|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
SonomaFungi’s first stab (Grow Log) 1
#28624777 - 01/17/24 04:06 PM (10 days, 15 hours ago) |
|
|
Hey, everyone.
Figured I’d start a grow log to document my first stab at mushroom cultivation - the good, the bad, and the ugly. Huge thanks to those who chimed in on my other two threads and helped get me to where I am (even if I’m not quite where I want to be).
So far I’ve: * Poured about 15 MEA plates (Petri dishes). I kept two out at ambient temp in a previously unused ziplock bag (no parafilm). Both control plates show single colonies trichoderma - possibly introduced when I removed the plates from the still air box and put them into the ziplock while exposed to ambient air.
* (1/11/24) Inoculated 3 plates with Golden Teacher and 3 plates with B+. The B+ plates are shown on photos below. They’ve got some widespread discoloration that seems to be bacterial, but has not changed or expanded since it first showed up. The B+ plates are also starting to show some little clumps of white fuzzy growth - possibly mycelium, possibly mold. I’m he golden teacher plates are a mess - some of what looks like bacteria, and nothing that looks good.
* While in my SAB inoculating the plates, I also inoculated 6 PF Tek jars with GT and 6 with B+. The B+ jars are starting to show some rapid mycelium growth. GT jars have some growth that I can see under magnification but not with my eyes alone. I think ALL of my jars are too wet, despite following the PF Tek (2:1:1, verm:BRF:water).
So that’s where I’m at. Please feel free to share your thoughts/critiques/suggestions/etc. All pics were taken today, roughly 1 week after inoculation.
Cheers!
phot









Edited by SonomaFungi_707 (01/17/24 04:08 PM)
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
My PP5 “Slime” cups and micropore tape arrived from Amazon. 🤣 Soon there will be a bunch of little agar plates waiting for their shot at glory.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Here’s another photo of one of my B+ plates.
It looks like my spores germinated on/in the large tan-colored bacterial colony (if that’s what it is?). The bacterial colony (?) has not grown or changed color or anything since it first showed up shortly after inoculation.
If I let this mycelium grow out into the clean area of the plate a little more, can I go ahead and cut some out for a transfer? Or should I just consider this mycelium toast since it literally grew right out of a pool of bacteria?
I’ve read that water agar might be helpful in a situation like this. What do you think?
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
|
Hey, SF!
Hope those jars are colonizing well!
The PP5 slime cups you got seem legit. I bought some sauce containers that had "formed" lids (i.e. not flat) and it made it very difficult to see what was going on inside. Yours appear much better!
Not sure what your particular motivation is for using the slime cups instead of standard petris (I was attracted by a smaller size and cheaper unit cost). If it's to do no-pour agar, it looks like you're on the right track with the PP5 containers. If it's for similar reasons to mine, I found some 60mm petris that were comparable to some of the slime containers. Instead of parafilm, I've been using a roll of cling wrap that I cut into 1-inch rolls.
Quote:
SonomaFungi_707 said: ...
I’ve read that water agar might be helpful in a situation like this. What do you think?

I made water agar for the first time in my most recent batch, and I transferred a pretty clean sample to it to see how the mycelium grows. I'll take some pictures and share here when there's something to show!
Keep in mind that I'm a newcomer to this hobby, but I would probably take a transfer from the leading edge to another nutrient plate, then to water agar. My thinking is that you still want as clean of a transfer as possible before taking to water agar, since the mycelium will still need to utilize the nutrient agar transfer wedge to make new mycelium to search for more food.
I'm very curious about cleaning cultures with water agar and haven't come across a lot of great info, so I'd love if anyone can drop some knowledge!
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: OctopusDisco]
#28626266 - 01/18/24 05:44 PM (9 days, 14 hours ago) |
|
|
Hey, Octopus. My jars are actually looking great! (To me, anyway!)
The Golden Teacher jars are starting to come to life, too, which is neat.
About those slime cups… I’m actually going to return them to Amazon and swap them for the screw top type (like the “holy grail” no-pour, but possibly not the exact same product). The slime cups are just too much of a PITA to open. You have to break the seal on one side, then slide your finger all the way around to break the rest of the seal before the lid will finally pop off. Just too much fuss for working in a cramped SAB…
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Quick update… Roughly 11 out of 12 jars seem to be doing great, as far as I can tell. The B+ are colonizing much faster than the Golden Teacher, but they’re starting to pick up the pace. One B+ jar doesn’t look great - I think it ended up way to wet, possibly due to some water seeping in during the PC cycle. It’s colonizing, but just looks really wet…
Here’s a pic of what the B+ jars look like today. Seems like a mix of tomentose and rhizo growth going on, huh?
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
I also made a batch of 20 no-pour agar plates using “holy grail” type screw top containers and roughly following the steps for using foil instead of that nifty Christmas cookie container.
I’ll take some pics when I pull them out, but I already know they won’t be “perfect”. Added a few drops of blue food coloring to the agar/malt mix while I was stirring it on the stove…. Let’s just say that you DO NOT want to use plant-based food coloring. It immediately formed a bunch of little bluish black flecks rather than dissolving and turning the whole solution blue. Oh well… I doubt it will be a problem aside from just looking funky.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Alright! I went ahead and transferred some mycelium from my germination plates into some freshly made HG agar containers. I’ve got two HGs with B+ and two with Golden Tiger.
Love how clear they are! You can see the little agar chunk I transferred.
Edited by SonomaFungi_707 (01/22/24 08:01 PM)
|
mycoloking
Mycologist Newbie


Registered: 01/01/24
Posts: 46
Last seen: 2 days, 13 hours
|
|
Quote:
SonomaFungi_707 said: Alright! I went ahead and transferred some mycelium from more germination plates into some freshly made HG agar containers. I’ve got two HGs with B+ and two with Golden Tiger.
Love how clear they are! You can see the little agar chunk I transferred.

Looking Great! I just did my first PDA Dishes last night, super stoked it worked out!
Good luck on the agar plate!
-------------------- Hoping to grow some great mushies with some TLC, Tender Loving Care!
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
Re: SonomaFungi’s first stab (Grow Log) [Re: mycoloking]
#28631563 - 01/22/24 10:35 PM (5 days, 9 hours ago) |
|
|
Nice work, SF Those agar containers are pretty rad. Glad you found the solution that works for you! What nutrient source did you use?
The last B+ jar you posted definitely reminds me of what mine looked like. Weird request, but when you birth it, will you report back on how it smells?
|
fiddle_head
I'm not the dude, guy



Registered: 08/05/08
Posts: 1,877
Last seen: 14 minutes, 4 seconds
|
|
always love seeing new names and faces and new grow logs on here. dont be a stranger and let us know if you need any help. keep up the good work frien
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: fiddle_head]
#28631905 - 01/23/24 09:17 AM (4 days, 22 hours ago) |
|
|
Thanks for the replies!
The agar mix I used was 10 grams of light malt extract, 10 grams of agar agar, and 500 ml of water. I also added a couple drops of what turned out to be plant based blue food coloring (fail!) - it just turned into little flecks of solid material when I mixed it into the hot agar solution. Shouldn’t hurt anything, but definitely didn’t dye the plates blue. 🙄
I’ll definitely report back on how these jars smell when I crack them open. So far they don’t really smell like anything, but I’m trying not to fiddle with them too much so it’s not like I’m sticking my nose right up to the holes or anything.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Dang… Lost a jar to trichoderma (maybe two, TBD). I’m sure this was caused by me handling these things too much, which probably caused some dry vermiculite (plus trichoderma spores) to drop down along the edge of the jar. Lesson learned - next time I’ll do my best to leave them the F alone.
I took the jar outside and opened it up for a post-mortem exam. I was surprised to find that the mycelium was mostly around the outside. The inside of the cake was firm, moist, and pliable - almost like the texture you’d get if you mixed vermiculite with clay. I’m not sure if this is normal, or caused by my particular ingredients or mixing ratio. Maybe my vermiculite is too coarse, which could lead to a higher percentage of brown rice flour when measuring by volume? It just seemed very “gluey” inside, for lack of a better word - not a lot of void space for airflow.
I might try grinding up my own brown rice next time - maybe a coarser grind will avoid the gluey/clay-like texture.
Live and learn, huh?
Good thing I stopped by the hardware store yesterday and bought another dozen half pint jars. 🤣 I think I’ll put some micropore tape over the holes immediately after injecting this next round… I also have some fine vermiculite coming in the mail. I think that will help with my water content issue.




Edited by SonomaFungi_707 (01/23/24 12:00 PM)
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
|
Quote:
SonomaFungi_707 said: I’m sure this was caused by me handling these things too much, which probably caused some dry vermiculite (plus trichoderma spores) to drop down along the edge of the jar. Lesson learned - next time I’ll do my best to leave them the F alone.
Bummer about the jar! 100% that's the reason mine got contaminated too: overhandling that caused pieces of vermiculite to fall down the sides.
Quote:
SonomaFungi_707 said: I might try grinding up my own brown rice next time - maybe a coarser grind will avoid the gluey/clay-like texture.
Any particular reason you want to do BRF/verm cakes instead of putting agar directly to whole brown rice? I just used some whole brown rice for grain spawn and it was extremely easy.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: OctopusDisco]
#28632099 - 01/23/24 12:30 PM (4 days, 19 hours ago) |
|
|
I don’t have any clean mycelium growing on agar yet, so that’s the main reason I’m not going to grain jars yet. I’m working on agar stuff in parallel, but will probably just do another batch of PF Tek jars in the meantime to keep this hobby rolling along and hopefully get some fruits before too long. Once I’ve got fruits, I will do some cloning to agar.
I’ve got two more unused syringes (plus a small amount of leftover B+), and won’t need NEARLY the full volume for agar work. Might as well noc up another round of PF Tek jars, huh?
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Here’s a photo of that one jar I mentioned that’s obviously too wet/mucky. It’s growing, but there are big wet patches that don’t seem to be colonizing.
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
|
The splotchy growth is concerning. Are there any portions of the cake that do not look like that?
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: OctopusDisco]
#28632317 - 01/23/24 04:37 PM (4 days, 15 hours ago) |
|
|
It’s all splotchy like that. The mix is just so wet and mucky it’s sticking to the sides of the jar. All 12 of my jars seem on the wet/mucky side, but this one is EXTRA - must have gotten some water in there somehow during the PC cycle. I separated this jar from the others, and I’m just gonna keep an eye on it - you know, for science. 🤓 I don’t plan to mix this one into my shoeboxes when the time comes.
We’ll see what happens!
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
|
Yeah, I'd definitely keep this one separate from the others. When the time comes, this one might be a good candidate for fruiting directly from the jar. I've seen people add a top layer and attach a plastic bag to the jar with a rubber band.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: OctopusDisco]
#28632354 - 01/23/24 05:17 PM (4 days, 14 hours ago) |
|
|
That’s kinda what I was thinking, actually. Bag it up and see what happens.
|
BrokenHeart
Stranger



Registered: 02/27/23
Posts: 127
Last seen: 2 hours, 58 minutes
|
|
My first pf jars were too wet, I added too much water, I put them aside for a few weeks then top fruited them like this. They looked alot like your last pics.
 I just de lidded, placed over feild capacity coir on top, and put them in a tub with an inch of water. Got fruits from failure.
Edited by BrokenHeart (01/23/24 05:35 PM)
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: BrokenHeart]
#28632380 - 01/23/24 05:46 PM (4 days, 14 hours ago) |
|
|
Nice! Making the most of what you’ve got - I like it.
|
AlexandrDughin
Explorer

Registered: 10/30/23
Posts: 35
Loc: Europe
Last seen: 3 hours, 9 minutes
|
|
I am on my first grow, and for me it was much much easyer to use popcorn instead of other grains/ brf. - i used clean mycellium grown on agar and not went the brf method.
For me, the grain jars failed 2 times - too dry and compact / too wet - molds - bacteria - same goes for agar : too wet and mycellium fails to grow on it and bacteria flourishes.
Switching to popcorn seems to have solved all the moisture problems easly, as getting the corect moisture level is very important, and i find it is much more easy to get that level on popcorn at least for me.
I wish you all the best and a successfull harvest
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
I might give popcorn a try at some point, but I haven’t gotten to the point of clean mycelium on agar yet. That pretty much leaves me with PF Tek and practicing with agar, for now.
I’ve got some agar in the works right now, and I’ve still got two untouched syringes (plus some dregs from my first round). My goal is to have some clean mycelium growing on agar but the time I run out of spore solution. That way I never have to F with buying syringes again.
|
AlexandrDughin
Explorer

Registered: 10/30/23
Posts: 35
Loc: Europe
Last seen: 3 hours, 9 minutes
|
|
With agar, starting from nature harvested semilanceata i managed to get some clean cultures(5) growing after 2 months +- and maybe up to 40 petri dishes and 2 transfers..
with cleaner, imported cubensis took 1 transfer and again up to 40 dishes to get maybe 10 clean ones.
Using a stil air box.
I think, with agar, making lots of them will help, like: start with 20. 18 will fail expand the 2 good ones back to 20 about half will fail again etc... and spawn the spore solution on just water agar, so that bacterias have a harder time growing.
In the space of 2 months of experimenting i had : black mold, cobweb, at least 4 different bacteria types, yeasts, thricoderma etc
It's an uphill,constant fight against contaminants 
But once you manage to isolate a clean culture on agar, the rest is much easyer !
I wish you the best of luck
Ps: I put my current experiment in my signature, you will find there some photos of agar under microscope ( spores, initial phase of grow , contaminants etc ), i hope it can help you a bit.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Thanks for sharing!
Yeah, it does seem like it’s a numbers game - start WAY more than you hope will succeed, at least until you have your methods dialed in.
I plan to use an inoculation loop to apply much less spore solution per plate for my next round, and I think that will up my chances of success.
I’m anxiously waiting to see some growth on the agar to agar transfers I just did yesterday morning. I grabbed the very outside leading edge of the mycelium (furthest from the bacterial contamination) - hoping I got enough mycelium there to keep growing, but we’ll see!
Hey, at least is a lot cheaper than all my other hobbies! The inevitable failures along the way shouldn’t sting toooo much. 🤪
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
😁I woke up this morning to find some nice white fuzz starting to show on the little chips of agar I transferred over to no-pour plates. And still zero contamination visible. Woohoo!
The bad news is I lost another PF jar to trichoderma. I’m down to four B+ jars (one lost to trich and one waterlogged) and five GT jars (one lost to trich).
So now I’m in a bit of a predicament… I’ve got my jars colonizing in Sterilite shoeboxes with the lids cracked, mostly just to minimize the amount of ambient dust that might settle on them (one shoebox for B+, one for GT).
Do I check my jars 1-2 times a day to try to catch any other trich contaminated jars before they explode with spores inside the shoebox? Or do I leave them be to minimize any disturbances that could cause more of my dry verm filter layer to spill down the gaps that are forming between the “cake” and the side of the jar?
I’m leaning toward slowly/gently checking each jar once a day, but open to suggestions. I’m also considering wiping down the lid of each remaining jar with ISO, just to knock down any trich spores that might have escaped from the contaminated jars.
I’ll definitely be adding micropore tape to my next round of PF jars for an added layer of protection. Switching to fine vermiculite should give me a more effective filter layer, but also the smaller bits will have an easier time sneaking down the sides of the jar once the cake starts pulling away from the edges of the jar.
Edited by SonomaFungi_707 (01/24/24 09:43 AM)
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
I went ahead and checked the jars again this morning. No more trich that I could see, but lost two more GT jars to golden yellow bacterial goo at the bottom of the jars right below inoculation holes - looks like the same stuff that showed up in the agar plates I first inoculated with GT syringe. I suspect the remaining GT jars will have similar bacteria issues, since it seems like that syringe was contaminated right from the start.
It’s all good. I’m in no hurry and I’m learning from my mistakes. I’m optimistic about cleaning up these cultures on agar so I can move on to quart jars of grain. 
|
AlexandrDughin
Explorer

Registered: 10/30/23
Posts: 35
Loc: Europe
Last seen: 3 hours, 9 minutes
|
|
You have sealed jars ( with lid on ) inside a shoebox ?
From my limited experience : Once you get contamination inside the jars it's *almost game over for those jars. For a contaminated jar : - take some parts of the good colonized bits transfer those bits to agar so you can clean them and get a new culture. ( if access to new spores is an issue ) - if the contamination is kinda isolated on one side, you could try and cut the contaminated part and put the rest in fruiting. ( if the rest is fully colonized )
Keep in mind that this is what i am currently doing with parts of my lost grain jars. (currently i have some pinnings on a petri dish where i salvaged some micellium from a contaminated jar, 2 more small boxes that are about to pin, also salvaged, and a bigger tray that has black mold all over the bottom and it seems that might be pinning shortly...)
I jave no experience with brf cakes, but they might push trough and give some fruits anyway.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Thanks for the tips!
I am going to let the bacterial jars do their thing for a while and see what happens. I already dumped the ones with trich outside and washed the jars - I don’t want those spore bombs anywhere near my work space.
I’ve got both strains working on agar already, so probably won’t bother with dissecting the PF jars and trying to pull some clean mycelium. Then again, maybe I will just for the heck of it. 🙄
Edited by SonomaFungi_707 (01/24/24 10:34 AM)
|
AlexandrDughin
Explorer

Registered: 10/30/23
Posts: 35
Loc: Europe
Last seen: 3 hours, 9 minutes
|
|
Here is my attempts at recovering contaminated jars. ( i am doing this while my clean jars get to colonize, as an experiment, because, as you said : why not ? )
Recovered mycellium on petri dishes

Trying to spawn a highly black mold contaminated grain jar
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Yikes. I hope I never have to deal with black mold. I wish you luck!
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Ok…. Trying to plan ahead here in terms of agar work and (hopefully soon) moving on to grain. In particular, I’m trying to decipher how many agar transfers might be needed. For simplicity, let’s just consider the B+ for now (I’m at the same place with the GT).
So I started with an ugly bacterial plate inoculated with a spore syringe. Some spores germinated, and mycelium “escaped” from the bacterial goo to a clean part of the plate. I then grabbed two bits of clean mycelium and transferred to clean plates. I labeled the new plates as “B+: T1A” (B+, transfer 1, plate A) and “B+: T1B” (B+, transfer 1, plate B).
Now it appears I’ve got mycelium growing on plates T1A and T1B - so far no visible contamination.
Here’s what I’m thinking…
Once T1A and T1B have grown to roughly quarter sized, I will transfer bits of mycelium from each T1 plate into three new plates. The labeling gets confusing to me at this point, but in essence I will have six T2 plates (three from one T1 and three from the other).
Assuming these six T2 plates all grow out OK, I will pick the four that look best and send them to grain. The remaining two will be stored in the fridge for use later.
This is, of course, the best case scenario. Quantities will be adjusted based on reality. 🤪
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Came up with a labeling convention. (To be fair I partially stole it from some other random thread…)
I’m thinking (or at least hoping) that I’ll be able to send B+:AA, B+:BB, etc (or others of the same generation) to grain.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
|
Oooo…. I think my first round of agar to agar transfers was a success! So far I see nice fuzzy growth and zero contamination. 😁
Assuming these “T1” plates continue to grow w/o contamination, would it make sense to let them grow a little more, transfer a little to new plates, then put the rest of this “T1” agar straight to grain?

Edited by SonomaFungi_707 (01/25/24 12:55 PM)
|
mycoloking
Mycologist Newbie


Registered: 01/01/24
Posts: 46
Last seen: 2 days, 13 hours
|
|
I really like your work here! I am kinda trying the same thing with my B+ spore syring...
Good luck
-------------------- Hoping to grow some great mushies with some TLC, Tender Loving Care!
|
OctopusDisco
Quabity Assuance


Registered: 12/10/23
Posts: 51
Loc: In a bear hole
|
|
Hell yeah, Sonoma! Those look great!!
Quote:
SonomaFungi_707 said: ... Assuming these “T1” plates continue to grow w/o contamination, would it make sense to let them grow a little more, transfer a little to new plates, then put the rest of this “T1” agar straight to grain?
I'm curious to hear what people say on this. Assuming the culture is clean, I'd say send it to grain whenever you want. Additional transfers of a clean culture will have the effect of "isolating" genetic strains, but I'm not really convinced that we can pick fruiting winners based on plates alone. I'd love to test the hypothesis someday.
|
SonomaFungi_707
Stranger
Registered: 12/24/23
Posts: 80
Last seen: 12 hours, 55 minutes
|
Re: SonomaFungi’s first stab (Grow Log) [Re: OctopusDisco]
#28634999 - 01/25/24 08:52 PM (2 days, 10 hours ago) |
|
|
Yeah, I have no delusions of picking “winning” genetics just by looking at the mycelium on a plate. 🤣 I just want to confirm it’s clean and see what its got!
I just bought a 25 lb sack of white proso millet today. $12.99 at the local feed store. Not bad!
A large part of why I’m doing this is just that I’m a scientist at heart and I love experimenting. So I’ll probably try some of this T1 mycelium in some grain and see what happens. This is fun. 😁
|
|