Herbicidal compositions

The combination of herbicides (A) and (B) in a synergistic composition addresses the challenge of high application rates in existing herbicides, achieving effective weed control with reduced environmental impact and minimizing resistance development.

WO2025108865A1PCT designated stage expired Publication Date: 2025-05-30BAYER AG
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Patent Information

Application Number
PCT/EP2024/082650
Authority / Receiving Office
WO · WO
Patent Type
Applications
Current Assignee / Owner
Priority Date
2023-11-23
Filing Date
2024-11-18
Publication Date
2025-05-30

AI Technical Summary

Technical Problem

Existing herbicides often require high application rates to maintain effectiveness, which can lead to reduced selectivity and increased environmental impact, as well as potential resistance development in weeds.

Method used

A composition comprising herbicidally active compounds (A) and (B), where (A) is a compound of the general formula (I) or its agrochemically acceptable salts, and (B) is selected from a group of herbicides, which together provide a synergistic effect, reducing the required application rate while maintaining or enhancing herbicidal efficacy.

Benefits of technology

The combination of herbicides (A) and (B) achieves a synergistic effect, allowing for a reduction in application rates, improved weed control across a broader spectrum, and extended application periods, while minimizing environmental impact and resistance development.

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Abstract

The present invention relates to compositions comprising herbicidally active compounds (A) and (B), wherein (A) represents one or more compounds of the general formula (I) or agrochemically compatible salts thereof [component (A)], and (B) represents one or more herbicides [component (B)]. The application further relates to a process and to the use of the herbicidal composition of the invention for the control of harmful plants or for growth regulation.
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Description

[0001]BCS231024-Ausland STR 1 Bayer AG Herbicidal Compositions Description The invention lies in the technical field of plant protection agents which can be used against undesired plant growth in non-cultivated land, for seed pre-sowing protection or in plant crops and which contain a combination of at least two herbicides as herbicidal active ingredients, the compositions containing herbicidally active compounds (A) and (B), in which (A) denotes one or more compounds of the general formula (I) or their agrochemically acceptable salts [herbicides (A) or component (A)] and (B) denotes one or more herbicides (component B). Compounds from the structural class of the substituted N-phenyluracils are known as herbicides (see international application with the application number PCT / EP2023 / 077211).The compounds are effective against a broad spectrum of weeds both pre-emergence and post-emergence, allowing non-selective use to control unwanted plant growth or selective herbicide use in crops. The effectiveness of these herbicides against weeds is high, but generally depends on the application rate, the respective cultivation method, the weed spectrum, the weeds to be controlled, the climate and soil conditions, etc. Another criterion is the duration of action or the degradation rate of the herbicide. Changes in the potency of weeds, which may occur with prolonged use of the herbicides or due to geographical limitations, must also be taken into account. Losses in effectiveness in individual plants can only be compensated to a limited extent by high application rates of the herbicides, e.g.because this often impairs the selectivity of the herbicide or an improvement in effectiveness does not occur even with higher application rates. There is generally a need for methods to achieve herbicidal effectiveness with lower application rates of dry substances. A lower application rate not only reduces the amount of an active ingredient required for application, but generally also reduces the amount of suitable formulation aids. Both reduce the economic outlay and improve the biological tolerability of the herbicide treatment. One possibility for improving the application effectiveness of a herbicide can be to combine the active ingredient with one or more other substances that contribute the desired additional properties. However, the combined use of several active ingredients often leads to phenomena of physical and biological incompatibility, e.g.Lack of stability in a coformulation, interaction of an active ingredient, or antagonism of the active ingredients. What is desired, however, are combinations of active ingredients with a favorable action profile, high stability, and, if possible, an unexpectedly synergistically enhanced effect, which allows a reduction in the application rate compared to the individual application of the active ingredients to be combined. The object of the present invention was to provide alternative or advantageous herbicidal compositions which have a good biological application profile and, if possible, several of the above-mentioned desired favorable effects.Surprisingly, it has now been found that this object can be achieved by using a composition comprising herbicidally active compounds (A) and (B), where (A) denotes one or more compounds of the general formula (I) or their agrochemically acceptable salts [component (A)] and (B) denotes one or more herbicides [component (B)] selected from the group of herbicidally active compounds (B1) bBi1s1 (). The compositions according to the invention act in a particularly favorable manner, for example when they are used to combat undesirable plant growth in cultivated plants such as wheat (durum and soft wheat), maize, soybean, sugar beet, sugar cane, cotton, rice, beans (such as, for example, bush beans and horse beans), flax, barley, oats, rye, rice, potatoes and millet (sorghum), non-cultivated land, pastureland and green / lawn areas and plantation areas.The present invention relates to compositions comprising herbicidally active compounds (A) and (B), where (A) stands for one or more compounds of the general formula (I) or their agrochemically acceptable salts [component (A)]. where BCS231024-Foreign STR 3 R 1für Wasserstoff, Fluor, Chlor, Brom, Iod, Cyan Moe,thyl, Ethyl, Prop-1-yl, 1- Methylethyl, But-1-yl, 1-Methylpropyl, 2-Methylproypl, 1,1-Dimethylethyl, n-Pentyl, 1- Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1,1-Dimtheylpropyl, 1,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1-Ethylpropyl, n-Hexyl, 1-Methlpyentyl, 2-Methylpentyl, 3- Methylpentyl, 4-Methylpentyl, 1,1-Dimethylbutyl,21-,Dimethylbutyl, 1,3-Di- methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbuty 3l,,3-Dimethylbutyl, 1-Ethylbutyl, 2- Ethylbutyl, 1,1,2-Trimethylpropyl, 1,2,2-Trimethyrloppyl, 1-Ethyl-1-methylpropyl, 1- Ethyl-2-methylpropyl, Trifluormethyl, Difluormethy,l Pentafluorethyl, 2,2-Difluorethyl, 2,2,2-Trifluorethyl, Methoxy, Ethoxy, Prop-1-ylox Py,rop-2-yloxy, But-1-yloxy, But-2- yloxy, 2-Methylprop-1-yloxy, 1,1-Dimethyleth-1-yloyx, Difluormethoxy, Trifluormethoxy, Pentafluorethoxy, 2,2-Difluorethyo,x 2,2,2-Trifluorethoxy steht, R 2represents hydrogen, fluorine, chlorine, bromine, methyl, trimethyl, methoxy, ethoxy, prop-1-yloxy, but-1-yloxy, R 3 represents hydrogen, fluorine, chlorine, bromine, methoxy, ethoxy, prop-1-yloxy, prop-2-yloxy, but-1-yloxy, but-2-yloxy, 2-methylprop-1-yloxy, 1-,1-dimethyleth-1-yloxy, R 4 represents fluorine, chlorine, bromine, cyano, N2O, C(O)NH2, C(S)NH2, trifluoromethyl, difluoromethyl, pentafluoroethyl, ethynyl, propyn-1l, -y 1-butyn-1-yl, pentyn-1-yl, hexyn-1-yl, R 5 , R 6 and R 7unabhängig voneinander für Wasserstoff, Fluor,o Cr,h Blrom, Iod, Cyano, Methyl, Ethyl, Prop-1-yl, 1-Methylethyl, But-1-y 1l,-Methylpropyl, 2-Methylpropyl, 1,1-Dimethylethyl, n-Pentyl, 1-Methylbutyl, 2-Metlhbyutyl, 3-Methylbutyl, 1,1- Dimethylpropyl, 1,2-Dimethylpropyl, 2,2-Dimethylpproyl, 1-Ethylpropyl, n-Hexyl, 1- Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Mheytlpentyl, 1,1-Dimethylbutyl, 1,2-Dimethylbutyl, 1,3-Di-methylbutyl, 2,2-Dimethbyultyl, 2,3-Dimethylbutyl, 3,3- Dimethylbutyl, 1-Ethylbutyl, 2-Ethylbutyl, 1,1,2-Timrethylpropyl, 1,2,2- Trimethylpropyl, 1-Ethyl-1-methylpropyl, 1-Ethyl-m2-ethylpropyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, 2,2-Difluorethyl,22,2-Trifluorethyl, Methoxy, Ethoxy, Prop-1-yloxy, Prop-2-yloxy, But-1-yloxy, But-2-yloyx, 2-Methylprop-1-yloxy, 1,1- Dimethyleth-1-yloxy, Difluormethoxy, Trifluormethoyx, Pentafluorethoxy, 2,2-Difluorethoxy, 2,2,2-Trifluorethoxy stehen, G für Methylen, (Methyl)methylen, (Ethyl)methyle (nP,rop-1-yl)methylen,(Prop-2- yl)methylen, (But-1-yl)methylen, (But-2-yl)methyl,e (nPent-1-yl)methylen, (Pent-2- BCS231024-Ausland STR 4 yl)methylen, (Pent-3-yl)methylen, (Dimethyl)methny,le (Diethyl)methylen, Ethylen, n- Propylen, (1-Methyl)ethyl-1-en, (2-Methyl)ethyl-1n-,e n-Butylen, 1-Methylpropyl-1-en, 2-Methylpropyl-1-en, 3-Methylpropyl-1-en, 1,1-Dimheytlethyl-1-en, 2,2-Dimethylethyl- 1-en, 1-Ethylethyl-1-en, 2-Ethylethyl-1-en, 1-(P-r1o-pyl)ethyl-1-en, 2-(Prop-1-yl)ethyl- 1-en, 1-(Prop-2-yl)ethyl-1-en, 2-(Prop-2-yl)ethy-le-1n, 1,1,2-Trimethylethyl-1-en, 1,2,2- Trimethylethyl-1-en, 1,1,2,2-Tetramethylethyl-1-e nn-P,entylen, 1-Methylbutyl-1-en, 2- Methylbutyl-1-en, 3-Methylbutyl-1-en, 4-Methylbu-ty1l-en, 1,1-Dimethylpropyl-1-en, 2,2-Dimethylpropyl-1-en, 3,3-Dimethylpropyl-1-en,,21-Dimethylpropyl-1-en, 1,3- Dimethylpropyl-1-en, 1-Ethylpropyl-1-en, n-Hexyle 1n-,Methylpentyl-1-en, 2- Methylpentyl-1-en, 3-Methylpentyl-1-en, 4-Methylptyeln-1-en, 1,1-Dimethylbutyl-1-en, 1,2-Dimethylbutyl-1-en, 1,3-Dimethylbutyl-1-ene, 2,3-Dimethylbutyl-1-ene, 3,3-Dimethylbutyl-1-ene, 1-Ethylbutyl-1-ene, 2-Ethylbutyl-1-ene, 1,1,2-Trimethylpropyl-1-ene, 1,2,2-Trimethylpropyl-1-ene, 1-Ethyl-1-methylpropyl-1-ene, 1-Ethyl-2-methylpropyl-1-ene, X and Y independently represent O (oxygen sulfide) or S (sulfur) and Q represents one of the groups Q-1 to Q-25 specifically mentioned below, where in the structural formulas of the table below, the formula represents a bond of the respective group Q to the carbonyl group in the general formula (eI)h: Q-1 Q-2 Q-3 Q-4 Q-5 Q-6 Q-7 Q-8 Q-9 Q-10 BCS231024-Ausland STR 5 Q-11 Q-12 Q-13 Q-14 Q-15 Q-16 Q-17 Q-18 Q-19 Q-20 Q-21 Q-22 Q-23 Q-24 Q-25 and (B) represents one or more herbicides [component (aBu)]s from the group of herbicidal active ingredients (B1) to (B11), wherein (B1) represents herbicidal active ingredients from the group of the 1,3-diketo compounds mentioned below (B1.1) Alloxydim, (CAS 55634-91-8),(CAS 55635-13-7) (B1.2) Bicyclopyrone, (CAS 352010-68-5) (B1.3) Butroxydim, (CAS 138164-12-2) (B1.4) Clethodim, (CAS 99129-21-2) (B1.2) Clethodim (CAS 99129-21-21) C.C.C. 101205-02-1) (B1.6) Fenquinotrione, (CAS 1342891-70-6) (B1.7) Mesotrione, (CAS 104206-82-8) (B1.8) Pinoxaden, (CAS 243973-20-8) (CAS1.9) (CAS1.9) 139001-49-3) (B1.10) Sethoxydim, (CAS 74051-80-2) (B1.11) Sulcotrione, (CAS 99105-77-8) (B1.12) SYP-9121 (CAS 1976053-87-87-8) STRCS-Ausland 2426 (B1.13) Tefuryltrione, (CAS 473278-76-1) (B1.14) Tembotrione, (CAS 335104-84-2) (B1.15) Tepraloxidim, (CAS 149979-41-9) (B1.16) Tralkoxydim, (CAS 473278-80-88) (B1.17) Y13161, (CAS 1639426-14-4) (B1.18) Y13287 (CAS 1639426-42-8) (B2) for herbizide Werkstoffe aus der Gruppe decrh nfaolgend genannten (Sulhfont, Acetochlor, 211) Acetoch. (CAS 34256-82-1) (B2.2) Alachlor, (CAS 15972-60-8) (B2.3) Amidosulfuron, (CAS 120923-37-7) (B2.4) Asulam, (CAS 3337-71-1), (CAS 140-8), (CAS-43-13) 2302-17-2) (B2.5) Azimsulfuron,(CAS 120162-55-2) (B2.6) Beflubutamid, (CAS 113614-08-7), (CAS 113614-09-8) (B2.7) Bensulfuron, (CAS 83055-99-6), (CAS 83055-99-6) (B2.8) Butachlor, (CAS 23184-66-99) (B2.9) Carbetamide, (CAS 16118-49-3) (B2.10) Chlorimuron, (CAS 99283-00-8), (CAS 90982-32-4) (B2.11) Chlorpropham, (CAS 101-21-3) (B2.12) Chlorsulfuron, (CAS 64902-72-3) (B2.13) Cinosulfuron, (CAS 94593-91-6) (B2.14) Cloransulam, (CAS159518-97-5), (CAS 147150-35-4) (B2.15) Cyclosulfamuron, (CAS 136849-15-5) (B2.16) Desmedipham, (CAS 13684-56-5) (B2.17) Diclosulam, (CAS 145701-21-9) (B2.18) Diflufenican, (CAS 83164-33-4) (B2.19) Dimethachlor, (CAS 50563-36-5) (B2.20) Dimethenamid, (CAS 87674-68-8), (CAS 163515-14-8) (B2.21) Esprocarb (CAS 85785-20-2) BCS231024-Ausland STR 7 (B2.22) Ethametsulfuron, (CAS 111353-84-5), (CAS 97780-06-8) (B2.23) Ethoxysulfuron, (CAS 126801-58-9) (B2.24) Flazasulfuron, (CAS 104040-78-0) (B2.25) Florasulam, (CAS 145701-23-1) (B2.26) Flucarbazone, (CAS 145026-88-6),(CAS 181274-17-9) (B2.27) Flucetosulfuron, (CAS 412928-75-7) (B2.28) Flufenacet, (CAS 142459-58-3) (B2.29) Flumetsulam, (CAS 98967-40-9) (B2.30) Flupyrsulfuron, (CAS 150315-10-9), (CAS 144740-53-4), (CAS 144740-54-5) (B2.31) Foramsulfuron, (CAS 173159-57-4) (B2.32) Halosulfuron, (CAS 135397-30-7), (CAS 100784-20-1) (B2.33) Imazosulfuron, (CAS 122548-33-8) (B2.34) Iodosulfuron, (CAS 185119-76-0), (CAS 144550-06-1), (CAS 144550-36-7) (B2.35) Ipfencarbazone, (CAS 212201-70-2) (B2.36) Mefenacet, (CAS 73250-68-7) (B2.37) Mesosulfuron, (CAS 400852-66-6), (CAS 208465-21-8) (B2.38) Metazachlor, (CAS 67129-08-2) (B2.39) Metazosulfuron, (CAS 868680-84-6) (B2.40) Metolachlor, (CAS 51218-45-2) (B2.41) Metosulam, (CAS 139528-85-1) (B2.42) Metsulfuron, (CAS 79510-48-8), (CAS 74223-64-6) (B2.43) Nicosulfuron, (CAS 111991-09-4) (B2.44) Orthosulfamuron, (CAS 213464-77-8) (B2.45) Oxasulfuron, (CAS 144651-06-9) (B2.46) Penoxsulam, (CAS 219714-96-2) (B2.47) Pethoxamide,(CAS 106700-29-2) (B2.48) Phenmedipham, (CAS 13684-63-4) BCS231024-Ausland STR 8 (B2.49) Picolinafen, (CAS 137641-05-5) (B2.50) Pretilachlor, (CAS 51218-49-6) (B2.51) Primisulfuron, (CAS 113036-87-6), (CAS 86209-51-0) (B2.52) Propachlor, (CAS 1918-16-7) (B2.53) Propanil, (CAS 709-98-8) (B2.54) Propham, (CAS 122-42-9) (B2.55) Propisochlor, (CAS 86763-47-5) (B2.56) Propoxycarbazone, (CAS 145026-81-9), (CAS 181274-15-7) (B2.57) Propyrisulfuron, (CAS 570415-88-2) (B2.58) Propyzamide, (CAS 23950-58-5) (B2.59) Prosulfocarb, (CAS 52888-80-9) (B2.60) Prosulfuron, (CAS 94125-34-5) (B2.61) Pyrazosulfuron, (CAS 98389-04-9), (CAS 93697-74-6) (B2.62) Pyroxsulam, (CAS 422556-08-9) (B2.63) Rimsulfuron, (CAS 122931-48-0) (B2.64) S-metolachlor, (CAS 87392-12-9) (B2.65) Sulfometuron, (CAS 74223-56-6), (CAS 74222-97-2), (CAS 144651-06-9) (B2.66) Sulfosulfuron, (CAS 141776-32-1) (B2.67) Thenylchlor, (CAS 96491-05-3) (B2.68) Thiencarbazone, (CAS 936331-72-5), (CAS 317815-83-1) (B2.69) Thifensulfuron,(CAS 79277-67-1), (CAS 79277-27-3) (B2.70) Tri-allat, (CAS 2303-17-5) (B2.71) Triasulfuron, (CAS 82097-50-5) (B2.72) Tribenuron, (CAS 106040-48-6), (CAS 101200-48-0) (B2.73) Trifloxysulfuron, (CAS 145099-21-4, (CAS 199119-58-9) (B2.74) Triflusulfuron, (CAS 135990-29-3), (CAS 126535-15-7) BCS231024-Ausland STR 9 (B2.75) Tritosulfuron, (CAS 142469-14-5) (B2.76) Esprocarb, (CAS 85785-20-2) (B2.77) Profluazol, (CAS 190314-43-3) (B2.78) Tri-allate, (CAS 2303-17-5) (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5- methoxy-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5- vinyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.81) Icafolin-methyl (CAS 2749998-21-6; CAS 2254752-27-5)), (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l- methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)- vinyl-4H-isoxazol-5-carbonyl]amino]-2,3- dihydrofuran-5-carboxylat, (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)- methyl-4H-isoxazol-5-carbonyl]amino]-2,3- dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5- vinyl-4H-1,2-oxazol-5-yl]carbonyl]amino]- cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-5- methoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o- fluorphenyl)-5-(trifluormethyl)-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl- 4H-1,2-oxazol-5-yl]carbonyl]amino]cyclopenten-1- carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-l5)- methyl-4H-1,2-oxazol-5-yl]carbonyl]amino]- cyclopenten-1-carboxylat, BCS231024-Ausland STR 10 (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2- ylcarbonyl)cyclopent-2-en-1-yl]-5-(trifluormethyl)- 4H-1,2-oxazol-5-carboxamid, (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-[(propylsulfonylamino)carbonyl]cyclopent-2-en-1-yl]-5-(trifluoromethyl)-4H-1,2-oxazole-5-carboxamide, (B2.92) (1S,4R)-4-[[(5R)-3-(3,5-difluorophenyl)-5e-methyl- 4H-isoxazole-5-carbonyl]amino]cyclopent-2-ene-1-carboxylic acid (B2.93) 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-[-(3S)-methylsulfinyl]-4-(trifluoromethyl)benzamide (CAS 2833716-54-2) (B3) represents herbicidal active ingredients from the group of the arylnitriles mentioned below (B3.1) Bromoxynil, (CAS 1689-84-5) (CAS 3861-41-4), (CAS 56634-95-8), (CAS 1689-99-2), (CAS 2961-68-4) (B3.2) Chlorothiamide, (CAS 1918-13-4) (B3.3) Dichlobenil, (CAS 1194-65-6) (B3.4) Ioxynil, (CAS 1689-83-4), (CAS 2961-61-7), (CAS 3861-47-0), (CAS 2961-62-8) (B3.5) Pyraclonil (CAS 158353-15-2) (B4) represents herbicidal active ingredients from the group of the azoles mentioned below (B4.1) Amicarbazone, (CAS 129909-90-6) (B4.2) Amitrole, (CAS 61-82-5) (B4.3) Azafenidine, (CAS 68049-83-2) (B4.4) Benzofenap,(CAS 82692-44-2) (B4.5) Benzuofucaotong (CAS 1992017-55-6) (B4.6) Biscarfentrazone (CAS 1622908-18-2) (B4.7) Cafenstrole, (CAS 125306-83-4) (B4.8) Carfentrazone, (CAS 128621-72-7), (CAS128-0623-91) (B4.9) Fentrazamide, (CAS 158237-07-1) (B4.10) Imazamethabenz, (CAS 100728-84-5), (CAS0851-845-8) (B4.11) Imazamox, (CAS 114311-32-9), (CAS 247057-3-2)2 (B4.12) Imazapic, (CAS 104098-48-8), (CAS 115136-3-5)3 BCS231024-Ausland STR 11 (B4.13) Imazapyr, (CAS 81334-34-1), (CAS 81510-8)3-0 (B4.14) Imazaquin, (CAS 81335-37-7), (CAS 813359-4),7- (CAS 81335-43-5), (CAS 81335-46-8) (B4.15) Imazethapyr, (CAS 81335-77-5), (CAS 10196167-2-) (B4.16) Isouron, (CAS 55861-78-4) (B4.17) Isoxaben, (CAS 82558-50-7) (B4.18) Isoxaflutole, (CAS 141112-29-0) (B4.19) Oxadiargyl, (CAS 39807-15-3) (B4.20) Oxadiazon, (CAS 19666-30-9) (B4.21) Pyraflufen, (CAS 129630-17-7), (CAS 12961390--9) (B4.22) Pyrasulfotole, (CAS 365400-11-9) (B4.23) Pyrazolynate, (CAS 58011-68-0) (B4.24) Pyrazoxyfen,(CAS 71561-11-0) (B4.25) Pyroxasulfone, (CAS 447399-55-5) (B4.26) Sulfentrazone, (CAS 122836-35-5) (B4.27) Tolpyralate, (CAS 1101132-67-5) (B4.28) Toprazone, (CAS 210631-68-8) (B4.29) Triazolesulcotrione (CAS 1911613-97-2) (QYR-301), (B4.30) QYM-201, (CAS 1855925-45-1) (B4.31) Bencarbazone, (CAS 173980-17-1) (B4.32) Fluazolate, (CAS 174514-07-9) (B4.33) Flupoxam, (CAS 119126-15-7) (B4.34) Isoxachlortole (CAS 141112-06-3) (B5) Further subsequently named herbicide Wstiorffe steht, (B5.1) Aminocyclopyrachlore, (CAS 858956-08-8), (CAS 8S58954-83-3), (CAS 858956-35-1) (B5.2) Aminopyralid, (CAS 150114-71-9), (CAS 5661-8971-5), (CAS 566191-89-7) (B5.3) Benazoline-ethyl, (CAS 3813-05-6), (CAS 38-57661-1), (CAS 25059-80-7), (CAS 67338-65-2) (B5.4) Benfluralin, (CAS 1861-40-1) (B5.5); Bentazone, (CAS 25057-89-0), (CAS 50723-)80-3 (B5.6) Benzobicyclone, (CAS 156963-66-5) (B5.7) Bixlozone (CAS 81777-95-9) BCS231024-Ausland STR 12 (B5.8); Bromophenoxime, (CAS 13181-17-4) (B5.9) Butralin,(CAS 33629-47-9) (B5.10) Chloridazon / Pyrazon, (CAS 1698-60-8) (B5.11) Chlorthal, (CAS 2136-79-0), (CAS 1861-32,-1) (CAS 887-54-7) (B5.12) Cinidon-ethyl, (CAS 142891-20-1) (B5.13) Cinmethylin, (CAS 87818-31-3) (B5.14) Clomazone, (CAS 81777-89-1) (B5.15) Cyclopyrimorat, (CAS 499231-24-2) (B5.16) Dinitramine, (CAS 29091-05-2) (B5.17) Diquat, (CAS 2764-72-9), (CAS 85-00-7), (CAS 4032-26-2) (B5.18) Dithiopyr, (CAS 97886-45-8) (B5.19) Essigsäure, (CAS 64-19-7) (B5.20) Ethalfluralin, (CAS 55283-68-6) (B5.21) Ethofumesate, (CAS 26225-79-6) (B5.22) Flamprop, (CAS 58667-63-3, (CAS 90134-5,9-1) (CAS 63782-90-1), (CAS 63729-98-6) (B5.23) Florpyrauxifen, (CAS 943832-81-3), (CAS 1036961-72-9) (B5.24) Flufenpyr, (CAS 188490-07-5), (CAS 1884879--80) (B5.25) Flumiclorac, (CAS 87547-04-4), (CAS 875486--71) (B5.26) Flumioxazin, (CAS 103361-09-7) (B5.27) Fluridone, (CAS 59756-60-4) (B5.28) Flurochloridone, (CAS 61213-25-0) (B5.29) Flurtamone, (CAS 96525-23-4) (B5.30) Fluthiacet-methyl,(CAS 149253-65-6) (B5.31) Halauxifen, (CAS 943832-60-8), (CAS 94389381--9) (B5.32) Indanofan, (CAS 13320-30-1) (B5.33) Norflurazon, (CAS 27314-13-2) (B5.34) Oleinsäure (CAS 112-80-1) (B5.35) Oryzalin, (CAS 19044-88-3) (B5.36) Oxaziclomefone, (CAS 153197-14-9) (B5.37) Paraquat, (CAS 4685-14-7), (CAS 1910-42-5), (CAS 2074-50-2) (B5.38) Pelargonsäure, (CAS 112-05-0) (B5.39) Pendimethalin, (CAS 40487-42-1) BCS231024-Ausland STR 13 (B5.40) Pentoxazone, (CAS 110956-75-7) (B5.41) Pyridafol, (CAS 40020-01-7) (B5.42) Pyridate, (CAS 55512-33-9) (B5.43) Tetflupyrolimet, (CAS 2053901-33-8) (B5.44) Thiazopyr, (CAS 117718-60-2) (B5.45) Triafamon, (CAS 874195-61-6) (B5.46) Trifluralin, (CAS 1582-09-8) (B5.47) 4-Amino-3-chloro-5-fluoro- 6-(7-fluoro-1H-indol-6- yl)pyridine-2-carbonsäure (B5.48) Cyclopyrimorate, (CAS 499231-24-2) (B5.49) Diquat, (CAS 2764-72-9), (CAS 85-00-7), (CAS4032-26-2) (B5.50) Oxaziclomefone, (CAS 153197-14-9) (B5.51) Pentanochlor, (CAS 2307-68-8) (B5.52) Tebutam,(CAS 35256-85-0) (B5.53) Thidiazimin, (CAS 123249-43-4) (B5.54) 4-Hydroxy-1-methyl-3-[4- (CAS 1708087-22-2) (trifluoromethyl)-2- pyridinyl]-2-imidazolidinon (B5.55) MSMA, (CAS 2163-80-6)(B6) herbicidal active ingredients from the group of the (het)arylcarboxylic acids mentioned below are (B6.1) Chloramben, (CAS 133-90-4), (CAS 1076-46-6), (CAS 53404-16-3), (CAS 7286-84-2), (CAS 25182-03-0), (1954-81-0) (B6.2) Clopyralid, (CAS 1702-17-6 ()C, AS 1532-24-7), (CAS 57754-85-5), (CAS 58509-83-4), (CAS 73455-09-1) (B6.3) Dicamba, (CAS 1918-00-9 ()C, AS 1286239-22-2), (CAS 104040-79-1), (CAS 2300-66-5), (CAS 25059-78-3), (CAS 55871-02-8), (CAS 6597-78-0), (CAS 53404-28-7), (CAS 10007-85-9), (CAS 1982-69-0), (53404-29-8), (CAS 56141-00-5) BCS231024-Ausland STR 14 (B6.4) Fluroxypyr, (CAS 69377-81-7), (CAS -27-8), (CAS 81406-37-3) (B6.5) Picloram, (CAS 1918-02-1), (CAS 55870-98-9), (CAS 36374-99-9), (CAS 26952-20-5), (CAS 14143-55-6), (CAS 55871-00-6), (CAS 2545-60-0), (CAS 35832-11-2), (CAS 6753-47-5), (CAS 82683-78-1) (B6.6) Quinclorac, (CAS 84087-01-4), (CAS 84087-94)8,- (CAS 84087-33-2) (B6.7) Quinmerac, (CAS 90717-03-6) (B6.8) TBA, (CAS 50-31-7), (CAS 3426-62-8),(CAS 71750-37-3), (CAS 4559-30-2), (CAS 2078-42-4) (B6.9) Triclopyr (CAS 55335-06-3), (CAS 64700-56),-7 (CAS 1048373-85-8), (CAS 60825-27-6), (CAS 57213-69-1) (B7) represents herbicidal active ingredients from the group of organic phosphorus compounds mentioned below: (B7.1) Anilofos, (CAS 64249-01-0) (B7.2) Bialaphos, (CAS 35597-43-4), (CAS 71048-9)9-2 (B7.3) Butamifos, (CAS 36335-67-8) (B7.4) Glufosinate, (CAS 51276-47-2), (CAS 35597-5-4)4, (CAS 77182-82-2) (,CAS 70033-13-5) (B7.5) Glyphosate, (CAS 1071-83-6), (CAS 69254-4),0-6 (CAS 34494-04-7), (CAS 38641-94-0), (CAS 40465-66-5), (CAS 39600-42-5), (CAS 70393-85-0), (CAS 81591-81-3) (B7.6) Piperophos, (CAS 24151-93-7) (B7.7) Sulfosate, (CAS 1591-81-3) (B7.8) Amiprofos (CAS 33857-23-7, (CAS 36001-88-4) BCS231024-Ausland STR 15 (B8) for herbicidal active substances from the group of the phenyl ethers mentioned below (B8.1) 2,4-D, (CAS 94-75-7), (CAS 2307-55-3), (CAS 1929-73-3), (CAS 1320-18-9), (CAS 1928-45-6), (CAS 94-80-4),(CAS 1048373-72-3), (CAS 20940-37-8), (CAS 2008-39-1), (CAS 5742-19-8), (CAS 2212-54-6), (CAS 533-23-3), (CAS 1928-43-4), (CAS 37102-63-9), (CAS 713-15-1), (CAS 25168-26-7), (CAS 94-11-1), (CAS 5742-17-6), (CAS 3766-27-6), (CAS 1917-97-1), (CAS 1928-38-7), (CAS 1928-44-5), (CAS 1917-92-6), (CAS 1928-61-6), (CAS 2702-72-9), (CAS 15146-99-3), (CAS 28685-18-9), (CAS 2646-78-8), (CAS 18584-79-7), (CAS 2569-01-9), (CAS 215655-76-8) (B8.2) 2,4-DB, (CAS 94-82-6), (CAS 2758-42-1), (CAS 1320-15-6), (CAS 19480-40-1), (CAS 10433-59-7) (B8.3) 2,4-DP, (CAS 120-36-5), (CAS 53404-31-2), (CAS 53404-32-3), (CAS 79270-78-3), (CAS 28631-35-8), (CAS 57153-17-0), (CAS 5746-17-8), (CAS 39104-30-8) (B8.4) Acifluorfen, (CAS 50594-66-6), (CAS 50594-76)7, (CAS 62476-59-9) (B8.5) Aclonifen, (CAS 74070-46-5) (B8.6) Bifenox, (CAS 42576-02-3) (B8.7) Chlomethoxyfen, (CAS 32861-85-1) (B8.8) Clodinafop- (CAS 114420-56-3), (CAS 105512-06-9) propargyl, (B8.9) Clomeprop, (CAS 84496-56-0) (B8.10) Cyhalofop,(CAS 122008-78-0), (CAS 1220058-9-8) (B8.11) Diclofop, (CAS 40843-25-2), (CAS 51338-2)7-3 (B8.12) Ethoxyfen, (CAS 188634-90-4), (CAS 1310826-5-4) BCS231024-Ausland STR 16 (B8.13) Fenoxaprop, (CAS 95617-09-7), (CAS 113150-80-)4, (CAS 71283-80-2) (B8.14) Fluazifop, (CAS 69335-91-7), (CAS 83066-08)8,- (CAS 79241-46-6) (B8.15) Fluoroglycofen, (CAS 77501-60-1), (CAS 771-5900-7) (B8.16) Fomesafen, (CAS 72178-02-0), (CAS 10873-10-)70 (B8.17) Halosafen, (CAS 77227-69-1) (B8.18) Haloxyfop, (CAS 69806-34-4), (CAS 95977-02)9,- (CAS 72619-32-0) (B8.19) Lactofen, (CAS 77501-63-4) (B8.20) MCPA, (CAS 94-74-6), (CAS 19480-43-4), (CAS 1713-12-8), (CAS 2039-46-5), (CAS 20405-19-0), (CAS 2698-38-6), (CAS 29450-45-1), (CAS 1713-11-7), (CAS 26544-20-7), (CAS 2698-40-0), (CAS 2436-73-9), (CAS 6365-62-4), (CAS 5221-16-9), (CAS 3653-48-3), (CAS 42459-68-7) (B8.21) MCPB, (CAS 94-81-5), (CAS 10443-70-6), (CAS 57153-18-1), (CAS 6062-26-6) (B8.22) Mecoprop, (CAS 93-65-2), (CAS 32351-70-5), (CAS 1432-14-0),(CAS 71526-69-7), (CAS 28473-03-2), (CAS 2786-19-8), (CAS 1929-86-8), (CAS 19095-88-6), (CAS 53404-61-8), (CAS 16484-77-8) (B8.23) Metamifop, (CAS 256412-89-2) (B8.24) Oxyfluorfen, (CAS 42874-03-3) (B8.25) Propaquizafop, (CAS 111479-05-1) (B8.26) Quizalofop, (CAS 76578-12-6), (CAS 765748--81), (B8.27) Quizalofop-P, (CAS 94051-08-8), (CAS 100-65416-3), (CAS 200509-41-7) (B8.28) Benzfendizone (CAS 158755-95-4) BCS231024-Ausland STR 17 (B9) stands for herbicidal active ingredients from the group of the following pyrimidines / triazines (B9.1) Bispyrac-sodium, (CAS 125401-92-5) (B9.2) Bromacil, (CAS 314-40-9), (CAS 53404-19-6), (CAS 69484-12-4) (B9.3) Butafenacil, (CAS 134605-64-4) (B9.4) Lenacil, (CAS 2164-08-1) (B9.5) Pyribenzoxime, (CAS 168088-61-7) (B9.6) Pyriftalide, (CAS 135186-78-6) (B9.7) Pyriminobac, (CAS 136191-56-5), (CAS 136191-64-5) (B9.8) Pyrimisulfan, (CAS 221205-90-9) (B9.9) Pyrithiobac sodium, (CAS 123342-93-8), (C 1A2S3343-16-8) (B9.10) Saflufenacil,(CAS 372137-35-4) (B9.11) Terbacil, (CAS 5902-51-2) (B9.12) Tiafenacil, (CAS 1220411-29-9) (B9.13) Trifludimoxazine, (CAS 1258836-72-4) (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1- (CAS 353292-31-6)methyl-6-trifluoromethyl-2,4-dioxo- 1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3- (CAS 1949837-17-5) methyl-2,6-dioxo-4-(trifluoromethyl)- 3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro- 1,2-oxazole-5-carboxylate (B9.16) 3-[2-chloro-5-(3,5-dimethyl-2,6- (CAS 2558200-03-4) dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4- (CAS 2669111-31-1) fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)- yl]benzylidene}amino]oxy}propanoate BCS231024-Ausland STR 18 (B9.18) Flufenoximacil (CAS 2759011-88-4) (B10) for herbicidal active substances from the group of (thio)ureas mentioned below (B10.1) Chlorobromuron,(CAS 13360-45-7) (B10.2) Chlorotoluron, (CAS 15545-48-9) (B10.3) Daimuron, (CAS 42609-52-9) (B10.4) Dimefuron, (CAS 34205-21-5) (B10.5) Diuron, (CAS 330-54-1) (B10.6) Diflufenzopyr (CAS 1957168-02-3) (B10.7) Fluometuron, (CAS 2164-17-2) (B10.8) Isoproturon, (CAS 34123-59-6) (B10.9) Linuron, (CAS 330-55-2) (B10.10) Methabenzthiazuron, (CAS 18691-97-9) (B10.11) Metobromuron, (CAS 3060-89-7) (B10.12) Metoxuron, (CAS 19937-59-8) (B10.13) Monolinuron, (CAS 1746-81-2) (B10.14) Neburon, (CAS 555-37-3) (B10.15) Siduron, (CAS 1982-49-6) (B10.16) Tebuthiuron, (CAS 34014-18-1) (B10.17) Fenuron, (CAS 101-42-8) (B10.18) Chloroxuron, (CAS 1982-47-4) (B10.19) Diflufenzopyr, (CAS 1957168-02-3, CAS 109293-98-3) (B10.20) Ethidimuron (CAS 30043-49-3) (B11) herbicidal active substances from the group of the following triazines are: (B11.1) Ametryne, (CAS 834-12-8) (B11.2) Atrazine, (CAS 1912-24-9) (B11.3) Cyanazine, (CAS 21725-46-2) (B11.4) Dimethametryn, (CAS 22936-75-0) (B11.5) Hexazinone,(CAS 51235-04-2) (B11.6) Indaziflam, (CAS 950782-86-2) (B11.7) Metamitron, (CAS 41394-05-2) (B11.8) Metribuzin, (CAS 21087-64-9) (B11.9) Prometon, (CAS 1610-18-0) (B11.10) Prometryne, (CAS 7287-19-6) BCS231024-Ausland STR 19 (B11.11) Propazine, (CAS 139-40-2) (B11.12) Simazine, (CAS 122-34-9) (B11.13) Simetryne, (CAS 1014-70-6) (B11.14) Terbumetone, (CAS 33693-04-8) (B11.15) Terbuthylazine, (CAS 5915-41-3) (B11.16) Terbutryne, (CAS 886-50-0) (B11.17) Triaziflam, (CAS 131475-57-5) (B11.18) Trietazine, (CAS 1912-26-1) (B11.19) Desmetryne (CAS 1014-69-3). The names of the herbs listed above (e.g., Cidoemmon name) are supplemented by the "CAS RN" (Chemical Abstract Service Number) (abbreviated to "CAS") in parentheses. The CASRN is a commonly used reference number that allows for a clear assignment of the designated substances, since the "CASRN" distinguishes between their isomers, including stereoisomers, as well as salts and esters. For active substances,Since they exist in various forms, the name of the neutralizing agent is given in the list above. The CAS numbers given in brackets refer to these, as well as to all other recognized forms of the active ingredient, such as salts or adducts. Examples, but not limited to: 2,4-D-ammonium; 2,4-D-choline (the choline salt of 2o,n4-D); 2,4-D-BAPMA (N,N-bis-(3-aminopropyl)methylamine salt of 2,4-D); 2,4-D-dimethylammonium; 2,4-D-dodecylammonium; 2,4-D-heptylammonium; 2,4-D-isopropylammonium; 2,4-D-lithium; 2,4-D-potassium; 2,4-D-sodium; 2,4-D-tetradecylammonium; 2,4-D-triethylammonium; 2,4-D-tris(2-hydroxypropyl)ammonium; 2,4-D-monoethanolammonium (monoethanolamine salt of 2,4-D); 2,4-D-diethanolammonium (the diethanolamine salt of 2,4-D or 2,4-D-diolamine); 2,4-D-triethanolammonium (the triethanolamine salt of 2,4-D or 2,4-D-Triolamine); the tetrabutylamine salt of dicamba; the dimethylamine salt of dicamba; isopropylamine salt of dicamba; the diglycolamine salt of dicamba; the N,N-bis-(3-amphinyl)methylamine salt of dicamba; the choline salt of dicamba; the monoethanolamine salt of dicamba; the diethanolamine salt of dicamba; the triethanolamine salt of dicamba; diglyphosate Km salt of dicamba; the sodium salt of dicamba; glyphosate diammonium; glyphosate dimethyl ammonium; glyphosate isopropylammonium; glyphosate monoammonium; glyphosate potassium; glyphosate dipotassium; glyphosate sesquisodium (N-(phosphonomethyl)glycine sodium salt (2:3)); the tert-butylsulfonium salt of glyphosate (glyphosate-trimesium); the triethanolamine salt of glyphosate; the diethanolamine salt of glyphosate; and the monoethanolamine salt of glyphosate. BCS231024-Ausland STR 20 In the following, only the neutral compound is used, thus including all existing forms as listed, unlessA specific form of the active ingredient is relevant in a particular context, as in the following examples of biological activity. The compositions according to the invention may contain other components, e.g. other active ingredients against harmful organisms such as pests, animals, or fungi harmful to plants, in particular substances from the group of herbicides, fungicides, insecticides, acaricides, nematicides, and miticides and related substances, or also other types of plant protection active ingredients (e.g., fungicides), crop-protecting active ingredients (safeners, antidotes), plant growth inhibitors, and / or additives and / or formulation aids commonly used in plant protection. The components can be formulated and applied together (ready-made formulation) or can be formulated separately and applied together.e.g., in a tank mix or in sequential application. The individual herbicidal active ingredients of the general formula (I) contained as component (A) are also referred to below as compounds (A), active ingredient (A), components (A), or herbicides (A). Accordingly, the individual herbicidal active ingredients contained as component (B) are also referred to below as compounds (B), active ingredient (Bs), components (B), or herbicides (B). An advantageous property of the inventive combination of herbicides (A) and (B) is that active ingredients (A) and (B) are compatible with each other, i.e., they can be used together without significant chemical differences between the active ingredients (A) and / or (B).which lead to the decomposition of one or more of the active ingredients. This avoids a reduction in the active ingredient content in formulations or sprays. The favorable compatibility also extends to the biological properties of the active ingredients in combined use. Thus, antagonistic effects are generally not observed when controlling weeds with the active ingredient combinations according to the invention. The active ingredients (A) and (B) are therefore particularly suitable for use together or in addition to other crop protection agents or agrochemicals. The possible combined use allows the utilization of advantageous effects, such as the expansion of the spectrum of weeds to be controlled or combated in one application.The application rate of the individual herbicides (A) or (B) can be reduced compared to the respective application rate of the herbicide in question when applied individually. This can influence the degradation behavior of the active ingredients and create more favorable conditions for the subsequent cultivation of crops. A further advantage is that the development of resistance to the active ingredients can often be significantly reduced or prevented by combining active ingredients with different modes of action. In particular, surprisingly, superadditive (= synergistic) effects occur when the active ingredients (A) and (B) are applied separately on a larger number of economically important crops. The effect in the combination is stronger than the expected sum of the effects of the individual herbicides used. The synergistic effects allow a further reduction in the application rate.The control of a broader spectrum of weeds and grasses, a faster onset of herbicidal action, a longer lasting effect, better control of weeds with only one or a few applications, and an extension of the possible application period. In part, the use of the agents also reduces the amount of harmful ingredients, such as nitrogen or oleic acid, and their input into the soil. The properties and advantages mentioned are desired in practical weed control to keep agricultural crops free of unwanted weeds and thus to secure and / or increase yields qualitatively and quantitatively. The technical standard is significantly exceeded by the new combinations with regard to the described properties. The synergistic effects are observed when the active ingredients (A) and (B) are applied together.However, they can also frequently occur with staggered applications (splitting). It is also possible to apply the herbicides (A) or (Bd) or the herbicidal compositions (A) and (B) in several portions (sequential application). For example, one or more pre-emergence applications can be followed by a post-emergence application, or an early post-emergence application can be followed by a mid- or late post-emergence application. The simultaneous or timely application of the active ingredients of the respective combination, if necessary in several portions, is preferred. However, staggered application of the individual active ingredients of a combination is also possible and can be advantageous in isolation. In the system of application can also be other plant protection products, such as beelsiswpeiise the mentioned other active substances (other herbicides, fungicides, insecticides, acaricides et ucn.)d / or various auxiliary substances, adjuvants and / or fertilizers,be integrated. Depending on the context in which the terms are used, pre-emergence or post-emergence use means the application of the active substances before or after the weeds appear visible above ground, or the application of the active substances against the weeds before or after the crop has emerged. BCS231024-Ausland STR 22 In formula (I) for compounds of the herbicidal active substances (A) and all subsequent formulae, the following definitions apply: The compounds of formula (I) can exist as stereoisomers depending on the linkage of the substituents. For example, if one or more asymmetrically substituted carbon atoms and / or sulfoxides are present, ionomers and diastereomers can occur. Stereoisomers can be separated from the mixtures obtained during production by conventional separation methods, for example by chromatographic separation processes.Stereoisomers can also be selectively prepared by using stereoselective reactions using optically active starting materials and / or auxiliaries. The invention also relates to all stereoisomers and the lower mixtures encompassed by the formula (I) but not specifically defined. For the sake of simplicity, however, reference is always made below to compounds of the formula (I), although both the pure compounds and, where appropriate, mixtures with varying proportions of the isotopic compounds are meant. Depending on the nature of the substituents defined above, these compounds of the formula (I) have acidic properties and can form salts, optionally also internal salts or adducts, with inorganic or organic bases or with metal ions. In addition, the compounds of the formula (I) contain hydroxy, carboxy or other groups exhibiting acidic properties.These compounds can be reacted with bases to form salts. Suitable bases are, for example, hydroxides, carbonates, hydrogen carbonates of alkali and alkali metal ketals, in particular those of sodium, potassium, magnesium and calcium, as well as ammonia, primary, secondary and tertiary amines with C1-(C4)-alkyl groups, mono-, di- and trialkanolamines of C1(-C4)-alkanols, choline and chlorocholine, as well as organic amines such as trialkylamines, morpholine, pyridine or pyridine. These salts are compounds in which the acidic hydrogen is replaced by a cation suitable for agriculture, for example metal salts, in particular alkali metal salts or alkaline earth metal salts, in particular sodium and potassium salts, or ammonium salts, salts with organic amines or quaternary ammonium salts, for example cations of the formula [NRR´R´´R´´, +',] wherein R to R''' each independently represent an organic radical, in particular alkyl, aryl, aralkyl or alkylaryl. Suitable salts include alkylsulfonium and alkylsulfoxonium salts, such as (C1-C4)-trialkylsulfonium and (C1-C4)-trialkylsulfoxonium salts. The compounds of formula (I) can be prepared by annealing with a suitable inorganic or organic acid, such as mineral acids, for example HCl, HBr, HSO4, H3PO4 or HNO3, or organic acids, e.g. B. Carboxylic acids, such as acetic acid, propionic acid, oxalic acid, lactic acid or salicylic acid or sulfonic acids, such as p-toluenesulfonic acid, on a basic group, such as amino, alkylamino, alkylamino, piperidino, morpholino or pyridino, to form salts. These salts contain the conjugate base of the acid as an anion. Suitable substituents which are present in deprotonated form, for exampleSulfonic acids or carboxylic acids, can form internal salts with, in turn, hydrophobic groups, such as amino groups. If a group is polysubstituted by residues, this means that this group is substituted by one or more identical or different ones of the above-mentioned radicals. In all formulas mentioned below, the positions and symbols, unless defined otherwise, have the same meaning as described under the general formula (I) of the herbicides (A). Arrows in a chemical formula indicate the points of contact with the rest of the molecule. In the following, preferred, particularly preferred, and very particularly preferred meanings are described for the individual substituents of the herbicides (A) according to the general formula (I) as shown above. The other substituents of the other herbicides (A) according to the general formula (I), which are not mentioned below, have the above-mentioned meaning.In a first embodiment of the present invention, herbicidally active substances (A) are compounds of the formula (I). where R 1 stands for hydrogen, R 2 represents fluorine, R 3 represents fluorine, R 4 stands for chlorine, bromine, cyano, N2O, BCS231024-Ausland STR 24 R 5 stands for hydrogen, R 6 for hydrogen, fluorine, chlorine, bromine or cyano oh st,t R 7 represents hydrogen, G represents methylene or (methyl)methylene, X represents O (oxygen) or S (sulfur), Y represents O (oxygen), and Q represents one of the groups Q-1 to Q-25 specifically mentioned above. In a second embodiment of the present invention, herbicidally active substances (A) are compounds of the formula (I), where R 1 stands for hydrogen, R 2 represents fluorine, R 3 represents fluorine, R 4 stands for chlorine, bromine, cyano, R 5 stands for hydrogen, R6 stands for hydrogen, fluorine, BCS231024-Ausland STR 25 R 7 represents hydrogen, G represents methylene, X represents O (oxygen), Y represents O (oxygen) and Q represents one of the groups Q-1, Q-2, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-16, Q-18 or Q-t1e9ht specifically mentioned above. In a third embodiment of the present invention, the herbicidal composition contains, in addition to at least one component (B) as above, preferably a compound [component (A)] of the general formula (I) or its agriculturally acceptable salts, where R 1 stands for hydrogen, R 2 represents fluorine, R 3 represents fluorine, R 4 stands for chlorine, R 5 stands for hydrogen, R 6 stands for hydrogen, R 7stands for hydrogen, G stands for methylene, X stands for O (oxygen), Y stands for O (oxygen) BCS231024-Ausland STR 26 and Q stands for the above-mentioned group Q-1. This preferred compound ("A1" hereinafter) is listed below by its structural formula and corresponding IUPAC name. Compound IUPAC Name Structural Formula No. Cyclopropylmethyl (2-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- A1 dihydropyrimidin-1(2H)-yl]phenoxy}phenoxy)acetate The compounds of formula (I) are known from the inorganic application with the application number PCT / EP2023 / 077211 and can be prepared by the processes described. The application rates of the herbicides (A) are in the range from 0.02 to 750 g of active substance per hectare (hereinafter g ai / ha), preferably 0.05 to 40 g ai / ha, in particular 0.25 to 300 g ai / ha.In combinations according to the invention, within the framework of the application rates mentioned, lower application rates of the respective active ingredient are usually required compared to individual applications, preferably 0.02 to 250 g ai / ha, in particular up to 150 g ai / ha, and most preferably 0.2 to 120 g ai / ha. In principle, all active ingredients from subgroups (B1) to (B11) are suitable as combination partners (B) [= component (B) or herbicides (B)]. The designation of the herbicidal active ingredients is largely based on the common name (in English) according to the reference "The Pesticide Manual," 14th Ed., British Crop Protection Convention 2006, abbreviated to "PM," or the chemical name according to the usual nomenclature (C or Chemical Abstracts). However, some herbicides (B) have surprisingly proven to be particularly good combination partners.The preferred, most preferred, and most preferred herbicides (B) are listed below as further embodiments of the present invention. BCS231024-Ausland STR 27 In a fourth embodiment of the present invention, the herbicidally active ingredients (B1) are preferred: (B1.2) Bicyclopyrone, (B1.4) Clethodim, (B1.7) Mesotrione, (B1.8) Pinoxaden, (B1.10) Sethoxydim, (B1.11) Sulcotrione, (B1.14) Tembotrione, (B1.16) Tralkoxydim. Particularly preferred active ingredients from group B1 are (B1.2) bicyclopyrone, (B1.4) clethodim, (B1.7) mesotrione, (B1.8) pinoxaden, (B1.14) tembotrione. Particularly preferred active ingredients from group B1 are (B1.2) bicyclopyrone, (B1.4) clethodim, (B1.7) mesotrione, (B1.14) tembotrione. In a fifth embodiment of the present invention, the herbicidal active ingredients (B2) are preferred: (B2.1) acetochlor, (B2.4) asulam, (B2.6) beflubutamid, (B2.10) chlorimuron, (B2.12) chlorsulfuron, (B2.14) Cloransulam, (B2.17) Diclosulam, (B2.18) Diflufenican, (B2.20) Dimethenamid, (B2.23) Ethoxysulfuron, BCS231024-Ausland STR 28 (B2.24) Flazasulfuron, (B2.25) Florasulam, (B2.26) Flucarbazone, (B2.28) Flufenacet, (B2.29) Flumetsulam, (B2.30) Flupyrsulfuron, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.40) Metolachlor, (B2.41) Metosulam, (B2.42) Metsulfuron, (B2.43) Nicosulfuron, (B2.46) Penoxsulam, (B2.48) Phenmedipham, (B2.56) Propoxycarbazone, (B2.59) Prosulfocarb, (B2.60) Prosulfuron, (B2.62) Pyroxsulam, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.65) Sulfometuron, (B2.66) Sulfosulfuron, (B2.68) Thiencarbazone, (B2.69) Thifensulfuron, (B2.72) Tribenuron, (B2.76) Esprocarb, (B2.78) Tri-allate, (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-methoxy-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-vinyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.81) Icafolin-methyl, (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l-methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, BCS231024-Ausland STR 29 (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)-vinyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)-methyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5-vinyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-m5-ethoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o-fluorphenyl)-5- (trifluormethyl)-4H-1,2-oxazol-5-yl]carbonyl]amincoy]clopent-2-en-1- carboxylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopenten-1-carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-5l)-methyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopenten-1-carboxylat, (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2-ylcarbonyl)cyclopent-2-en- 1-yl]-5-(trifluormethyl)-4H-1,2-oxazol-5-carboxam,id (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4- [(propylsulfonylamino)carbonyl]cyclopent-2-en-1--y5l]-(trifluormethyl)-4H- 1,2-oxazol-5-carboxamid, (B2.92) (1S,4R)-4-[[(5R)-3-(3,5-difluorophenyl)-5e-mthyl-4H-isoxazole-5- carbonyl]amino]cyclopent-2-ene-1-carbonsäure, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl-)[-(3S)-methylsulfinyl]-4- (trifluormethyl)benzamid. Besonders bevorzugt aus der Gruppe B2 sind dieiz hideerbn Wirkstoffe (B2.1) Acetochlor, (B2.18) Diflufenican, (B2.20) Dimethenamid, (B2.24) Flazasulfuron, (B2.28) Flufenacet, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.40) Metolachlor, (B2.43) Nicosulfuron, BCS231024-Ausland STR 30 (B2.48) Phenmedipham, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-methoxy-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-vinyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.81) Icafolin-methyl, (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l-methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)-vinyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)-methyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5-vinyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-m5-ethoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o-fluorphenyl)-5- (trifluormethyl)-4H-1,2-oxazol-5-yl]carbonyl]amincoy]clopent-2-en-1- carboxylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopenten-1-carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-l5)-methyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopenten-1-carboxylat, (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2-ylcarbonyl)cyclopent-2-en- 1-yl]-5-(trifluormethyl)-4H-1,2-oxazol-5-carboxam,id (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4- [(propylsulfonylamino)carbonyl]cyclopent-2-en-1--y5l]-(trifluormethyl)-4H- 1,2-oxazol-5-carboxamid, (B2.92) (1S,4R)-4-[[(5R)-3-(3,5-difluorophenyl)-5e-mthyl-4H-isoxazole-5- carbonyl]amino]cyclopent-2-ene-1-carbonsäure, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl)-[-(3S)-methylsulfinyl]-4- (trifluormethyl)benzamid. BCS231024-Ausland STR 31 Insbesondere bevorzugt aus der Gruppe B2 sinde drbieiz hiden Wirkstoffe (B2.1) Acetochlor, (B2.18) Diflufenican, (B2.20) Dimethenamid, (B2.28) Flufenacet, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.81) Icafolin-methyl. In a sixth embodiment of the present invention, the herbicidally active ingredients (B3) are preferred: (B3.1) Bromoxynil, (B3.4) Ioxynil. Particularly preferred herbicidally active ingredients (B3.1) Bromoxynil are: In a seventh embodiment of the present invention, the herbicidal active ingredients (B4) are preferred: (B4.2) Amitrole, (B4.8) Carfentrazone, (B4.10) Imazamethabenz, (B4.11) Imazamox, (B4.12) Imazapic, (B4.13) Imazapyr, (B4.15) Imazethapyr, (B4.17) Isoxaben, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, (B4.22) Pyrasulfotole, (. B4.25)Pyroxasulfone, BCS231024-Ausland STR 32 (B4.26) Sulfentrazone, (B4.27) Tolpyralate, (B4.28) Topramezone, (B4.33) Flupoxam The following are particularly preferred from Group B4: (B4.8) Carfentrazone, (B4.11) Imazamox, (B4.13) Imazapyr, (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, (B4.22) Pyrasulfotole, ( B4.25) Pyroxasulfone, (B4.26) Sulfentrazone, (B4.27) Tolpyralate Intere besprecht aus der Gruppe B4 sinde drbieiz hiden Wirkstoffte (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, ( B4.25)Pyroxasulfone,(B4.26) Sulfentrazone. In an eighth embodiment of the present invention, the herbicidal active ingredients (B5) are preferred: (B5.1) Aminocyclopyrachlor, (B5.2) Aminopyralid, (B5.3) Benazolin, (B5.5) Bentazone, (B5.7) Bixlozone, (B5.12) Cinidon, (B5.13) Cinmethylin, BCS231024-Ausland STR 33 (B5.14) Clomazone, (B5.20) Ethalfluralin, (B5.21) Ethofumesate, (B5.22) Flamprop, (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.27) Fluridone, (B5.28) Flurochloridone, (B5.29) Flurtamone, (B5.30) Fluthiacet-methyl, (B5.31) Halauxifen, (B5.32) Indanofan, (B5.37) Paraquat, (B5.38) Pelargonic acid, (B5.39) Pendimethalin, (B5.45) Triafamone, (B5.46) Trifluralin, (B5.47) 4-Amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2-carboxylic acid, (B5.48) Cyclopyrimorate, (B5.49) Diquat, (B5.50) Oxaziclomefone. (B5.54) 4-Hydroxy-1-methyl-3-[4-(trifluoromethyl)-2-pyridinyl]-2-imidazolidinone (B5.55) MSMA. Particularly preferred from group B5 are these hidden active ingredients (B5.5) Bentazone, (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.30) Fluthiacet-methyl, (B5.31) Halauxifen, (B5.37) Paraquat, (B5.38) Pelargonic acid, (B5.39) Pendimethalin, (B5.55) MSMA. Particularly preferred active ingredients from group B5 are (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.37) Paraquat, and (B5.39) Pendimethalin. In a ninth embodiment of the present invention, the herbicidally active ingredients (B6) are preferred: (B6.2) clopyralid, (B6.3) dicamba, (B6.4) fluroxypyr, (B6.5) picloram. Particularly preferred from group B6 is the herbicidally active ingredient (B6.3) dicamba. In a tenth embodiment of the present invention, the herbicidally active ingredients (B7) are preferred: (B7.2) bialaphos, (B7.4) glufosinate, (B7.5) glyphosate, (B7.7) sulfosate. Particularly preferred from group B7 are the herbicidally active ingredients (B7.4) glufosinate, (B7.5) glyphosate, (B7.7) sulfosate.Particularly preferred active ingredients from group B7 are (B7.4) Glufosinate, (B7.5) Glyphosate. BCS231024-Ausland STR 35 In an eleventh embodiment of the present invention, the herbicidal active ingredients (B8) are preferred: (B8.1) 2,4-D, (B8.2) 2,4-DB, (B8.3) 2,4-DP, (B8.4) acifluorfen, (B8.5) aclonifen, (B8.8) clodinafop, (B8.11) diclofop, (B8.13) fenoxaprop, (B8.16) fomesafen, (B8.19) lactofen, (B8.20) MCPA, (B8.22) mecoprop, (B8.24) oxyfluorfen, (B8.26) quizalofop, (B8.27) quizalofop-P. Particularly preferred active ingredients from group B8 are (B8.1) 2,4-D, (B8.2) 2,4-DB, (B8.3) 2,4-DP, (B8.4) acifluorfen, (B8.5) aclonifen, (B8.16) fomesafen, (B8.19) lactofen, and (B8.24) oxyfluorfen. Particularly preferred active ingredients from group B8 are (B8.1) 2,4-D, (B8.5) aclonifen, (B8.16) fomesafen, and (B8.24) oxyfluorfen.BCS231024-Ausland STR 36 In a twelfth embodiment of the present invention, the herbicidal active ingredients (B9) are preferred: (B9.3) Butafenacil, (B9.9) Pyrithiobac-sodium, (B9.10) Saflufenacil, (B9.11) Terbacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazine, (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo- 1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate (B9.15) Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)- 3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate (B9.16) methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzylidene}amino]oxy}propanoate (B9.18) Flufenoximacil. Particularly preferred active ingredients from group B9 are (B9.3) butafenacil, (B9.10) Saflufenacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazine, BCS231024-Ausland STR 37 (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo- 1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)- 3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro- 1,2-oxazole-5-carboxylate (B9.16) 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid (B9.17) Methyl-(2RS)-2-{[€-{2-chloro-4- flufenoximacil. In a thirteenth embodiment of the present invention, the herbicidal active ingredients (B10) are preferred: (B10.1) Chlorobromuron, (B10.2) Chlorotoluron, (B10.5) Diuron, (B10.7) Fluometuron (B10.8) Isoproturon, (B10.9) Linuron, (B10.10) Methabenzthiazuron, (B10.11) Metobromuron, (B10.12) Metoxuron, (B10.13) Monolinuron BCS231024-Ausland STR 38 Particularly preferred from group B10 are the following active ingredients: (B10.5) Diuron, (B10.7) Fluometuron (B10.8) Isoproturon, Particularly preferred from group B10 are the herbicidal active ingredients: (B10.5) Diuron, (B10.7) Fluometuron. In a fourteenth embodiment of the present invention, the herbicidal active ingredients (B11) are preferred: (B11.1) Ametryne, (B11.2) Atrazine, (B11.5) Hexazinone, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.12) Simazine, (B11.15) Terbuthylazine, (B11.16) Terbutryne. Particularly preferred from group B11 are the antibiotic active ingredients (B11.2) Atrazine, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.15) Terbuthylazine. Within the scope of the present invention, it is possible to flexibly combine the individual preferred, particularly preferred, and most preferred embodiments.This means that herbicidal compositions comprising (A) one or more compounds of the general formula (I) or their agrochemically acceptable salts [component (A)] and (B) one or more herbicides [component (B)] selected from the group consisting of herbicidally active ingredients (B1) to (B11) are encompassed by the present invention, in which any disclosed, preferred, particularly preferred and most preferred embodiments can be combined with one another as listed above. BCS231024-Ausland STR 39 Some binary compositions comprising (A) or one or more herbicidally active compounds (A) of the general formula (I) or their agrochemically acceptable salts [herbicides (A)], and also a herbicide (B) have surprisingly proven advantageous. The preferred, particularly preferred and most preferred binary systems are listed below as further embodiments of the present invention.In a fifteenth embodiment of the present invention, the composition preferably contains (A) a compound of general formula (I) or its agrochemically acceptable salts [herbicides (A)]. where R 1 stands for hydrogen, R 2 represents fluorine, R 3 represents fluorine, R 4 represents chlorine, bromine or cyano, R 5 stands for hydrogen, R 6 represents hydrogen, fluorine, R 7stands for hydrogen, G stands for methylene, X stands for O (oxygen), BCS231024-Ausland STR 40 Y stands for O (oxygen), Q stands for one of the groups Q-1, Q-2, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-16, Q-18 or Q s-t1e9ht. and (B) a herbicide [component (B)] from the group consisting of (B1.2) bicyclopyrone, (B1.4) clethodim, (B1.7) mesotrione, (B1.8) pinoxaden, (B1.14) tembotrione, (B2.1) acetochlor, (B2.18) diflufenican, (B2.20) dimethenamid, (B2.24) flazasulfuron, (B2.28) flufenacet, (B2.31) foramsulfuron, (B2.34) iodosulfuron, (B2.37) mesosulfuron, (B2.40) metolachlor, (B2.43) nicosulfuron, (B2.48) phenmedipham, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichlorophene)-y5-methoxy-4H-isoxazole-5-carbonyl]amino]tetrahydrofuran-2-carboxylate, (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichlorophene)-y5-vinyl-4H-isoxazole-5-carbonyl]amino]tetrahydrofuran-2-carboxylate, (B2.81) Icafolin-methyl, (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l-methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, BCS231024-Ausland STR 41 (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)-vinyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)-methyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5-vinyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-m5-ethoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o-fluorphenyl)-5-(trifluormethyl)-4H- 1,2-oxazol-5-yl]carbonyl]amino]cyclopent-2-en-1-bcoaxrylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopenten-1-carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-l5)-methyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopenten-1-carboxylat, (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2-ylcarbonyl)cyclopent-2-en-1-yl]-5- (trifluormethyl)-4H-1,2-oxazol-5-carboxamid, (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-[(propsyullfonylamino)carbonyl]cyclopent-2- en-1-yl]-5-(trifluormethyl)-4H-1,2-oxazol-5-carbomxaid, (B2.92) (1S,4R)-4-[[(5R)-3-(3,5-difluorophenyl)-5e-mthyl-4H-isoxazole-5- carbonyl]amino]cyclopent-2-ene-1-carbonsäure, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl-)[-(3S)-methylsulfinyl]-4- (trifluormethyl)benzamid, (B3.1) Bromoxynil, (B4.8) Carfentrazone, (B4.11) Imazamox, (B4.13) Imazapyr, (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, (B4.22) Pyrasulfotole, (B4.25) Pyroxasulfone, (B4.26) Sulfentrazone, (B4.27) Tolpyralate BCS231024-Ausland STR 42 (B5.5) Bentazone, (B5.14) Clomazone (B5.20) Ethalfluralin, (B5.23) Florpyrauxifen (B5.26) Flumioxazin, (B5.30) Fluthiacet-methyl, (B5.31) Halauxifen, (B5.37) Paraquat, (B5.38) Pelargonsäure (B5.55) MSMA (B6.3) Dicamba (B7.2) Bialaphos, (B7.4) Glufosinate, (B7.5) Glyphosate, (B7.7) Sulfosate (B8.1) 2,4-D, (B8.2) 2,4-DB, (B8.3) 2,4-DP, (B8.4) Acifluorfen, (B8.5) Aclonifen, (B8.13) Fenoxaprop, (B8.16) Fomesafen, (B8.19) Lactofen, (B8.24) Oxyfluorfen (B9.3) Butafenacil, (B9.9) Pyrithiobac-sodium, (B9.10) Saflufenacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazin, (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-iftlruoromethyl-2,4-dioxo-1,2,3,4- tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acaett; BCS231024-Ausland STR 43 (B9.15) Ethyl-3-{2-chlor-4-fluor-5-[3-methyl-2,6-dioxo-4-r(itfluormethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihdyro-1,2-oxazol-5-carboxylat (B9.16) 3-[2-Chlor-5-(3,5-dimethyl-2,6-dioxo-4-sulfanylid-e1n,3,5-triazinan-1-yl)-4- fluorphenyl]-5-methyl-4,5-dihydro-1,2-oxazol-5-caornbsäure (B9.17) Methyl (2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzylidene}amino]oxyp}ropanoate (B9.18) Flufenoximacil (B10.5) Diuron, (B10.7) Fluometuron (B10.8) Isoproturon (B11.2) Atrazine, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.15) Terbuthylazine In a sixteenth embodiment of the present invention, the composition preferably contains (A) a compound of the general formula (I) or its agrochemically acceptable salts [herbicides (A)]. where R 1 stands for hydrogen, R 2 represents fluorine, R 3 stands for fluorine, BCS231024-Ausland STR 44 R 4 represents chlorine, bromine or cyano, R 5 stands for hydrogen, R 6 represents hydrogen, fluorine, R 7represents hydrogen, G represents methylene, X represents O (oxygen), Y represents O (oxygen), and Q represents one of the groups specifically mentioned above: Q-1, Q-2, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-16, Q-18 or Q-19; and (B) a herbicide [component (B)] from the group consisting of (B1.2) Bicyclopyrone (CAS 352010-68-5), (B1.4) Clethodim (CAS 99129-21-2), (B1.7) Mesotrione (CAS 104206-82-8), (B1.14) Tembotrione (CAS 335104-84-2) (B2.1) Acetochlor (CAS 34256-82-1), (B2.18) Diflufenican (CAS 83164-33-4), (B2.20) Dimethenamide (CAS 87674-68-8), (B2.24) Flazasulfuron (CAS 104040-78-0), (B2.28) Flufenacet (CAS 142459-58-3), (B2.31) Foramsulfuron (CAS 173159-57-4), (B2.34) Iodosulfuron (CAS 144550-36-7), (B2.37) Mesosulfuron (CAS 208465-21-8), (B2.48) Phenmedipham (CAS 13684-63-4), (B2.64) S-metolachlor (CAS 87392-12-9), BCS231024-Ausland STR 45 (B2.68) Thiencarbazone (CAS 317815-83-1), (B2.81) Icafolin-methyl (CAS 2749998-21-6), (B2.93)2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl-)[-(3S)-methylsulfinyl]-4- (trifluormethyl)benzamid (CAS 2833716-54-2). (B3.1) Bromoxynil (CAS 1689-84-5) (B4.11) Imazamox (CAS 1143-11-32-9), (B4.15) Imazethapyr (CAS 81335-77-5), (B4.18) Isoxaflutole (CAS 141112-29-0), (B4.20) Oxadiazon (CAS 19666-30-9), (B4.21) Pyraflufen-ethyl (CAS 129630-19-9), (B4.25) Pyroxasulfone (CAS 365400-11-9), (B4.26) Sulfentrazone (CAS 122836-35-5) (B5.5) Bentazone (CAS 25057-89-0), (B5.14) Clomazone (CAS 81777-95-9), (B5.20) Ethalfluralin (CAS 55283-68-6), (B5.23) Florpyrauxifen (CAS 943832-81-3), (B5.26) Flumioxazin (CAS 103361-09-7), (B5.37) Paraquat (CAS 1910-42-5) (B6.3) Dicamba (CAS 1918-00-9) (B7.4) Glufosinate (CAS 77182-82-2), (B7.5) Glyphosate (CAS 70901-12-1) (B8.1) 2,4-D (CAS 94-75-7), (B8.5) Aclonifen (CAS 74070-46-5), (B8.16) Fomesafen (CAS 72178-02-0), (B8.24) Oxyfluorfen (CAS 42874-03-3) (B9.3) Butafenacil (CAS 134605-64-4), (B9.9) Pyrithiobac-sodium (CAS 123342-93-8), (CA2S33143-16-8), (B9.10)Saflufenacil (CAS 372137-35-4), (B9.13) Trifludimoxazine (CAS 1258836-72-4) BCS231024-Ausland STR 46 (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-r(itfluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihdyro-1,2-oxazole-5-carboxylate (CAS 1949837-17-5) (B9.16) 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanylide-e1n,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-caornic acid (CAS 2558200-03-4) (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)- 3,6-dihydropyrimidin-1(2H)-yl]benzyliden}amino]oxyp}ropanoate (CAS 2669111-31-1) (B9.18) Flufenoximacil (CAS 2759011-88-4) (B10.5) Diuron (CAS 330-54-1) (B10.7) Fluometuron (CAS 2164-17-2) (B11.2) Atrazine (CAS 1912-24-9), (B11.6) Indaziflam (CAS 950782-86-2) (B11.8) Metribuzin (CAS 21087-64-9), (B11.15) Terbuthylazine (CAS 5915-41-3). Particularly preferred compositions in the sense of the present invention are the compositions as shown in the following table.2f.g1egeführt: Table 2.1: Particularly preferred binary compounds containing (A1) Binary compound (A) Compound (B) Composition Z1-1 A1 2,4-D Z1-2 A1 Acetochlor Z1-3 A1 Aclonifen Z1-4 A1 Atrazine Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6- Z1-5 A1 dihydropyrimidin-1(2H)-yl]phenyl}-5- methyl-4,5-dihydro-1,2-oxazole-5- carboxylate BCS231024-Ausland STR 47 Binary compound (A) Compound (B) Composition 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- Z1-6 A1 fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro- 5-[3-methyl-2,6-dioxo-4- Z1-7 A1 (trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]benzyliden}amino]oxy}propanoate Methyl-(2R)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)- Z1-8 A1 3,6-dihydropyrimidine-1(2H)- yl]benzylidene}amino]oxy}propanoate Z1-9 A1 Bicyclopyrone Z1-10 A1 Bromoxynil Z1-11 A1 Butafenacil Z1-12 A1 Clethodim Z1-13 A1 Dicamba Z1-14A1 Diflufenican Z1-15 A1 Dimethenamid Z1-16 A1 Diuron Z1-17 A1 Florpyrauxifen Z1-18 A1 Flufenacet Z1-19 A1 Flufenoximacil Z1-20 A1 Flumioxazin Z1-21 A1 Fluometuron Z1-22 A1 Fomesafen Z1-23 A1 Foramsulfuron Z1-24 A1 Glufosinate Z1-25 A1 Glyphosate Z1-26 A1 Icafolin-methyl Z1-27 A1 Imazethapyr Z1-28 A1 Indaziflam BCS231024-Ausland STR 48 Binary Compound (A) Compound (B) Composition Z1-29 A1 Iodosulfuron Z1-30 A1 Isoxaflutole Z1-31 A1 Mesosulfuron-Methyl Z1-32 A1 Mesotrione Z1-33 A1 Metribuzin Z1-34 A1 Oxadiazone Z1-35 A1 Oxyfluorfen Z1-36 A1 Paraquat Z1-37 A1 Pendimethalin Z1-38 A1 Pyraflufen-ethyl Z1-39 A1 Pyroxasulfone Z1-40 A1 Rimsulfuron Z1-41 A1 Saflufenacil Z1-42 A1 S-Metolachlor Z1-43 A1 Sulfentrazone Z1-44 A1 Tembotrione Z1-45 A1 Terbuthylanzine Z1-46 A1 Thiencarbazone Z1-47 A1 Tiafenacil Z1-48 A1 Trifludimoxazine 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2- yl)-3-[(S)-methylsulfinyl]-4- Z1-49 A1 (trifluoromethyl)benzamide Z1-50 A1 Phenmedipham Particularly preferred are theCombination Z1s-1 Z b1i-49. Furthermore, the combination according to the invention can be used together with other active ingredients such as the active ingredients mentioned (herbicides, fungicides, insecticides, acaricides, etc.) and / or plant growth regulators or auxiliaries from the group of additives customary in plant protection, such as adjuvants and formulation aids. The combination of plant protection active ingredients containing the active ingredients (fA) and (B) and optionally further active ingredients is referred to here for short as the "herbicide combination." Their BCS231024-Ausland STR 49 application forms such as formulations or tank mixtures represent herbicidal compositions (compositions). The invention therefore also relates to herbicidal compositions which contain the active ingredient combinations according to the invention with additives customary in plant protection, such as adjuvants and formulation aids, and optionally other plant protection active ingredients.The invention also relates to the use or application method using the active ingredient combinations according to the invention as herbicides and plant growth regulators, preferably as herbicides and plant growth regulators with a synergistically effective content of the respective active ingredient combination. The application rates of the herbicides (B) are known in principle and are generally in the range from 0.01 to 4000 g ai / ha, preferably in the range from 0.002 to 3000 g ai / ha, in particular 0.1 to 0.2 g ai / ha. For the active ingredient pelargonic acid (B5.38s) of group (B5), the application rate is in the range from 1 to 100,000 g ai / ha. In the mixtures according to the invention, the application rates mentioned above generally require lower application rates of the respective active ingredient compared to individual applications. For the active ingredients from group (B1), the application rate is preferably in the range from 1 to 250 g ai / ha, in particular in the range from 1 to 150 gu / nhda most preferably in the range of 5 to 100 g ai / ha. For the active ingredients from group (B2) the application rate is preferably in the range of 0.1 to 3000 g ai / ha, in particular in the range of 0.127 to 0.10 g ai / ha, and most preferably in the range of 1 to 2200 g ai / ha. For the active ingredient from group (B3) the application rate is preferably in the range of 10 to 1000 g ai / ha, in particular in the range of 10 to 50 g ai / ha, and most preferably in the range of 10 to 300 g ai / ha. For the active ingredient from group (B4), the application rate is preferably in the range of 1 to 1500 g ai / ha, in particular in the range of 1 to 1 g ai / ha, and most preferably in the range of 1 to 1000 g ai / ha. BCS231024-Ausland STR 50 For the active ingredient from group (B5), except phenargonic acid (B5.38), the application rate is preferably in the range of 1 to 1500 g ai / ha, in particular in the range of 1 to 1000 g ai / ha, and most preferably in the range of 1 to600 g / h ai For pelargonic acid (B.5.38) the application rate is preferably 1 to 100,000 g ai / ha, more preferably 1 to 40,000 g ai / ha and in particular in the range from 1 to 30,000 g ai / ha. For the active ingredient from group (B6) the application rate is preferably in the range from 1 to 1000 g ai / ha, in particular in the range from 1 to 80 ai / ha, and most preferably in the range from 5 to 600 g ai / ha. For the active ingredient from group (B7) the application rate is preferably in the range from 20 to 3000 g ai / ha, in particular in the range from 20 to 20 g ai / ha, and most preferably in the range from 30 to 1300 g ai / ha. For the active ingredient from group (B8), the application rate is preferably in the range of 1 to 1500 g ai / ha, in particular in the range of 1 to 1 g ai / ha and most preferably in the range of 1 to 800 g ai / ha. For the active ingredient from group (B9), the application rate is preferably in the range of 0.1 to 500 g ai / ha, in particular in the range of 0.1to 25 g ai / ha, and most preferably in the range of 0.2 to 100 g ai / ha. For the active ingredient from group (B10), the application rate is preferably in the range of 20 to 2500 g ai / ha, in particular in the range of 20 to 100 g ai / ha, and most preferably in the range of 20 to 1500 g ai / ha. For the active ingredient from group (B11), the application rate is preferably in the range from 5 to 2000 g ai / ha, in particular in the range from 5 to 1 g ai / ha, and most preferably in the range from 5 to 1000 g ai / ha. The ratios (A):(B) based on the amount are, depending on the effective application rates, generally in the range from 1:100 to 3000:1, preferably 1:80000 to 2000:1, in particular in the range from 1:15000 to 1000:1. For the active ingredients from groups (B1) to (B1i1n)ds, the preferred weight ratios (A):(B) are as follows: BCS231024-Ausland STR 51 (A):(B1) preferably in the range of 150:1 to 10:02.5, in particular 24:1 to 1:400; (A):(B2)preferably in the range from 1500:1 to 510:040, in particular 120:1 to 1:9000; (A):(B3) preferably in the range from 15:1 to 1:08.5, in particular 12:1 to 1:1200; (A):(B4) preferably in the range from 150:1 to 10:020, in particular 120:1 to 1:4000; (A):(B5) preferably in the range from 150:1 to 10:0107, in particular 120:1 to 1:2400; (A):(B6) preferably in the range from 150:1 to 15:0103, in particular 24:1 to 1:2400; (A):(B7) preferably in the range from 7:1 to 1:103.5, in particular 4:1 to 1:5200; (A):(B8) preferably in the range from 150:1 to 10:0107, in particular 120:1 to 1:3200; (A):(B9) preferably in the range from 1500:1 to 210:04, in particular 600:1 to 1:400; (A):(B10) preferably in the range from 7:1 to 1:0304.0, in particular 6:1 to 1:6000; (A):(B11) preferably in the range from 1500:1 to 45:10:0, in particular 600:1 to 1:400. The herbicidal compositions according to the invention can also be combined with other herbicides and plant growth regulators (= active ingredients (C*)to supplement the spectrum of effects, for example. As combination agents for the compounds according to the invention in mixture formulations or in tank mixes, known active ingredients which are based on the inhibition of, for example, acetolactate synthase, acetyl-CoA carboxylase, cellulose synthase, enolpyruvylshikimate-3-phosphate synthase, glutamyl phosphate synthase, p-hydroxyphenylpyruvate dioxygenase, phytoene desaturase, photosystem Io,s pyhsotem II, protoporphyrinogen oxidase can be used, as they are known, for example, from Weed Research 26) (1494816-445 or "The Pesticide Manual", 14th edition, The British Crop Protection Council and the Royal Society of Chemistry, 2006, the corresponding "e-Pesticide Manual Version 406 (2)" and literature cited therein. Other trade names and common names are listed in the "pCeondium of Pesticide Common Names" (available online at http: / / w.walwanwood.net / pesticides). Known herbicides that can be used with the inventiveThe following active ingredients can be mentioned, for example (Note: The compounds are to be identified either by the "common name" according to the International Organization for Standardization (ISO) or by the chemical name, BCS231024 - Foreign STR 52, if applicable together with a common code number benzene tc) and always include all application forms such as acids, salts, esters and isomers as well as stereoisomers and optical isomers. One and sometimes several application forms are mentioned: acifluorfen, allidochlor, amidochlor, 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methylphenyl)-5-fluoropyridine-2-carboxylic acid, ammonium sulfam, a butyl furesate, bensulide, bipyrazone, bromobutide, busoxinone, butenachlor, butylate, b ceanmdichlor, chlorfenac, chlrofenac-ammonium, chlorfenac-sodium, chlorfenprop, chlrofenprop-mel,th chylorflurenol, chlorflurenol-methyl, chlorophthalim, clacyfos, cumyluron, cyanamide, lo caycte, cyprazine, dalapon, dalapon-calcium, dalapon-magnesium,dalapon-sodium, dazomet, daz-soomdeiutm, n-decanol, detosyl-pyrazolate (DTP), 2-(2,4-dichlorobenzyl)-4,4-dimethyl-1,2-oxazolid3in-o-ne, 2-(2,5-dichlorobenzyl)-4,4-dimethyl-1,2- oxazolidin-3-one, dichlorprop, dichlorprop-butot dyli,chlroprop-dimethylammonium, dichhlorprop- etexyl, dichlorprop-ethylammonium, dichlorprop-istyol,c dichlorprop-methyl, dichlorprop-postassium, dichlorprop-sodium, dichlorprop-P, dichlorprop-Pm-deithylammonium, dichlorprop-P-etexyl, dichlorprop-P-potassium, dichlorprop-sodium, difoeqnuzat, difenzoquat-metilsulfate, dimepiperate,dimesulfazet, dimetrasulfuron, dinoterb, dinotecrbe-ta te, diphenamid, DNOC, DNOC-ammonium,DNOC-potassium, DNOC-sodium, endothal, endothaml-dmiaonium, endothal-dipotassium, endothal- disodium, Epyrifenacil, EPTC, ethiozin, etobenza,n Fi-d5231, i.e. N-[2-Chlor-4-fluor-5-[4-(3- fluorpropyl)-4,5-dihydro-5-oxo-1H-tetrazol-1-yl]-pehnyl]-ethansulfonamid, F-7967, i.e.3-[7-Chlor-5-fluor-2-(trifluormethyl)-1H-benzimidazol-4-yl]-1-mtheyl-6-(trifluormethyl)pyrimidin-2,4(1H,3H)-dion, fenoxasulfone, fenpyrazone, fluchloralin, fluren folul,renol-butyl, -dimethylammonium und -methyl, flupropanate, flupropanate-sdium, fosamine, fosaem-aimnmonium, H-9201, i.e. O-(2,4-Dimethyl-6- nitrophenyl)-O-ethyl-isopropylphosphoramidothio haat,losulfuron, HW-02, i.e.1- (Dimethoxyphosphoryl)-ethyl-(2,4-dichlorphenoxy)atacte, karbutilate, KUH-043, i.e.3-({[5- (Difluormethyl)-1-methyl-3-(trifluormethyl)-1H-pyrzaol-4-yl]methyl}sulfonyl)-5,5-dimethyl-4,5- dihydro-1,2-oxazol, ketospiradox, ketospiradox-psosituam, mefluidide, mefluidide-diolamine, mefluidide-potassium, methabenzthiazuron, metamth,i mopeyrsulfuron, methiozolin, methyl isothiocyanate, molinate, monosulfuron, monosulnfu-mroethyl, MT-5950, i.e. N-[3-chlor-4-(1- methylethyl)-phenyl]-2-methylpentanamid, NGGC-01 na1,propamide, NC-310, i.e.4-(2,4- Dichlorbenzoyl)-1-methyl-5-benzyloxypyrazol, orbeanrbc, pebulate, pentachlorphenol,petroleum oils, primisulfuron, prodiamine, pyribambenz, pyribamb-eisnozpropyl, pyribambenz-propyl, pyributicarb, quinoclamine, SL-261, SYP-249, i.e.1-Ethoxy-3-myel-t1h-oxobut-3-en-2-yl-5-[2-chlor-4- (trifluormethyl)phenoxy]-2-nitrobenzoat, SYP-30.0e,. i 1-[7-Fluor-3-oxo-4-(prop-2-in-1-yl)-3,4- dihydro-2H-1,4-benzoxazin-6-yl]-3-propyl-2-thioxoiidmazolidin-4,5-dion, TCA (Trifluoressigsäure), TCA-ammonium, TCA-calcium, TCA-ethdyl, TCA-magnemsi,u TCA-sodium, terbucarb, thiobencarb, tolpyralate, urea sulfate, vernolate, XDE-848, Z8J6-20, i.e.3,4-Dichlor-N-{2-[(4,6-dimethoxypyrimid-in 2-yl)oxy]benzyl}anilin, 3-(2-chloro-4-fluoro-5-(3-methyl-2,6-dioxo-4-trifluoromethyl-3,6- dihydropyrimidin-1 (2H)-yl)phenyl)-5-methyl-4,5-dyihdroisoxazole-5-carboxylic acid ethyl ester, 3- BCS231024-Ausland STR 53chloro-2-[3-(difluoromethyl)isoxazolyl-5-yl]pheny5l- chloropyrimidin-2-yl ether, 2-(3,4-dimethoxyphenyl)-4-[(2-hydroxy-6-oxocyclohex-1-e-ny-l1)carbonyl]-6-methylpyridazin-32(H)-one, 2-({2-[(2-methoxyethoxy)methyl]-6-methylpyridin-3-ycl}arbonyl)cyclohexane-1,3-dione, (5-hydroxy-1- methyl-1H-pyrazol-4-yl)(3,3,4-trimethyl-1,1-dioxid-2o,3-dihydro-1-benzothiophen-5-yl)methanone, 1- methyl-4-[(3,3,4-trimethyl-1,1-dioxido-2,3-dihydr1o--benzothiophen-5-yl)carbonyl]-1H-pyrazol-5-yl propane-1-sulfonate, 1-{2-chloro-3-[(3-cycloprop5y-lh-ydroxy-1-methyl-1H-pyrazol-4-yl)carbonyl]-6- (trifluoromethyl)phenyl}piperidin-2-one, 4-{2-chlor-3-[(3,5-dimethyl-1H-pyrazol-1-yl)methyl]-4- (methylsulfonyl)benzoyl}-1-methyl-1H-pyrazol-5-yl,31-dimethyl-1H-pyrazole-4-carboxylate; cyanomethyl 4-amino-3-chloro-5-fluoro-6-(7-fluoroH--1indol-6-yl)pyridine-2-carboxylate, prop-2-yn-1- yl 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-y6l)pyridine-2-carboxylate, methyl 4-amino-3- chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine2--carboxylate, benzyl 4-amino-3-chloro-5-fluoro-6- (7-fluoro-1H-indol-6-yl)pyridine-2-carboxylate, eytlh 4-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2-carboxylate, methyl 4-amino-3-cholo-5r-fluoro-6-(7-fluoro-1-isobutyryl-1H-indol-6- yl)pyridine-2-carboxylate, methyl 6-(1-acetyl-7-oflruo-1H-indol-6-yl)-4-amino-3-chloro-5- fluoropyridine-2-carboxylate, methyl 4-amino-3-crholo-6-[1-(2,2-dimethylpropanoyl)-7-fluoro-1H- indol-6-yl]-5-fluoropyridine-2-carboxylate, meth 4yl-amino-3-chloro-5-fluoro-6-[7-fluoro-1- (methoxyacetyl)-1H-indol-6-yl]pyridine-2-carboxyela,t potassium 4-amino-3-chloro-5-fluoro-6-(7- fluoro-1H-indol-6-yl)pyridine-2-carboxylate, sodiu 4m-amino-3-chloro-5-fluoro-6-(7-fluoro-1H-indol- 6-yl)pyridine-2-carboxylate, butyl 4-amino-3-chlo-5ro-fluoro-6-(7-fluoro-1H-indol-6-yl)pyridine-2- carboxylate, 4-hydroxy-1-methyl-3-[4-(trifluoromeytlh)pyridin-2-yl]imidazolidin-2-one, 3-(5-tert-buty-l 1,2-oxazol-3-yl)-4-hydroxy-1-methylimidazolidin-2n-oeWenn die jeweilige Bezeichnung (common name) meh Freor men des Wirkstoffes umfasst, ist mit derBezeichnung die kommerziell erhältliche Form bevuogrtz definiert. Jeder derThe further active ingredients mentioned (= active ingredient (Cf*), (C1*), (C2*) etc.) can then preferably be combined with one of the two-combination products according to the invention, according to the scheme (A)+(B)+(C*) or according to the scheme (A)+(B)+(C)+(C2*) etc. The quantities given are application rates (g ai / hara = gm active substance per hectare) and thus also define the proportions of a cinema formulation, a pre-mix, a tank mix or a sequential application of the active ingredients. The combinations can be used both pre-emergence and post-emergence. This applies to both pre- and post-emergence in relation to the weeds and also to the selective control of the weeds for the pre- or post-emergence of the crop plants. BCS231024-Ausland STR 54 also allows for mixed forms, e.g., the control of harmful plants during their pre- or post-emergence phase.Of interest is the selective control of weeds in crops of useful and ornamental plants. Although the herbicides (A) and (B) exhibit very good to sufficient selectivity in many crops, phytotoxicities can in principle occur in some crops, and especially in the case of mixtures with other herbicides that are less active. In this regard, combinations of herbicides (A) and (B) are of particular interest, which contain the herbicides combined according to the invention and one or more safeners. The safeners, which are used in an antidote-effective concentration, reduce the phytotoxic side effects of the herbicides / pesticides used, e.g. B. in economically important crops such as cereals (wheat, wheat, corn, rice, millet), sugar beet, sugar cane, rapeseed, cotton and soybeans, preferably fermented cereals. Combination partners for the fungicide combinations according to the invention areFor example, the following safeners are suitable: S1) Compounds from the group of heterocyclic rebro Cnaic acid derivatives: S1 a ) Compounds of the type dichlorophenylpyrazoli-nc-a3rbonic acid (S a )1, preferably compounds such as 1-(2,4-Dichlorophenyl)-5-(ethoxycarbonyl)-5-methyl-lp-2yrazoline-3-carboxylic acid, 1-(2,4-Dichlorophenyl)-5-(ethoxycarbonyl)-5-methyl-lp-2yrazoline-3-carboxylic acid ethyl ester (S1-1) ("Mefenpyr-diethyl"), and related compounds as described in WO-A-91 / 07874; S1 b ) Derivatives of dichlorophenylpyrazolecarboxylic acid b ) (,S preferably compounds such as 1-(2,4-dichlorophenyl)-5-methylpyrazole-3-carboxylic acid ethyl ester (S1-2), 1-(2,4-dichlorophenyl)-5-isopropylpyrazole-3-carboxylic acid ethyl ester (S1-3), 1-(2,4-dichlorophenyl)-5-(1,1-dimethylethyl)pyraz-3o-1carboxylic acid ethyl ester (S1-4) and related compounds as described in EP-A-333131 E and EP-A-269806; S1 c ) Derivatives of 1,5-diphenylpyrazole-3-carboxylic acidc ) (,S preferably compounds such as 1-(2,4-dichlorophenyl)-5-phenylpyrazole-3-carboxylic acid threyl ester (S1-5), 1-(2-chlorophenyl)-5-phenylpyrazole-3-carboxylic acid methyl ester (S1-6) and related compounds as described, for example, in EP-A5-25648; BCS231024-Ausland STR 55 S1 d ) Compounds of the triazolecarboxylic acid type d ) (,S preferably compounds such as fenchlorazole(ethyl ester), ie 1-(2,4-dichlorophle)-n5y-trichloromethyl-(1H)-1,2,4-triazole-3-carboxylic acid ethyl ester (S1-7), and related compounds as described in EP-A-174562 and EP-A-346620; S1 e ) Compounds of the type 5-benzyl- or 5-Phe2n-yisl-oxazoline-3-carboxylic acid, or 5,5-diphenyl-2-isoxazoline-3-carboxylic acid( eS),1 preferably compounds such as 5-(2,4-dichlorobenzyl)-2-isoxazoline-3-carboxylic acid ethyl ester (S1-8) or 5-phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (S1-9d) and related compounds as described in WO-A-91 / 08202, or 5,5-diphenyl-2-isoxazoline-3-carboxylic acid (S1-10) or 5,5-diphenyl-2-isoxazoline-3-carboxylic acid ethyl ester (S1-12) (Isoxadifen-ethyl) or -n-propyl ester (S1-12) or 5-(4-fluorophenyl-5-(1-p)phenyl-2-isoxazoline-3-carboxylic acid ethyl ester (S1-13), as described in patent application WO-A-95 / 07897. S1 f ) Compounds of the triazolyloxyacetic acid type f(),S preferably compounds such as methyl {[1,5-bis(4-chloro-2-fluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate (S1-14) or {[1,5-bis(4-chloro-2-fluorophenyl)-1H-1,2,4-triazol-3-yl]y}acetic acid (S1-15) or methyl {[5-(4-chloro-2-fluorophenyl)-1-(2,4-difluorophenyl)-1-1H,2,4-triazol-3-yl]oxy}acetate (S1-16) or {[5-(4-chloro-2-fluorophenyl)-1-(2,4-difluoropheny-l1)H-1,2,4-triazol-3-yl]oxy}acetic acid (S1-17) or Methyl {[1-(4-chloro-2-fluorophenyl)-5-(4-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}acetate (S1-18) or {[1-(4-chloro-2-fluorophenyl)-5-(2,4-difluorophenyl)-1H-1,2,4-triazol-3-yl]oxy}}-acetic acid (S1-19), as described in patent application WO2021105101. S2) Compounds from the group of 8-quinoline hydroxy acids (S2): S2 a ) Compounds of the type 8-quinolinoxyacetic acid (uSr2e a), preferably (5-chloro-8-quinolinoxy)acetic acid (1-methylhexyl)ester ("Cloquintocet-mexyl") (S2-1), (5-chloro-8-quinolinoxy)acetic acid (1,3-dimethyl--b1u-yl)-ester (S2-2), (5-chloro-8-quinolinoxy)acetic acid 4-allyl-oxy-butylester (S2-3), (5-chloro-8-quinolinoxy)acetic acid 1-allyloxy-prop-y-12ester (S2-4), (5-chloro-8-quinolinoxy)acetate ethyl ester (S2-5), (5-chloro-8-quinolinoxy)acetate methyl ester (S2-6) (5-chloro-8-quinolinoxy)acetate allyl ester (S2-7), (5-Chloro-8-quinolinoxy)acetic acid 2-(2-propylidemnioxy)-1-ethyl ester (S2-8), (5-Chloro-8-quinolinoxy)acetic acid 2-oxo-prop-1-yl ester (S2-9) and related compounds as described in EP-A-86750, EP-A-94349 and EP-A-19173d6er o EP-A-0492366, BCS231024-Ausland STR 56 and (5-Chloro-8-quinolinoxy)acetic acid (S2-10)r,e the hydrates and salts, for example their lithium, sodium, potassium, calcium, magnesium, aluminum, iron, ammonium, quaternary ammonium, sulfonium,or phosphonium zea as described in WO-A-2002 / 34048; S2, b ) Compounds of the type (5-chloro-8-quinolinoxya)lmonic acid (S b2), preferably compounds such as (5-chloro-8-quinolinoxy)malonic acid ethyl ester, (5-chloro-8-quinolinoxy)malonic acid diallyl ester, (5-chloro-8-quinolinoxy)malonic acid methyl ethyl ester and related compounds as described in EP-A-0582198.S3) Active ingredients of the dichloroacetamide type (S3ie), which are frequently used as pre-emergence safeners (soil-acting safeners), such as. B "Dichlormid" (N,N-diallyl-2,2-dichloroacetamide) (S31-), "R-29148" (3-dichloroacetyl-2,2,5-trimethyl-1,3-oxoalizdin) from Stauffer (S3-2), "R-28725" (3-dichloroacetyl-2,2,-dimethyl-1,3-oxaizdoinl) from Stauffer (S3-3), "Benoxacor" (4-dichloroacetyl-3,4-dihydro-3-methyHl--21,4-benzoxazine) (S3-4), "PPG-1292" (N-allyl-N-[(1,3-dioxolan-2-yl)-methyld]-ichloroacetamide) from PPG Industries (S3-5), "DKA-24" (N-allyl-N-[(allylaminocarbonyl)methyl]-dichloroacetamide) from Sagro-Chem (S3-6), "AD-67" or "MON 4660" (3-dichloroacetyl-1-oxa-3-a-zspiro[4,5]decane) from Nitrokemia orMonsanto (S3-7), "TI-35" (1-Dichloroacetyl-azepane) from TRI-Chiecmal RT (S3-8), "Diclonon" (Dicyclonone) or "BAS145138" or "LAB415138" (S3-9) ((RS)-1-Dichloroacetyl-3,3,8a-trimethylperhydropyrrol[o1,2-a]pyrimidin-6-one) from BASF, "Furilazol" or "MON 13900" ((RS)-3-Dichloroacetyl--(2-furyl)-2,2-dimethyloxazolidine) (S3-10), as well as its (R)-isome (Ser3-11). S4) Compounds from the class of acylsulfonams (Sid4e): S4. a ) N-acylsulfonamides of the formula (S a )4 and their salts as described in WO-A-97 / 45016, wherein BCS231024-Foreign STR 57 R A 1 (C1-C6)alkyl, (C3-C6)cycloalkyl, where the last two radicals are A ch substituents from the group halogen1-,C (C4)alkoxy, (C1-C6)haloalkoxy and (C1-C4)alkylthio and in the case of cyclic radicals also by (C1-C4)alkyl and (C1-C4)haloalkyl; RA 2Halogen, (C1-C4)alkyl, (C1-C4)alkoxy, CF3; mA is 1 or 2; vA is 0, 1, 2 or 3; S4 b ) Compounds of the type 4-(benzoylsulfamoyl)baemnzides of the formula (S b )4 and their salts as described in WO-A-99 / 16744, where R B 1 , R B 2 independently hydrogen1,-C (C6)alkyl, (C3-C6)cycloalkyl, (C3-C6)alkenyl, (C3-C6)alkynyl, R B 3 Halogen, (C1-C4)alkyl, (C1-C4)haloalkyl or (C1-C4)alkoxy and mB 1 or 2, e.g. those wherein RB 1 = Cyclopropyl, RB 2 = hydrogen and (BR 3 ) = 2-OMe is ("Cyprosulfamide", S4-1), RB 1 = Cyclopropyl, RB 2 = hydrogen and (BR 3 ) = 5-Cl-2-OMe is (S4-2), RB 1 = Ethyl, RB 2 = hydrogen and (BR 3 ) = 2-OMe is (S4-3), RB 1 = Isopropyl, RB 2 = hydrogen and (BR 3 ) = 5-Cl-2-OMe is (S4-4) and RB 1= Isopropyl, RB 2 = hydrogen and (BR 3 ) = 2-OMe is (S4-5); BCS231024-Abroad STR 58 S4 c ) Compounds from the class of benzoylsulfamhoeynlpylureas of the formula (S c ),4 as described in EP-A-365484, where RC 1 , RC 2 independently of one another hydrogen1,-C (C8)alkyl, (C3-C8)cycloalkyl, (C3-C6)alkenyl, (C3-C6)alkynyl, RC 3 halogen, (C1-C4)alkyl, (C1-C4)alkoxy, CF3 and m is C 1 or 2; for example 1-[4-(N-2-methoxybenzoylsulfamoyl)phenyl]-3-methylurea, 1-[4-(N-2-methoxybenzoylsulfamoyl)phenyl]-3,3-dimethylurea, 1-[4-(N-4,5-dimethylbenzoylsulfamoyl)phenyl]-3-methylurea;S4 d ) Compounds of the type N-phenylsulfonylterepahlathmide of the formula (S d )4 and their salts, which are known for example from CN 101838227, where RD 4 Halogen, (C1-C4)alkyl, (C1-C4)alkoxy, CF3; mD 1 or 2; RD 5hydrogen, (C1-C6)alkyl, (C3-C6)cycloalkyl, (C2-C6)alkenyl, (C2-C6)alkynyl, (C5-C6)cycloalkenyl. S5) Active ingredients from the class of hydroxyaromatic aromatic-aliphatic carboxylic acid derivatives (S5), e.g. BCS231024-Ausland STR 59 3,4,5-triacetoxybenzoic acid ethyl ester, 3,5-dimeyt-h4o-hydroxybenzoic acid, 3,5-dihydroxybenzoic acid, 4-hydroxysalicylic acid, 4-fluorocyclic acid, 2-hydroxycinnamic acid, 2,4-dichlorocinnamic acid, as described in WO-A-2004 / 0846 W310, -A-2005 / 015994, WO-A- 2005 / 016001. S6) Active ingredients from the class of 1,2-dihydroquinoxalin-2-ones (S6), e.g. 1-methyl-3-(2-thienyl)-1,2-dihydroquinoxalin-2-one, 1-methyl-3-(2-thienyl)-1,2-dihydroquinoxalin-2-thione, 1-(2-aminoethyl)-3-(2-thienyl)-2-dihydroquinoxalin-2-one hydrochloride, 1-(2-methylsulfonylaminoethyl)-3-(2-thienyl)-1,2-hydroquinoxalin-2-one, as described in WO-A-2005 / 112630. S7) Compounds from the class of diphenylmethanesulfonic acid derivatives (S7), e.g.Diphenylmethoxyacetic acid methyl ester (CAS Reg. 1N8r.548-19-9) (S7-1), diphenylmethoxyacetic acid ethyl ester or diphenylmethoxyacetic acid as described in WO-A-98 / 38856. S8) Compounds of formula (S8) as described in WO-A-098 / 27049. where the symbols and indices have the following meaning: RD 1 is halogen, (C1-C4)alkyl, (C1-C4)haloalkyl, (C1-C4)alkoxy, (C1-C4)haloalkoxy, RD 2 is hydrogen or (1C-C4)alkyl, RD 3is hydrogen, (C1-C8)alkyl, (C2-C4)alkenyl, (C2-C4)alkynyl, or aryl, where each of the aforementioned C-containing radicals is unsubstituted or substituted by one or more, preferably up to three identical or different radicals from deprp Ge,ru consisting of halogen and alkoxy; or their salts, nD is an integer from 0 to 2. S9) Active ingredients from the class of 3-(5-tetrazolylcarboxyl)-2-quinolones (S9), e.g. 1,2-dihydro-4-hydroxy-1-ethyl-3-(5-tetrazolylcarboxyl)n-2-quinolone (CAS Reg. No.: 219479-18-2), 1,2-dihydro-4-hydroxy-1-methyl-3-(5-tetrazolylcarboxyl)-2-quinolone (CAS Reg. No. 95855-00-8), as described in WO-A-1999 / 000020. BCS231024-Ausland STR 60 S10) Compounds of the formulas (S a )1 or (S10 b ), as described in WO-A-2007 / 023719 and WO-A-2007 / 062437, where R E 1 Halogen, (C1-C4)alkyl, methoxy, nitro, cyano, C3F, OCF3Y E , Z E independently O or S, nE an integer from 0 to 4, R E 2 (C1-C 16 )alkyl, (C2-C6)alkenyl, (C3-C6)cycloalkyl, aryl; Benzyl, halobenzyl, R E 3hydrogen or (1C-C6)alkyl. S11) Active ingredients of the oxyimino compound type Sn1 (1), which are known as seed dressings, such as B. "Oxabetrinil" ((Z)-1,3-dioxolan-2-ylmethoxyimino(phenyl)acetonitrile) (S11-1), which is known as a seed dressing safener for millet against damage from mehtlol ra, "Fluxofenim" (1-(4-chlorophenyl)-2,2,2-trifluoro-1-heptone-O-(1,3-dioxolan-2-ylmethyl)-oxime) (S11-2), which is known as a seed dressing safener for millet compared to metolachlor, and "Cyometrinil" or "CGA-43089" ((Z)-cyanomethoxyimino(phenyl)acetonitrile) (S11-3), which is known as a seed dressing safener for millet against damage from mehtlol ra. S12) Active ingredients from the class of isothiochromes (oSn12), such as methyl [(3-oxo-1H-2-benzothiopyran-4(3H)-ylidene)methoxy]acetate (CAS-R.Nerg. 205121-04-6) (S12-1) and related compounds from WO-A-1998 / 13361.S13) One or more compounds from group): (S13 BCS231024-Ausland STR 61 "Naphthalic anhydride" (1,8-naphthalenedicarboxylic acid rheohydride) (S13-1), which is known as a seed dressing safener for maize against damage from thiocarbamate herbicides, "Fenclorim" (4,6-dichloro-2-phenylpyrimidine) (S13-,2-d), which is known as a safener for pretilachlor in sown rice, "Flurazole" (benzyl 2-chloro-4-trifluoromethyl-1,3-ithazole-5-carboxylate) (S13-3), which is known as a seed dressing safener for millet against damage from aolrac and metolachlor, "CL 304415" (CAS Reg. No. 31541-57-8) (4-Carboxy-3,4-dihydro-2H-1-benzopyran-4-acetic)ä (uSre13-4) from American Cyanamid, which is known as a safener for corn against pests in oviodazolinones, "MG 191" (CAS Reg. No. 96420-72-3) (2-Dichlorometh2y-lm- methyl-1,3-dioxolane) (S13-5) from Nitrokemia, which is known as a safener for corn, "MG 838" (CAS Reg. No. 133993-74-5) (2-propenyl 1-oxa-4-azaspiro[4.5]decan-4-carboodaithiat)i (S13-6) from Nitrokemia "Disulfoton" (O,O-Diethyl S-2-ethylthioethyl phosphorithioate) (S13-7), "Dietholate" (O,O-Diethyl-O-phenylphosphorothioate (S13-8), "Mephenate" (4-Chlorophenyl methylcarbamate) (S13-9).S14) Active ingredients which, in addition to a herbicidal effect on harmful plants, also have a safener effect on crops such as rice, such as"Dimepiperate" or "MY-93" (1-methyl-1-phenylethyl-piperidine-1-carbothioate), known as a safener for rice against damage from the herbicide Methylurea, "Daimuron" or "SK 23" (1-(1-methyl-1-phenyleth-yl)-p-tolylurea), known as a safener for rice against damage from the herbicide Imazosulfuron, "Cumyluron" = "JC-940" (3-(2-chlorophenylmethyl)-1-(methyl-1-phenylethyl)urea, see JP-A-60087254), known as a safener for rice against certain herbicides, "Methoxyphenone" or "NK 049" (3,3'-Dimethyl-4-methyl-benzophenone), which is known as a safener for rice against damage caused by some herbicides, "CSB" (1-Bromo-4-(chloromethylsulfonyl)benzene) from Kmuiai, (CAS Reg. No. 54091-06-4), which is known as a safener against damage caused by some herbicides in b Reekiasnnt. BCS231024-Ausland STR 62 S15) Compounds of the formula (S15) or their derivatives,. as described in WO-A-2008 / 131861 and WO-A-2008 / 13018, wherein RH 1a (C1-C6)haloalkyl radical and R H 2 hydrogen or halogen and R H 3 , R H 4 independently of each other hydrogen1,-C (C 16 )Alkyl, (C2-C 16 )alkenyl or (C2-C 16)Alkynyl, where each of the last-mentioned 3 radicals is unsubstituted or substituted by one or more radicals from the group consisting of halogen, hydroxy, cyano-, C(4C)alkoxy, (C1-C4)haloalkoxy, (C1-C4)alkylthio, (C1-C4)alkylamino, di[(C1-C4)alkyl]amino, [(C1-C4)alkoxy]carbonyl, [(C1-C4)haloalkoxy]carbonyl, (C3-C6)cycloalkyl, which is unsubstituted or substituted, phenyl, which is unsubstituted or substituted, and heterocyclyl, which is unsubstituted or substituted, or (C3-C6)cycloalkyl, (C4-C6)cycloalkenyl, (C3-C6)cycloalkyl which is condensed on one side of the ring with a 4 to 6-membered saturated or unsaturated carbocyclic ring, or (C4-C6)cycloalkenyl which is condensed on one side of the ring with a 4 to 6-membered saturated or unsaturated carbocyclic ring, wherein each of the latter 4 radicals is unsubstituted or substituted by one or more radicals from the group halogen, hydroxy, cyano-, C(4C)alkyl, (C1-C4)haloalkyl, (C1-C4)alkoxy,(C1-C4)haloalkoxy, (C1-C4)alkylthio, (C1-C4)alkylamino, di[(C1-C4)alkyl]amino, [(C1-C4)alkoxy]carbonyl, [(C1-C4)haloalkoxy]carbonyl, (C3-C6)cycloalkyl, which is unsubstituted or substituted, phenyl, which is unsubstituted or substituted, and heterocyclyl, which is unsubstituted or substituted, is substituted, BCS231024-Ausland STR 63 or R, H 3 (C1-C4)-alkoxy, (C2-C4)alkenyloxy, (C2-C6)alkynyloxy or (C2-C4)haloalkoxy and RH 4denotes hydrogen or (C-C4)-alkyl or RH3 and RH4 together with the directly bonded N atom form an eight-membered heterocyclic ring which, in addition to the N atom, may also contain hetero ring atoms, preferably up to two further hetero ring atoms from the group consisting of Nun, Os and which is unsubstituted or substituted by one or more radicals from the group consisting of halogen, cyano, nitro, (C-C4)alkyl, (C-C4)haloalkyl, (C-C4)alkoxy, (C-C4)haloalkoxy and (C-C4)alkylthio. S16) Active ingredients which are primarily used as herbicides but also have a safener effect on crops, e.g. E.g. (2,4-Dichlorophenoxy)acetic acid (2,4-D), (4-Chlorophenoxy)acetic acid, (R,S)-2-(4-Chloro-o-tolyloxy)propionic acid (Mecopro, p) 4-(2,4-Dichlorophenoxy)butyric acid (2,4-DB), (4-Chloro-o-tolyloxy)acetic acid (MCPA), 4-(4-Chloro-o-tolyloxy)butyric acid, 4-(4-Chlorophenoxy)butyric acid, 3,6-Dichloro-2-methoxybenzoic acid (Dicamba), 1-(Ethoxycarbonyl)ethyl-3,6-dichloro-2-methoxybenzyl (lactidichloroethyl). Preferred safeners in combination with the herbicide combinations according to the invention are: cloquintocet-mexyl, cyprosulfamide, fenchlorazole ethyl ester, isoxadifen-ethyl, mefenpyr-diethyl, fenchlorin, cumyluron, S4-1 and S4-5, and particularly preferred safeners are: cloquintocet-mexyl, cyprosulfamide, isoxadifen-ethyl and mefenpyr-diethyl. The herbicide combinations according to the invention may contain other components, e.g. B. Plant growth regulators or other active substances that affect harmful organisms such as harmful plants, plant-harming animals or plant-harming insects, in particular active ingredients from the group of herbicides, fungicides, insecticides, acaricides, nematodes, miticides and related substances. Examples of plant growth regulators that can be used as mixing partners are: acibenzolar, acibenzolar-S-methyl, 5-aminolevulinic acid, ancymidol, 6-benzylaminopurine, brassinolide, catechin, chlormequat chloride, clopp, cocyclonilide.3-(Cycloprop-1-enyl)propionic acid, BCS231024-Ausland STR 64 daminozide, dazomet, n-decanol, dikegulac, dikecg-suoladium, endothal, endothal-dipotassium, -disodium, and mono(N,N-dimethylalkmymlaonium), ethephon, flumetraline, flurenol, flurenol-butyl, flurprimidol, forchlorfenuron, gibebrellic acid, inabenfide, indol-3-acetic acid (IA,A 4)- indol-3-ylbutyric acid, isoprothiolane, probenaz,o Jleasmonic acid, jasmonic acid methyl ester, maleic hydrazide, mepiquat chloride, 1-methylcycloprope 2n-e(1,-naphthyl)acetamide, 1-naphthylacetic acid, 2-naphthyloxyacetic acid, nitrophenolate mixture, 4o-O-4[(2-phenylethyl)amino]butyric acid, paclobutrazol, N-phenylphthalamic acid, prohexaed, pnrohexadione-calcium, prohydrojasmone, salicylic acid, strigolactone, tecnazene, thidiazu trroianc,ontanol, trinexapac, trinexapac-ethyl, tseitfo,d uniconazole, uniconazole-P. Fungicidal compounds which can be used in combination with the herbicide combinations according to the invention,b preferably commercially available active ingredients, for example (analogous to herbicides, compound compounds are generally referred to by their common names, here in the usual English spelling iisbe): 1) Inhibitors of ergosterol biosynthesis, for example (1.001) Cyproconazole, (1.002) Difenoconazole, (1.003) Epoxiconazole, (1.004) Fenhexamid, (1.005) Fropidin, (1.006) Fenpropimorph, (1.007) Fenpyrazamine, (1.008) Fluquinconazole, (1.009) Fialufotril, (1.010) Imazalil, (1.011) Imazalil Sulfate, (1.012) Ipconazole, (1.013) Metconazole, (1,014) Moybcultanil, (1,015) Paclobutrazol, (1,016) Prochlo,raz (1,017) Propiconazole, (1,018) Prothioconazole, (19.)0 Pyrisoxazole, (1,020) Spiroxamine, (1,021) Tebuconazole, (1,022) Tetraconazole, (1.023) Triadnioml,e (1.024) Tridemorph, (1.025) Triticonazole, (1.026) (1R,2S,5S)-5-(4-Chlorobenzyl)-2-(chlorome)th-2y-lmethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.027) (1S,2R,5R)-5-(4-oCrhblenzyl)-2-(chloromethyl)-2-methyl-1-(1H-1,2,4- triazol-1-ylmethyl)cyclopentanol, (1.028) (2R)-2--C(1hlorcyclopropyl)-4-[(1R)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (1.029) (2R)(-12- Chlorcyclopropyl)-4-[(1S)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-1-yl)buta2n--ol, (1.030) (2R)-2-[4-(4-Chlorphenoxy)-2- (trifluormethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)porpan-2-ol, (1.031) (2S)-2-(1-Chlorcyclopropyl)-4- [(1R)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triazol-y1l)butan-2-ol, (1.032) (2S)-2-(1-Chlorcycloprop-yl) 4-[(1S)-2,2-dichlorcyclopropyl]-1-(1H-1,2,4-triaz-o1l-yl)butan-2-ol, (1.033) (2S)-2-[4-(4- Chlorphenoxy)-2-(trifluormethyl)phenyl]-1-(1H-1,2-,t4riazol-1-yl)propan-2-ol, (1.034) (R)-[3-(4-Chlor- 2-fluorphenyl)-5-(2,4-difluorphenyl)-1,2-oxazol-4l]-(ypyridin-3-yl)methanol, (1.035) (S)-[3-(4-Chlor--2 fluorphenyl)-5-(2,4-difluorphenyl)-1,2-oxazol-4-y(pl]yridin-3-yl)methanol, (1.036) [3-(4-Chlor-2- fluorphenyl)-5-(2,4-difluorphenyl)-1,2-oxazol-4-y(pl]yridin-3-yl)methanol, (1.037) 1-({(2R,4S)-2-[2- Chlor-4-(4-chlorphenoxy)phenyl]-4-methyl-1,3-dioxaonl-2-yl}methyl)-1H-1,2,4-triazol, (1.038) 1- ({(2S,4S)-2-[2-Chlor-4-(4-chlorphenoxy)phenyl]-4-mtheyl-1,3-dioxolan-2-yl}methyl)-1H-1,2,4-triazol, (1.039) 1-{[3-(2-Chlorphenyl)-2-(2,4-difluorphenyolx)iran-2-yl]methyl}-1H-1,2,4-triazol-5-yl- thiocyanat, (1.040) 1-{[rel(2R,3R)-3-(2-Chlorphe)n-y2l-(2,4-difluorphenyl)oxiran-2-yl]methyl}-1H- 1,2,4-triazol-5-yl-thiocyanat, (1.041) 1-{[rel(2RS,3)-3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2- BCS231024-Ausland STR 65 yl]methyl}-1H-1,2,4-triazol-5-yl-thiocyanat, (1.04)2 -[(2R,4R,5R)-1-(2,4-Dichlorphenyl)-5-hydroxy- 2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4ia-tzrol-3-thion, (1.043) 2-[(2R,4R,5S)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4]-y 2l,4-dihydro-3H-1,2,4-triazol-3-thion, (1.044) 2-[(2R,4S,5R)-1-(2,4-Dichlorophenyl)-5-hydroxy-2,6t,r6im- ethylheptan-4-yl]-2,4-dihydro-3H-1,2,4- triazol-3-thion, (1.045) 2-[(2R,4S,5S)-1-(2,4-Diochrplhenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2-,4dihydro-3H-1,2,4-triazol-3-thion, (1.046) 2-[(2S,,45R )-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triaz3o-l-thion, (1.047) 2-[(2S,4R,5S)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4]-y 2l,4-dihydro-3H-1,2,4-triazol-3-thion, (1.048) 2-[(2S,4S,5R)-1-(2,4-Dichlorphenyl)-5-hydroxy-2,6,r6im-tethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol- 3-thion, (1.049) 2-[(2S,4S,5S)-1-(2,4-Dichlorphe)n-5y-lhydroxy-2,6,6-trimethylheptan-4-yl]-2,4- dihydro-3H-1,2,4-triazol-3-thion, (1.050) 2-[1-(2-D,4ichlorphenyl)-5-hydroxy-2,6,6-trimethylheptan-4-yl]-2,4-dihydro-3H-1,2,4-triazol-3-thion, (1.051)-[ 2 -Chlor-4-(2,4-dichlorophenoxy)phenyl]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.052) 2-[2-Chl4or-(-4-chlorphenoxy)phenyl]-1-(1H-1,2,4-triazol-1- yl)butan-2-ol, (1.053) 2-[4-(4-Chlorphenoxy)-2-f(lturiormethyl)phenyl]-1-(1H-1,2,4-triazol-1-yl)butan- 2-ol, (1.054) 2-[4-(4-Chlorphenoxy)-2-(trifluormeytlh)phenyl]-1-(1H-1,2,4-triazol-1-yl)pentan-2-ol, (1.055) 2-[4-(4-Chlorphenoxy)-2-(trifluormethyl)pnhyel]-1-(1H-1,2,4-triazol-1-yl)propan-2-ol, (1.056) 2-{[3-(2-Chlorphenyl)-2-(2,4-difluorphenyl)oxiran-y2l]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-thion, (1.057) 2-{[rel(2R,3R)-3-(2-Chlorphenyl)-2-(2,4-dluiforphenyl)oxiran-2-yl]methyl}-2,4-dihydro-3H- 1,2,4-triazol-3-thion, (1.058) 2-{[rel(2R,3S)-3-(C2h-lorphenyl)-2-(2,4-difluorphenyl)oxiran-2- yl]methyl}-2,4-dihydro-3H-1,2,4-triazol-3-thion, (.0159) 5-(4-Chlorbenzyl)-2-(chlormethyl)-2-methyl- 1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol, (1.00)65-(Allylsulfanyl)-1-{[3-(2-chlorphenyl)-2-(2,4- difluorphenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazo (l,1.061) 5-(Allylsulfanyl)-1-{[rel(2R,3R)-3-(2- chlorphenyl)-2-(2,4-difluorphenyl)oxiran-2-yl]metlh}-y1H-1,2,4-triazol, (1.062) 5-(Allylsulfanyl)-1- {[rel(2R,3S)-3-(2-chlorphenyl)-2-(2,4-difluorphen)yolxiran-2-yl]methyl}-1H-1,2,4-triazol, (1.063) N'- (2,5-Dimethyl-4-{[3-(1,1,2,2-tetrafluorethoxy)pheln]syulfanyl}phenyl)-N-ethyl-N- methylimidoformamid, (1.064) N'-(2,5-Dimethyl-4-{-[(32,2,2-trifluorethoxy)phenyl]sulfanyl}phenyl)- N-ethyl-N-methylimidoformamid, (1.065) N'-(2,5-Dimtheyl-4-{[3-(2,2,3,3- tetrafluorpropoxy)phenyl]sulfanyl}phenyl)-N-ethyl-Nmethylimidoformamid, (1.066) N'-(2,5-Dimethyl- 4-{[3-(pentafluorethoxy)phenyl]sulfanyl}phenyl)-Nt-heyl-N-methylimidoformamid, (1.067) N'-(2,5- Dimethyl-4-{3-[(1,1,2,2-tetrafluorethyl)sulfanyl]pehnoxy}phenyl)-N-ethyl-N-methylimidoformamid, (1.068) N'-(2,5-Dimethyl-4-{3-[(2,2,2-trifluoreth)yslulfanyl]phenoxy}phenyl)-N-ethyl-N- methylimidoformamid, (1.069) N'-(2,5-Dimethyl-4-{[3(2-,2,3,3- tetrafluorpropyl)sulfanyl]phenoxy}phenyl)-N-ethyl-Nmethylimidoformamid, (1.070) N'-(2,5-Dimethyl- 4-{3-[(pentafluorethyl)sulfanyl]phenoxy}phenyl)-Nt-heyl-N-methylimidoformamid, (1.071) N'-(2,5-Dimethyl-4-phenoxyphenyl)-N-ethyl-N-methylimidoforam id, (1.072) N'-(4-{[3-(Difluormethoxy)phenyl]sulfanyl}-2,5-dimethylphen)y-Nl -ethyl-N-methylimidoformamid, (1.073) N'- (4-{3-[(Difluormethyl)sulfanyl]phenoxy}-2,5-dimethlyphenyl)-N-ethyl-N-methylimidoformamid, BCS231024-Ausland STR 66 (1.074) N'-[5-Brom-6-(2,3-dihydro-1H-inden-2-ylox-y2)-methylpyridin-3-yl]-N-ethyl-N- methylimidoformamid, (1.075) N'-{4-[(4,5-Dichlor-31-,thiazol-2-yl)oxy]-2,5-dimethylphenyl}-N-ethyl- N-methylimidoformamid, (1.076) N'-{5-Brom-6-[(1R)-(13,5-difluorophenyl)ethoxy]-2-methylpyridin- 3-yl}-N-ethyl-N-methylimidoformamid, (1.077) N'-{5B-rom-6-[(1S)-1-(3,5-difluorphenyl)ethoxy]-2- methylpyridin-3-yl}-N-ethyl-N-methylimidoformamid (,1.078) N'-{5-Brom-6-[(cis-4- isopropylcyclohexyl)oxy]-2-methylpyridin-3-yl}-N-ehtyl-N-methylimidoformamid, (1.079) N'-{5- Brom-6-[(trans-4-isopropylcyclohexyl)oxy]-2-methylrpidin-3-yl}-N-ethyl-N-methylimidoformamid, (1.080) N'-{5-Bromo-6-[1-(3,5-difluorphenyl)ethox-y2]-methylpyridin-3-yl}-N-ethyl-N- methylimidoformamid, (1.081) Mefentrifluconazole1,.0 (82) Ifentrifluconazole. 2) Respiratory chain inhibitors at Complex I or other examples (2.001) Benzovindiflupyr, (2.002) Bixafen, (2.003) Boscalid, (2.004) Carboxin, (2.000 F5luopyram, (2.006) Flutolanil, (2.007) Fluxapyroxad, (2.008) Furametpyr, (2.009) Isofetda,m (2i.010) Isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (2.011) Isopyrazam (anti-epimeric enantiomer 1S,4R,9R), (2.012) Isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (2.013) Isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), 1RS,4SR,9RS and the anti-epimeric racemate 1R,S9S,4RS)R, (2.014) Isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (2.015) Isopyrazam (syn-epimeric enantiomer 1S,4R,9S), (2.016) Isopyrazam (syn-epimeric racemate 1RS,4SR,9RS), (2.017) Penf,lu (2f.018) Penthiopyrad, (2.019) Pydiflumetofen, (2.020) Pyraziflumid, (2.021) Seadnaex, (2.022) 1,3-Dimethyl-N-(1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl)-1H-pyrazole-4-carboxamide, (2.3) 1,3-Dimethyl-N-[(3R)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid,0 (2.4) 1,3-Dimethyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyrazol-4-carboxamid,0 (2.5) 1-Methyl-3-(trifluormethyl)-N-[2'-(trifluormethyl)biphenyl-2-yl]-1H-pyrazol-4-carboxmaid, (2.026) 2-Fluor-6-(trifluoromethyl)-N-(1,1,3- trimethyl-2,3-dihydro-1H-inden-4-yl)benzamid, (2.70)23-(Difluormethyl)-1-methyl-N-(1,1,3-trimethyl- 2,3-dihydro-1H-inden-4-yl)-1H-pyrazol-4-carboxam (id2,.028) 3-(Difluormethyl)-1-methyl-N-[(3R)- 1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1H-pyroalz-4-carboxamid, (2.029) 3-(Difluormethyl)-1- methyl-N-[(3S)-1,1,3-trimethyl-2,3-dihydro-1H-ind-e4n-yl]-1H-pyrazol-4-carboxamid, (2.030) 3- (Difluormethyl)-N-(7-fluor-1,1,3-trimethyl-2,3-dihdyro-1H-inden-4-yl)-1-methyl-1H-pyrazol-4- carboxamid, (2.031) 3-(Difluormethyl)-N-[(3R)-7-folur-1,1,3-trimethyl-2,3-dihydro-1H-inden-4-yl]-1- methyl-1H-pyrazol-4-carboxamid, (2.032) 3-(Difluomroethyl)-N-[(3S)-7-fluor-1,1,3-trimethyl-2,3- dihydro-1H-inden-4-yl]-1-methyl-1H-pyrazol-4-carbaomxid, (2.033) 5,8-Difluor-N-[2-(2-fluor-4-{[4- (trifluormethyl)pyridin-2-yl]oxy}phenyl)ethyl]quinazolin-4-amin, (2.034) N-(2-Cyclopentyl-5- fluorbenzyl)-N-cyclopropyl-3-(difluormethyl)-5-fluro-1-methyl-1H-pyrazol-4-carboxamid, (2.035) N- (2-tert-Butyl-5-methylbenzyl)-N-cyclopropyl-3-(duiflormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, (2.036) N-(2-tert-Butylbenzyl)-N-cycrlop yl-3-(difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, (2.037) N-(5-Chlor-2-ethylbzeyln)-N-cyclopropyl-3-(difluormethyl)-5-fluor-1- methyl-1H-pyrazol-4-carboxamid, (2.038) N-(5-Ch2lo-ris-opropylbenzyl)-N-cyclopropyl-3- BCS231024-Ausland STR 67 (difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carbxaomid, (2.039) N-[(1R,4S)-9-(Dichlormethylen)- 1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl]-i3fl-u(odrmethyl)-1-methyl-1H-pyrazol-4-carboxamid, (2.040) N-[(1S,4R)-9-(Dichlormethylen)-1,2,3,4-taehtrydro-1,4-methanonaphthalen-5-yl]-3- (difluormethyl)-1-methyl-1H-pyrazol-4-carboxamid2,.0 (41) N-[1-(2,4-Dichlorphenyl)-1- methoxypropan-2-yl]-3-(difluormethyl)-1-methyl-1Hy-rpazol-4-carboxamid, (2.042) N-[2-Chlor-6- (trifluormethyl)benzyl]-N-cyclopropyl-3-(difluormehtyl)-5-fluor-1-methyl-1H-pyrazol-4-carboxamid, (2.043) N-[3-Chlor-2-fluor-6-(trifluormethyl)benz]y-Nl -cyclopropyl-3-(difluormethyl)-5-fluor-1- methyl-1H-pyrazol-4-carboxamid, (2.044) N-[5-Chl2o-r(-trifluormethyl)benzyl]-N-cyclopropyl-3- (difluormethyl)-5-fluor-1-methyl-1H-pyrazol-4-carbxaomid, (2.045) N-Cyclopropyl-3-(difluormethyl)- 5-fluor-1-methyl-N-[5-methyl-2-(trifluormethyl)benyzl]-1H-pyrazol-4-carboxamid, (2.046) N- Cyclopropyl-3-(difluormethyl)-5-fluor-N-(2-fluor-6is-opropylbenzyl)-1-methyl-1H-pyrazol-4- carboxamid, (2.047) N-Cyclopropyl-3-(difluormeth-y5l-)fluor-N-(2-isopropyl-5-methylbenzyl)-1- methyl-1H-pyrazol-4-carboxamid,(2.048) N-Cyclopyrol-p3-(difluormethyl)-5-fluor-N-(2- isopropylbenzyl)-1-methyl-1H-pyrazol-4-carbothioadm, (i2.049) N-Cyclopropyl-3-(difluoromethyl)-5- fluor-N-(2-isopropylbenzyl)-1-methyl-1H-pyrazol-4a-rcboxamid, (2.050) N-Cyclopropyl-3- (difluormethyl)-5-fluor-N-(5-fluor-2-isopropylbenzl)y-1-methyl-1H-pyrazol-4-carboxamid, (2.051) N- Cyclopropyl-3-(difluormethyl)-N-(2-ethyl-4,5-dimeythlbenzyl)-5-fluor-1-methyl-1H-pyrazol-4- carboxamid, (2.052) N-Cyclopropyl-3-(difluormeth-yNl)-(2-ethyl-5-fluorbenzyl)-5-fluor-1-methyl-1H- pyrazol-4-carboxamid, (2.053) N-Cyclopropyl-3-(duioflrmethyl)-N-(2-ethyl-5-methylbenzyl)-5-fluor-1- methyl-1H-pyrazole-4-carboxamid, (2.054) N-Cycloppyrlo-N-(2-cyclopropyl-5-fluorbenzyl)-3- (difluormethyl)-5-fluor-1-methyl-1H-pyrazole-4-caorxbamid, (2.055) N-Cyclopropyl-N-(2-cyclopropyl- 5-methylbenzyl)-3-(difluormethyl)-5-fluor-1-methy1lH- -pyrazole-4-carboxamid,(2.056) N- Cyclopropyl-N-(2-cyclopropylbenzyl)-3-(difluormethl)y-5-fluor-1-methyl-1H-pyrazole-4-carboxamid. 3) Inhibitoren der Atmungskette am Komplex III,s bpeiielsweise (3.001) Ametoctradin, (3.002) Amisulbrom, (3.003) Azoxystrobin, (3.004) Coumetyhsotxrobin, (3.005) Coumoxystrobin, (3.006) Cyazofamid, (3.007) Dimoxystrobin, (3.008) Enoxoabsitnr, (3.009) Famoxadon, (3.010) Fenamidon, (3.011) Flufenoxystrobin, (3.012) Fluoxastrobin.,0 (133) Kresoxim-Methyl, (3.014) Metominostrobin, (3.015) Orysastrobin, (3.016) Picoxystrobin, (3.)0 P17yraclostrobin, (3.018) Pyrametostrobin, (3.019) Pyraoxystrobin, (3.020) Trifloxystrobin (3.021) ()2-2E-{2-[({[(1E)-1-(3-{[(E)-1-Fluor-2- phenylvinyl]oxy}phenyl)ethyliden]amino}oxy)methyl]hpenyl}-2-(methoxyimino)-N-methylacetamid, (3.022) (2E,3Z)-5-{[1-(4-Chlorphenyl)-1H-pyrazol-y3l]-oxy}-2-(methoxyimino)-N,3-dimethylpent-3- enamid, (3.023) (2R)-2-{2-[(2,5-Dimethylphenoxy)mhyelt]phenyl}-2-methoxy-N-methylacetamid, (3.024) (2S)-2-{2-[(2,5-Dimethylphenoxy)methyl]phyel}n-2-methoxy-N-methylacetamid, (3.025) (3S,6S,7R,8R)-8-Benzyl-3-[({3-[(isobutyryloxy)metxhyo]-4-methoxypyridin-2-yl}carbonyl)amino]-6- methyl-4,9-dioxo-1,5-dioxonan-7-yl-2-methylpropant,o (a3.026) 2-{2-[(2,5- Dimethylphenoxy)methyl]phenyl}-2-methoxy-N-methyelatcamid, (3.027) N-(3-Ethyl-3,5,5- BCS231024-Ausland STR 68 trimethylcyclohexyl)-3-formamido-2-hydroxybenzam (id3,.028) (2E,3Z)-5-{[1-(4-Chlor-2-fluorphenyl)- 1H-pyrazol-3-yl]oxy}-2-(methoxyimino)-N,3-dimethyelpnt-3-enamid, (3.029) Methyl {5-[3-(2,4- dimethylphenyl)-1H-pyrazol-1-yl]-2-methylbenzyl}cbaarmate. 4) Inhibitoren der Mitose und Zellteilung, beispsiweleise (4.001) Carbendazim, (4.002) Diethofencarb, (4.003) Ethaboxam, (4.004) Fluopicolid, (4.005)c Pyecnuron, (4.006) Thiabendazol, (4.007) Thiophanat-Methyl, (4.008) Zoxamid, , (4.009) 3-oCrh-4l-(2,6-difluorphenyl)-6-methyl-5- phenylpyridazin, (4.010) 3-Chlor-5-(4-chlorphen4yl-)(-2,6-difluorphenyl)-6-methylpyridazin,(4.011) 3- Chlor-5-(6-chlorpyridin-3-yl)-6-methyl-4-(2,4,6-tflruiorphenyl)pyridazin, (4.012) 4-(2-Brom-4- fluorphenyl)-N-(2,6-difluorphenyl)-1,3-dimethyl-1Hpy-razol-5-amin, (4.013) 4-(2-Brom-4- fluorphenyl)-N-(2-brom-6-fluorphenyl)-1,3-dimethy1lH--pyrazol-5-amin, (4.014) 4-(2-Brom-4- fluorphenyl)-N-(2-bromphenyl)-1,3-dimethyl-1H-pyroalz-5-amin, (4.015) 4-(2-Brom-4-fluorphenyl)-N- (2-chlor-6-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5m-ain, (4.016) 4-(2-Brom-4-fluorphenyl)-N-(2- chlorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, (4.0)147-(2-Brom-4-fluorphenyl)-N-(2-fluorphenyl)- 1,3-dimethyl-1H-pyrazol-5-amin, (4.018) 4-(2-Chl4o-rf-luorphenyl)-N-(2,6-difluorphenyl)-1,3- dimethyl-1H-pyrazol-5-amin, (4.019) 4-(2-Chlor-4u-oflrphenyl)-N-(2-chlor-6-fluorphenyl)-1,3- dimethyl-1H-pyrazol-5-amin, (4.020) 4-(2-Chlor-4u-oflrphenyl)-N-(2-chlorphenyl)-1,3-dimethyl-1H- pyrazol-5-amin, (4.021) 4-(2-Chlor-4-fluorphenyl)--(N2-fluorphenyl)-1,3-dimethyl-1H-pyrazol-5-amin, (4.022) 4-(4-Chlorphenyl)-5-(2,6-difluorophenyl)-3-d,6-dimethylpyridazine, (4.023) N-(2-bromo-6-fluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.024) N-(2-bromophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine, (4.025) N-(4-chloro-2,6-difluorophenyl)-4-(2-chloro-4-fluorophenyl)-1,3-dimethyl-1H-pyrazol-5-amine 5) Compounds capable of multisite activity, for example (5.001) Bordeaux mixture, (5.002) Captafol, (5.003) Captan, (5.004) Chlorothnail,l (5.005) Copper hydroxide, (5.006) Copper naphthenate, (5.007) Copper oxide, (5.008) Curpofxey chloride, (5.009) Copper(2+) sulfate, (5.010) Dithianon, (5.011) Dodine, (5.012) Folpet, (5.013a)n Mcozeb, (5.014) Maneb, (5.015) Metiram, (5.016) Zinc metiram, (5.017) Copper oxine, (5.018) Propyne (5b.,019) Sulfur and sulfur preparations including calcium polysulfide, (5.020) Thiram5,.0 (21) Zineb, (5.022) Ziram, (5.023) 6-Ethyl-5,7- dioxo-6,7-dihydro-5H-pyrrolo[3',4':5,6][1,4]dithioin[2,3-c][1,2]thiazole-3-carbonitrile. 6) connections,which are capable of inducing host defense, for example (6.001) acibenzolar-S-methyl, (6.002) isotianil, (6.003) pyrenazole, (6.004) tiadinil. 7) Inhibitors of amino acid and / or protein synthesis, for example (7.001) cyprodinil, (7.002) kasugamycin, (7.003) kasugamycin hydrochloride, (7.004) oxytetracycline (7.005) pyrimethanil, (7.006) 3-(5-fluoro-3,3,4,4-tetramethyl-t3h,γ4-dihydroisoquinolin-1-yl)quinoline. (8) Inhibitors of ATP production, for example (6.001) silthiofam. BCS231024-Ausland STR 69 9) Inhibitors of cell wall synthesis, for example (9is.0e01) Benthiavalicarb, (9.002) Dimethomorph, (9.003) Flumorph, (9.004) Iprovalicarb, (9.005) Mdaipnropamid, (9.006) Pyrimorph, (9.007) Valifenalate, (9.008) (2E)-3-(4-tert.-Butylphenyl)--(32-chloropyridin-4-yl)-1-(morpholin-4-yl)prop-2-en-1-one, (9.009) (2Z)-3-(4-tert.-Butylphenyl)-3-(2-hydroxyphenyl)-1-(morpholin-4-yl)prop-2-en-1-one.10) Inhibitors of lipid and membrane synthesis,for example (10.001) Propamocarb, (10.002) Propamocarb hydrochloride, (10.003) Tolclofos-Methyl. 11) Inhibitors of melanin biosynthesis, for example (11.001) Tricyclazole, (11.002) 2,2,2-Trifluoroethyl-{3-methyl-1-[(4-methylbenzoyl)amino]butan-2-yl}carbamate. 12) Inhibitors of nucleic acid synthesis, for example (12.001) Benalaxyl, (12.002) Benalaxyl-M(Kiralaxyl), (12.003) Metalaxyl, (12.004) Metalaxyl-Myl (Mefenoxam). 13) Inhibitors of signal transduction, for example (13.001) fludioxonil, (13.002) iprodione, (13.003) procymidone, (13.004) proquinazid, (13.005) quinoaxiamide, (13.006) vinclozolin. 14) Compounds that can act as uncouplers, for example (14.001) fluazinam, (14.002) meptyldinocap. 15) Other compounds, for example (15.00b1s)c Asinic acid, (15.002) Benthiazole, (15.003) Bethoxazine, (15.004) Capsimycin, (15.005) Carvo1n5, (15.006) Quinomethionate, (15.007) Cufraneb, (15.008) Cyflufenamid, (15.009) Cymoxanil, (15.00)1 C0yprosulfamide, (15.011) Flutianil,(15.012) Fosetyl-Aluminium, (15.013) Fosetyl-Calcium, (154.0)1 Fosetyl-Natrium, (15.015) Methylisothiocyanat, (15.016) Metrafenon, (15.01 M7il)diomycin, (15.018) Natamycin, (15.019) Nickel-Dimethyldithiocarbamat, (15.020) Nitrothaslo-Ipropyl, (15.021) Oxamocarb, (15.022) Oxathiapiprolin, (15.023) Oxyfenthiin, (15.024) Ptaecnhlorphenol und Salze, (15.025) Phosphonsäure und deren Salze, (15.026) Propamocarb-fosetyl5a.t0,2 (17) Pyriofenone (Chlazafenone) (15.028) Tebufloquin, (15.029) Tecloftalam, (15.030) Tolniifdae, (15.031) 1-(4-{4-[(5R)-5-(2,6-Difluorphenyl)- 4,5-dihydro-1,2-oxazol-3-yl]-1,3-thiazol-2-yl}pipiedrin-1-yl)-2-[5-methyl-3-(trifluormethyl)-1H- pyrazol-1-yl]ethanon, (15.032) 1-(4-{4-[(5S)-5-(2-D,6ifluorphenyl)-4,5-dihydro-1,2-oxazol-3-yl]-1,3- thiazol-2-yl}piperidin-1-yl)-2-[5-methyl-3-(trifluormethyl)-1H-pyrazol-1-yl]ethanon, (15.033) 2-(6- Benzylpyridin-2-yl)quinazolin, (15.034) 2,6-Dimetlh-1yH,5H-[1,4]dithiino[2,3-c:5,6-c']dipyrrol- 1,3,5,7(2H,6H)-tetron, (15.035) 2-[3,5-Bis(difluoermthyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-(prop-2-in-1- yloxy)phenyl]-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thziaol-2-yl)piperidin-1-yl]ethanon, (15.036) 2-[3,5- Bis(difluormethyl)-1H-pyrazol-1-yl]-1-[4-(4-{5-[2-hclor-6-(prop-2-in-1-yloxy)phenyl]-4,5-dihydro-1,2- oxazol-3-yl}-1,3-thiazol-2-yl)piperidin-1-yl]ethanno, (15.037) 2-[3,5-Bis(difluormethyl)-1H-pyrazol-1- yl]-1-[4-(4-{5-[2-fluor-6-(prop-2-in-1-yloxy)pheny]l-4,5-dihydro-1,2-oxazol-3-yl}-1,3-thiazol-2- yl)piperidin-1-yl]ethanon, (15.038) 2-[6-(3-Fluor--m4ethoxyphenyl)-5-methylpyridin-2-yl]quinazolin, BCS231024-Ausland STR 70 (15.039) 2-{(5R)-3-[2-(1-{[3,5-Bis(difluormethyl)-H1-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4 yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorphenyl meathnesulfonat, (15.040) 2-{(5S)-3-[2-(1-{[3,5- Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidi-n4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5- yl}-3-chlorphenyl methanesulfonat, (15.041) 2-{27-,[8(-Difluor-2-methylquinolin-3-yl)oxy]-6- fluorphenyl}propan-2-ol, (15.042) 2-{2-Fluor-6-[(f8lu-or-2-methylquinolin-3-yl)oxy]phenyl}propan-2- ol, (15.043) 2-{3-[2-(1-{[3,5-Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidin-4-yl)-1,3-thiazol-4- yl]-4,5-dihydro-1,2-oxazol-5-yl}-3-chlorphenyl-meathnsulfonat, (15.044) 2-{3-[2-(1-{[3,5- Bis(difluormethyl)-1H-pyrazol-1-yl]acetyl}piperidi-n4-yl)-1,3-thiazol-4-yl]-4,5-dihydro-1,2-oxazol-5-yl}phenyl methanesulfonat, (15.045) 2-Phenylphe unnodl deren Salze, (15.046) 3-(4,4,5-Trifluor-3,3-dimethyl-3,4-dihydroisoquinolin-1-yl)quinolin, (1054.7) 3-(4,4-Difluor-3,3-dimethyl-3,4- dihydroisoquinolin-1-yl)quinolin, (15.048) 4-Amin5o--fluorpyrimidin-2-ol (Tautomere Form: 4-Amino- 5-fluorpyrimidin-2(1H)-on), (15.049) 4-Oxo-4-[(2-pehnylethyl)amino]buttersäure, (15.050) 5-Amino- 1,3,4-thiadiazol-2-thiol, (15.051) 5-Chlor-N'-phel-nNy'-(prop-2-yn-1-yl)thiophen-2-sulfonohydrazid, (15.052) 5-Fluor-2-[(4-fluorbenzyl)oxy]pyrimidin-4am- in,(15.053) 5-Fluor-2-[(4- methylbenzyl)oxy]pyrimidin-4-amin, (15.054) 9-Flu-2o,r2-dimethyl-5-(quinolin-3-yl)-2,3-dihydro-1,4- benzoxazepin, (15.055) But-3-yn-1-yl {6-[({[(Z)-(m1-ethyl-1H-tetrazol-5- yl)(phenyl)methylen]amino}oxy)methyl]pyridin-2-yl}acrbamat, (15.056) Ethyl (2Z)-3-amino-2-cyano- 3-phenylacrylat, (15.057) Phenazin-1-carbonsäu1r5e.,0 (58) Propyl 3,4,5-trihydroxybenzoat, (15.059) Quinolin-8-ol, (15.060) Quinolin-8-ol sulfat (2:1 ()1,5.061) tert-Butyl {6-[({[(1-methyl-1H-tetrazol-5 yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-ycl}arbamat, (15.062) 5-Fluor-4-imino-3-methyl- 1)sulfonyl]-3,4-dihydropyrimidin-2(1H)-one. Bevorzugte Fungizide sind ausgewählt aus der Gru bpepsteehend aus Benalaxyl, Bitertanol, Bromuconazol, Captafol, Carbendazim, Carpropamyida,z Cofamid, Cyproconazol, Diethofencarb,Edifenphos, Fenpropimorph, Fentine, Fluquincona Fzo sl,etyl, Fluoroimide, Folpet, Iminoctadine,Iprodionem, Iprovalicarb, Kasugamycin, Maneb, Nab,a Pmencycuron, Prochloraz, Propamocarb,Propineb, Pyrimethanil, Sprioxamine, Quintozeneb, and Tceonazole, Tolylfluanid, Triadimefon, Triadimenol, Trifloxystrobin, Zineb. Insecticidal, acaricidal, nematicidal, miticidal and related active ingredients are, for example (analogous to herbicides and fungicides, the compounds are referred to by their common names where possible, here in the usual English spelling): (1) Acetylcholinesterase (AChE) inhibitors, preferably carbamates selected from alanylcarb, aldicarb, bendiocarb, benfuracarb, butocarboxim, butycarboxim, carbaryl, carbofuran, carbosulfan, ethiofencarb, fenobucarb, formetan, fenofiber, thiocarb, isoprocarb, methiocarb, methomyl, metolcarb, oxamyl, pirimicarb, propoxur, thiodic, triazamate, trimethacarb, XMC and xylylcarb, or organophosphates selected from acetylcarb, p Azamethiphos, Azinphos-ethyl, Azinphos-BCS231024-Ausland STR 71 methyl, Cadusafos, Chlorethoxyfos, Chlorfenvinph Cohsl,ormephos, Chlorpyrifos-methyl, Coumaphos, Cyanophos,Demeton-S-methyl, Diazinon, DichlorvoDsV / DP, Dicrotophos, Dimethoate, Dimethylvinphos, Disulfoton, EPN, Ethion, Ethopropsh, Famphur, Fenamiphos, Fenitrothion, Fenthion, Fosthiazate, Heptenophos, Imicyafos, Inspohfeos, Isopropyl-O-(methoxyaminothio- phosphoryl)salicylate, Isoxathion, Malathion, Mecamrb, Methamidophos, Methidathion, Mevinphos, Monocrotophos, Naled, Omethoate, Oxydemeton-me Pthayrla,thion-methyl, Phenthoate, Phorate, Phosalon, Phosmet, Phosphamidone, Phoxim, Pirim-ipmheotshyl, Profenofos, Propetamphos, Prothiofos, Pyraclofos, Pyridaphenthion, quinalphos, sulfotere, tepimorphoside, temephos, terbufos, tetrachlorvinphos, thiomethyl, triazophos, triclon, and vamidothion. (2) GABA-gated chloride channel blockers, preferably cyclodiene organochlorines selected from chlordane and endosulfan, or phenylpyrazoles (fleipr) selected from ethiprol and fipronil. (3) Sodium channel modulators, preferably pyrolysis, selected from acrinathrin, allethrin, d-cis-trans-allethrin,d-trans-allethrin, bifenthrin, baiollethrin, bioallethrin-S-cyclopentenyl isomer, bioresmethrin, cycloprothrin, cyfluthrin, beta-cuytfhlrin, cyhalothrin, lambda-cyhalothrin, gamma-cyhalothrin, cypermethrin, alpha-cypermethrin, b-ceytapermethrin, theta-cypermethrin, zeta-cypermethrin, cyphenothrin [(1R)-trans isomer],t dalethrin, empenthrin [(EZ)-(1R) isomer], esfenvalerate, etofenprox, fenpropathrin, Fenva,le Frlautcythrinat, flumethrin, tau-fluvalinate, halfenprox, imiprothrin, kadethrin, momfluorothrin P,ermethrin, Phenothrin [(1R)-trans-isomer], prallethrin, pyrethrins (pyrethrum), resmethrin, sluofen, tefluthrin, tetramethrin, tetramethrin [(1R)-isomer], tralomethrin and transfluthrin, or DeDrT or methoxychlor. (4) Competitive modulators of the nicotinic acetyolin receptor (nAChR), preferably neonicotinoids selected from acetamiprid, clotidine, dinotefuran, imidacloprid, nitenpyram, thiacloprid and thiamethoxam, or nicotine,or suximines selected from sulfoxaflor, or butenolides selected from flupyradifurone. (5) Allosteric modulators of the nicotinic acylcholine receptor (nAChR), preferably spinosyns selected from spinetoram and spinosad. (6) Allosteric modulators of the glutamate-dependent glucocorticoid channel (GluCl), preferably avermectins / milbemycins selected from abamectin, emectin benzoate, lepimectin and milbemectin. (7) Juvenile hormone mimetics, preferably juvenile hormone analogues selected from hydroprene, kinoprene and methoprene, or fenoxycarb or polypyrimidine. BCS231024-Ausland STR 72 (8) Various non-specific (multi-site)ib initiators, preferably alkyl halides selected from methyl bromide and other alkyl halides,Odhelro Cropicrin or sulfuryl fluoride or borax or tartar emetic or methyl isocyanate generators selected from diazomet and metam. (9) TRPV channel modulators of chordotonal organs selected from pymetrozine and pyrifluquinazone. (10) Mite growth inhibitors selected from cnlotefzin, hexythiazox, diflovidazine, and etoxazole. (11) Microbial disruptors of the insect intestinal membrane selected from Bacillus thuringiensis subspecies israelensis, Bacillus sphaericus, Bacillus thuringiensis subspecies saizawai, Bacillus thuringiensis subspecies kurstaki, Bacillus thuringiensis subspecies tenebrionis and Bt plant proteins selected from Cry1Ab, Cry1Ac, Cry1CFary, Cry1A.105, Cry2Ab, VIP3A, mCry3A, Cry3Ab, Cry3Bb and Cry34Ab1 / 35Ab1. (12) Inhibitors of mitochondrial ATP synthase, preferably ATP disruptors selected from diafenthiuron, or organotin compounds selected from azocyclotin, cyhexatin and fenbutatin oxide.or propargite or tetradifon. (13) Uncouplers of oxidative phosphorylation by disrupting the proton gradient selected from chlorfenapyr, DNOC, and sulfluramide. (14) Blockers of the nicotinic acetylcholine receptor selected from bensultap, cartap hydrochloride, thiocyclam, and thiosultap sodium. (15) Inhibitors of chitin biosynthesis, type 0, selected from bistrifluron, chlorfluazuron, diflubenzuron, flucycloxuron, flufenoxuron, hexamfluron, lufenuron, novaluron, noviflumuron, teflubenzuron, and triflumuron. (16) Chitin biosynthesis type 1 inhibitors selected from buprofen. (17) Moulting disruptor (particularly in Diptera) selected from cyromazine. (18) Ecdysone receptor agonists selected from caffeonozide, halofenozide, methoxyfenozide, and tebufenozide. (19) Octopamine receptor agonists selected from amoxicillin. (20) Mitochondrial complex III electron transport inhibitors selected from hydramethylnon,Acequinocyl and fluacrypyrim. (21) Mitochondrial complex I electron transport inhibitors, preferably METI acaricides selected from fenazaquin, fenpyroximate, pyrimani, pifeyridaben, tebufenpyrad, and tolfenpyrad, or rotenone (Derris). BCS231024-Ausland STR 73 (22) Voltage-dependent sodium channel blockers selected from indoxacarb and metaflumizone. (23) Acetyl-CoA carboxylase inhibitors, preferably tetronic and tetramic acid derivatives selected from spirodiclofen, spiromesifen, and stearisto. (24) Inhibitors of mitochondrial complex IV ectreon transport, preferably phosphines selected from aluminum phosphide, calcium phosphide, and zinc phosphide, or cyanides selected from calcium cyanide, potassium cyanide, and numacrylate cyanide. (25) Inhibitors of mitochondrial complex II ectreon transport, preferably beta-ketonitrile derivatives selected from cyenopyrafen and hydflumetofen, or carboxanilides selected from pyflubumide. (28) Ryanodine receptor modulators,Preferably, diazepams selected from chlorantraniliprole, cyantraniliprole, and flubendiamide. (29) Modulators of chordotonal organs (with undetermined target structure) selected from flonicamide. (30) further active ingredients selected from Acynonap Ayfird,opyropen, Afoxolaner, Azadirachtin, Benclothiaz, Benzoximate, Benzpyrimoxane, Bifenaz Barto,flanilide, Bromopropylate, Quinomethionate, Chloroprallethrin, Cryolit, Cyclaniliprol, Cycloxaripd, Cyhalodiamid, Dicloromezotiaz, Dicofol, epsilon-Metofluthrin, epsilon-Momfluthrin, Flometuoiqn, Fluazaindolizin, Fluensulfone, Flufenerim, Flufenoxystrobin, Flufiprol, Fluhexafon, Fluopyram, Fl,upyrimin, Fluralaner, Fluxametamide, Fufenozide, Guadipyr, Heptafluthrin, Imidaclothiz, Iprodionea, kappa-Bifenthrin, kappa-Tefluthrin, Lotilaner, Meperfluthrin, Oxazosulfyl, Paichongding, Pyrida,l Pylyrifluquinazone, Pyriminostrobin, Spirobudiclofen, Spiropidion, Tetramethylfluthrin Tne,traniliprole, Tetrachlorantraniliprole, Tigolaner, Tioxazafen, Thiofluoximate,Triflumezopyrim and Iodemthane; Furthermore, preparations based on Bacillus firmus (I-1582, BioNeem, Votivo), as well as the following compounds: 1-{2-Fluoro-4-methyl-5-[(2,2,2-trifluoroethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-1H-1,2,4-triazol-5-amine (known from WO2006 / 043635) (CAS 885026-50-6), {1'-[(2E)-3-(4-ioCrhphenyl)prop-2-en-1-yl]-5-fluorospiro[indol-3,4'-piperidin]-1(2H)-yl}(2-chloropyridin-4-yl)methnaone (known from WO2003 / 106457) (CAS 637360-23-7), 2-Chloro-N-[2-{1-[(2E)-3-(4-chlorophenyl)pro2p-en-1-yl]piperidin-4-yl}-4-(trifluoromethyl)phenyl]isonicotinamide (known a WusO2006 / 003494) (CAS 872999-66-1), 3-(4-chloro- 2,6-dimethylphenyl)-4-hydroxy-8-methoxy-1,8-diaziarosp[4.5]dec-3-en-2-one (known from WO 2010052161) (CAS 1225292-17-0), 3-(4-chloro-2, 6-edtihmylphenyl)-8-methoxy-2-oxo-1,8- diazaspiro[4.5]dec-3-en-4-yl-ethyl carbonate (also known as EP 2647626) (CAS-1440516-42-6), 4-(But-2-yn-1-yloxy)-6-(3,5-dimethylpiperidin-1-yl)-5-fluoroprimidine (known from WO2004 / 099160) (CAS 792914-58-0), PF1364 (known from JP2010 / 01858A6S)- (RCeg.No.1204776-60-2), (3E)-3-[1-[(6-chloro-3-pyridyl)methyl]-2-pyridylidene]-1,1,1-trifluoropropan-2-one (known from WO2013 / 144213) (CAS 1461743-15-6), N-[3-(benzylcarbamoyl)-4-chlorophe]-n1y-lmethyl-3-(pentafluoroethyl)-4- BCS231024-Ausland STR 74 (trifluoromethyl)-1H-pyrazole-5-carboxamide (known from WO2010 / 051926) (CAS 1226889-14-0), 5-bromo-4-chloro-N-[4-chloro-2-methyl-6-(methylcarbamo)pyhlenyl]-2-(3-chloro-2-pyridyl)pyrazole-3-carboxamide (known from CN103232431) (CAS 1449242-30)-,44-[5-(3,5-Dichlorophenyl)-4,5-dihydro- 5-(trifluoromethyl)-3-isoxazolyl]-2-methyl-N-(cis-1o-xido-3-thietanyl)benzamide, 4-[5-(3,5- Dichlorophenyl)-4,5-dihydro-5-(trifluoromethyl)-3-isoazolyl]-2-methyl-N-(trans-1-oxido-3-thietanyl)benzamide and 4-[(5S)-5-(3,5-Dichlorophe)n-4y,l5-dihydro-5-(trifluormethyl)-3-isoxazolyl]-2- methyl-N-(cis-1-oxido-3-thietanyl)benzamid (bekan anuts WO 2013 / 050317 A1) (CAS 1332628-83-7), N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethy-l3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid, (+-) N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethy-l3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid und (-)-N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethyl-3-[(3,3,3-trifluorpropyl)sulfinyl]propanamid (bekannt aus WO 2013 / 162715 A2, WO 2013 / 162716 U AS2, 2014 / 0213448 A1) (CAS 1477923-37-7), 5-[[(2E)-3-Chlor-2-propen-1-yl]amino]-1-[2,6-dichrl-o4-(trifluormethyl)phenyl]-4- [(trifluormethyl)sulfinyl]-1H-pyrazol-3-carbonitreil (bekannt aus CN 101337937 A) (CAS 1105672-77-2), 3-Brom-N-[4-chlor-2-methyl-6-[(methylamino)thxio methyl]phenyl]-1-(3-chlor-2-pyridinyl)-1H-pyrazol-5-carboxamid, (Liudaibenjiaxuanan, beka anunst CN 103109816 A) (CAS 1232543-85-9); N-[4-Chlor-2-[[(1,1-dimethylethyl)amino]carbonyl]-6-emthylphenyl]-1-(3-chlor-2-pyridinyl)-3- (fluormethoxy)-1H-pyrazol-5-carboxamid (bekannt aWuOs 2012 / 034403 A1) (CAS 1268277-22-0), N- [2-(5-Amino-1,3,4-thiadiazol-2-yl)-4-chlor-6-methpyhlenyl]-3-brom-1-(3-chlor-2-pyridinyl)-1H- pyrazol-5-carboxamid (bekannt aus WO 2011 / 08557)5 ( AC1AS 1233882-22-8), 4-[3-[2,6-Dichlor-4- [(3,3-dichlor-2-propen-1-yl)oxy]phenoxy]propoxy]-m2-ethoxy-6-(trifluormethyl)pyrimidin (bekannt aus CN 101337940 A) (CAS 1108184-52-6); (2E)- und 22(Z-[)2--(4-Cyanophenyl)-1-[3- (trifluormethyl)phenyl]ethyliden]-N-[4-(difluormetohxy)phenyl]hydrazincarboxamid (bekannt aus CN 101715774 A) (CAS 1232543-85-9); Cyclopropancarbäounres-3-(2,2-dichlorethenyl)-2,2-dimethyl-4- (1H-benzimidazol-2-yl)phenylester (bekannt aus C0N35124422 A) (CAS 1542271-46-4); (4aS)-7- Chlor-2,5-dihydro-2-[[(methoxycarbonyl)[4-[(trifluromethyl)thio]phenyl]amino]carbonyl]indeno[1,2- e][1,3,4]oxadiazin-4a(3H)-carbonsäuremethylesterka (bnnt aus CN 102391261 A) (CAS 1370358-69- 2); 6-Desoxy-3-O-ethyl-2,4-di-O-methyl-1-[N-[4-[14--[(1,1,2,2,2-pentafluorethoxy)phenyl]-1H-1,2,4- triazol-3-yl]phenyl]carbamatα]--L-mannopyranose (bekannt aus US 2014 / 0275503C AA1)S ( 1181213- 14-8); 8-(2-Cyclopropylmethoxy-4-trifluormethylphoexny)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (CAS 1253850-56-4), (8-a-8n-ti()2-Cyclopropylmethoxy-4- trifluormethylphenoxy)-3-(6-trifluormethylpyridaz-i3n-yl)-3-azabicyclo[3.2.1]octan (CAS 933798-27- 7), (8-syn)-8-(2-Cyclopropylmethoxy-4-trifluormetlhpyhenoxy)-3-(6-trifluormethylpyridazin-3-yl)-3- azabicyclo[3.2.1]octan (bekannt aus WO 2007040218,0 W AO 2007040282 A1) (CAS 934001-66-8), N-[3-Chlor-1-(3-pyridinyl)-1H-pyrazol-4-yl]-N-ethy-l3-[(3,3,3-trifluorpropyl)thio]-propanamid (bekannt aus WO 2015 / 058021 A1,WO 2015 / 058028 (AC1A)S 1477919-27-9) and N-[4-(aminothioxomethyl)-2-methyl-6-[(methylamino)carbyol]nphenyl]-3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide (known from CN 1032655)27 (C AAS 1452877-50-7), 5-(1,3-Dioxan-2-yl)-4-BCS231024-Ausland STR 75 [[4-(trifluoromethyl)phenyl]methoxy]-pyrimidine (known from WO 2013 / 115391 A1) (CAS 1449021-97-9), 3-(4-Chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-1,8-diazaspiro[4.5]decane-2,4-dione (known from WO 2014 / 187846 A1) (CAS 1638765-58-8), 3-(4-Chloro-2,6-dimethylphenyl)-8-methoxy-1-methyl-2-oxo-1,8-diazaspiro[4.5]dec-3-en-4-yl-carboxylic acid ester (known from WO 2010 / 066780 A1, WO2011151146 A1) (CAS 1229023-00-0), 4-[(5S)-5-(3,5C-chloro-4-fluorophenyl)-4,5-dihydro-5- (trifluoromethyl)-3-isoxazolyl]-N-[(4R)-2-ethyl-3-xoo-4-isoxazolidinyl]-2-methyl-benzamide (known from WO 2011 / 067272, WO2013 / 050302) (CAS 13099593-)6.2- Insecticides which can preferably be used together with the Heidrbeinz,are, for example, the following: Acetamiprid, Acrinathrin, Aldicarb, Amitraz, Acinpohs-methyl, Cyfluthrin, Carbaryl, Cypermethrin, Deltamethrin, Endosulfan, Ethoprophos, Fenamip Pheons,thion, Fipronil, Imidacloprid, Methamidophos, Methiocarb, Niclosamide, Oxydememtoent-hyl, Prothiophos, Silafluofen, Thiacloprid, Thiodicarb, Tralomethrin, Triazophos, Trichlorfo Tnr,iflumuron, Terbufos, Fonofos, Phorate, Chlorpyriphos, Carbofuran, Tefluthrin. The active ingredient combinations according to the invention are suitable for controlling a broad spectrum of weeds in non-cultivated land, on paths, railway tracks, industrial areas ("industrial weed control"), or in plantation crops such as temperate, subtropical tropical climates or geographies. Examples of plantation crops are oil palm, nuts (e.g., almonds, hazelnuts, walnuts, macadamia), coconut, berries, oil palm, gum trees, fruits (e.g., orange, lemon, mandarin), bananas, pineapple, cotton, sugar cane, tea, coffee,for coffee and similar crops. They are also suitable for use in fruit growing (e.g., pome fruits such as apples, blueberries, cherries, mangoes, kiwifruit) and viticulture. The products can also be used for pre-sowing (burn-down, no-till, or zero-till methods) or for post-harvest treatment ("tree fallow"). The application possibilities of the active ingredient combination also extend to weed control in tree crops, e.g., young Christmas tree crops or Edible vines, either before or after planting (also with overhead irrigation). The products can also be used to combat unwanted plant growth in economically important crops such as wheat (durum and wheat flour), maize, soybeans, sugar beet, sugar cane, cotton, rice, beans (such as bush beans and horse beans), flax, barley, oats, rye, triticale, potatoes and millet (sorghum).i Wdeland and green / lawn areas and plantation crops. Plantation crops include, among others, pomefruits (apple, pear, quince), ribes-like fruits (blackberry, raspberry), citrus purpurea, nectarines, almonds), nuts (walnut, pecan, hazelnut, cashew, macadamia), mango, cocoa, coffee, wine (table grapes, BCS231024-Ausland STR 76 grapes), palms (such as oil palm, date palm, oats palm), eucalyptus, kaki, persimmon, rubber, pineapple, banana, avocado, lychee, flowering plants (Eucalyptus, Piniaceae, Piceae, Meliaceae, etc.). The herbicidal active ingredient combinations according to the invention in the respective application forms (= herbicidal agents) exhibit synergies with regard to It exhibits herbicidal activity and selectivity, as well as favorable effects on the weed spectrum. It exhibits excellent herbicidal activity against a broad spectrum of economically important macrocotyledonous and dicotyledonous annual weeds. Even difficult-to-control perennial pests,that sprout from rhizomes, rootstocks, or other permanent organs are effectively controlled by dry weeds. The active ingredient combinations can be applied to plants (e.g., harmful plants such as monocotyledonous or dicotyledonous weeds or undesirable cultivated plants), the seed (e.g., grains, seeds, or vegetative propagation organs such as tubers or late-stage shoots with buds), or the area on which the plants grow (e.g., the cultivated area). The substances can be applied pre-sowing (if necessary, by incorporation into the soil), pre-emergence, or post-emergence. The preferred application is in the early post-sowing pre-emergence method or in the post-emergence method of plantation crops against not yet emerged or already emerged pests. The application can also be used in weed management systems with multiple applications (sequence applications,"sequentials") integrated weeds. In detail, some representatives of the deono- and dicotyledonous weed flora are mentioned as examples, which can be controlled by the active ingredient combination according to the invention, without implying a restriction to specific species. On the side of the monocotyledonous weed species, A zegilops, Agropyron, Agrostis, Alopecurus,Apera, Avena, Brachicaria, Bromus, Cynodon, Dacttyelnoium, Digitaria, Echinochloa, Eleocharis, Eleusine, Eragrostis, Eriochloa, Festuca, Fimblrisis,ty Imperata, Ischaemum, Heteranthera, Imperata, Ischaemum, Leptochloa, Lolium, Monochoria, Panicu Pmas,palum, Phalaris, Phleum, Poa, Rottboellia, Sagittaria, Scirpus, Setaria, Sorghum, Sphenocnleda C uyperus species recorded by the annual group. In dicotyledonous weed species, the Wnirgksu spectrum extends to species such as Abutilon, Amaranthus, Ambrosia, Anoda, Anthemis, Aphanese, Aristia, Atriplex, Bellis, Bidens, Capsella, Carduus, Cassia, Centaurea,Chenopodium, Cirsiuomnv,o Clvulus, Datura, Desmodium, Emex, Erodium, Erysimum, Euphorbia, Galeopsis, Galinso Ggaal,ium, Geranium, Hibiscus, Ipomoea, Kochia, Lamium, Lepidium, Lindernia, Matricaria, Mentha,r Mceurialis, Mullugo, Myosotis, Papaver, Pharbitis, BCS231024-Abroad STR 77 Plantago, Polygonum, Portulaca, Ranunculus, Rapsh,a Rnourrippa, Rotala, Rumex, Salsola, Senecio, Sesbania, Sida, Sinapis, Solanum, Sonchus, Spheean,o Sctlellaria, Taraxacum, Thlaspi, Trifolium, Urtica, Veronica, Viola, Xanthium. If the active ingredient combination according to the invention is applied to the soil surface before germination, either the emergence of the weeds is completely prevented or the weeds grow to the cotyledon stage.However, their growth then ceases and they finally die after three to four weeks. When the active ingredients are applied post-emergence to the green parts of the plants, growth stops after treatment, and the pests remain in the growth stage present at the time of application or die completely within a certain period of time, so that weed competition harmful to the crop plants is eliminated very early and sustainably. The herbicidal compositions according to the invention are characterized by a rapid onset and long-lasting herbicidal action. The rain resistance of the active ingredients in the combinations according to the invention is generally favorable. A particular advantage is that the effective dosages of compounds (A) and (B) used in the combinations can be adjusted so low thatthat their soil effectiveness is generally low. This not only makes their use in sensitive crops possible, but also practically avoids groundwater contamination. The combination of active ingredients according to the invention enables a significant reduction in the required application rate of the active ingredients. With the combined use of herbicides (A) and (nBd), application properties are achieved that go beyond what was to be expected for their combination based on the known properties of the individual herbicides. For example, the herbicidal effects on a specific weed species exceed the expected values ​​that can be estimated using standard methods, e.g., according to Colby or other extrapolation methods. A synergistic effect always exists when the effect,Here, the herbicidal effect of the active ingredient combination is greater than the sum of the effects of the individually applied active ingredients. The expected effect for a given combination of two active ingredients can be calculated according to SR Colby ("Calculating Synergistic and Antagonistic Response of a Herbicide Combination", Weeds 15 (1967), 20-22) (see below). BCS231024-Ausland STR 78 The synergistic effects therefore allow, for example, a reduction in the application rates of the individual active ingredients, a higher potency at a lower application rate, the control of previously unidentified species of weeds (gaps), a higher residual effect, an increased long-term effect, an increased speed of action,no extension of the application period and / or a reduction in the number of necessary applications and - as a result for the user - economically and ecologically advantageous weed control systems. Although the combinations according to the invention have a marked herbicidal activity against mono- and dicotyledonous weeds, economically important crop plants are only insignificantly or not at all affected, depending on the structure of the respective active ingredient combinations according to the invention and their application rate. Economically important crops are, for example, dicotyledonous crops of the genera Arach Bies,ta, Brassica, Cucumis, Cucurbita, Helianthus, Daucus, Glycine, Gossypium, Ipomoea, Lactuca, Li,n Luymcopersicon, Nicotiana, Phaseolus, Pisum, Solanum, Vicia, or monocotyledonous crops of the genera Allium, Ananas, Asparagus, Avena, Hordeum, Oryza, Panicum, Saccharum, Secale, Sor,g Thruitmicale,Triticum and Zea. Furthermore, the compounds according to the invention exhibit outstanding growth-regulating properties in crop plants. They regulate the plant's own metabolism and can thus be used to specifically influence plant components and to facilitate harvesting, for example by inducing desiccation and growth suppression. Furthermore, they are also suitable for the general control and inhibition of undesired vegetative growth without killing the plants. Inhibition of vegetative growth plays a major role in many monocotyledonous and dicotyledonous crops, as lodging can be reduced or completely prevented. Due to their herbicidal and plant growth-regulating properties, the agents can be used to control weeds in known plant varieties or in those yet to be developed, modified or genetically modified by conventional mutagenesis.tolerant crops. The transgenic plants are generally characterized by particularly advantageous properties, in addition to resistance to the inventive agents, for example, resistance to plant pathogens and the cause of plant diseases such as certain insects or microorganisms such as fungi, bacteria or viruses. Other special properties affect, for example, the harvested product in terms of quality, storability, composition, and special ingredients. Strain-genic plants with increased starch content or altered starch quality or those with an altered fatty acid composition of the harvested product are known. Other special properties could include tolerance or resistance to abiotic stressors, e.g. heat, cold, drought,Salt and intraviolet radiation. BCS231024-Ausland STR 79 The active ingredient combinations according to the invention can preferably be used as herbicides in crops which are resistant to the phytotoxic effects of the herbicides or which have been genetically engineered to be resistant. Conventional methods for producing new plants which have modified properties compared to previously occurring plants, for example, in classical breeding methods and the production of mutants, can be used. New plants with modified properties can be created natively using genetic engineering methods (see, for example, EP-A-0221044, EP-A-0131624). For example, several cases have been described: - genetic modifications of crop plants, modification of the starch synthesized in the plants (e.g. WO 92 / 11376, WO 9822 / 174, WO 91 / 19806), - transgenic crop plants which exhibit resistance to other herbicides,for example against sulfonylureas (EP-A-029537, US-A-5013659), - transgenic crops with the ability to produce Bacillus thuringiensis toxins (Bt toxins), which make the plants resistant to certain pests (EP-A-0142924, EP-A-0193259). - transgenic crops with modified moisture composition (WO 91 / 13972). - genetically modified crops with new amino acids or secondary substances, e.g. new phytoalexins, which cause increased disease resistance (EPA 309862, EPA0464461) - genetically modified plants with reduced orospiration, which exhibit higher yields and greater stress tolerance (EPA 0305398). - Transgenic crop plants that produce pharmaceutically important proteins (“molecular pharming”) - transgenic crop plants,which are characterized by higher reactivity or better quality - transgenic crop plants which are characterized by a combination of, for example, the above-mentioned new properties ("gene stacking"). Numerous molecular biological techniques with which new transgenic plants with modified properties can be produced are known in Pipr; see, for example, B. I. Potrykus and G. Spangenberg (eds.) Gene Transfer to Plants, Springer Linagbe Manual (1995), Springer Verlag Berlin, Heidelberg or Christou, "Trends in Plant Science" 1c (e1996) 423-431). BCS231024-Ausland STR 80 For such genetic manipulations, nic acid molecules can be introduced into plasmids which allow mutagenesis or sequence alteration by recombination of DNA sequences. With the help of standard procedures, e.g. B. Base exchanges are carried out,Partial sequences can be removed or natural or synthetic sequences can be added. Adapters or linkers can be used to connect the DNA fragments to one another, see, for example, Sambrook et al., "Mental Cloning, A Laboratory Manual, 2nd ed. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, NY; or Winnacker "Genes and Clones," VCH Weinheim, 2nd ed. 1996. The production of plant cells with an increased activity of a gene product can be achieved, for example, by the expression of at least one corresponding antisense RNA, a sense RNA to achieve a cosuppression function, or the expression of at least one appropriately constructed ribozyme that cleaves specific transcripts of the above-mentioned gene product. For this purpose, DNA molecules can be used which comprise the entire coding sequence of a gene product, including any potentially present filtering sequences, as well as DNA moleculeswhich only contain parts of the coding sequence, whereby these parts must be long enough to produce an antisense effect in the cells. It is also possible to use DNA sequences that exhibit a high degree of homology to coding sequences of a gene product, but are not completely identical. When nucleic acid molecules are expressed in plants, the synthesized protein can be expressed in any compartment of the plant cell. However, to achieve localization in a specific compartment, the coding region can be linked to DNA sequences that ensure localization in a specific compartment. Such sequences are known to the person skilled in the art (see, for example, Braun et al., EMBO J. 11 (1992), 3219-3227; Wolter et al., Proc. Natl. Acad. Sci. USA (815988), 846-850; Sonnewald et al., Plant J.1 (1),991 95-106). The expression of the nucleic acid molecules can also take place in the organelles of the plant cells. The transgenic plant cells can be regenerated into whole plants using known techniques. The transgenic plants can be plants of any desired plant species, ie both monocotyledonous and dicotyledonous plants. Thus, transgenic plants are obtainable which have altered properties such as the overexpression, suppression or inhibition of homologous (= natural) genes or gene sequences or the oxidation of heterologous (= foreign) genes or gene sequences. BCS231024-Ausland STR 81 The active ingredient combinations according to the invention can preferably be used in transgenic cultures which are tolerant or have been made tolerant to the artificial substances used. Preferably, the active compounds according to the invention can also be used in transgenic cultures which are active against growth substances,w Bie. D z.icamba or against herbicides that inhibit essential plant enzymes, e.g. B. inhibit acetolactate synthases (ALSP), PE synthases, glutamine synthases (GS), hydroxyphenylpyruvate dioxygenases (HPPD), or protophyrinogen oxidase (PPO), respectively against herbicides from the group of sulfur monomers, glyphosates, glufosinates or benzoyl isoxazoles and analogous active ingredients. The invention therefore also relates to a method for controlling undesirable plant growth, optionally in crops, preferably in non-cultivated land or in plantation crops, characterized in that one or more herbicides of type (A) are applied with one or more herbicides of type (B) to the crop plants, plant parts or plant seeds (seed) thereof or the cultivated area. The invention also relates to the use of the combinations of compounds (A)+(B) for controlling harmful plants, especially in crops,Preferably in non-cultivated land and plantation crops, but also for the control of weeds prior to sowing the following crop, in particular for sowing ("burn-down application"). The active ingredient combinations according to the invention can either be present as mixed formulations of the two components, optionally with further active ingredient additives and / or customary formulation auxiliaries, which are then applied diluted with water, or as so-called tank mixes, joint dilution of the separately formulated or partially separately formulated components with water. Compounds (A) and (B) or their combinations can be formulated in various ways, depending on the biological and / or chemical-physical parameters specified. General formulation options include, for example: wettable powders (WP), water-soluble powders (SP),Emulsifiable concentrates (rEaCt), water-soluble concentrates, aqueous solutions (SL), emulsions (EW) such as oil-in-water and water-in-oil emulsions, sprayable solutions or emulsions, oil-based dispersions, oil dispersions (OD), suspoemulsions, suspension concentrates (SC), oil-soluble solutions, capsule suspensions (CS), dusting agents (DP), seed dressings, granules for soil spreading application, granules (GR) in the form of micro-, spray, lifting and adsorption granules, water-dispersible granules (WG), water-soluble granules (SG), ULV formulation, microcapsules or waxes. The invention therefore also relates to Plant growth regulating agents containing the active ingredient combination according to the invention. The individual formulation types are described in the principle chapter and are described, for example, in: Winnacker-Küchler, "Chemische Technologie," Volume C.7 H, anser Verlag Munich, 4th ed. 1986; van Valkenburg,"Pesticide Formulations", Marcel Derk, Nke, Y., 1973; K. Martens, "Spray Drying Handbook", 3rd Ed. 1979, G. Goodwin Ltd., London. The necessary formulation aids such as inorganic materials, surfactants, solvents, and other additives are also known and are described, for example, in: Watkins, "Handbook of Insecticide Dust Diluents and Carriers", 2nd Ed., New York, Dand Books, Caldwell, NJ; H.V. Olphen, "Introduction to Clay Colloid Chemistry"; 2nd Ed., Wiley & Sons, NY; Marsden, "Solvents Guide", 2nd Ed., Interscience, NY, 1963; McCutcheon's "Drugs and Emulsifiers Annual", MC Publ. Corp., Ridgewood, NJ; Sisley and Wood, "Encyclopedi Sau orfface Active Egents", Chem. Publ. Co. Inc., NY 1964; Schönfeldt, "Interface-active ethyl hydroxyndo adducts", Wiss. Verlagsgesellschaft, Stuttgart 1976; Winnacker-Küchler, "Chemische Technologiea"n,d B 7, C. Hanser Verlag Munich,4th ed. 1986. On the basis of these formulations, combinations with other pesticidally active substances, such as other herbicides, fungicides, insecticides or other pest control agents (e.g. acaricides, nematicides, molluscicides, rodenticides, aphicides, avicides, larvicides, ovicides, bactericides, virucides, etc.), as well as safeners, fertilizers and / or growth regulators can be produced, e.g. in the form of a ready-to-use formulation or as a tablet. Wettable powders are preparations which are evenly dispersible in water and which contain, in addition to the active ingredient and a diluent or inert substance, surfactants of an ionic or non-ionic nature (wetting agents, dispersants), e.g. polyethoxylated alkylphenols, polyethoxylated fatty alcohols, polyethoxylated fatty amines, fatty alcohol polyglycol ether sulfates, alkylsulfonates, alkylbenzenesulfonates, sodium ligninsulfonate, 2,2'-dinaphthylmethane-6,6'-disulfonate, n-acetylsalicylate,dibutylnaphthalenesulfonic acid sodium or oleoylmethyltauric acid sodium enc. To produce the wettable powders, the herbicidal active ingredients are finely ground, for example, in conventional equipment such as hammer mills, fan mills, and air jet mills, and simultaneously or subsequently mixed with the formulation auxiliaries. BCS231024-Ausland STR 83 Emulsifiable concentrates are produced by dissolving the active ingredient in an organic solvent, e.g. butanol, cyclohexanone, dimethylformamide, xylene, or higher-boiling aromatics or hydrocarbons, or mixtures of the organic solvents, with the addition of one or more surfactants, ionic and / or non-ionic acids (emulsifiers). Examples of emulsifiers that can be used are: Alkylaryl folate calcium salts such as Ca- dodecylbenzenesulfonate or non-ionic emulsifiers such as fatty acid polyglycol esters, alkylaryl polyglycol ethers, fatty alcohol polyglycol ethers,Propylene oxide-ethylene oxide condensation products, alkyl polyethers, sorbitan residues, e.g., sorbitan fatty acid esters or polyoxyethylene sorbitan fatty acid esters. Dusts are obtained by grinding the dust with finely divided solid substances, e.g., talc, natural clays such as kaolin, bentonite, pyrolytic clay, or diatomaceous earth. Suspension concentrates can be based on water or oil. They can be produced, for example, by wet grinding using commercially available bead mills, with the optional addition of surfactants, such as those listed above for the other formulation types. Emulsions, e.g. oil-in-water emulsions (EW), can be prepared using stirrers, colloid mills and / or static mixers using aqueous organic solvents and, if appropriate, surfactants, such as those already listed above for the other formulation types.Granules can be produced either by spraying the product onto adsorptive, granulated inert material or by applying active ingredient concentrates to the surface of carriers such as sand, kaolinite, or granular inert material using adhesives, e.g., polyvinyl alcohol, sodium polyacrylate, or mineral oils. Suitable active ingredients can also be granulated in the manner customary for the production of fertilizer granules—if desired, mixed with fertilizers. Water-dispersible granules are produced using processes such as spray drying, fluidized-bed granulation, disc granulation, mixing with high-speed mixers, and extrusion without solid inert material. The agrochemical preparations contain, in general, 0.1 to 99% by weight, in particular 0.2 to 95% by weight, of active ingredients of types (A) and / or (B)( Depending on the type of formulation, the following concentrations are usual: BCS231024-Ausland STR 84 In wettable powders, the active ingredient concentration is, for example, about 10 to 95 wt.%, the remainder to 100 wt.% consists of usual formulation ingredients. In emulsifiable concentrates, the active ingredient concentration can be about 1 to 90 wt.%, preferably 5 to 80 wt.%. Dust-like formulations usually contain 5 to 20 wt.% of active ingredient, sprayable solutions contain about 0.05 to 80, preferably 5 to 20 wt.% active ingredient. In granules such as dispersible granules, the active ingredient content depends partly on whether the active compound is liquid or solid and whether granulating aids and fillers are used. As a rule, the content is dispersible granules between 1 and 95 wt.%,preferably between 10 and 80 wt.%. In addition, the active ingredient formulations mentioned may contain the usual adhesives, wetting agents, dispersants, emulsifiers, penetrants, grain dispersants, antifreeze agents, and solvents, fillers, dyes, and carriers, defoamers, evaporation agents, and agents that influence the pH or viscosity. For application, the formulations in commercially available form are diluted, if necessary, in the usual way, e.g., in the case of wettable powders, emulsifiable concentrates, dispersions, and water-dispersible granules, using water. Spray-formulated preparations, soil or broadcast granules, and sprayable solutions are not usually diluted with other inert substances before use. The active ingredients can be applied to the plants, plant nets, plant seeds, or the cultivated area (arable soil).preferably on thin plants and plant parts and, if necessary, also on the arable soil. One possible application is the combined use of the active ingredients in the form of tank mixes, whereby the optimally formulated combined formulations of the individual active ingredients are mixed together with water in the tank and then applied as a spray mixture. A combined herbicidal formulation of the inventive combination of active ingredients (A) and (B) has the advantage of being easier to use, as the amounts of the components are already adjusted in the correct ratio to one another. In addition, the auxiliaries in the formulation can be optimally matched to one another, whereas a tank mix of different formulations could result in undesirable combinations of auxiliaries. BCS231024-Ausland STR 85 A. General formulation examples a) A dust is obtained,by mixing 10 parts by weight (= parts by weight) of an active ingredient (A) or (B) or of an active ingredient mixture (A) + (B) (and optionally further active ingredient components) and / or their salts and 90 parts by weight of talcum powder and comminuting in a hammer mill. b) A wettable dispersion which is easily dispersible in water is obtained by mixing 25 parts by weight of an active ingredient / active ingredient mixture, 64 parts by weight of kaolin-containing quartz as an inert substance, 10 parts by weight of potassium ligninsulfonate and 1 part by weight of sodium oylmethyltaurine as a wetting and dispersing agent and milling in a pin mill. ahc) A dispersion concentrate which is easily dispersible in water is obtained by mixing 20 parts by weight of an active ingredient / active ingredient mixture with 6 parts by weight of alkylphenol polyglycol ether (®Triton X 207),3 parts by weight of isotridecanol polyglycol ether E (O8) and 71 parts by weight of paraffinic mineral oil (boiling range, for example, approx. 255 to 277 °C) are mixed and ground in a ball mill to a fineness of less than 5 microns. d) An emulsifiable concentrate is obtained from 1 part by weight of an active ingredient / active ingredient mixture, 75 parts by weight of cyclohexane as solvent, and 10 parts by weight of ethoxylated nonylphenol as emulsifier. e) Water-dispersible granules are prepared by mixing 75 parts by weight of an active ingredient / active ingredient mixture, 10 parts by weight of calcium ligninsulfonate, 5 parts by weight of sodium lauryl sulfate, 3 parts by weight of polyvinyl alcohol, and 7 parts by weight of kaolin, grinding on a pin mill, and granulating the powder in a fluidized bed by spraying water as the granulating liquid. f) Water-dispersible granules are obtained by mixing 25 parts by weight of an active ingredient / active ingredient mixture, 5 parts by weight of sodium 2,2'-dinaphthylmethane-6,6'-disulfonate,2 parts by weight of sodium oleoylmethyltaurine, 1 part by weight of polyvinyl alcohol, 17 parts by weight of calcium carbonate, and 50 parts by weight of water are homogenized and pre-comminuted in a colloid mill, then ground in a bead mill, and the resulting suspension is atomized in a spray tower with a single-component nozzle and dried. B. Biological Examples When using the combination according to the invention, herbicidal effects on a weed species are frequently observed which exceed the effects of the herbicides contained when applied alone. Alternatively, it can be observed in some cases that a lower application rate is required for the herbicide combination.to achieve the same effect on a given plant species compared to the individual preparations. Such increases in effect or effectiveness due to savings in application rate are a strong indication of synergistic effects. If the observed effect values ​​already exceed the sum of the values ​​from the trials with individual applications, then they also exceed the expected value according to Colby, which is calculated using the following formula and is also considered as an indicator of synergism (cf. SR Colby; in Weeds 15 (1967) pp. 20 to 22): E, C = A+B - (A·B / 100) Where: A = effect of the active ingredient (A) in % at an application rate of a [g ai / ha]; B = effect of the active ingredient (B) in % at an application rate of b [g ai / ha]; E C = Expected value of the effect of the combination (A(B)+) in % at the combined application rate a+b [g ai / ha]. The observed values A()E of the experiments show, at suitable low druonsgies, an effect of the combinations that exceeds the expected values ​​n Caolby (E CPost-emergence weed activity: Seeds of monocotyledonous and dicotyledonous weeds were sown in pots in sandy loam soil, covered with soil, and grown in a greenhouse under favorable growth conditions (temperature, air humidity, water supply). Three weeks after sowing, the test plants were treated with the agents according to the invention at the two- to four-leaf stage. The agents according to the invention, emulated as wettable powders or as emulsion concentrates, were sprayed onto the green plant parts at various dosages with a water application rate equivalent to 300 l / ha. After the weed plants had been in the greenhouse for three weeks under optimal growth conditions, the effectiveness of the preparations was visually assessed in comparison to untreated controls.In this context, effects of the inventive combinations were frequently observed that exceeded the formal sum of the effects when the agents were applied individually. 100% effect means complete control of each tested weed. 0% effect means no control of each tested weed at all. The biological results of the inventive combinations are summarized in Tables 3.1–3.12 below. The sum of the effects of the individual applications is shown in Tables 3.1–3.12. A given; expected values ​​according to Colby are below Cer a Engegeben; The review period is given in days after the Appliokanti (DAT). Table 3.1: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Amaranthus palmeri (AMAPA) Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.25 50 Acetochlor 450 50 150 20 A1 & Acetochlor 1 + 450 85 (E = 75) Δ = 10 1 + 150 93 (E = 85) Δ = 8 0.25 + 450 85 (E = 76) Δ = 9 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 0.0625 10 Aclonifen 30 10 A1 & Aclonifen 0.25 + 30 70 (E = 55) Δ = 15 0.0625 + 30 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 Atrazine 50 10 A1 & Atrazine 0.25 + 50 70 (E = 55) Δ = 15 BCS231024-Ausland STR 88 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.25 30 Atrazine 150 20 50 10 A1 & Atrazine 0.25 + 150 50 (E = 44) Δ = 6 0.25 + 50 60 (E = 37) Δ = 23 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 70 0.0625 10 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.0625 40 4,5-dihydro-1,2-oxazole-5-carboxylate A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-0.25 + 0.0625 100 (E = 82 Δ) = 184,5-dihydro-1,2-oxazole-5-carboxylate 0.0625 + 0.0625 70 (E = 46) Δ = 24 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.25 20 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.0625 20 4,5-dihydro-1,2-oxazole-5-carboxylate A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.25 + 0.0625 80 (E = 36 Δ) = 444,5-dihydro-1,2-oxazole-5-carboxylate Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.0625 10 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2- 0.5 85 oxazole-5-carboxylic acid A1 & 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo- 4-sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-0.0625 + 0.5 100 (E = 86.5 Δ) = 13,5oxazole-5-carboxylic acid BCS231024-Ausland STR 89 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2- 0.5 60 oxazole-5-carboxylic acid 0.125 30 A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2- 1 + 0.5 100 (E = 79) Δ = 21 oxazole-5-carboxylic acid 1 + 0.125 100 (E = 68) Δ = 32 0.25 + 0.5 80 (E = 44) Δ = 36 0.25 + 0.125 100 (E = 60) Δ = 40 0.0625 + 0.5 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.25 20 0.0625 0 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.25 88 yl]benzyliden}amino]oxy}propanoate 0.0625 70 A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.25 + 0.25 100 (E = 90.4) Δ = 9.6 yl]benzylidene}amino]oxy}propanoate 0.25 + 0.0625 88 (E = 76) Δ = 12 0.0625 + 0.25 100 (E = 88) Δ = 12 0.0625 + 0.0625 75 (E = 70) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 20 0.0625 0 Bicyclopyrone 9 60 3 50 A1 & Bicyclopyrone 0.25 + 9 80 (E = 60) Δ = 20 0.25 + 3 88 (E = 68) Δ = 20 0.0625 + 9 75 (E = 60) Δ = 15 BCS231024-Ausland STR 90 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Bicyclopyrone 9 30 3 0 A1 & Bicyclopyrone 1 + 9 75 (E = 70) Δ = 5 1 + 3 70 (E = 44) Δ = 26 0.25 + 9 40 (E = 20) Δ = 20 0.25 + 3 10 (E = 0) Δ = 10 0.0625 + 3 85 (E = 79) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.25 30 0.0625 0 Bromoxynil 240 20 80 0 A1 & Bromoxynil 0.25 + 240 50 (E = 0) Δ = 50 0.25 + 80 50 (E = 44) Δ = 6 0.0625 + 80 60 (E = 30) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 0.0625 10 Butafenacil 1 40 0.33 30 A1 & Butafenacil 0.25 + 1 85 (E = 70) Δ = 15 0.25 + 0.33 80 (E = 65) Δ = 15 0.0625 + 1 85 (E = 46) Δ = 39 0.0625 + 0.33 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.25 20 0.0625 10 Butafenacil 1 10 0.33 10 A1 & Butafenacil 0.25 + 1 60 (E = 19) Δ = 41 0.25 + 0.33 50 (E = 28) Δ = 22 0.0625 + 1 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 20 Clethodim 24 0 8 0 A1 & Clethodim 0.25 + 24 60 (E = 20) Δ = 40 0.25 + 8 75 (E = 20) Δ = 55 BCS231024-Ausland STR 91 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.0625 0 Clethodim 24 0 A1 & Clethodim 0.0625 + 24 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 85 0.25 20 0.0625 0 Dicamba 15 30 5 10 A1 & Dicamba 1 + 15 96 (E = 89.5) Δ = 6.5 0.25 + 15 88 (E = 44) Δ = 44 0.25 + 5 60 (E = 28) Δ = 32 0.0625 + 5 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Dicamba 15 30 A1 & Dicamba 1 + 15 40 (E = 30) Δ = 10 0.25 + 15 85 (E = 79) Δ = 6 0.0625 + 15 75 (E = 44) Δ = 31 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 Dimethenamid 120 20 40 10 A1 & Dimethenamid 0.25 + 120 70 (E = 60) Δ = 10 0.25 + 40 70 (E = 55) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g a.i. / ha AMAPA 21 DAT A1 0.25 20 Dimethenamid 40 10 A1 & Dimethenamid 0.25 + 40 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 85 0.25 20 Florpyrauxifen 1 60 A1 & Florpyrauxifen 1 + 1 99 (E = 94) Δ = 5 0.25 + 1 95 (E = 68) Δ = 27 BCS231024-Ausland STR 92 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 Florpyrauxifen 1 60 A1 & Florpyrauxifen 1 + 1 99 (E = 88) Δ = 11 0.25 + 1 80 (E = 68) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.25 50 0.0625 20 Flumioxazin 0.4 50 A1 & Flumioxazin 1 + 0.4 99 (E = 60) Δ = 39 0.25 + 0.4 100 (E = 85) Δ = 15 0.0625 + 0.4 99 (E = 75) Δ = 24 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 Flumioxazin 0.4 50 A1 & Flumioxazin 1 + 0.4 100 (E = 85) Δ = 15 0.25 + 0.4 85 (E = 65) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 70 Fomesafen 1.5 50 A1 & Fomesafen 1 + 1.5 97 (E = 85) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 Fomesafen 1.5 20 A1 & Fomesafen 1 + 1.5 90 (E = 76) Δ = 14 0.25 + 1.5 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 85 0.25 20 0.0625 0 Foramsulfuron 3 30 A1 & Foramsulfuron 1 + 3 60 (E = 30) Δ = 30 0.25 + 3 98 (E = 89.5) Δ = 8.5 0.0625 + 3 85 (E = 44) Δ = 41 BCS231024-Ausland STR 93 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Foramsulfuron 3 20 1 0 A1 & Foramsulfuron 1 + 3 85 (E = 76) Δ = 9 0.25 + 3 60 (E = 36) Δ = 24 0.0625 + 3 30 (E = 20) Δ = 10 0.0625 + 1 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.0625 0 Glyphosate 90 85 A1 & Glyphosate 0.0625 + 90 98 (E = 85) Δ = 13 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.0625 0 Glyphosate 90 80 A1 & Glyphosate 0.0625 + 90 97 (E = 80) Δ = 17 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 70 Icafolin-methyl 1.2 20 A1 & Icafolin-methyl 1 + 1.2 100 (E = 76) Δ = 24 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 Icafolin-methyl 1.2 50 A1 & Icafolin-methyl 1 + 1.2 100 (E = 85) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 20 0.0625 0 Indaziflam 9 30 3 20 A1 & Indaziflam 0.25 + 9 70 (E = 44) Δ = 26 0.25 + 3 60 (E = 36) Δ = 24 0.0625 + 9 60 (E = 30) Δ = 30 0.0625 + 3 30 (E = 20) Δ = 10 BCS231024-Ausland STR 94 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 85 0.25 20 Iodosulfuron 3 30 A1 & Iodosulfuron 1 + 3 97 (E = 89.5) Δ = 7.5 0.25 + 3 85 (E = 44) Δ = 41 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Iodosulfuron 3 10 A1 & Iodosulfuron 1 + 3 30 (E = 10) Δ = 20 0.25 + 3 80 (E = 73) Δ = 7 0.0625 + 3 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.0625 0 Isoxaflutole 12 80 A1 & Isoxaflutole 1 + 12 100 (E = 94) Δ = 6 0.0625 + 12 99 (E = 80) Δ = 19 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 Mesosulfuron-Methyl 1.2 30 0.4 30 A1 & Mesosulfuron-Methyl 0.25 + 1.2 80 (E = 65) Δ = 15 0.25 + 0.4 80 (E = 65) Δ = 15 Active ingredient Application rate herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 20 0.0625 0 Mesotrione 12 75 4 70 A1 & Mesotrione 0.25 + 12 98 (E = 80) Δ = 18 0.25 + 4 85 (E = 76) Δ = 9 0.0625 + 12 95 (E = 75) Δ = 20 0.0625 + 4 80 (E = 70) Δ = 10 BCS231024-Ausland STR 95 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Mesotrione 12 40 4 20 A1 & Mesotrione 1 + 12 100 (E = 76) Δ = 24 1 + 4 97 (E = 52) Δ = 45 0.25 + 12 60 (E = 36) Δ = 24 0.25 + 4 85 (E = 40) Δ = 45 0.0625 + 12 100 (E = 82) Δ = 18 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.25 50 Metribuzin 15 30 A1 & Metribuzin 0.25 + 15 80 (E = 65) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 Metribuzin 15 20 A1 & Metribuzin 1 + 15 85 (E = 76) Δ = 9 0.25 + 15 80 (E = 44) Δ = 36 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.0625 10 Oxyfluorfen 1 30 A1 & Oxyfluorfen 0.0625 + 1 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.25 30 0.0625 0 Paraquat 120 85 40 85 A1 & Paraquat 0.25 + 120 97 (E = 85) Δ = 12 0.0625 + 120 100 (E = 89.5) Δ = 10.5 0.0625 + 40 100 (E = 85) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 70 Pendimethalin 300 30 100 10 A1 & Pendimethalin 1 + 300 99 (E = 79) Δ = 20 1 + 100 85 (E = 73) Δ = 12 BCS231024-Ausland STR 96 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 Pendimethalin 300 30 100 10 A1 & Pendimethalin 1 + 300 88 (E = 79) Δ = 9 1 + 100 80 (E = 73) Δ = 7 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.25 50 Pyroxasulfone 15 10 45 30 A1 & Pyroxasulfone 1 + 15 80 (E = 55) Δ = 25 0.25 + 45 100 (E = 73) Δ = 27 0.25 + 15 70 (E = 65) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 0.0625 0 Pyroxasulfone 15 0 45 50 A1 & Pyroxasulfone 1 + 15 100 (E = 70) Δ = 30 0.25 + 45 70 (E = 65) Δ = 5 0.25 + 15 60 (E = 30) Δ = 30 0.0625 + 15 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.0625 0 Rimsulfuron 0.9 80 A1 & Rimsulfuron 0.0625 + 0.9 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.0625 0 Rimsulfuron 0.9 40 A1 & Rimsulfuron 1 + 0.9 97 (E = 82) Δ = 15 0.0625 + 0.9 60 (E = 40) Δ = 20 BCS231024-Ausland STR 97 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.25 50 0.0625 20 Saflufenacil 1.2 50 0.4 50 A1 & Saflufenacil 1 + 1.2 100 (E = 75) Δ = 25 1 + 0.4 99 (E = 75) Δ = 24 0.25 + 1.2 99 (E = 60) Δ = 39 0.25 + 0.4 98 (E = 60) Δ = 38 0.0625 + 1.2 98 (E = 85) Δ = 13 0.0625 + 0.4 100 (E = 85) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 0.0625 0 Saflufenacil 1.2 40 0.4 60 A1 & Saflufenacil 1 + 1.2 100 (E = 58) Δ = 42 1 + 0.4 85 (E = 72) Δ = 13 0.25 + 1.2 98 (E = 40) Δ = 58 0.25 + 0.4 70 (E = 60) Δ = 10 0.0625 + 1.2 93 (E = 82) Δ = 11 0.0625 + 0.4 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.25 50 S-Metolachlor 150 20 50 10 A1 & S-Metolachlor 1 + 150 99 (E = 76) Δ = 23 0.25 + 50 60 (E = 55) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 0.25 30 0.0625 0 S-Metolachlor 50 0 A1 & S-Metolachlor 0.25 + 50 40 (E = 30) Δ = 10 0.0625 + 50 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 0.0625 10 Sulfentrazone 3 50 A1 & Sulfentrazone 0.0625 + 3 75 (E = 55) Δ = 20 BCS231024-Ausland STR 98 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.25 20 Sulfentrazone 3 20 A1 & Sulfentrazone 0.25 + 3 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.25 20 Tembotrione 3 88 A1 & Tembotrione 0.25 + 3 98 (E = 90.4) Δ = 7.6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 0.0625 0 Tembotrione 3 30 9 85 A1 & Tembotrione 1 + 3 100 (E = 88) Δ = 12 0.25 + 9 88 (E = 44) Δ = 44 0.25 + 3 95 (E = 85) Δ = 10 0.0625 + 9 60 (E = 30) Δ = 30 0.0625 + 3 98 (E = 79) Δ = 19 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 0.0625 10 Terbuthylanzine 150 75 A1 & Terbuthylanzine 0.0625 + 150 99 (E = 77.5) Δ = 21.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.0625 10 Terbuthylanzine 150 30 A1 & Terbuthylanzine 0.0625 + 150 100 (E = 37) Δ = 63 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 10 DAT A1 1 85 0.25 20 0.0625 0 Thiencarbazone 0.33 10 1 30 A1 & Thiencarbazone 1 + 0.33 98 (E = 86.5) Δ = 11.5 0.25 + 1 90 (E = 44) Δ = 46 0.25 + 0.33 70 (E = 28) Δ = 42 0.0625 + 0.33 20 (E = 10) Δ = 10 BCS231024-Ausland STR 99 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 20 Thiencarbazone 0.33 20 1 30 A1 & Thiencarbazone 1 + 0.33 85 (E = 76) Δ = 9 0.25 + 1 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 0.0625 10 Tiafenacil 0.33 10 A1 & Tiafenacil 0.0625 + 0.33 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 10 DAT A1 1 70 0.0625 20 Trifludimoxazine 0.4 70 1.2 85 A1 & Trifludimoxazine 1 + 0.4 97 (E = 91) Δ = 6 0.0625 + 1.2 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA 21 DAT A1 1 70 0.25 30 0.0625 0 Trifludimoxazine 1.2 60 0.4 30 A1 & Trifludimoxazine 1 + 1.2 100 (E = 88) Δ = 12 0.25 + 1.2 80 (E = 72) Δ = 8 0.0625 + 1.2 100 (E = 60) Δ = 40 0.0625 + 0.4 50 (E = 30) Δ = 20 Table 3.2: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to resistant Amaranthus palm (AeMriAPA_R) Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 0.0625 0 2,4-D 40 20 120 50 A1 & 2,4-D 1 + 40 85 (E = 76) Δ = 9 0.25 + 120 85 (E = 55) Δ = 30 0.25 + 40 40 (E = 28) Δ = 12 0.0625 + 120 60 (E = 50) Δ = 10 BCS231024-Ausland STR 100 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 2,4-D 120 60 40 20 A1 & 2,4-D 0.25 + 120 90 (E = 64) Δ = 26 0.25 + 40 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 Aclonifen 30 10 A1 & Aclonifen 1 + 30 90 (E = 77.5) Δ = 12.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 50 Atrazine 150 40 A1 & Atrazine 0.25 + 150 75 (E = 70) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 30 0.0625 10 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6- dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.25 30 4,5-dihydro-1,2-oxazole-5-carboxylate A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.25 + 0.25 80 (E = 51) Δ = 29 4,5-dihydro-1,2-oxazole-5-carboxylate 0.0625 + 0.25 80 (E = 37) Δ = 43 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 50 0.0625 0 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.0625 10 4,5-dihydro-1,2-oxazole-5-carboxylate 0.25 20 A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 1 + 0.0625 60 (E = 55) Δ = 5 4,5-dihydro-1,2-oxazole-5-carboxylate 0.0625 + 0.25 30 (E = 20) Δ = 10 BCS231024-Ausland STR 101 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 50 0.25 20 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.125 10 5-carboxylic acid 0.5 50 A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-1 + 0.125 60 (E = 55) Δ = 55-carboxylic acid0.25 + 0.5 85 (E = 60) Δ = 25 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 10 Bicyclopyrone 9 0 3 0 A1 & Bicyclopyrone 0.25 + 9 20 (E = 10) Δ = 10 0.25 + 3 60 (E = 10) Δ = 50 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 Bicyclopyrone 3 0 A1 & Bicyclopyrone 0.25 + 3 30 (E = 10) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.0625 0 Bromoxynil 240 30 80 20 A1 & Bromoxynil 0.0625 + 240 40 (E = 30) Δ = 10 0.0625 + 80 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 30 0.0625 10 Butafenacil 1 35 0.33 25 A1 & Butafenacil 0.25 + 1 100 (E = 54.5) Δ = 45.5 0.25 + 0.33 60 (E = 47.5) Δ = 12.5 0.0625 + 1 70 (E = 41.5) Δ = 28.5 0.0625 + 0.33 50 (E = 32.5) Δ = 17.5 BCS231024-Ausland STR 102 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 30 0.0625 10 Butafenacil 1 10 A1 & Butafenacil 0.25 + 1 85 (E = 37) Δ = 48 0.0625 + 1 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 Clethodim 24 0 A1 & Clethodim 1 + 24 80 (E = 70) Δ = 10 0.25 + 24 30 (E = 10) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 0.0625 0 Clethodim 24 0 A1 & Clethodim 0.25 + 24 20 (E = 10) Δ = 10 0.0625 + 24 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 Dicamba 5 10 A1 & Dicamba 1 + 5 85 (E = 73) Δ = 12 0.25 + 5 40 (E = 19) Δ = 21 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 0.0625 0 Dicamba 15 20 A1 & Dicamba 0.25 + 15 50 (E = 28) Δ = 22 0.0625 + 15 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 Dimethenamid 120 25 40 10 A1 & Dimethenamid 1 + 120 70 (E = 47.5) Δ = 22.5 1 + 40 98 (E = 81.25) Δ = 16.75 0.25 + 120 85 (E = 77.5) Δ = 7.5 BCS231024-Ausland STR 103 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 Dimethenamid 120 30 A1 & Dimethenamid 1 + 120 98 (E = 79) Δ = 19 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 0.0625 10 Diuron 120 50 A1 & Diuron 1 + 120 70 (E = 55) Δ = 15 0.25 + 120 97 (E = 87.5) Δ = 9.5 0.0625 + 120 93 (E = 65) Δ = 28 Active ingredient Application rate Herbicides Effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 30 Diuron 120 30 A1 & Diuron 1 + 120 93 (E = 79) Δ = 14 0.25 + 120 85 (E = 51) Δ = 34 Active ingredient Application rate Herbicides Effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 0.0625 0 Florpyrauxifen 3 40 1 60 A1 & Florpyrauxifen 1 + 3 96 (E = 82) Δ = 14 1 + 1 95 (E = 88) Δ = 7 0.25 + 3 95 (E = 46) Δ = 49 0.0625 + 3 90 (E = 40) Δ = 50 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 0.0625 0 Florpyrauxifen 3 80 A1 & Florpyrauxifen 0.25 + 3 90 (E = 82) Δ = 8 0.0625 + 3 88 (E = 80) Δ = 8 BCS231024-Ausland STR 104 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 0.0625 10 Flufenacet 45 10 15 10 A1 & Flufenacet 1 + 45 99 (E = 77.5) Δ = 21.5 1 + 15 50 (E = 37) Δ = 13 0.25 + 45 50 (E = 37) Δ = 13 0.25 + 15 30 (E = 19) Δ = 11 0.0625 + 45 99 (E = 77.5) Δ = 21.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 Flufenacet 45 10 15 10 A1 & Flufenacet 1 + 45 99 (E = 73) Δ = 26 1 + 15 99 (E = 73) Δ = 26 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 50 Flufenoximacil 0.0625 60 A1 & Flufenoximacil 1 + 0.0625 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 50 0.0625 20 Flumioxazin 1.2 50 0.4 20 A1 & Flumioxazin 1 + 1.2 85 (E = 76) Δ = 9 1 + 0.4 99 (E = 60) Δ = 39 0.25 + 0.4 80 (E = 60) Δ = 20 0.0625 + 1.2 80 (E = 36) Δ = 44 0.0625 + 0.4 99 (E = 85) Δ = 14 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 50 0.0625 0 Flumioxazin 1.2 30 0.4 20 A1 & Flumioxazin 1 + 1.2 60 (E = 20) Δ = 40 0.25 + 0.4 85 (E = 79) Δ = 6 0.0625 + 0.4 100 (E = 60) Δ = 40 BCS231024-Ausland STR 105 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 0.0625 10 Fluometuron 300 25 100 20 A1 & Fluometuron 0.0625 + 300 40 (E = 32.5) Δ = 7.5 0.0625 + 100 35 (E = 28) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 50 0.0625 20 Fomesafen 4.5 40 A1 & Fomesafen 0.25 + 4.5 80 (E = 70) Δ = 10 0.0625 + 4.5 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.0625 0 Fomesafen 4.5 40 1.5 20 A1 & Fomesafen 1 + 4.5 30 (E = 20) Δ = 10 0.0625 + 4.5 98 (E = 82) Δ = 16 0.0625 + 1.5 80 (E = 40) Δ = 40 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 10 0.0625 0 Foramsulfuron 3 80 A1 & Foramsulfuron 0.25 + 3 88 (E = 82) Δ = 6 0.0625 + 3 88 (E = 80) Δ = 8 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.0625 0 Foramsulfuron 3 70 A1 & Foramsulfuron 0.0625 + 3 85 (E = 70) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 Glyphosate 90 0 30 0 A1 & Glyphosate 1 + 90 20 (E = 10) Δ = 10 0.25 + 90 85 (E = 70) Δ = 15 0.25 + 30 30 (E = 10) Δ = 20 BCS231024-Ausland STR 106 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 Icafolin-methyl 1.2 20 A1 & Icafolin-methyl 1 + 1.2 85 (E = 76) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.0625 0 Icafolin-methyl 0.4 0 A1 & Icafolin-methyl 0.0625 + 0.4 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.0625 10 Imazethapyr 2.5 25 A1 & Imazethapyr 0.0625 + 2.5 40 (E = 32.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 10 0.0625 0 Indaziflam 9 10 3 10 A1 & Indaziflam 0.25 + 9 30 (E = 19) Δ = 11 0.25 + 3 60 (E = 19) Δ = 41 0.0625 + 9 20 (E = 10) Δ = 10 0.0625 + 3 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 0.0625 0 Iodosulfuron 3 30 A1 & Iodosulfuron 1 + 3 85 (E = 30) Δ = 55 0.25 + 3 85 (E = 79) Δ = 6 0.0625 + 3 85 (E = 37) Δ = 48 Active ingredient application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 10 0.0625 0 Iodosulfuron 3 30 A1 & Iodosulfuron 0.25 + 3 80 (E = 37) Δ = 43 0.0625 + 3 85 (E = 30) Δ = 55 BCS231024-Ausland STR 107 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 0.0625 0 Isoxaflutole 12 75 4 30 A1 & Isoxaflutole 0.0625 + 12 88 (E = 75) Δ = 13 0.0625 + 4 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.0625 0 Isoxaflutole 12 70 A1 & Isoxaflutole 1 + 12 97 (E = 91) Δ = 6 0.0625 + 12 90 (E = 70) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 0.0625 10 Mesosulfuron-Methyl 1.2 50 0.4 50 A1 & Mesosulfuron-Methyl 1 + 1.2 85 (E = 65) Δ = 20 1 + 0.4 80 (E = 65) Δ = 15 0.25 + 1.2 75 (E = 55) Δ = 20 0.25 + 0.4 70 (E = 55) Δ = 15 0.0625 + 1.2 100 (E = 87.5) Δ = 12.5 0.0625 + 0.4 95 (E = 87.5) Δ = 7.5 active ingredient application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 Mesosulfuron-Methyl 1.2 20 A1 & Mesosulfuron-Methyl 1 + 1.2 100 (E = 76) Δ = 24 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 Mesotrione 12 40 4 40 A1 & Mesotrione 1 + 12 95 (E = 82) Δ = 13 0.25 + 4 80 (E = 46) Δ = 34 BCS231024-Ausland STR 108 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 10 Mesotrione 12 30 4 20 A1 & Mesotrione 1 + 12 88 (E = 79) Δ = 9 0.25 + 4 75 (E = 28) Δ = 47 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 0.0625 20 Metribuzin 45 20 A1 & Metribuzin 0.0625 + 45 45 (E = 36) Δ = 9 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 0.0625 0 Metribuzin 15 0 A1 & Metribuzin 0.0625 + 15 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 0.0625 10 Oxyfluorfen 1 20 3 35 A1 & Oxyfluorfen 1 + 1 70 (E = 54.5) Δ = 15.5 0.25 + 3 95 (E = 44) Δ = 51 0.25 + 1 60 (E = 41.5) Δ = 18.5 0.0625 + 3 60 (E = 28) Δ = 32 0.0625 + 1 95 (E = 80) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 30 Oxyfluorfen 1 10 3 20 A1 & Oxyfluorfen 1 + 1 60 (E = 37) Δ = 23 0.25 + 3 80 (E = 73) Δ = 7 0.25 + 1 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 50 0.0625 0 Paraquat 120 85 A1 & Paraquat 0.25 + 120 100 (E = 92.5) Δ = 7.5 0.0625 + 120 100 (E = 85) Δ = 15 BCS231024-Ausland STR 109 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 50 Pendimethalin 300 20 A1 & Pendimethalin 0.25 + 300 75 (E = 60) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 50 0.0625 0 Pendimethalin 300 30 A1 & Pendimethalin 0.25 + 300 70 (E = 65) Δ = 5 0.0625 + 300 50 (E = 30) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 50 0.0625 20 Pyraflufen-ethyl 30 70 10 50 A1 & Pyraflufen-ethyl 1 + 30 100 (E = 85) Δ = 15 1 + 10 85 (E = 75) Δ = 10 0.25 + 30 99 (E = 76) Δ = 23 0.25 + 10 75 (E = 60) Δ = 15 0.0625 + 30 100 (E = 91) Δ = 9 0.0625 + 10 100 (E = 85) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 50 0.0625 0 Pyraflufen-ethyl 10 40 30 85 A1 & Pyraflufen-ethyl 1 + 10 80 (E = 40) Δ = 40 0.25 + 30 100 (E = 82) Δ = 18 0.0625 + 10 100 (E = 92.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 Pyroxasulfone 45 20 15 10 A1 & Pyroxasulfone 1 + 45 85 (E = 76) Δ = 9 1 + 15 80 (E = 73) Δ = 7 BCS231024-Ausland STR 110 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 50 Saflufenacil 1.2 35 A1 & Saflufenacil 1 + 1.2 99 (E = 80.5) Δ = 18.5 0.25 + 1.2 85 (E = 67.5) Δ = 17.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 50 Saflufenacil 1.2 30 A1 & Saflufenacil 1 + 1.2 85 (E = 79) Δ = 6 0.25 + 1.2 80 (E = 65) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 0.25 50 0.0625 0 S-Metolachlor 50 0 A1 & S-Metolachlor 0.25 + 50 70 (E = 50) Δ = 20 0.0625 + 50 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 10 DAT A1 1 75 0.25 30 0.0625 10 Sulfentrazone 3 50 A1 & Sulfentrazone 1 + 3 60 (E = 55) Δ = 5 0.25 + 3 98 (E = 87.5) Δ = 10.5 0.0625 + 3 75 (E = 65) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.25 10 0.0625 0 Tembotrione 9 30 3 20 A1 & Tembotrione 1 + 9 98 (E = 76) Δ = 22 1 + 3 85 (E = 37) Δ = 48 0.25 + 9 60 (E = 28) Δ = 32 0.25 + 3 60 (E = 30) Δ = 30 0.0625 + 9 88 (E = 79) Δ = 9 BCS231024-Ausland STR 111 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.25 10 0.0625 0 Tembotrione 9 20 3 20 A1 & Tembotrione 1 + 9 85 (E = 76) Δ = 9 1 + 3 95 (E = 76) Δ = 19 0.25 + 9 75 (E = 28) Δ = 47 0.0625 + 3 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 Terbuthylanzine 150 60 A1 & Terbuthylanzine 1 + 150 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 0.25 30 0.0625 10 Tiafenacil 1 50 0.33 35 A1 & Tiafenacil 0.25 + 1 60 (E = 55) Δ = 5 0.25 + 0.33 70 (E = 65) Δ = 5 0.0625 + 1 70 (E = 54.5) Δ = 15.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AMAPA_R 10 DAT A1 1 70 0.0625 20 Trifludimoxazine 0.4 50 1.2 85 A1 & Trifludimoxazine 1 + 0.4 100 (E = 85) Δ = 15 0.0625 + 1.2 96 (E = 88) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AMAPA_R 21 DAT A1 1 70 0.0625 0 Trifludimoxazine 1.2 70 0.4 20 A1 & Trifludimoxazine 1 + 1.2 50 (E = 20) Δ = 30 1 + 0.4 100 (E = 91) Δ = 9 0.0625 + 0.4 100 (E = 76) Δ = 24 BCS231024-Ausland STR 112 Tables 3.3: Synergistic effect∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Avena fatua (AVEFA) Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 1 20 2,4-D 120 30 A1 & 2,4-D 1 + 120 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 1 20 2,4-D 120 10 A1 & 2,4-D 1 + 120 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 30 0.0625 10 Acetochlor 450 50 A1 & Acetochlor 1 + 450 70 (E = 65) Δ = 5 0.0625 + 450 60 (E = 55) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.0625 0 Acetochlor 450 40 A1 & Acetochlor 0.0625 + 450 50 (E = 40) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 0.0625 0 Atrazine 50 0 A1 & Atrazine 0.25 + 50 10 (E = 0) Δ = 10 0.0625 + 50 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 0.25 30 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.0625 20 4,5-dihydro-1,2-oxazole-5-carboxylate A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-0.25 + 0.0625 50 (E = 44 Δ) = 64,5-dihydro-1,2-oxazole-5-carboxylate BCS231024-Ausland STR 113 active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 40 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.0625 40 4,5-dihydro-1,2-oxazole-5-carboxylate A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl- 2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl- 0.25 + 0.0625 85 (E = 64 Δ) = 214,5-dihydro-1,2-oxazole-5-carboxylate Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 40 0.0625 40 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.125 30 5-carboxylic acid 0.5 40 A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-0.25 + 0.125 75 (E = 58) Δ = 175-carboxylic acid 0.0625 + 0.5 85 (E = 64) Δ = 21 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 0.0625 20 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3- methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- 0.25 40 yl]benzylidene}amino]oxy}propanoate A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)-0.0625 + 0.25 60 (E = 52 Δ) = 8yl]benzylidene}amino]oxy}propanoate Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 Bromoxynil 240 0 A1 & Bromoxynil 0.25 + 240 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 1 20 Clethodim 8 40 A1 & Clethodim 1 + 8 70 (E = 52) Δ = 18 BCS231024-Ausland STR 114 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 0.25 10 Diflufenican 120 10 A1 & Diflufenican 0.25 + 120 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 1 30 Dimethenamid 40 10 A1 & Dimethenamid 1 + 40 60 (E = 37) Δ = 23 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 70 0.25 20 Flufenacet 45 20 A1 & Flufenacet 1 + 45 85 (E = 76) Δ = 9 0.25 + 45 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 1 30 Flufenacet 45 30 A1 & Flufenacet 1 + 45 90 (E = 51) Δ = 39 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 0.25 30 0.0625 20 Flufenoximacil 0.25 40 0.0625 20 A1 & Flufenoximacil 0.25 + 0.25 60 (E = 52) Δ = 8 0.25 + 0.0625 80 (E = 58) Δ = 22 0.0625 + 0.25 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 Flumioxazin 1.2 0 0.4 0 A1 & Flumioxazin 0.25 + 1.2 10 (E = 0) Δ = 10 0.25 + 0.4 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 0.25 20 Fluometuron 300 30 100 25 A1 & Fluometuron 0.25 + 300 50 (E = 44) Δ = 6 0.25 + 100 45 (E = 40) Δ = 5 BCS231024-Ausland STR 115 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 Fomesafen 1.5 0 A1 & Fomesafen 0.25 + 1.5 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 0.0625 0 Glufosinate 90 20 A1 & Glufosinate 0.0625 + 90 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 20 Glyphosate 90 30 A1 & Glyphosate 1 + 90 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.0625 0 Glyphosate 90 10 A1 & Glyphosate 0.0625 + 90 30 (E = 10) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 30 Icafolin-methyl 1.2 60 A1 & Icafolin-methyl 1 + 1.2 98 (E = 72) Δ = 26 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 1 20 0.25 0 Icafolin-methyl 1.2 20 A1 & Icafolin-methyl 1 + 1.2 80 (E = 36) Δ = 44 0.25 + 1.2 50 (E = 20) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 1 30 Imazethapyr 2.5 20 A1 & Imazethapyr 1 + 2.5 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 0.0625 0 Indaziflam 9 0 A1 & Indaziflam 0.0625 + 9 10 (E = 0) Δ = 10 BCS231024-Ausland STR 116 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 10 0.0625 0 Iodosulfuron 3 40 A1 & Iodosulfuron 0.25 + 3 60 (E = 46) Δ = 14 0.0625 + 3 70 (E = 40) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.25 10 0.0625 0 Isoxaflutole 4 0 A1 & Isoxaflutole 0.25 + 4 20 (E = 10) Δ = 10 0.0625 + 4 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 20 0.25 10 0.0625 0 Mesotrione 4 0 A1 & Mesotrione 1 + 4 10 (E = 0) Δ = 10 0.25 + 4 30 (E = 20) Δ = 10 0.0625 + 4 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 0.25 10 Metribuzin 15 10 A1 & Metribuzin 0.25 + 15 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 1 20 0.25 0 0.0625 0 Pendimethalin 300 20 100 0 A1 & Pendimethalin 1 + 300 97 (E = 20) Δ = 77 1 + 100 70 (E = 0) Δ = 70 0.25 + 300 95 (E = 20) Δ = 75 0.25 + 100 30 (E = 0) Δ = 30 0.0625 + 300 85 (E = 36) Δ = 49 0.0625 + 100 85 (E = 20) Δ = 65 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 0.25 10 Saflufenacil 0.4 10 A1 & Saflufenacil 0.25 + 0.4 30 (E = 19) Δ = 11 BCS231024-Ausland STR 117 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 Saflufenacil 1.2 0 0.4 0 A1 & Saflufenacil 0.25 + 1.2 10 (E = 0) Δ = 10 0.25 + 0.4 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha AVEFA 10 DAT A1 0.25 10 0.0625 10 S-Metolachlor 150 10 A1 & S-Metolachlor 0.25 + 150 25 (E = 19) Δ = 6 0.0625 + 150 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 S-Metolachlor 50 0 A1 & S-Metolachlor 0.25 + 50 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 10 DAT A1 1 30 0.25 10 Trifludimoxazine 0.4 10 A1 & Trifludimoxazine 1 + 0.4 50 (E = 37) Δ = 13 0.25 + 0.4 35 (E = 19) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha AVEFA 21 DAT A1 0.25 0 0.0625 0 Trifludimoxazine 1.2 0 0.4 0 A1 & Trifludimoxazine 0.25 + 1.2 10 (E = 0) Δ = 10 0.25 + 0.4 10 (E = 0) Δ = 10 0.0625 + 1.2 10 (E = 0) Δ = 10 Table 3.4: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Bidens pilosa (BIDPI) Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 0.0625 0 2,4-D 120 80 A1 & 2,4-D 0.25 + 120 95 (E = 84) Δ = 11 0.0625 + 120 85 (E = 80) Δ = 5 BCS231024-Ausland STR 118 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.0625 0 2,4-D 120 80 A1 & 2,4-D 0.0625 + 120 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Acetochlor 150 10 450 35 A1 & Acetochlor 1 + 150 60 (E = 55) Δ = 5 0.25 + 450 55 (E = 48) Δ = 7 0.25 + 150 55 (E = 28) Δ = 27 0.0625 + 150 35 (E = 19) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.25 20 0.0625 0 Acetochlor 150 0 A1 & Acetochlor 0.25 + 150 30 (E = 20) Δ = 10 0.0625 + 150 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Atrazine 150 20 50 10 A1 & Atrazine 1 + 150 65 (E = 36) Δ = 29 1 + 50 40 (E = 28) Δ = 12 0.25 + 150 50 (E = 28) Δ = 22 0.25 + 50 30 (E = 19) Δ = 11 0.0625 + 150 98 (E = 60) Δ = 38 0.0625 + 50 96 (E = 55) Δ = 41 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 Atrazine 150 30 50 10 A1 & Atrazine 1 + 150 85 (E = 72) Δ = 13 1 + 50 85 (E = 64) Δ = 21 0.25 + 150 50 (E = 44) Δ = 6 0.0625 + 50 20 (E = 10) Δ = 10 BCS231024-Ausland STR 119 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 88 0.25 30 0.0625 20 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.0625 40 carboxylate 0.25 80 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5-1 + 0.0625 100 (E = 92.8 Δ) = 7.2carboxylate 0.25 + 0.0625 80 (E = 58) Δ = 22 0.0625 + 0.25 100 (E = 84) Δ = 16 0.0625 + 0.0625 75 (E = 52) Δ = 23 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 80 0.25 40 0.0625 10 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazol-5- 0.25 70 carboxylate 0.0625 40 A1 + Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-1 + 0.25 100 (E = 94) Δ = 6oxazole-5-carboxylate 1 + 0.0625 100 (E = 88) Δ = 12 0.25 + 0.0625 75 (E = 64) Δ = 11 0.0625 + 0.25 100 (E = 73) Δ = 27 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 0.25 30 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.5 85 5-carboxylic acid A1 & 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazol- 0.25 + 0.5 95 (E = 89.5) Δ = 5.5 5-carboxylic acid BCS231024-Ausland STR 120 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.25 40 0.0625 10 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.125 40 5-carboxylic acid A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-0.25 + 0.125 80 (E = 64) Δ = 165-carboxylic acid 0.0625+ 0.125 75 (E = 46) Δ = 29 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 88 0.25 30 0.0625 20 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- 0.0625 50 yl]benzylidene}amino]oxy}propanoate 0.25 88 A1 &Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- 1 + 0.0625 100 (E = 94) Δ = 6 yl]benzylidene}amino]oxy}propanoate 0.25 + 0.25 97 (E = 91.6) Δ = 5.4 0.25 + 0.0625 80 (E = 65) Δ = 15 0.0625 + 0.0625 75 (E = 60) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 0.25 40 0.0625 10 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.0625 40 yl]benzyliden}amino]oxy}propanoate A1 & methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)-0.25 + 0.0625 70 (E = 64 Δ) = 6yl]benzylidene}amino]oxy}propanoate 0.0625 + 0.0625 60 (E = 46) Δ = 14 BCS231024-Ausland STR 121 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 85 0.25 20 0.0625 0 Bicyclopyrone 3 20 9 20 A1 & Bicyclopyrone 1 + 3 98 (E = 88) Δ = 10 0.25 + 9 70 (E = 36) Δ = 34 0.25 + 3 80 (E = 36) Δ = 44 0.0625 + 9 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 70 0.25 20 0.0625 0 Bicyclopyrone 3 10 9 10 A1 & Bicyclopyrone 1 + 3 30 (E = 10) Δ = 20 0.25 + 9 99 (E = 73) Δ = 26 0.0625 + 9 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Bromoxynil 240 70 80 50 A1 & Bromoxynil 1 + 240 95 (E = 85) Δ = 10 1 + 80 90 (E = 75) Δ = 15 0.25 + 240 100 (E = 76) Δ = 24 0.0625 + 240 85 (E = 73) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 Bromoxynil 80 40 240 70 A1 & Bromoxynil 1 + 80 85 (E = 76) Δ = 9 0.25 + 240 100 (E = 76) Δ = 24 BCS231024-Ausland STR 122 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 75 0.25 30 0.0625 10 Butafenacil 1 35 0.33 20 A1 & Butafenacil 1 + 1 95 (E = 80) Δ = 15 1 + 0.33 70 (E = 54.5) Δ = 15.5 0.25 + 1 50 (E = 44) Δ = 6 0.25 + 0.33 35 (E = 28) Δ = 7 0.0625 + 0.33 95 (E = 83.75) Δ = 11.25 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 30 Butafenacil 1 10 0.33 10 A1 & Butafenacil 1 + 1 80 (E = 37) Δ = 43 1 + 0.33 80 (E = 37) Δ = 43 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 Clethodim 8 0 A1 & Clethodim 0.25 + 8 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 70 0.25 20 0.0625 0 Clethodim 8 0 24 10 A1 & Clethodim 1 + 8 80 (E = 70) Δ = 10 0.25 + 8 30 (E = 20) Δ = 10 0.0625 + 24 20 (E = 10) Δ = 10 0.0625 + 8 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 0.0625 0 Dicamba 15 30 5 20 A1 & Dicamba 0.25 + 15 40 (E = 30) Δ = 10 0.25 + 5 85 (E = 44) Δ = 41 0.0625 + 15 70 (E = 36) Δ = 34 BCS231024-Ausland STR 123 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.25 20 Dicamba 15 50 5 30 A1 & Dicamba 0.25 + 15 80 (E = 60) Δ = 20 0.25 + 5 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 Diflufenican 120 35 A1 & Diflufenican 1 + 120 80 (E = 67.5) Δ = 12.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 Diflufenican 120 30 A1 & Diflufenican 1 + 120 80 (E = 72) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 75 Dimethenamid 40 10 A1 & Dimethenamid 1 + 40 85 (E = 77.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 30 Dimethenamid 40 10 A1 & Dimethenamid 1 + 40 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 0.25 30 Diuron 120 20 A1 & Diuron 0.25 + 120 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 30 Diuron 120 10 40 10 A1 & Diuron 1 + 120 50 (E = 37) Δ = 13 1 + 40 50 (E = 37) Δ = 13 BCS231024-Ausland STR 124 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 85 0,25 20 0,0625 0 Florpyrauxifen 3 40 1 30 A1 & Florpyrauxifen 1 + 3 97 (E = 91) Δ = 6 0,25 + 3 95 (E = 52) Δ = 43 0,25 + 1 80 (E = 44) Δ = 36 0,0625 + 3 70 (E = 40) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 70 0,25 20 0,0625 0 Florpyrauxifen 3 40 1 20 A1 & Florpyrauxifen 1 + 3 85 (E = 76) Δ = 9 1 + 1 60 (E = 52) Δ = 8 0.25 + 3 80 (E = 36) Δ = 44 0.25 + 1 50 (E = 40) Δ = 10 0.0625 + 3 88 (E = 82) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 0.0625 10 Flufenacet 15 10 A1 & Flufenacet 0.0625 + 15 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 30 Flufenacet 45 10 A1 & Flufenacet 1 + 45 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 80 0.0625 10 Flufenoximacil 0.0625 75 0.25 85 A1 & Flufenoximacil 1 + 0.0625 100 (E = 95) Δ = 5 0.0625 + 0.25 95 (E = 86.5) Δ = 8.5 BCS231024-Ausland STR 125 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Flumioxazin 0.4 50 1.2 50 A1 & Flumioxazin 1 + 0.4 99 (E = 75) Δ = 24 0.25 + 1.2 75 (E = 60) Δ = 15 0.25 + 0.4 70 (E = 60) Δ = 10 0.0625 + 1.2 60 (E = 55) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 30 Fluometuron 100 10 A1 & Fluometuron 1 + 100 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Fomesafen 4.5 50 1.5 50 A1 & Fomesafen 1 + 4.5 93 (E = 60) Δ = 33 1 + 1.5 75 (E = 60) Δ = 15 0.25 + 4.5 65 (E = 55) Δ = 10 0.25 + 1.5 70 (E = 55) Δ = 15 0.0625 + 4.5 99 (E = 75) Δ = 24 0.0625 + 1.5 85 (E = 75) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 Fomesafen 4.5 20 4.5 20 A1 & Fomesafen 1 + 4.5 40 (E = 20) Δ = 20 0.25 + 4.5 98 (E = 68) Δ = 30 0.0625 + 4.5 97 (E = 36) Δ = 61 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 0.25 20 0.0625 0 Foramsulfuron 3 60 1 40 A1 & Foramsulfuron 0.25 + 3 70 (E = 60) Δ = 10 0.25 + 1 80 (E = 68) Δ = 12 0.0625 + 3 60 (E = 52) Δ = 8 BCS231024-Ausland STR 126 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.0625 0 Glyphosate 90 90 A1 & Glyphosate 0.0625 + 90 95 (E = 90) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Icafolin-methyl 1.2 10 0.4 10 A1 & Icafolin-methyl 1 + 1.2 50 (E = 28) Δ = 22 1 + 0.4 50 (E = 28) Δ = 22 0.25 + 1.2 30 (E = 19) Δ = 11 0.25 + 0.4 25 (E = 19) Δ = 6 0.0625 + 1.2 70 (E = 55) Δ = 15 0.0625 + 0.4 75 (E = 55) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 Icafolin-methyl 1.2 10 0.4 0 A1 & Icafolin-methyl 1 + 1.2 70 (E = 64) Δ = 6 1 + 0.4 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 0.0625 0 Isoxaflutole 12 60 A1 & Isoxaflutole 0.25 + 12 88 (E = 68) Δ = 20 0.0625 + 12 88 (E = 60) Δ = 28 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 70 Isoxaflutole 4 30 A1 & Isoxaflutole 1 + 4 88 (E = 79) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 0.25 30 Mesosulfuron-Methyl 1.2 50 A1 & Mesosulfuron-Methyl 0.25 + 1.2 80 (E = 65) Δ = 15 BCS231024-Ausland STR 127 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 30 Mesosulfuron-Methyl 1.2 20 A1 & Mesosulfuron-Methyl 1 + 1.2 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 0.0625 0 Mesotrione 12 60 4 50 A1 & Mesotrione 0.25 + 12 80 (E = 60) Δ = 20 0.25 + 4 88 (E = 68) Δ = 20 0.0625 + 12 80 (E = 60) Δ = 20 Active ingredient application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 70 0.25 20 0.0625 0 Mesotrione 12 30 A1 & Mesotrione 1 + 12 60 (E = 30) Δ = 30 0.25 + 12 88 (E = 79) Δ = 9 0.0625 + 12 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Metribuzin 45 30 15 20 A1 & Metribuzin 1 + 45 80 (E = 60) Δ = 20 1 + 15 70 (E = 44) Δ = 26 0.25 + 45 50 (E = 36) Δ = 14 0.25 + 15 60 (E = 37) Δ = 23 0.0625 + 45 85 (E = 65) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.0625 0 Metribuzin 45 30 15 20 A1 & Metribuzin 0.0625 + 45 40 (E = 30) Δ = 10 0.0625 + 15 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 30 Oxyfluorfen 3 10 A1 & Oxyfluorfen 1 + 3 50 (E = 37) Δ = 13 BCS231024-Ausland STR 128 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 Paraquat 40 75 A1 & Paraquat 1 + 40 99 (E = 87.5) Δ = 11.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 0.25 20 Paraquat 40 50 A1 & Paraquat 0.25 + 40 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Pendimethalin 100 10 300 10 A1 & Pendimethalin 1 + 100 80 (E = 55) Δ = 25 0.25 + 300 40 (E = 28) Δ = 12 0.25 + 100 50 (E = 28) Δ = 22 0.0625 + 300 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 Pendimethalin 100 0 A1 & Pendimethalin 1 + 100 80 (E = 60) Δ = 20 0.25 + 100 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 Pyraflufen-ethyl 10 80 A1 & Pyraflufen-ethyl 1 + 10 85 (E = 80) Δ = 5 0.25 + 10 100 (E = 92) Δ = 8 0.0625 + 10 100 (E = 84) Δ = 16 BCS231024-Ausland STR 129 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Pyroxasulfone 45 20 15 10 A1 & Pyroxasulfone 1 + 45 50 (E = 36) Δ = 14 1 + 15 50 (E = 28) Δ = 22 0.25 + 45 35 (E = 28) Δ = 7 0.25 + 15 35 (E = 19) Δ = 16 0.0625 + 45 70 (E = 60) Δ = 10 0.0625 + 15 75 (E = 55) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 Pyroxasulfone 15 0 A1 & Pyroxasulfone 1 + 15 70 (E = 60) Δ = 10 0.25 + 15 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Saflufenacil 1.2 75 0.4 50 A1 & Saflufenacil 1 + 1.2 99 (E = 80) Δ = 19 1 + 0.4 90 (E = 60) Δ = 30 0.25 + 1.2 90 (E = 77.5) Δ = 12.5 0.25 + 0.4 70 (E = 55) Δ = 15 0.0625 + 1.2 100 (E = 87.5) Δ = 12.5 0.0625 + 0.4 96 (E = 75) Δ = 21 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 Saflufenacil 1.2 40 0.4 30 A1 & Saflufenacil 1 + 1.2 85 (E = 72) Δ = 13 1 + 0.4 85 (E = 52) Δ = 33 0.25 + 1.2 80 (E = 44) Δ = 36 0.25 + 0.4 70 (E = 40) Δ = 30 0.0625 + 1.2 100 (E = 76) Δ = 24 BCS231024-Ausland STR 130 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 S-Metolachlor 150 20 50 10 A1 & S-Metolachlor 1 + 150 50 (E = 36) Δ = 14 1 + 50 50 (E = 28) Δ = 22 0.25 + 150 35 (E = 28) Δ = 7 0.25 + 50 30 (E = 19) Δ = 11 0.0625 + 150 95 (E = 60) Δ = 35 0.0625 + 50 70 (E = 55) Δ = 15 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 S-Metolachlor 150 20 50 0 A1 & S-Metolachlor 1 + 150 20 (E = 0) Δ = 20 0.25 + 50 80 (E = 68) Δ = 12 0.0625 + 50 40 (E = 20) Δ = 20 Active ingredient application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 0.25 20 0.0625 0 Tembotrione 9 20 3 10 A1 & Tembotrione 0.25 + 9 80 (E = 36) Δ = 44 0.25 + 3 75 (E = 28) Δ = 47 0.0625 + 9 40 (E = 20) Δ = 20 0.0625 + 3 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 21 DAT A1 1 70 0.25 20 0.0625 0 Tembotrione 3 0 9 20 A1 & Tembotrione 1 + 3 50 (E = 36) Δ = 14 0.25 + 9 40 (E = 20) Δ = 20 0.25 + 3 30 (E = 20) Δ = 10 0.0625 + 9 10 (E = 0) Δ = 10 0.0625 + 3 85 (E = 70) Δ = 15 BCS231024-Ausland STR 131 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 75 0.25 30 Terbuthylanzine 50 30 150 35 A1 & Terbuthylanzine 1 + 50 90 (E = 82.5) Δ = 7.5 0.25 + 150 70 (E = 54.5) Δ = 15.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 30 0.0625 10 Terbuthylanzine 150 10 50 10 A1 & Terbuthylanzine 1 + 150 30 (E = 19) Δ = 11 1 + 50 60 (E = 37) Δ = 23 0.0625 + 150 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BIDPI 10 DAT A1 1 75 0.25 30 0.0625 10 Tiafenacil 1 50 A1 & Tiafenacil 1 + 1 85 (E = 55) Δ = 30 0.25 + 1 100 (E = 87.5) Δ = 12.5 0.0625 + 1 90 (E = 65) Δ = 25 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 30 0.25 20 0.0625 10 Tiafenacil 1 25 A1 & Tiafenacil 1 + 1 50 (E = 32.5) Δ = 17.5 0.25 + 1 100 (E = 47.5) Δ = 52.5 0.0625 + 1 70 (E = 40) Δ = 30 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 10 DAT A1 1 50 0.25 20 0.0625 10 Trifludimoxazine 1.2 60 0.4 55 A1 & Trifludimoxazine 1 + 1.2 100 (E = 77.5) Δ = 22.5 1 + 0.4 80 (E = 68) Δ = 12 0.25 + 1.2 75 (E = 64) Δ = 11 0.25 + 0.4 80 (E = 64) Δ = 16 0.0625 + 1.2 85 (E = 80) Δ = 5 BCS231024-Ausland STR 132 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BIDPI 21 DAT A1 1 60 0.25 20 0.0625 0 Trifludimoxazine 0.4 20 1.2 30 A1 & Trifludimoxazine 1 + 0.4 50 (E = 44) Δ = 6 0.25 + 1.2 50 (E = 36) Δ = 14 0.25 + 0.4 40 (E = 30) Δ = 10 0.0625 + 1.2 40 (E = 20) Δ = 20 0.0625 + 0.4 98 (E = 68) Δ = 30 Table 3.5: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Brachiaria platyphylla (BRAPP) Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 40 2,4-D 120 10 A1 & 2,4-D 1 + 120 88 (E = 46) Δ = 42 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 2,4-D 120 0 A1 & 2,4-D 1 + 120 85 (E = 40) Δ = 45 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 60 0.25 40 0.0625 40 Acetochlor 450 50 150 20 A1 & Acetochlor 1 + 450 96 (E = 68) Δ = 28 1 + 150 95 (E = 70) Δ = 25 0.25 + 450 93 (E = 52) Δ = 41 0.25 + 150 95 (E = 70) Δ = 25 0.0625 + 450 98 (E = 80) Δ = 18 BCS231024-Ausland STR 133 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 20 Acetochlor 150 20 450 80 A1 & Acetochlor 1 + 150 80 (E = 52) Δ = 28 0.25 + 450 93 (E = 84) Δ = 9 0.25 + 150 70 (E = 36) Δ = 34 0.0625 + 450 95 (E = 84) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 0.25 10 Aclonifen 90 20 A1 & Aclonifen 0.25 + 90 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 0.25 20 0.0625 20 Atrazine 50 0 A1 & Atrazine 0.25 + 50 30 (E = 20) Δ = 10 0.0625 + 50 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 0.0625 40 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.25 40 carboxylate A1 + Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-0.0625 + 0.25 80 (E = 64 Δ) = 16oxazole-5-carboxylateActive ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 0.25 40 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.25 40 carboxylate A1 + Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 0.25 + 0.25 75 (E = 64) Δ = 11 oxazole-5-carboxylate BCS231024-Ausland STR 134 active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 60 0.25 40 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.5 40 5-carboxylic acid 0.125 30 A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 1 + 0.5 85 (E = 64) Δ = 21 5-carboxylic acid1 + 0.125 100 (E = 76) Δ = 24 0.25 + 0.5 100 (E = 72) Δ = 28 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 0.25 20 Bicyclopyrone 3 60 A1 & Bicyclopyrone 0.25 + 3 80 (E = 68) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 Bicyclopyrone 3 20 A1 & Bicyclopyrone 1 + 3 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 Butafenacil 1 30 0.33 10 A1 & Butafenacil 1 + 1 75 (E = 51) Δ = 24 1 + 0.33 70 (E = 37) Δ = 33 0.25 + 1 70 (E = 37) Δ = 33 0.25 + 0.33 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 20 Butafenacil 0.33 10 A1 & Butafenacil 1 + 0.33 40 (E = 28) Δ = 12 BCS231024-Ausland STR 135 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 10 Clethodim 8 88 A1 & Clethodim 1 + 8 98 (E = 89.2) Δ = 8.8 0.25 + 8 100 (E = 92.8) Δ = 7.2 0.0625 + 8 97 (E = 90.4) Δ = 6.6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 40 Dicamba 15 10 A1 & Dicamba 1 + 15 75 (E = 46) Δ = 29 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 Dicamba 15 0 5 0 A1 & Dicamba 1 + 15 60 (E = 40) Δ = 20 0.25 + 5 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 Diflufenican 360 0 A1 & Diflufenican 1 + 360 70 (E = 40) Δ = 30 0.25 + 360 60 (E = 20) Δ = 40 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 Dimethenamid 40 10 120 10 A1 & Dimethenamid 1 + 40 30 (E = 19) Δ = 11 0.25 + 120 70 (E = 37) Δ = 33 0.25 + 40 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 20 Dimethenamid 120 10 40 10 A1 & Dimethenamid 1 + 120 40 (E = 28) Δ = 12 1 + 40 35 (E = 28) Δ = 7 BCS231024-Ausland STR 136 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 0.25 10 0.0625 10 Diuron 120 30 A1 & Diuron 0.25 + 120 50 (E = 37) Δ = 13 0.0625 + 120 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 40 Florpyrauxifen 3 20 A1 & Florpyrauxifen 1 + 3 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 Florpyrauxifen 1 30 A1 & Florpyrauxifen 1 + 1 70 (E = 58) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 30 Flufenacet 45 20 15 10 A1 & Flufenacet 1 + 45 50 (E = 44) Δ = 6 1 + 15 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 0.25 10 Flufenacet 45 10 A1 & Flufenacet 0.25 + 45 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 0.25 70 0.0625 40 Flufenoximacil 0.25 80 A1 & Flufenoximacil 0.25 + 0.25 100 (E = 94) Δ = 6 0.0625 + 0.25 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 60 0.25 40 0.0625 20 Flufenoximacil 0.25 60 A1 & Flufenoximacil 1 + 0.25 100 (E = 68) Δ = 32 0.25 + 0.25 100 (E = 84) Δ = 16 0.0625 + 0.25 100 (E = 76) Δ = 24 BCS231024-Ausland STR 137 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 60 0.0625 40 Flumioxazin 1.2 50 A1 & Flumioxazin 1 + 1.2 85 (E = 80) Δ = 5 0.0625 + 1.2 93 (E = 70) Δ = 23 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.0625 20 Flumioxazin 0.4 30 1.2 60 A1 & Flumioxazin 1 + 0.4 70 (E = 58) Δ = 12 0.0625 + 1.2 85 (E = 68) Δ = 17 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 Fluometuron 100 40 A1 & Fluometuron 1 + 100 75 (E = 58) Δ = 17 0.25 + 100 60 (E = 46) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 Fomesafen 1.5 20 A1 & Fomesafen 1 + 1.5 70 (E = 52) Δ = 18 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 40 0.25 20 0.0625 10 Glufosinate 30 40 A1 & Glufosinate 1 + 30 88 (E = 46) Δ = 42 0.25 + 30 88 (E = 64) Δ = 24 0.0625 + 30 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 40 0.25 20 0.0625 10 Glyphosate 90 88 30 60 A1 & Glyphosate 1 + 90 100 (E = 92.8) Δ = 7.2 1 + 30 85 (E = 76) Δ = 9 0.25 + 30 88 (E = 68) Δ = 20 0.0625 + 30 88 (E = 64) Δ = 24 BCS231024-Ausland STR 138 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 10 Glyphosate 90 88 30 0 A1 & Glyphosate 1 + 90 100 (E = 92.8) Δ = 7.2 1 + 30 60 (E = 40) Δ = 20 0.25 + 30 88 (E = 20) Δ = 68 0.0625 + 30 60 (E = 10) Δ = 50 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 0.25 10 0.0625 10 Imazethapyr 2.5 60 A1 & Imazethapyr 0.25 + 2.5 70 (E = 64) Δ = 6 0.0625 + 2.5 70 (E = 64) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 40 0.0625 10 Indaziflam 9 20 3 10 A1 & Indaziflam 1 + 9 60 (E = 52) Δ = 8 0.0625 + 3 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 10 Indaziflam 9 30 3 10 A1 & Indaziflam 1 + 9 30 (E = 19) Δ = 11 0.25 + 3 85 (E = 58) Δ = 27 0.0625 + 3 70 (E = 28) Δ = 42 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 40 Iodosulfuron 3 30 1 20 A1 & Iodosulfuron 1 + 3 80 (E = 58) Δ = 22 1 + 1 80 (E = 52) Δ = 28 BCS231024-Ausland STR 139 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 Mesosulfuron-Methyl 0.4 30 A1 & Mesosulfuron-Methyl 1 + 0.4 70 (E = 51) Δ = 19 0.25 + 0.4 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 20 0.25 10 Mesosulfuron-Methyl 0.4 10 A1 & Mesosulfuron-Methyl 1 + 0.4 50 (E = 28) Δ = 22 0.25 + 0.4 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 40 Mesotrione 12 88 A1 & Mesotrione 1 + 12 100 (E = 92.8) Δ = 7.2 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 10 Mesotrione 12 70 A1 & Mesotrione 1 + 12 85 (E = 73) Δ = 12 0.25 + 12 100 (E = 82) Δ = 18 0.0625 + 12 85 (E = 76) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 0.0625 20 Metribuzin 45 70 A1 & Metribuzin 0.0625 + 45 85 (E = 76) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 Oxadiazon 60 30 20 20 A1 & Oxadiazon 1 + 60 60 (E = 37) Δ = 23 1 + 20 75 (E = 51) Δ = 24 0.25 + 60 50 (E = 44) Δ = 6 BCS231024-Ausland STR 140 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 20 Oxadiazon 60 20 A1 & Oxadiazon 1 + 60 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 30 0.25 10 0.0625 10 Oxyfluorfen 3 20 1 10 A1 & Oxyfluorfen 1 + 3 80 (E = 37) Δ = 43 1 + 1 50 (E = 28) Δ = 22 0.25 + 3 40 (E = 19) Δ = 21 0.25 + 1 40 (E = 28) Δ = 12 0.0625 + 3 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 20 Oxyfluorfen 1 10 A1 & Oxyfluorfen 1 + 1 35 (E = 28) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 0.25 40 Paraquat 40 80 A1 & Paraquat 0.25 + 40 97 (E = 88) Δ = 9 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 20 Paraquat 120 70 A1 & Paraquat 1 + 120 85 (E = 76) Δ = 9 0.25 + 120 93 (E = 82) Δ = 11 0.0625 + 120 85 (E = 76) Δ = 9 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 Pendimethalin 100 0 A1 & Pendimethalin 1 + 100 50 (E = 40) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 0.0625 40 Pyraflufen-ethyl 10 70 A1 & Pyraflufen-ethyl 0.0625 + 10 99 (E = 82) Δ = 17 BCS231024-Ausland STR 141 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 0.25 20 Pyraflufen-ethyl 30 60 A1 & Pyraflufen-ethyl 0.25 + 30 80 (E = 68) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 60 Pyroxasulfone 45 80 A1 & Pyroxasulfone 1 + 45 98 (E = 92) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 1 60 0.25 40 Saflufenacil 1.2 30 A1 & Saflufenacil 1 + 1.2 93 (E = 72) Δ = 21 0.25 + 1.2 90 (E = 58) Δ = 32 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 Saflufenacil 1.2 0 0.4 0 A1 & Saflufenacil 1 + 1.2 80 (E = 20) Δ = 60 1 + 0.4 85 (E = 40) Δ = 45 0.25 + 1.2 60 (E = 40) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 10 DAT A1 1 60 S-Metolachlor 150 25 A1 & S-Metolachlor 1 + 150 96 (E = 70) Δ = 26 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 20 S-Metolachlor 150 0 50 0 A1 & S-Metolachlor 1 + 150 70 (E = 20) Δ = 50 0.25 + 150 80 (E = 20) Δ = 60 0.25 + 50 50 (E = 20) Δ = 30 0.0625 + 150 80 (E = 20) Δ = 60 0.0625 + 50 88 (E = 40) Δ = 48 BCS231024-Ausland STR 142 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 0.25 10 0.0625 10 Sulfentrazone 3 10 A1 & Sulfentrazone 0.25 + 3 30 (E = 19) Δ = 11 0.0625 + 3 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 0.25 20 0.0625 10 Tembotrione 3 60 A1 & Tembotrione 0.25 + 3 80 (E = 68) Δ = 12 0.0625 + 3 85 (E = 64) Δ = 21 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 10 Tembotrione 3 20 9 70 A1 & Tembotrione 1 + 3 60 (E = 52) Δ = 8 0.25 + 3 60 (E = 36) Δ = 24 0.0625 + 9 85 (E = 73) Δ = 12 0.0625 + 3 60 (E = 28) Δ = 32 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 10 DAT A1 0.25 20 0.0625 10 Thiencarbazone 0.33 90 A1 & Thiencarbazone 0.25 + 0.33 98 (E = 92) Δ = 6 0.0625 + 0.33 98 (E = 91) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha BRAPP 21 DAT A1 1 20 0.25 10 Tiafenacil 1 30 0.33 20 A1 & Tiafenacil 1 + 1 60 (E = 44) Δ = 16 1 + 0.33 60 (E = 36) Δ = 24 0.25 + 1 50 (E = 37) Δ = 13 0.25 + 0.33 40 (E = 28) Δ = 12 BCS231024-Ausland STR 143 Active ingredient Application rate Herbicidal effect [%] against g ai / ha BRAPP 21 DAT A1 1 40 0.25 20 0.0625 20 Trifludimoxazine 1.2 40 0.4 0 A1 & Trifludimoxazine 1 + 1.2 50 (E = 40) Δ = 10 1 + 0.4 70 (E = 52) Δ = 18 0.25 + 1.2 40 (E = 20) Δ = 20 0.25 + 0.4 50 (E = 20) Δ = 30 0.0625 + 0.4 80 (E = 64) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against BRAPP 10 g ai / ha DAT A1 0.15 85 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3-[(S)-methylsulfinyl]-4- 2 40 (trifluoromethyl)benzamide A1 + 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3-[(S)-methylsulfinyl]-4- 0.15 + 2 95 (E = 91) Δ = 4 (trifluoromethyl)benzamide Table 3.6: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Centaurea cyanus (CENCY) Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.0625 0 2,4-D 120 80 40 80 A1 & 2,4-D 0.0625 + 120 85 (E = 80) Δ = 5 0.0625 + 40 88 (E = 80) Δ = 8 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Acetochlor 450 20 A1 & Acetochlor 0.0625 + 450 30 (E = 20) Δ = 10 BCS231024-Ausland STR 144 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Aclonifen 90 10 30 10 A1 & Aclonifen 0.25 + 90 50 (E = 37) Δ = 13 0.25 + 30 98 (E = 37) Δ = 61 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 1 80 Atrazine 50 10 A1 & Atrazine 1 + 50 93 (E = 82) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 60 0.0625 20 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.25 88 carboxylate A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-0.25 + 0.25 100 (E = 95.2 Δ) = 4,8oxazole-5-carboxylate 0.0625 + 0.25 100 (E = 90.4) Δ = 9.6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.25 60 0.0625 20 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.5 88 5-carboxylic acid 0.125 85 A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.25 + 0.5 100 (E = 90.4) Δ = 9.6 5-carboxylic acid 0.25 + 0.125 100 (E = 95.2) Δ = 4.8 0.0625 + 0.5 100 (E = 94) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.25 20 0.0625 0 Bicyclopyrone 9 40 A1 & Bicyclopyrone 0.25 + 9 80 (E = 52) Δ = 28 0.0625 + 9 60 (E = 40) Δ = 20 BCS231024-Ausland STR 145 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 50 Bromoxynil 240 60 A1 & Bromoxynil 0.25 + 240 98 (E = 80) Δ = 18 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Bromoxynil 240 20 80 10 A1 & Bromoxynil 0.0625 + 240 50 (E = 20) Δ = 30 0.0625 + 80 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 10 Butafenacil 1 60 0.33 20 A1 & Butafenacil 0.25 + 1 93 (E = 64) Δ = 29 0.25 + 0.33 98 (E = 72) Δ = 26 0.0625 + 1 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.25 20 0.0625 10 Butafenacil 1 40 A1 & Butafenacil 0.25 + 1 99 (E = 52) Δ = 47 0.0625 + 1 85 (E = 46) Δ = 39 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 1 88 0.25 30 Clethodim 24 10 8 0 A1 & Clethodim 1 + 24 60 (E = 30) Δ = 30 1 + 8 97 (E = 89.2) Δ = 7.8 0.25 + 8 97 (E = 88) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 1 80 Clethodim 24 0 8 0 A1 & Clethodim 1 + 24 98 (E = 80) Δ = 18 1 + 8 88 (E = 80) Δ = 8 BCS231024-Ausland STR 146 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 0 Dicamba 15 30 5 20 A1 & Dicamba 0.25 + 15 30 (E = 20) Δ = 10 0.25 + 5 88 (E = 51) Δ = 37 0.0625 + 5 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 1 80 0.25 20 Dicamba 15 40 A1 & Dicamba 1 + 15 95 (E = 88) Δ = 7 0.25 + 15 80 (E = 52) Δ = 28 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Diflufenican 360 0 A1 & Diflufenican 0.0625 + 360 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Dimethenamid 120 10 A1 & Dimethenamid 0.25 + 120 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Diuron 120 20 A1 & Diuron 0.25 + 120 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Florpyrauxifen 3 90 A1 & Florpyrauxifen 0.0625 + 3 97 (E = 90) Δ = 7 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.0625 10 Flufenacet 15 10 A1 & Flufenacet 0.0625 + 15 30 (E = 19) Δ = 11 BCS231024-Ausland STR 147 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 50 Flumioxazin 1.2 30 A1 & Flumioxazin 0.25 + 1.2 75 (E = 65) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Fluometuron 300 30 A1 & Fluometuron 0.25 + 300 75 (E = 51) Δ = 24 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.25 20 Fluometuron 300 30 A1 & Fluometuron 0.25 + 300 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 1 80 Fomesafen 1.5 20 A1 & Fomesafen 1 + 1.5 90 (E = 84) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Fomesafen 1.5 0 A1 & Fomesafen 0.0625 + 1.5 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 0 Glufosinate 90 60 A1 & Glufosinate 0.25 + 90 97 (E = 72) Δ = 25 0.0625 + 90 99 (E = 60) Δ = 39 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.25 20 0.0625 0 Glufosinate 90 20 A1 & Glufosinate 0.25 + 90 85 (E = 36) Δ = 49 0.0625 + 90 100 (E = 20) Δ = 80 BCS231024-Ausland STR 148 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 0 Glyphosate 90 40 30 20 A1 & Glyphosate 0.25 + 90 80 (E = 58) Δ = 22 0.25 + 30 75 (E = 44) Δ = 31 0.0625 + 90 60 (E = 40) Δ = 20 0.0625 + 30 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Glyphosate 90 20 A1 & Glyphosate 0.0625 + 90 40 (E = 20) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 1 80 0.25 50 Icafolin-methyl 1.2 10 0.4 10 A1 & Icafolin-methyl 1 + 1.2 80 (E = 55) Δ = 25 1 + 0.4 100 (E = 82) Δ = 18 0.25 + 1.2 98 (E = 82) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 1 80 0.0625 0 Icafolin-methyl 1.2 0 0.4 0 A1 & Icafolin-methyl 1 + 1.2 20 (E = 0) Δ = 20 1 + 0.4 98 (E = 80) Δ = 18 0.0625 + 0.4 98 (E = 80) Δ = 18 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Imazethapyr 2.5 10 A1 & Imazethapyr 0.25 + 2.5 60 (E = 37) Δ = 23 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Indaziflam 3 30 A1 & Indaziflam 0.25 + 3 80 (E = 51) Δ = 29 BCS231024-Ausland STR 149 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 1 80 Indaziflam 3 20 A1 & Indaziflam 1 + 3 97 (E = 84) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.0625 0 Iodosulfuron 3 80 1 80 A1 & Iodosulfuron 0.0625 + 3 88 (E = 80) Δ = 8 0.0625 + 1 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Iodosulfuron 3 70 A1 & Iodosulfuron 0.0625 + 3 75 (E = 70) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 0 Isoxaflutole 12 30 A1 & Isoxaflutole 0.25 + 12 70 (E = 51) Δ = 19 0.0625 + 12 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 10 Mesosulfuron-Methyl 1.2 50 0.4 50 A1 & Mesosulfuron-Methyl 0.25 + 1.2 75 (E = 55) Δ = 20 0.25 + 0.4 93 (E = 65) Δ = 28 0.0625 + 1.2 70 (E = 65) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.0625 0 Mesotrione 12 80 4 75 A1 & Mesotrione 0.0625 + 12 88 (E = 80) Δ = 8 0.0625 + 4 88 (E = 75) Δ = 13 BCS231024-Ausland STR 150 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 1 80 0.0625 0 Mesotrione 12 70 A1 & Mesotrione 1 + 12 100 (E = 94) Δ = 6 0.0625 + 12 80 (E = 70) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 50 Metribuzin 15 10 A1 & Metribuzin 0.25 + 15 70 (E = 55) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Metribuzin 15 0 A1 & Metribuzin 0.0625 + 15 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 10 Oxadiazon 20 10 A1 & Oxadiazon 0.25 + 20 60 (E = 37) Δ = 23 0.0625 + 20 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Oxyfluorfen 3 20 1 10 A1 & Oxyfluorfen 0.25 + 3 50 (E = 44) Δ = 6 0.25 + 1 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 50 0.0625 10 Paraquat 120 40 A1 & Paraquat 0.25 + 120 93 (E = 70) Δ = 23 0.0625 + 120 93 (E = 46) Δ = 47 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Paraquat 120 50 A1 & Paraquat 0.0625 + 120 80 (E = 50) Δ = 30 BCS231024-Ausland STR 151 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 50 Pyroxasulfone 45 20 A1 & Pyroxasulfone 0.25 + 45 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Rimsulfuron 2.7 40 A1 & Rimsulfuron 0.0625 + 2.7 60 (E = 40) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 50 Saflufenacil 1.2 85 A1 & Saflufenacil 0.25 + 1.2 100 (E = 92.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Saflufenacil 1.2 50 A1 & Saflufenacil 0.0625 + 1.2 60 (E = 50) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 1 80 0.0625 10 S-Metolachlor 150 10 50 10 A1 & S-Metolachlor 1 + 150 30 (E = 19) Δ = 11 0.0625 + 150 99 (E = 82) Δ = 17 0.0625 + 50 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 1 80 0.0625 0 S-Metolachlor 150 0 50 0 A1 & S-Metolachlor 1 + 150 40 (E = 0) Δ = 40 0.0625 + 150 98 (E = 80) Δ = 18 0.0625 + 50 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Sulfentrazone 3 30 A1 & Sulfentrazone 0.25 + 3 60 (E = 51) Δ = 9 BCS231024-Ausland STR 152 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.25 20 Sulfentrazone 3 20 A1 & Sulfentrazone 0.25 + 3 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 0 Tembotrione 9 40 3 30 A1 & Tembotrione 0.25 + 9 80 (E = 58) Δ = 22 0.25 + 3 60 (E = 51) Δ = 9 0.0625 + 9 60 (E = 40) Δ = 20 0.0625 + 3 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.0625 0 Tembotrione 9 20 A1 & Tembotrione 0.0625 + 9 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 0.0625 10 Terbuthylanzine 150 50 50 20 A1 & Terbuthylanzine 0.25 + 150 60 (E = 55) Δ = 5 0.25 + 50 100 (E = 65) Δ = 35 0.0625 + 150 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.25 20 Terbuthylanzine 150 30 A1 & Terbuthylanzine 0.25 + 150 100 (E = 44) Δ = 56 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 10 DAT A1 0.25 30 Tiafenacil 0.33 30 A1 & Tiafenacil 0.25 + 0.33 99 (E = 51) Δ = 48 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 21 DAT A1 0.25 20 Tiafenacil 0.33 20 A1 & Tiafenacil 0.25 + 0.33 99 (E = 36) Δ = 63 BCS231024-Ausland STR 153 Active ingredient Application rate Herbicidal effect [%] against g ai / ha CENCY 10 DAT A1 1 80 0.25 50 0.0625 10 Trifludimoxazine 1.2 30 0.4 25 A1 & Trifludimoxazine 1 + 1.2 98 (E = 86) Δ = 12 0.25 + 1.2 85 (E = 65) Δ = 20 0.0625 + 1.2 90 (E = 37) Δ = 53 0.0625 + 0.4 40 (E = 32.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha CENCY 21 DAT A1 0.25 70 0.0625 0 Trifludimoxazine 1.2 20 0.4 30 A1 & Trifludimoxazine 0.25 + 1.2 80 (E = 30) Δ = 50 0.0625 + 1.2 98 (E = 76) Δ = 22 0.0625 + 0.4 80 (E = 20) Δ = 60 Table 3.7: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Echinochloa crus-galli (ECHCG) Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.0625 0 2,4-D 120 20 40 10 A1 & 2,4-D 1 + 120 30 (E = 20) Δ = 10 1 + 40 88 (E = 44) Δ = 44 0.0625 + 120 85 (E = 37) Δ = 48 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.25 10 0.0625 0 2,4-D 120 0 40 0 ​​A1 & 2,4-D 1 + 120 85 (E = 20) Δ = 65 1 + 40 75 (E = 20) Δ = 55 0.25 + 120 20 (E = 10) Δ = 10 0.0625 + 120 20 (E = 0) Δ = 20 BCS231024-Ausland STR 154 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 Aclonifen 90 10 A1 & Aclonifen 0.25 + 90 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.25 10 Aclonifen 90 10 A1 & Aclonifen 0.25 + 90 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 Atrazine 150 40 A1 & Atrazine 0.25 + 150 80 (E = 67) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 50 Atrazine 150 10 A1 & Atrazine 0.25 + 150 80 (E = 55) Δ = 25 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 70 0.25 30 0.0625 10 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.0625 20 carboxylate 0.25 40 A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6- dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 1 + 0.0625 60 (E = 46) Δ = 14 oxazole-5-carboxylate 0.25 + 0.25 85 (E = 76) Δ = 9 0.0625 + 0.25 85 (E = 58) Δ = 27 BCS231024-Ausland STR 155 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 40 0.25 20 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.25 40 carboxylate 0.0625 20 A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 1 + 0.25 80 (E = 52) Δ = 28 oxazole-5-carboxylate 1 + 0.0625 75 (E = 64) Δ = 11 0.25 + 0.25 85 (E = 52) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 40 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.5 60 5-carboxylic acid A1 & 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazol-1 + 0.5 85 (E = 76) Δ = 95-carboxylic acid Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 40 0.25 20 0.0625 10 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.25 60 yl]benzyliden}amino]oxy}propanoate 0.0625 40 A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)-1 + 0.25 85 (E = 76) Δ = 9yl]benzylidene}amino]oxy}propanoate 1 + 0.0625 80 (E = 64) Δ = 16 0.25 + 0.25 88 (E = 68) Δ = 20 0.0625 + 0.25 80 (E = 64) Δ = 16 BCS231024-Ausland STR 156 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.25 10 0.0625 0 Bicyclopyrone 9 60 3 40 A1 & Bicyclopyrone 1 + 9 96 (E = 72) Δ = 24 1 + 3 85 (E = 58) Δ = 27 0.25 + 9 88 (E = 64) Δ = 24 0.0625 + 9 90 (E = 60) Δ = 30 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 20 Bicyclopyrone 9 30 3 20 A1 & Bicyclopyrone 1 + 9 96 (E = 44) Δ = 52 1 + 3 60 (E = 36) Δ = 24 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.0625 0 Bromoxynil 80 0 A1 & Bromoxynil 0.0625 + 80 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 0.0625 10 Butafenacil 1 25 0.33 20 A1 & Butafenacil 0.25 + 1 50 (E = 40) Δ = 10 0.0625 + 0.33 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.25 10 0.0625 0 Clethodim 24 90 8 88 A1 & Clethodim 1 + 24 100 (E = 93) Δ = 7 1 + 8 97 (E = 91.6) Δ = 5.4 0.25 + 24 97 (E = 91) Δ = 6 0.0625 + 24 95 (E = 90) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.0625 0 Clethodim 24 95 A1 & Clethodim 0.0625 + 24 100 (E = 95) Δ = 5 BCS231024-Ausland STR 157 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.25 10 0.0625 0 Dicamba 15 0 5 0 A1 & Dicamba 1 + 15 40 (E = 30) Δ = 10 1 + 5 30 (E = 10) Δ = 20 0.25 + 15 20 (E = 10) Δ = 10 0.25 + 5 10 (E = 0) Δ = 10 0.0625 + 15 75 (E = 30) Δ = 45 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.25 10 Dicamba 15 0 5 0 A1 & Dicamba 1 + 15 20 (E = 10) Δ = 10 1 + 5 70 (E = 20) Δ = 50 0.25 + 15 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.25 10 Florpyrauxifen 3 20 1 10 A1 & Florpyrauxifen 1 + 3 40 (E = 28) Δ = 12 1 + 1 97 (E = 44) Δ = 53 0.25 + 3 80 (E = 37) Δ = 43 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 20 Florpyrauxifen 3 20 1 10 A1 & Florpyrauxifen 1 + 3 96 (E = 36) Δ = 60 1 + 1 70 (E = 28) Δ = 42 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 Flufenacet 45 40 A1 & Flufenacet 0.25 + 45 60 (E = 52) Δ = 8 BCS231024-Ausland STR 158 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 40 0.0625 10 Flufenoximacil 0.0625 70 A1 & Flufenoximacil 1 + 0.0625 100 (E = 82) Δ = 18 0.0625 + 0.0625 85 (E = 73) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Flumioxazin 1.2 70 0.4 30 A1 & Flumioxazin 0.25 + 1.2 98 (E = 83.5) Δ = 14.5 0.25 + 0.4 95 (E = 61.5) Δ = 33.5 0.0625 + 1.2 99 (E = 76) Δ = 23 0.0625 + 0.4 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 50 0.0625 0 Flumioxazin 1.2 20 0.4 10 A1 & Flumioxazin 0.25 + 1.2 85 (E = 60) Δ = 25 0.25 + 0.4 70 (E = 55) Δ = 15 0.0625 + 1.2 88 (E = 20) Δ = 68 0.0625 + 0.4 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Fomesafen 1.5 10 A1 & Fomesafen 0.25 + 1.5 70 (E = 50.5) Δ = 19.5 0.0625 + 1.5 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 80 0.25 50 0.0625 0 Fomesafen 1.5 0 A1 & Fomesafen 1 + 1.5 10 (E = 0) Δ = 10 0.25 + 1.5 88 (E = 80) Δ = 8 0.0625 + 1.5 70 (E = 50) Δ = 20 BCS231024-Ausland STR 159 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.0625 0 Glufosinate 90 70 A1 & Glufosinate 0.0625 + 90 80 (E = 70) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 10 0.0625 0 Glyphosate 90 60 A1 & Glyphosate 0.25 + 90 80 (E = 64) Δ = 16 0.0625 + 90 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.25 10 0.0625 0 Glyphosate 30 0 90 30 A1 & Glyphosate 1 + 30 40 (E = 20) Δ = 20 0.25 + 30 20 (E = 10) Δ = 10 0.0625 + 90 40 (E = 30) Δ = 10 0.0625 + 30 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 Imazethapyr 7.5 80 2.5 60 A1 & Imazethapyr 0.25 + 7.5 90 (E = 84) Δ = 6 0.25 + 2.5 80 (E = 68) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 10 0.0625 10 Imazethapyr 7.5 70 A1 & Imazethapyr 0.25 + 7.5 85 (E = 73) Δ = 12 0.0625 + 7.5 80 (E = 73) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 30 0.25 10 0.0625 0 Indaziflam 3 10 9 40 A1 & Indaziflam 1 + 3 50 (E = 40) Δ = 10 0.25 + 9 60 (E = 37) Δ = 23 0.0625 + 9 60 (E = 46) Δ = 14 BCS231024-Ausland STR 160 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.25 10 0.0625 0 Indaziflam 3 0 9 40 A1 & Indaziflam 1 + 3 40 (E = 20) Δ = 20 0.25 + 3 20 (E = 10) Δ = 10 0.0625 + 9 60 (E = 40) Δ = 20 0.0625 + 3 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.25 10 0.0625 0 Iodosulfuron 3 75 A1 & Iodosulfuron 1 + 3 80 (E = 75) Δ = 5 0.25 + 3 85 (E = 80) Δ = 5 0.0625 + 3 90 (E = 77.5) Δ = 12.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 1 30 Mesotrione 4 40 A1 & Mesotrione 1 + 4 75 (E = 58) Δ = 17 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 20 0.0625 0 Mesotrione 12 75 A1 & Mesotrione 1 + 12 85 (E = 80) Δ = 5 0.0625 + 12 80 (E = 75) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Metribuzin 45 20 15 10 A1 & Metribuzin 0.25 + 45 85 (E = 56) Δ = 29 0.25 + 15 75 (E = 50.5) Δ = 24.5 0.0625 + 45 80 (E = 36) Δ = 44 0.0625 + 15 50 (E = 28) Δ = 22 BCS231024-Ausland STR 161 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 1 80 0.25 50 0.0625 0 Metribuzin 45 0 A1 & Metribuzin 1 + 45 60 (E = 0) Δ = 60 0.25 + 45 85 (E = 80) Δ = 5 0.0625 + 45 83 (E = 50) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 Oxadiazon 60 40 A1 & Oxadiazon 0.25 + 60 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 10 Oxyfluorfen 3 10 1 10 A1 & Oxyfluorfen 0.25 + 3 30 (E = 19) Δ = 11 0.25 + 1 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.0625 0 Paraquat 120 80 40 50 A1 & Paraquat 0.0625 + 120 88 (E = 80) Δ = 8 0.0625 + 40 70 (E = 50) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Pendimethalin 300 75 100 60 A1 & Pendimethalin 0.25 + 300 95 (E = 86.25) Δ = 8.75 0.25 + 100 85 (E = 78) Δ = 7 0.0625 + 300 95 (E = 80) Δ = 15 0.0625 + 100 80 (E = 68) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.0625 0 Pendimethalin 300 85 100 60 A1 & Pendimethalin 0.0625 + 300 95 (E = 85) Δ = 10 0.0625 + 100 75 (E = 60) Δ = 15 BCS231024-Ausland STR 162 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 21 DAT A1 0.0625 0 Pyroxasulfone 15 80 A1 & Pyroxasulfone 0.0625 + 15 90 (E = 80) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Saflufenacil 1.2 40 0.4 10 A1 & Saflufenacil 0.25 + 1.2 85 (E = 67) Δ = 18 0.25 + 0.4 75 (E = 50.5) Δ = 24.5 0.0625 + 1.2 75 (E = 52) Δ = 23 0.0625 + 0.4 40 (E = 28) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 80 0.25 50 0.0625 0 Saflufenacil 1.2 10 0.4 0 A1 & Saflufenacil 1 + 1.2 88 (E = 82) Δ = 6 0.25 + 1.2 70 (E = 55) Δ = 15 0.25 + 0.4 60 (E = 50) Δ = 10 0.0625 + 1.2 30 (E = 10) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.0625 20 S-Metolachlor 50 75 A1 & S-Metolachlor 0.0625 + 50 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 80 0.0625 0 S-Metolachlor 50 75 A1 & S-Metolachlor 1 + 50 100 (E = 95) Δ = 5 0.0625 + 50 88 (E = 75) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 10 Sulfentrazone 1 10 A1 & Sulfentrazone 0.25 + 1 30 (E = 19) Δ = 11 BCS231024-Ausland STR 163 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 0.0625 10 Terbuthylanzine 150 25 50 10 A1 & Terbuthylanzine 0.25 + 150 50 (E = 40) Δ = 10 0.25 + 50 40 (E = 28) Δ = 12 0.0625 + 150 40 (E = 32.5) Δ = 7.5 0.0625 + 50 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.25 10 Terbuthylanzine 150 10 50 10 A1 & Terbuthylanzine 0.25 + 150 30 (E = 19) Δ = 11 0.25 + 50 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 20 Tiafenacil 0.33 30 A1 & Tiafenacil 0.25 + 0.33 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.25 45 0.0625 20 Trifludimoxazine 1.2 75 0.4 40 A1 & Trifludimoxazine 0.25 + 1.2 93 (E = 80) Δ = 13 0.25 + 0.4 98 (E = 86.25) Δ = 11.75 0.0625 + 1.2 80 (E = 67) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 1 80 0.25 50 0.0625 0 Trifludimoxazine 1.2 50 0.4 10 A1 & Trifludimoxazine 1 + 1.2 100 (E = 90) Δ = 10 1 + 0.4 100 (E = 82) Δ = 18 0.25 + 1.2 85 (E = 75) Δ = 10 0.0625 + 1.2 83 (E = 50) Δ = 33 BCS231024-Ausland STR 164 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 10 DAT A1 0.45 60 0.15 30 2-chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3- [(S)-methylsulfinyl]-4- 2 80 (trifluoromethyl)benzamide A1 + 2-chloro-N-(5-methyl-1,3,4-oxadiazol-2- yl)-3-[(S)-methylsulfinyl]-4- 0.45 + 2 96 (E = 92) Δ = 4 (trifluoromethyl)benzamide A1 + 2-chloro-N-(5-methyl-1,3,4-oxadiazol-2- yl)-3-[(S)-methylsulfinyl]-4- 0.15 + 2 95 (E = 86) Δ = 9 (trifluoromethyl)benzamide Active ingredient Application rate Herbicidal activity [%] against g ai / ha ECHCG 21 DAT A1 0.45 40 0.15 10 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3-[(S)-methylsulfinyl]-4- 2 90 (trifluoromethyl)benzamide A1 + 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2- yl)-3-[(S)-methylsulfinyl]-4- 0.45 + 2 99 (E = 94) Δ = 5 (trifluoromethyl)benzamide A1 + 2-chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3-[(S)-methylsulfinyl]-4- 0.15 + 2 97 (E = 91) Δ = 6 (trifluoromethyl)benzamide tables 3.8: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Eleusine indica (ELEIN) Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 80 0.0625 0 2,4-D 120 30 A1 & 2,4-D 1 + 120 95 (E = 86) Δ = 9 0.0625 + 120 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 2,4-D 120 10 40 0 ​​A1 & 2,4-D 0.0625 + 120 30 (E = 10) Δ = 20 0.0625 + 40 10 (E = 0) Δ = 10 BCS231024-Ausland STR 165 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 Aclonifen 90 20 A1 & Aclonifen 0.25 + 90 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 0.0625 20 Atrazine 50 10 150 30 A1 & Atrazine 1 + 50 95 (E = 65) Δ = 30 0.25 + 150 60 (E = 55) Δ = 5 0.25 + 50 50 (E = 44) Δ = 6 0.0625 + 150 40 (E = 28) Δ = 12 0.0625 + 50 93 (E = 77.5) Δ = 15.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 Atrazine 150 50 A1 & Atrazine 0.25 + 150 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.0625 20 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate 0.0625 40 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 0.0625 + 0.0625 70 (E = 52 Δ) = 18 oxazole-5-carboxylate Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 0.0625 20 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.25 88 yl]benzyliden}amino]oxy}propanoate0.0625 50 A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)-0.25 + 0.25 100 (E = 95.2 Δ) = 4.8yl]benzylidene}amino]oxy}propanoate 0.25 + 0.0625 88 (E = 80) Δ = 8 0.0625 + 0.25 100 (E = 90.4) Δ = 9.6 0.0625 + 0.0625 80 (E = 60) Δ = 20 BCS231024-Ausland STR 166 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Bicyclopyrone 9 80 A1 & Bicyclopyrone 0.0625 + 9 97 (E = 80) Δ = 17 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 Bromoxynil 240 20 A1 & Bromoxynil 1 + 240 99 (E = 80) Δ = 19 0.25 + 240 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 1 80 0.25 60 0.0625 0 Bromoxynil 240 0 80 0 A1 & Bromoxynil 1 + 240 20 (E = 0) Δ = 20 0.25 + 240 93 (E = 80) Δ = 13 0.0625 + 80 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Butafenacil 1 50 A1 & Butafenacil 0.25 + 1 93 (E = 65) Δ = 28 0.0625 + 1 75 (E = 55) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 1 85 0.25 20 Butafenacil 1 20 A1 & Butafenacil 1 + 1 95 (E = 88) Δ = 7 0.25 + 1 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 80 0.25 20 0.0625 0 Clethodim 8 20 24 70 A1 & Clethodim 1 + 8 85 (E = 76) Δ = 9 0.25 + 24 85 (E = 36) Δ = 49 0.25 + 8 85 (E = 70) Δ = 15 0.0625 + 24 85 (E = 20) Δ = 65 0.0625 + 8 90 (E = 84) Δ = 6 BCS231024-Ausland STR 167 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Clethodim 24 60 A1 & Clethodim 0.0625 + 24 80 (E = 60) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 80 0.0625 0 Dicamba 15 0 5 0 A1 & Dicamba 1 + 15 10 (E = 0) Δ = 10 1 + 5 85 (E = 80) Δ = 5 0.0625 + 15 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.25 20 Dicamba 15 0 A1 & Dicamba 0.25 + 15 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 Diuron 120 40 A1 & Diuron 0.25 + 120 70 (E = 58) Δ = 12 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 1 85 Diuron 120 20 40 10 A1 & Diuron 1 + 120 98 (E = 88) Δ = 10 1 + 40 95 (E = 86.5) Δ = 8.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 1 80 0.25 20 Florpyrauxifen 3 0 1 0 A1 & Florpyrauxifen 1 + 3 30 (E = 20) Δ = 10 1 + 1 88 (E = 80) Δ = 8 0.25 + 1 88 (E = 80) Δ = 8 BCS231024-Ausland STR 168 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 1 80 Florpyrauxifen 3 0 1 0 A1 & Florpyrauxifen 1 + 3 85 (E = 80) Δ = 5 1 + 1 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 1 85 Flufenacet 45 30 15 10 A1 & Flufenacet 1 + 45 95 (E = 89.5) Δ = 5.5 1 + 15 97 (E = 86.5) Δ = 10.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.0625 20 Flumioxazin 1.2 50 A1 & Flumioxazin 0.0625 + 1.2 80 (E = 60) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Flumioxazin 1.2 60 0.4 40 A1 & Flumioxazin 0.0625 + 1.2 80 (E = 60) Δ = 20 0.0625 + 0.4 60 (E = 40) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Fluometuron 300 60 100 20 A1 & Fluometuron 0.25 + 300 80 (E = 72) Δ = 8 0.25 + 100 80 (E = 44) Δ = 36 0.0625 + 300 75 (E = 64) Δ = 11 0.0625 + 100 75 (E = 28) Δ = 47 BCS231024-Ausland STR 169 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 1 85 0.25 20 0.0625 10 Fluometuron 100 10 300 20 A1 & Fluometuron 1 + 100 50 (E = 36) Δ = 14 0.25 + 300 50 (E = 28) Δ = 22 0.25 + 100 40 (E = 28) Δ = 12 0.0625 + 300 40 (E = 19) Δ = 21 0.0625 + 100 93 (E = 86.5) Δ = 6.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 0.0625 20 Fomesafen 4.5 30 1.5 10 A1 & Fomesafen 1 + 4.5 98 (E = 82.5) Δ = 15.5 0.25 + 4.5 70 (E = 65) Δ = 5 0.25 + 1.5 70 (E = 55) Δ = 15 0.0625 + 4.5 60 (E = 44) Δ = 16 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 0.0625 0 Fomesafen 1.5 0 4.5 0 A1 & Fomesafen 0.25 + 1.5 70 (E = 60) Δ = 10 0.0625 + 4.5 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Foramsulfuron 3 85 A1 & Foramsulfuron 0.0625 + 3 90 (E = 85) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 20 0.0625 0 Glyphosate 90 60 30 20 A1 & Glyphosate 0.25 + 90 80 (E = 60) Δ = 20 0.25 + 30 80 (E = 68) Δ = 12 0.0625 + 90 60 (E = 36) Δ = 24 BCS231024-Ausland STR 170 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 20 0.0625 0 Glyphosate 90 0 A1 & Glyphosate 0.25 + 90 30 (E = 20) Δ = 10 0.0625 + 90 30 (E = 0) Δ = 30 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.25 50 Icafolin-methyl 1.2 20 A1 & Icafolin-methyl 0.25 + 1.2 70 (E = 60) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Imazethapyr 2.5 10 A1 & Imazethapyr 0.25 + 2.5 50 (E = 37) Δ = 13 0.0625 + 2.5 40 (E = 19) Δ = 21 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 20 0.0625 0 Indaziflam 9 0 3 0 A1 & Indaziflam 0.25 + 9 30 (E = 20) Δ = 10 0.25 + 3 80 (E = 20) Δ = 60 0.0625 + 9 10 (E = 0) Δ = 10 0.0625 + 3 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 20 Indaziflam 3 10 A1 & Indaziflam 0.25 + 3 75 (E = 28) Δ = 47 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 1 80 0.25 20 Iodosulfuron 3 10 1 0 A1 & Iodosulfuron 1 + 3 50 (E = 28) Δ = 22 1 + 1 88 (E = 82) Δ = 6 0.25 + 3 85 (E = 80) Δ = 5 BCS231024-Ausland STR 171 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Isoxaflutole 12 88 A1 & Isoxaflutole 0.0625 + 12 95 (E = 88) Δ = 7 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Mesosulfuron-Methyl 1.2 3 0.4 0 A1 & Mesosulfuron-Methyl 0.25 + 1.2 98 (E = 32.1) Δ = 65.9 0.25 + 0.4 60 (E = 30) Δ = 30 0.0625 + 1.2 50 (E = 12.7) Δ = 37.3 0.0625 + 0.4 30 (E = 10) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 0.0625 20 Metribuzin 45 70 A1 & Metribuzin 1 + 45 98 (E = 76) Δ = 22 0.25 + 45 99 (E = 92.5) Δ = 6.5 0.0625 + 45 99 (E = 85) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 Metribuzin 45 80 A1 & Metribuzin 0.25 + 45 98 (E = 92) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Oxadiazon 60 70 20 50 A1 & Oxadiazon 0.25 + 60 93 (E = 79) Δ = 14 0.25 + 20 70 (E = 65) Δ = 5 0.0625 + 60 90 (E = 73) Δ = 17 0.0625 + 20 60 (E = 55) Δ = 5 BCS231024-Ausland STR 172 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 1 85 0.25 20 0.0625 10 Oxadiazon 60 30 20 10 A1 & Oxadiazon 1 + 60 100 (E = 86.5) Δ = 13.5 1 + 20 70 (E = 44) Δ = 26 0.25 + 60 35 (E = 28) Δ = 7 0.25 + 20 60 (E = 37) Δ = 23 0.0625 + 60 100 (E = 89.5) Δ = 10.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Oxyfluorfen 3 40 1 30 A1 & Oxyfluorfen 0.25 + 3 75 (E = 58) Δ = 17 0.25 + 1 60 (E = 51) Δ = 9 0.0625 + 3 60 (E = 46) Δ = 14 0.0625 + 1 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 50 Paraquat 40 70 A1 & Paraquat 0.25 + 40 93 (E = 85) Δ = 8 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 Pendimethalin 100 0 A1 & Pendimethalin 0.25 + 100 80 (E = 60) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 Pyraflufen-ethyl 30 75 A1 & Pyraflufen-ethyl 1 + 30 99 (E = 93.75) Δ = 5.25 0.25 + 30 98 (E = 87.5) Δ = 10.5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 Pyraflufen-ethyl 30 70 A1 & Pyraflufen-ethyl 0.25 + 30 93 (E = 88) Δ = 5 BCS231024-Ausland STR 173 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Rimsulfuron 2.7 70 A1 & Rimsulfuron 0.0625 + 2.7 80 (E = 70) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 1 75 0.25 50 0.0625 20 Saflufenacil 1.2 20 0.4 10 A1 & Saflufenacil 1 + 1.2 93 (E = 80) Δ = 13 0.25 + 1.2 85 (E = 60) Δ = 25 0.25 + 0.4 75 (E = 55) Δ = 20 0.0625 + 0.4 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.25 60 0.0625 0 Saflufenacil 0.4 0 A1 & Saflufenacil 0.25 + 0.4 70 (E = 60) Δ = 10 0.0625 + 0.4 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g a.i. / ha ELEIN 10 DAT A1 0.0625 10 Sulfentrazone 1 10 A1 & Sulfentrazone 0.0625 + 1 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Terbuthylanzine 50 40 A1 & Terbuthylanzine 0.25 + 50 75 (E = 58) Δ = 17 0.0625 + 50 60 (E = 46) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 1 85 0.0625 10 Terbuthylanzine 150 50 50 10 A1 & Terbuthylanzine 1 + 150 98 (E = 92.5) Δ = 5.5 0.0625 + 50 30 (E = 19) Δ = 11 BCS231024-Ausland STR 174 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.0625 0 Thiencarbazone 0.33 75 A1 & Thiencarbazone 0.0625 + 0.33 80 (E = 75) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Thiencarbazone 0.33 20 A1 & Thiencarbazone 0.0625 + 0.33 30 (E = 20) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha ELEIN 10 DAT A1 0.25 30 0.0625 10 Tiafenacil 1 60 0.33 50 A1 & Tiafenacil 0.25 + 1 93 (E = 64) Δ = 29 0.25 + 0.33 98 (E = 72) Δ = 26 0.0625 + 1 75 (E = 65) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.25 20 0.0625 10 Tiafenacil 1 30 0.33 20 A1 & Tiafenacil 0.25 + 1 50 (E = 37) Δ = 13 0.25 + 0.33 93 (E = 44) Δ = 49 0.0625 + 1 50 (E = 36) Δ = 14 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 10 DAT A1 0.25 50 0.0625 20 Trifludimoxazine 0.4 40 1.2 60 A1 & Trifludimoxazine 0.25 + 0.4 75 (E = 70) Δ = 5 0.0625 + 1.2 98 (E = 68) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha ELEIN 21 DAT A1 0.0625 0 Trifludimoxazine 1.2 70 A1 & Trifludimoxazine 0.0625 + 1.2 80 (E = 70) Δ = 10 BCS231024-Ausland STR 175 Tables 3.9: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Kochia scoparia (KCHSC) Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Acetochlor 150 0 450 0 A1 & Acetochlor 0.25 + 150 20 (E = 0) Δ = 20 0.0625 + 450 80 (E = 70) Δ = 10 0.0625 + 150 30 (E = 0) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Aclonifen 30 30 A1 & Aclonifen 0.25 + 30 70 (E = 65) Δ = 5 0.0625 + 30 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 Aclonifen 90 50 A1 & Aclonifen 0.25 + 90 70 (E = 65) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 30 Atrazine 50 70 A1 & Atrazine 0.0625 + 50 85 (E = 79) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Atrazine 150 70 A1 & Atrazine 0.25 + 150 99 (E = 91) Δ = 8 0.0625 + 150 80 (E = 70) Δ = 10 BCS231024-Ausland STR 176 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 1 40 0.25 20 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.25 75 carboxylate 0.0625 20 A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 1 + 0.25 90 (E = 36) Δ = 54 oxazole-5-carboxylate1 + 0.0625 90 (E = 85) Δ = 5 0.25 + 0.0625 98 (E = 52) Δ = 46 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 20 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole- 0.5 80 5-carboxylic acid A1 & 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-0.0625 + 0.5 97 (E = 84) Δ = 135-carboxylic acidActive ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 1 40 0.25 20 0.0625 10 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazol- 0.5 30 5-carboxylic acid 0.125 20 A1 &3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-1 + 0.5 99 (E = 52) Δ = 47 5-carboxylic acid 1 + 0.125 75 (E = 44) Δ = 31 0.25 + 0.5 75 (E = 36) Δ = 39 0.25 + 0.125 85 (E = 37) Δ = 48 0.0625 + 0.5 97 (E = 58) Δ = 39 BCS231024-Ausland STR 177 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Butafenacil 0.33 60 1 85 A1 & Butafenacil 0.25 + 0.33 70 (E = 64) Δ = 6 0.0625 + 1 85 (E = 80) Δ = 5 0.0625 + 0.33 93 (E = 86.5) Δ = 6.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 70 Clethodim 24 0 A1 & Clethodim 0.25 + 24 75 (E = 70) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 Clethodim 24 0 A1 & Clethodim 0.25 + 24 50 (E = 30) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 1 88 0.25 70 0.0625 0 Dicamba 15 30 5 20 A1 & Dicamba 1 + 15 95 (E = 79) Δ = 16 1 + 5 95 (E = 76) Δ = 19 0.25 + 15 60 (E = 30) Δ = 30 0.25 + 5 30 (E = 20) Δ = 10 0.0625 + 15 97 (E = 91.6) Δ = 5.4 0.0625 + 5 95 (E = 90.4) Δ = 4.6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 1 85 0.25 30 0.0625 0 Dicamba 15 0 5 0 A1 & Dicamba 1 + 15 88 (E = 30) Δ = 58 0.25 + 15 88 (E = 30) Δ = 58 0.25 + 5 30 (E = 0) Δ = 30 0.0625 + 15 40 (E = 0) Δ = 40 0.0625 + 5 95 (E = 85) Δ = 10 BCS231024-Ausland STR 178 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 Dimethenamid 120 20 40 10 A1 & Dimethenamid 0.25 + 120 75 (E = 60) Δ = 15 0.25 + 40 80 (E = 55) Δ = 25 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 Dimethenamid 120 10 40 10 A1 & Dimethenamid 0.25 + 120 60 (E = 37) Δ = 23 0.25 + 40 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.0625 0 Florpyrauxifen 3 75 A1 & Florpyrauxifen 0.0625 + 3 80 (E = 75) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Flufenacet 45 20 15 10 A1 & Flufenacet 0.25 + 45 50 (E = 19) Δ = 31 0.25 + 15 70 (E = 60) Δ = 10 0.0625 + 15 70 (E = 55) Δ = 15 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 Flufenacet 45 10 15 10 A1 & Flufenacet 0.25 + 45 50 (E = 37) Δ = 13 0.25 + 15 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 85 0.0625 30 Fomesafen 4.5 50 1.5 50 A1 & Fomesafen 0.25 + 4.5 80 (E = 65) Δ = 15 0.0625 + 4.5 98 (E = 92.5) Δ = 5.5 0.0625 + 1.5 98 (E = 65) Δ = 33 BCS231024-Ausland STR 179 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.0625 0 Fomesafen 4.5 50 1.5 70 A1 & Fomesafen 0.0625 + 4.5 98 (E = 50) Δ = 48 0.0625 + 1.5 80 (E = 70) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 0 Foramsulfuron 3 90 A1 & Foramsulfuron 0.0625 + 3 95 (E = 90) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.0625 0 Foramsulfuron 3 90 A1 & Foramsulfuron 0.0625 + 3 95 (E = 90) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 1 88 0.25 70 0.0625 0 Glufosinate 90 40 A1 & Glufosinate 1 + 90 70 (E = 40) Δ = 30 0.25 + 90 98 (E = 92.8) Δ = 5.2 0.0625 + 90 88 (E = 82) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 0 Glufosinate 90 20 30 20 A1 & Glufosinate 0.25 + 90 60 (E = 20) Δ = 40 0.25 + 30 75 (E = 44) Δ = 31 0.0625 + 90 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 0 Glyphosate 90 0 30 0 A1 & Glyphosate 0.0625 + 90 20 (E = 0) Δ = 20 0.0625 + 30 10 (E = 0) Δ = 10 BCS231024-Ausland STR 180 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.0625 0 Glyphosate 90 0 30 0 A1 & Glyphosate 0.0625 + 90 10 (E = 0) Δ = 10 0.0625 + 30 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.25 85 0.0625 30 Icafolin-methyl 1.2 10 A1 & Icafolin-methyl 0.25 + 1.2 93 (E = 86.5) Δ = 6.5 0.0625 + 1.2 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Icafolin-methyl 1.2 0 A1 & Icafolin-methyl 0.25 + 1.2 85 (E = 70) Δ = 15 0.0625 + 1.2 50 (E = 0) Δ = 50 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 10 Imazethapyr 2.5 85 A1 & Imazethapyr 0.0625 + 2.5 93 (E = 86.5) Δ = 6.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 0 Indaziflam 9 30 3 30 A1 & Indaziflam 0.0625 + 9 60 (E = 30) Δ = 30 0.0625 + 3 60 (E = 30) Δ = 30 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 0 Indaziflam 9 30 3 40 A1 & Indaziflam 0.25 + 9 60 (E = 30) Δ = 30 0.25 + 3 80 (E = 51) Δ = 29 0.0625 + 9 85 (E = 58) Δ = 27 BCS231024-Ausland STR 181 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Mesosulfuron-Methyl 1.2 70 A1 & Mesosulfuron-Methyl 0.25 + 1.2 90 (E = 85) Δ = 5 0.0625 + 1.2 80 (E = 73) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 Mesosulfuron-Methyl 1.2 50 0.4 10 A1 & Mesosulfuron-Methyl 0.25 + 1.2 75 (E = 65) Δ = 10 0.25 + 0.4 50 (E = 37) Δ = 13 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 30 Metribuzin 15 85 A1 & Metribuzin 0.0625 + 15 99 (E = 89.5) Δ = 9.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Oxadiazon 20 70 60 90 A1 & Oxadiazon 0.25 + 20 97 (E = 73) Δ = 24 0.0625 + 60 98 (E = 85) Δ = 13 0.0625 + 20 98 (E = 91) Δ = 7 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 10 Oxadiazon 60 70 20 60 A1 & Oxadiazon 0.25 + 60 96 (E = 79) Δ = 17 0.25 + 20 98 (E = 72) Δ = 26 0.0625 + 60 95 (E = 73) Δ = 22 0.0625 + 20 93 (E = 64) Δ = 29 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Oxyfluorfen 1 50 A1 & Oxyfluorfen 0.25 + 1 90 (E = 75) Δ = 15 0.0625 + 1 70 (E = 55) Δ = 15 BCS231024-Ausland STR 182 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 10 Oxyfluorfen 3 30 1 10 A1 & Oxyfluorfen 0.25 + 3 90 (E = 51) Δ = 39 0.25 + 1 70 (E = 37) Δ = 33 0.0625 + 3 70 (E = 37) Δ = 33 0.0625 + 1 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.0625 30 Paraquat 40 90 A1 & Paraquat 0.0625 + 40 98 (E = 93) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.0625 0 Paraquat 120 95 A1 & Paraquat 0.0625 + 120 100 (E = 95) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 85 Pendimethalin 300 30 A1 & Pendimethalin 0.25 + 300 97 (E = 89.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Pendimethalin 300 0 A1 & Pendimethalin 0.25 + 300 93 (E = 70) Δ = 23 0.0625 + 300 70 (E = 0) Δ = 70 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Pyroxasulfone 45 0 A1 & Pyroxasulfone 0.25 + 45 85 (E = 70) Δ = 15 0.0625 + 45 40 (E = 0) Δ = 40 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 10 DAT A1 0.0625 30 Saflufenacil 1.2 85 A1 & Saflufenacil 0.0625 + 1.2 99 (E = 89.5) Δ = 9.5 BCS231024-Ausland STR 183 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Saflufenacil 0.4 80 1.2 90 A1 & Saflufenacil 0.25 + 0.4 100 (E = 94) Δ = 6 0.0625 + 1.2 97 (E = 90) Δ = 7 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 S-Metolachlor 50 0 150 0 A1 & S-Metolachlor 0.25 + 50 30 (E = 0) Δ = 30 0.0625 + 150 80 (E = 70) Δ = 10 0.0625 + 50 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Sulfentrazone 1 85 A1 & Sulfentrazone 0.25 + 1 99 (E = 92.5) Δ = 6.5 0.0625 + 1 98 (E = 86.5) Δ = 11.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 10 Sulfentrazone 1 85 A1 & Sulfentrazone 0.25 + 1 98 (E = 89.5) Δ = 8.5 0.0625 + 1 97 (E = 86.5) Δ = 10.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.25 50 0.0625 10 Tiafenacil 0.33 50 A1 & Tiafenacil 0.25 + 0.33 90 (E = 75) Δ = 15 0.0625 + 0.33 75 (E = 55) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 30 0.0625 10 Tiafenacil 1 80 0.33 20 A1 & Tiafenacil 0.25 + 1 97 (E = 86) Δ = 11 0.25 + 0.33 75 (E = 44) Δ = 31 0.0625 + 1 99 (E = 82) Δ = 17 0.0625 + 0.33 50 (E = 28) Δ = 22 BCS231024-Ausland STR 184 Active ingredient Application rate Herbicidal effect [%] against g ai / ha KCHSC 21 DAT A1 0.25 70 0.0625 0 Trifludimoxazine 0.4 80 A1 & Trifludimoxazine 0.25 + 0.4 99 (E = 94) Δ = 5 0.0625 + 0.4 85 (E = 80) Δ = 5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha KCHSC 10 DAT A1 0.15 20 2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)- 3-[(S)-methylsulfinyl]-4- 2 50 (trifluoromethyl)benzamide A. 1 +2-Chloro-N-(5-methyl-1,3,4-oxadiazol-2-yl)-3-[(S)-methylsulfinyl]-4- 0.15 + 2 90 (E = 60) Δ = 30 (trifluoromethyl)benzamide Table 3.10: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Lolium rigidum (LOLRI) Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 0.25 0 2,4-D 40 0 ​​A1 & 2,4-D 0.25 + 40 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 10 0.25 10 Acetochlor 150 20 A1 & Acetochlor 1 + 150 55 (E = 28) Δ = 27 0.25 + 150 50 (E = 28) Δ = 22 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 0 0.25 0 Acetochlor 150 0 A1 & Acetochlor 1 + 150 20 (E = 0) Δ = 20 0.25 + 150 30 (E = 0) Δ = 30 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 0.25 10 Aclonifen 90 10 A1 & Aclonifen 0.25 + 90 30 (E = 19) Δ = 11 BCS231024-Ausland STR 185 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 20 0.0625 0 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazol-5- 0.0625 10 carboxylate 0.25 20 A1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 1 + 0.0625 50 (E = 37) Δ = 13 oxazole-5-carboxylate 0.25 + 0.25 60 (E = 36) Δ = 24 0.0625 + 0.25 60 (E = 20) Δ = 40 0.0625 + 0.0625 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 30 0.25 30 0.0625 20 Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.0625 0 c. arboxylatA1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 1 + 0.0625 30 (E = 20) Δ = 10 oxazole-5-carboxylate 0.25 + 0.0625 40 (E = 30) Δ = 10 0.0625 + 0.0625 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazol- 0.5 20 5-carboxylic acid A1 & 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4- sulfanyliden-1,3,5-triazinan-1-yl)-4- fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazol-1 + 0.5 60 (E = 44) Δ = 165-carboxylic acid BCS231024-Ausland STR 186 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- 0.0625 30 yl]benzylidene}amino]oxy}propanoate A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5- [3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- 1 + 0.0625 75 (E = 51) Δ = 24 yl]benzylidene}amino]oxy}propanoate Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 21 DAT A1 1 30 0.25 30 Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 0.25 50 yl]benzylidene}amino]oxy}propanoate 0.0625 30 A1 & Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- 1 + 0.25 70 (E = 65) Δ = 5yl]benzylidene}amino]oxy}propanoate 1 + 0.0625 75 (E = 65) Δ = 10 0.25 + 0.25 80 (E = 51) Δ = 29 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 0 Bromoxynil 240 0 A1 & Bromoxynil 1 + 240 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 10 0.0625 10 Butafenacil 1 30 0.33 10 A1 & Butafenacil 1 + 1 60 (E = 37) Δ = 23 1 + 0.33 50 (E = 37) Δ = 13 0.25 + 1 30 (E = 19) Δ = 11 0.25 + 0.33 40 (E = 19) Δ = 21 0.0625 + 0.33 70 (E = 51) Δ = 19 BCS231024-Ausland STR 187 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 10 0.0625 10 Dimethenamid 120 50 40 20 A1 & Dimethenamid 1 + 120 75 (E = 65) Δ = 10 1 + 40 50 (E = 44) Δ = 6 0.25 + 120 70 (E = 55) Δ = 15 0.0625 + 120 60 (E = 55) Δ = 5 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 0.25 10 Diuron 120 10 A1 & Diuron 0.25 + 120 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 Flufenacet 45 40 15 20 A1 & Flufenacet 1 + 45 80 (E = 58) Δ = 22 1 + 15 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 20 Flufenacet 45 30 A1 & Flufenacet 1 + 45 50 (E = 44) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 20 Flufenoximacil 0.0625 40 A1 & Flufenoximacil 1 + 0.0625 80 (E = 58) Δ = 22 0.25 + 0.0625 60 (E = 52) Δ = 8 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 21 DAT A1 1 30 Flufenoximacil 0.0625 40 A1 & Flufenoximacil 1 + 0.0625 70 (E = 58) Δ = 12 BCS231024-Ausland STR 188 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 10 0.25 10 Flumioxazin 1.2 10 0.4 10 A1 & Flumioxazin 1 + 1.2 30 (E = 19) Δ = 11 1 + 0.4 50 (E = 19) Δ = 31 0.25 + 1.2 35 (E = 19) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 0 Flumioxazin 0.4 0 A1 & Flumioxazin 1 + 0.4 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 Fluometuron 300 35 A1 & Fluometuron 1 + 300 60 (E = 54.5) Δ = 5.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 20 0.25 10 0.0625 0 Glyphosate 90 30 A1 & Glyphosate 1 + 90 75 (E = 30) Δ = 45 0.25 + 90 88 (E = 44) Δ = 44 0.0625 + 90 75 (E = 37) Δ = 38 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 10 0.25 0 0.0625 0 Glyphosate 90 0 A1 & Glyphosate 1 + 90 30 (E = 0) Δ = 30 0.25 + 90 30 (E = 10) Δ = 20 0.0625 + 90 20 (E = 0) Δ = 20 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 10 Icafolin-methyl 1.2 50 A1 & Icafolin-methyl 1 + 1.2 75 (E = 55) Δ = 20 BCS231024-Ausland STR 189 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 21 DAT A1 1 0 Icafolin-methyl 1,2 30 A1 & Icafolin-methyl 1 + 1,2 40 (E = 30) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 0,25 10 Imazethapyr 7,5 10 A1 & Imazethapyr 1 + 7,5 50 (E = 37) Δ = 13 0,25 + 7,5 30 (E = 19) Δ = 11 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 10 0,25 0 Isoxaflutole 12 0 A1 & Isoxaflutole 1 + 12 20 (E = 10) Δ = 10 0.25 + 12 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 21 DAT A1 1 10 0.25 0 Mesotrione 12 0 A1 & Mesotrione 1 + 12 20 (E = 10) Δ = 10 0.25 + 12 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 Oxadiazon 60 30 A1 & Oxadiazon 1 + 60 60 (E = 51) Δ = 9 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 10 0.0625 10 Oxyfluorfen 3 20 1 20 A1 & Oxyfluorfen 1 + 3 50 (E = 44) Δ = 6 1 + 1 50 (E = 44) Δ = 6 0.25 + 1 40 (E = 28) Δ = 12 0.0625 + 1 40 (E = 28) Δ = 12 BCS231024-Ausland STR 190 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 0.25 0 Paraquat 120 70 A1 & Paraquat 0.25 + 120 80 (E = 70) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 10 0.25 10 0.0625 10 Pyraflufen-ethyl 30 30 10 10 A1 & Pyraflufen-ethyl 1 + 30 40 (E = 19) Δ = 21 1 + 10 50 (E = 37) Δ = 13 0.25 + 30 30 (E = 19) Δ = 11 0.25 + 10 30 (E = 19) Δ = 11 0.0625 + 10 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 0 Pyraflufen-ethyl 30 10 A1 & Pyraflufen-ethyl 1 + 30 20 (E = 10) Δ = 10 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 21 DAT A1 1 0 0.25 0 Pyroxasulfone 45 80 A1 & Pyroxasulfone 1 + 45 85 (E = 80) Δ = 5 0.25 + 45 97 (E = 80) Δ = 17 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 10 Saflufenacil 1.2 10 A1 & Saflufenacil 1 + 1.2 25 (E = 19) Δ = 6 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 0.0625 10 S-Metolachlor 150 20 A1 & S-Metolachlor 0.0625 + 150 35 (E = 28) Δ = 7 BCS231024-Ausland STR 191 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 21 DAT A1 1 10 0.25 0 Tembotrione 9 0 3 0 A1 & Tembotrione 1 + 9 20 (E = 10) Δ = 10 1 + 3 20 (E = 10) Δ = 10 0.25 + 9 20 (E = 0) Δ = 20 0.25 + 3 10 (E = 0) Δ = 10 Active ingredient Application rate Herbicidal effect [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 10 Terbuthylanzine 150 20 50 10 A1 & Terbuthylanzine 1 + 150 30 (E = 19) Δ = 11 1 + 50 50 (E = 44) Δ = 6 0.25 + 50 70 (E = 37) Δ = 33 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 30 0.25 10 0.0625 10 Tiafenacil 0.33 10 A1 & Tiafenacil 1 + 0.33 30 (E = 19) Δ = 11 0.25 + 0.33 50 (E = 37) Δ = 13 0.0625 + 0.33 35 (E = 19) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha LOLRI 10 DAT A1 1 10 0.25 10 0.0625 10 Trifludimoxazine 1.2 10 0.4 10 A1 & Trifludimoxazine 1 + 1.2 40 (E = 19) Δ = 21 1 + 0.4 30 (E = 19) Δ = 11 0.25 + 1.2 40 (E = 19) Δ = 21 0.0625 + 1.2 30 (E = 19) Δ = 11 BCS231024-Ausland STR 192 Tables 3.11: Synergistic effect ∆t) ( for herbicidal binary compositions in Naclahua fuf when applied to Pharbitis purpurea (PHBPU) Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 0.0625 50 Acetochlor 450 10 A1 & Acetochlor 1 + 450 98 (E = 86.5) Δ = 11.5 0.0625 + 450 95 (E = 55) Δ = 40 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 0.0625 0 Acetochlor 150 0 A1 & Acetochlor 0.0625 + 150 30 (E = 0) Δ = 30 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 0.25 30 Aclonifen 90 20 30 10 A1 & Aclonifen 1 + 90 99 (E = 88) Δ = 11 1 + 30 99 (E = 86.5) Δ = 12.5 0.25 + 90 50 (E = 44) Δ = 6 0.25 + 30 60 (E = 37) Δ = 23 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 1 70 Aclonifen 90 10 30 10 A1 & Aclonifen 1 + 90 100 (E = 73) Δ = 27 1 + 30 100 (E = 73) Δ = 27 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 Atrazine 50 20 A1 & Atrazine 1 + 50 99 (E = 88) Δ = 11 BCS231024-Ausland STR 193 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 1 80 0.25 50 0.0625 0 Atrazine 50 0 150 0 A1 & Atrazine 1 + 50 60 (E = 50) Δ = 10 0.25 + 150 70 (E = 50) Δ = 20 0.25 + 50 20 (E = 0) Δ = 20 0.0625 + 150 10 (E = 0) Δ = 10 0.0625 + 50 98 (E = 80) Δ = 18 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 0.25 30 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5- 0.0625 88 c. arboxylatA1 & Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 0.25 + 0.0625 100 (E = 91.6 Δ) = 8.4 oxazole-5-carboxylate Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 21 DAT A1 0.25 20 Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo- 4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazol-5- 0.0625 88 carboxylate A1 & Ethyl 3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin- 1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2- 0.25 + 0.0625 100 (E = 90.4 Δ) = 9.6 oxazole-5-carboxylate Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 21 DAT A1 1 40 0.25 20 0.0625 0 Bicyclopyrone 9 30 A1 & Bicyclopyrone 1 + 9 95 (E = 30) Δ = 65 0.25 + 9 90 (E = 58) Δ = 32 0.0625 + 9 70 (E = 44) Δ = 26 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 Bromoxynil 240 50 A1 & Bromoxynil 1 + 240 99 (E = 92.5) Δ = 6.5 BCS231024-Ausland STR 194 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 1 80 Bromoxynil 240 60 A1 & Bromoxynil 1 + 240 98 (E = 92) Δ = 6 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 0.25 30 0.0625 10 Butafenacil 1 50 0.33 20 A1 & Butafenacil 1 + 1 70 (E = 65) Δ = 5 1 + 0.33 60 (E = 44) Δ = 16 0.25 + 1 85 (E = 55) Δ = 30 0.25 + 0.33 40 (E = 28) Δ = 12 0.0625 + 1 99 (E = 92.5) Δ = 6.5 0.0625 + 0.33 100 (E = 88) Δ = 12 Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 21 DAT A1 1 70 0.0625 10 Butafenacil 1 35 0.33 30 A1 & Butafenacil 1 + 1 80 (E = 41.5) Δ = 38.5 1 + 0.33 100 (E = 80.5) Δ = 19.5 0.0625 + 1 100 (E = 79) Δ = 21 Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 10 DAT A1 0.25 40 0.0625 10 Clethodim 24 0 8 0 A1 & Clethodim 0.25 + 24 30 (E = 10) Δ = 20 0.25 + 8 80 (E = 40) Δ = 40 0.0625 + 24 88 (E = 40) Δ = 48 BCS231024-Ausland STR 195 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 1 40 0.25 20 0.0625 0 Clethodim 24 0 8 0 A1 & Clethodim 1 + 24 40 (E = 20) Δ = 20 1 + 8 60 (E = 20) Δ = 40 0.25 + 24 10 (E = 0) Δ = 10 0.25 + 8 10 (E = 0) Δ = 10 0.0625 + 24 60 (E = 40) Δ = 20 0.0625 + 8 60 (E = 40) Δ = 20 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 0.25 40 Dicamba 15 50 5 40 A1 & Dicamba 0.25 + 15 88 (E = 70) Δ = 18 0.25 + 5 75 (E = 64) Δ = 11 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 21 DAT A1 1 40 Dicamba 15 50 5 40 A1 & Dicamba 1 + 15 75 (E = 70) Δ = 5 1 + 5 80 (E = 64) Δ = 16 Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 10 DAT A1 0.25 80 0.0625 50 Diflufenican 120 25 A1 & Diflufenican 0.25 + 120 95 (E = 85) Δ = 10 0.0625 + 120 70 (E = 62.5) Δ = 7.5 Active ingredient Application rate Herbicidal activity [%] against g ai / ha PHBPU 21 DAT A1 0.0625 0 Diflufenican 360 40 120 20 A1 & Diflufenican 0.0625 + 360 70 (E = 40) Δ = 30 0.0625 + 120 30 (E = 20) Δ = 10 BCS231024-Ausland STR 196 Active ingredient Application rate Herbicidal effect [%] against g ai / ha PHBPU 10 DAT A1 1 85 0.25 30 Dimethenamid 120...

Claims

BCS231024-Ausland STR 217 Claims 1. Composition containing herbicidally active compounds (A) and (B) where (A) represents one or more compounds of the general formula (I) or their agrochemically acceptable salts, where R 1für Wasserstoff, Fluor, Chlor, Brom, Iod, Cyan Moe,thyl, Ethyl, Prop-1-yl, 1- Methylethyl, But-1-yl, 1-Methylpropyl, 2-Methylproypl, 1,1-Dimethylethyl, n-Pentyl, 1- Methylbutyl, 2-Methylbutyl, 3-Methylbutyl, 1,1-Dimtheylpropyl, 1,2-Dimethylpropyl, 2,2-Dimethylpropyl, 1-Ethylpropyl, n-Hexyl, 1-Methlpyentyl, 2-Methylpentyl, 3- Methylpentyl, 4-Methylpentyl, 1,1-Dimethylbutyl,21-,Dimethylbutyl, 1,3-Di- methylbutyl, 2,2-Dimethylbutyl, 2,3-Dimethylbuty 3l,,3-Dimethylbutyl, 1-Ethylbutyl, 2- Ethylbutyl, 1,1,2-Trimethylpropyl, 1,2,2-Trimethyrloppyl, 1-Ethyl-1-methylpropyl, 1- Ethyl-2-methylpropyl, Trifluormethyl, Difluormethy,l Pentafluorethyl, 2,2-Difluorethyl, 2,2,2-Trifluorethyl, Methoxy, Ethoxy, Prop-1-ylox Py,rop-2-yloxy, But-1-yloxy, But-2- yloxy, 2-Methylprop-1-yloxy, 1,1-Dimethyleth-1-yloyx, Difluormethoxy, Trifluormethoxy, Pentafluorethoxy, 2,2-Difluorethyo,x 2,2,2-Trifluorethoxy steht, R 2represents hydrogen, fluorine, chlorine, bromine, methyl, trimethyl, methoxy, ethoxy, prop-1-yloxy, but-1-yloxy, R 3 represents hydrogen, fluorine, chlorine, bromine, methoxy, ethoxy, prop-1-yloxy, prop-2-yloxy, but-1-yloxy, but-2-yloxy, 2-methylprop-1-yloxy, 1-,1-dimethyleth-1-yloxy, R 4 represents fluorine, chlorine, bromine, cyano, N2O, C(O)NH2, C(S)NH2, trifluoromethyl, difluoromethyl, pentafluoroethyl, ethynyl, propyn-1l, -y 1-butyn-1-yl, pentyn-1-yl, hexyn-1-yl, BCS231024-Abroad STR 218 R 5 , R 6 and R 7unabhängig voneinander für Wasserstoff, Fluor,o Cr,h Blrom, Iod, Cyano, Methyl, Ethyl, Prop-1-yl, 1-Methylethyl, But-1-y 1l,-Methylpropyl, 2-Methylpropyl, 1,1-Dimethylethyl, n-Pentyl, 1-Methylbutyl, 2-Metlhbyutyl, 3-Methylbutyl, 1,1- Dimethylpropyl, 1,2-Dimethylpropyl, 2,2-Dimethylpproyl, 1-Ethylpropyl, n-Hexyl, 1- Methylpentyl, 2-Methylpentyl, 3-Methylpentyl, 4-Mheytlpentyl, 1,1-Dimethylbutyl, 1,2-Dimethylbutyl, 1,3-Di-methylbutyl, 2,2-Dimethbyultyl, 2,3-Dimethylbutyl, 3,3- Dimethylbutyl, 1-Ethylbutyl, 2-Ethylbutyl, 1,1,2-Timrethylpropyl, 1,2,2- Trimethylpropyl, 1-Ethyl-1-methylpropyl, 1-Ethyl-m2-ethylpropyl, Trifluormethyl, Difluormethyl, Pentafluorethyl, 2,2-Difluorethyl,22,2-Trifluorethyl, Methoxy, Ethoxy, Prop-1-yloxy, Prop-2-yloxy, But-1-yloxy, But-2-yloyx, 2-Methylprop-1-yloxy, 1,1- Dimethyleth-1-yloxy, Difluormethoxy, Trifluormethoyx, Pentafluorethoxy, 2,2-Difluorethoxy, 2,2,2-Trifluorethoxy stehen, G für Methylen, (Methyl)methylen, (Ethyl)methyle (nP,rop-1-yl)methylen,(Prop-2- yl)methylen, (But-1-yl)methylen, (But-2-yl)methyl,e (nPent-1-yl)methylen, (Pent-2- yl)methylen, (Pent-3-yl)methylen, (Dimethyl)methny,le (Diethyl)methylen, Ethylen, n- Propylen, (1-Methyl)ethyl-1-en, (2-Methyl)ethyl-1n-,e n-Butylen, 1-Methylpropyl-1-en, 2-Methylpropyl-1-en, 3-Methylpropyl-1-en, 1,1-Dimheytlethyl-1-en, 2,2-Dimethylethyl- 1-en, 1-Ethylethyl-1-en, 2-Ethylethyl-1-en, 1-(P-r1o-pyl)ethyl-1-en, 2-(Prop-1-yl)ethyl- 1-en, 1-(Prop-2-yl)ethyl-1-en, 2-(Prop-2-yl)ethy-le-1n, 1,1,2-Trimethylethyl-1-en, 1,2,2- Trimethylethyl-1-en, 1,1,2,2-Tetramethylethyl-1-e nn-P,entylen, 1-Methylbutyl-1-en, 2- Methylbutyl-1-en, 3-Methylbutyl-1-en, 4-Methylbu-ty1l-en, 1,1-Dimethylpropyl-1-en, 2,2-Dimethylpropyl-1-en, 3,3-Dimethylpropyl-1-en,,21-Dimethylpropyl-1-en, 1,3- Dimethylpropyl-1-en, 1-Ethylpropyl-1-en, n-Hexyle 1n-,Methylpentyl-1-en, 2- Methylpentyl-1-en, 3-Methylpentyl-1-en, 4-Methylptyeln-1-en, 1,1-Dimethylbutyl-1-en, 1,2-Dimethylbutyl-1-en, 1,3-Di-methylbutyl-1-en,22-D,1-methylbutylene, 2,3-dimethylbutylene, 3,3-dimethylbutylene, 1-ethylbutylene, 2-ethylbutylene, 1,1,2-trimethylpropylene, 1,2,2-trimethylpropylene, 1-ethyl-1-methylpropylene, 1-ethyl-2-methylpropylene, X and Y independently represent O (oxygen fluoride) or S (sulfur) and, BCS231024-Ausland STR 219 Q stands for one of the following specifically named guidlines Q-1 to Q-25, where i n den Strukturformeln der nachfolgenden Tabellre P dfe il für eine Bindung der respective group Q to the carbonyl group in the general formula (I): Q-1 Q-2 Q-3 Q-4 Q-5 Q-6 Q-7 Q-8 Q-9 Q-10 Q-11 Q-12 Q-13 Q-14 Q-15 Q-16 Q-17 Q-18 Q-19 Q-20 Q-21 Q-22 Q-23 Q-24 Q-25 and (B) represents one or more herbicides from the group of derbicidal active ingredients (B1) to (B11), wherein BCS231024-Ausland STR 220 (B1) for herbizide Wirkstoffe aus der Gruppe decrh nfaolgend genannten 1,3-Diketoverbindungen steht (B1.1) Alloxydim, (CAS 55634-91-8), (CAS 55635) (B136.275) Bicyclopyrone, (CAS 352010-68-5) (B1.3) Butroxydim, (CAS 138164-12-2) (B1.4) Clethodim, (CAS 99129-21-2) (B1.5) Cycloxydim, (CAS 101-2015) (B1.3) Fenquinotrione, (CAS 1342891-70-6) (B1.7) Mesotrione, (CAS 104206-82-8) (B1.8) Pinoxaden, (CAS 243973-20-8) (B1.9) Profoxydim, (CAS 139.01-31) (B1.1) Sethoxydim, (CAS 74051-80-2) (B1.11) Sulcotrione, (CAS 99105-77-8) (B1.12) SYP-9121 (CAS 1976053-87-8) (B1.13) Tefuryltrione, (CAS 74051-80-17) (B1.16) Tembotrione, (CAS 335104-84-2) (B1.15) Tepraloxidim, (CAS 149979-41-9) (B1.16) Tralkoxydim, (CAS 87820-88-0) (B1.17) Y13161, (CAS 13948) (B1.146)-61-41-9 Y13287 (CAS 1639426-42-8) (B2) for herbizide active ingredients from the group decrh nfaolgend genannten (Sulfon)Amide steht (B2.1) Acetochlor, (CAS 34256-82-1) (B2.1) Alachlor, (2CAS) 15972-60-8) (B2.3) Amidosulfuron, (CAS 120923-37-7) (B2.4) Asulam, (CAS 3337-71-1), (CAS 14089-43-1), (CAS 2302-17-2) (B2.5) Azimsulfuron, (CAS 120162-55-2) (B2.6) Beflubutamid, (CAS 113614-08-7), (CAS 113614-09-8) (B2.7) Bensulfuron, (CAS 83055-99-6), (CAS 83055-99-6) (B2.8) Butachlor, (CAS 23184-66-99). BCS231024-Ausland STR 221 (B2.9) Carbetamide, (CAS 16118-49-3) (B2.10) Chlorimuron, (CAS 99283-00-8), (CAS 90982-32-4) (B2.11) Chlorpropham, (CAS 101-21-3) (B2.12) Chlorsulfuron, (CAS 64902-72-3) (B2.13) Cinosulfuron, (CAS 94593-91-6) (B2.14) Cloransulam, (CAS159518-97-5), (CAS 147150-35-4) (B2.15) Cyclosulfamuron, (CAS 136849-15-5) (B2.16) Desmedipham, (CAS 13684-56-5) (B2.17) Diclosulam, (CAS 145701-21-9) (B2.18) Diflufenican, (CAS 83164-33-4) (B2.19) Dimethachlor, (CAS 50563-36-5) (B2.20) Dimethenamid, (CAS 87674-68-8), (CAS 163515-14-8) (B2.21) Esprocarb (CAS 85785-20-2) (B2.22) Ethametsulfuron, (CAS 111353-84-5), (CAS 97780-06-8) (B2.23) Ethoxysulfuron, (CAS 126801-58-9) (B2.24) Flazasulfuron, (CAS 104040-78-0) (B2.25) Florasulam, (CAS 145701-23-1) (B2.26) Flucarbazone, (CAS 145026-88-6), (CAS 181274-17-9) (B2.27) Flucetosulfuron, (CAS 412928-75-7) (B2.28) Flufenacet, (CAS 142459-58-3) (B2.29) Flumetsulam, (CAS 98967-40-9) (B2.30) Flupyrsulfuron, (CAS 150315-10-9), (CAS 144740-53-4), (CAS 144740-54-5) (B2.31) Foramsulfuron, (CAS 173159-57-4) (B2.32) Halosulfuron, (CAS 135397-30-7), (CAS 100784-20-1) (B2.33) Imazosulfuron, (CAS 122548-33-8) (B2.34) Iodosulfuron, (CAS 185119-76-0), (CAS 144550-06-1), (CAS 144550-36-7). BCS231024-Ausland STR 222 (B2.35) Ipfencarbazone, (CAS 212201-70-2) (B2.36) Mefenacet, (CAS 73250-68-7) (B2.37) Mesosulfuron, (CAS 400852-66-6), (CAS 208465-21-8) (B2.38) Metazachlor, (CAS 67129-08-2) (B2.39) Metazosulfuron, (CAS 868680-84-6) (B2.40) Metolachlor, (CAS 51218-45-2) (B2.41) Metosulam, (CAS 139528-85-1) (B2.42) Metsulfuron, (CAS 79510-48-8), (CAS 74223-64-6) (B2.43) Nicosulfuron, (CAS 111991-09-4) (B2.44) Orthosulfamuron, (CAS 213464-77-8) (B2.45) Oxasulfuron, (CAS 144651-06-9) (B2.46) Penoxsulam, (CAS 219714-96-2) (B2.47) Pethoxamide, (CAS 106700-29-2) (B2.48) Phenmedipham, (CAS 13684-63-4) (B2.49) Picolinafen, (CAS 137641-05-5) (B2.50) Pretilachlor, (CAS 51218-49-6) (B2.51) Primisulfuron, (CAS 113036-87-6), (CAS 86209-51-0) (B2.52) Propachlor, (CAS 1918-16-7) (B2.53) Propanil, (CAS 709-98-8) (B2.54) Propham, (CAS 122-42-9) (B2.55) Propisochlor, (CAS 86763-47-5) (B2.56) Propoxycarbazone, (CAS 145026-81-9), (CAS 181274-15-7) (B2.57) Propyrisulfuron, (CAS 570415-88-2) (B2.58) Propyzamide, (CAS 23950-58-5) (B2.59) Prosulfocarb, (CAS 52888-80-9) (B2.60) Prosulfuron, (CAS 94125-34-5) (B2.61) Pyrazosulfuron, (CAS 98389-04-9), (CAS 93697-74-6) (B2.62) Pyroxsulam, (CAS 422556-08-9) (B2.63) Rimsulfuron, (CAS 122931-48-0) (B2.64) S-metolachlor, (CAS 87392-12-9). BCS231024-Ausland STR 223 (B2.65) Sulfometuron, (CAS 74223-56-6), (CAS 74222-97-2), (CAS 144651-06-9) (B2.66) Sulfosulfuron, (CAS 141776-32-1) (B2.67) Thenylchlor, (CAS 96491-05-3) (B2.68) Thiencarbazone, (CAS 936331-72-5), (CAS 317815-83-1) (B2.69) Thifensulfuron, (CAS 79277-67-1), (CAS 79277-27-3) (B2.70) Tri-allat, (CAS 2303-17-5) (B2.71) Triasulfuron, (CAS 82097-50-5) (B2.72) Tribenuron, (CAS 106040-48-6), (CAS 101200-48-0) (B2.73) Trifloxysulfuron, (CAS 145099-21-4, (CAS 199119-58-9) (B2.74) Triflusulfuron, (CAS 135990-29-3), (CAS 126535-15-7) (B2.75) Tritosulfuron, (CAS 142469-14-5) (B2.76) Esprocarb, (CAS 85785-20-2) (B2.77) Profluazol, (CAS 190314-43-3) (B2.78) Tri-allate, (CAS 2303-17-5) (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5- methoxy-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5- vinyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.81) Icafolin-methyl (CAS 2749998-21-6, (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l- methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)- vinyl-4H-isoxazol-5-carbonyl]amino]-2,3- dihydrofuran-5-carboxylat,. BCS231024-Ausland STR 224 (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)- methyl-4H-isoxazol-5-carbonyl]amino]-2,3- dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5- vinyl-4H-1,2-oxazol-5-yl]carbonyl]amino]- cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-5- methoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o- fluorphenyl)-5-(trifluormethyl)-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl- 4H-1,2-oxazol-5-yl]carbonyl]amino]cyclopenten-1- carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-l5)- methyl-4H-1,2-oxazol-5-yl]carbonyl]amino]- cyclopenten-1-carboxylat, (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2- ylcarbonyl)cyclopent-2-en-1-yl]-5-(trifluormethyl)- 4H-1,2-oxazol-5-carboxamid, (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4- [(propylsulfonylamino)carbonyl]cyclopent-2-en-1- yl]-5-(trifluormethyl)-4H-1,2-oxazol-5-carboxamid, (B2.92) (1S,4R)-4-[[(5R)-3-(3,5-difluorophenyl)-5e-mthyl- 4H-isoxazol-5-carbonyl]amino]cyclopent-2-ene-1- carbonsäure (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl)-[-(3S)- methylsulfinyl]-4-(trifluormethyl)benzamid, (B3) für herbizide Wirkstoffe aus der Gruppe decrh nfaolgend genannten Arylnitrile steht (B3.1) Bromoxynil, (CAS 1689-84-5) (CAS 3861-41-4), (CAS 56634-95-8), (CAS 1689-99-2), (CAS 2961-68-4) (B3.2) Chlorthiamid, (CAS 1918-13-4) (B3.3) Dichlobenil, (CAS 1194-65-6). BCS231024-Ausland STR 225 (B3.4) Ioxynil, (CAS 1689-83-4), (CAS 2961-61-7), (CAS 3861-47-0), (CAS 2961-62-8) (B3.5) Pyraclonil (CAS 158353-15-2) (B4) for herbizide Wirkstoffe aus der Gruppe decrh nfaolgend genannten Azole steht (B4.1) Amicarbazone, (CAS 129909-90-6) (B4.2) Amitrole, (CAS 61-82-5) (B4.3) Azafenidin, (CAS 68049-83-2) (B4.4) Benzofenap, (CAS 82692-44-2) (B4.5) Benzuofucaotong (CAS 1992017-55-6) (B4.6) Biscarfentrazone (CAS 1622908-18-2) (B4.7) Cafenstrole, (CAS 125306-83-4) (B4.8) Carfentrazone, (CAS 128621-72-7), (CAS128-0623-91) (B4.9) Fentrazamide, (CAS 158237-07-1) (B4.10) Imazamethabenz, (CAS 100728-84-5), (CAS0851-845-8) (B4.11) Imazamox, (CAS 114311-32-9), (CAS 247057-3-2)2 (B4.12) Imazapic, (CAS 104098-48-8), (CAS 115136-3-5)3 (B4.13) Imazapyr, (CAS 81334-34-1), (CAS 81510-8)3-0 (B4.14) Imazaquin, (CAS 81335-37-7), (CAS 813359-4),7- (CAS 81335-43-5), (CAS 81335-46-8) (B4.15) Imazethapyr, (CAS 81335-77-5), (CAS 10196167-2-) (B4.16) Isouron, (CAS 55861-78-4) (B4.17) Isoxaben, (CAS 82558-50-7) (B4.18) Isoxaflutole, (CAS 141112-29-0) (B4.19) Oxadiargyl, (CAS 39807-15-3) (B4.20) Oxadiazon, (CAS 19666-30-9) (B4.21) Pyraflufen, (CAS 129630-17-7), (CAS 12961390--9) (B4.22) Pyrasulfotole, (CAS 365400-11-9) (B4.23) Pyrazolynate, (CAS 58011-68-0) (B4.24) Pyrazoxyfen, (CAS 71561-11-0) (B4.25) Pyroxasulfone, (CAS 447399-55-5) (B4.26) Sulfentrazone, (CAS 122836-35-5) (B4.27) Tolpyralate, (CAS 1101132-67-5) (B4.28) Topramezone, (CAS 210631-68-8) (B4.29) Triazolesulcotrione (CAS 1911613-97-2) (QYR-301),. BCS231024-Ausland STR 226 (B4.30) QYM-201, (CAS 1855925-45-1) (B4.31) Bencarbazone, (CAS 173980-17-1) (B4.32) Fluazolate, (CAS 174514-07-9) (B4.33) Flupoxam, (CAS 119126-15-7) (B4.34) Isoxachlortole (CAS 141112-06-3) (B5) stands for further herbicides listed below, (B5.1) Aminocyclopyrachlor, (CAS 858956-08-8), (CAS 858954-83-3), (CAS 858956-35-1) (B5.2) Aminopyralid, (CAS 150114-71-9), (CAS 5661-8971-5), (CAS 566191-89-7) (B5.3) Benazolin-ethyl, (CAS 3813-05-6), (CAS 385-7661-1), (CAS 25059-80-7), (CAS 67338-65-2) (B5.4) Benfluralin, (CAS 1861-40-1) (B5.5) Bentazone, (CAS 25057-89-0), (CAS 50723-)80-3 (B5.6) Benzobicyclon, (CAS 156963-66-5) (B5.7) Bixlozone (CAS 81777-95-9) (B5.8) Bromofenoxime, (CAS 13181-17-4) (B5.9) Butralin, (CAS 33629-47-9) (B5.10) Chloridazon / Pyrazone, (CAS 1698-60-8) (B5.11) Chlorthal, (CAS 2136-79-0), (CAS 1861-32,-1) (CAS 887-54-7) (B5.12) Cinidon-ethyl, (CAS 142891-20-1) (B5.13) Cinmethylin, (CAS 87818-31-3) (B5.14) Clomazone, (CAS 81777-89-1) (B5.15) Cyclopyrimorat, (CAS 499231-24-2) (B5.16) Dinitramine, (CAS 29091-05-2) (B5.17) Diquat, (CAS 277-27), (CAS-27-26) 85-00-7), (CAS 4032-26-2) (B5.18) Dithiopyr, (CAS 97886-45-8) (B5.19) Acetic acid, (CAS 64-19-7) (B5.20) Ethalfluralin, (CAS 5528-26) (B5.26) Ethofumesate, (CAS 26225-79-6) (B5.22) Flamprop, (CAS 58667-63-3, (CAS 90134-5,9-1) (CAS 63782-90-1), (CAS 63729-98-6) (B5.CAS.23) Flora (CAS. 943832-81-3), (CAS 1036961-72-9). BCS231024-Ausland STR 227 (B5.24) Flufenpyr, (CAS 188490-07-5), (CAS 1884879--80) (B5.25) Flumiclorac, (CAS 87547-04-4), (CAS 87548-716) (B5.26) Flumioxazine, (CAS 103361-09-7) (B5.27) Fluridone, (CAS 59756-60-4) (B5.28) Flurochloridone, (CAS 61213-25-0) (B5.29) Flurtamone, (CAS 965-45) (B5.25) (B5.28) Fluthiacet-methyl, (CAS 149253-65-6) (B5.31) Halauxifen, (CAS 943832-60-8), (CAS 94389381--9) (B5.32) Indanofan, (CAS 13320-30-1) (CASBflurazone, 33) 27314-13-2) (B5.34) Oleic acid (CAS 112-80-1) (B5.35) Oryzalin, (CAS 19044-88-3) (B5.36) Oxaziclomefone, (CAS 153197-14-9) (B5.37) Paraquat (CAS 112-80-1) 4685-14-7), (CAS 1910-42-5), (CAS 2074-50-2) (B5.38) Pelargonsäure, (CAS 112-05-0) (B5.39) Pendimethalin, (CAS 40487-42-1) (B5.40) (CAS, Pentoxazone. 110956-75-7) (B5.41) Pyridafol, (CAS 40020-01-7) (B5.42) Pyridate, (CAS 55512-33-9) (B5.43) Tetflupyrolimet, (CAS 2053901-33-8) (BAS) (CAS 4053944, Thiazol. 117718-60-2) (B5.45) Triaphamone, (CAS 874195-61-6) (B5.46) Trifluralin, (CAS 1582-09-8) (B5.47) 4-Amino-3-chloro-5-fluoro- 6-(7-fluoro-1H-indol-6- yl)pyridine-2-carbonsäure (B5.48) Cyclopyrimorate, (CAS 499231-24-2) (B5.49) Diquat, (CAS 2764-72-9), (CAS 85-00-7), (CAS4032-26-2) (B5.50) Oxaziclomefone, (CAS 153197-14-9) (B5.51) Pentanochlor, (CAS 2307-68-8) (B5.52) Tebutam, (CAS 35256-85-0) (B5.53) Thidiazimin, (CAS 123249-43-4). BCS231024-Ausland STR 228 (B5.54) 4-Hydroxy-1-methyl-3-[4- (CAS 1708087-22-2) (trifluoromethyl)-2- pyridinyl]-2-imidazolidinon ( B5.55) MSMA (CAS 2163-80-6)(B6) herbicidal active ingredients from the group of the (het)arylcarboxylic acids mentioned below are (B6.1) Chloramben, (CAS 133-90-4), (CAS 1076-46-6), (CAS 53404-16-3), (CAS 7286-84-2), (CAS 25182-03-0), (1954-81-0) (B6.2) Clopyralid, (CAS 1702-17-6 ()C, AS 1532-24-7), (CAS 57754-85-5), (CAS 58509-83-4), (CAS 73455-09-1) (B6.3) Dicamba, (CAS 1918-00-9 ()C, AS 1286239-22-2), (CAS 104040-79-1), (CAS 2300-66-5), (CAS 25059-78-3), (CAS 55871-02-8), (CAS 6597-78-0), (CAS 53404-28-7), (CAS 10007-85-9), (CAS 1982-69-0), (53404-29-8), (CAS 56141-00-5) (B6.4) Fluroxypyr, (CAS 69377-81-7), (CAS -27-8), (CAS 81406-37-3) (B6.5) Picloram, (CAS 1918-02-1), (CAS 55870-98-9), (CAS 36374-99-9), (CAS 26952-20-5), (CAS 14143-55-6), (CAS 55871-00-6), (CAS 2545-60-0), (CAS 35832-11-2), (CAS 6753-47-5), (CAS 82683-78-1) (B6.6) Quinclorac, (CAS 84087-01-4), (CAS 84087-94)8,- (CAS 84087-33-2) (B6.7) Quinmerac, (CAS 90717-03-6) (B6.8) TBA, (CAS 50-31-7), (CAS 3426-62-8), (CAS 71750-37-3), (CAS 4559-30-2), (CAS 2078-42-4) (B6.9) Triclopyr (CAS 55335-06-3), (CAS [64700-56],-7 (CAS 1048373-85-8), (CAS 60825-27-6), (CAS 57213-69-1). BCS231024-Ausland STR 229 (B7) for herbicidal active ingredients from the group of the following organic phosphorus compounds stands (B7.1) Anilofos, (CAS 64249-01-0) (B7.2) Bialaphos, (CAS 35597-43-4), (CAS 71048-9)9-2 (B7.3) Butamifos, (CAS 36335-67-8) (B7.4) Glufosinate, (CAS 51276-47-2), (CAS 35597-5-4)4, (CAS 77182-82-2) (CAS 70033-13-5) (B7.5) Glyphosate, (CAS 1071-83-6), (CAS 69254-4),0-6 (CAS 34494-04-7), (CAS 38641-94-0), (CAS 40465-66-5), (CAS 39600-42-5), (CAS 70393-85-0), (CAS 81591-81-3) (B7.6) Piperophos, (CAS 24151-93-7) (B7.7) Sulfosate, (CAS 1591-81-3) (B7.8) Amiprofos (CAS 33857-23-7, (CAS 36001-88-4) (B8) stands for herbicidal active ingredients from the group of the phenyl ethers mentioned below (B8.1) 2,4-D, (CAS 94-75-7), (CAS 2307-55-3), (CAS 1929-73-3), (CAS 1320-18-9), (CAS 1928-45-6), (CAS 94-80-4), (CAS 1048373-72-3), (CAS 20940-37-8), (CAS 2008-39-1), (CAS 5742-19-8), (CAS 2212-54-6), (CAS 533-23-3), (CAS 1928-43-4), (CAS 37102-63-9), (CAS 713-15-1), (CAS 25168-26-7), (CAS 94-11-1), (CAS 5742-17-6), (CAS 3766-27-6), (CAS 1917-97-1), (CAS 1928-38-7), (CAS 1928-44-5), (CAS 1917-92-6), (CAS 1928-61-6), (CAS 2702-72-9), (CAS 15146-99-3), (CAS 28685-18-9), (CAS 2646-78-8), (CAS 18584-79-7), (CAS 2569-01-9), (CAS 215655-76-8) (B8.2) 2,4-DB, (CAS 94-82-6), (CAS 2758-42-1), (CAS 1320-15-6), (CAS 19480-40-1), (CAS 10433-59-7). BCS231024-Ausland STR 230 (B8.3) 2,4-DP, (CAS 120-36-5), (CAS 53404-31-2), (CAS 53404-32-3), (CAS 79270-78-3), (CAS 28631-35-8), (CAS 57153-17-0), (CAS 5746-17-8), (CAS 39104-30-8) (B8.4) Acifluorfen, (CAS 50594-66-6), (CAS 50594-67)7, (CAS 62476-59-9) (B8.5) Aclonifen, (CAS 74070-46-5) (B8.6) Bifenox, (CAS 42576-02-3) (B8.7) Chlomethoxyfen, (CAS 32861-85-1) (B8.8) Clodinafop- (CAS 114420-56-3), (CAS 105512-06-9) propargyl, (B8.9) Clomeprop, (CAS 84496-56-0) (B8.10) Cyhalofop, (CAS 122008-78-0), (CAS 1220058-9-8) (B8.11) Diclofop, (CAS 40843-25-2), (CAS 51338-2)7-3 (B8.12) Ethoxyfen, (CAS 188634-90-4), (CAS 1310826-5-4) (B8.13) Fenoxaprop, (CAS 95617-09-7), (CAS 113150-80-)4, (CAS 71283-80-2) (B8.14) Fluazifop, (CAS 69335-91-7), (CAS 83066-08)8,- (CAS 79241-46-6) (B8.15) Fluoroglycofen, (CAS 77501-60-1), (CAS 771-5900-7) (B8.16) Fomesafen, (CAS 72178-02-0), (CAS 10873-10-)70 (B8.17) Halosafen, (CAS 77227-69-1) (B8.18) Haloxyfop, (CAS 69806-34-4), (CAS 95977-02)9,- (CAS 72619-32-0) (B8.19) Lactofen, (CAS 77501-63-4) (B8.20) MCPA, (CAS 94-74-6), (CAS 19480-43-4), (CAS 1713-12-8), (CAS 2039-46-5), (CAS 20405-19-0), (CAS 2698-38-6), (CAS 29450-45-1), (CAS 1713-11-7), (CAS 26544-20-7), (CAS 2698-40-0), (CAS 2436-73-9), (CAS 6365-62-4), (CAS 5221-16-9), (CAS 3653-48-3), (CAS 42459-68-7) (B8.21) MCPB, (CAS 94-81-5), (CAS 10443-70-6), (CAS 57153-18-1), (CAS 6062-26-6) (B8.22) Mecoprop, (CAS 93-65-2), (CAS 32351-70-5),. BCS231024-Foreign STR 231 (CAS 1432-14-0), (CAS 71526-69-7), (CAS 28473-03-2), (CAS 2786-19-8), (CAS 1929-86-8), (CAS 19095-88-6), (CAS 53404-61-8), (CAS 16484-77-8) (B8.23) Metamifop, (CAS 256412-89-2) (B8.24) Oxyfluorfen, (CAS 42874-03-3) (B8.25) Propaquizafop, (CAS 111479-05-1) (B8.26) Quizalofop, (CAS 76578-12-6), (CAS 765748--81), (B8.27) Quizalofop-P, (CAS 94051-08-8), (CAS 100-65416-3), (CAS 200509-41-7) (B8.28) Benzfendizone (CAS 158755-95-4) (B9) represents herbicidal active ingredients from the group of the pyrimidines / triazines mentioned below: (B9.1) Bispyracsodium, (CAS 125401-92-5) (B9.2) Bromacil, (CAS 314-40-9), (CAS 53404-19-6), (CAS 69484-12-4) (B9.3) Butafenacil, (CAS 134605-64-4) (B9.4) Lenacil, (CAS 2164-08-1) (B9.5) Pyribenzoxime, (CAS 168088-61-7) (B9.6) Pyriftalid, (CAS 135186-78-6) (B9.7) Pyriminobac, (CAS 136191-56-5), (CAS 136191- 64-5) (B9.8) Pyrimisulfan, (CAS 221205-90-9) (B9.9) Pyrithiobac-sodium, (CAS 123342-93-8), (C 1A2S3343- 16-8) (B9.10) Saflufenacil, (CAS 372137-35-4) (B9.11) Terbacil, (CAS 5902-51-2) (B9.12) Tiafenacil, (CAS 1220411-29-9) (B9.13) Trifludimoxazin, (CAS 1258836-72-4) (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1- (CAS 353292-31-6) methyl-6-trifluoromethyl-2,4-dioxo- 1,2,3,4-tetrahydropyrimidin-3- yl)phenoxy]-2-pyridyloxy]acetat (B9.15) Ethyl-3-{2-chlor-4-fluor-5-[3- (CAS 1949837-17-5) methyl-2,6-dioxo-4-(trifluormethyl)- 3,6-dihydropyrimidin-1(2H)-. BCS231024-Ausland STR 232 yl]phenyl}-5-methyl-4,5-dihydro- 1,2-oxazole-5-carboxylate (B9.16) 3-[2-chloro-5-(3,5-dimethyl-2,6- (CAS 2558200-03-4) dioxo-4-sulfanylidene-1,3,5- triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4- (CAS 2669111-31-1) fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidine-1(2H)- yl]benzylidene}amino]oxy}propanoate (B9.18) Flufenoximacil (CAS 2759011-88-4) (B10) stands for herbicidal active ingredients from the group of the following (thio)ureas: (B10.1) Chlorobromuron, (CAS 13360-45-7) (B10.2) Chlorotoluron, (CAS 15545-48-9) (B10.3) Daimuron, (CAS 42609-52-9) (B10.4) Dimefuron, (CAS 34205-21-5) (B10.5) Diuron, (CAS 330-54-1) (B10.6) Diflufenzopyr (CAS 1957168-02-3) (B10.7) Fluometuron, (CAS 2164-17-2) (B10.8) Isoproturon, (CAS 34123-59-6) (B10.9) Linuron, (CAS 330-55-2) (B10.10) Methabenzthiazuron, (CAS 18691-97-9) (B10.11) Metobromuron, (CAS 3060-89-7) (B10.12) Metoxuron, (CAS 19937-59-8) (B10.13) Monolinuron, (CAS 1746-81-2) (B10.14) Neburon, (CAS 555-37-3) (B10.15) Siduron, (CAS 1982-49-6) (B10.16) Tebuthiuron, (CAS 34014-18-1) (B10.17) Fenuron, (CAS 101-42-8) (B10.18) Chloroxuron, (CAS 1982-47-4) (B10.19) Diflufenzopyr, (CAS 1957168-02-3, CAS 109293-98-3) (B10.20) Ethidimuron (CAS 30043-49-3). BCS231024-Ausland STR 233 (B11) for herbicidal active ingredients from the group of the following triazines stands (B11.1) Ametryne, (CAS 834-12-8) (B11.2) Atrazine, (CAS 1912-24-9) (B11.3) Cyanazine, (CAS 21725-46-2) (B11.4) Dimethametryn, (CAS 22936-75-0) (B11.5) Hexazinone, (CAS 51235-04-2) (B11.6) Indaziflam, (CAS 950782-86-2) (B11.7) Metamitron, (CAS 41394-05-2) (B11.8) Metribuzin, (CAS 21087-64-9) (B11.9) Prometon, (CAS 1610-18-0) (B11.10) Prometryne, (CAS 7287-19-6) (B11.11) Propazine, (CAS 139-40-2) (B11.12) Simazine, (CAS 122-34-9) (B11.13) Simetryne, (CAS 1014-70-6) (B11.14) Terbumetone, (CAS 33693-04-8) (B11.15) Terbuthylazine, (CAS 5915-41-3) (B11.16) Terbutryne, (CAS 886-50-0) (B11.17) Triaziflam, (CAS 131475-57-5) (B11.18) Trietazine, (CAS 1912-26-1) (B11.19) Desmetryne (CAS 1014-69-3).

2. Composition according to claim 1, wherein the compound (A) of the general formula (I) is defined in that R 1 stands for hydrogen, R 2 stands for fluorine, R3 stands for fluorine, R 4 for chlorine, bromine, cyano, N 2 O stands, R 5 stands for hydrogen, R 6 for hydrogen, fluorine, chlorine, bromine or cyano BCS231024-Abroad STR 234 R 7 represents hydrogen, G represents methylene or (methyl)methylene, X represents O (oxygen) or S (sulfur), Y represents O (oxygen), and Q represents one of the groups Qg-1 to Q-25 mentioned in claim 1.

3. Composition according to claim 1, wherein the compound (A) of the general formula (I) is defined in that R 1 stands for hydrogen, R 2 stands for fluorine, R 3 stands for fluorine, R 4 stands for chlorine, bromine, cyano, R 5 stands for hydrogen, R 6 represents hydrogen, fluorine, R 7 stands for hydrogen, G stands for methylene, X stands for O (oxygen), Y stands for O (oxygen) and BCS231024-Ausland STR 235 Q represents one of the groups Qg-1, Q-2, Q-4, Q-5, Q-6, Q-7, Q-8, Q-9, Q-10, Q-12, Q-13, Q-14, Q-15, Q-16, Q-18 or Qd-e1r9 mentioned in claim 1.

4. Composition according to claim 1, wherein the compound (A) corresponds to the general formula (I) cyclopropylmethyl (2-{2-chloro-4-fluoro-5-[3-methyl-,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenoxy}phenoxy) acetate.

5. Composition according to one of the preceding claims 1 to 4, wherein the compound (B) contains one or more active ingredients selected from the group (B1.2) Bicyclopyrone, (B1.4) Clethodim, (B1.7) Mesotrione, (B1.8) Pinoxaden, (B1.14) Tembotrione, (B2.1) Acetochlor, (B2.18) Diflufenican, (B2.20) Dimethenamid, (B2.24) Flazasulfuron, (B2.28) Flufenacet, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.40) Metolachlor, (B2.43) Nicosulfuron, (B2.48) Phenmedipham, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.79) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-methoxy-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat,. BCS231024-Ausland STR 236 (B2.80) Methyl rel-(2R,4R)-4-[[3-(3,5-dichloropheln)-y5-vinyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.81) Icafolin-methyl, (B2.82) Isopropyl rel-(2R,4R)-4-[[3-(3-fluorophen)-y5l-methyl-4H-isoxazol-5- carbonyl]amino]tetrahydrofuran-2-carboxylat, (B2.83) Methyl (3R)-3-[[(5S)-3-(3,5-difluoropheny-5l)-vinyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.84) Methyl (3R)-3-[[(5R)-3-(3,5-difluoropheny-5l)-methyl-4H-isoxazol-5- carbonyl]amino]-2,3-dihydrofuran-5-carboxylat, (B2.85) Methyl (1S,4R)-4-[[[(5S)-3-(3,5-difluorphyeln)-5-vinyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopent-2-en-1-carboxylat, (B2.86) Ethyl (1S,4R)-4-[[[3-(3,5-difluorphenyl)-m5-ethoxy-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopent-2-en-1-carboxylat, (B2.87) 2-Methoxyethyl (1S,4R)-4-[[[(5R)-3-(3-cya-n5o-fluorphenyl)-5- (trifluormethyl)-4H-1,2-oxazol-5-yl]carbonyl]amincoy]clopent-2-en-1- carboxylat, (B2.88) Methyl (4S)-4-[[[3-(3,5-difluorphenyl)-5-mtheyl-4H-1,2-oxazol-5- yl]carbonyl]amino]cyclopenten-1-carboxylat, (B2.89) Methyl (3S)-3-[[[(5R)-3-(3,5-difluorpheny-l5)-methyl-4H-1,2-oxazol-5- yl]carbonyl]amino]-cyclopenten-1-carboxylat, (B2.90) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4-(oxazin-a2-ylcarbonyl)cyclopent-2-en- 1-yl]-5-(trifluormethyl)-4H-1,2-oxazol-5-carboxam,id (B2.91) 3-(3,5-Difluorphenyl)-N-[(1R,4S)-4- [(propylsulfonylamino)carbonyl]cyclopent-2-en-1--y5l]-(trifluormethyl)-4H- 1,2-oxazol-5-carboxamid, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl-)[-(3S)-methylsulfinyl]-4- (trifluormethyl)benzamid, (B3.1) Bromoxynil, (B3.4) Ioxynil, (B4.8) Carfentrazone, (B4.11) Imazamox, (B4.13) Imazapyr, (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen,. BCS231024-Ausland STR 237 (B4.22) Pyrasulfotole, (B4.25) Pyroxasulfone,(B4.26) Sulfentrazone, (B4.27) Tolpyralate, (B5.5) Bentazone, (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.30) Fluthiacet- methyl, (B5.31) Halauxifen, (B5.37) Paraquat, (B5.38) Pelargonsäure, (B5.39) Pendimethalin, (B5.55) MSMA, (B6.3) Dicamba, (B7.4) Glufosinate, (B7.5) Glyphosate, (B7.7) Sulfosate, (B8.1) 2,4-D, (B8.2) 2,4-DB, (B8.3) 2,4-DP, (B8.4) Acifluorfen, (B8.5) Aclonifen, (B8.16) Fomesafen, (B8.19) Lactofen, (B8.24) Oxyfluorfen, (B9.3) Butafenacil, (B9.9) Pyrithiobac-sodium, (B9.10) Saflufenacil, (B9.11) Terbacil, (B9.12) Tiafenacil, BCS231024-Ausland STR 238 (B9.13) Trifludimoxazine, (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6-trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]acetate (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylate (B9.16) 3-[2-Chloro-5-(3,5-dimethyl-2,6- dioxo-4-sulfanyliden-1,3,5-triazinan- 1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6- dihydropyrimidin-1(2H)-yl]benzyliden}amino]oxy}propanoate, (B9.18) Flufenoximacil, (B10.5) Diuron, (B10.7) Fluometuron, (B10.8) Isoproturon, (B11.2) Atrazine, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.15) Terbuthylazine corresponds.

6. Composition according to one of the preceding claims, wherein (B) is selected from the group consisting of BCS231024-Ausland STR 239 (B1.2) Bicyclopyrone, (B1.4) Clethodim, (B1.7) Mesotrione, (B1.14) Tembotrione, (B2.1) Acetochlor, (B2.18) Diflufenican, (B2.20) Dimethenamid, (B2.28) Flufenacet, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.48) Phenmedipham, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.81) Icafolin-methyl, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl)-[-(3S)- methylsulfinyl]-4-(trifluormethyl)benzamid, (B3.1) Bromoxynil, (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, (B4.25) Pyroxasulfone, (B4.26) Sulfentrazone, (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.37) Paraquat, (B5.39) Pendimethalin, (B6.3) Dicamba, (B7.4) Glufosinate, (B7.5) Glyphosate, (B8.1) 2,4-D, (B8.5) Aclonifen, (B8.16) Fomesafen, (B8.24) Oxyfluorfen, BCS231024-Ausland STR 240 (B9.3) Butafenacil, (B9.10) Saflufenacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazine, (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6- trifluoromethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidin-3-yl)phenoxy]-2-pyridyloxy]aceta,t (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxyla,t (B9.16) 3-[2-Chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]-5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzylidene}amino]oxy}propanoa,t (B9.18) Flufenoximacil, (B10.5) Diuron, (B10.7) Fluometuron, (B11.2) Atrazine, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.15) Terbuthylazine.

7. Composition according to one of the preceding claims, wherein (B) is selected from the group consisting of (B1.2) Bicyclopyrones, (B1.4) Clethodim, (B1.7) Mesotrione, (B1.14) Tembotrione, (B2.1) Acetochlor, (B2.18) Diflufenican,. BCS231024-Ausland STR 241 (B2.20) Dimethenamid, (B2.28) Flufenacet, (B2.31) Foramsulfuron, (B2.34) Iodosulfuron, (B2.37) Mesosulfuron, (B2.63) Rimsulfuron, (B2.64) S-metolachlor, (B2.68) Thiencarbazone, (B2.81) Icafolin-methyl, (B2.93) 2-Chlor-N-(5-methyl-1,3,4-oxadiazol-2-yl-)[-(3S)- methylsulfinyl]-4-(trifluormethyl)benzamid, (B3.1) Bromoxynil, (B4.15) Imazethapyr, (B4.18) Isoxaflutole, (B4.20) Oxadiazon, (B4.21) Pyraflufen, (B4.25) Pyroxasulfone, (B4.26) Sulfentrazone, (B5.23) Florpyrauxifen, (B5.26) Flumioxazin, (B5.37) Paraquat, (B5.39) Pendimethalin, (B6.3) Dicamba, (B7.4) Glufosinate, (B7.5) Glyphosate, (B8.1) 2,4-D, (B8.5) Aclonifen, (B8.16) Fomesafen, (B8.24) Oxyfluorfen, (B9.3) Butafenacil, (B9.10) Saflufenacil, (B9.12) Tiafenacil, (B9.13) Trifludimoxazin, (B9.14) Ethyl[3-[2-chloro-4-fluoro-5-(1-methyl-6- trifluoromethyl-2,4-dioxo-1,2,3,4- BCS231024-Ausland STR 242 tetrahydropyrimidin-3-yl)phenoxy]-2- pyridyloxy]aceta,t (B9.15) Ethyl-3-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4- (trifluoromethyl)-3,6-dihydropyrimidine-1(2H)- yl]phenyl}-5-methyl-4,5-dihydro-1,2-oxazol-5-carboxyla,t (B9.16) 3-[2-chloro-5-(3,5-dimethyl-2,6-dioxo-4-sulfanyliden-1,3,5-triazinan-1-yl)-4-fluorophenyl]- 5-methyl-4,5-dihydro-1,2-oxazole-5-carboxylic acid, (B9.17) Methyl-(2RS)-2-{[(E)-{2-chloro-4-fluoro-5-[3-methyl-2,6-dioxo-4-(trifluoromethyl)-3,6-dihydropyrimidin-1(2H)-yl]benzylidene}amino]oxy}propanoate, (B9.18) Flufenoximacil, (B10.5) Diuron, (B10.7) Fluometuron, (B11.2) Atrazine, (B11.6) Indaziflam, (B11.8) Metribuzin, (B11.15) Terbuthylazine.

8. A composition according to any one of claims 7 to 11, wherein the compounds (A) and (B) are present in a weight ratio of 1:100,000 to 300:1, preferably 1:15,000 to 1000:

1. 9.Composition according to one of claims 81, wherein one or more further components from the group comprising plant-based active ingredients of a different type are present; and / or one or more additives are present in the plant-based active ingredient group.

10. Verfahren zur Bekämpfung von Schadpflanzenr z oudre Wachstumsregulierung von Pflanzen, wherein the compounds of the composition according to claims 1 to 9 are applied to the plants, plant parts, plant seeds or on the bulbs. BCS231024-Ausland STR 243 11. The method according to claim 10, wherein the compounds of the herbicidal composition are applied together or separately pre-emergence, post-emergence, or pre- and post-emergence to the plants, plant parts, plant seeds or bulbs.

12. The method according to claim 11, wherein the compound (A) is applied at an application rate of 0.02 to 250 g ai / ha; and / or wherein the compound (B) is applied at an application rate of 0 ,01 bis 4000 g a.i. / ha appliziert wird, ausgenomnm Pe largonsäure, die in einerApplication rate of 1 to 100,000 g ai / ha.

13. Method according to one of claims 10 to 12, for controlling weeds by treatment before sowing of the crops and in plant crops, as well as non-cultivated land.

14. Method according to one of claims 10 to 12, wherein the compounds of the composition are in the form of a herbicidal agent comprising one or more flanzenschutz übliche Zusatzstoffe enthält, genge nbfealls nach Verdünnen mit Wasser, be applied.

15. Verwendung der Zusammensetzung gemäß eine Amn dsepr üche 1 bis 9 zur Bekämpfung von harmful plants or to regulate the growth of plants.

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