JPH03215402A - Disturbing agent of mating behavior of plusia nigrisigna - Google Patents

Disturbing agent of mating behavior of plusia nigrisigna

Info

Publication number
JPH03215402A
JPH03215402A JP988390A JP988390A JPH03215402A JP H03215402 A JPH03215402 A JP H03215402A JP 988390 A JP988390 A JP 988390A JP 988390 A JP988390 A JP 988390A JP H03215402 A JPH03215402 A JP H03215402A
Authority
JP
Japan
Prior art keywords
preparation
mating behavior
dodecenol
active ingredients
acetate
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.)
Granted
Application number
JP988390A
Other languages
Japanese (ja)
Other versions
JP3013933B2 (en
Inventor
Akira Yamamoto
昭 山本
Toshiaki Ihara
俊明 井原
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.)
Shin-Etsu Chemical Co Ltd
Original Assignee
Shin-Etsu Chemical 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 Shin-Etsu Chemical Co Ltd filed Critical Shin-Etsu Chemical Co Ltd
Priority to JP988390A priority Critical patent/JP3013933B2/en
Publication of JPH03215402A publication Critical patent/JPH03215402A/en
Application granted granted Critical
Publication of JP3013933B2 publication Critical patent/JP3013933B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

PURPOSE:To obtain a preparation for disturbing mating behavior of male imagoes of Plusia nigrisigna to prevent multiplication thereof, comprising Z-7- dodecenyl acetate and Z-7-dodecenol as active ingredients. CONSTITUTION:The title preparation comprising Z-7-dodecenyl acetate and Z-7-dodecenol in the ratio of (97:3)-(3:97) [preferably (80:20)-(20:80)]. The preparation may be mixed with sex pheromone constituent component of other insect, sex attractant, antioxidant, ultraviolet light absorber, etc. In order to maintain release of active ingredients for many hours, preferably the preparation is packed into capillary, bag made of laminated film or container such as capsule comprising a plastic such as polyethylene, polypropylene, ethylene-vinyl acetate copolymer or polyvinyl chloride having release amount-controlling function and used.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、キャベツ、白菜、ごぼう、レタス、大豆,人
参、せり、薩摩芋等の野菜に被害を与えるタマナギンウ
ワバの雄成虫の配偶行動を撹乱して個体の増殖を妨げそ
の防除を行う、性フエ口モンおよび誘引物質を有効成分
とするタマナギンウワバの配偶行動撹乱剤に関するもの
である。
[Detailed Description of the Invention] (Industrial Application Field) The present invention disrupts the mating behavior of male adult beetles of the Japanese cabbage moth, which damages vegetables such as cabbage, Chinese cabbage, burdock, lettuce, soybeans, carrots, parsley, and satsuma potatoes. The present invention relates to a mating behavior disrupting agent for the turmeric, which contains as active ingredients a sex phlegm and an attractant, and prevents and controls the proliferation of individuals.

(従来の技術) タマナギンウワバはコナガやモンシロチョウなどと共に
、我が国における野菜の主要害虫としてよく知られてい
る。この防除には、これまで有機りん系、カーバメイト
系およびステロイド系等の多くの殺虫剤が使われてきた
。しかし、これらの殺虫剤は、散布者に薬害または中毒
症状をもたらす危険性が高い、散布を継続すると殺虫剤
に対する抵抗性の高い虫が出現して薬効が低下する、作
物への残留性や環境汚染の危険性があるなどの問題を抱
えているため、毒性のない農薬や農薬を使わない栽培方
法の開発が望まれてきた。
(Prior Art) Along with diamondback moth and cabbage moth, it is well known as a major pest of vegetables in Japan. Many insecticides such as organophosphorus, carbamate, and steroid insecticides have been used for this control. However, these pesticides have a high risk of causing chemical damage or poisoning symptoms to the sprayer, and if spraying continues, insects with high resistance to the pesticide will appear, reducing the efficacy of the pesticide. Due to problems such as the risk of contamination, there has been a desire to develop non-toxic pesticides and cultivation methods that do not use pesticides.

その一つとして近年人工的に合成した昆虫の性フエ口モ
ンを用いるクリーンな昆虫防除方法が開発され、既に茶
のハマキムシ類、果樹のシンクイムシやコスカシバ、野
菜を食害するコナガにおいて実用化されている。
One example of this is the recent development of a clean insect control method using artificially synthesized insect fetomitomes, which has already been put to practical use against tea leaf beetles, fruit trees' sink beetles and kosuka moths, and the diamondback moth, which damages vegetables. .

この性フエ口モンによる防除は標的害虫にのみ効果を及
ぼし、人間や他の生物に対して全く毒性がないだけでな
く、作物における残留性や環境汚染の危険性もなく、従
来の農薬の抱えていた諸問題を解決できる方法である。
This insect pest control is effective only on target pests and is not only completely non-toxic to humans and other living organisms, but also has no residue in crops or environmental contamination risk, which is a problem that traditional pesticides have. This is a method that can solve the various problems that have arisen.

(発明が解決しようとする課題) 本発明の目的は、野菜の主要害虫として知られているタ
マナギンウワバを防除するのに有効な性フェロモンおよ
び誘引物質を有効成分とする配偶行動撹乱剤を提供しよ
うとするものである。
(Problems to be Solved by the Invention) An object of the present invention is to provide a mating behavior disrupting agent containing a sex pheromone and an attractant as active ingredients, which is effective for controlling the common pest known as a major pest of vegetables. It is something to do.

(課題を解決するための手段) 本発明は、タマナギンウワバの配偶行動撹乱剤として、
97:3〜3:97の割合のZ−7−ドデセニルアセテ
ートとZ−7−ドデセノールとを有効成分として含有す
るものとしたことを要旨とするものである。
(Means for Solving the Problems) The present invention provides a method for disrupting mating behavior of A.
The gist thereof is to contain Z-7-dodecenyl acetate and Z-7-dodecenol in a ratio of 97:3 to 3:97 as active ingredients.

これを説明すると、本発明によるタマナギンウワバの配
偶行動撹乱剤は、Z−7−ドデセニルアセテートとZ−
7−ドデセノールとを有効成分として含有するものであ
るが、この両成分の割合は97:3〜3:97.好まし
くは80 : 20〜20 : 80の範囲内であるこ
とが必要で、この範囲外では効果が劣る。
To explain this, the mating behavior disrupting agent of the present invention contains Z-7-dodecenyl acetate and Z-
It contains 7-dodecenol as an active ingredient, and the ratio of both ingredients is 97:3 to 3:97. Preferably, the ratio should be within the range of 80:20 to 20:80, and the effect will be poor outside this range.

上記配偶行動撹乱剤には、上記成分のほかに、さらにヨ
トウガ、コナガ、シロイチモンジ扇トウ、ハスモンヨト
ウ、タバコガ、アワヨトウ、イラクサギンウワバなど野
菜を食害する他の昆虫の性フェロモン構成成分や性誘引
物質を添加して、タマナギンウワバと同時に、これらの
昆虫の配偶行動を撹乱してもよく、この目的のための性
フエ口モン構成成分および性誘引物質としては,例えば
Z,E−9.12−テトラデ力ジエニルアセテート、Z
,E−9,1l−テトラデ力ジエニルアセテート、Z−
9−テトラデセノール、Z−11−ヘキサデセニルアセ
テート、Z−11−へキサデセノール、Z−7−テトラ
デセニルアセテート、Z−11−へキサデセナール、Z
−9−へキサデセナール、11−ドデセニルアセテート
、n−ドデセニルアセテート、Z−5−ドデセニルアセ
テート、Z−9−テトラデセニルアセテートなどが挙げ
られる。
In addition to the above-mentioned ingredients, the above-mentioned mating behavior disruptors include sex pheromone components and sex attractants of other insects that damage vegetables, such as armyworm moth, diamondback moth, Japanese armyworm, Japanese armyworm, tobacco moth, fall armyworm, and stinging nettle. may be added to disrupt the mating behavior of these insects at the same time as tamanaginuwaba, and examples of sexual fematome constituents and sex attractants for this purpose include, for example, Z,E-9.12-tetrade. force dienylacetate, Z
, E-9,1l-tetradedienylacetate, Z-
9-tetradecenol, Z-11-hexadecenyl acetate, Z-11-hexadecenol, Z-7-tetradecenyl acetate, Z-11-hexadecenal, Z
-9-hexadecenal, 11-dodecenyl acetate, n-dodecenyl acetate, Z-5-dodecenyl acetate, Z-9-tetradecenyl acetate, and the like.

また、この配偶行動撹乱剤には、ブチルヒドロキシトル
エン、プチルヒドロキシアニソール、ハイドロキノン、
ビタミンE,N−2−オクチルーN’−フェニルーP−
フ二二レンジアミン等の抗酸化剤や4−ヒドロキシ−4
−オクトキシベンゾフエノン等の紫外線吸収剤を適量加
えてもよい。
In addition, these mating behavior disruptors include butylated hydroxytoluene, butylated hydroxyanisole, hydroquinone,
Vitamin E, N-2-octyl-N'-phenyl-P-
Antioxidants such as fluorinated diamine and 4-hydroxy-4
- An appropriate amount of ultraviolet absorber such as octoxybenzophenone may be added.

本発明による配偶行動撹乱剤は、有効成分として含有す
る上記性フエ口モンおよび誘引物質の放出を長期間にわ
たって持続させるために、これを例えば、特開昭56−
142202号、57−9705号、−50901号、
−72904号、−156403号、5B−18360
1号、59−216802号, 60−215367号
、61−202643号,62−195303号、−2
23101号、−258301号, 63−22530
3号、および64一75402号各公報、実開昭57−
51532号、−51533号、61−43201号.
 62−122801号、および64−45974号各
公報に記載の、ポリエチレン、ポリプロピレン、エチレ
ンー酢酸ビニル共重合体、ポリ塩化ビニル等の放出量制
御機能を有するプラスチックからなる細管、ラミネート
フイルム製の袋、カプセル等の容器に充填して用いられ
る。
The mating behavior disrupting agent according to the present invention has the advantage that, in order to sustain the release of the above-mentioned sex phlegm and attractant contained as active ingredients over a long period of time, it is
No. 142202, No. 57-9705, No. -50901,
-72904, -156403, 5B-18360
No. 1, No. 59-216802, No. 60-215367, No. 61-202643, No. 62-195303, -2
23101, -258301, 63-22530
3 and 64-175402, Utility Model Application Publication No. 1987-
No. 51532, No. -51533, No. 61-43201.
62-122801 and 64-45974, thin tubes, laminate film bags, and capsules made of plastics having a release control function such as polyethylene, polypropylene, ethylene-vinyl acetate copolymer, polyvinyl chloride, etc. It is used by filling it into containers such as

(実施例) 以ド、本発明の具体的態様を実施例および比較例により
説明するが、本発明はこの実施例の記載に限定されるも
のではない。
(Examples) Hereinafter, specific aspects of the present invention will be explained using Examples and Comparative Examples, but the present invention is not limited to the description of these Examples.

実施例 1〜4.および比較例 1〜4.内径0.8m
m、外径1.6m++のポリエチレン製の管を2本、軸
方向に並列し、表面で接合した形態の徐放体(特開昭5
7−156403号公報参照)の一方の管にアルミニウ
ム線を封入して杭やポールに巻き付けやすくすると共に
他方の管に、表に記載の性フェロモン物質にその0.5
重量%の抗酸化剤としてのプチルヒドロキシトルエンを
加えたものを充填し、200 m置きにシールした10
0mの長さの製剤を作成した。但し、実施例2と比較例
2では徐放体の材料としてポリエチレンに代えてエチレ
ンー酢酸ビニル共重合体(酢酸ビニル含量6%)を用い
たものを使用した。
Examples 1-4. and Comparative Examples 1-4. Inner diameter 0.8m
sustained-release body (Japanese Unexamined Patent Application Publication No. 1983-1999
(Refer to Publication No. 7-156403), one tube is filled with aluminum wire to make it easier to wrap around stakes and poles, and the other tube is filled with 0.5 of the sex pheromone substances listed in the table.
10 filled with wt% butylated hydroxytoluene as an antioxidant and sealed every 200 m.
A preparation with a length of 0 m was prepared. However, in Example 2 and Comparative Example 2, an ethylene-vinyl acetate copolymer (vinyl acetate content: 6%) was used instead of polyethylene as the material for the sustained release body.

7月4日に定植の完了したキャベツ畑を、各区画の面積
が30aで正方形に近い形状をしている8試験区に分け
、7月14F−1に慣用防除区(比較例3)と無処理区
(比較例4)とを除く各試験区(実施例1〜4、比較例
1〜2)において、畑の畝の端から端までに約Ion間
隔で支柱を立て、その高さ401の位置に表に示した各
製剤を巻き付けながら畝上を張り渡した。この作業を畝
と直角の方向に8〜10m間隔で行った。また慣行防除
区では殺虫剤を6回散布し、無処理区では何の処理も行
わなかった。
The cabbage field for which planting was completed on July 4th was divided into 8 test plots, each having an area of 30 a and a shape similar to a square. In each test plot (Examples 1 to 4, Comparative Examples 1 to 2) except for the treated plot (Comparative Example 4), poles were erected at intervals of about 1 ion from one end of the field ridge to the other, and the height of the poles was 401 cm. The ridges were stretched while wrapping each of the preparations shown in the table at the positions shown in the table. This work was performed at intervals of 8 to 10 m in the direction perpendicular to the ridges. Insecticides were sprayed six times in the conventional control areas, and no treatment was applied in the non-treated areas.

全試験区の中央部にはタマナギンウヮバの処女雌を誘引
源とする粘着トラップを設置し、それぞれの試験区にお
けるタマナギンウワバの雄成虫の誘殺数を9月13日ま
で連続的に調査することにより、配偶行動がどの位撹乱
されたかの目安とした。
Adhesive traps were set up in the center of all test plots, using virgin females of the Tamanaginuwaba as an attraction source, and the number of male adult Tamanaginuwaba attracted in each test plot was continuously surveyed until September 13th. This was used as a measure of how much behavior was disturbed.

配偶行動に対する撹乱の度合は、次式より導き出される
交信撹乱率によって示した。
The degree of disturbance to mating behavior was expressed by the mating disturbance rate derived from the following equation.

また、期間中の各フェロモン物質の放出速度は13(1
− 150+ng / 10a・日、製剤の使用量は1
00m/10aであった。
In addition, the release rate of each pheromone substance during the period was 13 (1
- 150+ng/10a・day, the dosage of the preparation is 1
00m/10a.

試験の結果は表に併記した。なお、表中の符号は次を意
味する。
The test results are also listed in the table. Note that the symbols in the table have the following meanings.

Z−7−12−AC: Z−7−ドデセニルアセテート
Z−7−12−OH: Z−7−ドデセノールZ−11
−16−AL : Z−11−へキサデセナールZ−1
1−16−AC : Z−11−ヘキサデセニルアセテ
ート表から判るように、Z−7−ドデセニルアセテート
とZ−7−ドデセノールとが、97:3〜3:97の割
合で有効成分として含有するものをポリエチレンチュー
ブに封入した製剤は、いずれも95%を超える高い交信
撹乱率を示し、極めて強力なタマナギンウワバに対する
配偶行動撹乱作用のあることが確誌された。
Z-7-12-AC: Z-7-dodecenyl acetate Z-7-12-OH: Z-7-dodecenol Z-11
-16-AL: Z-11-hexadecenal Z-1
1-16-AC: Z-11-hexadecenyl acetate As seen from the table, Z-7-dodecenyl acetate and Z-7-dodecenol are effective at a ratio of 97:3 to 3:97. All of the preparations containing the ingredients encapsulated in polyethylene tubes showed a high communication disruption rate of over 95%, and it was confirmed that they had an extremely strong mating behavior-disrupting effect on red-bellied cockroaches.

(発明の効果) 本発明の配偶行動撹乱剤はタマナギンウヮバに対し極め
て強力に作用するので、その防除に有効である。
(Effects of the Invention) The mating behavior disrupting agent of the present invention has an extremely strong effect on T. sinensis and is therefore effective in controlling it.

−7-7

Claims (1)

【特許請求の範囲】[Claims] 1、97:3〜3:97の割合のZ−7−ドデセニルア
セテートとZ−7−ドデセノールとを有効成分として含
有するタマナギンウワバの配偶行動撹乱剤。
1. A mating behavior disrupting agent for A. chinensis, which contains Z-7-dodecenyl acetate and Z-7-dodecenol in a ratio of 1,97:3 to 3:97 as active ingredients.
JP988390A 1990-01-19 1990-01-19 Mating behavior disrupting agent of tamanagin uwaba Expired - Fee Related JP3013933B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP988390A JP3013933B2 (en) 1990-01-19 1990-01-19 Mating behavior disrupting agent of tamanagin uwaba

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP988390A JP3013933B2 (en) 1990-01-19 1990-01-19 Mating behavior disrupting agent of tamanagin uwaba

Publications (2)

Publication Number Publication Date
JPH03215402A true JPH03215402A (en) 1991-09-20
JP3013933B2 JP3013933B2 (en) 2000-02-28

Family

ID=11732552

Family Applications (1)

Application Number Title Priority Date Filing Date
JP988390A Expired - Fee Related JP3013933B2 (en) 1990-01-19 1990-01-19 Mating behavior disrupting agent of tamanagin uwaba

Country Status (1)

Country Link
JP (1) JP3013933B2 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006232851A (en) * 1998-01-30 2006-09-07 Shin Etsu Chem Co Ltd Sustained release pheromone formulation
JP2010018543A (en) * 2008-07-10 2010-01-28 Shin-Etsu Chemical Co Ltd Sexual pheromone substance of platyptilia ignifera, and sex attractant comprising the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2006232851A (en) * 1998-01-30 2006-09-07 Shin Etsu Chem Co Ltd Sustained release pheromone formulation
JP2010018543A (en) * 2008-07-10 2010-01-28 Shin-Etsu Chemical Co Ltd Sexual pheromone substance of platyptilia ignifera, and sex attractant comprising the same

Also Published As

Publication number Publication date
JP3013933B2 (en) 2000-02-28

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