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Albrecht - style balancing

Y

YosemiteSam

I used Tom's mix outdoors then had an analysis after the grow. I ended up with a 10:1 Ca:Mg base saturation after all was said and done...like 71% Ca and 7% Mg. edit...I used gypsum but probably could have used some dolomite in there to reduce that ratio a little bit. pH at the end of the grow was 5.9, did not bother a thing.

There was absolutely no puddling on that soil at all.

Brix was a couple of points higher on those plants than any I grow indoors. There was no insect or fungus pressure at all other than some freakin grasshoppers
 

xmobotx

ecks moe baw teeks
ICMag Donor
Veteran
insect pressure seems to be another pitfall avoided when applying high Ca additions; probably not as critical when neem is among the ammendments

Ca seems to be something we can consider like Si for strengthening crops against insect issues
 

Montana

Member
by: Michael Astera

Adsorb vs Absorb

adsorb (ad sôrb, -zôrb), v.t. Physical Chem. to gather (a gas, liquid, or dissolved substance) on a surface in a condensed layer: Charcoal will adsorb gases .

Please note the definition above, taken from my handy dictionary, flower press, and child booster seat, the real hardbound Random House second edition unabridged. It's not absorb, it's adsorb , with a "d". We all know that a sponge absorbs water, a cast iron pot absorbs heat, a flat-black wall absorbs light. None of those gathers anything on the surface in a condensed layer, they soak it right in, they absorb it.

Adsorb is different, because it means to gather on a surface in a condensed layer . This is pretty much the same thing as static cling, like when you take a synthetic fabric shirt out of the clothes dryer and it wants to stick to you. You don't absorb the nylon blouse, you adsorb it. Everyone got that? Good. On to Cation Exchange Capacity.

The Exchange Capacity of your soil is a measure of its ability to hold and release various elements and compounds. We are mostly concerned with the soil's ability to hold and release plant nutrients, obviously. Specifically here today, we are concerned with the soil's ability to hold and release positively charged nutrients. Something that has a positive (+) charge is called a cation, pronounced cat-eye-on. If it has a negative charge (-) it is called an anion, pronounced ann-eye-on. (Both words are accented on the first syllable.) The word "ion" simply means a charged particle; a positive charge is attracted to a negative charge and vice-versa.

Positively charged particles are known as cations. There are two types of cations, acidic or acid-forming cations, and basic, or alkaline-forming cations. The Hydrogen cation H+ and the Aluminum cation Al+++ are acid-forming. Niether are plant nutrients. A soil with high levels of H+ or Al+++ is an acid soil, with a low pH.

The positively charged nutrients that we are mainly concerned with here are Calcium, Magnesium, Potassium and Sodium. These are all alkaline cations, also called basic cations or bases. Both types of cations may be adsorbed onto either a clay particle or soil organic matter (SOM). All of the nutrients in the soil need to be held there somehow, or they will just wash away when you water the garden or get a good rainstorm. Clay particles almost always have a negative (-) charge, so they attract and hold positively (+) charged nutrients and non-nutrients. Soil organic matter (SOM) has both positive and negative charges, so it can hold on to both cations and anions.

Both the clay particles and the organic matter have negatively charged sites that attract and hold positively charged particles. Cation Exchange Capacity is the measure of how many negatively-charged sites are available in your soil.

The Cation Exchange Capacity of your soil could be likened to a bucket: some soils are like a big bucket (high CEC), some are like a small bucket (low CEC). Generally speaking, a sandy soil with little organic matter will have a very low CEC while a clay soil with a lot of organic matter (as humus) will have a high CEC. Organic matter (as humus) always has a high CEC; with clay soils, it depends on the type of clay.

Base Saturation %

From the 1920s to the late 1940s, a great and largely un-sung hero of agriculture, Dr. William Albrecht, did a lot of experimenting with different ratios of nutrient cations, the Calcium, Magnesium, Potassium and Sodium mentioned above. He and his associates, working at the University of Missouri Agricultural Experiment Station, came to the conclusion that the strongest, healthiest, and most nutritious crops were grown in a soil where the soil's CEC was saturated to about 65% Calcium, 15% Magnesium, 4% Potassium, and 1% to 5% Sodium. (No, they don't add to 100%; we'll get to that.) This ratio not only provided luxury levels of these nutrients to the crop and to the soil life, but it strongly affected the soil texture and pH.

The percentage of the CEC that a particular cation occupies is also known as the base saturation percentage, or percent of base saturation, so another way of describing Albrecht's ideal ratio is that you want 65% base saturation of Calcium, 15% base saturation of Magnesium etc. Don't get too hung up on these percentages; they are general guidelines and can vary quite a bit depending on soil texture and other factors.

It's still a little-known fact that the Calcium to Magnesium ratio determines how tight or loose a soil is. The more Calcium a soil has, the looser it is; the more Magnesium, the tighter it is, up to a point. Other things being equal, a high Calcium soil will have more oxygen, drain more freely, and support more aerobic breakdown of organic matter, while a high Magnesium soil will have less oxygen, tend to drain slowly, and organic matter will break down poorly if at all. In a soil with Magnesium higher than Calcium, organic matter may ferment and produce alcohol and even formaldehyde, both of which are preservatives. If you till up last years cornstalks and they are still shiny and green, you likely have a soil with an inverted Calcium/Magnesium ratio. On the other hand, if you get the Calcium level too high, the soil will lose all its beneficial granulation and structure and the too-high Calcium will interfere with the availability of other nutrients. If you get them just right for your particular soil, you can drive over the garden and not have a problem with soil compaction.

Because Calcium tends to loosen soil and Magnesium tightens it, in a heavy clay soil you may want 70% Calcium and 10% Magnesium; in a loose sandy soil 60% Ca and 20% Mg might be better because it will tighten up the soil and improve water retention. If together they add to 80%, with about 4% Potassium and 1-3% Sodium, that leaves 12-15% of the exchange capacity free for other elements, and an interesting thing happens. 4 or 5% of that CEC will be filled with other bases such as Copper and Zinc, Iron and Manganese, and the remainder will be occupied by exchangeable Hydrogen , H+. The pH of the soil will automatically stabilize at around 6.4 , which is the "perfect soil pH" not only for organic/biological agriculture, but is also the ideal pH of sap in a healthy plant, and the pH of saliva and urine in a healthy human.

So we are looking at two new things so far:

1) The Cation Exchange Capacity, and

2) The proportion of those cations in relation to each other: the percent of base saturation (% base saturation) and their effect on pH.

We are also looking at two old familiar things, clay and soil organic matter, and these last two need a bit more clarification.

How Clay and Humus Form

Clay particles are really tiny; I mean really. really tiny. They are so small that they can't even be seen in most microscopes. They are so small that when mixed in water they may take days, weeks, or months to settle out, or they may never settle out and just remain suspended in the water; not dissolved, but suspended. A particle that remains suspended in water like this, suspended but not dissolved, is known as a colloid . Organic matter, as it breaks down, also forms smaller and smaller particles, until it breaks down as far as it can go and still be organic matter. At that stage it is called humus , and humus is also a colloid; when mixed into water humus will not readily settle out or float to the top. Colloids, because they are so small, have a very large surface area per unit volume or by weight. Some clays, such as montmorillonite and vermiculite, have a surface area as high as 800 square meters per gram, over 200,000 square feet (almost five acres) per ounce! The surface area of fully developed humus is about the same or even higher. Other clays have a much lower surface area, and some clays actually have a very low exchange capacity, while humus always has a high exchange capacity.

Mineral soils are formed by the breakdown of rocks, known as the parent material . Heating and cooling, freezing and thawing, wind and water erosion, acid rain (all rain is acid; carbon dioxide in the air forms carbonic acid in the rain), and biological activity all break down the parent material into finer and finer particles. Eventually the particles get so small that some of them re-form, that is they re-crystallize into tiny flat platelets, and become colloidal clay, made up mostly of silica and alumina. These clay particles aggregate into thin, flat sheets that stack together in layers.

Clay "History"


How old a soil is usually determines how much clay it has. The more rainfall a soil gets, the faster it breaks down into clay. Arid regions are mostly sandy and rocky soil, unless they have areas of "fossil" clay. River bottoms in arid regions will often have more clay because the small clay particles wash away easily from areas without vegetation cover. As noted above, clays tend to stick together in microscopic layers. Newly formed clays will often be made up of layers of silica and alumina sandwiched with potassium or iron. On these young clays, the only available exchange sites are on the edges. As the clays age, the "filling" in the sandwich gets taken out by acid rain or soil life or plant roots, opening up more and more negatively charged exchange sites and increasing the exchange capacity. Eventually these clays become tiny layers of silica and alumina separated by a thin film of water. These are the expanding clays ; when they get wet they swell, and when they dry out they shrink and crack deeply. Because these expanding clays have exchange sites available between their layers and not just on the edges, they have a much greater exchange capacity than freshly formed clays. Over millions of years, the space in these expanding clays gets filled back in with hydrated aluminum oxide and they lose their exchange capacity again, this time permanently.

In the southern half of the USA, the age of the clay fraction of the soil generally increases going from West to East. The arid regions, from California to western Texas, are largely young soils, containing a lot of sand and gravel and some young clays without a lot of exchange capacity. The central regions, from West-central Texas and above into Oklahoma, Kansas, and Nebraska, contain well-developed clays with high CEC. Moving East, the rainfall increases, the soils are older, and the clays are generally aged and have lost much of their ability to exchange cations. Across Louisiana, Mississippi, Alabama, and Georgia the clays have been rained on and leached out for millions of years. Their reserves of Calcium and Magnesium are often long gone. The northern tier states, from Washington in the West to Pennsylvania and New York in the East were largely covered with glaciers as recently as 10,000 years ago, which brought them a fresh supply of minerals, and clays of high exchange capacity are common.

Organic Matter and Humus

Regarding soil organic matter (SOM) and humus, obviously any area that gets more rainfall tends to grow more vegetation, so the fraction of the soil that is made up of decaying organic matter will usually increase with more rainfall. Breakdown of organic matter is largely dependent on moisture, temperature, and availability of oxygen. As any of these increase, the organic matter usually breaks down faster. Moisture and oxygen being equal, colder northern areas will tend to build up more organic matter in the soil than hotter southern climates, with one extreme being found in the tropics where organic matter breaks down and disappears very quickly, and the other extreme being the vast. deep peat beds and "muck" soils of some northern states. As always, there are exceptions, such as the everglades of Florida, where lack of oxygen combined with stagnant water have formed the largest peat beds in the world; the area around Sacramento California is another example: there were muck soils 100 feet deep when that delta was first farmed by European settlers.

Ordinary organic matter from the compost or manure pile, or the remains of last years crops, doesn't have much exchange capacity until it has been broken down into humus, and from what we know, the formation of humus seems to require the action of soil microorganisms, earthworms, fungi, and insects. When none of them can do anything with it as food anymore, it has ended up as a very small but very complex carbon structure (a colloid) that can hold and release many times its weight in water and plant nutrients. The higher the humus level of the soil, the greater the exchange capacity. The only way to increase humus in your soil is by adding organic matter and having healthy soil life to break it down, or to add a soil amendment such as lignite (also known as Leonardite), a type of soft coal that contains large amounts of humus and humic acids. [LIGNITE AVAILABLE HERE] Humus and humic acids have an exchange capacity greater than even the highest CEC clays.

OK, lets pull this information together. We have discovered that:

1) Alkaline soil nutrients, largely Calcium, Magnesium, Potassium, and Sodium, are positively charged cations (+) and are held on negatively charged (-) sites on clay and humus.

2) The amount of humus, and the amount and type of clay, determine how much Cation Exchange Capacity a given soil has.

3) We have also discussed the ideal base saturation percentages of these nutrients, approximately:
65% Ca,
15% Mg,
4% K (Potassium),
1-3% Na (Sodium)

4) We have talked a little about the effect of those ratios on soil texture and pH and why they are not hard and fast "rules".

The next step is understanding how the plant, and the soil life, gets those nutrients from the exchange sites, the "exchange" part of the story.

Trading + for +


In the same way that acid rain can leach cations from the soil, plants and soil microorganisms more or less "leach" the cation nutrients from their exchange sites. These alkaline nutrients are only held on the surface with a weak, static electrical charge, i.e. they are "adsorbed". They are constantly oscillating and moving a bit, pulled and pushed this way and that by other charged particles (ions) in the soil solution around them. What the plant roots and soil microorganisms do is exude or give off Hydrogen ions, H+ ions, and if enough of these H+ ions are given off that some of them surround the nutrient cation and get closer to the negatively (-) charged exchange site than the nutrient is, the H+ ions will fill the exchange site, neutralize the (- ) charge, and the nutrient cation will be free of its static bond and can then be taken up by the plant or microorganism.

The way this works specifically with plant roots is that the plant roots expire or breathe out carbon dioxide into the soil. This carbon dioxide (CO 2 ) combines with water in the soil and forms carbonic acid, and the H+ Hydrogen ions from the carbonic acid are what replaces the cation nutrient on the exchange site. The Calcium ion that is held to the exchange site has a double-positive charge, written Ca++. When enough H+ ions surround it that some of them get closer to the exchange site than the Ca++ ion is, two H+ ions replace the Ca++ ion and the plant is free to take the Ca++ up as a nutrient. Simple as that.

Now we move on to how the CEC is measured, and then, what to do with that information once you have it.

Exchange capacity is measured in milligram equivalents, abbreviated ME or meq. A milligram is of course 1/1000th of a gram, and the milligram they are referring to is a milligram of H+ exchangeable Hydrogen. The comparison that is used is 1 milligram of H+ Hydrogen to 100 grams of soil. If all of the exchange sites on that 100 grams of soil could be filled by that 1 milligram of H+, then the soil would have a CEC of 1. One what? One ME, one meq, one milligram of Hydrogen.

Let me repeat that: 100 grams of a soil with a CEC of 1 could have all of its negative (-) exchange sites filled up or neutralized by 1/1000th of a gram of H+ exchangeable Hydrogen. If it had a CEC of 2, it would take 2 milligrams of Hydrogen H+, if its CEC was 120 it would take 120 milligrams of H+ to fill up all of the negative (-) exchange sites on 100 grams of soil.

The "equivalent" part of ME or meq means that other positively (+) charged ions could be substituted for the Hydrogen. If all of the sites were empty in that 100 grams of soil, and that soil had a CEC of 1, 20 milligrams of Calcium (Ca++), or 12 milligrams of Magnesium (Mg++), or 39 milligrams of Potassium (K+) would fill the same exchange sites as 1 milligram of Hydrogen H+.

Why the difference? Why does it take 20 times as much Calcium as Hydrogen? It's because Calcium has an atomic weight of 40, while Hydrogen, the lightest element, has an atomic weight of 1. One atom of Calcium weighs forty times as much as one atom of Hydrogen . Calcium also has a double positive charge, Ca++, Hydrogen a single charge, H+, so each Ca++ ion can fill two exchange sites . It only takes half as many Calcium ions to fill the (-) sites, but Calcium is 40 times as heavy as Hydrogen, so it takes 20 times as much Calcium by weight to neutralize those (-) charges, or 12 times as much Magnesium (Mg++, also a double charge), or 39 times as much Potassium, by weight . (Potassium's atomic weight is 39, and it has a single positive charge (K+), so it takes 39 times as much K+ to fill all the exchange sites, once again by weight . The amount of + charges, the amount of atoms of K+ or H+, is the same.)

What We Have Learned

We have now learned the basics of CEC, cation exchange, in the soil.

1) Clay and organic matter have negative charges that can hold and release positively charged nutrients. (The cations are adsorbed onto the surface of the clay or humus.) That static charge keeps the nutrients from being washed away, and holds them so they are available to plant roots and soil microorganisms.

2) The roots and microorganisms get these nutrients by exchanging free hydrogen ions. The free hydrogen H+ fills the (-) site and allows the cation nutrient to be absorbed by the root or microorganism.

3) The unit of measure for this exchange capacity is the milligram equivalent, ME or meq, which stands for 1 milligram (1/1000 of a gram) of exchangeable H+. In a soil with an exchange capacity (CEC) of 1, each 100 grams of soil contain an amount of negative (-) sites equal to the amount of positive (+) ions in 1/1000th of a gram of H+.

That's it.

Per 100 grams of soil,1 meq or ME=
1 milligram H+ or
20 mg of Calcium Ca++ or
12 mg of Magnesium Mg++ or
39 mg of Potassium K+ or
23 mg of Sodium Na+

Per Acre, 1 meq or ME=
20 lb Hydrogen H+ or
400 lb Calcium Ca++ or
240 lb Magnesium Mg++ or
780 lb Potassium K+ or
460 lb Sodium Na+
 

mad librettist

Active member
Veteran
Sorry for the long copy-paste, I couldn't resist after Mad stated clay is dead......

please don't misquote me, it is sloppy and unfair.

albrecht spun the clay very fast in a fancy watchamacallit to remove all trace of nutrients. that is what I called dead clay. the clay that is on top of some of my no till containers is very much alive and kicking under the living mulch.

I advocate adding clay back to any container mix to a max of 5%. in most cases more like 2% is ideal but with smart pots I go even beyond 5%.

here is a video about that http://www.greenhousegrower.com/video/764
 
Y

YosemiteSam

Even then all he did was spin the clay in a centrifuge until the mechanical force was greater than the ionic bond force stripping the cations off the clay. That does not strip the negative charge off the clay particles.

It still has the ability in the presence of cations for them to reattach...is that dead?

Plus on the earlier question about my math...if you measure by volume the certainly the air is included. And unless your material is completely bone dry then at least some of the water is included also. So my math definitely was not totally correct, but not way off either.
 

mad librettist

Active member
Veteran
yes your math is way off at the conceptual level and you are not figuring the same problem at all.


you call a mix that is 50/50 peat and perlite "50/50 peat and perlite", not x% perlite, y% water, z% air, etc... albrecht's figures show how much water and air are in the soil is and are completely unrelated to recipes for soilless mixes. one is a recipe and the other is an accounting of physical properties of soil in the field.

It still has the ability in the presence of cations for them to reattach...is that dead?

are you intending to have a philosophical discussion or can we just pretend you know what I mean? you think sterile clay is alive?

ok, from now on we will say sterile clay is alive. just so long as we know it's sterile clay everyone can discuss albrecht's findings.
 
Y

YosemiteSam

I respect your knowledge. I read a lot of your posts, find them very informative and follow some of your advice.

I went overboard on the dead clay thing...totally semantics and meaningless. Should have kept my mouth shut...I apologize.

but when you measure by volume (and not weight) there is air involved in that volume, regardless if you wanna talk %s or simply ratios...there is no way around it. cause if you say 50% peat you are actually talking peat plus air...so it is in fact some % of actual peat and some % of air...you cannot avoid that, peat contains pore space and therefore air. and unless it is bone dry it also contains some % of water. so you can say 50/50 peat/perlite by volume...but that is just a shorthand way...cause it is actually x% peat, y% perlite, z% air and q% water...those exact %s will depend on how wet the peat is and exactly how the particle packing of the entire mix works out...Albrecht is saying when you get the Ca:Mg right you get a specific particle packing (cause Ca flocculates clay particles) and that leads to the ideal ratios.

still, it has no real bearing on anyones better understanding of ideal soil. Feel free to have the last word if you like...I will drop it.
 

mad librettist

Active member
Veteran
but when you measure by volume (and not weight) there is air involved in that volume, regardless if you wanna talk %s or simply ratios...there is no way around it. cause if you say 50% peat you are actually talking peat plus air...so it is in fact some % of actual peat and some % of air...you cannot avoid that, peat contains pore space and therefore air. and unless it is bone dry it also contains some % of water. so you can say 50/50 peat/perlite by volume...but that is just a shorthand way...cause it is actually x% peat, y% perlite, z% air and q% water...those exact %s will depend on how wet the peat is and exactly how the particle packing of the entire mix works out...Albrecht is saying when you get the Ca:Mg right you get a specific particle packing (cause Ca flocculates clay particles) and that leads to the ideal ratios.


only albrecht is talking about soil in the field, not a peat mix. His figures are still totally unrelated to a soilless mix recipe. In order to compare the two you need to make a conversion. You could figure out a mix with close to the physical properties he describes, I guess. But the numbers don't compare in any meaningful way.

Ergo, the % humus he gives is unrelated to % by volume EWC used in a mix, and represent ample humus content for growing crops and maintaining healthy soil (ie making sure it doesn't blow away with the wind). The equivalent in a mix is about 10% (9% if you are anal), which is not as rich as most of us run but is still enough to work the magic. If you are managing farmland this is vital because if you are short on humus every % you go up is gonna cost you $$$ and time.
 
I think one issue here is that the experiments were done in the absence of living soil. Albrecht started with inert clay containing no nutes or life at all.

only albrecht is talking about soil in the field, not a peat mix.

which is it mad?

last I checked fields typically had micro and macro life in them.


lul I need to wait and breath more that reads like an insufferable jerk wrote it my apologies.


Edit: So I suppose the only question I have is this why not albrecht for low humus systems like irbs heck this stuff loves to grow in very very low humus environments (gravel)....
 

mad librettist

Active member
Veteran
which is it mad?

last I checked fields typically had micro and macro life in them.


lul I need to wait and breath more that reads like an insufferable jerk wrote it my apologies.


Edit: So I suppose the only question I have is this why not albrecht for low humus systems like irbs heck this stuff loves to grow in very very low humus environments (gravel)....

this isn't so hard!


the experiment albrecht did started with inert as possible clay


the recommendations he gives involve soil in the field


let's chalk this one up to friday night imbibing ok? well, that and not reading the thread sufficiently



and if it were legal, and you were farming it organically, 10% humus would be a great figure to shoot for when growing acres of it.
 
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xmobotx

ecks moe baw teeks
ICMag Donor
Veteran
so it would seem that further research has dated the ratios and there needs to be some adaptation to convert to an indoor mix if we want to apply this research???

thinking that a good exercise when putting together a mix would be to stack ratios and divide just to determine where a specific mix of amendments puts the mix then compare whether its reasonably close to albrechts findings

all purely intellectual unless a major imbalance is found since it really is a case of close enough is good enough

i think doing this the findings will show how diversity especially when using plant based amendments tends to put the ratios into the vicinity of albrechts findings
 
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V

vonforne

well, back on topic

difficult to find simple #s in albrecht's publications but common is suggesting a ratio more like 4-8:1 for cal:mag

seems like 2:1 for cal:phos

and pushed a "how low can you go" approach for N as he advocated legumes rather than amending

the phos:K ratio seems a little confusing by weight its 1:2 and 1:1 by percent

how do people like: N?-P4-K4 Cal8/Mag1 by %

????????????????????????

I did not measure mine that exact..........If I were to guess it would be more like 50 to 50. I used powdered Dolomite lime and a feed store product for chickens. Chicken scratch. Made from crushed oyster shell and coral calcium. It is working well and I did add gypsum in a very small amount.

I have been adding rock dut to the worm bins in very small amounts. For grit as ML stated and its mineral content so it will be available to the plants rather than waiting on the soil microorganisms to break it down over time.

V
 

xmobotx

ecks moe baw teeks
ICMag Donor
Veteran
and that serves to illustrate

you are getting great results w/ your mix showing that this discussion is mostly intellectual

what i wondered was if we can get some refining and improve our results; what i find is we tend to be in the ballpark anyway
 
V

vonforne

and that serves to illustrate

you are getting great results w/ your mix showing that this discussion is mostly intellectual

what i wondered was if we can get some refining and improve our results; what i find is we tend to be in the ballpark anyway

refining.......that is a broad statement considering how we use our soil. The time taken for certain amendments to break down etc. We are in our own words working with a living organism or organisms.

I think to refine the soil matrix would be to study the microorganisms better under a microscope and try and control which ones are the dominant population at any given time. We are doing that as far as bacteria and fungi now. So, to fine tune that we would need to control which ones were dominant.

It is beyond me at this time to do that so I am relying on the soil microorganisms to do it themselves.

V
 

xmobotx

ecks moe baw teeks
ICMag Donor
Veteran
i do mean refining in a broad sense

much like i think comparing ratios to albrechts #s results in finding we have "accidentally" achieved balance by using diversity a'la jaykush; maybe what i try to figure is why what seems like a haphazard approach makes for such good results?

nonetheless i do feel most of us look for some N sources, some P sources, some K sources, then top it off w/ a liming mix; it strikes me that this is key liming mix {viewed as lime agent diversity or cal source diversity; however}

one of the things that really got me curious was noticing how clack used oyster shell, dolo lime and, gypsum; it seemed to put the cal mag ratio closer to albrechts; it got me wondrin if the rest of it might fit in to the puzzle?

i think that where a ratio might seem out of whack; the availability/solubility and/or having charcoal in the mix amounts to correction so to speak

now; i wonder about comparing organic ratios w/ living soil to popular formulas like the rezipe? could be interesting also?

rough values; NPK 6-8-8 cal/mag 5/2 and Su 1% {1/2 strength till 10" tall}

when he doses w/ the koolbloom though; wow
 
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Y

YosemiteSam

You still have to remember that Albrecht ratios were designed for field soil which contains a lot of clay. It is my thinking (possibly wrong) that a lot of his Ca was for flocculating clay particles to get proper packing of particles, proper soil stucture and porosity.

In an open enough soil I believe a 3:1 ratio is best for fertilizing the plant.

Anyway...if you were to measure base cation ratios after each crop eventually you would tweak around until you got those right...at that point maintenance would become pretty easy since each crop should basically remove essentially the same amount from the soil.

The other question I have is that this is designed to produce food with maximum mineral content..is that what we even want in our smoke?

They also claim that nitrates are carcinogenic...and if you think about it nitrates are probably the worst part of even bacon. Makes me question my use of Calcium Nitrate...if I don't wanna eat it do I really wanna smoke it.
 
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