JP4599943B2 - Whitefly control agent - Google Patents
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- JP4599943B2 JP4599943B2 JP2004248003A JP2004248003A JP4599943B2 JP 4599943 B2 JP4599943 B2 JP 4599943B2 JP 2004248003 A JP2004248003 A JP 2004248003A JP 2004248003 A JP2004248003 A JP 2004248003A JP 4599943 B2 JP4599943 B2 JP 4599943B2
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Description
本発明は、コナジラミ類防除剤等に関する。 The present invention relates to whitefly control agents and the like.
従来、コナジラミ類等の防除を目的として、種々の殺虫剤が使用されている。 Conventionally, various insecticides have been used for the purpose of controlling whiteflies and the like.
しかしながら、コナジラミ類は殺虫剤に対して抵抗性を発達させ易く、そのため、これら殺虫剤が有する防除効果を低下させることになる。よって、あらゆる場面や状況においても殺虫剤のローテーションを可能とするように多種類の殺虫剤が用意されていることが好ましい。そして用意される殺虫剤の中でも、できるだけコナジラミ類における殺虫剤抵抗性の発達を遅らせることが可能となり、優れた防除効果を有するコナジラミ類防除剤の開発が求められている。 However, whiteflies tend to develop resistance to insecticides, thus reducing the control effect of these insecticides. Therefore, it is preferable that various types of insecticides are prepared so that the rotation of the insecticides is possible in every scene and situation. Among the insecticides prepared, it is possible to delay the development of insecticide resistance in whiteflies as much as possible, and the development of whiteflies control agents having an excellent control effect has been demanded.
かかる状況下、本発明者らは、種々のコナジラミ防除剤について検討した結果、澱粉と、(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オンとを組み合わせることによって、コナジラミ類に対して相乗効果を伴うような優れた防除効果を示すことを見出し、本発明を完成した。
即ち、本発明は、
1.有効成分として、澱粉(以下、物質Aと記すこともある。)と、(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オン(以下、物質Bと記すこともある。)とを含有することを特徴とするコナジラミ類防除剤(以下、本発明防除剤と記すこともある。);
2.澱粉と、(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オンとの混合重量比が、5:1〜50:1の割合で含有されることを特徴とする前項1記載のコナジラミ類防除剤;
3.コナジラミ類における殺虫剤抵抗性の発達を遅らせるためのローテーション用薬剤の有効成分としての、澱粉及び(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オンの使用;
4.インテグレイテッド ペスト マネジメント(Integrated Pest Management)における適用剤の有効成分としての、澱粉及び(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オンの使用;
等を提供するものである。
Under such circumstances, the present inventors have examined various whitefly control agents, and as a result, starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2 , 4-triazin-3 (2H) -one was found to exhibit an excellent control effect with a synergistic effect on whiteflies, and the present invention was completed.
That is, the present invention
1. As an active ingredient, starch (hereinafter sometimes referred to as substance A) and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4-triazine -3 (2H) -one (hereinafter also referred to as “substance B”), a whitefly control agent (hereinafter also referred to as “the present control agent”);
2. The mixing weight ratio of starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4-triazin-3 (2H) -one is 5: The whitefly control agent according to the preceding item 1, which is contained in a ratio of 1 to 50: 1;
3. Starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1, an active ingredient of a rotation agent for delaying the development of insecticide resistance in whiteflies Use of 2,4-triazin-3 (2H) -one;
4). Starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4- as active ingredients of application agents in Integrated Pest Management Use of triazin-3 (2H) -one;
Etc. are provided.
本発明により、コナジラミ類に対して優れた防除効果を有する防除剤を提供することが可能となった。 By this invention, it became possible to provide the control agent which has the control effect outstanding with respect to whitefly.
本発明防除剤の有効成分として含有される「澱粉」(即ち、物質A)は、馬鈴薯、甘薯、キャッサバ、小麦、トウモロコシ、米等から得られる天然の澱粉のみならず、これに加水分解、酸化等の処理が施された加工澱粉、アセチル化、メチル化等のアルキル化、ヒドロキシプロピル化等のヒドロキシアルキル化、アリル化、カルボキシメチル化等の処理が施された澱粉誘導体をも含む広い範囲の澱粉類を意味するものである。加工澱粉及び澱粉誘導体としては、具体的には例えば、デキストリン、アルファー化澱粉、アミロース、アミロペクチン、酸化澱粉、クラフト化澱粉、アルファー化ヒドロキシプロピル澱粉等を挙げることができる。また農薬として市販されているものとしては、例えば、SHIBUYA INDEX (Index of Pesticides) 9th Edition (2002) SHIBUYA INDEX RESEARCH GROUP 第85-14等に記載されている「粘着くん(商品名)」(住友化学工業)が挙げられる。 “Starch” (ie, substance A) contained as an active ingredient of the control agent of the present invention is not only natural starch obtained from potato, sweet potato, cassava, wheat, corn, rice, etc., but also hydrolyzed and oxidized A wide range of processed starches that have been treated, such as acetylated, methylated, etc. alkylated, hydroxypropylated, etc., hydroxyalkylated, allylated, carboxymethylated, etc. It means starches. Specific examples of the modified starch and starch derivative include dextrin, pregelatinized starch, amylose, amylopectin, oxidized starch, krafted starch, and pregelatinized hydroxypropyl starch. Examples of commercially available pesticides include “Adhesion-kun (trade name)” (Sumitomo Chemical Co., Ltd.) described in SHIBUYA INDEX (Index of Pesticides) 9th Edition (2002) SHIBUYA INDEX RESEARCH GROUP 85-14. Industrial).
本発明防除剤の有効成分として含有される「(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オン」(即ち、物質B)は、一般名ピメトロジン(pymetrozine)として知られている化合物であり、例えば、SHIBUYA INDEX (Index of Pesticides) 9th Edition (2002) SHIBUYA INDEX RESEARCH GROUP 第64-5等に記載されている「チェス(商品名)」(シンジェンタ)の有効成分である。 “(E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4-triazin-3 (2H) -one contained as an active ingredient of the control agent of the present invention (Ie, substance B) is a compound known by the general name pymetrozine, and is described, for example, in SHIBUYA INDEX (Index of Pesticides) 9th Edition (2002) SHIBUYA INDEX RESEARCH GROUP 64-5. It is an active ingredient of “chess (trade name)” (syngenta).
本発明防除剤は、その殺虫作用性からコナジラミ類における殺虫剤抵抗性の発達がないと考えられている物質Aを含み、かつ、このような物質Aと他有効成分である物質Bとの2種類の異なる殺虫作用性を同時に有することから、コナジラミ類における殺虫剤抵抗性の発達を十分に遅らせることが可能であり、このような防除剤をコナジラミ類防除のためのローテーション用薬剤として用いれば、当該防除剤だけではなく他のコナジラミ類防除剤における殺虫剤抵抗性の発達をも遅らせることが可能となる。 The control agent of the present invention contains a substance A which is considered to have no insecticide-resistant development in whiteflies due to its insecticidal activity, and 2 of such substance A and substance B which is another active ingredient. Since it has different insecticidal activity of different types, it is possible to sufficiently delay the development of insecticide resistance in whiteflies, and if such a control agent is used as a rotation agent for controlling whiteflies, It becomes possible to delay the development of insecticide resistance not only in the control agent but also in other whitefly control agents.
また、本発明防除剤は、天敵生物に対して害を与えにくい又は影響を及ぼさない等の特徴を有することから、複数の害虫防除法等を合理的に組み合わせ、経済的な視点から、害虫の密度や作物被害の変動等を見きわめながら防除の要否を判断する技術として最近注目されている、インテグレイテッド ペスト マネジメント(Integrated Pest Management)における適用剤として利用可能であり、このような適用剤の有効成分として、澱粉及び(E)−4,5−ジヒドロ−6−メチル−4−(3−ピリジルメチレンアミノ)−1,2,4−トリアジン−3(2H)−オンを使用してもよい。 In addition, since the control agent of the present invention has characteristics such as hardly causing harm to natural enemy organisms or having no effect, a plurality of pest control methods are rationally combined, and from an economical viewpoint, It can be used as an applied agent in Integrated Pest Management, which has recently been attracting attention as a technology for determining the necessity of control while observing changes in density and crop damage, etc. As ingredients, starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4-triazin-3 (2H) -one may be used.
本発明防除剤において防除の対象であるコナジラミ類としては、例えば、シルバーリーフコナジラミ、オンシツコナジラミ、タバココナジラミ等を挙げることができる。また本発明防除剤が施用される農園芸用植物としては、例えば、トマト、ナス及びピーマン等の蔬菜類、ポインセチア、バラ及びガーベラ等の花卉・花木類、かんきつ等の果樹類等が挙げられる。 Examples of whiteflies that are targets for control in the present control agent include silver leaf whitefly, on-site whitefly, tobacco whitefly, and the like. Examples of the agricultural and horticultural plants to which the control agent of the present invention is applied include sugar beet such as tomato, eggplant and bell pepper, flower buds and flower trees such as poinsettia, rose and gerbera, and fruit trees such as citrus.
本発明防除剤の有効成分として含有される物質A及び物質Bは、他の何らの成分も加えず、そのまま使用してもよいが、通常、固体担体、液体担体等の各種担体と混合し、必要によって添加剤として界面活性剤、その他の製剤用補助剤を加えて、水和剤、顆粒状水和剤、乳剤、水溶剤、液剤、水中懸濁剤、水中乳濁剤等のフロアブル剤、粉剤等の製剤にして使用するか、又は、それぞれの有効成分を上記のような各種剤型に製剤した後混合するか、又は、さらに水で希釈してそれぞれの薬液に調製した後に混合することもできる。これらの製剤には、有効成分として物質Aと物質Bとの混合重量比が、通常、5:1〜50:1の割合で含有され、製剤中の全有効成分量は、重量比で、通常、0.1%〜95%である。
上記のような製剤の際に用いられる固体担体としては、例えば、クレー、タルク、ベントナイト、酸性白土、珪藻土、炭酸カルシウム、ゼオライト、澱粉、デキストリン、ホワイトカーボン、硫酸アンモニウム、硫酸ナトリウム及び塩化カリウム等を挙げることができ、液体担体としては、例えば、水、エタノール、イソプロパノール、ブタノール等の炭素数1〜8のモノアルコール、エチレングリコール、プロピレングリコール、ジエチレングリコール、ヘキシレングリコール等の炭素数2〜8のジオール等を挙げることができる。界面活性剤としては、例えば、公知の陰イオン界面活性剤、非イオン界面活性剤、陽イオン界面活性剤、両性界面活性剤が挙げられる。その他の製剤用補助剤としては、例えば、乳化剤、安定剤、分散剤、湿潤剤、懸濁化剤、展着剤、浸透剤、防菌防黴剤等を挙げることができ、具体的には例えば、カゼイン、ゼラチン、多糖類、リグニン誘導体、ベントナイト、糖類、合成水溶性高分子、PAP(酸性リン酸イソプロピル)、BHT(2,6-ジ-tert-ブチル-4-メチルフェノール)、BHA(2-/3-tert-ブチル-4-メトキシフェノール)、植物油、鉱物油、界面活性剤、脂肪酸又はそのエステル等が挙げられる。
Substance A and substance B contained as active ingredients of the control agent of the present invention may be used as they are without adding any other components, but usually mixed with various carriers such as a solid carrier and a liquid carrier, If necessary, surfactants and other formulation adjuvants are added as additives, and flowable agents such as wettable powder, granular wettable powder, emulsion, aqueous solvent, liquid, suspension in water, emulsion in water, Use as a preparation such as powder, or mix each active ingredient after formulating it into various dosage forms as described above, or mix it after further diluting with water to prepare each drug solution. You can also. In these preparations, the mixing weight ratio of substance A and substance B as active ingredients is usually contained in a ratio of 5: 1 to 50: 1, and the total amount of active ingredients in the preparation is usually in a weight ratio. 0.1% to 95%.
Examples of the solid carrier used in the preparation as described above include clay, talc, bentonite, acid clay, diatomaceous earth, calcium carbonate, zeolite, starch, dextrin, white carbon, ammonium sulfate, sodium sulfate and potassium chloride. Examples of liquid carriers include monoalcohols having 1 to 8 carbon atoms such as water, ethanol, isopropanol and butanol, diols having 2 to 8 carbon atoms such as ethylene glycol, propylene glycol, diethylene glycol and hexylene glycol. Can be mentioned. Examples of the surfactant include known anionic surfactants, nonionic surfactants, cationic surfactants, and amphoteric surfactants. Examples of other formulation adjuvants include emulsifiers, stabilizers, dispersants, wetting agents, suspending agents, spreading agents, penetrating agents, antifungal agents, and the like. For example, casein, gelatin, polysaccharides, lignin derivatives, bentonite, saccharides, synthetic water-soluble polymers, PAP (isopropyl acid phosphate), BHT (2,6-di-tert-butyl-4-methylphenol), BHA ( 2- / 3-tert-butyl-4-methoxyphenol), vegetable oils, mineral oils, surfactants, fatty acids or esters thereof.
このようにして得られる製剤は、通常、前記のような水溶剤、水和剤、顆粒状水和剤、乳剤、液剤等の製剤を水等により希釈された希釈液の形態で施用される。
本発明防除剤の施用濃度は、物質Aの濃度として、コナジラミ類防除に有効な量であって、通常、100ppm〜1000ppmであり、好ましくは200ppm〜800ppmである。また物質Bの濃度として、通常、30ppm〜200ppmであり、好ましくは50ppm〜100ppmである。
本発明防除剤の施用量は、施用場所10アール当たり、物質Aの量に換算して、通常、10g〜700g、好ましくは20g〜560gであり、物質Bの量に換算して、通常、3g〜140g、好ましくは5g〜30gである。
尚、これらの施用濃度及び施用量は、いずれも製剤の種類、施用時期、施用場所、施用方法、コナジラミ類の種類、被害程度等の状況によって異なり、上記の範囲にかかわることなく増加させたり、減少させたりすることができる。
The preparation thus obtained is usually applied in the form of a diluted solution obtained by diluting a preparation such as the above-mentioned aqueous solvent, wettable powder, granular wettable powder, emulsion, and liquid with water or the like.
The application concentration of the control agent of the present invention is an amount effective for controlling whitefly as the concentration of the substance A, and is usually 100 ppm to 1000 ppm, preferably 200 ppm to 800 ppm. Further, the concentration of the substance B is usually 30 ppm to 200 ppm, preferably 50 ppm to 100 ppm.
The application amount of the control agent of the present invention is usually 10 g to 700 g, preferably 20 g to 560 g in terms of the amount of substance A per 10 ares of application site, and usually 3 g in terms of the amount of substance B. ~ 140g, preferably 5g ~ 30g.
These application concentrations and application rates vary depending on the type of preparation, application time, application location, application method, type of whiteflies, damage level, etc., and can be increased regardless of the above range, It can be reduced.
次に、本発明を実施例及び試験例により、更に具体的に説明するが、本発明はこれらに限定されるものではない。以下の説明において「部」は重量部を表す。 EXAMPLES Next, although an Example and a test example demonstrate this invention further more concretely, this invention is not limited to these. In the following description, “parts” represents parts by weight.
製剤例1
トクシールGUN(徳山曹達製ホワイトカーボン)5部、物質Aとしてマツノリン500(松谷化学工業製澱粉)40部、物質Bとしてピメトロジン8部、ソルポール5060(アルキルベンゼンスルホン酸ナトリウム、東邦化学製界面活性剤)5部及び勝光山クレー(勝光山鉱業所製クレー)42部を粉砕混合することによって、本発明防除剤(水和剤)を得た。
Formulation Example 1
5 parts of Toxeal GUN (white carbon manufactured by Tokuyama Soda), 40 parts of matsunoline 500 (starch made by Matsutani Chemical Industry) as substance A, 8 parts of pymetrozine as substance B, 5 solpol 5060 (sodium alkylbenzenesulfonate, surfactant manufactured by Toho Chemical) 5 The present control agent (wetting agent) was obtained by pulverizing and mixing 42 parts of Katsumiyama clay and 42 parts of Katsumiyama clay (Clay made by Katsuyama mining company).
試験例1
液剤として製剤された物質A(住友化学工業、粘着くん5%液剤)と、水和剤として製剤された物質B(シンジェンタジャパン、チェス25%水和剤)とを各々水で希釈し、当該希釈液を所定の有効成分濃度になるように混合することによって、供試薬剤を得た。
一方、縦15cm×横15cm×高さ30cmの枠にテトロンゴースを張り、枠内にポット植えトマトを置き、オンシツコナジラミ成虫を30頭放飼した。24時間静置した後、上記の供試薬剤をハンドスプレイヤーでトマトに充分量散布し、散布24時間後に死虫率を調査した。試験は3反復で行った。
尚、混合前の各々の希釈液を、後述の理論値殺虫率を算出するための対照防除剤として同様に試験した。
その結果を表1に示す。尚、理論値殺虫率(%)は下記の式により算出した。
Test example 1
Substance A (Sumitomo Chemical Co., Ltd., Adhesive-kun 5% solution) formulated as a liquid and Substance B (Syngenta Japan, Chess 25% wettable powder) formulated as a wettable powder are each diluted with water. The reagent was obtained by mixing the liquid so as to have a predetermined active ingredient concentration.
On the other hand, Tetorongose was put on a frame of 15 cm in length × 15 cm in width × 30 cm in height, pot-planted tomatoes were placed in the frame, and 30 adult white lice were released. After leaving still for 24 hours, a sufficient amount of the above-mentioned reagent supply was sprayed on tomatoes with a hand sprayer, and the death rate was investigated 24 hours after spraying. The test was performed in triplicate.
In addition, each diluted solution before mixing was similarly tested as a control agent for calculating a theoretical insecticidal rate described later.
The results are shown in Table 1. The theoretical value insecticidal rate (%) was calculated by the following formula.
理論値殺虫率(%)=a+{(100−a)×b}/100
ここでaは物質Aの殺虫率(%)を表し、bは物質Bの殺虫率(%)を表す。
Theoretical insecticidal rate (%) = a + {(100−a) × b} / 100
Here, a represents the insecticidal rate (%) of the substance A, and b represents the insecticidal rate (%) of the substance B.
本発明により、コナジラミ類に対して優れた防除効果を有する防除剤を提供することが可能となった。
By this invention, it became possible to provide the control agent which has the control effect outstanding with respect to whitefly.
Claims (4)
Starch and (E) -4,5-dihydro-6-methyl-4- (3-pyridylmethyleneamino) -1,2,4- as active ingredients of application agents in Integrated Pest Management Use of triazin-3 (2H) -one.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004248003A JP4599943B2 (en) | 2004-08-27 | 2004-08-27 | Whitefly control agent |
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| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2004248003A JP4599943B2 (en) | 2004-08-27 | 2004-08-27 | Whitefly control agent |
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| Publication Number | Publication Date |
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| JP2006063022A JP2006063022A (en) | 2006-03-09 |
| JP4599943B2 true JP4599943B2 (en) | 2010-12-15 |
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| JP2004248003A Expired - Fee Related JP4599943B2 (en) | 2004-08-27 | 2004-08-27 | Whitefly control agent |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| MY121190A (en) * | 1992-09-10 | 2006-01-28 | Syngenta Participations Ag | Control of pests using 1,2,4-triazine derivatives. |
| JP3512854B2 (en) * | 1993-09-10 | 2004-03-31 | 住友化学工業株式会社 | Pest control agent and pest control method |
| JPH11343201A (en) * | 1998-04-03 | 1999-12-14 | Agurosu:Kk | Pest control composition |
| JP4543503B2 (en) * | 2000-04-25 | 2010-09-15 | 住友化学株式会社 | Insecticide / miticide and insecticide / miticide method |
| JP2002332205A (en) * | 2001-05-09 | 2002-11-22 | Sumitomo Chem Co Ltd | Insecticide and acaricide and insecticide and acaricide method |
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