| Title of Invention | HERBICIDAL COMPOSITIONS COMPRISING PYROXASULFONE IV |
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| Abstract | The present invention relates to herbicidally active compositions, which comprise 3-[5-(difluoromethoxy)-1- methyl-3-(trifluoromethyl)pyrazol-4-ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole [common name pyroxasulfone] and at least one herbicide B and at least one herbicide compound B which is an selected from inhibitors of the very long chain fatty acids (VLCFA) synthesis. The invention furthermore relates to the use of a composition as defined herein for controlling undesirable vegetation, in particular in crops. When using the compositions of the invention for this purpose the herbicide A and the at least one herbicide B can be applied simultaneously or in succession, where undesirable vegetation may occur. |
| Full Text | Herbicidal compositions comprising pyroxasulfone IV The present invention relates to herbicidally active compositions, which comprise 3-[5- (difiuoromethoxy)-1-methyl-3-(trifluoromethyl)pyrazol-4-ylmethyisulfonyi]-4,5-dihydro- 5,5-dimethyl-1,2-oxazole [common name pyroxasulfone] and at least one herbicide B. Background of the invention In crop protection, it is desirable in principle to increase the specificity and the reliability of the action of active compounds. In particular, it is desirable for the crop protection product to control the harmful plants effectively and, at the same time, to be tolerated by the useful plants in question. Pyroxasulfone has been described in EP-A 1364946 and US 2005/0256004. Although pyroxasulfone is a highly effective pre-emergence herbicide, its activity at low application rates is not always satisfactory. Moreover, pyroxasulfone is known to have only poor post-emergence activity (Y. Yamaji et al., "Application timing and field per- formance of KlH-485", Conference Abstract l-1-ii-12B of 11. IUPAC International Con- gress of Pesticide Chemistry, 2006 Kobe, Japan). Apart from that, its compatibility with certain dicotyledonous crop plants, such as cotton, sunflower, soybean, brassica crops, such as canola and oilseed rape, and some gramineous crops such as rice, wheat, rye and barley is not always satisfactory, i.e. in addition to the harmful plants, the crop plants are also damaged to an extent which is not acceptable. Though it is In principle possible to spare crop plants by lowering the application rates, the extent of the control of harmful plants is naturally also reduced. It is known that combined application of certain different herbicides with specific action might result in an enhanced activity of a herbicide component in comparison with a simple additive action. Such an enhanced activity is also termed a synergism or syner- gistic activity. As a consequence, it is possible to reduce the application rates of herbi- cidally active compounds required for controlling the harmful plants. WO 2005/104848 describes compositions containing a herbicidal 3-sulfonylisoxazoline compounds such as pyroxasulfone and a herbicide-antagonistically active amount of a safener. Similar compositions are known from WO 2007/006509. US 2005/256004, for example, discloses that in a pre-emergence treatment, joint appli- cation of certain herbicidal 3-sulfonylisoxazoline compounds such as pyroxasulfone with atrazine or cyanazine results in an increased overall herbicide action against cer- tain monocotyledonous and dicotyledonous annual broadleaf weeds (lambsquarter, green foxtail, veivetleaf) in comparison with a simple expected additive action. WO 2006/097322 discloses a herbicidal composition comprising pyroxasulfone and a second herbicide selected from tembotrione, topramezone and 4-hydroxy-3-[[2-[(2- methoxyethoxy)methyl]-6-{trifluoromethyl-3-pyridinyl]carbonyl]bicyclo[3.2.1]oct-3-ene-2- one. WO 2006/097509 discloses a herbicidal composition comprising a herbicidal 3- sulfonylisoxazoline compound such as pyroxasulfone and a phenyluracil compound. Unfortunately, it is usually not possible to predict synergistic activity for combinations of known herbicides, even if the compounds show a close structural similarity to known synergistic combinations. Summary of the invention It is an object of the present invention to provide herbicidal compositions, which show enhanced herbicide action in comparison with the herbicide action of pyroxasulfone against undesirable harmful plants, in particular against Alopecurus myosuroides, Avena fatua, Bromus spec, Echinocloa spec. Lolium spec, Phalaris spec, Setaria spec, Digitaria spec, Brachiaria spec, Amaranthus spec, Chenopodium spec, Abuti- lon theophrasti, Galium aparine, Veronica spec, or Solanum spec and/or to improve their compatibility with crop plants, in particular improved compatibility with wheat, bar- ley, rye, rice, soybean, sunflower, brassica crops and/or cotton. The composition should also have a good herbicidal activity in post-emergence applications. The com- positions should also show an accelerated action on harmful plants, i.e. they should effect damaging of the harmful plants more quickly in comparison with application of the individual herbicides. We have found that this object is achieved, surprisingly, by herbicidally active composi- tions comprising a) pyroxasulfone, i.e. 3-[5-(difluoromethoxy)-1-methyl-3-(trifiuoromethyl)pyrazol-4- ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole (hereinafter also referred to as herbicide A); and b) at least one herbicide compound B which is an selected from inhibitors of the very long chain fatty acids (VLCFA) synthesis. The invention relates in particular to compositions in the form of herbicidally active compositions as defined above. The invention furthermore relates to the use of a composition as defined herein for con- trolling undesirable vegetation, in particular in crops. When using the compositions of the invention for this purpose the herbicide A and the at least one herbicide B can be applied simultaneously or in succession, where undesirable vegetation may occur. The invention furthermore relates to the use of a composition as defined herein for con- trolling undesirable vegetation in crops which, by genetic engineering or by breeding, are resistant or tolerant to one or more herbicides and/or pathogens such as plant- pathogenous fungi, and/or to attack by insects; preferably resistant or tolerant to one or more herbicides that act as VLCFA synthesis inhibitors. The invention furthermore relates to a method for controlling undesirable vegetation, which comprises applying an herbicidal composition according to the present invention to the undesirable plants. Application can be done before, during and/or after, prefera- bly during and/or after, the emergence of the undesirable plants. The herbicide A and the at least one herbicide B can be applied simultaneously or in succession. 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 composition according to the present invention to act on plants, their habitat or on seed. In the uses and methods of the present invention it is immaterial whether the herbicide A and the at least one herbicide B are formulated and applied jointly or separately, and, in the case of separate application, in which order the application takes place. It is only necessary, that the herbicide A and the at least one herbicide B are applied in a time frame, which allows simultaneous action of the active ingredients on the plants. The invention also relates to a herbicide formulation, which comprises a herbicidally active composition as defined herein and at least one carrier material, including liquid and/or solid carrier materials. Detailed description of the invention Surprisingly, the compositions according to the 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 pyroxasulfone and the at least one herbicide B results in an enhanced activity against harmful plants in the sense of a synergy effect (synergism). For this reason, the compositions can, based on the indi- vidual components, be used at lower application rates to achieve a herbicidal effect comparable to the individual components. Moreover, the compositions of the present invention provide good post-emergence herbicidal activity, i.e. the compositions are particularly useful for combating/controlling harmful plants after their emergence. Apart form that, the compositions of the present invention show good crop compatibility, i.e. their use in crops leads to a reduced damage of the crop plants and/or does not result in increased damage of the crop plants. As used herein, the terms "controlling" and "combating" are synonyms. As used herein, the terms "undesirable vegetation" and "harmful plants" are synonyms. The compositions of the invention comprise pyroxasulfone as a first component a). As a second component b), the compositions of the invention comprise at least one herbicide B which is an inhibitor of the VLCFA synthesis (VLCFA inhibitor). VLCFA inhibitors are compounds which have a mode of action comprising the inhibition of the VLCA synthesis and/or the inhibition of cell division in plants and which belong to the group K3 of the HRAC classification system (see HRAC, Classification of Herbicides According to Mode of Action, http://www.plantprotection.org/hrac/MOA.html). VLCFA inhibitors include e.g. chloroacetamide herbicides, such as acetochlor, alachlor, butachlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, S- metolachlor, pethoxamid, pretilachlor, propachlor, propisochlor and thenylchlor, oxya- cetamide heribicides, such as flufenacet and mefenacet, acetamide herbicides, such as as diphenamid, napropamide and naproanilide, tetrazolinone herbicides, such as fen- trazamide as well as herbicides not belonging to a common group, such as anilofos, cafenstrole and piperophos. The term "VLCFA inhibitor" is meant herein to also include the respective salts, isomers and esters of the above mentioned compounds. Suitable salts are e.g. salts of alkaline or earth alkaline metals or ammonium or organoammo- nium salts, for instance, sodium, pottasium, ammonium, isopropyl ammonium etc. Suit- able isomers are e.g. stereo isomers such as the enantiomers. Suitable esters are e.g. C1-C8-(branched or non-branched) alkyl esters, such as methylesters, ethylesters, iso propyl esters. Preferred VLCFA inhibitors according to the present invention are selected from the group consisting of chloroacetamide herbicides, in particular acetochlor, dimethachior, dimethenamid, dimethenamid-P, metazachlor, propisochlor, pethoxamide, metolachlor, and metolachlor-S and oxyacetamide herbicides, in particular flufenacet. In the compositions of the present invention the relative weight ratio of pyroxasulfone to herbicide B is preferably in the range from 1:250 to 250:1, in particular in the range of 1:200 to 200:1 and more preferably from 150:1 to 1:150. Accordingly, in the methods and uses of the invention, pyroxasulfone and the at least one herbicide B are applied within these weight ratios. The compositions of the invention may also comprise, as a component c), one or more safeners. Safeners, also termed as herbicide safeners, are organic compounds which in some cases lead to better crop plant compatibility when applied jointly with specifi- cally acting herbicides. Some safeners are themselves herbicidally active. In these cases, the safeners act as antidote or antagonist in the crop plants and thus reduce or even prevent damage to the crop plants. However, in the compositions of the present invention, safeners are generally not required. Therefore, a preferred embodiment of the invention relates to compositions which contain no safener or virtually no safener (i.e. less than 1 % by weight, based on the total amount of herbicide A and herbicide B). Suitable safeners, which can be used in the compositions according to the present in- vention, are known in the art, e.g. from The Compendium of Pesticide Common Names (http://www.alanwood.net/pesticides/); Farm Chemicals Handbook 2000 Vol. 86, Meister Publishing Company, 2000; B. Hock, C. Fedtke, R. R. Schmidt, Herbizide, Georg Thieme Verlag, Stuttgart 1995; W. H. Ahrens, Herbicide Handbook, 7th Edition, Weed Science Society of America, 1994; and K. K. Hatzios, Herbicide Handbook, Supplement to 7th Edition, Weed Science Society of America, 1998. Safeners include e.g. benoxacor, cloquintocet, cyometrinil, cyprosulfamide, dichlormid, dicyclonon, dietholate, fenchlorazole, fenclorim, flurazole, fluxofenim, furilazole, isoxadifen, mefenpyr, mephenate, naphthalic anhydride, 2,2,5-trimethyl-3- (dichloracetyl)-1 ,3-oxazolidine, 4-(dichloroacetyl)-1-oxa-4-azaspiro[4.5]decane and oxabetrinil, as well as thereof agriculturally acceptable salts and, provided they have a carboxyl group, their agriculturally acceptable derivatives. 2,2,5-Trimethyl-3- (dichloroacetyl)-1,3-cxazolidine [CAS No. 52836-31-4] is also known under the name R-29148.4-(Dichloroacetyl)-1-oxa-4- azaspiro[4.5]decane [CAS No. 71526-07-03] is also known under the names AD-67 and MON 4660. As a safener, the compositions according to the invention particularly preferably com- prise at least one of the compounds selected from the group of benoxacor, cloquinto- cet, cyprosulfamide, dichlormid, fenchlorazole, fenclorim, fluxofenim, furilazole, isoxadifen, mefenpyr, naphthalic anhydride, 2,2,5-trimethyl-3-(dichioroacetyl)-1,3- oxazolidine, and 4-(dlchloroacetyi)-1-oxa-4-azaspiro[4.5]decane and oxabetrinil; and the agriculturally acceptable salt thereof and, in the case of compounds having a COOH group, an agriculturally acceptable derivative as defined below. A preferred embodiment of the invention relates to compositions which contain no safener or virtually no safener (i.e. less than 1 % by weight, based on the total amount of herbicide A and the at least one herbicide B is applied). The compositions of the invention may also comprise, as a component d), one or more herbicides D which are different from the herbicides A and B. Such further herbicides D may broaden the activity spectrum of the inventive compositions. However, further herbicides D are generally not required. Therefore, a preferred embodiment of the in- vention relates to compositions which contain no further herbicide D or virtually no fur- ther herbicide D (i.e. less than 1 % by weight, based on the total amount of herbicide A and herbicide B). Another embodiment of the invention however relates to compositions which contain a herbicide D selected from the group consisting of quinmerac, salts of quinmerac and clomazone. A similar embodiment of the invention relates to compositions which con- tain a herbicide D selected from the group consisting of aminopyralid and the salts thereof. In particular, the compositions of the present invention consist of the herbicide A and the at least one herbicide B, i.e. they neither contain a safener nor a further herbicide D other than quinmerac, salts of quinmerac, aminopyralid, salts of aminopyralid and clo- mazone. If compositions of the present invention contain clomazone or quinmerac, the relative weight ratio of clomazone, aminopyralid or quinmerac to herbicide B is preferably in the range from 1:200 to 200:1, in particular in the range of 1:100 to 100:1 and more pref- erably from 1:50 to 50:1. The weight ratio of pyroxasuifone to the total amount of herbi- cide B + clomazone or quinmerac is then preferably from 1:500 to 250:1, in particular in the range of 1:250 to 100:1 and more preferably from 1:200 to 50:1. A further embodiment of the invention relates to compositions which additionally com- prise a herbicide D selected from the group consisting of imidazolinone herbicides and their mixtures with quinmerac, aminopyralid or their salts or clomazone. In the em- bodiment, the composition of the present invention preferably consists of herbicide A, the at least one herbicide B, and the further herbicide D which is selected from imida- zolinone herbicides, i.e. they neither contain a safener nor a further herbicide D other than an imidazolinone herbicide, quinmerac, aminopyralid or a salt thereof or cloma- zone. Imidazolinone herbicides include e.g. imazapic, imazamethabenz, imazamox, ima- zapyr, imazaquin, and imazethapyr and the salts thereof and in case of imazametha- benz the esters thereof such as imazamethabenz-methyl. Preferred imidazolinone her- bicides are selected from imazapic, imazamox and the salts and esters thereof. In the compositions of this particular embodiment the relative weight ratio of pyroxasul- fone to imidazolinone herbicide D is preferably in the range from 1:500 to 500:1, in par- ticular in the range from 1:250 to 250:1 and more preferably from 100:1 to 1:100. Ac- cordingly, in the methods and uses of the invention, pyroxasulfone and the imidazoli- none herbicide are applied within these weight ratios. Another embodiment of the invention relates to compositions which additionally com- prise at least one further herbicide D which is selected from herbicides that are inhibi- tors of the photosystem II, which are also termed as PS-II inhibitors or ETP inhibitors. PS-II inhibitors are compounds, which have a mode of action comprising the inhibition of the electron transfer in photosystem II of the photosynthesis in plants and which be- long to the groups C1 to C3 of the HRAC classification system (see HRAC, Classifica- tion of Herbicides According to Mode of Action, http://www.plantprotection.org/hrac/MOA.html). In this embodiment, the composition of the present invention preferably consists of herbicide A, the at least one herbicide B, and the further herbicide D which is selected from PS-II inhibitor herbicides, i.e. they neither contain a safener nor a further herbicide D other than a herbicide of the group of PS-II inhibitors. Preferably, the PS-II inhibitors are selected from the group consisting of: d.1 arylurea herbicides; d.2 triazin(di)one herbicides; d.3 methylthiotriazine herbicides; and d.4 chlorotriazine herbicides. Arylurea herbicides (d.1) include e.g. chlorbromuron, chlorotoiuron, chloroxuron, dimefuron, diuron, ethidimuron, fenuron, fluometuron, isoproturon, isuron, linuron, methabenzthiazuron, metobromuron, metoxuron, monolinuron, neburon, siduron, tetrafluron and thebuthiuron. Preferred arylurea herbicides herbicides (d.1) include chlortoluron, diuron, linuron, isoproturon and tebuthiuron, with particular preference given to diuron and tebuthiuron. Triazin(di)one herbicides (d.2) include e.g. ametridione, amibuzin, hexazinone, isomethiozin, metamitron and metribuzin. Preferred triazin(di)one herbicides (d.2) in- clude hexazinone and metribuzin. Methylthiotriazine herbicides (d.3) include e.g. ametryn, aziprotryne, cyanatryn, desmetryn, dimethametryn, methoprotryne, prometryn, simetryn and terbutryn. Pre- ferred methylthiotriazine herbicide is ametryn. Chlorotriazine herbicides (d.4) include e.g. atrazine, chlorazin, cyanazin, cyprazine, propazin, simazin, terbuthylazine and trietazine. Preferred chlorotriazine herbicide is atrazine and terbuthylazine. Arylurea herbicides (group d.1), triazin(di)one heribicides (group d.2), methylthiotriazine herbicides (group d.3) and chlorotriazine herbicides (group d.3)are known e.g. from K.- W. Munks and K.-H. Müller "Photosynthesis Inhibitors" in "Modem Crop Protection Compounds" Vol. 1, Wiley-VHC 2007, pp 359-400; C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), and also from The Compendium of Pesticide Common Names, http://www.alanwood.net/pesticides/. In the compositions of this particular embodiment the relative weight ratio of pyroxasul- fone to PS-II inhibitor herbicide D is preferably in the range from 1:500 to 500:1, in par- ticular in the range from 1:250 to 250:1 and more preferably from 100:1 to 1:100. Ac- cordingly, in the methods and uses of the invention, pyroxasulfone and the herbicide D are applied within these weight ratios. Another embodiment of the invention relates to compositions which additionally com- prise at least one further herbicide D which is selected from herbicides that are inhibi- tors of the 4-hydroxyphenylpyruvate dioxygenase, which are also termed as HPPD inhibitors. HPPD inhibitors are herbicide compounds, which have a mode of action comprising the inhibition of the 4-hydroxyphenylpyruvate dioxygenase in plants and which belong to the group F2 of the HRAC classification system (see HRAC, Classifi- cation of Herbicides According to IVIode of Action, http://www.plantprotection.org/hrac/MOA.html). In this embodiment, the composition of the present invention preferably consists of herbicide A, the at least one herbicide B, and the further herbicide D which is selected from HPPD inhibitor herbicides, i.e. they neither contain a safener nor a further herbicide D other than a herbicide of the group of HPPD inhibitors. HPPD inhibitor herbicides include e.g. isoxafiutole, sulcotrione, mesotrione, tem- botrione, topramezone, and the salts thereof. In this embodiment compositions are preferred, where the HPPD inhibitor herbicide is topramezone or a salt thereof. In the compositions of this particular embodiment the relative weight ratio of pyroxasul- fone to HPPD inhibitor herbicide D is preferably in the range from 1:100 to 100:1, in particular in the range from 1: 50 to 50:1. Accordingly, in the methods and uses of the invention, pyroxasulfone and the herbicide D are applied within these weight ratios. in yet a further embodiment of the invention, the composition may additionally comprise nicosulfuron, if the herbicide B is dimethenamid or dimethenamid-P. In the composi- tions of this particular embodiment the relative weight ratio of pyroxasulfone to nicosul- furon is preferably in the range from 1:100 to 100:1, in particular in the range from 1: 50 to 50:1. If the compounds of herbicide compounds mentioned as herbicides B, herbicides D and safeners (see below) have functional groups, which can be ionized, they can also be used in the form of their agriculturally acceptable salts. In general, the salts of those cations are suitable whose cations have no adverse effect on the action of the active compounds ("agricultural acceptable"). In general, the salts of those cations are suitable whose cations have no adverse effect on the action of the active compounds ("agricultural acceptable"). Preferred cations are the ions of the alkali metals, preferably of lithium, sodium and potassium, of the alkaline earth metals, preferably of calcium and magnesium, and of the transition metals, pref- erably of manganese, copper, zinc and iron, furthermore ammonium and substituted ammonium (hereinafter also termed as organoammonium) in which one to four hydro- gen atoms are replaced by C1-C4-alkyl, hydroxy-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, hydroxy-C1-C4-alkoxy-C1-C4-alkyl, phenyl or benzyl, preferably ammonium, methylam- monium, isopropylammonium, dimethylammonium, diisopropylammonium, trimethyl- ammonium, tetramethylammonium, tetraethylammonium, tetrabutylammonlum, 2- hydroxyethylammonium, 2-(2-hydroxyethoxy)eth-1-yiammonium (diglycolamine salts), di(2-hydroxyeth-1-yl)ammonium (diolamine salts), tris((2-hydroxyeth-1-yl)ammonium (trolamine salts), tris(3-propanol)amonium, benzyltrimethylammonium, benzyltriethyl- ammonium, furthermore phosphonium ions, sulfonium ions, preferably tri(C1-C4- alkyl)sulfonium such as trimethylsulfonium, and sulfoxonium ions, preferably tri(C1-C4- alkyl)sulfoxonium. In the compositions according to the invention, the compounds that carry a carboxyl group can also be employed in the form of agriculturally acceptable derivatives, for example as amides such as mono- or di-C1-C6-alkylamides or arylamides, as esters, for example as allyl esters, propargyl esters, C1-C10-alkyl esters or alkoxyalkyl esters, and also as thioesters, for example as C1-C10-alkyl thioesters. Preferred mono- and di- C1-C6-alkylamides are the methyl- and the dimethylamides. Preferred arylamides are, for example, the anilidines and the 2-chloroanilides. Preferred alkyl esters are, for ex- ample, the methyl, ethyl, propyl, isopropyl, butyl, isobutyl, pentyl, mexyl (1-methylhexyl) or isooctyl (2-ethylhexyl) esters. Preferred C1-C4-alkoxy-C1-C4-alkyl esters are the straight-chain or branched C1-C4-alkoxyethyl esters, for example the methoxyethyl, ethoxyethyl or butoxyethyl esters. An example of the straight-chain or branched C1-C10- alkyl thioesters is the ethyl thioester. Preferred derivatives are the esters. The compositions of the present invention are suitable for controlling a large number of harmful plants, including monocotyledonous weeds, in particular annual weeds such as gramineous weeds (grasses) including Echinochloa species such as bamyardgrass (Echinochloa crusgalli var. crus-galli), Digitaria species such as crabgrass (Digitaria sanguinalis), Setaria species such as green foxtail (Setaria viridis) and giant foxtail (Se- taria faberii). Sorghum species such as johnsongrass (Sorghum halepense Pers.), Avena species such as wild oats (Avena fatua), Cenchrus species such as Cenchrus echinatus, Bromus species, Lolium species, Phalaris species, Eriochloa species, Pani- cum species, Brachiaria species, annual bluegrass (Poa annua), blackgrass (Alopecu- rus myosuroides), Aegilops cylindrica, Agropyron repens, Apera spica-venti, Eleusine indica, Cynodon dactylon and the like. The compositions of the present invention are also suitable for controlling a large num- ber of dicotyledonous weeds, in particular broad leaf weeds including Polygonum spe- cies such as wild buckwheat (Polygonum convolvolus), Amaranthus species such as pigweed (Amaranthus retroflexus), Chenopodium species such as common lambsquar- ters (Chenopodium album L), Sida species such as prickly sida (Sida spinosa L.), Am- brosia species such as common ragweed (Ambrosia artemisiifolia), Acanthospermum species, Anthemis species, Atriplex species, Cirsium species, Convolvulus species, Conyza species, Cassia species, Commelina species. Datura species, Euphorbia spe- cies, Geranium species, Galinsoga species, morningglory (Ipomoea species), Lamium species, Malva species, IVIatricaria species, Sysimbrium species, Solanum species, Xanthium species, Veronica species, Viola species, common chiclcweed (Steliaria me- dia), veivetleaf (Abutilon theophrasti), Hemp sesbania (Sesbania exaltata Cory), Anoda cristata, Bidens pilosa, Brassica kaber, Capsella bursa-pastoris, Centaurea cyanus, Gaieopsis tetrahit, Galium aparine, Helianthus annuus, Desmodium tortuosum, Kochia scoparia, Mercurialis annua, Myosotis arvensis, Papaver rhoeas, Raphanus raphanis- trum, Salsola kali, Sinapis arvensis, Sonchus arvensis, Thlaspi arvense, Tagetes minuta, Richardia brasiliensis, and the like. The compositions of the present invention are also suitable for controlling a large num- ber of annual and perennial sedge weeds including cyperus species such as purple nutsedge (Cyperus rotundus L.), yellow nutsedge (Cyperus esculentus L.), hime-kugu (Cyperus brevifolius H.), sedge weed (Cyperus microiria Steud), rice flatsedge (Cype- rus iria L.), and the like. The compositions according to the present invention are suitable for combat- ing/controlling common harmful plants in useful plants (i.e. in crops). The compositions of the present invention are generally suitable for combating/controlling undesired vegetation in - Grain crops, including e.g. - cereals (small grain cereals) such as wheat (Triticum aestivum) and wheat like crops such as durum (T. durum), einkom (T. monococcum), emmer (T. dicoccon) and spelt (T. spelta), rye (Secale cereale), triticale (Tritiosecale), barley (Hordeum vulgare); - maize (com; Zea mays); - sorghum (e.g. Sorghum bicoloui); - rice (Oryza spp. such as Oryza sativa and Oryza glaberrima); and - sugar cane; - Legumes (Fabaceae), including e.g. soybeans (Glycine max.), peanuts (Arachis hypogaea and pulse crops such as peas including Pisum sativum, pigeon pea and cowpea, beans including broad beans (Vicia faba), Vigna spp., and Phaseo- lus spp. and lentils (lens culinaris van); - brassicaceae, including e.g. canola (Brassica napus), oilseed rape (Brassica napus), cabbage (S. oleracea van), mustard such as B.juncea, B. campestris, B. narinosa, B. nigra and B. tournefortii; and turnip (Brassica rapa var.); - other broadleaf crops including e.g. sunflower, cotton, flax, linseed, sugarbeet, potato and tomato; - TNV-crops (TNV: trees, nuts and vine) including e.g. grapes, citrus, pomefruit, e.g. apple and pear, coffee, pistachio and oilpalm, stonefruit, e.g. peach, almond, walnut, olive, cherry, plum and apricot; - turf, pasture and rangeland; - onion and garlic; - bulb ornamentals such as tulips and narcissus; - garden ornamentals such as roses, petunia, marigold, snap dragon; and - conifers and deciduous trees such as pinus, fir, oak, maple, dogwood, haw- thorne, crabapple, and rhamnus (buckthorn). The compositions of the present invention are in particular suitable for combat- ing/controlling undesired vegetation in wheat, barley, rye, triticale, durum, rice, corn, sugarcane, sorghum, soybean, pulse crops such as pea, bean and lentils, peanut, sun- flower, sugarbeet, potato, cotton, brassica crops, such as oilseed rape, canola, mus- tard, cabbage and turnip, turf, grapes, pomefruit, such as apple and pear, stonefruit, such as peach, almond, walnut, olive, cherry, plum and apricot citrus, coffee, pistachio, garden ornamentals, such as roses, petunia, marigold, snap dragon, bulb ornamentals such as tulips and narcissus, conifers and deciduous trees such as pinus, fir, oak, ma- ple, dogwood, hawthome, crabapple and rhamnus. The compositions of the present invention are most suitable for combating/controlling undesired vegetation in wheat, barley, rye, triticale, durum, rice, com, sugarcane, sor- ghum, soybean, pulse crops such as pea, bean and lentils, peanut, sunflower, sugarbeet, potato, cotton, brassica crops, such as oilseed rape, canola, mustard, cab- bage and tumip, turf, grapes, stonefruit, such as peach, almond, walnut, olive, cherry, plum and apricot, citrus and pistachio. If not stated otherwise, the compositions of the invention are suitable for application in any variety of the aforementioned crop plants. The compositions of the invention are particularly suitable for application in wheat, bar- ley, rye, corn, sugarcane, sorghum, soybean, pulse crops, sunflower, sugarbeet, po- tato, brassica crops and turf. The compositions according to the invention can also be used in crop plants which are resistant or tolerant to one or more herbicides owing to genetic engineering or breed- ing, which are resistant or tolerant to one or more pathogens owing to genetic engi- neering or breeding, or which are resistant or tolerant to attack by insects owing to ge- netic engineering or breeding. Suitable are for example crop plants, preferably corn, wheat, sorghum, bariey, sunflower, rice, canola, oilseed rape, soybeans or lentils which are resistant or tolerant to herbicidal VLCA inhibitors, such as, for example, acetochlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, propisochlor, pethox- amide, metolachlor, metolachlor-S or flufenacet, orcrop plants which, owing to intro- duction of the gene for Bt toxin by genetic modification, are resistant to attack by cer- tain insects. The compositions of the present invention can be applied in conventional manner by using techniques a skilled person is familiar with. Suitable techniques include spraying, atomizing, dusting, spreading or watering. The type of application depends on the in- tended purpose in a well known manner; in any case, the technique should ensure the finest possible distribution of the active ingredients according to the invention. The compositions can be applied pre- or post-emergence, i.e. before, during and/or after emergence of the undesirable plants. When the compositions are used in crops, they can be applied after seeding and before 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 compositions 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 compositions are applied post-emergence, i.e. during and/or after the emergence of the undesirable plants. It is particularly advantageous to apply the mixtures according to the invention post-emergent when the undesirable plant starts with leaf development of up to 6 leaves. Since the composition show good crop tolerance, even when the crop has already emerged, they can be applied after seeding of the crop plants and in par- ticular during or after the emergence of the crop plants. In any case herbicide A and the at least one herbicide B and the optional further ac- tives (safener C and herbicide D) can be applied simultaneously or in succession. The compositions are applied to the plants mainly by spraying, in particular foliar spray- ing. Application can be carried out by customary spraying techniques using, for exam- ple, water as carrier and spray liquor rates of from about 10 to 2000 I/ha or 50 to 1000 I/ha (for example from 100 to 500 I/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. If the active ingredients are less well tolerated by certain crop plants, application tech- niques may be used in which the herbicidal compositions are sprayed, with the aid of the spray apparatus, in such a way that they come into as little contact, if any, with the leaves of the sensitive crop plants while reaching the leaves of undesirable plants, which grow underneath, or the bare soil (post-directed, lay-by). 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 effected, for example, by usual spraying techniques with water as the carrier, using amounts of spray mixture of approx. 50 to 1000 I/ha. The required application rate of the composition of the pure active compounds, i.e. of pyroxasulfone, herbicide B and optionally safener or herbicide D depends on the den- sity of the undesired vegetation, on the development stage of the plants, on the climatic conditions of the location where the composition is used and on the application method. In general, the application rate of the composition (total amount of pyroxasul- fone, herbicide B and optional further actives) is from 15 to 6000 g/ha, frequently from 15 to 5000 g/ha, preferably from 20 to 2500 g/ha of active substance. The required application rates of pyroxasulfone are generally in the range from 1 g/ha to 500 g/ha and preferably in the range from 5 g/ha to 400 g/ha or from 10 g/ha to 300 g/ha of active substance. The required application rates of the herbicide B (total amount of herbicide B) are gen- erally in the range from 1 g/ha to 5000 g/ha and preferably in the range from 5 g/ha to 4000 g/ha or from 10 g/ha to 3000 g/ha of active substance. The required application rates of the safener, if applied, are generally in the range from 1 g/ha to 5000 g/ha and preferably in the range from 2 g/ha to 5000 g/ha or from 5 g/ha to 5000 g/ha of active substance. Preferably no safener or virtually no safener is ap- plied and thus the application rates are below 5 g/ha, in particular below 2 g/ha or be- low 1 g/ha. The required application rates of the further herbicide D, if applied, depends from the nature of the herbicide D and may generally be in the range from 0.1 g/ha to 5000 g/ha and preferably in the range from 0.1 g/ha to 5000 g/ha or from 1 g/ha to 5000 g/ha of active substance. In case of nicosulfuron, the application rate is generally in the range of 0.1 to 200 g/ha, preferably from 1 to 150 g/ha, in particular from 2 to 100 g/ha of active substance. In case of imidazolinone herbicides, the application rate is generally in the range of 0.1 to 500 g/ha, preferably from 1 to 250 g/ha, in particular from 2 to 200 g/ha of active substance. In case of PS-II inhibitor herbicides, the application rate is generally in the range of 1 g/ha to 5000 g/ha and preferably in the range from 5 g/ha to 4000 g/ha or from 10 g/ha to 3000 g/ha of active substance. In case of HPPD inhibitor herbicides, the application rate is generally in the range of 1 g/ha to 1000 g/ha and preferably in the range from 5 g/ha to 750 g/ha or from 10 g/ha to 500 g/ha of active substance. According to a first embodiment of the invention, the component b) comprises at least one chloroacetamide herbicide. Chloroacetamide herbicides are known from e.g. C.D.S. Tomlin, The Pesticide Manual", 13th Edition, BCPC (2003), and also from The Compendium of Pesticide Common Names, http://www.alanwood.net/pesticides/. Chloroacetamide herbicides include acetochlor, alachlor, butachlor, butenachlor, delachlor, diethatyl, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, meto- lachlor, S-metolachlor, pethoxamide, pretilachlor, propachlor, propisochlor, prynachlor, terbuchlor, thenylchlor and xylachlor, their salts, in particular their sodium salts, potas- sium salts, ammonium salts or substituted ammonium salts as defined above, their isomers, in particular their enantiomers, and their esters, in particular their C1-C8-alkyl esters, such as methylesters, ethylesters, iso propyl esters. Suitable examples of such esters include diethatyl-ethyl. Preferred chloroacetamide herbicides include acetochlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, S-metolachlor, pethoxamide and propi- sochlor, their salts and their esters, as well as mixtures thereof, in particular acetochlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor and propisochlor, their salts, their isomers and their esters, as well as mixtures thereof. In particular preferred compositions of this embodiment, the herbicide B comprises or in particular is acetochlor. In other particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is dimethachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is dimethenamid. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is dimethenamid-P. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is metazachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is propisochlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of dimethenamid or dimethenamid-P and meta- zachlor. In these particular preferred compositions the weight ratio of dimethenamid (or dimethenamid-P) to metazachlor is from 100:1 to 1:100, in particular from 1:50 to 50:1. In further preferred compositions of this embodiment, the composition comprise, in ad- dition to the herbicide B, quinmerac or a salt thereof or clomazone. Thus, these com- position may be regarded as comprising as a herbicide B or bing as a herbicide B a mixture of quinmerac or a salt thereof or clomazone and at least one chloroacetamide herbicide. In these preferred compositions the chloroacetamide herbicide is preferably selected from acetochlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, metolachlor, S-metolachlor, pethoxamide and propisochlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of quinmerac or a salt thereof and metazachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or In particular is a mixture of clomazone and metazachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular Is a mixture of quinmerac or a salt thereof and dimethenamid or dimethenamid-P. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of clomazone and dimethenamid or dimethenamid-P. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of quinmerac or a salt thereof and dimethachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of clomazone and dimethachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of quinmerac or a salt thereof and pethoxamid. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of clomazone and pethoxamid. In further preferred compositions of this embodiment, the herbicide B comprises or in particular is a mixture of aminopyralid or a salt thereof and at least one chloroacetamide herbicide. In these preferred compositions the chloroacetamide herbi- cide is preferably selected from acetochlor, dimethachlor, dimethenamid, dimethena- mid-P, metazachlor, metolachlor, S-metolachlor, pethoxamide and propisochlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of aminopyralid or a salt thereof and metazachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of aminopyrallid or a salt thereof and dimethenamid or dimethenamid-P. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of aminopyralid or a salt thereof and dimethachlor. In further particular preferred compositions of this embodiment, the herbicide B com- prises or in particular is a mixture of aminopyralid or a salt thereof and pethoxamid. In a further prefered composition of this embodiment, the herbicide B comprises or in particular is dimethenamid or dimethenamid P, the composition further comprising nicosulfuoron. In this embodiment the relative weight ratio of pyroxasulfone and herbicide B is pref- erably from 250:1 to 1:250 and more preferably from 100:1 to 1:100. The rate of application of pyroxasulfone is usually from 1 g/ha to 500 g/ha and prefera- bly in the range from 5 g/ha to 400 g/ha or from 10 g/ha to 300 g/ha of active substance (a.s.). The rate of application of the chloroacetamide herbicides is usually 1 to 5000 g/ha, as a rule 5 to 4000 g/ha, preferably 10 to 3000 g/ha, of active substance (a.s.). If present, the rate of application of quinmerac is usually 1 to 1500 g/ha, as a rule 5 to 1000 g/ha, preferably 10 to 750 g/ha, of active substance (a.s.). If present, the rate of application of clomazone is usually 1 to 2000 g/ha, as a rule 5 to 1500 g/ha, preferably 10 to 1000 g/ha, of active substance (a.s.). If present, the rate of application of aminopyralid is usually 1 to 1500 g/ha, as a rule 5 to 1000 g/ha, preferably 10 to 750 g/ha, of active substance (a.s.). If present, the rate of application of nicosulfuron is usually 0,1 to 200 g/ha, as a mle 1 to 150 g/ha, preferably 2 to 100 g/ha, of active substance (a.s.). If compositions of this embodiment contain clomazone, aminopyralid or quinmerac, the relative weight ratio of clomazone, aminopyralid or quinmerac to chloroacetamide her- bicide is preferably in the range from 1:200 to 200:1, in particular in the range of 1:100 to 100:1 and more preferably from 1:50 to 50:1. The weight ratio of pyroxasulfone to the total amount of chloroacetamide herbicide + clomazone, aminopyralid or quinmerac is then preferably from 1:500 to 250:1, in particular in the range of 1:250 to 100:1 and more preferably from 1:200 to 50:1. The compositions of this embodiment are particularly suitable for controlling mono- and dicotyledonous weeds and sedge weeds, in particular Alopecurus myosuroides, Apera spica-venti, Avena fatua, Brachiaria spec, Bromus spec., Cenchurs spec, Digitaria spec, Echinochloa spec, Eleusine indica, Eriochloa spec, Geranium spec, Lolium spec, Panicum spec, Phalaris spec, Poa annua, Setaria spec. Sorghum spec, Abuthilon theoprasti, Amaranthus spec, Atriplex spec, Brassica kaber, Capsella bursa-pastoris, Chenopodium spec, Conyza spec, Euphorbia spec, Galium aparine, Kochia scoparia. Polygonum spec, Raphanus raphanistrum, Sinapis arvensis, So- lanum spec, Sysimbrium spec, Thlaspi arvense, Commelina spec and Cyperus spec. The compositions of this embodiment are in particular suitable for combating undesired vegetation in wheat, barley, rye, triticale, durum, rice, com, sugarcane, sorghum, soy- bean, pulse crops such as pea, bean and lentils, peanut, sunflower, sugarbeet, potato, cotton, brassica crops, such as oilseed rape, canola, mustard, cabbage and turnip, turf, grapes, stonefruit, such as peach, almond, walnut, olive, cherry, plum and apricot, cit- rus and pistachio. If not stated otherwise, the compositions of this embodiment are suitable for application in any variety of the aforementioned crop plants. The compositions of this embodiment are particularly suitable for application in wheat, barley, corn, sugarcane, sorghum, soybean, pulse crops, peanut, sunflower, potato, cotton, brassica crops and turf. Compositions of the invention, which comprise a mixture of a chloroacetamide and a further herbicide, selected from quinmerac, a salt thereof, aminopyralid, a salt thereof and clomazone, can be used in the aforementioned crops. They are particularly useful for application in crops of oilseed rape, as they provide increased control of undesirable weeds at reduced application rates and thus at reduced risk of crop damage. Compositions of the invention, which comprise a mixture of metazachlor and di- methenamid or dimethenamid P can be used in the aforementioned crops. They are particularly useful for application in crops of oilseed rape, as they provide increased control of undesirable weeds at reduced application rates and thus at reduced risk of crop damage. Compositions of the invention, which comprise a mixture of dimethenamid or di- methenamid P and nicosulfuron can be used in the aforementioned crops. They are particularly useful for application in com, as they provide increased control of undesir- able weeds at reduced application rates and thus at reduced risk of crop damage. The compositions of this embodiment can preferably be used in crops which tolerate and/or are resistant to the action of VLCFA inhibitor herbicides, preferably in crops which tolerate and/or are resistant to the action of chloroacetamide herbicides. The resistance and or tolerance to said herbicides may be achieved by conventional breed- ing and/or by genetic engineering methods. As explained above, the compositions of the first embodiment may additionally com- prise a herbicide D selected from the group consisting of imidazolinone herbicides and their mixtures with quinmerac, aminopyralid or their salts or clomazone. Thus, the compositions of this particular embodiment (embodiment 1a) comprise or preferably consist of the herbicide A, the at least one herbicide B which is selected from the group of chloroacetamides and in particular from dimethenamid, dimethenamid-P and meta- zachlor, at least one imidazolinone herbicide, which is preferably selected from ima- zapic, imazamox and the salts and esters thereof such as imazapic-ammonium or ima- zamox-ammonium, and optionally a second herbicide, which is selected from quin- merac, aminopyralid or a salt thereof or clomazone. Particular preferred mixtures of the embodiment 1a are mixtures comprising or in par- ticular consisting of: Pyroxasulfone, dimethenamid or dimethenamid-P and imazapic or a salt or ester thereof (com position 1 a.1); Pyroxasulfone, metazachlor and imazamox or a salt or ester thereof (composition 1a.2);and Pyroxasulfone, metazachior, imazamox or a salt or ester thereof and quinmerac (com- position 1a.3); and The compositions 1a.1, 1a.2 and 1a.3 can be used in the aforementioned crops. The composition 1a.1 is particularly useful for application in crops of sugarcane, as it pro- vides increased control of undesirable weeds at reduced application rates and thus at reduced risk of crop damage. The compositions 1a.2 and 1a.3 are particularly useful for application in crops of oilseed rape and sunflowers, as they provide increased con- trol of undesirable weeds at reduced application rates and thus at reduced risk of crop damage. The compositions of the first embodiment may also additionally comprise a herbicide D, which is selected from herbicides that are inhibitors of the photosystem II. These com- positions are hereinafter also termed as compositions according to embodiment 1b. Thus, the compositions of this particular embodiment (embodiment 1 b) comprise or preferably consist of the herbicide A, the at least one herbicide B which is selected from the group of chloroacetamides and in particular from dimethenamid and di- methenamid-P and at least one PS-II inhibitor herbicide. The PS-II inhibitors in the compositions of the embodiment 1b are preferably selected from the group consisting of: d.1 arylurea herbicides, in particular the compounds mentioned as compounds of group d.1, which are preferably selected from chlortoluron, diuron, linuron, isoproturon and tebuthiuron, with particular preference given to diuron and tebuthiuron; d.2 triazin(di)one herbicides, in particular the compounds mentioned as compounds of group d.2, which are preferably selected from hexazinone and metribuzin; d.3 methylthiotriazine herbicides, in particular the compounds mentioned as com- pounds of group d.3, which are preferably the group consisting of ametryn; and d.4 chlorotriazine herbicides, in particular the compounds mentioned as compounds of group d.2, which are preferably selected from atrazine and terbuthylazine In particular preferred compositions of this embodiment 1b, the herbicide B comprises or in particular is dimethenamid or dimethenamid P. In particular preferred compositions of this embodiment 1lb, the herbicide D comprises or in particular is selected from the group consisting of diuron, metribuzin, ametryne, hexazinone and tebuthiuron. Examples of such compositions are: Composition 1b.1: pyroxasulfone + dimethenamid + diuron. Composition 1b.2: pyroxasulfone + dimethenamid + metribuzin, Composition 1b.3: pyroxasulfone + dimethenamid + ametryne, Composition 1b.4: pyroxasulfone + dimethenamid + hexazinone, Composition 1b.5: pyroxasulfone + dimethenamid + tebuthiurone. Composition 1b.6: pyroxasulfone + dimethenamid-P + diuron, Composition 1b.7: pyroxasulfone + dimethenamid-P + metribuzin, Composition 1b.8: pyroxasulfone + dimethenamid-P + ametryne, Composition 1b.9: pyroxasulfone + dimethenamid-P + hexazinone and Composition 1b.10: pyroxasulfone + dimethenamid-P + tebuthiurone. in further particular preferred compositions of this embodiment 1 b, the herbicide D comprises or in particular is selected from the group consisting of atrazine and ter- buthylazine. Examples of such compositions are: Composition 1b.11: pyroxasulfone + dimethenamid + atrazine and Composition 1b. 12: pyroxasulfone + dimethenamid + terbuthylazine Composition 1b.13: pyroxasulfone + dimethenamid-P + atrazine and Composition 1b.14: pyroxasulfone + dimethenamid-P + terbuthylazine The compositions of the embodiment 1b can be used for the same purpose as the compositions of embodiment 1. The compositions of the embodiment 1 b are particu- larly useful for application in crops, in particular in grain crops. They are especially use- ful for application in corn and sugarcane, as they provide increased control of undesir- able weeds at reduced application rates and thus at reduced risk of crop damage. Mix- tures 1b.1 to 1b.10 are especially useful for application in sugarcane, while mixtures 1 b.11 to 1 b.14 are particularly useful for application in corn. The compositions of the first embodiment may also additionally comprise a herbicide D, which is selected from herbicides that are HPPD inhibitors. These compositions are hereinafter also termed as compositions according to embodiment 1c. Thus, the com- positions of this particular embodiment (embodiment 1c) comprise or preferably consist of the herbicide A, the at least one herbicide B which is selected from the group of chloroacetamides and in particular from dimethenamid and dimethenamid-P and at least one HPPD inhibitor herbicide. The HPPD inhibitors in the compositions of the embodiment 1c are preferably selected from the group consisting of isoxaflutole, sulco- trione, mesotrione, tembotrione, topramezone, and the salts thereof. In this embodi- ment 1c compositions are preferred, where the HPPD inhibitor herbicide is toprame- zone or a salt thereof. In particular preferred compositions of this embodiment 1c, the herbicide B comprises or in particular is dimethenamid or dimethenamid P. In particular preferred composi- tions of this embodiment 1c, the herbicide D comprises or in particular is selected from the group consisting of topramezone and the salts thereof. Thus, a particular mixture of the embodiment 1 c comprises or in particular consists of pyroxasulfone, dimethenamid- P and topramezone or a salt thereof. The compositions of the embodiment 1c can be used for the same purpose as the compositions of embodiment 1. The compositions of the embodiment 1c are particu- lariy useful for application in crops. They are especially useful for application in oilseed rape, as they provide increased control of undesirable weeds at reduced application rates and thus at reduced risk of crop damage. According to a second embodiment of the invention, the component b) comprises at least one oxyacetamide herbicide. Oxyacetamide herbicides are known from e.g. G. Hamprecht et al. "Inhibition of Cell Division (Oxyacetamides, Tetrazolinones)" in "Mod- em Crop Protection Compounds" Vol. 1, Wiley-VHC 2007, pp 325-334; C.D.S. Tomlin, "The Pesticide Manual", 13th Edition, BCPC (2003), and also from The Compendium of Pesticide Common Names http.7/www.alanwood.net/pesticides/. Examples of suitable herbicides of this embodiment are mefenacet and flufenacet, and their salts, as well as mixtures thereof. In particularly preferred compositions of this embodiment, the herbicide B comprises or in particular is flufenacet. This compound is known e.g. from DE 3821600 (Bayer AG). In this embodiment the relative weight ratio of pyroxasulfone and herbicide B is fre- quently from 100:1 to 1:100, preferably from 50:1 to 1:50. The rate of application of pyroxasulfone is usually from 1 g/ha to 500 g/ha and prefera- bly in the range from 5 g/ha to 400 g/ha or from 10 g/ha to 300 g/ha of active substance (a.s.). The rate of application of the oxyacetamide herbicide is usually 1 to 1500 g/ha, as a rule 5 to 1000 g/ha, preferably 10 to 750 g/ha, of active substance (a.s.). The compositions of this embodiment are particularly suitable for controlling mono- and dicotyledonous weeds and sedge weeds, in particular Alopecurus myosuroides, Apera spica-venti, Avena fatua, Brachiaria spec, Bromus spec, Cenchrus spec, Digitaria spec, Echinochloa spec, Eleusine indica, Eriochloa spec, Loiium spec, Panicum spec, Phalaris spec, Poa annua, Setaria spec, Sorghum spec, Abuthilon theoprasti, Amaranthus spec, Chenopodium spec, Commelina spec, and Cyperus spec. The compositions of this embodiment are in particular suitable for combating undesired vegetation in in wheat, barley, rye, triticale, durum, rice, com, sugarcane, sorghum, soybean, pulse crops such as pea, bean and lentils, peanut, sunflower, sugarbeet, po- tato, cotton, brassica crops, such as oilseed rape, canola, mustard, cabbage and tur- nip, turf, grapes, stonefruit, such as peach, almond, walnut, olive, cherry, plum and apricot, citrus and pistachio. If not stated otherwise, the compositions of this embodiment are suitable for application in any variety of the aforementioned crop plants. The compositions of this embodiment are most suitable for application in wheat, barley, rye, triticale, durum, corn, soybeans, sugarcane, potato and cotton. The compositions of this embodiment can preferably be used in crops which tolerate and/or are resistant to the action of VLCFA inhibitor herbicides, preferably in crops which tolerate and/or are resistant to the action of oxyacetamide herbicides. The resis- tance and or tolerance to said herbicides may be achieved by conventional breeding and/or by genetic engineering methods. The present invention also relates to formulations of the compositions according to the present invention. The formulations contain, besides the composition, at least one organic or inorganic carrier material. The formulations may also contain, if desired, one or more surfactants and, if desired, one or more further auxiliaries customary for crop protection compositions. The formulation may be in the fonn of a single package formulation containing both the herbicide A and the at least one herbicide B together with liquid and/or solid carrier materials, and, if desired, 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 package formulation, wherein one package contains a formulation of py- roxasulfone while the other package contains a formulation of the at least one herbicide B and wherein both formulations contain at least one carrier material, if desired, one or more surfactants and, if desired, one or more further auxiliaries customary for crop pro- tection compositions. In the case of two package formulations the fomnulation contain- ing pyroxasulfone and the formulation containing the herbicide B are 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. If the composition comprises one or more further actives such as a safener C and/or a herbicide D, the composition may also be in the form of a three or four package formulation. In the formulation of the present invention the active ingredients, i.e. pyroxasulfone, herbicide B and optional further actives are present in suspended, emulsified or dis- solved form. The formulation according to the invention can be in the form of aqueous solutions, powders, suspensions, also highly-concentrated aqueous, oily or other sus- pensions or dispersions, aqueous emulsions, aqueous microemulsions, aqueous suspo-emulsions, oil dispersions, pastes, dusts, materials for spreading or granules. Depending on the formulation type, 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 inor- ganic 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 solvents such as cyclic and aromatic hydrocarbons, e.g. paraffins, tetrahy- dronaphthalene, alkylated naphthalenes and their derivatives, alkylated benzenes and their derivatives, alcohols such as methanol, ethanol, propanol, butanol and cyclohex- anol, ketones such as cydohexanone, strongly polar solvents, e.g. amines such as N- methylpyrrolidone, and water as well as mixtures 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 ammonium 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. 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 fomnulations. 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.I. Pigment Red 112 and C.I. 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 dissolved 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 emuisifier 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 a) and b) and optionally safener c) and/or herbi- cides D with a solid carrier. Granules, e.g. coated granules, impregnated granules and homogeneous granules, can be prepared by binding the active ingredients to solid carriers. The formulations of the invention comprise a herbicidally effective amount of the com- position of the present invention. The concentrations of the active the active ingredients in the formulations can be varied within wide ranges. In general, the formulations com- prise from 1 to 98% by weight, preferably 10 to 60 % by weight, of active ingredients (sum of pyroxasulfone, herbicide B and optionally further acitves). The active ingredi- ents are employed in a purity of from 90% to 100%, preferably 95% to 100% (according to NMR spectrum). The active compounds A and B and optionally further actives as well as the composi- tions 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 active compound (or composition) 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 active compound (or composition) 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. C Emulsifiable concentrates 15 parts by weight of active compound (or composition) are dissolved in 75 parts by weight of an organic solvent (eg. 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 active compound (or composition) are dissolved in 35 parts by weight of an organic solvent (eg. aikylaromatics) 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 active compound (or composition) 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 active compound (or composition) 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 active compound (or composition) 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 fonnnulations In a ball mill, 20 parts by weight of active compound (or composition), 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 I Dusts 5 parts by weight of active compound (or composition) 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. J Granules (GR, FG, GG, MG) 0.5 parts by weight of active compound (or composition) 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 U LV solutions (UL) 10 parts by weight of active compound (or composition) 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, wettable 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 compositions according to the invention of herbicides A and B and, if appropriate, safener on the growth of undesirable plants compared to the her- bicidally active compounds alone was demonstrated by the following greenhouse ex- periments: For the pre-emergence treatment, directly after sowing the active compounds, which had been suspended or emulsified in water, were applied by means of finely distributed nozzles. The containers were irrigated gently to promote germination and growth and subsequently covered with transparent plastic hoods until plant had rooted. This cover caused uniform germination of the tests plants, unless this was adversely affected by active compounds. For the post-emergence treatment, the test plants were first grown to a height of 3 to 20 cm, depending on the plant habit, and only then treated. Here, the herbicidal com- positions were suspended or emulsified in water as distribution medium and sprayed using finely distributing nozzles. The respective herbicides A and/or safener were formulated as 10% by weight strength emulsion concentrate and introduced to the spray liquor with the amount of solvent system used for applying the active compound. In the examples, the solvent used was water. Herbicide B and/or safener were used as commercially available formulations and introduced to the spray liquor with the amount of solvent system used for applying the active compound. In the examples, the solvent used was water. Metazachlor was used as a commercial aqueous suspension concentrate having an active ingredient concentration of 500 g/l. The test period extended over 21 days. During this time, the plants were tended, and their response to the treatments with active compound was evaluated. 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. The plants used in the greenhouse experiments belonged to the following species: Colby's formula was applied to determine whether the composition showed synergistic action. The value E, which is to be expected if the activity of the individual compounds is just additive, was calculated using the method of S. R. Colby (1967) "Calculating synergistic and antagonistic responses of herbicide combinations", Weeds 15, p. 22 ff. where X = effect in percent using herbicide A at an application rate a; Y = effect in percent using herbicide B at an application rate b; E = expected effect (in %) of A + B at application rates a + b. If the value observed in this manner is higher than the value E calculated according to Colby, a synergistic effect is present. An accelerated activity is observed when the damage 8 days after treatment (8 DAT) achieved by the combination shows a synergistic effect. Table 1a relates to the herbicidal activity of the individual actives in pre-emergence application assessed 8 DAT and 20 DAT. Table 1b relates the herbicidal activity of the combined actives in pre-emergence application assessed 8 DAT and 20 DAT. Table 2a relates to the herbicidal activity of the individual actives in post-emergence application assessed 8 DAT and 20 DAT. Table 2b relates the herbicidal activity of the combined actives in post-emergence application assessed 8 DAT and 20 DAT. Table 3 relates to the herbicidal activity of the individual actives and of the combina- tions in post-emergence application assessed 20 DAT. We claim: 1. A herbicidal composition comprising: a) a herbicide A which is 3-[5-(difiuoromethoxy)-1-methyl-3- (trifluoromethyl)pyrazol-4-ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2- oxazole; and b) at least one herbicide compound B which is an selected from VLCFA syn- thesis inhibitors. 2. The composition as claimed in claim 1, wherein the herbicide B is selected from the group consisting of b.1 chloroacetamide herbicides; and b.2 oxyacetamide herbicides. 3. The composition as claimed in claim 2, wherein the herbicide B comprises at least one chloroacetamide herbicide selected from the group consisting of ace- tochlor, dimethachlor, dimethenamid, dimethenamid-P, metazachlor, propi- sochlor, pethoxamide, metolachlor and metolachlor-S. 4. The composition as claimed in claim 3, wherein the herbicide B comprises di- methenamid or dimethenamid-P. 5. The composition as claimed in claim 4, wherein the herbicide B further comprises metazachlor. 6. The composition as claimed in claim 3, wherein the herbicide B comprises ace- tochlor. 7. The composition as claimed in claim 3, wherein the herbicide B comprises di- methachlor. 8. The composition as claimed in claim 3, wherein the herbicide B comprises propi- sochlor. 9. The composition as claimed in claim 3, wherein the herbicide B comprises meta- zachlor. 10. The composition as claimed in any of the preceding claims, further comprising a herbicide compound selected from quinmerac, aminopyralid, their salts and clo- mazone. 11. The composition as claimed in any of the preceding claims, further comprising a herbicide D which is selected from imidazolinone herbicides. 12. The composition as claimed in claim 11, wherein the imidazolinone herbicide is selected from the group consisting of imazamox, imazapic and their salts and their esters. 13. The composition as claimed in claim 12, wherein the herbicide B is metazachlor further comprising imazamox, a salt or ester thereof or a mixture of imazamox thereof and quinmerac, including mixtures of their salts and their esters. 14. The composition as claimed in claim 12, wherein the herbicide B is dimethenamid or dimethenamid-P further comprising imazapic or a salt thereof. 15. The composition as claimed in any of claims 1 to 11, additionally comprising a herbicide D, which is an inhibitor of the photosystem II. 16. The composition as claimed in claim 15, wherein the herbicide B is dimethenamid or dimethenamid-P. 17. The composition as claimed in any of claims 15 or 16, wherein the herbicide D is selected from the group consisting of d.1 arylurea herbicides; d.2 triazin(di)one herbicides; d.3 methylthiotriazine herbicides; and d.4 chlorotriazine herbicides. 18. The compositions as claimed in claim 15, wherein the herbicide D is selected from the group consisting of atrazin, terbuthylazine, diuron, metribuzin, ametryne, hexazinone and tebuthiuron. 19. The composition as claimed in claim 4, further comprising nicosulfuron. 20. The composition as claimed in any of claims 1 to 11, additionally comprising a herbicide D, which is an inhibitor of hydroxyphenylpyruvate dioxygenase. 21. The composition as claimed in claim 20, wherein the herbicide B is dimethenamid or dimethenamid P and wherein the herbicide D is topramezone. 22. The composition as claimed in claim 2, wherein the herbicide B comprises at least one oxyacetamide herbicide. 23. The composition as claimed in claim 22, wherein the herbicide B comprises flufenacet. 24. The composition as claimed in any of the preceding claims, containing no safener. 25. The composition as claimed in any of the preceding claims, wherein the relative amount of herbicide A to the at least one herbicide B is from 250:1 to 1:250. 26. The composition of claim 26, wherein the relative amount of herbicide A to the at least one herbicide B is from 100:1 to 1:100 provided the at least one herbicide B is an oxyacetamide herbicide. 27. The use of the compositions as claimed in any of the preceding claims for con- trolling undesirable vegetation. 28. The use as claimed In claim 27 for controlling undesirable vegetation in crop plants. 29. The use as claimed in claim 28, wherein the crops are crops of wheat, barley, rye, triticale, durum, rice, corn, sorghum, soybean, pulse crops, peanut, sugar cane, sunflower, cotton, potato, sugarbeet, brassica crops, turf, grapes, citrus, pistachio, stonefruits, pomefruits, garden ornamentals, bulb omamentals, coni- fers, deciduous trees, onion and garlic. 30. The use of a composition as claimed in any of claims 1 to 26 for controlling unde- sirable vegetation in crop plants, where the crop plants are resistant to herbicides acting as inhibitors of the VLCFA synthesis in plants. 31. A method for controlling undesirable vegetation, which comprises allowing a composition as claimed in any of claims 1 to 26 to act on plants to be controlled or their habitat. 32. A method for controlling undesired vegetation, which comprises applying a com- position as claimed in claims 1 to 26 before, during and/or after the emergence of the undesirable plants; the herbicides A and B being applied simultaneously or in succession. 33. An herbicide formulation comprising a composition as claimed in any of claims 1 to 26 and at least one solid or liquid carrier. The present invention relates to herbicidally active compositions, which comprise 3-[5-(difluoromethoxy)-1- methyl-3-(trifluoromethyl)pyrazol-4-ylmethylsulfonyl]-4,5-dihydro-5,5-dimethyl-1,2-oxazole [common name pyroxasulfone] and at least one herbicide B and at least one herbicide compound B which is an selected from inhibitors of the very long chain fatty acids (VLCFA) synthesis. The invention furthermore relates to the use of a composition as defined herein for controlling undesirable vegetation, in particular in crops. When using the compositions of the invention for this purpose the herbicide A and the at least one herbicide B can be applied simultaneously or in succession, where undesirable vegetation may occur. |
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| Patent Number | 279450 | |||||||||||||||
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| Indian Patent Application Number | 2952/KOLNP/2010 | |||||||||||||||
| PG Journal Number | 04/2017 | |||||||||||||||
| Publication Date | 27-Jan-2017 | |||||||||||||||
| Grant Date | 23-Jan-2017 | |||||||||||||||
| Date of Filing | 11-Aug-2010 | |||||||||||||||
| Name of Patentee | BASF SE | |||||||||||||||
| Applicant Address | 67056 LUDWIGSHAFEN GERMANY | |||||||||||||||
Inventors:
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| PCT International Classification Number | A01N 43/80 | |||||||||||||||
| PCT International Application Number | PCT/EP2009/052784 | |||||||||||||||
| PCT International Filing date | 2009-03-10 | |||||||||||||||
PCT Conventions:
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