JPH01124327A - Cultivation of mycorrhiza of armillaria matsutake - Google Patents
Cultivation of mycorrhiza of armillaria matsutakeInfo
- Publication number
- JPH01124327A JPH01124327A JP62282600A JP28260087A JPH01124327A JP H01124327 A JPH01124327 A JP H01124327A JP 62282600 A JP62282600 A JP 62282600A JP 28260087 A JP28260087 A JP 28260087A JP H01124327 A JPH01124327 A JP H01124327A
- Authority
- JP
- Japan
- Prior art keywords
- pine
- rock wool
- matsutake
- cube
- cultivation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
- 241000121220 Tricholoma matsutake Species 0.000 title claims abstract description 32
- 241000216654 Armillaria Species 0.000 title abstract 4
- 239000011490 mineral wool Substances 0.000 claims abstract description 27
- 235000008331 Pinus X rigitaeda Nutrition 0.000 claims abstract description 21
- 235000011613 Pinus brutia Nutrition 0.000 claims abstract description 21
- 241000018646 Pinus brutia Species 0.000 claims abstract description 21
- 238000000034 method Methods 0.000 claims abstract description 9
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 239000000463 material Substances 0.000 claims description 4
- 235000000405 Pinus densiflora Nutrition 0.000 abstract description 6
- 240000008670 Pinus densiflora Species 0.000 abstract description 6
- 239000003337 fertilizer Substances 0.000 abstract description 4
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 abstract description 3
- 229910052782 aluminium Inorganic materials 0.000 abstract description 3
- 238000012258 culturing Methods 0.000 abstract description 3
- 239000011888 foil Substances 0.000 abstract description 3
- 230000012010 growth Effects 0.000 abstract description 3
- 239000007788 liquid Substances 0.000 abstract description 3
- 101100491335 Caenorhabditis elegans mat-2 gene Proteins 0.000 abstract 2
- 241000894006 Bacteria Species 0.000 description 7
- 235000018782 Dacrydium cupressinum Nutrition 0.000 description 7
- 235000013697 Pinus resinosa Nutrition 0.000 description 7
- 241000534656 Pinus resinosa Species 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- 241000233866 Fungi Species 0.000 description 5
- 238000011081 inoculation Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 235000001674 Agaricus brunnescens Nutrition 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 230000004720 fertilization Effects 0.000 description 3
- 238000012364 cultivation method Methods 0.000 description 2
- 230000002538 fungal effect Effects 0.000 description 2
- 239000012784 inorganic fiber Substances 0.000 description 2
- 238000005304 joining Methods 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- 230000001954 sterilising effect Effects 0.000 description 2
- 238000004659 sterilization and disinfection Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 1
- 235000005205 Pinus Nutrition 0.000 description 1
- 241000218602 Pinus <genus> Species 0.000 description 1
- 230000005791 algae growth Effects 0.000 description 1
- 230000010065 bacterial adhesion Effects 0.000 description 1
- 239000000378 calcium silicate Substances 0.000 description 1
- 229910052918 calcium silicate Inorganic materials 0.000 description 1
- OYACROKNLOSFPA-UHFFFAOYSA-N calcium;dioxido(oxo)silane Chemical compound [Ca+2].[O-][Si]([O-])=O OYACROKNLOSFPA-UHFFFAOYSA-N 0.000 description 1
- 239000002775 capsule Substances 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 230000021615 conjugation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- 201000010099 disease Diseases 0.000 description 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000002054 inoculum Substances 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000005416 organic matter Substances 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 230000035790 physiological processes and functions Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
Landscapes
- Mushroom Cultivation (AREA)
- Micro-Organisms Or Cultivation Processes Thereof (AREA)
Abstract
Description
【発明の詳細な説明】
本発明は、新素材のロックウール(岩綿)を培地として
マツタケ菌を培養し、別にロックウール栽培によって松
苗を養成し、伸長した松根と培養したマツタケ菌を接合
してさらに同時培養を行なって、人為的に菌根形成をな
さしめることを特長とするマツタケ菌根苗養成方法であ
る。[Detailed Description of the Invention] The present invention involves cultivating Matsutake fungi using rock wool, a new material, as a medium, cultivating pine seedlings through rock wool cultivation, and joining the elongated pine roots with the cultured Matsutake fungi. This is a method for cultivating Matsutake mycorrhizal seedlings, which is characterized by carrying out simultaneous cultivation to artificially cause mycorrhizal formation.
マツタケ菌は生きたアカマツの細根に着生して外生菌根
をつくり栄養を摂取して生きている。The Matsutake fungus grows on the fine roots of living Japanese red pine, creates ectomycorrhizas, and lives by ingesting nutrients.
マツタケ菌は活物寄生菌であるから、松根から切離され
ると弱(カビや雑菌にすぐ犯されてしまう。マツタケ菌
はこの菌の特性と弱さが障害となって、シイタケやその
他の死物寄生菌のキノコのように腐埴性有機物に種菌を
接種して人工栽培することは不可能である。これまで長
年にわたり各種の実験や栽培が試みられてきたが、マツ
タケでは種菌を苗木に接種して栽培する方法はまだ権立
されていない。The matsutake fungus is a living parasitic fungus, so if it is separated from the pine root, it will be easily attacked by mold and other bacteria. It is impossible to artificially cultivate matsutake by inoculating seed fungi into saprophytic organic matter like parasitic mushrooms.Over the years, various experiments and cultivation attempts have been made, but with matsutake, it is impossible to inoculate seedlings with seedlings. The method of cultivation has not yet been established.
4゜
昭和45年ころ長野系のマツタケ出で、マツタケ発生の
シロ(土中の菌糸層)近くのアカマツ若木の根もとから
マツタケが発生し、その根には菌糸が耐着して菌根が形
成されていることが発見され、これがヒントになり昭和
47年ごろから広島県をはじめ各地で試験研究が始まっ
た。マツタケのシロ近くに松苗を植付け、シロが拡張し
て苗木に到着し根に菌根が出来るのを待って、これを堀
取り別の林地に移植してマツタケを増殖しようとするの
が感染画法と言われるものである。4゜ Around 1970, Matsutake appeared in Nagano. Matsutake grew from the roots of young red pine trees near the whites (mycelial layer in the soil) where Matsutake grew, and mycelium became resistant to the roots and mycorrhizae developed. It was discovered that they were forming, and this served as a hint, and experimental research began around 1972 in Hiroshima Prefecture and other locations. The infection method involves planting pine seedlings near the whites of Matsutake mushrooms, waiting for the whites to expand and arrive at the seedlings, and forming mycorrhizas on the roots, then digging up the seedlings and transplanting them to another forest area in an attempt to propagate Matsutake mushrooms. It is called the law.
上記の方法によるこれまでの各地の試験結果では、菌根
が形成された苗の得苗率は極めて低(、移植しても菌が
消滅したり苗木が枯損したりして、技術的な問題点が多
く残されている。新根は菌コqニーの中へ侵入し得ない
が菌糸は根群の中へ侵入し得る。According to the results of tests conducted in various places using the above method, the yield rate of seedlings with mycorrhizae formed is extremely low (and there are technical problems such as the bacteria disappearing or the seedlings dying even after transplanting). Many spots remain.New roots cannot invade into the fungal coqney, but hyphae can invade into the root group.
菌糸がはじめに着生する部位は細根の最先端でもなく根
元でもない。幼令樹の根全体に菌糸が耐着すれば病源菌
が耐着した′状態となる。菌糸をカプセル状にして松根
の一部を包んでも菌根は形成されない。また松根は菌の
着生に対しである種の抵抗力をもっているようであり、
人為的に菌根をつくらせるには接種源の勢いや量、樹勢
や松の生理状態など、マツタケとアカマツの気をあわせ
て歯根を形成させるためにはい(つかの難関がある。The site where hyphae first attach is neither the tip nor the root of the rootlet. If hyphae are resistant to attachment to the entire root of a young tree, the disease-causing bacteria will be resistant to attachment. Mycorrhiza will not form even if the hyphae are made into a capsule and enclose part of the pine root. Pine roots also seem to have a certain resistance to fungal colonization.
In order to create mycorrhizae artificially, there are some difficulties, such as the strength and amount of the inoculum source, the strength of the tree, and the physiological state of the pine, in order for the matsutake and red pine to combine to form tooth roots.
本発明はこのような生理・生態を考慮して10数年来マ
ツタケ菌の培養と接種実験をかさねて来た研究成果をも
とにして、最近新しく製造発売されている無機質繊維で
無菌のロックウールの特性に着目し、(1)ロックウー
ルにマツタケ菌を増殖させ得るか。(2)ロックウール
栽培によって無菌松苗を養成し得るか。という二つの新
しい基礎実験を繰返し行ない創意工夫の末ようやく成功
したのである。この(1)(2)の二つの技術を結合し
てまったく新規で確実な菌根形成法により、菌糸消滅や
松苗の枯損しない菌根苗養成法を発明したのである。The present invention is based on the research results of culturing and inoculating Matsutake fungi over the past 10 years, taking into account the physiology and ecology of these bacteria. Focusing on the characteristics of (1) Is it possible to grow Matsutake fungi on rock wool? (2) Is it possible to grow sterile pine seedlings through rock wool cultivation? After repeating two new basic experiments and ingenuity, they finally succeeded. By combining these two techniques (1) and (2) and using a completely new and reliable mycorrhizal formation method, we have invented a mycorrhizal seedling cultivation method that does not cause mycelium to disappear or pine seedlings to wither.
新素材のロックウールを培地としてマツタケ菌を培養す
るに当っては、ロックウールの物理的、化学的性質を知
る必要がある。In order to cultivate Matsutake fungi using the new rock wool material as a medium, it is necessary to know the physical and chemical properties of rock wool.
A、物理的性質
1、ケイ酸カルシウムを主原料とした無機質繊維である
。A. Physical properties 1. It is an inorganic fiber whose main raw material is calcium silicate.
2、均質で細い繊維(3−7’)で、耐熱性(700℃
)に優れている。2. Homogeneous and thin fiber (3-7'), heat resistant (700℃
) is excellent.
3、孔隙率が高く体積の9096が空気である。3. The porosity is high and 9096 of the volume is air.
4、無菌で品質が安定し、保水性と保温性に優れている
。4. It is sterile, has stable quality, and has excellent water and heat retention properties.
B、化学的性質
さらに、マツタケ菌の培養に当っては、ロックウール培
地に即してマツタケ培養液の組成を考案しなければなら
ない。実験の結果次の如き組成が有効であった。B. Chemical Properties Furthermore, when culturing Matsutake fungi, the composition of the Matsutake culture solution must be designed in accordance with the Rockwool medium. As a result of experiments, the following composition was found to be effective.
特殊培養液の組成
次にアカマツ苗のロックウール栽培については無菌苗の
養成が絶対条件であり、ロックウールは無機質繊維であ
り無菌であるので、他のものよりこの条件をみたしてい
る。松根にマツタケ菌接種以前に他の菌が耐着または感
染していれば画板形成はできない。ロックウールキュー
ての上面中央部に殺菌したアカマツ種子を工種して、ロ
ックウールマット上に乗せる。これをSSシート(吸水
紙の表面をアルミ箔張りとして藻類発生や雑菌耐着防止
と水分発散防止をするためのシート)でロックウールキ
ューブ以下の部分を包み、松苗上部はよく日光に当るよ
うにして松根が伸長してキューブの下面に達するまで施
肥や水分・温度・日照を調節しながら1年ないし2年養
成すれば無菌苗が得られる。Composition of Special Culture SolutionNext, regarding Rockwool cultivation of Japanese red pine seedlings, it is an absolute requirement to cultivate sterile seedlings, and since Rockwool is an inorganic fiber and is sterile, it satisfies this condition better than others. If the pine root is resistant to or infected with other fungi before being inoculated with the Matsutake fungus, it will not be possible to form a drawing board. Spread sterilized red pine seeds in the center of the top of the rock wool cue and place it on the rock wool mat. Wrap the area below the rock wool cube with an SS sheet (a sheet of water-absorbing paper covered with aluminum foil to prevent algae growth, bacterial adhesion, and moisture loss), and leave the upper part of the pine seedling exposed to sunlight. Sterile seedlings can be obtained by growing them for one to two years while fertilizing and controlling moisture, temperature, and sunlight until the pine roots grow and reach the bottom of the cube.
本発明は上記の二つの技術を結合してまったく新規で確
実な菌根形成法により、菌糸消滅や松苗の枯損しない菌
根苗養成法を完成したのである。本発明によって得られ
た菌根菌をマット性のままマツタケ種苗としてアカマツ
林地に植付ければ、枯損も消滅もな(生長して、植付後
の肥培管理良好なる場合は3〜4年後の短期間に子実体
が発生するというマツタケ栽培の革命的な技術進歩であ
る。上述の如く本発明は最新素材のロックウールを用い
てマツタケ菌とアカマツ苗を同時培養するものであり、
1年間の中間培養によってロックウールマットに検板と
ともに生長増殖したマツタケ菌は菌根を形成して容易に
雑菌に犯されない強勢なものとなっており、培養菌は弱
いという定説をくつがえしたのみならず、学問的にも菌
根形成条件の一部が解明されたと言える。本発明によっ
てマツタケ種苗の生産は実用化の段階に入り、マツタケ
人工栽培が可能となった。The present invention combines the above two technologies and uses a completely new and reliable mycorrhizal formation method to complete a mycorrhizal seedling cultivation method that does not cause mycelium to disappear or pine seedlings to wither. If the mycorrhizal fungi obtained by the present invention are planted in a red pine forest as a mat-like seedling of matsutake, it will not wither or disappear (if it grows and the fertilization management after planting is good, it will not die after 3 to 4 years). This is a revolutionary technological advancement in matsutake cultivation in which fruiting bodies are generated in a short period of time.As mentioned above, the present invention uses rock wool, the latest material, to simultaneously culture matsutake fungi and red pine seedlings.
Matsutake fungi, which grew and multiplied on rock wool mats along with test plates through one year of intermediate culture, formed mycorrhizae and became strong enough to not be easily attacked by bacteria, overturning the established theory that cultured fungi are weak. From an academic perspective, it can be said that some of the conditions for mycorrhizal formation have been clarified. With the present invention, production of matsutake seeds and seedlings has entered the stage of practical use, and artificial cultivation of matsutake has become possible.
以下本発明の実施例を図面につき述べる。Embodiments of the present invention will be described below with reference to the drawings.
第1図はアカマツのロックウール栽培装置である。栽培
槽(1)の中にロックウールマット(2)を置き、その
上にロックウールキューブ(3)をのせ、上面中央部の
位置(4)に殺菌したアカマツ種子を丁稚する。マット
両側の底部(5)に液肥を流し、アワせてロックウール
マットの水分を25〜30%に調節する。液肥はハイポ
ネックス100倍液を施用した。稚苗は過湿により徒長
しやすいので肥培管理には注意を要した。Figure 1 shows a rock wool cultivation device for red pine. A rock wool mat (2) is placed in a cultivation tank (1), a rock wool cube (3) is placed on it, and sterilized Japanese red pine seeds are seeded at a position (4) in the center of the top surface. Pour liquid fertilizer into the bottom (5) on both sides of the mat and stir to adjust the moisture content of the rock wool mat to 25-30%. A 100x solution of Hyponex was applied as liquid fertilizer. Young seedlings are prone to elongation due to excessive humidity, so care must be taken in fertilization management.
第2図はアカマツ苗養成状況を示すもので、工種後1〜
2年経過した松苗(6)の成育状況である。根はマット
に達する。破線(7)は接種及び接合する際にロックウ
ールキューブとともに検板を横に切断する部位を示す。Figure 2 shows the cultivation of Japanese red pine seedlings.
This is the growth status of pine seedlings (6) after two years. The roots reach the mat. The broken line (7) indicates the part where the test plate is cut laterally together with the rock wool cube during inoculation and bonding.
接種時に検板を切断することは重要な措置であって菌糸
を活着しやす(する条件の一つである。切断したキュー
ブの下部は捨てる。アカマツは糖菓植物であって温室栽
培には不向きであるから温室内の過乾防止、日照調節、
夏季の高温障害防止、時々室外に出すなど肥培管理には
工夫と苦労を要した。Cutting the test plate at the time of inoculation is an important measure and is one of the conditions that makes it easier for mycelia to take root.The lower part of the cut cube is discarded.Pinus fulva is a confectionery plant and is not suitable for greenhouse cultivation. Because of this, it prevents over-drying in the greenhouse, controls sunlight,
It took a lot of effort and ingenuity to manage the fertilizer, such as preventing heat damage in the summer and occasionally letting the plants outside.
第3図は種苗を接種する箇所を示すものである。菌糸を
接種する際にはロックウール培養液(A液)を含んだ培
地ニスプランソイル(10)を置く。ニスプラン培地の
調製はニスプランソイルにA液をじゅうぶん含ませた後
に水分25%まで脱水し、高圧釜により120°Cl2
O分間の温熱殺菌を行なった。ロックウールマット上に
10ffの厚さに置き、その上に切断した苗付きキュー
ブの上半分を乗せる。この時培地上面の片側の位置(1
1)に、別にあらかじめ口径30朋試験管を用いB液で
培養した菌糸コロニーを接種する。菌令は30日位の勢
いのよいものを試験管1本分を使用した。キューブの上
面と苗木の根元はアルミホイル(8)で被覆するととも
にキューブとマットをSSシート(9)で包む。接種及
接合後は冷暖房設備のある温室に収容して管理培養を読
け、床温は冬期は16〜17°Cとし夏期は26°C以
下とした。床温30’C以上になれば菌糸は衰弱するこ
とが多く失敗する。Figure 3 shows the locations where seeds and seedlings are inoculated. When inoculating mycelia, a medium Nisplan Soil (10) containing Rockwool culture solution (Solution A) is placed. To prepare Nisplan medium, soak Nisplan soil sufficiently with Solution A, dehydrate it to 25% moisture, and boil it in a high-pressure cooker at 120°Cl2.
Heat sterilization was performed for 0 minutes. Place it on a rock wool mat to a thickness of 10 ff, and place the top half of the cube with seedlings on top. At this time, the position on one side of the top surface of the medium (1
In step 1), a mycelial colony previously cultured in Solution B is inoculated using a 30-diameter test tube. One test tube of vigorous bacteria, about 30 days old, was used. The top surface of the cube and the base of the seedling are covered with aluminum foil (8), and the cube and mat are wrapped with an SS sheet (9). After inoculation and conjugation, they were kept in a greenhouse with heating and cooling equipment for controlled cultivation, and the bed temperature was kept at 16-17°C in winter and below 26°C in summer. If the bed temperature exceeds 30'C, the hyphae will often weaken and fail.
第4図はウールマットに新根とともに菌糸も伸びて菌根
(12)が形成された状態を示す。接種及接合後1年間
は温室内で温度、照度、施肥な′ど注意深く管理して検
板と菌糸増殖をはかり1年後の4月に菌根形成を確認し
て、あらかじめ手入れをして発根と集根を促しておいた
アカマツ林地に植付ける。植付けに用いる覆土は滅菌上
が必要である。滅菌上は赤玉土8、ピートモス1、バー
ミキュライト1の容積比で混合調製し、土中の雑菌をお
さえるため酸度はやや高<PH4,5とする。Figure 4 shows a state in which mycelium has grown along with new roots to form mycorrhizas (12) on the wool mat. For one year after inoculation and joining, temperature, illuminance, fertilization, etc. are carefully controlled in a greenhouse, and the growth of mycelia is measured by inspection of plates.In April one year later, mycorrhiza formation is confirmed, and the seeds are taken care of beforehand. Plant in a red pine forest where roots and root collection have been encouraged. The soil used for planting must be sterilized. For sterilization, mix and prepare a volume ratio of 8 parts Akadama soil, 1 part peat moss, and 1 part vermiculite, and keep the acidity slightly high < PH4, 5 to suppress bacteria in the soil.
その土中へ菌根は5〜7月にかけて生長し9月にも増殖
して除々にシロを造成していった。The mycorrhizae grew into the soil from May to July, and continued to multiply in September, gradually creating a shiro.
Claims (1)
を培養し、別にロックウール栽培によって松苗を養成し
、伸長した松根と培養したマツタケ菌を接合してさらに
同時培養を行なって、人為的に菌根形成をなさしめるこ
とを特長とするマツタケ菌根苗養成法。Matsutake fungi were cultivated using rock wool, a new material, as the ground, pine seedlings were cultivated separately through rock wool cultivation, and the elongated pine roots and cultured Matsutake fungi were joined together for further simultaneous cultivation. A method for cultivating Matsutake mycorrhizal seedlings, which is characterized by allowing mycorrhizal formation.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62282600A JPH01124327A (en) | 1987-11-09 | 1987-11-09 | Cultivation of mycorrhiza of armillaria matsutake |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP62282600A JPH01124327A (en) | 1987-11-09 | 1987-11-09 | Cultivation of mycorrhiza of armillaria matsutake |
Publications (1)
Publication Number | Publication Date |
---|---|
JPH01124327A true JPH01124327A (en) | 1989-05-17 |
Family
ID=17654615
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP62282600A Pending JPH01124327A (en) | 1987-11-09 | 1987-11-09 | Cultivation of mycorrhiza of armillaria matsutake |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH01124327A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996033602A1 (en) * | 1995-04-28 | 1996-10-31 | Grodania A/S | A method for the production of fungi |
-
1987
- 1987-11-09 JP JP62282600A patent/JPH01124327A/en active Pending
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996033602A1 (en) * | 1995-04-28 | 1996-10-31 | Grodania A/S | A method for the production of fungi |
US5888803A (en) * | 1995-04-28 | 1999-03-30 | Grodania A/S | Method for the production of mushrooms |
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