The present invention is directed to an agricultural composition comprising a protoporphyrinogen oxidase (PPO) inhibitor, one or more sugar alcohols and optionally, one or more auxin herbicides. The present invention is further directed to a method of controlling weeds comprising applying concurrently or sequentially a PPO inhibitor and one or more sugar alcohols, and optionally one or more auxin herbicides to the weeds or an area in need of weed control.

The present invention is directed to an agricultural composition comprising a protoporphyrinogen oxidase (PPO) inhibitor, one or more sugar alcohols and optionally, one or more auxin herbicides. The present invention is further directed to a method of controlling weeds comprising applying concurrently or sequentially a PPO inhibitor and one or more sugar alcohols, and optionally one or more auxin herbicides to the weeds or an area in need of weed control.

The present invention is directed to pesticidal compositions comprising a pesticide, one or more acidifiers and one or more antagonists of the pesticide. The present invention is further directed to methods of controlling weeds by mixing pesticidal compositions comprising a pesticide and one or more acidifiers with one or more antagonists of the pesticide to create a tank mix and applying the tank mix to the weeds or an area in need of weed control.

The present invention is directed to pesticidal compositions comprising a pesticide, one or more acidifiers and one or more antagonists of the pesticide. The present invention is further directed to methods of controlling weeds by mixing pesticidal compositions comprising a pesticide and one or more acidifiers with one or more antagonists of the pesticide to create a tank mix and applying the tank mix to the weeds or an area in need of weed control.

A combination including a dithiocarbamate fungicide, a succinate dehydrogenase fungicide and at least one of ergosterol biosynthesis inhibitor fungicide or a quinone outside inhibitor fungicide.

A combination including a dithiocarbamate fungicide, a succinate dehydrogenase fungicide and at least one of ergosterol biosynthesis inhibitor fungicide or a quinone outside inhibitor fungicide.

A combination including a dithiocarbamate fungicide, a succinate dehydrogenase fungicide and at least one of ergosterol biosynthesis inhibitor fungicide or a quinone outside inhibitor fungicide.

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I ##STR00001## wherein R is hydrogen or methoxy; Q is ##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NO—C.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or —≡—R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I ##STR00001## wherein R is hydrogen or methoxy; Q is ##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NO—C.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or —≡—R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.

A method of controlling phytopathogenic diseases on useful plants or on propagation material thereof, which comprises applying to the useful plants, the locus thereof or propagation material thereof a combination of components (A) and (B) in a synergistically effective amount, wherein component (A) is a compound of formula I compound of formula I ##STR00001## wherein R is hydrogen or methoxy; Q is ##STR00002## R.sub.1 is hydrogen, halogen or C.sub.1-C.sub.6alkyl; R.sub.2 is hydrogen, halogen, C.sub.1-C.sub.6alkyl, C.sub.2-C.sub.6alkenyl, C.sub.3-C.sub.6alkinyl, C.sub.3-C.sub.6cycloalkyl-C.sub.3-C.sub.6alkinyl, halophenoxy, halophenyl-C.sub.3-C.sub.6alkinyl, C(C.sub.1-C.sub.4alkyl)=NO—C.sub.1-C.sub.4alkyl, C.sub.1-C.sub.6haloalkyl, C.sub.1-C.sub.6haloalkoxy, C.sub.2-C.sub.6haloalkenyl, or C.sub.2-C.sub.6haloalkenyloxy; R.sub.3 is hydrogen, halogen, C.sub.1-C.sub.6alkyl; R.sub.4, R.sub.5 and R.sub.6, independently from each other, are hydrogen, halogen or —≡—R.sub.7; with the proviso that at least one of R.sub.4, R.sub.5 and R.sub.6 is different from hydrogen; R.sub.7 is hydrogen, C.sub.1-C.sub.6alkyl, C.sub.1-C.sub.6haloalkyl or C.sub.1-C.sub.4alkoxyalkyl; and R.sub.8 is hydrogen or methoxy; and agrochemically acceptable salts/isomers/structural isomers/stereoisomers/diastereoisomers/enantiomers/tautomers and N-oxides of those compounds; and component (B) is a compound selected from compounds known for their fungicidal and/or insecticidal activity, is particularly effective in controlling or preventing fungal diseases of useful plants.