'Alkali soils' are
clay soils with a relatively high exchangeable sodium percentage, a relative high
pH (> 9), a poor soil structure and a low infiltration capacity. Often they have a hard calcareous layer at 0.5 to 1 m. depth.
Akali soils are usually not saline, i.e. the total amount of soluble salts, especially sodium chlorides, is not excessive (ECe < 4 to 8 dS/m).
Alkali soils are also called sodic soils. This does not differentiate alkali soils from saline soils. Saline soils have a high sodicity (i.e. a high sodium content that may be higher than that of alkali soils), but they are not alkali soils and have usually a good infiltration capacity.
In literature, the terms sodicity, alkalinity and basicity are not always clearly differentiated. The term "basic" for high pH is ambiguous as readers might think the word is derived from "basis". Therefore many scientists and authors prefer to speak of alkaline instead of basic.
The notion "alkali soil" is not unambiguous in itself, as the term "akali" corresponds to "sodic".
At present, we will have to live with the given definitions until a new classification comes up.
Causes
The causes of soil alkalinity are natural or they can be man-made.
#The natural cause is the presence soil minerals producing
sodium carbonate (Na
2CO
3) upon
weathering.
#The man-made cause is the application of
irrigation water (surface or ground water) containing a relatively high proportion of
sodium bicarbonates.
Occurrence
The extent of alkaline soils is not precisely known (Brinkman, 1988)
[1] .Important research on alkaline soils has mainly occurred in Central Europe, North India (above the Ganges river) and along the Indus River basin of Pakistan, where alkaline soils occur frequently.
Well known research institutes are:
Indian Central Soil Salinity Research Institute
(CSSRI), Mona Reclamation Research Station, Bhalwal, Punjab Pakistan, and University of Agriculture, Faisalabad, Pakistan.
Agricultural problems
Alkaline soils are difficult to take into agricultural production. Due to the low
infiltration capacity, rain water stagnates on the soil easily and, in dry periods, irrigation is hardly possible. Agriculture is limited to crops tolerant to surface
waterlogging (e.g. rice, grasses) and the productivity is low.
Chemistry
Reference: Handbook 60
[2] .
Soil alkalinity is associated with the presence of
sodium carbonates or (soda) (Na
2CO
3) in the soil, either as a result of natural
weathering of the soil particles or brought in by irrigation and/or flood water.
The sodium carbonate, when dissolved in water, dissociates into 2Na
+ (two sodium
cations, i.e. ions with a positive electric charge) and CO3
= (a carbonate
anion, i.e. an ion with a double negative
electric charge).
The sodium‑carbonate can react with water to produce
carbon dioxide (CO
2), escaping as a gas, and
sodium hydroxide (Na
+OH
–), which is alkaline (or rather basic) and gives high
pH values (pH>9). To understand this reaction, we may consider the water (H
2O) as being partly dissociated into H
+ (
hydrogen) and OH
– (
hydroxyl) ions. In pure, neutral water, the concentration of H
+ and OH
– ions equals 10
–0.7 eq/l each (respectively 10
–7 g/l and 17x10
–7 g/l), a very small concentration.
The pH, being the negative log value of the H
+ concentration in eq/l, is 7. Similarly, the
pOH is also 7.
Each unit decrease in pH indicates a tenfold increase of the H
+ concentration. Similarly, each unit increase in pH indicates a tenfold increase of the OH
– concentration.
In water with dissolved salts, the concentrations of the H
+ and OH
- ions may change, but the sum of pH and pOH remains equal to 14.
Water with excess H
+ ions is called acid (pH < 6), and water with excess OH
– ions is called alkaline or rather basic (pH > 8). Soil moisture with pH < 4 is called very acid and with pH > 10 very alkaline (basic).
The reaction between Na
2CO
3 and H
+O can represented as follows:
2Na
+ + CO3
- - + 2H
+ + 2OH
- --> 2Na
+ + 2OH
- + H
2CO
3
The acid H
2CO
3 is unstable and produces H
2O (water) and CO
2 (
carbon dioxide gas, escaping into the atmosphere). This explains the remaining
alkalinity (or rather
basicity) in the form of soluble
sodium hydroxide and the high
pH or low
pOH.
Not all sodium carbonate follows the above chemical reaction. The remaining sodium carbonate, and hence the presence of CO
3= ions, causes CaCO
3 (which is only slightly soluble) to precipitate as solid
calcium carbonate (limestone). Hence, the calcium ions Ca
++ are immobilized:
2Na
+ + CO
3= + Ca
++ --> 2Na+ + CaCO
3 (solid)

Sodium exchange process
The presence of abundant Na
+ ions in the soil solution and the precipitation of Ca
++ ions as a solid mineral causes the
clay particles, which have negative electric charges along their surfaces, to adsorb more Na
+ in the
diffuse adsorption zone (DAZ, see figure) and, in exchange, release Ca
++, by which their
exchangeable sodium percentage (ESP) is increased as illustrated in the figure:
Na
+ is more mobile and has a smaller electric charge than Ca
++ so that the thickness of the DAZ increases as more sodium is present. The thickness is also influenced by the total concentration of ions in the soil moisture in the sense that higher concentrations cause the DAZ zone to shrink.
Clay particles with considerable ESP (> 16), in contact with non-saline soil moisture have an expanded DAZ zone and the soil swells (
dispersion).
The phenomenon results in deterioration of the
soil structure, and especially crust formation and compaction of the top layer.
Hence the infiltration capacity of the soil and the water availability in the soil is reduced, whereas the surface-water-logging or runoff is increased. Seedling emergence and crop production are badly affected.
Under saline conditions, the many ions in the soil solution counteract the swelling of the soil, so that saline soils usually do not have unfavorable physical properties.
Alkaline soils, in principle, are not not saline since the alkalinity problem is worse as the salinity is less.
Alkalinity problems are more pronounced in
clay soils than in loamy, silty or sandy soils. The clay soils containing
montmorillonite or
smectite (swelling clays) are more subject to alkalinity problems than
illite or
kaolinite clay soils. The reason is that the former types of clay have larger
specific surface areas (i.e. the surface area of the soil particles divided by their volume) and higher
cation exchange capacity (CEC).
Certain clay minerals with 100% ESP (i.e. fully sodium saturated) are called
bentonite, which is used in civil engineering to place impermeable curtains in the soil, e.g. below dams, to prevent seepage of water.
Reference for the the description of the DAZ (officially called
diffuse double layer):
[3] .
Solutions
Reference : Chhabra
[4]
Alkaline soils with solid CaCO
3 can be reclaimed with grass cultures, ensuring the incorporation of much acidifying
organic material into the soil, and leaching of the excess sodium. Deep plowing and incorporating the calcareous subsoil into the top soil also helps.
It is also possible to reclaim alkaline soils by adding acidifying minerals like
pyrite.
Alternatively,
gypsum (
calcium sulphate, CaSO
4. 2H
2O) can also be applied as a source of Ca
++ ions to replace the
sodium at the exchange complex. There must be enough natural drainage to the underground, or else an artificial subsurface drainage system must be present, to permit
leaching of the excess sodium by percolation of
rain and/or
irrigation water through the
soil profile.
To reclaim the soils completely one needs prohibitively high doses of amendments. Most efforts are therefore directed to improving the top layer only (say the first 10 cm of the soils), as the top layer is most sensitive to deterioration of the
soil structure. The treatments, however, need to be repeated in a few (say 5) years time.
It will be important to refrain from irrigation with poor quality water.
The quality of the irrigation water in relation to the
alkalinity hazard is expressed by the following two indexes:
1) The
sodium adsorption ratio (SAR)
[Na
+] {Na
+/23}
SAR = ───────────── = ──────────────
√[Ca
++/2 + Mg
++/2] √{Ca
++/40 + Mg
++/24}
where: [] stands for concentration in meq/l, and {} stands for concentration in mg/l.
It is seen that Mg (
Magnesium) is thought to play a similar role as Ca (
Calcium).
The SAR should not be much higher than 20 and preferably less than 10;
When the soil has been exposed to water with a certain SAR value for some time, the ESP value tends to become about equal to the SAR value.
2) The
residual sodium carbonate content (RSC, meq/l):
RSC = [HCO
3– + CO
3=] ‑ [Ca
+++ Mg
++]
= {HCO
3–/61 + CO
3=/30} ‑ {Ca
++/20 + Mg
++/12}
which must not be much higher than 1 and preferably less than 0.5.
Note that the above expression recognizes the presence of
bicarbonates (HCO
3–), the form in which most carbonates are dissolved.
Leaching sodic saline soils
Saline soils are mostly also sodic (the predominant salt is
sodium chloride), but they do not have a very high
pH nor a poor infiltration rate. Upon leaching they are usually not converted into a (sodic) alkali soil as the Na
+ ions are easily removed. Mostly, the saline (sodic) soils do not need gypsum applications for their reclamation. (See the Chacupe
case study])
References
1. R.Brinkman, 1988. Saline and sodic soils. In: Land Reclamation and Water Management, ILRI publication 27, p.62-68, International Institute for Land Reclamation and Improvement, Wageningen, The Netherlands. ISBN 90 70 26062 1
2. http://www.ars.usda.gov/Services/docs.htm?docid=10158 US Salinity Lab Handbook 60
3. G.H.Bolt (ed.), 1981. Soil chemistry: A. basic elements. Vol 5a, Elsevier, Amsterdam, The Netherlands
4. Chhabra, R. 1996. Soil Salinity and Water Quality. pp 284. Oxford&IBH Publishing Co. Pvt. Ltd., New Delhi (South Asian edition) and A.A. Balkema Uitgevers BC, Rotterdam (edition elsewhere). ISBN 81 204 1049 1.