Is anyone playing with VPD based models for conditioning a grow VS relative humidity based target models? The reasoning being the compensation for temp built into the vpd model...thinking .4kpa target with a .1kpa buffer.
I just watched the dehydrator on the cheap video. most of the home dehumidification units Ive looked at only go down to 30%. Does the end up being low enough for storing dried mushrooms or marinated and dried mushrooms (jerky). Any thoughts?
What the Cordy-Cult doesn't want you to know about Cordyceps Militaris Preservation: Peep this very interesting 2024 study that was passed along to me a week or so ago. In essence if you are preserving known mating pairs of CM in their monokaryotic forms (through Deep Freezing/LN/Freeze Drying) and combine once your ready to expand to a round of LC and then fruiting substrate you will never experience "senescence"...as this study points out, our perception of "senescence" might be one thing but in fact in the case of C. Militaris it looks like a dominant monokaryon kicks the other Mon out after a series of expansions essentially rendering a dikaryon, monokaryotic once again.
https://drive.google.com/file/d/1gxqBeIbpvyYTtMGPyu3yiw2vimbfPIfd/view?usp=sharing
A deep dive that follows along this specific protocol is in the works to see if it can be replicated! Stay stoked and share your fungal-finds homies!
-Erik
Hey y'all hope you enjoy our first of many sterile technique videos!! There was a minor yet important detail that wasn't mentioned. So whenever working in front of a HEPA filter be sure to never spray the isopropyl directly at the filter (due to damage). Always keep the spray bottle very slanted or even perpendicular to the filter. Also spraying with a downward angle and close to the object helps prevent the large spread of harmful isopropyl spray. Lastly, with an open culture these rules have to be followed to ensure no damage by isopropyl occurs to our live open cultures. Sorry about that and let me know if any other questions arise!
I was wondering if anyone here has experimented using UV lights to detect bacteria or contamination in general in their setups, spawn, substrate etc.
I saw that blotch is florescent and UV at 365nm would make it glow greenish yellow, so I bought a small UV flashlight and I've been testing inspecting the farm with it. So far I've seen the most use when checking out spawn bags, as I can see weird colored glowing stuff in bags that to the eye seem normal... Anyway it's still under the experimental phase but wanted to share and hear your thoughts!
"Hi everyone!
I’d like to hear your opinions and experiences: Is it better to use more or less nutrients in liquid culture and agar? How can this affect the subsequent growth of mycelium and fruiting bodies? What are the advantages and disadvantages of using higher or lower nutrient concentrations in these media? Thanks in advance for your responses!"
Recently joined the culture club and ordered some genetics. Very impressed with the packaging and quality of the cultures. The golden enoki and lions mane plate cultures are super aggressive. Also tried out the king oyster and reishi grain spawn. So far every thing I have received has performed well on media and grain, moved 40 blocks into my tents this morning, looking forward to seeing the final product and yields. Thank you so much for everything you do, you have a lifetime customer here. Soon I will be trialing out the maitake and 3790 shiitake to compare with my current cultures
LOVE the new Maine Cap n Stem website format! I really appreciate the detailed strain information. Ya’ll are KILLIN it as usual! Thank you! ✌🏻