CN106719442A - A kind of method that man-made drugs' control produces Artemia cysts - Google Patents

A kind of method that man-made drugs' control produces Artemia cysts Download PDF

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Publication number
CN106719442A
CN106719442A CN201611069293.4A CN201611069293A CN106719442A CN 106719442 A CN106719442 A CN 106719442A CN 201611069293 A CN201611069293 A CN 201611069293A CN 106719442 A CN106719442 A CN 106719442A
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China
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artemia
seawater
during
cysts
man
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Application number
CN201611069293.4A
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Chinese (zh)
Inventor
柴英辉
周文礼
高金伟
窦勇
贾旭颖
孙金辉
李霞
孙朦朦
于宏
宋虹
刘胜男
韦永春
渠佳豪
周莹莹
张文慧
薄香兰
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Tianjin Agricultural University
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Tianjin Agricultural University
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Priority to CN201611069293.4A priority Critical patent/CN106719442A/en
Publication of CN106719442A publication Critical patent/CN106719442A/en
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01KANIMAL HUSBANDRY; CARE OF BIRDS, FISHES, INSECTS; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
    • A01K67/00Rearing or breeding animals, not otherwise provided for; New breeds of animals
    • A01K67/033Rearing or breeding invertebrates; New breeds of invertebrates

Abstract

Have the present invention relates to the method that a kind of man-made drugs control produces Artemia cysts, including step:(1) configuration of Artemia cysts seawater;(2) hatching of artemia nauplii;(3) nursing of artemia nauplii and pseudimago early stage;(4) artemia imago is fed and is hatched, it is 20 ‰ 60 ‰ that seawater keeps salinity in whole breeding process, pH is 7.5 8.5, dissolved oxygen concentration is 4mg/L 6mg/L, water temperature is 24.5 26.5 DEG C, feed is grouper fermented feed during artemia imago is fed, while adding Fe EDTA in the seawater or adding trehalose, or adds Fe EDTA and trehalose simultaneously.The present invention is while salinity, pH, intensity of illumination, temperature, dissolved oxygen, feed nutrition factor is controlled, then Fe EDTA or trehalose are added in breeding seawater, solves the problems, such as that artemia resting egg yield under the conditions of propagating artificially is relatively low.

Description

A kind of method that man-made drugs' control produces Artemia cysts
Technical field
Artemia reproductive technology field of the present invention, a kind of method that especially man-made drugs' control produces Artemia cysts.
Background technology
Artemia nauplii is typically used as the life food of aquaculture, especially as ocean fish, morning in brine shrimp stage The life food of phase, cut-off is current, aquaculture application mostly to freeze based on big artemia, Artemia cysts lie substantially in from The situation so bred, manually fish for, the ovum that artemia is produced under natural conditions is divided into summer egg and resting egg, resting egg under natural conditions The quantity of generation is very low, and resting egg exactly market sale, and the ovum of long-distance transport, market demand is very big, current user's purchase It can only be single use to enter after Artemia cysts, it is impossible to enough to realize by hatching to nauplius, to pseudimago, to adult, then To recycling for Artemia cysts, it is impossible to realize that Artemia cysts are manually produced, to the nursing of ocean fish, brine shrimp bring compared with Production cost high, to solve the problems, such as that artemia produces resting egg wretched insufficiency, develops a kind of man-made drugs' control and produces artemia The method of resting egg is always the direction that those skilled in the art make great efforts.
The content of the invention
It is an object of the invention to overcome the deficiencies in the prior art, there is provided a kind of man-made drugs' control produces Artemia cysts Method.
The present invention solves its technical problem and takes following technical scheme to realize:
A kind of method that man-made drugs' control produces Artemia cysts, including step is as follows:
(1) configuration of Artemia cysts seawater:Running water adds sodium hypochlorite to be aerated 24 hours, and sea crystal configuration is added afterwards It is 20 ‰ -60 ‰ artificial sea water into salinity, then proceedes to aeration 24 hours, the pH of control seawater is extra large between 7.5-8.5 Between 4mg/L---6mg/L, water temperature is between 24.5-26.5 DEG C for the concentration of water dissolves oxygen;
(2) hatching of artemia nauplii:The Artemia cysts that will be bought are put into the seawater for having configured, and are delivered density and are The seawater that 1L is configured adds 1g artemia cysts, while adding 1g sodium acid carbonates, brooding time to keep illumination during being 24h, hatching Intensity is put on to 28 DEG C water temperature between 1000-2000Lux, keeps constantly inflation preventing and treating artemia cysts to sink during hatching Bottom, resting egg hatches into artemia nauplii completely after 24h;
(3) nursing of artemia nauplii and pseudimago early stage,
1. the human configuration sea conditions for cultivating be pH between 7.5-8.5, dissolved oxygen concentration is maintained at 4mg/L-6mg/L Between, water temperature is maintained between 24.5 DEG C -26.5 DEG C;Intensity of illumination is maintained between 800-2000Lux;
2. cultivation density is 7-10/ml;
3. breeding bait and injected volume:
A. after artemia hatching within 24 hours without feeding, during the nauplius of-the five day second day, with Isochrysis galbana Raise, each consumption is:During breeding water body 1L, the Isochrysis galbana 1ml after centrifugation, three times a day timing bait throwing in;
B. after nauplius during the pseudimago of-the ten day the 6th day, raised with epinephelus feed, each consumption is:Support When growing water body 8L, the epinephelus feed that market is bought is pulverized last 0.5g, is fed at twice daily;
(4) artemia imago is fed and is hatched,
1. the seawater that will be configured during above-mentioned artemia nauplii and pseudimago keeps intensity of illumination in 800-2000Lux Between;
2. breeding bait and injected volume:Raised with grouper fermented feed, each consumption of grouper fermented feed is:Cultivation During water body 8L, each feeding volume is 12ml, twice a day timing bait throwing in;
3. in whole adult breeding process, Fe-EDTA is added in the seawater of above-mentioned cultivation, concentration reaches in making seawater 15mg-45mg/L, or trehalose is added, concentration reaches 5mg-15mg/L in making seawater, or adds Fe-EDTA simultaneously, makes seawater Middle concentration reaches 15mg-45mg/L and adds trehalose, and concentration reaches 5mg-15mg/L in making seawater, and cultivation is opened after 12 days or so Begin to lay eggs, the yield of Artemia cysts reaches more than 60%.
And, the B step nursing processes 3. walked in the step (3), and during the artemia imago of (4) step is fed often It is secondary feed before, to carry out clear up residual bait and excrement.
And, the grouper fermented feed 2. walked in the step (3) is specifically included by mass fraction composition such as the following group Part:0.5 part of 1 part of brown sugar, 20 parts of epinephelus feed, 500 parts of distilled water, 15 parts of sodium chloride and bacillus powder, said mixture Aeration is after 4 hours, then through 30 DEG C of sealing and fermentings 24 hours, wherein epinephelus feed was bought by market.
And, the optimum salinity of the artificial seawater of all steps is 30 ‰.
And, optimal Fe-EDTA additions are that concentration reaches 30mg/L in making seawater in the 3. step of the step (4); Optimal trehalose addition is that concentration reaches 10mg/L in making seawater..
Advantages and positive effects of the present invention are:
The present invention is realized by controlling the same of the factors such as salinity, pH, intensity of illumination, temperature, dissolved oxygen, feed nutrition When, then Fe-EDTA, trehalose are added, solve the problems, such as that artemia resting egg yield under the conditions of propagating artificially is relatively low.
Specific embodiment
The embodiment of the present invention is further described below, it is emphasized that, implementation below is illustrative, and It is not limited, it is impossible in this embodiment as limitation of the invention.
A kind of method that man-made drugs' control produces Artemia cysts, including step is as follows:
(1) configuration of Artemia cysts seawater:Running water adds sodium hypochlorite to be aerated 24 hours, and sea crystal configuration is added afterwards It is 20 ‰ -60 ‰ artificial sea water into salinity, then proceedes to aeration 24 hours, the pH of control seawater is extra large between 7.5-8.5 Between 4mg/L-6mg/L, water temperature is between 24.5-26.5 DEG C for the concentration of water dissolves oxygen;
(2) hatching of artemia nauplii:The Artemia cysts that will be bought are put into the seawater for having configured, and are delivered density and are The seawater that 1L is configured adds 1g artemia cysts, while adding 1g sodium acid carbonates, brooding time to keep illumination during being 24h, hatching Intensity is put on to 28 DEG C water temperature between 1000-2000Lux, keeps constantly inflation preventing and treating artemia cysts to sink during hatching Bottom, resting egg hatches into artemia nauplii completely after 24h;
(3) nursing of artemia nauplii and pseudimago early stage,
1. the human configuration sea conditions for cultivating be pH between 7.5-8.5, dissolved oxygen concentration is maintained at 4mg/L-6mg/L Between, water temperature is maintained between 24.5 DEG C -26.5 DEG C;Intensity of illumination is maintained between 800-2000Lux;
2. cultivation density is 7-10/ml;
3. breeding bait and injected volume:
A. after artemia hatching within 24 hours without feeding, during the nauplius of-the five day second day, with Isochrysis galbana Raise, each consumption is:During breeding water body 1L, the Isochrysis galbana 1ml after centrifugation, three times a day timing bait throwing in;
B. after nauplius during the pseudimago of-the ten day the 6th day, raised with epinephelus feed, each consumption is:Support When growing water body 8L, the epinephelus feed that market is bought is pulverized last 0.5g, is fed at twice daily, and feed every time Before, clear up residual bait and excrement;
(4) artemia imago is fed and is hatched,
1. by the above-mentioned seawater holding intensity of illumination being configured between 800-2000Lux;
2. breeding bait and injected volume:Raised with grouper fermented feed, wherein, grouper fermented feed is specifically included: 1g brown sugar, 20g epinephelus feeds, distilled water 500ml, sodium chloride 15g and bacillus powder 0.5g, said mixture aeration 4 are small When, 30 DEG C of sealing and fermentings 24 hours, each consumption of grouper fermented feed is:During breeding water body 8L, each feeding volume is 12ml, Twice a day timing bait throwing in;
3. in whole breeding process, Fe-EDTA is added in the seawater of above-mentioned cultivation, concentration reaches in making seawater 15mg-45mg/L, or trehalose is added, concentration reaches 5mg-15mg/L in making seawater, or adds Fe-EDTA simultaneously, makes seawater Middle concentration reaches 15mg-45mg/L and adds trehalose, and concentration reaches 5mg-15mg/L in making seawater, and cultivation is opened after 12 days or so Begin to lay eggs, wherein, the yield of Artemia cysts reaches more than 60%.
In specific implementation of the invention, the optimum salinity of the artificial seawater of sea crystal configuration is in the step (1) 30‰。
In specific implementation of the invention, optimal Fe-EDTA additions are in making seawater in 3. the walking of the step (4) Concentration reaches 30mg/L;Optimal trehalose addition is that concentration reaches 10mg/L in making seawater;
Embodiment one
The salinity of seawater is 7.5-8.5 for 30, pH;The concentration 4mg/L-6mg/L of dissolved oxygen;Water temperature is 24.5-26.5 DEG C; Intensity of illumination is 800-2000Lux;Artemia culture initial density is 8/ml.Raised with Isochrysis galbana before artemia pseudimago Support, consumption is:During breeding water body 8L, 8ml after centrifugation, three times a day timing bait throwing in;Raised with grouper in the artemia pseudimago phase Material is raised, and consumption is:During breeding water body 8L, pulverize last 1g, twice a day timing bait throwing in.In the adult stage, with grouper Fermented feed is raised, and each consumption is:During breeding water body 8L, 12ml, twice a day timing bait throwing in;
In adult stage water body also added with Fe-EDTA concentration be 30mg/L,
Any medicine group no added compared to the same period, egg laying rate of red swamp increased 53.8%
Embodiment two
The salinity of seawater is 7.5-8.5 for 30, pH;The concentration 4mg/L-6mg/L of dissolved oxygen;Water temperature is 24.5-26.5 DEG C; Intensity of illumination is 800-2000Lux;Artemia culture initial density is 8/ml.Raised with Isochrysis galbana before artemia pseudimago Support, consumption is:During breeding water body 8L, 8ml after centrifugation, three times a day timing bait throwing in;Raised with grouper in the artemia pseudimago phase Material is raised, and consumption is:During breeding water body 8L, pulverize last 1g, twice a day timing bait throwing in.In the adult stage, with grouper Fermented feed is raised, and each consumption is:During breeding water body 8L, 12ml, twice a day timing bait throwing in;
In adult stage water body also added with trehalose concentration be 10mg/L,
Any medicine group no added compared to the same period, egg laying rate of red swamp increased 49.3%
Embodiment three
The salinity of seawater is 7.5-8.5 for 30, pH;The concentration 4mg/L-6mg/L of dissolved oxygen;Water temperature is 24.5-26.5 DEG C; Intensity of illumination is 800-2000Lux;Artemia culture initial density is 8/ml.Raised with Isochrysis galbana before artemia pseudimago Support, consumption is:During breeding water body 8L, 8ml after centrifugation, three times a day timing bait throwing in;Raised with grouper in the artemia pseudimago phase Material is raised, and consumption is:During breeding water body 8L, pulverize last 1g, twice a day timing bait throwing in.In the adult stage, with grouper Fermented feed is raised, and each consumption is:During breeding water body 8L, 12ml, twice a day timing bait throwing in;
Also added with Fe-EDTA concentration for 15mg/L is simultaneously 5mg/L using trehalose concentration in adult stage water body.
Any medicine group no added compared to the same period, egg laying rate of red swamp increased 40.4%.

Claims (5)

1. a kind of method that man-made drugs' control produces Artemia cysts, it is characterised in that as follows including step:
(1) configuration of Artemia cysts seawater:Running water adds sodium hypochlorite to be aerated 24 hours, adds sea crystal to be configured to salt afterwards The artificial sea water for 20 ‰ -60 ‰ is spent, aeration is then proceeded to 24 hours, controls the pH of seawater between 7.5-8.5, seawater is molten The concentration of oxygen is solved between 4mg/L---6mg/L, water temperature is between 24.5-26.5 DEG C;
(2) hatching of artemia nauplii:The Artemia cysts that will be bought are put into the seawater for having configured, and deliver density for 1L matches somebody with somebody The seawater put adds 1g Artemia cysts, while adding 1g sodium acid carbonates, brooding time to keep illumination during being 24h, hatching Intensity is put on to 28 DEG C water temperature between 1000-2000Lux, keeps constantly inflation preventing and treating artemia cysts to sink during hatching Bottom, resting egg hatches into artemia nauplii completely after 24h;
(3) nursing of artemia nauplii and pseudimago early stage,
1. the human configuration sea conditions for cultivating be pH between 7.5-8.5, dissolved oxygen concentration be maintained at 4mg/L-6mg/L it Between, water temperature is maintained between 24.5 DEG C -26.5 DEG C;Intensity of illumination is maintained between 800-2000Lux;
2. cultivation density is 7-10/ml;
3. breeding bait and injected volume:
A. after artemia hatching within 24 hours without feeding, during the nauplius of-the five day second day, raised with Isochrysis galbana Support, each consumption is:During breeding water body 1L, the Isochrysis galbana 1ml after centrifugation, three times a day timing bait throwing in;
B. after nauplius during the pseudimago of-the ten day the 6th day, raised with epinephelus feed, each consumption is:Cultivation water During body 8L, epinephelus feed is pulverized last 0.5g, is fed at twice daily;
(4) artemia imago is fed and is hatched,
1. the seawater that will be configured during above-mentioned artemia nauplii and pseudimago keep intensity of illumination 800-2000Lux it Between;
2. breeding bait and injected volume:Raised with grouper fermented feed, each consumption of grouper fermented feed is:Breeding water body During 8L, each feeding volume is 12ml, twice a day timing bait throwing in;
3. in whole adult breeding process, Fe-EDTA is added in the seawater of above-mentioned cultivation, concentration reaches in making seawater 15mg-45mg/L, or trehalose is added, concentration reaches 5mg-15mg/L in making seawater, or adds Fe-EDTA simultaneously, makes seawater Middle concentration reaches 15mg-45mg/L and adds trehalose, and concentration reaches 5mg-15mg/L in making seawater, and cultivation is opened after 12 days or so Begin to lay eggs, the yield of Artemia cysts reaches more than 60%.
2. the method that man-made drugs' control according to claim 1 produces Artemia cysts, it is characterised in that:The step (3) the B step nursing processes 3. walked in, and before being fed every time during the artemia imago of (4) step is fed, to carry out cleaning residual Bait and excrement.
3. the method that man-made drugs' control according to claim 1 produces Artemia cysts, it is characterised in that:The step (3) the grouper fermented feed 2. walked in specifically includes the following component constituted by mass fraction:1 part of brown sugar, epinephelus feed 0.5 part of 20 parts, 500 parts of distilled water, 15 parts of sodium chloride and bacillus powder are after said mixture is aerated 4 hours then close through 30 DEG C Seal ferment 24 hours, wherein epinephelus feed is bought by market.
4. the method that man-made drugs' control according to claim 1 produces Artemia cysts, it is characterised in that:It is described all The optimum salinity of the artificial seawater of step is 30 ‰.
5. the method that man-made drugs' control according to claim 1 produces Artemia cysts, it is characterised in that:The step (4) optimal Fe-EDTA additions are that concentration reaches 30mg/L in making seawater in 3. step;Optimal trehalose addition is to make Concentration reaches 10mg/L in seawater.
CN201611069293.4A 2016-11-29 2016-11-29 A kind of method that man-made drugs' control produces Artemia cysts Withdrawn CN106719442A (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109618990A (en) * 2018-12-04 2019-04-16 天津海友佳音生物科技股份有限公司 A kind of incubation fluid and its hatching method of high density shelling slag oxygenation
CN111289703A (en) * 2020-04-14 2020-06-16 同济大学 Method for testing ecological toxicity of disinfection by-product
CN114698600A (en) * 2022-03-28 2022-07-05 浙江省淡水水产研究所 Method for efficiently purifying artemia used in shrimp seedling raising period

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109618990A (en) * 2018-12-04 2019-04-16 天津海友佳音生物科技股份有限公司 A kind of incubation fluid and its hatching method of high density shelling slag oxygenation
CN111289703A (en) * 2020-04-14 2020-06-16 同济大学 Method for testing ecological toxicity of disinfection by-product
CN114698600A (en) * 2022-03-28 2022-07-05 浙江省淡水水产研究所 Method for efficiently purifying artemia used in shrimp seedling raising period

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Application publication date: 20170531