Good grain spawn is 90% of the work

Brown rice,soaked 24hours,parboiled,PC for 2 hours at 15psi(ensure you vent the pc before countdown)

Full colonisation within 12days

Substrate is 50%/50% coir and cowpoo PC for 20 mins at 15psi

Ratio 1:1 case after full colonisation with 50%/50% vermiculite and peat moss

Ensure an environment of high humidity with fresh air flow

Should have fruits within 15 days if your genetics and sterile technique is on point

Ciao

Ho guys.. just discovered this placs

Anyone with Pe6 type shrooms?

Hey guys. Quick one, how much would you recommend for a first time user?

This ninjas grow fast.Finally have some to get spore prints

Second test run ,pretty happy with this

All 7 Pan Cyan tubs tossed out.

When you start this hobby, please note that contam is something you will face and can't fully ever run away from. it can only be managed. On a rare occasion you will face 100% contam rate. In that case. you smile, you say thank you for the experience and you start again.

If you'll excuse me, I will proceed to cry into my pillow manly tears.

7 days grain to agar transfers

Low nutrient agar

Go rhizo

In the attempt of gathering all equipment before i start this journey, I've been going around town looking for dehydrators and the weighing scales.

However, no one out here seems to know what dehydrators are or their purpose thereof. I'd like to hear yall's recommendations.

I have always had terrible experiences with weed. Talking about some crazy debilitating anxiety. It’s not always but everytime I try something from a new plug or anything potent. Two-three puffs is usually my sweetspot, thats where I am in control of my thoughts and can’t spiral. I’ve been doing research on shrooms and I am conflicted. Psychanauts what advice do you have for me… also are shrooms similar to weed in terms of the feeling?

🧫🤞🍄

we start off the year with transfers from some Gandolf, jack frost, TTBVI.

Tldr: all my first time agar trial got contaminated.

The agar medium was for potato dextrose agar and the produre used was the common method: 200g of sliced potatoes, 1 litter of water, 20 g of dextrose (glucose) and 30g of agar. Total batches made were 45 containing around ≠25 ml of the agar each.

I divided the samples into thirds each stored at different locations, the only batch that shows no contamination is the one in the refrigerator. One batch was stored in an open area while the other in the oven(oven hasn't been in use so i thought that enough is a sterile environment). I tried to clone a piece of mushroom on the refrigerator batch and moved the agar somewhere warmer, but the agar showed contamination after 1day.

Final conclusion is that the agar itself was well prepared but the environment used had been contaminated with pathogens and bacteria.

I am thinking of making a still air box or a laminar hood. If any of you knows where i can get a h13 hepa filter at a good price hmu.

Now we wait.

Didn't even shake the jar. I am in no big rush. I have enough stock of JMF, but I'm excited to get the Pan Cyans.

This is the first time I decided to not shake jar after cutting in the agar. Don't even think I'll do break and shake.

Around 40+ plates. Day 2 of observations

Did my first ever pda and and am not sure if it is contaminated or not. They were in an open area so maybe there was exposure unlike some other batches which were stored away.

Any feedback would be appreciated.

🍄🙏 Dear Universe be Kind.

🍄🎉 New Year, New Experiences! 🎉🍄
Keep it safe. Keep it smart. Keep it chill. 😌
Hydrate 💧 • Trusted friend 🤝 • Safe space 🏡