CN102627489A - Cultivated formula for white Hypsizigus marmoreus and preparation method thereof - Google Patents
Cultivated formula for white Hypsizigus marmoreus and preparation method thereof Download PDFInfo
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- CN102627489A CN102627489A CN2012100818868A CN201210081886A CN102627489A CN 102627489 A CN102627489 A CN 102627489A CN 2012100818868 A CN2012100818868 A CN 2012100818868A CN 201210081886 A CN201210081886 A CN 201210081886A CN 102627489 A CN102627489 A CN 102627489A
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
- Y02A40/20—Fertilizers of biological origin, e.g. guano or fertilizers made from animal corpses
Abstract
The invention discloses a cultivated formula for white Hypsizigus marmoreus and a preparation method thereof. The cultivated formula is prepared from cottonseed hull, cob, dry pig manure slag, corn flour, wood chip, lime and light calcium carbonate. The preparation method is as below: (1) first pouring the pig manure into a solid-liquid separator for solid-liquid separation to obtain pig manure slag, and then drying the pig manure slag in the sun to obtain dry pig manure slag; (2) adding water into cottonseed hull, cob, dry pig manure slag, corn flour, wood chip, lime and light calcium carbonate, stirring and packaging the mixture; (3) disinfecting the mixture at normal pressure for 16 h; (4) carrying out inoculation in a sterile room after the fungus bag cooling to 15-18 DEG C; (5) transferring the fungus bag to a culture room for fungus cultivation; (6) carrying out fungus scratching; and (7) propagating the fungus. The cultivated formula has advantages of substituting wheat bran, changing waste into valuables and reducing environmental pollution, etc.
Description
Technical field
The present invention relates to a kind of edible fungus culturing raw material, relate in particular to a kind of white Hypsizygus marmoreus cultivation prescription.The invention still further relates to the preparation method of this white Hypsizygus marmoreus cultivation prescription.
Background technology
Chinese patent CN101580425A discloses a kind of like this compound method of Hypsizigus marmoreus compost, comprises wood chip 32～45%, wheat bran 25～40%, corn cob 12～19%, Semen Maydis powder 3.6～6.7%, rice Icing Sugar 3.5～4%, Wheat Straw powder 0.5～1%, white sugar 1.7～2%, lime 0.5～1%, gypsum 0.1～0.3%, crosses dahllite 0.1～0.3%, brown sugar 0.1～0.3%, sal epsom 0.5～0.8%.Chinese patent CN101684054A also discloses a kind of like this high yield beech mushrooms and has joined foster prescription, comprises wood chip 5～15%, wheat bran 7～23%, corn cob 20～35%, cotton seed hulls 5～20%, soybean 5～20%, rice sugar 20～35%, Semen Maydis powder 2～10%, lime 0.1～1%.Such scheme has all adopted wheat bran as culturing raw material, and its production cost is higher.Along with economy constantly develops; People's living standard is improved constantly; Pig-breeding also obtains large development, simultaneously, in the pig-breeding process, can produce a large amount of pig manures; Cause severe environmental pollution, the pollution of how turning waste into wealth, reducing environment is the task of top priority of aquaculture Sustainable development.
Summary of the invention
The purpose of this invention is to provide a kind of ability and substitute wheat bran, and turn waste into wealth, reduce white Hypsizygus marmoreus cultivation prescription of environmental pollution and preparation method thereof.
For achieving the above object, the present invention's white Hypsizygus marmoreus cultivation prescription is characterized in that it is to be processed by the following weight proportion raw material
Cotton seed hulls 25～35% corn cobs 10～20% dried pig manure slag 23～30% Semen Maydis powder 3～7% wood chips 17～24% lime 1.0～3.0% light calcium carbonates 0.5～1.5%.
Wherein the proportioning of each raw material weight is
Cotton seed hulls 30% corn cob 15% dried pig manure slag 26% Semen Maydis powder 5% wood chip 21% lime 2.0% light calcium carbonate 1%.
The preparation method of white Hypsizygus marmoreus cultivation prescription comprises
Pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtaining water cut is the dried pig manure slag of 13-15%.
(1) pack: earlier cotton seed hulls, corn cob, dried pig manure slag, Semen Maydis powder, wood chip, lime, light calcium carbonate above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed, its water cut is 60～65%,
(2) sterilization: normal-pressure sterilization 100 degree kept 16 hours,
(3) inoculation: treat that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending,
(4) bacteria: change culturing room after having inoculated over to and carry out bacteria, 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days,
(5) mycelium stimulation: will cultivate the aerial hyphae on bag surface, and take off with two teeth and remove old clumping of over grown hyphae in surface and aerial hyphae, the aerial hyphae layer is also left on the surface of cultivation bag,
(6) fertility: the cultivation bag that will open behind the bag moves into, and is emitted on a cultivation layer frame, between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align; Be convenient to convection of air between the levels, enough developmenting spaces arranged after making new mushroom bud fruiting, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
The present invention has following advantage: because pig manure is a kind of source of manure that is rich in organism and nitrogen phosphorus potassium; Substitute wheat bran as one of white Hypsizygus marmoreus cultivation with pig manure; Not only solve the pig manure problem of environment pollution caused, also saved the production cost that white Hypsizygus marmoreus is produced in batch production.White Hypsizygus marmoreus culture cycle shortens to 80 days by 90 days of routine techniques, shortens 11.11% incubation time, reduces production costs, and every bag reduces cost 0.1 yuan.
EmbodimentBelow in conjunction with embodiment, the present invention is done to describe further.
Embodiment one
Earlier pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtain water cut and be 13% dried pig manure slag.Then, cotton seed hulls 25%, corn cob 13%, dried pig manure slag 30%, Semen Maydis powder 5.5%, wood chip 24%, lime 1.0%, light calcium carbonate 1.5% above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed; Its water cut is 60%, and normal-pressure sterilization 100 degree kept 16 hours, treats that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending, and changes culturing room over to after having inoculated and carries out bacteria; 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days, with the aerial hyphae on cultivation bag surface, take off with two teeth and to remove surperficial old clumping of over grown hyphae and aerial hyphae; The aerial hyphae layer is also left on the surface of cultivation bag, and the cultivation bag of opening behind the bag is moved into, and is emitted on a cultivation layer frame; Between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align, be convenient to convection of air between the levels; After making new mushroom bud fruiting enough developmenting spaces are arranged, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
Embodiment two
Earlier pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtain water cut and be 15% dried pig manure slag.Then, cotton seed hulls 30% corn cob 15% dried pig manure slag 26% Semen Maydis powder 5% wood chip 21% lime 2.0% light calcium carbonate 1% above-mentioned materials is added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed; Its water cut is 61%, and normal-pressure sterilization 100 degree kept 16 hours, treats that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending, and changes culturing room over to after having inoculated and carries out bacteria; 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days, with the aerial hyphae on cultivation bag surface, take off with two teeth and to remove surperficial old clumping of over grown hyphae and aerial hyphae; The aerial hyphae layer is also left on the surface of cultivation bag, and the cultivation bag of opening behind the bag is moved into, and is emitted on a cultivation layer frame; Between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align, be convenient to convection of air between the levels; After making new mushroom bud fruiting enough developmenting spaces are arranged, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
Embodiment three
Earlier pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtain water cut and be 14% dried pig manure slag.Then, cotton seed hulls 35%, corn cob 18.5%, dried pig manure slag 23%, Semen Maydis powder 3%, wood chip 17%, lime 3%, light calcium carbonate 0.5% above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed; Its water cut is 62%, and normal-pressure sterilization 100 degree kept 16 hours, treats that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending, and changes culturing room over to after having inoculated and carries out bacteria; 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days, with the aerial hyphae on cultivation bag surface, take off with two teeth and to remove surperficial old clumping of over grown hyphae and aerial hyphae; The aerial hyphae layer is also left on the surface of cultivation bag, and the cultivation bag of opening behind the bag is moved into, and is emitted on a cultivation layer frame; Between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align, be convenient to convection of air between the levels; After making new mushroom bud fruiting enough developmenting spaces are arranged, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
Embodiment four
Earlier pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtain water cut and be 13% dried pig manure slag.Then, cotton seed hulls 26%, corn cob 20%, dried pig manure slag 25%, Semen Maydis powder 7%, wood chip 19.5%, lime 1.0%, light calcium carbonate 1.5% above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed; Its water cut is 63%, and normal-pressure sterilization 100 degree kept 16 hours, treats that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending, and changes culturing room over to after having inoculated and carries out bacteria; 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days, with the aerial hyphae on cultivation bag surface, take off with two teeth and to remove surperficial old clumping of over grown hyphae and aerial hyphae; The aerial hyphae layer is also left on the surface of cultivation bag, and the cultivation bag of opening behind the bag is moved into, and is emitted on a cultivation layer frame; Between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align, be convenient to convection of air between the levels; After making new mushroom bud fruiting enough developmenting spaces are arranged, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
Embodiment five
Earlier pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtain water cut and be 15% dried pig manure slag.Then, cotton seed hulls 33%, corn cob 10%, dried pig manure slag 28%, Semen Maydis powder 4%, wood chip 21%, lime 2.5%, light calcium carbonate 1.5% above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed; Its water cut is 65%, and normal-pressure sterilization 100 degree kept 16 hours, treats that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending, and changes culturing room over to after having inoculated and carries out bacteria; 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days, with the aerial hyphae on cultivation bag surface, take off with two teeth and to remove surperficial old clumping of over grown hyphae and aerial hyphae; The aerial hyphae layer is also left on the surface of cultivation bag, and the cultivation bag of opening behind the bag is moved into, and is emitted on a cultivation layer frame; Between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align, be convenient to convection of air between the levels; After making new mushroom bud fruiting enough developmenting spaces are arranged, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days.
Claims (3)
1. a white Hypsizygus marmoreus cultivation prescription is characterized in that it is to be processed by the following weight proportion raw material
Cotton seed hulls 25～35% corn cobs 10～20% dried pig manure slag 23～30% Semen Maydis powder 3～7% wood chips 17～24% lime 1.0～3.0% light calcium carbonates 0.5～1.5%.
2. white Hypsizygus marmoreus cultivation prescription according to claim 1, wherein the proportioning of each raw material weight is
Cotton seed hulls 30% corn cob 15% dried pig manure slag 26% Semen Maydis powder 5% wood chip 21% lime 2.0% light calcium carbonate 1%.
3. the preparation method of white Hypsizygus marmoreus cultivation prescription according to claim 1 comprises
(1) pack: earlier cotton seed hulls, corn cob, dried pig manure slag, Semen Maydis powder, wood chip, lime, light calcium carbonate above-mentioned materials are added water stirring pack after 45 minutes, the packed 17cm of the propylene of 17*33, every bag of heavy 1.0kg of wet feed, its water cut is 60～65%,
(2) sterilization: normal-pressure sterilization 100 degree kept 16 hours,
(3) inoculation: treat that bacterium bag temperature drops to 15～18 and inoculates at sterilisable chamber when spending,
(4) bacteria: change culturing room after having inoculated over to and carry out bacteria, 60 days cultivation initial stages remained on 21～23 degree, after rise to 23～25 degree and continue to cultivate 20～30 days,
(5) mycelium stimulation: will cultivate the aerial hyphae on bag surface, and take off with two teeth and remove old clumping of over grown hyphae in surface and aerial hyphae, the aerial hyphae layer is also left on the surface of cultivation bag,
(6) fertility: the cultivation bag that will open behind the bag moves into, and is emitted on a cultivation layer frame, between the cultivation bag spacing 1-2 centimetre, bag with wrap forward and backward, about align; Be convenient to convection of air between the levels, enough developmenting spaces arranged after making new mushroom bud fruiting, sequence bag after, directly use atomizer to spray water to charge level; Spray gun lets droplet directly descend slowly and lightly up, and gradation is sprayed; Roughly 10～20 milliliters of every bag spray water total amounts are opened bag back and are covered and go up woven bag and preserve moisture, and keep relative air humidity 86～92%; Temperature 12～16C, gas concentration lwevel 1000～1500PPM, light nature; Tide over strong mushroom bud after date, heighten gas concentration lwevel to the 4000～5000PPM in the mushroom room, mushroom room, impel mushroom flower bud mushroom handle to elongate fast at once; After tiding over elongating stage, turn down gas concentration lwevel to the 1500～3000PPM in the mushroom room, this purpose is impelled the chap of mushroom handle, and weight increases the weight of; This process is 3～4 days, impels the quick chap of mushroom flower bud mushroom handle; Open behind the bag to the cycle of gathering be 21～23 days, it is characterized in that: pour pig manure into solid-liquid separating machine and carry out solid-liquid separation and obtain the pig manure slag, again the pig manure slag is shone dry-cure, obtaining water cut is the dried pig manure slag of 13-15%.
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Cited By (12)
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| CN102972212A (en) * | 2012-12-28 | 2013-03-20 | 山东省农业科学院农业资源与环境研究所 | Method for producing pleurotus cornucopiae by taking slag powder as cultivation material |
| CN103314788A (en) * | 2013-07-16 | 2013-09-25 | 龚涛 | Practical seafood mushroom culture medium and manufacturing method thereof |
| CN103583232A (en) * | 2013-11-08 | 2014-02-19 | 王尚荣 | Toadstool substrate and cultivation technology of toadstool substrate |
| CN104186203A (en) * | 2014-09-15 | 2014-12-10 | 湖南天扶菇业发展有限公司 | Simplified pleurotus cornucopiae cultivation method |
| CN104247628A (en) * | 2014-09-26 | 2014-12-31 | 陕西省微生物研究所 | Cultivation medium and cultivation method for artificially-cultivated phellinus igniarius |
| CN104429615A (en) * | 2014-12-19 | 2015-03-25 | 苏州市经纬农产品有限公司 | White beech mushroom cultivating method |
| CN104496679A (en) * | 2014-12-19 | 2015-04-08 | 苏州市经纬农产品有限公司 | White beech mushroom culture medium additive |
| CN104945051A (en) * | 2015-06-19 | 2015-09-30 | 桂林健成生物科技开发有限公司 | Application of seed coats/embryonic bodies and rhizomes obtained after harvest of sprout seedling vegetable to cultivation of hypsizigus marmoreus |
| CN105474986A (en) * | 2015-11-25 | 2016-04-13 | 苏州市经纬农产品有限公司 | Method for culturing hypsizygus tessellatus |
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| CN107434569A (en) * | 2016-05-27 | 2017-12-05 | 桂林宏泰养殖农民专业合作社 | A kind of new true pleurotus cornucopiae fuel |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| CN102972212A (en) * | 2012-12-28 | 2013-03-20 | 山东省农业科学院农业资源与环境研究所 | Method for producing pleurotus cornucopiae by taking slag powder as cultivation material |
| CN103314788A (en) * | 2013-07-16 | 2013-09-25 | 龚涛 | Practical seafood mushroom culture medium and manufacturing method thereof |
| CN103314788B (en) * | 2013-07-16 | 2015-12-23 | 汪涛 | A kind of practical seafood mushroom medium and collocation method thereof |
| CN103583232A (en) * | 2013-11-08 | 2014-02-19 | 王尚荣 | Toadstool substrate and cultivation technology of toadstool substrate |
| CN104186203A (en) * | 2014-09-15 | 2014-12-10 | 湖南天扶菇业发展有限公司 | Simplified pleurotus cornucopiae cultivation method |
| CN104247628A (en) * | 2014-09-26 | 2014-12-31 | 陕西省微生物研究所 | Cultivation medium and cultivation method for artificially-cultivated phellinus igniarius |
| CN104496679A (en) * | 2014-12-19 | 2015-04-08 | 苏州市经纬农产品有限公司 | White beech mushroom culture medium additive |
| CN104429615A (en) * | 2014-12-19 | 2015-03-25 | 苏州市经纬农产品有限公司 | White beech mushroom cultivating method |
| CN104945051A (en) * | 2015-06-19 | 2015-09-30 | 桂林健成生物科技开发有限公司 | Application of seed coats/embryonic bodies and rhizomes obtained after harvest of sprout seedling vegetable to cultivation of hypsizigus marmoreus |
| CN106631304A (en) * | 2015-10-31 | 2017-05-10 | 济南健康人药品有限公司 | Method for preparing pleurotus cornucopiae cultivation base by utilizing mixed aquatic plants |
| CN105474986A (en) * | 2015-11-25 | 2016-04-13 | 苏州市经纬农产品有限公司 | Method for culturing hypsizygus tessellatus |
| CN107434569A (en) * | 2016-05-27 | 2017-12-05 | 桂林宏泰养殖农民专业合作社 | A kind of new true pleurotus cornucopiae fuel |
| CN106954462A (en) * | 2017-04-01 | 2017-07-18 | 福建农林大学 | A kind of true pleurotus cornucopiae cultural method |
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