JPS5828847B2 - Resistant leafhopper control agent - Google Patents

Resistant leafhopper control agent

Info

Publication number
JPS5828847B2
JPS5828847B2 JP14544479A JP14544479A JPS5828847B2 JP S5828847 B2 JPS5828847 B2 JP S5828847B2 JP 14544479 A JP14544479 A JP 14544479A JP 14544479 A JP14544479 A JP 14544479A JP S5828847 B2 JPS5828847 B2 JP S5828847B2
Authority
JP
Japan
Prior art keywords
control agent
resistant
leafhopper
test
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
Application number
JP14544479A
Other languages
Japanese (ja)
Other versions
JPS5671014A (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 JP14544479A priority Critical patent/JPS5828847B2/en
Publication of JPS5671014A publication Critical patent/JPS5671014A/en
Publication of JPS5828847B2 publication Critical patent/JPS5828847B2/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0−エチル−
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3・5−キシリル
N−メチルカーバメート(以下rXMcJ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 0-ethyl-
It is characterized by containing a mixture of 0-0-di(2,4-dichlorophenyl) phosphate (hereinafter referred to as "phosdaifen") and 3,5-xylyl N-methyl carbamate (hereinafter referred to as rXMcJ) as an active ingredient. This invention relates to a leafhopper control agent that exhibits resistance to carbamate insecticides.

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MMCとの混合物が抵抗性
ツマグロヨコバイに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, it was discovered that a mixture of phosdaifen and MMC exhibits a higher control effect on resistant leafhopper 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号公報において公知の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
度では殆んど殺虫活性を持たない。
Phosdaifen, a component of the mixture of the present invention, is
It is a known agricultural and horticultural fungicide as disclosed in Japanese Patent No. 20514, and it shows an excellent control effect particularly against blast disease, but it has almost no insecticidal activity at normal concentrations.

一方、MMCは、「農薬ハンドブック1976年版」の
第79〜80頁(日本植物防疫協会発行)などで既知の
殺虫剤であって、感受性ツマグロヨコバイには卓効を有
す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, MMC is an insecticide known from pages 79 to 80 of the "Pesticide Handbook 1976 Edition" (published by the Japan Plant Protection Association), and is highly effective against susceptible leafhoppers, but not sufficiently effective against resistant leafhoppers. No pest control effect can be obtained.

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, and at the same time becomes an effective agent against the same insect pests, it is also effective against pests such as brown-bottomed planthoppers, brown planthoppers, and stink bugs, as well as against blast disease. It also has the advantage of being effective and having 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。
Similar to widely used agricultural chemicals, the pesticidal agent according to the present invention is prepared by adding various auxiliary agents such as surfactants, dispersants, and wetting agents to a solid or liquid carrier to form powders or wettable powders. It can be used in formulations such as emulsions, granules, etc.

次に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される
ことはない。
Next, some examples of the present invention will be shown, but the types of adjuvants, amounts added, and 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、XMC25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 XMC, 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、MMC2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 MMC, 1 part of white carbon
1 part, 20 parts of talc, and 75 parts of clay are 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
ターンチーフル上でスプレーガンにて散布した。
Test Example 1 Resistant black leafhopper control effect test A diluted solution of a predetermined concentration of the emulsion prepared according to Example 1 was applied to potted rice plants at the 4th to 5th leaf stage at a rate of 1001 per 10 ares on a turnchill using a spray gun. did.

風乾した後稲茎葉部を切り取り直径2CrrL、長さ2
0CrrLの大きさの試験管に入れツマグロヨコバイ1
0頭を散失し24時間後に抑転虫数を調べた。
After air-drying, cut the rice stem leaves to a diameter of 2 CrrL and a length of 2
Put 1 leafhopper in a test tube with a size of 0 CrrL.
The number of suppressed insects was determined 24 hours after the disappearance of 0 insects.

試験は1濃度3区制で行い平均抑転虫率(%)求めた。The test was conducted using a 1-concentration, 3-area system, and the average insect suppression 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、期待値はブリス(Bliss)の式により求めた
Note that the expected value was determined using the Bliss formula.

第1表のケージに基づいて、カーペンタ−(Carpe
nt et al )の式によりLC5o(50%
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 cages in Table 1, Carpenter
LC5o (50%
The expected value (lethal drug concentration) was calculated, 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, synergistic dust 1 shows an additive effect, if it is smaller than 1, it shows an antagonistic effect, and if it is larger than ■, it shows 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.

7試1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時間煕明、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。
7 trials, 1 test example 2 Changes in susceptibility of 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 incubated at a constant temperature of 25°C for 16 hours. , sprouted rice plants were reared for generations under dark conditions for 8 hours, and then subjected to selection and rearing, and drug assays were conducted at any 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23cmX 30CTLX 21(17)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 23 cm x 30 CTL x 21 (17) plastic box, and the seedlings were raised to sprout. Rice was 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 is placed in a cage for breeding black leafhoppers, and approximately 1,000 adult black leafhoppers, which have been reared for generations, are 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時間後の生死重数を調査し
、LD、o値(μm/グ)を求めた。
In the drug test, the live and dead weight of adult female leafhoppers 3 to 4 days after emergence was investigated using a local application method after 24 hours, and the LD and o values (μm/g) were determined.

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

(註1) (註2) 淘汰前の岡山県産ツマグロヨコバイに対するMMCのL
D、。
(Note 1) (Note 2) L of MMC against black leafhopper from Okayama Prefecture before culling
D.

値は49.3μ2/グであった。無淘汰系のLD、。The value was 49.3μ2/g. Unselected LD.

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20世代後のLD5o
値(順に淘汰前、10回後、20回後の欄)を示す。
The value column shows the LD5o of the parent adult leafhopper, the 10th generation, and the 20th generation, which have been reared for generations without chemical selection.
The values (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3・5−キシリル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。
10-ethyl 0-0-di(2,4-dichlorophenyl)
A leafhopper control agent resistant to carbamate insecticides, characterized by containing a mixture of phosphate and 3,5-xylyl N-methyl carbamate as an active ingredient.
JP14544479A 1979-11-12 1979-11-12 Resistant leafhopper control agent Expired JPS5828847B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14544479A JPS5828847B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14544479A JPS5828847B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Publications (2)

Publication Number Publication Date
JPS5671014A JPS5671014A (en) 1981-06-13
JPS5828847B2 true JPS5828847B2 (en) 1983-06-18

Family

ID=15385367

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14544479A Expired JPS5828847B2 (en) 1979-11-12 1979-11-12 Resistant leafhopper control agent

Country Status (1)

Country Link
JP (1) JPS5828847B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0472270A (en) * 1990-07-09 1992-03-06 Mita Ind Co Ltd Sorter

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0472270A (en) * 1990-07-09 1992-03-06 Mita Ind Co Ltd Sorter

Also Published As

Publication number Publication date
JPS5671014A (en) 1981-06-13

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