tultedspoon said:
Kunta Kente said:
tree frog said: Small correction, Panaeolus bisporus is psuedo-homothallic, so n+n even from a single spore. Not all of these will be compatible mating types, so often they will still cross with another strain (the bisporus strain on the plate, not with like cyans).
And this part is my opinion, not proof. Though it's an informed opinion from reading David Moore's textbook. But I believe that by the time we spawn the war is over. The genetics have already sorted themselves out through the parasexual cycle, and the weaker strains died out. I think this often can happen with pans by t2. Especially in the two spored species. And part of the reason I believe this is because of the break and shake. The substrate acts as a colony, not a bunch of small colonies spread through a large substrate.
So, and again just my opinion, the benefit of cloning isn't in narrowing down the strains. But in epigenetic markers. The cloned strain has learned what conditions to expect. And an isolate from that same plate prior to cloning has not.
Ah didn't know that about bisporus, very cool.
I 100% agree on your "isolated early" statement. Just from the shear fact that we are selecting small sections to take to T1 and T2 likely pares it down to 1-2 genome on T1 and 1 genome on T2.
~~Opinion ahead, (not a TC or even veteran grower, just a bio major and interested)~~ From my reading, I would state this about cloning: You do it to either rescue a culture that you lost the agar of, or to isolate genetics if you had a dirty multispore bulk.
My understanding of epigenetics is the changes are dependent on the current state (current media). So mycellium strongly pushes for tiny changes to optimze for agar while there, and then again separately on grain, and then again separately on bulk.
By nature epigenetic changes are not permanent and can easily be overwritten or drift from favor. So, while in bulk, the colony is NOT optimizing for agar or grain. So, we clone (let's say to into colonies B and C, same genome, same epigenetics.)
Now we are back to agar where bulk doesn't matter at all. We (mycelium) care about only about agar environment performance. B and C will perform essentially identical on agar and grain because those are highly homogenous media. But, while on agar, while on grain, they are again reoptimizing for those medias.
Now back to bulk: B and C are presented with similar but not perfectly identical substrates. Localized sectors (pins, air pockets, and especially corners vs middle) are all different, and so optimization must REOCCUR at those places.
So each and every fruit is constantly optimizing alone. You clone from the middle and it's a different optimization pattern than the side wall, because those are entirely different conditions. Then trying to get a whole tub of the best middle guy or the best side guy would likely both result in simply the same base genome still performing well under relatively similar bulk conditions.
Sorry for again the long write up, I like talking about the background science (as in I'm not saying "NO I'M RIGHT" just saying what I think).
TLDR: combining media specific state optimizations (agar | grain | bulk) and differences in the single bulk environment (the middle is more dry and airy than edges), epigenetics are likely to transient to effectively select for, and performance is much more likely related to the original genomic strength (that should be preserved at the original 'master' T2 for future resampling)
Disclaimer: I'm not an expert I'm thinking there can be some small changes, but I think most is decided from the spores that combine into the mycelium network, and once mycelium branches are formed and venture off and those combinations take place, the changes from then on are more subtle if it's even capable of recomining again and again I don't know. I don't think there's substantial changes as it encounters different media (over time if mycelium was running long distances maybe it could, probably moreso mutations by chance, but the reason it fruits is to make spores for changes too, like the mycelium will run, fruit, spores, whatever takes takes, mycelium runs then fruits again, and then spores again to survive changing environments.
This reminds me I've probably been using not the best prints. I was using recent prints, but I should probably be using older prints when I was finding my specimens more frequently under easier conditions to mimic. I've probably accidentally selected for harder specimens to get bigger flushes from.
I think the mushroom memory may work in such a way that when you take a clone, you are cloning mycelium that will fruit. Not all mycelium is fruiting mycelium, I believe RR said that somewhere. So by taking mycelium from a clone, you know you will have mycelium that is capable of putting out a fruit if conditions are similar. The growth styles for how it performs in spawn are already baked into the genome. I don't think the mycelium has to relearn growing through agar (which actually kind of sounds stupid when you think about it, for reasons people use agar to begin with) or spawn again, the whole lifecycle is already mostly (I say mostly because always possibilities of mutations or selections) determined. The mycelium is so advanced (possibly of alien origin), that it is able to separate from primordia into stem myceliums and cap myceliums, from the root mycelium (something like this I'm close but not exact).
Maybe people are cloning from the middle and the sides, but I think more importantly people are cloning phenotypes or fruiting styles (clusters for big flushes). I don't think master growers are expecting their tubs to have vastly different environments from the middle vs. the sides. There's probably more normal environmental variation that occurs in a regular routine misting.
This is not advice.
|