JPS62111901A - Male sterilizing agent for plant - Google Patents

Male sterilizing agent for plant

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Publication number
JPS62111901A
JPS62111901A JP25172785A JP25172785A JPS62111901A JP S62111901 A JPS62111901 A JP S62111901A JP 25172785 A JP25172785 A JP 25172785A JP 25172785 A JP25172785 A JP 25172785A JP S62111901 A JPS62111901 A JP S62111901A
Authority
JP
Japan
Prior art keywords
active ingredient
plants
male
metal salt
sterilizing agent
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.)
Granted
Application number
JP25172785A
Other languages
Japanese (ja)
Other versions
JPH0699252B2 (en
Inventor
Masaharu Sakaki
榊 正治
Masato Mizutani
理人 水谷
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.)
Sumitomo Chemical Co Ltd
Original Assignee
Sumitomo 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 Sumitomo Chemical Co Ltd filed Critical Sumitomo Chemical Co Ltd
Priority to JP25172785A priority Critical patent/JPH0699252B2/en
Publication of JPS62111901A publication Critical patent/JPS62111901A/en
Publication of JPH0699252B2 publication Critical patent/JPH0699252B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:A male sterilizing agent for plants, containing a specific 1,2,4- triazine-3,5-dione derivative as an active ingredient and capable of readily and efficiently inducing male sterility by treating plants. CONSTITUTION:A male sterilizing agent for plants containing a 1,2,4-triazine-3,5- dione derivative expressed by formula I [R1 is H or formula II (R2 is alkyl or phenyl)] or a metal salt thereof, e.g. alkali metal salt such as Na or K, etc., alkaline earth metal salt such as Ca or Ba, etc., as on active ingredient. A carrier or adjuvant is mixed with the above-mentioned active ingredient and formulated into emulsion, wettable powder, suspension, granule, liquid solution, etc., for use. The amount of the active ingredient in the formulation is 0.1-90% weight ratio. The agent is useful for various cultivated crops, e.g. grains such as rice plant, wheat, corn, etc., leguminous crops such as soybean, etc., vegetables such as eggplant, tomato, cabbage, etc., flowering plants such as petunia, etc.

Description

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

本発明は、一般式〔υ 基またはフェニル基を表わす。)〕 で示されるi、2.4−)リアジン−8,5−ジオン誘
導体またはその金属塩を有効成分として含有する植物の
雄性不稔化剤に関するものである。 一般式[T]で示される1 、2.4−トリアジン−8
,5−ジオン誘導体の金属塩としては、たとえばナトリ
ウム、カリウム、リチウム等のアルカリ金属塩、力/L
/Vウム、バリウム、ストロンチウム等のアルカリ土類
金属塩等をあげることがで色る〇 近年食糧危機が叫ばれるようになり、その増産が大きな
課題となっている0そうした中で雑種第一代植物の生産
が注目を集めている0雑種第一代植物は、その旺盛な生
育によシ、両親の品種より収量が多くなる等多くの優れ
た形質を有することが知られている。雑種第一代種子を
得るためには、雌親の自家受粉を防ぐ必要があり、その
ためには雌親の雄蕊を取り除かねばならない◇ 従来この除雄作業は大変な労力を有1〜、また、イネ、
コムギのような自家受粉性の高い穀類で社小さな頴花内
に雄蕊、雄蕊があるため、手作業で仁れを行ない雑種拾
一種子を大量に生産することは、はとんど不可能であっ
た。また他の方法、たとえば細胞質雄性不稔の利用等が
あるが、とれもその育成に多大な年月を要する等の問題
点があシ、したがって雌の受粉能力を失わせず雄性不稔
を惹起する簡便かつ確実な方法が望まれているのが実状
である0 本発明者らは、長年にわたシ鋭意検討を重ねた結果、驚
くべきことに一般式〔工〕で示される1゜2.4−トリ
アジン−8,6−シオン誘導体またはその金属旭(以下
、単に本トリアジン誘導体と称する。)を植物に処埠す
ることにより。 ^わめで簡単に、効率よく雄性不稔を惹起し得ることを
見出し、本発明を完成するに至った0本トリアジン銹導
体は、たとえば特開昭56−100702号および56
−104874号各公報に記載の公知化a物である。 本発明の不稔化j111が適用できる対象植物と1〜て
は、たとえばイネ、コムギ、オオムギ、カラスムギ、ラ
イ麦、トウモロコシ等の穀類、ダイス等のマメ科作物、
ナヌ、トマト、キャベツ等の薩菜知、ペチュニア、画日
華等の花Il類等の種々の栽培植物をあげることができ
る〇以下に本トリアジン誘導体の具体例を示すが、もち
ろんこれらのみに限宇されるものではない。 第1表 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、水利剤、懸濁剤、粒剤、液剤等に製剤する。 これらの製剤には有効成分として本発明化合物を、重量
化で0.1〜90%、好ましくは1〜70%含有する〇 固体担体としては、カオリンフレ「、アッタバルジャイ
トクレー、ベントナイト、酸性白土、パイロフィライト
、り〜り、珪藻土、方解石、クルミ粉、尿素、硫酸アン
モニウム、合成含水酸化珪素吟の酸粉末あるいは粒状物
があげられ、治体担体としては、キVレン、メチルナフ
タレン等の芳香族炭化水素類、イソグロバノーμ、エチ
レングリコール、セロソルブ等のアルコール類、アセト
ン、Vりpヘギサノン、イソホロン等のケトン類、大豆
油、#M実油等の植物油、ジメチルスルホキVド、ア七
ト二トリル、水等がおばらねる。 乳化、分散、湿展等のために用いられる界面活性剤とし
ては、アルキル硫酸エステ)V塩、アルキルアリ−μス
ルホン酸塩、ジアルキpス〃ホコハク酸塩、ポリオキシ
エチレンアルキ〜アリールエーテ、A/リン酸エステ/
L’塩等の陰イオン界面活性剤、ポリオキシエチレンア
ルキルエーテル、ポリオキVエチレンアルキルアリール
エーテル、ポリオキVエチレンポリオキンプロピレンブ
ロックコボリマー、ソルビタン脂肪酸エステ〃、ホリオ
キVエチレンソルビタン脂肪酸エヌテ/V専の非イオン
界面活性剤尋があげられる。製剤用補助剤としては、リ
グニンスルホン酸塩、アルギン酸塩、ポリビニルアルコ
ール、アラビアガム、CMC(カルボキンメチルセルロ
ース)、PAP(酸性リン酸イソプロピ/L/)尋があ
げられる。 次に製剤例を示す◇なお、化合物は第1表の化合物番号
で示す0部は重量部を示す0製剤例1 化合物(1) 10部、リグニンスルホン酸カルンウム
8部、ヲウリ#硫酸ナトリウム2部および合成含水酸化
珪素86部をよく粉砕混合
The present invention represents the general formula [υ group or phenyl group]. )] The present invention relates to a male sterilizing agent for plants containing a riazine-8,5-dione derivative or a metal salt thereof as an active ingredient. 1,2,4-triazine-8 represented by general formula [T]
,5-dione derivatives include, for example, alkali metal salts such as sodium, potassium, and lithium;
/Vium, barium, strontium, and other alkaline earth metal salts can be added to the food supply.In recent years, food crises have become a hot topic, and increasing production has become a major issue.In such circumstances, the first generation of hybrids The first generation zero hybrid plants, which are attracting attention for plant production, are known to have many superior traits such as vigorous growth and higher yields than their parent varieties. In order to obtain first-generation hybrid seeds, it is necessary to prevent self-pollination of the female parent, and for this purpose, the stamens of the female parent must be removed. Conventionally, this emasculation process was very labor intensive. Rice,
Since wheat is a highly self-pollinating grain and has stamens and stamens within its small stamens, it is almost impossible to produce a large amount of hybrid seeds by manually cultivating the grains. there were. There are other methods, such as the use of cytoplasmic male sterility, but they all have the problem of requiring a long period of time to develop, and therefore do not cause male sterility without losing the female's ability to pollinate. In reality, there is a need for a simple and reliable method to do this.As a result of extensive research over many years, the present inventors surprisingly found that 1°2. By administering a 4-triazine-8,6-sion derivative or its metal derivative (hereinafter simply referred to as the present triazine derivative) to a plant. The zero-triazine conductor, which was discovered to be extremely easy and efficient to cause male sterility, and which led to the completion of the present invention, is disclosed in, for example, JP-A-56-100702 and JP-A-56-100702.
-104874 It is a known chemical compound a described in each publication. The target plants to which the sterilization j111 of the present invention can be applied include, for example, grains such as rice, wheat, barley, oats, rye, and corn; leguminous crops such as dice;
Various cultivated plants can be mentioned, such as Satsuma chili such as Nanu, tomatoes, and cabbage, and flowers such as petunia and Japanese flowers.Specific examples of the present triazine derivatives are shown below, but of course they are limited to only these. It's not something to be underestimated. It is mixed with a first surface carrier, a surfactant, and other formulation auxiliaries, and formulated into an emulsion, an aqueous solution, a suspension, a granule, a liquid, and the like. These preparations contain the compound of the present invention as an active ingredient in an amount of 0.1 to 90%, preferably 1 to 70% by weight. Examples of solid carriers include kaolin fret, attabulgite clay, bentonite, acid clay, Examples include acid powders or granules such as pyrophyllite, lily, diatomaceous earth, calcite, walnut powder, urea, ammonium sulfate, and synthetic hydrous silicon oxide. As a carrier, aromatic compounds such as xylene and methylnaphthalene are used. Hydrocarbons, alcohols such as isoglobanol, ethylene glycol, and cellosolve, ketones such as acetone, V-hegisanone, and isophorone, vegetable oils such as soybean oil and #M seed oil, dimethyl sulfoxide V-d, and acetate. Tolyl, water, etc. are available.Surfactants used for emulsification, dispersion, wet spreading, etc. include alkyl sulfate ester) V salts, alkylaryl-μ sulfonates, dialkylphosuccinates, Polyoxyethylene alkyl-arylethe, A/phosphoric acid ester/
Anionic surfactants such as L' salt, polyoxyethylene alkyl ether, polyoxyethylene alkyl aryl ether, polyoxyethylene polyoxine propylene block copolymer, sorbitan fatty acid ester, Horioki V ethylene sorbitan fatty acid Examples include ionic surfactants. Examples of formulation adjuvants include lignin sulfonate, alginate, polyvinyl alcohol, gum arabic, CMC (carboxylic methylcellulose), and PAP (isopropylene acid phosphate/L/). Next, a formulation example is shown◇Compounds are shown in the compound numbers in Table 1. 0 parts indicate parts by weight 0 Formulation Example 1 Compound (1) 10 parts, carunium ligninsulfonate 8 parts, Wouri #sodium sulfate 2 parts and 86 parts of synthetic hydrous silicon oxide are thoroughly ground and mixed.

【−で水和剤を得る○ 製剤例2 化合物(8) 10部、ポリオキシエチレンスチリルフ
ェニルエーテル】4部、ドデV、/1/ベンゼンスルホ
ン酸カルシウム6部およびVクロヘキサノン70部をよ
く混合して乳剤を得るQ製剤例8 化合物(2)2部、合成含水酸化珪素1部、リグニンス
A/ホン酸カルシウム2部、ベントナイト80部および
カオリンクレー65部をよく粉砕混合し、水を加えてよ
く練り合せた後、造粒乾燥して粒剤を得る。 製剤例4 化合物(8125部、ポリオキVエチレンソルビタンモ
ノオレエート8部、0M08部および水69部を混合し
、粒度が5ミクロン以下になるオで湿式粉砕して懸濁剤
を得る0製剤例5 化合物(1) 、 (2)各1部、ポリオギシエチレン
スチリルフェニルエーテ/l/1部および水98部を混
合し、1溶解して各々の液剤を得る0本不稔化剤を実際
に用いる場合、その処理方法としては、茎葉処理、土埃
処理専があり、その処理量は、対象作物、処理方法、処
理時期、環境条件、製剤形態専によっても異なるが、通
常は0.005〜10 rFg/ha、好ましくは0,
02〜8 Vhaである。処理時期は倉これも対象作物
、処理方法、環境条件、処理量、製剤形態等によっても
異なるが、好ましくは学殖生長開始前から開花直前の間
で処理される0 乳剤、水利剤、懸濁剤、←奸液剤等は、通常その所定量
を1アー/I/あたシロ。5リット/l/〜20リット
ルの(必要ならば、展着剤等の補助剤を添加した)水で
希釈して処理し、粒剤等は、通常なんら希釈することな
くそのまま処理する0展着剤としては、前記の界面活性
剤のほか、ポリオキンエチレン樹脂酸(エステ/I/)
、リクニンスルホン酸塩、アビエチン酸塩、ジナフチル
メタンジスルホン酸塩、パラフィン醇があげられる。 また他の植物、生育詞節剤、除草剤、殺虫剤、殺ダニ剤
、殺線虫剤、殺菌剤、肥料、土壌改良剤停と混合して用
いることもできる。 さらに雑種種子を大量に得るためには、一般的に次の方
法が適している0すなわち、かけ合わせようとする2つ
の親を交互に植える。このとき名々の親の条数、幅は、
その作物の種、品種およびその環境条件等によって異な
る。そして雌親に本トリアジン誘導体を処理し、雄性不
稔となった雌親は、他方の雄性活性のある雄親の花粉を
受粉し、雑種種子が得られる0純粋な雑種第一代種子を
得ようとする場合は、本トリアジン誘導体を処理し、雄
性不稔となった雌親に、開花前に袋かけをし、他家受粉
を防ぎ、開花後雄性徳性のある雄親の花粉を直接人為的
に交配し、再び袋をかけ直す方法が好ましい0次に試験
例をあげ、本発明をさらに詳細に説明する0な2、化合
物は、第1表に記載の化合物番号で示す。 培土を詰めたものにコムギ(品種:農林61号)を播種
し、胤温り7℃−夜温20℃(15時間日長、袖光有り
0)温室条件−トで育てた◎その後、出穂始期よシ0〜
1.7〜8および14〜15日lIJの8回、同一ポッ
トに供試化合物を乳剤′または液剤に製剤し、その所定
量を展着剤を含む水で希釈したものを1アールあた。?
10!Jットルの液誌で、小型rIA霧酩を用い、植物
体の」1力から茎葉処理した〇出穂後開花前にポットあ
たり4穂に袋をかけて他家受粉を防き′、登熟後、表を
かけた穂について、小穂数、種子数を1査し、出穂あた
り種子数の対無処埠区比百分率で各化合物の不稔性を示
した(第2表)0 (lO) 第   2   表 試験例2 コムギにおける雌性徳性の確認−(1例1と
同様に、コムギ農林61号を育成し九〇その後出穂始期
よpb日または11日前の2凹、液剤に供試化合物を製
剤し、そのh宏量をkm剤を含む水で希釈したものを1
7−)Vめた910リットルの液量で、小型噴霧器を用
い、植物体の上方から茎葉処理した0出穂後lポv1あ
ftcシ4穂に訣かけを行なっだ◇まだ、開花後表かけ
を行なりでいない穂4穂について、薬剤無処理区からと
って子数を調査し、出穂あ九シ神子数の対無処理区比百
分率を示した(第8表)0袋かけを行なった穂よりも交
配を行なった穂の方がその値が高ければ、雄性不稔性を
持ちながら雌性を 稔性走保っていることを示すものである。 @8表 試験例8 イネにおける不稔性の発史 イネ(品種;コシヒカリ)を人工培土に播挿し、播種後
20日に1/10,000アールのポットに苗を植え湛
水状態とした。その後出穂始期前20日、18日または
6日の8回、液剤に供試化合物を製剤し、その所定菫を
展着剤を含む水で希釈したもOを17−ルあたp1θリ
ットルの液量で、小型噴霧器を用い、植物体の上方から
茎葉処理した0出穂後ポツトあたシロ穂に繊をかけて他
家受粉を防すだ。登熟後、袋をかけた穂について、顧花
数、種子数を調査し、頴花数あたシ種子数の対無処理区
比百分率で不稔性を示した(第4表)0試験は屋外条件
下、2反復で行なった〇 第    4    表 (1B完)
[Obtain a wettable powder with -○ Formulation Example 2 Compound (8) 10 parts, polyoxyethylene styrylphenyl ether] 4 parts, Dode V, /1/calcium benzenesulfonate 6 parts and V clohexanone 70 parts Q Formulation Example 8 to obtain an emulsion by mixing 2 parts of compound (2), 1 part of synthetic hydrated silicon oxide, 2 parts of lignin A/calcium phonate, 80 parts of bentonite and 65 parts of kaolin clay were thoroughly ground and mixed, and water was added. After thoroughly kneading the mixture, the mixture is granulated and dried to obtain granules. Formulation Example 4 Mix 8125 parts of the compound, 8 parts of Polyoxy V ethylene sorbitan monooleate, 8 parts of 0M0, and 69 parts of water, and wet-pulverize in an oven to give a particle size of 5 microns or less to obtain a suspension. Formulation Example 5 Mix 1 part each of compounds (1) and (2), 1 part polyoxyethylene styrylphenyl ether/1 part and 98 parts water and dissolve 1 part to obtain each liquid agent. 0 Sterilizing agents are actually used. In this case, treatment methods include foliage treatment and dirt treatment, and the treatment amount varies depending on the target crop, treatment method, treatment time, environmental conditions, and formulation form, but is usually 0.005 to 10 rFg. /ha, preferably 0,
02-8 Vha. The treatment timing varies depending on the target crop, treatment method, environmental conditions, amount of treatment, formulation form, etc., but it is preferably treated between before the start of academic growth and just before flowering.0 Emulsions, irrigation agents, suspensions For agents, ← liquid agents, etc., the prescribed amount is usually 1 ar/I/at Shiro. Diluted with 5 liters/l/~20 liters of water (adding auxiliary agents such as a spreading agent if necessary) and processed. Granules, etc. are usually processed as they are without any dilution. In addition to the above-mentioned surfactants, examples of agents include polyoxine ethylene resin acid (Este/I/)
, likunin sulfonate, abietate, dinaphthylmethane disulfonate, and paraffin sauce. It can also be used in combination with other plants, growth regulators, herbicides, insecticides, acaricides, nematicides, fungicides, fertilizers, and soil conditioners. In order to further obtain large quantities of hybrid seeds, the following method is generally suitable: alternating planting of the two parents to be crossed. At this time, the number and width of the famous parents are
It varies depending on the species, variety, and environmental conditions of the crop. Then, the female parent is treated with this triazine derivative, and the female parent, which has become male sterile, is pollinated with the pollen of the other male parent with male activity to obtain pure hybrid first generation seeds. If you wish to use this triazine derivative, the male sterile female parent should be covered with a bag before flowering to prevent cross-pollination, and after flowering the pollen of the male parent, which has male virility, can be directly harvested. It is preferable to cross-breed and re-bag it again. Next, test examples will be given to explain the present invention in more detail. Compounds are indicated by the compound numbers listed in Table 1. Wheat (variety: Norin No. 61) was sown in a soil filled with soil, and grown under greenhouse conditions with a seed temperature of 7℃ and a night temperature of 20℃ (15-hour photoperiod, no side light). The beginning is 0~
The test compound was formulated into an emulsion or solution in the same pot eight times from 1.7 to 8 and 14 to 15 days lIJ, and a predetermined amount of it was diluted with water containing a spreading agent per 1 are. ?
10! In J.T.L.'s liquid journal, we used a small rIA mist to treat the stems and leaves from the plant body. After heading and before flowering, we placed bags on 4 ears per pot to prevent cross-pollination, and after ripening. The number of spikelets and number of seeds were examined for the eared ears, and the sterility of each compound was shown by the percentage of the number of seeds per ear compared to the untreated area (Table 2) 0 (lO) Table 2 Test Example 2 Confirmation of female virtue in wheat - (1 Similar to Example 1, wheat Norin No. 61 was grown, and the test compound was formulated into a liquid preparation on the PB day or 11 days before the beginning of heading. Then, dilute the h volume with water containing km agent and make 1
7-) Using a small sprayer with a liquid volume of 910 liters, sprayed the leaves from above the plant. For the 4 panicles that had not been treated, the number of offspring was investigated from the area without chemical treatment, and the percentage of the number of offspring in the ear compared to the area without treatment was shown (Table 8). 0 bags were applied. If the value is higher in the hybridized panicle than in the panicle, it indicates that the hybridized panicle maintains female fertility even though it has male sterility. @Table 8 Test Example 8 Sterile rice (variety: Koshihikari) was sown in artificial soil, and 20 days after sowing, seedlings were planted in 1/10,000 are pots and flooded. Thereafter, the test compound was prepared in a liquid preparation eight times on the 20th, 18th, or 6th day before the beginning of heading, and the specified violet was diluted with water containing a spreading agent. To prevent cross-pollination, use a small sprayer to apply fibers from above the plants to the white panicles of the pot after earing. After ripening, the bagged ears were investigated for the number of flowers and seeds, and sterility was shown as a percentage of the number of flowers and seeds compared to the untreated plot (Table 4) 0 test Table 4 (Complete 1B)

Claims (1)

【特許請求の範囲】 一般式 ▲数式、化学式、表等があります▼ 〔式中、R_1は水素原子または式▲数式、化学式、表
等があります▼で示される基を表わす。(ここにR_3
はアルキル基またはフェニル基を表わす。)〕 で示される1,2,4−トリアジン−8,5−ジオン誘
導体またはその金属塩を有効成分として含有することを
特徴とする植物の雄性不稔化剤。
[Claims] General formula▲There are numerical formulas, chemical formulas, tables, etc.▼ [In the formula, R_1 represents a hydrogen atom or a group represented by the formula▲There are numerical formulas, chemical formulas, tables, etc.▼. (R_3 here
represents an alkyl group or a phenyl group. )] A male sterilizing agent for plants, comprising a 1,2,4-triazine-8,5-dione derivative or a metal salt thereof as an active ingredient.
JP25172785A 1985-11-08 1985-11-08 Plant male sterility agent Expired - Lifetime JPH0699252B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP25172785A JPH0699252B2 (en) 1985-11-08 1985-11-08 Plant male sterility agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP25172785A JPH0699252B2 (en) 1985-11-08 1985-11-08 Plant male sterility agent

Publications (2)

Publication Number Publication Date
JPS62111901A true JPS62111901A (en) 1987-05-22
JPH0699252B2 JPH0699252B2 (en) 1994-12-07

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Family Applications (1)

Application Number Title Priority Date Filing Date
JP25172785A Expired - Lifetime JPH0699252B2 (en) 1985-11-08 1985-11-08 Plant male sterility agent

Country Status (1)

Country Link
JP (1) JPH0699252B2 (en)

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Publication number Publication date
JPH0699252B2 (en) 1994-12-07

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