JP3013933B2 - Mating behavior disrupting agent of tamanagin uwaba - Google Patents

Mating behavior disrupting agent of tamanagin uwaba

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Publication number
JP3013933B2
JP3013933B2 JP988390A JP988390A JP3013933B2 JP 3013933 B2 JP3013933 B2 JP 3013933B2 JP 988390 A JP988390 A JP 988390A JP 988390 A JP988390 A JP 988390A JP 3013933 B2 JP3013933 B2 JP 3013933B2
Authority
JP
Japan
Prior art keywords
mating behavior
disrupting agent
acetate
tamanagin
uwaba
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 - Fee Related
Application number
JP988390A
Other languages
Japanese (ja)
Other versions
JPH03215402A (en
Inventor
昭 山本
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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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、性フェロ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 relates to cabbage, Chinese cabbage, burdock, lettuce, soybean,
The present invention relates to an agent that disrupts the mating behavior of Tamanaginiwawa, which contains a sex pheromone and an attractant as an active ingredient, which disrupts the mating behavior of the adult male Tamanaginawawa, which damages vegetables such as carrots, seri, sweet potatoes, and inhibits the growth of individuals. Things.

(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) Tamanaginubawa is well known as a major insect pest of vegetables in Japan, along with Japanese moth and white butterfly. Many pesticides such as organophosphorus, carbamate and steroid have been used for this control. However, these insecticides have a high risk of causing harm or poisoning to the sprayer, and if the spraying is continued, insects with high resistance to the insecticide will appear and their efficacy will decrease,
Because of problems such as persistence in crops and danger of environmental pollution, it has been desired 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ェロ
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。
In recent years, clean insect control methods using artificially synthesized insect sex pheromones have been developed as one of them, and tea leaf bugs, fruit tree sink beetles and cosmosophila,
It has been put to practical use in Konaga, which damages vegetables.

この性フェロ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 sex pheromone control only works on the target pest, not only with no toxicity to humans and other organisms, but also without the risk of persistence or environmental pollution in crops,
This is a method that can solve various problems of conventional pesticides.

(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 sex-matter disrupting agent containing a sex pheromone and an attractant as effective ingredients for controlling Tamanaginuwaba, which is known as a major pest of vegetables. Is what you 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 an active ingredient comprising Z-7-dodecenyl acetate and Z-7-dodecenol in a ratio of 97: 3 to 3:97 as a mating behavior disrupting agent for Tamanaginubawa. The gist is that it is contained as.

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8
0:20〜20:80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。
Explaining this, the mate disturbing agent of Tamanaginubawa according to the present invention is composed of Z-7-dodecenyl acetate and Z-7-dodecenyl acetate.
-7-dodecenol as an active ingredient, and the ratio of these two components is 97: 3 to 3:97, preferably 8: 3.
It is necessary to be within the range of 0:20 to 20:80, and the effect is inferior 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、シロイチモンジョトウ、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
性フェロ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−テトラデカジエニルアセテート、Z,E−9,
11−テトラデカ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
−ヘキサデセノール、Z−7−テトラデセニルアセテー
ト、Z−11−ヘキサデセナール、Z−9−ヘキサデセナ
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。
The spouse behavior disrupting agent, in addition to the above-mentioned components, furthermore, sex pheromone components and sex attractants of other insects that injure vegetables such as armyworm, moth moth, white-spotted armyworm, tossin armyworm, tobacco moth, armyworm, and nettle May be added to simultaneously disrupt the mating behavior of these insects, and the sex pheromone component and sex attractant for this purpose may be, for example, Z, E-9,12-tetradecadiene. Enyl acetate, Z, E-9,
11-tetradecadienyl acetate, 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、ブ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−N′−フェニル−
P−フェニ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ェノン等の紫外線吸収剤を適
量加えてもよい。
Further, the spousal behavior disrupting agents include butylhydroxytoluene, butylhydroxyanisole, hydroquinone, vitamin E, N-2-octyl-N'-phenyl-
An appropriate amount of an antioxidant such as P-phenylenediamine or an ultraviolet absorber such as 4-hydroxy-4-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
する上記性フェロ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、−1564
03号、58−183601号、59−216802号、60−215367号、61
−202643号、62−195303号、−223101号、−258301号、
63−225303号、および64−75402号各公報、実開昭57−5
1532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−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、ラミネートフィルム製の袋、カプセル等の容器に
充填して用いられる。
In order to maintain the release of the sex pheromone and the attractant contained as an active ingredient over a long period of time, the spouse disrupting agent according to the present invention may be prepared by, for example,
142202, 57-9705, -50901, -72904, -1564
03, 58-183601, 59-216802, 60-215367, 61
-202643, 62-195303, -223101, -258301,
Nos. 63-225303 and 64-75402, Jpn.
Nos. 1532, -51533, 61-43201, 62-122801, and 64-45974, each of which discloses a polyethylene, polypropylene, ethylene-vinyl acetate copolymer, and a release control function for polyvinyl chloride and the like. It is used by filling it into containers such as thin tubes made of plastics, bags made of laminated films, capsules and the like.

(実施例) 以下、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 embodiments of the present invention will be described with reference to Examples and Comparative Examples, but the present invention is not limited to the descriptions of the Examples.

実施例 1〜4.および比較例 1〜4. 内径0.8mm、外径1.6mm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
57−156403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
抗酸化剤としてのブチルヒドロキシトルエンを加えたも
のを充填し、200mm置きにシールした100m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−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. Two polyethylene pipes having an inner diameter of 0.8 mm and an outer diameter of 1.6 mm,
A sustained-release body in the form of being parallel in the axial direction and joined at the surface
In one tube, an aluminum wire is sealed so as to be easily wound around a stake or a pole, and in the other tube, 0.5% by weight of butyl as an antioxidant is added to the sex pheromone substance shown in the table. Hydroxytoluene was added and filled to prepare a 100-m-long preparation sealed every 200 mm. However, in Example 2 and Comparative Example 2, a material using an ethylene-vinyl acetate copolymer (vinyl acetate content 6%) instead of polyethylene was used as the sustained release material.

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14日に慣用防除区(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10m間隔で支
柱を立て、その高さ40cm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 that had been completely planted on July 4 was divided into eight test plots, each of which had an area of 30a and a shape close to a square. On July 14, a common control plot (Comparative Example 3) was untreated. Test sections (Examples 1 to 4, Comparative Examples 1 to 4) except for the test section (Comparative Example 4).
In 2), columns were erected at intervals of about 10 m from one end of the ridge to the other end of the field, and the respective preparations shown in the table were wound around the ridge at a position of 40 cm in height. This operation was performed at a distance of 8 to 10 m in a direction perpendicular to the ridge. In the conventional control area, the insecticide was sprayed 6 times, and in the untreated area, no treatment was performed.

全試験区の中央部にはタマナギンウワバの処女雌を誘
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有殺数を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。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。
In the central part of all test plots, an adhesive trap was set up using the virgin female of Tamanaginuwaba as an attraction source, and by continuously investigating the number of male adults of Tamanaginiwawa in each test plot until September 13, It was a measure of how much marital behavior was disrupted. The degree of disturbance to marital behavior was indicated by a communication 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130〜1
50mg/10a・日、製剤の使用量は100m/10aであった。
Also, the release rate of each pheromone substance during the period is 130 to 1
The dosage of the preparation was 50 mg / 10a.day, and the amount used was 100 m / 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 shown in the table. The symbols in the table mean the following.

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−ヘキサデセナール Z−11−16−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認された。
Z-7-12-AC: Z-7-dodecenyl acetate Z-7-12-OH: Z-7-dodecenol Z-11-16-AL: Z-11-hexadecenal Z-11-16-AC : Z-11-hexadecenyl acetate As can be seen from the table, the formulation in which Z-7-dodecenyl acetate and Z-7-dodecenol are contained as active ingredients in a ratio of 97: 3 to 3:97 in a polyethylene tube, Also showed a high communication disruption rate of over 95%, confirming that it had a very strong effect of disrupting mating behavior on Tamanaginuwaba.

(発明の効果) 本発明の配偶行動撹乱剤はタマナギンウワバに対し極
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 agent for disrupting mating behavior of the present invention acts extremely strongly on Tamanaginuwaba and is therefore effective in controlling it.

───────────────────────────────────────────────────── フロントページの続き (72)発明者 井原 俊明 新潟県中頚城郡頚城村大字西福島28番地 の1 信越化学工業株式会社合成技術研 究所内 (56)参考文献 特開 昭59−59602(JP,A) ────────────────────────────────────────────────── ─── Continuing from the front page (72) Inventor Toshiaki Ihara 28-1, Nishifukushima, Oku-ku, Kutsugi-mura, Nakatsukushiro-gun, Niigata Pref. Shin-Etsu Chemical Co., Ltd. , A)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項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. An agent for disrupting mating behavior of Tamanaginubawa, comprising as active ingredients Z-7-dodecenyl acetate and Z-7-dodecenol in a ratio of 97: 3 to 3:97.
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 JPH03215402A (en) 1991-09-20
JP3013933B2 true 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)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4657981B2 (en) * 1998-01-30 2011-03-23 信越化学工業株式会社 Sustained release pheromone formulation
JP5022317B2 (en) * 2008-07-10 2012-09-12 信越化学工業株式会社 Sexual pheromone substance of grape giant bird and sex attractant containing the same

Also Published As

Publication number Publication date
JPH03215402A (en) 1991-09-20

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