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GROWING GOURMET - Anto2ni.it

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390<br />

GROWTH PARAMETERS<br />

Fragrance Signature: Rich, sweet and farinaceous.<br />

Natural Method of Outdoor Cultivation: Inoculation<br />

of logs or stumps outdoors using<br />

sawdust or plug spawn a la the methods trad<strong>it</strong>ionally<br />

used for Shi<strong>it</strong>ake. This is one of the few<br />

mushrooms which produces well on walnut<br />

logs. Oaks, beech, elm and similar hardwoods.<br />

(The "paper" barked hardwoods such as alder<br />

and birch are not recommended.) Once inoculated,<br />

the 3-4 foot long logs should be buried to<br />

1/3 of their length into the ground, in a naturally<br />

shady location. Walnut is comparatively<br />

slow to decompose due to <strong>it</strong>s dens<strong>it</strong>y, providing<br />

the outdoor cultivator w<strong>it</strong>h many years of<br />

fru<strong>it</strong>ings. A heavy inoculation rate shortens the<br />

gestation period.<br />

Recommended Courses for Expansion of<br />

Mycelial Mass to Achieve Fru<strong>it</strong>ing: This Figure 346. Dr. Andrew Weil in China w<strong>it</strong>h H.<br />

erinaceus forming on oak log.<br />

mushroom, in my experience, requires greater<br />

attention to the details of mycelial development<br />

for the creation of spawn than most other species. The mycelium grows relatively slowly on<br />

nutrified agar media, w<strong>it</strong>h fru<strong>it</strong>bodies often forming before the mycelium has grown to a mere 25<br />

mm. in radius. Furthermore, the transferring of mycelium from agar to grain media using the trad<strong>it</strong>ional<br />

scalpel and wedge technique, results in comparatively slow growth, taking weeks to colonize<br />

unless a regimen of diligent and frequent shaking of the spawn jars is followed.<br />

Hericium erinaceus is a classic example of a species which is stimulated by ag<strong>it</strong>ation in liquid culture.<br />

I wa<strong>it</strong> until primordial colonies form upon the mycelial mat on agar media. At that time, cultures<br />

are cut into sections and placed into an<br />

Eberbach-like stirrer. Once blended, the myceliated fluid, now<br />

rich in the growth hormones<br />

associated w<strong>it</strong>h primordia formation, is expanded by transferring to sterilized<br />

grain filled spawn jars. The result is an explosion of cellular activ<strong>it</strong>y.<br />

Two colonies of mycelium grown out on standard 100 x 15 mm. petri dishes are recommended for<br />

use w<strong>it</strong>h every 1000 ml. of sterile water. Once stirred, 20-50 ml. ofliquid inoculum is poured into every<br />

l<strong>it</strong>er to 1/2 gallonjar. The jars are then thoroughly shaken to evenly distribute the liquid inoculum,<br />

placed on the spawn incubation rack, and left undisturbed. Soon thereafter evidence of mycelial recovery<br />

can be seen, often w<strong>it</strong>h numerous wh<strong>it</strong>e dense spots. These dense wh<strong>it</strong>e spots are s<strong>it</strong>es of<br />

rapidly forming primordia, now<br />

numbering many times over than that which had formed in the original<br />

petri dishes. The spawn jars must be used immediately for further expansion e<strong>it</strong>her into more<br />

sterilized grain or sterilized wood, lest the primordia develop into sizeable fru<strong>it</strong>bodies. Should the latter<br />

occur, further use ofthese spawnjars is not recommended since the developing mushrooms will be<br />

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