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JPS6023832B2 - Protozoa and micrometazoa culture equipment - Google Patents
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JPS6023832B2 - Protozoa and micrometazoa culture equipment - Google Patents

Protozoa and micrometazoa culture equipment

Info

Publication number
JPS6023832B2
JPS6023832B2 JP15019180A JP15019180A JPS6023832B2 JP S6023832 B2 JPS6023832 B2 JP S6023832B2 JP 15019180 A JP15019180 A JP 15019180A JP 15019180 A JP15019180 A JP 15019180A JP S6023832 B2 JPS6023832 B2 JP S6023832B2
Authority
JP
Japan
Prior art keywords
tank
protozoa
culture
micrometazoa
bait
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
JP15019180A
Other languages
Japanese (ja)
Other versions
JPS5774082A (en
Inventor
立夫 角野
一郎 中島
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.)
Hitachi Ltd
Original Assignee
Hitachi Plant Engineering and Construction 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 Hitachi Plant Engineering and Construction Co Ltd filed Critical Hitachi Plant Engineering and Construction Co Ltd
Priority to JP15019180A priority Critical patent/JPS6023832B2/en
Publication of JPS5774082A publication Critical patent/JPS5774082A/en
Publication of JPS6023832B2 publication Critical patent/JPS6023832B2/en
Expired legal-status Critical Current

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  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Micro-Organisms Or Cultivation Processes Thereof (AREA)

Description

【発明の詳細な説明】 本発明は、餌を摂食しやすい状態で与えることにより原
生動物や微小後生動物を効果的に繁殖させることのでき
る培養装置に関する。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a culture device that can effectively breed protozoa and micrometazoans by providing food in an easily ingestible state.

原生動物及び微小後生動物は細菌、酵母、放線菌、藻類
、カビ等を餌として糠食している。
Protozoa and micrometazoa eat rice bran, using bacteria, yeast, actinomycetes, algae, mold, etc. as food.

従って、これらの動物を培養するには、動物培養槽内で
同時に餌を培養する方式と、餌培養槽を別個に設ける方
式とがある。しかしながらいずれの方式でも、餌が凝集
しやすく、そのフロツクサィズが原生動物の細胞口、微
小後生動物の口より大きくなると、摂食し難くなり、こ
れらの動物の比増殖速度が低下し、これらの動物の濃度
が低下する。本発明の目的は、前記従来技術の欠点を解
消し、原生動物及び微小後生動物を安定して高い濃度で
培養する装置を提供することにある。なお、本明細書に
おいて、微小後生動とは例えば袋形動物、環形動物、節
足動物等、大きさ数肋以下の微4・後生動物をいう。
Therefore, in order to culture these animals, there are two methods: one is to simultaneously culture food in an animal culture tank, and the other is to provide a separate food culture tank. However, in either method, if the food tends to aggregate and the floc size becomes larger than the cell mouth of protozoa or the mouth of micrometazoa, it becomes difficult to feed, and the specific growth rate of these animals decreases. concentration decreases. SUMMARY OF THE INVENTION An object of the present invention is to eliminate the drawbacks of the prior art and provide an apparatus for stably culturing protozoa and micrometazoans at high concentrations. In this specification, micrometazoans refer to micrometazoans having a size of a few ribs or less, such as sacs, annelids, and arthropods.

上記目的は、本発明によれば、餌の培養又は調整槽と動
物の培養槽との間に餌のフロックサィズを動物の口より
4・さくする手段、即ち微細化槽を設けることによって
達成される。
According to the present invention, the above object is achieved by providing a means for reducing the floc size of the feed by 4 mm from the animal's mouth, that is, a micronization tank between the feed culture or adjustment tank and the animal culture tank. Ru.

本発明に使用する微細イ材曹‘ま、機械凝梓装置又は超
音波発生装瞳等、餌を含む培養液に敷断力を与えうる装
置を有する糟であればよい。
The fine material used in the present invention may be any sieve having a device capable of applying a breaking force to the culture solution containing food, such as a mechanical flocculation device or an ultrasonic generator.

フロックの微細化を容易にするため、糟に邪魔板を設け
ておくのも有利である。次に図面に基づいて本発明を詳
述する。
It is also advantageous to provide a baffle plate in the mill to facilitate finer flocs. Next, the present invention will be explained in detail based on the drawings.

第1図は本発明の装置の系統図である。FIG. 1 is a system diagram of the apparatus of the present invention.

第1図において餌の培養又は調整槽1は、細菌、酵母、
放線菌、藻類、カビ類等の餌を培養する糟、又は廃水の
生物処理による余剰汚泥、廃水の初次汚泥等をためてお
く調整槽である。培養又は調整された餌は、微細化槽2
に送られ、ここで超音波処理、機械擬洋等により微細化
され、動物が摂食しやすい大きさにする。原生動物の細
胞口や微4・後生動物の口の大きさは、これらの動物の
種類によって著しく異なり、大きいもので500〃、4
・さし、もので50#以下のものまである。従って、動
物培養槽3で培養する原生動物、微小後生動物の種類に
よって餌の大きさの上限が異なり、餌の微細化の条件が
異なる。これらの条件及び餌のフロツクサィズを考慮し
て、縄杵の強度を適切に選択する。第2図及び第3図は
、タービン形蝿杵槽4から成る微細化槽を示すものであ
る。
In FIG. 1, a bait culture or adjustment tank 1 includes bacteria, yeast,
This is an adjustment tank that stores sludge for cultivating food such as actinomycetes, algae, and molds, surplus sludge from biological treatment of wastewater, and primary sludge of wastewater. The cultured or adjusted bait is placed in the micronization tank 2.
There, they are pulverized by ultrasonic treatment, mechanical simulation, etc., and made into a size that is easy for animals to eat. The size of the cytostomes of protozoa and the mouths of microzoans and metazoans vary significantly depending on the type of these animals, with the largest being 500 mm and 4 mm.
・There are cuttings of 50# or less. Therefore, the upper limit of the size of the bait differs depending on the type of protozoa or micrometazoan cultured in the animal culture tank 3, and the conditions for refining the bait differ. The strength of the rope pestle should be selected appropriately, taking into consideration these conditions and the floc size of the bait. 2 and 3 show a refining tank consisting of a turbine type fly punch tank 4. FIG.

この凝幹槽の壁には邪魔板6が設けられ、糟の中央に平
羽根5が設けられている。槽内の餌は平羽根5の回転に
より礎梓され、更に邪魔板6への衝突により微細化され
る。図面にはタービン形燈梓機を設けた場合を例示した
が、蝿梓機は、擢形澄洋機、プロペラ型蝿拝機、膿気に
よる鰯梓機等でもよく、餌に奥断力を与えて微細化する
装置であればよい。
A baffle plate 6 is provided on the wall of this stem tank, and a flat blade 5 is provided in the center of the mulch. The bait in the tank is crushed by the rotation of the flat blades 5, and further refined by colliding with the baffle plate 6. The drawing shows an example in which a turbine-type tomo-azusa machine is provided, but the fly-azusa machine may also be a sardine-type sardine machine, a sardine-type sardine machine, a propeller-type sardine machine, etc., which give deep cutting force to the bait. Any device that can be used for miniaturization is sufficient.

このような微細化槽を通過させることにより、餌が常に
動物に摂食されやすい大きさで提供されるので、動物の
比増殖速度を低下することなく、動物を安定して高い濃
度で培養することができる。
By passing the food through such a miniaturized tank, the food is always provided in a size that is easily ingested by the animals, so animals can be cultured at a stable high concentration without reducing the specific growth rate of the animals. be able to.

次に、実施例に基づいて本発明を詳述するが、本発明は
これに限定されるものではない。
Next, the present invention will be described in detail based on Examples, but the present invention is not limited thereto.

実施例 1 べプトン、肉エキスを主体とした培地で黄色菌(Fia
vo戊cterium)を培養し、微細化槽で超音波処
理し、餌を5一以下にし、この餌でゾウリ虫(Para
meci山m)を培養した。
Example 1 A medium containing beptone and meat extract as the main ingredient
vocterium), ultrasonication is carried out in a micronization tank, the food is reduced to less than 5, and this food is used to
meciyama m) was cultured.

それぞれの糟の運転条件は下記のとおりである:餌の培
養槽:滞留時間、6時間、温度:2000溶存酸素 8
.8の902/そ餌の微細化槽:滞留時間、10分 超音波処理:磁歪型microhorn 20KHz、50W ゾウリ虫の培養槽:滞留時間、1独特間、温度20oo
、溶存酸素8.&902′そ超音波処理において、過酸
化水素の発生を硫酸チタンによる比色定量法を用いて調
べたが、処理時間10分で2.5脚と生物には影響のな
い濃度であつた。
The operating conditions for each pot are as follows: Bait culture tank: Residence time: 6 hours; Temperature: 2000℃ dissolved oxygen 8
.. 902 of 8/Sea bait micronization tank: Residence time, 10 minutes Ultrasonic treatment: Magnetostrictive microhorn 20KHz, 50W Elephant insect culture tank: Residence time, 1 unique time, temperature 20oo
, dissolved oxygen8. &902' During the ultrasonic treatment, the generation of hydrogen peroxide was investigated using a colorimetric method using titanium sulfate, and the concentration was 2.5 per oxide in 10 minutes, which had no effect on living organisms.

比較のため、微細イり曹を省いた以外は、前記と同じ条
件で(従来の2糟式)培養を行なった。
For comparison, culture was carried out under the same conditions as above (conventional two-pot method) except that the fine charcoal was omitted.

本発明方法の場合には、餌を5ム以下で供給でき、ゾウ
リ虫を1×1ぴ匹/の‘の濃度で連続培養できた。これ
に対して、従来法では餌がフロキュレーションし、最大
500仏程度にまでなり、ゾウリ虫の濃度は1×1の匹
/舷まで低下した。実施例 2べプトン、肉エキスを主
体とした培地で小球菌(Micr似occ雌Varia
nsATCC399)を培養槽中で連続培養し、微細イ
○漕中で機械燈拝し、餌を60山以下にし、動物培養槽
中でッリガネ虫(Vemcella)を培養した。
In the case of the method of the present invention, feed could be supplied in a quantity of 5 μm or less, and the parasitic insects could be continuously cultured at a concentration of 1 × 1 insect/cm. On the other hand, with the conventional method, the bait flocculated to a maximum of about 500 larvae, and the concentration of weevil insects decreased to 1 × 1 insect/ship. Example 2 Micrococcus (Micr-like occ female Varia
nsATCC399) was continuously cultured in a culture tank, mechanically illuminated in a micro-cell, feed was reduced to 60 mounds or less, and Vemcella was cultured in an animal culture tank.

鷹枠は第2図及び第3図に示すタービン形燈梓機を用い
て行なった。それぞれの檀の運転条件は下記のとおりで
ある。餌の倍養:滞留時間、3時間温度 2000 溶存酸素 8.8Moo2′〆 餌の微細イ○菅:滞留時間、1時間 120仇pm ツリガネ虫の培養槽:滞留時間、1幼時間温度 20つ
○ 溶存酸素 8.&902/ク 微細化槽を省いた以外は、前記と同じ条件で(従来の2
槽式)培養を行なった。
The hawk frame was made using a turbine-type tomazusa machine shown in Figures 2 and 3. The operating conditions for each dan are as follows. Feeding doubling: Residence time, 3 hours Temperature 2000 Dissolved oxygen 8.8Moo2'〆Feed fine ○ tube: Residence time, 1 hour 120 pm Culture tank for turret bugs: Residence time, 1 hour temperature 20○ Dissolved oxygen 8. &902/k Under the same conditions as above except that the atomization tank was omitted (conventional 2
(tank type) culture was performed.

本発明によれば、餌を60山以下で供総合でき、ッIJ
ガネ虫を1×1ぴ匹/泌の濃度で連続培養できた。
According to the present invention, bait can be prepared in less than 60 piles, and
It was possible to continuously culture worms at a concentration of 1 x 1 insect/secretion.

これに対して従来法では餌が凝集し、最大で300ム程
度にまでなり、ッリガネ虫の濃度は1×10匹/私まで
低下した。このように、本発明によれば原生動物や微小
後生動物を安定して高い濃度で培養することができる。
On the other hand, in the conventional method, the bait aggregated to a maximum of about 300 ml, and the concentration of worms decreased to 1 x 10 insects/me. As described above, according to the present invention, protozoa and micrometazoans can be stably cultured at high concentrations.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の培養装置の系統図、第2図はタービン
形蝿梓槽の平面図、第3図は第2図のタービン形燈梓槽
の略示断面図である。 符号の説明、1・・・・・・餌の培養又は調整槽、2・
・・・・・微細化槽、3・・・・・・動物培養槽、4…
・・・タービン形蝿梓槽、5・・・・・・平羽根、6・
・・・・・邪魔板。 第1図第2図 第3図
FIG. 1 is a system diagram of the culture apparatus of the present invention, FIG. 2 is a plan view of a turbine-type fly bean tank, and FIG. 3 is a schematic sectional view of the turbine-type fly bean tank shown in FIG. 2. Explanation of symbols, 1...Food culture or adjustment tank, 2.
...Minimization tank, 3...Animal culture tank, 4...
...Turbine type fly azusa tank, 5...Flat blade, 6.
...Baffle board. Figure 1 Figure 2 Figure 3

Claims (1)

【特許請求の範囲】 1 原生動物や微小後生動物が摂食する細菌、酵母、放
線菌、藻類、カビ類等の餌を培養又は調整する槽と、そ
の餌を供給することにより原生動物や微小後動物を繁殖
させる槽との間に、餌微細化槽を設けたことを特徴とす
る原生動物及び微小後生動物の培養装置。 2 餌微細化槽が超音波発生装置又は機械撹拌装置を有
する槽である特許請求の範囲第1項記載の培養装置。
[Scope of Claims] 1. A tank for culturing or preparing food such as bacteria, yeast, actinomycetes, algae, molds, etc. that protozoa and micrometazoa feed on, and a tank for culturing or preparing food such as bacteria, yeast, actinomycetes, algae, and molds that protozoa and micrometazoa feed on, and A culture device for protozoa and micrometazoans, characterized in that a bait atomization tank is provided between a tank for breeding metazoa. 2. The culture device according to claim 1, wherein the bait atomization tank is a tank equipped with an ultrasonic generator or a mechanical stirring device.
JP15019180A 1980-10-28 1980-10-28 Protozoa and micrometazoa culture equipment Expired JPS6023832B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15019180A JPS6023832B2 (en) 1980-10-28 1980-10-28 Protozoa and micrometazoa culture equipment

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15019180A JPS6023832B2 (en) 1980-10-28 1980-10-28 Protozoa and micrometazoa culture equipment

Publications (2)

Publication Number Publication Date
JPS5774082A JPS5774082A (en) 1982-05-10
JPS6023832B2 true JPS6023832B2 (en) 1985-06-10

Family

ID=15491499

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15019180A Expired JPS6023832B2 (en) 1980-10-28 1980-10-28 Protozoa and micrometazoa culture equipment

Country Status (1)

Country Link
JP (1) JPS6023832B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005073134A1 (en) 2004-02-02 2005-08-11 Kurita Water Industries Ltd. Process for biological treatment of organic waste water and apparatus therefor

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19524307A1 (en) 1995-07-07 1997-01-09 Hoechst Ag Process for the mass cultivation of ciliates
CN101175700B (en) 2005-04-12 2011-04-27 栗田工业株式会社 Method for biological disposal of organic wastewater and biological disposal apparatus
CN101374772B (en) * 2006-02-03 2011-09-07 栗田工业株式会社 Method of biologically treating organic waste water
KR100903691B1 (en) 2008-09-12 2009-06-18 한국농어촌공사 Cultivation apparatus of red tide and green algae causes and protozoa predators capable of predating them

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2005073134A1 (en) 2004-02-02 2005-08-11 Kurita Water Industries Ltd. Process for biological treatment of organic waste water and apparatus therefor
EP2447222A2 (en) 2004-02-02 2012-05-02 Kurita Water Industries Ltd. Process for biological treatment of organic waste water and apparatus therefor
EP2447223A2 (en) 2004-02-02 2012-05-02 Kurita Water Industries Ltd. Process for biological treatment of organic waste water and apparatus therefor

Also Published As

Publication number Publication date
JPS5774082A (en) 1982-05-10

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