Hi Milky,
No offense, but I do have a few questions/comments concerning your statement (the passages in question are underlined):
- How do you know that your primary metabolites are converted to chains? Cause those are often no more solid and/or no longer in the plant sap, hence 'invisible' using plant sap refractometry...
- Why would you want to add 'a wide variety of enzymes' as fertiliser?
- Every good fertiliser contains a 'combo of lots of trace minerals' because they are as important to the plants as vitamins are to us. Basalt, kelp, sea minerals and sulfate salts of the main micros: That part, I don't get... Basalt and kelp may be nice natural sources for minerals, sea salt too but what is 'sea minerals' and why only sulfate salts?
- Also the sentence 'tons of biology to chelate stuff going into the plant to minimize the energy the plant needs to convert stuff' is somewhat weird. What do you mean exactly by that? A plant doesn't use energy to convert something it can't resorb and resorbed minerals, may they be free or bound to a synthetic or natural chelate, are treated the same way. There's always energy used to 'put them in place' if they don't do it by their own; especially chelates have to be metabolised afterwards to get rid of them.
- And finally that one 'controversial cause conventional wisdom is a plant only takes up soluble ions' is wrong. Because many chelates (natural or synthetic) are soluble and modern science has realised that for example metal complexes with humus can still be resorbed and may even have advantages over 'standard' fertilisers. It's just not understood HOW that works .
No offense taken at all. I don't claim to have any real answers, I am learning.
I do not know for a fact longer chains are formed. Other than in plants where tissue testing is done things like protein have formed...that is N plus sugar, right? Or Ca Pectate is a longer chain compound, right?
And yea...a lot of that stuff becomes part of plant and is no longer soluble in the plant. I wonder if Ca influences sap at all. My understanding is it pretty much gets where it is going, forms whatever it forms and that is it. On the other hand something like K mostly stays soluble in the sap, so it greatly influences brix...yet too much k does you no good at all. Plus I wonder if our female plants even have a true sugar sink at all...I am thinking that only happens when a plant is pollinated.
I am looking to get enzyme co factors...does not every enzyme have some metal co factor it needs to form...mostly trace stuff. That is why I like to get a variety of sources in there. And no, not all main traces are through sulfates, obviously the anions cannot be delivered that way...B, Mo for example. I over simplified that.
I actually meant sea salt...I use one that has had the NaCl reduced to about 12%.
I am thinking biology can chelate metals, or complex the single valent stuff, with amino acids and the plant can take that up. There would be energy to break that bond but the plant could then use the amino vs using energy to convert nitrate into amino. No? What I don't know for sure is how much energy does it take to break the bond vs convert nitrate to amino. And I am wondering can you chelate ions with peptides...that could potentially save two energy steps...right?
And, if you have an enzyme that catalyzes any of these reactions you save energy vs not having it right?
That is my thinking anyways. No clue if it is true or not.