JPS6340405B2 - - Google Patents

Info

Publication number
JPS6340405B2
JPS6340405B2 JP56051843A JP5184381A JPS6340405B2 JP S6340405 B2 JPS6340405 B2 JP S6340405B2 JP 56051843 A JP56051843 A JP 56051843A JP 5184381 A JP5184381 A JP 5184381A JP S6340405 B2 JPS6340405 B2 JP S6340405B2
Authority
JP
Japan
Prior art keywords
parts
days later
moth
days
compound
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
JP56051843A
Other languages
Japanese (ja)
Other versions
JPS57167906A (en
Inventor
Shizuo Wakita
Horan Jooji
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Kayaku Co Ltd
Original Assignee
Nippon Kayaku Co Ltd
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 Nippon Kayaku Co Ltd filed Critical Nippon Kayaku Co Ltd
Priority to JP56051843A priority Critical patent/JPS57167906A/en
Publication of JPS57167906A publication Critical patent/JPS57167906A/en
Publication of JPS6340405B2 publication Critical patent/JPS6340405B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は3′―フエノキシ―α―シアノベンジル
―1―(4―エトキシフエニル)―2、2―ジク
ロロシクロプロパンカルボキシレート(以下「化
合物A」と略称する。)と2―クロロ―1―(2、
4―ジクロロフエニル)ビニルジメチルホスフエ
ート(以下、「ジメチルビンホス」と略称する。)、
0、0―ジメチル―0―(3、5、6―トリクロ
ロ―2―ピリジル)ホスホロチオエート(以下、
「クロルピリホスメチル」と略称する。)0、0―
ジエチル―0―(5―フエニル―3―イソキサゾ
リル)ホスホロチオエート(以下、「イソキサチ
オン」と略称する。)および0、0―ジエチル―
0―(3―オキソ―2―フエニル―2H―ピリダ
ジン―6―イル)ホスホロチオエート(以下、
「ピリダフエンチオン」と略称する。)からなる群
から選ばれた少くとも1種以上の化合物を有効成
分として含有することを特徴とする殺虫組成物に
関するものである。 今日、農園芸用害虫、森林害虫あるいは衛生害
虫等の各種害虫の防除を目的とする度重なる薬剤
散布の結果、各害虫とも薬剤感受性の低下した系
統が各地で出現し、その防除が一層困難になつて
きたため、防除技術上または農家経営上の大きな
問題点となつている。 したがつて、これら害虫特に、薬剤感受性の低
下した系統に対して顕著な薬剤抵抗性害虫殺虫効
力を示し、薬剤散布に際し、その回数、薬量を軽
減し、かつ人畜への安全性が高く、かつ環境汚染
の少ない防除薬剤の出現が強く望まれている。 本発明者等は鋭意研究の結果、化合物Aとジメ
チルビンホス、クロルピリホスメチル、イソキサ
チオンおよびピリダフエンチオンからなる群から
選ばれた少くとも1種以上の化合物を有効成分と
する組成物が農園芸用害虫や他の森林害虫あるい
は衛生害虫等に対して確実な防除効果を有するこ
とを見出し、これに基づいてさらに研究を進めた
結果、この発明を完成した。 本発明殺虫組成物は薬剤抵抗性害虫殺虫効力お
よび速効的殺虫効力並びに持続的殺虫効力の点に
おいて、各単剤の効力からは推定出来ない驚くべ
き防除効果―すなわち単剤の特徴的性質が単に相
加されたものではなく顕著な相乗的な作用効果を
示すものである。 その結果、より確実な防除効果が得られ、薬剤
の散布回数を軽減し、かつ散布量が通常各々の単
剤で散布する薬剤量の約1/2に減少でき、薬剤
散布時の安全性と人畜への安全性を高め、環境汚
染を少くすることが出来る。 本発明組成物の適用害虫は、ニカメイチユウ、
コブノメイガ、モンシロチヨウ等の他にイエバ
エ、チヤバネゴキブリ、ヤマトゴキブリ、クロゴ
キブリ、ワモンゴキブリ、アカイエカ、チカイエ
カ、ネツタイシマカ、コクゾウムシ、ヒラタコク
ヌストモドキ、ハイマダラノメイガ、アズキゾウ
ムシ、ツマグロヨコバイ、セジロウンカ、ヒメト
ビウンカ、トビイロウンカ、ニカメイチユウ、イ
チモンジセセリ、イネハモグリバエ、イネヒメハ
モグリバエ、イネカラバエ、イネクビホソハム
シ、イネミズゾウムシ、イネゾウムシ、コナガ、
ヨトウ、ハスモンヨトウ、ナカジロシタバ、アワ
ノメイガ、マメシンクイガ、シロイチモンジマダ
ラメイガ、マメヒメサヤムシガ、モモアカアブラ
ムシ、ワタアブラムシ、ニセダイコンアブラム
シ、ミカンクロアブラムシ、バラヒゲナガアブラ
ムシ、オンシツコナジラミ、アメリカシロヒト
リ、マイマイガ、マツカレハ、コカクモンハマ
キ、ナシヒメシンクイムシ、モモシンクイムシ、
キンモンホソガ、ミカンハモグリガ、チヤノキイ
ロアザミウマ、コアオハナムグリ、ゴマダラカミ
キリ、シバツトガ、スジキリヨトウ等の諸害虫に
も適用することが出来る。 本発明の上記組成物を使用する場合、使用目的
に応じて、そのまま直接水で希釈して使用する
か、または農薬補助剤を用いて、農薬製剤分野に
おいて一般に行われている方法により乳剤、水和
剤、粉剤、粒剤、エアロゾル、フロアブル剤、高
濃度微量散布剤等の製剤形態にして使用すること
ができる。これら各種製剤は実際の使用に際して
は、直接そのまま使用するか、または水で所望濃
度に希釈して使用することができる。 ここにいう農薬補助剤は不活性溶剤および/ま
たは担体(希釈剤)を、さらに種々の界面活性剤
および/または有機質原料等をあげることができ
る。溶剤としては、灯油、軽油等の石油分溜物、
トルエン、キシレン等の芳香族炭化水素、メチル
ナフタレン、シクロヘキサン、メタノール、ブタ
ノール、グリコール等のアルコール、アセトン、
ジメチルホルムアミド等のアミド類、ジメチルス
ルホキシド等のスルホキシド類、動植物油、脂肪
酸、脂肪酸エステル等があげられる。 担体(希釈剤)としては、クレー、カオリン、
タルク、珪藻土、シリカ、炭酸カルシウム、モン
モリロナイト、ベントナイト、長石、石英、アル
ミナ等があげられる。 界面活性剤としては、たとえば高級アルコール
硫酸ナトリウム、ステアリルトリメチルアンモニ
ウムクロライド、ポリオキシエチレンアルキルフ
エニルエーテル、ラウリルベタイン等の陰イオン
系界面活性剤、陽イオン系界面活性剤、非イオン
系界面活性剤、両性イオン系界面活性剤があげら
れる。 また農薬に通常使用される担体以外の補助剤た
とえば展着剤、乳化剤、湿展剤、分散剤、固着
剤、崩壊剤等を必要に応じ適当に混合して殺虫効
果を確実にすることが出来る。 本発明の殺虫組成物は製剤における化合物Aと
各有機リン系殺虫剤の混合物の濃度を0.5〜95%
(重量)、好ましくは1.5〜80%(重量)の範囲で
含有することが出来る。 化合物Aと各有機リン系殺虫剤との配合割合
は、化合物Aの1重量部に対し有機リン系殺虫剤
を1.0〜5.0重量部、好ましくは2.0〜4.0重量部の
範囲で含有することが出来る。 本発明の組成物の使用量は剤形、施用する方
法、時期、その他の条件によつて変るが、通常10
アール当り有効成分量で20〜300g、好ましくは
30〜250gが使用される。たとえば粉剤は10アー
ル当り有効成分で30〜120g、粒剤は有効成分で
120〜240g、また乳剤、水和剤は有効成分で40〜
250gの範囲である。しかしながら特別の場合に
は、これらの範囲を超えることが、または下まわ
ることが可能であり、また時には必要でさえあ
る。いずれの製剤もそのまま単独で使用出来るの
みならず殺菌剤、除草剤、植物生長調節剤、農園
芸用殺菌剤、土壌殺菌剤、土壌改良剤、殺線虫
剤、あるいは殺ダニ剤と混合しても良く、さらに
肥料中他の殺虫剤と混合しても良い。 次に本発明の製剤例について以下の実施例でさ
らに詳細に説明するが、添加物の種類および混合
比率はこれらのみに限定されることなく広い範囲
で使用可能である。なお部とあるのは「重量部」
を意味する。 実施例 1 乳 剤 化合物A10部とイソキサチオン30部にキシレン
―メチルナフタレンの混合液(1:1)45部を加
え溶解し、次いでこれにアルキルフエノール酸化
エチレン縮合物とアルキルベンゼンスルホン酸カ
ルシウムの混合物(8:2)15部を加えて乳剤と
する。 本剤は1000〜4000倍に水で希釈し、散布液とし
て使用する。 実施例 2 水和剤 化合物A20部とクロルピリホスメチル20部に合
成珪酸微粉末52.5部に混合し、さらにラウリン酸
ナトリウムとジナフチルメタンスルホン酸ナトリ
ウムの混合物(1:1)7.5部を混合して微粉砕
して粉剤を得る。 本剤は1000〜4000倍に水で希釈して水和剤とし
て散布液として使用する。 実施例 3 粉 剤 化合物A1部とピリダフエンチオン2部にタル
クと炭酸カルシウムの混合物(1:1)95部を加
え、混合磨砕して充分均等に分散配合した後、さ
らに合成珪酸微粉末2部を添加し、混合粉砕し粉
剤とする。本剤はこのまま散布して使用する。 実施例 4 粒 剤 化合物A2.5部とジメチルビンホス2.5部をベン
トナイト微粉末47部、タルク46部、リグニンスル
ホン酸ナトリウム2部と混合した後、水を加え均
等になるまで混練する。 次に射出成型機を通して造粒し、整粒機、乾燥
機、篩を通すことにより粒径0.6〜1.0mmの粒剤と
する。本剤は直接水田面および土壌面に散粒して
使用する。 以下に述べるごとく種々の実験例より明らかな
ように本発明殺虫組成物は、それぞれの単剤に比
較して優れた薬剤抵抗性害虫殺虫効力および速効
的殺虫効力並びに持続的殺虫効力を示し、また、
圃場試験においても勝れた防除効果を示すもので
ある。 実験例 1 ニカメイチユウ殺虫試験 稲品種ムサシモチを5本1株で1/10000アー
ルの鉢に植え、草丈30cmに達した時、その鉢をタ
ーンテーブルに乗せ、16r.p.mの速度で回転させ
る。距離1mよりコンプレツサースプレーガンに
て圧力1Kg/cm3で乳剤又は水和剤を水道水で所定
濃度に希釈した液を鉢に散布した。散布1日後、
3日後および7日後に岡山県金光町より採集し、
累代飼育中のニカメイチユウ孵化直後の幼虫15匹
をその鉢に放虫した。3日後すなわち、散布日か
ら4日後(以下「4日後」という。)、6日後(以
下「6日後」という。)および10日後(以下「10
日後」という。)の稲をとりだし、実体顕微鏡下
で稲を分解しそれぞれの日の死虫数を調査し、死
虫率を求めた。尚、実験はガラス温室中、1区3
連制で実施した。結果は表1に示す。
The present invention relates to 3'-phenoxy-α-cyanobenzyl-1-(4-ethoxyphenyl)-2,2-dichlorocyclopropanecarboxylate (hereinafter abbreviated as "Compound A") and 2-chloro-1- (2,
4-dichlorophenyl) vinyl dimethyl phosphate (hereinafter abbreviated as "dimethylvinphos"),
0,0-dimethyl-0-(3,5,6-trichloro-2-pyridyl)phosphorothioate (hereinafter referred to as
It is abbreviated as "chlorpyrifosmethyl." )0, 0-
Diethyl-0-(5-phenyl-3-isoxazolyl) phosphorothioate (hereinafter abbreviated as "isoxathion") and 0,0-diethyl-
0-(3-oxo-2-phenyl-2H-pyridazin-6-yl) phosphorothioate (hereinafter referred to as
It is abbreviated as "pyridafentione". ) The present invention relates to an insecticidal composition containing as an active ingredient at least one compound selected from the group consisting of: Today, as a result of repeated spraying of chemicals for the purpose of controlling various pests such as agricultural and horticultural pests, forest pests, and sanitary pests, strains of each pest with reduced chemical sensitivity have appeared in various places, making their control even more difficult. As it has become more common, it has become a major problem in terms of pest control technology and farm management. Therefore, it exhibits remarkable insecticidal efficacy against these insect pests, especially those with reduced drug susceptibility, and reduces the frequency and amount of chemical spraying, and is highly safe for humans and livestock. There is a strong desire for a pest control agent that causes less environmental pollution. As a result of intensive research, the present inventors have found that a composition containing as active ingredients Compound A and at least one compound selected from the group consisting of dimethylvinphos, chlorpyrifos-methyl, isoxathion, and pyridafenethione has been found. It was discovered that the present invention has a reliable control effect on agricultural pests, other forest pests, sanitary pests, etc. Based on this, further research was conducted, and as a result, this invention was completed. The insecticidal composition of the present invention has surprising control effects in terms of insecticidal efficacy, rapid insecticidal efficacy, and sustained insecticidal efficacy that cannot be estimated from the efficacy of each single agent. In other words, the characteristic properties of a single agent are simply It shows a significant synergistic effect rather than an additive effect. As a result, a more reliable pest control effect can be obtained, the number of times the chemical is sprayed can be reduced, and the amount of spraying can be reduced to approximately 1/2 of the amount normally sprayed with each single agent, improving safety when spraying the chemical. It can improve safety for humans and livestock and reduce environmental pollution. The pests to which the composition of the present invention is applied are
In addition to the brown borer moth, the Japanese cockroach, the Japanese cockroach, the black cockroach, the American cockroach, the Culex mosquito, the common mosquito, the Aedes aegypti mosquito, the black weevil, the Japanese black weevil, the white-spotted weevil, the red-spotted weevil, the black leafhopper, the white-legged planthopper, the brown planthopper, the brown planthopper, and the Japanese brown planthopper. , rice leafminer, rice leafminer, rice leafminer, rice leafminer, rice leaf beetle, rice water weevil, rice weevil, diamondback moth,
Spodoptera aphid, Spodoptera aphid, Japanese whitefly, corn borer moth, Japanese bean moth, white-spotted moth, Japanese bean aphid moth, green peach aphid, cotton aphid, false radish aphid, orange black aphid, rose bush aphid, Japanese whitefly, American white flycatcher, gypsy moth, pine kareha, white radish aphid , peach beetle, peach beetle,
It can also be applied to various pests such as the golden leaf moth, the orange leafminer moth, the Chinese yellow thrips, the red leaf beetle, the red leaf beetle, the white leaf moth, and the striped armyworm. When using the above-mentioned composition of the present invention, depending on the purpose of use, it may be diluted directly with water, or it may be made into an emulsion using a method commonly used in the field of agrochemical formulations, using an agrochemical adjuvant. It can be used in the form of preparations such as powders, powders, granules, aerosols, flowables, and high-concentration micro-dispersants. In actual use, these various preparations can be used directly or diluted with water to a desired concentration. The agrochemical auxiliaries mentioned herein include inert solvents and/or carriers (diluents), as well as various surfactants and/or organic raw materials. As a solvent, petroleum fractions such as kerosene and light oil,
Aromatic hydrocarbons such as toluene and xylene, alcohols such as methylnaphthalene, cyclohexane, methanol, butanol, and glycol, acetone,
Examples include amides such as dimethylformamide, sulfoxides such as dimethyl sulfoxide, animal and vegetable oils, fatty acids, fatty acid esters, and the like. As a carrier (diluent), clay, kaolin,
Examples include talc, diatomaceous earth, silica, calcium carbonate, montmorillonite, bentonite, feldspar, quartz, and alumina. Examples of the surfactant include anionic surfactants such as higher alcohol sodium sulfate, stearyltrimethylammonium chloride, polyoxyethylene alkyl phenyl ether, lauryl betaine, cationic surfactants, nonionic surfactants, Examples include zwitterionic surfactants. In addition, auxiliary agents other than carriers normally used for agricultural chemicals, such as spreading agents, emulsifiers, wetting agents, dispersants, fixing agents, disintegrants, etc., can be appropriately mixed as necessary to ensure the insecticidal effect. . In the insecticidal composition of the present invention, the concentration of the mixture of Compound A and each organophosphorus insecticide in the formulation is 0.5 to 95%.
(by weight), preferably in the range of 1.5 to 80% (by weight). The compounding ratio of Compound A and each organophosphorus insecticide is 1.0 to 5.0 parts by weight, preferably 2.0 to 4.0 parts by weight, per 1 part by weight of Compound A. . The amount of the composition of the present invention to be used varies depending on the dosage form, application method, timing, and other conditions, but is usually 10
20-300g of active ingredient per unit, preferably
30-250g is used. For example, powders have an active ingredient of 30 to 120g per 10ares, and granules have an active ingredient of 30 to 120g per 10ares.
120~240g, and emulsions and hydrating agents have active ingredients of 40~
It is in the range of 250g. However, in special cases it is possible, and sometimes even necessary, to exceed or fall below these ranges. All formulations can be used alone or mixed with fungicides, herbicides, plant growth regulators, agricultural and horticultural fungicides, soil fungicides, soil conditioners, nematicides, or acaricides. It can also be mixed with other insecticides in fertilizers. Next, formulation examples of the present invention will be explained in more detail in the following examples, but the types and mixing ratios of additives are not limited to these and can be used in a wide range. Note that "part" means "weight part"
means. Example 1 Emulsion 45 parts of a xylene-methylnaphthalene mixture (1:1) was added and dissolved in 10 parts of Compound A and 30 parts of isoxathion, and then a mixture of alkylphenol oxide ethylene condensate and calcium alkylbenzenesulfonate (8 parts) was added and dissolved. :2) Add 15 parts to make an emulsion. This agent is diluted 1000 to 4000 times with water and used as a spray solution. Example 2 Wettable powder 20 parts of Compound A and 20 parts of chlorpyrifos-methyl are mixed with 52.5 parts of synthetic silicic acid fine powder, and further mixed with 7.5 parts of a mixture of sodium laurate and dinaphthyl sodium methanesulfonate (1:1). Grind to obtain powder. This agent is diluted 1,000 to 4,000 times with water and used as a spray liquid as a hydrating agent. Example 3 Powder 95 parts of a mixture of talc and calcium carbonate (1:1) was added to 1 part of compound A and 2 parts of pyridafenethion, mixed and ground to sufficiently evenly disperse and blend, and then synthetic silicic acid fine powder was added. Add 2 parts and mix and crush to make a powder. This agent can be used as is by spraying. Example 4 Granules 2.5 parts of Compound A and 2.5 parts of dimethylvinphos are mixed with 47 parts of bentonite fine powder, 46 parts of talc, and 2 parts of sodium ligninsulfonate, and then water is added and kneaded until uniform. Next, the mixture is granulated using an injection molding machine, and then passed through a sieve, a dryer, and a sieve to form granules with a particle size of 0.6 to 1.0 mm. This agent is used by directly scattering it on the paddy field and soil surface. As is clear from various experimental examples as described below, the insecticidal composition of the present invention exhibits superior insecticidal efficacy, fast-acting insecticidal efficacy, and sustained insecticidal efficacy compared to each single agent, and also ,
It also shows excellent control effects in field tests. Experimental example 1 Insect killing test on Musashimochi rice plant Five plants of the rice variety Musashimochi were planted in a pot of 1/10000 are. When the plant reached a height of 30 cm, the pot was placed on a turntable and rotated at a speed of 16 rpm. An emulsion or a wettable powder diluted with tap water to a predetermined concentration was sprayed onto the pot at a pressure of 1 kg/cm 3 from a distance of 1 m using a compressor spray gun. One day after spraying,
Collected from Konko Town, Okayama Prefecture 3 and 7 days later,
Fifteen newly hatched larvae of N. japonica, which had been reared for generations, were released into the pot. 3 days later, that is, 4 days after the spraying date (hereinafter referred to as "4 days later"), 6 days later (hereinafter referred to as "6 days later"), and 10 days later (hereinafter referred to as "10 days later").
``Days later.'' ), the rice was disassembled under a stereomicroscope, and the number of dead insects on each day was investigated to determine the mortality rate. The experiment was conducted in the glass greenhouse, in Ward 1, Section 3.
It was carried out in tandem. The results are shown in Table 1.

【表】 実験例 2 コナガ殺虫試験 径9cmの鉢に移植したキヤベツ(品種:四委取
り甘らん)が本葉7〜8枚になつた時、その鉢を
ターンテーブル(16r.p.m)に乗せ距離1mよりコ
ンプレツサースプレーガンにて圧力1Kg/cm3で薬
液がしたたり落ちる程度に散布した。散布1日
後、7日後、14日後および21日後に埼玉県大宮市
より採集し累代飼育中のコナガ3令幼虫10匹をそ
の鉢に放虫した。1日後すなわち、散布日から2
日後(以下、「2日後」という。)、8日後(以下、
「8日後」という。)、15日後(以下、「15日後」と
いう。)および22日後(以下、「22日後」という。)
の生存虫数を調査した。 尚、実験は、ガラス温室内中1区3連制で実施
した。結果は表2に示す。
[Table] Experimental Example 2 Diamondback Moth Insect Killing Test When a cabbage (variety: Shikatori Amanan) transplanted into a 9 cm diameter pot had 7 to 8 true leaves, the pot was placed on a turntable (16 rpm). The chemical solution was sprayed from a distance of 1 m using a compressor spray gun at a pressure of 1 kg/cm 3 to the extent that it dripped. 1 day, 7 days, 14 days and 21 days after spraying, 10 3rd instar larvae of the diamondback moth collected from Omiya City, Saitama Prefecture and reared for generations were released into the pots. 1 day later, i.e. 2 days after the date of spraying
Days later (hereinafter referred to as “two days later”), Eight days later (hereinafter referred to as “two days later”),
It says "8 days later." ), 15 days later (hereinafter referred to as "15 days later") and 22 days later (hereinafter referred to as "22 days later").
The number of surviving insects was investigated. The experiment was conducted in three consecutive sessions in the first section of a glass greenhouse. The results are shown in Table 2.

【表】【table】

【表】 実験例 3 モンシロチヨウ防除試験(圃場) モンシロチヨウ圃場試験を埼玉県上尾市内のキ
ヤベツ畑で実施した。9月23日に移植したキヤベ
ツ(品種:四季取り甘ラン)畑を20m2に区割し、
10月21日に動力噴霧機で希釈薬液130/10aを
散布した。散布前ならびに散布後の1定期日(3
日後、7日後および14日後)に1区当り10株上の
モンシロチヨウの幼虫数を調査した。1区2連制
で実施した。 結果は表3に示す。
[Table] Experimental example 3. Prunus elegans control test (field) A field test of P. elegans was conducted in a cabbage field in Ageo City, Saitama Prefecture. The cabbage field (variety: Shiki Tori Amanran) that was transplanted on September 23rd was divided into 20m2 sections.
On October 21st, diluted chemical solution 130/10a was sprayed using a power sprayer. 1 regular day (3 days before and after spraying)
After 1 day, 7 days, and 14 days), the number of larvae of the cabbage on 10 plants per plot was investigated. It was carried out in two consecutive districts. The results are shown in Table 3.

【表】 実験例 4 コブノメイガ防除試験(圃場) コブノメイガ圃場試験を鹿児島県出水市内の一
般農家水田で実施した。稲品種コガネマサリ(田
植日6月20日)を裁培中の水田を125m2に区切り、
8月7日に各粉剤を4Kg/10a相当量を動力散粉
器で散布した。1区2連制で実施し、散布前なら
びに散布後15日に100株当りのコブノメイガ幼虫
の被害葉数を調査した。 結果は表4に示す。表中の補正被害指数は下記
の式より算出した。 補正被害指数=無処理区の処理前被害葉数×処理区の処
理後被害葉数/無処理区の処理後被害葉数×処理区の処
理前被害葉数×100
[Table] Experimental Example 4 Kobuno borer control test (field) A Kobuno borer moth field test was conducted in a general farmer's paddy field in Izumi City, Kagoshima Prefecture. A paddy field under cultivation of the rice variety Koganemasari (planting date: June 20th) was divided into 125 m2 sections.
On August 7th, an amount equivalent to 4 kg/10 a of each powder was spread using a power duster. The application was carried out in two consecutive sessions in one area, and the number of leaves damaged by the larvae of the Knot borer moth per 100 plants was investigated before and 15 days after the application. The results are shown in Table 4. The corrected damage index in the table was calculated using the following formula. Corrected damage index = Number of damaged leaves in untreated area before treatment × Number of damaged leaves in treated area after treatment / Number of damaged leaves in untreated area after treatment × Number of damaged leaves in treated area before treatment × 100

【表】【table】

Claims (1)

【特許請求の範囲】[Claims] 1 3′―フエノキシ―α―シアノベンジル―1―
(4―エトキシフエニル)―2、2―ジクロロシ
クロプロパンカルボキシレートと、2―クロロ―
1―(2、4―ジクロロフエニル)ビニルジメチ
ルホスフエート、0、0―ジメチル―0―(3、
5、6―トリクロロ―2―ピリジル)ホスホロチ
オエート、0、0―ジエチル―0―(5―フエニ
ル―3―イソキサゾリル)ホスホロチオエートお
よび0、0―ジエチル―0―(3―オキソ―2―
フエニル―2H―ピリダジン―6―イル)ホスホ
ロチオエートからなる群から選ばれた少くとも1
種以上の化合物を有効成分として含有することを
特徴とする殺虫組成物。
1 3'-phenoxy-α-cyanobenzyl-1-
(4-ethoxyphenyl)-2,2-dichlorocyclopropanecarboxylate and 2-chloro-
1-(2,4-dichlorophenyl)vinyl dimethyl phosphate, 0,0-dimethyl-0-(3,
5,6-trichloro-2-pyridyl) phosphorothioate, 0,0-diethyl-0-(5-phenyl-3-isoxazolyl) phosphorothioate and 0,0-diethyl-0-(3-oxo-2-
at least one selected from the group consisting of phenyl-2H-pyridazin-6-yl) phosphorothioate;
An insecticidal composition characterized by containing more than one species of compound as an active ingredient.
JP56051843A 1981-04-08 1981-04-08 Insecticidal composition Granted JPS57167906A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56051843A JPS57167906A (en) 1981-04-08 1981-04-08 Insecticidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56051843A JPS57167906A (en) 1981-04-08 1981-04-08 Insecticidal composition

Publications (2)

Publication Number Publication Date
JPS57167906A JPS57167906A (en) 1982-10-16
JPS6340405B2 true JPS6340405B2 (en) 1988-08-11

Family

ID=12898128

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56051843A Granted JPS57167906A (en) 1981-04-08 1981-04-08 Insecticidal composition

Country Status (1)

Country Link
JP (1) JPS57167906A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0521014U (en) * 1991-08-30 1993-03-19 東陶機器株式会社 Suspended ceiling structure and suspenders such as suspended ceilings

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0786365B2 (en) * 1987-12-18 1995-09-20 株式会社ミヤナガ Manufacturing method of sleeve
US4919579A (en) * 1987-08-24 1990-04-24 Kabushiki Kaisha Miyanaga Anchor construction and method of manufacture

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5283354A (en) * 1975-11-26 1977-07-12 Commw Scient Ind Res Org Insecticide esters
JPS5362830A (en) * 1976-11-12 1978-06-05 Sumitomo Chem Co Ltd Insecticides comisn for sanitary noxious insects
JPS5583704A (en) * 1978-12-20 1980-06-24 Kuraray Co Ltd Insecticide
JPS5598150A (en) * 1979-01-19 1980-07-25 Sumitomo Chem Co Ltd Carboxylic ester, its preparation and insecticide and acaricide containing the same as an effective component

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5283354A (en) * 1975-11-26 1977-07-12 Commw Scient Ind Res Org Insecticide esters
JPS5362830A (en) * 1976-11-12 1978-06-05 Sumitomo Chem Co Ltd Insecticides comisn for sanitary noxious insects
JPS5583704A (en) * 1978-12-20 1980-06-24 Kuraray Co Ltd Insecticide
JPS5598150A (en) * 1979-01-19 1980-07-25 Sumitomo Chem Co Ltd Carboxylic ester, its preparation and insecticide and acaricide containing the same as an effective component

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0521014U (en) * 1991-08-30 1993-03-19 東陶機器株式会社 Suspended ceiling structure and suspenders such as suspended ceilings

Also Published As

Publication number Publication date
JPS57167906A (en) 1982-10-16

Similar Documents

Publication Publication Date Title
KR101451978B1 (en) Pesticidal Composition for Tree Parastic Pests
JP2002521406A (en) Synergistic residual pest control compounds containing plant essential oils
CN101209047A (en) Synergistic compositions
BG64177B1 (en) New 5-amino-3-cyano-4-ethylsulphanyl-1-phenyl pyrazols and method for their preparation and application as pesticides
SK324392A3 (en) Pesticidal agent and method of suppression of arthropoda
CN104904741B (en) A kind of Pesticidal combination and the method for controlling harmful organism
CN103704255A (en) Sterilization and insecticide composition containing pyraclostrobin
TWI311466B (en)
CN107691446A (en) A kind of Pesticidal combination
JPS6340405B2 (en)
CN105794788B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
CN104904719B (en) A kind of Pesticidal combination and its method for controlling harmful organism
WO2015135420A1 (en) Pesticidal composition and method for controlling pests
CN105794814B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
CN105794811B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
CN105794798B (en) A kind of Pesticidal combination
CN105794828B (en) A kind of Pesticidal combination and its method for controlling pest
CN105707111B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
CN103704258B (en) A kind of Fungicidal insecticidal composition containing abietic acid ketone
JPS6016922B2 (en) insecticidal composition
CN105707115B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
JP3624976B2 (en) Insecticide, acaricide composition
CN105638687B (en) A kind of Pesticidal combination and its method for controlling agricultural pests
JP2832538B2 (en) Acaricidal composition
CN105707078B (en) A kind of Pesticidal combination and its method for controlling agricultural pests