Proposition 122 said:

What is a "glc jar"?
As in, "I use glc jars for inoculating my qts." -Fahtster

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GenesisCorrupted said:

What should I do about this infection on my big Leaf maple?

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Repeated neem treatment or potassium bicarbonate based spray

Big leaf are especially prone to powdery mildew and other surface fungi.

Mr Piggy said:

GenesisCorrupted said:

What should I do about this infection on my big Leaf maple?

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Repeated neem treatment or potassium bicarbonate based spray

Big leaf are especially prone to powdery mildew and other surface fungi.

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Mr Piggy said:

GenesisCorrupted said:

What should I do about this infection on my big Leaf maple?

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Repeated neem treatment or potassium bicarbonate based spray

Big leaf are especially prone to powdery mildew and other surface fungi.

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Smellyhobbit said:

Proposition 122 said:

What is a "glc jar"?
As in, "I use glc jars for inoculating my qts." -Fahtster

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Grain liquid culture. Above my pay grade, but basically you make myceliated water by adding sterile water to a colonized grain jar, shaking it, and using the resulting fluid as inoculant

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Wow, how deep does this mycology rabbit hole go

tryptkaloids said:

Mr Piggy said:

GenesisCorrupted said:

What should I do about this infection on my big Leaf maple?

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Repeated neem treatment or potassium bicarbonate based spray

Big leaf are especially prone to powdery mildew and other surface fungi.

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What about the red spots? Symptom of something else?

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Dkeppel said:

Hi, Mr. Piggy!



It feels like I haven't seen you post in forever.

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Mub said:

I was about to spawn two jars of x7x+ and two of blue meanie, was getting help from my wife this time And I think we mixed up the jars. Pretty sure one of each went into the tub. I was assuming the x7s were the white ones and BM were the brown ones? Or is it not that easy to tell?

If the x7s were the ones I thought they were they seem a lot different than the B+ I have been growing. I can’t wait to try them. Might even make some micros with them this week.

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boceephus_Jones said:

At what point can I cut an agar wedge and go to grain? Whenever I see any significant amount or once the plate is full?

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Don’t need to wait for the plate to fill out.

Edit: This is a 55mm plate just before I sent it to 4 qt jars.

Wiscoregon said:

Dealing with some kind of Bacteria in my plates, all of my plates, that is showing up as an orange color in the agar when you flip them.

Attempted sequestered plates that never succeeded in bridging the sequester gap, those plates are also 100% w/o contamination.  While the plates where the myc bridged the sequester gap to the other side seem to keep it.

This leads me to believe that the bacteria is stuck in the myco somehow, there's a word for this, maybe someone can remind me.

Thoughts, suggestions, ideas?
I'm seeing improvements w/ each sequestered transfer but just can't seem to shake it entirely.

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