WO2014098201A1 - 作物の種子もしくは果実の数又は重量の増収方法 - Google Patents
作物の種子もしくは果実の数又は重量の増収方法 Download PDFInfo
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- WO2014098201A1 WO2014098201A1 PCT/JP2013/084172 JP2013084172W WO2014098201A1 WO 2014098201 A1 WO2014098201 A1 WO 2014098201A1 JP 2013084172 W JP2013084172 W JP 2013084172W WO 2014098201 A1 WO2014098201 A1 WO 2014098201A1
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, 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
- A01N37/36—Biocides, 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
- A01N37/38—Biocides, 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
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, 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
- A01N37/18—Biocides, 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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Definitions
- the present invention relates to a method for increasing the number or weight of crop seeds or fruits.
- Patent Document 1 ⁇ -substituted phenylacetic acid compounds
- Patent Document 2 Non-Patent Document 1 and Patent Document 2
- bactericides there is always a need for methods to increase the number or weight of crop seeds or fruits.
- An object of the present invention is to provide a method for increasing the number or weight of crop seeds or fruits.
- the present inventors have found a method for increasing the number or weight of seeds or fruits by treating a crop of the compound represented by the formula (1) and at least one compound selected from the group (A). It was. That is, the present invention is as follows. [1] A method for increasing the number or weight of crop seeds or fruits, comprising a step of treating an effective amount of a compound represented by formula (1) and at least one compound selected from group (A) into a crop .
- [4] Increase in yield according to [1], wherein the at least one compound selected from the group (A) is azoxystrobin, dimoxystrobin, pyraclostrobin, trifloxystrobin or picoxystrobin Method.
- [6] The method for increasing yield according to any one of [1] to [5], wherein the compound represented by the formula (1) has an absolute configuration of R.
- [7] The method for increasing yield according to any one of [1] to [6], wherein the crop is rapeseed, rice, corn, wheat, barley, kidney bean, soybean, peach, apple, or pear.
- Group (A) Use of the compound represented by the formula (1) and at least one compound selected from the group (A) as a yield-increasing agent for the number or weight of crop seeds or fruits.
- the method for increasing yield according to the present invention includes a compound represented by formula (1) (hereinafter sometimes referred to as “compound (1)”) and a group ( A method for treating a crop with an effective amount of at least one compound selected from A) (hereinafter sometimes referred to as “compound (A)”).
- Group (A) from tebuconazole, prothioconazole, cyproconazole, metconazole, boscalid, fluopyram, floxapyroxad, azoxystrobin, dimoxystrobin, pyraclostrobin, trifloxystrobin and picoxystrobin A group.
- Compound (1) is a known compound and can be produced, for example, by the method described in International Publication No. 95/27693 pamphlet, International Publication No. 02/10101, or the like.
- Tebuconazole, prothioconazole, cyproconazole, metconazole, boscalid, fluopyram, azoxystrobin, dimoxystrobin, pyraclostrobin, trifloxystrobin and picoxystrobin are all known compounds, for example, ⁇ The Pesticide Manual 15th edition (The Pesticide Manual Fifteenth edition) published by British Crop Protection Council (BCPC), pages 1072, 965, 287, 749, 121, 535, 62, 383 Page 971, page 1167, and page 910. Floxapyroxad is described in WO 2007/018416. These compounds can be obtained from commercially available preparations or produced by known methods.
- Compound (1) has one asymmetric carbon, and any compound having an enantiomeric ratio in this method can be used as compound (1). From the viewpoint of activity, the compound (1) having an absolute configuration of R is preferably used.
- the compound (1) and the compound (A) may be used alone, but it is preferable to use a compound obtained by simply mixing the compound (1) and the compound (A). , Compound (A), and an inert carrier, and if necessary, add a surfactant or other formulation adjuvant, oil, emulsion, flowable, wettable powder, wettable powder, powder It is more preferable to use those formulated into granules or the like.
- the total amount of the compound (1) and the compound (A) is usually 0.1 to 99% by weight, preferably 0.2 to 90% by weight, more preferably 1 to 80% by weight.
- solid carriers used in the formulation include kaolin clay, attapulgite clay, bentonite, montmorillonite, acid clay, pyrophyllite, talc, diatoms, calcite and other minerals, corn cob flour, walnut shells
- solid carriers include natural organic substances such as powder, synthetic organic substances such as urea, salts such as calcium carbonate and ammonium sulfate, and fine powders or granular materials made of synthetic inorganic substances such as synthetic silicon hydroxide.
- liquid carrier examples include xylene, Aromatic hydrocarbons such as 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 coal Hydrogen, esters, dimethyl sulfoxide, acetonitrile and water.
- Aromatic hydrocarbons such as 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 coal Hydrogen esters, dimethyl sulfoxide, acetonitrile and water.
- Surfactants include, for example, negative alkyl sulfate salts, alkyl aryl sulfonates, dialkyl sulfosuccinates, polyoxyethylene alkyl aryl ether phosphate esters, lignin sulfonates, naphthalene sulfonate formaldehyde polycondensates, and the like.
- Examples include ionic surfactants, and nonionic surfactants such as polyoxyethylene alkyl aryl ethers, polyoxyethylene alkyl polyoxypropylene block copolymers, and sorbitan fatty acid esters, and cationic surfactants such as alkyltrimethylammonium salts. .
- formulation adjuvants include, for example, 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, aluminum magnesium silicate, Examples thereof include inorganic substances such as alumina sol, preservatives, colorants and stabilizers such as PAP (isopropyl acid phosphate) and BHT.
- 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
- aluminum magnesium silicate examples thereof include inorganic substances such as alumina sol, preservatives, colorants and stabilizers such as PAP (isopropyl acid phosphate) and BHT.
- PAP isopropyl acid phosphate
- the compound (1) and the compound (A) are separately formulated by the above-described method, etc., and further diluted with water as necessary, and each formulation or diluent is mixed. It can also be used.
- this method can be applied by mixing with one or more other fungicides or insecticides.
- fungicides or insecticides Known germicides and insecticides can be used.
- Specific treatment methods for the crops in this method include treatment of foliage such as foliage spraying, treatment of crops such as soil treatment, cultivation of crops, treatment of crop seeds such as seed disinfection, etc. Is mentioned.
- Examples of the treatment for the foliage of the crop in the present method include a treatment method applied to the surface of the crop such as foliage spray and trunk spray.
- Examples of the treatment method for directly absorbing the crop before transplantation include a method of immersing the whole crop or the root.
- what was formulated with a solid carrier such as mineral powder may be attached to the root.
- Examples of the treatment of the crops in the present method include the application to the soil, the mixing of the soil, and the chemical irrigation to the soil (chemical irrigation, soil injection, chemical drip). Planting holes, rowing, near planting holes, near rowing, whole area of plantation, plant land border, between stocks, under trunk, trunk trunk, cultivation soil, nursery box, nursery tray, nursery, etc.
- sowing time before sowing, sowing, immediately after sowing, seedling season, before planting, at the time of planting, and after planting (early flowering period, flowering period, flowering end period, reproductive growth period).
- an active ingredient may be processed to a crop and soil simultaneously, and solid fertilizers, such as a paste fertilizer containing an active ingredient, may be applied to soil.
- you may mix with an irrigation liquid for example, the injection
- the irrigation liquid and the active ingredient can be mixed in advance, and can be treated using an appropriate irrigation method such as the above irrigation method or other watering or watering.
- the treatment of crop seeds in this method is, for example, a method of treating the present composition on crop seeds, bulbs, etc., for example, a suspension of compound (1) and compound (A) is atomized. A small amount of water is added to the wettable powder, emulsion or flowable of compound (1) and compound (A), or applied to the seed or bulb as it is. Examples thereof include smearing treatment, dipping treatment in which seeds are immersed in a solution of compound (1) and compound (A) for a certain period of time, film coating treatment, and pellet coating treatment.
- the amount of compound (1) and compound (A) applied depends on the type of crop to be treated, the type and degree of occurrence of plant diseases to be controlled, formulation, application time, application method, application location, weather conditions, etc. Although different, in the case of processing to the foliage of the crop or when processing to the cultivation place, the total amount of the compound (1) and the compound (A) (hereinafter referred to as “the amount of the active ingredient”) is 1000 m.
- the amount per 2 is usually 1 to 500 g, preferably 2 to 200 g, more preferably 10 to 100 g.
- the amount of the active ingredient is usually 0.001 to 10 g, preferably 0.01 to 1 g, per 1 kg of seeds.
- Emulsions, wettable powders, suspensions, etc. are usually diluted with water and sprayed. In this case, the concentration of the active ingredient is usually 0.0005 to 2% by weight, preferably 0.005 to 1% by weight. Powders, granules, etc. are usually processed without dilution.
- Agricultural crops corn, rice, wheat, barley, rye, oat, sorghum, cotton, soybean, adzuki beans, kidney beans, peanuts, buckwheat, sugar beet, rapeseed, sunflower, sugarcane, tobacco, etc.
- Vegetables Eggplant vegetables (eggplant, tomatoes, peppers, peppers, potatoes, etc.), cucurbits vegetables (cucumbers, pumpkins, zucchini, watermelon, melon, squash, etc.), cruciferous vegetables (radish, turnip, horseradish, kohlrabi, Chinese cabbage) , Cabbage, mustard, broccoli, cauliflower, etc.), asteraceae vegetables (burdock, garlic, artichoke, lettuce, etc.), liliaceae vegetables (leek, onion, garlic, asparagus), celery family vegetables (carrot, parsley, celery, USA Bowfish, etc.), red crustacean vegetables (spinach, chard, etc.), perilla vegetables (perilla, mint, basil, etc.), strawberries, sweet potatoes, yam, taros, etc.
- Fruit trees berries (apples, pears, Japanese pears, quince, quince, etc.), nuclear fruits (peaches, plums, nectarines, ume, sweet cherry, apricot, prunes, etc.) ), Nuts (chestnut, walnut, hazel, almond, pistachio, cashew nut, macadamia nut, etc.), berries (blueberry, cranberry, blackberry, raspberry, etc.), grape, oyster, olive, loquat, banana, coffee, Date palm, coconut palm, etc. Trees other than fruit trees; cha, mulberry, etc.
- crop includes genetically modified plants.
- crop rapeseed, rice, corn, wheat, barley, kidney bean, soybean, peach, apple, or pear are preferable examples. According to the present invention, it is possible to increase the number or weight of crop seeds or fruits.
- Formulation Example 1 5 parts of compound (1), 5 parts of compound (A), 35 parts of a mixture of white carbon and polyoxyethylene alkyl ether sulfate ammonium salt (weight ratio 1: 1) and 55 parts of water are mixed, and wet pulverization is performed. Each flowable preparation is obtained by pulverization.
- Formulation Example 2 After mixing 10 parts of compound (1), 5 parts of compound (A), 1.5 parts of sorbitan trioleate, and 2 parts of an aqueous solution containing 2 parts of polyvinyl alcohol, and finely pulverizing by a wet pulverization method, To this, 45.50 parts of an aqueous solution containing 0.05 part of xanthan gum and 0.1 part of aluminum magnesium silicate is added, and 10 parts of propylene glycol is further added and stirred to obtain a flowable preparation.
- Each wettable powder is obtained by thoroughly pulverizing and mixing 10 parts of Compound (1), 40 parts of Compound (A), 3 parts of calcium lignin sulfonate, 2 parts of sodium lauryl sulfate and 45 parts of synthetic silicon hydroxide.
- Test example 1 On September 3, 2010, rapeseed seeds were sown and grown at a density of 3.5 kg / ha. A 25% flowable formulation of compound (1) and tebuconazole (: Horizon (registered trademark) 25% EW) were diluted with water, and the mixed composition was adjusted so that compound (1) and tebuconazole were each 150 g / ha. On May 19, 2011, the rapeseed was treated with foliage at the flowering stage (growth stage BBCH65 (Bisammlung Supreme Bundssortenamt and Chemical industry (BBCH scale))). The throughput was 200 L / ha. The test area was 3 ⁇ 8 m, and the test group treated with the drug by the above operation was defined as the process group.
- medical agent treatment of the same test area was made into the no-treatment group.
- rapeseed seeds were harvested and the yield per hectare was investigated.
- the water content of the rapeseed seed to be investigated was 9%.
- a yield of 4.3 tons / ha was obtained in the treated area, whereas it was 3.8 tons / ha in the untreated area.
- the yield of crop seeds can be increased.
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Abstract
Description
即ち、本発明は次の通りである。
〔1〕 式(1)で示される化合物と、群(A)から選ばれる少なくとも1種の化合物との有効量を、作物に処理する工程を含む作物の種子又は果実の数又は重量の増収方法。
群(A):テブコナゾール、プロチオコナゾール、シプロコナゾール、メトコナゾール、ボスカリド、フルオピラム、フルキサピロキサド、アゾキシストロビン、ジモキシストロビン、ピラクロストロビン、トリフロキシストロビン及びピコキシストロビンからなる群。
〔2〕 群(A)から選ばれる少なくとも1種の化合物が、テブコナゾール、プロチオコナゾール、シプロコナゾールまたはメトコナゾールである、[1]に記載の増収方法。
〔3〕 群(A)から選ばれる少なくとも1種の化合物が、ボスカリド、フルオピラム、またはフルキサピロキサドである、[1]に記載の増収方法。
〔4〕 群(A)から選ばれる少なくとも1種の化合物が、アゾキシストロビン、ジモキシストロビン、ピラクロストロビン、トリフロキシストロビンまたはピコキシストロビンである、[1]に記載の増収方法。
〔5〕 式(1)で示される化合物と、群(A)から選ばれる少なくとも1種の化合物との重量比が、式(1)で示される化合物/群(A)から選ばれる化合物=0.0125/1~500/1である[1]~[4]いずれかに記載の増収方法。
〔6〕 式(1)で示される化合物が、Rの絶対立体配置を有する、[1]~[5]いずれかに記載の増収方法。
〔7〕 作物が、ナタネ、イネ、トウモロコシ、コムギ、オオムギ、インゲンマメ、ダイズ、モモ、リンゴ、またはセイヨウナシである[1]~[6]いずれかに記載の増収方法。
群(A):テブコナゾール、プロチオコナゾール、シプロコナゾール、メトコナゾール、ボスカリド、フルオピラム、フルキサピロキサド、アゾキシストロビン、ジモキシストロビン、ピラクロストロビン、トリフロキシストロビン及びピコキシストロビンからなる群。
本方法において、化合物(1)と化合物(A)との合計量は通常0.1~99重量%、好ましくは0.2~90重量%、より好ましくは1~80重量%である。
本方法における作物の栽培地への処理としては、例えば、土壌への散布、土壌混和、土壌への薬液潅注(薬液潅水、土壌注入、薬液ドリップ)が挙げられ、処理する場所としては、例えば、植穴、作条、植穴付近、作条付近、栽培地の全面、植物地際部、株間、樹幹下、主幹畦、培土、育苗箱、育苗トレイ、苗床等が挙げられ、処理時期としては播種前、播種時、播種直後、育苗期、定植前、定植時、及び定植後の生育期等(開花初期、開花盛期、開花終期、生殖成長期)が挙げられる。また、上記栽培地への処理において、有効成分を作物と土壌に同時に処理してもよく、有効成分を含有するペースト肥料等の固形肥料を土壌へ施用してもよい。また、潅水液に混合してもよく、例えば、潅水設備(潅水チューブ、潅水パイプ、スプリンクラー等)への注入、条間湛水液への混入、水耕液への混入等が挙げられる。また、あらかじめ潅水液と有効成分を混合し、例えば、上記潅水方法やそれ以外の散水、湛水等のしかるべき潅水方法を用いて処理することができる。
本方法における作物の種子への処理としては、例えば、作物の種子、球根等に本組成物を処理する方法であって、例えば、化合物(1)と化合物(A)の懸濁液を霧状にして種子表面もしくは球根表面に吹きつける吹きつけ処理、化合物(1)と化合物(A)の水和剤、乳剤又はフロアブル剤等に少量の水を加えるか又はそのままで種子もしくは球根に塗付する塗沫処理、化合物(1)と化合物(A)の溶液に一定時間種子を浸漬する浸漬処理、フィルムコート処理、ペレットコート処理が挙げられる。
乳剤、水和剤、懸濁剤等は通常水で希釈して散布する。この場合、本有効成分量の濃度は通常0.0005~2重量%、好ましくは0.005~1重量%である。粉剤、粒剤等は通常希釈することなくそのまま処理する。
野菜;ナス科野菜(ナス、トマト、ピーマン、トウガラシ、ジャガイモ等)、ウリ科野菜(キュウリ、カボチャ、ズッキーニ、スイカ、メロン、スカッシュ等)、アブラナ科野菜(ダイコン、カブ、セイヨウワサビ、コールラビ、ハクサイ、キャベツ、カラシナ、ブロッコリー、カリフラワー等)、キク科野菜(ゴボウ、シュンギク、アーティチョーク、レタス等)、ユリ科野菜(ネギ、タマネギ、ニンニク、アスパラガス)、セリ科野菜(ニンジン、パセリ、セロリ、アメリカボウフウ等)、アカザ科野菜(ホウレンソウ、フダンソウ等)、シソ科野菜(シソ、ミント、バジル等)、イチゴ、サツマイモ、ヤマノイモ、サトイモ等、
果樹:仁果類(リンゴ、セイヨウナシ、ニホンナシ、カリン、マルメロ等)、核果類(モモ、スモモ、ネクタリン、ウメ、オウトウ、アンズ、プルーン等)、カンキツ類(ウンシュウミカン、オレンジ、レモン、ライム、グレープフルーツ等)、堅果類(クリ、クルミ、ハシバミ、アーモンド、ピスタチオ、カシューナッツ、マカダミアナッツ等)、液果類(ブルーベリー、クランベリー、ブラックベリー、ラズベリー等)、ブドウ、カキ、オリーブ、ビワ、バナナ、コーヒー、ナツメヤシ、ココヤシ等、
果樹以外の樹;チャ、クワ等。
本発明によれば、作物の種子又は果実の数又は重量を増収することが可能となる。
化合物(1)を5部、化合物(A)5部、ホワイトカーボンとポリオキシエチレンアルキルエーテルサルフェートアンモニウム塩との混合物(重量割合1:1)35部及び水55部を混合し、湿式粉砕法で微粉砕することにより各フロアブル製剤を得る。
化合物(1)を10部、化合物(A)5部、ソルビタントリオレエ−ト1.5部、及びポリビニルアルコ−ル2部を含む水溶液28部を混合し、湿式粉砕法で微粉砕した後、この中にキサンタンガム0.05部及びアルミニウムマグネシウムシリケ−ト0.1部を含む水溶液45.50部を加え、さらにプロピレングリコ−ル10部を加えて攪拌混合しフロアブル製剤を得る。
化合物(1)10部、化合物(A)40部、リグニンスルホン酸カルシウム3部、ラウリル硫酸ナトリウム2部及び合成含水酸化珪素45部をよく粉砕混合することにより各水和剤を得る。
2010年9月3日、ナタネ種子を3.5kg/ヘクタールの密度で播種し、育てた。化合物(1)の25%フロワブル製剤及びテブコナゾール(:Horizon(登録商標)25%EW)を水で希釈し、化合物(1)及びテブコナゾールがそれぞれ150g/ヘクタールとなるように混合組成物を調整した。2011年5月19日、開花盛期(生育ステージBBCH65(Biologische Bundesanstalt Bundessortenamt and Chemical industry(BBCHスケール)))のナタネに、前記組成物を茎葉処理した。処理量は200L/ヘクタールとした。試験面積は3×8mとし、上記操作にて薬剤処理をした試験区を処理区とした。また、同じ試験面積の薬剤処理をしない試験区を無処理区とした。2011年8月9日、ナタネ種子を収穫し、1ヘクタールあたりの収量を調査した。調査対象のナタネ種子水分含量は9%とした。結果、処理区では4.3トン/ヘクタールの収量が得られたのに対し、無処理区では3.8トン/ヘクタールであった。試験期間中は、収量に影響し得る病害虫の発生は認められなかった。
Claims (8)
- 群(A)から選ばれる少なくとも1種の化合物が、テブコナゾール、プロチオコナゾール、シプロコナゾールまたはメトコナゾールである、請求項1に記載の増収方法。
- 群(A)から選ばれる少なくとも1種の化合物が、ボスカリド、フルオピラム、またはフルキサピロキサドである、請求項1に記載の増収方法。
- 群(A)から選ばれる少なくとも1種の化合物が、アゾキシストロビン、ジモキシストロビン、ピラクロストロビン、トリフロキシストロビンまたはピコキシストロビンである、請求項1に記載の増収方法。
- 式(1)で示される化合物と、群(A)から選ばれる少なくとも1種の化合物との重量比が、式(1)で示される化合物/群(A)から選ばれる化合物=0.0125/1~500/1である請求項1に記載の増収方法。
- 式(1)で示される化合物が、Rの絶対立体配置を有する、請求項1に記載の増収方法。
- 作物が、ナタネ、イネ、トウモロコシ、コムギ、オオムギ、インゲンマメ、ダイズ、モモ、リンゴ、またはセイヨウナシである請求項1に記載の増収方法。
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CN201380066096.5A CN104869825B (zh) | 2012-12-21 | 2013-12-13 | 作物的种子或果实的数目或重量的增收方法 |
US14/651,035 US10485233B2 (en) | 2012-12-21 | 2013-12-13 | Method for increasing yield of crop seeds or fruits in number or weight |
AU2013364884A AU2013364884B2 (en) | 2012-12-21 | 2013-12-13 | Method for increasing number or weight of crop seeds or fruits |
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WO2017026526A1 (ja) * | 2015-08-11 | 2017-02-16 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
WO2017153200A1 (en) | 2016-03-10 | 2017-09-14 | Basf Se | Fungicidal mixtures iii comprising strobilurin-type fungicides |
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WO2017178407A1 (en) * | 2016-04-13 | 2017-10-19 | Bayer Cropscience Aktiengesellschaft | Fungicidal combinations |
CN106342530A (zh) * | 2016-08-30 | 2017-01-25 | 铜陵翔宇商贸有限公司 | 一种芜菁高产种植方法 |
CN106922674A (zh) * | 2017-04-20 | 2017-07-07 | 深圳诺普信农化股份有限公司 | 一种杀菌组合物及其应用 |
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- 2013-12-13 CN CN201380066096.5A patent/CN104869825B/zh active Active
- 2013-12-13 EP EP13864993.4A patent/EP2936981B1/en active Active
- 2013-12-13 BR BR112015013967A patent/BR112015013967A2/pt not_active Application Discontinuation
- 2013-12-13 WO PCT/JP2013/084172 patent/WO2014098201A1/ja active Application Filing
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WO2017026526A1 (ja) * | 2015-08-11 | 2017-02-16 | 住友化学株式会社 | 植物病害防除組成物及び植物病害防除方法 |
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WO2017153200A1 (en) | 2016-03-10 | 2017-09-14 | Basf Se | Fungicidal mixtures iii comprising strobilurin-type fungicides |
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Publication number | Publication date |
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US10485233B2 (en) | 2019-11-26 |
PL2936981T3 (pl) | 2019-06-28 |
AU2013364884A1 (en) | 2015-06-18 |
CN104869825B (zh) | 2017-03-15 |
CA2893827A1 (en) | 2014-06-26 |
EP2936981B1 (en) | 2019-02-06 |
US20150313218A1 (en) | 2015-11-05 |
EP2936981A1 (en) | 2015-10-28 |
AU2013364884B2 (en) | 2017-07-06 |
CN104869825A (zh) | 2015-08-26 |
EP2936981A4 (en) | 2016-09-21 |
BR112015013967A2 (pt) | 2017-07-11 |
CA2893827C (en) | 2021-07-06 |
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