JPS63201104A - Herbicide composition - Google Patents

Herbicide composition

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Publication number
JPS63201104A
JPS63201104A JP62032385A JP3238587A JPS63201104A JP S63201104 A JPS63201104 A JP S63201104A JP 62032385 A JP62032385 A JP 62032385A JP 3238587 A JP3238587 A JP 3238587A JP S63201104 A JPS63201104 A JP S63201104A
Authority
JP
Japan
Prior art keywords
compound
weeds
herbicide
herbicidal
effect
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.)
Pending
Application number
JP62032385A
Other languages
Japanese (ja)
Inventor
Hideo Morinaka
秀夫 森中
Mitsuyuki Murakami
充幸 村上
Kazuaki Tsukuda
和明 佃
Naoki Miyamura
直樹 宮村
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.)
Tosoh Corp
Original Assignee
Tosoh 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 Tosoh Corp filed Critical Tosoh Corp
Priority to JP62032385A priority Critical patent/JPS63201104A/en
Publication of JPS63201104A publication Critical patent/JPS63201104A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide a herbicide composition containing one or two kinds of O-3-t- or O-4-t-butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate in combination with bromobutide and pyrazoxyfen as active components. CONSTITUTION:The objective herbicide contains (A) O-3-tert-butylphenyl N-(6- methoxy-2-pyridyl)-N-methylthiocarbamate and/or O-4-tert-butylphenyl N-(6- methoxy-2-pyridyl)-N-methylthiocarbamate, (B) bromobutide [N-(alpha,alpha-dimethyl benzyl)-2-bromo-3,3-dimethylbutylamide] and (C) pyrazoxyfen [4-(2,4- dichlorobenzoyl)-1,3-dimethyl-5-phenacyloxypyrazole] as active components. The composition has excellent herbicidal effect and high safety to paddy rice plant and exhibits synergistic effect.

Description

【発明の詳細な説明】 (産業上の利用分野〕 本発明は除草剤組成物に関し、詳しくは0−3−jer
t−ブチルフェニル N−(6−メトキシ−2−ピリジ
ル)−N−メチルチオカーバメートまたは0−4−te
rt−ブチルフェニル N−(6−メトキシ−2−ピリ
ジル)−N−メチルチオカーバメートの1種または2種
と、N−(α、α−ジメチルベンジル)−2−ブロモー
3,3〜ジメチルブチルアミドおよび4−(2,4−ジ
クロロベンゾイル)−1,3−ジメチル−5−フェナシ
ルオキシピラゾールとを有効成分として含有することを
特徴とする、除草効果の優れた除草剤組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Field of Application) The present invention relates to a herbicide composition, and more specifically
t-Butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate or 0-4-te
rt-butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate or two, N-(α,α-dimethylbenzyl)-2-bromo 3,3-dimethylbutyramide and The present invention relates to a herbicidal composition with excellent herbicidal effects, characterized by containing 4-(2,4-dichlorobenzoyl)-1,3-dimethyl-5-phenacyloxypyrazole as an active ingredient.

〔従来の技術〕[Conventional technology]

稲作用の除草剤について既に多数のものが開発されてい
るが、その性能、安全性の向上および薬害の軽減に対す
る市場の要望は、依然として強いものがある。
Although a large number of herbicides for rice cultivation have already been developed, there is still strong market demand for improved performance, safety, and reduction of chemical damage.

また水田雑草の特徴として、その多くは発生時期が一敗
せず、長期にわたって発生すると共に、除草剤散布時に
おける雑草の生育状態も、発芽前のものからある程度生
育の進んだものまで各種発前段階のものが混在している
のが常である。このため、除草剤を一回散布しただけで
は満足すべき除草効果を得ることができず、数回にわた
り除草剤を施用しなければならない。
In addition, many of the weeds in paddy fields are characterized by their emergence over a long period of time, and the growth conditions of the weeds at the time of herbicide application vary from those that have not yet germinated to those that have grown to some extent. There is usually a mixture of stages. For this reason, it is not possible to obtain a satisfactory herbicide effect by spraying the herbicide only once, and the herbicide must be applied several times.

〔発明が解決しようとする問題点〕[Problem that the invention seeks to solve]

本発明者らは、低薬量の薬剤を散布するだけで発芽前の
ものからある程度生育の進んだ雑草までほぼ完全に防除
し、長期間その効果を持続し、かつ水稲に対する安全性
が高い優れた除草剤を開発すべく鋭意研究を重ねた結果
、本発明の除草剤組成物が、各有効成分を適切な割合で
混合施用することにより、予想を大きく上まわる極めて
顕著な相乗効果が得られることを見出し、本発明を完成
した。
The present inventors have developed an excellent product that can almost completely control weeds from pre-germination to weeds that have grown to some extent by simply spraying a low dose of the chemical, maintains its effect for a long time, and is highly safe for paddy rice. As a result of intensive research aimed at developing herbicides, we have found that the herbicide composition of the present invention has an extremely significant synergistic effect that far exceeds expectations by applying each active ingredient in an appropriate proportion. They discovered this and completed the present invention.

〔問題点を解決するための手段〕[Means for solving problems]

本発明の除草w1組成物は、除草効果が優れ、かつ水稲
に対する安全性が高いもので、各有効成分が単独で示す
除草効果からは予想できない優れた相乗効果を有してい
る。
The herbicidal w1 composition of the present invention has an excellent herbicidal effect and is highly safe for paddy rice, and has an excellent synergistic effect that cannot be expected from the herbicidal effects of each active ingredient alone.

すなわち本発明は、0−3−tart−ブチルフェニル
 N−(6−メトキシ−2−ピリジル)−N−メチルチ
オカーバメート(以下、化合物■という、)または0−
4−tart−ブチルフェニル N−(6−メトキシ−
2−ピリジル)−N−メチルチオカーバメート(以下、
化合物■という、)の1種または2種と、N−(α、α
−ジメチルベンジル)−2−プロモー3.3−ジメチル
ブチルアミド(以下、化合物■という、)および4−(
2,4−ジクロロベンゾイル)−1,3−ジメチル−5
−フェナシルオキシピラゾール(以下、化合物■という
、)を有効成分として含有することを特徴とする除草剤
組成物を提供するものである。
That is, the present invention provides 0-3-tart-butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate (hereinafter referred to as compound ①) or 0-
4-tart-butylphenyl N-(6-methoxy-
2-pyridyl)-N-methylthiocarbamate (hereinafter referred to as
One or two types of compounds (referred to as compound ■) and N-(α, α
-dimethylbenzyl)-2-promo 3,3-dimethylbutyramide (hereinafter referred to as compound ■) and 4-(
2,4-dichlorobenzoyl)-1,3-dimethyl-5
The present invention provides a herbicidal composition containing -phenacyloxypyrazole (hereinafter referred to as compound (2)) as an active ingredient.

〔作用〕[Effect]

化合物!または化合物■を単独で水田用除草剤として使
用すると、雑草発芽前の段階ではノビエ。
Compound! Alternatively, when compound ■ is used alone as a herbicide for paddy fields, weeds grow in the pre-emergence stage.

タマガヤツリ、コナギ、キカシグサ等に卓効を示し、さ
らにホタルイ等に対しても有効である。特にノビエに対
しては、発芽後ある程度生育が進んだものに対しても除
草効果を有しており、しかも移植水稲に対しては実用上
薬害が認められない点がこの薬剤の大きな特徴である。
It is highly effective against Japanese snails, Japanese snails, and other insects, and is also effective against fireflies, etc. The major feature of this drug is that it has a herbicidal effect on weeds, even those that have grown to a certain extent after germination, and there is no practical harm to transplanted paddy rice. .

しかしながら、特に雑草の生育期において一部の多年生
雑草に対しては除草効果が充分ではない。
However, the herbicidal effect is not sufficient against some perennial weeds, especially during the weed growing season.

一方、化合物mは一船名をブロモブチドと言い、単独で
水田用除草剤として使用した場合、雑草の発生前から発
生直後までの処理で、ホタルイ、タマガヤツリおよびマ
ツバイに卓効を示し、さらにノビエ、コナギ、キカシグ
サ、ミズガヤツリ等に対しても有効である。しかも水稲
に対して安全性が高く、水田用除草剤として有用性が大
きい、しかし、雑草の生育がある程度進むと、除草効果
が弱くなり、特に生育期のノビエに対しては除草効果は
不充分である。
On the other hand, Compound M is called bromobutide, and when used alone as a herbicide for paddy fields, it is highly effective against firefly, Japanese cypress, and Japanese grasshopper when treated from before to immediately after the emergence of weeds. It is also effective against grasshoppers, staghorn snails, water snails, etc. Moreover, it is highly safe for paddy rice, and is highly useful as a herbicide for paddy fields. However, once the weeds have grown to a certain extent, the weeding effect becomes weaker, and the weeding effect is particularly insufficient against grasshoppers during the growing season. It is.

また、化合物■は一船名をビラジキシフェンと言い、単
独で水田用除草剤として使用した場合、雑草の発生前か
ら発生直後までの処理で、−年生雑草ばかりでなく多年
生雑草のウリカワに対して高い除草効果を示す、さらに
ホタルイ、ミズガヤツリ等に対しても有効である。しか
も水稲に対して安全性が高く、水田用除草剤として有用
性が大きい、しかしながら、雑草の生育がある程度進む
と除草効果が弱くなり、特に生育期のノビエに対しては
除草効果は期待できない。
In addition, the compound ■, whose name is biradixifen, is used alone as a herbicide for paddy fields, and when treated from before to just after the emergence of weeds, it is highly effective against not only annual weeds but also perennial weeds. It exhibits a herbicidal effect and is also effective against firefly, water snail, etc. Moreover, it is highly safe for paddy rice, and is highly useful as a herbicide for paddy fields.However, once the weeds have grown to a certain extent, the herbicidal effect becomes weaker, and the herbicidal effect cannot be expected, especially against wild grass during the growing season.

化合物■または化合物■の1種または2種と化合物mお
よび化合物■とを配合した本発明の除草剤組成物がそれ
ぞれの薬剤の短所を相い補うだけでなく、極めて顕著な
相乗効果を示すことは全く予想外のことであった。
The herbicidal composition of the present invention, which is a combination of compound (1) or one or both of compound (2) and compound (m) and compound (2), not only compensates for the shortcomings of each drug, but also exhibits an extremely significant synergistic effect. was completely unexpected.

本発明の除草剤組成物の各有効成分の配合割合は特に1
11@はな(、広い配合比において優れた相乗効果が得
られるが、好ましくは化合物■または化合物■の1種ま
たは2種の1重量部に対して化合物■は0.1−10重
量部程度および化合物■は0.1−10重量部程度が適
当である。
The blending ratio of each active ingredient in the herbicide composition of the present invention is particularly 1
11@Hana (Excellent synergistic effects can be obtained in a wide range of blending ratios, but preferably Compound ■ is about 0.1 to 10 parts by weight per 1 part by weight of Compound ■ or one or two of Compound ■. Appropriately, about 0.1 to 10 parts by weight of Compound (1) and Compound (2) are used.

本発明の除草剤組成物を実際に使用する場合には、化合
物!または化合物■の1種または2種と、化合物Iおよ
び化合物■とのそれぞれの適当量を不活性担体と混合し
、通常の農薬使用形態である粒剤、微粒剤、水和剤、乳
剤、粉剤、フロアブル剤等の種々の形にして使用するこ
とができる。
When actually using the herbicide composition of the present invention, the compound! Alternatively, one or two of Compound (2), Compound I and Compound (2) may be mixed in appropriate amounts with an inert carrier to form granules, fine granules, wettable powders, emulsions, and powders, which are commonly used forms of agricultural chemicals. It can be used in various forms such as , flowable agents, etc.

固体担体としては、炭酸カルシウム、リン灰石。Solid carriers include calcium carbonate and apatite.

石こう、シリカゲル、バーミキュライト、雲母。Gypsum, silica gel, vermiculite, mica.

ケイソウ土、タルク、パイロフェライト、酸性白土、ク
レー、カオリナイト、モンモリロナイト。
Diatomaceous earth, talc, pyroferrite, acid clay, clay, kaolinite, montmorillonite.

ベントナイト、ホワイトカーボン、軽石粉等の鉱物性粉
末、結晶性セルロース、デンプン等の植物性粉末、ポリ
塩化ビニール、石油樹脂等の高分子化合物等を挙げるこ
とができる。
Examples include mineral powders such as bentonite, white carbon, and pumice powder, vegetable powders such as crystalline cellulose and starch, and polymeric compounds such as polyvinyl chloride and petroleum resins.

液体担体としては、メタノール、エタノール。Liquid carriers include methanol and ethanol.

シクロヘキサノール、アミルアルコール8エチレングリ
コール等のアルコール類、ベンゼン、トルエン、キシレ
ン、メチルナフタレン等の芳香族炭化水素類、イソホロ
ン、シクロヘキサノン等のケトン類、クロロベンゼン、
トリクロロエチレン等のハロゲン化炭化水素類、エチル
セロソルブ、ブチルセロソルブ、ジオキサン等のエーテ
ル類、酢酸イソプロピル、酢酸ベンジル等のエステル類
、ジメチルホルムアミド、ジメチルスルホキシド等の極
性溶媒類、ケロシン、鉱油、水等を挙げることができる
Alcohols such as cyclohexanol, amyl alcohol 8 ethylene glycol, aromatic hydrocarbons such as benzene, toluene, xylene, methylnaphthalene, ketones such as isophorone, cyclohexanone, chlorobenzene,
Examples include halogenated hydrocarbons such as trichloroethylene, ethers such as ethyl cellosolve, butyl cellosolve, and dioxane, esters such as isopropyl acetate and benzyl acetate, polar solvents such as dimethylformamide and dimethyl sulfoxide, kerosene, mineral oil, and water. Can be done.

さらに製剤上必要ならば、界面活性剤、展着剤。In addition, surfactants and spreading agents may be added if necessary for the formulation.

結合剤等の農薬に使用される補助剤を、あるいは安定剤
を混合することにより、除草効果の確実性を高めること
もできる。
The reliability of the herbicidal effect can be increased by adding adjuvants used in agricultural chemicals such as binders or stabilizers.

また、本発明の除草剤組成物は、必要に応じて殺虫剤、
殺菌剤、植物成長調節剤、肥料、あるいは他の除草剤を
含をしてもよく、またこれらのものと併用することもで
きる。
In addition, the herbicide composition of the present invention may optionally contain an insecticide,
It may also contain or be used in combination with fungicides, plant growth regulators, fertilizers, or other herbicides.

本発明の除草剤組成物を調製する際の各有効成分の配合
量は、適用場面、施用時期、施用方法。
The amount of each active ingredient when preparing the herbicide composition of the present invention depends on the application situation, application time, and application method.

対象草種等により異なるが、1アール当たりの有効成分
量で、化合物!または化合物■は一般的には1−=50
 g、好ましくは2〜30gであり、化合物■は一般的
には1〜50g、好ましくは2〜30gであり、化合物
■は一般的には1〜50g1好ましくは2〜30gの範
囲が適当である。
Although it varies depending on the target grass species, etc., the amount of active ingredient per are is a compound! Or compound ■ is generally 1-=50
g, preferably 2 to 30 g, Compound (1) is generally 1 to 50 g, preferably 2 to 30 g, and Compound (2) is generally 1 to 50 g, preferably 2 to 30 g. .

また総有効成分量は、一般的には1アール当たり5〜1
00g、好ましくは10〜60gの範囲が適当である。
In addition, the total amount of active ingredients is generally 5 to 1 per are.
00g, preferably in the range of 10 to 60g.

製剤における総有効成分の含有率は、重量比で−a的に
は1〜90%、好ましくは3〜80%の範囲が適当であ
る。
The content of the total active ingredients in the preparation is suitably in the range of 1 to 90%, preferably 3 to 80% in terms of weight ratio.

〔実施例〕〔Example〕

次に本発明除草剤組成物の製剤の実施例を説明するが、
本発明はこれらのみに限定されるものではない、実施例
中、「部」は重量部を示す。
Next, examples of formulations of the herbicide composition of the present invention will be explained.
The present invention is not limited to these. In the examples, "parts" indicate parts by weight.

実施例1 化合物1          10部 化合物I11          10部化合物IV 
          15部ケイソウ±       
  61部 ネオペレックス 〔商品名:花王アトラス員製〕  2部ツルポール80
0A 〔商品名:東邦化学工業■製〕 2部 上記成分を混合粉砕して、水和剤を得た。
Example 1 Compound 1 10 parts Compound I11 10 parts Compound IV
Part 15 Keiso±
61 parts Neoperex [Product name: Kao Atlas Co., Ltd.] 2 parts Tsurupol 80
0A [Product name: manufactured by Toho Chemical Industry ■] Two parts of the above components were mixed and ground to obtain a wettable powder.

実施例2 化合物!           3部 化合物■           2部 化合物■           5部 化合物■           7部 ツルポール800A      10部キシレン   
       73部 上記成分を混合溶解して、乳剤を得た。
Example 2 Compound! 3-part compound ■ 2-part compound ■ 5-part compound ■ 7-part Tsurpol 800A 10-part xylene
73 parts The above components were mixed and dissolved to obtain an emulsion.

実施例3 化合物■           4部 化合物m            s部化合物■   
        5部 ベントナイト        35部 タルク           48部 ツルポール800A       3部上記成分を混合
粉砕した後、適量の水を加えて混練し、直径0.7fi
の篩穴から押し出し、乾燥後1〜’1mの長さに切断し
て粒剤を得た。
Example 3 Compound ■ 4-part compound m S-part compound ■
5 parts bentonite 35 parts talc 48 parts Tsurupol 800A 3 parts After mixing and pulverizing the above ingredients, add an appropriate amount of water and knead to obtain a diameter of 0.7 fi.
The mixture was extruded through a sieve hole, dried, and then cut into pieces of 1 to 1 m in length to obtain granules.

次に、本発明の除草剤組成物の優れた除草効果を実施例
および比較例により説明する。
Next, the excellent herbicidal effect of the herbicide composition of the present invention will be explained using Examples and Comparative Examples.

実施例4および比較例 直径211のプラスチック容器に、水を加えて代かき状
態にした水田土壌を入れ、土壌表層に各種雑草の種子を
播種し、催芽させたミズガヤツリおよびウリカワの塊茎
を移植し、さらに2葉期の水稲苗(品種:日本晴)を1
1の深さに2本2株植えとした。その後’1cm湛水し
、温室内に静置した。水稲移植3日後(ノビエ発芽前)
および水稲移植10日後(ノビエ2葉期)に、前記実施
例3に示した方法に準じて調製した、本発明除草剤組成
物の校則の所定量を、手で散布処理した。その後温室内
に静置し、適時散水した。薬剤の処理3週間後に、除草
効果および水稲の薬害について調査した。水稲移植3日
後処理の結果を第1表に、水稲移植10日後処理の結果
を第2表に示した。
Example 4 and Comparative Examples Paddy soil that had been made into a paddy field by adding water was placed in a plastic container with a diameter of 211 cm, seeds of various weeds were sown on the soil surface layer, and the germinated tubers of Cyperus japonica and Urikava were transplanted. 1 paddy rice seedling (variety: Nipponbare) at the two-leaf stage
Two plants were planted at a depth of 1. Thereafter, it was submerged with water to a depth of 1 cm and left in a greenhouse. 3 days after transplanting paddy rice (before germination of wildflowers)
Then, 10 days after transplanting paddy rice (two-leaf field stage), a predetermined amount of the herbicide composition of the present invention, prepared according to the method shown in Example 3, as specified in the school regulations, was sprayed by hand. The plants were then placed in a greenhouse and watered at appropriate times. Three weeks after the chemical treatment, the herbicidal effect and damage to paddy rice were investigated. Table 1 shows the results of the treatment 3 days after rice transplantation, and Table 2 shows the results of the treatment 10 days after rice transplantation.

なお、第1表および第2表において「薬量」は、有効成
分量を水田1アール当たりの量に換算した値を示す。
In addition, in Tables 1 and 2, "drug amount" indicates a value obtained by converting the amount of active ingredient into the amount per 1 are of paddy field.

除草効果および薬害の評価は下記の基準に従い判定した
Evaluation of herbicidal effect and phytotoxicity was made according to the following criteria.

除草効果判定基準     薬害判定基準10100%
防除     −二無 害9: 90%防除     
士:?X1小害8: 80%防除     +:小 害
7: 70%防除     +:中 害6: 60%防
除     +1+二大 害5: 50%防除    
 ×:枯 死4: 40%防除 3: 30%防除 2: 20%防除 1: 10%防除 0:  0%防除 比較例として各有効成分化合物を単独で、あるいは混合
して上記実施例と同様に処理した場合および無処理区の
、除草効果および薬害の評価も上記基準に従って調査判
定し、各表中に示した。
Weeding effect determination criteria Chemical damage determination criteria 10100%
Pest control - 2 no Harm 9: 90% control
Master:? X1 Minor damage 8: 80% control +: Small Harm 7: 70% control +: Medium Harm 6: 60% control +1 + 2 Major damage 5: 50% control
×: Blight 4: 40% control 3: 30% control 2: 20% control 1: 10% control 0: 0% control As a comparative example, each active ingredient compound was used alone or in combination in the same manner as in the above example. Evaluations of herbicidal effects and phytotoxicity in treated and untreated plots were also conducted according to the above criteria and are shown in each table.

本発明によってもたらされた各活性化合物の優れた相乗
効果は、実施例4の結果から既に明白であるが、さらに
代表車種として難防除雑草の一つであるミズガヤツリを
用いて更に詳しく説明する。
Although the excellent synergistic effect of each active compound brought about by the present invention is already clear from the results of Example 4, it will be further explained in more detail using Cyperus japonica, which is one of the difficult-to-control weeds, as a representative species.

三種の活性化合物の相互作用を検定する方法として、ウ
ィーズ154’、20〜22頁、1967年に記載のあ
るコルビイ (Colby)の計算式が通常用いられる
。すなわち、 ただし、 X−化合物aをpg/a用いた時の除草効果(χ)Y−
化合物すをqg/a用いた時の除草効果(χ)Z−化合
物Cをr g/a用いた時の除草効果(χ)E=a、b
、cをそれぞれp+q、rg/a混用した時に予想され
る除草効果(χ) 実際に測定された除草効果(%)の値がEを上まわれば
、その組成物には相乗作用が存在することを示している
As a method for assaying the interaction of three active compounds, the Colby formula described in Weeds 154', pp. 20-22, 1967 is usually used. That is, however, the herbicidal effect (χ) when X-compound a is used in pg/a Y-
Herbicidal effect (χ) when compound C is used at qg/a Z-Herbicidal effect (χ) when compound C is used at rg/a E=a, b
, c is the expected herbicidal effect (χ) when p+q and rg/a are mixed, respectively. If the value of the actually measured herbicidal effect (%) exceeds E, it means that the composition has a synergistic effect. It shows.

以下、本発明の除草剤組成物の相互作用の検定試験とそ
の結果を実施例で示す。
EXAMPLES Hereinafter, the interaction test of the herbicide composition of the present invention and its results will be shown in Examples.

実施例5 面積1 B 36cd (31x56cm)のプラスチ
ック容器に代かき状態の水田土壌を底から7cmの深さ
まで入れ、これにミズガヤツリの塊茎10個を移植した
。翌日33の湛水を行い、温室内にて育成した。移植7
日後に、前記実施例3に準じて調製した本発明除草剤組
成物および各存効成分化合物単独の粒剤の所定量を、手
で散布処理した。その後温室内に静置し、適時散水した
Example 5 A plastic container with an area of 1 B 36 cd (31 x 56 cm) was filled with paddy soil in a paddy state to a depth of 7 cm from the bottom, and 10 tubers of Cyperus japonica were transplanted into the container. The next day, the plants were flooded with water for 33 days and grown in a greenhouse. transplant 7
After a day, a predetermined amount of granules containing the herbicide composition of the present invention prepared according to Example 3 and each existing active ingredient compound alone were sprayed by hand. The plants were then placed in a greenhouse and watered at appropriate times.

薬剤処理30日後に、残存ミズガヤツリ茎葉部を切り取
って集め、風乾重を測定して以下の式により除草効果を
算出し、その結果を第3表に示した。
After 30 days of chemical treatment, the remaining stems and leaves of Cyperus japonica were cut and collected, the air dry weight was measured, and the herbicidal effect was calculated using the following formula, and the results are shown in Table 3.

除草効果(χ)= (無処理区の風乾重) 第3表 、〔発明の効果〕 第1表、第2表および第3表から明らかなように、本発
明の除草剤組成物は、各を効成分単独施用の場合に比較
して段車力が著しく増強されている。これは各有効成分
間の共力作用によるものであり、顕著な相乗作用がある
と認められる。
Herbicidal effect (χ) = (air dry weight of untreated area) Table 3, [Effect of the invention] As is clear from Tables 1, 2, and 3, the herbicidal composition of the present invention Compared to the case where the active ingredient is applied alone, the plate force is significantly enhanced. This is due to the synergistic effect between each active ingredient, and it is recognized that there is a significant synergistic effect.

すなわち本発明の除草剤組成物の最大の特徴として、各
有効成分が単独で示す除草効果からは予想できなかった
低薬量同士の組み合わせで、多くの雑草に対して高い除
草効果を得ることができる点を挙げることができる。
In other words, the greatest feature of the herbicide composition of the present invention is that a high herbicidal effect on many weeds can be obtained by combining low dosages that could not be expected from the herbicidal effect of each active ingredient alone. I can list things that I can do.

また本発明の除草剤組成物は、生育初期段階の雑草のみ
ならず、ある程度生育の進んだ段階の雑草に対しても顕
著な除草活性を示すため、田植前後の雑草の発芽始期か
ら雑草の生育期にわたり、処理適期幅の広いことも優れ
た特徴の一つである。
In addition, the herbicide composition of the present invention exhibits remarkable herbicidal activity not only against weeds at the early stage of growth but also against weeds at a certain stage of advanced growth. One of its excellent features is that it has a wide range of suitable processing periods.

さらに防除しうる雑草の種類も極めて多く、ノビエ、タ
マガヤツリ、コナギ、キカシグサ等の一年生雑草をはじ
め、ホタルイ、ミズガヤツリ、ウリカワ等の多年生雑草
に対しても著しい除草効果が認められる。しかも移植水
稲に対しては薬害を生じることがなく、安全性の高い高
度選択性除草剤として利用価値の高いものである。その
上各有効成分の残効性が長いため、長期間にわたつて高
い除草活性を示し、多くの雑草を防除することができ、
散布労力の節減、すなわち農作業の省力化に貢献すると
ころは大きい。
In addition, there are many types of weeds that can be controlled, and a remarkable herbicidal effect has been observed on annual weeds such as Japanese wild grass, Japanese cypress, Japanese cypress, and perennial weeds such as Japanese firefly, Japanese cypress, and Japanese snail. Moreover, it does not cause any chemical damage to transplanted paddy rice, making it highly useful as a highly safe and highly selective herbicide. Furthermore, each active ingredient has a long residual effect, so it exhibits high herbicidal activity over a long period of time and can control many weeds.
It greatly contributes to the reduction of spraying labor, that is, the labor saving of agricultural work.

以上のごとく、本発明の除草剤組成物は多くの優れた特
徴を有しており、実用性の大きいものである。
As described above, the herbicidal composition of the present invention has many excellent features and is highly practical.

Claims (1)

【特許請求の範囲】[Claims] O−3−tert−ブチルフェニルN−(6−メトキシ
−2−ピリジル)−N−メチルチオカーバメートまたは
O−4−tert−ブチルフェニルN−(6−メトキシ
−2−ピリジル)−N−メチルチオカーバメートの1種
または2種と、N−(α,α−ジメチルベンジル)−2
−ブロモ−3,3−ジメチルブチルアミドおよび4−(
2,4−ジクロロベンゾイル)−1,3−ジメチル−5
−フェナシルオキシピラゾールとを有効成分とする除草
剤組成物。
O-3-tert-butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate or O-4-tert-butylphenyl N-(6-methoxy-2-pyridyl)-N-methylthiocarbamate 1 type or 2 types and N-(α,α-dimethylbenzyl)-2
-bromo-3,3-dimethylbutyramide and 4-(
2,4-dichlorobenzoyl)-1,3-dimethyl-5
- A herbicide composition containing phenacyloxypyrazole as an active ingredient.
JP62032385A 1987-02-17 1987-02-17 Herbicide composition Pending JPS63201104A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62032385A JPS63201104A (en) 1987-02-17 1987-02-17 Herbicide composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62032385A JPS63201104A (en) 1987-02-17 1987-02-17 Herbicide composition

Publications (1)

Publication Number Publication Date
JPS63201104A true JPS63201104A (en) 1988-08-19

Family

ID=12357488

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62032385A Pending JPS63201104A (en) 1987-02-17 1987-02-17 Herbicide composition

Country Status (1)

Country Link
JP (1) JPS63201104A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008155027A3 (en) * 2007-06-19 2009-10-22 Bayer Cropscience Ag Synergistic crop-tolerated combinations of herbicides from the benzoylcyclohexandione group for application in rice growing

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2008155027A3 (en) * 2007-06-19 2009-10-22 Bayer Cropscience Ag Synergistic crop-tolerated combinations of herbicides from the benzoylcyclohexandione group for application in rice growing
US8673814B2 (en) 2007-06-19 2014-03-18 Bayer Cropscience Ag Synergistic combinations which are compatible with cultivated plants and which comprise herbicides selected from the group consisting of benzoylcyclohexanediones for use in rice crops

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