JPS5828851B2 - Resistant leafhopper control agent - Google Patents

Resistant leafhopper control agent

Info

Publication number
JPS5828851B2
JPS5828851B2 JP14652379A JP14652379A JPS5828851B2 JP S5828851 B2 JPS5828851 B2 JP S5828851B2 JP 14652379 A JP14652379 A JP 14652379A JP 14652379 A JP14652379 A JP 14652379A JP S5828851 B2 JPS5828851 B2 JP S5828851B2
Authority
JP
Japan
Prior art keywords
control agent
resistant
leafhopper
rice
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
JP14652379A
Other languages
Japanese (ja)
Other versions
JPS5671018A (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 JP14652379A priority Critical patent/JPS5828851B2/en
Publication of JPS5671018A publication Critical patent/JPS5671018A/en
Publication of JPS5828851B2 publication Critical patent/JPS5828851B2/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−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」という)とS−Cα−(エト
キシカルボニル)ベンジルコジメチルホスホロチオロチ
オネート(以下「PAP」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 provides 0-ethyl-
〇-O-di(2,4-dichlorophenyl) phosphate (hereinafter referred to as "phosdaifen") and S-Cα-(ethoxycarbonyl)benzylcodimethylphosphorothiorothionate (hereinafter referred to as "PAP") as active ingredients. The present invention relates to a leafhopper control agent that is resistant to organophosphorus insecticides and carbamate insecticides, and is characterized by containing the following:

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 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PAP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, it was discovered that a mixture of phosdaifen and PAP exhibited a higher control effect on resistant leafhopper than expected from 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号公報において公知の農園
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 a known agricultural and horticultural fungicide as disclosed in Japanese Patent Publication No. 46-20514, and shows an excellent control effect against rice blast, but at a conventional concentration. It has no insecticidal activity.

一方PAPは、特公昭35−8250号公報において既
知の殺虫剤であって、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, PAP is an insecticide known from Japanese Patent Publication No. 35-8250, 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, as well as pests such as brown-bottomed planthoppers, brown-bottomed planthoppers, snail bugs, and stink bugs, as well as 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1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 used by adding various auxiliary agents such as surfactants, dispersants, and wetting agents to a carrier such as a liquid to formulate powders, wettable powders, single emulsion tablets, and the like.

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。実施例 1 (乳剤) ホスダイフェン25部、PAP25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)1
5部を混合して乳剤とする。
Note that all figures in the middle part of the examples indicate parts by weight. Example 1 (Emulsion) 25 parts of phosdaifen, 25 parts of PAP, 35 parts of xylene, and 1 part of Tulpol (emulsifier manufactured by Toho Chemical Industry Co., Ltd.)
Mix 5 parts to form an emulsion.

実施例 2 (粉剤) ※ ※ ホスダイフェン2部、PAP2部、ホワイトカーボ
ン1部、タルク20部及びフレーク5部を均一に混合粉
砕して粉剤を得る。
Example 2 (Powder) * * 2 parts of phosdaifen, 2 parts of PAP, 1 part of white carbon, 20 parts of talc and 5 parts of flakes are uniformly mixed and ground 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大きさが直径2cm、
長さ20射の試験管に入れツマグロヨコバイ10頭を散
失し24時間後に抑転重数を調べた。
After air-drying, cut out the leaves of the rice stalks to a size of 2 cm in diameter.
Ten black leafhoppers were dispersed in a test tube with a length of 20 shots, and the suppressed weight was determined 24 hours later.

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リンおよび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 and N-methyl carbamate insecticides.

本試験は1区10頭の3区制で行ない平均抑転虫率(%
)を求めた。
This test was conducted in three sections with 10 animals per section, and the average suppression 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LC50(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度を算
出した。
Based on the data in Table 1, Carpenter
LC50(5
The expected value (0% lethal drug concentration) was determined, and the degree of synergy of the insecticidal effect by mixing the active ingredients was calculated from the comparison with the actual value.

この場合、共力度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、1より大きい場合は相乗的効
果を示す。
In this case, a synergy of 1 indicates an additive effect, less than 1 indicates an antagonistic effect, and greater than 1 indicates a synergistic effect.

そして、共力度が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 degree of synergy 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クロヨコバイ個体群の感受性
の変化(岡山来意) 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 (from Okayama) The black leafhoppers used in the test were collected from a rice field in Kojima District, Okayama Prefecture, and then exposed to light for 16 hours at a constant temperature of 25°C for 8 hours. The sprouted rice plants were bred for generations under dark conditions, and were subsequently subjected to selection and breeding, and drug assays were conducted as needed.

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23CTLX 30CrnX 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。
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 plastic boxes measuring 23 CTL x 30 Crn x 2 cm, and sprouted rice plants were treated with the spray.

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fR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。
The sprouted rice was placed in a breeding cage for black leafhoppers, and approximately 1,000 black leafhopper fR insects were released, and 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. 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(μグ/り)を求めた。
For the drug test, the number of live and dead spots after 24 hours was investigated using a topical application method on adult female leafhoppers 3 to 4 days after emergence, and the LD5o value (μg/liter) was determined.

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s’−cα−(エトキシカルボニル)ベ
ンジルコジメチルホスホロチオ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。
10-ethyl 0-0-di(2,4-dichlorophenyl)
A leafhopper control agent resistant to organophosphorus insecticides and carbamate insecticides, characterized by containing phosphate and s'-cα-(ethoxycarbonyl)benzyl codimethyl phosphorothiolothionate as active ingredients.
JP14652379A 1979-11-14 1979-11-14 Resistant leafhopper control agent Expired JPS5828851B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14652379A JPS5828851B2 (en) 1979-11-14 1979-11-14 Resistant leafhopper control agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14652379A JPS5828851B2 (en) 1979-11-14 1979-11-14 Resistant leafhopper control agent

Publications (2)

Publication Number Publication Date
JPS5671018A JPS5671018A (en) 1981-06-13
JPS5828851B2 true JPS5828851B2 (en) 1983-06-18

Family

ID=15409569

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14652379A Expired JPS5828851B2 (en) 1979-11-14 1979-11-14 Resistant leafhopper control agent

Country Status (1)

Country Link
JP (1) JPS5828851B2 (en)

Also Published As

Publication number Publication date
JPS5671018A (en) 1981-06-13

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