CN107223636A - Efficient Tiny ecosystem maggot culturing method - Google Patents
Efficient Tiny ecosystem maggot culturing method Download PDFInfo
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- CN107223636A CN107223636A CN201710488591.5A CN201710488591A CN107223636A CN 107223636 A CN107223636 A CN 107223636A CN 201710488591 A CN201710488591 A CN 201710488591A CN 107223636 A CN107223636 A CN 107223636A
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- 238000000034 method Methods 0.000 title claims abstract description 23
- 238000012258 culturing Methods 0.000 title claims abstract description 13
- 238000009395 breeding Methods 0.000 claims abstract description 21
- 230000001488 breeding effect Effects 0.000 claims abstract description 21
- 241000304160 Sarcophaga carnaria Species 0.000 claims abstract description 19
- 241000255581 Drosophila <fruit fly, genus> Species 0.000 claims abstract description 17
- 230000013011 mating Effects 0.000 claims abstract description 7
- 241000255925 Diptera Species 0.000 claims abstract description 6
- 241000382353 Pupa Species 0.000 claims description 25
- 235000015097 nutrients Nutrition 0.000 claims description 18
- 241000894006 Bacteria Species 0.000 claims description 6
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- ZKQDCIXGCQPQNV-UHFFFAOYSA-N Calcium hypochlorite Chemical compound [Ca+2].Cl[O-].Cl[O-] ZKQDCIXGCQPQNV-UHFFFAOYSA-N 0.000 claims description 4
- 230000015572 biosynthetic process Effects 0.000 claims description 4
- 239000007844 bleaching agent Substances 0.000 claims description 4
- 239000004744 fabric Substances 0.000 claims description 4
- 239000011521 glass Substances 0.000 claims description 4
- 235000016709 nutrition Nutrition 0.000 claims description 4
- 238000012216 screening Methods 0.000 claims description 4
- 241000193830 Bacillus <bacterium> Species 0.000 claims description 3
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 claims description 3
- BUGBHKTXTAQXES-UHFFFAOYSA-N Selenium Chemical compound [Se] BUGBHKTXTAQXES-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 239000011651 chromium Substances 0.000 claims description 3
- 229910052804 chromium Inorganic materials 0.000 claims description 3
- 229910052732 germanium Inorganic materials 0.000 claims description 3
- GNPVGFCGXDBREM-UHFFFAOYSA-N germanium atom Chemical compound [Ge] GNPVGFCGXDBREM-UHFFFAOYSA-N 0.000 claims description 3
- 235000014655 lactic acid Nutrition 0.000 claims description 3
- 239000004310 lactic acid Substances 0.000 claims description 3
- 230000000243 photosynthetic effect Effects 0.000 claims description 3
- 239000011669 selenium Substances 0.000 claims description 3
- 229910052711 selenium Inorganic materials 0.000 claims description 3
- 239000011701 zinc Substances 0.000 claims description 3
- 229910052725 zinc Inorganic materials 0.000 claims description 3
- 239000005996 Blood meal Substances 0.000 claims description 2
- 235000019733 Fish meal Nutrition 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- 235000010627 Phaseolus vulgaris Nutrition 0.000 claims description 2
- 244000046052 Phaseolus vulgaris Species 0.000 claims description 2
- 239000004467 fishmeal Substances 0.000 claims description 2
- 244000005700 microbiome Species 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 2
- 241000255588 Tephritidae Species 0.000 claims 1
- 102000004169 proteins and genes Human genes 0.000 abstract description 4
- 108090000623 proteins and genes Proteins 0.000 abstract description 4
- 230000001850 reproductive effect Effects 0.000 abstract description 4
- 241000196324 Embryophyta Species 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 241000202814 Cochliomyia hominivorax Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- ZPEIMTDSQAKGNT-UHFFFAOYSA-N chlorpromazine Chemical compound C1=C(Cl)C=C2N(CCCN(C)C)C3=CC=CC=C3SC2=C1 ZPEIMTDSQAKGNT-UHFFFAOYSA-N 0.000 description 1
- 238000013461 design Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01K—ANIMAL HUSBANDRY; AVICULTURE; APICULTURE; PISCICULTURE; FISHING; REARING OR BREEDING ANIMALS, NOT OTHERWISE PROVIDED FOR; NEW BREEDS OF ANIMALS
- A01K67/00—Rearing or breeding animals, not otherwise provided for; New or modified breeds of animals
- A01K67/033—Rearing or breeding invertebrates; New breeds of invertebrates
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Environmental Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Zoology (AREA)
- Animal Husbandry (AREA)
- Biodiversity & Conservation Biology (AREA)
- Fodder In General (AREA)
Abstract
A kind of efficient Tiny ecosystem maggot culturing method, is related to fly maggot breeding technical field, this method comprises the following steps：Step 1: breeding, first selection flesh fly, drosophila, calliphorid and each 4 of tachinid, first choice chooses a flesh fly and with a drosophila mate obtaining fly maggot A, take a calliphorid to be mated with a tachinid again and obtain fly maggot B, take a flesh fly to be mated with a calliphorid and obtain fly maggot C, this method passes through breeding, a variety of flies are mated, classic engineering fly is obtained during mating, utilizing works fly carries out seed selection breeding, the reproductive efficiency of fly maggot can be made higher, simultaneously the figure of fly maggot can be made fuller, protein more enriches.
Description
Technical field：
The present invention relates to fly maggot breeding technical field, and in particular to a kind of efficient Tiny ecosystem maggot culturing method.
Background technology：
Fly maggot is screwworm.Mainly multiply in human and animal excreta heap, rubbish, corrupt substance, take food excrement and rot
Material, what is also had moves in corrupt spoil.Pupate, survived the winter with pupa under native table, hibernal pupae in soil depth up to 10
Cm.Fly-maggot protein matter is high quality white, is not only high-quality feed, also can extract albumen powder, exploitation senior nutrition, space flight
Food, medicine, the breeding way of existing fly maggot are also only limited to the cultivation of traditional approach, although during cultivation
Substantial amounts of fly maggot can be obtained, but the content that such a fly maggot contains protein is relatively low, it is impossible to needed for meeting people, therefore for upper
Technical problem is stated, spy proposes a kind of new technical scheme.
The content of the invention：
The invention aims to overcome the weak point that above-mentioned prior art is present, and provide a kind of efficient Tiny ecosystem
Maggot culturing method.
The technical solution adopted by the present invention is：A kind of efficient Tiny ecosystem maggot culturing method, this method comprises the following steps：
Step 1: breeding, first selection flesh fly, drosophila, calliphorid and each 4 of tachinid, first choice choose a flesh fly and one
Drosophila mate obtaining fly maggot A, then takes a calliphorid to mate with a tachinid to obtain fly maggot B, take a flesh fly and one
The mating of calliphorid obtains fly maggot C, takes a flesh fly to be mated with a tachinid and obtains fly maggot D, takes a drosophila to be mated with calliphorid
Obtain fly maggot E, take a drosophila to be mated with tachinid and obtain fly maggot F, then respectively by fly maggot A, fly maggot B, fly maggot C, fly maggot D,
Fly maggot E and fly maggot F are raised, and allow it to become adult flies worm, and the fly worm that the fly worm produced by fly maggot A is produced with fly maggot B is handed over
With fly maggot G is obtained, the fly worm produced by fly maggot C mate obtaining fly maggot H with the fly worm that fly maggot D is produced, will be by fly maggot volume
The fly worm of generation mate obtaining fly maggot I with the fly worm that fly maggot F is produced, and the fly worm produced by fly maggot G and fly maggot H are produced
Fly worm mate obtaining fly maggot J, and the fly worm produced by fly maggot J mate obtaining fly maggot K with the fly worm that fly maggot I is produced,
It is engineering fly by the fly worm that fly maggot K carries out live box formation；
Step 2: seed selection, a kind of engineering fly of step is raised in fly cage, fly cage is cylinder, the ground of cylinder
A diameter of 80cm, the height of cylinder is to hang with the grid cloth with circular port on 160cm, cylinder, and the diameter of circular port is not
More than 2cm, the bottom or top of cylinder, which are provided with, is put into mouth；Engineering fly pupa in fly cage is allowed, after being soaked after pupa with bleaching powder
2min is steeped, selection length is no less than 3cm, and diameter is no less than 1cm pupa, and the select tools of pupa diameter are screening washer, and will selection
Good pupa, which is placed into fly cage B, is raised, and fly cage is placed in the environment that temperature is 20-35 DEG C, humidity is 90%；In fly
One glass of nutrient solution is placed in cage B, the volume of nutrient solution is 15ml, while placing 10g bait, bait is placed in bait disc
Portion；
Step 3: breeding, the pupa in the fly cage B in step 2 being raised and bred, its quantity is allowed to be increased,
Fly maggot is taken out from fly cage B after quantity increase, and be will move in bigger fly cage, while being 35- by the temperature of fly cage
40 DEG C, humidity for 95% environment in, while placing substantial amounts of nutrient solution and bait wherein, the fly cage allowed in large space is obtained
Quick breeding.
Described nutrient solution is mixed by photosynthetic bacteria, bacillus and lactic acid bacteria, and two are at least during mixing
Plant the mixture of the above.
Described nutrient solution is mixed by selenium, germanium, chromium, five kinds of life nutritional elements of zinc and calcium, during mixing
At least two or more mixtures.
Described bait is mixed by rice bran, blood meal, fish meal, bean dregs, effective microorganisms(EM) and water.
Beneficial effects of the present invention are：This method is mated a variety of flies by breeding, in the process of mating
In obtain classic engineering fly, utilizing works fly carries out seed selection breeding, the reproductive efficiency of fly maggot can be made higher, while can
Make the figure of fly maggot fuller, protein more enriches.
Embodiment：
The present invention is further described in conjunction with specific embodiments：
Embodiment one：
A kind of efficient Tiny ecosystem maggot culturing method, it is characterised in that：This method comprises the following steps：
Step 1: breeding, first selection flesh fly, drosophila, calliphorid and each 4 of tachinid, first choice choose a flesh fly and one
Drosophila mate obtaining fly maggot A, then takes a calliphorid to mate with a tachinid to obtain fly maggot B, take a flesh fly and one
The mating of calliphorid obtains fly maggot C, takes a flesh fly to be mated with a tachinid and obtains fly maggot D, takes a drosophila to be mated with calliphorid
Obtain fly maggot E, take a drosophila to be mated with tachinid and obtain fly maggot F, then respectively by fly maggot A, fly maggot B, fly maggot C, fly maggot D,
Fly maggot E and fly maggot F are raised, and allow it to become adult flies worm, and the fly worm that the fly worm produced by fly maggot A is produced with fly maggot B is handed over
With fly maggot G is obtained, the fly worm produced by fly maggot C mate obtaining fly maggot H with the fly worm that fly maggot D is produced, will be by fly maggot volume
The fly worm of generation mate obtaining fly maggot I with the fly worm that fly maggot F is produced, and the fly worm produced by fly maggot G and fly maggot H are produced
Fly worm mate obtaining fly maggot J, and the fly worm produced by fly maggot J mate obtaining fly maggot K with the fly worm that fly maggot I is produced,
It is engineering fly by the fly worm that fly maggot K carries out live box formation；
Step 2: seed selection, a kind of engineering fly of step is raised in fly cage, fly cage is cylinder, the ground of cylinder
A diameter of 80cm, the height of cylinder is to hang with the grid cloth with circular port on 160cm, cylinder, and the diameter of circular port is not
More than 2cm, the bottom or top of cylinder, which are provided with, is put into mouth；Engineering fly pupa in fly cage is allowed, after being soaked after pupa with bleaching powder
2min is steeped, selection length is no less than 3cm, and diameter is no less than 1cm pupa, and the select tools of pupa diameter are screening washer, and will selection
Good pupa, which is placed into fly cage B, is raised, and fly cage is placed in the environment that temperature is 35 DEG C, humidity is 90%；In fly cage B
One glass of nutrient solution of interior placement, the volume of nutrient solution is 15ml, while placing 10g bait, bait is placed on inside bait disc；
Step 3: breeding, the pupa in the fly cage B in step 2 being raised and bred, its quantity is allowed to be increased,
Fly maggot is taken out from fly cage B after quantity increase, and be will move in bigger fly cage, while being 40 by the temperature of fly cage
DEG C, humidity for 95% environment in, while placing substantial amounts of nutrient solution and bait wherein, the fly cage allowed in large space is obtained soon
Speed breeding.
Described nutrient solution is mixed by photosynthetic bacteria, bacillus and lactic acid bacteria, and two are at least during mixing
Plant the mixture of the above.
Embodiment two：
A kind of efficient Tiny ecosystem maggot culturing method, this method comprises the following steps：
Step 1: breeding, first selection flesh fly, drosophila, calliphorid and each 4 of tachinid, first choice choose a flesh fly and one
Drosophila mate obtaining fly maggot A, then takes a calliphorid to mate with a tachinid to obtain fly maggot B, take a flesh fly and one
The mating of calliphorid obtains fly maggot C, takes a flesh fly to be mated with a tachinid and obtains fly maggot D, takes a drosophila to be mated with calliphorid
Obtain fly maggot E, take a drosophila to be mated with tachinid and obtain fly maggot F, then respectively by fly maggot A, fly maggot B, fly maggot C, fly maggot D,
Fly maggot E and fly maggot F are raised, and allow it to become adult flies worm, and the fly worm that the fly worm produced by fly maggot A is produced with fly maggot B is handed over
With fly maggot G is obtained, the fly worm produced by fly maggot C mate obtaining fly maggot H with the fly worm that fly maggot D is produced, will be by fly maggot volume
The fly worm of generation mate obtaining fly maggot I with the fly worm that fly maggot F is produced, and the fly worm produced by fly maggot G and fly maggot H are produced
Fly worm mate obtaining fly maggot J, and the fly worm produced by fly maggot J mate obtaining fly maggot K with the fly worm that fly maggot I is produced,
It is engineering fly by the fly worm that fly maggot K carries out live box formation；
Step 2: seed selection, a kind of engineering fly of step is raised in fly cage, fly cage is cylinder, the ground of cylinder
A diameter of 80cm, the height of cylinder is to hang with the grid cloth with circular port on 160cm, cylinder, and the diameter of circular port is not
More than 2cm, the bottom or top of cylinder, which are provided with, is put into mouth；Engineering fly pupa in fly cage is allowed, after being soaked after pupa with bleaching powder
2min is steeped, selection length is no less than 3cm, and diameter is no less than 1cm pupa, and the select tools of pupa diameter are screening washer, and will selection
Good pupa, which is placed into fly cage B, is raised, and fly cage is placed in the environment that temperature is 35 DEG C, humidity is 90%；In fly cage B
One glass of nutrient solution of interior placement, the volume of nutrient solution is 15ml, while placing 10g bait, bait is placed on inside bait disc；
Step 3: breeding, the pupa in the fly cage B in step 2 being raised and bred, its quantity is allowed to be increased,
Fly maggot is taken out from fly cage B after quantity increase, and be will move in bigger fly cage, while being 40 by the temperature of fly cage
DEG C, humidity for 95% environment in, while placing substantial amounts of nutrient solution and bait wherein, the fly cage allowed in large space is obtained soon
Speed breeding.
Described nutrient solution is mixed by selenium, germanium, chromium, five kinds of life nutritional elements of zinc and calcium, during mixing
At least two or more mixtures.
Using effect is tested：
This research is continuously on probation 1 year by 100 enterprises, investigates the effect of the efficient Tiny ecosystem maggot culturing method each side
Really.Test event standards of grading are：Very satisfied 5 points, 4 points are satisfied with, general 3 points, 2 points, very dissatisfied 1 point are unsatisfied with.Its
In common group be conventional ceramic base substrate reinforcing agent；
| Test event | Embodiment one | Embodiment two | Common group |
| Fly maggot build | 4.8 | 4.9 | 3.0 |
| Protein content | 4.8 | 4.9 | 1.0 |
| Growth rate | 4.7 | 4.9 | 3.0 |
| Reproductive number | 4.7 | 4.9 | 3.0 |
In summary, the fly maggot for cultivating out using the method has build big, and protein content is high, and reproductive number is more,
The fast advantage of growth rate, the drawbacks of can solving to bring in traditional breeding process significantly, to user bring convenience it is same
When, moreover it is possible to it is improved economic benefit.
For those skilled in the art, other can be made various corresponding according to above technical scheme and design
Change and deformation, and all these change and deformation should all belong within the protection domain of the claims in the present invention.
Claims (4)
1. a kind of efficient Tiny ecosystem maggot culturing method, it is characterised in that：This method comprises the following steps：
Step 1: breeding, first selection flesh fly, drosophila, calliphorid and each 4 of tachinid, first choice choose a flesh fly and a fruit
Fly mate and obtains fly maggot A, then takes a calliphorid to mate with a tachinid to obtain fly maggot B, take a flesh fly and one it is beautiful
Fly mating obtains fly maggot C, takes a flesh fly to be mated with a tachinid and obtains fly maggot D, takes a drosophila to be mated with calliphorid and obtain
Fly maggot E, takes a drosophila to be mated with tachinid and obtains fly maggot F, then respectively by fly maggot A, fly maggot B, fly maggot C, fly maggot D, fly maggot E
And fly maggot F is raised, allow it to become adult flies worm, the fly worm produced by fly maggot A is mated with the fly worm that fly maggot B is produced
Fly maggot G, the fly worm produced by fly maggot C mate obtaining fly maggot H with the fly worm that fly maggot D is produced, by what is produced by fly maggot volume
Fly worm mate obtaining fly maggot I with the fly worm that fly maggot F is produced, and the fly worm that the fly worm produced by fly maggot G is produced with fly maggot H enters
Row mating obtains fly maggot J, the fly worm produced by fly maggot J mate obtaining fly maggot K with the fly worm that fly maggot I is produced, by fly maggot K
The fly worm for carrying out live box formation is engineering fly；
Step 2: seed selection, a kind of engineering fly of step is raised in fly cage, fly cage is cylinder, the Ground Diameter of cylinder
For 80cm, the height of cylinder is to hang with the grid cloth with circular port on 160cm, cylinder, and the diameter of circular port is not more than
2cm, the bottom or top of cylinder, which are provided with, is put into mouth；Engineering fly pupa in fly cage is allowed, after being soaked after pupa with bleaching powder
2min, selection length is no less than 3cm, and diameter is no less than 1cm pupa, and the select tools of pupa diameter are screening washer, and will be chosen
Pupa be placed into fly cage B and raised, fly cage is placed in the environment that temperature is 20-35 DEG C, humidity is 90%；In fly cage
One glass of nutrient solution is placed in B, the volume of nutrient solution is 15ml, while placing 10g bait, bait is placed on inside bait disc；
Step 3: breeding, the pupa in the fly cage B in step 2 being raised and bred, its quantity is allowed to be increased, in quantity
Fly maggot is taken out from fly cage B after increase, and be will move in bigger fly cage, while be 35-40 DEG C by the temperature of fly cage,
Humidity is in 95% environment, while placing substantial amounts of nutrient solution and bait wherein, the fly cage allowed in large space obtains quickly
Breeding.
2. efficient Tiny ecosystem maggot culturing method according to claim 1, it is characterised in that：Described nutrient solution is by photosynthetic
Bacterium, bacillus and lactic acid bacteria are mixed, and two or more mixtures are at least during mixing.
3. efficient Tiny ecosystem maggot culturing method according to claim 1, it is characterised in that：Described nutrient solution by selenium,
Germanium, chromium, five kinds of life nutritional elements of zinc and calcium are mixed, and two or more mixtures are at least during mixing.
4. efficient Tiny ecosystem maggot culturing method according to claim 1, it is characterised in that：Described bait by rice bran,
Blood meal, fish meal, bean dregs, effective microorganisms(EM) and water are mixed.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710488591.5A CN107223636A (en) | 2017-06-23 | 2017-06-23 | Efficient Tiny ecosystem maggot culturing method |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CN201710488591.5A CN107223636A (en) | 2017-06-23 | 2017-06-23 | Efficient Tiny ecosystem maggot culturing method |
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Family
ID=59936175
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| Application Number | Title | Priority Date | Filing Date |
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| CN201710488591.5A Pending CN107223636A (en) | 2017-06-23 | 2017-06-23 | Efficient Tiny ecosystem maggot culturing method |
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Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1528137A (en) * | 2003-10-21 | 2004-09-15 | 邢荣山 | Herbivorous housefly and fly maggot breeding method |
| CN102389034A (en) * | 2011-08-29 | 2012-03-28 | 常先苗 | Preparation method of bait for culturing maggot |
| CN104621050A (en) * | 2015-02-11 | 2015-05-20 | 天津林鹤生物科技有限公司 | Food chain culturing method of maggots and earthworms |
-
2017
- 2017-06-23 CN CN201710488591.5A patent/CN107223636A/en active Pending
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1528137A (en) * | 2003-10-21 | 2004-09-15 | 邢荣山 | Herbivorous housefly and fly maggot breeding method |
| CN102389034A (en) * | 2011-08-29 | 2012-03-28 | 常先苗 | Preparation method of bait for culturing maggot |
| CN104621050A (en) * | 2015-02-11 | 2015-05-20 | 天津林鹤生物科技有限公司 | Food chain culturing method of maggots and earthworms |
Non-Patent Citations (2)
| Title |
|---|
| 赵子瑞: "三元杂交蝇蛆简易养殖", 《农村养殖技术》 * |
| 鲍根良: "优质动物高蛋白无菌蝇蛆的生产技术", 《农牧产品开发》 * |
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