JPH092911A - Bacterial wilt controlling agent - Google Patents
Bacterial wilt controlling agentInfo
- Publication number
- JPH092911A JPH092911A JP7178106A JP17810695A JPH092911A JP H092911 A JPH092911 A JP H092911A JP 7178106 A JP7178106 A JP 7178106A JP 17810695 A JP17810695 A JP 17810695A JP H092911 A JPH092911 A JP H092911A
- Authority
- JP
- Japan
- Prior art keywords
- bacterial wilt
- bacillus subtilis
- bacillus cereus
- soil
- bacillus
- 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
Links
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明はカニ殻とバチラス・セレ
ウス(Bacillus cereus) 及び/又はバチラス・ズブチリ
ス(Bacillus subtilis) との混合物からなる青枯病防除
材に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a bacterial wilt control material comprising a mixture of a crab shell and Bacillus cereus and / or Bacillus subtilis.
【0002】[0002]
【従来の技術】ナス科作物は連作することでしばしば青
枯病にかかり、農家に多大な損失を与えている。2. Description of the Related Art Cropping of solanaceous crops often causes bacterial wilt by continuous cropping, which causes a great loss to farmers.
【0003】青枯病の防除方法としてはいくつかの方法
が試みられている。例えば、その方法としてクロルピク
リンや臭化メチルなどの薬剤による土壌殺菌があげられ
る。しかし、これら薬剤による土壌殺菌は、有益な菌や
ミミズ等の有益な土壌動物まで無差別に殺し、土壌微生
物の構成を崩し殺菌後の外部からの持ち込みによる病害
の激発を誘発する危険性がある。有益な菌や土壌動物等
の減少は作物の健全な生育を阻害する。また、これら薬
剤は刺激臭があり、コスト高であるばかりでなく、オゾ
ン層の破壊、繰り返し施用による土壌残留汚染等環境問
題を引き起こしている。[0003] Several methods have been tried as a method for controlling bacterial wilt. For example, the method includes soil sterilization with a drug such as chlorpicrin or methyl bromide. However, soil sterilization with these agents may indiscriminately kill beneficial soil animals such as beneficial bacteria and earthworms, destroying the composition of soil microorganisms and inducing a disease outbreak caused by bringing in from outside after sterilization. . The reduction of beneficial fungi and soil animals inhibits the healthy growth of crops. In addition, these agents have an irritating odor and are not only costly, but also cause environmental problems such as ozone layer destruction and soil residual contamination due to repeated application.
【0004】他の防除方法としては、青枯病菌であるシ
ュウドモナス・ソラナシラム(Pseudomonas solanacearu
m)の拮抗菌を増殖させるために畜産糞、おがくず、稲藁
等から調製した堆肥を施用する方法や、青枯病に対する
耐病性を高めるために、病害に強い苗に接ぎ木をする方
法も行われている。しかし堆肥の施用は一定した効果が
期待できず、接ぎ木においても、現状ではナス科植物の
青枯病に関しては十分効果的な台木は開発されてない。
また、微生物を利用して連作障害を抑制、防除する方法
もいくつか報告されている。[0004] As another control method, Pseudomonas solanacearu, a bacterial wilt fungus, is used.
m) The method of applying compost prepared from livestock dung, sawdust, rice straw, etc. to grow the antagonistic bacteria, and the method of grafting seedlings resistant to disease to increase disease resistance against wilt disease are also available. It is being appreciated. However, the application of compost cannot be expected to have a certain effect, and even in grafting, at present, a rootstock that is not sufficiently effective for the bacterial wilt of Solanaceae has not been developed.
In addition, several methods have been reported for controlling and controlling continuous cropping disorders using microorganisms.
【0005】例えば特開昭61-200193 号公報には各種の
微生物の生菌体または胞子を使用した根圏土壌改良剤が
開示され、微生物の生育促進資材としてカニ殻が例示さ
れているが、後述する本発明を開示するものではない。
更に日本植物病理学会報Vol.58(1992)には正田等がバチ
ラス・ズブチリスを用いてトマト根腐れ萎凋病、青枯病
を防除する方法を報告している。しかし、一般に拮抗菌
を利用した場合土壌中での生存率が低いことや、失活等
により充分な効果が得られていないため実用化には至っ
ていない。For example, JP-A-61-200193 discloses a rhizosphere soil improving agent using living cells or spores of various microorganisms, and crab shells are exemplified as a material for promoting the growth of microorganisms. It does not disclose the present invention described below.
Furthermore, in the Japan Society for Plant Pathology Vol.58 (1992), Masada et al. Reported a method for controlling tomato root rot wilt disease and bacterial wilt disease using Bacillus subtilis. However, in general, when an antagonistic bacterium is used, the survival rate in soil is low, and a sufficient effect is not obtained due to deactivation and the like, so that it has not been put into practical use.
【0006】[0006]
【発明が解決しようとする課題】本発明はかかる現状に
鑑みなされたものであって、本発明の目的は青枯病に対
して抑制効果が高く、低コストで繰り返して施用しても
環境に影響のない青枯病防除材を提供することにある。
我々は既にシュウドモナス・フルオレッセンス(Pseudom
onas fluorescens) とカニ殻を混合する資材を提案し
た。しかし更に鋭意検討を進めた結果シュウドモナス・
フルオレッセンスに代わりバチラス・セレウス及び/又
はバチラス・ズブチリスを用いればより効果的であるこ
とを見い出し本発明を完成した。SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and an object of the present invention is to have a high inhibitory effect against bacterial wilt disease and to be environmentally friendly even when repeatedly applied at low cost. An object is to provide a wilt control agent which has no influence.
We already have Pseudomonas fluorescens (Pseudom
I proposed a material to mix onas fluorescens) and crab shells. However, as a result of further diligent examination, Pseudomonas
The present invention has been completed by finding that it is more effective to use Bacillus cereus and / or Bacillus subtilis instead of fluorescence.
【0007】[0007]
【課題を解決するための手段】即ち本発明はカニ殻とバ
チラス・セレウス及び/又はバチラス・ズブチリスとの
混合物からなる青枯病防除材に関する。That is, the present invention relates to a bacterial wilt controlling material comprising a mixture of crab shell and Bacillus cereus and / or Bacillus subtilis.
【0008】本発明者らはこのバチラス・セレウス及び
バチラス・ズブチリスの青枯病菌に対する拮抗性をin v
itroで調べた結果、拮抗性が認められたが、これらのバ
チラス・セレウス及びバチラス・ズブチリスの菌体のみ
を青枯病で汚染された土壌に施用しても作物の青枯病を
防除することはできなかった。The inventors of the present invention have shown that the antagonism of Bacillus cereus and Bacillus subtilis to bacterial wilt disease in v
As a result of itro's examination, antagonisticity was recognized, but even if only these Bacillus cereus and Bacillus subtilis cells are applied to soil contaminated with bacterial wilt, the bacterial wilt of crops can be controlled. I couldn't.
【0009】そこでこのin vitroで認められているバチ
ラス・セレウス及びバチラス・ズブチリスの青枯病に対
する拮抗性を青枯病汚染土壌で発現させる方法について
検討し、本発明を完成したものである。Therefore, the present invention has been completed by studying a method of expressing the antagonistic activity against the bacterial wilt of Bacillus cereus and Bacillus subtilis, which has been observed in vitro, in soil infected with bacterial wilt.
【0010】[0010]
【作用】以下に本発明を詳記する。本発明の青枯病防除
材の製造方法としては、あらかじめカニ殻を5mm 以下、
好ましくは1 〜5mm に砕き、このカニ殻にバチラス・セ
レウス及び/又はバチラス・ズブチリスの培養物を混合
するのが最も安価である。取り扱いを容易にするため混
合後室温から70℃で乾燥しても良い。The present invention will be described below in detail. As a method for producing the bacterial wilt control material of the present invention, a crab shell of 5 mm or less in advance,
It is the cheapest to crush to 1 to 5 mm, and to mix the culture of Bacillus cereus and / or Bacillus subtilis into the crab shell. After mixing, it may be dried at room temperature to 70 ° C. for easy handling.
【0011】バチラス・セレウス及び/又はバチラス・
ズブチリスの培養物は、肉エキス、ペプトン、酵母エキ
ス、澱粉、グルコース、しょ糖、リン酸カリウム、硫酸
マグネシウム等の栄養源を含んだ培地を用い、pHを7 付
近に調整した後温度20〜45℃、好ましくは25〜35℃で、
好気的に約24時間培養することにより製造する。Bacillus cereus and / or Bacillus
The culture of subtilis is a medium containing nutrients such as meat extract, peptone, yeast extract, starch, glucose, sucrose, potassium phosphate, magnesium sulfate, etc., and after adjusting the pH to around 7, the temperature is 20-45 ° C. Preferably at 25-35 ° C,
It is produced by aerobically culturing for about 24 hours.
【0012】本発明防除材はバチラス・セレウス及び/
又はバチラス・ズブチリスとカニ殻との混合物の菌濃度
が104CFU/g以上であることが効果発現の点から好まし
い。The control material of the present invention is Bacillus cereus and / or
Alternatively, the bacterial concentration of the mixture of Bacillus subtilis and crab shell is preferably 10 4 CFU / g or more from the viewpoint of effect expression.
【0013】本発明防除材の製造に際し、炭素源、窒素
源、リン酸カリウム等の栄養源を加えることが出来るこ
とは勿論、ピートモス、バーミキュライト等の微生物着
生材兼土壌改良材を加えることは取り扱いあるいは効果
の点で更に好ましい。In the production of the control material of the present invention, it is of course possible to add a carbon source, a nitrogen source, a nutrient source such as potassium phosphate and the like, and it is not possible to add a microbial growth material and soil improving material such as peat moss and vermiculite. It is more preferable in terms of handling and effect.
【0014】このようにして調製した本発明防除材の使
用方法としては、効果発現の点で作物定植前に土壌に施
用することが望ましい。施用量は防除材の菌濃度により
異なるが一般的には100Kg/10a 以上が好ましい。また、
別法として青枯病初期の作物に施用することもできるが
効果は作物定植前の施用に比べて劣る。As a method of using the pesticidal material of the present invention thus prepared, it is desirable to apply it to soil before planting a plant from the viewpoint of manifesting effects. The application rate varies depending on the bacterial concentration of the control material, but generally 100 Kg / 10a or more is preferable. Also,
Alternatively, it can be applied to crops in the early stage of bacterial wilt, but the effect is inferior to that before planting.
【0015】本発明防除材は拮抗性細菌及びカニ殻とい
う天然物を主材として使用する物であるため、堆肥ある
いは肥料と全く同様に取り扱うことができ、繰り返し施
用しても農薬等のような土壌汚染もなく人畜に対する有
害作用もない。Since the control material of the present invention mainly uses natural materials such as antagonistic bacteria and crab shells, it can be handled in the same manner as compost or fertilizer, and even if it is repeatedly applied, it can be used as a pesticide. There is no soil pollution and no harmful effects on humans and animals.
【0016】[0016]
【実施例】以下に本発明を実施例により更に説明する
が、本発明はこれらに限定されるものではない。また、
%は特に断らない限り全て重量%を示す。EXAMPLES The present invention will be further described below with reference to examples, but the present invention is not limited to these examples. Also,
All percentages are by weight unless otherwise specified.
【0017】(使用材料) 青枯病菌--- 青枯病で枯死したトマト茎内から分離し
たトマトに感染すれば青枯病を発病させる能力を持つシ
ュウドモナス・ソラナシラム。 青枯病菌の培養物--- の青枯病菌をPPGB培地
(ジャガイモ200 gからのポテト煎汁液1000mlにペプト
ン5g、グルコ−ス5g、燐酸2ナトリウム12水塩3
g、燐酸一カリウム0.5 g、食塩3gを溶かしたもの)
で常法により培養したもの。 青枯病菌汚染土壌--- 風乾した加古川沖積土壌にを
添加混合し、水分20%になるよう滅菌水を添加したも
の。 カニ殻---5mm以下に粉砕したもの。 本発明防除材1--- バチラス・セレウス IFO-3003 を
肉エキス培地(肉エキス10g、ペプトン10g、酵母エキ
ス2 g、食塩2 gを水に溶かし1000mlにしたもの)で常
法により培養し、この培養物を各種割合でカニ殻と混合
したもの。 本発明防除材2--- バチラス・ズブチリスIFO-3009を
肉エキス培地(肉エキス1 0 g、ペプトン10g、酵母エ
キス2 g、食塩2 gを水に溶かし1000mlにしたもの)で
常法により培養し、この培養物を各種割合でカニ殻と混
合したもの。 本発明防除材3--- とを混合したもの。 青枯病菌検出培地(原・小野培地)--- ジャガイモ20
0 gからのポテト煎汁液1000mlに硝酸カルシウム4 水塩
0.5 g、燐酸水素2ナトリウム12水塩2 g、ペプトン5
g、庶糖15g、クリスタルバイオレット5mg 、シクロヘ
キシミド50mg、ポリミキシンB硫酸塩50mg、クロラムフ
ェニコ−ル10mg、塩化2,3,5 トリフェニルテトラゾリウ
ム25mgを溶かした液に寒天18gを加え加熱溶解後冷却固
化したもの。(Materials used) Bacterial wilt disease --- Pseudomonas solanasirum having the ability to cause bacterial wilt when infected with tomato isolated from the stem of tomato that died due to bacterial wilt. Bacterial wilt fungus culture --- The bacterial wilt fungus of ---- is treated with PPGB medium (potato decoction 1000 ml of 200 g of potato, 5 g of peptone, 5 g of glucose, disodium phosphate 12-hydrate 3
g, monopotassium phosphate 0.5 g, salt 3 g)
Cultivated by a conventional method. Soil contaminated with bacterial wilt disease --- Soil mixed with air-dried Kakogawa alluvial soil and mixed with sterilized water to a water content of 20%. Crab shell--crushed to 5 mm or less. The control material of the present invention 1 ---- Bacillus cereus IFO-3003 is cultured by a conventional method in a meat extract medium (meat extract 10 g, peptone 10 g, yeast extract 2 g, salt 2 g dissolved in water to 1000 ml), This culture mixed with crab shells in various proportions. Inventive control material 2 --- Bacillus subtilis IFO-3009 is cultured by a conventional method in a meat extract medium (meat extract 10 g, peptone 10 g, yeast extract 2 g, salt 2 g dissolved in water to 1000 ml). Then, this culture was mixed with crab shells at various ratios. A mixture of the present invention pesticide 3--. Bacterial wilt detection medium (Original / Ono medium) --- Potato 20
Calcium nitrate tetrahydrate in 1000 ml of potato decoction from 0 g
0.5 g, disodium hydrogen phosphate dodecahydrate 2 g, peptone 5
g, sucrose 15 g, crystal violet 5 mg, cycloheximide 50 mg, polymyxin B sulfate 50 mg, chloramphenicol 10 mg, and 2,3,5 triphenyltetrazolium chloride 25 mg.
【0018】(実施例1)の青枯病菌汚染土壌125g
(乾重で100g)を直径158mm の大型シャーレに採り、こ
れに表1に示す資材を表2の使用割合で加えて混合し
た。この土壌を30℃で14日間培養し、青枯病菌数を調べ
た。その結果を表2に示す。尚、青枯病菌の検出には
の原・小野培地を用い30℃で培養2日目のコロニー数を
計測した。125 g of soil contaminated with bacterial wilt of (Example 1)
(100 g by dry weight) was taken in a large petri dish having a diameter of 158 mm, and the materials shown in Table 1 were added and mixed in the proportions shown in Table 2. This soil was cultured at 30 ° C. for 14 days, and the number of bacterial wilts was examined. The results are shown in Table 2. For the detection of bacterial wilt disease, the number of colonies on the second day of culture was counted at 30 ° C. using the Haro-Ono medium.
【0020】表2から明らかなように本発明防除材を用
いた場合、著しく青枯病菌が減少することが判る。As is clear from Table 2, the bacterial wilt disease is remarkably reduced when the control material of the present invention is used.
【0021】[0021]
【表1】 [Table 1]
【0022】[0022]
【表2】 [Table 2]
【0023】(実施例2)ハウス内(夜温20℃以上に保
持、日中は20〜35℃)で加古川沖積土壌を大型プランタ
−(長さ65cm×奥行き40cm×深さ25cm)に入れ、このプ
ランターにの青枯病菌の培養物の灌注を繰り返しすこ
とにより、青枯病菌密度が6.18×105CFU/g乾土になっ
た。この土壌は定植したトマトを夜温20℃以上に保持
して栽培すれば7〜10日で青枯病に感染する重汚染土
壌である。(Example 2) Kakogawa alluvial soil was placed in a large planter (length 65 cm x depth 40 cm x depth 25 cm) in a house (keeping the temperature at 20 ° C or higher at night, 20 to 35 ° C during the day). By repeating the irrigation of the bacterial wilt culture to this planter, the bacterial wilt density became 6.18 × 10 5 CFU / g dry soil. This soil is a heavily contaminated soil that is infected with bacterial wilt in 7 to 10 days if planted tomatoes are cultivated while being kept at a night temperature of 20 ° C or higher.
【0024】上記の青枯病発病土壌(青枯病菌数6.18×
105CFU/g乾土)を1/5000aポットに乾重で2kg 取り、化
成肥料(N、P2 O5 、K2 O、各成分10%含有)10g
及びピートモス4gを施用した。更に、これに表3に示す
各種資材10g を加え良く混合した。これをハウス内に静
置し(夜温20℃以上に保持、日中は20〜35℃)14日目に
このポットにトマトの苗(本葉4 枚の苗)4本づつを定
植し、ハウス内で35日間栽培した。試験は比較例、本発
明共全て各々5ポットづつ行なった。結果を表4に示
す。[0024] The above-mentioned bacterial wilt disease-causing soil (bacterial wilt disease number 6.18 x
10 5 CFU / g dry soil) in a 1 / 5000a pot by dry weight 2 kg, chemical fertilizer (N, P 2 O 5 , K 2 O, containing 10% of each component) 10 g
And 4 g of peat moss were applied. Furthermore, 10 g of various materials shown in Table 3 were added and mixed well. Leave this in a greenhouse (at night temperature 20 ℃ or more, 20-35 ℃ during the day) On the 14th day, plant 4 tomato seedlings (4 seedlings) in this pot, Cultivated in the house for 35 days. The test was carried out in 5 pots for each of the comparative example and the present invention. The results are shown in Table 4.
【0025】[0025]
【表3】 [Table 3]
【0026】[0026]
【表4】 [Table 4]
【0027】[0027]
【発明の効果】本発明は青枯病に対して抑制効果が高
く、繰り返して施用しても環境汚染に影響のない優れた
安価な防除材である。INDUSTRIAL APPLICABILITY The present invention is an excellent and inexpensive pesticidal material which has a high inhibitory effect against bacterial wilt disease and has no effect on environmental pollution even if it is repeatedly applied.
Claims (1)
及び/又はカニ殻とバチラス・ズブチリスとの混合物か
らなる青枯病防除材。1. A bacterial wilt control material comprising a mixture of crab shell and Bacillus cereus and / or a mixture of crab shell and Bacillus subtilis.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17810695A JP3192577B2 (en) | 1995-06-20 | 1995-06-20 | Pest control material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP17810695A JP3192577B2 (en) | 1995-06-20 | 1995-06-20 | Pest control material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH092911A true JPH092911A (en) | 1997-01-07 |
JP3192577B2 JP3192577B2 (en) | 2001-07-30 |
Family
ID=16042760
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP17810695A Expired - Fee Related JP3192577B2 (en) | 1995-06-20 | 1995-06-20 | Pest control material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3192577B2 (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000049875A1 (en) * | 1999-02-23 | 2000-08-31 | Kureha Chemical Ind Co Ltd | Plant disease control method |
JP2007261992A (en) * | 2006-03-28 | 2007-10-11 | Eisai Seikaken Kk | Soil borne disease inhibitor |
CN100404664C (en) * | 2006-06-09 | 2008-07-23 | 中国农业科学院植物保护研究所 | Biological control bacillus subtilis for crop bacterial wilt |
WO2011032330A1 (en) * | 2009-09-18 | 2011-03-24 | 南京农业大学 | Antagonistic bacteria for preventing and treating bacterial wilt disease of continuously planted tobacco and microorganism organic fertilizer thereof |
CN107142210A (en) * | 2017-04-23 | 2017-09-08 | 贵州省烟草公司黔西南州公司 | A kind of compound method of hard stalk fermentation microbial inoculum |
CN108713461A (en) * | 2018-04-24 | 2018-10-30 | 奚正华 | A kind of solanaceous vegetable bacterial wilt control method |
CN108849985A (en) * | 2018-05-30 | 2018-11-23 | 唐山市农业科学研究院 | A kind of ternary built bacteria agent and its application in bacterial wilt of ginger prevention and treatment |
-
1995
- 1995-06-20 JP JP17810695A patent/JP3192577B2/en not_active Expired - Fee Related
Cited By (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2000049875A1 (en) * | 1999-02-23 | 2000-08-31 | Kureha Chemical Ind Co Ltd | Plant disease control method |
JP2007261992A (en) * | 2006-03-28 | 2007-10-11 | Eisai Seikaken Kk | Soil borne disease inhibitor |
CN100404664C (en) * | 2006-06-09 | 2008-07-23 | 中国农业科学院植物保护研究所 | Biological control bacillus subtilis for crop bacterial wilt |
WO2011032330A1 (en) * | 2009-09-18 | 2011-03-24 | 南京农业大学 | Antagonistic bacteria for preventing and treating bacterial wilt disease of continuously planted tobacco and microorganism organic fertilizer thereof |
KR101039176B1 (en) * | 2009-09-18 | 2011-06-03 | 지앙수 뉴 그라운드 바이오퍼틸라이저 엔지니어링 센터 컴퍼니 리미티드 | Antagonistic bacteria for preventing and eliminating the bacterial wilt of continuous cropping tobacco and their microbial organic fertilizer |
EP3613843A1 (en) * | 2009-09-18 | 2020-02-26 | Nanjing Agricultural University | Antagonistic bacteria for preventing and eliminating the bacterial wilt of continuous cropping tobacco and their microbial organic fertilizer |
CN107142210A (en) * | 2017-04-23 | 2017-09-08 | 贵州省烟草公司黔西南州公司 | A kind of compound method of hard stalk fermentation microbial inoculum |
CN108713461A (en) * | 2018-04-24 | 2018-10-30 | 奚正华 | A kind of solanaceous vegetable bacterial wilt control method |
CN108849985A (en) * | 2018-05-30 | 2018-11-23 | 唐山市农业科学研究院 | A kind of ternary built bacteria agent and its application in bacterial wilt of ginger prevention and treatment |
CN108849985B (en) * | 2018-05-30 | 2021-02-26 | 唐山市农业科学研究院 | Ternary compound biological agent and application thereof in prevention and treatment of ginger bacterial wilt |
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