JPS6138164B2 - - Google Patents
Info
- Publication number
- JPS6138164B2 JPS6138164B2 JP53136275A JP13627578A JPS6138164B2 JP S6138164 B2 JPS6138164 B2 JP S6138164B2 JP 53136275 A JP53136275 A JP 53136275A JP 13627578 A JP13627578 A JP 13627578A JP S6138164 B2 JPS6138164 B2 JP S6138164B2
- Authority
- JP
- Japan
- Prior art keywords
- antibiotics
- phytotoxicity
- plants
- drug
- symptoms
- 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
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- 241001454295 Tetranychidae Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
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- 239000008186 active pharmaceutical agent Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 150000003797 alkaloid derivatives Chemical class 0.000 description 1
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- 239000003443 antiviral agent Substances 0.000 description 1
- 230000003935 attention Effects 0.000 description 1
- 239000005667 attractant Substances 0.000 description 1
- 244000000005 bacterial plant pathogen Species 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
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- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
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- 229960005091 chloramphenicol Drugs 0.000 description 1
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- 235000007240 daidzein Nutrition 0.000 description 1
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- 201000010099 disease Diseases 0.000 description 1
- YDEXUEFDPVHGHE-GGMCWBHBSA-L disodium;(2r)-3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Na+].[Na+].COC1=CC=CC(C[C@H](CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O YDEXUEFDPVHGHE-GGMCWBHBSA-L 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 229940088679 drug related substance Drugs 0.000 description 1
- 244000013123 dwarf bean Species 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
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- 235000019441 ethanol Nutrition 0.000 description 1
- 150000002213 flavones Chemical class 0.000 description 1
- RIKPNWPEMPODJD-UHFFFAOYSA-N formononetin Natural products C1=CC(OC)=CC=C1C1=COC2=CC=CC=C2C1=O RIKPNWPEMPODJD-UHFFFAOYSA-N 0.000 description 1
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- 235000010209 hesperetin Nutrition 0.000 description 1
- 229960001587 hesperetin Drugs 0.000 description 1
- FTODBIPDTXRIGS-UHFFFAOYSA-N homoeriodictyol Natural products C1=C(O)C(OC)=CC(C2OC3=CC(O)=CC(O)=C3C(=O)C2)=C1 FTODBIPDTXRIGS-UHFFFAOYSA-N 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 238000011835 investigation Methods 0.000 description 1
- 235000008800 isorhamnetin Nutrition 0.000 description 1
- IZQSVPBOUDKVDZ-UHFFFAOYSA-N isorhamnetin Chemical compound C1=C(O)C(OC)=CC(C2=C(C(=O)C3=C(O)C=C(O)C=C3O2)O)=C1 IZQSVPBOUDKVDZ-UHFFFAOYSA-N 0.000 description 1
- 235000008777 kaempferol Nutrition 0.000 description 1
- 235000021332 kidney beans Nutrition 0.000 description 1
- LRDGATPGVJTWLJ-UHFFFAOYSA-N luteolin Natural products OC1=CC(O)=CC(C=2OC3=CC(O)=CC(O)=C3C(=O)C=2)=C1 LRDGATPGVJTWLJ-UHFFFAOYSA-N 0.000 description 1
- 235000009498 luteolin Nutrition 0.000 description 1
- IQPNAANSBPBGFQ-UHFFFAOYSA-N luteolin Chemical compound C=1C(O)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(O)C(O)=C1 IQPNAANSBPBGFQ-UHFFFAOYSA-N 0.000 description 1
- 230000036244 malformation Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
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- 235000007708 morin Nutrition 0.000 description 1
- PCOBUQBNVYZTBU-UHFFFAOYSA-N myricetin Natural products OC1=C(O)C(O)=CC(C=2OC3=CC(O)=C(O)C(O)=C3C(=O)C=2)=C1 PCOBUQBNVYZTBU-UHFFFAOYSA-N 0.000 description 1
- 235000007743 myricetin Nutrition 0.000 description 1
- 229940116852 myricetin Drugs 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- WGEYAGZBLYNDFV-UHFFFAOYSA-N naringenin Natural products C1(=O)C2=C(O)C=C(O)C=C2OC(C1)C1=CC=C(CC1)O WGEYAGZBLYNDFV-UHFFFAOYSA-N 0.000 description 1
- 235000007625 naringenin Nutrition 0.000 description 1
- 229940117954 naringenin Drugs 0.000 description 1
- 229930019673 naringin Natural products 0.000 description 1
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- 229940052490 naringin Drugs 0.000 description 1
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- 230000000361 pesticidal effect Effects 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- SUYJZKRQHBQNCA-UHFFFAOYSA-N pinobanksin Natural products O1C2=CC(O)=CC(O)=C2C(=O)C(O)C1C1=CC=CC=C1 SUYJZKRQHBQNCA-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- 235000013824 polyphenols Nutrition 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- FDRQPMVGJOQVTL-UHFFFAOYSA-N quercetin rutinoside Natural products OC1C(O)C(O)C(CO)OC1OCC1C(O)C(O)C(O)C(OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 FDRQPMVGJOQVTL-UHFFFAOYSA-N 0.000 description 1
- 230000001603 reducing effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- JGUZGNYPMHHYRK-UHFFFAOYSA-N rhamnetin Chemical compound C=1C(OC)=CC(O)=C(C(C=2O)=O)C=1OC=2C1=CC=C(O)C(O)=C1 JGUZGNYPMHHYRK-UHFFFAOYSA-N 0.000 description 1
- ALABRVAAKCSLSC-UHFFFAOYSA-N rutin Natural products CC1OC(OCC2OC(O)C(O)C(O)C2O)C(O)C(O)C1OC3=C(Oc4cc(O)cc(O)c4C3=O)c5ccc(O)c(O)c5 ALABRVAAKCSLSC-UHFFFAOYSA-N 0.000 description 1
- IKGXIBQEEMLURG-BKUODXTLSA-N rutin Chemical compound O[C@H]1[C@H](O)[C@@H](O)[C@H](C)O[C@@H]1OC[C@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](OC=2C(C3=C(O)C=C(O)C=C3OC=2C=2C=C(O)C(O)=CC=2)=O)O1 IKGXIBQEEMLURG-BKUODXTLSA-N 0.000 description 1
- 235000005493 rutin Nutrition 0.000 description 1
- 229960004555 rutoside Drugs 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003892 spreading Methods 0.000 description 1
- 239000006273 synthetic pesticide Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229940063650 terramycin Drugs 0.000 description 1
- IDELNEDBPWKHGK-UHFFFAOYSA-N thiobutabarbital Chemical compound CCC(C)C1(CC)C(=O)NC(=S)NC1=O IDELNEDBPWKHGK-UHFFFAOYSA-N 0.000 description 1
- DFQMKYUSAALDDY-MQEBUAKTSA-N trinactin Chemical compound C[C@@H]([C@@H]1CC[C@@H](O1)C[C@H](OC(=O)[C@H](C)[C@H]1CC[C@H](O1)C[C@H](CC)OC(=O)[C@@H](C)[C@@H]1CC[C@@H](O1)C[C@@H](CC)OC(=O)[C@@H]1C)CC)C(=O)O[C@@H](C)C[C@@H]2CC[C@H]1O2 DFQMKYUSAALDDY-MQEBUAKTSA-N 0.000 description 1
- DFQMKYUSAALDDY-UHFFFAOYSA-N trinactin Natural products CC1C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(CC)CC(O2)CCC2C(C)C(=O)OC(C)CC2CCC1O2 DFQMKYUSAALDDY-UHFFFAOYSA-N 0.000 description 1
- 239000000273 veterinary drug Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
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- 239000004563 wettable powder Substances 0.000 description 1
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A50/00—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
- Y02A50/30—Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
本発明は、植物の薬害防止剤に係わるものであ
る。更に詳しくは、抗生物質を植物に施用するに
あたり、フラボノイド類、レセルピンあるいはカ
ロチンの1種または2種以上を抗生物質の施用
前、施用と同時にあるいは施用後に散布すること
によつて、抗生物質によつて発生する薬害を著し
く低減化、もしくは薬害の発生を完全に防止し植
物の成育を良好にする薬害防止剤である。
抗生物質剤は農薬として古くから用いられてい
た。例えば、医薬あるいは動物薬として開発され
たストレプトマイシン、クロラムフエニコール、
オキシテトラサイクリン、グリセオフルビン等が
植物寄生性細菌類の防除用薬剤として農薬分野へ
応用開発された。また、当初から農薬として開発
されたものとしてシクロヘキシミド、プラストサ
イジンS、カスガマイシン、ポリオキシン、ノボ
ビオシン、マクロテトロライド系(イナクチン、
モナクチン、ジナクチン、トリナクチン、テトラ
ナクチン等)、エゾマイシン等があげられる。こ
れら殺菌性と殺虫殺ダニ性を示す抗生物質剤の登
場以来、その安定した効果に着目され現在では大
量に使用されるようになつた。
これらの抗生物質剤は、一般的に選択性が高
く、対象病害虫類に対して抵抗性の発達がほとん
どないため単位面積当りの施用薬量が少なく、そ
の上原体に薬臭がないため使用時における薬臭と
収穫物に対する残臭がなく、しかも作物および土
壌残留も短い等多くの点で合成農薬より有利であ
る。
しかし、これらの抗生物質剤の欠点としては、
植物に施用した場合、各種の植物に対してクロロ
シス症状あるいは奇形症状のような生理障害を起
こすことがある。このような生理障害作用を与え
たりする抗生物質は、当然農作物の減収あるいは
収穫物の品質低下を起こしたり、また植物を枯死
させたりする。したがつて、植物に対し、しばし
ば生理障害を与える抗生物質は使用場面で制約を
受けたり、場合によつては防除用薬剤として使用
されないことがある。例えば、多くの植物病原性
細菌類に有効であるシクロヘキシミドは低濃度の
使用でも強い薬害が発生するため、薬剤の適用範
囲はカラマツとネギ類に限定され、施用濃度も低
濃度に制約されている。また、ブラストサイジン
S剤の場合は、ベンジルアミノベンゼンスルホン
酸塩との混合製剤によりイネを対象とした殺菌剤
が実用化されているが、この薬剤もイネに対し施
用濃度が高かつたり、あるいは施用回数が多かつ
た場合は黄白色の薬害を発生させる。また、イネ
以外の作物であるナス科作物を始めとする多くの
植物に対しても薬害を発生させることは周知であ
る。以上のほか、ストレプトマイシン、カスガマ
イシン、アグリマイシン(有効成分としてオキシ
テトラサイクリンとストレプレマイシンの混合製
剤)などの抗生物質でも植物の種類とか施用時期
あるいは施用回数などによつて薬害を発生させる
ことは報告されている。
以上述べたように、多くの抗生物質が植物に対
して薬害を発生させることは周知であるが、その
薬害を軽減させたり、あるいは完全に防止する薬
剤は極めて少なく、次の2例が報告されているだ
けである。
例1 キユウリとインゲンに薬害を発生させた抗
生物質のオーレオマイシン、ストレプトマイシ
ン、テラマイシンに対して1%のクロロフイリ
ンを添加することにより薬害を減少させた。
(Plant Disease Reporter Vol.42No.11 1203〜
1205頁 1958年)
例2 ブラストサイジンSにベンジルアミノベン
ゼンスルホン酸塩を加え塩とした製剤をイネに
対して施すことにより薬斑軽減効果を示した。
(農薬生産技術24〜29頁 1963年、化学と生物
Vol.2No.5 272〜276頁 1962年)
しかしながら、例1の場合はクロロフイリンの
量を多量に使用しなければ軽減効果を示さず実用
化はされていない。
本発明者らは、植物に対して薬害を発生させる
抗生物質の薬害防止剤あるいは薬害軽減剤の開発
を目的として長期にわたり研究を重ねたところ、
抗生物質とフラボノイド類、アルカロイド類ある
いはカロチノイド類から選ばれた化合物の1種ま
たは2種以上を抗生物質の施用前、施用と同時あ
るいは施用後に散布することによつて抗生物質の
持つている殺菌性、殺虫殺ダニ性などの特性に何
んら変化を与えることなく薬害を防止することを
見出し本発明を完成した。
本発明で用いられる薬害防止剤としては次のよ
うなものが挙げられる。フラボノイド類として
は、例えばカリコプテリン(Calycopterin)、ク
リシン(Chrysin)フラボン(Flavone)、ガラン
ギン(Galangin)、ゲンカニン(Genkwanin)、
ゴツシペチン(Gossypeti)、イソラムネチン
(Isorhamnetin)、ケンフエロール
(Kaempferol)ルテオリン(Luteolin)、モリン
(Morin)、ミリセチン(Myricetin)、プリムレチ
ン(Primuletin)、ルチン(Rutin)、ラムネチン
(Rhamnetin)、トリシン(Toricin)、ビオカニン
A(Biochanin)、ダイゼイン(Daidzein)ホルム
オノネチン(Formononetin)、ゲニスチン
(Genistin)、サンタール(Santal)、ブチン
(Butin)、カテキン(Catechin)、エリオジクチオ
ール(Eriodictyol)、ヘスペレチン
(Hesperetin)、ナリンギン(Naringenin)等が
挙げられ、またアルカロイド類のレセルピン
(Reserpine)並びにカロチノイド類のα―,β
―,γ―位カロチン(Carotine)が挙げられる。
本発明の薬害防止剤は、単体または各種の担体
と混合して粉剤、水和剤、乳剤、水溶液などの剤
型で使用することができる。各種の担体として
は、例えばホワイトカーボン、ケイソウ土、タル
ク、合成アルミナ、フエノール酢酸、クレー、n
―ヘキサン、シクロヘキサン、ベンゼン、キシロ
ール、エチルアルコール、アセトン、水等を挙げ
ることができる。また必要に応じて展着剤、乳化
剤、分散剤、協力剤等の補助剤と、あるいは殺虫
剤、殺ダニ剤、殺菌剤、抗ウイルス剤、植物生長
調節剤、誘引剤等と混合して用いることもでき
る。
次に実施例を挙げて説明する。
実施例 1
レセルピン 20重量部
イソプロピルアルコール 30 〃
キシロール 40 〃
ポリオキシエチレンノニルフエニル
エーテルとアルキルベンゼンスルホ
ン酸カルシウム(1:1の混合物) 10 〃
これらの各成分をよく混合して乳剤とする。
実施例 2
フラボン 40 重量部
リグニンスルホン酸ナトリウム 4.5 〃
ホワイトカーボン 3 〃
クレー 52.5 〃
これらの各成分をよく混合して粉砕して水和剤
として用いる。
実施例 3
β―カロチン 10 重量部
ナリンギン 10 〃
ドデシルベンゼンスルホン酸
ナトリウム 1.5 〃
ケイソウ土 38 〃
ベントナイト 40.5 〃
これらの各成分を混合して粉剤として用いる。
以下、試験例を挙げて本発明の効果を明らかに
する。いずれの試験においても抗生物質によつて
生じるクロロシス症状と奇形症状の程度をそれぞ
れ5段階に区分けし以下の薬害判定基準とした。
判定基準
クロロシス症状の場合
0……全く発生しなかつたもの
1……僅かに発生したもの
2……葉の1/4程度に発生したもの
3……葉の半分程度に発生したもの
4……葉の3/4程度に発生したもの
5……全体に発生したもの
奇形症状の場合
0……全く発生しなかつたもの
1……僅かに変形したもの
2……萎凋と裂片の発現が僅かに認められたも
の
3……萎凋と裂片の発現が強く認められたもの
4……萎凋と裂片の発現が強く、その上カツプ
ル状の症状を僅かに呈しているもの
5……カツプ状になつたもの
試験例 1
径7cmの素焼鉢にそ菜類培養土壌(クレハ化学
社製)100gを入れ、キユウリ(品種・松風)種
子を播種し、温室内で第1本葉が2〜2.5cm程度
に生育させた苗に各抗生物質と本薬剤を所定濃度
とした水溶液を十分散布処理した。処理した苗を
7日間温室内にて育成させたのち、薬害の発生程
度、草丈および生体重量を調査した。その結果を
第1表に示す。
The present invention relates to an agent for preventing phytotoxicity of plants. More specifically, when applying antibiotics to plants, one or more of flavonoids, reserpine, or carotene can be applied before, at the same time, or after the application of the antibiotic. It is a phytotoxicity preventive agent that significantly reduces or completely prevents phytotoxicity that occurs due to phytotoxicity, and improves the growth of plants. Antibiotics have long been used as pesticides. For example, streptomycin, chloramphenicol, which was developed as a pharmaceutical or veterinary drug,
Oxytetracycline, griseofulvin, etc. have been developed in the field of agrochemicals as agents for controlling plant-parasitic bacteria. In addition, cycloheximide, plasticidin S, kasugamycin, polyoxin, novobiocin, macrotetrolides (inactin,
Monactin, dinactin, trinactin, tetranactin, etc.), ezomycin, etc. Since the advent of these antibiotics that exhibit bactericidal and insecticidal and acaricidal properties, attention has been paid to their stable effects, and they have now come to be used in large quantities. These antibiotics generally have high selectivity and hardly develop resistance to the target pests, so the amount of application per unit area is small, and in addition, the drug substance does not have a medicinal odor, so it is difficult to use. It is advantageous over synthetic pesticides in many respects, such as no medicinal odor or residual odor on crops, and short residues on crops and soil. However, the disadvantages of these antibiotics are that
When applied to plants, it may cause physiological disorders such as chlorosis symptoms or malformation symptoms in various plants. Antibiotics that cause such physiological disturbances naturally cause a decrease in the yield of agricultural crops, a decline in the quality of the crops, and even cause the plants to wither. Therefore, antibiotics that often cause physiological disorders to plants are subject to restrictions in their use, and in some cases may not be used as pesticidal agents. For example, cycloheximide, which is effective against many plant pathogenic bacteria, causes strong phytotoxicity even when used at low concentrations, so the range of application of the drug is limited to larch and alliums, and the application concentration is also restricted to low concentrations. . In addition, in the case of Blasticidin S agent, a fungicide targeted at rice has been put into practical use by combining it with benzylaminobenzenesulfonate, but this agent also has a high concentration of application to rice. Or, if applied too many times, yellowish-white chemical damage will occur. Furthermore, it is well known that it causes phytotoxicity to many plants including crops of the Solanaceae family, which are crops other than rice. In addition to the above, antibiotics such as streptomycin, kasugamycin, and agrimycin (a mixed preparation of oxytetracycline and strepremycin as active ingredients) have not been reported to cause chemical damage depending on the type of plant, the timing of application, or the number of applications. ing. As mentioned above, it is well known that many antibiotics cause phytotoxicity to plants, but there are very few drugs that can reduce or completely prevent such phytotoxicity, and the following two cases have been reported. It's just that. Example 1 Addition of 1% chlorophyllin to the antibiotics aureomycin, streptomycin, and terramycin, which caused chemical damage to cucumbers and kidney beans, reduced the chemical damage.
(Plant Disease Reporter Vol.42No.11 1203~
(1205 pages, 1958) Example 2 A drug spot reducing effect was demonstrated by applying a salt preparation of Blasticidin S with benzylaminobenzene sulfonate to rice.
(Pesticide Production Technology pp. 24-29, 1963, Chemistry and Biology
(Vol. 2 No. 5, pp. 272-276, 1962) However, in the case of Example 1, the reduction effect is not shown unless a large amount of chlorophyllin is used, and it has not been put to practical use. The present inventors have conducted extensive research over a long period of time with the aim of developing an agent to prevent or reduce the phytotoxicity of antibiotics that cause phytotoxicity to plants.
The bactericidal properties of antibiotics can be improved by spraying antibiotics and one or more compounds selected from flavonoids, alkaloids, or carotenoids before, simultaneously with, or after the application of antibiotics. The present invention was completed by discovering that chemical damage can be prevented without any change in properties such as insecticidal and acaricidal properties. Examples of the chemical damage preventive agent used in the present invention include the following. Examples of flavonoids include Calycopterin, Chrysin, Flavone, Galangin, Genkwanin,
Gossypeti, Isorhamnetin, Kaempferol, Luteolin, Morin, Myricetin, Primuletin, Rutin, Rhamnetin, Toricin, Biochanin A (Biochanin), Daidzein, Formononetin, Genistin, Santal, Butin, Catechin, Eriodictyol, Hesperetin, Naringenin In addition, the alkaloid reserpine and the carotenoids α- and β
-, γ-position carotene (Carotine) is mentioned. The chemical damage inhibitor of the present invention can be used alone or mixed with various carriers in the form of powders, wettable powders, emulsions, aqueous solutions, and the like. Examples of various carriers include white carbon, diatomaceous earth, talc, synthetic alumina, phenolic acetic acid, clay, n
-Hexane, cyclohexane, benzene, xylol, ethyl alcohol, acetone, water, etc. Also, if necessary, it may be mixed with adjuvants such as spreading agents, emulsifiers, dispersants, synergists, etc., or with insecticides, acaricides, fungicides, antiviral agents, plant growth regulators, attractants, etc. You can also do that. Next, an example will be given and explained. Example 1 Reserpine 20 parts by weight Isopropyl alcohol 30 Xylol 40 Polyoxyethylene nonyl phenyl ether and calcium alkylbenzenesulfonate (1:1 mixture) 10 These components are thoroughly mixed to form an emulsion. Example 2 Flavone 40 parts by weight Sodium ligninsulfonate 4.5 White carbon 3 Clay 52.5 These components are thoroughly mixed and pulverized to be used as a wettable powder. Example 3 β-carotene 10 parts by weight Naringin 10 Sodium dodecylbenzenesulfonate 1.5 Diatomaceous earth 38 Bentonite 40.5 These components are mixed and used as a powder. Hereinafter, the effects of the present invention will be clarified by giving test examples. In both tests, the severity of chlorotic symptoms and deformity symptoms caused by antibiotics was divided into five levels, and the following criteria for drug damage were used. Judgment criteria For chlorosis symptoms: 0... Not occurring at all 1... Slight occurrence 2... Appearing on about 1/4 of the leaves 3... Appearing on about half of the leaves 4... 5: Occurred on about 3/4 of the leaf 5: Occurred all over the leaf 0: Abnormal symptoms: 0: No occurrence at all 1: Slightly deformed 2: Slight wilting and lobes Observed: 3: Severe signs of wilting and lobes 4: Severe signs of wilting and lobes, with slight cup-like symptoms 5: Cup-like symptoms Product test example 1 Put 100 g of rapeseed culture soil (manufactured by Kureha Chemical Co., Ltd.) into a clay pot with a diameter of 7 cm, sow cucumber (variety: Matsukaze) seeds, and grow the first true leaves to about 2 to 2.5 cm in a greenhouse. The seedlings were thoroughly sprayed with an aqueous solution containing each antibiotic and this drug at a specified concentration. After growing the treated seedlings in a greenhouse for 7 days, the degree of chemical damage, plant height, and live weight were investigated. The results are shown in Table 1.
【表】【table】
【表】【table】
【表】
試験例 2
3〜4葉期に育成させたナス苗に対して各抗生
物質と本薬剤を含有させた水溶液を十分に散布処
理し、散布7日後における薬害発生程度を調査し
た。その結果を第2表に示す。[Table] Test Example 2 Eggplant seedlings grown at the 3rd to 4th leaf stage were thoroughly sprayed with an aqueous solution containing each antibiotic and this drug, and the degree of phytotoxicity was investigated 7 days after the spraying. The results are shown in Table 2.
【表】【table】
【表】
試験例 3
イネ苗(3〜4葉期)を1/5000アールのワグネ
ルポツトに4本定植し、定植後7日目に抗生物質
と本薬剤をそれぞれ処理した。薬害発生の調査は
処理15日後に行なつた。その結果を第3表に示
す。[Table] Test Example 3 Four rice seedlings (3-4 leaf stage) were planted in 1/5000 are Wagner pots, and 7 days after planting, they were treated with antibiotics and this drug, respectively. Investigation of the occurrence of drug damage was carried out 15 days after treatment. The results are shown in Table 3.
【表】【table】
【表】
試験例 4
径7cmの素焼鉢に4葉期のイネ苗を10本植え、
これに抗生物質と本製剤を散布処理した。処理1
日後に温室内でイネに継続的に接種を行なつて得
られたイモチ症菌胞子を顕微鏡1視野(15×10
倍)30個の胞子を含むように調整した液を1鉢当
り5mlの割合で散布した。散布後ビニール製の湿
室内(湿度100%、温度25℃)に置き、24時間後
に温室に移し、高温に保ち散布7日目に病斑数を
数え下記の方法で防除価を算出した。その結果を
第4表に示す。
防除価(%)
=無処理区の病斑数−処理区の病斑数/無処理区の病
斑数×100[Table] Test example 4 Ten rice seedlings at the four-leaf stage were planted in clay pots with a diameter of 7 cm.
This was sprayed with antibiotics and this preparation. Processing 1
After 1 day, rice was continuously inoculated in a greenhouse, and the spores of the potato fungus obtained were examined in one field of view (15 x 10
A solution adjusted to contain 30 spores was sprayed at a rate of 5 ml per pot. After spraying, the plants were placed in a vinyl humidity chamber (humidity 100%, temperature 25°C), and 24 hours later they were transferred to a greenhouse, kept at a high temperature, and on the seventh day of spraying, the number of lesions was counted and the control value was calculated using the method below. The results are shown in Table 4. Control value (%) = Number of lesions in untreated area - Number of lesions in treated area / Number of lesions in untreated area x 100
【表】【table】
【表】
試験例 5
径5cmの鉢に育成したインゲンにニセナミハダ
ニ雌成虫を1鉢当り150匹接種し、抗生物質のイ
ナクチン、モナクチンあるいはノナクチンとモナ
クチン混合物に対し、本薬剤のモリン、ルチン、
レセルピン、β―カロチンおよびフラボンを同一
量配合し、この配合物を120,60,30,15および
7.5ppmになるように希釈した水溶液を散布し、
散布24時間後における殺ダニ効果を調査した。そ
の結果、殺ダニ率はすべて100%の効果を示し、
本薬剤を混合しても殺ダニ力価の低下は認められ
ないことが判明した。[Table] Test Example 5 Green beans grown in pots with a diameter of 5 cm were inoculated with 150 female adult spider mites per pot.
The same amounts of reserpine, β-carotene and flavones were added, and this mixture was mixed with 120, 60, 30, 15 and
Spray an aqueous solution diluted to 7.5ppm,
The acaricidal effect was investigated 24 hours after spraying. As a result, the mite killing rate was 100% effective.
It was found that no decrease in acaricidal titer was observed even when this drug was mixed.
Claims (1)
イド類、レセルピンあるいはカロチンの1種また
は2種以上を有効成分として含有することを特徴
とする薬害防止剤。1. An agent for preventing plant damage caused by antibiotics, which contains one or more of flavonoids, reserpine, or carotene as an active ingredient.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13627578A JPS5564508A (en) | 1978-11-07 | 1978-11-07 | Preventive from damage by agricultural chemicals |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP13627578A JPS5564508A (en) | 1978-11-07 | 1978-11-07 | Preventive from damage by agricultural chemicals |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5564508A JPS5564508A (en) | 1980-05-15 |
JPS6138164B2 true JPS6138164B2 (en) | 1986-08-28 |
Family
ID=15171376
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP13627578A Granted JPS5564508A (en) | 1978-11-07 | 1978-11-07 | Preventive from damage by agricultural chemicals |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5564508A (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5141745A (en) * | 1986-03-27 | 1992-08-25 | The Lubrizol Corporation | Nodulation inducing factors |
ZA872087B (en) * | 1986-03-27 | 1988-06-29 | Lubrizol Genetics Inc | Nodulation inducing factors |
EP0263553A3 (en) * | 1986-09-30 | 1989-03-08 | Shell Internationale Researchmaatschappij B.V. | Method of inhibiting gene induction |
KR101002570B1 (en) | 2008-07-08 | 2010-12-20 | 아이엠팜(주) | A composition of beta carotene for functional apple growing |
CN102627623B (en) * | 2012-03-20 | 2014-07-02 | 中国科学院新疆理化技术研究所 | Method for preparing butin from Vernonia anthelmintica fruits |
CN109221263B (en) * | 2018-10-30 | 2021-03-02 | 湖南人文科技学院 | Botanical herbicide safener and method for relieving rice phytotoxicity |
-
1978
- 1978-11-07 JP JP13627578A patent/JPS5564508A/en active Granted
Also Published As
Publication number | Publication date |
---|---|
JPS5564508A (en) | 1980-05-15 |
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