JPH0442355B2 - - Google Patents

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Publication number
JPH0442355B2
JPH0442355B2 JP13447183A JP13447183A JPH0442355B2 JP H0442355 B2 JPH0442355 B2 JP H0442355B2 JP 13447183 A JP13447183 A JP 13447183A JP 13447183 A JP13447183 A JP 13447183A JP H0442355 B2 JPH0442355 B2 JP H0442355B2
Authority
JP
Japan
Prior art keywords
bacteria
culture
azotobacter
knot
product
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
JP13447183A
Other languages
Japanese (ja)
Other versions
JPS6027672A (en
Inventor
Yoshimichi Monma
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.)
NIPPON RAIFU KK
Original Assignee
NIPPON RAIFU KK
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 NIPPON RAIFU KK filed Critical NIPPON RAIFU KK
Priority to JP13447183A priority Critical patent/JPS6027672A/en
Publication of JPS6027672A publication Critical patent/JPS6027672A/en
Publication of JPH0442355B2 publication Critical patent/JPH0442355B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は、微生物の混合培養物を利用し、また
必要に応じ該混合物を海緑石その他の細砕物中で
保持することにより、堆肥の腐熟促進、土壌の改
良、肥効の増進、残留農薬の無害化、病害微生物
の抑制をする資料を製造する方法を提供するもの
である。
DETAILED DESCRIPTION OF THE INVENTION The present invention utilizes a mixed culture of microorganisms and, if necessary, maintains the mixture in glauconite or other crushed materials to promote the ripening of compost, improve soil, The present invention provides a method for producing materials that enhance the effectiveness of fertilizers, render residual agricultural chemicals harmless, and suppress pathogenic microorganisms.

近年、化学肥料の多用の影響もあつて、土壌環
境の悪化、病害の多発等の弊害が重大な問題とな
つているが、本発明の資料はこれら深刻な問題を
解決するとともに、現在必要とされている堆肥の
利用を促進し、土壌を改良し、また病害微生物を
抑制する効果を有する。
In recent years, due in part to the heavy use of chemical fertilizers, adverse effects such as deterioration of the soil environment and frequent occurrence of diseases have become serious problems. It has the effect of promoting the use of compost, improving soil, and suppressing disease-causing microorganisms.

本発明の資料の製造方法は、根瘤菌とアゾトバ
クター又は光合成菌及び硫黄細菌を草木灰水溶液
に蔗糖又はマルトースを加え滅菌した培地に接種
し25℃前後で適当時間培養したものを作り、別に
硝化菌、繊維素分解菌、放線菌、糸状菌、酵母、
枯草菌、シユウドモナス菌の培養物を作り、この
培養物を上記の根瘤菌、アゾトバクター又は光合
成菌、硫黄細菌の培養物に混合して製品とし、必
要に応じ、この混合物を海緑石、大谷石、ヒル
石、貝化石、ピートモス、乾燥畜糞、石膏、麦
芽、米糖、骨粉、燻炭、草木灰から選ばれた一種
又は多数種の細砕物に蔗糖又はマンニツトを加え
たものと混合し適温の下に適当時間保持すること
を特徴とするものである。
The method for producing materials of the present invention is to inoculate root-knot bacteria, azotobacter, photosynthetic bacteria, and sulfur bacteria into a sterilized medium containing sucrose or maltose in an aqueous solution of plant ash, culture them at around 25°C for an appropriate period of time, and separately prepare nitrifying bacteria, fibrinolytic bacteria, actinomycetes, filamentous fungi, yeast,
A culture of Bacillus subtilis and Pseudomonas is made, and this culture is mixed with the above-mentioned root-knot bacteria, Azotobacter or photosynthetic bacteria, and sulfur bacteria culture to make a product. If necessary, this mixture is mixed with glauconite, Oya stone. The mixture is mixed with sucrose or mannite added to one or more crushed materials selected from vermiculite, shellfish fossils, peat moss, dried livestock dung, gypsum, malt, rice sugar, bone meal, smoky charcoal, and plant ash, and mixed at an appropriate temperature. It is characterized by being held for an appropriate period of time.

本発明で使用する微生物を例示すれば次のとお
りである。
Examples of microorganisms used in the present invention are as follows.

根瘤菌;Rhizobium Japonicum、Rhizobium
meliloti、Rhizobium trifolii、
Rhizobium leguminosarum、
Rhizobium phaseobi、Rhizobium
lupini. アゾトバクター;Azotobacter indicum、
Azotobacter vinlandi、Azotobacter
chroococcum 光合成菌;Rhodopseudomonas capsulatus、
Clostridium Butyricum、
Clostridium pasteurianum、
Clostridium aceticum. 硫黄細菌;Thiobacillus thioparus、
Thiobacillus thiooxidans、
Thiobacillus denitrificans. 硝化菌;Nitrosomonas europaea、
Nitrosomonas oligocarbogenes、
Nitrobaoter winogradskyi、
Nitrobacter agilis. 繊維素分解菌;Cellulomonas Flavigena. 放線菌;Streptomyces griseus. 糸状菌;Aspergillus Oryzae、Penicillium
patulum、Mucor mucedo、 酵母;Sacharomyces ellipsoideus. 枯草菌;Bacillus subtilis シユウドモナス菌;Pseudomonas
viscosissima、Pseudomonas
alboflava、Pseudomonas
fluorescens var、Pseudomonas
ruhlandii. その他;Bacillus polymyxa、Bacillus
circulans、Bacillus cereus、
Bacillus posteurii、Bacillus
freudenreichii、Bacillus
megaterium、 Thermoactinomyces vulgaris、(好
熱菌)Trichoderma album、
Rhizopus acidus 次に、本発明を実施した一例を述べる。
Root-knot fungi; Rhizobium Japonicum, Rhizobium
meliloti, Rhizobium trifolii,
Rhizobium leguminosarum,
Rhizobium phaseobi, Rhizobium
lupini. Azotobacter; Azotobacter indicum,
Azotobacter vinlandi, Azotobacter
chroococcum Photosynthetic bacteria; Rhodopseudomonas capsulatus,
Clostridium Butyricum,
Clostridium pasteurianum,
Clostridium aceticum. Sulfur bacteria; Thiobacillus thioparus,
Thiobacillus thiooxidans,
Thiobacillus denitrificans. Nitrifying bacteria; Nitrosomonas europaea,
Nitrosomonas oligocarbogenes,
Nitrobaoter winogradskyi,
Nitrobacter agilis. Fibrinolytic bacteria; Cellulomonas Flavigena. Actinobacteria; Streptomyces griseus. Filamentous fungi; Aspergillus Oryzae, Penicillium
patulum, Mucor mucedo, Yeast; Sacharomyces ellipsoideus. Bacillus subtilis; Pseudomonas
viscosissima, Pseudomonas
alboflava, Pseudomonas
fluorescens var, Pseudomonas
ruhlandii. Others; Bacillus polymyxa, Bacillus
circulans, Bacillus cereus,
Bacillus posteurii, Bacillus
freudenreichii, Bacillus
megaterium, Thermoactinomyces vulgaris, Trichoderma album,
Rhizopus acidus Next, an example of implementing the present invention will be described.

実施例 1 蒸留水1リツトル中で、5.6gの木灰を5分間
煮沸して過する。煮沸消毒済の容器にこの液体
を入れ、15gのマルトース又は蔗糖を加え、溶解
するまで再び5〜10間ボイルする。液温を生温か
い程度の温度まで下げた後、用意した根瘤菌
(Rhizobium)をさめた蒸留水で洗いながら接種
し、またアゾトバクター又は光合成菌及び硫黄細
菌を接種する。
Example 1 5.6 g of wood ash is boiled and filtered for 5 minutes in 1 liter of distilled water. Pour this liquid into a sterilized container, add 15g of maltose or sucrose, and boil again for 5 to 10 minutes until dissolved. After lowering the temperature of the liquid to lukewarm temperature, the prepared root-knot bacteria (Rhizobium) is inoculated while washing with cooled distilled water, and Azotobacter, photosynthetic bacteria, and sulfur bacteria are inoculated.

接種液は汚染防止の覆いを施し、温度25℃前後
で2〜5日間おく。
Cover the inoculum to prevent contamination and keep it at a temperature of around 25°C for 2 to 5 days.

根瘤菌の培養は、従来単独で培養しても充分な
増殖がなされず、良好な結果を得ることはできな
かつた。
Conventionally, when culturing root knot bacteria alone, sufficient growth was not achieved and good results could not be obtained.

しかし根瘤菌は、本法のように、アゾトバクタ
ー又は光合成菌、硫黄細菌と併用して接種するこ
とにより、充分に増殖し、強力な窒素固定作用を
有するとともに、長期保存が可能となることを発
見した。
However, it was discovered that by inoculating root-knot bacteria in combination with Azotobacter, photosynthetic bacteria, and sulfur bacteria as in this method, they can proliferate sufficiently, have a strong nitrogen-fixing effect, and can be stored for long periods of time. did.

また5.6g程度のアンモニアリン酸塩を添加す
ることによりその増殖速度は増大する。
The growth rate is also increased by adding about 5.6 g of ammonia phosphate.

2〜5日で増殖して白濁した培養液をうる。こ
の培養液は約40培に稀釈しても強力な作用を維持
する。
Proliferate in 2 to 5 days and obtain a cloudy culture solution. This culture maintains its strong effect even when diluted to about 40 ml.

また、これとは別に、Nitrobacter菌を
Cellulomonas Flavigena、Streptomyces
griseus、Aspergillus oryzae、
Thermoactinomyces vulgaris、Sacharomyces
ellipsoideus、Bacillus subtilis、Pseudomonas
viscosissimaと併用培養して培養物を得、前記培
養物と混合して製品を得た。
Apart from this, Nitrobacter bacteria
Cellulomonas Flavigena, Streptomyces
griseus, Aspergillus oryzae,
Thermoactinomyces vulgaris, Sacharomyces
ellipsoideus, Bacillus subtilis, Pseudomonas
A culture was obtained by co-cultivating with S. viscosissima, and a product was obtained by mixing with the above culture.

Nitrobacter菌も上記微生物と併用培養するこ
とにより、単独で培養した場合に比し、はるかに
良好な増殖結果が得られる。また乳酸、酪酸など
の有機酸を産生する微生物と併用して培養するこ
とは一層効果的である。
By culturing Nitrobacter bacteria in combination with the above-mentioned microorganisms, much better growth results can be obtained than when culturing them alone. Furthermore, it is even more effective to culture in combination with microorganisms that produce organic acids such as lactic acid and butyric acid.

実施例 2 実施例1で得た培養物を 細かく粉砕した海緑石、貝化石 35% 細かく分解し、中性化した水分25%のピートモ
ス 乾燥した畜糞 35% 細かく粉砕した石膏 10% 麦芽(又は米ぬか) 5% 骨 粉 5% くん炭(又は草木灰) 5% 蔗糖、マンニツト 各1% に混合し、温度25℃、湿度15%の条件下で約30日
間保持し、製品を得た。
Example 2 Glauconite and shellfish fossils obtained by finely crushing the culture obtained in Example 1 35% Finely decomposed and neutralized peat moss with a moisture content of 25% Dried animal manure 35% Finely crushed gypsum 10% Malt (or Rice bran) 5%, bone meal 5%, charcoal (or plant ash) 5%, sucrose and mannite 1% each were mixed and kept at a temperature of 25°C and humidity of 15% for about 30 days to obtain a product.

実施例2で使用する海緑石その他は細かく粉砕
されていることが必要であり、またピートモスや
畜糞は雑草の種子や有害バクテリアを殺菌するた
め、あらかじめ100℃以上の蒸気殺菌又は火力乾
燥を施こし、又は70℃以上で1週間ないしそれ以
上高温発酵をしておくことが望ましい。
The glauconite and other materials used in Example 2 must be finely pulverized, and the peat moss and livestock manure must be steam sterilized at 100°C or higher or dried by fire in order to kill weed seeds and harmful bacteria. It is desirable to strain or ferment at a high temperature of 70℃ or higher for one week or more.

実施例2の方法により、本発明の製品は長期の
活性を維持するとともに、運搬・販売に適した形
状を得ることができる。
By the method of Example 2, the product of the present invention can maintain its activity for a long period of time and can obtain a shape suitable for transportation and sale.

本発明の製品を接種して堆肥を製造すると、1
トンの堆肥に本製品10gを混入することにより堆
肥の腐熟化が促進され、従来の3分の1ないし5
分の1程度の短期間で腐熟が行われる。本製品中
のCellulomonas菌、Pseudomonas菌等の作用に
より繊維素の分解が促進され、また好熱菌、枯草
菌が増殖する。
When compost is produced by inoculating the product of the present invention, 1
By mixing 10g of this product into a ton of compost, the rottenness of the compost will be promoted, reducing the amount by one-third to five times compared to conventional methods.
Ripening takes place in a short period of time, about 1/2 the time. The action of Cellulomonas bacteria, Pseudomonas bacteria, etc. in this product promotes the decomposition of cellulose, and also causes the growth of thermophilic bacteria and Bacillus subtilis.

そのため、本発明の製品は畜糞、食品汚泥、都
市の生ゴミ、産業廃棄物等の発酵処理に抜群の効
果をもたらす。
Therefore, the product of the present invention has an outstanding effect on the fermentation treatment of livestock manure, food sludge, city garbage, industrial waste, etc.

本発明の製品は、堆肥材料や肥料に接種して使
用するほか、土壌に散布または潅注して使用し、
化学肥料及び農薬の多用により著しく減少した土
壌中の根瘤菌、光合成細菌その他の有効微生物を
補強し、腐植の増加と土壌の団粒構造を作り、土
壌の保水性と通気性、透水性を改良し、対旱魃、
対冷性を強化し、肥効の増進をもたらす。
The product of the present invention can be used by inoculating compost materials and fertilizers, as well as by spraying or irrigating the soil.
Reinforce root-knot bacteria, photosynthetic bacteria, and other effective microorganisms in the soil, which have decreased significantly due to heavy use of chemical fertilizers and pesticides, increase humus and create a soil aggregate structure, improving soil water retention, air permeability, and water permeability. against drought,
Strengthens cold resistance and improves fertilizing effect.

また、本発明の製品は、Pseudomonas
ruhlandii等が残留農薬等の有害物質の分解を促
進し、これを無毒化するとともに、酸性・硬化し
た土壌を蘇らせることができる。
In addition, the product of the present invention can be used to treat Pseudomonas
ruhlandii, etc., promote the decomposition of harmful substances such as residual pesticides, making them non-toxic, and can revitalize acidic and hardened soil.

さらに、本発明の製品は、植物の種子に散布
し、又は植物の枝、茎、葉に散布して使用するこ
とができる。
Furthermore, the product of the present invention can be used by spraying on the seeds of plants, or on the branches, stems, and leaves of plants.

本発明の製品の使用により、植物の有害微生物
の繁殖を抑制し、白絹病、菌核病、根こぶ病、紋
羽病、ふらん病、モザイク病の抑制に効果があ
る。
Use of the product of the present invention is effective in suppressing the proliferation of harmful microorganisms in plants, and in suppressing white silk disease, sclerotium disease, clubroot disease, crest disease, flannel disease, and mosaic disease.

特にモザイク病は全国的に出現し、トマトの重
要な病害であるとともに、タバコ、キユウリ、ジ
ヤガイモ、メロン、ピーマン、ナス等にも発生す
る。しかし、ウイルスによる病害であるために、
その防除は非常に困難であり、適切な対応策は皆
無とされていた。本発明の製品はその解決を初め
て、可能とした。
In particular, mosaic disease appears nationwide and is an important disease of tomatoes, but also occurs on tobacco, cucumbers, potatoes, melons, green peppers, eggplants, etc. However, since it is a disease caused by a virus,
It is extremely difficult to control it, and there were no appropriate countermeasures. The product of the present invention has made this solution possible for the first time.

トマト、モザイク病の伝染形態は移植、摘芽等
の栽培管理時に於ける接触伝染、病株から採種し
た種子による種子伝染、土壌中の病株の残留株等
による土壌伝染があるが、このうち土壌伝染が最
も多く、一種の土壌病害といえるものである。
The modes of transmission of tomato mosaic disease include contact transmission during cultivation management such as transplanting and budding, seed transmission through seeds collected from diseased plants, and soil transmission through residual strains of diseased plants in the soil. It is most commonly transmitted and can be considered a type of soil disease.

ところが、東京都農業試験場におけるトマトの
肥効試験の結果では、対照区(化成品)では74株
中6株のモザイク病罹病株が出現したが、同時に
行つた本発明製品区では74株中1株しか罹病が見
い出されなかつた。同試験では種子伝染、接触伝
染が考えられず、モザイク病ウイルスが
olpidium菌、線虫等他の微生物の体内に寄生す
ることから、本製品中のBacillua菌
Trichoderma菌、Streptomyces菌、Rhizopus菌
その他の微生物により、ウイルス寄生菌の活動が
抑制された結果、罹病しなかつたものと考えられ
る。
However, according to the results of a tomato fertilizer efficacy test at the Tokyo Metropolitan Agricultural Experiment Station, 6 out of 74 plants infected with mosaic disease appeared in the control plot (chemical products), but 1 out of 74 in the inventive product plot, which was conducted at the same time. Only the plants were found to be affected. In this test, seed transmission and contact transmission were not considered, and mosaic disease virus was detected.
Bacillus bacteria in this product are parasitic to other microorganisms such as olpidium bacteria and nematodes.
It is thought that the virus parasitic fungi were suppressed by Trichoderma, Streptomyces, Rhizopus, and other microorganisms, resulting in no illness.

Claims (1)

【特許請求の範囲】[Claims] 1 根瘤菌とアゾトバクター又は光合成菌及び硫
黄細菌を草木灰水溶液に蔗糖又はマルトースを加
え滅菌した培地に接種し25℃前後で適当時間培養
したものを作り、別に硝化菌、繊維素分解菌、放
線菌、糸状菌、酵母、好熱菌、枯草菌、シユウド
モナス菌の培養物を作り、この培養物を上記の根
瘤菌、アゾトバクター又は光合成菌、硫黄細菌の
培養物に混合して製品とし、必要に応じ、この混
合物を海緑石、大谷石、ヒル石、貝化石、ピート
モス、乾燥畜糞、石膏、麦芽、米糖、骨粉、燻
炭、草木灰から選ばれた一種又は多数種の細砕物
に蔗糖又はマンニツトを加えたものと混合し適温
の下に適当時間保持することを特徴とする。堆肥
の腐熟促進、土壌の改良、肥効の増進、残留農薬
の無害化、病害微生物を抑制する資料を製造する
方法。
1. Inoculate root-knot bacteria and Azotobacter or photosynthetic bacteria and sulfur bacteria into a sterilized medium by adding sucrose or maltose to an aqueous plant ash solution and culture at around 25°C for an appropriate period of time. Create a culture of filamentous fungi, yeast, thermophilic bacteria, Bacillus subtilis, and Pseudomonas bacteria, and mix this culture with the above-mentioned root-knot bacteria, Azotobacter or photosynthetic bacteria, and sulfur bacteria cultures to make a product, and as necessary, This mixture is mixed with sucrose or mannitrate into one or more crushed materials selected from glauconite, Oya stone, vermiculite, fossil shells, peat moss, dried livestock dung, gypsum, malt, rice sugar, bone meal, smoky charcoal, and plant ash. It is characterized by mixing it with the added ingredients and keeping it at an appropriate temperature for an appropriate period of time. A method for producing materials that accelerate the ripening of compost, improve soil, increase the effectiveness of fertilizers, detoxify residual agricultural chemicals, and suppress disease-causing microorganisms.
JP13447183A 1983-07-25 1983-07-25 Manufacture of material for accelerating compost rottenness,improving soil, increasing fertilizer effect, decontaminating residual agricultural drug and controlling disease microbes by use of microbial culture Granted JPS6027672A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13447183A JPS6027672A (en) 1983-07-25 1983-07-25 Manufacture of material for accelerating compost rottenness,improving soil, increasing fertilizer effect, decontaminating residual agricultural drug and controlling disease microbes by use of microbial culture

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13447183A JPS6027672A (en) 1983-07-25 1983-07-25 Manufacture of material for accelerating compost rottenness,improving soil, increasing fertilizer effect, decontaminating residual agricultural drug and controlling disease microbes by use of microbial culture

Publications (2)

Publication Number Publication Date
JPS6027672A JPS6027672A (en) 1985-02-12
JPH0442355B2 true JPH0442355B2 (en) 1992-07-13

Family

ID=15129092

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13447183A Granted JPS6027672A (en) 1983-07-25 1983-07-25 Manufacture of material for accelerating compost rottenness,improving soil, increasing fertilizer effect, decontaminating residual agricultural drug and controlling disease microbes by use of microbial culture

Country Status (1)

Country Link
JP (1) JPS6027672A (en)

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CA1335366C (en) * 1986-08-19 1995-04-25 Joseph Kloepper Plant growth promoting rhizobacteria for agronomic nonroot crops
JPS63218593A (en) * 1987-03-06 1988-09-12 エヌ・アイ・テクノ・セ−ルス株式会社 Accelerator for composting garbage
JPH0226886A (en) * 1988-07-13 1990-01-29 Shigekiyo Tsuge Fertilizer
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WO1995004814A1 (en) * 1993-08-06 1995-02-16 International Tlb Research Institute, Inc. Recombinant microbial fertilizer and methods for its production
US7037494B2 (en) * 1997-10-14 2006-05-02 The Board Of Regents Of The University Of Texas System Formulations and methods for insect control
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