Humisolve-ion14™ is the only humate with Soluble Silica, Crucial to Plant health and high yield in Rice and cotton crops!

The usual method of making liquid or dry soluble humates is to extract in an alkaline solution which does not solubilize silica to the silisic acid form required by plants  . However, in our technology it turns in amorphous silica into  sodium and potassium salts of monosilicon acids. These connections, as has appeared, play major role in stimulation of development of plants especially such as rice and cotton. We add addtional silicicacid to our process making Humisolve-ION14 our high soluble silica humic acids product.
See information on the importance of silicon below:
 

From 'Soil Conditions and Plant Growth 10 th. edition E.W.Russell


H. F. Birch' found that, for a group of East African soils, the most efficient method of predicting the response of wheat to a phosphatic fertiliser was to determine the amount of water-soluble silica in the soil, or better still, the amount of silica soluble in I per cent citric acid; for the response decreased linearly with increases in the amount of silica extracted, up to certain level, after which there was no response to phosphate. This result does not have universal application, and is probably restricted to soils which contain their phosphate associated with sesquioxide films.
 
 

Silicon and plant growth


Crops differ considerably in the amount of silicon they take up, but little systematic work has been done on the normal level of silicon in different plants. Grasses and cereals normally have over I per cent of SiO, in their dry matter, and most dicotyledons under I per cent. H. W. Dougal' has deter-
mined the silicon content of several hundred samples of grass and foliage of bushes and trees belonging to forty-seven families and growing in the drier areas of Kenya, and found that the silica content of grasses varied from I to over 10 per cent of the dry matter, with contents of between 2 and 5 per cent being common, while most other plants had silica contents below I per cent and many below 0-2 per cent. Coming to British crops, Table 2-1 on p. 24 shows that cereal straw commonly contains between 10 and 15 kg of silicon per ton while clover, beans and root crops remove only a few kilo-
grams per hectare.
Plant roots take up their silica as silicic acid. It is possible that the amount taken up by most gramineous crops is equal to the amount of silicic acid present in the water the roots absorb, so that the greater the amount of water transpired, the greater their uptake of silica.' Dicotyledonous crops on the other hand take up much less silica than is present in the water their roots take up, often only about 5 per cent, and L. H. P. Jones and K. A. Handreck 4 consider that crimson clover (T. incarnatum), the plant they studied, trans-
located a constant proportion of the silica that reached the roots to the tops, so again, the greater the transpiration the greater the silica content of their tops.
But the validity of these generalisations is uncertain for uptake both by the gramineous crops and the dicots appears to be a metabolic process since enzyme inhibitors, such as sodium azide and dinitrophenol, will cause a reduction in silica uptake without causing a corresponding reduction in ranspiration.' Many varieties of rice 2 and barley will also take up more silica than is carried to the roots by mass flow and dicots, which take up much less silica than comes to the roots by this process, may have a concentration of silica in their xylem sap that is appreciably greater than in the soil solution. Thus, Barber and Shone found that broad beans (Viciafaba) had a silica concentration in their sap five times greater than in the solution bathing their roots.
Grasses and cereals have much of their silica content present as a continuous film, either of a hydrated opal or of some silica-organic complex beween the walls of contiguous cells, and if the organic matter of the cell wall is oxidised away carefully the opal films show up the fine structure of the fibrils forming the wall very clearly.' Grasses and cereals also often possess small cells which are filled with opal. These silica structures break down when dead grass leaves or cereal straw decompose in the soil or are burnt to g' ive the opal phytoliths which are a characteristic feature of grassland soils.
An adequate supply of silica is essential if grasses and cereals are to give a good yield, for it increases the strength and rigidity of their cells. Thus it helps rice leaves to have a more upright habit under conditions of high nitrogen manuring, which may increase the rate of photosynthesis per un' it area of land.' It increases the oxidising power at the surface of rice roots, probably by increasing the rigidity of the walls of the aerenchyma or gas channels within the plant. It is also essential for a good seed set in some varieties of rice, but its mode of action is still unknown .5 It has the same type of action in some dicots, for stinging nettles (Urtica dioica) lose their power of stinging if grown in a silica-free medium, presumably because silica is necessary for hardening their stinging hairs .6 Silica also increases the tolerance of some crops to high levels of available soil manganese for reasons that are not fully understood, but it prevents the manganese in the leaf becoming concen-
trated in a number of spots, which then become necrotic;' and in the case of padi rice allows a greater oxygen supply to the root surface, ensuring a more rapid oxidation of manganese within or just outside the root.
An adequate supply of silica to the cereals will thicken those cell walls on which it is deposited, and this may have a number of desirable consequences. An adequate silica supply reduces the tendency of a cereal to wilt during the initial stages of drought, probably because of the reduced permeability to water or water vapour of the walls of the leaf epidermal cells. There is also evidence that plants adequately supplied with silica have increased resistance to some pests and diseases. Thus, an adequate silica content may increase the resistance of some cereals to powdery mildew (Erysiphe graminiv) 1 and of rice to blast (Pyricularica oryzae),' and to some stem borers, such as Chilo suppressalis,' of sorghums to central shoot fly (A theraqone indica)' and wheat to hessian fly (Mayetiola destructor).'
The use of silica fertilisers, in the form of either soluble silicates, or of calcium silicate slags is still very restricted. Slags are used on some padi rice soils low in soluble silica, which in addition to increasing the pH of the soil are also said to increase the silicic acid concentration in the soil solution. Silicates also increase the yield and sugar content in the juice of sugar-cane growing on soils low in soluble silica.' Silicate fertilisers can, however, increase crop yields for quite other reasons, for they increase the availability of soil phosphate to the crop, presumably by displacing phosphate absorbed on sesquioxide surfaces. This is illustrated in Table 24.1 1 for barley on Hoos-
field at Rothamsted, which shows that a dressing of 450 kg/ha of sodium silicate annually is still increasing the yield of the no-phosphate plots after a century of use. The effect is unlikely to be due to the sodium in the silicate as the source of nitrogen is sodium nitrate, and the plots receiving potash also receive I 10 kg/ha of sodium sulphate. It is probably another example showing that the concentration of water-soluble silicic acid and of phosphate are not two independent quantities in soils, but are closely linked since their solubilities are controlled by the sesquioxide and, in particular, the aluminium hydroxide surfaces.


TABLE 24.11 Effect of silicates on the growth of barley. Hoosfield, Rothamstedsilica barley


References
 IH. F. Birch, J. agric. Sci., 1953, 43, 229, 329; P. K. Garberg, E. Afr. Agric. For. J., 1970, 35, 396.
 2 With V. M. Drysdale and P. E. Glover, E. Afr. Wildlij@ J., 1964, 2, 86.
 3 L. H. P. Jones and K. A. Handreck, Pi. Soil, 1965, 23, 79.
 4 Aust. J. biol. Res., 1967, 20, 483. Silicon 637I
 D. A. Barber and M. G. T. Shone, J. exp. Bot., 1966, 17, 569.
 I E. Lowig, Pflanzenbau, 1937, 13, 362. F. Wagner, Phytopath, 1940, 12, 427.
 2R. J. Volk, R. P. Kahn and R. L. Weintraub, Phvtopath., 1958, 48, 179.
 3A. Djamin and M. D. Pathak, J. econ. Entoni., 1967, 60, 347.
 4B. W. X. Ponnaiya, J. Madras Univ., 1951, 21 B, 203.
 5B. S. Miller, R. J. Rcbinson et al., J. Econ. Ent., 1960, 53, 995.
 6A. S. Ayres, Soil Sci., 1966,101, 216. Y. W. Y. Cheong and P. Halais, Exp. Agric., 1970,6,99
 7R. A. Fisher, J. @qric. Sci., 1929,19, 132. 0. Lemmermann, Ztsch.,Pflanz. Du@q., 1929,13A,
28.
 2A. Okuda and E. Takahashi, The mineral Nutrition o Rice, International Rice Research
Institute, 1965, ch. 10.
 3For some excellent photographs of these films see L. H. P. Jones, A. A. Milne and S. M. Wadham, PI. Soil, 1963, 18, 358.
 4S. Yoshida et al., Pi. Soil, 1969, 31, 48.
 7J. Vlamis and D. E. Williams, PI. Soil, 1967, 27, 13 1; PI. Physiol., 1957, 32, 404.