (ERI- BO), Polygonum aviculare (POLAV), Fallopia convolvulus (POLCO), Raphanus raphanistrum (RAPRA), and Sonchus oleraceus (SONOL).

According to another embodiment, the 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 hibitors (HRAC Group G), glutamine synthetase inhibitors (HRAC Group H), DHP synthase in hibitors (HRAC Group I), inhibitors of microtubuli assembly (HRAC Group K1), inhibitors of mi tosis/m icrotubuli organization (HRAC Group K2), very long chain fatty acid (VLCFA) inhibitors (HRAC Group K3), Inhibitors of cell wall synthesis (HRAC Group L), uncoupler (membran dis ruption) (HRAC Group M), Inhibitors of lipid synthesis (HRAC Group N), synthetic auxins (HRAC Group O), auxin transport inhibitors (HRAC Group P) and herbicides with unknown mode of action (HRAC Group Z).

Preferably, 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 L) and inhibitors of lipid synthesis (HRAC Group N).

More preferably, 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).

In particular, 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).

In another embodiment, 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, Conyza, Descurainia, Galium, Geranium, Kochia, Matricaria, Papaver, Polygonum, Raphanus, Sinapis, Sisymbrium, Stellaria and Thlaspi.

Preferably, the resistant or tolerant biotype is selected from the genera Agropyron, Alopecurus, Apera, Avena, Brachiaria, Bromus, Cynodon, Digitaria, Echinochloa, Eleusine, Ischaemum, Leptochloa, Lolium, Panicum, Phalaris, Poa, Rottboellia, Setaria, Anthemis, Amaranthus, Am brosia, Capsella, Centaurea, Chenopodium, Conyza, Descurainia, Galium, Kochia, Matricaria, Papaver, Raphanus, Sinapis, Sisymbrium, Stellaria and Thlaspi.

More preferably, the resistant or tolerant biotype is selected from the genera Alopecurus, Apera, Digitaria, Echinochloa, Leptochloa, Lolium, Phalaris, Poa, Setaria, Amaranthus, Anthemis, Capsella, Centaurea, Chenopodium, Descurania, Kochia, Matricaria, Papaver, Sisymbrium, Stellaria and Thlaspi, still more preferably selected from the genera Alopecurus, Apera, Echi nochloa, Leptochloa, Lolium, Phalaris, Poa, Amaranthus, Chenopodium, Matricaria, Papaver and Stellaria, even more preferably selected from the genera Alopecurus, Echinochloa, Lolium, Phalaris, Poa, Amaranthus, Chenopodium, Matricaria, Papaver and Stellaria, yet more prefera bly selected from the genera Alopecurus, Echinochloa, Lolium, Phalaris, Poa and Papaver and in particular selected from the genera Alopecurus, Lolium, Phalaris and Papaver.

In another embodiment, 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 nochloa, 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, Phalaris and Papaver.

In another embodiment, 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 lentils, 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 particularly suita ble for combating/controlling undesired vegetation in ALS tolerant oilseed rape (canola).

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® canola.

The combinations of the invention are particularly useful for combating/controlling undesired vegetation in in the following crops:

a. Brassica napus containing the CLB-1 AHASL trait having two substitutions, an A122(Af)T substitution and an S653(Af)N substitution.

b. Brassica napus containing the CL PM1 PM2 AHASL trait having two substitutions, an S653(Af)N substitution and an W574(Af)L substitution.

c. Brassica napus containing both the CLB-1 trait and one or two additional AHASL trait(s) that each have substitution(s) at at least one of the positions A122(Af), P197(Af), R199(Af), T203(Af), A205 (At), W574(Af), S653 (At), or G654 (At). d. Brassica napus containing both the CL PM1 PM2 trait and one or two additional AHASL trait(s) that each have substitution(s) at at least one of the positions A122(Af), P197(Af), R199(Af), T203(Af), A205 (At), W574(Af), S653 (At), or G654(Af). e. Brassica napus containing an AHASL trait having one A122(Af)T substitution.

If not stated otherwise, 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 biosyn thesis inhibitors, such as acetylCoA carboxylase (ACCase) inhibitors; or oxynil (i. 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. These 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, 1 185; 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. g., imazamox, or Ex- pressSun® sunflowers (DuPont, USA) being tolerant to sulfonyl ureas, e. g., tribenuron. Genetic engineering methods have been used to render cultivated plants, such as soybean, cotton, corn, beets and rape, tolerant to herbicides, such as glyphosate, imidazolinones and

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).

The combinations according to the invention can also be used in genetically modified crop plants. The term "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. Often, 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. Typically, 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. g., 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; ion channel blockers, such as blockers of sodium or calcium channels; juvenile hormone esterase; diuretic hormone recep tors (helicokinin receptors); stilbene synthase, bibenzyl synthase, chitinases or glucanases. In the context of the present invention, 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. These 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. g., described in the publi cations mentioned above, and some of which are commercially available, such as YieldGard® (corn cultivars producing the CrylAb toxin), YieldGard® Plus (corn cultivars producing CrylAb and Cry3Bb1 toxins), Starlink® (corn cultivars producing the Cry9c toxin), Herculex® RW (corn cultivars producing Cry34Ab1 , Cry35Ab1 and the enzyme Phosphinothricin-N-Acetyltransferase [PAT]); NuCOTN® 33B (cotton cultivars producing the Cry1 Ac toxin), Bollgard® I (cotton culti vars producing the CrylAc toxin), Bollgard® II (cotton cultivars producing CrylAc and Cry2Ab2 toxins); VIPCOT® (cotton cultivars producing a VIP-toxin); NewLeaf® (potato cultivars produc ing the Cry3A toxin); Bt-Xtra®, NatureGard®, KnockOut®, BiteGard®, Protecta®, Bt1 1 (e. g., Agrisure® CB) and Bt176 from Syngenta Seeds SAS, France, (corn cultivars producing the CrylAb toxin and PAT enzyme), MIR604 from Syngenta Seeds SAS, France (corn cultivars producing a modified version of the Cry3A toxin, c.f. WO 03/018810), MON 863 from Monsanto Europe S.A., Belgium (corn cultivars producing the Cry3Bb1 toxin), IPC 531 from Monsanto Europe S.A., Belgium (cotton cultivars producing a modified version of the CrylAc toxin) and 1507 from Pioneer Overseas Corporation, Belgium (corn cultivars producing the Cry1 F toxin and PAT enzyme).

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. Examples of such proteins are the so-called“pathogenesis-related proteins” (PR proteins, see, e.g., EP-A 392 225), plant disease resistance genes (e. g., 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). The methods for producing such genetically modified plants are generally known to the person skilled in the art and are described, e.g., in the publications mentioned above.

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.

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. When the combinations are used in crops, they can be applied after seeding and before or after the emergence of the crop plants. The compositions invention can, however, also be applied prior to seeding of the crop plants.

It is a particular benefit of the combinations according to the invention that they have a very good post-emergence herbicide activity, i.e. they show a good herbicidal activity against emerged undesirable plants. Thus, in a preferred embodiment of invention, 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.

In any case, the herbicide A, the herbicide B, and the optional herbicide C can be applied simul taneously or in succession.

In a preferred embodiment, 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. Preferably, 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.

It is also possible to apply several compositions successively, where compositions contain only one or two herbicide compounds selected from the herbicide A, the herbicide B, and the option al herbicide C, provided that the compositions together comprise the herbicide A, the herbicide B, and the optional herbicide C.

The 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.

In the case of a post-emergence treatment of the plants, 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.

In the method of the invention, the application rate of the herbicide A, calculated as the free acid of imazamox, is generally from 1 to 200 g/ha and in particular from 2 to 100 g/ha or from 5 to 50 g/ha.

In the method of the invention, the application rate of the herbicide B, calculated as the free acid of quinmerac, is generally from 10 to 2500 g/ha, in particular from 50 to 1500 g/ha, preferably from 50 to 500 g/ha. If the herbicide C is aminopyralid, the application rate of aminopyralid (calculated as the free acid) is in the range from 1 to 250 g/ha, preferably in the range from 2 to 50 g/ha.

If the herbicide C is bixlozone, the application rate of bixlozone (calculated as such) is in the range from 20 to 1000 g/ha, preferably in the range from 40 to 500 g/ha.

If the herbicide C is clethodim, the application rate of clethodim (calculated as such) is in the range from 20 to 500 g/ha, preferably in the range from 60 to 250 g/ha.

If the herbicide C is clomazone, the application rate of clomazone (calculated as such) is in the range from 20 to 1000 g/ha, preferably in the range from 40 to 500 g/ha.

If the herbicide C is clopyralid, the application rate of clopyralid (calculated as the free acid) is in the range from 20 to 1000 g/ha, preferably in the range from 50 to 500 g/ha.

If the herbicide C is cycloxydim, the application rate of cycloxydim (calculated as such) is in the range from 20 to 2000 g/ha, preferably in the range from 50 to 750 g/ha.

If the herbicide C is dimethachlor, the application rate of dimethachlor (calculated as such) is in the range from 200 to 2500 g/ha, preferably in the range from 500 to 2000 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 2500 g/ha, preferably in the range from 300 to 1500 g/ha.

If the herbicide C is ethametsulfuron or ethametsulfuron-methyl, the application rate of ethamet- sulfuron (calculated as the free acid) is preferably in the range from 5 to 100 g/ha.

If the herbicide C is fluazifop-P, 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.

If the herbicide C is halauxifen, 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.

If the herbicide C is haloxyfop-P, the application rate of haloxyfop -P (calculated as the free ac id) is in the range from 5 to 500 g/ha, preferably in the range from 10 to 300 g/ha.

If the herbicide C is metazachlor, the application rate of metazachlor (calculated as such) is in the range from 200 to 2000 g/ha, preferably in the range from 400 to 1500 g/ha. If the herbicide C is napropamide, the application rate of napropamide (calculated as such) is in the range from 500 to 5000 g/ha, preferably in the range from 750 to 2000 g/ha.

If the herbicide C is napropamide-M, the application rate of napropamide-M (calculated as such) is in the range from 500 to 5000 g/ha, preferably in the range from 750 to 2000 g/ha.

If the herbicide C is pendimethalin, the application rate of pendimethalin (calculated as such) is in the range from 250 to 2500 g/ha, preferably in the range from 500 to 2000 g/ha.

If the herbicide C is pethoxamid, the application rate of pethoxamid (calculated as such) is in the range from 500 to 5000 g/ha, preferably in the range from 750 to 2000 g/ha.

If the herbicide C is picloram, the application rate of picloram (calculated as the free acid) is in the range from 5 to 250 g/ha, preferably in the range from 10 to 100 g/ha.

If the herbicide C is propaquizafop, 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.

If the herbicide C is propisochlor, the application rate of propisochlor (calculated as such) is in the range from 200 to 5000 g/ha, preferably in the range from 500 to 3000 g/ha.

If the herbicide C is propyzamide, the application rate of propyzamide (calculated as such) is in the range from 100 to 2500 g/ha, preferably in the range from 200 to 1500 g/ha.

If the herbicide C is pyroxasulfone, the application rate of pyroxasulfone (calculated as such) is in the range from 10 to 500 g/ha, preferably in the range from 25 to 250 g/ha.

If the herbicide C is quizalofop, 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 20 to 200 g/ha.

If the herbicide C is quizalofop-P, 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 20 to 200 g/ha.

If the herbicide C is 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid (CAS 1628702-28-2), the application rate of 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1 H-indol- 6-yl)-2-pyridinecarboxylic acid (calculated as the free acid) is preferably in the range from 1 to 100 g/ha. The present invention also relates to compositions and formulations comprising a combination according to the present invention.

The compositions usually contain, besides the combinations of the invention, at least one formulation additive. Generally, 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.

The 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®.

Particularly suitable adjuvants comprise a polar solvent and a phosphate ester of the formula (A)

R¹ 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, and

wherein the 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. 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. 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. In the case of two or three package formulations the two or three formulations are preferably mixed prior to application. Preferably, the mixing is performed as a tank mix, i.e. the formulations are mixed immediately prior or upon dilution with water.

In the formulations of the present invention, the active ingredients, i.e. the herbicides A, B, and optionally C, 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.

Depending on 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. The person skilled in the art is sufficiently familiar with the recipes for such formulations. 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.

Suitable surfactants (adjuvants, wetting agents, tackifiers, dispersants and also emulsifiers) are the alkali metal salts, alkaline earth metal salts and ammonium salts of aromatic sulfonic acids, for example lignosulfonic acids (e.g. Borrespers-types, Borregaard), phenolsulfonic acids, naphthalenesulfonic acids (Morwet types, Akzo Nobel) and dibutylnaphthalenesulfonic acid (Nekal types, BASF SE), and of fatty acids, alkyl- and alkylarylsulfonates, alkyl sulfates, lauryl ether sulfates and fatty alcohol sulfates, and salts of sulfated hexa-, hepta- and octadecanols, and also of fatty alcohol glycol ethers, condensates of sulfonated naphthalene and its derivatives with formaldehyde, condensates of naphthalene or of the naphthalenesulfonic acids with phenol and formaldehyde, polyoxyethylene octylphenol ether, ethoxylated isooctyl-, octyl- or nonylphenol, alkylphenyl or tributylphenyl polyglycol ether, alkylaryl polyether alcohols, isotridecyl alcohol, fatty alcohol/ethylene oxide condensates, ethoxylated castor oil,

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.

Examples of 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) are

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 Engelhardt). Examples of antifoams are 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. Examples of 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).

Examples of antifreeze agents are ethylene glycol, propylene glycol, urea or glycerol.

Examples of 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.

Examples of adhesives are polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose.

To prepare emulsions, pastes or oil dispersions, the active the components, as such or dis solved in an oil or solvent, can be homogenized in water by means of wetting agent, tackifier, dispersant or emulsifier. Alternatively, it is possible to prepare 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. The concentrations of the active ingredients in the formulations can be varied within wide ranges. In general, 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).

The active herbicide compounds A and B as well as the compositions according to the invention can, for example, be formulated as follows:

1. Products for dilution with water

A Water-soluble concentrates

10 parts by weight of the herbicides A, B, and optionally C, are dissolved in 90 parts by weight of water or a water-soluble solvent. As an alternative, wetters or other adjuvants are added. The active compound dissolves upon dilution with water. This gives a formulation with an active compound content of 10% by weight.

B Dispersible concentrates

20 parts by weight of the herbicides A, B, and optionally C, are dissolved in 70 parts by weight of cyclohexanone with addition of 10 parts by weight of a dispersant, for example

polyvinylpyrrolidone. Dilution with water gives a dispersion. The active compound content is 20% by weight.

2. C Emulsifiable concentrates

15 parts by weight of the herbicides A, B, and optionally C, are dissolved in 75 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). Dilution with water gives an emulsion. The formulation has an active compound content of 15% by weight.

D Emulsions

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). 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.

E Suspensions In an agitated ball mill, 20 parts by weight of 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.

F Water-dispersible granules and water-soluble granules

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.

G Water-dispersible powders and water-soluble powders

75 parts by weight of 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.

H Gel formulations

In a ball mill, 20 parts by weight of the herbicides A, B, and optionally C, 10 parts by weight of dispersant, 1 part by weight of gelling agent and 70 parts by weight of water or of an organic solvent are mixed to give a fine suspension. Dilution with water gives a stable suspension with active compound content of 20% by weight.

2. Products to be applied undiluted

3. I Dusts

5 parts by weight of the herbicides A, B, and optionally C, are ground finely and mixed intimately with 95 parts by weight of finely divided kaolin. This gives a dusting powder with an active compound content of 5% by weight.

4. J Granules (GR, FG, GG, MG)

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. K ULV solutions (UL)

10 parts by weight of the herbicides A, B, and optionally C, are dissolved in 90 parts by weight of an organic solvent, for example xylene. This gives a product to be applied undiluted with an active compound content of 10% by weight.

Aqueous use forms can be prepared from emulsion concentrates, suspensions, pastes, wetta- ble powders or water-dispersible granules by adding water.

It may, furthermore, be beneficial to apply the 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. Also of interest is the 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.

USE EXAMPLES:

The effect of the herbicidal combinations according to the invention on the growth of undesira ble plants compared to the herbicidal active compounds alone was demonstrated by the follow ing greenhouse experiments.

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.

For the pre-emergence and post-emergence treatments, 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. In all use examples, plants were grown in a greenhouse environment.

The containers were irrigated gently to promote germination and growth. For the post emergence treatment, the 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.

Depending on the species, 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.

Beyond^® herbicide: 120g/l SL formulation of imazamox as racemate (rac)

Gavelan: 50% WP quinmerac

R-imazamox: tech material, 120 g/l SL formulation

Runway VA: 30 g/l SL aminopyralid

DAT : days after treatment 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. Here, 0 means no damage and 100 means complete destruction of the plants. (X*) in the tables below represents the expected value according to Colby. The plants used in the greenhouse experiments belonged to the following species:

Colby's formulae were applied to determine whether the composition showed synergistic action: S. R. Colby (1967)“Calculating synergistic and antagonistic responses of herbicide combina- tions", Weeds 15, p. 22 ff.

E = X + Y - (CΎ/100) (I) where in formula I

X = effect in percent using herbicide A + B at an application rate a or a+b, respectively; Y = effect in percent using herbicide C at application rate c, respectively E = expected effect (in %) of A + B + C at application rates a + b + c.

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.

Crop selectivity

Table 1 :

Table 2:

Efficacy

Table 3

imazamox (rac) R-imazamox quinmerac 19 DAT: Damage [%],

[g/ha] [g/ha] [g/ha] AMARE POLCO

1.56 15.625 85 60

1.56 15.625 95 75

Table 4

Table 5

imazamox (rac) R-imazamox quinmerac 19 DAT: Damage [%],

Table 6

Table 7

Table 8

imazamox R-imazamox quinmerac 19 DAT: Damage [%],

Table 9

Table 10

Table 11

Table 12

Table 13

Table 14

Table 14

Table 15

[g/ha] 20 DAT: Damage [%],

SETFA

imazamox (rac) 4 95

R-imazamox 2.8 95

quinmerac 62.5 0

imazamox (rac) + quinmerac 4+62.5 95

R-imazamox + quinmerac 2.8+62.5 98 (95*)

Table 16

[g/ha] 20 DAT: Damage [%],

SETFA

imazamox (rac) 2 90

R-imazamox 1.4 90

quinmerac + aminopyralid 62.5+1 0

imazamox (rac) + quinmerac + aminopyralid 2+62.5+1 90

R-imazamox + quinmerac + aminopyralid 1.4+62.5+1 95 (90*) Table 17

Table 18

Claims

Claims

1. The use of herbicidally active combinations consisting of herbicides A, B, and optionally C, for the selective control of undesirable vegetation in cultures of crop plants, wherein a. the herbicide A is R-imazamox, any non-racemic mixture of R-lmazamox and S- Imazamox, wherein the proportion of R-lmazamox is at least 80% by weight, or an ag riculturally acceptable salt or ester thereof; and

b. the herbicide B is quinmerac, or an agriculturally acceptable salt or ester thereof; and c. the optional herbicide C is selected from the group consisting of aminopyralid,

bixlozone, clethodim, clomazone, clopyralid, cycloxydim, dimethachlor, DMTA-p, ethametsulfuron, fluazifop-P, halauxifen, haloxyfop-P, metazachlor, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, propisochlor, propyzamide, pyroxasulfone, quizalofop, quizalofop-P, 4-amino-3-chloro-5-fluoro-6-(7- fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid, and the salts and esters thereof;

and wherein the crop plant is selected from imidazolinone tolerant crops.

2. The use according to claim 1 , wherein the imidazolinone tolerant crop is selected from oilseed rape and canola.

3. The use according to claim 1 or 2, wherein the combination consists of herbicides A and B.

4. The use according to any one of claims 1 to 3, wherein the relative weight ratio of the herbicide A and the herbicide B is in the range from 1 :20 to 1 :5.

5. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is aminopyralid, a salt or ester thereof.

6. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is bixlozone.

7. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is clopyralid, a salt or ester thereof.

8. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is dimethachlor.

9. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is DMTA-p.

10. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is halauxifen, a salt or ester thereof.

11. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is metazachlor.

12. The use according to claim 1 or 2, wherein the combination consists of herbicides A, B and C, wherein C is picloram, a salt or ester thereof.

13. The use according to any of the preceding claims, wherein the undesirable vegetation is selected from the genera Alopecurus, Ammi, Anthemis, Apera, Avena, Barbarea, Brassi- ca, Bromus, Bunias, Capsella, Centaurea, Chenopodium, Conium, Crepis, Daucus, Des- curainia, Erigeron, Fumaria, Galium, Geranium, Hordeum, Lamium, Lolium, Lycopsis, Matricaria, Mercurialis, Orobanche, Papaver, Poa, Polygonum, Raphanus, Senecio, Sile- ne, Sinapis, Sonchus, Spergula, Sisymbrium, Stellaria, Thlaspi, Triticum, Veronica, and Viola.

14. The use according to any of the preceding claims, wherein the undesirable vegetation comprises volunteer crop selected from the genera Brassica, Hordeum, and Triticum.

15. The use according to any of the preceding claims, wherein the undesirable vegetation comprises herbicide resistant species.

16. Herbicidally active combinations consisting of herbicides A, B, and optionally C, wherein a. the herbicide A is R-imazamox, any non-racemic mixture of R-lmazamox and S- Imazamox, wherein the proportion of R-lmazamox is at least 80% by weight, or an ag riculturally acceptable salt or ester thereof; and

b. the herbicide B is quinmerac, or an agriculturally acceptable salt or ester thereof; and c. the optional herbicide C is selected from the group consisting of aminopyralid,

bixlozone, clethodim, clomazone, clopyralid, cycloxydim, dimethachlor, DMTA-p, ethametsulfuron, fluazifop-P, halauxifen, haloxyfop-P, metazachlor, napropamide, napropamide-M, pendimethalin, pethoxamid, picloram, propaquizafop, propisochlor, propyzamide, pyroxasulfone, quizalofop, quizalofop-P, 4-amino-3-chloro-5-fluoro-6-(7- fluoro-1 H-indol-6-yl)-2-pyridinecarboxylic acid and the salts and esters thereof.

17. The combination according to claim 16, wherein the combination consists of herbicides A and B.

18. The combination according to claim 16 or 17, wherein the relative weight ratio of the herb icide A and the herbicide B is in the range from 1 :20 to 1 :5.

19. Herbicidally active compositions comprising a combination as claimed in any one of

claims 16 to 18 and one or more auxiliaries customary in crop protection.

20. The composition according to claim 19, comprising an adjuvant which comprises a polar solvent and a phosphate ester of the formula (A)

O

R^a_ii_R^b (A)

0 H in which

R¹ 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, and

wherein the 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;

and optionally and one or more further formulation auxiliaries.

21. A method for controlling undesirable vegetation which comprises applying to the vegeta tion or the locus thereof or applying to the soil or water to prevent the emergence or growth of the undesirable vegetation the combinations or composition as claimed in any one of claims 16 to 20.