anders said:

Idk how to do a poll here, but here's the querstion:

 
 

Do you see any reason -not- to put any of these to grain?  Please explain so I can understand like a 5yo.

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anders said:

How it it, that you are 'amused'?

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Idk better than being screwed

SpaceDawg said:

T2 plates of PE. Should I be worried about the faint growth on the leading edge?



 

 

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anders said:

Alright, so I misinterpreted this as a place to ask questions, and get learned advice, but evidently either the Stars are misaligned, or I was wrong.

My fault.  Thank you, I will use my own ('screwed') judgment and proceed on my own.

God damn...

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anders said:

Ok, pardon me, I misinterpreted this as a place to ask questions, and get learned advice.  But evidently either the Stars are misaligned, or I was wrong.

My fault. 

Thank you, I will use my own ('screwed') judgment and proceed on my own.

God damn...

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anders said:

DV8DUG said:

You're going about this backwards... You don't remove the bad from the good. You remove good and put it on new plate.

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Ok.  But my reasoning is that the green is such a small surface area compared with the good, that it is sensible to remove the bad.  In either case if the bad has sporullated the good is contaminated.

With as jelly-like as this 1% media is it's not possible to lift a whole plate out in one piece withot folding/cross-innocing/breaking/getting air dust all over it.

I considered your input.  We also seem to have different ideas on the nature of myc we select for: mine is fuzzy, yours is rhizo.  This is the nature of science.  The nature of Life.

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LotKid said:

Fartcoin isn't an umbrella term. It's an actual "asset" you can purchase

https://coinmarketcap.com/currencies/fartcoin/

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Because of COURSE it is.

And there's an asset called Shitcoin. I wonder if its white paper is a bit thin
https://coinmarketcap.com/currencies/shitcoin/

Pic VAT, my first every agar plate, a shitty plate, 5 years ago: