WO2014019983A1 - Compositions comprising a pesticidal terpene mixture and an insecticide - Google Patents

Compositions comprising a pesticidal terpene mixture and an insecticide Download PDF

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Publication number
WO2014019983A1
WO2014019983A1 PCT/EP2013/065905 EP2013065905W WO2014019983A1 WO 2014019983 A1 WO2014019983 A1 WO 2014019983A1 EP 2013065905 W EP2013065905 W EP 2013065905W WO 2014019983 A1 WO2014019983 A1 WO 2014019983A1
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WO
WIPO (PCT)
Prior art keywords
methyl
spp
carboxamide
trifluoromethyl
pyrazole
Prior art date
Application number
PCT/EP2013/065905
Other languages
French (fr)
Inventor
Elke Hellwege
Wolfram Andersch
Original Assignee
Bayer Cropscience Ag
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to JP2015524752A priority Critical patent/JP2015528017A/en
Application filed by Bayer Cropscience Ag filed Critical Bayer Cropscience Ag
Priority to CA2880369A priority patent/CA2880369C/en
Priority to US14/418,190 priority patent/US20150296773A1/en
Priority to MX2015001456A priority patent/MX2015001456A/en
Priority to BR112015002176A priority patent/BR112015002176A2/en
Priority to AU2013298625A priority patent/AU2013298625A1/en
Priority to EP13742230.9A priority patent/EP2879493B1/en
Priority to ES13742230T priority patent/ES2702303T3/en
Priority to KR20157002330A priority patent/KR20150040280A/en
Priority to CN201380045793.2A priority patent/CN104602520A/en
Priority to EP18181442.7A priority patent/EP3424322A1/en
Publication of WO2014019983A1 publication Critical patent/WO2014019983A1/en
Priority to ZA2015/00030A priority patent/ZA201500030B/en

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N27/00—Biocides, pest repellants or attractants, or plant growth regulators containing hydrocarbons
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
    • A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
    • A01N41/10—Sulfones; Sulfoxides
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
    • A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
    • A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N45/00—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring
    • A01N45/02—Biocides, pest repellants or attractants, or plant growth regulators, containing compounds having three or more carbocyclic rings condensed among themselves, at least one ring not being a six-membered ring having three carbocyclic rings
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
    • A01N47/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom containing —O—CO—O— groups; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/22—O-Aryl or S-Aryl esters thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
    • A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
    • A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
    • A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N51/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds having the sequences of atoms O—N—S, X—O—S, N—N—S, O—N—N or O-halogen, regardless of the number of bonds each atom has and with no atom of these sequences forming part of a heterocyclic ring
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof

Definitions

  • compositions comprising a pesticidal terpene mixture and an insecticide
  • the present invention relates to a composition
  • a composition comprising a pesticidal terpene mixture and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical.
  • the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.
  • Synthetic insecticides or fungicides often are non-specific and therefore can act on organisms other than the target ones, including other naturally occurring beneficial organisms. Because of their chemical nature, they may be also toxic and non-biodegradable. Consumers worldwide are increasingly conscious of the potential environmental and health problems associated with the residuals of chemicals, particularly in food products. This has resulted in growing consumer pressure to reduce the use or at least the quantity of chemical (i. e. synthetic) pesticides. Thus, there is a need to manage food chain requirements while still allowing effective pest control.
  • a further problem arising with the use of synthetic insecticides or fungicides is that the repeated and exclusive application of an insecticide or fungicides often leads to selection of resistant microorganisms. Normally, such strains are also cross-resistant against other active ingredients having the same mode of action. An effective control of the pests and pathogens with said active ingredients is then not possible any longer. However, active ingredients having new mechanisms of action are difficult and expensive to develop.
  • Natural insecticides are one approach for solving the above-mentioned problems. However, they are stille not entirely satisfactory.
  • a known simulated natural pesticide is Requiem®, which contains a mixture of three terpenes, i.e. a- terpinene, p-cymene and limonene, as pesticidally active ingredients. It is disclosed in US 2010/0316738 corresponding to WO 2010/144919 and the references cited therein, which are incorporated herein by reference. WO 20120/144919 also discloses the use of the terpene mixture disclosed in this document in combination with one or more additional pesticidally active ingredients against plant pests, such as a carrier, a solvent or another pesticide such as another insecticide or biopesticide.
  • Examples for additional pesticides which are disclosed in the document are fungicides, insecticides, miticides or acaricides, bactericides and the like as well as combinations thereof.
  • the use of extracts comprising these three terpenes obtained from Chenopodium ambrosioides for controlling insect or mite infestation on plants is kown, including the use of such extracts that include natural terpenes isolated form Chenopodium. See e.g.
  • compositions which exhibit activity against insects, mites, nematodes and/or phytopathogens were provided.
  • it was a further particular object of the present invention to reduce the application rates and broaden the activity spectrum of the natural and synthetic insecticides, and thereby to provide a composition which, preferably at a reduced total amount of active ingredients applied, has improved activity against insects, mites, nematodes and/or phytopathogens.
  • compositions according to the invention preferably fulfills the above-described needs. It has been surprisingly discovered that the application of the composition according to the present invention in a simultaneous or sequential way to plants, plant parts, harvested fruits, vegetables and/or plant's locus of growth preferably allows better control of insects, mites, nematodes and/or phytopathogens than it is possible with the pesticidal terpene mixture on the one hand and with the individual synthetic insecticides on the other hand, alone (synergistic mixtures). By applying the pesticidal terpene mixture and the at least one insecticide according to the invention the activity against insects, mites, nematodes and/or phytopathogens is peferably increased in a superadditive manner.
  • the composition according to the present invention preferably allows a reduced total amount of active ingredients to be used and thus the crops which have been treated by this composition preferably show a decreased amount of residues in the crop. Accordingly, the risk of resistance formation of harmful microorganisms is decreased.
  • the present invention is directed to a composition
  • a pesticidal terpene mixture comprising the three terpenes a-terpinene, p-cymene and limonene, and optionally minor terpene ingredients and impurities, which are e.g. found in essential oil extracts from Chenopodium ambrosioides near ambrosioides such as thymol, carvacrol, carvone, carveol, and/or nerol, and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical.
  • the present invention relates to a kit of parts comprising the pesticidal terpene mixture comprising the three terpenes as mentioned before and at least one insecticde.
  • the present invention is further directed to the use of said composition for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens.
  • the present invention provides a method for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens.
  • Pesticidal terpene mixture Pesticidal terpene mixture
  • a "pesticidal” means the ability of a substance to increase mortality or inhibit the growth rate of plant pests.
  • the term is used herein, to describe the property of a substance to exhibit activity against insects, mites, nematodes and/or phytopathogens.
  • the term "pests” include insects, mites, nematodes and/or phytopathogens.
  • the pesticidal terpene mixture of the invention comprises, as essential components, the terpenes a- terpinene, p-cymene and limonene.
  • the pesticidal mixture according to the invention may be obtained from any source such as, for example, as an extract from Chenopodium ambrosioides near ambrosioides, or as an extract from another plant genus/species that produces such terpenes, or produced synthetically (i.e. by a chemical synthesis process), and/or as a compound produced naturally by any organism (i.e. as a compound separate from an extract per se).
  • the three terpenes may be from natural extracts obtained from Chenopodium ambrosioides near ambrosioides, or they are from natural analogs of such terpenes as extract from other plant species or other organisms.
  • the terpenes may all three be synthetic versions of the terpenes obtainable from Chenopodium ambrosioides near ambrosioides or other plant species or other organisms. They may further be any possible combination of natural and/or synthetic versions of the three terpenes. Finally, the three terpenes can be obtained from any source or by any means except from an extract of Chenopodium ambrosioides near ambrosioides. Limonene exists in two enantiomeric forms, d- and 1-limonene, which are both included in the invention.
  • the pesticidal terpene mixture of the invention may, in a preferable embodiment, include only the essential oil extracts from or based on those found in Chenopodium ambrosioides near ambrosioides. It may aslo include only a synthetic blend simulating the essential oil extract from or based on those found in Chenopodium ambrosioides near ambrosioides. Further, it may include a mixture of the essential oil extract and the synthetic blend. It may be "normalized” by adding specific amounts of synthetic versions of one or more of the terpene compounds found in the natural extract and/or synthetic terpenes so as to produce a composition with a set ratio of the three terpenes.
  • the pesticidal terpene mixture of the invention comprises the three substantially pure terpenes a-terpinene, p-cymene and limonene.
  • the pesticidal terpene mixture does not contain thymol, carvacrol, carvone, carveol (cis and trans), nerol and/or ⁇ -terpinene, which are present in the extract from Chenopodium ambrosioides near ambrosioides at low levels.
  • the pesticidal terpene mixture does not contain said five terpenes and does not contain any other essential oils except those other essential oils that are present as minor impurities in the substantially pure a- terpinene, p-cymene and limonene. In the most preferred embodiment the pesticidal terpene mixture does not contain essential oils other than a-terpinene, p-cymene and limonene.
  • the pesticidal terpene mixture of the invention does not comprise the bicyclic monoterpene ascaridole due to the mammalian toxicity of this compound which can be present in natural extracts from Chenopodium ambrosioides depending on the cultivar and the growing conditions.
  • the simulated blends in the above compositions are not from an extract of Chenopodium ambrosioides or from an extract of Chenopodium.
  • the pesticidally active compositions of the present invention only include the essential oil extracts from or based on those found in Chenopodium ambrosioides near ambrosioides.
  • the pesticidally active compositions ofthe present invention only include a synthetic blend simulating the essential oil extract from or based on those found in Chenopodium ambrosioides near ambrosioides.
  • the pesticidally active compositions of the present invention include a mixture of the essential oil extract and the synthetic blend.
  • compositions to be applied to plants as a protectant are "normalized” by adding specific amounts of synthetic versions of one or more of the terpene compounds found in the natural extract and/or synthetic terpenes so as to produce a composition with a set ratio of the three terpenes, such as the ratio observed in certain standardized or preferred natural extracts from or based on those found in Chenopodium.
  • compositions used in the methods of the present invention are reconstituted, as explained more herein.
  • the simulated blends simulating the Chenopodium extract consist essentially of natural analogs of such terpenes trom other plant species or other organisms, and/or the synthetic versions of such terpenes.
  • simulated blends comprise the three substantially pure ⁇ -terpinene, p-cymene and limonene, optionally with at least one volume filler that replaces the volume taken up by the minor components normally present in the extract of Chenopodium ambrosioides near ambrosioides.
  • the simulated blends consist essentially of a-terpinene, p-cymene and limonene, and an oil wherein the a-terpinene, p-cymene and limonene are substantially pure and are not obtained from a Chenopodium extract, and wherein the excipient is not an essential oil.
  • the limonene is prepared from citrus peels or pines by cold press method.
  • the concentration of the ⁇ -terpinene in the pesticidal terpene mixture of the invention ranges from about 30 to about 70 %, preferably 35 % to 45 % and most preferably about 39 % by weight
  • the concentration of p-cymene in the pesticidal terpene mixture ranges from about 10 % to about 30 %, preferably from about 15 % to about 25 % and most preferably about 17 % by weight
  • the concentration of limonene in the pesticidal terpene mixture ranges from about 1 % to about 20 %, preferably from about 5 % to about 15 % by weight and most preferably about 12 %, all based on the terpene mixture.
  • the absolute concentrations of ⁇ -terpinene is about 36 %, that of p-cymene is about 14.9 % and that of limonene is about 11.4 % by weight, all based on the pesticidal terpene mixture.
  • the relative ratio of ⁇ -terpinene, p-cymene and limonene in the pesticidal terpene mixture is 35-45 ⁇ -terpinene to about 12-20 p-cymene to about 10-15 limonene.
  • Examples for preferable relative ratios of ⁇ -terpinene, p-cymene and limonene are 39: 17: 12, or about 40:15: 12, or about 36: 14.9: 11.4, or about 10.175:3.9:3.05.
  • the concentration of substantially pure ⁇ -terpinene in the compositions is about 39% by weight; the concentration of substantially pure p-cymene in the compositions is about 17% by weight, and the concentration of substantially pure limonene in the compositions is about 12%> by weight.
  • the concentration of each pesticidally active terpene can be higher or lower than in the essential oil extract from Chenopodium ambrosioides near ambrosioides, but roughly maintaining the relative ratio to each others as in the essential oil extract.
  • the pesticidal terpene mixture of the invention can be obtained as an extract from Chenopodium ambrosioides near ambrosoides, as described in US 2009/0091657 and US 2009/0030087 as well as WO 2001/067868 and WO 2004/006679. It is also described in detail in US 61/213,470, US 61/246,872, US 61/247,885, US 61/256,257, US 61/286,314 and US 61/329,020, and it can be obtained as disclosed in US 2010/0316738 corresponding to WO 2012/14419. The disclosure of these documents is incorporated herein by reference.
  • ⁇ -Terpinene, p-cymene and limonene are publicly available, can be produced synthetically using known methods or can be purified from various plant extracts according to methods generally known in the art. Further, all three of the terpenes are commercially available (e.g. Sigma- Aldrich®, Acros Organics, MP Biomedicals, Merck Chemicals). At least the following plant species produce a-terpinene: Anethum graceolens, Artemisia argyi, Cuminum cyminum, Elattaria cardamonum, Melaleuca alternifolia, Cardamom spp. and Origanum major ana.
  • At least the following plant species produce limonene, including d-limonene: Anethum graceolens, Anethum sowa, Carum carvi, Citrus, Foeniculum vulgare, Mentha piperita and Peppermint. Limonene may be obtained by steam distillation after alkali treatment of citrus peels and pulp, and also by fractionation of orange oil.
  • At least the following plant species produce p-cymene Coridothymus sativum, Coridothymus captitatus, Cuminum cyminum, Origanum vulgare and Thymus vulgaris. Additional plants that produce the three terpenes are known in the art. Essential oils and/or certain fractions of essential oils (e.g. certain terpenes) can be extracted from a plant by distillation.
  • Essential oils means the volatile, aromatic oils obtained by steam or hydrodestillation of plant material and may include, but are not restricted to, being primarily composed of terpenes and their oxygenated derivatives.
  • Essential oils can be obtained from, for example, flowers, leaves, seeds, roots, stems, bark, wood etc. Extraction and distillation methods of essential oils are known in the art.
  • a particularly preferable pesticidal terpene mixture of the invention is commercially available from the company AgroQuest under the trade name Requiem®.
  • this commercial product is used as pesticidal terpene mixture according to the invention.
  • Requiem® contains excipients, solvents and other ingredients.
  • all amounts of the "pesticidal terpene mixture of the invention" mentioned in commection with Requiem® refer to the amount of the three terpenes contained in Requiem®, and not to the amount of the complete product Requiem®.
  • insects as well as the term “insecticidal” refers to the ability of a substance to increase mortality or inhibit growth rate of insects. As used herein, the term “insects” includes all organisms in the class “Insecta”. The term “pre-adult” insects refers to any form of an organism prior to the adult stage, including, for example, eggs, larvae, and nymphs.
  • nematodes and “nematicidal” refers to the ability of a substance to increase mortality or inhibit the growth rate of nematodes.
  • nematode comprises eggs, larvae, juvenile and mature forms of said organism.
  • Acaricide and “acaricidal” refers to the ability of a substance to increase mortality or inhibit growth rate of ectoparasites belonging to the class Arachnida, sub-class Acari.
  • insecticides specified herein by their "common name” are known and described, for example, in the Pesticide Manual ("The Pesticide Manual", 15th Ed., British Crop Protection Council 2009) or can be searched in the internet (e.g. http://www.alanwood.net/pesticides).
  • Acetylcholinesterase (AChE) inhibitors for example carbamates, e.g. Alanycarb (II), Aldicarb (12), Bendiocarb (13), Benfuracarb (14), Butocarboxim (15), Butoxycarboxim (16), Carbaryl (17), Carbofuran (18), Carbosulfan (19), Ethiofencarb (110), Fenobucarb (111), Formetanate (112), Furathiocarb (113), Isoprocarb (114), Methiocarb (115), Methomyl (116), Metolcarb (117), Oxamyl (118), Pirimicarb (119), Propoxur (120), Thiodicarb (121), Thiofanox (122), Triazamate (123), Trimethacarb (124), XMC (125), and Xylylcarb (126); or organophosphates, e.g.
  • GABA-gated chloride channel antagonists for example cyclodiene organochlorines, e.g. Chlordane (192) and Endosulfan (193); or phenylpyrazoles (fiproles), e.g. Ethiprole (194) and Fipronil (195);
  • Sodium channel modulators / voltage-dependent sodium channel blockers for example pyrethroids, e.g. Acrinathrin (196), Allethrin (197), d-cis-trans Allethrin (198), d-trans Allethrin (199), Bifenthrin
  • Nicotinic acetylcholine receptor (nAChR) agonists for example neonicotinoids, e.g. Acetamiprid (1141), Clothianidin (1142), Dinotefuran (1143), Imidacloprid (1144), Nitenpyram (1145), and Thiacloprid (1146), and Thiamethoxam (1147); or Nicotine (1148); or Sulfoxaflor (1149).
  • neonicotinoids e.g. Acetamiprid (1141), Clothianidin (1142), Dinotefuran (1143), Imidacloprid (1144), Nitenpyram (1145), and Thiacloprid (1146), and Thiamethoxam (1147); or Nicotine (1148); or Sulfoxaflor (1149).
  • Nicotinic acetylcholine receptor (nAChR) allosteric activators for example spinosyns, e.g. Spinetoram (1150) and Spinosad (1151);
  • Chloride channel activators for example avermectins/milbemycins, e.g. Abamectin (1152), Emamectin benzoate (1153), Lepimectin (1154), and Milbemectin (1155);
  • avermectins/milbemycins e.g. Abamectin (1152), Emamectin benzoate (1153), Lepimectin (1154), and Milbemectin (1155);
  • Juvenile hormone mimics for example juvenile hormon analogues, e.g. Hydroprene (1156), Kinoprene (1157), and Methoprene (1158); or Fenoxycarb (1159); or Pyriproxyfen (1160); (8) Miscellaneous non-specific (multi-site) inhibitors, for example alkyl halides, e.g. Methyl bromide (1161) and other alkyl halides; or Chloropicrin (1162); or Sulfuryl fluoride (1163); or Borax (1164); or Tartar emetic (1165);
  • alkyl halides e.g. Methyl bromide (1161) and other alkyl halides; or Chloropicrin (1162); or Sulfuryl fluoride (1163); or Borax (1164); or Tartar emetic (1165);
  • Mite growth inhibitors e.g. Clofentezine (1168), Hexythiazox (1169), and Diflovidazin (1170); or Etoxazole (I171); - -
  • Microbial disruptors of insect midgut membranes e.g. Bacillus thuringiensis subspecies israelensis (1172), Bacillus thuringiensis subspecies aizawai (1173), Bacillus thuringiensis subspecies kurstaki (1174), Bacillus thuringiensis subspecies tenebrionis (1175), and B.t. Microbial disruptors of insect midgut membranes, e.g. B.t.
  • crop proteins CrylAb, CrylAc, CrylFa, CrylA.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, Cry34 Abl/35Abl (1176); or Bacillus sphaericus (1177);
  • Inhibitors of mitochondrial ATP synthase for example Diafenthiuron (1178); or organotin miticides, e.g. Azocyclotin (1179), Cyhexatin (1180), and Fenbutatin oxide (1181); or Propargite (1182); or Tetradifon (1183);
  • Nicotinic acetylcholine receptor (nAChR) channel blockers for example Bensultap (1187), Cartap hydrochloride (1188), Thiocyclam (1189), and Thiosultap-sodium (1190);
  • Inhibitors of chitin biosynthesis type 0, for example Bistrifluron (1191), Chlorfluazuron (1192), Diflubenzuron (1193), Flucycloxuron (1194), Flufenoxuron (1195), Hexaflumuron (1196), Lufenuron (1197), Novaluron (1198), Noviflumuron (1199), Teflubenzuron (1200), and Triflumuron (1201);
  • Inhibitors of chitin biosynthesis type 1, for example Buprofezin (1202);
  • Moulting disruptors for example Cyromazine (1203);
  • Ecdysone receptor agonists for example Chromafenozide (1204), Halofenozide (1205), Methoxyfenozide (1206), and Tebufenozide (1207);
  • Octopamine receptor agonists for example Amitraz (1208);
  • Mitochondrial complex III electron transport inhibitors for example Hydramethylnon (1209); or Acequinocyl (1210); or Fluacrypyrim (1211);
  • METI acaricides e.g. Fenazaquin (1212), Fenpyroximate (1213), Pyrimidifen (1214), Pyridaben (1215), Tebufenpyrad (1216), and Tolfenpyrad (1217); or Rotenone (Derris) (1218);
  • Inhibitors of acetyl CoA carboxylase for example tetronic and tetramic acid derivatives, e.g. Spirodiclofen (1221), Spiromesifen (1222), and Spirotetramat (1223); - -
  • Mitochondrial complex IV electron transport inhibitors for example phosphines, e.g. Aluminium phosphide (1224), Calcium phosphide (1225), Phosphine (1226), and Zinc phosphide (1227); or Cyanide (1228);
  • phosphines e.g. Aluminium phosphide (1224), Calcium phosphide (1225), Phosphine (1226), and Zinc phosphide (1227); or Cyanide (1228);
  • Mitochondrial complex II electron transport inhibitors for example beta-ketonitrile derivatives, e.g. Cyenopyrafen (1229) and Cyflumetofen (1230);
  • Ryanodine receptor modulators for example diamides, e.g. Chlorantraniliprole (1231), Cyantraniliprole (1232), and Flubendiamide (1233);
  • the insecticide is a synthetic insecticide.
  • synthetic defines a compound that has not been obtained from a natural source such as a plant, bacterium or other organism.
  • the insecticide is selected from the group consisting of Abamectin (1152) , Acephate (127), Acetamiprid (1141), Acrinathrin (196), Afidopyropen (1278), Alpha-Cypermethrin (II 11), Azadirachtin (1235), Bacillus firmus (1256), (Beta-Cyfluthrin (1106), Bifenthrin (1100), Buprofezin (1202), Clothianidin (1142), Chlorantraniliprole (1231), Chlorfenapyr (1184), Chlorpyrifos (135), Carbofuran (18), Cyantraniliprole (1232), Cyenopyrafen (1229), Cyflumentofen (1230), Cyfluthrin (1105), Cypermethrin (1110), Deltamethrin (1116), Diafenthiuron (1178), Dinotefuran (1143), Emamectin-benzoate (1153), E
  • the insecticide b) is selected from the group consisting of Abamectin (1152), Beta-Cyfluthrin (1-105), Clothianidin (1142), Chlorantraniliprole (1231), Cyantraniliprole (1232), Deltamethrin (1116), Fipronil (195), Flubendiamide (1233), Flupyradifurone (1262), Imidacloprid (1144), Methiocarb (1115), Sulfoxaflor (I149)Spinetoram (1150), Spinosad (1151), Spiromesifen (1222), Spirotetramate (1223), Tefluthrin (1134), Thiacloprid (1146), Thiamethoxam (1147), Thiodicarb (121), a mixture of l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- ⁇ [5- (triflufluorin
  • the insecticide e.g. for seed treatment, is selected from the group consisting of Abamectin (1152), Carbofuran (18), Clothianidin (1142), Cyazypyr , Cycloxaprid, Cypermethrin (1110), Ethiprole (194), Fipronil (195), Fluopyram (1247), Imidacloprid (1144), Methiocarb (115), Rynaxypyr, Spinosad (1151), Sulfoxaflor (1149), Tefluthrin (1134), Thiametoxam (1147),
  • the composition comprises two or more insecticides.
  • the composition comprises two or more of the above-mentioned preferred insecticides.
  • the preferred two or more insecticides are selected from the group consisting of Abamectin (1152) , Acephate (127), Acetamiprid (1141), Acrinathrin (196), Afidopyropen (1278), Alpha-Cypermethrin (1111), Azadirachtin (1235), Bacillus firmus, Beta-Cyfluthrin (1106), Bifenthrin (1100), Buprofezin (1202), Clothianidin (1142), Chlorantraniliprole (1231), Chlorfenapyr (1184), Chlorpyrifos (135), Carbofuran (18), Cyantraniliprole (1232), Cyenopyrafen (1229), Cyflumentofen (1230), Cyfluthrin (1105), Cypermethrin (1110), Deltamethrin (1
  • compositions according to the present invention are provided.
  • the composition comprises the pesticidal terpene mixture as defined above and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical.
  • a “synergistically effective amount” represents a quantitiy of a combination of the pesticidal terpene mixture and an insecticide that is statistically significantly more effective against insects, mites, nematodes and/or phytopatheogens than the pesticidal terpene mixture or the insecticide alone.
  • X is the efficacy expressed in % mortality of the untreated control for test compound A at a concentration of m ppm respectively m g/ha.
  • Y is the efficacy expressed in % mortality of the untreated control for test compound B at a concentration of n ppm respectively n g/ha. 5
  • E is the efficacy expressed in % mortality of the untreated control using the mixture
  • the combination of the two compounds is more than additive, i.e., there is a synergistic effect.
  • composition according to the present invention comprises the following combinations:
  • Bl means the pesticidal terpene mixture according to the invention comprising a-terpinene, p-cymene and limonene as defined before.
  • the composition comprises Requiem® and an insecticide b) selected from the group consisting of Abamectin, Beta-Cyfluthrin, Clothianidin, Chlorantraniliprole, Cyantraniliprole, Deltamethrin, Fipronil, Flubendiamide, Flupyradifurone, Imidacloprid, Methiocarb, Spinetoram, Spinosad, Spiromesifen, Spirotetramate, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, a mixture of l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- ⁇ [5-(trifluoromethyl)- 2H-tetrazol-2-yl]methyl ⁇ -lH-pyrazole-5-carboxamide and l-(3-chloropyridin-2-
  • compositions of the inventions are not the following combinations: - Pesticidal terpene mixture and ⁇ , ⁇ -diethyl-toluamide (Autan®) ?
  • the sequential treatment in particular of watermelon seedlings, comprising separate treatment with the pesticidal terpene mixture of the invention and the specific insecticides/fungicides 2x Pymetrozine (Fulfill®), 2x Endosulfan (Thionex®), 2x Spiromesifen (Oberon®), 2x Endosulfan (Thionex®), as disclosed in Example 5 of WO 20120/144919,
  • WO 20120/144919 discloses combiantions of the pesticidal terpene mixture with 2-ethyl-l,3- hexanediol, N-octyl bicycloheptene dicarboxamide, N,N-diethyl-M-toluamide, 2,3:4,5-Bis (2-butylene) tetrahydro-2-furaldehyde, Di-n-propyl isocinchomeronate, 2-hydroxyethyl-n-octyl sulfide.
  • These compounds are described in WO 20120/144919 as "other repellents". However, the present inventors consider them merely formulation aids. Again, combinations of the pestcicidal terpene mixture with these compounds are excluded from the present invention.
  • the composition further comprises at least one fungicide with the proviso that the pesticidal terpene mixture and the fungicide are not identical.
  • active ingredient is used in the present description to designate the pestcidal terpene mixture, the insecticide and the fungicide.
  • fungicidal means the ability of a substance to increase mortality or inhibit the growth rate of fungi.
  • fungus or "fungi” includes a wide variety of nucleated sporebearing organisms that are devoid of chlorophyll. Examples of fungi include yeasts, molds, mildews, rusts, and mushrooms.
  • Inhibitors of the ergosterol biosynthesis for example (Fl) aldimorph (1704-28-5), (F2) azaconazole (60207-31-0), (F3) bitertanol (55179-31-2), (F4) bromuconazole (116255-48-2), (F5) cyproconazole (113096-99-4), (F6) diclobutrazole (75736-33-3), (F7) difenoconazole (119446-68-3), (F8) diniconazole (83657-24-3), (F9) diniconazole-M (83657-18-5), (F10) dodemorph (1593-77-7), (Fl l) dodemorph acetate (31717-87-0), (F12) epoxiconazole (106325-08-0), (F13) etaconazole (60207-93-4), (F14) fenarimol (60168-88-9), (F15) fenbuconazole (1143
  • inhibitors of the respiratory chain at complex I or II for example (F65) bixafen (581809-46-3), (F66) boscalid (188425-85-6), (F67) carboxin (5234-68-4), (F68) diflumetorim (130339-07-0), (F69) fenfuram (24691-80-3), (F70) fluopyram (658066-35-4), (F71) flutolanil (66332-96-5), (F72) fluxapyroxad (907204-31-3), (F73) furametpyr (123572-88-3), (F74) furmecyclox (60568-05-0), (F75) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR) (881685- 58-1), (F76) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR),
  • inhibitors of the respiratory chain at complex III for example (F105) ametoctradin (865318-97-4), (F106) amisulbrom (348635-87-0), (F107) azoxystrobin (131860-33-8), (F108) cyazofamid (120116-88- 3), (F109) coumethoxystrobin (850881-30-0), (F110) coumoxystrobin (850881-70-8), (Fi l l) dimoxystrobin (141600-52-4), (F112) enestroburin (238410-11-2), (F113) famoxadone (131807-57-3), - -
  • Inhibitors of the mitosis and cell division for example (F138) benomyl (17804-35-2), (F139) carbendazim (10605-21-7), (F140) chlorfenazole (3574-96-7), (F141) diethofencarb (87130-20-9), (F142) ethaboxam (162650-77-3), (F143) fluopicolide (239110-15-7), (F144) fuberidazole (3878-19-1), (F145) pencycuron (66063-05-6), (F146) thiabendazole (148-79-8), (F147) thiophanate-methyl (23564- 05-8), (F148) thiophanate (23564-06-9), (F149) zoxamide (156052-68-5), (F150) 5-chloro-7-(4- methylpiperidin-l-yl)-6-(2,4,6-trifluorophenyl)[l,2,4]triazolo[l,2,
  • Inhibitors of the amino acid and/or protein biosynthesis for example (F190) andoprim (23951 -85-1), (F191) blasticidin-S (2079-00-7), (F192) cyprodinil (121552-61-2), (F193) kasugamycin (6980-18-3), (F194) kasugamycin hydrochloride hydrate (19408-46-9), (F195) mepanipyrim (110235-47-7), (F196) pyrimethanil (53112-28-0), (F197) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-l- yl)quinoline (861647-32-7);
  • Inhibitors of the ATP production for example (F198) fentin acetate (900-95-8), (F199) fentin chloride (639-58-7), (F200) fentin hydroxide (76-87-9), (F201) silthiofam (175217-20-6); (9) Inhibitors of the cell wall synthesis, for example (F202) benthiavalicarb (177406-68-7), (F203) dimethomorph (110488-70-5), (F204) flumorph (211867-47-9), (F205) iprovalicarb (140923-17-7), (F206) mandipropamid (374726-62-2), (F207) polyoxins (11113-80-7), (F208) polyoxorim (22976-86- 9), (F209) validamycin A (37248-47-8), (F210) valifenalate (283159-94-4; 283159-90-0);
  • Inhibitors of the lipid and membrane synthesis for example (F211) biphenyl (92-52-4), (F212) chloroneb (2675-77-6), (F213) dicloran (99-30-9), (F214) edifenphos (17109-49-8), (F215) etridiazole (2593-15-9), (F216) iodocarb (55406-53-6), (F217) iprobenfos (26087-47-8), (F218) isoprothiolane (50512-35-1), (F219) propamocarb (25606-41-1), (F220) propamocarb hydrochloride (25606-41-1), (F221) prothiocarb (19622-08-3), (F222) pyrazophos (13457-18-6), (F223) quintozene (82-68-8), (F224) tecnazene (117-18-0), (F225) tolclofos-methyl (57018-04
  • Inhibitors of the nucleic acid synthesis for example (F233) benalaxyl (71626-11-4), (F234) benalaxyl-M (kiralaxyl) (98243-83-5), (F235) bupirimate (41483-43-6), (F236) clozylacon (67932-85- 8), (F237) dimethirimol (5221-53-4), (F238) ethirimol (23947-60-6), (F239) furalaxyl (57646-30-7), (F240) hymexazol (10004-44-1), (F241) metalaxyl (57837-19-1), (F242) metalaxyl-M (mefenoxam) - -
  • Inhibitors of the signal transduction for example (F246) chlozolinate (84332-86-5), (F247) fenpiclonil (74738-17-3), (F248) fludioxonil (131341-86-1), (F249) iprodione (36734-19-7), (F250) procymidone (32809-16-8), (F251) quinoxyfen (124495-18-7), (F252) vinclozolin (50471-44-8);
  • fungicides of the classes (1) to (16) can, if their functional groups enable this, optionally form salts with suitable bases or acids.
  • the at least fungicide is a synthetic fungicide.
  • the composition comprises two or more fungicides. In a preferred embodiment the composition comprises two or more of the above-mentioned preferred fungicides.
  • the fungicide is selected from the group consisting of (1) Inhibitors of the ergosterol biosynthesis, for example (F3) bitertanol, (F4) - 5 - bromuconazole (116255-48-2), (F5) cyproconazole (1 13096-99-4), (F7) difenoconazole (119446-68-3), (F12) epoxiconazole (106325-08-0), (F16) fenhexamid (126833-17-8), (F17) fenpropidin (67306-00-7), (F18) fenpropimorph (67306-03-0), (F19) fluquinconazole (136426-54-5), (F22) flutriafol, (F26) imazalil, (F29) ipconazole (125225-28-7), (F30) metconazole (125116-23-6), (F31) myclobutanil (88671-
  • inhibitors of the respiratory chain at complex I or II for example (F65) bixafen (581809-46-3), (F66) boscalid (188425-85-6), (F67) carboxin (5234-68-4), (F70) fluopyram (658066-35-4), (F71) flutolanil (66332-96-5), (F72) fluxapyroxad (907204-31-3), (F73) furametpyr (123572-88-3), (F75) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR) (881685- 58-1), (F76) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (F77) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (F78) isopyrazam (anti-epimeric enanti
  • Inhibitors of the mitosis and cell division for example (F139) carbendazim (10605-21-7), (F140) chlorfenazole (3574-96-7), (F141) diethofencarb (87130-20-9), (F142) ethaboxam (162650-77-3), (F143) fluopicolide, (F144) fuberidazole (3878-19-1), (F145) pencycuron (66063-05-6), (F147) thiophanate-methyl (23564-05-8), (F149) zoxamide (156052-68-5); - -
  • Inhibitors of the amino acid and/or protein biosynthesis for example (F192) cyprodinil (121552-61- 2), (F196) pyrimethanil (53112-28-0);
  • Inhibitors of the cell wall synthesis for example (F202) benthiavalicarb (177406-68-7), (F203) dimethomorph (110488-70-5), (F205) iprovalicarb (140923-17-7), (F206) mandipropamid (374726-62- 2), (F210) valifenalate (283159-94-4; 283159-90-0);
  • Inhibitors of the lipid and membrane synthesis for example (F216) iodocarb (55406-53-6), (F217) iprobenfos (26087-47-8), (F220) propamocarb hydrochloride (25606-41-1), (F225) tolclofos-methyl;
  • Inhibitors of the nucleic acid synthesis for example (F233) benalaxyl (71626-11-4), (F234) benalaxyl-M (kiralaxyl) (98243-83-5), (F239) furalaxyl (57646-30-7), (F240) hymexazol (10004-44-1), (F241) metalaxyl (57837-19-1), (F242) metalaxyl-M (mefenoxam) (70630-17-0), (F244) oxadixyl (77732-09-3);
  • Inhibitors of the signal transduction for example (F247) fenpiclonil (74738-17-3), (F248) fludioxonil (131341-86-1), (F249) iprodione (36734-19-7), (F251) quinoxyfen (124495-18-7), (F252) vinclozolin (50471-44-8);
  • the fungizide is selected from the group consisting of Carbendazim (F139), Carboxin (F67), Difenoconazole (F7), Fludioxonil (F248), Fluquinconazole (F19), - 7 -
  • Fluxapyroxad F72
  • Ipconazole F29
  • Isotianil F187
  • Mefenoxam F242
  • Metalaxyl F241
  • Pencycuron F145
  • Penflufen F84
  • Prothioconazole F41
  • Prochloraz F39
  • Pyraclostrobin F121
  • Sedaxane F86
  • Silthiofam F201
  • Tebuconazole F47
  • Thiram F182
  • Trifloxystrobin F126
  • Triticonazole F55
  • One aspect of the present invention is to provide a composition as described above additionally comprising at least one auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants.
  • auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants.
  • formulations are referred to as formulations.
  • such formulations, and application forms prepared from them are provided as crop protection agents and/or pesticidal agents, such as drench, drip and spray liquors, comprising the composition of the invention.
  • the application forms may comprise further crop protection agents and/or pesticidal agents, and/or activity- enhancing adjuvants such as penetrants, examples being vegetable oils such as, for example, rapeseed oil, sunflower oil, mineral oils such as, for example, liquid paraffins, alkyl esters of vegetable fatty acids, such as rapeseed oil or soybean oil methyl esters, or alkanol alkoxylates, and/or spreaders such as, for example, alkylsiloxanes and/or salts, examples being organic or inorganic ammonium or phosphonium salts, examples being ammonium sulphate or diammonium hydrogen phosphate, and/or retention promoters such as dioctyl sulphosuccinate or hydroxypropylgu
  • formulations include water-soluble liquids (SL), emulsifiable concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS); these and other possible types of formulation are described, for example, by Crop Life International and in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers - 173, prepared by the FAO/WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576.
  • the formulations may comprise active agrochemical compounds other than one or more active ingredients of the invention.
  • the formulations or application forms in question preferably comprise auxiliaries, such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, biocides, thickeners and/or other auxiliaries, such as adjuvants, for example.
  • auxiliaries such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, biocides, thickeners and/or other auxiliaries, such as adjuvants, for example.
  • An adjuvant in this context is a component which enhances the biological effect of the formulation, without the component itself having a biological effect.
  • adjuvants are agents which promote the retention, spreading, attachment to the leaf surface, or penetration.
  • formulations are produced in a known manner, for example by mixing the active ingredients with auxiliaries such as, for example, extenders, solvents and/or solid carriers and/or further auxiliaries, such as, for example, surfactants.
  • auxiliaries such as, for example, extenders, solvents and/or solid carriers and/or further auxiliaries, such as, for example, surfactants.
  • the formulations are prepared either in suitable plants or else before or during the application.
  • auxiliaries are substances which are suitable for imparting to the formulation of the active ingredient or the application forms prepared from these formulations (such as, e.g., usable crop protection agents, such as spray liquors or seed dressings) particular properties such as certain physical, technical and/or biological properties.
  • Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N- alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide).
  • aromatic and non-aromatic hydrocarbons such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes
  • the alcohols and polyols
  • suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulphoxide, and also water.
  • aromatics such as xylene, toluene or alkylnaphthalenes
  • chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride
  • aliphatic hydrocarbons
  • Suitable solvents are, for example, aromatic hydrocarbons, such as xylene, toluene or alkylnaphthalenes, for example, chlorinated aromatic or aliphatic hydrocarbons, such as chlorobenzene, chloroethylene or methylene chloride, for example, aliphatic hydrocarbons, such as cyclohexane, for example, paraffins, petroleum fractions, mineral and vegetable oils, alcohols, such as methanol, ethanol, isopropanol, butanol or glycol, for example, and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, for example, strongly polar solvents, such as dimethyl sulphoxide, and water.
  • aromatic hydrocarbons such as xylene, toluene or alkylnaphthalenes
  • chlorinated aromatic or aliphatic hydrocarbons such as chloro
  • Suitable carriers are in particular: for example, ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and/or solid fertilizers. Mixtures of such carriers may likewise be used.
  • Carriers suitable for granules include the following: for example, crushed and fractionated natural minerals such as calcite, marble, pumice, sepiolite, dolomite, and also synthetic granules of inorganic and organic meals, and also granules of organic material such as sawdust, paper, coconut shells, maize cobs and tobacco stalks.
  • Liquefied gaseous extenders or solvents may also be used. Particularly suitable are those extenders or carriers which at standard temperature and under standard pressure are gaseous, examples being aerosol propellants, such as halogenated hydrocarbons, and also butane, propane, nitrogen and carbon dioxide.
  • emulsifiers and/or foam-formers, dispersants or wetting agents having ionic or nonionic properties, or mixtures of these surface-active substances are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphomc acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyltaurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, examples being alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, protein hydrolyceride
  • auxiliaries that may be present in the formulations and in the application forms derived from them include colorants such as inorganic pigments, examples being iron oxide, titanium oxide, Prussian Blue, and organic dyes, such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and nutrients and trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
  • Stabilizers such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability may also be present. Additionally present may be foam-formers or defoamers.
  • formulations and application forms derived from them may also comprise, as additional auxiliaries, stickers such as carboxymethylcellulose, natural and synthetic polymers in powder, granule or latex form, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids.
  • additional auxiliaries include mineral and vegetable oils.
  • auxiliaries present in the formulations and the application forms derived from them.
  • additives include fragrances, protective colloids, binders, adhesives, thickeners, thixotropic substances, penetrants, retention promoters, stabilizers, sequestrants, complexing - - agents, humectants and spreaders.
  • the active ingredients may be combined with any solid or liquid additive commonly used for formulation purposes.
  • Suitable retention promoters include all those substances which reduce the dynamic surface tension, such as dioctyl sulphosuccinate, or increase the viscoelasticity, such as hydroxypropylguar polymers, for example.
  • Suitable penetrants in the present context include all those substances which are typically used in order to enhance the penetration of active agrochemical compounds into plants.
  • Penetrants in this context are defined in that, from the (generally aqueous) application liquor and/or from the spray coating, they are able to penetrate the cuticle of the plant and thereby increase the mobility of the active ingredients in the cuticle. This property can be determined using the method described in the literature (Baur et al., 1997, Pesticide Science 51, 131-152).
  • Examples include alcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed or soybean oil methyl esters, fatty amine alkoxylates such as tallowamine ethoxylate (15), or ammonium and/or phosphonium salts such as ammonium sulphate or diammonium hydrogen phosphate, for example.
  • the formulations preferably comprise between 0.0001% and 98% by weight of active ingredients or, with particular preference, between 0.01% and 95% by weight of active ingredients, more preferably between 0.5% and 90% by weight of active ingredient, based on the weight of the formulation.
  • the content of the active ingredients is defined as the sum of the pesticidal terpene mixture and the at least one insecticide and optionally the amount of fungicide.
  • the pestcidial terpene mixture means the mixture of the three terpenes a-terpinene, p-cymene and limonene as essential components and optionally impurities such as those contained in the extract of Chenopodium ambrosioi des near ambrosioides. If, e.g.
  • the commercial product Requiem® is used as pesticidal terpene mixture, the amount thereof is selected in such a way that the amount of the three pesticidal terpenes a-terpinene, p- cymene and limonene in total contained therein meets the requirements defined in the following. This definition applies throughout the following description as well.
  • the active ingredient content of the application forms (crop protection products) prepared from the formulations may vary within wide ranges.
  • the active ingredient concentration of the application forms may be situated typically between 0.0001%> and 95% by weight of active ingredient, preferably between 0.001%) and 1%> by weight, based on the weight of the application form.
  • Application takes place in a customary manner adapted to the application forms.
  • a kit of parts comprising the pesticidal terpene mixture and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical, in a spatially separated arrangement.
  • the above-mentioned kit of parts further comprises at least one fungicide, with the proviso that the pesticidal terpene mixture and the fungicide are not identical.
  • the fungicide can be present either in the pesticidal terpene mixture component of the kit of parts or in the insecticide component of the kit of parts being spatially separated or in both of these components.
  • the fungicide is present in the insecticide component.
  • the kit of parts according to the present invention can additionally comprise at least one auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants as mentioned below.
  • This at least one auxiliary can be present either in the pesticidal terpene mixture component of the kit of parts or in the insecticide component of the kit of parts being spatially separated or in both of these components.
  • composition as described above is used for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, nematodes and/or phytopathogens.
  • composition as described above increases the overall plant health.
  • plant health generally comprises various sorts of improvements of plants that are not connected to the control of pests.
  • advantageous properties are improved crop characteristics including: emergence, crop yields, protein content, oil content, starch content, more developed root system, improved root growth, improved root size maintenance, improved root effectiveness, improved stress tolerance (e.g.
  • tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less input needed (such as fertilizers or water), less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, enhanced plant vigor, increased plant stand and early and better germination.
  • improved plant health preferably refers to improved plant characteristics including: crop yield, more developed root system (improved root growth), improved root size maintenance, improved root effectiveness, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, photosynthetic activity, more productive tillers, enhanced plant vigor, and increased plant stand.
  • improved plant health preferably especially refers to improved plant properties selected from crop yield, more developed root system, improved root growth, improved root size maintenance, improved root effectiveness, tillering increase, and increase in plant height.
  • the effect of a composition according to the present invention on plant health as defined herein can be determined by comparing plants which are grown under the same environmental conditions, whereby a part of said plants is treated with a composition according to the present invention and another part of said plants is not treated with a composition according to the present invention. Instead, said other part is not treated at all or treated with a placebo (i.e., an application without a composition according to the invention such as an application without all active ingredients (i.e. without a pesticidal terpene mixture as described herein and without an insecticide as described herein), or an application without a pesticidal terpene mixture as described herein, or an application without an insecticide as described herein.
  • a placebo i.e., an application without a composition according to the invention such as an application without all active ingredients (i
  • composition according to the present invention may be applied in any desired manner, such as in the form of a seed coating, soil drench, and/or directly in- furrow and/or as a foliar spray and applied either pre-emergence, post-emergence or both.
  • the composition can be applied to the seed, the plant or to harvested fruits and vegetables or to the soil wherein the plant is growing or wherein it is desired to grow (plant's locus of growth).
  • composition according to the present invention is used for treating conventional or transgenic plants or seed thereof.
  • Preferred plants and/or plant parts to be treated according to the invention are pepper ⁇ Capsicum annuum), cotton leaves (Gossypium hirsutum), bena plants (phaseolus vulgaris), Chinese cabbage (Brassica pekinensis), maize (Zeas perennial) and French beans (Phaesolus vulgaris).
  • composition of the invention has been proven to be particularly effective against infestation with green peach aphid (Myzus persicae), cotton aphid (Aphis gossypii), spotted spider mite (Tetranychus urticae), mustard beetle (Phaedon cochleriae), and fall armyworm (Spdoptera frugiperde).
  • green peach aphid Myzus persicae
  • cotton aphid Aphis gossypii
  • spotted spider mite Tetranychus urticae
  • mustard beetle Phaedon cochleriae
  • fall armyworm Spdoptera frugiperde
  • a method for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, nematodes and/or phytopathogens comprising the step of simultaneously or sequentially applying the pesticidal terpene mixture and at least one insecticide and optionally at least one fungicide on the plant, plant parts, harvested fruits, vegetables and/or plant's locus of growth in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide or fungicide are not identical.
  • the at least one insecticide is a synthetic insecticide.
  • the at least one fungicide is a synthetic fungicide.
  • the method of the present invention includes the following application methods, namely both of the pesticidal terpene mixture and the at least one insecticide mentioned before may be formulated into a single, stable composition with an agriculturally acceptable shelf life (so called “solo-formulation”), or being combined before or at the time of use (so called “combined-formulations").
  • the expression “combination” stands for the various combinations of the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide, in a solo-formulation, in a single "ready-mix” form, in a combined spray mixture composed from solo- formulations, such as a "tank-mix”, and especially in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other within a reasonably short period, such as a few hours or days, e.g. 2 hours to 7 days.
  • the order of applying the composition according to the present invention is not essential for working the present invention.
  • the term “combination” also encompasses the presence of the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide on or in a plant to be treated or its surrounding, habitat or storage space, e.g. after simultaneously or consecutively applying the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide to a plant its surrounding, habitat or storage space.
  • the pectidial terpene mixture and the at least one insecticide, and optionally the at least one fungicide are employed or used in a sequential manner, it is preferred to treat the plants or plant parts (which includes seeds and plants emerging from the seed), harvested fruits and vegetables according to the following method: Firstly applying the at least one insecticide and optionally the at least one fungicide on the plant or plant parts, and secondly applying the pesticidal terpene mixture Jo the same plant or plant parts.
  • the time periods between the first and the second application within a (crop) growing cycle may vary and depend on the effect to be achieved.
  • the first application is done to prevent an infestation of the plant or plant parts with insects, nematodes and/or phytopathogens (this is particularly the case when treating seeds) or to combat the infestation with insects, nematodes and/or phytopathogens (this is particularly the case when treating plants and plant parts) and the second application is done to prevent or control the infestation with insects, nematodes and/or phytopathogens.
  • Control in this context means that the pesticidal terpene mixture is not able to fully exterminate the pests or phytopathogenic fungi but is able to keep the infestation on an acceptable level.
  • the present invention also provides methods of enhancing the killing, inhibiting, preventative and/or repelling activity of the compositions of the present invention by multiple applications.
  • compositions of the present invention are applied to a plant and/or plant part for two times, during any desired development stages or under any predetermined pest pressure, at an interval of about 1 hour, about 5 hours, ab out 10 hours, about 24 hours, about two days, about 3 days, about 4 days, about 5 days, about 1 week, about 10 days, about two weeks, about three weeks, about 1 month or more.
  • compositions of the present invention are applied to a plant and/or plant part for more than two times, for example, 3 times, 4 times, 5 times, 6 times, 7 times, 8 times, 9 times, 10 times, or more, during any desired development stages or under any predetermined pest pressure, at an interval of about 1 hour, about 5 hours, about 10 hours, about 24 hours, about two days, about 3 days, about 4 days, about 5 days, about lweek, about 10 days, about two weeks, about three weeks, about 1 month or more.
  • the intervals between each application can vary if it is desired.
  • One skilled in the art will be able to determine the application times and length of interval depending on plant species, plant pest species, and other factors.
  • a very low level of residues of the at least one insecticide, and optionally at least one fungicide on the treated plant, plant parts, and the harvested fruits and vegetables can be achieved.
  • harvested fruits and vegetables with the composition according to the invention is carried out directly or by action on their surroundings, habitat or storage space using customary treatment methods, for example dipping, spraying, atomizing, irrigating, evaporating, dusting, fogging, broadcasting, foaming, painting, spreading-on, watering (drenching), drip irrigating.
  • customary treatment methods for example dipping, spraying, atomizing, irrigating, evaporating, dusting, fogging, broadcasting, foaming, painting, spreading-on, watering (drenching), drip irrigating.
  • plant to be treated encompasses every part of a plant including its root system and the material - e.g., soil or nutrition medium - which is in a radius of at least 10 cm, 20 cm, 30 cm around the caulis or bole of a plant to be treated or which is at least 10 cm, 20 cm, 30 cm around the root system of said plant to be treated, respectively.
  • the amount of the pesticidal terpene mixture which is used or employed in combination with the at least one insecticide, optionally in the presence of a fungicide depends on the final formulation as well as size or type of the plant, plant parts, seeds, harvested fruits and vegetables to be treated.
  • the pesticidal terpene mixture to be employed or used according to the invention is present in about 2 % to about 80 % (w/w), preferably in about 5 % to about 75 % (w/w), more preferably about 10 % to about 70 % (w/w) of its solo-formulation or combined- formulation with the at least one insecticide, and optionally the fungicide.
  • the amount of the at least one insecticide which is used or employed in combination with the pesticidal terpene mixture, optionally in the presence of a fungicide depends on the final formulation as well as size or type of the plant, plant parts, seeds, harvested fruit or vegetable to be treated.
  • the insecticide to be employed or used according to the invention is present in about 0.1 % to about 80 % (w/w), preferably 1 % to about 60 % (w/w), more preferably about 10 % to about 50 % (w/w) of its 5 solo-formulation or combined- formulation with the pesticidal terpene mixture, and optionally the fungicide.
  • the pesticidal terpene mixture and at least one insecticide, and if present also the fungicide are used or employed in a synergistic weight ratio.
  • the skilled person is able to find out the synergistic weight ratios for the present invention by routine methods.
  • the skilled person understands that these ratios refer to the ratio within a combined-formulation as well as to the calculative ratio of the pesticidal terpene mixture described herein and the at least one insecticide when both components are applied as mono- formulations to a plant to be treated.
  • the skilled person can calculate this ratio by simple mathematics since the volume and the amount of the pesticidal terpene mixture and insecticide, respectively, in a mono-formulation is known to the skilled person.
  • the ratio can be calculated based on the amount of the at least one insecticide, at the time point of applying said component of a combination according to the invention to a plant or plant part and the amount of the pesticidal terpene mixture shortly prior (e.g., 48 h, 24 h, 12 h, 6 h, 2 h, 1 h) or at the time point of applying said component of a combination according to the invention to a plant or plant part.
  • the application of the pesticidal terpene mixture and the at least one insecticide to a plant or a plant part can take place simultaneously or at different times as long as both components are present on or in the plant after the application(s).
  • the skilled person can determine the concentration of the insecticide on/in a plant by chemical analysis known in the art, at the time point or shortly before the time point of applying the pesticidal terpene mixture.
  • the concentration of the pesticidal terpene mixture can be determined using test which are also known in the art, at the time point or shortly before the time point of applying the insecticide.
  • the synergistic weight ratio of the pesticidal terpene mixture and the at least one insecticide lies in the range of 1 : 1000 to 1000 : 1, preferably in the range of 1 : 500 to 500 : 1, more preferably in the range of 1 : 500 to 300 : 1.
  • a ratio of 100: 1 means 100 weight parts of pesticidal terpene mixture and 1 weight part of the insecticide are combined (either as a solo formulation, a combined formulation or by separate applications to plants so that the combination is formed on the plant).
  • composition to be employed or used according to the present invention may vary.
  • the skilled person is able to find the appropriate application rate by way of routine experiments.
  • the present invention therefore also relates in particular to a method for protecting seed and germinating plants from attack by pests, by treating the seed with the pesticidal terpene mixture as defined above and at least one insecticide and optionally at least one fungicide of the invention.
  • the method of the invention for protecting seed and germinating plants from attack by pests encompasses a method in which the seed is treated simultaneously in one operation with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide. It also encompasses a method in which the seed is treated at different times with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide.
  • the invention relates to the use of the composition of the invention for treating seed for the purpose of protecting the seed and the resultant plant against insects, mites, nematodes and/or phytopathogens.
  • the invention also relates to seed which at the same time has been treated with the pesticidal terpene mixture and at least one insecticide, and optionally at least one fungicide.
  • the invention further relates to seed which has been treated at different times with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide.
  • the individual active ingredients in the composition of the invention may be present in different layers on the seed.
  • the invention relates to seed which, following treatment with the composition of the invention, is subjected to a film-coating process in order to prevent dust abrasion of the seed.
  • One of the advantages of the present invention is that, owing to the particular systemic properties of the compositions of the invention, the treatment of the seed with these compositions provides protection from insects, nematodes and/or phytopathogens not only to the seed itself but also to the plants originating from the seed, after they have emerged. In this way, it may not be necessary to treat the crop directly at the time of sowing or shortly thereafter. ?
  • a further advantage is to be seen in the fact that, through the treatment of the seed with composition of the invention, germination and emergence of the treated seed may be promoted.
  • composition of the invention may also be used, in particular, on transgenic seed. It is also stated that the composition of the invention may be used in combination with agents of the signalling technology, as a result of which, for example, colonization with symbionts is improved, such as rhizobia, mycorrhiza and/or endophytic bacteria, for example, is enhanced, and/or nitrogen fixation is optimized.
  • agents of the signalling technology such as rhizobia, mycorrhiza and/or endophytic bacteria, for example, is enhanced, and/or nitrogen fixation is optimized.
  • compositions of the invention are suitable for protecting seed of any variety of plant which is used in agriculture, in greenhouses, in forestry or in horticulture. More particularly, the seed in question is that of cereals (e.g. wheat, barley, rye, oats and millet), maize, cotton, soybeans, rice, potatoes, sunflower, coffee, tobacco, canola, oilseed rape, beets (e.g. sugar beet and fodder beet), peanuts, vegetables (e.g. tomato, cucumber, bean, brassicas, onions and lettuce), fruit plants, lawns and ornamentals. Particularly important is the treatment of the seed of cereals (such as wheat, barley, rye and oats) maize, soybeans, cotton, canola, oilseed rape and rice.
  • cereals e.g. wheat, barley, rye, oats and millet
  • maize cotton
  • soybeans rice
  • potatoes sunflower
  • coffee tobacco
  • canola oilseed rape
  • the seed in question here is that of plants which generally contain at least one heterologous gene that controls the expression of a polypeptide having, in particular, insecticidal and/or nematicidal properties.
  • These heterologous genes in transgenic seed may come from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium.
  • the present invention is particularly suitable for the treatment of transgenic seed which contains at least one heterologous gene from Bacillus sp.
  • the heterologous gene in question comes from Bacillus thuringiensis.
  • the composition of the invention is applied alone or in a suitable formulation to the seed.
  • the seed is preferably treated in a condition in which its stability is such that no damage occurs in the course of the treatment.
  • the seed may be treated at any point in time between harvesting and sowing.
  • seed is used which has been separated from the plant and has had cobs, hulls, stems, husks, hair or pulp removed.
  • seed may be used that has been harvested, cleaned and dried to a moisture content of less than 15% by weight.
  • seed can also be used that after drying has been treated with water, for example, and then dried again.
  • compositions of the invention can be applied directly, in other words without comprising further components and without having been diluted.
  • suitable formulations and methods for seed treatment are known to the skilled person and are described in, for example, the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 Al, WO 2002/080675 Al, WO 2002/028186 A2.
  • the combinations which can be used in accordance with the invention may be converted into the customary seed-dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other coating compositions for seed, and also ULV formulations.
  • customary seed-dressing formulations such as solutions, emulsions, suspensions, powders, foams, slurries or other coating compositions for seed, and also ULV formulations.
  • compositions are prepared in a known manner, by mixing composition with customary adjuvants, such as, for example, customary extenders and also solvents or diluents, colorants, wetters, dispersants, emulsifiers, antifoams, preservatives, secondary thickeners, stickers, gibberellins, and also water.
  • Colorants which may be present in the seed-dressing formulations which can be used in accordance with the invention include all colorants which are customary for such purposes. In this context it is possible to use not only pigments, which are of low solubility in water, but also water-soluble dyes. Examples include the colorants known under the designations Rhodamin B, C.I. Pigment Red 112 and C.I. Solvent Red 1.
  • Wetters which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the substances which promote wetting and which are customary in the formulation of active agrochemical ingredients. Use may be made preferably of alkylnaphthalenesulphonates, such as diisopropyl- or diisobutyl-naphthalenesulphonates.
  • Dispersants and/or emulsifiers which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the nonionic, anionic and cationic dispersants that are customary in the formulation of active agrochemical ingredients. Use may be made preferably of nonionic or anionic dispersants or of mixtures of nonionic or anionic dispersants. Suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide block polymers, alkylphenol polyglycol ethers and also tristryrylphenol polyglycol ethers, and the phosphated or sulphated derivatives of these.
  • Suitable anionic dispersants are, in particular, lignosulphonates, salts of polyacrylic acid, and arylsulphonate-formaldehyde condensates.
  • Antifoams which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the foam inhibitors that are customary in the formulation of active agrochemical ingredients. Use may be made preferably of silicone antifoams and magnesium stearate.
  • Preservatives which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the substances which can be employed for such purposes in agrochemical compositions. Examples include dichlorophen and benzyl alcohol hemiformal.
  • Secondary thickeners which may be present in the seed-dressing formulations which can be used in accordance with the invention include all substances which can be used for such purposes in agrochemical compositions. Those contemplated with preference include cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and highly disperse silica.
  • Stickers which may be present in the seed-dressing formulations which can be used in accordance with the invention include all customary binders which can be used in seed-dressing products. Preferred mention may be made of polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose.
  • the gibberellins are known (cf. R. Wegler, "Chemie der convinced- und Schadlingsbekampfungsstoff", Volume 2, Springer Verlag, 1970, pp. 401-412).
  • the seed-dressing formulations which can be used in accordance with the invention may be used, either directly or after prior dilution with water, to treat seed of any of a wide variety of types. Accordingly, the concentrates or the preparations obtainable from them by dilution with water may be employed to dress the seed of cereals, such as wheat, barley, rye, oats and triticale, and also the seed of maize, rice, oilseed rape, peas, beans, cotton, sunflowers and beets, or else the seed of any of a very wide variety of vegetables.
  • the seed-dressing formulations which can be used in accordance with the invention, or their diluted preparations may also be used to dress seed of transgenic plants. In that case, additional synergistic effects may occur in interaction with the substances formed through expression.
  • suitable mixing equipment includes all such equipment which can typically be employed for seed dressing. More particularly, the procedure when carrying out seed dressing is to place the seed in a mixer, to add the particular desired amount of seed-dressing formulations, either as such or following dilution with water beforehand, and to carry out mixing until the distribution of the formulation on the seed is uniform. This may be followed by a drying operation.
  • the application rate of the seed-dressing formulations which can be used in accordance with the invention may be varied within a relatively wide range.
  • the application rates in the case of the composition are situated generally at between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
  • composition according to the invention in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in protection of stored products and of materials, and in the hygiene sector. They can be preferably employed as plant protection agents.
  • the present invention relates to the use of the composition according to the invention as insecticide and/or fungicide.
  • composition according to the invention in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in protection of stored products and of materials, and in the hygiene sector. They can be preferably employed as plant protection agents.
  • the present invention relates to the use of the composition according to the invention as insecticide and/or fungicide.
  • the present composition preferably is active against normally sensitive and resistant species and against all or some stages of development.
  • the abovementioned pests include: pests from the phylum Arthropoda, especially from the class Arachnida, for example, Acarus spp., Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eri
  • the order Blattodea for example, Blattella asahinai, Blattella germanica, Blatta orientalis, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta spp., Supella longipalpa; from the order Coleoptera, for example, Acalymma vittatum, Acanthoscelides obtectus, Adoretus spp., Agelastica alni, Agriotes spp., Alphitobius diaperinus, Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Anthonomus spp., Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., Attagenus spp., Bruchidius obtectus, Bruchus spp., Cassida spp., Cero
  • the composition according to the present invention has potent microbicidal activity and can be used for control of unwanted microorganisms, such as fungi and bacteria, in crop protection and in the protection of materials.
  • the invention also relates to a method for controlling unwanted microorganisms, characterized in that the inventive composition is applied to the phytopathogenic fungi, phytopathogenic bacteria and/or their habitat.
  • Fungicides can be used in crop protection for control of phytopathogenic fungi. They are characterized by an outstanding efficacy against a broad spectrum of phytopathogenic fungi, including soilborne pathogens, which are in particular members of the classes Plasmodiophoromycetes , Peronosporomycetes (Syn. Oomycetes), Chytridiomycetes , Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes (Syn. Fungi imperfecti). Some fungicides are systemically active and can be used in plant protection as foliar, seed dressing or soil fungicide. Furthermore, they are suitable for combating fungi, which inter alia infest wood or roots of plant.
  • Bactericides can be used in crop protection for control of Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
  • Non-limiting examples of pathogens of fungal diseases which can be treated in accordance with the invention include: diseases caused by powdery mildew pathogens, for example Blumeria species, for example Blumeria graminis; Podosphaera species, for example Podosphaera leucotricha; Sphaerotheca species, for example Sphaerotheca fuliginea; Uncinula species, for example Uncinula necator; diseases caused by rust disease pathogens, for example Gymnosporangium species, for example Gymnosporangium sabinae; Hemileia species, for example Hemileia vastatrix; Phakopsora species, for example Phakopsora pachyrhizi and Phakopsora meibomiae; Puccinia species, for example Puccinia recondite, P.
  • diseases caused by powdery mildew pathogens for example Blumeria species, for example Blumeria graminis
  • Urocystis species for example Urocystis occulta
  • Ustilago species for example Ustilago nuda, U. nuda tritici
  • Botrytis species for example Botrytis cinerea
  • Penicillium species for example Penicillium expansum and P.
  • Sclerotinia species for example Sclerotinia sderotiorum
  • Verticilium species for example Verticilium alboatrum
  • seed and soilborne decay, mould, wilt, rot and damping-off diseases caused, for example, by Alternaria species, caused for example by Alternaria brassicicola
  • Aphanomyces species caused for example by Aphanomyces euteiches
  • Ascochyta species caused for example by Ascochyta lentis
  • Aspergillus species caused for example by Aspergillus flavus
  • Cladosporium species caused for example by Cladosporium herbarum
  • Cochliobolus species caused for example by Cochliobolus sativus
  • Colletotrichum species caused for example by Colletotrichum coccodes
  • Fusarium species caused for example by Fusarium cul
  • Taphrina species for example Taphrina deformans
  • decline diseases of wooden plants caused, for example, by Esca disease caused for example by Phaemoniella clamydospora, Phaeoacremonium aleophilum and Fomitiporia mediterranea
  • Eutypa dyeback caused for example by Eutypa lata
  • Ganoderma diseases caused for example by Ganoderma boninense
  • Rigidoporus diseases caused for example by Rigidoporus lignosus
  • diseases of flowers and seeds caused, for example, by Botrytis species, for example Botrytis cinerea
  • Botrytis species for example Botrytis cinerea
  • - - diseases of plant tubers caused, for example, by Rhizoctonia species, for example Rhizoctonia solani
  • Helminthosporium species for example Helminthosporium solani
  • Helminthosporium species for example Helminthosporium solani
  • Plasmodiophora species for example Plamodiophora brassicae
  • diseases caused by bacterial pathogens for example Xanthomonas species, for example Xanthomonas campestris pv. oryzae
  • Pseudomonas species for example Pseudomonas syringae pv. lachrymans
  • Erwinia species for example Erwinia amylovora.
  • phytophthora rot (Phytophthora megasperma), brown stem rot (Phialophora gregata), pythium rot (Pythium aphanidermatum, Pythium irregulare, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), rhizoctonia root rot, stem decay, and damping-off (Rhizoctonia solani), sclerotinia stem decay (Sclerotinia sclerotiorum), sclerotinia southern blight (Sclerotinia rolfsii), thielaviopsis root rot (Thielaviopsis basicola).
  • inventive compositions can be used for curative or protective/preventive control of phytopathogenic fungi.
  • the invention therefore also relates to curative and protective methods for controlling phytopathogenic fungi by the use of the inventive composition, which is applied to the seed, the plant or plant parts, the fruit or the soil in which the plants grow.
  • the fact that the composition is well tolerated by plants at the concentrations required for controlling plant diseases allows the treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil.
  • plants and plant parts can be treated.
  • plants are meant all plants and plant populations such as desirable and undesirable wild plants, cultivars and plant varieties (whether or not protectable by plant variety or plant breeder's rights).
  • Cultivars and plant varieties can be plants obtained by conventional propagation and breeding methods which can be assisted or supplemented by one or more biotechnological methods such as by use of double haploids, protoplast fusion, random and directed mutagenesis, molecular or genetic markers or by bioengineering and genetic engineering methods.
  • plant parts are meant all above ground and below ground parts and organs of plants such as shoot, leaf, blossom and root, whereby for example leaves, needles, stems, branches, blossoms, fruiting bodies, fruits and seed as well as roots, corms and rhizomes are listed.
  • Crops and vegetative and generative propagating material for example cuttings, corms, rhizomes, runners and seeds also belong to plant parts.
  • the inventive composition when it is well tolerated by plants, has favourable homeotherm toxicity and is well tolerated by the environment, is suitable for protecting plants and plant organs, for enhancing harvest yields, for improving the quality of the harvested material. It can preferably be used as crop protection composition. It is active against normally sensitive and resistant species and against all or some stages of development.
  • Plants which can be treated in accordance with the invention include the following main crop plants: maize, soya bean, alfalfa, cotton, sunflower, Brassica oil seeds such as Brassica napus (e.g. canola, rapeseed), Brassica rapa, B. juncea (e.g. (field) mustard) and Brassica carinata, Arecaceae sp. (e.g. oilpalm, coconut), rice, wheat, sugar beet, sugar cane, oats, rye, barley, millet and sorghum, triticale, flax, nuts, grapes and vine and various fruit and vegetables from various botanic taxa, e.g. Rosaceae sp. (e.g.
  • pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds, plums and peaches, and berry fruits such as strawberries, raspberries, red and black currant and gooseberry), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp. (e.g. olive tree), Actinidaceae sp., Lauraceae sp. (e.g. avocado, cinnamon, camphor), Musaceae sp. (e.g.
  • Rubiaceae sp. e.g. coffee
  • Theaceae sp. e.g. tea
  • Sterculiceae sp. e.g. lemons, oranges, mandarins and grapefruit
  • Solanaceae sp. e.g. tomatoes, potatoes, peppers, capsicum, aubergines, tobacco
  • Liliaceae sp. Compositae sp. (e.g. lettuce, artichokes and chicory - including root chicory, endive or common chicory), Umbelliferae sp. (e.g.
  • Cucurbitaceae sp. e.g. cucumbers - including gherkins, pumpkins, watermelons, calabashes and melons
  • AUiaceae sp. e.g. leeks and onions
  • Cruciferae sp. e.g. white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes, horseradish, cress and Chinese cabbage
  • Leguminosae sp. e.g. peanuts, peas, lentils and beans - e.g. 5 common beans and broad beans
  • Chenopodiaceae sp. e.g.
  • the treatment according to the invention may also result in super-additive (“synergistic”) effects.
  • compositions in the treatment according to the invention may also have a strengthening effect in plants.
  • the defense system of the plant against attack by unwanted phytopathogenic fungi and/ or microorganisms and/or viruses is mobilized.
  • Plant-strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted phytopathogenic fungi and/or microorganisms and/or viruses, the treated plants display a substantial degree of resistance to these phytopathogenic fungi and/or microorganisms and/or viruses,
  • composition according to the present invention in the treatment according to the invention plants can be protected against attack by the abovementioned pathogens within a certain period of time after the treatment.
  • the period of time within which protection is effected generally extends from 1 to 10 days, preferably 1 to 7 days, after the treatment of the plants with the active ingredients
  • Plants and plant cultivars which are also preferably to be treated according to the invention are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.
  • Plants and plant cultivars which may also be treated according to the invention are those plants which are resistant to one or more abiotic stresses, i. e. that already exhibit an increased plant health with respect to stress tolerance.
  • Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozon exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of 5 phosphorus nutrients, shade avoidance.
  • the treatment of these plants and cultivars with the composition of the present invention additionally increases the overall plant health (cf. above).
  • Plants and plant cultivars which may also be treated according to the invention are those plants characterized by enhanced yield characteristics i. e. that already exhibit an increased plant health with respect to this feature. Increased yield in said plants can be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency and accelerated maturation.
  • Yield can furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance.
  • Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability.
  • the treatment of these plants and cultivars with the composition of the present invention additionally increases the overall plant health (cf. above).
  • Plants that may be treated according to the invention are hybrid plants that already express the characteristic of heterosis or hybrid vigor which results in generally higher yield, vigor, health and resistance towards biotic and abiotic stress factors. Such plants are typically made by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent). Hybrid seed is typically harvested from the male sterile plants and sold to growers. Male sterile plants can sometimes (e.g. in corn) be produced by detasseling, i.e. the mechanical removal of the male reproductive organs (or males flowers) but, more typically, male sterility is the result of genetic determinants in the plant genome.
  • male sterile plants can also be obtained by plant biotechnology methods such as genetic engineering.
  • a particularly useful means of obtaining male-sterile plants is described in WO 89/10396 in which, for example, a ribonuclease such as barnase is selectively expressed in the tapetum cells in the stamens. Fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar.
  • Plants or plant cultivars which may be treated according to the invention are herbicide-tolerant plants, i.e. plants made tolerant to one or 5 more given herbicides. Such plants can be obtained either by genetic transformation, or by selection of plants containing a mutation imparting such herbicide tolerance.
  • Herbicide-tolerant plants are for example glyphosate-tolerant plants, i.e. plants made tolerant to the herbicide glyphosate or salts thereof. Plants can be made tolerant to glyphosate through different means.
  • glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS).
  • EPSPS 5-enolpyruvylshikimate-3-phosphate synthase
  • EPSPS 5-enolpyruvylshikimate-3-phosphate synthase
  • Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate oxido-reductase enzyme. Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate acetyl transferase enzyme. Glyphosate-tolerant plants can also be obtained by selecting plants containing naturally- occurring mutations of the above-mentioned genes.
  • herbicide resistant plants are for example plants that are made tolerant to herbicides inhibiting the enzyme glutamine synthase, such as bialaphos, phosphinothricin or glufosinate.
  • Such plants can be obtained by expressing an enzyme detoxifying the herbicide or a mutant glutamine synthase enzyme that is resistant to inhibition.
  • One such efficient detoxifying enzyme is an enzyme encoding a phosphinothricin acetyltransferase (such as the bar or pat protein from Streptomyces species). Plants expressing an exogenous phosphinothricin acetyltransferase are also described.
  • hydroxyphenylpyruvatedioxygenase HPPD
  • Hydroxyphenylpyruvatedioxygenases are enzymes that catalyze the reaction in which para-hydroxyphenylpyruvate (HPP) is transformed into homogentisate.
  • Plants tolerant to HPPD-inhibitors can be transformed with a gene encoding a naturally- occurring resistant HPPD enzyme, or a gene encoding a mutated HPPD enzyme.
  • Tolerance to HPPD- inhibitors can also be obtained by transforming plants with genes encoding certain enzymes enabling the formation of homogentisate despite the inhibition of the native HPPD enzyme by the HPPD-inhibitor.
  • Tolerance of plants to HPPD inhibitors can also be improved by transforming plants with a gene encoding an enzyme prephenate dehydrogenase in addition to a gene encoding an HPPD-tolerant enzyme.
  • Still further herbicide resistant plants are plants that are made tolerant to aceto lactate synthase (ALS) inhibitors.
  • ALS-inhibitors include, for example, sulfonylurea, imidazolinone, triazolopyrimidines, pyrimidinyoxy(thio)benzoates, and/or sulfonylaminocarbonyltriazolinone herbicides.
  • Different mutations in the ALS enzyme also known as acetohydroxyacid synthase, AHAS
  • AHAS acetohydroxyacid synthase
  • the production of sulfonylurea-tolerant plants and imidazolinone-tolerant plants is described in WO 1996/033270. Other 5 imidazolinone-tolerant plants are also described. Further sulfonylurea- and imidazolinone-tolerant plants are also described in for example WO 2007/024782.
  • plants tolerant to imidazolinone and/or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide or mutation breeding as described for example for soybeans, for rice, for sugar beet, for lettuce, or for sunflower.
  • Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering which may also be treated according to the invention are insect-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.
  • An "insect-resistant transgenic plant”, as used herein, includes any plant containing at least one transgene comprising a coding sequence encoding:
  • insecticidal crystal protein from Bacillus thuringiensis or an insecticidal portion thereof, such as the insecticidal crystal proteins listed online at:
  • insecticidal portions thereof e.g., proteins of the Cry protein classes CrylAb, CrylAc, CrylF, Cry2Ab, Cry3Aa, or Cry3Bb or insecticidal portions thereof; or
  • a crystal protein from Bacillus thuringiensis or a portion thereof which is insecticidal in the presence of a second other crystal protein from Bacillus thuringiensis or a portion thereof, such as the binary toxin made up of the Cry34 and Cry35 crystal proteins; or
  • a hybrid insecticidal protein comprising parts of different insecticidal crystal proteins from Bacillus thuringiensis, such as a hybrid of the proteins of 1) above or a hybrid of the proteins of 2) above, e.g., the CrylA.105 protein produced by corn event MON98034 (WO 2007/027777); or
  • VIP vegetative insecticidal
  • secreted protein from Bacillus thuringiensis or Bacillus cereus which is insecticidal in the presence of a second secreted protein from Bacillus thuringiensis or B. cereus, such as the binary toxin made up of the VIP1 A and VIP2A proteins; or 5
  • hybrid insecticidal protein comprising parts from different secreted proteins from Bacillus thuringiensis or Bacillus cereus, such as a hybrid of the proteins in 1) above or a hybrid of the proteins in 2) above; or
  • an insect-resistant transgenic plant also includes any plant comprising a combination of genes encoding the proteins of any one of the above classes 1 to 8.
  • an insect-resistant plant contains more than one transgene encoding a protein of any one of the above classes 1 to 8, to expand the range of target insect species affected when using different proteins directed at different target insect species, or to delay insect resistance development to the plants by using different proteins insecticidal to the same target insect species but having a different mode of action, such as binding to different receptor binding sites in the insect.
  • Plants or plant cultivars which may also be treated according to the invention are nematode resistant plants.
  • Examples of nematode resistant plants are described in e.g. US Patent Application Nos 11/765,491, 11/765,494, 10/926,819, 10/782,020, 12/032,479, 10/783,417, 10/782,096, 11/657,964, 12/192,904, 11/396,808, 12/166,253, 12/166,239, 12/166,124, 12/166,209, 11/762,886, 12/364,335, 11/763,947, 12/252,453, 12/209,354, 12/491,396 or 12/497,221.
  • Plants or plant cultivars obtained by plant biotechnology methods such as genetic engineering which may also be treated according to the invention are tolerant to abiotic stresses. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such stress resistance. Particularly useful stress tolerance plants include:
  • plants which contain a stress tolerance enhancing transgene capable of reducing the expression and/or the activity of the poly(ADP-ribose)glycohydrolase (PARG) encoding genes of the plants or plants cells.
  • PARG poly(ADP-ribose)glycohydrolase
  • plants which contain a stress tolerance enhancing transgene coding for a plant-functional enzyme of the nicotinamide adenine dinucleotide salvage synthesis pathway including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid mononucleotide adenyl transferase, nicotinamide adenine dinucleotide synthetase or nicotine amide phosphorybosyltransferase.
  • Plants or plant cultivars which may also be treated according to the invention show altered quantity, quality and/or storage-stability of the harvested product and/or altered properties of specific ingredients of the harvested product such as :
  • transgenic plants which synthesize a modified starch, which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications.
  • a modified starch which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications.
  • transgenic plants which synthesize non starch carbohydrate polymers or which synthesize non starch carbohydrate polymers with altered properties in comparison to wild type plants without genetic modification.
  • Examples are plants producing polyfructose, especially of the inulin and levan-type, plants producing alpha 1,4 glucans, plants producing alpha- 1,6 branched alpha- 1,4- glucans, plants producing alternan,
  • Plants or plant cultivars which may also be treated according to the invention are plants, such as cotton plants, with altered fiber characteristics.
  • plants can be obtained by genetic transformation or by selection of plants contain a mutation imparting such altered fiber characteristics and include:
  • Plants such as cotton plants, containing an altered form of cellulose synthase genes
  • Plants such as cotton plants, containing an altered form of rsw2 or rsw3 homologous nucleic acids
  • Plants such as cotton plants, having fibers with altered reactivity, e.g. through the expression of N-acteylglucosaminetransferase gene including nodC and chitinsynthase genes.
  • Plants or plant cultivars which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered oil profile characteristics. Such plants can be obtained by genetic transformation or by selection of plants contain a mutation imparting such altered oil characteristics and include:
  • transgenic plants which may be treated according to the invention are plants which comprise one or more genes which encode one or more toxins, such as the following which are sold under the trade names YIELD GARD ® (for example maize, cotton, soya beans), KnockOut ® (for example maize), BiteGard ® (for example maize), Bt-Xtra ® (for example maize), StarLink ® (for example maize), Bollgard ® (cotton), Nucotn ® (cotton), Nucotn 33B ® (cotton), NatureGard ® (for example maize), Protecta® and NewLeaf ® (potato).
  • YIELD GARD ® for example maize, cotton, soya beans
  • KnockOut ® for example maize
  • BiteGard ® for example maize
  • Bt-Xtra ® for example maize
  • StarLink ® for example maize
  • Bollgard ® cotton
  • Nucotn ® cotton
  • Nucotn 33B ®
  • herbicide-tolerant plants examples include maize varieties, cotton varieties and soya bean varieties which are sold under the trade names Roundup Ready ® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link ® (tolerance to phosphinotricin, for example oilseed rape), IMI ® (tolerance to imidazolinones) and STS ® (tolerance to sulphonylureas, for example maize).
  • Herbicide-resistant plants plants bred in a conventional manner for herbicide tolerance
  • Clearfield ® for example maize.
  • Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or a combination of transformation events, and that are listed for example in the databases for various national or regional regulatory agencies including Event 1143-14A (cotton, insect control, not deposited, described in WO 06/128569); Event 1143-51B (cotton, insect control, not deposited, described in WO 06/128570); Event 1445 (cotton, herbicide tolerance, not deposited, described in US-A 2002-120964 or WO 02/034946); Event 17053 (rice, herbicide tolerance, deposited as PTA-9843, described in WO 10/117737); Event 17314 (rice, herbicide tolerance, deposited as PTA-9844, described in WO 10/117735); Event 281-24-236 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in WO 05/103266 or US-A 2005-216969); Event 3006- 210-23 (cotton, insect control - herbicide tolerance, deposited
  • Event CE43-67B (cotton, insect control, deposited as DSM ACC2724, described in US-A 2009-217423 or WO 06/128573); Event CE44-69D (cotton, insect control, not deposited, described in US-A 2010-0024077); Event CE44-69D (cotton, insect control, not deposited, described in WO 06/128571); Event CE46-02A (cotton, insect control, not deposited, described in WO 06/128572); Event COT102 (cotton, insect control, not deposited, described in US-A 2006-130175 or WO 04/039986); Event COT202 (cotton, insect control, not deposited, described in US-A 2007-067868 or WO 05/054479); Event COT203 (cotton, insect control, not deposited, described in WO 05/054480); Event 5?
  • DAS40278 (corn, herbicide tolerance, deposited as ATCC PTA-10244, described in WO 11/022469); Event DAS-59122-7 (corn, insect control - herbicide tolerance, deposited as ATCC PTA 11384 , described in US-A 2006-070139); Event DAS-59132 (corn, insect control - herbicide tolerance, not deposited, described in WO 09/100188); Event DAS68416 (soybean, herbicide tolerance, deposited as ATCC PTA-10442, described in WO 11/066384 or WO 11/066360); Event DP-098140-6 (corn, herbicide tolerance, deposited as ATCC PTA-8296, described in US-A 2009-137395 or WO 08/112019); Event DP-305423-1 (soybean, quality trait, not deposited, described in US-A 2008-312082 or WO 08/054747); Event DP-32138-1 (corn, hybridization system, deposited as ATCC PTA-9158,
  • MON87705 (soybean, quality trait - herbicide tolerance, deposited as ATCC PTA-9241, described in US-A 2010-0080887 or WO 10/037016); Event MON87708 (soybean, herbicide tolerance, deposited as ATCC PTA9670, described in WO 11/034704); Event MON87754 (soybean, quality trait, deposited as ATCC PTA-9385, described in WO 10/024976); Event MON87769 (soybean, quality trait, deposited as ATCC PTA-8911, described in US-A 2011-0067141 or WO 09/102873); Event MON88017 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-5582, described in US-A 2008-028482 or WO 05/059103); Event MON88913 (cotton, herbicide tolerance, deposited as ATCC PTA-4854, described in WO 04/072235 or US-A 2006-
  • transgenic plants which may be treated according to the invention are plants containing transformation events, or combination of transformation events, that are listed for example in the databases from various national or regional regulatory agencies (see for example http://gmoinfo.jrc.it/gmp_browse.aspx and http://www.agbios.com/dbase.php).
  • Emulsifier 2 parts by weight of alkylaryl polyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration, if necessary.
  • Pepper leaves ⁇ Capsicum annuum) which are heavily infested by the green peach aphid ⁇ Myzus persicae) are treated by being sprayed with the preparation of the active compound of the desired concentration.
  • mortality in % is determined. 100 % means all the aphids have been killed; 0 % means none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
  • Emulsifier 2 parts by weight of alkylaryl polyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration, if necessary.
  • Cotton leaves which are heavily infested by the cotton aphid ⁇ Aphis gossypii) are treated by being sprayed with the preparation of the active compound of the desired concentration. After the specified period of time, the mortality in % is determined. 100 % means all the aphids have been killed; 0 % means none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
  • Emulsifier 2 parts by weight of alkylaryl polyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration if necessary.
  • Bean plants Phaseolus vulgaris which are heavily infested with all stages of the two-spotted spider mite (Tetranychus urticae) are treated by being sprayed with the preparation of the active compound of the desired concentration. After the specified period of time, mortality in % is determined. 100 % means all the spider mites have been killed; 0 % means none of the spider mites have been killed. The mortality values determined thus are recalculated using the Colby-formula (see above).
  • Emulsifier 0.5 parts by weight of alkylaryl polyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Emulsifier 0.5 parts by weight alkylarylpolyglycolether
  • a suitable preparation of the active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Maize ⁇ Zea perennial flowergrass Plant ⁇ Zea perennial flowergrass. Once dry, the leaf sections are infested with fall armyworm larvae ⁇ Spodoptera frugiperda).
  • mortality in % is determined. 100% means all caterpillars have been killed and 0% means none of the caterpillars have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
  • SPODFR Spodoptera frugiperda -test
  • Emulsifier 1 part by weight of alkylaryl polyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration if necessary.
  • Maize leaves ⁇ Zea grass are treated by being sprayed with the preparation of the active compound of the desired concentration and are infested with caterpillars of the fall army worm ⁇ Spodoptera frugiperda).
  • the mortality values determined thus are recalculated using the Colby-formula (see above). After the specified period of time, mortality in % is determined. 100 % means all the caterpillars have been killed; 0 % means none of the caterpillars have been killed.
  • Emulsifier 0.5 parts by weight alkylarylpolyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • Emulsifier 0.5 parts by weight alkylarylpolyglycolether
  • a suitable preparation of active compound 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration.
  • the spores are diluted with emulsifier- containing water to the desired concentration.
  • French beans Phaseolus vulgaris which are heavily infested with all stages of the two spotted spidermite (Tetranychus urticae), are sprayed with a preparation of the active ingredient of the desired concentration.

Abstract

The present invention relates to a composition comprising a) a pesticidal terpene mixture comprising, as pesticidally active chemical compounds, α-terpinene, p-cymene and limonene and b) at least one insecticide selected from the group consisting of Abamectin, Acephate, Acetamiprid, Acrinathrin, Afidopyropen, Alpha-Cypermethrin, Azadirachtin, Bacillus firmus, Beta-Cyfluthrin, Bifenthrin, Buprofezin, Clothianidin, Chlorantraniliprole, Chlorfenapyr, Chlorpyrifos, Carbofuran, Cyantraniliprole, Cyenopyrafen, Cyflumentofen, Cyfluthrin, Cypermethrin, Deltamethrin, Diafenthiuron, Dinotefuran, Emamectin-benzoate, Ethiprole, Fenpyroximate, Fipronil, Flometoquin, Flonicamid, Flubendiamide, Fluensulfone, Fluopyram, Flupyradifurone, Gamma- Cyhalothrin, Imidacloprid, Indoxacarb, Lambda- Cyhalothrin, Lufenuron, Metaflumizone, Methiocarb, Methoxyfenozide, Milbemectin, Profenofos, Pyflubumide, Pymetrozine, Pyrifluquinazone, Spinetoram, Spinosad, Spirodiclofen, Spiromesifen, Spirotetramate, Sulfoxaflor, Tebufenpyrad, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, Triflumuron, 1-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)-1H-tetrazol-1-yl]methyl} -1H-pyrazole-5-carboxamide, 1-(3-chloropyridin-2-yl)-N- [4- cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl}-1H- pyrazole-5-carboxamide and 1- {2-fluoro-4-methyl-5-[(2,2,2-trifluorethyl)sulfinyl]phenyl} -3- (trifluoromethyl)-1H-1,2,4-triazol-5-amine in a synergistically effective amount, and optionally a fungicide. Furthermore, the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.

Description

Compositions comprising a pesticidal terpene mixture and an insecticide
The present invention relates to a composition comprising a pesticidal terpene mixture and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical. Furthermore, the present invention relates to the use of this composition as well as a method for reducing overall damage of plants and plant parts.
Synthetic insecticides or fungicides often are non-specific and therefore can act on organisms other than the target ones, including other naturally occurring beneficial organisms. Because of their chemical nature, they may be also toxic and non-biodegradable. Consumers worldwide are increasingly conscious of the potential environmental and health problems associated with the residuals of chemicals, particularly in food products. This has resulted in growing consumer pressure to reduce the use or at least the quantity of chemical (i. e. synthetic) pesticides. Thus, there is a need to manage food chain requirements while still allowing effective pest control.
A further problem arising with the use of synthetic insecticides or fungicides is that the repeated and exclusive application of an insecticide or fungicides often leads to selection of resistant microorganisms. Normally, such strains are also cross-resistant against other active ingredients having the same mode of action. An effective control of the pests and pathogens with said active ingredients is then not possible any longer. However, active ingredients having new mechanisms of action are difficult and expensive to develop.
The risk of resistance development in pest and pathogen populations as well as environmental and human health concerns have fostered interest in identifying alternatives to synthetic insecticides and fungicides for managing plant pests and diseases.
Natural insecticides are one approach for solving the above-mentioned problems. However, they are stille not entirely satisfactory.
Thus, there is a constant need for developing new, alternative plant protection agents which in some areas at least help to fulfill the above-mentioned requirements.
A known simulated natural pesticide is Requiem®, which contains a mixture of three terpenes, i.e. a- terpinene, p-cymene and limonene, as pesticidally active ingredients. It is disclosed in US 2010/0316738 corresponding to WO 2010/144919 and the references cited therein, which are incorporated herein by reference. WO 20120/144919 also discloses the use of the terpene mixture disclosed in this document in combination with one or more additional pesticidally active ingredients against plant pests, such as a carrier, a solvent or another pesticide such as another insecticide or biopesticide. Examples for additional pesticides which are disclosed in the document are fungicides, insecticides, miticides or acaricides, bactericides and the like as well as combinations thereof. The use of extracts comprising these three terpenes obtained from Chenopodium ambrosioides for controlling insect or mite infestation on plants is kown, including the use of such extracts that include natural terpenes isolated form Chenopodium. See e.g. US 2003/0091657 and US 2009/0030087, WO 2001/067868 and WO 2004/006679 and William Quarles (1192) Botanical Pesticides from Chenopodium, The IPM Practitioner Volume XIV, Number 2, 11 pages; and Lorenzo Sagero-Nieves (Mar/Apr 1995) Volatile Constituents from the Leaves of Chenopodium ambrosioides L., J. Essent. Oil Res. 7:221-223.
In view of this, it was in particular an object of the present invention to provide compositions which exhibit activity against insects, mites, nematodes and/or phytopathogens. Moreover, it was a further particular object of the present invention, to reduce the application rates and broaden the activity spectrum of the natural and synthetic insecticides, and thereby to provide a composition which, preferably at a reduced total amount of active ingredients applied, has improved activity against insects, mites, nematodes and/or phytopathogens. In particular, it was a further object of the present invention to provide a composition which, when applied to a crop, results in a decreased amount of residues in the crop, thereby reducing the risk of resistance formation and nevertheless provides efficient disease control.
Accordingly, it was found that these objects at least partly are solved by the compositions according to the invention as defined in the following. The composition according to the present invention preferably fulfills the above-described needs. It has been surprisingly discovered that the application of the composition according to the present invention in a simultaneous or sequential way to plants, plant parts, harvested fruits, vegetables and/or plant's locus of growth preferably allows better control of insects, mites, nematodes and/or phytopathogens than it is possible with the pesticidal terpene mixture on the one hand and with the individual synthetic insecticides on the other hand, alone (synergistic mixtures). By applying the pesticidal terpene mixture and the at least one insecticide according to the invention the activity against insects, mites, nematodes and/or phytopathogens is peferably increased in a superadditive manner.
As a consequence, the composition according to the present invention preferably allows a reduced total amount of active ingredients to be used and thus the crops which have been treated by this composition preferably show a decreased amount of residues in the crop. Accordingly, the risk of resistance formation of harmful microorganisms is decreased.
The present invention is directed to a composition comprising a pesticidal terpene mixture comprising the three terpenes a-terpinene, p-cymene and limonene, and optionally minor terpene ingredients and impurities, which are e.g. found in essential oil extracts from Chenopodium ambrosioides near ambrosioides such as thymol, carvacrol, carvone, carveol, and/or nerol, and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical.
Furthermore, the present invention relates to a kit of parts comprising the pesticidal terpene mixture comprising the three terpenes as mentioned before and at least one insecticde. The present invention is further directed to the use of said composition for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens.
Moreover, the present invention provides a method for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens.
Pesticidal terpene mixture
In general a "pesticidal" means the ability of a substance to increase mortality or inhibit the growth rate of plant pests. The term is used herein, to describe the property of a substance to exhibit activity against insects, mites, nematodes and/or phytopathogens. In the sense of the present invention the term "pests" include insects, mites, nematodes and/or phytopathogens.
The pesticidal terpene mixture of the invention comprises, as essential components, the terpenes a- terpinene, p-cymene and limonene.
The pesticidal mixture according to the invention may be obtained from any source such as, for example, as an extract from Chenopodium ambrosioides near ambrosioides, or as an extract from another plant genus/species that produces such terpenes, or produced synthetically (i.e. by a chemical synthesis process), and/or as a compound produced naturally by any organism (i.e. as a compound separate from an extract per se). The three terpenes may be from natural extracts obtained from Chenopodium ambrosioides near ambrosioides, or they are from natural analogs of such terpenes as extract from other plant species or other organisms. They may all three be synthetic versions of the terpenes obtainable from Chenopodium ambrosioides near ambrosioides or other plant species or other organisms. They may further be any possible combination of natural and/or synthetic versions of the three terpenes. Finally, the three terpenes can be obtained from any source or by any means except from an extract of Chenopodium ambrosioides near ambrosioides. Limonene exists in two enantiomeric forms, d- and 1-limonene, which are both included in the invention.
The pesticidal terpene mixture of the invention may, in a preferable embodiment, include only the essential oil extracts from or based on those found in Chenopodium ambrosioides near ambrosioides. It may aslo include only a synthetic blend simulating the essential oil extract from or based on those found in Chenopodium ambrosioides near ambrosioides. Further, it may include a mixture of the essential oil extract and the synthetic blend. It may be "normalized" by adding specific amounts of synthetic versions of one or more of the terpene compounds found in the natural extract and/or synthetic terpenes so as to produce a composition with a set ratio of the three terpenes.
More preferably, the pesticidal terpene mixture of the invention comprises the three substantially pure terpenes a-terpinene, p-cymene and limonene. Preferably, the pesticidal terpene mixture does not contain thymol, carvacrol, carvone, carveol (cis and trans), nerol and/or γ-terpinene, which are present in the extract from Chenopodium ambrosioides near ambrosioides at low levels. More preferably, the pesticidal terpene mixture does not contain said five terpenes and does not contain any other essential oils except those other essential oils that are present as minor impurities in the substantially pure a- terpinene, p-cymene and limonene. In the most preferred embodiment the pesticidal terpene mixture does not contain essential oils other than a-terpinene, p-cymene and limonene.
It is particularly preferred that the pesticidal terpene mixture of the invention does not comprise the bicyclic monoterpene ascaridole due to the mammalian toxicity of this compound which can be present in natural extracts from Chenopodium ambrosioides depending on the cultivar and the growing conditions.
In particular embodiments, the simulated blends in the above compositions are not from an extract of Chenopodium ambrosioides or from an extract of Chenopodium. In one embodiment, the pesticidally active compositions of the present invention only include the essential oil extracts from or based on those found in Chenopodium ambrosioides near ambrosioides. In another embodiment, the pesticidally active compositions ofthe present invention only include a synthetic blend simulating the essential oil extract from or based on those found in Chenopodium ambrosioides near ambrosioides. In another embodiment, the pesticidally active compositions of the present invention include a mixture of the essential oil extract and the synthetic blend. In some embodiments, the compositions to be applied to plants as a protectant are "normalized" by adding specific amounts of synthetic versions of one or more of the terpene compounds found in the natural extract and/or synthetic terpenes so as to produce a composition with a set ratio of the three terpenes, such as the ratio observed in certain standardized or preferred natural extracts from or based on those found in Chenopodium. In still other embodiments, the compositions used in the methods of the present invention are reconstituted, as explained more herein.
In some embodiments, the simulated blends simulating the Chenopodium extract consist essentially of natural analogs of such terpenes trom other plant species or other organisms, and/or the synthetic versions of such terpenes. In some embodiments, simulated blends comprise the three substantially pure α-terpinene, p-cymene and limonene, optionally with at least one volume filler that replaces the volume taken up by the minor components normally present in the extract of Chenopodium ambrosioides near ambrosioides.
In further embodiments, the simulated blends consist essentially of a-terpinene, p-cymene and limonene, and an oil wherein the a-terpinene, p-cymene and limonene are substantially pure and are not obtained from a Chenopodium extract, and wherein the excipient is not an essential oil.
In some embodiments the limonene is prepared from citrus peels or pines by cold press method.
The concentration of the α-terpinene in the pesticidal terpene mixture of the invention ranges from about 30 to about 70 %, preferably 35 % to 45 % and most preferably about 39 % by weight, the concentration of p-cymene in the pesticidal terpene mixture ranges from about 10 % to about 30 %, preferably from about 15 % to about 25 % and most preferably about 17 % by weight, and the concentration of limonene in the pesticidal terpene mixture ranges from about 1 % to about 20 %, preferably from about 5 % to about 15 % by weight and most preferably about 12 %, all based on the terpene mixture. In the most preferable embodiment of the invention, the absolute concentrations of α-terpinene is about 36 %, that of p-cymene is about 14.9 % and that of limonene is about 11.4 % by weight, all based on the pesticidal terpene mixture. Preferably, the relative ratio of α-terpinene, p-cymene and limonene in the pesticidal terpene mixture is 35-45 α-terpinene to about 12-20 p-cymene to about 10-15 limonene. Examples for preferable relative ratios of α-terpinene, p-cymene and limonene are 39: 17: 12, or about 40:15: 12, or about 36: 14.9: 11.4, or about 10.175:3.9:3.05. In some embodiments, the concentration of substantially pure α-terpinene in the compositions is about 39% by weight; the concentration of substantially pure p-cymene in the compositions is about 17% by weight, and the concentration of substantially pure limonene in the compositions is about 12%> by weight.
According to the invention the concentration of each pesticidally active terpene can be higher or lower than in the essential oil extract from Chenopodium ambrosioides near ambrosioides, but roughly maintaining the relative ratio to each others as in the essential oil extract.
The pesticidal terpene mixture of the invention can be obtained as an extract from Chenopodium ambrosioides near ambrosoides, as described in US 2009/0091657 and US 2009/0030087 as well as WO 2001/067868 and WO 2004/006679. It is also described in detail in US 61/213,470, US 61/246,872, US 61/247,885, US 61/256,257, US 61/286,314 and US 61/329,020, and it can be obtained as disclosed in US 2010/0316738 corresponding to WO 2012/14419. The disclosure of these documents is incorporated herein by reference. α-Terpinene, p-cymene and limonene are publicly available, can be produced synthetically using known methods or can be purified from various plant extracts according to methods generally known in the art. Further, all three of the terpenes are commercially available (e.g. Sigma- Aldrich®, Acros Organics, MP Biomedicals, Merck Chemicals). At least the following plant species produce a-terpinene: Anethum graceolens, Artemisia argyi, Cuminum cyminum, Elattaria cardamonum, Melaleuca alternifolia, Cardamom spp. and Origanum major ana.
At least the following plant species produce limonene, including d-limonene: Anethum graceolens, Anethum sowa, Carum carvi, Citrus, Foeniculum vulgare, Mentha piperita and Peppermint. Limonene may be obtained by steam distillation after alkali treatment of citrus peels and pulp, and also by fractionation of orange oil.
At least the following plant species produce p-cymene: Coridothymus sativum, Coridothymus captitatus, Cuminum cyminum, Origanum vulgare and Thymus vulgaris. Additional plants that produce the three terpenes are known in the art. Essential oils and/or certain fractions of essential oils (e.g. certain terpenes) can be extracted from a plant by distillation.
"Essential oils" means the volatile, aromatic oils obtained by steam or hydrodestillation of plant material and may include, but are not restricted to, being primarily composed of terpenes and their oxygenated derivatives. Essential oils can be obtained from, for example, flowers, leaves, seeds, roots, stems, bark, wood etc. Extraction and distillation methods of essential oils are known in the art.
A particularly preferable pesticidal terpene mixture of the invention is commercially available from the company AgroQuest under the trade name Requiem®. Preferably, this commercial product is used as pesticidal terpene mixture according to the invention. Besides the three terpenes a-terpinene, p-cymene and limonene, Requiem® contains excipients, solvents and other ingredients. In the following, all amounts of the "pesticidal terpene mixture of the invention" mentioned in commection with Requiem®, refer to the amount of the three terpenes contained in Requiem®, and not to the amount of the complete product Requiem®.
Insecticides
"Insecticides" as well as the term "insecticidal" refers to the ability of a substance to increase mortality or inhibit growth rate of insects. As used herein, the term "insects" includes all organisms in the class "Insecta". The term "pre-adult" insects refers to any form of an organism prior to the adult stage, including, for example, eggs, larvae, and nymphs.
"Nematicides" and "nematicidal" refers to the ability of a substance to increase mortality or inhibit the growth rate of nematodes. In general, the term "nematode" comprises eggs, larvae, juvenile and mature forms of said organism.
"Acaricide" and "acaricidal" refers to the ability of a substance to increase mortality or inhibit growth rate of ectoparasites belonging to the class Arachnida, sub-class Acari.
The insecticides specified herein by their "common name" are known and described, for example, in the Pesticide Manual ("The Pesticide Manual", 15th Ed., British Crop Protection Council 2009) or can be searched in the internet (e.g. http://www.alanwood.net/pesticides).
According to one embodiment of the present invention preferred insecticides are selected from the group consisting of
(1) Acetylcholinesterase (AChE) inhibitors, for example carbamates, e.g. Alanycarb (II), Aldicarb (12), Bendiocarb (13), Benfuracarb (14), Butocarboxim (15), Butoxycarboxim (16), Carbaryl (17), Carbofuran (18), Carbosulfan (19), Ethiofencarb (110), Fenobucarb (111), Formetanate (112), Furathiocarb (113), Isoprocarb (114), Methiocarb (115), Methomyl (116), Metolcarb (117), Oxamyl (118), Pirimicarb (119), Propoxur (120), Thiodicarb (121), Thiofanox (122), Triazamate (123), Trimethacarb (124), XMC (125), and Xylylcarb (126); or organophosphates, e.g. Acephate (127), Azamethiphos (128), Azinphos-ethyl (129), Azinphos-methyl (130), Cadusafos (131), Chlorethoxyfos (132), Chlorfenvinphos (133), Chlormephos (134), Chlorpyrifos (135), Chlorpyrifos-methyl (136), Coumaphos (137), Cyanophos (138), Demeton-S-methyl (139), Diazinon (140), Dichlorvos/DDVP (141), Dicrotophos (142), Dimethoate (143), Dimethylvinphos (144), Disulfoton (145), EPN (146), Ethion (147), Ethoprophos (148), Famphur (149), Fenamiphos (150), Fenitrothion (151), Fenthion (152), Fosthiazate (153), Heptenophos (154), Imicyafos (155), Isofenphos (156), Isopropyl O-(methoxyaminothio-phosphoryl) salicylate (157), Isoxathion (158), Malathion (159), Mecarbam (160), Methamidophos (161), Methidathion (162), Mevinphos (163), Monocrotophos (164), Naled (165), Omethoate (166), Oxydemeton-methyl (167), Parathion (168), Parathion-methyl (169), Phenthoate (170), Phorate (171), Phosalone (172), Phosmet (173), Phosphamidon (174), Phoxim (175), Pirimiphos-methyl (176), Profenofos (177), Propetamphos (178), Prothiofos (179), Pyraclofos (180), Pyridaphenthion (181), Quinalphos (182), Sulfotep (183), Tebupirimfos (184), Temephos (185), Terbufos (186), Tetrachlorvinphos (187), Thiometon (188), Triazophos (189), Trichlorfon (190), and Vamidothion (191); - -
(2) GABA-gated chloride channel antagonists, for example cyclodiene organochlorines, e.g. Chlordane (192) and Endosulfan (193); or phenylpyrazoles (fiproles), e.g. Ethiprole (194) and Fipronil (195);
(3) Sodium channel modulators / voltage-dependent sodium channel blockers, for example pyrethroids, e.g. Acrinathrin (196), Allethrin (197), d-cis-trans Allethrin (198), d-trans Allethrin (199), Bifenthrin
(1100), Bioallethrin (1101), Bioallethrin S-cyclopentenyl isomer (1102), Bioresmethrin (1103), Cycloprothrin (1104), Cyfluthrin (1105), beta-Cyfluthrin (1106), Cyhalothrin (1107), lambda-Cyhalothrin (1108), gamma-Cyhalothrin (1109), Cypermethrin (1110), alpha-Cypermethrin (II 11), beta-Cypermethrin (II 12), theta-Cypermethrin (II 13), zeta-Cypermethrin (II 14), Cyphenothrin [(lR)-trans isomers] (II 15), Deltamethrin (1116), Empenthrin [(EZ)-(IR) isomers) (1117), Esfenvalerate (1118), Etofenprox (1119), Fenpropathrin (1120), Fenvalerate (1121), Flucythrinate (1122), Flumethrin (1123), tau-Fluvalinate (1124), Halfenprox (1125), Imiprothrin (1126), Kadethrin (1127), Permethrin (1128), Phenothrin [(1R)- trans isomer) (1129), Prallethrin (1130), Pyrethrine (pyrethrum) (1131), Resmethrin (1132), Silafluofen (1133), Tefluthrin (1134), Tetramethrin (1135), Tetramethrin [(1R) isomers)] (1136), Tralomethrin (1137), and Transfluthrin (1138); or DDT (1139); or Methoxychlor (1140);
(4) Nicotinic acetylcholine receptor (nAChR) agonists, for example neonicotinoids, e.g. Acetamiprid (1141), Clothianidin (1142), Dinotefuran (1143), Imidacloprid (1144), Nitenpyram (1145), and Thiacloprid (1146), and Thiamethoxam (1147); or Nicotine (1148); or Sulfoxaflor (1149).
(5) Nicotinic acetylcholine receptor (nAChR) allosteric activators, for example spinosyns, e.g. Spinetoram (1150) and Spinosad (1151);
(6) Chloride channel activators, for example avermectins/milbemycins, e.g. Abamectin (1152), Emamectin benzoate (1153), Lepimectin (1154), and Milbemectin (1155);
(7) Juvenile hormone mimics, for example juvenile hormon analogues, e.g. Hydroprene (1156), Kinoprene (1157), and Methoprene (1158); or Fenoxycarb (1159); or Pyriproxyfen (1160); (8) Miscellaneous non-specific (multi-site) inhibitors, for example alkyl halides, e.g. Methyl bromide (1161) and other alkyl halides; or Chloropicrin (1162); or Sulfuryl fluoride (1163); or Borax (1164); or Tartar emetic (1165);
(9) Selective homopteran feeding blockers, e.g. Pymetrozine (1166); or Flonicamid (1167);
(10) Mite growth inhibitors, e.g. Clofentezine (1168), Hexythiazox (1169), and Diflovidazin (1170); or Etoxazole (I171); - -
(11) (11) Microbial disruptors of insect midgut membranes, e.g. Bacillus thuringiensis subspecies israelensis (1172), Bacillus thuringiensis subspecies aizawai (1173), Bacillus thuringiensis subspecies kurstaki (1174), Bacillus thuringiensis subspecies tenebrionis (1175), and B.t. Microbial disruptors of insect midgut membranes, e.g. B.t. crop proteins: CrylAb, CrylAc, CrylFa, CrylA.105, Cry2Ab, Vip3A, mCry3A, Cry3Ab, Cry3Bb, Cry34 Abl/35Abl (1176); or Bacillus sphaericus (1177);
(12) Inhibitors of mitochondrial ATP synthase, for example Diafenthiuron (1178); or organotin miticides, e.g. Azocyclotin (1179), Cyhexatin (1180), and Fenbutatin oxide (1181); or Propargite (1182); or Tetradifon (1183);
(13) Uncouplers of oxidative phoshorylation via disruption of the proton gradient, for example Chlorfenapyr (1184), DNOC (1185), and Sulfluramid (1186);
(14) Nicotinic acetylcholine receptor (nAChR) channel blockers, for example Bensultap (1187), Cartap hydrochloride (1188), Thiocyclam (1189), and Thiosultap-sodium (1190);
(15) Inhibitors of chitin biosynthesis, type 0, for example Bistrifluron (1191), Chlorfluazuron (1192), Diflubenzuron (1193), Flucycloxuron (1194), Flufenoxuron (1195), Hexaflumuron (1196), Lufenuron (1197), Novaluron (1198), Noviflumuron (1199), Teflubenzuron (1200), and Triflumuron (1201);
(16) Inhibitors of chitin biosynthesis, type 1, for example Buprofezin (1202);
(17) Moulting disruptors, for example Cyromazine (1203);
(18) Ecdysone receptor agonists, for example Chromafenozide (1204), Halofenozide (1205), Methoxyfenozide (1206), and Tebufenozide (1207); (19) Octopamine receptor agonists, for example Amitraz (1208);
(20) Mitochondrial complex III electron transport inhibitors, for example Hydramethylnon (1209); or Acequinocyl (1210); or Fluacrypyrim (1211);
(21) Mitochondrial complex I electron transport inhibitors, for example
METI acaricides, e.g. Fenazaquin (1212), Fenpyroximate (1213), Pyrimidifen (1214), Pyridaben (1215), Tebufenpyrad (1216), and Tolfenpyrad (1217); or Rotenone (Derris) (1218);
(22) Voltage-dependent sodium channel blockers, e.g. Indoxacarb (1219); or Metaflumizone (1220);
(23) Inhibitors of acetyl CoA carboxylase, for example tetronic and tetramic acid derivatives, e.g. Spirodiclofen (1221), Spiromesifen (1222), and Spirotetramat (1223); - -
(24) Mitochondrial complex IV electron transport inhibitors, for example phosphines, e.g. Aluminium phosphide (1224), Calcium phosphide (1225), Phosphine (1226), and Zinc phosphide (1227); or Cyanide (1228);
(25) Mitochondrial complex II electron transport inhibitors, for example beta-ketonitrile derivatives, e.g. Cyenopyrafen (1229) and Cyflumetofen (1230);
(28) Ryanodine receptor modulators, for example diamides, e.g. Chlorantraniliprole (1231), Cyantraniliprole (1232), and Flubendiamide (1233);
Further active ingredients with unknown or uncertain mode of action, for example Amidoflumet (1234), Azadirachtin (1235), Benclothiaz (1236), Benzoximate (1237), Bifenazate (1238), Bromopropylate (1239), Chinomethionat (1240), Cryolite (1241), Dicofol (1242), Diflovidazin (1243), Fluensulfone (1244), Flufenerim (1245), Flufiprole (1246), Fluopyram (1247), Fufenozide (1248), Imidaclothiz (1249), Iprodione (1250), Meperfluthrin (1251), Pyridalyl (1252), Pyrifluquinazon (1253), Tetramethylfluthrin (1254), and iodomethane (1255); furthermore products based on Bacillus firmus (including but not limited to strain CNCM 1-1582, such as, for example,VOTiVO™, BioNem) (1256) or one of the following known active ingredients: 3-bromo-N- {2-bromo-4-chloro-6-[(l-cyclopropyl- ethyl)carbamoyl]-phenyl}-l-(3-chloropyridin-2-yl)-lH-pyrazole-5-carboxamide (1257) (known from WO2005/077934), 4- {[(6-bromopyridin-3-yl)methyl](2-fluoroethyl)amino}furan-2(5H)-one (1258) (known from WO2007/115644), 4- {[(6-fluoropyridin-3-yl)methyl](2,2-difluoroethyl)amino}furan- 2(5H)-one (1259) (known from WO2007/115644), 4- {[(2-chloro-l,3-thiazol-5-yl)methyl](2- fluoroethyl)amino}furan-2(5H)-one (1260) (known from WO2007/115644), 4- {[(6-chlorpyridin-3- yl)methyl](2-fluoroethyl)amino}furan-2(5H)-one (1261) (known from WO2007/115644), Flupyradifurone (1262), 4- {[(6-chlor-5-fluoropyridin-3-yl)methyl](methyl)amino}-furan-2(5H)-one (1263) (known from WO2007/115643), 4- {[(5,6-dichloropyridin-3-yl)methyl](2- fluoroethyl)amino}furan-2(5H)-one (1264) (known from WO2007/115646), 4- {[(6-chloro-5- fluoropyridin-3-yl)methyl](cyclopropyl)amino}-furan-2(5H)-one (1265) (known from WO2007/115643), 4- {[(6-chloropyridin-3-yl)methyl](cyclopropyl)amino}furan-2(5H)-one (1266) (known from EP-A-0 539 588), 4- {[(6-chlorpyridin-3-yl)methyl](methyl)amino}furan-2(5H)-one (1267) (known from EP-A-0 539 588), {[l-(6-chloropyridin-3-yl)ethyl](methyl)oxido-λ4-sulfanylidene}- cyanamide (1268) (known from WO2007/149134) and its diastereomers {[(lR)-l-(6-chloropyridin-3- yl)ethyl](methyl)oxido-λ4-sulfanylidene}cyanamide (A) (1269), and {[(lS)-l-(6-chloropyridin-3- yl)ethyl](methyl)oxido-λ4-sulfanylidene}cyanamide (B) (1270) (also known from WO2007/149134) as well as diastereomers [(R)-methyl(oxido) {(lR)-l-[6-(trifluoromethyl)pyridin-3-yl]ethyl} -λ4- sulfanylidene]cyan-amide (Al) (1271), and [(S)-methyl(oxido) {(l S)-l -[6-(trifluoromethyl)pyridin-3- yl]ethyl}^4-sulfanylidene]cyanamide (A2) (1272), referred to as group of diastereomers A (known from WO2010/074747, WO2010/074751), [(R)-methyl(oxido) {(l S)-l -[6-(trifluoromethyl)pyridin-3- yl]ethyl}^4-sulfanylidene]-cyanamide (Bl) (1273), and [(S)-methyl(oxido) {(lR)-l-[6- - -
(trifluoromethyl) yridin-3-yl]ethyl}-λ4-sulfanylidene]cyanamide (B2) (1274), referred to as group of diastereomers B (also known from WO2010/074747, WO2010/074751), and 1 l-(4-chloro-2,6- dimethylphenyl)-12-hydroxy-l,4-dioxa-9-azadispiro[4.2.4.2]tetradec-l 1-en-lO-one (1275) (known from WO2006/089633), 3-(4'-fluoro-2,4-dimethylbiphenyl-3-yl)-4-hydroxy-8-oxa-l-azaspiro[4.5]dec-3-en-2- one (1276) (known from WO2008/067911), l- {2-fluoro-4-methyl-5-[(2,2,2- trifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH-l,2,4-triazol-5-amine (1277) (known from WO2006/043635), Afidopyropen [(3S,4aR,12R,12aS,12bS)-3-[(cyclopropylcarbonyl)oxy]-6,12- dihydroxy-4,12b-dimethyl 1-oxo-9-(pyridin-3-yl)-l,3,4,4a,5,6,6a,12,12a,12b-decahydro-2H,l lH- benzo[f]pyrano[4,3-b]chromen-4-yl]methyl cyclopropane-carboxylate (1278) (known from WO2008/066153), 2-cyano-3-(difluoromethoxy)-N,N-dimethylbenzenesulfonamide (1279) (known from WO2006/056433), 2-cyano-3-(difluoromethoxy)-N-methylbenzenesulfonamide (1280) (known from WO2006/100288), 2-cyano-3-(difluoromethoxy)-N-ethylbenzenesulfonamide (1281) (known from WO2005/035486), 4-(difluoromethoxy)-N-ethyl-N-methyl-l,2-benzothiazol-3 -amine 1,1-dioxide (1282) (known from WO2007/057407), N-[l -(2,3-dimethylphenyl)-2-(3,5-dimethylphenyl)ethyl]-4,5-dihydro- l,3-thiazol-2-amine (1283) (known from WO2008/104503), {l'-[(2E)-3-(4-chlorophenyl)prop-2-en-l- yl]-5-fluorospiro[indole-3,4'-piperidin]-l(2H)-yl}(2-chloropyridin-4-yl)methanone (1284) (known from WO2003/106457), 3-(2,5-dimethylphenyl)-4-hydroxy-8-methoxy-l,8-diazaspiro[4.5]dec-3-en-2-one (1285) (known from WO2009/049851), 3-(2,5-dimethylphenyl)-8-methoxy-2-oxo-l,8- diazaspiro[4.5]dec-3-en-4-yl ethyl carbonate (1286) (known from WO2009/049851), 4-(but-2-yn-l- yloxy)-6-(3,5-dimethylpiperidin-l-yl)-5-fluoropyrimidine (1287) (known from WO2004/099160), (2,2,3, 3,4,4,5, 5-octafluoropentyl)(3,3,3-trifluoropropyl)malononitrile (1288) (known from WO2005/063094), (2,2,3,3,4,4,5,5-octafluoropentyl)(3,3,4,4,4-pentafluoro-butyl)malononitrile (1289) (known from WO2005/063094), 8-[2-(cyclopropylmethoxy)-4-(trifluoromethyl)phenoxy]-3-[6- (trifluoromethyl)pyridazin-3-yl]-3-azabicyclo[3.2.1]octane (1290) (known from WO2007/040280), Flometoquin (1291), PF1364 (CAS-Reg.No. 1204776-60-2) (1292) (known from JP2010/018586), 5-[5- (3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-l ,2-oxazol-3-yl]-2-(lH-l,2,4-triazol-l- yl)benzonitrile (1293) (known from WO2007/075459), 5-[5-(2-chloropyridin-4-yl)-5-(trifluoromethyl)- 4,5-dihydro-l,2-oxazol-3-yl]-2-(lH-l,2,4-triazol-l-yl)benzo-nitrile (1294) (known from WO2007/075459), 4-[5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-l,2-oxazol-3-yl]-2- methyl-N- {2-oxo-2-[(2,2,2-trifluoro-ethyl)amino]ethyl}benzamide (1295) (known from WO2005/085216), 4- {[(6-chloropyridin-3-yl)methyl](cyclopropyl)amino} -l,3-oxazol-2(5H)-one (1296), 4- {[(6-chloropyridin-3-yl)methyl](2,2-difluoroethyl)amino}-l,3-oxazol-2(5H)-one (1297), 4- {[(6- chloropyridin-3-yl)methyl](ethyl)amino}-l,3-oxazol-2(5H)-one (1298), 4- {[(6-chloropyridin-3- yl)methyl](methyl)amino}-l,3-oxazol-2(5H)-one (1299) (all known from WO2010/005692), Pyflubumide N- [4-( 1 , 1 , 1 ,3 ,3 ,3 -hexafluoro-2-methoxypropan-2-yl)-3 -isobutylphenyl] -N-isobutyryl- l,3,5-trimethyl-lH-pyrazole-4-carboxamide (1300) (known from WO2002/096882), methyl 2-[2-({[3- bromo-l-(3-chloropyridin-2-yl)-lH-pyrazol-5-yl]carbonyl}amino)-5-chloro-3-methylbenzoyl]-2- methylhydrazinecarboxylate (1301) (known from WO2005/085216), methyl 2-[2-({[3-bromo-l-(3- - - chloropyridin-2-yl)-lH-pyrazol-5-yl]carbonyl}amino)-5-cyano-3-methylbenzoyl]-2- ethylhydrazinecarboxylate (1302) (known from WO2005/085216), methyl 2-[2-({[3-bromo-l-(3- chloropyridin-2-yl)-lH-pyrazol-5-yl]carbonyl}amino)-5-cyano-3-methylbenzoyl]-2- methylhydrazinecarboxylate (1303) (known from WO2005/085216), methyl 2-[3,5-dibromo-2-({[3- bromo- 1 -(3 -chloropyridin-2-yl)- 1 H-pyrazol-5-yl]carbonyl} amino)benzoyl]- 1 ,2-diethylhydrazine- carboxylate (1304) (known from WO2005/085216), methyl 2-[3,5-dibromo-2-({[3-bromo-l -(3- chloropyridin-2-yl)-lH-pyrazol-5-yl]carbonyl}amino)-benzoyl]-2-ethylhydrazinecarboxylate (1305) (known from WO2005/085216), (5RS,7RS;5RS,7SR)-l-(6-chloro-3-pyridylmethyl)-l,2,3,5,6,7- hexahydro-7-methyl-8-nitro-5-propoxyimidazo[l,2-a]pyridine (1306) (known from WO2007/101369), 2- {6-[2-(5-fluoropyridin-3-yl)-l,3-thiazol-5-yl]pyridin-2-yl}pyrimidine (1307) (known from WO2010/006713), 2- {6-[2-(pyridin-3-yl)-l,3-thiazol-5-yl]pyridin-2-yl}pyrimidine (1308) (known from WO2010/006713), l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)-lH-tetrazol-l-yl]methyl}-lH-pyrazole-5-carboxamide (1309) (known from WO2010/069502), l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)-2H-tetrazol-2-yl]methyl}-lH-pyrazole-5-carboxamide (1310) (known from WO2010/069502), N-[2-(tert-butylcarbamoyl)-4-cyano-6-methylphenyl]-l-(3-chloropyridin-2-yl)-3- {[5-(trifluoromethyl)-lH-tetrazol-l-yl]methyl} -lH-pyrazole-5-carboxamide (1311) (known from WO2010/069502), N-[2-(tert-butylcarbamoyl)-4-cyano-6-methylphenyl]-l-(3-chloropyridin-2-yl)-3- {[5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl} -lH-pyrazole-5-carboxamide (1312) (known from WO2010/069502), (lE)-N-[(6-chloropyridin-3-yl)methyl]-N'-cyano-N-(2,2-difluoroethyl)ethan- imidamide (1313) (known from WO2008/009360), N-[2-(5-amino-l,3,4-thiadiazol-2-yl)-4-chloro-6- methylphenyl]-3-bromo-l-(3-chloropyridin-2-yl)-lH-pyrazole-5-carboxamide (1314) (known from CN102057925), and methyl 2-[3,5-dibromo-2-({[3-bromo-l -(3-chloropyridin-2-yl)-lH-pyrazol-5- yl]carbonyl}amino)benzoyl]-2-ethyl-l-methylhydrazinecarboxylate (1315) (known from WO2011/049233).
In a preferred embodiment of the present invention the insecticide is a synthetic insecticide. As used herein, the term "synthetic" defines a compound that has not been obtained from a natural source such as a plant, bacterium or other organism.
According to a preferred embodiment of the present invention the insecticide is selected from the group consisting of Abamectin (1152) , Acephate (127), Acetamiprid (1141), Acrinathrin (196), Afidopyropen (1278), Alpha-Cypermethrin (II 11), Azadirachtin (1235), Bacillus firmus (1256), (Beta-Cyfluthrin (1106), Bifenthrin (1100), Buprofezin (1202), Clothianidin (1142), Chlorantraniliprole (1231), Chlorfenapyr (1184), Chlorpyrifos (135), Carbofuran (18), Cyantraniliprole (1232), Cyenopyrafen (1229), Cyflumentofen (1230), Cyfluthrin (1105), Cypermethrin (1110), Deltamethrin (1116), Diafenthiuron (1178), Dinotefuran (1143), Emamectin-benzoate (1153), Ethiprole (194), Fenpyroximate (1213), Fipronil (195), Flometoquin (1291), Flonicamid (1167), Flubendiamide (1233), Fluensulfone (1244), Fluopyram - -
(1247), Flupyradifurone (1262), Gamma-Cyhalothrin (1109), Imidacloprid (1144), Indoxacarb (1219), Lambda-Cyhalothrin (1108), Lufenuron (1197), Metaflumizone (1220), Methiocarb (115), Methoxyfenozide (1206), Milbemectin (1155), Profenofos (177), Pyflubumide (1300), Pymetrozine (1166), Pyrifluquinazone (1253), Spinetoram (1150), Spinosad (1151), Spirodiclofen (1221), Spiromesifen (1222), Spirotetramate (1223), Sulfoxaflor (1149), Tebufenpyrad (1216), Tefluthrin (1134), Thiacloprid (1146), Thiamethoxam (1147), Thiodicarb (121), Triflumuron (1201), l-(3-chloropyridin-2-yl)-N-[4- cyano-2-methyl-6-(methylcarbamoyl)phenyl] -3 - { [5 -(trifluoromethyl)- 1 H-tetrazol- 1 -yljmethyl} - 1 H- pyrazole-5-carboxamide (1309) (known from WO2010/069502), l-(3-chloropyridin-2-yl)-N-[4-cyano-2- methyl-6-(methylcarbamoyl)phenyl]-3- {[5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl} -lH-pyrazole-5- carboxamide (1310) (known from WO2010/069502) and l- {2-fluoro-4-methyl-5- [(2,2,2- trifluorethyl)sulfinyl]phenyl} -3 -(trifluoromethyl)- 1 H- 1 ,2,4-triazol-5-amine (1277), Afidopyropen (1278).
In a preferred ambodiment, the insecticide b) is selected from the group consisting of Abamectin (1152), Beta-Cyfluthrin (1-105), Clothianidin (1142), Chlorantraniliprole (1231), Cyantraniliprole (1232), Deltamethrin (1116), Fipronil (195), Flubendiamide (1233), Flupyradifurone (1262), Imidacloprid (1144), Methiocarb (1115), Sulfoxaflor (I149)Spinetoram (1150), Spinosad (1151), Spiromesifen (1222), Spirotetramate (1223), Tefluthrin (1134), Thiacloprid (1146), Thiamethoxam (1147), Thiodicarb (121), a mixture of l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)-2H-tetrazol-2-yl]methyl} - 1 H-pyrazole-5-carboxamide (1310) and 1 -(3-chloropyridin- 2-yl)-N- [4-cyano-2-methyl-6-(methylcarbamoyl)phenyl] -3 - { [5-(trifluoromethyl)- 1 H-tetrazol- 1 - yl]methyl}-lH-pyrazole-5-carboxamide (1309), and l- {2-fluoro-4-methyl-5- [(2,2,2- trifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH-l,2,4-triazol-5-amine (1277).
In one embodiment of the present invention, the insecticide, e.g. for seed treatment, is selected from the group consisting of Abamectin (1152), Carbofuran (18), Clothianidin (1142), Cyazypyr , Cycloxaprid, Cypermethrin (1110), Ethiprole (194), Fipronil (195), Fluopyram (1247), Imidacloprid (1144), Methiocarb (115), Rynaxypyr, Spinosad (1151), Sulfoxaflor (1149), Tefluthrin (1134), Thiametoxam (1147),
Thiodicarb (121).
In one embodiment of the present invention the composition comprises two or more insecticides. In a preferred embodiment the composition comprises two or more of the above-mentioned preferred insecticides. In particular, the preferred two or more insecticides are selected from the group consisting of Abamectin (1152) , Acephate (127), Acetamiprid (1141), Acrinathrin (196), Afidopyropen (1278), Alpha-Cypermethrin (1111), Azadirachtin (1235), Bacillus firmus, Beta-Cyfluthrin (1106), Bifenthrin (1100), Buprofezin (1202), Clothianidin (1142), Chlorantraniliprole (1231), Chlorfenapyr (1184), Chlorpyrifos (135), Carbofuran (18), Cyantraniliprole (1232), Cyenopyrafen (1229), Cyflumentofen (1230), Cyfluthrin (1105), Cypermethrin (1110), Deltamethrin (1116), Diafenthiuron (1178), Dinotefuran (1143), Emamectin-benzoate (1153), Ethiprole (194), Fenpyroximate (1213), Fipronil (195), Flometoquin (1291), Flonicamid (1167), Flubendiamide (1233), Fluensulfone (1244), Fluopyram (1247), - -
Flupyradifurone (1262), Gamma-Cyhalothrin (1109), Imidacloprid (1144), Indoxacarb (1219), Lambda- Cyhalothrin (1108), Lufenuron (1197), Metaflumizone (1220), Methiocarb (115), Methoxyfenozide (1206), Milbemectin (1155), Profenofos (177), Pyflubumide (1300), Pymetrozine (1166), Pyrifluquinazone (1253), Spinetoram (1150), Spinosad (1151), Spirodiclofen (1221), Spiromesifen (1222), Spirotetramate (1223), Sulfoxaflor (1149), Tebufenpyrad (1216), Tefluthrin (1134), Thiacloprid (1146), Thiamethoxam (1147), Thiodicarb (121), Triflumuron (1201), l-(3-chloropyridin-2-yl)-N-[4-cyano-2- methyl-6-(methylcarbamoyl)phenyl]-3- { [5-(trifluoromethyl)- 1 H-tetrazol- 1 -yl]methyl} - 1 H-pyrazole-5- carboxamide (1309) (known from WO2010/069502), l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6- (methylcarbamoyl)phenyl]-3 - { [5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl} - 1 H-pyrazole-5- carboxamide (1310) (known from WO2010/069502) and l- {2-fluoro-4-methyl-5- [(2,2,2- trifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH-l,2,4-triazol-5-amine (1277). In a particularaly preferred embodiment the insecticide b) is a mixture of 1309 and 1310.
Compositions according to the present invention
According to the present invention the composition comprises the pesticidal terpene mixture as defined above and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical.
A "synergistically effective amount" according to the present invention represents a quantitiy of a combination of the pesticidal terpene mixture and an insecticide that is statistically significantly more effective against insects, mites, nematodes and/or phytopatheogens than the pesticidal terpene mixture or the insecticide alone.
The term "synergistically effective amount" according to the invention is defined as follows:
The expected efficacy of a given combination of two compounds is calculated as follows (see Colby,
S.R., Calculating Synergistic and antagonistic Responses of Herbicide Combinations", Weeds 15, pp. 20-22, 1967): If
X is the efficacy expressed in % mortality of the untreated control for test compound A at a concentration of m ppm respectively m g/ha.
Y is the efficacy expressed in % mortality of the untreated control for test compound B at a concentration of n ppm respectively n g/ha. 5
E is the efficacy expressed in % mortality of the untreated control using the mixture
of A and B at m and n ppm respectively m and n g /ha, then is E = X + Y - fX » Y VI 00
If the observed insecticidal efficacy of the combination is higher than the one calculated as„E", then the combination of the two compounds is more than additive, i.e., there is a synergistic effect.
In a preferred embodiment the composition according to the present invention comprises the following combinations: In the following the designation Bl means the pesticidal terpene mixture according to the invention comprising a-terpinene, p-cymene and limonene as defined before.
Bl+Il, B1+I2, Bl+B, B1+I4, B1+I5, B1+I6, B1+I7, B1+I8, B1+I9, B1+B10, Bl+Il l, B1+I12, B1+I13, B1+I14, B1+I15, B1+I16, B1+I17, B1+I18, B1+I19, B1+I20, B1+I21, B1+ 122, B1+I23, B1+I24, B1+I25, B1+I26, B1+I27, B1+I28, B1+I29, B1+I30, B1+I31, B1+I32, B1+I33, B1+I34, B1+I35, B1+I36, B1+I37, B1+I38, B1+I39, B1+I40, B1+I41, B1+I42, B1+I43, B1+I44, B1+I45, B1+I46, B1+I47, B1+I48, B1+I49, B1+I50, B1+I51, B1+I52, B1+I53, B1+I54, B1+I55, B1+I56, B1+I57, B1+I58, B1+I59, B1+I60, B1+I61, B1+ 162, B1+I63, B1+I64, B1+I65, B1+I66, B1+I67, B1+I68, B1+I69, B1+I70, B1+I71, B1+I72, B1+I73, B1+I74, B1+I75, B1+I76, B1+I77, B1+I78, B1+I79, B1+I80, B1+I81, B1+I82, B1+I83, B1+I84, B1+I85, B1+I86, B1+I87, B1+I88, B1+I89, B1+I90, B1+I91, B1+I92, B1+I93, B1+I94, B1+I95, B1+I96, B1+I97, B1+I98, B1+I99, B1+I100, B1+I101, B1+I102, B1+I103, B1+I104, B1+I105, B1+I106, B1+I107, B1+I108, B1+I109, B1+I110, Bl+Il l l, B1+I112, B1+I113, B1+I114, B1+I115, B1+I116, B1+I117, B1+I118, B1+I119, B1+I120, B1+I121, B1+I122, B1+I123, B1+I124, B1+I125, B1+I126, B1+I127, B1+I128, B1+I129, B1+I130, B1+I131, B1+I132, B1+I133, B1+I134, B1+I135, B1+I136, B1+I137, B1+I138, B1+I139, B1+I140, B1+I141, B1+I142, B1+I143, B1+I144, B1+I145, B1+I146, B1+I147, B1+I148, B1+I149, B1+I150, B1+I151, B1+I152, B1+I153, B1+I154, B1+I155, B1+I156, B1+I157, B1+I158, B1+I159, B1+I160, B1+I161, B1+I162, B1+I163, B1+I164, B1+I165, B1+I168, B1+I169, B1+I170, B1+I171, B1+I172, B1+I173, B1+I174, B1+I175, B1+I176, B1+I177, B1+I178, B1+I179, B1+I180, B1+I181, B1+I182, B1+I183, B1+I184, B1+I185, B1+I186, B1+I187, B1+I188, B1+I189, B1+I190, B1+I191, B1+I192, B1+I193, B1+I194, B1+I195, B1+I196, B1+I197, B1+I198, B1+I199, B1+I200, B1+I201, B1+I202, B1+I203, B1+I204, B1+I205, B1+I206, B1+I207, B1+I208, B1+I209, B1+I210, B1+I211, B1+I212, B1+I213, B1+I214, B1+I215,B1+I216, B1+I217, B1+I218, B1+I219, B1+I220, B1+I221, B1+I222, B1+I223, B1+I224, B1+I225, B1+I226, B1+I227, B1+I228, B1+I229, B1+I230, B1+I231, B1+I232, B1+I233, Bl+1234, Bl+1235, Bl+1236, Bl+1237, Bl+1238, Bl+1239, Bl+1240, Bl+1241, Bl+1242, Bl+1243, B1+I244, B1+I245, B1+I246, B1+I247, B1+I248, B1+I249, B1+I250, B1+I251, B1+I252, B1+I253, B1+I254, B1+I255, B1+I257, B1+I258, B1+I259, B1+I260, B1+I261, B1+I262, B1+I263, B1+I264, B1+I265, B1+I266, B1+I267, B1+I268, B1+I269, B1+I270, B1+I271, B1+I272, B1+I273, B1+I274, - -
B1+I275, B1+I276, B1+I277, B1+I278, B1+I279, B1+I280, B1+I282, B1+I283, B1+I284, B1+I285, B1+I286, B1+I287, B1+I288, B1+I289, B1+I290, B1+I291, B1+I292, B1+I293, B1+I294, B1+I295, B1+I296, B1+I297, B1+I298, B1+I299, B1+I300, B1+I301, B1+I302, B1+I303, B1+I304, B1+I305, Β1+Γ306, B1+I307, B1+I308, B1+I309, B1+I310, B1+I311, B1+I312, B1+I313, B1+I314, B1+I315; In a highly preferred embodiment the present invention relates to a composition comprising the pesticidal terpene mixture as defined before and at least one insecticide selected from the group consisting of Abamectin, Acephate, Acetamiprid, Acrinathrin, Afidopyropen, Alpha-Cypermethrin, Azadirachtin, Bacillus firmus, Beta-Cyfluthrin, Bifenthrin, Buprofezin, Clothianidin, Chlorantraniliprole, Chlorfenapyr, Chlorpyrifos, Carbofuran, Cyantraniliprole, Cyenopyrafen, Cyflumentofen, Cyfluthrin, Cypermethrin, Deltamethrin, Diafenthiuron, Dinotefuran, Emamectin- benzoate, Ethiprole, Fenpyroximate, Fipronil, Flometoquin, Flonicamid, Flubendiamide, Fluensulfone, Fluopyram, Flupyradifurone, Gamma-Cyhalothrin, Imidacloprid, Indoxacarb, Lambda-Cyhalothrin, Lufenuron, Metaflumizone, Methiocarb, Methoxyfenozide, Milbemectin, Profenofos, Pyflubumide, Pymetrozine, Pyrifluquinazone, Spinetoram, Spinosad, Spirodiclofen, Spiromesifen, Spirotetramate, Sulfoxaflor, Tebufenpyrad, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, Triflumuron, l-(3- chloropyridin-2-yl)-N- [4-cyano-2-methyl-6-(methylcarbamoyl)phenyl] -3 - { [5 -(trifluoromethyl)- 1 H- tetrazol-l-yl]methyl}-lH-pyrazole-5-carboxamide, l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6- (methylcarbamoyl)phenyl]-3 - { [5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl} - 1 H-pyrazole-5- carboxamide, l- {2-fluoro-4-methyl-5-[(2,2,2 rifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH- l,2,4-triazol-5-amine in a synergistically effective amount.
More preferably, the composition comprises Requiem® and an insecticide b) selected from the group consisting of Abamectin, Beta-Cyfluthrin, Clothianidin, Chlorantraniliprole, Cyantraniliprole, Deltamethrin, Fipronil, Flubendiamide, Flupyradifurone, Imidacloprid, Methiocarb, Spinetoram, Spinosad, Spiromesifen, Spirotetramate, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, a mixture of l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5-(trifluoromethyl)- 2H-tetrazol-2-yl]methyl} -lH-pyrazole-5-carboxamide and l-(3-chloropyridin-2-yl)-N-[4-cyano-2- methyl-6-(methylcarbamoyl)phenyl]-3- { [5-(trifluoromethyl)- 1 H-tetrazol- 1 -yljmethyl} - 1 H-pyrazole-5- carboxamide, and l- {2-fluoro-4-methyl-5-[(2,2,2 rifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH- 1 ,2,4-triazol-5-amine. In particular, the composition according to the invention does not comprise citrus oil as single second insecticide.
Further, the compositions of the inventions are not the following combinations: - Pesticidal terpene mixture and Ν,Ν-diethyl-toluamide (Autan®) ?
- Pesticidal terpene mixture and Flonicamide (e.g. Beleaf®), as disclosed on page 47, 1. 22 of WO
2012/144919
- Pesticidal terpene mixture and Pymetrozine (e.g. Fulfill®), as disclosed on page 47, 1. 22 of WO
2012/144919 - Pesticidal terpene mixture and Spiromesifen (Oberon®), in particular the sequential use of the terpene mixture and Spiromesifen (Oberon®), as disclosed in Example 15 of US 2012/0316738
- Pesticidal terpene mixture and Imidacloprid (Admire®), Pymetrozine (Fulfill®) and Spiromesifen
(Oberon®), as disclosed in Table 14 of WO 20120/144919
- Pesticidal terpene mixture and Imidacloprid (Admire®), Pymetrozine (Fulfill®), Spirotetramat (Movento®) and Spiromesifen (Oberon®), as disclosed in Table 14 of WO 20120/144919
Further, the invention does not include
- the sequential treatment, in particular of watermelon seedlings, comprising separate treatment with the pesticidal terpene mixture of the invention and the specific insecticides/fungicides 2x Pymetrozine (Fulfill®), 2x Endosulfan (Thionex®), 2x Spiromesifen (Oberon®), 2x Endosulfan (Thionex®), as disclosed in Example 5 of WO 20120/144919,
- the sequential treatment, in particular of S. tuberosum, using the pesticidal terpene mixture of the invention every 3 to 4 days and the standard grower sequence using Acetamipirid (Assail®), Flonicamid (Beleaf®), Pymetrozine (Fulfill®), Imidacloprid (Provado®), Acetamipirid (Assail®), Methamidophos (Monitor®), as disclosed in Example 6 of US 2012/0316738 - the sequential treatment, in particular of "Jalapeno" pepper transplants, using the pesticidal terpene mixture of the invention and Spinetoram-J and Spinetoram-L (Radiant®) disclosed in Example 14 of US 2012/0316738
WO 20120/144919 discloses combiantions of the pesticidal terpene mixture with 2-ethyl-l,3- hexanediol, N-octyl bicycloheptene dicarboxamide, N,N-diethyl-M-toluamide, 2,3:4,5-Bis (2-butylene) tetrahydro-2-furaldehyde, Di-n-propyl isocinchomeronate, 2-hydroxyethyl-n-octyl sulfide. These compounds are described in WO 20120/144919 as "other repellents". However, the present inventors consider them merely formulation aids. Anyway, combinations of the pestcicidal terpene mixture with these compounds are excluded from the present invention.
In a preferred embodiment of the present invention the composition further comprises at least one fungicide with the proviso that the pesticidal terpene mixture and the fungicide are not identical. The term "active ingredient" is used in the present description to designate the pestcidal terpene mixture, the insecticide and the fungicide.
Fungicides
In general, "fungicidal" means the ability of a substance to increase mortality or inhibit the growth rate of fungi.
The term "fungus" or "fungi" includes a wide variety of nucleated sporebearing organisms that are devoid of chlorophyll. Examples of fungi include yeasts, molds, mildews, rusts, and mushrooms.
According to one embodiment of the present invention preferred fungicides are selected from the group consisting of
(1) Inhibitors of the ergosterol biosynthesis, for example (Fl) aldimorph (1704-28-5), (F2) azaconazole (60207-31-0), (F3) bitertanol (55179-31-2), (F4) bromuconazole (116255-48-2), (F5) cyproconazole (113096-99-4), (F6) diclobutrazole (75736-33-3), (F7) difenoconazole (119446-68-3), (F8) diniconazole (83657-24-3), (F9) diniconazole-M (83657-18-5), (F10) dodemorph (1593-77-7), (Fl l) dodemorph acetate (31717-87-0), (F12) epoxiconazole (106325-08-0), (F13) etaconazole (60207-93-4), (F14) fenarimol (60168-88-9), (F15) fenbuconazole (114369-43-6), (F16) fenhexamid (126833-17-8), (F17) fenpropidin (67306-00-7), (F18) fenpropimorph (67306-03-0), (F19) fluquinconazole (136426-54-5), (F20) flurprimidol (56425-91-3), (F21) flusilazole (85509-19-9), (F22) flutriafol (76674-21-0), (F23) furconazole (112839-33-5), (F24) furconazole-cis (1 12839-32-4), (F25) hexaconazole (79983-71-4), (F26) imazalil (60534-80-7), (F27) imazalil sulfate (58594-72-2), (F28) imibenconazole (86598-92-7), (F29) ipconazole (125225-28-7), (F30) metconazole (125116-23-6), (F31) myclobutanil (88671-89-0), (F32) naftifme (65472-88-0), (F33) nuarimol (63284-71-9), (F34) oxpoconazole (174212-12-5), (F35) paclobutrazol (76738-62-0), (F36) pefurazoate (101903-30-4), (F37) penconazole (66246-88-6), (F38) piperalin (3478-94-2), (F39) prochloraz (67747-09-5), (F40) propiconazole (60207-90-1), (F41) prothioconazole (178928-70-6), (F42) pyributicarb (88678-67-5), (F43) pyrifenox (88283-41-4), (F44) quinconazole (103970-75-8), (F45) simeconazole (149508-90-7), (F46) spiroxamine (118134-30-8), (F47) tebuconazole (107534-96-3), (F48) terbinafme (91161-71-6), (F49) tetraconazole (112281-77-3), (F50) triadimefon (43121-43-3), (F51) triadimenol (89482-17-7), (F52) tridemorph (81412-43-3), (F53) triflumizole (68694-11-1), (F54) triforine (26644-46-2), (F55) triticonazole (131983-72-7), (F56) uniconazole (83657-22-1), (F57) uniconazole-p (83657-17-4), (F58) viniconazole (77174-66-4), (F59) voriconazole (137234-62-9), (F60) l-(4-chlorophenyl)-2-(lH-l,2,4-triazol-l-yl)cycloheptanol (129586- 32-9), (F61) methyl l-(2,2-dimethyl-2,3-dihydro-lH-inden-l -yl)-lH-imidazole-5-carboxylate (110323- 95-0), (F62) N'- {5-(difluoromethyl)-2-methyl-4-[3-(trimethylsilyl)propoxy]phenyl} -N-ethyl-N- methylimidoformamide, (F63) N-ethyl-N-methyl-N'- {2-methyl-5-(trifluoromethyl)-4-[3- - -
(trimethylsilyl)propoxy] -phenyl} -imidoformamide, (F64) 0-[l-(4-methoxyphenoxy)-3,3-dimethylbutan- 2-yl] lH-imidazole-l-carbothioate (111226-71-2);
(2) inhibitors of the respiratory chain at complex I or II, for example (F65) bixafen (581809-46-3), (F66) boscalid (188425-85-6), (F67) carboxin (5234-68-4), (F68) diflumetorim (130339-07-0), (F69) fenfuram (24691-80-3), (F70) fluopyram (658066-35-4), (F71) flutolanil (66332-96-5), (F72) fluxapyroxad (907204-31-3), (F73) furametpyr (123572-88-3), (F74) furmecyclox (60568-05-0), (F75) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR) (881685- 58-1), (F76) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (F77) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (F78) isopyrazam (anti-epimeric enantiomer 1 S,4R,9R), (F79) isopyrazam (syn epimeric racemate 1RS,4SR,9RS), (F80) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (F81) isopyrazam (syn-epimeric enantiomer 1 S,4R,9S), (F82) mepronil (55814-41-0), (F83) oxycarboxin (5259-88-1), (F84) penflufen (494793-67-8), (F85) penthiopyrad (183675-82-3), (F86) sedaxane (874967-67-6), (F87) thifluzamide (130000-40-7), (F88) l-methyl-N-[2-(l , 1,2,2- tetrafluoroethoxy)phenyl]-3-(trifluoromethyl)-lH-pyrazole-4-carboxamide, (F89) 3-(difluoromethyl)-l- methyl-N-[2-(l ,l,2,2-tetrafluoroethoxy)phenyl]-lH-pyrazole-4-carboxamide, (F90) 3-(difluoromethyl)- N-[4-fluoro-2-(l ,l, 2,3,3, 3 -hexafluoropropoxy)phenyl]-l -methyl- lH-pyrazole-4-carboxamide, (F91) N- [ 1 -(2,4-dichlorophenyl)- 1 -methoxypropan-2-yl] -3 -(difluoromethyl)- 1 -methyl- 1 H-pyrazole-4- carboxamide (1092400-95-7), (F92) 5,8-difluoro-N-[2-(2-fluoro-4- {[4-(trifluoromethyl)pyridin-2- yl]oxy}phenyl)ethyl]-quinazolin-4-amine (1210070-84-0), (F93) benzovindiflupyr, (F94) N-[(lS,4R)-9- (dichloromethylene)- 1 ,2,3 ,4-tetrahydro- 1 ,4-methanonaphthalen-5-yl] -3 -(difluoromethyl)- 1 -methyl- 1 H- pyrazole-4-carboxamide, (F95) N-[(lR,4S)-9-(dichloromethylene)-l,2,3,4-tetrahydro-l,4- methanonaphthalen-5-yl] -3 -(difluoromethyl)- 1 -methyl- 1 H-pyrazole-4-carboxamide, (F96) 3 - (Difluormethyl)- 1 -methyl-N-( 1 , 1 ,3 -trimethyl-2,3 -dihydro- 1 H-inden-4-yl)- 1 H-pyrazol-4-carboxamid, (F97) l,3,5-Trimethyl-N-(l ,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (F98) l-Methyl-3-(trifluormethyl)-N-(l ,3,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH-pyrazol-4-carboxamid, (F99) 1 -Methyl-3 -(trifluormethyl)-N- [(1S)-1 ,3 ,3 -trimethyl-2,3 -dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4- carboxamid, (F 100) 1 -Methyl-3 -(trifluormethyl)-N- [( 1 R)- 1 ,3 ,3 -trimethyl-2,3 -dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid, (F 101 ) 3 -(Difluormethyl)- 1 -methyl-N- [(3 S)- 1 , 1 ,3 -trimethyl-2,3 -dihydro- 1 H- inden-4-yl]-lH-pyrazol-4-carboxamid, (F102) 3-(Difluormethyl)-l-methyl-N-[(3R)-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl]-lH-pyrazol-4-carboxamid, (F103) l,3,5-Trimethyl-N-[(3R)-l,l,3-trimethyl-2,3- dihydro-lH-inden-4-yl]-lH-pyrazol-4-carboxamid, (F104) l,3,5-Trimethyl-N-[(3S)-l,l,3-trimethyl-2,3- dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid;
(3) inhibitors of the respiratory chain at complex III, for example (F105) ametoctradin (865318-97-4), (F106) amisulbrom (348635-87-0), (F107) azoxystrobin (131860-33-8), (F108) cyazofamid (120116-88- 3), (F109) coumethoxystrobin (850881-30-0), (F110) coumoxystrobin (850881-70-8), (Fi l l) dimoxystrobin (141600-52-4), (F112) enestroburin (238410-11-2), (F113) famoxadone (131807-57-3), - -
(F114) fenamidone (161326-34-7), (F115) fenoxystrobin (918162-02-4), (F116) fluoxastrobin (361377- 29-9), (F117) kresoxim-methyl (143390-89-0), (F118) metominostrobin (133408-50-1), (F119) orysastrobin (189892-69-1), (F120) picoxystrobin (1 17428-22-5), (F121) pyraclostrobin (175013-18-0), (F122) pyrametostrobin (915410-70-7), (F123) pyraoxystrobin (862588-11-2), (F124) pyribencarb (799247-52-2), (F125) triclopyricarb (902760-40-1), (F126) trifloxystrobin (141517-21-7), (F127) (2E)-
2- (2- {[6-(3-chloro-2-methylphenoxy)-5-fluoropyrimidin-4-yl]oxy}phenyl)-2-(methoxyimino)-N- methylethanamide, (F 128) (2E)-2-(methoxyimino)-N-methyl-2-(2- { [( {(1 E)- 1 - [3- (trifluoromethyl)phenyl] ethylidene } amino) oxy] methyl } phenyl)ethanamide, (F 129) (2E) -2- (methoxyimino)-N-methyl-2- {2-[(E)-( { 1 -[3-(trifluoromethyl)phenyl]ethoxy} - imino)methyl]phenyl}ethanamide (158169-73-4), (F130) (2E)-2- {2-[( {[(lE)-l -(3- {[(E)-l-fluoro-2- phenylethenyl] oxy } phenyl)ethylidene] amino } oxy)methyl]phenyl} -2-(methoxyimino)-N- methylethanamide (326896-28-0), (F131) (2E)-2- {2-[({[(2E,3E)-4-(2,6-dichlorophenyl)but-3-en-2- ylidene] amino} oxy)methyl] phenyl} -2-(methoxy-imino)-N-methylethanamide, (Fl 32) 2-chloro-N- (l ,l,3-trimethyl-2,3-dihydro-lH-inden-4-yl)pyridine-3-carboxamide (119899-14-8), (F133) 5-methoxy- 2-methyl-4-(2- {[( {(lE)-l-[3-(trifluoromethyl)phenyl]ethylidene}amino)oxy]methyl}phenyl)-2,4- dihydro-3H-l,2,4-triazol-3-one, (F134) methyl (2E)-2- {2-[({cyclopropyl[(4- methoxyphenyl)imino]methyl}sulfanyl)methyl]phenyl}-3-methoxyprop-2-enoate (149601-03-6), (F135) N-(3-ethyl-3,5,5-trimethylcyclohexyl)-3-(formylamino)-2-hydroxybenzamide (226551-21-9), (F136) 2- {2-[(2,5-dimethylphenoxy)methyl]-phenyl} -2-methoxy-N-methylacetamide (173662-97-0), (Fl 37) (2R)-2- {2-[(2,5-dimethylphenoxy)methyl]phenyl} -2-methoxy-N-methylacetamide (394657-24-0);
(4) Inhibitors of the mitosis and cell division, for example (F138) benomyl (17804-35-2), (F139) carbendazim (10605-21-7), (F140) chlorfenazole (3574-96-7), (F141) diethofencarb (87130-20-9), (F142) ethaboxam (162650-77-3), (F143) fluopicolide (239110-15-7), (F144) fuberidazole (3878-19-1), (F145) pencycuron (66063-05-6), (F146) thiabendazole (148-79-8), (F147) thiophanate-methyl (23564- 05-8), (F148) thiophanate (23564-06-9), (F149) zoxamide (156052-68-5), (F150) 5-chloro-7-(4- methylpiperidin-l-yl)-6-(2,4,6-trifluorophenyl)[l,2,4]triazolo[l,5-a]pyrimidine (214706-53-3), (F151)
3- chloro-5-(6-chloropyridin-3-yl)-6-methyl-4-(2,4,6-trifluoro-phenyl)pyridazine (1002756-87-7);
(5) Compounds capable to have a multisite action, like for example (F152) bordeaux mixture (8011-63-
0) , (F153) captafol (2425-06-1), (F154) captan (133-06-2), (F155) chlorothalonil (1897-45-6), (F156) copper hydroxide (20427-59-2), (F157) copper naphthenate (1338-02-9), (F158) copper oxide (1317-39-
1) , (F159) copper oxychloride (1332-40-7), (F160) copper(2+) sulfate (7758-98-7), (F161) dichlofluanid (1085-98-9), (F162) dithianon (3347-22-6), (F163) dodine (2439-10-3), (F164) dodine free base, (F165) ferbam (14484-64-1), (F166) fluorofolpet (719-96-0), (F167) folpet (133-07-3), (F168) guazatine (108173-90-6), (F169) guazatine acetate, (F170) iminoctadine (13516-27-3), (F171) iminoctadine albesilate (169202-06-6), (F172) iminoctadine triacetate (57520-17-9), (F173) mancopper (53988-93-5), (F174) mancozeb (8018-01-7), (F175) maneb (12427-38-2), (F176) metiram (9006-42-2), (F177) - - metiram zinc (9006-42-2), (F178) oxine-copper (10380-28-6), (F179) propamidine (104-32-5), (F180) propineb (12071-83-9), (F 181 ) sulphur and sulphur preparations including calcium polysulphide (7704- 34-9), (F182) thiram (137-26-8), (F183) tolylfluanid (731-27-1), (F184) zineb (12122-67-7), (F185) ziram (137-30-4); (6) Compounds capable to induce a host defence, like for example (F186) acibenzolar-S-methyl (135158-54-2), (F187) isotianil (224049-04-1), (F188) probenazole (27605-76-1), (F189) tiadinil (223580-51-6);
(7) Inhibitors of the amino acid and/or protein biosynthesis, for example (F190) andoprim (23951 -85-1), (F191) blasticidin-S (2079-00-7), (F192) cyprodinil (121552-61-2), (F193) kasugamycin (6980-18-3), (F194) kasugamycin hydrochloride hydrate (19408-46-9), (F195) mepanipyrim (110235-47-7), (F196) pyrimethanil (53112-28-0), (F197) 3-(5-fluoro-3,3,4,4-tetramethyl-3,4-dihydroisoquinolin-l- yl)quinoline (861647-32-7);
(8) Inhibitors of the ATP production, for example (F198) fentin acetate (900-95-8), (F199) fentin chloride (639-58-7), (F200) fentin hydroxide (76-87-9), (F201) silthiofam (175217-20-6); (9) Inhibitors of the cell wall synthesis, for example (F202) benthiavalicarb (177406-68-7), (F203) dimethomorph (110488-70-5), (F204) flumorph (211867-47-9), (F205) iprovalicarb (140923-17-7), (F206) mandipropamid (374726-62-2), (F207) polyoxins (11113-80-7), (F208) polyoxorim (22976-86- 9), (F209) validamycin A (37248-47-8), (F210) valifenalate (283159-94-4; 283159-90-0);
(10) Inhibitors of the lipid and membrane synthesis, for example (F211) biphenyl (92-52-4), (F212) chloroneb (2675-77-6), (F213) dicloran (99-30-9), (F214) edifenphos (17109-49-8), (F215) etridiazole (2593-15-9), (F216) iodocarb (55406-53-6), (F217) iprobenfos (26087-47-8), (F218) isoprothiolane (50512-35-1), (F219) propamocarb (25606-41-1), (F220) propamocarb hydrochloride (25606-41-1), (F221) prothiocarb (19622-08-3), (F222) pyrazophos (13457-18-6), (F223) quintozene (82-68-8), (F224) tecnazene (117-18-0), (F225) tolclofos-methyl (57018-04-9); (11) Inhibitors of the melanine biosynthesis, for example (F226) carpropamid (104030-54-8), (F227) diclocymet (139920-32-4), (F228) fenoxanil (115852-48-7), (F229) phthalide (27355-22-2), (F230) pyroquilon (57369-32-1), (F231) tricyclazole (41814-78-2), (F232) 2,2,2-trifluoroethyl {3-methyl-l -[(4- methylbenzoyl)amino] -butan-2-yl} carbamate (851524-22-6);
(12) Inhibitors of the nucleic acid synthesis, for example (F233) benalaxyl (71626-11-4), (F234) benalaxyl-M (kiralaxyl) (98243-83-5), (F235) bupirimate (41483-43-6), (F236) clozylacon (67932-85- 8), (F237) dimethirimol (5221-53-4), (F238) ethirimol (23947-60-6), (F239) furalaxyl (57646-30-7), (F240) hymexazol (10004-44-1), (F241) metalaxyl (57837-19-1), (F242) metalaxyl-M (mefenoxam) - -
(70630-17-0), (F243) ofurace (58810-48-3), (F244) oxadixyl (77732-09-3), (F245) oxolinic acid (14698-29-4);
(13) Inhibitors of the signal transduction, for example (F246) chlozolinate (84332-86-5), (F247) fenpiclonil (74738-17-3), (F248) fludioxonil (131341-86-1), (F249) iprodione (36734-19-7), (F250) procymidone (32809-16-8), (F251) quinoxyfen (124495-18-7), (F252) vinclozolin (50471-44-8);
(14) Compounds capable to act as an uncoupler, like for example (F253) binapacryl (485-31-4), (F254) dinocap (131-72-6), (F255) ferimzone (89269-64-7), (F256) fluazinam (79622-59-6), (F257) meptyldinocap (131-72-6);
(15) Further compounds, like for example (F258) benthiazole (21564-17-0), (F259) bethoxazin (163269- 30-5), (F260) capsimycin (70694-08-5), (F261) carvone (99-49-0), (F262) chinomethionat (2439-01-2),
(F263) pyriofenone (chlazafenone) (688046-61-9), (F264) cufraneb (11096-18-7), (F265) cyflufenamid (180409-60-3), (F266) cymoxanil (57966-95-7), (F267) cyprosulfamide (221667-31-8), (F268) dazomet (533-74-4), (F269) debacarb (62732-91-6), (F270) dichlorophen (97-23-4), (F271) diclomezine (62865- 36-5), (F272) difenzoquat (49866-87-7), (F273) difenzoquat methylsulphate (43222-48-6), (F724) diphenylamine (122-39-4), (F275) ecomate, (F276) fenpyrazamine (473798-59-3), (F277) flumetover (154025-04-4), (F278) fluoroimide (41205-21-4), (F279) flusulfamide (106917-52-6), (F280) flutianil (304900-25-2), (F281) fosetyl-aluminium (39148-24-8), (F282) fosetyl-calcium, (F283) fosetyl-sodium (39148-16-8), (F284) hexachlorobenzene (118-74-1), (F285) irumamycin (81604-73-1), (F286) methasulfocarb (66952-49-6), (F287) methyl isothiocyanate (556-61-6), (F288) metrafenone (220899- 03-6), (F289) mildiomycin (67527-71-3), (F290) natamycin (7681-93-8), (F291) nickel dimethyl- dithiocarbamate (15521-65-0), (F292) nitrothal-isopropyl (10552-74-6), (F293) octhilinone (26530-20- 1), (F294) oxamocarb (917242-12-7), (F295) oxyfenthiin (34407-87-9), (F296) pentachlorophenol and salts (87-86-5), (F297) phenothrin, (F298) phosphorous acid and its salts (13598-36-2), (F299) propamocarb-fosetylate, (F300) propanosine-sodium (88498-02-6), (F301) proquinazid (189278-12-4), (F302) pyrimorph (868390-90-3), (F303) (2E)-3-(4-tert-butylphenyl)-3-(2-chloropyridin-4-yl)-l- (morpholin-4-yl)prop-2-en-l -one (1231776-28-5), (F304) (2Z)-3-(4-tert-butylphenyl)-3-(2- chloropyridin-4-yl)-l-(morpholin-4-yl)prop-2-en-l-one (1231776-29-6), (F305) pyrrolnitrine (1018-71- 9), (F306) tebufloquin (376645-78-2), (F307) tecloftalam (76280-91-6), (F308) tolnifanide (304911-98- 6), (F309) triazoxide (72459-58-6), (F310) trichlamide (70193-21-4), (F311) zarilamid (84527-51-5), (F312) (3S,6S,7R,8R)-8-benzyl-3-[( {3-[(isobutyryloxy)methoxy]-4-methoxypyridin-2- yl}carbonyl)amino]-6-methyl-4,9-dioxo-l,5-dioxonan-7-yl 2-methylpropanoate (517875-34-2), (F313) l-(4- {4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l-yl)-2-[5- methyl-3-(trifluoromethyl)-lH-pyrazol-l -yl]ethanone (1003319-79-6), (F314) l-(4- {4-[(5S)-5-(2,6- difluorophenyl)-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l -yl)-2-[5-methyl-3- (trifluoromethyl)-lH-pyrazol-l-yl]ethanone (1003319-80-9), (F315) l-(4- {4-[5-(2,6-difluorophenyl)- 4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l-yl)-2-[5-methyl-3-(trifluoro-methyl)-lH- - - pyrazol-l-yl]ethanone (1003318-67-9), (F316) l-(4-methoxyphenoxy)-3,3-dimethylbutan-2-yl 1H- imidazole-l-carboxylate (111227-17-9), (F317) 2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine (13108- 52-6), (F318) 2,3-dibutyl-6-chlorothieno[2,3-d]pyrimidin-4(3H)-one (221451-58-7), (F319) 2,6- dimethyl-lH,5H-[l,4]dithiino[2,3-c:5,6-c']dipyrrole-l,3,5,7(2H,6H)-tetrone, (F320) 2-[5-methyl-3- (trifluoromethyl)-lH-pyrazol-l-yl]-l-(4- {4-[(5R)-5-phenyl-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2- yl}piperidin-l -yl)ethanone (1003316-53-7), (F321) 2-[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l-yl]-l- (4- {4-[(5S)-5-phenyl-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l -yl)ethanone (1003316- 54-8), (F322) 2-[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l-yl]-l- {4-[4-(5-phenyl-4,5-dihydro-l,2- oxazol-3-yl)-l,3-thiazol-2-yl]piperidin-l-yl}ethanone (1003316-51-5), (F323) 2-butoxy-6-iodo-3- propyl-4H-chromen-4-one, (F324) 2-chloro-5-[2-chloro- 1 -(2,6-difluoro-4-methoxyphenyl)-4-methyl- lH-imidazol-5-yl]pyridine, (F325) 2-phenylphenol and salts (90-43-7), (F326) 3-(4,4,5-trifluoro-3,3- dimethyl-3,4-dihydroisoquinolin-l-yl)quinoline (861647-85-0), (F327) 3,4,5-trichloropyridine-2,6- dicarbonitrile (17824-85-0), (F328) 3-[5-(4-chlorophenyl)-2,3-dimethyl-l,2-oxazolidin-3-yl]pyridine, (F329) 3-chloro-5-(4-chlorophenyl)-4-(2,6-difluorophenyl)-6-methylpyridazine, (F330) 4-(4- chlorophenyl)-5-(2,6-difluorophenyl)-3,6-dimethylpyridazine, (F331) 5-amino-l,3,4-thiadiazole-2-thiol, (F332) 5-chloro-N'-phenyl-N'-(prop-2-yn-l -yl)thiophene-2-sulfonohydrazide (134-31-6), (F333) 5- fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine (1174376-11-4), (F334) 5-fluoro-2-[(4- methylbenzyl)oxy]pyrimidin-4-amine (1174376-25-0), (F335) 5-methyl-6-octyl[l,2,4]triazolo[l,5- a]pyrimidin-7-amine, (F336) ethyl (2Z)-3-amino-2-cyano-3-phenylprop-2-enoate, (F337) N'-(4- {[3-(4- chlorobenzyl)-l,2,4-thiadiazol-5-yl]oxy} -2,5-dimethylphenyl)-N-ethyl-N-methyl-imidoformamide,
(F338) N-(4-chlorobenzyl)-3-[3-methoxy-4-(prop-2-yn-l-yloxy)phenyl]propanamide, (F339) N-[(4- chlorophenyl)(cyano)methyl]-3-[3-methoxy-4-(prop-2-yn-l-yloxy)phenyl]propanamide, (F340) N-[(5- bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide, (F341) N-[l-(5-bromo-3- chloropyridin-2-yl)ethyl]-2,4-dichloropyridine-3-carboxamide, (F342) N-[l-(5-bromo-3-chloropyridin- 2-yl)ethyl]-2-fluoro-4-iodopyridine-3-carboxamide, (F343) N- {(E)-[(cyclopropylmethoxy)imino] [6- (difluoromethoxy)-2,3-difluoro-phenyl]methyl} -2-phenylacetamide (221201-92-9), (F344) N- {(Z)- [(cyclopropyl-methoxy)imino][6-(difluoromethoxy)-2,3-difluorophenyl]methyl}-2-phenylacet-amide (221201-92-9), (F345) N'- {4-[(3-tert-butyl-4-cyano-l,2-thiazol-5-yl)oxy]-2-chloro-5-methylphenyl}-N- ethyl-N-methylimidoformamide, (F346) N-methyl-2-(l- {[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl]acetyl}piperidin-4-yl)-N-(l ,2,3,4-tetrahydronaphthalen-l-yl)-l,3-thiazole-4-carboxamide (922514- 49-6), (F347) N-methyl-2-(l- {[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l-yl]acetyl}piperidin-4-yl)-N- [(lR)-l,2,3,4-tetrahydronaphthalen-l -yl]-l,3-thiazole-4-carboxamide (922514-07-6), (F348) N-methyl- 2-(l- {[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l -yl]acetyl}piperidin-4-yl)-N-[(lS)-l,2,3,4- tetrahydronaphthalen-l-yl]-l,3-thiazole-4-carboxamide (922514-48-5), (F349) pentyl {6-[({[(l-methyl- lH-tetrazol-5-yl)(phenyl)methylidene]amino}oxy)methyl]pyridin-2-yl}carbamate, (F350) phenazine-1- carboxylic acid, (F351) quinolin-8-ol (134-31-6), (F352) quinolin-8-ol sulfate (2: 1) (134-31 -6), (F353) tert-butyl {6- [( { [( 1 -methyl- 1 H-tetrazol-5-yl)(phenyl)methylene] amino } oxy)methyl]pyridin-2- yl} carbamate; - -
(16) Further compounds, like for example (F354) l-methyl-3-(trifluoromethyl)-N-[2'- (trifluoromethyl)biphenyl-2-yl]-lH-pyrazole-4-carboxamide, (F355) N-(4'-chlorobiphenyl-2-yl)-3- (difluoromethyl)- 1 -methyl- 1 H-pyrazole-4-carboxamide, (F356) N-(2',4'-dichlorobiphenyl-2-yl)-3 - (difluoromethyl)- 1 -methyl- 1 H-pyrazole-4-carboxamide, (F357) 3 -(difluoromethyl)- 1 -methyl-N- [4'- (trifluoromethyl)biphenyl-2-yl]-lH-pyrazole-4-carboxamide, (F358) N-(2',5'-difluorobiphenyl-2-yl)-l- methyl-3-(trifluoromethyl)-lH-pyrazole-4-carboxamide, (F359) 3 -(difluoromethyl)- 1 -methyl-N- [4'- (prop-l-yn-l-yl)biphenyl-2-yl]-lH-pyrazole-4-carboxamide, (F360) 5-fluoro-l,3-dimethyl-N-[4'-(prop- 1 -yn- 1 -yl)biphenyl-2-yl] - 1 H-pyrazole-4-carboxamide, (F361 ) 2-chloro-N- [4'-(prop- 1 -yn- 1 -yl)biphenyl- 2-yl]pyridine-3 -carboxamide, (F362) 3-(difluoromethyl)-N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2- yl]-l -methyl- lH-pyrazole-4-carboxamide, (F363) N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2-yl]-5- fluoro-l,3-dimethyl-lH-pyrazole-4-carboxamide, (F364) 3-(difluoromethyl)-N-(4'-ethynylbiphenyl-2- yl)-l -methyl- lH-pyrazole-4-carboxamide, (F365) N-(4'-ethynylbiphenyl-2-yl)-5-fluoro-l,3-dimethyl- lH-pyrazole-4-carboxamide, (F366) 2-chloro-N-(4'-ethynylbiphenyl-2-yl)pyridine-3-carboxamide, (F367) 2-chloro-N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2-yl]pyridine-3-carboxamide, (F368) 4- (difluoromethyl)-2-methyl-N-[4'-(trifluoromethyl)biphenyl-2-yl]-l,3-thiazole-5-carboxamide, (F369) 5- fluoro-N- [4'-(3 -hydroxy-3 -methylbut- 1 -yn- 1 -yl)biphenyl-2-yl] - 1 ,3 -dimethyl- 1 H-pyrazole-4- carboxamide, (F370) 2-chloro-N-[4'-(3-hydroxy-3-methylbut-l-yn-l-yl)biphenyl-2-yl]pyridine-3- carboxamide, (F371 ) 3 -(difluoro-methyl)-N- [4'-(3 -methoxy-3 -methylbut- 1 -yn- 1 -yl)biphenyl-2-yl] - 1 - methyl- lH-pyrazole-4-carboxamide, (F372) 5-fluoro-N-[4'-(3-methoxy-3-methylbut-l-yn-l- yl)biphenyl-2-yl]-l,3-dimethyl-lH-pyrazole-4-carboxamide, (F373) 2-chloro-N- [4'-(3 -methoxy-3 - methylbut- l-yn-l -yl)biphenyl-2-yl]pyridine-3 -carboxamide, (F374) (5-bromo-2-methoxy-4- methylpyridin-3-yl)(2,3,4-trimethoxy-6-methylphenyl)-methanone, (F375) N-[2-(4- {[3-(4- chlorophenyl)prop-2-yn-l-yl]oxy} -3-methoxy-phenyl)ethyl]-N2-(methylsulfonyl)valinamide (220706- 93-4), (F376) 4-oxo-4-[(2-phenylethyl)amino]butanoic acid, (F377) but-3-yn-l-yl {6-[({[(Z)-(l-methyl- lH-tetrazol-5-yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, (F378) 4-Amino-5- fluorpyrimidin-2-ol (mesomere Form: 6-Amino-5-fluorpyrimidin-2(lH)-on), (F379) propyl 3,4,5- trihydroxybenzoate and (F380) Oryzastrobin.
All named fungicides of the classes (1) to (16) (i. e. Fl to F380) can, if their functional groups enable this, optionally form salts with suitable bases or acids. In a preferred embodiment of the present invention the at least fungicide is a synthetic fungicide.
In one embodiment of the present invention the composition comprises two or more fungicides. In a preferred embodiment the composition comprises two or more of the above-mentioned preferred fungicides.
According to a preferred embodiment of the present invention the fungicide is selected from the group consisting of (1) Inhibitors of the ergosterol biosynthesis, for example (F3) bitertanol, (F4) - 5 - bromuconazole (116255-48-2), (F5) cyproconazole (1 13096-99-4), (F7) difenoconazole (119446-68-3), (F12) epoxiconazole (106325-08-0), (F16) fenhexamid (126833-17-8), (F17) fenpropidin (67306-00-7), (F18) fenpropimorph (67306-03-0), (F19) fluquinconazole (136426-54-5), (F22) flutriafol, (F26) imazalil, (F29) ipconazole (125225-28-7), (F30) metconazole (125116-23-6), (F31) myclobutanil (88671-89-0), (F37) penconazole (66246-88-6), (F39) prochloraz (67747-09-5), (F40) propiconazole (60207-90-1), (F41) prothioconazole (178928-70-6), (F44) quinconazole (103970-75-8), (F46) spiroxamine (118134-30-8), (F47) tebuconazole (107534-96-3), (F51) triadimenol (89482-17-7), (F55) triticonazole (131983-72-7);
(2) inhibitors of the respiratory chain at complex I or II, for example (F65) bixafen (581809-46-3), (F66) boscalid (188425-85-6), (F67) carboxin (5234-68-4), (F70) fluopyram (658066-35-4), (F71) flutolanil (66332-96-5), (F72) fluxapyroxad (907204-31-3), (F73) furametpyr (123572-88-3), (F75) isopyrazam (mixture of syn-epimeric racemate 1RS,4SR,9RS and anti-epimeric racemate 1RS,4SR,9SR) (881685- 58-1), (F76) isopyrazam (anti-epimeric racemate 1RS,4SR,9SR), (F77) isopyrazam (anti-epimeric enantiomer 1R,4S,9S), (F78) isopyrazam (anti-epimeric enantiomer 1 S,4R,9R), (F79) isopyrazam (syn epimeric racemate 1RS,4SR,9RS), (F80) isopyrazam (syn-epimeric enantiomer 1R,4S,9R), (F81) isopyrazam (syn-epimeric enantiomer 1 S,4R,9S), (F84) penflufen (494793-67-8), (F85) penthiopyrad (183675-82-3), (F86) sedaxane (874967-67-6), (F87) thifluzamide (130000-40-7), (F91) N-[l-(2,4- dichlorophenyl)- 1 -methoxypropan-2-yl] -3 -(difluoromethyl)- 1 -methyl- 1 H-pyrazole-4-carboxamide (1092400-95-7), (F98) l-Methyl-3-(trifluormethyl)-N-(l ,3,3-trimethyl-2,3-dihydro-lH-inden-4-yl)-lH- pyrazol-4-carboxamid, (F99) l-Methyl-3-(trifluormethyl)-N-[(l S)-l,3,3-trimethyl-2,3-dihydro-lH- inden-4-yl]-lH-pyrazol-4-carboxamid, (F100) l-Methyl-3-(trifluormethyl)-N-[(lR)-l,3,3-trimethyl-2,3- dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid, (F 101 ) 3 -(Difluormethyl)- 1 -methyl-N- [(3 S)- 1 , 1 ,3 - trimethyl-2,3 -dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid, (F 102) 3 -(Difluormethyl)- 1 -methyl-N- [(3R)- 1 , 1 ,3-trimethyl-2,3-dihydro- 1 H-inden-4-yl] - 1 H-pyrazol-4-carboxamid; (3) inhibitors of the respiratory chain at complex III, for example (F105) ametoctradin (865318-97-4), (F106) amisulbrom (348635-87-0), (F107) azoxystrobin (131860-33-8), (F108) cyazofamid (120116-88- 3), (Fi l l) dimoxystrobin (141600-52-4), (F112) enestroburin (238410-11-2), (F113) famoxadone (131807-57-3), (F114) fenamidone (161326-34-7), (F116) fluoxastrobin (361377-29-9), (F117) kresoxim-methyl (143390-89-0), (F118) metominostrobin (133408-50-1), (F119) orysastrobin (189892- 69-1), (F120) picoxystrobin (117428-22-5), (F121) pyraclostrobin (175013-18-0), (F124) pyribencarb (799247-52-2), (F126) trifloxystrobin (141517-21-7);
(4) Inhibitors of the mitosis and cell division, for example (F139) carbendazim (10605-21-7), (F140) chlorfenazole (3574-96-7), (F141) diethofencarb (87130-20-9), (F142) ethaboxam (162650-77-3), (F143) fluopicolide, (F144) fuberidazole (3878-19-1), (F145) pencycuron (66063-05-6), (F147) thiophanate-methyl (23564-05-8), (F149) zoxamide (156052-68-5); - -
(5) Compounds capable to have a multisite action, like for example (F154) captan (133-06-2), (F155) chlorothalonil (1897-45-6), (F156) copper hydroxide (20427-59-2), (F159) copper oxychloride (1332- 40-7), (F162) dithianon (3347-22-6), (F163) dodine (2439-10-3), (F167) folpet (133-07-3), (F168) guazatine (108173-90-6), (F172) iminoctadine triacetate (57520-17-9), (F174) mancozeb (8018-01-7), (F180) propineb (12071-83-9), (F 181 ) sulphur and sulphur preparations including calcium polysulphide (7704-34-9), (F182) thiram (137-26-8);
(6) Compounds capable to induce a host defence, like for example (F186) acibenzolar-S-methyl (135158-54-2),=(F187) isotianil (224049-04-1), (F189) tiadinil (223580-51-6);
(7) Inhibitors of the amino acid and/or protein biosynthesis, for example (F192) cyprodinil (121552-61- 2), (F196) pyrimethanil (53112-28-0);
(9) Inhibitors of the cell wall synthesis, for example (F202) benthiavalicarb (177406-68-7), (F203) dimethomorph (110488-70-5), (F205) iprovalicarb (140923-17-7), (F206) mandipropamid (374726-62- 2), (F210) valifenalate (283159-94-4; 283159-90-0);
(10) Inhibitors of the lipid and membrane synthesis, for example (F216) iodocarb (55406-53-6), (F217) iprobenfos (26087-47-8), (F220) propamocarb hydrochloride (25606-41-1), (F225) tolclofos-methyl;
11) Inhibitors of the melanine biosynthesis, for example (F226) carpropamid
(12) Inhibitors of the nucleic acid synthesis, for example (F233) benalaxyl (71626-11-4), (F234) benalaxyl-M (kiralaxyl) (98243-83-5), (F239) furalaxyl (57646-30-7), (F240) hymexazol (10004-44-1), (F241) metalaxyl (57837-19-1), (F242) metalaxyl-M (mefenoxam) (70630-17-0), (F244) oxadixyl (77732-09-3);
(13) Inhibitors of the signal transduction, for example (F247) fenpiclonil (74738-17-3), (F248) fludioxonil (131341-86-1), (F249) iprodione (36734-19-7), (F251) quinoxyfen (124495-18-7), (F252) vinclozolin (50471-44-8);
(14) Compounds capable to act as an uncoupler, like for example (F256) fluazinam (79622-59-6); (15) Further compounds, like for example (F266) cymoxanil (57966-95-7), (F280) flutianil (304900-25- 2), (F281) fosetyl-aluminium (39148-24-8), (F286) methasulfocarb (66952-49-6), (F287) methyl isothiocyanate (556-61-6), (F288) metrafenone (220899-03-6), (F298) phosphorous acid and its salts (13598-36-2), (F301) proquinazid (189278-12-4), (F309) triazoxide (72459-58-6) and (F319) 2,6- dimethyl-lH,5H-[l,4]dithiino[2,3-c:5,6-c']dipyrrole-l,3,5,7(2H,6H)-tetrone. In one embodiment of the present invention, the fungizide is selected from the group consisting of Carbendazim (F139), Carboxin (F67), Difenoconazole (F7), Fludioxonil (F248), Fluquinconazole (F19), - 7 -
Fluxapyroxad (F72), Ipconazole (F29), Isotianil (F187), Mefenoxam (F242), Metalaxyl (F241), Pencycuron (F145), Penflufen (F84), Prothioconazole (F41), Prochloraz (F39), Pyraclostrobin (F121), Sedaxane (F86), Silthiofam (F201), Tebuconazole (F47), Thiram (F182), Trifloxystrobin (F126), and Triticonazole (F55). Further additives
One aspect of the present invention is to provide a composition as described above additionally comprising at least one auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants. Those compositions are referred to as formulations.
Accordingly, in one aspect of the present invention such formulations, and application forms prepared from them, are provided as crop protection agents and/or pesticidal agents, such as drench, drip and spray liquors, comprising the composition of the invention. The application forms may comprise further crop protection agents and/or pesticidal agents, and/or activity- enhancing adjuvants such as penetrants, examples being vegetable oils such as, for example, rapeseed oil, sunflower oil, mineral oils such as, for example, liquid paraffins, alkyl esters of vegetable fatty acids, such as rapeseed oil or soybean oil methyl esters, or alkanol alkoxylates, and/or spreaders such as, for example, alkylsiloxanes and/or salts, examples being organic or inorganic ammonium or phosphonium salts, examples being ammonium sulphate or diammonium hydrogen phosphate, and/or retention promoters such as dioctyl sulphosuccinate or hydroxypropylguar polymers and/or humectants such as glycerol and/or fertilizers such as ammonium, potassium or phosphorous fertilizers, for example.
Examples of typical formulations include water-soluble liquids (SL), emulsifiable concentrates (EC), emulsions in water (EW), suspension concentrates (SC, SE, FS, OD), water-dispersible granules (WG), granules (GR) and capsule concentrates (CS); these and other possible types of formulation are described, for example, by Crop Life International and in Pesticide Specifications, Manual on development and use of FAO and WHO specifications for pesticides, FAO Plant Production and Protection Papers - 173, prepared by the FAO/WHO Joint Meeting on Pesticide Specifications, 2004, ISBN: 9251048576. The formulations may comprise active agrochemical compounds other than one or more active ingredients of the invention. The formulations or application forms in question preferably comprise auxiliaries, such as extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, biocides, thickeners and/or other auxiliaries, such as adjuvants, for example. An adjuvant in this context is a component which enhances the biological effect of the formulation, without the component itself having a biological effect. Examples of adjuvants are agents which promote the retention, spreading, attachment to the leaf surface, or penetration.
These formulations are produced in a known manner, for example by mixing the active ingredients with auxiliaries such as, for example, extenders, solvents and/or solid carriers and/or further auxiliaries, such as, for example, surfactants. The formulations are prepared either in suitable plants or else before or during the application.
Suitable for use as auxiliaries are substances which are suitable for imparting to the formulation of the active ingredient or the application forms prepared from these formulations (such as, e.g., usable crop protection agents, such as spray liquors or seed dressings) particular properties such as certain physical, technical and/or biological properties.
Suitable extenders are, for example, water, polar and nonpolar organic chemical liquids, for example from the classes of the aromatic and non-aromatic hydrocarbons (such as paraffins, alkylbenzenes, alkylnaphthalenes, chlorobenzenes), the alcohols and polyols (which, if appropriate, may also be substituted, etherified and/or esterified), the ketones (such as acetone, cyclohexanone), esters (including fats and oils) and (poly)ethers, the unsubstituted and substituted amines, amides, lactams (such as N- alkylpyrrolidones) and lactones, the sulphones and sulphoxides (such as dimethyl sulphoxide).
If the extender used is water, it is also possible to employ, for example, organic solvents as auxiliary solvents. Essentially, suitable liquid solvents are: aromatics such as xylene, toluene or alkylnaphthalenes, chlorinated aromatics and chlorinated aliphatic hydrocarbons such as chlorobenzenes, chloroethylenes or methylene chloride, aliphatic hydrocarbons such as cyclohexane or paraffins, for example petroleum fractions, mineral and vegetable oils, alcohols such as butanol or glycol and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, strongly polar solvents such as dimethylformamide and dimethyl sulphoxide, and also water. In principle it is possible to use all suitable solvents. Suitable solvents are, for example, aromatic hydrocarbons, such as xylene, toluene or alkylnaphthalenes, for example, chlorinated aromatic or aliphatic hydrocarbons, such as chlorobenzene, chloroethylene or methylene chloride, for example, aliphatic hydrocarbons, such as cyclohexane, for example, paraffins, petroleum fractions, mineral and vegetable oils, alcohols, such as methanol, ethanol, isopropanol, butanol or glycol, for example, and also their ethers and esters, ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone or cyclohexanone, for example, strongly polar solvents, such as dimethyl sulphoxide, and water.
All suitable carriers may in principle be used. Suitable carriers are in particular: for example, ammonium salts and ground natural minerals such as kaolins, clays, talc, chalk, quartz, attapulgite, montmorillonite or diatomaceous earth, and ground synthetic minerals, such as finely divided silica, alumina and natural or synthetic silicates, resins, waxes and/or solid fertilizers. Mixtures of such carriers may likewise be used. Carriers suitable for granules include the following: for example, crushed and fractionated natural minerals such as calcite, marble, pumice, sepiolite, dolomite, and also synthetic granules of inorganic and organic meals, and also granules of organic material such as sawdust, paper, coconut shells, maize cobs and tobacco stalks.
Liquefied gaseous extenders or solvents may also be used. Particularly suitable are those extenders or carriers which at standard temperature and under standard pressure are gaseous, examples being aerosol propellants, such as halogenated hydrocarbons, and also butane, propane, nitrogen and carbon dioxide.
Examples of emulsifiers and/or foam-formers, dispersants or wetting agents having ionic or nonionic properties, or mixtures of these surface-active substances, are salts of polyacrylic acid, salts of lignosulphonic acid, salts of phenolsulphonic acid or naphthalenesulphomc acid, polycondensates of ethylene oxide with fatty alcohols or with fatty acids or with fatty amines, with substituted phenols (preferably alkylphenols or arylphenols), salts of sulphosuccinic esters, taurine derivatives (preferably alkyltaurates), phosphoric esters of polyethoxylated alcohols or phenols, fatty acid esters of polyols, and derivatives of the compounds containing sulphates, sulphonates and phosphates, examples being alkylaryl polyglycol ethers, alkylsulphonates, alkyl sulphates, arylsulphonates, protein hydrolysates, lignin-sulphite waste liquors and methylcellulose. The presence of a surface-active substance is advantageous if one of the active ingredients and/or one of the inert carriers is not soluble in water and if application takes place in water. Further auxiliaries that may be present in the formulations and in the application forms derived from them include colorants such as inorganic pigments, examples being iron oxide, titanium oxide, Prussian Blue, and organic dyes, such as alizarin dyes, azo dyes and metal phthalocyanine dyes, and nutrients and trace nutrients, such as salts of iron, manganese, boron, copper, cobalt, molybdenum and zinc.
Stabilizers, such as low-temperature stabilizers, preservatives, antioxidants, light stabilizers or other agents which improve chemical and/or physical stability may also be present. Additionally present may be foam-formers or defoamers.
Furthermore, the formulations and application forms derived from them may also comprise, as additional auxiliaries, stickers such as carboxymethylcellulose, natural and synthetic polymers in powder, granule or latex form, such as gum arabic, polyvinyl alcohol, polyvinyl acetate, and also natural phospholipids, such as cephalins and lecithins, and synthetic phospholipids. Further possible auxiliaries include mineral and vegetable oils.
There may possibly be further auxiliaries present in the formulations and the application forms derived from them. Examples of such additives include fragrances, protective colloids, binders, adhesives, thickeners, thixotropic substances, penetrants, retention promoters, stabilizers, sequestrants, complexing - - agents, humectants and spreaders. Generally speaking, the active ingredients may be combined with any solid or liquid additive commonly used for formulation purposes.
Suitable retention promoters include all those substances which reduce the dynamic surface tension, such as dioctyl sulphosuccinate, or increase the viscoelasticity, such as hydroxypropylguar polymers, for example.
Suitable penetrants in the present context include all those substances which are typically used in order to enhance the penetration of active agrochemical compounds into plants. Penetrants in this context are defined in that, from the (generally aqueous) application liquor and/or from the spray coating, they are able to penetrate the cuticle of the plant and thereby increase the mobility of the active ingredients in the cuticle. This property can be determined using the method described in the literature (Baur et al., 1997, Pesticide Science 51, 131-152). Examples include alcohol alkoxylates such as coconut fatty ethoxylate (10) or isotridecyl ethoxylate (12), fatty acid esters such as rapeseed or soybean oil methyl esters, fatty amine alkoxylates such as tallowamine ethoxylate (15), or ammonium and/or phosphonium salts such as ammonium sulphate or diammonium hydrogen phosphate, for example. The formulations preferably comprise between 0.0001% and 98% by weight of active ingredients or, with particular preference, between 0.01% and 95% by weight of active ingredients, more preferably between 0.5% and 90% by weight of active ingredient, based on the weight of the formulation. The content of the active ingredients is defined as the sum of the pesticidal terpene mixture and the at least one insecticide and optionally the amount of fungicide. The pestcidial terpene mixture means the mixture of the three terpenes a-terpinene, p-cymene and limonene as essential components and optionally impurities such as those contained in the extract of Chenopodium ambrosioi des near ambrosioides. If, e.g. the commercial product Requiem® is used as pesticidal terpene mixture, the amount thereof is selected in such a way that the amount of the three pesticidal terpenes a-terpinene, p- cymene and limonene in total contained therein meets the requirements defined in the following. This definition applies throughout the following description as well.
The active ingredient content of the application forms (crop protection products) prepared from the formulations may vary within wide ranges. The active ingredient concentration of the application forms may be situated typically between 0.0001%> and 95% by weight of active ingredient, preferably between 0.001%) and 1%> by weight, based on the weight of the application form. Application takes place in a customary manner adapted to the application forms.
Furthermore, in one aspect of the present invention a kit of parts is provided comprising the pesticidal terpene mixture and at least one insecticide in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide are not identical, in a spatially separated arrangement. In a futher embodiment of the present invention the above-mentioned kit of parts further comprises at least one fungicide, with the proviso that the pesticidal terpene mixture and the fungicide are not identical. The fungicide can be present either in the pesticidal terpene mixture component of the kit of parts or in the insecticide component of the kit of parts being spatially separated or in both of these components. Preferably, the fungicide is present in the insecticide component.
Moreover, the kit of parts according to the present invention can additionally comprise at least one auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants as mentioned below. This at least one auxiliary can be present either in the pesticidal terpene mixture component of the kit of parts or in the insecticide component of the kit of parts being spatially separated or in both of these components.
In another aspect of the present invention the composition as described above is used for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, nematodes and/or phytopathogens.
Furthermore, in another aspect of the present invention the composition as described above increases the overall plant health.
The term "plant health" generally comprises various sorts of improvements of plants that are not connected to the control of pests. For example, advantageous properties that may be mentioned are improved crop characteristics including: emergence, crop yields, protein content, oil content, starch content, more developed root system, improved root growth, improved root size maintenance, improved root effectiveness, improved stress tolerance (e.g. against drought, heat, salt, UV, water, cold), reduced ethylene (reduced production and/or inhibition of reception), tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, pigment content, photosynthetic activity, less input needed (such as fertilizers or water), less seeds needed, more productive tillers, earlier flowering, early grain maturity, less plant verse (lodging), increased shoot growth, enhanced plant vigor, increased plant stand and early and better germination.
With regard to the use according to the present invention, improved plant health preferably refers to improved plant characteristics including: crop yield, more developed root system (improved root growth), improved root size maintenance, improved root effectiveness, tillering increase, increase in plant height, bigger leaf blade, less dead basal leaves, stronger tillers, greener leaf color, photosynthetic activity, more productive tillers, enhanced plant vigor, and increased plant stand.
With regard to the present invention, improved plant health preferably especially refers to improved plant properties selected from crop yield, more developed root system, improved root growth, improved root size maintenance, improved root effectiveness, tillering increase, and increase in plant height. The effect of a composition according to the present invention on plant health as defined herein can be determined by comparing plants which are grown under the same environmental conditions, whereby a part of said plants is treated with a composition according to the present invention and another part of said plants is not treated with a composition according to the present invention. Instead, said other part is not treated at all or treated with a placebo (i.e., an application without a composition according to the invention such as an application without all active ingredients (i.e. without a pesticidal terpene mixture as described herein and without an insecticide as described herein), or an application without a pesticidal terpene mixture as described herein, or an application without an insecticide as described herein.
The composition according to the present invention may be applied in any desired manner, such as in the form of a seed coating, soil drench, and/or directly in- furrow and/or as a foliar spray and applied either pre-emergence, post-emergence or both. In other words, the composition can be applied to the seed, the plant or to harvested fruits and vegetables or to the soil wherein the plant is growing or wherein it is desired to grow (plant's locus of growth).
Reducing the overall damage of plants and plant parts often results in healthier plants and/or in an increase in plant vigor and yield.
Preferably, the composition according to the present invention is used for treating conventional or transgenic plants or seed thereof.
Preferred plants and/or plant parts to be treated according to the invention are pepper {Capsicum annuum), cotton leaves (Gossypium hirsutum), bena plants (phaseolus vulgaris), Chinese cabbage (Brassica pekinensis), maize (Zeas mais) and French beans (Phaesolus vulgaris).
The composition of the invention has been proven to be particularly effective against infestation with green peach aphid (Myzus persicae), cotton aphid (Aphis gossypii), spotted spider mite (Tetranychus urticae), mustard beetle (Phaedon cochleriae), and fall armyworm (Spdoptera frugiperde).
In another aspect of the present invention a method for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, nematodes and/or phytopathogens is provided comprising the step of simultaneously or sequentially applying the pesticidal terpene mixture and at least one insecticide and optionally at least one fungicide on the plant, plant parts, harvested fruits, vegetables and/or plant's locus of growth in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the insecticide or fungicide are not identical. a preferred embodiment of the present method the at least one insecticide is a synthetic insecticide.
In another preferred embodiment of the present method the at least one fungicide is a synthetic fungicide. The method of the present invention includes the following application methods, namely both of the pesticidal terpene mixture and the at least one insecticide mentioned before may be formulated into a single, stable composition with an agriculturally acceptable shelf life (so called "solo-formulation"), or being combined before or at the time of use (so called "combined-formulations"). If not mentioned otherwise, the expression "combination" stands for the various combinations of the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide, in a solo-formulation, in a single "ready-mix" form, in a combined spray mixture composed from solo- formulations, such as a "tank-mix", and especially in a combined use of the single active ingredients when applied in a sequential manner, i.e. one after the other within a reasonably short period, such as a few hours or days, e.g. 2 hours to 7 days. The order of applying the composition according to the present invention is not essential for working the present invention. Accordingly, the term "combination" also encompasses the presence of the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide on or in a plant to be treated or its surrounding, habitat or storage space, e.g. after simultaneously or consecutively applying the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide to a plant its surrounding, habitat or storage space.
If the pectidial terpene mixture and the at least one insecticide, and optionally the at least one fungicide are employed or used in a sequential manner, it is preferred to treat the plants or plant parts (which includes seeds and plants emerging from the seed), harvested fruits and vegetables according to the following method: Firstly applying the at least one insecticide and optionally the at least one fungicide on the plant or plant parts, and secondly applying the pesticidal terpene mixture Jo the same plant or plant parts. The time periods between the first and the second application within a (crop) growing cycle may vary and depend on the effect to be achieved. For example, the first application is done to prevent an infestation of the plant or plant parts with insects, nematodes and/or phytopathogens (this is particularly the case when treating seeds) or to combat the infestation with insects, nematodes and/or phytopathogens (this is particularly the case when treating plants and plant parts) and the second application is done to prevent or control the infestation with insects, nematodes and/or phytopathogens. Control in this context means that the pesticidal terpene mixture is not able to fully exterminate the pests or phytopathogenic fungi but is able to keep the infestation on an acceptable level. The present invention also provides methods of enhancing the killing, inhibiting, preventative and/or repelling activity of the compositions of the present invention by multiple applications. In some other embodiments, the compositions of the present invention are applied to a plant and/or plant part for two times, during any desired development stages or under any predetermined pest pressure, at an interval of about 1 hour, about 5 hours, ab out 10 hours, about 24 hours, about two days, about 3 days, about 4 days, about 5 days, about 1 week, about 10 days, about two weeks, about three weeks, about 1 month or more. Still in some embodiments, the compositions of the present invention are applied to a plant and/or plant part for more than two times, for example, 3 times, 4 times, 5 times, 6 times, 7 times, 8 times, 9 times, 10 times, or more, during any desired development stages or under any predetermined pest pressure, at an interval of about 1 hour, about 5 hours, about 10 hours, about 24 hours, about two days, about 3 days, about 4 days, about 5 days, about lweek, about 10 days, about two weeks, about three weeks, about 1 month or more. The intervals between each application can vary if it is desired. One skilled in the artwill be able to determine the application times and length of interval depending on plant species, plant pest species, and other factors.
By following the before mentioned steps, a very low level of residues of the at least one insecticide, and optionally at least one fungicide on the treated plant, plant parts, and the harvested fruits and vegetables can be achieved.
If not mentioned otherwise the treatment of plants or plant parts (which includes seeds and plants emerging from the seed), harvested fruits and vegetables with the composition according to the invention is carried out directly or by action on their surroundings, habitat or storage space using customary treatment methods, for example dipping, spraying, atomizing, irrigating, evaporating, dusting, fogging, broadcasting, foaming, painting, spreading-on, watering (drenching), drip irrigating. It is furthermore possible to apply the at least one pesticidal terpene mixture, the at least one insecticide, and optionally the at least one fungicide as solo-formulation or combined-formulations by the ultra-low volume method, or to inject the composition according to the present invention as a composition or as sole-formulations into the soil (in-furrow). The term "plant to be treated" encompasses every part of a plant including its root system and the material - e.g., soil or nutrition medium - which is in a radius of at least 10 cm, 20 cm, 30 cm around the caulis or bole of a plant to be treated or which is at least 10 cm, 20 cm, 30 cm around the root system of said plant to be treated, respectively.
The amount of the pesticidal terpene mixture which is used or employed in combination with the at least one insecticide, optionally in the presence of a fungicide, depends on the final formulation as well as size or type of the plant, plant parts, seeds, harvested fruits and vegetables to be treated. Usually, the pesticidal terpene mixture to be employed or used according to the invention is present in about 2 % to about 80 % (w/w), preferably in about 5 % to about 75 % (w/w), more preferably about 10 % to about 70 % (w/w) of its solo-formulation or combined- formulation with the at least one insecticide, and optionally the fungicide.
Also the amount of the at least one insecticide which is used or employed in combination with the pesticidal terpene mixture, optionally in the presence of a fungicide, depends on the final formulation as well as size or type of the plant, plant parts, seeds, harvested fruit or vegetable to be treated. Usually, the insecticide to be employed or used according to the invention is present in about 0.1 % to about 80 % (w/w), preferably 1 % to about 60 % (w/w), more preferably about 10 % to about 50 % (w/w) of its 5 solo-formulation or combined- formulation with the pesticidal terpene mixture, and optionally the fungicide.
The pesticidal terpene mixture and at least one insecticide, and if present also the fungicide are used or employed in a synergistic weight ratio. The skilled person is able to find out the synergistic weight ratios for the present invention by routine methods. The skilled person understands that these ratios refer to the ratio within a combined-formulation as well as to the calculative ratio of the pesticidal terpene mixture described herein and the at least one insecticide when both components are applied as mono- formulations to a plant to be treated. The skilled person can calculate this ratio by simple mathematics since the volume and the amount of the pesticidal terpene mixture and insecticide, respectively, in a mono-formulation is known to the skilled person.
The ratio can be calculated based on the amount of the at least one insecticide, at the time point of applying said component of a combination according to the invention to a plant or plant part and the amount of the pesticidal terpene mixture shortly prior (e.g., 48 h, 24 h, 12 h, 6 h, 2 h, 1 h) or at the time point of applying said component of a combination according to the invention to a plant or plant part. The application of the pesticidal terpene mixture and the at least one insecticide to a plant or a plant part can take place simultaneously or at different times as long as both components are present on or in the plant after the application(s). In cases where the pesticidal terpene mixture and the insecticide are applied at different times and the insecticide is applied noticeable prior to the pesticidal terpene mixture, the skilled person can determine the concentration of the insecticide on/in a plant by chemical analysis known in the art, at the time point or shortly before the time point of applying the pesticidal terpene mixture. Vice versa, when the pesticidal terpene mixture is applied to a plant first, the concentration of the pesticidal terpene mixture can be determined using test which are also known in the art, at the time point or shortly before the time point of applying the insecticide.
In particular, in one embodiment the synergistic weight ratio of the pesticidal terpene mixture and the at least one insecticide lies in the range of 1 : 1000 to 1000 : 1, preferably in the range of 1 : 500 to 500 : 1, more preferably in the range of 1 : 500 to 300 : 1. For example, a ratio of 100: 1 means 100 weight parts of pesticidal terpene mixture and 1 weight part of the insecticide are combined (either as a solo formulation, a combined formulation or by separate applications to plants so that the combination is formed on the plant).
The application rate of composition to be employed or used according to the present invention may vary. The skilled person is able to find the appropriate application rate by way of routine experiments.
In another aspect of the present invention a seed treated with the composition as described above is provided.
The control of insects, nematodes and/or phytopathogens by treating the seed of plants has been known for a long time and is a subject of continual improvements. Nevertheless, the treatment of seed entails a - Jo - series of problems which cannot always be solved in a satisfactory manner. Thus, it is desirable to develop methods for protecting the seed and the germinating plant that remove the need for, or at least significantly reduce, the additional delivery of crop protection compositions in the course of storage, after sowing or after the emergence of the plants. It is desirable, furthermore, to optimize the amount of active ingredient employed in such a way as to provide the best-possible protection to the seed and the germinating plant from attack by insects, nematodes and/or phytopathogens, but without causing damage to the plant itself by the active ingredient employed. In particular, methods for treating seed ought also to take into consideration the intrinsic insecticidal and/or nematicidal properties of pest- resistant or pest-tolerant transgenic plants, in order to achieve optimum protection of the seed and of the germinating plant with a minimal use of crop protection compositions.
The present invention therefore also relates in particular to a method for protecting seed and germinating plants from attack by pests, by treating the seed with the pesticidal terpene mixture as defined above and at least one insecticide and optionally at least one fungicide of the invention. The method of the invention for protecting seed and germinating plants from attack by pests encompasses a method in which the seed is treated simultaneously in one operation with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide. It also encompasses a method in which the seed is treated at different times with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide.
The invention relates to the use of the composition of the invention for treating seed for the purpose of protecting the seed and the resultant plant against insects, mites, nematodes and/or phytopathogens.
The invention also relates to seed which at the same time has been treated with the pesticidal terpene mixture and at least one insecticide, and optionally at least one fungicide. The invention further relates to seed which has been treated at different times with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide. In the case of seed which has been treated at different times with the pesticidal terpene mixture and the at least one insecticide, and optionally the at least one fungicide, the individual active ingredients in the composition of the invention may be present in different layers on the seed.
Furthermore, the invention relates to seed which, following treatment with the composition of the invention, is subjected to a film-coating process in order to prevent dust abrasion of the seed. One of the advantages of the present invention is that, owing to the particular systemic properties of the compositions of the invention, the treatment of the seed with these compositions provides protection from insects, nematodes and/or phytopathogens not only to the seed itself but also to the plants originating from the seed, after they have emerged. In this way, it may not be necessary to treat the crop directly at the time of sowing or shortly thereafter. ?
A further advantage is to be seen in the fact that, through the treatment of the seed with composition of the invention, germination and emergence of the treated seed may be promoted.
It is likewise considered to be advantageous composition of the invention may also be used, in particular, on transgenic seed. It is also stated that the composition of the invention may be used in combination with agents of the signalling technology, as a result of which, for example, colonization with symbionts is improved, such as rhizobia, mycorrhiza and/or endophytic bacteria, for example, is enhanced, and/or nitrogen fixation is optimized.
The compositions of the invention are suitable for protecting seed of any variety of plant which is used in agriculture, in greenhouses, in forestry or in horticulture. More particularly, the seed in question is that of cereals (e.g. wheat, barley, rye, oats and millet), maize, cotton, soybeans, rice, potatoes, sunflower, coffee, tobacco, canola, oilseed rape, beets (e.g. sugar beet and fodder beet), peanuts, vegetables (e.g. tomato, cucumber, bean, brassicas, onions and lettuce), fruit plants, lawns and ornamentals. Particularly important is the treatment of the seed of cereals (such as wheat, barley, rye and oats) maize, soybeans, cotton, canola, oilseed rape and rice.
As already mentioned above, the treatment of transgenic seed with the composition of the invention is particularly important. The seed in question here is that of plants which generally contain at least one heterologous gene that controls the expression of a polypeptide having, in particular, insecticidal and/or nematicidal properties. These heterologous genes in transgenic seed may come from microorganisms such as Bacillus, Rhizobium, Pseudomonas, Serratia, Trichoderma, Clavibacter, Glomus or Gliocladium. The present invention is particularly suitable for the treatment of transgenic seed which contains at least one heterologous gene from Bacillus sp. With particular preference, the heterologous gene in question comes from Bacillus thuringiensis.
For the purposes of the present invention, the composition of the invention is applied alone or in a suitable formulation to the seed. The seed is preferably treated in a condition in which its stability is such that no damage occurs in the course of the treatment. Generally speaking, the seed may be treated at any point in time between harvesting and sowing. Typically, seed is used which has been separated from the plant and has had cobs, hulls, stems, husks, hair or pulp removed. Thus, for example, seed may be used that has been harvested, cleaned and dried to a moisture content of less than 15% by weight. Alternatively, seed can also be used that after drying has been treated with water, for example, and then dried again.
When treating seed it is necessary, generally speaking, to ensure that the amount of the composition of the invention, and/or of other additives, that is applied to the seed is selected such that the germination of the seed is not adversely affected, and/or that the plant which emerges from the seed is not damaged. This is the case in particular with active ingredients which may exhibit phytotoxic effects at certain application rates.
The compositions of the invention can be applied directly, in other words without comprising further components and without having been diluted. As a general rule, it is preferable to apply the compositions in the form of a suitable formulation to the seed. Suitable formulations and methods for seed treatment are known to the skilled person and are described in, for example, the following documents: US 4,272,417 A, US 4,245,432 A, US 4,808,430 A, US 5,876,739 A, US 2003/0176428 Al, WO 2002/080675 Al, WO 2002/028186 A2.
The combinations which can be used in accordance with the invention may be converted into the customary seed-dressing formulations, such as solutions, emulsions, suspensions, powders, foams, slurries or other coating compositions for seed, and also ULV formulations.
These formulations are prepared in a known manner, by mixing composition with customary adjuvants, such as, for example, customary extenders and also solvents or diluents, colorants, wetters, dispersants, emulsifiers, antifoams, preservatives, secondary thickeners, stickers, gibberellins, and also water. Colorants which may be present in the seed-dressing formulations which can be used in accordance with the invention include all colorants which are customary for such purposes. In this context it is possible to use not only pigments, which are of low solubility in water, but also water-soluble dyes. Examples include the colorants known under the designations Rhodamin B, C.I. Pigment Red 112 and C.I. Solvent Red 1. Wetters which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the substances which promote wetting and which are customary in the formulation of active agrochemical ingredients. Use may be made preferably of alkylnaphthalenesulphonates, such as diisopropyl- or diisobutyl-naphthalenesulphonates.
Dispersants and/or emulsifiers which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the nonionic, anionic and cationic dispersants that are customary in the formulation of active agrochemical ingredients. Use may be made preferably of nonionic or anionic dispersants or of mixtures of nonionic or anionic dispersants. Suitable nonionic dispersants are, in particular, ethylene oxide-propylene oxide block polymers, alkylphenol polyglycol ethers and also tristryrylphenol polyglycol ethers, and the phosphated or sulphated derivatives of these. Suitable anionic dispersants are, in particular, lignosulphonates, salts of polyacrylic acid, and arylsulphonate-formaldehyde condensates. Antifoams which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the foam inhibitors that are customary in the formulation of active agrochemical ingredients. Use may be made preferably of silicone antifoams and magnesium stearate.
Preservatives which may be present in the seed-dressing formulations which can be used in accordance with the invention include all of the substances which can be employed for such purposes in agrochemical compositions. Examples include dichlorophen and benzyl alcohol hemiformal.
Secondary thickeners which may be present in the seed-dressing formulations which can be used in accordance with the invention include all substances which can be used for such purposes in agrochemical compositions. Those contemplated with preference include cellulose derivatives, acrylic acid derivatives, xanthan, modified clays and highly disperse silica.
Stickers which may be present in the seed-dressing formulations which can be used in accordance with the invention include all customary binders which can be used in seed-dressing products. Preferred mention may be made of polyvinylpyrrolidone, polyvinyl acetate, polyvinyl alcohol and tylose.
Gibberellins which may be present in the seed-dressing formulations which can be used in accordance with the invention include preferably the gibberellins Al, A3 (= gibberellic acid), A4 and A7, with gibberellic acid being used with particular preference. The gibberellins are known (cf. R. Wegler, "Chemie der Pflanzenschutz- und Schadlingsbekampfungsmittel", Volume 2, Springer Verlag, 1970, pp. 401-412).
The seed-dressing formulations which can be used in accordance with the invention may be used, either directly or after prior dilution with water, to treat seed of any of a wide variety of types. Accordingly, the concentrates or the preparations obtainable from them by dilution with water may be employed to dress the seed of cereals, such as wheat, barley, rye, oats and triticale, and also the seed of maize, rice, oilseed rape, peas, beans, cotton, sunflowers and beets, or else the seed of any of a very wide variety of vegetables. The seed-dressing formulations which can be used in accordance with the invention, or their diluted preparations, may also be used to dress seed of transgenic plants. In that case, additional synergistic effects may occur in interaction with the substances formed through expression.
For the treatment of seed with the seed-dressing formulations which can be used in accordance with the invention, or with the preparations produced from them by addition of water, suitable mixing equipment includes all such equipment which can typically be employed for seed dressing. More particularly, the procedure when carrying out seed dressing is to place the seed in a mixer, to add the particular desired amount of seed-dressing formulations, either as such or following dilution with water beforehand, and to carry out mixing until the distribution of the formulation on the seed is uniform. This may be followed by a drying operation. The application rate of the seed-dressing formulations which can be used in accordance with the invention may be varied within a relatively wide range. It is guided by the particular amount of the at least one pesticidal terpene mixture and the at least one insecticide in the formulations, and by the seed. The application rates in the case of the composition are situated generally at between 0.001 and 50 g per kilogram of seed, preferably between 0.01 and 15 g per kilogram of seed.
The composition according to the invention, in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in protection of stored products and of materials, and in the hygiene sector. They can be preferably employed as plant protection agents. In particular, the present invention relates to the use of the composition according to the invention as insecticide and/or fungicide.
The composition according to the invention, in combination with good plant tolerance and favourable toxicity to warm-blooded animals and being tolerated well by the environment, are suitable for protecting plants and plant organs, for increasing harvest yields, for improving the quality of the harvested material and for controlling animal pests, in particular insects, arachnids, helminths, nematodes and molluscs, which are encountered in agriculture, in horticulture, in animal husbandry, in forests, in gardens and leisure facilities, in protection of stored products and of materials, and in the hygiene sector. They can be preferably employed as plant protection agents. In particular, the present invention relates to the use of the composition according to the invention as insecticide and/or fungicide.
The present composition preferably is active against normally sensitive and resistant species and against all or some stages of development. The abovementioned pests include: pests from the phylum Arthropoda, especially from the class Arachnida, for example, Acarus spp., Aceria sheldoni, Aculops spp., Aculus spp., Amblyomma spp., Amphitetranychus viennensis, Argas spp., Boophilus spp., Brevipalpus spp., Bryobia graminum, Bryobia praetiosa, Centruroides spp., Chorioptes spp., Dermanyssus gallinae, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Dermacentor spp., Eotetranychus spp., Epitrimerus pyri, Eutetranychus spp., Eriophyes spp., Glycyphagus domesticus, Halotydeus destructor, Hemitarsonemus spp., Hyalomma spp., Ixodes spp., Latrodectus spp., Loxosceles spp., Metatetranychus spp., Neutrombicula autumnalis, Nuphersa spp., Oligonychus spp., Ornithodorus spp., Ornithonyssus spp., Panonychus spp., Phyllocoptruta oleivora, Polyphagotarsonemus latus, Psoroptes spp., Rhipicephalus spp., Rhizoglyphus spp., Sarcoptes spp., Scorpio maurus, Steneotarsonemus spp., Steneotarsonemus spinki, Tarsonemus spp., Tetranychus spp., Trombicula alfreddugesi, Vaejovis spp., Vasates lycopersici; from the class Chilopoda, for example, Geophilus spp., Scutigera spp.; from the order or the class Collembola, for example, Onychiurus armatus; from the class Diplopoda, for example, Blaniulus guttulatus; from the class Insecta, e.g. from the order Blattodea, for example, Blattella asahinai, Blattella germanica, Blatta orientalis, Leucophaea maderae, Panchlora spp., Parcoblatta spp., Periplaneta spp., Supella longipalpa; from the order Coleoptera, for example, Acalymma vittatum, Acanthoscelides obtectus, Adoretus spp., Agelastica alni, Agriotes spp., Alphitobius diaperinus, Amphimallon solstitialis, Anobium punctatum, Anoplophora spp., Anthonomus spp., Anthrenus spp., Apion spp., Apogonia spp., Atomaria spp., Attagenus spp., Bruchidius obtectus, Bruchus spp., Cassida spp., Cerotoma trifurcata, Ceutorrhynchus spp., Chaetocnema spp., Cleonus mendicus, Conoderus spp., Cosmopolites spp., Costelytra zealandica, Ctenicera spp., Curculio spp., Cryptolestes ferrugineus, Cryptorhynchus lapathi, Cylindrocopturus spp., Dermestes spp., Diabrotica spp., Dichocrocis spp., Dicladispa armigera, Diloboderus spp., Epilachna spp., Epitrix spp., Faustinus spp., Gibbium psylloides, Gnathocerus cornutus, Hellula undalis, Heteronychus arator, Heteronyx spp., Hylamorpha elegans, Hylotrupes bajulus, Hypera postica, Hypomeces squamosus, Hypothenemus spp., Lachnosterna consanguinea, Lasioderma serricorne, Latheticus oryzae, Lathridius spp., Lema spp., Leptinotarsa decemlineata, Leucoptera spp., Lissorhoptrus oryzophilus, Lixus spp., Luperodes spp., Lyctus spp., Megascelis spp., Melanotus spp., Meligethes aeneus, Melolontha spp., Migdolus spp., Monochamus spp., Naupactus xanthographus, Necrobia spp., Niptus hololeucus, Oryctes rhinoceros, Oryzaephilus surinamensis, Oryzaphagus oryzae, Otiorrhynchus spp., Oxycetonia jucunda, Phaedon cochleariae, Phyllophaga spp., Phyllophaga helleri, Phyllotreta spp., Popillia japonica, Premnotrypes spp., Prostephanus truncatus, Psylliodes spp., Ptinus spp., Rhizobius ventralis, Rhizopertha dominica, Sitophilus spp., Sitophilus oryzae, Sphenophorus spp., Stegobium paniceum, Sternechus spp., Symphyletes spp., Tanymecus spp., Tenebrio molitor, Tenebrioides mauretanicus, Tribolium spp., Trogoderma spp., Tychius spp., Xylotrechus spp., Zabrus spp.; from the order Diptera, for example, Aedes spp., Agromyza spp., Anastrepha spp., Anopheles spp., Asphondylia spp., Bactrocera spp., Bibio hortulanus, Calliphora erythrocephala, Calliphora vicina, Ceratitis capitata, Chironomus spp., Chrysomyia spp., Chrysops spp., Chrysozona pluvialis, Cochliomyia spp., Contarinia spp., Cordylobia anthropophaga, Cricotopus sylvestris, Culex spp., Culicoides spp., Culiseta spp., Cuterebra spp., Dacus oleae, Dasyneura spp., Delia spp., Dermatobia hominis, Drosophila spp., Echinocnemus spp., Fannia spp., Gasterophilus spp., Glossina spp., Haematopota spp., Hydrellia spp., Hydrellia griseola, Hylemya spp., Hippobosca spp., Hypoderma spp., Liriomyza spp., Lucilia spp., Lutzomyia spp., Mansonia spp., Musca spp., Oestrus spp., Oscinella frit, - -
Paratanytarsus spp., Paralauterborniella subcincta, Pegomyia spp., Phlebotomus spp., Phorbia spp., Phormia spp., Piophila casei, Prodiplosis spp., Psila rosae, Rhagoletis spp., Sarcophaga spp., Simulium spp., Stomoxys spp., Tabanus spp., Tetanops spp., Tipula spp.; from the order Heteroptera, for example, Anasa tristis, Antestiopsis spp., Boisea spp., Blissus spp., Calocoris spp., Campylomma livida, Cavelerius spp., Cimex spp., Collaria spp., Creontiades dilutus, Dasynus piperis, Dichelops furcatus, Diconocoris hewetti, Dysdercus spp., Euschistus spp., Eurygaster spp., Heliopeltis spp., Horcias nobilellus, Leptocorisa spp., Leptocorisa varicornis, Leptoglossus phyllopus, Lygus spp., Macropes excavatus, Miridae, Monalonion atratum, Nezara spp., Oebalus spp., Pentomidae, Piesma quadrata, Piezodorus spp., Psallus spp., Pseudacysta persea, Rhodnius spp., Sahlbergella singularis, Scaptocoris castanea, Scotinophora spp., Stephanitis nashi, Tibraca spp., Triatoma spp.; from the order Homoptera, for example, Acizzia acaciaebaileyanae, Acizzia dodonaeae, Acizzia uncatoides, Acrida turrita, Acyrthosipon spp., Acrogonia spp., Aeneolamia spp., Agonoscena spp., Aleyrodes proletella, Aleurolobus barodensis, Aleurothrixus floccosus, Allocaridara malayensis, Amrasca spp., Anuraphis cardui, Aonidiella spp., Aphanostigma piri, Aphis spp., Arboridia apicalis, Arytainilla spp., Aspidiella spp., Aspidiotus spp., Atanus spp., Aulacorthum solani, Bemisia tabaci, Blastopsylla occidentalis, Boreioglycaspis melaleucae, Brachycaudus helichrysi, Brachycolus spp., Brevicoryne brassicae, Cacopsylla spp., Calligypona marginata, Cameocephala fulgida, Ceratovacuna lanigera, Cercopidae, Ceroplastes spp., Chaetosiphon fragaefolii, Chionaspis tegalensis, Chlorita onukii, Chondracris rosea, Chromaphis juglandicola, Chrysomphalus ficus, Cicadulina mbila, Coccomytilus halli, Coccus spp., Cryptomyzus ribis, Cryptoneossa spp., Ctenarytaina spp., Dalbulus spp., Dialeurodes citri, Diaphorina citri, Diaspis spp., Drosicha spp., Dysaphis spp., Dysmicoccus spp., Empoasca spp., Eriosoma spp., Erythroneura spp., Eucalyptolyma spp., Euphyllura spp., Euscelis bilobatus, Ferrisia spp., Geococcus coffeae, Glycaspis spp., Heteropsylla cubana, Heteropsylla spinulosa, Homalodisca coagulata, Hyalopterus arundinis, Icerya spp., Idiocerus spp., Idioscopus spp., Laodelphax striatellus, Lecanium spp., Lepidosaphes spp., Lipaphis erysimi, Macrosiphum spp., Macrosteles facifrons, Mahanarva spp., Melanaphis sacchari, Metcalfiella spp., Metopolophium dirhodum, Monellia costalis, Monelliopsis pecanis, Myzus spp., Nasonovia ribisnigri, Nephotettix spp., Nettigoniclla spectra, Nilaparvata lugens, Oncometopia spp., Orthezia praelonga, Oxya chinensis, Pachypsylla spp., Parabemisia myricae, Paratrioza spp., Parlatoria spp., Pemphigus spp., Peregrinus maidis, Phenacoccus spp., Phloeomyzus passerinii, Phorodon humuli, Phylloxera spp., Pinnaspis aspidistrae, Planococcus spp., Prosopidopsylla flava, Protopulvinaria pyriformis, Pseudaulacaspis pentagona, Pseudococcus spp., Psyllopsis spp., Psylla spp., Pteromalus spp., Pyrilla spp., Quadraspidiotus spp., Quesada gigas, Rastrococcus spp., Rhopalosiphum spp., Saissetia spp., Scaphoideus titanus, Schizaphis graminum, Selenaspidus articulatus, Sogata spp., Sogatella furcifera, Sogatodes spp., Stictocephala festina, Siphoninus phillyreae, Tenalaphara malayensis, Tetragonocephela spp., Tinocallis caryaefoliae, Tomaspis spp., Toxoptera spp., Trialeurodes vaporariorum, Trioza spp., Typhlocyba spp., Unaspis spp., Viteus vitifolii, Zygina spp.; from the order Hymenoptera, for example, Acromyrmex spp., Athalia spp., Atta spp., Diprion spp., Hoplocampa spp., Lasius spp., Monomorium pharaonis, Sirex spp., Solenopsis invicta, Tapinoma spp., Urocerus spp., Vespa spp., Xeris spp.; from the order Isopoda, for example, Armadillidium vulgare, Oniscus asellus, Porcellio scaber; from the order Isoptera, for example, Coptotermes spp., Cornitermes cumulans, Cryptotermes spp., Incisitermes spp., Microtermes obesi, Odontotermes spp., Reticulitermes spp.; from the order Lepidoptera, for example, Achroia grisella, Acronicta major, Adoxophyes spp., Aedia leucomelas, Agrotis spp., Alabama spp., Amyelois transitella, Anarsia spp., Anticarsia spp., Argyroploce spp., Barathra brassicae, Borbo cinnara, Bucculatrix thurberiella, Bupalus piniarius, Busseola spp., Cacoecia spp., Caloptilia theivora, Capua reticulana, Carpocapsa pomonella, Carposina niponensis, Cheimatobia brumata, Chilo spp., Choristoneura spp., Clysia ambiguella, Cnaphalocerus spp., Cnaphalocrocis medinalis, Cnephasia spp., Conopomorpha spp., Conotrachelus spp., Copitarsia spp., Cydia spp., Dalaca noctuides, Diaphania spp., Diatraea saccharalis, Earias spp., Ecdytolopha aurantium, Elasmopalpus lignosellus, Eldana saccharina, Ephestia spp., Epinotia spp., Epiphyas postvittana, Etiella spp., Eulia spp., Eupoecilia ambiguella, Euproctis spp., Euxoa spp., Feltia spp., Galleria mellonella, Gracillaria spp., Grapholitha spp., Hedylepta spp., Helicoverpa spp., Heliothis spp., Hofmannophila pseudospretella, Homoeosoma spp., Homona spp., Hyponomeuta padella, Kakivoria flavofasciata, Laphygma spp., Laspeyresia molesta, Leucinodes orbonalis, Leucoptera spp., Lithocolletis spp., Lithophane antennata, Lobesia spp., Loxagrotis albicosta, Lymantria spp., Lyonetia spp., Malacosoma neustria, Maruca testulalis, Mamstra brassicae, Melanitis leda, Mocis spp., Monopis obviella, Mythimna separata, Nemapogon cloacellus, Nymphula spp., Oiketicus spp., Oria spp., Orthaga spp., Ostrinia spp., Oulema oryzae, Panolis flammea, Parnara spp., Pectinophora spp., Perileucoptera spp., Phthorimaea spp., Phyllocnistis citrella, Phyllonorycter spp., Pieris spp., Platynota stultana, Plodia interpunctella, Plusia spp., Plutella xylostella, Prays spp., Prodenia spp., Protoparce spp., Pseudaletia spp., Pseudaletia unipuncta, Pseudoplusia includens, Pyrausta nubilalis, Rachiplusia nu, Schoenobius spp., Scirpophaga spp., Scirpophaga innotata, Scotia segetum, Sesamia spp., Sesamia inferens, Sparganothis spp., Spodoptera spp., Spodoptera praefica, Stathmopoda spp., Stomopteryx subsecivella, Synanthedon spp., Tecia solanivora, Thermesia gemmatalis, Tinea cloacella, Tinea pellionella, Tineola bisselliella, Tortrix spp., Trichophaga tapetzella, Trichoplusia spp., Tryporyza incertulas, Tuta absoluta, Virachola spp.; from the order Orthoptera or Saltatoria, for example, Acheta domesticus, Dichroplus spp., Gryllotalpa spp., Hieroglyphus spp., Locusta spp., Melanoplus spp., Schistocerca gregaria; from the order Phthiraptera, for example, Damalinia spp., Haematopinus spp., Linognathus spp., Pediculus spp., Ptirus pubis, Trichodectes spp.; from the order Psocoptera for example Lepinatus spp., Liposcelis spp.; from the order Siphonaptera, for example, Ceratophyllus spp., Ctenocephalides spp., Pulex irritans, Tunga penetrans, Xenopsylla cheopsis; from the order Thysanoptera, for example, Anaphothrips obscurus, Baliothrips biformis, Drepanothrips reuteri, Enneothrips flavens, Frankliniella spp., Heliothrips spp., Hercinothrips femoralis, Rhipiphorothrips cruentatus, Scirtothrips spp., Taeniothrips cardamomi, Thrips spp.; from the order Zygentoma (=Thysanura), for example, Ctenolepisma spp., Lepisma saccharina, Lepismodes inquilinus, Thermobia domestica; from the class Symphyla, for example, Scutigerella spp.; pests from the phylum Mollusca, especially from the class Bivalvia, for example, Dreissena spp., and from the class Gastropoda, for example, Arion spp., Biomphalaria spp., Bulinus spp., Deroceras spp., Galba spp., Lymnaea spp., Oncomelania spp., Pomacea spp., Succinea spp.; animal pests from the phylums Plathelminthes and Nematoda, for example, Ancylostoma duodenale, Ancylostoma ceylanicum, Acylostoma braziliensis, Ancylostoma spp., Ascaris spp., Brugia malayi, Brugia timori, Bunostomum spp., Chabertia spp., Clonorchis spp., Cooperia spp., Dicrocoelium spp., Dictyocaulus filaria, Diphyllobothrium latum, Dracunculus medinensis, Echinococcus granulosus, Echinococcus multilocularis, Enterobius vermicularis, Faciola spp., Haemonchus spp., Heterakis spp., Hymenolepis nana, Hyostrongulus spp., Loa Loa, Nematodirus spp., Oesophagostomum spp., Opisthorchis spp., Onchocerca volvulus, Ostertagia spp., Paragonimus spp., Schistosomen spp., Strongyloides fuelleborni, Strongyloides stercoralis, Stronyloides spp., Taenia saginata, Taenia solium, Trichinella spiralis, Trichinella nativa, Trichinella britovi, Trichinella nelsoni, Trichinella pseudopsiralis, Trichostrongulus spp., Trichuris trichuria, Wuchereria bancrofti; phytoparasitic pests from the phylum Nematoda, for example, Aphelenchoides spp., Bursaphelenchus spp., Ditylenchus spp., Globodera spp., Heterodera spp., Longidorus spp., Meloidogyne spp., Pratylenchus spp., Radopholus spp., Trichodorus spp., Tylenchulus spp., Xiphinema spp., Helicotylenchus spp., Tylenchorhynchus spp., Scutellonema spp., Paratrichodorus spp., Meloinema spp., Paraphelenchus spp., Aglenchus spp., Belonolaimus spp., Nacobbus spp., Rotylenchulus spp., Rotylenchus spp., Neotylenchus spp., Paraphelenchus spp., Dolichodorus spp., Hoplolaimus spp., Punctodera spp., Criconemella spp., Quinisulcius spp., Hemicycliophora spp., Anguina spp., Subanguina 5 spp., Hemicriconemoides spp., Psilenchus spp., Pseudohalenchus spp., Criconemoides spp., Cacopaurus spp., Hirschmaniella spp, Tetylenchus spp.,
It is furthermore possible to control organisms from the subphylum Protozoa, especially from the order Coccidia, such as Eimeria spp. Furthermore, in case the pesticidal terpene mixture exhibits fungicidal activity and/or the composition additionally comprises a fungicide, the composition according to the present invention has potent microbicidal activity and can be used for control of unwanted microorganisms, such as fungi and bacteria, in crop protection and in the protection of materials.
The invention also relates to a method for controlling unwanted microorganisms, characterized in that the inventive composition is applied to the phytopathogenic fungi, phytopathogenic bacteria and/or their habitat.
Fungicides can be used in crop protection for control of phytopathogenic fungi. They are characterized by an outstanding efficacy against a broad spectrum of phytopathogenic fungi, including soilborne pathogens, which are in particular members of the classes Plasmodiophoromycetes , Peronosporomycetes (Syn. Oomycetes), Chytridiomycetes , Zygomycetes, Ascomycetes, Basidiomycetes and Deuteromycetes (Syn. Fungi imperfecti). Some fungicides are systemically active and can be used in plant protection as foliar, seed dressing or soil fungicide. Furthermore, they are suitable for combating fungi, which inter alia infest wood or roots of plant.
Bactericides can be used in crop protection for control of Pseudomonadaceae, Rhizobiaceae, Enterobacteriaceae, Corynebacteriaceae and Streptomycetaceae.
Non-limiting examples of pathogens of fungal diseases which can be treated in accordance with the invention include: diseases caused by powdery mildew pathogens, for example Blumeria species, for example Blumeria graminis; Podosphaera species, for example Podosphaera leucotricha; Sphaerotheca species, for example Sphaerotheca fuliginea; Uncinula species, for example Uncinula necator; diseases caused by rust disease pathogens, for example Gymnosporangium species, for example Gymnosporangium sabinae; Hemileia species, for example Hemileia vastatrix; Phakopsora species, for example Phakopsora pachyrhizi and Phakopsora meibomiae; Puccinia species, for example Puccinia recondite, P. triticina, P. graminis or P. striiformis; Uromyces species, for example Uromyces appendiculatus; diseases caused by pathogens from the group of the Oomycetes, for example Albugo species, for example Algubo Candida; Bremia species, for example Bremia lactucae; Peronospora species, for - - example Peronospora pisi or P. brassicae; Phytophthora species, for example Phytophthora infestans; Plasmopara species, for example Plasmopara viticola; Pseudoperonospora species, for example Pseudoperonospora humuli or Pseudoperonospora cubensis; Pythium species, for example Pythium ultimum; leaf blotch diseases and leaf wilt diseases caused, for example, by Alternaria species, for example Alternaria solani; Cercospora species, for example Cercospora beticola; Cladiosporium species, for example Cladiosporium cucumerinum; Cochliobolus species, for example Cochliobolus sativus (conidia form: Drechslera, Syn: Helminthosporium), Cochliobolus miyabeanus; Colletotrichum species, for example Colletotrichum lindemuthanium; Cycloconium species, for example Cycloconium oleaginum; Diaporthe species, for example Diaporthe citri; Elsinoe species, for example Elsinoe fawcettii; Gloeosporium species, for example Gloeosporium laeticolor; Glomerella species, for example Glomerella cingulata; Guignardia species, for example Guignardia bidwelli; Leptosphaeria species, for example Leptosphaeria maculans, Leptosphaeria nodorum; Magnaporthe species, for example Magnaporthe grisea; Microdochium species, for example Microdochium nivale; Mycosphaerella species, for example Mycosphaerella graminicola, M. arachidicola and M. fijiensis; Phaeosphaeria species, for example Phaeosphaeria nodorum; Pyrenophora species, for example Pyrenophora teres, Pyrenophora tritici repentis; Ramularia species, for example Ramularia collo-cygni, Ramularia areola; Rhynchosporium species, for example Rhynchosporium secalis; Septoria species, for example Septoria apii, Septoria lycopersii; Typhula species, for example Typhula incarnata; Venturia species, for example Venturia inaequalis; root and stem diseases caused, for example, by Corticium species, for example Corticium graminearum; Fusarium species, for example Fusarium oxysporum; Gaeumannomyces species, for example Gaeumannomyces graminis; Rhizoctonia species, such as, for example Rhizoctonia solani; Sarodadium diseases caused for example by Sarodadium oryzae; Sclerotium diseases caused for example by Sclerotium oryzae; Tapesia species, for example Tapesia acuformis; Thielaviopsis species, for example Thielaviopsis basicola; ear and panicle diseases (including corn cobs) caused, for example, by Alternaria species, for example Alternaria spp.; Aspergillus species, for example Aspergillus flavus; Cladosporium species, for example Cladosporium cladosporioides; Claviceps species, for example Claviceps purpurea; Fusarium species, for example Fusarium culmorum; Gibberella species, for example Gibberella zeae; Monographella species, for example Monographella nivalis; Septoria species, for example Septoria nodorum; diseases caused by smut fungi, for example Sphacelotheca species, for example Sphacelotheca reiliana; Tilletia species, for example Tilletia caries, T. controversa; Urocystis species, for example Urocystis occulta; Ustilago species, for example Ustilago nuda, U. nuda tritici; - 7 - fruit rot caused, for example, by Aspergillus species, for example Aspergillus flavus; Botrytis species, for example Botrytis cinerea; Penicillium species, for example Penicillium expansum and P. purpurogenum; Sclerotinia species, for example Sclerotinia sderotiorum; Verticilium species, for example Verticilium alboatrum; seed and soilborne decay, mould, wilt, rot and damping-off diseases caused, for example, by Alternaria species, caused for example by Alternaria brassicicola; Aphanomyces species, caused for example by Aphanomyces euteiches; Ascochyta species, caused for example by Ascochyta lentis; Aspergillus species, caused for example by Aspergillus flavus; Cladosporium species, caused for example by Cladosporium herbarum; Cochliobolus species, caused for example by Cochliobolus sativus; (Conidiaform: Drechslera, Bipolaris Syn: Helminthosporium); Colletotrichum species, caused for example by Colletotrichum coccodes; Fusarium species, caused for example by Fusarium culmorum; Gibberella species, caused for example by Gibberella zeae; Macrophomina species, caused for example by Macrophomina phaseolina; Monographella species, caused for example by Monographella nivalis; Penicillium species, caused for example by Penicillium expansum; Phoma species, caused for example by Phoma lingam; Phomopsis species, caused for example by Phomopsis sojae; Phytophthora species, caused for example by Phytophthora cactorum; Pyrenophora species, caused for example by Pyrenophora graminea; Pyricularia species, caused for example by Pyricularia oryzae; Pythium species, caused for example by Pythium ultimum; Rhizoctonia species, caused for example by Rhizoctonia solani; Rhizopus species, caused for example by Rhizopus oryzae; Sclerotium species, caused for example by Sclerotium rolfsii; Septoria species, caused for example by Septoria nodorum; Typhula species, caused for example by Typhula incarnata; Verticillium species, caused for example by Verticillium dahliae; cancers, galls and witches' broom caused, for example, by Nectria species, for example Nectria galligena; wilt diseases caused, for example, by Monilinia species, for example Monilinia laxa; leaf blister or leaf curl diseases caused, for example, by Exobasidium species, for example Exobasidium vexans;
Taphrina species, for example Taphrina deformans; decline diseases of wooden plants caused, for example, by Esca disease, caused for example by Phaemoniella clamydospora, Phaeoacremonium aleophilum and Fomitiporia mediterranea; Eutypa dyeback, caused for example by Eutypa lata ; Ganoderma diseases caused for example by Ganoderma boninense; Rigidoporus diseases caused for example by Rigidoporus lignosus; diseases of flowers and seeds caused, for example, by Botrytis species, for example Botrytis cinerea; - - diseases of plant tubers caused, for example, by Rhizoctonia species, for example Rhizoctonia solani; Helminthosporium species, for example Helminthosporium solani;
Club root caused, for example, by Plasmodiophora species, for example Plamodiophora brassicae; diseases caused by bacterial pathogens, for example Xanthomonas species, for example Xanthomonas campestris pv. oryzae; Pseudomonas species, for example Pseudomonas syringae pv. lachrymans; Erwinia species, for example Erwinia amylovora.
The following diseases of soya beans can be controlled with preference:
Fungal diseases on leaves, stems, pods and seeds caused, for example, by Alternaria leaf spot (Alternaria spec, atrans tenuissima), Anthracnose (Colletotrichum gloeosporoides dematium var. truncatum), brown spot (Septoria glycines), cercospora leaf spot and blight (Cercospora kikuchii), choanephora leaf blight (Choanephora infundibulifera trispora (Syn.)), dactuliophora leaf spot (Dactuliophora glycines), downy mildew (Peronospora manshurica), drechslera blight (Drechslera glycini), frogeye leaf spot (Cercospora sojina), leptosphaerulina leaf spot (LeptosphaeruUna trifolu), phyllostica leaf spot (Phyllosticta sojaecola), pod and stem blight (Phomopsis sojae), powdery mildew (Microsphaera diffusa), pyrenochaeta leaf spot (Pyrenochaeta glycines), rhizoctonia aerial, foliage, and web blight (Rhizoctonia solani), rust (Phakopsora pachyrhizi, Phakopsora meibomiae), scab (Sphaceloma glycines), stemphylium leaf blight (Stemphylium botryosum), target spot (Corynespora cassiicola).
Fungal diseases on roots and the stem base caused, for example, by black root rot (Calonectria crotalariae), charcoal rot (Macrophomina phaseolina), fusarium blight or wilt, root rot, and pod and collar rot (Fusarium oxysporum, Fusarium orthoceras, Fusarium semitectum, Fusarium equiseti), mycoleptodiscus root rot (Mycoleptodiscus terrestris), neocosmospora (Neocosmospora vasinfecta), pod and stem blight (Diaporthe phaseolorum), stem canker (Diaporthe phaseolorum var. caulivora), phytophthora rot (Phytophthora megasperma), brown stem rot (Phialophora gregata), pythium rot (Pythium aphanidermatum, Pythium irregulare, Pythium debaryanum, Pythium myriotylum, Pythium ultimum), rhizoctonia root rot, stem decay, and damping-off (Rhizoctonia solani), sclerotinia stem decay (Sclerotinia sclerotiorum), sclerotinia southern blight (Sclerotinia rolfsii), thielaviopsis root rot (Thielaviopsis basicola).
The inventive compositions can be used for curative or protective/preventive control of phytopathogenic fungi. The invention therefore also relates to curative and protective methods for controlling phytopathogenic fungi by the use of the inventive composition, which is applied to the seed, the plant or plant parts, the fruit or the soil in which the plants grow. The fact that the composition is well tolerated by plants at the concentrations required for controlling plant diseases allows the treatment of above-ground parts of plants, of propagation stock and seeds, and of the soil.
According to the invention all plants and plant parts can be treated. By plants is meant all plants and plant populations such as desirable and undesirable wild plants, cultivars and plant varieties (whether or not protectable by plant variety or plant breeder's rights). Cultivars and plant varieties can be plants obtained by conventional propagation and breeding methods which can be assisted or supplemented by one or more biotechnological methods such as by use of double haploids, protoplast fusion, random and directed mutagenesis, molecular or genetic markers or by bioengineering and genetic engineering methods. By plant parts is meant all above ground and below ground parts and organs of plants such as shoot, leaf, blossom and root, whereby for example leaves, needles, stems, branches, blossoms, fruiting bodies, fruits and seed as well as roots, corms and rhizomes are listed. Crops and vegetative and generative propagating material, for example cuttings, corms, rhizomes, runners and seeds also belong to plant parts. The inventive composition, when it is well tolerated by plants, has favourable homeotherm toxicity and is well tolerated by the environment, is suitable for protecting plants and plant organs, for enhancing harvest yields, for improving the quality of the harvested material. It can preferably be used as crop protection composition. It is active against normally sensitive and resistant species and against all or some stages of development. Plants which can be treated in accordance with the invention include the following main crop plants: maize, soya bean, alfalfa, cotton, sunflower, Brassica oil seeds such as Brassica napus (e.g. canola, rapeseed), Brassica rapa, B. juncea (e.g. (field) mustard) and Brassica carinata, Arecaceae sp. (e.g. oilpalm, coconut), rice, wheat, sugar beet, sugar cane, oats, rye, barley, millet and sorghum, triticale, flax, nuts, grapes and vine and various fruit and vegetables from various botanic taxa, e.g. Rosaceae sp. (e.g. pome fruits such as apples and pears, but also stone fruits such as apricots, cherries, almonds, plums and peaches, and berry fruits such as strawberries, raspberries, red and black currant and gooseberry), Ribesioidae sp., Juglandaceae sp., Betulaceae sp., Anacardiaceae sp., Fagaceae sp., Moraceae sp., Oleaceae sp. (e.g. olive tree), Actinidaceae sp., Lauraceae sp. (e.g. avocado, cinnamon, camphor), Musaceae sp. (e.g. banana trees and plantations), Rubiaceae sp. (e.g. coffee), Theaceae sp. (e.g. tea), Sterculiceae sp., Rutaceae sp. (e.g. lemons, oranges, mandarins and grapefruit); Solanaceae sp. (e.g. tomatoes, potatoes, peppers, capsicum, aubergines, tobacco), Liliaceae sp., Compositae sp. (e.g. lettuce, artichokes and chicory - including root chicory, endive or common chicory), Umbelliferae sp. (e.g. carrots, parsley, celery and celeriac), Cucurbitaceae sp. (e.g. cucumbers - including gherkins, pumpkins, watermelons, calabashes and melons), AUiaceae sp. (e.g. leeks and onions), Cruciferae sp. (e.g. white cabbage, red cabbage, broccoli, cauliflower, Brussels sprouts, pak choi, kohlrabi, radishes, horseradish, cress and Chinese cabbage), Leguminosae sp. (e.g. peanuts, peas, lentils and beans - e.g. 5 common beans and broad beans), Chenopodiaceae sp. (e.g. Swiss chard, fodder beet, spinach, beetroot), Linaceae sp. (e.g. hemp), Cannabeacea sp. (e.g. cannabis), Malvaceae sp. (e.g. okra, cocoa), Papaveraceae (e.g. poppy), Asparagaceae (e.g. asparagus); useful plants and ornamental plants in the garden and woods including turf, lawn, grass and Stevia rebaudiana; and in each case genetically modified types of these plants.
Depending on the plant species or plant cultivars, their location and growth conditions (soils, climate, vegetation period, diet), using or employing the composition according to the present invention the treatment according to the invention may also result in super-additive ("synergistic") effects. Thus, for example, by using or employing inventive composition in the treatment according to the invention, reduced application rates and/or a widening of the activity spectrum and/or an increase in the activity better plant growth, increased tolerance to high or low temperatures, increased tolerance to drought or to water or soil salt content, increased flowering performance, easier harvesting, accelerated maturation, higher harvest yields, bigger fruits, larger plant height, greener leaf color, earlier flowering, higher quality and/or a higher nutritional value of the harvested products, higher sugar concentration within the fruits, better storage stability and/or processability of the harvested products are possible, which exceed the effects which were actually to be expected.
At certain application rates of the inventive composition in the treatment according to the invention may also have a strengthening effect in plants. The defense system of the plant against attack by unwanted phytopathogenic fungi and/ or microorganisms and/or viruses is mobilized. Plant-strengthening (resistance-inducing) substances are to be understood as meaning, in the present context, those substances or combinations of substances which are capable of stimulating the defense system of plants in such a way that, when subsequently inoculated with unwanted phytopathogenic fungi and/or microorganisms and/or viruses, the treated plants display a substantial degree of resistance to these phytopathogenic fungi and/or microorganisms and/or viruses, Thus, by using or employing composition according to the present invention in the treatment according to the invention, plants can be protected against attack by the abovementioned pathogens within a certain period of time after the treatment. The period of time within which protection is effected generally extends from 1 to 10 days, preferably 1 to 7 days, after the treatment of the plants with the active ingredients.
Plants and plant cultivars which are also preferably to be treated according to the invention are resistant against one or more biotic stresses, i.e. said plants show a better defense against animal and microbial pests, such as against nematodes, insects, mites, phytopathogenic fungi, bacteria, viruses and/or viroids.
Plants and plant cultivars which may also be treated according to the invention are those plants which are resistant to one or more abiotic stresses, i. e. that already exhibit an increased plant health with respect to stress tolerance. Abiotic stress conditions may include, for example, drought, cold temperature exposure, heat exposure, osmotic stress, flooding, increased soil salinity, increased mineral exposure, ozon exposure, high light exposure, limited availability of nitrogen nutrients, limited availability of 5 phosphorus nutrients, shade avoidance. Preferably, the treatment of these plants and cultivars with the composition of the present invention additionally increases the overall plant health (cf. above).
Plants and plant cultivars which may also be treated according to the invention, are those plants characterized by enhanced yield characteristics i. e. that already exhibit an increased plant health with respect to this feature. Increased yield in said plants can be the result of, for example, improved plant physiology, growth and development, such as water use efficiency, water retention efficiency, improved nitrogen use, enhanced carbon assimilation, improved photosynthesis, increased germination efficiency and accelerated maturation. Yield can furthermore be affected by improved plant architecture (under stress and non-stress conditions), including but not limited to, early flowering, flowering control for hybrid seed production, seedling vigor, plant size, internode number and distance, root growth, seed size, fruit size, pod size, pod or ear number, seed number per pod or ear, seed mass, enhanced seed filling, reduced seed dispersal, reduced pod dehiscence and lodging resistance. Further yield traits include seed composition, such as carbohydrate content, protein content, oil content and composition, nutritional value, reduction in anti-nutritional compounds, improved processability and better storage stability. Preferably, the treatment of these plants and cultivars with the composition of the present invention additionally increases the overall plant health (cf. above).
Plants that may be treated according to the invention are hybrid plants that already express the characteristic of heterosis or hybrid vigor which results in generally higher yield, vigor, health and resistance towards biotic and abiotic stress factors. Such plants are typically made by crossing an inbred male-sterile parent line (the female parent) with another inbred male-fertile parent line (the male parent). Hybrid seed is typically harvested from the male sterile plants and sold to growers. Male sterile plants can sometimes (e.g. in corn) be produced by detasseling, i.e. the mechanical removal of the male reproductive organs (or males flowers) but, more typically, male sterility is the result of genetic determinants in the plant genome. In that case, and especially when seed is the desired product to be harvested from the hybrid plants it is typically useful to ensure that male fertility in the hybrid plants is fully restored. This can be accomplished by ensuring that the male parents have appropriate fertility restorer genes which are capable of restoring the male fertility in hybrid plants that contain the genetic determinants responsible for male-sterility. Genetic determinants for male sterility may be located in the cytoplasm. Examples of cytoplasmic male sterility (CMS) were for instance described in Brassica species. However, genetic determinants for male sterility can also be located in the nuclear genome. Male sterile plants can also be obtained by plant biotechnology methods such as genetic engineering. A particularly useful means of obtaining male-sterile plants is described in WO 89/10396 in which, for example, a ribonuclease such as barnase is selectively expressed in the tapetum cells in the stamens. Fertility can then be restored by expression in the tapetum cells of a ribonuclease inhibitor such as barstar.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may be treated according to the invention are herbicide-tolerant plants, i.e. plants made tolerant to one or 5 more given herbicides. Such plants can be obtained either by genetic transformation, or by selection of plants containing a mutation imparting such herbicide tolerance.
Herbicide-tolerant plants are for example glyphosate-tolerant plants, i.e. plants made tolerant to the herbicide glyphosate or salts thereof. Plants can be made tolerant to glyphosate through different means. For example, glyphosate-tolerant plants can be obtained by transforming the plant with a gene encoding the enzyme 5-enolpyruvylshikimate-3-phosphate synthase (EPSPS). Examples of such EPSPS genes are the AroA gene (mutant CT7) of the bacterium Salmonella typhimurium, the CP4 gene of the bacterium Agrobacterium sp, the genes encoding a Petunia EPSPS, a Tomato EPSPS, or an Eleusine EPSPS. It can also be a mutated EPSPS. Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate oxido-reductase enzyme. Glyphosate-tolerant plants can also be obtained by expressing a gene that encodes a glyphosate acetyl transferase enzyme. Glyphosate-tolerant plants can also be obtained by selecting plants containing naturally- occurring mutations of the above-mentioned genes.
Other herbicide resistant plants are for example plants that are made tolerant to herbicides inhibiting the enzyme glutamine synthase, such as bialaphos, phosphinothricin or glufosinate. Such plants can be obtained by expressing an enzyme detoxifying the herbicide or a mutant glutamine synthase enzyme that is resistant to inhibition. One such efficient detoxifying enzyme is an enzyme encoding a phosphinothricin acetyltransferase (such as the bar or pat protein from Streptomyces species). Plants expressing an exogenous phosphinothricin acetyltransferase are also described.
Further herbicide-tolerant plants are also plants that are made tolerant to the herbicides inhibiting the enzyme hydroxyphenylpyruvatedioxygenase (HPPD). Hydroxyphenylpyruvatedioxygenases are enzymes that catalyze the reaction in which para-hydroxyphenylpyruvate (HPP) is transformed into homogentisate. Plants tolerant to HPPD-inhibitors can be transformed with a gene encoding a naturally- occurring resistant HPPD enzyme, or a gene encoding a mutated HPPD enzyme. Tolerance to HPPD- inhibitors can also be obtained by transforming plants with genes encoding certain enzymes enabling the formation of homogentisate despite the inhibition of the native HPPD enzyme by the HPPD-inhibitor. Tolerance of plants to HPPD inhibitors can also be improved by transforming plants with a gene encoding an enzyme prephenate dehydrogenase in addition to a gene encoding an HPPD-tolerant enzyme.
Still further herbicide resistant plants are plants that are made tolerant to aceto lactate synthase (ALS) inhibitors. Known ALS-inhibitors include, for example, sulfonylurea, imidazolinone, triazolopyrimidines, pyrimidinyoxy(thio)benzoates, and/or sulfonylaminocarbonyltriazolinone herbicides. Different mutations in the ALS enzyme (also known as acetohydroxyacid synthase, AHAS) are known to confer tolerance to different herbicides and groups of herbicides. The production of sulfonylurea-tolerant plants and imidazolinone-tolerant plants is described in WO 1996/033270. Other 5 imidazolinone-tolerant plants are also described. Further sulfonylurea- and imidazolinone-tolerant plants are also described in for example WO 2007/024782.
Other plants tolerant to imidazolinone and/or sulfonylurea can be obtained by induced mutagenesis, selection in cell cultures in the presence of the herbicide or mutation breeding as described for example for soybeans, for rice, for sugar beet, for lettuce, or for sunflower.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are insect-resistant transgenic plants, i.e. plants made resistant to attack by certain target insects. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such insect resistance.
An "insect-resistant transgenic plant", as used herein, includes any plant containing at least one transgene comprising a coding sequence encoding:
1) An insecticidal crystal protein from Bacillus thuringiensis or an insecticidal portion thereof, such as the insecticidal crystal proteins listed online at:
http://www.lifesci.sussex.ac.uk/Home/Neil_Crickmore/Bt/, or insecticidal portions thereof, e.g., proteins of the Cry protein classes CrylAb, CrylAc, CrylF, Cry2Ab, Cry3Aa, or Cry3Bb or insecticidal portions thereof; or
2) a crystal protein from Bacillus thuringiensis or a portion thereof which is insecticidal in the presence of a second other crystal protein from Bacillus thuringiensis or a portion thereof, such as the binary toxin made up of the Cry34 and Cry35 crystal proteins; or
3) a hybrid insecticidal protein comprising parts of different insecticidal crystal proteins from Bacillus thuringiensis, such as a hybrid of the proteins of 1) above or a hybrid of the proteins of 2) above, e.g., the CrylA.105 protein produced by corn event MON98034 (WO 2007/027777); or
4) a protein of any one of 1) to 3) above wherein some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation, such as the Cry3Bbl protein in corn events MON863 or MON88017, or the Cry3A protein in corn event MIR604;
5) an insecticidal secreted protein from Bacillus thuringiensis or Bacillus cereus, or an insecticidal portion thereof, such as the vegetative insecticidal (VIP) proteins listed at:
http://www.lifesci.sussex.ac.uk/home/Neil_Crickmore/Bt/vip.html, e.g. proteins from the VIP3Aa protein class; or
6) secreted protein from Bacillus thuringiensis or Bacillus cereus which is insecticidal in the presence of a second secreted protein from Bacillus thuringiensis or B. cereus, such as the binary toxin made up of the VIP1 A and VIP2A proteins; or 5
7) hybrid insecticidal protein comprising parts from different secreted proteins from Bacillus thuringiensis or Bacillus cereus, such as a hybrid of the proteins in 1) above or a hybrid of the proteins in 2) above; or
8) protein of any one of 1) to 3) above wherein some, particularly 1 to 10, amino acids have been replaced by another amino acid to obtain a higher insecticidal activity to a target insect species, and/or to expand the range of target insect species affected, and/or because of changes introduced into the encoding DNA during cloning or transformation (while still encoding an insecticidal protein), such as the VIP3Aa protein in cotton event COT 102.
Of course, an insect-resistant transgenic plant, as used herein, also includes any plant comprising a combination of genes encoding the proteins of any one of the above classes 1 to 8. In one embodiment, an insect-resistant plant contains more than one transgene encoding a protein of any one of the above classes 1 to 8, to expand the range of target insect species affected when using different proteins directed at different target insect species, or to delay insect resistance development to the plants by using different proteins insecticidal to the same target insect species but having a different mode of action, such as binding to different receptor binding sites in the insect.
Plants or plant cultivars which may also be treated according to the invention are nematode resistant plants. Examples of nematode resistant plants are described in e.g. US Patent Application Nos 11/765,491, 11/765,494, 10/926,819, 10/782,020, 12/032,479, 10/783,417, 10/782,096, 11/657,964, 12/192,904, 11/396,808, 12/166,253, 12/166,239, 12/166,124, 12/166,209, 11/762,886, 12/364,335, 11/763,947, 12/252,453, 12/209,354, 12/491,396 or 12/497,221.
Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are tolerant to abiotic stresses. Such plants can be obtained by genetic transformation, or by selection of plants containing a mutation imparting such stress resistance. Particularly useful stress tolerance plants include:
a. plants which contain a transgene capable of reducing the expression and/or the activity of poly(ADP-ribose)polymerase (PARP) gene in the plant cells or plants
b. plants which contain a stress tolerance enhancing transgene capable of reducing the expression and/or the activity of the poly(ADP-ribose)glycohydrolase (PARG) encoding genes of the plants or plants cells.
c. plants which contain a stress tolerance enhancing transgene coding for a plant-functional enzyme of the nicotinamide adenine dinucleotide salvage synthesis pathway including nicotinamidase, nicotinate phosphoribosyltransferase, nicotinic acid mononucleotide adenyl transferase, nicotinamide adenine dinucleotide synthetase or nicotine amide phosphorybosyltransferase. Plants or plant cultivars (obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention show altered quantity, quality and/or storage-stability of the harvested product and/or altered properties of specific ingredients of the harvested product such as :
1) transgenic plants which synthesize a modified starch, which in its physical-chemical characteristics, in particular the amylose content or the amylose/amylopectin ratio, the degree of branching, the average chain length, the side chain distribution, the viscosity behaviour, the gelling strength, the starch grain size and/or the starch grain morphology, is changed in comparison with the synthesised starch in wild type plant cells or plants, so that this is better suited for special applications.
2) transgenic plants which synthesize non starch carbohydrate polymers or which synthesize non starch carbohydrate polymers with altered properties in comparison to wild type plants without genetic modification. Examples are plants producing polyfructose, especially of the inulin and levan-type, plants producing alpha 1,4 glucans, plants producing alpha- 1,6 branched alpha- 1,4- glucans, plants producing alternan,
3) transgenic plants which produce hyaluronan.
Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as cotton plants, with altered fiber characteristics. Such plants can be obtained by genetic transformation or by selection of plants contain a mutation imparting such altered fiber characteristics and include:
a) Plants, such as cotton plants, containing an altered form of cellulose synthase genes, b) Plants, such as cotton plants, containing an altered form of rsw2 or rsw3 homologous nucleic acids,
c) Plants, such as cotton plants, with increased expression of sucrose phosphate synthase, d) Plants, such as cotton plants, with increased expression of sucrose synthase,
e) Plants, such as cotton plants, wherein the timing of the plasmodesmatal gating at the basis of the fiber cell is altered, e.g. through downregulation of fiberselective β 1,3-glucanase,
f) Plants, such as cotton plants, having fibers with altered reactivity, e.g. through the expression of N-acteylglucosaminetransferase gene including nodC and chitinsynthase genes.
Plants or plant cultivars (that can be obtained by plant biotechnology methods such as genetic engineering) which may also be treated according to the invention are plants, such as oilseed rape or related Brassica plants, with altered oil profile characteristics. Such plants can be obtained by genetic transformation or by selection of plants contain a mutation imparting such altered oil characteristics and include:
a) Plants, such as oilseed rape plants, producing oil having a high oleic acid content,
b) Plants such as oilseed rape plants, producing oil having a low linolenic acid content, c) Plant such as oilseed rape plants, producing oil having a low level of saturated fatty acids. Particularly useful transgenic plants which may be treated according to the invention are plants which comprise one or more genes which encode one or more toxins, such as the following which are sold under the trade names YIELD GARD® (for example maize, cotton, soya beans), KnockOut® (for example maize), BiteGard® (for example maize), Bt-Xtra® (for example maize), StarLink® (for example maize), Bollgard® (cotton), Nucotn® (cotton), Nucotn 33B® (cotton), NatureGard® (for example maize), Protecta® and NewLeaf® (potato). Examples of herbicide-tolerant plants which may be mentioned are maize varieties, cotton varieties and soya bean varieties which are sold under the trade names Roundup Ready® (tolerance to glyphosate, for example maize, cotton, soya bean), Liberty Link® (tolerance to phosphinotricin, for example oilseed rape), IMI® (tolerance to imidazolinones) and STS® (tolerance to sulphonylureas, for example maize). Herbicide-resistant plants (plants bred in a conventional manner for herbicide tolerance) which may be mentioned include the varieties sold under the name Clearfield® (for example maize).
Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or a combination of transformation events, and that are listed for example in the databases for various national or regional regulatory agencies including Event 1143-14A (cotton, insect control, not deposited, described in WO 06/128569); Event 1143-51B (cotton, insect control, not deposited, described in WO 06/128570); Event 1445 (cotton, herbicide tolerance, not deposited, described in US-A 2002-120964 or WO 02/034946); Event 17053 (rice, herbicide tolerance, deposited as PTA-9843, described in WO 10/117737); Event 17314 (rice, herbicide tolerance, deposited as PTA-9844, described in WO 10/117735); Event 281-24-236 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in WO 05/103266 or US-A 2005-216969); Event 3006- 210-23 (cotton, insect control - herbicide tolerance, deposited as PTA-6233, described in US-A 2007- 143876 or WO 05/103266); Event 3272 (corn, quality trait, deposited as PTA-9972, described in WO 06/098952 or US-A 2006-230473); Event 40416 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-11508, described in WO 11/075593); Event 43A47 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-11509, described in WO 11/075595); Event 5307 (corn, insect control, deposited as ATCC PTA-9561, described in WO 10/077816); Event ASR-368 (bent grass, herbicide tolerance, deposited as ATCC PTA-4816, described in US-A 2006-162007 or WO 04/053062); Event B16 (corn, herbicide tolerance, not deposited, described in US-A 2003-126634); Event BPS-CV127-9 (soybean, herbicide tolerance, deposited as NCIMB No. 41603, described in WO 10/080829); Event CE43-67B (cotton, insect control, deposited as DSM ACC2724, described in US-A 2009-217423 or WO 06/128573); Event CE44-69D (cotton, insect control, not deposited, described in US-A 2010-0024077); Event CE44-69D (cotton, insect control, not deposited, described in WO 06/128571); Event CE46-02A (cotton, insect control, not deposited, described in WO 06/128572); Event COT102 (cotton, insect control, not deposited, described in US-A 2006-130175 or WO 04/039986); Event COT202 (cotton, insect control, not deposited, described in US-A 2007-067868 or WO 05/054479); Event COT203 (cotton, insect control, not deposited, described in WO 05/054480); Event 5?
DAS40278 (corn, herbicide tolerance, deposited as ATCC PTA-10244, described in WO 11/022469); Event DAS-59122-7 (corn, insect control - herbicide tolerance, deposited as ATCC PTA 11384 , described in US-A 2006-070139); Event DAS-59132 (corn, insect control - herbicide tolerance, not deposited, described in WO 09/100188); Event DAS68416 (soybean, herbicide tolerance, deposited as ATCC PTA-10442, described in WO 11/066384 or WO 11/066360); Event DP-098140-6 (corn, herbicide tolerance, deposited as ATCC PTA-8296, described in US-A 2009-137395 or WO 08/112019); Event DP-305423-1 (soybean, quality trait, not deposited, described in US-A 2008-312082 or WO 08/054747); Event DP-32138-1 (corn, hybridization system, deposited as ATCC PTA-9158, described in US-A 2009-0210970 or WO 09/103049); Event DP-356043-5 (soybean, herbicide tolerance, deposited as ATCC PTA-8287, described in US-A 2010-0184079 or WO 08/002872); Event EE-1 (brinjal, insect control, not deposited, described in WO 07/091277); Event FI117 (corn, herbicide tolerance, deposited as ATCC 209031, described in US-A 2006-059581 or WO 98/044140); Event GA21 (corn, herbicide tolerance, deposited as ATCC 209033, described in US-A 2005-086719 or WO 98/044140); Event GG25 (corn, herbicide tolerance, deposited as ATCC 209032, described in US-A 2005-188434 or WO 98/044140); Event GHB119 (cotton, insect control - herbicide tolerance, deposited as ATCC PTA-8398, described in WO 08/151780); Event GHB614 (cotton, herbicide tolerance, deposited as ATCC PTA-6878, described in US-A 2010-050282 or WO 07/017186); Event GJ11 (corn, herbicide tolerance, deposited as ATCC 209030, described in US-A 2005-188434 or WO 98/044140); Event GM RZ13 (sugar beet, virus resistance , deposited as NCIMB-41601, described in WO 10/076212); Event H7-1 (sugar beet, herbicide tolerance, deposited as NCIMB 41158 or NCIMB 41159, described in US-A 2004-172669 or WO 04/074492); Event JOPLIN1 (wheat, disease tolerance, not deposited, described in US-A 2008-064032); Event LL27 (soybean, herbicide tolerance, deposited as NCIMB41658, described in WO 06/108674 or US-A 2008-320616); Event LL55 (soybean, herbicide tolerance, deposited as NCIMB 41660, described in WO 06/108675 or US-A 2008-196127); Event LLcotton25 (cotton, herbicide tolerance, deposited as ATCC PTA-3343, described in WO 03/013224 or US-A 2003-097687); Event LLRICE06 (rice, herbicide tolerance, deposited as ATCC-23352, described in US 6,468,747 or WO 00/026345); Event LLRICE601 (rice, herbicide tolerance, deposited as ATCC PTA-2600, described in US-A 2008-2289060 or WO 00/026356); Event LY038 (corn, quality trait, deposited as ATCC PTA-5623, described in US-A 2007-028322 or WO 05/061720); Event MIR162 (corn, insect control, deposited as PTA-8166, described in US-A 2009-300784 or WO 07/142840); Event MIR604 (corn, insect control, not deposited, described in US-A 2008-167456 or WO 05/103301); Event MON15985 (cotton, insect control, deposited as ATCC PTA-2516, described in US-A 2004- 250317 or WO 02/100163); Event MON810 (corn, insect control, not deposited, described in US-A 2002-102582); Event MON863 (corn, insect control, deposited as ATCC PTA-2605, described in WO 04/011601 or US-A 2006-095986); Event MON87427 (corn, pollination control, deposited as ATCC PTA-7899, described in WO 11/062904); Event MON87460 (corn, stress tolerance, deposited as ATCC PTA-8910, described in WO 09/111263 or US-A 2011-0138504); Event MON87701 (soybean, insect control, deposited as ATCC PTA-8194, described in US-A 2009-130071 or WO 09/064652); Event 5
MON87705 (soybean, quality trait - herbicide tolerance, deposited as ATCC PTA-9241, described in US-A 2010-0080887 or WO 10/037016); Event MON87708 (soybean, herbicide tolerance, deposited as ATCC PTA9670, described in WO 11/034704); Event MON87754 (soybean, quality trait, deposited as ATCC PTA-9385, described in WO 10/024976); Event MON87769 (soybean, quality trait, deposited as ATCC PTA-8911, described in US-A 2011-0067141 or WO 09/102873); Event MON88017 (corn, insect control - herbicide tolerance, deposited as ATCC PTA-5582, described in US-A 2008-028482 or WO 05/059103); Event MON88913 (cotton, herbicide tolerance, deposited as ATCC PTA-4854, described in WO 04/072235 or US-A 2006-059590); Event MON89034 (corn, insect control, deposited as ATCC PTA-7455, described in WO 07/140256 or US-A 2008-260932); Event MON89788 (soybean, herbicide tolerance, deposited as ATCC PTA-6708, described in US-A 2006-282915 or WO 06/130436); Event MS 11 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-850 or PTA-2485, described in WO 01/031042); Event MS8 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01/041558 or US-A 2003-188347); Event NK603 (corn, herbicide tolerance, deposited as ATCC PTA-2478, described in US-A 2007- 292854); Event PE-7 (rice, insect control, not deposited, described in WO 08/114282); Event RF3 (oilseed rape, pollination control - herbicide tolerance, deposited as ATCC PTA-730, described in WO 01/041558 or US-A 2003-188347); Event RT73 (oilseed rape, herbicide tolerance, not deposited, described in WO 02/036831 or US-A 2008-070260); Event T227-1 (sugar beet, herbicide tolerance, not deposited, described in WO 02/44407 or US-A 2009-265817); Event T25 (corn, herbicide tolerance, not deposited, described in US-A 2001-029014 or WO 01/051654); Event T304-40 (cotton, insect control - herbicide tolerance, deposited as ATCC PTA-8171, described in US-A 2010-077501 or WO 08/122406); Event T342-142 (cotton, insect control, not deposited, described in WO 06/128568); Event TC1507 (corn, insect control - herbicide tolerance, not deposited, described in US-A 2005-039226 or WO 04/099447); Event VIP 1034 (corn, insect control - herbicide tolerance, deposited as ATCC PTA- 3925., described in WO 03/052073), Event 32316 (corn, insect control-herbicide tolerance, deposited as PTA-11507, described in WO 11/084632), Event 4114 (corn, insect control-herbicide tolerance, deposited as PTA-11506, described in WO 11/084621).
Particularly useful transgenic plants which may be treated according to the invention are plants containing transformation events, or combination of transformation events, that are listed for example in the databases from various national or regional regulatory agencies (see for example http://gmoinfo.jrc.it/gmp_browse.aspx and http://www.agbios.com/dbase.php).
Examples
Example A - 5 -
Myzus persicae - spray test
Solvent: 7 parts by weight of dimethylformamide
Emulsifier: 2 parts by weight of alkylaryl polyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration, if necessary.
Pepper leaves {Capsicum annuum) which are heavily infested by the green peach aphid {Myzus persicae) are treated by being sprayed with the preparation of the active compound of the desired concentration.
After the specified period of time, mortality in % is determined. 100 % means all the aphids have been killed; 0 % means none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table A-l : Myzus persicae - test
Active Ingredient Concentration Efficacy
in ppm in % after 4d
Requiem (QRD 4.052) 2000 5
Clothianidin (I142) 0.5 65
0.25 10
0.125 3
Requiem + Clothianidin) obs.* cal.**
(4000 : 1) 2000 + 0.5 94 66.75
(8000 : 1) 2000 + 0.25 93 14.5
(16000 : 1) 2000 + 0.125 55 7.85
according to the invention
Table A-2: Myzus persicae - test
Active Ingredient Concentration Efficacy
in ppm in % after 5d - -
Figure imgf000061_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example B
Aphis gossypii - spray test
Solvent: 7 parts by weight of dimethylformamide
Emulsifier: 2 parts by weight of alkylaryl polyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration, if necessary.
Cotton leaves (Gossypium hirsutum) which are heavily infested by the cotton aphid {Aphis gossypii) are treated by being sprayed with the preparation of the active compound of the desired concentration. After the specified period of time, the mortality in % is determined. 100 % means all the aphids have been killed; 0 % means none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table B: Aphis gossypii - test - -
Active Ingredient Concentration Efficacy
in ppm in % after Id
Requiem (QRD 4.052) 3000 10
2000 0
BCS-CL73507 1 10
Requiem + BCS-CL73507 obs.* cal.**
(3000 : 1) 3000 + 1 50 19
according to the invention
Chlorantraniliprole (1231) 8 50
4 10
Requiem + Chlorantraniliprole
(3000 : 1) obs.* cal.**
(6000 : 1) 3000 + 8 80 55
according to the invention 3000 + 4 55 19
Clothianidin (I142) 0.5 8
0.25 3
Requiem + Clothianidin obs.* cal.**
(4000 : 1) 2000 + 0.5 80 8
(8000 : 1) 2000 + 0.25 55 3
according to the invention
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example C
Tetranychus urticae - spray test, OP-resistant
Solvent: 7 parts by weight of dimethylformamide
Emulsifier: 2 parts by weight of alkylaryl polyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration if necessary.
Bean plants (Phaseolus vulgaris) which are heavily infested with all stages of the two-spotted spider mite (Tetranychus urticae) are treated by being sprayed with the preparation of the active compound of the desired concentration. After the specified period of time, mortality in % is determined. 100 % means all the spider mites have been killed; 0 % means none of the spider mites have been killed. The mortality values determined thus are recalculated using the Colby-formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table C: Tetranychus urticae
Figure imgf000063_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula Example D
Phaedon cochleariae - spray test
Solvent: 78.0 parts by weight of acetone
1.5 parts by weight of dimethylformamide
Emulsifier: 0.5 parts by weight of alkylaryl polyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration.
Chinese cabbage (Brassica pekinensis) leaf- disks are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf disks are infested with mustard beetle larvae {Phaedon cochleariae). After the specified period of time, mortality in % is determined. 100 % means all beetle larvae have been killed and 0 % means none of the beetle larvae have been killed. The mortality values determined thus are recalculated using the Colby-formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table D: Phaedon cochleariae - test
Figure imgf000064_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example E
Spodoptera frugiperda - spray test
Solvent: 78.0 parts by weight acetone
1.5 parts by weight dimethylformamide
Emulsifier: 0.5 parts by weight alkylarylpolyglycolether
To produce a suitable preparation of the active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of spore suspension the spores are diluted with emulsifier- containing water to the desired concentration.
Maize {Zea mais) leaf sections are sprayed with a preparation of the active ingredient of the desired concentration. Once dry, the leaf sections are infested with fall armyworm larvae {Spodoptera frugiperda).
After the specified period of time, mortality in % is determined. 100% means all caterpillars have been killed and 0% means none of the caterpillars have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table E: Spodoptera frugiperda - test
Figure imgf000065_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example F
Spodoptera frugiperda -test (SPODFR)
Solvent: 7 parts by weight of dimethylformamide
Emulsifier: 1 part by weight of alkylaryl polyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration. Ammonium salt and/or penetration enhancer in a dosage of 1000 ppm are added to the desired concentration if necessary.
Maize leaves {Zea mais) are treated by being sprayed with the preparation of the active compound of the desired concentration and are infested with caterpillars of the fall army worm {Spodoptera frugiperda). The mortality values determined thus are recalculated using the Colby-formula (see above). After the specified period of time, mortality in % is determined. 100 % means all the caterpillars have been killed; 0 % means none of the caterpillars have been killed.
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table F: Spodoptera frugiperda
Figure imgf000066_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example G
Myzus persicae - spray test
Solvent: 78.0 parts by weight acetone
1.5 parts by weight dimethylformamide
Emulsifier: 0.5 parts by weight alkylarylpolyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration.
Chinese cabbage (Brassica pekinensis) leaf- disks infected with all instars of the green peach aphid {Myzus persicae) are sprayed with a preparation of the active ingredient of the desired concentration. After the specified period of time, mortality in % is determined. 100 % means all aphids have been killed; 0 % means none of the aphids have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above).
According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds: - -
Table G-l : Myzus persicae
Active Ingredient Concentration Efficacy in g ai/ha in % after Id
Requiem (QRD 4.052) 400 0
Imidacloprid (1144) 0.16 70
Requiem + Imidacloprid obs.* cal.** (2500 : 1) 400 + 0.16 90 70 according to the invention
Thiamethoxam (1147) 0.8 70
Requiem + Thiamethoxam obs.* cal.** (500 : 1) 400 + 0.8 90 70 according to the invention
Table G-2: Myzus persicae - test
Active Ingredient Concentration Efficacy in g ai/ha in % after 6d
Requiem (QRD 4.052) 400 0
Cyantraniliprole (1232) 0.8 0
Requiem + Cyantraniliprole obs.* cal.** (500 : 1) 400 + 0.8 70 0 according to the invention
B-Cyfluthrin (I105) 0.16 0
Requiem + B-Cyfluthrin obs.* cal.** (2500 : 1) 400 + 0.16 70 0 according to the invention
Flupyradiiurone (1262) 0.8 0
Requiem + Flupyradiiurone obs.* cal.** (500 : 1) 400 + 0.8 70 0 according to the invention
Methiocarb (115) 500 0
Requiem + Methiocarb obs.* cal.** (1 : 1.25) 400 + 500 90 0 according to the invention
Spirotetramat (1223) 0.8 0
Requiem + Spirotetramat obs.* cal.** (500 : 1) 400 + 0.8 70 0 - 7 -
Figure imgf000068_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula
Example H
Tetranychus urticae - spray test, OP-resistant
Solvent: 78.0 parts by weight acetone
1.5 parts by weight dimethylformamide
Emulsifier: 0.5 parts by weight alkylarylpolyglycolether
To produce a suitable preparation of active compound, 1 part by weight of active compound is mixed with the stated amount of solvent and emulsifier, and the concentrate is diluted with emulsifier- containing water to the desired concentration. To produce a suitable preparation of a spore suspension the spores are diluted with emulsifier- containing water to the desired concentration.
French beans (Phaseolus vulgaris) which are heavily infested with all stages of the two spotted spidermite (Tetranychus urticae), are sprayed with a preparation of the active ingredient of the desired concentration.
After the specified period of time, mortality in % is determined. 100% means all spider mites have been killed and 0% means none of the spider mites have been killed. The mortality values determined thus are recalculated using the Colby- formula (see above). According to the present application in this test e.g. the following combinations show a synergistic effect in comparison to the single compounds:
Table H-1 : Tetranychus urticae - test
Active Ingredient Concentration Efficacy
in g ai/ha in % after 2d
Requiem (QRD 4.052) 400 0
Spinetoram (1150) 4 20
Requiem + Spinetoram obs.* cal.**
(100 : 1) 400 + 4 70 20
according to the invention
Spinosad (1151) 4 0
Requiem + Spinosad obs.* cal.**
(100 : 1) 400 + 4 20 0
according to the invention
Table H-2: Tetranychus urticae - test
Active Ingredient Concentration Efficacy
in g ai/ha in % after 6d
Requiem (QRD 4.052) 400 0
(1277) 4 70
Requiem + (1277) obs.* cal.**
(100 : 1) 400 + 4 100 70
according to the invention
B-Cyfluthrin (I105) 4 0
Requiem + B-Cyfluthrin obs.* cal.**
(100 : 1) 400 + 4 70 0
according to the invention
Deltamethrin (I116) 4 0
Requiem + Deltamethrin obs.* cal.**
(100 : 1) 400 + 4 70 0
according to the invention
Methiocarb (115) 100 20
Requiem + Methiocarb obs.* cal.**
(4 : 1) 400 + 100 70 20
according to the invention
Spiromesifen (1222) 0.8 30 - -
Figure imgf000070_0001
obs. = observed insecticidal efficacy, ** cal. = efficacy calculated with Colby-formula

Claims

A composition comprising a) a pesticidal terpene mixture comprising, as pesticidally active chemical compounds, a-terpinene, p-cymene and limonene, and b) at least one insecticide selected from the group consisting of
Abamectin, Acephate, Acetamiprid, Acrinathrin, Afidopyropen, Alpha-Cypermethrin, Azadirachtin, Bacillus firmus, Beta-Cyfluthrin, Bifenthrin, Buprofezin, Clothianidin, Chlorantraniliprole, Chlorfenapyr, Chlorpyrifos, Carbofuran, Cyantraniliprole, Cyenopyrafen, Cyflumentofen, Cyfluthrin, Cypermethrin, Deltamethrin, Diafenthiuron, Dinotefuran, Emamectin- benzoate, Ethiprole, Fenpyroximate, Fipronil, Flometoquin, Flonicamid, Flubendiamide, Fluensulfone, Fluopyram, Flupyradiiurone, Gamma-Cyhalothrin, Imidacloprid, Indoxacarb, Lambda-Cyhalothrin, Lufenuron, Metaflumizone, Methiocarb, Methoxyfenozide, Milbemectin, Profenofos, Pyflubumide, Pymetrozine, Pyrifluquinazone, Spinetoram, Spinosad, Spirodiclofen, Spiromesifen, Spirotetramate, Sulfoxaflor, Tebufenpyrad, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, Triflumuron, l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-
(methylcarbamoyl)phenyl]-3 - { [5-(trifluoromethyl)- 1 H-tetrazol- 1 -yljmethyl} - 1 H-pyrazole-5- carboxamide, l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)-2H-tetrazol-2-yl]methyl} - 1 H-pyrazole-5-carboxamide and 1 - {2-fluoro-4- methyl-5-[(2,2,2-trifluorethyl)sulfinyl]phenyl}-3-(trifluoromethyl)-lH-l,2,4-triazol-5-amine , in a synergistically effective amount.
The composition according to claim 1 , further comprising at least one fungicide, preferably in a synergistically effective amount, with the proviso that the pesticidal terpene mixture and the fungicide are not identical.
The composition according to claim 1 or 2, wherein the insecticide b) is selected from the group consisting of Abamectin, Beta-Cyfluthrin, Clothianidin, Chlorantraniliprole, Cyantraniliprole, Deltamethrin, Fipronil, Flubendiamide, Flupyradiiurone, Imidacloprid, Methiocarb, Sulfoxaflor, Spinetoram, Spinosad, Spiromesifen, Spirotetramate, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, a mixture of l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6- (methylcarbamoyl)phenyl]-3 - { [5-(trifluoromethyl)-2H-tetrazol-2-yl]methyl} - 1 H-pyrazole-5- carboxamide and 1 -(3 -chloropyridin-2-yl)-N- [4-cyano-2-methyl-6-(methylcarbamoyl)phenyl] -3 - { [5-(trifluoromethyl)- 1 H-tetrazol- 1 -yl]methyl} - 1 H-pyrazole-5-carboxamide, and 1 - {2-fluoro-4- methyl-5-[(2,2,2-trifluorethyl)sulfinyl]phen^
4. The composition according to any of claims 1 to 3, wherein the fungicide is a synthetic fungicide.
5. The composition according to any one of claims 1 to 4, wherein the pesticidal terpene mixture consists of a-terpinene, p-cymene and Iimonene and accidental impurities.
6. The composition according to any one of claims 1 to 5, wherein the pesticidal terpene mixture comprises a simulated blend of an essential oil extract of Chenopodium ambrosioides near ambrosioides, wherein the simulated blend consists essentially of substantially pure a-terpinene, p-cymene and Iimonene, wherein each of the substantially pure α-terpinene, p-cymene and Iimonene is not obtained from a Chenopodium extract.
7. The composition according to any of claims 1 to 6, comprising as pesticdal terpene mixture an insecticidally effective amount of
(i) a simulated blend of an essential oil extract of Chenopodium ambrosioides near ambrosioides, wherein the simulated blend consists essentially of a volume filler and substantially pure a- terpinene, p-cymene, and Iimonene, wherein each of the substantially pure α-terpinene, p-cymene and Iimonene is not obtained from a Chenopodium extract and
(ii) a carrier.
8. A composition of any of claims 1 to 7 wherein the relative ratio by weight of the α-terpinene to p- cymene to Iimonene is about 30 to about 70 α-terpinene, about 10 to about 30 p-cymene and about 1 to about 20 Iimonene.
9. A composition according to any of claims 1 to 8 using a pesticidally active terpene mixture which is obtaianble by synthetically producing the α-terpinene and p-cymene, obtaining the Iimonene from a plant other than Chenopodium, and mixing. The composition according to any one of claims 2 to 9, wherein the fungicide is selected from the group consisting of inhibitors of the ergosterol biosynthesis, inhibitors of the respiratory chain at complex I or II, inhibitors of the respiratory chain at complex III, inhibitors of the mitosis and cell division, compounds capable to induce a host defence, inhibitors of the amino acid and/or protein biosynthesis, inhibitors of the ATP production, inhibitors of the cell wall synthesis, inhibitors of the lipid and membrane synthesis, inhibitors of the melanine biosynthesis, inhibitors of the nucleic acid synthesis, inhibitors of the signal transduction, compounds capable to act as an uncoupler such as binapacryl, dinocap, ferimzone, fluazinam, meptyldinocap and further compounds, like for example benthiazole, bethoxazin, capsimycin, carvone, chinomethionat, pyriofenone (chlazafenone), cufraneb, cyflufenamid, cymoxanil, cyprosulfamide, dazomet, debacarb, dichlorophen, diclomezine, difenzoquat, difenzoquat methylsulphate, diphenylamine, ecomate, fenpyrazamine, flumetover, fluoroimide, flusulfamide, flutianil, fosetyl-aluminium, fosetyl- calcium, fosetyl-sodium, hexachlorobenzene, irumamycin, methasulfocarb, methyl isothiocyanate, metrafenone, mildiomycin, natamycin, nickel dimethyldithiocarbamate, nitrothal-isopropyl, octhilinone, oxamocarb, oxyfenthiin, pentachlorophenol and salts, phenothrin, phosphorous acid and its salts, propamocarb-fosetylate, propanosine-sodium, proquinazid, pyrimorph, (2E)-3-(4- tert-butylphenyl)-3-(2-chloropyridin-4-yl)-l -(morpholin-4-yl)prop-2-en-l-one, (2Z)-3-(4-tert- butylphenyl)-3 -(2-chloropyridin-4-yl)- 1 -(morpholin-4-yl)prop-2-en- 1 -one, pyrrolnitrine, tebufloquin, tecloftalam, tolnifanide, triazoxide, trichlamide, zarilamid, (3S,6S,7R,8R)-8-benzyl- 3 - [( {3 - [(isobutyryloxy)methoxy] -4-methoxypyridin-2-yl} carbonyl)amino] -6-methyl-4,9-dioxo- 1 ,5-dioxonan-7-yl 2-methylpropanoate, 1 -(4- {4-[(5R)-5-(2,6-difluorophenyl)-4,5-dihydro- 1 ,2- oxazol-3 -yl] - 1 ,3 -thiazol-2-yl} piperidin- 1 -yl)-2- [5-methyl-3 -(trifluoromethyl)- 1 H-pyrazol- 1 - yl]ethanone, l-(4- {4-[(5S)-5-(2,6-difluorophenyl)-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2- yl}piperidin-l -yl)-2-[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l-yl]ethanone, l-(4- {4-[5-(2,6- difluorophenyl)-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l -yl)-2-[5-methyl-3- (trifluoromethyl)- 1 H-pyrazol- 1 -yl] ethanone, 1 -(4-methoxyphenoxy)-3 ,3 -dimethylbutan-2-yl 1 H- imidazole-l-carboxylate, 2,3,5,6-tetrachloro-4-(methylsulfonyl)pyridine, 2,3-dibutyl-6- chlorothieno[2,3-d]pyrimidin-4(3H)-one, 2,6-dimethyl-lH,5H-[l,4]dithiino[2,3-c:5,6- c']dipyrrole-l,3,5,7(2H,6H)-tetrone, 2-[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l -yl]-l-(4- {4- [(5R)-5-phenyl-4,5-dihydro-l,2-oxazol-3-yl]-l,3-thiazol-2-yl}piperidin-l-yl)ethanone, 2-[5- methyl-3 -(trifluoromethyl)- 1 H-pyrazol- 1 -yl]- 1 -(4- {4-[(5S)-5-phenyl-4,5-dihydro- 1 ,2-oxazol-3 - yl] - 1 ,3 -thiazol-2-yl} piperidin- 1 -yl)ethanone, 2- [5-methyl-3 -(trifluoromethyl)- 1 H-pyrazol- 1 -yl] - 1 - {4-[4-(5-phenyl-4,5-dihydro-l,2-oxazol-3-yl)-l,3-thiazol-2-yl]piperidin-l-yl} ethanone, 2-butoxy- 6-iodo-3-propyl-4H-chromen-4-one, 2-chloro-5-[2-chloro-l-(2,6-difluoro-4-methoxyphenyl)-4- methyl-lH-imidazol-5-yl]pyridine, 2-phenylphenol and salts, 3-(4,4,5-trifluoro-3,3-dimethyl-3,4- dihydroisoquinolin-l-yl)quinolone, 3,4,5-trichloropyridine-2,6-dicarbonitrile, 3-[5-(4- chlorophenyl)-2,3-dimethyl-l,2-oxazolidin-3-yl]pyridine, 3-chloro-5-(4-chlorophenyl)-4-(2,6- difluorophenyl)-6-methylpyridazine, 4-(4-chlorophenyl)-5-(2,6-difluorophenyl)-3,6- dimethylpyridazine, 5-amino- 1 ,3,4-thiadiazole-2-thiol, 5-chloro-N'-phenyl-N'-(prop-2-yn- 1 - yl)thiophene-2-sulfonohydrazide, 5-fluoro-2-[(4-fluorobenzyl)oxy]pyrimidin-4-amine, 5-fluoro-2- [(4-methylbenzyl)oxy]pyrimidin-4-amine, 5-methyl-6-octyl[l,2,4]triazolo[l,5-a]pyrimidin-7- amine, ethyl (2Z)-3-amino-2-cyano-3-phenylprop-2-enoate, N'-(4- {[3-(4-chlorobenzyl)-l,2,4- thiadiazol-5-yl] oxy} -2,5-dimethylphenyl)-N-ethyl-N-methylimidoformamide, N-(4- chlorobenzyl)-3-[3-methoxy-4-(prop-2-yn-l-yloxy)phenyl]propanamide, N-[(4- chlorophenyl)(cyano)methyl]-3-[3-methoxy-4-(prop-2-yn-l-yloxy)phenyl]propanamide, N-[(5- bromo-3-chloropyridin-2-yl)methyl]-2,4-dichloropyridine-3-carboxamide, N-[l-(5-bromo-3- chloropyridin-2-yl)ethyl]-2,4-dichloropyridine-3-carboxamide, N-[l-(5-bromo-3-chloropyridin-2- yl)ethyl]-2-fluoro-4-iodopyridine-3-carboxamide, N- {(E)-[(cyclopropylmethoxy)imino] [6-
(difluoromethoxy)-2,3-difluorophenyl]methyl} -2-phenylacetamide, N- {(Z)-
[(cyclopropylmethoxy)imino] [6-(difluoromethoxy)-2,3 -difluorophenyl]methyl} -2- phenylacetamide, N'- {4-[(3 -tert-butyl-4-cyano- 1 ,2-thiazol-5-yl)oxy] -2-chloro-5-methylphenyl} - N-ethyl-N-methylimidoformamide, N-methyl-2-(l- {[5-methyl-3-(trifluoromethyl)-lH-pyrazol-l- yl]acetyl}piperidin-4-yl)-N-(l ,2,3,4 etrahydronaphthalen-l-yl)-l,3-thiazole-4-carboxamide, N- methyl-2-( 1 - { [5 -methyl-3 -(trifluoromethyl)- 1 H-pyrazol- 1 -yl] acetyl} piperidin-4-yl)-N- [( 1 R)- 1 ,2,3 ,4-tetrahydronaphthalen- 1 -yl] - 1 ,3 -thiazole-4-carboxamide, N-methyl-2-( 1 - { [5-methyl-3 - (trifluoromethyl)- 1 H-pyrazol- 1 -yl] acetyl} piperidin-4-yl)-N- [(1S)-1 ,2,3 ,4-tetrahydronaphthalen- 1 - yl]-l,3-thiazole-4-carboxamide, pentyl {6-[({[(l-methyl-lH-tetrazol-5- yl)(phenyl)methylidene]amino}oxy)methyl]pyridin-2-yl}carbamate, phenazine-l-carboxylic acid, quinolin-8-ol, quinolin-8-ol sulfate (2: 1), tert-butyl {6-[({[(l-methyl-lH-tetrazol-5- yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, l-methyl-3-(trifluoromethyl)- N-[2'-(trifluoromethyl)biphenyl-2-yl]-lH-pyrazole-4-carboxamide, N-(4'-chlorobiphenyl-2-yl)-3- (difluoromethyl)- 1 -methyl- 1 H-pyrazole-4-carboxamide, N-(2',4'-dichlorobiphenyl-2-yl)-3 -
(difluoromethyl)-l -methyl- lH-pyrazole-4-carboxamide, 3-(difluoromethyl)-l-methyl-N-[4'- (trifluoromethyl)biphenyl-2-yl]-lH-pyrazole-4-carboxamide, N-(2',5'-difluorobiphenyl-2-yl)-l- methyl-3 -(trifluoromethyl)- 1 H-pyrazole-4-carboxamide, 3 -(difluoromethyl)- 1 -methyl-N- [4'- (prop- 1 -yn- 1 -yl)biphenyl-2-yl]- 1 H-pyrazole-4-carboxamide, 5-fluoro- 1 ,3-dimethyl-N- [4'-(prop- 1 - yn- 1 -yl)biphenyl-2-yl] - 1 H-pyrazole-4-carboxamide, 2-chloro-N- [4'-(prop- 1 -yn- 1 -yl)biphenyl-2- yl]pyridine-3-carboxamide, 3-(difluoromethyl)-N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2-yl]- 1 -methyl- lH-pyrazole-4-carboxamide, N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2-yl]-5-fluoro- 1 ,3-dimethyl- 1 H-pyrazole-4-carboxamide, 3 -(difluoromethyl)-N-(4'-ethynylbiphenyl-2-yl)- 1 - methyl- 1 H-pyrazole-4-carboxamide, N-(4'-ethynylbiphenyl-2-yl)-5-fluoro- 1 ,3-dimethyl- 1 H- pyrazole-4-carboxamide, 2-chloro-N-(4'-ethynylbiphenyl-2-yl)pyridine-3-carboxamide, 2-chloro- N-[4'-(3,3-dimethylbut-l-yn-l-yl)biphenyl-2-yl]pyridine-3-carboxamide, 4-(difluoromethyl)-2- methyl-N-[4'-(trifluoromethyl)biphenyl-2-yl]-l,3-thiazole-5-carboxamide, 5-fluoro-N-[4'-(3- hydroxy-3 -methylbut- 1 -yn- 1 -yl)biphenyl-2-yl] - 1 ,3 -dimethyl- 1 H-pyrazole-4-carboxamide, 2- chloro-N- [4'-(3 -hydroxy-3 -methylbut- 1 -yn- 1 -yl)biphenyl-2-yl]pyridine-3 -carboxamide, 3 -
(difluoromethyl)-N- [4'-(3 -methoxy-3 -methylbut- 1 -yn- 1 -yl)biphenyl-2-yl] - 1 -methyl- 1 H-pyrazole- 4-carboxamide, 5-fluoro-N-[4'-(3-methoxy-3-methylbut-l-yn-l-yl)biphenyl-2-yl]-l,3-dimethyl- lH-pyrazole-4-carboxamide, 2-chloro-N-[4'-(3 -methoxy-3 -methylbut- 1-yn-l -yl)biphenyl-2- yl]pyridine-3 -carboxamide, (5-bromo-2-methoxy-4-methylpyridin-3-yl)(2,3,4-trimethoxy-6- methylphenyl)methanone, N-[2-(4- {[3-(4-chlorophenyl)prop-2-yn-l -yl]oxy} -3- methoxyphenyl)ethyl]-N2-(methylsulfonyl)valinamide 4-oxo-4-[(2-phenylethyl)amino]butanoic acid, but-3-yn-l-yl {6-[({[(Z)-(l-methyl-lH-tetrazol-5- yl)(phenyl)methylene]amino}oxy)methyl]pyridin-2-yl}carbamate, 4-Amino-5-fluorpyrimidin-2- ol, propyl 3,4,5-trihydroxybenzoate and oryzastrobin.
11. The composition according to any one of claims 1 to 10 additionally comprising at least one auxiliary selected from the group consisting of extenders, solvents, spontaneity promoters, carriers, emulsifiers, dispersants, frost protectants, thickeners and adjuvants.
The composition according to any of claim 1 to 11 , with the proviso that the combination consisting only of the pesticidal terpene mixture and Flonicamid (Beleaf®) as active ingredients is excluded.
13. The composition according to any of claims 1 to 11, with the proviso that the combination consisting only of the pesticidal terpene mixture and Pymetrozine (Fulfill®) as active ingredients is excluded.
14. A use of the composition according to any one of claims 1 to 13 as insecticide and/or fungicide.
15. The use according to claim 14 for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens.
16. The use according to claim 14 or 15 for treating conventional or transgenic plants or seed thereof.
17. A method for reducing overall damage of plants and plant parts as well as losses in harvested fruits or vegetables caused by insects, mites, nematodes and/or phytopathogens comprising the step of simultaneously or sequentially applying a pesticidal terpene mixture comprising, as pesticidally active chemical compounds, a-terpinene, p-cymene and limonene, and at least one insecticide selected from the group consisting of Abamectin, Acephate, Acetamiprid, Acrinathrin, Afidopyropen, Alpha-Cypermethrin, Azadirachtin, Bacillus firmus, Beta-Cyfluthrin, Bifenthrin, Buprofezin, Clothianidin, Chlorantraniliprole, Chlorfenapyr, Chlorpyrifos, Carbofuran, Cyantraniliprole, Cyenopyrafen, Cyflumentofen, Cyfluthrin, Cypermethrin, Deltamethrin, Diafenthiuron, Dinotefuran, Emamectin-benzoate, Ethiprole, Fenpyroximate, Fipronil, Flometoquin, Flonicamid, Flubendiamide, Fluensulfone, Fluopyram, Flupyradifurone, γ-Cyhalothrin, Imidacloprid, Indoxacarb, Lambda-Cyhalothrin, Lufenuron, Metaflumizone, Methiocarb, Methoxyfenozide, Milbemectin, Profenofos, Pyflubumide, Pymetrozin, Pyrifluquinazone, Spinetoram, Spinosad, Spirodiclofen, Spiromesifen, Spirotetramate, Sulfoxaflor, Tebufenpyrad, Tefluthrin, Thiacloprid, Thiamethoxam, Thiodicarb, Triflumuron, l-(3-chloropyridin-2-yl)-N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5- (trifluoromethyl)- 1 H-tetrazol- 1 -yljmethyl} - 1 H-pyrazole-5-carboxamide, 1 -(3-chloropyridin-2-yl)- N-[4-cyano-2-methyl-6-(methylcarbamoyl)phenyl]-3- {[5-(trifluoromethyl)-2H-tetrazol-2- yl]methyl}-lH-pyrazole-5-carboxamide and l- {2-fluoro-4-methyl-5-[(2,2,2- trifluorethyl)sulfinyl]phenyl} -3-(trifluoromethyl)- 1 H- 1 ,2,4-triazol-5-amine, in a synergistically effective amount and optionally at least one fungicide, preferably in a synergistically effective amount, on the plant, plant parts, harvested fruits, vegetables and/or plant's locus of growth.
18. The method of claim 17, with the proviso that it does not include
- the sequential treatment, in particular of watermelon seedlings, comprising separate treatment with the pesticidal terpene mixture as defined in any of claims 1 and 4 to 8 and the specific insecticides and fungicides 2x Pymetrozine (Fulfill®), 2x Endosulfan (Thionex®), 2x Spiromesifen (Oberon®), 2x Endosulfan (Thionex®), as disclosed in Example 5 of WO 2010/144919, - the sequential treatment, in particular of S. tuberosum, using the pesticidal terpene mixture as defined in any of claims 1 and 4 to 8 every 3 to 4 days and the standard sequence using Acetamipirid (Assail®), Flonicamid (Beleaf®), Pymetrozine (Fulfill®), Imidacloprid (Provado®), Acetamipirid (Assail®), Methamidophos (Monitor®) disclosed in Example 6 of WO 2010/144919
- the sequential treatment, in particular of "Jalapeno" pepper transplants, using the pesticidal terpene mixture of any of claims 1 and 4 to 8 and Spinetoram-J and Spinetoram-L (Radiant®) disclosed in Example 14 of WO 2010/144919;
19. The method according to claim 17 or 18, wherein the optional fungicide is a synthetic fungicide.
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CN103891749A (en) * 2014-04-22 2014-07-02 陕西上格之路生物科学有限公司 Insecticidal combination containing sulfoxaflore and metaflumizone
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