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Found 7 results

  1. I’ve let this sit for far too Long in my IC. I’ve actually got a couple of these . I was going to case them but I’m not sure now . Any thoughts ?
  2. This is my first agar Clone from a nice PE cluster. Transfered this over a month ago . The blue piece is the tissue. Is it supposed to look like that ?
  3. Hello, Lots of jars in this grow pinned inviro(was away), had to cut them out, I will leave those out of terrarium just in case(or should I not). Any advice on best practiice for invitro is appreciated. Also besides the massive clusters of invitro, I have two shrooms invitro that were 3 inches long, I'm worried about the green on the cap. Also new to contamination, at least one jar was suspect so I threw it out. Does contamination just ruin the grow or does it make the shrooms dangerous? All jars smelled OK, so maybe I'm safe , all jars also looked good, for the most part. I have 5 jars soaking, will go in terrarium tomorrow, I'm mostly worried about putting a bad jar in the terrarium and infecting the others. Suspect 1, I threw away, if that is bad, how risky is it that it was near the others.
  4. I'm starting this thread partly because I wanted to try out several methods of growing out shrooms. But I am beginning to lose track of which thread some of these belonged to, some of it is a mix. Anyway, I'll try to mostly add comments to this when as I get some results and especially pictures! I'll start with my invitro grows. These were all done w/ pp5 containers, using rye grass seed. I tried variations, left some to fruit as-is, some were cased w/ 50/50+, some were mixed w/ coffee/coir sub, then cased. Here are the 10 containers I have in fruiting right now, 8 of these either have pins or are about ready to harvest. I apologize for the hard to see pics, I did the best I could!
  5. I am going to post my thoughts on the necessary features a microscope needs to have!! COMPOUND MICROSCOPE 1. Oil immersion lens 2. 1000x plus magnification 3. Ocular micrometer eye piece 4. electric light source 5. controls to move stage mechanically 6. both a fine and course focus knob 7. standard interchangeable fitments If I have left anything out please add to the basic list!! Remember this is for the basic beginner microscope. Enjoy! PLEASE READ MZ's post below for other great options. I am going to get what he is talking about for sure!!!!
  6. Eugene


    Hello, my name is Yussif Maskalive. I live in hell and I will be here for quite some time. Some people call me Eugene, but I call myself Eu. I remember being in my home country and picking some shamanic flesh flowers as a child for more rations. When it became clear to me when I ingested the flesh flower I had insight on the world and its workings. I will begin to grow the flesh flower with the help of my friend Stan. Stan is the man. Goo Goo Ga Jube, my friends.
  7. This is a little old school but it works great! This is how it was done before PF tek was around.Prep some grains in whatever size jars you prefer (pints are ok, quart size works better FYI! )Noc up your jar as you would any other grain jar with some MS, agar or LC (agar and LC for quicker results) and then place in IC for appropriate amount of time to become 100% colonized. With MS anywhere from 2-4 weeks, with agar and LC 8-14 days. Once it looks something like this; you are ready to case.Casing can consist of your favorite recipe or straight verm (which is my prefered casing).Once cased place in FC with temps around 70 within a week usually you will see pins.Great fast way to get some prints quickly from a strain that you may not have surplus genetics wise and don't want to take too many chances with losing out with bulk but want bigger and more potent fruits than the PF tek.Invitro growth can be minimized with foil wrapped tightly around the jar or any other creative means you can think of to block light from getting to the sides of the jar. But it usually wont happen too much until you try to get more than one or two flushes and the grains begin to contract from the myc consuming it and creating air flow between the myc and glass. Pics are old but so is the tek, the main thing that matters is that it will get you results easily and with minimal extra steps.
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