WO2011108123A2 - Composition et procédé de lutte contre des nuisibles - Google Patents

Composition et procédé de lutte contre des nuisibles Download PDF

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Publication number
WO2011108123A2
WO2011108123A2 PCT/JP2010/056282 JP2010056282W WO2011108123A2 WO 2011108123 A2 WO2011108123 A2 WO 2011108123A2 JP 2010056282 W JP2010056282 W JP 2010056282W WO 2011108123 A2 WO2011108123 A2 WO 2011108123A2
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Prior art keywords
parts
pests
seeds
formulation
pest
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PCT/JP2010/056282
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English (en)
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WO2011108123A3 (fr
Inventor
Soichi Tanaka
Mayuko Ozawa
So Kiguchi
Atsushi Iwata
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Sumitomo Chemical Company, Limited
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Publication of WO2011108123A2 publication Critical patent/WO2011108123A2/fr
Publication of WO2011108123A3 publication Critical patent/WO2011108123A3/fr

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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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/44Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
    • A01N37/46N-acyl derivatives
    • 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • A01N37/38Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
    • 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
    • A01N43/74Biocides, 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
    • A01N43/781,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • 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
    • A01N51/00Biocides, 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
    • 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
    • A01N57/00Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
    • A01N57/10Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds
    • A01N57/14Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing aromatic radicals

Definitions

  • the present invention relates to a pest controlling composition and a method for controlling pests.
  • An object of the present invention is to provide a pest controlling composition having an excellent control effect against pests.
  • the present inventors have studied so as to find a pest controlling composition having an excellent control effect against pests and found that a pest controlling composition containing clothianidin, tolclophos-methyl , metalaxyl and a compound represented by formula (1) :
  • the present invention provides [1] to [9] shown below:
  • Group (A) consisting of:
  • metconazole metconazole, tebuconazole, difenoconazole, triticonazole, imazalil, triadimenol, fluquinconazole, prochloraz, prothioconazole, diniconazole, diniconazole- , ipconazole, cyproconazole, tetraconazole, carboxin, oxycarboxin, fludioxonil, thiuram, captan, thiophanate-methyl and thiabendazole;
  • a method for controlling pests which includes the step of applying an effective amount of the pest controlling composition according to any one of [1] to [4] to pests or habitats of the pests;
  • a method for controlling pests which includes the step of applying an effective amount of the pest controlling composition according to any one of [1] to [4] to plant seeds ;
  • Pests can be controlled by the present invention
  • the pest controlling composition of the present invention contains clothianidin, tolclophos-methyl, metalaxyl and a compound represented by formula (1) :
  • clothianidin, tolclophos-methyl and metalaxyl used in the present invention are known compounds and are described, for example, in "THE PESTICIDE MANUAL - 15th EDITION (published by BCPC) ISBN 1901396188", page 229, page 1135 and page 737. These compounds are obtained from commercially available formulations or obtained by
  • the present compound (1) used in the present invention (hereinafter referred to as the present compound (1)) is a compound described, for example, in Internal Publication No. WO 95/27693 pamphlet and Internal Publication No. WO 02/10101 pamphlet, and can be synthesized by the methods described, for example, in the pamphlets.
  • composition of the present invention the total content of tolclophos-methyl, metalaxyl and the present compound (1) is usually from 2 to 10,000,000 parts by weight, and
  • the pest controlling composition of the present invention can contain, in addition to clothianidin, tolclophos-methyl, metalaxyl and the present compound (1) , compound (s) selected from the following Group (A):
  • Group (A) consisting of:
  • metconazole metconazole, tebuconazole, difenoconazole, triticonazole, imazalil, triadimenol, fluquinconazole, prochloraz,
  • prothioconazole diniconazole, diniconazole-M, ipconazole, cyproconazole, tetraconazole, carboxin, oxycarboxin, fludioxonil, thiuram, captan, thiophanate-methyl and thiabendazole.
  • metconazole tebuconazole, difenoconazole, triticonazole, imazalil, triadimenol, fluquinconazole, prochloraz, prothioconazole, diniconazole, diniconazole-M, ipconazole, cyproconazole, tetraconazole, carboxin, oxycarboxin, fludioxonil, thiuram, captan, thiophanate- methyl and thiabendazole are known compounds and are described, for example, in "THE PESTICIDE MANUAL - 15th EDITION (published by BCPC) ISBN 1901396188", page 749, page 1072, page 354, page 1182, page 629, page 1147, page 543, page 928, page 965, page 384, page 663, page 287, page 1096, page 164, page 855, page 520, page 1132, page 154, page 1128
  • the content thereof is not particularly limited and is usually from 2 to 10,000,000 parts by weight, and preferably from 5 to 50,000 parts by weight, based on 1,000 parts by weight of clothianidin .
  • the pest controlling composition of the present invention may be produced by merely mixing clothianidin, tolclophos-methyl, metalaxyl and the present compound (1), and optional compound (s) selected from Group (A), but is usually produced by mixing these compounds with an inert carrier, optionally adding surfactants and other adjuvants for formulation, and formulating the resultant mixture into oil solutions, emulsifiable concentrates, flowable
  • the pest controlling composition can be used as a pest control agent as it is, or after adding other inert ingredients.
  • the total content of clothianidin, tolclophos-methyl, metalaxyl and the present compound (1) , and optional compound (s) selected from Group (A) in the pest controlling composition of the present invention is usually within a range from 0.1 to 99% by weight, preferably from 0.2 to 90% by weight, and more preferably from 1 to 80% by weight.
  • insecticides or fungicides other than those described above may be optionally added.
  • insecticides or fungicides ethaboxam is preferably exemplified.
  • solid carrier used in the formulation examples include fine powers and granules of minerals such as kaolin clay, attapulgite clay, bentonite, montmorillonite, acid clay, pyrophyllite, talc, diatomite, and calcite; natural organic substances such as corncob powder and walnut shell powder; synthetic organic substances such as urea; salts such as calcium carbonate and ammonium sulfate; and
  • liquid carrier examples include aromatic hydrocarbons such as xylene, alkylbenzene, AND methylnaphthalene; alcohols such as 2-propanol, ethylene glycol, propylene glycol, and ethylene glycol monoethyl ether; ketones such as acetone, cyclohexanone, and
  • isophorone vegetable oils such as soybean oil and
  • esters dimethylsulfoxide; acetonitrile and water.
  • surfactant examples include anionic
  • surfactants such as alkylsulfuric acid ester salt,
  • alkylarylsulfonic acid salt dialkylsulfosuccinic acid salt, polyoxyethylenealkylaryletherphosphoric acid ester salt, lignin sulfonic acid salt, and naphthalenesulfonate
  • nonionic surfactants such as polyoxyethylene alkyl aryl ether, polyoxyethylene- alkylpolyoxypropylene block copolymer, and sorbitan fatty acid ester; and cationic surfactants such as
  • alkyltrimethylammonium salt alkyltrimethylammonium salt.
  • the other adjuvants for formulation include water-soluble polymers such as polyvinyl alcohol and polyvinyl pyrrolidone; gum arable; alginic acid and salts thereof; polysaccharides such as CMC (carboxymethyl cellulose) and xanthan gum; inorganic substances such as aluminum magnesium silicate and alumina sol; preservatives; colorants; and stabilizing agents such as PAP (isopropyl acidic phosphate) and BH .
  • water-soluble polymers such as polyvinyl alcohol and polyvinyl pyrrolidone
  • gum arable alginic acid and salts thereof
  • polysaccharides such as CMC (carboxymethyl cellulose) and xanthan gum
  • inorganic substances such as aluminum magnesium silicate and alumina sol
  • preservatives colorants
  • stabilizing agents such as PAP (isopropyl acidic phosphate) and BH .
  • the pest controlling composition of the present invention can be used so as to protect plants from
  • infestation due to pests for example, noxious arthropods such as noxious insects and noxious mites, and plant diseases
  • pests for example, noxious arthropods such as noxious insects and noxious mites, and plant diseases
  • noxious arthropods such as noxious insects and noxious mites, and plant diseases
  • infestation such as feeding or
  • Hemiptera pests planthoppers such as Laodelphax striatellus, Nilaparvata lugens, and Sogatella furcifera, leafhoppers such as Nephotettix cincticeps and Nephotettix virescens, aphids such as Aphis gossypii, Myzus persicae, Brevicoryne brassicae, Macrosiphum euphorbiae, Aulacorthum solani, Rhopalosiphum padi, and Toxoptera citricidus, plant bugs such as Nezara antennata, Riptortus clavetus,
  • Leptocorisa chinensis Leptocorisa chinensis, Eysarcoris parvus, Halyomorpha mista, and Lyus lineolaris, whiteflies such as Trialeurodes
  • Lepidoptera pests Pyralidae such as Chilo
  • Adoxophyes sp. Homona magnanima, Archips fuscocupreanus, and Cydia pomonella
  • Gracillariidae such as Caloptilia theivora
  • Phyllonorycter ringoneella Carposinidae such as Carposina niponensis, Lyonetiidae such as Lyonetia spp., Lymantriidae such as Lymantria spp.
  • Yponameutidae such as Plutella xylostella
  • Gelechiidae such as Pectinophora gossypiella and Phthorimaea operculella
  • Arctiidae such as Hyphantria cunea
  • Tineidae such as Tinea translucens
  • Thysanoptera pests Thripidae such as Frankliniella occidentalis, Thrips peri, Scirtothrips dorsalis, Thrips tabaci, Frankliniella intonsa, and Frankliniella fusca;
  • Diptera pests Agromyzidae such as Hylemya antiqua, Hylemya platura, Agromyza oryzae, Hydrellia griseola,
  • Chlorops oryzae and Liriomyza trifolii, Dacus cucurbitae, and Ceratitis capitata;
  • Coleoptera pests Epilachna vigintioctopunctata
  • Aulacophora femoralis Phyllotreta striolata, Oulema oryzae, Echinocnemus squameus, Lissorhoptrus oryzophilus,
  • Anthonomus grandis Callosobruchus chinensis, Sphenophorus venatus, Popillia japonica, Anomala cuprea, Diabrotica spp., Leptinotarsa decemlineata, Agriotes spp., and Lasioderma serricorne;
  • Orthoptera pests Gryllotalpa africana, Oxya
  • Hymenoptera pests Athalia rosae, Acromyrmex spp., and Solenopsis spp..
  • noxious arthropods preferred examples are aphids; Thripidae; Agromyzidae; Agriotes spp., Leptinotarsa decemlineata, Popillia japonica, Anomala cuprea, Anthonomus grandis, Lissorhoptrus oryzophilus, Frankliniella fusca and Diabrotica spp.; Plutella xylostella; the larvae of
  • Lepidoptera pests Leguminivora glycinivorella and the like.
  • controlling composition of the present invention exert a control effect include the following diseases.
  • Rice diseases Magnaporthe grisea, Cochliobolus miyabeanus, Rhizoctonia solani, and Gibberella fujikuroi.
  • Ustilago nuda Rhynchosporium secalis, Pyrenophora teres, Cochliobolus sativus, Pyrenophora graminea, and Rhizoctonia solani.
  • Citrus plant diseases Diaporthe citri, Elsinoe fawcetti, Penicillium digitatum, P. italicum, Phytophthora parasitica, and Phytophthora citrophthora .
  • Apple diseases Monilinia mali, Valsa ceratosperma, Podosphaera leucotricha, Alternaria alternata apple
  • Peach diseases Monilinia fructicola, Cladosporium carpophilum, and Phomopsis sp.
  • Persimmon diseases Gloeosporium kaki, Cercospora kaki, and ycosphaerella nawae.
  • Sphaerotheca fuliginea Mycosphaerella melonis, Fusarium oxysporum, Pseudoperonospora cubensis, Phytophthora sp., and Pythium sp.
  • Tomato diseases Alternaria solani, Cladosporium fulvum, and Phytophthora infestans.
  • Brassica diseases Alternaria japonica, Cercosporella brassicae, Plasmodiophora brassicae, and Peronospora parasitica .
  • Soybean diseases Cercospora kikuchii, Elsinoe glycines, Diaporthe phaseolorum var. sojae, Septoria glycines, Cercospora sojina, Phakopsora pachyrhizi,
  • Kidney bean diseases Colletotrichum lindemthianum.
  • Peanut diseases Cercospora personata, Cercospora arachidicola, and Sclerotium rolfsii.
  • Pea diseases Erysiphe pisi and Fusarium solani f. sp. pisi .
  • Potato diseases Alternaria solani, Phytophthora infestans, Phytophthora erythroseptica, and Spongospora subterranean f. sp. subterranea.
  • Tobacco diseases Alternaria longipes, Erysiphe cichoracearum, Colletotrichum tabacum, Peronospora tabacina, and Phytophthora nicotianae.
  • Rapeseed diseases Sclerotinia sclerotiorum and
  • Cotton diseases Rhizoctonia solani and Fusarium oxysporum.
  • Bremia lactucae Bremia lactucae, Septoria chrysanthemi-indici, and Puccinia horiana .
  • Pythium spp. (Pythium aphanidermatum, Pythium debarianum, Pythium graminicola, Pythium irregulare, Pythium ultimum) , Botrytis cinerea, and Sclerotinia sclerotiorum. Japanese radish diseases: Alternaria brassicicola .
  • the pest controlling composition of the present invention can be used so as to control pests by application to pests or the place where pests inhabit or the place where pests might inhabit.
  • Examples of the place where pests inhabit or the place where pests might inhabit include foliage of plants, seeds of plants and bulbs of plants. Specifically, scaly bulb, solid bulb, root stock, stem tuber and rhizophore are exemplified as the bulb.
  • the pest controlling method of the present invention is conducted by treatment with the pest controlling
  • composition of the present invention includes a treatment to foliage of plants, such as foliage application; a treatment to seeds, such as seed disinfection or seed coating; and a treatment to bulbs, such as seed tuber.
  • Specific examples of the method for a treatment to foliage of plants in the pest controlling method of the present invention include a treating method of application to surfaces of plants, such as foliage application.
  • the method for a treatment to seeds and the method for a treatment to bulbs in the controlling method of the present invention is, for example, a method of treating seeds and bulbs of plants to be protected from pests with the pest controlling composition of the present invention.
  • Specific examples of the method include a spray treatment in which a suspension of the pest controlling composition of the present invention is sprayed over seed surfaces or bulb surfaces in mist form; a smearing treatment in which a wettable powder, an emulsifiable concentrate or a flowable formulation of the pest controlling composition of the present invention is applied to seeds or bulbs after adding a small amount of water or as it is; an immersion treatment in which seeds are immersed in a solution of the pest controlling composition of the present invention for a given time; a film coating treatment; and a pellet coating treatment.
  • the amount of the composition can vary depending upon the kind of plants to be treated, kind and degree of incidence of pests to be controlled, formulation form, treatment time and
  • clothianidin, tolclophos-methyl, metalaxyl and the present compound (1), and optional compound (s) selected from Group (A) is usually from 1 to 5,000 g, and preferably from 2 to 400 g, per 10,000 m 2 of the place where the plants are cultivated.
  • the treatment is usually conducted by spraying the composition after dilution with water.
  • the total concentration of clothianidin, tolclophos-methyl, metalaxyl and the present compound (1), and optional compound (s) selected from Group (A) is usually from 0.0001 to 3% by weight, and preferably from 0.0005 to 1% by weight.
  • the treatment is usually conducted without dilution.
  • the application is usually conducted in the total amount of clothianidin, tolclophos- methyl, metalaxyl and the present compound (1), and
  • the application is usually conducted in the total amount of clothianidin, tolclophos- methyl, metalaxyl and the present compound (1) , and
  • the pest controlling method of the present invention can be used in crop lands such as upland field, paddy field, and orchard.
  • composition of the present invention can be used in crop lands where "plants" listed below are cultivated so as to control pests in the crop lands:
  • agricultural crops corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, pea, kidney bean, peanut, sarrazin, sugar beet, rapeseed, sunflower, sugar cane, tobacco and the like;
  • Solanaceae vegetables eggplant, tomato, green pepper, hot pepper, potato, etc.
  • Cucurbitaceae vegetables cucumber, pumpkin, zucchini, watermelon, melon, squash, etc.
  • Cruciferae vegetables Japanese radish, turnip, horseradish, kohlrabi, Chinese cabbage, cabbage, brown mustard, broccoli, cauliflower, etc.
  • Compositae vegetables burdock, garland chrysanthemum, artichoke, lettuce, etc.
  • Liliaceae vegetables Welsh onion, onion, garlic, asparagus, etc.
  • Umbelliferae vegetables carrot, parsley, celery, parsnip, etc.
  • Chenopodiaceae vegetables spinach, Swiss chard, etc.
  • Labiatae vegetables Japanese basil, mint, basil, etc.
  • strawberry sweat potato, yam, aroid, etc .
  • Labiatae vegetables Japanese basil, mint, basil, etc.
  • fruit trees pomaceous fruits (apple, common pear, Japanese pear, Chinese quince, quince, etc.), stone fleshy fruits (peach, plum, nectarine, Japanese plum, cherry, apricot, prune, etc.), citrus plants (Satsuma mandarin, orange, lemon, lime, grapefruit, etc.), nuts (chestnut, walnut, hazel nut, almond, pistachio, cashew nut, macadamia nut, etc.), berry fruits (blueberry, cranberry, blackberry, raspberry, etc.), grape, persimmon, olive, loquat, banana, coffee, date, coconut, etc.; and
  • flowering trees and shrubs street trees (ash tree, birch, dogwood, eucalyptus, ginkgo, lilac, maple tree, oak, poplar, cercis, Chinese sweet gum, plane tree, zelkova, Japanese arborvitae, fir tree, Japanese hemlock, needle juniper, pine, spruce, and yew) .
  • corn, wheat, soybean, cotton, rapeseed and sugar beet are exemplified as preferred examples.
  • plants also include those provided with resistance to herbicides, including HPPD inhibitors such as isoxaflutole; ALS inhibitors such as imazethapyr and thifen sulfuronmethyl ; EPSP synthesis enzyme inhibitors such as glyphosate; glutamine synthesis enzyme inhibitors such as glufosinate; acetyl CoA carboxylase inhibitors such as sethoxydim; bromoxynil, dicamba and 2,4-D, by way of a classical breeding method or a genetic recombination technique .
  • HPPD inhibitors such as isoxaflutole
  • ALS inhibitors such as imazethapyr and thifen sulfuronmethyl
  • EPSP synthesis enzyme inhibitors such as glyphosate
  • glutamine synthesis enzyme inhibitors such as glufosinate
  • acetyl CoA carboxylase inhibitors such as sethoxydim
  • bromoxynil, dicamba and 2,4-D by way of a classical breeding method or a genetic
  • plants provided with resistance to an imidazolinone-based ALS inhibitor-type herbicide such as imazethapyr by the classical breeding method include rapeseed, wheat, sunflower, and rice, which have been already on the market under the trade name of Clearfield ® .
  • soybean which has resistance to a sulfonyl urea-based ALS inhibitor-type herbicide such as thifen sulfuronmethyl, and which has been already on the market under the trade name of STS soybean.
  • SR corn as an example of a plant which is provided with resistance to an acetyl CoA carboxylase inhibitor, such as trione oxime-based and aryloxy phenoxypropionic acid-based herbicides, by a classical breeding method.
  • an acetyl CoA carboxylase inhibitor such as trione oxime-based and aryloxy phenoxypropionic acid-based herbicides
  • the plants with resistance to the acetyl CoA inhibitor can be made by introducing such a mutated acetyl CoA carboxylase gene into a plant by means of a genetic recombination technique, or by introducing resistance-providing mutation into acetyl CoA carboxylase of the plant. Further, by introducing base substitution mutation introducing nucleic acid typified by the
  • Examples of the plant provided with resistance by means of a genetic recombination technique include corn, soybean, cotton, rapeseed and sugar beat cultivars
  • rapeseed cultivars provided with resistance to glufosinate by means of a genetic recombination technique, which have been already on the market under the trade name of
  • insecticidal toxins expressed in such transgenic plants include insecticidal proteins derived from Bacillus cereus and Bacillus popilliae; ⁇ -endotoxins derived from Bacillus thuringiensis , e.g. CrylAb, CrylAc, CrylF, CrylFa2, Cry2Ab, Cry3A, Cry3Bbl and Cry9C, and insecticidal proteins such as VIP1, VIP2, VIP3 and VIP3A; insecticidal toxins derived from nematodes; insecticidal toxins produced by animals, such as scorpion toxin, spider toxin, bee toxin and insect-specific neurotoxins ;
  • filamentous fungi toxins filamentous fungi toxins; plant lectins; agglutinin;
  • protease inhibitors such as trypsin inhibitors, serine protease inhibitors, patatin, cystatin and papain
  • ribosome-inactivating proteins such as ricin, corn-RIP, abrin, rufin, sapolin and priodin
  • steroid metabolic enzymes such as 3-hydroxysteroid oxidase
  • channel inhibitors such as sodium channel inhibitors and calcium channel inhibitors; juvenile hormone esterase;
  • diuretic hormone receptors diuretic hormone receptors
  • stilbene synthetase bibenzyl synthetase
  • chitinase and glucanase.
  • ⁇ -endotoxin proteins such as CrylAb, CrylAc, CrylF, CrylFa2, Cry2Ab, Cry3A, Cry3Bbl, Cry9C, Cry34Ab and Cry35Ab
  • hybrid toxins of insecticidal proteins such as VIP1, VIP2 , VIP3 and VIP3A
  • the hybrid toxins can be made by a novel combination of the different domains of such proteins, using a genetic recombination technique.
  • a known partially- deficient toxin is CrylAb, in which a part of an amino acid sequence is deficient.
  • modified toxins one or more amino acids of a natural toxin are replaced.
  • the toxins contained in such transgenic plants impart resistance to insect pests of Coleoptera, insect pests of Hemiptera, insect pests of Diptera, insect pests of
  • transgenic plants containing one or more insecticidal pest-resistant genes and capable of producing one or more toxins are commercially available. Examples of such
  • transgenic plants include YieldGard ® (a corn cultivar expressing a CrylAb toxin) , YieldGard Rootworm ® (a corn cultivar expressing a Cry3Bbl toxin) , YieldGard Plus ® (a corn cultivar expressing CrylAb and Cry3Bbl toxins) ,
  • Herculex ® I (a corn cultivar expressing CrylFa2 toxin and phosphinotrysin N-acetyltransferase (PAT) for imparting resistance to a Glufosinate)
  • NuCOTN33B ® (a cotton cultivar expressing a CrylAc toxin)
  • Bollgard ® I (a cotton cultivar expressing a CrylAc toxin)
  • Bollgard ® II a cotton cultivar expressing CrylAc and Cry2Ab toxins
  • VIPCOT ® (a cotton cultivar expressing a VIP toxin)
  • NewLeaf ® (a potato
  • plants include those provided with a capacity of producing an anti-pathogenic substance having selective activity, using a genetic recombination technique.
  • PR proteins are known (PRPs, described in EP-A-0 392 225) .
  • Examples of the anti-pathogenic substance expressed by these transgenic plants include ion channel inhibitors, such as a sodium channel inhibitor and a calcium channel inhibitor (KP1, KP4 and KP6 toxins produced by viruses are known) ; stilbene synthases; bibenzyl synthases; chitinase; glucanase; and substances produced by microorganisms, such as peptide antibiotics, antibiotics having a heterocyclic ring and protein factors involved in plant disease
  • plants include those provided with useful traits, such as oil component reforming and enhancement of amino acid content, by means of a genetic recombination technique.
  • the crops are exemplified by VISTIVE ® (low linolenic soybean with reduced linolenic acid content) and high-lysine (high-oil) corn (corn with increased lysine or oil content) .
  • the plants further include stacked varieties, which can be made by combining the above classical herbicidal traits or useful traits of herbicide resistant genes, insecticidal pest resistant genes, anti-pathogenic
  • substance-producing genes oil component reforming and enhancement of amino acid content.
  • a flowable formulation is obtained by mixing 5.0 parts of clothianidin, 1.0 parts of tolclophos-methyl , 5.0 parts of metalaxyl, 1.0 part of an R-isomer of the present compound (1), 1.0 part of metconazole, 5.0 parts of
  • ethaboxam 1.5 parts of sorbitan trioleate and 28 parts of an aqueous solution containing 2 parts of polyvinyl alcohol, finely grinding the resultant mixture by a wet grinding method, adding thereto an aqueous solution containing 0.05 parts of xanthan gum and 0.1 parts of aluminum magnesium silicate to make the total volume 90 parts, and then 10 parts of propylene glycol, and stirring and mixing the resulting mixture.
  • a flowable formulation is obtained by mixing 5.0 parts of clothianidin, 1.0 parts of tolclophos-methyl, 5.0 parts of metalaxyl, 1.0 part of a racemic form of the present compound (1), 1.0 part of metconazole, 5.0 parts of ethaboxam, 1.5 parts of sorbitan trioleate and 28 parts of an aqueous solution containing 2 parts of polyvinyl alcohol, finely grinding the resultant mixture by a wet grinding method, adding thereto an aqueous solution containing 0.05 parts of xanthan gum and 0.1 parts of aluminum magnesium silicate to make the total volume 90 parts, and then 10 parts of propylene glycol, and stirring and mixing the resulting mixture.
  • a flowable formulation is obtained by mixing 10.0 parts of clothianidin, 0.2 parts of tolclophos-methyl, 0.2 parts of metalaxyl, 0.4 parts of an R-isomer of the present compound (1), 0.1 parts of metconazole, 0.2 parts of ethaboxam, and 35 parts of a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1:1), and water to make the total volume 100 parts, and finely grinding the resultant mixture by a wet grinding method.
  • a flowable formulation is obtained by mixing 10.0 parts of clothianidin, 0.2 parts of tolclophos-methyl , 0 parts of metalaxyl, 0.4 parts of a racemic form of the present compound (1), 0.1 parts of metconazole, 0.2 parts of ethaboxam, and 35 parts of a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1:1), and water to make the total volume 100 parts, and finely grinding the resultant mixture by a wet grinding method.
  • 100 parts of a wettable powder is obtained by grinding and mixing 20.0 parts of clothianidin, 4.0 part of tolclophos-methyl, 0.4 parts of metalaxyl, 0.8 parts an R-isomer of the present compound (1), 0.8 parts of metconazole, 0.8 parts of ethaboxam, 3 parts of calcium ligninsulfonate, 2 parts of sodium lauryl sulfate and synthetic hydrous silicon oxide (rest) .
  • Wettable powders are obtained by conducting the same operation as in Formulation Example 85, except that
  • 100 parts of a wettable powder is obtained by grinding and mixing 20.0 parts of clothianidin, 4.0 part of tolclophos-methyl, 0.4 parts of metalaxyl, 0.8 parts a racemic form of the present compound (1), 0.8 parts of metconazole, 0.8 parts of ethaboxam, 3 parts of calcium ligninsulfonate, 2 parts of sodium lauryl sulfate and synthetic hydrous silicon oxide (rest) .
  • Wettable powders are obtained by conducting the same operation as in Formulation Example 106, except that compounds described in [Table 6] were used in each amount described in [Table 6] in place of 0.8 parts of metconazole
  • Treated seeds are obtained by smearing 100 kg of Sorghum dry seeds with 500 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as in Formulation Example 1, except that respective flowable formulations produced in Formulation Examples 2 to 84 are used in place of the flowable
  • Treated seeds are obtained by smearing 100 kg of Sorghum dry seeds with 1000 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as in Formulation Example 1, except that respective flowable formulations produced in Formulation Examples 2 to 84 are used in place of the flowable
  • Treated seeds are obtained by smearing 10 kg of corn dry seeds with 40 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as in Formulation Example 1, except that respective flowable formulations produced in Formulation Examples 2 to 84 are used in place of the flowable
  • Treated seeds are obtained by smearing 10 kg of corn dry seeds with 100 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as in Formulation Example 1, except that respective flowable formulations produced in Formulation Examples 2 to 84 are used in place of the flowable
  • Treated . seeds are obtained by dressing 10 kg of corn dry seeds with 50 g of the wettable powder produced in Formulation Example 85.
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Examples 86 to 126 are used in place of the wettable powders produced in Formulation Example 85.
  • Treated seeds are obtained by smearing 10 kg of soybean dry seeds with 50 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing 10 kg of soybean dry seeds with 100 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing 10 kg of cotton dry seeds with 50 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing 10 kg of rapeseed dry seeds with 50 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing 10 kg of rapeseed dry seeds with 100 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing 10 kg of seed potato with 25 ml of the flowable formulation produced in Formulation Example 1 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Treated seeds are obtained by smearing corn seeds with the flowable formulation described in Formulation Example 22 using a rotary seed treating machine (seed dresser, manufactured by Hans-Ulrich Hege GmbH) .
  • the treated seeds are allowed to stand overnight and placed on the soil filled in plastic pots and then covered with the soil mixed with Rhizoctonia solani cultured separately in a bran culture medium. While sprinkling, culture is
  • the non-chemical-treated section Ten days after seeding, the number of seeds that did not show epicotyl emergence is examined and severity is calculated by "Equation 1" shown below.
  • Equation 2 By calculating the control value of the chemical-treated section by "Equation 2" shown below based on the severity of the chemical-treated section and that of the non-chemical-treated section, it can be confirmed that the chemical-treated section exhibits a satisfactory pest control effect.
  • Severity (%) [ (Number of seeds that did not show epicotyl emergence) / (Total number of inoculated seeds)] ⁇ 100 Equation 1
  • Control value (%) [ (A - B) / (A) ] ⁇ 100
  • corn seeds are smeared with the flowable formulation described in Formulation Example 64 in the amount of 5 ⁇ per one corn seed and placed in a 1/10,000 are Wagner pot in which the soil is spread. After growing the plants in a greenhouse for 12 days, five Rhopalosiphum padi are released (hereinafter referred to as the test section) .
  • the test section five Rhopalosiphum padi are released.
  • the control section Using corn seeds which are not treated with the flowable formulation described in Formulation Example 64, seeding, growing and release are conducted in the same manner as in the case of the test section (hereinafter referred to as the control section) .
  • the number of Rhopalosiphum padi is examined with respect to the test section and the control section. As a result, since the number of insects in the test section is smaller than the number of insects in the control section, it is possible to confirm that the test section exerts a satisfactory pest control effect.

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  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Un objet de la présente invention concerne une composition de lutte contre des nuisibles présentant un excellent effet de lutte contre des nuisibles. Une composition de lutte contre des nuisibles contenant de la clothianidine, du tolclophos-méthyle, du métalaxyl et un composé représenté par la formule (1) présente un excellent effet de lutte contre des nuisibles
PCT/JP2010/056282 2010-03-04 2010-03-31 Composition et procédé de lutte contre des nuisibles WO2011108123A2 (fr)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20150264925A1 (en) * 2010-10-14 2015-09-24 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US20150313218A1 (en) * 2012-12-21 2015-11-05 Sumitomo Chemical Company, Limited Method for increasing yield of crop seeds or fruits in number or weight
US9179671B2 (en) 2010-10-14 2015-11-10 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
CN107094766A (zh) * 2017-05-11 2017-08-29 深圳诺普信农化股份有限公司 一种种子处理剂
US10631540B2 (en) 2015-12-01 2020-04-28 Sumitomo Chemical Company, Limited Plant disease control composition, and plant disease control method

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010275325A (ja) * 2010-09-14 2010-12-09 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物の防除方法
JP2010280731A (ja) * 2010-09-22 2010-12-16 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物の防除方法
JP2012102076A (ja) * 2010-10-14 2012-05-31 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物防除方法
JP2012102075A (ja) * 2010-10-14 2012-05-31 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物防除方法
JP2012136503A (ja) * 2010-10-14 2012-07-19 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物防除方法
JP2012106984A (ja) * 2010-10-28 2012-06-07 Sumitomo Chemical Co Ltd 有害生物防除用組成物及び有害生物防除方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0754672B1 (fr) * 1994-04-06 2000-10-11 Shionogi & Co., Ltd. Derive d'acide phenylacetique a substitution gamma, son procede d'obtention et bactericide agricole le contenant
DE102005015850A1 (de) * 2005-04-07 2006-10-12 Bayer Cropscience Ag Synergistische fungizide Wirkstoffkombinationen

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
GURA T.: "Repairing the Genome's Spelling Mistakes", SCIENCE, vol. 285, 1999, pages 316 - 318
PROCEEDING OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, vol. 87, 1990, pages 7175 - 7179
WEED SCIENCE, vol. 53, 2005, pages 728 - 746

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US20150264925A1 (en) * 2010-10-14 2015-09-24 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US9179671B2 (en) 2010-10-14 2015-11-10 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US9668478B2 (en) 2010-10-14 2017-06-06 Sumitomo Chemical Company, Limited Pest controlling composition and method for controlling pest
US20150313218A1 (en) * 2012-12-21 2015-11-05 Sumitomo Chemical Company, Limited Method for increasing yield of crop seeds or fruits in number or weight
EP2936981A4 (fr) * 2012-12-21 2016-09-21 Sumitomo Chemical Co Procédé pour augmenter le nombre ou le poids de graines ou de fruits
US10485233B2 (en) 2012-12-21 2019-11-26 Sumitomo Chemical Company, Limited Method for increasing yield of crop seeds or fruits in number or weight
US10631540B2 (en) 2015-12-01 2020-04-28 Sumitomo Chemical Company, Limited Plant disease control composition, and plant disease control method
CN107094766A (zh) * 2017-05-11 2017-08-29 深圳诺普信农化股份有限公司 一种种子处理剂

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