JPH0331204A - Herbicide composition for paddy field - Google Patents

Herbicide composition for paddy field

Info

Publication number
JPH0331204A
JPH0331204A JP16606889A JP16606889A JPH0331204A JP H0331204 A JPH0331204 A JP H0331204A JP 16606889 A JP16606889 A JP 16606889A JP 16606889 A JP16606889 A JP 16606889A JP H0331204 A JPH0331204 A JP H0331204A
Authority
JP
Japan
Prior art keywords
group
lower alkyl
compound
alpha
herbicide composition
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
JP16606889A
Other languages
Japanese (ja)
Inventor
Yasuo Morishima
森島 靖雄
Hirokazu Osabe
長部 広和
Yukihisa Goto
幸久 後藤
Takeshi Hamaya
武 濱谷
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.)
Daicel Corp
Japan Carlit Co Ltd
Original Assignee
Japan Carlit Co Ltd
Daicel Chemical Industries 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 Japan Carlit Co Ltd, Daicel Chemical Industries Ltd filed Critical Japan Carlit Co Ltd
Priority to JP16606889A priority Critical patent/JPH0331204A/en
Publication of JPH0331204A publication Critical patent/JPH0331204A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain the title compound effective and safe to a wide range of weeds in a growth period with a small amount of herbicide, comprising a pyrone-3-carboxamide derivative and 1(2-chlorobenzyl)-3-(alpha,alpha-dimethylbenzyl)urea as active ingredients. CONSTITUTION:A herbicide composition for paddy field comprising at least one pyrone-3-carboxamide derivative shown by the formula [R1 and R3 are the same or different lower alkyl, lower alkenyl or lower alkynyl; R2 is H, halogen, lower alkyl, lower alkoxy or H2 and R3 are bonded to form -(CH2)m- (m is 3 or 4); X is halogen, cyano, nitro, amino, lower alkyl or halogenated lower alkyl] and 1-(2-chlorobenzyl)-3-(alpha,alpha-dimethylbenzyl)urea as active ingredients. The blending ratio is the ratio of the former: the latter of 1:(0.5-30), preferably 1:(1-20) by weight.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は新規な水田用除草剤組成物に関するものである
DETAILED DESCRIPTION OF THE INVENTION [Industrial Field of Application] The present invention relates to a novel herbicide composition for paddy fields.

〔従来の技術及びその課題〕[Conventional technology and its problems]

現在、農業用に多種類の除草剤が上市されており、広く
一般に使用されている。しかしながら農耕地における雑
草は非常に多種多様に及んでおり、単独の除草剤で広範
な殺草スペクトラムを有し、かつ薬害の全くないという
条件を満足するものは皆無といえる。そのため、各々の
欠点を補う意味で2種以上の除草剤を混合して使用する
方法が行われており、特に水田用除草剤としての混合剤
は多種に及んでいる。
Currently, many types of herbicides for agricultural use are on the market and are widely used. However, there are a wide variety of weeds in agricultural land, and it can be said that there is no single herbicide that satisfies the requirements of having a broad herbicidal spectrum and being completely free from chemical damage. Therefore, a method of using a mixture of two or more herbicides has been carried out in order to compensate for the drawbacks of each herbicide, and in particular, there are many types of herbicides used as herbicides for paddy fields.

しかしながら、最近の水稲栽培は機械化の導人、移植時
期の早期化が急速に広まり、又労働力不足による整備不
良水田の増加等により、従来以上に雑草発生に好適な条
件を与えている。
However, in recent years, rice cultivation has become more mechanized, the transplanting period has been rapidly advanced, and the number of poorly maintained paddy fields due to labor shortages has increased, creating conditions more suitable for weeds to grow than ever before.

従って、単剤では当然のこと、上述したような混合剤に
おいても同一の水田で数回にわたって繰り返し使用しな
いと満足な除草効果が期待できなくなってきているが、
このような除草剤の使用状態は、多大の労力を必要とす
るばかりか、多量使用による薬害の発生や、環境汚染等
の原因となる。
Therefore, it is no longer possible to expect a satisfactory herbicidal effect when using a single agent, or even when using a mixture as described above, unless it is repeatedly used several times in the same paddy field.
The use of such herbicides not only requires a great deal of labor, but also causes chemical damage and environmental pollution due to the use of large amounts.

〔課題を解決するための手段) 本発明は従来の除草剤の上記の如き問題点に鑑みなされ
たものであり、本発明者らは一回の施用で全雑草種を完
全に駆除し、しかも薬害が極めて小さくかつ人畜毒性の
低い除草剤の探索を続けた結果、異なった除草作用を有
する2種類の除草剤を配合、併用することにより上記問
題点を改良できることを見出し本発明を完成するに至っ
た。
[Means for Solving the Problems] The present invention was made in view of the above-mentioned problems of conventional herbicides, and the present inventors have achieved a method that completely exterminates all weed species with a single application. As a result of continuing to search for herbicides that cause extremely little chemical damage and low toxicity to humans and animals, we discovered that the above problems could be improved by blending and using two types of herbicides with different herbicidal actions in combination, and completed the present invention. It's arrived.

すなわち本発明は、下記一般式+I+ 〔式中、R2とR1は同−又は異なって低級アルキル基
、低級アルケニル基、又は低級アルキニル基を、R3は
水素原子、ハロゲン原子、低級アルキル基、又は低級ア
ルコキシ基を表し、あるいはR2とR3は一緒に−(C
)IZ)、−(mは3又は4)を表し、χはハロゲン原
子、シアノ基、ニトロ基、アミノ基、低級アルキル基、
ハロゲン化低級アルキル基、ヒドロキシ基、低級アルコ
キシ基、アリールオキシ基、カルホキシル基、又は低級
アルコキシカルボニル基を意味する。] で表されるピロン−3−カルボキサミド誘導体(以下、
化合物Aという)の少なくとも1種と、1−(2−クロ
ロベンジル)−3−(α、α−ジメチルベンジル)ウレ
ア(以下、化合物Bという)とを有効成分として含有す
ることを特徴とする水田用除草剤組成物を提供するもの
である。
That is, the present invention provides the following general formula represents an alkoxy group, or R2 and R3 together represent -(C
)IZ), -(m is 3 or 4), χ is a halogen atom, a cyano group, a nitro group, an amino group, a lower alkyl group,
It means a halogenated lower alkyl group, hydroxy group, lower alkoxy group, aryloxy group, carboxyl group, or lower alkoxycarbonyl group. ] Pyrone-3-carboxamide derivative (hereinafter referred to as
A rice field characterized by containing at least one type of compound A) and 1-(2-chlorobenzyl)-3-(α,α-dimethylbenzyl)urea (hereinafter referred to as compound B) as active ingredients. The present invention provides a herbicide composition for use in pesticides.

本発明の除草剤組成物の有効成分のうち、化合物Aは、
特開昭63−115878号公報に記載された公知の化
合物であり、水田のタイヌビエ等のイネ科雑草から、カ
ヤツリグサ科雑草及び広葉雑草にかけての広範なスペク
トラムを有しているが、単独使用では生育の進んだホタ
ルイ、ミズガヤツリ等の多年生雑草に効果が低いという
欠点を有する。
Among the active ingredients of the herbicide composition of the present invention, compound A is
It is a well-known compound described in Japanese Patent Application Laid-Open No. 63-115878, and has a wide spectrum from grass weeds such as Japanese millet in rice fields to Cyperaceae weeds and broad-leaved weeds, but it does not grow well when used alone. It has the disadvantage that it is less effective against perennial weeds such as advanced firefly and cypress.

一方化合物Bは、特開昭60−172910号公報に記
載された公知の化合物であり、水田のホタルイ、マツバ
イをはじめとするカヤツリグサ科雑草に効果が高いが、
単独使用では広葉雑草や生育の進んだタイヌビエ等のイ
ネ科雑草には効果を期待できないという欠点を有する。
On the other hand, compound B is a known compound described in JP-A-60-172910, and is highly effective against weeds of the Cyperaceae family, including firefly and pineweed in rice fields.
When used alone, it has the disadvantage that it cannot be expected to be effective against broad-leaved weeds or weeds of the grass family, such as grass millet, which have advanced growth.

本発明者らはそれぞれ前記のような欠点を有する化合物
Aと化合物Bとを適当な割合で混合使用することにより
、それぞれ単独使用での欠点を補い、著しい相乗効果に
より殺草スペクトラムが拡大され、−年生雑草から多年
生雑草の生育初期から生育期にかけて少量の薬量で、し
かも−回散布により水稲の全生育期間にわたって高い除
草効果が持続し、かつ薬害がない等の優れた効果が得ら
れるという事実を見出した。
By using Compound A and Compound B, each of which has the above-mentioned drawbacks, in a mixture in an appropriate ratio, the present inventors compensate for the drawbacks of using each alone, and the herbicidal spectrum is expanded due to a significant synergistic effect. - By applying a small amount of the chemical from the early stage of growth to the growing season of annual to perennial weeds, and by spraying it multiple times, a high herbicidal effect can be maintained throughout the entire growing period of paddy rice, and excellent effects such as no chemical damage can be obtained. I found out the truth.

すなわち化合物Aと化合物B2:を適当な割合で混合使
用するとタイヌビエや各種の広葉雑草に相乗的効果を発
揮し、又ミズガヤツリやホタルイ等のカヤツリグサ科雑
草に対する効果の安定も期待でき、かつ水稲に対する安
全性は損なわれず、問題となような薬害は生じない。
In other words, when Compound A and Compound B2 are mixed and used in an appropriate ratio, it can be expected to have a synergistic effect on Japanese millet and various broad-leaved weeds, and also be expected to have a stable effect on Cyperaceae weeds such as Cyperus and Cyperus, and is safe for paddy rice. Its properties are not impaired, and no problematic chemical damage occurs.

ピロン−3−カルボキサミドに属する化合物で、除草活
性を有するものについては前述した特開昭63−115
878号公報等で知られているが、本発明に示された水
田用除草剤組成物は文献未記載の新規な組み合わせであ
り、もちろんその特異な除草効果について言及した文献
もない。
Compounds belonging to pyrone-3-carboxamide and having herbicidal activity are disclosed in the above-mentioned Japanese Patent Application Laid-open No. 63-115.
Although it is known from Publication No. 878 and the like, the herbicidal composition for rice fields shown in the present invention is a novel combination that has not been described in any literature, and of course there is no literature that mentions its unique herbicidal effect.

化合物への例を表−1に示す。(以下、化合物Aの例示
は表−1中の化合物Nαで示す。)本発明の水田用除草
剤組成物の特異な除草効果は、化合物Aと化合物Bとを
相当広範囲の割合で配合しても認められるが、好ましく
はA:8重量比で1:0.5〜30、より好ましくは1
:1〜20の範囲である。
Examples of compounds are shown in Table-1. (Hereinafter, an example of Compound A is shown as Compound Nα in Table 1.) The unique herbicidal effect of the herbicide composition for rice fields of the present invention is due to the fact that Compound A and Compound B are blended in a fairly wide range of ratios. Although A:8 weight ratio is preferably 1:0.5 to 30, more preferably 1:
: range of 1 to 20.

本発明の除草剤組成物はそのまま使用してもよいが、一
般には固体担体、液体担体、界面活性剤、その他の製剤
用補助剤と混合して、乳剤、水和剤、懸濁製剤等に製剤
して用いる。
Although the herbicidal composition of the present invention may be used as is, it is generally mixed with a solid carrier, liquid carrier, surfactant, or other formulation auxiliary to form an emulsion, wettable powder, suspension formulation, etc. Prepare and use.

これらの製剤には本発明の除草剤組成物を化合物A及び
化合物Bの有効成分の合計として水和剤や懸濁剤では1
0〜80%、粒剤では2〜10%、乳剤では10〜50
%(いずれも重量%)含有することが好ましい。
In these preparations, the herbicide composition of the present invention is added to the total amount of active ingredients of Compound A and Compound B in wettable powders or suspensions.
0-80%, 2-10% for granules, 10-50 for emulsions
% (all % by weight).

製剤化に際して使用される固体担体には、カオリン、ベ
ントナイト、クレー類、タルク、珪藻土、ジ−クライト
、ゼオライト、パイロフィライト、合成含酸化珪素、炭
酸カルシウム等の微粉末あるいは粒状物等があり、また
液体担体にはキシレン、メチルナフタレン等の芳香族炭
化水素類、エタノール、イソプロパツール、エチレング
リコール、メチルセロソルブ等のアルコール類、アセト
ン、イソホロン、シクロヘキサノン等のケトン類、大豆
油、綿実油等の植物油、ジメチルホルムアミド、ジメチ
ルスルホキシド、アセトニトリル、水等がある。
Solid carriers used in formulation include fine powders or granules of kaolin, bentonite, clays, talc, diatomaceous earth, gicrite, zeolite, pyrophyllite, synthetic silicon oxide, calcium carbonate, etc. Liquid carriers include aromatic hydrocarbons such as xylene and methylnaphthalene, alcohols such as ethanol, isopropanol, ethylene glycol, and methyl cellosolve, ketones such as acetone, isophorone, and cyclohexanone, and vegetable oils such as soybean oil and cottonseed oil. , dimethylformamide, dimethylsulfoxide, acetonitrile, water, etc.

また、分散、乳化等のために用いられる界面活性剤とし
ては、ポリオキシエチレンアルキルエーテル、ポリオキ
シエチレンアルキルアリールエーテル、ポリオキシエチ
レン脂肪酸エステル、ソルビタン脂肪酸エステル、ポリ
オキシエチレンポリオキシブロピレンプロックボリマー
等のノニオン性界面活性剤、アルキル硫酸エステル塩、
アルキルスルホン酸塩、アルキルアリールスルホン酸塩
、ポリオキシエチレンアルキル硫酸エステル塩等のアニ
オン性界面活性剤等が挙げられる。
In addition, surfactants used for dispersion, emulsification, etc. include polyoxyethylene alkyl ether, polyoxyethylene alkylaryl ether, polyoxyethylene fatty acid ester, sorbitan fatty acid ester, polyoxyethylene polyoxypropylene block polymer. nonionic surfactants such as, alkyl sulfate ester salts,
Examples include anionic surfactants such as alkyl sulfonates, alkylaryl sulfonates, and polyoxyethylene alkyl sulfate salts.

製剤用補助剤には、リグニンスルホン酸塩、アルギン酸
塩、ポリアクリレート類、ポリビニルアルコール、植物
ガム類、カルボキシメチルセルロース(CMC) 、ヒ
ドロキシエチルセルロース(HEC)等がある。
Formulation adjuvants include lignin sulfonates, alginates, polyacrylates, polyvinyl alcohol, vegetable gums, carboxymethyl cellulose (CMC), hydroxyethyl cellulose (HEC), and the like.

次に本発明の除草剤組成物を用いた製剤例を示すが、本
発明はこれらに限定されるものではない、尚、部は重量
部を示す。
Next, formulation examples using the herbicide composition of the present invention will be shown, but the present invention is not limited thereto. Note that parts indicate parts by weight.

製剤例1・・・水和剤 化合物A−95部 化合物8          20部 タルク            50部ベントナイト 
       20部 ツルポール5039 (東邦化学型) 3部 く粉砕混合して水和剤を得る。
Formulation example 1... Wettable powder Compound A-95 parts Compound 8 20 parts Talc 50 parts Bentonite
20 parts Tsurupol 5039 (Toho Kagaku type) 3 parts are ground and mixed to obtain a wettable powder.

上記の成分をよ 製剤例2・・・粒 剤 化合物A−6 化合物B タルク ベントナイト リグニンスルホン酸塩 0、5部 5部 60部 31.5部 3部 上記の成分をよく粉砕混合し、水を加えてよく練り合わ
せ、通常の方法によって造粒して粒剤を得る。
Formulation Example 2 Granules Compound A-6 Compound B Talcum bentonite lignin sulfonate 0.5 parts 5 parts 60 parts 31.5 parts 3 parts The above ingredients were thoroughly ground and mixed, and water was added. The mixture is added, kneaded well, and granulated by a conventional method to obtain granules.

製剤例3・・・懸濁製剤 化合物A−166部 化合物8          30部 エチレングリコール      2部 ニエーカルゲンCP−15−200  5部(竹本油脂
製) ニューカルゲンPS−P3部 (竹本油脂製) プロナール502       0.5部(東邦化学型
) キサンタンガム     55.5部 0.15%水溶液 上記の成分をよく混合し、粒度が5ミクロン以下になる
まで湿式粉砕して懸濁製剤を得る。
Formulation example 3 Suspension formulation Compound A-166 parts Compound 8 30 parts Ethylene glycol 2 parts Niercalgen CP-15-200 5 parts (Takemoto Yushi) 3 parts Nucalgen PS-P (Takemoto Yushi) Pronal 502 0. 5 parts (Toho Chemical Type) Xanthan gum 55.5 parts 0.15% aqueous solution The above ingredients are mixed well and wet-pulverized until the particle size is 5 microns or less to obtain a suspension preparation.

以上のようにして製剤された本発明の水田用除草剤組成
物は、水和剤は通常水で希釈して、粒剤、懸濁製剤はそ
のままで土壌散布あるいは茎葉兼土壌散布して使用する
In the herbicide composition for paddy fields of the present invention formulated as described above, the wettable powder is usually diluted with water, and the granule and suspension formulations are used as they are by spraying on the soil or on the foliage and on the soil. .

また、上記製剤の施用量は、化合物A、Bの混合比、製
剤形態、対象雑草の種類、生育状況、気象条件等により
異なるが、通常1アール当たり化合物A及び化合物Bの
有効成分の合計量で1g〜80g、好ましくは2g〜s
ogである。
In addition, the application amount of the above preparation varies depending on the mixing ratio of Compounds A and B, the formulation form, the type of target weed, growth conditions, weather conditions, etc., but usually the total amount of the active ingredients of Compound A and Compound B per 1 are. 1g to 80g, preferably 2g to s
It is og.

更に本発明の水田用除草剤組成物は、必要に応じて他の
殺虫剤、殺ダニ剤、殺線虫剤、殺菌剤、除草剤、植物成
長調節剤等と混合して使用することもできる。
Furthermore, the herbicide composition for rice fields of the present invention can be used in combination with other insecticides, acaricides, nematicides, fungicides, herbicides, plant growth regulators, etc., as necessary. .

〔実施例〕〔Example〕

次に、本発明の有用性を実施例にて説明するが、本発明
はこれらの実施例に限定されるものではない。
Next, the usefulness of the present invention will be explained using Examples, but the present invention is not limited to these Examples.

実施例1 115000aのワグナ−ポンドに水田土壌を詰め、タ
イヌビエ、コナギ、クマガヤツリ、ホタルイ、広葉雑草
(アゼナ、キカシグサ、ミゾハコベ)の各種子及びマツ
バイ塊茎を1〜2cmの深さに混入した。湛水化かきし
て水田状態とした後、ミズガヤツリ塊茎を植え込み、3
.2葉期の水稲を2株(2本/株)ずつ移植した。尚、
温水深さは3C1とした。
Example 1 A 115,000-a Wagner pond was filled with paddy soil, and seeds of Japanese millet, Japanese grasshopper, Japanese cypress, firefly, and broad-leaved weeds (Azaena, Japanese sagebrush, and Japanese chickweed) and Pinus cabbage tubers were mixed in at a depth of 1 to 2 cm. After flooding and making it into a paddy field, we planted the tubers of Mizugaya spp.
.. Two plants (2 plants/plant) of paddy rice at the two-leaf stage were transplanted. still,
The warm water depth was set to 3C1.

水稲移植の2日後(雑草発生始期)及び約6日後(タイ
ヌビエ1葉期)に、製剤例1に準じて、化合物A及び化
合物Bを表−3及び表−4に示すように配合して水和剤
とした薬剤の所定量を湛水面に滴下処理した。
Two days after transplanting paddy rice (weed initiation stage) and about 6 days after transplantation (first leaf stage of Japanese millet), Compound A and Compound B were mixed as shown in Tables 3 and 4 according to Formulation Example 1, and water was added. A predetermined amount of the chemical compound was dropped onto the flooded surface.

それぞれ薬剤処理の30日後に除草効果及び薬害につい
ての評価を表−2に示す判定基準に従って行った。
Thirty days after each chemical treatment, herbicidal effects and chemical damage were evaluated according to the criteria shown in Table 2.

表−2 雑草発生始期の評価結果を表−3に、タイヌビエ1葉期
の評価結果を表−4に示す。
Table 2 The evaluation results for the initial stage of weed emergence are shown in Table 3, and the evaluation results for the first leaf stage of Japanese millet are shown in Table 4.

Claims (1)

【特許請求の範囲】 1 下記一般式( I ) ▲数式、化学式、表等があります▼( I ) 〔式中、R_1とR_3は同一又は異なって低級アルキ
ル基、低級アルケニル基、又は低級アルキニル基を、R
_2は水素原子、ハロゲン原子、低級アルキル基、又は
低級アルコキシ基を表し、あるいはR_2とR_3は一
緒に−(CH_2)_m−(mは3又は4)を表し、X
はハロゲン原子、シアノ基、ニトロ基、アミノ基、低級
アルキル基、ハロゲン化低級アルキル基、ヒドロキシ基
、低級アルコキシ基、アリールオキシ基、カルボキシル
基、又は低級アルコキシカルボニル基を意味する。〕 で表されるピロン−3−カルボキサミド誘導体の少なく
とも1種と、1−(2−クロロベンジル)−3−(α,
α−ジメチルベンジル)ウレアとを有効成分として含有
することを特徴とする水田用除草剤組成物。
[Claims] 1 The following general formula (I) ▲There are mathematical formulas, chemical formulas, tables, etc.▼ (I) [In the formula, R_1 and R_3 are the same or different and are a lower alkyl group, a lower alkenyl group, or a lower alkynyl group , R
_2 represents a hydrogen atom, a halogen atom, a lower alkyl group, or a lower alkoxy group, or R_2 and R_3 together represent -(CH_2)_m- (m is 3 or 4), and
means a halogen atom, cyano group, nitro group, amino group, lower alkyl group, halogenated lower alkyl group, hydroxy group, lower alkoxy group, aryloxy group, carboxyl group, or lower alkoxycarbonyl group. ] At least one pyrone-3-carboxamide derivative represented by and 1-(2-chlorobenzyl)-3-(α,
1. A herbicide composition for paddy fields, characterized by containing α-dimethylbenzyl)urea as an active ingredient.
JP16606889A 1989-06-28 1989-06-28 Herbicide composition for paddy field Pending JPH0331204A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP16606889A JPH0331204A (en) 1989-06-28 1989-06-28 Herbicide composition for paddy field

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP16606889A JPH0331204A (en) 1989-06-28 1989-06-28 Herbicide composition for paddy field

Publications (1)

Publication Number Publication Date
JPH0331204A true JPH0331204A (en) 1991-02-12

Family

ID=15824382

Family Applications (1)

Application Number Title Priority Date Filing Date
JP16606889A Pending JPH0331204A (en) 1989-06-28 1989-06-28 Herbicide composition for paddy field

Country Status (1)

Country Link
JP (1) JPH0331204A (en)

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