JPH021802B2 - - Google Patents

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Publication number
JPH021802B2
JPH021802B2 JP56213906A JP21390681A JPH021802B2 JP H021802 B2 JPH021802 B2 JP H021802B2 JP 56213906 A JP56213906 A JP 56213906A JP 21390681 A JP21390681 A JP 21390681A JP H021802 B2 JPH021802 B2 JP H021802B2
Authority
JP
Japan
Prior art keywords
rice
parts
insecticidal
seedlings
leafhopper
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 - Lifetime
Application number
JP56213906A
Other languages
Japanese (ja)
Other versions
JPS58113110A (en
Inventor
Masayoshi Hirose
Kiminori Hirata
Ryoichi Nonaka
Yoshinori Ochiai
Tatsuo Takagaki
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.)
Nissan Chemical Corp
Original Assignee
Nissan Chemical Corp
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 Nissan Chemical Corp filed Critical Nissan Chemical Corp
Priority to JP56213906A priority Critical patent/JPS58113110A/en
Publication of JPS58113110A publication Critical patent/JPS58113110A/en
Publication of JPH021802B2 publication Critical patent/JPH021802B2/ja
Granted legal-status Critical Current

Links

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は2,3―ジヒドロ―2,2―ジメチル
―7―ベンゾフラニル〔(ジブチルアミノ)チオ〕
メチルカーボメート(以下カーボスルフアンと略
称する)と1,3―ジチオラン―2―イソデンマ
ロン酸ジイソプロピル(以下イソプロチオランと
略称する)とを有効成分として含有することを特
徴とする殺虫殺菌組成物に関するものである。 近年、水稲栽培において田植え時、稚苗、中苗
の機械移植が広範におこなわれている。 移植用苗は一般に60×30×3(cm)の育苗箱で
稚苗、中苗まで育て移植機にかけられて移植され
るが、移植前に粒剤または乳剤や水和剤等の水調
整液の殺虫剤あるいは殺菌剤が苗の根部に処理
(育苗箱施薬)され、根に薬剤を付着させた状態
で苗を機械移植し、水稲を水田初期害虫、例えば
ツマグロヨコバイ、ヒメトビウンカ、ハモグリバ
エ、イネドロオイムシ、イネミズゾウムシ、イネ
ゾウムシ等あるいはイモチ病の被害から保護して
いる。 このような栽培方法は、西南暖地における殺虫
剤抵抗性ツマグロヨコバイ常発地帯でも採用され
ているが、最近では従来使われてきた育苗箱施用
薬剤でも抵抗性の発達が認められている。 一般に有機リン剤やカーバメート剤に抵抗性の
発達したツマグロヨコバイを防除するために有機
リン剤とN―メチルカーバメート剤との相剰効果
を利用した混合粉剤等が水田に施用する場合、使
用されている。 育苗箱施薬においても同様な有機リン剤とN―
メチルカーバメート剤との混合物の相剰効果を利
用した適用方法が考えられるが、従来のN―メチ
ルカーバメートが育苗箱施薬においては水稲稚
苗、中苗に対し著しい薬害を引起すため育苗箱施
薬を不可能にしている。 一方、浸透性殺菌剤も機械移植する前に苗に施
用し水田でのイモチ病防除に効果を示している。
しかし、実際は育苗箱施用薬剤の殺虫剤と殺菌剤
がそれぞれ単剤で別個に同時施用され、田植時の
農繁期に多大の労力を要し、さらに育苗箱に多量
の薬剤を施用するため、機械移植時に薬剤が落下
し、害虫防除やイモチ病防除の効果が不均一とな
る弊害が生じている。 本発明者らは、水稲の稚苗、中苗に対する薬害
が通常の育苗箱施薬でほとんどなく、混合するこ
とにより抵抗性ツマグロヨコバイに対し顕著な相
剰効果をもたらし、更にイモチ病を防除し得る省
力化水稲育苗箱処理用殺虫殺菌組成物について研
究を重ねた結果、前記カーボスルフアンとイソプ
ロチオランとの混合が育苗箱施薬に使用できるこ
とを見出し本発明を完成した。 カーボスルフアンは特公昭53−39487号公報に
記載された化合物であり、双翅目害虫、鱗翅目害
虫、鞘翅目害虫、半翅目害虫、ハダニ等に対して
優れた殺虫活性を示す。 また、イソプロチオランは特公昭47−34126号
公報に記載されたジチオラン系化合物でいもち病
に対し防除効果を示し、また、トビイロウンカの
増殖抑制効果も示す。 本発明者らは、鋭意研究の結果カーボスルフア
ンとイソブチロチオランとを混合施用することに
より各単剤の有する殺虫特性からは予測し得ぬ優
れた相剰殺虫効果を発揮し、残効性も顕著に優れ
ることを見出した。 また、本発明組成物はイモチ病に対し、イソブ
チロチオラン単剤同様有効であつた。 更に、有用作物に対する薬害も生じないことか
ら安全性の面からも好適な殺虫殺菌剤といえる。 本発明に係る殺虫殺菌組成物は主にツマグロヨ
コバイ、ヒメトビウンカ、ハモグリバエ、イネド
ロオイムシ、イネゾウムシ、イネミズゾウムシ等
の水田初期害虫及びイモチ病に適用される場合が
多いが、他の農林作物を加害する病虫害に対して
も有用である。 本発明組成物を殺虫殺菌剤として施用するにあ
たつては、一般には適当な担体と混用して適用す
ることができ、所望により乳化剤、分散剤、懸濁
剤、浸透剤、展着剤、安定剤などを添加し乳剤、
水和剤、粉剤、粒剤、油剤等任意の剤型にて実用
に供することができる。この場合、有効成分であ
るカーボスルフインとイソプロチオランとの混合
割合は1:9〜9:1の範囲内で自由に決定する
ことができるが、好ましくは1:3〜3:1の範
囲である。 また、必要に応じて他種の殺ダニ剤、各種殺虫
剤、殺菌剤、植物生長調整剤、共力剤、誘引剤、
忌避剤、香料などを添加して使用することもでき
る。 次に、本発明の殺虫殺菌組成物の配合例の若干
を示すが、本発明はこれらのみに限定されるもの
ではない(以下の配合例中「部」は重量部を示
す)。 配合例 1 粒剤 カーボスルフアン 5部 イソプロチオラン 12部 破砕クレー 83部 カーボスルフアンとイソプロチオランを均一に
混合した後、この混合物を破砕クレーに均一に混
合させ粒剤を調整する。得られた粒剤は育苗箱当
り50〜100g施用するか、10a当り3〜6Kg散布
する。 配合例 2 乳剤 カーボスルフアン 10部 イソプロチオラン 20部 キシロール 60部 ソルポール2680(東邦化学商品名) 10部 以上を均一に混合して乳剤とする。使用に際し
ては、上記組成の乳剤を水で500〜2000倍に希釈
して100〜1000/10aを散布する。 配合例 3 水和剤 カーボスルフアン 20部 イソプロチオラン 40部 ジークライト 35部 ソルポール8048(東邦化学商品名) 3部 ルノツクス1000(東邦化学商品名) 2部 以上を均一に混合粉砕して水和剤とする。使用
に際しては、上記組成の水和剤を水で500〜2000
倍に希釈して50〜500/10aを散布する。 配合例 4 乳剤 カーボスルフアン 2.0部 イソプロチオラン 2.5部 タルク 95.5部 以上を均一に混合粉砕して粉剤とする。使用に
際しては、上記組成の粉剤を散粉機により3〜4
Kg/10aを散布する。 次に本発明組成物の有用性を試験例において具
体的に説明する。 試験例 1 抵抗性ツマグロヨコバイに対する殺虫試験 所定濃度の薬液をガラスビン(径5.5cm、高さ
6.5cm)に50ml入れ、穴のあいたコルク栓で蓋を
して稲苗をコルクの穴を通してたて、稲の根を薬
液に浸漬し、穴を綿でつめ、ガラス管をコルク栓
にたて、抵抗性ツマグロヨコバイ成虫(中川原系
統)を10頭放し、ふたをして25℃恒温室に保管し
て、放虫4日後の死虫数を調査し、殺虫率を算定
した。更にフイーニー(Finny)の簡易計算式を
用いて中央致死濃度(LC50)を求めた。更に、
中央致死濃度を用いてサン(Sun)法(J.Econ.
Entomol.,Vol.53.5p.887〜892.1960)により連合
毒性係数を求め、混合効果を評価した。結果を表
1に示す。
The present invention relates to 2,3-dihydro-2,2-dimethyl-7-benzofuranyl [(dibutylamino)thio]
This invention relates to an insecticidal and fungicidal composition characterized by containing methyl carbomate (hereinafter abbreviated as carbosulfan) and diisopropyl 1,3-dithiolane-2-isodenmalonate (hereinafter abbreviated as isoprothiolane) as active ingredients. be. In recent years, mechanical transplantation of young and medium-sized seedlings has been widely used during rice planting in wet rice cultivation. Seedlings for transplantation are generally grown to young or medium-sized seedlings in a 60 x 30 x 3 (cm) nursery box, and then placed in a transplanter and transplanted. The roots of the seedlings are treated with insecticides or fungicides (applied in a seedling box), and the seedlings are transplanted mechanically with the drug attached to the roots, and the paddy rice is infected with early-stage pests in the paddy field, such as leafhopper, brown leafhopper, leafminer fly, rice plant beetle, and rice weevil. , rice weevil, etc., or rice blast disease. This kind of cultivation method is also used in areas where insecticide-resistant leafhoppers are common in the warm southwestern regions, but recently the development of resistance has been observed even with the conventionally used chemicals applied in nursery boxes. In general, mixed powder agents that utilize the mutual effect of organic phosphorus agents and N-methyl carbamate agents are used when applied to rice fields to control black leafhopper, which has developed resistance to organic phosphorus agents and carbamate agents. . Similar organic phosphorus agents and N-
An application method that takes advantage of the synergistic effect of a mixture with a methyl carbamate agent is considered, but conventional N-methyl carbamate causes significant chemical damage to young and medium-sized paddy rice seedlings when applied in a nursery box, so it is difficult to use the conventional N-methyl carbamate when applied in a nursery box. making it impossible. On the other hand, systemic fungicides have also been applied to seedlings before mechanical transplantation and have shown effectiveness in controlling rice blast disease in rice fields.
However, in reality, the insecticide and fungicide used in the seedling box are applied separately and simultaneously, which requires a great deal of labor during the busy farming season for rice transplanting.Furthermore, since large amounts of chemicals are applied to the seedling box, mechanical transplantation is required. Sometimes, the chemicals fall down, resulting in uneven pest control and blast control effects. The present inventors have discovered that chemical damage to young and medium rice seedlings of paddy rice is almost non-existent when applied in a regular nursery box, and that by mixing the chemical, it has a remarkable mutual effect against resistant leafhopper, and furthermore, it is a labor-saving method that can control rice blast disease. As a result of repeated research on insecticidal and bactericidal compositions for treating paddy rice seedling boxes, it was discovered that a mixture of the carbosulfan and isoprothiolane can be used for seedling box treatment, and the present invention was completed. Carbosulfan is a compound described in Japanese Patent Publication No. 53-39487, and exhibits excellent insecticidal activity against Diptera pests, Lepidoptera pests, Coleoptera pests, Hemiptera pests, spider mites, etc. In addition, isoprothiolane is a dithiolane compound described in Japanese Patent Publication No. 47-34126 and exhibits a control effect against rice blast, and also exhibits an effect of inhibiting the growth of brown planthopper. As a result of extensive research, the present inventors have demonstrated that by applying a mixture of carbosulfan and isobutyrothiolane, an excellent synergistic insecticidal effect that could not be expected from the insecticidal properties of each single agent, and a residual effect. It was also found that the properties were significantly superior. Furthermore, the composition of the present invention was as effective against rice blast disease as isobutyrothiolane alone. Furthermore, since it does not cause any chemical damage to useful crops, it can be said to be a suitable insecticide and fungicide from the viewpoint of safety. The insecticidal and fungicidal composition of the present invention is mainly applied to paddy field early-stage pests such as leafhopper, brown leafhopper, leafminer fly, rice plant beetle, rice weevil, and rice water weevil, and to rice blast disease, but it is also used against pests that attack other agricultural and forestry crops. is also useful. When applying the composition of the present invention as an insecticidal fungicide, it can generally be mixed with a suitable carrier and, if desired, emulsifiers, dispersants, suspending agents, penetrating agents, spreading agents, etc. Emulsion by adding stabilizers etc.
It can be put to practical use in any form such as wettable powders, powders, granules, and oils. In this case, the mixing ratio of carbosulfin and isoprothiolane, which are active ingredients, can be freely determined within the range of 1:9 to 9:1, but is preferably within the range of 1:3 to 3:1. . In addition, other types of acaricides, various insecticides, fungicides, plant growth regulators, synergists, attractants,
It is also possible to add repellents, fragrances, etc. Next, some formulation examples of the insecticidal and fungicidal composition of the present invention will be shown, but the present invention is not limited to these ("parts" in the following formulation examples indicate parts by weight). Formulation Example 1 Granule Carbosulfan 5 parts Isoprothiolane 12 parts Crushed clay 83 parts After uniformly mixing carbosulfan and isoprothiolane, this mixture is uniformly mixed with crushed clay to prepare granules. The obtained granules are applied in an amount of 50 to 100 g per seedling box, or 3 to 6 kg per 10 acres. Formulation Example 2 Emulsion Carbosulfan 10 parts Isoprothiolane 20 parts Xylol 60 parts Solpol 2680 (Toho Chemical brand name) 10 parts Mix the above ingredients uniformly to make an emulsion. In use, the emulsion having the above composition is diluted 500 to 2000 times with water and then sprayed at 100 to 1000/10a. Formulation example 3 Wettable powder Carbosulfan 20 parts Isoprothiolane 40 parts Siegrite 35 parts Solpol 8048 (Toho Chemical brand name) 3 parts Lunox 1000 (Toho Chemical brand name) 2 parts Mix and grind the above uniformly to form a wettable powder. do. When using, mix the hydrating agent with the above composition with water at a concentration of 500 to 2000.
Dilute it twice and spray 50-500/10a. Formulation Example 4 Emulsion Carbosulfan 2.0 parts Isoprothiolane 2.5 parts Talc 95.5 parts Mix and grind the above ingredients uniformly to make a powder. When using, powder of the above composition is mixed with a duster for 3 to 4 minutes.
Spray Kg/10a. Next, the usefulness of the composition of the present invention will be specifically explained using test examples. Test example 1 Insecticidal test against resistant leafhopper A chemical solution of a specified concentration was placed in a glass bottle (diameter 5.5 cm, height
Pour 50 ml into a 6.5 cm) container, cover with a cork stopper, put rice seedlings through the hole in the cork, soak the rice roots in the chemical solution, plug the hole with cotton, and put a glass tube into the cork stopper. Ten resistant leafhopper adults (Nakagawara strain) were released and stored in a constant temperature room at 25°C with a lid on.The number of dead insects was counted 4 days after release, and the killing rate was calculated. Furthermore, the median lethal concentration (LC 50 ) was determined using Finny's simple calculation formula. Furthermore,
The Sun method (J.Econ.
Entomol., Vol.53.5p.887-892.1960), the combined toxicity coefficient was determined and the mixed effect was evaluated. The results are shown in Table 1.

【表】 表1に示す如く、本発明組成物は各単剤より優
れた浸透殺虫活性を示し、また強力な相剰効果を
示した。 試験例 2 育苗箱施薬による抵抗性ツマグロヨコバイに対
する残効性と稲に対する薬害試験 育苗箱に慣行通り水稲稚苗を栽培し、(品種:
日本晴)、播種21日後(移植当日)、供試粒剤を育
苗箱当り70g処理し、その後ジヨロにて充分潅水
し、施薬2時間後に10000分の1アールポツト
(土を入れ水を加え水田状態とした)に育苗箱か
らかきとつた苗(土をつけたまま)をポツト当り
5本ひと株にして移植した。所定日ごとにポツト
は金網円筒で覆い、抵抗性ツマグロヨコバイ成虫
(中川原系統)を10頭/ポツト放虫し、48時間後
の死虫数を調査し、死虫率を求めた。更に薬害調
査用も同様に作成し、移植後経過日数に応じて莖
葉の性状、草丈を調査した。いずれも1区3連制
で行なつた。表に結果を示す。
[Table] As shown in Table 1, the composition of the present invention exhibited superior systemic insecticidal activity to each agent alone, and also exhibited a strong synergistic effect. Test example 2 Residual efficacy against resistant black leafhopper and chemical damage test on rice by applying chemicals in a nursery box Paddy rice seedlings were cultivated in a nursery box as usual, and (variety:
Nipponbare), 21 days after sowing (on the day of transplanting), 70g of test granules were applied to each seedling box, and then thoroughly watered with water. Two hours after application, a 1/10,000-are pot (filled with soil and water was added to create a paddy field condition). The seedlings (with soil still attached) that had been scraped out of the seedling box were transplanted into the pot (with the soil still attached), with 5 plants per pot. Every designated day, the pot was covered with a wire mesh cylinder and 10 adult resistant leafhoppers (Nakagawara strain) were released per pot.The number of dead insects was counted after 48 hours to determine the mortality rate. Furthermore, a sample for chemical damage investigation was prepared in the same manner, and the properties of the pod leaves and plant height were investigated according to the number of days that had passed since transplantation. Both races were held in three consecutive races in one ward. The results are shown in the table.

【表】 表2に示すように本発明組成物は抵抗性ツマグ
ロヨコバイに対して優れた残効性を示し、また稲
に対し薬害を示さなかつた。 試験例 3 育苗箱施薬による稲いもち病に対する防除効果
試験 試験例2と同様に作成したポツト植稲をガラス
室に保管し、移植後経過日数に応じて稲いもち病
菌胞子を噴霧接種した。接種7日後にポツト当り
のいもち病斑数を調査し、下記の基準で防除価を
求めた。その結果を表3に示す。 防除価=(無処理区病斑数−処理区病斑数/無処理区
病斑数) ×100
[Table] As shown in Table 2, the composition of the present invention exhibited excellent residual efficacy against resistant leafhopper and did not cause any chemical damage to rice. Test Example 3 Test of the control effect of rice blast disease using seedling box application Rice grown in pots as in Test Example 2 was stored in a glass room, and rice blast fungus spores were sprayed and inoculated according to the number of days that had passed since transplantation. Seven days after inoculation, the number of rice blast lesions per pot was investigated, and the control value was determined using the following criteria. The results are shown in Table 3. Control value = (Number of lesions in untreated area - Number of lesions in treated area / Number of lesions in untreated area) × 100

【表】 表3に示す如く、本発明組成物は稲いもち病に
対し、すぐれた防除効果を発揮した。
[Table] As shown in Table 3, the composition of the present invention exhibited an excellent control effect against rice blast.

Claims (1)

【特許請求の範囲】 1 2,3―ジヒドロ―2,2―ジメチル―7―
ベンゾフラニル〔(ジブチルアミノ)チオ〕メチ
ルカーバメートと1,3―ジチオラン―2―イソ
デンマロン酸ジイソプロピルとを有効成分として
含有することを特徴とする殺虫殺菌組成物。
[Claims] 1 2,3-dihydro-2,2-dimethyl-7-
An insecticidal and fungicidal composition comprising benzofuranyl[(dibutylamino)thio]methyl carbamate and diisopropyl 1,3-dithiolane-2-isodenmalonate as active ingredients.
JP56213906A 1981-12-26 1981-12-26 Insecticidal and fungicidal composition Granted JPS58113110A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56213906A JPS58113110A (en) 1981-12-26 1981-12-26 Insecticidal and fungicidal composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56213906A JPS58113110A (en) 1981-12-26 1981-12-26 Insecticidal and fungicidal composition

Publications (2)

Publication Number Publication Date
JPS58113110A JPS58113110A (en) 1983-07-05
JPH021802B2 true JPH021802B2 (en) 1990-01-12

Family

ID=16646976

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56213906A Granted JPS58113110A (en) 1981-12-26 1981-12-26 Insecticidal and fungicidal composition

Country Status (1)

Country Link
JP (1) JPS58113110A (en)

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5167725A (en) * 1974-12-03 1976-06-11 Nihon Nohyaku Co Ltd SATSUCHUYOSOSEIBUTSU
JPS5339487A (en) * 1976-09-22 1978-04-11 Hitachi Cable Ltd Production method of power cable
JPS5585505A (en) * 1978-12-22 1980-06-27 Nippon Nohyaku Co Ltd Insecticide composition

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5167725A (en) * 1974-12-03 1976-06-11 Nihon Nohyaku Co Ltd SATSUCHUYOSOSEIBUTSU
JPS5339487A (en) * 1976-09-22 1978-04-11 Hitachi Cable Ltd Production method of power cable
JPS5585505A (en) * 1978-12-22 1980-06-27 Nippon Nohyaku Co Ltd Insecticide composition

Also Published As

Publication number Publication date
JPS58113110A (en) 1983-07-05

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