I think this is to do with how some stems are hollow… I wanted to do a test on a plant that was further in flower so have injected a tangie that is probably 3-4 weeks from finished… This is also hollow stemmed and there is no back pressure when injecting…
I guess the unknown is how is the silver that fills up the hollow center then distributed through the plant… I wanted to do this because it makes it much easier to see how the ethylene ‘blocking’ works at this stage… and what I can see is that the bud sites within 6 inches of the injection have basically had all growth and development of buds at these locations has ‘frozen’… Basically the same as it does if you spray a plant later in flower…
I am trying a non hollow stemmed plant now, and am still waiting to see if this makes it more difficult to get the correct dosage to where it’s needed. I fully expect this process will take a bit of refinement if it turns out to be reliable…
So everyone I did a few more tests using this approach… I used a couple of NYD/OGK fems, one of them grown in coco, the other in a small dwc setup… I whacked these up twice to see if it made any difference.
So this is one that is sitting in dwc… it started out with pistils and these have pretty much all become balls… this one was more fleshy so injection was easier.
So this is an Tangie that I wanted to do a test on to see if the silver might speed up reveg times… mostly because I want a cut from this pheno and had left it way way too long… so this is only just over one week after having the tops cut off and being put back in 18/6, already there is new tips growing and by another week I should be able to take cuts from it… that’s a pretty fast turn around for reveg in my experience, so I am pretty stoked about this use of the silver as well…
Plants have a vascular system, and while the concentration of silver that spreads throughout might not be great enough to reverse the entire plant there will be traces for sure.
I wouldn’t risk it.
That is kind of the conclusion I’m assuming as well. I suppose without some pretty advanced testing like a mass spectrometer to verify the content/lack of, on a non reversed bud from said plant one may never know with certainty.
I thought most from seed runs were just for seed rather than smoke? I wouldn’t wanna chance it personally. Planning on reversing a rainbow kush. (I’ve not forgot about the seed run I’ve just been having issues in life and grow) but this seems a good method. Do you remove the plant you pollinate from flower room or can you leave them in there. Don’t wanna risk a crop but I’ve got a few more plants than usual this run.