JPS5829921B2 - Resistant leafhopper control agent - Google Patents
Resistant leafhopper control agentInfo
- Publication number
- JPS5829921B2 JPS5829921B2 JP14652479A JP14652479A JPS5829921B2 JP S5829921 B2 JPS5829921 B2 JP S5829921B2 JP 14652479 A JP14652479 A JP 14652479A JP 14652479 A JP14652479 A JP 14652479A JP S5829921 B2 JPS5829921 B2 JP S5829921B2
- Authority
- JP
- Japan
- Prior art keywords
- resistant
- control agent
- rice
- leafhopper
- leafhoppers
- 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
Links
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
【発明の詳細な説明】
本発明は、下記化学構造式で示される〇−エチルー〇・
0−ジ(2・4−ジクロルフェニル)ホスフェート(以
下「ホスダイフェン」という)とジエチル2−fソプロ
ピル−4−メチル−6−ピリミジニルホスホロチオネー
ト(以下「ダイアジノン」という)とを有効成分として
含有することを特徴とする有機燐系殺虫剤およびカーバ
メート系殺虫剤に抵抗性を示すツマグロヨコバイ防除剤
に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to 〇-ethyl〇-
0-di(2,4-dichlorophenyl) phosphate (hereinafter referred to as "phosdaifen") and diethyl 2-f-sopropyl-4-methyl-6-pyrimidinyl phosphorothionate (hereinafter referred to as "diazinon") as active ingredients. The present invention relates to a leafhopper control agent that is resistant to organophosphorus insecticides and carbamate insecticides.
ツマグロヨコバイは稲に寄生して直接吸汗加害するのみ
ならず稲萎縮病等のウィルス病を媒介する稲作の重要害
虫の1種である。The leafhopper is an important pest in rice cultivation that not only parasitizes rice plants and causes direct damage by absorbing sweat, but also transmits viral diseases such as rice wilt.
有機燐系殺虫剤はツマグロヨコバイ、ウンカ類およびニ
カメイチュウ等の稲作害虫防除剤として利用されてきた
。Organophosphorus insecticides have been used as control agents for rice crop pests such as leafhoppers, planthoppers, and stag beetles.
しかし、1960年代に有機燐系殺虫剤に対して抵抗性
を有するツマグロヨコバイが出現して以来ツマグロヨコ
バイ防除剤としてはN−メチルカーバメート系殺虫剤が
頻繁に用いられるようになった。However, since the emergence of the leafhopper resistant to organophosphorus insecticides in the 1960s, N-methyl carbamate insecticides have been frequently used as leafhopper control agents.
ところが、近年西日本−帯をはじめ各地では有機燐系殺
虫剤のみならずNメチルカーバメート系殺虫剤に対して
も抵抗性の発達した、いわゆる複合抵抗性ツマグロヨコ
バイが出現し有効な防除剤がなく苦慮している現状にあ
る。However, in recent years, a so-called compound-resistant leafhopper, which has developed resistance not only to organophosphorus insecticides but also to N-methyl carbamate insecticides, has appeared in various parts of Japan, including western Japan, and it is difficult to find an effective control agent. The current situation is that
本発明者等はこのような現状にかんがみ広汎に研究を重
ねた。The present inventors have conducted extensive research in view of the current situation.
その結果、ホスダイフェンとダイアジノンとの混合剤が
抵抗性ツマグロヨコバイニ対し各単剤では予想もつかな
い程高い防除効果を示すことを発見した。As a result, they discovered that a mixture of phosdaifen and diazinon had a greater control effect on resistant leafhopper than expected with each agent alone.
本発明に係る防除剤の成分の1つであるホスダイフェン
は、特公昭46−20514号公報において記載された
農園芸用殺菌剤であって、イネいもち病に対し優れた防
除効果を示すが常用濃度では恰んど殺虫活性を持たない
。Phosdaifen, which is one of the components of the pest control agent according to the present invention, is an agricultural and horticultural fungicide described in Japanese Patent Publication No. 46-20514, and shows an excellent control effect against rice blast, but it is However, it has no insecticidal activity.
一方、ダイアジノンは、特公昭30−8299号公報な
らびに農薬ハンドブック1976年版第13〜20頁(
日本植物防疫協会発行)などで既知の農園芸用殺虫剤で
あって、水稲用殺虫剤として使用した場合には、感受性
ツマグロヨコバイには有効であるが抵抗性ツマグロヨコ
バイに対し充分な防除効果が得られない。On the other hand, diazinon is reported in Japanese Patent Publication No. 30-8299 and Pesticide Handbook, 1976 edition, pages 13-20 (
It is a known agricultural and horticultural insecticide (published by the Japan Plant Protection Association), and when used as an insecticide for paddy rice, it is effective against susceptible leafhoppers, but does not have a sufficient control effect against resistant leafhoppers. do not have.
本発明に係る防除剤はこれらの2種薬剤を混合すること
により抵抗性ツマグロヨコバイに対し高い殺虫効果を発
揮し同害虫の有効剤になると同時にヒメトビウンカ、ト
ビイロウンカ、ニカメイチュウおよびカメムシ類などの
害虫およびイネいもち病に対しても有効であり適用範囲
が広い利点を有する。By mixing these two types of chemicals, the pesticidal agent of the present invention exhibits a high insecticidal effect against resistant leafhoppers, and is an effective agent against the same insect pests. It has the advantage of being effective against diseases and having a wide range of applications.
本発明に係る防除剤は一般の農業用薬剤と同様に固体、
液体等の担体に各種の界面活性剤、分散剤、湿展剤等の
補助剤を添加して粉剤、水和剤、乳剤、粒剤等に製剤化
して使用できる。The pesticidal agent according to the present invention is solid, similar to general agricultural chemicals.
It can be formulated into powders, wettable powders, emulsions, granules, etc. by adding various auxiliary agents such as surfactants, dispersants, and wetting agents to a carrier such as a liquid.
次に本発※※明の実施例を若干示すが補助剤の種類およ
び有効成分の混合比率は実施例のみに限定されることは
ない。Next, some examples of the present invention will be shown, but the types of adjuvants and the mixing ratio of active ingredients are not limited to the examples.
なお、実施例中部は全て重量部を示す。Note that all figures in the middle part of the examples indicate parts by weight.
実施例 1
(乳剤)
ホスダイフェン25部、ダイアジノン25部、キシレン
35部およびツルポール(東邦化学工業株式会社製乳化
剤)15部を混合して乳剤とする。Example 1 (Emulsion) 25 parts of phosdaifen, 25 parts of diazinon, 35 parts of xylene, and 15 parts of Tulpol (emulsifier manufactured by Toho Chemical Industries, Ltd.) are mixed to prepare an emulsion.
ノ 実施例 2
(粉剤)
ホスダイフェン2部、ダイアシッフ2部、ホワイトカー
ボン1部、タルク20部およびクレー75部を均一に混
合粉砕して粉剤とする。Example 2 (Powder) 2 parts of Phosdaifen, 2 parts of Diaschiff, 1 part of white carbon, 20 parts of talc and 75 parts of clay are uniformly mixed and ground to obtain a powder.
5 試験例 1
抵抗性ツマグロヨコバイ防除効果試験
4〜5葉期の鉢植水稲に実施例1に準じて調製した乳剤
の所定濃度希釈液を10アールあたり1007の割合で
ターンテーブル上でスプレーガン ンにて散布した。5 Test Example 1 Resistant leafhopper control effect test A diluted solution of a predetermined concentration of the emulsion prepared according to Example 1 was applied to potted paddy rice at the 4th to 5th leaf stage at a rate of 1007 per 10 ares using a spray gun on a turntable. Spread.
風乾した後、稲茎葉部を切り取り直径2cm、長さ20
CrILの大きさの試験管に入れツマグロヨコバイ10
頭を放生し24時間後に仰転虫数を調べた。After air-drying, cut the rice stem leaves to a diameter of 2 cm and a length of 20 cm.
Put 10 black leafhoppers into a test tube the size of CrIL.
The number of supine insects was determined 24 hours after the heads were released.
なお供試したツマグロヨコバイは熊本県天草より採集し
累代飼育したもので有機燐系殺虫剤およびN−メチルカ
ーバメート系殺虫剤に対し複合抵抗性を示す。The leafhoppers used in the experiment were collected from Amakusa, Kumamoto Prefecture, and reared for generations, and exhibited combined resistance to organophosphorus insecticides and N-methylcarbamate insecticides.
本試験は1区10頭の3区制で行ない平均仰転虫率(%
)を求めた。This test was conducted in three sections with 10 animals per section, and the average supine insect rate (%
) was sought.
その結果は第1表のとおりである。The results are shown in Table 1.
なお、期待値はブリス(B115s )の式により求め
た。Note that the expected value was determined using the Bliss (B115s) formula.
第1表のデータに基づいて、カーペンタ−(Carpe
nter et al )の式によりLC5o(5
0%致死薬剤濃度)期待値を求め、実測値との対比から
、有効成分を混合することによる殺虫効果の共力塵を算
出した。Based on the data in Table 1, Carpenter
LC5o(5
The expected value (0% lethal drug concentration) was determined, and the synergistic effect of the insecticidal effect by mixing the active ingredients was calculated from the comparison with the actual value.
この場合、共力塵が1は相加的効果を示し、■より小さ
い場合は拮抗的効果を示し、■より大きい場合は相乗的
効果を示す。In this case, a synergistic value of 1 indicates an additive effect, a value smaller than ■ indicates an antagonistic effect, and a value greater than ■ indicates a synergistic effect.
そして、共力塵が2以上の場合は相乗的効果が顕著であ
ることを示す。When the number of synergistic particles is 2 or more, it indicates that the synergistic effect is significant.
その結果は、第2表のとおりである。The results are shown in Table 2.
試験例 2
薬剤の連続淘汰によるツマグロヨコバイ個体群の感受性
の変化(岡山県産)
供試したツマグロヨコバイは、岡山県児島郡の水田より
採集した後、25℃の恒温下で16時間照明、8時間暗
黒条件下にて芽出し稲を用いて累代飼育したもので、こ
れをその後の淘汰ならびに飼育に供し、随時薬剤検定を
行った。Test Example 2 Changes in the susceptibility of the black leafhopper population due to continuous selection of drugs (produced in Okayama Prefecture) The black leafhopper used in the test was collected from a rice field in Kojima District, Okayama Prefecture, and then kept at a constant temperature of 25°C under light for 16 hours and darkness for 8 hours. The rice was bred for generations using sprouted rice under the following conditions, and was subsequently subjected to culling and breeding, and drug tests were conducted from time to time.
試験方法としては、まず実施例1に準じて調製した供試
薬剤の淘汰率50%前後の薬剤濃度希釈液10m1を、
大きさが23CTL×30cfrL×2CTLのグラス
チック箱に播種し育苗した芽出し稲に噴霧処理した。As a test method, first, 10 ml of a drug concentration diluted solution with a selection rate of around 50% of the test drug prepared according to Example 1,
The seeds were sown in a plastic box with a size of 23 CTL x 30 cfrL x 2 CTL, and the sprouted rice seedlings were then sprayed.
この芽出し稲をツマグロヨコバイM育ケージに入れ、累
代飼育中のツマグロヨコバイ成虫約1000頭を放ち、
24時間後に生存虫を吸虫管にて採取し、別途用意した
薬剤無処理の芽出し稲に放飼し、次世代の個体群を得た
。This sprouted rice was placed in a cage for raising black leafhoppers, and approximately 1,000 adult black leafhoppers, which were being reared for generations, were released.
After 24 hours, the surviving insects were collected with a fluke tube and released into newly prepared sprouted rice plants that were not treated with chemicals to obtain the next generation population.
同様な方法で1世代1回の割合で淘汰をくり返した。Selection was repeated in the same manner, once per generation.
薬剤検定は、羽化3〜4日後のツマグロヨコバイ雌成虫
に対し局所施用法による24時間後の生死虫数を調査し
、LD5o値(μm/1)を求めた。In the drug test, the number of live and dead insects was investigated after 24 hours by topical application to adult female leafhoppers 3 to 4 days after emergence, and the LD5o value (μm/1) was determined.
その結果は第3表のとおりである。The results are shown in Table 3.
Claims (1)
ルー4−メチル−6−ピリミジニルホスホロチオネート
とを有効成分として含有することを特徴とする有機燐系
殺虫剤およびカーバメート系殺虫剤に抵抗性を示すツマ
グロヨコバイ防除剤。[Claims] It is characterized by containing 10-ethyl 0.0 di(2-dichloro* *phenyl) phosphate and diethyl 2-isofuropyru-4-methyl-6-pyrimidinyl phosphorothioate as active ingredients. A leafhopper control agent that is resistant to organophosphorus insecticides and carbamate insecticides.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14652479A JPS5829921B2 (en) | 1979-11-14 | 1979-11-14 | Resistant leafhopper control agent |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14652479A JPS5829921B2 (en) | 1979-11-14 | 1979-11-14 | Resistant leafhopper control agent |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5671019A JPS5671019A (en) | 1981-06-13 |
| JPS5829921B2 true JPS5829921B2 (en) | 1983-06-25 |
Family
ID=15409591
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14652479A Expired JPS5829921B2 (en) | 1979-11-14 | 1979-11-14 | Resistant leafhopper control agent |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5829921B2 (en) |
-
1979
- 1979-11-14 JP JP14652479A patent/JPS5829921B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5671019A (en) | 1981-06-13 |
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