+

WO2011108125A2 - Composition et procédé de lutte contre des nuisibles - Google Patents

Composition et procédé de lutte contre des nuisibles Download PDF

Info

Publication number
WO2011108125A2
WO2011108125A2 PCT/JP2010/056284 JP2010056284W WO2011108125A2 WO 2011108125 A2 WO2011108125 A2 WO 2011108125A2 JP 2010056284 W JP2010056284 W JP 2010056284W WO 2011108125 A2 WO2011108125 A2 WO 2011108125A2
Authority
WO
WIPO (PCT)
Prior art keywords
pests
seeds
parts
formulation
pest
Prior art date
Application number
PCT/JP2010/056284
Other languages
English (en)
Other versions
WO2011108125A3 (fr
Inventor
Soichi Tanaka
Mayuko Ozawa
So Kiguchi
Atsushi Iwata
Original Assignee
Sumitomo Chemical Company, Limited
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sumitomo Chemical Company, Limited filed Critical Sumitomo Chemical Company, Limited
Publication of WO2011108125A2 publication Critical patent/WO2011108125A2/fr
Publication of WO2011108125A3 publication Critical patent/WO2011108125A3/fr

Links

Classifications

    • 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/64Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647Triazoles; Hydrogenated triazoles
    • A01N43/6531,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
    • 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
    • A01N57/16Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-oxygen bonds or phosphorus-to-sulfur bonds containing heterocyclic 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, metconazole, metalaxyl and tolclophos-methyl has an excellent control effect against pests, thus leading to the present invention.
  • the present invention provides [1] to [9] shown below:
  • a pest controlling composition containing clothianidin, metconazole, metalaxyl and tolclophos-methyl
  • Group (A) consisting of:
  • pyraclostrobin orysastrobin, 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, metconazole, metalaxyl and tolclophos-methyl .
  • the total content of metconazole, metalaxyl and tolclophos-methyl is usually from 2 to
  • each content of metconazole, metalaxyl and tolclophos-methyl is usually from 5 to 20,000 parts by weight based on 1,000 parts by weight of metconazole.
  • the pest controlling composition of the present invention can contain, in addition to clothianidin,
  • Group (A) consisting of:
  • pyraclostrobin orysastrobin, carboxin, oxycarboxin,
  • azoxystrobin fluoxastrobin, trifloxystrobin, pyraclostrobin, orysastrobin, carboxin, oxycarboxin,
  • thiabendazole are known compounds and are described, for example, in "THE PESTICIDE MANUAL - 15th EDITION (published by BCPC) ISBN 1901396188", page 62, page 538, page 1167, page 971, page 840, page 164, page 855, page 520, page 1132, page 154, page 1128 and page 1109. These compounds are obtained from commercially available formulations, or obtained by production using a known method.
  • 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, metconazole, metalaxyl and tolclophos-methyl, and optional compound(s) selected from Group (A), but is usually
  • composition can be used as a pest control agent as it is, or after adding other inert ingredients.
  • the total content of clothianidin, metconazole, metalaxyl and tolclophos-methyl, 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 cottonseed oil; petroleum-based aliphatic hydrocarbons;
  • 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 arabic; 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 BHT.
  • water-soluble polymers such as polyvinyl alcohol and polyvinyl pyrrolidone
  • gum arabic such as 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 BHT.
  • the pest controlling composition of the present invention can be used so as to protect plants from
  • pests for example, noxious arthropods such as noxious insects and noxious mites, and plant
  • Examples of noxious arthropods on which the pest controlling composition of the present invention exert a control effect include: 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, yzus 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 Phthoriitiaea 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.
  • 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
  • Gymnosporangium haraeanum and Phytophtora cactorum.
  • Peach diseases Monilinia fructicola, Cladosporium carpophilum, and Phomopsis sp.
  • Persimmon diseases Gloeosporium kaki, Cercospora kaki, and Mycosphaerella 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.
  • Banana diseases Mycosphaerella fijiensis and ycosphaerella musicola.
  • Seed diseases and diseases at early growth stage of various plants caused by fungi which belong to the genus Aspergillus, the genus Penicillium, the genus Fusarium, the genus Gibberella, the genus Tricoderma, the genus
  • Thielaviopsis the genus Rhizopus, the genus Mucor, the genus Corticium, the genus Phoma, the genus Rhizoctonia, the genus Diplodia and the like.
  • 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, metconazole, metalaxyl and tolclophos-methyl, 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, metconazole, metalaxyl and tolclophos- methyl, 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, metconazole, metalaxyl and tolclophos-methyl, and optional compound (s) selected from Group (A) within a range from 0.001 to 20 g, and preferably from 0.01 to 5 g, based on 1 kg of seeds.
  • the application is usually conducted in the total amount of clothianidin, metconazole, metalaxyl and tolclophos-methyl, and optional compound (s) selected from Group (A) within a range from 0.001 to 20 g, and preferably from 0.01 to 5 g, based on 1 kg of bulbs.
  • 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 Wang 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) .
  • rapeseed and sugar beet are exemplified as preferred
  • 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 sethoxydina; 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 sethoxydina
  • bromoxynil, dicamba and 2, 4-D by way of a classical breeding method or a genetic recomb
  • Examples of the "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 thifensulfuron—methyl by the classical breeding method, 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
  • Examples of the plant provided with resistance to the acetyl CoA carboxylase inhibitor are described in the proceeding of the National Academy of Sciences of the United States of America (Proc. Natl. Acad. Sci. USA) , Vol. 87, pp. 7175-7179 (1990) and the like.
  • mutated acetyl CoA carboxylase which is resistant to the acetyl CoA carboxylase inhibitor, is reported in the Weed Science, Vol. 53, pp.
  • the plants with resistance to the acetyl CoA carboxylase 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
  • nucleic acid typified by a chimeraplasty
  • Examples of the plant provided with resistance by means of a genetic recombination technique include corn, soybean, cotton, rapeseed and sugar beet 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
  • plants also include those which have been made capable of synthesizing selective toxins known as genus Bacillus, using a genetic recombination technique.
  • 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 VIPI, 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, partially deficient toxins, and modified toxins .
  • the hybrid toxins can be made by a novel
  • 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 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
  • Agrisure ® CB Advantage (Btll corn borer (CB) property)
  • Protecta ® .
  • 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) . These anti-pathogenic substances and transgenic plants producing the same are described in EP-A-0 392 225, WO 95/33818, and EP-A-0 353 191.
  • 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 (KPl, KP4 and KP6 toxins produced by viruses are known) ; stilbene synthases; bibenzyl synthases; chitinase; glucanase; PR proteins; and substances produced by ion channel inhibitors, such as a sodium channel inhibitor and a calcium channel inhibitor (KPl, KP4 and KP6 toxins produced by viruses are known) ; stilbene synthases; bibenzyl synthases; chitinase; glucanase; PR proteins; and substances produced by ion channel inhibitors, such as a sodium channel inhibitor and a calcium channel inhibitor (KPl, KP4 and KP6 toxins produced by viruses are known) ; stilbene synthases; bibenzyl synthases; chitinase; glucanase; PR proteins; and substances produced by ion channel inhibitor
  • microorganisms such as peptide antibiotics, antibiotics having a heterocyclic ring and protein factors involved in plant disease resistance (called as plant disease resistant genes and described in WO 03/000906) .
  • plant disease resistant genes called as plant disease resistant genes and described in WO 03/000906 .
  • plant disease resistant genes called as plant disease resistant genes and described in WO 03/000906 .
  • anti- pathogenic substances and transgenic plants producing the same are described in EP-A-0 392 225, WO 95/33818, and EP- A-0 353 191.
  • 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
  • a flowable formulation is obtained by mixing 5.0 parts of clothianidin, 1.0 part of metconazole, 5.0 parts of metalaxyl, 1.0 part of tolclophos-methyl, 0.5 parts of azoxystrobin, 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, 0.1 parts of metconazole, 0.2 parts of metalaxyl, 0.2 parts of tolclophos-methyl , 0.2 parts of azoxystrobin, 0.2 parts of ethaboxam, 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 wettable powder (100 parts) is obtained by grinding and mixing 20.0 parts of clothianidin, 0.8 parts of
  • metconazole 0.4 parts of metalaxyl, 4.0 parts of
  • tolclophos-methyl 0.4 parts of azoxystrobin, 0.8 parts of ethaboxam, 3 parts of calcium lignin sulfonate, 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 25, except that
  • 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 described above, except that
  • 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 described above, except that respective flowable formulations produced in Formulation Examples 2 to 24 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 described above, except that
  • 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 described above, except that
  • Treated seeds are obtained by dressing 10 kg of corn dry seeds with 50 g of the wettable powder produced in Formulation Example 25.
  • Respective treated seeds are obtained by conducting the same operation as described above, except that
  • Examples 26 to 36 are used in place of the wettable powder produced in Formulation Example 25.
  • 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 13 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 wettable powder described in Formulation Example 26 in the amount of 5 ⁇ per one corn seed and placed in 1/10,000 are Wagner pot in which the soil is spread. After growing the plant in a greenhouse for 12 days, five
  • Rhopalosiphum padi are released (hereinafter referred to as the test section) .
  • the test section Using corn seeds which are not treated with the wettable powder described in Formulation Example 26, 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.

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Dentistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Agronomy & Crop Science (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
  • Catching Or Destruction (AREA)
  • Pretreatment Of Seeds And Plants (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 metconazole, du métalaxyle, du tolclophos-méthyle présente un excellent effet de lutte contre des nuisibles.
PCT/JP2010/056284 2010-03-04 2010-03-31 Composition et procédé de lutte contre des nuisibles WO2011108125A2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2010-047745 2010-03-04
JP2010047745A JP2010159277A (ja) 2010-03-04 2010-03-04 有害生物防除組成物及び有害生物の防除方法

Publications (2)

Publication Number Publication Date
WO2011108125A2 true WO2011108125A2 (fr) 2011-09-09
WO2011108125A3 WO2011108125A3 (fr) 2012-05-31

Family

ID=42576713

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2010/056284 WO2011108125A2 (fr) 2010-03-04 2010-03-31 Composition et procédé de lutte contre des nuisibles

Country Status (2)

Country Link
JP (1) JP2010159277A (fr)
WO (1) WO2011108125A2 (fr)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104186511A (zh) * 2014-08-20 2014-12-10 石家庄市深泰化工有限公司 一种含有吡唑醚菌酯和噻唑菌胺的杀菌组合物
US10631540B2 (en) 2015-12-01 2020-04-28 Sumitomo Chemical Company, Limited Plant disease control composition, and plant disease control method
US11045564B2 (en) 2013-10-18 2021-06-29 Deutsches Krebsforschungszentrum Labeled inhibitors of prostate specific membrane antigen (PSMA) as agents for the treatment of prostate cancer
US11155800B2 (en) 2010-02-25 2021-10-26 Purdue Research Foundation PSMA binding ligand-linker conjugates and methods for using
US12178892B2 (en) 2013-11-14 2024-12-31 Purdue Research Foundation Compounds for positron emission tomography
US12208102B2 (en) 2018-04-17 2025-01-28 Endocyte, Inc. Methods of treating cancer

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5629881B2 (ja) * 2010-08-11 2014-11-26 住友化学株式会社 有害節足動物防除組成物及び有害節足動物の防除方法
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
WO2012077077A1 (fr) * 2010-12-08 2012-06-14 Basf Se Mélanges fongicides
CN105638718B (zh) * 2012-03-08 2018-06-26 陕西韦尔奇作物保护有限公司 一种含萎锈灵的农药组合物
CN105766961B (zh) * 2012-09-28 2018-10-09 沈阳中化农药化工研发有限公司 一种含吡唑类化合物与咪唑类化合物的杀真菌组合物
CN104938510B (zh) * 2015-07-08 2017-10-10 安徽省农业科学院植物保护与农产品质量安全研究所 一种含吡唑醚菌酯和噻菌灵的杀菌组合物

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
PROC. NATL. ACAD. SCI. USA, vol. 87, 1990, pages 7175 - 7179
WEED SCIENCE, vol. 53, 2005, pages 728 - 746

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US11155800B2 (en) 2010-02-25 2021-10-26 Purdue Research Foundation PSMA binding ligand-linker conjugates and methods for using
US12091693B2 (en) 2010-02-25 2024-09-17 Purdue Research Foundation PSMA binding ligand-linker conjugates and methods for using
US11045564B2 (en) 2013-10-18 2021-06-29 Deutsches Krebsforschungszentrum Labeled inhibitors of prostate specific membrane antigen (PSMA) as agents for the treatment of prostate cancer
US11931430B2 (en) 2013-10-18 2024-03-19 Novartis Ag Labeled inhibitors of prostate specific membrane antigen (PSMA) as agents for the treatment of prostate cancer
US12178892B2 (en) 2013-11-14 2024-12-31 Purdue Research Foundation Compounds for positron emission tomography
CN104186511A (zh) * 2014-08-20 2014-12-10 石家庄市深泰化工有限公司 一种含有吡唑醚菌酯和噻唑菌胺的杀菌组合物
US10631540B2 (en) 2015-12-01 2020-04-28 Sumitomo Chemical Company, Limited Plant disease control composition, and plant disease control method
US12208102B2 (en) 2018-04-17 2025-01-28 Endocyte, Inc. Methods of treating cancer

Also Published As

Publication number Publication date
WO2011108125A3 (fr) 2012-05-31
JP2010159277A (ja) 2010-07-22

Similar Documents

Publication Publication Date Title
WO2012117572A1 (fr) Composition pesticide et procédé de lutte contre les parasites
WO2011108125A2 (fr) Composition et procédé de lutte contre des nuisibles
CA2737884C (fr) Composition pesticide comprenant un derive de l'acide alpha-alcoxyphenyle acetique et un compose neonicotinoide
WO2011108123A2 (fr) Composition et procédé de lutte contre des nuisibles
CA2744006C (fr) Composition pour maitrise des nuisibles et methode de maitrise des nuisibles
WO2011108124A2 (fr) Composition et procédé de lutte contre des nuisibles
EP2647288B1 (fr) Composition et procédé de lutte contre les nuisibles
US8853127B2 (en) Composition and method for controlling pests
WO2012039068A1 (fr) Composition antiparasitaire et procédé antiparasitaire
WO2011108122A2 (fr) Procédé et composition pour lutter contre les parasites
US9012361B2 (en) Composition and method for controlling pests
WO2012035670A1 (fr) Composition de lutte contre des animaux nuisibles et procédé de lutte contre des animaux nuisibles

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 10719128

Country of ref document: EP

Kind code of ref document: A2

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 10719128

Country of ref document: EP

Kind code of ref document: A2

点击 这是indexloc提供的php浏览器服务,不要输入任何密码和下载