JPS637521B2 - - Google Patents
Info
- Publication number
- JPS637521B2 JPS637521B2 JP17851181A JP17851181A JPS637521B2 JP S637521 B2 JPS637521 B2 JP S637521B2 JP 17851181 A JP17851181 A JP 17851181A JP 17851181 A JP17851181 A JP 17851181A JP S637521 B2 JPS637521 B2 JP S637521B2
- Authority
- JP
- Japan
- Prior art keywords
- axillary
- buds
- tobacco
- axillary buds
- oil
- 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
Links
- 235000002637 Nicotiana tabacum Nutrition 0.000 claims description 23
- 244000061176 Nicotiana tabacum Species 0.000 claims description 22
- 239000008158 vegetable oil Substances 0.000 claims description 22
- 235000015112 vegetable and seed oil Nutrition 0.000 claims description 19
- 238000000034 method Methods 0.000 claims description 6
- 241000208125 Nicotiana Species 0.000 claims 1
- OEYOMNZEMCPTKN-UHFFFAOYSA-N Butamifos Chemical compound CCC(C)NP(=S)(OCC)OC1=CC(C)=CC=C1[N+]([O-])=O OEYOMNZEMCPTKN-UHFFFAOYSA-N 0.000 description 14
- 239000000839 emulsion Substances 0.000 description 14
- 230000000694 effects Effects 0.000 description 9
- 235000019484 Rapeseed oil Nutrition 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 235000019198 oils Nutrition 0.000 description 8
- 238000001035 drying Methods 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- -1 maleic hydrazide choline salt Chemical class 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- 230000018109 developmental process Effects 0.000 description 5
- 241000196324 Embryophyta Species 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- 239000003112 inhibitor Substances 0.000 description 3
- 230000005764 inhibitory process Effects 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 3
- 238000007865 diluting Methods 0.000 description 2
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 2
- 238000009313 farming Methods 0.000 description 2
- 238000003306 harvesting Methods 0.000 description 2
- 230000002401 inhibitory effect Effects 0.000 description 2
- 229940070765 laurate Drugs 0.000 description 2
- 229920000259 polyoxyethylene lauryl ether Polymers 0.000 description 2
- 230000001629 suppression Effects 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 230000002195 synergetic effect Effects 0.000 description 2
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- FOWAVPREFGTTQS-UPHRSURJSA-N (z)-4-hydrazinyl-4-oxobut-2-enoic acid Chemical class NNC(=O)\C=C/C(O)=O FOWAVPREFGTTQS-UPHRSURJSA-N 0.000 description 1
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
- DFAPRMLPEMDQIB-ODZAUARKSA-N 2-aminoethanol (Z)-4-hydrazinyl-4-oxobut-2-enoic acid Chemical compound NCCO.NNC(=O)\C=C/C(O)=O DFAPRMLPEMDQIB-ODZAUARKSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000283690 Bos taurus Species 0.000 description 1
- 239000004381 Choline salt Substances 0.000 description 1
- 239000005983 Maleic hydrazide Substances 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 230000028446 budding cell bud growth Effects 0.000 description 1
- 239000010495 camellia oil Substances 0.000 description 1
- 235000019417 choline salt Nutrition 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000010411 cooking Methods 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000008157 edible vegetable oil Substances 0.000 description 1
- 230000002708 enhancing effect Effects 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- GUXIZAVQQBQIJF-ODZAUARKSA-M potassium (Z)-4-hydrazinyl-4-oxobut-2-enoate Chemical compound [K+].C(\C=C/C(=O)[O-])(=O)NN GUXIZAVQQBQIJF-ODZAUARKSA-M 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 238000007711 solidification Methods 0.000 description 1
- 230000008023 solidification Effects 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明はたばこ腋芽防止方法に関するものであ
り、次式
で示されるO−エチル−O−(2−ニトロ−5−
メチルフエニル)−N−セカンダリ−ブチルホス
ホロアミドチオネートを植物油と配合してたばこ
植物に施用することを特徴とする。
本発明方法は、単に効力を増強して薬量を節減
する効果ばかりでなく、数センチに伸長した腋芽
をも枯殺し、また雨天続きでも効力を低下するこ
となく2次芽、3次芽の発生を完全に抑止するの
で腋芽防止に関する労力を著しく軽減する効果を
有するものである。
たばこ作には苗床作業、本畑作業のほか収穫後
の乾燥、調理など多くの手間と時間を要する作業
があるが、繁忙期を圧迫するものとして収穫まぎ
わの腋芽除去作業がある。この作業は葉たばこの
収量と品質を確保するうえで必要不可決である
が、これを手作業でするとなると次々と出てくる
腋芽を3日にあげずとりまわらなければならなく
なる。このようなことから腋芽防止剤を散布する
方法が開発され普及している。
現在、わが国において実用化されているたばこ
腋芽防止剤は、マレイン酸ヒドラジツドエタノー
ルアミン塩、マレイン酸ヒドラジツドカリウム
塩、マレイン酸ヒドラジツドコリン塩であるが、
これらの薬剤は施用濃度が比較的高濃度で時と
してたばこの品質低下をきたすことおよび耐雨
性が不充分で雨天が続くと効力不足問題を起すこ
とが問題点としてあげられている。実際問題とし
て、たばこの腋芽発生期は梅雨期にあたるので雨
天続きのことが多く、このため従来の腋芽防止剤
は耐雨性の不足により効力を失い、2次芽、3次
芽の出芽を抑えることができず、手作業でとりま
わることになる。また、腋芽発生期に雨天が続く
と薬剤散布ができないために散布適期を逸し、散
布時には腋芽はすでに数センチ伸長していること
が多い。このようなことから耐雨性にすぐれ、し
かもすでに伸長した腋芽を成葉に悪影響を与えず
に選択的に枯殺できる腋芽防止剤の出現が強く望
まれている。
本発明者らは、このような要望にこたえるべく
研究に取組んできたのであるが、O−エチル−O
−(2−ニトロ−5−メチルフエニル)−N−セカ
ンダリーブチルホスホロアミドチオネート(以下
ブタミホスと記す。)に植物油を配合してたばこ
植物に施用すると、驚くべき協力効果が発現する
ことを知見し、その目的に適合することを確認し
て本発明に到達したのである。
ブタミホスがたばこの腋芽防止に有効であるこ
とは、特公昭53−12980号公報により公知である。
ブタミホスは上記公報に記載のとおり、ポツト栽
培された無降雨条件下におけるたばこ腋芽に対し
ては、施用濃度500ppmの低濃度水稀釈液の散布
によつて、高い腋芽成長抑止効果を示す。しか
し、一般農家の行う降雨条件下の圃場に定植した
たばこの腋芽防止に試験して見ると、2000〜
3000ppmの高濃度条牛において発生初期の腋芽に
対してある程度効果が見られるが、5〜6cmに伸
長した腋芽に対しては効果なく、また散布直後の
降雨によつて効力は相当低下する。
他方、植物油がたばこの腋芽防止にある程度有
効であることも公知で、かつて南九州地方の農村
で伝承的に使用されたといわれており、これに注
目した研究報告〔村岡洋三、大堀和信、岡山たば
こ試験場報告、第12号(昭和31年)1頁〜10頁〕
がある。
本報告によると、なたね油を60%乳化液にして
その原液を2倍に稀釈してたばこの腋芽部分に塗
布すると有効であつたと記載されている。しかし
ながら、植物油をかかる高濃度の乳化液にして腋
芽部分に付着させる方法は実用的に望ましいので
はなく、マレイン酸ヒドラジツド塩などの出現と
ともに忘れ去られたようである。本発明者らが実
験的に検討したところでは、植物油乳化液を水で
稀釈して散布した場合の効果は高いものではな
く、油分10%以下に稀釈すると腋芽防止効果はき
わめて低いものであつた。
しかるに本発明に従つて、単独ではたばこ腋芽
防止剤として実用効果の得られない濃度のブタミ
ホス液に、腋芽防止効果をほとんど示さない程度
の量の植物油を配合して施用すると、驚くべき協
力効果を発揮して発生初期腋芽の伸長阻止はもち
ろん、すでに伸長した腋芽を故殺し、耐雨性を著
しく向上して2次芽、3次芽の発生を完全にない
しほぼ完全に抑止することができ、他方成葉には
何ら薬害がみられない。
植物油はその固化性の強弱によつて乾性油(あ
まに油、えの油、きり油など)、半乾性油(ごま
油、なたね油、綿実油、大豆油など)、不乾性油
(つばき油、オリーブ油、ひまし油など)に分類
されるが、本発明に用いる植物油の種類は、実施
例3に例示しているように効力増強の面からは乾
性油、半乾性油、不乾性油のいずれを用いてもよ
い。これらの中で実用的にはなたね油が適当であ
るが、実用性は植物油の価格、入手性などの要因
によつて変化するので本発明に用いる植物油の種
類は限定されない。
本発明でたばこ植物に施用するブタミホス−植
物油配合液の濃度は、特に限定されないが、ブタ
ミホスについては250〜2000ppm、より好ましく
は500〜2000ppm、植物油については0.5〜10%、
より好ましくは1〜5%で用いられる。ブタミホ
ス濃度が低いときは植物油濃度は高くするのがよ
く、ブタミホス濃度が高いときは植物油濃度は低
くてもよい。
これら配合濃度、割合はたばこの品種、腋芽の
発生状況、天候、施用時期などにより適当に決め
られるべきものであるが、前記の範囲内で充分に
本発明の効果が具現される。
ブタミホス−植物油配合液のたばこ植物への施
用は、通常、腋芽発生部位に対して散布する方法
がとられるが、もちろん塗布によることもでき
る。一般に腋芽防止効果は、無施用株の腋芽伸長
量に対する抑制率で示され、実用的には95%以上
の水準が望まれる。本発明によれば、降雨条件下
においてかつ比較的低濃度のブタミホス液をもつ
て、容易にこの水準を超え、実用的にはほぼ完全
に腋芽の抑止が可能である。
ブタミホスに植物油を配合する方法はきわめて
容易である。すなわちブタミホス乳剤を所望の濃
度に水にうすめた液に一定濃度たとえば90%に調
製した植物油乳剤を添加撹拌することによつて行
われる。
ブタミホスは植物油と相溶性を有するので溶剤
に植物油を用いて適当な界面活性剤を添加してブ
タミホス−植物油混合乳剤を製剤化することによ
つても本発明を実施することができる。本乳剤の
製剤化法については実施例4に1部を例示したと
おり、非イオン界面活性剤やアニオン界面活性剤
または両者の混合物を用いる公知の方法によつて
容易に行うことができる。
以下に本発明の内容と効果をより明らかにする
ために実施例をあげて説明する。
実施例 1
圃場に定植栽培したタバコ(品種BY−4号)
が開花初期になつた時、3cm以上生育した腋芽と
頂芽をつみとり、各供試薬剤の水稀釈液およびナ
タネ油との混合液を株当り20ml小型ハンドスプレ
ーにて腋芽発生部位に散布処理した。処理30日後
に発生している腋芽を摘みとりその腋芽生重量を
測定した。そして、1腋芽重を求めて下式によつ
て抑制率を求め第1表に示した。
腋芽抑制率(%)={1−処理区の1腋芽当りの生
重量/無処理区の1腋芽当りの生重量}×100
The present invention relates to a method for preventing tobacco axillary buds, which is performed using the following formula: O-ethyl-O-(2-nitro-5-
The present invention is characterized in that methylphenyl)-N-secondary-butylphosphoroamidothionate is blended with vegetable oil and applied to tobacco plants. The method of the present invention not only enhances efficacy and reduces drug dosage, but also kills axillary buds that have grown several centimeters in length, and also kills secondary and tertiary buds without decreasing efficacy even in continuous rainy weather. Since it completely inhibits the occurrence of axillary buds, it has the effect of significantly reducing the labor involved in preventing axillary buds. Tobacco farming involves many labor-intensive and time-consuming tasks such as nursery work, main field work, and post-harvest drying and cooking, but one thing that puts pressure on the busy season is removing the axillary buds right before the harvest. This work is necessary to ensure the yield and quality of leaf tobacco, but if it were done by hand, the axillary buds would have to be removed one after another within three days. For this reason, a method of spraying an axillary bud inhibitor has been developed and is becoming popular. The tobacco axillary bud inhibitors currently in practical use in Japan are maleic hydrazide ethanolamine salt, maleic hydrazide potassium salt, and maleic hydrazide choline salt.
Problems with these agents include that the applied concentration is relatively high, which sometimes causes a deterioration in the quality of tobacco, and that they have insufficient rain resistance, resulting in insufficient efficacy when rain continues. As a practical matter, the axillary bud generation period of tobacco falls during the rainy season, so there are many rainy days, so conventional axillary bud prevention agents lose their effectiveness due to lack of rain resistance and suppress the emergence of secondary and tertiary buds. It is not possible to do so, and it has to be done manually. In addition, if it continues to rain during the axillary bud development period, the appropriate time for spraying will be missed because it will not be possible to spray the chemical, and the axillary buds will often have already grown several centimeters by the time they are sprayed. For this reason, there is a strong desire for an axillary bud inhibitor that has excellent rain resistance and can selectively kill already elongated axillary buds without adversely affecting adult leaves. The present inventors have been engaged in research to meet these demands, and found that O-ethyl-O
It has been discovered that when -(2-nitro-5-methylphenyl)-N-secondary butyl phosphoroamidothionate (hereinafter referred to as butamiphos) is blended with vegetable oil and applied to tobacco plants, a surprising synergistic effect appears. The present invention was arrived at after confirming that it was suitable for that purpose. It is known from Japanese Patent Publication No. 53-12980 that butamiphos is effective in preventing axillary buds of tobacco.
As described in the above-mentioned publication, butamiphos exhibits a high axillary bud growth inhibiting effect on tobacco axillary buds grown in pots under rainless conditions by spraying a low-concentration diluted solution in water at an application concentration of 500 ppm. However, when tested by general farmers to prevent axillary buds from tobacco planted in fields under rainfall conditions, it was found that
In row cattle at a high concentration of 3000 ppm, some effect is seen on axillary buds in the early stages of development, but it is not effective on axillary buds that have grown to 5 to 6 cm, and the efficacy is considerably reduced by rain immediately after spraying. On the other hand, it is well known that vegetable oil is effective to some extent in preventing the axillary buds of tobacco, and is said to have been traditionally used in farming villages in the southern Kyushu region. Test site report, No. 12 (1955) pages 1-10]
There is. According to this report, it was stated that it was effective to make a 60% emulsion of rapeseed oil, dilute the stock solution twice, and apply it to the axillary buds of tobacco. However, the method of making such a highly concentrated emulsion of vegetable oil and applying it to the axillary buds is not practically desirable and seems to have been forgotten with the advent of maleic acid hydrazide salts. According to the experimental studies carried out by the present inventors, the effect of diluting a vegetable oil emulsion with water and spraying it was not high, and that when diluted to an oil content of 10% or less, the effect of preventing axillary buds was extremely low. . However, according to the present invention, when a butamiphos solution with a concentration that does not have a practical effect as a tobacco axillary bud-preventing agent alone is mixed with a vegetable oil in an amount that shows almost no axillary bud-preventing effect and applied, a surprising synergistic effect is obtained. Not only can it inhibit the elongation of axillary buds in the early stages of development, but it can also kill axillary buds that have already elongated, significantly improving rain resistance and completely or almost completely inhibiting the development of secondary and tertiary buds. No chemical damage is observed in the adult leaves. Vegetable oils are classified into drying oils (linseed oil, edible oil, tung oil, etc.), semi-drying oils (sesame oil, rapeseed oil, cottonseed oil, soybean oil, etc.), and non-drying oils (camellia oil, olive oil, etc.) depending on their solidification strength. However, as illustrated in Example 3, the type of vegetable oil used in the present invention may be drying oil, semi-drying oil, or non-drying oil, from the standpoint of enhancing efficacy. good. Among these, rapeseed oil is suitable for practical use, but the type of vegetable oil used in the present invention is not limited since the practicality varies depending on factors such as the price and availability of the vegetable oil. The concentration of the butamiphos-vegetable oil mixture applied to tobacco plants in the present invention is not particularly limited, but for butamiphos it is 250 to 2000 ppm, more preferably 500 to 2000 ppm, and for vegetable oil it is 0.5 to 10%.
More preferably, it is used in an amount of 1 to 5%. When the butamiphos concentration is low, the vegetable oil concentration may be high, and when the butamiphos concentration is high, the vegetable oil concentration may be low. These concentrations and ratios should be appropriately determined depending on the variety of tobacco, the state of development of axillary buds, the weather, the time of application, etc., but the effects of the present invention can be fully realized within the above ranges. The butamiphos-vegetable oil mixture is usually applied to tobacco plants by spraying it on the axillary bud formation site, but of course it can also be applied by coating. Generally, the effect of preventing axillary buds is expressed by the inhibition rate against the amount of axillary bud elongation of untreated plants, and practically a level of 95% or more is desired. According to the present invention, this level can be easily exceeded under rainy conditions and with a relatively low concentration of butamiphos solution, and practically it is possible to almost completely suppress axillary buds. The method of blending vegetable oil with butamifos is extremely easy. That is, it is carried out by diluting a butamiphos emulsion in water to a desired concentration and adding and stirring a vegetable oil emulsion prepared to a certain concentration, for example, 90%. Since butamiphos is compatible with vegetable oil, the present invention can also be carried out by using vegetable oil as a solvent and adding a suitable surfactant to formulate a butamiphos-vegetable oil mixed emulsion. The present emulsion can be easily formulated by a known method using a nonionic surfactant, an anionic surfactant, or a mixture of the two, as exemplified in part in Example 4. EXAMPLES Examples will be given below to clarify the content and effects of the present invention. Example 1 Tobacco planted and cultivated in the field (variety BY-4)
At the beginning of flowering, the axillary buds and apical buds that had grown over 3 cm were picked, and a mixture of each test chemical diluted in water and rapeseed oil was sprayed on the site where the axillary buds appeared using a small hand sprayer (20 ml per plant). did. After 30 days of treatment, the axillary buds that had developed were picked and the fresh weight of the axillary buds was measured. Then, the weight of one axillary bud was determined, and the inhibition rate was determined using the following formula and is shown in Table 1. Axillary bud suppression rate (%) = {1-fresh weight per axillary bud in treated area/fresh weight per axillary bud in untreated area} x 100
【表】
塩を使用した。
実施例 2
圃場に定植栽培したタバコ(バーレ−21号)が
開花盛期になつた時期に頂芽と1次腋芽をつみと
り、その後2次腋芽が1cm程度に生育した時期に
ブタミホス乳剤の水稀釈液とナタネ油乳剤の水稀
釈液をそれぞれ1:1に混合した所定濃度液を腋
芽発生部位に株当り20ml散布処理した。処理30日
後に発生している腋芽を摘みとり、実施例1同様
に抑制率を求め第2表に示した。[Table] Salt was used.
Example 2 The apical buds and primary axillary buds of tobacco (Burley No. 21) planted and cultivated in the field were harvested when they reached the peak flowering stage, and then when the secondary axillary buds had grown to about 1 cm, water containing Butamiphos emulsion was added. A predetermined concentration solution prepared by mixing the diluted solution and the water diluted solution of rapeseed oil emulsion at a ratio of 1:1, respectively, was sprayed at 20 ml per plant onto the axillary bud generation site. The axillary buds that had developed 30 days after the treatment were picked, and the inhibition rate was determined in the same manner as in Example 1 and is shown in Table 2.
【表】
雨あり。
実施例 3
圃場に定植栽培したタバコ(BY−4号)が開
花初期になつた時、3cm以上に生育した腋芽と頂
芽をつみとり、ブタミホス乳剤の500ppm液に各
植物油乳剤を2.3%濃度になるように混入撹拌し
た乳化液を株当り20ml小型ハンドスプレーにてタ
バコの腋芽部位に散布した、処理30日後に前記実
施例1同様に腋芽生体重を測定し、抑制率を求め
ると同時に有用な葉に対する薬害を観察し第3表
に示した。[Table] Rain.
Example 3 When the tobacco grown in the field (BY-4) reached the early stage of flowering, the axillary buds and apical buds that had grown to 3 cm or more were picked, and each vegetable oil emulsion was added to a 500 ppm solution of Butamiphos emulsion at a concentration of 2.3%. The emulsion was mixed and stirred so that 20ml per plant was sprayed on the axillary buds of the tobacco plants using a small hand sprayer. 30 days after the treatment, the fresh weight of the axillary buds was measured in the same manner as in Example 1, and at the same time the suppression rate was determined. The chemical damage to the leaves was observed and shown in Table 3.
【表】【table】
【表】
実施例 4
(1) O−エチル−O−(2−ニトロ−5−メチル
フエニル)−N−セカンダリーブチルホスホロ
アミドチオネート50部、キシレン35部およびポ
リオキシエチルラウリルエーテル(界面活性
剤)15部を均一に混和してブタミホス乳剤とし
た。
(2) ナタネ白紋油90部、オレイン酸1部、ポリオ
キシエチレンノニルフエニルエーテル4部、ポ
リグリセライドラウレート3部およびポリオキ
シエチレンラウリルエーテル2部を均一に混和
してナタネ油乳剤とした。
(3) O−エチル−O−(2−ニトロ−5−メチル
フエニル)−N−セカンダリーブチルホスホロ
アミドチオネート5部、ナタネ白紋油85部、ポ
リオキシエチレンノニルフエニルエーテル4
部、ポリグリセライドラウレート3部およびポ
リオキシエチレンラウリルエーテル3部を均一
に混和してブタミホス−ナタネ油混合製剤とし
た。[Table] Example 4 (1) 50 parts of O-ethyl-O-(2-nitro-5-methylphenyl)-N-secondary butyl phosphoramidothionate, 35 parts of xylene and polyoxyethyl lauryl ether (surfactant) ) were uniformly mixed to form a butamiphos emulsion. (2) A rapeseed oil emulsion was prepared by uniformly mixing 90 parts of rapeseed oil, 1 part of oleic acid, 4 parts of polyoxyethylene nonyl phenyl ether, 3 parts of polyglyceride laurate, and 2 parts of polyoxyethylene lauryl ether. . (3) 5 parts of O-ethyl-O-(2-nitro-5-methylphenyl)-N-secondary butyl phosphoramidothionate, 85 parts of rapeseed oil, 4 parts of polyoxyethylene nonyl phenyl ether
1 part, 3 parts of polyglyceride laurate, and 3 parts of polyoxyethylene lauryl ether were uniformly mixed to prepare a butamiphos-rapeseed oil mixed preparation.
Claims (1)
フエニル)−N−セカンダリ−ブチルホスホロア
ミドチオネートを植物油と配合してたばこ植物に
施用することを特徴とするたばこ腋芽防止方法。1. A method for preventing tobacco axillary buds, which comprises applying O-ethyl-O-(2-nitro-5-methylphenyl)-N-secondary-butylphosphoroamidothionate to tobacco plants in combination with vegetable oil.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17851181A JPS5879910A (en) | 1981-11-06 | 1981-11-06 | Sucker control of tobacco |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17851181A JPS5879910A (en) | 1981-11-06 | 1981-11-06 | Sucker control of tobacco |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5879910A JPS5879910A (en) | 1983-05-13 |
JPS637521B2 true JPS637521B2 (en) | 1988-02-17 |
Family
ID=16049744
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17851181A Granted JPS5879910A (en) | 1981-11-06 | 1981-11-06 | Sucker control of tobacco |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5879910A (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN103190397A (en) * | 2013-04-02 | 2013-07-10 | 红云红河烟草(集团)有限责任公司 | Tobacco axillary bud inhibitor additive and application thereof |
CN105850997B (en) * | 2016-03-30 | 2018-04-20 | 贵州省烟草公司铜仁市公司 | Potassium nitrate starches tobacco germination inhibitor and its application process |
-
1981
- 1981-11-06 JP JP17851181A patent/JPS5879910A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5879910A (en) | 1983-05-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US20030224938A1 (en) | Enhanced herbicides | |
AU2023203117B2 (en) | 1-amino-1-cyclopropanecarboxylic acid hudrochloride formulations | |
JP2009545517A (en) | Silicone surfactant-based agricultural preparation and method of use thereof | |
JPH10251104A (en) | Insecticidal and acaricidal composition and insecticidal and acaricidal method | |
JP2771694B2 (en) | Post-emergence herbicidal composition comprising acetoxy-terminated silicone glycol and dispersant | |
EA015384B1 (en) | Herbicidal mixture, comprising an imidazolinone herbicide and an adjuvant | |
US4182621A (en) | Composition for inhibiting the growth of plants | |
JPH08500367A (en) | Potato germination inhibitor | |
JP2010514762A (en) | Herbicidal composition and method for inhibiting weed growth | |
JPS637521B2 (en) | ||
JPH025722B2 (en) | ||
US7396801B1 (en) | Moss control composition | |
CA3143857A1 (en) | Stable herbicidal compositions comprising amine oxide and betaine | |
JP3338723B2 (en) | Apple flower remover | |
JP2006076920A (en) | Moss controlling agent for turf | |
JP2004277346A (en) | Composition for suppressing differentiation of flower bud of japanese cedar and/or white cedar | |
CN114617132B (en) | Weeding composition, herbicide and preparation method | |
ES2280044T5 (en) | USE OF ACILCICLOHEXANODIONA DERIVATIVES TOGETHER WITH ETEFONA TO TREAT POMÁCEAS FRUITS. | |
JP2007230885A (en) | Method for preventing turf from summer decline and summer decline-proofing agent for turf | |
KR100197302B1 (en) | Herbicidal agent comprising n-phenyl-3,4,5,6-tetrahydrophthalimide and a derivative of phenoxyalkancarboxylic acid | |
JP4094227B2 (en) | Flowering agent for apple trees | |
JP3405764B2 (en) | Antagonistic inhibitor for herbicide, herbicide composition and herbicidal method | |
WO2024105181A1 (en) | Maleic hydrazide formulations | |
JPH07187915A (en) | Herbicidal composition for direct application to water surface and herbicidal method | |
JPH0330563B2 (en) |