Soils, their formation, properties, composition, and relations to climate and plant growth in the humid and arid regionsHilgard, Eugene W. (Eugene Woldemar)
Science
Soils, their formation, properties, composition, and relations to climate and plant growth in the humid and arid regions
Hilgard, Eugene W. (Eugene Woldemar)
Soils
_Origin of the Potash Deposits._—The manner in which
this accumulation of potash salts has been formed deserves
explanation. It is abundantly evident that nearly all
deposits of rock-salt thus far known have been formed by the
evaporation of sea-water at times when bays or arms of the
sea were cut off from open communication with the ocean.
The composition of sea-water has already been given and
discussed (chap. 2, p. 26); and by the slow evaporation of
sea-water on a small scale we can quite successfully imitate
the phenomena observed in natural rock-salt deposits. When
sea-water is heated a slight deposit of lime carbonate
(usually containing a little ferric oxid and silica) is soon
formed; and a corresponding thin deposit of ferruginous
limestone is commonly found at the base of rock-salt-bearing
deposits. Next above this we almost invariably find a
deposit of gypsum, sometimes of great thickness; in the
artificial evaporation of sea-water the same thing occurs
so soon as the brine has reached a certain degree of
concentration. It constitutes the major portion of the
“panstone” of salt-boilers. Next above follows a deposit of
rock-salt, at base somewhat mixed with gypsum; its thickness
varies greatly according to circumstances. Above it lie the
potash salts.
In the manufacture of sea-salt by evaporation in shore
lagoons or “saltpans,” the solution remaining after the salt
has been deposited (known as “mother-waters,” or “bittern”),
of course remains on the surface of the salt unless allowed
to drain off, as is done in the process of manufacture. When
not drained off, the water gradually evaporates, and there
remains a saline crust of a composition exactly resembling
that of the upper layers at Stassfurt, containing a large
proportion of potash salts.
If it be asked why the Stassfurt salts are not found
overlying every rock-salt deposit in the world, the answer
is that in a great many cases the concentrated mother-waters
have had an opportunity to flow off from the surface of the
rock-salt by the action of tides, the inflow of fresh water
from the land or from other causes. Their presence therefore
depends upon the fulfilment of accidental conditions not
nearly always realized in the natural evaporation of
sea-water, but which happened to occur on a very large scale
in that portion of the North-European continent.
_Nature of the Salts._—The potash is present in
the Stassfurt salts in the form of complex sulfates and
chlorids containing, besides, sodium, calcium and magnesium
in various proportions and modes of combination. The most
abundant of the potassic chlorid minerals is carnallite, a
hydrous chlorid of potassium and magnesium. The chlorids
characterize chiefly the upper portions of the deposit, the
sulfates the lower.
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