JPS5827765B2 - Tansuiden Youjiyosouzai - Google Patents

Tansuiden Youjiyosouzai

Info

Publication number
JPS5827765B2
JPS5827765B2 JP15281175A JP15281175A JPS5827765B2 JP S5827765 B2 JPS5827765 B2 JP S5827765B2 JP 15281175 A JP15281175 A JP 15281175A JP 15281175 A JP15281175 A JP 15281175A JP S5827765 B2 JPS5827765 B2 JP S5827765B2
Authority
JP
Japan
Prior art keywords
parts
rice
paddy
agent
water
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
JP15281175A
Other languages
Japanese (ja)
Other versions
JPS5276431A (en
Inventor
真 永富
誠登 近内
隆之 五十川
哲夫 竹松
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.)
Hodogaya Chemical Co Ltd
Original Assignee
Hodogaya Chemical 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 Hodogaya Chemical Co Ltd filed Critical Hodogaya Chemical Co Ltd
Priority to JP15281175A priority Critical patent/JPS5827765B2/en
Publication of JPS5276431A publication Critical patent/JPS5276431A/en
Publication of JPS5827765B2 publication Critical patent/JPS5827765B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Agricultural Chemicals And Associated Chemicals (AREA)

Description

【発明の詳細な説明】 本発明は、3・4−ジクロルプロピオンアニリド(以下
DCPAという)、特定のカーバメート化合物および特
定の酸アミド化合物を有効成分として含有する湛水田用
除草剤に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a herbicide for flooded fields containing 3,4-dichloropropionanilide (hereinafter referred to as DCPA), a specific carbamate compound, and a specific acid amide compound as active ingredients. .

DCPAは、茎葉処理剤としてイネに薬害なく、稲作の
主要雑草であるノビエを防除しうるとともに、幼少期の
広葉雑草を防除しうるため、広く稲作用除草剤として用
いられている。
DCPA is widely used as a herbicide for rice cultivation as a foliage treatment agent that does not cause any chemical damage to rice, and can control the major weeds of rice cultivation, Novieum, as well as young broad-leaved weeds.

しかしながら、この薬剤は水が存在すると著しく活性が
減殺し、土壌表面が湿っている場合には著しく効果が低
下する。
However, the activity of this agent is significantly reduced in the presence of water, and its effectiveness is significantly reduced when the soil surface is moist.

さらに湛水下では、はとんど雑草防除効果を発揮するこ
とができない。
Furthermore, under waterlogged conditions, it is difficult to exert any weed control effect.

このため、この薬剤を用いるには、あらかじめ水田を落
水して処理し、処理後2〜3日間は、降雨をさけねばな
らず、処理時期の制約のほか、落水、入水という余分の
労力を必要とする。
Therefore, in order to use this chemical, it is necessary to first treat rice fields by dropping them into water, and then avoid rain for 2 to 3 days after treatment, which not only limits the timing of the treatment, but also requires extra labor for dropping and soaking into the water. shall be.

このようなりCPAの問題点を解決するため、本発明者
は種々研究した結果、特定のカーバメーI・化合物およ
び特定の酸アミド化合物の特異な作用を見出し、本発明
を完成させた。
In order to solve these problems of CPA, the present inventor conducted various researches, discovered the unique effects of a specific carbame I compound and a specific acid amide compound, and completed the present invention.

本発明は、DCPA、β−ナフチル−N−メチルカーバ
メート(以下 β−NACという)および2−クロル−
2/・6−シエチルーN(ブトキシメチル)−アセトア
ニリド(以下 ブタクロールという)を含有することを
特徴とする湛水田用除草剤である。
The present invention relates to DCPA, β-naphthyl-N-methylcarbamate (hereinafter referred to as β-NAC) and 2-chloro-
This herbicide for flooded rice fields is characterized by containing 2/.6-ethyl-N(butoxymethyl)-acetanilide (hereinafter referred to as butachlor).

本発明の除草剤を使用するには、 10アール当り、 PCPAを50〜500P、好ましくは100〜400
グ、さらに好ましくは150〜4oO2、β−NACを
2〜30グ、好ましくは5〜20グ、さらに好ましくは
5〜151、ブタクロールを25〜4001、好ましく
は50〜30o1、さらに好ましくは50〜20010
割合で混合使用する。
To use the herbicide of the present invention, 50 to 500 PCPA, preferably 100 to 400 PCPA per 10 are.
g, more preferably 150-4oO2, β-NAC 2-30g, preferably 5-20g, even more preferably 5-151, butachlor 25-4001, preferably 50-30o1, even more preferably 50-20010
Mix and use in proportion.

本発明剤は、使用場面に応じて、乳剤、水相剤、粒剤な
ど適宜の剤形な選ぶことができる。
The agent of the present invention can be in an appropriate dosage form, such as an emulsion, an aqueous phase, or a granule, depending on the situation of use.

製剤に当たっては、目的とする剤形に応じて、前記の各
成分に不活性担体を用いて、農薬の一般的製剤手段によ
って製剤することができる。
The formulation can be prepared by adding an inert carrier to each of the above-mentioned components, depending on the intended dosage form, and using common methods for formulating agricultural chemicals.

DCPAは植物の茎葉に散布しなげれば効果を発揮でき
ないとされている。
DCPA is said to be ineffective unless it is sprayed on the leaves and stems of plants.

本発明剤は、DCPA単剤では不可能な、湛水中の田水
中に処理することによっても除草活性を発揮させ得るの
である。
The agent of the present invention can exhibit herbicidal activity even when applied to flooded field water, which is not possible with DCPA alone.

DCPAとβ−NACとの湿剤にさらにブタクロールを
混用することにより、一層少い薬量で、速かに広い範囲
の草種を抑制でき、しかも、その抑制効果を一層持続さ
せることができる。
By further adding butachlor to the wetting agent of DCPA and β-NAC, a wide range of grass species can be quickly controlled with a smaller dosage, and the suppressive effect can be further sustained.

以下に実施例によって本発明を説明する。The present invention will be explained below by way of examples.

実施例 1 乳剤 DCPA20部(部は重量部、以下同じ)、βNAC1
部、ブタクロール10部、キシレン30部、シクロヘキ
サノン29部およびツルポール(東邦化学工業■商標)
800A、10部を混合溶解して乳剤を調製した。
Example 1 Emulsion DCPA 20 parts (parts are parts by weight, the same applies hereinafter), βNAC 1
part, butachlor 10 parts, xylene 30 parts, cyclohexanone 29 parts and Tulpol (Toho Chemical Industry Trademark)
An emulsion was prepared by mixing and dissolving 10 parts of 800A.

実施例 2 水相剤 DCPA30部、β−NACI部、ブタクロール15部
、ホワイトカーボン5部、カオリンクレー44部および
ツルポール5039.5部を混合し、均一に攪拌して水
相剤を調製した。
Example 2 Water phase agent 30 parts of DCPA, part β-NACI, 15 parts of butachlor, 5 parts of white carbon, 44 parts of kaolin clay, and 5039.5 parts of Tsurpol were mixed and uniformly stirred to prepare a water phase agent.

実施例 3 粒剤 DCPA9部、β−NAC0,3部、ブタクロール4部
、カオリンクレーとベントナイトとの等景況合物81.
3部およびリグニンスルホン酸カルシ**ウム5部を混
合攪拌し、少量の水を加えて紳り、造粒機を用いて粒状
としたのち乾燥して粒剤を調製した。
Example 3 Granules: 9 parts of DCPA, 0.3 parts of β-NAC, 4 parts of butachlor, isostatic compound of kaolin clay and bentonite 81.
3 parts and 5 parts of calci**ium lignosulfonate were mixed and stirred, mixed with a small amount of water, made into granules using a granulator, and dried to prepare granules.

以下に試、部側によって本発明の詳細な説明する。The present invention will be described in detail below by reference.

試1験例 1 稚苗移植栽培 5千分の1アールのワグネルポットに水田土壌をつめ、
ノビエ種子および各種水1ヨ雑草種子を含む水田土壌を
表層に加え、代かきを行なった後、3葉の水稲苗(品種
:コシヒカリ)を1株2本植で3株移植し、3〜4cr
rLの湛水状態で育成管理した、ノビエが発芽し3〜3
.5葉期に達した時、湛水4CrrLで、実施例1の乳
剤の水による希釈液の所定量を、植物体の茎葉に耐着し
ないよう、ピペットで滴下処理した。
Test 1 Example 1 Transplant cultivation of young seedlings Fill a Wagner pot with a size of 1/5000 are and fill it with paddy soil.
Paddy soil containing wildflower seeds and various weed seeds was added to the surface layer, and after plowing, three 3-leaf rice seedlings (variety: Koshihikari) were transplanted with 2 plants each to produce 3 to 4 cr.
Novies grown and managed under flooded conditions of rL germinated and reached 3-3
.. When the plant reached the 5-leaf stage, a predetermined amount of the diluted solution of the emulsion of Example 1 with water was dripped with a pipette at 4 CrrL of water so as not to adhere to the stems and leaves of the plant.

その後、試験期間中は湛水4αで繰過させた。Thereafter, the water was repeated at 4α during the test period.

処理後20日目に、各雑草に対する効果および水稲の損
傷程度を観察し、その結果を第1表に示す。
On the 20th day after the treatment, the effects on each weed and the degree of damage to the paddy rice were observed, and the results are shown in Table 1.

なお、表中の評価は下記の基準により行った。In addition, the evaluation in the table was performed based on the following criteria.

10完全枯死〜0無害 第1表により明らかなとおり、対照区の各単剤では水田
湛水生育期処理において実用的効果をもたない。
10 Complete withering to 0 Harmless As is clear from Table 1, each single agent in the control plot has no practical effect in the treatment during the growing season of flooded paddy fields.

しかるに、本発明によれば、活性は著しく高まり低薬量
で全草種をほぼ完全に枯殺し、しかも水稲に対する薬害
はみられない。
However, according to the present invention, the activity is significantly increased and all plant species are almost completely killed with a low dose, and no chemical damage to paddy rice is observed.

試験例 2 湛水直播栽培 5千分の1アールのワグネルポットに水田土壌をつめ、
表層3CrrLに各種水田雑草種子を含む水田土壌を加
えて代かきした後、イネの鳩胸状の催芽**種子を1ポ
ット当り30粒播種1(品種:コシヒカリ)、湛水1〜
2cmにて育成管理した。
Test example 2 Filled with paddy soil in a Wagner pot of 1/5000 are for direct sowing cultivation.
After adding paddy soil containing seeds of various paddy weeds to the surface layer 3CrrL and plowing it, sow 30 pigeon-breasted germinated seeds of rice per pot 1 (variety: Koshihikari), submerged 1~
Growth was controlled at 2 cm.

ノビエが3.5〜4葉期、イネが3〜3.5葉期に達し
た時、湛水3(Jで、実施例2の水相剤の水による希釈
液を所定量、植物の芽葉に接触しないようピペットで滴
下処理した。
When the wildflowers reached the 3.5-4 leaf stage and the rice reached the 3-3.5 leaf stage, a predetermined amount of the aqueous phase agent of Example 2 diluted with water was added to the buds of the plants. It was applied dropwise with a pipette so as not to touch the leaves.

処理後25日目に試1験例1と同様の評価基準に従って
観察調査した。
On the 25th day after the treatment, observation and investigation were conducted according to the same evaluation criteria as in Test Example 1.

比較のため、単剤についても同様試験を行った。For comparison, a similar test was also conducted for a single drug.

その結果を第2表に示す。The results are shown in Table 2.

第2表に示すとおり、各単剤の処理では、高処理量にお
いても、ノビエをはじめとした水田雑草にほとんど活性
を示さない。
As shown in Table 2, each single agent treatment shows almost no activity against paddy field weeds, including field weeds, even at high treatment rates.

これに対して、本発明によれば低薬量で所望の除草効果
を挙げ、しかも速やかに完全に雑草を抑制枯殺できる。
In contrast, according to the present invention, the desired herbicidal effect can be achieved with a low dose, and weeds can be quickly and completely suppressed and killed.

これに加えてイネには全く薬害がみられない。In addition to this, no chemical damage is observed in rice.

試1験例 3 2千分の1アールのワグネルボットに水田土壌をつめ、
表層にノビエを始めとした各種水田雑草種子を含む水田
土壌を加え、入水し、代かきしだ後25〜3葉期の水稲
苗(品種二日本晴)を1株*木2本植で3株移植し、湛
水3〜4cTLで育成管理した。
Test 1 Test Example 3 Pack paddy soil into a 1/2,000 are Wagnerbot,
Add paddy soil containing seeds of various paddy field weeds, including grasshoppers, to the surface layer, and transplant 3 paddy rice seedlings (cultivar Ni Nihonbare) at the 25-3 leaf stage (cultivar Ni Nihonbare) with 1 * 2 trees after submersion and plowing. Then, the growth was managed in 3 to 4 cTL of water.

ノビエが2.5〜3葉と35〜4葉期の2時間に湛水4
C7TLで実施例30粒剤の所定量を処理した。
Flooding 4 for 2 hours when wildflowers have 2.5 to 3 leaves and 35 to 4 leaves.
A predetermined amount of Example 30 granules was treated with C7TL.

処理後30日目に残在植物体の生体重を測定し、下記式
に従って浅草量比をもって除草効果および薬害とした。
On the 30th day after the treatment, the fresh weight of the remaining plants was measured, and the herbicidal effect and herbicidal damage were expressed as the grass mass ratio according to the following formula.

を第3表(ノビエ2.5〜3葉期処理)および第4表(
ノビエ3.5〜4葉期処理)に示す。
Table 3 (Novie 2.5-3 leaf stage treatment) and Table 4 (
(3.5-4 leaf stage treatment).

第3表および第4表に示す通り本発明剤は、水稲に薬害
を及ぼすことなく、広い範囲の雑草防除に有効である。
As shown in Tables 3 and 4, the agent of the present invention is effective in controlling a wide range of weeds without causing any phytotoxicity to paddy rice.

しかも、対照区においては雑草が再生傾向にあるにもか
かわらず、本発明剤によれば雑草は完全に枯殺され、そ
の後の再生はみられない。
Furthermore, although the weeds tended to regenerate in the control plot, the inventive agent completely killed the weeds and no subsequent regeneration was observed.

Claims (1)

【特許請求の範囲】[Claims] 13・4−ジクロルプロピオンアニリド、βナフチル−
N〜メチルカーバメートおよび2−クロル−/・6′−
ジエチル−N−(7”)キシメチル)アセトアニリドを
含有することを特徴とする湛水田用除草剤。
13,4-dichloropropionanilide, β-naphthyl-
N~methyl carbamate and 2-chloro-/·6'-
A herbicide for use in flooded fields, characterized by containing diethyl-N-(7'')oxymethyl)acetanilide.
JP15281175A 1975-12-23 1975-12-23 Tansuiden Youjiyosouzai Expired JPS5827765B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15281175A JPS5827765B2 (en) 1975-12-23 1975-12-23 Tansuiden Youjiyosouzai

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15281175A JPS5827765B2 (en) 1975-12-23 1975-12-23 Tansuiden Youjiyosouzai

Publications (2)

Publication Number Publication Date
JPS5276431A JPS5276431A (en) 1977-06-27
JPS5827765B2 true JPS5827765B2 (en) 1983-06-11

Family

ID=15548658

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15281175A Expired JPS5827765B2 (en) 1975-12-23 1975-12-23 Tansuiden Youjiyosouzai

Country Status (1)

Country Link
JP (1) JPS5827765B2 (en)

Also Published As

Publication number Publication date
JPS5276431A (en) 1977-06-27

Similar Documents

Publication Publication Date Title
RU2029471C1 (en) Pyrimidine derivatives, herbicide composition, and a method of struggle against weed using composition
JPS6358818B2 (en)
JPS5827242B2 (en) Suiden Yojiyosouzaisoseibutsu
JPS5827765B2 (en) Tansuiden Youjiyosouzai
JPS608247A (en) Phthalamide derivative and agricultural and horticultural fungicide
JPS5827766B2 (en) Tansuiden Youjiyosouzai
JPS6261561B2 (en)
JPS6242883B2 (en)
JPS5839126B2 (en) Herbicidal composition
JPH03115205A (en) Herbicide composition
JPS6034902A (en) Herbicidal composition
JPS63225305A (en) Agricultural germicidal and plant growth regulating composition
JPH0256324B2 (en)
JPS6120521B2 (en)
JPS6366104A (en) Agent for reducing injury from salt and phytotoxicity of crop
JPS5820922B2 (en) Dojiyou Satsukinzai
JPH0314802B2 (en)
JPS63287704A (en) Herbicidal composition for paddy field
JPH02129105A (en) Herbicide for rice culture
JPS5940121B2 (en) Herbicide
JPS5827764B2 (en) Herbicide composition for paddy fields
JPH01294604A (en) Use of agricultural fungicide
JPS5912081B2 (en) Prunus elegans
JPH03106803A (en) Phytotoxicity relieving agent for herbicide used for rice plant
JPS63130504A (en) Phytotoxicity reducing agent for crop