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	<title>Tutorials/Spores/Prints and Syringes - Revision history</title>
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	<updated>2026-10-24T12:33:46Z</updated>
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		<id>https://wiki.pikespeakmycoleague.org/index.php?title=Tutorials/Spores/Prints_and_Syringes&amp;diff=90&amp;oldid=prev</id>
		<title>imported&gt;Claude: Batch 2: spores, cloning, culture storage, smash tek, drying, local suppliers; convert sources to footnotes</title>
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		<updated>2026-10-22T20:00:00Z</updated>

		<summary type="html">&lt;p&gt;Batch 2: spores, cloning, culture storage, smash tek, drying, local suppliers; convert sources to footnotes&lt;/p&gt;
&lt;p&gt;&lt;b&gt;New page&lt;/b&gt;&lt;/p&gt;&lt;div&gt;Spores are where most grows begin. A single mushroom drops millions of them, each carrying a slightly different mix of its parents&amp;#039; genetics. This page covers collecting spores and turning them into something you can inoculate with.&lt;br /&gt;
&lt;br /&gt;
== Prints, swabs, and syringes ==&lt;br /&gt;
{| class=&amp;quot;wikitable&amp;quot;&lt;br /&gt;
! Form !! What it is !! Good for !! Keeps&lt;br /&gt;
|-&lt;br /&gt;
| &amp;#039;&amp;#039;&amp;#039;Spore print&amp;#039;&amp;#039;&amp;#039; || Spores dropped onto foil or paper || Long-term storage, trading, making syringes || Years, dry and dark&lt;br /&gt;
|-&lt;br /&gt;
| &amp;#039;&amp;#039;&amp;#039;Swab&amp;#039;&amp;#039;&amp;#039; || A sterile cotton swab rubbed across the gills || Quick transfer to agar || Months&lt;br /&gt;
|-&lt;br /&gt;
| &amp;#039;&amp;#039;&amp;#039;Spore syringe&amp;#039;&amp;#039;&amp;#039; || Spores suspended in sterile water || Inoculating agar, LC, or grain || Months, in the fridge&lt;br /&gt;
|}&lt;br /&gt;
&lt;br /&gt;
Spore syringes are convenient, but they can&amp;#039;t be checked for contamination until something grows. &amp;#039;&amp;#039;&amp;#039;Starting spores on [[Tutorials/Agar/Making Plates|agar]] first&amp;#039;&amp;#039;&amp;#039; lets you see what you have, clean it up with [[Tutorials/Agar/Three-Transfers|transfers]], and only then move it to grain.&lt;br /&gt;
&lt;br /&gt;
== Taking a spore print ==&lt;br /&gt;
=== Pick the mushroom ===&lt;br /&gt;
Choose a healthy, mature mushroom whose veil has just torn, exposing the gills, but before the cap flattens and starts dropping spores on its own. A cap that has already dropped spores in the tub will be covered in contamination from the air.&lt;br /&gt;
&lt;br /&gt;
=== Set it up ===&lt;br /&gt;
Do this in a [[Tutorials/Basics/Sterile Technique|still air box]] if you have one; prints pick up whatever is floating around.&lt;br /&gt;
# Wipe a sheet of aluminum foil (or paper, or a glass slide) with alcohol and let it dry.&lt;br /&gt;
# Cut the stem off flush with the cap using a clean, flame-sterilized blade.&lt;br /&gt;
# Set the cap gills-down on the foil.&lt;br /&gt;
# Cover it with a clean glass, bowl, or plastic cup to keep air from moving and to hold in a little humidity.&lt;br /&gt;
# Leave it for 6–24 hours.&lt;br /&gt;
&lt;br /&gt;
=== Collect it ===&lt;br /&gt;
Lift the cap straight up without sliding it. You should see a dark pattern of the gills. Let it air-dry for an hour, then fold the foil over it into a packet, seal it in a labeled zip bag, and store it somewhere cool, dry, and dark.&lt;br /&gt;
&lt;br /&gt;
Label each print with the strain and date. Prints from different strains are indistinguishable once folded.&lt;br /&gt;
&lt;br /&gt;
== Making a spore syringe ==&lt;br /&gt;
=== You&amp;#039;ll need ===&lt;br /&gt;
* A clean print&lt;br /&gt;
* Distilled water, sterilized: pressure cook it in a jar with an injection-port lid (see [[Reference/Pressure Cooking at Altitude|altitude times]]), or boil it for 20 minutes and let it cool covered&lt;br /&gt;
* A sterile syringe and needle&lt;br /&gt;
&lt;br /&gt;
=== Method ===&lt;br /&gt;
# In your still air box, open the print and the water jar briefly.&lt;br /&gt;
# With a flame-sterilized scalpel, scrape some spores into the water. A little goes a long way; a few scrapes will make several syringes.&lt;br /&gt;
# Close the jar and swirl. Let it sit for 12–24 hours so the spores hydrate.&lt;br /&gt;
# Flame the needle, let it cool, and draw the solution up. Re-cap the needle.&lt;br /&gt;
&lt;br /&gt;
Syringe water should look faintly cloudy or have visible dark specks. Clear water may have too few spores; a dark, muddy suspension is more than you need.&lt;br /&gt;
&lt;br /&gt;
== Using spores ==&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;On agar:&amp;#039;&amp;#039;&amp;#039; 1–2 drops in the center of a plate. Look for white growth in 3–10 days, then start [[Tutorials/Agar/Three-Transfers|transferring]].&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;In LC:&amp;#039;&amp;#039;&amp;#039; 1–2 ml per jar. See [[Tutorials/LiquidCulture/Making and Using LC|liquid culture]].&lt;br /&gt;
* &amp;#039;&amp;#039;&amp;#039;In grain:&amp;#039;&amp;#039;&amp;#039; 2–4 ml per quart jar. Slower and riskier than LC or agar.&lt;br /&gt;
&lt;br /&gt;
Spores germinate slowly compared with living mycelium, so expect spore-started cultures to take noticeably longer to get going.&lt;br /&gt;
&lt;br /&gt;
== Swabs ==&lt;br /&gt;
Rub a sterile cotton swab gently across the gills of a freshly opened cap, then return it to its sterile sleeve or a sealed bag. To use it, streak it lightly in a zigzag across an agar plate.&lt;br /&gt;
&lt;br /&gt;
{{Cultivation}}&lt;br /&gt;
[[Category:Tutorials]]&lt;br /&gt;
[[Category:Spores]]&lt;br /&gt;
&lt;/div&gt;</summary>
		<author><name>imported&gt;Claude</name></author>
	</entry>
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