JPS5828849B2 - Resistant leafhopper control agent - Google Patents

Resistant leafhopper control agent

Info

Publication number
JPS5828849B2
JPS5828849B2 JP14544679A JP14544679A JPS5828849B2 JP S5828849 B2 JPS5828849 B2 JP S5828849B2 JP 14544679 A JP14544679 A JP 14544679A JP 14544679 A JP14544679 A JP 14544679A JP S5828849 B2 JPS5828849 B2 JP S5828849B2
Authority
JP
Japan
Prior art keywords
resistant
leafhoppers
control agent
rice
parts
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
JP14544679A
Other languages
Japanese (ja)
Other versions
JPS5671016A (en
Inventor
知 森山
次男 内山
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.)
Hokko Chemical Industry Co Ltd
Original Assignee
Hokko Chemical Industry 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 Hokko Chemical Industry Co Ltd filed Critical Hokko Chemical Industry Co Ltd
Priority to JP14544679A priority Critical patent/JPS5828849B2/en
Publication of JPS5671016A publication Critical patent/JPS5671016A/en
Publication of JPS5828849B2 publication Critical patent/JPS5828849B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、下記の化学構造式で表わされるO−エチル−
〇−O−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」といつ)と1−ナフチルN−
メチルカーバメート(以下「NAC」という)との混合
物を有効成分として含有することを特徴とするカーバメ
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。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides O-ethyl-
〇-O-di(2,4-dichlorophenyl)phosphate (hereinafter referred to as "phosdaifen") and 1-naphthyl N-
The present invention relates to a leafhopper control agent that is resistant to carbamate insecticides and is characterized by containing a mixture with methyl carbamate (hereinafter referred to as "NAC") as an active ingredient.

ツマグロヨコバイは稲に寄生して直接吸収加害するのみ
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 directly absorbs them, but also transmits viral diseases such as rice wilt.

このような本害虫に対し各種のN−メチルカーバメート
系殺虫剤が卓抜した防除効果を示すことから頻繁に利用
されている。
Various N-methyl carbamate insecticides are frequently used because they exhibit outstanding control effects against these pests.

しかしながら、近年西南日本−帯をはじめ各地ではN−
メチルカーバメート系殺虫剤の連用により、固剤に対す
る抵抗性ツマグロヨコバイが出現し、防除に苦慮してい
る現状にある。
However, in recent years, N-
Due to the continuous use of methyl carbamate insecticides, leafhoppers that are resistant to solid agents have appeared, making it difficult to control them.

本発明者ら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NACとの混合物が抵抗性
ツマグロヨコバ−flint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, it was discovered that a mixture of phosdaifen and NAC exhibited a higher control effect on resistant leafminer flint than expected with each agent alone.

本発明の混合剤の成分ホスダイフェンは、特公昭46−
20514号公報に記載された農園芸用殺菌剤であって
、特に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, a component of the mixture of the present invention, is
This is an agricultural and horticultural fungicide described in Japanese Patent Publication No. 20514, which shows particularly excellent control effects against rice blast, but does not have any insecticidal activity at normal concentrations.

一方、NACは、「農薬ハンドブック1976年版」(
日本植物防疫協会発行)の第69〜72頁などにおいて
既知の水稲用殺虫剤であって、感受性のツマグロヨコバ
イには卓効を有スル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, NAC publishes the "Pesticide Handbook 1976 Edition" (
A known insecticide for paddy rice is described in pages 69 to 72 of Japanese Plant Protection Association (Published by the Japanese Plant Protection Association), and although it is highly effective against susceptible leafhoppers, it does not have a sufficient control effect on resistant leafhoppers.

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
イロウンカおよびカメムシ類等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 according to the present invention exhibits a high effect against resistant leafhoppers, becoming an effective agent against the same insect pests, and at the same time, it is effective against pests such as brown-bottomed planthoppers, brown planthoppers, stink bugs, and rice blast disease. It has the advantage of being effective against a wide range of applications.

本発明に係る防除剤は広く使用されている農業用薬剤と
同様に固体、液体等の担体に各種Q)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。
Similar to widely used agricultural chemicals, the pesticidal agent according to the present invention is prepared by adding various Q) auxiliary agents such as surfactants, dispersants, and wetting agents to a solid or liquid carrier to form a powder or hydrate. agents, emulsions,
It can be formulated into granules and used.

本発明の実施例を若干示すが補助剤の種類、添加量およ
び有効成分の混合比率は実施例のみに限定することはな
い。
Although some examples of the present invention are shown below, the types and amounts of adjuvants added and the mixing ratios 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、NAC25部、キシレン35部
およびツルポール(東邦化学工業株製乳化剤)15部を
混合して乳剤とする。
Example 1 (Emulsion) 25 parts of phosdaifen, 25 parts of NAC, 35 parts of xylene, and 15 parts of Tulpol (emulsifier manufactured by Toho Chemical Industries, Ltd.) are mixed to prepare an emulsion.

実施例 2 (粉剤) ホスダイフェン2部、NAC2部、ホワイトカーボン1
部、タルク20部およびクレー75部をヒ均一に混合粉
砕して粉剤とする。
Example 2 (Powder) 2 parts of phosdaifen, 2 parts of NAC, 1 part of white carbon
1 part, 20 parts of talc, and 75 parts of clay were uniformly mixed and pulverized to obtain a powder.

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1001の割合で
ターンテーブル上でスプレーカンにて散布した。
Test Example 1 Resistant leafhopper control effect test A diluted solution of a predetermined concentration of an emulsion prepared according to Example 1 was sprayed on potted paddy rice at the 4th to 5th leaf stage at a rate of 1001 per 10 ares using a spray can on a turntable. .

風乾した後、稲茎葉部を切り取り直径2Cr1′L、長
さ20crIlの大きさの試験管に入れツマグロヨコバ
110頭を故点し24時間後に抑転重数を調べた。
After air-drying, the rice stem leaves were cut and placed in a test tube with a diameter of 2 Cr1'L and a length of 20 Cr Il, and 110 black leafhoppers were killed. 24 hours later, the number of inhibitions was determined.

試験は1濃度3区制で行ない平均抑転虫率(%)を求め
た。
The test was conducted using a three-area system with one concentration, and the average insect inhibition rate (%) was determined.

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カーバメート系殺虫剤に対し高い抵
抗性を示すものである。
The leafhoppers tested were collected from Amakusa, Kumamoto Prefecture and reared for generations, and are highly resistant to carbamate insecticides.

その結果は第1表のとおりである。The results are shown in Table 1.

なお、 期待値ばブリス(B 1iss )の式により求めた。In addition, The expected value was determined using the Bliss equation.

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LC6゜(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
LC6° (5
0% lethal drug concentration) Find the expected value and compare it with the actual value.
The synergistic effect of insecticidal effect by mixing the active ingredients was calculated.

この場合、共力塵が1は相加的効果を示し、1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 less than 1 indicates an antagonistic effect, and a value greater than 2 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.

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°C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。
Changes in the susceptibility of the black leafhopper population due to continuous selection of drugs (from Okayama Prefecture) The black leafhoppers used in the test were collected from rice fields in Kojima District, Okayama Prefecture, and then kept at a constant temperature of 25°C under conditions of 16 hours of light and 8 hours of darkness. This is a product that has been bred for generations using sprouted rice.
These animals were then subjected to selection and rearing, and drug tests were conducted from time to time.

試1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23C1rlX 30C1rLX 2cmの
プ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。
Test 1 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 was sown in a plastic box with a size of 23C1rlX 30C1rLX 2cm, and the sprouted rice seedlings were grown. Sprayed.

この芽出し稲をツマグロヨコバイ飼育ケージに入れ、累
代飼育中のツマグロヨコバイ成虫約1.000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。
The sprouted rice was placed in a cage for raising leafhoppers, and about 1,000 adult leafhoppers were released. After 24 hours, surviving insects were collected with a fluke tube and released into newly prepared sprouted rice plants that were not treated with chemicals. , the next generation population was obtained.

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時間後の生死点数を調査し
、LD5o値(μm/?)を求めた。
For the drug assay, the number of live and dead spots after 24 hours was investigated using a topical application method to adult female leafhoppers 3 to 4 days after emergence, and the LD5o value (μm/?) was determined.

その結果は第3表とおりである。The results are shown in Table 3.

(註1) (註2) 淘汰前の岡山県産のツマグロヨコバイに対するNACの
LD、o値は30.2μP/Pであった。
(Note 1) (Note 2) Before culling, the LD and o values of NAC for leafhoppers from Okayama Prefecture were 30.2 μP/P.

無淘汰系のLD5o値の欄は、薬剤淘汰しないで累代飼
育中のツマグロヨコバイの親成虫、10世代後および2
0世代後のLD、o値(順に淘汰前、10回後、20回
後の欄)を示す。
The LD5o value column for the unselected system shows the parent adults of leafhoppers reared for generations without chemical selection, 10th generation later, and 2nd generation.
The LD and o values after 0 generations (columns before culling, after 10 times, and after 20 times in order) are shown.

Claims (1)

【特許請求の範囲】[Claims] 10−エチル 0−0−ジ(2・4−ジクロルフェニル
)ホスフェートと1−ナフチル N−メチルカーバメー
トとの混合物を有効成分として含有することを特徴とす
る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。
A leafhopper resistant to a carbamate insecticide characterized by containing a mixture of 10-ethyl 0-0-di(2,4-dichlorophenyl) phosphate and 1-naphthyl N-methyl carbamate as an active ingredient. Pesticide.
JP14544679A 1979-11-12 1979-11-12 Resistant leafhopper control agent Expired JPS5828849B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14544679A JPS5828849B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14544679A JPS5828849B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Publications (2)

Publication Number Publication Date
JPS5671016A JPS5671016A (en) 1981-06-13
JPS5828849B2 true JPS5828849B2 (en) 1983-06-18

Family

ID=15385406

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14544679A Expired JPS5828849B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Country Status (1)

Country Link
JP (1) JPS5828849B2 (en)

Also Published As

Publication number Publication date
JPS5671016A (en) 1981-06-13

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