CN105724056A - Planting technologies for pleurotus eryngii and pleurotus geesteranus - Google Patents

Planting technologies for pleurotus eryngii and pleurotus geesteranus Download PDF

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Publication number
CN105724056A
CN105724056A CN201610120006.1A CN201610120006A CN105724056A CN 105724056 A CN105724056 A CN 105724056A CN 201610120006 A CN201610120006 A CN 201610120006A CN 105724056 A CN105724056 A CN 105724056A
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pleurotus eryngii
day
pleurotus
mushroom
compost
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于朋九
祁洪方
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Hebei Zhongwo Agriculture Technology Development Co Ltd
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Hebei Zhongwo Agriculture Technology Development Co Ltd
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    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01GHORTICULTURE; CULTIVATION OF VEGETABLES, FLOWERS, RICE, FRUIT, VINES, HOPS OR SEAWEED; FORESTRY; WATERING
    • A01G18/00Cultivation of mushrooms
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05DINORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
    • C05D3/00Calcareous fertilisers
    • C05D3/02Calcareous fertilisers from limestone, calcium carbonate, calcium hydrate, slaked lime, calcium oxide, waste calcium products
    • CCHEMISTRY; METALLURGY
    • C05FERTILISERS; MANUFACTURE THEREOF
    • C05GMIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
    • C05G3/00Mixtures of one or more fertilisers with additives not having a specially fertilising activity

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  • Life Sciences & Earth Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pest Control & Pesticides (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Mycology (AREA)
  • Environmental Sciences (AREA)
  • Mushroom Cultivation (AREA)

Abstract

The invention relates to planting technologies for pleurotus eryngii and pleurotus geesteranus. The planting technology for the pleurotus eryngii includes the following steps that culture material preparing, sterilization cooling, inoculating, spawn running managing and fruiting managing are performed, wherein a culture material is prepared from, by weight, 20-25 parts of wood chips, 8-12 parts of corn flour, 8-12 parts of bean pulp, 15-20 parts of bran, 30-35 parts of corncobs, 1-2 parts of lime powder and 1-2 parts of calcium carbonate. The technology for the pleurotus geesteranus for planting the pleurotus geesteranus by the utilization of a waste material generated after the pleurotus eryngii is harvested through the planting technology for the pleuritus eryngii includes the steps that culture material preparing, sterilization cooling, inoculating, spawn running managing and fruiting managing are performed; a culture material is prepared form, by weight, 40-45 parts of the pleurotus eryngii waste material, 55-60 parts of cotton seed hulls and 1.5-2.5 parts of lime powder. The technologies are simple, the yield of the pleurotus eryngii is high, and the fruiting period of the pleurotus eryngii is shortened to be eighteen days; the pleurotus eryngii waste material can be utilized for planting the pleurotus geesteranus, in this way, the cost is low, the waste material is utilized, and the environment is not polluted.

Description

The plantation technique of Pleurotus eryngii and Pleurotus geesteranus
Technical field
The present invention relates to planting edible mushroom technical field, be specifically related to the plantation technique of Pleurotus eryngii and Pleurotus geesteranus.
Background technology
Pleurotus eryngii, has another name called pleurotus eryngii, and the fragrance having Semen Armeniacae Amarum because of it and bacterial context plumpness are gained the name such as the mouthfeel of Carnis Haliotidis.It is that successful and edible, medicinal, the dietetic therapy of exploitation cultivation in recent years is in Rare edible fungus new varieties integrally.On market, Pleurotus eryngii product is the most, common such as hundred mountain ancestral's mushroom pickles--Pleurotus eryngii, Pleurotus eryngii extract, instant Pleurotus eryngii fractional pack, the parcel Pleurotus eryngii also having independent packaging etc..Pleurotus geesteranus, formal name used at school Pleurotus geesteranus, originate in South India and look into Mo Sheng.Within 1974, being tamed successfully by fungus scholar Jandiaik.C.L, the nineties in 20th century introduces to Continental Area from Taiwan.The one of Pleurotus ostreatus, belongs to Eumycota, Basidiomycetes, Agaricales, Pleurotaceae, pleurotus on taxonomy.This title of Pleurotus geesteranus derives from Taiwan, be business taste denseer a kind of Pleurotus sajor-caju.It is different from common Pleurotus sajor-caju, and its mushroom body is handsome little, and handle is long 5-6 centimetre, and lid diameter < 3 centimetres, so claiming elegant precious.Pleurotus geesteranus is because of profile clear and melodious, delicious flavour pleasing, fresh and tender, nutritious and obtain person sponging on an aristocrat's favorable comment.The nutritive value of Pleurotus geesteranus is equivalent to milk.Rich in protein in fresh mushroom, amino acid classes is more, and 8 kinds of aminoacid of needed by human are complete.
The yield of Pleurotus eryngii is the highest at present, and the fruiting time is long, and management inconvenience, Pleurotus eryngii waste material cannot use.
Summary of the invention
For solving the problems referred to above, the present invention provides a kind of technique simple, and yield is high, convenient management, it is possible to utilize the Pleurotus eryngii of Pleurotus eryngii waste material and the plantation technique of Pleurotus geesteranus.
Technical scheme
A kind of plantation technique of Pleurotus eryngii, comprise the steps: the preparation of compost, sterilizing cool down, inoculate, hair tube reason and management of producing mushroom;Described compost includes the raw material of following weight portion: wood flour 20-25, Semen Maydis powder 8-12, bean cake 8-12, wheat bran 15-20, corn cob 30-35, pulverized limestone 1-2, calcium carbonate 1-2.
Further, described compost includes the raw material of following weight portion: wood flour 23, Semen Maydis powder 11, bean cake 9, wheat bran 18, corn cob 34, pulverized limestone 2, calcium carbonate 1.
Further, described wood flour natural fermentation, corn cob pulverizer be crushed to grain diameter between 1.2-1.5cm after prewet, the pack of described compost spice i.e. completes the preparation of compost.
Further, the process for preparation of described compost is: the wood flour fermented, corn cob is put in blender according to the ratio of formula, the most again Semen Maydis powder, bean cake, wheat bran, pulverized limestone, calcium carbonate are joined in blender and stirred, in blender, add water move to water account for the 60-68% of compost gross weight, stir, deliver to sack filling machine and carry out dress bag.
Further; described sterilizing cooling step is: packed capping; put into sterilization basket to be placed on sterilizing frame, advance high-pressure sterilizing pot sterilizing, be heated up to pot inner pressure when reaching 1.5 normal atmospheres; steam in autoclave is drained; making pot inner pressure return to normal pressure, be again heated up to 125-126 DEG C, constant temperature is ceased fire after keeping 200-210 minute; boil in a covered pot over a slow fire and take the dish out of the pot to final vacuum in 30-35 minute, sterilizing frame is pushed into cooling workshop and is cooled to less than 30 DEG C.
Further, described bacterium step of sending out is: sends out bacterium and carries out in culturing room, the relative air humidity of culturing room controls below 70%, and ventilation, and during sending out bacterium, the first seven day temperature controls at 22-24 DEG C, from the 8th day, temperature controlled at 23-25 DEG C, incubation is not turned on light, keeps culturing room dark, cultivate 25-30 days, mycelia covers with cultivation bag, is further cultured for after ripening in 7-10 days after covering with cultivation bag.
Further, described management of producing mushroom step is: the bacterium bag sending out bacterium good is moved to mushroom room, is placed on fruiting shelf, opens ventilating system, temperature is adjusted to 12-14 DEG C;After 20 hours, turning on lamp, temperature controls at 16-18 DEG C;Within 3rd day, closing ventilating system, temperature controls at 15-17 DEG C;Within 5th day, open ventilating system, by controlling ventilation time, the concentration of carbon dioxide is controlled at 2000-3000ppm, 6th day starts rudiment, within 8th day, form mushroom flower bud, within 11st day, remove the collar, close lamp, the concentration of carbon dioxide controls at 4000-6000ppm, within 12nd day, the concentration to fortnight carbon dioxide controls at 6000-8000ppm, within 15th day, each cultivation of thin flower bud is wrapped, stay one to two healthy mushroom flower bud, within 16th day, temperature controls at 15-16 DEG C, extraction in 17th day, ripe first extraction is got up, within 18th day, adopt mushroom, ripe mushroom is all gathered.
Further, utilize the plantation technique of Pleurotus eryngii to adopt the technique of the waste material plantation Pleurotus geesteranus produced after mushroom, comprise the steps: that the preparation of compost, sterilizing cool downs, inoculate, hair tube is managed and management of producing mushroom;Described compost includes the raw material of following weight portion: Pleurotus eryngii waste material 40-45, cotton seed hulls 55-60, pulverized limestone 1.5-2.5.
Further, Pleurotus eryngii waste material natural fermentation, Pleurotus eryngii waste material, cotton seed hulls, pulverized limestone are joined in blender and stir, blender adds water move to water and accounts for the 60-68% of compost gross weight, stir, deliver to sack filling machine and carry out dress bag.
Further, described Pleurotus geesteranus management of producing mushroom step is Routine Management step;Described sterilizing cools down, inoculates, it is identical with the corresponding steps in the plantation technique of Pleurotus eryngii to send out bacterium management process.
Beneficial effects of the present invention:
Present invention process is simple, and the yield of Pleurotus eryngii is high, and the pleurotus eryngii fruiting cycle short is 18 days;Pleurotus eryngii waste material can be utilized to plant Pleurotus geesteranus, low cost, and waste material utilizes, free from environmental pollution.
Detailed description of the invention
Embodiment 1
nullA kind of plantation technique of Pleurotus eryngii,By gram weighing raw material: wood flour 230 grams、Semen Maydis powder 110 grams、Bean cake 90 grams、180 grams of wheat bran、Corn cob 340 grams、Pulverized limestone 20 grams、Calcium carbonate 10 grams,Described wood flour is prewetted natural fermentation 1 day in advance,Corn cob pulverizer be crushed to grain diameter between 1.2-1.5 centimetre after prewet,The wood flour prewetted,Corn cob is put in blender according to the ratio of formula,The most again Semen Maydis powder、Bean cake、Wheat bran、Pulverized limestone、Calcium carbonate joins in blender and stirs,In blender, add water move to water account for the 60% of compost gross weight,Stir,Deliver to sack filling machine and carry out dress bag,The polypropylene knuckle plastic bag of packaging bag 18 centimetre of * 36 cm thick of employing 0.05 millimeter,Diameter 38 millimeters,The horn-like collar of high 30 millimeters is joined the plastic plug of non-woven fabrics and is sealed.
After sealing; by packed enter sterilization basket be placed on sterilizing frame; advance high-pressure sterilizing pot sterilizing; it is heated up to pot inner pressure when reaching 1.5 normal atmospheres; steam in autoclave is drained; pot inner pressure is made to return to normal pressure; again 125-126 DEG C it is heated up to; constant temperature is ceased fire after keeping 200 minutes; boil in a covered pot over a slow fire to final vacuum in 30 minutes and take the dish out of the pot; sterilizing frame is pushed into cooling workshop and is cooled to less than 30 DEG C, when temperature is down to below 30 DEG C, the Turnround basket filling bacterium bag is taken off from sterilizing frame, send into conveyer belt and between inoculation, carry out inoculation operation.
In culturing room, hair tube reason is carried out after inoculation, the relative air humidity of culturing room controls below 70%, and ventilation, during sending out bacterium, the first seven day temperature controls at 22-24 DEG C, and from the 8th day, temperature controlled, at 23-25 DEG C, not turn on light in incubation, keep culturing room dark, cultivating 25-30 days, mycelia covers with cultivation bag, is further cultured for after ripening in 7-10 days after covering with cultivation bag.
The bacterium bag sending out bacterium good is moved to mushroom room, is placed on fruiting shelf, opens ventilating system, temperature is adjusted to 12 DEG C;After 20 hours, turning on lamp, temperature controls at 16-18 DEG C;Within 3rd day, closing ventilating system, temperature controls at 15-17 DEG C;Within 5th day, open ventilating system, by controlling ventilation time, the concentration of carbon dioxide is controlled at 2000-3000ppm, 6th day starts rudiment, within 8th day, form mushroom flower bud, within 11st day, remove the collar, close lamp, the concentration of carbon dioxide controls at 4000-6000ppm, within 12nd day, the concentration to fortnight carbon dioxide controls at 6000-8000ppm, within 15th day, each cultivation of thin flower bud is wrapped, stay one to two healthy mushroom flower bud, within 16th day, temperature controls at 15-16 DEG C, extraction in 17th day, ripe first extraction is got up, within 18th day, adopt mushroom, ripe mushroom is all gathered.500 grams of Pleurotus eryngiis are plucked in one packaging bag.
After Pleurotus eryngii is gathered, waste material is used for planting Pleurotus geesteranus, and the compost of described Pleurotus geesteranus includes the raw material of following grams: 450 grams of Pleurotus eryngii waste material, cotton seed hulls 600 grams, pulverized limestone 25 grams.Pleurotus eryngii waste material is prewetted natural fermentation 1 day in advance, Pleurotus eryngii waste material, cotton seed hulls, pulverized limestone is joined in blender and is stirred, adds water move to water and account for the 68% of compost gross weight, stir in blender, delivers to sack filling machine and carries out dress bag.Described sterilizing cools down, inoculates, it is identical with the plantation technique of Pleurotus eryngii to send out bacterium management process.
Management of producing mushroom step is: move on to out in mushroom shed by the bacterium bag sending out bacterium good, and bacteria 3 days is stuffy, moisturizing of spraying water;First tide fruiting: scraping the former base of old strain or hypertrophy, the relative humidity of mushroom house is 92%, keeps 5 days continuously, room temperature 25 DEG C, giving diffused light every day to irradiate, ventilate water spray, and the concentration of carbon dioxide controls at below 1000ppm, 4cm is reached Deng the elongation of mushroom handle, bacteria cover diameter reaches 2cm and sprays with aerosol apparatus when i.e. cap is open and flat, can adopt mushroom, after adopting mushroom after one day, remove old root and some former bases not broken up of charge level, to scraping to fresh compost;Needing to carry out bacterium bag water flood treatment before second tide fruiting, immersion makes bacterium bag increase by 50 grams of water, is then placed in the freezer of 4 DEG C 24 hours stimulating, is taken out of from mushroom house by bacterium bag, carry out illumination, and after mushroom flower bud manifests again, management is with the first tide;Later harvesting is same with the second tidal epoch;Described sterilizing cools down, inoculates, it is identical with the plantation technique of Pleurotus eryngii to send out bacterium management process.
Embodiment 2
nullA kind of plantation technique of Pleurotus eryngii,Raw material is weighed: wood flour 200 grams according to following grams、Semen Maydis powder 90 grams、Bean cake 110 grams、170 grams of wheat bran、Corn cob 310 grams、Pulverized limestone 10 grams、Calcium carbonate 20 grams,Described wood flour is prewetted natural fermentation 2 days in advance,Corn cob pulverizer is prewetted after being crushed to grain diameter 1.2 centimetres,The wood flour prewetted,Corn cob is put in blender according to the ratio of formula,The most again Semen Maydis powder、Bean cake、Wheat bran、Pulverized limestone、Calcium carbonate joins in blender and stirs,In blender, add water move to water account for the 60% of compost gross weight,Stir,Deliver to sack filling machine and carry out dress bag,The polypropylene knuckle plastic bag of packaging bag 18 centimetre of * 36 cm thick of employing 0.05 millimeter,Diameter 38 millimeters,The horn-like collar of high 30 millimeters is joined the plastic plug of non-woven fabrics and is sealed.
After sealing; by packed enter sterilization basket be placed on sterilizing frame; advance high-pressure sterilizing pot sterilizing; it is heated up to pot inner pressure when reaching 1.5 normal atmospheres; steam in autoclave is drained; pot inner pressure is made to return to normal pressure; again 125 DEG C it are heated up to; constant temperature is ceased fire after keeping 200 minutes; boil in a covered pot over a slow fire to final vacuum in 30 minutes and take the dish out of the pot; sterilizing frame is pushed into cooling workshop and is cooled to less than 30 DEG C, when temperature is down to below 30 DEG C, the Turnround basket filling bacterium bag is taken off from sterilizing frame, send into conveyer belt and between inoculation, carry out inoculation operation.
In culturing room, hair tube reason is carried out after inoculation, the relative air humidity of culturing room controls below 70%, and ventilation, during sending out bacterium, the first seven day temperature controls at 22 DEG C, and from the 8th day, temperature controlled, at 23 DEG C, not turn on light in incubation, keep culturing room dark, cultivating 250 days, mycelia covers with cultivation bag, is further cultured for after ripening in 7 days after covering with cultivation bag.
The bacterium bag sending out bacterium good is moved to mushroom room, is placed on fruiting shelf, opens ventilating system, temperature is adjusted to 12 DEG C;After 20 hours, turning on lamp, temperature controls at 16-18 DEG C;Within 3rd day, closing ventilating system, temperature controls at 15-17 DEG C;Within 5th day, open ventilating system, by controlling ventilation time, the concentration of carbon dioxide is controlled at 2000-3000ppm, 6th day starts rudiment, within 8th day, form mushroom flower bud, within 11st day, remove the collar, close lamp, the concentration of carbon dioxide controls at 4000-6000ppm, within 12nd day, the concentration to fortnight carbon dioxide controls at 6000-8000ppm, within 15th day, each cultivation of thin flower bud is wrapped, stay one to two healthy mushroom flower bud, within 16th day, temperature controls at 15-16 DEG C, extraction in 17th day, ripe first extraction is got up, within 18th day, adopt mushroom, ripe mushroom is all gathered.450g Pleurotus eryngii is plucked in one packaging bag.
After Pleurotus eryngii is gathered, waste material is used for planting Pleurotus geesteranus, and the compost of described Pleurotus geesteranus includes the raw material of following grams: 420 grams of Pleurotus eryngii waste material, cotton seed hulls 580 grams, pulverized limestone 20 grams.Pleurotus eryngii waste material is prewetted natural fermentation in advance, Pleurotus eryngii waste material, cotton seed hulls, pulverized limestone is joined in blender and is stirred, adds water move to water and account for the 68% of compost gross weight, stir in blender, delivers to sack filling machine and carries out dress bag.Described sterilizing cools down, inoculates, it is identical with the plantation technique of Pleurotus eryngii to send out bacterium management process.
Management of producing mushroom step is: move on to out in mushroom shed by the bacterium bag sending out bacterium good, and bacteria 2 days is stuffy, moisturizing of spraying water;First tide fruiting: scraping the former base of old strain or hypertrophy, the relative humidity of mushroom house is 92%, keeps 5 days continuously, room temperature 23 DEG C, giving diffused light every day to irradiate, ventilate water spray, and the concentration of carbon dioxide controls at below 1000ppm, 3cm is reached Deng the elongation of mushroom handle, bacteria cover diameter reaches 2cm and sprays with aerosol apparatus when i.e. cap is open and flat, can adopt mushroom, after adopting mushroom after one day, remove old root and some former bases not broken up of charge level, to scraping to fresh compost;Needing to carry out bacterium bag water flood treatment before second tide fruiting, immersion makes bacterium bag increase by 30 grams of water, is then placed in the freezer of 3 DEG C 24 hours stimulating, is taken out of from mushroom house by bacterium bag, carry out illumination, and after mushroom flower bud manifests again, management is with the first tide;Later harvesting is same with the second tidal epoch;Described sterilizing cools down, inoculates, it is identical with the plantation technique of Pleurotus eryngii to send out bacterium management process.
Described above to the disclosed embodiments, makes professional and technical personnel in the field be capable of or uses the present invention.Multiple amendment to these embodiments will be apparent from for those skilled in the art, and generic principles defined herein can realize without departing from the spirit or scope of the present invention in other embodiments.Therefore, the present invention is not intended to be limited to the embodiments shown herein, and is to fit to the widest scope consistent with principles disclosed herein and features of novelty.

Claims (10)

1. the plantation technique of a Pleurotus eryngii, it is characterised in that comprise the steps: the preparation of compost, sterilizing cool down, inoculate, hair tube reason and management of producing mushroom;Described compost includes the raw material of following weight portion: wood flour 20-25, Semen Maydis powder 8-12, bean cake 8-12, wheat bran 15-20, corn cob 30-35, pulverized limestone 1-2, calcium carbonate 1-2.
The plantation technique of Pleurotus eryngii the most according to claim 1, it is characterised in that described compost includes the raw material of following weight portion: wood flour 23, Semen Maydis powder 11, bean cake 9, wheat bran 18, corn cob 34, pulverized limestone 2, calcium carbonate 1.
The plantation technique of Pleurotus eryngii the most according to claim 1, it is characterised in that described wood flour natural fermentation, corn cob pulverizer be crushed to grain diameter between 1.2-1.5cm after prewet, the pack of described compost spice i.e. completes the preparation of compost.
The plantation technique of Pleurotus eryngii the most according to claim 3, it is characterized in that, the process for preparation of described compost is: the wood flour fermented, corn cob is put in blender according to the ratio of formula, the most again Semen Maydis powder, bean cake, wheat bran, pulverized limestone, calcium carbonate are joined in blender and stirred, in blender, add water move to water account for the 60-68% of compost gross weight, stir, deliver to sack filling machine and carry out dress bag.
The plantation technique of Pleurotus eryngii the most according to claim 4; it is characterized in that; described sterilizing cooling step is: packed capping; put into sterilization basket to be placed on sterilizing frame; advance high-pressure sterilizing pot sterilizing; it is heated up to pot inner pressure when reaching 1.5 normal atmospheres; steam in autoclave is drained; pot inner pressure is made to return to normal pressure; again 125-126 DEG C it is heated up to; constant temperature is ceased fire after keeping 200-210 minute, boils in a covered pot over a slow fire and takes the dish out of the pot to final vacuum in 30-35 minute, sterilizing frame is pushed into cooling workshop and is cooled to less than 30 DEG C.
The plantation technique of Pleurotus eryngii the most according to claim 5, it is characterized in that, described bacterium step of sending out is: sending out bacterium and carry out in culturing room, the relative air humidity of culturing room controls below 70%, and ventilation, during sending out bacterium, the first seven day temperature controls at 22-24 DEG C, and from the 8th day, temperature controlled, at 23-25 DEG C, not turn on light in incubation, keep culturing room dark, cultivating 25-30 days, mycelia covers with cultivation bag, is further cultured for after ripening in 7-10 days after covering with cultivation bag.
The plantation technique of Pleurotus eryngii the most according to claim 6, it is characterised in that described management of producing mushroom step is: the bacterium bag sending out bacterium good is moved to mushroom room, is placed on fruiting shelf, opens ventilating system, temperature is adjusted to 12-14 DEG C;After 20 hours, turning on lamp, temperature controls at 16-18 DEG C;Within 3rd day, closing ventilating system, temperature controls at 15-17 DEG C;Within 5th day, open ventilating system, by controlling ventilation time, the concentration of carbon dioxide is controlled at 2000-3000ppm, 6th day starts rudiment, within 8th day, form mushroom flower bud, within 11st day, remove the collar, close lamp, the concentration of carbon dioxide controls at 4000-6000ppm, within 12nd day, the concentration to fortnight carbon dioxide controls at 6000-8000ppm, within 15th day, each cultivation of thin flower bud is wrapped, stay one to two healthy mushroom flower bud, within 16th day, temperature controls at 15-16 DEG C, extraction in 17th day, ripe first extraction is got up, within 18th day, adopt mushroom, ripe mushroom is all gathered.
8. the technique that the plantation technique utilizing the Pleurotus eryngii described in any one of claim 1-7 adopts the waste material plantation Pleurotus geesteranus produced after mushroom, it is characterised in that comprise the steps: that the preparation of compost, sterilizing cool downs, inoculate, hair tube is managed and management of producing mushroom;Described compost includes the raw material of following weight portion: Pleurotus eryngii waste material 40-45, cotton seed hulls 55-60, pulverized limestone 1.5-2.5.
The plantation technique of Pleurotus geesteranus the most according to claim 8, it is characterized in that, Pleurotus eryngii waste material natural fermentation, Pleurotus eryngii waste material, cotton seed hulls, pulverized limestone are joined in blender and stir, in blender, add water move to water account for the 60-68% of compost gross weight, stir, deliver to sack filling machine and carry out dress bag.
The plantation technique of Pleurotus geesteranus the most according to claim 9, it is characterised in that described management of producing mushroom step is Routine Management step;Described sterilizing cools down, inoculates, it is identical with the corresponding steps in the plantation technique of Pleurotus eryngii to send out bacterium management process.
CN201610120006.1A 2016-03-03 2016-03-03 Planting technologies for pleurotus eryngii and pleurotus geesteranus Pending CN105724056A (en)

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CN106892701A (en) * 2017-04-25 2017-06-27 徐州天马敬安食品有限公司 A kind of method that utilization pleurotus eryngii bacteria residue cultivates elegant precious mushroom
CN107853071A (en) * 2017-11-08 2018-03-30 福建省农业科学院农业生态研究所 A kind of method using Chinese pennisetum factory culture pleurotus eryngii
CN110419388A (en) * 2019-08-02 2019-11-08 十堰市农业科学院 A kind of pleurotus eryngii cultivating material and preparation method based on sweet Chinese sorghum pole
CN113317120A (en) * 2021-07-03 2021-08-31 杭州临安鼎新农业科技有限公司 Industrialized pleurotus geesteranus planting process by improving matrix and planting conditions

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CN103430772A (en) * 2013-08-29 2013-12-11 赵广峰 Comprehensive factory-like circulation production method of pleurotus eryngii and common edible mushrooms
CN105130629A (en) * 2015-08-27 2015-12-09 马鞍山市安康菌业有限公司 Efficient pleurotus geesteranus medium prepared from pleurotus mushroom dreg and preparation method therefor

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CN106892701A (en) * 2017-04-25 2017-06-27 徐州天马敬安食品有限公司 A kind of method that utilization pleurotus eryngii bacteria residue cultivates elegant precious mushroom
CN107853071A (en) * 2017-11-08 2018-03-30 福建省农业科学院农业生态研究所 A kind of method using Chinese pennisetum factory culture pleurotus eryngii
CN110419388A (en) * 2019-08-02 2019-11-08 十堰市农业科学院 A kind of pleurotus eryngii cultivating material and preparation method based on sweet Chinese sorghum pole
CN113317120A (en) * 2021-07-03 2021-08-31 杭州临安鼎新农业科技有限公司 Industrialized pleurotus geesteranus planting process by improving matrix and planting conditions

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