WO2023189782A1 - Plant disease control composition, preparation, and plant disease control method - Google Patents

Plant disease control composition, preparation, and plant disease control method Download PDF

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WO2023189782A1
WO2023189782A1 PCT/JP2023/010760 JP2023010760W WO2023189782A1 WO 2023189782 A1 WO2023189782 A1 WO 2023189782A1 JP 2023010760 W JP2023010760 W JP 2023010760W WO 2023189782 A1 WO2023189782 A1 WO 2023189782A1
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plant
plant disease
disease control
control composition
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PCT/JP2023/010760
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French (fr)
Japanese (ja)
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友紀子 瀧口
豪 寺岡
憲太朗 山本
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株式会社Mmag
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, 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
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/34Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
    • A01N43/40Biocides, 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
    • A01N43/42Biocides, 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 condensed with carbocyclic rings
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • A01N43/80Biocides, 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 1,2
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72Biocides, 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
    • A01N43/82Biocides, 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 three ring hetero atoms
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N65/00Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N65/00Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
    • A01N65/03Algae
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01PBIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
    • A01P3/00Fungicides

Definitions

  • the present disclosure relates to a plant disease control composition, a formulation, and a plant disease control method.
  • Rice blast is the most damaging disease in rice cultivation caused by the rice blast fungus (Pyricularia oryzae), and many control agents using fungicidal compounds have been reported so far.
  • Non-Patent Document 1 discloses that compositions using tebufloquine, which is one of the bactericidal ingredients (for example, Patent Documents 1 to 5), there is no disclosure whatsoever about a mixture using tebufloquine and a resistance inducer in combination. .
  • Patent Document 1 Japanese Patent Application Publication No. 2003-55114 Patent Document 2: International Publication No. 2004/039156 Patent Document 3: International Publication No. 2006/106811 Patent Document 4: Japanese Patent Application Publication No. 2011-201858 Patent Document 5: Japanese Patent Application Publication No. 2011-201858 Publication No. 2007-112760
  • Non-patent document 1 Latest trends in drug-resistant bacteria research and strengthening of countermeasures, Journal of the Japanese Society of Pesticides, No. 39, Volume 1, pp. 53-57, 2014
  • the problem to be solved by an embodiment of the present disclosure is to exhibit an excellent control effect on plant diseases compared to a plant disease control composition containing tebufloquine alone as an active ingredient, and to reduce the amount of the drug applied.
  • An object of the present invention is to provide a plant disease control composition that reduces environmental burden.
  • a problem to be solved by other embodiments of the present disclosure is to provide a formulation using a plant disease control composition and a method for controlling plant diseases.
  • tebufloquine and a plant resistance inducer exhibit synergistic plant disease control effects, and have completed the present invention. That is, specific means for solving the problem include the following aspects.
  • a plant disease control composition containing tebufloquine and a plant resistance inducer as active ingredients (2) The plant disease control composition according to (1), wherein the plant disease is rice blast disease. (3) The plant resistance inducer is jasmonic acid, salicylic acid, probenazole, isotianil, tiadinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, The plant disease control composition according to (1), comprising at least one selected from fosetyl, phosphorous acid or a salt thereof, and a compound represented by the following formula (I).
  • X 1 and X 4 each independently represent a hydrogen atom, a fluorine atom, a chlorine atom, or a trifluoromethyl group
  • X 2 and X 3 each independently represent a hydrogen atom, a fluorine atom, Represents a chlorine atom or a methyl group
  • A is a halogen atom, a hydroxyl group, an amino group, a methylthio group, an alkyl group having 1 to 4 carbon atoms optionally substituted with 1 to 3 halogen atoms, 1 to 3 Alkyloxy group having 1 to 4 carbon atoms which may be substituted with a halogen atom, alkylcarbonyl group having 1 to 4 carbon atoms, methoxycarbonyl group, ethoxycarbonyl group, benzylaminocarbonyl group, acetoxy group, nitro group, cyano group represents a phenyl group optionally substituted with 1 to 5 groups selected from the group consisting of
  • a formulation comprising the plant disease control composition according to any one of (1) to (3).
  • the formulation according to (4) is selected.
  • (6) A method for controlling plant diseases, which comprises applying the plant disease control composition according to any one of (1) to (3) to plant diseases.
  • the method for controlling a plant disease according to (6), wherein the plant disease is a rice blast disease.
  • a plant disease control composition containing tebufloquine alone as an active ingredient compared to a plant disease control composition containing tebufloquine alone as an active ingredient, it exhibits superior control effects against plant diseases, and also reduces the amount of application of the drug and causes environmental burden.
  • a plant disease control composition that aims at alleviating.
  • formulations and methods for controlling plant diseases using plant disease control compositions are provided.
  • indicating a numerical range is used to include the numerical values written before and after it as the lower limit and upper limit.
  • the upper limit value or lower limit value described in one numerical range may be replaced with the upper limit value or lower limit value of another numerical range described step by step. good. Further, in the numerical ranges described in this specification, the upper limit or lower limit of the numerical range may be replaced with the value shown in the Examples.
  • the amount of each component in the target object is the amount of the multiple types of substances present in the target object. means the total content rate or amount of
  • One embodiment of the present disclosure relates to a plant disease control composition containing tebufloquine and a plant resistance inducer as active ingredients.
  • Plant resistance inducers as used herein are substances that do not exhibit direct antibacterial activity against plant pathogens, or substances that exhibit some antibacterial activity but whose activity is not the main activity against plant pathogens that require control. means. More specifically, a plant resistance inducer refers to a substance classified by the Fungicide Resistance Control Committee (FRAC) as mode of action P (induction of host plant resistance) in the FRAC code table.
  • FRAC Fungicide Resistance Control Committee
  • the plant disease control composition according to the present disclosure improves fungicidal action and induces resistance by applying a fungicide that does not have a sufficient control effect on plant diseases alone in combination with a compound having a different action. It has a synergistic effect, can efficiently control plant diseases such as rice blast, and can reduce the number of times of spraying of fungicidal agents. Moreover, the plant disease control composition according to the present disclosure can reduce the risk of emergence of fungicide-resistant bacteria. Furthermore, the plant disease control composition according to the present disclosure can reduce the amount of fungicide applied per cropping season, thereby reducing the environmental load.
  • the plant disease control composition according to the present disclosure makes a significant contribution to stabilizing agricultural production and protecting the environment.
  • the plant resistance inducers in the present disclosure include jasmonic acid, salicylic acid, probenazole, isotianil, tiadinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, Examples include, but are not limited to, fosetyl, phosphorous acid and its salts, and the compound represented by the following formula (I).
  • X 1 and X 4 each independently represent a hydrogen atom, a fluorine atom, a chlorine atom, or a trifluoromethyl group
  • X 2 and X 3 each independently represent a hydrogen atom, a fluorine atom, Represents a chlorine atom or a methyl group
  • A is a halogen atom, a hydroxyl group, an amino group, a methylthio group, an alkyl group having 1 to 4 carbon atoms optionally substituted with 1 to 3 halogen atoms, 1 to 3 Alkyloxy group having 1 to 4 carbon atoms which may be substituted with a halogen atom, alkylcarbonyl group having 1 to 4 carbon atoms, methoxycarbonyl group, ethoxycarbonyl group, benzylaminocarbonyl group, acetoxy group, nitro group, cyano group represents a phenyl group which may be substituted with 1 to 5 groups selected from the group consisting of
  • a specific example of the compound represented by formula (I) is 2,6-difluoro-N-(3-methoxyphenyl)-4-Pyridinecarboxamide (CAS number: 2244744-34-9. Hereinafter also referred to as compound A). can be mentioned.
  • Preferred plant resistance inducers include probenazole, isotianil, thiazinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, and 2,6-difluoro-N-(3-methoxyphenyl)-4-pyridinecarboxamide (CAS number: 2244744). -34-9).
  • the mixing ratio of tebufloquine and plant resistance inducer in the plant disease control composition according to the present disclosure is preferably in the following range.
  • the plant resistance inducer combined with tebufloquine is probenazole, isotianil, tiazinil, dichlorbenziazox, acibenzolar S-methyl, or a compound represented by formula (I)
  • the mixing ratio by mass is 1:1:1: Therefore, it is preferable that the amount of the plant resistance inducer to be combined is 0.0001 to 10.
  • the mass ratio The mixing ratio is preferably 1:1 for tebufloquine and 0.0001 to 100:0 for the combined plant resistance inducer.
  • the mixing ratio by mass ratio is such that when the plant resistance inducer to be combined with tebufloquine is probenazole, isotianil, tiazinyl, dichlorbenziazox, acibenzolar S-methyl, or a compound represented by formula (I), tebufloquine is mixed with tebufloquine. is 1 to 0.01 to 10 for the combined plant resistance inducer, and when the plant resistance inducer to be combined with tebufloquine is laminarin, the ratio for tebufloquin is 1 to 0.1 to 10 for laminarin.
  • Examples of plant pathogens to be controlled by the plant disease control composition according to the present disclosure include fungi, bacteria, viruses, and the like. However, it is not limited to these. Examples of fungi include plant pathogenic fungi, examples of bacteria include plant pathogenic bacteria, and examples of viruses include plant pathogenic viruses.
  • plant pathogenic fungi examples include Alternaria alternata, Alternaria kikutiana, Botrytis cinerea, and Cochliobolus cinerea. miyabeanus), potato anthracnose (Colletotrichum atramentarium), cucumber anthracnose (Colletotrichum lagenarium), cucumber vine splitting fungus (Fusarium oxysporum f. sp. lycopersici, Gibberella fujikuroi, Glomerella cingulata, and Glomerella cingulata.
  • preferred plant pathogenic fungi for which the plant disease control composition according to the present disclosure has a particularly good effect as a control target include rice sesame leaf blight fungi, rice bakanae fungi, and rice blast fungi. , rice seedling blight disease fungi, and rice sheath blight disease fungi, and more preferred plant pathogenic fungi include rice blast fungi.
  • examples of plant pathogenic bacteria include Pseudomonas, Erwinia, Pectobacterium, Xanthomonas, Burkholderia, Streptomyces, Ralstonia, Clavibacter, and Rhizoma.
  • nas genus, Agrobacterium genus, Bacillus genus, Clostridium genus, Curtobacterium genus, Pantoea Examples include bacteria of the genera Acidovorax, Arthrobacter, and Rhodococcus.
  • plant pathogenic viruses include, for example, Soil-borne wheat mosaic virus, Soybean mosaic virus, Alfalfa mosaic virus, and Potato leaf curl virus.
  • Plant leaf roll virus examples include Cucumber mosaic virus and Tobacco mosaic virus.
  • the plant disease control composition according to the present disclosure may be used as is. Further, a preparation containing the plant disease control composition according to the present disclosure can be made into any dosage form according to a conventional method.
  • the dosage form of the preparation may be a wettable powder, an emulsion, a flowable preparation, a granule wettable powder, a dry flowable preparation, a powder, a DL powder, an FD powder, or a microcapsule.
  • the formulation is an agrochemical formulation used as an agrochemical.
  • DL powder refers to a formulation that suppresses scattering and has an average particle size of 20 ⁇ m or more and 20% or less of particles with a particle size of 10 ⁇ m or less.
  • FD powder is a formulation that utilizes scattering and has an average particle size of 5 ⁇ m or less.
  • the plant disease prevention composition according to the present disclosure can further be used in all formulations such as granules, powders, jumbo granules, packs, and aerosols for use in water in Nissans and seedling boxes.
  • Agro-horticulturally acceptable additives include carriers, surfactants, binders, thickeners, antifreeze agents, colorants, adjuvants, and the like.
  • Carriers include solid carriers, liquid carriers, and gaseous carriers. Agrochemical formulations can be produced together with these additives by common production methods.
  • solid carriers examples include clays (clay, carrion, diatomaceous earth, bentonite, acid clay, etc.), synthetic hydrated silicon dioxide, talc, perlite, vermiculite, pumice, and other inorganic minerals (sericite, quartz, sulfur, activated carbon, Examples include fine powders and granules such as calcium carbonate, hydrated silica, titanium oxide, etc., synthetic polymers such as starch, lactose, vinyl chloride polymers, and polyurethane, and plant-derived materials such as wood flour.
  • liquid carriers examples include alcohols (methanol, ethanol, isopropanol, polyethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, glycerin, etc.), ketones (acetone, methyl ethyl ketone, etc.), aromatic hydrocarbons (benzyl Alcohol, benzene, toluene, xylene, ethylbenzene, methylnaphthalene, etc.), aliphatic hydrocarbons (paraffin, n-hexane, cyclohexane, kerosene, kerosene, etc.), ethers (diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diisopropyl ether, diethyl ether, dioxane, tetrahydrofuran, etc.), esters (propylene carbonate, ethyl acetate, butyl acetate, benzyl benzoate
  • gaseous carriers examples include LPG, air, nitrogen, carbon dioxide, and dimethyl ether.
  • the content of the carrier used in the plant disease control composition according to the present disclosure is usually 5% by mass to 99.9% by mass, preferably 10% by mass to 98% by mass. be.
  • Surfactants are used in a variety of applications, including emulsification, dispersion, penetration, and disintegration.
  • As the surfactant nonionic surfactants, anionic surfactants, etc. can be used.
  • nonionic surfactant polyoxyethylene alkyl ethers, polyoxyethylene styrylphenyl ethers, polyoxyethylene/polyoxypropylene Brook copolymers, (polyoxyethylene) sorbitan fatty acid esters, etc. are used.
  • anionic surfactant alkyl sulfate esters, alkyl (aryl) sulfonates, naphthalene sulfonic acid/formalin condensates, lignin sulfonates, polycarboxylic acid salts, etc. are used.
  • the amount of surfactant used in the plant disease control composition according to the present disclosure is usually 0.01% to 30% by mass, preferably 0.05% to 20% by mass. Mass%.
  • cellulose binders such as carboxymethyl cellulose salts and methyl cellulose, starch binders such as polyvinyl alcohol, gum arabic, and dextrin are used.
  • thickener an organic polymer thickener such as xanthan gum or an inorganic powder such as bentonite is used.
  • anti-freezing agent a glycol-based anti-freezing agent such as propylene glycol is used.
  • coloring agent for example, tar dyes such as Blue No. 1 and Red No. 2, and caramel dyes are used.
  • adjuvants can be added for the purpose of improving the physical properties of the formulation. For example, white carbon, calcium stearate, and isothiazolin-3-one derivatives are used as fungicides to improve fluidity.
  • the content in the formulation is not limited, but the content of the plant disease control composition in 100 parts by mass of the formulation is in the range of 0.01 part by mass to 90 parts by mass.
  • the mass part can be set appropriately from .
  • the preferred content of the plant disease control composition in the formulation is in the range of 0.1 parts by mass to 50 parts by mass.
  • the plant disease control composition according to the present disclosure does not limit the application amount, but includes, for example, the weather, environmental conditions, cultivation conditions, growth conditions, application timing, application method, and disease onset of the target area for plant disease control. It is possible to appropriately set the application amount depending on disease-causing factors such as the severity of the disease.
  • the effective amount of the plant disease control composition to be applied is preferably 0.01 g to 10 kg, more preferably 1 g to 5 kg per 10 ares.
  • the plant disease control composition according to the present disclosure can be used during all crop cultivation periods in which pesticides are normally used, that is, from pre-sowing to germination, seedling-raising, vegetative growth, and pre-harvesting. be able to.
  • a preferred method of using the plant disease control composition according to the present disclosure is that it can be used at any time during the rice cultivation period, from after germination to the seedling-raising period, rice cultivation, and before harvest.
  • a more preferred method of use is from the seedling-raising period to before harvest.
  • foliage spraying treatment on individual plants includes foliage spraying treatment on individual plants, seedling nursery box treatment, side row application using a paddy rice transplanter, water surface application to rice field water, spraying treatment on the soil surface, and soil surface treatment.
  • the plant disease control composition according to the present disclosure exhibits sufficient efficacy for plant disease control in any application.
  • the plant disease control composition according to the present disclosure can also be applied with a mixture of pest control agents such as insecticides, fungicides, acaricides, and herbicides. Furthermore, the plant disease control composition according to the present disclosure and the pest control agent described above can be applied separately at different times.
  • insecticides include, for example, acephate, dichlorvos, EPN, fenitrothion, fenamifos, prothiofos, profenofos, pyraclofos.
  • chlorpyrifos-methyl chlorpyrifos-methyl
  • chlorfenvinphos demeton, ethion, malathion, coumaphos, isoxathion, fenthion, diazione diazinon, thiodicarb ), aldicarb, oxamyl, propoxur, carbaryl, fenobucarb, ethiofencarb, phenothiocarb, pirimicarb ( pirimicarb), carbofuran, carbosulfan (carbosulfan), furathiocarb, hyquincarb, alanycarb, methomyl, benfuracarb, cartap, thiocyc lam), bensultap, dicofol, tetradifon (tetradifon), acrinathrin, bifenthrin, cycloprothrin, cyflu
  • the above-mentioned fungicides include, for example, strobosides such as azoxystrobin, kresoxim-methyl, trifloxystrobin, metominostrobin, and orysastrobin.
  • Bilurin compound mepanipyrim Anilinopyrimidine compounds such as mepanipyrim, pyrimethanil, cyprodinil; triadimefon, bitertanol, triflumizole, meth Conazole (metconazole), propiconazole (propiconazole) , penconazole, flusilazole, myclobutanil, cyproconazole, tebuconazole, hexaconazole Azole compounds such as zole, prochloraz, and simeconazole ; quinoxaline compounds such as chinomethionate; dithiocarbamate compounds such as maneb, zineb, mancozeb, polycarbamate, propineb substance
  • zolin dicarboximide compounds such as flutolanil, mepronil, furametpyr, thifluzamide, boscalid, penthiopyrad; Xyanilide compound; fenpropimorph Morpholine compounds such as (fenpropimorph) and dimethomorph; Organotin compounds such as triphenyltin hydroxide and fentin acetate; Fludioxon il), fenpiclonil ) and their agriculturally acceptable acid addition salts.
  • fungicide compounds include tricyclazole, pyroquilon, carpropamide, diclocymet, fenoxanil, fthalide, fluazinam (f luazinam), cymoxanil, triforine (triforine), pyrifenox, fenarimol, fenpropidin, pencycuron, ferimzone, cyazofamid, iprovaricarb (i) provalicarb), benthiavalicarb isopropyl (benthiavalicarb) -isopropyl), iminoctadin albesilate, cyflufenamide, kasugamycin, validamycin, streptomycin , oxolinic acid, tebufloquin, isoprothiolane , tolprocarb, pydiflumetofen, picarbutrazox, mandestrobin, dipymethitrone, pyrazifl umi
  • Examples of the acaricides mentioned above include bromopropylate, tetradifon, propargite, amitraz, phenothiocarb, hexythiazox, fenbutatin oxide , dienochlor, fenpyroximate, tebufenpyrad, Pyridaben, pyrimidifen, clofentezine, etoxazole, halfenprox, milbemectin, acequinocyl inocyl), bifenazate, fluacrypyrim, spiro Examples include spirodichlorofen, spiromesifen, chlorfenapyr, avermectin, cyenopyrafen, and cyflumetofen.
  • the above herbicides include, for example, phenoxy acid compounds such as cyhalofop-butyl and 2,4-D; carbamate compounds such as esprocarb and desmedipham; Acid amide compounds such as alachlor and metolachlor; Urea compounds such as diuron and tebuthiuron; furon) etc.
  • Sulfonylurea compounds; pyrimidyloxybenzoic acid compounds such as pyriminobac-methyl; glufosinate salts (glufosinate) such as glyphosate, bilanafos, glufosinate, glufosinate ammonium Amino acid systems such as fosinate salt) Examples include compounds.
  • the plant disease control composition according to the present disclosure can also be applied after being mixed with a plant growth regulator or fertilizer. Moreover, the plant disease control composition of the present disclosure and the above-mentioned plant growth regulator or fertilizer can be applied separately at different times.
  • the above plant growth regulators include, for example, ethylene agents such as ethephon; auxin agents such as indolebutyric acid and ethychlozate; cytokinin agents; gibberellin agents; auxin antagonists; dwarfing agents; Examples include transpiration inhibitors.
  • the above-mentioned fertilizers include, for example, nitrogenous fertilizers such as urea, ammonium nitrate, ammonium nitrate, and ammonium chloride; Potassium fertilizers such as potassium chloride, potassium bicarbonate, potassium nitrate, potassium nitrate, potassium sodium nitrate; Manganese fertilizers such as manganese sulfate and manganese nitrate; Boron fertilizers such as boric acid and borates can be mentioned.
  • nitrogenous fertilizers such as urea, ammonium nitrate, ammonium nitrate, and ammonium chloride
  • Potassium fertilizers such as potassium chloride, potassium bicarbonate, potassium nitrate, potassium nitrate, potassium sodium nitrate
  • Manganese fertilizers such as manganese sulfate and manganese nitrate
  • Boron fertilizers such as boric acid and borates can be mentioned.
  • Wettable powder 2% by mass of tebufloquine, 20% by mass of probenazole, 58% by mass of clay, 2% by mass of white carbon, 13% by mass of diatomaceous earth, 4% by mass of calcium ligninsulfonate, 1% by mass of sodium lauryl sulfate. The mixture was uniformly mixed and ground to obtain a wettable powder.
  • (Formulation Example 2) Granule wettable powder Uniformly mixed and pulverized 2% by mass of tebufloquine, 20% by mass of isotianil, 68% by mass of clay, 5% by mass of dextrin, 4% by mass of alkylmaleic acid copolymer, and 1% by mass of sodium lauryl sulfate. After adding water and kneading well, the mixture was granulated and dried to obtain a granular wettable powder.
  • Test Example 1 Preventive spraying treatment against rice blast
  • the test solution was prepared by dissolving tebufloquine and each resistance inducer listed in Table 1 in acetone. This acetone solution was diluted with water to the concentration listed in Table 1, and 1/1,000 volume of a spreading agent (Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.) was added to form a spray solution. .
  • a spreading agent Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.
  • Control value ((number of lesions in untreated area - number of lesions in treated area) / number of lesions in untreated area) x 100
  • Test Example 2 Long-term control effect on rice blast
  • the test solution was prepared by dissolving tebufloquine and Compound A in acetone. This acetone solution was diluted with water to the concentration listed in Table 2, and 1/1,000 volume of a spreading agent (Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.) was added to form a spray solution. . 15 g of rice (variety: Jukoku) seeds were sown in a small vat measuring 30 cm x 20 cm, and cultivated in a greenhouse at 25° C./18° C. day and night.
  • a spreading agent Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.
  • conidia of rice blast fungus (Pyricularia oryzae) cultured on an agar medium were suspended at a concentration of 1 ⁇ 10 4 cells/mL to 5 ⁇ 10 4 cells/mL.
  • a solution obtained by diluting Tween 20 4000 times with deionized water was used for this suspension.
  • This rice blast conidia suspension was spray inoculated into two-leaf stage rice seedlings, and infected in a dark humid room for 24 hours. Thereafter, rice seedlings were cultivated in a greenhouse, and blast lesions were observed on the rice leaves 7 to 9 days after inoculation. 12 mL of the above spray solution was sprayed and air-dried indoors.
  • Control value ((number of lesions in untreated area - number of lesions in treated area) / number of lesions in untreated area) x 100
  • the plant disease control composition of the present disclosure has excellent control effects against rice blast, further reduces the risk of resistant bacteria, and is a useful composition for agricultural use.

Abstract

A plant disease control composition containing tebufloquin and an agent for inducing plant resistance as active ingredients.

Description

植物病害防除組成物、製剤及び植物病害防除方法Plant disease control compositions, formulations, and plant disease control methods
 本開示は、植物病害防除組成物、製剤及び植物病害防除方法に関する。 The present disclosure relates to a plant disease control composition, a formulation, and a plant disease control method.
 イネいもち病は、イネいもち病菌(Pyricularia oryzae)による水稲栽培において、もっとも被害の大きい病害であり、これまでに多くの殺菌化合物による防除剤が報告されている。 Rice blast is the most damaging disease in rice cultivation caused by the rice blast fungus (Pyricularia oryzae), and many control agents using fungicidal compounds have been reported so far.
 イネいもち病では既存の殺菌化合物に対する耐性菌が多数出現しており、1つの殺菌成分では十分な防除効果を得られない圃場が増えている(非特許文献1)。
 また、殺菌成分の一つであるテブフロキンを用いた組成物について開示されたものがあるものの(例えば、特許文献1~5)、テブフロキンと抵抗性誘導剤を併用する混合物については何ら示されていない。
In rice blast, many bacteria that are resistant to existing fungicidal compounds have appeared, and there are an increasing number of fields in which a single fungicidal component cannot provide sufficient control effects (Non-Patent Document 1).
Furthermore, although there are some disclosures about compositions using tebufloquine, which is one of the bactericidal ingredients (for example, Patent Documents 1 to 5), there is no disclosure whatsoever about a mixture using tebufloquine and a resistance inducer in combination. .
  特許文献1:特開2003-55114号公報
  特許文献2:国際公開第2004/039156号
  特許文献3:国際公開第2006/106811号
  特許文献4:特開2011-201858号公報
  特許文献5:特開2007-112760号公報
Patent Document 1: Japanese Patent Application Publication No. 2003-55114 Patent Document 2: International Publication No. 2004/039156 Patent Document 3: International Publication No. 2006/106811 Patent Document 4: Japanese Patent Application Publication No. 2011-201858 Patent Document 5: Japanese Patent Application Publication No. 2011-201858 Publication No. 2007-112760
  非特許文献1:薬剤耐性菌研究の最新動向と対策強化に向けて、日本農薬学会誌、第39号第1巻、53頁~57頁、2014年 Non-patent document 1: Latest trends in drug-resistant bacteria research and strengthening of countermeasures, Journal of the Japanese Society of Pesticides, No. 39, Volume 1, pp. 53-57, 2014
 上記に鑑み、複数の作用性を有する殺菌剤の需要が高まっている。
 また、更なる殺菌剤耐性菌の出現を予防する対策として、異なる作用性を有する物質を混合して植物病害を防除することが好ましいことが分かってきた。また、農薬による環境負荷低減の観点から、植物自身が持つ抵抗性を高めることで植物病害を防除する効果が高い抵抗性誘導剤を活用することが好ましいことも分かってきた。
In view of the above, there is an increasing demand for fungicides with multiple activities.
Furthermore, it has been found that as a measure to prevent further emergence of fungicide-resistant bacteria, it is preferable to mix substances with different activities to control plant diseases. Furthermore, from the perspective of reducing the environmental burden caused by pesticides, it has been found that it is preferable to utilize resistance inducers that are highly effective in controlling plant diseases by increasing the resistance that plants themselves have.
 本開示の一実施形態が解決しようとする課題は、テブフロキン単独を有効成分として含む植物病害防除組成物に比べて、植物病害に対する優れた防除効果を発揮し、併せて薬剤の施用量の低減、環境負荷の軽減を図る植物病害防除組成物を提供することにある。
 本開示の他の実施形態が解決しようとする課題は、植物病害防除組成物を用いた製剤及び植物病害防除方法を提供することにある。
The problem to be solved by an embodiment of the present disclosure is to exhibit an excellent control effect on plant diseases compared to a plant disease control composition containing tebufloquine alone as an active ingredient, and to reduce the amount of the drug applied. An object of the present invention is to provide a plant disease control composition that reduces environmental burden.
A problem to be solved by other embodiments of the present disclosure is to provide a formulation using a plant disease control composition and a method for controlling plant diseases.
 本発明者は、テブフロキンと植物抵抗性誘導剤が相乗的な植物病害防除効果を示すことを見出し、本発明を完成させた。
 すなわち、課題を解決するための具体的手段には、以下の態様が含まれる。
The present inventors have discovered that tebufloquine and a plant resistance inducer exhibit synergistic plant disease control effects, and have completed the present invention.
That is, specific means for solving the problem include the following aspects.
(1)テブフロキン及び植物抵抗性誘導剤を有効成分として含む植物病害防除組成物。
(2)植物病害が、いもち病害である(1)に記載の植物病害防除組成物。
(3)前記植物抵抗性誘導剤が、ジャスモン酸、サリチル酸、プロベナゾール、イソチアニル、チアジニル、アシベンゾラルS-メチル、ジクロベンチアゾクス、ラミナリン、オオイタドリ抽出物、バチルス・マイコイデス分離株J、サッカロミセス・セレビシアLAS117、ホセチル、亜リン酸又はその塩、及び下記の式(I)で表される化合物から選択される少なくとも1種を含む(1)に記載の植物病害防除組成物。
(1) A plant disease control composition containing tebufloquine and a plant resistance inducer as active ingredients.
(2) The plant disease control composition according to (1), wherein the plant disease is rice blast disease.
(3) The plant resistance inducer is jasmonic acid, salicylic acid, probenazole, isotianil, tiadinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, The plant disease control composition according to (1), comprising at least one selected from fosetyl, phosphorous acid or a salt thereof, and a compound represented by the following formula (I).
 式(I)中、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はトリフルオロメチル基を表し、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はメチル基を表し、Aはハロゲン原子、水酸基、アミノ基、メチルチオ基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキル基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキルオキシ基、炭素数1~4のアルキルカルボニル基、メトキシカルボニル基、エトキシカルボニル基、ベンジルアミノカルボニル基、アセトキシ基、ニトロ基、シアノ基、フェノキシ基及びベンジル基からなる群から選ばれる1個~5個の基で置換されていてもよいフェニル基を表し、Bは酸素原子又は硫黄原子を表し、Qは式:-NH-又は-O-で表される2価の基を表す。 In formula (I), X 1 and X 4 each independently represent a hydrogen atom, a fluorine atom, a chlorine atom, or a trifluoromethyl group, and X 2 and X 3 each independently represent a hydrogen atom, a fluorine atom, Represents a chlorine atom or a methyl group, A is a halogen atom, a hydroxyl group, an amino group, a methylthio group, an alkyl group having 1 to 4 carbon atoms optionally substituted with 1 to 3 halogen atoms, 1 to 3 Alkyloxy group having 1 to 4 carbon atoms which may be substituted with a halogen atom, alkylcarbonyl group having 1 to 4 carbon atoms, methoxycarbonyl group, ethoxycarbonyl group, benzylaminocarbonyl group, acetoxy group, nitro group, cyano group represents a phenyl group optionally substituted with 1 to 5 groups selected from the group consisting of a phenoxy group, a phenoxy group, and a benzyl group, B represents an oxygen atom or a sulfur atom, and Q represents the formula: -NH- or Represents a divalent group represented by -O-.
(4)(1)~(3)のいずれか1つに記載の植物病害防除組成物を含む製剤。
(5)水和剤、乳剤、フロアブル剤、顆粒水和剤、ドライフロアブル剤、粉剤、DL粉剤、FD粉剤、マイクロカプセル剤、粒剤、粉粒剤、ジャンボ粒剤、パック剤及びエアゾール剤から選択される(4)に記載の製剤。
(6)(1)~(3)のいずれか1つに記載の植物病害防除組成物を植物病害に施用する植物病害防除方法。
(7)前記植物病害が、いもち病害である(6)に記載の植物病害防除方法。
(8)前記施用が茎葉散布及び育苗箱処理の少なくとも一つの処理を含む(6)又は(7)に記載の植物病害防除方法。
(4) A formulation comprising the plant disease control composition according to any one of (1) to (3).
(5) From wettable powders, emulsions, flowables, hydrated granules, dry flowables, powders, DL powders, FD powders, microcapsules, granules, powder granules, jumbo granules, packs, and aerosols. The formulation according to (4) is selected.
(6) A method for controlling plant diseases, which comprises applying the plant disease control composition according to any one of (1) to (3) to plant diseases.
(7) The method for controlling a plant disease according to (6), wherein the plant disease is a rice blast disease.
(8) The method for controlling plant diseases according to (6) or (7), wherein the application includes at least one of foliage spraying and seedling box treatment.
 本開示の一実施形態によれば、テブフロキン単独を有効成分として含んでなる植物病害防除組成物に比べて、植物病害に対する優れた防除効果を発揮し、併せて薬剤の施用量の低減、環境負荷の軽減を図る植物病害防除組成物が提供される。
 本開示の他の実施形態によれば、植物病害防除組成物を用いた製剤及び植物病害防除方法が提供される。
According to an embodiment of the present disclosure, compared to a plant disease control composition containing tebufloquine alone as an active ingredient, it exhibits superior control effects against plant diseases, and also reduces the amount of application of the drug and causes environmental burden. Provided is a plant disease control composition that aims at alleviating.
According to other embodiments of the present disclosure, formulations and methods for controlling plant diseases using plant disease control compositions are provided.
 以下に、本開示の実施形態について説明する。なお、これらの説明及び実施例は本開示に係る実施形態を例示する目的で与えられるだけであり、本開示の範囲を制限するものではない。 Embodiments of the present disclosure will be described below. Note that these descriptions and examples are provided only for the purpose of illustrating the embodiments of the present disclosure, and do not limit the scope of the present disclosure.
 本明細書において、数値範囲を示す「~」とはその前後に記載される数値を下限値及び上限値として含む意味で使用される。 In this specification, "~" indicating a numerical range is used to include the numerical values written before and after it as the lower limit and upper limit.
 本明細書中に段階的に記載されている数値範囲において、一つの数値範囲で記載された
上限値又は下限値は、他の段階的な記載の数値範囲の上限値又は下限値に置き換えてもよい。また、本明細書中に記載されている数値範囲において、その数値範囲の上限値又は下限値は、実施例に示されている値に置き換えてもよい。
In the numerical ranges described step by step in this specification, the upper limit value or lower limit value described in one numerical range may be replaced with the upper limit value or lower limit value of another numerical range described step by step. good. Further, in the numerical ranges described in this specification, the upper limit or lower limit of the numerical range may be replaced with the value shown in the Examples.
 なお、本明細書において、対象物中の各成分の量は、対象物中に各成分に該当する物質が複数種存在する場合、特に断らない限り、対象物中に存在する当該複数種の物質の合計の含有率又は含有量を意味する。 In this specification, if there are multiple types of substances corresponding to each component in the target object, unless otherwise specified, the amount of each component in the target object is the amount of the multiple types of substances present in the target object. means the total content rate or amount of
 本開示の実施形態の一つは、テブフロキン及び植物抵抗性誘導剤を有効成分として含む植物病害防除組成物に関する。 One embodiment of the present disclosure relates to a plant disease control composition containing tebufloquine and a plant resistance inducer as active ingredients.
 ここでいう植物抵抗性誘導剤とは、植物病原菌に対し直接的な抗菌を示さない、あるいは抗菌的な作用を一部示すものの、その作用が防除を必要とする植物病原菌に対する主たる活性ではない物質をいう。さらに示せば、植物抵抗性誘導剤とは、殺菌剤耐性対策委員会(FRAC)でFRACコード表の作用機構P(宿主植物の抵抗性誘導)に分類される物質をいう。 Plant resistance inducers as used herein are substances that do not exhibit direct antibacterial activity against plant pathogens, or substances that exhibit some antibacterial activity but whose activity is not the main activity against plant pathogens that require control. means. More specifically, a plant resistance inducer refers to a substance classified by the Fungicide Resistance Control Committee (FRAC) as mode of action P (induction of host plant resistance) in the FRAC code table.
 本開示に係る植物病害防除組成物により効果が奏される機序は、必ずしも明らかではないが、以下のように推定される。
 本開示に係る植物病害防除組成物は、単独では植物病害に対して十分な防除効果が得られない殺菌剤を、異なる作用性を有する化合物と組み合わせて施用することで、殺菌作用と抵抗性誘導作用の相乗的な効果を有し、イネいもち病に代表される植物病害を効率的に防除でき、且つ、殺菌作用を持つ薬剤の散布回数を減らすことができる。また、本開示に係る植物病害防除組成物は、殺菌剤耐性菌出現リスクを低減できる。また、本開示に係る植物病害防除組成物は、一作期あたりの殺菌剤の施用量を減少させ、環境負荷を低減することもできる。
Although the mechanism by which the plant disease control composition according to the present disclosure exerts its effects is not necessarily clear, it is presumed as follows.
The plant disease control composition according to the present disclosure improves fungicidal action and induces resistance by applying a fungicide that does not have a sufficient control effect on plant diseases alone in combination with a compound having a different action. It has a synergistic effect, can efficiently control plant diseases such as rice blast, and can reduce the number of times of spraying of fungicidal agents. Moreover, the plant disease control composition according to the present disclosure can reduce the risk of emergence of fungicide-resistant bacteria. Furthermore, the plant disease control composition according to the present disclosure can reduce the amount of fungicide applied per cropping season, thereby reducing the environmental load.
 本開示に係る植物病害防除組成物は、農業生産の安定化、及び環境保護に大きな貢献をもたらすものである。 The plant disease control composition according to the present disclosure makes a significant contribution to stabilizing agricultural production and protecting the environment.
 本開示における植物抵抗性誘導剤としては、ジャスモン酸、サリチル酸、プロベナゾール、イソチアニル、チアジニル、アシベンゾラルS-メチル、ジクロベンチアゾクス、ラミナリン、オオイタドリ抽出物、バチルス・マイコイデス分離株J、サッカロミセス・セレビシアLAS117、ホセチル、亜リン酸及びその塩、及び、下記の式(I)で表される化合物が挙げられるが、これらに限定されるものではない。 The plant resistance inducers in the present disclosure include jasmonic acid, salicylic acid, probenazole, isotianil, tiadinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, Examples include, but are not limited to, fosetyl, phosphorous acid and its salts, and the compound represented by the following formula (I).
 式(I)中、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はトリフルオロメチル基を表し、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はメチル基を表し、Aはハロゲン原子、水酸基、アミノ基、メチルチオ基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキル基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキルオキシ基、炭素数1~4のアルキルカルボニル基、メトキシカルボニル基、エトキシカルボニル基、ベンジルアミノカルボニル基、アセトキシ基、ニトロ基、シアノ基、フェノキシ基及びベンジル基からなる群から選ばれる1個~5個の基で置換されていてもよいフェニル基を表し、Bは酸素原子又は硫黄原子を表し、Qは式:―NH―又は-O-で表される2価の基を表す。 In formula (I), X 1 and X 4 each independently represent a hydrogen atom, a fluorine atom, a chlorine atom, or a trifluoromethyl group, and X 2 and X 3 each independently represent a hydrogen atom, a fluorine atom, Represents a chlorine atom or a methyl group, A is a halogen atom, a hydroxyl group, an amino group, a methylthio group, an alkyl group having 1 to 4 carbon atoms optionally substituted with 1 to 3 halogen atoms, 1 to 3 Alkyloxy group having 1 to 4 carbon atoms which may be substituted with a halogen atom, alkylcarbonyl group having 1 to 4 carbon atoms, methoxycarbonyl group, ethoxycarbonyl group, benzylaminocarbonyl group, acetoxy group, nitro group, cyano group represents a phenyl group which may be substituted with 1 to 5 groups selected from the group consisting of a phenoxy group and a benzyl group, B represents an oxygen atom or a sulfur atom, and Q represents the formula: -NH- or Represents a divalent group represented by -O-.
 式(I)で表される化合物の具体例としては、2,6-difluoro-N-(3-methoxyphenyl)-4-Pyridinecarboxamide(CAS番号:2244744-34-9。以下、化合物Aともいう。)が挙げられる。 A specific example of the compound represented by formula (I) is 2,6-difluoro-N-(3-methoxyphenyl)-4-Pyridinecarboxamide (CAS number: 2244744-34-9. Hereinafter also referred to as compound A). can be mentioned.
 好ましい植物抵抗性誘導剤としては、プロベナゾール、イソチアニル、チアジニル、アシベンゾラルS-メチル、ジクロベンチアゾクス、ラミナリン、及び2,6-difluoro-N-(3-methoxyphenyl)-4-Pyridinecarboxamide(CAS番号:2244744-34-9)が挙げられる。 Preferred plant resistance inducers include probenazole, isotianil, thiazinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, and 2,6-difluoro-N-(3-methoxyphenyl)-4-pyridinecarboxamide (CAS number: 2244744). -34-9).
 本開示に係る植物病害防除組成物における、テブフロキンと植物抵抗性誘導剤の混合比率としては、以下の範囲が好ましい。
 テブフロキンと組み合わせる植物抵抗性誘導剤がプロベナゾール、イソチアニル、チアジニル、ジクロベンチアゾクス、アシベンゾラルS-メチル、又は式(I)で表される化合物の場合、質量比による混合比率は、テブフロキンが1に対して、組み合わせる植物抵抗性誘導剤が0.0001~10であることが好ましい。
 また、テブフロキンと組合せる植物抵抗性誘導剤がサリチル酸、ジャスモン酸、ラミナリン、オオイタドリ抽出物、バチルス・マイコイデス分離株J、サッカロミセス・セレビシアLAS117、ホセチル、又は亜リン酸もしくはその塩の場合、質量比による混合比率は、テブフロキンが1に対して、組み合わせる植物抵抗性誘導剤が0.0001~100であることが好ましい。
The mixing ratio of tebufloquine and plant resistance inducer in the plant disease control composition according to the present disclosure is preferably in the following range.
When the plant resistance inducer combined with tebufloquine is probenazole, isotianil, tiazinil, dichlorbenziazox, acibenzolar S-methyl, or a compound represented by formula (I), the mixing ratio by mass is 1:1:1: Therefore, it is preferable that the amount of the plant resistance inducer to be combined is 0.0001 to 10.
In addition, when the plant resistance inducer to be combined with tebufloquine is salicylic acid, jasmonic acid, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, fosetyl, or phosphorous acid or its salt, the mass ratio The mixing ratio is preferably 1:1 for tebufloquine and 0.0001 to 100:0 for the combined plant resistance inducer.
 より好ましくは、質量比による混合比率は、テブフロキンと組み合わせる植物抵抗性誘導剤がプロベナゾール、イソチアニル、チアジニル、ジクロベンチアゾクス、アシベンゾラルS-メチル、又は式(I)で表される化合物の場合、テブフロキンが1に対して、組み合わせる植物抵抗性誘導剤が0.01~10であり、テブフロキンと組み合わせる植物抵抗性誘導剤がラミナリンの場合、テブフロキンが1に対し、ラミナリンが0.1~10である。 More preferably, the mixing ratio by mass ratio is such that when the plant resistance inducer to be combined with tebufloquine is probenazole, isotianil, tiazinyl, dichlorbenziazox, acibenzolar S-methyl, or a compound represented by formula (I), tebufloquine is mixed with tebufloquine. is 1 to 0.01 to 10 for the combined plant resistance inducer, and when the plant resistance inducer to be combined with tebufloquine is laminarin, the ratio for tebufloquin is 1 to 0.1 to 10 for laminarin.
 本開示に係る植物病害防除組成物が防除の対象とする植物病原体としては、例えば、真菌、細菌、ウイルス等が挙げられる。但し、これらに限定されるものではない。
 真菌としては、例えば、植物病原真菌が挙げられ、細菌としては、例えば、植物病原細菌が挙げられ、ウイルスとしては、例えば、植物病原ウイルスが挙げられる。
Examples of plant pathogens to be controlled by the plant disease control composition according to the present disclosure include fungi, bacteria, viruses, and the like. However, it is not limited to these.
Examples of fungi include plant pathogenic fungi, examples of bacteria include plant pathogenic bacteria, and examples of viruses include plant pathogenic viruses.
 植物病原真菌としては、例えば、ナシ黒斑病菌(Alternaria alternata)、ナシ黒斑病菌(Alternaria kikutiana)、灰色かび病菌(Botrytis cinerea)、イネごま葉枯病菌(Cochliobolus
 miyabeanus)、ジャガイモ炭疽病菌(Colletotrichum atramentarium)、キュウリ炭疽病菌(Colletotrichum lagenarium)、キュウリつる割病菌(Fusarium oxysporum f.
 sp. cucumerinum)、トマト萎ちょう病菌(Fusarium oxysporum f. sp. lycopersici)、イネばか苗病菌(Gibberella fujikuroi)、ブドウ晩腐病菌(Glomerella cingulata)、イネいもち病菌(Pyricularia oryzae)、リゾクトニア苗立枯病菌(Rhizoctonia solani)、トマト小粒菌核病菌(Sclerotinia minor)、ジャガイモ半身萎ちょう病菌(Verticillium albo-atrum)、コムギ赤さび病菌(Puccinia recondi
ta)、オオムギうどんこ病菌(Erysiphe graminis)、ジャガイモ疫病菌(Phytophthora infestans)、キュウリべと病菌(Pseudoperonospora cubensis)、キュウリうどんこ病菌(Sphaerotheca fuliginea)、イネ苗立枯病菌(Pythium graminicola)、トマト輪紋病菌(Alternaria solani)、野菜類菌核病菌(Sclerotinia sclerotiorum)、リンゴ黒星病菌(Venturia inaequalis)、モモ灰星病菌(Monilinia fructicola)、イチゴ炭疸病菌(Colletotrichum gloeosporioides)、ダイズ紫斑病菌(Cercospora kikuchii)、テンサイ褐斑病菌(Cercospora beticola)、コムギふ枯病菌(Leptosphaeria nodorum)、コムギうどんこ病菌(Blumeria graminis)、イネ紋枯病菌(Thanatephorus cucumeris (Frank) Donk)が挙げられる。
Examples of plant pathogenic fungi include Alternaria alternata, Alternaria kikutiana, Botrytis cinerea, and Cochliobolus cinerea.
miyabeanus), potato anthracnose (Colletotrichum atramentarium), cucumber anthracnose (Colletotrichum lagenarium), cucumber vine splitting fungus (Fusarium oxysporum f.
sp. lycopersici, Gibberella fujikuroi, Glomerella cingulata, and Glomerella cingulata. Pyricularia oryzae, Rhizoctonia solani), Sclerotinia minor tomato, Verticillium albo-atrum, Puccinia recndi
ta), Erysiphe graminis, Phytophthora infestans, Pseudoperonospora cubensis, Sphaerotheca fuliginea), rice seedling damping-off fungus (Pythium graminicola), tomato ring Alternaria solani, Vegetable sclerotiorum, Venturia inaequalis, Monilinia fructicola, Strawberry anthracnose Colletotrichum gloeosporioides, soybean purpura (Cercospora kikuchii) , Cercospora beticola, Leptosphaeria nodorum, Blumeria graminis, Thanatephorus cucumeris (Fra nk) Donk).
 上記の植物病原真菌のうち、本開示に係る植物病害防除組成物が防除の対象として特に良好な効果が認められる好ましい植物病原真菌としては、イネごま葉枯病菌、イネばか苗病菌、イネいもち病菌、イネ苗立枯病菌、イネ紋枯病菌が挙げられ、より好ましい植物病原真菌としては、イネいもち病菌が挙げられる。 Among the above-mentioned plant pathogenic fungi, preferred plant pathogenic fungi for which the plant disease control composition according to the present disclosure has a particularly good effect as a control target include rice sesame leaf blight fungi, rice bakanae fungi, and rice blast fungi. , rice seedling blight disease fungi, and rice sheath blight disease fungi, and more preferred plant pathogenic fungi include rice blast fungi.
 また、植物病原細菌としては、例えば、Pseudomonas属、Erwinia属、Pectobacterium属、Xanthomonas属、Burkholderia属、Streptomyces属、Ralstonia属、Clavibacter属、Rhizomonas属、Agrobacterium属、Bacillus属、Clostridium属、Curtobacterium属、Pantoea属、Acidovorax属、Arthrobacter属、Rhodococcus属の細菌が挙げられる。 In addition, examples of plant pathogenic bacteria include Pseudomonas, Erwinia, Pectobacterium, Xanthomonas, Burkholderia, Streptomyces, Ralstonia, Clavibacter, and Rhizoma. nas genus, Agrobacterium genus, Bacillus genus, Clostridium genus, Curtobacterium genus, Pantoea Examples include bacteria of the genera Acidovorax, Arthrobacter, and Rhodococcus.
 さらに、植物病原ウイルスとしては、例えば、ムギ類萎縮ウイルス(Soil-borne wheatmosaic virus)、ダイズモザイクウイルス(Soybean mosaic virus)、アルファルファモザイクウイルス(Alfalfa mosaic virus)、ジャガイモ葉巻ウイルス(Potato leaf roll virus)、キュウリモザイクウイルス(Cucumber mosaic virus)、タバコモザイクウイルス(Tobacco mosaic virus)が挙げられる。 Furthermore, examples of plant pathogenic viruses include, for example, Soil-borne wheat mosaic virus, Soybean mosaic virus, Alfalfa mosaic virus, and Potato leaf curl virus. (Potato leaf roll virus), Examples include Cucumber mosaic virus and Tobacco mosaic virus.
 本開示に係る植物病害防除組成物を、製剤として用いる場合、本開示に係る植物病害防除組成物をそのまま用いてもよい。
 また、本開示に係る植物病害防除組成物を含む製剤を常法に従って任意の剤型にすることもできる。
When using the plant disease control composition according to the present disclosure as a formulation, the plant disease control composition according to the present disclosure may be used as is.
Further, a preparation containing the plant disease control composition according to the present disclosure can be made into any dosage form according to a conventional method.
 製剤の剤型としては、水和剤、乳剤、フロアブル剤、顆粒水和剤、ドライフロアブル剤、粉剤、DL粉剤、FD粉剤、又はマイクロカプセル剤などにすることができる。 The dosage form of the preparation may be a wettable powder, an emulsion, a flowable preparation, a granule wettable powder, a dry flowable preparation, a powder, a DL powder, an FD powder, or a microcapsule.
 製剤は、農薬として用いられる農薬用製剤であることが好ましい。 Preferably, the formulation is an agrochemical formulation used as an agrochemical.
 ここで、DL粉剤とは、飛散を抑制した製剤で、平均粒径が20μm以上で、粒径10μm以下の粒子が20%以下のものをいう。また、FD粉剤とは、飛散を利用した製剤で、平均粒径が5μm以下のものをいう。 Here, DL powder refers to a formulation that suppresses scattering and has an average particle size of 20 μm or more and 20% or less of particles with a particle size of 10 μm or less. Furthermore, FD powder is a formulation that utilizes scattering and has an average particle size of 5 μm or less.
 本開示に係る植物病害防疫組成物は、さらに、本田や育苗箱の水中に使用する粒剤、粉粒剤、ジャンボ粒剤、パック剤、エアゾール剤などの全ての製剤に用いることができる。 The plant disease prevention composition according to the present disclosure can further be used in all formulations such as granules, powders, jumbo granules, packs, and aerosols for use in water in Hondas and seedling boxes.
 これらの製剤は、必要に応じて農園芸学的に許容される添加剤を加えて製造することができる。
 農園芸学的に許容される添加剤としては、担体、界面活性剤、結合剤、増粘剤、凍結防止剤、着色剤、補助剤などが挙げられる。 
 担体としては、固体担体、液体担体、及びガス状担体が挙げられる。
 これらの添加剤とともに一般的な製造法で農薬用製剤を製造することができる。
These preparations can be manufactured by adding agriculturally and horticulturally acceptable additives, if necessary.
Agro-horticulturally acceptable additives include carriers, surfactants, binders, thickeners, antifreeze agents, colorants, adjuvants, and the like.
Carriers include solid carriers, liquid carriers, and gaseous carriers.
Agrochemical formulations can be produced together with these additives by common production methods.
 固体担体としては、例えば、粘土類(クレー、カリオン、珪藻土、ベントナイト、酸性白土など)、合成含水二酸化珪素、タルク、パーライト、バーミキュライト、軽石、その他の無機鉱物(セリサイト、石英、硫黄、活性炭、炭酸カルシウム、水和シリカ、酸化チタンなど)などの微粉末や粒状物、でんぷん、乳糖、塩化ビニル系重合体、ポリウレタンなどの合成ポリマー、木粉などの植物由来材料が挙げられる。 Examples of solid carriers include clays (clay, carrion, diatomaceous earth, bentonite, acid clay, etc.), synthetic hydrated silicon dioxide, talc, perlite, vermiculite, pumice, and other inorganic minerals (sericite, quartz, sulfur, activated carbon, Examples include fine powders and granules such as calcium carbonate, hydrated silica, titanium oxide, etc., synthetic polymers such as starch, lactose, vinyl chloride polymers, and polyurethane, and plant-derived materials such as wood flour.
 液体担体としては、例えば、アルコール類(メタノール、エタノール、イソプロパノール、ポリエチレングリコール、プロピレングリコール、ジプロピレングリコール、トリプロピレングリコール、グリセリンなど)、ケトン類(アセトン、メチルエチルケトンなど)、芳香族炭化水素類(ベンジルアルコール、ベンゼン、トルエン、キシレン、エチルベンゼン、メチルナフタレンなど)、脂肪族炭化水素類(パラフィン、n-ヘキサン、シク
ロヘキサン、ケロシン、灯油など)、エーテル類(ジエチレングリコールモノエチルエーテル、ジエチレングリコールモノメチルエーテル、ジイソプロピルエーテル、ジエチルエーテル、ジオキサン、テトラヒドロフランなど)、エステル類(炭酸プロピレン、酢酸エチル、酢酸ブチル、安息香酸ベンジル、ミリスチン酸イソプロピル、プロピレングリコールの脂肪酸エステルなど)、ニトリル類(アセトニトリル、イソブチロニトリルなど)、アミド類(ジメチルホルムアミド、ジメチルアセトアミド、N-メチルピロリドンなど)、ハロゲン化炭化水素類(ジクロロメタン、トリクロロエタン、四塩化炭素など)、ダイズ油、綿実油などの動植物油類、ジメチルスルホキシド、シリコーンオイル、高級脂肪酸、グリセロールホルマール、及び水などが挙げられる。
Examples of liquid carriers include alcohols (methanol, ethanol, isopropanol, polyethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, glycerin, etc.), ketones (acetone, methyl ethyl ketone, etc.), aromatic hydrocarbons (benzyl Alcohol, benzene, toluene, xylene, ethylbenzene, methylnaphthalene, etc.), aliphatic hydrocarbons (paraffin, n-hexane, cyclohexane, kerosene, kerosene, etc.), ethers (diethylene glycol monoethyl ether, diethylene glycol monomethyl ether, diisopropyl ether, diethyl ether, dioxane, tetrahydrofuran, etc.), esters (propylene carbonate, ethyl acetate, butyl acetate, benzyl benzoate, isopropyl myristate, propylene glycol fatty acid esters, etc.), nitriles (acetonitrile, isobutyronitrile, etc.), amides (dimethylformamide, dimethylacetamide, N-methylpyrrolidone, etc.), halogenated hydrocarbons (dichloromethane, trichloroethane, carbon tetrachloride, etc.), animal and vegetable oils such as soybean oil and cottonseed oil, dimethyl sulfoxide, silicone oil, higher fatty acids, Examples include glycerol formal and water.
 ガス状担体としてはLPG、空気、窒素、炭酸ガス、及びジメチルエーテルなどが挙げられる。 Examples of gaseous carriers include LPG, air, nitrogen, carbon dioxide, and dimethyl ether.
 本開示に係る植物病害防除組成物に用いられる担体の含有量は、通常、植物病害防組成物中に5質量%~99.9質量%であり、好ましくは、10質量%~98質量%である。 The content of the carrier used in the plant disease control composition according to the present disclosure is usually 5% by mass to 99.9% by mass, preferably 10% by mass to 98% by mass. be.
 界面活性剤は、乳化、分散、浸透、及び崩壊など様々な用途で用いられる。
 界面活性剤としては、非イオン性界面活性剤、及びアニオン性界面活性剤などを用いることができる。
Surfactants are used in a variety of applications, including emulsification, dispersion, penetration, and disintegration.
As the surfactant, nonionic surfactants, anionic surfactants, etc. can be used.
 非イオン性界面活性剤としては、ポリオキシエチレンアルキルエーテル類、ポリオキシエチレンスチリルフェニルエーテル類、ポリオキシエチレン・ポリオキシプロピレンブルックコポリマー類、(ポリオキシエチレン)ソルビタン脂肪酸エステル類などが用いられる。
 アニオン性界面活性剤としては、アルキル硫酸エステル類、アルキル(アリール)スルホン酸塩類、ナフタレンスルホン酸・ホルマリン縮合物類、リグニンスルホン酸塩、ポリカルボン酸塩類などが用いられる。
As the nonionic surfactant, polyoxyethylene alkyl ethers, polyoxyethylene styrylphenyl ethers, polyoxyethylene/polyoxypropylene Brook copolymers, (polyoxyethylene) sorbitan fatty acid esters, etc. are used.
As the anionic surfactant, alkyl sulfate esters, alkyl (aryl) sulfonates, naphthalene sulfonic acid/formalin condensates, lignin sulfonates, polycarboxylic acid salts, etc. are used.
 本開示に係る植物病害防除組成物に用いられる界面活性剤の量は、通常、植物病害防除組成物中に0.01質量%~30質量%であり、好ましくは、0.05質量%~20質量%である。 The amount of surfactant used in the plant disease control composition according to the present disclosure is usually 0.01% to 30% by mass, preferably 0.05% to 20% by mass. Mass%.
 結合剤としてはカルボキシメチルセルロース塩やメチルセルロースなどのセルロース系結合剤や、ポリビニルアルコール、アラビアゴム、デキストリンなどのデンプン系結合剤などが用いられる。
 増粘剤としては、キサンタンガムなどの有機ポリマー系増粘剤やベントナイトなどの無機系粉末などが用いられる。
 凍結防止剤としてはプロピレングリコールなどのグリコール系凍結防止剤などが用いられる。
 着色剤としては、例えば、青色1号や赤色2号等のタール色素、カラメル色素が用いられる。
 更に、製剤物性などを改良する目的として補助剤を加えることが出来る。例えば流動性を改良するためのホワイトカーボン、ステアリン酸カルシウム、防黴剤としてイソチアゾリン-3-オン誘導体などが用いられる。
As the binder, cellulose binders such as carboxymethyl cellulose salts and methyl cellulose, starch binders such as polyvinyl alcohol, gum arabic, and dextrin are used.
As the thickener, an organic polymer thickener such as xanthan gum or an inorganic powder such as bentonite is used.
As the anti-freezing agent, a glycol-based anti-freezing agent such as propylene glycol is used.
As the coloring agent, for example, tar dyes such as Blue No. 1 and Red No. 2, and caramel dyes are used.
Furthermore, adjuvants can be added for the purpose of improving the physical properties of the formulation. For example, white carbon, calcium stearate, and isothiazolin-3-one derivatives are used as fungicides to improve fluidity.
 本開示に係る植物病害防除組成物を含む製剤では、製剤中の含有量を限定するものではないが、製剤100質量部中、植物病害防除組成物を0.01質量部~90質量部の範囲から適宜その質量部を設定することができる。製剤中の植物病害防除組成物の好ましい含有量は、0.1質量部~50質量部の範囲である。 In the formulation containing the plant disease control composition according to the present disclosure, the content in the formulation is not limited, but the content of the plant disease control composition in 100 parts by mass of the formulation is in the range of 0.01 part by mass to 90 parts by mass. The mass part can be set appropriately from . The preferred content of the plant disease control composition in the formulation is in the range of 0.1 parts by mass to 50 parts by mass.
 本開示に係る植物病害防除組成物は、その施用量を限定するものではないが、例えば、植物病害防除の対象地域の天候、環境条件、栽培条件、生育状況、施用時期、施用方法、発病の程度などの発病因子により、適宜施用量を設定することが可能である。
 有効な植物病害防除組成物の施用量として、好ましくは10アールあたり0.01g~10kg、より好ましくは1g~5kgの範囲で施用することができる。
The plant disease control composition according to the present disclosure does not limit the application amount, but includes, for example, the weather, environmental conditions, cultivation conditions, growth conditions, application timing, application method, and disease onset of the target area for plant disease control. It is possible to appropriately set the application amount depending on disease-causing factors such as the severity of the disease.
The effective amount of the plant disease control composition to be applied is preferably 0.01 g to 10 kg, more preferably 1 g to 5 kg per 10 ares.
 本開示に係る植物病害防除組成物は、通常、農薬が使用されるすべての作物の栽培期間、すなわち、播種前から発芽期、育苗期、栄養成長期、収穫前までのいずれの時期においても用いることができる。
 本開示に係る植物病害防除組成物の好ましい使用法としては、イネの栽培期間において発芽後から育苗期、本田栽培、収穫前までのいずれの時期においても用いることができる。より好ましい使用法は育苗期から収穫前までである。
The plant disease control composition according to the present disclosure can be used during all crop cultivation periods in which pesticides are normally used, that is, from pre-sowing to germination, seedling-raising, vegetative growth, and pre-harvesting. be able to.
A preferred method of using the plant disease control composition according to the present disclosure is that it can be used at any time during the rice cultivation period, from after germination to the seedling-raising period, rice cultivation, and before harvest. A more preferred method of use is from the seedling-raising period to before harvest.
 本開示に係る植物病害防除組成物の施用としては、植物個体への茎葉散布処理、育苗箱処理、水稲田植機による側条施用、田面水への水面施用、土壌表面への散布処理、土壌表面への散布処理後の土壌混和、土壌中への注入処理、土壌中での注入処理後の土壌混和、土壌潅注処理、土壌潅注処理後の土壌混和、植物種子への吹き付け処理、植物種子への塗沫処理、植物種子の浸漬処理による施用、植物種子上の粉衣としての施用、植物種子との混合処理、肥料混和などが挙げられる。これらの施用により、植物病害を防除することができるが、より好ましい使用法は茎葉散布、育苗箱処理である。 Application of the plant disease control composition according to the present disclosure includes foliage spraying treatment on individual plants, seedling nursery box treatment, side row application using a paddy rice transplanter, water surface application to rice field water, spraying treatment on the soil surface, and soil surface treatment. Soil mixing after spraying, injection into the soil, soil mixing after injection into the soil, soil irrigation, soil mixing after soil irrigation, spraying onto plant seeds, mixing into plant seeds Examples include smearing, application by dipping plant seeds, application as a powder coating on plant seeds, mixing with plant seeds, and mixing with fertilizer. Plant diseases can be controlled by these applications, but more preferred methods of use are foliar spraying and seedling box treatment.
 本開示に係る植物病害防除組成物は、どのような施用においても植物病害防疫に対して十分な効力を発揮する。 The plant disease control composition according to the present disclosure exhibits sufficient efficacy for plant disease control in any application.
 本開示に係る植物病害防除組成物は、更に、殺虫剤、殺菌剤、殺ダニ剤、除草剤等の有害生物防除剤を混合して施用することもできる。
 また、本開示に係る植物病害防除組成物と上記の有害生物防除剤とを、別々に時間差を設けて施用することもできる。
The plant disease control composition according to the present disclosure can also be applied with a mixture of pest control agents such as insecticides, fungicides, acaricides, and herbicides.
Furthermore, the plant disease control composition according to the present disclosure and the pest control agent described above can be applied separately at different times.
 上記の殺虫剤としては、例えば、アセフェート(acephate)、ジクロルボス(dichlorvos)、EPN、フェニトロチオン(fenitrothion)、フ
ェナミホス(fenamifos)、プロチオホス(prothiofos)、プロフェノホス(profenofos)、ピラクロホス(pyraclofos)、クロルピリホスメチル(chlorpyrifos-methyl)、クロルフェンビンホス(chlorfenvinphos)、デメトン(demeton)、エチオン(ethion)、マラチオン(malathion)、クマホス(coumaphos)、イソキサチオン(isoxathion)、フェンチオン(fenthion)、ダイアジノン(diazinon)、チオジカルブ(thiodicarb)、アルジカルブ(aldicarb)、オキサミル(oxamyl)、プロポキスル(propoxur)、カルバリル(carbaryl)、フェノブカルブ(fenobucarb)、エチオフェンカルブ(ethiofencarb)、フェノチオカルブ(fenothiocarb)、ピリミカーブ(pirimicarb)、カルボフラン(carbofuran)、カルボスルファン(carbosulfan)、フラチオカルブ(furathiocarb)、ヒキンカルブ(hyquincarb)、アラニカルブ(alanycarb)、メソミル(methomyl)、ベンフラカルブ(benfuracarb)、カルタップ(cartap)、チオシクラム(thiocyclam)、ベンスルタップ(bensultap)、ジコホル(dicofol)、テトラジホン(tetradifon)、アクリナトリン(acrinathrin)、ビフェントリン(bifenthrin)、シクロプロトリン(cycloprothrin)、シフルトリン(cyfluthrin)、ジメフルトリン(dimefluthrin)、エンペントリン(empenthrin)、フェンフルトリン(fenfluthrin)、フェンプロパトリン(fenpropathrin)、イミプロトリン(imiprothrin)、メトフルトリン(metofluthrin)、ペルメトリン(permethrin)、フェノトリン(phenothrin)、レスメトリン(resmethrin)、テフルトリン(tefluthrin)、テトラメトリン(tetramethrin)、トラロメトリン(tralomethrin)、トランスフルトリン(transfluthrin)、シペルメトリン(cypermethrin)、デルタメトリン(deltamethrin)、シハロトリン(cyhalothrin)、フェンバレレート(fenvalerate)、フルバリネート(fluvalinate)、エトフェンプロックス(ethofenprox)、フルフェンプロックス(flufenprox)、ハルフェンプロックス(halfenprox)、シラフルオフェン(silafluofen)、シロマジン(cyromazine)、ジフルベンズロン(diflubenzuron)、テフルベンズロン(teflubenzuron)、フルシクロクスロン(flucycloxuron)、フルフェノクスロン(flufenoxuron)、ヘキサフルムロン(hexaflumuron)、ルフェヌロン(lufenuron)、ノバルロン(novaluron)、ペンフルロン(penfluron)、トリフルムロン(triflumuron)、クロルフルアズロン(chlorfluazuron)、ジアフェンチウロン(diafenthiuron)、メトプレン(methoprene)、フェノキシカルブ(fenoxycarb)、ピリプロキシフェン(pyriproxyfen)、ハロフェノジド(halofenozide)、テブフェノジド(tebufenozide)、メトキシフェノジド(methoxyfenozide)、クロマフェノジド(chromafenozide)、ジシクラニル(dicyclanil)、ブプロフェジン(buprofezin)、ヘキシチアゾクス(hexythiazox)、アミトラズ(amitraz)、クロルジメホルム(chlordimeform)、ピリダベン(pyridaben)、フェンピロキシメート(fenpyroxymate)、フルフェネリム(flufenerim)、ピリミジフェン(pyrimidifen)、テブフェンピラド(tebufenpyrad)、トルフェンピラド(tolfenpyrad)、フルアクリピリム(fluacrypyrim)、アセキノシル(acequinocyl)、シフルメトフェン(cyflumetofen)、フルベンジアミド(flubendiamide)、エチプロール(ethiprole)、フィプロニル(fipronil)、エトキサゾール(ethoxazole)、イミダクロ
プリド(imidacloprid)、ニテンピラム(nitenpyram)、クロチアニジン(c1othianidin)、アセタミプリド(acetamiprid)、ジノテフラン(dinotefuran)、チアクロプリド(thiacloprid)、チアメトキサム(thiamethoxam)、ピメトロジン(pymetrozine)、ビフェナゼート(bifenazate)、スピロジクロフェン(spirodiclofen)、スピロメシフェン(spiromesifen)、フロニカミド(flonicamid)、クロルフェナピル(chlorfenapyr)、ピリプロキシフェン(pyriproxyfene )、インドキサカルブ(indoxacarb)、ピリダリル(pyridalyl)、スピノサド(spinosad)、アベルメクチン(avermectin)、ミルベマイシン(milbemycin)、アザジラクチン(azadirachtin)、ニコチン(nicotine)、ロテノン(rotenone)、BT菌、BTタンパク質、昆虫病原ウイルス、エマメクチン安息香酸塩(emamectinbenzoate)、スピネトラム(spinetoram)、ピリフルキナゾン(pyrifluquinazon)、クロルアントラニリプロール(chlorantraniliprole)、シアントラニリプロール(cyantraniliprole)、シエノピラフェン(cyenopyrafen)、スピロテトラマット(spirotetramat)、レピメクチン(lepimectin)、メタフルミゾン(metaflumizone)、ピラフルプロール(pyrafluprole)、ピリプロール(pyriprole)、ジメフルスリン(dimefluthrin)、フェナザフロル(fenazaflor)、ヒドラメチルノン(hydramethylnon)、トリアザメート(triazamate)、アフィドピロペン(afidopyropen)、フルピリミン(flupyrimin)が挙げられる。
The above-mentioned insecticides include, for example, acephate, dichlorvos, EPN, fenitrothion, fenamifos, prothiofos, profenofos, pyraclofos. clofos), chlorpyrifos-methyl (chlorpyrifos) -methyl), chlorfenvinphos, demeton, ethion, malathion, coumaphos, isoxathion, fenthion, diazione diazinon, thiodicarb ), aldicarb, oxamyl, propoxur, carbaryl, fenobucarb, ethiofencarb, phenothiocarb, pirimicarb ( pirimicarb), carbofuran, carbosulfan (carbosulfan), furathiocarb, hyquincarb, alanycarb, methomyl, benfuracarb, cartap, thiocyc lam), bensultap, dicofol, tetradifon (tetradifon), acrinathrin, bifenthrin, cycloprothrin, cyfluthrin, dimefluthrin, empenthrin , fenfluthrin, fenpropathrin, imiprothrin, metofluthrin, permethrin, phenothrin, resmethrin, tefluthrin, tetramethrin rin), tralomethrin, transfluthrin, cypermethrin ( cypermethrin, deltamethrin, cyhalothrin, fenvalerate, fluvalinate, ethofenprox, flufenprox ), halfenprox, silafluofen , cyromazine, diflubenzuron, teflubenzuron, flucycloxuron, flufenoxuron, hexaflumuron uron), lufenuron, novaluron, penfluron ( penfluron, triflumuron, chlorfluazuron, diafenthiuron, methoprene, fenoxycarb, pyriproxyfen roxyfen), halofenozide, tebufenozide ), methoxyfenozide, chromafenozide, dicyclanil, buprofezin, hexythiazox, amitraz z), chlordimeform, pyridaben, fenpyroximate, flufenerim ), pyrimidifen, tebufenpyrad, tolfenpyrad, fluacrypyrim, acequinocyl, cyflumetofen, fulvene flubendiamide, ethiprole, fipronil, etoxazole ( ethoxazole), imidacloprid, nitenpyram, clothianidin, acetamiprid, dinotefuran, thiacloprid rid), thiamethoxam, pymetrozine, bifenazate, spirodiclo spirodiclofen, spiromesifen, flonicamid, chlorfenapyr, pyriproxyfene, indoxacarb, pyridalyl spinosad, avermectin , milbemycin, azadirachtin, nicotine, rotenone, BT bacterium, BT protein, entomopathogenic virus, emamectinbenzoate, spinetora m), pyrifluquinazone, chlor chlorantraniliprole, cyantraniliprole, cyenopyrafen, spirotetramat, lepimectin, metaflu mizone), pyrafluprole, pyriprole, Examples include dimefluthrin, fenazaflor, hydramethylnon, triazamate, afidopyropen, flupyrimin.
 上記の殺菌剤としては、例えば、アゾキシストロビン(azoxystrobin)、クレソキシムメチル(kresoxim-methyl)、トリフロキシストロビン(trifloxystrobin)、メトミノストロビン(metominostrobin)、オリサストロビン(orysastrobin)などのストロビルリン系化合物;メパニピリム(mepanipyrim)、ピリメサニル(pyrimethanil)、シプロジニル(cyprodinil)のようなアニリノピリミジン系化合物;トリアジメホン(triadimefon)、ビテルタノール(bitertanol)、トリフルミゾール(triflumizole)、メトコナゾール(metconazole)、プロピコナゾール(propiconazole)、ペンコナゾール(penconazole)、フルシラゾール(flusilazole)、ミクロブタニル(myclobutanil)、シプロコナゾール(cyproconazole)、テブコナゾール(tebuconazole)、ヘキサコナゾール(hexaconazole)、プロクロラズ(prochloraz)、シメコナゾール(simeconazole)のようなアゾール系化合物;キノメチオネート(chinomethionate)のようなキノキサリン系化合物;マンネブ(maneb)、ジネブ(zineb)、マンコゼブ(mancozeb)、ポリカーバメート(polycarbamate)、プロビネブ(propineb)のようなジチオカーバメート系化合物;ジエトフェンカルブ(diethofencarb)のようなフェニルカーバメート系化合物;クロロタロニル(chlorothalonil)、キントゼン(quintozene)のような有機塩素系化合物;ベノミル(benomyl)、チオファネートメチル(thiophanate-methyl)、カルベンダジム(carbendazim)のようなベンズイミダゾール系化合物;メタラキシル(metalaxyl)、オキサジキシル(oxadixyl)、オフラセ(ofurace)、ベナラキシル(benalaxyl)、フララキシル(furalaxyl)、シプロフラン(cyprofuram)のようなフェニルアミド系化合物;ジクロフルアニド(dichlofluanid)のようなスルフェン酸系化合物;水酸化第二銅(cupric hydroxide)、オキシキノリン銅(oxine-copper)のような銅系化合物;ヒドロキシイソキサゾール(hydroxyisoxazole)のようなイソキサゾール系化合物;ホセチルアルミニウム(fosetyl-aluminium)、トルクロホスメチル(tolclofos-methyl)のような有機リン系化合物;キャプタン(captan)、カプタホール(captafol)、フォルペット(folpet)のようなN-ハロアルキルチオ系化合物;プロシミドン(procymidone)、イプロジオン(iprodione)、ビンクロゾリン(vinclozolin)のようなジカルボキシイミド系化合物;フルトラニル(flutolanil)、メプロニル(mepronil)、フラメトピル(furametpyr)、チフルザミド(thifluzamide)、ボスカリド(boscalid)、ペンチオピラド(penthiopyrad)のようなカルボキシアニリド系化合物;フェンプロピモルフ(fenpropimorph)、ジメトモルフ(dimethomorph)のようなモルフォリン系化合物;水酸化トリフェニルスズ(fentin hydroxide)、酢酸トリフェニルスズ(fentin acetate)のような有機スズ系化合物;フルジオキソニル(fludioxonil)、フェンピクロニル(fenpiclonil)のようなシアノピロール系化合物及びこれらの農薬上許容可能な酸付加塩が挙げられる。 The above-mentioned fungicides include, for example, strobosides such as azoxystrobin, kresoxim-methyl, trifloxystrobin, metominostrobin, and orysastrobin. Bilurin compound; mepanipyrim Anilinopyrimidine compounds such as mepanipyrim, pyrimethanil, cyprodinil; triadimefon, bitertanol, triflumizole, meth Conazole (metconazole), propiconazole (propiconazole) , penconazole, flusilazole, myclobutanil, cyproconazole, tebuconazole, hexaconazole Azole compounds such as zole, prochloraz, and simeconazole ; quinoxaline compounds such as chinomethionate; dithiocarbamate compounds such as maneb, zineb, mancozeb, polycarbamate, propineb substance; diethofencarb phenyl carbamate compounds such as; organochlorine compounds such as chlorothalonil, quintozene; Benzimidazole compounds; metalaxyl Phenylamide compounds such as (metalaxyl), oxadixyl, ofurace, benalaxyl, furaxyl, cyprofuram; Sulfenic acid compounds such as; Copper-based compounds such as cupric hydroxide and oxyquinoline copper; isoxazole-based compounds such as hydroxyisoxazole; fosetyl-aluminum, tolclofos-methyl ( Organophosphorus compounds such as tolclofos-methyl; N-haloalkylthio compounds such as captan, captafol, and folpet; procymidone, iprodione, and vinclozolin. zolin ); dicarboximide compounds such as flutolanil, mepronil, furametpyr, thifluzamide, boscalid, penthiopyrad; Xyanilide compound; fenpropimorph Morpholine compounds such as (fenpropimorph) and dimethomorph; Organotin compounds such as triphenyltin hydroxide and fentin acetate; Fludioxon il), fenpiclonil ) and their agriculturally acceptable acid addition salts.
 さらに、その他の殺菌剤化合物として、トリシクラゾール(tricyclazole)、ピロキロン(pyroquilon)、カルプロパミド(carpropamid)、ジクロシメット(diclocymet)、フェノキサニル(fenoxanil)、フサライド(fthalide)、フルアジナム(fluazinam)、シモキサニル(cymoxanil)、トリホリン(triforine)、ピリフェノックス(pyrifenox)、フェナリモル(fenarimol)、フェンプロピディン(fenpropidin)、ペンシクロン(pencycuron)、フェリムゾン(ferimzone)、シアゾファミド(cyazofamid)、イプロバリカルブ(iprovalicarb)、ベンチアバリカルブイソプロピル(benthiavalicarb-isopropyl)、イミノクタジンアルベシル酸塩(iminoctadin albesilate)、シフルフェナミド(cyflufenamid)、カスガマイシン(kasugamycin)、バリダマイシン(validamycin)、ストレプトマイシン(streptomycin)、オキソリニック酸(oxolinic acid)、テブフロキン(tebufloquin)、イソプロチオラン(isoprothiolane)、トルプロカルブ(tolprocarb)、ピジフルメトフェン(pydiflumetofen)、ピカルブトラゾクス(picarbutrazox)、マンデストロビン(mandestrobin)、ジピメチトロン(dipymetitrone)、ピラジフルミド(pyraziflumid)、オキサチアピプロピリン(oxathiapiprolin)、ペンフルフェン(penflufen)、フルオキサピプロリン(fluoxapiprolin)、フロリルピコキサミド(florylpicoxamid)、フルオピモミド(fluopimomide)、イプフルフェノキン(ipflufenoquin)、フルインダピル(fluindapyr)、イソフルシプラム(isoflucypram)、キノフメリン(quinofumelin)、メチルテトラプロール(methyltetraprole)、ピリダクロメチル(pyridachlometyl)、ピラプロポイン(pyrapropoyne)、アミノピリフェン(aminopyrifen)、インピルフルキサム(inpyrfluxam)、及びこれらの農薬上許容可能な酸付加塩などが挙げられる。 Additionally, other fungicide compounds include tricyclazole, pyroquilon, carpropamide, diclocymet, fenoxanil, fthalide, fluazinam (f luazinam), cymoxanil, triforine (triforine), pyrifenox, fenarimol, fenpropidin, pencycuron, ferimzone, cyazofamid, iprovaricarb (i) provalicarb), benthiavalicarb isopropyl (benthiavalicarb) -isopropyl), iminoctadin albesilate, cyflufenamide, kasugamycin, validamycin, streptomycin , oxolinic acid, tebufloquin, isoprothiolane , tolprocarb, pydiflumetofen, picarbutrazox, mandestrobin, dipymethitrone, pyrazifl umid), oxathiapipropyline, penflufen ( penflufen), fluoxapiprolin, florylpicoxamide, fluopimomide, ipflufenoquin, fluindapyr , isoflucypram, quinofumelin, Examples include methyltetraprole, pyridachlomethyl, pyrapropoyne, aminopyrifen, inpyrfluxam, and agriculturally acceptable acid addition salts thereof.
 上記の殺ダニ剤としては、例えば、ブロモプロピレート(bromopropylate)、テトラジホン(tetradifon)、プロパルギット(propargite)、アミトラズ(amitraz)、フェノチオカルブ(fenothiocarb)、ヘキシチアゾクス(hexythiazox)、フェンブタチンオキシド(fenbutatin oxide)、ジエノクロル(dienochlor)、フェンピロキシメート(fenpyroximate)、テブフェンピラド(tebufenpyrad)、
ピリダベン(pyridaben)、ピリミジフェン(pyrimidifen)、クロフェンテジン(clofentezine)、エトキサゾール(etoxazole)、ハルフェンプロックス(halfenprox)、ミルベメクチン(milbemectin)、アセキノシル(acequinocyl)、ビフェナゼート(bifenazate)、フルアクリピリム(fluacrypyrim)、スピロジクロフェン(spirodichlofen)、スピロメシフェン(spiromesifen)、クロルフェナピル(chlorfenapyr)、アベルメクチン(Avermectin)、シエノピラフェン(cyenopyrafen)、シフルメトフェン(cyflumetofen)が挙げられる。
Examples of the acaricides mentioned above include bromopropylate, tetradifon, propargite, amitraz, phenothiocarb, hexythiazox, fenbutatin oxide , dienochlor, fenpyroximate, tebufenpyrad,
Pyridaben, pyrimidifen, clofentezine, etoxazole, halfenprox, milbemectin, acequinocyl inocyl), bifenazate, fluacrypyrim, spiro Examples include spirodichlorofen, spiromesifen, chlorfenapyr, avermectin, cyenopyrafen, and cyflumetofen.
 また、上記の除草剤としては、例えば、シハロホップブチル(cyhalofop-butyl)、2,4-D等のフェノキシ酸系化合物;エスプロカルブ(esprocarb)、デスメディファム(desmedipham)等のカーバメート系化合物;アラクロール(alachlor)、メトラクロール(metolachlor)等の酸アミド系化合物;ジウロン(diuron)、テブチウロン(tebuthiuron)等の尿素系化合物;ハロスルフロンメチル(halosulfuron-methyl)、フラザスルフロン(flazasulfuron)等のスルホニルウレア系化合物;ピリミノバックメチル(pyriminobac-methyl)等のピリミジルオキシ安息香酸系化合物;グリホサート(glyphosate)、ビアラホス(bilanafos)、グルホシネート(glufosinate)、グルホシネートアンモニウムなどのグルホシネート塩(glufosinate salt)等のアミノ酸系化合物が挙げられる。 In addition, the above herbicides include, for example, phenoxy acid compounds such as cyhalofop-butyl and 2,4-D; carbamate compounds such as esprocarb and desmedipham; Acid amide compounds such as alachlor and metolachlor; Urea compounds such as diuron and tebuthiuron; furon) etc. Sulfonylurea compounds; pyrimidyloxybenzoic acid compounds such as pyriminobac-methyl; glufosinate salts (glufosinate) such as glyphosate, bilanafos, glufosinate, glufosinate ammonium Amino acid systems such as fosinate salt) Examples include compounds.
 本開示に係る植物病害防除組成物は、植物成長調節剤や肥料と混合して施用することもできる。また、本開示の植物病害防除組成物と上記の植物成長調節剤や肥料とを、別々に時間差を設けて施用することもできる。 The plant disease control composition according to the present disclosure can also be applied after being mixed with a plant growth regulator or fertilizer. Moreover, the plant disease control composition of the present disclosure and the above-mentioned plant growth regulator or fertilizer can be applied separately at different times.
 上記の植物成長調節剤としては、例えば、エテホン(ethephon)等のエチレン剤;インドール酪酸(indolebutyric acid)、エチクロゼート(ethychlozate)等のオーキシン剤;サイトカイニン剤;ジベレリン剤;オーキシン拮抗剤;矮化剤;蒸散抑制剤が挙げられる。 The above plant growth regulators include, for example, ethylene agents such as ethephon; auxin agents such as indolebutyric acid and ethychlozate; cytokinin agents; gibberellin agents; auxin antagonists; dwarfing agents; Examples include transpiration inhibitors.
 また、上記の肥料としては、例えば、尿素、硝酸アンモニウム、硝酸苦土アンモニウム、塩化アンモニウム等の窒素質肥料;過リン酸石灰、リン酸アンモニウム、苦土過リン酸、苦土リン酸等のリン酸質肥料;塩化カリウム、重炭酸カリウム、硝酸カリ苦土、硝酸カリウム、硝酸カリナトリウム等のカリウム質肥料;硫酸マンガン、硝酸苦土マンガン等のマンガン質肥料;ホウ酸、ホウ酸塩等のホウ素質肥料が挙げられる。 In addition, the above-mentioned fertilizers include, for example, nitrogenous fertilizers such as urea, ammonium nitrate, ammonium nitrate, and ammonium chloride; Potassium fertilizers such as potassium chloride, potassium bicarbonate, potassium nitrate, potassium nitrate, potassium sodium nitrate; Manganese fertilizers such as manganese sulfate and manganese nitrate; Boron fertilizers such as boric acid and borates can be mentioned.
 以下、製剤例及び試験例を挙げて、本開示を具体的に説明するが、本開示はこれらの製剤例及び試験例に限定されるものではない。 Hereinafter, the present disclosure will be specifically explained with reference to formulation examples and test examples, but the present disclosure is not limited to these formulation examples and test examples.
(製剤例1)水和剤
 テブフロキン2質量%、プロベナゾール20質量%、クレー58質量%、ホワイトカーボン2質量%、ケイソウ土13質量%、リグニンスルホン酸カルシウム4質量%、ラウリル硫酸ナトリウム1質量%を均一に混合粉砕し、水和剤を得た。
(Formulation Example 1) Wettable powder: 2% by mass of tebufloquine, 20% by mass of probenazole, 58% by mass of clay, 2% by mass of white carbon, 13% by mass of diatomaceous earth, 4% by mass of calcium ligninsulfonate, 1% by mass of sodium lauryl sulfate. The mixture was uniformly mixed and ground to obtain a wettable powder.
(製剤例2)顆粒水和剤
 テブフロキン2質量%、イソチアニル20質量%、クレー68質量%、デキストリン5質量%、アルキルマレイン酸共重合物4質量%、ラウリル硫酸ナトリウム1質量%を均一に混合粉砕し、水を加えてよく練合した後、造粒乾燥して顆粒水和剤を得た。
(Formulation Example 2) Granule wettable powder Uniformly mixed and pulverized 2% by mass of tebufloquine, 20% by mass of isotianil, 68% by mass of clay, 5% by mass of dextrin, 4% by mass of alkylmaleic acid copolymer, and 1% by mass of sodium lauryl sulfate. After adding water and kneading well, the mixture was granulated and dried to obtain a granular wettable powder.
(製剤例3)フロアブル剤
 テブフロキン3質量%、ジクロベンチアゾクス30質量%、ポリオキシエチレンスチリルフェニルエーテル硫酸塩5質量%、プロピレングリコール6質量%、ベントナイト1質量%、シリコーン系消泡剤(商品名:PRONAL EX-300、東邦化学工業株式会社)0.05質量%、防黴剤(商品名:バイオホープL、ケイ・アイ化成株式会社)0.
02質量%を混合した後、適量の水を加え、湿式粉砕機にて粉砕した。その後、キサンタンガム1%水溶液3質量%及び残りの水を加えて100質量%とし、フロアブル剤を得た。
(Formulation Example 3) Flowable agent tebufloquine 3% by mass, diclobentiazox 30% by mass, polyoxyethylene styrylphenyl ether sulfate 5% by mass, propylene glycol 6% by mass, bentonite 1% by mass, silicone antifoaming agent (product Name: PRONAL EX-300, Toho Chemical Industry Co., Ltd.) 0.05% by mass, antifungal agent (Product name: Biohop L, K.I. Kasei Co., Ltd.) 0.
After mixing 0.02% by mass, an appropriate amount of water was added and the mixture was pulverized using a wet pulverizer. Thereafter, 3% by mass of a 1% xanthan gum aqueous solution and the remaining water were added to make 100% by mass to obtain a flowable agent.
(製剤例4)乳剤
 テブフロキン9.2質量%、2,6-ジフルオロ-N-(3-メトキシフェニル)-4-ピリジンカルボキサミド(化合物A)5.8質量%、N,N-ジメチルホルムアミド20質量%、芳香族系溶剤(商品名:T-SOL 150、ENEOS(株))55質量%、ポリオキシエチレンアルキルアリールエーテル10質量%を均一に混合して溶解し、乳剤を得た。
(Formulation Example 4) Emulsion 9.2% by mass of tebufloquine, 5.8% by mass of 2,6-difluoro-N-(3-methoxyphenyl)-4-pyridinecarboxamide (compound A), 20% by mass of N,N-dimethylformamide %, aromatic solvent (trade name: T-SOL 150, ENEOS Corporation), 55% by mass, and polyoxyethylene alkylaryl ether 10% by mass were uniformly mixed and dissolved to obtain an emulsion.
(製剤例5)ドライフロアブル剤
 テブフロキン10質量%、アシベンゾラルS-メチル10質量%、カオリンクレー65質量%、デキストリン5質量%、アルキルマレイン酸共重合物5質量%、ラウリル硫酸ナトリウム5質量%を均一に混合粉砕し、水を加えてよく練合した後、造粒乾燥してドライフロアブル剤を得た。
(Formulation example 5) Dry flowable agent 10% by mass of tebufloquine, 10% by mass of acibenzolar S-methyl, 65% by mass of kaolin clay, 5% by mass of dextrin, 5% by mass of alkylmaleic acid copolymer, 5% by mass of sodium lauryl sulfate uniformly After mixing and pulverizing the mixture, adding water and kneading well, the mixture was granulated and dried to obtain a dry flowable agent.
(製剤例6)粉剤
 テブフロキン0.5質量%、チアジニル5.0質量%、クレー57.5質量%、タルク36質量%、ステアリン酸カルシウム1質量%を均一に混合し、粉剤を得た。
(Formulation Example 6) Powder 0.5% by mass of tebufloquine, 5.0% by mass of tiadinil, 57.5% by mass of clay, 36% by mass of talc, and 1% by mass of calcium stearate were uniformly mixed to obtain a powder.
(製剤例7)DL粉剤
 テブフロキン1質量%、ラミナリン1質量%、DLクレー(商品名:昭和DLクレー、昭和KDE(株))95.5質量%、ホワイトカーボン2質量%、軽質流動パラフィン0.5質量%を均一に混合し、DL粉剤を得た。
(Formulation Example 7) DL powder Tebufloquine 1% by mass, laminarin 1% by mass, DL clay (trade name: Showa DL Clay, Showa KDE Co., Ltd.) 95.5% by mass, white carbon 2% by mass, light liquid paraffin 0. A DL powder was obtained by uniformly mixing 5% by mass.
(試験例1)イネいもち病に対する予防的散布処理
 試験溶液は、テブフロキン及び表1に記載の各抵抗性誘導剤をそれぞれアセトンで溶解した。このアセトン溶液を表1に記載の濃度となるように、水で希釈し、1/1,000容の展着剤(ネオエステリン、クミアイ化学工業(株)製)を加えて散布液とした。
(Test Example 1) Preventive spraying treatment against rice blast The test solution was prepared by dissolving tebufloquine and each resistance inducer listed in Table 1 in acetone. This acetone solution was diluted with water to the concentration listed in Table 1, and 1/1,000 volume of a spreading agent (Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.) was added to form a spray solution. .
 イネ(品種:十石)の種子8~10粒を直径3cmの小型ポットに植え、栽培土壌にて温室内で栽培した。2葉期又は3葉期の苗に上記のようにして調製した散布液を2mL散布し、自然乾燥した。 Eight to ten seeds of rice (variety: Jukoku) were planted in small pots with a diameter of 3 cm and cultivated in cultivation soil in a greenhouse. 2 mL of the spray solution prepared as described above was sprayed on seedlings at the 2-leaf or 3-leaf stage and allowed to air dry.
 一方、寒天培地上で培養したイネいもち病(Pyricularia oryzae)の分生子を1×10個/mL~5×10個/mLの濃度で懸濁した。この懸濁液にはTween20を脱イオン水で4000倍希釈した溶液を用いた。このイネいもち病分生子懸濁液をイネに噴霧接種し、湿室暗黒下で24時間感染させた。その後、イネを昼夜25℃/18℃の温室内で栽培し、接種から7日~9日後にイネ葉上に発病した、いもち病病斑数を基に下記の数式により防除価を算出した。そして、下記のコルビーの計算式を使って相乗効果の有無を検定した。 On the other hand, conidia of rice blast (Pyricularia oryzae) cultured on an agar medium were suspended at a concentration of 1 x 10 5 cells/mL to 5 x 10 5 cells/mL. For this suspension, a solution obtained by diluting Tween 20 4000 times with deionized water was used. This rice blast conidia suspension was spray inoculated into rice plants and infected in a dark humid room for 24 hours. Thereafter, rice was cultivated in a greenhouse at 25°C/18°C day and night, and the control value was calculated using the following formula based on the number of blast lesions that appeared on rice leaves 7 to 9 days after inoculation. Then, the presence or absence of a synergistic effect was tested using Colby's calculation formula below.
 防除価=((無処理区の病斑数-処理区の病斑数)/無処理区の病斑数)×100 Control value = ((number of lesions in untreated area - number of lesions in treated area) / number of lesions in untreated area) x 100
(コルビーの計算式)
 理論値=(防除価A+防除価B)-(防除価A×防除価B)/100
(Colby calculation formula)
Theoretical value = (Preventive value A + Preventive value B) - (Preventive value A × Preventive value B) / 100
 以下に示した表1の結果では、実際の防除価がコルビーの理論値を上回り、相乗効果を示すことが確認された。 The results shown in Table 1 below show that the actual control value exceeds Colby's theoretical value, demonstrating a synergistic effect.
Figure JPOXMLDOC01-appb-T000004
Figure JPOXMLDOC01-appb-T000004
(試験例2)イネいもち病に対する長期防除効果
 試験溶液は、テブフロキン及び化合物Aをそれぞれアセトンに溶解した。このアセトン溶液を表2に記載の濃度となるように、水で希釈し、1/1,000容の展着剤(ネオエステリン、クミアイ化学工業(株)製)を加えて散布液とした。
 イネ(品種:十石)の種子は30cm×20cmの小型バットに15gを播種し、昼夜25℃/18℃の温室内で栽培した。
(Test Example 2) Long-term control effect on rice blast The test solution was prepared by dissolving tebufloquine and Compound A in acetone. This acetone solution was diluted with water to the concentration listed in Table 2, and 1/1,000 volume of a spreading agent (Neoesterin, manufactured by Kumiai Chemical Industry Co., Ltd.) was added to form a spray solution. .
15 g of rice (variety: Jukoku) seeds were sown in a small vat measuring 30 cm x 20 cm, and cultivated in a greenhouse at 25° C./18° C. day and night.
 一方、寒天培地上で培養したイネいもち病菌(Pyricularia oryzae)の分生子を1×10個/mL~5×10個/mLの濃度で懸濁した。この懸濁液にはTween20を脱イオン水で4000倍希釈した溶液を用いた。このいもち病分生子懸濁液を2葉期のイネの苗に噴霧接種し、湿室暗黒下で24時間感染させた。その後はイネの苗を温室内で栽培し、接種から7日~9日後にイネ葉上にいもち病斑を確認した。
 上記の散布液を12mL散布し、室内にて自然乾燥させた。その後、湿室(温度25℃、湿度100%)に24時間静置し、バット内でいもち病菌を自然感染させた。
 さらに1週間後、同様に24時間自然感染させた。その後、昼夜25℃/18℃に設定
した温室内にてイネの苗を7日~9日間栽培し、無作為に抽出した50苗の展開済みの最上位葉に形成されたイネいもち病の病斑数を計測した。得られた病斑数を基に下記の数式により防除価を算出した。そして、コルビーの計算式を使って相乗効果の有無を検定した。
On the other hand, conidia of rice blast fungus (Pyricularia oryzae) cultured on an agar medium were suspended at a concentration of 1×10 4 cells/mL to 5×10 4 cells/mL. For this suspension, a solution obtained by diluting Tween 20 4000 times with deionized water was used. This rice blast conidia suspension was spray inoculated into two-leaf stage rice seedlings, and infected in a dark humid room for 24 hours. Thereafter, rice seedlings were cultivated in a greenhouse, and blast lesions were observed on the rice leaves 7 to 9 days after inoculation.
12 mL of the above spray solution was sprayed and air-dried indoors. Thereafter, it was left in a wet room (temperature: 25°C, humidity: 100%) for 24 hours, and the rice blast fungus was naturally infected in the vat.
After another week, the cells were naturally infected for 24 hours. After that, rice seedlings were cultivated for 7 to 9 days in a greenhouse set at 25°C/18°C during the day and night, and rice blast disease formed on the expanded uppermost leaves of 50 randomly selected seedlings. The number of spots was measured. Based on the number of lesions obtained, the control value was calculated using the following formula. Then, the presence or absence of a synergistic effect was tested using Colby's formula.
 防除価=((無処理区の病斑数-処理区の病斑数)/無処理区の病斑数)×100 Control value = ((number of lesions in untreated area - number of lesions in treated area) / number of lesions in untreated area) x 100
(コルビーの理論式)
 理論値 =(防除価A+防除価B)-(防除価A×防除価B)/100
(Colby's theoretical formula)
Theoretical value = (Preventive value A + Preventive value B) - (Preventive value A × Preventive value B) / 100
 以下に示した表2の結果では、実際の防除価がコルビーの理論値を大きく上回り、相乗効果を示すことが確認された。 The results shown in Table 2 below show that the actual control value greatly exceeds Colby's theoretical value, confirming a synergistic effect.
Figure JPOXMLDOC01-appb-T000005
Figure JPOXMLDOC01-appb-T000005
 本開示の植物病害防除組成物は、イネいもち病に対してその防除効果に優れ、さらには耐性菌リスクを低減し、農業用として有用な組成物である。 The plant disease control composition of the present disclosure has excellent control effects against rice blast, further reduces the risk of resistant bacteria, and is a useful composition for agricultural use.
 2022年3月28日に出願された日本国特許出願2022-052593号の開示は、その全体が参照により本明細書に取り込まれる。また、本明細書に記載された全ての文献、特許出願、及び技術規格は、個々の文献、特許出願、及び技術規格が参照により取り込まれることが具体的かつ個々に記された場合と同程度に、本明細書中に参照により取り込まれる。 The disclosure of Japanese Patent Application No. 2022-052593 filed on March 28, 2022 is incorporated herein by reference in its entirety. In addition, all documents, patent applications, and technical standards mentioned herein are incorporated by reference to the same extent as if each individual document, patent application, and technical standard were specifically and individually indicated to be incorporated by reference. , herein incorporated by reference.

Claims (8)

  1.  テブフロキン及び植物抵抗性誘導剤を有効成分として含む植物病害防除組成物。 A plant disease control composition containing tebufloquine and a plant resistance inducer as active ingredients.
  2.  植物病害が、いもち病害である請求項1に記載の植物病害防除組成物。 The plant disease control composition according to claim 1, wherein the plant disease is blast disease.
  3.  前記植物抵抗性誘導剤が、ジャスモン酸、サリチル酸、プロベナゾール、イソチアニル、チアジニル、アシベンゾラルS-メチル、ジクロベンチアゾクス、ラミナリン、オオイタドリ抽出物、バチルス・マイコイデス分離株J、サッカロミセス・セレビシアLAS117、ホセチル、亜リン酸又はその塩、及び下記の式(I)で表される化合物から選択される少なくとも1種を含む請求項1に記載の植物病害防除組成物。

     
     [式(I)中、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はトリフルオロメチル基を表し、X及びXは、それぞれ独立に、水素原子、フッ素原子、塩素原子又はメチル基を表し、Aはハロゲン原子、水酸基、アミノ基、メチルチオ基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキル基、1個~3個のハロゲン原子により置換されていてもよい炭素数1~4のアルキルオキシ基、炭素数1~4のアルキルカルボニル基、メトキシカルボニル基、エトキシカルボニル基、ベンジルアミノカルボニル基、アセトキシ基、ニトロ基、シアノ基、フェノキシ基及びベンジル基からなる群から選ばれる1個~5個の基で置換されていてもよいフェニル基を表し、Bは酸素原子又は硫黄原子を表し、Qは式:-NH-又は-O-で表される2価の基を表す。]
    The plant resistance inducers include jasmonic acid, salicylic acid, probenazole, isotianil, thiazinyl, acibenzolar S-methyl, dichlorbenziazox, laminarin, Japanese knotweed extract, Bacillus mycoides isolate J, Saccharomyces cerevisiae LAS117, fosetyl, The plant disease control composition according to claim 1, comprising at least one selected from phosphoric acid or a salt thereof and a compound represented by the following formula (I).


    [In formula (I), X 1 and X 4 each independently represent a hydrogen atom, a fluorine atom, a chlorine atom, or a trifluoromethyl group, and X 2 and X 3 each independently represent a hydrogen atom, a fluorine atom , represents a chlorine atom or a methyl group, A is a halogen atom, a hydroxyl group, an amino group, a methylthio group, an alkyl group having 1 to 4 carbon atoms optionally substituted with 1 to 3 halogen atoms, 1 to 3 an alkyloxy group having 1 to 4 carbon atoms which may be substituted with halogen atoms, an alkylcarbonyl group having 1 to 4 carbon atoms, a methoxycarbonyl group, an ethoxycarbonyl group, a benzylaminocarbonyl group, an acetoxy group, a nitro group, Represents a phenyl group optionally substituted with 1 to 5 groups selected from the group consisting of a cyano group, a phenoxy group, and a benzyl group, B represents an oxygen atom or a sulfur atom, and Q has the formula: -NH- Or represents a divalent group represented by -O-. ]
  4.  請求項1~請求項3のいずれか1項に記載の植物病害防除組成物を含む製剤。 A preparation comprising the plant disease control composition according to any one of claims 1 to 3.
  5.  水和剤、乳剤、フロアブル剤、顆粒水和剤、ドライフロアブル剤、粉剤、DL粉剤、FD粉剤、マイクロカプセル剤、粒剤、粉粒剤、ジャンボ粒剤、パック剤及びエアゾール剤から選択される請求項4に記載の製剤。 Selected from wettable powders, emulsions, flowables, wettable powders, dry flowables, powders, DL powders, FD powders, microcapsules, granules, powder granules, jumbo granules, packs, and aerosols. The formulation according to claim 4.
  6.  請求項1~請求項3のいずれか1項に記載の植物病害防除組成物を植物病害に施用する植物病害防除方法。 A method for controlling plant diseases, which comprises applying the plant disease control composition according to any one of claims 1 to 3 to plant diseases.
  7.  前記植物病害が、いもち病害である請求項6に記載の植物病害防除方法。 The method for controlling a plant disease according to claim 6, wherein the plant disease is a rice blast disease.
  8.  前記施用が、茎葉散布及び育苗箱処理の少なくとも一つの処理を含む請求項6又は請求項7に記載の植物病害防除方法。 The method for controlling plant diseases according to claim 6 or 7, wherein the application includes at least one of foliage spraying and seedling box treatment.
PCT/JP2023/010760 2022-03-28 2023-03-17 Plant disease control composition, preparation, and plant disease control method WO2023189782A1 (en)

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* Cited by examiner, † Cited by third party
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WO2018178878A1 (en) * 2017-03-31 2018-10-04 Bayer Healthcare Llc Biometric authentication for, and secure electronic tracking of, restricted over-the-counter drug sales
WO2020050297A1 (en) * 2018-09-06 2020-03-12 Meiji Seikaファルマ株式会社 Plant disease control agent

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2018178878A1 (en) * 2017-03-31 2018-10-04 Bayer Healthcare Llc Biometric authentication for, and secure electronic tracking of, restricted over-the-counter drug sales
WO2020050297A1 (en) * 2018-09-06 2020-03-12 Meiji Seikaファルマ株式会社 Plant disease control agent

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
YAMAMOTO, KENTARO. MATSUMURA, MAKOTO: "(4) Rice blast fungus -Tebufloquin-", PLANT PROTECTION, vol. 70, no. 8, 2016, XP093093821 *

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